CN105670455A - Solvent-free epoxy anti-permeability barrier coating and method for preparing same - Google Patents

Solvent-free epoxy anti-permeability barrier coating and method for preparing same Download PDF

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Publication number
CN105670455A
CN105670455A CN201610038887.2A CN201610038887A CN105670455A CN 105670455 A CN105670455 A CN 105670455A CN 201610038887 A CN201610038887 A CN 201610038887A CN 105670455 A CN105670455 A CN 105670455A
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curing agent
amine curing
component
glycidyl ether
phenol
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王浩
师力
曾照坤
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Beijing Tianshan New Material Technology Co Ltd
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Beijing Tianshan New Material Technology Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D163/00Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/50Amines
    • C08G59/56Amines together with other curing agents
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/62Alcohols or phenols
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/63Additives non-macromolecular organic
    • EFIXED CONSTRUCTIONS
    • E01CONSTRUCTION OF ROADS, RAILWAYS, OR BRIDGES
    • E01CCONSTRUCTION OF, OR SURFACES FOR, ROADS, SPORTS GROUNDS, OR THE LIKE; MACHINES OR AUXILIARY TOOLS FOR CONSTRUCTION OR REPAIR
    • E01C7/00Coherent pavings made in situ
    • E01C7/08Coherent pavings made in situ made of road-metal and binders
    • E01C7/35Toppings or surface dressings; Methods of mixing, impregnating, or spreading them
    • E01C7/356Toppings or surface dressings; Methods of mixing, impregnating, or spreading them with exclusively synthetic resin as a binder; Aggregate, fillers or other additives for application on or in the surface of toppings having exclusively synthetic resin as binder
    • EFIXED CONSTRUCTIONS
    • E01CONSTRUCTION OF ROADS, RAILWAYS, OR BRIDGES
    • E01DCONSTRUCTION OF BRIDGES, ELEVATED ROADWAYS OR VIADUCTS; ASSEMBLY OF BRIDGES
    • E01D19/00Structural or constructional details of bridges
    • E01D19/08Damp-proof or other insulating layers; Drainage arrangements or devices ; Bridge deck surfacings
    • E01D19/083Waterproofing of bridge decks; Other insulations for bridges, e.g. thermal ; Bridge deck surfacings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Architecture (AREA)
  • Civil Engineering (AREA)
  • Structural Engineering (AREA)
  • Epoxy Resins (AREA)
  • Sealing Material Composition (AREA)

Abstract

The invention relates to a solvent-free epoxy anti-permeability barrier coating.The solvent-free epoxy anti-permeability barrier coating comprises components A and components B.The components A comprise, by weight, 80-100 parts of epoxy resin, 5-15 parts of flexibility improving resin, 5-15 parts of diluents, 0-1 part of defoaming agents and 0.1-0.5 part of leveling agents; the components B comprise, by weight, 80-100 parts of modified amine curing agents and 0-5 parts of silane coupling agents.The solvent-free epoxy anti-permeability barrier coating is mainly used for waterproof treatment on cement base planes and has the advantages of low viscosity, high elongation, adhesion and toughness and the like.

Description

A kind of no-solvent type impervious seal coat of ring oxygen and its preparation method
Technical field
The present invention relates to adhesive industry, particularly relate to a kind of no-solvent type impervious seal coat of ring oxygen and its preparation method.
Background technology
In the fast development building especially road and bridge, high ferro industry in industry, higher requirement is proposed in base face, due to the easy water-absorbent of cement, often due to moisture in cement matrix and cause the reduction in the work-ing life to whole road surface. In order to prevent the corrosion problem that moisture in cement causes and then the work-ing life improving overall road surface, bridge floor, it is imperative that road surface, bridge floor carry out the WATER REPELLENT in cement based face. The water-proof materials such as current cement based face water-proof system many employings modified bituminous pitch coiled material, polyurea system. The paving of modified bituminous pitch coiled material is covered to be needed to be processed in base face, simultaneously also not high with the adhesiveproperties of cement; If cement based face or matrix exist water molecules, can occur with polyurea system to react the risk simultaneously having small molecules release and produce bubble, the film-forming properties on surface and the work-ing life of overall road surface and bridge floor can be affected. Especially now to the raising of environmental requirement, a lot of occasion does not re-use solvent type adhesive, the no-solvent type Epoxy waterproof system that the present invention relates to has low viscosity, snappiness, the cementability high with cement based face, easy to operate, there will be no and the risk problem of water molecule reaction in cement, and also have relatively excellent adhesion property with cement based face when certain wet surface construction.
CN103849296A discloses a kind of elastic epoxy resin waterproof paint and its preparation method, wherein adopt epoxy resin and the conventional modified amine curing agent main raw material as A, B component, and add the flexibility that softening agent improves material, but the elasticity of this waterproof paint, toughness and cohesiveness still have much room for improvement.
Summary of the invention
It is an object of the invention to for the deficiencies in the prior art, it is provided that a kind of no-solvent type impervious seal coat of ring oxygen, this coating has the features such as low viscosity, snappiness, high tenacity, high adhesion and ease for operation, it is possible to be applicable to the WATER REPELLENT in cement based face.
In order to realize the object of the present invention, it is proposed to following technical scheme:
A kind of no-solvent type impervious seal coat of ring oxygen, with weight parts, component A consists of:
B component consists of:
Modified amine curing agent 80~100 parts
Silane coupling agent 0~5 part;
Component A mixes with the ratio of weight ratio 10:1 to 1:10 with B component, it is preferable that weight ratio 1:1.
Described modified amine curing agent is prepared from by polyetheramine, N-aminoethyl piperazine, amine curing agent, phenol and paracril. It is preferably multi-ethylene polyamines, it is more preferable to be triethylene tetramine, tetraethylene pentamine, diethylenetriamine.
Described amine curing agent is phenolic aldehyde amine curing agent, one or more in polyamide curing agent, fat cyclammonium solidifying agent and fatty amine curing agent;
Described phenol is alkylphenol, it is preferable to nonyl phenol.
Described polyetheramine, N-aminoethyl piperazine, amine curing agent, phenol and paracril proportioning by weight is 8-10:5-7:0.5-1.5:8-10:3-7.
Described epoxy resin is one or more mixtures in bisphenol A epoxide resin, bisphenol F epoxy resin, novolac epoxy, hydrogenated bisphenol A epoxy resin;
The soft resin of described increasing is longer chain polyethylene glycols glycidyl ether liquid resin, long-chain polypropylene glycol glycidyl ether liquid resin and/or long-chain polytetramethylene glycol glycidyl ether liquid resin;
Described thinner is response type epoxide diluent, it is preferable to the mixture of one or more in alkyl glycidyl ether, butylglycidyl ether, phenyl glycidyl ether, benzyl glycidyl ether, ethylene glycol diglycidylether, propylene glycol diglycidylether, butyleneglycol glycidyl ether.
Described defoamer is the broken bubble polymers soln not containing organosilicon.
Described flow agent is polyether-modified polydimethylsiloxane interpolymer.
The preparation method of described modified amine curing agent is: join in flask by polyetheramine, N-aminoethyl piperazine, amine curing agent, phenol, and logical nitrogen protection, at 40 DEG C of insulated and stirred 2~3h; raised temperature to 60 DEG C again; add paracril, insulated and stirred 3-5h, it is cooled to room temperature for subsequent use.
In described B component, silane coupling agent is KH-550 coupling agent.
Present invention also offers the preparation method of the above-mentioned no-solvent type impervious seal coat of ring oxygen, comprise the steps:
1) modified amine curing agent is prepared:
In proportion polyetheramine, N-aminoethyl piperazine, amine curing agent, phenol are joined in flask, logical nitrogen protection, at 40 DEG C of insulated and stirred 2~3h, then raised temperature to 60 DEG C, add paracril, insulated and stirred 3-5h, it is cooled to room temperature for subsequent use; Wherein polyetheramine, N-aminoethyl piperazine, amine curing agent, phenol and paracril proportioning by weight is 8-10:5-7:0.5-1.5:8-10:3-7;
2) component A is prepared:
(1) described epoxy resin, increase soft resin preheating 6-8h at 60 DEG C of temperature in advance;
(2) adding epoxy resin in normal temperature situation first in proportion, increase soft resin, thinner, defoamer, flow agent in Scattered Kettle, high-speed stirring 20~30min, maintenance vacuum tightness is-0.095~-0.100MPa;
(3) clearing up stirrer gear and still wall, continue stirring at low speed 10~15min, maintenance vacuum tightness is-0.040~-0.050MPa, then discharging packing;
3) B component is prepared:
(1) first proportionally adding modified amine curing agent, silane coupling agent at room temperature and stir 20~30min in Scattered Kettle, maintenance vacuum tightness is-0.095~-0.100MPa;
(2) clearing up stirrer gear and still wall, continue stirring 5~6min, maintenance vacuum tightness is-0.095~-0.100MPa, then discharging packing.
Present invention also offers the application of the above-mentioned impervious seal coat of ring oxygen in the WATER REPELLENT of cement based face.
The advantage of the present invention and effect are system not containing solvent, adopt modified amine curing agent prepared by certain party method, it is possible to effective the carrying out promoting curing reaction, improve the mechanical property of epoxy resin;The impervious seal coat prepared has low viscosity, snappiness, the advantage of the cementability high with cement based face, easy to operate, there will be no and the risk problem of water molecule reaction in cement, and also have relatively excellent adhesion property with cement based face when certain wet surface construction.
Embodiment
For making the object, technical solutions and advantages of the present invention clearly understand, and in conjunction with specific embodiments, the technical scheme of the present invention is further described;
Embodiment 1
1) modified amine curing agent is prepared:
Polyetheramine, N-aminoethyl piperazine, triethylene tetramine, nonyl phenol are joined in flask, logical nitrogen protection, at 40 DEG C of insulated and stirred 2h, then raised temperature to 60 DEG C, add paracril, insulated and stirred 3h, it is cooled to room temperature for subsequent use; Wherein polyetheramine, N-aminoethyl piperazine, triethylene tetramine, nonyl phenol and paracril proportioning by weight is 8.5:5.6:0.5:9:4;
2) component A is prepared:
(1) described bisphenol A epoxide resin, double F epoxy resin and longer chain polyethylene glycols glycidyl ether liquid resin preheating 6-8h at 60 DEG C of temperature in advance;
(2) in normal temperature situation, bisphenol A epoxide resin 60 parts, double F epoxy resin 30 parts, longer chain polyethylene glycols glycidyl ether liquid resin 10 parts, alkyl glycidyl ether 10 parts, defoamer 0.2 part, polyether-modified polydimethylsiloxane interpolymer 0.1 part are joined in Scattered Kettle, high-speed stirring 25min, maintenance vacuum tightness is-0.095~-0.100MPa;
(3) clearing up stirrer gear and still wall, continue stirring at low speed 12min, maintenance vacuum tightness is-0.040~-0.050MPa, then discharging packing;
3) B component is prepared:
(1) add modified amine curing agent 100 parts at room temperature, KH-550 coupling agent 2 parts in Scattered Kettle, stir 20min, maintenance vacuum tightness is-0.095~-0.100MPa;
(2) clearing up stirrer gear and still wall, continue to stir 5min, maintenance vacuum tightness is-0.095~-0.100MPa, then discharging packing.
During use, component A is that 8:3 mixes with B component according to weight ratio.
Embodiment 2
1) modified amine curing agent is prepared:
Polyetheramine, N-aminoethyl piperazine, tetraethylene pentamine, nonyl phenol are joined in flask, logical nitrogen protection, at 40 DEG C of insulated and stirred 2.5h, then raised temperature to 60 DEG C, add paracril, insulated and stirred 3h, it is cooled to room temperature for subsequent use; Wherein polyetheramine, N-aminoethyl piperazine, tetraethylene pentamine, nonyl phenol and paracril proportioning by weight is 9:5:1:8:6;
2) component A is prepared:
(1) described novolac epoxy, long-chain polypropylene glycol glycidyl ether liquid resin preheating 7h at 60 DEG C of temperature in advance;
(2) in normal temperature situation, novolac epoxy 85 parts, long-chain polypropylene glycol glycidyl ether liquid resin 6 parts, ethylene glycol diglycidylether 10 parts, defoamer 0.2 part, polyether-modified polydimethylsiloxane interpolymer 0.1 part are joined in Scattered Kettle, high-speed stirring 25min, maintenance vacuum tightness is-0.095~-0.100MPa;
(3) clearing up stirrer gear and still wall, continue stirring at low speed 12min, maintenance vacuum tightness is-0.040~-0.050MPa, then discharging packing;
3) B component is prepared:
(1) add modified amine curing agent 95 parts at room temperature, KH-550 coupling agent 4 parts in Scattered Kettle, stir 20min, maintenance vacuum tightness is-0.095~-0.100MPa;
(2) clearing up stirrer gear and still wall, continue to stir 5min, maintenance vacuum tightness is-0.095~-0.100MPa, then discharging packing.
During use, component A is that 1:1.5 mixes with B component according to weight ratio.
Embodiment 3
1) modified amine curing agent is prepared:
In proportion polyetheramine, N-aminoethyl piperazine, diethylenetriamine, nonyl phenol are joined in flask, logical nitrogen protection, at 40 DEG C of insulated and stirred 2~3h, then raised temperature to 60 DEG C, add paracril, insulated and stirred 3-5h, it is cooled to room temperature for subsequent use; Wherein polyetheramine, N-aminoethyl piperazine, diethylenetriamine, nonyl phenol and paracril proportioning by weight is 9.6:5.3:1.5:10:6;
2) component A is prepared:
(1) described hydrogenated bisphenol A epoxy resin, bisphenol F epoxy resin and long-chain polytetramethylene glycol glycidyl ether liquid resin preheating 6-8h at 60 DEG C of temperature in advance;
(2) in normal temperature situation, add hydrogenated bisphenol A epoxy resin 50 parts, bisphenol F epoxy resin 40 parts first in proportion, long-chain polytetramethylene glycol glycidyl ether liquid resin 10 parts, butyleneglycol glycidyl ether 10 parts, defoamer 0.2 part, polyether-modified polydimethylsiloxane interpolymer 0.1 part are in Scattered Kettle, high-speed stirring 30min, maintenance vacuum tightness is-0.095~-0.100MPa;
(3) clearing up stirrer gear and still wall, continue stirring at low speed 14min, maintenance vacuum tightness is-0.040~-0.050MPa, then discharging packing;
3) B component is prepared:
(1) first proportionally add modified amine curing agent 100 parts at room temperature, KH-550 coupling agent 3 parts in Scattered Kettle, stir 28min, maintenance vacuum tightness is-0.095~-0.100MPa;
(2) clearing up stirrer gear and still wall, continue to stir 6min, maintenance vacuum tightness is-0.095~-0.100MPa, then discharging packing.
During use, component A is that 1:1 mixes with B component according to weight ratio.
In above-described embodiment, evenly rear injection corresponding mould sample preparation to be mixed.
Comparative example
By the bisphenol F epoxy resin of 65 weight parts, the butylglycidyl ether of 8 weight parts, 1 weight part wetting agent (HX-4020), 1 weight part defoamer (BYK-052 is without organosilicon broken bubble polymers soln), 1 weight part flow agent (polyester modification polydimethylsiloxane solution), 2 parts by weight of plasticizer (acrylate), white cement is crossed 200 order sieves and is got 30 weight parts, 15 parts sulfuric acid barium, 15 weight part 325 order silica powders, the heavy calcium of 15 weight part 600 orders, 300 weight part 80-120 order quartz sands mix and obtain component A,
The anilinomethyl triethoxysilane of the butylglycidyl ether modified amine curing agent of 20 weight parts, 2 weight parts, 2 weight part trolamines are mixed and obtain B component;
Component A thing and B component are mixed in proportion, injects corresponding mould sample preparation.
As shown in the table with its performance of product test of embodiment 1~3 and comparative example:
0 viscosity: according to GB/T1723-1993 standard testing gained;
1 surface drying time: according to GB/T16777-2008 standard testing gained;
2 do solid work the time: according to GB/T16777-2008 standard testing gained;
3 with cementitious intensity: according to JC/T975-2005 standard testing gained;
4 tensile strengths: according to GB/T528-2009 standard testing gained;
5 elongation at breaks: according to GB/T528-2009 standard testing gained;
6 shore hardnesses: according to GB/T531.1-2008 standard testing gained.
As can be seen from the table, the exercise elongation of embodiment is higher than normal level >=82% of epoxy glue, also higher level >=5.4MPa is maintained with the bonding strength of cement, and maintain lower viscosity≤88s, compared with existing elastic epoxy resin waterproof paint, tensile strength and elongation at break all have and significantly improve.
The above embodiment only have expressed embodiments of the present invention, and it describes comparatively concrete and detailed, but therefore can not be interpreted as the restriction to patent scope of the present invention. , it is also possible to make some distortion and improvement, it should be appreciated that for the person of ordinary skill of the art, without departing from the inventive concept of the premise these all belong to protection scope of the present invention. Therefore, the protection domain of patent of the present invention should be as the criterion with claims.

Claims (8)

1. the impervious seal coat of no-solvent type ring oxygen, comprises component A and B component, it is characterised in that, with weight parts, component A consists of:
B component consists of:
Modified amine curing agent 80~100 parts
Silane coupling agent 0~5 part;
Described modified amine curing agent is prepared from by polyetheramine, N-aminoethyl piperazine, amine curing agent, phenol and paracril;
Component A mixes with the ratio of weight ratio 10:1 to 1:10 with B component, it is preferable that weight ratio is 1:1.
2. the impervious seal coat of ring oxygen according to claim 1, it is characterised in that, described amine curing agent is phenolic aldehyde amine curing agent, one or more in polyamide curing agent, fat cyclammonium solidifying agent and fatty amine curing agent;
Described phenol is alkylphenol, it is preferable to nonyl phenol.
3. the impervious seal coat of ring oxygen according to claim 2, it is characterised in that, described amine curing agent is multi-ethylene polyamines, it is preferable to triethylene tetramine, tetraethylene pentamine, diethylenetriamine.
4. the impervious seal coat of ring oxygen according to claim 1, it is characterised in that, described polyetheramine, N-aminoethyl piperazine, amine curing agent, phenol and paracril proportioning by weight is 8-10:5-7:0.5-1.5:8-10:3-7.
5. the impervious seal coat of ring oxygen according to claim 1; it is characterized in that; the preparation method of described modified amine curing agent is: join in flask by polyetheramine, N-aminoethyl piperazine, amine curing agent, phenol; logical nitrogen protection; at 40 DEG C of insulated and stirred 2~3h, then raised temperature to 60 DEG C, add paracril; insulated and stirred 3-5h, is cooled to room temperature for subsequent use.
6. the impervious seal coat of ring oxygen according to claim 1, it is characterised in that, described epoxy resin is the mixture of one or more in bisphenol A epoxide resin, bisphenol F epoxy resin, novolac epoxy, hydrogenated bisphenol A epoxy resin;
The soft resin of described increasing is longer chain polyethylene glycols glycidyl ether liquid resin, long-chain polypropylene glycol glycidyl ether liquid resin and/or long-chain polytetramethylene glycol glycidyl ether liquid resin;
Described thinner is response type epoxide diluent, it is preferable to one or more mixtures in alkyl glycidyl ether, butylglycidyl ether, phenyl glycidyl ether, benzyl glycidyl ether, ethylene glycol diglycidylether, propylene glycol diglycidylether, butyleneglycol glycidyl ether;
Described defoamer is the broken bubble polymers soln not containing organosilicon;
Described flow agent is polyether-modified polydimethylsiloxane interpolymer;
Described silane coupling agent is KH-550 coupling agent.
7. the preparation method of the impervious seal coat of ring oxygen according to any one of claim 1-6, it is characterised in that, comprise the steps:
1) modified amine curing agent is prepared:
Polyetheramine, N-aminoethyl piperazine, amine curing agent, phenol are joined in flask, logical nitrogen protection, at 40 DEG C of insulated and stirred 2~3h, then raised temperature to 60 DEG C, add paracril, insulated and stirred 3-5h, it is cooled to room temperature for subsequent use;Wherein polyetheramine, N-aminoethyl piperazine, amine curing agent, phenol and paracril proportioning by weight is 8-10:5-7:0.5-1.5:8-10:3-7;
2) component A is prepared:
(1) described epoxy resin, increase soft resin preheating 6-8h at 60 DEG C of temperature in advance;
(2) adding epoxy resin in normal temperature situation first in proportion, increase soft resin, thinner, defoamer, flow agent in Scattered Kettle, high-speed stirring 20~30min, maintenance vacuum tightness is-0.095~-0.100MPa;
(3) clearing up stirrer gear and still wall, continue stirring at low speed 10~15min, maintenance vacuum tightness is-0.040~-0.050MPa, then discharging packing;
3) B component is prepared:
(1) first proportionally adding modified amine curing agent, silane coupling agent at room temperature and stir 20~30min in Scattered Kettle, maintenance vacuum tightness is-0.095~-0.100MPa;
(2) clearing up stirrer gear and still wall, continue stirring 5~6min, maintenance vacuum tightness is-0.095~-0.100MPa, then discharging packing.
8. application in the WATER REPELLENT of cement based face of the impervious seal coat of ring oxygen described in the arbitrary item of claim 1-6.
CN201610038887.2A 2016-01-20 2016-01-20 Solvent-free epoxy anti-permeability barrier coating and method for preparing same Pending CN105670455A (en)

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CN108059859A (en) * 2018-01-23 2018-05-22 合肥峰腾节能科技有限公司 A kind of novel anti-crack roofing spray film water-proofing material
CN109054387A (en) * 2017-12-19 2018-12-21 广州市犀力化工有限公司 Compound polysiloxanes of a kind of no-solvent type Thief zone reaction and preparation method thereof
CN109096877A (en) * 2018-09-07 2018-12-28 广州尚卓新材料科技有限公司 A kind of epoxy composite and preparation method thereof that can be improved concrete surface intensity and waterproof performance and can be used in wet surface
CN111622458A (en) * 2020-05-25 2020-09-04 杨华 Anti-fouling water-based terrace and construction method thereof
CN113372535A (en) * 2021-05-31 2021-09-10 张家港衡业特种树脂有限公司 Preparation method and use method of modified epoxy resin curing agent
CN115321043A (en) * 2021-09-10 2022-11-11 中石化石油工程技术服务有限公司 Method for separately collecting and temporarily storing hazardous wastes for field oil-gas exploration
CN115637094A (en) * 2022-10-24 2023-01-24 中昊北方涂料工业研究设计院有限公司 Protective coating system for cast magnesium alloy and preparation and use methods thereof

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CN106366842A (en) * 2016-08-26 2017-02-01 安徽建邦建材有限公司 High-elasticity epoxy coating for thermal insulating wall
CN106905816A (en) * 2017-03-06 2017-06-30 华东理工大学 Super-hydrophobic oleophobic coating and preparation method thereof and application method
CN107793817B (en) * 2017-09-18 2020-07-14 苏州吉人高新材料股份有限公司 Organic-inorganic composite fluorescent montmorillonite-doped fluorescent paint and preparation method thereof
CN107793817A (en) * 2017-09-18 2018-03-13 苏州吉人高新材料股份有限公司 A kind of organo-mineral complexing fluorescence that adulterates covers fluorescent paint of support soil and preparation method thereof
CN109054387A (en) * 2017-12-19 2018-12-21 广州市犀力化工有限公司 Compound polysiloxanes of a kind of no-solvent type Thief zone reaction and preparation method thereof
CN108059859A (en) * 2018-01-23 2018-05-22 合肥峰腾节能科技有限公司 A kind of novel anti-crack roofing spray film water-proofing material
CN109096877A (en) * 2018-09-07 2018-12-28 广州尚卓新材料科技有限公司 A kind of epoxy composite and preparation method thereof that can be improved concrete surface intensity and waterproof performance and can be used in wet surface
CN111622458A (en) * 2020-05-25 2020-09-04 杨华 Anti-fouling water-based terrace and construction method thereof
CN111622458B (en) * 2020-05-25 2021-07-20 杨华 Anti-fouling water-based terrace and construction method thereof
CN113372535A (en) * 2021-05-31 2021-09-10 张家港衡业特种树脂有限公司 Preparation method and use method of modified epoxy resin curing agent
CN115321043A (en) * 2021-09-10 2022-11-11 中石化石油工程技术服务有限公司 Method for separately collecting and temporarily storing hazardous wastes for field oil-gas exploration
CN115637094A (en) * 2022-10-24 2023-01-24 中昊北方涂料工业研究设计院有限公司 Protective coating system for cast magnesium alloy and preparation and use methods thereof
CN115637094B (en) * 2022-10-24 2023-11-10 中昊北方涂料工业研究设计院有限公司 Cast magnesium alloy protective coating system and preparation and use methods thereof

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