EP0059669A2 - Purification of sugar liquors with activated carbon - Google Patents

Purification of sugar liquors with activated carbon Download PDF

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Publication number
EP0059669A2
EP0059669A2 EP82400341A EP82400341A EP0059669A2 EP 0059669 A2 EP0059669 A2 EP 0059669A2 EP 82400341 A EP82400341 A EP 82400341A EP 82400341 A EP82400341 A EP 82400341A EP 0059669 A2 EP0059669 A2 EP 0059669A2
Authority
EP
European Patent Office
Prior art keywords
activated carbon
purification
sugar
sugar liquors
dextrose
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.)
Withdrawn
Application number
EP82400341A
Other languages
German (de)
French (fr)
Other versions
EP0059669A3 (en
Inventor
John E. Urbanic
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.)
Calgon Corp
Original Assignee
Calgon Corp
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 Calgon Corp filed Critical Calgon Corp
Publication of EP0059669A2 publication Critical patent/EP0059669A2/en
Publication of EP0059669A3 publication Critical patent/EP0059669A3/en
Withdrawn legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C13SUGAR INDUSTRY
    • C13BPRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
    • C13B20/00Purification of sugar juices
    • C13B20/12Purification of sugar juices using adsorption agents, e.g. active carbon
    • C13B20/123Inorganic agents, e.g. active carbon
    • CCHEMISTRY; METALLURGY
    • C13SUGAR INDUSTRY
    • C13KSACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
    • C13K1/00Glucose; Glucose-containing syrups
    • C13K1/06Glucose; Glucose-containing syrups obtained by saccharification of starch or raw materials containing starch
    • C13K1/08Purifying

Definitions

  • This invention is directed to a method of purification and decolorization of sugar liquors.
  • This invention especially relates to an improved method for the purification and decolorization of sugar liquors including starch hydrolyzates such as corn syrup.
  • this invention provides for a purification of sugar liquors through the use of a special granular activated carbon resulting in final products of high purity.
  • starch hydrolyzate includes solutions of starch hydrolyzate which contain a mixture of mono-, di-, and higher polysaccharides and it particularly includes sugar solutions derived from cane, beet and corn sources.
  • oligosaccharide as used herein, is a carbohydrate containing from 2 to 8 simple sugars linked together. Combinations of more than 8 simple sugars are polysaccharides.
  • a starch hydrolyzate is defined as an aqueous mixture of sugar components derived from acid, enzyme or other treatment of starchy materials.
  • sugar liquors such as corn syrup
  • cane sugar and relatively impure solutions of dextrose is one of the oldest established industrial chemical procedures.
  • Aqueous solutions of certain sugars such as glucose occur industrially in the hydrolysis of amylaceous or cellulosic materials.
  • large quantities of glucose solutions are prepared by the hydrolysis of starch in the manufacture of corn syrup, corn sugar and dextrose. These solutions contain minor but significant amounts of other sugars not removed by conventional refining procedures.
  • activated carbon is the decolorization of sugar liquors.
  • the powdered activated carbon is slurried with the impure liquor one or more times followed by filtration of the decolorized liquor.
  • Decolorization is also accomplished by passing the liquors through a column of granular activated carbon. These procedures remove color-causing impurities but only incidental amounts of oligosaccharides present in the liquor.
  • activated carbon involves the adsorption of high molecular weight sugars in addition to color causing impurities.
  • Activated carbon has been employed in a column chromatography system for removing such impurities from a glucose solution as described in U.S. Patent No. 2,549,840.
  • Cakes of powdered activated carbon have been used in a series of filters to accomplish the removal of impurities from sugar liquors as described in U.S. Patent No. 3,551,203.
  • the object of this invention is directed to an improved method for the purification of sugar liquors.
  • a special granular activated carbon which due to its high iodine number and large average particle size allows for a reduction in the amount of activated carbon necessary and for an increased flow rate through a carbon filter process such as described above.
  • This invention allows the use of high flow rates with the benefit of increased yield of purified sugar product over the prior art. This high yield reduces both capital and operating cost for processes to remove oligosaccharides and polysaccharides from impure sugar liquors.
  • an improvement in the method of purifying and decolorizing sugar liquors which includes contacting said sugar liquors with a sufficient amount of activated carbon to adsorb oligosaccharides containing 3 or more saccharide groups. Said contact is maintained for a period of time sufficient to accomplish substantially complete adsorption of said oligosaccharides.
  • the improvement comprises the use of granular activated carbon with an iodine number of at least 1,000, preferably at least 1,200 and an'average particle size in the range of 0.4 mm to 4.0 0 mm.
  • the activated carbon employed in this improved method must have an iodine number of at least 1,000 and an average particle size in the range of 0.4 mm to 4.0 mm.
  • Typical prior art activated carbons for use in sugar purification have had iodine numbers below 500.
  • the iodine number is useful in quantifying the adsorbtive capacity of the activated carbon.
  • the iodine number is defined as the milligrams of iodine adsorbed from an aqueous idodine-potassium iodine solution by one gram of activated carbon when the iodine concentration of the residual filtrate is 0.02 normal.
  • a corn syrup solution by definition is a dextrose hydrolyzate of less than 99% dextrose.
  • Dextrose, or D(+)-glucose has a variety of uses especially in its pure form. For example, dextrose with no impurities would give an excellent product to breweries for beer fermentation. The higher molecular weight sugars present in dextrose hydrolyzate, if not removed, would contribute to an increased caloric content of the final beer. High purity dextrose would also be an advantage in the production of sorbitol where the oligosaccharides of 3 or more sugars interfere with hydrogenation.
  • DP-n refers to the degree of polymerization where n is the number of sugar units in the polymer.
  • the dextrose hydrolyzate syrup to be purified can be treated as an aqueous solution of from 18.5 to 30.0% dry substance.
  • the range is dependent on preventing decomposition of the liquor and on keeping the viscosity at a reasonable, i.e., workable level.
  • the purification of the hydrolyzate solution is accomplished by passing the solution through a series of columns, containing granular activated carbon with an iodine number of at least 1,000 and with an average particle size in the range of 0.4 mm to 4.0 mm at a flow rate in a range of 1 to 3 gpm/ft. cross sectional area generating a contact time in each column in a range of about 10 to 30 minutes.
  • a starch hydrolyzate comprised of 97% dextrose, 2.4% DP-2, 0.2% DP-3 and 0.4% DP-4 was purified on a series of eight, four foot by one inch (i.d.) columns each loaded with 255 grams (600 cc) of granular activated carbon with an iodine number in the range of 1,000 to 1,050 and an average particle size in the range of 0.9 mm to 1.5 mm, at a flow rate of 20.8 ml/min. generating a contact time in each column of about 30 minutes.
  • the yield of purified dextrose (98.5% dextrose - 1.5% DP-2) ) was between 20-25 grams per gram of activated carbon.
  • the starch hydrolyzate of Example 1 was purified through the series of columns of Example 1 loaded with granular activated carbon with an iodine number in the range of 1,200 to 1,400 and an average particle size in the range of 0.9 mm to 1.5 mm at a flow rate of 20.8 ml/min. generating a contact time in each column of about 30 minutes.
  • the yield of purified dextrose was between 45-50 grams per gram of activated carbon.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)
  • Carbon And Carbon Compounds (AREA)
  • Saccharide Compounds (AREA)

Abstract

A process for the purification of sugar liquors with activated carbon is described. The use of activated carbon with an iodine number at least 1000 and an average particle size in the range of 0.4 mm to 4.0 mm allows for increased flow rates resulting in high yield of purified sugar liquors.

Description

    BACKGROUND OF THE INVENTION
  • This invention is directed to a method of purification and decolorization of sugar liquors.
  • This invention especially relates to an improved method for the purification and decolorization of sugar liquors including starch hydrolyzates such as corn syrup.
  • More particularly, this invention provides for a purification of sugar liquors through the use of a special granular activated carbon resulting in final products of high purity.
  • The term, "sugar liquors," as used herein, includes solutions of starch hydrolyzate which contain a mixture of mono-, di-, and higher polysaccharides and it particularly includes sugar solutions derived from cane, beet and corn sources. The term, "oligosaccharide," as used herein, is a carbohydrate containing from 2 to 8 simple sugars linked together. Combinations of more than 8 simple sugars are polysaccharides. A starch hydrolyzate is defined as an aqueous mixture of sugar components derived from acid, enzyme or other treatment of starchy materials.
  • The purification of sugar liquors such as corn syrup, cane sugar and relatively impure solutions of dextrose is one of the oldest established industrial chemical procedures.
  • Aqueous solutions of certain sugars such as glucose occur industrially in the hydrolysis of amylaceous or cellulosic materials. For example, large quantities of glucose solutions are prepared by the hydrolysis of starch in the manufacture of corn syrup, corn sugar and dextrose. These solutions contain minor but significant amounts of other sugars not removed by conventional refining procedures.
  • One use for activated carbon is the decolorization of sugar liquors. Typically the powdered activated carbon is slurried with the impure liquor one or more times followed by filtration of the decolorized liquor. Decolorization is also accomplished by passing the liquors through a column of granular activated carbon. These procedures remove color-causing impurities but only incidental amounts of oligosaccharides present in the liquor.
  • Another use of activated carbon involves the adsorption of high molecular weight sugars in addition to color causing impurities. Activated carbon has been employed in a column chromatography system for removing such impurities from a glucose solution as described in U.S. Patent No. 2,549,840. Cakes of powdered activated carbon have been used in a series of filters to accomplish the removal of impurities from sugar liquors as described in U.S. Patent No. 3,551,203.
  • These purification techniques generally require either a large amount of activated carbon or suffer from low flow rates, resulting in a poor yield of purified sugar product.
  • SUMMARY OF THE INVENTION
  • The object of this invention is directed to an improved method for the purification of sugar liquors. Thus, there is shown the use of a special granular activated carbon which due to its high iodine number and large average particle size allows for a reduction in the amount of activated carbon necessary and for an increased flow rate through a carbon filter process such as described above. This invention allows the use of high flow rates with the benefit of increased yield of purified sugar product over the prior art. This high yield reduces both capital and operating cost for processes to remove oligosaccharides and polysaccharides from impure sugar liquors.
  • Thus there is provided an improvement in the method of purifying and decolorizing sugar liquors which includes contacting said sugar liquors with a sufficient amount of activated carbon to adsorb oligosaccharides containing 3 or more saccharide groups. Said contact is maintained for a period of time sufficient to accomplish substantially complete adsorption of said oligosaccharides. The improvement comprises the use of granular activated carbon with an iodine number of at least 1,000, preferably at least 1,200 and an'average particle size in the range of 0.4 mm to 4.0 0 mm.
  • DETAILED DESCRIPTION
  • The activated carbon employed in this improved method must have an iodine number of at least 1,000 and an average particle size in the range of 0.4 mm to 4.0 mm. Typical prior art activated carbons for use in sugar purification have had iodine numbers below 500. The iodine number is useful in quantifying the adsorbtive capacity of the activated carbon. The iodine number is defined as the milligrams of iodine adsorbed from an aqueous idodine-potassium iodine solution by one gram of activated carbon when the iodine concentration of the residual filtrate is 0.02 normal.
  • The method of application of the improved purification process of this invention can best be understood by reference to the purification of a corn syrup solution. A corn syrup solution by definition is a dextrose hydrolyzate of less than 99% dextrose. Dextrose, or D(+)-glucose has a variety of uses especially in its pure form. For example, dextrose with no impurities would give an excellent product to breweries for beer fermentation. The higher molecular weight sugars present in dextrose hydrolyzate, if not removed, would contribute to an increased caloric content of the final beer. High purity dextrose would also be an advantage in the production of sorbitol where the oligosaccharides of 3 or more sugars interfere with hydrogenation.
  • Although the present invention is described in connection with a preferred embodiment it is to be understood that modifications and variations may be used without departing from the spirit of the invention.
  • Enzymatic conversion of starch yields a dextrose hydrolyzate solution comprised of approximately 95-98% dextrose, 1-3% maltose (.DP-2) and approximately 1-2% maltotriose and higher saccharide sugars (DP-3 and DP-3+). The term "DP-n" refers to the degree of polymerization where n is the number of sugar units in the polymer. Thus, DP-n (where n=3 and above), represents the oligosaccharides to be adsorbed by the granular activated carbon as shown in this invention.
  • The dextrose hydrolyzate syrup to be purified can be treated as an aqueous solution of from 18.5 to 30.0% dry substance. The range is dependent on preventing decomposition of the liquor and on keeping the viscosity at a reasonable, i.e., workable level.
  • In general, the purification of the hydrolyzate solution is accomplished by passing the solution through a series of columns, containing granular activated carbon with an iodine number of at least 1,000 and with an average particle size in the range of 0.4 mm to 4.0 mm at a flow rate in a range of 1 to 3 gpm/ft. cross sectional area generating a contact time in each column in a range of about 10 to 30 minutes.
  • The following examples will more completely illustrate the practice of this invention. It will be readily understood that these examples should not be construed as limiting the scope of this invention in any way. They merely illustrate some of the many variations possible through the practice of this method.
  • EXAMPLE 1
  • A starch hydrolyzate, comprised of 97% dextrose, 2.4% DP-2, 0.2% DP-3 and 0.4% DP-4 was purified on a series of eight, four foot by one inch (i.d.) columns each loaded with 255 grams (600 cc) of granular activated carbon with an iodine number in the range of 1,000 to 1,050 and an average particle size in the range of 0.9 mm to 1.5 mm, at a flow rate of 20.8 ml/min. generating a contact time in each column of about 30 minutes. The yield of purified dextrose (98.5% dextrose - 1.5% DP-2) ) was between 20-25 grams per gram of activated carbon.
  • EXAMPLE 2
  • The starch hydrolyzate of Example 1 was purified through the series of columns of Example 1 loaded with granular activated carbon with an iodine number in the range of 1,200 to 1,400 and an average particle size in the range of 0.9 mm to 1.5 mm at a flow rate of 20.8 ml/min. generating a contact time in each column of about 30 minutes. The yield of purified dextrose was between 45-50 grams per gram of activated carbon.

Claims (2)

1. A method of purifying and decolorizing sugar liquors which includes contacting said sugar liquors with a sufficient amount of activated carbon to adsorb oligosaccharides containing 3 or more saccharide groups, maintaining said contact for a period of time sufficient to accomplish substantially complete adsorbtion of said oligosaccharides;
the method being characterized by :
using granular activated carbon with an iodine number of at least 1,000 and an average particle size in the range of 0.4 mm to 4.0 mm.
2..The method of Claim 1 wherein the granular activated carbon has an iodine number of at least 1,200.
EP82400341A 1981-03-02 1982-02-26 Purification of sugar liquors with activated carbon Withdrawn EP0059669A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US23983681A 1981-03-02 1981-03-02
US239836 1981-03-02

Publications (2)

Publication Number Publication Date
EP0059669A2 true EP0059669A2 (en) 1982-09-08
EP0059669A3 EP0059669A3 (en) 1984-08-15

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EP82400341A Withdrawn EP0059669A3 (en) 1981-03-02 1982-02-26 Purification of sugar liquors with activated carbon

Country Status (8)

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EP (1) EP0059669A3 (en)
JP (1) JPS5926280B2 (en)
AU (1) AU8062182A (en)
DK (1) DK88682A (en)
ES (1) ES8302782A1 (en)
GR (1) GR75513B (en)
NZ (1) NZ199763A (en)
PT (1) PT74479B (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2763580A (en) * 1951-01-29 1956-09-18 Pittsburgh Coke & Chemical Co Activated carbon treatment of sugar liquors and regeneration
US2969297A (en) * 1959-06-22 1961-01-24 American Sugar Refining Co Purification of beet sugar solutions
US2969298A (en) * 1959-06-22 1961-01-24 Spreckles Sugar Company Purification of beet sugar solutions

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2763580A (en) * 1951-01-29 1956-09-18 Pittsburgh Coke & Chemical Co Activated carbon treatment of sugar liquors and regeneration
US2969297A (en) * 1959-06-22 1961-01-24 American Sugar Refining Co Purification of beet sugar solutions
US2969298A (en) * 1959-06-22 1961-01-24 Spreckles Sugar Company Purification of beet sugar solutions

Also Published As

Publication number Publication date
JPS5926280B2 (en) 1984-06-26
DK88682A (en) 1982-09-03
ES510020A0 (en) 1983-01-16
GR75513B (en) 1984-07-25
NZ199763A (en) 1984-03-30
JPS57155999A (en) 1982-09-27
ES8302782A1 (en) 1983-01-16
PT74479B (en) 1984-10-09
PT74479A (en) 1982-03-01
EP0059669A3 (en) 1984-08-15
AU8062182A (en) 1982-09-09

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