CN102061105A - Method for digesting plant water-soluble pigment from mobile solid phase material in continuous gradient manner - Google Patents

Method for digesting plant water-soluble pigment from mobile solid phase material in continuous gradient manner Download PDF

Info

Publication number
CN102061105A
CN102061105A CN2010105828068A CN201010582806A CN102061105A CN 102061105 A CN102061105 A CN 102061105A CN 2010105828068 A CN2010105828068 A CN 2010105828068A CN 201010582806 A CN201010582806 A CN 201010582806A CN 102061105 A CN102061105 A CN 102061105A
Authority
CN
China
Prior art keywords
lixiviate
jar
phase material
solid
mesh bag
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.)
Pending
Application number
CN2010105828068A
Other languages
Chinese (zh)
Inventor
梅元碧
倪建辉
程含友
梅宏
张�浩
王�琦
汪修武
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.)
WUHAN GREEN FOOD BIOLOGICAL ENGINEERING Co Ltd
Original Assignee
WUHAN GREEN FOOD BIOLOGICAL ENGINEERING Co Ltd
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 WUHAN GREEN FOOD BIOLOGICAL ENGINEERING Co Ltd filed Critical WUHAN GREEN FOOD BIOLOGICAL ENGINEERING Co Ltd
Priority to CN2010105828068A priority Critical patent/CN102061105A/en
Publication of CN102061105A publication Critical patent/CN102061105A/en
Pending legal-status Critical Current

Links

Images

Landscapes

  • Extraction Or Liquid Replacement (AREA)

Abstract

The invention discloses a method for digesting a plant water-soluble pigment from a mobile solid phase material in a continuous gradient manner, which comprises the steps of: covering the solid phase material with a net bag and transferring the solid phase material from one leaching tank to the other leaching tank by adopting a lifting device, keeping a leach liquor immovable during the transferring until the leach liquor in the leaching tank where the solid phase material is firstly dipped reaches the preset color value required by the process, and transferring the liquid material to a filter for carrying out subsequent working sequences. Because a mode that the solid phase material is only moved and the leaching solution is kept immovable within a working period is adopted, a plurality of leaching tanks naturally form a concentration gradient and are sequentially leached from a large gradient to a small gradient so as to be convenient for continuous production, improve the production capacity and be easy to obtain the leaching solution with higher concentration, thus the subsequent treatment is greatly reduced, the energy consumption is reduced, the yield is improved; the invention has the advantages of less equipment investment and simplicity of operation; and solid and liquid are discharged cleanly and conveniently, thus the blockage of the solid material is completely avoided.

Description

A kind of method of mobile solid-phase material continuous gradient lixiviate plant water-soluble pigment
The ㈠ technical field: the present invention relates to a kind of method of extracting the plant water-soluble pigment, specifically is a kind of method of mobile solid-phase material continuous gradient lixiviate plant water-soluble pigment.
㈡ background technology: at present, extract the plant water-soluble pigment, sweet potato is red as extracting from sweet potato, cabbage red, sailor yellow, extracts the method for Gardenia Yellow from cape jasmine, mainly adopts single-stage circulation dipping extract technology, promptly earlier meal is thinly sliced or broken into to sweet potato or cape jasmine and place the lixiviate jar, with water or sour water, buck is solvent, under the condition of normal temperature or heating, extracts with the pump circulation, behind the circulation maceration certain hour leach liquor emitted and goes to next procedure and handle, after concentrating and separating promptly.Solid-phase material is then discharged from the lixiviate pot bottom; Because whole technology is batch operation, and solid-phase material very easily cause jar at the bottom of screen cloth and line clogging short circuit, cause feed liquid to circulate, can't produce and put dried drop to the greatest extent, make extraction insufficient not exclusively, throughput is low, extraction efficiency is low, so the raw material extraction yield generally can only reach 80%-90%.
The ㈢ summary of the invention: purpose of the present invention just provides a kind of raw material extraction yield height, and solid-liquid changes
Move smooth and easy, production efficiency height, the method for a kind of mobile solid-phase material continuous gradient lixiviate plant water-soluble pigment that equipment requirements is low.
Technology of the present invention is made up of following step:
Figure 2010105828068100002DEST_PATH_IMAGE001
, according to the characteristic of solid-phase material, with itself break into meal or cut into slices, bar, place the mesh bag A that adapts with the solid-phase material globule size;
B, at No. 1, No. 2 ... add the extraction solvent of phase isodose in the N lixiviate jar successively respectively, the ratio of extraction solvent and solid-phase material is 3-10:1(V/W); And, adjust suitable pH value according to concrete material properties, and the control solvent temperature is 25-55 ℃, every jar of extraction time is 30-60 minute;
C, mesh bag A is put into the lixiviate jar No. 1 by lifting gear, after lixiviate finishes, it is mentioned from the lixiviate jar, above the jar mouth, stopped drop 3-5 minute; It is moved to successively next No. 2, No. 3, No. 4 again ... in the N lixiviate jar;
D, when mesh bag A moves to No. 2 lixiviate jars lixiviate from No. 1 lixiviate jar, inserted the solid-phase material of isodose mutually among the mesh bag B with mesh bag A, mesh bag B is inserted in No. 1 lixiviate jar after the lixiviate, take the move mode identical again, move to No. 2, No. 3 of back respectively with mesh bag A ... in the N lixiviate jar; And the like, mesh bag C, mesh bag D ... mesh bag N puts into the lixiviate jar successively No. 1, and moves backward in regular turn by above-mentioned same operation, vat liquor look valency in No. 1 lixiviate jar reaches the preset value of processing requirement, emit the vat liquor in the lixiviate jar No. 1, filter, filtrate is delivered to the concentrating and separating operation; So far finish a work period;
E, second work period begin, the extraction solvent that in No. 1 lixiviate jar of vacating, adds the phase isodose earlier, in this work period, each solid-phase material is all since the lixiviate of No. 2 lixiviate jars, and then move to successively No. 3, No. 4 ... N number, in No. 1 lixiviate jar, i.e. the lixiviate of solid-phase material is according to the concentration gradient lixiviate from large to small of vat liquor; After the vat liquor look valency in No. 2 lixiviate jars reaches the processing requirement preset value, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes second work period;
F, the 3rd work period begin, solid-phase material is since the lixiviate of No. 3 lixiviate jars, and then move to successively No. 4, No. 5 ... N number, No. 1, in No. 2 lixiviate jars, after the vat liquor look valency in No. 3 lixiviate jars reaches the processing requirement preset value, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes the 3rd work period; Used extraction solvent, extraction time and temperature of above-mentioned each work period be identical with described in the step b all; So circulation continuous gradient lixiviate, in each work period, remain solid-phase material vat liquor concentration maximum in that lixiviate jar of submerged first, and that lixiviate jar that newly adds extraction solvent immerses solid-phase material at last, vat liquor concentration is also minimum, circulation cover bubble will meet the requirements of vat liquor and emit successively, and the solid-phase material that lixiviate is finished discards;
G, general repeatedly concentrate filtrate merging, separate, promptly.
Realize that the required equipment of aforesaid method comprises:
A, lifting gear generally use 1-2 platform driving, are used for landing solid-phase material and solid-phase material moved to another lixiviate jar from a lixiviate jar;
B, several uncovered chuck lixiviate jars, the dress extraction solvent is used for the lixiviate solid-phase material in jar;
C, with the take away pump that some lixiviate jars link to each other, be used to carry the denseest material that reaches the predetermined color valency to strainer;
D, some mesh bags are used to adorn solid-phase material.
Technical solution of the present invention compared with prior art, maximum difference is to cover and adopt lifting gear to move to another lixiviate jar from a lixiviate jar with mesh bag solid-phase material, in this process, keep vat liquor motionless, vat liquor in that lixiviate jar that immerses solid-phase material first reaches the look value that processing requirement is scheduled to, just liquid material is produced the processing of carrying out subsequent handling to strainer, in a work period, keep the motionless mode of vat liquor owing to this mobile solid-phase material, make a plurality of lixiviate jars form a concentration gradient naturally, gradient lixiviate from big to small successively then, be convenient to continuous production, improve throughput, and obtain the vat liquor of higher concentration easily; Significantly reduced the subsequent disposal amount, saved energy consumption, improved recovery rate, and facility investment is few, simple to operate, the special clean and convenient of solid-liquid discharging has also been stopped the solid materials phenomenon of blocking fully.
The present invention mainly is applicable to the extraction of plant water-soluble pigment, and extraction solvent is water, sour water or buck.
(4) description of drawings
Fig. 1 is the equipment used connection diagram in the technology of the present invention.
1-driving among the figure, 2-lixiviate jar, 3-take away pump, 4-mesh bag.
(5) embodiment:
Embodiment 1
The extraction embodiment of Gardenia Yellow
Figure 406639DEST_PATH_IMAGE001
, according to the characteristic of solid-phase material Gardenia Yellow, with its kernel grain that is ground into 1/16-1/8, getting 100kg, to place the aperture be the mesh bag A of 0.05mm;
B, at No. 1, No. 2 ... the water that to add 600 liters of pH respectively successively in No. 8 lixiviate jars be 6-8 is heated to 40 ℃-55 ℃, and every jar of extraction time is 30 minutes;
C, mesh bag A is put into the lixiviate jar No. 1 by driving, after lixiviate finishes, it is mentioned from the lixiviate jar, above the jar mouth, stopped drop 3-5 minute; It is moved to successively next No. 2, No. 3, No. 4 again ... in No. 8 lixiviate jars, discard the extraction residue;
D, when mesh bag A moves to No. 2 lixiviate jars lixiviate from No. 1 lixiviate jar, inserted the cape jasmine grain of 100kg among the mesh bag B, mesh bag B is inserted in No. 1 lixiviate jar after the lixiviate, take the move mode identical again, move to No. 2, No. 3 of back respectively with mesh bag A ... in No. 8 lixiviate jars; And the like, mesh bag C, mesh bag D, mesh bag E put into the lixiviate jar successively No. 1, and move backward in regular turn by above-mentioned same operation, this moment, the vat liquor look value 〉=500u/ml in No. 1 lixiviate jar emitted the vat liquor in the lixiviate jar No. 1 after testing, filter, filtrate is delivered to the concentrating and separating operation; So far finish a work period;
E, second work period begin, the water that in No. 1 lixiviate jar of vacating, adds the phase isodose earlier, in this work period, each solid-phase material is all since the lixiviate of No. 2 lixiviate jars, and then move to successively No. 3, No. 4 ... No. 8, in No. 1 lixiviate jar, i.e. the lixiviate of solid-phase material is according to the concentration gradient lixiviate from large to small of vat liquor; When the vat liquor look in No. 2 lixiviate jars be worth after testing 〉=500u/ml after, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes second work period;
F, the 3rd work period begin, solid-phase material cape jasmine grain is all since the lixiviate of No. 3 lixiviate jars, and then move to successively No. 4, No. 5 ... No. 8, No. 1, in No. 2 lixiviate jars, when the vat liquor look in No. 3 lixiviate jars be worth after testing 〉=500u/ml after, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes the 3rd work period; Used extraction solvent, extraction time and temperature of above-mentioned each work period be identical with described in the step b all; So circulation continuous gradient lixiviate in each work period, remains solid-phase material vat liquor concentration maximum in that lixiviate jar of submerged first, and newly add that lixiviate jar vat liquor concentration minimum of extraction solvent, circulation cover bubble will meet the requirements of vat liquor and emit successively; The solid-phase material that lixiviate is finished discards;
G, general repeatedly concentrate filtrate merging, separate, and promptly get Gardenia Yellow 18.6kg, and recovery rate is 98.88%.
 
Embodiment 2
The extraction example that sweet potato is red
Figure 229101DEST_PATH_IMAGE001
, according to the characteristic of solid-phase material sweet potato, being cut into thickness is 1-3 millimeter thin slice, getting 100kg, to place the aperture be the mesh bag A of 0.8mm;
B, at No. 1, No. 2 ... the salt sour water that to add 300 liters of pH respectively successively in No. 6 lixiviate jars be 2-2.5, every jar is 25 ℃ of-35 ℃ of following lixiviates 60 minutes;
C, mesh bag A is put into the lixiviate jar No. 1 by driving, after lixiviate finishes, it is mentioned from the lixiviate jar, above the jar mouth, stopped drop 3-5 minute; It is moved to successively next No. 2, No. 3, No. 4 again ... in No. 6 lixiviate jars, discard the extraction residue;
D, when mesh bag A moves to No. 2 lixiviate jars lixiviate from No. 1 lixiviate jar, inserted the sweet potato of 100kg among the mesh bag B, mesh bag B is inserted in No. 1 lixiviate jar after the lixiviate, take the move mode identical again, move to No. 2, No. 3 of back respectively with mesh bag A ... in No. 6 lixiviate jars; And the like, mesh bag C, mesh bag D, mesh bag E put into the lixiviate jar successively No. 1, and move backward in regular turn by above-mentioned same operation, this moment, the vat liquor look value 〉=35u/ml in No. 1 lixiviate jar emitted the vat liquor in the lixiviate jar No. 1 after testing, filter, filtrate is delivered to the concentrating and separating operation; So far finish a work period;
E, second work period begin, the salt sour water that in No. 1 lixiviate jar of vacating, adds the phase isodose earlier, in this work period, each solid-phase material is all since the lixiviate of No. 2 lixiviate jars, and then move to successively No. 3, No. 4 ... No. 6, in No. 1 lixiviate jar, i.e. the lixiviate of solid-phase material is according to the concentration gradient lixiviate from large to small of vat liquor; When the vat liquor look in No. 2 lixiviate jars be worth after testing 〉=35u/ml after, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes second work period;
F, the 3rd work period begin, the solid-phase material sweet potato is all since the lixiviate of No. 3 lixiviate jars, and then move to successively No. 4, No. 5 ... No. 6, No. 1, in No. 2 lixiviate jars, when the vat liquor look in No. 3 lixiviate jars be worth after testing 〉=35u/ml after, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes the 3rd work period; Used extraction solvent, extraction time and temperature of above-mentioned each work period be identical with described in the step b all; So circulation continuous gradient lixiviate, in each work period, remain solid-phase material vat liquor concentration maximum in that lixiviate jar of submerged first, and newly add that lixiviate jar vat liquor concentration minimum of extraction solvent, the circulation cover steeps successively, to meet the requirements of vat liquor and emit, the solid-phase material that lixiviate is finished discards; The solid-phase material that lixiviate is finished discards;
G, general repeatedly concentrate filtrate merging, separate, and promptly get the red 5.2kg of sweet potato, and recovery rate is 98.32%.
 
Embodiment 3
The extraction embodiment of cabbage red
, according to the characteristic of solid-phase material cabbage red, be cut into 1-2 centimetre thread, strip
, getting 100kg, to place the aperture be the mesh bag A of 0.05mm;
B, at No. 1, No. 2 ... the acetic acid water that to add 1000 liters of pH respectively successively in No. 7 lixiviate jars be 2-2.5, under 25 ℃-35 ℃, every jar of extraction time is 60 minutes;
C, mesh bag A is put into the lixiviate jar No. 1 by driving, after lixiviate finishes, it is mentioned from the lixiviate jar, above the jar mouth, stopped drop 3-5 minute; It is moved to successively next No. 2, No. 3, No. 4 again ... in No. 7 lixiviate jars, discard the extraction residue;
D, when mesh bag A moves to No. 2 lixiviate jars lixiviate from No. 1 lixiviate jar, inserted the wild cabbage bar of 100kg among the mesh bag B, mesh bag B is inserted in No. 1 lixiviate jar after the lixiviate, take the move mode identical again, move to No. 2, No. 3 of back respectively with mesh bag A ... in No. 7 lixiviate jars; And the like, mesh bag C, mesh bag D, mesh bag E put into the lixiviate jar successively No. 1, and move backward in regular turn by above-mentioned same operation, this moment, the vat liquor look value 〉=20u/ml in No. 1 lixiviate jar emitted the vat liquor in the lixiviate jar No. 1 after testing, filter, filtrate is delivered to the concentrating and separating operation; So far finish a work period;
E, second work period begin, the acetic acid water that in No. 1 lixiviate jar of vacating, adds the phase isodose earlier, in this work period, each solid-phase material is all since the lixiviate of No. 2 lixiviate jars, and then move to successively No. 3, No. 4 ... No. 7, in No. 1 lixiviate jar, i.e. the lixiviate of solid-phase material is according to the concentration gradient lixiviate from large to small of vat liquor; When the vat liquor look in No. 2 lixiviate jars be worth after testing 〉=20u/ml after, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes second work period;
F, the 3rd work period begin, solid-phase material cape jasmine grain is all since the lixiviate of No. 3 lixiviate jars, and then move to successively No. 4, No. 5 ... No. 7, No. 1, in No. 2 lixiviate jars, when the vat liquor look valency in No. 3 lixiviate jars after testing 〉=20u/ml after, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes the 3rd work period; Used extraction solvent, extraction time and temperature of above-mentioned each work period be identical with described in the step b all; So circulation continuous gradient lixiviate, in each work period, remain solid-phase material vat liquor concentration maximum in that lixiviate jar of submerged first, concentration is successively decreased backward successively, and newly add that lixiviate jar vat liquor concentration minimum of extraction solvent, circulation cover bubble will meet the requirements of vat liquor and emit successively; The solid-phase material that lixiviate is finished discards;
G, general repeatedly concentrate filtrate merging, separate, and promptly get cabbage red 1.86kg, and recovery rate is 99.03%.
Embodiment 4
Sailor yellow extracts embodiment
Figure 632718DEST_PATH_IMAGE001
, according to the characteristic of solid-phase material sailor yellow, it is the mesh bag A of 0.1mm that loose safflower 100kg is placed the aperture;
B, at No. 1, No. 2 ... the water that to add 800 liters of pH respectively successively in No. 7 lixiviate jars be 6-8 is heated to 40 ℃-45 ℃, and every jar of extraction time is 60 minutes;
C, elder generation put into the lixiviate jar with mesh bag A No. 1 by driving, after lixiviate finishes, it are mentioned from the lixiviate jar, stop above the jar mouth drop 3-5 minute; It is moved to successively next No. 2, No. 3, No. 4 again ... in No. 7 lixiviate jars, discard the extraction residue;
D, when mesh bag A moves to No. 2 lixiviate jars lixiviate from No. 1 lixiviate jar, inserted the wild cabbage bar of 100kg among the mesh bag B, mesh bag B is inserted in No. 1 lixiviate jar after the lixiviate, take the move mode identical again, move to No. 2, No. 3 of back respectively with mesh bag A ... in No. 7 lixiviate jars; And the like, mesh bag C, mesh bag D, mesh bag E put into the lixiviate jar successively No. 1, and move backward in regular turn by above-mentioned same operation, this moment, the vat liquor look value 〉=100u/ml in No. 1 lixiviate jar emitted the vat liquor in the lixiviate jar No. 1 after testing, filter, filtrate is delivered to the concentrating and separating operation; So far finish a work period;
E, second work period begin, the water that in No. 1 lixiviate jar of vacating, adds the phase isodose earlier, in this work period, each solid-phase material is all since the lixiviate of No. 2 lixiviate jars, and then moves to successively No. 3, No. 4, No. 5, No. 6, No. 7, in No. 1 lixiviate jar, i.e. the lixiviate of solid-phase material is according to the concentration gradient lixiviate from large to small of vat liquor; When the vat liquor look valency in No. 2 lixiviate jars after testing 〉=100u/ml after, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes second work period;
F, the 3rd work period begin, solid-phase material cape jasmine grain is all since the lixiviate of No. 3 lixiviate jars, and then moves to No. 5 successively No. 4, No. 6, No. 7, No. 1, in No. 2 lixiviate jars, when the vat liquor look valency in No. 3 lixiviate jars after testing 〉=100u/ml after, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes the 3rd work period; Used extraction solvent, extraction time and temperature of above-mentioned each work period be identical with described in the step b all; So circulation continuous gradient lixiviate in each work period, remains solid-phase material vat liquor concentration maximum in that lixiviate jar of submerged first, concentration is successively decreased backward successively, and newly add that lixiviate jar vat liquor concentration minimum of extraction solvent, will meet the requirements of vat liquor to emit; The solid-phase material that lixiviate is finished discards;
G, general repeatedly concentrate filtrate merging, separate, and promptly get sailor yellow 50.6kg, and recovery rate is 98.65%.
Table 1, table 2, table 3 are respectively first work period of embodiment 1-4, second work period and the 3rd work period to finish back lixiviate jar vat liquor concentration gradient table
Figure 239279DEST_PATH_IMAGE002
Figure 2010105828068100002DEST_PATH_IMAGE004
In second, the 3rd production cycle of the foregoing description 1-4, in some jars after second jar, because of being dissolved with certain density extractive substance, therefore, the number of times that immerses solid-phase material is obviously than lacking in first production cycle, the look value that general the immersion 1-2 time, the denseest that jar just can reach regulation can produce and carry out subsequent disposal.

Claims (1)

1. the method for a mobile solid-phase material continuous gradient lixiviate plant water-soluble pigment,
It is characterized in that comprising the steps:
Figure 2010105828068100001DEST_PATH_IMAGE002
, according to the characteristic of solid-phase material, with itself break into meal or cut into slices, bar, place the mesh bag A that adapts with the solid-phase material globule size;
B, at No. 1, No. 2 ... add the extraction solvent of phase isodose in the N lixiviate jar successively respectively, the ratio of extraction solvent and solid-phase material is 3-10:1(V/W); And, adjust suitable pH value according to concrete material properties, and the control solvent temperature is 25-55 ℃, every jar of extraction time is 30-60 minute;
C, mesh bag A is put into the lixiviate jar No. 1 by lifting gear, after lixiviate finishes, it is mentioned from the lixiviate jar, above the jar mouth, stopped drop 3-5 minute; It is moved to successively next No. 2, No. 3, No. 4 again ... in the N lixiviate jar;
D, when mesh bag A moves to No. 2 lixiviate jars lixiviate from No. 1 lixiviate jar, inserted the solid-phase material of isodose mutually among the mesh bag B with mesh bag A, mesh bag B is inserted in No. 1 lixiviate jar after the lixiviate, take the move mode identical again, move to No. 2, No. 3 of back respectively with mesh bag A ... in the N lixiviate jar; And the like, mesh bag C, mesh bag D ... mesh bag N puts into the lixiviate jar successively No. 1, and moves backward in regular turn by above-mentioned same operation, vat liquor look valency in No. 1 lixiviate jar reaches the preset value of processing requirement, emit the vat liquor in the lixiviate jar No. 1, filter, filtrate is delivered to the concentrating and separating operation; So far finish a work period;
E, second work period begin, the extraction solvent that in No. 1 lixiviate jar of vacating, adds the phase isodose earlier, in this work period, each solid-phase material is all since the lixiviate of No. 2 lixiviate jars, and then move to successively No. 3, No. 4 ... N number, in No. 1 lixiviate jar, i.e. the lixiviate of solid-phase material is according to the concentration gradient lixiviate from large to small of vat liquor; After the vat liquor look valency in No. 2 lixiviate jars reaches the processing requirement preset value, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes second work period;
F, the 3rd work period begin, solid-phase material is since the lixiviate of No. 3 lixiviate jars, and then move to successively No. 4, No. 5 ... N number, No. 1, in No. 2 lixiviate jars, after the vat liquor look valency in No. 3 lixiviate jars reaches the processing requirement preset value, emit filtration, filtrate is delivered to the concentrating and separating operation, so far finishes the 3rd work period; Used extraction solvent, extraction time and temperature of above-mentioned each work period be identical with described in the step b all; So circulation continuous gradient lixiviate, in each work period, remain solid-phase material vat liquor concentration maximum in that lixiviate jar of submerged first, and that lixiviate jar that newly adds extraction solvent immerses solid-phase material at last, vat liquor concentration is also minimum, circulation cover bubble will meet the requirements of vat liquor and emit successively, and the solid-phase material that lixiviate is finished discards;
G, general repeatedly concentrate filtrate merging, separate, promptly.
CN2010105828068A 2010-12-10 2010-12-10 Method for digesting plant water-soluble pigment from mobile solid phase material in continuous gradient manner Pending CN102061105A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2010105828068A CN102061105A (en) 2010-12-10 2010-12-10 Method for digesting plant water-soluble pigment from mobile solid phase material in continuous gradient manner

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010105828068A CN102061105A (en) 2010-12-10 2010-12-10 Method for digesting plant water-soluble pigment from mobile solid phase material in continuous gradient manner

Publications (1)

Publication Number Publication Date
CN102061105A true CN102061105A (en) 2011-05-18

Family

ID=43996616

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2010105828068A Pending CN102061105A (en) 2010-12-10 2010-12-10 Method for digesting plant water-soluble pigment from mobile solid phase material in continuous gradient manner

Country Status (1)

Country Link
CN (1) CN102061105A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106512467A (en) * 2015-09-13 2017-03-22 王建卫 Economical solid-liquid transfer method

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4204043A (en) * 1978-04-04 1980-05-20 The United States Of America As Represented By The Secretary Of Agriculture Method of removing pigment from annatto seed
CN1664017A (en) * 2005-03-28 2005-09-07 浙江省农业科学院 Process for extracting natural pigment
CN1912011A (en) * 2005-08-11 2007-02-14 青岛海联植物科技研究所 Method for extracting matural dye from external skin of walnut
CN101028065A (en) * 2007-03-30 2007-09-05 王克俭 Extraction of purplish natural pigment

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4204043A (en) * 1978-04-04 1980-05-20 The United States Of America As Represented By The Secretary Of Agriculture Method of removing pigment from annatto seed
CN1664017A (en) * 2005-03-28 2005-09-07 浙江省农业科学院 Process for extracting natural pigment
CN1912011A (en) * 2005-08-11 2007-02-14 青岛海联植物科技研究所 Method for extracting matural dye from external skin of walnut
CN101028065A (en) * 2007-03-30 2007-09-05 王克俭 Extraction of purplish natural pigment

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
蔺定运: "《食用色素的识别及应用》", 30 June 1987, article "《食用色素的识别及应用》", pages: 108-109 *
马自超等: "《天然食用色素化学及生产工艺学》", 30 September 1994, article "天然食用色素化学及生产工艺", pages: 182 - 187 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106512467A (en) * 2015-09-13 2017-03-22 王建卫 Economical solid-liquid transfer method

Similar Documents

Publication Publication Date Title
CN108383886B (en) Method for extracting hesperidin from immature bitter orange by continuous countercurrent method and hesperidin obtained by extraction
EP3798201A1 (en) Device for preparing xylitol by integrating evaporation, crystallization and centrifugal separation, and control method therefor
CN104447944A (en) Extracting method of grape seed protein
CN105175564A (en) Industrial extraction and separation method of ganoderma spore polysaccharide and separation device
CN203872952U (en) Pepper rind and seed separating device
CN102061105A (en) Method for digesting plant water-soluble pigment from mobile solid phase material in continuous gradient manner
CN103864945B (en) A kind of method strengthening polysaccharide in extraction Cordyceps militaris rice medium
CN101805621B (en) Grease producing method and grease leacher
CN105950277B (en) A kind of mountain almond oil extraction refinery practice
CN105670336B (en) A kind of technique from the cape jasmine highly purified Gardenia Yellow of fruit high efficiency extraction
CN210008482U (en) Vacuum sugaring production and processing device for passion fruits
CN107087798B (en) Grape juice apparatus for producing
CN102766525B (en) Method for squeezing tea seed oil at normal temperature
CN108949523A (en) A kind of technique and system of industrialized production glycosylglycerol
CN209967740U (en) Geniposide microwave extraction device
JP6063169B2 (en) Method for producing plant extract
CN102827308A (en) Method for purifying extract in inulin production through membrane process
CN102766527A (en) Method for squeezing and refining tea seed oil at low temperature
CN110357974A (en) A kind of method of the quick slurry separation of pueraria starch
CN106666066A (en) Ultrasonic extraction method for sunflower seed protein
CN106727835A (en) A kind of alkalescent wine extracts active ingredients from traditional Chinese medicinal process
CN104997135A (en) Peanut sheller
CN214339852U (en) Production device of selenium-rich tea extract
CN220812322U (en) Zanthoxylum oil production system
CN104719991A (en) Device for peeling tentacles of squid employing enzymic method

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20110518