WO2009113080A1 - Velar bio hydrocarbon fuel - Google Patents
Velar bio hydrocarbon fuel Download PDFInfo
- Publication number
- WO2009113080A1 WO2009113080A1 PCT/IN2008/000258 IN2008000258W WO2009113080A1 WO 2009113080 A1 WO2009113080 A1 WO 2009113080A1 IN 2008000258 W IN2008000258 W IN 2008000258W WO 2009113080 A1 WO2009113080 A1 WO 2009113080A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hydrocarbon fuel
- alcohol
- fuel
- weight
- bio
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/16—Hydrocarbons
- C10L1/1608—Well defined compounds, e.g. hexane, benzene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/1811—Organic compounds containing oxygen peroxides; ozonides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/1822—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
- C10L1/1824—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
Definitions
- This invention in general relates to Energy Saving Technology. Further, this invention relates to manufacture of Novel Fuels. More particularly, this invention relates to production of hydrocarbon fuel from a bio-mass.
- Gasoline is used as fuel all over the world for Engines. Consumption of the Fuel is increasing day by day. Its sources are limited and will vanish in the near Future. Further, there is a problem of Environmental Pollution. Due to increase in the number of vehicles, the consumption of fuel has increased resulting in increasing polluting emissions. It is the need of the time to control pollution by promoting alternative fuel for Motor Vehicles.
- Steps in this regard have been taken in countries like Brazil and India also, wherein Gasoline is blended with Ethanol in varying percentage.
- Herbal products have been used as fuel in one or other form since pre - ancient time. Some of the herbs, rich in oil content such as pine oil, eucalyptus oil etc., fermentation product of mollases ( i.e. alcohol ) are also well known as fuels. Some other herbal products as pinene, dipentene, terpinolene, ordinary turpentine, sulphate turpentine ( 15 % to 25 % ) and volatile aliphatic hydrocarbons render themselves as self igniting liquid fuels oxidant combination for Rockets, with 95 % nitric acid containing 10 % to 30 % oleum.
- Engine Fuel US patent No. 5,501,713 - March 26, 1996 discloses the fuel to be comprised of terpene, alcohol and lubricating oil where limonene did not exceed 50 %.
- Engine fuel ( US patent No. 5,575,822 - November 19, 1996 ) discloses the fuel to contain terpene up to 42 % only with 80 % to 90 % of naphtha.
- Engine fuel US patent No. 5,607,486 - March 4, 1997 discloses the engine fuel to contain terpene up to 25 % only with 10 % to 15 % of naphtha and 70 % to 80 % of methanol.
- methanol and naphtha mentioned in the patents at SI. Nos. 3,4 and 5 could't be on a large scale as they are toxic substances.
- the terpene in the present invention is more than 55 % and without toxic ingredients being used.
- This invention relates to the manufacture of a novel kind of hydrocarbon fuel from biomass and a process of producing the said hydrocarbon fuel on a large scale.
- This invention particularly, though not exclusively, will relate to process of reducing the hydrocarbon from C 20 to C 6 straight carbon chain.
- Most of the conventional fuels, viz. petrol, diesel and kerosene are in this range. It is a well known fact that the hydrocarbon fuels are depleting and becoming very scare and expensive. Research and development are directed towards inventing a novel kind of hydrocarbon fuel which will substitute the existing fuel known in the art.
- Leaves - are apically clustered , oblong to lanceolate.
- Calyx - Tube Broadly campanulate, lobes 5-7 triangular. Petals - 5-7, White, Ovate, Saccate at base.
- Terpenoids are organic compounds, which occur in the plant kingdom, obtained from the sap, and tissues of certain plants viz. boswellia and piper cubeba. ISOPRENE RULE
- Terpenoids follow isoprene rule, the carbon skeleton of which can be represented with the help of isoprene rule.
- Boswellia oil containing Terpene hydrocarbons are usually pale yellow in colour and has an agreeable odour.
- the following is the typical composition of the boswellia oil:
- the aforesaid raw materials in their proportion are mixed homogeneously and heated to obtain the hydrocarbon fuel.
- This hydrocarbon fuel can be used as such or the contents of raw materials are heated with aluminium oxide in a vessel. When the heating takes place, the large molecules are broken into smaller molecules. This results in a quality of the hydrocarbon fuel matching that of Aviation Fuel.
- the synergic effect of the various raw materials results in the special quality of the hydrocarbon fuel.
- the emission of carbon monoxide is less compared to conventional hydrocarbon fuels and hence eco- friendly.
- the fuel is obtained from an exclusive bio — source which is available extensively and in plenty on Earth and a hydro y 38 X carbon fuel is a reasonable source of energy is split into lighted material leading to a novel kind of hydro carbon fuel which has extensive application in the area of energy and transportation, wherein subjecting the hydrocarbon fuel.
- Ethyl alcohol is manufactured by fermentation of starch and sugar.
- Methyl Alcohol is manufactured by wood.
- Ethyl Formate is mostly by fermentation water sugarcane base.
- Cyclopentane is prepared from the ethyl esther of adipic acid. Adipic acid is found in beet juice.
- hydrocarbon fuel in accordance with the invention wherein the raw material Glycerine should not exceed 40 % of total weight of the composition.
- the said raw material required heating with Al 2 O 3 in order to obtain the hydrocarbon fuel.
- a novel process of manufacturing the said hydrocarbon fuel in accordance with the invention wherein the aforesaid raw materials are homogeneously mixed in a vessel and optionally heated. In the above process, larger molecules are broken down into smaller ones.
- the invention in general covers the composition of a novel hydrocarbon fuel and a process of manufacturing the said hydrocarbon fuel.
- Ethers are compounds of formula R-O-R 1 , where R and R 1 maybe alkyl groups or aryl ( benzene ring ) groups.
- R and R 1 maybe alkyl groups or aryl ( benzene ring ) groups.
- ethers are related to water, with alkyl groups replacing the hydrogen atoms.
- one hydrogen atom of water is replaced by an alkyl group.
- ether both hydrogen are replaced by alkyl groups.
- the two alkyl groups are the same in a symmetrical ether and different in an unsymmetrical ether.
- Ether is diethyl ether, often called “ethylether”, or simply "ether".
- Ether is a good solvent for reactions and extractions, and it is used as a volatile Starting fluid for diesel and gasoline engines. Ether was used as a surgical anesthetic for over a hundred years ( starting in 1842 ), but it is highly flammable, and patients often vomitted as they regained consciousness.
- nitrous oxide N 2 O
- CF 3 -CHCLBr halothane
- the S N I reaction goes much more readily in polar solvents that stabilize ions.
- the rate- limiting step forms two ions, and ionization is taking place in the transition state.
- Polar solvents solvate these ions by an interaction of the solvent's dipole moment with the charge of the ion.
- Protic solvents such as alcohols and water are even more effective solvents because anions form hydrogen bonds with the - OH hydrogen atom, and cations complex with the nonbonding electrons of the -OH oxygen atom. 8
- Ionization of an alkyl halide requires formation and separation of positive and negative charges, similar to what happens when sodium chloride dissolves in water. Therefore, SNI reactions, require highly polar solvents that strongly solvate ions.
- One measure of a solvent's ability to solvate ions is its dielectric constant g , a measure of the solvent's polarity.
- Table 9-6 lists the dielectric constants of some common solvents and the relative ionization rates for t-butyl chloride in these solvents. Note that ionization occurs much faster in highly polar solvents such as water and alcohols. Although most alkyl halides are not soluble in water, they often dissolve in highly polar mixtures of acetone and alcohols with water.
- a formate ester such as Ethyl Formate, reacts with an excess of a Grignard reagent to give ( after protonation ) secondary alcohols with two identical alkyl groups.
- the catalyst used was Ru, Pt or Rh. and Benzoyl Peroxide.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Liquid Carbonaceous Fuels (AREA)
Abstract
Description
Claims
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2008801292245A CN102083948A (en) | 2008-03-12 | 2008-04-24 | Membrane biohydrocarbon fuel |
| EP08763734A EP2265698A4 (en) | 2008-03-12 | 2008-04-24 | Velar bio hydrocarbon fuel |
| CA2717907A CA2717907A1 (en) | 2008-03-12 | 2008-04-24 | Velar bio hydrocarbon fuel |
| AU2008352537A AU2008352537A1 (en) | 2008-03-12 | 2008-04-24 | Velar bio hydrocarbon fuel |
| US12/922,147 US20110016774A1 (en) | 2008-03-12 | 2008-04-24 | Velar Bio Hydrocarbon Fuel |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN608CH2008 | 2008-03-12 | ||
| IN608/CHE/2008 | 2008-03-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2009113080A1 true WO2009113080A1 (en) | 2009-09-17 |
Family
ID=41064804
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/IN2008/000258 Ceased WO2009113080A1 (en) | 2008-03-12 | 2008-04-24 | Velar bio hydrocarbon fuel |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20110016774A1 (en) |
| EP (1) | EP2265698A4 (en) |
| CN (1) | CN102083948A (en) |
| AU (1) | AU2008352537A1 (en) |
| CA (1) | CA2717907A1 (en) |
| WO (1) | WO2009113080A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010071595A1 (en) * | 2008-12-19 | 2010-06-24 | Sekab Biofuels & Chemicals Ab | Denaturant-containing, ethanol-based liquid |
| WO2012021640A1 (en) * | 2010-08-10 | 2012-02-16 | Best Tech Brands Llc | Diesel fuel combustion enhancing additive |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019038650A1 (en) * | 2017-08-20 | 2019-02-28 | KYEDATORE, M. Mahadevaiah | A bio-hydrocarbon fuel composition and method for preparation thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5501713A (en) * | 1994-05-04 | 1996-03-26 | Wilkins, Jr.; Joe S. | Engine fuels |
| WO2003062354A1 (en) * | 2002-01-21 | 2003-07-31 | Ramar Ponniah | Hydrocarbon fuel |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6042493A (en) * | 1983-08-18 | 1985-03-06 | Honda Motor Co Ltd | Two-cycle engine oil composition |
| US5186722A (en) * | 1991-06-25 | 1993-02-16 | Cantrell Research, Incorporated | Hydrocarbon-based fuels from biomass |
| US5575822A (en) * | 1994-05-04 | 1996-11-19 | Wilkins, Jr.; Joe S. | Engine fuels |
| US5607486A (en) * | 1994-05-04 | 1997-03-04 | Wilkins, Jr.; Joe S. | Engine fuels |
| AU3684800A (en) * | 2000-01-24 | 2001-07-31 | Angelica Golubkov | Motor fuel for spark ignition internal combustion engines |
-
2008
- 2008-04-24 WO PCT/IN2008/000258 patent/WO2009113080A1/en not_active Ceased
- 2008-04-24 AU AU2008352537A patent/AU2008352537A1/en not_active Abandoned
- 2008-04-24 EP EP08763734A patent/EP2265698A4/en not_active Withdrawn
- 2008-04-24 CA CA2717907A patent/CA2717907A1/en not_active Abandoned
- 2008-04-24 CN CN2008801292245A patent/CN102083948A/en active Pending
- 2008-04-24 US US12/922,147 patent/US20110016774A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5501713A (en) * | 1994-05-04 | 1996-03-26 | Wilkins, Jr.; Joe S. | Engine fuels |
| WO2003062354A1 (en) * | 2002-01-21 | 2003-07-31 | Ramar Ponniah | Hydrocarbon fuel |
Non-Patent Citations (1)
| Title |
|---|
| See also references of EP2265698A4 * |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010071595A1 (en) * | 2008-12-19 | 2010-06-24 | Sekab Biofuels & Chemicals Ab | Denaturant-containing, ethanol-based liquid |
| WO2012021640A1 (en) * | 2010-08-10 | 2012-02-16 | Best Tech Brands Llc | Diesel fuel combustion enhancing additive |
| US8470058B2 (en) | 2010-08-10 | 2013-06-25 | Best Tech Brands Llc | Diesel fuel combustion enhancing additive |
| JP2013536284A (en) * | 2010-08-10 | 2013-09-19 | ベスト テック ブランズ エルエルシー | Diesel fuel combustion enhancement additive |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2008352537A1 (en) | 2009-09-17 |
| EP2265698A1 (en) | 2010-12-29 |
| US20110016774A1 (en) | 2011-01-27 |
| EP2265698A4 (en) | 2012-03-07 |
| CA2717907A1 (en) | 2009-09-17 |
| CN102083948A (en) | 2011-06-01 |
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