JPS6060165A - paint composition - Google Patents
paint compositionInfo
- Publication number
- JPS6060165A JPS6060165A JP17038983A JP17038983A JPS6060165A JP S6060165 A JPS6060165 A JP S6060165A JP 17038983 A JP17038983 A JP 17038983A JP 17038983 A JP17038983 A JP 17038983A JP S6060165 A JPS6060165 A JP S6060165A
- Authority
- JP
- Japan
- Prior art keywords
- paint
- resin
- aluminum
- parts
- manufactured
- 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
- 239000003973 paint Substances 0.000 title claims description 31
- 239000000203 mixture Substances 0.000 title claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 25
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 23
- 239000000049 pigment Substances 0.000 claims description 23
- -1 phosphorous acid trithioalcohol compound Chemical class 0.000 claims description 10
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 7
- 239000008199 coating composition Substances 0.000 claims description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- 229920005989 resin Polymers 0.000 description 20
- 239000011347 resin Substances 0.000 description 20
- 239000003795 chemical substances by application Substances 0.000 description 17
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 11
- 238000000576 coating method Methods 0.000 description 10
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 9
- 229920005862 polyol Polymers 0.000 description 9
- 150000003077 polyols Chemical class 0.000 description 9
- 239000008096 xylene Substances 0.000 description 9
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 230000002265 prevention Effects 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004606 Fillers/Extenders Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical group SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000007665 sagging Methods 0.000 description 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
- 241001061264 Astragalus Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 108091028072 EteRNA Proteins 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000006533 astragalus Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 150000002148 esters Chemical class 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
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical class O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 230000003382 ingestive effect Effects 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 210000004233 talus Anatomy 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 125000005628 tolylene group Chemical group 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明はアルミニウム顔料のリーフィング性を改良し、
かつ′F塗り、上塗りk’rtに必要とせず、−回の塗
装で仕上げることの出来るウレタン樹脂塗料組成物に関
するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention improves the leafing properties of aluminum pigments,
The present invention also relates to a urethane resin coating composition that does not require F coating or topcoat K'RT and can be finished with -2 coatings.
ところで、リーフィングタイプのアルミニウム顔料含有
エポキシ11γ1脂系塗料は鉄塔、橋梁、タンク、車両
等の塗装の如く多方面にわたり使用されているが、一方
リーフィングタイプのアルミニウム顔料含有ウレタン樹
脂塗料は、必ずしも満足のいくリーフィング性の良好な
塗膜が得られず、従ってアルミ感のある塗膜がしばしば
得られず、またエポキシ樹脂系塗料に比較し、耐水性、
耐湿性等を含めた防錆力が劣るため、未だ広く適用され
るに到ってない。Incidentally, leafing-type aluminum pigment-containing epoxy 11γ1-based paints are used in a wide variety of applications, such as painting steel towers, bridges, tanks, vehicles, etc. However, leafing-type aluminum pigment-containing urethane resin paints are not always satisfactory. It is difficult to obtain a paint film with good leafing properties, so a paint film with an aluminum feel is often not obtained, and compared to epoxy resin paints, it has poor water resistance and
It has not yet been widely applied due to its poor anti-rust properties including moisture resistance.
本発明は上記の如き現状に鑑み、アルミニウム顔料のり
一フイング性及び防錆性を改良し、広範な金属下地処理
度の被塗物に塗装出来、さらに下塗塗料と上塗塗料金兼
ね備えたリーフィングタイプのアルミニウム顔料含有ウ
レタン佃脂塗料組成物を提供することを目的とするもの
である。In view of the above-mentioned current situation, the present invention has been developed to improve the adhesion and rust prevention properties of aluminum pigments, and to develop a leafing type paint that can be coated on a wide range of metal substrates and has both an undercoat and a topcoat. The object of the present invention is to provide an aluminum pigment-containing urethane tsukuda paint composition.
このような目的はり一フイングタイプのアルシミニウム
順料金有ウつタン樹脂塗料組成物において、一般式
%式%)
)
(イ(]しnはg−λ乙の整羨文)
で示される亜リン酸トリチオアルコール化合物あるいは
その誘導体を含有することを特徴とする塗料組成物によ
って達成される。For such a purpose, in the aluminum resin coating composition of the aluminum type, the general formula %) This is achieved by a coating composition characterized by containing a trithioalcohol phosphate compound or a derivative thereof.
従来、アルミニウム顔料含有ウレタン樹脂塗料はポリオ
ール樹脂の主剤成分、号?リイノシアネートの硬化剤成
分、アルミニウムペースト成分の3液型塗料の形態で使
用されていたが、本発明の塗料組成物により亜リン酸ト
リチオアルコール化合物あるいはその誘導体全配合した
主剤成分にあらかじめアルミニウムペースト成分を混合
して保存することが出来、二液型塗料の形態も可能とな
るため曵装作業性が良好となる。またf?+られる塗膜
はリーフィング性が良く、塗j漠表面にアルミニウムフ
レークの重なった層が形成され、そのため塗膜外観がよ
く、シかも耐候性、防錆性の優れた塗膜が得られる。Conventionally, urethane resin paints containing aluminum pigments were made using polyol resin as the main component. Previously, it was used in the form of a three-component paint consisting of a curing agent component of linocyanate and an aluminum paste component, but with the paint composition of the present invention, aluminum Paste components can be mixed and stored, and a two-component paint form is also possible, which improves the workability of pouring. F again? The applied coating film has good leafing properties, and a layer of aluminum flakes is formed on the surface of the coating, resulting in a coating film with a good appearance and excellent weather resistance and rust prevention properties.
また前述の如く、本発明による塗料は下塗塗料と上塗塗
料金兼ねた機能含有するため一回の塗装で下塗り、上塗
シを兼用することが出来、塗装工程の短縮も可能となる
。Furthermore, as described above, since the paint according to the present invention has the function of serving as both an undercoat and a topcoat, it can be used as both an undercoat and a topcoat in one application, and the painting process can be shortened.
本発明のリーフィングタイプのアルミニウム顔料含有ウ
レタン樹脂塗料組成物は、主成分としてポリオール樹脂
、目?リインシアネート硬化剤、リーフィングタイツの
アルミニウム顔料および亜リン酸トリチオアルコール化
合物あるいはその誘導体からなシ、更に必要罠応じて溶
剤、防錆顔料、体質顔料、各種添加剤を配合したもので
ろる。The leafing type aluminum pigment-containing urethane resin coating composition of the present invention contains a polyol resin as a main component, and a polyol resin as a main component. It is composed of a reinocyanate curing agent, the aluminum pigment of leafing tights, and a phosphite trithioalcohol compound or its derivatives, and further contains a solvent, a rust-preventing pigment, an extender pigment, and various additives as required.
前記ポリオール樹脂としては、通常の二液型ウレタン樹
脂塗料に使用されているポリオール樹脂であればいずれ
も使用出来るが、特に防錆性を要求される個所に適用す
る場合は、エポキシ樹脂、プリエステル樹脂が好適であ
る。As the polyol resin, any polyol resin used in normal two-component urethane resin paints can be used, but when applied to areas where rust prevention is particularly required, epoxy resins and preester resins can be used. Resins are preferred.
具体的には、エポキシ樹脂としては市販のエピコート+
1009、予/θθり、イh/θθ/(以上油化シエル
エ号?キシ社製)、EPX−乙07S(地毛化工業社製
)等またポリエステル樹脂としては市販のDesmop
henRD−1g、乙θ0、Kθθ、//り0、/、2
0θ、/7θθ(以上バイエル社力叫)、パーノックD
−10(大日本インキ化学工恭社製)等が夫々代表的な
ものとして挙げられる。また、これらの工月?キシ樹脂
中の工d?キシ基の一部を、分子中に少なくとも一つの
P−OH基を有する、リン酸等の如きリンのr・/2素
1俊、そのエステルもしくはその塩と反応させた変性工
月?ギシII)を脂はそのギンート反応仕により防錆性
を一層向上せしめるので、かかる変1/l:、 、x
、1?キン樹脂を使用することが好ましい。Specifically, the commercially available epoxy resin is Epicoat +
1009, Yo/θθri, Ih/θθ/ (Yuka Cielue? Manufactured by Kishi Co., Ltd.), EPX-Otsu 07S (manufactured by Jige Ka Kogyo Co., Ltd.), etc. Also, as polyester resins, commercially available Desmop
henRD-1g, Otsu θ0, Kθθ, //ri0, /, 2
0θ, /7θθ (the above is a shoutout from Bayer), Parnock D
-10 (manufactured by Dainippon Ink Chemical Industry Co., Ltd.) are representative examples. Also, these labor months? d in resin? A modified engineering product in which a part of the xyl group is reacted with a phosphorus r./2 element such as phosphoric acid, an ester thereof, or a salt thereof, which has at least one P-OH group in the molecule. Since the oil further improves the rust prevention property due to its Ginto reaction, such change 1/l:, , x
, 1? Preferably, Kin resin is used.
尚、ポリオール4VJ脂の水酸基価けにθ〜/lりθ、
特に好ましくは10θ〜グθθが適当である。水酸基価
が前記範囲より少ないと架橋密度が低くなり防錆性肴の
塗膜性能が低下し、逆に前記範囲より大きいと架橋密度
が高く乃:りすき゛、その結果内部応力が高くなり密着
性が低下する傾向にあるのでいずれも好ましくない。In addition, for the hydroxyl value of polyol 4VJ resin, θ~/l θ,
Particularly preferably, the range is 10θ to 10θ. If the hydroxyl value is less than the above range, the crosslinking density will be low and the coating performance of the rust-preventing coating will be reduced.On the other hand, if it is larger than the above range, the crosslinking density will be high, resulting in high internal stress and poor adhesion. Both are unfavorable since they tend to decrease.
前記ポリイソシアネート硬化剤としては、トリレンジイ
ソシアネート、ノフェニルメタンソイソシア不一ト、テ
トラメチレンジイソシアネート、ヘキザメテノンジ・イ
ソシアネート、キシリレンジイソシアネート、・j?リ
メナレンポリフェニルイソシアネートあるいitこれら
インシアネートの多量体、これらイソシアネートと低分
子量の多動活性水素化合物との反工6生成物等が挙げら
れる。Examples of the polyisocyanate curing agent include tolylene diisocyanate, nophenylmethane isocyanate, tetramethylene diisocyanate, hexamethenone diisocyanate, xylylene diisocyanate, and j? Examples include rimenalene polyphenylisocyanate, polymers of these incyanates, reaction products of these isocyanates and low molecular weight hyperactive hydrogen compounds, and the like.
具体曲番では、市販されているものとして[hsmod
−ur LX[kqsmoclur N (以上バイエ
ル社)、コロネートL1コロネートHL (以上日本)
j?リウレタンエ業社が′りタケ、t、−トD 10ユ
(武田薬品工業社製入LDI−#7θ(ViJa醗酵工
業社製)等が代表的なものとして挙げられる。For specific song numbers, select commercially available [hsmod
-ur LX [kqsmoclur N (Bayer), Coronate L1 Coronate HL (Japan)
j? Typical examples include LDI-#7θ (manufactured by ViJa Hakko Kogyo Co., Ltd.) manufactured by Takeda Pharmaceutical Co., Ltd. and the like.
ポリイソシアネートの使用量は、プリオール樹脂の水酸
基/当量に対し、イソシアネート基がO0j〜d当I6
、好ましくはほぼ/当量となるような壮が適当である。The amount of polyisocyanate used is such that the isocyanate group is O0j to d per equivalent I6 based on the hydroxyl group/equivalent of the preol resin.
, preferably approximately/equivalent.
リーンインゲタイブのアルミニウム顔料としては、この
種の塗料に通常使用さ2’Lるものであればいずれも使
用できるが、特にステアリン酸等により表面処理された
ペースト状のものがよい。例えばアルドノ7″(東海金
属社製)、アルミペースト3ap (昭和アルミパウダ
ー社製)、アルペースト(東洋アルミニウム社製)、エ
ターナプライト(シルバーライン社製) 、5tapa
(旭化成工業社製)等の市販品が使用し得る。As the lean ingestive aluminum pigment, any 2'L pigment that is commonly used in this type of paint can be used, but paste-like pigments that have been surface-treated with stearic acid or the like are particularly preferred. For example, Aldono 7'' (manufactured by Tokai Kinzoku Co., Ltd.), Aluminum Paste 3ap (manufactured by Showa Aluminum Powder Co., Ltd.), Alpaste (manufactured by Toyo Aluminum Co., Ltd.), Eterna Prite (manufactured by Silver Line Co., Ltd.), 5tapa
(manufactured by Asahi Kasei Kogyo Co., Ltd.) and other commercially available products can be used.
リーフィングタイツのアルミニウム顔料の使用量は通常
ポリオール樹脂700重量部に対し5〜700M量部が
適当でるる。The amount of aluminum pigment used in leafing tights is usually 5 to 700 M parts per 700 parts by weight of the polyol resin.
本発明において、亜リン酸トリチオアルコール化合物と
しては、
一般式
%式%)
化合物あるいはこれらの混合物が使用出来る。In the present invention, as the phosphite trithioalcohol compound, a compound having the general formula % or a mixture thereof can be used.
なお、前記一般式においてn値?′ig−λ乙の整数で
ある。n値がg未満の化合物は不安定で分解し易く、逆
にn値が26を越えた化合物は、他の成分との相溶性が
悪く、いずれも好ましくない。In addition, in the above general formula, the n value? 'ig-λ is an integer. Compounds with an n value of less than g are unstable and easily decomposed, and conversely, compounds with an n value of more than 26 have poor compatibility with other components, and both are unfavorable.
また匪すンσ2トリチオアルコール化合物の誘導体とし
て、前記一般式中の直鎖状飽和チオアルコールあるいは
モノ、ジまたはトリ不飽オロデオアルコール基の7つを
、フェノール、チオフェノールあるいはその誘導イ4、
例えばアルキルフェノールもしくはアルキルチオフェノ
ール等で置換したものが使用出来る。これらの亜リン酸
トリチオアルコール化合物およびその誘導体は、そ扛自
体公知の化合物であシ、容易に入手し得る。In addition, as a derivative of the Inosun σ2 trithioalcohol compound, seven of the linear saturated thioalcohols or mono-, di- or tri-unsaturated orodeoalcohol groups in the above general formula can be substituted with phenol, thiophenol or its derivatives. ,
For example, those substituted with alkylphenol or alkylthiophenol can be used. These phosphite trithioalcohol compounds and their derivatives are known compounds per se and can be easily obtained.
前記匪リン酸トリチオアルコール化合物あるいはその誘
導体の使用量はポリオール樹脂/θoH滑部に対し3〜
100重量部、特に好ましくは3〜,2I、を滑部が適
当である。亜リン酸トリチオアルコール化合物あるいは
その誘導体の使用量が前記範囲よシ少ないと前述の如き
諸効果が期待出来ず、逆に多過き゛ると塗膜の耐水性が
極端に悪くなるためいずれも好ましくない。The amount of the trithioalcohol phosphoric acid compound or its derivative used is 3 to 3 to 100% for the polyol resin/θoH sliding part.
100 parts by weight, particularly preferably 3-2I, is suitable. If the amount of the phosphite trithioalcohol compound or its derivative used is less than the above range, the above-mentioned effects cannot be expected, and on the other hand, if it is too much, the water resistance of the coating film will be extremely poor, which is not preferable. .
本発明において、上記の亜リン酸トリチオアルコール化
合物あるいはその誘導体を配合することにより、アルミ
ニウム顔料は塗料化され長期保存した後でもリーフィン
グ性を失うことはなく、また従来のウレタン樹脂塗料に
要求されたような厳しい下地処理も不必要となシ密着性
、耐政変性等の優れた塗膜が得られる。In the present invention, by blending the above-mentioned phosphorous acid trithioalcohol compound or its derivative, the aluminum pigment is made into a paint and does not lose its leafing properties even after long-term storage, which is required for conventional urethane resin paints. A coating film with excellent adhesion and resistance to political deterioration can be obtained without the need for such severe surface treatment.
本発明において適宜使用される溶剤としてはトルエン、
キシレン、ベンゼン、ナフサ等の非極性溶剤である炭化
水素系溶剤あるいは酢酸エチル等のエステル系溶剤が適
当である。Solvents that can be used appropriately in the present invention include toluene,
Hydrocarbon solvents such as nonpolar solvents such as xylene, benzene, and naphtha, or ester solvents such as ethyl acetate are suitable.
溶剤の使用量は、ポリオール樹脂/θOM滑部に対し、
/θ〜70重景部が適当である。な分、亜リン酸トリチ
オアルコール化合物あるいはその誘導体を前記範囲内に
おいて多Kiに使用する場合には溶剤は必ずしも添加す
る必要はない。The amount of solvent used is based on the polyol resin/θOM sliding part.
/θ~70 heavy-ground area is appropriate. However, when using a phosphorous acid trithioalcohol compound or its derivative at a high Ki within the above range, it is not necessarily necessary to add a solvent.
また、本発明においては、前述のとおシ必要に応じて防
錆顔料および体質顔料を使用出来る。これらの防錆顔料
および体質顔料の使用1吋は、j?l)オール樹脂70
0重量部に対し200重量部以下が適当である。Further, in the present invention, as described above, anti-rust pigments and extender pigments can be used as necessary. 1 inch of use of these anti-rust pigments and extender pigments is j? l) All resin 70
A suitable amount is 200 parts by weight or less compared to 0 parts by weight.
以下本発明を実施例によシ詳則に説明する。なお、実施
例中「部」、「%」は重量基準で示す。The present invention will be explained in detail below using examples. In the examples, "parts" and "%" are expressed on a weight basis.
実施例/
リーフィックタイシアルミニウムR−スト顔料(アルミ
ペースト!3−//9)C東洋アルミニウム社製〕)λ
左部、亜すン酸トリチオトリラウリル/θ部およびキシ
レン3部をディスパーにて、あらかじめ練合した後ポリ
エステル樹脂[: Desmophengoo(バイエ
ル社製);水酸基価290]り0部、酢酸エチルS部お
よびダレ止め剤3部全混合し、アイス・ぐ−にて練合し
、主剤成分とした。Example / Leafic Taishi aluminum R-st pigment (aluminum paste! 3-//9) C manufactured by Toyo Aluminum Co., Ltd.]) λ
Left part, after pre-kneading trithiotrilauryl asulfite/θ parts and 3 parts of xylene in a disper, polyester resin [: Desmophengoo (manufactured by Bayer AG); hydroxyl value 290], 0 parts of ethyl acetate, S part of ethyl acetate and three parts of the anti-sagging agent were mixed together and kneaded with ice cream to form the main ingredient.
別途、トリレンジイン7アネート誘導体[Desmo−
(lurLバイエル社製)]gθ部と酢酸エチルλθ部
を混合し、硬化剤成分とした。Separately, tolylene diine 7 anate derivative [Desmo-
(manufactured by lurL Bayer AG)] gθ part and ethyl acetate λθ part were mixed to form a curing agent component.
主剤成分と硬化剤成分’k(/:/)の割合で混合し、
塗料をrarv製した。Mix the main component and curing agent component in the ratio of 'k (/:/),
The paint was made by RARV.
実施例コ
亜リン酸トリチオトリラウリルの代りに亜リン酸トリチ
オトリステアリルを使用する以外は実施例/と同様にし
て塗料を潤製した。Example A paint was prepared in the same manner as in Example except that trithiotristearyl phosphite was used instead of trithiotrilauryl phosphite.
実施例3
リーフィングタイプアルミニウムペースト顔料20部、
亜すン酸トリチオトリラウリル/θ部およびキジレンゲ
部をディスパーにてあらかじめ練合した後1.j?リエ
ステル樹脂[Desmophen /、200 (バイ
エル社製);水酸基価/7−〕660部キシレン3部2
よびダレ止め剤3部を混合し、ディスパーにで練合し主
剤成分とした。Example 3 20 parts of leafing type aluminum paste pigment,
After pre-kneading the trithiotrilauryl subsulfite/θ part and the Astragalus part in a disper, 1. j? Lyester resin [Desmophen /, 200 (manufactured by Bayer AG); hydroxyl value / 7-] 660 parts xylene 3 parts 2
and 3 parts of anti-sagging agent were mixed and kneaded in a disper to form a main ingredient.
別途、ヘキサメチレンジイソシアネート誘導体〔諏遅山
rN(バイエル社製)〕グS部と酢酸エチルS部を混合
し、硬化剤成分とした。Separately, part S of hexamethylene diisocyanate derivative [Suzayayama rN (manufactured by Bayer AG)] and part S of ethyl acetate were mixed to form a curing agent component.
主剤成分と硬化剤成分’ft−(2:/)の割合で混合
し、塗料を調製した。A paint was prepared by mixing the main component and the curing agent component at a ratio of 'ft-(2:/).
実施例り
亜リン酸トリチオトリラウリルの代りに亜リン酸トリチ
オトリカプリルを使用する以外は実施例/と同様にして
塗料(11−調製した。Example A paint (11-) was prepared in the same manner as in Example except that trithiotricapryl phosphite was used instead of trithiotrilauryl phosphite.
実施同左
リーフィングタイプアルミニウムペースト顔料20部、
亜すン酸トリチオトリオレイル/θ部およびキシレン3
部をディスパーにてめらかじめ練合した後、エポキシ樹
脂〔エピコートΦ10θ/(油化シエルエポキシ社製ン
、水酸基価37θ)1部、キシレン左t115全混合し
、ディスパーにて練合し主剤成分としたう
別途、トリレンジーfソシアネート誘導体〔コロネート
L(日本刀?リウレタンエ簗社製))11.を部と酢酸
エチルS都を混合し、硬化剤成分とした。20 parts of the same leafing type aluminum paste pigment as on the left;
Trithiotrioleyl subsulfite/θ part and xylene 3
1 part of epoxy resin [Epicoat Φ10θ/(manufactured by Yuka Ciel Epoxy Co., Ltd., hydroxyl value 37θ), 1 part of xylene left T115 were mixed together in a disper, and kneaded with a disper to obtain the main agent. Separately, as a component, trilenezi f-socyanate derivative [Coronate L (Japanese sword? Manufactured by Riurethane Yan Co., Ltd.)] 11. and ethyl acetate were mixed to form a curing agent component.
主剤成分と硬化剤成分t(,2:/)の割合で混合し塗
料を調製しシフ。Prepare a paint by mixing the main component and curing agent component at a ratio of t (,2:/) and sifting.
実施例乙
亜リン酸トリチオトリオレイルの代9に亜すン酸トリチ
オトリリルニルを使用すZ以外は実施例Sと同様VCl
−で塗料を調製した。Example O: Trithiotrilylnyl sulfite is used in place 9 of trithiotrioleyl phosphite. Same as Example S except for Z. VCl
- A paint was prepared.
比較例/
実施例/で、主剤成分において溶剤として酢酸エチルの
代りにインブタノールを使用し、亜リン酸トリチオトリ
ラウリル70部の代りに石油樹脂70部2使用する以外
は実施例/と同様にして塗料を調製した。Comparative Example/Example/The same procedure as in Example/, except that in the main component, imbutanol was used instead of ethyl acetate as a solvent, and 70 parts of petroleum resin was used instead of 70 parts of trithiotrilauryl phosphite. A paint was prepared.
比較例コ
実施例3で、主剤成分として亜リン酸トリチオトリラウ
リル10ijlLs’よびキシレン7部の代シにキシレ
ンとイソブタノールの混合物77部を使用する以外は実
施例3と同様にして塗料全調製した。Comparative Example: A paint was prepared in the same manner as in Example 3, except that 10ijlLs' of trithiotrilauryl phosphite was used as the main component and 77 parts of a mixture of xylene and isobutanol was used in place of 7 parts of xylene. did.
比較例3
実施料/で、亜リン酸トリチオトリラウリルの代υに亜
すン酸トリテオトリカグロイルを使用する以外は実施例
/と同様にして塗料を414製した。Comparative Example 3 Paint 414 was produced in the same manner as in Example 1, except that tritiotricagroyl sulfite was used in place of trithiotrilauryl phosphite.
比較例り
実施例/で亜リン酸トリチオトリラウリルの代pに亜リ
ン酸トリチオトリメリシルを使用する以外は実施例/と
同様にして塗料を調製した。Comparative Example A paint was prepared in the same manner as in Example except that trithiotrimerisyl phosphite was used in place of trithiotrilauryl phosphite.
比較例左
実施例左で、主剤成分において溶剤としてキシレン70
部の代りにキシレンとインブタノールの混合物//都*
i!2用し、亜リン酸トリチオトリオレイル10部の代
シに石油樹脂/θ都を使用する以外は実施例左と同様に
して塗料′に:+rt 蜆した。Comparative Example Left Example In the left example, xylene 70 was used as the solvent in the main component.
mixture of xylene and inbutanol instead of
i! 2 was used, and 10 parts of trithiotrioleyl phosphite was replaced with petroleum resin/θ in the same manner as in Example left.
実施例/〜乙、2よび比較例/〜左で調製した主剤成分
を一定期間保存後、硬化剤成分と混合しこの塗料全刷毛
にて乾燥膜厚100μになるように)開板上に塗布し、
/週間自然乾燥させた後、リーフィング性を目視判定し
た。その結果ヶ第1表に示す。After storing the main component prepared in Example/~B, 2 and Comparative Example/~left for a certain period of time, it was mixed with a curing agent component and applied to the open plate using a full brush to a dry film thickness of 100μ. ,
After natural drying for /week, leafing property was visually judged. The results are shown in Table 1.
第7表
判定基準 (O←(つ−Δ→ ×
メタリック感良好 メタリック感殆どなしまた実施例/
〜乙および比較例7〜Sで調製し7c、a料tす717
2ラスト鉄板(S i S 、 Sa 、:2. ’/
)、)と錆鉄板(2tillり一しン)VC−刷毛にて
乾燥膜厚100μi(二なるように塗布し、/週間自然
乾燥させた後、クロスカットし、1M水噴霧試験(左0
θ時間)および屋外:1暴露試験(/年間)をし、その
結果ケ第λ表に示す。Table 7 Judgment Criteria (O←(TS-Δ→ × Good metallic feel Almost no metallic feel Also Examples/
~B and Comparative Examples 7~S 7c and a materials 717
2 last iron plate (S i S , Sa , :2.'/
), ) and a rusted iron plate (2till resin) VC-Apply with a brush in a dry film thickness of 100 μi (two coats, let dry naturally for a week, cross-cut, 1M water spray test (left 0
θ time) and outdoors: 1 exposure test (/year) was conducted and the results are shown in Table λ.
第7表および第−表よシ明らかな如く、本発明の塗料は
、長期間保存後もリーフィング性良好で、メタリック感
の良好な塗膜が得らノt1 また防錆性も浚J’してい
た。一方、木発すJで使用する煎りン戚トリチオアルコ
ール化合物を配合しない比較例/〜左の塗料Q1、長期
間保存後の塗料のr1M膜はメタリック感が劣り、また
防錆性も劣っていた。As is clear from Table 7 and Table 1, the paint of the present invention has good leafing properties even after long-term storage, and a coating film with a good metallic feel can be obtained. was. On the other hand, the paint Q1 on the left, the r1M film of the paint Q1 on the left, which does not contain the trithioalcohol compound used in Kibatsu J, had a poor metallic feel and poor rust prevention properties. .
Claims (1)
脂塗料組成物において、 一般式 %式%) ) (但し、nはg〜λ乙の整数) で示される亜リン酸トリチオアルコール化合物あるいは
その誘4体を含イ1することを特徴とする塗料料組成物
。[Claims] A leafing-type aluminum pigment-containing urethane resin coating composition comprising a phosphorous acid trithioalcohol compound represented by the general formula %) (where n is an integer from g to λ) or 1. A paint composition characterized by containing a diurethane.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17038983A JPS6060165A (en) | 1983-09-14 | 1983-09-14 | paint composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17038983A JPS6060165A (en) | 1983-09-14 | 1983-09-14 | paint composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6060165A true JPS6060165A (en) | 1985-04-06 |
| JPS6322233B2 JPS6322233B2 (en) | 1988-05-11 |
Family
ID=15904020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17038983A Granted JPS6060165A (en) | 1983-09-14 | 1983-09-14 | paint composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6060165A (en) |
-
1983
- 1983-09-14 JP JP17038983A patent/JPS6060165A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6322233B2 (en) | 1988-05-11 |
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