CN108424082A - A kind of preparation method of pleat-free cement-base waterproof coating - Google Patents

A kind of preparation method of pleat-free cement-base waterproof coating Download PDF

Info

Publication number
CN108424082A
CN108424082A CN201810355075.XA CN201810355075A CN108424082A CN 108424082 A CN108424082 A CN 108424082A CN 201810355075 A CN201810355075 A CN 201810355075A CN 108424082 A CN108424082 A CN 108424082A
Authority
CN
China
Prior art keywords
parts
cement
pleat
waterproof coating
water
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
CN201810355075.XA
Other languages
Chinese (zh)
Inventor
俞小峰
朱冬梅
吴庆梅
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CN201810355075.XA priority Critical patent/CN108424082A/en
Publication of CN108424082A publication Critical patent/CN108424082A/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
    • 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
    • C04B28/02Compositions 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 hydraulic cements other than calcium sulfates
    • C04B28/04Portland cements
    • 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
    • C04B20/00Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
    • C04B20/02Treatment
    • C04B20/023Chemical treatment
    • 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
    • C04B20/00Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
    • C04B20/02Treatment
    • C04B20/026Comminuting, e.g. by grinding or breaking; Defibrillating fibres other than asbestos
    • 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
    • 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
    • C04B28/02Compositions 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 hydraulic cements other than calcium sulfates
    • C04B28/06Aluminous cements
    • 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
    • C04B2111/00482Coating or impregnation materials
    • 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
    • C04B2111/20Resistance against chemical, physical or biological attack
    • C04B2111/27Water resistance, i.e. waterproof or water-repellent materials
    • 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
    • C04B2201/00Mortars, concrete or artificial stone characterised by specific physical values
    • C04B2201/50Mortars, concrete or artificial stone characterised by specific physical values for the mechanical strength

Abstract

The invention discloses a kind of preparation methods of pleat-free cement-base waterproof coating, belong to building material technical field.Diatomite is mixed ultrasound with butyl titanate by the present invention, and filtering obtains pretreatment diatomite, will pre-process diatomite, graphene oxide, paraffin, sodium bicarbonate ball milling mixing, sieving is to get modification infusorial earth;By aggregate, dopamine solution, biogas slurry, glucose solution mixed fermentation is filtered, dry, obtains pretreatment aggregate;By cement, aggregate is pre-processed, modification infusorial earth, clay, forsterite powder, organic siliconresin, water-reducing agent, silane coupling agent, surfactant, alkalescent phenol resin, curing agent, water is stirred to get pleat-free cement-base waterproof coating.

Description

A kind of preparation method of pleat-free cement-base waterproof coating
Technical field
The invention discloses a kind of preparation methods of pleat-free cement-base waterproof coating, belong to building material technical field.
Background technology
In recent years, with the raising and accumulation of water-based waterproofing paint properties of product, application experience, product annual growth is always Keep ascendant trend.Although solvent borne polyurethane water-repellent paint has excellent comprehensive performance, reach level-one waterproof effect;But because In product form more and more limitations have been received containing harmful substances, application ranges such as anthracene, naphthalene, phenol, organic solvents.And Water base building water-proof paint is using water as carrier, safety and environmental protection, adapts to the waterproofing work of a variety of profiled-cross-section buildings base.Work as peace Entirely, when environmental protection becomes human survival with development primary need, the development of modern industry must be as basic principle.Water base waterproof applies Expect a large amount of organic solvent in water consumption substitution solvent-type waterproofing paint, meets green low-carbon environment-friendly requirement, with product technology Horizontal continuous improvement, will provide more solid guarantee for construction waterproofing engineering.Water base building water-proof paint water-proof mechanism has painting Two kinds of film waterproof and hydrophobic waterproof.After coating application, with the volatilization of dampening, latex particle mutually squeezes, condenses into fine and close painting Film.It is this to stop that the method that hydrone infiltration or water penetrate is known as coating waterproofing using film.Although made of fusion condensation Macromolecular coating is intermolecular to have certain gap, but hydrone is typically existed with state of associating, by hydrogen bond action after association Hydrone be difficult to through film.Aqueous-based polymers molecular structure carries hydrophilic radical, and the polymer of immersion applies for a long time Film can be slowly swollen, and influence waterproof effect;So individually water base film can not block water completely.In order to improve polymer Hydrophobicity usually introduces hydrophobic grouping the molecular structure of polymer, enhances the hydrophobicity of polymer itself, makes hydrone and applies Film is incompatible, prevents hydrone from permeating.This method penetrated using hydrophobic grouping blocking water is known as hydrophobic waterproof.Building because The temperature difference, settlement of foundation, structure design, construction quality influence and generate cracking phenomena when have been reported that, the leak of new and old building object, Seepage problem has been one of main Quality of building trade.In face of the cracking, water-based coating self-defect, consumer of base material The increasingly raising of decoration demand, the following water-repellent paint are wideling popularize development promotion coating water permeability resistance, tensile strength, anti-folding by force It spends, the change functionality direction of tensile splitting strength is developed
Therefore, how to improve the low disadvantage of traditional water permeability resistance, tensile strength, flexural strength, tensile splitting strength, to obtain more The raising of high combination property is that it is promoted and applies, meets industrial production demand urgent problem to be solved.
Invention content
The present invention solves the technical problem of:It is anti-for traditional water permeability resistance, tensile strength, flexural strength, splitting The low disadvantage of tensile strength, provides that the invention discloses a kind of preparation methods of pleat-free cement-base waterproof coating.
In order to solve the above-mentioned technical problem, the technical solution adopted in the present invention is:
A kind of preparation method of pleat-free cement-base waterproof coating, it is characterised in that specific preparation process is as follows:
(1)By diatomite and butyl titanate in mass ratio 1:30~1:50 mixing ultrasounds, filtering obtain pretreatment diatomite, press Parts by weight meter pre-processes diatomite, 10~20 parts of graphene oxides, 60~80 parts of paraffin, 10~20 parts of carbon by 10~20 parts Sour hydrogen sodium ball milling mixing is sieved to get modification infusorial earth;
(2)It counts in parts by weight, by 20~30 parts of aggregates, 10~20 parts of dopamine solutions, 3~5 parts of biogas slurries, 30~40 portions of grapes Sugar juice ferments, and filters, dry, obtains pretreatment aggregate;
(3)It counts in parts by weight, by 50~60 parts of cement, 50~60 parts of pretreatment aggregates, 10~20 parts of modification infusorial earths, 10~ 20 parts of clays, 10~20 parts of forsterite powder, 10~20 parts of organic siliconresins, 5~8 parts of water-reducing agents, 5~8 parts of silane coupling agents, 5~8 parts of surfactants, 10~20 parts of alkalescent phenol resins, 3~5 parts of curing agent, 60~80 parts of water are stirred to get anti- Fold-type cement-base waterproof coating.
Step(2)The aggregate is river sand, mountain sand, sea sand, any one in aggregate chips or waste residue sand.
Step(3)The cement is portland cement, any one in aluminate cement or sulfate cement.
Step(3)The organic siliconresin is methyl trichlorosilane, in dimethyldichlorosilane or phenyl trichlorosilane Any one.
Step(3)The water-reducing agent is sodium lignin sulfonate, and TH-928 poly carboxylic acid series water reducers or YZ-1 naphthalene series high-efficiencies subtract Any one in aqua.
Step(3)The silane coupling agent is silane resin acceptor kh-550, silane coupling agent KH-560 or silane coupling agent Any one in KH-570.
Step(3)The surfactant is any one of polyethylene glycol, alkyl glycosides or neopelex.
Step(3)The preparation process of the alkalescent phenol resin is:It counts in parts by weight, 30~40 parts of glyoxals are molten Liquid, 10~20 parts of potassium hydroxide solutions, 30~40 parts of hydroquinone constant temperature are stirred to react, and glyoxal solution volume is added in cooling 0.2~0.3 times of ethylene urea is stirred to react, and the silane coupling agent KH- of 0.1~0.2 times of glyoxal solution volume is added in cooling 570 are stirred to react, and cool down to get alkalescent phenol resin.
Step(3)The curing agent is diethylenetriamine, any one in triethylene tetramine or dipropylenetriamine.
The beneficial effects of the invention are as follows:
(1)The present invention is paraffin melting in use by adding modification infusorial earth so that internal pretreatment diatomite and Graphene oxide exposes, and first, the butyl titanate pre-processed in diatomite is reacted with water, generates nano-titanium dioxide, is generated Nano-titanium dioxide be attached to pore surface, form nano-emulsion lug structure makes to increase the contact angle of water and pore surface The water resistance for the system of obtaining further is promoted, and secondly, graphene oxide has good hydrophilicity, can mix in the early stage It is dispersed in system in the process, the progress of subsequent hydrated cementitious, system pH gradually rises, and under basic conditions, aoxidizes stone Black alkene is reduced into graphene, since graphene surface does not have hydrophilic radical, graphene to be filled in system, further lifting body The water resistance of system;
(2)The present invention is by adding clay, due to the fine grain ion adsorption of clay, keeps formation aquation around particle thin Film, and capillary is formed between clay particle, when coating particles stress slides, moisture film hinders particle at nervous film It is detached from, so that the mechanical property of system is further promoted.
Specific implementation mode
It counts in parts by weight, the glyoxal solution for being 30~40% by 30~40 parts of mass fractions, 10~20 parts of mass fractions For 20~30% potassium hydroxide solution, 30~40 parts of hydroquinones are placed in four-hole boiling flask, and four-hole boiling flask is placed in digital display and is surveyed It is 76~78 DEG C in temperature in fast constant temperature blender with magnetic force, under the conditions of rotating speed is 300~500r/min, constant temperature is stirred to react 3~ After 4h, temperature in four-hole boiling flask is down to 60~62 DEG C, then 0.2~0.3 times of glyoxal solution volume is added into four-hole boiling flask Ethylene urea, in temperature be 60~62 DEG C, rotating speed be 300~500r/min under the conditions of, after constant temperature is stirred to react 40~60min, Temperature in four-hole boiling flask is down to 50~52 DEG C, the silicon of 0.1~0.2 times of glyoxal solution volume is then added into four-hole boiling flask Alkane coupling agent kh-570 is 50~52 DEG C in temperature, under the conditions of rotating speed is 300~500r/min, constant temperature is stirred to react 40~ Temperature in four-hole boiling flask is down to 40~42 DEG C by 50min, is 40~42 DEG C in temperature, rotating speed is 300~500r/min conditions Under, continue constant temperature and is stirred to react 20~30min to get alkalescent phenol resin;By diatomite and butyl titanate in mass ratio 1: 30~1:50 are placed in No. 1 beaker, and No. 1 beaker is placed in ultrasonic disperse instrument, in supersonic frequency be 55~75kHz conditions Under, 40~60min of ultrasonic disperse is mixed, dispersion liquid is obtained, then dispersion liquid is filtered, obtains pretreatment diatomite, count in parts by weight, Diatomite are pre-processed by 10~20 parts, 10~20 parts of graphene oxides, 60~80 parts of paraffin, 10~20 parts of sodium bicarbonates are placed in ball Ball milling mixing in grinding machine crosses the sieve of 80~100 mesh to get modification infusorial earth;It counts in parts by weight, by 20~30 parts of aggregates, 10 The dopamine solution that~20 parts of mass concentrations are 2.5mg/mL, 3~5 parts of biogas slurries, 30~40 parts of mass fractions are 0.3~0.5% Glucose solution is placed in fermentation cauldron, in temperature be 28~32 DEG C, rotating speed be 400~600r/min under the conditions of, mixed fermentation 3~ 5 days, zymotic fluid is obtained, then by filtering fermentation liquor, obtains filter cake, filter cake is then placed in drying in vacuum freezing drying oven, is obtained pre- Handle aggregate;It counts in parts by weight, by 50~60 parts of cement, 50~60 parts of pretreatment aggregates, 10~20 parts of modification infusorial earths, 10 ~20 parts of clays, 10~20 parts of forsterite powder, 10~20 parts of organic siliconresins, 5~8 parts of water-reducing agents, 5~8 parts silane coupled Agent, 5~8 parts of surfactants, 10~20 parts of alkalescent phenol resins, 3~5 parts of curing agent, 60~80 parts of water are placed in batch mixer, Under the conditions of rotating speed is 300~500r/min, 40~60min is stirred to get pleat-free cement-base waterproof coating.The bone Expect to be river sand, mountain sand, sea sand, any one in aggregate chips or waste residue sand.The cement be portland cement, aluminate cement or Any one in sulfate cement.The organic siliconresin is methyl trichlorosilane, dimethyldichlorosilane or phenyl trichlorine Any one in silane.The water-reducing agent is sodium lignin sulfonate, TH-928 poly carboxylic acid series water reducers or YZ-1 naphthalene series high-efficiencies Any one in water-reducing agent.The silane coupling agent is silane resin acceptor kh-550, and silane coupling agent KH-560 or silane are even Join any one in agent KH-570.The surfactant is polyethylene glycol, alkyl glycosides or neopelex Any one.The curing agent is diethylenetriamine, any one in triethylene tetramine or dipropylenetriamine.
Example 1
It counts in parts by weight, the glyoxal solution for being 40% by 40 parts of mass fractions, the potassium hydroxide that 20 parts of mass fractions are 30% Solution, 40 parts of hydroquinones are placed in four-hole boiling flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, Yu Wen Degree is 78 DEG C, and under the conditions of rotating speed is 500r/min, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, then to The ethylene urea of 0.3 times of glyoxal solution volume is added in four-hole boiling flask, in temperature be 62 DEG C, under the conditions of rotating speed is 500r/min, After constant temperature is stirred to react 60min, temperature in four-hole boiling flask is down to 52 DEG C, glyoxal solution body is then added into four-hole boiling flask The Silane coupling reagent KH-570 of 0.2 times of product is 52 DEG C in temperature, and under the conditions of rotating speed is 500r/min, constant temperature is stirred to react Temperature in four-hole boiling flask is down to 42 DEG C by 50min, is 42 DEG C in temperature, under the conditions of rotating speed is 500r/min, is continued constant temperature stirring 30min is reacted to get alkalescent phenol resin;By diatomite and butyl titanate in mass ratio 1:50 are placed in No. 1 beaker, and will No. 1 beaker is placed in ultrasonic disperse instrument, under the conditions of supersonic frequency is 75kHz, is mixed ultrasonic disperse 60min, is obtained dispersion liquid, then Dispersion liquid is filtered, pretreatment diatomite is obtained, counts in parts by weight, by 20 parts pre-process diatomite, 20 parts of graphene oxides, 80 Part paraffin, 20 parts of sodium bicarbonates are placed in ball milling mixing in ball mill, cross the sieve of 100 mesh to get modification infusorial earth;In parts by weight Meter, by 30 parts of aggregates, the dopamine solution that 20 parts of mass concentrations are 2.5mg/mL, 5 parts of biogas slurries, 40 parts of mass fractions are 0.5% Glucose solution is placed in fermentation cauldron, is 32 DEG C in temperature, under the conditions of rotating speed is 600r/min, mixed fermentation 5 days must ferment Liquid obtains filter cake then by filtering fermentation liquor, and filter cake is then placed in drying in vacuum freezing drying oven, obtains pretreatment aggregate;It presses Parts by weight meter, by 60 parts of cement, 60 parts of pretreatment aggregates, 20 parts of modification infusorial earths, 20 parts of clays, 20 parts of forsterite powder, 20 parts of organic siliconresins, 8 parts of water-reducing agents, 8 parts of silane coupling agents, 8 parts of surfactants, 20 parts of alkalescent phenol resins, 5 parts of solidifications Agent, 80 parts of water are placed in batch mixer, and under the conditions of rotating speed is 500r/min, it is anti-to get pleat-free cement base to be stirred 60min Water paint.The aggregate is river sand, mountain sand, sea sand, any one in aggregate chips or waste residue sand.The cement is silicate cement Any one in mud, aluminate cement or sulfate cement.The organic siliconresin is methyl trichlorosilane, dimethyl dichloro Any one in silane or phenyl trichlorosilane.The water-reducing agent is sodium lignin sulfonate, TH-928 poly carboxylic acid series water reducers Or any one in YZ-1 naphthalene series high-efficiency water-reducing agents.The silane coupling agent is silane resin acceptor kh-550, silane coupling agent Any one in KH-560 or Silane coupling reagent KH-570.The surfactant is polyethylene glycol, alkyl glycosides or 12 Any one of sodium alkyl benzene sulfonate.The curing agent is diethylenetriamine, arbitrary in triethylene tetramine or dipropylenetriamine It is a kind of.
Example 2
It counts in parts by weight, the glyoxal solution for being 40% by 40 parts of mass fractions, the potassium hydroxide that 20 parts of mass fractions are 30% Solution, 40 parts of hydroquinones are placed in four-hole boiling flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, Yu Wen Degree is 78 DEG C, and under the conditions of rotating speed is 500r/min, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, then to The ethylene urea of 0.3 times of glyoxal solution volume is added in four-hole boiling flask, in temperature be 62 DEG C, under the conditions of rotating speed is 500r/min, After constant temperature is stirred to react 60min, temperature in four-hole boiling flask is down to 52 DEG C, glyoxal solution body is then added into four-hole boiling flask The Silane coupling reagent KH-570 of 0.2 times of product is 52 DEG C in temperature, and under the conditions of rotating speed is 500r/min, constant temperature is stirred to react Temperature in four-hole boiling flask is down to 42 DEG C by 50min, is 42 DEG C in temperature, under the conditions of rotating speed is 500r/min, is continued constant temperature stirring 30min is reacted to get alkalescent phenol resin;By diatomite and butyl titanate in mass ratio 1:50 are placed in No. 1 beaker, and will No. 1 beaker is placed in ultrasonic disperse instrument, under the conditions of supersonic frequency is 75kHz, is mixed ultrasonic disperse 60min, is obtained dispersion liquid, then Dispersion liquid is filtered, pretreatment diatomite is obtained, counts in parts by weight, by 20 parts pre-process diatomite, 20 parts of graphene oxides, 80 Part paraffin, 20 parts of sodium bicarbonates are placed in ball milling mixing in ball mill, cross the sieve of 100 mesh to get modification infusorial earth;In parts by weight Meter, by 60 parts of cement, 20 parts of modification infusorial earths, 20 parts of clays, 20 parts of forsterite powder, 20 parts of organic siliconresins, 8 parts of diminishings Agent, 8 parts of silane coupling agents, 8 parts of surfactants, 20 parts of alkalescent phenol resins, 5 parts of curing agent, 80 parts of water are placed in batch mixer, Under the conditions of rotating speed is 500r/min, 60min is stirred to get pleat-free cement-base waterproof coating.The aggregate is river sand, Any one in mountain sand, sea sand, aggregate chips or waste residue sand.The cement is portland cement, aluminate cement or sulfuric acid brine Any one in mud.The organic siliconresin is methyl trichlorosilane, in dimethyldichlorosilane or phenyl trichlorosilane Any one.The water-reducing agent is sodium lignin sulfonate, in TH-928 poly carboxylic acid series water reducers or YZ-1 naphthalene series high-efficiency water-reducing agents Any one.The silane coupling agent is silane resin acceptor kh-550, silane coupling agent KH-560 or silane coupling agent KH- Any one in 570.The surfactant is polyethylene glycol, alkyl glycosides or neopelex it is any one Kind.The curing agent is diethylenetriamine, any one in triethylene tetramine or dipropylenetriamine.
Example 3
It counts in parts by weight, the glyoxal solution for being 40% by 40 parts of mass fractions, the potassium hydroxide that 20 parts of mass fractions are 30% Solution, 40 parts of hydroquinones are placed in four-hole boiling flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, Yu Wen Degree is 78 DEG C, and under the conditions of rotating speed is 500r/min, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, then to The ethylene urea of 0.3 times of glyoxal solution volume is added in four-hole boiling flask, in temperature be 62 DEG C, under the conditions of rotating speed is 500r/min, After constant temperature is stirred to react 60min, temperature in four-hole boiling flask is down to 52 DEG C, glyoxal solution body is then added into four-hole boiling flask The Silane coupling reagent KH-570 of 0.2 times of product is 52 DEG C in temperature, and under the conditions of rotating speed is 500r/min, constant temperature is stirred to react Temperature in four-hole boiling flask is down to 42 DEG C by 50min, is 42 DEG C in temperature, under the conditions of rotating speed is 500r/min, is continued constant temperature stirring 30min is reacted to get alkalescent phenol resin;It counts in parts by weight, by 30 parts of aggregates, 20 parts of mass concentrations are the more of 2.5mg/mL Bar amine aqueous solution, 5 parts of biogas slurries, the glucose solution that 40 parts of mass fractions are 0.5% are placed in fermentation cauldron, in temperature be 32 DEG C, rotating speed Under the conditions of 600r/min, mixed fermentation 5 days obtains zymotic fluid, then by filtering fermentation liquor, obtains filter cake, is then placed in filter cake It is dry in vacuum freezing drying oven, obtain pretreatment aggregate;It counts in parts by weight, by 60 parts of cement, 60 parts of pretreatment aggregates, 20 parts Clay, 20 parts of forsterite powder, 20 parts of organic siliconresins, 8 parts of water-reducing agents, 8 parts of silane coupling agents, 8 parts of surfactants, 20 parts Alkalescent phenol resin, 5 parts of curing agent, 80 parts of water are placed in batch mixer, under the conditions of rotating speed is 500r/min, are stirred 60min is to get pleat-free cement-base waterproof coating.The aggregate is river sand, mountain sand, and sea sand is arbitrary in aggregate chips or waste residue sand It is a kind of.The cement is portland cement, any one in aluminate cement or sulfate cement.The organic siliconresin is Any one in methyl trichlorosilane, dimethyldichlorosilane or phenyl trichlorosilane.The water-reducing agent is lignin sulfonic acid Any one in sodium, TH-928 poly carboxylic acid series water reducers or YZ-1 naphthalene series high-efficiency water-reducing agents.The silane coupling agent is silane Any one in coupling agent KH-550, silane coupling agent KH-560 or Silane coupling reagent KH-570.The surfactant is Any one of polyethylene glycol, alkyl glycosides or neopelex.The curing agent is diethylenetriamine, triethylene four Any one in amine or dipropylenetriamine.
Example 4
It counts in parts by weight, the glyoxal solution for being 40% by 40 parts of mass fractions, the potassium hydroxide that 20 parts of mass fractions are 30% Solution, 40 parts of hydroquinones are placed in four-hole boiling flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, Yu Wen Degree is 78 DEG C, and under the conditions of rotating speed is 500r/min, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, then to The ethylene urea of 0.3 times of glyoxal solution volume is added in four-hole boiling flask, in temperature be 62 DEG C, under the conditions of rotating speed is 500r/min, After constant temperature is stirred to react 60min, temperature in four-hole boiling flask is down to 52 DEG C, glyoxal solution body is then added into four-hole boiling flask The Silane coupling reagent KH-570 of 0.2 times of product is 52 DEG C in temperature, and under the conditions of rotating speed is 500r/min, constant temperature is stirred to react Temperature in four-hole boiling flask is down to 42 DEG C by 50min, is 42 DEG C in temperature, under the conditions of rotating speed is 500r/min, is continued constant temperature stirring 30min is reacted to get alkalescent phenol resin;By diatomite and butyl titanate in mass ratio 1:50 are placed in No. 1 beaker, and will No. 1 beaker is placed in ultrasonic disperse instrument, under the conditions of supersonic frequency is 75kHz, is mixed ultrasonic disperse 60min, is obtained dispersion liquid, then Dispersion liquid is filtered, pretreatment diatomite is obtained, counts in parts by weight, by 20 parts pre-process diatomite, 20 parts of graphene oxides, 80 Part paraffin, 20 parts of sodium bicarbonates are placed in ball milling mixing in ball mill, cross the sieve of 100 mesh to get modification infusorial earth;In parts by weight Meter, by 30 parts of aggregates, the dopamine solution that 20 parts of mass concentrations are 2.5mg/mL, 5 parts of biogas slurries, 40 parts of mass fractions are 0.5% Glucose solution is placed in fermentation cauldron, is 32 DEG C in temperature, under the conditions of rotating speed is 600r/min, mixed fermentation 5 days must ferment Liquid obtains filter cake then by filtering fermentation liquor, and filter cake is then placed in drying in vacuum freezing drying oven, obtains pretreatment aggregate;It presses Parts by weight meter, by 60 parts of cement, 60 parts of pretreatment aggregates, 20 parts of modification infusorial earths, 20 parts of forsterite powder, 20 parts of organosilicons Resin, 8 parts of water-reducing agents, 8 parts of silane coupling agents, 8 parts of surfactants, 20 parts of alkalescent phenol resins, 5 parts of curing agent, 80 parts of water It is placed in batch mixer, under the conditions of rotating speed is 500r/min, is stirred 60min to get pleat-free cement-base waterproof coating.Institute It is river sand to state aggregate, mountain sand, sea sand, any one in aggregate chips or waste residue sand.The cement is portland cement, aluminic acid brine Any one in mud or sulfate cement.The organic siliconresin is methyl trichlorosilane, dimethyldichlorosilane or phenyl Any one in trichlorosilane.The water-reducing agent is sodium lignin sulfonate, TH-928 poly carboxylic acid series water reducers or YZ-1 naphthalenes system Any one in high efficiency water reducing agent.The silane coupling agent is silane resin acceptor kh-550, silane coupling agent KH-560 or silicon Any one in alkane coupling agent kh-570.The surfactant is polyethylene glycol, alkyl glycosides or dodecyl benzene sulfonic acid Any one of sodium.The curing agent is diethylenetriamine, any one in triethylene tetramine or dipropylenetriamine.
Example 5
It counts in parts by weight, the glyoxal solution for being 40% by 40 parts of mass fractions, the potassium hydroxide that 20 parts of mass fractions are 30% Solution, 40 parts of hydroquinones are placed in four-hole boiling flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, Yu Wen Degree is 78 DEG C, and under the conditions of rotating speed is 500r/min, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, then to The ethylene urea of 0.3 times of glyoxal solution volume is added in four-hole boiling flask, in temperature be 62 DEG C, under the conditions of rotating speed is 500r/min, After constant temperature is stirred to react 60min, temperature in four-hole boiling flask is down to 52 DEG C, glyoxal solution body is then added into four-hole boiling flask The Silane coupling reagent KH-570 of 0.2 times of product is 52 DEG C in temperature, and under the conditions of rotating speed is 500r/min, constant temperature is stirred to react Temperature in four-hole boiling flask is down to 42 DEG C by 50min, is 42 DEG C in temperature, under the conditions of rotating speed is 500r/min, is continued constant temperature stirring 30min is reacted to get alkalescent phenol resin;By diatomite and butyl titanate in mass ratio 1:50 are placed in No. 1 beaker, and will No. 1 beaker is placed in ultrasonic disperse instrument, under the conditions of supersonic frequency is 75kHz, is mixed ultrasonic disperse 60min, is obtained dispersion liquid, then Dispersion liquid is filtered, pretreatment diatomite is obtained, counts in parts by weight, by 20 parts pre-process diatomite, 20 parts of graphene oxides, 80 Part paraffin, 20 parts of sodium bicarbonates are placed in ball milling mixing in ball mill, cross the sieve of 100 mesh to get modification infusorial earth;In parts by weight Meter, by 30 parts of aggregates, the dopamine solution that 20 parts of mass concentrations are 2.5mg/mL, 5 parts of biogas slurries, 40 parts of mass fractions are 0.5% Glucose solution is placed in fermentation cauldron, is 32 DEG C in temperature, under the conditions of rotating speed is 600r/min, mixed fermentation 5 days must ferment Liquid obtains filter cake then by filtering fermentation liquor, and filter cake is then placed in drying in vacuum freezing drying oven, obtains pretreatment aggregate;It presses Parts by weight meter, by 60 parts of cement, 60 parts of pretreatment aggregates, 20 parts of modification infusorial earths, 20 parts of clays, 20 parts of organic siliconresins, 8 Part water-reducing agent, 8 parts of silane coupling agents, 8 parts of surfactants, 20 parts of alkalescent phenol resins, 5 parts of curing agent, 80 parts of water are placed in mixed In material machine, under the conditions of rotating speed is 500r/min, 60min is stirred to get pleat-free cement-base waterproof coating.The aggregate For river sand, mountain sand, sea sand, any one in aggregate chips or waste residue sand.The cement is portland cement, aluminate cement or sulphur Any one in acid salt cement.The organic siliconresin is methyl trichlorosilane, dimethyldichlorosilane or phenyl trichlorine silicon Any one in alkane.The water-reducing agent is sodium lignin sulfonate, and TH-928 poly carboxylic acid series water reducers or YZ-1 naphthalene series high-efficiencies subtract Any one in aqua.The silane coupling agent is silane resin acceptor kh-550, silane coupling agent KH-560 or silane coupled Any one in agent KH-570.The surfactant is times of polyethylene glycol, alkyl glycosides or neopelex Meaning is a kind of.The curing agent is diethylenetriamine, any one in triethylene tetramine or dipropylenetriamine.
Example 6
It counts in parts by weight, the glyoxal solution for being 40% by 40 parts of mass fractions, the potassium hydroxide that 20 parts of mass fractions are 30% Solution, 40 parts of hydroquinones are placed in four-hole boiling flask, and four-hole boiling flask is placed in digital display and is tested the speed in constant temperature blender with magnetic force, Yu Wen Degree is 78 DEG C, and under the conditions of rotating speed is 500r/min, after constant temperature is stirred to react 4h, temperature in four-hole boiling flask is down to 62 DEG C, then to The ethylene urea of 0.3 times of glyoxal solution volume is added in four-hole boiling flask, in temperature be 62 DEG C, under the conditions of rotating speed is 500r/min, After constant temperature is stirred to react 60min, temperature in four-hole boiling flask is down to 52 DEG C, glyoxal solution body is then added into four-hole boiling flask The Silane coupling reagent KH-570 of 0.2 times of product is 52 DEG C in temperature, and under the conditions of rotating speed is 500r/min, constant temperature is stirred to react Temperature in four-hole boiling flask is down to 42 DEG C by 50min, is 42 DEG C in temperature, under the conditions of rotating speed is 500r/min, is continued constant temperature stirring 30min is reacted to get alkalescent phenol resin;By diatomite and butyl titanate in mass ratio 1:50 are placed in No. 1 beaker, and will No. 1 beaker is placed in ultrasonic disperse instrument, under the conditions of supersonic frequency is 75kHz, is mixed ultrasonic disperse 60min, is obtained dispersion liquid, then Dispersion liquid is filtered, pretreatment diatomite is obtained, counts in parts by weight, by 20 parts pre-process diatomite, 20 parts of graphene oxides, 80 Part paraffin, 20 parts of sodium bicarbonates are placed in ball milling mixing in ball mill, cross the sieve of 100 mesh to get modification infusorial earth;In parts by weight Meter, by 30 parts of aggregates, the dopamine solution that 20 parts of mass concentrations are 2.5mg/mL, 5 parts of biogas slurries, 40 parts of mass fractions are 0.5% Glucose solution is placed in fermentation cauldron, is 32 DEG C in temperature, under the conditions of rotating speed is 600r/min, mixed fermentation 5 days must ferment Liquid obtains filter cake then by filtering fermentation liquor, and filter cake is then placed in drying in vacuum freezing drying oven, obtains pretreatment aggregate;It presses Parts by weight meter, by 60 parts of cement, 60 parts of pretreatment aggregates, 20 parts of modification infusorial earths, 20 parts of clays, 20 parts of forsterite powder, 8 Part water-reducing agent, 8 parts of silane coupling agents, 8 parts of surfactants, 20 parts of alkalescent phenol resins, 5 parts of curing agent, 80 parts of water are placed in mixed In material machine, under the conditions of rotating speed is 500r/min, 60min is stirred to get pleat-free cement-base waterproof coating.The aggregate For river sand, mountain sand, sea sand, any one in aggregate chips or waste residue sand.The cement is portland cement, aluminate cement or sulphur Any one in acid salt cement.The water-reducing agent is sodium lignin sulfonate, TH-928 poly carboxylic acid series water reducers or YZ-1 naphthalenes system Any one in high efficiency water reducing agent.The silane coupling agent is silane resin acceptor kh-550, silane coupling agent KH-560 or silicon Any one in alkane coupling agent kh-570.The surfactant is polyethylene glycol, alkyl glycosides or dodecyl benzene sulfonic acid Any one of sodium.The curing agent is diethylenetriamine, any one in triethylene tetramine or dipropylenetriamine.
Comparative example:The cement-base waterproof coating of architectural waterproof material Manufacturing Co., Ltd of Yantai City production.
A kind of pleat-free cement-base waterproof coating of example 1 to the gained of example 6 and comparative example product are subjected to performance detection, Specific detection method is as follows:
1. anti-permeability performance:It is tested according to JG/T193 and ASTMD5084, and calculation permeability coefficient;
2. compression strength:It is tested according to GB/T50081;
3. tensile splitting strength:It is tested according to GB/T50081;
4. flexural strength:It is tested according to GB/T50081.
Specific testing result is as shown in table 1:
Table 1:The specific testing result of pleat-free cement-base waterproof coating performance
By 1 testing result of table it is found that a kind of pleat-free cement-base waterproof coating of technical solution of the present invention preparation is with waterproof Property good, tensile strength is high, High anti bending strength, tensile splitting strength are high feature, have in the development of building material industry wide Wealthy foreground.

Claims (9)

1. a kind of preparation method of pleat-free cement-base waterproof coating, it is characterised in that specific preparation process is as follows:
(1)By diatomite and butyl titanate in mass ratio 1:30~1:50 mixing ultrasounds, filtering obtain pretreatment diatomite, press Parts by weight meter pre-processes diatomite, 10~20 parts of graphene oxides, 60~80 parts of paraffin, 10~20 parts of carbon by 10~20 parts Sour hydrogen sodium ball milling mixing is sieved to get modification infusorial earth;
(2)It counts in parts by weight, by 20~30 parts of aggregates, 10~20 parts of dopamine solutions, 3~5 parts of biogas slurries, 30~40 portions of grapes Sugar juice ferments, and filters, dry, obtains pretreatment aggregate;
(3)It counts in parts by weight, by 50~60 parts of cement, 50~60 parts of pretreatment aggregates, 10~20 parts of modification infusorial earths, 10~ 20 parts of clays, 10~20 parts of forsterite powder, 10~20 parts of organic siliconresins, 5~8 parts of water-reducing agents, 5~8 parts of silane coupling agents, 5~8 parts of surfactants, 10~20 parts of alkalescent phenol resins, 3~5 parts of curing agent, 60~80 parts of water are stirred to get anti- Fold-type cement-base waterproof coating.
2. a kind of preparation method of pleat-free cement-base waterproof coating according to claim 1, it is characterised in that:Step(2) The aggregate is river sand, mountain sand, sea sand, any one in aggregate chips or waste residue sand.
3. a kind of preparation method of pleat-free cement-base waterproof coating according to claim 1, it is characterised in that:Step(3) The cement is portland cement, any one in aluminate cement or sulfate cement.
4. a kind of preparation method of pleat-free cement-base waterproof coating according to claim 1, it is characterised in that:Step(3) The organic siliconresin is methyl trichlorosilane, any one in dimethyldichlorosilane or phenyl trichlorosilane.
5. a kind of preparation method of pleat-free cement-base waterproof coating according to claim 1, it is characterised in that:Step(3) The water-reducing agent is sodium lignin sulfonate, any one in TH-928 poly carboxylic acid series water reducers or YZ-1 naphthalene series high-efficiency water-reducing agents Kind.
6. a kind of preparation method of pleat-free cement-base waterproof coating according to claim 1, it is characterised in that:Step(3) The silane coupling agent is silane resin acceptor kh-550, any one in silane coupling agent KH-560 or Silane coupling reagent KH-570 Kind.
7. a kind of preparation method of pleat-free cement-base waterproof coating according to claim 1, it is characterised in that:Step(3) The surfactant is any one of polyethylene glycol, alkyl glycosides or neopelex.
8. a kind of preparation method of pleat-free cement-base waterproof coating according to claim 1, it is characterised in that:Step(3) The preparation process of the alkalescent phenol resin is:It counts in parts by weight, by 30~40 parts of glyoxal solutions, 10~20 parts of hydroxides Potassium solution, 30~40 parts of hydroquinone constant temperature are stirred to react, and the ethylene urea of 0.2~0.3 times of glyoxal solution volume is added in cooling It is stirred to react, cools down, the Silane coupling reagent KH-570 that 0.1~0.2 times of glyoxal solution volume is added is stirred to react, and is cooled down, i.e., Obtain alkalescent phenol resin.
9. a kind of preparation method of pleat-free cement-base waterproof coating according to claim 1, it is characterised in that:Step(3) The curing agent is diethylenetriamine, any one in triethylene tetramine or dipropylenetriamine.
CN201810355075.XA 2018-04-19 2018-04-19 A kind of preparation method of pleat-free cement-base waterproof coating Pending CN108424082A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810355075.XA CN108424082A (en) 2018-04-19 2018-04-19 A kind of preparation method of pleat-free cement-base waterproof coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810355075.XA CN108424082A (en) 2018-04-19 2018-04-19 A kind of preparation method of pleat-free cement-base waterproof coating

Publications (1)

Publication Number Publication Date
CN108424082A true CN108424082A (en) 2018-08-21

Family

ID=63161409

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810355075.XA Pending CN108424082A (en) 2018-04-19 2018-04-19 A kind of preparation method of pleat-free cement-base waterproof coating

Country Status (1)

Country Link
CN (1) CN108424082A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109400098A (en) * 2018-11-19 2019-03-01 吴广义 A kind of environment-friendly type water-proof plugging material and preparation method and application
CN109627739A (en) * 2018-10-29 2019-04-16 万玉梅 A kind of preparation method of water-proof leak preventer
CN113461418A (en) * 2021-07-21 2021-10-01 辽宁科技大学 Slag corrosion resistant coating for carbon-free ladle lining and preparation method thereof
CN116003040A (en) * 2023-02-28 2023-04-25 辽宁工业大学 High-performance cement-based composite material containing reduced graphene oxide coated sand and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105669099A (en) * 2015-12-31 2016-06-15 富思特新材料科技发展股份有限公司 Aqueous epoxy coating for terraces, and preparation method thereof
CN105731933A (en) * 2016-03-01 2016-07-06 青岛华高墨烯科技股份有限公司 Preparation method of graphene oxide/high-strength concrete composite material
CN106634154A (en) * 2016-12-19 2017-05-10 四川嘉宝莉涂料有限公司 Stabilization method of diatomite/nanometer TiO2 photocatalytic paint additive
CN106830819A (en) * 2016-12-29 2017-06-13 中冶建筑研究总院有限公司 Cement base molding material and preparation method thereof
CN107382218A (en) * 2017-08-31 2017-11-24 常州富思通管道有限公司 A kind of modified EPS concrete

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105669099A (en) * 2015-12-31 2016-06-15 富思特新材料科技发展股份有限公司 Aqueous epoxy coating for terraces, and preparation method thereof
CN105731933A (en) * 2016-03-01 2016-07-06 青岛华高墨烯科技股份有限公司 Preparation method of graphene oxide/high-strength concrete composite material
CN106634154A (en) * 2016-12-19 2017-05-10 四川嘉宝莉涂料有限公司 Stabilization method of diatomite/nanometer TiO2 photocatalytic paint additive
CN106830819A (en) * 2016-12-29 2017-06-13 中冶建筑研究总院有限公司 Cement base molding material and preparation method thereof
CN107382218A (en) * 2017-08-31 2017-11-24 常州富思通管道有限公司 A kind of modified EPS concrete

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
周莹: "《有机化学实验》", 28 February 2003, 湖南大学出版社 *
韩长日等: "《橡塑助剂生产工艺与技术》", 30 November 2015, 科学技术文献出版社 *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109627739A (en) * 2018-10-29 2019-04-16 万玉梅 A kind of preparation method of water-proof leak preventer
CN109400098A (en) * 2018-11-19 2019-03-01 吴广义 A kind of environment-friendly type water-proof plugging material and preparation method and application
CN109400098B (en) * 2018-11-19 2020-12-22 吴广义 Environment-friendly waterproof plugging material, preparation method and application
CN113461418A (en) * 2021-07-21 2021-10-01 辽宁科技大学 Slag corrosion resistant coating for carbon-free ladle lining and preparation method thereof
CN113461418B (en) * 2021-07-21 2022-09-16 辽宁科技大学 Slag corrosion resistant coating for carbon-free ladle lining and preparation method thereof
CN116003040A (en) * 2023-02-28 2023-04-25 辽宁工业大学 High-performance cement-based composite material containing reduced graphene oxide coated sand and preparation method thereof
CN116003040B (en) * 2023-02-28 2023-07-07 辽宁工业大学 High-performance cement-based composite material containing reduced graphene oxide coated sand and preparation method thereof

Similar Documents

Publication Publication Date Title
CN108424082A (en) A kind of preparation method of pleat-free cement-base waterproof coating
CN107540304B (en) Composite cement-based capillary crystalline waterproof material
CN114591049B (en) Method for preparing green mortar by using construction waste
CN108164208A (en) A kind of nano silicon dioxide regeneration concrete and preparation method thereof
CN104402350B (en) Earth building material modification method and the method that building block is prepared using the modified raw-soil
CN107540285B (en) Method for preparing finely ground glass powder building mortar by using waste oyster shells
CN111393101A (en) Pervious concrete and preparation method thereof
CN109970405A (en) A kind of concrete and preparation method thereof
CN110183193A (en) A kind of super-early strength cement base does not disperse patching material and preparation method thereof under water
CN103408273A (en) Permeable-adhesive type cement-based sealing and repairing agent and preparation method thereof
CN108358591A (en) Building material compositions and preparation method thereof containing drift-sand
CN110092623A (en) A kind of dredging and reclamation silt curing agent
CN104628354A (en) Nano modified self-penetrating water-based repair material and preparation method thereof
CN108623228A (en) A kind of seawater corrosion resistance inorganic structure fluid sealant and preparation method thereof
CN109135377A (en) A kind of preparation method of curing compound
CN108328995A (en) A kind of preparation method of waterproof mortar
CN112551837A (en) Silt curing agent based on induced calcification of high-molecular polysaccharide
CN112279571A (en) Anti-freezing concrete and preparation method thereof
CN115286286B (en) Efficient water reducing agent for concrete and preparation method thereof
CN106587841A (en) High-ductility cement based composite material and preparation method thereof
Liu et al. Analysis on pore structure of non-dispersible underwater concrete in saline soil area
CN106495603B (en) A kind of preparation method of weather-proof cement-base waterproof coating
CN112299774A (en) Water permeable brick and preparation process thereof
CN110041036A (en) A kind of alkali-activated carbonatite concrete material being specially adapted for underwater casting
CN106630902B (en) A kind of strong concrete and preparation method thereof

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
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20180821