JPS6323975A - Heat-resistant paint composition - Google Patents
Heat-resistant paint compositionInfo
- Publication number
- JPS6323975A JPS6323975A JP16745186A JP16745186A JPS6323975A JP S6323975 A JPS6323975 A JP S6323975A JP 16745186 A JP16745186 A JP 16745186A JP 16745186 A JP16745186 A JP 16745186A JP S6323975 A JPS6323975 A JP S6323975A
- Authority
- JP
- Japan
- Prior art keywords
- polysiloxane
- powder
- modified
- heat
- 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
- 239000000203 mixture Substances 0.000 title abstract description 3
- 239000003973 paint Substances 0.000 title description 8
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 47
- -1 polysiloxane Polymers 0.000 claims abstract description 46
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000010445 mica Substances 0.000 claims abstract description 24
- 229910052618 mica group Inorganic materials 0.000 claims abstract description 24
- 239000000843 powder Substances 0.000 claims abstract description 21
- 239000008199 coating composition Substances 0.000 claims description 13
- 238000000576 coating method Methods 0.000 abstract description 27
- 239000011248 coating agent Substances 0.000 abstract description 26
- 229920005989 resin Polymers 0.000 abstract description 11
- 239000011347 resin Substances 0.000 abstract description 11
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract description 8
- 239000003431 cross linking reagent Substances 0.000 abstract description 5
- 238000002156 mixing Methods 0.000 abstract description 5
- 239000002904 solvent Substances 0.000 abstract description 5
- 125000003545 alkoxy group Chemical group 0.000 abstract description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 4
- 125000005372 silanol group Chemical group 0.000 abstract description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 3
- 239000012298 atmosphere Substances 0.000 abstract description 2
- 125000000524 functional group Chemical group 0.000 abstract description 2
- 239000004593 Epoxy Chemical group 0.000 abstract 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 abstract 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 17
- 229910052782 aluminium Inorganic materials 0.000 description 10
- 229910052742 iron Inorganic materials 0.000 description 8
- 239000000758 substrate Substances 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 6
- 230000002265 prevention Effects 0.000 description 6
- 239000010410 layer Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-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
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 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
- 239000013078 crystal Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 238000010438 heat treatment Methods 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
- 238000000034 method Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen 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
- 239000000049 pigment Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- KDVYCTOWXSLNNI-UHFFFAOYSA-N 4-t-Butylbenzoic acid Chemical compound CC(C)(C)C1=CC=C(C(O)=O)C=C1 KDVYCTOWXSLNNI-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000010960 cold rolled steel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 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 1
- 229910000398 iron phosphate Inorganic materials 0.000 description 1
- WBJZTOZJJYAKHQ-UHFFFAOYSA-K iron(3+) phosphate Chemical compound [Fe+3].[O-]P([O-])([O-])=O WBJZTOZJJYAKHQ-UHFFFAOYSA-K 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
Abstract
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、耐熱性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 relates to a heat-resistant coating composition.
[従来の技術]
排気マフラー、エンジン回り、暖房器、ストーブ、プラ
ント、熱交換器等の鉄素材表面に耐熱性塗料を塗布して
、発錆を防IFすることが従来から行なわれている。[Prior Art] It has been conventional practice to apply a heat-resistant paint to the surface of iron materials such as exhaust mufflers, engine parts, heaters, stoves, plants, heat exchangers, etc. to prevent rusting.
該耐熱性塗料としては、ポリシロキサンにアルミニウム
粉末を含有させた塗料が一般的に使用されている。この
ものは、ポリシロキサン中のシロキサン結合が熱に対し
て安定であること及びアルミニウム粉末が高融点(65
9℃)でそれ自体熱に対し安定な性質を持つことから耐
熱性塗料として有用なものである。As the heat-resistant paint, a paint made of polysiloxane containing aluminum powder is generally used. This material is characterized by the fact that the siloxane bonds in polysiloxane are stable against heat and that the aluminum powder has a high melting point (65
It is useful as a heat-resistant paint because it is stable against heat at a temperature of 9°C.
[発明が解決しようとする問題点]
上記した#熱性塗料から形成される塗膜は、ポリシロキ
サンの分解温度(約250℃)以下では良好な防錆性、
耐熱性を示すものであるが、分解温度より高い温度にさ
らされた場合に、ポリシロキサン自体酸素透過性の大き
な性質を持つため塗膜を透過した酸素が素材の鉄金属と
反応して酸化鉄層を生じ塗膜の付着性を劣化させ塗膜が
剥れるという欠点があるとともに、塗膜がもろくなりわ
ずかの外力で崩壊するという欠点がある。もっとも、こ
の欠点を改良する方法として、前記した耐熱性塗料塗膜
と素材との間に亜鉛粉末を高濃度に含有するポリシロキ
サン塗膜をプライマーとして形成させた2コート塗膜が
考えられるが、#熱性及び防錆性ともに満足できる塗膜
が得られていないのが実情である。[Problems to be Solved by the Invention] The coating film formed from the #thermal paint described above has good rust prevention properties below the decomposition temperature of polysiloxane (approximately 250°C).
It exhibits heat resistance, but when exposed to temperatures higher than its decomposition temperature, as polysiloxane itself has high oxygen permeability, the oxygen that passes through the coating reacts with the iron metal of the material, producing iron oxide. It has the disadvantage that it forms a layer, which deteriorates the adhesion of the coating and causes the coating to peel, and it also has the disadvantage that the coating becomes brittle and collapses under the slightest external force. However, as a method to improve this drawback, a two-coat coating film in which a polysiloxane coating film containing a high concentration of zinc powder is formed as a primer between the heat-resistant paint coating film and the material described above can be considered. #The reality is that a coating film that is satisfactory in both heat resistance and rust prevention properties has not been obtained.
[問題点を解決するための手段]
本発明者は従来の耐熱性塗料組成物のもつ欠点を解決す
べく鋭意研究の結果、変性ポリシロキサンに、リン片状
マイカ粉末及びリン片状アルミニウム粉末を含有した塗
料組成物が高温雰囲気条件下で鉄素地の表面に防錆性に
優れた金属又は非金属との融合被膜層を形成しこのもの
が前記した欠点を解決することを見いだし本発明を完成
するに至った。[Means for Solving the Problems] As a result of intensive research in order to solve the drawbacks of conventional heat-resistant coating compositions, the present inventors added flaky mica powder and flaky aluminum powder to modified polysiloxane. The present invention was completed based on the discovery that the containing coating composition forms a fused coating layer with a metal or non-metal having excellent rust prevention properties on the surface of an iron substrate under high-temperature atmospheric conditions, which solves the above-mentioned drawbacks. I ended up doing it.
即ち、本発明は、変性ポリシロキサン成分100重に部
、長手方向の寸法0.01〜5鉢。That is, in the present invention, the modified polysiloxane component is 100 parts, and the length in the longitudinal direction is 0.01 to 5 pots.
厚さ3000A以下のリン片状マイカ粉末120〜18
0重量部及び長手方向の寸法1〜50pL、比表面J&
1.Om″/g以上のリン片状アルミニウム粉末30〜
70重量部の割合で配合してなる耐熱性塗料組成物に関
する。Scale-like mica powder 120 to 18 with a thickness of 3000A or less
0 parts by weight and longitudinal dimension 1 to 50 pL, specific surface J&
1. Scale-like aluminum powder of Om″/g or more 30~
It relates to a heat-resistant coating composition containing 70 parts by weight.
本発明に用いる変性ポリシロキサンとしては、シラノー
ル基又はアルコキシ基を有するポリシロキサンと水M基
又はカルボキシル基を有する変性樹脂とを縮合して得ら
れる従来公知の変性ポリシロキサンである。このような
変性ポリシロキサンとしては1例えば、ポリエステル変
性ポリシロキサン、アルキド変性ポリシロキサン、アク
リル変性ポリシロキサン、エポキシ変性ポリシロキサン
、メラミン変性ポリシロキサン、フェノール変性ポリシ
ロキサン等が挙げられる。中でも好ましくはポリエステ
ル変性ポリシロキサンである。The modified polysiloxane used in the present invention is a conventionally known modified polysiloxane obtained by condensing a polysiloxane having a silanol group or an alkoxy group with a modified resin having a water M group or a carboxyl group. Examples of such modified polysiloxanes include polyester-modified polysiloxanes, alkyd-modified polysiloxanes, acrylic-modified polysiloxanes, epoxy-modified polysiloxanes, melamine-modified polysiloxanes, and phenol-modified polysiloxanes. Among them, polyester-modified polysiloxane is preferred.
ポリシロキサンとしては、1分子中に1個以上のシラノ
ール基又はアルコキシ基を有するオルガノポリシロキサ
ンが使用される。As the polysiloxane, an organopolysiloxane having one or more silanol groups or alkoxy groups in one molecule is used.
また、変性樹脂としては、上記の樹脂が使用されるがこ
れらの樹脂の原料についてその一例をあげると、例えば
、ポリエステルについては、(無水)フタル酸、イソフ
タル酸、テレフタル醜、アジピン酸、セパチン酸等の多
塩基酸;安息香醜、P−tert−ブチル安息香酸等の
一塩基酸;エチレングリコーμ、ネオペンチルグリコー
μ、1.6−ヘキサンジオーμ、トリメチロールプロパ
ン等の多価アルコール等が挙げられ、アルキド樹脂につ
いては前記ポリエステルの原料以外にアマニ油、サフラ
ワー油、ダイズ油、ヤシ油及びこれらの脂肪酸等を用い
ることができ、アクリル樹脂については、メチル(メタ
)アクリレ−ト、エチル(メタ)アクリレート、ブチル
(メタ)アクリレート、ステアリル(メタ)アクリレー
ト、2−ヒドロキシエチル(メタ)アクリレート、(メ
タ)アクリル酸、 (メタ)アクリルアミド、グ1ノシ
ジル(メタ)アクリレート、スチレン等が挙げられ、エ
ポキシ樹脂については、エピコート828、同1004
、回1007.回1009(以上シェル化学製、商品名
)等のビスフェノールA型が挙げられる。In addition, the above-mentioned resins are used as the modified resin, but to give an example of the raw materials for these resins, for example, for polyester, phthalic acid (anhydride), isophthalic acid, terephthalic acid, adipic acid, and cepatic acid are used. Polybasic acids such as benzoic acid, P-tert-butylbenzoic acid, etc.; Polyhydric alcohols such as ethylene glycol μ, neopentyl glycol μ, 1,6-hexanedioh μ, trimethylolpropane, etc. For alkyd resins, linseed oil, safflower oil, soybean oil, coconut oil, and their fatty acids can be used in addition to the raw materials for polyester, and for acrylic resins, methyl (meth)acrylate, ethyl ( Examples include meth) acrylate, butyl (meth) acrylate, stearyl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, (meth) acrylic acid, (meth) acrylamide, glynosidyl (meth) acrylate, styrene, etc. For epoxy resins, Epicoat 828, Epicoat 1004
, times 1007. Examples include bisphenol A type such as 1009 (manufactured by Shell Chemical Co., Ltd., trade name).
ポリシロキサンと変性樹脂(架橋剤も含む)との配合割
合は、重着比で20/80〜80/20、好ましくは4
0/60〜60/40である。ポリシロキサンの割合が
20より少ないと樹脂中の有機物が分解し始める300
”C以上の高温での膜安定性に劣り、またポリシロキサ
ンの、1合が80より多いと高温時に素地との付着性に
劣る傾向がある。The blending ratio of polysiloxane and modified resin (including crosslinking agent) is 20/80 to 80/20, preferably 4
It is 0/60 to 60/40. If the proportion of polysiloxane is less than 20, the organic matter in the resin will begin to decompose.
The film stability is poor at high temperatures of C or higher, and if the 1 ratio of polysiloxane is more than 80, the adhesion to the substrate tends to be poor at high temperatures.
このような変性ポリシロキサンは、500〜go 、o
oo、好ましくは1,000〜50.000の範囲内の
分子量を有することができる0分子量が500より小さ
い変性ポリシロキサンを用いた場合には造膜性等に劣り
、反対に80.000より大きい分子量をもつ変性ポリ
シロキサンは塗装作業性に劣る傾向がある。Such modified polysiloxanes have 500~go, o
oo, preferably has a molecular weight in the range of 1,000 to 50.000.0 If a modified polysiloxane with a molecular weight of less than 500 is used, film-forming property etc. will be poor, and on the contrary, it will be greater than 80.000. Modified polysiloxanes with high molecular weight tend to have poor coating workability.
上記した変性ポリシロキサンは、シラノール基、アルコ
キシシラン基、水酸基、カルボキシル基、エポキシ基、
アルコキシ基、メチロール基。The modified polysiloxane described above includes a silanol group, an alkoxysilane group, a hydroxyl group, a carboxyl group, an epoxy group,
Alkoxy group, methylol group.
フェノール基及び酸化重合性不飽和二重結合等の官能基
を1種以上有する硬化性の樹脂である。該変性ポリシロ
キサンは単独で又は架橋剤と組合わせて用いることがで
き、架橋剤としては、メラミン樹脂、ポリインシアネー
ト、エポキシ樹脂等が挙げられる。また、架橋剤は変性
樹脂に対して約20〜50重量%の範囲で配合すること
ができる。It is a curable resin having one or more functional groups such as a phenol group and an oxidatively polymerizable unsaturated double bond. The modified polysiloxane can be used alone or in combination with a crosslinking agent, and examples of the crosslinking agent include melamine resin, polyincyanate, and epoxy resin. Further, the crosslinking agent can be blended in an amount of about 20 to 50% by weight based on the modified resin.
本発明に用いるリン片状マイカ粉末としては、長手方向
の寸法0.01〜5W、好ましくは0.1〜3用で厚さ
3000Å以下の範囲内のリン片状の外形をした粉末で
ある。該リン片状マイカ粉末の長手方向の寸法がo、o
tgより小さい場合には高温時の膜安定性に劣り、反対
に5延より大きい場合には造膜性に劣る。またリン片状
マイカ粉末の厚みが3.000人より大きい場合には造
膜性等に劣る。The scale-like mica powder used in the present invention is a powder having a scale-like external shape with a longitudinal dimension of 0.01 to 5W, preferably 0.1 to 3W, and a thickness of 3000 Å or less. The longitudinal dimension of the flaky mica powder is o, o
When it is smaller than tg, the film stability at high temperatures is poor, and on the other hand, when it is larger than 5 g, film forming properties are poor. Furthermore, if the thickness of the scale-like mica powder is greater than 3,000 mm, film-forming properties and the like are poor.
上記したリン片状マイカ粉末として、例えば、マイカS
−100(■山ロ雲母工業所)、マイカA−100(■
山ロ雲母工業所)、マイカA−11(U山ロ雲母工業所
)、マイカA−150(■山ロ雲母工業所)等が挙げら
れる。As the scale-like mica powder described above, for example, mica S
-100 (■ Yamaro Mica Industries), Mica A-100 (■
Examples include Mica A-11 (Yamaro Mica Industries), Mica A-150 (Yamaro Mica Industries), and the like.
また、リン片状マイカ粉末は、一般には結晶水を含有す
るものであるが焼成時により密な塗膜をつくること等の
観点から好ましくは焼成により結晶水を除いたもの、例
えば、マイカS−100を用いることが有利である。In addition, flaky mica powder generally contains crystal water, but from the viewpoint of forming a denser coating film during firing, it is preferable to use mica powder from which crystal water has been removed by firing, such as mica S- It is advantageous to use 100.
リン片状マイカ粉末の配合量は、変性ポリシロキサン固
形分100重に部に対し120〜180屯h:部、好ま
しくは140〜160重量部の範囲内である。該リン片
状マイカ粉末の配合量が120より少ない場合には高温
時の膜安定性等が劣り、反対に180より多い場合には
造膜性等に劣る。The amount of scale-like mica powder blended is within the range of 120 to 180 ton h parts, preferably 140 to 160 parts by weight, per 100 parts by weight of the modified polysiloxane solid content. If the amount of the scale-like mica powder blended is less than 120, film stability at high temperatures is poor, and on the other hand, if it is more than 180, film forming properties are poor.
本発明に用いるリン片状アルミニウム粉末としては、長
手方向の寸法1〜50舊、好ましくは5〜45ルで比表
面積1.0m’/g以上、好ましくは1.5rrf/g
以上のリーフィング型又はノンリーフィング型のリン片
状の外形をした粉末である。該リン片状アルミニウム粉
末の長手方向の寸法が1μより小さい場合には高温時の
膜安定性等に劣り1反対に50戸より大きい場合には造
膜性等に劣る。また、リン片状アルミニウム粉末の比表
面積が1.0m’/gより小さい場合には造膜性に劣る
。The flaky aluminum powder used in the present invention has a longitudinal dimension of 1 to 50 mm, preferably 5 to 45 mm, and a specific surface area of 1.0 m'/g or more, preferably 1.5 rrf/g.
The powder has the above leafing type or non-leafing type scale-like external shape. If the dimension in the longitudinal direction of the scale-like aluminum powder is smaller than 1 μm, the film stability at high temperatures is poor, and on the other hand, if it is larger than 50, the film forming property is poor. Further, when the specific surface area of the flaky aluminum powder is smaller than 1.0 m'/g, the film forming property is poor.
また、リン片状アルミニウム粉末は、その表面が平滑で
ある粉末を用いることは平滑で密度の高い融合層を形成
することから有利であるゆ上記した、平滑なリン片状ア
ルミニウム粉末としては、例えば、アルミペースト52
−568(東洋アルミニウム@)、アルミペースト52
−402(東洋アルミニウムv4)、アルミペースト5
2−566 (東洋アルミニウム■)等が挙げられる。Furthermore, it is advantageous to use powder with a smooth surface because it forms a smooth and dense fusion layer. , aluminum paste 52
-568 (Toyo Aluminum @), aluminum paste 52
-402 (Toyo Aluminum v4), aluminum paste 5
2-566 (Toyo Aluminum ■) and the like.
リン片状アルミニウム粉末の配合量は、変性ポリシロキ
サン固形分100@i部に対し30〜70重量部、好ま
しくは40〜60重量部の範囲内である。該リン片状ア
ルミニウム粉末の配合量が30より少ない場合には高温
時の膜安定性等に劣り、反対に70より多い場合には、
高温時の造膜性等に劣る。The amount of flaky aluminum powder to be blended is within the range of 30 to 70 parts by weight, preferably 40 to 60 parts by weight, based on 100@i parts of the modified polysiloxane solid content. If the blending amount of the flaky aluminum powder is less than 30, the film stability at high temperatures will be poor, and on the other hand, if it is more than 70,
Poor film-forming properties at high temperatures.
本発明の耐熱性塗料組成物を調製する方法は、それ自体
既知の塗料調製方法に準じて行うことができ1例えば、
上記した変性ポリシロキサンを適出な溶剤で溶解又は分
散した後リン片状マイカ粉末及びリン片状アルミニウム
粉末を添加し高速攪拌機等の分散機で分散させることに
より耐熱性塗料組成物を得ることができる。使用しうる
溶剤としては、該変性ポリシロキサンを溶解又は分散さ
せることができるものであれば特に制限はなく、例えば
、アルコール系溶剤、ケトン系溶剤、エステル系溶剤、
芳香族系炭化水素系溶剤等が挙げられる。The method for preparing the heat-resistant coating composition of the present invention can be carried out according to a known coating preparation method.
A heat-resistant coating composition can be obtained by dissolving or dispersing the above-described modified polysiloxane in an appropriate solvent, adding scale-like mica powder and scale-like aluminum powder, and dispersing with a disperser such as a high-speed stirrer. can. The solvent that can be used is not particularly limited as long as it can dissolve or disperse the modified polysiloxane, and examples include alcohol solvents, ketone solvents, ester solvents,
Examples include aromatic hydrocarbon solvents.
さらに本発明の耐熱性塗料組成物に必要に応じて配合し
うるその他の成分として、顔料分散剤、塗面3I整剤1
着色顔料等が挙げられる。Further, as other components that can be blended as necessary in the heat-resistant coating composition of the present invention, pigment dispersants, coating surface conditioner 1
Examples include colored pigments.
本発明の耐熱性塗料組成物は、例えば、刷毛塗装、吹付
は塗装、ローラ塗装、カーテンフロー塗装、浸漬塗装等
の塗装方法で鉄素地の表面に塗布することができる。塗
1fi:は特に制限はないが、一般には乾燥膜厚20〜
50牌の範囲で充分と思われる。塗膜の乾燥は常温又は
加熱(約100〜250℃−約10〜°60分)によっ
て乾燥を行なうことができる。The heat-resistant coating composition of the present invention can be applied to the surface of an iron base by a coating method such as brush coating, spray coating, roller coating, curtain flow coating, or dip coating. Coating 1fi: There is no particular limit, but generally the dry film thickness is 20~
I think a range of 50 tiles is sufficient. The coating film can be dried at room temperature or by heating (approximately 100 to 250°C - approximately 10 to 60 minutes).
本発明の耐熱性塗料組成物は、未処理の鉄素地及びリン
酸亜鉛、リン酸鉄、クロム酸等の表面処理をほどこした
鉄素地に対して充分な高温雰囲気下での防錆性を発揮す
るが特に未処理の鉄素地に対して塗布することが経済的
にも有利である。The heat-resistant paint composition of the present invention exhibits sufficient rust prevention properties in high-temperature atmospheres on untreated iron substrates and iron substrates that have been surface-treated with zinc phosphate, iron phosphate, chromic acid, etc. However, it is economically advantageous to apply it to untreated iron substrates.
[作用]
本発明の#熱性塗料組成物より形成された塗膜が耐熱性
、防錆性にすぐれた性質を示す理由は。[Function] The reason why the coating film formed from the #thermal coating composition of the present invention exhibits excellent heat resistance and rust prevention properties is as follows.
次の様に考えられる。即ち、該塗膜が高温雰囲気(35
0°C以上)にさらされた場合に、有機質成分である変
性樹脂が無機成分を多く含むポリシロキサンよりも熱分
解温度が低いため容易に分解揮発し高濃度のアルミニウ
ム粉末及びマイカ粉末を含むものとなる。続いてポリシ
ロキサンの分解が起こり5i02の生成が始まるにつれ
て、塗膜中のアルミニウム及びマイカが素地の鉄と融合
して該素地の表面に1〜5漆(塗布膜厚20〜50延)
の鉄、アルミニウム及び珪素の防錆性を有する融合層を
形成する。また1本発明では特定のアルミニウム粉末及
びマイカ粉末を用いることにより上記の融合層が容易に
形成されるものである。It can be considered as follows. That is, the coating film is exposed to a high temperature atmosphere (35
0°C or higher), the modified resin, which is an organic component, has a lower thermal decomposition temperature than polysiloxane, which contains a large amount of inorganic components, so it easily decomposes and volatilizes, and contains high concentrations of aluminum powder and mica powder. becomes. Subsequently, as the polysiloxane decomposes and the formation of 5i02 begins, the aluminum and mica in the coating fuse with the iron of the substrate, forming a coating of lacquer 1 to 5 on the surface of the substrate (coating film thickness 20 to 50 mm).
Forms a fused layer of iron, aluminum and silicon with anti-rust properties. Further, in the present invention, the above-mentioned fused layer can be easily formed by using specific aluminum powder and mica powder.
[実施例]
次に実施例及び比較例について詳細に説明する。なお以
下実施例においての部は重量部を示す。[Example] Next, Examples and Comparative Examples will be described in detail. In addition, parts in the following examples indicate parts by weight.
実施例1〜4及び比較例1〜4
変性ポリシロキサン溶液に溶剤を添加して希釈した後、
該溶液を撹拌しながらリン片状マイカ粉末及びリン片状
アルミニウム粉末を徐々に添加し分散を行った。得られ
た分散液にディスパロン6900−20X(商品名、楠
木化成■、無機系増粘剤)を添加して粘度調整を行ない
実施例及び比較例の塗料組成物を得た。配合に用いた原
料材料及び配合割合を表−1に示す。Examples 1 to 4 and Comparative Examples 1 to 4 After adding a solvent to the modified polysiloxane solution and diluting it,
While stirring the solution, flaky mica powder and flaky aluminum powder were gradually added and dispersed. Disparon 6900-20X (trade name, Kusunoki Kasei ■, inorganic thickener) was added to the resulting dispersion to adjust the viscosity, and coating compositions of Examples and Comparative Examples were obtained. Table 1 shows the raw materials and blending ratios used for blending.
次に上記の塗料組成物を無処理のミガキ冷延鋼板にスプ
レー塗装した後、通風乾燥機中で200℃−60分間焼
付を行なって約30Pの塗装鋼板を得た。該塗装鋼板の
試験結果を表−2に示す。Next, the above coating composition was spray-painted on an untreated polished cold-rolled steel plate, and then baked in a ventilation dryer at 200°C for 60 minutes to obtain a coated steel plate of about 30P. The test results of the painted steel plate are shown in Table-2.
(月)変性ポリシロキサン
ポリエステル変性ポリシロキサン:
UD−460(60%)
バイエル合成シリコ−7株
アルキッド変性ポリシロキサン:
TSR−184(50%)
東芝シリコーン株
アクリル変性ポリシロキサン:
TSR−171(50%)
東芝シリコーン株
エポキシ変性ポリシロキサン:
TSR−194(50%)
東芝シリコーン■
(寡2)リン片状マイカ粉末
マイカS−100
[山口雲母工業所■“商品名”]
(0,1〜3終)
(家3)リン片状アルミニウム粉末
アルミペースト52−568
東洋アルミニウム株
フルイ残分(44座)1.00
%以下
試験方法
耐熱性ニブライト板に塗装した試験板を250゜350
.450.550℃で各20
時間連続加熱し、試験板を炉から取
り出した直後に注水冷却する。(Mon) Modified polysiloxane Polyester modified polysiloxane: UD-460 (60%) Bayer Synthetic Silico-7 stock alkyd modified polysiloxane: TSR-184 (50%) Toshiba Silicone Ltd. Acrylic modified polysiloxane: TSR-171 (50%) ) Toshiba Silicone Co., Ltd. Epoxy-modified polysiloxane: TSR-194 (50%) Toshiba Silicone ■ (Small 2) Scale-like mica powder Mica S-100 [Yamaguchi Mica Industries ■ "Product name"] (0,1-3 end ) (House 3) Scale-shaped aluminum powder aluminum paste 52-568 Toyo Aluminum Co., Ltd. sieve residue (44 seats) 1.00% or less Test method A test plate coated on a heat-resistant Nibrite plate was heated at 250°350°.
.. Heating was continued at 450.550°C for 20 hours each, and immediately after the test plate was taken out of the furnace, it was cooled by pouring water.
この結果塗面状態の良好な試験板 について、更にセロテープによる付 着試験を行なう。As a result, the test plate had a good coating surface condition. Furthermore, it is attached with cellophane tape. Conduct a fitting test.
[本発明の効果]
以上説明したように、本発明の耐熱性塗料組成物より得
られる塗膜は、従来の塗膜が防錆性、耐熱性を満足させ
ることができなかった問題点を改良したものでありその
効果は著しいものである。[Effects of the present invention] As explained above, the coating film obtained from the heat-resistant coating composition of the present invention has improved the problems that conventional coating films were unable to satisfy in terms of rust prevention and heat resistance. The effect is remarkable.
Claims (1)
0.01〜5μ、厚さ3000Å以下のリン片状マイカ
粉末120〜180重量部及び長手方向の寸法1〜50
μ、比表面積1.0m^2/g以上のリン片状アルミニ
ウム粉末30〜70重量部の割合で配合してなる耐熱性
塗料組成物。100 parts by weight of a modified polysiloxane component, 120 to 180 parts by weight of scale-like mica powder with a longitudinal dimension of 0.01 to 5 μ and a thickness of 3000 Å or less, and a longitudinal dimension of 1 to 50
A heat-resistant coating composition containing 30 to 70 parts by weight of scale-like aluminum powder having a specific surface area of 1.0 m^2/g or more.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16745186A JPH0822996B2 (en) | 1986-07-16 | 1986-07-16 | Heat resistant coating composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16745186A JPH0822996B2 (en) | 1986-07-16 | 1986-07-16 | Heat resistant coating composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6323975A true JPS6323975A (en) | 1988-02-01 |
JPH0822996B2 JPH0822996B2 (en) | 1996-03-06 |
Family
ID=15849937
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16745186A Expired - Lifetime JPH0822996B2 (en) | 1986-07-16 | 1986-07-16 | Heat resistant coating composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0822996B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002213705A (en) * | 2001-01-19 | 2002-07-31 | Shikoku Electric Power Co Inc | Steel product for boiler non-flame exposure part |
JP2003021370A (en) * | 2001-07-05 | 2003-01-24 | Matsushita Seiko Co Ltd | Air cleaner for smoking |
JP2009522388A (en) * | 2006-01-02 | 2009-06-11 | アクゾ ノーベル コーティングス インターナショナル ビー ヴィ | Heat resistant coating |
JP2013245414A (en) * | 2012-05-25 | 2013-12-09 | Asahi Kasei Construction Materials Co Ltd | Incombustible coating liquid, incombustible material and incombustible heat insulation panel |
JP2014122734A (en) * | 2012-12-20 | 2014-07-03 | Mitsubishi Electric Corp | Heat exchanger and heat exchanger manufacturing method |
JP2020001961A (en) * | 2018-06-28 | 2020-01-09 | 住友金属鉱山株式会社 | Heater for hydrogen sulfide reactor and manufacturing method therefor |
WO2022045045A1 (en) * | 2020-08-28 | 2022-03-03 | 中国塗料株式会社 | Paint composition, coating film, base material with coating film, and method for manufacturing same |
-
1986
- 1986-07-16 JP JP16745186A patent/JPH0822996B2/en not_active Expired - Lifetime
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002213705A (en) * | 2001-01-19 | 2002-07-31 | Shikoku Electric Power Co Inc | Steel product for boiler non-flame exposure part |
JP2003021370A (en) * | 2001-07-05 | 2003-01-24 | Matsushita Seiko Co Ltd | Air cleaner for smoking |
JP2009522388A (en) * | 2006-01-02 | 2009-06-11 | アクゾ ノーベル コーティングス インターナショナル ビー ヴィ | Heat resistant coating |
JP2013245414A (en) * | 2012-05-25 | 2013-12-09 | Asahi Kasei Construction Materials Co Ltd | Incombustible coating liquid, incombustible material and incombustible heat insulation panel |
JP2014122734A (en) * | 2012-12-20 | 2014-07-03 | Mitsubishi Electric Corp | Heat exchanger and heat exchanger manufacturing method |
JP2020001961A (en) * | 2018-06-28 | 2020-01-09 | 住友金属鉱山株式会社 | Heater for hydrogen sulfide reactor and manufacturing method therefor |
WO2022045045A1 (en) * | 2020-08-28 | 2022-03-03 | 中国塗料株式会社 | Paint composition, coating film, base material with coating film, and method for manufacturing same |
CN115989091A (en) * | 2020-08-28 | 2023-04-18 | 中国涂料株式会社 | Coating composition, coating film, substrate having coating film, and method for producing same |
Also Published As
Publication number | Publication date |
---|---|
JPH0822996B2 (en) | 1996-03-06 |
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