[go: up one dir, main page]

TW201219555A - promoting the Brownian motion by the addition of a sublimatable organic compound - Google Patents

promoting the Brownian motion by the addition of a sublimatable organic compound Download PDF

Info

Publication number
TW201219555A
TW201219555A TW099138652A TW99138652A TW201219555A TW 201219555 A TW201219555 A TW 201219555A TW 099138652 A TW099138652 A TW 099138652A TW 99138652 A TW99138652 A TW 99138652A TW 201219555 A TW201219555 A TW 201219555A
Authority
TW
Taiwan
Prior art keywords
hydroxy
isobutyl
methyl
isopropyl
organic compound
Prior art date
Application number
TW099138652A
Other languages
Chinese (zh)
Inventor
kai-xiong Cai
Jian-Li Li
Original Assignee
kai-xiong Cai
Jian-Li Li
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 kai-xiong Cai, Jian-Li Li filed Critical kai-xiong Cai
Priority to TW099138652A priority Critical patent/TW201219555A/en
Priority to US13/200,274 priority patent/US20120110900A1/en
Publication of TW201219555A publication Critical patent/TW201219555A/en

Links

Classifications

    • 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
    • C10L1/1608Well defined compounds, e.g. hexane, benzene
    • 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
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/1822Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
    • C10L1/1824Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
    • 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
    • C10L1/185Ethers; Acetals; Ketals; Aldehydes; Ketones
    • C10L1/1852Ethers; Acetals; Ketals; Orthoesters
    • C10L1/1855Cyclic ethers, e.g. epoxides, lactides, lactones
    • 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
    • C10L1/185Ethers; Acetals; Ketals; Aldehydes; Ketones
    • C10L1/1857Aldehydes; Ketones
    • 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
    • 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
    • C10L2230/00Function and purpose of a components of a fuel or the composition as a whole
    • C10L2230/22Function and purpose of a components of a fuel or the composition as a whole for improving fuel economy or fuel efficiency

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Combustion & Propulsion (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The present invention provides an additive for increasing the combustion efficiency of a liquid fuel, comprising sublimatable organic compound and a liquid fuel, wherein the sublimatable organic compound is in a solid state at atmospheric pressure and below 45 DEG C. The sublimatable organic compound added in the present invention enhances diffusion of the Brownian motion to allow the liquid fuel to be more uniformly heated and increase the combustion efficiency of the liquid fuel. The present invention also provides a method for increasing combustion efficiency of liquid fuel achieved by adding the sublimatable organic compound into a liquid fuel.

Description

201219555 六、發明說明: 【發明所屬之技術領域】 本發明是有關於一種提昇揪植 ^ 汁燃燒效率的添加劑及方法 特別是指一種提昇液態燃料姆燒 邝…現政率的添加劑及方法。 【先前技術】 k著全球能源危機及環境污染等問題日益嚴重, 的解決方案除了尋求替代能 外’更急需尋求提昇 的燃燒效率並降低燃料用詈的古201219555 VI. Description of the Invention: [Technical Field of the Invention] The present invention relates to an additive and method for improving the combustion efficiency of a simmering juice, in particular, an additive and method for increasing the current rate of liquid fuel smoldering. [Prior Art] K. The global energy crisis and environmental pollution are becoming more and more serious. In addition to seeking alternative energy, the solution is more urgent to seek improved combustion efficiency and reduce the use of fuel.

、 利里的方法。現有提昇燃燒效率的 方法相當多樣化,除了從故p 良九,' 裝置的機械結構著手 外,各式燃料添加劑的傕用> sV t 便用也疋各界所知悉的方法。例如 在無鉛汽油中添加4〜1〇 wt%甲基第三丁基醚(Me_ teniary b卿i ether,MEBT),可幫助汽油完全燃燒並減少 :氧化碳的排放量。但甲基第三丁基醚會引起中樞神經中 ,,長期吸入或暴露於存有甲基第三丁基醚的環境下,恐 引起器官病變以及癌症。 中華民國專利公開案第200927912號揭示一種車輛、 軋舶專用的環保省油精。將此種含有能源活化劑及2_甲基-2_丙醇的液態省油精加入油箱内與燃料均勻混合,可以改善 燃料燃燒不完全的情況。此專利所使用的2_甲基_2_丙醇之 毒性及麻醉性較一般醇類高,故此一環保省油精在使用上 仍有傷害人體及環境的疑慮。 中華民國專利公開案第200825163號提供一種利用分. 子震盡原理的省油粉末,此省油粉末具有遠紅外線及負離 子效能,經由奈米技術處理且由氧化鋅、二氧化矽、碳酸 201219555 妈、氧化鎂、氧化鉀、氧化鋁、稀土元素及微量元素所組 成。此種省油粉末由多種固態無機物所組成,且須經過奈 米技術處理,除了製程上較為繁雜之外,更可能產生與燃 料之間不相容、自身團聚所造成的分散不均勻等問題。 其他燃料添加劑還包括金屬氧化物、過渡金屬氧化物 及雙環芳香族化合物,其中,金屬氧化物(如氧化辞、氧化 鎮)作為非勻相催化劑’雙環芳香族化合物作為還原劑。藉 由雙環芳香族化合物還原過渡金屬氧化物來活化金屬氧化 物進而提昇燃料的燃燒效率。但此添加劑中所使用的金 屬氧化物,除成本較高外,亦為毒性物質,長期使用會對 人體及環*兄造成負擔。另一種添加劑為可完全溶解於燃料 中的有機化合物(如笨曱酸),此種添加劑使燃料的密度及黏 度降低,幫助混合燃料中各種難溶組份,使燃料燃燒更完 由上述可知’目前的燃料添加劑除製程較複雜外,仍 有對%境及使用者造成危害之疑慮,因此,尋求僅需少量 添加且無毒無污染的燃料添加劑,實為迫切所需的❶ 【發明内容】 為了改善習知燃料添加劑之組份及製程繁雜、損害環 境及人體健康等問冑’本案發明人首先思及將昇華的概念 應用在燃料添加劑上,在多方試驗後,尋得—種無毒、= 乳味且僅需少量添加便可提昇液態燃料之燃燒效率的添加 劑。 因此,本發明之目的,即在提供一種用於提昇液態燃 201219555 料燃燒效率的添加劑,包人· 態燃料,其中,# 3 胃可昇華有機 下為固態。 一可昇華有機化合物及一液 化合物在一大氣壓及45°C以 本發明之另一 ^一目的在於提供一種用於提昇液態燃料燃 k政率的方法,县 _ ,, 疋透過將—可昇華有機化合物加入一液態 燃料中而完成,复中 ‘ /、中該可汁華有機化合物在一大氣壓及 45C以下為固態。, Lili's method. The existing methods for improving combustion efficiency are quite diverse, and in addition to the mechanical structure of the device, the use of various fuel additives is also known to the public. For example, adding 4~1〇 wt% methyl tert-butyl ether (MET) to unleaded gasoline can help complete combustion of gasoline and reduce carbon oxide emissions. However, methyl tert-butyl ether causes central nervous system damage, which may cause organ damage and cancer in long-term inhalation or exposure to methyl tert-butyl ether. The Republic of China Patent Publication No. 200927912 discloses an environmentally-friendly and fuel-efficient oil for vehicles and rolling boats. The liquid fuel-saving concentrate containing the energy activator and 2-methyl-2-propanol is uniformly mixed with the fuel in the fuel tank, which can improve the incomplete combustion of the fuel. The toxicity and anesthetic properties of 2-methyl-2-propanol used in this patent are higher than those of common alcohols. Therefore, the environmentally-friendly and oil-efficient oils still have doubts about the human body and the environment. The Republic of China Patent Publication No. 200825163 provides an energy-saving powder utilizing the principle of sub-shocking, which has far-infrared and negative ion efficiencies, is treated by nanotechnology and is oxidized by zinc oxide, cerium oxide, carbonic acid 201219555 It consists of magnesium, potassium oxide, aluminum oxide, rare earth elements and trace elements. This kind of fuel-saving powder is composed of a variety of solid inorganic materials and must be treated by nanotechnology. In addition to the complicated process, it is more likely to cause problems such as incompatibility with fuel and uneven dispersion caused by self-aggregation. Other fuel additives also include metal oxides, transition metal oxides, and bicyclic aromatic compounds in which metal oxides (e.g., oxidized, oxidized) are used as the non-homogeneous catalyst 'bicyclic aromatic compounds as reducing agents. The transition metal oxide is reduced by a bicyclic aromatic compound to activate the metal oxide to improve the combustion efficiency of the fuel. However, the metal oxide used in this additive is also a toxic substance in addition to the higher cost, and the long-term use imposes a burden on the human body and the ring. Another additive is an organic compound (such as scorpion acid) that is completely soluble in the fuel. This additive reduces the density and viscosity of the fuel, helps the various insoluble components in the fuel mixture, and makes the fuel burn more. In addition to the complicated process, the current fuel additives still have doubts about the harm to the environment and users. Therefore, it is urgent to find a fuel additive that requires only a small amount of addition and is non-toxic and non-polluting. [Inventive content] Improvement of the composition and process of conventional fuel additives, damage to the environment and human health. The inventor of this case first thought of applying the concept of sublimation to fuel additives. After multiple tests, it was found to be non-toxic, = milk. An additive that enhances the combustion efficiency of liquid fuels with a small addition. Accordingly, it is an object of the present invention to provide an additive for enhancing the combustion efficiency of a liquid fuel 201219555, which comprises a human fuel, wherein #3 can be sublimed organically in a solid state. A sublimable organic compound and a liquid compound at atmospheric pressure and 45 ° C. Another object of the present invention is to provide a method for increasing the fuel economy of a liquid fuel, and the county can be sublimated. The organic compound is added to a liquid fuel, and the organic compound in the middle of the complex is at a pressure of at most atmospheric pressure and below 45C.

中==明藉由添加一可昇華有機化合物至一液態燃料 :衣蜓/孤度上升時,該可昇華有機化合物將由固態昇 華:氣態’再由液態燃料釋出時,將於液態燃料中形成一 擾流:加強擴散型布朗運動,使得該液態燃料會因擾流而 句勻又熱且更易於轉化為小分子或氣態分子;&,透過該 可昇華有機化合物昇華轉變為氣態化合物,更可協助轉變 為小分子或氣態分子的液態燃料擴散並均勻地燃燒進而 提昇液態燃料的燃燒效率。本發明添加劑所含的可昇華有 機化合物具備無毒、低氣味且添加量少等優點,完全不會 造成環境及人體的傷害。 【實施方式】 本發明之一種用於提昇液態燃料燃燒效率的添加劑, 包含一可昇華有機化合物及一液態燃料,其中,該可昇華 有機化合物在一大氣壓及45°C以下為固態。 較佳地’該可昇華有機化合物含有一骨架,該骨架a 選自於雙環庚烷(bicyclic heptane)、萘(naphthalene)、二 τ ·*Λ* 茚(indan)、。比喃酮(pyrone)、環丙烷、環丁烷、環戊燒、淨 5 201219555 己烷、環庚烷、環辛烷或苯。 以下將依據上述所列舉之骨架,說明可昇華有機化合 物的例子: 1. 含有雙環庚烷骨架的可昇華有機化合物可包含,但不 限於:天然材料:如樟腦、茨醇(bornyl alcohol)、茨稀 (camphene)等。合成材料:例如:Medium == Ming by adding a sublimable organic compound to a liquid fuel: when the clothing/orphanity rises, the sublimable organic compound will be sublimated by the solid state: when the gaseous state is released from the liquid fuel, it will form in the liquid fuel. A turbulent flow: enhanced diffusion Brownian motion, which makes the liquid fuel uniform and hot due to turbulence and more easily converted into small molecules or gaseous molecules; &, through the sublimation of organic compounds, sublimation into gaseous compounds, The liquid fuel that can be converted into small molecules or gaseous molecules can be diffused and uniformly burned to improve the combustion efficiency of the liquid fuel. The sublimable organic compound contained in the additive of the present invention has the advantages of being non-toxic, low in odor, and having a small amount of addition, and does not cause environmental or human damage at all. [Embodiment] An additive for improving the combustion efficiency of a liquid fuel of the present invention comprises a sublimable organic compound and a liquid fuel, wherein the sublimable organic compound is solid at atmospheric pressure and below 45 °C. Preferably, the sublimable organic compound contains a skeleton selected from bicyclic heptane, naphthalene, and in?. Pyrone, cyclopropane, cyclobutane, cyclopentane, net 5 201219555 hexane, cycloheptane, cyclooctane or benzene. Examples of sublimable organic compounds will be described below based on the skeletons listed above: 1. Sublimable organic compounds containing a bicycloheptane skeleton may include, but are not limited to, natural materials such as camphor, bornyl alcohol, and Lean (camphene) and so on. Synthetic materials: for example:

[2-羥基-2,6,6-三曱基雙環[3.1.1]-2-庚烷] 其合成方法如下: ch3v^ch3[2-Hydroxy-2,6,6-trimethylbicyclo[3.1.1]-2-heptane] The synthesis method is as follows: ch3v^ch3

CH3 2HBr reflux _ H3C (THF) ch3v.ch3CH3 2HBr reflux _ H3C (THF) ch3v.ch3

3 NaOH3 NaOH

如下: [4,7,7-三甲基雙環[2.2.1]庚酮],其合成方法 201219555As follows: [4,7,7-trimethylbicyclo[2.2.1]heptanone], its synthesis method 201219555

Cl + 2 NaOH —► 〇H ΟCl + 2 NaOH —► 〇H Ο

Cl + 2 HC1Cl + 2 HC1

H3C^/CH3H3C^/CH3

,^^0H, ^^0H

[4,7,7-三甲基雙環[2.2.1]庚醇],其合成方法 如下:[4,7,7-trimethylbicyclo[2.2.1]heptanol], the synthesis method is as follows:

2. 含有萘骨架的可昇華有機化合物可包含但不限於:天 然材料如萘、β-萘甲醚(β-naphthol methylether)、β-萘 乙醚(β-naphtholethylether)等。 201219555 3. 含有二氫茚骨架的可昇華有機化合物可包含但不限 於:天然材料如5-乙醯基-1,1,2,3,3,6-六甲基二氫茚(5-acetyl-l,l,2,3,3,6-hexamethyl indan,phantolide)、4-乙 酿基-6-第三丁基-1,1_ 二甲基二氫茚(4-306{)^1-6461>1:-butyl-l,l-dimethylindan,celestolide)、1,1,4,4-四曱基-6-乙基-7-乙酿基-1,2,.3,4-四氫萘(1,1,4,4七的11^1171-6-ethyl-7-acetyl-l,2,3,4-tetrahydronaphthalene 5 versalide) 等。 4.含有°比喃酮骨架的可昇華有機化合物可包含但不限 於·天然材料如麥芽酚(malt〇l , 3-羥基_2_甲基_γ_吡喃 酮)。 5·含有環丙烷骨架的可昇華有機化合物可包含但不限 於:合成材料如: CH,2. The sublimable organic compound containing a naphthalene skeleton may include, but is not limited to, natural materials such as naphthalene, β-naphthol methylether, β-naphtholethylether, and the like. 201219555 3. Sublimable organic compounds containing an indoline skeleton may include, but are not limited to, natural materials such as 5-ethenyl-1,1,2,3,3,6-hexamethylindoline (5-acetyl) -l,l,2,3,3,6-hexamethyl indan,phantolide), 4-ethyl-branched-6-t-butyl-1,1-dimethyl indoline (4-306{)^1- 6461>1:-butyl-l,l-dimethylindan,celestolide), 1,1,4,4-tetradecyl-6-ethyl-7-ethenyl-1,2,.3,4-tetrahydrogen Naphthalene (11^1171-6-ethyl-7-acetyl-l, 2,3,4-tetrahydronaphthalene 5 versalide) of 1,1,4,4,7, and the like. 4. The sublimable organic compound containing a pyrone skeleton may include, but is not limited to, a natural material such as malt phenol (malt〇l, 3-hydroxy-2-methyl_γ-pyranone). 5. The sublimable organic compound containing a cyclopropane skeleton may include, but is not limited to, a synthetic material such as: CH,

[2-異丁基-3-異丙基環丙醇]、[2-isobutyl-3-isopropylcyclopropanol],

[2-異丁基·3_異丙基環丙酮]等。 3有環丁烷骨架的可昇華有機化合物 於·合成材料如: 可包含但不限 201219555[2-Isobutyl-3_isopropylcyclopropanone] and the like. 3 Sublimable organic compounds with a cyclobutane skeleton. Synthetic materials such as: May be included but not limited 201219555

ch3 [2-異丁基-4-乙基環丁醇]Ch3 [2-isobutyl-4-ethylcyclobutanol]

CH3 [2-異丁基-4-乙基環丁酮]等 7. 含有環戊烷骨架的可昇華有機化合物可包含但不限 於:合成材料如:CH3 [2-isobutyl-4-ethylcyclobutanone], etc. 7. The sublimable organic compound containing a cyclopentane skeleton may include, but is not limited to, a synthetic material such as:

ch3 h3c--ch3 [2-異丁基-4-曱基環戊醇]Ch3 h3c--ch3 [2-isobutyl-4-mercaptocyclopentanol]

h3c [2-異丁基-4-曱基環戊酮]等。 8. 含有環己烷骨架的可昇華有機化合物可包含但不限 於:天然材料如薄荷醇(menthol)、第三丁基環己醇 (tert-butylcyclohexanol)等。合成材料例如: 201219555H3c [2-isobutyl-4-mercaptocyclopentanone] and the like. 8. The sublimable organic compound containing a cyclohexane skeleton may include, but is not limited to, natural materials such as menthol, tert-butylcyclohexanol, and the like. Synthetic materials such as: 201219555

荷酮(menthol)],其合成方法如下:The ketone (menthol)], the synthesis method is as follows:

+ NaOH+ NaOH

衍 生自苧烯(limonene)],其合成方法如下: H3C、/Br ch3Derived from limonene], the synthesis method is as follows: H3C, /Br ch3

+ Br2 Δ reflux (THF) h3c-+ Br2 Δ reflux (THF) h3c-

Br CH,Br CH,

+ NaOH+ NaOH

H3C ^ch2H3C ^ch2

酮,衍生自香芹酮(carvone)],其合成方法如下: 10 201219555Ketone, derived from carvone, is synthesized as follows: 10 201219555

_(piperitone)],其合成方法如下:_ (piperitone)], its synthesis method is as follows:

H3C\/〇HH3C\/〇H

+ NaOH+ NaOH

h3c CH3 [5-羥基-5·曱基_2-(l-曱基亞乙基)環己烷,衍生自 胡薄荷顚I (pulegone)],其合成方法如下:H3c CH3 [5-Hydroxy-5.indolyl-2-(l-decylethylene)cyclohexane, derived from pulegone], is synthesized as follows:

++

+ NaOH+ NaOH

HSC CH3 [2_(4_羥基_4_曱基環己烷基)異丙醇,衍生自α_ 11 201219555 萜品醇(terpineol)],其合成方法如下 CH, H3C\/BrHSC CH3 [2_(4_hydroxy_4_decylcyclohexane)isopropanol, derived from α_ 11 201219555 terpineol], synthesized as follows CH, H3C\/Br

H3C. .OH Δ HBrH3C. .OH Δ HBr

OH reflux (THF) 火、 h3c/vch3OH reflux (THF) fire, h3c/vch3

+ NaOH+ NaOH

.OH j^OH h3c/^ch3.OH j^OH h3c/^ch3

H3C. .OH H3C 013 [1-羥基-1-曱基-4-(1-曱基亞乙基)環己烷,衍生自 萜品油烯(terpinolene)],其合成方法如下:H3C. .OH H3C 013 [1-hydroxy-1-indolyl-4-(1-mercaptoethylidene)cyclohexane, derived from terpinolene], is synthesized as follows:

+ NaOH+ NaOH

[1-羥基-2-異丁基環己烷],其合成方法如下:[1-Hydroxy-2-isobutylcyclohexane], which is synthesized as follows:

Cl Cl OHCl Cl OH

Cl2 ——► + HC1 + NaOHCl2 ——► + HC1 + NaOH

OH H2S04 CH3 ci士 CH3 CH, CH, "CH3 + Bf2 CH,OH H2S04 CH3 ci 士 CH3 CH, CH, "CH3 + Bf2 CH,

BrBr

OH CH, CH, -CH:OH CH, CH, -CH:

+ NaOH -CH3 CH, CH, 12 201219555+ NaOH -CH3 CH, CH, 12 201219555

[1-羥基-1-異丁基環己烷] 其合成方法如下:[1-Hydroxy-1-isobutylcyclohexane] The synthesis method is as follows:

OH CH, >~/ CH, H3C· -CH, CH3 /~ CH3 H0 [1,4-二羥基-3,6-二異丁基環己烷],其 合成方法如下: 2C1, -^ C1 〇OH CH, >~/ CH, H3C·-CH, CH3 /~ CH3 H0 [1,4-dihydroxy-3,6-diisobutylcyclohexane], the synthesis method is as follows: 2C1, -^ C1 〇

Cl + 2 HC1Cl + 2 HC1

Cl +2NaOH-►OH o + 2 严 A1C13 d〇i3 ^ H3C_ ch3 CH, ,__Λ CH, -CH, + Br,Cl +2NaOH-►OH o + 2 严 A1C13 d〇i3 ^ H3C_ ch3 CH, ,__Λ CH, -CH, + Br,

BrBr

OH CH, ,一_l CH, -CH, CH, _CH3 + 2NaOH—► H3C- ch3OH CH, , a _l CH, -CH, CH, _CH3 + 2NaOH—► H3C- ch3

HOHO

[1-羥基-3,6-二異丁基環己烷],其合成方法如 13 201219555 下:[1-Hydroxy-3,6-diisobutylcyclohexane], the synthesis method is as follows: 13 201219555

CH3 ——CH3 ch3CH3 ——CH3 ch3

HOHO

其合成方法如 [1-羥基-4-異丁基環己烷]Its synthesis method is [1-hydroxy-4-isobutylcyclohexane]

ch3 ——ch3 ch3Ch3 ——ch3 ch3

[2-異丁基環己酮],其合成方法如下: 14 201219555[2-Isobutylcyclohexanone], the synthesis method is as follows: 14 201219555

OHOH

CH3 [1-羥基-3-異丙基-6-曱基環己烷],其合成 方法如下:CH3 [1-hydroxy-3-isopropyl-6-fluorenylcyclohexane], which is synthesized as follows:

ch3 h3c--ch3Ch3 h3c--ch3

OHOH

[2-異丁基環己醇]、 15 201219555[2-isobutylcyclohexanol], 15 201219555

H3CH3C

[2_異丁基環己酮]等。 9.含有環庚院骨架的可昇基古換&人d J J什華有機化合物可包含但不 於:合成材料如: CH3\ /(¾ 限[2_Isobutylcyclohexanone] and the like. 9. Can be used in the ring-gathering framework. The human d J J Shihua organic compound may contain but not: synthetic materials such as: CH3\ / (3⁄4 limit

OHOH

[4-異丙基環庚醇]、[4-isopropylcycloheptanol],

CH3\ CHCH3\ CH

〇 [4-異丙基環庚酮]等。 含有環辛院骨架的可昇華有機化合物可包含但 於:合成材料如: 不限〇 [4-isopropylcycloheptanone] and the like. The sublimable organic compound containing the ring of the Xinxinyuan skeleton may include: synthetic materials such as:

不限於:合 11.含有苯骨架的可昇華有機化合物可包含但 成材料如: 16 201219555 [1-甲基-2,5-二異丁基_4_異丙基苯]等。It is not limited to: 11. The sublimable organic compound containing a benzene skeleton may be contained as a material such as: 16 201219555 [1-methyl-2,5-diisobutyl-4-isopropylbenzene].

^ >更佳地,該可昇華有機化合物是選自於樟腦、萘、薄 荷醇、茨醇、茇烯、第三丁基環己醇、麥芽酚、5-乙醯基· 1’1’2,3,3,6-六曱基二氫茚、4_乙醯基_6第三丁基Μ·二甲基 一虱印、1,1,4,4-四甲基_6·乙基_7•乙醢基义^心四氫蔡、 β_萘甲醚、β-蔡乙醚、2·異丙基_2,5_二羥基_5_甲基環己酮、 1-曱基-1-經基-4-(1_甲基·基乙基)環己烧、2_甲基_3•經 基-5-羥基-5-(1-甲基乙烯基)_2•環己酮' 弘曱基_3•羥基_6_異 丙基-環己嗣、5_經基_5_甲基_2_(1_甲基亞乙基)環己烷、2_ 羥基^-三甲基雙環^丄叫-庚院…心經基冰甲基小 環己烧基)異丙醇、卜經基]_甲基冬(1_甲基亞乙基)環己 烷、1-甲基-2,5-二異丁基_4_異丙基苯、卜經基-2_異丁基環 己烷、1·羥基_1_異丁基環己烷、M_二羥基·3,6_二異丁基環 己烷、1-經基-3,6-二異丁基環己烷、卜經基_心異丁基環己 烷、4,7,7-三甲基雙環[2.2]]庚酮、4,7,7_三甲基雙環[221] 庚醇、1-經基-3-異丙基_6·甲基環己烷、2_異丁基_3_異丙基 琢丙酮、2-異丁基_3_異丙基環丙醇、2_異丁基乙基環丁 酮、2-異丁基_4_乙基環丁醇、2_異丁基_4·甲基環戍酮、^ 異丁基-4-甲基裱戊醇、2_異丁基環己酮、2_異丁基環己醇、 4-異丙基%庚酮、4-異丙基環庚醇、3,7_二曱基環辛酮' 3,7-二甲基環辛酮’或上述可昇華有機化合物的—組合。又 更佳地,該可昇華有機化合物是選自於薄荷醇、茨醇、茨 17 201219555 烯、第三丁基環己醇、麥芽酚、5_乙醯基·丨山^ 6_六甲 基二氫節、4-乙醯基-6-第三丁基」,丨_二甲基二氫茚、 1,1,4,4-四曱基-6-乙基-7-乙醯基·1,2,3,4_四氫萘、β-萘甲 醚、β-萘乙醚、2-異丙基_2,5-二羥基-5-曱基環己酮、1-甲 基-1-羥基-4-(1-曱基-1-羥基乙基)環己烷、2_曱基_3_羥基_5_ 羥基-5-(1-甲基乙烯基)-2-環己酮、3_曱基_3_羥基_6_異丙基_ 環己酮、5-羥基-5-曱基·2·(1-曱基亞乙基)環己烷、2-羥基- 2.6.6- 三甲基雙環[3_1.1]-2-庚烷、2-(4-羥基-4-曱基-1-環己 烷基)異丙醇、1-羥基-1-曱基·4·(!_曱基亞乙基)環己烷、卜 甲基-2,5-二異丁基-4-異丙基苯、丨_羥基_2_異丁基環己烷、 1-羥基-1-異丁基環己烷、1,4_二羥基_3,6_二異丁基環己烷、 1-羥基-3,6-二異丁基環己烷、丨_羥基_4_異丁基環己烷、 4.7.7- 三曱基雙環[2.2· 1]庚酮、4,7,7-三曱基雙環[2.2.1]庚 醇、1-羥基-3-異丙基-6-甲基環己烷、2_異丁基_3_異丙基環 丙酮、2-異丁基-3-異丙基環丙醇、2_異丁基·4_乙基環丁 酮、2-異丁基-4-乙基環丁醇、2-異丁基曱基環戊酮、2-異丁基-4-曱基環戊醇、2-異丁基環己酮、2-異丁基環己醇、 4-異丙基環庚酮、4-異丙基環庚醇、3,7_二曱基環辛酮、 3.7- 二甲基環辛酮,或上述可昇華有機化合物的一組合。 上述之可昇華有機化合物為天然的成分或其衍生物, 部分帶有淡淡香氣,不會對環境造成負擔。 較佳地,每10公升的液態燃料添加〇 5〜5〇()公克的可 昇華有機化合物。 較佳地’該液態燃料是選自於汽油、柴油、酒精、生 18 201219555 質汽油、生質柴油、生質酒精、 負⑯有機氫化燃料油或上述燃 料之一組合。其中有機氫化燃料 了寸,由可例如但不限於環己 烧、甲基環己烷及十氫化萘。 θ發明之用於提昇液態燃料燃燒效率的方法是透過將一 可幵華有機化合物加人-液態燃料中而完成,《中,該可 昇華有機化合物與該液態燃料之態樣及變化是如上所=, 在此不多加費述。 本發明將就以下實施例來作進一步說明,但應瞭㈣ 是’該實施例僅為例示說明之用,而不應被解釋為本發明 實施之限制。^> More preferably, the sublimable organic compound is selected from the group consisting of camphor, naphthalene, menthol, benzyl alcohol, decene, t-butylcyclohexanol, maltol, 5-ethylindenyl 1'1 '2,3,3,6-hexamethylenedihydroindole, 4_acetamido_6 tert-butyl fluorene dimethyl oxime, 1,1,4,4-tetramethyl _6· Ethyl_7•Ethyl hydrazine, tetrahydrogen, β-naphthyl ether, β-caethyl ether, 2·isopropyl-2,5-dihydroxy-5-methylcyclohexanone, 1-曱1-yl-1-yl-4-(1-methylethyl)cyclohexanyl, 2-methyl-3-3-trans--5-hydroxy-5-(1-methylvinyl)_2• ring Hexanone 'Hongkung _3•hydroxyl_6_isopropyl-cyclohexanium, 5_carbyl_5_methyl_2_(1_methylethylidene)cyclohexane, 2_hydroxy^-three Methyl double ring ^ 丄 - 庚 庚 庚 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 心 庚 庚 庚 庚 庚 庚 庚 庚 庚 庚,5-diisobutyl-4_isopropylbenzene, bismyl-2-isobutylcyclohexane, 1·hydroxy_1_isobutylcyclohexane, M_dihydroxy·3,6_diiso Butylcyclohexane, 1-carbyl-3,6-diisobutylcyclohexane, dipyridyl-p-isobutylcyclohexane, 4,7,7-trimethylbicyclo[2 .2]]heptanone, 4,7,7-trimethylbicyclo[221]heptanol, 1-perzyl-3-isopropyl-6-methylcyclohexane, 2-isobutyl_3_ Isopropyl acetonone, 2-isobutyl _3_isopropylcyclopropanol, 2-isobutylethylcyclobutanone, 2-isobutyl-4-ethylcyclobutanol, 2-isobutyl _4·methylcyclononanone, ^isobutyl-4-methylamyl alcohol, 2-isobutylcyclohexanone, 2-isobutylcyclohexanol, 4-isopropyl% heptanone, 4-isopropylcycloheptanol, 3,7-didecylcyclooctanone '3,7-dimethylcyclooctanone' or a combination of the above sublimable organic compounds. More preferably, the sublimable organic compound is selected from the group consisting of menthol, benzyl alcohol, Benz 17 201219555 olefin, tert-butylcyclohexanol, maltol, 5-ethylidene·丨山^ 6_hexa Dihydrogen, 4-ethinyl-6-t-butyl", 丨-dimethyl indoline, 1,1,4,4-tetradecyl-6-ethyl-7-ethenyl · 1,2,3,4_tetrahydronaphthalene, β-naphthylmethyl ether, β-naphthyl ether, 2-isopropyl-2,5-dihydroxy-5-fluorenylcyclohexanone, 1-methyl- 1-hydroxy-4-(1-mercapto-1-hydroxyethyl)cyclohexane, 2-hydrazino-3-hydroxy-5-hydroxy-5-(1-methylvinyl)-2-cyclohexanone 3_曱基_3_hydroxy_6_isopropyl_cyclohexanone, 5-hydroxy-5-fluorenyl-2(1-mercaptoethylidene)cyclohexane, 2-hydroxy-2.6. 6-trimethylbicyclo[3_1.1]-2-heptane, 2-(4-hydroxy-4-mercapto-1-cyclohexane)isopropanol, 1-hydroxy-1-indenyl·4 · (!_曱-ethylidene) cyclohexane, methyl-2,5-diisobutyl-4-isopropylbenzene, hydrazine-hydroxy-2-isobutylcyclohexane, 1-hydroxy-1 -isobutylcyclohexane, 1,4-dihydroxy-3,6-diisobutylcyclohexane, 1-hydroxy-3,6-diisobutylcyclohexane, 丨_hydroxy_4_ Butylcyclohexane, 4.7.7-three Bicyclo[2.2.1]heptanone, 4,7,7-trimercaptobicyclo[2.2.1]heptanol, 1-hydroxy-3-isopropyl-6-methylcyclohexane, 2-isobutyl Base_3_isopropylcyclopropanone, 2-isobutyl-3-isopropylcyclopropanol, 2-isobutyl-4-isocyclobutanone, 2-isobutyl-4-ethylcyclo Butanol, 2-isobutyldecylcyclopentanone, 2-isobutyl-4-mercaptocyclopentanol, 2-isobutylcyclohexanone, 2-isobutylcyclohexanol, 4-isopropyl A cyclohexanone, 4-isopropylcycloheptanol, 3,7-didecylcyclooctanone, 3.7-dimethylcyclooctanone, or a combination of the above sublimable organic compounds. The above-mentioned sublimable organic compound is a natural component or a derivative thereof, and partially has a light aroma, and does not burden the environment. Preferably, 5 to 5 Å (grams) of sublimable organic compound is added per 10 liters of liquid fuel. Preferably, the liquid fuel is selected from the group consisting of gasoline, diesel, alcohol, raw gasoline, biodiesel, raw alcohol, negative 16 organic hydrogenated fuel oil, or a combination of the foregoing. Among them, the organic hydrogenated fuel may be, for example, but not limited to, cyclohexene, methylcyclohexane and decalin. The method for increasing the combustion efficiency of a liquid fuel by θ is accomplished by adding a Kelly organic compound to a human-liquid fuel, wherein the sublimation organic compound and the liquid fuel are as described above. =, there is no more to mention here. The invention is further illustrated by the following examples, which are intended to be illustrative only and not to be construed as limiting.

<實施例> [實施例1J 將2.5公克的1_經基_4_異丁基環己烧加入5〇公升的 市售柴油中,製得實施例1之添加劑。 (測試)將實施例1的添加劑加入一柴油車TUCS〇ND_ DX2(排氣量為2000C.C.,馬力為136hp,2〇〇7年 11月出廠)的空油箱中,於一般道路上不定速行 駛,測試該柴油車可行駛之公里數,獲得之公里 數為560公里。(測試地點為大陸深圳) (二白试驗)使用上述測試的同一柴油車,並於其空油箱 中加入50公升的柴油’再測試該柴油車於 一般道路上不定速可行駛之公里數,獲得之 公里數為480公里。 (結果)由上述結果可知,實施例1的添加劑可讓柴油車 19 201219555 【實ι 可行駛之公里數由480公里提昇至560公里。 I頁苑例2】 字2.5公克的2 -異丁基環己酮加入6〇公升的95無錯 ^气ί由 '干’製得實施例2之添加劑。 (測執) ^ 將貫施例2的添加劑加入一汽油車奥迪A8〇(排氣 量為2000C.C. ’馬力為175hp,2002年10月出 廠)的空油箱中’於一般道路上不定速行駛,測試 該汽油車可行駛之公里數’獲得之公里數為43〇 公里。(測試地點為大陸深圳) 試驗)使用上述測試的同一汽油車,並於其空油箱 中加入60公升的95無鉛汽油,再測試該汽 油車於一般道路上不定速可行駛之公里數, 獲得之公里數為350公里。 (結果)由上述結果可知,實施例2的添加劑可讓汽油車 可行駛之公里數由350公里提昇至43〇公里。 [實施例3】 將2.5公克# i,基_3_異丙基_6•甲基環己烷加入% 公升的97無鉛汽油中,製得實施例3之添加劑。 (測試)f實施例3的添加劑加入一汽油車本田雅哥(排氣 量為3000C.C.,馬力為2〇〇hp,2〇〇3年6月出廠) 的空油箱中,於—般道路上不定速行駛’測試該 汽油車可行驶之公里數,獲得之公里數為450公 里。(測試地點為大陸深圳) (空白試驗)使用上述測試的同一汽油車,並於其空油箱 20 201219555 :=5°公升的97無敍汽油’再測試該汽 油車於一般道路上不定速可行歇之公里數, 獲得之公里數為350公里。 (結果)自上述結果可知,實施例3的添加劑可讓汽油車 可行駛之公里數由350公里提昇至45〇公 [實施例4] (測試) —將2.5公克的2•異丁基環己醇加入6〇公升的%無錯 汽油中,製得實施例4之添加劑。 ‘·'、。<Examples> [Example 1J An additive of Example 1 was obtained by adding 2.5 g of 1-_base-based 4-isobutylcyclohexane to 5 liters of commercially available diesel oil. (Test) Add the additive of Example 1 to an empty fuel tank of a diesel vehicle TUCS 〇 ND_ DX2 (with a displacement of 2000 C.C., a horsepower of 136 hp, which was delivered in November 2007). At a fixed speed, test the number of kilometers that the diesel car can travel, and the number of kilometers obtained is 560 kilometers. (The test location is Shenzhen, China) (Two white test) The same diesel vehicle tested above was used, and 50 liters of diesel oil was added to its empty fuel tank. Then test the number of kilometers that the diesel vehicle can travel at a fixed speed on a general road. The number of kilometers obtained is 480 kilometers. (Results) From the above results, it is understood that the additive of the embodiment 1 can make the diesel vehicle 19 201219555 [the number of kilometers that can be traveled from 480 km to 560 km. I Page 2 Example 2] 2.5 g of 2-isobutylcyclohexanone was added to 6 liters of 95 without error. The additive of Example 2 was obtained from 'dry'. (Measurement and Control) ^ Add the additive of Example 2 to a petrol car Audi A8 〇 (displacement of 2000C.C. 'horsepower is 175hp, factory in October 2002) in the empty fuel tank 'on the general road uncertain Speed driving, test the number of kilometers that the gasoline car can travel 'the number of kilometers obtained is 43 kilometers. (Test location is Shenzhen, China) Test) Use the same gasoline vehicle tested above, and add 60 liters of 95 unleaded gasoline to its empty fuel tank, and then test the number of kilometers that the gasoline vehicle can travel at a fixed speed on a general road. The number of kilometers is 350 kilometers. (Results) From the above results, the additive of Example 2 can increase the number of kilometers that a gasoline vehicle can travel from 350 kilometers to 43 kilometers. [Example 3] An additive of Example 3 was obtained by adding 2.5 gram of # i, ki_3_isopropyl_6-methylcyclohexane to a % liter of 97 unleaded gasoline. (Test) f The additive of Example 3 was added to an empty fuel tank of a gasoline vehicle Honda Yage (with a displacement of 3000 C.C., a horsepower of 2 hp, and a delivery of 2 〇〇 3 years). Driving at a fixed speed on the road' test the number of kilometers that the petrol car can travel, and the number of kilometers obtained is 450 kilometers. (Test location is Shenzhen, China) (Blank test) Use the same gasoline vehicle tested above, and in its empty fuel tank 20 201219555: = 5 ° liter of 97 unsold gasoline 'retest the gasoline vehicle on the general road at a fixed speed The number of kilometers to rest, the number of kilometers obtained is 350 kilometers. (Results) From the above results, the additive of Example 3 can increase the number of kilometers that can be driven by a gasoline vehicle from 350 km to 45 [ [Example 4] (test) - 2.5 g of 2 • isobutylcyclohexane The additive of Example 4 was prepared by adding alcohol to 6 liters of % error free gasoline. ‘·’,.

將實施例4的添加劑加入一汽油車奥迪A8〇(排氣 量為2000C.C.,馬力為1?5邱’ 2〇〇2年ι〇月出 廢)的空油箱中’於—般道路上不定速行歇測試 該汽油車可行駛之公里數,獲得之公里數為46〇 公里^ (測試地點為大陸深圳) (空白試驗)使用上述測試的同一汽油車,並於其空油箱 中加入60公升的95無鉛汽油, *車於-般道路上不定速可行故之公丨:: 獲得之公里數為350公里。 (結果) 由上述結果可知,實施例4的添加劑可讓汽油車 可行駛之公里數由350公里提昇至460公里。 [實施例5】 將2.5公克的2_異丁基環己酮加入50公升的97無鉛 汽油中,製得實施例5之添加劑。 …° (測試)冑實施例5的添加劑加入一汽油車本田雅哥(排氣 $為3000C.C.,馬力為2〇〇hp,2〇〇3年6月出廠) 21 201219555 的空油箱中,於一般道路上不定速行駛測試該 汽油車可行駛之公里數,獲得之公里數為440公 里。(測試地點為大陸深圳) (空白試驗)使用上述測試的同一汽油車,並於其空油箱 中加入50公升的97無鉛汽油,再測試該汽 油車於一般道路上不定速可行駛之公里數, 獲得之公里數為350公里。 (結果)自上述結果可知,實施例5的添加劑可讓汽油車 可行駛之公里數由350公里提昇至44〇公里。Adding the additive of Example 4 to the empty tank of a gasoline car Audi A8〇 (with a displacement of 2000C.C., a horsepower of 1?5 Qiu '2〇〇2 years ι〇月) The number of kilometers that the petrol car can travel is tested on the speed limit, and the number of kilometers obtained is 46〇 km ^ (test location is Shenzhen, China) (blank test) using the same gasoline car tested above, and in its empty fuel tank Add 60 liters of 95 unleaded petrol, *The car is not allowed to speed on the road - the number of kilometers is 350 kilometers. (Results) From the above results, the additive of Example 4 can increase the number of kilometers that a gasoline vehicle can travel from 350 km to 460 km. [Example 5] An additive of Example 5 was obtained by adding 2.5 g of 2-isobutylcyclohexanone to 50 liter of 97 unleaded gasoline. ...° (test) 添加剂 The additive of Example 5 was added to a gasoline vehicle Honda Yage (exhaust $ 3000C.C., horsepower 2 hp, 2 〇〇 3 years in June) 21 201219555 in the empty fuel tank The number of kilometers that the gasoline vehicle can travel is tested at a fixed speed on a general road, and the number of kilometers obtained is 440 kilometers. (Test location is Shenzhen, China) (Blank test) Use the same gasoline vehicle tested above, and add 50 liters of 97 unleaded gasoline to its empty fuel tank, and test the number of kilometers that the gasoline vehicle can travel at a fixed speed on a general road. The number of kilometers obtained is 350 kilometers. (Results) From the above results, the additive of Example 5 can increase the number of kilometers that a gasoline vehicle can travel from 350 kilometers to 44 kilometers.

[實施例6J 將2.5公克的4,7,7_三甲基雙環[22 ^庚醇加入%公 升的97無鉛汽油中’製得實施例6之添加劑。 (測試)冑實施例6的添加劑加人-汽油車本田雅哥(排氣 量為3000C.C.,馬力為2〇〇hp,2003年6月出廠) 的空油箱中,於一般道路上不定速行駛,測試該 汽油車可行駛之公里數,獲得之公里數為47〇公 里。(測試地點為大陸深圳) (空白試驗)使用上述測試的同一汽油車,並於其空油箱 中加入50公升的97無紹汽油,再測試該汽 油車於一般道路上不定速可行駛之公里數, 獲得之公里數為350公里。 (結果)&上述結果可知,實施例6的添加劑可讓汽油車 可行駛之公里數由350公里提昇至47〇公里。[Example 6J An additive of Example 6 was prepared by adding 2.5 g of 4,7,7-trimethylbicyclo [22 ^heptanol to % liter of 97 unleaded gasoline]. (Test) 胄 The additive of the example 6 is added to the empty fuel tank of the gasoline-powered Honda Yage (3000 C.C., horsepower 2 hp, factory delivered in June 2003), not on the general road. At a fixed speed, test the number of kilometers that the gasoline car can travel, and the number of kilometers obtained is 47 kilometers. (Test location is Shenzhen, China) (Blank test) Use the same gasoline vehicle tested above, and add 50 liters of 97 non-salted gasoline to its empty fuel tank, and then test the gasoline vehicle to travel at a fixed speed on the general road. The number of kilometers obtained is 350 kilometers. (Results) & The above results show that the additive of Example 6 can increase the number of kilometers that a gasoline vehicle can travel from 350 kilometers to 47 kilometers.

[實施例7J 22 201219555 將2,5公克的4,7,7-三甲基雙環[叫庚嗣加入50公 升的市售柴油中’製得實施例7之添加劑。 (測試)將實施例7的添加劑加入—柴油車TUCS嶋_ M2(排氣量為2〇〇〇C.C.,馬力為136hp,2007年 U月出廠)的空油箱中,於-般道路上不定速行 駛,測試該柴油車可行驶之公里數,獲得之公里 數為590公里。(測試地點為大陸深圳)[Example 7J 22 201219555 An additive of Example 7 was prepared by adding 2,5 g of 4,7,7-trimethylbicyclo [called gadolinium to 50 liters of commercially available diesel oil]. (Test) Adding the additive of Example 7 to the empty fuel tank of diesel vehicle TUCS嶋_ M2 (exhaust volume 2〇〇〇CC, horsepower 136hp, factory delivery in 2007), uncertain on the road Drive at speed and test the number of kilometers that the diesel car can travel. The number of kilometers obtained is 590 kilometers. (Test location is Shenzhen, China)

(空白試驗)冑用上述測試的同一柴油車,並於其空油箱 中加入50公升的柴油,再測試該柴油車於 一般道路上不定速可行駛之公里數,獲得之 公里數為480公里。 (結果)纟上述結果可知,實施例7的添加劑可讓柴油車 可打駛之公里數由480公里提昇至59〇公里。 亦上所述,本發明一種用於提昇液態燃料燃燒效率的 添加劑,藉由添加劑中的可昇華有機化合物,以昇華體積 膨脹的物理現象造成液態燃料授動,讓液態燃料可以均勾 受熱而轉化為小分子或氣態分子,進而使該液態燃料之燃 燒效岸明顯上升,以讓液態燃料充分運用,達到兼顧環保 與省油的目的。 ' .惟以上所述者,僅為本發明之較佳實施例而已,當不 月&以此限定本發B月實施之範圍,即大凡依本發明申請專利 範圍及發明說明内容所作之簡單的等效變化與修飾,皆仍 屬本發明專利涵蓋之範圍内。 23 201219555 【圖式簡單說明】 201219555 【主要元件符號說明】 無(Blank test) The same diesel vehicle tested above was used, and 50 liters of diesel oil was added to its empty fuel tank, and the number of kilometers that the diesel vehicle was able to travel at a fixed speed on a general road was tested. The number of kilometers obtained was 480 km. . (Results) As can be seen from the above results, the additive of Example 7 can increase the number of kilometers that a diesel vehicle can drive from 480 kilometers to 59 kilometers. In addition, the present invention relates to an additive for improving the combustion efficiency of a liquid fuel, which can be converted by a physical phenomenon of sublimation volume expansion by a sublimable organic compound in the additive, so that the liquid fuel can be transformed by heat. It is a small molecule or a gaseous molecule, which in turn makes the combustion effect of the liquid fuel rise significantly, so that the liquid fuel can be fully utilized to achieve environmental protection and fuel economy. The above is only the preferred embodiment of the present invention, and the scope of the implementation of the present invention is limited, and the simplicity of the invention is based on the scope of the invention and the description of the invention. Equivalent variations and modifications are still within the scope of the invention. 23 201219555 [Simplified illustration] 201219555 [Explanation of main component symbols]

2525

Claims (1)

201219555 七、申請專利範圍: 1· 一種用於提昇液態燃料燃燒效率的添加劑,包含。 昇華有機化合物及-液態燃料,其中,該可昇華: 合物在一大氣壓及45t以下為固態。 2. 根據巾請專利範圍第丨項所述之添加劑,其中,該 華有機化合物含有—骨架,該骨架是選自於雙環庚貌、 萘、二氮節、°比喃鋼、環丙烧、環丁燒、環戊燒、環己 烧'環庚烷、環辛烷或苯。 " 3. 根據申請專利範圍第2項所述之添加劑其中,該可昇 華有機化合物是選自於樟腦、萘、薄荷醇、茨醇、茇 稀、第三丁基環己醇、麥芽酚、5_乙醯基-丨丄^^ 甲基二氫節、4-乙醯基-6_第三丁基_^•二甲基二氫節、、 1,1,4’4-四甲基_6_乙基_7_乙醯基_12,3,4_四氫萘、卜萘甲 越0_萘乙謎、2_異丙基-2,5-二經基-5-甲基環己酮、1_ 甲基-1-羥基-4-(1-甲基-1-羥基乙基)環己烷、2_甲基羥 基-5-經基-5-(1 -甲基乙稀基)_2_環己酮、3_甲基_3_經基-6-異丙基-環己酮、5_羥基_5_曱基_2_(丨_甲基亞乙基)環己 烷、2-羥基_2,6,6-三甲基雙環[3.1.1]_2-庚烷、2-(4-羥基- 4-甲基-1-環己院基)異丙醇、卜經基甲基_4_(1_甲基亞 乙基)環己烷、1-甲基-2,5-二異丁基-4-異丙基苯、1-羥 基-2-異丁基環己烧、丨_羥基-丨_異丁基環己烧、丨,4_二羥 基-3,6-二異丁基環己烧、ι_經基_3,6_二異丁基環己烧、 1-經基-4-異丁基環己烷、4,7,7-三甲基雙環[221]庚酮、 4,7,7-三曱基雙環[m]庚醇、卜羥基_3-異丙基_6-曱基 26 201219555 %己烷、2-異了基-3-異丙基環丙酮、2_異丁基_3_異丙基 環丙醇、2-異丁基_4_乙基環丁_、2_異丁基_4_乙基環丁 醇、2-異丁基_4_曱基環戊酮、2_異丁基_4_甲基環戊醇、 異丙基環己酮、2-異丙基環己醇、4•異丙基環庚酮、4· 異丙基環庚醇、3,7-二甲基環辛酮、3,7_二子基環辛醇, 或上述可昇華有機化合物的 一組合。 4.根據申請專利範圍第3項所述之添加劑,其中,該可昇 華有機化合物是選自於薄荷醇、茨醇、茨烯、第三丁基 • 環己醇、麥芽酚、5-乙醯基-1,1,2,3,3,6·六甲基二氫節、 4-乙醯基-6-第三丁基-1,ι_二甲基二氫茚、丨,四曱 基_6-乙基-7-乙醯基-1,2,3,4-四氫萘、0_萘曱醚、3_萘4 醚、2·異丙基-2,5-二羥基-5-曱基環己酮、1-曱基羥 基-4-(1-甲基-1-羥基乙基)環己烷、2_曱基·3羥基_5_羥 基-5-(1-曱基乙烯基)_2-環己酮、3-曱基-3-羥基-6-異丙 基-環己酮、5-羥基-5 -甲基-2-(1-曱基亞乙基)環己院、2_ 备基-2,6,6-三曱基雙環[3.1.1]-2-庚院、2-(4-經基-4-曱 ® 基-1-環己烷基)異丙醇、1-羥基-1-甲基-4-(1-曱基亞乙基) 環己院、1-甲基-2,5-二異丁基-4-異丙基苯、1-經基_2_異 丁基環己烷、1-羥基-1-異丁基環己烷、1,4-二羥基_3,6_ 二異丁基環己烷、1-羥基-3,6-二異丁基環己烷、i_羥基_ 4_異丁基環己烷、4,7,7-三甲基雙環[2.2.1]庚酮、4,7,7-三曱基雙環[2.2.1]庚醇、1-羥基-3-異丙基-6-甲基環己 烷、2-異丁基-3-異丙基環丙酮、2-異丁基-3-異丙基環丙 醇、2-異丁基-4-乙基環丁酮、2-異丁基-4-乙基環丁醇、 27 201219555 2-異丁基_4_曱基環戊酮、入異丁基·4_曱基環戊醇、2_異 丙基環己酮、2_異丙基環己醇、4_異丙基環庚酮、4_異 丙基環庚醇、3,7_二甲基環辛酮、3,7·二甲基環辛醇,或 上述可昇華有機化合物的一組合。 5.根據申請專利範圍第1項所述之添加劑,其中,每 升的液態燃料添加0.5〜5 00公克的可昇華有機化合物。 6·根據申請專利範圍第1項所述之添加劑,其中,該液態 燃料是選自於汽油、柴油、酒精、生質汽油、生質柴 '由、生質酒精、有機氫化燃料油或上述燃料之一組合。 7. —種用於提昇液態燃料燃燒效率的方法,是透過將一可 昇華有機化合物加入一液態燃料中而完成,其中,該可 昇華有機化合物在一大氣壓及45。(:以下為固態。 8. 根據中請專利範圍帛7項所述之方法,其巾,該可昇華 有機化合物含有—骨架,該骨架是選自於雙環[2.2.1]庚 ! '萘、二氫節、吡喃酮、環丙烷、環丁烷、環戊烷、 壞己烷、環庚烷、環辛烷或苯。 9·根據中請專利範圍第8項所述之方法,其中,該可昇華 有機化合物是選自於樟腦、萘、薄荷醇、茨醇 、 第^基環己醇、麥芽齡、5_乙酿基十…从六甲基 一氫印、4-乙醯基_6_第三 ,,,, 土 i,1·一甲基二氫茚、 ,1,4,4-四曱基乙基_7乙醯 ,今3,4-四虱萘、β-萘曱 醚、13-萘乙醚、2_異丙基_2 甲其,t I , &暴-5-甲基環己_、1_ 1 =基Μ·曱基小經基乙基)環己烧、2-甲基_3_經 基-5-經基- 5- (1-甲其法其、。 甲基乙席基)-2-¾己_、3.甲基_3,基_ 28 201219555 6-異丙基-環己酮、5-羥基_5_曱基_2-(l-曱基亞乙基)環己 烷、2-羥基-2,6,6-三甲基雙環[3丄丨卜之-庚烷、2-(4-羥基_ 4-曱基-1-環己烧基)異丙醇、丨_羥基_丨_甲基甲基亞 乙基)環己烷、1-甲基-2,5-二異丁基-4-異丙基苯、丨_羥 基-2-異丁基環己烷、1_羥基_丨_異丁基環己烷、丨,4二羥 基-3,6-二異丁基環己烷、丨_羥基_3,6_二異丁基環己烷、 1- 羥基-4-異丁基環己烷、4,7,7-三甲基雙環[2.2.1]庚酮、 4’7,7 -二甲基雙環[2.2.1]庚醇、經基_3_異丙基_6_甲基 環己烷、2-異丁基-3-異丙基環丙酮、2-異丁基-3-異丙基 環丙醇、2·異丁基-4-乙基環丁酮、2-異丁基-4-乙基環丁 醇、2-異丁基-4-曱基環戊酮、2-異丁基-4-甲基環戊醇、 2- 異丙基環己gig、2-異丙基環己醇、4-異丙基環庚酮、 異丙基環庚醇、3,7-二甲基環辛酮、3,7-二曱基環辛醇, 或上述可昇華有機化合物的一組合。 10.根據申請專利範圍第9項所述之方法,其中,該可昇華 有機化合物是選自於薄荷醇、茨醇 '茨烯、第三丁基環 己醇、麥芽酚、5_乙醯基“山2,3,3,6_六甲基二氫茚、扣 乙醯基-6-第三丁基·M-二曱基二氫茚、四曱基_ 6-乙基-7-乙醯基-i,2,3,4-四氫萘、β·萘曱醚、β-萘乙醚、 2-異丙基-2,5 - 一經基-5-甲基環己酮、ι_甲基_ι_經基 (1-曱基-1-羥基乙基)環己烷、2_甲基_3_羥基_5_羥基 (1-曱基乙烯基)-2-環己酮、3-甲基_3_羥基_6_異丙基_環己 酮、5-羥基-5-甲基_2_(1•曱基亞乙基)環己烷、2_羥基一 2,6,6-二曱基雙環[3.1.1]_2-庚院、2-(4_經基-4-甲基-1_環 29 201219555 己炫基)異丙醇、1-羥基-1-曱基-4-(1-甲基亞乙基)環己. 烧 1甲基-2,5 -二異丁基-4-異丙基苯、1-經基-2-異丁基 環己烧、羥基-1-異丁基環己烷、1,4-二羥基-3,6-二異 丁基環己烷、1-羥基-3,6-二異丁基環己烷、1-羥基_4_異 丁基環己烷、4,7,7-三甲基雙環[2.2.1]庚酮、4,7,7-三甲 基雙環[2.2.1]庚醇、ι_輕基-3-異丙基_6_曱基環己烧、2_ 異丁基-3-異丙基環丙酮、2-異丁基_3_異丙基環丙醇、2_ 異丁基-4-乙基環丁酮、2-異丁基-4-乙基環丁醇、2_異丁 基-4-甲基環戊酮、2_異丁基_4_甲基環戊醇、2_異丙基環 己酮、2-異丙基環己醇、4_異丙基環庚酮、仁異丙基環 _ 庚醇、3,7-二甲基環辛酮、3,7_二曱基環辛醇,或上述可 昇華有機化合物的一組合。 11. 根據申請專利範圍第7項所述之方法,装φ,, Λ 六丫,母10公升 的液態燃料添加0.5〜500公克的可昇華有機化人物 12. 根據申請專利範圍第7項所述之方法,i^ ,、甲,该液態燃 料是選自於汽油、柴油、酒精、生質汽油、生質柴油、 生質酒精、有機氫化燃料油或上述燃料之组人。 30201219555 VII. Patent application scope: 1. An additive for improving the combustion efficiency of liquid fuels, including. Sublimation of organic compounds and liquid fuels, wherein the sublimable compound is solid at atmospheric pressure and below 45t. 2. The additive according to the invention of claim 2, wherein the organic compound comprises a skeleton selected from the group consisting of a bicyclic gemstone, a naphthalene, a dinitrogenate, a bismuth steel, a cyprodinil, Cyclobutane, cyclopentane, cyclohexane, 'cycloheptane, cyclooctane or benzene. " 3. The additive according to claim 2, wherein the sublimable organic compound is selected from the group consisting of camphor, naphthalene, menthol, benzyl alcohol, hydrazine, tert-butylcyclohexanol, maltol , 5_乙醯基-丨丄^^ methyl dihydrogen, 4-ethyl fluorenyl-6_t-butyl _^• dimethyl dihydrogen, 1,1,4'4-tetra _6_Ethyl_7_Ethyl fluorenyl _12,3,4_tetrahydronaphthalene, praline, 0-naphthalene, mystery, 2, isopropyl-2,5-diyl-5- Cyclohexanone, 1-methyl-1-hydroxy-4-(1-methyl-1-hydroxyethyl)cyclohexane, 2-methylhydroxy-5-carbyl-5-(1-methylethyl Dilute)_2_cyclohexanone, 3-methyl_3_carbyl-6-isopropyl-cyclohexanone, 5-hydroxy_5_indolyl_2_(丨_methylethylidene)cyclohexane Alkane, 2-hydroxy-2,6,6-trimethylbicyclo[3.1.1]_2-heptane, 2-(4-hydroxy-4-methyl-1-cyclohexyl)isopropanol, Methyl 4-(1-methylethylidene)cyclohexane, 1-methyl-2,5-diisobutyl-4-isopropylbenzene, 1-hydroxy-2-isobutylcyclohexane , 丨 hydroxy-oxime-isobutylcyclohexanthene, hydrazine, 4_dihydroxy-3,6-diisobutylcyclohexene, iota-based _3,6-diisobutylcyclohexene, 1 -transyl-4-isobutylcyclohexane, 4,7,7-trimethylbicyclo[221]heptanone, 4,7,7-trimercaptobicyclo[m]heptanol, hydroxyl-3 Isopropyl_6-fluorenyl 26 201219555 % hexane, 2-iso-yl-3-isopropylcyclopropanone, 2-isobutyl-3-Isopropylcyclopropanol, 2-isobutyl-4 _Ethylcyclobutane, 2-isobutyl-4-Icyclobutanol, 2-isobutyl-4-indolylcyclopentanone, 2-isobutyl-4-methylcyclopentanol, different Propylcyclohexanone, 2-isopropylcyclohexanol, 4 isopropylcycloheptanone, 4·isopropylcycloheptanol, 3,7-dimethylcyclooctanone, 3,7-diyl Cyclooctanol, or a combination of the above sublimable organic compounds. 4. The additive according to claim 3, wherein the sublimable organic compound is selected from the group consisting of menthol, sterol, benzyl, tert-butyl, cyclohexanol, maltol, 5-B. Mercapto-1,1,2,3,3,6·hexamethyldihydrogen, 4-ethinyl-6-t-butyl-1, ι-dimethyldihydroanthracene, anthracene, tetraterpene _6-Ethyl-7-ethenyl-1,2,3,4-tetrahydronaphthalene, 0-naphthyl ether, 3-naphthyl 4-ether, 2·isopropyl-2,5-dihydroxy- 5-decylcyclohexanone, 1-mercaptohydroxy-4-(1-methyl-1-hydroxyethyl)cyclohexane, 2-mercapto-3hydroxyl-5-hydroxy-5-(1-oxime Vinyl) 2 -cyclohexanone, 3-mercapto-3-hydroxy-6-isopropyl-cyclohexanone, 5-hydroxy-5-methyl-2-(1-indenylethylene) ring己院, 2_备基-2,6,6-trimercaptobicyclo[3.1.1]-2-Gengyuan, 2-(4-pyrimidin-4-indole-1-ylhexyl) Propyl alcohol, 1-hydroxy-1-methyl-4-(1-mercaptoethylene) cyclohexyl, 1-methyl-2,5-diisobutyl-4-isopropylbenzene, 1- Base 2-isobutylcyclohexane, 1-hydroxy-1-isobutylcyclohexane, 1,4-dihydroxy-3,6-diisobutylcyclohexane, 1-hydroxy-3,6 -diisobutylcyclohexane, i_hydroxy_ 4_isobutyl Cyclohexane, 4,7,7-trimethylbicyclo[2.2.1]heptanone, 4,7,7-trimercaptobicyclo[2.2.1]heptanol, 1-hydroxy-3-isopropyl -6-methylcyclohexane, 2-isobutyl-3-isopropylcyclopropanone, 2-isobutyl-3-isopropylcyclopropanol, 2-isobutyl-4-ethylcyclobutane Ketone, 2-isobutyl-4-ethylcyclobutanol, 27 201219555 2-isobutyl-4-indolylcyclopentanone, isobutyl-4-indolylcyclopentanol, 2-isopropyl Cyclohexanone, 2-isopropylcyclohexanol, 4-isopropylcycloheptanone, 4-isopropylcycloheptanol, 3,7-dimethylcyclooctanone, 3,7·dimethyl ring Octanol, or a combination of the above sublimable organic compounds. 5. The additive according to claim 1, wherein 0.5 to 500 grams of the sublimable organic compound is added per liter of the liquid fuel. 6. The additive according to claim 1, wherein the liquid fuel is selected from the group consisting of gasoline, diesel, alcohol, biomass gasoline, biomass, biomass alcohol, organic hydrogenated fuel oil or the like One combination. 7. A method for increasing the combustion efficiency of a liquid fuel by adding a sublimable organic compound to a liquid fuel, wherein the sublimable organic compound is at atmospheric pressure and 45. (The following is a solid state. 8. According to the method described in the scope of claim 7, the towel, the sublimable organic compound contains a skeleton selected from the group consisting of bicyclo [2.2.1] g! Dihydrogen, pyranone, cyclopropane, cyclobutane, cyclopentane, hexane, cycloheptane, cyclooctane or benzene. 9. The method of claim 8, wherein The sublimable organic compound is selected from the group consisting of camphor, naphthalene, menthol, benzyl alcohol, hexylcyclohexanol, malt aging, 5 ethene, hexamethyl hydride, 4-ethyl fluorenyl _6_third,,,, soil i,1·monomethylindoline, 1,4,4-tetradecylethyl _7 acetamidine, present 3,4-tetradecylnaphthalene, β-naphthalene Ethyl ether, 13-naphthyl ether, 2_isopropyl-2-methyl, t I , & violent-5-methylcyclohexyl, 1_ 1 = fluorenyl fluorenyl hydrazine , 2-methyl_3_carbyl-5-carbyl- 5- (1-methodyl, methyl ethyl)-2-3⁄4hexyl, 3.methyl-3-, _ 28 201219555 6-isopropyl-cyclohexanone, 5-hydroxy-5-indenyl-2-(l-decylethylene)cyclohexane, 2-hydroxy-2,6,6-trimethylbicyclo[ 3丄丨卜之-庚, 2-(4-hydroxy-4-cyclodecyl-1-cyclohexanyl)isopropanol, hydrazine-hydroxy-hydrazine-methylmethylethylidene)cyclohexane, 1-methyl-2,5 -diisobutyl-4-isopropylbenzene, hydrazine-hydroxy-2-isobutylcyclohexane, 1-hydroxy-oxime-isobutylcyclohexane, hydrazine, 4 dihydroxy-3,6-di Isobutylcyclohexane, hydrazine-hydroxy-3,6-diisobutylcyclohexane, 1-hydroxy-4-isobutylcyclohexane, 4,7,7-trimethylbicyclo[2.2.1 Heptone, 4'7,7-dimethylbicyclo[2.2.1]heptanol, benzyl-3-ylisopropyl-6-methylcyclohexane, 2-isobutyl-3-isopropyl Cyclopropanone, 2-isobutyl-3-isopropylcyclopropanol, 2·isobutyl-4-ethylcyclobutanone, 2-isobutyl-4-ethylcyclobutanol, 2-isobutyl 4-mercaptocyclopentanone, 2-isobutyl-4-methylcyclopentanol, 2-isopropylcyclohexane gig, 2-isopropylcyclohexanol, 4-isopropylcycloheptanone , isopropylcycloheptanol, 3,7-dimethylcyclooctanone, 3,7-didecylcyclooctanol, or a combination of the above sublimable organic compounds. 10. The method according to claim 9, wherein the sublimable organic compound is selected from the group consisting of menthol, benzyl alcohol, tert-butylcyclohexanol, maltol, and 5 acetamidine. "Mountain 2,3,3,6_hexamethylindoline, ketoxime-6-t-butyl-M-diindenyldihydroanthracene, tetradecyl- 6-ethyl-7- Ethyl-i,2,3,4-tetrahydronaphthalene, β-naphthyl ether, β-naphthyl ether, 2-isopropyl-2,5-mono-yl-5-methylcyclohexanone, ι_ Methyl_ι_trans (1-mercapto-1-hydroxyethyl)cyclohexane, 2-methyl-3-hydroxy-5-hydroxy(1-mercaptovinyl)-2-cyclohexanone, 3-methyl_3_hydroxy_6_isopropyl-cyclohexanone, 5-hydroxy-5-methyl_2_(1•decylethylene)cyclohexane, 2-hydroxy- 2,6, 6-dimercaptobicyclo[3.1.1]_2-gengyuan, 2-(4-di--4-yl-1_cyclo 29 201219555 hexyl) isopropanol, 1-hydroxy-1-indenyl 4-(1-methylethylidene)cyclohexane. 1-methyl-2,5-diisobutyl-4-isopropylbenzene, 1-yl-2-isobutylcyclohexene, Hydroxy-1-isobutylcyclohexane, 1,4-dihydroxy-3,6-diisobutylcyclohexane, 1-hydroxy-3,6-diisobutylcyclohexane, 1-hydroxyl 4_Idin Cyclohexane, 4,7,7-trimethylbicyclo[2.2.1]heptanone, 4,7,7-trimethylbicyclo[2.2.1]heptanol, iota-light-3-isopropyl Base_6_fluorenylcyclohexane, 2_isobutyl-3-isopropylcyclopropanone, 2-isobutyl-3-isopropylidene propanol, 2-isobutyl-4-ethylcyclobutanone , 2-isobutyl-4-ethylcyclobutanol, 2-isobutyl-4-methylcyclopentanone, 2-isobutyl-4-methylcyclopentanol, 2-isopropylcyclohexane Ketone, 2-isopropylcyclohexanol, 4-isopropylcycloheptanone, isopropylcyclo-heptanol, 3,7-dimethylcyclooctanone, 3,7-didecylcyclooctanol , or a combination of the above sublimable organic compounds. 11. According to the method described in claim 7, the φ, Λ 丫 丫, mother 10 liters of liquid fuel is added 0.5 to 500 gram of sublimable organic characters 12. According to the method described in claim 7, i?, A, the liquid fuel is selected from the group consisting of gasoline, diesel, alcohol, biomass gasoline, biodiesel, bio-alcohol, organic hydrogenated fuel oil or The group of the above fuels. 30
TW099138652A 2010-11-10 2010-11-10 promoting the Brownian motion by the addition of a sublimatable organic compound TW201219555A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
TW099138652A TW201219555A (en) 2010-11-10 2010-11-10 promoting the Brownian motion by the addition of a sublimatable organic compound
US13/200,274 US20120110900A1 (en) 2010-11-10 2011-09-22 Liquid fuel composition and method for enhancing combustion efficiency of a liquid fuel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
TW099138652A TW201219555A (en) 2010-11-10 2010-11-10 promoting the Brownian motion by the addition of a sublimatable organic compound

Publications (1)

Publication Number Publication Date
TW201219555A true TW201219555A (en) 2012-05-16

Family

ID=46018300

Family Applications (1)

Application Number Title Priority Date Filing Date
TW099138652A TW201219555A (en) 2010-11-10 2010-11-10 promoting the Brownian motion by the addition of a sublimatable organic compound

Country Status (2)

Country Link
US (1) US20120110900A1 (en)
TW (1) TW201219555A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015115880A1 (en) * 2014-01-30 2015-08-06 Torres Roldán Victor Enrique Composition for fuels
US20150259619A1 (en) * 2014-03-11 2015-09-17 Swift Fuels, Llc Motor fuel formulation
US11149224B2 (en) * 2017-11-17 2021-10-19 Dorf Ketal Chemicals Fze Fuel additive compositions, and method of use thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2012945A (en) * 1932-04-16 1935-09-03 Du Pont Motor fuel
WO2010017099A2 (en) * 2008-08-05 2010-02-11 Spirit Of The 21St Century Group,Llc Modified fuels and methods of making and using thereof

Also Published As

Publication number Publication date
US20120110900A1 (en) 2012-05-10

Similar Documents

Publication Publication Date Title
Laszlo Catalysis of organic reactions by inorganic solids
Brown et al. Selective reductions. XIII. Reaction of 2-cyclopentenones with representative complex hydrides. Aluminum hydride as a selective reagent for the reduction of the carbonyl group in 2-cyclopentenones
Bailón-García et al. Catalysts supported on carbon materials for the selective hydrogenation of citral
US10738253B2 (en) Bio-nano emulsion fuel
TW201219555A (en) promoting the Brownian motion by the addition of a sublimatable organic compound
US8779014B2 (en) Slurry catalyst and the preparation thereof
CN102247852A (en) Cu-Fe-Co base catalyst used for synthesizing low carbon alcohol by utilizing synthesis gas as well as preparation method and application thereof in low carbon alcohol synthesizing process by virtue of synthesis gas
JP2022509550A (en) Equipment for collecting volatile organic compounds
Fan et al. Effect of organic additives on partial hydrogenation of benzene
Nanda et al. Selective hydrogenolysis of glycerol and crude glycerol (a by-product or waste stream from the biodiesel industry) to 1, 2-propanediol over B2O3 promoted Cu/Al2O3 catalysts
Peng et al. Magnetic graphene oxide supported tin oxide (SnO) nanocomposite as a heterogeneous catalyst for biodiesel production from soybean oil
CN107754853B (en) A coordination compound of amino-modified SiO2 microspheres, its preparation method and application
CN102690170B (en) Method for preparing ethanol by acetic acid gas phase hydrogenation
Dou et al. Hydrodeoxygenation of furfural to 2-methylfuran over Cu-Co confined by hollow carbon cage catalyst enhanced by optimized charge transfer and alloy structure
CN103804145B (en) A kind of preparation method of 3-methyl-3-butene-1-alcohol
Wang et al. Recent progress of hydrogenation and hydrogenolysis catalysts derived from layered double hydroxides
CN102351663B (en) Synthesis method of eugenol methyl ether
CN102465045A (en) Additives and methods for improving combustion efficiency of liquid fuels
Brunner et al. Configurational assignment of ‘cryptochiral’10‐hydroxystearic acid through an asymmetric catalytic synthesis
CN101884925A (en) A kind of α-pinene hydrogenation synthesis pinane catalyst and preparation method
CN101898156B (en) Preparation of Cobalt(ii) Porphyrin Catalysts Supported by CeO2-doped Organosilicon Nanospheres
CN109833906A (en) Bifunctional catalyst for preparing low-condensation-point biodiesel and preparation method and application thereof
CN104399529B (en) A kind of alkadienes selective hydrocatalyst and preparation method and application
Fan et al. Recent Advances in Light‐Induced Carboxylation of Organic (Pseudo) Halides with CO2
CN107469844A (en) A kind of deoxidation method of hydrotreating of catalyst with deoxidation hydrogenating function and preparation method thereof and carbonyls