CN105949987B - A kind of imine modified polyaspartic ester water proof anti-corrosive paint and preparation method and application - Google Patents

A kind of imine modified polyaspartic ester water proof anti-corrosive paint and preparation method and application Download PDF

Info

Publication number
CN105949987B
CN105949987B CN201610547533.0A CN201610547533A CN105949987B CN 105949987 B CN105949987 B CN 105949987B CN 201610547533 A CN201610547533 A CN 201610547533A CN 105949987 B CN105949987 B CN 105949987B
Authority
CN
China
Prior art keywords
component
polyaspartic ester
water proof
proof anti
corrosive paint
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN201610547533.0A
Other languages
Chinese (zh)
Other versions
CN105949987A (en
Inventor
张维欣
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangdong Reach Engineering Technology Co Ltd
Original Assignee
Guangdong Reach Engineering Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Guangdong Reach Engineering Technology Co Ltd filed Critical Guangdong Reach Engineering Technology Co Ltd
Priority to CN201610547533.0A priority Critical patent/CN105949987B/en
Publication of CN105949987A publication Critical patent/CN105949987A/en
Application granted granted Critical
Publication of CN105949987B publication Critical patent/CN105949987B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/08Polyurethanes from polyethers
    • 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/08Anti-corrosive paints
    • 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
    • C09D7/61Additives non-macromolecular inorganic
    • 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
    • C09D7/65Additives macromolecular
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

The invention discloses a kind of imine modified polyaspartic ester water proof anti-corrosive paint and preparation method and applications.The coating includes first component and component B:The composition of first component is as follows:Polyaspartic ester 46~61%, imines 38.5~53.5% and accelerating agent 0.1%~0.5%;The composition of second component is as follows:Isocyanate functional group's component 50~61%, low viscosity epoxy compound 11~15%, nano fumed silica 5~8%, filler 18~27%, pigment 1% and other auxiliary agents 2%.By the ingredient mixing in first component to get first component;By the ingredient mixing in second component to get second component;In use, by first component and second component in mass ratio 1:3~1:4.5 are uniformly mixed, you can are coated on sheet metal or concrete construction surface.Coating water-proof performance provided by the present invention is good, and adhesive property is strong, is solventless coatings.

Description

A kind of imine modified polyaspartic ester water proof anti-corrosive paint and preparation method with Using
Technical field
The present invention relates to a kind of coating, more particularly to a kind of imine modified polyaspartic ester water proof anti-corrosive paint and system Preparation Method and application.
Background technology
Concrete becomes modern infrastructure and civil buildings, sea because of its excellent robustness, durability and safety etc. The essential construction material such as harbor work's journey, road, bridge, tunnel.However, for a long time by the physics of ambient enviroment, chemistry, biology Effect is so that concrete volume expansion just occurs successively after the completion of concrete works after a period of time, cracking even destroys etc. Defect drastically influences safety and the service life of concrete construction engineering.
Water is the main cause and carrier for causing concrete destruction.Moisture can lead to direct physical change such as frost and defrosting and The tension of generation, water are also the carrier for transmitting corrosive substance such as chlorion, sour gas, poisonous substance etc..Therefore, as long as being avoided that Concrete is in direct contact with moisture, so that it may to effectively improve concrete durability.
At present applied to concrete construction engineering water proof anti-corrosive paint mainly have modified epoxy resin mortar, polyurethane coating, Vinyl resin paint, organosilicon alkanes, acrylate paint and carbamide paint.Polyaspartic Ester-Based Coatings are to exist in recent years It is poly- to revolutionize tradition for a kind of novel aliphatic, long response time and the high performance two-component coating that polyurea industry field occurs The shortcomings of gel time of urea coating is short and easy xanthochromia.Compared with conventional urethane coating, and with solid content height, hardness and coagulate The advantages that glue time is adjustable, good corrosion resistance, thick can apply, excellent in abrasion resistance.
However, 103031045 A of patent CN1880393A, CN103788857B, CN discloses the poly- day of bi-component at present L-aminobutanedioic acid ester polyureas elastic waterproof anti-corrosive paint, isocyanate component are divided into A, B component with polyaspartic ester group.But this Or a little formulation for coating material occur can rapid draings but validity period is short or validity period often but the defect of slow-drying.In order to regulate and control Reactivity, as patent CN1880393A, CN102391771A, CN103865370B disclose the blocked amine using low viscosity, Such as ketimide and aldimine are used in mixed way with polyaspartic ester.But the imidization used in these current patents Conjunction object content is relatively low, and effect is only limitted to the curing activity of regulation and control coating.In actual repair concrete construction engineering process, Contain more Free water in the surface of concrete construction defect, crack, it is difficult to by it during water proof anti-corrosive paint penetrates into Discharge, causes Polyaspartic Ester-Based Coatings after hardening and the combination on concrete construction surface is poor, be susceptible to coating Layer and concrete cracking, especially highway, subway tunnel and high-speed railway crack apparent after being given a shock.
It is suitable for repairing the coating of concrete construction therefore, it is necessary to continue research and development.
Invention content
The primary purpose of the present invention is that the shortcomings that overcoming the prior art and deficiency, provide a kind of imine modified poly- lucid asparagus Propylhomoserin ester water proof anti-corrosive paint.
Another object of the present invention is to provide the preparations of the imine modified polyaspartic ester water proof anti-corrosive paint Method.
It is still another object of the present invention to provide the applications of the imine modified polyaspartic ester water proof anti-corrosive paint.
The purpose of the invention is achieved by the following technical solution:A kind of imine modified polyaspartic ester waterproof and anticorrosion painting Material, including first component and component B:
First component by as follows by mass percentage at being grouped as:Polyaspartic ester 46~61%, imines 38.5 ~53.5% and accelerating agent 0.1%~0.5%;
Second component by as follows by mass percentage at being grouped as:It is isocyanate functional group's component 50~61%, low viscous Spend epoxide 11~15%, nano fumed silica 5~8%, filler 18~27%, pigment 1% and other auxiliary agents 2%.
Quality proportioning when the first component and the second component use is:First component:Second component=1:3~1: 4.5。
The polyaspartic ester is that dicarboxylic esters reacts the Michael additions generated production with primary amine through catalysis Object, addition compound product contains secondary amine, and anti-life reacts to form cured product with isocyanates.Polyaspartic ester includes that laboratory is logical Cross the addition compound product and other commercially available polyaspartic esters that dicarboxylic esters is prepared with primary amine reaction, preferably Bayer One kind or at least two in F-420, F-524, F-520 and F220 is flown upward in Desmophen NH1420, NH1520, NH1220, Zhuhai Kind.
The imines is reacted according to Mannich to be prepared:By polyamine and sealer in molar ratio 1:2 proportioning mixing, then The catalyst of catalytic amount is added, warming while stirring is warming up to 90~120 DEG C, is stirred to react 3~5 hours;It is subsequently added into band water Agent, shunting remove the moisture generated in reaction system, until the quality of water entrainer band water outlet reaches theoretical value;Continue to be warming up to phase It answers near the boiling point of sealer, vacuum distillation removes the sealer for not participating in reaction in water entrainer and system, obtains imines (such as formula Shown in I);Its reaction process is shown below:
The imines is more preferably prepared by following specific steps:By 1 mole of polyamine and 2 moles of closing Agent is added in the reaction kettle with division box, and 0.2~0.3 gram of catalyst is added, is while stirring raised to the temperature of system 90~120 DEG C;After stirring 3~5 hours, 100~120mL water entrainers are added, shunt the moisture generated in removing system, until The quality of water entrainer band water outlet reaches theoretical value.Continue to be warming up near the boiling point of corresponding sealer, vacuum distillation removes band water The sealer for not participating in reaction in agent and system, obtains imines.
The polyamine can be the low molecular weight amine compound containing two or more than two molecule of primary amine, preferably Diethylenetriamine, triethylene tetramine, tetraethylenepentamine, hexamethylene diamine, isophorone diamine, 4,4 '-diamino-dicyclohexyl methanes At least one of with 3,3 '-dimethyl -4,4 '-diamino-dicyclohexyl methane.
The sealer can be containing carbonyl and the organic compound that can be reacted with the anti-raw Mannich of primary amine, it is excellent It is selected as at least one of ketone or aldehyde.
The ketone is preferably that acetone, acetophenone, cyclohexanone, cyclopentanone, bicyclo-propyl ketone, cyclopentylethanone and methyl are different One kind in butyl ketone or at least two.
The aldehyde is preferably propionic aldehyde, butyraldehyde, aldehyde C-9, hexanal, n-octaldehyde, valeral, furtural, capraldehyde, pyroracemic aldehyde, benzene Formaldehyde, the hendecanal, phenylacetaldehyde, the third formaldehyde of ring, phenyl-allylene aldehyde, thiophenecarboxaldehyde, benzaldehyde iodine, 2- pyridine carboxaldehydes and 5- indolecarboxaldehydes Middle one kind or at least two.
The water entrainer is preferably one or both of hexamethylene and toluene.
The content of the accelerating agent is preferably mass percent 0.5%.
The accelerating agent is dibutyl tin laurate, stannous octoate and one kind in isooctyl acid bismuth or at least two.
Isocyanate functional group's component is main ingredient in second component, is and imines, polyaspartic ester The co-curing ingredient for forming solidfied material, in order to balance the mobility of coating and to the cladding function of coating, isocyanate-functional The number-average molecular weight of group's component can be 1000~15000 grams/mol, preferably 2000~8000 grams/mol;It is diisocyanate The modifier of ester and polyether polyol, the modifier are mainly prepared by the following method:Polyether polyol is added to reaction kettle Interior, heat temperature raising, stirring vacuumizes, and temperature is 110~120 DEG C inside, vacuum degree 133.3Pa is dehydrated 2~3h;Then 50 are cooled to DEG C, it is added dropwise and diisocyanate cpd is added, the addition of diisocyanate cpd presses the OH groups of polyether polyol:Two is different NCO group=molar ratio 1 of cyanate esters:1.4~1:2.3 calculating;Continue stirring after dripping 1~2 hour, addition is urged Agent is gradually warming up to 60~80 DEG C, constant temperature 3.5~6h of clock reaction, and cooling down, vacuumizing and defoaming obtains diisocyanate The modifier of ester and polyether polyol.
The polyether polyol is the polyalcohol that molecular weight is not higher than 2000 grams/mol, preferably polyether polyol N- 204, N-210, N-220, PTMEG (polytetramethylene ether glycol) -250, PTMEG-650, two functional group such as PTMEG-1000 One or both of polyether polyol.
The diisocyanate cpd is toluene di-isocyanate(TDI), methyl diphenylene diisocyanate, six Asias 1,6- Methyl diisocyanate, two isocyanide of isophorone diisocyanate, benzene dimethylene diisocyanate and cyclohexanedimethyleterephthalate One kind in acid esters or at least two.
The time of the stirring is preferably 2h.
The low viscosity epoxy compound refer to not hydroxyl, contain only the compound of epoxy group, preferably glycolylurea ring One kind in oxygen resin, ethylene glycol diglycidylether and 1,4-butanediol diglycidyl ether or at least two, more preferably Glycolylurea epoxide resin.
The filler is preferably titanium dioxide, silicon powder, flyash, talcum powder, sericite in powder, blanc fixe, heavy One kind in calcium carbonate and precipitated calcium carbonate or at least two.
The pigment is preferably carbon black.
Other described auxiliary agents are that molecular formula is HO- [Si (CH3)2-O]n- H and the low molecular weight hydroxyl of polymerization degree n=6~11 Dimethyl silicone polymer, gamma-aminopropyl-triethoxy-silane or the N- phenylaminomethyl triethoxysilanes of base sealing end.
The preparation method of the imine modified polyaspartic ester water proof anti-corrosive paint, includes the following steps:
(1) polyaspartic ester, imines and accelerating agent are uniformly mixed, obtain first component;Wherein, each component presses quality Percentages are as follows:Polyaspartic ester 46~61%, imines 38.5~53.5% and accelerating agent 0.1%~0.5%;
(2) by isocyanate functional group's component, low viscosity epoxy compound, nano fumed silica, filler, pigment and Other auxiliary agents are uniformly mixed, and obtain second component;Wherein, each component is as follows by mass percentage:Isocyanate functional group's component 50~61%, low viscosity epoxy compound 11~15%, nano fumed silica 5~8%, filler 18~27%, pigment 1% With other auxiliary agents 2%.
The application of the imine modified polyaspartic ester water proof anti-corrosive paint, includes the following steps:By first component With component B in mass ratio 1:3~1:4.5 are uniformly mixed, and are coated on sheet metal or concrete construction surface.
The concrete construction is the concrete construction of humidity.
The thickness for the film that the coating is formed is preferably 1.5~2mm.
The present invention has the following advantages and effects with respect to the prior art:
(1) present invention increases the content of group with imine moiety, and not only group with imine moiety can regulate and control curing activity, moreover it is possible to it is mixed The Free water on solidifying soil surface reacts, and reduces influence of the Free water to water proof anti-corrosive paint and the deterioration of concrete adhesive force, together When, the carbonyl containing compound generated is reacted with water can play the role of levelling agent, enhance the apparent property of water proof anti-corrosive paint, disappear Removing coating pin hole further increases its waterproof effect.
(2) present invention introduces a part of low viscosity epoxy compounds and polyurethane to form B component, is handed over altogether by curing reaction It is linked in paint solidification object, further improves the bonding force of coating and concrete surface, realize the raising of coating durability.
(3) viscosity of group with imine moiety and low viscosity epoxy compound itself is very low in the present invention, can effectively improve painting The mobility of material realizes solventless coatings, reduces the wasting of resources and environmental pollution caused by organic matter volatilization, and to construction The damage of personnel.
(4) group with imine moiety replaces part polyaspartic ester to participate in reaction in the present invention, when the gel of formulation for coating material Between adjustable extent it is wider, construction flexibility enhancing.
Specific implementation mode
With reference to embodiment, the present invention is described in further detail, and embodiments of the present invention are not limited thereto.
Embodiment 1
(1) synthesis of aldimine
Equipped with blender, water knockout drum, condenser pipe there-necked flask in be added 103 grams of diethylenetriamine, be slowly added dropwise into benzene 0.3 gram of 723 cation exchange resin of catalyst is added in 212 grams of formaldehyde, and warming while stirring is reacted 3 hours to 90 DEG C.It is added The temperature of reaction system is increased to 115 by cyclohexane 100mL when the quality of separated water is close to 36 grams of theoretical value DEG C, it boils off and has neither part nor lot in reaction dissolvent, obtain diphenyl imine (as shown in Formula II) and its closed is stored in dry brown bottle It is interior.
(2) preparation of first component
Polyaspartic ester DesmophenNH1420,49.5wt% structural formula that 50wt% Bayers are produced is Formula II Diphenyl imine and the isooctyl acid bismuth of 0.5wt% be uniformly mixed at normal temperatures, stand 6 hours, obtain first component.
(3) preparation of second component
Polyether polyol N-204 is added in reaction kettle, heat temperature raising, stirring vacuumizes.Temperature is 110 DEG C, very inside Reciprocal of duty cycle 133.3Pa is dehydrated 2h.It is cooled to 50 DEG C;It is 1 by the molar ratio of OH and NCO:2.1 are added dropwise addition toluene di-isocyanate(TDI), Continue stirring 2 hours after dripping, catalyst dibutyltin dilaurylate is added, is gradually warming up to 60 DEG C, constant temperature clock reaction 3.5h, cooling down, vacuumizing and defoaming obtain diisocyanate and polyether polyols that molecular weight is 3000~4000 grams/mol The modifier of alcohol.By the aforementioned modified objects of 58wt%, 12wt% glycolylurea epoxide resins (Wuxi Meihua Chemical Co., Ltd., MHRO70), 6wt% nano fumed silicas (wacker chemicals (China) Co., Ltd, N70, similarly hereinafter), 21wt% talcum powder (specialty minerals Co., Ltd of the U.S., AG609, similarly hereinafter), 1wt% carbon blacks (Columbian Chemical, Raven 1255, similarly hereinafter) and The dimethyl silicone polymer (DOW CORNING 107) of 2wt% low-molecular-weight hydroxyls sealing end is uniformly mixed by high-speed dispersion system, is obtained Component B.
(4) preparation of water proof anti-corrosive paint
According to first component:Second component=1:4.5 stir evenly after be coated in metallic plate and moist cement concrete (humidity Cement concrete is that " 8 " type matrix after dry solidification is complete impregnates acquisition in 7 days in pure water, similarly hereinafter) surface, film thickness control In 1.5~2.0mm.Its testing result is as shown in table 1.
Embodiment 2
(1) synthesis of aldimine
Equipped with blender, water knockout drum, condenser pipe there-necked flask in be added 146 grams of triethylene tetramine, be slowly added dropwise into benzene 0.3 gram of 723 cation exchange resin is added in 212 grams of formaldehyde, and warming while stirring is reacted 3 hours to 90 DEG C.Hexamethylene is added The temperature of reaction system is increased to 115 DEG C, boiled off by water entrainer 100mL when the quality of separated water is close to 36 grams of theoretical value Reaction dissolvent is had neither part nor lot in, diphenyl imine (as shown in formula III) is obtained and closed is stored in its in dry brown bottle.
(2) preparation of first component
Polyaspartic ester DesmophenNH1520,53.5wt% structural formula that 46wt% Bayers are generated is formula III Diphenyl imine and the isooctyl acid bismuth of 0.5wt% be uniformly mixed at normal temperatures, stand 6 hours.
(3) preparation of second component
Polyether polyol N-204 is added in reaction kettle, heat temperature raising, stirring vacuumizes.Temperature is 110 DEG C, very inside Reciprocal of duty cycle 133.3Pa is dehydrated 2h.It is cooled to 50 DEG C;It is 1 by the molar ratio of OH and NCO:2.3 are added dropwise addition isophorone diisocyanate Ester continues stirring 2 hours after dripping, catalyst dibutyltin dilaurylate is added, is gradually warming up to 60 DEG C, constant temperature timing is anti- Answer 4h, cooling down, vacuumizing and defoaming, obtain isophorone diisocyanate that molecular weight is 3000~4000 grams/mol with The modifier of polyether polyol.By the aforementioned modified objects of 61wt%, 13wt% ethylene glycol diglycidylethers (expand abundant chemical industry in Changshu City Co., Ltd, HHY669), 5wt% nano fumed silicas, 18wt% talcum powder, 1wt% carbon blacks and 2wt% low molecular weights Hydroxy-end capped dimethyl silicone polymer is uniformly mixed by high-speed dispersion system.
(4) preparation of water proof anti-corrosive paint
According to first component:Second component=1:3.4 stir evenly after be coated in metallic plate and moist cement concrete surface, film Thickness control is in 1.5~2.0mm.The results are shown in Table 1 for it.
Embodiment 3
(1) synthesis of ketimide
Equipped with blender, water knockout drum, condenser pipe there-necked flask in be added 146 grams of triethylene tetramine, be slowly added dropwise into ring 0.2 gram of FeCl is added in 196 grams of hexanone3, warming while stirring is to 100 DEG C, reaction 5 hours.Water entrainer toluene 120mL is added, waits for When the quality of separated water is close to 36 grams of theoretical value, the temperature of reaction system is increased to 125 DEG C, boils off that have neither part nor lot in reaction molten Agent obtains diphenyl imine (as shown in formula IV) and closed is stored in its in dry brown bottle.
(2) preparation of first component
Polyaspartic ester DesmophenNH1520,38.5wt% structural formula that 61wt% Bayers are generated is formula IV Diphenyl imine and the dibutyl tin laurate of 0.5wt% be uniformly mixed at normal temperatures, stand 6 hours.
(3) preparation of second component
Polyether polyol N-204 is added in reaction kettle, heat temperature raising, stirring vacuumizes.Temperature is 110 DEG C, very inside Reciprocal of duty cycle 133.3Pa is dehydrated 2h.It is cooled to 50 DEG C;It is 1 by the molar ratio of OH and NCO:1.4 are added dropwise addition isophorone diisocyanate Ester continues stirring 2 hours after dripping, catalyst dibutyltin dilaurylate is added, is gradually warming up to 80 DEG C, constant temperature timing is anti- Answer 6h, cooling down, vacuumizing and defoaming, obtain isophorone diisocyanate that molecular weight is 5000~8000 grams/mol with The modifier of polyether polyol.By the aforementioned modified objects of 51wt%, 15wt% glycolylurea epoxide resins, 8wt% nano-gas-phase titanium dioxides Silicon, 23wt% talcum powder, 1wt% carbon blacks and 2wt% gamma-aminopropyl-triethoxy-silanes (the military big organosilicon new material stock in Hubei Part Co., Ltd, WD-50, similarly hereinafter) be uniformly mixed by high-speed dispersion system.
(4) preparation of water proof anti-corrosive paint
According to first component:Second component=1:3 stir evenly after be coated in metallic plate and moist cement concrete surface, film thickness Degree control is in 1.5~2.0mm.The results are shown in Table 1 for it.
Embodiment 4
(1) synthesis of ketimide
Equipped with blender, water knockout drum, condenser pipe there-necked flask in be added 103 grams of diethylenetriamine, be slowly added dropwise into ring 0.2 gram of FeCl is added in 196 grams of hexanone3, warming while stirring is to 100 DEG C, reaction 5 hours.Cyclohexane 100mL is added, When the quality of separated water is close to 36 grams of theoretical value, the temperature of reaction system is increased to 115 DEG C, boils off that have neither part nor lot in reaction molten Agent obtains diphenyl imine (shown as a formula V) and closed is stored in its in dry brown bottle.
(2) preparation of first component
It is by polyaspartic ester F520,53.5wt% structural formula that 46wt% Zhuhai Feiyang Chemical Co., Ltd produces The diphenyl imine of Formula V and the dibutyl tin laurate of 0.5wt% are uniformly mixed at normal temperatures, stand 6 hours.
(3) preparation of second component
50wt% is modified addition product, 12wt% hydantoin epoxies according to isophorone diisocyanate prepared by embodiment 3 Resin, 8wt% nano fumed silicas, 27wt% talcum powder, 1wt% carbon blacks and 2wt% gamma-aminopropyl-triethoxy-silanes It is uniformly mixed by high-speed dispersion system.
(4) preparation of water proof anti-corrosive paint
According to first component:Second component=1:4 stir evenly after be coated in metallic plate and moist cement concrete surface, film thickness Degree control is in 1.5~2.0mm.The results are shown in Table 1 for it.
Embodiment 5
(1) synthesis of ketimide
Equipped with blender, water knockout drum, condenser pipe there-necked flask in be added 170 grams of isophorone diamine, be slowly added dropwise into 0.3 gram of SnCl is added in 210 grams of methyl iso-butyl ketone (MIBK)2, warming while stirring is to 90 DEG C, reaction 6 hours.Hexamethylene band water is added The temperature of reaction system is increased to 120 DEG C, boils off and do not join by agent 100mL when the quality of separated water is close to 36 grams of theoretical value Methyl iso-butyl ketone (MIBK) and reaction dissolvent, obtain diphenyl imine (as shown in Formula IV) and its closed be stored in dry brown In bottle.
(2) preparation of first component
It is by polyaspartic ester F220,41wt% structural formula that 58.5wt% Zhuhai Feiyang Chemical Co., Ltd produces The diphenyl imine of Formula IV and the dibutyl tin laurate of 0.5wt% are uniformly mixed at normal temperatures, stand 6 hours.
(3) preparation of second component
Polyether polyol PTMEG-250 is added in reaction kettle, heat temperature raising, stirring vacuumizes.Temperature is 120 inside DEG C, vacuum degree 133.3Pa be dehydrated 3h.It is cooled to 50 DEG C;It is 1 by the molar ratio of OH and NCO:1.6 are added dropwise addition six methylenes of 1,6- Group diisocyanate continues stirring 2 hours after dripping, catalyst dibutyltin dilaurylate is added, is gradually warming up to 65 DEG C, It is sub- to obtain 1, the 6- six that molecular weight is 3000~5000 grams/mol for constant temperature clock reaction 4h, cooling down, vacuumizing and defoaming Methyl diisocyanate is modified addition product.1, the 6- hexamethylene diisocyanates of 55wt% molecular weight are modified addition product, 11wt%1,4- butanediol diglycidyl ether, 6wt% nano fumed silicas, 25wt% talcum powder, 1wt% carbon blacks and 2wt%N- phenylaminomethyls triethoxysilane (Hangzhou Jesse blocks Chemical Co., Ltd., KH-ND42), passes through high speed dispersion system System is uniformly mixed.
(4) preparation of water proof anti-corrosive paint
According to first component:Second component=1:3 stir evenly after be coated in metallic plate and moist cement concrete surface, film thickness Degree control is in 1.5~2.0mm.The results are shown in Table 1 for it.
Comparative example 1
(1) preparation of first component
61wt% polyaspartic esters DesmophenNH1420, the 38.5wt% embodiment 3 that Bayer is generated prepares knot Structure formula is that the imines of IV and the isooctyl acid bismuth of 0.5wt% are uniformly mixed at normal temperatures, stands 6 hours.
(2) preparation of second component
The toluene di-isocyanate(TDI) that molecular weight prepared by 68wt% embodiments 1 is 3000~4000 grams/mol, which is modified, to be added At object, 6wt% nano fumed silicas, 23wt% talcum powder, 1wt% carbon blacks and 2wt% low-molecular-weight hydroxyls sealing end it is poly- Dimethyl siloxane is uniformly mixed by high-speed dispersion system.
(3) preparation of water proof anti-corrosive paint
According to first component:Second component=1:4.5 stir evenly after be coated in metallic plate and moist cement concrete surface, film Thickness control is in 1.5~2.0mm.The results are shown in Table 1 for it.
Comparative example 2
(1) preparation of first component
The isooctyl acid bismuth of 99.5wt% polyaspartic esters DesmophenNH1420,0.5wt% that Bayer generates are existed It is uniformly mixed under room temperature, stands 6 hours.
(2) preparation of second component
The toluene di-isocyanate(TDI) that molecular weight prepared by 57wt% embodiments 1 is 3000~4000 grams/mol, which is modified, to be added At object, 11wt% glycolylurea epoxide resins, 6wt% nano fumed silicas, 23wt% talcum powder, 1wt% carbon blacks and 2wt% are low The components such as the dimethyl silicone polymer of molecular weight hydroxy sealing end are uniformly mixed by high-speed dispersion system.
(3) preparation of water proof anti-corrosive paint
According to first component:Second component=1:4.5 stir evenly after be coated in metallic plate and moist cement concrete surface, film Thickness control is in 1.5~2.0mm.The results are shown in Table 1 for it.
Comparative example 3
(1) preparation of first component
Step in polyaspartic ester DesmophenNH1420,20wt% embodiment 1 that 79.5wt% Bayers are produced (1) the isooctyl acid bismuth of the diphenyl imine and 0.5wt% that synthesize is uniformly mixed at normal temperatures, is stood 6 hours, is obtained first component.
(2) preparation of second component
The toluene di-isocyanate(TDI) that 63wt% molecular weight is 3000~4000 grams/mol is modified addition product, 5wt% glycolylureas Epoxy resin, 6wt% nano fumed silicas, 23wt% talcum powder, 1wt% carbon blacks and 2wt% low-molecular-weight hydroxyls sealing end Dimethyl silicone polymer by high-speed dispersion system be uniformly mixed.
(3) preparation of water proof anti-corrosive paint
According to first component:Second component=1:4.5 stir evenly after be coated in metallic plate and moist cement concrete surface, film Thickness control is in 1.5~2.0mm.The results are shown in Table 1 for it.
As shown in Table 1, will more large content of imines and low viscosity epoxy compound collocation use, poly- day can be effectively improved The tensile strength of L-aminobutanedioic acid ester water proof anti-corrosive paint, impact resistance, heat aging property and to metal and moist cement The adhesive strength of concrete, while acid resistance in simple imine modified polyaspartic ester water proof anti-corrosive paint can be overcome bad Defect.
Product performance index prepared by table 1 is:
The above embodiment is a preferred embodiment of the present invention, but embodiments of the present invention are not by above-described embodiment Limitation, it is other it is any without departing from the spirit and principles of the present invention made by changes, modifications, substitutions, combinations, simplifications, Equivalent substitute mode is should be, is included within the scope of the present invention.

Claims (10)

1. a kind of imine modified polyaspartic ester water proof anti-corrosive paint, it is characterised in that including first component and component B:
First component by as follows by mass percentage at being grouped as:Polyaspartic ester 46~61%, imines 38.5~ 53.5% and accelerating agent 0.1%~0.5%;
Second component by as follows by mass percentage at being grouped as:Isocyanate functional group's component 50~61%, low viscosity ring Oxygen compound 11~15%, nano fumed silica 5~8%, filler 18~27%, pigment 1% and other auxiliary agents 2%.
2. imine modified polyaspartic ester water proof anti-corrosive paint according to claim 1, it is characterised in that:The first Quality proportioning when component and the second component use is:First component:Second component=1:3~1:4.5.
3. imine modified polyaspartic ester water proof anti-corrosive paint according to claim 1, it is characterised in that:
The imines is reacted according to Mannich to be prepared;
Isocyanate functional group's component is diisocyanate and the modifier of polyether polyol;
The low viscosity epoxy compound refer to not hydroxyl, contain only the compound of epoxy group;
Other described auxiliary agents are that molecular formula is HO- [Si (CH3)2-O]n- H and the low-molecular-weight hydroxyl of polymerization degree n=6~11 envelope Dimethyl silicone polymer, gamma-aminopropyl-triethoxy-silane or the N- phenylaminomethyl triethoxysilanes at end.
4. imine modified polyaspartic ester water proof anti-corrosive paint according to claim 3, it is characterised in that:
Isocyanate functional group's component is prepared by the following method:Polyether polyol is added in reaction kettle, is heated Heating, stirring vacuumize, and temperature is 110~120 DEG C inside, vacuum degree 133.3Pa is dehydrated 2~3h;Then 50 DEG C are cooled to, is added dropwise Diisocyanate cpd is added, the addition of diisocyanate cpd presses the OH groups of polyether polyol:Diisocyanate NCO group=molar ratio 1 of compound:1.4~1:2.3 calculating;Continue stirring after dripping 1~2 hour, catalyst be added, 60~80 DEG C, constant temperature 3.5~6h of clock reaction are gradually warming up to, cooling down, vacuumizing and defoaming obtains diisocyanate and gathers The modifier of ethoxylated polyhydric alcohol;
The preparation process of the imines is as follows:By polyamine and sealer in molar ratio 1:2 proportioning mixing, add catalytic amount Catalyst, warming while stirring is warming up to 90~120 DEG C, is stirred to react 3~5 hours;It is subsequently added into water entrainer, shunting removes The moisture generated in dereaction system, until the quality of water entrainer band water outlet reaches theoretical value;Continue to be warming up to corresponding sealer Boiling point near, vacuum distillation removes the sealer for not participating in reaction in water entrainer and system, obtains imines;
The low viscosity epoxy compound is that glycolylurea epoxide resin, ethylene glycol diglycidylether and 1,4- butanediols two shrink One kind in glycerin ether or at least two.
5. imine modified polyaspartic ester water proof anti-corrosive paint according to claim 4, it is characterised in that:
The polyether polyol is the polyalcohol that molecular weight is not higher than 2000 grams/mol;
The diisocyanate cpd is toluene di-isocyanate(TDI), methyl diphenylene diisocyanate, 1,6- hexa-methylenes Diisocyanate, isophorone diisocyanate, benzene dimethylene diisocyanate and cyclohexanedimethyleterephthalate diisocyanate In one kind or at least two;
The polyamine be containing there are two or more than two molecule of primary amine low molecular weight amine compound;
The sealer is containing carbonyl and the organic compound that can be reacted with the anti-raw Mannich of primary amine.
6. imine modified polyaspartic ester water proof anti-corrosive paint according to claim 1, it is characterised in that:
The polyaspartic ester is Bayer Desmophen NH1420, Bayer Desmophen NH1520, Bayer Desmophen NH1220, Zhuhai fly upward F-420, F-524 is flown upward in Zhuhai, F-520 is flown upward in Zhuhai and Zhuhai is flown upward one in F220 Kind or at least two.
7. imine modified polyaspartic ester water proof anti-corrosive paint according to claim 1, it is characterised in that:
The accelerating agent is dibutyl tin laurate, stannous octoate and one kind in isooctyl acid bismuth or at least two;
The filler be titanium dioxide, silicon powder, flyash, talcum powder, sericite in powder, blanc fixe, powdered whiting and One kind in precipitated calcium carbonate or at least two.
8. the preparation method of the imine modified polyaspartic ester water proof anti-corrosive paint of claim 1~7 any one of them, It is characterized in that including the following steps:
(1) polyaspartic ester, imines and accelerating agent are uniformly mixed, obtain first component;Wherein, each component presses quality percentage It is as follows than counting:Polyaspartic ester 46~61%, imines 38.5~53.5% and accelerating agent 0.1%~0.5%;
(2) by isocyanate functional group's component, low viscosity epoxy compound, nano fumed silica, filler, pigment and other Auxiliary agent is uniformly mixed, and obtains second component;Wherein, each component is as follows by mass percentage:Isocyanate functional group's component 50~ 61%, low viscosity epoxy compound 11~15%, nano fumed silica 5~8%, filler 18~27%, pigment 1% and its His auxiliary agent 2%.
9. the application of the imine modified polyaspartic ester water proof anti-corrosive paint of claim 1~7 any one of them, feature It is to include the following steps:By first component and component B in mass ratio 1:3~1:4.5 be uniformly mixed, be coated on sheet metal or Concrete construction surface.
10. the application of imine modified polyaspartic ester water proof anti-corrosive paint according to claim 9, feature exist In:
The concrete construction is the concrete construction of humidity;
The thickness for the film that the coating is formed is 1.5~2mm.
CN201610547533.0A 2016-07-11 2016-07-11 A kind of imine modified polyaspartic ester water proof anti-corrosive paint and preparation method and application Expired - Fee Related CN105949987B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610547533.0A CN105949987B (en) 2016-07-11 2016-07-11 A kind of imine modified polyaspartic ester water proof anti-corrosive paint and preparation method and application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610547533.0A CN105949987B (en) 2016-07-11 2016-07-11 A kind of imine modified polyaspartic ester water proof anti-corrosive paint and preparation method and application

Publications (2)

Publication Number Publication Date
CN105949987A CN105949987A (en) 2016-09-21
CN105949987B true CN105949987B (en) 2018-07-31

Family

ID=56899974

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610547533.0A Expired - Fee Related CN105949987B (en) 2016-07-11 2016-07-11 A kind of imine modified polyaspartic ester water proof anti-corrosive paint and preparation method and application

Country Status (1)

Country Link
CN (1) CN105949987B (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106854428B (en) * 2016-11-08 2019-11-05 山东非金属材料研究所 A kind of flexible polyurea anticorrosive paint
CN106811037B (en) * 2017-01-12 2019-04-23 广州嘉睿复合材料有限公司 A kind of Polyaspartic Polyurea coating and its application
CN107556451B (en) * 2017-08-22 2021-11-23 山西省建筑科学研究院 Macromolecular polyaspartic acid ester and preparation method thereof
CN107663407B (en) * 2017-10-25 2020-12-15 广东东方雨虹防水工程有限公司 Polyaspartate polyurea waterproof coating, preparation method thereof and repair construction method of indoor waterproof structure
CN108250944B (en) * 2017-12-28 2020-06-16 中冶建筑研究总院有限公司 Concrete coating protection system and construction method
CN109467571B (en) * 2018-09-29 2023-12-19 万华化学集团股份有限公司 Siloxane modified aspartic acid ester and preparation method and application thereof
CN110527084B (en) * 2019-05-12 2022-01-28 合肥博朗德纳米技术有限公司 Biodegradable L-structure polyaspartic acid high-molecular dispersant and preparation method thereof
CN112375196B (en) * 2020-11-12 2022-09-23 深圳飞扬骏研新材料股份有限公司 Polyurea resin and preparation method and application thereof
CN113637398B (en) * 2021-08-25 2022-03-08 黄山中邦孚而道涂料有限公司 Bottom-surface integrated solvent-free polyaspartic acid ester heavy-duty anticorrosive paint, and preparation method and application thereof
CN114262559B (en) * 2022-01-26 2022-08-23 深圳飞扬骏研新材料股份有限公司 Asparagus polyurea coating and preparation method thereof
CN114456691A (en) * 2022-01-26 2022-05-10 深圳飞扬骏研新材料股份有限公司 Method for prolonging activation period of asparagus polyurea coating and coating
CN118460089A (en) * 2024-07-04 2024-08-09 北京宇阳泽丽防水材料有限责任公司 Single-component transparent polyurea coating and preparation method thereof

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4327853A1 (en) * 1993-08-19 1995-02-23 Bayer Ag Process for the production of coatings
US6989421B2 (en) * 2003-07-02 2006-01-24 E. I. Dupont Denemours And Company Two component coating compositions and coatings produced therefrom
DE102005020269A1 (en) * 2005-04-30 2006-11-09 Bayer Materialscience Ag Binder mixtures of polyaspartic esters and sulfonate-modified polyisocyanates
CN101469246B (en) * 2007-12-27 2011-12-21 上海涂料有限公司技术中心 Preparation of polyaspartate polyurea waterproof coating material
DE102009007194A1 (en) * 2009-02-03 2010-08-05 Bayer Materialscience Ag Flexible coatings
WO2011126562A2 (en) * 2010-04-09 2011-10-13 Bayer Materialscience Llc Two-component, polyaspartic coating compositions
CN103031045B (en) * 2011-10-10 2015-08-19 珠海飞扬新材料股份有限公司 Solvent-free polyaspartic acid ester polyurea elastic waterproof paint

Also Published As

Publication number Publication date
CN105949987A (en) 2016-09-21

Similar Documents

Publication Publication Date Title
CN105949987B (en) A kind of imine modified polyaspartic ester water proof anti-corrosive paint and preparation method and application
CN109467571B (en) Siloxane modified aspartic acid ester and preparation method and application thereof
CA2439786C (en) Polymeric urea-urethane rheology control agent and preparation process
CN102906188B (en) Eco-friendly aqueous epoxy resins composition and use thereof
CN109354987B (en) Polyaspartic acid ester polyurea coating with moderate surface drying time and capable of adapting to environmental change, preparation method, use method and application
CN109456684A (en) A kind of Polyaspartic Polyurea protective coating, preparation method, application method and application with good corrosion resistance
CN109439160A (en) A kind of Polyaspartic Polyurea protective coating, preparation method, application method and application with enhancing mechanical performance
KR101740239B1 (en) Coating material for protecting surface of concrete structure having improved preventing injury from salt and neutralization
CN100582185C (en) Pipeline repaired mouth anti-corrosive primer coating having high adhesive bonding ability with thermal contraction belt
KR101687987B1 (en) Coating material for protecting surface of steel structure having improved preventing injury from salt and neutralization
KR101998601B1 (en) polyurea resin waterproof membrane composition for spray or roller type coating
CN107814915B (en) Modifying agent of coating, modified epoxy resin coating, and preparation method and application thereof
RU2010129449A (en) THERMAL CURING POLYESTER POWDER COMPOSITION
WO2008118567A2 (en) Polythioether amine resins and compositions comprising same
DE10260299A1 (en) Reactive systems, their manufacture and their use
JP6348589B2 (en) Curable polyurethane coating composition and method for preparing the same
CN113980563B (en) Method for preparing one-component semi-polyurea waterproof coating composition and one-component semi-polyurea waterproof coating composition
CN114410271B (en) Double-component polyurethane joint beautifying agent and preparation method and application thereof
CN102181226A (en) Carbamate coating serving as monocomponent nonvolatile solvent and preparation method thereof
CN108117832B (en) Dual-curing type one-component polyurea coating and preparation method thereof
CN103113809A (en) High-bonding strength base paint for wet concrete interface and preparation method thereof
JPS62109868A (en) Anticorrosive coating material for reinforced concrete
JP2001342339A (en) Water curable urethane resin composition, coating, coating material, sealing medium, adhesive, and method of producing cured product
JP3556092B2 (en) Primer composition for steel corrosion protection
CN115637096B (en) High-wear-resistance coating liquid composition and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20180731

Termination date: 20210711