CN108424478A - A kind of inulin preparation method and preparation system - Google Patents
A kind of inulin preparation method and preparation system Download PDFInfo
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- CN108424478A CN108424478A CN201810376322.4A CN201810376322A CN108424478A CN 108424478 A CN108424478 A CN 108424478A CN 201810376322 A CN201810376322 A CN 201810376322A CN 108424478 A CN108424478 A CN 108424478A
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- resin
- inulin
- desalination
- concentration
- equipment
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- 229920001202 Inulin Polymers 0.000 title claims abstract description 63
- JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 title claims abstract description 62
- 229940029339 inulin Drugs 0.000 title claims abstract description 62
- 238000002360 preparation method Methods 0.000 title claims abstract description 29
- 239000011347 resin Substances 0.000 claims abstract description 73
- 229920005989 resin Polymers 0.000 claims abstract description 73
- 238000010612 desalination reaction Methods 0.000 claims abstract description 44
- 238000001728 nano-filtration Methods 0.000 claims abstract description 42
- 238000004061 bleaching Methods 0.000 claims abstract description 23
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000012535 impurity Substances 0.000 claims abstract description 11
- 238000005352 clarification Methods 0.000 claims abstract description 10
- 238000002386 leaching Methods 0.000 claims abstract description 7
- 239000002002 slurry Substances 0.000 claims abstract description 7
- 238000001694 spray drying Methods 0.000 claims abstract description 7
- 239000007788 liquid Substances 0.000 claims description 43
- 239000012528 membrane Substances 0.000 claims description 25
- 238000001223 reverse osmosis Methods 0.000 claims description 21
- 239000007787 solid Substances 0.000 claims description 20
- 150000001768 cations Chemical class 0.000 claims description 16
- 150000001450 anions Chemical class 0.000 claims description 14
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 10
- 150000002772 monosaccharides Chemical class 0.000 claims description 9
- 238000000605 extraction Methods 0.000 claims description 7
- 240000008892 Helianthus tuberosus Species 0.000 claims description 5
- 235000003230 Helianthus tuberosus Nutrition 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 238000005342 ion exchange Methods 0.000 claims description 4
- 244000298479 Cichorium intybus Species 0.000 claims description 3
- 235000007542 Cichorium intybus Nutrition 0.000 claims description 3
- 238000000909 electrodialysis Methods 0.000 claims description 3
- 239000003337 fertilizer Substances 0.000 claims description 3
- 238000005189 flocculation Methods 0.000 claims description 3
- 230000016615 flocculation Effects 0.000 claims description 3
- 230000002262 irrigation Effects 0.000 claims description 3
- 238000003973 irrigation Methods 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 239000002994 raw material Substances 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 239000002351 wastewater Substances 0.000 abstract description 2
- 239000011575 calcium Substances 0.000 description 15
- 150000003839 salts Chemical class 0.000 description 7
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 6
- 229910001424 calcium ion Inorganic materials 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000002585 base Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- NKWPZUCBCARRDP-UHFFFAOYSA-L calcium bicarbonate Chemical compound [Ca+2].OC([O-])=O.OC([O-])=O NKWPZUCBCARRDP-UHFFFAOYSA-L 0.000 description 3
- 229910000020 calcium bicarbonate Inorganic materials 0.000 description 3
- 239000000287 crude extract Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 244000035851 Chrysanthemum leucanthemum Species 0.000 description 2
- 235000008495 Chrysanthemum leucanthemum Nutrition 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- JXRVKYBCWUJJBP-UHFFFAOYSA-L calcium;hydrogen sulfate Chemical compound [Ca+2].OS([O-])(=O)=O.OS([O-])(=O)=O JXRVKYBCWUJJBP-UHFFFAOYSA-L 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 235000013325 dietary fiber Nutrition 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- BJHIKXHVCXFQLS-UYFOZJQFSA-N fructose group Chemical group OCC(=O)[C@@H](O)[C@H](O)[C@H](O)CO BJHIKXHVCXFQLS-UYFOZJQFSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 230000000968 intestinal effect Effects 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000008929 regeneration Effects 0.000 description 2
- 238000011069 regeneration method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- ZGXJTSGNIOSYLO-UHFFFAOYSA-N 88755TAZ87 Chemical compound NCC(=O)CCC(O)=O ZGXJTSGNIOSYLO-UHFFFAOYSA-N 0.000 description 1
- 241000186000 Bifidobacterium Species 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 235000000604 Chrysanthemum parthenium Nutrition 0.000 description 1
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 1
- RFSUNEUAIZKAJO-VRPWFDPXSA-N D-fructofuranose group Chemical group OCC1(O)[C@@H](O)[C@H](O)[C@H](O1)CO RFSUNEUAIZKAJO-VRPWFDPXSA-N 0.000 description 1
- 235000012040 Dahlia pinnata Nutrition 0.000 description 1
- 244000115658 Dahlia pinnata Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 235000003228 Lactuca sativa Nutrition 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- -1 albumen Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000000675 anti-caries Effects 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 206010012601 diabetes mellitus Diseases 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000008384 feverfew Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 231100000784 hepatotoxin Toxicity 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 229940118199 levulan Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0051—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Fructofuranans, e.g. beta-2,6-D-fructofuranan, i.e. levan; Derivatives thereof
- C08B37/0054—Inulin, i.e. beta-2,1-D-fructofuranan; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0003—General processes for their isolation or fractionation, e.g. purification or extraction from biomass
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Sustainable Development (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Water Treatment By Sorption (AREA)
Abstract
The invention discloses a kind of inulin preparation methods, which is characterized in that inulin leaching liquor or inulin slurries are through Ca (OH)2‑CO2Or Ca (OH)2‑SO2Inulin product is obtained after carrying out resin softening, nanofiltration concentration, desalination and de- monosaccharide, resin desalination bleaching, concentration, spray drying after removal of impurities clarification, activated carbon decolorizing.The invention also discloses a kind of inulin preparation systems.Inulin preparation method of the present invention and preparation system, using resin softening, nanofiltration concentration, desalination and de- monosaccharide, resin desalination, concentration technology, equipment and operating cost can be effectively reduced, equipment scaling, moisture usage amount and subsequent waste water yield are reduced.
Description
Technical field
The present invention relates to inulin to run field, more particularly to a kind of inulin preparation method and preparation system.
Background technology
Inulin (inulins) is also known as synanthrin, is distributed widely in nature, is the carbohydrate of a kind of natural levulan,
Characteristic with oligofructose and dietary fiber, in stem tuber and the chrysanthemum of feverfew such as witloof, jerusalem artichoke, dahlia and wild chrysanthemum
Exist with colloidal state in lettuce root system, structure is by dehydration by D- fructofuranoses residue (F) with β-(2-1)-glucosides
On the straight chain fructose side-chain structure that key polymerization is formed by connecting, end can be connected with glucose residue (G).It is different according to fructose side chain,
The degree of polymerization of inulin is between 2-60, average degree of polymerization 30.
The physiologic function of inulin mainly has:The balance of blood glucose, blood fat is adjusted, Cycle of nutrients and metabolism are improved;Subtract
Few hepatotoxin, toxin-expelling and face nourishing also have preventive and therapeutic action to cancer;Intestinal bifidobacteria proliferation is irritated, inhibits harmful micro-
The growth of biology, maintains the balance of intestinal flora;As a kind of soluble dietary fiber, anti-caries can promote mineral ion
Absorption and utilization, enhance the immunity function of human body, heat is low, and energy is high, is suitable for diabetic population.Due to inulin safety,
It is nontoxic, significantly improve body physiological function, be largely used to food, medicine and chemical industry.
China starts from the research of inulin in the 1990s, traditional operation process is first by raw material chopping, extraction
The inulin crude extract containing impurity such as albumen, pigment and mineral salts is obtained, Ca (OH) is then used2-CO2Or Ca (OH)2-SO2It is right
Inulin crude extract carries out removal of impurities clarification, then passes sequentially through strong acid, strong alkali ion exchange resin to remove the pigment and mine in solution
The impurity such as substance salt, finally spray drying obtain inulin product.The method is easy to operate, and cost is relatively low, but using Ca
(OH)2-CO2Or Ca (OH)2-SO2When carrying out removal of impurities clarification to inulin crude extract, a large amount of calcium bicarbonate or hydrogen sulfate will produce
Calcium, calcium bicarbonate or calcium bisulfate are soluble easily in water, bring great pressure to subsequent resin desalination and concentration, equipment is caused to be thrown
It provides of high cost, and needs in follow-up resin desalination to use a large amount of moisture, and then produce a large amount of desalinization wastewater, carry significantly
High environmental protection pressure, reduces the economic benefit of product.
Invention content
In view of the above-mentioned problems, the purpose of the present invention is to provide one kind can significantly reducing equipment investment cost, fortune is reduced
The inulin preparation method and preparation system of row cost.
In order to achieve the above objectives, technical solution proposed by the invention is:A kind of inulin preparation method, which is characterized in that
Inulin leaching liquor or inulin slurries are through Ca (OH)2-CO2Or Ca (OH)2-SO2It is soft that resin is carried out after removal of impurities clarification and activated carbon decolorizing
Change, nanofiltration concentration, desalination and de- monosaccharide, resin desalination bleaching, concentration obtains inulin product after spray drying.
Further, it is raw material that the inulin leaching liquor or inulin slurries, which are by jerusalem artichoke or witloof, successively by de-
After skin, chopping, as obtained by extraction or defibrination.
Further, the nanofiltration retaining molecular weight that the nanofiltration concentration, desalination and de- monosaccharide use is the road 150-300
Er Dun.
Further, the nanofiltration concentration, desalination and de- monosaccharide are that feed liquid is concentrated to solid content to be increased to 25-
When 30%, conductivity 3000-5000us/cm, into resin desalination bleaching.
Further, the resin desalination bleaching includes using resin cation, resin anion (R.A.), cation tree successively
The step of fat, resin anion (R.A.), resin cation, resin anion (R.A.) processing.
Further, the resin cation includes that strong acid type cationic resin, weak-type resin cation, macropore are strong
It is one or more in acid type resin cation or macropore weak-type resin cation;The resin anion (R.A.) includes strong base
One in resin anion (R.A.), weak base type resin anion (R.A.), macroporous strong-base type resin cation or macropore weak base type resin anion (R.A.)
Kind is a variety of.
Further, the concentration is concentrated using reverse osmosis or nanofiltration;The NF membrane group that the nanofiltration concentration uses
Part is preferably the high pressure resistant organic nanofiltration membrane component of pressure resistance ranging from 0-90bar, and molecular cut off is 150-300 dalton, or
The reverse osmosis membrane assembly that the reverse osmosis concentration uses is high pressure resistant organic reverse osmosis membrane group of pressure resistance ranging from 0-90bar
Part.
Further, the concentration is to stop concentrating when solid content in feed liquid is concentrated to 45% or more, is sprayed
It is dry.
Further, the resin regeneration solution after the resin desalination bleaching uses sulfuric acid and potassium hydroxide;Further include
Regenerated liquid electrodialysis or film are concentrated to 15% or more mass concentration, field irrigation is returned directly to as liquid fertilizer
Step.
The invention also includes a kind of inulin preparation systems, which is characterized in that including clear with the sequentially connected flocculation of material liquid tank
Clear equipment, activated carbon decolorizing equipment, resin softening equipment, nanofiltration concentration, desalination and de- monosaccharide equipment;The described nanofiltration concentration,
The concentrated solution outlet of desalination and de- monosaccharide equipment is sequentially connected resin desalination bleaching equipment and concentrator, the concentrator
Concentrated solution outlet connect spray drying device.
Further, the nanofiltration retaining molecular weight that the nanofiltration concentration, desalination and de- monosaccharide use is the road 150-300
Er Dun.
Further, the resin softening equipment uses continuous ion exchange apparatus.
Further, the resin desalination bleaching equipment uses continuous ion exchange apparatus.
Further, the concentrator is reverse osmosis concentration equipment or nanofiltration concentrator;The nanofiltration concentration
The nanofiltration membrane component that equipment uses is preferably the high pressure resistant organic nanofiltration membrane component of pressure resistance ranging from 0-90bar, molecular cut off
The reverse osmosis membrane assembly used for 150-300 dalton or the reverse osmosis concentration equipment is pressure resistance ranging from 0-90bar's
High pressure resistant organic reverse osmosis membrane assembly.
Using above-mentioned technical proposal, inulin preparation method of the present invention and preparation system, have the advantage that for:
1) feed liquid softens after decoloration by resin, can effectively prevent the scale problems of follow-up equipment;
2) feed liquid carries out nanofiltration concentration, desalination and de- monosaccharide and first removes part monosaccharide and monovalent salt, subtract after resin softens
Salt and contents of monosaccharides in few inulin, while inulin concentration is improved, subsequent ion can be reduced in this way exchanges required equipment scale
60% or more;
3) the when continuous ionic exchange process that resin desalination bleaching preferably uses, can save the sulfuric acid and hydrogen of 35-50%
Aoxidize potassium application rate;Save 70% or so pure water consumption.Greatly increase 50% or more product design, it is possible to reduce subsequent concentration at
This;
4) feed liquid concentrator uses high power nanofiltration instead by original evaporation and concentration or reverse osmosis membrane concentrates, it is possible to reduce 30%
The equipment cost of left and right reduces by 50% or more operating cost.
Description of the drawings
Fig. 1 is inulin preparation system schematic diagram of the present invention.
Specific implementation mode
In the following with reference to the drawings and specific embodiments, the present invention will be further described.
The applicant is had found by studying existing preparation of industrialization inulin technique due to using Ca (OH)2-CO2Or Ca
(OH)2-SO2, the calcium bicarbonate or calcium bisulfate that will produce, and then hard water is generated, cause subsequent concentrator to generate fouling existing
As.Feed liquid after decoloration is first carried out resin softening by applicant, and then nanofiltration is filtered, and realizes the initial concentration of feed liquid, is led to simultaneously
It crosses nanofiltration and realizes removing monovalent salt, removing monosaccharide and part divalent salts, improve the feed concentration for carrying out resin desalination bleaching
And salt content and contents of monosaccharides, 60% or more of resin equipment scale can be significantly improved, while resin desalination bleaching uses
Continuous ion exchange apparatus can substantially reduce inulin degradation probability, while the degradation using resin desalination bleaching than fixed bed
Rate few 70% can save the sulfuric acid and potassium hydroxide dosage of 35-50%;Save 70% or so pure water consumption.Greatly increase production
50% or more product concentration, it is possible to reduce subsequent concentration cost;Finally it is that concentration concentrates film using high power, it is possible to reduce 30% is left
Right equipment cost reduces by 50% or more operating cost.
As shown in Figure 1, inulin preparation system of the present invention, including set with 101 sequentially connected flocculation of material liquid tank clarification
Standby 102, activated carbon decolorizing equipment 103, resin softening equipment 104, nanofiltration concentration, desalination and de- monosaccharide equipment 105;Described receives
The concentrated solution outlet of filter concentration, desalination and de- monosaccharide equipment 105 is sequentially connected resin desalination bleaching equipment 106 and concentrator
107, the concentrated solution outlet of the concentrator 107 connects spray drying device 108.
Further, the nanofiltration retaining molecular weight that the nanofiltration concentration, desalination and de- monosaccharide equipment 105 use for
150-300 dalton;Preferably, the resin desalination bleaching equipment 107 and resin softening equipment 104 are handed over using continuous ionic
Exchange device;The concentrator 107 is reverse osmosis concentration equipment or nanofiltration concentrator;The nanofiltration concentrator uses
Nanofiltration membrane component be preferably pressure resistance ranging from 0-90bar high pressure resistant organic nanofiltration membrane component, molecular cut off 150-300
The reverse osmosis membrane assembly that dalton or the reverse osmosis concentration equipment use has for pressure-resistant the high pressure resistant of ranging from 0-90bar
Machine reverse osmosis membrane assembly.
Embodiment 1
Jerusalem artichoke leaching liquor is taken, through Ca (OH)2-CO2After removal of impurities clarification and activated carbon decolorizing, solid content exists in feed liquid
10%, calcium ion content 1000ppm, conductivity 7000us/cm;Conductivity is 10000us/ after feed liquid is softened by resin
Cm, calcium ion content 50ppm;Molecular cut off is used to be concentrated for the nanofiltration membrane of 150 dalton the feed liquid after softening
And after adding water elution, solid content is increased to 24% in feed liquid, and conductance is reduced to 4000us/cm, and contents of monosaccharides is reduced to 5% or less
When, it carries out continuous ionic and exchanges desalination bleaching, when conductance being further reduced to 100us/cm or less, feed liquid solid concentration exists
23%;It is concentrated again with high pressure resistant organic reverse osmosis membrane assembly of pressure resistance ranging from 0-90bar, the solid content in feed liquid is dense
After being reduced to 47%, be spray-dried to obtain inulin product, inulin concentration 96.3% in the inulin obtained after measured is less than containing ash content
0.2%, extraction yield reaches 98.8%.
Preferably, the resin regeneration solution after resin desalination bleaching can also be used sulfuric acid and potassium hydroxide;Further include
Regenerated liquid electrodialysis or film are concentrated to 15% or more mass concentration, field irrigation is returned directly to as liquid fertilizer
Step.
Embodiment 2
Jerusalem artichoke leaching liquor is taken, through Ca (OH)2-CO2After removal of impurities clarification and activated carbon decolorizing, solid content exists in feed liquid
10%, calcium ion content 800ppm, conductivity 7000us/cm;Conductivity is 8000us/ after feed liquid is softened by resin
Cm, calcium ion content 35ppm;Molecular cut off is used to be concentrated for the nanofiltration membrane of 300 dalton the feed liquid after softening
And after adding water elution, solid content is increased to 24% in feed liquid, and conductance is reduced to 3500us/cm, and contents of monosaccharides is reduced to 5% or less
When, it carries out continuous ionic and exchanges desalination bleaching, when conductance being further reduced to 100us/cm or less, feed liquid solid concentration exists
23%;It is concentrated again with high pressure resistant organic reverse osmosis membrane assembly of pressure resistance ranging from 0-90bar, the solid content in feed liquid is dense
After being reduced to 45%, be spray-dried to obtain inulin product, inulin concentration 97.3% in the inulin obtained after measured is less than containing ash content
0.2%, extraction yield reaches 98.8%.
Embodiment 3
Inulin slurries are taken, through Ca (OH)2-SO2After removal of impurities clarification and activated carbon decolorizing, in feed liquid solid content 10%,
Calcium ion content is 600ppm, conductivity 4000us/cm;After feed liquid is softened by resin conductivity be 7000us/cm, calcium from
Sub- content is 28ppm;It uses molecular cut off to be concentrated for the nanofiltration membrane of 200 dalton the feed liquid after softening and adds washing
After de-, solid content is increased to 24% in feed liquid, and conductance is reduced to 3600us/cm, when contents of monosaccharides is reduced to 5% or less, carries out
Continuous ionic exchanges desalination bleaching, and when conductance being further reduced to 100us/cm or less, feed liquid solid concentration is 23%;Again
It is concentrated with high pressure resistant organic reverse osmosis membrane assembly of pressure resistance ranging from 0-90bar, the solid content in feed liquid is concentrated to
After 46%, be spray-dried to obtain inulin product, inulin concentration 96.9% in the inulin obtained after measured is less than containing ash content
0.2%, extraction yield reaches 98.7%.
Embodiment 4
Inulin slurries are taken, through Ca (OH)2-SO2After removal of impurities clarification and activated carbon decolorizing, in feed liquid solid content 10%,
Calcium ion content is 500ppm, conductivity 6000us/cm;After feed liquid is softened by resin conductivity be 9000us/cm, calcium from
Sub- content is 32ppm;It uses molecular cut off to be concentrated for the nanofiltration membrane of 250 dalton the feed liquid after softening and adds washing
After de-, solid content is increased to 24% in feed liquid, and conductance is reduced to 4100us/cm, when contents of monosaccharides is reduced to 5% or less, carries out
Continuous ionic exchanges desalination bleaching, and when conductance being further reduced to 100us/cm or less, feed liquid solid concentration is 23%;Again
It is concentrated with high pressure resistant organic reverse osmosis membrane assembly of pressure resistance ranging from 0-90bar, the solid content in feed liquid is concentrated to
After 48%, be spray-dried to obtain inulin product, inulin concentration 96.6% in the inulin obtained after measured is less than containing ash content
0.2%, extraction yield reaches 98.6%.
Although specifically showing and describing the present invention in conjunction with preferred embodiment, those skilled in the art should be bright
In vain, it is not departing from the spirit and scope of the present invention defined by the appended claims, in the form and details to this hair
It is bright to make a variety of changes, it is protection scope of the present invention.
Claims (10)
1. a kind of inulin preparation method, which is characterized in that inulin leaching liquor or inulin slurries are through Ca (OH)2-CO2Or Ca (OH)2-
SO2Progress resin softening, nanofiltration concentration, desalination and de- monosaccharide, resin desalination bleaching are dense after removal of impurities clarification and activated carbon decolorizing
Contracting obtains inulin product after spray drying.
2. a kind of inulin preparation method according to claim 1, which is characterized in that the inulin leaching liquor or inulin slurry
It is raw material that liquid, which is by jerusalem artichoke or witloof, successively after decortication, chopping, as obtained by extraction or defibrination.
3. a kind of inulin preparation method according to claim 1, which is characterized in that the nanofiltration concentration, desalination and de-
Monosaccharide is that feed liquid is concentrated to solid content to be increased to 25-30%, de- into resin desalination when conductivity 3000-5000us/cm
Color.
4. a kind of inulin preparation method according to claim 1, which is characterized in that the resin desalination bleaching include according to
It is secondary to be handled using resin cation, resin anion (R.A.), resin cation, resin anion (R.A.), resin cation, resin anion (R.A.)
Step;The resin cation includes strong acid type cationic resin, weak-type resin cation, large porous strong acid cation tree
It is one or more in fat or macropore weak-type resin cation;The resin anion (R.A.) include strong base anion resin,
It is one or more in weak base type resin anion (R.A.), macroporous strong-base type resin cation or macropore weak base type resin anion (R.A.).
5. a kind of inulin preparation method according to claim 1, which is characterized in that the concentration is by solid in feed liquid
Object stops concentration when being concentrated to 45% or more, is spray-dried.
6. a kind of inulin preparation method according to claim 1, which is characterized in that the tree after the resin desalination bleaching
Fat actified solution uses sulfuric acid and potassium hydroxide;It further include the quality that regenerated liquid electrodialysis or film are concentrated to 15% or more
Concentration, the step of being returned directly to field irrigation as liquid fertilizer.
7. a kind of inulin preparation system, which is characterized in that including de- with the sequentially connected flocculation clarifying equipment of material liquid tank, activated carbon
Color equipment, resin softening equipment, nanofiltration concentration, desalination and de- monosaccharide equipment;Nanofiltration concentration, desalination and the de- monosaccharide equipment
Concentrated solution outlet be sequentially connected resin desalination bleaching equipment and concentrator, the concentrated solution outlet connection of the concentrator
Spray drying device.
8. a kind of inulin preparation system according to claim 7, which is characterized in that the nanofiltration concentration, desalination and de-
The nanofiltration retaining molecular weight that monosaccharide equipment uses is 150-300 dalton.
9. a kind of inulin preparation system according to claim 7, which is characterized in that the resin softening equipment or resin
Desalination bleaching equipment uses continuous ion exchange apparatus.
10. a kind of inulin preparation system according to claim 7, which is characterized in that the concentrator is reverse osmosis
Concentrator or nanofiltration concentrator;The nanofiltration membrane component that the nanofiltration concentrator uses is pressure resistance ranging from 0-90bar
High pressure resistant organic nanofiltration membrane component, molecular cut off is what 150-300 dalton or the reverse osmosis concentration equipment used
Reverse osmosis membrane assembly is high pressure resistant organic reverse osmosis membrane assembly of pressure resistance ranging from 0-90bar.
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101518307A (en) * | 2009-03-26 | 2009-09-02 | 山西益生元生物科技有限责任公司 | Method of extracting high-purity inulin from jerusalem artichoke and chicory |
CN101955553A (en) * | 2010-10-08 | 2011-01-26 | 九环菊芋生物产业股份有限公司 | Method for producing high-purity inulin |
CN202570191U (en) * | 2012-05-18 | 2012-12-05 | 丰宁平安高科实业有限公司 | Continuous ion exchange system for extracting inulin |
CN102898548A (en) * | 2012-09-19 | 2013-01-30 | 中国科学院烟台海岸带研究所 | Method for preparing inulin |
CN208949170U (en) * | 2018-04-25 | 2019-06-07 | 厦门欣赛科技有限公司 | A kind of inulin preparation system |
-
2018
- 2018-04-25 CN CN201810376322.4A patent/CN108424478A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101518307A (en) * | 2009-03-26 | 2009-09-02 | 山西益生元生物科技有限责任公司 | Method of extracting high-purity inulin from jerusalem artichoke and chicory |
CN101955553A (en) * | 2010-10-08 | 2011-01-26 | 九环菊芋生物产业股份有限公司 | Method for producing high-purity inulin |
CN202570191U (en) * | 2012-05-18 | 2012-12-05 | 丰宁平安高科实业有限公司 | Continuous ion exchange system for extracting inulin |
CN102898548A (en) * | 2012-09-19 | 2013-01-30 | 中国科学院烟台海岸带研究所 | Method for preparing inulin |
CN208949170U (en) * | 2018-04-25 | 2019-06-07 | 厦门欣赛科技有限公司 | A kind of inulin preparation system |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020182714A1 (en) | 2019-03-08 | 2020-09-17 | Sensus B.V. | Inulin composition and method of purifying inulin |
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