JP2005530862A - Fuel additive - Google Patents

Fuel additive Download PDF

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JP2005530862A
JP2005530862A JP2003574227A JP2003574227A JP2005530862A JP 2005530862 A JP2005530862 A JP 2005530862A JP 2003574227 A JP2003574227 A JP 2003574227A JP 2003574227 A JP2003574227 A JP 2003574227A JP 2005530862 A JP2005530862 A JP 2005530862A
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composition
fuel
naphtha
hydrocarbon fuel
water
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モーズリー,マイケル,ジョン
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ハイドロフューエル (プロパリエトリー) リミテッド
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • A61P31/06Antibacterial agents for tuberculosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
    • C09K23/017Mixtures of compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/32Liquid carbonaceous fuels consisting of coal-oil suspensions or aqueous emulsions or oil emulsions
    • C10L1/328Oil emulsions containing water or any other hydrophilic phase
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/02Use of additives to fuels or fires for particular purposes for reducing smoke development
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/04Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/06Use of additives to fuels or fires for particular purposes for facilitating soot removal
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/12Inorganic compounds
    • C10L1/1233Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof
    • C10L1/125Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/16Hydrocarbons
    • C10L1/1616Hydrocarbons fractions, e.g. lubricants, solvents, naphta, bitumen, tars, terpentine
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/188Carboxylic acids; metal salts thereof
    • C10L1/1881Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/192Macromolecular compounds
    • C10L1/198Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
    • C10L1/1985Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/222Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/224Amides; Imides carboxylic acid amides, imides

Abstract

エトキシル化アルキルフェノール、脂肪酸アミド、ナフサおよびオレイン酸を含有する乳化性組成物。前記組成物は内燃機関、開放炎バーナ(ボイラ類)あるいは類縁物において燃料と水の混合物を乳化するのに用いられる。好ましくは前記組成物は、体積でポリオキシエチレンノニルフェノール1部、ココナッツジエタノールアミド2部、ヘビーナフサ2部、およびオレイン酸1部を含有する。本発明はさらに、本発明の組成物を含有する炭化水素燃料、および前記組成物を含有する炭化水素燃料と水との乳化物を生成する方法にも及ぶ。An emulsifiable composition comprising an ethoxylated alkylphenol, a fatty acid amide, naphtha and oleic acid. The composition is used to emulsify fuel and water mixtures in internal combustion engines, open flame burners (boilers) or the like. Preferably, the composition contains, by volume, 1 part polyoxyethylene nonylphenol, 2 parts coconut diethanolamide, 2 parts heavy naphtha, and 1 part oleic acid. The invention further extends to a hydrocarbon fuel containing the composition of the invention and a method for producing an emulsion of a hydrocarbon fuel containing the composition and water.

Description

本発明は燃料に関する。特に、乳化性組成物、炭化水素燃料、および炭化水素燃料と水との乳化物の生成方法に関する。   The present invention relates to fuel. In particular, the present invention relates to an emulsifiable composition, a hydrocarbon fuel, and a method for producing an emulsion of a hydrocarbon fuel and water.

本発明によれば
エトキシル化アルキルフェノール;
脂肪酸アミド;
ナフサ;および
オレイン酸
を含有する乳化性組成物が提供される。
According to the invention, ethoxylated alkylphenols;
Fatty acid amides;
An emulsifiable composition comprising naphtha; and oleic acid is provided.

エトキシル化アルキルフェノールは一般式R(OCH2CH2nOHで表される非イオン界面活性剤である。ここでRはアルキルフェノール、nはエトキシ基の数を表す。 Ethoxylated alkylphenols are nonionic surfactants represented by the general formula R (OCH 2 CH 2 ) n OH. Here, R represents alkylphenol, and n represents the number of ethoxy groups.

エトキシル化アルキルフェノールの例としてはポリオキシエチレン(POE)ノニルフェノールがあり、たとえばICI社からSYNPERONIC NPの商品名で入手可能な商品が例示される。本発明の好ましい実施形態としてPOE(5)あるいはPOE(6)ノニルフェノール(たとえばSYNPERONIC NP5あるいはSYNPERONIC NP6)を用いることができる。   An example of an ethoxylated alkylphenol is polyoxyethylene (POE) nonylphenol, for example, a product available from ICI under the trade name SYNPERONIC NP. POE (5) or POE (6) nonylphenol (for example, SYNPERONIC NP5 or SYNPERONIC NP6) can be used as a preferred embodiment of the present invention.

脂肪酸アミドは脂肪酸ジアルカノールアミドでよい。本発明の好ましい実施形態としては脂肪酸アミドはココナッツジエタノールアミド、たとえばアルブライトアンドウィルソン社より商品名EMPILAN2502という商品名で入手できるものが用いられる。   The fatty acid amide may be a fatty acid dialkanolamide. In a preferred embodiment of the present invention, the fatty acid amide is coconut diethanolamide, such as that available from Albright & Wilson under the trade name EMPILAN2502.

ナフサはヘビーナフサでよい。   The naphtha may be heavy naphtha.

本発明の好ましい実施形態においては前記組成物はポリオキシエチレンノニルフェノール、ココナッツジエタノールアミドおよびヘビーナフサを含有することができる。好ましくは前記組成物は体積でポリオキシエチレンノニルフェノール1部、ココナッツジエタノールアミド2部、ヘビーナフサ2部およびオレイン酸1部を含有することができる。   In a preferred embodiment of the present invention, the composition may contain polyoxyethylene nonylphenol, coconut diethanolamide and heavy naphtha. Preferably, the composition may contain, by volume, 1 part polyoxyethylene nonylphenol, 2 parts coconut diethanolamide, 2 parts heavy naphtha and 1 part oleic acid.

本発明はさらに本発明による組成物を含有する炭化水素燃料に拡張される。   The invention further extends to hydrocarbon fuels containing the composition according to the invention.

前記炭化水素燃料はアルコール系の燃料、ガソリン(ぺトロール)、ディーゼル燃料、たとえば低硫黄ディーゼル油、またはその混合物でよい。   The hydrocarbon fuel may be an alcohol-based fuel, gasoline (petrol), diesel fuel, such as low sulfur diesel oil, or a mixture thereof.

炭化水素燃料は体積で40%以下の水を含有することができる。好ましくは炭化水素燃料は25%以下の水を含有することができる。   The hydrocarbon fuel can contain up to 40% water by volume. Preferably, the hydrocarbon fuel can contain up to 25% water.

炭化水素燃料は前記組成物を体積で約1.5%ないし2%含有することができる。   The hydrocarbon fuel may contain about 1.5% to 2% of the composition by volume.

本発明の他の態様によれば、炭化水素燃料にエトキシル化アルキルフェノール、脂肪酸アミド、ナフサおよびオレイン酸を添加して混合物を形成し、ついで前記混合物に水を添加する、炭化水素燃料と水との乳化物の形成方法が提供される。   According to another aspect of the present invention, a hydrocarbon fuel and water are added to the hydrocarbon fuel by adding ethoxylated alkylphenol, fatty acid amide, naphtha and oleic acid to form a mixture, and then adding water to the mixture. A method of forming an emulsion is provided.

好ましくは前記方法はエトキシル化アルキルフェノール、脂肪酸アミド、オレイン酸およびナフサを含有する添加剤組成物を形成し、ついで前記添加剤組成物を炭化水素燃料に添加する方法を含む。   Preferably, the method includes forming an additive composition containing ethoxylated alkylphenol, fatty acid amide, oleic acid and naphtha, and then adding the additive composition to a hydrocarbon fuel.

好ましくは、体積でポリオキシエチレンノニルフェノール1部、ココナッツジエタノールアミド2部、オレイン酸1部およびヘビーナフサ2部を含有する組成物を炭化水素燃料に添加して前記混合物を形成する。   Preferably, a composition containing 1 part polyoxyethylene nonylphenol, 2 parts coconut diethanolamide, 1 part oleic acid and 2 parts heavy naphtha by volume is added to the hydrocarbon fuel to form the mixture.

前記添加物の成分はポリオキシエチレンノニルフェノール、ココナッツジエタノールアミド、オレイン酸およびナフサの順に混合し、前記組成物を形成するのが有利である。   The additive components are advantageously mixed in the order of polyoxyethylene nonylphenol, coconut diethanolamide, oleic acid and naphtha to form the composition.

本発明の組成物は、内燃機関、船舶ボイラ用途すなわち開放炎バーナや類似物などのための比較的コスト優位性の高い増量剤を提供することが、本発明の利点であると、本願出願人は考えている。前記組成物に用いられる成分は比較的安価に入手でき、しかも低温でも容易に混合可能である。4つの成分を適当に選ぶことにより、比較的少量の前記混合物の添加で燃料に多量の水(典型的には燃料:水=3:1)を加えても効果的な結果を得ることができる。本願出願人は、重質燃料から軽質燃料にわたって前記組成物の添加量はあまり変える必要がないと考えている。本願出願人は、最終的ブレンド物は安定な乳化物を形成し、持続期間中において沈降物の生じる気配がないということはさらなる本発明の長所であると考えている。   It is the applicant's benefit that the composition of the present invention provides a relatively cost-effective bulking agent for internal combustion engines, marine boiler applications, ie open flame burners and the like. Is thinking. The components used in the composition are available at a relatively low cost, and can be easily mixed even at low temperatures. By selecting the four components appropriately, it is possible to obtain an effective result even if a large amount of water (typically fuel: water = 3: 1) is added to the fuel by adding a relatively small amount of the mixture. . The applicant of the present application considers that the addition amount of the composition does not need to change much from heavy fuel to light fuel. Applicants believe that it is a further advantage of the present invention that the final blend forms a stable emulsion and that there is no sign of sedimentation during the duration.

本願出願人はまた、前記組成物は清浄な燃焼をもたらし、従って環境に優しい燃料を提供するものと考えている。前記組成物を含有しない燃料に比べて窒素酸化物、硫黄酸化物、一酸化炭素、二酸化炭素の濃度は削減される。さらに排気放出ガス中に明示されている酸素濃度および過剰空気がかなりの増加を示しており、また煤煙あるいは未燃焼炭素のかなりの削減も認められる。   Applicant also believes that the composition provides clean combustion and thus provides an environmentally friendly fuel. Concentrations of nitrogen oxides, sulfur oxides, carbon monoxide, and carbon dioxide are reduced compared to fuels that do not contain the composition. In addition, the oxygen concentration and excess air specified in the exhaust emissions show a significant increase, and a significant reduction in soot or unburned carbon is also observed.

本願出願人はまた、本発明による燃料は排気ガス温度を低下させる結果、エンジン寿命を延ばすものと考えている。   The Applicant also believes that the fuel according to the present invention extends engine life as a result of lower exhaust gas temperatures.

前記組成物が無臭で、酸性でなく、無毒性であり、従って付着しても皮膚に有害でないことは、本発明のさらなる長所である。さらに前記組成物の引火点は実質的に混合する燃料の引火点と同じなので、組成物を燃料に混入することによる取り扱いや輸送の際の安全性の考え方での妥協の必要はない。   It is a further advantage of the present invention that the composition is odorless, non-acidic, non-toxic and therefore not harmful to the skin when attached. Furthermore, since the flash point of the composition is substantially the same as the flash point of the fuel to be mixed, there is no need for compromise in terms of safety in handling and transportation by mixing the composition into the fuel.

本願出願人はまた、性能を最適化するために若干空気と燃料の流量を調節さえすれば通常の炭化水素燃料をそっくり前記組成物に置き換えることもできると考えている。   The Applicant also believes that conventional hydrocarbon fuels can be replaced by the above-described compositions as long as the air and fuel flow rates are slightly adjusted to optimize performance.

内燃機関は通常の燃料で運転していると炭素の蓄積や燃料に由来する他の析出物を経験する。本願出願人は、本発明の組成物を含有する燃料で運転するとこれらは分解して排出されるものと考えている。長期間運転してもエンジンの部品、特に燃料ポンプの部品には摩滅や腐食はなく、古いエンジンでもそれまでより滑らかに作動する。   Internal combustion engines experience carbon accumulation and other deposits derived from fuel when operating on normal fuel. The Applicant believes that when operating with a fuel containing the composition of the present invention, these are decomposed and discharged. Engine parts, especially fuel pump parts, will not wear out or corrode even after long periods of operation, and older engines will run more smoothly than before.

実施例2における試験において一定の回転数では本発明の燃料の方がディーゼル燃料に比較するとわずかに少ない燃料供給速度で済み、またその速度では出力は増加している。排気温度も有意に低下する。同じ出力で低速回転、低操作温度にするとエンジン寿命の延長に寄与すると考えられる。   In the test in Example 2, the fuel of the present invention requires a slightly lower fuel supply speed than the diesel fuel at a constant rotation speed, and the output increases at that speed. The exhaust temperature also decreases significantly. It is thought that if the same output is set at a low speed and a low operating temperature, the engine life is extended.

本願出願人はまた、前記組成物をタンカーで輸送する大量の燃料中に混入しておくと、石油流出災害の問題を軽減することができるものと考えている。組成物は乳化性を持っているので、水中での油膜形成の問題を軽減すると思われる。   The present applicant also believes that the problem of oil spill disaster can be reduced if the composition is mixed in a large amount of fuel transported by a tanker. Since the composition has emulsifying properties, it seems to reduce the problem of oil film formation in water.

次に本発明を以下の非限定的な実施例および試験例を参照して説明する。   The invention will now be described with reference to the following non-limiting examples and test examples.

ポリオキシエチレンノニルフェノール(SYNPERONIC NP5またはNP6)1部、ココナッツジエタノールアミド(EMPILAN2502)2部、オレイン酸1部およびヘビーナフサ2部を含有する、本発明による添加剤組成物のバッチを調整した。成分は上述の順序で混合した。1.8リットルの前記バッチ組成物を71.79リットル(15.792英国ガロン)のベース炭化水素燃料に添加した。使用したベース燃料は体積でバンカーC油燃料70%とディーゼル燃料30%を含有するNo.5燃料油の70/30ブレンドであった。前記組成物とベース燃料の混合物を圧縮空気を用いて攪拌し、約2〜5分放置して前記組成物と前記燃料油の分散物を得た。その後、水23.93リットル(5.264ガロン)を前記混合物に添加した。得られた混合物を圧縮空気を用いて約2〜5分攪拌し前記燃料/水の乳化物とした。必要であれば20分後にもう一度攪拌してもよい。上記の体積量から分かるように、得られた混合物は最終ブレンド物中に水約25体積%と前記組成物約1.86体積%を含有していることになる。   A batch of an additive composition according to the present invention was prepared containing 1 part polyoxyethylene nonylphenol (SYNPERONIC NP5 or NP6), 2 parts coconut diethanolamide (EMPILAN2502), 1 part oleic acid and 2 parts heavy naphtha. The ingredients were mixed in the order described above. 1.8 liters of the batch composition was added to 71.79 liters (15.792 British gallons) of base hydrocarbon fuel. The base fuel used was No. 1 containing 70% Bunker C oil fuel and 30% diesel fuel by volume. A 70/30 blend of 5 fuel oils. The mixture of the composition and the base fuel was stirred using compressed air and left for about 2 to 5 minutes to obtain a dispersion of the composition and the fuel oil. Thereafter, 23.93 liters (5.264 gallons) of water was added to the mixture. The obtained mixture was stirred for about 2 to 5 minutes using compressed air to obtain the fuel / water emulsion. If necessary, it may be stirred again after 20 minutes. As can be seen from the above volume, the resulting mixture will contain about 25% by volume water and about 1.86% by volume of the composition in the final blend.

下記の試験のために、全域調整型工業燃焼用Hev−e−Oilバーナを装着した74.6KW(100馬力)のスコッチマリンボイラを使用した。前記ボイラは二つの供給源、すなわち上記の(添加剤なしの)No.5ブレンド燃料を入れた主タンクと実施例1に従って調製された燃料を入れた補助タンクとから、燃料を受け入れられるように改造した。ボイラの返送ラインのパイプを、それぞれ主燃料油ポンプおよびバーナバイパスバルブを通って再循環するように付け替えた。この改造によってボイラに供給する燃料を、返送油について考慮することなく、必要に応じて二つの供給源を切り替えられる。試験は上述のようなボイラと構成により、下記にさらに詳しく示すようにして行った。   For the following test, a 74.6 KW (100 hp) Scotch marine boiler equipped with a global adjustment type industrial combustion Hev-e-Oil burner was used. The boiler has two sources: No. 1 above (without additives). From the main tank containing the 5 blended fuel and the auxiliary tank containing the fuel prepared according to Example 1 was modified to accept the fuel. The boiler return line pipes were recirculated through the main fuel oil pump and burner bypass valve, respectively. With this modification, the fuel supplied to the boiler can be switched between two sources as needed without considering the return oil. The test was carried out as described in more detail below with the boiler and configuration described above.

試験例No.1
最初ボイラを主タンクに入れたNo.5燃料油でボイラの圧力が約344KPa(50ポンド/平方インチ(psi))になるまで運転した。この圧力に達した後、炎の初期点検のためにボイラの操作を実施例1に従って調製した燃料に切り替えた。円滑な移行が観測された。炎の輪郭は明確で、No.5の燃料油の炎よりも細く、長いものであった。ボイラは自動の全域調整モードで行った。ボイラは切り替え後の方が著しく静かであった。蒸気の圧力が約361.7Pa(52.5psi)に上昇するのも観測された。
Test Example No. 1
The first boiler was placed in the main tank. The fuel was operated at 5 fuel oil until the boiler pressure was about 344 KPa (50 pounds per square inch (psi)). After reaching this pressure, the boiler operation was switched to the fuel prepared according to Example 1 for an initial inspection of the flame. A smooth transition was observed. The outline of the flame is clear. It was thinner and longer than the fuel oil flame of No. 5. The boiler was operated in automatic full adjustment mode. The boiler was much quieter after switching. It was also observed that the vapor pressure rose to about 361.7 Pa (52.5 psi).

試験例No.2
実施例1に従って調製した燃料を用いてボイラに点火し約361.7KPa(52.5psi)となるように操作温度を上げていった。No.5燃料油と実施例1による燃料との比較を同一条件で行うために、ボイラは、手動モードで高火力位置付近に設定することにより、燃料/空気比リンク機構全ての位置を固定した。この運転中、ボイラを最適な効率となるようには設定しなかった。燃焼試験は両方の燃料について燃焼分析計Enerac2000を用い、二酸化炭素、一酸化炭素、可燃性ガス、過剰空気および酸素の排出を測定した。結果を下記の表1に示す。この試験結果では、本発明による燃料を用いた方が過剰空気と酸素が増加したにもかかわらず、二酸化炭素、一酸化炭素、および可燃性ガスの放出が減少していた。
Test Example No. 2
The boiler was ignited using the fuel prepared according to Example 1 and the operating temperature was raised to about 361.7 KPa (52.5 psi). No. In order to compare the five fuel oils and the fuel according to Example 1 under the same conditions, the boiler was fixed in the vicinity of the high thermal power position in the manual mode, thereby fixing the positions of all the fuel / air ratio link mechanisms. During this operation, the boiler was not set for optimum efficiency. The combustion test used a combustion analyzer Enerac 2000 for both fuels to measure carbon dioxide, carbon monoxide, combustible gas, excess air and oxygen emissions. The results are shown in Table 1 below. The test results showed that the emissions of carbon dioxide, carbon monoxide, and combustible gases were reduced when the fuel according to the present invention was used, although the excess air and oxygen increased.

試験例No.3
蒸気流量試験を行った。この試験を行うために水供給ポンプとボイラの間に流量計を設置した。ボイラを実施例1による燃料で運転し、操作圧約379KPa(55psi)にした。蒸気容量を無作為に測定し約832.6kg/時(1834ポンド/時)であった。この値はボイラに入る水の量を所定期間にわたってフローメータで測定し、ボイラ工業界により受け入れられている、蒸発した水の質量とガロンとの関係(すなわち蒸気の質量(ポンド/時)を500で割ったものが蒸発した水のガロン/分に相当する)により計算した。
Test Example No. 3
A steam flow test was performed. In order to perform this test, a flow meter was installed between the water supply pump and the boiler. The boiler was operated with the fuel from Example 1 and an operating pressure of about 379 KPa (55 psi). Vapor capacity was measured randomly and was about 832.6 kg / hr (1834 lb / hr). This value is determined by measuring the amount of water entering the boiler with a flow meter over a period of time, and the relationship between the mass of evaporated water and the gallon accepted by the boiler industry (ie the mass of steam in pounds per hour). (Corresponding to gallon / min of evaporated water).

試験例No.4
実施例1による燃料による蒸気流量をNo.5ブレンド油による蒸気流量と比較した。ボイラを手動モードにして炎を正しい位置に固定した。この試験の結果により、実施例1による燃料は、17分で約345.4リットル(76ガロン)の水が蒸発したことに基づいて1114.7kg/時(2235ポンド/時)の速度で蒸気を発生するのに対し、No.5燃料油は、15分で約295.4リットル(65ガロン)の水が蒸発したことに基づいて約983.8kg/時(2167ポンド/時)の速度で蒸気を発生することが示された。平均排気筒温度は、実施例1による燃料の場合は約265.6℃(510°F)で、No.5燃料油の場合は約246.1℃(475°F)と測定された。
Test Example No. 4
The steam flow rate by the fuel according to Example 1 is No. Compared to the steam flow with 5 blend oils. The boiler was in manual mode and the flame was fixed in the correct position. According to the results of this test, the fuel from Example 1 vaporized at a rate of 1114.7 kg / hr (2235 lb / hr) based on the evaporation of about 345.4 liters (76 gallons) of water in 17 minutes. No. 5 fuel oil was shown to generate steam at a rate of about 983.8 kg / hr (2167 lb / hr) based on the evaporation of about 295.4 liters (65 gallons) of water in 15 minutes. . The average exhaust stack temperature was about 265.6 ° C. (510 ° F.) in the case of the fuel according to Example 1, In the case of 5 fuel oils, it was measured at about 246.1 ° C. (475 ° F.).

試験例No.5
本発明による燃料の乳化特性を観察するための安定性試験を行った。実施例1による燃料のバッチをほぼ6日間放置した。実施例1によって調製した燃料バッチを約6日間放置し、それからボイラに着火した。清浄な燃焼が観察され、燃料の分離の兆候もなかった。別のバッチで作った実施例1による追加の燃料22.7リットル(5ガロン)をこの運転中に補助タンクに加えた。追加の燃料が加えられる間に外観上の分離の兆候は認められず、バーナの炎には違いは認められなかった。ボイラの運転は燃料バッチをすべて消費しつくすまで行った。
Test Example No. 5
A stability test was conducted to observe the emulsification characteristics of the fuel according to the present invention. The fuel batch according to Example 1 was left for approximately 6 days. The fuel batch prepared according to Example 1 was left for about 6 days and then the boiler was ignited. Clean combustion was observed and there was no sign of fuel separation. An additional 22.7 liters (5 gallons) of Example 1 made in a separate batch was added to the auxiliary tank during this run. During the addition of additional fuel, there were no signs of visual separation and no difference in the burner flame. The boiler was operated until all fuel batches were consumed.

試験例No.6
ボイラを最適効率付近で運転することによってさらなる排気の試験を行った。試験はNo.5の燃料油バッチで開始し、次いで燃料/空気比の調整はいっさい行わずに実施例1に従って調製した燃料に切り替えた。Enerac2000分析計を用いて窒素酸化物、硫黄酸化物の排出量を測定し、燃焼効率を計算した。結果を下記表1に示す。
Test Example No. 6
Further exhaust tests were performed by operating the boiler near optimal efficiency. The test was No. Starting with 5 fuel oil batches, the fuel / air ratio was then adjusted and switched to the fuel prepared according to Example 1. The emissions of nitrogen oxides and sulfur oxides were measured using an Enerac 2000 analyzer, and the combustion efficiency was calculated. The results are shown in Table 1 below.

Figure 2005530862
Figure 2005530862

試験例No.7
両方の燃料により所定量の蒸気を発生するために消費される燃料の量を決定する比較試験を行った。いずれの試験も水供給ポンプが停止すると同時に燃料バルブを開けて、直ちに開始した。開始時刻を記録し、また水供給の読みも記録した。いずれの試験も燃料23.9リットル(5.264ガロン)を用いて行った。各サンプルはあらかじめ秤量しておいた。いずれの試験も燃料バルブの閉止と、その後の水供給停止時刻の記録によって終了した。水供給ポンプは、所定の低水位でポンプを稼働し、所定の高水位でポンプを停止するMacDonnel Miller No.157装置により自動的に調節した。試験結果を下記表2に示す。
Test Example No. 7
A comparative test was performed to determine the amount of fuel consumed to generate a predetermined amount of steam with both fuels. Both tests were started immediately with the fuel valve open as soon as the water supply pump stopped. The start time was recorded and the water supply reading was also recorded. All tests were conducted using 23.9 liters (5.264 gallons) of fuel. Each sample was weighed in advance. Both tests were completed by closing the fuel valve and recording the subsequent water supply stop time. The water supply pump operates at a predetermined low water level and stops at a predetermined high water level. MacDonnell Miller No. Automatically adjusted by 157 instrument. The test results are shown in Table 2 below.

Figure 2005530862
Figure 2005530862

前記組成物をNo.5のブレンド燃料油の替わりにディーゼル油と混合すること以外は、実施例1と同様にして本発明による燃料を調製した。内燃機関であるRICARD P6ディーゼル燃料試験エンジンによる一連のベンチ試験を本発明の燃料を用いて実施した。ディーゼル燃料対照サンプルを用いて同様のベンチ試験を行った。対照サンプルの試験と本発明の燃料による試験との結果を表3および表4に示す。   The composition was No. A fuel according to the present invention was prepared in the same manner as in Example 1 except that it was mixed with diesel oil instead of the blended fuel oil of No. 5. A series of bench tests with the RICARD P6 diesel fuel test engine, an internal combustion engine, was conducted using the fuel of the present invention. A similar bench test was performed using a diesel fuel control sample. The results of the control sample test and the fuel test of the present invention are shown in Tables 3 and 4.

Figure 2005530862
Figure 2005530862

Figure 2005530862
Figure 2005530862

この結果はすべての回転速度範囲において対照燃料と比較して本発明の燃料の方が燃料消費速度が同等または若干少ないにもかかわらず出力は増大していることを示している。排気温度も表3に比べて表4の方が低いことを示している。未燃焼の析出物も少なくとも本発明の燃料で運転した方が削減される傾向にある。   This result shows that the output of the fuel of the present invention is increased despite the fuel consumption rate being equal or slightly lower than the control fuel in all rotational speed ranges. The exhaust temperature is also lower in Table 4 than in Table 3. Unburned deposits also tend to be reduced when operated with at least the fuel of the present invention.

本発明は内燃機関、開放炎バーナ(ボイラ類)などに用いる、燃料と水の混合物を乳化させるための組成物として実質的な有用性を見出していることを理解されたい。しかし、本発明はこの用途に限定されるものではなく、例えば、タールの付着した道路、コンクリート、石造建築物などの表面から油状付着物をはがす洗浄剤等の他の用途にも使用することができる。   It should be understood that the present invention has found substantial utility as a composition for emulsifying a mixture of fuel and water for use in internal combustion engines, open flame burners (boilers) and the like. However, the present invention is not limited to this application. For example, the present invention may be used for other applications such as a cleaning agent that removes oily deposits from surfaces such as tar-attached roads, concrete, and stone buildings. it can.

Claims (17)

エトキシル化アルキルフェノール;
脂肪酸アミド;
ナフサ;および
オレイン酸
を含有する乳化性組成物。
Ethoxylated alkylphenols;
Fatty acid amides;
An emulsifiable composition containing naphtha; and oleic acid.
前記エトキシル化アルキルフェノールが、ポリオキシエチレン(POE)ノニルフェノールである、請求項1に記載の組成物。   The composition of claim 1, wherein the ethoxylated alkylphenol is polyoxyethylene (POE) nonylphenol. 前記脂肪酸アミドが、脂肪酸ジアルカノールアミドである、請求項1または2に記載の組成物。   The composition according to claim 1 or 2, wherein the fatty acid amide is a fatty acid dialkanolamide. 前記脂肪酸ジアルカノールアミドが、ココナッツジエタノールアミドである、請求項3に記載の組成物。   4. The composition of claim 3, wherein the fatty acid dialkanolamide is coconut diethanolamide. 前記ナフサが、ヘビーナフサである、請求項1から4のいずれか1つに記載の組成物。   The composition according to any one of claims 1 to 4, wherein the naphtha is heavy naphtha. 前記エトキシル化アルキルフェノールがポリオキシエチレンノニルフェノールであり、前記脂肪酸アミドがココナッツジエタノールアミドであり、そして、前記ナフサがヘビーナフサであって、組成物が体積でポリオキシエチレンノニルフェノール1部、ココナッツジエタノールアミド2部、ヘビーナフサ2部、および、オレイン酸1部を含有する、請求項1に記載の組成物。   The ethoxylated alkylphenol is polyoxyethylene nonylphenol, the fatty acid amide is coconut diethanolamide, and the naphtha is heavy naphtha, the composition being 1 part polyoxyethylene nonylphenol, 2 parts coconut diethanolamide, The composition of claim 1 containing 2 parts heavy naphtha and 1 part oleic acid. 請求項1から6のいずれか1つに記載の組成物を含有する炭化水素燃料。   A hydrocarbon fuel containing the composition according to any one of claims 1 to 6. 40体積%以下の水を含有する、請求項7に記載の炭化水素燃料。   The hydrocarbon fuel according to claim 7, containing 40% by volume or less of water. 25体積%以下の水を含有する、請求項8に記載の炭化水素燃料。   The hydrocarbon fuel according to claim 8, containing 25% by volume or less of water. 前記乳化性組成物を体積で1.5%〜2%含有する請求項7から9のいずれか1つに記載の炭化水素燃料。   The hydrocarbon fuel according to any one of claims 7 to 9, which contains the emulsifiable composition in a volume of 1.5% to 2%. 炭化水素燃料に、エトキシル化アルキルフェノール、脂肪酸アミド、ナフサおよびオレイン酸を添加して混合物を生成し、そして、前記混合物に水を添加することを含む、炭化水素燃料と水との乳化物を生成する方法。   Adding an ethoxylated alkylphenol, fatty acid amide, naphtha and oleic acid to a hydrocarbon fuel to produce a mixture, and producing an emulsion of the hydrocarbon fuel and water comprising adding water to the mixture Method. 前記エトキシル化アルキルフェノール、前記脂肪酸アミド、前記オレイン酸および前記ナフサを含有する添加剤組成物を生成し、そして、前記炭化水素燃料に前記添加剤組成物を添加することを含む、請求項11に記載の方法。   12. The method of claim 11, comprising generating an additive composition containing the ethoxylated alkylphenol, the fatty acid amide, the oleic acid, and the naphtha and adding the additive composition to the hydrocarbon fuel. the method of. 前記添加剤組成物が、体積でポリオキシエチレンノニルフェノール1部、ココナッツジエタノールアミド2部、オレイン酸1部、および体積でヘビーナフサ2部を含有する、請求項12に記載の方法。   13. The method of claim 12, wherein the additive composition comprises 1 part polyoxyethylene nonylphenol, 2 parts coconut diethanolamide, 1 part oleic acid, and 2 parts heavy naphtha by volume. 各成分をポリオキシエチレンノニルフェノール、ココナッツジエタノールアミド、オレイン酸およびナフサの順に混合して、前記添加剤混合物を生成する、請求項12または13に記載の方法。   14. The method of claim 12 or 13, wherein each component is mixed in the order of polyoxyethylene nonylphenol, coconut diethanolamide, oleic acid and naphtha to produce the additive mixture. 本明細書に記載されたものと実質的に同一の、請求項1に記載の組成物。   The composition of claim 1, substantially the same as described herein. 本明細書に記載されたものと実質的に同一の、請求項7に記載の炭化水素燃料。   8. A hydrocarbon fuel according to claim 7, substantially the same as described herein. 本明細書に記載されたものと実質的に同一の、請求項11に記載の炭化水素燃料と水との乳化物の生成方法。   12. A method of producing an emulsion of a hydrocarbon fuel and water according to claim 11 substantially the same as described herein.
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CN1297636C (en) 2007-01-31
WO2003075954A1 (en) 2003-09-18
AU2003208499A1 (en) 2003-09-22
CA2518586A1 (en) 2003-09-18
US20050223628A1 (en) 2005-10-13
CN1652818A (en) 2005-08-10

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