JPH0228627B2 - JIDOSHA YOSHIIRINGUZAI - Google Patents
JIDOSHA YOSHIIRINGUZAIInfo
- Publication number
- JPH0228627B2 JPH0228627B2 JP5948185A JP5948185A JPH0228627B2 JP H0228627 B2 JPH0228627 B2 JP H0228627B2 JP 5948185 A JP5948185 A JP 5948185A JP 5948185 A JP5948185 A JP 5948185A JP H0228627 B2 JPH0228627 B2 JP H0228627B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- weight
- resin
- sealant
- 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.)
- Expired - Lifetime
Links
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 25
- 239000000565 sealant Substances 0.000 claims description 23
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 21
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 11
- 239000003822 epoxy resin Substances 0.000 claims description 8
- 239000004014 plasticizer Substances 0.000 claims description 8
- 229920000647 polyepoxide Polymers 0.000 claims description 8
- 239000004645 polyester resin Substances 0.000 claims description 8
- 229920001225 polyester resin Polymers 0.000 claims description 8
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 8
- 238000009835 boiling Methods 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 4
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 description 12
- 238000000576 coating method Methods 0.000 description 12
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 9
- 229910000831 Steel Inorganic materials 0.000 description 7
- 230000002265 prevention Effects 0.000 description 7
- 239000010959 steel Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 4
- 239000002518 antifoaming agent Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000035699 permeability Effects 0.000 description 4
- 229920006122 polyamide resin Polymers 0.000 description 4
- -1 P-cymentetralin Chemical compound 0.000 description 3
- 239000010428 baryte Substances 0.000 description 3
- 229910052601 baryte Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 150000001733 carboxylic acid esters Chemical class 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 239000003759 ester based solvent Substances 0.000 description 2
- 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 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000007665 sagging Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- WJECKFZULSWXPN-UHFFFAOYSA-N 1,2-didodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1CCCCCCCCCCCC WJECKFZULSWXPN-UHFFFAOYSA-N 0.000 description 1
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- LTEQMZWBSYACLV-UHFFFAOYSA-N Hexylbenzene Chemical compound CCCCCCC1=CC=CC=C1 LTEQMZWBSYACLV-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 150000002168 ethanoic acid esters Chemical class 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
Description
(産業上の利用分野)
本発明は、自動車用の鋼板合せ目に塗布し鋼板
合せ目内への水分、塩分等の侵入による錆等の発
生を防止する自動車用シーリング剤に関する。
(従来の技術)
従来、前記の自動車用シーリング剤は、塩ビ系
樹脂と可塑剤と炭酸カルシウムとを塗膜形成用主
成分とするものは公知である。
(発明が解決しようとする問題点)
前記従来のシーリング剤は炭酸カルシウムの配
合によつて厚膜化を図ると共に可塑剤の配合によ
つて粘性を得るようにしていたが、可塑剤の配合
量に限界が有り、粘度を700〜900ポイズ位にしか
調節できず、浸透性が不十分で膜厚が一定せず、
膜厚の厚い部分は外観不良をもたらし、また膜厚
の薄い部分は防錆性に欠けるという不都合を有す
る。また、かかる不都合を防止すべく、シーリン
グ剤の塗布後に筆びきを行なうようにしている
が、筆びき後に中塗り、上塗りを施しても筆跡が
表面に浮き出てくるスケ不良が発生するという不
都合を有する。
(問題点を解決するための手段)
本発明は、上記従来の欠点を解消し、シーラー
ガンによる押出し塗布又はスプレー塗布のみの1
工程塗布を可能にし、塗布作業性を改善し、防錆
性、耐久性、耐湿性等の向上したしかも塗膜の外
観が良好な自動車用シーリング剤を提供するもの
で、ウレタン樹脂、又はエポキシ樹脂、又はポリ
エステル樹脂100重量部に対して炭酸カルシウム
25〜70重量部、硫酸バリウム65〜200重量部及び
沸点が150℃以上の芳香族又は/及びエステル系
溶剤50〜150重量部を配合して成り、可塑剤を含
まないことを特徴とする。
(実施例)
次に本発明の実施例につき詳述する。
塗膜形成用主成分である樹脂としては、可塑剤
の併用を要しないウレタン樹脂、エポキシ樹脂、
ポリエステル樹脂を使用する。
これら樹脂を架橋硬化させるために硬化剤成分
として、各種変性ポリアミン、ポリアミド樹脂、
ポリオール樹脂、メラミン樹脂、ユリア樹脂等の
従来公知の硬化剤の中から適宜選択し、前記樹脂
の種類に応じて該樹脂に当量数配合してもよい。
体質顔料としては、特に、炭酸カルシウムと硫
酸バリウムとの配合を必須とし、炭酸カルシウム
は、塗塗後の塗膜の厚膜化や耐薬品性及び耐衝撃
性の向上に寄与するものであり、その配合量は、
ウレタン樹脂、又はエポキシ樹脂、又はポリエス
テル樹脂100重量部に対し25〜70重量部とする。
25重量部未満であると前記の諸効果は得られず、
70重量部を超えると塗膜が脆くなるおそれがあ
る。硫酸バリウムは、塗装後のシーリング剤の厚
膜表面を平滑化するに必要であり、その配合量
は、ウレタン樹脂、又はエポキシ樹脂、又はポリ
エステル樹脂100重量部に対し65〜200重量部とす
る。65重量部未満であると、前記の諸効果が得ら
れず、200重量部を超えると塗膜が脆くなる恐れ
がある。
尚、前記本発明自動車用シーリング剤には、着
色顔料を少量添加することが一般である。例え
ば、酸化チタン、カーボンブラツク、タルク、マ
イカ、カオリン、炭酸マグネシウム、エロジー
ル、ヒル石、グラフアイト、アルミナ、シリカ等
の粉末を適量、例えばウレタン樹脂、又はエポキ
シ樹脂、又はポリエステル樹脂100重量部に対し
4〜25重量部配合する。
溶剤は、粘度調整の目的の他、ダレ、ワキの発
生防止並に浸透性、レベリング性の向上を目的と
して、沸点が150℃以上の芳香族又は/及びエス
テル系溶剤を、ウレタン樹脂、又はエポキシ樹
脂、又はポリエステル樹脂100重量部に対し、50
〜150重量部を配合する。50重量部未満だと塗布
作業に必要な粘度に調整できないおそれがあり、
150重量部を超えると塗布作業及び防錆性能が低
下するおそれがある。そして沸点が150℃以上の
芳香族溶剤としては、ジエチルベンゼン、イソプ
ロピルベンゼン、トリアミルベンゼン、テトラア
ミルベンゼン、ジドデシルベンゼン、アミルトル
エン、P−シメンテトラリン、デカリン、ジペン
テン、P−メンタンなどで、沸点が150℃以上の
石油系溶剤を1種又は2種以上使用する。エステ
ル系溶剤としては、酢酸エステル、コハク酸エス
テル、グルタル酸エステル、アジピン酸エステ
ル、カルボン酸エステル、スルホン酸エステル、
無機酸エステル、グリセリンのエステルなどの1
種又は2種以上を使用する。
又、これらの沸点が150℃以上の芳香族溶剤及
びエステル系溶剤を混ぜて使用してもよい。
その他の添加剤類として、防錆効果を向上させ
るために、鉛粉、亜鉛化鉛、亜鉛黄、ストロンチ
ウムクロメート、鉛丹、塩基性クロム酸塩などを
適宜混入でき、又消泡剤、増粘剤、防腐剤、分散
剤、揺変剤、凍結防止剤、PH調整剤等を配合する
ことができる。
本発明の自動車用シーリング剤は、自動車ボデ
イの電着塗料焼付塗装後、例えばその鋼板の合わ
せ目に、シーラーガンにより或はエアースプレ
ー、エアレススプレーなどにより帯状に塗装する
に当り、通常、その塗膜の乗りやスプレー性等か
ら通常20〜500ポイズ(20℃)の範囲内に調整す
ることが好ましい。その塗装時点は、電着塗料焼
付後、上塗塗装前であれば任意の段階で行なつて
よく、従来の可塑剤を含むシーリング剤のよう
に、前記焼付後、中塗塗装工程前までに限定され
ることなく自由に選定可能である。塗装部位も、
特に限定されることはないが、主に、自動車ボデ
イ鋼板の合わせ目間隔が2m/m以下のドアー下
回り、エンジンルーム部合わせ目、テールゲイト
付近に使用される。又鋼板合わせ目間隔によりシ
ーリング剤の粘度を適宜調整することが好まし
い。
次に更に具体的な実施例を従来例と共に詳述す
る。
実施例 1
ウレタン樹脂(商品名タケネートB−830、武
田薬品工業株式会社製)100重量部にポリアミド
樹脂(商品名エポキユア3080、油化シエルエポキ
シ株式会社製)20重量部を配合した樹脂材100重
量部に対し、炭酸カルシウム(商品名カルシーズ
PL、神鳥化学工業株式会社製)33重量部、硫酸
バリウム(商品名バライトBC、堺化学工業株式
会社)100重量部、溶剤として酢酸エステル100重
量部、消泡剤(商品名BYK−0、ビツクマリン
クロツト社製)8重量部、分散剤(商品名デイス
パロン#1250、楠本化成株式会社製)8重量部を
配合し均一に混練して本発明の自動車用シーリン
グ剤を得た。
実施例 2
エポキシ樹脂(商品名エピコート828、油化シ
エルエポキシ株式会社製)100重量部にポリアミ
ド樹脂(商品名エポキユア3080、油化シエルエポ
キシ株式会社製)42重量部を配合した樹脂材100
重量部に対し、炭酸カルシウム(商品名カルシー
ズPL、神島化学工業株式会社製)33重量部、硫
酸バリウム(商品名バライトBC、堺化学工業株
式会社)100重量部、溶剤としてエチルベンゼン
とカルボン酸エステルの混合溶剤100重量部、消
泡剤(商品名BYK−0、ビツクマリンクロツト
社製)7重量部、分散剤(商品名デイスパロン
#1250、楠本化成株式会社製)7重量部を配合し
均一に混練して本発明の自動車用シーリング剤を
得た。
実施例 3
ポリエステル樹脂(商品名ベツコライトM−
6402−50、大日本インキ化学工業株式会社製)
100重量部にメラミン樹脂(商品名スーパーベツ
カミンL−109−65、大日本インキ化学工業株式
会社製)42重量部を配合した樹脂材100重量部に
対し、炭酸カルシウム(商品名カルシーズPL、
神島化学工業株式会社製)33重量部、硫酸バリウ
ム(商品名バライトBC、堺化学工業株式会社)
100重量部、溶剤としてエチルベンゼンとカルボ
ン酸エステルの混合溶剤100重量部、消泡剤(商
品名BYK−0、ビツクマリンクロツト社製)7
重量部、分散剤(商品名デイスパロン#1250、楠
本化成株式会社製)7重量部を配合し均一に混練
して本発明の自動車用シーリング剤を得た。
従来例
ポリ塩化ビニール樹脂(商品名ゼオン400×
110A、日本ゼオン株式会社製)100重量部に対
し、炭酸カルシウム(商品名カルシーズPL、神
島化学工業株式会社製)400重量部、可塑剤とし
てフタル酸エステル200重量部、酸化チタン(商
品名タイペークR−820、石原産業株式会社製)
14重量部、ポリアミド樹脂(商品名エポキユア
3080、油化シエルエポキシ株式会社製)18重量部
を配合し均一に混練して従来の自動車用シーリン
グ剤を得た。
これらのシーリング剤につき、下記の7項目に
つき、試験し、下記表1に示す試験結果を得た。
(Field of Industrial Application) The present invention relates to a sealant for automobiles that is applied to the joints of steel plates for use in automobiles to prevent the occurrence of rust due to the intrusion of moisture, salt, etc. into the joints of steel plates. (Prior Art) Conventionally, the above-mentioned sealing agent for automobiles is known which contains a vinyl chloride resin, a plasticizer, and calcium carbonate as main components for forming a coating film. (Problems to be Solved by the Invention) The conventional sealants mentioned above have been made to thicken the film by adding calcium carbonate and to obtain viscosity by adding a plasticizer. The viscosity can only be adjusted to between 700 and 900 poise, and the film thickness is not constant due to insufficient permeability.
The thicker portions give rise to poor appearance, while the thinner portions lack rust prevention. In addition, in order to prevent such inconveniences, brush strokes are performed after applying the sealant, but even if an intermediate coat or top coat is applied after brush strokes, the inconvenience that the handwriting will stand out on the surface and cause sagging defects will occur. have (Means for Solving the Problems) The present invention solves the above-mentioned conventional drawbacks, and solves the above-mentioned conventional problems by applying only extrusion coating using a sealer gun or spray coating.
We provide an automotive sealant that enables process coating, improves coating workability, has improved rust prevention, durability, moisture resistance, etc., and has a good appearance of the paint film, and is made of urethane resin or epoxy resin. , or calcium carbonate per 100 parts by weight of polyester resin
25 to 70 parts by weight, 65 to 200 parts by weight of barium sulfate, and 50 to 150 parts by weight of an aromatic or/and ester solvent having a boiling point of 150°C or higher, and is characterized by not containing a plasticizer. (Example) Next, an example of the present invention will be described in detail. The resins that are the main components for coating film formation include urethane resins, epoxy resins, and epoxy resins that do not require the use of plasticizers.
Use polyester resin. In order to crosslink and cure these resins, various modified polyamines, polyamide resins,
The curing agent may be appropriately selected from conventionally known curing agents such as polyol resins, melamine resins, and urea resins, and may be blended in equivalent amounts with the resin depending on the type of the resin. As an extender pigment, it is especially essential to combine calcium carbonate and barium sulfate. Calcium carbonate contributes to thickening the coating film and improving chemical resistance and impact resistance after application. Its blending amount is
The amount is 25 to 70 parts by weight per 100 parts by weight of urethane resin, epoxy resin, or polyester resin.
If it is less than 25 parts by weight, the above effects cannot be obtained,
If it exceeds 70 parts by weight, the coating film may become brittle. Barium sulfate is necessary to smooth the surface of the thick film of the sealant after painting, and its amount is 65 to 200 parts by weight per 100 parts by weight of urethane resin, epoxy resin, or polyester resin. If it is less than 65 parts by weight, the above-mentioned effects cannot be obtained, and if it exceeds 200 parts by weight, the coating film may become brittle. Incidentally, a small amount of coloring pigment is generally added to the above-mentioned sealant for automobiles of the present invention. For example, an appropriate amount of powder of titanium oxide, carbon black, talc, mica, kaolin, magnesium carbonate, erosil, vermiculite, graphite, alumina, silica, etc., per 100 parts by weight of urethane resin, epoxy resin, or polyester resin. Add 4 to 25 parts by weight. The solvent is an aromatic or/and ester solvent with a boiling point of 150°C or higher, urethane resin, or epoxy, for the purpose of adjusting viscosity, preventing sagging and wrinkles, and improving permeability and leveling. 50 parts per 100 parts by weight of resin or polyester resin
~150 parts by weight is blended. If it is less than 50 parts by weight, it may not be possible to adjust the viscosity to the level required for coating work.
If it exceeds 150 parts by weight, the coating work and rust prevention performance may deteriorate. Examples of aromatic solvents with a boiling point of 150°C or higher include diethylbenzene, isopropylbenzene, triamylbenzene, tetraamylbenzene, didodecylbenzene, amyltoluene, P-cymentetralin, decalin, dipentene, and P-menthane. Use one or more petroleum solvents with a temperature of 150℃ or higher. Ester solvents include acetate, succinate, glutarate, adipate, carboxylate, sulfonate,
Inorganic acid esters, glycerin esters, etc.
Use one species or two or more species. Further, aromatic solvents and ester solvents having a boiling point of 150° C. or higher may be used in combination. As other additives, lead powder, zincated lead, zinc yellow, strontium chromate, red lead, basic chromate, etc. can be mixed as appropriate in order to improve the rust prevention effect, and antifoaming agents and thickeners can be added. Agents, preservatives, dispersants, thixotropic agents, antifreeze agents, PH adjusters, etc. can be added. The automotive sealant of the present invention is usually applied to the joints of steel plates after baking the electrocoated paint on the car body, for example, when it is applied in a band shape using a sealer gun, air spray, airless spray, etc. It is usually preferable to adjust the temperature within the range of 20 to 500 poise (20°C) from the viewpoint of film rideability, sprayability, etc. The application can be carried out at any stage after the baking of the electrodeposition paint and before the top coat is applied; unlike conventional sealants containing plasticizers, it is limited to after the baking and before the intermediate coat. It is possible to freely select the The painted parts are also
Although not particularly limited, it is mainly used under doors, engine room joints, and near tailgates where the seam spacing of automobile body steel plates is 2 m/m or less. Further, it is preferable to adjust the viscosity of the sealant as appropriate depending on the spacing between the steel plates. Next, a more specific embodiment will be described in detail together with a conventional example. Example 1 100 parts by weight of a resin material prepared by blending 100 parts by weight of a urethane resin (trade name Takenate B-830, manufactured by Takeda Pharmaceutical Co., Ltd.) with 20 parts by weight of a polyamide resin (trade name Epoqueure 3080, manufactured by Yuka Ciel Epoxy Co., Ltd.) Calcium carbonate (trade name: Calseeds)
33 parts by weight of barium sulfate (product name: Barite BC, manufactured by Sakai Chemical Industry Co., Ltd.), 100 parts by weight of acetic acid ester as a solvent, antifoaming agent (product name: BYK-0, BITSU) 8 parts by weight of a dispersant (trade name: Disparon #1250, manufactured by Kusumoto Kasei Co., Ltd.) were blended and uniformly kneaded to obtain a sealant for automobiles of the present invention. Example 2 Resin material 100 was prepared by blending 100 parts by weight of an epoxy resin (trade name Epicote 828, manufactured by Yuka Ciel Epoxy Co., Ltd.) with 42 parts by weight of a polyamide resin (trade name Epoqueure 3080, manufactured by Yuka Ciel Epoxy Co., Ltd.).
Based on the weight part, 33 parts by weight of calcium carbonate (trade name: Calseeds PL, manufactured by Kamishima Chemical Industry Co., Ltd.), 100 parts by weight of barium sulfate (trade name: Barite BC, manufactured by Sakai Chemical Industry Co., Ltd.), ethylbenzene and carboxylic acid ester as a solvent. 100 parts by weight of a mixed solvent, 7 parts by weight of an antifoaming agent (product name: BYK-0, manufactured by Bitzkumarinkrodt Co., Ltd.), and 7 parts by weight of a dispersant (product name: Disparon #1250, manufactured by Kusumoto Kasei Co., Ltd.) were mixed uniformly. The mixture was kneaded to obtain an automotive sealant of the present invention. Example 3 Polyester resin (trade name Betsukolite M-
6402-50, manufactured by Dainippon Ink & Chemicals Co., Ltd.)
Calcium carbonate (product name: Calcease PL,
33 parts by weight (manufactured by Kamishima Chemical Industry Co., Ltd.), barium sulfate (trade name Barite BC, Sakai Chemical Industry Co., Ltd.)
100 parts by weight, 100 parts by weight of a mixed solvent of ethylbenzene and carboxylic acid ester as a solvent, antifoaming agent (trade name: BYK-0, manufactured by Bitzkumarinkrodt) 7
and 7 parts by weight of a dispersant (trade name Disparon #1250, manufactured by Kusumoto Kasei Co., Ltd.) were blended and uniformly kneaded to obtain an automotive sealant of the present invention. Conventional example: Polyvinyl chloride resin (product name: Zeon 400×
110A, manufactured by Nippon Zeon Co., Ltd.), 400 parts by weight of calcium carbonate (product name: Calseeds PL, manufactured by Kamishima Chemical Industry Co., Ltd.), 200 parts by weight of phthalate ester as a plasticizer, titanium oxide (product name: Taipeke R) −820, manufactured by Ishihara Sangyo Co., Ltd.)
14 parts by weight, polyamide resin (trade name: Epoqueure)
3080 (manufactured by Yuka Ciel Epoxy Co., Ltd.) was blended with 18 parts by weight and kneaded uniformly to obtain a conventional sealant for automobiles. These sealants were tested for the following seven items, and the test results shown in Table 1 below were obtained.
【表】
下記項目の試験方法は次のように行なつた。
1 浸透性試験
間隔を100μとした鋼板合わせ目に、シーリン
グ剤20mlを塗布した後、垂直に立てゝ140℃で焼
付けた。このときシーリング剤が浸透した距離が
20m/m以上であつたものを良好とし〇で表示し
た。
2 外観試験
電着塗料焼付後の各試験板に、実施例1,2,
3の各シーリング剤については夫々その200μを
シーラーガンにより塗布したのみで筆びきは行な
わず、一方従来例のシーリング剤の方はその
1000μをシーラーガンにより塗布後、筆びきし、
その後これら各試験板に更に中塗20μ、上塗り
40μを塗装してから外観上の塗面の凹凸及びスケ
を調べた。外観上の塗面の凹凸及びスケのないも
のを〇で表示した。
3 防錆力試験
2項と同様に上塗塗装までした各塗装試験板に
中央の金属板に達するまでナイフカツトを入れ、
JIS−K−5400に規定された塩水噴霧試験機に240
時間入れ、カツト部よりの錆巾を測定した。
4 耐久性試験
2項と同様に作成した各塗装試験板を、サン
シヤインウエザーメーター600時間、次で、50
℃、98%湿潤試験機72時間を6サイクル経過後、
0.2m/m角テープ剥離を調べた。
剥離しなかつたものを〇で表示した。
5 耐湿性試験
2項と同様に作成した各塗装試験板を50℃、98
%湿潤試験機240時間経過後、0.2m/m角テープ
剥離及び表面のふくれを調べた。剥離なく且つふ
くれのないものを〇で表示した。
6 引張強度試験
鋼板に形成したシーリング剤の単独塗膜をJIS
−K−6300に準じダンベル2号で50m/m分で引
張つた。
7 剪断接着試験
6項で同様の単独塗膜をJIS−K−6300に準じ
スペーサ3m/mで50m/m分で引張つた。前記の
表1から明らかなように、実施例1,2,3の自
動車用シーリング剤は従来例の自動車用シーリン
グ剤と比較して、浸透性、外観、防錆力、耐久
性、耐湿性、引張強度、剪断接着強度の全ての点
において優れていた。
(発明の効果)
このように、本発明の自動車用シーリング剤に
よるときは、樹脂成分100重量部に対して炭酸カ
ルシウム25〜70重量部、硫酸バリウム65〜200重
量部及び沸点が150℃以上の芳香族又は/及びエ
ステル系溶剤50〜150重量部を配合して可塑剤を
含まないようにしたために、作業性をはじめ、防
錆性、耐久性、耐湿性等に優れると共に塗膜の外
観も良好であるという効果を有する。[Table] The test methods for the following items were performed as follows. 1. Permeability test After applying 20ml of sealant to the joints of the steel plates with a spacing of 100μ, the sheets were stood vertically and baked at 140°C. At this time, the distance that the sealant penetrated was
Those with a velocity of 20 m/m or more are considered to be good and marked with a circle. 2 Appearance test Examples 1, 2,
For each sealant in No. 3, 200μ of each was applied with a sealer gun without brushing, while the conventional sealant
After applying 1000μ with a sealer gun, brush
After that, each of these test boards was further coated with 20μ intermediate coat and top coat.
After painting 40μ, the appearance of the painted surface was examined for unevenness and scratches. Items with no unevenness or scratches on the painted surface were marked with a circle. 3 Rust prevention power test Insert a knife cut into each coated test plate that has been coated with top coat in the same way as in Section 2 until it reaches the metal plate in the center.
240 to the salt spray tester specified in JIS-K-5400
After some time, the rust depth from the cut portion was measured. 4 Durability test Each coated test board prepared in the same manner as in Section 2 was tested on a sunshine weather meter for 600 hours and then for 50 hours.
℃, after 6 cycles of 72 hours in a 98% humidity tester,
Peeling of a 0.2m/m square tape was investigated. Those that did not peel off were marked with a circle. 5 Moisture resistance test Each coated test plate prepared in the same manner as in Section 2 was heated at 50°C and 98°C.
% humidity tester After 240 hours, peeling of the 0.2 m/m square tape and surface blistering were examined. Those with no peeling and no blistering were marked with a circle. 6 Tensile strength test A single coating film of sealant formed on a steel plate was tested according to JIS
- Pulled at 50m/m with dumbbell No. 2 according to K-6300. 7. Shear adhesion test A single coating film similar to that described in Section 6 was stretched at 50 m/m with a spacer of 3 m/m according to JIS-K-6300. As is clear from Table 1 above, the automotive sealants of Examples 1, 2, and 3 have better permeability, appearance, rust prevention, durability, moisture resistance, and better performance than the conventional automotive sealants. It was excellent in both tensile strength and shear adhesive strength. (Effects of the Invention) As described above, when using the automotive sealant of the present invention, 25 to 70 parts by weight of calcium carbonate, 65 to 200 parts by weight of barium sulfate, and a material having a boiling point of 150°C or higher are added to 100 parts by weight of the resin component. By blending 50 to 150 parts by weight of an aromatic or/and ester solvent to avoid plasticizers, it has excellent workability, rust prevention, durability, moisture resistance, etc., and the appearance of the coating film. It has the effect of being good.
Claims (1)
エステル樹脂100重量部に対して炭酸カルシウム
25〜70重量部、硫酸バリウム65〜200重量部及び
沸点が150℃以上の芳香族又は/及びエステル系
溶剤50〜150重量部を配合して成り、可塑剤を含
まないことを特徴とする自動車用シーリング剤。1 Calcium carbonate per 100 parts by weight of urethane resin, epoxy resin, or polyester resin
25 to 70 parts by weight of barium sulfate, 65 to 200 parts by weight of barium sulfate, and 50 to 150 parts by weight of an aromatic or/and ester solvent with a boiling point of 150°C or higher, and does not contain a plasticizer. Sealant for use.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5948185A JPH0228627B2 (en) | 1985-03-26 | 1985-03-26 | JIDOSHA YOSHIIRINGUZAI |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5948185A JPH0228627B2 (en) | 1985-03-26 | 1985-03-26 | JIDOSHA YOSHIIRINGUZAI |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61218679A JPS61218679A (en) | 1986-09-29 |
| JPH0228627B2 true JPH0228627B2 (en) | 1990-06-25 |
Family
ID=13114540
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5948185A Expired - Lifetime JPH0228627B2 (en) | 1985-03-26 | 1985-03-26 | JIDOSHA YOSHIIRINGUZAI |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0228627B2 (en) |
-
1985
- 1985-03-26 JP JP5948185A patent/JPH0228627B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61218679A (en) | 1986-09-29 |
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