CN102286108A - Method for preparing potassium carboxymethylcellulose - Google Patents

Method for preparing potassium carboxymethylcellulose Download PDF

Info

Publication number
CN102286108A
CN102286108A CN2011101943841A CN201110194384A CN102286108A CN 102286108 A CN102286108 A CN 102286108A CN 2011101943841 A CN2011101943841 A CN 2011101943841A CN 201110194384 A CN201110194384 A CN 201110194384A CN 102286108 A CN102286108 A CN 102286108A
Authority
CN
China
Prior art keywords
potassium hydroxide
potassium
reaction
carboxymethyl cellulose
purified cotton
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN2011101943841A
Other languages
Chinese (zh)
Other versions
CN102286108B (en
Inventor
李友琦
邵自强
郭鸿雁
陈洋溢
王飞俊
王文俊
陈静
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beijing Institute of Technology BIT
Chongqing Lihong Fine Chemicals Co Ltd
Original Assignee
Beijing Institute of Technology BIT
Chongqing Lihong Fine Chemicals Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beijing Institute of Technology BIT, Chongqing Lihong Fine Chemicals Co Ltd filed Critical Beijing Institute of Technology BIT
Priority to CN2011101943841A priority Critical patent/CN102286108B/en
Publication of CN102286108A publication Critical patent/CN102286108A/en
Application granted granted Critical
Publication of CN102286108B publication Critical patent/CN102286108B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Polysaccharides And Polysaccharide Derivatives (AREA)

Abstract

The invention provides a method for producing potassium carboxymethylcellulose by a kneading method, which comprises the following steps of: alkalizing cellulose by high-concentration potassium hydroxide liquid and industrial potassium hydroxide solid to generate alkali cellulose; after the generated alkali cellulose is subjected to carboxymethylation of chloroacetic acid, adding the potassium hydroxide liquid and the industrial potassium hydroxide solid again to carry out secondary alkalization; then adding chloroacetic acid to carry out secondary carboxymethylation treatment; and washing, neutralizing, centrifuging, drying and grinding to obtain the potassium carboxymethylcellulose product. The product not only has good dissolubility, but also has simple production process, short reaction period, low equipment investment and low raw material consumption.

Description

A kind of preparation method of carboxymethyl cellulose potassium
Technical field
The present invention relates to a kind of preparation method of carboxymethyl cellulose potassium, belong to natural macromolecular material chemical modification field.
Technical background
Carboxymethyl cellulose potassium is that purified cotton and potassium hydroxide, Mono Chloro Acetic Acid alkalize under alkaline condition, etherification reaction and the water miscible fiber derivative that makes.In foodstuffs industry, CMC-Na uses as foodstuff additive commonly used, yet the excessive absorption of discovering sodium ion can cause diseases such as diabetes, hypertension, cardiovascular diseases, so will reduce the amount of sodium in daily life, can also replace sodium salt with part sylvite simultaneously; In petroleum industry, down hole problems such as well slough, bit freezing appear in regular meeting in the water-based drilling process, this is because when getting into mud shale stratum mostly, the hydration swelling of clay with disperse to be caused.Therefore, adopt chemical agent control drilling fluid medium to enter the stratum, the inhibition shale hydration expands and disperses, and is a kind of stabilizing borehole, the important means that guarantees normal drilling well, studies show that in inhibitor uses the effect suppressing the ground hydration swelling of CMC-K will be significantly better than CMC-Na.
Domestic less to CMC-K research at present, from document " the Different Alkali metal hydroxides is to the influence of a carboxymethyl celluloseization " literary composition, sum up and drawn some about CMC-Na and the correlated related conclusions of CMC-K, specific as follows:
(1) the NaOH massfraction is 25%, and Mierocrystalline cellulose reaches maximum swollen, is below or above this massfraction, and cellulosic moisture expansivity reduces; The KOH massfraction is 20% to 35%, and platform appears in cellulosic moisture expansivity, is lower than 20% or be higher than 35%, and the Mierocrystalline cellulose moisture expansivity increases with the increase of KOH massfraction.
(2) under the equal in quality mark, the absorption alkali number of Mierocrystalline cellulose in NaOH is higher than the adsorptive capacity in KOH.
(3) along with the increase of alkali number, the substitution value of product increases gradually, but the substitution value of CMC-Na increases rapidly, and the trend that the CMC-K substitution value increases is more slow.Within the specific limits, the consumption of alkali is big more, and Mierocrystalline cellulose is big more to the adsorptive capacity of alkali, the Mierocrystalline cellulose swollen is just good more, and cellulosic degree of crystallinity descends, thereby has improved the reactive behavior of hydroxyl on the unit loop, help the diffusion of etherifying agent, the utilization ratio of etherifying agent improves, and substitution value is also high more.In addition, because Na +Compare K +Reactive behavior higher, the former is better to cellulosic swollen, in etherification reaction, the utilization ratio of etherifying agent is much higher relatively, thereby causes the intensity of variation of same alkali number, the former sharply increases by substitution value, and the trend that the latter increases is more slow.
Because above factors have caused the substitution value of the carboxymethyl cellulose potassium produced under equal processing condition will be far below Xylo-Mucine.
The chemical reaction of preparation carboxymethyl cellulose potassium mainly contains two kinds at present: a kind of is that Mierocrystalline cellulose and potassium hydroxide base solution reaction generate soda cellulose; Soda cellulose carries out etherification reaction with Mono Chloro Acetic Acid again.Because this method substitution value is lower, so few people adopt the preparation of this kind method.Another kind is earlier CMC to be carried out acidifying, allows H +Replace the Na among the CMC +, and then, making carboxymethyl cellulose potassium with material after the acidifying and KOH liquid reactions, this method adopts many.Both compare, and the latter's operation will bother manyly than the former, and cost also will be higher than the former far away, but advantage is that the product substitution value that obtains is higher.
Summary of the invention
The present invention just is based on above background, obtains a kind of method that has than the carboxymethyl cellulose potassium of high substitution value by process modification.
Technical scheme of the present invention is as follows:
A kind of preparation method of carboxymethyl cellulose potassium may further comprise the steps:
A, with purified cotton and potassium hydroxide aqueous solution and the potassium hydroxide solid pulverized, drop into together with aqueous ethanolic solution and to carry out a quaternization in the kneader;
After b, alkalization finish, carry out etherification reaction, in 40 minutes, equably etherifying agent is sprayed in the material to the kneader, carry out etherification reaction one time;
E, last material obtain carboxymethyl cellulose potassium after pulverizing through washing.
After step b, further carry out following two steps, and then carry out step e, through after once alkalization and the etherificate, carry out double alkalisation and secondary etherificate more like this, mainly be to allow react more abundant, it is higher to work it out the product substitution value.
After c, etherification reaction finish,, drop in the material in the kneader together with aqueous ethanolic solution and to carry out the double alkalisation reaction once more with potassium hydroxide aqueous solution and potassium hydroxide solid;
Add etherifying agent once more after d, the double alkalisation reaction, carry out the secondary etherification reaction;
The mass percent concentration of described potassium hydroxide aqueous solution is 40~55%, is reaction medium with the aqueous ethanolic solution, and the mass percentage concentration of aqueous ethanolic solution is 70~98%; Described etherifying agent is chloroacetic ethanolic soln, and its mass percent concentration is 50~80%.
Wherein, a quaternization time is 50~80 minutes among the step a, and one time the quaternization temperature is 10~40 ℃.
An etherification reaction temperature is 80 ℃ ± 2 ℃ among the step a, and an etherification reaction time is 40~50 minutes.
Among the step c, the double alkalisation reaction times is 20~40 minutes, and the double alkalisation temperature of reaction is 20~40 ℃.
The secondary etherification reaction temperature is 80 ℃ ± 2 ℃ in the steps d, and the secondary etherification reaction time is 40~70 minutes.
The time that step e continues reaction is 40-50 minute.
Described potassium hydroxide solid adopts technical grade potassium hydroxide solid.
Described etherification reaction will carry out in 40 minutes after quaternization, mainly contains two purposes like this, and one is that etherifying agent Mono Chloro Acetic Acid and sodium hydroxide fully react formation sodium salt participation etherification reaction; The secondth, allow etherifying agent fully in soda cellulose, disperse infiltration, form parcel shape material to prevent local reaction, cause reaction inhomogeneous, cause the product inner quality poor.
The inventive method production process technology is simple, and reaction time is short, and facility investment is few, and raw material consumption is low, and the carboxymethyl cellulose potassium that adopts this method to produce not only has good solubility, and it has higher substitution degree simultaneously.Especially adopting the double alkalisation etherificate, mainly is to consider that in the production process of carboxymethyl cellulose potassium, potassium atom is not easy to replace on the products molecule chain, and adopts the double alkalisation etherificate can improve the product substitution value greatly, and then improves the performance of product.
Embodiment
The present invention is further illustrated below in conjunction with embodiment.
Embodiment 1:
With a certain amount of purified cotton that tears up, 2.0 48% potassium hydroxide aqueous solution doubly, 0.05 times potassium hydroxide solid and 1.8 times of ethanolic solns drop in the kneader simultaneously, stir alkalization after 80 minutes, 1.1 times of chloroacetic ethanolic solns are sprayed equably to kneader, carry out carboxymethylation reaction.Temperature is increased to 60-90 ℃, continue reaction 40 minutes, obtain rough modified carboxy methyl cellulose potassium, through washing, neutralization, centrifugal, dry, obtain making with extra care carboxymethyl cellulose potassium finished product after pulverizing, substitution value is 0.65, and 1% solution viscosity that NDJ-79 type viscometer is measured is 600mPas.Above multiple all is the amounts based on purified cotton.
Embodiment 2:
With a certain amount of purified cotton that tears up, 1.9 48% potassium hydroxide aqueous solution doubly, 0.1 times potassium hydroxide solid and 1.8 times of ethanolic solns drop in the kneader simultaneously, stir alkalization after 80 minutes, 1.1 times of chloroacetic ethanolic solns are sprayed equably to kneader, carry out carboxymethylation reaction.Temperature is increased to 60-90 ℃, continue reaction 40 minutes, obtain rough modified carboxy methyl cellulose potassium, through washing, neutralization, centrifugal, dry, obtain making with extra care carboxymethyl cellulose potassium finished product after pulverizing, substitution value is 0.68, and 1% solution viscosity that NDJ-79 type viscometer is measured is 620mPas.Above multiple all is the amounts based on purified cotton.
Embodiment 3:
With a certain amount of purified cotton that tears up, 2.7 doubly 48% potassium hydroxide aqueous solution, potassium hydroxide solid and 1.8 times of ethanolic solns of 0.1 times drop in the kneader simultaneously, stir alkalization after 80 minutes, 1.5 times of chloroacetic ethanolic solns are sprayed equably to kneader, carry out carboxymethylation reaction.Temperature is increased to 60-90 ℃, continue reaction 40 minutes, obtain rough modified carboxy methyl cellulose potassium, through washing, neutralization, centrifugal, dry, obtain making with extra care carboxymethyl cellulose potassium finished product after pulverizing, substitution value is 0.70, and 1% solution viscosity that NDJ-79 type viscometer is measured is 310mPas.Above multiple all is the amounts based on purified cotton.
Embodiment 4:
With a certain amount of purified cotton that tears up, 1.9 doubly 48% potassium hydroxide aqueous solution, potassium hydroxide solid and 1.8 times of ethanolic solns of 0.3 times drop in the kneader simultaneously, stir alkalization after 80 minutes, 1.4 times of chloroacetic ethanolic solns are sprayed equably to kneader, carry out carboxymethylation reaction.Temperature is increased to 60-90 ℃, continue reaction 40 minutes, obtain rough modified carboxy methyl cellulose potassium, through washing, neutralization, centrifugal, dry, obtain making with extra care carboxymethyl cellulose potassium finished product after pulverizing, substitution value is 0.80, and 1% solution viscosity that NDJ-79 type viscometer is measured is 530 mPas.Above multiple all is the amounts based on purified cotton.
Embodiment 5:
With a certain amount of purified cotton that tears up, earlier with 1.5 times of 48% potassium hydroxide aqueous solution, 0.15 potassium hydroxide solid doubly and 1.5 times of ethanolic solns drop in the kneader simultaneously, stir alkalization after 60 minutes, 0.9 times of chloroacetic ethanolic soln is sprayed equably to kneader, stirring reaction 40min, and then with 0.5 times of 48% potassium hydroxide aqueous solution, 0.15 potassium hydroxide solid doubly and 1.5 times of ethanolic solns drop in the kneader simultaneously, after alkalizing once more 30 minutes, again 0.5 times of chloroacetic ethanolic soln is sprayed equably to kneader, temperature is increased to 60-90 ℃, continue reaction 40 minutes, obtain rough modified carboxy methyl cellulose potassium, through washing, neutralization, centrifugal, dry, obtain refining carboxymethyl cellulose potassium finished product after the pulverizing, substitution value is 0.84, and 1% solution viscosity that NDJ-79 type viscometer is measured is 1015mPas.Above multiple all is the amounts based on purified cotton.
Embodiment 6:
With a certain amount of purified cotton that tears up, earlier with 1.4 times of 48% potassium hydroxide aqueous solution, 0.20 potassium hydroxide solid doubly and 1.5 times of ethanolic solns drop in the kneader simultaneously, stir alkalization after 60 minutes, 0.9 times of chloroacetic ethanolic soln is sprayed equably to kneader, stirring reaction 40min, and then with 0.5 times of 48% potassium hydroxide aqueous solution, 0.15 potassium hydroxide solid doubly and 1.5 times of ethanolic solns drop in the kneader simultaneously, after alkalizing once more 30 minutes, again 0.5 times of chloroacetic ethanolic soln is sprayed equably to kneader, temperature is increased to 60-90 ℃, continue reaction 40 minutes, obtain rough modified carboxy methyl cellulose potassium, through washing, neutralization, centrifugal, dry, obtain refining carboxymethyl cellulose potassium finished product after the pulverizing, substitution value is 0.85, and 1% solution viscosity that NDJ-79 type viscometer is measured is 890mPas.Above multiple all is the amounts based on purified cotton.
Embodiment 7:
With a certain amount of purified cotton that tears up, earlier with 1.4 times of 48% potassium hydroxide aqueous solution, 0.20 potassium hydroxide solid doubly and 1.5 times of ethanolic solns drop in the kneader simultaneously, stir alkalization after 60 minutes, 1.0 times of chloroacetic ethanolic solns are sprayed equably to kneader, stirring reaction 40min, and then with 0.5 times of 48% potassium hydroxide aqueous solution, 0.15 potassium hydroxide solid doubly and 1.5 times of ethanolic solns drop in the kneader simultaneously, after alkalizing once more 30 minutes, again 0.5 times of chloroacetic ethanolic soln is sprayed equably to kneader, temperature is increased to 60-90 ℃, continue reaction 40 minutes, obtain rough modified carboxy methyl cellulose potassium, through washing, neutralization, centrifugal, dry, obtain refining carboxymethyl cellulose potassium finished product after the pulverizing, substitution value is 0.87, and 1% solution viscosity that NDJ-79 type viscometer is measured is 780mPas.Above multiple all is the amounts based on purified cotton.
Embodiment 8:
With a certain amount of purified cotton that tears up, earlier with 1.4 times of 48% potassium hydroxide aqueous solution, 0.20 potassium hydroxide solid doubly and 1.5 times of ethanolic solns drop in the kneader simultaneously, stir alkalization after 60 minutes, 1.1 times of chloroacetic ethanolic solns are sprayed equably to kneader, stirring reaction 40min, and then with 0.5 times of 48% potassium hydroxide aqueous solution, 0.15 potassium hydroxide solid doubly and 1.5 times of ethanolic solns drop in the kneader simultaneously, after alkalizing once more 30 minutes, again 0.6 times of chloroacetic ethanolic soln is sprayed equably to kneader, temperature is increased to 60-90 ℃, continue reaction 40 minutes, obtain rough modified carboxy methyl cellulose potassium, through washing, neutralization, centrifugal, dry, obtain refining carboxymethyl cellulose potassium finished product after the pulverizing, substitution value is 0.89, and 1% solution viscosity that NDJ-79 type viscometer is measured is 760mPas.Above multiple all is the amounts based on purified cotton.
Term:
Viscosity: 1% aqueous solution, NDJ-79 type rotary viscometer detects under 25 ℃ of conditions.
Substitution value (D.S): detect according to 5.5 methods among the GB 1904-2005 " foodstuff additive Xylo-Mucine ", wherein in the substitution value calculation formula numerical value 0.08 to change numerical value be 0.096.

Claims (9)

1. the preparation method of a carboxymethyl cellulose potassium is characterized in that may further comprise the steps:
A, with purified cotton and potassium hydroxide aqueous solution and the potassium hydroxide solid pulverized, drop into together with aqueous ethanolic solution and to carry out a quaternization in the kneader;
After b, alkalization finish, etherifying agent is sprayed in the material to the kneader, carry out etherification reaction one time;
E, temperature are increased to 60-90 ℃, continue reaction, obtain rough modified carboxy methyl cellulose potassium, through washing, neutralization, centrifugal, dry, obtain making with extra care carboxymethyl cellulose potassium finished product after pulverizing;
The mass percent concentration of described potassium hydroxide aqueous solution is 40~55%, is reaction medium with the aqueous ethanolic solution, and the mass percentage concentration of aqueous ethanolic solution is 70~98%; Described etherifying agent is chloroacetic ethanolic soln, and its mass percent concentration is 50~80%;
Potassium hydroxide solid and purified cotton mass ratio 0.05~0.3:1;
Mass ratio 1.8~3.0:1 of potassium hydroxide solution and purified cotton;
Mass ratio 1.5~3.0:1 of aqueous ethanolic solution and purified cotton;
Mass ratio 1.0~1.7:1 of etherifying agent and purified cotton.
2. the preparation method of a carboxymethyl cellulose potassium is characterized in that may further comprise the steps:
A, with purified cotton and potassium hydroxide aqueous solution and the potassium hydroxide solid pulverized, drop into together with aqueous ethanolic solution and to carry out a quaternization in the kneader;
After b, alkalization finish, etherifying agent is sprayed in the material to the kneader, carry out etherification reaction one time;
After c, etherification reaction finish,, drop in the material in the kneader together with aqueous ethanolic solution and to carry out the double alkalisation reaction once more with potassium hydroxide aqueous solution and technical grade potassium hydroxide solid;
Add etherifying agent once more after d, the double alkalisation reaction, carry out the secondary etherification reaction;
E, temperature are increased to 60-90 ℃, continue reaction, obtain rough modified carboxy methyl cellulose potassium, through washing, neutralization, centrifugal, dry, obtain making with extra care carboxymethyl cellulose potassium finished product after pulverizing;
The mass percent concentration of described potassium hydroxide aqueous solution is 40~55%, is reaction medium with the aqueous ethanolic solution, and the mass percentage concentration of aqueous ethanolic solution is 70~98%; Described etherifying agent is chloroacetic ethanolic soln, and its mass percent concentration is 50~80%;
Potassium hydroxide solid and purified cotton mass ratio 0.05~0.3:1;
Mass ratio 1.8~3.0:1 of potassium hydroxide solution and purified cotton;
Mass ratio 1.5~3.0:1 of aqueous ethanolic solution and purified cotton;
Mass ratio 1.0~1.7:1 of etherifying agent and purified cotton.
3. the method for preparing carboxymethyl cellulose potassium according to claim 1 and 2 is characterized in that: a quaternization time is 50~80 minutes among the step a, and one time the quaternization temperature is 10~40 ℃.
4. the method for preparing carboxymethyl cellulose potassium according to claim 1 and 2 is characterized in that: an etherification reaction temperature is 80 ℃ ± 2 ℃ among the step a, and an etherification reaction time is 40~50 minutes.
5. the method for preparing carboxymethyl cellulose potassium according to claim 2 is characterized in that: among the step c, the double alkalisation reaction times is 20~40 minutes, and the double alkalisation temperature of reaction is 20~40 ℃.
6. the method for preparing carboxymethyl cellulose potassium according to claim 2 is characterized in that: the secondary etherification reaction temperature is 80 ℃ ± 2 ℃ in the steps d, and the secondary etherification reaction time is 40~70 minutes.
7. the method for preparing carboxymethyl cellulose potassium according to claim 1 and 2 is characterized in that: the time that step e continues reaction is 40~50 minutes.
8. the method for preparing carboxymethyl cellulose potassium according to claim 1 and 2 is characterized in that: described etherification reaction will carry out in 40 minutes after quaternization.
9. the method for preparing carboxymethyl cellulose potassium according to claim 1 and 2 is characterized in that: described potassium hydroxide solid adopts technical grade potassium hydroxide solid.
CN2011101943841A 2011-07-12 2011-07-12 Method for preparing potassium carboxymethylcellulose Active CN102286108B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2011101943841A CN102286108B (en) 2011-07-12 2011-07-12 Method for preparing potassium carboxymethylcellulose

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2011101943841A CN102286108B (en) 2011-07-12 2011-07-12 Method for preparing potassium carboxymethylcellulose

Publications (2)

Publication Number Publication Date
CN102286108A true CN102286108A (en) 2011-12-21
CN102286108B CN102286108B (en) 2012-11-28

Family

ID=45332880

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2011101943841A Active CN102286108B (en) 2011-07-12 2011-07-12 Method for preparing potassium carboxymethylcellulose

Country Status (1)

Country Link
CN (1) CN102286108B (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104082093A (en) * 2014-06-16 2014-10-08 郎溪县双明生态农业有限公司 Lagerstroemia transplanting method
CN104082092A (en) * 2014-06-16 2014-10-08 郎溪县双明生态农业有限公司 Transporting method for tallow trees
CN104082091A (en) * 2014-06-16 2014-10-08 郎溪县双明生态农业有限公司 Method for transplanting dragon juniper in summer
CN104098781A (en) * 2014-06-20 2014-10-15 华中农业大学 Method utilizing tabasheer waste to produce degradable liquid mulching film
CN104119454A (en) * 2013-12-02 2014-10-29 上海长光企业发展有限公司 Preparation method of polyanionic cellulose
CN104592398A (en) * 2015-02-03 2015-05-06 重庆力宏精细化工有限公司 Method for preparing sodium carboxymethyl cellulose
CN104592399A (en) * 2015-02-03 2015-05-06 重庆力宏精细化工有限公司 Preparation method for improving free fiber yarn contained in sodium carboxymethyl cellulose water solution
CN105254769A (en) * 2015-11-24 2016-01-20 泸州北方化学工业有限公司 Method for preparing technical grade sodium carboxymethyl cellulose
CN105330752A (en) * 2015-11-24 2016-02-17 泸州北方化学工业有限公司 Method for preparing sodium carboxymethyl cellulose with high degree of substitution
CN106336461A (en) * 2016-08-22 2017-01-18 四川北方硝化棉股份有限公司 Preparation method of carboxymethyl cellulose lithium
CN112707969A (en) * 2020-12-28 2021-04-27 常熟威怡科技有限公司 Production process of sodium carboxymethylcellulose by self-esterification reaction

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1459464A (en) * 2002-05-23 2003-12-03 武汉理工大学 Preparation method of water soluble hydroxyethyl carboxymethyl cellulose thickener
US20070249825A1 (en) * 2006-04-21 2007-10-25 Sau Arjun C Decolorized raw cotton linters and preparation of ether derivatives therefrom

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1459464A (en) * 2002-05-23 2003-12-03 武汉理工大学 Preparation method of water soluble hydroxyethyl carboxymethyl cellulose thickener
US20070249825A1 (en) * 2006-04-21 2007-10-25 Sau Arjun C Decolorized raw cotton linters and preparation of ether derivatives therefrom

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104119454A (en) * 2013-12-02 2014-10-29 上海长光企业发展有限公司 Preparation method of polyanionic cellulose
CN104082092A (en) * 2014-06-16 2014-10-08 郎溪县双明生态农业有限公司 Transporting method for tallow trees
CN104082091A (en) * 2014-06-16 2014-10-08 郎溪县双明生态农业有限公司 Method for transplanting dragon juniper in summer
CN104082093A (en) * 2014-06-16 2014-10-08 郎溪县双明生态农业有限公司 Lagerstroemia transplanting method
CN104098781B (en) * 2014-06-20 2016-08-17 华中农业大学 A kind of method utilizing Concretio silicea Bambusae seu schizostachyi waste material to produce degradable liquid mulch film
CN104098781A (en) * 2014-06-20 2014-10-15 华中农业大学 Method utilizing tabasheer waste to produce degradable liquid mulching film
CN104592398A (en) * 2015-02-03 2015-05-06 重庆力宏精细化工有限公司 Method for preparing sodium carboxymethyl cellulose
CN104592399A (en) * 2015-02-03 2015-05-06 重庆力宏精细化工有限公司 Preparation method for improving free fiber yarn contained in sodium carboxymethyl cellulose water solution
CN105254769A (en) * 2015-11-24 2016-01-20 泸州北方化学工业有限公司 Method for preparing technical grade sodium carboxymethyl cellulose
CN105330752A (en) * 2015-11-24 2016-02-17 泸州北方化学工业有限公司 Method for preparing sodium carboxymethyl cellulose with high degree of substitution
CN106336461A (en) * 2016-08-22 2017-01-18 四川北方硝化棉股份有限公司 Preparation method of carboxymethyl cellulose lithium
CN106336461B (en) * 2016-08-22 2018-09-11 四川北方硝化棉股份有限公司 A kind of preparation method of carboxymethyl cellulose lithium
CN112707969A (en) * 2020-12-28 2021-04-27 常熟威怡科技有限公司 Production process of sodium carboxymethylcellulose by self-esterification reaction

Also Published As

Publication number Publication date
CN102286108B (en) 2012-11-28

Similar Documents

Publication Publication Date Title
CN102286108B (en) Method for preparing potassium carboxymethylcellulose
CN101280023B (en) Preparation of acid-resistant sodium carboxymethylcellulose
CN101003577B (en) Technique for producing polyanionic cellulose with high degree of substitution
CN102675474B (en) Preparation method of ultrahigh-viscosity sodium carboxymethyl cellulose
NZ700627A (en) Method for the preparation of cellulose ethers with a high solids process, product obtained and uses of the product
CN102718874B (en) Method for preparing methyl cellulose ether with arundodomax dissolving pulp serving as raw material
CN104087283A (en) Fracturing thickening agent for fast dispersing and tackifying under acidic condition and preparation method thereof
CN103772558B (en) A kind of preparation method of low viscosity poly hydrolyzate fluid loss agent
CN102583366A (en) Method for washing active carbon with low water consumption
JP2015057270A (en) Granulating agent for slag
CN101434658A (en) Method for producing carboxymethyl cellulose from cotton stem
CN104403057B (en) Fluid loss additive for boring fluid and preparation method thereof and application
CN105283523A (en) Fracturing fluid viscosity-controlling agent to be used in hydraulic fracturing
CN103275240B (en) Crosslinking-oxidization tara gum and preparation method thereof
CN101993499A (en) Method for producing carboxymethylcellulose
CN103087201A (en) Production technology for preparing hyperviscous industrial-grade cellulose glycolate by means of half aqueous medium process
CN105111317A (en) Preparation method of cellulose ether and cellulose ether obtained in same
CN104004501A (en) Composite active enzymic preparation and method for preparing lignite oil field drilling fluid filtrate reducer
CN104558219A (en) Preparation method of cationic corn starch
CN114920852A (en) Heat-resistant salt-tolerant polyanionic cellulose and preparation method thereof
CN101108962A (en) Multifunctional drilling fluid additive
CN101440132A (en) Preparation of technology level sodium carboxymethylcellulose
CN105482787A (en) Kneading method for preparing water-based drilling fluid filtrate reducer by using anaerobic fermentation biogas residues
CN101798504A (en) Multi-effect thickening agent for fracturing and preparation method thereof
CN103950910B (en) A kind of reaction extrusion process produces the method for barium phosphate

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant