NZ616399B2 - Fruity flavored cocoa products and processes for producing such cocoa products - Google Patents
Fruity flavored cocoa products and processes for producing such cocoa products Download PDFInfo
- Publication number
- NZ616399B2 NZ616399B2 NZ616399A NZ61639912A NZ616399B2 NZ 616399 B2 NZ616399 B2 NZ 616399B2 NZ 616399 A NZ616399 A NZ 616399A NZ 61639912 A NZ61639912 A NZ 61639912A NZ 616399 B2 NZ616399 B2 NZ 616399B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- cocoa
- nibs
- product
- beans
- liquor
- Prior art date
Links
- 244000299461 Theobroma cacao Species 0.000 title claims abstract description 340
- 235000009470 Theobroma cacao Nutrition 0.000 title claims abstract description 326
- 238000000034 method Methods 0.000 title claims description 70
- 239000000843 powder Substances 0.000 claims abstract description 100
- 150000001875 compounds Chemical class 0.000 claims abstract description 99
- 239000000796 flavoring agent Substances 0.000 claims abstract description 55
- 235000019634 flavors Nutrition 0.000 claims abstract description 51
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 claims abstract description 44
- INAXVXBDKKUCGI-UHFFFAOYSA-N 4-hydroxy-2,5-dimethylfuran-3-one Chemical compound CC1OC(C)=C(O)C1=O INAXVXBDKKUCGI-UHFFFAOYSA-N 0.000 claims abstract description 42
- 235000019868 cocoa butter Nutrition 0.000 claims abstract description 25
- 229940110456 cocoa butter Drugs 0.000 claims abstract description 24
- 229940100595 phenylacetaldehyde Drugs 0.000 claims abstract description 22
- WDAXFOBOLVPGLV-UHFFFAOYSA-N ethyl isobutyrate Chemical compound CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 claims abstract description 18
- 244000046052 Phaseolus vulgaris Species 0.000 claims description 71
- 235000010627 Phaseolus vulgaris Nutrition 0.000 claims description 71
- 239000002253 acid Substances 0.000 claims description 60
- LHJPKLWGGMAUAN-UHFFFAOYSA-N 2-ethyl-2-methyl-butanoic acid Chemical compound CCC(C)(CC)C(O)=O LHJPKLWGGMAUAN-UHFFFAOYSA-N 0.000 claims description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- 229910001868 water Inorganic materials 0.000 claims description 25
- 238000004519 manufacturing process Methods 0.000 claims description 22
- 238000005406 washing Methods 0.000 claims description 19
- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical compound OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 claims description 18
- IAIWVQXQOWNYOU-BAQGIRSFSA-N [(z)-(5-nitrofuran-2-yl)methylideneamino]urea Chemical compound NC(=O)N\N=C/C1=CC=C([N+]([O-])=O)O1 IAIWVQXQOWNYOU-BAQGIRSFSA-N 0.000 claims description 18
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 17
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 17
- 235000013305 food Nutrition 0.000 claims description 11
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 claims description 10
- 235000010323 ascorbic acid Nutrition 0.000 claims description 8
- 239000011668 ascorbic acid Substances 0.000 claims description 8
- 229960005070 ascorbic acid Drugs 0.000 claims description 8
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 7
- 230000001954 sterilising effect Effects 0.000 claims description 7
- 235000019658 bitter taste Nutrition 0.000 claims description 6
- 238000000227 grinding Methods 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 3
- PPXUHEORWJQRHJ-UHFFFAOYSA-N ethyl isovalerate Chemical compound CCOC(=O)CC(C)C PPXUHEORWJQRHJ-UHFFFAOYSA-N 0.000 abstract 8
- 239000001813 ethyl (2R)-2-methylbutanoate Substances 0.000 abstract 4
- HCRBXQFHJMCTLF-UHFFFAOYSA-N ethyl 2-methylbutyrate Chemical compound CCOC(=O)C(C)CC HCRBXQFHJMCTLF-UHFFFAOYSA-N 0.000 abstract 4
- DKYWVDODHFEZIM-UHFFFAOYSA-N ketoprofen Chemical compound OC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-UHFFFAOYSA-N 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 45
- 235000012970 cakes Nutrition 0.000 description 32
- 239000008399 tap water Substances 0.000 description 30
- 235000020679 tap water Nutrition 0.000 description 30
- 241000239290 Araneae Species 0.000 description 16
- NTMYVTSWQJFCPA-UHFFFAOYSA-N (2-tert-butylpyrimidin-5-yl)oxy-ethoxy-propan-2-yloxy-sulfanylidene-$l^{5}-phosphane;[cyano-(4-fluoro-3-phenoxyphenyl)methyl] 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CCOP(=S)(OC(C)C)OC1=CN=C(C(C)(C)C)N=C1.CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 NTMYVTSWQJFCPA-UHFFFAOYSA-N 0.000 description 15
- 235000019219 chocolate Nutrition 0.000 description 14
- 230000020477 pH reduction Effects 0.000 description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 12
- 238000000576 coating method Methods 0.000 description 12
- 235000013861 fat-free Nutrition 0.000 description 12
- 239000000523 sample Substances 0.000 description 12
- 238000004458 analytical method Methods 0.000 description 11
- 238000001035 drying Methods 0.000 description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- 238000005520 cutting process Methods 0.000 description 10
- 238000004817 gas chromatography Methods 0.000 description 10
- 238000004949 mass spectrometry Methods 0.000 description 10
- 235000019221 dark chocolate Nutrition 0.000 description 9
- 238000011049 filling Methods 0.000 description 9
- 239000004615 ingredient Substances 0.000 description 9
- 239000004570 mortar (masonry) Substances 0.000 description 9
- 235000011007 phosphoric acid Nutrition 0.000 description 9
- 235000013618 yogurt Nutrition 0.000 description 9
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 8
- 239000004033 plastic Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 7
- 235000019197 fats Nutrition 0.000 description 7
- 239000013074 reference sample Substances 0.000 description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 6
- 239000003086 colorant Substances 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- -1 without limitation Substances 0.000 description 6
- PZNPLUBHRSSFHT-RRHRGVEJSA-N 1-hexadecanoyl-2-octadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[C@@H](COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCCCCCCCCCC PZNPLUBHRSSFHT-RRHRGVEJSA-N 0.000 description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 235000009508 confectionery Nutrition 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 235000021588 free fatty acids Nutrition 0.000 description 5
- 239000011630 iodine Substances 0.000 description 5
- 229910052740 iodine Inorganic materials 0.000 description 5
- 229910052700 potassium Inorganic materials 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000008347 soybean phospholipid Substances 0.000 description 5
- 238000004659 sterilization and disinfection Methods 0.000 description 5
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 235000011054 acetic acid Nutrition 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 235000013361 beverage Nutrition 0.000 description 4
- 235000014121 butter Nutrition 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 235000015165 citric acid Nutrition 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000004310 lactic acid Substances 0.000 description 4
- 235000014655 lactic acid Nutrition 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Substances [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 3
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 3
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 3
- 235000016623 Fragaria vesca Nutrition 0.000 description 3
- 240000009088 Fragaria x ananassa Species 0.000 description 3
- 235000011363 Fragaria x ananassa Nutrition 0.000 description 3
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 3
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 3
- 235000011034 Rubus glaucus Nutrition 0.000 description 3
- 244000235659 Rubus idaeus Species 0.000 description 3
- 235000009122 Rubus idaeus Nutrition 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 239000005862 Whey Substances 0.000 description 3
- 102000007544 Whey Proteins Human genes 0.000 description 3
- 108010046377 Whey Proteins Proteins 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000000174 gluconic acid Substances 0.000 description 3
- 235000012208 gluconic acid Nutrition 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 239000008101 lactose Substances 0.000 description 3
- 239000000787 lecithin Substances 0.000 description 3
- 229940067606 lecithin Drugs 0.000 description 3
- 235000010445 lecithin Nutrition 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 description 2
- VYLQGYLYRQKMFU-UHFFFAOYSA-N Ochratoxin A Natural products CC1Cc2c(Cl)cc(CNC(Cc3ccccc3)C(=O)O)cc2C(=O)O1 VYLQGYLYRQKMFU-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 244000290333 Vanilla fragrans Species 0.000 description 2
- 235000009499 Vanilla fragrans Nutrition 0.000 description 2
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- 239000000908 ammonium hydroxide Substances 0.000 description 2
- 235000013351 cheese Nutrition 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000008120 corn starch Substances 0.000 description 2
- 229940099112 cornstarch Drugs 0.000 description 2
- 235000021463 dry cake Nutrition 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 2
- 229940093915 gynecological organic acid Drugs 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
- 239000000347 magnesium hydroxide Substances 0.000 description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- RWQKHEORZBHNRI-BMIGLBTASA-N ochratoxin A Chemical compound C([C@H](NC(=O)C1=CC(Cl)=C2C[C@H](OC(=O)C2=C1O)C)C(O)=O)C1=CC=CC=C1 RWQKHEORZBHNRI-BMIGLBTASA-N 0.000 description 2
- DAEYIVCTQUFNTM-UHFFFAOYSA-N ochratoxin B Natural products OC1=C2C(=O)OC(C)CC2=CC=C1C(=O)NC(C(O)=O)CC1=CC=CC=C1 DAEYIVCTQUFNTM-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 229940072033 potash Drugs 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 235000015320 potassium carbonate Nutrition 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000005070 sampling Methods 0.000 description 2
- 235000020183 skimmed milk Nutrition 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Substances [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- 235000012141 vanillin Nutrition 0.000 description 2
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 2
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- 241000195940 Bryophyta Species 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 241001137251 Corvidae Species 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 241001489212 Tuber Species 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000003113 alkalizing effect Effects 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000021544 chips of chocolate Nutrition 0.000 description 1
- 235000019877 cocoa butter equivalent Nutrition 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 235000014510 cooky Nutrition 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 235000014103 egg white Nutrition 0.000 description 1
- 210000000969 egg white Anatomy 0.000 description 1
- 210000002969 egg yolk Anatomy 0.000 description 1
- 235000013345 egg yolk Nutrition 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000001459 mortal effect Effects 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- 229930183344 ochratoxin Natural products 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 235000015108 pies Nutrition 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 235000011962 puddings Nutrition 0.000 description 1
- 150000003216 pyrazines Chemical class 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 235000013570 smoothie Nutrition 0.000 description 1
- 235000019980 sodium acid phosphate Nutrition 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 235000021055 solid food Nutrition 0.000 description 1
- 235000013322 soy milk Nutrition 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229940005741 sunflower lecithin Drugs 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 235000008939 whole milk Nutrition 0.000 description 1
- 235000019220 whole milk chocolate Nutrition 0.000 description 1
- 235000008924 yoghurt drink Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/0003—Processes of manufacture not relating to composition or compounding ingredients
- A23G1/002—Processes for preparing or treating cocoa beans or nibs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/32—Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/50—Cocoa products, e.g. chocolate; Substitutes therefor characterised by shape, structure or physical form, e.g. products with an inedible support
- A23G1/52—Aerated, foamed, cellular or porous products, e.g. gas expanded
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/30—Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/56—Cocoa products, e.g. chocolate; Substitutes therefor making liquid products, e.g. for making chocolate milk drinks and the products for their preparation, pastes for spreading, milk crumb
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/36—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof characterised by the composition containing organic or inorganic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G9/00—Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor
- A23G9/32—Frozen sweets, e.g. ice confectionery, ice-cream; Mixtures therefor characterised by the composition containing organic or inorganic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/20—Synthetic spices, flavouring agents or condiments
- A23L27/202—Aliphatic compounds
- A23L27/2024—Aliphatic compounds having oxygen as the only hetero atom
- A23L27/2028—Carboxy compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/20—Synthetic spices, flavouring agents or condiments
- A23L27/205—Heterocyclic compounds
- A23L27/2052—Heterocyclic compounds having oxygen or sulfur as the only hetero atoms
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Abstract
Discloses a cocoa product selected from the group consisting of a cocoa powder, a cocoa liquor, and a cocoa butter, the cocoa product having a fruity flavour comprising: an increased amount of a fruity aroma compounds, wherein the fruity aroma compounds are selected from the group consisting of furaneol, phenylacetaldehyde, ethyl-2-methylpropanoate, ethyl-2-methylbutanoate, ethyl-3-methylbutanoate, and combinations of any thereof; wherein the cocoa product comprises an amount of fruity aroma compounds selected from the group consisting of at least 5 ?g/kg of ethyl-2-methylpropanoate, at least 15 ?g/kg of ethyl-2-methylbutanoate, at least 20 ?g/kg of ethyl-3-methylbutanoate, at least 50 ?g/kg of phenylacetaldehyde, at least 100 ?g/kg of furaneol, and combinations of any thereof. aneol, phenylacetaldehyde, ethyl-2-methylpropanoate, ethyl-2-methylbutanoate, ethyl-3-methylbutanoate, and combinations of any thereof; wherein the cocoa product comprises an amount of fruity aroma compounds selected from the group consisting of at least 5 ?g/kg of ethyl-2-methylpropanoate, at least 15 ?g/kg of ethyl-2-methylbutanoate, at least 20 ?g/kg of ethyl-3-methylbutanoate, at least 50 ?g/kg of phenylacetaldehyde, at least 100 ?g/kg of furaneol, and combinations of any thereof.
Description
TITLE
FRUITY FLAVORED COCOA PRODUCTS AND PROCESSES FOR
PRODUCING SUCH COCOA PRODUCTS
INVENTOR
Harrold Glenn Anijs
TECHNICAL FIELD
Methods for producing cocoa products with fruity flavors are
disclosed. Cocoa products including, without limitation, cocoa powders and cocoa
liquors produced according to such methods are also disclosed, as well as food
products including such cocoa products.
BACKGROUND ART
Cocoa bean processing includes fermenting harvested beans, drying
the beans, de-hulling the beans to produce nibs, sterilizing the nibs, roasting the nibs,
crushing the nibs into cocoa liquor, and optionally pressing the cocoa liquor to obtain
cocoa butter and cocoa powder. Variations in this process also are known. Dutched
cocoa powder is produced by alkalizing the nibs prior to roasting. Alkalization is a
process where nibs are heated in water in the presence of sodium, potassium,
ammonium, or magnesium hydroxide or carbonate, for example and without
limitation, potash (K CO ). The alkalization process alters the flavor, coloring, and
solubility of the cocoa powder in water.
Current commercial demands require a cocoa manufacturer to
produce cocoa products in a broad palette of colors, flavors, or both. While each
manufacturer understands that manipulation of processing conditions such as
temperature, water content, duration of processing time, and pH will affect the color
and flavor of the cocoa powder produced, there is no general consensus as to how to
produce a cocoa product of a consistently desirable color, flavor, or both.
US Patent Application Publication US 2008/0107783 describes
methods of producing bright red, brown, and red-brown cocoa products. Such
publication discloses novel colored cocoa products and uses thereof.
International Publication describes a process for
producing acidified red cocoa products and ingredients. Such methods are
performed on under-fermented or unfermented cocoa beans that are treated with an
acid, such as hydrochloric or phosphoric acid.
However, needs continually exist for processes for producing cocoa
products having desired colors, flavors or both. It is an object of the present
invention to go someway towards meeting this need and/or to provide the public
with a useful choice.
DISCLOSURE OF INVENTION
In one embodiment, a cocoa product having a fruity flavor comprises
an increased amount of a fruity aroma compounds.
[0008] In another embodiment, a method for producing a cocoa product
having a fruity flavor comprises mixing cocoa nibs, de-shelled cocoa beans, or a
combination thereof with an acid and water, and roasting the acidified nibs, the
acidified de-shelled cocoa beans, or the combination thereof.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] is a spider graph of flavor compounds present in various
embodiments of fruity cocoa products of the present invention.
is a spider graph showing the relative concentrations of six
flavor compounds of
is a spider graph of flavor compounds present in various
embodiments of fruity cocoa products of the present invention.
is a spider graph showing the relative concentrations of six
flavor compounds of
is a spider graph of flavor compounds present in various
embodiments of fruity cocoa products of the present invention.
[0014] is a spider graph showing the relative concentrations of six
flavor compounds of
is a spider graph of flavor compounds present in various
embodiments of fruity cocoa products of the present invention.
is a spider graph showing the relative concentrations of six
flavor compounds of
is a spider graph of flavor compounds present in various
embodiments of fruity cocoa products of the present invention.
[0018] is a spider graph of flavor compounds present in various
embodiments of fruity cocoa products of the present invention.
is a graph illustrating the amount of flavor compounds
present in various embodiments of fruity cocoa products of the present invention.
is a spider graph of flavor compounds present in various
embodiments of fruity cocoa products of the present invention.
is a graph illustrating a ratio of flavor compounds present in
various embodiments of fruity cocoa products of the present invention as compared
to a reference Arriba cocoa product.
is a spider graph of the ratio of flavor compounds depicted in
.
is a graph illustrating a ratio of flavor compounds present in
various embodiments of fruity cocoa products of the present invention as compared
to a reference natural cocoa product.
is a spider graph of the ratio of flavor compounds depicted in
.
is a graph illustrating a ratio of flavor compounds present in
various embodiments of fruity cocoa products of the present invention as compared
to a reference Arriba cocoa product.
MODES FOR CARRYING OUT THE INVENTION
[0026] In one embodiment, fruity flavored cocoa products are disclosed. The
fruity flavored cocoa products have a fresh, fruity flavor and taste. Specifically, in a
first aspect, the invention provides a cocoa product selected from the group
consisting of a cocoa powder, a cocoa liquor, and a cocoa butter, the cocoa product
having a fruity flavor comprising:
an increased amount of a fruity aroma compounds, wherein the fruity aroma
compounds are selected from the group consisting of furaneol, phenylacetaldehyde,
ethylmethylpropanoate, ethylmethylbutanoate, ethylmethylbutanoate, and
combinations of any thereof; wherein the cocoa product comprises an amount of
fruity aroma compounds selected from the group consisting of at least 5 µg/kg of
ethylmethylpropanoate, at least 15 µg/kg of ethylmethylbutanoate, at least 20
µg/kg of ethylmethylbutanoate, at least 50 µg/kg of phenylacetaldehyde, at least
100 µg/kg of furaneol, and combinations of any thereof.
In a second aspect, the invention provides a food product comprising
the cocoa product of the invention.
[0027a] In a third embodiment, a method for producing cocoa products
having a fruity flavor is disclosed. The method includes mixing cocoa nibs, de-
shelled beans, or a combination thereof with an acid and water, and roasting the
acidified cocoa nibs, de-shelled beans, or the combination thereof; wherein the cocoa
nibs, the de-shelled cocoa beans, or the combination thereof are good fermented. In
another embodiment, the acidified cocoa nibs, the acidified de-shelled, beans, or the
combination thereof is washed with water.
In a further embodiment, the acid is selected from the group
consisting of gluconic delta lactone acid, phosphoric acid, ascorbic acid, sodium
bisulphate, acid, and combinations of any thereof. The cocoa nibs, the de-shelled
beans, or the combination thereof may be good fermented, under fermented, or a
combination thereof.
In yet an additional embodiment, the nibs, the de-shelled beans, or
the combination thereof are sterilized.
[0030] In an additional embodiment, the nibs, the de-shelled beans, or the
combination thereof may be in contact with the acid for a period of from about 0.5 to
about 4 hours, at a temperature of between about 15°C to about 90°C, or a
combination of such time and temperature.
In another embodiment, the roast cocoa nibs, the roast de-shelled
beans, or the combination thereof are roasted to a moisture content of less than about
In yet a further embodiment, the roast cocoa nibs, the roast de-shelled
beans, or the combination thereof are ground, thus producing cocoa liquor. The
cocoa liquor may be separated into cocoa butter and cocoa presscake, or the cocoa
liquor may be defatted. The cocoa presscake may be further ground into cocoa
powder.
After such processing, the beans or nibs may be further roasted
and/or ground to cocoa liquor and, optionally, pressed into cocoa powder presscake
and cocoa butter. The presscake may be ground to produce cocoa powder. This
process yields cocoa products having fruity flavors and such cocoa products may be
unusually bright, and typically red, brown and red-brown.
In an additional embodiment, a cocoa product having an increased
amount of at least one fruity aroma compound is disclosed. The fruity aroma
compound is selected from the group consisting of furaneol, phenylacetaldehyde,
ethylmethylpropanoate, ethylmethylbutanoate, ethylmethylbutanoate, and
combinations of any thereof.
In a further embodiment, a cocoa product described herein comprises
an amount of a fruity aroma compound selected from the group consisting of at least
2.5 µg/kg of ethylmethylpropanoate, at least 5 µg/kg of ethyl
methylpropanoate, at least 7.5 µg/kg of ethylmethylbutanoate, at least 15 µg/kg
of ethylmethylbutanoate, at least 10 µg/kg of ethylmethylbutanoate, at least 20
µg/kg of ethylmethylbutanoate, at least 50 µg/kg of phenylacetaldehyde, at least
100 µg/kg of furaneol, and combinations of any thereof.
In another embodiment, the fruity flavored cocoa products described
herein are cocoa powder, cocoa liquor, cocoa butter, or combinations of any thereof.
In another embodiment, the cocoa products described herein are
desirable since the cocoa products have an increase in fruity flavors, yet have less
bitterness. The bitterness may be associated with compounds such as polyphenols,
pyrazines, non-volatile compounds, and combinations of any thereof. Thus, in
another embodiment, cocoa products produced from good fermented cocoa beans
having fruitier flavor and less bitterness as compared to cocoa products produced
from under fermented or unfermented cocoa beans are disclosed. In another
embodiment, the cocoa products of the present invention have less than 500 µg/kg of
acrylamide, or less than 250 µg/kg of acrylamide.
Fruity flavored cocoa products are desired in certain food
applications. For instance, fruity cocoa products may fit well with yoghurt flavored
food products or other food flavors. In one embodiment, the cocoa products
described herein have an increased amount of fruity aroma compounds or fruity
compounds as compared to conventional cocoa products. Fruity aroma compounds
include, but are not limited to, furaneol, phenylacetaldehyde, ethyl
methylpropanoate, ethylmethylbutanoate, ethylmethylbutanoate, and
combinations of any thereof.
In another embodiment, the fruity flavored cocoa products described
herein may have a bright color which refers to cocoa products with a C value more
than about 18.0, 19.0, 20.0, 21.0, 22.0, 23.0, 24.0, 25.0, or higher, inclusive of intervals
between those values. In another embodiment, the fruity flavored cocoa products
described herein are red, redder, or more red which refers to a cocoa product having
an H value approximately in the range of from about 35 to about 55, about 40 to
about 45, or about 48 to about 56, (CIE 1976) that has an H value less than another,
reference cocoa powder. In another embodiment, the fruity flavored cocoa products
of the present invention are brown, browner, or more brown and refer to a cocoa
product with an H value approximately in the range of from about 45 to about 55
(CIE 1976) that has an H value greater than another, reference cocoa powder.
In yet an additional embodiment, a fruity flavored cocoa product
described herein has a color value selected from the group consisting of an L value of
between about 18 to about 29, an L value of between about 22 to about 29, a C value
of about 23 to about 30, an H value of between about 35 to about 55, and
combinations of any thereof. Further, the fruity flavored cocoa product described
herein may have a pH of between about 3 to about 6, a pH of between about 4.5 to
about 6, or a pH of between about 4.5 to 5.
[0041] In one embodiment, a starting material for the processes described
herein may be de-shelled cocoa beans which refers to any suitable cocoa bean
fraction/product having the shells substantially removed, broken, and/or
winnowed. Non-limiting examples of de-shelled cocoa beans include, but are not
limited to, nibs, kernels, and cotyledons. De-shelled cocoa beans typically contain a
small fraction of contaminating shells that are within commercially acceptable
tolerances since no de-shelling process is 100% complete.
In another embodiment, a pH of the de-shelled cocoa beans may be
manipulated by placing an acidic or alkaline agent in contact with the de-shelled
cocoa beans. Optionally, after the acidic or alkaline agent is placed in contact with the
de-shelled cocoa beans, the de-shelled cocoa beans may be washed. Alkalization
agents are known in the art, and may include, but are not limited to, water and
sodium, potassium, ammonium or magnesium hydroxide or carbonate, potash
(K CO ), and combinations of any thereof. Acid agents are known in the art and may
include, without limitation food grade acids or organic acids. Examples of food grade
acids include, but are not limited to, hydrochloric acid, sodium acid sulfate, sodium
bisulphate acid, sodium acid phosphate, phosphoric acid, and combinations of any
thereof. Examples of organic acids include, but are not limited to, gluconic acid,
gluconic delta lactone acid, ascorbic acid, citric acid, lactic acid, lemon juice, lime
juice, acetic acid, fumaric acid, adipic acid, malic acid, tartaric acid, and combinations
of any thereof.
In an additional embodiment, the cocoa beans used to produce the
fruity flavored cocoa products described herein are good fermented. In a further
embodiment, the cocoa beans used to produce the fruity flavored cocoa products
described herein are under- or un- fermented.
In a further embodiment, another process parameter that may help
achieve optimal coloring of the fruity flavored cocoa product is to minimize
sterilization of the beans or nibs prior to pH manipulation.
In one embodiment, the fruity flavored cocoa products produced
herein are suitable for many commercial purposes, including, without limitation,
food products. Examples of food products include, but are not limited to, chocolate,
dark chocolate, milk chocolate, semi-sweet-chocolate, baking chocolate, candies,
pralines, truffles, candy bars, flavoring syrup, confectionary coatings, compound
coatings, fillings, beverages, milk, ice cream, beverage mixes, smoothies, soy milk,
cakes, cheesecakes, cookies, pies, diet bars, meal-substitute solid foods and
beverages, energy bars, chocolate chips, yogurt, yogurt drinks, pudding, mousse,
mole, chocolates with lower bitterness, chocolate with fillings such as yogurt,
cheesecake or fruit, and cocoa powders for use in cheese, dairy or beverages.
In another embodiment, fruity flavored cocoa products including,
without limitation, powders and/or liquors having extraordinary brightness are
produced by the methods described herein. The fruity flavored cocoa products may
have an L color co-ordinate value greater than 16 or in a range of 22-29, a pH less
than 7.0 or in a range of 3.0-6.0, and exhibit a high brightness expressed by a C color
coordinate value greater than 20 or in a range of 23-30. H-values (CIE 1976) may fall
in the red-to-brown range of between 35-55.
A number of objective methods for measuring the color of cocoa
products are known. In one method, the Hunter color system or CIE 1976 (CIELAB)
and like systems, color may be described in terms of three parameters: Lightness (L)--
the light or dark aspect of a color, where the lower the L-value, the darker the cocoa
powder will appear; Chroma (C)--the intensity of a color by which one distinguishes
a bright or gray color, where the higher the C-value, the brighter the powder will be;
and Hue (H)-- referring to color in daily speech, such as red, yellow, or blue. For
cocoa powders, a low H value indicates a red color and a high H-value indicates a
brown color.
The CIE 1976 color system describes colors in terms of coordinates L,
"a*" and "b*". The L coordinate is consistent with the Value of Lightness, and from
the a* and b* coordinates, the Chroma and Hue can be calculated as follows: C*=
{square root over (a* +b* )}; H=arctan(b*/a*).
[0049] The spectral color is the result of the source of light and the reflecting
surface. For a good reproducible measurement of color, the source of light is
standardized. There are two basic approaches for measuring color: visually or by
instrumentation. There is a natural human tendency to trust only "one's own eyes."
For this reason, colors are still frequently judged visually. To be able to do this in a
reproducible manner, certain standard conditions should be met: the light source, for
example and without limitation, a CIE standard light source; the positions of the
sample, relative to the light source, which are preferably at an angle of 45° to each
other; the background of the sample, uniform and preferably gray; the distance
between the eyes and the sample and position of the eyes relative to the sample; and
the size of the sample.
In practice, color cabinets are used with standard light sources for
visual color determinations. Color meters and spectrophotometers are used for
instrument color readings. Instrument color measurements were made in the
Examples herein using a Datacolor Spectraflash 500 Color spectrophotometer in the
manner described herein. Unless otherwise indicated, the color values described in
the Examples, and all reference herein to color values L, C, H, a and b (a* and b*,
respectively), are readings using the Datacolor Spectraflash 500 Color
spectrophotometer. The color parameters described herein refer to the L, C, H
parameters that can be calculated from L, a and b readings according to the CIE 1976
system. The color values recited herein are approximate in the sense that color
measurements may vary from spectrophotometer-to-spectrophotometer, typically in
the range of +/- 0.5 for L, C and H values. Therefore, the stated values for L, C and H
are intended to include such variation inherent between spectrophotometers. The
color values of cocoa powders, unless indicated otherwise, are obtained on samples
of pulverized cocoa cakes (post pressing to remove cocoa butter) in water.
[0050a] The term “comprising” as used in this specification and claims means
“consisting at least in part of”. When interpreting statements in this specification,
and claims which include the term “comprising”, it is to be understood that other
features that are additional to the features prefaced by this term in each statement or
claim may also be present. Related terms such as “comprise” and “comprised” are to
be interpreted in similar manner.
The following examples illustrate various non-limiting embodiments
of the compositions within the present disclosure and are not restrictive of the
invention as otherwise described or claimed herein.
EXAMPLES
Example 1. Production of cocoa products with ascorbic acid.
Under fermented Sulawesi beans were used to produce 2,000 grams
of under-fermented nibs. The nibs were mixed with 3,000 mL of a 0.5M ascorbic acid
solution having a temperature of 25°C in a plastic bucket having a volume of eight
liters. After stirring, the nibs in the acid solution were placed in a stove with rotating
air at a temperature of 25°C for four hours.
The wet, acidified nibs were drained to remove the excess acid
solution. The drained nibs were rinsed several times with tap water until the pH of
the watery residue coming off of the rinsed nibs was in the range of 3.2-5.0. After
rinsing, the moisture content of the nibs was in the range of 44-50%.
The washed nibs were dried in a stove with rotating air at a
temperature of 50°C for 20 hours to reduce the moisture content to the range of 3-5%.
The dried nibs were roasted in a Retch fluidized bed dryer (i.e., jet roaster) for 15
minutes at a temperature of 110°C to lower the moisture to 1-2%.
The roasted nibs were ground to coarse liquor in a household coffee
mill, and further ground to cocoa liquor of a desired fineness in a Retsch laboratory
mortar mill.
A first portion of the fine ground liquor was extracted to obtain a fat
free cocoa powder and a second portion of the fine ground liquor was hydraulic
pressed into small cakes and filtered cocoa butter. The cakes were broken into small
pieces and the pieces were pulverized into cocoa powder with a Retsch cutting mill
with sieves having holes of 0.5 mm.
Example 2. Production of cocoa products with ascorbic acid.
Under fermented Sulawesi beans were used to produce 2,000 grams
of under-fermented nibs. The nibs were mixed with 3,000 mL of a 0.5M ascorbic acid
solution having a temperature of 25°C in a plastic bucket having a volume of eight
liters. After stirring, the nibs in the acid solution were placed in a stove with rotating
air at a temperature of 25°C for four hours.
The wet, acidified nibs were drained to remove the excess acid
solution. The drained nibs were rinsed several times with tap water until the pH of
the watery residue coming off of the rinsed nibs was in the range of 3.2-5.0. After
rinsing, the moisture content of the nibs was in the range of 44-50%.
The washed nibs were dried in a Retch fluidized bed dryer (i.e., jet
roaster) for 75 minutes at a temperature of 120°C to reduce the moisture content to 1-
The roasted nibs were ground to coarse liquor in a household coffee
mill, and further ground to cocoa liquor of a desired fineness in a Retsch laboratory
mortar mill.
A first portion of the fine ground liquor was extracted to obtain a fat
free cocoa powder and a second portion of the fine ground liquor was hydraulic
pressed into small cakes and filtered cocoa butter. The cakes were broken into small
pieces and the pieces were pulverized into cocoa powder with a Retsch cutting mill
with sieves having holes of 0.5 mm.
Example 3. Production of cocoa products with gluconic delta lactone
acid solution.
Under fermented Sulawesi beans were used to produce 2,000 grams
of under-fermented nibs. The nibs were mixed with 3,000 mL of a 0.5 M gluconic
delta lactone acid solution having a temperature of 25°C were mixed in a plastic
bucket having a volume of eight liters. After stirring, the nibs in the acid solution
were placed in a stove with rotating air at a temperature of 25°C for four hours.
The wet, acidified nibs were drained to remove the excess acid
solution. The drained nibs were rinsed several times with tap water until the pH of
the watery residue coming off of the rinsed nibs was in the range of 3.2-5.0. After
rinsing, the moisture content of the nibs was in the range of 44-50%.
[0067] The washed nibs were dried in a stove with rotating air at a
temperature of 50°C for 20 hours to reduce the moisture content to the range of 3-5%.
The dried nibs were roasted in a Retch fluidized bed dryer (i.e., jet roaster) for 15
minutes at a temperature of 110°C to lower the moisture to 1-2%.
The roasted nibs were ground to coarse liquor in a household coffee
mill, and further ground to cocoa liquor of a desired fineness in a Retsch laboratory
mortar mill.
A first portion of the fine ground liquor was extracted to obtain a fat
free cocoa powder and a second portion of the fine ground liquor was hydraulic
pressed into small cakes and filtered cocoa butter. The cakes were broken into small
pieces and the pieces were pulverized into cocoa powder with a Retsch cutting mill
with sieves having holes of 0.5 mm.
Example 4. Production of cocoa products with gluconic delta lactone
acid solution.
Under fermented Sulawesi beans were used to produce 2,000 grams
of under-fermented nibs. The nibs were mixed with 3,000 mL of a 0.5 M gluconic
delta lactone acid solution having a temperature of 25°C were mixed in a plastic
bucket having a volume of eight liters. After stirring, the nibs in the acid solution
were placed in a stove with rotating air at a temperature of 25°C for four hours.
The wet, acidified nibs were drained to remove the excess acid
solution. The drained nibs were rinsed several times with tap water until the pH of
the watery residue coming off of the rinsed nibs was in the range of 3.2-5.0. After
rinsing, the moisture content of the nibs was in the range of 44-50%.
[0073] The washed nibs were dried in a Retch fluidized bed dryer (i.e., jet
roaster) for 75 minutes at a temperature of 120°C to reduce the moisture content to 1-
The roasted nibs were ground to coarse liquor in a household coffee
mill, and further ground to cocoa liquor of a desired fineness in a Retsch laboratory
mortar mill.
A first portion of the fine ground liquor was extracted to obtain a fat
free cocoa powder and a second portion of the fine ground liquor was hydraulic
pressed into small cakes and filtered cocoa butter. The cakes were broken into small
pieces and the pieces were pulverized into cocoa powder with a Retsch cutting mill
with sieves having holes of 0.5 mm.
Example 5. Production of cocoa products with sodium bisulphate acid
solution.
Under fermented Sulawesi beans were used to produce 2,000 grams
of under-fermented nibs. The nibs were mixed with 3,000 mL of a 0.5 M sodium
bisulphate acid solution having a temperature of 25°C were mixed in a plastic bucket
having a volume of eight liters. After stirring, the nibs in the acid solution were
placed in a stove with rotating air at a temperature of 25°C for four hours.
The wet, acidified nibs were drained to remove the excess acid
solution. The drained nibs were rinsed several times with tap water until the pH of
the watery residue coming off of the rinsed nibs was in the range of 3.2-5.0. After
rinsing, the moisture content of the nibs was in the range of 44-50%.
The washed nibs were dried in a stove with rotating air at a
temperature of 50°C for 20 hours to reduce the moisture content to the range of 3-5%.
The dried nibs were roasted in a Retch fluidized bed dryer (i.e., jet roaster) for 15
minutes at a temperature of 110°C to lower the moisture to 1-2%.
The roasted nibs were ground to coarse liquor in a household coffee
mill, and further ground to cocoa liquor of a desired fineness in a Retsch laboratory
mortar mill.
A first portion of the fine ground liquor was extracted to obtain a fat
free cocoa powder and a second portion of the fine ground liquor was hydraulic
pressed into small cakes and filtered cocoa butter. The cakes were broken into small
pieces and the pieces were pulverized into cocoa powder with a Retsch cutting mill
with sieves having holes of 0.5 mm.
Example 6. Production of cocoa products with sodium bisulphate acid
solution.
Under fermented Sulawesi beans were used to produce 2,000 grams
of under-fermented nibs. The nibs were mixed with 3,000 mL of a 0.5 M sodium
bisulphate acid solution having a temperature of 25°C were mixed in a plastic bucket
having a volume of eight liters. After stirring, the nibs in the acid solution were
placed in a stove with rotating air at a temperature of 25°C for four hours.
The wet, acidified nibs were drained to remove the excess acid
solution. The drained nibs were rinsed several times with tap water until the pH of
the watery residue coming off of the rinsed nibs was in the range of 3.2-5.0. After
rinsing, the moisture content of the nibs was in the range of 44-50%.
The washed nibs were dried in a Retch fluidized bed dryer (i.e., jet
roaster) for 75 minutes at a temperature of 120°C to reduce the moisture content to 1-
[0086] The roasted nibs were ground to coarse liquor in a household coffee
mill, and further ground to cocoa liquor of a desired fineness in a Retsch laboratory
mortar mill.
A first portion of the fine ground liquor was extracted to obtain a fat
free cocoa powder and a second portion of the fine ground liquor was hydraulic
pressed into small cakes and filtered cocoa butter. The cakes were broken into small
pieces and the pieces were pulverized into cocoa powder with a Retsch cutting mill
with sieves having holes of 0.5 mm.
Example 7. Production of cocoa products with phosphoric acid.
[0089] Under fermented Sulawesi beans were used to produce 2,000 grams
of under-fermented nibs. The nibs were mixed with 3,000 mL of a 0.16 M phosphoric
acid solution having a temperature of 25°C were mixed in a plastic bucket having a
volume of eight liters. After stirring, the nibs in the acid solution were placed in a
stove with rotating air at a temperature of 25°C for four hours.
[0090] The wet, acidified nibs were drained to remove the excess acid
solution. The drained nibs were rinsed several times with tap water until the pH of
the watery residue coming off of the rinsed nibs was in the range of 3.2-5.0. After
rinsing, the moisture content of the nibs was in the range of 44-50%.
The washed nibs were dried in a stove with rotating air at a
temperature of 50°C for 20 hours to reduce the moisture content to the range of 3-5%.
The dried nibs were roasted in a Retch fluidized bed dryer (i.e., jet roaster) for 15
minutes at a temperature of 110°C to lower the moisture to 1-2%.
The roasted nibs were ground to coarse liquor in a household coffee
mill, and further ground to cocoa liquor of a desired fineness in a Retsch laboratory
mortar mill.
A first portion of the fine ground liquor was extracted to obtain a fat
free cocoa powder and a second portion of the fine ground liquor was hydraulic
pressed into small cakes and filtered cocoa butter. The cakes were broken into small
pieces and the pieces were pulverized into cocoa powder with a Retsch cutting mill
with sieves having holes of 0.5 mm.
Example 8. Production of cocoa products with phosphoric acid.
Under fermented Sulawesi beans were used to produce 2,000 grams
of under-fermented nibs. The nibs were mixed with 3,000 mL of a 0.16 M phosphoric
acid solution having a temperature of 25°C were mixed in a plastic bucket having a
volume of eight liters. After stirring, the nibs in the acid solution were placed in a
stove with rotating air at a temperature of 25°C for four hours.
The wet, acidified nibs were drained to remove the excess acid
solution. The drained nibs were rinsed several times with tap water until the pH of
the watery residue coming off of the rinsed nibs was in the range of 3.2-5.0. After
rinsing, the moisture content of the nibs was in the range of 44-50%.
The washed nibs were dried in a Retch fluidized bed dryer (i.e., jet
roaster) for 75 minutes at a temperature of 120°C to reduce the moisture content to 1-
[0098] The roasted nibs were ground to coarse liquor in a household coffee
mill, and further ground to cocoa liquor of a desired fineness in a Retsch laboratory
mortar mill.
A first portion of the fine ground liquor was extracted to obtain a fat
free cocoa powder and a second portion of the fine ground liquor was hydraulic
pressed into small cakes and filtered cocoa butter. The cakes were broken into small
pieces and the pieces were pulverized into cocoa powder with a Retsch cutting mill
with sieves having holes of 0.5 mm.
Example 9. Production of reference or control cocoa product.
Under fermented Sulawesi beans were used to produce 2,000 grams
of under-fermented nibs. These nibs were not placed in contact with an acid solution
as described in Examples 1-8.
The nibs were dried in a Retch fluidized bed dryer (i.e., jet roaster) for
75 minutes at a temperature of 120°C to reduce the moisture content to 1-2%.
The roasted nibs were ground to coarse liquor in a household coffee
mill, and further ground to cocoa liquor of a desired fineness in a Retsch laboratory
mortar mill.
A first portion of the fine ground liquor was extracted to obtain a fat
free cocoa powder and a second portion of the fine ground liquor was hydraulic
pressed into small cakes and filtered cocoa butter. The cakes were broken into small
pieces and the pieces were pulverized into cocoa powder with a Retsch cutting mill
with sieves having holes of 0.5 mm.
Tables 1A and 1B show the process conditions used to produce the
cocoa products of Examples 1-9.
[00106] Table 1A. Process conditions of cocoa products of Examples 1-4 and
the control or reference, Example 9.
Example number Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. 9
nibs from 100% Bad fermented
Sulawesi beans
Charge Weight (g) 2000 2000 2000 2000 2000
moisture content (%) 6.4 6.4 6.4 6.4 6.4
Fat content (%) 50.5 50.5 50.5 50.5 50.5
Butter of Sulawesi nib
Free Fatty Acid content (%) 1.1 1.1 1.1 1.1 1.1
Iodine value 36.2 36.2 36.2 36.2 36.2
Acidification with acid solution during
4 hrs
3000 g of acid solution ( 25 C ) Ascorbic Ascorbic GDL GDL
Acid solution (w%) 8.1 8.1 8.2 8.2
Molarity (M) of acid solution 0.5 0.5 0.5 0.5
( mol / liter)
Specific weight ( gram/liter) 1039.3 1039.3 1051.1 1051.1
pH 2.22 2.22 2.01 2.01
Charges of tap water for washing the nib
Tap water for every washing step 3000 3000 3000 3000
of the nibs ( g)
Temperature tap water ( C ) 21.6 21.6 20 20
pH of the tap water 6.32 6.32 6.32 6.32
pH of the Watery residue
after 4 hours acidification 3.72 3.72 3.37 3.37
after first washing with tapwater 3.88 3.88 3.55 3.55
after second washing with tap water 3.97 3.97 3.66 3.66
after third washing with tap water 4.07 4.07 3.75 3.75
Drying methods of the wet acidified nibs Stove Jet roast Stove Jet roast Jet roast
Moisture content of the nib (%) :
Raw unacidified nibs (w%) 6.4 6.4 6.4 6.4 6.4
After washings with water 46.6 46.6 44.9 44.9 13.5
After 20 hrs drying at 50 C in the stove 4.26 4,9
After 75 min Jet roasting at 120 C 1.8 1.9
(SP is 120 C)
After 25 min jet roasting at 100 C < 1 < 1 < 1 < 1 < 1
(before grinding)
Table 1B. Process conditions of cocoa products of Examples 5-8 and
the control, Example 9.
Example number Ex. 5 Ex. 6 Ex. 7 Ex. 8 Ex. 9
nibs from 100% sulawesi beans
(bad fermented)
Charge Weight (g) 2000 2000 2000 2000 2000
moisture content (%) 6.4 6.4 6.4 6.4 6.4
Fat content (%) 50.5 50.5 50.5 50.5 50.5
Butter of raw nib
Free Fatty Acid content (%) 1.1 1.1 1.1 1.1
Iodine value 36.2 36.2 36.2 36.2
Acidification with acid solution during
4 hrs
3000 g of acid solution ( 25 C ) NaHSO4 NaHSO4 H3PO4 H3PO4
Acid solution (w%) 5.7 5.7 1.6 1.6
Molarity (M) of acid solution ( mol /
0.51 0.51 0.16 0.16
liter)
Specific weight ( gram/liter) 1042.5 1042.5 1026.4 1026.4
pH 0.86 0.86 1.45 1.45
Charges of tap water for washing the nib
Tap water for every washing step of the
3000 3000 3000 3000
nibs ( g)
Temperature tap water ( C ) 21.6 21.6 21.6 21.6
pH of the tap water 6.32 6.32 6.32 6.32
pH of the Watery residue
after 4 hours acidification 1.63 1.63 3.64 3.64
after first washing with tap water 2.12 2.12 4.09 4.09
after second washing with tap water 2.32 2.32 4.58 4.58
after third washing with tap water 2.52 2.52 4.99 4.99
after fourth washing with tap water 2.68 2.68 5.06 5.06
after five washing with tap water 2.82 2.82
after six washing with tap water 2.96 2.96
after seven washing with tap water 3.21 3.21
after eight washing with tap water 3.45 3.45
after Nine washings with tap water 3.72 3.72
Drying methods of the wet acidified nibs Jet Roast Stove Jet roast Stove Jet roast
Moisture content of the nib (%) :
Raw un acidified nibs (w%) 6.4 6.4 6.4 6.4 6.4
After washings with water 47.6 47.6 43.5 43.5 13.5
After 20 hrs drying at 50 C in the stove 4.2 4.3
After 75 min Jet roasting at 120 C
2.5 2.5
(SP is 120 C)
After 25 min jet roasting at 100 C
< 1 < 1 < 1 < 1 < 1
(before grinding)
The cocoa liquor, cocoa powder and cocoa butter produced in
Examples 1-9 were characterized as shown in Table 2.
Table 2. Color of cocoa liquor and cocoa powder of Examples 1-9.
Example number 1 2 3 4 5 6 7 8 9
Acid Ascorbic Ascorbic GDL GDL NaHSO NaHSO H PO H PO
4 4 3 4 3 4
Drying in stove X X X X
Drying in jet
X X X X
roaster
Liquor
Intrinsic Colour
FFD ( in water)
L ffd 27.58 25.44 25.51 23.65 23.18 25.58 23.30 24.28 23.26
C ffd 27.00 25.73 23.77 23.98 27.26 27.32 23.54 24.17 23.85
H ffd 52.14 50.09 48.32 48.53 42.25 39.44 49.02 50.67 53.31
a ffd 16.57 16.51 15.80 15.88 20.18 21.09 15.44 15.31 14.25
b ffd 21.32 19.74 17.75 17.97 18.33 17.35 17.77 18.69 19.12
Powder
pH 4.52 4.53 4.38 4.48 3.4 3.47 4.76 4.72 5.96
% moisture 2.37 2.56 2.35 2.26 2.41 2.55 2.31 2.83 2.07
% fat 15.67 13.88 14.92 12.98 13.78 13.93 13.56 16.68 15.11
Intrinsic Colour
(in water)
L tot 30.13 27.67 27.87 25.64 25.26 27.78 25.37 26.94 25.53
C tot 27.89 26.56 24,55 24.75 28.12 28.05 24.34 25.17 24.80
H tot 52.74 50.57 48.80 48.91 42.57 39.76 49.42 51.22 53.74
a tot 16.88 16.87 16.17 16.27 20.71 21.57 15.84 15.77 14.67
b tot 22.2 20.52 18.47 18.65 19.02 17.94 18.49 19.62 20.00
filtered Butter
Free fatty acid
1.02 1.00 1.00 0.99 1.08 1.03 1.00 0.94 1.06
(VVZ)
Iodine value(I.V.) 36.2 36.3 36.2 36.2 36.2 36.2 36.3 36.3 36.1
Table 2 indicates that the strength of the acid solution and the drying
method has an influence on the color and on the pH of the cocoa product produced.
Also, drying in the jet roaster appears to make the final color darker and redder. The
stronger acid solution also makes the color of the powders brighter and redder.
[00111] The color values L, C, and H were determined for the cocoa products
of Examples 1-9 using the CIE LAB data color system. Such colors were also
transformed into the color values L, a, and B of the Hunter Lab color system. These
colors are shown in Table 3.
Table 3. Color values of cocoa products of Examples 1-8 and the
control, Example 9.
Example Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 Ex. 7 Ex. 8 Ex. 9
pH 4.52 4.53 4.38 4.48 3.4 3.47 4.76 4.72 5.96
CIE lab
L tot 30.13 27.67 27.87 25.64 25.26 27.78 25.37 26.94 25.53
C tot 27.89 26.56 24.55 24.75 28.12 28.05 24.34 25.17 24.80
H tot 52.74 50.57 48.80 48.91 42.57 39.76 49.42 51.22 53.74
a tot 16.88 16.87 16.17 16.27 20.71 21.57 15.84 15.77 14.67
b tot 22.2 20.52 18.47 18.65 19.02 17.94 18.49 19.62 20.00
Hunter lab
L tot 25.08 23.10 23.26 21.51 21.21 23.19 21.30 22.52 21.42
C tot 15.50 14.61 13.82 13.50 15.99 16.79 13.19 13.71 13.00
H tot 48.31 46.00 45.72 44.78 36.63 35.26 45.45 47.31 49.57
a tot 10.31 10.15 9.65 9.58 12.84 13.71 9.25 9.29 8.43
b tot 11.58 10.51 9.89 9.51 9.54 9.70 9.40 10.08 9.89
An analysis was done on the cocoa powders produced in Examples 1-
9. The results are shown in Tables 4A and 4B.
Table 4A. Lab analysis results on cocoa powders of Examples 1-4 and
the control, Example 9.
Example number Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. 9
Type drying process Jet roast Stove Stove Jet roast Jet roast
Potassium as K (%) 0.5 0.5 0.49 0.47 2.0
Sodium as Na (%) 0.0068 0.0079 0.0047 0.0048 0.027
Ash content (%) 2.92 2.98 2.82 2.92 6.36
Total alkalinity (ml/100g) 30.54 31.7 25.83 26.16 75.12
Total Iron as Fe (mg/kg) 41 42 48 46 59
Aluminium as Al (mg/kg) 31 29 22 20 51
Silicium as Si (%) <0.01 <0.01 <0.01 <0.01 0.02
Phosphorous as P (%) 0.54 0.55 0.61 0.35 0.89
Sulphate as SO4 (%) < 0.2 < 0.2 < 0.2 < 0.2 < 0.2
Ochratoxin A (ug/kg) < 0.4 < 0.4 < 0.4 < 0.4 < 0.4
Acrylamide (ug/kg) 100 160 170 190 830
Acetic acid (%) 0.05 0.06 0.06 0.06 0.26
Citric acid (%) 0.47 0.38 0.44 0.33 1.53
Lactic acid (%) 0.05 0.05 0.07 0.05 0.26
[00115] Table 4B. Lab analysis results on cocoa powders of Examples 5-8 and
the control, Example 9.
Example number Ex. 5 Ex. 6 Ex. 7 Ex. 8 Ex. 9
Type drying process Jet roast Stove Jet roast Stove Jet roast
Potassium as K (%) 0.15 0.18 0.59 0.54 2.0
Sodium as Na (%) 0.1 0.11 0.027 0.024 0.027
Ash content (%) 2.02 2.04 3.63 3.46 6.36
Total alkalinity (ml/100g) 13.78 12.46 24.71 26.58 75.12
Total Iron as Fe (mg/kg) 60 62 49 47 59
Aluminium as Al (mg/kg) 22 24 22 26 51
Silicium as Si (%) <0.01 <0.01 <0.01 <0.01 0.02
Phosphorous as P (%) 0.43 0.45 0.61 0.41 0.89
Sulphate as SO4 (%) < 0.2 < 0.2 < 0.2 < 0.2 < 0.2
Ochratoxin A (ug/kg) < 0.4 < 0.4 < 0.4 < 0.4 < 0.4
Acrylamide (ug/kg) 140 85 280 320 830
Acetic acid (%) 0.05 0.03 0.07 0.07 0.26
Citric acid (%) 0.11 0.22 0.4 0.45 1.53
Lactic acid (%) 0.02 0.02 0.06 0.06 0.26
shows a flavor profile of compounds present in the cocoa
liquors produced in Ex. 1, Ex. 2, and the control, Ex. 9. Gas chromatography and
mass spec was used to determine the amount of the compounds shown in The
graph in shows ratios of the concentrations of compounds present in the cocoa
liquors of Ex. 1, Ex. 2, and the control, Ex. 9.
shows a flavor profile of six compounds present in the cocoa
liquors produced in Ex. 1, Ex. 2, and the control, Ex. 9. Gas chromatography and
mass spec was used to determine the amount of the compounds shown in The
graph in shows ratios of the concentrations of compounds present in the cocoa
liquors of Ex. 1, Ex. 2, and the control, Ex. 9.
shows a flavor profile of compounds present in the cocoa
liquors produced in Ex. 3, Ex. 4, and the control, Ex. 9. Gas chromatography and
mass spec was used to determine the amount of the compounds shown in The
graph in shows ratios of the concentrations of compounds present in the cocoa
liquors of Ex. 3, Ex. 4, and the control, Ex. 9.
shows a flavor profile of six compounds present in the cocoa
liquors produced in Ex. 3, Ex. 4, and the control, Ex. 9. Gas chromatography and
mass spec was used to determine the amount of the compounds shown in The
graph in shows ratios of the concentrations of compounds present in the cocoa
liquors of Ex. 3, Ex. 4, and the control, Ex. 9.
shows a flavor profile of compounds present in the cocoa
liquors produced in Ex. 5, Ex. 6, and the control, Ex. 9. Gas chromatography and
mass spec was used to determine the amount of the compounds shown in The
graph in shows ratios of the concentrations of compounds present in the cocoa
liquors of Ex. 5, Ex. 6, and the control, Ex. 9.
shows a flavor profile of six compounds present in the cocoa
liquors produced in Ex. 5, Ex. 6, and the control, Ex. 9. Gas chromatography and
mass spec was used to determine the amount of the compounds shown in The
graph in shows ratios of the concentrations of compounds present in the cocoa
liquors of Ex. 5, Ex. 6, and the control, Ex. 9.
shows a flavor profile of compounds present in the cocoa
liquors produced in Ex. 7, Ex. 8, and the control, Ex. 9. Gas chromatography and
mass spec was used to determine the amount of the compounds shown in The
graph in shows ratios of the concentrations of compounds present in the cocoa
liquors of Ex. 7, Ex. 8, and the control, Ex. 9.
shows a flavor profile of six compounds present in the cocoa
liquors produced in Ex. 7, Ex. 8, and the control, Ex. 9. Gas chromatography and
mass spec was used to determine the amount of the compounds shown in The
graph in shows ratios of the concentrations of compounds present in the cocoa
liquors of Ex. 7, Ex. 8, and the control, Ex. 9.
shows a flavor profile of compounds present in the cocoa
liquors produced in Ex. 1, Ex. 6, Ex. 7, and Ex. 3. Gas chromatography and mass spec
was used to determine the amount of the compounds shown in The graph in
shows ratios of the concentrations of compounds present in the cocoa liquors
of Ex. 1, Ex. 6, Ex. 7, and Ex. 3.
shows a flavor profile of compounds present in the cocoa
liquors produced in Ex. 2, Ex. 5, Ex. 8, and Ex. 4. Gas chromatography and mass spec
was used to determine the amount of the compounds shown in . The graph in
shows ratios of the concentrations of compounds present in the cocoa liquors
of Ex. 2, Ex. 5, Ex. 8, and Ex. 4.
Example 10. Production of fruity cocoa products with good
fermented cocoa beans. Good fermented cocoa beans were 50% Ghana and 50%Ivory
Coast-1, and a reference sample of 100% Arriba beans was used.
Charges of 2.50 kg of cocoa nibs obtained from the cocoa beans were
sterilized for 30 minutes in a box with open steam at a temperature of 101°C, +/-
0.1°C. The steam flow capacity was 2.4 kg/hr and the injected steam pressure was
almost 0.1 bar. The sterilized nibs having the temperature of 101°C were loaded in a
reactor with jacket heating where the temperature was reduced to 75-78°C. In the
reactor, the nibs were heated to temperature of 90-95°C using the jacket heating.
An acid solution having a temperature of 20°C and 40°C was added
to the nibs in the reactor for the acidification process. The average reaction
temperature of the nibs was 55-95°C. Nib samples were taken after a desired
acidification (reaction) time.
The nib samples 10-15 were roasted in a Retch fluidized bed dryer,
which is a laboratory scale jet roaster. The nib samples 16-21 were roasted in a Miag
Spit which is a direct roasting. During roasting, the moisture content of the nibs was
reduced from 20-30% down to 1-2%. The roasted nibs were fist ground to coarse
liquor with a household coffee mill and subsequently ground to cocoa liquor of a
desired fineness with a Retsch laboratory mortal mill.
A first portion of the fine ground liquor was extracted to obtain fat
free cocoa powder and a second portion of the fine ground liquor was hydraulic
pressed into small cakes and filtered cocoa butter. The cakes were broken into
smaller pieces which were pulverized into cocoa powder with a Retsch cutting mill
using sieves of holes with 0.5 mm.
Samples 10-21 and the reference or control sample 22 were analyzed
for: moisture content in the raw nib (before and after sterilization), the acidified nib,
the roasted nib, and the cocoa liquor; pH of the liquor; aroma compound analysis of
the liquor; and intrinsic color in water of the defatted liquor.
Tables 5A and 5B show process conditions and results for Samples 10-
21. The reagents for Samples 10, 12, 14, and 17 were a phosphoric acid solution (0.64
M) and tap water, and the reagents for Samples 11, 13, 15, 16, and 28-21 were a
gluconic delta lactone acid (GDL) solution (3.0 M) and tap water.
Table 5A.
Sample No. 10 11 12 13 14 15
%GDL added at
20 20
40°C
%H3PO4 added
20 20
at 20°C
Reaction temp of nibs
55 55 55 55 55 55
in reactor (°C)
Reaction time (min) 60 60 180 180 120 120
Moisture content
of nibs (%)
Raw nib 8.07 7.94 8.07 7.94 8.07 7.94
After sterilization 14.14 16.14 14.14 16.14 14.14 16.14
After acidification 27.27 25.17 26.16 24.95 27.06 23.63
After Roasting 2.97 3.12 2.47 3.50 2.14 2.75
Liquor
pH 4.82 4.88 4.54 4.56 4.61 4.64
Moisture content (%) 0.8 0.82 0.92 0.78 0.88 0.83
Jet roasting (fluidized
X X X X X X
bed dryer)
Miag Spit roasting
(direct contact roasting)
Table 5B.
Sample No. 16 17 18 19 20 21
%GDL added at
20 20 10 10
40°C
%H PO added
at 20°C
Reaction temp of nibs
55 55 80 80 80 80
in reactor (°C)
Reaction time (min) 180 180 90 180 180 90
Moisture content
of nibs (%)
Raw nib 7.84 7.84 7.81 7.81 7.65 7.65
After sterilization 12.82 13.14 13.47 13.47 14.47 14.47
After acidification 23.57 25.45 23.36 22.83 18.55 19.14
After Roasting 2.49 2.78 3.24 3.60 3.73 3.16
Liquor
pH 4.66 4.56 4.81 4.40 4.86 4.88
Moisture content (%) 0.80 0.82 0.78 0.82 0.70 0.80
Jet roasting (fluidized
bed dryer)
Miag Spit roasting
X X X X X X
(direct contact roasting)
The amount of fruity aroma compounds in the liquor of Samples 10-
21 and the control, Reference Sample 22, Arriba beans, was determined by GCMS
analysis and the amount of such compounds are shown in Tables 6A and 6B. The
amount of each compound is shown in µg/kg.
Table 6A.
Compound Arriba 10 11 12 13 14 15
Ethyl
1.61 14.69 9.91 6.95 10.40 10.02 9.62
methylpropanoate
Ethylmethylbutanoate 4.42 30.17 22.03 18.23 26.36 21.29 22.75
Ethylmethylbutanoate 6.93 38.54 28.83 22.94 33.80 26.89 28.93
Phenylacetaldehyde 23.71 23.64 55.27 51.29 51.63 70.25 54.25
Furaneol 73.65 1467.25 1729.10 866.13 1791.88 1770.40 852.40
Table 6B.
Compound Arriba 16 17 18 19 20 21
Ethyl
1.61 14.50 11.98 8.33 6.48 12.69 10.57
methylpropanoate
Ethylmethylbutanoate 4.42 29.09 25.56 20.32 17.56 29.66 26.00
Ethylmethylbutanoate 6.93 38.45 34.01 25.89 22.91 38.41 33.07
Phenylacetaldehyde 23.71 342.96 141.50 170.65 245.63 129.27 496.35
Furaneol 73.65 1967.78 1251.22 1763.02 1327.92 2927.81 1447.25
[00138] shows the concentrations of the fruity compounds of Tables
6A and 6B in graphical form.
A ratio of the concentrations of the fruity compounds of Tables 6A
and 6B using Arriba as a reference are shown in Tables 7A and 7B.
Table 7A.
Compound Arriba 10 11 12 13 14 15
Ethylmethylpropanoate 1.00 9.14 6.17 4.32 6.47 6.23 5.98
Ethylmethylbutanoate 1.00 6.83 4.99 4.13 5.97 4.82 5.15
Ethylmethylbutanoate 1.00 5.56 4.16 3.31 4.88 3.88 4.18
Phenylacetaldehyde 1.00 1.00 2.33 2.16 2.18 2.96 2.29
Furaneol 1.00 19.92 23.48 11.76 24.33 24.04 11.57
Table 7B.
Compound Arriba 16 17 18 19 20 21
Ethylmethylpropanoate 1.00 9.02 7.45 5.18 4.03 7.89 6.57
Ethylmethylbutanoate 1.00 6.59 5.79 4.60 3.98 6.71 5.89
Ethylmethylbutanoate 1.00 5.55 4.91 3.74 3.31 5.54 4.77
Phenylacetaldehyde 1.00 14.46 5.97 7.20 10.36 5.45 20.93
Furaneol 1.00 26.72 16.99 23.94 18.03 39.75 19.65
shows a spider graph of the ratios of fruity compounds of
Tables 7A and 7B.
Example 11. Compound coatings produced with fruity cocoa
products.
Three compound coatings were produced using the fruity cocoa
powder of Example 3. The formulations of the three compound coatings are shown
in Tables 8-10.
Table 8. Yoghurt compound coating.
Sugar 41.00%
Palm Kernel Stearin 34.00%
Whey Powder 10.00%
fruity cocoa powder Example 3 6.50%
Lactose 5.00%
lecithin 0.50%
D-13 Yoghurt Powder 3.00%
total 100.00%
Table 9. Compound coating with fruity cocoa powder.
Sugar 54.00%
Palm Kernel Stearin 29.00%
fruity cocoa powder Example 3 16.50%
lecithin 0.50%
total 100.00%
Table 10. Limon compound coating with fruity cocoa powder.
Sugar 53.85%
Palm Kernel Stearin 29.00%
fruity cocoa powder Example 3 16.50%
lecithin 0.50%
Lime flavouring 0.15%
total 100.00%
A sensory test was done to compare the limon compound coating of
Table 10 produced with the fruity cocoa powder of Example 3 and a reference limon
compound coating made with commercially available cocoa powder using the
formulation of Table 10. The limon compound coating with the fruity cocoa powder
had more acidity/fruity flavors, more bitterness, more bouquet, more sweet, and
more aromatic flavors as compared to the reference limon compound coating using
the commercially available cocoa powder.
Example 12. Production of fruity cocoa products with good fermented
cocoa beans using various acids. Good fermented cocoa beans were 50% Ghana and
50%Ivory Coast-1.
The cocoa products produced in this Example were produced in
substantially the same manner as the process described in Example 10, but using the
acids in the amounts listed in Table 11.
[00151] Table 11. Acids and color values of powders.
Sample L-value C-value H-value a-value b-value pH
Reference 24.88 28.59 55.34 16.26 23.62 5.82
-natural, not treated with
acid
or alkali
Ascorbic acid 25.23 29.35 53.80 17.33 23.68 4.46
0.5 M
H PO (1.55%) 26.65 27.58 53.68 16.33 22.22 4.67
-by weight
NaHSO (5.7%) 24.02 29.08 49.97 18.70 22.27 3.50
-by weight
GDL (0.5 M) 24.57 27.37 53.37 16.33 21.97 4.56
Example 13. Production of fruity cocoa products with good fermented
cocoa beans using gluconic acid. Good fermented cocoa beans were 50% Ghana and
50%Ivory Coast-1.
[00153] Charges of 10,000 kg of cocoa nibs obtained from the cocoa beans
were pre-heated with open steam pressure of 0.5 bar to a temperature of 100-105ºC
for 3-5 minutes. The 10,000 kg, pre-heated cocoa nib charges were placed into five
different blenders and sterilized for 30 minutes with open steam at a steam pressure
of 0.5 bar and a temperature of 100-105°C. After sterilization, 10% by weight of a 50%
by weight solution of gluconic acid delta lactone having a temperature of 27-30°C
was added to the cocoa nibs in the blender and the acidification process was started.
The addition of the gluconic acid delta lactone solution slowly dropped the
temperature of the cocoa nibs from 95°C to 88°C. No steam was added during the
acidification process.
[00154] No air was injected into blenders 1-4 during the acidification process
and blender 5 did have air injected. The acidification time was 90 minutes and the
average reaction temperature of the nibs during the acidification process was 75-90°C
for blenders 1-4. In blender 5, air was injected for 45 minutes according to the
following schedule: 0-15 minutes, no air injection; 15-30 minutes, air was injected; 30-
45 minutes, no air injection; 45-60 minutes, air was injected; 60-75 minutes, no air
injection; and 75-90 minutes, air was injected.
The acidified nibs were roasted with a constant capacity of 4500
kg/hr. The roasted nibs were ground in a Buhler mill and a ball mill to produce
cocoa liquor of the desired fineness. The pH, moisture content, intrinsic color in
water of the defatted liquor, and presence of fruity flavor compounds were measured
for the cocoa liquor. The cocoa liquor was also pressed into dry cakes having about
11% fat, and the dry cakes were also processed into cocoa powder. The pH, moisture
content, intrinsic color in water, and presence of fruity flavor compounds were
measured for the cocoa powder. During the process, samples were taken every hour.
A summary of the process conditions ; pH, moisture content, and fat
content of the cocoa liquor; and free fatty acid and iodine value of the cocoa butter
produced are shown in Table 12.
Table 12. Process conditions and results of measurements.
Blender No. 1 2 3 4 5
Acidification time 90 90 90 90 90
(minutes)
Gluconic acid (50% by weight solution) 10 10 10 10 10
added
Blower time (minutes) 0 0 0 0 45
Nibs
Moisture content of raw nib (%) 7 7 7 7 7
Moisture content of acidified nib (%) 15.9 14.34 14.07 14.35 12.63
Moisture content after 2 dryer (%) 2.0-2.5 2.0-2.5 2.0-2.5 2.0-2.5 2.0-2.5
Moisture content after nib cooler (%) 1.90 1.80 1.60 1.70 1.70
Cocoa liquor produced
pH 4.7 4.6 4.5 4.4 4.4
Moisture content (%) 1.2 1.1 1.1 1.1 1
Fat content (%) 51.3 51.6 52.2 51.9 51.5
Butter produced
Free Fatty Acid (%) 1.7 1.7 1.7 1.6 1.6
Iodine Value 34.3 34.3 34.3 34.3 34.3
A summary of the percent moisture in the nib and liquor, percent fat
in the liquor, pH of the liquor, and intrinsic color of the liquor in water are shown in
Table 13.
Table 13. Analysis of the cocoa liquor produced at various time
intervals during the process.
Sampling Start of 1 hour 2 3 hours 4 hours 5 hours 6.5 6.75 Reference Sample
time process hours hours hours Natural liquor
% moisture 2.33 1.61 1.74 2.13 1.66 1.56 1.92 1.68 1.5
in nib after
nib cooler
% moisture 1.27 1.06 1.03 1.08 1.07 1.08 1.08 1.01 1.01
in liquor
produced
% fat in 50.61 52.01 51.25 52.1 52.1 52.37 51.9 51.52 54.89
liquor
pH liquor 4.84 4.61 4.55 4.57 4.46 4.41 4.43 4.40 5.58
Intrinsic
color in
water
L 23.30 24.23 24.35 24.84 24.87 24.78 24.74 24.90 26.42
C 23.49 24.05 24.41 24.64 24.54 24.93 25.08 24.81 24.80
H 53.90 54.23 52.24 54.49 54.51 53.82 53.97 54.12 54.42
a 13.84 14.06 14.26 14.31 14.25 14.72 14.75 14.54 14.43
b 18.98 19.51 19.81 20.06 19.98 20.12 20.28 20.10 20.17
The average pH of the cocoa liquor during the run was about 4.65, the
average fat content in the cocoa liquor during the run was about 51.7%, the average
moisture content of the nib after the nib cooler was about 1.82%, and the average
moisture content of the liquor produced during the run was about 1.08%. The color
values of the cocoa liquor produced are comparable with those of the reference,
natural liquor.
[00161] A summary of the percent moisture in the cocoa powder, percent fat
in the cocoa powder, pH of the cocoa powder, and intrinsic color of the cocoa
powder in water are shown in Table 13.
Table 13. Analysis of the cocoa powder produced at various time
intervals during the process. “ffd” refers to fat free dry matter or fat free cocoa
powder.
Sampling Start of 1 hour 2 3 hours 4 hours 5 hours 6.5 6.75 Reference Sample
time process hours hours hours Natural liquor
% moisture 3.45 3.04 2.99 3.57 3.91 3.02 2.79 2.53 4.04
powder
% fat in 12.48 11.50 10.69 10.74 10.70 10.93 11.35 11.31 20.80
powder
pH 4.72 4.54 4.47 4.52 4.45 4.48 4.47 4.60 5.60
powder
Intrinsic
color in
water of
powder
L 21.78 23.21 23.87 25.21 23.85 23.96 23.94 24.84 25.72
C 23.35 23.81 24.51 26.35 24.21 24.90 24.89 26.44 25.18
H 52.99 53.70 53.70 53.49 54.00 53.31 53.33 54.09 54.06
a 14.06 14.11 14.51 15.68 14.23 14.88 14.87 15.51 14.78
b 18.65 19.21 19.75 21.18 19.58 19.97 19.96 21.51 20.39
Intrinsic
color in
water of
powder
L 19.82 21.39 22.14 23.36 22.00 22.19 22.15 23.06 22.30
C 22.41 22.99 23.72 25.50 23.36 24.09 24.07 25.60 23.67
H 52.72 53.42 53.43 53.17 53.71 53.03 53.04 53.78 53.50
a 13.57 13.70 14.13 15.29 13.83 14.49 14.47 15.12 14.08
b 17.83 18.46 19.05 20.41 18.83 19.24 19.23 20.65 19.03
The average pH of the cocoa powder produced from the cocoa liquor
was about. 4.53. The color values of the cocoa powder produced are comparable to
those of the reference sample, natural liquor.
A summary of cocoa powders and pulverized cakes made from cocoa
liquors during the process are shown in Table 14.
Table 14. Comparison of cocoa powders produced.
Sample % % fat pH L ffd C ffd H ffd L C H
Description moisture
Pulverized cakes 3.08 11.71 4.53 21.48 23.76 53.87 23.03 24.65 54.15
Made from liquor at
3 hours after
process
began
Pulverized cakes 2.69 10.58 4.48 22.36 24.73 53.74 24.04 25.52 53.91
Made from liquor at
6.75 hours after
Process began
Pulverized cakes 2.98 11.03 4.64 20.7 24.1 54.04 22.42 24.98 54.30
from one press
machine
Pulverized cakes 3.06 12.64 4.64 20.68 24.62 53.95 22.63 25.63 54.25
from other press
machine
Pulverized cakes 3.41 12.64 5.20 18.44 22.19 53.74 20.30 23.18 53.99
From one
batchmaker
Pulverized cakes 3.05 12.34 4.94 19.33 22.92 53.91 21.19 23.88 54.17
From other
batchmaker
Final powder from 4.40 12.38 4.85 19.48 23.34 53.89 21.54 24.41 54.18
One batchmaker
Final powder from 4.70 12.73 5.05 18.30 22.57 53.52 20.39 23.69 53.82
Other batchmaker
Reference Sample 4.40 20.80 5.6 22.30 23.67 53.50 25.72 25.18 54.06
The microbiological results of the final powders produced were good
and all within commercially acceptable limits for cocoa powders.
An SGS analysis on a cocoa powder produced is shown in Table 15.
Table 15. SGS analysis on cocoa powder.
Ash content (%) 6.59
Total alkalinity (ml/100g) 83.67
Total iron as Fe (mg/kg) 280
Potassium as K (%) 2.5
Sodium as Na (%) 0.005
Aluminum as Al (mg/kg) 89
Silicium as Si (%) <0.01
Citric acid (%) 0.97
Acetic acid (%) 0.45
Lactic acid (%) 0.33
OchraToxin A (µg/kg) 0.3
Acrylamide (µg/kg) 230
The values of Fe, Al, Si, and acrylamide in the cocoa powders of the
present invention are much lower than those measured in natural powders typically
produced.
The quality of the cocoa butters produced according to this example is
good and within commercially acceptable limits.
A ratio of the concentrations of the fruity compounds of the cocoa
liquor produced at various timepoints during the process compared to the reference,
Arriba is shown in Table 16. The fruity flavor compounds were present in the cocoa
liquor at between about: 3.28-4.26 µg/kg of ethylmethylpropanoate; 9.37-10.82
µg/kg of ethylmethylbutanoate; 12.95-14.55 µg/kg of ethylmethylbutanoate;
220.03-269.58 µg/kg of phenylacetaldehyde; and 1257.21-1938.47 µg/kg of furaneol.
Table 16. Fruity compound analysis, Arriba as reference.
Sample Arriba 1 2 3 4 5 6 7 8
Start of 1 hr 2 hrs 3 hrs 4 hrs 5 hrs 6.5 hrs 6.75
Time (hr)
Process hrs
:30
Ethyl 1 2.43 2.62 2.43 2.04 2.37 2.51 2.65 2.27
methylpropanoate
Ethylmethylbutanoate 1 2.22 2.36 2.45 2.32 2.31 2.29 2.36 2.12
Ethylmethylbutanoate 1 1.95 2.07 2.10 2.06 1.99 1.96 2.05 1.87
phenylacetaldehyde 1 10.31 11.37 10.87 10.21 9.28 9.37 10.85 9.81
furaneol 1 17.07 21.49 24.73 23.39 26.32 20.09 23.66 22.92
shows a graph of the ratio of the concentrations of the fruity
compounds of Table 16, and a spider graph of the concentrations of Table 16 is
shown in .
A ratio of the concentrations of the fruity compounds of the cocoa
liquor produced at various timepoints during the process compared to the reference,
a natural liquor of 50% Ghana and 50% Ivory Coast beans is shown in Table 17.
[00175] Table 17. Fruity compound analysis, natural liquor as reference.
Sample Natural 1 2 3 4 5 6 7 8
liquor
Start of 1 hr 2 hrs 3 hrs 4 hrs 5 hrs 6.5 hrs 6.75
Time (hr)
Process hrs
:30
Ethyl 1 27.59 29.77 27.58 23.13 26.96 28.44 30.13 25.73
methylpropanoate
Ethylmethylbutanoate 1 5.40 6.58 6.35 4.88 7.55 5.68 6.42 5.89
Ethylmethylbutanoate 1 4.69 4.88 5.65 4.43 5.46 4.70 5.37 5.00
phenylacetaldehyde 1 27.59 29.77 27.58 23.13 26.96 28.44 30.13 25.73
furaneol 1 30.77 32.69 33.97 32.07 31.97 31.75 32.69 29.40
shows a graph of the ratio of the concentrations of the fruity
compounds of Table 16, and a spider graph of the concentrations of Table 17 is
shown in .
[00177] A ratio of the concentrations of the fruity compounds of the cocoa
liquor obtained from nibs from the nib cooler produced at various timepoints during
the process compared to the reference, Arriba is shown in Table 18. The fruity flavor
compounds were present in the cocoa liquor at between about: 4.63-8.85 µg/kg of
ethylmethylpropanoate; 17.02-20.55 µg/kg of ethylmethylbutanoate; 23.15-
27.44 µg/kg of ethylmethylbutanoate; 316.53-435.79 µg/kg of phenylacetaldehyde;
and 1710.89-2366.37 µg/kg of furaneol.
Table 18. Fruity compound analysis of cocoa nibs from nib cooler,
Arriba as reference.
Sample Arriba 1 2 3 4 5 6 7 8
Start of 1 hr 2 hrs 3 hrs 4 hrs 5 hrs 6.5 hrs 6.75
Time (hr)
Process hrs
:30
Ethyl 1 5.50 5.05 4.97 3.79 2.88 5.31 4.37 3.40
methylpropanoate
Ethylmethylbutanoate 1 4.65 4.22 4.58 4.28 3.85 4.65 3.86 3.91
Ethylmethylbutanoate 1 3.93 3.64 3.93 3.70 3.37 3.96 3.34 3.42
phenylacetaldehyde 1 13.36 13.77 15.35 13.35 15.15 15.90 18.35 15.82
furaneol 1 23.23 26.20 32.13 26.73 26.12 29.80 26.28 27.24
[00179] shows a graph of the ratio of the concentrations of the fruity
compounds of Table 18.
Example 14. Production of dark chocolate with fruity flavored cocoa
products.
Dark chocolate was made with the following ingredients: 37.18% of a
fruity flavored cocoa liquor of the present invention; 22.46% of cocoa butter; 14% of a
fruity flavored cocoa powder of the present invention; 25.85% of sugar; 0.5% of soy
lecithin; and 0.01% of vanillin. The dark chocolate was about 72% cocoa. The
chocolate was produced using a method conventionally known by one of ordinary
skill in the art.
[00182] Dark chocolate was made with the following ingredients: 49.75% of a
fruity flavored cocoa liquor of the present invention; 49.74% of sugar; 0.5% of soy
lecithin; and 0.01% of natural vanilla. The dark chocolate was about 48% cocoa. The
chocolate was produced using a method conventionally known by one of ordinary
skill in the art.
[00183] Dark chocolate was made with the following ingredients: 64.5% of a
fruity flavored cocoa liquor of the present invention; 9% of cocoa butter; 26% of
sugar; and 0.5% of sunflower lecithin. The dark chocolate was about 71% cocoa. The
chocolate was produced using a method conventionally known by one of ordinary
skill in the art.
[00184] Dark chocolate with a raspberry powder was made with the
following ingredients: 37.18% of a fruity flavored cocoa liquor of the present
invention; 22.46% of cocoa butter; 5% of a raspberry powder; 14% of a fruity flavored
cocoa powder of the present invention; 20.85% of sugar; 0.5% of soy lecithin; and
0.01% of vanillin. The raspberry flavored chocolate was about 72% cocoa. The
chocolate was produced using a method conventionally known by one of ordinary
skill in the art.
Example 14. Production of a filling.
A yoghurt/strawberry filling was made with the following
ingredients: 31.35% of a cocoa butter equivalent (CBE); 7.5% of skimmed milk
powder; 3% of whole milk powder; 2% of strawberry flakes; 7.5% of whey powder;
0.6% of lactose; 47.4% of sugar; 0.6% of soy lecithin; and 0.05% of natural vanilla. The
filling was produced using a method conventionally known by one of ordinary skill
in the art.
Example 15. Production of a candy with a fruity flavored cocoa
product.
Pralines were produced using the yoghurt/strawberry filling of
Example 14 and a chocolate of Example 13 as a shell using techniques known by
those of ordinary skill in the art.
Example 16. Production of a candy with a fruity flavored cocoa
product.
A yogurt/cocoa filling was produced using between 3-7% of a fruity
flavored cocoa powder of the present invention. A praline was produced using the
yogurt/cocoa filling and a chocolate of Example 13 as a shell.
Example 17. Production of a cake with a fruity flavored cocoa
product.
A cake was produced with the following ingredients: 250 grams of
egg; 170 grams of sugar; 80 grams of flour; 80 grams of cornstarch; and 20 grams of a
fruity flavored cocoa powder of the present invention. The cake was produced using
a technique known by one of ordinary skill in the art.
Example 18. Production of a cheesecake with a fruity flavored cocoa
product.
Cheesecakes were produced with the following ingredients: 575
grams of curt cheese; 5 grams of egg yolk; 57.5 grams of flour; 76 grams of cornstarch;
a sufficient quantity of milk; 5 grams of egg whites; 115 grams of sugar; and 2.5-10%
of a fruity flavored cocoa powder of the present invention. The cheesecakes were
produced using techniques known by those of ordinary skill in the art.
Example 19. Production of a chocolate filling.
[00196] A chocolate filling was produced with the following ingredients:
38.9% of sugar; 5% of sunflower oil; 10% of whey powder; 22.5% of palm oil; 8% of
white lactose; 7% of a fruity cocoa liquor of the present invention; 5% of skimmed
milk powder; 3% of a fruity cocoa powder of the present invention; and 0.6% of soy
lecithin. The chocolate filling was produced using techniques known by those of
ordinary skill in the art.
This disclosure has been described with reference to certain
exemplary embodiments, compositions and uses thereof. However, it will be
recognized by those of ordinary skill in the art that various substitutions,
modifications or combinations of any of the exemplary embodiments may be made
without departing from the spirit and scope of the disclosure. Thus, the disclosure is
not limited by the description of the exemplary embodiments, but rather by the
appended claims as originally filed.
[00198] In this specification where reference has been made to patent
specifications, other external documents, or other sources of information, this is
generally for the purpose of providing a context for discussing the features of the
invention. Unless specifically stated otherwise, reference to such external documents
is not to be construed as an admission that such documents, or such sources of
information, in any jurisdiction, are prior art, or form part of the common general
knowledge in the art.
In the description in this specification reference may be made to
subject matter that is not within the scope of the claims of the current application.
That subject matter should be readily identifiable by a person skilled in the art and
may assist in putting into practice the invention as defined in the claims of this
application.
Claims (31)
1. A cocoa product selected from the group consisting of a cocoa powder, a cocoa liquor, and a cocoa butter, the cocoa product having a fruity flavor 5 comprising: an increased amount of a fruity aroma compounds, wherein the fruity aroma compounds are selected from the group consisting of furaneol, phenylacetaldehyde, ethylmethylpropanoate, ethylmethylbutanoate, ethylmethylbutanoate, and combinations of any thereof; wherein the cocoa product comprises an amount of 10 fruity aroma compounds selected from the group consisting of at least 5 µg/kg of ethylmethylpropanoate, at least 15 µg/kg of ethylmethylbutanoate, at least 20 µg/kg of ethylmethylbutanoate, at least 50 µg/kg of phenylacetaldehyde, at least 100 µg/kg of furaneol, and combinations of any thereof.
2. The cocoa product of claim 1, wherein the cocoa product comprises an 15 amount of fruity aroma compounds selected from the group consisting of at least 2.5 µg/kg of ethylmethylpropanoate, at least 7.5 µg/kg of ethylmethylbutanoate, at least 10 µg/kg of ethylmethylbutanoate, at least 50 µg/kg of phenylacetaldehyde, at least 100 µg/kg of furaneol, and combinations of any thereof.
3. The cocoa product of claim 1, wherein the cocoa product is cocoa 20 powder.
4. The cocoa product of claim 1, wherein the cocoa product is cocoa liquor.
5. The cocoa product of claim 1, wherein the cocoa product has a color value selected from the group consisting of an L value of between about 22 to about 25 29, a C value of about 23 to about 30, an H value of between about 35 to about 55, and combinations of any thereof.
6. The cocoa product of claim 1, wherein the cocoa product has a color value selected from the group consisting of an L value of between about 18 to about 29, a C value of about 23 to about 30, an H value of between about 35 to about 55, and combinations of any thereof.
7. The cocoa product of claim 1, wherein the cocoa product has a pH of between about 4.5 to about 6. 5
8. The cocoa product of claim 1, wherein the cocoa product has a pH of between about 4.5 to about 5.
9. The cocoa product of claim 1, wherein the cocoa product has been roasted.
10. The cocoa product of claim 1, wherein the cocoa product originates 10 from un-fermented cocoa beans, under fermented cocoa beans, good fermented cocoa beans, or combinations of any thereof.
11. The cocoa product of claim 1, wherein the cocoa product originates from good fermented cocoa beans.
12. The cocoa product of claim 12, wherein the cocoa product has less 15 bitterness as compared to cocoa products originating from un-fermented cocoa beans, under-fermented cocoa beans, or a combination thereof.
13. A food product comprising the cocoa product of claim 1.
14. A method for producing the cocoa product having a fruity flavor of claim 1, the method comprising: 20 mixing cocoa nibs, de-shelled cocoa beans, or a combination thereof with an acid and water; and roasting the acidified nibs, the acidified, de-shelled cocoa beans, or the combination thereof; wherein the cocoa nibs, the de-shelled cocoa beans, or the combination thereof are good fermented. 25
15. The method according to claim 14, further comprising washing the acidified cocoa nibs, the acidified de-shelled cocoa beans, or the combination thereof with water.
16. The method according to claim 14, wherein the acid is selected from the group consisting of gluconic delta lactone acid, phosphoric acid, ascorbic acid, sodium bisulphate acid, and combinations of any thereof.
17. The method according to claim 14, wherein the cocoa nibs, the de- 5 shelled cocoa beans, or the combination thereof are under fermented, un-fermented, or a combination thereof.
18. The method according to claim 14, further comprising sterilizing the cocoa nibs, the de-shelled cocoa beans, or the combination thereof.
19. The method according to claim 14, wherein the nibs, the de-shelled 10 cocoa beans, or the combination thereof are in contact with the acid and water for a time of between about 0.5 to about 4 hours.
20. The method according to claim 14, wherein the nibs, the de-shelled cocoa beans, or the combination thereof are in contact with the acid and the water at a temperature of between about 15°C and about 90°C. 15
21. The method according to claim 14, further comprising grinding the roast nibs, the roast de-shelled cocoa beans, or the combination thereof thus producing cocoa liquor.
22. The method according to claim 21, further comprising separating the cocoa liquor into cocoa butter and cocoa presscake. 20
23. The method according to claim 22, further comprising grinding the cocoa presscake into cocoa powder.
24. The method according to claim 21, further comprising defatting the cocoa liquor.
25. The method according to claim 14, wherein the acidified nibs, the 25 acidified de-shelled cocoa beans, or the combination thereof are roasted to a moisture content of less than about 2%.
26. The method according to claim 14, where the roasted, acidified nibs, the roasted, acidified de-shelled cocoa beans, or the combination thereof comprise an amount of fruity aroma compounds selected from the group consisting of at least 2.5 µg/kg of ethylmethylpropanoate, at least 7.5 µg/kg of ethylmethylbutanoate, at least 10 µg/kg of ethylmethylbutanoate, at least 50 µg/kg of phenylacetaldehyde, at least 100 µg/kg of furaneol, and combinations of any thereof.
27. The method according to claim 14, wherein the roasted, acidified nibs, 5 the roasted, acidified, de-shelled cocoa beans, or the combination thereof have a color value selected from the group consisting of an L value of between about 18 to about 29, a C value of about 23 to about 30, an H value of between about 35 to about 55, and combinations of any thereof.
28. The method according to claim 14, wherein the nibs, the de-shelled 10 cocoa beans, or the combination thereof in the acid and water have a pH of between about 4.5 to about 6.
29. A cocoa product as claimed in claim 1 substantially as herein described or exemplified and with or without reference to the accompanying drawings.
30. A food product as claimed in claim 13 substantially as herein described 15 or exemplified and with or without reference to the accompanying drawings.
31. A method as claimed in claim 14 substantially as herein described or exemplified and with or without reference to the accompanying drawings.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161473246P | 2011-04-08 | 2011-04-08 | |
US61/473,246 | 2011-04-08 | ||
PCT/US2012/032711 WO2012139096A1 (en) | 2011-04-08 | 2012-04-09 | Fruity flavored cocoa products and processes for producing such cocoa products |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ616399A NZ616399A (en) | 2015-08-28 |
NZ616399B2 true NZ616399B2 (en) | 2015-12-01 |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20190335783A1 (en) | Fruity flavored cocoa products and processes for producing such cocoa products | |
AU2018200104B2 (en) | Process for producing dark brown natural cocoa | |
AU2018200103B2 (en) | Processes for producing dark red and dark brown natural cocoa | |
NZ616399B2 (en) | Fruity flavored cocoa products and processes for producing such cocoa products | |
OA16613A (en) | Fruity flavored cocoa products and processes for producing such cocoa products. | |
NZ716179B2 (en) | Processes for producing dark brown natural cocoa | |
OA17652A (en) | Process for producing dark brown natural cocoa. | |
NZ716180B2 (en) | Processes for producing dark red and dark brown natural cocoa | |
OA17653A (en) | Processes for producing dark red and dark brown natural cocoa. |