CN104357591A - Process for producing feed-grade xylo-oligosaccharide from viscose fiber squeezed alkali liquor - Google Patents

Process for producing feed-grade xylo-oligosaccharide from viscose fiber squeezed alkali liquor Download PDF

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Publication number
CN104357591A
CN104357591A CN201410622263.6A CN201410622263A CN104357591A CN 104357591 A CN104357591 A CN 104357591A CN 201410622263 A CN201410622263 A CN 201410622263A CN 104357591 A CN104357591 A CN 104357591A
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China
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oligosaccharide
membrane
viscose fiber
xylo
technique
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Inventor
邓传东
冯涛
孙毅
唐孝兵
莫世清
周林
罗红梅
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Yibin Grace Group Co Ltd
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YIBIN YATAI BIOTECHNOLOGY Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C13SUGAR INDUSTRY
    • C13KSACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
    • C13K13/00Sugars not otherwise provided for in this class
    • C13K13/002Xylose

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Organic Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

The invention provides a process for producing feed-grade xylo-oligosaccharide from viscose fiber squeezed alkali liquor. The process comprises the following specific process steps: (A) carrying out membrane concentration: firstly pre-filtering squeezed liquor for viscose fiber production, so as to remove large-granule impurities, cyclically concentrating the permeate for 2-4 times with a nano-filtration membrane, thinning up the finally-concentrated concentrate with water, and filtrating with a ceramic membrane, so as to obtain a concentrate, namely a concentrate of the squeezed alkali liquor, wherein during the 2-4 times of cyclic concentrating of the nano-filtration membrane, before every filtration, material liquid is thinned up with water and then enters the nano-filtration membrane; (B) extracting hemicellulose: adding acid to neutralize the concentrate of the squeezed alkali liquor, so as to obtain hemicellulose liquid; (C) carrying out enzymolysis: adding a compound enzyme into the hemicellulose liquid, and carrying out enzymolysis reaction, so as to obtain an enzymolysis solution; (D) purifying: filtrating the enzymolysis solution with the ceramic membrane, desalting the permeate with the nano-filtration membrane, so as to obtain a concentrate, namely a purified solution of xylo-oligosaccharide, evaporating and baking, thereby obtaining the feed-grade xylo-oligosaccharide.

Description

With the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide
Technical field
The present invention relates to xylo-oligosaccharide preparation field, be specifically related to the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide.
Background technology
Xylo-oligosaccharide, also known as wood oligose, is the general name of the IMO be combined into β-Isosorbide-5-Nitrae-glycosidic link by 2-7 wood sugar.Effective constituent is xylo-bioses, xylotriose, Xylotetrose, wooden pentasaccharides etc., wherein based on xylo-bioses and xylotriose.Have unique advantage compared with soybean oligosaccharide, oligofructose, oligomeric isomaltose etc. that xylo-oligosaccharide is used with usual people, it optionally can promote the proliferation activity of intestinal bifidobacteria, and its bifidobacterium factor functional is 10-20 times of other polymerization carbohydrate.Xylo-oligosaccharide is considered to desirable protective foods sweeting agent because of advantages such as its significant bifidus bacillus multiplication capacity, decomposition difficult to digest, low carious tooth, effectively intake are few, and its acidproof heat-proof also makes it be applied to the industries such as medicine, beverage, fodder additives simultaneously.
Xylo-oligosaccharide, to be rich in the plant of xylan for raw material, is produced by biochemical method.The production of current xylo-oligosaccharide is raw material mainly with corn cob, and complex manufacturing, cost is higher.And at chemical pulp plant celluloses such as () wood pulp, cotton pulp, straw pulp, reed pulps in the production process of viscose fiber of raw material, adopting alkali lye to process (dipping, squeezing) to Mierocrystalline cellulose is the first step manufacturing viscose fiber.Hemicellulose concentration is high, extremely adverse influence is produced to cellulose viscose manufacturing technique and final product quality, therefore must in impregnation technology with alkali lye by hemicellulose stripping, the Mierocrystalline cellulose of high strength could be obtained, so a large amount of high concentration alkali pressed liquors being rich in hemicellulose can be produced in above process.
Main component in alkali pressed liquor is sodium hydroxide and hemicellulose.Hemicellulose is therefrom separated by treatment process many employings nanofiltration of existing press lye, obtains comparatively pure alkali lye.Through purification alkali lye can direct reuse in technique, but part alkali only can be realized reuse by nanofiltration membrane, still containing a large amount of alkali in the concentrated solution that the hemicellulose in its trapped fluid obtains after concentrated.During at present this part feed liquid is used for as salkali waste and technique, hemicellulose enters wastewater treatment, or adopts calcination to reclaim sodium hydroxide, and hemicellulose is burned.From above existing technique, hemicellulose is not fully used.
Document " the membrane separation concentration technical study of xylo-oligosaccharide " (" foodstuffs industry ", 09 phase in 2012), pilot plant test device is adopted to carry out pilot plant test to the separation of lower concentration xylo-oligosaccharide solution is concentrated, the effect of the polyamide-based nanofiltration of comparative studies and reverse osmosis two kinds of membrane techniquies, determines the optimised process operational condition that nanofiltration membrane separation concentrates xylo-oligosaccharide solution.This technique nanofiltration membrane thickening temperature is low, and membrane filtration efficiency is lower, is unsuitable for industrialization scale operation.
Summary of the invention
For above-mentioned technical problem, the invention provides with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide.The xylo-oligosaccharide salinity obtained is low, and purity is high, and process operation efficiency is high, is adapted to scale operation.
For achieving the above object, the present invention adopts following technical scheme:
With the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: concrete technology step is as follows:
A, membrane concentration
The press lye produced by viscose fiber is first after pre-filtering removing large granular impurity, enter ultrafiltration membrane treatment, permeate is through concentrated 2-4 time of nanofiltration membrane circulation, and send after last concentrated solution thin up into ceramic membrane filter, gained concentrated solution is the concentrated solution of press lye; Concentrated 2-4 time of described nanofiltration membrane circulation, before each filtration, feed liquid all enters nanofiltration membrane after thin up.
B, extraction half fibre
By the concentrated solution acid neutralization of press lye, obtain half fine liquid.
C, enzymolysis
In half fine liquid, add prozyme, enzyme digestion reaction occurs and obtains enzymolysis solution;
D, purification
Enzymolysis solution is through ceramic membrane filter, and permeate enters nanofiltration membrane desalination, and gained concentrated solution is the refined solution of xylo-oligosaccharide, then obtains feed grade xylo-oligosaccharide through evaporation, oven dry.
The xylo-oligosaccharide that preparation method of the present invention obtains meets the national standard GB/T 23747-2009 of feed grade xylo-oligosaccharide.
Step A of the present invention, ultra-filtration membrane molecular weight cut-off is 10000-15000, and the molecular weight cut-off of described nanofiltration membrane is 200-400, and the molecular weight cut-off of ceramic membrane is 800-1500.
Ultrafiltration membrance filter amount is large, is conducive to improving filtration efficiency; The molecular weight cut-off of 200-400, makes alkali separate from permeate, progressively lowers alkali dense, promotes half fine concentration, retain a part of monose simultaneously; The molecular weight cut-off of ceramic membrane is 800-1500, can retain half fibre, improve the purity of product.
Step A of the present invention, before each nanofiltration membrane, the amount of thin up is 1 times of stock liquid volume, filters the concentrated solution volume obtained identical with stock liquid volume.While ensureing filtration efficiency, little to the damage of nanofiltration membrane.
Preferably, described permeate, containing alkali 200-300g/l, containing half fine 40-80 g/l, after nanofiltration membrane circulation is concentrated, obtains concentrated solution containing alkali 12-75g/l, containing half fine 40-80g/l.Under lowering the dense prerequisite of alkali, ensure the filtration efficiency of film.
Step A of the present invention, feed liquid first enters ceramic membrane device through thin up, and add water to feed liquid gradation in working cycle, total amount of water is 5 times of material liquid volume, and gained concentrated solution volume is identical with stock liquid volume.While ensureing filtration efficiency, little to the damage of ceramic membrane.
Preferably, containing alkali 2-4g/l in the concentrated solution of described ceramic membrane filter, containing half fine 40-80 g/l.Be down to minimum by dense for alkali, ensure that the purity of half fibre.
Pre-filtering of the present invention refers to, press lye filters and Plate Filtration removing large granular impurity through rotary drum successively.Pre-filtering makes press lye not containing the solid impurity of more than 5 microns, and protection film is not below damaged by solid impurity.
Step A of the present invention, the temperature of ultrafiltration is 30-40 DEG C, and the temperature of nanofiltration membrane is 40-60 DEG C, and the temperature of ceramic membrane filter is 60-80 DEG C, and filtration temperature is high, and liquid viscosity is lower, is conducive to filtration efficiency and improves.
Step A of the present invention, the mistake mould difference of ultrafiltration is 2-3bar, and the mistake mould difference of nanofiltration membrane is 3-4bar, and the mistake mould difference of ceramic membrane is 5-6bar.For the feature that viscose glue press lye viscosity is higher, adopt higher pressure reduction to filter, can ensure that half fine concentration in alkali lye reaches processing requirement.
Step A of the present invention, feed liquid is 60-80 m at the flow of ultra-filtration membrane 3/ h, the flow in nanofiltration membrane is 25-40m 3/ h, the flow in ceramic membrane is 200-250m 3/ h.The surface velocity that bonding props up film is higher, film is not easy contaminated.
Step A of the present invention, it is 26.8m that the list of ultra-filtration membrane props up filtration area 2, it is 26.8m that the list of nanofiltration membrane props up filtration area 2, it is 0.6m that the list of ceramic membrane props up filtration area 2, single film has larger filtration area under the prerequisite taking less space.
Step B of the present invention, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 4-5.The advantage adding hydrochloric acid is that the molecules of salt amount formed is lower, and be conducive to the desalination in later stage, pH value is 4-5, adapts to the pH value requirement of enzymolysis.
Step C of the present invention, prozyme is zytase, cellulase and polygalacturonase, can improve sugared associative key susceptibility to enzymic hydrolysis after adding appropriate cellulase and pectin in zytase.
Preferably, the ratio of described zytase, cellulase and polygalacturonase is 3:2:1, and adopt the prozyme of this ratio to carry out degrading and can make the maximum production of xylo-oligosaccharide, the percent hydrolysis of hemicellulose is up to more than 95%.
Preferably, the enzymolysis time of described enzyme digestion reaction is 0.5-2h, and temperature is 50-60 DEG C, and the pH value of enzyme digestion reaction is 4-5, and under this condition, the activity of enzyme is the highest.
Preferably, the enzyme concentration of described enzyme digestion reaction is 0.5-1.5%, and now the catalytic effect of enzyme is best.
D step of the present invention, the molecular weight cut-off of ceramic membrane is 800-1500, and separating oligomeric wood sugar and undegradable half fibre, ensure product purity.
D step of the present invention, the molecular weight cut-off of described nanofiltration membrane is 100-200.Owing to adopting hydrochloric acid neutralization, the salt of generation is sodium-chlor, and the molecular weight of sodium-chlor is smaller, and far below 100, and xylo-oligosaccharide molecular weight is much larger than 100, effectively can realize being separated of salt and xylo-oligosaccharide.
Preferably, described nanofiltration membrane desalination, crossing mould difference is 3-4bar, and temperature is 30-40 DEG C, and single filtration area is 26.8 m 2, adapt to the change of low catching molecular, guarantee salt is separated with xylo-oligosaccharide.
Preferably, the material liquid volume before described nanofiltration membrane concentrates is 10-15 times of concentrated solution volume, is conducive to reducing the salt content in xylo-oligosaccharide.
Beneficial effect of the present invention is:
1, the present invention adopts ultra-filtration membrane, nanofiltration membrane and ceramic membrane to combine filtering and concentrating half fibre, because the filtration efficiency of ultrafiltration and nanofiltration is higher than ceramic membrane, first with the macro-molecular protein in ultrafiltration membrance filter removal alkali lye and bacterium, adopt repeatedly nanofiltration membrane that alkali concn is progressively dropped to certain degree again, concentrated half fibre simultaneously, reduce the damage to film, then adopt ceramic membrane filter; The feed liquid that ceramic membrane is applicable to filter the dense height of later stage low alkali half fine is run, and is the powerful guarantee that low alkali is dense.Nanofiltration membrane and ceramic membrane cooperatively interact, and have complementary advantages, and make containing alkali 2-4g/l in final concentrated solution, containing half fine 40-80 g/l, achieve low alkali dense, height half is fine; And process operation efficiency is high, little to the damage of film, cost is low.
2, the amount of nanofiltration membrane thin up of the present invention is 1 times of stock liquid volume, filters the concentrated solution volume obtained identical with stock liquid volume at every turn, can realize nanofiltration membrane water 10m excessively per hour 3left and right, ensure that filtration efficiency; Meanwhile, little to the damage of film, the 2-3 that can reach its quality guarantee period work-ing life doubly, reduces cost to a great extent, is adapted to industrialization scale operation.
3, the present invention adds hydrochloric acid neutralization to the concentrated solution obtained, then adopts molecular weight cut-off to be the nanofiltration membrane desalination of 100-200.In hydrochloric acid and the salt generated be sodium-chlor, the molecular weight of sodium-chlor, far below 100, and xylo-oligosaccharide molecular weight is much larger than 100, effectively can realize being separated of salt and xylo-oligosaccharide.Be conducive to the desalination in later stage, further increase the purity of xylo-oligosaccharide.
4, enzymolysis solution is first used ceramic membrane separation xylo-oligosaccharide and undegradable half fibre by the present invention, ensure product purity, permeate enters nanofiltration membrane desalination again, thus have effectively achieved being separated of salt and xylo-oligosaccharide, the specific conductivity finally obtaining xylo-oligosaccharide is 8000-10000 μ s/cm, and ignition residue is 3-6%.Ignition residue is the direct indicator weighing inorganic salt, and the massfraction described in xylo-oligosaccharide shared by inorganic salt is only 3-6%; Specific conductivity is the electrolytical degree existed in reaction liquid, and the main electrolyte of xylo-oligosaccharide is exactly inorganic salts, so this index also can reflect the number of salinity in product.It is low that low conductivity and ignition residue describe the xylo-oligosaccharide salinity adopting the inventive method to obtain, high purity more than 80%.
Embodiment
Below in conjunction with embodiment, essentiality content of the present invention is described in further detail.
Embodiment 1
With the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, concrete technology step is as follows:
A, membrane concentration
The press lye produced by viscose fiber is first after pre-filtering removing large granular impurity, enter ultrafiltration membrane treatment, permeate is through concentrated 2 times of nanofiltration membrane circulation, and send after last concentrated solution thin up into ceramic membrane filter, gained concentrated solution is the concentrated solution of press lye; Concentrated 2 times of described nanofiltration membrane circulation, before each filtration, feed liquid all enters nanofiltration membrane after thin up.
B, extraction half fibre
By the concentrated solution acid neutralization of press lye, obtain half fine liquid.
C, enzymolysis
In half fine liquid, add prozyme, enzyme digestion reaction occurs and obtains enzymolysis solution;
D, purification
Enzymolysis solution is through ceramic membrane filter, and permeate enters nanofiltration membrane desalination, and gained concentrated solution is the refined solution of xylo-oligosaccharide, then obtains feed grade xylo-oligosaccharide through evaporation, oven dry.
Embodiment 2
With the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, concrete technology step is as follows:
A, membrane concentration
The press lye produced by viscose fiber is first after pre-filtering removing large granular impurity, enter ultrafiltration membrane treatment, permeate is through concentrated 3 times of nanofiltration membrane circulation, and send after last concentrated solution thin up into ceramic membrane filter, gained concentrated solution is the concentrated solution of press lye; Concentrated 3 times of described nanofiltration membrane circulation, before each filtration, feed liquid all enters nanofiltration membrane after thin up.
B, extraction half fibre
By the concentrated solution acid neutralization of press lye, obtain half fine liquid.
C, enzymolysis
In half fine liquid, add prozyme, enzyme digestion reaction occurs and obtains enzymolysis solution;
D, purification
Enzymolysis solution is through ceramic membrane filter, and permeate enters nanofiltration membrane desalination, and gained concentrated solution is the refined solution of xylo-oligosaccharide, then obtains feed grade xylo-oligosaccharide through evaporation, oven dry.
Embodiment 3
With the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, concrete technology step is as follows:
A, membrane concentration
The press lye produced by viscose fiber is first after pre-filtering removing large granular impurity, enter ultrafiltration membrane treatment, permeate is through concentrated 4 times of nanofiltration membrane circulation, and send after last concentrated solution thin up into ceramic membrane filter, gained concentrated solution is the concentrated solution of press lye; Concentrated 4 times of described nanofiltration membrane circulation, before each filtration, feed liquid all enters nanofiltration membrane after thin up.
B, extraction half fibre
By the concentrated solution acid neutralization of press lye, obtain half fine liquid.
C, enzymolysis
In half fine liquid, add prozyme, enzyme digestion reaction occurs and obtains enzymolysis solution;
D, purification
Enzymolysis solution is through ceramic membrane filter, and permeate enters nanofiltration membrane desalination, and gained concentrated solution is the refined solution of xylo-oligosaccharide, then obtains feed grade xylo-oligosaccharide through evaporation, oven dry.
Embodiment 4
The present embodiment is substantially the same manner as Example 1, on this basis:
Described step A, ultra-filtration membrane molecular weight cut-off is 10000, and the molecular weight cut-off of nanofiltration membrane is 200, and the molecular weight cut-off of ceramic membrane is 800.
The nanofiltration membrane circulation of described step A is concentrated, and the amount of thin up is 1 times of stock liquid volume, filters the concentrated solution volume obtained identical with stock liquid volume at every turn.
Embodiment 5
The present embodiment is substantially the same manner as Example 2, on this basis:
Described step A, ultra-filtration membrane molecular weight cut-off is 15000, and the molecular weight cut-off of nanofiltration membrane is 400, and the molecular weight cut-off of ceramic membrane is 1500.
The nanofiltration membrane circulation of described step A is concentrated, and the amount of thin up is 1 times of stock liquid volume, filters the concentrated solution volume obtained identical with stock liquid volume at every turn.
Embodiment 6
The present embodiment is substantially the same manner as Example 3, on this basis:
Described step A, ultra-filtration membrane molecular weight cut-off is 12000, and the molecular weight cut-off of nanofiltration membrane is 300, and the molecular weight cut-off of ceramic membrane is 1000.
The nanofiltration membrane circulation of described step A is concentrated, and the amount of thin up is 1 times of stock liquid volume, filters the concentrated solution volume obtained identical with stock liquid volume at every turn.
Embodiment 7
The present embodiment is substantially the same manner as Example 1, on this basis:
Described step A, ultra-filtration membrane molecular weight cut-off is 11000, and the molecular weight cut-off of nanofiltration membrane is 250, and the molecular weight cut-off of ceramic membrane is 900.
The nanofiltration membrane circulation of described step A is concentrated, and the amount of thin up is 1 times of stock liquid volume, filters the concentrated solution volume obtained identical with stock liquid volume at every turn.
Embodiment 8
The present embodiment is substantially the same manner as Example 4, on this basis:
Described step A, permeate, containing alkali 300g/l, containing half fine 80g/l, after nanofiltration membrane circulation is concentrated, obtains concentrated solution containing alkali 75g/l, containing half fine 80g/l.
Embodiment 9
The present embodiment is substantially the same manner as Example 5, on this basis:
Described step A, permeate, containing alkali 260g/l, containing half fine 70g/l, after nanofiltration membrane circulation is concentrated, obtains concentrated solution containing alkali 32.5g/l, containing half fine 80g/l.
Embodiment 10
The present embodiment is substantially the same manner as Example 6, on this basis:
Described step A, permeate, containing alkali 200g/l, containing half fine 40g/l, after nanofiltration membrane circulation is concentrated, obtains concentrated solution containing alkali 12.5g/l, containing half fine 40g/l.
Embodiment 11
The present embodiment is substantially the same manner as Example 7, on this basis:
Described step A, permeate, containing alkali 220g/l, containing half fine 60g/l, after nanofiltration membrane circulation is concentrated, obtains concentrated solution containing alkali 55g/l, containing half fine 60g/l.
Embodiment 12
The present embodiment is substantially the same manner as Example 8, on this basis:
The ceramic membrane filter of described step A, feed liquid first enters ceramic membrane device through thin up, and add water to feed liquid gradation in working cycle, total amount of water is 5 times of material liquid volume, and gained concentrated solution volume is identical with stock liquid volume.
Described step A, containing alkali 2g/l in the concentrated solution of ceramic membrane filter, containing half fine 40g/l.
Described pre-filtering refers to, pressed liquor filters and Plate Filtration removing large granular impurity through rotary drum successively.
Embodiment 13
The present embodiment is substantially the same manner as Example 9, on this basis:
The ceramic membrane filter of described step A, feed liquid first enters ceramic membrane device through thin up, and add water to feed liquid gradation in working cycle, total amount of water is 5 times of material liquid volume, and gained concentrated solution volume is identical with stock liquid volume.
Described step A, containing alkali 4g/l in the concentrated solution of ceramic membrane filter, containing half fine 80 g/l.
Described pre-filtering refers to, pressed liquor filters and Plate Filtration removing large granular impurity through rotary drum successively.
Described step A, the temperature of ultrafiltration is 30 DEG C, and the temperature of nanofiltration membrane is 40 DEG C, and the temperature of ceramic membrane filter is 60 DEG C.
Embodiment 14
The present embodiment is substantially the same manner as Example 10, on this basis:
The ceramic membrane filter of described step A, feed liquid first enters ceramic membrane device through thin up, and add water to feed liquid gradation in working cycle, total amount of water is 5 times of material liquid volume, and gained concentrated solution volume is identical with stock liquid volume.
Described step A, containing alkali 3g/l in the concentrated solution of ceramic membrane filter, containing half fine 50g/l.
Described pre-filtering refers to, pressed liquor filters and Plate Filtration removing large granular impurity through rotary drum successively.
Described step A, the temperature of ultrafiltration is 40 DEG C, and the temperature of nanofiltration membrane is 60 DEG C, and the temperature of ceramic membrane filter is 80 DEG C.
Described step A, the mistake mould difference of ultrafiltration is 3bar, and the mistake mould difference of nanofiltration membrane is 4bar, and the mistake mould difference of ceramic membrane is 6bar.
Embodiment 15
The present embodiment is substantially the same manner as Example 11, on this basis:
The ceramic membrane filter of described step A, feed liquid first enters ceramic membrane device through thin up, and add water to feed liquid gradation in working cycle, total amount of water is 5 times of material liquid volume, and gained concentrated solution volume is identical with stock liquid volume.
Described step A, containing alkali 2.5g/l in the concentrated solution of ceramic membrane filter, containing half fine 60g/l.
Described pre-filtering refers to, pressed liquor filters and Plate Filtration removing large granular impurity through rotary drum successively.
Described step A, the temperature of ultrafiltration is 35 DEG C, and the temperature of nanofiltration membrane is 45 DEG C, and the temperature of ceramic membrane filter is 65 DEG C.
The mistake mould difference of described ultrafiltration is 2bar, and the mistake mould difference of nanofiltration membrane is 3bar, and the mistake mould difference of ceramic membrane is 5bar.
Described step A, feed liquid is 60m at the flow of ultra-filtration membrane 3/ h, the flow in nanofiltration membrane is 25m 3/ h, the flow in ceramic membrane is 200m 3/ h.
Embodiment 16
The present embodiment is substantially the same manner as Example 11, on this basis:
The ceramic membrane filter of described step A, feed liquid first enters ceramic membrane device through thin up, and add water to feed liquid gradation in working cycle, total amount of water is 5 times of material liquid volume, and gained concentrated solution volume is identical with stock liquid volume.
Described step A, containing alkali 3.5g/l in the concentrated solution of ceramic membrane filter, containing half fine 70g/l.
Described pre-filtering refers to, pressed liquor filters and Plate Filtration removing large granular impurity through rotary drum successively.
Described step A, the temperature of ultrafiltration is 32 DEG C, and the temperature of nanofiltration membrane is 55 DEG C, and the temperature of ceramic membrane filter is 75 DEG C.
Described step A, the mistake mould difference of ultrafiltration is 2.5bar, and the mistake mould difference of nanofiltration membrane is 3.6bar, and the mistake mould difference of ceramic membrane is 5.6bar.
Described step A, feed liquid is 80m at the flow of ultra-filtration membrane 3/ h, the flow in nanofiltration membrane is 40m 3/ h, the flow in ceramic membrane is 250m 3/ h.
Described step A, it is 26.8m that the list of ultra-filtration membrane props up filtration area 2, it is 26.8m that the list of nanofiltration membrane props up filtration area 2, it is 0.6m that the list of ceramic membrane props up filtration area 2.
Embodiment 17
The present embodiment is substantially the same manner as Example 11, on this basis:
The ceramic membrane filter of described step A, feed liquid first enters ceramic membrane device through thin up, and add water to feed liquid gradation in working cycle, total amount of water is 5 times of material liquid volume, and gained concentrated solution volume is identical with stock liquid volume.
Described step A, containing alkali 3.8g/l in the concentrated solution of ceramic membrane filter, containing half fine 65g/l.
Described pre-filtering refers to, pressed liquor filters and Plate Filtration removing large granular impurity through rotary drum successively.
Described step A, the temperature of ultrafiltration is 32 DEG C, and the temperature of nanofiltration membrane is 55 DEG C, and the temperature of ceramic membrane filter is 72 DEG C.
Described step A, the mistake mould difference of ultrafiltration is 2.6bar, and the mistake mould difference of nanofiltration membrane is 3.6bar, and the mistake mould difference of ceramic membrane is 5.2bar.
Described step A, feed liquid is 65m at the flow of ultra-filtration membrane 3/ h, the flow in nanofiltration membrane is 30m 3/ h, the flow in ceramic membrane is 220m 3/ h.
Described step A, it is 26.8m that the list of nanofiltration membrane props up filtration area 2, it is 0.6m that the list of ceramic membrane props up filtration area 2.
Embodiment 18
The present embodiment is substantially the same manner as Example 8, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 4.
Embodiment 19
The present embodiment is substantially the same manner as Example 9, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 5.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
Embodiment 20
The present embodiment is substantially the same manner as Example 10, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 4.5.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
The enzymolysis time of described enzyme digestion reaction is 0.5h, and temperature is 60 DEG C, and the pH value of enzyme digestion reaction is 4.5.
Embodiment 21
The present embodiment is substantially the same manner as Example 11, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 4.6.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
The enzymolysis time of described enzyme digestion reaction is 2h, and temperature is 50 DEG C, and the pH value of enzyme digestion reaction is 4.6.
The enzyme concentration of described enzyme digestion reaction is 0.5%.
Embodiment 22
The present embodiment is substantially the same manner as Example 16, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value 4.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
The enzymolysis time of described enzyme digestion reaction is 1h, and temperature is 52 DEG C, and the pH value of enzyme digestion reaction is 4.
The enzyme concentration of described enzyme digestion reaction is 1.5%.
Described D step, the molecular weight cut-off of ceramic membrane is 800.
Embodiment 23
The present embodiment is substantially the same manner as Example 17, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 5.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
The enzymolysis time of described enzyme digestion reaction is 1.5h, and temperature is 55 DEG C, and the pH value of enzyme digestion reaction is 5.
The enzyme concentration of described enzyme digestion reaction is 1%.
Described D step, the molecular weight cut-off of ceramic membrane is 1500.
Described D step, the molecular weight cut-off of nanofiltration membrane is 200.
Embodiment 24
The present embodiment is substantially the same manner as Example 17, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 4.2.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
The enzymolysis time of described enzyme digestion reaction is 0.6h, and temperature is 52 DEG C, and the pH value of enzyme digestion reaction is 4.2.
The enzyme concentration of described enzyme digestion reaction is 0.6%.
Described D step, the molecular weight cut-off of ceramic membrane is 1000.
Described D step, the molecular weight cut-off of nanofiltration membrane is 100.
The mistake mould difference of described nanofiltration membrane is 3bar, and temperature is 30 DEG C, and single filtration area is 26.8 m 2.
Embodiment 25
The present embodiment is substantially the same manner as Example 17, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 4.5.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
The enzymolysis time of described enzyme digestion reaction is 1.5h, and temperature is 58 DEG C, and the pH value of enzyme digestion reaction is 4.5.
The enzyme concentration of described enzyme digestion reaction is 0.8%.
Described D step, the molecular weight cut-off of ceramic membrane is 900.
Described D step, the molecular weight cut-off of nanofiltration membrane is 120.
The mistake mould difference of described nanofiltration membrane is 4bar, and temperature is 40 DEG C, and single filtration area is 26.8 m 2.
Described D step, the material liquid volume before nanofiltration membrane concentrates is 10 times of concentrated solution volume.
The specific conductivity obtaining xylo-oligosaccharide is 9500 μ s/cm, and ignition residue is 5.5%.
Embodiment 26
The present embodiment is substantially the same manner as Example 17, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 4.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
The enzymolysis time of described enzyme digestion reaction is 0.7h, and temperature is 52 DEG C, and the pH value of enzyme digestion reaction is 4.
The enzyme concentration of described enzyme digestion reaction is 0.8%.
Described D step, the molecular weight cut-off of ceramic membrane is 950.
Described D step, the molecular weight cut-off of nanofiltration membrane is 150.
The mistake mould difference of described nanofiltration membrane is 3.5bar, and temperature is 32 DEG C, and single filtration area is 26.8 m 2.
Described D step, the material liquid volume before nanofiltration membrane concentrates is 15 times of concentrated solution volume.
The specific conductivity obtaining xylo-oligosaccharide is 8500 μ s/cm, and ignition residue is 4%.
Embodiment 27
The present embodiment is substantially the same manner as Example 17, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 5.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
The enzymolysis time of described enzyme digestion reaction is 2h, and temperature is 56 DEG C, and the pH value of enzyme digestion reaction is 5.
The enzyme concentration of described enzyme digestion reaction is 1.2%.
Described D step, the molecular weight cut-off of ceramic membrane is 1200.
Described D step, the molecular weight cut-off of nanofiltration membrane is 180.
The mistake mould difference of described nanofiltration membrane is 3.6bar, and temperature is 35 DEG C, and single filtration area is 26.8 m 2.
Described D step, the material liquid volume before nanofiltration membrane concentrates is 12 times of concentrated solution volume.
The specific conductivity obtaining xylo-oligosaccharide is 9000 μ s/cm, and ignition residue is 5%.
Embodiment 28
The present embodiment is substantially the same manner as Example 17, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 4.3.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
The enzymolysis time of described enzyme digestion reaction is 0.9h, and temperature is 53 DEG C, and the pH value of enzyme digestion reaction is 4.3.
The enzyme concentration of described enzyme digestion reaction is 1.1%.
Described D step, the molecular weight cut-off of ceramic membrane is 800.
Described D step, the molecular weight cut-off of nanofiltration membrane is 105.
The mistake mould difference of described nanofiltration membrane is 3.6bar, and temperature is 36 DEG C, and single filtration area is 26.8 m 2.
Described D step, the material liquid volume before nanofiltration membrane concentrates is 13 times of concentrated solution volume.
The specific conductivity obtaining xylo-oligosaccharide is 10000 μ s/cm, and ignition residue is 6%.
Embodiment 29
The present embodiment is substantially the same manner as Example 17, on this basis:
Described step B, concentrated solution acid neutralization, refers to and adds hydrochloric acid neutralization, make pH value be 4.5.
Described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
The enzymolysis time of described enzyme digestion reaction is 1.5h, and temperature is 56 DEG C, and the pH value of enzyme digestion reaction is 4.5.
The enzyme concentration of described enzyme digestion reaction is 0.8%.
Described D step, the molecular weight cut-off of ceramic membrane is 1000.
Described D step, the molecular weight cut-off of nanofiltration membrane is 120.
The mistake mould difference of described nanofiltration membrane is 3bar, and temperature is 32 DEG C, and single filtration area is 26.8 m 2.
Described D step, the material liquid volume before nanofiltration membrane concentrates is 12 times of concentrated solution volume.
The specific conductivity obtaining xylo-oligosaccharide is 8000 μ s/cm, and ignition residue is 3%.

Claims (18)

1. with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: concrete technology step is as follows:
A, membrane concentration
The press lye produced by viscose fiber is first after pre-filtering removing large granular impurity, enter ultrafiltration membrane treatment, permeate is through concentrated 2-4 time of nanofiltration membrane circulation, and send after last concentrated solution thin up into ceramic membrane filter, gained concentrated solution is the concentrated solution of press lye; Concentrated 2-4 time of described nanofiltration membrane circulation, before each filtration, feed liquid all enters nanofiltration membrane after thin up;
B, extraction half fibre
By the concentrated solution acid neutralization of press lye, obtain half fine liquid;
C, enzymolysis
In half fine liquid, add prozyme, enzyme digestion reaction occurs and obtains enzymolysis solution;
D, purification
Enzymolysis solution is through ceramic membrane filter, and permeate enters nanofiltration membrane desalination, and gained concentrated solution is the refined solution of xylo-oligosaccharide, then obtains feed grade xylo-oligosaccharide through evaporation, oven dry.
2. according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described step A, ultra-filtration membrane molecular weight cut-off is 10000-15000, the molecular weight cut-off of described nanofiltration membrane is 200-400, and the molecular weight cut-off of ceramic membrane is 800-1500.
3. according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described step A, before each nanofiltration membrane, the amount of thin up is 1 times of stock liquid volume, filters the concentrated solution volume obtained identical with stock liquid volume.
4. according to claim 3 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described permeate is containing alkali 200-300g/l, containing half fine 40-80 g/l, after nanofiltration membrane circulation is concentrated, obtain concentrated solution containing alkali 12-75g/l, containing half fine 40-80g/l.
5. according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described step A, feed liquid first enters ceramic membrane device through thin up, add water to feed liquid gradation in working cycle, total amount of water is 5 times of material liquid volume, and gained concentrated solution volume is identical with stock liquid volume.
6. according to claim 5 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: containing alkali 2-4g/l in the concentrated solution of described ceramic membrane filter, containing half fine 40-80 g/l.
7. according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described step A, the temperature of ultrafiltration is 30-40 DEG C, and the temperature of nanofiltration membrane is 40-60 DEG C, and the temperature of ceramic membrane filter is 60-80 DEG C.
8. according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described step A, the mistake mould difference of ultrafiltration is 2-3bar, and the mistake mould difference of nanofiltration membrane is 3-4bar, and the mistake mould difference of ceramic membrane is 5-6bar.
9. according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described step A, feed liquid is 60-80m at the flow of ultra-filtration membrane 3/ h, the flow in nanofiltration membrane is 25-40m 3/ h, the flow in ceramic membrane is 200-250m 3/ h.
10. according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described step A, it is 26.8m that the list of ultra-filtration membrane props up filtration area 2, it is 26.8m that the list of nanofiltration membrane props up filtration area 2, it is 0.6m that the list of ceramic membrane props up filtration area 2.
11. is according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described step B, concentrated solution acid neutralization, refers to and add hydrochloric acid neutralization, make pH value be 4-5.
12. is according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, and it is characterized in that: described step C, prozyme is zytase, cellulase and polygalacturonase, and ratio is 3:2:1.
13. is according to claim 12 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: the enzymolysis time of described enzyme digestion reaction is 0.5-2h, and temperature is 50-60 DEG C, and the pH value of enzyme digestion reaction is 4-5.
14. is according to claim 12 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: the enzyme concentration of described enzyme digestion reaction is 0.5-1.5%.
15. is according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described D step, and the molecular weight cut-off of ceramic membrane is 800-1500.
16. is according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described D step, and the molecular weight cut-off of nanofiltration membrane is 100-200.
17. is according to claim 16 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: the mistake mould difference of described nanofiltration membrane is 3-4bar, and temperature is 30-40 DEG C, and single filtration area is 26.8 m 2.
18. is according to claim 1 with the technique of viscose fiber press lye for raw material production feed grade xylo-oligosaccharide, it is characterized in that: described D step, and the material liquid volume before nanofiltration membrane concentrates is 10-15 times of concentrated solution volume.
CN201410622263.6A 2014-11-07 2014-11-07 Process for producing feed-grade xylo-oligosaccharide from viscose fiber squeezed alkali liquor Withdrawn CN104357591A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105420313A (en) * 2015-12-15 2016-03-23 宜宾雅泰生物科技有限公司 Method for preparing feed-grade xylo-oligosaccharide through viscose squeezed alkali liquid
CN105420292A (en) * 2015-12-15 2016-03-23 宜宾雅泰生物科技有限公司 Method for preparing xylitol through viscose squeezed alkali liquid
CN106367449A (en) * 2016-08-26 2017-02-01 唐山三友集团兴达化纤有限公司 Method for preparing feed-grade xylooligosaccharide from waste liquid generated in a production process of viscose staple fibers

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999028490A1 (en) * 1997-11-26 1999-06-10 Novo Nordisk A/S A method of producing oligosaccharide syrups, a system for producing the same and oligosaccharide syrups
CN1556110A (en) * 2004-01-05 2004-12-22 江南大学 Production method of high purity oligoxylose
CN101484632A (en) * 2006-05-10 2009-07-15 连津格股份公司 Process for producing a pulp
CN102061323A (en) * 2010-11-10 2011-05-18 山东龙力生物科技股份有限公司 Comprehensive utilization process of wood cellulose
CN102277761A (en) * 2011-07-19 2011-12-14 中国制浆造纸研究院 Method for preparing oligosaccharide and paper pulp
CN102643935A (en) * 2012-04-11 2012-08-22 宜宾丝丽雅股份有限公司 Method for preparing xylose by using squeezed waste alkali in viscose fiber production process
WO2012155239A1 (en) * 2011-05-18 2012-11-22 Mascoma Canada Inc. Lignin removal after enzymatic treatment of lignocellulosic materials
CN103243138A (en) * 2013-05-09 2013-08-14 许昌学院 Method for preparing corncob xylooligosaccharide by a complex enzyme method
CN103789356A (en) * 2014-02-26 2014-05-14 中国制浆造纸研究院 Method for preparing ethanol and xylooligosaccharide feed additive
CN104099431A (en) * 2014-08-01 2014-10-15 沈阳新华环境工程有限公司 Method for extracting xylose from viscoce chemical fiber squeezed alkali liquor

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999028490A1 (en) * 1997-11-26 1999-06-10 Novo Nordisk A/S A method of producing oligosaccharide syrups, a system for producing the same and oligosaccharide syrups
CN1556110A (en) * 2004-01-05 2004-12-22 江南大学 Production method of high purity oligoxylose
CN101484632A (en) * 2006-05-10 2009-07-15 连津格股份公司 Process for producing a pulp
CN102061323A (en) * 2010-11-10 2011-05-18 山东龙力生物科技股份有限公司 Comprehensive utilization process of wood cellulose
WO2012155239A1 (en) * 2011-05-18 2012-11-22 Mascoma Canada Inc. Lignin removal after enzymatic treatment of lignocellulosic materials
CN102277761A (en) * 2011-07-19 2011-12-14 中国制浆造纸研究院 Method for preparing oligosaccharide and paper pulp
CN102643935A (en) * 2012-04-11 2012-08-22 宜宾丝丽雅股份有限公司 Method for preparing xylose by using squeezed waste alkali in viscose fiber production process
CN103243138A (en) * 2013-05-09 2013-08-14 许昌学院 Method for preparing corncob xylooligosaccharide by a complex enzyme method
CN103789356A (en) * 2014-02-26 2014-05-14 中国制浆造纸研究院 Method for preparing ethanol and xylooligosaccharide feed additive
CN104099431A (en) * 2014-08-01 2014-10-15 沈阳新华环境工程有限公司 Method for extracting xylose from viscoce chemical fiber squeezed alkali liquor

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
丁明玉等编著: "《现代分离方法与技术》", 31 August 2006 *
何亮亮: "复合酶解蔗渣木聚糖制备低聚木糖的研究", 《中国优秀硕士学位论文全文数据库 工程科技I辑》 *
高悦: "用于碱纤压榨液过滤的纳滤膜技术", 《人造纤维》 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105420313A (en) * 2015-12-15 2016-03-23 宜宾雅泰生物科技有限公司 Method for preparing feed-grade xylo-oligosaccharide through viscose squeezed alkali liquid
CN105420292A (en) * 2015-12-15 2016-03-23 宜宾雅泰生物科技有限公司 Method for preparing xylitol through viscose squeezed alkali liquid
CN106367449A (en) * 2016-08-26 2017-02-01 唐山三友集团兴达化纤有限公司 Method for preparing feed-grade xylooligosaccharide from waste liquid generated in a production process of viscose staple fibers

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