CN110451921A - A kind of polymeric phosphoric acid magnesium class composite material with heat insulating effect - Google Patents

A kind of polymeric phosphoric acid magnesium class composite material with heat insulating effect Download PDF

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CN110451921A
CN110451921A CN201910813457.7A CN201910813457A CN110451921A CN 110451921 A CN110451921 A CN 110451921A CN 201910813457 A CN201910813457 A CN 201910813457A CN 110451921 A CN110451921 A CN 110451921A
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phosphoric acid
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emulsifier
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陈金长
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    • 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
    • C04B24/00Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/40Compounds containing silicon, titanium or zirconium or other organo-metallic compounds; Organo-clays; Organo-inorganic complexes
    • C04B24/42Organo-silicon compounds
    • C04B24/425Organo-modified inorganic compounds, e.g. organo-clays
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    • 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
    • C04B28/34Compositions 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 cold phosphate binders
    • C04B28/344Compositions 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 cold phosphate binders the phosphate binder being present in the starting composition solely as one or more phosphates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F212/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02Monomers containing only one unsaturated aliphatic radical
    • C08F212/04Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/06Hydrocarbons
    • C08F212/08Styrene
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F236/00Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F236/02Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F236/04Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
    • C08F236/10Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated with vinyl-aromatic monomers
    • 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
    • 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
    • C04B2111/28Fire resistance, i.e. materials resistant to accidental fires or high temperatures
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    • 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
    • C04B2201/30Mortars, concrete or artificial stone characterised by specific physical values for heat transfer properties such as thermal insulation values, e.g. R-values
    • C04B2201/32Mortars, concrete or artificial stone characterised by specific physical values for heat transfer properties such as thermal insulation values, e.g. R-values for the thermal conductivity, e.g. K-factors
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
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  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
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  • Structural Engineering (AREA)
  • Dispersion Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
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Abstract

The present invention is a kind of polymeric phosphoric acid magnesium class composite material with heat insulating effect, the following steps are included: water, (methyl) styrene, butadiene, vinyl monomer, carboxylic monomer, silane coupling agent and emulsifier A are added in reaction kettle, material in kettle is mixed, is uniformly dispersed;After mixing, temperature is increased, initiator is added;After reaction, add magnesium phosphate and magnesium silicate, obtain material A;Calcium oxide, sepiolite, emulsifier B is added in water, material A in blender, obtains impregnating material A;In blender plus water, immersion expect A, gypsum, bentonite, magnesia, magnesia, Tourmaline mountain flour, closed pore glass bead, aluminium dihydrogen phosphate, stirring.Carboxy polymer and inorganic material are carried out good combination by silane coupling agent by the present invention, solve the problems, such as that heat insulation effect existing for traditional inorganic composite materials is poor, interior wall blade coating rear surface smoothness is low.One layer of fine and close, smooth protective film is formed on interior wall scraping coating surface by polymer, good heat insulation effect can be played.

Description

A kind of polymeric phosphoric acid magnesium class composite material with heat insulating effect
Technical field
The present invention relates to the polymeric phosphoric acid magnesium class composite materials of field of compound material more particularly to a kind of insulation Preparation method.
Background technique
In recent years, due to improvement of living standard, requirement of the people for quality of life is higher and higher, is especially embodied in room In terms of the finishing in room, more and more composite materials enter the ranks of coating for wall surface.And these composite materials belong to mostly In inorganic material, due to the characteristic of inorganic material itself, there are biggish difference for the size and uniformity of particle.And not It is mixed and is glued with merely by simple mechanical mixture between inorganic material and by the way of a variety of adhesives Knot.Since the size distribution of each inorganic material is inconsistent, the uniformity coefficient of partial size is also different, this results in the coating produced In coating surface of wall, the smooth surface in a surface cannot be formed.Just at last by increasing the substances such as some adhesives, There are still certain protrusions and recess on surface.Moreover, the addition of adhesive can destroy to a certain extent it is subtle between material Hole, so that its heat insulating effect declines.
Summary of the invention
It is an object of the invention to solve above-mentioned technical problem, propose that a kind of polymeric phosphoric acid magnesium class of insulation is compound The preparation method of material.
A kind of preparation method of the polymeric phosphoric acid magnesium class composite material of insulation of the present invention, including with the following group Point and its weight fraction:
(methyl) styrene: 1-10;
Butadiene: 1-5;
Vinyl monomer: 0.1-1;
Carboxylic monomer: 0.1-0.5;
Emulsifier A:0.05-0.1;
Emulsifier B:1-10;
Initiator: 0.01-0.05;
Silane coupling agent: 0.1-0.5;
Magnesium phosphate: 10-20;
Closed pore glass bead: 10-15;
Calcium oxide: 1-5;
Magnesium silicate: 5-10;
Magnesia: 1-10;
Bentonite: 1-10;
Sepiolite: 10-20;
Magnesia: 0.1-1;
Tourmaline mountain flour: 1-3;
Aluminium dihydrogen phosphate: 1-10;
Water: 100-200.
A kind of preparation method of the polymeric phosphoric acid magnesium class composite material of insulation of the present invention, including following step It is rapid:
S1, suitable water, (methyl) styrene, butadiene, vinyl monomer, carboxyl list are added in the reaction kettle of certain capacity Body, silane coupling agent and emulsifier A open stirring and mix material in kettle, are uniformly dispersed;
S2, after mixing increases temperature of reaction kettle to 80-90 DEG C, initiator initiated polymerization is then added;
S3, reaction continue 3-5h at 85-95 DEG C;After reaction, reaction temperature is reduced to 60-70 DEG C, and phosphorus is then added Sour magnesium and magnesium silicate, insulation reaction 1--3h;
S4, after reaction reduces reaction temperature to room temperature, obtains material A;
S5, the water that 40% is added in blender, blender revolving speed are promoted to 40-60 revs/min per minute, are gradually added into object Expect A, adds calcium oxide, sepiolite in stirring;Emulsifier B is added in stirring 5-after ten minutes, continues 15-30 minutes materials of stirring It after material is uniform, is put into fermentation vat and impregnates 10-12 hours, obtain impregnating material A;
S6, suitable quantity of water is added in blender, blender revolving speed is adjusted to 40-60 revs/min, and the above-mentioned institute prepared is added There is immersion material A, to be mixed 5-after ten minutes, adds gypsum, bentonite, magnesia, magnesia, Tourmaline mountain flour, stirring 10-30 minutes;
S7,60-80 revs/min of blender speed is promoted, closed pore glass bead is added, adds biphosphate after mixing evenly Aluminium finally stirs 15-30 minutes.
Further, the vinyl monomer in acrylamide, acrylonitrile, N- hydroxyl first acrylamide at least one Kind.
Further, the carboxylic monomer is selected from least one of acrylic acid, fumaric acid, itaconic acid.
Further, the emulsifier A and emulsifier B is selected from neopelex, lauryl sodium sulfate, discrimination Change at least one of rosin acid potash soap.
Further, the silane coupling agent is selected from 3- triethoxysilyl -1- propylamine, γ-Methacrylamide At least one of oxygroup propyl trimethoxy silicane, phenylaminomethyl triethoxysilane.
Butylbenzene class latex is a kind of high molecular polymer.Since its own partial size is smaller (90nm -140nm), using lotion The particle diameter distribution for the polymer beads that the mode of polymerization obtains is also relatively uniform.Silane is added during synthesis in the present invention Coupling agent, the siloxy on silane coupling agent have preferable reactivity for inorganic matter, the organic moiety in structure There is preferable compatibility for organic matter.It therefore, can be with when silane coupling agent is between organic layer and inorganic layer Form organic layer-silane coupling agent-inorganic layer binder course, inorganic material and organic material can be carried out merging well and Connection.In the present invention, first by together with the monomer polymerization reactions such as silane coupling agent and butadiene, styrene, then it will need again The inorganic raw material magnesium phosphate and magnesium silicate being attached are added in reaction system, are acted on silane coupling agent, will be organic Layer with inorganic layer is good is combined together.
Meanwhile on the one hand the addition of emulsifier participates in emulsion polymerization, be conducive to generate that partial size is smaller and uniform cream Micelle;On the other hand, after the addition of some inorganic raw materials, original emulsion system can be broken, and emulsion particle is demulsified, in The organic matter containing siloxy is combined with inorganic matter and gradually disperses under the action of stirring on the strand of portion's package. And emulsifier can be present in system with free state, system is played reduce surface tension, increase the lubrication of storeroom with And provide certain plastication.
Polymer after demulsification is agitated, action of soaking can be very good to be dispersed between inorganic material, these dispersions Polymer in composite material in use, due to composite inner moisture evaporation, the water molecule layer between polymer constantly subtracts Few, the strong intermolecular force (such as intermolecular hydrogen bonding) between polymer can promote polymer molecule to link together, A firm polymer network is formed, wherein by inorganic material package, plays the role of adhesive.
In addition, composite material use when, in outermost polymer can it is agglomerated together formation one layer it is smooth , fine and close, transparent polymer film, play waterproof, moisture resistance and the effect of heat preservation.
Specific embodiment
The present invention is described in more detail below by specific embodiment, for a better understanding of of the present invention Specific embodiments of the present invention are described in detail below, but it is merely an example, the present invention is not restricted to following The specific embodiment of description.To those skilled in the art, the equivalent modifications and substitute also all that any couple of present invention carries out Among scope of the invention.Therefore, made equal transformation and modification without departing from the spirit and scope of the invention, is all answered Cover within the scope of the invention.
Embodiment 1:
30 kilograms of water, 1 kilogram of styrene, 1 kilogram of butadiene, 0.1 are added in the reaction kettle with stirring and heating function Kilogram acrylamide, 0.1 kilogram of acrylic acid, 0.1 kilogram of 3- triethoxysilyl -1- propylamine and 0.05 kilogram of dodecane Base benzene sulfonic acid sodium salt.Stirring is then turned on to mix material in kettle, be uniformly dispersed;After mixing, temperature of reaction kettle is increased to 80 DEG C, 0.01 kilogram of potassium peroxydisulfate initiator initiated polymerization is then added;Reaction continues 5h at 85 DEG C.Reaction terminates Afterwards, reaction temperature is reduced to 60 DEG C, and 10 kilograms of magnesium phosphate and 5 kilograms of magnesium silicate, insulation reaction 3h is then added.Reaction knot Shu Hou reduces reaction temperature to room temperature, obtains material A.Then 40 kilograms of water is added in blender, blender revolving speed is promoted To 40 revs/min per minute, it is gradually added into material A.After addition, add under stirring conditions 1 kilogram of calcium oxide, 10 kilograms of sepiolites.Stirring after ten minutes be added 1 kilogram of neopelex, continue stir 30 minutes materials it is uniform after, It is put into fermentation vat to impregnate 12 hours, obtains impregnating material A.Be added 30 kg of water in blender, blender revolving speed adjust to 40 turns/ Minute, be added above-mentioned all immersion material A prepared, it is to be mixed after ten minutes, add 1 kilogram of bentonite, 1 kilogram of water chestnut hardship Soil, 0.1 kilogram of magnesia and 1 kilogram of Tourmaline mountain flour stir 30 minutes.60 revs/min of blender speed are then lifted out, is added 10 kilograms of closed pore glass beads add 1 kg of phosphoric acid aluminum dihydrogen after mixing evenly, finally stir 30 minutes.
Embodiment 2:
50 kilograms of water, 5 kilograms of styrene, 3 kilograms of butadiene, 0.5 are added in the reaction kettle with stirring and heating function Kilogram acrylonitrile, 0.3 kilogram of fumaric acid, 0.3 kilogram of γ-methacryl azyloxy propyl trimethoxy silicane and 0.08 are public The lauryl sodium sulfate of jin.Stirring is then turned on to mix material in kettle, be uniformly dispersed;After mixing, reaction kettle is increased Then 0.03 kilogram of sodium peroxydisulfate initiator initiated polymerization is added to 85 DEG C in temperature;Reaction continues 4h at 90 DEG C.Instead After answering, reaction temperature is reduced to 65 DEG C, 15 kilograms of magnesium phosphate and 8 kilograms of magnesium silicate, insulation reaction 2h is then added. After reaction, reaction temperature is reduced to room temperature, obtains material A.Then 60 kilograms of water is added in blender, blender turns Speed is promoted to 50 revs/min per minute, is gradually added into material A.After addition, 3 kilograms are added under stirring conditions Calcium oxide, 15 kilograms of sepiolites.5 kilograms of lauryl sodium sulfate are added after stirring 8 minutes, it is uniform to continue 20 minutes materials of stirring Afterwards, it is put into fermentation vat to impregnate 11 hours, obtains impregnating material A.40 kg of water are added in blender, blender revolving speed is adjusted to 50 Rev/min, the above-mentioned all immersion material A prepared are added, after 8 minutes to be mixed, add 5 kilograms of bentonites, 5 kilograms of water chestnut hardships Soil, 0.5 kilogram of magnesia and 2 kilograms of Tourmaline mountain flours stir 30 minutes.70 revs/min of blender speed are then lifted out, is added 13 kilograms of closed pore glass beads add 5 kg of phosphoric acid aluminum dihydrogens after mixing evenly, finally stir 20 minutes.
Embodiment 3:
60 kilograms of water, 10 kilograms of methyl styrenes, 5 kilograms of fourths two are added in the reaction kettle with stirring and heating function Alkene, 1 kilogram of N hydroxymethyl acrylamide, 0.5 kilogram of itaconic acid, 0.5 kilogram of phenylaminomethyl triethoxysilane and 0.1 are public The isproportionated potassium rosinate of jin.Stirring is then turned on to mix material in kettle, be uniformly dispersed;After mixing, reaction kettle is increased Then 0.05 kilogram of ammonium persulfate initiator initiated polymerization is added to 90 DEG C in temperature;Reaction continues 3h at 95 DEG C.Instead After answering, reaction temperature is reduced to 70 DEG C, 20 kilograms of magnesium phosphate and 10 kilograms of magnesium silicate, insulation reaction is then added 1h.After reaction, reaction temperature is reduced to room temperature, obtains material A.Then 80 kilograms of water, stirring are added in blender Machine revolving speed is promoted to 60 revs/min per minute, is gradually added into material A.After addition, 5 are added under stirring conditions Kilogram calcium oxide, 20 kilograms of sepiolites.10 kilograms of isproportionated potassium rosinates are added in stirring after five minutes, continue to stir 15 minutes materials It after material is uniform, is put into fermentation vat and impregnates 10 hours, obtain impregnating material A.60 kg of water, blender revolving speed tune are added in blender Whole to 60 revs/min, be added above-mentioned all immersion material A prepared, it is to be mixed after five minutes, add 10 kilograms of bentonites, 10 Kilogram magnesia, 1 kilogram of magnesia and 3 kilograms of Tourmaline mountain flours stir 10 minutes.It is then lifted out 80 revs/min of blender speed 15 kilograms of closed pore glass beads are added in clock, add 10 kg of phosphoric acid aluminum dihydrogens after mixing evenly, finally stir 15 minutes i.e. It can.
Comparative example 1:
The insulating mold coating referring to made from patent CN106398405B.
Comparative example 2:
The insulating mold coating referring to made from patent CN108467645A.
Above-described embodiment 1-3 and the obtained insulating mold coating of comparative example 1-2 are subjected to performance comparison, as a result such as Table 1:
Table
Wherein, the measurement of (1) thermal coefficient: certain thickness plate is made in above-mentioned different materials, concrete mode is referring to GB/ The measurement of T10294-2008 standard testing progress thermal coefficient.
(2) measurement of surface strength: being made certain thickness plate for above-mentioned different materials, with surface strength analyzer into The detection of row surface strength.
(3) measurement of surface flatness: above-mentioned different materials are uniformly applied on cardboard, smearing thickness 2cm, with other Gram formula smoothness instrument is detected.
Pass through the comparison of above-mentioned data form 1, it can be seen that a kind of polymeric phosphoric acid of insulation provided by the invention The preparation method of the preparation method of magnesium class composite material, is superior to pair in thermal coefficient, surface strength and surface smoothness Ratio.
Beneficial effects of the present invention: the present invention is carried out Carboxy polymer and inorganic material by silane coupling agent good Combination, solve the problems, such as that heat insulation effect existing for traditional inorganic composite materials is poor, interior wall blade coating rear surface smoothness is low. It is by the effect of crosslinked polymer network, inorganic material is fixed wherein, bonding inorganic powder is played instead of traditional adhesive The effect of material.One layer of fine and close, smooth protective film is formed on interior wall scraping coating surface by polymer again, can be played good Heat insulation effect is scratched using composite material prepared by the present invention in interior wall simultaneously because polymer film has stronger hydrophobicity There is good waterproof effect afterwards.

Claims (7)

1. a kind of preparation method of the polymeric phosphoric acid magnesium class composite material of insulation, which is characterized in that including following components And its weight fraction:
(methyl) styrene: 1-10;
Butadiene: 1-5;
Vinyl monomer: 0.1-1;
Carboxylic monomer: 0.1-0.5;
Emulsifier A:0.05-0.1;
Emulsifier B:1-10;
Initiator: 0.01-0.05;
Silane coupling agent: 0.1-0.5;
Magnesium phosphate: 10-20;
Closed pore glass bead: 10-15;
Calcium oxide: 1-5;
Magnesium silicate: 5-10;
Magnesia: 1-10;
Bentonite: 1-10;
Sepiolite: 10-20;
Magnesia: 0.1-1;
Tourmaline mountain flour: 1-3;
Aluminium dihydrogen phosphate: 1-10;
Water: 100-200.
2. a kind of preparation method of the polymeric phosphoric acid magnesium class composite material of insulation of the present invention, which is characterized in that The following steps are included:
S1, suitable water, (methyl) styrene, butadiene, vinyl monomer, carboxyl list are added in the reaction kettle of certain capacity Body, silane coupling agent and emulsifier A open stirring and mix material in kettle, are uniformly dispersed;
S2, after mixing increases temperature of reaction kettle to 80-90 DEG C, initiator initiated polymerization is then added;
S3, reaction continue 3-5h at 85-95 DEG C;After reaction, reaction temperature is reduced to 60-70 DEG C, and phosphorus is then added Sour magnesium and magnesium silicate, insulation reaction 1--3h;
S4, after reaction reduces reaction temperature to room temperature, obtains material A;
S5, the water that 40% is added in blender, blender revolving speed are promoted to 40-60 revs/min per minute, are gradually added into object Expect A, adds calcium oxide, sepiolite in stirring;Emulsifier B is added in stirring 5-after ten minutes, continues 15-30 minutes materials of stirring It after material is uniform, is put into fermentation vat and impregnates 10-12 hours, obtain impregnating material A;
S6, suitable quantity of water is added in blender, blender revolving speed is adjusted to 40-60 revs/min, and the above-mentioned institute prepared is added There is immersion material A, to be mixed 5-after ten minutes, adds gypsum, bentonite, magnesia, magnesia, Tourmaline mountain flour, stirring 10-30 minutes;
S7,60-80 revs/min of blender speed is promoted, closed pore glass bead is added, adds biphosphate after mixing evenly Aluminium finally stirs 15-30 minutes.
3. the preparation method of the polymeric phosphoric acid magnesium class composite material of a kind of insulation according to claim 1, feature It is, the vinyl monomer is selected from least one of acrylamide, acrylonitrile, N- hydroxyl first acrylamide.
4. the preparation method of the polymeric phosphoric acid magnesium class composite material of a kind of insulation according to claim 1, feature It is, the carboxylic monomer is selected from least one of acrylic acid, fumaric acid, itaconic acid.
5. the preparation method of the polymeric phosphoric acid magnesium class composite material of a kind of insulation according to claim 1, feature It is, the emulsifier A and emulsifier B are selected from neopelex, lauryl sodium sulfate, isproportionated potassium rosinate At least one of.
6. the preparation method of the polymeric phosphoric acid magnesium class composite material of a kind of insulation according to claim 1, feature It is, the silane coupling agent selects 3- triethoxysilyl -1- propylamine, γ-methacryl azyloxy propyl trimethoxy At least one of base silane, phenylaminomethyl triethoxysilane.
7. the preparation method of the polymeric phosphoric acid magnesium class composite material of a kind of insulation according to claim 1, feature It is, the initiator is selected from least one of sodium peroxydisulfate, ammonium persulfate, potassium peroxydisulfate.
CN201910813457.7A 2019-08-30 2019-08-30 A kind of polymeric phosphoric acid magnesium class composite material with heat insulating effect Pending CN110451921A (en)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101658893B1 (en) * 2015-08-26 2016-09-23 범준이엔씨 주식회사 Modified sulfur binder composition, method for preparing modified sulfur binder, modified sulfur binder using the same and modified asphalt composition comprising the same
CN106830873A (en) * 2017-02-17 2017-06-13 于斌 Multi-functional composite magnesium silicate heat preserving and insulating material formula and preparation technology
CN109438621A (en) * 2018-11-09 2019-03-08 新辉(中国)新材料有限公司 Functional butylbenzene copolymer latex and its preparation method and application
CN109456030A (en) * 2018-12-11 2019-03-12 陈金长 A kind of composite magnesium silicate building roof heat preserving and insulating material formula and preparation process
CN109592960A (en) * 2018-12-17 2019-04-09 利宙实业(泗阳)有限公司 A kind of composite magnesium silicate soaking material and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101658893B1 (en) * 2015-08-26 2016-09-23 범준이엔씨 주식회사 Modified sulfur binder composition, method for preparing modified sulfur binder, modified sulfur binder using the same and modified asphalt composition comprising the same
CN106830873A (en) * 2017-02-17 2017-06-13 于斌 Multi-functional composite magnesium silicate heat preserving and insulating material formula and preparation technology
CN109438621A (en) * 2018-11-09 2019-03-08 新辉(中国)新材料有限公司 Functional butylbenzene copolymer latex and its preparation method and application
CN109456030A (en) * 2018-12-11 2019-03-12 陈金长 A kind of composite magnesium silicate building roof heat preserving and insulating material formula and preparation process
CN109592960A (en) * 2018-12-17 2019-04-09 利宙实业(泗阳)有限公司 A kind of composite magnesium silicate soaking material and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
毛致林,王宽城: "《电力技经人员实用手册》", 31 March 2000, 中国电力出版社 *

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Application publication date: 20191115