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CN111454014B - Mortar and concrete shrinkage reducing agent containing organic silicon and preparation method thereof - Google Patents

Mortar and concrete shrinkage reducing agent containing organic silicon and preparation method thereof Download PDF

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CN111454014B
CN111454014B CN202010254259.4A CN202010254259A CN111454014B CN 111454014 B CN111454014 B CN 111454014B CN 202010254259 A CN202010254259 A CN 202010254259A CN 111454014 B CN111454014 B CN 111454014B
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reducing agent
mixture
mortar
concrete
organic silicon
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CN111454014A (en
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康净鑫
黄永毅
陈吓敏
李芳�
肖招营
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Xiamen Road & Bridge Sunstone Buidling Material Technology Co ltd
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    • 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
    • C04B40/00Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
    • C04B40/0028Aspects relating to the mixing step of the mortar preparation
    • C04B40/0039Premixtures of ingredients
    • C04B40/0046Premixtures of ingredients characterised by their processing, e.g. sequence of mixing the ingredients when preparing the premixtures

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  • Organic Chemistry (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

The invention discloses a mortar and concrete shrinkage reducing agent containing organosilicon and a preparation method thereof, wherein the mortar and concrete shrinkage reducing agent has a pH value of 5.5-6 and is prepared from the following raw materials: TPEG, unsaturated carboxylic acid and derivatives thereof, anionic surfactant, organosilicon monomer, ethylene glycol acrylate hydrophobic monomer, initiator, reducing agent, chain transfer agent, liquid alkali and deionized water. The TPEG, specific unsaturated carboxylic acid and derivatives thereof, specific organic silicon monomers and specific glycol acrylate hydrophobic monomers are used as basic raw materials, molecular structure design and regulation are carried out according to the functional requirements of shrinkage reduction and dispersion performance, unsaturated polyether and unsaturated carboxylic acid are copolymerized to form a main chain, amino, sulfonic acid groups, amide groups, siloxane structural monomers, glycol acrylate monomers and the like are introduced into the molecular structure of the polymer, and the drying shrinkage rate of cement mortar can be effectively reduced.

Description

Mortar and concrete shrinkage reducing agent containing organic silicon and preparation method thereof
Technical Field
The invention belongs to the technical field of concrete admixtures, and particularly relates to mortar and concrete shrinkage reducing agent containing organic silicon and a preparation method thereof.
Background
Cracks or crazes caused by the shrinkage of concrete affect the appearance of buildings, reduce the service life of concrete, and even cause serious problems in the safety of concrete structures. The problem of shrinkage cracking of concrete, especially high-performance concrete, has attracted great attention in the engineering industry, and although the shrinkage of concrete is reduced to a certain extent by polycarboxylic acid water reducing agent, the requirements of engineering are still difficult to meet.
At present, the early shrinkage cracking of concrete is mainly controlled or reduced by the following measures: (1) the shrinkage is reduced by comprehensively optimizing the matching ratio; (2) the shrinkage reducing agent, the fiber or the expanding agent are blended to improve the plastic shrinkage crack resistance of the concrete or compensate the plastic shrinkage of the concrete; (3) the plastic shrinkage is reduced by spraying a surface curing agent or early wet curing to reduce the evaporation rate of water on the surface of the concrete.
The concrete shrinkage reducing agent is mainly used for reducing the shrinkage of concrete by reducing the surface tension of water in concrete pores and reducing the shrinkage force in the water evaporation process so as to achieve the purpose of reducing concrete cracks. In China, no shaped concrete shrinkage-reducing agent product is sold, and foreign products are difficult to buy. As with other admixtures, each manufacturer is kept confidential with respect to the specific components of its shrinkage-reducing agent.
Therefore, the development of shrinkage reducing agent products capable of effectively reducing the shrinkage of concrete has important significance for improving the volume stability of concrete and improving the durability of concrete structures.
Disclosure of Invention
The invention aims to overcome the defects of the prior art and provide the mortar and concrete shrinkage reducing agent containing the organic silicon.
The invention also aims to provide a preparation method of the mortar and concrete shrinkage reducing agent containing the organic silicon.
The technical scheme of the invention is as follows:
a mortar and concrete shrinkage reducing agent containing organic silicon is characterized in that: the pH value is 5.5-6, and the medicine is prepared from the following raw materials in parts by weight:
Figure GDA0003339903080000011
Figure GDA0003339903080000021
the structural formula of the TPEG is CH2=C(CH3)CH2CH2O(CH2CH2O)nH, wherein n is a positive integer;
the unsaturated carboxylic acid and its derivative comprises at least one of acrylic acid, acrylamide, methacrylic acid, maleic anhydride, methyl acrylate, and dimethyl maleate;
the organic silicon monomer comprises at least one of vinyltrimethylsilane, trifluoromethyltrimethylsilane, vinyltriethoxysilane and gamma-methacryloxypropyltrimethoxysilane;
the ethylene glycol acrylate hydrophobic monomer comprises at least one of polyethylene glycol dimethacrylate, polyethylene glycol acrylate, diethylene glycol monoacrylate and ethylene glycol dimethacrylate.
The TPEG, specific unsaturated carboxylic acid and derivatives thereof, specific organic silicon monomers and specific glycol acrylate hydrophobic monomers are used as basic raw materials, molecular structure design and regulation are carried out according to the functional requirements of shrinkage reduction and dispersion performance, unsaturated polyether and unsaturated carboxylic acid are copolymerized to form a main chain, amino, sulfonic acid groups, amide groups, siloxane structural monomers, glycol acrylate monomers and the like are introduced into the molecular structure of the polymer, and the drying shrinkage rate of cement mortar can be effectively reduced.
According to the invention, a certain amount of sulfonic acid groups are grafted to enhance the adsorption performance and charge adsorption capacity of the water reducing agent and the surface of concrete particles, so that the fluidity and the workability of concrete are improved. The amido is an amphoteric group, so that the sensitivity of the polyether to inorganic salt ions can be reduced, the polyether keeps an extended conformation, and the polyether can better play a dispersing role.
According to the invention, by introducing the amino functional group, the shrinkage reducing agent is more easily combined with water molecules to form a layer of water film, and the amino group has positive charges, and the shrinkage reducing molecules adsorbed on the surface of cement particles are more easily dispersed due to the repulsion of like charges.
The hydrophobic monomers such as ethylene glycol acrylate monomers and organic silicon monomers added in the invention can effectively reduce the surface tension of the solution, thereby reducing the drying shrinkage of the concrete. Furthermore, a water-retaining group with a siloxane structure is introduced, a micro-cross-linked structure can be formed, the viscosity of pore water in the concrete is increased, the adsorption effect of water in concrete colloid is enhanced, and the shrinkage of the concrete can be further reduced.
The shrinkage reducing agent and the water reducing agent are mixed together, so that the water reducing rate of mortar and concrete can be increased properly, and the synergistic effect is achieved.
The preparation method of the mortar and concrete shrinkage reducing agent containing the organic silicon comprises the following steps:
(1) TPEG, anionic surfactant and a proper amount of deionized water are uniformly mixed to obtain a first mixture; mixing unsaturated carboxylic acid and derivatives thereof, an organic silicon monomer, a glycol acrylate hydrophobic monomer and a proper amount of deionized water to obtain a second mixture; mixing a reducing agent, a chain transfer agent and a proper amount of deionized water to obtain a third mixture;
(2) placing the first mixture into a reaction kettle, heating to 37-43 ℃ while continuously stirring, adding an initiator once after the temperature is kept stable, dropwise adding the second mixture and the third mixture within 1-4h, and reacting at 37-43 ℃ for 1-2 h;
(3) and (3) adding liquid alkali into the material obtained in the step (2) to obtain the mortar containing the organic silicon and the concrete shrinkage reducing agent.
The preparation method of the invention adopts normal pressure production, has low equipment requirement and convenient operation, is beneficial to industrial production, does not contain chloride ions in the product, and has no corrosion hazard to reinforcing steel bars in concrete.
Drawings
FIG. 1 is a graph showing the change in concrete shrinkage at different loadings in a comparative test of the present invention.
Detailed Description
The technical solution of the present invention will be further illustrated and described below with reference to the accompanying drawings by means of specific embodiments.
In a preferred embodiment of the present invention, the unsaturated carboxylic acid and its derivative is at least one of acrylic acid, acrylamide, methacrylic acid, maleic anhydride, methyl acrylate, and dimethyl maleate.
In a preferred embodiment of the present invention, the silicone monomer is at least one of vinyltrimethylsilane, trifluoromethyltrimethylsilane, vinyltriethoxysilane, and gamma-methacryloxypropyltrimethoxysilane.
In a preferred embodiment of the present invention, the glycol acrylate hydrophobic monomer is at least one of polyethylene glycol dimethacrylate, polyethylene glycol acrylate, diethylene glycol monoacrylate and ethylene glycol dimethacrylate.
In a preferred embodiment of the present invention, the anionic surfactant comprises at least one of sodium dodecyl sulfonate, sodium dodecyl benzene sulfonate, sodium polystyrene sulfonate, and sodium methallyl sulfonate.
In a preferred embodiment of the present invention, the reducing agent includes at least one of sodium bisulfite, vitamin C, ferrous sulfate, and glucose.
In a preferred embodiment of the present invention, the initiator includes at least one of ammonium persulfate and potassium persulfate.
In a preferred embodiment of the present invention, the chain transfer agent comprises at least one of thioglycolic acid, 2-mercaptopropionic acid, 3-mercaptopropionic acid, and sodium methallylsulfonate.
In a preferred embodiment of the present invention, the solute in the liquid caustic soda comprises at least one of potassium hydroxide and sodium hydroxide.
Example 1
(1) 50g of TPEG (number average molecular weight of 2300-3) 10g of sodium dodecyl sulfate, deionized water and a proper amount of deionized water are uniformly mixed to obtain a first mixture; mixing 15g of acrylic acid, 10g of acrylamide, 1.2g of vinyltrimethoxysilane, 1.2g of ethylene glycol dimethacrylate and a proper amount of deionized water to obtain a second mixture; mixing 0.8g of vitamin C, 0.8g of thioglycolic acid and a proper amount of deionized water to obtain a third mixture;
(2) placing the first mixture into a reaction kettle, heating to 37-43 ℃ while continuously stirring, adding 1.2g of ammonium persulfate once after the temperature is kept stable, dropwise adding the second mixture and the third mixture within 1-4h, and reacting at 37-43 ℃ for 1-2h in a heat preservation way after dropwise adding;
(3) and (3) adding liquid caustic soda into the material obtained in the step (2), and adjusting the pH value to 5.5-6 to obtain the mortar containing the organic silicon and the concrete shrinkage reducing agent JS-1.
Example 2
(1) 50g of TPEG (number average molecular weight of 2300-3) 8g of sodium dodecyl benzene sulfonate and a proper amount of deionized water are uniformly mixed to obtain a first mixture; mixing 20g of methacrylic acid, 10g of acrylamide, 1.0g of vinyltriethoxysilane, 1.5g of polyethylene glycol acrylate and a proper amount of deionized water to obtain a second mixture; mixing 0.9g of vitamin C, 1.0g of 2-mercaptopropionic acid and a proper amount of deionized water to obtain a third mixture;
(2) placing the first mixture into a reaction kettle, heating to 37-43 ℃ while continuously stirring, adding 1.0g of potassium persulfate once after the temperature is kept stable, dropwise adding the second mixture and the third mixture within 1-4h, and keeping the temperature at 37-43 ℃ for 1-2h after dropwise adding;
(3) and (3) adding liquid caustic soda into the material obtained in the step (2), and adjusting the pH value to 5.5-6 to obtain the mortar containing the organic silicon and the concrete shrinkage reducing agent JS-2.
Example 3
(1) 50g of TPEG (number average molecular weight of 2300-3) Uniformly mixing 8g of sodium methallyl sulfonate and a proper amount of deionized water to obtain a first mixture; mixing 16g of acrylic acid, 10g of acrylamide, 0.8g of gamma-methacryloxypropyltrimethoxysilane, 1.2g of polyethylene glycol dimethacrylate and a proper amount of deionized water to obtain a second mixture; mixing 0.6g of sodium bisulfite, 0.8g of 2-mercaptopropionic acid, and an appropriate amount of deionized water to obtain a third mixture;
(2) placing the first mixture into a reaction kettle, heating to 37-43 ℃ while continuously stirring, adding 1.6g of ammonium persulfate once after the temperature is kept stable, dropwise adding the second mixture and the third mixture within 1-4h, and reacting at 37-43 ℃ for 1-2h in a heat preservation way after dropwise adding;
(3) and (3) adding liquid caustic soda into the material obtained in the step (2), and adjusting the pH value to 5.5-6 to obtain the mortar containing the organic silicon and the concrete shrinkage reducing agent JS-3.
Example 4
(1) 50g of TPEG (number average molecular weight of 2300-3) Uniformly mixing 10g of sodium polystyrene sulfonate and a proper amount of deionized water to obtain a first mixture; mixing 20g of acrylic acid, 10g of acrylamide, 1.4g of trifluoromethyltriethylsilane, 1.6g of ethylene glycol dimethacrylate and a proper amount of deionized water to obtain a second mixture; mixing 1g of vitamin C, 0.8g of 3-mercaptopropionic acid and a proper amount of deionized water to obtain a third mixture;
(2) placing the first mixture into a reaction kettle, heating to 37-43 ℃ while continuously stirring, adding 1.2g of ammonium persulfate once after the temperature is kept stable, dropwise adding the second mixture and the third mixture within 1-4h, and reacting at 37-43 ℃ for 1-2h in a heat preservation way after dropwise adding;
(3) and (3) adding liquid caustic soda into the material obtained in the step (2), and adjusting the pH value to 5.5-6 to obtain the mortar containing the organic silicon and the concrete shrinkage reducing agent JS-4.
Example 5
(1) 50g of TPEG (number average molecular weight of 2300-3) Uniformly mixing 10g of sodium methallyl sulfonate and a proper amount of deionized water to obtain a first mixture; mixing 18g of acrylic acid, 10g of acrylamide, 1.4g of vinyltrimethoxysilane, 1.0g of polyethylene glycol dimethacrylate and a suitable amount of deionized water to obtain a second mixture; mixing 0.8g of sodium bisulfite, 0.6g of thioglycolic acid and a suitable amount of deionized water to obtain a third mixture;
(2) placing the first mixture into a reaction kettle, heating to 37-43 ℃ while continuously stirring, adding 1.2g of ammonium persulfate once after the temperature is kept stable, dropwise adding the second mixture and the third mixture within 1-4h, and reacting at 37-43 ℃ for 1-2h in a heat preservation way after dropwise adding;
(3) and (3) adding liquid caustic soda into the material obtained in the step (2), and adjusting the pH value to 5.5-6 to obtain the mortar containing the organic silicon and the concrete shrinkage reducing agent JS-5.
Example 6
(1) 30g of TPEG (number average molecular weight of 2300-3) Uniformly mixing 10g of sodium polystyrene sulfonate and a proper amount of deionized water to obtain a first mixture; mixing 18g of methacrylic acid, 5g of maleic anhydride, 5g of acrylamide, 1.0g of trifluoromethyltrimethoxysilane, 0.8g of ethylene glycol dimethacrylate and a proper amount of deionized water to obtain a second mixture; mixing 0.8g of vitamin C, 0.6g of thioglycolic acid and a proper amount of deionized water to obtain a third mixture;
(2) placing the first mixture into a reaction kettle, heating to 37-43 ℃ while continuously stirring, adding 1.0g of potassium persulfate once after the temperature is kept stable, dropwise adding the second mixture and the third mixture within 1-4h, and keeping the temperature at 37-43 ℃ for 1-2h after dropwise adding;
(3) and (3) adding liquid caustic soda into the material obtained in the step (2), and adjusting the pH value to 5.5-6 to obtain the mortar containing the organic silicon and the concrete shrinkage reducing agent JS-6.
Example 7
(1) 30g of TPEG (number average molecular weight of 2300-3) Uniformly mixing 8g of sodium methallyl sulfonate and a proper amount of deionized water to obtain a first mixture; mixing 18g of acrylic acid, 5g of dimethyl maleate, 5g of acrylamide, 1.2g of vinyltrimethoxysilane, 1.0g of polyethylene glycol dimethacrylate and a suitable amount of deionized water to obtain a second mixture; mixing 0.8g of sodium bisulfite, 0.6g of 2-mercaptopropionic acid, and an appropriate amount of deionized water to obtain a third mixture;
(2) placing the first mixture into a reaction kettle, heating to 37-43 ℃ while continuously stirring, adding 1.2g of ammonium persulfate once after the temperature is kept stable, dropwise adding the second mixture and the third mixture within 1-4h, and reacting at 37-43 ℃ for 1-2h in a heat preservation way after dropwise adding;
(3) and (3) adding liquid caustic soda into the material obtained in the step (2), and adjusting the pH value to 5.5-6 to obtain the mortar containing the organic silicon and the concrete shrinkage reducing agent JS-7.
Example 8
(1) 50g of TPEG (a), (b), (c), (d) and (d)The number average molecular weight is 2300-3) 8g of sodium polystyrene sulfonate and a proper amount of deionized water are uniformly mixed to obtain a first mixture; mixing 15g of acrylic acid, 5g of methyl acrylate, 10g of acrylamide, 1.3g of gamma-methacryloxypropyltrimethoxysilane, 1.0g of diethylene glycol monoacrylate and a proper amount of deionized water to obtain a second mixture; mixing 0.8g of sodium bisulfite, 0.6g of 3-mercaptopropionic acid, and an appropriate amount of deionized water to obtain a third mixture;
(2) placing the first mixture into a reaction kettle, heating to 37-43 ℃ while continuously stirring, adding 1.2g of ammonium persulfate once after the temperature is kept stable, dropwise adding the second mixture and the third mixture within 1-4h, and reacting at 37-43 ℃ for 1-2h in a heat preservation way after dropwise adding;
(3) and (3) adding liquid caustic soda into the material obtained in the step (2), and adjusting the pH value to 5.5-6 to obtain the mortar containing the organic silicon and the concrete shrinkage reducing agent JS-8.
Comparative test
1. Drying shrinkage test of cement mortar
According to the regulation in JC/T603-2004, the mixing ratio of cement and sand is kept unchanged in a cement mortar drying shrinkage test, the mass ratio of the cement of cement mortar to standard sand is 1: 2, the cement used in the test is the reference cement, the sand is the standard sand, and the water consumption of the mortar is determined according to the fluidity of the prepared mortar reaching 130 mm-140 mm. Placing the prepared mortar into a curing box or fog room with the temperature of 20 +/-1 ℃ and the relative humidity of not less than 90 percent, curing for 24 +/-2 hours, demolding, then placing into water for curing for 2 days, taking out and measuring the initial length L0, and then placing into a drying curing room with the temperature of 20 +/-3 ℃ and the relative humidity of 50 +/-4 percent. From the molding day, the length of the product is measured as L7 at 7d, the length of the product is measured as L28 at 28d, a certain shrinkage reducing agent product sold in the comparative example 1 is selected, and experimental water is used in the comparative example 2. The test results are shown in table 1:
table 1 cement mortar dry shrinkage test results for different embodiments
Figure GDA0003339903080000071
Note:
in table 1, the data before "/" indicates the drying shrinkage of cement mortar, and the data after "/" indicates the shrinkage ratio to comparative example 2.
As can be seen from the data in Table 1, the drying shrinkage of the cement mortar can be effectively reduced, the drying shrinkage of the cement mortar of 7d is reduced by about 10% compared with that of comparative example 2, the drying shrinkage of the cement mortar of 28d is reduced by about 20% compared with that of comparative example 2, and the cement mortar has no adverse effect on the strength of the cement mortar of 28 d.
2. Drying shrinkage test of concrete
The slump of the fresh concrete is kept at 200 +/-10 mm by adjusting the mixing amount of the water reducing agent, the mixing proportion of the concrete is shown in table 2, and the test result is shown in table 3.
TABLE 2 concrete mix proportions
Figure GDA0003339903080000081
TABLE 3 variation of concrete shrinkage for different embodiments
Sample (I) Mixing amount/% 7d dry shrinkage/x 10-6 28d dry shrinkage/x 10-6
Comparative example 1 0.2 -98 -178
Comparative example 2 0.2 -105 -190
JS-1 0.2 -86 -167
JS-2 0.2 -79 -161
JS-3 0.2 -84 -158
JS-4 0.2 -75 -143
JS-5 0.2 -81 -151
JS-6 0.2 -73 -159
JS-7 0.2 -77 -148
JS-8 0.2 -82 -154
From the test results in table 3, it can be seen that the concrete performance test using the raw materials and the mixing ratio shown in table 2 according to the present invention can effectively reduce the drying shrinkage of concrete by up to 28.6% at age 7 days and by up to 24.7% at age 28 days, compared to comparative example 2.
Further, a better sample is selected, concrete performance tests of different doping amount shrinkage reducing agent products are carried out, the doping amount of the water reducing agent is adjusted to keep the slump of fresh concrete within 200 +/-10 mm, the concrete mixing ratio is shown in a table 4, the test result is shown in a table 5, and the visual chart is shown in a figure 1.
TABLE 4 concrete mix proportions
Figure GDA0003339903080000091
TABLE 5 variation of the invention in the dry shrinkage of the concrete at different loadings
Sample (I) Mixing amount/% 1d dry shrinkage/x 10-6 3d dry shrinkage/x 10-6 7d dry shrinkage/x 10-6 28d dry shrinkage/x 10-6
Comparative example 2 0.2 -68.3 -205.7 -377.3 -672
JS-4 0.2 -41.7 -140.7 -259.3 -463.7
JS-4 0.15 -49 -167 -301.3 -510
JS04 0.25 -40.3 -135.7 -241.7 -434.3
From the data in table 5 and fig. 1, it can be seen that the present invention can effectively reduce the dry shrinkage of concrete in the concrete performance test using the raw materials and the mixing ratio shown in table 4, and the shrinkage reducing ability is further improved as the mixing amount of the present invention is increased. Compared with comparative example 2, the addition amount of the additive is 0.25%, the addition amount can be reduced by 35.9% when the age is 7 days, and the addition amount can be reduced by 35.4% at the highest when the age is 28 days.
Experimental results show that the invention achieves the purpose of reduction.
The above description is only a preferred embodiment of the present invention, and therefore should not be taken as limiting the scope of the invention, which is defined by the appended claims.

Claims (4)

1. A mortar and concrete shrinkage reducing agent containing organic silicon is characterized in that: the pH =5.5-6, and is prepared from the following raw materials in parts by weight:
the number average molecular weight is 2300-3TPEG (1) 100 parts by weight
50-60 parts by weight of unsaturated carboxylic acid and derivative thereof
5-10 parts by weight of anionic surfactant
1-2 parts of organosilicon monomer
1-5 parts of glycol acrylate hydrophobic monomer
0.3 to 0.6 portion of initiator
0.2 to 0.4 portion of reducing agent
0.2-0.5 weight part of chain transfer agent
Proper amount of liquid caustic soda
Proper amount of deionized water
The structural formula of the TPEG is CH2= C (CH3)CH2CH2O(CH2CH2O)nH, wherein n is a positive integer;
the unsaturated carboxylic acid and the derivative thereof are at least one of acrylic acid, acrylamide, methacrylic acid, maleic anhydride, methyl acrylate and dimethyl maleate; the organic silicon monomer is at least one of vinyltrimethylsilane, trifluoromethyltrimethylsilane, vinyltriethoxysilane and gamma-methacryloxypropyltrimethoxysilane; the ethylene glycol acrylate hydrophobic monomer is at least one of polyethylene glycol dimethacrylate, polyethylene glycol acrylate, diethylene glycol monoacrylate and ethylene glycol dimethacrylate; the anionic surfactant comprises at least one of sodium dodecyl sulfonate, sodium dodecyl benzene sulfonate, sodium polystyrene sulfonate and sodium methyl propylene sulfonate; the reducing agent comprises at least one of sodium bisulfite, vitamin C, ferrous sulfate and glucose;
the preparation method comprises the following steps:
(1) TPEG, anionic surfactant and a proper amount of deionized water are uniformly mixed to obtain a first mixture; mixing unsaturated carboxylic acid and derivatives thereof, an organic silicon monomer, a glycol acrylate hydrophobic monomer and a proper amount of deionized water to obtain a second mixture; mixing a reducing agent, a chain transfer agent and a proper amount of deionized water to obtain a third mixture;
(2) placing the first mixture into a reaction kettle, heating to 37-43 ℃ while continuously stirring, adding an initiator once after the temperature is kept stable, dropwise adding the second mixture and the third mixture within 1-4h, and reacting at 37-43 ℃ for 1-2 h;
(3) and (3) adding liquid alkali into the material obtained in the step (2) to obtain the mortar containing the organic silicon and the concrete shrinkage reducing agent.
2. The silicone-containing mortar and concrete shrinkage reducing agent of claim 1, wherein: the initiator comprises at least one of ammonium persulfate and potassium persulfate.
3. The silicone-containing mortar and concrete shrinkage reducing agent of claim 1, wherein: the chain transfer agent comprises at least one of thioglycolic acid, 2-mercaptopropionic acid, 3-mercaptopropionic acid and sodium methallylsulfonate.
4. The silicone-containing mortar and concrete shrinkage reducing agent of claim 1, wherein: the solute in the liquid alkali comprises at least one of potassium hydroxide and sodium hydroxide.
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Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103333297A (en) * 2013-06-24 2013-10-02 北京工业大学 Preparation method of reduced polycarboxylate-type high-performance water reducing agent
CN104592460A (en) * 2015-01-28 2015-05-06 南京瑞迪高新技术有限公司 Preparation method of reduction type polycarboxylate superplasticizer
CN104628972A (en) * 2015-01-30 2015-05-20 江苏奥莱特新材料有限公司 Preparation method of anti-crack shrinkage reducing polycarboxylate based superplasticizer
CN105601152A (en) * 2015-12-17 2016-05-25 江苏苏博特新材料股份有限公司 Efficient shrinkage-reducing anti-cracking agent and preparation method thereof
CN106084147A (en) * 2016-06-04 2016-11-09 石家庄市长安育才建材有限公司 A kind of preparation method of the economization agent with water-reducing property
CN106587708A (en) * 2016-12-20 2017-04-26 浙江建研科之杰新材料有限公司 Polycarboxylate superplasticizer for pervious concrete and preparation method thereof
CN107540795A (en) * 2017-09-12 2018-01-05 上海三瑞高分子材料股份有限公司 A kind of shrinkage type polycarboxylate water-reducer and preparation method thereof
CN109956698A (en) * 2019-03-19 2019-07-02 雷洪伍 A kind of strong concrete economization agent
CN110746553A (en) * 2019-11-25 2020-02-04 中建西部建设新疆有限公司 Low-shrinkage viscosity-reduction type polycarboxylate superplasticizer and preparation method and application thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1300198C (en) * 2005-06-21 2007-02-14 重庆大学 Polyacrylic acid salts shrinkage-reducing-agent and method for making same
CN102040712A (en) * 2010-11-04 2011-05-04 江苏博特新材料有限公司 Preparation method of polymer shrinkage reducing agent with water-reducing function
CN105669919A (en) * 2016-01-14 2016-06-15 厦门路桥翔通建材科技有限公司 Polycarboxylate superplasticizer with high water retention and preparation method thereof
CN107417221A (en) * 2017-09-21 2017-12-01 张聪聪 Wear-resistant and crack-resistant cement-based self-leveling mortar and its production method

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103333297A (en) * 2013-06-24 2013-10-02 北京工业大学 Preparation method of reduced polycarboxylate-type high-performance water reducing agent
CN104592460A (en) * 2015-01-28 2015-05-06 南京瑞迪高新技术有限公司 Preparation method of reduction type polycarboxylate superplasticizer
CN104628972A (en) * 2015-01-30 2015-05-20 江苏奥莱特新材料有限公司 Preparation method of anti-crack shrinkage reducing polycarboxylate based superplasticizer
CN105601152A (en) * 2015-12-17 2016-05-25 江苏苏博特新材料股份有限公司 Efficient shrinkage-reducing anti-cracking agent and preparation method thereof
CN106084147A (en) * 2016-06-04 2016-11-09 石家庄市长安育才建材有限公司 A kind of preparation method of the economization agent with water-reducing property
CN106587708A (en) * 2016-12-20 2017-04-26 浙江建研科之杰新材料有限公司 Polycarboxylate superplasticizer for pervious concrete and preparation method thereof
CN107540795A (en) * 2017-09-12 2018-01-05 上海三瑞高分子材料股份有限公司 A kind of shrinkage type polycarboxylate water-reducer and preparation method thereof
CN109956698A (en) * 2019-03-19 2019-07-02 雷洪伍 A kind of strong concrete economization agent
CN110746553A (en) * 2019-11-25 2020-02-04 中建西部建设新疆有限公司 Low-shrinkage viscosity-reduction type polycarboxylate superplasticizer and preparation method and application thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
《减缩型聚羧酸减水剂的制备及减缩机理研究》;马建峰;《中国优秀硕士学位论文全文数据库,工程科技Ⅰ辑》;20200331;第B015-365页 *

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