CN111454013A - Stabilizer for liquid alkali-free accelerator and preparation method thereof - Google Patents
Stabilizer for liquid alkali-free accelerator and preparation method thereof Download PDFInfo
- Publication number
- CN111454013A CN111454013A CN202010269477.5A CN202010269477A CN111454013A CN 111454013 A CN111454013 A CN 111454013A CN 202010269477 A CN202010269477 A CN 202010269477A CN 111454013 A CN111454013 A CN 111454013A
- Authority
- CN
- China
- Prior art keywords
- stabilizer
- liquid alkali
- free accelerator
- free
- alkali
- 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.)
- Granted
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 96
- 239000003381 stabilizer Substances 0.000 title claims abstract description 66
- 238000002360 preparation method Methods 0.000 title abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 238000000034 method Methods 0.000 claims abstract description 17
- 230000008719 thickening Effects 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 9
- 239000013008 thixotropic agent Substances 0.000 claims abstract description 9
- 239000007787 solid Substances 0.000 claims abstract description 3
- 238000006243 chemical reaction Methods 0.000 claims description 47
- 238000003756 stirring Methods 0.000 claims description 38
- 239000006185 dispersion Substances 0.000 claims description 24
- -1 polyethylene Polymers 0.000 claims description 19
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical group OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 13
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 claims description 11
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 11
- 239000013078 crystal Substances 0.000 claims description 11
- 229940102253 isopropanolamine Drugs 0.000 claims description 11
- 229920000805 Polyaspartic acid Polymers 0.000 claims description 8
- 239000004698 Polyethylene Substances 0.000 claims description 8
- 108010064470 polyaspartate Proteins 0.000 claims description 8
- 229920000573 polyethylene Polymers 0.000 claims description 8
- 238000002791 soaking Methods 0.000 claims description 8
- BAERPNBPLZWCES-UHFFFAOYSA-N (2-hydroxy-1-phosphonoethyl)phosphonic acid Chemical compound OCC(P(O)(O)=O)P(O)(O)=O BAERPNBPLZWCES-UHFFFAOYSA-N 0.000 claims description 7
- 229920001529 polyepoxysuccinic acid Polymers 0.000 claims description 7
- 239000008139 complexing agent Substances 0.000 claims description 6
- 239000002270 dispersing agent Substances 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 229940120146 EDTMP Drugs 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000004359 castor oil Substances 0.000 claims description 4
- 235000019438 castor oil Nutrition 0.000 claims description 4
- NFDRPXJGHKJRLJ-UHFFFAOYSA-N edtmp Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCN(CP(O)(O)=O)CP(O)(O)=O NFDRPXJGHKJRLJ-UHFFFAOYSA-N 0.000 claims description 4
- 229910021485 fumed silica Inorganic materials 0.000 claims description 4
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 4
- 239000004952 Polyamide Substances 0.000 claims description 3
- 239000000440 bentonite Substances 0.000 claims description 3
- 229910000278 bentonite Inorganic materials 0.000 claims description 3
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000003607 modifier Substances 0.000 claims 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 abstract description 21
- 238000004519 manufacturing process Methods 0.000 abstract description 6
- 230000008569 process Effects 0.000 abstract description 6
- 238000010276 construction Methods 0.000 description 13
- AMVQGJHFDJVOOB-UHFFFAOYSA-H aluminium sulfate octadecahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O AMVQGJHFDJVOOB-UHFFFAOYSA-H 0.000 description 12
- 229940043237 diethanolamine Drugs 0.000 description 12
- 239000004567 concrete Substances 0.000 description 10
- 229910052731 fluorine Inorganic materials 0.000 description 9
- 239000011737 fluorine Substances 0.000 description 9
- 239000003513 alkali Substances 0.000 description 8
- 239000011378 shotcrete Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 230000007797 corrosion Effects 0.000 description 7
- 238000005260 corrosion Methods 0.000 description 7
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 6
- 238000004090 dissolution Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000006378 damage Effects 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 230000001737 promoting effect Effects 0.000 description 4
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 210000001519 tissue Anatomy 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 2
- 229910001634 calcium fluoride Inorganic materials 0.000 description 2
- 230000000536 complexating effect Effects 0.000 description 2
- 238000010668 complexation reaction Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000005189 flocculation Methods 0.000 description 2
- 230000016615 flocculation Effects 0.000 description 2
- 150000004673 fluoride salts Chemical class 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 235000013024 sodium fluoride Nutrition 0.000 description 2
- 239000011775 sodium fluoride Substances 0.000 description 2
- 230000009974 thixotropic effect Effects 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 102000001554 Hemoglobins Human genes 0.000 description 1
- 108010054147 Hemoglobins Proteins 0.000 description 1
- 208000013038 Hypocalcemia Diseases 0.000 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- 208000006735 Periostitis Diseases 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- 206010037423 Pulmonary oedema Diseases 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 102000019259 Succinate Dehydrogenase Human genes 0.000 description 1
- 108010012901 Succinate Dehydrogenase Proteins 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000003044 adaptive effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000004931 aggregating effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 210000000748 cardiovascular system Anatomy 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 231100000481 chemical toxicant Toxicity 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000003278 haem Chemical class 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 230000000705 hypocalcaemia Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009440 infrastructure construction Methods 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- 238000006213 oxygenation reaction Methods 0.000 description 1
- 210000003460 periosteum Anatomy 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 208000005333 pulmonary edema Diseases 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 230000004202 respiratory function Effects 0.000 description 1
- 108010048734 sclerotin Proteins 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- 210000000434 stratum corneum Anatomy 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B40/00—Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
- C04B40/0028—Aspects relating to the mixing step of the mortar preparation
- C04B40/0039—Premixtures of ingredients
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
The invention belongs to the technical field of alkali-free accelerator auxiliaries, and particularly relates to a stabilizer for a liquid alkali-free accelerator and a preparation method thereof, wherein the stabilizer comprises the following components in percentage by solid content: 3% -9% of thickening thixotropic agent; the liquid alkali-free accelerator stabilizer prepared by the invention is a liquid mixture with consistency, and when the stabilizer is used for producing the liquid alkali-free accelerator, the stabilizer, aluminum sulfate and water are only stirred and fully dissolved to obtain the liquid alkali-free accelerator which meets the national standard and is constructed by utilizing the method, the production equipment and the process are simple, and the normal-temperature production is realized.
Description
Technical Field
The invention belongs to the technical field of alkali-free accelerator auxiliaries, and particularly relates to a stabilizer for a liquid alkali-free accelerator and a preparation method thereof.
Background
The accelerator is a chemical additive for quickly setting and hardening concrete, is an essential key material in concrete spraying construction, is widely applied to engineering construction such as tunnel support, mine reinforcement, road first-aid repair, waterproof plugging and the like, and plays an important role in the national infrastructure construction industry. The quick-setting admixture is divided into two types of powder quick-setting admixture and liquid quick-setting admixture, the powder quick-setting admixture is mainly used for dry-process sprayed concrete, the dry spraying has the defects of large dust, uneven doping, high resilience and the like, and the powder quick-setting admixture is abandoned in tunnel engineering construction gradually. The liquid accelerator is mainly used for wet sprayed concrete, has the advantages of better construction environment, low rebound rate of sprayed concrete, high construction quality and the like compared with a wet spraying process of a dry spraying process, is more and more important due to the improvement of requirements of engineering durability indexes, environmental protection and the like, and has the market share increased from 3.1% in 2013 to 63.3% in 2015, which gradually replaces a powder accelerator.
The liquid accelerator can be divided into an alkali liquid accelerator and an alkali-free (low-alkali) liquid accelerator according to the alkali metal content, the two liquid accelerators have obvious differences in the aspects of raw material selection, preparation method, performance characteristics and accelerating mechanism, the alkali liquid accelerator plays an important role in construction application for many years, but has the serious problems of high concrete alkali-aggregate reaction probability, insufficient 28-day compressive strength ratio, damage to the health of constructors and the like, the alkali-free liquid accelerator solves the problem of high alkali content of the traditional accelerator, reduces the possibility of alkali-aggregate reaction of sprayed concrete, the 28d strength ratio of the concrete doped with the alkali-free liquid accelerator can reach more than 90 percent, and in addition, the alkali-free liquid accelerator has no corrosion, is friendly to construction environment and has little harm to the body of construction workers. Therefore, the alkali-free liquid accelerator tends to replace the alkali accelerator.
In order to increase the concentration of aluminum sulfate in a liquid phase system as much as possible, NaF and NaHF are mostly used in the existing alkali-free accelerator products2Fluorine-containing compounds such as HF or fluosilicate promote the dissolution of aluminum sulfate and the stabilization of a liquid phase system, but larger potential safety and quality hazards still exist in the actual production and application. First, HF is a highly harmful poison to the clothingThe fluorine ions can be combined with calcium and magnesium ions in blood or tissues to form insoluble or slightly soluble calcium fluoride and magnesium fluoride, if the fluorine ions are in large quantity, the blood vessels are directly blocked, the functions of the central nervous system and the cardiovascular system are directly or indirectly influenced, so that hypocalcemia and hypomagnesian syndrome are caused, the fluorine ions can be combined with hemoglobin to form heme, succinic dehydrogenase is inhibited, oxygenation is reduced, and the respiratory function of cells is influenced. In addition, hydrofluoric acid can cause obvious burns at the contact part, dehydrate and dissolve tissue protein, quickly penetrate stratum corneum, infiltrate into deep tissues, dissolve cell membranes, cause tissue liquefaction, and deeply reach periosteum and sclerotin to enable bones to become calcium fluoride and form ulcer with slow healing. Inhalation of high concentrations of vapor or transdermal absorption can cause chemical pneumonic pulmonary edema. NaHF2Is also a strongly acidic, toxic chemical, and releases HF upon absorption of moisture in humid air. Fluorosilicates such as magnesium fluorosilicate, sodium fluorosilicate, etc. also belong to chemical substances which can cause poisoning when inhaled or taken by human body, and react with acids to release HF. Therefore, the fluorine-containing compound used in the alkali-free accelerator has great potential safety hazard and can cause serious physiological injury which is difficult to reverse for production and testing personnel who are contacted for a long time. And secondly, hydrofluoric acid has extremely strong corrosivity and can strongly corrode metal and glass products. May corrode the steel bars in the concrete and seriously harm the engineering quality. In addition, the alkali-free accelerator product using the fluorine-containing compound has the problem of insufficient strength of concrete in one day in practical application, and has the major potential safety hazard that the whole of the primary tunnel support sprayed concrete in the previous procedure falls to hurt people when drilling and blasting are carried out in tunnel construction. Therefore, the alkali-free accelerator produced by using fluoride has the potential safety and quality hazards although the liquid phase system is relatively stable, the aluminum sulfate content is high, and the accelerating effect is good. For example, patent No. CN201710101536.6 discloses that the alkali-free accelerator contains sodium fluoride. Further, for example, patent No. CN201610483075.9 discloses an environment-friendly low-resilience low-alkali liquid accelerator and a preparation method thereof, although it is disclosed that fluoride salt is dissolved in nano-silica dispersion and utilizedThe modified fluoride salt is obtained by high-shear stirring, but the defects brought by the fluoride can not be overcome.
However, if the alkali-free accelerator product without the fluorine-containing compound is used, the problems of insufficient concentration of effective accelerating substances, poor accelerating effect or poor stability of a liquid system exist, which mainly show that a large amount of clear liquid appears on the surface of the product or large-particle crystals are generated in the product, a filter screen of a supply pipeline of a mechanical grouting accelerator is easily blocked in actual use, the accelerator is difficult to suck, and the construction effect of spraying concrete is poor. For example, patent No. CN201810444470.5 discloses an alkali-free liquid accelerator and a preparation method thereof, wherein the alkali-free liquid accelerator is composed of the following raw materials by mass percent: 45% -55% of aluminum sulfate, 3% -5% of diethanolamine, 3% -5% of triethanolamine, 3% -5% of glycerol, 0.3% -0.5% of stabilizing agent, 0.3% -0.5% of sodium sulfate, 0.2% -0.4% of magnesium aluminum silicate, 0.01% -0.04% of high-molecular thickening agent and 28.6% -45.2% of water, wherein a scheme without fluorine is disclosed, but the scheme has more components and narrow range sources of raw materials; for another example, patent No. CN201910979194.7 discloses a low temperature resistant liquid alkali-free accelerator and a preparation method thereof, wherein the accelerator comprises the following components by mass percent: 40-50% of aluminum sulfate, 5-10% of alcohol amine, 0.01-0.05% of stabilizer, 4-6% of reinforcing agent, 1-2% of modified nano material, 1-2% of pH regulator and 29.95-48.99% of water, wherein a scheme without fluorine is disclosed, but the scheme has long preparation process time consumption and more control requirements.
Disclosure of Invention
The invention provides a stabilizer for a liquid alkali-free accelerator and a preparation method thereof, aiming at solving the problem of poor system stability of a fluoride-free alkali-free accelerator product. The liquid alkali-free accelerator is added with 10-20 percent of the stabilizer for the liquid alkali-free accelerator according to the requirements, 50-65 percent of aluminum sulfate and the balance of water are fully stirred and dissolved, and insoluble impurities are filtered to obtain a product meeting the requirements of the alkali-free accelerator in the national standard GB/T35159-2017 accelerator for sprayed concrete, and large-particle crystals are not easy to appear to influence the actual construction.
The method is realized by the following technical scheme:
a stabilizer for a liquid alkali-free accelerator comprises the following components in percentage by solid content: 3% -9% of thickening thixotropic agent; 20-50% of organic complexing agent, 5-15% of organic early strength agent, less than or equal to 2% of macromolecular dispersing agent, less than or equal to 10% of crystal form regulator and the balance of water.
Further, the thickening thixotropic agent is any one or more of fumed silica, organic bentonite, hydrogenated castor oil, polyamide wax and polyethylene wax; the liquid alkali-free accelerator stabilizer has good thixotropic property in liquid, the liquid consistency is increased after standing, suspended substances in the liquid are not easy to sink, and the liquid fluidity can be recovered by slightly stirring before the alkali-free accelerator is used, so that the liquid alkali-free accelerator stabilizer has the functions of physical thickening and anti-settling and thixotropic recovery of the flow property of a system.
Furthermore, the organic complexing agent is diethanol amine, aluminum sulfate is easy to dissolve in water, but the solubility is not high at normal temperature, 36.4g of aluminum sulfate can be dissolved in L m of water at 20 ℃, the concentration can not meet the requirement of quick setting of sprayed concrete, so that the aluminum sulfate dissolution is promoted by the organic complexing agent diethanol amine, the content of aluminum sulfate in the alkali-free accelerator is increased, and the liquid alkali-free accelerator stabilizer has the function of promoting the dissolution by chemical complexation.
Further, the organic early strength agent is one or a mixture of triethanolamine and isopropanolamine. The triethanolamine or the isopropanolamine is added into the concrete, so that the development of early strength is facilitated, the maintenance of later strength is not influenced, and the triethanolamine or the isopropanolamine can promote the dissolution of aluminum sulfate through a complexing reaction. Therefore, the liquid alkali-free accelerator stabilizer has the functions of improving the one-day strength of sprayed concrete and promoting dissolution by chemical complexation.
Further, the polymeric dispersant is: one or more of polyepoxysuccinic acid with molecular weight ranging from 400 to 1500, polyepoxysuccinic acid salt with molecular weight ranging from 400 to 1500 and polyaspartic acid with molecular weight ranging from 1000 to 5000. The polymer dispersant can be adsorbed on the surface of aluminum sulfate particles, and prevents the aluminum sulfate particles from further aggregating through surface charge repulsion to generate sedimentation; therefore, the stabilizer for the liquid alkali-free accelerator has the function of dispersing aluminum sulfate particles.
Further, the crystal form regulator is any one or more of aminotrimethylene methylene phosphoric acid, hydroxy ethylidene diphosphonic acid and ethylene diamine tetramethylene phosphonic acid. Such materials can affect the process of aluminum sulfate crystal formation in supersaturated solutions, adjusting aluminum sulfate crystal morphology. Therefore, the liquid alkali-free accelerator stabilizer has the function of adjusting the crystal form.
Further, the preparation method of the stabilizer for the liquid alkali-free accelerator comprises the following steps:
1) adding the thickening thixotropic agent and water into a reaction kettle, stirring at low speed for 10-15min, stopping stirring, and soaking for 10-15 min; 2) adding the rest components into a reaction kettle, and stirring at low speed for 10-15min to mix thoroughly; 3) dispersing at high speed for 10-15min to obtain liquid alkali-free accelerator stabilizer; wherein the linear speed of the edge of the paddle reaches 18m/s during high-speed dispersion.
The invention also provides another preparation method of the stabilizer for the liquid alkali-free accelerator, which comprises the following steps: adding the thickening thixotropic agent and water into a reaction kettle, adding other components into the reaction kettle, and stirring until the components are uniform to obtain the liquid alkali-free accelerator stabilizer.
The invention has the advantages that:
1. the liquid alkali-free accelerator stabilizer prepared by the invention is a liquid mixture with consistency, when the stabilizer, aluminum sulfate and water are stirred when the stabilizer is used for producing the liquid alkali-free accelerator, the liquid alkali-free accelerator which meets the national standard and is constructed by utilizing can be obtained after the stabilizer, the aluminum sulfate and the water are fully dissolved, the production equipment and the process are simple, and the normal-temperature production is realized.
2. The liquid alkali-free accelerator stabilizer prepared by the invention has the functions of preventing physical thickening, dispersing charge repulsion force and adjusting crystal form, can prevent supersaturated aluminum sulfate solution from separating out crystals, and can prevent a suspension system of the alkali-free accelerator from being layered and settled in a large quantity.
3. The stabilizer for the liquid alkali-free accelerator has chemical complexing dissolution promoting performance, can improve the solubility of aluminum sulfate in a liquid phase system, and improves the coagulation promoting effect of the liquid alkali-free accelerator.
4. The liquid alkali-free accelerator stabilizer prepared by the invention has the function of improving the strength of concrete, and does not influence the later strength development of the concrete.
5. The liquid alkali-free accelerator stabilizer prepared by the invention has good consistency, can prevent sedimentation, can restore good fluidity before use, and is convenient for construction.
Detailed Description
The following is a detailed description of the embodiments of the present invention, but the present invention is not limited to these embodiments, and any modifications or substitutions in the basic spirit of the embodiments are included in the scope of the present invention as claimed in the claims.
Example 1
The embodiment provides a preparation method of a stabilizer for a liquid alkali-free accelerator, which comprises the following steps:
1. preparing a high-speed dispersion machine and an acid-base corrosion resistant reaction kettle, wherein the stirring paddle is disc-shaped, and the highest linear speed of the edge of the paddle meets 18 m/s;
2. adding 40g of fumed silica and 350g of water into a reaction kettle, stirring at a low speed for 10 minutes, stopping stirring, and soaking for 10 minutes;
3. adding 550g of diethanolamine, 50g of isopropanolamine and 10g of polyepoxysuccinic acid with the molecular weight of 400 into a reaction kettle, starting the reaction kettle, stirring at a low speed for 10 minutes, and fully and uniformly mixing;
4. starting high-speed dispersion, wherein the linear velocity of the edge of the paddle reaches 18m/s during the high-speed dispersion, and obtaining the stabilizer for the liquid alkali-free setting accelerator after the high-speed dispersion is carried out for 10 minutes;
the embodiment also provides a method for preparing the liquid alkali-free accelerator by using the stabilizer, which comprises the following steps:
adding 250g of water into a reaction kettle, adding 150g of a stabilizer for a liquid alkali-free setting accelerator, and stirring for 10 minutes; and slowly adding 600g of aluminum sulfate octadecahydrate into the reaction kettle, and continuously stirring until the aluminum sulfate octadecahydrate is completely dissolved to obtain the liquid alkali-free accelerator.
Example 2
The embodiment provides a preparation method of a stabilizer for a liquid alkali-free accelerator, which comprises the following steps:
1. preparing a high-speed dispersion machine and an acid-base corrosion resistant reaction kettle, wherein the stirring paddle is disc-shaped, and the highest linear speed of the edge of the paddle meets 18 m/s;
2. adding 50g of polyamide wax and 350g of water into a reaction kettle, stirring at a low speed for 15 minutes, stopping stirring, and soaking for 15 minutes;
3. adding 450g of diethanolamine, 40g of isopropanolamine, 40g of triethanolamine, 20g of polyepoxysuccinic acid with the molecular weight of 1500 and 50g of aminotrimethylene methylene phosphonic acid into a reaction kettle, starting the reaction kettle, stirring at a low speed for 15 minutes, and fully and uniformly mixing;
4. starting high-speed dispersion, wherein the linear velocity of the edge of the paddle reaches 18m/s during the high-speed dispersion, and obtaining the stabilizer for the liquid alkali-free setting accelerator after the high-speed dispersion is carried out for 15 minutes;
the embodiment also provides a method for preparing the liquid alkali-free accelerator by using the stabilizer, which comprises the following steps:
adding 250g of water into a reaction kettle, adding 150g of a stabilizer for a liquid alkali-free setting accelerator, and stirring for 10 minutes; and slowly adding 600g of aluminum sulfate octadecahydrate into the reaction kettle, and continuously stirring until the aluminum sulfate octadecahydrate is completely dissolved to obtain the liquid alkali-free accelerator.
Example 3
The embodiment provides a preparation method of a stabilizer for a liquid alkali-free accelerator, which comprises the following steps:
1. preparing a high-speed dispersion machine and an acid-base corrosion resistant reaction kettle, wherein the stirring paddle is disc-shaped, and the highest linear speed of the edge of the paddle meets 18 m/s;
2. adding 60g of polyethylene wax and 420g of water into a reaction kettle, stirring at a low speed for 12 minutes, stopping stirring, and soaking for 12 minutes;
3. adding 350g of diethanolamine, 50g of isopropanolamine, 60g of triethanolamine, 10g of polyaspartic acid with the molecular weight of 5000 and 50g of hydroxyethylidene diphosphonic acid into a reaction kettle, starting a low speed and stirring for 10-15 minutes, and fully and uniformly mixing;
4. starting high-speed dispersion, wherein the linear velocity of the edge of the paddle reaches 18m/s during the high-speed dispersion, and obtaining the stabilizer for the liquid alkali-free setting accelerator after the high-speed dispersion is carried out for 13 minutes;
the embodiment also provides a method for preparing the liquid alkali-free accelerator by using the stabilizer, which comprises the following steps:
adding 250g of water into a reaction kettle, adding 150g of a stabilizer for a liquid alkali-free setting accelerator, and stirring for 10 minutes; then 600g of aluminum sulfate octadecahydrate is slowly added into the reaction kettle, and the mixture is continuously stirred until the aluminum sulfate octadecahydrate is completely dissolved, so that the liquid alkali-free accelerator is obtained.
Example 4
The embodiment provides a preparation method of a stabilizer for a liquid alkali-free accelerator, which comprises the following steps:
1. preparing an acid and alkali corrosion resistant reaction kettle with a stirring paddle;
2. adding 70g of organic bentonite and 460g of water into a reaction kettle for soaking for 10-15 minutes;
3. adding 250g of diethanolamine, 150g of triethanolamine, 20g of polyaspartic acid with the molecular weight of 1000 and 50g of ethylenediamine tetramethylene phosphonic acid into a reaction kettle, starting the reaction kettle, and stirring uniformly to obtain the stabilizer for the liquid alkali-free accelerator;
the embodiment also provides a method for preparing the liquid alkali-free accelerator by using the stabilizer, which comprises the following steps:
adding 250g of water into a reaction kettle, adding 150g of a stabilizer for a liquid alkali-free setting accelerator, and stirring for 10 minutes; then 600g of aluminum sulfate octadecahydrate is slowly added into the reaction kettle, and the mixture is continuously stirred until the aluminum sulfate octadecahydrate is completely dissolved, so that the liquid alkali-free accelerator is obtained.
Example 5
The embodiment provides a preparation method of a stabilizer for a liquid alkali-free accelerator, which comprises the following steps:
1. preparing an acid and alkali corrosion resistant reaction kettle with a stirring paddle;
2. adding 25g of hydrogenated castor oil, 45g of polyethylene wax and 460g of water into a reaction kettle, and soaking for 10-15 minutes;
3. adding 250g of diethanolamine, 50g of triethanolamine, 100g of isopropanolamine, 5g of polyaspartic acid with the molecular weight of 2000, 15g of polyepoxysuccinate with the molecular weight of 1000, 20g of aminotrimethylene methylene phosphoric acid, 15g of hydroxyethylidene diphosphonic acid and 15g of ethylene diamine tetramethylene phosphonic acid into a reaction kettle, starting stirring until the mixture is uniform, and obtaining the stabilizer for the liquid alkali-free accelerator;
the embodiment also provides a method for preparing the liquid alkali-free accelerator by using the stabilizer, which comprises the following steps:
adding 250g of water into a reaction kettle, adding 150g of a stabilizer for a liquid alkali-free setting accelerator, and stirring for 10 minutes; then 600g of aluminum sulfate octadecahydrate is slowly added into the reaction kettle, and the mixture is continuously stirred until the aluminum sulfate octadecahydrate is completely dissolved, so that the liquid alkali-free accelerator is obtained.
Example 6
The embodiment provides a preparation method of a stabilizer for a liquid alkali-free accelerator, which comprises the following steps:
1. preparing a high-speed dispersion machine and an acid-base corrosion resistant reaction kettle, wherein the stirring paddle is disc-shaped, and the highest linear speed of the edge of the paddle meets 18 m/s;
2. adding 50g of hydrogenated castor oil, 20g of fumed silica and 460g of water into a reaction kettle, stirring at a low speed for 10-15 minutes, stopping stirring, and soaking for 10-15 minutes;
3. adding 250g of diethanolamine, 150g of isopropanolamine, 20g of polyepoxysuccinic acid sodium salt with the molecular weight of 1500, 20g of aminotrimethylene methylene phosphoric acid and 30g of hydroxyethylidene diphosphonic acid into the reaction kettle, stirring for 10-15 minutes, starting high-speed dispersion, wherein the linear velocity of the edge of a paddle reaches 18m/s during high-speed dispersion, and obtaining the stabilizer for the liquid alkali-free accelerator after high-speed dispersion for 13 minutes;
the embodiment also provides a method for preparing the liquid alkali-free accelerator by using the stabilizer, which comprises the following steps:
adding 250g of water into a reaction kettle, adding 150g of a stabilizer for a liquid alkali-free setting accelerator, and stirring for 10 minutes; then 600g of aluminum sulfate octadecahydrate is slowly added into the reaction kettle, and the mixture is continuously stirred until the aluminum sulfate octadecahydrate is completely dissolved, so that the liquid alkali-free accelerator is obtained.
Experimental example 1
The liquid alkali-free accelerator product prepared in the embodiment is detected by using standard portland cement according to the GB/T35159-2017 requirements, and the doping amount is 7%. The detection results are shown in table 1:
table 1 test results of examples
Tests show that simple equipment and simple processes can be adopted by using the stabilizer for the liquid alkali-free accelerator to prepare the environment-friendly liquid alkali-free accelerator which meets the national standard and is convenient for construction.
Experimental example 2
The accelerating agent prepared in the example was observed to have delamination, crystallization or precipitation after being aged at 5 ℃, 20 ℃, 30 ℃ and 35 ℃, and the following example was used as a control group:
control group 1
On the basis of example 3, the difference lies in: diethanolamine, an organic complexing agent, is not added;
control group 2
On the basis of example 3, the difference lies in: polyaspartic acid without a polymeric dispersant;
control group 3
On the basis of example 3, the difference lies in: replacing polyethylene wax with industrial-grade hydroxymethyl cellulose ether;
control group 4
On the basis of example 3, the difference lies in: adding 60g of polyethylene wax and 420g of water into a reaction kettle, adding 50g of diethanolamine, 50g of isopropanolamine, 60g of triethanolamine, 10g of polyaspartic acid with the molecular weight of 5000 and 50g of hydroxyethylidene diphosphonic acid into the reaction kettle, starting high-speed dispersion, wherein the linear velocity of the edge of a paddle reaches 18m/s during high-speed dispersion, and obtaining the polyethylene wax after high-speed dispersion for 13 minutes;
control group 5
On the basis of example 3, the difference lies in: 60g of polyethylene wax, 50g of diethanolamine, 50g of isopropanolamine, 60g of triethanolamine, 10g of polyaspartic acid with the molecular weight of 5000, 50g of hydroxyethylidene diphosphonic acid and 420g of water are all added into a reaction kettle, high-speed dispersion is started, the linear velocity of the edge of a paddle reaches 18m/s during high-speed dispersion, and the high-speed dispersion is obtained after 13 minutes;
the results are shown in table 2:
TABLE 2
Through the test, the following results can be seen: the liquid alkali-free accelerator obtained in the examples has better stability and wider adaptive temperature range, and the following results are found in experiments: although macromolecular materials such as cellulose can increase the viscosity of the system, flocculation is more likely to occur, so that the system is more likely to form aggregates to cause flocculation and stratification.
Claims (8)
1. The stabilizer for the liquid alkali-free accelerator is characterized by comprising the following components in percentage by solid content: 3% -9% of thickening thixotropic agent; 20-50% of organic complexing agent, 5-15% of organic early strength agent, less than or equal to 2% of macromolecular dispersing agent, less than or equal to 10% of crystal form regulator and the balance of water.
2. The stabilizer for the liquid alkali-free accelerator according to claim 1, wherein the thickening thixotropic agent is any one or more of fumed silica, organic bentonite, hydrogenated castor oil, polyamide wax and polyethylene wax.
3. The stabilizer for a liquid alkali-free accelerator according to claim 1, wherein the organic complexing agent is diethanolamine.
4. The stabilizer for the liquid alkali-free accelerator according to claim 1, wherein the organic early strength agent is one or a mixture of triethanolamine and isopropanolamine.
5. The stabilizer for a liquid alkali-free accelerator according to claim 1, wherein the polymeric dispersant is: one or more of polyepoxysuccinic acid with molecular weight ranging from 400 to 1500, polyepoxysuccinic acid salt with molecular weight ranging from 400 to 1500 and polyaspartic acid with molecular weight ranging from 1000 to 5000.
6. The stabilizer for liquid alkali-free accelerator according to claim 1, wherein the crystal form modifier is any one or more of aminotrimethylene methylene phosphonic acid, hydroxyethylidene diphosphonic acid and ethylene diamine tetramethylene phosphonic acid.
7. The method for preparing a stabilizer for a liquid alkali-free quick-setting admixture as claimed in any one of claims 1 to 6, comprising the steps of:
1) adding the thickening thixotropic agent and water into a reaction kettle, stirring at low speed for 10-15min, stopping stirring, and soaking for 10-15 min; 2) adding the rest components into a reaction kettle, and stirring at low speed for 10-15min to mix thoroughly; 3) dispersing at high speed for 10-15min to obtain liquid alkali-free accelerator stabilizer; wherein the linear speed of the edge of the paddle reaches 18m/s during high-speed dispersion.
8. The method for preparing a stabilizer for a liquid alkali-free quick-setting admixture as claimed in any one of claims 1 to 6, comprising the steps of: adding the thickening thixotropic agent and water into a reaction kettle, adding other components into the reaction kettle, and stirring until the components are uniform to obtain the liquid alkali-free accelerator stabilizer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010269477.5A CN111454013B (en) | 2020-04-08 | 2020-04-08 | Stabilizer for liquid alkali-free accelerator and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202010269477.5A CN111454013B (en) | 2020-04-08 | 2020-04-08 | Stabilizer for liquid alkali-free accelerator and preparation method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN111454013A true CN111454013A (en) | 2020-07-28 |
CN111454013B CN111454013B (en) | 2022-04-22 |
Family
ID=71674480
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202010269477.5A Active CN111454013B (en) | 2020-04-08 | 2020-04-08 | Stabilizer for liquid alkali-free accelerator and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN111454013B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113185177A (en) * | 2021-05-14 | 2021-07-30 | 山西佳维新材料股份有限公司 | Alkali-free fluorine-free chlorine-free accelerator and preparation method and application thereof |
CN115385597A (en) * | 2022-08-30 | 2022-11-25 | 琼海鑫海混凝土有限公司 | Accelerating agent for sprayed concrete in high-heat area and preparation and use methods thereof |
CN115611545A (en) * | 2022-08-22 | 2023-01-17 | 贵州天威建材科技有限责任公司 | A kind of method that utilizes fluorine silicon slag to prepare dry powder quick-setting agent |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5453123A (en) * | 1992-12-16 | 1995-09-26 | Sika Ag, Vorm. Kaspar Winkler & Co. | Thixotroping and set-accelerating additive for mixtures containing a hydraulic binder, process using the additive, apparatus for preparing the mixtures containing a hydraulic binder as well as the additive |
US20020023574A1 (en) * | 2000-06-21 | 2002-02-28 | Marcel Sommer | Sulfate-free and alkali-free setting and hardening accelerator |
CN106145739A (en) * | 2016-06-27 | 2016-11-23 | 江苏中铁奥莱特新材料股份有限公司 | A kind of environment-friendly type low resilience low-alkali liquid quick-setting agent and preparation method |
CN107915325A (en) * | 2017-12-01 | 2018-04-17 | 李晓强 | Environment protecting scale inhibitor and its manufacture method |
CN108264257A (en) * | 2018-01-08 | 2018-07-10 | 贵州天威建材科技有限责任公司 | A kind of polymer phosphate aluminium series is without chlorine without sulphur alkali-free liquid setting accelerator and preparation method thereof |
CN108585600A (en) * | 2018-05-10 | 2018-09-28 | 宁夏新华轩高新技术有限公司 | A kind of alkali-free liquid accelerator and preparation method thereof |
CN109776015A (en) * | 2019-03-26 | 2019-05-21 | 西安建筑科技大学 | A kind of liquid accelerator and its preparation method and use |
CN110615638A (en) * | 2019-10-15 | 2019-12-27 | 天津冶建特种材料有限公司 | Low-temperature-resistant liquid alkali-free setting accelerator and preparation method thereof |
CN110922085A (en) * | 2019-12-16 | 2020-03-27 | 武汉优城科技有限公司 | Aluminum sulfate supersaturated suspension type alkali-free liquid accelerator and preparation method thereof |
-
2020
- 2020-04-08 CN CN202010269477.5A patent/CN111454013B/en active Active
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5453123A (en) * | 1992-12-16 | 1995-09-26 | Sika Ag, Vorm. Kaspar Winkler & Co. | Thixotroping and set-accelerating additive for mixtures containing a hydraulic binder, process using the additive, apparatus for preparing the mixtures containing a hydraulic binder as well as the additive |
US20020023574A1 (en) * | 2000-06-21 | 2002-02-28 | Marcel Sommer | Sulfate-free and alkali-free setting and hardening accelerator |
CN106145739A (en) * | 2016-06-27 | 2016-11-23 | 江苏中铁奥莱特新材料股份有限公司 | A kind of environment-friendly type low resilience low-alkali liquid quick-setting agent and preparation method |
CN107915325A (en) * | 2017-12-01 | 2018-04-17 | 李晓强 | Environment protecting scale inhibitor and its manufacture method |
CN108264257A (en) * | 2018-01-08 | 2018-07-10 | 贵州天威建材科技有限责任公司 | A kind of polymer phosphate aluminium series is without chlorine without sulphur alkali-free liquid setting accelerator and preparation method thereof |
CN108585600A (en) * | 2018-05-10 | 2018-09-28 | 宁夏新华轩高新技术有限公司 | A kind of alkali-free liquid accelerator and preparation method thereof |
CN109776015A (en) * | 2019-03-26 | 2019-05-21 | 西安建筑科技大学 | A kind of liquid accelerator and its preparation method and use |
CN110615638A (en) * | 2019-10-15 | 2019-12-27 | 天津冶建特种材料有限公司 | Low-temperature-resistant liquid alkali-free setting accelerator and preparation method thereof |
CN110922085A (en) * | 2019-12-16 | 2020-03-27 | 武汉优城科技有限公司 | Aluminum sulfate supersaturated suspension type alkali-free liquid accelerator and preparation method thereof |
Non-Patent Citations (1)
Title |
---|
杨力远等: ""喷射混凝土液体速凝剂研究现状"", 《隧道建设》 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113185177A (en) * | 2021-05-14 | 2021-07-30 | 山西佳维新材料股份有限公司 | Alkali-free fluorine-free chlorine-free accelerator and preparation method and application thereof |
CN115611545A (en) * | 2022-08-22 | 2023-01-17 | 贵州天威建材科技有限责任公司 | A kind of method that utilizes fluorine silicon slag to prepare dry powder quick-setting agent |
CN115611545B (en) * | 2022-08-22 | 2023-12-08 | 贵州天威建材科技有限责任公司 | Method for preparing dry powder accelerator by utilizing fluorosilicone residues |
CN115385597A (en) * | 2022-08-30 | 2022-11-25 | 琼海鑫海混凝土有限公司 | Accelerating agent for sprayed concrete in high-heat area and preparation and use methods thereof |
CN115385597B (en) * | 2022-08-30 | 2023-07-18 | 琼海鑫海混凝土有限公司 | Accelerating agent for sprayed concrete in high-heat area and preparation and use methods thereof |
Also Published As
Publication number | Publication date |
---|---|
CN111454013B (en) | 2022-04-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN111454013B (en) | Stabilizer for liquid alkali-free accelerator and preparation method thereof | |
CN113603384B (en) | Super-early-strength fluoride-free alkali-free liquid accelerator and preparation method thereof | |
CN111892327B (en) | Liquid alkali-free accelerator and preparation method thereof | |
CN114014582B (en) | Chlorine-free, fluorine-free and alkali-free liquid accelerator and preparation method and application thereof | |
CN111333362A (en) | Low-dosage high-early-strength alkali-free liquid accelerator and preparation method thereof | |
CN113135689A (en) | Elasticity-reducing low-sulfur alkali-free liquid accelerator and preparation method thereof | |
CN110451838A (en) | A kind of novel energy-saving environment-friendly alkali-free quick-coagulant and preparation method thereof | |
CN107459278A (en) | A kind of gunite concrete low-alkali liquid quick-setting agent and preparation method thereof | |
CN115353317B (en) | High-aluminum-content accelerator and preparation method thereof | |
CN113698124A (en) | Alkali-free liquid accelerator and preparation method thereof | |
CN114735961B (en) | Solid-liquid dual-purpose alkali-free accelerator and preparation method and application thereof | |
CN111056762B (en) | Alkali-free liquid accelerator and preparation method thereof | |
CN110218019A (en) | Early high-strength compound alkali-free liquid accelerator, preparation method and gunite concrete | |
CN105541173A (en) | Penetrating type liquid hardening agent and preparation method thereof | |
CN110963732A (en) | Environment-friendly alkali-free liquid accelerator and normal-temperature preparation method thereof | |
CN104987027A (en) | High-speed rail ballastless track concrete roadbed slab crack restoration material and preparation and application thereof | |
CN110963741A (en) | Early-strength powdery alkali-free liquid accelerator core master batch and preparation method and application thereof | |
CN116874223A (en) | Powdered alkali-free accelerator and preparation method thereof | |
CN116332555B (en) | Sprayed concrete super-early-strength low-resilience additive, preparation method thereof and concrete | |
CN111153619B (en) | Non-hazardous chemical substance alkali-free accelerator of magnesium aluminum fluoride system and preparation method thereof | |
CN113429149A (en) | High early strength alkali-free liquid accelerator and preparation method thereof | |
CN105503016B (en) | A kind of high-strength is without sulphur alkali-free liquid accelerator and preparation method thereof | |
CN109761532B (en) | Low-resilience high-early-strength alkali-free liquid accelerator and preparation method thereof | |
CN112225486B (en) | Stable alkali-free liquid accelerator and preparation method and application thereof | |
CN115611545B (en) | Method for preparing dry powder accelerator by utilizing fluorosilicone residues |
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 | ||
GR01 | Patent grant | ||
GR01 | Patent grant |