JPH01165675A - Powder coating material composition - Google Patents
Powder coating material compositionInfo
- Publication number
- JPH01165675A JPH01165675A JP32351287A JP32351287A JPH01165675A JP H01165675 A JPH01165675 A JP H01165675A JP 32351287 A JP32351287 A JP 32351287A JP 32351287 A JP32351287 A JP 32351287A JP H01165675 A JPH01165675 A JP H01165675A
- Authority
- JP
- Japan
- Prior art keywords
- powder coating
- material composition
- coating material
- polyolefin
- coating
- 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
- 239000000843 powder Substances 0.000 title claims abstract description 49
- 239000000203 mixture Substances 0.000 title claims abstract description 12
- 238000000576 coating method Methods 0.000 title abstract description 42
- 239000011248 coating agent Substances 0.000 title abstract description 37
- 239000000463 material Substances 0.000 title abstract description 5
- 229920000098 polyolefin Polymers 0.000 claims abstract description 18
- 239000007787 solid Substances 0.000 claims abstract description 16
- -1 polyethylene Polymers 0.000 claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 239000011347 resin Substances 0.000 claims abstract description 15
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 14
- 239000004698 Polyethylene Substances 0.000 claims abstract description 8
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 8
- 229920000573 polyethylene Polymers 0.000 claims abstract description 8
- 238000009503 electrostatic coating Methods 0.000 claims abstract description 6
- 239000004743 Polypropylene Substances 0.000 claims abstract 2
- 229920001155 polypropylene Polymers 0.000 claims abstract 2
- 239000008199 coating composition Substances 0.000 claims description 7
- 238000002844 melting Methods 0.000 abstract description 5
- 230000008018 melting Effects 0.000 abstract description 5
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 239000003973 paint Substances 0.000 description 11
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- 239000000049 pigment Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- 239000003822 epoxy resin Substances 0.000 description 5
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229920000647 polyepoxide Polymers 0.000 description 5
- 241000951471 Citrus junos Species 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- 239000004408 titanium dioxide Substances 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- YSBPNMOAQMQEHE-UHFFFAOYSA-N (2-methyloxiran-2-yl)methyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1(C)CO1 YSBPNMOAQMQEHE-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- 240000004307 Citrus medica Species 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000004705 High-molecular-weight polyethylene Substances 0.000 description 1
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 239000004844 aliphatic epoxy resin Substances 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 1
- AFEQENGXSMURHA-UHFFFAOYSA-N oxiran-2-ylmethanamine Chemical compound NCC1CO1 AFEQENGXSMURHA-UHFFFAOYSA-N 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- 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、粉体塗料の流動性、摩擦溶融性等を改良した
、塗装作業性に優れた静電塗装用熱硬化型粉体塗料組成
物に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention provides a thermosetting powder coating composition for electrostatic coating that has improved fluidity, friction melting properties, etc., and has excellent coating workability. It is about things.
粉体塗料の塗装方法として静電スプレー塗装法が塗着効
率が良いことから広く採用されている。Electrostatic spray coating is widely used as a powder coating method due to its high coating efficiency.
ところで静電スプレー塗装において、粉体塗料を塗料タ
ンクからスプレーガンに搬送するには、エアーが用いら
れているが、その圧力は相当高く、その結果搬送途中の
粉体塗料は、粉体同志の衝突あるいは装置内部での摩擦
により粉体塗料が一部溶融し、粉体同志が融着したり、
また塗料タンクのエジェクタ一部、塗料ホース内に粉体
塗料がコレステロールとして融着してくるという問題点
があった。By the way, in electrostatic spray painting, air is used to transport the powder paint from the paint tank to the spray gun, but the pressure is quite high, and as a result, the powder paint during transport is Part of the powder coating may melt due to collision or friction inside the device, and the powder may fuse together, or
Furthermore, there was a problem in that powder paint was fused as cholesterol to a part of the ejector of the paint tank and inside the paint hose.
そのため得られる塗膜状態が不良となったり、粉体塗料
の搬送が連続運転していると、しだいに不安定となり、
それ故搬送装置の清掃を頻繁に行なう必要があり、これ
に要する工数は多大なものがあり、塗装作業性が悪かっ
た。As a result, the resulting coating film becomes poor, and if powder coating is continuously transported, it gradually becomes unstable.
Therefore, it is necessary to frequently clean the conveying device, which requires a large number of man-hours, and the painting workability is poor.
このような傾向は熱可塑性粉体塗料に比べて、低分子量
の樹脂を使用する熱硬化型粉体塗料において、特に生じ
易かった。This tendency is particularly likely to occur in thermosetting powder coatings that use low molecular weight resins, compared to thermoplastic powder coatings.
本発明はこのような現状に鑑み、鋭意研究を重ねた結果
、前記問題点を解消した、流動性、耐摩擦溶融性等に優
れた静電塗装用熱硬化型粉体塗料組成物を見出し、本発
明に到ったものである。In view of the current situation, as a result of intensive research, the present invention has discovered a thermosetting powder coating composition for electrostatic coating that solves the above problems and has excellent fluidity, friction melting resistance, etc. This has led to the present invention.
すなわち、本発明は、静電塗装用熱硬化型粉体塗料組成
物において、樹脂及びの硬化剤100重量部に対し、数
平均分子量20.000以下の固形ポリオレフィンを0
.1〜5重量部含有させたことを特徴とする粉体塗料組
成物に関するものである。That is, in the thermosetting powder coating composition for electrostatic coating, the present invention contains 0 solid polyolefin having a number average molecular weight of 20.000 or less per 100 parts by weight of the resin and curing agent.
.. The present invention relates to a powder coating composition characterized in that it contains 1 to 5 parts by weight.
本発明は、熱硬化型粉体塗料に固形ポリオレフィンを溶
融混合させることにより予想外にもスプレーガンへの搬
送中において流動性がよく、また粉体同志の衝突あるい
は装置内部での摩擦によっても粉体が溶融しに<<、そ
の結果、粉体同志の融着や、塗料タンクのエジェクタ一
部、塗料ホース内に粉体塗料が融着しにくくなることを
見出したものである。By melt-mixing a solid polyolefin into a thermosetting powder coating, the present invention unexpectedly has good fluidity during transportation to a spray gun, and also prevents particles from colliding with each other or by friction inside the device. The inventors have discovered that as a result, it becomes difficult for the powder to fuse together, or for the powder paint to fuse to a part of the ejector of the paint tank or inside the paint hose.
これら効果の発現機構は明確ではないが恐らく粉体表面
付近にポリオレフィンが部分的に頭を出し、それが滑り
を良くし、その結果流動性がよくなり、かつ摩擦抵抗が
少なくなるからと考えられる。The mechanism by which these effects occur is not clear, but it is thought that the polyolefin partially protrudes near the powder surface, which improves slippage, resulting in better fluidity and less frictional resistance. .
以下、本発明について、詳述する。The present invention will be explained in detail below.
本発明で使用する熱硬化型粉体塗料は従来から公知の樹
脂、硬化剤、さらに必要に応じて各種顔料、添加剤等を
配合した成分からなるものであり、例えばポリエステル
樹脂系、エポキシ樹脂系、アクリル樹脂系熱硬化型粉体
塗料が代表的なものとして挙げられる。また、その製造
方法としては前記樹脂と硬化剤が架橋反応を起さない程
度の温度にて前記成分の混合物をエクストルーダー、熱
ロール、ニーダ−等にて溶融練合し、冷却後粉砕する方
法が代表的なものとして挙げられるが、これらに限定さ
れるものではなく、従来から公知の他の製造方法も採用
出来ることは言うまでもない。The thermosetting powder coating used in the present invention is composed of conventionally known resins, curing agents, and, if necessary, various pigments, additives, etc., such as polyester resins, epoxy resins, etc. A typical example is an acrylic resin thermosetting powder coating. The method for producing it is to melt and knead the mixture of the components using an extruder, hot roll, kneader, etc. at a temperature that does not cause a crosslinking reaction between the resin and the curing agent, and then to crush the mixture after cooling. are mentioned as typical examples, but it goes without saying that the invention is not limited to these, and that other conventionally known manufacturing methods can also be employed.
熱硬化型粉体塗料の構成成分である樹脂としては、ポリ
エステル樹脂、エポキシ樹脂、アクリル樹脂等が代表的
な樹脂として挙げられる。ポリエステル樹脂はテレフタ
ル酸、イソフタル酸、フタル酸、コハク酸、グルタル酸
、アジピン酸、セバシン酸、β−オキシプロピオン酸等
のカルボン酸とエチレングリコール、プロパンジオール
、ブタンジオール、ベンタンジオール、ヘキサンジオー
ル、ネオペンチルグリコール、トリメチロールプロハン
、ペンタエリスリトール等の多価アルコごルとを通常の
方法にて反応させたものが代表的に使用される。Typical resins that are constituent components of thermosetting powder coatings include polyester resins, epoxy resins, acrylic resins, and the like. Polyester resins include carboxylic acids such as terephthalic acid, isophthalic acid, phthalic acid, succinic acid, glutaric acid, adipic acid, sebacic acid, and β-oxypropionic acid, as well as ethylene glycol, propanediol, butanediol, bentanediol, hexanediol, neo Typically used are those obtained by reacting polyhydric alcohols such as pentyl glycol, trimethylolprohane, and pentaerythritol in a conventional manner.
エポキシ樹脂は、分子内に2個以上のエポキシ基ヲ持つ
化合物で、ビスフェノールAとエピクロルヒドリンの縮
合物に代表されるグリシジルエーテル型樹脂、グリシジ
ルエステル型樹脂、グリシジルアミン型樹脂、脂環式エ
ポキシ樹脂、線状脂肪族エポキシ樹脂などが代表的に使
用される。Epoxy resins are compounds with two or more epoxy groups in the molecule, including glycidyl ether type resins such as the condensate of bisphenol A and epichlorohydrin, glycidyl ester type resins, glycidyl amine type resins, alicyclic epoxy resins, Linear aliphatic epoxy resins are typically used.
アクリル樹脂としては、例えばアクリル酸メチル、アク
リル酸エチル、アクリル酸n−ブチル、アクリル酸イソ
ブチル、メタクリル酸メチル、メタクリル酸エチル、メ
タクリル酸n−ブチル、メタクリル酸イソブチル、スチ
レンなどのモノマーとグリシジルアクリレート、グリシ
ジルメタクリレート、2−メチルグリシジルメタクリレ
ートなどのグリシジル基含有モノマーを通常の方法にて
重合させたものが代表的に使用される。Examples of the acrylic resin include monomers such as methyl acrylate, ethyl acrylate, n-butyl acrylate, isobutyl acrylate, methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, and styrene; glycidyl acrylate; Typically used are glycidyl group-containing monomers such as glycidyl methacrylate and 2-methylglycidyl methacrylate, which are polymerized by a conventional method.
熱硬化型粉体塗料の構成成分である硬化剤としては、前
記樹脂の種類により適宜選択されるが、例えばブロック
化ポリイソシアネート、アジピン酸、コハク酸、セバシ
ン酸等の1分子中に2当量以上のカルボキシル基又は酸
無水物を含む化合物、アミノプラスト樹脂、エポキシ樹
脂等が代表的に使用される。The curing agent, which is a component of the thermosetting powder coating, is appropriately selected depending on the type of resin, but for example, 2 equivalents or more per molecule of blocked polyisocyanate, adipic acid, succinic acid, sebacic acid, etc. Compounds containing carboxyl groups or acid anhydrides, aminoplast resins, epoxy resins, etc. are typically used.
顔料としては、二酸化チタン、ベンガラ、酸化鉄、カー
ボンブラック、フタロシアニンブルー、フタロシアニン
グリーン、キナクリドン系顔料、アゾ系顔料、イソイン
ドリノン系顔料などの着色顔料、シリカ、タルク、沈降
性硫酸バリウム、炭酸カルシウムなどの体質顔料が代表
的に使用される。Pigments include coloring pigments such as titanium dioxide, red iron oxide, iron oxide, carbon black, phthalocyanine blue, phthalocyanine green, quinacridone pigments, azo pigments, and isoindolinone pigments, silica, talc, precipitated barium sulfate, and calcium carbonate. Extender pigments such as are typically used.
添加剤としては、垂れ防止剤、表面調整剤、架橋促進触
媒等が使用される。As additives, anti-sag agents, surface conditioners, crosslinking promoting catalysts, etc. are used.
本発明の熱硬化型粉体塗料はこれら成分からなる組成物
を前記溶融練合の際、固形ポリオレフィンを配合し、製
造したものである。The thermosetting powder coating of the present invention is produced by blending a solid polyolefin into a composition made of these components during the melt kneading process.
本発明で使用するポリオレフィンは、ポリエチレン、ポ
リプロピレン、エチレン−プロピレン共重合体あるいは
、これらの混合物が代表的なものとして挙げられる。Typical polyolefins used in the present invention include polyethylene, polypropylene, ethylene-propylene copolymers, and mixtures thereof.
ポリオレフィンは数平均分子量20.000以下、特に
好ましくは乳000以下の常温で固形のポリオレフィン
が使用出来る。ポリオレフィンの分子量が前記範囲より
大き過ぎると、他の樹脂との相溶性が悪くなり、得られ
る塗面がユズ肌等になりやすく、また耐摩擦溶融性の効
果も小さくなるので好ましくない。The polyolefin that can be used is a polyolefin that is solid at room temperature and has a number average molecular weight of 20,000 or less, particularly preferably 000 or less. If the molecular weight of the polyolefin is too large than the above range, the compatibility with other resins will be poor, the resulting coated surface will tend to have a citron skin, and the effect of friction melting resistance will be reduced, which is not preferable.
ポリオレフィンの配合量は、結合剤となる樹脂及びその
硬化剤100重量部に対し、O,1〜5重量部、特に好
ましくは0.3〜3.5重量部が適当である。配合量が
前記範囲より少ないと前記本発明の効果が得られず、逆
に多過ぎると塗面状態に悪影響を及ぼすので好ましくな
い。The appropriate amount of polyolefin to be blended is 1 to 5 parts by weight, particularly preferably 0.3 to 3.5 parts by weight, based on 100 parts by weight of the resin serving as the binder and its curing agent. If the blending amount is less than the above range, the effects of the present invention cannot be obtained, and if it is too large, the coating surface condition will be adversely affected, which is not preferable.
本発明によれば、熱硬化型粉体塗料に固形ポリオレフィ
ンを配合することにより、粉体塗料の流動性、摩擦溶融
性等が改良され、静電塗装作業性のよい、かつ塗面状態
のよい粉体塗料が得られる。According to the present invention, by blending a solid polyolefin into a thermosetting powder coating, the fluidity, friction melting properties, etc. of the powder coating are improved, and the electrostatic coating has good workability and a good coated surface condition. A powder coating is obtained.
以下、本発明を実施例によりさらに詳細に説明する。な
お、実施例中「部」、「%」は重量基準で示す。Hereinafter, the present invention will be explained in more detail with reference to Examples. In the examples, "parts" and "%" are expressed on a weight basis.
注1)「ファインデイックM8000J(大日本インキ
化学工業社製商品名)
注2)rB−1530J (ヒニルス社製商品名)
注3)「エピクロン4050J (大日本インキ化学
工業社製商品名)
注4)表面調整剤と硬化促進剤の(7: 2)からなる
混合物
注5)「サンワックス161−PJ (三洋化成工業
社製商品名;Mn5000)
上記成分をヘンシェルミキサーにて約1分間混合した後
、100〜120℃の温度条件下、押出機(ブスコニー
ダーPR46)で溶融練合し、冷却後、シリカ微粉末を
前記混合成分に0.2%添加し、パンタムミルで粉砕し
たものを200メツシユの金網で篩い、粉体塗料を調製
した。Note 1) FINDIC M8000J (trade name manufactured by Dainippon Ink and Chemicals) Note 2) rB-1530J (trade name manufactured by Hinils) Note 3) Epicron 4050J (trade name manufactured by Dainippon Ink and Chemical) Note 4 ) A mixture consisting of a surface conditioner and a curing accelerator (7:2) Note 5) Sunwax 161-PJ (trade name: Mn5000, manufactured by Sanyo Chemical Industries, Ltd.) After mixing the above components for about 1 minute in a Henschel mixer. , melt-kneaded in an extruder (Busco Kneader PR46) under a temperature condition of 100 to 120°C, and after cooling, 0.2% of silica fine powder was added to the mixed components, and the mixture was ground in a pantum mill, and then mixed into a 200-mesh wire mesh. and sieved to prepare a powder coating.
二酸化チタン 25.7部
フダ口シアニンプル一 〇。3部
注6) rER−6610J (日本エステル社製
商品名)
注7)「フレランUi」 (バイエル社製商品名)
注8)「エピクロン2050J (大日本インキ化学
工業社製商品名)
注9)「ビスコール660−PJ(三洋化成工業社製商
品名;Mn3000)
上記成分から実施例1と同様にして粉体塗料を調製した
。Titanium dioxide 25.7 parts Fudakuchi cyanine 10. 3 copies Note 6) rER-6610J (Product name manufactured by Nippon Ester Co., Ltd.) Note 7) “Fleran Ui” (Product name manufactured by Bayer) Note 8) “Epicron 2050J (Product name manufactured by Dainippon Ink & Chemicals Co., Ltd.) Note 9) "Viscol 660-PJ (trade name, manufactured by Sanyo Chemical Industries, Ltd.; Mn3000) A powder coating was prepared from the above components in the same manner as in Example 1.
沈降性硫酸バリウム 14.7部二酸
化チタン 29.4部黄色酸化鉄
1.0部ベンガラ
0.3 R注10)「エステルレジンER−81
01J(S、本エステル社製商品名)
注目) rエポ)−)YD−014J (東部化成
社製商品名)
注12) 「サン7ツクスLEL−400PJ(三洋
化成工業社製商品名; Mn4000 )上記成分から
実施例1と同様にして粉体塗料を調製した。Precipitated barium sulfate 14.7 parts Titanium dioxide 29.4 parts Yellow iron oxide
1.0 part Red Garla
0.3 R Note 10) “Ester Resin ER-81
01J (S, product name manufactured by Hon-Ester Co., Ltd.) Attention) r Epo) -) YD-014J (product name manufactured by Tobu Kasei Co., Ltd.) Note 12) “Sun7tux LEL-400PJ (product name manufactured by Sanyo Chemical Industries, Ltd.; Mn4000) A powder coating was prepared from the above components in the same manner as in Example 1.
注13)「エステルレジンER−82oo」(日本エス
テル社製商品名)
注14)「エピコー)828 (油化シェル社製商品
名)
上記成分から実施例1と同様にして粉体塗料を調製した
。Note 13) "Ester Resin ER-82oo" (trade name manufactured by Nippon Ester Co., Ltd.) Note 14) "Epicor) 828 (trade name manufactured by Yuka Shell Co., Ltd.) A powder coating was prepared from the above components in the same manner as in Example 1. .
実施例5
実施例4において固形ポリエチレンの配合量を4部とす
る以外は同様にして粉体塗料を調製した。Example 5 A powder coating material was prepared in the same manner as in Example 4 except that the amount of solid polyethylene was changed to 4 parts.
二酸化チタン 54.9部注15)
「ファインデイックA−223SJ(大日本インキ化学
工業社製商品名)
上記成分から実施例1と同様にして粉体塗料を調製した
。Titanium dioxide 54.9 parts Note 15)
"FINDIC A-223SJ (trade name, manufactured by Dainippon Ink & Chemicals) A powder coating was prepared from the above components in the same manner as in Example 1.
比較例1
実施例4において固形ポリエチレンを配合しない以外は
同様にして粉体塗料を調製した。Comparative Example 1 A powder coating was prepared in the same manner as in Example 4 except that solid polyethylene was not blended.
比較例2
実施例4において固形ポリエチレンの配合量を8部とす
る以外は同様にして粉体塗料を調製した。Comparative Example 2 A powder coating was prepared in the same manner as in Example 4 except that the amount of solid polyethylene was changed to 8 parts.
比較例3
実施例4において固形ポリエチレンとしてMn3000
0の高分子量ポリエチレンを使用する以外は同様にして
粉体塗料を調製した。Comparative Example 3 Mn3000 was used as solid polyethylene in Example 4.
A powder coating was prepared in the same manner except that 0 high molecular weight polyethylene was used.
比較例4
実施例6において固形ポリエチレンを配合しない以外は
同様にして粉体塗料を調製した。Comparative Example 4 A powder coating was prepared in the same manner as in Example 6 except that solid polyethylene was not blended.
各実施例、比較例で製造した粉体塗料を、0.8市厚の
磨軟鋼板に静電粉体塗装ガン(ゲマ社製721型)にて
、−60KVの電圧で膜厚60μになるように塗装し、
熱風乾燥炉で焼付けた。The powder coatings produced in each example and comparative example were coated on a polished mild steel plate with a thickness of 0.8 mm using an electrostatic powder coating gun (Model 721 manufactured by Gema Co., Ltd.) at a voltage of -60 KV to a film thickness of 60 μm. Paint it like this,
Baked in a hot air drying oven.
得られた塗膜につき、各種試験を行ない、その結果を第
1表に示す。Various tests were conducted on the resulting coating film, and the results are shown in Table 1.
注16)目視判定
◎:良 好、○:極くわずかユズ肌、
△:ユズ肌、X:ひどいユズ肌
注17) JIS −K −54006,7に準じて6
0°反射率を測定
注18) JIS −Z −22471:準じて判定性
19) JIS −K −54006,13,3に準じ
て、各インチ径、500gのオモリで
測定
注20)粉体塗料を、粉体塗料用ホースと流動タンク内
を45分間!fflさせ、エジェクタ一部への粉体塗料
の融着量を測定
(但し、インジェクターエアーの圧力
5、0 kg/ cut ;流動エアーの圧力0.2
kg/ cut)第1表より明らかの通り、本発明の粉
体塗料は塗膜性能を落さずに、摩擦融着性を格段に改善
することが出来、塗装作業性に優れていた。Note 16) Visual judgment ◎: Good, ○: Very slight yuzu skin, △: Yuzu skin, X: Severe yuzu skin Note 17) 6 according to JIS-K-54006, 7
Measure the 0° reflectance Note 18) JIS-Z-22471: Judgment 19) Measure with each inch diameter and 500 g weight according to JIS-K-54006, 13, 3 Note 20) Powder paint , 45 minutes inside the powder coating hose and fluid tank! ffl, and measure the amount of powder coating fused to a part of the ejector (however, the injector air pressure is 5,0 kg/cut; the fluidizing air pressure is 0.2
kg/cut) As is clear from Table 1, the powder coating of the present invention was able to significantly improve frictional adhesion without deteriorating coating performance, and was excellent in coating workability.
一方、固形ポリオレフィンを配合しない比較例1.4は
摩擦融着性が大きく、また固形ポリオレフィンを過剰に
配合した比較例2は摩擦融着性は改善出来たものの、塗
膜の平滑性、光沢、耐衝撃性等の塗膜性状が低下し、ま
た、固形ポリオレフィンとして分子量の高いものを使用
した比較例3においてば摩擦融着性が左程改善されず、
ひどいユズ肌塗膜となった。On the other hand, Comparative Examples 1 and 4, in which no solid polyolefin was blended, had a high frictional fusion property, and Comparative Example 2, in which an excessive amount of solid polyolefin was blended, had improved friction fusion properties, but the smoothness, gloss, and Coating film properties such as impact resistance deteriorated, and in Comparative Example 3, in which a solid polyolefin with a high molecular weight was used, frictional adhesion was not improved as much.
It resulted in a terrible yuzu skin coating.
Claims (2)
脂及びその硬化剤100重量部に対し、数平均分子量2
0,000以下の固形ポリオレフィンを0.1〜5重量
部含有させたことを特徴とする粉体塗料組成物。(1) In a thermosetting powder coating composition for electrostatic coating, the number average molecular weight is 2 for 100 parts by weight of the resin and its curing agent.
A powder coating composition containing 0.1 to 5 parts by weight of a solid polyolefin having a molecular weight of 0,000 or less.
レンあるいはこれらの混合物であることを特徴とする特
許請求の範囲第(1)項記載の粉体塗料組成物。(2) The powder coating composition according to claim (1), wherein the polyolefin is polyethylene, polypropylene, or a mixture thereof.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62323512A JPH0615676B2 (en) | 1987-12-21 | 1987-12-21 | Powder coating composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62323512A JPH0615676B2 (en) | 1987-12-21 | 1987-12-21 | Powder coating composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01165675A true JPH01165675A (en) | 1989-06-29 |
| JPH0615676B2 JPH0615676B2 (en) | 1994-03-02 |
Family
ID=18155515
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62323512A Expired - Lifetime JPH0615676B2 (en) | 1987-12-21 | 1987-12-21 | Powder coating composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0615676B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01203477A (en) * | 1988-02-08 | 1989-08-16 | Ee B C Shokai:Kk | Solventless coating |
| JP2002528625A (en) * | 1998-10-31 | 2002-09-03 | ビーエーエスエフ コーティングス アクチェンゲゼルシャフト | Powder coatings and their use for producing muffling powder coatings |
| JP2017197762A (en) * | 2011-03-17 | 2017-11-02 | クラリアント・ファイナンス・(ビーブイアイ)・リミテッド | Powder coating composition for structuring and texturing coated surface |
-
1987
- 1987-12-21 JP JP62323512A patent/JPH0615676B2/en not_active Expired - Lifetime
Non-Patent Citations (2)
| Title |
|---|
| PAINT & RESIN=1982 * |
| PAINT MANUFACTURE=1970 * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01203477A (en) * | 1988-02-08 | 1989-08-16 | Ee B C Shokai:Kk | Solventless coating |
| JP2002528625A (en) * | 1998-10-31 | 2002-09-03 | ビーエーエスエフ コーティングス アクチェンゲゼルシャフト | Powder coatings and their use for producing muffling powder coatings |
| JP2017197762A (en) * | 2011-03-17 | 2017-11-02 | クラリアント・ファイナンス・(ビーブイアイ)・リミテッド | Powder coating composition for structuring and texturing coated surface |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0615676B2 (en) | 1994-03-02 |
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