CN101974104A - Preparation method of chitosan - Google Patents
Preparation method of chitosan Download PDFInfo
- Publication number
- CN101974104A CN101974104A CN 201010536585 CN201010536585A CN101974104A CN 101974104 A CN101974104 A CN 101974104A CN 201010536585 CN201010536585 CN 201010536585 CN 201010536585 A CN201010536585 A CN 201010536585A CN 101974104 A CN101974104 A CN 101974104A
- Authority
- CN
- China
- Prior art keywords
- chitosan
- shrimp shell
- preparation
- sodium hydroxide
- chitin
- 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
Links
Images
Landscapes
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
一种壳聚糖的制备方法。提供一种高脱乙酰度、高分子量的壳聚糖的制备方法，包括以下步骤：首先准备原料，用酸处理除去钙盐，再用碱处理除去蛋白，然后除去虾红素得甲壳素，所得甲壳素脱乙酰即得壳聚糖。与现有技术相比，具有以下优点：除钙和除虾红素的时间缩短，提高了壳聚糖的分子量。使用碱间歇法分步脱乙酰，使制备获得的壳聚糖脱乙酰度达到91％～93％，粘均分子量为8.9×105～94×105。A preparation method of chitosan. A preparation method of chitosan with high degree of deacetylation and high molecular weight is provided, comprising the following steps: firstly preparing raw materials, treating with acid to remove calcium salt, then treating with alkali to remove protein, and then removing astaxanthin to obtain chitin, the obtained Chitosan is obtained by deacetylation of chitin. Compared with the prior art, it has the following advantages: the time for removing calcium and astaxanthin is shortened, and the molecular weight of chitosan is increased. The step-by-step deacetylation of the alkali batch method is used, so that the degree of deacetylation of the prepared chitosan reaches 91% to 93%, and the viscosity average molecular weight is 8.9×10 5 to 94×10 5 .
Description
Technical field
The present invention relates to the preparation method of polymer glycan, particularly a kind of preparation method of chitosan.
Background technology
Chitosan is a kind of important biomaterial, because its unique characteristic and function more and more get more and more people's extensive concerning.The main application fields of chitosan is medicine, food, environmental protection, agricultural etc., at present, both at home and abroad to the chitosan especially demand of high purity of shell glycan grow with each passing day (Jiang Tingda. chitin [M]. Beijing: Chemical Industry Press, 2003:341-648).The method of utilizing shrimp and crab shells to prepare chitosan mainly is a chemical method, and its technical process comprises the acidleach desalination, soda boiling deproteinated, oxidative decoloration, concentrated base deacetylation.But present technical process is difficult to obtain simultaneously high deacetylized, high-molecular weight chitosan.For addressing this problem, Luo Xin etc. (Luo Xin. Preparation of Chitosan process modification [J]. the West China pharmaceutical journal, 1999,14 (1): 13-17) preparation technology is improved, 2 acidleach decalcification salt and 2 deproteinated are hocketed, protein and calcium salt remove more complete, but also can cause the soda acid consumption to increase, and raise the cost.Xing Ji bravely wait (Xing Jiyong. chitosan flocculant optimum preparation condition and liquid waste disposal [J]. Liaoning chemical industry, 2004,33 (9): 507-508) adopt interrupter method to handle in taking off the acetyl process, find deacetylation 85%, relative molecular mass reaches 6.8 * 10
5The processing condition of preparation chitosan.
Summary of the invention
The object of the present invention is to provide preparation method high deacetylized, a kind of chitosan of high-molecular weight.
The present invention includes following steps:
1) shrimp shell pre-treatment: fresh prawn shell is rinsed well, and oven dry is pulverized, and sieves, and promptly gets the shrimp shell after sieving;
2) calcium salt is removed in acid treatment: the shrimp shell after will sieving soaks with excessive hydrochloric acid, filters, and collects the shrimp shell, cleans, and removes hydrochloric acid remaining in the shrimp shell, promptly gets the shrimp shell after the deliming;
3) alkaline purification removes Deproteinization: the shrimp shell after the deliming with excessive sodium hydroxide solution immersion, is cooled off, filter, collect the shrimp shell, clean, remove residue sodium hydroxide in the shrimp shell, promptly get except that the shrimp shell behind the albumen;
4) remove astacin: will soak in potassium permanganate solution except that the shrimp shell behind the albumen, filter, filtration product is soaked in sodium sulfite solution, filter, clean, drying promptly gets chitin;
5) acetyl is taken off in alkaline purification: chitin is soaked with excessive sodium hydroxide solution, and cooling is filtered, and the cleaning and filtering product is removed residue sodium hydroxide, and oven dry promptly gets chitosan.
In step 1), the described mesh size that sieves can be 100～150 μ m.
In step 2) in, the volume ratio of shrimp shell and hydrochloric acid can be 1 during described the immersion: (5～10), the mass concentration of described hydrochloric acid can be 5%～15%, and the time of described immersion can be 4～6h.
In step 3), the volume ratio of shrimp shell and sodium hydroxide solution can be 1 during described the immersion: (5～10), the mass concentration of described sodium hydroxide solution can be 10%～20%, and described immersion can be soaked 1～2h under 80～90 ℃ of temperature.
In step 4), the mass concentration of described potassium permanganate solution can be 2%～5%; The described time that will soak in potassium permanganate solution except that the shrimp shell behind the albumen can be 0.5～1h, and the mass concentration of described sodium sulfite solution can be 5%～10%, and the described time that filtration product is soaked in sodium sulfite solution can be 0.5～1h.
In step 5), the mass concentration of described sodium hydroxide solution can be 40%～45%, described chitin be can be with the condition that excessive sodium hydroxide solution soaks: temperature is 90～110 ℃, soaks each 2～4h 1～2 time; Before the described oven dry, can wash by water filtration product, remove residue sodium hydroxide, clean at least 1 time with dehydrated alcohol again.
The preparation method of a kind of chitosan of the present invention compared with prior art has the following advantages:
1) the shrimp shell after will pulverizing uses the screen cloth in 100～150 μ m apertures to sieve, and makes the time of deliming shorten, and can improve the molecular weight of product chitosan.
2) in removing the step of astacin, because potassium permanganate has strong oxidizing property, the energy degrade chitosan, therefore, the soak time that shortens potassium permanganate and sodium bisulfite can improve the molecular weight of chitosan.
3) in the step of taking off the acetyl step, use the alkali interrupter method to take off acetyl step by step, to influencing the experiment condition of deacetylating degree of chitosan, viscosity-average molecular weight, temperature of reaction (T), reaction times (t), naoh concentration (C
NaOH), study by orthogonal design, find that each factor to the influence of deacetylation is in proper order: t＞T＞C
NaOHInfluence to viscosity-average molecular weight is in proper order: C
NaOH＞T＞t takes all factors into consideration the processing condition that obtain optimum, makes the deacetylating degree of chitosan for preparing reach 91%～93%, and viscosity-average molecular weight is 8.9 * 10
5～94 * 10
5
Description of drawings
The infrared figure of the chitosan of Fig. 1 embodiment of the invention 5 preparations.In Fig. 1, X-coordinate is wave number (cm
-1), ordinate zou is the percentage transmitance, the carbonyl peak (1655cm of acid amides
-1) very weak, the N-H peak (1599cm of the amino of chitosan
-1) very strong, acid amides becomes amino behind the chitin deacetylase, and amino peak is strong, shows the deacetylating degree of chitosan height.
Fig. 2 is the x-ray diffraction pattern of the chitosan of the embodiment of the invention 5 preparations.In Fig. 2, X-coordinate be angle of diffraction 2 θ (°), ordinate zou is a diffraction peak intensity, chitosan locates to occur peak crystallization at 10.9 ° and 20.1 °, near the crystalline hydrate structure of the corresponding chitosan of the diffraction peak of angle of diffraction 2 θ 10.9 °, near the II shape crystalline texture of the corresponding chitosan of the diffraction peak 211 °.
Embodiment
Embodiment 1
1) prepare raw material: with fresh prawn shell clean dry, pulverizer is pulverized then, crosses the sub-sieve in 150 μ m apertures, promptly gets the shrimp shell after sieving;
2) calcium salt is removed in acid treatment: the shrimp shell after will sieving soaks 4h with excessive hydrochloric acid under agitation condition, filters, and collects the shrimp shell, and water thoroughly cleans, and removes hydrochloric acid remaining in the shrimp shell, promptly gets the shrimp shell after the deliming;
3) alkaline purification removes Deproteinization: the shrimp shell after the deliming is stirred under 90 ℃ of temperature with 10% excessive sodium hydroxide solution soak 2h, cooling is filtered, collection shrimp shell, and water thoroughly cleans, and removes residue sodium hydroxide in the shrimp shell, promptly gets except that the shrimp shell behind the albumen;
4) remove astacin: will in 2% potassium permanganate solution, under agitation condition, soak 0.5h except that the shrimp shell behind the albumen, filter, and wash with water to filtrate limpid till, this moment, filter residue was a purple, again filter residue is soaked 0.5 in 5% sodium sulfite solution under agitation condition, filter, water washes repeatedly guarantees that sodium bisulfite cleans up, 60 ℃ of dryings promptly get chitin;
5) take by weighing the dried chitin of 3g and pack in the there-necked flask, with 40%NaOH in 90 ℃ of reaction 1h, room temperature cooling, filter, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, reinstall in the there-necked flask, at 90 ℃ of reaction 1h, the room temperature cooling is filtered with 40%NaOH, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, wash twice with dehydrated alcohol again, the dry chitosan that gets.The gained deacetylating degree of chitosan is 85.38%, and viscosity-average molecular weight is 1.01 * 10
6
The measuring method of deacetylation: acid base titration
Get 3 parts of 0.3～0.5g chitosans, place the 250ml triangular flask, standard salt acid solution 30ml with 0.1mol/L, stir down at 20～25 ℃, dissolve (but adding distil water) therebetween fully until chitosan, add 6 indicator (tropeolin-D-aniline blue (volume ratio 1: 2)) then, become pale bluish green to solution with the free H+ of the standard caustic soda solution titration of 0.1mol/L.Other gets a duplicate samples, dries to constant weight at 105 ℃, measures 3 times, calculates water ratio (W).
Deacetylation (D.D.%)=203n/ (Q+42n)
N=C
1V
1-C
2V
2(C wherein
1, V
1Be respectively the concentration and the volume of hydrochloric acid, C
2, V
2Be respectively concentration sodium hydroxide and volume)
The Q=sample quality * (1-W).
Viscosity-average molecular weight adopts this area progressively dilution method commonly used to measure.
Embodiment 2
The preparation method of chitin is identical with embodiment 1, take by weighing the dried chitin of 3g and pack in the there-necked flask, with 40%NaOH at 100 ℃ of reaction 1.5h, the room temperature cooling is filtered, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, reinstall in the there-necked flask, react 1.5h at 100 ℃ with 40%NaOH, the room temperature cooling, filter, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, wash 2 times the dry chitosan that gets again with dehydrated alcohol.The gained deacetylating degree of chitosan is 89.19%, and viscosity-average molecular weight is 8.91 * 10
5
Embodiment 3
The preparation method of chitin is identical with embodiment 1, take by weighing the dried chitin of 3g and pack in the there-necked flask, with 40%NaOH at 110 ℃ of reaction 2h, the room temperature cooling is filtered, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, reinstall in the there-necked flask, react 2h at 110 ℃ with 40%NaOH, the room temperature cooling, filter, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, wash 2 times the dry chitosan that gets again with dehydrated alcohol.The gained deacetylating degree of chitosan is 95.2%, and viscosity-average molecular weight is 8.74 * 10
5
Embodiment 4
The preparation method of chitin is identical with embodiment 1, take by weighing the dried chitin of 3g and pack in the there-necked flask, with 45%NaOH at 90 ℃ of reaction 1.5h, the room temperature cooling is filtered, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, reinstall in the there-necked flask, react 1.5h at 90 ℃ with 45%NaOH, the room temperature cooling, filter, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, wash 2 times the dry chitosan that gets again with dehydrated alcohol.The gained deacetylating degree of chitosan is 88.76%, and viscosity-average molecular weight is 9.43 * 10
5
Embodiment 5
The preparation method of chitin is identical with embodiment 1, take by weighing the dried chitin of 3g and pack in the there-necked flask, with 45%NaOH at 100 ℃ of reaction 2h, the room temperature cooling is filtered, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, reinstall in the there-necked flask, react 2h at 100 ℃ with 45%NaOH, the room temperature cooling, filter, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, wash 2 times the dry chitosan that gets again with dehydrated alcohol.The gained deacetylating degree of chitosan is 93.62%, and viscosity-average molecular weight is 9.38 * 10
5
The infared spectrum of chitosan shows (referring to Fig. 1): the carbonyl peak (1655cm of acid amides
-1) very weak, the N-H peak (1599cm of the amino of chitosan
-1) very strong, acid amides becomes amino behind the chitin deacetylase, and amino peak is strong, the deacetylating degree of chitosan height.
The x-ray diffraction pattern of chitosan (referring to Fig. 2): chitosan locates to occur peak crystallization at 10.9 ° and 20.1 °, near the crystalline hydrate structure of the corresponding chitosan of the diffraction peak of angle of diffraction 2 θ 10.9 °, near the II shape crystalline texture of the corresponding chitosan of the diffraction peak 21.1 °.Bibliographical information (Samuels RJ.Solid state characterization of the structure of chitosan films[J] Polym.Sci.Polym.Phys.Ed, 1981,19 (7): 1081-1087), raising along with deacetylation, the I type structure of chitosan will change II type structure gradually into, and the order of structure improves.Illustrate that prepared chitosan of the present invention is mainly II type structure, and absorption peak is sharp-pointed, has good crystalline structure.
Embodiment 6
The preparation method of chitin is identical with embodiment 1, take by weighing the dried chitin of 3g and pack in the there-necked flask, with 45%NaOH at 110 ℃ of reaction 1h, the room temperature cooling is filtered, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, reinstall in the there-necked flask, in the cooling of 110 ℃ of reaction 1h room temperatures, filter with 45%NaOH, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, wash 2 times with dehydrated alcohol again, the dry chitosan that gets.The gained deacetylating degree of chitosan is 89.63%, and viscosity-average molecular weight is 9.07 * 10
5
Embodiment 7
The preparation method of chitin is identical with embodiment 1, take by weighing the dried chitin of 3g and pack in the there-necked flask, with 50%NaOH at 90 ℃ of reaction 2h, the room temperature cooling is filtered, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, reinstall in the there-necked flask, in the cooling of 90 ℃ of reaction 2h room temperatures, filter with 50%NaOH, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, wash 2 times with dehydrated alcohol again, the dry chitosan that gets.The gained deacetylating degree of chitosan is 90.29%, and viscosity-average molecular weight is 8.58 * 10
5
Embodiment 8
The preparation method of chitin is identical with embodiment 1, take by weighing the dried chitin of 3g and pack in the there-necked flask, with 50%NaOH at 100 ℃ of reaction 1h, the room temperature cooling is filtered, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, reinstall in the there-necked flask, in the cooling of 100 ℃ of reaction 1h room temperatures, filter with 50%NaOH, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, wash 2 times with dehydrated alcohol again, the dry chitosan that gets.The gained deacetylating degree of chitosan is 89.36%, and viscosity-average molecular weight is 8.92 * 10
5
Embodiment 9
The preparation method of chitin is identical with embodiment 1, take by weighing the dried chitin of 3g and pack in the there-necked flask, with 50%NaOH at 110 ℃ of reaction 1.5h, the room temperature cooling is filtered, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, reinstall in the there-necked flask, react 1.5h at 110 ℃ with 50%NaOH, the room temperature cooling, filter, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, wash 2 times the dry chitosan that gets again with dehydrated alcohol.The gained deacetylating degree of chitosan is 91.11%, and viscosity-average molecular weight is 74 * 10
5
Embodiment 10
The preparation method of chitin is identical with embodiment 1, take by weighing the dried chitin of 3g and pack in the there-necked flask, with 45%NaOH at 100 ℃ of reaction 4h, the room temperature cooling is filtered, and the thorough cleaning and filtering product of water, remove residue sodium hydroxide, wash 2 times, the dry chitosan that gets with dehydrated alcohol.The gained deacetylating degree of chitosan is about 80%, and viscosity-average molecular weight is 6.8 * 10
5
Claims (10)
1. the preparation method of a chitosan is characterized in that may further comprise the steps:
1) shrimp shell pre-treatment: fresh prawn shell is rinsed well, and oven dry is pulverized, and sieves, and promptly gets the shrimp shell after sieving;
2) calcium salt is removed in acid treatment: the shrimp shell after will sieving soaks with excessive hydrochloric acid, filters, and collects the shrimp shell, cleans, and removes hydrochloric acid remaining in the shrimp shell, promptly gets the shrimp shell after the deliming;
3) alkaline purification removes Deproteinization: the shrimp shell after the deliming with excessive sodium hydroxide solution immersion, is cooled off, filter, collect the shrimp shell, clean, remove residue sodium hydroxide in the shrimp shell, promptly get except that the shrimp shell behind the albumen;
4) remove astacin: will soak in potassium permanganate solution except that the shrimp shell behind the albumen, filter, filtration product is soaked in sodium sulfite solution, filter, clean, drying promptly gets chitin;
5) acetyl is taken off in alkaline purification: chitin is soaked with excessive sodium hydroxide solution, and cooling is filtered, and the cleaning and filtering product is removed residue sodium hydroxide, and oven dry promptly gets chitosan.
2. the preparation method of a kind of chitosan as claimed in claim 1 is characterized in that in step 1), and the described mesh size that sieves is 100～150 μ m.
3. the preparation method of a kind of chitosan as claimed in claim 1 is characterized in that in step 2) in, the volume ratio of shrimp shell and hydrochloric acid is 1: 5～10 during described the immersion.
4. the preparation method of a kind of chitosan as claimed in claim 1 is characterized in that in step 2) in, the mass concentration of described hydrochloric acid is 5%～15%, the time of described immersion is 4～6h.
5. the preparation method of a kind of chitosan as claimed in claim 1 is characterized in that in step 3), and the volume ratio of shrimp shell and sodium hydroxide solution is 1: 5～10 during described the immersion.
6. the preparation method of a kind of chitosan as claimed in claim 1 is characterized in that in step 3), and the mass concentration of described sodium hydroxide solution is 10%～20%, and described immersion is to soak 1～2h under 80～90 ℃ of temperature.
7. the preparation method of a kind of chitosan as claimed in claim 1 is characterized in that in step 4), and the mass concentration of described potassium permanganate solution is 2%～5%; The described time that will soak in potassium permanganate solution except that the shrimp shell behind the albumen is 0.5～1h.
8. the preparation method of a kind of chitosan as claimed in claim 1 is characterized in that in step 4), and the mass concentration of described sodium sulfite solution is 5%～10%, and the described time that filtration product is soaked in sodium sulfite solution is 0.5～1h.
9. the preparation method of a kind of chitosan as claimed in claim 1, it is characterized in that in step 5), the mass concentration of described sodium hydroxide solution is 40%～45%, describedly with chitin with the condition that excessive sodium hydroxide solution soaks be: temperature is 90～110 ℃, soak each 2～4h 1～2 time.
10. the preparation method of a kind of chitosan as claimed in claim 1 is characterized in that in step 5), before the described oven dry, is water cleaning and filtering product, removes residue sodium hydroxide, cleans at least 1 time with dehydrated alcohol again.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 201010536585 CN101974104A (en) | 2010-11-09 | 2010-11-09 | Preparation method of chitosan |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 201010536585 CN101974104A (en) | 2010-11-09 | 2010-11-09 | Preparation method of chitosan |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101974104A true CN101974104A (en) | 2011-02-16 |
Family
ID=43574019
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 201010536585 Pending CN101974104A (en) | 2010-11-09 | 2010-11-09 | Preparation method of chitosan |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN101974104A (en) |
Cited By (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102352568A (en) * | 2011-10-26 | 2012-02-15 | 芜湖南翔羽绒有限公司 | Arrangement method for down feathers with antibacterial function |
| CN102702389A (en) * | 2012-06-29 | 2012-10-03 | 中国人民解放军第二军医大学 | Thermo-sensitive chitosan derivative-hydroxypentyl chitosan and preparation method thereof |
| CN102808239A (en) * | 2012-08-24 | 2012-12-05 | 东北林业大学 | Method for preparing chitin nano filaments |
| CN103665191A (en) * | 2013-12-25 | 2014-03-26 | 嘉兴职业技术学院 | Preparation method of chitosan and immersion device for preparing chitosan |
| CN103665190A (en) * | 2013-12-11 | 2014-03-26 | 深圳先进技术研究院 | Method for preparing chitosan with ultrahigh deacetylation degree from euphausia superba as raw material |
| CN103689073A (en) * | 2013-12-16 | 2014-04-02 | 苏州安特实业有限公司 | Preparation technology of fruit and vegetable fresh-keeping agent |
| CN103690956A (en) * | 2013-12-31 | 2014-04-02 | 深圳先进技术研究院 | Hemostatic powder and preparation method thereof |
| CN103990437A (en) * | 2014-06-05 | 2014-08-20 | 江苏戚伍水产发展股份有限公司 | Method for preparing high-adsorptive property biological material by residue extracted by shrimp shell enzymic method |
| CN105399523A (en) * | 2015-12-12 | 2016-03-16 | 常州大学 | Method for preparing coated sustained-release calcium fertilizer from waste seafood shell |
| CN105750298A (en) * | 2016-02-29 | 2016-07-13 | 武汉大学 | Preparation method of shrimp shell powder |
| CN106167581A (en) * | 2016-08-17 | 2016-11-30 | 倪协照 | A kind of preparation method of antibacterial polypropylene |
| CN106280797A (en) * | 2016-08-17 | 2017-01-04 | 瑞安市智造科技有限公司 | A kind of antibiotic fungus-resisting paint |
| CN106336466A (en) * | 2016-08-17 | 2017-01-18 | 吴冰滢 | Slow-release antibacterial agent and preparation method thereof |
| CN106893005A (en) * | 2017-03-28 | 2017-06-27 | 周景天 | A kind of manufacture craft of soluble chitin |
| CN108250461A (en) * | 2017-12-29 | 2018-07-06 | 舟山出入境检验检疫局综合技术服务中心 | A kind of preparation method for the chitosan microball for being used to adsorb saxitoxin |
| CN108283283A (en) * | 2017-12-29 | 2018-07-17 | 舟山出入境检验检疫局综合技术服务中心 | A kind of method of electron beam irradiation and chitosan microball interaction degradation ciguatoxin |
| CN108586830A (en) * | 2017-12-15 | 2018-09-28 | 浙江海洋大学 | A kind of preparation method of chitosan-gelatin edible freshness-keeping thin coat |
| CN108587811A (en) * | 2018-05-07 | 2018-09-28 | 安徽索亚装饰材料有限公司 | A kind of production method of skin carving cuticle removers |
| CN108940373A (en) * | 2018-07-16 | 2018-12-07 | 广东石油化工学院 | Based on shrimp, the organic reaction catalyst of crab waste and the preparation method and application thereof |
| CN110229250A (en) * | 2019-07-09 | 2019-09-13 | 张大庆 | A method of utilizing soda acid " three de- methods " chitin extraction |
| CN110514615A (en) * | 2019-08-23 | 2019-11-29 | 大连工业大学 | A Calculation Method of Infrared Fitting Calculation of Chitosan Deacetylation Degree |
| CN110746520A (en) * | 2019-12-03 | 2020-02-04 | 扬州日兴生物科技股份有限公司 | Novel efficient preparation method for chitosan production |
| CN110862426A (en) * | 2019-12-09 | 2020-03-06 | 山东润德生物科技有限公司 | Method for preparing high-purity glucosamine sulfate |
| CN111264608A (en) * | 2020-03-20 | 2020-06-12 | 马艳华 | Spicy crab and preparation method thereof |
| CN111683973A (en) * | 2017-12-15 | 2020-09-18 | 昆虫公司 | Chitin and method for chemically obtaining chitin and/or chitosan |
| WO2021180078A1 (en) * | 2020-03-13 | 2021-09-16 | 山东美佳集团有限公司 | Method for preparing chitosan using snow crab shells |
| CN114437249A (en) * | 2022-02-21 | 2022-05-06 | 龙岩学院 | Method for extracting chitosan from shrimp and crab shells in one step |
| CN118085781A (en) * | 2024-03-15 | 2024-05-28 | 福建农林大学 | Low free formaldehyde amino resin adhesive modified by depolymerized shrimp and crab shells and preparation method thereof |
| CN118085781B (en) * | 2024-03-15 | 2025-04-08 | 福建农林大学 | A depolymerized shrimp and crab shell modified low free formaldehyde amino resin adhesive and preparation method thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1324619A (en) * | 2000-05-18 | 2001-12-05 | 湖北省葛店开发区畅响生物工程园有限公司 | Health capsule of pure active chitosan and animal fiber |
| WO2009117499A1 (en) * | 2008-03-19 | 2009-09-24 | Agratech International, Inc. | Chitosan manufacturing process |
-
2010
- 2010-11-09 CN CN 201010536585 patent/CN101974104A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1324619A (en) * | 2000-05-18 | 2001-12-05 | 湖北省葛店开发区畅响生物工程园有限公司 | Health capsule of pure active chitosan and animal fiber |
| WO2009117499A1 (en) * | 2008-03-19 | 2009-09-24 | Agratech International, Inc. | Chitosan manufacturing process |
Non-Patent Citations (1)
| Title |
|---|
| 《日用化学工业》 19980831 张延坤，刘国忠 甲壳素与壳聚糖及其衍生物的制备和在日化工业中的应用 36-40 1-10 , 第4期 2 * |
Cited By (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102352568B (en) * | 2011-10-26 | 2013-06-19 | 芜湖南翔羽绒有限公司 | Arrangement method for down feathers with antibacterial function |
| CN102352568A (en) * | 2011-10-26 | 2012-02-15 | 芜湖南翔羽绒有限公司 | Arrangement method for down feathers with antibacterial function |
| CN102702389A (en) * | 2012-06-29 | 2012-10-03 | 中国人民解放军第二军医大学 | Thermo-sensitive chitosan derivative-hydroxypentyl chitosan and preparation method thereof |
| CN102808239B (en) * | 2012-08-24 | 2014-04-02 | 东北林业大学 | Method for preparing chitin nano filaments |
| CN102808239A (en) * | 2012-08-24 | 2012-12-05 | 东北林业大学 | Method for preparing chitin nano filaments |
| CN103665190B (en) * | 2013-12-11 | 2016-01-20 | 深圳先进技术研究院 | A kind of take krill as the preparation method of the chitosan with ultrahigh deacetylation degree of raw material |
| CN103665190A (en) * | 2013-12-11 | 2014-03-26 | 深圳先进技术研究院 | Method for preparing chitosan with ultrahigh deacetylation degree from euphausia superba as raw material |
| CN103689073A (en) * | 2013-12-16 | 2014-04-02 | 苏州安特实业有限公司 | Preparation technology of fruit and vegetable fresh-keeping agent |
| CN103665191A (en) * | 2013-12-25 | 2014-03-26 | 嘉兴职业技术学院 | Preparation method of chitosan and immersion device for preparing chitosan |
| CN103665191B (en) * | 2013-12-25 | 2016-06-01 | 嘉兴职业技术学院 | The preparation method of a kind of chitosan and prepare the liquid-immersion device of chitosan |
| CN103690956A (en) * | 2013-12-31 | 2014-04-02 | 深圳先进技术研究院 | Hemostatic powder and preparation method thereof |
| CN103990437A (en) * | 2014-06-05 | 2014-08-20 | 江苏戚伍水产发展股份有限公司 | Method for preparing high-adsorptive property biological material by residue extracted by shrimp shell enzymic method |
| CN105399523A (en) * | 2015-12-12 | 2016-03-16 | 常州大学 | Method for preparing coated sustained-release calcium fertilizer from waste seafood shell |
| CN105750298A (en) * | 2016-02-29 | 2016-07-13 | 武汉大学 | Preparation method of shrimp shell powder |
| CN106167581A (en) * | 2016-08-17 | 2016-11-30 | 倪协照 | A kind of preparation method of antibacterial polypropylene |
| CN106280797A (en) * | 2016-08-17 | 2017-01-04 | 瑞安市智造科技有限公司 | A kind of antibiotic fungus-resisting paint |
| CN106336466A (en) * | 2016-08-17 | 2017-01-18 | 吴冰滢 | Slow-release antibacterial agent and preparation method thereof |
| CN106893005A (en) * | 2017-03-28 | 2017-06-27 | 周景天 | A kind of manufacture craft of soluble chitin |
| CN111683973A (en) * | 2017-12-15 | 2020-09-18 | 昆虫公司 | Chitin and method for chemically obtaining chitin and/or chitosan |
| CN111683973B (en) * | 2017-12-15 | 2023-08-29 | 昆虫公司 | Chitin and method for chemically obtaining chitin and/or chitosan |
| CN108586830A (en) * | 2017-12-15 | 2018-09-28 | 浙江海洋大学 | A kind of preparation method of chitosan-gelatin edible freshness-keeping thin coat |
| US11673973B2 (en) | 2017-12-15 | 2023-06-13 | Ynsect | Chitin and method for chemically obtaining chitin and/or chitosan |
| CN108250461A (en) * | 2017-12-29 | 2018-07-06 | 舟山出入境检验检疫局综合技术服务中心 | A kind of preparation method for the chitosan microball for being used to adsorb saxitoxin |
| CN108283283A (en) * | 2017-12-29 | 2018-07-17 | 舟山出入境检验检疫局综合技术服务中心 | A kind of method of electron beam irradiation and chitosan microball interaction degradation ciguatoxin |
| CN108587811A (en) * | 2018-05-07 | 2018-09-28 | 安徽索亚装饰材料有限公司 | A kind of production method of skin carving cuticle removers |
| CN108940373A (en) * | 2018-07-16 | 2018-12-07 | 广东石油化工学院 | Based on shrimp, the organic reaction catalyst of crab waste and the preparation method and application thereof |
| CN108940373B (en) * | 2018-07-16 | 2021-07-09 | 广东石油化工学院 | Organic reaction catalyst based on shrimp and crab waste and its preparation method and application |
| CN110229250A (en) * | 2019-07-09 | 2019-09-13 | 张大庆 | A method of utilizing soda acid " three de- methods " chitin extraction |
| CN110514615A (en) * | 2019-08-23 | 2019-11-29 | 大连工业大学 | A Calculation Method of Infrared Fitting Calculation of Chitosan Deacetylation Degree |
| CN110514615B (en) * | 2019-08-23 | 2021-09-10 | 大连工业大学 | Calculation method for calculating deacetylation degree of chitosan through infrared fitting |
| CN110746520A (en) * | 2019-12-03 | 2020-02-04 | 扬州日兴生物科技股份有限公司 | Novel efficient preparation method for chitosan production |
| CN110862426A (en) * | 2019-12-09 | 2020-03-06 | 山东润德生物科技有限公司 | Method for preparing high-purity glucosamine sulfate |
| WO2021180078A1 (en) * | 2020-03-13 | 2021-09-16 | 山东美佳集团有限公司 | Method for preparing chitosan using snow crab shells |
| CN111264608A (en) * | 2020-03-20 | 2020-06-12 | 马艳华 | Spicy crab and preparation method thereof |
| CN114437249A (en) * | 2022-02-21 | 2022-05-06 | 龙岩学院 | Method for extracting chitosan from shrimp and crab shells in one step |
| CN118085781A (en) * | 2024-03-15 | 2024-05-28 | 福建农林大学 | Low free formaldehyde amino resin adhesive modified by depolymerized shrimp and crab shells and preparation method thereof |
| CN118085781B (en) * | 2024-03-15 | 2025-04-08 | 福建农林大学 | A depolymerized shrimp and crab shell modified low free formaldehyde amino resin adhesive and preparation method thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101974104A (en) | Preparation method of chitosan | |
| CN102145280B (en) | Method for preparing rice hull active carbon/silicon dioxide/titanium dioxide composite material | |
| CN102964467B (en) | New process for preparing chitin | |
| CN101143905B (en) | A kind of green extraction method of agar | |
| CN102504327B (en) | Method for preparing cellulose sponge by utilizing sisal hemp wastes hemp bran and hemp head | |
| CN111560079A (en) | Preparation method of Iota carrageenan glue solution | |
| CN104761650A (en) | Preparation method of carrageenan | |
| CN105727895A (en) | Shaddock peel activated carbon-chitosan adsorbent and preparation method and application thereof | |
| JP2017504697A (en) | Cleaning product and preparation method thereof | |
| CN105542017B (en) | The preparation technology of sodium carboxymethylcellulose | |
| CN101703177A (en) | Method for removing sulfur dioxide in konjac flour | |
| CN1891719B (en) | A kind of preparation method of chitin and chitosan of tortoise foot shell | |
| JP7213347B2 (en) | Method for preparing chitosan using snow crab shell | |
| CN101445547A (en) | Method for preparing fishskin collagen with high molecular weight in a thermal-dissolving way at low temperature | |
| CN107522797B (en) | A kind of production technology of low-viscosity high water-holding agar | |
| CN101904413B (en) | Process for extracting proteins and dietary fibers by utilizing kelp residues | |
| CN102190816B (en) | Marine polysaccharide and manufacturing process thereof | |
| CN101928349B (en) | Application of a kind of electrogenerated functional water in the soaking process of corn starch production | |
| CN104341797A (en) | After-treatment clean process for purifying vat blue 66 dye | |
| CN113667028B (en) | Preparation method of Kappa carrageenan glue solution | |
| CN101845049B (en) | A process for removing lead from ellagic acid taking carboxymethyl starch as trapping agent | |
| CN116003644B (en) | Alkali extraction method for extracting kappa-carrageenan from red algae | |
| CN115109432A (en) | Method for converting indigo by rolling and breaking walls of indole alkaloids in malayan leaves | |
| CN112159483A (en) | Preparation method of Kappa carrageenan glue solution | |
| CN105199009B (en) | A kind of method for preparing high purity pectin using capsanthin glue discarded object |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C12 | Rejection of a patent application after its publication | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20110216 |