CN113666655A - Material for promoting geopolymer molding in high-humidity environment and preparation method thereof - Google Patents

Material for promoting geopolymer molding in high-humidity environment and preparation method thereof Download PDF

Info

Publication number
CN113666655A
CN113666655A CN202110885741.2A CN202110885741A CN113666655A CN 113666655 A CN113666655 A CN 113666655A CN 202110885741 A CN202110885741 A CN 202110885741A CN 113666655 A CN113666655 A CN 113666655A
Authority
CN
China
Prior art keywords
water
sodium hydroxide
calculated
solid waste
excitant
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202110885741.2A
Other languages
Chinese (zh)
Inventor
王新富
赵恒�
吴求刚
王彦君
周晓芳
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.)
Sinochem Jiangsu Geology And Mineral Resources Design And Research Institute Co ltd
Original Assignee
Sinochem Jiangsu Geology And Mineral Resources Design And Research Institute 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 Sinochem Jiangsu Geology And Mineral Resources Design And Research Institute Co ltd filed Critical Sinochem Jiangsu Geology And Mineral Resources Design And Research Institute Co ltd
Priority to CN202110885741.2A priority Critical patent/CN113666655A/en
Publication of CN113666655A publication Critical patent/CN113666655A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B12/00Cements not provided for in groups C04B7/00 - C04B11/00
    • C04B12/005Geopolymer cements, e.g. reaction products of aluminosilicates with alkali metal hydroxides or silicates
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B18/00Use of agglomerated or waste materials or refuse as fillers for mortars, concrete or artificial stone; Treatment of agglomerated or waste materials or refuse, specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B18/04Waste materials; Refuse
    • C04B18/06Combustion residues, e.g. purification products of smoke, fumes or exhaust gases
    • C04B18/08Flue dust, i.e. fly ash
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B18/00Use of agglomerated or waste materials or refuse as fillers for mortars, concrete or artificial stone; Treatment of agglomerated or waste materials or refuse, specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B18/04Waste materials; Refuse
    • C04B18/14Waste materials; Refuse from metallurgical processes
    • C04B18/141Slags
    • C04B18/145Phosphorus slags
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/006Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing mineral polymers, e.g. geopolymers of the Davidovits type
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00724Uses not provided for elsewhere in C04B2111/00 in mining operations, e.g. for backfilling; in making tunnels or galleries
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/70Grouts, e.g. injection mixtures for cables for prestressed concrete
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P40/00Technologies relating to the processing of minerals
    • Y02P40/10Production of cement, e.g. improving or optimising the production methods; Cement grinding
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/91Use of waste materials as fillers for mortars or concrete

Abstract

The invention discloses a material for promoting geopolymer molding in a high-humidity environment and a preparation method thereof, wherein the raw materials comprise solid waste, an exciting agent, an additive and water; the solid waste is industrial solid waste and comprises fly ash and phosphorus tailing sand; the excitant is an alkaline excitant and is one of a sodium hydroxide excitant, a sodium hydroxide-silica fume composite excitant and a water glass excitant; the additive is xanthan gum, and the addition amount of the additive is 1% of that of the solid waste; the mass ratio (water-solid ratio) of water to solid waste is 0.5-0.75. The invention improves the feasibility of manufacturing the geopolymer grouting filling material by the solid waste, solves the problem that the goaf grouting filling material is difficult to form in the actual grouting process, improves the forming degree of the geopolymer in a high-humidity environment, shortens the final setting time, can consume the industrial solid waste, and simultaneously carries out goaf repair and treatment. The raw material of the invention is industrial solid waste, the price is low, and the source is wide.

Description

Material for promoting geopolymer molding in high-humidity environment and preparation method thereof
Technical Field
The invention relates to the technical field of geopolymer preparation and application, in particular to a material for promoting geopolymer molding in a high-humidity environment and a preparation method thereof.
Background
The geopolymer is a three-dimensional network polymeric gelled material which is formed by mineral condensation polymerization under high alkaline conditions and consists of silicon-oxygen tetrahedron and aluminum-oxygen tetrahedron by using natural minerals or solid wastes and artificial silicon-aluminum compounds as raw materials. Compared with portland cement, geopolymer has the advantages of rich material source, simple preparation process, low production power consumption, low three waste discharge, high strength, high durability, easily available raw materials, low cost, etc. Therefore, in recent years, relevant scholars at home and abroad develop a series of researches on the application of geopolymer to goaf filling and grouting materials. The geopolymer prepared by the solid wastes such as the fly ash, the coal gangue and the like is often used for goaf treatment, so that the goaf activation problem is solved, and a large amount of mine solid wastes are digested. With the continuous and deep research and application of geopolymer preparation technology, geopolymers become hot spots for researching novel green cementing materials at home and abroad by virtue of excellent preparation and cementing properties, and the geopolymers are used for preparing grouting materials to replace cement in the traditional grouting materials, so that the geopolymers have great development prospects.
However, in the practical application process, the goaf environment is found to be special, a large amount of old goaf water exists, the overall goaf humidity is high, and the temperature is low. Therefore, in the actual test process, the geopolymer grouting material has the problem of poor forming in a low-temperature and high-humidity environment, and the test block still has the phenomenon of softness and dryness after being cured in a curing box under simulated conditions (25 ℃, 98 +/-1 percent of humidity) for 28 days. With the intensive research of the polymer grouting material, the factors influencing the formation of geopolymers, such as water-solid ratio, temperature, alkali concentration and modulus of an alkali activator, are found.
Disclosure of Invention
The present invention has been made to overcome the above problems and an object of the present invention is to provide a material for promoting polymer molding in a high-humidity environment and a method for producing the same. In order to achieve the purpose, the invention adopts the following technical scheme:
a material for promoting the formation of geopolymers in high-humidity environment is prepared from solid waste, exciting agent, additive and water;
the solid waste is industrial solid waste and comprises fly ash and phosphorus tailing sand;
the excitant is an alkaline excitant and is one of a sodium hydroxide excitant, a sodium hydroxide-silica fume composite excitant and a water glass excitant;
the additive is xanthan gum, and the addition amount of the additive is 1% of that of the solid waste;
the mass ratio (water-solid ratio) of the water to the solid waste is 0.5-0.75.
The invention also discloses a preparation method of the material for promoting the formation of the geopolymer in the high-humidity environment, which comprises the following steps:
s1, drying the fly ash and the phosphorus tailing sand at 105 ℃ for 12 hours, and cooling, crushing and grinding the dried solid waste raw materials to 200 meshes;
s2, weighing industrial solid wastes such as coal ash, phosphorus tailing sand and the like in a mass ratio of 1:1 to serve as mixed aggregates of the geopolymer;
s3, preparing an exciting agent;
s4, mixing the prepared excitant with the pulverized coal ash and the phosphorus tailing sand (200 meshes) which are dried and ground, adding 1 wt% of xanthan gum geopolymer additive, uniformly mixing and stirring for 10min, injection molding after stirring, and curing and forming in a high-humidity environment (25 ℃, 98 +/-1% of humidity).
As an improvement, when the sodium hydroxide is used as an activator, the sodium hydroxide activator contains water and sodium hydroxide (Na is used)2Calculated as O) is 20 to 25.
As an improvement, when the sodium hydroxide-silica fume is used as an excitantWater and sodium hydroxide (as Na)2O) is 20-25, and silica fume (calculated as SiO)2Calculated as Na) and sodium hydroxide (calculated as Na)2Calculated as O) is 2.
As an improvement, when the water glass is used as an excitant, the water and sodium hydroxide (Na is used)2Calculated by O) is 20-25, and the modulus of the water glass is 2.
As an improvement, the method for preparing the sodium hydroxide excitant in the S3 comprises the following steps: determining the addition amount of mixed aggregate, determining the addition amount of water in the activator according to the water-solid ratio, and determining the addition amount of water and sodium hydroxide (as Na) according to the water and sodium hydroxide2O) of the activator, water and sodium hydroxide (as Na)2Calculated as O) is 20 to 25.
As an improvement, the method for preparing the sodium hydroxide-silica fume excitant in the S3 comprises the following steps: determining the addition amount of mixed aggregate, determining the addition amount of water in the activator according to the water-solid ratio, and determining the addition amount of water and sodium hydroxide (as Na) according to the water and sodium hydroxide2O) is determined, and the addition amount of sodium hydroxide in the exciting agent is determined according to the molar ratio of silica fume (calculated as SiO)2Calculated as Na) and sodium hydroxide (calculated as Na)2O) the amount of silica fume added, water and sodium hydroxide (as Na)2O) is 20-25, and silica fume (calculated as SiO)2Calculated as Na) and sodium hydroxide (calculated as Na)2Calculated as O) is 2.
As an improvement, the method for preparing the sodium hydroxide-silica fume excitant in the S3 comprises the following steps: determining the addition amount of mixed aggregate, determining the addition amount of additional water in the activator according to the modulus and water-solid ratio of water glass, and determining the addition amount of water and sodium hydroxide (as Na)2O) determines the additional amount of sodium hydroxide added to the booster, water and sodium hydroxide (as Na)2Calculated as O) is 20 to 25.
The invention has the advantages that:
1. economic benefits are as follows: the raw material of the invention is industrial solid waste, the price is low, and the source is wide.
2. Environmental protection benefit: the invention not only consumes the storage capacity of a large amount of solid waste, improves the comprehensive utilization amount of the solid waste, reduces the environmental hazard caused by solid waste accumulation, and improves the environmental protection benefit.
3. The practicability is as follows: the invention improves the feasibility of manufacturing the geopolymer grouting filling material by the solid waste, solves the problem that the goaf grouting filling material is difficult to form in the actual grouting process, improves the forming degree of the geopolymer in a high-humidity environment, shortens the final setting time, can consume the industrial solid waste, and simultaneously carries out goaf repair and treatment.
Detailed Description
The present invention will be described in detail and specifically with reference to the following examples so as to facilitate the understanding of the present invention, but the following examples do not limit the scope of the present invention.
Example 1
This example discloses a material for promoting the formation of geopolymers in high humidity environment and a method for preparing the same, and the initial setting and final setting time of geopolymers were measured.
The geopolymer material comprises: fly ash, phosphorus tailings sand, alkali activator and water, wherein the alkali activator is sodium hydroxide, the water-solid ratio is 0.5, and the water and the sodium hydroxide (by Na)2Calculated as O) was 20.
The preparation method of the geopolymer comprises the following steps:
s1, drying the fly ash and the phosphorus tailing sand at 105 ℃ for 12 hours, and removing water;
s2, cooling, crushing and grinding the dried raw materials to 200 meshes, weighing 250g of coal ash and 250g of phosphorus tailing sand respectively, weighing 55.56g of sodium hydroxide, and adding 250g of water to dissolve;
s3, mixing the weighed fly ash, the phosphorus tailings sand and the sodium hydroxide solution, adding 5g of xanthan gum, stirring for 10min, brushing oil on an empty test mold, injecting geopolymer slurry, and vibrating by a vibrating table to eliminate bubbles remained in the polymer so as to ensure the compactness of geopolymer filling, and putting the geopolymer into a curing box for curing, wherein the curing condition of the curing box is as follows: the temperature is 21 ℃ and the relative humidity is 98 +/-1%. And after 3d, removing the mold, and continuously putting the obtained geopolymer test block into a curing box for curing to 28d, wherein the final setting time of the geopolymer test block is measured.
Example 2
This example discloses a material for promoting the formation of geopolymers in high humidity environment and a method for preparing the same, and the initial setting and final setting time of geopolymers were measured.
The geopolymer material comprises: fly ash, phosphorus tailings sand, alkali activator and water, wherein the alkali activator is sodium hydroxide and silica fume, the water-solid ratio is 0.5, and the water and the sodium hydroxide (by Na)2O) was 25, silica fume (in SiO)2Calculated as Na) and sodium hydroxide (calculated as Na)2Calculated as O) is 2.
The preparation method of the geopolymer comprises the following steps:
s1, drying the fly ash and the phosphorus tailing sand at 105 ℃ for 12 hours, and removing water;
s2, cooling, crushing and grinding the dried raw materials to 200 meshes, and weighing 250g of coal ash and phosphorus tailing sand respectively;
s3, weighing 44.44g of sodium hydroxide and 66.67g of silica fume, adding 250g of water for dissolving, and heating and dissolving at 75 ℃ to prepare a composite exciting agent;
s4, mixing the weighed fly ash, the phosphorus tailing sand and the composite activator, adding 5g of xanthan gum, stirring for 10min, brushing oil on an empty test mold, injecting geopolymer slurry, and vibrating by a vibrating table to eliminate bubbles remained in the polymer so as to ensure the compactness of geopolymer filling, and putting the mixture into a curing box for curing, wherein the curing conditions of the curing box are as follows: the temperature is 21 ℃ and the relative humidity is 98 +/-1%. And after 3d, removing the mold, and continuously putting the obtained geopolymer test block into a curing box for curing to 28d, wherein the final setting time of the geopolymer test block is measured.
Example 3
This example discloses a material for promoting the formation of geopolymers in high humidity environment and a method for preparing the same, and the initial setting and final setting time of geopolymers were measured.
The geopolymer material comprises: fly ash, phosphorus tailings sand, alkali activator and water, wherein the original water glass used for preparing the alkali activator is 3.3 modules, the water-solid ratio is 0.5, and water and sodium hydroxide (taking Na as the raw material)2Calculated as O) is 25, and the modulus required for the preparation of the water glass excitant is 2.
The preparation method of the geopolymer comprises the following steps:
s1, drying the fly ash and the phosphorus tailing sand at 105 ℃ for 12 hours, and removing water;
s2, cooling, crushing and grinding the dried raw materials to 200 meshes, and weighing 250g of coal ash and phosphorus tailing sand respectively;
s3, weighing 239.37g of 3.3-mould industrial water glass solution and 17.19g of sodium hydroxide, and adding 96.42g of water to dissolve to prepare an exciting agent;
s4, mixing the weighed fly ash, the phosphorus tailing sand and the exciting agent, adding 5g of xanthan gum, stirring for 10min, brushing oil on an empty test mold, injecting geopolymer slurry, and vibrating by using a vibrating table to eliminate bubbles remained in the polymer so as to ensure the compactness of geopolymer filling, and putting the geopolymer into a curing box for curing, wherein the curing condition of the curing box is as follows: the temperature is 21 ℃ and the relative humidity is 98 +/-1%. And after 3d, removing the mold, and continuously putting the obtained geopolymer test block into a curing box for curing to 28d, wherein the final setting time of the geopolymer test block is measured.
The initial and final set of the geopolymers obtained in examples 1, 2 and 3 were tested, the test methods and the resulting performance data are shown in the following table:
Figure BDA0003194083480000041
according to the above table, the initial and final setting time of the industrial waste geopolymer produced by using the components and the formula provided by the invention is shorter in a normal-temperature high-humidity environment, compared with the existing goaf grouting material, the geopolymer material provided by the invention can be quickly formed under the condition of 98 +/-1%, the forming condition of the geopolymer under high humidity is improved, the overall construction performance is excellent, a wide development prospect is provided for the wide application of the geopolymer in underground engineering, and the geopolymer has a higher practical application value.
The embodiments of the present invention have been described in detail above, but they are merely exemplary, and the present invention is not equivalent to the above described embodiments. Any equivalent modifications and substitutions to those skilled in the art are also within the scope of the present invention. Accordingly, it is intended that all equivalent alterations and modifications be included within the scope of the invention, without departing from the spirit and scope of the invention.

Claims (8)

1. A material for promoting the formation of polymers in a high-humidity environment, characterized in that the raw materials comprise solid waste, an activator, an additive and water;
the solid waste is industrial solid waste and comprises fly ash and phosphorus tailing sand;
the excitant is an alkaline excitant and is one of a sodium hydroxide excitant, a sodium hydroxide-silica fume composite excitant and a water glass excitant;
the additive is xanthan gum, and the addition amount of the additive is 1% of that of the solid waste;
the mass ratio (water-solid ratio) of the water to the solid waste is 0.5-0.75.
2. The material for promoting polymer molding in a high-humidity environment according to claim 1, wherein when said sodium hydroxide is used as an activator, said sodium hydroxide activator contains water and sodium hydroxide (Na) as an activator2Calculated as O) is 20 to 25.
3. The material for promoting polymer molding in a high-humidity environment according to claim 1, wherein said sodium hydroxide-silica fume is used as an activator, and said water and sodium hydroxide (Na) are used as an activator2O) is 20-25, and silica fume (calculated as SiO)2Calculated as Na) and sodium hydroxide (calculated as Na)2Calculated as O) is 2.
4. The material for promoting polymer molding in a high-humidity environment according to claim 1, wherein said water and sodium hydroxide (Na) are added when said water glass is used as an activator2Calculated by O) is 20-25, and the modulus of the water glass is 2.
5. A method for preparing a material for promoting polymer molding in a high-humidity environment according to claim 1, comprising the steps of:
s1, drying the fly ash and the phosphorus tailing sand at 105 ℃ for 12 hours, and cooling, crushing and grinding the dried solid waste raw materials to 200 meshes;
s2, weighing industrial solid wastes such as coal ash, phosphorus tailing sand and the like in a mass ratio of 1:1 to serve as mixed aggregates of the geopolymer;
s3, preparing an exciting agent;
s4, mixing the prepared excitant with the pulverized coal ash and the phosphorus tailing sand (200 meshes) which are dried and ground, adding 1 wt% of xanthan gum geopolymer additive, uniformly mixing and stirring for 10min, injection molding after stirring, and curing and forming in a high-humidity environment (25 ℃, 98 +/-1% of humidity).
6. The material for promoting the formation of geopolymers in high-humidity environment according to claim 5, wherein the method for preparing sodium hydroxide activator in S3 is as follows: determining the addition amount of mixed aggregate, determining the addition amount of water in the activator according to the water-solid ratio, and determining the addition amount of water and sodium hydroxide (as Na) according to the water and sodium hydroxide2O) of the activator, water and sodium hydroxide (as Na)2Calculated as O) is 20 to 25.
7. The material for promoting the formation of geopolymers in high-humidity environment according to claim 5, wherein the method for preparing sodium hydroxide-silica fume excitant in S3 is as follows: determining the addition amount of mixed aggregate, determining the addition amount of water in the activator according to the water-solid ratio, and determining the addition amount of water and sodium hydroxide (as Na) according to the water and sodium hydroxide2O) is determined, and the addition amount of sodium hydroxide in the exciting agent is determined according to the molar ratio of silica fume (calculated as SiO)2Calculated as Na) and sodium hydroxide (calculated as Na)2O) the amount of silica fume added, water and sodium hydroxide (as Na)2O) is 20-25, and silica fume (calculated as SiO)2Calculated as Na) and sodium hydroxide (calculated as Na)2Calculated as O) is 2.
8. According to claim5, the method for preparing the sodium hydroxide-silica fume exciting agent in the S3 is characterized in that: determining the addition amount of mixed aggregate, determining the addition amount of additional water in the activator according to the modulus and water-solid ratio of water glass, and determining the addition amount of water and sodium hydroxide (as Na)2O) determines the additional amount of sodium hydroxide added to the booster, water and sodium hydroxide (as Na)2Calculated as O) is 20 to 25.
CN202110885741.2A 2021-08-03 2021-08-03 Material for promoting geopolymer molding in high-humidity environment and preparation method thereof Pending CN113666655A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110885741.2A CN113666655A (en) 2021-08-03 2021-08-03 Material for promoting geopolymer molding in high-humidity environment and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110885741.2A CN113666655A (en) 2021-08-03 2021-08-03 Material for promoting geopolymer molding in high-humidity environment and preparation method thereof

Publications (1)

Publication Number Publication Date
CN113666655A true CN113666655A (en) 2021-11-19

Family

ID=78541215

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110885741.2A Pending CN113666655A (en) 2021-08-03 2021-08-03 Material for promoting geopolymer molding in high-humidity environment and preparation method thereof

Country Status (1)

Country Link
CN (1) CN113666655A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115477502A (en) * 2022-09-15 2022-12-16 江门市俞嘉科技有限公司 Process for producing water permeable bricks by utilizing solid wastes
CN115818994A (en) * 2022-11-22 2023-03-21 南通河海大学海洋与近海工程研究院 Silica fume base alkali activator and preparation method thereof
CN115893886A (en) * 2022-11-22 2023-04-04 河海大学 Solid waste base-activated cementing material and preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104446045A (en) * 2014-11-05 2015-03-25 武汉理工大学 Alkali-activated cementing material and preparation method thereof
CN108249788A (en) * 2017-12-21 2018-07-06 中国建筑材料科学研究总院有限公司 Alkali-activated carbonatite cementitious material and preparation method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104446045A (en) * 2014-11-05 2015-03-25 武汉理工大学 Alkali-activated cementing material and preparation method thereof
CN108249788A (en) * 2017-12-21 2018-07-06 中国建筑材料科学研究总院有限公司 Alkali-activated carbonatite cementitious material and preparation method thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115477502A (en) * 2022-09-15 2022-12-16 江门市俞嘉科技有限公司 Process for producing water permeable bricks by utilizing solid wastes
CN115818994A (en) * 2022-11-22 2023-03-21 南通河海大学海洋与近海工程研究院 Silica fume base alkali activator and preparation method thereof
CN115893886A (en) * 2022-11-22 2023-04-04 河海大学 Solid waste base-activated cementing material and preparation method thereof
CN115818994B (en) * 2022-11-22 2023-11-21 南通河海大学海洋与近海工程研究院 Silica fume base alkali excitant and preparation method thereof
CN115893886B (en) * 2022-11-22 2024-01-23 河海大学 Solid waste base alkali-activated cementing material and preparation method thereof

Similar Documents

Publication Publication Date Title
CN113666655A (en) Material for promoting geopolymer molding in high-humidity environment and preparation method thereof
CN103232182B (en) Geopolymer/emulsified asphalt composite material and preparation method thereof
CN103214214B (en) Preparation raw materials and preparation method of inorganic man-made rock
CN103880363B (en) A kind of geopolymer/modified waste rubber powder compound material and preparation method thereof
CN110759655B (en) Industrial waste based geopolymer
CN102992717A (en) Preparation method for high-molecular compound-containing metakaolin-based geopolymer cement
CN102910882A (en) Fiber-reinforced alkali-activated cementing material and preparation method thereof
CN113387620B (en) Solidified dredged sludge block based on alkali-activated cementing material and preparation method thereof
CN101913831A (en) Method for producing baking-free bricks by solidifying construction wastes by utilizing phosphogypsum
CN111807782A (en) Fluid-state solidification regeneration mixture, preparation method and application thereof in pit backfill
CN104261741A (en) Waste concrete geopolymer road base material
CN111170669A (en) Artificial recycled aggregate prepared from engineering waste soil and preparation method thereof
CN114573306A (en) High-strength rapid-setting concrete repairing material and preparation method and application thereof
CN112079594A (en) Geological polymer high-strength mortar for concrete structure repair and preparation method thereof
CN114230249B (en) Inorganic polymer mortar and preparation method thereof
CN113896475B (en) Method for preparing high-strength baking-free solid bricks by using rock wool furnace bottom slag
CN113845350A (en) Coal ash-based geopolymer modified coal gangue concrete building block and preparation method thereof
CN113277774A (en) Elastic curing ballast bed material and indoor test piece forming and manufacturing method thereof
CN109320157B (en) Coal mine goaf filling paste prepared from waste automobile tires by materials and preparation method thereof
CN105152626A (en) Technology for production of non-sintered ceramic through microwave maintenance of feldspath-quartz tailing
CN102924035A (en) Method for preparing geopolymer cementitious material by using diatomite
CN112299794A (en) Carbon-glass hybrid fiber modified rubber concrete and preparation method thereof
CN102850037A (en) Production process and formula of novel environment-friendly fly ash load-bearing brick
CN112745081A (en) Novel environment-friendly building material brick and preparation method thereof
CN101774221B (en) Method for producing light and novel reinforced concrete wall materials by blending slag micropowder

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