US20080115409A1 - Alternative fuel comprising combustible solids and by-products or waste material from industrial processes - Google Patents

Alternative fuel comprising combustible solids and by-products or waste material from industrial processes Download PDF

Info

Publication number
US20080115409A1
US20080115409A1 US11/561,150 US56115006A US2008115409A1 US 20080115409 A1 US20080115409 A1 US 20080115409A1 US 56115006 A US56115006 A US 56115006A US 2008115409 A1 US2008115409 A1 US 2008115409A1
Authority
US
United States
Prior art keywords
glycerin
liquid hydrocarbon
alternative fuel
combustible
coal
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.)
Abandoned
Application number
US11/561,150
Inventor
Bo L. Tran
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ecolab USA Inc
Original Assignee
Nalco Co LLC
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 Nalco Co LLC filed Critical Nalco Co LLC
Priority to US11/561,150 priority Critical patent/US20080115409A1/en
Assigned to NALCO COMPANY reassignment NALCO COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: TRAN, BO L.
Priority to US11/857,093 priority patent/US20080005956A1/en
Publication of US20080115409A1 publication Critical patent/US20080115409A1/en
Priority to US12/246,975 priority patent/US20090025276A1/en
Priority to US12/356,352 priority patent/US20090127499A1/en
Assigned to BANK OF AMERICA, N.A., AS COLLATERAL AGENT reassignment BANK OF AMERICA, N.A., AS COLLATERAL AGENT SECURITY AGREEMENT Assignors: CALGON LLC, NALCO COMPANY, NALCO CROSSBOW WATER LLC, NALCO ONE SOURCE LLC
Assigned to NALCO COMPANY reassignment NALCO COMPANY RELEASE BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: BANK OF AMERICA, N.A.
Assigned to NALCO COMPANY reassignment NALCO COMPANY RELEASE BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: BANK OF AMERICA, N.A.
Assigned to ECOLAB USA INC. reassignment ECOLAB USA INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CALGON CORPORATION, CALGON LLC, NALCO COMPANY LLC, ONDEO NALCO ENERGY SERVICES, L.P.
Assigned to NALCO COMPANY LLC reassignment NALCO COMPANY LLC CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: NALCO COMPANY
Assigned to ECOLAB USA INC. reassignment ECOLAB USA INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: NALCO COMPANY
Abandoned legal-status Critical Current

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
    • C10L5/00Solid fuels
    • C10L5/40Solid fuels essentially based on materials of non-mineral origin
    • C10L5/44Solid fuels essentially based on materials of non-mineral origin on vegetable substances
    • 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
    • C10L5/00Solid fuels
    • C10L5/02Solid fuels such as briquettes consisting mainly of carbonaceous materials of mineral or non-mineral origin
    • C10L5/06Methods of shaping, e.g. pelletizing or briquetting
    • C10L5/10Methods of shaping, e.g. pelletizing or briquetting with the aid of binders, e.g. pretreated binders
    • C10L5/14Methods of shaping, e.g. pelletizing or briquetting with the aid of binders, e.g. pretreated binders with organic binders
    • 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
    • C10L5/00Solid fuels
    • C10L5/40Solid fuels essentially based on materials of non-mineral origin
    • C10L5/46Solid fuels essentially based on materials of non-mineral origin on sewage, house, or town refuse
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/10Biofuels, e.g. bio-diesel
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/30Fuel from waste, e.g. synthetic alcohol or diesel

Definitions

  • This invention relates to alternative fuels comprising by-products or waste material from industrial processes and methods of using the fuels. More particularly, this invention concerns alternative fuels comprising liquid hydrocarbons derived from biomass and combustible solids.
  • the biomass liquid hydrocarbons can include sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters glycerin and fatty acids.
  • the liquid hydrocarbon is mixed with coal or other combustible solids to prepare the alternative fuel.
  • Biomass presents a promising renewable energy source that could provide an alternative to the use of fossil resources.
  • Biomass includes crops, trees, grasses, crop residues, forest residues, animal wastes, and municipal wastes. There are many reasons to increase the use biomass for energy, including lessening dependence upon foreign oil, utilizing green chemistries from a renewable source, creating less toxic pollution, and improving the domestic agricultural economy.
  • a fuel product formed from vegetable oil and dried cellulosic powder is disclosed in U.S. Pat. No. 6,818,027 B2 and Published Patent Application No. 2005/0055873 A1.
  • a fuel product formed by homogenizing, heating, pressurizing and removing water from organic waste products of industrial processes and then separating a selected constituent from the product into a waste stream and blending the waste stream with a fuel is disclosed in Published Patent Application Publication No. 2005/0142250 A1.
  • U.S. Pat. No. 6,890,451 B2 discloses an anti-icing or deicing fluid comprising by-products of triglyceride processing and its application to surfaces including particulate materials such as coal.
  • a method of preventing the agglomeration of coal in subfreezing temperatures comprising applying an anti-agglomerating amount of by-product glycerin containing up to 5 percent methanol by weight to the coal is disclosed in U.S. Pat. No. 7,108,800.
  • a method of preventing the agglomeration of coal in subfreezing temperatures comprising applying an anti-agglomerating amount of by-product sugar solution to the coal is disclosed in U.S. Pat. No. 6,878,308 B2.
  • the fuel comprises biomass liquid hydrocarbons mixed or blended with existing fuels such as coal and/or other combustible solids.
  • biomass hydrocarbon liquids of this invention are by-products of current processes. For example, fatty acids and glycerin are by-products of a biodiesel manufacturing process.
  • this invention is an alternative fuel comprising one or more combustible solids and one or more liquid hydrocarbon components selected from a group consisting of sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids, provided that when the liquid hydrocarbon component is vegetable oil, the combustible solid is other than a cellulosic powder and further provided that when the combustible solid is coal, the liquid hydrocarbon component is other than sugar solutions.
  • liquid hydrocarbon components selected from a group consisting of sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids
  • this invention is method of preparing a alternative fuel comprising applying one or more liquid hydrocarbon components selected from a group consisting of sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids to one or more combustible solids, provided that when the liquid hydrocarbon component is vegetable oil, the combustible solid is other than a cellulosic powder and further provided that when the combustible solid is coal, the liquid hydrocarbon component is other than sugar solutions.
  • liquid hydrocarbon components selected from a group consisting of sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids
  • the invention uses biomass liquids such as sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids mixed with coal or other combustible solids to create alternative fuels.
  • biomass liquids such as sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids mixed with coal or other combustible solids.
  • the sugar solutions, vegetable oils, animal fats, triglycerides, methyl esters, glycerin and fatty acids described herein are “green”, i.e. non-hazardous, non-toxic, biodegradable, environmentally friendly, and/or derived from renewable sources.
  • Combustible solids means any solid combustible material which can be mixed with one or more biomass liquids as described herein to prepare the alternative fuel of the invention.
  • the combustible solid is selected from coal, wood chips, coke, and garbage.
  • the combustible solid is coal.
  • “Coal” includes fine coal from stockpiles, fine coal from impoundments, run of mine coal washed, run of mine coal unwashed and waste coal. Coke is derived from coal. Garbage includes municipal and/or industrial garbage.
  • “Sugar solutions” refers to by-products of sugar beet or sugar cane processing which can comprise one or more components selected from raffinose, glutamine, betaine, lactate, glucose and/or fructose. Other components can include sodium, potassium, chloride, nitrate, nitrite, acetate, ammonia and magnesium. The by-products are also commonly referred to as “de-sugared” solutions.
  • Black liquor refers to the liquor resulting from the sulfate or kraft paper processes. Black liquor comprises lignin and tall oil.
  • “Tall oil” refers to a mixture of rosin acids, fatty acids including oleic and linoleic acids and other organic material including sterols and long chain alcohols resulting from acid treatment of black liquor as described above.
  • Triglycerides refers to esters of glycerol, a trihydric alcohol, with different fatty acids of varying molecular weight associated with a particular fat or oil. Triglycerides are the principal components of animal fats and vegetable oils. The most common fatty acids sourced from natural fats and oils include palmitic, stearic and linoleic acid.
  • “Fatty acids” means carboxylic acids derived from or contained in an animal or vegetable fat or oil. Fatty acids comprise a terminal COOH group and a long chain saturated or unsaturated alkyl chain. Representative fatty acids include butyric acid, lauric acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, and the like.
  • Glycerin and “glycerol” means 1,2,3-propanetriol.
  • Glycerin and fatty acids can be derived as by-products from transesterification reactions involving triglycerides including transesterification reactions involving biodiesel manufacturing processes as described herein.
  • Methods and “ethyl esters” means methyl and ethyl esters of fatty acids as described herein.
  • “Vegetable oil” means triglycerides extracted from the seeds, fruit or leaves of plants including corn oil, soybean oil, canola oil, palm oil, coconut oil, rapeseed oil, and the like.
  • methyl esters, ethyl esters, glycerin and fatty acids are derived from transesterification reactions involving triglycerides.
  • Transesterification reactions involving triglycerides refers to the splitting of triglyceride esters derived from vegetable oils and/or animal fats in the presence of base and a monohydroxy alcohol such as methanol or ethanol to produce monoesters of the fatty acids comprising the original triglycerides.
  • Representative fats and oils used in the transesterification reactions described herein include tallow, crude tall oil, virgin vegetable oils, soy, mustard, canola, coconut, rapeseed, palm, poultry offal, fish oils, used cooking oils, and/or trap grease, and the like.
  • the glycerin, fatty acids, ethyl esters and methyl esters are derived from a biodiesel manufacturing process.
  • Biodiesel is a cleaner-burning diesel replacement fuel made from natural, renewable sources.
  • biodiesel can include fatty acid alkyl esters used as a cleaner-burning diesel replacement fuel made from sources such as new and used vegetable oils and animal fats.
  • Biodiesel is typically made through a chemical process called transesterification in which vegetable oil or animal fats are converted to fatty acid alkyl esters and glycerin by-products.
  • Fatty acids and fatty acid alkyl esters can be produced from oils and fats by base-catalyzed transesterification of the oil, direct acid-catalyzed esterification of the oil and conversion of the oil to fatty acids and subsequent esterification to biodiesel.
  • fatty acid alkyl esters are produced by the base-catalyzed method.
  • any base may be used as the catalyst used for transesterification of the oil to produce biodiesel, however sodium hydroxide or potassium hydroxide are used in most commercial processes.
  • the oils and fats can be filtered and preprocessed to remove water and contaminants. If free fatty acids are present, they can be removed or transformed into biodiesel using special pretreatment technologies, such as acid catalyzed esterification.
  • the pretreated oils and fats can then be mixed with an alcohol and a catalyst (e.g. base).
  • the base used for the reaction is typically sodium hydroxide or potassium hydroxide, being dissolved in the alcohol used (typically ethanol or methanol) to form the corresponding alkoxide, with standard agitation or mixing. It should be appreciated that any suitable base can be used.
  • the alkoxide may then be charged into a closed reaction vessel and the oils and fats are added. The system can then be closed, and held at about 71° C. (160° F.) for a period of about 1 to 8 hours, although some systems recommend that the reactions take place at room temperature.
  • oil molecules e.g. triglycerides
  • two major products are produced: 1) a crude fatty acid alkyl esters phase (i.e. biodiesel phase) and 2) a glycerin by-product phase.
  • the crude fatty acid alkyl esters phase forms a layer on top of the denser glycerin by-product phase.
  • the glycerin by-product phase is denser than the biodiesel phase, the two can be gravity separated.
  • the glycerin by-product phase can be simply drawn off the bottom of a settling vessel. In some cases, a centrifuge may be employed to speed the separation of the two phases.
  • the glycerin by-product phase typically consists of a mixture of glycerin, methyl esters, methanol, mong and inorganic salts and water.
  • Mong is “matiere organique non glycerol”.
  • Mong normally consists of soaps, free fatty acids, and other impurities.
  • Methyl esters are typically present in an amount of about 0.01 to about 5 percent by weight.
  • Methanol can be present in the glycerin and fatty acids in an amount greater than about 5 weight percent to about 30 weight percent.
  • the methanol can be a valuable component in the alternative fuels because of its low flash point which can help ignite the fuel.
  • glycerin by-product it may be necessary to further refine the glycerin by-product prior to use, for example by washing, acidulation or distillation to adjust the glycerin concentration and/or remove impurities. Methanol may also be added to the desired concentration.
  • the glycerin-containing by-product comprises about 30 to about 95 weight percent of glycerin.
  • the combustible solid is coal and the liquid hydrocarbon component is by-product glycerin.
  • the fatty acid by-products can originate from the refining of the crude fatty acid alkyl esters phase and/or the crude glycerin phase during the biodiesel manufacturing process.
  • the crude fatty acid alkyl esters phase typically includes a mixture of fatty acid alkyl esters, water and a fatty acid salts component.
  • These fatty acid salts component generally form a solution with the water phase (e.g. soap water) where they can be further separated from the fatty acid alkyl esters component.
  • any suitable acid such as, for example, hydrochloric acid can be added to the water phase containing the fatty acid salts component to produce the fatty acid by-products of the present invention.
  • the fatty acid by-product may be in a wax or solid form. It can also contain fatty acid esters. The esters are beneficial components in the alternative fuel mixture.
  • the crude glycerin phase typically includes a mixture of glycerin, water and a fatty acid salts component.
  • This fatty acid salts component forms a solution or suspension with the water phase where it can be further separated from the glycerin component by adding any suitable acid to recover the fatty acid by-products suitable for the present invention.
  • the fatty acid by-products of the present invention can be derived from the acidulation of any of the biodiesel manufacturing process streams/stages that contain the fatty acid salts component (e.g. soap water) including, for example, the wash water.
  • the fatty acid salts component e.g. soap water
  • these fatty acid by-products derived from any of the different stages/streams of the biodiesel manufacturing process can be used as a component in alternative fuel.
  • the alternative fuels are prepared by applying the desired amount of liquid hydrocarbon component to the combustible solid, for example by spraying onto piles of the combustible solid or by means of showers oriented over conveyors used to transport the combustible solid. If desired, the liquid hydrocarbon component-combustible solid mixture may be mixed to ensure even distribution of the liquid hydrocarbon in the combustible solid.
  • the alternative fuel may be prepared by applying the liquid hydrocarbon component to the combustible solid and pressing the resulting material into briquettes or ingots.
  • about 0.1 to about 49 weight percent of said liquid hydrocarbon component is applied to the combustible solid.
  • the alternative fuel of this invention may be used as a substitute for, or additive to conventional combustible solids for combustion in boilers or furnaces.

Abstract

An alternative fuel composition and methods of preparing and using the composition is provided. The alternative fuel can comprise coal, or another combustible solid, and one or more components selected from a group consisting of sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids.

Description

    TECHNICAL FIELD
  • This invention relates to alternative fuels comprising by-products or waste material from industrial processes and methods of using the fuels. More particularly, this invention concerns alternative fuels comprising liquid hydrocarbons derived from biomass and combustible solids. The biomass liquid hydrocarbons can include sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters glycerin and fatty acids. The liquid hydrocarbon is mixed with coal or other combustible solids to prepare the alternative fuel.
  • BACKGROUND OF THE INVENTION
  • The current US economy is dominated by technologies that rely on fossil energy (coal, petroleum, and natural gas) to produce fuels. Biomass presents a promising renewable energy source that could provide an alternative to the use of fossil resources. Biomass includes crops, trees, grasses, crop residues, forest residues, animal wastes, and municipal wastes. There are many reasons to increase the use biomass for energy, including lessening dependence upon foreign oil, utilizing green chemistries from a renewable source, creating less toxic pollution, and improving the domestic agricultural economy.
  • A fuel product formed from vegetable oil and dried cellulosic powder is disclosed in U.S. Pat. No. 6,818,027 B2 and Published Patent Application No. 2005/0055873 A1.
  • A fuel product formed by homogenizing, heating, pressurizing and removing water from organic waste products of industrial processes and then separating a selected constituent from the product into a waste stream and blending the waste stream with a fuel is disclosed in Published Patent Application Publication No. 2005/0142250 A1.
  • U.S. Pat. No. 6,890,451 B2 discloses an anti-icing or deicing fluid comprising by-products of triglyceride processing and its application to surfaces including particulate materials such as coal. A method of preventing the agglomeration of coal in subfreezing temperatures comprising applying an anti-agglomerating amount of by-product glycerin containing up to 5 percent methanol by weight to the coal is disclosed in U.S. Pat. No. 7,108,800. A method of preventing the agglomeration of coal in subfreezing temperatures comprising applying an anti-agglomerating amount of by-product sugar solution to the coal is disclosed in U.S. Pat. No. 6,878,308 B2.
  • SUMMARY OF THE INVENTION
  • This invention relates to a novel and cost effective fuel and methods of preparing and using the fuel. The fuel comprises biomass liquid hydrocarbons mixed or blended with existing fuels such as coal and/or other combustible solids. Some of the biomass hydrocarbon liquids of this invention are by-products of current processes. For example, fatty acids and glycerin are by-products of a biodiesel manufacturing process.
  • Accordingly, in an embodiment, this invention is an alternative fuel comprising one or more combustible solids and one or more liquid hydrocarbon components selected from a group consisting of sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids, provided that when the liquid hydrocarbon component is vegetable oil, the combustible solid is other than a cellulosic powder and further provided that when the combustible solid is coal, the liquid hydrocarbon component is other than sugar solutions.
  • In another embodiment, this invention is method of preparing a alternative fuel comprising applying one or more liquid hydrocarbon components selected from a group consisting of sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids to one or more combustible solids, provided that when the liquid hydrocarbon component is vegetable oil, the combustible solid is other than a cellulosic powder and further provided that when the combustible solid is coal, the liquid hydrocarbon component is other than sugar solutions.
  • DETAILED DESCRIPTION OF THE INVENTION
  • The invention uses biomass liquids such as sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids mixed with coal or other combustible solids to create alternative fuels. The sugar solutions, vegetable oils, animal fats, triglycerides, methyl esters, glycerin and fatty acids described herein are “green”, i.e. non-hazardous, non-toxic, biodegradable, environmentally friendly, and/or derived from renewable sources.
  • “Combustible solids” means any solid combustible material which can be mixed with one or more biomass liquids as described herein to prepare the alternative fuel of the invention. In an embodiment, the combustible solid is selected from coal, wood chips, coke, and garbage. In another embodiment, the combustible solid is coal. “Coal” includes fine coal from stockpiles, fine coal from impoundments, run of mine coal washed, run of mine coal unwashed and waste coal. Coke is derived from coal. Garbage includes municipal and/or industrial garbage.
  • “Sugar solutions” refers to by-products of sugar beet or sugar cane processing which can comprise one or more components selected from raffinose, glutamine, betaine, lactate, glucose and/or fructose. Other components can include sodium, potassium, chloride, nitrate, nitrite, acetate, ammonia and magnesium. The by-products are also commonly referred to as “de-sugared” solutions.
  • “Black liquor” refers to the liquor resulting from the sulfate or kraft paper processes. Black liquor comprises lignin and tall oil.
  • “Tall oil” refers to a mixture of rosin acids, fatty acids including oleic and linoleic acids and other organic material including sterols and long chain alcohols resulting from acid treatment of black liquor as described above.
  • “Triglycerides” refers to esters of glycerol, a trihydric alcohol, with different fatty acids of varying molecular weight associated with a particular fat or oil. Triglycerides are the principal components of animal fats and vegetable oils. The most common fatty acids sourced from natural fats and oils include palmitic, stearic and linoleic acid.
  • “Fatty acids” means carboxylic acids derived from or contained in an animal or vegetable fat or oil. Fatty acids comprise a terminal COOH group and a long chain saturated or unsaturated alkyl chain. Representative fatty acids include butyric acid, lauric acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, and the like.
  • “Glycerin” and “glycerol” means 1,2,3-propanetriol.
  • Glycerin and fatty acids can be derived as by-products from transesterification reactions involving triglycerides including transesterification reactions involving biodiesel manufacturing processes as described herein.
  • “Methyl esters” and “ethyl esters” means methyl and ethyl esters of fatty acids as described herein.
  • “Vegetable oil” means triglycerides extracted from the seeds, fruit or leaves of plants including corn oil, soybean oil, canola oil, palm oil, coconut oil, rapeseed oil, and the like.
  • In an embodiment, methyl esters, ethyl esters, glycerin and fatty acids are derived from transesterification reactions involving triglycerides.
  • “Transesterification reactions involving triglycerides” refers to the splitting of triglyceride esters derived from vegetable oils and/or animal fats in the presence of base and a monohydroxy alcohol such as methanol or ethanol to produce monoesters of the fatty acids comprising the original triglycerides.
  • Representative fats and oils used in the transesterification reactions described herein include tallow, crude tall oil, virgin vegetable oils, soy, mustard, canola, coconut, rapeseed, palm, poultry offal, fish oils, used cooking oils, and/or trap grease, and the like.
  • In an embodiment, the glycerin, fatty acids, ethyl esters and methyl esters are derived from a biodiesel manufacturing process.
  • Biodiesel is a cleaner-burning diesel replacement fuel made from natural, renewable sources. For example, biodiesel can include fatty acid alkyl esters used as a cleaner-burning diesel replacement fuel made from sources such as new and used vegetable oils and animal fats.
  • According to the American Fuel Data Center of the U.S. Department of Energy, approximately 55% of the biodiesel is currently produced from recycled fat or oil feedstock, including recycled cooking grease. The other half of the industry is limited to vegetable oils, the least expensive of which is soy oil. The soy industry has been the driving force behind biodiesel commercialization because of excess production capacity, product surpluses, and declining prices. Similar issues apply to the recycled grease and animal fats industry, even though these feedstocks are less expensive than soy oils. Based on the combined resources of both industries, there is enough of the feedstock to supply 1.9 billion gallons of biodiesel.
  • Biodiesel is typically made through a chemical process called transesterification in which vegetable oil or animal fats are converted to fatty acid alkyl esters and glycerin by-products. Fatty acids and fatty acid alkyl esters can be produced from oils and fats by base-catalyzed transesterification of the oil, direct acid-catalyzed esterification of the oil and conversion of the oil to fatty acids and subsequent esterification to biodiesel.
  • The majority of fatty acid alkyl esters are produced by the base-catalyzed method. In general, any base may be used as the catalyst used for transesterification of the oil to produce biodiesel, however sodium hydroxide or potassium hydroxide are used in most commercial processes.
  • In the biodiesel manufacturing process, the oils and fats can be filtered and preprocessed to remove water and contaminants. If free fatty acids are present, they can be removed or transformed into biodiesel using special pretreatment technologies, such as acid catalyzed esterification. The pretreated oils and fats can then be mixed with an alcohol and a catalyst (e.g. base). The base used for the reaction is typically sodium hydroxide or potassium hydroxide, being dissolved in the alcohol used (typically ethanol or methanol) to form the corresponding alkoxide, with standard agitation or mixing. It should be appreciated that any suitable base can be used. The alkoxide may then be charged into a closed reaction vessel and the oils and fats are added. The system can then be closed, and held at about 71° C. (160° F.) for a period of about 1 to 8 hours, although some systems recommend that the reactions take place at room temperature.
  • Once the reactions are complete the oil molecules (e.g. triglycerides) are hydrolyzed and two major products are produced: 1) a crude fatty acid alkyl esters phase (i.e. biodiesel phase) and 2) a glycerin by-product phase. Typically, the crude fatty acid alkyl esters phase forms a layer on top of the denser glycerin by-product phase. Because the glycerin by-product phase is denser than the biodiesel phase, the two can be gravity separated. For example, the glycerin by-product phase can be simply drawn off the bottom of a settling vessel. In some cases, a centrifuge may be employed to speed the separation of the two phases.
  • The glycerin by-product phase typically consists of a mixture of glycerin, methyl esters, methanol, mong and inorganic salts and water. Mong is “matiere organique non glycerol”. Mong normally consists of soaps, free fatty acids, and other impurities. Methyl esters are typically present in an amount of about 0.01 to about 5 percent by weight.
  • Methanol can be present in the glycerin and fatty acids in an amount greater than about 5 weight percent to about 30 weight percent. The methanol can be a valuable component in the alternative fuels because of its low flash point which can help ignite the fuel.
  • In certain instances, it may be necessary to further refine the glycerin by-product prior to use, for example by washing, acidulation or distillation to adjust the glycerin concentration and/or remove impurities. Methanol may also be added to the desired concentration.
  • In an embodiment, the glycerin-containing by-product comprises about 30 to about 95 weight percent of glycerin.
  • In an embodiment, the combustible solid is coal and the liquid hydrocarbon component is by-product glycerin.
  • The fatty acid by-products can originate from the refining of the crude fatty acid alkyl esters phase and/or the crude glycerin phase during the biodiesel manufacturing process. For example, the crude fatty acid alkyl esters phase typically includes a mixture of fatty acid alkyl esters, water and a fatty acid salts component. These fatty acid salts component generally form a solution with the water phase (e.g. soap water) where they can be further separated from the fatty acid alkyl esters component. Once separated from the fatty acid alkyl esters component, any suitable acid such as, for example, hydrochloric acid can be added to the water phase containing the fatty acid salts component to produce the fatty acid by-products of the present invention.
  • The fatty acid by-product may be in a wax or solid form. It can also contain fatty acid esters. The esters are beneficial components in the alternative fuel mixture.
  • Similarly, the crude glycerin phase typically includes a mixture of glycerin, water and a fatty acid salts component. This fatty acid salts component forms a solution or suspension with the water phase where it can be further separated from the glycerin component by adding any suitable acid to recover the fatty acid by-products suitable for the present invention.
  • It should be appreciated that the fatty acid by-products of the present invention can be derived from the acidulation of any of the biodiesel manufacturing process streams/stages that contain the fatty acid salts component (e.g. soap water) including, for example, the wash water. These fatty acid by-products derived from any of the different stages/streams of the biodiesel manufacturing process can be used as a component in alternative fuel.
  • The alternative fuels are prepared by applying the desired amount of liquid hydrocarbon component to the combustible solid, for example by spraying onto piles of the combustible solid or by means of showers oriented over conveyors used to transport the combustible solid. If desired, the liquid hydrocarbon component-combustible solid mixture may be mixed to ensure even distribution of the liquid hydrocarbon in the combustible solid.
  • In the case of loose or finely divided combustible solids, the alternative fuel may be prepared by applying the liquid hydrocarbon component to the combustible solid and pressing the resulting material into briquettes or ingots.
  • In an embodiment, about 0.1 to about 49 weight percent of said liquid hydrocarbon component is applied to the combustible solid.
  • In an embodiment, about 0.1 to about 25 weight percent of said liquid hydrocarbon component is applied to the combustible solid.
  • The alternative fuel of this invention may be used as a substitute for, or additive to conventional combustible solids for combustion in boilers or furnaces.
  • Changes can be made in the composition, operation, and arrangement of the method of the invention described herein without departing from the concept and scope of the invention as defined in the claims.

Claims (18)

1. A alternative fuel comprising one or more combustible solids and one or more liquid hydrocarbon components selected from a group consisting of sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids, provided that when the liquid hydrocarbon component is vegetable oil, the combustible solid is other than a cellulosic powder and further provided that when the combustible solid is coal, the liquid hydrocarbon component is other than sugar solutions.
2. The alternative fuel of claim 1 comprising about 0.1 to about 49 weight percent of said liquid hydrocarbon components.
3. The alternative fuel of claim 2 wherein the combustible solid is selected from coal, wood chips, coke and garbage.
4. The alternative fuel of claim 3 comprising about 0.1 to about 25 weight percent of said liquid hydrocarbon components.
5. The alternative fuel of claim 3 wherein the methyl esters, ethyl esters, glycerin and fatty acids are derived from transesterification reactions involving triglycerides.
6. The alternative fuel of claim 3 wherein the methyl esters, ethyl esters, glycerin and fatty acids are derived from a biodiesel manufacturing process.
7. The alternative fuel of claim 3 wherein the combustible solid is coal.
8. The alternative fuel of claim 3 wherein the liquid hydrocarbon is a glycerin-containing by-product of the biodiesel process comprising greater than about 5 to about 30 weight percent methanol.
9. The alternative fuel of claim 8 wherein the glycerin-containing by-product comprises about 30 to about 95 weight percent of glycerin.
10. A method of preparing a alternative fuel comprising applying one or more liquid hydrocarbon components selected from a group consisting of sugar solutions, tall oil, black liquor, vegetable oils, animal fats, triglycerides, methyl esters, ethyl esters, glycerin and fatty acids to one or more combustible solids, provided that when the liquid hydrocarbon component is vegetable oil, the combustible solid is other than a cellulosic powder and further provided that when the combustible solid is coal, the liquid hydrocarbon component is other than sugar solutions.
11. The method of claim 10 wherein about 0.1 to about 49 weight percent of said liquid hydrocarbon components is applied to said combustible solids.
12. The method of claim 11 wherein the combustible solids are selected from coal, wood chips, coke and garbage.
13. The method of claim 12 wherein about 0.1 to about 25 weight percent of said liquid hydrocarbon components are applied to said combustible solids.
14. The method of claim 11 wherein the methyl esters, ethyl esters, glycerin and fatty acids are derived from transesterification reactions involving triglycerides.
15. The method of claim 11 wherein the methyl esters, ethyl esters, glycerin and fatty acids are derived from a biodiesel manufacturing process.
16. The method of claim 11 wherein the combustible solid is coal.
17. The method of claim 16 wherein the liquid hydrocarbon is a glycerin-containing by-product of the biodiesel process comprising greater than about 5 to about 30 weight percent methanol.
18. The method of claim 17 wherein the glycerin-containing by-product comprises about 30 to about 95 weight percent of glycerin.
US11/561,150 2004-05-14 2006-11-17 Alternative fuel comprising combustible solids and by-products or waste material from industrial processes Abandoned US20080115409A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US11/561,150 US20080115409A1 (en) 2006-11-17 2006-11-17 Alternative fuel comprising combustible solids and by-products or waste material from industrial processes
US11/857,093 US20080005956A1 (en) 2004-05-14 2007-09-18 Methods and compositions for controlling bulk density of coking coal
US12/246,975 US20090025276A1 (en) 2006-11-17 2008-10-07 Alternative fuel comprising solids and by_products or waste material from industrial processes
US12/356,352 US20090127499A1 (en) 2004-05-14 2009-01-20 Methods and compositions for dust control and freeze conditioning

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11/561,150 US20080115409A1 (en) 2006-11-17 2006-11-17 Alternative fuel comprising combustible solids and by-products or waste material from industrial processes

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US11/490,193 Continuation-In-Part US7398935B2 (en) 2004-05-14 2006-07-20 Methods and compositions for dust control and freeze control

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US11/857,093 Continuation-In-Part US20080005956A1 (en) 2004-05-14 2007-09-18 Methods and compositions for controlling bulk density of coking coal
US12/246,975 Continuation-In-Part US20090025276A1 (en) 2006-11-17 2008-10-07 Alternative fuel comprising solids and by_products or waste material from industrial processes

Publications (1)

Publication Number Publication Date
US20080115409A1 true US20080115409A1 (en) 2008-05-22

Family

ID=39415517

Family Applications (1)

Application Number Title Priority Date Filing Date
US11/561,150 Abandoned US20080115409A1 (en) 2004-05-14 2006-11-17 Alternative fuel comprising combustible solids and by-products or waste material from industrial processes

Country Status (1)

Country Link
US (1) US20080115409A1 (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080005956A1 (en) * 2004-05-14 2008-01-10 Tran Bo L Methods and compositions for controlling bulk density of coking coal
US20080230487A1 (en) * 2007-03-20 2008-09-25 Malhotra Oil Company Chemical process
WO2009006661A1 (en) * 2007-07-12 2009-01-15 Woelfer Josef Solid fuel comprising a vegetable material and glycerol
US20090025276A1 (en) * 2006-11-17 2009-01-29 Tran Bo L Alternative fuel comprising solids and by_products or waste material from industrial processes
US20090127499A1 (en) * 2004-05-14 2009-05-21 Tran Bo L Methods and compositions for dust control and freeze conditioning
FR2934032A1 (en) * 2008-07-15 2010-01-22 Le Clerc De Bussy Jacques Mari Wetwood i.e. green wood, combusting method for use in furnace, involves heating wetwood for disengaging water vapor and pyroligneous content, where content is subjected to cracking for complete combustion of combustible gas
WO2010020393A1 (en) * 2008-08-18 2010-02-25 Loehr Tobias Fuel system and method for producing the same
US20110088751A1 (en) * 2008-06-30 2011-04-21 James Rosa Non-imaging radiant energy concentrator
US8955685B2 (en) 2010-12-30 2015-02-17 Nalco Company Glycerides and fatty acid mixtures and methods of using same
US9796896B2 (en) 2011-12-21 2017-10-24 Joan Lynch Fertilizer and fertilizer additive compositions and methods comprising by-products from the manufacture of fatty acid alkyl esters and/or biodiesel

Citations (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2578816A (en) * 1949-03-07 1951-12-18 Swift & Co Glycerin refining
US4417992A (en) * 1981-07-30 1983-11-29 Nalco Chemical Company Dust control
US4426409A (en) * 1982-07-02 1984-01-17 Nalco Chemical Company Cationic polymers for use in freeze protection of coals and minerals
US4594268A (en) * 1985-03-29 1986-06-10 Calgon Corporation Method for the control of dust using methacrylate containing emulsions and compositions
US4689251A (en) * 1986-01-29 1987-08-25 Desoto, Inc. Anticaking and antidusting composition
US5104711A (en) * 1989-11-17 1992-04-14 Marsek Patrick W Liquid spray masking system and method
US5194174A (en) * 1990-06-18 1993-03-16 Betz Laboratories, Inc. Methods for suppressing fugitive dust emissions
US5244472A (en) * 1987-05-13 1993-09-14 Simmons John J Preparation of chemically dried cellulosic fuel
US5421835A (en) * 1993-11-29 1995-06-06 Harding; Blake W. Spontaneously ignitable fire starter composition
US5431702A (en) * 1993-03-25 1995-07-11 Dynecology, Inc. Waste conversion process and products
US5439608A (en) * 1993-07-12 1995-08-08 Kondrats; Nicholas Methods for the collection and immobilization of dust
US5858032A (en) * 1994-11-02 1999-01-12 Advanced Natural Fuels Limited Solid fuels
US20010023653A1 (en) * 1998-12-10 2001-09-27 3M Innovative Properties Company Low dust wall repair compound
US20010042340A1 (en) * 2000-02-17 2001-11-22 Tatsuo Tateno Process for producing fatty acid esters and fuels comprising fatty acid ester
US6399802B2 (en) * 2000-03-24 2002-06-04 Kru Feed Energy Company Method for soapstock acidulation
US6491736B1 (en) * 2001-04-30 2002-12-10 Montana Sulphur & Chemical Company Polyhydric alcohol anti-dust agent for inorganic materials
US6589442B1 (en) * 2000-08-08 2003-07-08 Q-X Enviro Products Ltd. Dust control composition
US20040159042A1 (en) * 2003-02-06 2004-08-19 Murcia Philippe R. Organically clean biomass fuel
US20050000150A1 (en) * 2003-07-02 2005-01-06 The Procter & Gamble Company Method for combustion of pulverized coal with reduced emissions
US6878308B2 (en) * 2001-12-28 2005-04-12 Grain Processing Corp. Method for inhibiting freeze-clumping of aggregate materials
US20050087720A1 (en) * 2002-10-28 2005-04-28 Samuels William D. Deicing/anti-icing fluids
US6890451B2 (en) * 2003-09-23 2005-05-10 Richard Sapienza Environmentally benign anti-icing or deicing fluids employing triglyceride processing by-products
US20050142250A1 (en) * 2002-06-03 2005-06-30 Agb, Llc Method of processing waste product into fuel
US7108800B2 (en) * 2004-05-14 2006-09-19 Nalco Company Method for preventing the agglomeration or generation of dust from a particulate material comprising coal
US7147679B2 (en) * 2000-08-30 2006-12-12 William Tis Synthetic fuel production method
US20060284137A1 (en) * 2004-05-14 2006-12-21 Tran Bo L Methods and compositions for dust control and freeze control
US20070113465A1 (en) * 2005-11-21 2007-05-24 Pech Craig W Method for manufacture and use of the waste stream from biodiesel production (crude glycerin) as a commercial fuel

Patent Citations (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2578816A (en) * 1949-03-07 1951-12-18 Swift & Co Glycerin refining
US4417992A (en) * 1981-07-30 1983-11-29 Nalco Chemical Company Dust control
US4426409A (en) * 1982-07-02 1984-01-17 Nalco Chemical Company Cationic polymers for use in freeze protection of coals and minerals
US4594268A (en) * 1985-03-29 1986-06-10 Calgon Corporation Method for the control of dust using methacrylate containing emulsions and compositions
US4689251A (en) * 1986-01-29 1987-08-25 Desoto, Inc. Anticaking and antidusting composition
US5244472A (en) * 1987-05-13 1993-09-14 Simmons John J Preparation of chemically dried cellulosic fuel
US5104711A (en) * 1989-11-17 1992-04-14 Marsek Patrick W Liquid spray masking system and method
US5194174A (en) * 1990-06-18 1993-03-16 Betz Laboratories, Inc. Methods for suppressing fugitive dust emissions
US5431702A (en) * 1993-03-25 1995-07-11 Dynecology, Inc. Waste conversion process and products
US5439608A (en) * 1993-07-12 1995-08-08 Kondrats; Nicholas Methods for the collection and immobilization of dust
US5421835A (en) * 1993-11-29 1995-06-06 Harding; Blake W. Spontaneously ignitable fire starter composition
US5858032A (en) * 1994-11-02 1999-01-12 Advanced Natural Fuels Limited Solid fuels
US20010023653A1 (en) * 1998-12-10 2001-09-27 3M Innovative Properties Company Low dust wall repair compound
US20010042340A1 (en) * 2000-02-17 2001-11-22 Tatsuo Tateno Process for producing fatty acid esters and fuels comprising fatty acid ester
US6399802B2 (en) * 2000-03-24 2002-06-04 Kru Feed Energy Company Method for soapstock acidulation
US6589442B1 (en) * 2000-08-08 2003-07-08 Q-X Enviro Products Ltd. Dust control composition
US7147679B2 (en) * 2000-08-30 2006-12-12 William Tis Synthetic fuel production method
US20020184933A1 (en) * 2001-04-30 2002-12-12 Montana Sulphur & Chemical Company Polyhydric alcohol anti-dust agent for inorganic materials
US6491736B1 (en) * 2001-04-30 2002-12-10 Montana Sulphur & Chemical Company Polyhydric alcohol anti-dust agent for inorganic materials
US6878308B2 (en) * 2001-12-28 2005-04-12 Grain Processing Corp. Method for inhibiting freeze-clumping of aggregate materials
US20050142250A1 (en) * 2002-06-03 2005-06-30 Agb, Llc Method of processing waste product into fuel
US20050087720A1 (en) * 2002-10-28 2005-04-28 Samuels William D. Deicing/anti-icing fluids
US6818027B2 (en) * 2003-02-06 2004-11-16 Ecoem, L.L.C. Organically clean biomass fuel
US20040159042A1 (en) * 2003-02-06 2004-08-19 Murcia Philippe R. Organically clean biomass fuel
US20050000150A1 (en) * 2003-07-02 2005-01-06 The Procter & Gamble Company Method for combustion of pulverized coal with reduced emissions
US6890451B2 (en) * 2003-09-23 2005-05-10 Richard Sapienza Environmentally benign anti-icing or deicing fluids employing triglyceride processing by-products
US7108800B2 (en) * 2004-05-14 2006-09-19 Nalco Company Method for preventing the agglomeration or generation of dust from a particulate material comprising coal
US20060284137A1 (en) * 2004-05-14 2006-12-21 Tran Bo L Methods and compositions for dust control and freeze control
US20070113465A1 (en) * 2005-11-21 2007-05-24 Pech Craig W Method for manufacture and use of the waste stream from biodiesel production (crude glycerin) as a commercial fuel

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080005956A1 (en) * 2004-05-14 2008-01-10 Tran Bo L Methods and compositions for controlling bulk density of coking coal
US20090127499A1 (en) * 2004-05-14 2009-05-21 Tran Bo L Methods and compositions for dust control and freeze conditioning
US20090025276A1 (en) * 2006-11-17 2009-01-29 Tran Bo L Alternative fuel comprising solids and by_products or waste material from industrial processes
US20080230487A1 (en) * 2007-03-20 2008-09-25 Malhotra Oil Company Chemical process
WO2009006661A1 (en) * 2007-07-12 2009-01-15 Woelfer Josef Solid fuel comprising a vegetable material and glycerol
US20110088751A1 (en) * 2008-06-30 2011-04-21 James Rosa Non-imaging radiant energy concentrator
FR2934032A1 (en) * 2008-07-15 2010-01-22 Le Clerc De Bussy Jacques Mari Wetwood i.e. green wood, combusting method for use in furnace, involves heating wetwood for disengaging water vapor and pyroligneous content, where content is subjected to cracking for complete combustion of combustible gas
WO2010020393A1 (en) * 2008-08-18 2010-02-25 Loehr Tobias Fuel system and method for producing the same
EP2177593A1 (en) * 2008-08-18 2010-04-21 Tobias Löhr Fuel system and method for manufacturing the same
WO2010042590A1 (en) * 2008-10-07 2010-04-15 Nalco Company Alternative fuel comprising solids and by-products or waste material from industrial processes
US8955685B2 (en) 2010-12-30 2015-02-17 Nalco Company Glycerides and fatty acid mixtures and methods of using same
US10384958B2 (en) 2010-12-30 2019-08-20 Ecolab Usa Inc. Glycerides and fatty acid mixtures and methods of using same
US9796896B2 (en) 2011-12-21 2017-10-24 Joan Lynch Fertilizer and fertilizer additive compositions and methods comprising by-products from the manufacture of fatty acid alkyl esters and/or biodiesel

Similar Documents

Publication Publication Date Title
US20080115409A1 (en) Alternative fuel comprising combustible solids and by-products or waste material from industrial processes
Karmakar et al. Progress and future of biodiesel synthesis: Advancements in oil extraction and conversion technologies
Bora et al. Sewage sludge to bio-fuel: A review on the sustainable approach of transforming sewage waste to alternative fuel
Chakraborty et al. Conversion of slaughterhouse and poultry farm animal fats and wastes to biodiesel: Parametric sensitivity and fuel quality assessment
Esmaeili A critical review on the economic aspects and life cycle assessment of biodiesel production using heterogeneous nanocatalysts
BODDULA Microwaves in organic synthesis
Atabani et al. A comprehensive review on biodiesel as an alternative energy resource and its characteristics
Kralova et al. Biofuels–renewable energy sources: a review
Enweremadu et al. Technical aspects of production and analysis of biodiesel from used cooking oil—A review
Haas et al. 2 Alternate Feedstocks and Technologies for Biodiesel Production
Balat et al. Progress in biodiesel processing
Izah et al. The challenge of biodiesel production from oil palm feedstock in Nigeria
RU2503714C2 (en) Integrated method of producing biofuel from different types of raw material and related products
Hidawati et al. Treatment of glycerin pitch from biodiesel production
Lee et al. Prospects for biodiesel as a byproduct of wood pulping–a review
US20090025276A1 (en) Alternative fuel comprising solids and by_products or waste material from industrial processes
Ilham Biomass classification and characterization for conversion to biofuels
Sidohounde et al. Transesterification reaction and comparative study of the fuel properties of biodiesels produced from vegetable oils: a review
Sarma et al. Recent inventions in biodiesel production and processing-A review
Panneerselvam et al. Biodiesel production from mutton tallow
Kattimani et al. Technologies for biodiesel production from non-edible oils: A review
Baloch et al. Application of microwave synthesis in biodiesel production
Patel et al. In-depth analysis of waste cooking oil as renewable and ecofriendly biofuel candidate
Yunus et al. Oil Palm as bioenergy feedstock
Sulistyo et al. Crude candlenut oil ethanolysis to produce renewable energy at ambient condition

Legal Events

Date Code Title Description
AS Assignment

Owner name: NALCO COMPANY, ILLINOIS

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:TRAN, BO L.;REEL/FRAME:018869/0629

Effective date: 20070119

AS Assignment

Owner name: BANK OF AMERICA, N.A., AS COLLATERAL AGENT, NEW YO

Free format text: SECURITY AGREEMENT;ASSIGNORS:NALCO COMPANY;CALGON LLC;NALCO ONE SOURCE LLC;AND OTHERS;REEL/FRAME:022703/0001

Effective date: 20090513

Owner name: BANK OF AMERICA, N.A., AS COLLATERAL AGENT,NEW YOR

Free format text: SECURITY AGREEMENT;ASSIGNORS:NALCO COMPANY;CALGON LLC;NALCO ONE SOURCE LLC;AND OTHERS;REEL/FRAME:022703/0001

Effective date: 20090513

AS Assignment

Owner name: NALCO COMPANY, ILLINOIS

Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:BANK OF AMERICA, N.A.;REEL/FRAME:035771/0668

Effective date: 20111201

AS Assignment

Owner name: NALCO COMPANY, ILLINOIS

Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:BANK OF AMERICA, N.A.;REEL/FRAME:041808/0713

Effective date: 20111201

AS Assignment

Owner name: ECOLAB USA INC., MINNESOTA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:NALCO COMPANY LLC;CALGON CORPORATION;CALGON LLC;AND OTHERS;REEL/FRAME:041836/0437

Effective date: 20170227

Owner name: NALCO COMPANY LLC, DELAWARE

Free format text: CHANGE OF NAME;ASSIGNOR:NALCO COMPANY;REEL/FRAME:041835/0903

Effective date: 20151229

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION

AS Assignment

Owner name: ECOLAB USA INC., MINNESOTA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:NALCO COMPANY;REEL/FRAME:042147/0420

Effective date: 20170227