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WO1999045086A1 - Treating agent for oil - Google Patents

Treating agent for oil Download PDF

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Publication number
WO1999045086A1
WO1999045086A1 PCT/JP1999/001015 JP9901015W WO9945086A1 WO 1999045086 A1 WO1999045086 A1 WO 1999045086A1 JP 9901015 W JP9901015 W JP 9901015W WO 9945086 A1 WO9945086 A1 WO 9945086A1
Authority
WO
WIPO (PCT)
Prior art keywords
oil
dispersant
dispersed phase
phase
continuous 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.)
Ceased
Application number
PCT/JP1999/001015
Other languages
French (fr)
Japanese (ja)
Inventor
Tatsuo Kasahara
Tomohiro Shiiya
Kunimitsu Tamura
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.)
Hakugen Co Ltd
Prest Corp
Original Assignee
Hakugen Co Ltd
Prest Corp
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 Hakugen Co Ltd, Prest Corp filed Critical Hakugen Co Ltd
Priority to US09/623,408 priority Critical patent/US6653355B1/en
Priority to AU27452/99A priority patent/AU2745299A/en
Publication of WO1999045086A1 publication Critical patent/WO1999045086A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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

Definitions

  • the present invention relates to an oil treatment agent, and more particularly to an oil treatment agent for coagulating oil used for treating tempura oil for home use and edible waste oil for business use. Background technology
  • waste oil used tempura oil and commercial edible waste oil (hereinafter referred to as “waste oil”), low-molecular-weight polyethylene / paraffin, etc., was injected into the waste oil, coagulated and discarded.
  • waste oil used tempura oil and commercial edible waste oil
  • an appropriate amount of 12-hydroxyxearateric acid is added to waste edible oil, heated and dissolved without allowing water to coexist, and then cooled.
  • a solidification method is proposed.
  • waste oil can be coagulated between room temperature and about 90 ° C.
  • this experimental accelerator and waste oil can be used.
  • the contact area with the oil was small, and the compatibility with the waste oil was low.
  • such an accelerator is difficult to mix and the reaction is difficult to proceed, so that an excessive strong alkali must be used, and the corrosive strong alkali comes into contact with the human body during use. This can damage the skin and is not very desirable.
  • the corrosiveness of the strong alkali is also unfavorable because it may corrode metals, and may corrode cooking utensils such as tempura pans.
  • the present invention has been made in view of the above-mentioned conventional drawbacks, and provides an oil dispersant that can solidify waste oil even at around normal temperature, is easily mixed with waste oil, and can reduce the amount of strong alkali used. It is an object. Disclosure of the invention
  • a first dispersant of the present invention is a W / 0-type emulsion dispersant obtained by dispersing an aqueous dispersion phase in an oily continuous phase,
  • the phase is water or a solution containing water and alcohol, or a water-free alcohol solution in an alkali hydroxide such as sodium hydroxide, or sodium alcohol.
  • An alkali mixed solution obtained by mixing a metal alkoxide such as an oxide, and the continuous phase is a W / 0 emulsion comprising the dispersed phase and a liquid having no compatibility.
  • the second oil dispersant of the present invention is the W / 0 emulsion according to the first oil dispersant, wherein a surfactant is used as a dispersant for dispersing the dispersed phase in the continuous phase.
  • a third dispersant according to the present invention is characterized in that, in the second dispersant, the particle size of the dispersed phase is 15 / zm or less.
  • the fourth dispersant according to the present invention is the second dispersant, wherein the surfactant is a polyalkenyl succinic acid amide or a derivative thereof, a polyalkenyl succinic acid amide or a derivative thereof.
  • the surfactant is a polyalkenyl succinic acid amide or a derivative thereof, a polyalkenyl succinic acid amide or a derivative thereof.
  • Polyolefinamides or derivatives thereof, alkylnoalkenylamines or derivatives thereof, polyolefinamidealkamines or derivatives thereof, polyoxyethylenes, polyoxyphenylethers, alkali metals and alkaline earth metals It is characterized by using one or more genus stone surfactants.
  • a fifth dispersant of the present invention is characterized in that, in the first dispersant, the particle size of the dispersed phase is 15 / zm or less.
  • a sixth dispersant according to the present invention is the first dispersant, wherein the continuous phase is a mineral oil or a synthetic oil.
  • a seventh dispersant according to the present invention is the dispersant according to the sixth aspect, wherein the continuous phase is a spindle oil of a lubricating base oil, which is a mineral oil, a translucent oil, a neutral oil, or a brittle oil.
  • a lubricating base oil which is a mineral oil, a translucent oil, a neutral oil, or a brittle oil.
  • the eighth dispersant of the present invention is a dispersant comprising a mixed solution of water and ethanol in which sodium hydroxide is dissolved, and a paraffin hydrocarbon having a flash point of 50 ° C or higher.
  • a ninth dispersant of the present invention is the dispersant according to the first aspect, wherein the dispersed phase comprises 2 to 30% of sodium hydroxide, 1 to 40% of water, and 2 to 80% of ethanol. And the continuous phase is a mineral oil.
  • the dispersant of the present invention is a W / 0 type emulsion having a dispersed phase of an alkali hydroxide or an alkali mixed solution
  • minute and innumerable particles of alkali are added.
  • minute and innumerable alkalis can be uniformly dispersed in the waste oil.
  • a small amount of the alkali can sufficiently secure the contact area between the waste oil and the alkali solution.
  • the waste oil can be solidified and processed quickly.
  • FIG. 1 is an explanatory diagram showing a solidified state in Examples 15 to 16 of the present invention. Best form to carry out the invention
  • the dispersant is used as a W / 0 emulsion dispersant
  • the dispersed phase in the emulsion is a particle having a particle size of 15 zm or less, and a high concentration of hydroxide in the particle.
  • edible oils and the like are basically fatty acid esters of fatty acids and glycerin in chemical structure.
  • an alkali such as sodium hydroxide
  • the fatty acid soda that is, stone test
  • Producing lithology usually requires the caustic required to completely convert the ester.
  • the present invention is based on the premise that waste oil is basically solidified by adding caustic alkali to edible oil and utilizing the solidification phenomenon of stone aya refining. In such waste oil treatment, it is not necessary to test all waste oils, and partial testing is sufficient. In other words, it is sufficient if solidification is achieved by partial tanning (the point different from producing ishiken is solidification, and it is not necessary to fully test 100%).
  • a solution-type solidifying agent for example, a homogeneous solution in which sodium hydroxide is dissolved in a base material such as water-alcohol has been studied.
  • the authors confirmed that a high-concentration alkaline solution was required to solidify waste oil to a practical hardness with a certain amount of solidification agent in the solution-type solidification agent.
  • a high-concentration alkaline solution was required to solidify waste oil to a practical hardness with a certain amount of solidification agent in the solution-type solidification agent.
  • an excessive amount of a high-concentration alkaline solution is required.
  • Further disadvantages of this solution-type high-concentration alkaline solution solidifying agent include safety problems at the time of skin contact due to high alkali concentration and corrosiveness to cooking utensils such as tempura pans. .
  • the present inventors have conducted intensive studies on these causes, and as a result, the conventional solution-type solidifying agent is a uniform liquid as a whole, and when this is mixed with edible oil in a container such as a tempura pan,
  • the artificial mixing with chopsticks and spatula etc. by housewives or workers etc. does not sufficiently mix the treatment agent and edible oil, and the contact area between the alkaline solution and the tempura oil is small. Reaction rate is low I inferred.
  • it has been necessary to add an excessive amount of alkali or to make the concentration too high for example, a high concentration of 20 to 40% based on the entire treatment agent).
  • the contact between the alkaline solution and the waste oil such as edible oil is performed only by stirring after the dispersant is added, and the waste oil is not used.
  • the particle size of the particulate component increases, which reduces the contact area between the alkaline solution and the waste oil.
  • the present invention uses a W / 0 emulsion as the dispersant and disperses the alkaline solution with fine particles from the beginning, so that the waste oil and the alkaline solution can be slightly stirred. This ensures a large contact area with the device.
  • the dispersant according to the present invention is obtained by mixing and stirring a solution of an alcohol in water and alcohol with a solution having no or low compatibility with the solution.
  • the gist is to provide a dispersant that is a water-in-oil type (W / 0 type) emulsion.
  • the dispersed phase A mixed solution of the two is used.
  • the continuous phase must be a liquid base material that does not dissolve in the dispersed phase components (that is, is incompatible or small).
  • oil such as mineral oil or synthetic oil is used for the continuous phase.
  • a mineral oil or a synthetic oil is preferably used, and one or a mixture of two or more may be used.
  • a mineral oil a highly refined white oil is used. Is also good.
  • mineral oils such as lubricating base oils such as spindle oil, transformer oil, neutral oil, bright stock oil, and fuel oils such as petroleum naphtha, gasoline, kerosene, light oil, process oil, and synthetic oil Synthetic oils such as synthetic ester oils, synthetic ether oils, synthetic polyalkylene glycol oils, synthetic polyalphaolefins, alkylbenzene oils, and silicon oils.
  • the ratio of the continuous phase to the whole W / 0 emulsion is not particularly limited, but it is preferable to use a continuous phase of about 40 to 95%.
  • the alkali used for the dispersed phase is not particularly limited as long as it is a strong alkali, but sodium hydroxide, potassium hydroxide, lithium hydroxide, barium hydroxide and the like are used. Preferably, sodium hydroxide is used.
  • sodium alkoxide is preferable, and sodium ethoxide, sodium methoxide or a mixture thereof is used.
  • the alkali concentration of the alkaline solution of the dispersed phase a concentration of about 3 to 60% is preferable, and a concentration of about 30% is more preferably used.
  • the particle size of the alkaline mixed solution as the disperse phase is not particularly limited, and a particle size of 15 / ⁇ or less is used, preferably 10 / m or less, and more preferably 3 / m 2 or less. / m or less is good. If the particle size is large, the reactivity is reduced, and the dispersion stability as an emulsion is deteriorated.
  • powder is used as a component of the dispersant for increasing the amount or diluting the alkali concentration.
  • powder for example, calcium hydroxide, calcium sulfate, bentonites, olizonites, etc.
  • Carbonaceous particles such as perlite or carbon black or activated carbon may be mixed.
  • a surfactant in order to form a W / 0 emulsion, can be preferably used as a dispersant for dispersing an alkaline mixed solution in an oil component.
  • the dispersant may be vigorously stirred at the time of use (immediately before the dispersant of the present invention is added to the waste oil) and then added to the waste oil.
  • the dispersant is of a type that is filled into a bottle for each use, shaking the entire bottle saves time for stirring. It is preferable as it is not inconvenient.
  • the surfactant is not particularly limited as long as the dispersed phase can be stably dispersed in the continuous phase for a long time, but the properties of the continuous phase oil, the concentration of the dispersed phase, and the like are not limited.
  • the type and amount of use may be appropriately adjusted in consideration of such factors.
  • One or two surfactants based on alkenylamines or their derivatives, polyolefinamide alkenamines or derivatives thereof, polyoxyethylene, polyoxyphenyl ether, alkali metal and alkaline earth metal stones The above can be used.
  • the dispersant of the present invention is added to waste oil at around room temperature and stirred. Then, the waste oil and the dispersant immediately start reacting and solidify in about 1 minute, so they can be separated from the pot and discarded.
  • the dispersant of the present invention is a W / 0 type emulsion having a dispersed phase of an alkali hydroxide or an alkali mixed solution.
  • the particles are dispersed in the waste oil and initiate the experimental reaction.
  • the dispersant can uniformly disperse minute and innumerable alcohols in the waste oil, and since the above-mentioned alkali is a droplet, a small amount of an alkaline solution can be used to dispose the waste oil and the alkali.
  • the contact area of the solution can be sufficiently secured, and the waste oil can be quickly solidified and treated.
  • Magnetic Stirrer I Use a commercially available glass beaker and a magnetic stirrer (Magnetic Stirrer I).
  • the magnetic stirrer used was one whose rotation speed of the stirrer could be read directly by LED display.
  • the degree of reduction in the rotational speed differs depending on the degree of solidification, and the more solidified, the lower the rotational speed. In other words, the degree of solidification can be confirmed by observing the situation of the decrease in the rotational speed.
  • test dispersant is added to the beaker, and the number of revolutions of the stirrer is immediately read to observe and record the change over time.
  • the dispersant having excellent solidification performance rapidly solidifies because the solidification occurs in a short time.
  • the solidification criteria were 20 rpm (20 revolutions per minute), and the required amount of alkali (sodium hydroxide) in terms of solidification required and the solidification time were determined. [Evaluation test method 2]
  • tempura pan at room temperature, add 600 ml of waste oil (room temperature) of tempura oil. Immediately after adding 100ml of dispersant, mix well with chopsticks for 1 minute and then leave. During this time, measure the time until solidification starts and the time required for solidification. (The size of the tempura pot is about 27 cm in diameter ⁇ i »and about 5 cm in depth.)
  • the amount of alkali (sodium hydroxide) required to solidify a predetermined amount of tempura oil was determined, and the difference between the dispersant according to the present invention and the dispersant according to the prior art was evaluated. I do.
  • Example 1 the composition of the components is as shown in Table 1.
  • the unit is (g)
  • the evaluation test method 1 was applied.
  • 50 ml 45 g
  • the amount of dispersant required to solidify the waste oil of the balance oil and the net amount of sodium hydroxide (sodium hydroxide) were determined.
  • it reached 20 rpm or less within 5 minutes it was evaluated as solidification (marked with ⁇ ) and described in Table 2.
  • Sodium hydroxide is dissolved in a mixed solution of water and ethanol to obtain a solution to be used for the dispersed phase, added to the continuous phase, and stirred vigorously immediately before pouring into waste oil to obtain a W / 0 emulsion. This was used.
  • Examples 5 to 13 Ingredient composition is as shown in Table 3. The unit is (g)). Comparative Examples 2 to 6 described below (Ingredient composition is as shown in Table 4. The unit is (g)).
  • Evaluation Test Method 2 the solidification performance of the waste oil, which is the effect of the dispersant of the present invention, was evaluated for the ease of mixing, the solidification state, and the solidification rate. Observe and clarify the difference from the conventional technology by the following evaluation criteria. Table 5 summarizes the evaluations of Examples 5 to 13 and Comparative Examples 2 to 6.
  • A solidified at an appropriate speed.
  • Examples 5 to 13 are easier to mix than the dispersants of Comparative Examples 2 to 6, solidification proceeds at an appropriate speed, and the waste oil can be uniformly solidified as a whole. Was.
  • Example 14 and Comparative Example 7 the composition of the components is as shown in Table 6. The unit is (g)), the evaluation test method 3 was applied, and the hardness of the waste oil after solidification was observed.
  • Table 7 summarizes the evaluations of Example 14 and Comparative Example 7. (Table 6)
  • Example 14 compared with the dispersant of Comparative Example 7, the waste oil could be solidified as a whole, and the oil could be easily disposed of because no oil remains.
  • the dispersant is prepared by first preparing a mixed solution of sodium hydroxide and alcohol, which are the dispersed phases, and dropping it into the continuous phase mineral oil to which the surfactant has been added in advance. Stirred for 20 minutes. At the time of stirring, the diameter of the dispersed phase particles was changed in three stages by adjusting the rotation speed of the stirrer. The particle diameter was measured by microscopic observation and photographing, and the average particle diameter was measured and confirmed. With this evaluation method, the relationship between the particle size of the dispersed phase and the solidification rate was confirmed.
  • Table 8 shows the component compositions, the rotation speeds of the stirrers, and the particles of Examples 15 to 17.
  • Table 9 shows the results of tests using the above evaluation method 4. The solidification state will be described with reference to Table 9 and the graph shown in Fig. 1.
  • Dispersed phase water 8.0g
  • the oil dispersant according to the present invention can solidify waste oil at around normal temperature, and is easily mixed with waste oil. It has various effects such as reducing the use of strong alkaline.

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  • 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

A treating agent for oils which is a W/O emulsion comprising an oily continuous phase and an aqueous phase dispersed therein, wherein the dispersed phase is an alkali solution obtained by mixing water, a solution comprising water and an alcohol, or a water-free alcohol solution with an alkali hydroxide such as sodium hydroxide or with a metal alkoxide such as a sodium alkoxide and the continuous phase comprises a liquid incompatible with the dispersed phase.

Description

明 細 書 油 処理剤 技 術 分 野  Description Oil dispersant technology

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。 背 景 技術  The present invention relates to an oil treatment agent, and more particularly to an oil treatment agent for coagulating oil used for treating tempura oil for home use and edible waste oil for business use. Background technology

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ゃパラフ イン等を廃油に投入し、 凝固させ廃棄していた。 また、 特公昭 6 0 - 054092号公報に記載の発明では、 1 2-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- 01 3072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験化する 場合完全験化に要するアルカリの量の 1 /6〜1 /3で鐄化し、 その 験化開始後約 1 〜 3分で固化するための溶液型 (均一系) の験 化促進剤を提案している。  Conventionally, in order to treat used tempura oil and commercial edible waste oil (hereinafter referred to as “waste oil”), low-molecular-weight polyethylene / paraffin, etc., was injected into the waste oil, coagulated and discarded. In addition, in the invention described in Japanese Patent Publication No. 60-054092, an appropriate amount of 12-hydroxyxearateric acid is added to waste edible oil, heated and dissolved without allowing water to coexist, and then cooled. A solidification method is proposed. In the invention described in Japanese Patent Application Laid-Open No. 9-013072, when an oil or fat that is liquid at normal temperature is tested with an alkali such as sodium hydroxide and potassium hydroxide, the alkali required for complete testing We have proposed a solution-type (homogeneous) test accelerator for solidification in 1/6 to 1/3 of the volume and solidification in about 1 to 3 minutes after the start of the test.

しかしながら、 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。  However, when low-molecular polyethylene or paraffin is used, there is a problem that the waste oil does not solidify unless added at a high temperature.

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。 In the invention described in Japanese Patent Publication No. 60-054092, waste oil If the oil was not added in a short time, it would not coagulate, and it had to be heated to treat the cooled oil. In addition, there is another problem that the waste oil solidifies only after the temperature of the waste oil drops to around room temperature, which takes time and labor.

また、 特開平 9- 01 3072号公報に記載の発明では、 常温から 9 0 °C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 液であるのでこの験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、 このよ うな験化促進剤は混ざりにく く 験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、 皮膚を損傷する虞があり、 あまり好ま しく ない。 また、 強アルカ リ の腐食性は、 金属も侵す虞があるため、 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 the solution is a homogeneous solution, this experimental accelerator and waste oil can be used. The contact area with the oil was small, and the compatibility with the waste oil was low. Furthermore, such an accelerator is difficult to mix and the reaction is difficult to proceed, so that an excessive strong alkali must be used, and the corrosive strong alkali comes into contact with the human body during use. This can damage the skin and is not very desirable. In addition, the corrosiveness of the strong alkali is also unfavorable because it may corrode metals, and may corrode cooking utensils such as tempura pans.

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。 発 明 の 開 示  The present invention has been made in view of the above-mentioned conventional drawbacks, and provides an oil dispersant that can solidify waste oil even at around normal temperature, is easily mixed with waste oil, and can reduce the amount of strong alkali used. It is an object. Disclosure of the invention

上記目的を達成するために、 本発明の第 1の油処理剤は、 油 性の連続相に水性の分散相が分散されてなる W/0型エマルシヨ 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/0型エマルシヨ ンであることを特徴とする。 In order to achieve the above object, a first dispersant of the present invention is a W / 0-type emulsion dispersant obtained by dispersing an aqueous dispersion phase in an oily continuous phase, The phase is water or a solution containing water and alcohol, or a water-free alcohol solution in an alkali hydroxide such as sodium hydroxide, or sodium alcohol. An alkali mixed solution obtained by mixing a metal alkoxide such as an oxide, and the continuous phase is a W / 0 emulsion comprising the dispersed phase and a liquid having no compatibility.

本発明の第 2の油処理剤は、 上記第 1の油処理剤において、 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/0型エマルショ ンであることを特徴とする。  The second oil dispersant of the present invention is the W / 0 emulsion according to the first oil dispersant, wherein a surfactant is used as a dispersant for dispersing the dispersed phase in the continuous phase. There is a feature.

本発明の第 3の油処理剤は、 上記第 2の油処理剤において、 前記分散相の粒子の径を 1 5 /z m以下と したことを特徴とする。 本発明による第 4 の油処理剤は、 上記第 2 の油処理剤におい て、 前記界面活性剤が、 ポリアルケ-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、 ポリオレフイ ンアミ ド系またはその誘導体、 アルキルノアルケ ニルァミン系またはその誘導体、 ポリオレフインアミ ドアルケ ンァミ ン系またはその誘導体、 ポリオキシエチレン系、 ポリオ キシフエ二ルェ一テル系、 アルカリ金属おょぴアルカリ土類金 属石験系の界面活性剤を 1種または 2種以上用いてなることを 特徴とする。  A third dispersant according to the present invention is characterized in that, in the second dispersant, the particle size of the dispersed phase is 15 / zm or less. The fourth dispersant according to the present invention is the second dispersant, wherein the surfactant is a polyalkenyl succinic acid amide or a derivative thereof, a polyalkenyl succinic acid amide or a derivative thereof. Polyolefinamides or derivatives thereof, alkylnoalkenylamines or derivatives thereof, polyolefinamidealkamines or derivatives thereof, polyoxyethylenes, polyoxyphenylethers, alkali metals and alkaline earth metals It is characterized by using one or more genus stone surfactants.

本発明の第 5の油処理剤は、 上記第 1の油処理剤において、 前記分散相の粒子の径を 1 5 /z m以下と したことを特徴とする。 本発明による第 6 の油処理剤は、 上記第 1 の油処理剤におい て、 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。  A fifth dispersant of the present invention is characterized in that, in the first dispersant, the particle size of the dispersed phase is 15 / zm or less. A sixth dispersant according to the present invention is the first dispersant, wherein the continuous phase is a mineral oil or a synthetic oil.

本発明による第 7 の油処理剤は、 上記第 6 の油処理剤におい て、 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 レンダリ コール油、 合成系ポ リ アルファオレフイ 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。 A seventh dispersant according to the present invention is the dispersant according to the sixth aspect, wherein the continuous phase is a spindle oil of a lubricating base oil, which is a mineral oil, a translucent oil, a neutral oil, or a brittle oil. Stock oil or fuel oil Petroleum naphtha, gasoline, kerosene, gas oil, process oil, liquid paraffin, synthetic ether oil as synthetic oil, synthetic polyalkylene glycol oil, synthetic polyalphaolefin Or one or more oils selected from alkyl benzene oil and silicon oil.

本発明の第 8の油処理剤は、 水酸化ナ ト リ ゥムを溶解してな 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°C以 上のパラフィ ン炭化水素、 ォレフィ 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つて略粒径 1 0 ; mの粒子と して前記連続相 に分散させてなる W/0型エマルショ ンであることを特徴とする。 本発明の第 9の油処理剤は、 上記第 1の油処理剤において、 前記分散相が、 水酸化ナ ト リ ウム 2〜30%、 水 1〜40%、 ェタノ一 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。  The eighth dispersant of the present invention is a dispersant comprising a mixed solution of water and ethanol in which sodium hydroxide is dissolved, and a paraffin hydrocarbon having a flash point of 50 ° C or higher. , One or more continuous phases selected from an olefin-based hydrocarbon and an aromatic hydrocarbon, and the dispersed phase is formed into particles having a particle size of approximately 10 m by using a surfactant. It is a W / 0 type emulsion that is dispersed in a continuous phase. A ninth dispersant of the present invention is the dispersant according to the first aspect, wherein the dispersed phase comprises 2 to 30% of sodium hydroxide, 1 to 40% of water, and 2 to 80% of ethanol. And the continuous phase is a mineral oil.

本発明の油処理剤は、 アルカリの水酸化物またはアルカ リ混 合溶液の分散相を有する W/0型エマルシヨ ンと したので、 廃油に 添加された際に、 微少で無数のアルカ リ の粒子が廃油中に分散 し、 鏡化の反応が始まる。 この場合、 微少で無数のアルカリを 廃油中に均一に分散させることができ、 しかも、 上記アルカ リ は液滴であるので、 少量のアルカリで、 廃油とアルカリ溶液の 接触面積を充分に確保することが出来、 速やかに廃油を固化し て処理できる。 図 面 の 簡 単 な 説 明 第 1 図 は 、 実施 例 1 5 、 1 6 、 1 7 に お け る 固 化 状 態 を 示 す 説 明 図 で あ る 。 発 明 を 実 施 す る た め の 最 良 の 形 態 Since the dispersant of the present invention is a W / 0 type emulsion having a dispersed phase of an alkali hydroxide or an alkali mixed solution, when added to waste oil, minute and innumerable particles of alkali are added. Are dispersed in the waste oil and the mirroring reaction starts. In this case, minute and innumerable alkalis can be uniformly dispersed in the waste oil.Moreover, since the above-mentioned alkalis are droplets, a small amount of the alkali can sufficiently secure the contact area between the waste oil and the alkali solution. The waste oil can be solidified and processed quickly. Brief explanation of drawings FIG. 1 is an explanatory diagram showing a solidified state in Examples 15 to 16 of the present invention. Best form to carry out the invention

以下、 本発明の実施の形態を説明する。 本発明者らは、 鋭意 研究の結果、 次の事項に着目 し課題を解決できることを見いだ した。  Hereinafter, embodiments of the present invention will be described. As a result of earnest research, the present inventors have found that they can solve the problem by focusing on the following items.

すなわち、 油処理剤を W/0型エマルシヨ ンの油処理剤と し、 ェ マルシヨ ン中の分散相を粒子径が 1 5 z mかそれ以下の粒子であつ て粒子中に高濃度の水酸化ナ ト リ ゥム等のアルカリ溶液を閉じ こめたもので構成し、 他方、 連続相にヱマルシヨ 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、 験化反応が全体と 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。  In other words, the dispersant is used as a W / 0 emulsion dispersant, and the dispersed phase in the emulsion is a particle having a particle size of 15 zm or less, and a high concentration of hydroxide in the particle. By using a liquid that does not mix with particles in emulsion as the continuous phase, it is possible to convert a high-concentration alkaline solution into an infinite number of fine particles. The contact area between the waste oil and the alkali solution, which has become innumerable fine particles when agitated in addition to the waste oil, becomes very large, so that the experimental reaction proceeds rapidly as a whole and solidifies in a short time. I found something that could be done. At this time, the emulsion particles can be stably dispersed in the liquid as small particles by swelling micelles formed by the adsorption of a surfactant at the interface with the continuous phase.

こ こで、 本発明に至るまでの経過について説明すると、 食用 油等は化学構造的には基本的に脂肪酸とグリ セリ ンの脂肪酸ェ 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婊化反応により脂肪酸ソーダ すなわち石験が精製し固化する。 石験を製造する場合は通常、 エステルを完全に鏔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 つて石綾精製による固化現象を利用して廃油を固化することを 前提とする。 なお、 このよ うな廃油処理に際しては、 すべての 廃油を験化する必要はなく部分験化で足り る。 すなわち部分綾 化で固化が達成されれば十分である (石験を製造すること と異 なる点は固化が目的であって、 1 00%完全に験化する必要はな い) 。 Here, the course leading up to the present invention will be described. 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, the fatty acid soda, that is, stone test, is purified and solidified by the oxidation reaction. Producing lithology usually requires the caustic required to completely convert the ester. The present invention is based on the premise that waste oil is basically solidified by adding caustic alkali to edible oil and utilizing the solidification phenomenon of stone aya refining. In such waste oil treatment, it is not necessary to test all waste oils, and partial testing is sufficient. In other words, it is sufficient if solidification is achieved by partial tanning (the point different from producing ishiken is solidification, and it is not necessary to fully test 100%).

このよ うな前提に基づき、 従来から溶液型すなわち例えば水 酸化ナ ト リ ゥムを水一アルコ一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。  On the basis of such a premise, a solution-type solidifying agent, for example, a homogeneous solution in which sodium hydroxide is dissolved in a base material such as water-alcohol has been studied. The authors confirmed that a high-concentration alkaline solution was required to solidify waste oil to a practical hardness with a certain amount of solidification agent in the solution-type solidification agent. In other words, since the reactivity between the waste oil and the dispersant is poor, an excessive amount of a high-concentration alkaline solution is required. Further disadvantages of this solution-type high-concentration alkaline solution solidifying agent include safety problems at the time of skin contact due to high alkali concentration and corrosiveness to cooking utensils such as tempura pans. .

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 ベた結果、 固化が不十分であるある事が分かった。  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.

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力 リ溶液とてんぷ ら油との接触面積が小さ くそのために婊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 2 0〜 4 0 %の高濃度) 。 つま り、 従来の 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が油処理剤添加後の 撹拌のみによってしか行われず廃油中で粒子状にあるアル力リ 成分の粒子径が大きく なり、 そのためにアルカリ溶液と廃油と の接触面積が小さ く なる。 Therefore, the present inventors have conducted intensive studies on these causes, and as a result, the conventional solution-type solidifying agent is a uniform liquid as a whole, and when this is mixed with edible oil in a container such as a tempura pan, The artificial mixing with chopsticks and spatula etc. by housewives or workers etc. does not sufficiently mix the treatment agent and edible oil, and the contact area between the alkaline solution and the tempura oil is small. Reaction rate is low I inferred. In order to solve this, it has been necessary to add an excessive amount of alkali or to make the concentration too high (for example, a high concentration of 20 to 40% based on the entire treatment agent). In other words, in the conventional solution type dispersant, 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, and the waste oil is not used. The particle size of the particulate component increases, which reduces the contact area between the alkaline solution and the waste oil.

このよ うな問題点に対処し、 本発明では、 油処理剤を W/0型ェ マルシヨ ンと し、 はじめからアルカ リ溶液を微小粒子で分散さ せることにより、 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ものである。  In order to address such problems, the present invention uses a W / 0 emulsion as the dispersant and disperses the alkaline solution with fine particles from the beginning, so that the waste oil and the alkaline solution can be slightly stirred. This ensures a large contact area with the device.

このよ うなエマルショ ン型の油処理剤では、 アル力リを W/0型 エマルショ ンの液滴中に閉じこめることによ り、 処理剤中のァ ルカリ濃度を下げても十分な固化性能が得られる。 すなわち、 廃油に本油処理剤を用いると、 微少なアルカ リ溶液の粒子が分 散して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、 匕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 such emulsion type dispersants, sufficient solidification performance can be obtained even if the alkali concentration in the dispersant is reduced, by confining the alcohol in the droplets of the W / 0 type emulsion. Can be In other words, when the present dispersant is used for waste oil, fine alkaline solution particles disperse and the contact area with the waste oil increases drastically as compared with the conventional dispersant, and the reaction speed of the dagger increases. . Thus, the amount of alkali used can be reduced, and the risk of the user coming into contact with the dispersant or the cooking utensil containing waste oil is reduced.

こ こで、 上述の油処理剤について、 より詳しく説明すると、 本発明による油処理剤は、 アルカ リ の水 アルコール溶液をこ 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/0型) エマルシヨ ンである油処理剤を提供するこ とを要旨とするものある。 すなわち、 分散相と しては、 アル力 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、 連 続相には鉱物油や合成油などのいわゆるオイルが用いられる。 Here, the dispersant described above will be described in more detail.The dispersant according to the present invention is obtained by mixing and stirring a solution of an alcohol in water and alcohol with a solution having no or low compatibility with the solution. The gist is to provide a dispersant that is a water-in-oil type (W / 0 type) emulsion. In other words, the dispersed phase A mixed solution of the two is used. In addition, the continuous phase must be a liquid base material that does not dissolve in the dispersed phase components (that is, is incompatible or small). Further, preferably, since the solidification rate can be increased by being easily mixed with the waste oil, so-called oil such as mineral oil or synthetic oil is used for the continuous phase.

すなわち、 連続相の好ましい例と しては、 鉱物油、 合成油を 用いることが好ましく 、 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ーテル油、 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イ 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, a mineral oil or a synthetic oil is preferably used, and one or a mixture of two or more may be used. In the case of a mineral oil, a highly refined white oil is used. Is also good. For example, mineral oils such as lubricating base oils such as spindle oil, transformer oil, neutral oil, bright stock oil, and fuel oils such as petroleum naphtha, gasoline, kerosene, light oil, process oil, and synthetic oil Synthetic oils such as synthetic ester oils, synthetic ether oils, synthetic polyalkylene glycol oils, synthetic polyalphaolefins, alkylbenzene oils, and silicon oils.

さ らに、 連続相の W/0エマルシヨ ン全体に対する連続相の比と しては、 特に制限はないが、 4 0〜 9 5 %程度の連続相を用い るのが好ましい。  Further, the ratio of the continuous phase to the whole W / 0 emulsion is not particularly limited, but it is preferable to use a continuous phase of about 40 to 95%.

また、 分散相の中のアルカ リ成分と混合する水または水とァ 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 o  Further, there is no particular limitation on the ratio of water or water and alcohol or alcohol to be mixed with the alkaline component in the dispersed phase, but the alkaline component: water: alcohol = 3: 3: 7 is particularly preferred. Preferred o

また、 分散相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。 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 alkali used for the dispersed phase is not particularly limited as long as it is a strong alkali, but sodium hydroxide, potassium hydroxide, lithium hydroxide, barium hydroxide and the like are used. Preferably, sodium hydroxide is used. As the metal alkoxide used in the present invention, sodium alkoxide is preferable, and sodium ethoxide, sodium methoxide or a mixture thereof is used.

また、 分散相のアルカ リ溶液のアルカリ濃度と しては、 3 〜 6 0 %程度の濃度が好ま しく 、 さ らに好ましく は 3 0 %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 : アルコーノレ : = 2 0 〜 4 0 : 6 0 〜 8 0程 度が好ましい。  Further, as the alkali concentration of the alkaline solution of the dispersed phase, a concentration of about 3 to 60% is preferable, and a concentration of about 30% is more preferably used. The ratio of water to alcohol is not particularly limited, but is preferably about water: alconore: = 20 to 40:60 to 80.

また、 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 、 1 5 /Λ ΙΙΙ以下のものが用いられ、 好ましく は 1 0 / m 以下、 さ らに好ましく は 3 // m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、 エマルシヨ ンと しての分散安定 性が悪く なる。  The particle size of the alkaline mixed solution as the disperse phase is not particularly limited, and a particle size of 15 / Λ or less is used, preferably 10 / m or less, and more preferably 3 / m 2 or less. / m or less is good. If the particle size is large, the reactivity is reduced, and the dispersion stability as an emulsion is deteriorated.

また、 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、 力オリ 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。  In addition, it is not denied that powder is used as a component of the dispersant for increasing the amount or diluting the alkali concentration.For example, calcium hydroxide, calcium sulfate, bentonites, olizonites, etc. Carbonaceous particles such as perlite or carbon black or activated carbon may be mixed.

また、 本発明の油処理剤は、 W/0エマルシヨ 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、 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。 In the dispersant of the present invention, in order to form a W / 0 emulsion, a surfactant can be preferably used as a dispersant for dispersing an alkaline mixed solution in an oil component. When the dispersant is not used, the dispersant may be vigorously stirred at the time of use (immediately before the dispersant of the present invention is added to the waste oil) and then added to the waste oil. For example, if the dispersant is of a type that is filled into a bottle for each use, shaking the entire bottle saves time for stirring. It is preferable as it is not inconvenient.

また、 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、 ポリオレフイ ンアミ ド系またはその誘導体、 アル キル/アルケニルァミン系、 またはその誘導体、 ポリオレフィ ンアミ ドアルケンァミ ン系またはその誘導体、 ポリオキシェチ レン系、 ポリオキシフエニルエーテル系、 アルカリ金属および アルカ リ土類金属石鹺系の界面活性剤を 1種または 2種以上を 用いることができる。  The surfactant is not particularly limited as long as the dispersed phase can be stably dispersed in the continuous phase for a long time, but the properties of the continuous phase oil, the concentration of the dispersed phase, and the like are not limited. The type and amount of use may be appropriately adjusted in consideration of such factors.For example, polyalkenyl succinic acid imide or its derivative, polyalkenyl succinic acid amide or its derivative, polyolefin amide or its derivative, alkyl / One or two surfactants based on alkenylamines or their derivatives, polyolefinamide alkenamines or derivatives thereof, polyoxyethylene, polyoxyphenyl ether, alkali metal and alkaline earth metal stones The above can be used.

上記のよ うに構成された油処理剤によって例えば家庭で使用 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, for example, tempura oil used at home is treated with the dispersant configured as described above, the dispersant of the present invention is added to waste oil at around room temperature and stirred. Then, the waste oil and the dispersant immediately start reacting and solidify in about 1 minute, so they can be separated from the pot and discarded.

すなわち、 本発明の油処理剤は、 アルカ リ の水酸化物または アルカ リ混合溶液の分散相を有する W /0型エマルシヨ ンと したの で、 廃油に添加された際に、 微少で無数のアルカ リ の粒子が廃 油中に分散し、 験化の反応を開始する。 この場合、 本油処理剤 は微少で無数のアル力リ を廃油中に均一に分散させることがで き、 しかも、 上記アルカ リは液滴であるので、 少量のアルカリ 溶液で、 廃油とアルカ リ溶液の接触面積を充分に確保すること が出来、 速やかに廃油を固化して処理できる。 次に、 本発明による油処理剤の具体的な実施例について説明 する。 なお、 本発明は以下の実施例に限定されるものではない。 That is, the dispersant of the present invention is a W / 0 type emulsion having a dispersed phase of an alkali hydroxide or an alkali mixed solution. The particles are dispersed in the waste oil and initiate the experimental reaction. In this case, the dispersant can uniformly disperse minute and innumerable alcohols in the waste oil, and since the above-mentioned alkali is a droplet, a small amount of an alkaline solution can be used to dispose the waste oil and the alkali. The contact area of the solution can be sufficiently secured, and the waste oil can be quickly solidified and treated. Next, specific examples of the dispersant according to the present invention will be described. Note that the present invention is not limited to the following examples.

ここで、 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。  Here, in the examples, the results of comparison of the performance of the dispersant according to the present invention and the dispersant according to the prior art will be described using four evaluation test methods.

[評価試験法 1 ]  [Evaluation test method 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 一) 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つ て固化の程度が確認できるものである。  Use a commercially available glass beaker and a magnetic stirrer (Magnetic Stirrer I). The magnetic stirrer used was one whose rotation speed of the stirrer could be read directly by LED display. (Model: Iuchi Seieido Model No. HS-500 output 100V, 0.5A) According to this magnetic stirrer, when the contents in the beaker start to solidify, the viscosity increases and the load on the stirrer increases. If it is increased, the rotation speed decreases. The degree of reduction in the rotational speed differs depending on the degree of solidification, and the more solidified, the lower the rotational speed. In other words, the degree of solidification can be confirmed by observing the situation of the decrease in the rotational speed.

試験においては、 まず、 100mlのパイ レックスガラス製ビーカ 一中に食用油の廃油 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一中に加え、 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. Place a Teflon-coated magnetic stirrer in this and stir at room temperature. Set the rotation speed to 450 rpm ± 10 rpm before adding dispersant. Next, the test dispersant is added to the beaker, and the number of revolutions of the stirrer is immediately read to observe and record the change over time.

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 20r pm ( 1分間に 2 0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、 及ぴ固化時間を求めた。 [評価試験法 2 ] According to this test method, the dispersant having excellent solidification performance rapidly solidifies because the solidification occurs in a short time. The solidification criteria were 20 rpm (20 revolutions per minute), and the required amount of alkali (sodium hydroxide) in terms of solidification required and the solidification time were determined. [Evaluation test method 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 100ml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 2 7 cm<i»、 深さ 約 5 cm)  In a tempura pan at room temperature, add 600 ml of waste oil (room temperature) of tempura oil. Immediately after adding 100ml of dispersant, mix well with chopsticks for 1 minute and then leave. During this time, measure the time until solidification starts and the time required for solidification. (The size of the tempura pot is about 27 cm in diameter <i »and about 5 cm in depth.)

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ァ 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。  According to this test method, the amount of alkali (sodium hydroxide) required to solidify a predetermined amount of tempura oil was determined, and the difference between the dispersant according to the present invention and the dispersant according to the prior art was evaluated. I do.

<実施例 1 〜 4及び比較例 1 > <Examples 1 to 4 and Comparative Example 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 (45 g )のてんぶ ら油の廃油を固化するに要した油処理剤の量、 及び正味アル力 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 (〇印) と評価し、 表 2に記載した。 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) The amount of dispersant required to solidify the waste oil of the balance oil and the net amount of sodium hydroxide (sodium hydroxide) were determined. In addition, when it reached 20 rpm or less within 5 minutes, it was evaluated as solidification (marked with 、) and described in Table 2.

(表 1 ) 誦 2 綱 3 実删 4 比■ 化ナトリウム 10 8 6 5 17 水 10 8 6 5 33 エタノール 20 18 13 11 7 ニュートラ Jレ)由 60 66 75 79 腕性剤 (ポリアルケ二ルビス琥珀 イミド) 1.5 1.5 1.5 1.5 1.5 ジエチレングリコールモンイソブチルエーテル 20 プロピレングリコール 20(Table 1) Recitation 2 Class 3 Practice 4 Comparison Sodium chloride 10 8 6 5 17 Water 10 8 6 5 33 Ethanol 20 18 13 11 7 Neutral J) 60 60 75 79 Arming agent (Polyalkenyl bis-amber imide) ) 1.5 1.5 1.5 1.5 1.5 Diethylene glycol mon isobutyl ether 20 Propylene glycol 20

30%ラウリルアミン才キシド水溶 3 (表 2 ) 30% laurylamine oxidized water-soluble 3 (Table 2)

Figure imgf000015_0001
上記表 1及び 2 の通り、 実施例 1 〜 4 の油処理剤では 50mlの廃 油を固化するのに要する水酸化ナ ト リ ゥムの量は 0. 36〜0. 40 g であった。 これに対し比較例 1 では 2. 5 g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 ( 1ノ 5以下) の水 酸化ナ ト リ ゥムの使用量ですむことが確認された。
Figure imgf000015_0001
As shown in Tables 1 and 2, in the dispersants of Examples 1 to 4, the amount of sodium hydroxide required to solidify 50 ml of waste oil was 0.36 to 0.40 g. On the other hand, in Comparative Example 1, the weight was 2.5 g or more. Thus, it was confirmed that one-third (1-5 or less) of the amount of sodium hydroxide used was smaller than that of the conventional dispersant.

ぐ実施例 5〜 7 > Examples 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/0エマルショ ンを得てこれを用いた。  Sodium hydroxide is dissolved in a mixed solution of water and ethanol to obtain a solution to be used for the dispersed phase, added to the continuous phase, and stirred vigorously immediately before pouring into waste oil to obtain a W / 0 emulsion. This was used.

<実施例 8 〜 : L 3 〉 <Example 8-: L 3>

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/0エマルシヨ ンである油処理剤を得た。  Dissolve sodium hydroxide in a mixed solution of water and ethanol to obtain a solution to be used for the dispersed phase, and disperse it in the continuous phase using a surfactant as a dispersant to treat the oil as a W / 0 emulsion. Agent was obtained.

実施例 5〜 1 3 (成分組成は表 3 に示す通り。 単位は(g) ) お ょぴ後述の比較例 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〜 1 3及び比較例 2〜 6の評価を表 5にまとめ た。 Examples 5 to 13 (Ingredient composition is as shown in Table 3. The unit is (g)). Comparative Examples 2 to 6 described below (Ingredient composition is as shown in Table 4. The unit is (g)). By applying Evaluation Test Method 2, the solidification performance of the waste oil, which is the effect of the dispersant of the present invention, was evaluated for the ease of mixing, the solidification state, and the solidification rate. Observe and clarify the difference from the conventional technology by the following evaluation criteria. Table 5 summarizes the evaluations of Examples 5 to 13 and Comparative Examples 2 to 6.

[廃油との混合の容易性]  [Ease of mixing with waste oil]

◎ ; 特に混合しゃすい ◎ : Especially mixed

〇 ; 混合しゃすい 混合; Mixed

△ ; やや混合しにく い △: Somewhat difficult to mix

X ; 混合しにく レヽ X;

[固化状態]  [Solidified state]

◎ ; 全体的に均一に固化 ◎; solidified uniformly throughout

〇 ; ほぼ全体的に固化。 一部柔らかい部分有り。  〇; Almost solidified. Some soft parts.

△ ; 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.

X ; 固化しない。 X: does not solidify.

[固化速度]  [Solidification speed]

◎ ; 適度な速度で固化。 A: solidified at an appropriate speed.

〇 ; ゆっく り と固化。 〇; Solidified slowly.

△ ; 固化速度が速過ぎ部分的に固化。 Δ: The solidification speed was too high and the solidification was partially achieved.

X ; 固化しない。 X: does not solidify.

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。 分散相 連翩 分散剤 If 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. It means that it cannot be processed. Disperse phase

水^化ナトリウム 水 エタノール  Sodium hydrate Water Ethanol

辦 i 5 8 8 20 トランス油 64  辦 i 5 8 8 20 Transformer oil 64

辦 J 6 8 8 20 ニュ一卜ラル油(低粘度) 64  辦 J 6 8 8 20 Neutral oil (low viscosity) 64

鋼 7 8 8 20 ニュ一卜ラル油( 度) 64  Steel 7 8 8 20 Neutral oil (degree) 64

雄例 8 8 8 20 卜ランス油 63 ポリアルケ-ニルビス琥珀 ¾イミド(低分子型) 1 en 鋼 9 8 8 20 ニュ -卜ラル油(低粘度) 63 ポリアルケ-ニルビス琥珀 ^イミド (低分子型) 1 遍 1 0 8 8 20 ニュ一卜ラル油(高粘度) 63 ポリ 7ルケ-二ルビス號 ¾ イミド(低分子型) 1 遍 1 1 8 8 20 トランス油 63 ポリアルケ.二ルビス號 ¾ イミド(高分子型) 1 辦 1 2 8 8 20 ニュ一卜ラル油(低粘度) 63 ポリ 7ルケ.二ルビス號 ¾酸イミド(高分子型) 1 鋼 1 3 8 8 20 ニュ -卜ラル油(勰度) 63 ポリアルケ.二ルビス ί虎 ¾ イミド(高分子 1  Male example 8 8 8 20 Trans-oil 63 Polyalkenyl-nyl bis-amber imide (low molecular type) 1 en Steel 9 8 8 20 Neutral oil (low-viscosity) 63 Polyalkenyl-nyl bis-amber ^ imide (low molecular type) 1 Hen 1 0 8 8 20 Neutral oil (high viscosity) 63 Poly 7Luke-Nilbis No. ¾ Imide (low molecular type) 1 Hen 1 1 8 8 20 Trans oil 63 Polyalkene.Nilbis No. ¾ Imide (Polymer Type 1 辦 1 2 8 8 20 Neutral oil (low viscosity) 63 Poly 7L.2Rbis No. Acid imide (polymer type) 1 Steel 1 3 8 8 20 Neutral oil (勰 degree) 63 Polyalkene.2rubis ίtiger ¾ imide (polymer 1

) 03 来技術の油処理剤について下記のとおり試験した。 ) 03 The state of the art dispersants were tested as follows.

く比較例 2〜 3 > Comparative Examples 2-3>

水酸化ナ ト リ ゥ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/レ、 ジエチレングリ コーノレモノイ ソブチノレエー テル、 ラウリ ルアミンォキシ 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。  To a solution of sodium hydroxide in water, add a mixed solution of propylene glycol, ethanol / re, diethyleneglycone monomonosobutinoether, and aqueous solution of laurylamine oxide, and apply a uniform liquid dispersant. Obtained.

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.

<比較例 4〜 5 > <Comparative Examples 4 to 5>

水酸化ナ ト リゥムを水に溶解したものに、 2-フエノキシエタ ノ ーノレ、 ポリ プロ ピレングリ コール、 イ ソプロ ピノレアルコール、 ラウリルアミンォ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。  To a solution of sodium hydroxide dissolved in water, add a mixed solution of 2-phenoxyethanol, polypropylene glycol, isopropynole alcohol, and aqueous solution of laurylamine oxide, and apply a uniform liquid dispersant. Obtained.

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.

ぐ比較例 6 > Comparative Example 6>

表 4に示すとおり 12-ヒ ドロキシステアリ ン酸 15gを比較例 6 の油処理剤と した。 なお、 12 -ヒ ドロキシステアリ ン酸の性状は 粉末であった。  As shown in Table 4, 15 g of 12-hydroxycystearyl acid was used as the dispersant in Comparative Example 6. The properties of 12-hydroxycystearyl acid were powder.

(表 4 )  (Table 4)

腿例 2 誦 3 顯 4 比綱 5 比删 6 Thigh example 2 Reciting 3 Akira 4 Higa 5 Hira 6

*i化ナトリウム 8.0 16.7 8.0 18.4 * Sodium iodide 8.0 16.7 8.0 18.4

水 16.0 33.3 16.0 36.8  Water 16.0 33.3 16.0 36.8

エタノール 3.2 6.7  Ethanol 3.2 6.7

2—フエノキシエタノール 10.0 24.0  2-phenoxyethanol 10.0 24.0

イソプロビルアルコール 2.7 6.1 プロピレングリコール 9.6 20.0  Isopropyl alcohol 2.7 6.1 Propylene glycol 9.6 20.0

ポリプロピレングコール 5.2 12.3  Polypropylene glycol 5.2 12.3

ジェチレングリコールモンィソブヂルエーテル 9.6 20.0  Detylene glycol monisobutyl ether 9.6 20.0

30%ラウリルアミン才キシド水溶 3.3 3.3 3.3 3.3  30% laurylamine aqueous oxide 3.3 3.3 3.3 3.3

12—ヒドロキシステアリン ¾ 15.0 (表 5 ) 12-hydroxystearin ¾ 15.0 (Table 5)

Figure imgf000019_0001
Figure imgf000019_0001

上記の通り、 実施例 5 〜 1 3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。  As described above, Examples 5 to 13 are easier to mix than the dispersants of Comparative Examples 2 to 6, solidification proceeds at an appropriate speed, and the waste oil can be uniformly solidified as a whole. Was.

<実施例 1 4及び比較例 7 > <Example 14 and Comparative Example 7>

[評価試験方法 3 ]  [Evaluation test method 3]

固化した廃油の固さを調べる基準と して、 直径 2 c m、 重量 6 gのガラス球を固化した廃油上に静置し、 1 0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。  As a standard for examining the hardness of the solidified waste oil, a glass ball having a diameter of 2 cm and a weight of 6 g was allowed to stand on the solidified waste oil, and after 10 minutes, the sedimentation distance was measured. In addition, the method of visual observation and disposal will be confirmed, and the difference from the conventional technology will be clarified.

実施例 1 4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及ぴ比較例 7の評価を表 7に まとめた。 (表 6 )

Figure imgf000020_0001
In Example 14 and Comparative Example 7 (the composition of the components is as shown in Table 6. The unit is (g)), the evaluation test method 3 was applied, and the hardness of the waste oil after solidification was observed. Table 7 summarizes the evaluations of Example 14 and Comparative Example 7. (Table 6)
Figure imgf000020_0001

(表 7 )(Table 7)

Figure imgf000020_0002
上記の通り実施例 1 4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。
Figure imgf000020_0002
As described above, it was confirmed that in Example 14, compared with the dispersant of Comparative Example 7, the waste oil could be solidified as a whole, and the oil could be easily disposed of because no oil remains.

ぐ実施例 1 5 〜 1 7 > Examples 15 to 17>

[評価試験方法 4 ]  [Evaluation test method 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 2 0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。 実施例 1 5〜 1 7の成分組成及ぴ攪拌機の回転数、 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第 1図に示すグラ フを用いて説明する。 The dispersant is prepared by first preparing a mixed solution of sodium hydroxide and alcohol, which are the dispersed phases, and dropping it into the continuous phase mineral oil to which the surfactant has been added in advance. Stirred for 20 minutes. At the time of stirring, the diameter of the dispersed phase particles was changed in three stages by adjusting the rotation speed of the stirrer. The particle diameter was measured by microscopic observation and photographing, and the average particle diameter was measured and confirmed. With this evaluation method, the relationship between the particle size of the dispersed phase and the solidification rate was confirmed. Table 8 shows the component compositions, the rotation speeds of the stirrers, and the particles of Examples 15 to 17. Table 9 shows the results of tests using the above evaluation method 4. The solidification state will be described with reference to Table 9 and the graph shown in Fig. 1.

(表 8 ) 綱 15 誦 16 謹 17 水 化ナトリウム 8.0g  (Table 8) rope 15 recitation 16 grace 17 sodium hydride 8.0g

分散相 水 8.0g  Dispersed phase water 8.0g

エタノール 18.7g  18.7 g of ethanol

翻 ニュー卜ラル油  Neural oil

分散剤 ポリアルケニルビス琥珀酩イミド 1.5g  Dispersant 1.5 g of polyalkenyl bis amber lanimide

撤權の回!^ (rpm) 1500 600 200 分散相の の平均 δ子径( m) 3 以下 5~ 15/m 15 以上 Time of withdrawal! ^ (Rpm) 1500 600 200 Average diameter of dispersed phase δ diameter (m) 3 or less 5 ~ 15 / m 15 or more

(表 9 ) (Table 9)

Figure imgf000022_0001
里 ( r pm)
Figure imgf000022_0001
Village (r pm)

上記表 8、 表 9、 第 1 図よ 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。 産 業 上 の 利 用 可 能性  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. Industrial availability

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 above, the oil dispersant according to the present invention can solidify waste oil at around normal temperature, and is easily mixed with waste oil. It has various effects such as reducing the use of strong alkaline.

Claims

請 求 の 範 囲 The scope of the claims 1 . 油性の連続相に水性の分散相が分散されてなる W/0型ェマル ショ ンの油処理剤であつて、 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力 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/0型エマルシヨ ンであるこ とを特徴とする油処 理剤。 1. A W / 0 emulsion dispersant comprising an aqueous continuous phase dispersed in an oily continuous phase, wherein the dispersed phase contains water, a solution containing water and alcohol, or contains water. A mixed solution of an alkali solution and a hydroxide of an alkali such as sodium hydroxide or a metal alkoxide such as a sodium alkoxide. Is a W / 0 emulsion comprising the dispersed phase and a liquid having no compatibility. 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/0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 oil treating agent according to claim 1, wherein the dispersant for dispersing the dispersed phase in the continuous phase is a W / 0 emulsion using a surfactant. 3 . 前記分散相の粒子の径を 1 5 /Z m以下と したことを特徴とす る請求項 2 に記載の油処理剤。 3. The dispersant according to claim 2, wherein the diameter of the particles of the dispersed phase is 15 / Zm or less. 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、 ポリオレフイ ンア ミ ド系またはその誘導体、 アルキル アルケ ニルァ ミ ン系またはその誘導体、 ポ リ オレフイ ンア ミ ドアルケ ンァ ミ ン系またはその誘導体、 ポリ オキシエチレン系、 ポリオ キシフエニルエーテル系、 アル力 リ金属およびアルカ リ土類金 属石鲮系の界面活性剤を 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 surfactant is a polyalkenyl succinic amide or a derivative thereof, a polyalkenyl succinic amide or a derivative thereof, a polyolefin amide or a derivative thereof, an alkyl alkenyl amide or a derivative thereof, One or two surfactants based on polyolefin amide alkenamine or its derivatives, polyoxyethylene, polyoxyphenyl ether, alkali metal and alkaline earth metal stone What we use 3. The dispersant according to claim 2, wherein: 5 . 前記分散相の粒子の径を 1 5 /z m以下と したことを特徴とす る請求項 1 に記載の油処理剤。 5. The dispersant according to claim 1, wherein the particle size of the dispersed phase is 15 / zm or less. 6 . 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。 6. The dispersant according to claim 1, wherein the continuous phase is a mineral oil or a synthetic oil. 7 . 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 アルファオレフイ 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 6に記載の油処理剤。 7. The continuous phase is a mineral oil, such as spindle oil, trans oil, neutral oil, bright stock oil, lubricating base oil, or fuel naphtha, gasoline, kerosene, or gas oil. , Process oils, liquid paraffin, synthetic ether oils that are synthetic oils, synthetic polyalkylene glycol oils, synthetic polyalphaolefins, alkylbenzene oils, and silicon oils1 7. The dispersant according to claim 6, wherein the dispersant is obtained by using one or more kinds of oil components. 8 . 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、 ォレフィ 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 mの粒子と して前記連続相に分散させてなる W/0型エマ ルショ ンであることを特徴とする油処理剤。 8. It is selected from a dispersed phase consisting of a mixed solution of water and ethanol in which sodium hydroxide is dissolved, and a paraffinic hydrocarbon, an olefinic hydrocarbon, or an aromatic hydrocarbon having a flash point of 50 or more. One or more continuous phases and a W / 0 type emulsion obtained by dispersing the dispersed phase as particles having a particle size of approximately m with a surfactant in the continuous phase. Dispersant. 9 . 前記分散相が、 水酸化ナ ト リ ウム 2〜30%、 水 1〜40%、 エタ ノール 2〜80¾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。 9. The dispersed phase is 2-30% sodium hydroxide, 1-40% water, ethanol 2. The dispersant according to claim 1, wherein the dispersant comprises 2-80% of knol, and the continuous phase is a mineral oil.
PCT/JP1999/001015 1998-03-06 1999-03-03 Treating agent for oil Ceased WO1999045086A1 (en)

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Citations (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

Patent Citations (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

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