US2842591A - Process of treating sugar beet molasses to recover barium saccharate and glutamic acid - Google Patents

Process of treating sugar beet molasses to recover barium saccharate and glutamic acid Download PDF

Info

Publication number
US2842591A
US2842591A US547039A US54703955A US2842591A US 2842591 A US2842591 A US 2842591A US 547039 A US547039 A US 547039A US 54703955 A US54703955 A US 54703955A US 2842591 A US2842591 A US 2842591A
Authority
US
United States
Prior art keywords
barium
glutamic acid
molasses
sugar
saccharate
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.)
Expired - Lifetime
Application number
US547039A
Other languages
English (en)
Inventor
James L Shelton
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.)
International Minerals and Chemical Corp
Original Assignee
International Minerals and Chemical 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
Priority to NL96340D priority Critical patent/NL96340C/xx
Priority to NL211346D priority patent/NL211346A/xx
Application filed by International Minerals and Chemical Corp filed Critical International Minerals and Chemical Corp
Priority to US547039A priority patent/US2842591A/en
Application granted granted Critical
Publication of US2842591A publication Critical patent/US2842591A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C13SUGAR INDUSTRY
    • C13BPRODUCTION OF SUCROSE; APPARATUS SPECIALLY ADAPTED THEREFOR
    • C13B35/00Extraction of sucrose from molasses
    • C13B35/02Extraction of sucrose from molasses by chemical means
    • C13B35/04Extraction of sucrose from molasses by chemical means by precipitation as alkaline earth metal saccharates

Definitions

  • This invention relates to the processing of sugar beet molasses, and more particularly, to the removal of sugar values from sugar beet molasses in such a manner that the nitrogenous volues contained in the molasses are preserved.
  • Precipitation of sugar values in sugar beet molasses as barium saccharate, acidulation of the barium saccharate to free the sugar and recover the same by crystallization is a well known commercial process.
  • the conditions of precipitation, the weight ratio of barium oxide to sugar contained in the molasses, the temperature of the molasses during precipitation and the processing of the waste Water are usually all adjusted and designed to recover the highest possible economic yield of crystal sugar per unit weight of molasses treated.
  • Nitrogenous values originally contained in the beet molasses are recovered by subsequently hydrolyzing the barium process filtrate to convert the glutamine and/ or pyrrolidone-carboxylic acid content to glutamic acid. Hydrolysis is accomplished either through the use of strong alkalis, such as caustic soda, or strong acids, such as hydrochloric acid. Glutamic acid may be crystallized from the hydrolyzate at its isoelectric point.
  • Another object of this invention is to provide a process for recovering sugar from sugar beet molasses while simultaneously substantially completely converting glutamic acid precursors to glutamic acid in a manner to avoid destruction of glutamic acid values and to afford emcient recovery of barium for reuse.
  • sugar beet molasses is treated with a barium oxide compound, that is, barium oxide or barium hydroxide, in an aqueous medium at a temperature of at least 50 C. until reaction between the barium and sugar and hydrolysis of glutamic acid precursor compounds are substantially complete.
  • barium oxide or the barium oxide equivalent of barium hydroxide must be present in. an amount of at least 60% of-the weight of the sugar in the molasses.
  • Glutamic acid may be recovered from the hydrolyzate by conventional means following separation of the barium saccharate formed.
  • Barium saccharate may be recovered from the reaction mixture by any convenient means as by filtration, and treated according to conventional procedures to recover the sugar and the barium.
  • the barium saccharate cake is slurried in water and the slurry carbonated'by passing carbon dioxide through the slurry nited States Patent "ice until substantially all barium is in the form of barium carbonate.
  • the latter is insoluble and may be filtered from the reaction mixture.
  • Mother liquor remaining which contains dissolved sugar may be treated to crystallize the sugar therefrom.
  • Barium carbonate thus recovered may be calcined to produce barium oxide and the latter used for treating a fresh quantity of molasses.
  • Sugar beet molasses ordinarily has a solids content of the order of between about 83% and about 87% by weight.
  • the molasses be diluted with water or an aqueous solution containing barium oxide to produce a more workable consistency and to insure intimate contact with the barium oxide compound to be added.
  • the molasses therefore, is admixed with sufiicient water to reduce its solids content to less than about 70% by Weight.
  • sufiicient water to reduce its solids content to less than about 70% by Weight.
  • Barium oxide or barium hydroxide is utilized in this invention in an amount equivalent to at least about 60% by weight barium oxide based on the weight of sugar in the molasses.
  • the barium oxide compound is present in an amount equivalent to between about 65% and about 85% barium oxide based on the weight of sugar in molasses, this quantity of barium oxide compound permitting completion of the reaction in shorter periods of time and at lower temperatures. More than 85% barium oxide may be used, but there is little, if any,
  • Addition of the barium oxide compound to the dilute molasses is desirably effected by slurrying the barium oxide compound in sufficient water to facilitate handling and to insure intimate contact of the barium oxide compound with the sugar in the molasses. While solid barium oxide or barium hydroxide may be utilized, there is difficulty in obtaining intimate contact between the solid barium oxide compound and the molasses under these conditions and this method is less desirable.
  • the barium oxide compound will be admixed with between about two and about four times its weight of water and the resulting slurry added to the dilute molasses. Excessive Water is undesirable because the excess will ultimately have to be removed, thereby adding to' the cost of the overall process. For convenience and ease of handling it is desirable to maintain the barium oxide slurry at a temperature of at least 65 C.
  • barium oxide compound refers to barium oxide or barium hydroxide. All reference to quantities or percentages of barium oxide compound refer to barium oxide itself or the barium oxide equivalent of barium hydroxide.
  • the process of this invention is carried out at a temperature above about 50 C., and preferably, at a temperature between about 60 C. and about 85 C. Temperatures below about 50 C. are avoided as resulting in such slow hydrolysis rates of glutamic acid precursor compounds as to be impractical. Best reaction rates are Obtained at temperatures between about 60 C. and about 85 C.
  • substantially complete hydrolysis of the glutamic acid precursor compounds and substantially complete precipitation of the sugar content of the molasses may be obtained in a relatively short period of time, this is, within a few hours, if the quantity of reagents and other reaction conditions are properly correlated.
  • Barium saccharate produced by reaction of the barium oxide compound and sugar present in the molasses is removed from the reaction product mixture by any convenient means, for example by filtration.
  • Barium saccharate cake is preferably washed with a dilute barium oxide or barium hydroxide solution to remove any residual liquor from the cake.
  • the wash solution preferably contains between about 1% and about 3% barium oxide, by weight, and more preferably about 2% barium oxide, by weight. Wash solution recovered from the washing of the barium saccharate cake is, in accordance with a preferred embodiment of this invention, used to dilute fresh molasses and replaces fresh water for this purpose.
  • Dilution of fresh molasses with this wash solution also permits a savings in barium oxide and increases recoveries of glutamic acid values under certain conditions. For example, with a one-half hour reaction time at 80 C. and utilizing 60% barium oxide based on the weight of sugar, highest recoveries of glutamic acid values are obtained by recycling 83% of the barium saccharate wash solution, and at 50 C. under the same conditions, best recoveries are obtained using 100% recycle of wash solution.
  • barium saccharate wash solution may b mixed with any amount of fresh water prior to dilution of molasses but preferably about 83% of the wash solution will be recycled and utilized for diluting fresh molasses.
  • the most complete hydrolysis of glutamic acid values is obtained by reacting a molasses diluted being fresh water), and reacted with about 80% barium oxide based on the sugar for about two hours at about 80 C.
  • a dilute molasses is reacted with about 70% barium oxide based on the sugar in the molasses at about 65 C.
  • the mother liquor remaining following the removal of the barium saccharate precipitate is termed barium filtrate and contains substantially all of the glutamic acid values.
  • Recovery of the glutamic acid from the barium filtrate in accordance with this invention involves first removing barium ions from the solution by treatment with sodium carbonate, or potassium carbonate, or by passing a carbon dioxide-containing gas through the filtrate until the pH is adjusted to between about 8 and about 10, preferably between about 8.5 and about 9.5.
  • the glutamic acid In order to recover the glutamic acid from the solution, it is concentrated to at least about solids and preferably to about solids. Following concentration, the filtrate is next treated in a manner depending upon whether glutamic acid is to be recovered immediately or whether the concentrated filtrate is to be stored prior to recovery. Storing the concentrated filtrate without further treatment results in the destruction of substantial quantities of glutamic acid present. However, concentrated filtrate may be stored for long periods of time without loss of glutamic acid if the pH of the concentrated filtrate is first adjusted to between about pH 6 and about pH 8, preferably to about pH 7. Adjustment of the pH may be made by the addition of a suitable inorganic acid, such as hydrochloric acid.
  • a suitable inorganic acid such as hydrochloric acid.
  • an inorganic acid such as hydrochloric acid
  • hydrochloric acid is added to adjust the pH to between about 5 and about 6, preferably to about pH 5.4.
  • the adjusted filtrate is then further concentrated with the result that inorganic salts precipitate.
  • the mother liquor is adjusted to about pH 3.2 by the further addition of hydrochloric acid, and glutamic acid is crystallized from the adjusted solution in accordance with conventional procedures.
  • Example I Beet molasses having a solids content of about 85% and containing about 100 parts of sugar was diluted with fresh water in an amount equal to of the weight of the molasses and the mixture heated to C. To the heated mixture was added 80 parts of barium oxide in the form of a suspension in 236 parts of water at 80 C. The admixture was maintained at 80 C. for about two hours and then filtered to remove the barium saccharate which had formed. In order to remove entrained liquor from the barium saccharate cake, the latter was washed with about 300 pounds of an aqueous barium oxide solution containing about 2% barium oxide at a temperature of 80 C.
  • Glutamic acid was recovered from both of the above filtrates in accordance with the conventional procedures by adjusting the pH of the filtrates to about 3.2 with hydrochloric acid and crystallizing glutamic acid from the solution.
  • Example 11 Beet molasses having a solids content of about 85 and containing 100 parts of sugar was diluted with about 150 parts of wash solution from a previous barium saccharate filtration. About 150 parts of wash solution containing about 2% barium oxide by weight was utilized. After heating the diluted molasses to 80% C. a slurry of barium oxide in 150 parts of additional wash solution from the previous filtration was added, the slurry containing 73 parts of fresh barium oxide and 5.8 parts of barium oxide already in the wash liquors. The total barium oxide added amounted to 80% of the sugar in the molasses plus recycled wash solution. After holding the mixture at 80% C.
  • barium saccharate cake washed with 300 parts of a barium oxide solution at 80 C., the solution containing about 2% barium oxide by weight. Barium saccharate cake was obtained in an amount indicating that the precipitation of sugar was about 97% complete. Glutamic acid precursor compounds in the molasses were found to have been 98% hydrolyzed.
  • Glutamic acid was recovered from the barium saccharate filtrate by passing carbon dioxide gas through the filtrate until the pH was adjusted to about 8.6, separating the barium carbonate precipitate by filtration, concentrating the filtrate to 60% solids, adjusting the pH of the concentrated liquor to about 5.4 by the addition of hydrochloric acid, concentrating again and separating inorganic salts from the concentrated liquor, adjusting the remaining liquor to pH 3.2 by the further addition of hydrochloric acid, and crystallizing glutamic acid from the adjusted liquor.
  • Example III Beet molasses containing about 100 parts of sugar was diluted with fresh water in an amount of about 75% of the weight of molasses and heated to 80 C. A 50% sodium hydroxide solution in the amount of 11 parts was added to the diluted molasses and then 70 parts of barium oxideslurried in 225 parts of water was added, the slurry having a temperature of 80 C. The admixture was maintained at 80 C. for two hours and then filtered to remove the barium saccharate solids. Following washing of the filter cake with 300 parts of a 2% barium oxide solution at 80 0., there was obtained 170 pounds of dry barium saccharate showing that sugar precipitation was 96.3% complete.
  • a process which comprises treating sugar beet molasses with at least about 60% by weight of barium oxide, based on the weight of sugar in the molasses, at a temperature between about 60 and about 85 C. for a period of about one-half to about five hours, varying inversely with the temperature, in an aqueous medium having a dry substance content between about 40 and about by weight, exclusive of the barium oxide and containing recycled barium saccharate cake wash liquor obtained in a subsequent step of the process, whereby the sugar is precipitated as barium saccharate and the glutarnic acid precursor compounds in said molasses are substantially completely hydrolyzed to glutamic acid, separating the barium saccharate precipitate from the reaction product mixture, washing said precipitate with a dilute aqueous barium oxide solution, recycling between about and about 100% of the resulting wash liquor to the treatment of additional molasses, and recovering glutamic acid from the barium saccharate mother liquor.
  • a process which comprises treating sugar beet molasses with at least about 60% by weight of barium oxide, based on the weight of sugar in the molasses, at a temperature between about 60 and about C. for a period of about one-half to about five hours, varying inversely with the temperature, in an aqueous medium having a dry substance content between about 40 and about 70% by weight, exclusive of the barium oxide, and containing recycled barium saccharate cake wash liquor obtained in a subsequent step of the process, whereby the sugar is precipitated as barium saccharate and the glutamic acid precursor compounds in said molasses are substantially completely hydrolyzed to glutamic acid, separating the barium saccharate precipitate from the reaction product mixture, washing said precipitate with a dilute aqueous barium oxide solution, recycling between about 80 and about of the resulting wash liquor to the treatment of additional molasses, adding between about 0.4 and about 3% of an alkali-metal hydroxide to the barium saccharate mother liquor, passing a carbon
  • a process which comprises treating sugar beet molasses with at least about 60% by weight of barium oxide, based on the weight of sugar in the molasses, at a temperature between about 60 and about 85 C. for a period of about one-half to about five hours, varying inversely with the temperature, in an aqueous medium having a dry substance content between about 40 and about 70% by weight, exclusive of the barium oxide,

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Organic Chemistry (AREA)
  • Fertilizers (AREA)
US547039A 1955-11-15 1955-11-15 Process of treating sugar beet molasses to recover barium saccharate and glutamic acid Expired - Lifetime US2842591A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
NL96340D NL96340C (fr) 1955-11-15
NL211346D NL211346A (fr) 1955-11-15
US547039A US2842591A (en) 1955-11-15 1955-11-15 Process of treating sugar beet molasses to recover barium saccharate and glutamic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US547039A US2842591A (en) 1955-11-15 1955-11-15 Process of treating sugar beet molasses to recover barium saccharate and glutamic acid

Publications (1)

Publication Number Publication Date
US2842591A true US2842591A (en) 1958-07-08

Family

ID=24183094

Family Applications (1)

Application Number Title Priority Date Filing Date
US547039A Expired - Lifetime US2842591A (en) 1955-11-15 1955-11-15 Process of treating sugar beet molasses to recover barium saccharate and glutamic acid

Country Status (2)

Country Link
US (1) US2842591A (fr)
NL (2) NL96340C (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012031270A1 (fr) * 2010-09-02 2012-03-08 Hcl Cleantech Ltd Procédés et systèmes de traitement de mélanges de sucre et compositions ainsi obtenues

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1686440A (en) * 1926-09-23 1928-10-02 Henry W Dahlberg Recovering sucrose from mixtures containing reducing sugars
US2373342A (en) * 1943-09-06 1945-04-10 Int Minerals & Chem Corp Manufacture of glutamic acid
US2535117A (en) * 1948-06-15 1950-12-26 Great Western Sugar Co Process for recovery of glutamic acid and other values from steffen waste water

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1686440A (en) * 1926-09-23 1928-10-02 Henry W Dahlberg Recovering sucrose from mixtures containing reducing sugars
US2373342A (en) * 1943-09-06 1945-04-10 Int Minerals & Chem Corp Manufacture of glutamic acid
US2535117A (en) * 1948-06-15 1950-12-26 Great Western Sugar Co Process for recovery of glutamic acid and other values from steffen waste water

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012031270A1 (fr) * 2010-09-02 2012-03-08 Hcl Cleantech Ltd Procédés et systèmes de traitement de mélanges de sucre et compositions ainsi obtenues
US9663836B2 (en) 2010-09-02 2017-05-30 Virdia, Inc. Methods and systems for processing sugar mixtures and resultant compositions
US10240217B2 (en) 2010-09-02 2019-03-26 Virdia, Inc. Methods and systems for processing sugar mixtures and resultant compositions

Also Published As

Publication number Publication date
NL96340C (fr)
NL211346A (fr)

Similar Documents

Publication Publication Date Title
US3998878A (en) Selectively separating oxalic, tartaric, glyoxylic and erythronic acids from aqueous solutions containing the same
US3666647A (en) Separation of fructose and glucose
US3429777A (en) High purity magnesium lactate from steepwater
US3872166A (en) Improvement in the recovery of glyoxylic acid
US2535117A (en) Process for recovery of glutamic acid and other values from steffen waste water
US2849468A (en) Amino acid derivatives
US2842591A (en) Process of treating sugar beet molasses to recover barium saccharate and glutamic acid
US2583591A (en) Method for recovery of vanadium-free chromate
US2456470A (en) Refining of inositol solutins
US2072919A (en) Process for producing citric acid
US2929839A (en) Process for recovering glutamic acid
US1754207A (en) Treatment of residual liquors
US2303602A (en) Calcium tartrate production
US2688037A (en) Manufacture of glutamic acid
US2796434A (en) Recovery of glutamic acid values
US2419020A (en) Calcium tartrate recovery process
US2730545A (en) Recovery of glutamic acid
US2706737A (en) Recovery of glutamic acid
US2842592A (en) Glutamic acid recovery
US2330785A (en) Method of making dextrose
US2829161A (en) Production of monosodium glutamate
US3172830A (en) Koh ore
US1634222A (en) Process of preparing betaine hydrochloride
US2796433A (en) Process for producing glutamic acid
US2799704A (en) Auto hydrolysis of barium filtrate