CN102344569B - Preparation method of modified organic silicon resin and paint containing prepared modified organic silicon resin - Google Patents
Preparation method of modified organic silicon resin and paint containing prepared modified organic silicon resin Download PDFInfo
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- CN102344569B CN102344569B CN2011101736220A CN201110173622A CN102344569B CN 102344569 B CN102344569 B CN 102344569B CN 2011101736220 A CN2011101736220 A CN 2011101736220A CN 201110173622 A CN201110173622 A CN 201110173622A CN 102344569 B CN102344569 B CN 102344569B
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Abstract
The invention relates to the field of organic high molecular compounds, and particularly relates to a preparation method of modified organic silicon resin. The method comprises the following steps: sequentially heating 40-60w% of amino-terminated hyperbranched polyamide, 1-10w% of epoxy resin and 30-50w% of organic silicon resin along with a crosslinking catalyst accounting for 1-10w% of the amino-terminated hyperbranched polyamide respectively at 110-120 DEG C, 150-170 DEG C and 200-210 DEG C for 1-3 hours; and finally cooling to room temperature, and adding an organic solvent to regulate the solid content to 60-70%. The method combines the advantages of the hyperbranched polyamide, the epoxy resin and the organic silicon resin, and achieves excellent heat resistance, favorable metal adhesion, low surface energy and excellent water boiling resistance and alkaline resistance. The modified organic silicon resin prepared by the method can be used for preparing a high-temperature-resistant low-surface-energy paint.
Description
Technical field
The present invention relates to the organic high molecular compound field, relate to the macromolecular compound that only obtains, be specifically related to silicone resin with the silica reaction.
Background technology
Have in the silicone resin-the Si-O-Si-structure, demonstrate performances such as good weathering resistance, thermotolerance, anti-stain characteristic and chemically stable.But pure silicone resin needs hot setting, and long construction inconvenience set time, simultaneously with the poor adhesive force of metallic substance; Poor solvent resistance, physical strength are not high, cost an arm and a leg; So its use receives restriction to a certain degree, other resins therefore commonly used carry out modification to it.Other resins such as use epoxy resin carry out modification to silicone resin, can improve the metal sticking power of resin, hardness and mechanical property.For example use bisphenol A epoxide resin p-methylphenyl silicone resin such as Deng Ming mountain carries out modification, obtains fire resistant epoxy modified organic silicone resin (Deng Mingshan, golden double happiness; The Huanghai Sea, the development of epoxy modified silicone high-temperature resistant coating, Anhui chemical industry; 2000,103 (2), 27-29).But the epoxy modified silicone resin difference of hardness, mechanical property can not satisfy market demands.
Polyamide resin has good thermotolerance, wearability, chemical proofing and good mechanical performance and processing characteristics, and frictional coefficient is low, and certain flame retardant resistance is arranged, and is easy to processing, is widely used to be engineering plastics.The consistency of polymeric amide and various kinds of resin is good, in coating industry, is used widely.But the polyamide resin molecular weight is big, and is poorly soluble, and viscosity is high, and difficult and other resins carry out chemical modification.In order to obtain LV, the polyamide resin that solvability is good, use dimeracid commonly used and diamine polymerization.For example (chapter are deposited in punishment, the preparation of pure soluble polyamide, applied chemistry, 1995 (02), 104) such as chapters deposited in punishment) dimeracid, sebacic acid, quadrol and hydroxyl tn copolymerization are obtained low molecular polyamides.But the low-molecular-weight polyamide resin poor heat resistance of preparation, end group activation functional group content is few, can not improve the resistance toheat of other resins such as epoxy resin.
Hyperbranched polymer has highly branched structure and a large amount of end group reactive groups, has high resolution, LV and higher chemical reactivity, and these make hyperbranched polymer demonstrate tempting application prospect in many aspects.LV makes hyperbranched polymer be fit to be applied to high solid component coating, can reduce system viscosity with the blend of line polymer coating, and the improvement system is mobile; High solvability can reduce the consumption of solvent, reduces cost, and reduces noxious gas emission; It is less that highly branched structure makes that the hyperbranched polymer molecule interchain tangles, and is difficult for crystallization, makes coating have good film forming properties.But the molecular weight of filming that forms after the hyperbranched polymer film forming is low, and cross-linking density causes the bad mechanical property of filming for a short time, and chemical-resistant can meet the demands; The film coated surface that forms after the hyperbranched polymer film forming simultaneously contains abundant reactive group, reduces the water resistance of filming.
Summary of the invention
The technical problem that the present invention solves provides a kind of preparation method of modified organic silicone resin, and the modified organic silicone resin of this method preparation has the low and good advantage of alkaline-resisting water resistance of heat-resisting low surface energy.
The technical solution that the present invention addresses the above problem is:
A kind of preparation method of modified organic silicone resin, this method is made up of following steps:
The amine-terminated hyperbrancedization polymeric amide of 40～60w%, the epoxy resin of 1～10w% and the silicone resin of 30～50w% and the crosslinking catalyst that weight is amine-terminated hyperbrancedization polymeric amide consumption 1～10% are added in the reactor drum; Under 110～120 ℃, 150～170 ℃ and 200～210 ℃, heated respectively 1～3 hour successively; Reduce to room temperature at last, adding organic solvent adjustment solid content is 60～70%; In the above-mentioned steps,
The weight-average molecular weight of described amine-terminated hyperbrancedization polymeric amide is 2000～5000, and it is with trimeric cyanamide, diprotic acid and to contain the aminoalkyl group carboxylic acid be diprotic acid according to the ratio of amount of substance: trimeric cyanamide: contain aminoalkyl group carboxylic acid=1: 1～2: 0～0.1 and carry out amidate action and obtain; Wherein, described diprotic acid is m-phthalic acid, terephthalic acid, 1,6-hexanodioic acid and 1, and the 4-Succinic Acid is wherein a kind of or two or more; The described aminoalkyl group carboxylic acid that contains is that glycocoll, 3-alanine and 3-amino-2-methyl propionic acid are wherein a kind of or two or more;
Described epoxy resin is bicyclopentadiene dioxide, 3; 4-epoxidation naphthenic acid 3 '; 4 '-epoxidation hexanaphthene methyl esters, two ((3; The 4-epoxycyclohexyl) a kind of or two or more in adipic acid ester, two (2,3-oxirane ring amyl group) ether, bisphenol-s epoxy resin and TriMethylolPropane(TMP) glycidyl ether methyl);
Contain 2.5～15% methoxy or ethoxy and 3～20% hydroxyl in the described silicone resin, its weight-average molecular weight is 800～2000;
Described crosslinking catalyst is a kind of or two or more in tetrabutyl titanate, metatitanic acid four isobutylates, two octyloxy tin, two different octyloxy tin, two octyloxy zinc and the two different octyloxy zinc;
Described organic solvent is one or more in butanols, isopropylcarbinol, propylene glycol monomethyl ether, dipropylene glycol methyl ether, dipropylene glycol butyl ether, 1-Methoxy-2-propyl acetate, dipropylene glycol methyl ether acetate and the dipropylene glycol monobutyl ether acetate.
Employed silicone resin can be by the monomethyl triethoxyl silane in the aforesaid method, and the condensation reaction that is hydrolyzed of dimethyldiethoxysilane, siloxanes such as a phenyl triethoxy obtains, also can be by the monomethyl Trimethoxy silane; The condensation reaction that is hydrolyzed of dimethyldimethoxysil,ne, siloxanes such as a phenyl trimethoxy obtains, directly the mixture of one or more in the following specific product of use: the KR211 of company of SHIN-ETSU HANTOTAI; The KR212 of company of SHIN-ETSU HANTOTAI, the KR214 of company of SHIN-ETSU HANTOTAI, the KR216 of company of SHIN-ETSU HANTOTAI; The IC836 of Wa Ke company, the KR213 of company of SHIN-ETSU HANTOTAI, the KR9218 of company of SHIN-ETSU HANTOTAI; The KR217 of company of SHIN-ETSU HANTOTAI, 233 of Dow Corning Corporation, 249 of Dow Corning Corporation; The Z-6108 of Dow Corning Corporation, 3074 of Dow Corning Corporation, 3037 of Dow Corning Corporation.The hydrolysis-condensation reaction of above-mentioned siloxanes is the condensation reaction that is hydrolyzed of this area siloxanes commonly used, and its technology and reaction conditions are the routine techniquess that those skilled in the art should grasp.
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide of the present invention is preferably 3000～4000, and it better is to be prepared by following method: with diprotic acid, trimeric cyanamide with to contain the aminoalkyl group carboxylic acid be diprotic acid according to the amount of substance ratio: trimeric cyanamide: contain aminoalkyl group carboxylic acid=1: 1～1.4: 0.05～0.1 and add in the reactor drum; Per hour to heat up 20 ℃ rate of heating, be heated to 240 ℃, insulation 2～4h under 0.67～1.33kPa; Cool to room temperature; Wherein, described diprotic acid is m-phthalic acid, terephthalic acid and 1, and the 6-hexanodioic acid is wherein a kind of or two or more; The described aminoalkyl group carboxylic acid that contains is 3-alanine and wherein a kind of or mixture of 3-amino-2-methyl propionic acid.
Silicone resin of the present invention better be KR9218, the company of SHIN-ETSU HANTOTAI of KR213, the company of SHIN-ETSU HANTOTAI of IC836, the company of SHIN-ETSU HANTOTAI of KR216, the Wa Ke company of KR214, the company of SHIN-ETSU HANTOTAI of KR212, the company of SHIN-ETSU HANTOTAI of KR211, the company of SHIN-ETSU HANTOTAI of company of SHIN-ETSU HANTOTAI KR217, Dow Corning Corporation 233, Dow Corning Corporation 249,3037 wherein one or more kinds of mixtures of 3074 and Dow Corning Corporation of the Z-6108 of Dow Corning Corporation, Dow Corning Corporation.
Epoxy resin of the present invention is preferably bicyclopentadiene dioxide, 3; 4-epoxidation naphthenic acid 3 '; 4 '-epoxidation hexanaphthene methyl esters, two ((3; The 4-epoxycyclohexyl) methyl) adipic acid ester, two (2,3-oxirane ring amyl group) ether, bisphenol-s epoxy resin, TriMethylolPropane(TMP) glycidyl ether are wherein a kind of or two or more.
It is wherein a kind of or two or more that crosslinking catalyst of the present invention is preferably two octyloxy tin, two different octyloxy tin, two octyloxy zinc and two different octyloxy zinc.
Organic solvent of the present invention be preferably propylene glycol monomethyl ether, dipropylene glycol methyl ether, dipropylene glycol butyl ether, 1-Methoxy-2-propyl acetate, dipropylene glycol methyl ether acetate and dipropylene glycol monobutyl ether acetate one or more.
Among the preparation method of modified organic silicone resin of the present invention; Amine-terminated hyperbrancedization polymeric amide consumption is preferably 50～60w%; Content of epoxy resin is preferably 1～8w%; The silicone resin consumption is preferably 35～50w%, and the crosslinking catalyst consumption is preferably amine-terminated hyperbrancedization polymeric amide weight 1～5%.
Three kinds of crosslinking reactions take place among the preparation method of the present invention; First kind is that amino and the epoxy group(ing) on the epoxy resin on the amine-terminated hyperbrancedization polymeric amide carried out crosslinking reaction; Second kind is that silanol base and the epoxy group(ing) on the epoxy resin on the silicone resin carried out condensation reaction, and the third is that the hydroxyl that forms of amino and the epoxy reaction on the epoxy resin on the amine-terminated hyperbrancedization polymeric amide and the alkoxyl group on the silicone resin or silanol base carry out crosslinking reaction.Amine-terminated hyperbrancedization polymeric amide like this, epoxy resin and silicone resin carry out crosslinking reaction in twos; Form multiple cross-linked IPN pore network structure; The advantages of amine-terminated hyperbrancedization polymeric amide, epoxy resin and silicone resin is got up, and the modified organic silicone resin that is obtained has the following advantages:
(1) hyperbranched polymer has highly branched structure, and it is less to make that the hyperbranched polymer molecule interchain tangles, and the ultrabranching polyamide modified organic silicone resin of giving the present invention's preparation has the advantage of LV and good film forming properties.
(2) polymeric amide has good abrasion resistance, acid resistance and excellent mechanical property, and the ultrabranching polyamide modified organic silicone resin of giving the method for the invention preparation has favorable mechanical performance and alkaline resistance properties.
The method of the invention obtains modified organic silicone resin and can be used for preparing and have the good alkaline resistance properties and the coating of wear resisting property, contains the described modified organic silicone resin of 60～80w%, 10～20w% high-temperature resisting pigment filler and 5～20w% high boiling solvent in this coating.
High boiling solvent in the coating of the present invention is that divalent ester mixture, ethylene glycol ether acetate, Diethylene Glycol monobutyl ether acetate, isobutyl isobutyrate, propionic acid-3-ether ethyl ester, methyl isoamyl ketone are wherein a kind of or two or more.
High-temperature resisting pigment in the coating of the present invention can be inorganic high-temperature resistant pigment such as carbon black, iron oxide red, also can be organic high temperature-resistant pigment such as phthalocyanine blue.
In the coating of the present invention high temperature resistant filler, can be titanium oxide, silicon-dioxide and silit.
Coating of the present invention can also contain organosilicon auxiliary agents such as the silicone oil, polyethers of 1～5w%, as stepping the CoatOSil series polyethers of figure new high-tech material ltd.Described organosilicon auxiliary agent can play effects such as levelling, froth breaking, pigment wetting, viscosity adjustment.
The preparation method of coating of the present invention is this area preparation method commonly used, is about to modified organic silicone resin, pigment, filler, organosilicon auxiliary agent and high boiling solvent mixing and obtains.
Coating of the present invention has good heat-resistant, low surface energy, good water-fast solvent resistance and good metal sticking power; But applied metal surfacecti proteon; It is high temperature resistant to give metal; Anti-solvent, the characteristics of easy cleaning can be applied on the hardware products such as stove and accessory surface, barbecue grill, electriciron, cooker inside and outside wall.
The relative prior art of coating of the present invention has the following advantages: coating of the present invention with modified organic silicone resin as base resin; The amino ultrabranching polyamide of this resins process middle-end, epoxy resin and silicone resin carry out crosslinking reaction in twos; Form multiple cross-linked modified resin; The sticking power of amine-terminated hyperbrancedization polymeric amide is good; The advantage of the advantage that alkali resistance is good, the good mechanical property of epoxy resin and the low surface energy of silicone resin; Excellent heat resistance, the advantages that water resistance is good is got up, and therefore coating of the present invention has high heat resistance ability, good metal sticking power, low surface energy, the water boiling resistance of excellence and the advantage of alkaline resistance properties.
Embodiment
It below is the non-limiting example of technical scheme according to the invention.
Embodiment 1:
1) amine-terminated hyperbrancedization polymeric amide
A) form:
Trimeric cyanamide: 126g (1.0mol);
Diprotic acid: m-phthalic acid 57.1g (0.5mol); Terephthalic acid 49.8g (0.3mol); 1,6-hexanodioic acid 29g (0.2mol)
B) synthesis step:
Trimeric cyanamide and diprotic acid adding are equipped with heating, in the reactor drum of condensation and nitrogen protection, are warmed up to 110 ℃ under the nitrogen protection, insulation 2h; Be heated to 240 ℃ with 20 ℃ of rate of heating per hour, insulation 4h under 1.33kPa; Cool off room temperature at last, obtain amine-terminated hyperbrancedization of 220g polymeric amide.
C) performance of amine-terminated hyperbrancedization polymeric amide
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide adopts GPC to detect, and the result is 5001.
2) modified organic silicone resin
A) form:
Amine-terminated hyperbrancedization polymeric amide: the amine-terminated hyperbrancedization polyamide 6 0g of step 1 preparation;
Epoxy resin: bicyclopentadiene dioxide 10g;
Silicone resin: the silicone resin KR216 30g of SHIN-ETSU HANTOTAI;
Two octyloxy tin: 1g.
B) preparation technology:
Amine-terminated hyperbrancedization polymeric amide with step 1 preparation; Epoxy resin and silicone resin adding are equipped with in the reactor drum of heating, condensation and nitrogen protection device, add catalyzer, are warmed up to 120 ℃ of insulations 2 hours; Be warmed up to 160 ℃ of insulations 2 hours; Last cool to room temperature, adding 1-Methoxy-2-propyl acetate adjustment solid content is 70%, obtains modified organic silicone resin 132g.
C) modified organic silicone resin performance
The over-all properties of modified organic silicone resin
Resistance toheat: test piece behind 180 ℃ of baking 2h, is put into the Ovenized electric furnace that potentiometer is checked, by 5 ℃/min elevated temperature; Pick up counting to the requirement of experiment temperature with furnace temperature, sample takes out through behind the continuous high temperature; Be chilled to room temperature (25 ℃); Observe the coatingsurface situation with reading lens,, explain that promptly coating heat resistance can be good as not having be full of cracks, obscission.
3) coating
A) form
Modified organic silicone resin: the modified organic silicone resin 100g of step 2 preparation;
Paint filler: carbon black 40g; Titanium oxide 20g;
Organosilicon auxiliary agent: silicone oil
/350cst 8g;
High boiling solvent: divalent ester mixture (DBE) 5g.
B) preparation technology
Paint filler, modified organic silicone resin, organosilicon auxiliary agent, high boiling solvent are mixed, add grinding machine for grinding to required particle diameter, both.
C) performance
The performance index of coating
1* water boiling resistance performance: behind 180 ℃ of baking 2h, cool to room temperature is positioned over test piece in 100 ℃ the zero(ppm) water then with test piece, is heated to paint film and destroys, and occurs as bubbles loss of gloss, variable color, phenomenons such as be full of cracks.
2* resistance toheat: test piece behind 180 ℃ of baking 2h, is put into the Ovenized electric furnace that potentiometer is checked, by 5 ℃/min elevated temperature; Pick up counting to the requirement of experiment temperature with furnace temperature, sample takes out through behind the continuous high temperature; Be chilled to room temperature (25 ℃); Observe the coatingsurface situation with reading lens,, explain that promptly coating heat resistance can be good as not having be full of cracks, obscission.
3* surface tension: under 25 ℃, measure by the stalagmometry appearance.
Embodiment 2:
1) amine-terminated hyperbrancedization polymeric amide
A) form:
Trimeric cyanamide: 252g (2.0mol);
Diprotic acid: m-phthalic acid 99.6g (0.6mol); 1,4-Succinic Acid 23.6g (0.2mol); 1,6-hexanodioic acid 29g (0.2mol);
B) synthesis step:
Trimeric cyanamide and diprotic acid adding are equipped with heating, in the reactor drum of condensation and nitrogen protection, are warmed up to 110 ℃ under the nitrogen protection, insulation 2h; Be heated to 240 ℃ with 20 ℃ of rate of heating per hour, insulation 2h under 0.66kPa; Cool off room temperature at last, obtain amine-terminated hyperbrancedization of 364g polymeric amide.
C) performance of amine-terminated hyperbrancedization polymeric amide
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide adopts GPC to detect, and the result is 1992.
2) modified organic silicone resin
A) form:
Amine-terminated hyperbrancedization polymeric amide: the amine-terminated hyperbrancedization polymeric amide 40g of step 1 preparation;
Epoxy resin: TriMethylolPropane(TMP) glycidyl ether 8g;
Silicone resin: DOW CORNING 3037 52g;
Catalyzer: two octyloxy tin 3g.
B) preparation technology:
Saturated amine-terminated hyperbrancedization polymeric amide, epoxy resin and the silicone resin adding of step 1 preparation are equipped with in the reactor drum of heating, condensation and nitrogen protection device; Add catalyzer; Be warmed up to 110 ℃ of insulations 3 hours, be warmed up to 170 ℃ of insulations 1 hour, last cool to room temperature; Adding 1-Methoxy-2-propyl acetate adjustment solid content is 60%, obtains modified organic silicone resin 160g.
C) modified organic silicone resin performance
The over-all properties of modified organic silicone resin
3) coating
A) form
Modified organic silicone resin: the modified organic silicone resin 160g of step 2 preparation;
Paint filler: carbon black 20g;
High boiling solvent: divalent ester mixture (DBE) 5g; Ethylene glycol ether acetate (CAC): 5g.
B) preparation technology
Paint filler, modified organic silicone resin, high boiling solvent are mixed, add grinding machine for grinding to required particle diameter, both.
C) performance
The performance index of coating
Embodiment 3:
1) amine-terminated hyperbrancedization polymeric amide
A) form:
Trimeric cyanamide: 176.4g (1.4mol);
Diprotic acid: terephthalic acid 132.8g (0.8mol); 1,6-hexanodioic acid 29.2g (0.2mol);
Contain the aminoalkyl group carboxylic acid: glycocoll 3.75g (0.05mol); 3-alanine 4.45g (0.05mol)
B) synthesis step:
With trimeric cyanamide, diprotic acid with contain the aminoalkyl group carboxylic acid and add heating is housed, in the reactor drum of condensation and nitrogen protection, be warmed up to 110 ℃ under the nitrogen protection, be incubated 2h; Be heated to 240 ℃ with 20 ℃ of rate of heating per hour, insulation 2.5h under 0.78kPa; Cool off room temperature at last, obtain amine-terminated hyperbrancedization of 304g polymeric amide.
C) performance of amine-terminated hyperbrancedization polymeric amide
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide adopts GPC to detect, and the result is 3012.
2) silicone resin midbody
A) form
Monomethyl Trimethoxy silane: 42.0g (0.28mol)
Dimethyldimethoxysil,ne: 18.7g (0.14mol)
One phenyltrimethoxysila,e: 123.0g (0.58mol),
B) preparation technology
After in the reactor drum that prolong, TM, tap funnel and whisking appliance are housed, adding siloxanes and 4.5mmol hydrochloric acid successively, begin to stir and heat up, keep homo(io)thermism after being warmed up to 60 ℃ by proportioning; Under agitation drip 31.7g zero(ppm) water, after dropwising, again behind the isothermal reaction 3h; The beginning underpressure distillation, pressure-controlling boils off the small molecules that produces in the reaction process at 0.06MPa; Cool to room temperature, the adjustment solid content is 60%, obtains silicone resin midbody 290g.
C) performance
The weight-average molecular weight of silicone resin midbody adopts GPC to detect, and the result is 802; The hydroxy radical content of silicone resin midbody adopts the diacetyl oxide method to measure, and the result is 10.6%; The methoxy content of silicone resin midbody adopts perchloric acid acetyl method to measure, and the result is 7.4%; R/Si=1.14; Ph/Me=1.04.
3) modified organic silicone resin
A) form
Amine-terminated hyperbrancedization polymeric amide: the amine-terminated hyperbrancedization polymeric amide 50g of step 1 preparation;
Epoxy resin: two ((3, the 4-epoxycyclohexyl) methyl) adipic acid ester 4g; Bisphenol-s epoxy resin 2g;
Silicone resin: the silicone resin 73.3g of the solid content 60% of step 2 preparation;
Catalyzer: two different octyloxy tin 2.7g.
B) preparation technology
Amine-terminated hyperbrancedization polymeric amide with step 1 preparation; Epoxy resin and silicone resin adding are equipped with in the reactor drum of heating, condensation and nitrogen protection device, add catalyzer, are warmed up to 115 ℃ of insulations 1.5 hours; Be warmed up to 175 ℃ of insulations 1.5 hours; Last cool to room temperature, adding dipropylene glycol methyl ether acetate and dipropylene glycol monobutyl ether acetate adjustment solid content is 65%, obtains modified organic silicone resin 141g.
C) modified organic silicone resin performance
The over-all properties of modified organic silicone resin
4) coating
A) form
Modified organic silicone resin: the modified organic silicone resin 100g of step 3 preparation;
Paint filler: phthalocyanine blue 20g; Silicon-dioxide 20g;
Organosilicon auxiliary agent: CoatOSil 7001 4g; Silicone oil
/350cst 6g;
High boiling solvent: Diethylene Glycol monobutyl ether acetate (DBA) 5g; Ethylene glycol ether acetate (CAC) 5g.
B) preparation technology
Paint filler, modified organic silicone resin, organosilicon auxiliary agent, high boiling solvent are mixed, add grinding machine for grinding to required particle diameter, both.
C) be coated with performance
The performance index of coating
Embodiment 4:
1) amine-terminated hyperbrancedization polymeric amide
A) form:
Polyvalent alcohol: 227g (1.8mol);
Diprotic acid: m-phthalic acid 132.8g (0.8mol); 1,4-tetramethylenediamine 23.6g (0.2mol);
Contain the aminoalkyl group carboxylic acid: glycocoll 0.75g (0.01mol); 3-alanine 1.78g (0.02mol); 3-amino-2-methyl propionic acid 3.63g (0.03mol);
B) synthesis step:
With trimeric cyanamide, diprotic acid with contain the aminoalkyl group carboxylic acid and add heating is housed, in the reactor drum of condensation and nitrogen protection, be warmed up to 110 ℃ under the nitrogen protection, be incubated 2h; Be heated to 240 ℃ with 20 ℃ of rate of heating per hour, insulation 3.5h under 0.85kPa; Cool off room temperature at last, obtain amine-terminated hyperbrancedization of 348g polymeric amide.
C) performance of amine-terminated hyperbrancedization polymeric amide
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide adopts GPC to detect, and the result is 2139.
2) modified organic silicone resin
A) form
Amine-terminated hyperbrancedization polymeric amide: the amine-terminated hyperbrancedization polymeric amide 58g of step 1 preparation;
Epoxy resin: two (2,3-oxirane ring amyl group) ether 4g; 3,4-epoxidation naphthenic acid 3 ', 4 '-epoxidation hexanaphthene methyl esters 3g;
Silicone resin: the silicone resin KR211 15g of SHIN-ETSU HANTOTAI; The silicone resin KR214 20g of SHIN-ETSU HANTOTAI;
Catalyzer: two different octyloxy zinc 2g; Two octyloxy tin 1.5g.
B) preparation technology:
Amine-terminated hyperbrancedization polymeric amide with step 1 preparation; Epoxy resin and silicone resin adding are equipped with in the reactor drum of heating, condensation and nitrogen protection device, add catalyzer, are warmed up to 120 ℃ of insulations 2 hours; Be warmed up to 155 ℃ of insulations 2.5 hours; Last cool to room temperature, adding 1-Methoxy-2-propyl acetate and butanols adjustment solid content is 70%, obtains modified organic silicone resin 125g.
C) modified organic silicone resin performance
The over-all properties of modified organic silicone resin
3) coating
A) form
Modified organic silicone resin: the modified organic silicone resin 120g of step 2 preparation;
Paint filler: silit 10g; Silica 1 0g;
Organosilicon auxiliary agent: CoatOSil 3500 4g; Silicone oil
/350cst 4g;
High boiling solvent: propionic acid-3-ether ethyl ester (EEP) 10g; Divalent ester mixture (DBE) 10g.
B) preparation technology
Paint filler, modified organic silicone resin, organosilicon auxiliary agent, high boiling solvent are mixed, add grinding machine for grinding to required particle diameter, both.
C) performance
The performance index of coating
Embodiment 5
1) amine-terminated hyperbrancedization polymeric amide
A) form:
Trimeric cyanamide: 151g (1.2mol);
Diprotic acid: terephthalic acid 116.2g (0.7mol); 1,6-hexanediamine 29.2g (0.2mol); 1,4-Succinic Acid 11.8g (0.1mol);
Contain the amino 2 Methylpropionic acid 6.06g (0.05mol) of aminoalkyl group carboxylic acid: 3-;
B) synthesis step:
With trimeric cyanamide, diprotic acid with contain the aminoalkyl group carboxylic acid and add heating is housed, in the reactor drum of condensation and nitrogen protection, be warmed up to 110 ℃ under the nitrogen protection, be incubated 2h; Be heated to 240 ℃ with 20 ℃ of rate of heating per hour, insulation 2.5h under 0.66kPa; Cool off room temperature at last, obtain amine-terminated hyperbrancedization of 274g polymeric amide.
C) performance of amine-terminated hyperbrancedization polymeric amide
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide adopts GPC to detect, and the result is 3995.
2) modified organic silicone resin
A) form:
Amine-terminated hyperbrancedization polymeric amide: the amine-terminated hyperbrancedization polymeric amide 45g of step 1 preparation;
Epoxy resin: two ((3, the 4-epoxycyclohexyl) methyl) adipic acid ester 4g; 3,4-epoxidation naphthenic acid 3 ', 4 '-epoxidation hexanaphthene methyl esters 4g; Bicyclopentadiene dioxide 2g;
Silicone resin: silicone resin 233 35g of Dow Corning Corporation; Silicone resin 249 10g of Dow Corning Corporation;
Catalyzer: two octyloxy tin 3.5g.
B) preparation technology:
Amine-terminated hyperbrancedization polymeric amide with step 1 preparation; Epoxy resin and silicone resin adding are equipped with in the reactor drum of heating, condensation and nitrogen protection device, add catalyzer, are warmed up to 130 ℃ of insulations 1 hour; Be warmed up to 170 ℃ of insulations 1 hour; Last cool to room temperature, adding isopropylcarbinol and propylene glycol monomethyl ether adjustment solid content is 65%, obtains modified organic silicone resin 141g.
C) modified organic silicone resin performance
The over-all properties of modified organic silicone resin
3) coating
A) form
Modified organic silicone resin: the modified organic silicone resin 140g of step 2 preparation;
Paint filler: carbon black 20g; Silica 1 4g;
Organosilicon auxiliary agent: CoatOSil 3500 4g; CoatOSil 7650 2g;
High boiling solvent: methyl isoamyl ketone (MIAK) 2g; Isobutyl isobutyrate 4g.
B) preparation technology
Paint filler, modified organic silicone resin, organosilicon auxiliary agent, high boiling solvent are mixed, add grinding machine for grinding to required particle diameter, both.
C) performance
The performance index of coating
Embodiment 6
1) amine-terminated hyperbrancedization polymeric amide
A) form:
Trimeric cyanamide: 189g (1.5mol);
Diprotic acid: terephthalic acid 141g (0.85mol); 1,6-hexanediamine 21.9g (0.15mol);
Contain the aminoalkyl group carboxylic acid: 3-amino-2-methyl propionic acid 1.21g (0.01mol); 3-alanine 0.89g (0.01mol).
B) synthesis step:
With trimeric cyanamide, diprotic acid with contain the aminoalkyl group carboxylic acid and add heating is housed, in the reactor drum of condensation and nitrogen protection, be warmed up to 110 ℃ under the nitrogen protection, be incubated 2h; Be heated to 240 ℃ with 20 ℃ of rate of heating per hour, insulation 4h under 1.33kPa; Cool off room temperature at last, obtain amine-terminated hyperbrancedization of 312g polymeric amide.
C) performance of amine-terminated hyperbrancedization polymeric amide
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide adopts GPC to detect, and the result is 3673.
2) modified organic silicone resin
A) form
Amine-terminated hyperbrancedization polymeric amide: the amine-terminated hyperbrancedization polymeric amide 49g of step 1 preparation;
Epoxy resin: bicyclopentadiene dioxide 1g;
Silicone resin: DOW CORNING silicone resin 3074 35g; The silicone resin KR212 15g of SHIN-ETSU HANTOTAI;
Catalyzer: two octyloxy tin 1g; Tetrabutyl titanate 1g.
B) preparation technology
Amine-terminated hyperbrancedization polymeric amide with step 1 preparation; Epoxy resin and silicone resin adding are equipped with in the reactor drum of heating, condensation and nitrogen protection device, add catalyzer, are warmed up to 125 ℃ of insulations 2 hours; Be warmed up to 155 ℃ of insulations 2.5 hours; Last cool to room temperature, adding 1-Methoxy-2-propyl acetate and dipropylene glycol methyl ether adjustment solid content is 60%, obtains modified organic silicone resin 144g.
C) modified organic silicone resin performance
The over-all properties of modified organic silicone resin
3) coating
A) form
Modified organic silicone resin: the modified organic silicone resin 120g of step 2 preparation;
Paint filler: carbon black 20g; Silicon-dioxide 5g; Titanium oxide 5g;
Organosilicon auxiliary agent: CoatOSil 3500 4g; CoatOSil 7510 2g; Silicone oil
/350cst 4g;
High boiling solvent: divalent ester mixture (DBE) 12g.
B) preparation technology
Paint filler, modified organic silicone resin, organosilicon auxiliary agent, high boiling solvent are mixed, add grinding machine for grinding to required particle diameter, both.
C) performance
The performance index of coating
Embodiment 7
1) amine-terminated hyperbrancedization polymeric amide
A) form
Trimeric cyanamide: 126g (1.0mol);
Diprotic acid: m-phthalic acid 124.5g (0.75mol); 1,6-hexanodioic acid 36.5g (0.25mol)
Contain the amino 2 Methylpropionic acid 1.21g (0.01mol) of aminoalkyl group carboxylic acid: 3-;
B) synthesis step:
With trimeric cyanamide, diprotic acid with contain the aminoalkyl group carboxylic acid and add heating is housed, in the reactor drum of condensation and nitrogen protection, be warmed up to 110 ℃ under the nitrogen protection, be incubated 2h; Be heated to 240 ℃ with 20 ℃ of rate of heating per hour, insulation 3.5h under 1.03kPa; Cool off room temperature at last, obtain amine-terminated hyperbrancedization of 248g polymeric amide.
C) performance of amine-terminated hyperbrancedization polymeric amide
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide adopts GPC to detect, and the result is 4702.
2) modified organic silicone resin
A) form
Amine-terminated hyperbrancedization polymeric amide: the amine-terminated hyperbrancedization polymeric amide 48g of step 1 preparation;
Epoxy resin: TriMethylolPropane(TMP) glycidyl ether 2g; 3,4-epoxidation naphthenic acid 3 ', 4 '-epoxidation hexanaphthene methyl esters 1g; Bisphenol-s epoxy resin 1g;
Silicone resin: the silicone resin IC836 20g of Wa Ke company; The silicone resin Z-6108 10g of Dow Corning Corporation; The silicone resin KR213 18g of company of SHIN-ETSU HANTOTAI;
Catalyzer: metatitanic acid four isobutylate 0.3g; Two octyloxy tin 0.2g.
B) preparation technology
Amine-terminated hyperbrancedization polymeric amide with step 1 preparation; Epoxy resin and silicone resin adding are equipped with in the reactor drum of heating, condensation and nitrogen protection device, add catalyzer, are warmed up to 130 ℃ of insulations 1 hour; Be warmed up to 150 ℃ of insulations 3 hours; Last cool to room temperature, adding 1-Methoxy-2-propyl acetate and dipropylene glycol butyl ether adjustment solid content is 70%, obtains modified organic silicone resin 126g.
C) modified organic silicone resin performance
The over-all properties of modified organic silicone resin
3) coating
A) form
Modified organic silicone resin: the modified organic silicone resin 110g of step 2 preparation;
Paint filler: phthalocyanine blue 20g; Silicon-dioxide 5g; Titanium oxide 5g;
High boiling solvent: divalent ester mixture (DBE) 40g; Isobutyl isobutyrate 20g.
B) preparation technology
Paint filler, modified organic silicone resin, organosilicon auxiliary agent, high boiling solvent are mixed, add grinding machine for grinding to required particle diameter, both.
C) performance
The performance index of coating
Embodiment 8
1) amine-terminated hyperbrancedization polymeric amide
A) form:
Trimeric cyanamide: 199.2g (1.0mol)
Diprotic acid: m-phthalic acid 149.4g (0.9mol); 1,6-hexanodioic acid 14.6g (0.1mol)
Contain the aminoalkyl group carboxylic acid: 3-alanine 8.9g (0.1mol).
B) synthesis step:
With trimeric cyanamide, diprotic acid with contain the aminoalkyl group carboxylic acid and add heating is housed, in the reactor drum of condensation and nitrogen protection, be warmed up to 110 ℃ under the nitrogen protection, be incubated 2h; Be heated to 240 ℃ with 20 ℃ of rate of heating per hour, insulation 4h under 1.33kPa; Cool off room temperature at last, obtain amine-terminated hyperbrancedization of 322g polymeric amide.
C) performance of amine-terminated hyperbrancedization polymeric amide
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide adopts GPC to detect, and the result is 3897.
2) silicone resin
A) form
Monomethyl triethoxyl silane: 69.1g (0.36mol)
Dimethyldiethoxysilane: 34.0g (0.21mol)
One phenyl triethoxysilane: 109.24g (0.43mol),
B) preparation technology
After in the reactor drum that prolong, TM, tap funnel and whisking appliance are housed, adding siloxanes and 5.5mmol hydrochloric acid successively, begin to stir and heat up, keep homo(io)thermism after being warmed up to 70 ℃ by proportioning; Under agitation drip 42.7g zero(ppm) water, after dropwising, again behind the isothermal reaction 3h; The beginning underpressure distillation, pressure-controlling boils off the small molecules that produces in the reaction process at 0.06MPa; Cool to room temperature, the adjustment solid content is 60%, obtains silicone resin midbody 322g.
C) performance
The weight-average molecular weight of silicone resin midbody adopts GPC to detect, and the result is 1808; The hydroxy radical content of silicone resin midbody adopts the diacetyl oxide method to measure, and the result is 20%; The oxyethyl group content of silicone resin midbody adopts perchloric acid acetyl method to measure, and the result is 2.5%; R/Si=1.21; Ph/Me=0.55.
3) modified organic silicone resin
A) form
Amine-terminated hyperbrancedization polymeric amide: the amine-terminated hyperbrancedization polymeric amide 56g of step 1 preparation;
Epoxy resin: bicyclopentadiene dioxide 9g;
Silicone resin: step 2 synthetic silicone resin 35g
Catalyzer: two octyloxy zinc 2.5g; Two octyloxy tin 2g.
B) preparation technology
Amine-terminated hyperbrancedization polymeric amide with step 1 preparation; Epoxy resin and silicone resin adding are equipped with in the reactor drum of heating, condensation and nitrogen protection device, add catalyzer, are warmed up to 110 ℃ of insulations 3 hours; Be warmed up to 150 ℃ of insulations 3 hours; Last cool to room temperature, adding 1-Methoxy-2-propyl acetate adjustment solid content is 65%, obtains modified organic silicone resin 138g.
C) modified organic silicone resin performance
The over-all properties of modified organic silicone resin
4) coating
A) form
Modified organic silicone resin: the modified organic silicone resin 150g of step 2 preparation;
Paint filler: carbon black 10g; Silicon-dioxide 5g; Titanium oxide 5g;
Organosilicon auxiliary agent: CoatOSil 3500 5g; Silicone oil
/350cst 5g;
High boiling solvent: divalent ester mixture (DBE) 10g.
B) preparation technology
Paint filler, modified organic silicone resin, organosilicon auxiliary agent, high boiling solvent are mixed, add grinding machine for grinding to required particle diameter, both.
C) performance
The performance index of coating
Embodiment 9
1) amine-terminated hyperbrancedization polymeric amide becomes
A) form
Trimeric cyanamide: 176.4g (1.4mol);
Diprotic acid: m-phthalic acid 132.8g (0.8mol); 1,6-hexanodioic acid 29.2g (0.2mol)
B) synthesis step
Trimeric cyanamide and diprotic acid adding are equipped with heating, in the reactor drum of condensation and nitrogen protection, are warmed up to 110 ℃ under the nitrogen protection, insulation 2h; Be heated to 240 ℃ with 20 ℃ of rate of heating per hour, insulation 4h under 1.33kPa; Cool off room temperature at last, obtain amine-terminated hyperbrancedization of 300g polymeric amide.
C) performance of amine-terminated hyperbrancedization polymeric amide
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide adopts GPC to detect, and the result is 3173.
2) silicone resin
A) form
Monomethyl triethoxyl silane: 44.5g (0.25mol)
Dimethyldiethoxysilane: 50.3g (0.34mol)
One phenyl triethoxysilane: 98.4g (0.41mol),
B) preparation technology
After in the reactor drum that prolong, TM, tap funnel and whisking appliance are housed, adding siloxanes and 7.0mmol hydrochloric acid successively, begin to stir and heat up, keep homo(io)thermism after being warmed up to 70 ℃ by proportioning; Under agitation drip 43.1g zero(ppm) water, after dropwising, again behind the isothermal reaction 3h; The beginning underpressure distillation, pressure-controlling boils off the small molecules that produces in the reaction process at 0.06MPa; Cool to room temperature, the adjustment solid content is 80%, obtains silicone resin midbody 230g.
C) performance
The weight-average molecular weight of silicone resin midbody adopts GPC to detect, and the result is 1986; The hydroxy radical content of silicone resin midbody adopts the diacetyl oxide method to measure, and the result is 15%; The oxyethyl group content of silicone resin midbody adopts perchloric acid acetyl method to measure, and the result is 3%; R/Si=1.34; Ph/Me=0.44.
3) modified organic silicone resin
A) form
Amine-terminated hyperbrancedization polymeric amide: the amine-terminated hyperbrancedization kymene 2g of step 1 preparation;
Epoxy resin: bicyclopentadiene dioxide 8g;
Silicone resin: step 2 synthetic 60% solid content silicone resin 100g;
Catalyzer: two octyloxy tin 1g, two different octyloxy tin 0.6g.
B) preparation technology
Amine-terminated hyperbrancedization polymeric amide with step 1 preparation; Epoxy resin and silicone resin adding are equipped with in the reactor drum of heating, condensation and nitrogen protection device, add catalyzer, are warmed up to 125 ℃ of insulations 2 hours; Be warmed up to 160 ℃ of insulations 2 hours; Last cool to room temperature, adding 1-Methoxy-2-propyl acetate adjustment solid content is 60%, obtains modified organic silicone resin 148g.
C) modified organic silicone resin performance
The over-all properties of modified organic silicone resin
4) coating
A) form
Modified organic silicone resin: the modified organic silicone resin 150g of step 2 preparation;
Paint filler: phthalocyanine blue 20g; Titanium oxide 20g;
Organic additive: CoatOSil 7510 8g;
Height boils and reaches solvent: divalent ester mixture (DBE) 2g.
B) preparation technology
Paint filler, modified organic silicone resin, organosilicon auxiliary agent, high boiling solvent are mixed, add grinding machine for grinding to required particle diameter, both.
C) performance
The performance index of coating
Embodiment 10
1) amine-terminated hyperbrancedization polymeric amide
A) form:
Trimeric cyanamide: 138.6g (1.1mol);
Diprotic acid: m-phthalic acid 141g (0.85mol); 1,6-hexanodioic acid 21.9g (0.15mol)
B) synthesis step:
Trimeric cyanamide and diprotic acid adding are equipped with heating, in the reactor drum of condensation and nitrogen protection, are warmed up to 110 ℃ under the nitrogen protection, insulation 2h; Be heated to 240 ℃ with 20 ℃ of rate of heating per hour, insulation 2h under 0.66kPa; Cool off room temperature at last, obtain amine-terminated hyperbrancedization of 258g polymeric amide.
C) performance of amine-terminated hyperbrancedization polymeric amide
The weight-average molecular weight of amine-terminated hyperbrancedization polymeric amide adopts GPC to detect, and the result is 3961.
2) modified organic silicone resin
A) form:
Amine-terminated hyperbrancedization polymeric amide: the amine-terminated hyperbrancedization polymeric amide 51g of step 1 preparation;
Epoxy resin: TriMethylolPropane(TMP) glycidyl ether 1g; Two (2,3-oxirane ring amyl group) ether 3g;
Silicone resin: the silicone resin KR9218 25g of SHIN-ETSU HANTOTAI; DOW CORNING silicone resin Z-6108 20g;
Catalyzer: two octyloxy zinc 0.6g; Two different octyloxy zinc 0.41g.
B) preparation technology:
Amine-terminated hyperbrancedization polymeric amide with step 1 preparation; Epoxy resin and silicone resin adding are equipped with in the reactor drum of heating, condensation and nitrogen protection device, add catalyzer, are warmed up to 120 ℃ of insulations 2 hours; Be warmed up to 175 ℃ of insulations 2 hours; Last cool to room temperature, adding 1-Methoxy-2-propyl acetate adjustment solid content is 65%, obtains modified organic silicone resin 136g.
C) modified organic silicone resin performance
The over-all properties of modified organic silicone resin
3) coating
A) form
Modified organic silicone resin: the modified organic silicone resin 120g of step 2 preparation;
Paint filler: iron oxide red 30g; Titanium oxide 20g; Silica 1 0g;
Organosilicon auxiliary agent: CoatOSil 7510:2g;
High boiling solvent: divalent ester mixture (DBE): 18g.
B) preparation technology
Paint filler, modified organic silicone resin, organosilicon auxiliary agent, high boiling solvent are mixed, add grinding machine for grinding to required particle diameter, both.
C) performance
The performance index of coating
Claims (5)
1. the preparation method of a modified organic silicone resin, this method is made up of following steps:
The crosslinking catalyst that silicone resin and the weight of amine-terminated hyperbrancedization of 40～60wt% polymeric amide, 1～10wt% epoxy resin and 30～50wt% is amine-terminated hyperbrancedization polymeric amide consumption 1～10% adds in the reactor drum; Under 110～120 ℃, 150～170 ℃ and 200～210 ℃, heated respectively 1～3 hour successively; Reduce to room temperature at last, adding organic solvent adjustment solid content is 60～70%; In the above-mentioned steps,
The weight-average molecular weight of described amine-terminated hyperbrancedization polymeric amide is 2000～5000, and it is with trimeric cyanamide, diprotic acid and to contain the aminoalkyl group carboxylic acid be diprotic acid according to the ratio of amount of substance: trimeric cyanamide: contain aminoalkyl group carboxylic acid=1: 1～2: 0～0.1 and carry out amidate action and obtain; Wherein, described diprotic acid is m-phthalic acid, terephthalic acid, 1,6-hexanodioic acid and 1, and the 4-Succinic Acid is wherein a kind of or two or more; The described aminoalkyl group carboxylic acid that contains is that glycocoll, 3-alanine and 3-amino-2-methyl propionic acid are wherein a kind of or two or more;
Described epoxy resin is bicyclopentadiene dioxide, 3; 4-epoxidation naphthenic acid 3 '; 4 '-epoxidation hexanaphthene methyl esters, two ((3; The 4-epoxycyclohexyl) methyl) adipic acid ester, two (2,3-oxirane ring amyl group) ether, bisphenol-s epoxy resin and TriMethylolPropane(TMP) glycidyl ether are wherein a kind of or two or more;
Contain 2.5～15% methoxy or ethoxy and 3～20% hydroxyl in the described silicone resin, its weight-average molecular weight is 800～2000;
Described crosslinking catalyst is a kind of or two or more in tetrabutyl titanate, metatitanic acid four isobutylates, two octyloxy tin, two different octyloxy tin, two octyloxy zinc and the two different octyloxy zinc;
Described organic solvent is one or more in butanols, isopropylcarbinol, propylene glycol monomethyl ether, dipropylene glycol methyl ether, dipropylene glycol butyl ether, 1-Methoxy-2-propyl acetate, dipropylene glycol methyl ether acetate and the dipropylene glycol monobutyl ether acetate.
2. the preparation method of the described modified organic silicone resin of claim 1; It is characterized in that; Described amine-terminated hyperbrancedization polymeric amide consumption is 50～60wt%; Described content of epoxy resin is 1～8wt%, and described silicone resin consumption is 35～50wt%, and described crosslinking catalyst consumption is 1～5% of an amine-terminated hyperbrancedization polymeric amide weight.
3. the preparation method of the described modified organic silicone resin of claim 1; It is characterized in that, described silicone resin be KR9218, the company of SHIN-ETSU HANTOTAI of KR213, the company of SHIN-ETSU HANTOTAI of IC836, the company of SHIN-ETSU HANTOTAI of KR216, the Wa Ke company of KR214, the company of SHIN-ETSU HANTOTAI of KR212, the company of SHIN-ETSU HANTOTAI of KR211, the company of SHIN-ETSU HANTOTAI of company of SHIN-ETSU HANTOTAI KR217, Dow Corning Corporation 233, Dow Corning Corporation 249,3074 and Dow Corning Corporation of the Z-6108 of Dow Corning Corporation, Dow Corning Corporation 3037 in a kind of or two or more.
4. the preparation method of the described modified organic silicone resin of claim 1; It is characterized in that; The weight-average molecular weight of described amine-terminated hyperbrancedization polymeric amide is 3000～4000; It is with diprotic acid, trimeric cyanamide and to contain the aminoalkyl group carboxylic acid be diprotic acid according to the amount of substance ratio: trimeric cyanamide: contain aminoalkyl group carboxylic acid=1: 1～1.4: 0.05～0.1 and add and carry out reactions in the reactor drum and obtain: per hour to heat up 20 ℃ rate of heating; Be heated to 240 ℃, insulation 2～4h under 0.67～1.33kPa; Cool to room temperature obtains; Wherein, described diprotic acid is m-phthalic acid, terephthalic acid and 1, and the 6-hexanodioic acid is wherein a kind of or two or more; The described aminoalkyl group carboxylic acid that contains is 3-alanine and wherein a kind of or mixture of 3-amino-2-methyl propionic acid.
5. coating, this coating contain modified organic silicone resin, 10～20wt% high-temperature resisting pigment filler and 5～20wt% high boiling solvent of one of them said method preparation of 60～80wt% claim 1 to 4; Wherein, described high boiling solvent is meant that divalent ester mixture, ethylene glycol ether acetate, Diethylene Glycol monobutyl ether acetate, isobutyl isobutyrate, propionic acid-3-ether ethyl ester and methyl isoamyl ketone are wherein a kind of or two or more.
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| CN102977363B (en) * | 2012-11-27 | 2015-01-21 | 南方医科大学 | Preparation method of modified amino-terminated hyper-branched polyamide resin and coating comprising resin |
| CN103073718B (en) * | 2013-01-31 | 2015-03-11 | 华南理工大学 | Amino-terminated silicon oil modified amino-terminated hyperbranched polyamide resin and preparation method and application of polyamide resin |
| CN106634582A (en) * | 2016-12-09 | 2017-05-10 | 桂林加宏汽车修理有限公司 | Anti-freezing coating |
| CN106634581A (en) * | 2016-12-09 | 2017-05-10 | 桂林加宏汽车修理有限公司 | Antistatic paint |
| CN106700922A (en) * | 2016-12-09 | 2017-05-24 | 桂林加宏汽车修理有限公司 | Environment-friendly coating |
| CN106700923A (en) * | 2016-12-09 | 2017-05-24 | 桂林加宏汽车修理有限公司 | High-temperature resistant coating |
| MX2021007491A (en) | 2018-12-19 | 2021-08-05 | Ppg Ind Ohio Inc | Sprayable silicone polymer dispersion. |
| CN113563598B (en) * | 2021-08-04 | 2023-04-07 | 宁波锋成先进能源材料研究院有限公司 | Amphiphilic hyperbranched polymer and preparation method and application thereof |
| CN116285657A (en) * | 2021-12-06 | 2023-06-23 | 中国石油化工股份有限公司 | High-resistance and thermal-resistance gas gel coating and preparation method thereof |
| CN118006291B (en) * | 2024-04-10 | 2024-07-02 | 临朐县金迪胶业有限公司 | Moisture-heat resistant silicone structural adhesive suitable for photovoltaic module |
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| JP2005139343A (en) * | 2003-11-07 | 2005-06-02 | Nippon Yushi Basf Coatings Kk | Thermosetting coating material composition, method for coating finishing and coated article |
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| JP2005139343A (en) * | 2003-11-07 | 2005-06-02 | Nippon Yushi Basf Coatings Kk | Thermosetting coating material composition, method for coating finishing and coated article |
| CN101707934A (en) * | 2007-03-19 | 2010-05-12 | 迈图高新材料有限责任公司 | Novel polyamide-polysiloxane compounds |
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