Multifunctional cement hydration heat control material and manufacturing method therefor

Abstract

Disclosed are a multifunctional cement hydration heat control material and a manufacturing method therefor. The cement hydration heat control material in is a comb polymer having three side chain structures, the three side chain structures are respectively a carboxyl group, a sugar alcohol group, and a polyether structure, and the main chain of the polymer is a carbon chain structure formed by free-radical polymerization of a double bond in a double bond compound monomer. The multifunctional cement hydration heat control material can achieve integration of cement hydration heat control performance, water reduction performance, and shrinkage reduction performance in a same molecule, can achieve control focusing on a performance by means of structural adjustment, does not need multi-component compounding during use, and is more convenient. The control material is non-toxic and water-soluble, can be made to have an appropriate concentration, and is convenient to use.

Claims

1. A multifunctional material for controlling cement hydration heat, wherein the material for controlling cement hydration heat is a comb-shaped polymer with three kinds of side chain structures, and the three kinds of side chain structures are carboxyl groups, alditol groups, polyalkylene glycols, respectively; and a backbone of the polymer is a carbon chain structure formed through free radical polymerization of double bonds in double-bond compound monomers, wherein the multifunctional material for controlling cement hydration heat is prepared by free radical polymerization of monomers A, B, and C; the monomer A is a (methyl) acrylic acid (acrylate) monomer, the monomer B is a double-bond compound with one alditol group, and the monomer C is unsaturated polyether; and a weight-average molecular weight of the material for controlling cement hydration heat ranges from 10000 to 100000, wherein the monomer A has a structure represented by a general formula (1): ##STR00006## wherein R.sub.1 is methyl or H, and M is H or an alkali metal elements; the monomer B has a structure represented by a general formula as described below (2): ##STR00007## wherein R.sub.2 and R.sub.3 are each independently selected from a hydrogen atom or an alditol group, and R.sub.2 and R.sub.3 are identical to each other; and the monomer C has any one of three structures represented by a general formula (3): ##STR00008## wherein n and m are each 0 or a positive integer, and m and n are not 0 at the same time; and a weight-average molecular weight of the monomer C ranges from 500 to 10000.

2. The multifunctional material for controlling cement hydration heat as claimed in claim 1, wherein the multifunctional material for controlling cement hydration heat has a structure represented by a general formula (4): ##STR00009## wherein a, b and c are positive integers.

3. The multifunctional material for controlling cement hydration heat as claimed in claim 2, wherein the M is H, Na, or K.

4. The multifunctional material for controlling cement hydration heat as claimed in claim 1, wherein the monomer B is a compound or a mixture formed by a ring-opening addition reaction of allyl glycidyl ether and an alditol compound in a molar ratio of 1:1, and the alditol compound is selected from the group consisting of sorbitol, xylitol, mannitol, erythritol, lactitol, maltitol, and combinations thereof in any proportion.

5. The multifunctional material for controlling cement hydration heat as claimed in claim 1, wherein the monomer C is formed by ring-opening polymerization of olefinic alcohol and epoxy alkane in any proportion, wherein the epoxy alkane is any one of epoxy ethane, epoxy propane, or a mixture thereof in any proportion; when the epoxy alkane contains epoxy ethane and epoxy propane, the monomer C is prepared by ring-opening polymerization of olefinic alcohol with epoxy ethane and then with epoxy propane in any proportion, and neither m nor n is 0; when the monomer C is formed by ring opening polymerization of olefinic alcohol and epoxy ethane, m is 0; and when the monomer C is prepared by ring opening polymerization of olefinic alcohol and epoxy propane, n is 0; and the olefinic alcohol has any one of the structures represented by a general formula (5): ##STR00010##

6. A method for preparing the multifunctional material for controlling cement hydration heat as claimed in claim 1, the method comprising the following steps: performing free radical polymerization of the monomer A, B, and C in water in presence of an initiator and a chain transfer agent, wherein a total weight of the monomer A, the monomer B and the monomer C accounts for 20% to 50% of a weight of a whole reaction system; a mass of the initiator ranges from 0.5% to 2.0% of the total weight of the monomer A, the monomer B, and the monomer C; and the chain transfer agent is mercaptoethanol or mercaptoacetic acid, and a mass of the chain transfer agent ranges 0% to 1.0% of the total weight of the monomer A, the monomer B and the monomer C.

7. The method for preparing the multifunctional material for controlling cement hydration heat as claimed in claim 6, wherein the initiator is any one of ammonium persulfate, sodium persulfate, potassium persulfate, or a mixture thereof in any proportion.

8. The method for preparing the multifunctional material for controlling cement hydration heat as claimed in claim 6, wherein the initiator is a redox system, in which an oxidant is hydrogen peroxide, and a reductant agent is alkali metal sulfite or ascorbic acid.

Description

BRIEF DESCRIPTION OF THE FIGURES

(1) FIG. 1 illustrates results of evaluation on cement hydration heat release rate of cement hydration heat control materials prepared in Example 1 and Comparative Example 1;

(2) FIG. 2 illustrates results of evaluation on cement hydration heat release rate of cement hydration heat control materials prepared in Example 2 and Comparative Example 2 as well as Comparative Example 4; and

(3) FIG. 3 illustrates results of evaluation on cement hydration heat release rate of cement hydration heat control materials prepared in Example 3 and Comparative Example 3.

DETAILED DESCRIPTION OF EMBODIMENTS

(4) In order to better understand the present disclosure, it will be further explained with examples below. However, the present disclosure shall not be limited to the scope defined by these examples. All monomers in the embodiments of the present disclosure can be purchased commercially, or can be prepared according to the conventional operations in the field as described in the present disclosure. Molecular weight of the product of the present disclosure is a weight-average molecular weight measured by a gel permeation chromatograph instrument. In product performance test of the present disclosure, the cement is a reference cement meeting the requirements under GB8076, a fluidity test of cement paste is carried out according to GB8077 with 87 g water added; a 7-day shrinkage rate test of mortar is carried out according to JC/T 2361-2016; the hydration heat performance is obtained by a TAM-AIR isothermal calorimeter (TA Instruments, USA) measuring the hydration heat release rate of the cement over time, the test temperature is 20? C., the test object is cement paste, and the water-binder ratio is 0.4.

Example 1

(5) 1) Preparation of a monomer B.sub.1: 0.1 mol (11.4 g) of allyl glycidyl ether and 0.1 mol of mannitol were blended. A ring-opening addition reaction was carried out under the action of an alkaline catalyst at a high temperature to obtain 0.1 mol of a mannitol-based monomer B.sub.1. 2) Preparation of the multifunctional cement hydration heat control material: 0.1 mol of the above monomer B.sub.1, 0.1 mol of methacrylic acid (monomer A.sub.1, where R.sub.1 was methyl), 0.2 mol of polyethylene glycol monoallyl alcohol ether (monomer C.sub.1, with a weight-average molecular weight about 500, where n=10, m=0), and mercaptoethanol accounting for 0.5% of the total mass of the three monomers were prepared as an aqueous solution, which was vacuumized and replaced by nitrogen for several times; the temperature was raised to 80? C., an aqueous solution of ammonium persulfate was added dropwise while stirring. Afterwards, the temperature was kept for 2 h. The solution was then cooled to the room temperature, an alkali was added to neutralize the solution to a pH value of 7.4, thus obtaining the multifunctional cement hydration heat control material with a weight-average molecular weight of 15,000 (Example 1).

Example 2

(6) 1) Preparation of monomer B2: 0.1 mol (11.4 g) of allyl glycidyl ether, 0.05 mol of sorbitol and 0.05 mol of lactitol were blended, and a ring-opening addition reaction was carried out under the action of an alkaline catalyst at a high temperature to obtain 0.1 mol of an alditol-based monomer B.sub.2. 2) Preparation of a multifunctional cement hydration heat control material: 0.1 mol of the above monomer B.sub.2, 0.2 mol of sodium acrylate (monomer A.sub.2, where R.sub.1 was H), 0.25 mol of polypropylene glycol monoisoamylene alcohol ether (monomer C.sub.2, with a weight-average molecular weight about 5000, where n=86, m=20), mercaptoethanol accounting for 1.0% of the total mass of the three monomers, and 0.5% hydrogen peroxide were prepared as an aqueous solution, which was vacuumized and replaced by nitrogen for several times; the temperature was raised to 40? C., an aqueous solution of ascorbic acid with the same molar amount as hydrogen peroxide was added dropwise while stirring, and afterwards, the temperature was kept for 2 h. The solution was then cooled to the room temperature, thus obtaining the multifunctional cement hydration heat control material with a weight-average molecular weight of 100,000 (Example 2).

Example 3

(7) 1) Preparation of a monomer B.sub.3: 0.1 mol (11.4 g) of allyl glycidyl ether, 0.02 mol of mannitol, 0.02 mol of xylitol, and 0.06 mol of maltitol were blended, and a ring-opening addition reaction was carried out under the action of an alkaline catalyst at a high temperature to obtain 0.1 mol of an alditol-based monomer B.sub.3. 2) Preparation of a multifunctional cement hydration heat control material: 0.1 mol of the above monomer B.sub.3, 0.05 mol of acrylic acid, 0.01 mol of potassium methacrylate (monomer A.sub.3, where R.sub.1 was methyl), 0.05 mol of polypropylene glycol monoisobutylene alcohol ether (monomer C.sub.3, with a weight-average molecular weight about 1000, where n=0, m=16), and thioglycolic acid accounting for 0.2% of the total mass of the three monomers were prepared as an aqueous solution, which was vacuumized and replaced by nitrogen for several times; the temperature was raised to 80? C., an aqueous solution of sodium persulfate was added dropwise while stirring, and afterwards, the temperature was kept for 2 h; the solution was then cooled to the room temperature, and an alkali was added to neutralize the solution to a pH value of 7.4, thus obtaining the multifunctional cement hydration heat control material with a weight-average molecular weight of 80,000 (Example 3).

Comparative Example 1

(8) In the preparation of the multifunctional cement hydration heat control material in Example 1, the monomer Blin the above reaction was replaced by an equal molar amount of allyl glycerol ether, while other conditions kept unchanged, and a copolymer was prepared.

Comparative Example 2

(9) In the preparation of the multifunctional cement hydration heat control material in Example 2, the monomer B.sub.2 in the above reaction was replaced by an equal molar amount of allyl glycerol ether, while other conditions kept unchanged, and a copolymer was prepared.

Comparative Example 3

(10) In the preparation of the multifunctional cement hydration heat control material in Example 3, the monomer B.sub.3 in the above reaction was replaced by an equal molar amount of allyl glycerol ether, while other conditions kept unchanged, and a copolymer was prepared.

Comparative Example 4

(11) With reference to Japanese Patent JP2003034564A, a starch-based compound with a solubility of 6% in water at 50? C. and 40% in water at 80? C. was prepared.

(12) With the same dosage (an effective content of copolymer accounts for 0.2% of the cement weight) of the multifunctional cement hydration heat control materials according to the present disclosure and the control materials prepared in respective comparative examples, the fluidity of the cement paste and the shrinkage reduction performance of the mortar are shown in Table 1 below. The fluidity of the reference cement paste was only 70 mm, indicating no fluidity. In contrast, the fluidity of the paste added with the samples of the examples of the present disclosure and comparative examples was obviously increased to over 200 mm, indicating significant water reducing property of this structure. At the same time, due to the different structures of polyether segments, the 7-day shrinkage reduction rate of mortar shows obvious shrinkage reduction characteristics by adding different samples varies, and the copolymer containing polyether with a side chain and a polypropylene glycol structure. However, the starch-based compound prepared according to Japanese Patent JP2003034564A had negligible effect on the fluidity of the cement paste and the 7-day shrinkage reduction rate of the mortar.

(13) TABLE-US-00001 TABLE 1 Test Performance No Comparative Comparative Comparative Comparative Samples Copolymer Example 1 Example 1 Example 2 Example 2 Example 3 Example 3 Example 4 Fluidity 70 240 235 220 215 205 205 75 of the cement paste/mm 7-day 0 5 5 35 32 25 20 0 shrinkage reduction rate of mortar/%

(14) With the same dosage (the effective content of the copolymer accounts for 0.25% of the cement weight) of the multifunctional hydration heat control materials prepared in the examples of the present disclosure and comparative examples, the hydration heat release rate performance of the cement at 20? C. is shown in FIG. 1, FIG. 2 and FIG. 3. FIG. 1 illustrates the heat release rates of the paste mixed with the samples in Example 1 and Comparative Example 1 to characterize the influence of the products on cement hydration. The heat release rate of the reference paste (without any sample) increases rapidly after adding water, and reaches the peak value (about 2.4 mW/g) quickly; the heat release rate curve of the paste mixed with the sample according to the Comparative Example 1 also rises rapidly after a relatively short induction period, and quickly reaches the peak value (about 2.2 mW/g), this value is slightly lower than the reference sample; regarding the paste doped with the sample of Example 1 of the present disclosure, the time taken to reach the peak heat release is relatively long, and the peak value of the heat release rate is significantly reduced to around 1.4 mW/g. Compared with the peak values of the reference group and those of the comparative examples, this number is decreased by more than 35% showing an obvious effect on controlling the hydration heat of cement hydration. At the same time, during the temperature drop stage, the three curves are different, and the temperature drop rates decrease in a sequent of reference group, the Comparative Example 1 group, and the Example 1 group, indicating that the technology described in the present disclosure can also adjust the performance of the cement in the later stage of hydration heat release. With reference to FIG. 2, the hydration rate curves of different groups of the paste reveals that, compared with the reference group, the peak hydration rate of the Comparative Example 2 group decreases by 14%, the peak hydration rate of the comparative example 4 group related to the Japanese Patent decreases by 24%, and the peak hydration rate of the Example 2 group of the present disclosure decreased by 58%; from the declining stage of the hydration rate curve, the hydration rate curve of the cement of Comparative Example 2 is basically the same as the reference group, and the hydration rate of the cement decreases rapidly, while the curve of comparative example 4 in Japanese patent technology is slightly gentle, the hydration rate decreases slowly, and the hydration rate in the Example 2 of the present disclosure is the slowest. As shown in FIG. 3, compared with the reference group, the peak hydration rate of Comparative Example 3 group decreases by 19%, and the peak hydration rate of Example 3 group decreases by 74%; in the hydration rate decreasing stage, the decrease in the Example 3 of the present disclosure is obviously less than that in the reference group and the comparative example groups, meanwhile the comparative example groups are basically consistent with the reference group.

(15) In conclusion, on basis of the results of the cement paste fluidity, 7-day shrinkage reduction rate of the mortar, and cement hydration heat release rate, the present disclosure can realize multiple functions including water reduction, shrinkage reduction and hydration heat control.