Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for preparing concrete water reducer with styrene sulfonate as monomers

A technology of styrene sulfonate and concrete water reducer, which is applied in the field of preparation of concrete water reducer, can solve the problems of limiting application and improving the effect, and achieve the effect of improving application performance

Active Publication Date: 2016-12-07
BEIJING UNIV OF TECH
View PDF6 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the products obtained by the above synthesis methods all have certain deficiencies. From the perspective of molecular structure design and synthesis, researchers have not been able to modify the structure of benzenesulfonyl halides through carboxylic acid-styrenesulfonate copolymers and graft them. The method of polymerizing cationic side chains under the high-valent cerium salt trigger system realizes the composite functional chemical admixture that combines water reduction, slump retention, dispersion, and mud resistance.
The above method of synthesizing a macromonomer only through acylation reaction, or synthesizing a single functional side chain, or introducing a cationic block into the main chain greatly limits its application and improvement effect. It has been proved by facts to synthesize a composite functional group molecular structure with multiple functions. Can significantly improve the application performance of polymers
Therefore, this requires a fundamental innovation in the molecular structure of the synthesized water reducing agent, not sticking to the traditional synthesis method, innovatively using benzenesulfonate to modify benzenesulfonyl halide, and high-valent cerium salt to trigger long chain polycations. , and the synthesis route and characteristics of benzenesulfonyl halide grafted polycation side chains and polyether side chains, which not only have the composite performance of water-reducing and slump-resistant mud, but also are conducive to industrial promotion and application. The domestic work on this aspect There is no report outside

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for preparing concrete water reducer with styrene sulfonate as monomers
  • Method for preparing concrete water reducer with styrene sulfonate as monomers
  • Method for preparing concrete water reducer with styrene sulfonate as monomers

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] First, add 1.43g methacrylic acid, 10.84g itaconic acid, 6.19g sodium p-styrene sulfonate, 14.77g water, 1.23g sodium methacrylate sulfonate, 21.67g mass fraction of 10% peroxide in the reactor Sodium sulfate aqueous solution, and the stirring time between each feeding is 5 minutes, and the temperature is raised to 60 ° C to carry out polymerization reaction, and the reaction is 6.5 hours to obtain the polycarboxylic acid-styrene sulfonate aqueous solution; the obtained polycarboxylic acid-styrene sulfonic acid Vacuumize the brine solution to remove moisture in the system, add 64.61g of dimethylformamide, stir for 12 minutes, add 6.24g of thionyl bromide dropwise to the reactor within 0.7 hours under ice-water bath conditions, and control the temperature at 3°C ​​for constant temperature reaction After 17 hours, 123.49g of methanol was added to wash the precipitate repeatedly 3 times, and the precipitate was vacuum-dried at 80°C to constant weight to obtain polycarboxyli...

Embodiment 2

[0031] After storing the 30% concrete water reducer solution obtained in Example 1 at 6° C. for 30 days, its implementation effect was measured.

Embodiment 3

[0033] First, add 2.87g methacrylic acid, 4.34g itaconic acid, 3.87g maleic acid, 5.15g sodium p-styrene sulfonate, 16.23g water, 0.57g thioglycolic acid, 7.13g mass fraction to the reactor at 20% Ammonium persulfate aqueous solution, and the stirring time between each feeding is 11 minutes, and the temperature is raised to 75°C for polymerization reaction, and the reaction is 4.5 hours to obtain the polycarboxylic acid-styrene sulfonate aqueous solution; the obtained polycarboxylic acid-styrene Sulfonate aqueous solution was vacuumed to remove moisture in the system, 40.57g dimethyl sulfoxide was added, stirred for 14 minutes, 3.57g thionyl chloride was added dropwise to the reactor within 0.6 hours in an ice-water bath, and the temperature was controlled at 4°C to maintain a constant temperature After reacting for 16 hours, add 158.39g of methanol to wash the precipitate repeatedly 5 times, and vacuum-dry the precipitate to constant weight at 65°C to obtain polycarboxylic aci...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a method for preparing a concrete water reducer with styrene sulfonate as monomers, and belongs to the field of water reducers. The method includes the steps that firstly, styrene sulfonate and unsaturated carboxylic acid monomers are subjected to free radical copolymerization to obtain a polycarboxylic acid-styrene sulfonate main chain, and then benzene sulfonate on the main chain is modified into phenylsulfonyl halide groups; then, an oxidation-reduction initiating system is formed by high-valence cerate and alcohol to initiate polymerization of unsaturated cationic quaternary ammonium monomers to obtain a hydroxyl-terminated cationic long chain; then, the polycarboxylic acid main chain containing the phenylsulfonyl halide groups, the hydroxyl-terminated cationic long chain and a polyethylene glycol compound are subjected to sulfonylation to obtain the concrete water reducer. According to the method, based on the molecular structure design principle, by modifying styrene sulfonate into phenylsulfonyl halide and carrying out sulfonylation on grafted cationic side chains and polyethylene glycol side chains, the novel concrete water reducer containing a double-side-chain structure is successfully synthesized; the reaction process is mild, easy to control, capable of saving energy and efficient, and the concrete water reducer shows multiple excellent effects of water reduction for slump loss resistance, clay resistance and the like.

Description

technical field [0001] The invention relates to the technical field of preparing concrete water reducer by using p-styrene sulfonate as a monomer, in particular to a kind of main chain polymerization and then modification using unsaturated carboxylic acid monomer and p-styrene sulfonate A specific preparation method for synthesizing a concrete water reducing agent by polymerizing cationic side chains with benzenesulfonyl halides and then sulfonylation of the main side chains. Background technique [0002] With the continuous development of high-performance concrete technology, the research on high-performance water reducers is also advancing accordingly. The third-generation concrete water reducer with polycarboxylic acid as the main molecular structure - polycarboxylate water reducer, with its With the advantages of low water reducing rate, high water reducing rate, and large degree of freedom in molecular design, it is gradually becoming the most important member of the co...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C08G81/02C08F222/02C08F212/14C08F220/06C08F120/34C08F8/38C08F228/02C04B24/16C04B103/30
CPCC04B24/166C04B2103/302C08F8/38C08F120/34C08F212/14C08F220/06C08F222/02C08G81/025C08F228/02C08F222/06
Inventor 刘晓管佳男王子明彭晶莹崔素萍兰明章
Owner BEIJING UNIV OF TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products