JP2021046523A - 水性樹脂組成物、コーティング剤、及び物品 - Google Patents
水性樹脂組成物、コーティング剤、及び物品 Download PDFInfo
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- JP2021046523A JP2021046523A JP2019171610A JP2019171610A JP2021046523A JP 2021046523 A JP2021046523 A JP 2021046523A JP 2019171610 A JP2019171610 A JP 2019171610A JP 2019171610 A JP2019171610 A JP 2019171610A JP 2021046523 A JP2021046523 A JP 2021046523A
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Abstract
Description
示される構造を有することが好ましい。下記一般式(6)で示される構造を有するア
ルキルトリアルコキシシランの縮合物に由来のポリシロキサンセグメントは、三次元網目状のポリシロキサン構造を有することから、得られる塗膜は、耐溶剤性、耐候性などに優れたものである。
攪拌機、温度計、滴下ロート、冷却管及び窒素ガス導入口を備えた反応容器に、メチルトリメトキシシラン(以下、「MTMS」と略記する。)1,421質量部を仕込んで、60℃まで昇温した。次いで、前記反応容器中にiso−プロピルアシッドホスフェート(堺化学株式会社製「A−3」、以下「触媒(1)」と略記する。)0.17質量部と脱イオン水207質量部との混合物を5分間で滴下した後、80℃の温度で4時間撹拌して加水分解縮合反応させた。
合成例1と同様の反応容器に、プロピレングリコールモノプロピルエーテル(以下、「PnP」と略記する。)36質量部、イソプロピルアルコール(以下、「IPA」と略記する。)80質量部、フェニルトリメトキシシラン(以下、「PTMS」と略記する。)32質量部及びジメチルジメトキシシラン(以下、「DMDMS」と略記する。)19質量部を仕込んで、80℃まで昇温した。次いで、同温度でメチルメタクリレート(以下、「MMA」と略記する。)99質量部、ブチルメタクリレート(以下、「BMA」と略記する。)86質量部、ブチルアクリレート(以下、「BA」と略記する。)67質量部、アクリル酸(以下、「AA」と略記する。)16質量部、3−メタクリルオキシプロピルトリメトキシシラン(以下、「MPTS」と略記する。)5質量部、PnP14質量部及びtert−ブチルパーオキシ−2−エチルヘキサノエート(以下、「TBPEH」と略記する。)14質量部を含有する混合物を、前記反応容器中へ4時間で滴下し、滴下終了後、更に同温度で2時間反応させてカルボキシル基と珪素原子に結合した加水分解性基を併有する数平均分子量が18,000の重合体(a’−1)を得た後、触媒(1)0.9質量部と脱イオン水24質量部との混合物を、5分間で滴下し、更に同温度で10時間撹拌して加水分解縮合反応を行ない、カルボキシル基と珪素原子に結合した加水分解性基を併有する重合体セグメントとPTMS及びDMDMS由来のポリシロキサンセグメントからなる複合樹脂(A’B−1)を得た。次いで、TEA18質量部を添加して複合樹脂(A’B−1)中のカルボキシル基を中和して複合樹脂(AB−1)とした後、メチルトリメトキシシランの縮合物(c−1)124質量部を添加し、更に、脱イオン水550質量部を添加して、加水分解縮合による前記複合樹脂(AB−1)とメチルトリメトキシシランの縮合物(c−1)由来のポリシロキサンセグメント(C−1)が結合した複合樹脂(ABC−1)の生成と、複合樹脂(ABC−1)の水性媒体中への分散を行ない、複合樹脂(ABC−1)の水性分散体を得た。次いで、得られた水性分散体を、40〜1.3kPaの減圧下、温度40〜60℃の条件で2時間蒸留することにより、IPA、生成したメタノール及び水を除去して、不揮発分が40.0%の複合樹脂(ABC−1)の水性分散体1,000質量部を得た。
合成例2で得られた複合樹脂(ABC−1)の水性分散体100質量部、ジプロピレングリコールモノブチルエーテル5質量部、3−メルカプトプロピルトリメトキシシラン(以下、「シランカップリング剤(D−1)」と略記する。)5質量部、及び硬化剤(日清紡ケミカル株式会社製「カルボジライト E―05」、ポリカルボジイミド樹脂;以下、「硬化剤(1)」と略記する。)10質量部を均一に混合し、水性樹脂組成物(1)を得た。
実施例1で使用したシランカップリング剤(D−1)を、トリエトキシシリルチオプロピルトリメトキシシラン(以下、「シランカップリング剤(D−2)」と略記する。)に変更した以外は、実施例1と同様にして、水性樹脂組成物(2)を得た。
実施例1で使用したシランカップリング剤(D−1)を、ビス(トリエトキシシリルプロピル)テトラスルフィド(以下、「シランカップリング剤(D−3)」と略記する。)に変更した以外は、実施例1と同様にして、水性樹脂組成物(3)を得た。
実施例1で使用したシランカップリング剤(D−1)を、3−オクタノイルチオ−1−プロピルトリエトキシシラン(以下、「シランカップリング剤(D−4)」と略記する。)に変更した以外は、実施例1と同様にして、水性樹脂組成物(4)を得た。
合成例2で得られた複合樹脂(ABC−1)の水性分散体100質量部、可塑剤(DIC株式会社製「モノサイザーW−260」)5質量部、シランカップリング剤(D−2)1質量部、及び3−グリシドキシプロピルトリメトキシシラン(以下、「硬化剤(2)」と略記する。)6質量部を均一に混合し、水性樹脂組成物(5)を得た。
実施例5で使用したシランカップリング剤(D−2)1質量部を、3質量部に変更した以外は、実施例5と同様にして、水性樹脂組成物(6)を得た。
実施例5で使用したシランカップリング剤(D−2)1質量部を、10質量部に変更した以外は、実施例5と同様にして、水性樹脂組成物(7)を得た。
実施例5で使用したシランカップリング剤(D−2)1質量部を、30質量部に変更した以外は、実施例5と同様にして、水性樹脂組成物(8)を得た。
実施例1で使用したシランカップリング剤(D−1)5質量部を、使用しなかった以外は、実施例1と同様にして、水性樹脂組成物(R1)を得た。
実施例1で使用したシランカップリング剤(D−1)5質量部を、シランカップリング剤(D−2)50質量部に変更した以外は、実施例1と同様にして、水性樹脂組成物(R2)を得た。
実施例1で使用したシランカップリング剤(D−1)を、3−イソシアネートプロピルトリメトキシシラン(以下、「シランカップリング剤(RD−1)」と略記する。)に変更した以外は、実施例1と同様にして、水性樹脂組成物(R3)を得た。
実施例1で使用したシランカップリング剤(D−1)を、3−アミノプロピルトリメトキシシラン(以下、「シランカップリング剤(RD−2)」と略記する。)に変更した以外は、実施例1と同様にして、水性樹脂組成物(R4)を得た。
株式会社エンジニアリングテストサービス製のクロメート処理されたアルミ板に各下塗り塗料を乾燥後の膜厚が20μmとなるよう塗装し、25℃の環境下で1日間乾燥させた後、上記で得た水性樹脂組成物を乾燥後の膜厚が20μmとなるように塗装し、25℃の環境下で1週間乾燥させて評価用硬化塗膜を得た。下塗り塗料A〜Dを用いて得られた評価用硬化塗膜をそれぞれ評価用硬化塗膜A〜Dとした。
下塗り塗料A:2液型アクリル系塗料(DIC株式会社製「アクリディック WDT−600」/DIC株式会社製「バーノック DN−990」=100/24(質量部)
下塗り塗料B:アクリル系塗料(DIC株式会社製「アクリディック A−1370−LS」)
下塗り塗料C:2液型フルオロオレフィン系塗料(DIC株式会社製「フルオネート K−704」/DIC株式会社製「バーノック DN−980」=100/18(質量部)
下塗り塗料D:2液型フルオロオレフィン系塗料(DIC株式会社製「フルオネート WFQ−396」/DIC株式会社製「バーノック DN−990」=100/14(質量部)
上記で得られた評価用硬化塗膜Aを目視で観察し、下記の基準で塗膜外観を評価した。
○:クラックの発生が認められない。
△:若干のクラックの発生が認められる。
×:クラックの発生が認められる。
上記で得られた評価用硬化塗膜Aについて、デューパネル光ウェザーメーター(スガ試験機株式会社製、光照射時:30W/m2、70℃;湿潤時:湿度90%以上、50℃、光照射/湿潤サイクル=8時間/4時間)で1,000時間曝露を行なった後の塗膜を目視で観察し、下記の基準で塗膜外観を評価した。
○:クラックの発生が認められない。
△:若干のクラックの発生が認められる。
×:クラックの発生が認められる。
作製直後の評価用硬化塗膜Aの鏡面反射率(光沢値)(%)と、評価用硬化塗膜Aを、デューパネル光ウェザーメーター(スガ試験機株式会社製、光照射時:30W/m2、70℃;湿潤時:湿度90%以上、50℃、光照射/湿潤サイクル=8時間/4時間)で1,000時間曝露した後の塗膜の鏡面反射率(光沢値)(%)の、曝露前の硬化塗膜の鏡面反射率(光沢値)に対する保持率(光沢保持率:%)〔(100×曝露後の塗膜の鏡面反射率)/(曝露前の硬化塗膜の鏡面反射率)〕で評価した。保持率の値が大きいほど、耐候性が良好であることを示す。鏡面反射率はBYK株式会社製のマイクロ−トリ−グロスを用いて測定した。
上記で得られた評価用硬化塗膜について、大阪府高石市のDIC株式会社堺工場内において3か月間曝露を行なった。曝露試験後の未洗浄の塗膜と、曝露試験前の塗膜との色差(ΔE)を、コニカミノルタセンシング株式会社製「CM−3500d」を用いて評価した。前記色差(ΔE)が小さいほど、耐汚染性が良好であることを示す。
上記で得られた評価用硬化塗膜A〜Dについて、JIS K−5600 碁盤目試験法に基づいて測定した。前記硬化塗膜の上にカッターで1mm幅の切込みを入れ碁盤目の数を100個とし、全ての碁盤目を覆うようにセロハンテープを貼り付け、すばやく引き剥がして付着して残っている碁盤目の数を数え、下記の基準で評価した。
○:はがれなし。
△:はがれの面積は、全碁盤目面積の1〜65%未満。
×:はがれの面積は、全碁盤目面積の65%以上。
上記で得られた評価用硬化塗膜A〜Dについて、50℃の温水に7日間浸漬した後に温水から取り出した直後の外観を目視で観察し、下記の基準で評価した。
○:白化が認められない。
△:白化が認められる。
×:基材からの剥がれが認められる。
上記で得られた評価用硬化塗膜A〜Dについて、50℃の温水に7日間浸漬した後に温水から取り出し1時間静置した。その後、塗膜の上にカッターで1mm幅の切込みを入れ碁盤目の数を100個とし、全ての碁盤目を覆うようにセロハンテープを貼り付け、すばやく引き剥がして付着して残っている碁盤目の数を数え、下記の基準で評価した。
○:はがれなし。
△:はがれの面積は、全碁盤目面積の1〜65%未満。
×:はがれの面積は、全碁盤目面積の65%以上。
Claims (5)
- 中和された酸基を有する重合体セグメント(A)及びポリシロキサンセグメント(B)が化学結合した複合樹脂(AB)のポリシロキサンセグメント(B)と、アルキル基の炭素原子数が1〜3のアルキルトリアルコキシシランの縮合物(c)由来のポリシロキサンセグメント(C)とが珪素−酸素結合を介して結合している複合樹脂(ABC)が水性媒体中に溶解又は分散し、さらに硫黄原子を有するシランカップリング剤(D)を含有している水性樹脂組成物であり、前記複合樹脂(ABC)中の前記ポリシロキサンセグメント(B)及び前記ポリシロキサンセグメント(C)の合計の含有比率が15〜85質量%の範囲であり、前記複合樹脂(ABC)100質量部に対する前記シランカップリング剤(D)の含有量が0.1〜100質量部の範囲であることを特徴とする水性樹脂組成物。
- 請求項1又は2記載の水性樹脂組成物を含有することを特徴とするコーティング剤。
- 請求項3記載のコーティング剤の硬化塗膜を有することを特徴とする複層塗膜。
- 請求項3記載のコーティング剤の硬化塗膜を有することを特徴とする物品。
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JPH0782453A (ja) * | 1993-09-10 | 1995-03-28 | Kanegafuchi Chem Ind Co Ltd | 硬化性樹脂組成物 |
JPH11181347A (ja) * | 1997-12-22 | 1999-07-06 | Kanegafuchi Chem Ind Co Ltd | 塗料用硬化性樹脂組成物 |
JP2011190308A (ja) * | 2010-03-12 | 2011-09-29 | Dic Corp | 水性硬化性樹脂組成物およびその製造方法 |
JP2012031382A (ja) * | 2010-07-08 | 2012-02-16 | Dic Corp | 水性硬化性塗料組成物、及びその製造方法 |
Cited By (1)
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WO2023135884A1 (ja) * | 2022-01-17 | 2023-07-20 | テルモ株式会社 | シリンジ用ガスケットおよびそれを備えたシリンジ |
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