Nothing Special   »   [go: up one dir, main page]

CN101659527B - Modified aluminate low-alkali liquid quick-setting agent - Google Patents

Modified aluminate low-alkali liquid quick-setting agent Download PDF

Info

Publication number
CN101659527B
CN101659527B CN2009101834283A CN200910183428A CN101659527B CN 101659527 B CN101659527 B CN 101659527B CN 2009101834283 A CN2009101834283 A CN 2009101834283A CN 200910183428 A CN200910183428 A CN 200910183428A CN 101659527 B CN101659527 B CN 101659527B
Authority
CN
China
Prior art keywords
alkali metal
water
aluminate
setting agent
properties
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.)
Active
Application number
CN2009101834283A
Other languages
Chinese (zh)
Other versions
CN101659527A (en
Inventor
张建纲
缪昌文
刘加平
冉千平
周伟玲
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangxi Subote New Material Technology Co ltd
Original Assignee
Jiangsu Bote New Materials Co Ltd
Jiangsu Research Institute of Building Science Co Ltd
China Huashi Enterprises Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Jiangsu Bote New Materials Co Ltd, Jiangsu Research Institute of Building Science Co Ltd, China Huashi Enterprises Co Ltd filed Critical Jiangsu Bote New Materials Co Ltd
Priority to CN2009101834283A priority Critical patent/CN101659527B/en
Publication of CN101659527A publication Critical patent/CN101659527A/en
Application granted granted Critical
Publication of CN101659527B publication Critical patent/CN101659527B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Curing Cements, Concrete, And Artificial Stone (AREA)

Abstract

The invention relates to a modified aluminate low-alkali liquid quick-setting agent which is prepared by adopting the following steps: 1) preparing a modifier: preparing the modifier by the following raw materials according to the proportion by weight: 10-40% of silicate, 5-20% of carbonate and the balance of water; 2) preparing alkali metal aluminate solution as follows: preparing the alkali metal aluminate solution by the following raw materials according to the proportion: 20-35% of alkali metal hydroxide, 30-45% of aluminum hydroxide and the balance of water; and 3) preparing the quick-setting agent: adding the modifier prepared in the step 1) into the alkali metal aluminate solution prepared in the step 2) by the dripping way, and carrying out shear mixing, wherein, the proportion by weight of the modifier to the aluminate solution is 1:5.5-1:7, water needs to be added while dripping for dissolving a formed gel, and the adding amount of the water is 3.4-6 times of the weight of the modifier. The liquid quick-setting agent disclosed by the invention can particularly shorten the interval between initial setting time and final setting time, thereby having good adaptability to a variety of cement and being widely used in sprayed concrete construction.

Description

A kind of modified aluminate low-alkali liquid quick-setting agent
Technical field
The present invention relates to a kind of liquid accelerator that is used for sprayed concrete and mortar, this accelerating chemicals can be widely used in the construction of shotcrete of underground engineering constructions such as tunnel, mine, underground power house.
Background technology
Sprayed concrete has lot of superiority in underground construction and rock support, become extremely important and necessary measure in the modern underground works.Along with the development of wet-mix shotcrete technology, expanded the use range of sprayed concrete in underground works greatly.The most important effect of liquid accelerator for sprayed concrete is to accelerate condensing of concrete mix, improves early strength, can increase a jetting thickness like this and shortens and spray the pitch time of one deck down.
Liquid accelerator join in the sprayed concrete with cement in mineral hydration reaction fast takes place, cement is condensed at short notice, early strength increases rapidly.The action effect of accelerating chemicals and the mineral constituent in the cement and content have confidential relation, yet are subjected to all multifactor influences such as starting material, production technique, mineral composition obvious difference in the different cement.In China, can contain in the ordinary Portland cement and be not more than 20% nonactive adulterant, and the numerous cement adaptability of liquid accelerator that causes of adulterant kind is very outstanding, influences its use in sprayed concrete.
Traditional Liquid Aluminate Accelerating Additive component is single, mainly makes cement setting by the aquation that promotes the aluminium mineral material in the cement.Yet for the more cement of mineral admixture, because tricalcium aluminate content is relatively low, its short effect of coagulating is difficult to satisfy relevant requirement, therefore shows as inferior suitability, and range of application is restricted.In addition, aluminate accelerating chemicals alkali content (Na 2O+0.658K 2O) very high, generally greater than 15%, cause alkali-aggregate reaction easily, influence project durability.Reported a kind of liquid accelerator that is prepared from by potassium aluminate, salt of wormwood as U.S. Pat 4504345, this product alkali content surpasses 20%, and prices of raw and semifnished materials costlinesses such as potassium hydroxide, salt of wormwood, is unfavorable for that large-scale promotion uses.
Summary of the invention
The purpose of this invention is to provide a kind of modified aluminate liquid accelerator that can overcome above-mentioned technological deficiency, this liquid accelerator has short, characteristics such as alkali content is lower, cement adaptability is good time of coagulation.
In the aluminum oxide preparation field, the solution that contains silicate, carbonate aluminate can reduce the crystallization velocity of aluminium hydroxide, suppresses the hydrolysis reaction of aluminate solution, improves the stability of solution.This mainly is owing to silicate, carbonate can change the kenel of aluminium element in solution, exists network-like macroanion and Al-O-H that Al-O-Al is connected with Al-O-Si and Si-O-Si key in the siliceous sodium aluminate solution ... the Al hydrogen bond structure.And along with Al 2O 3And SiO 2Concentration increase network-like negatively charged ion and become many, become greatly, so the silicon-aluminum containing acid sodium solution is inorganic polymer solution rather than the supersaturated sodium aluminate solution thought in the past.And in the chemistry of cement field, Al-O-Si and Si-O-Si have very high reactive behavior, can chemical reaction take place rapidly with the mineral in the cement, thereby promote the aquation of cement.
The applicant finds after deliberation: compare with single aluminate accelerating chemicals, liquid sodium aluminate through persilicate, carbonate modification has the fabulous short performance of coagulating for cement slurry, especially can shorten the pitch time of initial set and final set, this characteristic is for improving the bonding very favourable of sprayed concrete and rock.This may be since silicate, the carbonate of introducing more help with cement slurry in mineral generation hydration reactions such as calcium hydroxide, tricalcium silicate, and traditional aluminate accelerating chemicals is just consuming gypsum, is promoting aspect such as aluminate aquation to play a major role.Help preventing aluminate generation hydrolysis reaction through the network molecular structure in the aluminate solution of modification simultaneously, can improve the package stability of liquid accelerator.
The applicant also finds after deliberation: the direct mixing with aluminate solution of the aqueous solution of silicate, carbonate can not be obtained stable solution system, in the blended process, because the variation of local silicon aluminum ratio, pH value can form gel, this gel is difficult to dissolving under the alr mode of routine.Yet, under the high-shear stirring condition, aluminate solution being joined in the mixing solutions of silicate, sodium aluminate in the mode that drips, formed at the beginning small amount of gel can be dissolved gradually, obtains clear soln again.
Above-mentioned high-shear agitation condition is the well-known technical qualification of a kind of chemical field, and available common mixing machine, homogenizer are realized.The basic definition of fluid shearing speed is velocity slope dv/dy, and its unit is the inverse (S of time -1).
Based on above-mentioned research, the applicant proposes a kind of modified aluminate liquid accelerator, and this accelerating chemicals is prepared from by the following step:
1) preparation of properties-correcting agent
This properties-correcting agent is prepared from by weight proportion by following starting material: silicate, 10~40%; Carbonate, 5~20%; All the other are water;
2) preparation of alkali metal aluminate solution
This alkali metal aluminate solution is prepared from by following proportion of raw material: alkali metal hydroxide, 20~35%; Aluminium hydroxide, 30~45%; All the other are water;
3) allotment of accelerating chemicals
The properties-correcting agent that step 1) is made joins step 2 in the mode that drips) alkali metal aluminate solution that makes, and carry out high-shear and stir; The mass ratio of properties-correcting agent and aluminate solution is: 1: 5.5~1: 7; A spot of gel can appear in the starting stage that properties-correcting agent drips, and adds portion water and can quicken the agglomerative dissolving, and the add-on of water is 3.4~6 times of properties-correcting agent quality.
In the step 1), at first with dissolves carbonate in water, and then the heating condition under silicate is joined in the carbonate solution, form transparent solution.Optionally the silicates material is water glass, Starso or liquid soluble glass, preferred water glass.Optionally carbonate is yellow soda ash, salt of wormwood, preferred yellow soda ash.Heating temperature is 50~80 ℃, preferred 55~70 ℃.
Step 2) in, at first alkali metal hydroxide is dissolved in the water, under the condition of heating aluminium hydroxide is added wherein then, Heating temperature is 80~130 ℃, preferred 100~130 ℃.Reaction times is 2~8 hours, preferred 3~5 hours.Reaction vessel is a reactor of taking back the stream device.
Above-mentioned aluminium hydroxide is general industry aluminium hydroxide, preferred Al 2O 3>63.5%, water ratio is less than 5% aluminium hydroxide.Selected alkali metal hydroxide is the alkali metal hydroxide of solubility, comprises sodium hydroxide, potassium hydroxide, preferred sodium hydroxide.
In the step 3), at first alkali metal aluminate is joined in the reactor, start high-shear mixer, stirring velocity is greater than 1000S -1, then properties-correcting agent is added drop-wise in the reactor.The initial stage that properties-correcting agent drips gel can occur in the solution, and add the water of part this moment, and gel can dissolve gradually.Be added dropwise to complete the back and continued stirring reaction 30~120 minutes, form transparent and uniform solution and be low-alkaline liquid accelerating agent of the present invention.The whole process need of reaction carries out preferred 10~30 ℃ being lower than under 40 ℃ the temperature.The length that the dropping time of properties-correcting agent will try one's best, in order to avoid the gel that forms is difficult to dissolving, reasonably the dropping time is 20~60 minutes, preferred 30~50 minutes.
The present invention has following positive effect:
1, according to the experiment condition of JC477-2005 " sprayed concrete accelerating chemicals ", patent of the present invention promptly can make cement initial set within 4 minutes, final set within 10 minutes at (2%~5%) under the lower volume.
2, according to the test conditions of JC477-2005 " sprayed concrete accelerating chemicals ", more than 10Mpa, the intensity storage rate was greater than 80% in 28 days in the 1 day intensity that can make sand-cement slurry for patent of the present invention.
3, patent of the present invention provided contains silicate, carbonate low-alkali liquid quick-setting agent, has no irritating odor, and can bring good working environment, has good preservation stability under-5~35 ℃ temperature.
Embodiment
Following example more detailed description the preparation process of modified aluminate low-alkali liquid quick-setting agent of the present invention, but these examples never limit this scope of invention, if not separately in the following example of explanation the umber of quality all refer to mass parts.
Embodiment 1.
(1) preparation of aluminate properties-correcting agent
13.6 parts of yellow soda ash are dissolved in 59.2 parts of water, are heated to 60 ℃, add 27.2 parts of water glass, form transparent solution, obtain properties-correcting agent.
(2) preparation of alkali metal aluminate solution
In 35 parts of dissolution of sodium hydroxide to 30 part water, be heated to 120 ℃, add 45 parts of aluminium hydroxides, reaction 4h obtains alkali metal aluminate solution.
(3) preparation of accelerating chemicals
Above-mentioned aluminate solution is joined in the there-necked flask for 240 parts, open high-shear and stir, 40 parts of properties-correcting agent are joined in the dropping funnel, the dropping time was controlled at about 20 minutes.When gel occurring, 220 parts of water are joined in the flask.Be added dropwise to complete the back and continue reaction 1 hour.The clear solution of Xing Chenging is modified aluminate low-alkali liquid quick-setting agent at last.
Embodiment 2.
(1) preparation of aluminate properties-correcting agent
20 parts of yellow soda ash are added in 29 parts of water, be heated to 70 ℃, add 40 inclined to one side parts of water glass, form transparent solution, obtain properties-correcting agent.
(2) preparation of alkali metal aluminate solution
In 20 parts of dissolution of sodium hydroxide to 50 part water, be heated to 120 ℃, add 30 parts of aluminium hydroxides, reaction 3.5h obtains alkali metal aluminate solution.
(3) preparation of accelerating chemicals
Above-mentioned aluminate solution is joined in the there-necked flask for 250 parts, open high-shear and stir, 36 parts of properties-correcting agent are joined in the dropping funnel, the dropping time was controlled at about 30 minutes.When gel occurring, 214 parts of water are joined in the flask.Be added dropwise to complete the back and continue reaction 2 hours.The clear solution of Xing Chenging is the modified aluminate liquid accelerator at last.
Embodiment 3
(1) preparation of aluminate properties-correcting agent
5 parts of salt of wormwood are added in 75 parts of water, be heated to 70 ℃, add 20 parts of water glass, form transparent solution, obtain properties-correcting agent.
(2) alkali metal aluminate solution
In 20 parts of dissolution of sodium hydroxide to 54 part water, be heated to 120 ℃, add 26 parts of aluminium hydroxides, reaction 3.5h obtains alkali metal aluminate solution.
(3) preparation of accelerating chemicals
Above-mentioned aluminate solution is joined in the there-necked flask for 280 parts, open high-shear and stir, 50 parts of properties-correcting agent are joined in the dropping funnel, the dropping time was controlled at about 70 minutes.When gel occurring, 170 parts of water are joined in the flask.Be added dropwise to complete the back and continue reaction 1 hour.The clear solution of Xing Chenging is the modified aluminate liquid accelerator at last.
Embodiment 4
(1) preparation of aluminate properties-correcting agent
16 parts of yellow soda ash are added in 75 parts of water, be heated to 70 ℃, add 32 parts of water glass, form transparent solution, obtain properties-correcting agent.
(2) alkali metal aluminate solution
32 parts of potassium hydroxide are dissolved in 33 parts of water, are heated to 120 ℃, add 35 parts of aluminium hydroxides, reaction 3.5h obtains alkali metal aluminate solution.
(3) preparation of accelerating chemicals
Above-mentioned aluminate solution is joined in the there-necked flask for 260 parts, open high-shear and stir, 45 parts of properties-correcting agent are joined in the dropping funnel, the dropping time was controlled at about 45 minutes.When gel occurring, 180 parts of water are joined in the flask.Be added dropwise to complete the back and continue reaction 1 hour.The clear solution of Xing Chenging is the modified aluminate liquid accelerator at last.
Application example 1.
Cement paste test time of coagulation
Lafarge PO.42.5 cement 400
Water 160
Strength of cement mortar
Test Lafarge PO42.5 cement 900
Standard sand 1350
Water 450
Accelerating chemicals added in the cement slurry according to 3% of cement weight, and above-mentioned water consumption has comprised water contained in the liquid accelerator simultaneously.In the strength test, except testing 1 day intensity and 28 days intensity, do not carried out strength trial, be mixed with the mortar of accelerating chemicals and the ratio of its 28 days intensity in order to test to adding the blank mortar of any quick-hardening.Carried out the test of cement paste time of coagulation and mortar strength simultaneously with commercially available Liquid Aluminate Accelerating Additive.Test-results such as table 1 and table 2.
The effect of table 1. accelerating chemicals (I)
Figure G2009101834283D00061
The effect of table 2. accelerating chemicals (II)
Figure G2009101834283D00062
Use the modified aluminate low-alkali liquid quick-setting agent cement paste than aluminate accelerating chemicals certain shortening to be arranged time of coagulation as can be seen from table 1 and table 2, the interval of initial set and final setting time is shortened then more obvious; In addition, 28 days strength ratios of the mortar of liquid accelerator of the present invention and Liquid Aluminate Accelerating Additive also are significantly improved.
Application example 2
Carried out simultaneous test for the relatively poor several cement of conventional aluminium Barbiturates accelerating chemicals adaptability, test method is with example 1, and Comparative Examples is selected commercially available Liquid Aluminate Accelerating Additive, test-results such as table 3
Table 3. simultaneous test
Figure G2009101834283D00071
As seen, modified aluminate low-alkali liquid quick-setting agent provided by the invention has better cement adaptability than traditional aluminate class accelerating chemicals.

Claims (8)

1. modified aluminate low-alkali liquid quick-setting agent is characterized in that adopting following steps to be prepared from:
1) preparation of properties-correcting agent
This properties-correcting agent is prepared from by weight proportion by following starting material: silicate, 10~40%; Carbonate, 5~20%; All the other are water; Its concrete preparation process is: at first with dissolves carbonate in water, be heated to 50~80 ℃, again silicate is joined in the carbonate solution, form transparent solution; Aforementioned silicate is selected from water glass, Starso or liquid soluble glass; Carbonate is selected from yellow soda ash or salt of wormwood;
2) preparation of alkali metal aluminate solution
This alkali metal aluminate solution is prepared from by following proportion of raw material: alkali metal hydroxide, 20~35%; Aluminium hydroxide, 30~45%; All the other are water;
3) allotment of accelerating chemicals
The properties-correcting agent that step 1) is made joins step 2 in the mode that drips) alkali metal aluminate solution that makes, and carry out shear agitation; The mass ratio of properties-correcting agent and aluminate solution is: 1: 5.5~1: 7; Need add entry during dropping, make the gel dissolving of formation, the add-on of water is 3.4~6 times of properties-correcting agent weight, and its concrete allocation process is:
At first alkali metal aluminate is joined in the reactor, greater than 1000S -1Shear conditions under react, when gel occurring in the solution, when dripping properties-correcting agent, add water; Be added dropwise to complete the back and continued stirring reaction 30~120 minutes, promptly make finished product.
2. modified aluminate low-alkali liquid quick-setting agent according to claim 1 is characterized in that being heated in the step 1) 55~70 ℃.
3. modified aluminate low-alkali liquid quick-setting agent according to claim 1 is characterized in that step 2) at first alkali metal hydroxide is dissolved in the water, be heated to 80~150 ℃ then, again aluminium hydroxide is added wherein, reacted 2~8 hours.
4. as modified aluminate low-alkali liquid quick-setting agent as described in the claim 3, it is characterized in that step 2) in preferred 100~130 ℃ of Heating temperature, preferred 3~5 hours of reaction times.
5. as modified aluminate low-alkali liquid quick-setting agent as described in claim 1 or 3 or 4, it is characterized in that step 2) described in alkali metal hydroxide be the alkali metal hydroxide of solubility, Al in the described aluminium hydroxide 2O 3Content>63.5%.
6. modified aluminate low-alkali liquid quick-setting agent according to claim 1 is characterized in that dripping in the step 3) preferred 30~50 minutes of time of properties-correcting agent.
7. as modified aluminate low-alkali liquid quick-setting agent as described in claim 1 or 6, the whole dropwise reaction process that it is characterized in that step 3) is carried out being lower than under 40 ℃ the temperature.
8. as modified aluminate low-alkali liquid quick-setting agent as described in claim 1 or 6, it is characterized in that preferred 10~30 ℃ of the drip reacting temperature of step 3).
CN2009101834283A 2009-09-21 2009-09-21 Modified aluminate low-alkali liquid quick-setting agent Active CN101659527B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2009101834283A CN101659527B (en) 2009-09-21 2009-09-21 Modified aluminate low-alkali liquid quick-setting agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2009101834283A CN101659527B (en) 2009-09-21 2009-09-21 Modified aluminate low-alkali liquid quick-setting agent

Publications (2)

Publication Number Publication Date
CN101659527A CN101659527A (en) 2010-03-03
CN101659527B true CN101659527B (en) 2011-08-17

Family

ID=41787811

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2009101834283A Active CN101659527B (en) 2009-09-21 2009-09-21 Modified aluminate low-alkali liquid quick-setting agent

Country Status (1)

Country Link
CN (1) CN101659527B (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102219423B (en) * 2011-04-20 2013-08-21 安徽中铁工程材料科技有限公司 Method for preparing novel low-alkaline liquid setting accelerator
CN103819122A (en) * 2014-01-24 2014-05-28 江西省交通工程集团公司 Preparation method of low-alkaline liquid setting accelerator for sprayed concrete
CN103819114B (en) * 2014-02-17 2016-01-20 山东大学 The sprayed concrete preparation method of low alkali polymer high efficiency liquid accelerating agent
CN105906225B (en) * 2016-04-14 2017-09-15 湖北腾辰科技股份有限公司 A kind of application of discarded sewage in liquid accelerator synthesis
CN106082750B (en) * 2016-06-02 2017-11-21 石家庄市长安育才建材有限公司 Gunite concrete low resilience liquid accelerator and preparation method thereof
CN106431070B (en) * 2016-09-20 2019-01-01 江苏苏博特新材料股份有限公司 A kind of Al-Zn-Si nano-complex fast coagulating early strength agent and preparation method thereof
CN106746838A (en) * 2016-11-28 2017-05-31 欧阳会幼 A kind of aluminate modified high-efficient liquid accelerator
CN106630725B (en) * 2016-12-01 2020-03-31 江苏苏博特新材料股份有限公司 Liquid accelerator for sprayed concrete and preparation method thereof
CN107512858A (en) * 2017-09-18 2017-12-26 广州速力化工科技有限公司 A kind of cement hardener of functional modification
CN109553325B (en) * 2018-11-15 2021-08-10 江苏博思通新材料有限公司 Preparation method of modified aluminate liquid accelerator

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4504315A (en) * 1983-02-24 1985-03-12 Dynamit Nobel Ag Liquid accelerator for the setting of concrete mixtures
CN1974466A (en) * 2006-12-07 2007-06-06 江苏博特新材料有限公司 Alkali-free liquid setting accelerator for spray concrete
CN101475335A (en) * 2009-01-13 2009-07-08 江苏博特新材料有限公司 Liquid accelerator for sprayed concrete and preparation thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4504315A (en) * 1983-02-24 1985-03-12 Dynamit Nobel Ag Liquid accelerator for the setting of concrete mixtures
CN1974466A (en) * 2006-12-07 2007-06-06 江苏博特新材料有限公司 Alkali-free liquid setting accelerator for spray concrete
CN101475335A (en) * 2009-01-13 2009-07-08 江苏博特新材料有限公司 Liquid accelerator for sprayed concrete and preparation thereof

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
JP特开2007-145652A 2007.06.14
周伟玲 等.液体无碱速凝剂的制备与应用技术研究.《混凝土与水泥制品》.2009,(第3期),第6-8页. *

Also Published As

Publication number Publication date
CN101659527A (en) 2010-03-03

Similar Documents

Publication Publication Date Title
CN101659527B (en) Modified aluminate low-alkali liquid quick-setting agent
CN101665336B (en) Preparation method of low-alkaline liquid accelerating agent
CN104446090B (en) A kind of alkali-free liquid accelerator of durability and preparation method thereof
CN104193212B (en) Sprayed concrete low resilience low-alkali liquid quick-setting agent and preparation method thereof
CN109678388A (en) A kind of antifreeze alkali-free liquid accelerating agent and preparation method thereof
CN105384377A (en) Accelerator auxiliary material based on composite polymerized flocculating agent and preparation method thereof
CN108996975A (en) A kind of subzero temperature steel bar sleeve for connection grouting material and preparation method thereof
CN104781209A (en) Geopolymer composition comprising additives
CN102219423B (en) Method for preparing novel low-alkaline liquid setting accelerator
CN106946513B (en) A kind of normal temperature solidified geopolymer and its application
CN108585587A (en) A kind of room temperature synthesis early-strength alkali-free liquid setting accelerator and preparation method thereof
JP2012121804A (en) Setting and hardening accelerator for hydraulic binder, usage and producing method of the same
CN108164179A (en) A kind of cement concrete antifreezer suitable for ultra-low temperature surroundings
CN101143775B (en) Large adulteration quantity fly ash gel material for building mortar and preparation method thereof
CA3009532C (en) Accelerator for hydraulic composition
CN109336506A (en) A kind of curing agent and its application method with relatively strongization ability
CN110357480A (en) Low alkali accelerator of a kind of gunite concrete polymer and preparation method thereof
CN112441765B (en) Alkali activator, alkali-activated gel material, concrete and preparation method of concrete
CN110128081A (en) A kind of concrete and preparation method thereof
CN100422106C (en) Accelerator for hydraulic binder
CN112159130A (en) Geopolymer cementing material for temporary spray anchor support engineering and preparation method thereof
CN104230266A (en) High-strength dry-mixed mortar stirring method
CN103204645A (en) High-strength environmental-friendly high-efficiency water reducing admixture and preparation method thereof
CN103265238A (en) Modified cement-water glass slurry and application method thereof
CN108793923B (en) Improved gypsum plastering mortar and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
ASS Succession or assignment of patent right

Owner name: JAINGSU ACADEMY OF BUILDING RESEARCH CO., LTD. CHI

Free format text: FORMER OWNER: JAINGSU ACADEMY OF BUILDING RESEARCH CO., LTD.

C41 Transfer of patent application or patent right or utility model
TA01 Transfer of patent application right

Effective date of registration: 20110616

Address after: 211103, No. 59 West Wan An Road, Jiangning District, Jiangsu, Nanjing

Applicant after: JIANGSU BOTE NEW MATERIALS Co.,Ltd.

Co-applicant after: JIANGSU RESEARCH INSTITUTE OF BUILDING SCIENCE Co.,Ltd.

Co-applicant after: CHINA HUASHI ENTERPRISES Co.,Ltd.

Address before: 211103, No. 59 West Wan An Road, Jiangning District, Jiangsu, Nanjing

Applicant before: JIANGSU BOTE NEW MATERIALS Co.,Ltd.

Co-applicant before: JIANGSU RESEARCH INSTITUTE OF BUILDING SCIENCE Co.,Ltd.

C14 Grant of patent or utility model
GR01 Patent grant
ASS Succession or assignment of patent right

Owner name: JIANGSU SUBOTE NEW MATERIAL CO., LTD.

Free format text: FORMER OWNER: BOTE NEW MATERIAL CO., LTD., JIANGSU

Effective date: 20140529

Free format text: FORMER OWNER: JAINGSU ACADEMY OF BUILDING RESEARCH CO., LTD. CHINA HUASHI ENTERPRISES COMPANY LIMITED

Effective date: 20140529

C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20140529

Address after: 211103, No. 59 West Wan An Road, Jiangning District, Jiangsu, Nanjing

Patentee after: SOBUTE NEW MATERIALS Co.,Ltd.

Address before: 211103, No. 59 West Wan An Road, Jiangning District, Jiangsu, Nanjing

Patentee before: JIANGSU BOTE NEW MATERIALS Co.,Ltd.

Patentee before: JIANGSU RESEARCH INSTITUTE OF BUILDING SCIENCE Co.,Ltd.

Patentee before: CHINA HUASHI ENTERPRISES Co.,Ltd.

CP02 Change in the address of a patent holder
CP02 Change in the address of a patent holder

Address after: No.6 shuiyougang, Gulou District, Nanjing City, Jiangsu Province 210013

Patentee after: SOBUTE NEW MATERIALS Co.,Ltd.

Address before: 211103, No. 59 West Wan An Road, Jiangning District, Jiangsu, Nanjing

Patentee before: SOBUTE NEW MATERIALS Co.,Ltd.

TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20231025

Address after: 537100 southwest of the intersection of Ganhua Jinger road and Ganhua Avenue, new material science and Technology Park, Sanli Town, qintang District, Guigang City, Guangxi Zhuang Autonomous Region

Patentee after: Guangxi subote New Material Technology Co.,Ltd.

Address before: No.6 shuiyougang, Gulou District, Nanjing City, Jiangsu Province 210013

Patentee before: SOBUTE NEW MATERIALS Co.,Ltd.