Preparation method for synthesizing ultra-slow-release polycarboxylate superplasticizer from high-activity polyether

A technology of slow-release polycarboxylic acid and high-activity polyether, which is applied in the field of building material production, can solve the problems of long production cycle, short slow-release time, low reactivity, etc., and solve the problems of excessive collapse and open operation time , high reactivity

Inactive Publication Date: 2020-11-13
北京水木佳维新材料技术研究院有限公司
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AI Technical Summary

Problems solved by technology

At present, most slow-release polycarboxylate superplasticizers are synthesized with vinyl alcohol 4C (methallyl polyoxyethylene ether HPEG) and 5C (prenyl polyoxyethylene ether TPEG) macromonomers, which are subject to Influenced by the low reactivity of unsaturated double bonds, the polymerization reaction generally needs to be carried out under high temperature conditions. Although the redox agent initiation system realizes normal temperature polymerization, the reaction time is 3-5h, the production cycle is long, and the energy consumption is high.
[0004] Patent CN102503226B discloses a high-slump-retaining polycarboxylate water-reducer with slow-release effect and its preparation method, which introduces acrylamide monomers and (meth)acrylate monomers into polycarboxylates as slump-retaining aids. In the main chain of the acid molecule, the obtained water reducer has excellent slump retention performance, and the slump is basically not lost within 3 hours, but the reaction needs to be carried out at 60-80°C, the polymerization reaction time is as long as 5-7 hours, and the production energy consumption is too high ; Patent CN107325235A discloses a normal-temperature synthesis process of a slow-release polycarboxylate superplasticizer with a reaction temperature of 10-35°C. Compared with the traditional synthetic process of a slow-release polycarboxylate superplasticizer, the production method Simple and easy to operate, but because it is synthesized by monocarboxylic acid hydroxyalkyl ester, the sustained release time is relatively short, and affected by the reactivity of polyether macromonomers, there are also problems of long reaction time and high production energy consumption

Method used

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  • Preparation method for synthesizing ultra-slow-release polycarboxylate superplasticizer from high-activity polyether
  • Preparation method for synthesizing ultra-slow-release polycarboxylate superplasticizer from high-activity polyether
  • Preparation method for synthesizing ultra-slow-release polycarboxylate superplasticizer from high-activity polyether

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Effect test

Embodiment 1

[0027] S1: Adding solutions A and B: Mix 15 parts of acrylic acid, 20 parts of hydroxyethyl acrylate, 15 parts of hydroxypropyl acrylate, 35 parts of dimethyl fumarate, 2.5 parts of thioglycolic acid, and 55 parts of deionized water As dripping solution A; mix 2 parts of sodium bisulfite and 60.5 parts of deionized water evenly as dropping solution B, and set aside;

[0028] S2: Add 270 parts of deionized water and 300 parts of EPEG3000 monomer into the reactor, stir at room temperature to fully dissolve, adjust the temperature to 10°C, add 3 parts of acrylic acid to adjust the acidity of the bottom solution, and stir evenly;

[0029] S3: At the initial temperature of 10°C, add 5 parts of 1% ferric chloride solution and 3 parts of ammonium persulfate to the mixed solution obtained in step S2, stir for 5 minutes and start adding liquid A and liquid B at a constant speed, and add liquid A dropwise 50min, B solution was added dropwise for 60min, during which the temperature of th...

Embodiment 2

[0032] S1: Adding solutions A and B: Mix 15.5 parts of acrylic acid, 20.5 parts of hydroxyethyl acrylate, 13 parts of hydroxypropyl acrylate, 40 parts of dimethyl maleate, 1.5 parts of mercaptopropionic acid, and 55 parts of deionized water Uniformly used as dripping solution A; mix 0.9 parts of L-ascorbic acid and 81.5 parts of deionized water evenly as dropping solution B, and set aside;

[0033] S2: Add 250 parts of deionized water and 300 parts of EPEG3000 monomer into the reaction kettle, stir at room temperature to fully dissolve, adjust the temperature to 15°C, add 2.5 parts of acrylic acid to adjust the acidity of the bottom solution, and stir evenly;

[0034] S3: At the initial temperature of 15°C, add 2 parts of 1% ferrous sulfate solution and 3 parts of 30% hydrogen peroxide to the mixed solution obtained in step S2, stir for 5 minutes and start adding liquid A and liquid B dropwise at a constant speed, and add liquid A dropwise 60min, B solution was added dropwise ...

Embodiment 3

[0037] S1: Adding solutions A and B: Mix 16 parts of acrylic acid, 23 parts of hydroxyethyl acrylate, 12 parts of hydroxybutyl acrylate, 36 parts of dimethyl maleate, 1.5 parts of mercaptopropionic acid, and 55 parts of deionized water Uniformly used as dripping solution A; mix 1.2 parts of L-ascorbic acid and 89.5 parts of deionized water evenly as dropping solution B, and set aside;

[0038] S2: Add 300 parts of deionized water and 360 parts of EPEG3600 monomer into the reactor, stir at room temperature to fully dissolve, adjust the temperature to 15°C, add 2 parts of acrylic acid to adjust the acidity of the bottom solution, and stir evenly;

[0039]S3: At the initial temperature of 15°C, add 2 parts of 1% ferrous sulfate solution and 2.5 parts of 30% hydrogen peroxide to the mixed solution obtained in step S2, stir for 5 minutes and start adding liquid A and liquid B at a constant speed, and liquid A is added dropwise 50min, B solution was added dropwise for 60min, during ...

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Abstract

The invention discloses a preparation method for synthesizing an ultra-slow-release polycarboxylate superplasticizer from high-activity polyether. The preparation method comprises the following steps:S1, uniformly mixing unsaturated carboxylic acid monomers, unsaturated carboxylic acid monobasic ester, unsaturated carboxylic acid dibasic ester, a chain transfer agent and deionized water to obtaina material A, and uniformly mixing a reducing agent and deionized water to obtain a material B; S2, adding deionized water and a high-activity polyether monomer into a reaction kettle, and carrying out stirring and dissolving at normal temperature; S3, adding an assistant into a solution obtained in the step S2 at 10-20 DEG C, carrying out stirring, starting to dropwise add the material A and thematerial B, and carrying out a curing reaction after the dropwise addition is finished; and S4, adding alkali liquor to adjust a pH value to obtain the ultra-slow-release polycarboxylate superplasticizer. The ultra-slow-release polycarboxylate superplasticizer prepared by the invention has a good slump maintaining function, and can continuously release carboxyl groups with a dispersing function in an alkaline cement paste environment, so a concrete mixture can maintain plasticity for a long time, slump maintaining time can reach more than 3 hours, and the demand for long-distance transportation and construction of concrete is met.

Description

technical field [0001] The invention belongs to the technical field of building material production, and in particular relates to an ultra-slow-release polycarboxylate water reducer and a preparation method thereof. Background technique [0002] As a new type of high-performance water reducer, polycarboxylate water reducer has the advantages of low dosage, high water reducing rate, small slump loss, strong molecular structure adjustability, no chlorine and low alkali, green and environmental protection, etc. Become one of the important components in modern concrete and construction mortar. However, there are still many problems in practical application, especially affected by factors such as cement changes, high-quality sand and gravel mud, long-distance transportation and high-temperature construction, etc., problems such as rapid loss of concrete slump and poor workability have appeared. , Seriously affect the construction and quality of the project. [0003] In order to...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08F283/06C08F220/06C08F220/20C08F222/14C08F220/40C04B24/26C04B103/30
CPCC08F283/065C04B24/2694C04B2103/302
Inventor 徐忠洲
Owner 北京水木佳维新材料技术研究院有限公司
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