JP2019037962A - Method of reforming organic waste - Google Patents
Method of reforming organic waste Download PDFInfo
- Publication number
- JP2019037962A JP2019037962A JP2017163854A JP2017163854A JP2019037962A JP 2019037962 A JP2019037962 A JP 2019037962A JP 2017163854 A JP2017163854 A JP 2017163854A JP 2017163854 A JP2017163854 A JP 2017163854A JP 2019037962 A JP2019037962 A JP 2019037962A
- Authority
- JP
- Japan
- Prior art keywords
- organic waste
- water
- soluble polymer
- monomer
- mass
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000010815 organic waste Substances 0.000 title claims abstract description 46
- 238000000034 method Methods 0.000 title claims abstract description 22
- 238000002407 reforming Methods 0.000 title claims abstract description 15
- 239000000178 monomer Substances 0.000 claims abstract description 51
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 42
- 239000004815 dispersion polymer Substances 0.000 claims abstract description 35
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 20
- 239000002270 dispersing agent Substances 0.000 claims abstract description 16
- 239000000203 mixture Substances 0.000 claims abstract description 15
- 239000012266 salt solution Substances 0.000 claims abstract description 11
- 238000003756 stirring Methods 0.000 claims abstract description 7
- 238000012674 dispersion polymerization Methods 0.000 claims abstract description 5
- 238000002156 mixing Methods 0.000 claims abstract description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 239000007864 aqueous solution Substances 0.000 claims description 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 6
- 150000001450 anions Chemical class 0.000 claims description 6
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 6
- 239000000920 calcium hydroxide Substances 0.000 claims description 6
- 235000011116 calcium hydroxide Nutrition 0.000 claims description 6
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 235000011121 sodium hydroxide Nutrition 0.000 claims description 3
- 239000005416 organic matter Substances 0.000 claims description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 2
- 235000011118 potassium hydroxide Nutrition 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- 235000011181 potassium carbonates Nutrition 0.000 claims 1
- 235000017550 sodium carbonate Nutrition 0.000 claims 1
- 229920000642 polymer Polymers 0.000 abstract description 24
- 238000011282 treatment Methods 0.000 abstract description 11
- 230000002776 aggregation Effects 0.000 abstract description 5
- 239000003513 alkali Substances 0.000 abstract description 5
- 244000144977 poultry Species 0.000 abstract description 4
- 238000004220 aggregation Methods 0.000 abstract description 3
- 239000000243 solution Substances 0.000 abstract description 3
- 230000004931 aggregating effect Effects 0.000 abstract description 2
- 238000009304 pastoral farming Methods 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 description 16
- 239000010802 sludge Substances 0.000 description 15
- 239000007788 liquid Substances 0.000 description 14
- 239000002699 waste material Substances 0.000 description 14
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 150000003839 salts Chemical class 0.000 description 10
- 125000002091 cationic group Chemical group 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 9
- 125000000129 anionic group Chemical group 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 244000144972 livestock Species 0.000 description 8
- 241001465754 Metazoa Species 0.000 description 7
- 239000003999 initiator Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 150000001768 cations Chemical class 0.000 description 5
- -1 dimethylaminoethyl Chemical group 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- FZGFBJMPSHGTRQ-UHFFFAOYSA-M trimethyl(2-prop-2-enoyloxyethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCOC(=O)C=C FZGFBJMPSHGTRQ-UHFFFAOYSA-M 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 230000003472 neutralizing effect Effects 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229920006317 cationic polymer Polymers 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 239000003337 fertilizer Substances 0.000 description 3
- 239000004310 lactic acid Substances 0.000 description 3
- 235000014655 lactic acid Nutrition 0.000 description 3
- 239000010871 livestock manure Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920002401 polyacrylamide Polymers 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 235000013594 poultry meat Nutrition 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000010865 sewage Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 241000283690 Bos taurus Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 241000283086 Equidae Species 0.000 description 2
- 241000287828 Gallus gallus Species 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- 241001494479 Pecora Species 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 241000282887 Suidae Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- LXEKPEMOWBOYRF-UHFFFAOYSA-N [2-[(1-azaniumyl-1-imino-2-methylpropan-2-yl)diazenyl]-2-methylpropanimidoyl]azanium;dichloride Chemical compound Cl.Cl.NC(=N)C(C)(C)N=NC(C)(C)C(N)=N LXEKPEMOWBOYRF-UHFFFAOYSA-N 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- 239000010828 animal waste Substances 0.000 description 2
- ZGCZDEVLEULNLJ-UHFFFAOYSA-M benzyl-dimethyl-(2-prop-2-enoyloxyethyl)azanium;chloride Chemical compound [Cl-].C=CC(=O)OCC[N+](C)(C)CC1=CC=CC=C1 ZGCZDEVLEULNLJ-UHFFFAOYSA-M 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 235000013330 chicken meat Nutrition 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 210000003608 fece Anatomy 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 229920000831 ionic polymer Polymers 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 238000002715 modification method Methods 0.000 description 2
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 2
- RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 description 2
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000000979 retarding effect Effects 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- FVQMJJQUGGVLEP-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOC(C)(C)C FVQMJJQUGGVLEP-UHFFFAOYSA-N 0.000 description 1
- XLPJNCYCZORXHG-UHFFFAOYSA-N 1-morpholin-4-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCOCC1 XLPJNCYCZORXHG-UHFFFAOYSA-N 0.000 description 1
- VBZBISQOWJYWCC-UHFFFAOYSA-N 2-(2-carboxypropan-2-yldiazenyl)-2-methylpropanoic acid Chemical compound OC(=O)C(C)(C)N=NC(C)(C)C(O)=O VBZBISQOWJYWCC-UHFFFAOYSA-N 0.000 description 1
- AVTLBBWTUPQRAY-UHFFFAOYSA-N 2-(2-cyanobutan-2-yldiazenyl)-2-methylbutanenitrile Chemical compound CCC(C)(C#N)N=NC(C)(CC)C#N AVTLBBWTUPQRAY-UHFFFAOYSA-N 0.000 description 1
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 1
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
- AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 description 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
- LTHJXDSHSVNJKG-UHFFFAOYSA-N 2-[2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCOC(=O)C(C)=C LTHJXDSHSVNJKG-UHFFFAOYSA-N 0.000 description 1
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 1
- VMSBGXAJJLPWKV-UHFFFAOYSA-N 2-ethenylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=C VMSBGXAJJLPWKV-UHFFFAOYSA-N 0.000 description 1
- FVPMLCUKLBYBSV-UHFFFAOYSA-M 2-hydroxypropyl-dimethyl-(prop-2-enoyloxymethyl)azanium;chloride Chemical compound [Cl-].CC(O)C[N+](C)(C)COC(=O)C=C FVPMLCUKLBYBSV-UHFFFAOYSA-M 0.000 description 1
- RIAVQNCBHNMYFJ-UHFFFAOYSA-M 2-hydroxypropyl-dimethyl-[phenyl(prop-2-enoyloxy)methyl]azanium;chloride Chemical compound [Cl-].CC(O)C[N+](C)(C)C(OC(=O)C=C)C1=CC=CC=C1 RIAVQNCBHNMYFJ-UHFFFAOYSA-M 0.000 description 1
- MKTOIPPVFPJEQO-UHFFFAOYSA-N 4-(3-carboxypropanoylperoxy)-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)OOC(=O)CCC(O)=O MKTOIPPVFPJEQO-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- IRQWEODKXLDORP-UHFFFAOYSA-N 4-ethenylbenzoic acid Chemical compound OC(=O)C1=CC=C(C=C)C=C1 IRQWEODKXLDORP-UHFFFAOYSA-N 0.000 description 1
- RTANHMOFHGSZQO-UHFFFAOYSA-N 4-methoxy-2,4-dimethylpentanenitrile Chemical compound COC(C)(C)CC(C)C#N RTANHMOFHGSZQO-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
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- KYIKRXIYLAGAKQ-UHFFFAOYSA-N abcn Chemical compound C1CCCCC1(C#N)N=NC1(C#N)CCCCC1 KYIKRXIYLAGAKQ-UHFFFAOYSA-N 0.000 description 1
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- 238000004458 analytical method Methods 0.000 description 1
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- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- QBZPCMKUFMJWAN-UHFFFAOYSA-N benzyl-dimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C=CC(=O)NCCC[N+](C)(C)CC1=CC=CC=C1 QBZPCMKUFMJWAN-UHFFFAOYSA-N 0.000 description 1
- NSHHIZQAQLPYLS-UHFFFAOYSA-N butane-1,3-diol;2-methylprop-2-enoic acid Chemical compound CC(O)CCO.CC(=C)C(O)=O NSHHIZQAQLPYLS-UHFFFAOYSA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
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- 230000007423 decrease Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
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- 239000000839 emulsion Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000009313 farming Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- WFKDPJRCBCBQNT-UHFFFAOYSA-N n,2-dimethylprop-2-enamide Chemical compound CNC(=O)C(C)=C WFKDPJRCBCBQNT-UHFFFAOYSA-N 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- IMNDHOCGZLYMRO-UHFFFAOYSA-N n,n-dimethylbenzamide Chemical compound CN(C)C(=O)C1=CC=CC=C1 IMNDHOCGZLYMRO-UHFFFAOYSA-N 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-N 0.000 description 1
- 239000003895 organic fertilizer Substances 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229940085991 phosphate ion Drugs 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- RRHXZLALVWBDKH-UHFFFAOYSA-M trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)OCC[N+](C)(C)C RRHXZLALVWBDKH-UHFFFAOYSA-M 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Treatment Of Sludge (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
本発明は有機性廃棄物の改質方法に関する。更に詳しくは養豚場や養鶏場等の家畜の畜産施設で発生する有機性廃棄物に対して、薬品を添加して改質し固化する処理方法であり、更に詳しくは、アルカリ剤及び特定の組成を有する単量体混合物を、分散剤として塩水溶液に可溶な水溶性高分子を共存させ該塩水溶液中にて撹拌下、分散重合して得られる水溶性高分子分散液散を添加し固化する有機性廃棄物の改質方法に関する。 The present invention relates to a method for modifying organic waste. More specifically, it is a treatment method in which chemicals are added to organic waste generated in livestock facilities such as pig farms and poultry farms to improve and solidify, and more specifically, alkaline agents and specific compositions Water-soluble polymer dispersion liquid dispersion obtained by dispersing and polymerizing a monomer mixture having a water-soluble polymer coexisting in an aqueous salt solution as a dispersant in the aqueous salt solution while stirring is added and solidified. The present invention relates to a method for reforming organic waste.
養豚場や養鶏場等の家畜の畜産施設で発生する有機性廃棄物として、肥料や家畜糞尿、飼料、各種汚泥、生ごみ等が挙げられる。これら有機性廃棄物の内、固形状のものは場外に排出あるいは再利用しやすいが、含水状のものについては改質処理する必要が生じる。これら有機性廃棄物を改質するためにこれまでに様々な薬品添加処方が提案されている。薬品として、一般的にポリアクリルアミド(PAM)系水溶性高分子等が汎用されている。例えば、特許文献1では、有機性廃棄物にポリマーを添加混合した後加熱乾燥し、次いで熱処理する熟成コンポスト様物の製造方法が開示されている。使用するポリマーとして、(メタ)アクリロイルオキシエチルトリメチルアンモニウムクロライドとアクリルアミドとの共重合体のようなカチオン性ポリマー、(メタ)アクリロイルオキシエチルトリメチルアンモニウムクロライドとアクリル酸とアクリルアミドとの共重合体のような両性ポリマー等が記載されている。
特許文献2では、最終液体分及び最終固体分を生成し、最終液体分の浮遊物質(SS)含有量が約3g/L以下である動物肥料の処理方法が開示されており、ポリアクリルアミドを添加することが記載されている。
特許文献3では、動物性廃棄物等の含湿汚泥から揮発性ガスを除去するプロセスが開示されており、脱水効果を高めるための凝集剤として種々のポリマーの使用が記載されている。
特許文献4では、含水率90質量%以上の動物糞尿にリセルロースファイバーを添加し、有機高分子凝集剤を加えてかきまぜ、十分にフロックを形成させ、次いで搾液後、発酵処理するコンポスト肥料の製造方法が開示されており、有機高分子凝集剤として種々のポリマーが記載されている。
しかし、これらは何れも使用するポリマーの有効な組成や物性について記載はない。又、対象物によっては従来の改質処方では、満足した効果が得られない場合が有り、ポリマーを使用する有機性廃棄物の効率的な改質方法が要望されている。
Examples of organic waste generated in livestock facilities for livestock such as pig farms and poultry farms include fertilizers, livestock manure, feed, various sludges, and garbage. Among these organic wastes, solid ones can be easily discharged or reused outside the site, but water-containing ones need to be reformed. Various chemical additive formulations have been proposed to improve these organic wastes. In general, polyacrylamide (PAM) water-soluble polymers are widely used as chemicals. For example, Patent Document 1 discloses a method for producing an aged compost-like product in which a polymer is added to and mixed with organic waste, followed by heat drying, and then heat treatment. The polymer used is a cationic polymer such as a copolymer of (meth) acryloyloxyethyltrimethylammonium chloride and acrylamide, such as a copolymer of (meth) acryloyloxyethyltrimethylammonium chloride, acrylic acid and acrylamide. Amphoteric polymers and the like are described.
Patent Document 2 discloses a method for treating animal fertilizer that produces a final liquid content and a final solid content, and has a suspended solid (SS) content of about 3 g / L or less, and adds polyacrylamide. It is described to do.
Patent Document 3 discloses a process for removing volatile gas from moisture-containing sludge such as animal waste, and describes the use of various polymers as a flocculant for enhancing the dehydration effect.
According to Patent Document 4, compost fertilizer to be fermented by adding re-cellulose fiber to animal manure with a water content of 90% by mass or more, adding an organic polymer flocculant and stirring sufficiently to form floc, and then squeezing. A production method is disclosed, and various polymers are described as organic polymer flocculants.
However, none of these documents describe the effective composition and physical properties of the polymer used. Further, depending on the object, there are cases where a satisfactory effect cannot be obtained with the conventional reforming recipe, and there is a demand for an efficient method for reforming organic waste using a polymer.
本発明の目的は、養豚場、養鶏場等の家畜の畜産施設から発生する有機性廃棄物の改質において、ポリマーを添加し、凝集処理により有機性廃棄物の改質方法を提供することである。 An object of the present invention is to provide a method for reforming organic waste by agglomeration treatment by adding a polymer in reforming organic waste generated from livestock facilities such as pig farms and poultry farms. is there.
本発明者は、前記課題を解決するために鋭意検討の結果、以下に述べる発明に達した。即ち、有機性廃棄物に対して、アルカリ剤及び下記一般式(1)で表される単量体を必須として含有する単量体あるいは単量体混合物を、分散剤として塩水溶液に可溶な水溶性高分子を共存させ該塩水溶液中にて撹拌下、分散重合して得られる水溶性高分子分散液を添加する有機性廃棄物の改質方法である。
一般式(1)
R1は水素又はメチル基、R2、R3は炭素数1〜3のアルキル基あるいはヒドロキシアルキル基、R4は炭素数1〜3のアルキルあるいはアルコキシル基、7〜20のアルキル基あるいはアリール基、Aは酸素またはNH、Bは炭素数2〜4のアルキレン基を表わす、X1 −は陰イオンをそれぞれ表わす。
As a result of intensive studies to solve the above problems, the present inventor has reached the invention described below. That is, a monomer or monomer mixture containing an alkaline agent and a monomer represented by the following general formula (1) as an essential component is soluble in an aqueous salt solution as a dispersant. This is a method for reforming organic waste, in which a water-soluble polymer dispersion obtained by dispersing and polymerizing a water-soluble polymer in the aqueous salt solution with stirring is added.
General formula (1)
R 1 is hydrogen or a methyl group, R 2 and R 3 are alkyl groups or hydroxyalkyl groups having 1 to 3 carbon atoms, R 4 is an alkyl or alkoxyl group having 1 to 3 carbon atoms, and an alkyl group or aryl group having 7 to 20 carbon atoms. , a is oxygen or NH, B represents an alkylene group having 2 to 4 carbon atoms, X 1 - represents respectively an anion.
本発明におけるアルカリ剤及び水溶性高分子分散液を有機性廃棄物に適用することで有機性廃棄物を効率良く改質することができる。 The organic waste can be efficiently modified by applying the alkaline agent and the water-soluble polymer dispersion in the present invention to the organic waste.
本発明における改質方法は、アルカリ剤及び水溶性高分子分散液を家畜の畜産施設から発生する有機性廃棄物に添加、混合し凝集させた後、改質することを特徴とする。一般的に使用されている高分子に比べて、特定の組成を有し、特定の製法により製造されるため、溶解効率が良く、有機性廃棄物に添加すると優れた凝集処理効果を発揮し効率良く改質することができる。改質した廃棄物は、有機質肥料や飼料として再利用することができる。 The modification method in the present invention is characterized in that an alkaline agent and a water-soluble polymer dispersion are added to organic waste generated from livestock facilities for livestock, mixed and aggregated, and then modified. Compared to commonly used polymers, it has a specific composition and is manufactured by a specific manufacturing method, so it has good dissolution efficiency, and when added to organic waste, it exhibits an excellent coagulation effect and efficiency It can be well modified. The modified waste can be reused as organic fertilizer and feed.
本発明における有機性廃棄物は、主に豚、鶏、牛、羊、馬等の家畜の畜産施設から発生する動物用の飼料の余剰や廃棄分、飼育動物の糞尿や生ごみ、下水処理汚泥や余剰汚泥、消化汚泥、浄化槽汚泥、廃水や廃棄物の生物処理工程で生じる生物処理汚泥を脱水処理して得られる汚泥等が挙げられ、これらを複数含んでいても良い。これらの中で液体状や含水率が高い有機性廃棄物では、場外に排出する場合や再利用する場合に、作業効率が低下するため有機性廃棄物を改質する必要があり、本発明の改質方法が適用される。 The organic waste in the present invention mainly includes surplus and waste of animal feeds generated from livestock facilities such as pigs, chickens, cattle, sheep and horses, manure and garbage of domestic animals, sewage treatment sludge And surplus sludge, digested sludge, septic tank sludge, sludge obtained by dehydrating biological treatment sludge generated in the biological treatment process of wastewater and waste, and the like, and a plurality of these may be included. Among these organic wastes that are liquid or have a high water content, it is necessary to modify the organic waste because it reduces work efficiency when discharged out of the field or when reused. A reforming method is applied.
本発明におけるアルカリ剤は、消石灰(水酸化カルシウム)、苛性ソーダ、炭酸ソーダ、炭酸カリウム、水酸化カリウム等が挙げられる。これらの中から一種あるいは二種以上を組み合わせて使用することができる。本発明におけるアルカリ剤と水溶性高分子分散液の添加順序は同時、あるいはどちらを先に添加しても良いが、アルカリ剤を添加後に水溶性高分子分散液を添加する方が好ましい。アルカリ剤の添加率としては、対象とする有機性廃棄物によって変わってくるが、有機性廃棄物に対して、500〜10000ppmであり、1000〜8000ppmが好ましく適用できる範囲である。対象物のpHを中性から弱アルカリ域にすることにより処理効果が高まり、pH6〜11が好ましい範囲である。 Examples of the alkaline agent in the present invention include slaked lime (calcium hydroxide), caustic soda, sodium carbonate, potassium carbonate, potassium hydroxide and the like. One or a combination of two or more of these can be used. In the present invention, the alkali agent and the water-soluble polymer dispersion may be added at the same time or first, but it is preferable to add the water-soluble polymer dispersion after adding the alkali agent. The addition rate of the alkaline agent varies depending on the target organic waste, but is 500 to 10,000 ppm with respect to the organic waste, and is preferably in the range of 1000 to 8000 ppm. The treatment effect is enhanced by changing the pH of the object from neutral to weakly alkaline, and a pH of 6 to 11 is a preferred range.
本発明における水溶性高分子分散液は、塩水溶液中で、下記一般式(1)で表される単量体を必須として含有する単量体あるいは単量体混合物水溶液を、該塩水溶液中に可溶な高分子分散剤を共存させ、攪拌下、分散重合して得られる水溶性高分子分散液である。
一般式(1)
R1は水素又はメチル基、R2、R3は炭素数1〜3のアルキル基あるいはヒドロキシアルキル基、R4は炭素数1〜3のアルキルあるいはアルコキシル基、7〜20のアルキル基あるいはアリール基、Aは酸素またはNH、Bは炭素数2〜4のアルキレン基を表わす、X1 −は陰イオンをそれぞれ表わす。
The water-soluble polymer dispersion in the present invention contains a monomer or monomer mixture aqueous solution containing a monomer represented by the following general formula (1) as an essential component in a salt aqueous solution. It is a water-soluble polymer dispersion obtained by coexisting a soluble polymer dispersant and dispersion polymerization under stirring.
General formula (1)
R 1 is hydrogen or a methyl group, R 2 and R 3 are alkyl groups or hydroxyalkyl groups having 1 to 3 carbon atoms, R 4 is an alkyl or alkoxyl group having 1 to 3 carbon atoms, and an alkyl group or aryl group having 7 to 20 carbon atoms. , a is oxygen or NH, B represents an alkylene group having 2 to 4 carbon atoms, X 1 - represents respectively an anion.
本発明における水溶性高分子分散液を製造する際に使用する一般式(1)で表されるカチオン性単量体は、ジメチルアミノエチル(メタ)アクリレートやジメチルアミノプロピル(メタ)アクリルアミド等の塩化メチルや塩化ベンジルによる四級化物である。その例として一般式(1)で表わされるカチオン性単量体は、(メタ)アクリロイルオキシエチルトリメチルアンモニウム塩化物、(メタ)アクリロイルオキシ−2−ヒドロキシプロピルトリメチルアンモニウム塩化物、(メタ)アクリロイルアミノプロピルトリメチルアンモニウム塩化物、(メタ)アクリロイルオキシエチルジメチルベンジルアンモニウム塩化物、(メタ)アクリロイルオキシ−2−ヒドロキシプロピルジメチルベンジルアンモニウム塩化物、(メタ)アクリロイルアミノプロピルジメチルベンジルアンモニウム塩化物である。これらのカチオン性ビニル系単量体は一種を単独で用いることができ、二種以上を組み合わせて用いることもできる。一般式(1)で表されるカチオン性単量体は30〜100モル%の範囲が好ましい。これはカチオン度がこの範囲にあると分子量もある程度上げることができ、有機性廃棄物中の懸濁粒子のアニオン電荷を中和させる中和作用と、架橋吸着による凝集効果がバランス良く発揮できるためである。 The cationic monomer represented by the general formula (1) used for producing the water-soluble polymer dispersion in the present invention is a chloride such as dimethylaminoethyl (meth) acrylate or dimethylaminopropyl (meth) acrylamide. Quaternized product with methyl or benzyl chloride. Examples of the cationic monomer represented by the general formula (1) include (meth) acryloyloxyethyltrimethylammonium chloride, (meth) acryloyloxy-2-hydroxypropyltrimethylammonium chloride, and (meth) acryloylaminopropyl. Trimethylammonium chloride, (meth) acryloyloxyethyldimethylbenzylammonium chloride, (meth) acryloyloxy-2-hydroxypropyldimethylbenzylammonium chloride, (meth) acryloylaminopropyldimethylbenzylammonium chloride. These cationic vinyl monomers can be used alone or in combination of two or more. The cationic monomer represented by the general formula (1) is preferably in the range of 30 to 100 mol%. This is because when the cation degree is in this range, the molecular weight can be increased to some extent, and the neutralizing action for neutralizing the anionic charge of the suspended particles in the organic waste and the aggregation effect by cross-linking adsorption can be exhibited in a well-balanced manner. It is.
本発明における水溶性高分子分散液を製造する際に一般式(1)で表されるカチオン性単量体と非イオン性単量体を共重合させても良い。その場合に使用する非イオン性単量体としては、(メタ)アクリルアミド、N,N’−ジメチルアクリルアミド、アクリロニトリル、(メタ)アクリル酸−2−ヒドロキシエチル、ジアセトンアクリルアミド、N−ビニルピロリドン、N−ビニルホルムアミド、N−ビニルアセトアミド、アクリロイルモルホリン等が挙げられる。これらを二種以上組み合わせて使用しても良い。本発明における水溶性高分子分散液を構成するカチオン性単量体の総量は30〜100モル%が好ましい。 When producing the water-soluble polymer dispersion in the present invention, the cationic monomer represented by the general formula (1) and a nonionic monomer may be copolymerized. Nonionic monomers used in this case include (meth) acrylamide, N, N′-dimethylacrylamide, acrylonitrile, 2-hydroxyethyl (meth) acrylate, diacetone acrylamide, N-vinylpyrrolidone, N -Vinylformamide, N-vinylacetamide, acryloylmorpholine, etc. are mentioned. Two or more of these may be used in combination. As for the total amount of the cationic monomer which comprises the water-soluble polymer dispersion in this invention, 30-100 mol% is preferable.
本発明における水溶性高分子分散液は、イオン性が両性であっても良く、その場合は製造時に、下記一般式(2)で表されるアニオン性単量体が使用される。
一般式(2)
R5は水素、メチル基又はカルボキシメチル基、QはSO3 −、C6H4SO3 −、CONHC(CH3)2CH2SO3 −、C6H4COO−あるいはCOO−、R6は水素又はCOO−Y2 +、Y1あるいはY2は水素又は陽イオンをそれぞれ表わす。
The water-soluble polymer dispersion in the present invention may be amphoteric in ionicity. In that case, an anionic monomer represented by the following general formula (2) is used at the time of production.
General formula (2)
R 5 is hydrogen, methyl group or carboxymethyl group, Q is SO 3 − , C 6 H 4 SO 3 − , CONHC (CH 3 ) 2 CH 2 SO 3 − , C 6 H 4 COO − or COO − , R 6 represent respectively + Y 2, Y 1 or Y 2 is hydrogen or a cation and - is hydrogen or COO.
本発明における両性水溶性高分子分散液を製造する際に使用する前記一般式(2)で表されるアニオン性単量体は0〜15モル%の範囲である。15モル%を超えると有機性廃棄物中の懸濁粒子のアニオン電荷を中和させる中和作用が低下するので好ましくはない。アニオン性単量体の例としては、ビニルスルホン酸、ビニルベンゼンスルホン酸あるいは2−アクリルアミド−2−メチルプロパンスルホン酸、メタクリル酸、アクリル酸、イタコン酸、マレイン酸、フタル酸あるいはp−カルボキシスチレン酸等が挙げられる。これらを二種以上組み合わせて使用しても良い。又、一般式(1)で表されるカチオン性単量体と一般式(2)で表されるアニオン性単量体を使用しても良く、一般式(1)で表されるカチオン性単量体と一般式(2)で表されるアニオン性単量体と前記非イオン性単量体を使用しても良い。 The anionic monomer represented by the general formula (2) used in producing the amphoteric water-soluble polymer dispersion in the present invention is in the range of 0 to 15 mol%. If it exceeds 15 mol%, the neutralizing action for neutralizing the anionic charge of the suspended particles in the organic waste is reduced, which is not preferable. Examples of anionic monomers include vinyl sulfonic acid, vinyl benzene sulfonic acid or 2-acrylamido-2-methylpropane sulfonic acid, methacrylic acid, acrylic acid, itaconic acid, maleic acid, phthalic acid or p-carboxystyrene acid Etc. Two or more of these may be used in combination. Further, a cationic monomer represented by the general formula (1) and an anionic monomer represented by the general formula (2) may be used, and the cationic monomer represented by the general formula (1) may be used. You may use a monomer, the anionic monomer represented by General formula (2), and the said nonionic monomer.
本発明における水溶性高分子分散液は塩水中分散重合法によって製造する。製造方法は、特開昭61−123610号公報、特開62−20511号公報、特開2007−16086号公報、特開2016−003255号公報等によって開示されている公知の方法による。即ち、塩水溶液中において、分散剤として該塩水溶液中に溶解可能な水溶性高分子を共存させイオン性単量体及び非イオン性単量体混合物を分散重合して製造する。その場合、重合遅延性物質を全単量体に対し0.5〜5モル%添加することにより、増粘が抑制可能であり、重量平均分子量が高い水溶性重合体を製造することができる。又、前記重合遅延性物質はイタコン酸、マレイン酸、フタル酸、アリルアミンおよびジアリルジメチルアンモニウムクロライドから選択される一種以上である。 The water-soluble polymer dispersion in the present invention is produced by a salt water dispersion polymerization method. The manufacturing method is a known method disclosed in Japanese Patent Application Laid-Open No. 61-123610, Japanese Patent Application Laid-Open No. 62-20511, Japanese Patent Application Laid-Open No. 2007-16086, Japanese Patent Application Laid-Open No. 2006-003255, and the like. That is, it is produced by dispersing and polymerizing an ionic monomer and nonionic monomer mixture in the aqueous salt solution in the presence of a water-soluble polymer that can be dissolved in the aqueous salt solution as a dispersant. In that case, by adding 0.5 to 5 mol% of a polymerization retarding substance with respect to all monomers, it is possible to produce a water-soluble polymer that can suppress thickening and has a high weight average molecular weight. The polymerization retarding substance is at least one selected from itaconic acid, maleic acid, phthalic acid, allylamine, and diallyldimethylammonium chloride.
塩水中分散重合時の重合条件は通常、使用する単量体や共重合モル%によって適宜決定し、温度としては0〜100℃の範囲で行う。重合開始はラジカル重合開始剤を使用する。これら開始剤は油溶性あるいは水溶性のどちらでも良く、アゾ系、過酸化物系、レドックス系の何れでも重合することが可能である。油溶性アゾ系開始剤の例としては、2、2’−アゾビスイソブチロニトリル、1、1’−アゾビス(シクロヘキサンカルボニトリル)、2、2’−アゾビス(2−メチルブチロニトリル)、2、2’−アゾビス(2−メチルプロピオネート)、4、4’−アゾビス(4−メトキシ−2、4−ジメチル)バレロニトリル等が挙げられ、水混溶性溶剤に溶解し添加する。 The polymerization conditions at the time of dispersion polymerization in brine are usually determined appropriately depending on the monomers used and the copolymerization mol%, and the temperature is in the range of 0 to 100 ° C. For the initiation of polymerization, a radical polymerization initiator is used. These initiators may be either oil-soluble or water-soluble, and can be polymerized by any of azo, peroxide, and redox systems. Examples of oil-soluble azo initiators are 2,2′-azobisisobutyronitrile, 1,1′-azobis (cyclohexanecarbonitrile), 2,2′-azobis (2-methylbutyronitrile), 2,2′-azobis (2-methylpropionate), 4,4′-azobis (4-methoxy-2,4-dimethyl) valeronitrile, and the like are mentioned, which are dissolved in a water-miscible solvent and added.
水溶性アゾ系開始剤の例としては、2、2’−アゾビス(2−アミジノプロパン)二塩酸塩、2、2’−アゾビス〔2−(2−イミダゾリン−2−イル)プロパン〕二塩酸塩、4、4’−アゾビス(4−シアノ吉草酸)等が挙げられる。又、レドックス系の例としては、ペルオキソ二硫酸アンモニウムと亜硫酸ナトリウム、亜硫酸水素ナトリウム、トリメチルアミン、テトラメチルエチレンジアミン等との組み合わせが挙げられる。更に過酸化物の例としては、ペルオキソ二硫酸アンモニウム或いはカリウム、過酸化水素、ベンゾイルペルオキサイド、ラウロイルペルオキサイド、オクタノイルペルオキサイド、サクシニックペルオキサイド、t−ブチルペルオキシ2−エチルヘキサノエート等を挙げることができる。これら開始剤の中で最も好ましいのは、水溶性アゾ開始剤の2、2’−アゾビス(2−アミジノプロパン)二塩酸塩、2、2’−アゾビス〔2−(2−イミダゾリン−2−イル)プロパン〕二塩酸塩である。アゾ系開始剤の添加率は、重合開始時、単量体当たり50〜500ppm、好ましくは70〜200ppm添加する。しかし、一回の添加では重合率が低くなるので、数回に分けて添加することが好ましい。 Examples of water-soluble azo initiators include 2,2′-azobis (2-amidinopropane) dihydrochloride, 2,2′-azobis [2- (2-imidazolin-2-yl) propane] dihydrochloride 4,4′-azobis (4-cyanovaleric acid) and the like. Examples of redox systems include a combination of ammonium peroxodisulfate and sodium sulfite, sodium hydrogen sulfite, trimethylamine, tetramethylethylenediamine and the like. Examples of peroxides include ammonium or potassium peroxodisulfate, hydrogen peroxide, benzoyl peroxide, lauroyl peroxide, octanoyl peroxide, succinic peroxide, t-butylperoxy 2-ethylhexanoate, and the like. be able to. Most preferred among these initiators are 2,2′-azobis (2-amidinopropane) dihydrochloride, 2,2′-azobis [2- (2-imidazolin-2-yl), a water-soluble azo initiator. ) Propane] dihydrochloride. The addition rate of the azo initiator is 50 to 500 ppm, preferably 70 to 200 ppm per monomer at the start of polymerization. However, since the polymerization rate is lowered by a single addition, it is preferable to add in several portions.
又、レドックス系開始剤で共重合する場合、40℃以上の条件で重合を開始させると重合の制御は難しく、急激な温度上昇や重合液の塊状化などが起きて、高重合度で安定な分散液が得られないため、15〜35℃が好ましい。この開始剤の添加率は、重合開始時、単量体当たり5〜100ppm、好ましくは10〜50ppm添加する。しかし、一回の添加では重合率が低くなるので、数回添加することが好ましい。添加回数としては、2〜5回、好ましくは2〜3回である。これらイオン性高分子からなる高分子分散剤の添加率としては、対単量体1〜30質量%であり、好ましくは2〜20質量%である。1質量%以下では、分散剤としての効果がなく、30質量%以上では、分散液の粘性が高くなる上、コスト的に不利になる。 In addition, when copolymerizing with a redox initiator, it is difficult to control the polymerization when the polymerization is started at a temperature of 40 ° C. or more, and a rapid temperature rise or agglomeration of the polymerization solution occurs, resulting in a high degree of polymerization and stability. Since a dispersion liquid cannot be obtained, 15-35 degreeC is preferable. The initiator is added at a rate of 5 to 100 ppm, preferably 10 to 50 ppm per monomer at the start of polymerization. However, since the polymerization rate is lowered by a single addition, it is preferably added several times. As addition frequency, it is 2-5 times, Preferably it is 2-3 times. The addition rate of the polymer dispersant composed of these ionic polymers is 1 to 30% by mass, preferably 2 to 20% by mass with respect to the monomer. If it is 1% by mass or less, there is no effect as a dispersing agent, and if it is 30% by mass or more, the viscosity of the dispersion becomes high and the cost becomes disadvantageous.
本発明における水溶性高分子分散液を製造する際の重合時あるいは重合後、構造変性剤として架橋性単量体を使用しても良い。使用する場合は、架橋性単量体を単量体総量に対し、0.00005〜0.050質量%の範囲内で存在させる。単量体組成や重合条件により異なるが、0.050質量%を超えると架橋が進行しすぎて水不溶性となるため本発明の用途としては好ましくはない。架橋性単量体の例としては、N,N’−メチレンビス(メタ)アクリルアミド、トリアリルアミン、ジメタクリル酸エチレングリコール、ジメタクリル酸ジエチレングリコール、ジメタクリル酸トリエチレングリコール、ジメタクリル酸テトラエチレングリコール、ジメタクリル酸−1,3−ブチレングリコール、ジ(メタ)アクリル酸ポリエチレングリコール、N−ビニル(メタ)アクリルアミド、N−メチルアリルアクリルアミド、アクリル酸グリシジル、ポリエチレングリコールジグリシジルエーテル、アクロレイン、グリオキザール、ビニルトリメトキシシラン等が挙げられ、N,N’−メチレンビス(メタ)アクリルアミドが好ましく適用されている。 A crosslinkable monomer may be used as a structural modifier during or after the polymerization for producing the water-soluble polymer dispersion in the present invention. When used, the crosslinkable monomer is present in the range of 0.00005 to 0.050 mass% with respect to the total amount of monomers. Although it varies depending on the monomer composition and polymerization conditions, if it exceeds 0.050 mass%, crosslinking proceeds excessively and becomes insoluble in water, which is not preferable for use in the present invention. Examples of the crosslinkable monomer include N, N′-methylenebis (meth) acrylamide, triallylamine, ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate, tetraethylene glycol dimethacrylate, Methacrylic acid-1,3-butylene glycol, polyethylene glycol di (meth) acrylate, N-vinyl (meth) acrylamide, N-methylallylacrylamide, glycidyl acrylate, polyethylene glycol diglycidyl ether, acrolein, glyoxal, vinyltrimethoxy Silane and the like can be mentioned, and N, N′-methylenebis (meth) acrylamide is preferably applied.
本発明における水溶性高分子分散液を製造する際に使用する高分子分散剤は、イオン性、非イオン性とも使用可能であるが、好ましくはイオン性、さらに好ましくはカチオン性である。カチオン性高分子分散剤の場合、(メタ)アクリロイルオキシエチルトリメチルアンモニウム塩化物やジメチルジアリルアンモニウム塩化物などのカチオン性単量体の(共)重合体を高分子分散剤として使用するが、カチオン性単量体と非イオン性単量体との共重合体も使用可能である。非イオン性単量体の例としては、アクリルアミド、N−ビニルホルムアミド、N−ビニルアセトアミド、N−ビニルピロリドン、N、N−ジメチルアクリルアミド、アクリロニトリル、ジアセトンアクリルアミド、2−ヒドロキシエチル(メタ)アクリレート等であるが、アクリルアミドとの共重合体が好ましい。 The polymer dispersant used in the production of the water-soluble polymer dispersion in the present invention can be either ionic or nonionic, but is preferably ionic, and more preferably cationic. In the case of a cationic polymer dispersant, a (co) polymer of a cationic monomer such as (meth) acryloyloxyethyltrimethylammonium chloride or dimethyldiallylammonium chloride is used as the polymer dispersant. Copolymers of monomers and nonionic monomers can also be used. Examples of nonionic monomers include acrylamide, N-vinylformamide, N-vinylacetamide, N-vinylpyrrolidone, N, N-dimethylacrylamide, acrylonitrile, diacetone acrylamide, 2-hydroxyethyl (meth) acrylate, etc. However, a copolymer with acrylamide is preferred.
また、非イオン性高分子分散剤としては、ポリビニルピロリドン、アクリルアミド/ポリビニルカプロラクタム共重合体、アクリルアミド/スチレン共重合体、無水マレイン酸/ブテン共重物の完全アミド化物などアミド基と若干の疎水性基を有する水溶性重合体も有効である。 Nonionic polymer dispersants include polyvinylpyrrolidone, acrylamide / polyvinylcaprolactam copolymer, acrylamide / styrene copolymer, and complete amidation product of maleic anhydride / butene copolymer, and some hydrophobicity A water-soluble polymer having a group is also effective.
これらカチオン性高分子分散剤の分子量としては、5,000〜200万、好ましくは5万〜100万である。また、非イオン性高分子分散剤の分子量としては、1,000〜10万、好ましくは1,000〜5万である。これら非イオン性あるいはイオン性高分子分散剤の添加率は、単量体に対して1〜20質量%であり、好ましくは5〜15質量%である。 The molecular weight of these cationic polymer dispersants is 5,000 to 2,000,000, preferably 50,000 to 1,000,000. The molecular weight of the nonionic polymer dispersant is 1,000 to 100,000, preferably 1,000 to 50,000. The addition rate of these nonionic or ionic polymer dispersants is 1 to 20% by mass, preferably 5 to 15% by mass, based on the monomer.
使用する塩類としては、ナトリウムやカリウムのようなアルカリ金属イオンやアンモニウムイオンなどの陽イオンとハロゲン化物イオン、硫酸イオン、硝酸イオン、リン酸イオンなどの陰イオンとを組み合わせた塩が使用可能であるが、多価陰イオンとの塩がより好ましい。これら塩類の塩濃度としては、10質量%〜飽和濃度まで使用できる。 As the salt to be used, a combination of a cation such as an alkali metal ion such as sodium or potassium or an ammonium ion and an anion such as halide ion, sulfate ion, nitrate ion or phosphate ion can be used. However, a salt with a polyvalent anion is more preferable. The salt concentration of these salts can be used from 10% by mass to the saturated concentration.
重合濃度としては、単量体濃度として10質量%〜35質量%であるが、好ましくは15質量%〜30質量%である。これは単量体濃度が高い程、輸送コストの問題で経済的に有利であるが、単量体濃度が35質量%を超えると製造時に増粘が大きくなり分散液が得られ難くなるためである。単量体供給方法としては、重合開始時、一括して仕込んでも良いし、適宜分割して仕込んでも良い。 The polymerization concentration is 10% by mass to 35% by mass as the monomer concentration, and preferably 15% by mass to 30% by mass. This is because the higher the monomer concentration, the more economically advantageous due to the problem of transportation costs. However, if the monomer concentration exceeds 35% by mass, the viscosity increases during production and it becomes difficult to obtain a dispersion. is there. As a monomer supply method, it may be charged all at once at the start of polymerization, or may be charged in an appropriate manner.
本発明における水溶性高分子分散液の高分子濃度が0.2質量%になるように水で完全溶解したときの25℃において測定した粘度が、100mPa・s以下の範囲である。70mPa・s以下がより好ましく、50mPa・s以下がより一層好ましい。水溶性高分子分散液がこの範囲の粘度物性を有すると有機性廃棄物に添加時に分散性が良く効率的に混合される。0.2質量%水溶液粘度は、B型粘度計において2号ローター、30rpmで測定した値である。B型粘度計としては東京計器製B8M等が使用される。 The viscosity measured at 25 ° C. when completely dissolved in water so that the polymer concentration of the water-soluble polymer dispersion in the present invention is 0.2% by mass is in the range of 100 mPa · s or less. 70 mPa · s or less is more preferable, and 50 mPa · s or less is even more preferable. When the water-soluble polymer dispersion has viscosity properties in this range, it is efficiently mixed with organic waste when dispersed. The 0.2 mass% aqueous solution viscosity is a value measured with a No. 2 rotor and 30 rpm in a B-type viscometer. As the B-type viscometer, B8M manufactured by Tokyo Keiki Co., Ltd. is used.
本発明における水溶性高分子分散液の分子量は重量平均分子量で100万〜1000万であり、好ましくは100万〜800万である。又、水溶性高分子分散液を2質量%硫酸アンモニウム水中に高分子濃度が0.5質量%になるように完全溶解したときの25℃において回転粘度計にて測定した塩水溶液粘度は、5mPa・s以上、100mPa・s以下の範囲であり、好ましくは5mPa・s以上、70mPa・s以下である。この範囲の粘度物性を有すると凝集処理効果が最適となる。この0.5質量%塩水溶液粘度は、B型粘度計において1号ローター、60rpmで測定した値である。 The molecular weight of the water-soluble polymer dispersion in the present invention is 1 million to 10 million, preferably 1 million to 8 million, in terms of weight average molecular weight. Further, when the water-soluble polymer dispersion was completely dissolved in 2% by mass ammonium sulfate water so that the polymer concentration was 0.5% by mass, the salt aqueous solution viscosity measured at 25 ° C. with a rotational viscometer was 5 mPa · The range is from s to 100 mPa · s, preferably from 5 mPa · s to 70 mPa · s. When the viscosity physical properties are within this range, the effect of the coagulation treatment is optimal. This 0.5 mass% salt aqueous solution viscosity is a value measured with a No. 1 rotor and 60 rpm in a B-type viscometer.
本発明における水溶性高分子分散液は、アルカリ剤と併用して有機性廃棄物に添加、混合し凝集させることで、有機性廃棄物を改質する方法である。有機性廃棄物は主に豚、鶏、牛、羊、馬等の家畜の畜産施設から発生する動物用の飼料の余剰や廃棄分、飼育動物の糞尿や生ごみ、下水処理汚泥や余剰汚泥、消化汚泥、浄化槽汚泥、廃水や廃棄物の生物処理工程で生じる生物処理汚泥を脱水処理して得られる汚泥等が挙げられる。有機性廃棄物の指標となる有機物量VSS値(浮遊物質中の強熱減量、質量%対SS)が、80質量%/SS以上が好ましく、85質量%/SS以上がより好ましく適用される。含水率は70質量%以上から90質量%以下の範囲が好ましい。SS濃度では10質量%以上から30質量%以下が好ましく適用される。尚、各種測定値は、定法(下水試験方法)に基づく測定による。 The water-soluble polymer dispersion in the present invention is a method for modifying an organic waste by adding it to an organic waste in combination with an alkaline agent, mixing it and aggregating it. Organic waste mainly includes surplus and waste of animal feed generated from livestock facilities such as pigs, chickens, cattle, sheep and horses, animal waste and waste, sewage treatment sludge and surplus sludge, Examples include digested sludge, septic tank sludge, and sludge obtained by dehydrating biologically treated sludge generated in the biological treatment process of wastewater and waste. The organic matter VSS value (ignition loss in suspended matter, mass% vs. SS) serving as an index of organic waste is preferably 80% by mass / SS or more, more preferably 85% by mass / SS or more. The moisture content is preferably in the range of 70% by mass to 90% by mass. The SS concentration is preferably 10% by mass to 30% by mass. Various measured values are based on measurements based on a conventional method (sewage test method).
有機性廃棄物の中でも特に動物用の液体状の飼料を廃棄物として排出する場合や、粉末状の飼料と混合して再利用する場合が生じる。排出する場合、作業効率が低下したり、流動性があると粉末状の飼料と混合し難かったり、腐りやすくなり長時間の保存ができなくなったりするため液体状の飼料を改質、固化処理する必要がある。又、液体状や含水率が高い場合では体積が大きく保管場所の問題等が生じる。この様な場合において本発明における改質方法が好適である。本発明における改質方法が動物用の液体状の飼料に好適な理由としては、アルカリ剤の添加によって、飼料中の懸濁粒子のアニオン電荷度を高めること、飼料中に含有される澱粉の粘性を低下させること、乳酸発酵により生成した乳酸を乳酸塩に変換すること等が生じ、水溶性高分子分散液の効果が最大限に発揮されることが推測される。 Among organic wastes, there are cases where liquid feed for animals is discharged as waste, or mixed with powdered feed for reuse. When discharging, the liquid feed is modified and solidified because work efficiency decreases or fluidity makes it difficult to mix with powdered feed, or it tends to rot and cannot be stored for a long time. There is a need. Further, when the liquid state or the water content is high, the volume is large and the problem of the storage place arises. In such a case, the reforming method of the present invention is suitable. The reason why the modification method of the present invention is suitable for animal liquid feeds is to increase the anionic charge of suspended particles in the feed by adding an alkaline agent, and to increase the viscosity of the starch contained in the feed. It is presumed that the effect of the water-soluble polymer dispersion is exhibited to the maximum by reducing the lactic acid and converting lactic acid produced by lactic acid fermentation into lactate.
本発明における水溶性高分子分散液は、溶解性が優れるため製品のままの状態で添加することもできるし、任意の濃度に水で溶解、希釈して有機性廃棄物に添加できる。溶解する場合は、一般的に溶解濃度0.05〜0.3質量%を適用する。又、有機性廃棄物に対する添加率は、通常50〜2000ppmであるが、対象とする有機性廃棄物により任意に調節する。アルカリ剤の他に塩化第二鉄、ポリ硫酸第二鉄、ポリ塩化アルミニウム、硫酸バンド等の無機系凝集剤と併用しても差し支えない。 Since the water-soluble polymer dispersion in the present invention has excellent solubility, it can be added as it is, or can be added to organic waste after being dissolved and diluted with water to an arbitrary concentration. In the case of dissolution, a dissolution concentration of 0.05 to 0.3% by mass is generally applied. Moreover, although the addition rate with respect to organic waste is 50-2000 ppm normally, it adjusts arbitrarily with the organic waste made into object. In addition to the alkali agent, it may be used in combination with an inorganic flocculant such as ferric chloride, polyferric sulfate, polyaluminum chloride, and sulfuric acid band.
本発明におけるアルカリ剤及び水溶性高分子分散液を添加処理後、有機性廃棄物を汚泥脱水で使用される様な圧搾機、例えば、スクリュー濃縮機、遠心濃縮機、楕円盤型濃縮機等や、ベルトプレス、遠心脱水機、スクリュープレス、多重円盤型脱水機、ロータリープレス、フィルタープレス等の脱水機を任意に適用できる。これらの他にも圧搾に関して同様な技術思想を任意に適用できる。 After the addition treatment of the alkaline agent and the water-soluble polymer dispersion in the present invention, the organic waste is used in a sludge dewatering machine such as a screw concentrator, a centrifugal concentrator, an elliptical concentrator, etc. A dehydrator such as a belt press, a centrifugal dehydrator, a screw press, a multiple disk dehydrator, a rotary press, a filter press, etc. can be arbitrarily applied. In addition to these, the same technical idea regarding compression can be arbitrarily applied.
以下、実施例によって本発明を更に詳しく説明するが、本発明はその要旨を超えない限り、以下の実施例に制約されるものではない。 EXAMPLES Hereinafter, although an Example demonstrates this invention in more detail, this invention is not restrict | limited to a following example, unless the summary is exceeded.
先ず、本発明で使用する水溶性高分子分散液試料A〜Cを常法により製造した。これらの組成、物性を表1に示す。又、高分子凝集剤と汎用されている試料1〜5を準備、調製した。これらの組成、物性を表1に示す。更に汎用品の凝結剤試料6(ジアリルジメチルアンモニウムクロリド共重合体、pH7でのカチオン当量6.1meq/g、製品濃度35%、重量平均分子量25万)、凝集剤試料7(ポリアミジン系水溶性高分子、pH7でのカチオン当量5.2meq/g、粉末品、重量平均分子量300万)も用意した。 First, water-soluble polymer dispersion samples A to C used in the present invention were produced by a conventional method. These compositions and physical properties are shown in Table 1. In addition, samples 1 to 5 which are generally used as a polymer flocculant were prepared and prepared. These compositions and physical properties are shown in Table 1. Furthermore, a general-purpose coagulant sample 6 (diallyldimethylammonium chloride copolymer, cation equivalent 6.1 meq / g at pH 7, product concentration 35%, weight average molecular weight 250,000), flocculant sample 7 (polyamidine water-soluble high Molecule, cation equivalent of 5.2 meq / g at pH 7, powder product, weight average molecular weight 3 million).
(表1)
DMQ:アクリロイルオキシエチルトリメチルアンモニウム塩化物
DMC:メタクリロイルオキシエチルトリメチルアンモニウム塩化物
DMBZ:アクリロイルオキシエチルジメチルベンジルアンモニウム塩化物
AAM:アクリルアミド
AAC:アクリル酸
形態;DR:塩水液中分散重合液、EM:油中水型エマルジョン、P:粉末
0.2質量%水溶液粘度;高分子濃度が0.2質量%になるように水で溶解したときの25℃において測定した粘度(mPa・s)
0.5質量%塩水溶液粘度(塩水中分散重合体):2質量%硫酸アンモニウム水中に高分子濃度が0.5質量%になるように溶解したときの25℃において測定した粘度(mPa・s)。
0.5質量%塩水溶液粘度(塩水中分散重合体以外);4質量%食塩水中に高分子濃度が0.5質量%になるように溶解したときの25℃において測定した粘度(mPa・s)。
(Table 1)
DMQ: acryloyloxyethyltrimethylammonium chloride DMC: methacryloyloxyethyltrimethylammonium chloride DMBZ: acryloyloxyethyldimethylbenzylammonium chloride AAM: acrylamide AAC: acrylic acid form; DR: dispersion polymer solution in brine, EM: oil Water-type emulsion, P: 0.2 mass% powder aqueous solution viscosity; viscosity measured at 25 ° C. when dissolved in water so that the polymer concentration is 0.2 mass% (mPa · s)
0.5% by weight salt aqueous solution viscosity (dispersed polymer in salt water): Viscosity measured at 25 ° C. when dissolved in 2% by weight ammonium sulfate water so that the polymer concentration is 0.5% by weight (mPa · s) .
Viscosity measured at 25 ° C. (mPa · s) when dissolved in 4% by weight salt solution so that the polymer concentration is 0.5% by weight. ).
(実施例1)
本発明におけるアルカリ剤及び水溶性高分子分散液添加処方の改質処理性能を評価した。対象の有機性廃棄物として、某養豚場の養豚向け液体状飼料の廃棄分を主成分とするスラリーを用いた。当該廃棄物試料の分析値は下記の様であった。pH3.7、EC756mS/m、SS濃度16.4質量%、TS濃度18.7質量%、VSS87.2質量%/SS、アニオン量2.35meq/L。当該廃棄物試料をメスシリンダーに100mL採取し試験に用いた。一液目にアルカリ剤として消石灰を対液4500ppm添加後、二液目として表1の本発明における水溶性高分子分散液試料Aの0.2質量%溶解液を、対液400ppm添加、スパチュラによる混合攪拌100回実施後、ナイロン製濾布(#202)により濾過し、60秒後の濾液量、フロック径を測定した。測定後、60秒間濾過した汚泥をプレス圧3Kg/cm2で30秒間脱水し、ケーキ含水率(105℃で20時間乾燥)を測定した。その結果を表2に示す。尚、消石灰添加後の廃棄物試料のpHは7.0であった。
Example 1
The reforming performance of the alkali agent and water-soluble polymer dispersion addition formulation in the present invention was evaluated. As the target organic waste, a slurry mainly composed of a liquid feed waste for pig farming in a pig farm was used. The analysis value of the waste sample was as follows. pH 3.7, EC 756 mS / m, SS concentration 16.4% by mass, TS concentration 18.7% by mass, VSS 87.2% by mass / SS, anion amount 2.35 meq / L. 100 mL of the waste sample was collected in a graduated cylinder and used for the test. After adding 4500 ppm of slaked lime as an alkaline agent to the first liquid, add 0.2 ppm by weight of the water-soluble polymer dispersion sample A in Table 1 of the present invention in Table 1 as the second liquid, add 400 ppm to the liquid, and with a spatula After 100 times of mixing and stirring, the mixture was filtered through a nylon filter cloth (# 202), and the filtrate amount and floc diameter after 60 seconds were measured. After the measurement, the sludge filtered for 60 seconds was dehydrated at a press pressure of 3 kg / cm 2 for 30 seconds, and the moisture content of the cake (dried at 105 ° C. for 20 hours) was measured. The results are shown in Table 2. The waste sample after addition of slaked lime had a pH of 7.0.
(実施例2〜8)
実施例1と同じ廃棄物試料を用い、同様な試験を実施した。一液目に消石灰あるいは苛性ソーダを添加、二液目に表1の本発明における水溶性高分子分散液試料A〜Cを添加し試験を実施した。その結果を表2に示す。
(Examples 2 to 8)
A similar test was carried out using the same waste sample as in Example 1. The test was carried out by adding slaked lime or caustic soda to the first liquid and adding the water-soluble polymer dispersion samples A to C of the present invention in Table 1 to the second liquid. The results are shown in Table 2.
(比較例1〜14)
比較試験として実施例1と同じ廃棄物試料を用い、同様な試験を実施した。その結果を表2に示す。
(Comparative Examples 1-14)
As a comparative test, the same waste test as in Example 1 was used, and a similar test was performed. The results are shown in Table 2.
(表2)
(Table 2)
本発明におけるアルカリ剤及び水溶性高分子分散液試料を添加時、廃棄物試料はフロックを形成し、濾過速度が速く凝集性能が高く、ケーキ含水率も低下を示した。本発明におけるアルカリ剤及び水溶性高分子分散液を添加することで有機性廃棄物を効率良く改質することが確認できた。一方、本発明における水溶性高分子分散液以外のポリマーを使用した場合や、アルカリ剤を使用しない場合では、フロックを殆ど形成せず、有機性廃棄物の改質は認められなかった。
When the alkaline agent and the water-soluble polymer dispersion sample in the present invention were added, the waste sample formed flocs, the filtration rate was high, the aggregation performance was high, and the cake moisture content was also reduced. It was confirmed that the organic waste was efficiently modified by adding the alkaline agent and the water-soluble polymer dispersion in the present invention. On the other hand, when a polymer other than the water-soluble polymer dispersion in the present invention was used or when an alkaline agent was not used, almost no floc was formed, and no modification of organic waste was observed.
Claims (4)
一般式(1)
R1は水素又はメチル基、R2、R3は炭素数1〜3のアルキル基あるいはヒドロキシアルキル基、R4は炭素数1〜3のアルキルあるいはアルコキシル基、7〜20のアルキル基あるいはアリール基、Aは酸素またはNH、Bは炭素数2〜4のアルキレン基を表わす、X1 −は陰イオンをそれぞれ表わす。 A water-soluble polymer that is soluble in an aqueous salt solution as a dispersant containing a monomer or a monomer mixture containing an alkaline agent and a monomer represented by the following general formula (1) as an essential component in organic waste A method for reforming organic waste, comprising adding and mixing a water-soluble polymer dispersion obtained by dispersion polymerization under stirring in an aqueous salt solution.
General formula (1)
R 1 is hydrogen or a methyl group, R 2 and R 3 are alkyl groups or hydroxyalkyl groups having 1 to 3 carbon atoms, R 4 is an alkyl or alkoxyl group having 1 to 3 carbon atoms, and an alkyl group or aryl group having 7 to 20 carbon atoms. , a is oxygen or NH, B represents an alkylene group having 2 to 4 carbon atoms, X 1 - represents respectively an anion.
2. The organic waste reforming method according to claim 1, wherein an organic matter amount VSS value of the organic waste is 80 mass% / SS or more.
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