CN1792960A - Maleic acid anhydride series concrete water-reducing agent and preparation process thereof - Google Patents

Maleic acid anhydride series concrete water-reducing agent and preparation process thereof Download PDF

Info

Publication number
CN1792960A
CN1792960A CN 200510019876 CN200510019876A CN1792960A CN 1792960 A CN1792960 A CN 1792960A CN 200510019876 CN200510019876 CN 200510019876 CN 200510019876 A CN200510019876 A CN 200510019876A CN 1792960 A CN1792960 A CN 1792960A
Authority
CN
China
Prior art keywords
maleic anhydride
reducing agent
concrete water
series concrete
preparation
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
CN 200510019876
Other languages
Chinese (zh)
Other versions
CN1330600C (en
Inventor
马保国
谭洪波
潘伟
董荣珍
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wuhan University of Technology WUT
Original Assignee
Wuhan University of Technology WUT
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Wuhan University of Technology WUT filed Critical Wuhan University of Technology WUT
Priority to CNB2005100198761A priority Critical patent/CN1330600C/en
Publication of CN1792960A publication Critical patent/CN1792960A/en
Application granted granted Critical
Publication of CN1330600C publication Critical patent/CN1330600C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

A maleic anhydride series water-reducing agent for concrete is prepared through reaction between methoxy polyethanediol and maleic anhydride to generate monomethoxy polyethanediol maleate, and copolymerizing on 2-acrylamide-2-sodium methylpropyl sulfonate. Its advantages are high water-reducing effect, low content of alkali, and high flowability and low slump of concrete.

Description

A kind of maleic anhydride series concrete water-reducing agent and preparation method
Technical field
The invention belongs to a kind of preparation method of maleic anhydride series concrete water-reducing agent.
Technical background
As everyone knows, when the cement mixture operation, effective for making rapid operation, and the early stage demoulding requires cement mixture to have high workability with the reduction of erection time, effectively the loss of inhibition of slump, and there is sufficient early strength at the sclerosis initial stage, and this just needs a kind of high performance concrete water reducer.Along with the concrete the reach of science, polymer chemistry and material molecule design theory constantly make further progress, and cement water reducing agent is also had higher requirement.And the cement water reducing agent of China is a product based on naphthalene system and melamine at present, and the cement mixture workability of this series products is bad, has the problem that water-reducing rate is not high, slump-loss is big.Though use water-soluble ethylene copolymer cement dispersant slump-loss little, prolong time of coagulation greatly, causes early strength low, can not well satisfy the needs of engineering, and complex manufacturing.Domestic closely during the last ten years, the research and development main products of new and effective water reducer and superplasticizer still is naphthalenesulfonate formaldehyde condensation compound and sulfamate condenses etc., and to polycarboxylic acid series, no matter the research of maleic anhydride based water reducer is to select from starting material, production technique or raising aspect of performance are all started late, though domestic investigator explores polycarboxylic acid series by molecular pathways, maleic anhydride based water reducer product has been obtained certain effect, but it is domestic to polycarboxylic acid series, the research and development of maleic anhydride based water reducer product are in the experiment development stage mostly, the producer of real formation product also seldom far can not satisfy the needs of high performance concrete development.And maleic anhydride series, the vinylformic acid system high-performance water reducing agent of the development of states such as Japan have high water reducing rate, and numerous premium propertiess such as low slump loss have obtained using widely, and technology is ripe.
The synthetic method of Japan report maleic anhydride high performance concrete water reducer was divided into for two steps and finishes.The first step: behind the nitrogen purge autoclave; under the nitrogen protection condition; make catalyzer with sodium methylate; slowly feed oxyethane in the methyl alcohol in reaction vessel, keep 140 ℃, the reaction down of 0.05-0.5 MPa pressure, then; reaction mixture is cooled to room temperature; in reaction vessel, add NaOH, be warming up to 110 ℃, keep the dehydration of 20mmHg pressure.Subsequently, nitrogen pressure is increased to 0.1 MPa, slowly in mixture, add a certain amount of chlorallylene and stirring.After 4 hours, when mixture basicity is reduced to a stationary value, use the HCl neutralise mixt from the reaction beginning, the separating by-products salt can obtain allyl ethers, as the raw material of next step reaction.Second the step: with toluene as solvent; under nitrogen protection; in having the reaction vessel of condensation; the allyl ethers and the maleic anhydride that are generated with the first step reaction carry out polyreaction; polymerization temperature is 80 ℃, stir make it to react 4 hours after, under 110 ℃, 10mmHg pressure; steam and remove toluene solvant, obtaining transparent viscous liquid is final product.Introduce among the Te Kaiping 9-286648, taking by weighing polyoxyethylene (oxyethane) 33mol, monomethyl monoallyl ether 1mol, allyl sodium sulfonate 1mol and Maleic Acid, Anhydrous 3mol in the four-hole boiling flask that agitator, thermometer, prolong, nitrogen ingress pipe are housed is dissolved in the 1480g water, add ammonium persulphate 0.75mol as polymerization starter, 50 ± 2 ℃ were reacted 12 hours under nitrogen atmosphere, obtained interpolymer X.
This shows, maleic anhydride series high-performance cement water reducing agent process for producing complexity, severe reaction conditions is wayward, and is very high to equipment requirements, is unfavorable for industrial production.
Summary of the invention:
The objective of the invention is to overcome water reducer complex manufacturing in the past, to the equipment requirements height, a kind of preparation method of maleic anhydride series concrete water-reducing agent is provided, have polymolecularity and disperse retentivity with this method synthetic water reducer, and synthesis technique is simple, reaction conditions is simple and easy to control, do not pollute, cost hangs down advantages such as being easy to suitability for industrialized production.
The present invention realizes by the following technical solutions:
A kind of maleic anhydride series concrete water-reducing agent, its molecular weight are 10000~60000, and its molecular formula is:
In the formula: m=6~23
n=10~60
Above-mentioned molecular formula represents it is the molecular structure of using present method synthetic maleic anhydride series concrete water-reducing agent, its synthesis technique was divided into for two steps, the first step: with maleic anhydride and methoxy poly (ethylene glycol) mol ratio is to be raw material at 1.1~1.8: 1, make catalyzer at tosic acid, cuprous chloride and Resorcinol are made stopper, toluene is done to react under the condition of solvent, 80~120 ℃ of controlled temperature react and generated toxilic acid mono methoxy polyethylene glycol ester and the big monomer mixture of toxilic acid Varonic DM 55 ester in 10~15 hours;
In the formula: m=6~23
Second step: use ammonium persulphate as initiator, mercaptoethanol is as chain-transfer agent, the mass ratio that slowly adds on one side big monomer mixture that the first step obtains and 2-acrylamide-2 methyl-propyl sodium sulfonate is 17.5~31: 1 mixed aqueous solution, slowly add initiator and chain-transfer agent on one side, controlled temperature is intact to adding material at 80~85 ℃, then 80~85 ℃ of insulations 1 hour, temperature is elevated to 95~100 ℃ of insulations 2 hours, be cooled to 15~30 ℃ of room temperatures, neutralizing with sodium hydroxide, to obtain mass concentration be 30% the high-molecular copolymer aqueous solution in pH=6.5 ± 0.5, be the cement water reducing agent that present method makes, the principal reaction formula is:
In the formula: m=6~23
n=10~60。
The first step catalyzer tosic acid consumption is 2%~8% of maleic anhydride and a methoxy poly (ethylene glycol) total mass; The hydroquinone of polymerization retarder consumption is 0.5%~2% of a maleic anhydride quality, and the cuprous chloride consumption is 0.5%~1.5% of a maleic anhydride quality; Reaction solvent toluene consumption is 80%~150% of maleic anhydride and a methoxy poly (ethylene glycol) total mass; The second step polymerization is 1.8%~8% of maleic acid ester and 2-acrylamide-2 a methyl-propyl sodium sulfonate monomer total mass with initiator ammonium sulfate quality; Polymerization is 0.1%~2% of maleic acid ester and 2-acrylamide-2 a methyl-propyl sodium sulfonate monomer total mass with chain-transfer agent mercaptoethanol quality; The aqueous solution, the chain-transfer agent mercaptoethanol aqueous solution and the initiator ammonium persulfate aqueous solution of big monomer mixture and 2-acrylamide-2 methyl-propyl sodium sulfonate slowly added at 2.5~3.5 hours in second step.
Maleic anhydride series concrete water-reducing agent of the present invention is to be reacted under certain condition by methoxy poly (ethylene glycol) and maleic anhydride to generate the big monomer of maleic acid ester, utilize the synthetic carboxyl that contains of big monomer of synthetic and the copolymerization of 2-acrylamide-2 methyl-propyl sodium sulfonate, sulfonic group, the polymer of polyoxyethylene chain side chain.Need not nitrogen protection in the building-up process, the temperature of reaction substantially constant, reinforced program is simple, and reaction conditions is easy to control; And cost is lower than the acrylic acid series cement water reducing agent.The maleic anhydride series concrete water-reducing agent that adopts the inventive method to make, volume (mass concentration is 30% maleic anhydride series concrete water-reducing agent) is at 1.0% o'clock of cement weight, water-reducing rate can reach 30%; The concrete surface of preparation does not have bleeding line, no air pocket, aberration is little, Surface Quality of Concrete good; Alkali content is low; Chloride ion-containing not is to the reinforcing bar non-corrosiveness; Freeze-thaw-ability and anti-carbonization ability significantly improve than normal concrete; Can effectively restrain hydration heat, prevent the inner cracking that heats up; Concrete 28d shrinking percentage is that analog high efficiency water reducing agent reduces more than 20% than naphthalene; The adaptation of product is strong, is adapted to the cement of plurality of specifications, model, and especially suitable and high-quality fly ash, the compatible preparation of slag isoreactivity adulterant are high-strength, high-durability, the contour performance concrete of self-compacting; Product is aqueous solution stable performance, and long storage is not stratified, do not have precipitation, do not have crystallization winter, nontoxic pollution-free, advantage such as environmentally safe.
Embodiment
Embodiment 1~7
Toxilic acid mono methoxy polyethylene glycol ester and toxilic acid Varonic DM 55 ester are big monomeric synthetic:
Press listed each inventory in the table 1, take by weighing maleic anhydride, methoxy poly (ethylene glycol), Resorcinol, cuprous chloride, tosic acid, toluene (seeing Table 1) respectively and put into there-necked flask, be heated with stirring to 62.5 ± 2.5 ℃, wait to dissolve complete back insulation 0.75 ± 0.25 hour, slowly be warming up to 85 ± 5 ℃ again, insulation reaction 4.5 ± 0.5 hours is warming up to 115 ± 5 ℃ again, insulation reaction 7 ± 1 hours; Be cooled to 20 ± 5 ℃ of room temperatures, remove solvent toluene, obtain toxilic acid mono methoxy polyethylene glycol ester and the big monomer of toxilic acid Varonic DM 55 ester.
Table 1 each reactant consumption in big monomeric synthesizing
Embodiment number Maleic anhydride (g) Methoxy poly (ethylene glycol) (1000) (g) Resorcinol (g) Cuprous chloride (g) Tosic acid (g) Toluene (g)
1 10.8 100 0.21 0.11 4.43 132
2 14.7 100 0.29 0.15 4.59 137
3 17.6 100 0.35 0.18 4.70 141
4 14.7 100 0.44 0.08 4.59 137
5 14.7 100 0.08 0.22 4.59 137
6 14.7 100 0.29 0.14 2.29 137
7 14.7 100 0.29 0.14 4.59 92.8
Embodiment 8~12
Maleic anhydride series concrete water-reducing agent high molecular polymerization:
Press listed each inventory in the table 2, taking by weighing the dissolving of toxilic acid mono methoxy polyethylene glycol ester and the big monomer of toxilic acid Varonic DM 55 ester, 2-acrylamide-2 methyl-propyl sodium sulfonate respectively, to be mixed with mass concentration be 60% the aqueous solution, as titrating solution 1; Take by weighing the ammonium persulphate dissolving and be mixed with the aqueous solution, as titrating solution 2; Take by weighing mercaptoethanol and be mixed with the aqueous solution, as titrating solution 3 (each material consumption sees Table 2).Put into suitable quantity of water in the there-necked flask, stirring heating keeps 82.5 ± 2.5 ℃, and slowly titrating solution 1 and titrating solution 2 treat that polyreaction began the back about 0.4 ± 0.1 hour, and beginning slowly drips titrating solution 3, and speed is dripped in control, all drips off in 3.0 ± 0.5 hours; 82.5 ± 2.5 ℃ of time insulations are 1 hour then, are warming up to 97.5 ± 2.5 ℃ again, are incubated 2 hours, are cooled to 20 ± 5 ℃ of room temperatures then, and neutralizing with sodium hydroxide, to obtain mass concentration be 30% the high-molecular copolymer aqueous solution in pH=6.5 ± 0.5.
Table 2 polymerizable maleimide acid anhydride series concrete water-reducing agent is with each reactant consumption
Embodiment number The big monomer of maleic acid ester (g) 2-acrylamide-2 methyl-propyl sodium sulfonate (g) Ammonium persulphate (g) Mercaptoethanol (g) Water (g)
8 (17.5 embodiment 3 in the table 1) 1.0 0.93 0.19 45.76
9 (25.0 embodiment 4 in the table 1) 1.0 1.30 0.26 64.31
10 (31.0 embodiment 5 in the table 1) 1.0 1.60 0.32 79.15
11 (25.0 embodiment 6 in the table 1) 1.0 0.78 0.13 62.79
12 (25.0 embodiment 7 in the table 1) 1.0 1.82 0.34 65.70
With the inventive method synthetic high-molecular copolymer is that the maleic anhydride series concrete water-reducing agent has dispersed preferably and the dispersion retentivity.Carry out the quiet slurry test of cement with national standard, volume is 0.15% o'clock of solid content quality, and quiet slurry degree of mobilization lost greater than 250mm in 1 hour hardly, loss 20~30% in 4 hours (the quiet slurry of cement is tested with little wild field 525 silicate cements).Mixing mass concentration of the present invention in concrete is 30% maleic anhydride series concrete water-reducing agent, and volume is 1.0% o'clock of gelling material quality, and water-reducing rate can be up to 30%.

Claims (8)

1. maleic anhydride series concrete water-reducing agent, the molecular weight that it is characterized in that is 10000~60000, molecular formula is:
Figure A2005100198760002C1
In the formula: m=6~23
n=10~60
2. the preparation method of the described maleic anhydride series concrete water-reducing agent of claim 1, it is characterized in that: synthesis technique was divided into for two steps,
The first step: with maleic anhydride and methoxy poly (ethylene glycol) mol ratio is to be raw material at 1.1~1.8: 1, make catalyzer at tosic acid, cuprous chloride and Resorcinol are made stopper, toluene is done to react under the condition of solvent, 80~120 ℃ of controlled temperature, reacted 10~15 hours, solvent toluene is removed in cooling, obtains toxilic acid mono methoxy polyethylene glycol ester and the big monomer mixture of toxilic acid Varonic DM 55 ester;
Second step: use ammonium persulphate as initiator, mercaptoethanol is as chain-transfer agent, the mass ratio that slowly adds on one side big monomer mixture that the first step obtains and 2-acrylamide-2 methyl-propyl sodium sulfonate is 17.5~31: 1 mixed aqueous solution, slowly add initiator and chain-transfer agent on one side, controlled temperature is intact to adding material at 80~85 ℃, then 80~85 ℃ of insulations 1 hour, temperature is elevated to 95~100 ℃ of insulations 2 hours, be cooled to 15~30 ℃ of room temperatures, neutralizing with sodium hydroxide, to obtain mass concentration be 30% the high-molecular copolymer aqueous solution in pH=6.5 ± 0.5, is the maleic anhydride series concrete water-reducing agent that makes.
3. the preparation method of maleic anhydride series concrete water-reducing agent as claimed in claim 2 is characterized in that the catalyzer tosic acid consumption in the described the first step is 2%~8% of a total mass.
4. the preparation method of maleic anhydride series concrete water-reducing agent as claimed in claim 2, it is characterized in that the hydroquinone of polymerization retarder consumption in the described the first step is 0.5%~3% of a maleic anhydride quality, the cuprous chloride consumption is 0.5%~1.5% of a maleic anhydride quality.
5. the preparation method of maleic anhydride series concrete water-reducing agent as claimed in claim 2 is characterized in that the reaction solvent toluene consumption in the described the first step is 50%~150% of a total mass.
6. the preparation method of maleic anhydride series concrete water-reducing agent as claimed in claim 2 is characterized in that the initiator ammonium persulfate quality that polymerization is used in described second step is 1.8%~8% of maleic acid ester and 2-acrylamide-2 a methyl-propyl sodium sulfonate monomer mass.
7. the preparation method of maleic anhydride series concrete water-reducing agent as claimed in claim 2 is characterized in that the chain-transfer agent mercaptoethanol quality that polymerization is used in described second step is 0.1%~2% of maleic acid ester and 2-acrylamide-2 a methyl-propyl sodium sulfonate monomer mass.
8. the preparation method of maleic anhydride series concrete water-reducing agent as claimed in claim 2 is characterized in that the aqueous solution, the chain-transfer agent mercaptoethanol aqueous solution and the initiator ammonium persulfate aqueous solution of big monomer mixture and 2-acrylamide-2 methyl-propyl sodium sulfonate slowly added at 2.5~3.5 hours in described second step.
CNB2005100198761A 2005-11-24 2005-11-24 Maleic acid anhydride series concrete water-reducing agent and preparation process thereof Expired - Fee Related CN1330600C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2005100198761A CN1330600C (en) 2005-11-24 2005-11-24 Maleic acid anhydride series concrete water-reducing agent and preparation process thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2005100198761A CN1330600C (en) 2005-11-24 2005-11-24 Maleic acid anhydride series concrete water-reducing agent and preparation process thereof

Publications (2)

Publication Number Publication Date
CN1792960A true CN1792960A (en) 2006-06-28
CN1330600C CN1330600C (en) 2007-08-08

Family

ID=36804626

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2005100198761A Expired - Fee Related CN1330600C (en) 2005-11-24 2005-11-24 Maleic acid anhydride series concrete water-reducing agent and preparation process thereof

Country Status (1)

Country Link
CN (1) CN1330600C (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100465123C (en) * 2006-11-23 2009-03-04 河南理工大学 Method of preparing poly carboxylic acid series water reducer using maleic anhydride
CN101967369A (en) * 2010-08-16 2011-02-09 山东大学 Comb-like polymer fluid loss additive for drilling fluid and preparation method thereof
CN102532437A (en) * 2011-12-30 2012-07-04 上虞吉龙化学建材有限公司 Preparation method for high-performance polycarboxylic acid water-reducing and slump-retaining agent
CN103755895A (en) * 2013-12-19 2014-04-30 聊城大学 Polycarboxylic acid high performance water reducing agent and preparation method thereof
CN104129941A (en) * 2014-07-28 2014-11-05 武汉理工大学 Slump-retaining type polycarboxylic acid water reducing agent and preparation method thereof
CN104446239A (en) * 2014-11-12 2015-03-25 无为恒基商品混凝土有限公司 High-density freezing-tolerant concrete
CN104592506A (en) * 2014-11-24 2015-05-06 沈阳工业大学 N-methoxypolyethylene glycols-N,-carbamyl maleimide and preparation method thereof
CN105175740A (en) * 2015-08-25 2015-12-23 科之杰新材料集团有限公司 Preparation method of polycarboxylic acid water reducer with high workability
CN106242434A (en) * 2016-08-29 2016-12-21 蚌埠市宝运商品混凝土有限公司 A kind of highway is with high durability degree concrete
CN106496433A (en) * 2016-10-11 2017-03-15 常州市鼎升环保科技有限公司 A kind of preparation method of polycarboxylic acid super-plasticizer
CN107628789A (en) * 2017-09-25 2018-01-26 常州西夏墅东方工具有限公司 A kind of preparation method of fast solidifying soft rock injecting paste material
CN107641172A (en) * 2017-09-01 2018-01-30 沈阳工业大学 A kind of N maleimides N ethylsulfonic acids sodium and preparation method
CN112645630A (en) * 2020-12-19 2021-04-13 厦门宏发先科新型建材有限公司 Fluorine-containing early-strength polycarboxylate superplasticizer, preparation method thereof and early-strength concrete

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1093095C (en) * 2000-11-07 2002-10-23 复旦大学 Efficient carboxilic acid grafting water-reducing agent and its synthesis
US6858074B2 (en) * 2001-11-05 2005-02-22 Construction Research & Technology Gmbh High early-strength cementitious composition
JP4162192B2 (en) * 2002-05-17 2008-10-08 Basfポゾリス株式会社 Cement water reducing agent with excellent slump loss prevention
CN1600735A (en) * 2003-09-22 2005-03-30 北京绿色前缘技术创新中心有限公司 High performance cement dispersing agent in copolymerization carboxylic acids with side chain of poly alkylene glycol ether

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100465123C (en) * 2006-11-23 2009-03-04 河南理工大学 Method of preparing poly carboxylic acid series water reducer using maleic anhydride
CN101967369A (en) * 2010-08-16 2011-02-09 山东大学 Comb-like polymer fluid loss additive for drilling fluid and preparation method thereof
CN101967369B (en) * 2010-08-16 2013-01-02 山东大学 Comb-like polymer fluid loss additive for drilling fluid and preparation method thereof
CN102532437A (en) * 2011-12-30 2012-07-04 上虞吉龙化学建材有限公司 Preparation method for high-performance polycarboxylic acid water-reducing and slump-retaining agent
CN102532437B (en) * 2011-12-30 2013-08-07 上虞吉龙化学建材有限公司 Preparation method for high-performance polycarboxylic acid water-reducing and slump-retaining agent
CN103755895B (en) * 2013-12-19 2017-01-11 聊城大学 Polycarboxylic acid high performance water reducing agent and preparation method thereof
CN103755895A (en) * 2013-12-19 2014-04-30 聊城大学 Polycarboxylic acid high performance water reducing agent and preparation method thereof
CN104129941A (en) * 2014-07-28 2014-11-05 武汉理工大学 Slump-retaining type polycarboxylic acid water reducing agent and preparation method thereof
CN104446239A (en) * 2014-11-12 2015-03-25 无为恒基商品混凝土有限公司 High-density freezing-tolerant concrete
CN104592506A (en) * 2014-11-24 2015-05-06 沈阳工业大学 N-methoxypolyethylene glycols-N,-carbamyl maleimide and preparation method thereof
CN104592506B (en) * 2014-11-24 2017-01-18 沈阳工业大学 N-methoxypolyethylene glycols-N,-carbamyl maleimide and preparation method thereof
CN105175740A (en) * 2015-08-25 2015-12-23 科之杰新材料集团有限公司 Preparation method of polycarboxylic acid water reducer with high workability
CN106242434A (en) * 2016-08-29 2016-12-21 蚌埠市宝运商品混凝土有限公司 A kind of highway is with high durability degree concrete
CN106496433A (en) * 2016-10-11 2017-03-15 常州市鼎升环保科技有限公司 A kind of preparation method of polycarboxylic acid super-plasticizer
CN107641172A (en) * 2017-09-01 2018-01-30 沈阳工业大学 A kind of N maleimides N ethylsulfonic acids sodium and preparation method
CN107628789A (en) * 2017-09-25 2018-01-26 常州西夏墅东方工具有限公司 A kind of preparation method of fast solidifying soft rock injecting paste material
CN107628789B (en) * 2017-09-25 2020-08-11 嘉兴晟源工业设计有限公司 Preparation method of fast-setting soft rock grouting material
CN112645630A (en) * 2020-12-19 2021-04-13 厦门宏发先科新型建材有限公司 Fluorine-containing early-strength polycarboxylate superplasticizer, preparation method thereof and early-strength concrete

Also Published As

Publication number Publication date
CN1330600C (en) 2007-08-08

Similar Documents

Publication Publication Date Title
CN1330600C (en) Maleic acid anhydride series concrete water-reducing agent and preparation process thereof
CN1308257C (en) Water reducing agent of poly carboxylic acid series concrete and its preparation process
CN109987870B (en) High-efficiency concrete water reducing agent and preparation method thereof
CN101244907A (en) Polycarboxylic acids series concrete high efficiency water reducing agent and synthesizing process
CN101475664B (en) Preparation of polycarboxylic acid water reducing agent for prefabricated part
CN104017139B (en) The preparation method of a kind of poly-carboxylic high-performance cement water reducing agent
CN103265201B (en) Sorbitol modified polycarboxylate-type water reducing agent and synthetic method thereof
CN109575198B (en) Enhanced polycarboxylate superplasticizer and preparation method thereof
CN105601843A (en) Early-strength ethers polycarboxylic acid water reducing agent and preparation method thereof
CN103396028A (en) High-early-strength polycarboxylate water reducer and preparation method thereof
CN102161733A (en) Green preparation method of slow-release polycarboxylic-acid high-performance water reducing agent
CN101817657A (en) Polycarboxylic acid slump retaining agent
CN107337769B (en) Slump-retaining type polycarboxylate superplasticizer and preparation method thereof
CN108218284B (en) Concrete water reducing agent composition
CN107686540A (en) A kind of preparation method of Early-strength polycarboxylate superplasticizer
CN100465123C (en) Method of preparing poly carboxylic acid series water reducer using maleic anhydride
CN102718427B (en) Sulfonyl modified carboxylic acid water-reducing agent and preparation method thereof
CN102718426A (en) Modified carboxylic acid water-reducing agent and preparation method thereof
CN100360455C (en) Concrete water reducing agent of polyacrylic acid and its synthesis process
CN102503221B (en) Cyclohexanol grafted polycarboxylic acid water reducing agent and preparation method thereof
CN102951866A (en) Ascorbic acid modified carboxylic water reducer and preparation method thereof
CN1314614C (en) Concrete water reducing agent of polycarboxylic acid and its prepn process
CN102731730A (en) Hydrogen peroxide auxiliarily-initiated carboxylic acid water reducer and its preparation method
CN102503216A (en) Method for synthesizing universal polycarboxylic water reducer
CN100358825C (en) Acrylic acid series multiple copolymer analog high efficiency water reducing agent and its synthesis method

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20070808

Termination date: 20131124