CN106146036A - Curing compound - Google Patents
Curing compound Download PDFInfo
- Publication number
- CN106146036A CN106146036A CN201610488072.4A CN201610488072A CN106146036A CN 106146036 A CN106146036 A CN 106146036A CN 201610488072 A CN201610488072 A CN 201610488072A CN 106146036 A CN106146036 A CN 106146036A
- Authority
- CN
- China
- Prior art keywords
- parts
- polyethylene glycol
- styrene
- solution
- butyl
- 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
Links
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
- C04B40/04—Preventing evaporation of the mixing water
-
- 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
- C04B40/02—Selection of the hardening environment
- C04B40/0277—Hardening promoted by using additional water, e.g. by spraying water on the green concrete element
- C04B40/029—Hardening promoted by using additional water, e.g. by spraying water on the green concrete element using an aqueous solution or dispersion
Abstract
The invention discloses a kind of curing compound, it includes the component of following mass fraction: styrene-acrylic emulsion 20～25 parts, acrylamide solution 7～10 parts, sodium silicate solution 7～9 parts, organic silicon solution 6～8 parts, methyl methacrylate 1～3 parts, monomethyl polyethylene glycol acrylate ester 1～3 parts, Polyethylene Glycol 3～5 parts, polyvinyl alcohol 1～3 parts, styrene 4～6 parts, acrylic acid methyl ester. 6～8 parts, butyl methacrylate 5～7 parts, butyl acrylate 3～5 parts, ethyl methacrylate 4～6 parts, Ammonium hyposulfite. 1～3 parts, ethylene propylene diene rubber 1～3 parts, butyl citrate 0.7 part, soda 1 part, Gypsum Fibrosum powder 0.5 part, periodate lignin 0.1 part, 0.1 part of surfactant, defoamer 0.2 part, levelling agent 0.3 part and benzyl alcohol 1 part.Sealing compound disclosed by the invention can effectively prevent inside concrete moisture loss, and environment friendly and pollution-free.
Description
Technical field
The present invention relates to a kind of curing compound.
Background technology
After cement concrete pours, it is necessary to have the temperature and humidity of necessity during initial set, enough to ensure
Moisture makes hydration reaction carry out completely, and traditional maintenance process litters bag, plastic sheeting and watering method of curing, and these methods are taken
Thing, laborious, it is impossible to effectively intercepting moisture evaporation, protective rate is low, and maintenance effect is the best.People usually select concrete to support at present
Protect agent to concrete curing, but current curing compound cannot effectively prevent the accumulation of salt in the surface soil phenomenon of pore.
Summary of the invention
It is an object of the invention to solve at least the above, and the advantage that at least will be described later is provided.
It is a still further object of the present invention to provide a kind of curing compound, it can effectively prevent inside concrete moisture
Scatter and disappear, and environment friendly and pollution-free.
In order to realize according to object of the present invention and further advantage, it is provided that a kind of curing compound, described mixed
Solidifying soil sealing compound includes the component of following mass fraction:
Styrene-acrylic emulsion 20～25 parts, acrylamide solution 7～10 parts, sodium silicate solution 7～9 parts, organic silicon solution 6～8
Part, methyl methacrylate 1～3 parts, monomethyl polyethylene glycol acrylate ester 1～3 parts, Polyethylene Glycol 3～5 parts, polyvinyl alcohol
(coalescents) 1～3 part, styrene 4～6 parts, acrylic acid methyl ester. 6～8 parts, butyl methacrylate 5～7 parts, acrylic acid fourth
Ester 3～5 parts, ethyl methacrylate 4～6 parts, Ammonium hyposulfite. 1～3 parts, ethylene propylene diene rubber 1～3 parts, butyl citrate
0.7 part, soda 1 part, Gypsum Fibrosum powder 0.5 part, periodate lignin 0.1 part, 0.1 part of surfactant, defoamer 0.2 part, stream
Flat agent 0.3 part and benzyl alcohol 1 part；
Wherein, the weight percent concentration of styrene-acrylic emulsion is 25%, and the weight percent concentration of acrylamide is 15%, silicon
The weight percent concentration of acid sodium solution is 25%；
The number-average molecular weight of Polyethylene Glycol is 500～1000, and the number-average molecular weight of monomethyl polyethylene glycol acrylate ester is
1200～1400.
Preferably, in described curing compound, described curing compound includes the component of following mass fraction:
Styrene-acrylic emulsion 20 parts, acrylamide solution 7 parts, sodium silicate solution 7 parts, organic silicon solution 6 parts, methyl methacrylate
Ester 1 part, monomethyl polyethylene glycol acrylate ester 1 part, Polyethylene Glycol 3 parts, polyvinyl alcohol 1 part, styrene 4 parts, acrylic acid methyl ester. 6
Part, butyl methacrylate 5 parts, butyl acrylate 3 parts, ethyl methacrylate 4 parts, Ammonium hyposulfite. 1 part, ethylene-propylene-diene monomer
1 part of glue, butyl citrate 0.7 part, soda 1 part, Gypsum Fibrosum powder 0.5 part, periodate lignin 0.1 part, surfactant 0.1
Part, defoamer 0.2 part, levelling agent 0.3 part and benzyl alcohol 1 part.
Preferably, in described curing compound, described curing compound includes the component of following mass fraction:
Styrene-acrylic emulsion 25 parts, acrylamide solution 10 parts, sodium silicate solution 9 parts, organic silicon solution 8 parts, methacrylic acid
Methyl ester 3 parts, monomethyl polyethylene glycol acrylate ester 3 parts, Polyethylene Glycol 5 parts, polyvinyl alcohol 3 parts, styrene 6 parts, acrylic acid first
Ester 8 parts, butyl methacrylate 7 parts, butyl acrylate 5 parts, ethyl methacrylate 6 parts, Ammonium hyposulfite. 3 parts, ternary second
Third rubber 3 parts, butyl citrate 0.7 part, soda 1 part, Gypsum Fibrosum powder 0.5 part, periodate lignin 0.1 part, surfactant
0.1 part, defoamer 0.2 part, levelling agent 0.3 part and benzyl alcohol 1 part.
Preferably, in described curing compound, described curing compound includes the component of following mass fraction:
Styrene-acrylic emulsion 23 parts, acrylamide solution 9 parts, sodium silicate solution 8 parts, organic silicon solution 7 parts, methyl methacrylate
Ester 2 parts, monomethyl polyethylene glycol acrylate ester 2 parts, Polyethylene Glycol 4 parts, polyvinyl alcohol 2 parts, styrene 5 parts, acrylic acid methyl ester. 7
Part, butyl methacrylate 6 parts, butyl acrylate 4 parts, ethyl methacrylate 5 parts, Ammonium hyposulfite. 2 parts, ethylene-propylene-diene monomer
2 parts of glue, butyl citrate 0.7 part, soda 1 part, Gypsum Fibrosum powder 0.5 part, periodate lignin 0.1 part, surfactant 0.1
Part, defoamer 0.2 part, levelling agent 0.3 part and benzyl alcohol 1 part
Preferably, in described curing compound, surfactant includes the component of following mass fraction: alkylbenzene
Sodium sulfonate 40%, liver sodium cholate 30% and 30% fatty glyceride.
The present invention at least includes following beneficial effect: the first, sealing compound disclosed by the invention is formed even at concrete surface layer
Continuous colourless fluid-tight efficient curing membrane, prevents the evaporation of moisture, can penetrate again to concrete pore, with cement water
Change product reaction and generate insoluble matter blocking pore, plug the passage that the water of pore outwards evaporates, capillary can be reduced simultaneously
The surface tension of water in hole, reduces pore water additonal pressure, reduces the dry shrinkage of concrete, plays and well reduces, protects
Water curing effect, promotes the abundant aquation of cement, improves the intensity of concrete, reduces the desciccation crack of concrete.The second, the present invention
In non-volatile material, and nontoxic, tasteless, environmentally safe, easy to use, it is adaptable to the concrete table of various environment and condition
Layer, is particularly suited for the concrete of the new cast in dry area；3rd, the organosilan contained, it can infiltrate into rapidly
Inside concrete, and react generation silicon dioxide with the water and air in concrete, block capillary porosity duct, formed waterproof
Layer, effectively prevents inside concrete water loss.
Part is embodied by the further advantage of the present invention, target and feature by description below, and part also will be by this
Invention research and practice and be understood by the person skilled in the art.
Detailed description of the invention
Below in conjunction with embodiment, the present invention is described in further detail, to make those skilled in the art with reference to description
Word can be implemented according to this.
Should be appreciated that used herein such as " have ", " comprising " and " including " term do not allot one or many
Other element individual or the existence of a combination thereof or interpolation.
Embodiment 1
A kind of curing compound, this curing compound includes:
Styrene-acrylic emulsion 22Kg, acrylamide solution 9Kg, sodium silicate solution 7Kg, organic silicon solution 8Kg, methyl methacrylate
Ester 3Kg, monomethyl polyethylene glycol acrylate ester 2Kg, Polyethylene Glycol 4Kg, polyvinyl alcohol 3Kg, styrene 5Kg, acrylic acid methyl ester.
6Kg, butyl methacrylate 6Kg, butyl acrylate 3Kg, ethyl methacrylate 6Kg, Ammonium hyposulfite. 3Kg, EPDM
Rubber 3Kg, butyl citrate 0.7Kg, soda 1Kg, Gypsum Fibrosum powder 0.5Kg, periodate lignin 0.1Kg, surfactant
0.1Kg, defoamer 0.2Kg, levelling agent 0.3Kg and benzyl alcohol 1Kg；
Wherein, the weight percent concentration of styrene-acrylic emulsion is 25%, and the weight percent concentration of acrylamide is 15%, silicon
The weight percent concentration of acid sodium solution is 25%；
The number-average molecular weight of Polyethylene Glycol is 500～1000, and the number-average molecular weight of monomethyl polyethylene glycol acrylate ester is
1200～1400；
Surfactant includes the component of following mass fraction: sodium alkyl benzene sulfonate 40%, liver sodium cholate 30% and 30%
Fatty glyceride.
According to the test method of JC901-2002, the effective water retention of curing compound provided in the present embodiment is carried out
Checking；Concrete abrasion amount test is carried out according to JTJ053；Concrete test drying time is carried out according to JC/T421；According to
JC901-2002 carries out concrete crushing strength than test；Concrete osmotic pressure ratio test is carried out according to JC474-1999；On
State test structure and be shown in Table one.
The every result of the test of table one
Intrusion dissolubility test after film forming:
Sealing compound is once applied on the plate of 150mm × 200mm by test consumption, after being completely dried, is immersed in the water, water
Temperature is 20 ± 3 DEG C, and soaking time is 1h, observes whether film dissolves, and result is insoluble.
Film forming heat-resistance test:
Sealing compound is applied on glass plate by test consumption, after being completely dried, is placed in the drying baker of 65 ± 2 DEG C, permanent
See whether after temperature 10min to occur to melt, metachromatism, result for not melting, invariant color.
Embodiment 2,
A kind of curing compound, this curing compound includes:
Styrene-acrylic emulsion 20Kg, acrylamide solution 7Kg, sodium silicate solution 7Kg, organic silicon solution 6Kg, methyl methacrylate
Ester 1Kg, monomethyl polyethylene glycol acrylate ester 1Kg, Polyethylene Glycol 3Kg, polyvinyl alcohol 1Kg, styrene 4Kg, acrylic acid methyl ester.
6Kg, butyl methacrylate 5Kg, butyl acrylate 3Kg, ethyl methacrylate 4Kg, Ammonium hyposulfite. 1Kg, EPDM
Rubber 1Kg, butyl citrate 0.7Kg, soda 1Kg, Gypsum Fibrosum powder 0.5Kg, periodate lignin 0.1Kg, surfactant
0.1Kg, defoamer 0.2Kg, levelling agent 0.3Kg and benzyl alcohol 1Kg；
Wherein, the weight percent concentration of styrene-acrylic emulsion is 25%, and the weight percent concentration of acrylamide is 15%, silicon
The weight percent concentration of acid sodium solution is 25%；
The number-average molecular weight of Polyethylene Glycol is 500～1000, and the number-average molecular weight of monomethyl polyethylene glycol acrylate ester is
1200～1400；
Surfactant includes the component of following mass fraction: sodium alkyl benzene sulfonate 40%, liver sodium cholate 30% and 30%
Fatty glyceride.
According to the test method of JC901-2002, the effective water retention of curing compound provided in the present embodiment is carried out
Checking；Concrete abrasion amount test is carried out according to JTJ053；Concrete test drying time is carried out according to JC/T421；According to
JC901-2002 carries out concrete crushing strength than test；Concrete osmotic pressure ratio test is carried out according to JC474-1999；On
State test structure and be shown in Table two.
The every result of the test of table two
Intrusion dissolubility test after film forming:
Sealing compound is once applied on the plate of 150mm × 200mm by test consumption, after being completely dried, is immersed in the water, water
Temperature is 20 ± 3 DEG C, and soaking time is 1h, observes whether film dissolves, and result is insoluble.
Film forming heat-resistance test:
Sealing compound is applied on glass plate by test consumption, after being completely dried, is placed in the drying baker of 65 ± 2 DEG C, permanent
See whether after temperature 10min to occur to melt, metachromatism, result for not melting, invariant color.
Embodiment 3,
A kind of curing compound, this curing compound includes:
Styrene-acrylic emulsion 25Kg, acrylamide solution 10Kg, sodium silicate solution 9Kg, organic silicon solution 8Kg, methacrylic acid
Methyl ester 3Kg, monomethyl polyethylene glycol acrylate ester 3Kg, Polyethylene Glycol 5Kg, polyvinyl alcohol 3Kg, styrene 6Kg, acrylic acid first
Ester 8Kg, butyl methacrylate 7Kg, butyl acrylate 5Kg, ethyl methacrylate 6Kg, Ammonium hyposulfite. 3Kg, ternary second
Third rubber 3Kg, butyl citrate 0.7Kg, soda 1Kg, Gypsum Fibrosum powder 0.5Kg, periodate lignin, surfactant 0.1Kg,
Defoamer 0.2Kg, levelling agent 0.3Kg and benzyl alcohol 1Kg；
Wherein, the weight percent concentration of styrene-acrylic emulsion is 25%, and the weight percent concentration of acrylamide is 15%, silicon
The weight percent concentration of acid sodium solution is 25%；
The number-average molecular weight of Polyethylene Glycol is 500～1000, and the number-average molecular weight of monomethyl polyethylene glycol acrylate ester is
1200～1400；
Surfactant includes the component of following mass fraction: sodium alkyl benzene sulfonate 40%, liver sodium cholate 30% and 30%
Fatty glyceride.
According to the test method of JC901-2002, the effective water retention of curing compound provided in the present embodiment is carried out
Checking；Concrete abrasion amount test is carried out according to JTJ053；Concrete test drying time is carried out according to JC/T421；According to
JC901-2002 carries out concrete crushing strength than test；Concrete osmotic pressure ratio test is carried out according to JC474-1999；On
State test structure and be shown in Table three.
The every result of the test of table three
Intrusion dissolubility test after film forming:
Sealing compound is once applied on the plate of 150mm × 200mm by test consumption, after being completely dried, is immersed in the water, water
Temperature is 20 ± 3 DEG C, and soaking time is 1h, observes whether film dissolves, and result is insoluble.
Film forming heat-resistance test:
Sealing compound is applied on glass plate by test consumption, after being completely dried, is placed in the drying baker of 65 ± 2 DEG C, permanent
See whether after temperature 10min to occur to melt, metachromatism, result for not melting, invariant color.
Embodiment 4,
A kind of curing compound, this curing compound includes:
Styrene-acrylic emulsion 23Kg, acrylamide solution 9Kg, sodium silicate solution 8Kg, organic silicon solution 7Kg, methyl methacrylate
Ester 2Kg, monomethyl polyethylene glycol acrylate ester 2Kg, Polyethylene Glycol 4Kg, polyvinyl alcohol 2Kg, styrene 5Kg, acrylic acid methyl ester.
7Kg, butyl methacrylate 6Kg, butyl acrylate 4Kg, ethyl methacrylate 5Kg, Ammonium hyposulfite. 2Kg, EPDM
Rubber 2Kg, butyl citrate 0.7Kg, soda 1Kg, Gypsum Fibrosum powder 0.5Kg, periodate lignin 0.1Kg, surfactant
0.1Kg, defoamer 0.2Kg, levelling agent 0.3Kg and benzyl alcohol 1Kg；
Wherein, the weight percent concentration of styrene-acrylic emulsion is 25%, and the weight percent concentration of acrylamide is 15%, silicon
The weight percent concentration of acid sodium solution is 25%；
The number-average molecular weight of Polyethylene Glycol is 500～1000, and the number-average molecular weight of monomethyl polyethylene glycol acrylate ester is
1200～1400；
Surfactant includes the component of following mass fraction: sodium alkyl benzene sulfonate 40%, liver sodium cholate 30% and 30%
Fatty glyceride.
According to the test method of JC901-2002, the effective water retention of curing compound provided in the present embodiment is carried out
Checking；Concrete abrasion amount test is carried out according to JTJ053；Concrete test drying time is carried out according to JC/T421；According to
JC901-2002 carries out concrete crushing strength than test；Concrete osmotic pressure ratio test is carried out according to JC474-1999；On
State test structure and be shown in Table three.
The every result of the test of table three
Intrusion dissolubility test after film forming:
Sealing compound is once applied on the plate of 150mm × 200mm by test consumption, after being completely dried, is immersed in the water, water
Temperature is 20 ± 3 DEG C, and soaking time is 1h, observes whether film dissolves, and result is insoluble.
Film forming heat-resistance test:
Sealing compound is applied on glass plate by test consumption, after being completely dried, is placed in the drying baker of 65 ± 2 DEG C, permanent
See whether after temperature 10min to occur to melt, metachromatism, result for not melting, invariant color.
Although embodiment of the present invention are disclosed as above, but it is not restricted in description and embodiment listed
Using, it can be applied to various applicable the field of the invention completely, for those skilled in the art, and can be easily
Realizing other amendment, therefore under the general concept limited without departing substantially from claim and equivalency range, the present invention does not limit
In specific details.
Claims (5)
1. a curing compound, it is characterised in that described curing compound includes the component of following mass fraction:
Styrene-acrylic emulsion 20～25 parts, acrylamide solution 7～10 parts, sodium silicate solution 7～9 parts, organic silicon solution 6～8 parts, first
Base acrylic acid methyl ester. 1～3 parts, monomethyl polyethylene glycol acrylate ester 1～3 parts, Polyethylene Glycol 3～5 parts, polyvinyl alcohol 1～3
Part, styrene 4～6 parts, acrylic acid methyl ester. 6～8 parts, butyl methacrylate 5～7 parts, butyl acrylate 3～5 parts, methyl-prop
Olefin(e) acid ethyl ester 4～6 parts, Ammonium hyposulfite. 1～3 parts, ethylene propylene diene rubber 1～3 parts, butyl citrate 0.7 part, soda 1 part, stone
0.5 part of cream powder, periodate lignin 0.1 part, 0.1 part of surfactant, defoamer 0.2 part, levelling agent 0.3 part and benzyl alcohol
1 part；
Wherein, the weight percent concentration of styrene-acrylic emulsion is 25%, and the weight percent concentration of acrylamide is 15%, sodium silicate
The weight percent concentration of solution is 25%；
The number-average molecular weight of Polyethylene Glycol is 500～1000, and the number-average molecular weight of monomethyl polyethylene glycol acrylate ester is 1200
～1400.
2. curing compound as claimed in claim 1, it is characterised in that described curing compound includes following mass parts
The component of number:
Styrene-acrylic emulsion 20 parts, acrylamide solution 7 parts, sodium silicate solution 7 parts, organic silicon solution 6 parts, methyl methacrylate 1
Part, monomethyl polyethylene glycol acrylate ester 1 part, Polyethylene Glycol 3 parts, polyvinyl alcohol 1 part, styrene 4 parts, acrylic acid methyl ester. 6 parts,
Butyl methacrylate 5 parts, butyl acrylate 3 parts, ethyl methacrylate 4 parts, Ammonium hyposulfite. 1 part, ethylene propylene diene rubber 1
Part, butyl citrate 0.7 part, soda 1 part, Gypsum Fibrosum powder 0.5 part, periodate lignin 0.1 part, 0.1 part of surfactant, disappear
Infusion 0.2 part, levelling agent 0.3 part and benzyl alcohol 1 part.
3. curing compound as claimed in claim 1, it is characterised in that described curing compound includes following mass parts
The component of number:
Styrene-acrylic emulsion 25 parts, acrylamide solution 10 parts, sodium silicate solution 9 parts, organic silicon solution 8 parts, methyl methacrylate 3
Part, monomethyl polyethylene glycol acrylate ester 3 parts, Polyethylene Glycol 5 parts, polyvinyl alcohol 3 parts, styrene 6 parts, acrylic acid methyl ester. 8 parts,
Butyl methacrylate 7 parts, butyl acrylate 5 parts, ethyl methacrylate 6 parts, Ammonium hyposulfite. 3 parts, ethylene propylene diene rubber 3
Part, butyl citrate 0.7 part, soda 1 part, Gypsum Fibrosum powder 0.5 part, periodate lignin 0.1 part, 0.1 part of surfactant, disappear
Infusion 0.2 part, levelling agent 0.3 part and benzyl alcohol 1 part.
4. curing compound as claimed in claim 1, it is characterised in that described curing compound includes following mass parts
The component of number:
Styrene-acrylic emulsion 23 parts, acrylamide solution 9 parts, sodium silicate solution 8 parts, organic silicon solution 7 parts, methyl methacrylate 2
Part, monomethyl polyethylene glycol acrylate ester 2 parts, Polyethylene Glycol 4 parts, polyvinyl alcohol 2 parts, styrene 5 parts, acrylic acid methyl ester. 7 parts,
Butyl methacrylate 6 parts, butyl acrylate 4 parts, ethyl methacrylate 5 parts, Ammonium hyposulfite. 2 parts, ethylene propylene diene rubber 2
Part, butyl citrate 0.7 part, soda 1 part, Gypsum Fibrosum powder 0.5 part, periodate lignin 0.1 part, 0.1 part of surfactant, disappear
Infusion 0.2 part, levelling agent 0.3 part and benzyl alcohol 1 part.
5. curing compound as claimed in any one of claims 1 to 5, wherein, it is characterised in that surfactant includes following
The component of mass fraction: sodium alkyl benzene sulfonate 40%, liver sodium cholate 30% and 30% fatty glyceride.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610488072.4A CN106146036A (en) | 2016-06-28 | 2016-06-28 | Curing compound |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610488072.4A CN106146036A (en) | 2016-06-28 | 2016-06-28 | Curing compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN106146036A true CN106146036A (en) | 2016-11-23 |
Family
ID=57349543
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201610488072.4A Pending CN106146036A (en) | 2016-06-28 | 2016-06-28 | Curing compound |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106146036A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106977230A (en) * | 2017-05-14 | 2017-07-25 | 石磊 | A kind of preparation method of water conservation self-repair type curing compound |
| CN107010994A (en) * | 2017-04-14 | 2017-08-04 | 农文书 | Ultra-high performance concrete conserves the preparation method of powder |
| CN107010995A (en) * | 2017-04-14 | 2017-08-04 | 农文书 | The preparation method of curing compound with nano material |
| CN109704670A (en) * | 2019-02-27 | 2019-05-03 | 南昌航空大学 | A kind of graphene modified concrete |
| CN109987966A (en) * | 2019-04-24 | 2019-07-09 | 中国路桥工程有限责任公司 | Curing compound |
| CN114805824A (en) * | 2022-05-06 | 2022-07-29 | 苏光伟 | Multifunctional concrete additive and preparation method and application thereof |
| CN115259897A (en) * | 2022-07-07 | 2022-11-01 | 山西佳维新材料股份有限公司 | Organic-inorganic composite concrete curing agent, preparation method and concrete curing method |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101219867A (en) * | 2008-01-28 | 2008-07-16 | 潍坊市大元实业有限公司 | Concrete maintaining agent |
| CN101531482A (en) * | 2009-04-22 | 2009-09-16 | 江苏鼎达建材有限公司 | Shrinkage reducing and curing agent for concrete |
| CN102603401A (en) * | 2012-03-16 | 2012-07-25 | 陕西汉唐环保农业有限公司 | High-potassium liquid organic fertilizer taking wood vinegar as matrix and production method thereof |
| CN103073220A (en) * | 2013-01-16 | 2013-05-01 | 江苏博特新材料有限公司 | Emulsion type concrete curing agent |
| CN104987127A (en) * | 2015-06-29 | 2015-10-21 | 青岛祥嘉知识产权服务有限公司 | Long-lasting concrete curing compound |
-
2016
- 2016-06-28 CN CN201610488072.4A patent/CN106146036A/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101219867A (en) * | 2008-01-28 | 2008-07-16 | 潍坊市大元实业有限公司 | Concrete maintaining agent |
| CN101531482A (en) * | 2009-04-22 | 2009-09-16 | 江苏鼎达建材有限公司 | Shrinkage reducing and curing agent for concrete |
| CN102603401A (en) * | 2012-03-16 | 2012-07-25 | 陕西汉唐环保农业有限公司 | High-potassium liquid organic fertilizer taking wood vinegar as matrix and production method thereof |
| CN103073220A (en) * | 2013-01-16 | 2013-05-01 | 江苏博特新材料有限公司 | Emulsion type concrete curing agent |
| CN104987127A (en) * | 2015-06-29 | 2015-10-21 | 青岛祥嘉知识产权服务有限公司 | Long-lasting concrete curing compound |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107010994A (en) * | 2017-04-14 | 2017-08-04 | 农文书 | Ultra-high performance concrete conserves the preparation method of powder |
| CN107010995A (en) * | 2017-04-14 | 2017-08-04 | 农文书 | The preparation method of curing compound with nano material |
| CN106977230A (en) * | 2017-05-14 | 2017-07-25 | 石磊 | A kind of preparation method of water conservation self-repair type curing compound |
| CN109704670A (en) * | 2019-02-27 | 2019-05-03 | 南昌航空大学 | A kind of graphene modified concrete |
| CN109704670B (en) * | 2019-02-27 | 2021-09-14 | 南昌航空大学 | Graphene modified concrete |
| CN109987966A (en) * | 2019-04-24 | 2019-07-09 | 中国路桥工程有限责任公司 | Curing compound |
| CN109987966B (en) * | 2019-04-24 | 2021-11-09 | 中国路桥工程有限责任公司 | Concrete curing agent |
| CN114805824A (en) * | 2022-05-06 | 2022-07-29 | 苏光伟 | Multifunctional concrete additive and preparation method and application thereof |
| CN115259897A (en) * | 2022-07-07 | 2022-11-01 | 山西佳维新材料股份有限公司 | Organic-inorganic composite concrete curing agent, preparation method and concrete curing method |
| CN115259897B (en) * | 2022-07-07 | 2023-06-20 | 山西佳维新材料股份有限公司 | Organic-inorganic composite concrete curing agent, preparation method and concrete curing method |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN106146036A (en) | Curing compound | |
| CN101219867B (en) | Concrete maintaining agent | |
| CN104230376B (en) | Organic silicon emulsion-Ludox permeable crystalline waterproofing material and preparation method thereof | |
| US20070208109A1 (en) | Additive building material mixtures containing swellable polymeric formations | |
| AU2016378276B2 (en) | Contact layer with mineral binder component | |
| CN102515616B (en) | Composite slump-loss-resistant polycarboxylic acid water reducing agent and preparation method thereof | |
| WO2009047126A4 (en) | Laundry detergent with pretreatment additive and its use | |
| BR0212350B1 (en) | process for manufacturing cementitious particles. | |
| CN106366239A (en) | Macromolecular polymer water-proofing agent and preparation method and usage method thereof | |
| CN105254802A (en) | Waterproof emulsion and preparation method thereof | |
| CN104710849B (en) | A kind of spray film water-proofing material and its preparation and application | |
| CN106010569A (en) | Organic-inorganic compound chemical sand fixing agent and preparation method thereof | |
| CN102757196A (en) | Waterproof cement additive and cement containing same | |
| JP2004323333A (en) | Concrete modifier | |
| CN103232745A (en) | Transparent elastic putty and preparation method thereof | |
| CN107010994A (en) | Ultra-high performance concrete conserves the preparation method of powder | |
| CN106749943A (en) | A kind of wear-resisting lucite and preparation method thereof | |
| US20190276372A1 (en) | Concrete protective agent and preparation method thereof, and concrete protective film and preparation method thereof | |
| RU2016142397A (en) | METHOD OF ROTARY PRINT FOR APPLICATION OF MAGNETIC COMPOSITIONS | |
| CN105294161B (en) | A kind of unsaturated siloxane base phosphate lotion curing compound and preparation method thereof | |
| CN102877306A (en) | Method for manufacturing waterstop strap subjected to small influence of ions | |
| WO2018056705A1 (en) | Envelope-type detergent having enhanced resistance to water | |
| CN106752426A (en) | The super infiltration interfacial agents preparation method of aqueous, environmental protective | |
| KR101793780B1 (en) | Permeable complex waterproof material | |
| CN107903084A (en) | The clear-water concrete protective agent and its application process of a kind of high-weatherability |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20161123 |
|
| RJ01 | Rejection of invention patent application after publication |