JPWO2016006664A1 - 赤外反射性顔料及び赤外反射性塗料組成物 - Google Patents
赤外反射性顔料及び赤外反射性塗料組成物 Download PDFInfo
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- JPWO2016006664A1 JPWO2016006664A1 JP2016532971A JP2016532971A JPWO2016006664A1 JP WO2016006664 A1 JPWO2016006664 A1 JP WO2016006664A1 JP 2016532971 A JP2016532971 A JP 2016532971A JP 2016532971 A JP2016532971 A JP 2016532971A JP WO2016006664 A1 JPWO2016006664 A1 JP WO2016006664A1
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- Prior art keywords
- infrared reflective
- layer
- reflective pigment
- pigment
- infrared
- 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.)
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- C—CHEMISTRY; METALLURGY
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- C—CHEMISTRY; METALLURGY
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Abstract
Description
[赤外反射性顔料]
本実施形態に係る赤外反射性顔料は、高い赤外光反射性と高い可視光透過性を兼ね備えた鱗片状(扁平状)の顔料である。本実施形態に係る赤外反射性顔料は、塗膜中に配合されたときに、塗膜面に対してその扁平面が平行になるように配向することで、より高い赤外反射性と高い可視光透過性を発現する。
本実施形態に係る赤外反射性顔料は、少なくとも1層の金属薄膜層と、少なくとも2層の透明な誘電体層と、を有する積層体を備える。
なお、本実施形態に係る赤外反射性顔料1の積層体13は、図1に示す5層構造に限定されず、少なくとも1層の金属薄膜層11と、少なくとも2層の透明な誘電体層12とを有していればよく、層数は限定されないが、金属薄膜層11と誘電体層12が交互に積層されていることが好ましい。
以下、金属薄膜層11、誘電体層12、表面処理層14及び表面張力調整層15の各層の構成について、詳細に説明する。
なお、金属薄膜層11を複数層有する場合、製造上の観点からは各金属薄膜層11を同一の材料から構成することが好ましいが、各金属薄膜層11を異なる材料から構成してもよい。
なお、製造上の観点から各誘電体層12を同一の材料から構成することが好ましいが、各誘電体層12を異なる材料から構成してもよい。
ここで、可視光周辺域の波長は、可視光域である380〜780nm及びその周辺域であり、具体的には180〜980nmが該当する。屈折率nは、例えばHORIBA製やJ.A.Woolam JAPAN製のエリプソメータにより測定可能である。
具体的には、例えば図1に示す5層構造の赤外反射性顔料1では、中央に配置された誘電体層12の膜厚はλ/2n(光学膜厚はλ/2)であり、最も外側に配置された2つの誘電体層12の膜厚はλ/4n(光学膜厚はλ/4)である。
[第1製造方法]
図2は、本実施形態に係る赤外反射性顔料1の第1製造方法を示す図である。図2に示すように、赤外反射性顔料1の第1製造方法は、支持体10上に金属薄膜層11及び誘電体層12からなる積層体13を形成する工程(以下、金属薄膜層及び誘電体層形成工程という)と、当該積層体13を支持体10から剥離する工程(以下、剥離工程という)と、当該積層体13を粉砕する工程(以下、粉砕工程という)と、を有する。
支持体10としては、透明でも不透明でもよく、金属材料、高分子材料、酸化物材料、ガラス等が用いられる。
塗布方法としては、例えば、ロールコーティング法、ロッドバーコーティング法、エアナイフコーティング法、スプレーコーティング法、スライド型カーテン塗布法、スライドホッパー(スライドビード)塗布法、エクストルージョンコート法等が挙げられる。
金属薄膜溶液及び誘電体溶液の塗布量は、乾燥後の膜厚が上述の金属薄膜層11及び誘電体層12の各層の好ましい膜厚の範囲内となるように、適宜設定される。
例えば、後述するように超音波水浴中に浸漬させることにより、支持体10から積層体13を剥離することができる。上述したように、支持体10として水溶性フィルム以外の材料を用いた場合には、支持体10の表面に剥離層を設けることで、支持体10上に形成した積層体13を容易に剥離できる。また、支持体10として水溶性フィルムを用いた場合には、水中に浸漬するだけで支持体10が溶解し、容易に積層体13を剥離することができる。
粉砕方法としては、例えば、粉砕機による機械的粉砕、振動ミル、ボールミル、ジェットミル等を用いた湿式粉砕、乾式粉砕が用いられる。湿式粉砕する場合、溶媒としては、積層体13の構成成分が溶解しない溶媒であればよく、例えば、水;メタノール、エタノール、イソプロパノール、n−ブチルアルコール、t−ブチルアルコール、エチレングリコール等のアルコール類;アセトン、メチルエチルケトン等のケトン類;酢酸エチル等のエステル類;クロロホルム、塩化メチレン等のハロゲン化物;ブタン、ヘキサン等のオレフィン類;テトラヒドロフラン(THF)、ブチルエーテル、ジオキサン等のエーテル類;ベンゼン、キシレン、トルエン等の芳香族類;N,N−ジメチルホルムアミド(DMF)、ジメチルアセトアミド(DMAc)等のアミド類;及びこれらの混合溶媒であってもよい。乾式で粉砕する際には、積層体13を液体窒素等で冷却して、硬い状態としてから粉砕してもよい。
表面処理層14の形成方法としては、例えば、加熱分解法、中和加水分解法、ゾルゲル法等が挙げられる。これらの方法により、積層体13の端面部にも均一に表面処理層14が形成され、赤外反射性顔料1の表面全体を表面処理層14で被覆できる。
また、ゾルゲル法では、有機金属化合物等の溶液を加水分解・重縮合させ、ゾルを形成した後にゲル化する。その後、加熱することにより、金属酸化物からなる表面処理層14が得られる。
表面張力調整層15の形成方法としては、従来公知の浸漬法が用いられる。具体的には、例えば、ステアリン酸と石油蒸留物を含む溶液中に、表面処理層14が形成された積層体13を分散させ、超音波バス中で処理する。次いで、分散物を吸引濾過して溶媒で洗浄した後、乾燥する。これにより、積層体13の表面に形成された表面処理層14を被覆する表面張力調整層15が得られる。
図3は、本実施形態に係る赤外反射性顔料1の第2製造方法を示す図である。図3に示すように、赤外反射性顔料1の第2製造方法は、支持体10A上に、金属薄膜層及び誘電体層を形成することで積層体13を得る工程(以下、金属薄膜層及び誘電体層形成工程という)と、支持体10Aを含む積層体13を粉砕する工程(以下、粉砕工程という)と、を有する。第2製造方法は、剥離工程を設けず、支持体10Aが赤外反射性顔料1の一部を構成する点において、第1製造方法と相違する。
粉砕工程、表面処理層形成工程及び表面張力調整層形成工程は、第1製造方法と同様である。
本実施形態に係る赤外反射性塗料組成物は、上述の赤外反射性顔料1を含有する塗料組成物である。
本実施形態に係る赤外反射性塗料組成物は、上述の赤外反射性顔料1と、樹脂成分と、を主成分として含有する。塗料タイプとしては、有機溶剤型塗料、NAD系、水性塗料、エマルション塗料、コロイダル塗料、紛体塗料等が挙げられる。本実施形態に係る赤外反射性塗料組成物は、従来公知の方法により製造される。
[数1]
顔料面密度(%)=WCA(cm2/g)×PWC(%)×塗膜比重(g/cm3)×膜厚(cm)
[数2]
PWC(%)=顔料/(樹脂固形分+不揮発成分(添加剤等)+顔料)
本実施形態に係る赤外反射性塗料組成物を塗装する際、前述の通り、塗装時の塗料固形分を調整し、赤外反射性塗膜収縮により本発明の赤外反射性顔料が高配向に配列するようにすることが好ましい。
赤外反射性塗料組成物を塗装した後の乾燥工程は、本発明の赤外反射性顔料を高配向に配列する観点で、60〜200℃が好ましく、80〜160℃がより好ましい。
可視光透過率及び日射取得率の測定は、JIS−R3106:1998「板ガラス類の透過率・反射率・放射率・日射熱取得率の試験方法」に準拠した方法に従って実施することができる。
表1に示す配合に従って、実施例1〜13及び比較例1〜4の赤外反射性塗料組成物を調製した。実施例1〜3、5〜11、13及び比較例1〜4は、上述の第1製造方法により赤外反射性顔料1を調製し、実施例4、12は、上述の第2製造方法により赤外反射性顔料1Aを調製した。
先ず、支持体10として、50×50×2mmのガラス板(TP技研製)に、アクリル樹脂(アクリディック A−1371 DIC社製)を酢酸ブチルを用いて10質量%(固形分換算)となるように調製した後、スピンコーターにて乾燥膜厚が1μmとなるように塗布した。その後、80℃で15分間乾燥し、剥離層を形成した。
支持体10Aとして、50mm×50mm×0.5μmの天然マイカ板(ヤマグチマイカ社製)を用い、基材の両面に、誘電体層及び金属層を設けたこと以外は、実施例1と同様にし、赤外反射性顔料1Aを得た。
実施例1〜13及び比較例1〜4では、可視光周辺域の入射光の波長λを300nmとし、表1に示した膜厚となるように、誘電体層及び金属薄膜層を形成した。
具体的には、誘電体層に用いた二酸化チタン(ルチル型)、酸化亜鉛及びITOの光学膜厚と実際の膜厚は、以下の表2に示した通りである。他の誘電体層及び金属薄膜層の光学膜厚も、同様にλ/4を算出してλ/4の整数倍±10nmとなるようにして、実際の膜厚を設定した。
なお、膜厚制御は、水晶発振式製膜コントローラ(アルバック社製「CRTM−6000G」)にて行った。
各実施例及び比較例の赤外反射性塗膜について、可視光透過率及び日射取得率の測定を実施した。可視光透過率及び日射取得率の測定は、JIS−R3106:1998「板ガラス類の透過率・反射率・放射率・日射熱取得率の試験方法」に準拠した方法に従って実施した。測定に用いた分光光度装置は、島津製作所社製の分光光度計(型番:UV3600)であった。結果を表1に示した。
各実施例及び比較例の赤外反射性塗膜について、超促進耐候性(SUV)試験を実施した。試験後の塗膜を、目視にて劣化度合いを評価した。試験条件及び評価基準は以下の通りとした。結果を表1に示した。
(試験条件)
測定試験機:サンシャインウェザーメーター「S80−B−H」
光照射強度:850W/cm2
照射時間:600時間
(評価基準)
3:外観上、問題が無い。
2:塗膜外観が若干白ボケて半透明であり、やや劣化が見られる。
1:塗膜外観が白ボケて透明性が失われており、劣化が見られる。
10,10A…支持体
11…金属薄膜層
12…誘電体層
13…積層体
14…表面処理層
15…表面張力調整層
Claims (8)
- 鱗片状の赤外反射性顔料であって、
少なくとも1層の金属薄膜層と、少なくとも2層の透明な誘電体層と、を有する積層体を備え、
可視光周辺域の入射光の波長をλとし且つ前記誘電体層の屈折率をnとしたときに、前記誘電体層の膜厚が(λ/4nの整数倍)±10nmであることを特徴とする赤外反射性顔料。 - 前記金属薄膜層が、銀、アルミニウム、銅、金、パラジウム、亜鉛、チタン、クロム及び珪素からなる群より選択される少なくとも1種からなることを特徴とする請求項1に記載の赤外反射性顔料。
- 前記誘電体層が、二酸化チタン、酸化亜鉛、酸化アルミニウム、酸化ジルコニウム、二酸化ケイ素、酸化錫、錫添加酸化インジウム及びアンチモン添加酸化錫からなる群より選択される少なくとも1種からなることを特徴とする請求項1又は2に記載の赤外反射性顔料。
- 前記積層体の表面を被覆し且つ酸化物からなる表面処理層をさらに備えることを特徴とする請求項1から3いずれかに記載の赤外反射性顔料。
- 前記表面処理層が、酸化アルミニウム、シリカ及び酸化ジルコニウムからなる群より選択される少なくとも1種からなることを特徴とする請求項4に記載の赤外反射性顔料。
- 前記表面処理層の表面を被覆し且つ表面張力調整剤からなる表面張力調整層をさらに備えることを特徴とする請求項4又は5に記載の赤外反射性顔料。
- 前記表面張力調整層が、ステアリン酸を含む表面張力調整剤からなることを特徴とする請求項6に記載の赤外反射性顔料。
- 請求項1から7いずれかに記載の赤外反射性顔料を含有する赤外反射性塗料組成物。
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EP3168266A4 (en) | 2018-01-10 |
US10131790B2 (en) | 2018-11-20 |
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JP6162901B2 (ja) | 2017-07-12 |
CN106574129A (zh) | 2017-04-19 |
CN106574129B (zh) | 2019-03-15 |
WO2016006664A1 (ja) | 2016-01-14 |
US20170174893A1 (en) | 2017-06-22 |
EP3168266A1 (en) | 2017-05-17 |
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