CN105969119A - Environmental friendly furniture coating and preparation method thereof - Google Patents

Environmental friendly furniture coating and preparation method thereof Download PDF

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Publication number
CN105969119A
CN105969119A CN201610187078.8A CN201610187078A CN105969119A CN 105969119 A CN105969119 A CN 105969119A CN 201610187078 A CN201610187078 A CN 201610187078A CN 105969119 A CN105969119 A CN 105969119A
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刘辉
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/06Unsaturated polyesters having carbon-to-carbon unsaturation
    • 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

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Paints Or Removers (AREA)

Abstract

The invention discloses an environmental friendly furniture coating, which is composed of the following raw materials (by weight): 3-4 parts of beeswax, 1-1.6 parts of alkenyl succinic anhydride, 10-12 parts of tung oil, 0.06-0.07 part of sodium hydroxide, 3-4 parts of methanol, 0.1-0.2 part of perfluorosulfonate resin, 6-8 parts of acetic acid, 10-15 parts of 26-30% hydrogen peroxide, 10-17 parts of tetraethyl orthosilicate, 0.1-0.2 part of Y-chloropropyltrimethoxysilane, 70-80 parts of unsaturated polyester resin, 0.6-1 part of methylethyl ketone peroxide, 10-14 parts of vermiculite powder, 2-3 parts of calcium aluminate, 0.7-1 part of hydrogenated castor oil, 1-2 parts of polylactic acid, 0.8-2 parts of dimethylpropane carboxylate and 0.1-0.3 part of dimethyl formamide. The raw materials are environmental friendly, and no poisonous and harmful components are volatilized. As a furniture coating, the product will not harm the health of human body.

Description

A kind of environmental protection coatings for furniture and preparation method thereof
Technical field
The present invention relates to coatings for furniture technical field, particularly relate to a kind of environmental protection coatings for furniture and preparation method thereof.
Background technology
Saturated polyester resin is to prepare one of conventional film-forming resin of coating, but use unsaturated polyester resins for general purpose to there is the shortcomings such as resistance to water, solvent resistance, thermostability and poor mechanical property when preparing coating, need unsaturated polyester resin is modified to improve its combination property and currently mainly utilize polyurethane or base polyurethane prepolymer for use as, acrylic resin, epoxy resin, organosilicon, nano material and vegetable oil etc. unsaturated polyester resin to be modified to improving performance when it prepares coating.Wherein, plant oil modified unsaturated polyester vinegar resin is increasingly paid attention to by people.Vegetable oil is incorporated in unsaturated polyester resin by chemical reaction, easily cause the polyreaction of vegetable oil self, make the limited vegetable oil of modified effect also due to both poor compatibility, modification can be caused by the method modified unsaturated polyester resin being blended to fall flat.Therefore, after vegetable oil derivatization, improve the compatibility of vegetable oil and unsaturated polyester resin, be the important channel of plant oil modified unsaturated polyester resin.
In crude vegetal, Oleum Verniciae fordii is more special, and its main component is eleostearic acid glyceride, has conjugated triene structures, can be used alone in oil-based paint, it is also possible to neutralize other semi-drying oils at synthetic resin coating, non-drying oil is used in mixed way.Oleum Verniciae fordii also has good water proofing property, is widely used in building, paints, prints aspects such as (ink).
Summary of the invention
The object of the invention is contemplated to make up the defect of prior art, it is provided that a kind of environmental protection coatings for furniture and preparation method thereof.
The present invention is achieved by the following technical solutions:
A kind of environmental protection coatings for furniture, it is made up of the raw material of following weight parts:
Cera Flava 3-4, alkenyl succinic anhydride 1-1.6, Oleum Verniciae fordii 10-12, sodium hydroxide 0.06-0.07, methanol 3-4, perfluorinated sulfonic resin 0.1-0.2, acetic acid 6-8, the hydrogen peroxide 10-15 of 26-30%, tetraethyl orthosilicate 10-17, Y-r-chloropropyl trimethoxyl silane 0.1-0.2, unsaturated polyester resin 70-80, methyl ethyl ketone peroxide 0.6-1, vermiculite power 10-14, calcium aluminate 2-3, castor oil hydrogenated 0.7-1, polylactic acid 1-2, dimethylpropane carboxylate 0.8-2, dimethylformamide 0.1-0.3.
The preparation method of a kind of described environmental protection coatings for furniture, comprises the following steps:
(1) joining in Oleum Verniciae fordii by above-mentioned methanol, add sodium hydroxide, react 70-80 minute at 37-40 DEG C under stirring condition, distill methanol removal, stratification, the supernatant liquid of collection first with sulfuric acid scrubbing, the washing of reusable heat water, distillation dehydration, obtains methyl eleostearate;
(2) 50-60% of above-mentioned methyl eleostearate, perfluorinated sulfonic resin, above-mentioned acetic acid weight is mixed, rise high-temperature and be 60-68 DEG C, the hydrogen peroxide of above-mentioned 26-30% is dripped under stirring condition, insulation reaction 3-4 hour after dropping, filter, filtrate is neutralized with alkali, washing, it is vacuum dried 3-4 hour at 50-60 DEG C, obtains epoxidation methyl eleostearate;
(3) above-mentioned alkenyl succinic anhydride is joined in the deionized water of its weight 8-10 times, stir, add dimethylformamide, at 50-60 DEG C, be incubated 3-5 minute, obtain anhydride solution;
(4) by above-mentioned castor oil hydrogenated, Cera Flava mixing, stir, send in the water bath with thermostatic control of 70-80 DEG C, insulated and stirred 10-15 minute, discharging, add dimethylpropane carboxylate, stirring is to room temperature, mixing with above-mentioned epoxidation methyl eleostearate, 70-100 rev/min is stirred 10-15 minute, for premix methyl ester;
(5) by above-mentioned tetraethyl orthosilicate, premix methyl ester mixing, warming temperature is 36-40 DEG C, add remaining acetic acid, polylactic acid, insulated and stirred 10-20 minute, drips the deionized water of above-mentioned mixed system weight 40-50%, adds Y-r-chloropropyl trimethoxyl silane after dropping, it is incubated 6-7 hour at 76-80 DEG C, add above-mentioned anhydride solution, continue insulated and stirred 20-30 minute, obtain silica sol modified epoxidation methyl eleostearate;
(6) above-mentioned silica sol modified epoxidation methyl eleostearate is mixed with remaining each raw material, melt extruded by extruder, after then tabletting is broken, then through pulverizing, sieving, to obtain final product.
The invention have the advantage that
The epoxidation methyl eleostearate molecular structure of the present invention contains epoxy bond and double bond simultaneously, with the carboxyl in unsaturated polyester resin, hydroxyl and double bond, oxidation cross-linked reaction can occur, improve the crosslink density of film, improve filming performance, thus improve the hot strength of film, also improve hardness and the shock resistance of film to a certain extent simultaneously;
Containing hydrophobic fatty acid Long carbon chain in the epoxidation methyl eleostearate of the present invention, when Oleum Verniciae fordii derivant is dispersed in film forming in unsaturated polyester resin, these hydrophobic aliphatic hydrocarbyl groups are at film surface enrichment, film is made to be in a kind of low-surface-energy state, reduce the combination energy on surface and hydrone, thus reduce the water absorption rate of unsaturated polyester resin film, improve unsaturated polyester resin water resistance;
The epoxidation methyl eleostearate of the present invention contains conjugated double bond, and conjugated double bond, in the film forming later stage, occurs oxidation cross-linked, forming network polymers, so that it is tightr to be combined with each other between molecule, the density of film increases, solvent molecule slows down at the permeating speed of film coated surface, thus solvent resistance strengthens;
The epoxidation methyl eleostearate of the present invention has aliphatic long-chain hydrocarbon, and long chain hydrocarbon can play the effect of plasticising in resin, it is possible to strengthen the flexility of unsaturated polyester resin;
The raw material environmental protection of the present invention, volatilizees without poisonous and harmful element, as coatings for furniture, will not be detrimental to health.
Detailed description of the invention
A kind of environmental protection coatings for furniture, it is made up of the raw material of following weight parts:
Cera Flava 3, alkenyl succinic anhydride 1, Oleum Verniciae fordii 10, sodium hydroxide 0.06, methanol 3, perfluorinated sulfonic resin 0.1, the hydrogen peroxide 10 of acetic acid 6,26%, tetraethyl orthosilicate 10, Y r-chloropropyl trimethoxyl silane 0.1, unsaturated polyester resin 70, methyl ethyl ketone peroxide 0.6, vermiculite power 10, calcium aluminate 2, castor oil hydrogenated 0.7, polylactic acid 1, dimethylpropane carboxylate 0.8, dimethylformamide 0.1.
The preparation method of a kind of described environmental protection coatings for furniture, comprises the following steps:
(1) joining in Oleum Verniciae fordii by above-mentioned methanol, add sodium hydroxide, react 70 minutes at 37 DEG C under stirring condition, distill methanol removal, stratification, the supernatant liquid of collection first with sulfuric acid scrubbing, the washing of reusable heat water, distillation dehydration, obtains methyl eleostearate;
(2) by above-mentioned methyl eleostearate, perfluorinated sulfonic resin, 50% mixing of above-mentioned acetic acid weight, rising high-temperature is 60 DEG C, the hydrogen peroxide of above-mentioned 26% is dripped under stirring condition, insulation reaction 3 hours after dropping, filter, filtrate is neutralized with alkali, washing, it is vacuum dried 3 hours at 50 DEG C, obtains epoxidation methyl eleostearate;
(3) above-mentioned alkenyl succinic anhydride is joined in the deionized water of its weight 8 times, stir, add dimethylformamide, at 50 DEG C, be incubated 3 minutes, obtain anhydride solution;
(4) by above-mentioned castor oil hydrogenated, Cera Flava mixing, stir, send in the water bath with thermostatic control of 70 DEG C, insulated and stirred 10 minutes, discharging, adds dimethylpropane carboxylate, and stirring is to room temperature, mixing with above-mentioned epoxidation methyl eleostearate, 70 revs/min are stirred 10 minutes, for premix methyl ester;
(5) by above-mentioned tetraethyl orthosilicate, premix methyl ester mixing, warming temperature is 36 DEG C, add remaining acetic acid, polylactic acid, insulated and stirred 10 minutes, drips the deionized water of above-mentioned mixed system weight 40%, adds Y r-chloropropyl trimethoxyl silane after dropping, it is incubated 6 hours at 76 DEG C, add above-mentioned anhydride solution, continue insulated and stirred 20 minutes, obtain silica sol modified epoxidation methyl eleostearate;
(6) above-mentioned silica sol modified epoxidation methyl eleostearate is mixed with remaining each raw material, melt extruded by extruder, after then tabletting is broken, then through pulverizing, sieving, to obtain final product.
Performance test:
Impact resistance: >=50kg/cm;
Hardness: 2H.

Claims (2)

1. an environmental protection coatings for furniture, it is characterised in that it is made up of the raw material of following weight parts:
Cera Flava 3-4, alkenyl succinic anhydride 1-1.6, Oleum Verniciae fordii 10-12, sodium hydroxide 0.06-0.07, methanol 3-4, perfluorinated sulfonic resin 0.1-0.2, acetic acid 6-8, the hydrogen peroxide 10-15 of 26-30%, tetraethyl orthosilicate 10-17, Y-r-chloropropyl trimethoxyl silane 0.1-0.2, unsaturated polyester resin 70-80, methyl ethyl ketone peroxide 0.6-1, vermiculite power 10-14, calcium aluminate 2-3, castor oil hydrogenated 0.7-1, polylactic acid 1-2, dimethylpropane carboxylate 0.8-2, dimethylformamide 0.1-0.3.
2. the preparation method of an environmental protection coatings for furniture as claimed in claim 1, it is characterised in that comprise the following steps:
(1) joining in Oleum Verniciae fordii by above-mentioned methanol, add sodium hydroxide, react 70-80 minute at 37-40 DEG C under stirring condition, distill methanol removal, stratification, the supernatant liquid of collection first with sulfuric acid scrubbing, the washing of reusable heat water, distillation dehydration, obtains methyl eleostearate;
(2) 50-60% of above-mentioned methyl eleostearate, perfluorinated sulfonic resin, above-mentioned acetic acid weight is mixed, rise high-temperature and be 60-68 DEG C, the hydrogen peroxide of above-mentioned 26-30% is dripped under stirring condition, insulation reaction 3-4 hour after dropping, filter, filtrate is neutralized with alkali, washing, it is vacuum dried 3-4 hour at 50-60 DEG C, obtains epoxidation methyl eleostearate;
(3) above-mentioned alkenyl succinic anhydride is joined in the deionized water of its weight 8-10 times, stir, add dimethylformamide, at 50-60 DEG C, be incubated 3-5 minute, obtain anhydride solution;
(4) by above-mentioned castor oil hydrogenated, Cera Flava mixing, stir, send in the water bath with thermostatic control of 70-80 DEG C, insulated and stirred 10-15 minute, discharging, add dimethylpropane carboxylate, stirring is to room temperature, mixing with above-mentioned epoxidation methyl eleostearate, 70-100 rev/min is stirred 10-15 minute, for premix methyl ester;
(5) by above-mentioned tetraethyl orthosilicate, premix methyl ester mixing, warming temperature is 36-40 DEG C, add remaining acetic acid, polylactic acid, insulated and stirred 10-20 minute, drips the deionized water of above-mentioned mixed system weight 40-50%, adds Y-r-chloropropyl trimethoxyl silane after dropping, it is incubated 6-7 hour at 76-80 DEG C, add above-mentioned anhydride solution, continue insulated and stirred 20-30 minute, obtain silica sol modified epoxidation methyl eleostearate;
(6) above-mentioned silica sol modified epoxidation methyl eleostearate is mixed with remaining each raw material, melt extruded by extruder, after then tabletting is broken, then through pulverizing, sieving, to obtain final product.
CN201610187078.8A 2016-03-28 2016-03-28 Environmental friendly furniture coating and preparation method thereof Withdrawn CN105969119A (en)

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Application Number Priority Date Filing Date Title
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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102993921A (en) * 2012-10-24 2013-03-27 宿迁市英杰装饰材料有限公司 Powder coating with low-temperature curing function
CN103601703A (en) * 2013-07-11 2014-02-26 中南林业科技大学 Method for preparing epoxy methyl eleostearate from tung oil
CN103881341A (en) * 2014-04-04 2014-06-25 中南林业科技大学 Tung oil derivative-modified unsaturated polyester resin composition and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102993921A (en) * 2012-10-24 2013-03-27 宿迁市英杰装饰材料有限公司 Powder coating with low-temperature curing function
CN103601703A (en) * 2013-07-11 2014-02-26 中南林业科技大学 Method for preparing epoxy methyl eleostearate from tung oil
CN103881341A (en) * 2014-04-04 2014-06-25 中南林业科技大学 Tung oil derivative-modified unsaturated polyester resin composition and preparation method thereof

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Application publication date: 20160928