CA2629121A1 - Processes of producing biodiesel and biodiesel produced therefrom - Google Patents

Processes of producing biodiesel and biodiesel produced therefrom Download PDF

Info

Publication number
CA2629121A1
CA2629121A1 CA002629121A CA2629121A CA2629121A1 CA 2629121 A1 CA2629121 A1 CA 2629121A1 CA 002629121 A CA002629121 A CA 002629121A CA 2629121 A CA2629121 A CA 2629121A CA 2629121 A1 CA2629121 A1 CA 2629121A1
Authority
CA
Canada
Prior art keywords
biodiesel
oil
filter
steryl glycosides
compound capable
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
CA002629121A
Other languages
French (fr)
Inventor
Inmok Lee
Lisa Pfalzgraf
Leif Solheim
Scott Bloomer
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.)
Archer Daniels Midland Co
Original Assignee
Archer-Daniels-Midland Company
Inmok Lee
Lisa Pfalzgraf
Leif Solheim
Scott Bloomer
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 Archer-Daniels-Midland Company, Inmok Lee, Lisa Pfalzgraf, Leif Solheim, Scott Bloomer filed Critical Archer-Daniels-Midland Company
Publication of CA2629121A1 publication Critical patent/CA2629121A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • C11C3/003Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fatty acids with alcohols
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/48Separation; Purification; Stabilisation; Use of additives
    • C07C67/56Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/48Separation; Purification; Stabilisation; Use of additives
    • C07C67/58Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
    • 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
    • C10L1/02Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • C10L1/026Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for compression ignition
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C1/00Preparation of fatty acids from fats, fatty oils, or waxes; Refining the fatty acids
    • C11C1/08Refining
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/10Feedstock materials
    • C10G2300/1011Biomass
    • 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
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P30/00Technologies relating to oil refining and petrochemical industry
    • Y02P30/20Technologies relating to oil refining and petrochemical industry using bio-feedstock

Abstract

The present disclosure concerns a process for removing steryl glycosides or monoacylglycerols from biodiesel by contact of the biodiesel with an absorbant, or filter aid. Treated biodiesel as well as steryl glycosides derived from biodiesel are also disclosed.

Description

PROCESSES OF PRODUCING BIODIESEL
AND BIODIESEL PRODUCED THEREFROM

TECHNICAL FIELD
The present disclosure relates generally to biodiesel and processes for producing biodiesel.
BACKGROUND
Biodiesel is manufactured from animal or vegetable oils. The preferred feedstock for producing biodiesel in Europe is rapeseed (i.e., canola) oil. !n North America, some canola oil is used to produce biodiesel, but soybean oil is also used as a feedstock in producing biodiesel. Biodiesel is used as an additive to petroleum-derived diesel fuel or as a substitute for petroleum-derived diesel fuel in diesel (compression-ignition) engines. Biodiesel usually comprises fatty acid methyl esters (FAME) or fatty acid ethyl esters.
The use of biodiesel in cold climates may require special considerations due to the tendency of precipitates to form in the biodiesel at temperatures of 0 C and below. These precipitates impair the flow characteristics of biodiesel.

SUMMARY OF THE INVENTION
The present invention discloses processes for producing biodiesel as well as biodiesel produced therefrom.
In one embodiment, a process for treating biodiesel comprises placing biodiesel in contact with a compound capable of removing steryl glycosides from the biodiesel.

In another embodiment, a process for treating biodiesel comprises placing biodiesel in contact with a compound capable of removing monoacylglycerols from the biodiesel.
In another embodiment, a process for treating biodiesel comprises reducing the filter blocking tendency of the biodiesel.
In another embodiment, a process for removing steryl glycosides from a fatty acid methyl ester containing material comprises placing a compound selected from the group consisting of adsorbents, filter aids, boric acid, soap, sucrose, sugar, glucose, carbon, activated carbon, cellulose, sodium chloride, citric acid, magnesium silicate, clay, diatomaceous earth, lecithin, granular clay, granular glucose, granular sugar, protein, textured vegetable protein, solutions of boric acid, silica hydrogel, and combinations of any thereof in contact with a fatty acid containing material, and separating the compound from the fatty acid containing material.
In another embodiment, a process for removing monoacylglycerols from a fatty acid methyl ester containing material or biodiesel comprises placing a compound selected from the group consisting of magnesium silicate, steryl glycosides, and a combination thereof in contact with the fatty acid methyl ester containing material or the biodiesel.
In another embodiment, the biodiesel is separated from the compounds capable of removing monoacylglycerols from the biodiesel. In an embodiment, the compound is separated from the fatty acid containing material by a process selected from the group consisting of filtration, centrifugation, and combinations of any thereof.
In another embodiment, the biodiesel separated from the compounds capable of removing monoacylglycerols from the biodiesel is mixed with a petroleum based diesel fuel, a biodiesel not placed in contact with the compound capable of removing the monoacylglycerols, ethanol, or any combinations thereof.
In an additional embodiment, a process for reducing the filter blocking tendency of biodiesel includes placing the biodiesel in contact with a solid or liquid, wherein the solid or liquid comprises a compound capable of reducing the filter blocking tendency of biodiesel.
In yet a further embodiment, a process for producing biodiesel includes mixing a fatty acid containing material and an alcohol, thus producing a biodiesel precursor mixture. The biodiesel precursor mixture is subjected to a condition that allows biodiesel to form, wherein the condition is selected from the group consisting of time, an increased temperature, an increased pressure, the presence of a catalyst, and any combination thereof. The process further includes isolating the biodiesel and removing steryl glycosides from the biodiesel, wherein the steryl glycosides are removed from the biodiesel at a temperature of less than 125 C.
In yet 'a further embodiment, a process for producing biodiesel includes mixing a fatty acid containing material and an alcohol, thus producing a biodiesel precursor mixture. The biodiesel precursor mixture is subjected to a condition that allows biodiesel to form, wherein the condition is selected from the group consisting of time, an increased temperature, an increased pressure, the presence of a catalyst, and any combination thereof. The process further includes isolating the biodiesel and removing monoacylglycerols from the biodiesel, wherein the monoacyiglycerols are removed from the biodiesel at a temperature of less than 125 C. In an embodiment, the biodiesel is of soy origin.
In yet another embodiment, a biodiesel production plant comprises a compound capable of removing steryl glycosides from the biodiesel, and a conduit operably configured to place biodiesel in contact with the compound capable of removing steryl glycosides from the biodiesel.
In yet another embodiment, a biodiesel production plant comprises a compound capable of removing monoacylglycerols from the biodiesel, and a conduit operably configured to place biodiesel in contact with the compound capable of removing steryl monoacylglycerols from the biodiesel.
In another embodiment, an apparatus configured to treat biodiesel includes a reservoir for containing a biodiesel having an initial filter blocking tendency value, a compound capable of removing steryl glycosides from the biodiesel, and a conduit operatively configured to place the biodiesel in contact with the compound capable of removing steryl glycosides from the biodiesel.
In another embodiment, an apparatus configured to treat biodiesel includes a reservoir for containing a biodiesel having an initial filter blocking tendency value, a compound capable of removing monoacylglycerols from the biodiesel, and a conduit operatively configured to place the biodiesel in contact with the compound capable of removing monoacylglycerols from the biodiesel.
In a further embodiment, a process for preparing a composition enriched in steryt glycosides includes filtering a steryl glycoside containing composition through a bed of water-soluble solid bed material, and dissolving the water-soluble solid bed material in water to remove the water-soluble solid bed material, wherein a composition enriched in steryl glycosides is obtained.
In one embodiment, a steryl glycoside composition comprising steryl glycosides or a biodiesel origin is disclosed.
In a further embodiment, a biodiesel includes a detectable level of steryl glycosides, wherein a level of steryl glycosides in the biodiesel is less than 70 ppm.
In still a further embodiment, a biodiesel comprises a detectable level of steryl glycosides, rnonoacylglycerols, diacylgiycerols, triacylglycerols, or any combinations thereof, wherein the biodiesel passes a filter blocking test.
The filter blocking test includes determining whether a pre-selected volume of the product passes through a filter before a pre-selected pressure is placed on the filter from the product. When the pre-selected volume of the product passes through the filter before the pre-selected pressure is reached, the biodiesel passes the filter blocking test. When the pre-selected pressure is reached before the pre-selected volume of the product passes through the filter, the biodiesel fails the filter blocking test.
In another embodiment, a biodiesel comprises a detectable level of steryl glycosides, monoacylglycerols, diacylglycerols, triacylglycerols, or any combination thereof, and passes a filter blocking test. The filter blocking test comprises: adjusting a temperature of a sample of the biodiesel to 15 to 25 degrees Celsius; shaking the sample for 120 seconds; allowing the sample to stand on a vibration-free surface for 300 seconds; placing 320 milliliters of the sample into a fuel reservoir beaker of a Normalab Analis NBF 240 instrument;
ensuring that the temperature of the sample is maintained at the 15 to 25 degrees Celsius; placing a pump suction pipe of the Normalab Analis NBF 240 instrument into the fuel reservoir beaker; operating a pump of the Normalab Analis NBF 240 instrument until biodiesel flows into a collection beaker;
pouring any fuel from the collection beaker into the fuel reservoir beaker; placing a fresh filter on a filter unit of the Normalab Analis NBF 240 instrument; attaching the assembled filter unit to the Normalab Analis NBF 240 instrument with a Luer fitting; starting the pump of the Normalab Analis NBF 240 instrument; reading a pressure gauge after 20 seconds; and pumping the sample at a flow rate of 20 ml/minute until 300 milliliters have passed through the filter or until the pressure gauge reaches 105 kPa. The biodiesel passes the filter blocking test when 300 milliliters of the sample passes through the filter before 105 kPa is reached, and fails the filter blocking test when 105 kPa is reached before 300 milliliters of the sample passes through the sample.
In another embodiment, a biodiesel comprises a detectable level of steryl glycosides, monoacylglycerols, diacylglycerols, triacylglycerols, or combinations of any thereof, and passes a filter blocking test. The filter blocking test comprises: filtering 30 milliliters of biodiesel through a 1.6 um GF/A
fiiter having 47 mm diameter under a 21-25-inch Hg vacuum. The biodiesel passes the filter blocking test when the entire sample of 300 ml passes through the filter in 6 minutes or less.
In a further exemplary embodiment, a process for treating biodiesel comprises placing biodiesel in contact with a compound selected from the group consisting of adsorbents, filter aids, boric acid, soap, sucrose, sugar, glucose, carbon, activated carbon, cellulose, sodium chloride, citric acid, magnesium silicate, clay, diatomaceous earth, lecithin, granular clay, granular glucose, granular sugar, protein, textured vegetable protein, steryl glycosides, and combinations of any thereof, and separating the biodiesel from the compound.
In another embodiment, the fatty acid containing material from which steryl glycosides, monoacylglycerols, or combinations thereof are separated is selected from the group consisting of vegetable oil, canola oil, safflower oil, sunflower oil, nasturtium seed oil, mustard seed oil, olive oil, sesame oil, soybean oil, corn oil, peanut oil, cottonseed oil, rice bran oil, babassu nut oil, castor oil, palm oil, palm kernel oil, rapeseed oil, low erucic acid rapeseed oil, lupin oil, jatropha oil, coconut oil, flaxseed oil, evening primrose oil, jojoba oil, camelina oil, tallow, beef tallow, butter, chicken fat, lard, dairy butterfat, shea butter, biodiesel, used frying oil, oil miscella, used cooking oil, yellow trap grease, hydrogenated oils, derivatives of the oils, fractions of the oils, conjugated derivatives of the oils, and mixtures of any thereof.
In an embodiment, biodiesel is mixed with a solid or liquid capable of improving the cold test results of a biodiesel. In an embodiment, the solid or liquid is mixed with the biodiesel at a first temperature and the solid -or liquid is separated from the biodiesel; the biodiesel is adjusted to have a second temperature, and the biodiesel is subjected to a cold test.
In a further embodiment, biodiesel is incubated at a first temperature, filtered through a compound, incubated at a second temperature, and subjected to a filter blocking test. In a further embodiment, the biodiesel is incubated at 40 F (4 C), filtered through a compound selected from the group consisting of diatomaceous earth and cellulose, incubated at a second temperature, and subjected to a filter blocking test.
DETAILED DESCRIPTION OF THE INVENTION
Biodiesei comprises ethyl or methyl esters of fatty acids of biological origin. Starting materials for the production of biodiesel include, but are not limited to, materials containing fatty acids. These materials include, without limitation, triacylglycerols, diacylglycerols, monoacyiglycerols, phospholipids, esters, free fatty acids, or any combinations thereof. The biodiesel is produced by incubating the material including the fatty acids with a short chain alcohol in the presence of heat, pressure, a catalyst, or combinations of any thereof to produce fatty acid esters of the short chain alcohols. In industrial practice, biodiesel may undergo a final simple filtration step, such as through a polishing "sock" filter, to remove any remaining fine particulate matter. Such a filter step may comprise a first screen having 10 micron pore size and a second screen of 1 micron pore size. These fatty acid esters of the short chain alcohols may be used as supplements to or replacements for diesel fuel in compression ignition engines.
The fatty acids used to produce the biodiesel may originate from a wide variety of natural sources including, but not limited to, vegetable oil, canola oil, safflower oil, sunflower oil, nasturtium seed oil, mustard seed oil, olive oil, sesame oil, soybean oil, corn oil, peanut oil, cottonseed oil, rice bran oil, babassu nut oil, castor oil, palm oil, palm oil, rapeseed oil, low erucic acid rapeseed oil, palm kernel oil, lupin oil, jatropha oil, coconut oil, flaxseed oil, evening primrose oil, jojoba oil, camelina oil, tallow, beef tallow, butter, chicken fat, lard, dairy butterfat, shea butter, biodiesel, used frying oil, oil miscella, used cooking oil, yellow trap grease, hydrogenated oils, derivatives of the oils, fractions of the oils, conjugated derivatives of the oils, and mixtures of any thereof.
Some components of biodiesel such as, for example, esters of saturated fatty acids may cause the development of crystals when the biodiesel is subjected to cold conditions. For instance, the presence of methyl ester containing saturated fatty acids, monoacyiglycerol (monoglyceride) containing saturated fatty acids, diacylglycerol (diglyceride) containing saturated fatty acids (as low as 0.1 wt !o), and unsaponifiable matter (at levels of 3%) may cause cold-flow problems in biodiesel. As one example, monoacylglycerols containing saturated fatty acids may form crystals in the biodiesel and may cause flow problems or fuel blockages in biodiesel fuel systems. In another example, a fuel blockage in a biodiesel fuel system may be caused by the cooling of esters of saturated fatty acids in the biodiesel. These fuel blockages may occur when vehicles powered by biodiesel or a blend of diesel and biodiesel are exposed to cold conditions. These problems caused by the crystals or cooled esters of saturated fatty acids may be rectified by heating and, thus, melting the crystallized materials or heating the cooled esters of saturated fatty acids.
The heat may be applied by towing the affected vehicle to a warm garage, or applying a heat source such as a heat blower to the fuel lines and systems of the vehicle. Under these conditions, fuel flow is restored when the crystallized material melts, and esters of saturated fatty acids pass into the combustion chamber for burning.
The formation of precipitates at temperatures of 0 C and below resulted in the development of tests to measure the impact of cold temperatures on biodiesel. For instance, in the USA, the cloud point of the biodiesel is determined with the ASTM method D2500. In Europe, the cold filter plugging point of biodiesel of heating oil is determined with a test designated EN116.
These tests are used to ensure that the biodiesel falls within the required standards. However, these tests do not account for the presence of precipitates which may form.in soy biodiesel without exposure to cold temperatures. These precipitates can cause fuel blockage such as restriction or blockage of fuel filters, which is distinct from the problem of the precipitation of esters of saturated fatty acids caused by exposure to cold.
In one embodiment, the fatty acid containing materials or products used to produce the biodiesel may also be subjected to processes to separate solid material, such as esters of saturated fatty acids, from liquid material, such as esters of unsaturated fatty acids and polyunsaturated fatty acids to remove the solid material and prevent any potential blocking issues.
Biodiesel has been scrutinized because an amorphous cloud-like substance may develop in the biodiesel when stored at room temperature in addition to the flow problems that occur at cold temperatures. This amorphous cloud-like substance may cause clogging of fuel filters. The resulting constriction or stoppage of fuel flow is not related to cold temperatures and requires the frequent changing of filters, which is costly and inconvenient.
The amorphous cloud-like substance that is observed at room temperature is not crystallized esters of fatty acids, such as saturated methyl esters or mono-, di-, or triacylglycerols of saturated fatty acids.
In another embodiment, it was surprisingly discovered that the amorphous cloud-like substance included steryi glycosides. These steryl glycosides in biodiesel increase the filter blocking tendency of biodiesel without exposure of the biodiesel to cold temperatures.
In a further embodiment, crystals formed in biodiesel at room temperature were observed under the microscope. The crystals appeared as particles of about 10-15 microns in size. The crystals were associated together in loose, amorphous, gel-like agglomerates of various sizes. After incubating biodiesel containing the crystals with water for a few hours, the morphology of the individual particles and the agglomerates changed, indicating the presence of surface-active material. These crystals were recovered and identified as steryl glycosides. The steryl glycosides include sterol glucosides, steryl glucosides, or sterol glycosides.
The steryl glycoside crystals may also contain fatty acid methyl esters (FAME), which may be entrapped or bound. The presence of steryl glycosides in biodiesel can be detected by the development or presence of a visible opacity or "haze" in the biodiesel at room temperature without a microscope. In another embodiment, it was determined that the amount of haze visible in room-temperature biodiesel (--25 C) is related to the tendency of biodiesel to fail a filter blocking test designed to test the flow of fuel at 15-25 C.
The steryl glycosides present in biodiesel comprise a sterol group linked to a carbohydrate at the hydroxyl moiety of the sterol. The steryl glycosides may also contain a fatty acid esterified to a hydroxyl group of the carbohydrate moiety; these compounds may be described as acylated steryl glycosides. It was also found that the ability of the steryl glycosides to increase the filter blocking occurred regardless of the presence of meltable crystals of glycerol esters of saturated fatty acids or the presence of a fatty acid moiety.
Acylated steryl glycosides are naturally occurring compounds found in plants. The acylated steryl glycosides comprise a sterol group bound to a carbohydrate having a fatty acid acylated to the primary hydroxyl group of the carbohydrate moiety of a steryl glycoside. One of the acylated steryl glycosides present in soybean extracts is the 6'-Iinoleoyl-beta-D-glucoside of beta sitosterol present at about 47%. In plants, other fatty acids or monobasic carboxylic acids, such as paimitic acid, oleic acid, stearic acid, linoleic acid, and linolenic acid may also be acylated to the carbohydrate moiety through an ester bond. The acylated steryl glycosides are two to ten times more abundant in plants than the (non-acylated) steryl glycosides. Steryl glycosides, also known as sterolins, are present as monoglycosides in the oil from which biodiesel is synthesized, although a few diglycosides also exist. A common sugar in steryl glycosides is D-glucose, which is joined to the sterol via the 3-beta-hydroxy group by means of an equatorial or beta-glucoside bond. Other monosaccharides that may be found in steryl glycosides include mannose, galactose, arabinose and xylose.
The amount of steryl glycosides in crude soybean oil is higher than in corn oil or sunflower oil. Crude soy oil may contain about 2300 ppm steryl glycosides, while crude oils from corn and sunflower contain about 500 ppm and 300 ppm, respectively. Steryl glycosides are enriched in gums produced by degumming soy, corn and sunflower oils, and present in concentrations of about 19300 ppm, 5400 ppm, and 16800 ppm, respectively, and can be expected to be similarly enriched in soapstock and acid oils from vegetable oils.
In oil refining, gums resulting from degumming crude oil and soapstock resulting from alkali refining of crude oil or degummed oil are often further processed to recover entrained oil and fatty acids. This process may be carried out by hydrolysis of the gums or soapstock to increase the content of free fatty acids. Hydrolysis may be carried out by the application of steam and alkali or acid. Acid is sometimes used because the acid facilitates separation of a free fatty acid phase from a water-rich phase. The free fatty acid phase is a product called "acid oil". Acid oil may be used as a feedstock for biodiesel synthesis. The glycosides in gums and soapstock can also be present in the acid oil, so biodiesel made from acid oil can have high levels of steryl glycosides and result in the flow problems described herein.
The steryl glycosides in the biodiesel cause problems for flow of the biodiesel. Even low levels of the steryl glycosides (i.e., 10-90 ppm) in the biodiesel can form aggregates with fatty acid methyl esters that may appear as a visible cloud. These aggregates can accelerate filter plugging at any temperature, not just cold temperatures, due to the high melting point of steryl glycosides (i.e., 240 C). At room temperatures, the steryl glycosides can aggregate and plug filters used for biodiesel fuel. At cold temperatures, the cold-flow probiems caused by alkyl esters of saturated fatty acids such as monoacylglycerols may be compounded by the presence of the steryl glycosides.
The steryl glycosides not only cause problems for flow of the biodiesel, but can also hamper the production of biodiesel. For instance, since biodiesel is often centrifuged as a final polishing step in the manufacture of biodiesel, the centrifuges used for the final purification step can become filled with steryl glycoside-rich solids, resulting in costly process interruptions and shut-downs to clean the centrifuges. In addition, since biodiesel is often subjected to a final polishing filtration step, such as by passage through a sock filter, the sock filters can become filled or blinded (occluded) with steryl glycoside-rich solids, also resulting in costly process interruptions and shut-downs to clean and/or replace the filter material.
The formation of steryl glycoside crystals in the biodiesel may be exacerbated in the presence of trace amounts of water. This is because the steryl glycosides, visible as haze in biodiesel, may grow in volume when the steryl glycosides are placed in contact with water. The grown or expanded steryl glycoside crystals make the crystals even more prone to causing fuel restriction or blockage.
Unlike esters of saturated fatty acids, steryl glycosides cannot be practically removed by melting or exposure to heat since the melting point of steryl glycosides is 240 C. This means that the steryl glycosides cannot be practically heated and melted to allow the steryl glycosides to pass through a filter into a combustion chamber for burning. Further, in the event= the steryl glycosides were to reach the fuel injectors of a diesel engine, the steryl glycosides may accumulate and form a refractory gum-like material that would require disassembly and cleaning of the injectors, thus increasing the operating expense of the diesel engine.
Further, since the steryl glycosides are insoluble in most solvents, with the exception of pyridine, dioxane and dimethylformamide, the cleaning of components having accumulated steryl glycosides is problematic.
This is because pyridine, dioxane and dimethylformamide are not found in the usual diesel repair facility, and their health hazards make these solvents unsafe for use outside of a fume hood. Consequently, the build-up of the steryl glycosides on diesel engine components would require labor-intense abrasive cleaning or expensive replacement of fuel injectors and other fouled components.
In another embodiment, processes for removing steryl glycosides from biodiesel or oils are disclosed. The steryl glycosides are removed by placing the biodiesel or oil in contact with a compound capable of removing the steryl glycosides from the biodiesel or oil. By removing the steryl glycosides from the biodiesel, the biodiesel has a reduced tendency to have a retarded flow or block filters.
In another embodiment, a biodiesei placed in contact with a compound capable of removing steryl glycosides (i.e., treated biodiesel) has a reduced amount of steryl glycosides as compared to a biodiesel not placed in contact with a compound capable of removing steryl glycosides (i.e., untreated biodiesel). The treated biodiesel also has a reduced filter blocking tendency as compared to the untreated biodiesel. The treated biodiesel may have a FBT
value of less than 1.414 as determined by ATSM method D2068. In an embodiment, the treated biodiesel may pass a modified ASTM D6217 method.
In another embodiment, biodiesel incubated or stored at temperatures below ambient temperature, has a reduced Filter Blocking Tendency, as determined by ASTM method D2068.
In another embodiment, processes for removing mon.oacylglycerols from biodiesel or oils are disclosed. The monoacylgiycerols are removed by placing the biodiesel or oil in contact with a compound capable of removing the monoacylglycerols from the biodiesel or oil. By removing the monoacylglycerols from the biodiesel, the biodiesel has a reduced tendency to have a retarded flow or block filters when the biodiesel or oil is used in combination with an engine.
In another embodiment, a biodiesel placed in contact with a compound capable of removing monoacyiglycerols (i.e., treated biodiesel) has a reduced amount of monoacylglycerols as compared to a biodiesel not placed in contact with a compound capable of removing monoacylglycerols (i.e., untreated biodiesel). The treated biodiesel also has a reduced filter blocking tendency as compared to the untreated biodiesel. The treated biodiesel may have a FBT value of less than 1.414 as determined by ATSM method D2068. In an embodiment, the treated biodiesel may pass a modified ASTM D6217 method.
Since conventional tests for ascertaining the consequences of cooling biodiesel, such as pour point or cold filter plugging point, are not useful in detecting the presence of steryl glycosides, it was surprisingly found that IP387 and the ATSM method (D2068, Standard Test Method for Filter Blocking Tendency of Distillate Fuel Oils") provide measurements of filter blocking capabilities in biodiesel that has not been cooled.
The tests for measuring filter blocking capabilities herein described are carried out with a Normalab Analis (Lintot, France) NBF240 instrument. A sample (that is substantially free of undissolved water) is passed through a specified glass-fiber filter medium at 20 ml/minute. The pressure difference across the filter is monitored, and the volume of fuel passing through the filter medium within a prescribed pressure drop is measured. According to the test, the filter blocking tendency is defined on a linear scale through a discontinuity point of 105 kPa/300ml. This provides a dimensionless unit which is independent of the point of test cessation. The test ceases when the pressure difference across a specified filter reaches 105 kPa or when 300 mi of biodiesel passes through the filter, whichever is reached first. The results are reported as a volume or pressure at the point of cessation. A sampie passes the test if a 300 mi volume can pass through a filter having a 1.6 micron part icle retention and 13 mm diameter (such as Millipore Cat. No. XX30 012 00 from Millipore Corp. or Grade GF/A (FBT) from Whatman (Cat. No. 1820 8013)) without developing a pressure equal to or greater than 105 kPa. A sample fails the test if the pressure reaches 105 kPa before 300 ml of biodiesel is passes through the filter.
In this embodiment, filter blocking tendency (FBT) can be described in one of the following ways: the pressure drop across a 1.6 pm pore size glass fiber filter when 300 mL of fuel is passed at a rate of 20 mL/min, or the volume of fuel passed when a pressure of 105 kPa (15 psi) is reached. The latter method is used when less than 300 mL passes at a rate of 20 mUmin before the pressure exceeds 105 kPa. A sample of the fuel to be tested is passed at a constant rate of flow (20 mlJmin) through a glass fiber filter medium. The pressure drop across the filter is monitored during the passage of a fixed volume of test fuel. If a prescribed maximum pressure drop is reached before the total volume of fuel is filtered, the actual volume of fuel filtered at the time of maximum pressure drop is recorded.
Before the test, the temperature of biodiesel being sampled is adjusted to about 15 to 25 C. The biodiesel is shaken vigorously for about 120 seconds (plus or minus 5 seconds), and allowed to stand on a vibration-free surface for about 300 seconds. A sample of about 320 mL, plus or minus 5 mL, is placed into the fuel reservoir beaker of the Normalab Analis NBF240 instrument and the temperature is checked to ensure that it is within the range of about 15 to 25 C (the actual temperature is recorded). The pump suction pipe of the instrument is placed into the fuel reservoir beaker. The pump is run until biodiesel flows from the fitting to which the filter unit is attached into the collection beaker. The pump is stopped, and any fuel from the collection container is poured back into the fuel reservoir beaker. The filter unit is assembled with a fresh filter, and the assembled filter unit is attached to the instrument through a Luer fitting. The pump and stopwatch are started, and after about 20 seconds, the pressure gauge reading is recorded. If the pressure gauge reading falls in the range of about 7 to 21 kPa, pumping is continued at 20 mi/minute and the pressure gauge is monitored continuously. If the pressure rises to 105 kPa, the pump is stopped immediately and the volume of liquid that passed through the filter at that point is reported as v. If the pressure does not rise to 105 kPa after 300 mL has passed through the filter, the highest pressure reached in the test is reported as P.
.Filter blocking tendency (FBT) is calculated using one of the following equations, depending on whether a value was obtained for v or P.

FBT = 4 1+ (P/105)2 = (Square root of (1+ (P/105)2), or (1+ (P/105)2)'i' FBT 1+ (300_)2 = (Square root of (1+ (300/v)2), or (1 + (300/v)2)'' P is the maximum pressure reading obtained for 300 mL of biodiesel to pass through the filter, in kilopascals; and V is the volume of fuel passed at a pressure reading of 105 kPa, in milliliters.
FBT is expressed as a dimensionless number to the nearest 0.01. A FBT value close to 1 indicates good flow characteristics, and an FBT
value of 1.414 or greater indicates poor flow and indicates that the fuel failed the FBT test. As the minimum test volume is 20 mi, liquids which exceed 105 kPa pressure in 20 ml or less are assigned the greatest FBT value that can be determined (i.e., 15.03).
An alternative method of testing biodiesel is a modified ASTM6217 test. The modified ASTM6217 test is carried out as follows:
biodiesel (300 ml) is filtered through a 1.6 um GF/A filter having 47 mm diameter under a 21-25-inch Hg vacuum. The entire volume of 300 ml of the biodiesel must pass through the filter in an predetermined amount of time, such as 30 minutes, 15 minutes, 12 minutes, 10 minutes, 9 minutes, 8 minutes, 7 minutes, 6 minutes, 5, minutes, 4 minutes, 3 minutes, 2 minutes, 1 minute, or fractions thereof.
In order to produce biodiesel having an acceptable FBT value or pass a modified ASTM6217 test, the biodiesel may be treated to obtain an acceptable FBT value or pass a modified ASTM6217 test using methods of the present invention. Some conventional treatments to the biodiesel do not produce an acceptable FBT value or biodiesel that passes a modified ASTM6217 test. For instance, biodiesel that is water washed to remove water-soluble impurities does not remove the steryl glycosides since the steryl glycosides are poorly soluble or insoluble in water. Thus, biodiesel treated by water washing contained 34 ppm steryl glycosides and failed the FBT test by exceeding 105 kPa pressure in less than 20 mL of the biodiesel.
Another conventional treatment of biodiesel is distillation.
Although the distillation of the biodiesel may produce a biodiesel having an acceptable FBT value or that may pass a modified ASTM6217 test, the distillation procedure is not economically acceptable. Thus, even though a commercial sample of biodiesel subjected to a distillation procedure contained no detectable steryl glycosides and had an FBT value of 1.01, the distillation procedure is costly. For instance, purification by distillation is expensive and inefficient. Further, the entire finished biodiesel product must be distilled by conventional means such as over a column or on a wiped film evaporator, necessitating costly inputs of energy to heat and cool the biodiesel. In addition, as biodiesel contains large amounts of heat-sensitive compounds, such as esters of olefinic fatty acids, the elevated temperatures required for distillation will accelerate the breakdown of the biodiesel, such as by lipid oxidation, leading to reduced storage stability of the distilled biodiesel.
Alternatively, costly measures to store the biodiesel, such as the addition of antioxidants or blanketing with an inert gas, may be required.
In various embodiments described herein, an improved biodiesel having a reduced filter blocking tendency, as defined by test IP387 (and ASTM
Method D2068, "Standard Test Method for Filter Blocking Tendency of Distillate Fuel Oils") is prepared using the processes herein. By treating biodiesel with solid compounds, a treated biodiesel having a reduced filter blocking tendency than the starting biodiesel is produced. The improved biodiesel has a decreased amount of steryl glycosides. In some embodiments, the improved biodiesel has a decreased amount of monoacylglycerols. Further, it is desired that the improved biodiesel is able to flow at temperatures of 0 C and below.
Suitable solid compounds that may be used include, but are not limited to, adsorbents, filter aids, water-soluble solids, water-soluble bed materials, and any combinations thereof.
In one embodiment, a bed of solid bed material is associated with a filter and used to treat biodiesel by passing the biodiesel through the bed, thus, removing steryl glycosides from the biodiesel.
In an embodiment, a bed of solid bed material is associated with a filter and used to treat biodiesel by passing the biodiesel through the bed, thus, removing monoacylglycerols. In an embodiment, the compound can be applied to a filter as a precoat, wherein a layer of the compound is deposited on a filter and biodiesei is fiftered by passing through the fiiter and the layer of the precoat_ To apply a precoat, the desired quantity of compound is slurried in a small amount of biodiesel and the slurry is passed over or through the filter, such as a filter screen. The biodiesel passes thought the filter, leaving a thin layer of the compound on the screen for subsequent use in filtering biodiesel.
In an embodiment, the compound can be applied to biodiesel as a body feed, wherein the compound is mixed with biodiesel and the mixture of the compound and the biodiesel is passed through a filter. In another embodiment, the compound mixed with biodiesel as a body feed may be passed through a filter and a layer of precoat.
In another embodiment, solid compounds may be added to biodiesel and slurried before removal of the solid compounds by passing the biodiesel/solid compound slurry through a filter. Solid bed materials that may be used include, but are not limited to, water-soluble solid bed materials. When water-soluble solid bed materials are used to treat the biodiesel, the solid bed material can be washed with solvent to remove any residual biodiesel. The water soluble solid bed material may also be dissolved in water to obtain a material enriched in steryl glycosides. Thus, in another embodiment, a process for purifying or obtaining steryl glycosides is disclosed.
In an additional embodiment, indicia are associated with biodiesel treated by the methods or processes of the present disclosure to inform the purchaser, distributor, blender or consumer of treated biodiesel that the treated biodiesel passes a filter blocking test or a modified ASTM6217 test.
In another embodiment, the indicia may disclose the results of a filter blocking tendency test result or a modified ASTM6217 test. In another embodiment, the indicia may inform the purchaser, blender, distributor or consumer that the biodiese( has been treated to reduce the content of steryl glycosides and/or monoacylglycerols in the biodiesel. In yet another embodiment, indicia are associated with the treated biodiesel to provide or disclose the content of steryl glycosides.
In an embodiment, a period of incubation of biodiesel prior to filtration may be employed. In an embodiment, the temperature of incubation or storage may be below the manufacturing temperature. The duration of incubation prior to filtration may be 15 minutes, 30 minutes, 1 hour, 2 hours, hours, 6 hours, 8 hours, 10 hours, 12 hours, 18 hours, 24 hours, 2 days, 3, days, 4 days, 5 days, 6 days, 1 week, 2 weeks, 3 weeks, 4 weeks, I month, 2 months, 3 months, 4 months, 5 months, 6 months, or fractions of any thereof.
In an embodiment, the temperature may be zero degrees Fahrenheit (-18 C), 10 degrees Fahrenheit (-12 C), 20 degrees Fahrenheit (-7 C), 30 degrees Fahrenheit (-1 C), 40 degrees Fahrenheit (4 C), 50 degrees Fahrenheit (10 C), 60 degrees Fahrenheit (16 C), 70 degrees Fahrenheit (21 C), 80 degrees Fahrenheit (27 C), 90 degrees Fahrenheit (32 C), 100 degrees Fahrenheit (38 C), 110 degrees Fahrenheit (43 C), 120 degrees Fahrenheit (49 C), or fractions of any thereof. Following the incubation, the biodiesel may be filtered such as through a polishing filter, a bag filter, a sock filter, a dewaxing filter or any combination thereof. In an embodiment, filtration may employ the use of a compound in the form of a body feed, a precoat, or combinations thereof. In another embodiment, biodiesel my be incubated or stored for a second period prior to being subjected to a test to determine filterability, such as ASTM
Method D2068 or a modified ASTM D6217 test.
The invention is further explained by use of the following illustrative examples.
In one embodiment, biodiesel was tested to see if the biodiesel has an acceptable FBT value. Commercially manufactured rapeseed biodiesel that was subjected to a final polishing filtration step through a final sock filter having 1 micron pore size at 14,250 kg/hour was obtained. Filter blocking tests were performed on the rapeseed biodiesel using a Normalab Analis (Lintot, France) NBF240 instrument according to IP387 (and ASTM Method D2068, Standard Test Method for Filter Blocking Tendency of Distillate Fuel Oils, ASTM
International. The ASTM standards may be obtained from the ASTM website at www.astm.org). The biodiesel flow through the polishing sock filters was unimpeded and the FBT value of the finished biodiesel was 1.02 (maximum pressure reached in filtration of 300 mi biodiesel was 21 kPa).
In another embodiment, fatty acids recovered from a glycerol-rich heavy phase of biodiesel manufactured by the process of US Patent No.
5,354,878 (which is hereby incorporated in its entirety by reference) were used as feedstock to synthesize biodiesel using hydrochloric acid as a catalyst.
These fatty acids are referred to as "acid oil". The following amounts of reactants were used to synthesize the biodiesel: 100 parts fatty acid, 100 parts methanol, 3 parts hydrochloric -acid, and 180 minutes of incubation with heat and stirring in a 1000 liter vessel. The resulting biodiesel (780 kg) was blended into the 14,250 kg/hour flow of rapeseed biodiesel going to the filters over the course of 2 hours (390 kg/hour). The FBT of the blended biodiesel increased steadily until it reached a peak of 1.69 and failed the FBT test by reaching kPa pressure after filtering only 220 ml. Solid material on the final bag filter having 1 micron pore size was tested by thin-layer chromatography and a spot having a retention factor equal to a steryl glycoside reference was observed.
Both Nuclear Magnetic Resonance and gas chromatography with mass spectroscopy determined that the solid material on the final bag filter having micron pore size contained sterol and sugar structures.
Commercially manufactured soy biodiesel which had not been subjected to simple final filtration through a polishing filter was obtained.
This unfiltered soy biodiesel was subjected to filtration treatments through compounds, wherein the biodiesel was placed in contact with a compound for removing steryl glycosides from the biodiesel. The compounds in this example included granular glucose, granular sugar, diatomaceous earth, and granular clay. A Buchner funnel was fitted with #1 filter paper (3.8 cm diameter, 11.3 cm2 filter area, >11 micron particle retention) and beds of the various solid bed materials (i.e., compounds for removing the steryl glycosides) were prepared.
The amount of time required to pass 50, 100, 150 and 200 ml of room temperature biodiesel through the filter was determined (Table 1). Studies were carried out in dupiicate_ Table 1. Filtration volumes and times for biodiesel passed through compounds. Diatomaceous earth (DE) was FW20 from Eagle Picher, Phoenix, AZ. Granular clay was Agsorb 30/60 LVM-GA from OilDri, Chicago, IL.

Filtration Time (sec) Filter Cake Filter Volume 50 100 150 200 thickness mt (mm) Control #1 a er 12 67 181 250 --Granular 15 67 130 220 15 Glucose 15 Granular Sugar 4 15 28 42 12 Granular Clay 42 110 192 295 14 (1Q g) The content of steryl glycosides in the unfiltered biodiesel was estimated to be 70-90 ppm obtained by ascertaining the increase in weight that occurred with the granular sugar used as a solid bed material. The filter paper with no additional solid bed material was blinded or coated quickly with a gummy deposit, resulting in slow filtration (long filtration time). After filtering biodiesel through filter paper with no additional solid bed material at room temperature, the steryl glycosides content of the filtered (i.e., treated) biodiesel was 50ppm. Granular glucose, granular sugar and diatomaceous earth (DE) provided shorter filtration times. The filtration time obtained with granular clay was longer than the other solid bed materials. The shortest filtration time, and thus the fastest flow, was obtained with granulated sugar, while a constant filtration rate was obtained with diatomaceous earth DE.

Magnesium silicate (Magnesol R30, Dallas Group, Whitehouse, New Jersey) was tested as a "body feed" for treating biodiesel having a steryl glycoside content of 174 ppm and visible haze. Unfiltered biodiesel (180 g) was slurried at room temperature or at 60 C with Magnesol R30 (added as "body feed" to the biodiesel) for 10 minutes. The slurry was filtered through Whatman #1 filter paper at room temperature. The steryl glycoside content in biodiesel before and after Magnesol treatment and filtration was measured. The filtered biodiesel was also subjected to a Cold test (AOCS Official Method Cc11-53) to evaluate the reduction of haziness. A procedure of the cold test is found in "Official Methods, and Recommended Practices of the AOCS", Fifth Edition, Second Printing (2004) American Oil Chemists' Society, Champaigri, IL, which is incorporated herein in its entirety by this reference. For the cold test, 4-oz.
clear sample botties were filled with biodiesel before immersion in an ice water bath maintained at 0 C. The sample bottles were removed from the ice water bath every hour to examine the appearance of the biodiesel for haziness. To pass the test, the biodiesel samples should be completely clear and brilliant.
Table 2. Filtration of biodiesel with Magnesol R30 at room temperature (RT).

R30, % R301 g Filter time, Appearance SG content Cold test sec. at RT (ppm) @ 4 hours 0.2 0.36 84 clear 34 fail 1.2 2.16 202 clear 35 Pass Table 3. Filtration of biodiesel with Magnesol R30 at 60 C.

30, % 30, g Filter Appearance SG content Cold test '?a 6 time, sec. at RT (PPM) hours .2 .36 33 clear 74 borderline .2 .16 108 clear 41 pass All levels of Magnesol R30 treatment were effective at reducing the appearance of haze at room temperature and 60 C. The appearance of haze or lack of appearance of haze at room temperature in biodiesel treated at room temperature and treated at 60 C was used as a qualitative assessment of possible steryl glycoside content. Room-temperature magnesium silicate treatment was more effective at reducing the quantity of steryl glycosides in biodiesel than treatment at 60 C, and also produced a biodieset which passed a cold test at 4 hours (Tables 2 and 3). However, the ability of the biodiesel to pass the cold test after filtration at room temperature was unrelated to the steryl glycosides content of the biodiesel, indicating that the cold test was not actually measuring steryl glycoside content, but rather measuring some other component (i.e., possibly the crystals rich in saturated fatty acid ester which develop under cold conditions).
Samples of biodiesel filtered with 1.2% Magnesol at room temperature and 60 C were analyzed to determine the effectiveness of Magnesol treatment at reducing the content of monoacylglycerols and the results are presented in Table 4.
Table 4. Monoacylglycerol reduction by treatment with Magnesol R30.

Monoacylglycerols (%) No Magnesol (control) 0.72 L1.2% Magnesol at room temperature 0.61 1.2% Magnesol at 60 C 0.59 Cooling the biodiesel was not required to reduce the content of monoacylglycerols. A reduction of 15% was effected at room temperature and a reduction of 17% was effected at 60 C.

Water-soluble compounds (i.e., sugar, sodium chloride, and citric acid) were compared with DE for their ability to remove steryl glycoside from biodiesel and produce improved biodiesel. Commercial biodiesel (600 g) having a steryl glycoside content of 174 ppm was filtered through the water-soluble solid bed materiais (14 grams of granular sugar, sodium chloride (NaCI) or citric acid) or diatomaceous earth (DE, 5 grams) on a Whatman #1 filter paper (3.4 cm diameter) under vacuum. Residual biodiesel was removed from the sugar, sodium chloride, and citric acid filter cakes by washing with -100 mi hexane and hot water (-70 C, 200 ml), which was used to dissolve the solid bed materials and recover the steryl glycosides. The recovered steryl glycosides remaining on the filter paper were dried in a 70 C oven overnight.
Table 5. Steryl glycoside content and filter blocking tendencies of biodiesel treated with solid bed materials.

Solid bed FBT value SG (ppm) 1[- SG reduction (%) material None (control) 15.03 174 --Granular sugar 1.14 22 87.3 NaCI 1.05 22 87.3 Citric acid 1.05 22 87.3 DE 1.01 39 77.6 Excellent Filter Blocking Tendency (FBT) values and reduction of steryl glycosides of from 77.6% to 87.3% were obtained with the solid bed materials tested (Table 5).

EXAMPLE'5 A sample of unfiltered commercial soy biodiesel having 117 ppm steryl glycosides and filtered commercial soy biodiesel (having 68 ppm steryl glycosides) produced at the same facility were subjected to the Filter Blocking Test. The unfiltered and the filtered soybean biodiesel failed the FBT test by exceeding 105 kPa pressure after 20 miJ to yield FBT values of 15.03. The filtered soy biodiesel (1000 g) was passed through a bed of 5 grams of diatomaceous earth at room temperature to yield a treated biodiesel having a steryl glycoside content of 20 ppm which passed the FBT test with an FBT value of 1.01.

The commercial unfiltered soy biodiesel from Example 5 (1000 g) was filtered through a 5 gram bed of diatomaceous earth (DE) at room temperature and at 60 C using the procedure of Example 4. The biodiesel filtered through the diatomaceous earth at room temperature had an FBT value of 1.01 and contained 34 ppm steryl glycosides. The biodiesel filtered through diatomaceous earth at 60 C had an FBT value of 1.20 and contained 39 ppm steryl glycosides.

Diatomaceous earth was tested as a "body feed" for treating biodiesel. Commercial soy biodiesel (555 g) was treated by slurrying the soy biodiesel with 5 g DE (Altofina Clarcel DIT/2R SA 25K, AltoFina, King of Prussia, PA), stirring the slurry for 10 minutes at 500 rpm, and filtering the slurry through a 0.95 cm deep bed of DE on a 4 cm diameter Schleicher & Schuell "White Ribbon Filter" filter paper (Grade 598/2: 4-12 micron retention, ashless standard filter paper for medium fine precipitates (class 2b according to DIN

135, from VWR/Sargent Welch Scientific Co., Buffalo Grove, IL). The filtration was carried out at room temperature and the filtrate was. cooled to 1 C. After cooling, the filtrate was analyzed to measure the FBT and contents of glycerol esters in the untreated and treated biodiesels. The results are shown in Table 6.
Table 6.

Temperature FBT Monoacylglycerols Diacylglycerols Triacylglycerols Untreated 15.03 0.639 % 0.159 % 0.0174 %
RT (--'25 C) 1.03 0.624% 0.160% 0.0169%
1 C 1.03 0.616% 0.158% 0.0171 %
Although the content of glycerol esters was virtually unchanged by the filtration treatment at both temperatures, the FBT values were greatly affected. The unfiltered biodiesel failed the FBT test after only 20 ml had passed through the FBT filter, but the treated biodiesel showed excellent FBT
values, showing that improvement of FBT by filtering through DE under these conditions was not dependent on removal of the glycerol esters that can cause filter blockage.
A purified steryl glycoside composition was prepared by filtration through granulated sugar. After treating 1000 mL of soy biodiesel with a bed of granular sugar (15 g, 1.2 cm deep) as described in Example 4, the bed of granular sugar was washed with hexane to remove the biodiesel from the bed of granular sugar. The composition of soy biodiesel is given in Table 7. Warm wash water was applied to the carbohydrate solid bed material (granular sugar).
The solid bed material that dissolved in the wash step left behind a steryl glycoside composition comprising 92% steryl glycoside.
The entire lot of treated biodiesel was refrigerated for 3 days at 2.2 C (36 F). A visible cloud formed. The treated, refrigerated biodiesel was filtered through a second bed of granular sugar (approximately 2 cm in depth).
The filter bed was washed with cold (-6 C) hexane. Water was applied to the second bed of granular sugar to dissolve the sugar, and material remaining on the filter was recovered. This material was washed with water and dried at 70 C. The material partially melted and formed a waxy solid when cooled. The waxy solid was predominantly monoacylglycerols (>90%, Table 7) and contained 0.67 % steryl glycosides.

Table 7. Composition of biodiesel and waxy solid.
Sampte Id Commercial Waxy solid biod'iesel -7 Fatty acid methyl esters 97.89 4.81 Monoacylglycerols 0.74 94.01 Diacylglycerols (DAG) 0.27 1.03 Triacylglycerols (TAG) <0.01 <0.01 Free fatty acids 0.12 0.06 Free glycerol <0.01 0.10 The monoacyiglycerol-rich waxy solid was enriched in (greater than 92%) of saturated monoacylglycerols (Palmitic C16:0 and Stearic C18:0, Table 8).

Table 8. Fatty acid composition of waxy solid.

I Sample [_Commercial biodiesel Waxy solid Paimitic C16:0 10.24 53.15 Stearic C18:0 4.40 32.73 Oleic C18:1 n9 cis 21.87 2.05 Linoleic C18:2n6 cis 50.48 3.31 Linolenic C18:3n3cis 7.70 0.58 Total Saturated FAs 15.81 92.59 E?CAMPLE 9 Biodiesel containing 22 ppm steryl glycosides was obtained by combining the biodiesel filtered through sodium chloride (22 ppm steryl glycosides) obtained in Example 4 with the biodiesel filtered through citric acid (22 ppm steryl glycosides) obtained in Example 4. Purified steryl glycosides obtained using the treatment of Example 8 were added at known levels (10, 30, and 50 ppm) to the biodiesel to produce biodiesel of various steryl glycosides contents, which were subjected to the Filter Blocking Tendency test (Table 9).
Table 9. FBT values of biodiesel with added steryl glycosides.
Steryl glycoside content FBT value 22 ppm (control) 1.05 32 ppm 1.47 52 ppm 2.90 72 ppm 15.03 All of the biodiesel samples containing additional steryl glycosides failed the FBT (FBT values greater than 1.414). EXAMPLE 10 Soy biodiesel (400 g) having an FBT value of 15.03 was blended with 12 grams of deoiled soy lecithin and subjected to a degumming procedure.
The mixture was heated and mixed vigorously to disperse the lecithin in the biodiesel. Deionized water (12 grams) was added to the mixture and the mixture was agitated gently for about 20 minutes. The mixture was subjected to centrifugation, cooled to 40 F (4 C) and held at that temperature for 16 hours.
The mixture was allowed to warm to room temperature and subjected to the filter blocking tendency test. The FBT value of biodiesel treated in this manner was 1.02 (passed). The heavy phase is expected to be enriched in steryl glycosides.

Commercial unfiltered biodiesel (1000 g, labeled "Feed BD") at room temperature, i.e., -72 F (-22 C), was divided into two lots, and each lot was passed through a separate bed of diatomaceous earth (DE) (5 g). The DE
filter cake was labeled "DE fiiter cake" and the biodiesel that had passed through the filter was labeled "DE filtered BD". Each filter cake was washed with 200 mi room temperature hexane. One lot of filtrate (DE filtered BD) was evaluated by the Filter Blocking Test and an FBT value of 1.01 was obtained.
The other lot of filtrate (DE filtered BD) was cooled for 72 hours in a cold bath at 37 F (3 C) and divided into two sublots of 250 g.
Each sublot of DE filtered BD was filtered through separate beds of 15 g granular sugar and the filtrates were combined, labeled "37 F (3 C) DE
filtered, cooled BD final" and analyzed. The sugar filter beds were washed with 200 mi cold (-5 C) hexane and the hexane wash filtrates were combined, evaporated to remove hexane, labeled "37 F (3 C) DE filtered, hexane filtrate,"
and analyzed. The combined sugar filter beds (DE filtered, hexane residue) were washed with 200 mi room temperature water to remove sugar. The filter paper from the sugar beds was dried at room temperature and the solid residue on the filter paper was labeled "37 F (3 C) twice filtered solid bed" and analyzed. The results of the analysis are shown in Table 11.
Table 11.

37 F (3 C) 37 F (3 C) 37 F
(3 C) DE filter DE bE DE twice-cake BD filtered filtered, filtered, cake BD cooled tiexane filtered BD final filtrate solid bed MAG 0.71 0.72 0.72 0.72 0.71 95.24 %
DAG 0.15 0.2 0.2 0.18 0.15 0.02 %
TAG 0.12 0.0 0.0 0.0 0.02 0 %

(ppm) FBT 15.03 --* 1.01 1.01 --* - *
* not measurable When biodiesel having a MAG content of 0.71% was filtered through DE, cooled and filtered through sugar, the biodiesel passed easily and quickly through the bed of sugar, and the content of monoacylglycerol (MAG) was virtually unchanged. The small amount of "37 F (3 C) twice filtered solid bed" (0_2907 g) obtained by treating biodiesel with DE at room temperature, cooling the biodiesel, filtering through sugar, washing the sugar filter bed (filter cake) with cold hexane, and washing the sugar filter bed with room temperature water was almost exclusively monoacylglycerols (greater than 95%) and was enriched in steryl glycosides (SG, 654 ppm).

Commercial unfiltered biodiesel used in Example 1_1 (500 g, labeled "Feed BD") was cooled for 72 hours in a cold bath at 37 F (3 C) and divided into two sublots of 250 g. Each sublot was filtered through separate beds of 15 g granular sugar and the filtrates were combined, labeled "Filtered BD final," and analyzed. The sugar filter beds were washed with 200 ml cold (-5 C) hexane and the washed filter beds were combined, labeled "All cooled hexane residue," and analyzed. The sugar filter bed was washed with 200 mi room temperature water. The filter paper was dried at room temperature and the solid residue on the filter was labeled "All cooled solid residue" and analyzed. The results of the analysis are shown in Table 12.
Table 12.

Filtered All cooled All cooled Feed BD BD final hexane residue solid residue MAG ( lo) 0.71 0.65 0.78 63.97 DAG (%) 0.15 0.2 0.15 0.13 TAG ( 1a) 0.12 0.03 0.01 0.08 SG (ppm) 65 27 27 155699 FBT 15.03 1.01 -*
* not measurable on this material The flow of cooled biodiesel through sugar beds was not rapid as it was in Example 11. This filter treatment reduced the content of MAG in biodiesel, the content of SG decreased from 65 to 27, and the resulting biodiesel had excellent properties in the Filter Blocking Test.

Commercial soy methyl esters containing 56 ppm steryl glycoside failed the filter blocking test (FBT) with a filter plugging tendency value of 30Ø Two solvents were tested as co-solvents for the methyl esters;
dimethyl acetamide (DMA, boiling point 164 C) and methyl-s-pyrrolidinone (methyl pyrrolidone, boiling point 202 C). Solvents (33 ml, 10 v/v%) were mixed with 297 ml commercial soy methyl esters and stirred with a magnetic stirrer overnight at room temperature, and filter plugging tendencies were measured by FBT. The filter plugging tendencies were improved as shown in table 13. In another test, the methyl esters/solvents mixtures were stirred with a magnetic stirrer for 6 days at room temperature, then FBT were measured. The FBT
passed the test (Table 13).

Table 13. FBT of biodiesel with added solvents Filter plugging tendency -3 Overnight treatment 6-day treatment With 10% DMA 1.44 (fail) 1.06 (pass) With 10% pyrrolidone 1.80 (fai!) 1.05 (pass) Semisolid material (final filter cake) retained in a production scale sock filter in a final polishing filtration step of biodiesel manufacture (30 g) was mixed with 1000 ml diethyl ether on a magnetic stirrer for 10 min. After rriixing, the mixture was centrifuged at 3000 rpm for 30 sec, and the solvent phase was decanted. Hexane (1000 mi) was mixed with the pellet for 30 minutes, and the mixture was centrifuged and decanted the same way for a total of three hexane washes. The pellet was recovered and filtered through #1 filter paper to provide a residue cake. The residue cake was oven dried at 70 C
overnight. About 3.4 g of material was recovered and analyzed. The material was steryl glycoside of 99.8% purity.

Steryl glycosides were measured in biodiesei made from once-refined (OR) soybean oil (ADM, Decatur, IL) and refined, bleached (RB) soybean oil (ADM Quincy IL). OR Soybean oil contained 189 ppm steryl glycosides, and RB soy contained 224 ppm stery! glycosides. Samples of each oil were subjected to biodiesel synthesis. About 500 ml oil was taken up in a round bottom flask and heated to 90 C under house vacuum for 15 minutes to remove traces of water. Dried oil (436 grams) was mixed with anhydrous methanol (90.0 g) to provide a molar ratio of triacylglycerols/methanol of 1/6 in a one-liter Erlenmeyer flask. A magnetic stir bar was placed in the flask and , stirring was started. To the oil/methanol mixture was added 30% sodium methoxide catalyst solution (7.6 ml; 0.5 wt% sodium methoxide based on oil weight). This mixture was refluxed for 30 minutes, when the vessel was removed from heat and cooled under reflux until boiling ceased. The reaction mixture was transferred to a one-liter separatory funnel and held for 10 minutes to separate. A phase separation took place, and the lower phase (glycerol phase) was drained from the separatory funnel. The reaction mixture (biodiesel) was transferred to a one-liter round bottom flask and washed by mixing with 44 ml warm (-70 C) water with agitation. After ten minutes, the bottom phase was removed with a pipette and the wash procedure was repeated twice for a total of three washes. The washed biodiesel was transferred to a separatory funnel, remaining visible wash water was removed, and the biodiesel was dried by heating to 90 C under house vacuum and holding for 20 minutes. The.wash waters were combined and concentrated by evaporation on a rotary evaporator.
After biodiesel synthesis, steryl glycosides were concentrated in the wash water (Table 14).

Table 14. Steryl glycoside content (ppm) in biodiesel process streams made from once-refined (OR) and refined, bleached (RB) soybean oil.
SG in biodiesel SG in biodiesel from OR oil (ppm) from RB oil (ppm) Feed oil 189 224 Transesterification reaction 78 64 mixture Glycerol phase ND ND
Ester phase after water wash 59 ND
Wash water concentrate 1054 2294 ND: not detected Commercial soy biodiesel (B.100, comprising 100% soy biodiesel) containing 58 ppm steryl glycosides was mixed with petroleum diesel fuel obtained from a local filling station to obtain blends (Table 15) which were S subjected to the Filter Blocking Test. The petroleum diesel fuel had a cloud point of -19.6 C, which is in the range of Number 2 diesel fuel. B100 and B10 failed the filter blocking test, but blends incorporating 2% and 5% biodiesel in conventional diesel (B2 and B5, respectively) passed the filter blocking test (Table 15).
Table 15. Blends of commercial biodiesel and conventional petroleum diesel fuel.

Biodiesel content (%T7- Designation FBT Value Pass/Fail 2% B2 1.01 Pass 5% B5 1.07 Pass 10% B10 1.74 Fail 100% B100 Fail Commercial soy biodiesel (B100, comprising 100% soy biodiesel) containing 58 ppm steryl glycosides was subjected to filtration through diatomaceous earth substantially as described in Example 5 to produce a B100 with reduced content of steryl glycosides (37 ppm). The B100 with a reduced content of steryl glycosides and blends with petroleum diesel (B10 and B20) passed the filter blocking test (Table 16).
Table 16. Blends of filtered commercial biodiesei and conventional petroleum diesel fuel.

Biodiesel content (%) Designation FBT value {_Pass/Fall 10% B10 1.01 Pass 20% B20 1.03 Pass 100% B 100 1.01 Pass Commercial soy biodiesel having a steryl glycoside content of 69 ppm failed when subjected to the filter blocking test. The effects of incubation of biodiesel at certain temperatures before and after filtration through diatomaceous earth on steryl glycoside content and FBT tendency were tested.
A sample of biodiesel (1 liter) was held overnight at 70 C and incubated in a water bath at a first temperature of 70 F (21 C) (Table 17A), 50 F (10 C) (Table 17B), or 40 F (4 C) (Table 17C) for a first incubation time. The incubated biodiesel (500 mi) was filtered through a 5-gram precoat of diatomaceous earth, incubated at a second temperature for a second period as indicated in Table 17A, 17B, and 17C, and subjected to the filter blocking test, and the content of SG was determined.
Table 17A. First incubation at room temperature (70 F (21 C)).
First Second Second Pressure, Steryl Test Incubation Incubation Incubation Filter Glyco-Time Temperature Time Blocking sides Test (kPa) (ppm) Control 16 hours none none 6.08 ND*
17-1 6 hours 40 F (4 C) 16 hours 1.01 38 17-2 6 hours RT 3 days 1.01 32 17-3 1 day RT 3 days 1.01 19 17-4 2 days RT 3 days 1.02 16 17-5 3 days RT 3 days 1.01 17 *nd, not determined due to failure on FBT test Table 17B. First incubation at 50 F (10 C).

Pressure, Steryl First Second Second Filter Glyco-Test Incubation Incubation Incubation Blocking sides Time Temperature Time Test (ppm) (kPa) Control 16 hours none none 3.16 ND*
17-10 6 hours 40 F (4 C) 16 hours 1.01 38 17-11 6 hours RT 3 days 1.01 27 17-12 12 hours RT 3 days 1.01 21 17-13 1 day RT 3 days 1.01 21 *nd, not determined due to failure on FBT test Table 17C. First incubation at 40 F (4 C).

Pressure, Steryl First Second Second Filter Glycosi Test Incubation Incubation Incubation Blocking des Time Temperature Time Test (ppm) kPa Control 16 hours none none 15.03 ND*
17-6 6 hours 40 F (4 C) 16 hours 1.01 33 17-7 6 hours RT 3 days 1.01 22 17-8 12 hours RT 3 days 1.01 25 17-9 1 day RT 3 days 1.02 60 *nd, not determined due to failure on FBT test Heating biodiesel to 70 C overnight followed by incubating biodiesel at room temperature, or cooling biodiesel to 40 F (4 C), or 50 F
(10 C) for as little as six hours before filtering through a filter aid, proved to be an effective means of reducing steryl glycosides and improving filter blocking test results after a second incubation at 40 F (4 C) or room temperature (Tables 17A, 17B and 17C).

Commercial soy biodiesel having a steryl glycoside content of 69 ppm failed when subjected to the filter blocking test. The effects of treatment of biodiesel with activated carbon were tested by stirring the carbon with soy biodiesel. A sample of biodiesel (1 liter) was heated overnight at 70 C. This heated biodiesel (500 mi) was stirred with carbon (SA4 carbon, Norit Americas, Inc. Marshall, Texas) in a water bath at a first temperature of 70 C for one hour.
The incubated biodiesel (500 ml) was filtered at 70 C through filter paper to remove the carbon, incubated at a second temperature (RT) for a second period (three days), and tested to determine the filter blocking tendency and the content of SG.
Table 18A. Effect of carbon treatment with two incubation periods on FBT and steryl glycoside content.

Carbon Second Second Pressure, Steryl Test Added Incubation Incubation Filter Glyco-( 10) Temperature Time Blocking sides Test (kPa) (ppm) 18-1 0.25 RT 3 days 1.02 37 18-2 0.5 RT 3 days 1.02 35 1118-3 1.0 RT 3 days 1.02 28 Carbon treatment was effective in reducing the FBT and steryl glycoside content of biodiesel (Table 18A).
Commercial soy biodiesel having a steryl glycoside content of 69 ppm failed when subjected to the filter blocking test. The effects of treatment of biodiesel with SA4 carbon or PWA carbon (Calgon Carbon Corp, Pittsburgh, Pennsylvania) were tested by stirring with soy biodiesel. A sample of biodiesel (1 liter) was heated overnight at 70 C. This heated biodiesel (500 ml) was stirred with carbon in a water bath at a first temperature of 70 C for one hour.
The incubated biodiesel (500 ml) was filtered at 70 C through a precoat of diatomaceous earth, incubated at a second temperature for a second period, and tested to determine the filter blocking tendency and the content of SG.
Table 18B. Carbon treatment and DE filtration.

Carbon Filter Second Second Pressure, Steryl Test Added, DE Incubation lncubation Filter Glyco-amount Temper- Blocking sides ( ~0) ature Time Test (kPa) ( pm) 18-4 SA4,0.5% 1 g DE 40 F (4 C) 20 hours 1.16 39 18-5 SA4,0.5% Ig DE RT 7 days 1.39 39 18-6 PWA,1.2% 5g DE RT 3 days 1.01 26 Carbon treatment and incubation was effective in reducing the FBT and steryl glycoside content of biodiesel (Table 18B).
Commercial soy biodiesel having a steryl glycoside content of 69 ppm failed when subjected to the filter blocking test. A sample of biodiesel (1 liter) was heated overnight at 70 C. The effects of treatment of biodiesel with CPG LF granular activated carbon (Calgon Carbon Corp. Pittsburgh, Pennsylvania) were tested by passing this heated soy biodiesel (500 ml) at 0.72 grams/minute through a bed of CPG LF granular activated carbon (11.5 grams) in a jacketed column (12 mm x 40 mm) held at 70 C. The carbon-treated biodiesel was filtered at 70 C through filter paper, incubated at a second temperature (room temperature) for three days, and tested to determine the filter blocking tendency and the content of SG. The FBT value was 1.02 and the content of steryl glycosides was 31 ppm.

Commercial soy biodiesel having a steryl glycoside content of 65 ppm and mo noacyl glycerol content of 0.71% which failed the FBT test was filtered through DE at room temperature to obtain filtered soy biodiesel having a steryl glycoside content of 33 ppm, a monoacylglycerol content of 0.72%, and an FBT value of 1.01. The filtered soy biodiesel and an unfiltered control of commercial soy biodiesel were cooled to 33 F (0.6 C) and stored at 33 F
(0.6 C). The filtered soy biodiesel remained clear for several days of incubation at 33 F (0.6 C). The unfiltered control biodiesel became visibly hazy after 1 day of incubation at 33 F (0.6 C) and this control was filtered through filter paper.
The monoacylglycerol content of the filtered control biodiesel thus obtained was reduced to 0.65% and the steryl glycoside content was reduced to 27 ppm; the solid residue (filter cake) obtained contained 63.97% monoacylglycerols. Thus, the steryl glycosides enabled removal of monoacylglycerols from the soy biodiesel by filtration, possibly by providing nucleation sites for development of haze or crystals enriched in monoacylglycerols.
Soy methyl esters containing 142 ppm steryl glycosides were washed at 150 F (66 C) by mixing with 10% of a solution containing 2% boric acid for 15 minutes. The mixture was centrifuged and the methyl ester phase dried. The resulting methyl esters contained 41 ppm steryl glycosides and passed the filter blocking test (FBT=1.04).

Soy methyl esters containing 69 ppm steryl glycosides and FBT=15.03 were treated by adding 1.2% powdered carbon (Calgon PWA) at F (-9 C) and stirring for 1 hour. The treated methyl esters plus carbon were filtered at 158 F (70 C) with 47 mm diameter #1 filter paper and 5 g of diatomaceous earth. The treated and filtered soy methyl esters contained 26 ppm steryl glycosides and passed the filter blocking test (FBT=1.01).

Soy methyl esters containing 69 ppm steryl glycosides and FBT=15.03 were treated by passing through a packed bed, of granular carbon (11.5 g Calgon CPG LF 12x40 in a 13.5 cm high x 1.5 cm diameter column) at 158 F (70 C) and a flow rate of 2 BV/hour. The FBT of the effluent methyl esters was tested (Table 19).

Table 19. FBT values of biodiesel passed through a bed of carbon.
FBT
Untreated methyl esters 15.03 Methyl esters collected 0-18 hours 1.02 Methyl esters collected 18-24 hours 1.02 Soy methyl esters containing 69 ppm steryl glycosides and FBT=15.03 were treated as described in Example 22 except that the flow rate was 4 BV/hour. The effluent methyl esters collected for 24 hours failed the filter blocking test (FBT=2.36).

E)CAMPLE 24 Soy methyl esters containing 69 ppm steryl glycosides and FBT=15.03 were treated by mixing with Norit SA4-PAH-HF carbon for 1 hour at 158 F (70 C) as a "body feed" and then filtered at 158 F (70 C) through 47 mm diameter #1 filter paper without additional filter aid precoat. The filtered methyl esters were allowed to incubate for 3 days at room temperature prior to testing for filter blocking tendency (Table 20).

Table 20. FBT values of biodiesel mixed with carbon body feed and filtered.

Carbon added (%) FBT
0.25 1.02 0.50 1.02 1.00 1.02 Soy methyl esters containing 54 ppm steryl glycosides and FBT=15.03 were incubated for 6 or 12 hours at 40 F (4 C) or 50 F (10 C) prior to filtering with 5 g diatomaceous earth and the filtered soy methyl esters were tested for filter blocking tendency (Table 21). All 4 samples passed the filter blocking test (FBT=1.01-1.02). For comparison, fresh soy methyl esters containing 69 ppm steryl glycosides and FBT=15.03 were incubated for 1, 2, and 3 days at room temperature prior to filtering with 5 g diatomaceous earth (Table 21). All 3 of these samples also passed the filter blocking test (FBT=1.01-1.02) after storage:

Table 21. Steryl glycoside content of biodiesel after incubation and filtering through diatomaceous earth.

Incubation temperature Incubation/ Steryl glycoside content storage time (ppm) 40 F (4 C) 6 hours 22 40 F (4 C) 12 hours 25 50 F (10 C) 6 hours 27 50 F (10 C) 12 hours 21 70 F (21 C) (Room temperature) 1 day 19 70 F (21 C) (Room temperature) 2 days 16, 29 (two tests) 70 F (21 C) (Room temperature) 3 days 17, 29 (two tests) Soy methyl esters containing 69 ppm steryl glycosides and FBT=15.03 were treated with 0.5% carbon (Norit SA4-PAH-HF) as a body feed by mixing for 1 hour at 158 F (70 C) and then filtered at 158 F (70 C)with 47 mm diameter #1 paper and 1 g diatomaceous earth bed. The treated and filtered methyl esters were chilled for 20 hours at 40 F (4 C) prior to testing for filter blocking tendency; the FBT of the carbon-treated, filtered, biodiesel after incubation at 40 F (4 C) was 1.16.

Cellulose (EFC 450 from J. Rettenmaier, Rosenberg, Germany) was added to unfiltered soy methyl esters (having an FBT value of 15.03, fail) at 25 kg cellulose to 12 metric tons methyl esters and stirred for 1 hour. This mixture was used to precoat an industrial dewaxing filter to a depth of 3 mm.
Soy methyl esters (180 metric tons) were chilled and incubated (stored) for one week at 52-70 F (11-21 C), and filtered at a rate of 20 metric tons/hr through the cellulose precoat. The total back-pressure remained stable at 7.25 psig during the entire filtration process. Three samples of biodiesel filtered through cellulose taken at different times during the filter process all passed the filter blocking test (FBT=1.02 to 1.04).

Three different batches of fresh commercial soy methyl esters (one each from Mainz, Leer, or Hamburg, all of Germany) were filtered as described in Example 27. Samples of the treated methyl esters were incubated in a water bath at 40 F (4 C) for 16 hours prior to running the filter blocking test.
All three samples passed the Filter Blocking Test (FBT=1.01-1.03).

Distilled soy methyl esters were spiked with a steryl glycoside solution in pyridine such that the steryl glycoside concentration in the distilled soy methyl esters would be 25 ppm after the pyridine was removed. The mixture was treated with heat and vacuum to remove the pyridine and the methyl esters containing 25 ppm steryl glycosides were then chilled for 2, 4, and 6 hours at 40 F (4 C) prior to filtering at 40 F (4 C) with through a precoat of 5 g diatomaceous earth on 47 mm diameter #1 paper. The filtered samples were stored for 16 hours at 40 F (4 C). Samples were allowed to warm to room temperature without external heat source and then tested by the filter blocking tendency test.
Table 22. FBT values for distilled methyl esters containing 25 ppm added steryl glycosides.

Incubation time Incubation time at No. at 40 F (4 C) Filter 40 F (4 C) after FBT
before filtration medium filtration (hours) (hours) 1 0 None 0 15.03 2 2 DE* 2 5.10 3 4 DE 4 2.90 4 6 DE 6 1.20 *DE: Diatomaceous Earth Samples were prepared as described in Example 29 except that steryl glycoside concentration was 100 ppm. Samples were incubated and filtered as shown below. Samples were filtered at the incubation temperature, the filter used was 47 mm diameter #1, and 5 g of diatomaceous earth was used when applicable. All filtered samples were then incubated for 16 hours at 40 F
(4 C). The samples were allowed to warm to room temperature without external heat source and then tested for filter blocking tendency.

Table 23. FBT values for distilled methyl esters containing 100 ppm added steryl glycosides.

Incubation time Incubation Filter No. before filtration temperature medium FBT
(hours) before filtration 1 6 40 F (4 C) None 15.03 2 2 40 F (4 C) DE*

3 4 40 F (4 C) DE
4 6 40 F (4 C) DE 1.01 5 6 75 F (24 C) DE

*DE: Diatomaceous Earth Fresh soy methyl esters containing 55 ppm steryl glycosides were incubated for 6 hours at 40 F (4 C) immediately after synthesis substantially as described in Example 15 and divided into four lots. Each lot was filtered at 40 F (4 C) through 5 gram precoats of one of the following filter aids on using 47 mm diameter #1 filter paper: diatomaceous earth, Filtracel 250C cellulose, J. Rettenmaier Filtracel 250C+ cellulose, and Filtracel 450 cellulose. All filtered samples were then stored at 40 F (4 C) for 16 hours, allowed to warm to room temperature, and.tested for filter blocking tendency.
Table 24. Filter blocking tendency of treated fresh soy methyl esters.

Filter aid FBT
Diatomaceous earth 1.02 Filtracel 250C 1.03 Fitracel 250C+ 1.07 Filtracel 450 1.02 Soy methyl esters, FBT=15.03, were treated with beta-glucosidase (Sigma). A solution of 0.2 g beta-glucosidase in 40 g water was added to 400 g soy methyl esters. The mixture was heated to 104 F (40 C) at ambient pressure and allowed to stir for 24 hours. The mixture was transferred to a separatory funnel and the water phase drained. The methyl ester phase was dried for 20 minutes at 194 F (90 C) under vacuum. The dried methyl esters were stored at 40 F (4 C) for 16 hours prior to testing for filter blocking tendency (FBT=3.88).
Soy methyl esters were synthesized by incubating soybean oil with methanol and catalyst substantially as outlined in Example 15. The FBT
value of freshly synthesized soy methyl esters, after water washing three times with 10 vol% water, was 10.05 (Table 23). In some embodiments, the water washing step was eliminated and fresh soy methyl esters were treated with silica hydrogel (PQ Corporation 29-4) before or after a drying step. When methyl esters were dried as indicated in Table 23, where applicable, the reaction product was dried by incubation for 20 minutes at 90 C under vacuum and allowed to cool to room temperature. Hydrogel treatment was carried out on dried or undried methyl ester by heating methyl esters to 65 C, adding Silica Hydrogel 29-4 (PQ Corporation, Valley Forge, PA) as indicated in Table 23, and stirring for 10 minutes at 65 C. Vacuum was applied and the methyl esters and hydrogel were heated to 90 C and held at 90 C for 20 minutes. The mixture was cooled to 70 C, the vacuum was released, and the mixture was filtered through #50 (medium) filter paper in a Buchner funnel. Immediately after filtering, all samples were placed in 40 F (4 C) bath for 16 hours_ The samples were allowed to warm to room temperature and tested for filter blocking tendency.
Table 25. Filter Blocking Tendency of fresh soy methyl esters RBD soy methyl Methyl esters FBT
esters treated Water wash control Undried 10.05 (fail) 3x10%
Silica hydrogel 0.25% Dried 2.69 (fail) Silica hydrogel 0.5% Undried 6.08 (fail) Silica hydrogel 0.5% Dried 1.08 (pass) Silica hydrogel 1% Undried 1.14 (pass) Silica hydrogel 1% Undried 1.60 (fail) Silica hydrogel 1.5% Undried 1.09 (pass) Silica hydrogel 2% Undried 1.22 (pass) The silica hydrogel treatment produced methyl esters which passed the filter blocking test while eliminating the water washing step.

The filter blocking tendency test (FBT, ASTM D2068) was compared to a modified ASTM D6217 test which may be used as a biodiesel specification. The FBT test was carried out as described above. The modified 6217 test was carried out as follows: biodiesel (300 ml) was filtered through a 1.6 um GF/A filter having 47 mm diameter under a 21-25 inch Hg vacuum. To pass the test, the entire sample of 300 ml must pass through the filter in 6 minutes. In every case, biodiesel that passed the FBT test also passed the modified D6217 test. Table 26 reports the time required for 300 ml.to pass through the filter for passing samples, and the volume passed through the filter in 6 minutes for failing samples.
Table 26. Comparison of ASTM D2068 and Modified ASTM
D6217 (mis = milliliters).

Methyl ester ASTM D2068 (FBT) ASTM D6217 ME
FBT Time (min) or volume Canola 1.03 pass 0:30 pass Tallow 5.10 fail 1:30 pass Soy 2.36 fail 3:45 pass Soy 15.03 fail 130 mts fail Soy 15.03 fail 180 m{s fail Canola 4.4 fail 1:04 pass Canola 10.05 fail 200 mis fail Animal 10.05 fail 2:04 pass Poultry 15.03 fail 115 mis fail Tallow 3.88 fail 0:28 pass Soy 7.57 fail 0:55 pass Soy 15.03 fail 1:47 pass Soy 1.01 pass 0:25 pass Soy 6.08 fail 0:26 pass The exemplary embodiments described herein are not intended to limit the invention or the scope of the appended claims. Various combinations and modifications of the embodiments described herein may be made without departing from the scope of the present disclosure and all modifications are meant to be included within the scope of the present disclosure. For instance, the various embodiments of the biodiesel treatments described herein may be used in conjunction with other embodiments of the biodiesel processing activities described herein. Further, the biodiesel treatment activities described herein may be implemented by modifying existing biodiesel processing systems and used in conjunction with existing biodiesel processing equipment. Thus, while certain exemplary embodiments and details have been described for purposes of exemplifying the invention, it will be apparent to those of ordinary skill in the art that various changes to the invention described herein may be made in any combination without departing from the scope of the present disclosure, which is defined in the appended claims.

Claims (118)

1. A process for treating biodiesel comprising:
placing biodiesel in contact with a compound capable of removing steryl glycosides from the biodiesel.
2. The process of claim 1, wherein the biodiesel contains at least 70 ppm of steryl glycosides before being placed in contact with the compound capable of removing steryl glycosides from the biodiesel.
3. The process of claim 1 or claim 2, wherein the biodiesel contains a greater amount of steryl glycosides before being placed in contact with the compound capable of removing steryl glycosides from the biodiesel than after being placed in contact with the compound capable of removing steryl glycosides from the biodiesel.
4. The process of any one of claims 1-3, wherein the compound capable of removing steryl glycosides from the biodiesel is selected from the group consisting of adsorbents, filter aids, boric acid, soap, sucrose, sugar, glucose, sodium chloride, citric acid, magnesium silicate, clay, diatomaceous earth, lecithin, granular clay, granular glucose, granular sugar, protein, textured vegetable protein, carbon, cellulose, solutions comprising boric acid, silica hydrogel, and combinations of any thereof.
5. The process of any one of claims 1-4, wherein the compound capable of removing steryl glycosides from the biodiesel is soluble in water.
6. The process of any one of claims 1-5, wherein the biodiesel is of a soy origin, a palm origin, or a combination thereof.
7. The process of any one of claims 1-6, further comprising separating the biodiesel from the compound capable of removing steryl glycosides from the biodiesel.
8. The process of any one of claims 1-7, wherein the biodiesel is placed in contact with the compound capable of removing steryl glycosides from the biodiesel at ambient room temperature.
9. The process of claim 7 or 8, further comprising mixing the biodiesel separated from the compound capable of removing steryl glycosides with a fuel selected from the group consisting of a petroleum based diesel fuel, a biodiesel not placed in contact the compound capable of removing steryl glycosides, ethanol, and any combinations thereof.
10. A product produced by the process of any one of claims 1-9.
11. A process for removing steryl glycosides from a fatty acid methyl ester containing material, comprising:
placing a compound selected from the group consisting of adsorbents, filter aids, boric acid, soap, sucrose, sugar, glucose, sodium chloride, citric acid, magnesium silicate, clay, diatomaceous earth, lecithin, granular clay, granular glucose, granular sugar, protein, textured vegetable protein, carbon, cellulose, solutions comprising boric acid, silica hydrogel, and combinations of any thereof in contact with a fatty acid containing material; and separating the compound from the fatty acid methyl ester containing material.
12. The process of claim 11, wherein the compound is separated from the fatty acid containing material by a process selected from the group consisting of filtration, centrifugation, and combinations of any thereof.
13. The process of claim 11 or claim 12, wherein the fatty acid containing material is selected from the group consisting of vegetable oil, canola oil, safflower oil, sunflower oil, nasturtium seed oil, mustard seed oil, olive oil, sesame oil, soybean oil, corn oil, peanut oil, cottonseed oil, rice bran oil, babassu nut oil, castor oil, palm oil, palm kernel oil, rapeseed oil, low erucic acid rapeseed oil, palm kernel oil, lupin oil, jatropha oil, coconut oil, flaxseed oil, evening primrose oil, jojoba oil, tallow, beef tallow, butter, chicken fat, lard, dairy butterfat, shea butter, biodiesel, used frying oil, oil miscella, used cooking oil, yellow trap grease, hydrogenated oils, derivatives of the oils, fractions of the oils, conjugated derivatives of the oils, and mixtures of any thereof.
14. A product produced by the process of any one of claims 11-13.
15. A process for reducing the filter blocking tendency of biodiesel, comprising:
placing the biodiesel in contact with a solid or liquid comprising a compound capable of reducing the filter blocking tendency of biodiesel.
16. The process of claim 15, wherein placing the biodiesel in contact with the solid or liquid comprises:
mixing the solid or liquid with the biodiesel; and separating the solid or liquid from the biodiesel.
17. The process of claim 15 or 16, wherein placing the biodiesel in contact with the solid or liquid comprises passing the biodiesel through a bed of the solid or the liquid.
18. The process of any one of claims 15-17, wherein steryl glycosides are removed from the biodiesel.
19. The process of any one of claims 15-18, wherein the solid or liquid is selected from the group consisting of adsorbents, filter aids, boric acid, soap, sucrose, sugar, glucose, sodium chloride, citric acid, magnesium silicate, clay, diatomaceous earth, lecithin, granular clay, granular glucose, granular sugar, protein, textured vegetable protein, carbon, cellulose, solutions comprising boric acid, silica hydrogel, beta-glucosidases, and combinations of any thereof.
20. A product produced by the process of any one of claims 15-19.
21. A process for producing biodiesel, comprising:
mixing a fatty acid containing material with an alcohol, thus producing a biodiesel precursor mixture;
subjecting the biodiesel precursor mixture to a condition selected from the group consisting of time, an increased temperature, an increased pressure, the presence of a catalyst and any combination thereof, thus producing biodiesel;
isolating the biodiesel; and removing steryl glycosides from the biodiesel at a temperature of less than 125°C.
22. The process of claim 21, wherein the fatty acid containing material is selected from the group consisting of vegetable oil, canola oil, safflower oil, sunflower oil, nasturtium seed oil, mustard seed oil, olive oil, sesame oil, soybean oil, corn oil, peanut oil, cottonseed oil, rice bran oil, babassu nut oil, castor oil, palm oil, palm kernel oil, rapeseed oil, low erucic acid rapeseed oil, palm kernel oil, lupin oil, jatropha oil, coconut oil, flaxseed oil, evening primrose oil, jojoba oil, tallow, beef tallow, butter, chicken fat, lard, dairy butterfat, shea butter, biodiesel, used frying oil, oil miscella, used cooking oil, yellow trap grease, hydrogenated oils, gums, soapstock, acid oil, derivatives of the oils, fractions of the oils, conjugated derivatives of the oils, and mixtures of any thereof.
23. The process of claim 21 or claim 22, wherein removing the steryl glycosides from the biodiesel comprises placing the biodiesel in contact with a compound capable of removing the steryl glycosides from the biodiesel.
24. The process of claim 23, wherein the compound capable of removing the steryl glycosides from the biodiesel is selected from the group consisting of adsorbents, filter aids, boric acid, soap, sucrose, sugar, glucose, sodium chloride, citric acid, magnesium silicate, clay, diatomaceous earth, lecithin, granular clay, granular glucose, granular sugar, protein, textured vegetable protein, carbon, cellulose, solutions comprising boric acid, silica hydrogel, and combinations of any thereof.
25. The process of any one of claims 21-24, wherein the fatty acid containing material is soy oil, palm oil or a combination thereof.
26. The process of any one of claims 21-25, further comprising transporting the biodiesel to a distribution facility.
27. The process of any one of claims 21-26, further comprising:
associating indicia indicating that the biodiesel is substantially free of the steryl glycosides, has a reduced tendency to block filters, passes a test that measures an ability of the biodiesel to block filters or any combination thereof with the biodiesel.
28. A product produced by the process of any one of claims 21-27.
29. A facility operatively configured to perform the process of any one of claims 1-9, 11-13, 15-19 and 21-27.
30. A biodiesel production plant comprising:
a compound capable of removing steryl glycosides from the biodiesel;
and a conduit operably configured to place biodiesel in contact with the compound capable of removing steryl glycosides from the biodiesel.
31. The biodiesel production plant of claim 30, further comprising a source of soy biodiesel, palm biodiesel or a combination thereof.
32. An apparatus configured to treat biodiesel, comprising:
a reservoir for containing an untreated biodiesel having an initial filter blocking tendency value;
a compound capable of removing steryl glycosides from the biodiesel;
and a conduit operatively configured to place the biodiesel in contact with the compound capable of removing steryl glycosides from the biodiesel.
33. The apparatus of claim 32, further comprising:
a device selected from the group consisting of a filter, a cyclone, a centrifuge, and combinations of any thereof;
wherein the device is configured to remove the compound capable of removing steryl glycosides from the biodiesel from the biodiesel.
34. The apparatus of claim 32 or 33, further comprising:
the untreated biodiesel within the reservoir; and treated biodiesel containing a lower amount of steryl glycosides as compared to the untreated biodiesel.
35. A method for reducing the filter blocking tendency of biodiesel, comprising:
obtaining a biodiesel having an initial filter blocking tendency value; and performing the process of any one of claims 1-9, 11-13, 15-19 and 20-27.
36. A process for preparing a composition enriched in steryl glycosides, comprising:
filtering a steryl glycoside containing composition through a bed of water-soluble solid bed material; and dissolving the water-soluble solid bed material in water to remove the water-soluble solid bed material, thus producing a composition enriched in steryl glycosides.
37. The process of claim 36, further comprising washing the bed with a solvent to remove solvent-soluble material.
38. The process of claim 36 or 37, wherein the steryl glycoside containing composition is biodiesel.
39. A product produced by the process of any one of claims 36-38.
40. A composition comprising steryl glycosides derived from biodiesel.
41. The composition of claim 40, wherein the steryl glycosides are purified.
42. The composition of claim 41, wherein the purified steryl glycosides are chemically modified.
43. The composition of claim 42, wherein the chemical modified steryl glycosides have at least one polyol added to the glycoside moiety of the steryl glycoside.
44. The composition of claim 42, wherein the chemically modified steryl glycosides have at least one carbohydrate added to the glycoside moiety of the steryl glycoside.
45. The process of any one of claims 1-9, 11-13, 15-19 and 20-27, further comprising:
isolating the steryl glycosides from biodiesel, isolating the steryl glycosides from the compound capable of removing the steryl glycosides from the biodiesel, or isolating the steryl glycosides from adsorbents, filter aids, boric acid, soap, sucrose, sugar, glucose, sodium chloride, citric acid, magnesium silicate, clay, diatomaceous earth, lecithin, granular clay, granular glucose, granular sugar, protein, textured vegetable protein, carbon, cellulose, solutions comprising boric acid, silica hydrogel, and combinations of any thereof.
46. A method of determining whether a biodiesel will be prone to blocking a filter, comprising:
obtaining a product produced by the process of any one of claims 1-9, 11-13, 15-19 and 20-27; and subjecting the product to a filter blocking test.
47. The method of claim 46, wherein the filter blocking test comprises:
determining whether a pre-selected volume of the product passes through a filter before a pre-selected pressure is placed on the filter from the product;
wherein the pre-selected volume of the product passes through the filter before the pre-selected pressure is reached, giving the biodiesel a passing test result;
wherein the pre-selected pressure is reached before the pre-selected volume of the product passes through the filter, giving the biodiesel a failing test result.
48. A biodiesel comprising a detectable level of steryl glycosides, wherein a level of steryl glycosides in the biodiesel is less than 70 ppm.
49. A biodiesel comprising:
a detectable level of steryl glycosides, diacylglycerols, or triacylglycerols;

and wherein the biodiesel passes a filter blocking test comprising:
determining whether a pre-selected volume of the product passes through a filter before a pre-selected pressure is placed on the filter from the product;
wherein the pre-selected volume of the product passes through the filter before the pre-selected pressure is reached, giving the biodiesel a passing test result;
wherein the pre-selected pressure is reached before the pre-selected volume of the product passes through the filter, giving the biodiesel a failing test result.
50. A biodiesel comprising:
a detectable level of steryl glycosides, diacylglycerols, or triacylglycerols;

and wherein the biodiesel passes a filter blocking test comprising:
adjusting a temperature of a sample of the biodiesel to 15 to 25 degrees Celsius;
shaking the sample vigorously for 120 seconds;
allowing the sample to stand on a vibration-free surface for 300 seconds;
placing 320 milliliters of the sample into a fuel reservoir beaker of a Normalab Analis NBF 240 instrument;
ensuring that the temperature of the sample is maintained at the 15 to 25 degrees Celsius;
placing a pump suction pipe of the Normalab Analis NBF 240 instrument into the fuel reservoir beaker;
operating a pump of the Normalab Analis NBF 240 instrument until biodiesel flows into a collection beaker;
pouring any fuel from the collection beaker into the fuel reservoir beaker;
placing a fresh filter on a filter unit of the Normalab Analis NBF
240 instrument;
attaching the assembled filter unit to the Normalab Analis NBF 240 instrument with a Luer fitting;
starting the pump of the Normalab Analis NBF 240 instrument;
reading a pressure gauge after 20 seconds; and pumping the sample until 300 milliliters have passed through the filter or until the pressure gauge reaches 105kPa;
wherein 300 milliliters of the sample passed through the filter before 105kPa was reached, giving the sample a passing test resuit;
wherein 105kPa was reached before 300 milliliters of the sample passed through the sample, giving the sample a failing test result.
51. The biodiesel of claim 49 or 50, wherein the biodiesel is of a soy origin, a palm origin, or a combination thereof.
52. The biodiesel of any one of claims 49-51, wherein the biodiesel comprises at least 0.4% monoglycerides.
53. The biodiesel of any one of claims 49-52, wherein the biodiesel comprises at least 0.1% diacylglycerols.
54. The biodiesel of any one of claims 49-53, wherein the biodiesel comprises at least 0.01% triacylglycerols.
55. A composition comprising:
the biodiesel of any one of claims 49-54; and a fuel selected from the group consisting of a petroleum based diesel, ethanol, a biodiesel having a detectable amount of steryl glycosides, and combinations of any thereof.
56. A process for treating biodiesel comprising:
placing biodiesel in contact with a compound selected from the group consisting of adsorbents, filter aids, boric acid, soap, sucrose, sugar, glucose, sodium chloride, citric acid, magnesium silicate, clay, diatomaceous earth, lecithin, granular clay, granular glucose, granular sugar, protein, textured vegetable protein, carbon, cellulose, solutions comprising boric acid, silica hydrogel, and combinations of any thereof; and separating the biodiesel from the compound.
57. A process for treating biodiesel comprising:
placing biodiesel in contact with a compound capable of removing monoacylglycerols from the biodiesel.
58. The process of claim 57, wherein the biodiesel contains at least 0.7% of the monoacylglycerols before being placed in contact with the compound capable of removing the monoacylglycerols from the biodiesel.
59. The process of claim 57 or claim 58, wherein the biodiesel contains a greater amount of the monoacylglycerols before being placed in contact with the compound capable of removing the monoacylglycerols from the biodiesel than after being placed in contact with the compound capable of removing the monoacylglycerols from the biodiesel.
60. The process of any one of claims 57-59, wherein the compound capable of removing the monoacylglycerols from the biodiesel is selected from the group consisting of magnesium silicate, steryl glycosides and a combination thereof.
61. The process of any one of claims 57-60, wherein the biodiesel is of a soy origin, a palm origin or a combination thereof.
62. The process of any one of claims 57-61, further comprising separating the biodiesel from the compound capable of removing the monoacylglycerols from the biodiesel.
63. The process of any one of claims 57-62, wherein the biodiesel is placed in contact with the compound capable of removing the monoacylglycerols from the biodiesel at ambient room temperature.
64. The process of claim 62 or 63, further comprising mixing the biodiesel separated from the compound capable of removing the monoacylglycerols with a fuel selected from the group consisting of a petroleum based diesel fuel, a biodiesel not placed in contact the compound capable of removing the monoacylglycerols, ethanol, and any combinations thereof.
65. A product produced by the process of any one of claims 57-64.
66. A process for removing monoacylglycerols from a fatty acid methyl ester containing material, comprising:
placing a compound selected from the group consisting of magnesium silicate, granular sugar, steryl glycosides, and any combination thereof in contact with a fatty acid containing material; and separating the compound from the fatty acid containing material.
67. The process of claim 66, wherein the compound is separated from the fatty a cid containing material by a process selected from the group consisting of filtration, centrifugation, and combinations of any thereof.
68. The process of claim 66 or claim 67, wherein the fatty acid containing material is selected from the group consisting of vegetable oil, canola oil, safflower oil, sunflower oil, nasturtium seed oil, mustard seed oil, olive oil, sesame oil, soybean oil, corn oil, peanut oil, cottonseed oil, rice bran oil, babassu nut oil, castor oil, palm oil, palm kernel oil, rapeseed oil, low erucic acid rapeseed oil, lupin oil, jatropha oil, coconut oil, flaxseed oil, evening primrose oil, jojoba oil, camelina oil, tallow, beef tallow, butter, chicken fat, lard, dairy butterfat, shea butter, biodiesel, used frying oil, oil miscella, used cooking oil, yellow trap grease, hydrogenated oils, derivatives of the oils, fractions of the oils, conjugated derivatives of the oils, and mixtures of any thereof.
69. A product produced by the process of any one of claims 66-68.
70. A process for reducing the filter blocking tendency of biodiesel, comprising:
placing the biodiesel in contact with a solid or liquid comprising a compound capable of reducing the filter blocking tendency of biodiesel.
71. The process of claim 70, wherein placing the biodiesel in contact with the solid comprises:
mixing the solid with the biodiesel; and separating the solid from the biodiesel.
72. The process of claim 70 or claim 71, wherein placing the biodiesel in contact with the solid comprises passing the biodiesel through a bed of the solid.
73. The process of any one of claims 70-72, wherein placing the biodiesel in contact with the solid or the liquid removes the monoacylglycerols from the biodiesel.
74. A product produced by the process of any one of claims 70-73.
75. A process for producing biodiesel, comprising:
mixing a fatty acid containing material with an alcohol, thus producing a biodiesel precursor mixture;
subjecting the biodiesel precursor mixture to a condition that allows biodiesel to form, the condition being selected from the group consisting of time, an increased temperature, an increased pressure, the presence of a catalyst and any combinations thereof;
isolating the biodiesel; and removing monoacylglycerols from the biodiesel at a temperature of less than 125°C.
76. The process of claim 75, wherein the fatty acid containing material is selected from the group consisting of vegetable oil, canola oil, safflower oil, sunflower oil, nasturtium seed oil, mustard seed oil, olive oil, sesame oil, soybean oil, corn oil, peanut oil, cottonseed oil, rice bran oil, babassu nut oil, castor oil, palm oil, palm kernel oil, rapeseed oil, low erucic acid rapeseed oil, palm kernel oil, lupin oil, jatropha oil, coconut oil, flaxseed oil, evening primrose oil, jojoba oil, camelina oil, tallow, beef tallow, butter, chicken fat, lard, dairy butterfat, shea butter, biodiesel, used frying oil, oil miscelia, used cooking oil, yellow trap grease, hydrogenated oils, gums, soapstock, acid oil, derivatives of the oils, fractions of the oils, conjugated derivatives of the oils, and mixtures of any thereof.
77. The process of claim 75 or claim 76, wherein removing the monoacylglycerols from the biodiesel comprises placing the biodiesel in contact with a compound capable of removing the monoacylglycerols from the biodiesel.
78. The process of claim 77, wherein the compound capable of removing the monoacylglycerols from the biodiesel is magnesium silicate.
79. The process of any one of claims 74-78, wherein the fatty acid containing material is soy oil, palm oil or a combination thereof.
80. The process of any one of claims 74-79, further comprising transporting the biodiesel to a distribution facility.
81. The process of any one of claims 74-80, further comprising:
associating indicia with the biodiesel, the indicia indicating that the biodiesel has a reduced content of monoacylglycerols.
82. A product produced by the process of any one of claims 74-81.
83. A facility operatively configured to perform the process of any one of claims 57-64, 66-68, 70-73 and 75-82.
84. A biodiesel production plant comprising:
a compound capable of removing monoacylglycerols from the biodiesel;
and a conduit operably configured to place biodiesel in contact with the compound capable of removing the monoacylglycerols from the biodiesel.
85. The biodiesel production plant of claim 84, further comprising a source of soy biodiesel, palm biodiesel or a combination thereof.
86. A system configured to treat biodiesel, comprising:
a reservoir for containing a biodiesel having an initial filter blocking tendency value;
a compound capable of removing monoacylglycerols from the biodiesel;
and a conduit operatively configured to place the biodiesel in contact with the compound capable of removing the monoacylglycerols from the biodiesel.
87. The system of claim 86, further comprising:
a device selected from the group consisting of a filter, a cyclone, a centrifuge, and any combinations thereof, the device being configured to remove the compound capable of removing the monoacylglycerols from the biodiesel from the biodiesel.
88. The apparatus of claim 86 or claim 87, further comprising:
the biodiesel having the initial filter blocking tendency value within the reservoir; and treated biodiesel containing a lower amount of the monoacylglycerols as compared to the biodiesel having the initial filter blocking tendency value.
89. A process for treating biodiesel comprising:
placing biodiesel in contact with magnesium silicate; and separating the biodiesel from the magnesium silicate.
90. The process according to claim 89, further comprising placing biodiesel in contact with a compound capable of removing steryl glycosides from the biodiesel.
91. A process for treating biodiesel, comprising:
placing biodiesel in contact with a solid or liquid capable of improving the result of a cold test of biodiesel.
92. The process of claim 91, wherein placing the biodiesel in contact with the solid or the liquid comprises:
mixing the solid or the liquid with the biodiesel at a first temperature;
separating the solid or the liquid from the biodiesel;
adjusting the biodiesel to have a second temperature; and subjecting the biodiesel to a cold test.
93. A process for reducing saturated fatty acid esters in biodiesel comprising:
adjusting a temperature of the biodiesel;
mixing a solid capable of reducing the content of monoacylglycerols in the biodiesel with the biodiesel; and separating the solid from the biodiesel.
94. A process for reducing monoacylglycerols in biodiesel comprising;
mixing a solid capable of reducing the content of monoacylglycerols in the biodiesel with the biodiesel; and separating the solid from the biodiesel.
95. The process of claim 94, further comprising adjusting the temperature of the biodiesel to 60 °C.
96. A process for treating biodiesel, comprising:
placing the biodiesel in contact with a liquid capable of improving the result of a filter blocking test of biodiesel.
97. The process of claim 96, wherein the liquid comprises a solvent.
98. A process for improving the filter blocking tendency of a blend of biodiesel and petroleum diesel, comprising:
placing the biodiesel in contact with a compound capable of reducing the filter blocking tendency of the biodiesel, thus producing treated biodiesel;
and blending petroleum diesel with the treated biodiesel such that the blend of the biodiesel and the petroleum diesel has a reduced filter blocking tendency as compared to a blend of petroleum diesel and biodiesel that has not been placed in contact with the compound capable of reducing the filter blocking tendency of the biodiesel.
99. A process for improving the filter blocking tendency of a blend of biodiesel and petroleum diesel, comprising:
blending petroleum diesel with biodiesel, thus producing a blend of petroleum diesel and biodiesel;
placing the blend in contact with a compound capable of reducing the filter blocking tendency of the blend, thus producing a treated blend of petroleum diesel and biodiesel;
wherein the treated blend has a reduced filter blocking tendency as compared to the blend of the petroleum diesel and the biodiesel that has not been placed in contact with the compound capable of reducing the filter blocking tendency of the blend.
100. A process of purifying steryl glycosides from biodiesel, comprising:
incubating a compound selected from the group consisting of biodiesel, filter cake from biodiesel production, final filter cake, and combinations of any thereof with a first solvent, thus producing a solid component and a liquid component;
separating the solid component from the liquid component;
washing the solid component with a second solvent; and removing the second solvent from the first solvent, thus producing a purified steryl glycoside.
101. A process for improving filter blocking tendency of biodiesel, comprising;
filtering biodiesel through a filter aid selected from the group consisting of diatomaceous earth, sugar and a combination thereof.
102. The process of claim 101, further comprising incubating the biodiesel.
103. The process of claim 101, wherein the biodiesel is incubated at 40°F.
104. A process for improving filter blocking tendency of biodiesel, comprising placing biodiesel in contact with carbon.
105. The process of claim 104, further comprising separating the carbon from the biodiesel.
106. The process of claim 105, further comprising incubating the biodiesel at 70°F.
107. The process of claim 106, further comprising filtering the biodiesel through diatomaceous earth.
108. The process of any one of claims 102 or 104-107, wherein the steryl glycoside content of biodiesel is decreased after filtration.
109. The process of claim 15, wherein the filter blocking test comprises:
determining whether a pre-selected volume of the product passes through a filter within a pre-selected time;
wherein the pre-selected volume of the product passes through the filter before the pre-selected time is reached, giving the product a passing test result;
wherein the pre-selected time is reached before the pre-selected volume of the product passes through the filter, giving the product a failing test result.
110. The process of claim 15, further comprising subjecting the biodiesel to a degumming step.
111. The process of claim 15, further comprising;
incubating biodiesel at a temperature between 40°F and 70 °F;
and filtering the incubated biodiesel, thus obtaining filtered biodiesel.
112. The process of claim 111, wherein the incubated biodiesel is filtered through a compound selected from the group consisting of diatomaceous earth, carbon, cellulose, and combinations of any thereof.
113. The process of claim 112, wherein the compound is contacted with the biodiesel as a body feed.
114. The process of claim 112, further comprising forming a precoat of the compound on a filter.
115. The process of any of claims 111-114, further comprising subjecting filtered biodiesel to a test selected from the group consisting of ASTM
D2068, a modified ASTM D6217 and a combination thereof.
116. The process of claim 115, further comprising incubating the filtered biodiesel for a second incubation period prior to subjecting the filtered biodiesel to the test, thus decreasing the content of steryl glycosides in the filtered biodiesel.
117. A biodiesel comprising:
a detectable level of steryl glycosides, diacylglycerols, triacylglycerols or any combination thereof;
wherein the biodiesel passes a test in less than six minutes, the test comprising filtering a volume of 300 ml of biodiesel through a 1.6 um GF/A
filter having 47 mm diameter under a 21-25 inch Hg vacuum.
118. A process for producing biodiesel, comprising:
mixing a fatty acid containing material with an alcohol, thus producing a biodiesel precursor mixture;
subjecting the biodiesel precursor mixture to a condition that allows biodiesel to form, the condition being selected from the group consisting of time, an increased temperature, an increased pressure, the presence of a catalyst and any combinations thereof;
isolating the biodiesel; and treating the biodiesel with silica hydrogel.
CA002629121A 2005-12-29 2006-12-29 Processes of producing biodiesel and biodiesel produced therefrom Abandoned CA2629121A1 (en)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US75497905P 2005-12-29 2005-12-29
US60/754,979 2005-12-29
US83157506P 2006-07-17 2006-07-17
US60/831,575 2006-07-17
US11/614,618 US20070151146A1 (en) 2005-12-29 2006-12-21 Processes of Producing Biodiesel and Biodiesel Produced Therefrom
US11/614,618 2006-12-21
PCT/US2006/049680 WO2007076163A2 (en) 2005-12-29 2006-12-29 Biodiesel production processes and biodiesel produced therefrom

Publications (1)

Publication Number Publication Date
CA2629121A1 true CA2629121A1 (en) 2007-07-05

Family

ID=38218738

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002629121A Abandoned CA2629121A1 (en) 2005-12-29 2006-12-29 Processes of producing biodiesel and biodiesel produced therefrom

Country Status (7)

Country Link
US (1) US20070151146A1 (en)
EP (1) EP1969090A2 (en)
AU (1) AU2006330770A1 (en)
BR (1) BRPI0620595A2 (en)
CA (1) CA2629121A1 (en)
MX (1) MX2008008246A (en)
WO (1) WO2007076163A2 (en)

Families Citing this family (66)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9109170B2 (en) * 2006-02-02 2015-08-18 Reg Biofuels, Llc Biodiesel cold filtration process
CL2007000734A1 (en) * 2006-03-22 2008-05-02 Grace W R & Co TRANSPARENT INORGANIC OXIDE COATING PRODUCED WHEN PREPARING COMPOSITION OF COATING, INCLUDING INORGANIC AND POLYMER OXIDE PARTICLES, APPLY SUBSTRATE COMPOSITION, FORM COATING AND HEATING COATING FOR ELIMI
US20080034646A1 (en) * 2006-08-08 2008-02-14 Chesapeake Green Fuel Deproteination of fats and oils and refining of triglycerides
WO2008055676A1 (en) * 2006-11-07 2008-05-15 Süd-Chemie AG Method for purification of biodiesel
EP1920829A1 (en) 2006-11-07 2008-05-14 Süd-Chemie Ag Amorphous adsorbent, method of obtaining the same and its use in the bleaching of fats and/or oils
US20080115407A1 (en) * 2006-11-22 2008-05-22 Hoffman Mark A System and method for producing biodiesel
US20080282606A1 (en) * 2007-04-16 2008-11-20 Plaza John P System and process for producing biodiesel
KR20100067111A (en) 2007-09-12 2010-06-18 마텍 바이오싸이언스스 코포레이션 Biological oils and production and uses thereof
DE102007059620A1 (en) * 2007-12-12 2009-06-18 Bundesrepublik Deutschland, vertreten durch den Präsidenten der Bundesanstalt für Geowissenschaften und Rohstoffe Purification of biodiesel using allophane and / or imogolite
GB0725194D0 (en) * 2007-12-24 2008-01-30 Desmet Ballestra Engineering S Process for producing biodiesel with improved filtration characteristics and biodiesel thus produced
JP2009155476A (en) * 2007-12-26 2009-07-16 Nippon Shokubai Co Ltd Method and apparatus for producing fatty acid alkyl ester and/or glycerin
US8097049B2 (en) * 2008-02-07 2012-01-17 The Dallas Group Of America, Inc. Biodiesel purification by a continuous regenerable adsorbent process
EP2098585A1 (en) * 2008-02-28 2009-09-09 Süd-Chemie Ag Method for purifying biodiesel or biodiesel precursors
WO2009132670A1 (en) * 2008-04-30 2009-11-05 Süd-Chemie AG Process for removing steryl glycosides from biodiesel
GB0812559D0 (en) * 2008-07-09 2008-08-13 Danisco Method
EP2331658B1 (en) * 2008-08-05 2019-06-26 Spirit Of The 21st Century Group, LLC Modified fuels
DE102008050935B4 (en) 2008-10-10 2015-07-09 Air Liquide Global E&C Solutions Germany Gmbh Process and installation for the separation of steryl glycosides in biodiesel production
DE102008058393A1 (en) 2008-11-21 2010-05-27 Süd-Chemie AG Alumina-containing adsorbents for the purification of biodiesel
DK2352712T3 (en) 2008-11-26 2018-09-10 Elevance Renewable Sciences PROCEDURES FOR PREPARING JET FUEL FROM NATURAL OIL MATERIALS THROUGH METATES REACTIONS
CN102227489B (en) * 2008-11-26 2015-04-15 埃莱文斯可更新科学公司 Methods of producing jet fuel from natural oil feedstocks through oxygen-cleaved reactions
US20150267145A1 (en) * 2008-12-08 2015-09-24 Initio Fuels, Llc Single step transesterification of biodiesel feedstock using a gaseous catalyst
AU2009333542A1 (en) * 2008-12-08 2011-07-28 Initio Fuels Llc Single step transesterification of feedstock using a gaseous catalyst
DE102009006921A1 (en) 2009-02-02 2010-08-05 Lurgi Gmbh Producing fatty acid alkyl esters comprises transesterification of fats or oils with alkyl alcohols, where the fats or oils, the alkyl alcohols and a catalyst are separated into a light, ester-rich phase and a heavy, glycerin-rich phase
DE102009006920B4 (en) 2009-02-02 2016-03-17 Air Liquide Global E&C Solutions Germany Gmbh A method for preventing sterol glycoside-containing precipitates in the production of fatty acid alkyl esters
DE102009006919A1 (en) 2009-02-02 2010-08-05 Lurgi Gmbh Producing fatty acid alkyl ester comprises e.g. mixing fats or oils, alkyl alcohols and catalyst, separating mixture into low, ester-rich phase and heavy glycerin-rich phase, and separating fatty acid alkyl ester from low, ester-rich phase
DE102009006922A1 (en) 2009-02-02 2010-08-05 Lurgi Gmbh Making fatty acid alkyl ester by transesterifying fats or oils with alkyl alcohol and a catalyst, comprises mixing fats or oils, alkyl alcohol and catalyst and separating fatty acid alkyl esters from a light and ester-rich phase and drying
DE102009006923A1 (en) 2009-02-02 2010-08-05 Lurgi Gmbh Removing sterol glycoside containing precipitates in production of fatty acid alkyl esters comprises mixing fats or oils, alkyl and catalyst, and separating mixture into light phase, ester rich phase and heavy, glycerin rich phase
GB0902009D0 (en) 2009-02-09 2009-03-11 Innospec Ltd Improvements in fuels
JP5378001B2 (en) * 2009-02-17 2013-12-25 花王株式会社 Method for purifying fatty acid alkyl ester
EP2406362A1 (en) 2009-03-09 2012-01-18 Novozymes A/S Enzymatic removal of steryl glycosides in fatty acid alkyl esters
JP5618648B2 (en) * 2009-06-30 2014-11-05 花王株式会社 Process for producing fatty acid lower alkyl ester, glycerin and steryl glucoside
US9382502B2 (en) 2009-10-12 2016-07-05 Elevance Renewable Sciences, Inc. Methods of refining and producing isomerized fatty acid esters and fatty acids from natural oil feedstocks
US9169447B2 (en) 2009-10-12 2015-10-27 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US8735640B2 (en) 2009-10-12 2014-05-27 Elevance Renewable Sciences, Inc. Methods of refining and producing fuel and specialty chemicals from natural oil feedstocks
US9365487B2 (en) 2009-10-12 2016-06-14 Elevance Renewable Sciences, Inc. Methods of refining and producing dibasic esters and acids from natural oil feedstocks
US9222056B2 (en) 2009-10-12 2015-12-29 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US9051519B2 (en) 2009-10-12 2015-06-09 Elevance Renewable Sciences, Inc. Diene-selective hydrogenation of metathesis derived olefins and unsaturated esters
US9000246B2 (en) 2009-10-12 2015-04-07 Elevance Renewable Sciences, Inc. Methods of refining and producing dibasic esters and acids from natural oil feedstocks
CA2777265C (en) 2009-10-12 2019-04-16 Elevance Renewable Sciences, Inc. Methods of refining and producing fuel from natural oil feedstocks
US9175231B2 (en) 2009-10-12 2015-11-03 Elevance Renewable Sciences, Inc. Methods of refining natural oils and methods of producing fuel compositions
WO2011072245A1 (en) * 2009-12-11 2011-06-16 Envirosource, Inc. Systems and methods for processing glycerol
EP2519625B1 (en) 2009-12-28 2018-09-26 DSM IP Assets B.V. Recombinant thraustochytrids that grow on sucrose, and compositions, methods of making, and uses thereof
EP2526147B1 (en) 2010-01-22 2019-06-19 Archer-Daniels-Midland Company Polyvinyl halide composition containing renewable source-based plasticizers
US20110192076A1 (en) * 2010-02-05 2011-08-11 Evonik Rohmax Additives Gmbh Composition having improved filterability
WO2011109945A1 (en) * 2010-03-08 2011-09-15 中山大学 Biodiesel and preparation method thereof
BR112012025043A2 (en) * 2010-04-02 2018-07-24 Envirosource Inc system and methods for processing glycerol
DE102010022139A1 (en) 2010-05-20 2011-11-24 Lurgi Gmbh Process for the production of biodiesel
FR2962434B1 (en) 2010-07-08 2013-09-06 Arkema France PROCESS FOR THE PURIFICATION OF AN ALKYL ESTER OF FATTY ACID BY LIQUID / LIQUID EXTRACTION
EP2447342A1 (en) 2010-10-26 2012-05-02 Süd-Chemie AG Method for Biodiesel and Biodiesel Precursor Production
SE535398C2 (en) * 2011-01-21 2012-07-24 Perstorp Ab Process for the purification of biodiesel with self-cleaning filters
WO2012177348A1 (en) * 2011-06-21 2012-12-27 W. R. Grace & Co.-Conn. Catalytic purification of fatty acid alkyl esters used in fuels
US9133416B2 (en) 2011-12-22 2015-09-15 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US9139493B2 (en) 2011-12-22 2015-09-22 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US9169174B2 (en) 2011-12-22 2015-10-27 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US20140047762A1 (en) * 2012-07-09 2014-02-20 Real Technologies Llc Fuel additive and method for use
AR091994A1 (en) 2012-03-16 2015-03-18 Keclon S A STERILE GLYCOSID REMOVAL METHOD
WO2013184746A1 (en) 2012-06-08 2013-12-12 A.L.M Holding Company Biodiesel emulsion for cleaning bituminous coated equipment
US9388098B2 (en) 2012-10-09 2016-07-12 Elevance Renewable Sciences, Inc. Methods of making high-weight esters, acids, and derivatives thereof
US9701916B2 (en) 2013-10-18 2017-07-11 National Institute Of Advanced Industrial Science And Technology Method for producing high quality biodiesel fuel
WO2015100063A1 (en) 2013-12-26 2015-07-02 Exxonmobil Research And Engineering Company Methods of inhibiting precipitation of biodiesel fuel components
WO2017040210A1 (en) * 2015-08-28 2017-03-09 Imerys Filtration Minerals, Inc. High permeability composite magnesium silicate filter aids
EP3389817B1 (en) * 2015-12-15 2023-06-21 Donaldson Company, Inc. Liquid hydrocarbon filterability system
BR102016023104B1 (en) 2016-10-04 2021-08-31 Petróleo Brasileiro S.A. - Petrobras Biodiesel purification process
EP3404082A1 (en) 2017-05-19 2018-11-21 GEA Mechanical Equipment GmbH Method for reducing the volume of monoglycerides (mg), in particular saturated monoglycerides (gmg), in a raw biodiesel
WO2019032521A1 (en) * 2017-08-10 2019-02-14 Archer Daniels Midland Company Processes of producing biodiesel and biodiesel produced therefrom
CN112461705A (en) * 2021-01-21 2021-03-09 江苏曼氏生物科技股份有限公司 Method for detecting sterol glycoside content in refined medicinal soybean phospholipid

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US225375A (en) * 1880-03-09 Corset-steel fastening
US2225375A (en) * 1938-10-03 1940-12-17 Purdure Res Foundation Process of obtaining sterol glucosides and sterols from fatty substances
JPS5329912A (en) * 1976-08-31 1978-03-20 Nippon Shinyaku Co Ltd Preparation of sterol-glycosides from vegetable material
US4681768A (en) * 1985-08-14 1987-07-21 Reagent Chemical & Research Company Treatment of cooking oils and fats
US5597600A (en) * 1995-06-05 1997-01-28 The Dallas Group Of America, Inc. Treatment of cooking oils and fats with magnesium silicate and alkali materials
US5972057A (en) * 1997-11-11 1999-10-26 Lonford Development Limited Method and apparatus for producing diesel fuel oil from waste edible oil
DE10038442A1 (en) * 2000-08-07 2002-02-21 Cognis Deutschland Gmbh Process for obtaining sterols from residues containing fatty acids
WO2003022064A1 (en) * 2001-09-07 2003-03-20 Cargill Incorporated Steryl ester compositions
US7199084B2 (en) * 2002-03-21 2007-04-03 Schlumberger Technology Corporation Concentrated suspensions
DE602004024430D1 (en) * 2003-10-09 2010-01-14 Dallas Group America Inc CLEANING BIODIESEL WITH ADSORPTION SUBSTANCES
DE10353150A1 (en) * 2003-11-14 2005-06-16 Cognis Deutschland Gmbh & Co. Kg Process for the simultaneous production of sterols and polar lipids
MY173044A (en) * 2003-11-19 2019-12-20 Carotech Bhd Recovery of phytonutriens from oils
CA2599499A1 (en) * 2005-02-28 2006-08-31 University Of Ottawa Apparatus and method for bio-fuel production
US20060236598A1 (en) * 2005-04-26 2006-10-26 Flint Hills Resources, L.P. Low temperature biodiesel diesel blend
US20060260184A1 (en) * 2005-05-20 2006-11-23 Mbp Bioenergy, Llc Apparatus and process for the refinement of biodiesel fuel
US9109170B2 (en) * 2006-02-02 2015-08-18 Reg Biofuels, Llc Biodiesel cold filtration process
WO2008051984A2 (en) * 2006-10-23 2008-05-02 Blue Sun Biodiesel, Llc Methods of purifying biodiesel fuels

Also Published As

Publication number Publication date
WO2007076163A2 (en) 2007-07-05
EP1969090A2 (en) 2008-09-17
AU2006330770A1 (en) 2007-07-05
US20070151146A1 (en) 2007-07-05
BRPI0620595A2 (en) 2011-11-16
WO2007076163A3 (en) 2008-04-03
MX2008008246A (en) 2008-09-11

Similar Documents

Publication Publication Date Title
CA2629121A1 (en) Processes of producing biodiesel and biodiesel produced therefrom
CA2576750C (en) Biodiesel cold filtration process
CN105916969B (en) Removal of free fatty acids from glyceride oils
CN106350217B (en) A kind of preparation method of low cloud point fatty acid type diesel antiwear additive
EP2114851B1 (en) Process for separating saturated and unsaturated fatty acids
SK279266B6 (en) Method of refining oils containing glycerides
KR20100114017A (en) Purification treatment of fatty materials
CN102504950B (en) Method for decolorizing tea seed oil
JP4197357B1 (en) Oil and fat separation method
Saeong et al. The response surface optimization of steryl glucosides removal in palm biodiesel using silica adsorption
WO2019032521A1 (en) Processes of producing biodiesel and biodiesel produced therefrom
CN101481634A (en) Lubricity additives and methods of producing lubricity additives
US8545702B1 (en) Production of biodiesel from feedstock
US9238785B2 (en) Method for biodiesel and biodiesel precursor production
WO2007146971A1 (en) Method of refining oil recovered from ethanol processing byproducts
US8629291B1 (en) Esterification of biodiesel feedstock with solid heterogeneous catalyst
GB2466493A (en) Process for the production and treatment of biodiesel with improved cold soak test results
US20200199471A1 (en) Method for Reducing the Content of Saturated Monoglycerides in a Raw Biodiesel
EP2361150A1 (en) Aluminum oxide-containing adsorbents for the purification of biodiesel
EP4299174A1 (en) Adsorbent composition with improved filtration behavior
WO2012099523A1 (en) Method for purification of biodiesel using a self-cleaning filter
WO2010010952A1 (en) Cloud point depressant for fatty acid alkyl ester
JP5301982B2 (en) Process for producing concentrated phorbol ester
WO2011004897A1 (en) Raw oil or fat for production of higher fatty acid alkyl ester, and process for production of higher fatty acid alkyl ester
PL241180B1 (en) Innovative method of obtaining modified fat

Legal Events

Date Code Title Description
EEER Examination request
FZDE Discontinued

Effective date: 20121113