JP2009040980A - Method for liquefying and recovering fatty acid and oil-and-fat from waste oil-and-fat containing water and fatty acid - Google Patents

Method for liquefying and recovering fatty acid and oil-and-fat from waste oil-and-fat containing water and fatty acid Download PDF

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JP2009040980A
JP2009040980A JP2007210517A JP2007210517A JP2009040980A JP 2009040980 A JP2009040980 A JP 2009040980A JP 2007210517 A JP2007210517 A JP 2007210517A JP 2007210517 A JP2007210517 A JP 2007210517A JP 2009040980 A JP2009040980 A JP 2009040980A
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fats
oils
fatty acids
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oil
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Hidetoshi Kuramochi
秀敏 倉持
Masahiro Osako
政浩 大迫
Shinichi Sakai
伸一 酒井
Mitsuharu Maeda
光治 前田
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National Institute for Environmental Studies
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    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/10Biofuels, e.g. bio-diesel
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for selectively dehydrating and recovering fatty acids and/or oils and fats from a material containing water and the fatty acids and/or the oils and fats. <P>SOLUTION: Fatty acids and/or oils and fats are selectively dehydrated and recovered from the material containing water and the fatty acids and/or the oils and fats by adding liquefied dimethyl ether (DME) as an extraction medium to the material containing water and the fatty acids and/or oils and fats to bring the fatty acids and the oils and fats to be a liquefied DME solution and selectively dehydrating and recovering the components. The method can be applied to water-containing edible oils and fats, waste edible oils and fats containing water and/or non-oils and fats, waste oils and fats except the waste edible oils and fats, and the like used as the raw material for producing a biodiesel fuel (BDF). By the method, water and the like which are factors inhibiting generation reaction of the BDF can easily and rapidly be removed with low energy from the raw material oils and fats used for producing the BDF. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、水と脂肪酸及び/又は油脂とを含む物質から、脂肪酸及び/又は油脂を選択的に脱水・回収する方法、特に、ディーゼル燃料の製造に際し、水と脂肪酸及び/又は油脂とを含む物質から、ディーゼル燃料の製造用の原料油を調製するために、該水と脂肪酸及び/又は油脂とを含む物質から、脂肪酸及び/又は油脂を選択的に脱水・回収する方法に関する。   The present invention relates to a method for selectively dehydrating and recovering fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils, and in particular, in the production of diesel fuel, water and fatty acids and / or fats and oils are included. The present invention relates to a method for selectively dehydrating and recovering fatty acids and / or fats and oils from a substance containing water and fatty acids and / or fats and oils in order to prepare a raw material oil for producing diesel fuel from the substances.

近年、地球温暖化防止や資源循環の観点から、廃棄物系バイオマスからバイオエタノールやバイオディーゼル燃料(Bio Diesel Fuel:BDF)などのバイオ燃料の製造技術に関する技術開発に注目が集まっている。バイオディーゼル燃料は、ナタネ油、パーム油、オリーブ油、ヒマワリ油、ココナッツ油、大豆油、コメ油等の植物油、牛脂等の獣脂、魚油や、廃食用油などの生物由来の油脂、或いは、トラップグリース(排水表面に浮かぶ泥状の油脂類)のような低品質廃油脂類を原料として合成されるディーゼル燃料(脂肪酸メチルエステル)であり、欧州、北米、中南米、東南アジアなどですでに普及しつつある。   In recent years, from the viewpoint of global warming prevention and resource circulation, attention has been focused on technological development related to manufacturing technology of biofuels such as waste biomass, bioethanol and biodiesel fuel (BDF). Biodiesel fuel is rapeseed oil, palm oil, olive oil, sunflower oil, coconut oil, soybean oil, rice oil, and other vegetable oils, beef tallow and other animal fats, fish oil, and edible oils such as waste edible oil, or trap grease. Diesel fuel (fatty acid methyl ester) synthesized from low-quality waste oils and fats (such as mud oils floating on the surface of drainage), and is already spreading in Europe, North America, Latin America, Southeast Asia, etc. .

バイオディーゼル燃料(BDF)は、油脂類の主成分であるモノグリセリド、ジグリセリド、モノグリセリドを、エタノールのような低級アルコールとエステル交換反応を行なうことにより製造されるが、従来、そのエステル交換反応として、種々の方法が提案されている。例えば、一般的には、油脂類を、NaOH、KOHのようなアルカリ触媒の存在で、メタノールのような低級アルコールを用いてエステル交換反応を行なうアルカリ触媒法が用いられている(特開平7−197047号公報、特開平10−245586号公報、特開2005−350630号公報、特開2005−350631号公報、特開2005−350632号公報)。   Biodiesel fuel (BDF) is produced by subjecting monoglycerides, diglycerides, and monoglycerides, which are the main components of fats and oils, to transesterification with lower alcohols such as ethanol. A method has been proposed. For example, in general, an alkali catalyst method is used in which a fat or oil is subjected to a transesterification reaction using a lower alcohol such as methanol in the presence of an alkali catalyst such as NaOH or KOH (Japanese Patent Laid-Open No. 7-1993). 197047, JP-A-10-245586, JP-A-2005-350630, JP-A-2005-350631, JP-A-2005-350632).

また、温度250〜300℃、圧力3〜15Mpaの温度及び圧力により、アルコールを超臨界状態に保ち、脂肪酸のアルキルエステルを製造する方法(超臨界法)(特開2000−109833号公報、特開2000−143586号公報)、カリウム化合物と酸化ジルコニウムからなる固体塩基性触媒、或いは、ペロブスカイト型構造を有する複合金属酸化物を含んでなる触媒のような固定触媒を用いる方法(特開2000−44984号公報、特開2002−294277号公報)、メチルアミン、ジメチルアミンのような揮発性アミンからなる揮発性触媒を用いる方法(特開2002−167356号公報)等のような各種の方法が提案されている。   Further, a method for producing an alkyl ester of a fatty acid by keeping the alcohol in a supercritical state at a temperature of 250 to 300 ° C. and a pressure of 3 to 15 MPa (supercritical method) (JP 2000-109833, JP 2000-143586), a method using a solid catalyst comprising a potassium compound and zirconium oxide, or a fixed catalyst such as a catalyst comprising a composite metal oxide having a perovskite structure (Japanese Patent Laid-Open No. 2000-44984) Various methods such as a method using a volatile catalyst composed of a volatile amine such as methylamine and dimethylamine (Japanese Patent Laid-Open No. 2002-167356) have been proposed. Yes.

上記のように、バイオディーゼル燃料(BDF)の製造のために、各種の方法が知られているが、これらの方法を用いてバイオディーゼル燃料(BDF)を製造するに際しては、原料として用いる廃油脂類等のバイオディーゼル燃料(BDF)生成反応の阻害物質の除去が必要となる。特に、該バイオディーゼル燃料(BDF)生成反応の阻害物質としては、廃油脂類に含まれる水分や遊離脂肪酸等が問題となる。例えば、アメリカでは、廃食用油に代えて、トラップグリースのようなより低品質な廃油脂類をBDF原料として利用することが検討されている(Trans. ASAE, 44, 1429-1436,2001)。トラップグリースとは、公共下水道排水の前に設置されている阻集器内の排水表面に浮かぶ泥状の油脂類であり、遊離脂肪酸(Free Fatty Acid:FFA)や水分を多く含んでいる。本発明者らの調査では、トラップグリースの油脂中のFFA含有量は約40〜100質量%と高く、また、水分含有量もトラップグリース全体の約20〜60質量%と高かった。   As described above, various methods are known for producing biodiesel fuel (BDF). When producing biodiesel fuel (BDF) using these methods, waste oil used as a raw material is used. It is necessary to remove substances that inhibit the biodiesel fuel (BDF) production reaction. In particular, as an inhibitor of the biodiesel fuel (BDF) production reaction, water, free fatty acids, and the like contained in waste oils and fats are problematic. For example, in the United States, instead of waste cooking oil, use of lower-quality waste fats and oils such as trap grease as BDF raw materials has been studied (Trans. ASAE, 44, 1429-1436, 2001). Trap grease is a muddy oil that floats on the surface of drainage in a collector installed before public sewer drainage, and contains a large amount of free fatty acid (FFA) and water. In the investigation by the present inventors, the FFA content in the fat and oil of the trap grease was as high as about 40 to 100% by mass, and the water content was as high as about 20 to 60% by mass of the entire trap grease.

因みに、水分や遊離脂肪酸(FFA)は、バイオディーゼル燃料(BDF)の生成反応を阻害するため、例えば、BDF製法として現在主流である上記均相アルカリ法では、原料として用い得る油脂類の遊離脂肪酸(FFA)含有量や水分含有量の基準が設定されている(廃棄物学会論文誌、17、193−203、2006)。しかし、それらの基準値は、上記のトラップグリースにおける遊離脂肪酸(FFA)含有量や水分含有量の値の1桁以上低いレベルに設定されている。したがって、トラップグリース等の低品質な廃油脂類を、廃食用油等の比較的高品質な廃油脂類の代わりにそのまま用いることはできず、低品質な廃油脂類を均相アルカリ法などのBDFの製造法に用いるためには、低品質な廃油脂類から脱水したり、遊離脂肪酸(FFA)を除去するなどの前処理が必要とされる。   Incidentally, moisture and free fatty acids (FFA) inhibit the biodiesel fuel (BDF) production reaction. For example, in the above-mentioned homogeneous alkali method, which is currently the mainstream as a BDF production method, free fatty acids of fats and oils that can be used as raw materials Standards for (FFA) content and water content are set (Journal of the Waste Society, 17, 193-203, 2006). However, these reference values are set to a level one digit or more lower than the values of free fatty acid (FFA) content and moisture content in the trap grease. Therefore, low-quality waste oils and fats such as trap grease cannot be used as they are in place of relatively high-quality waste oils and fats such as waste edible oil. In order to use for the manufacturing method of BDF, pre-treatments such as dehydration from low-quality waste oils and fats and removal of free fatty acids (FFA) are required.

バイオディーゼル燃料(BDF)生成反応の阻害物質において、例えば、遊離脂肪酸(FFA)の除去は、遊離脂肪酸(FFA)をメタノールなどのアルコールと反応させて、脂肪酸アルキルエステルを生成することにより達成し得ることが知られている。一方、水分含有量の高い廃油脂や汚泥を脱水する従来の方法として、(減圧)加熱脱水法、フィルタープレス法、遠心分離法などが知られているが、フィルタープレス法や遠心分離法単独では、バイオディーゼル燃料(BDF)の製造法に用い得るレベルまでは脱水することができず、共に(減圧)加熱脱水法を用いる必要がある。また、原料油から遊離脂肪酸を除去するために、原料油を減圧下で温度50〜150℃以下の条件下で遊離脂肪酸を留去する工程を設ける方法も知られている(特開2005−350631号公報)。   In inhibitors of biodiesel fuel (BDF) production reactions, for example, removal of free fatty acids (FFA) can be achieved by reacting free fatty acids (FFA) with alcohols such as methanol to produce fatty acid alkyl esters. It is known. On the other hand, as a conventional method for dewatering waste oil and sludge with a high water content, (decompression) heating dehydration method, filter press method, centrifugation method, etc. are known. However, it cannot be dehydrated to a level that can be used in a method for producing biodiesel fuel (BDF), and it is necessary to use a (depressurized) heating dehydration method. Moreover, in order to remove free fatty acid from raw material oil, a method of providing a step of distilling free fatty acid under reduced pressure at a temperature of 50 to 150 ° C. is known (Japanese Patent Laid-Open No. 2005-350631). Issue gazette).

しかし、実用的なスケールでバイオディーゼル燃料(BDF)を製造するとなると、その原料油脂類は相当な量となり、その原料油脂類に対して(減圧)加熱脱水法を適用する際には、莫大な蒸発潜熱を投入する必要が生じる。そのため、地球環境への影響やコスト面において、十分実用的とはいえなかった。また、低品質な廃油脂類のうち、特にトラップグリースは、泥状やゲル状であることが多く、脱水できたとしても、固体となる場合が多かった。そのため、低品質な廃油脂類を、バイオディーゼル燃料(BDF)の製造等の反応系に適用するには、脱水した上で、更に、適当な溶媒で液化する必要もあった。このように、バイオディーゼル燃料(BDF)の実用的な生産においては、該バイオディーゼル燃料(BDF)の生成反応の阻害物質である、水や、遊離脂肪酸等の分離が重要な課題となっているが、バイオディーゼル燃料(BDF)製造における原料油脂類から、該阻害物質を、低エネルギー、かつ、低コストで有効に分離でき、しかも、各種の原料油脂類に対して適用できる有効な除去方法は、開発されていない。   However, when biodiesel fuel (BDF) is produced on a practical scale, the amount of raw material fats and oils becomes a considerable amount, and when applying the (depressurization) heating dehydration method to the raw material fats and oils, it is enormous. It is necessary to input latent heat of vaporization. For this reason, it has not been practical enough in terms of impact on the global environment and cost. Of the low-quality waste oils and fats, trap grease, in particular, is often in the form of mud or gel, and even if it can be dehydrated, it often becomes a solid. Therefore, in order to apply low-quality waste oils and fats to reaction systems such as the production of biodiesel fuel (BDF), it is also necessary to dehydrate and further liquefy with an appropriate solvent. Thus, in the practical production of biodiesel fuel (BDF), separation of water, free fatty acids, and the like, which are inhibitors of the production reaction of biodiesel fuel (BDF), is an important issue. However, the effective removal method applicable to various raw oils and fats can be effectively separated from the raw oils and fats in the production of biodiesel fuel (BDF) with low energy and low cost. Not developed.

他方、エーテル化合物の一種であり、常温常圧(約0.1MPa)下で気体であり、0.5MPa程度の圧力下では液体となる性状の物質として、ジメチルエーテル(DME)が知られている。ジメチルエーテルは、現在エアゾールの噴射剤として利用されており、また近年は、代替ディーゼルや代替プロパンとしても注目されている。最近、このジメチルエーテルを、脱水に用いる技術が開示されている。例えば、国際公開WO2003/101579号パンフレットには、ジメチルエーテル(DME)の液化物を、水分含有固体(石炭等)に接触させて、この液化ジメチルエーテル(DME)に、固体含有水分を溶解させて、固体の水分を除去する方法が開示されている。   On the other hand, dimethyl ether (DME) is known as a substance that is a kind of ether compound, is a gas under normal temperature and normal pressure (about 0.1 MPa), and becomes liquid under a pressure of about 0.5 MPa. Dimethyl ether is currently used as an aerosol propellant, and has recently attracted attention as an alternative diesel and alternative propane. Recently, a technique using this dimethyl ether for dehydration has been disclosed. For example, in the pamphlet of International Publication No. WO2003 / 101579, a liquefied product of dimethyl ether (DME) is brought into contact with a water-containing solid (such as coal), and the solid-containing water is dissolved in the liquefied dimethyl ether (DME) to obtain a solid. A method for removing the moisture is disclosed.

また、特開2007−83122号公報には、生理用品や紙おむつ、或いはウッドチップや残飯等の含水物質に、ジメチルエーテル等の常温常圧の条件下で気体である物質の液化物を接触させ、該液化物に該含水物質中の水分を溶解させて、含水物質の脱水を行なう方法が開示されている。しかしながら、該開示された方法の対象分野は、バイオディーゼル燃料(BDF)製造に用いられる原料油脂類のようなものとは、全く異なるものであり、その脱水方法そのものもバイオディーゼル燃料(BDF)製造に用いられる原料油脂類に適用されるものとは異なるものである。   In addition, JP 2007-83122 A discloses a liquefied substance of a substance which is a gas under normal temperature and normal pressure conditions such as dimethyl ether to a water-containing substance such as sanitary goods, disposable diapers, or wood chips and leftover rice, A method of dehydrating a water-containing material by dissolving water in the water-containing material in a liquefied product is disclosed. However, the target field of the disclosed method is completely different from the raw oils and fats used for biodiesel fuel (BDF) production, and the dehydration method itself is also biodiesel fuel (BDF) production. It is different from those applied to the raw oils and fats used in the above.

特開平7−197047号公報。JP-A-7-197047. 特開平10−245586号公報。JP-A-10-245586. 特開2000−44984号公報。JP 2000-44984 A. 特開2000−109833号公報。JP 2000-109833 A. 特開2000−143586号公報。JP 2000-143586 A. 特開2002−167356号公報。JP 2002-167356 A. 特開2002−294277号公報。JP 2002-294277 A. 特開2005−350630号公報。JP-A-2005-350630. 特開2005−350631号公報。Japanese Patent Laying-Open No. 2005-350631. 特開2005−350632号公報。JP-A-2005-350632. 特開2007−83122号公報。JP 2007-83122 A. 国際公開WO2003/101579号パンフレットInternational Publication WO2003 / 101579 Pamphlet Trans. ASAE, 44, 1429-1436,2001。Trans. ASAE, 44, 1429-1436, 2001. 廃棄物学会論文誌、17、193−203、2006。Journal of Japan Society for Waste Management, 17, 193-203, 2006.

本発明の課題は、水と脂肪酸及び/又は油脂とを含む物質から、脂肪酸及び/又は油脂を選択的に脱水・回収する方法、特に、バイオディーゼル燃料の製造に際し、水と脂肪酸及び/又は油脂とを含む物質から、バイオディーゼル燃料の製造用として有効に用いることができる原料油を調製するために、該水と脂肪酸及び/又は油脂とを含む物質から、脂肪酸及び/又は油脂を、簡便、迅速かつ低エネルギーで、選択的に脱水・回収する方法を提供することにある。   An object of the present invention is to provide a method for selectively dehydrating and recovering fatty acids and / or fats and oils from a substance containing water and fatty acids and / or fats and oils, in particular, in the production of biodiesel fuel, water and fatty acids and / or fats and oils. In order to prepare a raw material oil that can be effectively used for the production of biodiesel fuel from a substance containing, the fatty acid and / or fat from the substance containing water and fatty acid and / or fat, The object is to provide a method for selective dehydration and recovery quickly and with low energy.

本発明者は、バイオディーゼル燃料(BDF)の製造に際し、水と脂肪酸及び/又は油脂とを含む廃油脂類等から、バイオディーゼル燃料(BDF)の生成反応を阻害する要因となる水分等を、簡便かつ効果的に除去し、バイオディーゼル燃料(BDF)の製造用として有効に用いることができる原料油を調製する方法について、鋭意検討する中で、水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテル(DME)を抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル(DME)溶液として、選択的に脱水、回収することにより、水と脂肪酸及び/又は油脂とを含む物質から、脂肪酸及び/又は油脂の選択的脱水・回収を行うことができることを見い出し、本発明を完成するに至った。   The present inventor, in the production of biodiesel fuel (BDF), from waste oils and fats and the like containing water and fatty acids and / or fats and oils, such as water that becomes a factor that inhibits the production reaction of biodiesel fuel (BDF), As a method for preparing a raw material oil that can be easily and effectively removed and effectively used for the production of biodiesel fuel (BDF), a substance containing water and fatty acids and / or fats and oils has been studied. , By adding liquefied dimethyl ether (DME) as an extraction solvent, and selectively dehydrating and collecting fatty acids and / or fats and oils as liquefied dimethyl ether (DME) solutions, from substances containing water and fatty acids and / or fats and oils, It has been found that selective dehydration and recovery of fatty acids and / or fats and oils can be performed, and the present invention has been completed.

本発明において、脂肪酸及び/又は油脂の選択的脱水・回収を行う水と脂肪酸及び/又は油脂とを含む物質としては、バイオディーゼル燃料(BDF)の製造原料として用いられている水を含有する食用油脂類、水及び/又は非油脂類を含有する廃食用油脂類或いは廃食用油脂類以外の廃油脂類等を挙げることができる。本発明の油脂の選択的脱水・回収方法は、水を含有する油脂類が、泥状又はゲル状の脂肪酸及び/又は油脂の固形物を含有しているものに対しても、有効に適用することができる。   In the present invention, as a substance containing water and fatty acid and / or fats and oils for selective dehydration / recovery of fatty acids and / or fats and oils, edible water containing water used as a raw material for producing biodiesel fuel (BDF) Examples include waste edible fats and oils containing oils and fats, water and / or non-fats, and waste fats and oils other than waste edible fats and oils. The method for selective dehydration / recovery of fats and oils of the present invention is also effectively applied to oils and fats containing water containing mud or gel fatty acids and / or solids of fats and oils. be able to.

本発明の水と脂肪酸及び/又は油脂とを含む物質から、脂肪酸及び/又は油脂を選択的に脱水・回収する方法は、水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテル(DME)を抽出溶媒として添加、攪拌して、液相の均一相を形成し、その後静置して、液化ジメチルエーテル(DME)相と水相との二液相を形成させ、該相より液化ジメチルエーテル(DME)相を分離することにより行うことができる。本発明においては、水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテル(DME)を抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル(DME)溶液として、選択的に脱水、回収するに際し、抽出溶媒に軽油成分を添加することにより、脱水効率を上げ、分離した脂肪酸及び/又は油脂の含水率を1wt%以下の極めて低い含水率とすることができる。かかる場合の軽油成分としては、ヘキサデカン等の炭化水素を挙げることができる。また、軽油成分の添加量としては、抽出処理液全量に対して、10〜50容量%の範囲で添加されることが好ましい。   The method of selectively dehydrating and recovering fatty acids and / or fats and oils from a substance containing water and fatty acids and / or fats and oils according to the present invention includes liquefied dimethyl ether (DME) to a substance containing water and fatty acids and / or fats and oils. Is added as an extraction solvent and stirred to form a homogeneous liquid phase, and then allowed to stand to form a two-liquid phase consisting of a liquefied dimethyl ether (DME) phase and an aqueous phase. ) By separating the phases. In the present invention, liquefied dimethyl ether (DME) is added as an extraction solvent to a substance containing water and fatty acids and / or fats and oils, and the fatty acids and / or fats and oils are selectively dehydrated and recovered as a liquefied dimethyl ether (DME) solution. In doing so, by adding a light oil component to the extraction solvent, the dehydration efficiency can be increased, and the water content of the separated fatty acids and / or fats and oils can be set to a very low water content of 1 wt% or less. Examples of the light oil component in such a case include hydrocarbons such as hexadecane. Moreover, as addition amount of a light oil component, it is preferable to add in 10-50 volume% with respect to the extraction processing liquid whole quantity.

本発明において、水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテル(DME)を抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル(DME)溶液として、選択的に脱水、回収する処理は、温度10〜35℃の範囲で行なうことが好ましい。特に、該選択的脱水、回収処理における温度を、30〜35℃の範囲に調節して行なうことにより、脱水効率を上げ、分離した脂肪酸及び/又は油脂の含水率を1〜3wt%低い含水率とすることができる。   In the present invention, liquefied dimethyl ether (DME) is added as an extraction solvent to a substance containing water and fatty acids and / or fats and oils, and the fatty acids and / or fats and oils are selectively dehydrated and recovered as a liquefied dimethyl ether (DME) solution. The treatment is preferably performed at a temperature in the range of 10 to 35 ° C. In particular, the temperature in the selective dehydration and recovery treatment is adjusted to the range of 30 to 35 ° C. to increase the dehydration efficiency, and the water content of the separated fatty acid and / or fat is reduced by 1 to 3 wt%. It can be.

また、本発明は、本発明の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法により、脱水された脂肪酸及び/又は油脂と、液化ジメチルエーテル(DME)とを含む物質を調製することからなる、バイオディーゼル燃料(BDF)製造のための原料油の調製方法を包含する。該バイオディーゼル燃料(BDF)の製造法としては、特に限定されないが、液化ジメチルエーテル(DME)を添加した均一相系でのエステル交換反応を行なうバイオディーゼル燃料の製造法の原料油の調製方法(別途、特許出願:特願2007−210501)に適用して、極めて有利な効果を得ることができる。すなわち、本発明における選択的に脱水、回収される脂肪酸及び/又は油脂は、液化ジメチルエーテル(DME)の溶液として、回収することができ、かかる油脂類はそのままバイオディーゼル燃料(BDF)製造のための原料油として用いることができ、更に、含有される液化ジメチルエーテル(DME)もそのままバイオディーゼル燃料(BDF)の製造に利用することができるからである。   Further, the present invention provides a method for selectively dehydrating and recovering fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils of the present invention, and dehydrated fatty acids and / or fats and liquefied dimethyl ether (DME). And a method for preparing a feedstock for the production of biodiesel fuel (BDF). A method for producing the biodiesel fuel (BDF) is not particularly limited, but a method for preparing a raw material oil in a method for producing a biodiesel fuel in which a transesterification reaction is performed in a homogeneous phase system to which liquefied dimethyl ether (DME) is added (separately , Patent application: Japanese Patent Application No. 2007-210501), extremely advantageous effects can be obtained. That is, the fatty acids and / or fats and oils selectively dehydrated and recovered in the present invention can be recovered as a solution of liquefied dimethyl ether (DME), and these fats and oils can be directly used for producing biodiesel fuel (BDF). This is because it can be used as a raw material oil, and the liquefied dimethyl ether (DME) contained can be used as it is for the production of biodiesel fuel (BDF).

更に、本発明のバイオディーゼル燃料(BDF)製造のための原料油の調製方法は、酸触媒、低級アルコールを用いた遊離脂肪酸のエステル化反応と併用して行なうことができる。該酸触媒、低級アルコールを用いた遊離脂肪酸のエステル化反応により、バイオディーゼル燃料(BDF)の製造に用いられる原料油脂類に含有される遊離脂肪酸を、エステル化(バイオディーゼル燃料化)して、バイオディーゼル燃料(BDF)の生成反応を阻害する要因となる水分及び遊離脂肪酸を同時に除去することができる。   Furthermore, the method for preparing a raw material oil for the production of biodiesel fuel (BDF) of the present invention can be carried out in combination with an esterification reaction of free fatty acid using an acid catalyst and a lower alcohol. By esterifying the free fatty acid using the acid catalyst and lower alcohol, the free fatty acid contained in the raw fats and oils used in the production of biodiesel fuel (BDF) is esterified (biodiesel fuel), It is possible to simultaneously remove water and free fatty acids that are factors that inhibit the production reaction of biodiesel fuel (BDF).

すなわち具体的には本発明は、(1)水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル溶液として、選択的に脱水、回収することを特徴とする水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法や、
(2)水と脂肪酸及び/又は油脂とを含む物質が、水を含有する食用油脂類、水及び/又は非油脂類を含有する廃食用油脂類或いは廃食用油脂類以外の廃油脂類であることを特徴とする上記(1)記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法や、
(3)水と脂肪酸及び/又は油脂とを含む物質が、泥状又はゲル状の脂肪酸及び/又は油脂の固形物を含有していることを特徴とする上記(1)又は(2)記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法や、
(4)水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加、攪拌して、液相の均一相を形成し、その後静置して、液化ジメチルエーテル相と水相との二液相を形成させ、該相より液化ジメチルエーテル相を分離することよりなる上記(1)〜(3)のいずれか記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法や、
(5)水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル溶液として、選択的に脱水、回収するに際し、抽出溶媒に軽油成分を添加することを特徴とする上記(1)〜(4)のいずれか記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法や、
(6)軽油成分の添加が、抽出処理液全量に対して、10〜50容量%の範囲で添加されることを特徴とする上記(5)記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法や、
(7)水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル溶液として、選択的に脱水、回収する処理を、温度10〜35℃の範囲で行なうことを特徴とする上記(1)〜(6)のいずれか記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法や、
(8)水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル溶液として、選択的に脱水、回収する処理を、温度30〜35℃の範囲に調整して行なうことを特徴とする上記(7)記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法からなる。
Specifically, the present invention specifically comprises (1) adding a liquefied dimethyl ether as an extraction solvent to a substance containing water and a fatty acid and / or fat, and selectively dehydrating the fatty acid and / or fat as a liquefied dimethyl ether solution. A method for selectively dehydrating and recovering fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils,
(2) Substances containing water and fatty acids and / or fats and oils are edible fats and oils containing water, waste edible fats and oils containing water and / or non-fats or waste fats and oils other than waste edible fats and oils The method for selective dehydration and recovery of fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils as described in (1) above,
(3) The substance according to (1) or (2) above, wherein the substance containing water and fatty acids and / or fats and oils contains a solid matter of mud or gel fatty acids and / or fats and oils A method for selective dehydration and recovery of fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils;
(4) Add liquefied dimethyl ether as an extraction solvent to a substance containing water and fatty acids and / or fats and oils, and stir to form a uniform liquid phase; And / or a fatty acid from a substance containing water and a fatty acid and / or an oil and fat according to any one of the above (1) to (3), wherein the liquefied dimethyl ether phase is separated from the phase. A method for selective dehydration and recovery of fats and oils,
(5) When a liquefied dimethyl ether is added as an extraction solvent to a substance containing water and fatty acids and / or fats and oils, and the fatty acids and / or fats and oils are selectively dehydrated and recovered as a liquefied dimethyl ether solution, A method for selectively dehydrating and recovering fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils according to any one of (1) to (4) above,
(6) The substance containing water and fatty acids and / or fats and oils according to (5) above, wherein the light oil component is added in an amount of 10 to 50% by volume based on the total amount of the extraction treatment liquid. For selective dehydration and recovery of fatty acids and / or fats from
(7) A process in which liquefied dimethyl ether is added as an extraction solvent to a substance containing water and fatty acids and / or fats and oils, and the fatty acid and / or fats and oils are selectively dehydrated and recovered as a liquefied dimethyl ether solution at a temperature of 10 to 35. The method for selective dehydration and recovery of fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils according to any one of (1) to (6),
(8) A process in which liquefied dimethyl ether is added as an extraction solvent to a substance containing water and fatty acids and / or fats and oils, and the fatty acid and / or fats and oils are selectively dehydrated and recovered as a liquefied dimethyl ether solution at a temperature of 30 to 35. The method comprises the method for selective dehydration / recovery of fatty acids and / or fats and oils from a substance containing water and fatty acids and / or fats and oils according to the above (7), which is carried out by adjusting the temperature to a range of ° C.

また本発明は、(9)上記(1)〜(8)のいずれか記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法により、脱水された脂肪酸及び/又は油脂と、液化ジメチルエーテルとを含む物質を調製することを特徴とする、バイオディーゼル燃料製造のための原料油の調製方法や、
(10)バイオディーゼル燃料の製造が、液化ジメチルエーテルを添加した均一相系でのエステル交換反応を行なう方法によるものであることを特徴とする上記(9)記載のバイオディーゼル燃料製造のための原料油の調製方法や、
(11)バイオディーゼル燃料製造のための原料油の調製が、酸触媒、低級アルコールを用いた遊離脂肪酸のエステル化反応と併用して行なわれることを特徴とする上記(9)又は(10)記載のバイオディーゼル燃料製造のための原料油の調製方法からなる。
Further, the present invention is (9) dehydrated by the method for selective dehydration / recovery of fatty acids and / or fats from substances containing water and fatty acids and / or fats and oils according to any one of (1) to (8) above. A method for preparing a raw material oil for biodiesel fuel production, characterized in that a substance containing fatty acid and / or fat and oil and liquefied dimethyl ether is prepared,
(10) The feedstock for producing biodiesel fuel according to (9) above, wherein the biodiesel fuel is produced by a method of transesterification in a homogeneous phase system to which liquefied dimethyl ether is added The preparation method of
(11) The above (9) or (10), wherein the preparation of the raw material oil for the production of biodiesel fuel is carried out in combination with an esterification reaction of a free fatty acid using an acid catalyst and a lower alcohol. The method for preparing a feedstock for the production of biodiesel.

本発明によれば、バイオディーゼル燃料(BDF)の製造に際し、水と脂肪酸及び/又は油脂とを含む廃油脂類等から、バイオディーゼル燃料(BDF)の生成反応を阻害する要因となる水分等を、従来のような加熱処理や減圧処理を用いることなく、低エネルギーで、簡便かつ効果的に除去することが可能であり、バイオディーゼル燃料(BDF)の製造における実用化技術として、極めて高い有用性を有する。特に、本発明の方法は、バイオディーゼル燃料(BDF)の製造原料として用いられている水を含有する食用油脂類、水及び/又は非油脂類を含有する廃食用油脂類或いは廃食用油脂類以外の廃油脂類等の広い範囲の油脂類に適用することができ、トラップグリースなどの特に低品質な廃油脂類からも、バイオディーゼル燃料を製造することが可能な原料油を、迅速かつ低エネルギーで調製することができ、環境対策の点でも非常に有用である。   According to the present invention, in the production of biodiesel fuel (BDF), water and the like that are factors that inhibit the production reaction of biodiesel fuel (BDF) from waste oils and fats containing water and fatty acids and / or fats and oils. It can be removed easily and effectively with low energy without using conventional heat treatment and decompression treatment, and it is extremely useful as a practical technology in the production of biodiesel fuel (BDF). Have In particular, the method of the present invention is applicable to edible fats and oils containing water, used as a raw material for producing biodiesel fuel (BDF), waste edible fats and oils or waste edible fats and oils containing water and / or non-fats. It can be applied to a wide range of fats and oils such as waste oils and fats, and raw oils that can produce biodiesel fuel from waste oils and fats of particularly low quality such as trap greases can be quickly and low-energy It is also very useful in terms of environmental measures.

更に、本発明の方法によって、調製されるバイオディーゼル燃料(BDF)の製造用原料油は、バイオディーゼル燃料(BDF)の生成反応を阻害する要因となる水分等を、簡便かつ効果的に除去したということにとどまらず、該原料油を用いたバイオディーゼル燃料(BDF)の生成反応を促進し、更に、該バイオディーゼル燃料(BDF)の生成反応によって、生成された反応液からのバイオディーゼル燃料(BDF)成分の分離、回収を簡便かつ容易に行うことを可能とするという、バイオディーゼル燃料(BDF)の製造における極めて高い実用上の効果をもたらすものである。したがって、本発明の技術は、バイオディーゼル燃料(BDF)の実用化に、多大の貢献を有するものである。   Furthermore, the raw material oil for production of biodiesel fuel (BDF) prepared by the method of the present invention can easily and effectively remove moisture and the like that inhibit the biodiesel fuel (BDF) formation reaction. In addition to that, the biodiesel fuel (BDF) production reaction using the raw oil is promoted, and further, the biodiesel fuel (BDF) produced from the reaction liquid produced by the biodiesel fuel (BDF) production reaction ( The BDF component can be easily and easily separated and recovered, and this has a very high practical effect in the production of biodiesel fuel (BDF). Therefore, the technology of the present invention has a great contribution to the practical application of biodiesel fuel (BDF).

本発明は、水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル溶液として、選択的に脱水、回収することを特徴とする水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法からなる。なお、本発明における「脱水」には、水分を完全に除去する場合だけでなく、水分を減少させる場合も包含される。   The present invention is characterized in that liquefied dimethyl ether is added as an extraction solvent to a substance containing water and fatty acids and / or fats and oils, and the fatty acids and / or fats and oils are selectively dehydrated and recovered as a liquefied dimethyl ether solution. And a method for selective dehydration and recovery of fatty acids and / or fats and oils from substances containing fatty acids and / or fats and oils. The “dehydration” in the present invention includes not only the case where moisture is completely removed but also the case where moisture is reduced.

本発明の脱水方法に用いる、水と脂肪酸及び/又は油脂とを含む物質としては、水と脂肪酸及び/又は油脂とを含んでいる物質である限り特に制限されないが、
バイオディーゼル燃料(BDF)の製造原料として用いられている水を含有する食用油脂類、水及び/又は非油脂類を含有する廃食用油脂類或いは廃食用油脂類以外の廃油脂類等が例示される。また、該廃油脂類としては、固体状、液体状、ゲル状、泥状等のいずれの前記物質であっても用いることができ、具体的には、トラップグリース(公共下水道排水の前に設置されている阻集器内の排水表面に浮かぶ泥状の油脂含有物)や、水を含んだ廃食用油(液体状、固体状、ゲル状等)などを例示することができる。
The substance containing water and fatty acid and / or fat used in the dehydration method of the present invention is not particularly limited as long as it is a substance containing water and fatty acid and / or fat,
Examples include edible fats and oils containing water used as a raw material for producing biodiesel fuel (BDF), waste edible fats and oils containing water and / or non-fats, and waste fats and oils other than waste edible fats and oils, etc. The Further, as the waste oils and fats, any of the above-mentioned substances such as solid, liquid, gel, and mud can be used. Specifically, trap grease (installed before public sewer drainage) Examples thereof include muddy oils and fats floating on the drainage surface in the interceptor and waste edible oil (liquid, solid, gel, etc.) containing water.

上記脂肪酸としては、特に制限されず、飽和脂肪酸、不飽和脂肪酸、分岐脂肪酸、ヒドロキシル脂肪酸等のいずれであってもよいが、C12〜C28の脂肪酸からなる群から選ばれる1種又は2種以上の脂肪酸を好ましく例示することができ、具体的には、ラウリン酸、ミリスチン酸、ペンタデシル酸、パルミチン酸、パルミトイル酸、ステアリン酸、リノール酸、リノレイン酸、アラキドン酸等を好適に例示することができる。   The fatty acid is not particularly limited and may be any of saturated fatty acid, unsaturated fatty acid, branched fatty acid, hydroxyl fatty acid and the like, but one or more selected from the group consisting of C12 to C28 fatty acids. Fatty acids can be preferably exemplified, and specifically, lauric acid, myristic acid, pentadecylic acid, palmitic acid, palmitoyl acid, stearic acid, linoleic acid, linolenic acid, arachidonic acid and the like can be suitably exemplified.

上記油脂としては、特に制限されず、トリグリセリド、ジグリセリド、モノグリセリド等のいずれであってもよいが、トリグリセリドであることが好ましく、トリグリセリンの構成脂肪酸がC12〜C28の脂肪酸からなる群から選ばれる1種又は2種以上の脂肪酸であるトリグリセリドをより好ましく例示することができる。上記油脂として具体的には、大豆油、ゴマ油、ナタネ油、コメ油、ヌカ油、ツバキ油、サフラワー油 (ベニバナ油)、パーム油、パーム殻油、ヤシ油、綿実油、ヒマワリ油、荏油、オリーブオイル、ピーナッツオイル、アーモンドオイル、アボカドオイル、ヘーゼルナッツオイル、ウォルナッツオイル、グレープシードオイル、魚油、肝油、鮫油等の油や、ラード(豚脂)、ヘット(牛脂)、鶏油、シュマルツ、ショートニング、バター、マーガリン、カカオバター、硬化油等の脂肪を例示することができる。この他、非食用の植物油脂も用いることができる。   The oil and fat is not particularly limited and may be any of triglyceride, diglyceride, monoglyceride, etc., but is preferably triglyceride, and the constituent fatty acid of triglycerin is selected from the group consisting of C12 to C28 fatty acids. A triglyceride which is a seed or two or more fatty acids can be exemplified more preferably. Specific examples of the fats and oils include soybean oil, sesame oil, rapeseed oil, rice oil, nutka oil, camellia oil, safflower oil (safflower oil), palm oil, palm shell oil, coconut oil, cottonseed oil, sunflower oil, coconut oil , Olive oil, peanut oil, almond oil, avocado oil, hazelnut oil, walnut oil, grape seed oil, fish oil, liver oil, salmon oil and other oils, lard (pig fat), het (beef tallow), chicken oil, schmalz And fats such as shortening, butter, margarine, cocoa butter, hydrogenated oil, and the like. In addition, non-edible vegetable fats and oils can also be used.

上記の本発明の物質には、水と脂肪酸及び/又は油脂以外に、繊維質等の固形分などの任意の成分をさらに含んでいてもよい。なお、上記本発明の物質の含水率は特に制限されないが、本発明の脱水方法のメリットをより多く享受する観点からは、本発明の物質全量に対して10wt%以上であることが好ましく、20wt%以上であることがより好ましく、40wt%以上であることがさらに好ましい。   In addition to water and fatty acids and / or fats and oils, the substance of the present invention may further contain an optional component such as a solid content such as fiber. The water content of the substance of the present invention is not particularly limited, but from the viewpoint of enjoying more benefits of the dehydration method of the present invention, it is preferably 10 wt% or more based on the total amount of the substance of the present invention, 20 wt% % Or more is more preferable, and it is further more preferable that it is 40 wt% or more.

本発明において、水と脂肪酸及び/又は油脂とを含む物質から、脂肪酸及び/又は油脂を選択的に脱水・回収するには、水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加、攪拌して、液相の均一相を形成し、その後静置して、液化ジメチルエーテル相と水相との二液相を形成させ、該相より液化ジメチルエーテル相を分離することにより行われるが、本発明の脱水・回収方法の工程におけるエーテル相と水相との二液相の形成は、例えば、本発明の物質にエーテル化合物を含有させた後、静置や遠心するなどして下相の水相と、上相のエーテル相に分離させることによって行うことができるが、より高い脱水効率をより簡便に得る観点からは、本発明の物質にエーテル化合物を含有させた後に攪拌してから静置することが好ましい。また、本発明の物質中に固形物が含まれている場合は、通常沈殿し、下相である水相に移行する。   In the present invention, in order to selectively dehydrate and recover fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils, liquefied dimethyl ether is extracted into substances containing water and fatty acids and / or fats and oils. It is added and stirred as a solvent to form a homogeneous liquid phase, and then allowed to stand to form a two-liquid phase of a liquefied dimethyl ether phase and an aqueous phase, and the liquefied dimethyl ether phase is separated from the phase. However, the formation of the two-liquid phase of the ether phase and the aqueous phase in the process of the dehydration / recovery method of the present invention is, for example, by allowing the substance of the present invention to contain an ether compound, and then allowing it to stand or centrifuge. Although it can be carried out by separating the lower phase water phase and the upper phase ether phase, from the viewpoint of more easily obtaining higher dehydration efficiency, the substance of the present invention is mixed with an ether compound and stirred. The Luo it is preferable to standing. Moreover, when the solid substance is contained in the substance of the present invention, it usually precipitates and shifts to the lower aqueous phase.

上記脱水・回収方法の工程において、本発明の物質に含有させるエーテル化合物の量は、特に制限されないが、一方で、本発明の物質中の脂肪酸や油脂を溶解するのに十分な量であることが好ましく、他方で、多すぎると脱水効率が若干低下する場合があるため、両方をバランスさせることが好ましく、本発明の物質中の脂肪酸や油脂を飽和濃度近傍で溶解する量であることが最も好ましい。   In the step of the dehydration / recovery method, the amount of the ether compound to be contained in the substance of the present invention is not particularly limited, but on the other hand, it should be an amount sufficient to dissolve the fatty acid and fat in the substance of the present invention. On the other hand, if it is too much, the dehydration efficiency may be slightly reduced. Therefore, it is preferable to balance both, and the amount that dissolves fatty acids and fats and oils in the substance of the present invention near the saturation concentration is the most. preferable.

本発明の脱水・回収方法の工程における水相を除去する方法は特に制限されず、エーテル相を二液相から回収してもよいし、二液相から水相を除去してもよい。二液相から水相を除去することによって、加熱処理や減圧処理を用いることなく、本発明の物質を簡便、迅速かつ低エネルギーで脱水することができる。また、水相を除去して得られたエーテル相において、本発明の物質中の脂肪酸及び/又は油脂を極めて高い収率で抽出することができる。   The method for removing the aqueous phase in the process of the dehydration / recovery method of the present invention is not particularly limited, and the ether phase may be recovered from the two liquid phases, or the aqueous phase may be removed from the two liquid phases. By removing the aqueous phase from the two-liquid phase, the substance of the present invention can be dehydrated simply, rapidly and with low energy without using heat treatment or reduced pressure treatment. Moreover, in the ether phase obtained by removing the aqueous phase, fatty acids and / or fats and oils in the substance of the present invention can be extracted with a very high yield.

本発明の脱水方法は、バイオディーゼル燃料(BDF)製造用の原料油脂及び/又は原料脂肪酸の前処理方法として好適に用いることができる。すなわち、上記本発明の物質にエーテル化合物を含有させて、エーテル相と水相の二液相を形成させ、水相を除去すること等によって、バイオディーゼル燃料(BDF)製造用の原料油脂及び/又は原料脂肪酸溶液としてのエーテル相溶液を得ることができる。この前処理によって得られた原料油脂及び/又は原料脂肪酸を含むこのエーテル相溶液に、メタノール及び適当な触媒を含有させてメチルエステル化反応を行うことによって、バイオディーゼル燃料(BDF)(脂肪酸メチルエステル)を好適に製造することができる。   The dehydration method of the present invention can be suitably used as a pretreatment method for raw oils and / or raw fatty acids for producing biodiesel fuel (BDF). That is, by adding an ether compound to the substance of the present invention to form a two-liquid phase of an ether phase and an aqueous phase and removing the aqueous phase, the raw oil and fat for producing biodiesel fuel (BDF) and / or Alternatively, an ether phase solution as a raw fatty acid solution can be obtained. Biodiesel fuel (BDF) (fatty acid methyl ester) is obtained by carrying out a methyl esterification reaction by adding methanol and a suitable catalyst to the ether phase solution containing the raw oil and fat and / or raw fatty acid obtained by this pretreatment. ) Can be suitably produced.

上記前処理方法における上記エーテル相溶液のエーテルとしては、相分離性に優れ、毒性もより低く、バイオディーゼル燃料(BDF)の製造の際のコスト及び環境対策の点でより優れ、また、液化ジメチルエーテル(DME)は代替軽油としても用いられるため、バイオディーゼル燃料(BDF)中に仮に混入したとしても問題が少ないと考えられることから、ジメチルエーテル(DME)であることが特に好ましい。例えば、原料油脂及び/又は原料脂肪酸を含む液化ジメチルエーテル(DME)相を用いてバイオディーゼル燃料(BDF)の製造を行うと、バイオディーゼル燃料(BDF)を含む液化ジメチルエーテル(DME)相中のジメチルエーテル(DME)を気化させてジメチルエーテル(DME)を容易に回収することができ、副生物であるグリセリンを含むグリセリン相中のメタノールを、前述の回収した液化ジメチルエーテル(DME)を用いて減圧蒸留を行うことなく抽出することができる点で、コスト及び環境対策の点でより優れている。   As the ether of the ether phase solution in the pretreatment method, the phase separation property is excellent, the toxicity is lower, the cost in the production of biodiesel fuel (BDF) and the environmental measures are superior, and liquefied dimethyl ether. Since (DME) is also used as an alternative light oil, dimethyl ether (DME) is particularly preferable because it is considered that there are few problems even if it is mixed in biodiesel fuel (BDF). For example, when biodiesel fuel (BDF) is produced using a liquefied dimethyl ether (DME) phase containing raw oil and / or fatty acid, dimethyl ether (DME) in a liquefied dimethyl ether (DME) phase containing biodiesel fuel (BDF) ( DME) can be vaporized to easily recover dimethyl ether (DME), and methanol in the glycerin phase containing glycerin as a by-product is distilled under reduced pressure using the recovered liquefied dimethyl ether (DME). It is superior in terms of cost and environmental measures because it can be extracted without any problems.

本発明において、低品質廃油脂類のように、エステル交換反応に用いる原料油中に、多量の遊離脂肪酸及び水を含む廃油脂類の場合には、本発明の脂肪酸及び/又は油脂の選択的脱水・回収方法と併用して、酸触媒、低級アルコールを用いた遊離脂肪酸のエステル化反応を行ない、原料油脂類に含有される遊離脂肪酸を、エステル化(バイオディーゼル燃料化)して、バイオディーゼル燃料(BDF)の生成反応を阻害する要因となる水分及び遊離脂肪酸を同時に除去することができる。すなわち、廃油脂類を、酸触媒の存在下、遊離脂肪酸を液化ジメチルエーテル(DME)を添加した均一相にて、低級アルコールによりエステル化反応を行い、遊離脂肪酸等から脂肪酸メチルエステルを生成して原料物質中の遊離脂肪酸濃度を低下させることができ、次いで、液化ジメチルエーテルで溶媒抽出を行なうことにより、エーテル相(上相)と水相(下相)の二液相を形成させ、前記水相を除去することによって、脱水処理を行うことにより、蒸発潜熱を加えることなく、低エネルギー、低コストにて原料物質を脱水し、遊離脂肪酸の除去と脱水を行なって、エステル交換反応に用いる原料油を調製することができる。   In the present invention, in the case of waste oils and fats containing a large amount of free fatty acids and water in the raw material oil used for the transesterification reaction, such as low-quality waste oils and fats, the fatty acids and / or fats and oils of the present invention are selectively used. Combined with the dehydration and recovery method, esterification of free fatty acids using acid catalysts and lower alcohols is performed, and free fatty acids contained in raw oils and fats are esterified (biodiesel fuel) to produce biodiesel It is possible to simultaneously remove moisture and free fatty acids that are factors that inhibit the production reaction of fuel (BDF). That is, waste oils and fats are subjected to an esterification reaction with a lower alcohol in a homogeneous phase in which free fatty acids are added with liquefied dimethyl ether (DME) in the presence of an acid catalyst to produce fatty acid methyl esters from the free fatty acids and the like. The concentration of free fatty acids in the substance can be reduced, and then solvent extraction with liquefied dimethyl ether forms a two-liquid phase of an ether phase (upper phase) and an aqueous phase (lower phase). By removing the dehydration treatment, the raw material is dehydrated at low energy and low cost without adding latent heat of vaporization, and free fatty acids are removed and dehydrated to obtain the raw oil used in the transesterification reaction. Can be prepared.

以下、実施例により本発明をより具体的に説明するが、本発明の技術的範囲はこれらの例示に限定されるものではない。   EXAMPLES Hereinafter, although an Example demonstrates this invention more concretely, the technical scope of this invention is not limited to these illustrations.

[水及び脂肪酸を高濃度で含有する廃油脂の液化DMEを用いた脱水、並びに、脂肪酸及び油脂の選択的回収 1]
(実験方法)
エーテル化合物の1種である液化DMEを用いて、水及び脂肪酸を高濃度で含有する廃油脂(高含水及び高脂肪酸含有廃油脂)から、脂肪酸及び油脂を回収し得るかを調べるために、図1に示した一連の装置を使用して以下の実験を行った:まず、トリオレイン9g、パルミチン酸6g及び水3.75gを混合して、高含水及び高脂肪酸含有廃油脂モデル溶液(以下、「廃油脂モデル溶液」ともいう)を調製した。この廃油脂モデル溶液18.75gを、耐圧ガラスセル(A)に添加し、該セルを氷水に浸して、廃油脂モデル溶液を10℃以下程度に冷却した。その後、バルブ(C)を開いて、ガラスシリンダー(B)中の液化DMEをガラスセル(A)内に導入し、液化DMEがガラスセル(A)に約11g入ったところでバルブ(C)を閉めた。次に、温度コントローラー(D)の温度を25℃に設定し、ガラスセル(A)内の溶液が設定温度になるまで加熱攪拌した。水相の生成と固体のパルミチン酸が完全に溶解することを確認した後、ガラスセル(A)内の溶液を15分静置した。ガラスセル(A)内の溶液は、上相の液化DME相と、下相の水相に分かれた。
[Dehydration of waste oils and fats containing high concentrations of water and fatty acids using liquefied DME, and selective recovery of fatty acids and oils and fats 1]
(experimental method)
In order to investigate whether fatty acids and fats can be recovered from waste oils and fats containing high concentrations of water and fatty acids (high water content and high fatty acid content waste fats and oils) using liquefied DME, which is one of the ether compounds, The following experiment was conducted using the series of apparatuses shown in Fig. 1: First, 9 g of triolein, 6 g of palmitic acid and 3.75 g of water were mixed, and a high oil content and high fatty acid content waste oil model solution (hereinafter, Also referred to as “waste oil / fat model solution”. 18.75 g of this waste oil / fat model solution was added to the pressure-resistant glass cell (A), the cell was immersed in ice water, and the waste oil / fat model solution was cooled to about 10 ° C. or less. Thereafter, the valve (C) is opened, and the liquefied DME in the glass cylinder (B) is introduced into the glass cell (A). When about 11 g of liquefied DME enters the glass cell (A), the valve (C) is closed. It was. Next, the temperature of the temperature controller (D) was set to 25 ° C., and the mixture was heated and stirred until the solution in the glass cell (A) reached the set temperature. After confirming that the aqueous phase was formed and the solid palmitic acid was completely dissolved, the solution in the glass cell (A) was allowed to stand for 15 minutes. The solution in the glass cell (A) was divided into an upper liquefied DME phase and a lower aqueous phase.

次いで、バルブ(E)を開くことによって液化DME回収ライン(F)から流出した液化DME相に抽出された固体状の油脂や脂肪酸をサンプルびん(G)にてサンプリングした。その後、サンプリングした固体(固体サンプル)の水分量を、カールフィッシャー水分計にて測定した。一方、バルブ(H)を開いて、水相回収ライン(I)から流出した水相をサンプルびん(J)にサンプリングした。サンプリングした水溶液をイソプロパノールで希釈し、高速液体クロマトグラフにてトリオレイン及びパルミチン酸の濃度を測定した。   Subsequently, the solid oil and fatty acid extracted to the liquefied DME phase which flowed out from the liquefied DME collection | recovery line (F) by opening a valve | bulb (E) was sampled in the sample bottle (G). Thereafter, the moisture content of the sampled solid (solid sample) was measured with a Karl Fischer moisture meter. On the other hand, the valve (H) was opened, and the aqueous phase flowing out from the aqueous phase recovery line (I) was sampled in a sample bottle (J). The sampled aqueous solution was diluted with isopropanol, and the concentrations of triolein and palmitic acid were measured with a high performance liquid chromatograph.

(結果)
上記水分計の測定の結果、この固体サンプルの含水率は約2.5wt%〜3.0wt%程度であった。実験前の廃油脂モデル溶液の含水率(20wt%)と比較すると水分量が1/7〜1/8へ減少したこととなり、液化DMEによる液化抽出によって、廃油脂モデル溶液を効率よく脱水し得ることが明らかとなった。また、温度コントローラー(D)の温度を35℃に設定し、液化DMEの添加量を9.75gとしたこと以外は同じ手順で実験を行ったところ、固体サンプルの含水率は約1.4wt%であった。さらに、温度コントローラー(D)の温度を35℃に設定し、液化DMEの添加量を7.5gとし、液化DMEに加えて軽油を添加したこと以外は同じ手順で実験を行ったところ、固体サンプルの含水率は1.0wt%以下となった。
一方、上記の高速液体クロマトグラフの測定の結果、サンプリングした水溶液中のトリオレイン濃度は13ppm、パルミチン酸濃度は14ppmであった。この結果に基づいて、廃油脂モデル溶液から上記固体サンプル中へのトリオレイン及びパルミチン酸の回収率を算出したところ、いずれも99.99%以上であることが分かった。
(result)
As a result of the measurement by the moisture meter, the moisture content of the solid sample was about 2.5 wt% to 3.0 wt%. Compared with the moisture content (20 wt%) of the waste oil model solution before the experiment, the water content was reduced to 1/7 to 1/8, and the waste oil model solution can be efficiently dehydrated by liquefaction extraction with liquefied DME. It became clear. Further, when the experiment was performed in the same procedure except that the temperature of the temperature controller (D) was set to 35 ° C. and the amount of liquefied DME added was 9.75 g, the water content of the solid sample was about 1.4 wt%. Met. Furthermore, when the temperature controller (D) was set to 35 ° C., the amount of liquefied DME added was 7.5 g, and an experiment was performed in the same procedure except that light oil was added in addition to liquefied DME, a solid sample was obtained. The water content was 1.0 wt% or less.
On the other hand, as a result of the measurement by the high performance liquid chromatograph, the triolein concentration in the sampled aqueous solution was 13 ppm, and the palmitic acid concentration was 14 ppm. Based on this result, the recovery rates of triolein and palmitic acid in the solid sample were calculated from the waste oil and fat model solution, and it was found that both were 99.99% or more.

[水及び脂肪酸を高濃度で含有する廃油脂の液化DMEを用いた脱水、並びに、脂肪酸及び油脂の選択的回収 2]
(実験方法)
実施例1の実験において、添加する液化DME量を約11gから約16gに代えたことは同一の方法により実験を行った。液化DME相からサンプリングした固体サンプルの含水率を測定したところ、含水率は3.8wt%であった。
[Dehydration of waste oil containing high concentration of water and fatty acid using liquefied DME and selective recovery of fatty acid and oil 2]
(experimental method)
In the experiment of Example 1, the same method was used to change the amount of liquefied DME to be added from about 11 g to about 16 g. When the moisture content of the solid sample sampled from the liquefied DME phase was measured, the moisture content was 3.8 wt%.

(結果)
この結果と実施例1の結果から、添加する液化DMEの量を多くすればするほど固体サンプルの含水率が低下するというわけではなく、比較的少量を添加することが好ましいことが示された。
(result)
From this result and the result of Example 1, it was shown that the water content of the solid sample does not decrease as the amount of liquefied DME added increases, and it is preferable to add a relatively small amount.

[水及び脂肪酸を高濃度で含有する廃油脂の液化DMEを用いた脱水、並びに、脂肪酸及び油脂の選択的回収 3]
(実験方法)
実施例1の実験で用いた廃油脂モデル溶液に代えて、より含水率の高い廃油脂モデル溶液(トリオレイン6g、パルミチン酸4g、水15gを混合したもの:含水率60wt%)を用い、更に、添加する液化DME量を18.75gから12.4gへと変更したこと以外は、実施例1の実験と同一の方法により実験を行った。
[Dehydration of waste oils and fats containing water and fatty acids at high concentrations using liquefied DME, and selective recovery of fatty acids and oils and fats 3]
(experimental method)
Instead of the waste oil / fat model solution used in the experiment of Example 1, a waste oil / fat model solution having a higher water content (a mixture of 6 g of triolein, 4 g of palmitic acid and 15 g of water: water content of 60 wt%) was further used. The experiment was conducted in the same manner as the experiment in Example 1 except that the amount of liquefied DME to be added was changed from 18.75 g to 12.4 g.

(結果)
液化DME相からサンプリングした固体サンプルの含水率を測定したところ、含水率は3.5wt%であった。一方、水相中のトリオレイン及びパルミチン酸濃度を測定したところ、トリオレイン濃度は32ppm、パルミチン酸濃度は33ppmであった。この結果に基づいて、廃油脂モデル溶液から上記液化DME相へのトリオレイン及びパルミチン酸の回収率を算出したところ、いずれも99.99%以上であることが分かった。 以上の結果から、液化DMEは、含水率60wt%と、かなり含水率が高い廃油脂モデル溶液に対しても、非常に優れた脱水効果を示すと同時に、油脂や脂肪酸の回収率も非常に優れていることが示された。
(result)
When the moisture content of the solid sample sampled from the liquefied DME phase was measured, the moisture content was 3.5 wt%. On the other hand, when the triolein and palmitic acid concentrations in the aqueous phase were measured, the triolein concentration was 32 ppm and the palmitic acid concentration was 33 ppm. Based on this result, the recovery rate of triolein and palmitic acid from the waste oil model solution to the liquefied DME phase was calculated, and it was found that both were 99.99% or more. From the above results, liquefied DME has a water content of 60 wt% and a very high water content of the waste oil and fat model solution. It was shown that.

〔参考例1〕
[廃食用油ゲルの液化DME処理物からのディーゼル燃料の製造]
本発明の脱水処理方法が、ディーゼル燃料(BDF)製造用の原料油脂及び/又は原料脂肪酸の前処理方法として好適であるかを調べるために、図2に示した一連の装置を使用して以下の実験を行った。
[Reference Example 1]
[Production of diesel fuel from liquefied DME treated waste oil gel]
In order to investigate whether the dehydration method of the present invention is suitable as a pretreatment method for raw material fats and / or raw material fatty acids for diesel fuel (BDF) production, a series of apparatuses shown in FIG. The experiment was conducted.

(実験方法)
まず、トリオレイン100mLと、脂肪酸系の食用油固化剤3gとを混合して、廃食用油モデルゲルを調製した。廃食用油モデルゲル15gを、耐圧ガラスセル(A)に添加し、該セルを氷水に浸して、廃食用油モデルゲルを10℃以下程度に冷却した。その後、バルブ(C)を開いて、ガラスシリンダー(B)中の液化DMEをガラスセル(A)内に導入し、液化DMEがガラスセル(A)に約13g程度入ったところでバルブ(C)を閉めた。次に、温度コントローラー(D)の温度を25℃に設定し、ガラスセル(A)内の溶液が設定温度になるまで加熱攪拌した。
(experimental method)
First, 100 mL of triolein and 3 g of a fatty acid-based edible oil solidifying agent were mixed to prepare a waste edible oil model gel. 15 g of waste edible oil model gel was added to the pressure-resistant glass cell (A), the cell was immersed in ice water, and the waste edible oil model gel was cooled to about 10 ° C. or less. Thereafter, the valve (C) is opened, and the liquefied DME in the glass cylinder (B) is introduced into the glass cell (A). When about 13 g of liquefied DME enters the glass cell (A), the valve (C) is opened. Closed. Next, the temperature of the temperature controller (D) was set to 25 ° C., and the mixture was heated and stirred until the solution in the glass cell (A) reached the set temperature.

ガラスセル(A)内の溶液が設定温度に到達した後、攪拌速度を450rpmとして、バルブ(E)を開くとともに、送液ポンプ(F)によって3.5gのKOH含有メタノール溶液をガラスセル(A)内に送液して、エステル交換反応(BDF生成反応)を行った。なお、送液したKOH含有メタノール溶液の量は、そのKOH量が上記トリオレインに対して1wt%の量と固化剤中の脂肪酸を調度中和しうる量との和であり、そのメタノール量が上記トリオレインの6倍モルに相当する量であった。   After the solution in the glass cell (A) reaches the set temperature, the stirring speed is set to 450 rpm, the valve (E) is opened, and 3.5 g of KOH-containing methanol solution is added to the glass cell (A) by the liquid feed pump (F). ) Was fed into the solution and subjected to a transesterification reaction (BDF production reaction). The amount of the KOH-containing methanol solution fed is the sum of the amount of KOH of 1 wt% with respect to the triolein and the amount capable of neutralizing the fatty acid in the solidifying agent. The amount corresponds to 6 moles of the triolein.

上記KOH含有メタノールの送液終了後、すぐにバルブ(G)を開いて、送液ポンプ(H)によって8.9gのメタノールをガラスセル(A)に添加した。それから10分間経過後に、バルブ(I)を開いて、ガラスセル(A)内から液化DMEをDMEガスとして抜いた。その後、ガラスセル(A)内に速やかに1NのHCl水溶液を15mL添加してエステル交換反応を停止させ、次いで、ガラスセル(A)内にテトラヒドロフラン10mLとヘキサン10mLを添加した。ガラスセル(A)内の溶液を15分間ほど攪拌した後、2時間程度静置して相分離し、上相を回収して高速液体クロマトグラフにてトリオレイン(TO)、ジオレイン(DO)、モノオレイン(MO)、及び、BDFの1種であるオレイン酸メチル(OAME)の各濃度を測定した。   Immediately after the feeding of the KOH-containing methanol, the valve (G) was opened, and 8.9 g of methanol was added to the glass cell (A) by the feeding pump (H). After 10 minutes, the valve (I) was opened, and liquefied DME was extracted from the glass cell (A) as DME gas. Thereafter, 15 mL of 1N HCl aqueous solution was quickly added into the glass cell (A) to stop the transesterification reaction, and then 10 mL of tetrahydrofuran and 10 mL of hexane were added into the glass cell (A). After stirring the solution in the glass cell (A) for about 15 minutes, the solution was allowed to stand for about 2 hours to separate the phases, and the upper phase was recovered and triolein (TO), diolein (DO), Each concentration of monoolein (MO) and methyl oleate (OAME) which is one kind of BDF was measured.

(結果)
その結果、上相中のトリオレインは0.0モル%、ジオレインも0.0モル%、モノオレインは1.6モル%、オレイン酸メチルは98.4モル%であった。脂肪酸系の固化剤によってゲル状になった油脂であっても、本発明の脱水処理方法による前処理を行った後、BDF生成反応を行えば、常温という低い温度条件下でも高い反応収率が得られることが示された。
(result)
As a result, triolein in the upper phase was 0.0 mol%, diolein was 0.0 mol%, monoolein was 1.6 mol%, and methyl oleate was 98.4 mol%. Even for fats and oils that have been gelled with a fatty acid-based solidifying agent, a high reaction yield can be achieved even under low temperature conditions of room temperature by performing a BDF formation reaction after pretreatment by the dehydration treatment method of the present invention. It was shown to be obtained.

一方、バルブ(G)からのメタノールの添加を行わず、かつ、上記エステル交換反応(BDF生成反応)の反応時間を15分間としたこと以外は、上記実施例4の実験と同一の方法で実験を行った。上相中のトリオレイン(TO)、ジオレイン(DO)、モノオレイン(MO)、及び、BDFの1種であるオレイン酸メチル(OAME)の各濃度を高速液体クロマトグラフにて測定したところ、トリオレインは4.6モル%、ジオレインは2.4モル%、モノオレインは5.2モル%、オレイン酸メチルは87.8モル%であった。この結果、メタノールをより多く添加すると、BDF生成反応の速度が上昇することがわかった。   On the other hand, the experiment was performed in the same manner as the experiment of Example 4 except that methanol was not added from the valve (G) and the reaction time of the transesterification reaction (BDF generation reaction) was 15 minutes. Went. When each concentration of triolein (TO), diolein (DO), monoolein (MO), and methyl oleate (OAME), which is one type of BDF, was measured with a high performance liquid chromatograph, Rein was 4.6 mol%, diolein was 2.4 mol%, monoolein was 5.2 mol%, and methyl oleate was 87.8 mol%. As a result, it was found that when more methanol was added, the rate of the BDF production reaction was increased.

水及び脂肪酸を高濃度で含有する廃油脂の液化DMEを用いた脱水、並びに、脂肪酸及び油脂の選択的回収実験に用いた実験装置を示す図である。図1中の各符号はそれぞれ以下のものを示す。A:耐圧セル、B:ガラスシリンダー(液化DME)、C:バルブ、D:コントローラー(温度及び回転数)、E:バルブ、F:液化DME相回収ライン、G:サンプルびん、H:バルブ、I:水相回収ライン、J:サンプルびん、K:攪拌モーター、L:熱電対、M:攪拌翼、N:バルブIt is a figure which shows the experimental apparatus used for the spin-drying | dehydration using the liquefied DME of the waste oil and fat containing water and a fatty acid at high concentration, and the selective collection | recovery experiment of a fatty acid and fat. Each symbol in FIG. 1 indicates the following. A: pressure cell, B: glass cylinder (liquefied DME), C: valve, D: controller (temperature and rotation speed), E: valve, F: liquefied DME phase recovery line, G: sample bottle, H: valve, I : Water phase recovery line, J: sample bottle, K: stirring motor, L: thermocouple, M: stirring blade, N: valve 廃食用油ゲルの液化DME処理物からのディーゼル燃料の製造実験に用いた実験装置を示す図である。図2中の各符号はそれぞれ以下のものを示す。A:耐圧セル、B:ガラスシリンダー(液化DME)、C:バルブ、D:コントローラー(温度及び回転数)、E:バルブ、F:送液ポンプ、G:バルブ、H:送液ポンプ、I:バルブ、J:攪拌モーター、K:攪拌翼、L:熱電対、M:KOH含有メタノール溶液、N:メタノールIt is a figure which shows the experimental apparatus used for the manufacture experiment of the diesel fuel from the liquefied DME processed material of waste edible oil gel. Each symbol in FIG. 2 indicates the following. A: pressure cell, B: glass cylinder (liquefied DME), C: valve, D: controller (temperature and rotation speed), E: valve, F: liquid pump, G: valve, H: liquid pump, I: Valve, J: stirring motor, K: stirring blade, L: thermocouple, M: methanol solution containing KOH, N: methanol

Claims (11)

水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル溶液として、選択的に脱水、回収することを特徴とする水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法。 Water, fatty acids and / or water and / or fatty acids and / or fats and / or oils are added to a substance containing water and fatty acids and / or fats and oils as an extraction solvent, and the fatty acids and / or fats and oils are selectively dehydrated and recovered as liquefied dimethyl ether solutions. Alternatively, a method for selective dehydration and recovery of fatty acids and / or fats and oils from substances containing fats and oils. 水と脂肪酸及び/又は油脂とを含む物質が、水を含有する食用油脂類、水及び/又は非油脂類を含有する廃食用油脂類或いは廃食用油脂類以外の廃油脂類であることを特徴とする請求項1記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法。 The substance containing water and fatty acids and / or fats and oils is edible fats and oils containing water, waste edible fats and oils containing water and / or non-fats or waste fats and oils other than waste edible fats and oils The method for selectively dehydrating and recovering fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils according to claim 1. 水と脂肪酸及び/又は油脂とを含む物質が、泥状又はゲル状の脂肪酸及び/又は油脂の固形物を含有していることを特徴とする請求項1又は2記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法。 The substance containing water and fatty acid and / or fat / oil contains a solid matter of mud or gel-like fatty acid and / or fat / oil, according to claim 1 or 2, A method for selective dehydration and recovery of fatty acids and / or fats and oils from substances containing fats and oils. 水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加、攪拌して、液相の均一相を形成し、その後静置して、液化ジメチルエーテル相と水相との二液相を形成させ、該相より液化ジメチルエーテル相を分離することよりなる請求項1〜3のいずれか記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法。 Add liquefied dimethyl ether as an extraction solvent to a substance containing water and fatty acids and / or fats and oils, stir to form a uniform liquid phase, and then let stand, then two liquids of liquefied dimethyl ether phase and aqueous phase Selective dehydration of fatty acids and / or fats from substances containing water and fatty acids and / or fats and oils according to any one of claims 1 to 3, comprising forming a phase and separating a liquefied dimethyl ether phase from the phase Collection method. 水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル溶液として、選択的に脱水、回収するに際し、抽出溶媒に軽油成分を添加することを特徴とする請求項1〜4のいずれか記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法。 Add liquefied dimethyl ether as an extraction solvent to substances containing water and fatty acids and / or fats and oils, and add light oil components to the extraction solvent when selectively dehydrating and collecting fatty acids and / or fats and oils as liquefied dimethyl ether solutions. The method for selectively dehydrating and recovering fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils according to any one of claims 1 to 4. 軽油成分の添加が、抽出処理液全量に対して、10〜50容量%の範囲で添加されることを特徴とする請求項5記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法。 The addition of the light oil component is added in a range of 10 to 50% by volume with respect to the total amount of the extraction treatment liquid, and the fatty acid from the substance containing water and the fatty acid and / or oil and fat according to claim 5 and // Selective dehydration / recovery method of fats and oils. 水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル溶液として、選択的に脱水、回収する処理を、温度10〜35℃の範囲で行なうことを特徴とする請求項1〜6のいずれか記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法。 A process in which liquefied dimethyl ether is added as an extraction solvent to a substance containing water and fatty acids and / or fats and oils, and the fatty acid and / or fats and oils are selectively dehydrated and recovered as a liquefied dimethyl ether solution within a temperature range of 10 to 35 ° C. The method for selective dehydration / recovery of fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils according to any one of claims 1 to 6. 水と脂肪酸及び/又は油脂とを含む物質に、液化ジメチルエーテルを抽出溶媒として添加し、脂肪酸及び/又は油脂を液化ジメチルエーテル溶液として、選択的に脱水、回収する処理を、温度30〜35℃の範囲に調整して行なうことを特徴とする請求項7記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法。 A process in which liquefied dimethyl ether is added as an extraction solvent to a substance containing water and fatty acids and / or fats and oils, and the fatty acid and / or fats and oils are selectively dehydrated and recovered as a liquefied dimethyl ether solution within a temperature range of 30 to 35 ° C. The method for selective dehydration and recovery of fatty acids and / or fats and oils from substances containing water and fatty acids and / or fats and oils according to claim 7, wherein 請求項1〜8のいずれか記載の水と脂肪酸及び/又は油脂とを含む物質からの脂肪酸及び/又は油脂の選択的脱水・回収方法により、脱水された脂肪酸及び/又は油脂と、液化ジメチルエーテルとを含む物質を調製することを特徴とする、バイオディーゼル燃料製造のための原料油の調製方法。 Fatty acid and / or oil and fat dehydrated by a method for selectively dehydrating and recovering fatty acid and / or fat from a substance containing water and fatty acid and / or fat according to any one of claims 1 to 8, and liquefied dimethyl ether A method for preparing a feedstock for biodiesel fuel production, comprising preparing a substance containing バイオディーゼル燃料の製造が、液化ジメチルエーテルを添加した均一相系でのエステル交換反応を行なう方法によるものであることを特徴とする請求項9記載のバイオディーゼル燃料製造のための原料油の調製方法。 The method for preparing a feedstock for biodiesel fuel production according to claim 9, wherein the biodiesel fuel is produced by a method of performing a transesterification reaction in a homogeneous phase system to which liquefied dimethyl ether is added. バイオディーゼル燃料製造のための原料油の調製が、酸触媒、低級アルコールを用いた遊離脂肪酸のエステル化反応と併用して行なわれることを特徴とする請求項9又は10記載のバイオディーゼル燃料製造のための原料油の調製方法。 The biodiesel fuel production process according to claim 9 or 10, wherein the preparation of the raw material oil for biodiesel fuel production is carried out in combination with an esterification reaction of free fatty acid using an acid catalyst and a lower alcohol. For preparing raw material oils for
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012035213A (en) * 2010-08-09 2012-02-23 Central Res Inst Of Electric Power Ind Method for treating deposit, and extracting apparatus
KR101263984B1 (en) 2009-12-24 2013-05-13 정규백 Manufacturing method for fatty acid methyl ester by using neutural catalyst
JP2014108408A (en) * 2012-12-03 2014-06-12 Mitsubishi Heavy Ind Ltd Dehydration treatment apparatus for pcb contaminated sludge or residues, and pcb processing system using the same
CN107794117A (en) * 2016-09-06 2018-03-13 湖南省林业科学院 A kind of based polar adjustable type vegetable fat solvent acid stripping method of alcohol
WO2019078172A1 (en) * 2017-10-19 2019-04-25 公立大学法人大阪府立大学 Method for processing oils and fats containing free fatty acid and oil content

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101263984B1 (en) 2009-12-24 2013-05-13 정규백 Manufacturing method for fatty acid methyl ester by using neutural catalyst
JP2012035213A (en) * 2010-08-09 2012-02-23 Central Res Inst Of Electric Power Ind Method for treating deposit, and extracting apparatus
JP2014108408A (en) * 2012-12-03 2014-06-12 Mitsubishi Heavy Ind Ltd Dehydration treatment apparatus for pcb contaminated sludge or residues, and pcb processing system using the same
CN107794117A (en) * 2016-09-06 2018-03-13 湖南省林业科学院 A kind of based polar adjustable type vegetable fat solvent acid stripping method of alcohol
WO2019078172A1 (en) * 2017-10-19 2019-04-25 公立大学法人大阪府立大学 Method for processing oils and fats containing free fatty acid and oil content

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