JP5058934B2 - Method for regenerating waste cooking oil and cutting oil obtained thereby - Google Patents
Method for regenerating waste cooking oil and cutting oil obtained thereby Download PDFInfo
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- JP5058934B2 JP5058934B2 JP2008259211A JP2008259211A JP5058934B2 JP 5058934 B2 JP5058934 B2 JP 5058934B2 JP 2008259211 A JP2008259211 A JP 2008259211A JP 2008259211 A JP2008259211 A JP 2008259211A JP 5058934 B2 JP5058934 B2 JP 5058934B2
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- 239000002699 waste material Substances 0.000 title claims description 35
- 238000000034 method Methods 0.000 title claims description 26
- 239000008162 cooking oil Substances 0.000 title claims description 13
- 239000010730 cutting oil Substances 0.000 title claims description 12
- 230000001172 regenerating effect Effects 0.000 title description 3
- 239000003921 oil Substances 0.000 claims description 72
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 31
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 30
- 239000008157 edible vegetable oil Substances 0.000 claims description 26
- 239000007788 liquid Substances 0.000 claims description 17
- 238000000926 separation method Methods 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 239000012071 phase Substances 0.000 claims description 12
- 238000003756 stirring Methods 0.000 claims description 10
- 238000005886 esterification reaction Methods 0.000 claims description 8
- 230000032050 esterification Effects 0.000 claims description 7
- 238000005498 polishing Methods 0.000 claims description 7
- 238000001914 filtration Methods 0.000 claims description 6
- 230000005484 gravity Effects 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- 238000005273 aeration Methods 0.000 claims description 5
- 239000003518 caustics Substances 0.000 claims description 5
- 239000004927 clay Substances 0.000 claims description 5
- 238000004140 cleaning Methods 0.000 claims description 5
- 239000010710 diesel engine oil Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 229920002472 Starch Polymers 0.000 claims description 4
- 229910021536 Zeolite Inorganic materials 0.000 claims description 4
- 239000003463 adsorbent Substances 0.000 claims description 4
- 239000008346 aqueous phase Substances 0.000 claims description 4
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 230000000149 penetrating effect Effects 0.000 claims description 4
- 235000019698 starch Nutrition 0.000 claims description 4
- 239000008107 starch Substances 0.000 claims description 4
- 239000010457 zeolite Substances 0.000 claims description 4
- 238000001179 sorption measurement Methods 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 2
- 238000011069 regeneration method Methods 0.000 claims description 2
- 230000008929 regeneration Effects 0.000 claims 1
- 230000003068 static effect Effects 0.000 claims 1
- 235000019198 oils Nutrition 0.000 description 59
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 15
- 238000005520 cutting process Methods 0.000 description 8
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000012535 impurity Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 4
- 239000010685 fatty oil Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 239000010705 motor oil Substances 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 206010016322 Feeling abnormal Diseases 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- -1 fatty acid ester Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000010794 food waste Substances 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 239000010813 municipal solid waste Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/74—Recovery of fats, fatty oils, fatty acids or other fatty substances, e.g. lanolin or waxes
Landscapes
- Detergent Compositions (AREA)
- Fats And Perfumes (AREA)
- Lubricants (AREA)
Description
本発明は、廃食用油、特に使用済みてんぷら油の再生方法及び得られた再生油を利用した切削油等に関する。 The present invention relates to a method for regenerating waste edible oil, particularly used tempura oil, and cutting oil using the obtained regenerated oil.
外食産業加工工場、飲食店、一般家庭などからてんぷら等に使用した使用済みの食用油が生じ、年々その量が増大し処分に困難を来たしている。この廃食用油は、土中に埋めたり、下水に流したりすると水圏を汚染する環境問題を引き起こすことになる。
廃食用油を処分する方法として、紙廃材等を加工した油吸収材に吸収させて廃棄する方法や高分子ゲル化剤を加えて固形化して生ごみとともに廃棄する方法などが一般に行われている。しかし、大量処理となると、吸収された油がしみだしたり、一度固化したものが液状化して流れ出すなどの不都合があった。
また、脂肪酸とグリセリンのエステルからなる大豆油、コーン油、ゴマ油、紅花油、オリーブ油等の食用油(特にてんぷら油)は、いおうを含有しないことから、使用済み後にエネルギー源として注目されている。
Used cooking oils used for tempura etc. are generated from processing factories in restaurants, restaurants, general households, etc., and the amount increases year by year, making disposal difficult. If this waste cooking oil is buried in the soil or poured into sewage, it will cause environmental problems that pollute the hydrosphere.
As a method of disposing of waste cooking oil, a method of absorbing and discarding paper waste materials etc. in a processed oil absorbent material, a method of adding a polymer gelling agent to solidify and disposing it with garbage, etc. are generally performed . However, in the case of mass treatment, there are inconveniences such as absorbed oil oozing out and once solidified, it liquefies and flows out.
In addition, edible oils (especially tempura oil) such as soybean oil, corn oil, sesame oil, safflower oil, olive oil and the like, which are esters of fatty acids and glycerin, are notable as an energy source after being used because they do not contain sulfur.
そして、廃食用油から不純物を除去後、廃食用油と水とを接触し、油中に含まれる水溶性物質を除き、続いてオゾン、酸素又は空気を含ませて酸化活性化し、燃料とする方法(例えば、特許文献1参照)や、廃食用油とアルコールを水酸化カルシウム又は酸化カルシウムの固体触媒の存在下で反応させ、脂肪酸エステルを含む燃料を製造する方法(例えば、特許文献2参照)などが提案されている。
ところが、コスト及びその望まれる基準値を達成する手段についていまだ解決されていないため、鉱油系燃料の一部としてでも代替することができていないようである。
And after removing impurities from waste edible oil, contact the waste edible oil and water, remove water-soluble substances contained in the oil, and subsequently oxidize activated by containing ozone, oxygen or air to make fuel A method (for example, see Patent Document 1), or a method for producing a fuel containing a fatty acid ester by reacting waste edible oil and alcohol in the presence of a solid catalyst of calcium hydroxide or calcium oxide (for example, see Patent Document 2). Etc. have been proposed.
However, the cost and the means to achieve its desired reference value have not yet been solved, so it appears that it cannot be substituted as part of a mineral oil-based fuel.
その他に食用油として再生再利用する方法も提案されているものの、その処理が困難であり、直接燃焼処理するにもその装置が確立されておらず、使用後の再利用の道がなく、いろいろと検討はされているが、細々と石鹸の製造に環境保護団体等が取り組んでいる程度であり、再利用・リサイクルの開発が待たれている。
また、現在主に金属材料等の切削、切断、セン孔などの加工時に鉱油系、動植物油系、シリコーン等の合成油系など各種の切削油が使用されている。鉱油系切削油に脂肪油あるいはいおう華、硫化脂肪油等を混合したものなどがあるが、使用中に生じる熱で異様な臭気が発生することがあり、また、塩素系のガスを生じるものもある。合成油系のものは高価であり特に精密な切削のみに利用されるだけである。
Although other methods of recycling and reusing as edible oil have been proposed, it is difficult to process, and the apparatus has not been established for direct combustion treatment, and there is no way for reuse after use. However, environmental protection organizations are working on soap production in detail, and the development of reuse and recycling is awaited.
In addition, various cutting oils such as mineral oils, animal and vegetable oils, and synthetic oils such as silicone are currently used mainly for cutting, cutting, and machining of metal materials. There are mineral oil-based cutting oils mixed with fatty oils or sulfur oils, sulfurized fatty oils, etc., but there are cases where strange odors may be generated due to heat generated during use, and those that produce chlorine-based gases is there. Synthetic oils are expensive and are only used for precision cutting.
廃食用油は、主体とする脂肪油中に、調理加熱で酸化変性した脂肪油やその重合体が固体としてあるいは可溶体として含まれており、さらに植物性食材からの炭水化物、肉類からの脂肪、タンパク質、それらの炭化物、更には相当量の水分が分散して含有されている。その他に、工場、家庭等の食用油発生源で貯蔵され運び込まれてくる時の油缶などの容器の鉄と廃食用油中の酸化物との反応による酸化鉄やごみなども不純物として混入しているためその処理手段、実用的な用途を見出すことは困難であった。
本発明は、廃棄され、処分に困っているてんぷら油などのような雑多な不純物を含む廃食用油を簡単に処理し、再生する方法と、それで得られた再生油を有用な切削油等として再利用することを目的とするものである。
Waste cooking oil contains fatty oils and their polymers that are oxidatively modified by cooking and heating as solids or solubles in the main fatty oils, as well as carbohydrates from vegetable ingredients, fats from meat, Proteins, their carbides, and a substantial amount of moisture are dispersed and contained. In addition, iron oxide and waste from the reaction of iron in containers such as oil cans and oxides in waste edible oil when stored and carried in edible oil sources at factories and households are also mixed as impurities. Therefore, it has been difficult to find the processing means and practical use.
The present invention is a method for easily treating and recycling waste edible oil containing miscellaneous impurities such as tempura oil that has been discarded and is difficult to dispose of, and the recycled oil obtained thereby as useful cutting oil, etc. It is intended for reuse.
本発明者らは上記課題に鑑み鋭意研究した結果、初めに廃食用油を浄化しクリーン廃食用油とし、続いてエステル反応を施し、更に精製する工程を組み合わせることを見出し、この知見に基づいて本発明をなすに至った。
すなわち本発明は、
(1)廃食用油をろ過して異物を除去するろ過工程と、その後40〜80℃に加熱して比重分離処理を行いクリーン廃食用油とする比重分離工程と、前記クリーン廃食用油に前記クリーン廃食用油100質量部に対して、10〜15質量部のメタノール(濃度99.9%)及び0・5〜1.5質量部の苛性アルカリ(濃度95.5%)を加えてエステル化を行うエステル化工程と、前記エステル化工程においてエステル化した反応液に、前記反応液の1/3〜2/3容量の40℃〜60℃の温水を加えて攪拌して水洗する水洗工程と、前記水洗工程の後に静置する静置工程と、前記静置工程の後に水相部分を下層部分から除去して油相液体を得る油水分離工程と、前記油相液体に温水を混合し30℃〜80℃に加温して撹拌しながら空気を送り込む曝気工程と、前記曝気工程の後に油水分離を行い水相部分を除去する工程と、ゼオライト、活性白土あるいは澱粉から選ばれる1種以上の吸着剤を前記水相部分を除去した油相液体に加えて撹拌混合して水や未反応物質等を吸着させる吸着処理工程とを有することを特徴とする廃食用油の再生方法、
(2)前記(1)記載の方法で得られた再生油を利用した切削油、
(3)前記(1)記載の方法で得られた再生油を利用した研磨油、浸透油、
(4)前記(1)記載の方法で得られた再生油を利用したディーゼルエンジン油、
(5)前記(1)記載の方法で得られた再生油を利用した保温油及び、
(6)前記(1)記載の方法で得られた再生油を利用した油除去用の液体洗浄液、
を提供するものである。
As a result of diligent research in view of the above problems, the present inventors have found that the waste edible oil is first purified to be a clean waste edible oil, followed by esterification and further refining, based on this finding. It came to make this invention.
That is, the present invention
(1) A filtration step of filtering waste edible oil to remove foreign matters, a specific gravity separation step of heating to 40 to 80 ° C. to perform a specific gravity separation treatment to make a clean waste edible oil, and the clean waste edible oil Esterification by adding 10-15 parts by weight of methanol (concentration 99.9%) and 0.5-1.5 parts by weight of caustic alkali (concentration 95.5%) to 100 parts by weight of clean waste cooking oil An esterification step in which the reaction solution is esterified in the esterification step, and a water washing step in which warm water of 40 ° C to 60 ° C of 1/3 to 2/3 volume of the reaction solution is added and stirred and washed with water , A standing step for standing after the water washing step, an oil / water separation step for removing the water phase portion from the lower layer portion after the standing step to obtain an oil phase liquid, and mixing the warm water with the oil phase liquid. Send air while stirring at 80 ℃ to 80 ℃ An aeration process for removing the water phase by separating oil and water after the aeration process, and at least one adsorbent selected from zeolite, activated clay or starch into an oil phase liquid from which the aqueous phase has been removed. in addition the method of reproducing the waste edible oil, characterized by chromatic and adsorption treatment step of stirring and mixing to adsorb the water and unreacted materials or the like,
(2) Cutting oil using reclaimed oil obtained by the method described in (1) above,
(3) Polishing oil, penetrating oil using regenerated oil obtained by the method described in (1) above,
(4) Diesel engine oil using regenerated oil obtained by the method described in (1) above,
(5) A heat retaining oil using the regenerated oil obtained by the method described in (1) above, and
(6) Liquid cleaning liquid for oil removal using regenerated oil obtained by the method of (1) above,
Is to provide.
本発明の再生方法は、処分に困っていた廃棄された食用油を、きわめて簡単な処理操作で短時間に行うことができ、その実施においても複雑な装置を必要としないし、大きな動力も不用で比較的小規模な設備によって経済的に処理することができる。
そして、得られた再生油はそのままでも、あるいは多少の添加物質を加えることで切削油、研磨油として金属、無機材料はもとより高分子材料等の切削、研磨に利用することができる。また、切削油、研磨油のみならず、浸透油、保温油、ディーゼルエンジン油、液体洗浄油としても有効である。
The regeneration method of the present invention can perform discarded cooking oil, which has been difficult to dispose of, in a short time by a very simple processing operation, and does not require a complicated device for its implementation, and does not require a large amount of power. Can be processed economically with relatively small equipment.
The obtained reclaimed oil can be used as it is, or by adding some additives, it can be used for cutting and polishing cutting materials and polishing oils such as metals and inorganic materials as well as polymer materials. Moreover, it is effective not only as cutting oil and polishing oil but also as permeation oil, heat retaining oil, diesel engine oil, and liquid cleaning oil.
本発明の廃食用油の再生方法の好ましい実施の態様について、図面を参照して詳細に説明する。
一般家庭や外食産業工場からでる使用済みの廃棄される廃食用油は、集荷され廃油タンク(1)に貯蔵される。集められた廃食用油は80〜100メッシュ程度の金属製のスクリーン又は粗目のろ布でろ過(2)処理を行い、含まれるてんぷら滓、集積時に混入するごみ等の固体不純物を除去する。この廃食用油は黒く、粘度が高くどろりとしているので、必要ならば、40℃〜80℃程度に加温し、比重分離(3)処理を行い、ろ過処理で除去できなかった使用中に酸化され、また高分子化された次工程のエステル化反応を阻害する恐れのある物質を排除しておくのがよい。この浄化により得られた廃食用油を以下クリーン廃食用油という。
A preferred embodiment of the method for regenerating waste edible oil of the present invention will be described in detail with reference to the drawings.
Used waste cooking oil from a general household or restaurant industry factory is collected and stored in a waste oil tank (1). The collected edible oil is filtered (2) through a metal screen or coarse filter cloth of about 80 to 100 mesh to remove solid impurities such as tempura koji and dust mixed during accumulation. This waste edible oil is black and thick and thick, so if necessary, heat it to about 40 ° C to 80 ° C, perform specific gravity separation (3), and oxidize during use that could not be removed by filtration. In addition, it is preferable to exclude substances that may inhibit the esterification reaction in the next step, which has been polymerized. The waste edible oil obtained by this purification is hereinafter referred to as clean waste edible oil.
浄化して得られたクリーン廃食用油を撹拌機付きの反応容器に入れ、メタノール及び苛性アルカリ(例として、水酸化カリウムを用いているが、水酸化ナトリウムでもよい)の存在下で30℃〜80℃、好ましくは40℃〜65℃で所定時間ゆっくり撹拌しながらエステル化(4)を行う。このとき、次に示すエステル交換反応(a)と副反応の鹸化(b)、遊離脂肪酸の中和反応(c)が主に生起する。添加するメタノール及び苛性アルカリの量は、クリーン廃食用油100質量部に対し、メタノール(濃度99.9%)10〜15質量部、苛性アルカリ(濃度95.5%)0・5〜1.5質量部が好ましい。 Clean waste edible oil obtained by purification is put into a reaction vessel equipped with a stirrer, and in the presence of methanol and caustic alkali (for example, potassium hydroxide may be used, but sodium hydroxide may be used) Esterification (4) is carried out at 80 ° C., preferably 40 ° C. to 65 ° C. with slow stirring for a predetermined time. At this time, the transesterification (a) and side reaction saponification (b) and neutralization reaction (c) of free fatty acids mainly occur as follows. The amount of methanol and caustic to be added is 10 to 15 parts by mass of methanol (concentration 99.9%), caustic alkali (concentration 95.5%) 0.5 to 1.5 with respect to 100 parts by mass of clean waste cooking oil. Part by mass is preferred.
C3H5(OCOR)3+3CH3OH → 3CH3OOCR+C3H5(OH)3 (a)
C3H5(OCOR)3+3KOH → C3H5(OH)3+3RCOOK (b)
RCOOH+KOH → RCOOK+H2O (c)
C 3 H 5 (OCOR) 3 + 3CH 3 OH → 3CH 3 OOCR + C 3 H 5 (OH) 3 (a)
C 3 H 5 (OCOR) 3 + 3KOH → C 3 H 5 (OH) 3 + 3RCOOK (b)
RCOOH + KOH → RCOOK + H 2 O (c)
反応が終了したら、反応生成物全量を反応容器から分離容器中に移し、反応液の約1/3〜2/3容量、好ましくは約1/2容量の40℃〜60℃の温水を加えて撹拌し、水洗(5)を行った後、30分〜45分間静置(6)する。二層に分離してくるので、下層部分を容器から抜き出し除去する。下層部分は、ラード、グリセリン、副反応で生成した石鹸、未反応物等を含むものであるので、これは後述するように別途利用するように処理する。 When the reaction is complete, transfer the entire amount of the reaction product from the reaction vessel into the separation vessel and add about 1/3 to 2/3 volume, preferably about 1/2 volume of warm water of 40 ° C. to 60 ° C. of the reaction solution. After stirring and washing with water (5), the mixture is allowed to stand (6) for 30 to 45 minutes. Since it is separated into two layers, the lower layer portion is extracted from the container and removed. Since the lower layer portion contains lard, glycerin, soap generated by side reaction, unreacted material, etc., this is treated to be used separately as described later.
分離した上層の液体に温水を混合し30℃〜80℃に加温し、撹拌しながら空気を送り込み曝気(7)により脱気・脱臭をし、静止後に油水分離を行い水相部分を除去する。
この油相液体は、分離できなかった水、余剰のメタノールなど未反応物質等を含んでいるので、続いて、ゼオライト、活性白土あるいは澱粉から選ばれる1種以上の吸着剤をこの液体に加え、容器中で撹拌混合して水、未反応物質等を吸着させ、高級脂肪酸メチルエステルを主成分とする反応物質から分離する吸着(8)処理を行う。吸着剤としては、ゼオライト、活性白土が有効であるが、澱粉でも十分な吸着能を示すので経済的な見地からすれば好ましいものである。
上の撹拌混合物をろ紙袋又はろ布袋に移し入れ、ゆっくりと圧力を掛けて液体を搾り出すこと(ろ過処理(9))により、再生油が得られる。
Hot water is mixed with the separated upper layer liquid, heated to 30 ° C to 80 ° C, air is sent in with stirring, deaeration and deodorization is performed by aeration (7), oil / water separation is performed after resting, and the aqueous phase is removed. .
Since this oil phase liquid contains unreacted substances such as water and excess methanol that could not be separated, subsequently, one or more adsorbents selected from zeolite, activated clay or starch are added to this liquid, The mixture is stirred and mixed in a container to adsorb water, unreacted substances, and the like, and an adsorption (8) treatment is performed to separate the reactants mainly composed of higher fatty acid methyl esters. As the adsorbent, zeolite and activated clay are effective, but starch is also preferable from an economical point of view because it exhibits sufficient adsorbability.
The regenerated oil is obtained by transferring the above stirring mixture into a filter paper bag or a filter cloth bag and slowly applying pressure to squeeze out the liquid (filtering treatment (9)).
得られた再生油は、粘度が高くまた沸点も高い、色相は琥珀色で見た目にもきれいなものである。必要に応じて、周知の添加剤、例えば、油性向上剤、消泡剤、酸化防止剤、清浄分散剤等を加えて、これを切削油として使用するのに好適である。この再生油は、金属や無機材料、硬質高分子材料等の切削工程に使用した場合、高温の発生によっても油中の成分に分解が生起することが少ないためか、いやな臭いが発生することがなく、作業性が極めて良好である。また、この再生油は、単独で使用できるだけでなく、従来使用されている切削油に混入して利用することもできる。 The obtained reclaimed oil has a high viscosity and a high boiling point, and its hue is amber and beautiful in appearance. If necessary, a known additive such as an oil improver, an antifoaming agent, an antioxidant, a cleaning dispersant and the like is added, and this is suitable for use as a cutting oil. When this reclaimed oil is used in the cutting process of metals, inorganic materials, hard polymer materials, etc., the components in the oil are less likely to decompose due to the occurrence of high temperature, or an unpleasant odor will occur. The workability is extremely good. In addition, the reclaimed oil can be used not only alone but also mixed with conventionally used cutting oil.
この再生油は、同様に研磨油としても利用できる。そのうえ、細間隙等への浸透性に優れているので、錆びたねじ、剥離等の処理をする浸透油としても有用であり、暖房、熱交換等の保温油としても好適である。さらに、高級脂肪酸メチルエステルを主成分とする再生油は粘度が高いので、ディーゼルエンジン油として利用することができる。また、油の除去に適している油洗浄剤として利用しても有効である。
また、上記した静置(6)工程で分離された下層部分は、これを水洗い(10)して別途利用する。
This recycled oil can also be used as a polishing oil. In addition, since it has excellent permeability to narrow gaps and the like, it is also useful as a penetrating oil for processing such as rusted screws and peeling, and is also suitable as a heat retaining oil for heating and heat exchange. Furthermore, since regenerated oil mainly composed of higher fatty acid methyl ester has a high viscosity, it can be used as a diesel engine oil. It is also effective when used as an oil cleaning agent suitable for oil removal.
Moreover, the lower layer part isolate | separated by the above-mentioned stationary (6) process is washed with water (10), and is utilized separately.
次に、本発明を実施例に基づいてさらに詳細に説明するが、本発明はこれに制限されるものではない。
(実施例1)
廃食用油タンク1に集められた廃棄食用油を100メッシュの金属製のスクリーンに通し、てんぷら滓、食品屑等の固体不純物を除去した。次いで、約45℃に加温して流動しやすくし、比重分離処理を行ってクリーン廃食用油を得た。このクリーン廃食用油400リットルを加温器、撹拌機付きのステンレス製の反応容器(容量0.8m3)に入れ、50℃に保持した。
一方、メタノール(濃度99.9%)に水酸化カリウムを溶解した、10%水酸化カリウム・メタノール溶液を準備しておき、この水酸化カリウム・メタノール溶液50リットルをクリーン廃食用油の入った反応容器に加え、反応液を約60℃に保って30分間ゆっくり撹拌を繰り返した。
Next, the present invention will be described in more detail based on examples, but the present invention is not limited thereto.
Example 1
The waste edible oil collected in the waste edible oil tank 1 was passed through a 100 mesh metal screen to remove solid impurities such as tempura koji and food waste. Subsequently, it heated to about 45 degreeC, it was made easy to flow, the specific gravity separation process was performed, and the clean waste cooking oil was obtained. 400 liters of this clean waste cooking oil was put into a stainless steel reaction vessel (capacity 0.8 m3) equipped with a heater and a stirrer and kept at 50 ° C.
On the other hand, a 10% potassium hydroxide / methanol solution prepared by dissolving potassium hydroxide in methanol (concentration 99.9%) was prepared, and 50 liters of this potassium hydroxide / methanol solution was added to clean waste cooking oil. In addition to the vessel, the reaction solution was kept at about 60 ° C. and slowly stirred for 30 minutes.
反応の完結した反応生成物を反応容器から分離容器に取り出し、反応液の1/2容量の50℃の温水を添加し、5分間撹拌し、その後40分間静置した。二層に分離したので、沈殿物を含む下層部分を抜き出し、下層部分は別途処理に付した。
分離し残った高級脂肪酸メチルエステルを主成分とする上層の液体に温水を加え約40℃に加温し、撹拌しながら40℃の空気を送り12時間曝気を行った。曝気後、油水分離を行い水相部分を取り除いた。
続いて、この油相液体に4kgの活性白土を加え、撹拌・混合を行い、水、未反応のメタノール等を吸着させた。この混合物をろ布袋に移し入れ、ゆっくりと加圧して液体を搾り出し、琥珀色をした再生油360リットルを得た。
得られた再生油は、引火点178℃、ISO粘度グレード22〜46の脂肪酸メチルエステルを主成分とするものであった。
The reaction product of which reaction was completed was taken out from the reaction vessel into a separation vessel, 1/2 volume of 50 ° C. warm water of the reaction solution was added, stirred for 5 minutes, and then allowed to stand for 40 minutes. Since it separated into two layers, the lower layer part containing a deposit was extracted and the lower layer part was separately processed.
Warm water was added to the upper layer liquid mainly composed of the higher fatty acid methyl ester remaining after separation, and the mixture was heated to about 40 ° C., and aerated at 40 ° C. with stirring for 12 hours. After aeration, oil-water separation was performed to remove the aqueous phase portion.
Subsequently, 4 kg of activated clay was added to the oil phase liquid, and the mixture was stirred and mixed to adsorb water, unreacted methanol, and the like. The mixture was transferred to a filter cloth bag and slowly pressurized to squeeze out the liquid, yielding 360 liters of regenerated oil that was amber.
The obtained reclaimed oil was composed mainly of fatty acid methyl esters having a flash point of 178 ° C. and ISO viscosity grades of 22 to 46.
得られた再生油200リットルに、市販の界面活性剤、酸化防止剤、消泡剤を添加し、切削油として各種の金属材料の切削、切断、穿孔に利用した。これまで使用していた市販の切削油(例えば、扶桑精機(株)製、商品名:マジックカットAM−50,日興産業(株)製、商品名:RIS CUTSY−55,シエル(株)製、商品名:スピードSC−8)と比較し、酸化・劣化が多少早いが、切削性、仕上げ面、刃物損傷などの点で優れたものであった。その上、使用中にいおう臭、塩素臭のような悪臭を感じることがなく作業性が良好であった。
同様に、研磨油、浸透油として利用しても優れたものであった。
Commercially available surfactants, antioxidants, and antifoaming agents were added to 200 liters of the obtained reclaimed oil and used as cutting oil for cutting, cutting, and perforating various metal materials. Commercially available cutting oil used so far (for example, manufactured by Fuso Seiki Co., Ltd., trade name: Magic Cut AM-50, manufactured by Nikko Sangyo Co., Ltd., trade name: RIS CUTSY-55, manufactured by Ciel, Compared with product name: Speed SC-8), oxidation / deterioration was somewhat faster, but it was excellent in terms of machinability, finished surface, damage to the blade, and the like. In addition, the workability was good without feeling bad smell such as smell of smell and chlorine during use.
Similarly, it was excellent when used as a polishing oil or a penetrating oil.
また、得られた再生油に酸化防止剤、錆止め剤、清浄分散剤を添加してディーゼルエンジン油としてエンジン試験に供した。このエンジンオイルは、潤滑膜があり、浸透性が良く、粘度は周知のエンジンオイルと同等なものであるので、市販のエンジンオイルと比較して遜色のないものであった。 Moreover, antioxidant, a rust inhibitor, and a cleaning dispersant were added to the obtained reclaimed oil, and it was subjected to an engine test as a diesel engine oil. This engine oil has a lubricating film, good permeability, and a viscosity equivalent to that of a well-known engine oil, so it was inferior to commercially available engine oil.
さらにまた、得られた再生油を保温油として使用した。市販されているクーラント液、鉱物油系の保温油と比較し、加温時の温度上昇が速く、保温性も2〜3割程度優れており、再生油に添加するグリセリンの量を調整することで、保温の温度調整が可能であった。 Furthermore, the obtained regenerated oil was used as a heat retaining oil. Compared to commercially available coolant fluids and mineral oil-based heat retaining oils, the temperature rises quickly during warming, and the heat retaining properties are excellent by about 20 to 30%. Adjust the amount of glycerin added to the reclaimed oil. Therefore, it was possible to adjust the temperature of heat insulation.
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