CN1154960A - Method for recovering alanine from ion-exchanging eluent of gourmet production - Google Patents

Method for recovering alanine from ion-exchanging eluent of gourmet production Download PDF

Info

Publication number
CN1154960A
CN1154960A CN 96120065 CN96120065A CN1154960A CN 1154960 A CN1154960 A CN 1154960A CN 96120065 CN96120065 CN 96120065 CN 96120065 A CN96120065 A CN 96120065A CN 1154960 A CN1154960 A CN 1154960A
Authority
CN
China
Prior art keywords
resin
acid
elutriant
class
adsorption
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.)
Granted
Application number
CN 96120065
Other languages
Chinese (zh)
Other versions
CN1053181C (en
Inventor
宋正孝
马忠海
牛文泰
谌竞清
谢振风
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.)
Tianjin University
Original Assignee
Tianjin University
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 Tianjin University filed Critical Tianjin University
Priority to CN96120065A priority Critical patent/CN1053181C/en
Publication of CN1154960A publication Critical patent/CN1154960A/en
Application granted granted Critical
Publication of CN1053181C publication Critical patent/CN1053181C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)

Abstract

The present invention relates to a method for recovering alanine from ion exchange eluent in the production of monosodium glutamate, which is mainly characterized by making the eluent pass throughsuch processes of isolelectric crystallization, resin adsorption and separation, concentration, decolouring and crystallizationt reatment to obtain the alanine product whosse purity is up to above 98%. Said invention adopts the adsorbing columns which are respectively filled up with different resins to implement the adsorption and separation of impurities, salts and glutamic acid from eluent to obtain alanine. Said invention is simple in technological process, easy to operate and its recovering rate is high.

Description

From the ion-exchanging eluent of glutamate production, reclaim the method for L-Ala
The present invention relates to a kind of method that from the ion-exchanging eluent of glutamate production, reclaims L-Ala.It belongs to the technology of Separation and Recovery L-Ala in the glutamate production process.
L-Ala (being called for short Ala) is a kind of amino acid with higher economic worth.It is widely used in food, wine brewing, medicine, makeup, biochemical product, is preparation VB 6Basic raw material with mixed amino acid.
In the glutamic acid fermentation process of glutamate production, L-Ala is the intermediate product of biosynthesizing L-glutamic acid process, generally is about 1~2% of amount of glutamic acid.The patent of invention that each Gourmet Powder Factory of present China generally adopts this seminar to propose in 1988 " reclaims the novel process of L-glutamic acid " from the isoelectric point crystallization mother liquor (ZL88106847.0 authorizes day: 1992.4.15) flow process production monosodium glutamate.This extraction L-glutamic acid etc. electricity-as follows from the process flow of handing over:
Figure A9612006500031
As seen this technology is when reclaiming L-glutamic acid, and L-Ala has also obtained preliminary concentrating.Show that according to sample survey L-Ala content is 6~12g/L in elutriant, and recovery value is arranged very much to domestic each Gourmet Powder Factory.By domestic annual 300000 tons of monosodium glutamates, 3000~6000 tons of the recyclable L-Ala produced.This is an appreciable wealth.But glutamate production producer is but without any recovering means at present, and also not seeing in the document has the method report that reclaims L-Ala from ion-exchanging eluent.
The object of the present invention is to provide a kind of method that from the ion-exchanging eluent of glutamate production, reclaims L-Ala.This method has that operational path is simple, easy and simple to handle, less investment, characteristics that the rate of recovery is high.
In order to achieve the above object, the present invention has adopted following technical scheme to see in fact in addition.At first in ion-exchanging eluent (high flow liquid), add sulfuric acid (or hydrochloric acid) and carry out isoelectric point crystallization, and remove crystalline rough rice propylhomoserin, then isoelectric point crystallization mother liquor or elutriant (high flow liquid) are regulated PH successively, resin absorption is separated, is concentrated and the decolouring crystallization treatment, can obtain purity at last and reach L-Ala product more than 98%.The technical characterstic of this technological process is: add sulfuric acid or hydrochloric acid to isoelectric point crystallization mother liquor or elutriant and regulate PH and reach 1.5~2.0; Adsorption separation process is provided with the adsorption column of three classes filling different resins, filling ammonium type strong resin in the one class post, absorption paddy, L-Ala contain impurity, salt tail washings and discharge, saturated resin feeds the two class posts or the three class posts in step down with ammonium hydroxide wash-out regeneration, elutriant; Two class posts filling carboxylic acid type weak acid resin mainly adsorbs ammonium ion and other cation impurity, and saturated resin is regenerated with the sulfuric acid of 0.5~1M or the hydrochloric acid wash-out of 1~1.5M, and elutriant contains ammonium sulfate or ammonium chloride is discharged, and the adsorption column effluent liquid enters three class posts; Filling primary amine type weak base resin mainly adsorbs L-glutamic acid in the three class posts, and the post effluent liquid feeds the absorption evaporating column, and saturated resin is regenerated with the ammonium hydroxide of 1~2M or the sodium hydroxide wash-out of 1~2M, and elutriant removes to reclaim L-glutamic acid or refining gourmet powder; Filling hydrogen type strong acid resin mainly adsorbs L-Ala in the absorption evaporating column in the concentration process, the effluent liquid discharging, and saturated resin is regenerated with the ammonium hydroxide wash-out, and elutriant removes vacuum concentration.
Accompanying drawing is a process flow sheet of the present invention.
Below in conjunction with the technological process accompanying drawing the present invention is elaborated. Eluent (the height that is got off by former technology intermediate ion exchange column Flow liquid) in, contain glutamic acid, alanine and inorganic salts and impurity, in order effectively alanine to be separated recovery from this solution, At first salt and impurity be need remove, and then glutamic acid, alanine and ammonium separated. The present invention is at first to the ion-exchange wash-out for this reason Add sulfuric acid (or hydrochloric acid) in the liquid (high flow liquid) and carry out isoelectric point crystallization, and except the rough rice propylhomoserin that decrystallizes, afterwards to crystalline mother solution Regulate PH to 1.5~2.0, in order to carry out adsorbing separation: filling ammonium type strong resin in the class adsorption column, this resin pair Glutamic acid, alanine have good adsorptivity, so adsorption liquid can be removed wherein inorganic salts and assorted by this adsorption column After matter, saturated resin were regenerated with the ammonium hydroxide wash-out, its eluent mainly contained alanine, glutamic acid and ammonium, and this eluent enters Two class adsorption columns or three class adsorption columns. Filling carboxylic acid type weak acid resin in the two class posts, this post further adsorbs ammonium ion, isolates Ammonium, this post efflux enter three resinoid posts of filling primary amine type resin, and this resin mainly adsorbs glutamic acid, and main in the efflux Contain alanine and enter concentrated adsorption column. This post adsorbs saturated rear resin with ammonium hydroxide or NaOH wash-out, and its eluent goes Reclaim glutamic acid or refining gourmet powder. Concentrate dress hydrogen type strong acid resin in the adsorption column, this post mainly adsorbs alanine, adsorb saturated after Carry out wash-out regeneration with ammonium hydroxide, eluent is the higher alanine solution of concentration, and then concentrates and use and live through reduction vaporization The property carbon decoloring adds industrial alcohol again and can prepare purity and reach industrial alanine product more than 98%.
The process route of recovery alanine of the present invention is simple, and is easy to operate, less investment, rate of recovery height. The enforcement of this method, no But can reclaim the alanine of higher economic worth, increase economic efficiency, and can reduce again alanine and wait electricity-ion-exchange Accumulation cycle in the method glutamate production process, thus the glutamate production operating cost reduced, also reduced production process simultaneously to ring The pollution in border.
Embodiment:
With 2.8 liters of content is [Glu]=65g/l, [Ala]=8g/l, [NH 4 +]=10.6g/l from handing over elutriant, behind the sulfuric acid isoelectric point crystallization, can obtain 2.5 liters from handing over electric mother liquor such as wash-out, contain [Glu]=15g/l, [Ala]=8g/l, [(NH 4) 2SO 4]=39.6g/l.These electric mother liquors are gone up ammonium type strong resin post absorption L-glutamic acid, L-Ala after transferring PH with acid, to remove ammonium sulfate.This saturated column can obtain about 1 liter of content behind the ammonium hydroxide wash-out be [Glu]=34.5g/l, [Ala]=18.1g/l, [NH 4 +The desalination elutriant of]=9g/l, this solution stream further removes L-glutamic acid and residual other positively charged ion, negatively charged ion through carboxylic acid type weak acid resin-primary amine type weak base resin post.To not be adsorbed and flow into the hydrogen type strong acid resin column and concentrate and between PH4~8, be in electroneutral L-Ala.The clearance of this operation L-glutamic acid is near 100% after measured, and the yield of L-Ala is 81.6%.After the L-Ala that flows into the hydrogen type strong acid resin column is adsorbed enrichment,, obtain the L-Ala solution of the about 80~100g/l of concentration with the ammonium hydroxide wash-out that makes the transition.Slough the ammonia of moisture content and trace again through vacuum concentration, when concentration reaches 240g/l,, add an amount of industrial spirit and promptly obtain L-Ala crystalline product 13.4g by behind the activated carbon decolorizing.Greater than 98%, meet industrial L-Ala standard through chemical examination purity.Be about 67% by the L-Ala total recovery that enters the calculating of L-Ala abstraction process from electric mother liquors such as handing over wash-out.Can obtain simultaneously with sodium hydroxide by the about 2.4kg of Sodium Glutamate under the primary amine type weak base resin post wash-out.

Claims (1)

1. reclaim the method for L-glutamic acid the ion-exchanging eluent from glutamate production (high flow liquid), it is to add acid to elutriant (high flow liquid) to carry out isoelectric point crystallization, remove the rough rice propylhomoserin that decrystallizes, then to isoelectric point crystallization mother liquor or elutriant (high flow liquid) regulate PH, ion exchange resin fractionation by adsorption successively, concentrate, the decolouring crystallization treatment, obtain purity and reach L-Ala product more than 98%.The technical characterictic of this technological process is:
A. add sulfuric acid or hydrochloric acid adjusting PH to isoelectric point crystallization mother liquor or elutriant, reach 1.5~2.0;
B. filling ammonium type strong resin in the class post of fractionation by adsorption adsorbs paddy, L-Ala, contains impurity, salt tail washings and discharge, saturated resin ammonium hydroxide wash-out regeneration, the two class posts or the three class posts in step under elutriant feeds;
C. load the carboxylic acid type weak acid resin in the two class posts of fractionation by adsorption, main absorption ammonium ion and other cation impurity, saturated resin is regenerated with the sulfuric acid of 0.5~1M or the hydrochloric acid wash-out of 1~1.5M, and elutriant contains ammonium sulfate or ammonium chloride is discharged, and the adsorption column effluent liquid feeds three class posts;
D. filling primary amine type weak base resin in the three class posts of fractionation by adsorption mainly adsorbs L-glutamic acid, and effluent liquid feeds the absorption evaporating column, and saturated resin is regenerated with the ammonium hydroxide of 1~2M or the sodium hydroxide wash-out of 1~2M, and elutriant removes to reclaim L-glutamic acid or refining gourmet powder;
E. filling hydrogen type strong acid resin in the absorption evaporating column in the concentration process mainly adsorbs L-Ala, the effluent liquid discharging, and saturated resin is regenerated with the ammonium hydroxide wash-out, and elutriant removes vacuum concentration.
CN96120065A 1996-10-18 1996-10-18 Method for recovering alanine from ion-exchanging eluent of gourmet production Expired - Fee Related CN1053181C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN96120065A CN1053181C (en) 1996-10-18 1996-10-18 Method for recovering alanine from ion-exchanging eluent of gourmet production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN96120065A CN1053181C (en) 1996-10-18 1996-10-18 Method for recovering alanine from ion-exchanging eluent of gourmet production

Publications (2)

Publication Number Publication Date
CN1154960A true CN1154960A (en) 1997-07-23
CN1053181C CN1053181C (en) 2000-06-07

Family

ID=5126111

Family Applications (1)

Application Number Title Priority Date Filing Date
CN96120065A Expired - Fee Related CN1053181C (en) 1996-10-18 1996-10-18 Method for recovering alanine from ion-exchanging eluent of gourmet production

Country Status (1)

Country Link
CN (1) CN1053181C (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113716749A (en) * 2021-09-09 2021-11-30 胡建康 Method for removing COD (chemical oxygen demand) in high-salinity wastewater
CN114276262A (en) * 2021-10-22 2022-04-05 欧尚元(天津)有限公司 Method for separating alanine
CN115583892A (en) * 2022-11-08 2023-01-10 秦皇岛华恒生物工程有限公司 Preparation method of high-quality beta-alanine and impurity removal method

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6244191A (en) * 1985-08-23 1987-02-26 Toray Ind Inc Production of l-threonine by fermentation
JPH01102051A (en) * 1987-10-15 1989-04-19 Mitsui Toatsu Chem Inc Production of alanine
CN1015173B (en) * 1988-09-26 1991-12-25 天津大学 Process for the recovery of glutamic acid from isoelectric point crystallizing mother liquor
CN1094708A (en) * 1993-05-06 1994-11-09 冯容保 Process for recovering glutamic acid by full mother liquor ion exchange method

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113716749A (en) * 2021-09-09 2021-11-30 胡建康 Method for removing COD (chemical oxygen demand) in high-salinity wastewater
CN114276262A (en) * 2021-10-22 2022-04-05 欧尚元(天津)有限公司 Method for separating alanine
CN115583892A (en) * 2022-11-08 2023-01-10 秦皇岛华恒生物工程有限公司 Preparation method of high-quality beta-alanine and impurity removal method
CN115583892B (en) * 2022-11-08 2024-03-29 秦皇岛华恒生物工程有限公司 Preparation method of high-quality beta-alanine and impurity removal method

Also Published As

Publication number Publication date
CN1053181C (en) 2000-06-07

Similar Documents

Publication Publication Date Title
CN102534214B (en) Method for recycling gallium from Bayer mother solution by using chelate resin
CN102432479B (en) Method for extracting L-valine from L-valine fermentation liquid
CN101168512A (en) Method for separating and purifying valine from valine liquid
CN105646256A (en) Glutamic acid extraction crystallization process
CN105420495B (en) In a kind of Bayer process alumina producing in gallium processing procedure uranium separation method
CN1035000C (en) Method of extracting citric acid from citric acid fermentation liquor
CN107519948A (en) Composite amino weakly-alkaline anion exchange resin and method for recovering rhenium from arsenic sulfide slag leachate
CN101367743A (en) Method for separation purification of isoleucine from isoleucine liquid
CN1053181C (en) Method for recovering alanine from ion-exchanging eluent of gourmet production
CN106834687A (en) A kind of method for extraction and purification of lanthana
CN109628767B (en) Method for preparing ultra-pure rare earth oxide by normal-temperature high-pressure ion exchange
CN103918873A (en) Comprehensive utilization process of glutamic acid crystal mother liquid
CN111560529A (en) Method for recovering germanium from germanium-containing material
CN101186582B (en) Method for separating and purifying phenylalanine from phenylalanine fermentation liquor
CN100339357C (en) Hind extraction process for producing L-phenylalanine using phenyl-pyruvic acid enzyme method
CN1332034C (en) Process for producing citric acid and/or citrate
CN1031527A (en) From isoelectric point crystallizing mother liquor, reclaim the novel process of L-glutamic acid
CN113735136B (en) Process method for preparing potassium salt and byproduct magnesium salt by using corn soaking water
CN1056190C (en) Citric acid extracting process
CN1067677C (en) L-glutamine separating and purifying process
CN1056191C (en) Trisodium citrate preparing process using anion exchange resin
CN1113054C (en) Process for preparation of monosodium glutamate
CN1186312C (en) Method for separating and purifying ephedrine by using weak acid cation exchange resin and macroporous resin
CN113387987A (en) Recovery application of 5 '-AMP and 5' -UMP in nucleotide chromatographic separation
CN106756019A (en) A kind of method for extraction and purification of gadolinium oxide

Legal Events

Date Code Title Description
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C06 Publication
PB01 Publication
C14 Grant of patent or utility model
GR01 Patent grant
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee