JPH0436358A - Resin composition - Google Patents
Resin compositionInfo
- Publication number
- JPH0436358A JPH0436358A JP2141276A JP14127690A JPH0436358A JP H0436358 A JPH0436358 A JP H0436358A JP 2141276 A JP2141276 A JP 2141276A JP 14127690 A JP14127690 A JP 14127690A JP H0436358 A JPH0436358 A JP H0436358A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- emulsion
- resin composition
- wood
- blowing agent
- 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.)
- Granted
Links
- 239000011342 resin composition Substances 0.000 title claims abstract description 27
- 239000000839 emulsion Substances 0.000 claims abstract description 42
- 229920005989 resin Polymers 0.000 claims abstract description 41
- 239000011347 resin Substances 0.000 claims abstract description 41
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 14
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 14
- 239000004604 Blowing Agent Substances 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 11
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 6
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 4
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000004088 foaming agent Substances 0.000 claims description 12
- 239000003973 paint Substances 0.000 claims description 6
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 3
- 239000002174 Styrene-butadiene Substances 0.000 claims description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
- 239000011115 styrene butadiene Substances 0.000 claims description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 2
- 150000003868 ammonium compounds Chemical class 0.000 claims 1
- 239000011120 plywood Substances 0.000 abstract description 15
- 239000002023 wood Substances 0.000 abstract description 11
- 239000001099 ammonium carbonate Substances 0.000 abstract description 3
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 abstract description 2
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 abstract description 2
- 235000012538 ammonium bicarbonate Nutrition 0.000 abstract description 2
- VQBIMXHWYSRDLF-UHFFFAOYSA-M sodium;azane;hydrogen carbonate Chemical compound [NH4+].[Na+].[O-]C([O-])=O VQBIMXHWYSRDLF-UHFFFAOYSA-M 0.000 abstract 1
- 239000006260 foam Substances 0.000 description 16
- 238000005187 foaming Methods 0.000 description 15
- 238000000576 coating method Methods 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 10
- 239000002518 antifoaming agent Substances 0.000 description 6
- 229920006026 co-polymeric resin Polymers 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- -1 vinyl styrene acetate-butadiene Chemical compound 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 230000002950 deficient Effects 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229920006243 acrylic copolymer Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 description 1
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 206010062717 Increased upper airway secretion Diseases 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- JJLKTTCRRLHVGL-UHFFFAOYSA-L [acetyloxy(dibutyl)stannyl] acetate Chemical compound CC([O-])=O.CC([O-])=O.CCCC[Sn+2]CCCC JJLKTTCRRLHVGL-UHFFFAOYSA-L 0.000 description 1
- CQQXCSFSYHAZOO-UHFFFAOYSA-L [acetyloxy(dioctyl)stannyl] acetate Chemical compound CCCCCCCC[Sn](OC(C)=O)(OC(C)=O)CCCCCCCC CQQXCSFSYHAZOO-UHFFFAOYSA-L 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- PROZFBRPPCAADD-UHFFFAOYSA-N ethenyl but-3-enoate Chemical compound C=CCC(=O)OC=C PROZFBRPPCAADD-UHFFFAOYSA-N 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- SHZIWNPUGXLXDT-UHFFFAOYSA-N ethyl hexanoate Chemical compound CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 125000005474 octanoate group Chemical group 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 208000026435 phlegm Diseases 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyurethanes Or Polyureas (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、気泡含有塗膜を得ることで体積収縮のない、
平滑面を得るための木質用樹脂組成物に関するものであ
る。[Detailed Description of the Invention] [Industrial Field of Application] The present invention provides a coating film containing bubbles that is free from volumetric shrinkage.
The present invention relates to a wood resin composition for obtaining a smooth surface.
〔従来の技術と発明が解決しようとする課題〕従来の木
質用樹脂組成物は、溶剤系と水系に分類され、前者は速
乾性という特徴があるものの有機溶剤を含有、あるいは
用いるために作業者の環境及び健康上の不都合があり、
かつ施工の際は火気に対する危険性の問題がある。後者
は、作業者の健康上に不都合や火気に対する危険性はな
いものの、塗布後の乾燥性が遅く、作業性に問題がある
。[Prior art and problems to be solved by the invention] Conventional wood resin compositions are classified into solvent-based and water-based.The former has the characteristic of quick drying, but contains organic solvents or is difficult to use due to the use of organic solvents. environmental and health disadvantages,
There is also the issue of fire hazard during construction. Although the latter is not inconvenient for the health of workers or poses a risk of fire, it dries slowly after application and has problems with workability.
更に、両者共に塗布後に通常「目ヤセ」と呼ばれる樹脂
の体積収縮によるへこみがでる為、この解決策としてウ
レタン発泡やフェノール発泡などの発泡剤を主体とした
樹脂組成物が上布されている。しかし此等は、近年低級
化する合板やパーティクルボード等の原料である原木に
対応すべく「目ヤセ」のない表面平滑性に秀れた樹脂の
ニズが高くなってきている。しかし、現況下では、塗装
用の通常の汎用機器を使用して気泡含有樹脂を低温で施
工し得る汎用性の良い樹脂組成物を得ることができない
。Furthermore, after both coatings are applied, dents usually occur due to volumetric shrinkage of the resin, which is called "eye loss," so as a solution to this problem, a resin composition based on a foaming agent such as urethane foam or phenol foam is overlaid. However, in recent years, there has been a growing need for resins with excellent surface smoothness without ``eye discoloration'' to cope with the use of raw wood, which is the raw material for plywood, particle board, etc., which has become lower grade in recent years. However, under the current circumstances, it is not possible to obtain a resin composition with good versatility that can be applied with a cell-containing resin at a low temperature using ordinary general-purpose painting equipment.
例えば、最近では、水系エラストマーにポリイソシアネ
ートを添加し、二液混合機械を用いて樹脂組成物として
、合板全表面に塗付し一担平滑に仕上げてから100°
C前後で約10分加温し、発泡硬化せしめ合板表面のへ
こみ、割れ等の欠点を該樹脂組成物で充填した後、余分
の発泡部をペーパーサンディングする事で平滑性を得る
方法が考えられている。しかしこの方法では、100℃
前後の高温下におかれている合板などの木質系材料は「
ネジレ」や「反り」が発生する為に商品としての価値を
損なう場合が多い。For example, recently, polyisocyanate has been added to water-based elastomer, and a resin composition is applied to the entire surface of the plywood using a two-component mixing machine.
One possible method is to heat the plywood for about 10 minutes before and after C to harden the foam, fill in defects such as dents and cracks on the plywood surface with the resin composition, and then sand the excess foam with paper to obtain smoothness. ing. However, with this method, 100℃
Wood-based materials such as plywood that are exposed to high temperatures before and after
The value of the product is often lost due to twisting and warping.
そこでポリイソシアネートを低温で発泡、硬化させる為
に一般に硬化促進助剤があるが、60゛c以下で十分な
硬化発泡を促かす事ができないという問題点があった。Therefore, curing accelerators are generally used to foam and harden polyisocyanate at low temperatures, but there is a problem in that sufficient curing and foaming cannot be promoted at temperatures below 60°C.
ポリイソシアネートを添加する事で常温に於いても発泡
効果は認められるが、数時間を要し、工業的に利用する
には経済的ではなく、又塗膜自体も硬化不充分で後工程
でのサイデイング時にペーパーの「目詰り」を起こす等
の問題があって実用的でない。By adding polyisocyanate, a foaming effect can be observed even at room temperature, but it takes several hours and is not economical for industrial use, and the coating film itself is not sufficiently cured, causing problems in subsequent processes. It is not practical because it causes problems such as paper clogging during siding.
本発明者等は、これらの課題を解決するために、低温で
発泡、硬化し、「ネジレ」 「反り」及び「目ヤセ」の
ない平滑面が得られ、作業性及び生産性の良い、しかも
低コストの木質用樹脂組成物を見出し、本発明を完成し
た。In order to solve these problems, the present inventors have developed a material that foams and hardens at low temperatures, provides a smooth surface without "twisting,""warping," and "fading," and has good workability and productivity. We have discovered a low-cost wood resin composition and completed the present invention.
即ち、水系エマルジョン樹脂に、発泡剤を含有し、又は
、水系エマルジョン樹脂に、発泡剤とポリイソシアネー
ト化合物を含有してなることを特徴とする樹脂組成物に
関する。That is, it relates to a resin composition characterized by containing a blowing agent in an aqueous emulsion resin, or a blowing agent and a polyisocyanate compound in an aqueous emulsion resin.
以下、本発明の詳細な説明する。 The present invention will be explained in detail below.
本発明に使用する水系エマルジョン樹脂の水系エマルジ
ョンは、アクリル系樹脂エマルジョン、酢酸ビニル系樹
脂エマルジョン、塩化ビニル系樹脂エマルジョン、塩化
ビニリデン系樹脂エマルジョンおよびスチレン−ブタジ
エン系樹脂エマルジョンのいずれか1種又は2種以上の
混合物が主に用いられる。The aqueous emulsion of the aqueous emulsion resin used in the present invention is one or two of the following: acrylic resin emulsion, vinyl acetate resin emulsion, vinyl chloride resin emulsion, vinylidene chloride resin emulsion, and styrene-butadiene resin emulsion. A mixture of the above is mainly used.
即ち、水系エマルジョン樹脂としては、ビヒクルにエマ
ルジョン型のアクリル樹脂、酢酸ヒニル系樹脂、塩化ビ
ニリデン樹脂、塩化ビニル−アクリル共重合樹脂、塩化
ビニリデン−アクリル共重合樹脂、アクリル−酢酸ビニ
ル共重合樹脂、塩化ビニル−酢酸ビニル共重合樹脂、酢
酸ビニル共重合樹脂、酢酸ビニルーベオバースチレンー
アクリル共重合樹脂、酢酸ビニルスチレン・ブタジェン
共重合樹脂などを1種あるいは2種以上混合したものが
使用される。That is, the water-based emulsion resin includes an emulsion type acrylic resin, a vinyl acetate resin, a vinylidene chloride resin, a vinyl chloride-acrylic copolymer resin, a vinylidene chloride-acrylic copolymer resin, an acrylic-vinyl acetate copolymer resin, and a chloride resin as a vehicle. One type or a mixture of two or more of vinyl-vinyl acetate copolymer resins, vinyl acetate copolymer resins, vinyl acetate rubeover styrene-acrylic copolymer resins, vinyl styrene acetate-butadiene copolymer resins, etc. are used.
これらに用いられる発泡剤は、炭酸ナトリウム、炭酸水
素ナトリウム、炭酸カルシウム、炭酸マグネシウム、炭
酸アンモニウム、重炭酸アンモニウムなどの炭酸化合物
や塩化アンモニウム、硫酸アンモニウム、硝酸アンモニ
ウムなどのアンモニウム塩が使用される。As blowing agents used for these, carbonate compounds such as sodium carbonate, sodium hydrogen carbonate, calcium carbonate, magnesium carbonate, ammonium carbonate, and ammonium bicarbonate, and ammonium salts such as ammonium chloride, ammonium sulfate, and ammonium nitrate are used.
発泡剤の添加量は、水系エマルジョン塗料のビヒクリに
対して、1〜30重量%(以下、特記しない限り重量%
は、単に%と記す)添加するのが好ましい、添加量が1
%未満では、発泡剤として十分な成果が得られない、ま
た、30%を越えると均一な発泡が得られず好ましくな
い。The amount of the blowing agent added is 1 to 30% by weight based on the vehicle of the water-based emulsion paint (hereinafter, % by weight unless otherwise specified).
is simply written as %) is preferably added, the amount added is 1
If it is less than 30%, sufficient results cannot be obtained as a foaming agent, and if it exceeds 30%, uniform foaming cannot be obtained, which is not preferable.
発泡助剤として用いられるものは、有機スズ化合物が挙
げられる0例えば、スズ(n)アセテート、スズ(If
)オクトエート、スズ(If)エチルヘキソエート、ス
ズ(It)ラウエートのようなカルボン酸塩、ジブチル
スズアセテート、ジブチルスズラウレート、ジブチルス
ズマレエート及びジオクチルスズジアセテートのような
ジアルキルスズ塩が用いられる。Examples of foaming aids used include organic tin compounds. For example, tin (n) acetate, tin (If
) octoate, tin(If) ethylhexoate, carboxylic acid salts such as tin(It) lauate, dialkyltin salts such as dibutyltin acetate, dibutyltin laurate, dibutyltin maleate and dioctyltin diacetate.
添加量としては、通常水系エマルジョン塗料のビヒクル
に対して0.1〜1.0%添加するのが好ましい。The amount added is preferably 0.1 to 1.0% based on the vehicle of the water-based emulsion paint.
また、第三級脂肪族アミンも通常用いられるものであり
、例えばトリエチレンジアミン、N−エチルモルホリン
、N、N、N−テトラメチル−1、3−ブタンジアミン
、ビス−2−(N、N−ジメチルアミノ)エチルエーテ
ル、ジエチレントリアミン、オキシビス(N、N−ジェ
タノールアミン)のような化合物が用いられる。Tertiary aliphatic amines are also commonly used, such as triethylenediamine, N-ethylmorpholine, N,N,N-tetramethyl-1,3-butanediamine, bis-2-(N,N- Compounds such as dimethylamino)ethyl ether, diethylenetriamine, oxybis(N,N-jetanolamine) are used.
該化合物の添加量は、通常水系エマルジョン塗料のビヒ
クルに対して0.1〜0.6%添加するが、好ましくは
0.2〜0.4%である。The amount of the compound added is usually 0.1 to 0.6%, preferably 0.2 to 0.4%, based on the vehicle of the water-based emulsion paint.
発泡剤及び発泡助剤は上記から選ばれる1種及び2種以
上で、単独もしくは混合物でもかまわない。The foaming agent and foaming aid may be one or more selected from the above, and may be used alone or as a mixture.
発泡を均一に、そしてスムースに行なうために、多くの
場合製泡剤が用いられる。これらの整泡剤としては、シ
リコーン系が主に用いられ、水系エマルジョン樹脂のビ
ヒクルに対して0.05〜3.0%添加し、発泡の泡の
大きさ、発泡量、状態を調整する事が望ましい、整泡剤
は消泡剤と同機能のものであり、水系エマルジョン塗料
には通常、消泡剤が加えられているので、この分の消泡
剤を考慮して整泡剤の使用量を定めることが必要である
。Foaming agents are often used to ensure uniform and smooth foaming. Silicone-based foam stabilizers are mainly used, and are added in an amount of 0.05 to 3.0% to the water-based emulsion resin vehicle to adjust the foam size, foaming amount, and condition. It is desirable that the foam stabilizer has the same function as the antifoaming agent, and antifoaming agents are usually added to water-based emulsion paints. It is necessary to determine the amount.
なお、水系エマルジョン塗料中の消泡剤により塗膜の気
泡状態が充分に整泡される場合には整泡剤は配合しなく
てもよい。Note that if the foam condition of the coating film is sufficiently stabilized by the antifoaming agent in the aqueous emulsion paint, the foaming agent may not be added.
水系エマルジョン樹脂の顔料としては、二酸化チタン、
炭酸カルシウム、マイカ、タルク、フレ、ベントナイト
、との粉、カオリンなどが配合されるがこれに限定され
るものではない。Pigments for water-based emulsion resin include titanium dioxide,
Calcium carbonate, mica, talc, phlegm, bentonite, tomato powder, kaolin, etc. are blended, but are not limited thereto.
なお、水系エマルジョン樹脂にその他使用される添加剤
としては、シックナー、分散剤、造膜助剤などが必要に
より加えられる。In addition, as other additives used in the aqueous emulsion resin, a thickener, a dispersant, a film forming aid, etc. may be added as necessary.
通常、樹脂組成物は塗装置前に調整され、通常の塗布手
段により直ちに塗布される。通常は調整した樹脂組成物
を直ちに塗布すれば良いが水系エマルジョン樹脂と発泡
剤、発泡助剤、製泡剤、消泡剤、分散剤及び顔料が塗装
時に混合されて樹脂組成物となり、ロールやナイフコー
ターなど、通常の塗布手段にて塗布される。Usually, the resin composition is prepared before coating and immediately applied by conventional application means. Normally, the prepared resin composition can be applied immediately, but the water-based emulsion resin, foaming agent, foaming aid, foaming agent, antifoaming agent, dispersing agent, and pigment are mixed during coating to form a resin composition, which can be applied to rolls or It is applied using a conventional coating method such as a knife coater.
水系エマルジョン樹脂に配合された発泡剤が若干加温さ
れた程度で分解し、小さな気泡を発生させ、更に発泡助
剤により、発泡を促進、硬化せしめ気泡を含有した強固
な塗膜を形成する。The foaming agent blended into the water-based emulsion resin decomposes when slightly heated to generate small bubbles, and the foaming aid promotes and hardens the foaming to form a strong coating film containing bubbles.
樹脂組成物に整泡剤あるいは消泡剤が配合されている場
合には、発生する気泡が、更に均一に発泡、調整される
。When a foam stabilizer or an antifoaming agent is blended into the resin composition, the generated bubbles are more uniformly expanded and controlled.
発泡する気泡が均一に発泡、硬化する温度は40〜80
℃が好ましく、更に好ましくは40〜60゛cである。The temperature at which foaming bubbles uniformly foam and harden is 40-80℃.
The temperature is preferably 40-60°C, more preferably 40-60°C.
発泡した塗膜には塗膜全体に気泡が生ずるが、気泡ので
き方、量、成長速度などはエマルジョン樹脂および発泡
剤の種類、量、整泡剤などにより相違するので適宜に配
合処方が定められる。Bubbles are formed throughout the foamed coating film, but the formation, amount, and growth rate of the bubbles vary depending on the type and amount of the emulsion resin and blowing agent, foam stabilizer, etc., so the formulation should be determined accordingly. It will be done.
更に、本発明ではポリイソシアネートを添加することに
より、初期の目標を達成することが可能である。Furthermore, in the present invention it is possible to achieve the initial goal by adding polyisocyanates.
即ち、水系エマルジョン樹脂に発泡剤、発泡助剤、整泡
剤、消泡剤、分散剤及び顔料を添加し、更にポリイソシ
アネート化合物を添加、混合すれば、該発泡剤の効果に
より低温での硬化速度が速くなり、初期の目標を達成す
ることが出来るのである。That is, by adding a foaming agent, a foaming aid, a foam stabilizer, an antifoaming agent, a dispersing agent, and a pigment to an aqueous emulsion resin, and then adding and mixing a polyisocyanate compound, the foaming agent can cure the resin at low temperatures. This will increase your speed and allow you to achieve your initial goals.
ポリイソシアネートの使用形態としては、2.4異性体
と2,6異性体よりなり、2.4異性体が約65乃至8
0%に、及び通常の混合物の1つであればかまわない、
しかし、芳香族環1個当り平均2個のイソシアネート基
を有する他のポリイソシアネートも適当である。The usage form of polyisocyanate is 2.4 isomer and 2,6 isomer, and 2.4 isomer is about 65 to 8
0% and one of the normal mixtures,
However, other polyisocyanates having an average of two isocyanate groups per aromatic ring are also suitable.
このような化合物の例としては、フェニレンジイソシア
ネート、ナフタレンジイソシアネート、キシレンジイソ
シアネート、ジフェニル−4,4“−ジイソシアネート
、ヘキサメチレンジイソシアネート、イソホロンジイソ
シアネート、ビス(イソシアネート)メチルシクロヘキ
サン、トリメチルへキサメチレンジイソシアネートなど
が配合される。Examples of such compounds include phenylene diisocyanate, naphthalene diisocyanate, xylene diisocyanate, diphenyl-4,4"-diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, bis(isocyanate)methylcyclohexane, trimethylhexamethylene diisocyanate, etc. Ru.
これらの添加量は、水系エマルジョン樹脂のビヒクルに
対し、5〜50%添加、混合される。水系エマルジョン
樹脂のビヒクルとしては一般的な樹脂を挙げたが発泡し
た塗膜の用途、必要性能に応して樹脂の組成Tg(ガラ
ス転移点)、分子量、更には量が決定される。These additives are added in an amount of 5 to 50% and mixed with respect to the vehicle of the aqueous emulsion resin. Although common resins are used as vehicles for water-based emulsion resins, the composition Tg (glass transition point), molecular weight, and amount of the resin are determined depending on the use and required performance of the foamed coating film.
また、ポリイソシアネートの種類、量も発泡した塗膜の
用途、必要性能に応じて定められる。Further, the type and amount of polyisocyanate are determined depending on the use and required performance of the foamed coating film.
かくして得られた樹脂組成物は、合板及びパーティクル
ボードのような木質材料に塗布され「目ヤセ」がなく「
ネジレj 「反りJもない被塗布材で平滑に仕上げるこ
とができ、サンディング適性も良好な二次加工用木質材
料として好ましい。The resin composition thus obtained can be applied to wood materials such as plywood and particle board without causing "eye discoloration".
Twisted "It is a coated material that does not warp, can be finished smoothly, and has good sanding suitability, making it suitable as a wood material for secondary processing.
(実施例)
以下、実施例及び比較例によって本発明の詳細な説明す
る。(Examples) Hereinafter, the present invention will be explained in detail with reference to Examples and Comparative Examples.
尚、実施例及び比較例において部は重量基準を表わす。In addition, in Examples and Comparative Examples, parts represent weight standards.
実施例1
まず、水系エマルジョン樹脂として第1表の配合A、B
、C5DOものを用意した。Example 1 First, formulations A and B in Table 1 were used as water-based emulsion resins.
, I prepared a C5DO one.
次いで発泡剤、発泡助剤及びポリイソシアネートとして
第2表の配合■、■、■、■のものを用意した。Next, formulations (1), (2), (2), and (2) shown in Table 2 were prepared as blowing agents, blowing aids, and polyisocyanates.
第1表
第2表
しかして、水系エマルジョン樹脂とポリイソシアネート
の配合物を第3表に示す組合せにより各合計量づつ混合
して樹脂組成物Al〜DIVの16種を得た。As shown in Table 1, 16 types of resin compositions Al to DIV were obtained by mixing the combinations of aqueous emulsion resins and polyisocyanates in the total amounts shown in Table 3.
第3表
樹脂組成物AI−DIVは水系エマルジョン樹脂と発泡
剤配合の混合直後のものを試験用の2.5mm合板(通
常6板と呼ばれる裏板を表にも使用、割れやピンホール
なとの凹部の欠点を有するもの)にナイフコーターにて
2.5−一合板全面に50〜100g/ボ塗布した後、
50〜60℃にて10分間加温し発泡、硬化させ、欠点
凹部を平滑あるいは若干の凸部にならしめた。Table 3 The resin composition AI-DIV was prepared by using a 2.5 mm plywood board for testing (usually a back board called 6 board was also used for the front board, and there were no cracks or pinholes. After applying 50 to 100 g/bo on the entire surface of the 2.5-1 plywood using a knife coater,
It was heated at 50 to 60° C. for 10 minutes to foam and harden, and the defective concave portions were made smooth or slightly convex.
その結果、樹脂組成物を塗布、乾燥した2、5+n+合
板に「ネジレ」 「反り」の発生はなく、また、サンデ
ィングを行なっても、サンディングペーパーの「目詰ま
り」はなかった。As a result, the 2,5+n+ plywood coated with the resin composition and dried did not exhibit any "twisting" or "warping", and even when sanding was performed, the sanding paper was not "clogged".
さらに、サンディングを行なった2、51合板を10日
間室温に放置したが「目ヤセ」はなかった。Furthermore, the sanded 2.51 plywood was left at room temperature for 10 days, but there was no "eye discoloration".
比較例1〜3
水系エマルジョン樹脂組成物100部にポリイソシアネ
ートを5〜15部添加し、必要に応じて発泡助剤を混合
した第4表の配合、1.2.3のものを用意した。Comparative Examples 1 to 3 Formulations 1.2.3 in Table 4 were prepared by adding 5 to 15 parts of polyisocyanate to 100 parts of an aqueous emulsion resin composition, and mixing a foaming aid as needed.
樹脂組成物、比較例1〜3は実施例と同条件にて、発泡
状態を確認したところ、ピンホールなどの欠点凹部を平
滑にするまでの発泡は得られなかった。When the foaming state of the resin compositions and Comparative Examples 1 to 3 was confirmed under the same conditions as in the examples, foaming to the extent of smoothing out defective recesses such as pinholes was not obtained.
そこで乾燥温度を90〜100℃にし、10〜20分間
十分な加熱を行ったところ、該欠点部の発泡、硬化は得
られたものの、平滑面にすべきサンダー仕上げ時のサン
ドペーパーの目詰りを起こし実施例1におけるサンダー
適性性能を比較した結果からも大きく劣るものであった
。Therefore, when we set the drying temperature to 90 to 100 degrees Celsius and heated the area sufficiently for 10 to 20 minutes, we were able to foam and harden the defective area, but it also prevented clogging of the sandpaper during sanding, which is required to create a smooth surface. The results of comparing the sanding suitability performance of Example 1 also showed that it was significantly inferior.
本発明によれば、従来技術では達成されなかった、合板
に塗布後の「目ヤセ」による体積収縮、合板の「ネジレ
」 「反り」、さらには、サンディング時の「目詰まり
」等の発生防止が達成されることが判った。According to the present invention, it is possible to prevent volumetric shrinkage due to "scattering" after coating plywood, "twisting" and "warping" of plywood, and "clogging" during sanding, which could not be achieved with conventional technology. was found to be achieved.
即ち、従来技術ではこれらの現象の目的が達成されず、
本発明では水系エマルシヨンに発泡剤を添加、混合し、
樹脂組成物に特徴をもたせ、乾燥温度が低温であるにも
拘らず、発泡、硬化が均一に行われ、これらの現象が全
て満足している樹脂組成物を得ることができた。That is, the conventional technology does not achieve the purpose of these phenomena;
In the present invention, a blowing agent is added to and mixed with the water-based emulsion,
It was possible to obtain a resin composition that has characteristics, that foams and hardens uniformly despite the low drying temperature, and that satisfies all of these phenomena.
今後益々、原木事情の悪化する木質及び合板業界に与え
る影響は大なるものがあり、本発明の意義は大きい。In the future, the raw wood situation will continue to worsen, which will have a significant impact on the wood and plywood industries, and the present invention is of great significance.
特許出願人 三井東圧化学株式会社 第4表Patent applicant Mitsui Toatsu Chemical Co., Ltd. Table 4
Claims (1)
とを特徴とする樹脂組成物。 2)水系エマルジョン樹脂に、発泡剤とポリイソシアネ
ート化合物を含有してなることを特徴とする樹脂組成物
。 3)水系エマルジョン塗料の水系エマルジョンが、アク
リル系樹脂エマルジョン、酢酸ビニル系樹脂エマルジョ
ン、塩化ビニル系樹脂エマルジョン、塩化ビニリデン系
樹脂エマルジョンおよびスチレン−ブタジエン系樹脂エ
マルジョンのいずれか一種又は二種以上の混合物である
特許請求の範囲第1項又は第2項記載の樹脂組成物。 4)発泡剤が、炭酸化合物、アンモニウム化合物からな
る群より選ばれる特許請求の範囲第1項又は第2項記載
の樹脂組成物。[Scope of Claims] 1) A resin composition characterized by containing a foaming agent in an aqueous emulsion resin. 2) A resin composition comprising a water-based emulsion resin containing a foaming agent and a polyisocyanate compound. 3) The water-based emulsion of the water-based emulsion paint is any one or a mixture of two or more of acrylic resin emulsion, vinyl acetate-based resin emulsion, vinyl chloride-based resin emulsion, vinylidene chloride-based resin emulsion, and styrene-butadiene-based resin emulsion. A resin composition according to claim 1 or 2. 4) The resin composition according to claim 1 or 2, wherein the blowing agent is selected from the group consisting of carbonate compounds and ammonium compounds.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2141276A JPH0798906B2 (en) | 1990-06-01 | 1990-06-01 | Resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2141276A JPH0798906B2 (en) | 1990-06-01 | 1990-06-01 | Resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0436358A true JPH0436358A (en) | 1992-02-06 |
JPH0798906B2 JPH0798906B2 (en) | 1995-10-25 |
Family
ID=15288127
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2141276A Expired - Fee Related JPH0798906B2 (en) | 1990-06-01 | 1990-06-01 | Resin composition |
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Country | Link |
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JP (1) | JPH0798906B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005307592A (en) * | 2004-04-22 | 2005-11-04 | Kubota Matsushitadenko Exterior Works Ltd | Exterior wall material |
JP2006503172A (en) * | 2002-10-11 | 2006-01-26 | ユニバーシティ オブ コネチカット | Blends of amorphous and semi-crystalline polymers with shape memory properties |
JP2019519627A (en) * | 2016-04-29 | 2019-07-11 | ダウ グローバル テクノロジーズ エルエルシー | Multilayer coating and process for preparing the multilayer coating |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58101139A (en) * | 1981-12-10 | 1983-06-16 | Otsuka Chem Co Ltd | Crosslinkable composition of vinyl chloride resin |
JPS6136336A (en) * | 1984-07-30 | 1986-02-21 | Toyo Soda Mfg Co Ltd | Production of powdery rubber |
JPH02110142A (en) * | 1988-10-19 | 1990-04-23 | Suzuki Motor Co Ltd | Expandable composition |
-
1990
- 1990-06-01 JP JP2141276A patent/JPH0798906B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58101139A (en) * | 1981-12-10 | 1983-06-16 | Otsuka Chem Co Ltd | Crosslinkable composition of vinyl chloride resin |
JPS6136336A (en) * | 1984-07-30 | 1986-02-21 | Toyo Soda Mfg Co Ltd | Production of powdery rubber |
JPH02110142A (en) * | 1988-10-19 | 1990-04-23 | Suzuki Motor Co Ltd | Expandable composition |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006503172A (en) * | 2002-10-11 | 2006-01-26 | ユニバーシティ オブ コネチカット | Blends of amorphous and semi-crystalline polymers with shape memory properties |
JP2005307592A (en) * | 2004-04-22 | 2005-11-04 | Kubota Matsushitadenko Exterior Works Ltd | Exterior wall material |
JP4551115B2 (en) * | 2004-04-22 | 2010-09-22 | クボタ松下電工外装株式会社 | Exterior wall material |
JP2019519627A (en) * | 2016-04-29 | 2019-07-11 | ダウ グローバル テクノロジーズ エルエルシー | Multilayer coating and process for preparing the multilayer coating |
Also Published As
Publication number | Publication date |
---|---|
JPH0798906B2 (en) | 1995-10-25 |
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