JP2001089753A - Oil-treating agent - Google Patents

Oil-treating agent

Info

Publication number
JP2001089753A
JP2001089753A JP5539998A JP5539998A JP2001089753A JP 2001089753 A JP2001089753 A JP 2001089753A JP 5539998 A JP5539998 A JP 5539998A JP 5539998 A JP5539998 A JP 5539998A JP 2001089753 A JP2001089753 A JP 2001089753A
Authority
JP
Japan
Prior art keywords
oil
dispersant
oils
alkali
phase
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP5539998A
Other languages
Japanese (ja)
Other versions
JP3564292B2 (en
Inventor
Kunimitsu Tamura
邦光 田村
Tatsuo Kasahara
達男 笠原
Tomohiro Shiitani
智洋 椎谷
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
PURESUTO KK
Hakugen Co Ltd
Original Assignee
PURESUTO KK
Hakugen Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by PURESUTO KK, Hakugen Co Ltd filed Critical PURESUTO KK
Priority to JP5539998A priority Critical patent/JP3564292B2/en
Priority to PCT/JP1999/001015 priority patent/WO1999045086A1/en
Priority to AU27452/99A priority patent/AU2745299A/en
Publication of JP2001089753A publication Critical patent/JP2001089753A/en
Application granted granted Critical
Publication of JP3564292B2 publication Critical patent/JP3564292B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B15/00Solidifying fatty oils, fats, or waxes by physical processes
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B13/00Recovery of fats, fatty oils or fatty acids from waste materials
    • 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
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/74Recovery of fats, fatty oils, fatty acids or other fatty substances, e.g. lanolin or waxes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Fats And Perfumes (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a oil-treating agent capable of treating waste oil to solidify the oil at a temperature near ambient temperature, capable of being easily mixed with the waste oil, and decreasing the amount of strong alkali to be used therewith. SOLUTION: This oil-treating agent comprises a water-in-oil(W/O) type emulsion formed by dispersing an aqueous dispersed phase in an oily continuous phase, wherein the dispersed phase comprises water, a solution containing water and an alcohol, and an alkali-mixed solution which is formed by mixing an water-free alcohol with an alkali hydroxide, such as sodium hydroxide, or with an alkali metal alkoxide, such as sodium alkoxide, and the continuous phase comprises a liquid not compatible with the dispersed phase.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は油処理剤に係り、詳しく
は家庭用のてんぷら油や業務用の食用廃油などを処理す
るために用いられる油を凝固する油処理剤に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an oil dispersant, and more particularly, to an oil dispersant which coagulates oil used for treating home-use tempura oil and commercial edible waste oil.

【0002】[0002]

【従来の技術】従来、使用済みのてんぷら油や業務用の
食用廃油(以下、廃油という)を処理するために、低分
子のポリエチレンやパラフィン等を廃油に投入し、凝固
させ廃棄していた。また、特公昭60-054092号公報に記
載の発明では、12-ヒドロキシステアリン酸を廃食用油
に適量添加し、水を共存せしめることなく加熱溶解後、
冷却する廃食用油の固形化処理方法を提案している。ま
た、特開平9-013072号公報に記載の発明では、常温で液
状の油脂を水酸化ナトリウム、水酸化カリウムの様なア
ルカリで鹸化する場合完全鹸化に要するアルカリの量の
1/6〜1/3で鹸化し、その鹸化開始後約1〜3分で固化す
るための溶液型(均一系)の鹸化促進剤を提案してい
る。
2. Description of the Related Art Conventionally, in order to treat used tempura oil and commercial edible waste oil (hereinafter referred to as waste oil), low-molecular-weight polyethylene, paraffin and the like have been introduced into waste oil, coagulated and discarded. Further, in the invention described in Japanese Patent Publication No. 60-054092, an appropriate amount of 12-hydroxystearic acid is added to waste cooking oil, and after heating and dissolving without allowing water to coexist,
A method of solidifying waste cooking oil to be cooled has been proposed. Further, in the invention described in JP-A-9-013072, the amount of the alkali required for complete saponification when saponifying liquid oils and fats at room temperature with an alkali such as sodium hydroxide and potassium hydroxide.
A solution type (homogeneous) saponification accelerator for saponifying at 1/6 to 1/3 and solidifying about 1 to 3 minutes after the start of saponification has been proposed.

【0003】[0003]

【本発明が解決しようとする課題】このため、低分子の
ポリエチレンやパラフィン等を用いたものであると廃油
が高温のうちに添加しないと凝固しないという問題があ
った。また、特公昭60-054092号公報に記載の発明で
は、廃油が高温のうちに添加しないと凝固しないという
問題があり、冷めてしまった油を処理するには加熱しな
ければならなかった。さらに、廃油の温度が室温付近に
下がって初めて廃油が固形化するため時間と手間がかか
るという問題があった。
For this reason, when low molecular polyethylene or paraffin is used, waste oil does not solidify unless it is added at high temperature. Also, the invention described in Japanese Patent Publication No. Sho 60-054092 has a problem that the waste oil does not solidify unless it is added at a high temperature, so that it has to be heated to treat the cooled oil. Further, there is a problem that it takes time and effort since the waste oil is solidified only after the temperature of the waste oil drops to around room temperature.

【0004】また、特開平9-013072号公報に記載の発明
では、常温から90℃ぐらいの間で廃油を凝固させるこ
とができるが、均一な溶液であるのでこの鹸化促進剤と
廃油との接触面積が小さく、また、廃油との相溶性が低
いため混ざりにくく撹拌する手間が大きかった。さらに
また、混ざりにくく鹸化反応が進みにくいために過剰の
強アルカリを使用しなければならず、その腐食性を有す
る強アルカリが使用の際に人体に接触すると、皮膚を損
傷する恐れがあり、あまり好ましくない。また、強アル
カリの腐食性は、金属も侵す恐れがあるため、てんぷら
鍋などの調理具を腐食する恐れがあり好ましくない。
In the invention described in Japanese Patent Application Laid-Open No. 9-013072, waste oil can be coagulated between room temperature and about 90 ° C. However, since it is a uniform solution, the contact between the saponification accelerator and the waste oil can be prevented. Since the area was small and the compatibility with the waste oil was low, it was hard to mix and the trouble of stirring was large. Furthermore, since the mixture is hard to mix and the saponification reaction hardly proceeds, an excessive strong alkali must be used, and if the corrosive strong alkali comes into contact with the human body during use, the skin may be damaged, and Not preferred. In addition, since the corrosiveness of the strong alkali may involve metal, the cooking utensils such as tempura pots may be corroded, which is not preferable.

【0005】本発明者らは、上記課題を解決するため鋭
意研究の結果、次の事項に着目し解決できることを見い
だした。W/O型エマルションの油処理剤で、エマルショ
ン中の分散相の粒子径が15μmかそれ以下の粒子であっ
て、粒子中に高濃度の水酸化ナトリウム等のアルカリ溶
液を閉じこめ、他方、連続相はエマルション中の粒子と
混ざらない液体を使用することで、高濃度のアルカリ溶
液を無数の微小な粒子に閉じこめることができ、廃油に
加え撹拌したとき廃油と無数の微小粒子となったアルカ
リ溶液の接触面積が非常に大きくなるため、鹸化反応が
全体として速く進行し、短時間で固化させることができ
ることを見いだした。このとき、前記エマルションの粒
子を、連続相との界面において界面活性剤の吸着によっ
て形成される膨潤ミセルにより液中に小粒子で安定して
分散させることもできる。
The inventors of the present invention have conducted intensive studies to solve the above-mentioned problems, and have found that the following problems can be solved by focusing on the following items. An oil dispersant for a W / O emulsion, in which the particle size of the dispersed phase in the emulsion is 15 μm or less, and the high-concentration alkaline solution such as sodium hydroxide is trapped in the particles. By using a liquid that does not mix with the particles in the emulsion, high-concentration alkaline solution can be confined to countless fine particles. Since the contact area becomes very large, it has been found that the saponification reaction proceeds rapidly as a whole and can be solidified in a short time. At this time, the emulsion particles can be stably dispersed in the liquid as small particles by swelling micelles formed by adsorption of a surfactant at the interface with the continuous phase.

【0006】食用油等は化学構造的には基本的に脂肪酸
とグリセリンの脂肪酸エステルであることが知られてい
る。これに水酸化ナトリウム等のアルカリを加えて反応
させると鹸化反応により脂肪酸ソーダすなわち石鹸が精
製し固化する。石鹸を製造する場合は通常、エステルを
完全に鹸化するに要する苛性アルカリを必要とする。本
発明は、基本的には苛性アルカリを食用油に加えること
によって石鹸精製による固化現象を利用して廃油を固化
するのが目的である。
[0006] It is known that edible oils and the like are basically fatty acid esters of fatty acids and glycerin in chemical structure. When an alkali such as sodium hydroxide is added thereto and reacted, a fatty acid soda, that is, a soap is purified and solidified by a saponification reaction. The manufacture of soap usually requires the caustic required to completely saponify the ester. An object of the present invention is to basically solidify waste oil by adding a caustic alkali to edible oil and utilizing a solidification phenomenon by soap refining.

【0007】すなわちすべての廃油を鹸化する必要はな
く部分鹸化で足りる。すなわち部分鹸化で固化が達成さ
れれば十分である。(石鹸を製造することと異なる点は
固化が目的であって、100%完全に鹸化する必要はな
い。)このような目的で従来から溶液型すなわち例えば
水酸化ナトリウムを水−アルコ−ル類等をベース基材に
溶解した均一系溶液の固化剤が検討されてきたが、本発
明者らは溶液型固化剤においては一定量の固化処理剤で
廃油を実用的な固さにまで固化するためには高濃度のア
ルカリ溶液とする必要があることを確認した。すなわち
廃油と油処理剤の反応性が悪いために高濃度のアルカリ
溶液を過剰量必要とするわけである。さらにこの溶液型
の高濃度アルカリ溶液固化処理剤の欠点として、アルカ
リ濃度が高いため皮膚接触時における安全性の問題やて
んぷら鍋などの調理具に対する腐食性の問題も考えられ
る。また、溶液型で低濃度アルカリ溶液の処理剤の固化
能力を調べた結果、固化が不十分であるある事が分かっ
た。
That is, it is not necessary to saponify all waste oils, and partial saponification is sufficient. That is, it is sufficient if solidification is achieved by partial saponification. (The difference from producing soap is for the purpose of solidification, and it is not necessary to completely saponify it.) For such purpose, a solution type, for example, sodium hydroxide and water-alcohols are conventionally used. Although a solidifying agent of a homogeneous solution in which is dissolved in a base material has been studied, the present inventors have found that in a solution type solidifying agent, a certain amount of solidifying agent solidifies waste oil to a practical hardness. It was confirmed that a high concentration alkaline solution was required. That is, since the reactivity between the waste oil and the dispersant is poor, an excessive amount of a high-concentration alkaline solution is required. Further, as a drawback of the solution-type high-concentration alkali solution solidifying agent, there may be a problem of safety at the time of skin contact due to a high alkali concentration and a problem of corrosiveness to cooking utensils such as a tempura pan. In addition, as a result of examining the solidification ability of the treating agent for a low-concentration alkaline solution in a solution type, it was found that the solidification was insufficient.

【0008】そこで、本発明者らは、これらの原因につ
いて鋭意研究した結果、従来の溶液型固化処理剤におい
ては、全体が均一な液体であるので、これをてんぷら鍋
等の容器中の食用油に混合した場合、主婦あるいは作業
員等による菜箸、へら等による人為的な攪拌では処理剤
と食用油との混合が十分に行われずアルカリ溶液とてん
ぷら油との接触面積が小さくそのために鹸化の反応速度
が小さいと推察した。これを解決するために従来ではア
ルカリの量を過剰に加えるか、濃度を過剰に高くする必
要があった。(例えば、処理剤全体に対して20〜40
%の高濃度)つまり、従来技術の溶液型の油処理剤で
は、はじめからほぼ均一な液体であるのでアルカリ溶液
と食用油などの廃油との接触は、油処理剤添加後の撹拌
のみによって行われるため廃油中で粒子にあるアルカリ
成分の粒子径が大きく、そのためにアルカリ溶液と廃油
との接触面積が小さい。一方、本発明のようなW/O型エ
マルションとした場合、はじめからアルカリ溶液を微小
粒子で分散させているため、少しの撹拌で廃油とアルカ
リ溶液との大きな接触面積を確保することができる。
The inventors of the present invention have conducted intensive studies on these causes, and found that the conventional solution-type solidifying agent is a uniform liquid as a whole, and is therefore used as an edible oil in a container such as a tempura pan. When mixed artificially with chopsticks, spatula etc. by housewife or worker, the treatment agent and edible oil are not sufficiently mixed and the contact area between the alkaline solution and the tempura oil is small, so the saponification reaction I speculated that the speed was small. In order to solve this, conventionally, it has been necessary to add an excessive amount of alkali or excessively increase the concentration. (For example, 20 to 40 with respect to the entire treatment agent)
In other words, in the case of the solution type dispersant of the related art, since the liquid is almost uniform from the beginning, the contact between the alkaline solution and the waste oil such as edible oil is performed only by stirring after the dispersant is added. Therefore, the particle diameter of the alkali component in the particles in the waste oil is large, and therefore, the contact area between the alkaline solution and the waste oil is small. On the other hand, in the case of the W / O emulsion as in the present invention, since the alkali solution is dispersed in the form of fine particles from the beginning, a large contact area between the waste oil and the alkali solution can be secured with a little stirring.

【0009】本発明のエマルション型の油処理剤では、
アルカリをW/O型エマルションの液滴中に閉じこめたも
のであるので、処理剤中のアルカリ濃度を下げても十分
な固化性能が得られることを見いだし、廃油に本発明の
油処理剤を用いると、微少なアルカリ溶液の粒子が分散
し廃油との接触面積が従来の油処理剤に比べ飛躍的に増
大し、鹸化の反応速度が増大する。よって、アルカリの
使用量を低減することも可能となり、使用者が油処理剤
に接触した際や、廃油を入れた調理器具を損傷するおそ
れが低減される。
In the emulsion type dispersant of the present invention,
Since the alkali is confined in the droplets of the W / O emulsion, it has been found that sufficient solidification performance can be obtained even when the alkali concentration in the treating agent is reduced, and the oil treating agent of the present invention is used for waste oil. Then, the fine alkaline solution particles are dispersed and the contact area with the waste oil is dramatically increased as compared with the conventional dispersant, so that the saponification reaction rate is increased. Therefore, it is also possible to reduce the amount of alkali used, and it is possible to reduce the possibility that the user may come into contact with the dispersant or damage cooking utensils containing waste oil.

【0010】本発明は以上のような従来の欠点に鑑み、
廃油を常温付近でも固化させることができ、廃油と混ざ
りやすく、強アルカリの使用量を低減することのできる
油処理剤を提供することを目的としている。
The present invention has been made in view of the above-mentioned conventional drawbacks,
It is an object of the present invention to provide an oil treating agent which can solidify waste oil even at around normal temperature, is easily mixed with waste oil, and can reduce the amount of strong alkali used.

【0011】[0011]

【課題を解決するための手段】上記目的を達成するため
に、アルカリの水/アルコ−ル溶液をこれと相溶性の無
いまたは相溶性の小さい溶液と混合・攪拌し、油中水滴
型(W/O型)エマルションである油処理剤を提供するこ
とを要旨としている。
In order to achieve the above object, an alkali water / alcohol solution is mixed and stirred with a solution having no or little compatibility with the solution, and a water-in-oil type (W) is used. The main point is to provide an oil dispersant which is an emulsion.

【0012】本発明に用いられるW/O型エマルションと
して、分散相としては、アルカリを混合した溶液が用い
られる。また、連続相としては、分散相の成分と互いに
溶解し合わない(すなわち相溶性のないまたは小さい)
液体基材である必要がある。さらに、好ましくは、廃油
と混ざりやすいことにより固化速度を上げられるため、
鉱物油や合成油などのいわゆるオイルが用いられる。
In the W / O emulsion used in the present invention, a solution in which an alkali is mixed is used as a dispersed phase. In addition, as a continuous phase, the components of the dispersed phase do not dissolve in each other (that is, they are incompatible or small).
It must be a liquid substrate. Further, preferably, since the solidification rate can be increased by being easily mixed with the waste oil,
So-called oils such as mineral oils and synthetic oils are used.

【0013】すなわち、本発明に用いられる連続相の好
ましい例としては、鉱物油、合成油が好ましく、1種ま
たは2種以上を混合して用いることもでき、鉱物油では
高度に精製したホワイトオイルを用いても良い。例え
ば、鉱物油である潤滑油基油のスピンドル油、トランス
油、ニュートラル油、ブライトストック油や、燃料油の
石油ナフサ、ガソリン、灯油、軽油や、プロセスオイル
や、合成油である合成系エステル油や合成系エ−テル
油、合成系ポリアルキレングリコール油、合成系ポリア
ルファオレフィン、アルキルベンゼン油、シリコンオイ
ルなどが挙げられる。
That is, as a preferred example of the continuous phase used in the present invention, mineral oil and synthetic oil are preferred, and one or a mixture of two or more thereof can be used. May be used. For example, mineral oils such as spindle oils of lubricating base oils, transformer oils, neutral oils, bright stock oils, petroleum naphthas as fuel oils, gasoline, kerosene, light oils, process oils, and synthetic ester oils as synthetic oils And synthetic ether oils, synthetic polyalkylene glycol oils, synthetic polyalphaolefins, alkylbenzene oils, silicone oils and the like.

【0014】さらに、本発明に用いられる連続相のW/O
エマルション全体に対する連続相の比としては、特に制
限はないが、40〜95%程度の連続相を用いるのが好
ましい。
Further, the W / O of the continuous phase used in the present invention
The ratio of the continuous phase to the whole emulsion is not particularly limited, but it is preferable to use a continuous phase of about 40 to 95%.

【0015】また、本発明に用いられる分散相の中のア
ルカリ成分と混合する水または水とアルコール、あるい
はアルコールの比率としては、特に制限はないがアルカ
リ成分:水:アルコール=3:3:7が特に好ましい。
There is no particular limitation on the water to be mixed with the alkali component in the disperse phase used in the present invention, or the ratio of water to alcohol or the alcohol, but alkali component: water: alcohol = 3: 3: 7. Is particularly preferred.

【0016】本発明に用いられるアルカリとしては、強
アルカリであれば特に制限はないが、水酸化ナトリウ
ム、水酸化カリウム、水酸化リチウム、水酸化バリウム
等が用いられる。好ましくは、水酸化ナトリウムが用い
られる。
The alkali used in the present invention is not particularly limited as long as it is a strong alkali, and sodium hydroxide, potassium hydroxide, lithium hydroxide, barium hydroxide and the like are used. Preferably, sodium hydroxide is used.

【0017】また、本発明に用いられる金属アルコキシ
ドとしては、ナトリウムアルコキシドが好ましく、ナト
リウムエトキシド、ナトリウムメトキシドまたはそれら
の混合物が用いられる。
The metal alkoxide used in the present invention is preferably a sodium alkoxide, and sodium ethoxide, sodium methoxide or a mixture thereof is used.

【0018】本発明に用いられる分散相のアルカリ溶液
のアルカリ濃度としては、3〜60%程度の高濃度が好
ましく、さらに好ましくは30%程度の濃度が用いられ
る。また、水とアルコールの比率としては、特に制限は
ないが、水:アルコール=20〜40:60〜80程度
が好ましい。
The alkali concentration of the alkali solution of the dispersed phase used in the present invention is preferably as high as about 3 to 60%, more preferably about 30%. The ratio of water to alcohol is not particularly limited, but water: alcohol = 20 to 40:60 to 80 is preferable.

【0019】また、本発明に用いられる分散相としての
アルカリ混合溶液の粒子径は、特に制限はなく、15μm
以下のものが用いられ、好ましくは10μm以下、さら
に好ましくは3μm以下のものがよい。粒子径が大きい
と反応性が低下し、また、エマルションとしての分散安
定性が悪くなる。
The particle size of the alkali mixed solution as the disperse phase used in the present invention is not particularly limited, and is 15 μm
The following are used, preferably 10 μm or less, more preferably 3 μm or less. If the particle size is large, the reactivity is reduced, and the dispersion stability as an emulsion is deteriorated.

【0020】油処理剤の成分として増量またはアルカリ
濃度の希釈のため粉体を用いることも否定するものでは
なく、例えば、他に水酸化カルシウム、硫酸カルシウ
ム、ベントナイト、カオリナイト、パーライトあるいは
カーボンブラック、活性炭等の炭素状粒子などを混合し
ても良い。
The use of powder for increasing the amount or diluting the alkali concentration as a component of the dispersant is not denied. For example, calcium hydroxide, calcium sulfate, bentonite, kaolinite, pearlite or carbon black, Carbonaceous particles such as activated carbon may be mixed.

【0021】また、本発明の油処理剤として用いるW/O
エマルションを形成するために、好ましくはアルカリ混
合溶液をオイル分に分散させる分散剤として界面活性剤
を用いることができる。なお、分散剤を用いない場合
は、使用時(廃油に本発明の油処理剤を添加する直前
に)に油処理剤を強く撹拌してから、廃油に添加すれば
よい。例えば、本発明の油処理剤が1回の使用量ごとに
ボトルに充填したタイプのものであれば、そのボトルご
と振れば撹拌する手間はそれ程かからず好ましい。
The W / O used as the dispersant of the present invention
In order to form an emulsion, a surfactant can be preferably used as a dispersant for dispersing an alkali mixed solution in an oil component. When the dispersant is not used, the dispersant may be added to the waste oil after being strongly stirred at the time of use (immediately before the dispersant of the present invention is added to the waste oil). For example, if the dispersant of the present invention is of a type in which a bottle is filled for each use amount, shaking the entire bottle is preferable because it does not take much time for stirring.

【0022】本発明に用いられる界面活性剤としては、
連続相中に分散相を長い間安定して分散されておくこと
ができれば、特に制限はないが連続相であるオイル分の
性質や分散相の濃度等を考慮し、種類、使用量を適宜調
整すればよく、例えば、ポリアルケニル琥珀酸イミド、
またはその誘導体、ポリアルケニル琥珀酸アミド、また
はその誘導体、ポリオレフィンアミド系またはその誘導
体、アルキル/アルケニルアミン系、またはその誘導
体、ポリオレフィンアミドアルケンアミン系またはその
誘導体、ポリオキシエチレン系、ポリオキシフェニルエ
ーテル系、アルカリ金属およびアルカリ土類金属石鹸系
の界面活性剤を1種または2種以上を用いることができ
る。
The surfactant used in the present invention includes:
There is no particular limitation as long as the dispersed phase can be stably dispersed in the continuous phase for a long time, but the type and amount of use are appropriately adjusted in consideration of the properties of the oil component that is the continuous phase and the concentration of the dispersed phase. For example, polyalkenyl succinimide,
Or a derivative thereof, a polyalkenyl succinamide or a derivative thereof, a polyolefin amide or a derivative thereof, an alkyl / alkenylamine system or a derivative thereof, a polyolefin amide alkene amine or a derivative thereof, a polyoxyethylene system, and a polyoxyphenyl ether system. One or more alkali metal and alkaline earth metal soap-based surfactants can be used.

【0023】[0023]

【作用】廃油に添加された本発明の油処理剤は、W/O型
エマルションとしたので、微少で無数のアルカリの粒子
が廃油中に分散し、鹸化の反応が始まる。微少で無数の
アルカリの液滴としたことで廃油とアルカリ溶液の接触
面積が増大したため、速やかに固化し廃油を処理でき
る。
Since the dispersant of the present invention added to the waste oil is a W / O emulsion, minute and innumerable alkali particles are dispersed in the waste oil, and the saponification reaction starts. Since the contact area between the waste oil and the alkali solution is increased by forming minute and innumerable alkali droplets, the waste oil can be rapidly solidified and treated.

【0024】上記のように構成された油処理剤は、ま
ず、家庭で使用したてんぷら油を処理する際は、常温付
近の廃油に本発明の油処理剤を添加し、撹拌する。する
と、すぐに廃油と油処理剤が反応を始め、およそ1分ほ
どで固化するので鍋から剥離して廃棄することができ
る。
When the dispersant configured as described above is used to treat tempura oil used at home, first, the dispersant of the present invention is added to waste oil at around normal temperature and stirred. Then, the waste oil and the dispersant immediately start reacting and solidify in about one minute, so that the waste oil can be peeled off from the pot and discarded.

【0025】[0025]

【実施例】以下、本発明の実施例を説明するが、本発明
は実施例に限定されるものではない。
Embodiments of the present invention will be described below, but the present invention is not limited to the embodiments.

【0026】なお、実施例においては、4つの評価試験
法用いて本発明による油処理剤と従来技術による油処理
剤の性能の比較結果を説明する。
In the examples, the results of comparison of the performance of the dispersant according to the present invention and the conventional dispersant will be described using four evaluation test methods.

【0027】[評価試験法1]市販のガラスビーカーと
磁気式撹拌機(マグネットスターラー)を使用する。使
用した磁気式撹拌機は撹拌子の回転数がLED表示で直読
できるものを用いた。(型式;井内誠栄堂モデル番号HS
-500出力100V,0.5A)この磁気式撹拌機によれば、ビー
カー中の内容物が固化を始めると粘度が増加し、撹拌子
の負荷が増大することによって回転数が低下する。固化
の程度により回転数の低下の度合いが異なり、固く固化
するほど回転数は低くなる。言い換えると、回転数の低
下の状況を観察することによって固化の程度が確認でき
るものである。
[Evaluation Test Method 1] A commercially available glass beaker and a magnetic stirrer (magnet stirrer) are used. The magnetic stirrer used was one in which the number of revolutions of the stirrer could be read directly by LED display. (Model: Inuchi Seieido Model Number HS
According to this magnetic stirrer, when the contents in the beaker start to solidify, the viscosity increases, and the load on the stirrer increases, so that the rotation speed decreases. Depending on the degree of solidification, the degree of decrease in the number of rotations differs, and the more solidified the lower the number of rotations. In other words, the degree of solidification can be confirmed by observing the state of the decrease in the number of revolutions.

【0028】試験においては、まず、100mlのパイレッ
クスガラス製ビーカー中に食用油の廃油50mlを入れる。
テフロンコーティングをした磁気撹拌子をこの中に入れ
室温にて撹拌する。油処理剤を入れる前にこの回転数を
450rpm±10rpmに設定しておく。次に、試験用油処理剤
をビーカー中に加え、直ちに撹拌子の回転数を読みその
経時変化を観測記録する。
In the test, first, 50 ml of edible oil waste oil is placed in a 100 ml Pyrex glass beaker.
A magnetic stirrer coated with Teflon is put into this and stirred at room temperature. Before putting in the dispersant,
Set to 450rpm ± 10rpm. Next, the test dispersant is added into a beaker, and the rotation speed of the stirrer is immediately read to observe and record the change over time.

【0029】本試験法によれば、固化性能の優れた油処
理剤は短時間で固化が起こるため回転数が急激に低下す
る。固化の判断基準を20rpm(1分間に20回転)と
し、固化に要するアルカリ(水酸化ナトリウム)換算の
必要量、及び固化時間を求めた。
According to this test method, the dispersant having excellent solidification performance rapidly solidifies because the solidification occurs in a short time. The criterion for solidification was 20 rpm (20 rotations per minute), and the required amount of alkali (sodium hydroxide) required for solidification and the solidification time were determined.

【0030】[評価試験法2]室温にててんぷら鍋中に
てんぷら油の廃油600ml(室温)を入れる。油処理剤100
mlを加え直ちに、菜箸で1分間よく撹拌しその後放置す
る。この間、固化開始までの時間、固化に要した時間を
測定する。(てんぷら鍋の大きさは直径約 27cmφ、
深さ約 5cm)本試験法によれば、所定量のてんぷら油
を固化するに要するアルカリ(水酸化ナトリウム)の量
を求め、本発明による油処理剤と従来技術による油処理
剤の違いを評価する。
[Evaluation Test Method 2] 600 ml (room temperature) of waste oil of tempura oil is put in a tempura pan at room temperature. Dispersant 100
Immediately after adding ml, stir well with chopsticks for 1 minute and then leave. During this time, the time until the start of solidification and the time required for solidification are measured. (The size of the tempura pan is about 27cm in diameter,
According to this test method, the amount of alkali (sodium hydroxide) required to solidify a predetermined amount of tempura oil is determined, and the difference between the dispersant according to the present invention and the conventional dispersant is evaluated. I do.

【0031】[0031]

【実施例1〜4及び比較例1】次に具体的な実施例につ
いて説明する。実施例1〜4及び比較例1(成分組成は
表1に示す通り。単位は (g))は評価試験法1を適用
し、油処理剤を用いたときに、50ml (45g)のてんぷら
油の廃油を固化するに要した油処理剤の量、及び正味ア
ルカリ(水酸化ナトリウム)量を求めた。なお、5分以
内に20rpm以下に達した場合を固化(○印)と評価し、
表2に記載した。
Examples 1 to 4 and Comparative Example 1 Next, specific examples will be described. In Examples 1 to 4 and Comparative Example 1 (the composition of the components is as shown in Table 1. The unit is (g)), the evaluation test method 1 was applied. When the dispersant was used, 50 ml (45 g) of tempura oil was used. The amount of dispersant required to solidify the waste oil and the amount of net alkali (sodium hydroxide) were determined. In addition, when it reaches 20 rpm or less within 5 minutes, it is evaluated as solidification (○ mark),
It is described in Table 2.

【0032】[0032]

【表1】 [Table 1]

【表2】 上記表1及び2の通り、実施例1〜4の油処理剤では50
mlの廃油を固化するのに要する水酸化ナトリウムの量は
0.36〜0.40gであった。これに対し比較例1では2.5g
以上となった。このように、従来技術の油処理剤よりも
数分の1の水酸化ナトリウムの使用量ですむことが確認
された。
[Table 2] As shown in Tables 1 and 2 above, the oil dispersants of Examples 1 to 4 had 50
The amount of sodium hydroxide required to solidify ml of waste oil is
0.36 to 0.40 g. On the other hand, in Comparative Example 1, 2.5 g
That's all. As described above, it was confirmed that the amount of sodium hydroxide used was a few times smaller than that of the conventional dispersant.

【0033】[0033]

【実施例5〜7】水酸化ナトリウムを水とエタノールの
混合液に溶解し、分散相に供する溶液を得て、連続相へ
添加し、廃油へ投入する直前に強く撹拌してW/Oエマル
ションを得てこれを用いた。
Examples 5 to 7 A W / O emulsion was prepared by dissolving sodium hydroxide in a mixture of water and ethanol to obtain a solution to be used as a dispersed phase, adding the solution to the continuous phase, and immediately stirring it immediately before charging the waste oil. This was used.

【0034】[0034]

【実施例8〜13】水酸化ナトリウムを水とエタノール
の混合溶液に溶解し分散相に供する溶液を得て、連続相
へ分散剤である界面活性剤を用いて分散させてW/Oエマ
ルションである油処理剤を得た。
Examples 8 to 13 Sodium hydroxide was dissolved in a mixed solution of water and ethanol to obtain a solution to be used as a dispersed phase, and dispersed in a continuous phase using a surfactant as a dispersant. A dispersant was obtained.

【0035】実施例5〜13(成分組成は表3に示す通
り。単位は(g) )および後述の比較例2〜6(成分組成
は表4に示す通り。単位は(g) )は、評価試験法2を適
用し、本発明の油処理剤の効果である廃油の固化性能
を、混合の容易性・固化状態・固化速度を観察し、次の
評価基準により従来技術との違いを明らかにする。な
お、実施例5〜13及び比較例2〜6の評価を表5にま
とめた。
Examples 5 to 13 (component compositions are as shown in Table 3; units are (g)) and Comparative Examples 2 to 6 described later (component compositions are as shown in Table 4 and units are (g)) are as follows: Applying Evaluation Test Method 2, observing the solidification performance of waste oil, which is the effect of the dispersant of the present invention, the ease of mixing, the solidification state, and the solidification rate, and clarifying the difference from the conventional technology by the following evaluation criteria To Table 5 summarizes the evaluations of Examples 5 to 13 and Comparative Examples 2 to 6.

【0036】[廃油との混合の容易性] ◎;特に混合しやすい ○;混合しやすい △;やや混合しにくい ×;混合しにくい [固化状態] ◎;全体的に均一に固化 ○;ほぼ全体的に固化。一部柔らかい部分有り。[Ease of mixing with waste oil] ◎: Particularly easy to mix ○: Easy to mix △; Slightly hard to mix ×: Hard to mix [solidified state] ;: Solidified uniformly uniformly ○: Almost the whole Solidified. Some soft parts.

【0037】△;部分的に固化。一部固化しきれない廃
油分有り。
Δ: Partially solidified. There is waste oil that cannot be partially solidified.

【0038】×;固化しない。X; does not solidify.

【0039】[固化速度] ◎;適度な速度で固化。[Solidification rate] A: Solidification at an appropriate rate.

【0040】○;ゆっくりと固化。○: solidified slowly.

【0041】△;固化速度が速過ぎ部分的に固化。(4): The solidification rate is too high and the solidification is partially achieved.

【0042】×;固化しない。X; does not solidify.

【0043】なお、固化速度が速過ぎるとは、油処理剤
が廃油全体に行き渡る前に部分的に固化が始まり、最終
的には固化部分と固化しきれない油部分が存在するた
め、廃油全体を処理することができない事を意味する。
When the solidification rate is too fast, solidification begins partially before the dispersant spreads over the entire waste oil, and finally there is a solidified part and an oil part that cannot be solidified, so that the entire waste oil is solidified. Cannot be processed.

【0044】[0044]

【表3】 本発明の実施例5〜13までの油処理剤と比較するた
め、従来技術の油処理剤について下記のとおり試験し
た。
[Table 3] Prior art dispersants were tested as follows for comparison with the dispersants of Examples 5-13 of the present invention.

【0045】[0045]

【比較例2〜3】水酸化ナトリウムを水に溶解したもの
に、プロピレングリコール、エタノール、ジエチレング
リコールモノイソブチルエーテル、ラウリルアミンオキ
シド水溶液の混合溶液を加え、均一な液状の油処理剤を
得た。
Comparative Examples 2-3 A mixed solution of propylene glycol, ethanol, diethylene glycol monoisobutyl ether and an aqueous solution of laurylamine oxide was added to a solution of sodium hydroxide in water to obtain a uniform liquid dispersant.

【0046】なお、比較例2及び3の重量は、表4の通
りである。
The weights of Comparative Examples 2 and 3 are as shown in Table 4.

【0047】[0047]

【比較例4〜5】水酸化ナトリウムを水に溶解したもの
に、2-フェノキシエタノール、ポリプロピレングリコー
ル、イソプロピルアルコール、ラウリルアミンオキシド
水溶液を混合した溶液を加え、均一な液状の油処理剤を
得た。
Comparative Examples 4 and 5 A solution obtained by mixing 2-phenoxyethanol, polypropylene glycol, isopropyl alcohol and an aqueous solution of laurylamine oxide in a solution of sodium hydroxide in water was added to obtain a uniform liquid dispersant.

【0048】なお、比較例4〜5の重量は、表4の通り
である。
The weights of Comparative Examples 4 and 5 are as shown in Table 4.

【0049】[0049]

【比較例6】表4に示すとおり12-ヒドロキシステサリ
ン酸15gを比較例6の油処理剤とした。なお、性状は粉
末であった。
Comparative Example 6 As shown in Table 4, 15 g of 12-hydroxystearic acid was used as the dispersant of Comparative Example 6. The properties were powder.

【0050】[0050]

【表4】 [Table 4]

【表5】 上記の通り、実施例5〜13は、比較例2〜6の油処理
剤に比べ、混合が容易で、適度な速度で固化が進行し、
廃油を全体的に均一に固化することができた。
[Table 5] As described above, Examples 5 to 13 are easier to mix than the dispersants of Comparative Examples 2 to 6, and solidification proceeds at an appropriate speed.
The waste oil could be solidified uniformly throughout.

【0051】[0051]

【実施例14及び比較例7】[評価試験方法3]固化した
廃油の固さを調べる基準として、直径2cm、重量6g
のガラス球を固化した廃油上に静置し、10分後に沈降
距離を測定した。また目視による観察、廃棄の仕方を確
認し、従来技術との違いを明らかにする。
Example 14 and Comparative Example 7 [Evaluation Test Method 3] As a standard for examining the hardness of the solidified waste oil, the diameter was 2 cm and the weight was 6 g.
Was placed on the solidified waste oil, and the settling distance was measured after 10 minutes. In addition, the method of visual observation and disposal is confirmed, and the difference from the conventional technology is clarified.

【0052】実施例14及び比較例7(成分組成は表6
に示す通り。単位は(g) )は評価試験方法3を適用し、
固化後の廃油の固さについて観察した。なお、実施例1
4及び比較例7の評価を表7にまとめた。
Example 14 and Comparative Example 7 (component compositions are shown in Table 6
As shown. The unit is (g)), apply evaluation test method 3,
The hardness of the waste oil after solidification was observed. Example 1
Table 7 summarizes the evaluations of 4 and Comparative Example 7.

【0053】[0053]

【表6】 [Table 6]

【表7】 上記の通り実施例14は、比較例7の油処理剤に比べ、
廃油を全体的に固化でき、かつ油分が残らないため廃棄
も容易に行えることが確認された。
[Table 7] As described above, Example 14 was compared with the dispersant of Comparative Example 7,
It has been confirmed that the waste oil can be solidified as a whole and the oil can be easily disposed because no oil remains.

【0054】[0054]

【実施例15〜17】[評価試験方法4]油処理剤の調合
は初めに分散相である水酸化ナトリウム、水、アルコー
ルの混合溶液を作成し、これを界面活性剤をあらかじめ
添加しておいた連続相の鉱油に滴下しながら20分間攪
拌した。攪拌の際、攪拌機の回転数を加減することによ
って、分散相の粒子の径を3段階に変化させた。粒子の
径の測定は顕微鏡観察及びその写真撮影を行い平均粒子
径を計測し確認した。この評価方法により分散相の粒子
の径と固化速度の関係について確認した。
Examples 15 to 17 [Evaluation Test Method 4] The dispersant was prepared by first preparing a mixed solution of sodium hydroxide, water and alcohol, which are dispersed phases, and adding a surfactant in advance. The mixture was stirred for 20 minutes while being dropped into the continuous phase mineral oil. During the stirring, the diameter of the dispersed phase particles was changed in three stages by adjusting the number of revolutions of the stirrer. The particle diameter was measured by microscopic observation and photographing, and the average particle diameter was measured and confirmed. By this evaluation method, the relationship between the particle size of the dispersed phase and the solidification rate was confirmed.

【0055】実施例15〜17の成分組成及び攪拌機の
回転数、粒子を表8に示す。なお、上記評価方法4を用
いて試験した結果を表9に示す。及び表9に基づき固化
状態について図1に示すグラフを用いて説明する。
Table 8 shows the component compositions, the number of revolutions of the stirrer, and the particles of Examples 15 to 17. Table 9 shows the results of a test performed using the above evaluation method 4. The solidification state will be described based on Table 9 and the graph shown in FIG.

【0056】[0056]

【表8】 [Table 8]

【表9】 上記表8、表9、図1より分散相の粒子径が小さいほど
固化速度が速いと言うことが確認された。また言い換え
ると、分散相の粒子径によって固化速度の制御も可能で
あると言うことが確認された。
[Table 9] From Tables 8 and 9, and FIG. 1, it was confirmed that the smaller the particle size of the dispersed phase, the faster the solidification rate. In other words, it was confirmed that the solidification rate could be controlled by the particle size of the dispersed phase.

【0057】[0057]

【発明の効果】以上、詳述したように本発明における油
処理剤は、廃油を常温付近で凝固させることができ、廃
油と混ざりやすく、強アルカリの使用量を減らす等の種
々の効果を有する。
As described in detail above, the dispersant of the present invention can coagulate waste oil at around normal temperature, easily mix with waste oil, and have various effects such as reducing the amount of strong alkali used. .

【図面の簡単な説明】[Brief description of the drawings]

【図1】実施例15、16、17における固化状態を示
す説明図
FIG. 1 is an explanatory view showing a solidified state in Examples 15, 16 and 17.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 笠原 達男 東京都台東区東上野2丁目21番14号 株式 会社白元内 (72)発明者 椎谷 智洋 東京都台東区東上野2丁目21番14号 株式 会社白元内 Fターム(参考) 4H059 AA03 AA04 AA09 AA12 BA01 BA02 BA12 BA16 BA17 BA26 BA42 BA49 BB02 BC03 BC13 BC33 CA94 DA16 DA24 DA30 EA11 EA13 EA15  ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Tatsuo Kasahara 2-21-14 Higashiueno, Taito-ku, Tokyo Co., Ltd. (72) Inventor Tomohiro Shiiya 2-21-14 Higashiueno, Taito-ku, Tokyo 4H059 AA03 AA04 AA09 AA12 BA01 BA02 BA12 BA16 BA17 BA26 BA42 BA49 BB02 BC03 BC13 BC33 CA94 DA16 DA24 DA30 EA11 EA13 EA15

Claims (9)

【特許請求の範囲】[Claims] 【請求項1】油性の連続相に水性の分散相が分散されて
なるW/O型エマルションの油処理剤であって、前記分散
相が水または水とアルコールを含む溶液、あるいは水を
含まないアルコール溶液に水酸化ナトリウムなどのアル
カリの水酸化物、または、ナトリウムアルコキシドなど
の金属アルコキシドを混合してなるアルカリ混合溶液で
あり、かつ前記連続相が前記分散相と相溶性のない液体
とからなるW/O型エマルションであることを特徴とする
油処理剤。
1. An oil dispersant for a W / O emulsion in which an aqueous dispersion phase is dispersed in an oily continuous phase, wherein the dispersion phase contains water, a solution containing water and an alcohol, or does not contain water. An alkali mixed solution obtained by mixing an alcohol solution with an alkali hydroxide such as sodium hydroxide or a metal alkoxide such as sodium alkoxide, and wherein the continuous phase is a liquid incompatible with the dispersed phase. Dispersant characterized by being a W / O emulsion.
【請求項2】前記分散相を前記連続相に分散させる分散
剤として、界面活性剤を用いてなるW/O型エマルション
であることを特徴とする請求項1に記載の油処理剤。
2. The dispersant according to claim 1, wherein the dispersant for dispersing the dispersed phase in the continuous phase is a W / O emulsion using a surfactant.
【請求項3】前記分散相の粒子の径を15μm以下とした
ことを特徴とする請求項1又は2に記載の油処理剤。
3. The dispersant according to claim 1, wherein the particle diameter of the dispersed phase is 15 μm or less.
【請求項4】前記界面活性剤が、ポリアルケニル琥珀酸
イミド、またはその誘導体、ポリアルケニル琥珀酸アミ
ド、またはその誘導体、ポリオレフィンアミド系または
その誘導体、アルキル/アルケニルアミン系またはその
誘導体、ポリオレフィンアミドアルケンアミン系または
その誘導体、ポリオキシエチレン系、ポリオキシフェニ
ルエーテル系、アルカリ金属およびアルカリ土類金属石
鹸系の界面活性剤を1種または2種以上用いてなること
を特徴とする請求項2に記載の油処理剤。
4. The method according to claim 1, wherein the surfactant is a polyalkenyl succinimide or a derivative thereof, a polyalkenyl succinamide or a derivative thereof, a polyolefin amide or a derivative thereof, an alkyl / alkenyl amine or a derivative thereof, a polyolefin amide alkene. 3. The composition according to claim 2, wherein one or more of an amine or a derivative thereof, a polyoxyethylene, a polyoxyphenyl ether, an alkali metal and an alkaline earth metal soap are used. Dispersant.
【請求項5】前記連続相が、鉱物油または合成油である
ことを特徴とする請求項1に記載の油処理剤。
5. The dispersant according to claim 1, wherein the continuous phase is a mineral oil or a synthetic oil.
【請求項6】前記連続相が、鉱物油である潤滑油基油の
スピンドル油、トランス油、ニュートラル油、ブライト
ストック油や、燃料油の石油ナフサ、ガソリン、灯油、
軽油や、プロセスオイルや、流動パラフィンや、合成油
である合成系エーテル油や、合成系ポリアルキレングリ
コール油、合成系ポリアルファオレフィン、アルキルベ
ンゼン油、シリコンオイルの中から選ばれる1種または
2種以上のオイル分を用いてなることを特徴とする請求
項5に記載の油処理剤。
6. The continuous phase is a mineral base oil such as a spindle oil of a lubricating base oil, a transformer oil, a neutral oil, a bright stock oil, a fuel oil such as petroleum naphtha, gasoline, kerosene,
One or more selected from light oils, process oils, liquid paraffin, synthetic ether oils that are synthetic oils, synthetic polyalkylene glycol oils, synthetic polyalphaolefins, alkylbenzene oils, and silicone oils 6. The dispersant according to claim 5, wherein the oil component is used.
【請求項7】水酸化ナトリウムを溶解してなる水とエタ
ノールの混合溶液からなる分散相と、引火点50℃以上の
パラフィン炭化水素、オレフィン系炭化水素、芳香族炭
化水素の中から選ばれる1種または2種以上の連続相
と、該分散相を界面活性剤によって略粒径10μmの粒子
として前記連続相に分散させてなるW/O型エマルション
であることを特徴とする油処理剤。
7. A dispersed phase comprising a mixed solution of water and ethanol obtained by dissolving sodium hydroxide, and a paraffin hydrocarbon, an olefinic hydrocarbon or an aromatic hydrocarbon having a flash point of 50 ° C. or higher. An oil treating agent, which is a W / O-type emulsion obtained by dispersing a kind or two or more kinds of continuous phases and the dispersed phase as particles having a particle diameter of about 10 μm with a surfactant in the continuous phase.
【請求項8】前記分散相が、水酸化ナトリウム2〜30%、
水1〜40%、エタノール2〜80%を含んでなり、かつ、前記
連続相が鉱物油であることを特徴とする請求項1に記載
の油処理剤。
8. The method according to claim 1, wherein the dispersed phase comprises 2 to 30% of sodium hydroxide,
The dispersant according to claim 1, comprising 1 to 40% of water and 2 to 80% of ethanol, and wherein the continuous phase is a mineral oil.
【請求項9】前記油処理剤に水酸化カルシウム、硫酸カ
ルシウム、ソーダライム、ペントナイト、カオリナイ
ト、等の粉末を添加したことを特徴とする請求項1乃至
8のいずれか一つに記載の油処理剤。
9. The method according to claim 1, wherein a powder of calcium hydroxide, calcium sulfate, soda lime, pentonite, kaolinite, or the like is added to the dispersant. Dispersant.
JP5539998A 1998-03-06 1998-03-06 Dispersant Expired - Fee Related JP3564292B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP5539998A JP3564292B2 (en) 1998-03-06 1998-03-06 Dispersant
PCT/JP1999/001015 WO1999045086A1 (en) 1998-03-06 1999-03-03 Treating agent for oil
AU27452/99A AU2745299A (en) 1998-03-06 1999-03-03 Treating agent for oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5539998A JP3564292B2 (en) 1998-03-06 1998-03-06 Dispersant

Publications (2)

Publication Number Publication Date
JP2001089753A true JP2001089753A (en) 2001-04-03
JP3564292B2 JP3564292B2 (en) 2004-09-08

Family

ID=12997467

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5539998A Expired - Fee Related JP3564292B2 (en) 1998-03-06 1998-03-06 Dispersant

Country Status (3)

Country Link
JP (1) JP3564292B2 (en)
AU (1) AU2745299A (en)
WO (1) WO1999045086A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007284628A (en) * 2006-04-20 2007-11-01 Arakawa Chem Ind Co Ltd Metal soap, method for producing the same and oil-absorbing material

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61116000A (en) * 1984-11-09 1986-06-03 和協化学工業株式会社 Saponification agent of waste edible oil
JPH05263100A (en) * 1992-03-17 1993-10-12 Asuka Kk Saponifying agent for used edible oil and saponification of used edible oil therewith
JPH0913072A (en) * 1995-06-30 1997-01-14 Sairaido Koryo Kk Treating agent capable of partly saponifying and solidifying oil saponifiable and liquid at ordinary temperature like triglyceride and its production

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007284628A (en) * 2006-04-20 2007-11-01 Arakawa Chem Ind Co Ltd Metal soap, method for producing the same and oil-absorbing material

Also Published As

Publication number Publication date
AU2745299A (en) 1999-09-20
WO1999045086A1 (en) 1999-09-10
JP3564292B2 (en) 2004-09-08

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