CN107500609A - A kind of resistant to sea water corrodes the non-burning brick preparation method of acidproof slag micropowder and clay - Google Patents
A kind of resistant to sea water corrodes the non-burning brick preparation method of acidproof slag micropowder and clay Download PDFInfo
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- CN107500609A CN107500609A CN201710792112.9A CN201710792112A CN107500609A CN 107500609 A CN107500609 A CN 107500609A CN 201710792112 A CN201710792112 A CN 201710792112A CN 107500609 A CN107500609 A CN 107500609A
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- 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
- C04B26/00—Compositions of mortars, concrete or artificial stone, containing only organic binders, e.g. polymer or resin concrete
- C04B26/02—Macromolecular compounds
- C04B26/10—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C04B26/16—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4202—Two or more polyesters of different physical or chemical nature
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4236—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
- C08G18/4238—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6633—Compounds of group C08G18/42
- C08G18/6637—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/664—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
- C08G18/6644—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203 having at least three hydroxy groups
-
- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00241—Physical properties of the materials not provided for elsewhere in C04B2111/00
- C04B2111/00293—Materials impermeable to liquids
-
- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/20—Resistance against chemical, physical or biological attack
- C04B2111/24—Sea water resistance
-
- 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
- C04B2201/00—Mortars, concrete or artificial stone characterised by specific physical values
- C04B2201/50—Mortars, concrete or artificial stone characterised by specific physical values for the mechanical strength
Abstract
A kind of resistant to sea water corrodes the non-burning brick preparation method of acidproof slag micropowder and clay, and slag micropowder is placed in mixed liquor, stirs, 300 DEG C of thermophilic digestion mixed liquors, 1 as a child, filtering, slag micropowder is taken out, is mixed with clay, the water for adding 50% deal continues stirring and obtains compound;Compound is obtained into adobe through vibration moulding, Superfine slag powder baking-free brick is obtained after the maintenance of adobe normal temperature.Such a property slag micropowder mixes non-burning brick with clay, while non-burning brick combination property is improved, reach reduction production cost, the purpose of energy-saving and emission-reduction, once it is widely used in non-burning brick production, it will bring good economic benefit and social benefit, simultaneously, by rubber powder infiltration in micro mist, the later stage it is not non-burning brick, meet water after, strongly adherent material, fragment of brick bulk strength obtains bigger lifting, while can effectively improve the resistant to sea water etch performance of cement concrete, especially suitable for resistant to sea water engineering.
Description
Technical field:
The present invention relates to the non-burning brick preparation that a kind of resistant to sea water of building material field corrodes acidproof slag micropowder and clay
Method.
Background technology:
Building engineering construction efficiency can be improved using cement and concrete product, after concrete cast, if hot climate,
It is air-dried, is conserved not in time, the evaporation of concrete reclaimed water branch is too fast, forms dehydrating phenomena, can make to have formed gelinite
Cement granules can not abundant aquation, it is impossible to be converted into stable crystallization, lack enough cohesive forces, so as to can be in concrete table
There is sheet in face or powdery comes off, in addition, when concrete not yet possesses enough intensity, the too early evaporation of moisture can also produce
, there is cup shake in larger contraction distortion, influences the durability and globality of concrete.Therefore increase in concrete strength
Phase, in order to obtain enough intensity within a short period of time and accelerate mould turnover, while ensure the intensity of concrete, durability etc.
Technical indicator, generally it is conserved.Traditional concrete curing method has natural curing, atmospheric steam curing and high temperature high
Pressure maintenance etc..It is longer the time required to natural curing, and quality is difficult to ensure that;Scientific and reasonable steam curing system in atmospheric steam curing
It is to produce one of important prerequisite of high quality cement concrete product with technique, maintaining process, which is generally divided into, quiet to stop, heats up, be permanent
Temperature, 4 stages of cooling, in order to prevent product from causing concrete to produce crack because internal-external temperature difference is excessive or thermostat temperature is too high,
Must strictly control it is steam-cured during heating-cooling speed and thermostat temperature etc., process very complicated and require strict, condition control
Make and bad be easy for causing concrete product not reach preparation technology requirement;And HTHP curing condition requires higher, lead to
Often critical shortage, its exacting terms limit its application to the various resources in many construction places.
The defects of conventional method, is increasingly difficult in adapt to modern construction needs, and therefore, people investigated concrete and support
The new material and technique of shield, granulated blast-furnace slag are blast-furnace cinders by a kind of with very high potential obtained from the chilling of water
The vitreous structure material of activity, slag micropowder, slag fibre, builds the road in slag cements, concrete admixture in recent years
Filler etc. obtains very big utilization, and the enhancing of concrete and rebar cohesive force, late strength of concrete mixed with slag micropowder carry
The high, good characteristics such as prevent shrinkage cracking, concrete basicity low, are the stocks for preparing high performance concrete, 2011 years
China's iron and steel output reaches more than 68.3 hundred million tons, can discharge nearly 2,000,000,000 tons of granulated blast-furnace slag, the money of granulated blast-furnace slag
Sourceization can also greatly reduce occupation of land and environmental pollution using the energy is saved while reducing production cost, produce preferably warp
Benefit of helping and social benefit.Although the research of slag micropowder improves the concrete performances such as intensity, workability, cohesive force, from
Do not improved angularly from the resources conservation such as steam curing time and condition, the input of high-tension apparatus, production efficiency.How to enter
One step improve the lateral reactivity of slag micropowder, increase its feature, to expand its application field critically important as one in industry
Research topic.
The content of the invention:
The technical problems to be solved by the invention are the defects of part takes prior art, there is provided a kind of resistant to sea water corrodes acidproof
The non-burning brick preparation method of slag micropowder and clay.
The technical problems to be solved by the invention are realized using following technical scheme.
A kind of resistant to sea water corrodes the non-burning brick preparation method of acidproof slag micropowder and clay, it is characterised in that:Slag is micro-
Powder is placed in mixed liquor, and stirring, 300 DEG C of thermophilic digestion mixed liquors, 1 as a child, filtering, is taken out slag micropowder, is mixed with clay
Stirring, the water for adding 50% deal continue stirring and obtain compound;
Compound is obtained into adobe through vibration moulding, Superfine slag powder baking-free brick is obtained after the maintenance of adobe normal temperature;
Comprise the following steps that:
Take modified epoxy add reactor in, stirring be warming up to 85 DEG C, then be added dropwise acrylic acid, epoxychloropropane and
The mixed liquor of hydroquinones, stirring reaction 4-5 hours, obtain preformed objects A;
Take talcum powder to add in reactor, be heated to 130 DEG C when stirring vacuumizes and be incubated 1h;It is subsequently cooled to 80
DEG C, into reactor, dropwise addition titanium dioxide is incubated while stirring, and 90 DEG C are progressively warming up to after being added dropwise and is incubated 2 hours, cold
But discharge, obtain preformed objects B;
Preformed objects A and preformed objects B are put into distilling apparatus, carry out vacuum exhaust using vavuum pump so that distilling apparatus
Vacuum reaches about 0.6-1Pa, opens heater and heats heater block and condensing part respectively so that the temperature of heater block
Degree is maintained at 550-600 DEG C, and the temperature of condensing part is maintained at 320-340 DEG C, continuous vacuum distillation 5-6 hours;
After vacuum distillation terminates, distillate is collected, adds curing agent, silane coupler, stirs 5~6 minutes, then adds
Quartz sand and liquid low-molecular polyamide, stir 20~22 minutes, add organosilicon acrylic resin emulsion, stir 9~10 minutes, most
After add thickener, be stirred for 10~12 minutes, be then filled into bucket, precipitate, collect upper liquid, obtain mixed liquor;
Mica powder, silica flour, carborundum powder, titanium dioxide zirconium powder and mild-clay powder are added sequentially to stir in mixer
3-5 minutes, it is well mixed, obtains mixed powder;
Solid after precipitation is collected, mixed with mixed powder, the mud added after impurity elimination, is stirred continuously, 1 times of amount of addition
Moisture, heated, at a temperature of 300 DEG C, after heating 2 minutes, add adhesive for polyurethane, stir 3-5 minutes, be well mixed
To clay,
Slag micropowder is placed in mixed liquor, stirred, 300 DEG C of thermophilic digestion mixed liquors, 1 as a child, filtering, takes out slag
Micro mist, mixed with clay, the water for adding 50% deal continues stirring and obtains compound;The ratio of slag micropowder and clay
For 9:1;
Compound is obtained into adobe through vibration moulding, Superfine slag powder baking-free brick is obtained after the maintenance of adobe normal temperature.
Each component content is respectively in above-mentioned steps:Modified epoxy 10-12 parts, acrylic acid 2-6 parts, epoxychloropropane
12-15 parts, hydroquinones 5-9 parts, talcum powder 5-8 parts, titanium dioxide 2-6 parts, curing agent 10-11 parts, silane coupler 5-6
Part, quartz sand 20-26 parts, liquid low-molecular polyamide 16-19 parts, organosilicon acrylic resin emulsion 20-30 parts, thickener 2-5 parts, cloud
Female powder 10-15 parts, silica flour 10-15 parts, carborundum powder 10-15 parts, titanium dioxide zirconium powder and mild-clay powder 10-15 parts, mud
5000-6000 parts, adhesive for polyurethane 50-60 parts.
Described adhesive for polyurethane is prepared including following components:
Ethylene glycol 30-35 parts, adipic acid 75-80 parts, ethyl acetate 5-20 parts, toluene di-isocyanate(TDI) 25-30 parts, acetic acid
Butyl ester 20-25 parts, trimethylolpropane 5-7 parts, polyester 5-7 parts.
Described adhesive for polyurethane, which comprises the following steps, to be prepared:
The preparation of polyadipate-ethylene glycol includes
1. ethylene glycol is put into reactor, heating stirring, while adipic acid is added, progressively heat up, heated up in 2 hours
To 200 DEG C;
2. when acid number reaches 35mgKOH/g, Depressor response kettle, 0.05Mpa, water outlet 8 hours are decompressed to;
3. when acid number reaches 15mgKOH/g, Depressor response kettle, 0.5Mpa is decompressed to, gone out when controlling acid number 2mgKOH/g
Material.
The preparation of modified poly ester includes
1. putting into 5 parts of butyl acetates in reactor, half an hour is stirred, polyester is added, is heated to 60 DEG C, adds 5 parts
Toluene di-isocyanate(TDI);
2. being warming up to 100-120 DEG C, ethyl acetate, mixed dissolution are added.
The preparation of modified isocyanate includes
1. adding remaining toluene di-isocyanate(TDI) and remaining butyl acetate in a kettle, stir;
2. add trimethylolpropane;
3. being heated to 70 DEG C, heat 1 hour;
4. it is cooled to room temperature.
After the completion of preparation, modified poly ester and modified isocyanate are mixed, proportion 100:20-50, addition polyadipate-
Ethylene glycol, 190 DEG C are warming up to, heating duration 1 hour, is condensed into 50-60 parts, you can obtain the polyurethane gluing of high bonding strength
Agent.
Described part is parts by weight.
In summary, such a property slag micropowder mixes non-burning brick with clay, is improving the same of non-burning brick combination property
When, reach reduction production cost, the purpose of energy-saving and emission-reduction, once being widely used in non-burning brick production, it will bring very
Good economic benefit and social benefit, meanwhile, by rubber powder infiltration in micro mist, the later stage it is not non-burning brick, after meeting water, strength is viscous
Addendum material, fragment of brick bulk strength obtain bigger lifting, can effectively improve the resistant to sea water etch performance of cement concrete, especially
Suitable for resistant to sea water engineering.
Embodiment:
In order that the technical means, the inventive features, the objects and the advantages of the present invention are easy to understand, tie below
Specific embodiment is closed, the present invention is expanded on further.
Specific embodiment 1:
A kind of resistant to sea water corrodes the non-burning brick preparation method of acidproof slag micropowder and clay, and slag micropowder is placed in into mixed liquor
In, stirring, 300 DEG C of thermophilic digestion mixed liquors, 1 as a child, filtering, takes out slag micropowder, mixes, adds with clay
The water of 50% deal continues stirring and obtains compound;
Compound is obtained into adobe through vibration moulding, Superfine slag powder baking-free brick is obtained after the maintenance of adobe normal temperature;
Comprise the following steps that:
Take modified epoxy add reactor in, stirring be warming up to 85 DEG C, then be added dropwise acrylic acid, epoxychloropropane and
The mixed liquor of hydroquinones, stirring reaction 4-5 hours, obtain preformed objects A;
Take talcum powder to add in reactor, be heated to 130 DEG C when stirring vacuumizes and be incubated 1h;It is subsequently cooled to 80
DEG C, into reactor, dropwise addition titanium dioxide is incubated while stirring, and 90 DEG C are progressively warming up to after being added dropwise and is incubated 2 hours, cold
But discharge, obtain preformed objects B;
Preformed objects A and preformed objects B are put into distilling apparatus, carry out vacuum exhaust using vavuum pump so that distilling apparatus
Vacuum reaches about 0.6-1Pa, opens heater and heats heater block and condensing part respectively so that the temperature of heater block
Degree is maintained at 550-600 DEG C, and the temperature of condensing part is maintained at 320-340 DEG C, continuous vacuum distillation 5-6 hours;
After vacuum distillation terminates, distillate is collected, adds curing agent, silane coupler, stirs 5~6 minutes, then adds
Quartz sand and liquid low-molecular polyamide, stir 20~22 minutes, add organosilicon acrylic resin emulsion, stir 9~10 minutes, most
After add thickener, be stirred for 10~12 minutes, be then filled into bucket, precipitate, collect upper liquid, obtain mixed liquor;
Mica powder, silica flour, carborundum powder, titanium dioxide zirconium powder and mild-clay powder are added sequentially to stir in mixer
3-5 minutes, it is well mixed, obtains mixed powder;
Solid after precipitation is collected, mixed with mixed powder, the mud added after impurity elimination, is stirred continuously, 1 times of amount of addition
Moisture, heated, at a temperature of 300 DEG C, after heating 2 minutes, add adhesive for polyurethane, stir 3-5 minutes, be well mixed
To clay,
Slag micropowder is placed in mixed liquor, stirred, 300 DEG C of thermophilic digestion mixed liquors, 1 as a child, filtering, takes out slag
Micro mist, mixed with clay, the water for adding 50% deal continues stirring and obtains compound;The ratio of slag micropowder and clay
For 9:1;
Compound is obtained into adobe through vibration moulding, Superfine slag powder baking-free brick is obtained after the maintenance of adobe normal temperature.
Each component content is respectively in above-mentioned steps:10 parts of modified epoxy, 2 parts of acrylic acid, 12 parts of epoxychloropropane,
5 parts of hydroquinones, 5 parts of talcum powder, 2 parts of titanium dioxide, 10 parts of curing agent, 5 parts of silane coupler, 20 parts of quartz sand, liquid are low
16 parts of molecular weight polyamide, 20 parts of organosilicon acrylic resin emulsion, 2 parts of thickener, 10 parts of mica powder, 10 parts of silica flour, carborundum powder 10
Part, titanium dioxide zirconium powder and 10 parts of mild-clay powder, 5000 parts of mud, 50 parts of adhesive for polyurethane.
Adhesive for polyurethane is prepared including following components:
30 parts of ethylene glycol, 75 parts of adipic acid, 5 parts of ethyl acetate, 25 parts of toluene di-isocyanate(TDI), 20 parts of butyl acetate, three
5 parts of hydroxymethyl-propane, 5 parts of polyester.
Adhesive for polyurethane, which comprises the following steps, to be prepared:
The preparation of polyadipate-ethylene glycol includes
4. ethylene glycol is put into reactor, heating stirring, while adipic acid is added, progressively heat up, heated up in 2 hours
To 200 DEG C;
5. when acid number reaches 35mgKOH/g, Depressor response kettle, 0.05Mpa, water outlet 8 hours are decompressed to;
6. when acid number reaches 15mgKOH/g, Depressor response kettle, 0.5Mpa is decompressed to, gone out when controlling acid number 2mgKOH/g
Material.
The preparation of modified poly ester includes
3. putting into 5 parts of butyl acetates in reactor, half an hour is stirred, polyester is added, is heated to 60 DEG C, adds 5 parts
Toluene di-isocyanate(TDI);
4. being warming up to 100-120 DEG C, ethyl acetate, mixed dissolution are added.
The preparation of modified isocyanate includes
5. adding remaining toluene di-isocyanate(TDI) and remaining butyl acetate in a kettle, stir;
6. add trimethylolpropane;
7. being heated to 70 DEG C, heat 1 hour;
8. it is cooled to room temperature.
After the completion of preparation, modified poly ester and modified isocyanate are mixed, proportion 100:20-50, addition polyadipate-
Ethylene glycol, 190 DEG C are warming up to, heating duration 1 hour, is condensed into 50 parts, you can obtain the adhesive for polyurethane of high bonding strength.
Part is parts by weight.
Existing baking-free slag brick is contrasted, is compared, intensity and water permeability resistance are contrasted, as follows:
Data understand that setting rate is accelerated, while can effectively improve the resistant to sea water etch performance of cement concrete, especially
Suitable for resistant to sea water engineering.
Embodiment 2:A kind of resistant to sea water corrodes the non-burning brick preparation method of acidproof slag micropowder and clay, and slag micropowder is put
In mixed liquor, stirring, 300 DEG C of thermophilic digestion mixed liquors, 1 as a child, filtering, takes out slag micropowder, is mixed with clay,
The water for adding 50% deal continues stirring and obtains compound;
Compound is obtained into adobe through vibration moulding, Superfine slag powder baking-free brick is obtained after the maintenance of adobe normal temperature;
Comprise the following steps that:
Take modified epoxy add reactor in, stirring be warming up to 85 DEG C, then be added dropwise acrylic acid, epoxychloropropane and
The mixed liquor of hydroquinones, stirring reaction 4-5 hours, obtain preformed objects A;
Take talcum powder to add in reactor, be heated to 130 DEG C when stirring vacuumizes and be incubated 1h;It is subsequently cooled to 80
DEG C, into reactor, dropwise addition titanium dioxide is incubated while stirring, and 90 DEG C are progressively warming up to after being added dropwise and is incubated 2 hours, cold
But discharge, obtain preformed objects B;
Preformed objects A and preformed objects B are put into distilling apparatus, carry out vacuum exhaust using vavuum pump so that distilling apparatus
Vacuum reaches about 0.6-1Pa, opens heater and heats heater block and condensing part respectively so that the temperature of heater block
Degree is maintained at 550-600 DEG C, and the temperature of condensing part is maintained at 320-340 DEG C, continuous vacuum distillation 5-6 hours;
After vacuum distillation terminates, distillate is collected, adds curing agent, silane coupler, stirs 5~6 minutes, then adds
Quartz sand and liquid low-molecular polyamide, stir 20~22 minutes, add organosilicon acrylic resin emulsion, stir 9~10 minutes, most
After add thickener, be stirred for 10~12 minutes, be then filled into bucket, precipitate, collect upper liquid, obtain mixed liquor;
Mica powder, silica flour, carborundum powder, titanium dioxide zirconium powder and mild-clay powder are added sequentially to stir in mixer
3-5 minutes, it is well mixed, obtains mixed powder;
Solid after precipitation is collected, mixed with mixed powder, the mud added after impurity elimination, is stirred continuously, 1 times of amount of addition
Moisture, heated, at a temperature of 300 DEG C, after heating 2 minutes, add adhesive for polyurethane, stir 3-5 minutes, be well mixed
To clay,
Slag micropowder is placed in mixed liquor, stirred, 300 DEG C of thermophilic digestion mixed liquors, 1 as a child, filtering, takes out slag
Micro mist, mixed with clay, the water for adding 50% deal continues stirring and obtains compound;The ratio of slag micropowder and clay
For 9:1;
Compound is obtained into adobe through vibration moulding, Superfine slag powder baking-free brick is obtained after the maintenance of adobe normal temperature.
Each component content is respectively in above-mentioned steps:12 parts of modified epoxy, 6 parts of acrylic acid, 15 parts of epoxychloropropane,
9 parts of hydroquinones, 8 parts of talcum powder, 6 parts of toluene di-isocyanate(TDI), 11 parts of curing agent, 6 parts of silane coupler, 26 parts of quartz sand,
19 parts of liquid low-molecular polyamide, 30 parts of organosilicon acrylic resin emulsion, 5 parts of thickener, 15 parts of mica powder, 15 parts of silica flour, carbonization
15 parts of 15 parts of silica flour, titanium dioxide zirconium powder and mild-clay powder, 6000 parts of mud, 60 parts of adhesive for polyurethane.
Adhesive for polyurethane is prepared including following components:
35 parts of ethylene glycol, 80 parts of adipic acid, 20 parts of ethyl acetate, 30 parts of toluene di-isocyanate(TDI), 25 parts of butyl acetate, three
7 parts of hydroxymethyl-propane, 7 parts of polyester.
Adhesive for polyurethane, which comprises the following steps, to be prepared:
The preparation of polyadipate-ethylene glycol includes
7. ethylene glycol is put into reactor, heating stirring, while adipic acid is added, progressively heat up, heated up in 2 hours
To 200 DEG C;
8. when acid number reaches 35mgKOH/g, Depressor response kettle, 0.05Mpa, water outlet 8 hours are decompressed to;
9. when acid number reaches 15mgKOH/g, Depressor response kettle, 0.5Mpa is decompressed to, gone out when controlling acid number 2mgKOH/g
Material.
The preparation of modified poly ester includes
5. putting into 5 parts of butyl acetates in reactor, half an hour is stirred, polyester is added, is heated to 60 DEG C, adds 5 parts
Toluene di-isocyanate(TDI);
6. being warming up to 100-120 DEG C, ethyl acetate, mixed dissolution are added.
The preparation of modified isocyanate includes
9. adding remaining toluene di-isocyanate(TDI) and remaining butyl acetate in a kettle, stir;
10. add trimethylolpropane;
70 DEG C are heated to, is heated 1 hour;
It is cooled to room temperature.
After the completion of preparation, modified poly ester and modified isocyanate are mixed, proportion 100:20-50, addition polyadipate-
Ethylene glycol, 190 DEG C are warming up to, heating duration 1 hour, is condensed into 60 parts, you can obtain the adhesive for polyurethane of high bonding strength.
Part is parts by weight.
Existing baking-free slag brick is contrasted, is compared, intensity and water permeability resistance are contrasted, as follows:
Data understand that setting rate is accelerated, while can effectively improve the resistant to sea water etch performance of cement concrete, especially
Suitable for resistant to sea water engineering.
General principle, principal character and the advantages of the present invention of the present invention has been shown and described above.The technology of the industry
Personnel are it should be appreciated that the present invention is not limited to the above embodiments, and the simply explanation described in above-described embodiment and specification is originally
The principle of invention, without departing from the spirit and scope of the present invention, various changes and modifications of the present invention are possible, these changes
Change and improvement all fall within the protetion scope of the claimed invention.The claimed scope of the invention by appended claims and its
Equivalent thereof.
Claims (5)
1. a kind of resistant to sea water corrodes the non-burning brick preparation method of acidproof slag micropowder and clay, it is characterised in that:By slag micropowder
It is placed in mixed liquor, stirs, 300 DEG C of thermophilic digestion mixed liquors, 1 as a child, filtering, takes out slag micropowder, mixes and stir with clay
Mix, the water for adding 50% deal continues stirring and obtains compound;
Compound is obtained into adobe through vibration moulding, Superfine slag powder baking-free brick is obtained after the maintenance of adobe normal temperature;
Comprise the following steps that:
Modified epoxy is taken to add in reactor, stirring is warming up to 85 DEG C, acrylic acid, epoxychloropropane is then added dropwise and to benzene
The mixed liquor of diphenol, stirring reaction 4-5 hours, obtain preformed objects A;
Take talcum powder to add in reactor, be heated to 130 DEG C when stirring vacuumizes and be incubated 1h;80 DEG C are subsequently cooled to, to
Titanium dioxide is added dropwise in reactor to be incubated while stirring, 90 DEG C are progressively warming up to after being added dropwise and is incubated 2 hours, is cooled down out
Material, obtains preformed objects B;
Preformed objects A and preformed objects B are put into distilling apparatus, carry out vacuum exhaust using vavuum pump so that the vacuum of distilling apparatus
Degree reaches about 0.6-1Pa, opens heater and heats heater block and condensing part respectively so that the temperature of heater block is protected
Hold at 550-600 DEG C, the temperature of condensing part is maintained at 320-340 DEG C, continuous vacuum distillation 5-6 hours;
After vacuum distillation terminates, distillate is collected, adds curing agent, silane coupler, stirs 5~6 minutes, then adds quartz
Sand and liquid low-molecular polyamide, stir 20~22 minutes, add organosilicon acrylic resin emulsion, stir 9~10 minutes, finally add
Enter thickener, be stirred for 10~12 minutes, be then filled into bucket, precipitate, collect upper liquid, obtain mixed liquor;
Mica powder, silica flour, carborundum powder, titanium dioxide zirconium powder and mild-clay powder are added sequentially to stir 3-5 in mixer
Minute, it is well mixed, obtains mixed powder;
Solid after precipitation is collected, mixed with mixed powder, the mud added after impurity elimination, is stirred continuously, adds the water of 1 times of amount
Point, heated, at a temperature of 300 DEG C, after heating 2 minutes, add adhesive for polyurethane, stir 3-5 minutes, it is well mixed to obtain
Clay,
Slag micropowder is placed in mixed liquor, stirred, 300 DEG C of thermophilic digestion mixed liquors, 1 as a child, filtering, it is micro- to take out slag
Powder, mixed with clay, the water for adding 50% deal continues stirring and obtains compound;The ratio of slag micropowder and clay is
9:1;
Compound is obtained into adobe through vibration moulding, Superfine slag powder baking-free brick is obtained after the maintenance of adobe normal temperature.
2. the non-burning brick preparation method of acidproof slag micropowder and clay is corroded according to a kind of resistant to sea water described in claim 1,
It is characterized in that:Each component content is respectively in above-mentioned steps:Modified epoxy 10-12 parts, acrylic acid 2-6 parts, epoxy chlorine
Propane 12-15 parts, hydroquinones 5-9 parts, talcum powder 5-8 parts, titanium dioxide 2-6 parts, curing agent 10-11 parts, silane coupler
5-6 parts, quartz sand 20-26 parts, liquid low-molecular polyamide 16-19 parts, organosilicon acrylic resin emulsion 20-30 parts, thickener 2-5
Part, mica powder 10-15 parts, silica flour 10-15 parts, carborundum powder 10-15 parts, titanium dioxide zirconium powder and mild-clay powder 10-15 parts,
Mud 5000-6000 parts, adhesive for polyurethane 50-60 parts.
3. the non-burning brick preparation method of acidproof slag micropowder and clay is corroded according to a kind of resistant to sea water described in claim 1,
It is characterized in that:Described adhesive for polyurethane is prepared including following components:
Ethylene glycol 30-35 parts, adipic acid 75-80 parts, ethyl acetate 5-20 parts, toluene di-isocyanate(TDI) 25-30 parts, butyl acetate
20-25 parts, trimethylolpropane 5-7 parts, polyester 5-7 parts.
4. the non-burning brick preparation method of acidproof slag micropowder and clay is corroded according to a kind of resistant to sea water described in claim 3,
It is characterized in that:Described adhesive for polyurethane, which comprises the following steps, to be prepared:
The preparation of polyadipate-ethylene glycol includes
1. ethylene glycol is put into reactor, heating stirring, while adipic acid is added, progressively heat up, be warming up in 2 hours
200℃;
2. when acid number reaches 35mgKOH/g, Depressor response kettle, 0.05Mpa, water outlet 8 hours are decompressed to;
3. when acid number reaches 15mgKOH/g, Depressor response kettle, 0.5Mpa is decompressed to, is discharged when controlling acid number 2mgKOH/g.
The preparation of modified poly ester includes
1. putting into 5 parts of butyl acetates in reactor, half an hour is stirred, polyester is added, is heated to 60 DEG C, adds 5 parts of toluene
Diisocyanate;
2. being warming up to 100-120 DEG C, ethyl acetate, mixed dissolution are added.
The preparation of modified isocyanate includes
1. adding remaining toluene di-isocyanate(TDI) and remaining butyl acetate in a kettle, stir;
2. add trimethylolpropane;
3. being heated to 70 DEG C, heat 1 hour;
4. it is cooled to room temperature.
After the completion of preparation, modified poly ester and modified isocyanate are mixed, proportion 100:20-50, add polyadipate-second two
Alcohol, 190 DEG C are warming up to, heating duration 1 hour, is condensed into 50-60 parts, you can obtain the adhesive for polyurethane of high bonding strength.
5. the non-burning brick preparation method of acidproof slag micropowder and clay is corroded according to a kind of resistant to sea water described in claim 1,
It is characterized in that:Described part is parts by weight.
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Cited By (1)
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CN108863282A (en) * | 2018-07-18 | 2018-11-23 | 合肥择浚电气设备有限公司 | It is a kind of to utilize the non-burning brick and preparation method thereof of food factory's rubbish preparation |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103043977A (en) * | 2012-12-14 | 2013-04-17 | 昆明钢铁控股有限公司 | Superfine slag powder baking-free brick and production method thereof |
CN104073212A (en) * | 2014-06-25 | 2014-10-01 | 安徽神舟飞船胶业有限公司 | Formula and preparation process of polyurethane adhesive with high adhesion strength |
CN105885759A (en) * | 2016-04-07 | 2016-08-24 | 主义 | Epoxy resin polymer daub and preparation method thereof |
-
2017
- 2017-09-05 CN CN201710792112.9A patent/CN107500609A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103043977A (en) * | 2012-12-14 | 2013-04-17 | 昆明钢铁控股有限公司 | Superfine slag powder baking-free brick and production method thereof |
CN104073212A (en) * | 2014-06-25 | 2014-10-01 | 安徽神舟飞船胶业有限公司 | Formula and preparation process of polyurethane adhesive with high adhesion strength |
CN105885759A (en) * | 2016-04-07 | 2016-08-24 | 主义 | Epoxy resin polymer daub and preparation method thereof |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108863282A (en) * | 2018-07-18 | 2018-11-23 | 合肥择浚电气设备有限公司 | It is a kind of to utilize the non-burning brick and preparation method thereof of food factory's rubbish preparation |
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