CN113667068A - Glue-reducing type polycarboxylate superplasticizer and preparation method thereof - Google Patents

Glue-reducing type polycarboxylate superplasticizer and preparation method thereof Download PDF

Info

Publication number
CN113667068A
CN113667068A CN202110900522.7A CN202110900522A CN113667068A CN 113667068 A CN113667068 A CN 113667068A CN 202110900522 A CN202110900522 A CN 202110900522A CN 113667068 A CN113667068 A CN 113667068A
Authority
CN
China
Prior art keywords
parts
acid
deionized water
glue
solution
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
Application number
CN202110900522.7A
Other languages
Chinese (zh)
Inventor
乔匡义
周环宇
李雪鸣
王明飞
李崇学
苏高伟
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.)
Cccc Road Construction Transportation Technology Co ltd
Road and Bridge International Co Ltd
Original Assignee
Cccc Road Construction Transportation Technology Co ltd
Road and Bridge International 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 Cccc Road Construction Transportation Technology Co ltd, Road and Bridge International Co Ltd filed Critical Cccc Road Construction Transportation Technology Co ltd
Priority to CN202110900522.7A priority Critical patent/CN113667068A/en
Publication of CN113667068A publication Critical patent/CN113667068A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/06Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polyethers, polyoxymethylenes or polyacetals
    • C08F283/065Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polyethers, polyoxymethylenes or polyacetals on to unsaturated polyethers, polyoxymethylenes or polyacetals
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B24/00Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/24Macromolecular compounds
    • C04B24/26Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C04B24/2688Copolymers containing at least three different monomers
    • C04B24/2694Copolymers containing at least three different monomers containing polyether side chains
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/06Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polyethers, polyoxymethylenes or polyacetals
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/30Water reducers, plasticisers, air-entrainers, flow improvers
    • C04B2103/302Water reducers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Abstract

The invention relates to a glue-reducing polycarboxylic acid water reducing agent and a preparation method thereof, wherein the glue-reducing polycarboxylic acid water reducing agent comprises the following components in parts by weight: 380 parts of prenyl alcohol polyoxyethylene ether macromonomer 340-1500 parts, 46-52 parts of acrylic acid, 3-9 parts of polyoxyethylene-polyoxypropylene segmented copolymer functional monomer, 2-5 parts of thioglycolic acid, 2-6 parts of hydrogen peroxide, 0.5-0.9 part of ascorbic acid and 1500 parts of deionized water 900-1500. The raw materials of the components are mixed according to certain conditions and steps to prepare the water reducing agent with the glue reducing performance, and the water reducing agent can be used as a concrete additive, so that the dosage of cement in the concrete can be greatly reduced on the basis of ensuring various performances of the cement concrete, and the dosage of single cement can be reduced by about 80kg compared with that of the conventional additive by taking C50 concrete as an example.

Description

Glue-reducing type polycarboxylate superplasticizer and preparation method thereof
Technical Field
The invention belongs to the technical field of building materials, relates to a concrete admixture, and particularly relates to a glue-reducing type polycarboxylate superplasticizer and a preparation method thereof.
Background
The current building field is developed rapidly, and the demand of cement concrete is huge. As is well known, the production of cement needs to exploit mineral resources such as limestone, sandstone and the like, is not beneficial to environmental protection, and has prominent contradiction between development and protection. On the premise of ensuring the development, the consumption of the cement concrete is reduced, and the method has great significance for environmental protection.
Disclosure of Invention
The invention aims to provide a concrete admixture, which reduces the using amount of single-component concrete cement on the basis of ensuring various performances of concrete and makes a contribution to solving the contradiction between the development of the current construction industry and the environmental protection.
The polycarboxylate superplasticizer is a common additive in concrete construction. According to the technical specification of concrete admixture application (GB 50119 and 2013), the conventional polycarboxylic acid high-performance water reducing agent is generally divided into a standard type, an early-strength type and a retarding type according to the performance. The polycarboxylic acid has the characteristic of molecular designability, and the characteristic endows the polycarboxylic acid with diversity and derivation of molecular structure, in other words, active large monomers and small monomers with different functions are synthesized according to a certain formula and a certain process, and then the polycarboxylic acid can be polymerized into a polycarboxylic acid product with a certain special function.
According to the characteristics of the polycarboxylic acid, the applicant synthesizes a polycarboxylic acid product with the gel reducing performance by adopting isopentenol polyoxyethylene ether, polyoxyethylene-polyoxypropylene block copolymer, acrylic acid, thioglycolic acid, hydrogen peroxide, ascorbic acid and sodium hydroxide as raw materials and adjusting the proportion and reaction conditions of the raw materials through repeated tests, and the technical scheme is as follows:
the glue-reducing type polycarboxylate superplasticizer is characterized by comprising the following components in parts by weight: 380 parts of prenyl alcohol polyoxyethylene ether macromonomer 340-1500 parts, 46-52 parts of acrylic acid, 3-9 parts of polyoxyethylene-polyoxypropylene segmented copolymer functional monomer, 2-5 parts of thioglycolic acid, 2-6 parts of hydrogen peroxide, 0.5-0.9 part of ascorbic acid and 1500 parts of deionized water 900-1500.
The preparation method of the glue-reducing type polycarboxylate superplasticizer comprises the following steps:
(1) preparing raw materials in parts by weight: 380 parts of isopentenol polyoxyethylene ether macromonomer 340; 46-52 parts of acrylic acid; 3-9 parts of polyoxyethylene-polyoxypropylene segmented copolymer functional monomer; 2-5 parts of thioglycollic acid; 2-6 parts of hydrogen peroxide; 0.5-0.9 part of ascorbic acid; 1500 portions of deionized water were added in 900 portions and divided into 3 equal portions.
(2) Preparing acrylic acid, polyoxyethylene-polyoxypropylene block copolymer and 1 equal part of deionized water into solution A;
(3) preparing mercaptoacetic acid, ascorbic acid and 1 equal part of deionized water into solution B;
(4) heating an isopentenol polyoxyethylene ether macromonomer and 1 equal part of deionized water in a reaction kettle at 40 ℃ until the macromonomer and the deionized water are completely dissolved to prepare solution C;
(5) adding hydrogen peroxide into the solution C, stirring for 5 minutes, and then simultaneously dropwise adding the solution A and the solution B for 3 hours;
(6) after the dropwise addition, the reaction is carried out for 1 hour at the temperature of 40 ℃;
(7) cooling to room temperature, and adding alkali to neutralize to pH 6-7.
The invention can greatly reduce the dosage of cementing materials (the sum of cement and mineral admixtures) in the cement concrete on the basis of ensuring various performances of the cement concrete, takes C50 concrete as an example, the dosage of single cement can be reduced by about 80kg, and the invention has important significance in reducing mineral exploitation and environmental protection.
Detailed Description
The invention provides a glue-reducing polycarboxylic acid water reducing agent which comprises the following components in parts by weight: 380 parts of prenyl alcohol polyoxyethylene ether macromonomer 340-1500 parts, 46-52 parts of acrylic acid, 3-9 parts of polyoxyethylene-polyoxypropylene segmented copolymer functional monomer, 2-5 parts of thioglycolic acid, 2-6 parts of hydrogen peroxide, 0.5-0.9 part of ascorbic acid and 1500 parts of deionized water 900-1500.
The preparation method of the glue-reducing polycarboxylic acid water reducer comprises the following steps:
example 1:
(1) preparing the following raw materials in parts by weight: 340 parts of prenyl alcohol polyoxyethylene ether TPEG2400 macromonomer, 46 parts of acrylic acid, 3 parts of polyoxyethylene-polyoxypropylene block copolymer AP7000 functional monomer, 2 parts of thioglycolic acid, 2 parts of hydrogen peroxide, 0.5 part of ascorbic acid and 900 parts of deionized water.
(2) Preparing a solution A from 46 parts of acrylic acid, 3 parts of a polyoxyethylene-polyoxypropylene block copolymer AP7000 functional monomer and 300 parts of deionized water;
(3) preparing 2 parts of thioglycolic acid, 0.5 part of ascorbic acid and 300 parts of deionized water into solution B;
(4) heating 340 parts of prenyl polyoxyethylene ether TPEG2400 macromonomer and 300 parts of deionized water in a reaction kettle at 40 ℃ until the prenyl polyoxyethylene ether TPEG is completely dissolved to prepare solution C;
(5) adding 2 parts of hydrogen peroxide into the solution C, stirring for 5 minutes, and then simultaneously dropwise adding the solution A and the solution B for 3 hours;
(6) after the dropwise addition, the reaction is carried out for 1 hour at the temperature of 40 ℃;
(7) cooling to room temperature, and adding alkali to neutralize to pH 6-7.
Example 2:
(1) preparing the following raw materials in parts by weight: 360 parts of prenyl alcohol polyoxyethylene ether TPEG2400 macromonomer, 49 parts of acrylic acid, 6 parts of polyoxyethylene-polyoxypropylene block copolymer AP7000 functional monomer, 3.5 parts of thioglycolic acid, 4 parts of hydrogen peroxide, 0.7 part of ascorbic acid and 1200 parts of deionized water.
(2) Preparing 49 parts of acrylic acid, 6 parts of polyoxyethylene-polyoxypropylene segmented copolymer AP7000 and 400 parts of deionized water into solution A;
(3) preparing solution B from 3.5 parts of thioglycolic acid, 0.7 part of ascorbic acid and 400 parts of deionized water;
(4) heating 360 parts of prenyl polyoxyethylene ether TPEG2400 macromonomer and 400 parts of deionized water in a reaction kettle at 40 ℃ until the monomers are completely dissolved to prepare solution C;
(5) adding 4 parts of hydrogen peroxide into the solution C, stirring for 5 minutes, and then simultaneously dropwise adding the solution A and the solution B for 3 hours;
(6) after the dropwise addition, the reaction is carried out for 1 hour at the temperature of 40 ℃;
(7) cooling to room temperature, and adding alkali to neutralize to pH 6-7.
Example 3:
(1) preparing the following raw materials in parts by weight: 380 parts of prenyl alcohol polyoxyethylene ether TPEG2400 macromonomer, 52 parts of acrylic acid, 9 parts of polyoxyethylene-polyoxypropylene block copolymer AP7000 functional monomer, 5 parts of thioglycolic acid, 6 parts of hydrogen peroxide, 0.9 part of ascorbic acid and 1500 parts of deionized water.
(2) Preparing 52 parts of acrylic acid, 9 parts of polyoxyethylene-polyoxypropylene segmented copolymer AP7000 and 500 parts of deionized water into solution A;
(3) preparing 5 parts of thioglycolic acid, 0.9 part of ascorbic acid and 500 parts of deionized water into solution B;
(4) heating 380 parts of prenyl polyoxyethylene ether TPEG2400 macromonomer and 500 parts of deionized water in a reaction kettle at 40 ℃ until the prenyl polyoxyethylene ether TPEG is completely dissolved to prepare solution C;
(5) adding 5 parts of hydrogen peroxide into the solution C, stirring for 5 minutes, and then simultaneously dropwise adding the solution A and the solution B for 3 hours;
(6) after the dropwise addition, the reaction is carried out for 1 hour at the temperature of 40 ℃;
(7) cooling to room temperature, and adding alkali to neutralize to pH 6-7.
The glue-reducing polycarboxylic acid water reducing agent prepared by the embodiment is used as a concrete admixture, taking C50 cement concrete as an example, and comprises the following components in parts by weight:
cement (p.o42.5), sand: the gravel with the particle size of 5-10mm, the gravel with the particle size of 10-20mm, water and the glue-reducing polycarboxylic acid water reducing agent are 400:826:438:657:128: 4.8.
The main performance indexes of the concrete are compared with the test results of the commonly used concrete admixture (Kejie) sold in the market at present
Table 1:
Figure BDA0003199620230000041
TABLE 1 concrete test results
It can be seen that the working performance of the C50 concrete mixture using the admixture and the mechanical property of the hardened concrete are superior to those of the conventional product (Kejie), and the 7-day compressive strength is 23.1-25.5 MPa higher than the Kejie. According to the conventional single cement dosage of C50 concrete 480Kg, the single cement dosage of the invention is 400Kg, and each side of C50 concrete can save cement 80 Kg.

Claims (5)

1. The glue-reducing type polycarboxylate superplasticizer is characterized by comprising the following components in parts by weight: 380 parts of prenyl alcohol polyoxyethylene ether macromonomer 340-1500 parts, 46-52 parts of acrylic acid, 3-9 parts of polyoxyethylene-polyoxypropylene segmented copolymer functional monomer, 2-5 parts of thioglycolic acid, 2-6 parts of hydrogen peroxide, 0.5-0.9 part of ascorbic acid and 1500 parts of deionized water 900-1500.
2. The glue-reducing type polycarboxylate superplasticizer according to claim 1, characterized by comprising the following components in parts by weight: 340 parts of prenyl alcohol polyoxyethylene ether macromonomer, 46 parts of acrylic acid, 3 parts of polyoxyethylene-polyoxypropylene segmented copolymer functional monomer, 2 parts of thioglycollic acid, 2 parts of hydrogen peroxide, 0.5 part of ascorbic acid and 900 parts of deionized water.
3. The glue-reducing type polycarboxylate superplasticizer according to claim 1, characterized by comprising the following components in parts by weight: 360 parts of prenyl alcohol polyoxyethylene ether macromonomer, 49 parts of acrylic acid, 6 parts of polyoxyethylene-polyoxypropylene segmented copolymer functional monomer, 3.5 parts of thioglycollic acid, 4 parts of hydrogen peroxide, 0.7 part of ascorbic acid and 1200 parts of deionized water.
4. The glue-reducing type polycarboxylate superplasticizer according to claim 1, characterized by comprising the following components in parts by weight: 380 parts of prenyl alcohol polyoxyethylene ether macromonomer, 52 parts of acrylic acid, 9 parts of polyoxyethylene-polyoxypropylene block copolymer functional monomer, 5 parts of thioglycollic acid, 6 parts of hydrogen peroxide, 0.9 part of ascorbic acid and 1500 parts of deionized water.
5. The preparation method of the glue-reducing type polycarboxylate superplasticizer according to claim 1 is characterized by comprising the following steps:
(1) preparing raw materials in parts by weight: 380 parts of isopentenol polyoxyethylene ether macromonomer 340; 46-52 parts of acrylic acid; 3-9 parts of polyoxyethylene-polyoxypropylene segmented copolymer functional monomer; 2-5 parts of thioglycollic acid; 2-6 parts of hydrogen peroxide; 0.5-0.9 part of ascorbic acid; 1500 portions of deionized water were added in 900 portions and divided into 3 equal portions.
(2) Preparing acrylic acid, polyoxyethylene-polyoxypropylene block copolymer and 1 equal part of deionized water into solution A;
(3) preparing mercaptoacetic acid, ascorbic acid and 1 equal part of deionized water into solution B;
(4) heating an isopentenol polyoxyethylene ether macromonomer and 1 equal part of deionized water in a reaction kettle at 40 ℃ until the macromonomer and the deionized water are completely dissolved to prepare solution C;
(5) adding hydrogen peroxide into the solution C, stirring for 5 minutes, and then simultaneously dropwise adding the solution A and the solution B for 3 hours;
(6) after the dropwise addition, the reaction is carried out for 1 hour at the temperature of 40 ℃;
(7) cooling to room temperature, and adding alkali to neutralize to pH 6-7.
CN202110900522.7A 2021-08-06 2021-08-06 Glue-reducing type polycarboxylate superplasticizer and preparation method thereof Pending CN113667068A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110900522.7A CN113667068A (en) 2021-08-06 2021-08-06 Glue-reducing type polycarboxylate superplasticizer and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110900522.7A CN113667068A (en) 2021-08-06 2021-08-06 Glue-reducing type polycarboxylate superplasticizer and preparation method thereof

Publications (1)

Publication Number Publication Date
CN113667068A true CN113667068A (en) 2021-11-19

Family

ID=78541676

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110900522.7A Pending CN113667068A (en) 2021-08-06 2021-08-06 Glue-reducing type polycarboxylate superplasticizer and preparation method thereof

Country Status (1)

Country Link
CN (1) CN113667068A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114573766A (en) * 2022-03-28 2022-06-03 湖南凝英新材料科技有限公司 Preparation method of glue-reducing concrete water reducing agent and water reducing agent
CN116751017A (en) * 2023-08-10 2023-09-15 中交路桥建设有限公司 Glue-reducing water-reducing concrete and production system thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104016614A (en) * 2014-06-13 2014-09-03 石家庄市长安育才建材有限公司 Polycarboxylate water reducer with defoaming function and preparation method of water reducer
CN104692699A (en) * 2015-02-05 2015-06-10 石家庄市长安育才建材有限公司 Early strength type ether polycarboxylate superplasticizer and preparation method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104016614A (en) * 2014-06-13 2014-09-03 石家庄市长安育才建材有限公司 Polycarboxylate water reducer with defoaming function and preparation method of water reducer
CN104692699A (en) * 2015-02-05 2015-06-10 石家庄市长安育才建材有限公司 Early strength type ether polycarboxylate superplasticizer and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114573766A (en) * 2022-03-28 2022-06-03 湖南凝英新材料科技有限公司 Preparation method of glue-reducing concrete water reducing agent and water reducing agent
CN116751017A (en) * 2023-08-10 2023-09-15 中交路桥建设有限公司 Glue-reducing water-reducing concrete and production system thereof
CN116751017B (en) * 2023-08-10 2023-11-24 中交路桥建设有限公司 Glue-reducing water-reducing concrete and production system thereof

Similar Documents

Publication Publication Date Title
CN108659177B (en) High-adaptability ultra-long slow-release slump retaining agent and preparation method thereof at normal and low temperature
CN109400821B (en) Concrete bleeding-resistant inhibitor with water reducing function and preparation method thereof
CN110642993B (en) Preparation method of retarding ether polycarboxylate superplasticizer
CN109337024B (en) Preparation method of retarding polycarboxylate superplasticizer
CN113667068A (en) Glue-reducing type polycarboxylate superplasticizer and preparation method thereof
CN111777722A (en) Anti-mud slump-retaining polycarboxylate superplasticizer and preparation method thereof
CN112961290A (en) Anti-mud polycarboxylic acid slump retaining water reducer and preparation method thereof
CN108821640B (en) Concrete mortar anti-cracking additive and preparation method thereof
CN109650762B (en) Phosphate type polycarboxylate superplasticizer and preparation method thereof
CN113698550B (en) Gradient slow-release type polycarboxylate superplasticizer and preparation method and application thereof
CN110643003B (en) Preparation method of retarding type ester polycarboxylate superplasticizer
CN113149507A (en) Preparation method of comprehensive slump-retaining polycarboxylate superplasticizer
CN117126346A (en) Nuclear early-strength polycarboxylate superplasticizer and preparation method thereof
CN112521099A (en) Production process of quick-setting concrete
CN111019064A (en) Polycarboxylate superplasticizer and preparation method thereof
CN113307539B (en) Compound polycarboxylate superplasticizer and preparation method thereof
CN107759122B (en) Concrete glue reducing agent
CN113429134B (en) Method for adjusting fluidity and setting time of chemically-activated cementing material system
CN113929366B (en) Recycled concrete with high slump retaining performance and preparation method thereof
CN111620594B (en) Polycarboxylate superplasticizer and preparation method thereof
CN114133492A (en) Preparation method of polycarboxylic acid concrete water reducing agent
CN109535347B (en) Preparation method of block water-retaining concrete admixture
CN109111556B (en) Ester ether crosslinking polycarboxylic acid workability regulator and preparation method thereof
CN112142924A (en) Preparation method of early-strength polycarboxylic acid high-performance water reducing agent
CN114369208B (en) Preparation method and application of mud-resistant high-adsorption water-reducing polycarboxylate superplasticizer

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination