JPS6338069B2 - - Google Patents

Info

Publication number
JPS6338069B2
JPS6338069B2 JP57132155A JP13215582A JPS6338069B2 JP S6338069 B2 JPS6338069 B2 JP S6338069B2 JP 57132155 A JP57132155 A JP 57132155A JP 13215582 A JP13215582 A JP 13215582A JP S6338069 B2 JPS6338069 B2 JP S6338069B2
Authority
JP
Japan
Prior art keywords
parts
resin
unsaturated
glitter
plastic film
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
Application number
JP57132155A
Other languages
Japanese (ja)
Other versions
JPS5922746A (en
Inventor
Seiichi Takano
Katsuhisa Morita
Eiichiro Takyama
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Resonac Holdings Corp
Original Assignee
Showa Highpolymer Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Showa Highpolymer Co Ltd filed Critical Showa Highpolymer Co Ltd
Priority to JP57132155A priority Critical patent/JPS5922746A/en
Publication of JPS5922746A publication Critical patent/JPS5922746A/en
Publication of JPS6338069B2 publication Critical patent/JPS6338069B2/ja
Granted legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Laminated Bodies (AREA)

Description

【発明の詳现な説明】[Detailed description of the invention]

本発明は、塗料、印刷むンキ、泚型および繊維
匷化プラスチツクなどの甚途に䟛され、補品にき
らめきのある頗る矎麗な倖芳を䞎える暹脂組成物
に関する。 埓来、材料の劂䜕を問わず、䟋えば挆塗りにお
ける螺田、或いは宝石のオパヌルにみられるきら
めきのある倖芳を有する人工の成圢品は、それが
無機系のものであるにせよ、有機系のものである
にせよ、実際問題ずしお造られおはいない。 アルミニりムパりダヌのように鱗片状の着色剀
を塗料に入れお、補品にわづかにきらめきのある
感芚を持たせようずする詊みはなされおいる。 しかし、これずおも本栌的なきらめきのある虹
色を補品に䞎えるずい぀た点では満足すべきもの
ではなく、むしろた぀たく異質の倖芳を補品に䞎
えるずい぀た方が圓぀おいよう。 近幎、矎的芁求の高たりに䌎぀お、補品に単な
る色付けを斜しただけでは需芁の高床化に远埓す
るこずは困難ずなり、より優れた感芚を備えた補
品を求める動きは著しい。 䟋えば、前述した螺田を䟋にずるず、呚知のよ
うに螺田は、黒挆地に所望の暡様に仕䞊げた真珠
光沢を有する貝殻を接着したものであるが、その
高雅な倖芳は高玚品ずしお定評があり、このよう
な補品は他にみるこずができない。 本発明者らは、虹色のきらめきのある矎麗な倖
芳を有する成圢品を埗るために皮々怜蚎した結
果、特定の倚局プラスチツクフむルム现片ず、特
定の液状暹脂からなる暹脂組成を塗料、印刷むン
キ、泚型および繊維匷化プラスチツクなどの甚途
に䟛した堎合、補品に虹色のきらめきのある矎麗
な倖芳を䞎えるこずを芋出し、本発明を完成する
に至぀た。 即ち、本発明は、屈折率の異なる少なくずも
皮の透明なプラスチツクフむルムが亀互に10局以
䞊積局された倚局プラスチツクフむルム现片ず、
該倚局プラスチツクフむルム现片を膚最ないし溶
解しない液状暹脂からなる暹脂組成物に関する。 本発明においお䜿甚される倚局プラスチツクフ
むルム现片は、プラスチツクフむルムの䞀局の厚
みがミクロン単䜍たたはそれ以䞋で、しかも屈折
率の異なる少なくずも皮のプラスチツクフむル
ムが亀互に10局以䞊、奜たしくは50局以䞊積局さ
れ、そしお所望の倧きさに切断されたものであ぀
お、光の干枉䜜甚によ぀お頗る矎麗な虹色のきら
めきを呈するものである。同䞀屈折率のプラスチ
ツクフむルムからなる倚局プラスチツク现片を甚
いた堎合は、本発明の効果が埗られない。 切断する倧きさは、目的に応じお遞定される。
䟋えば、建材のように倧型の補品を補造する堎合
には、倚局プラスチツクフむルム现片が䜙り小さ
くおは芋栄えがせず、通垞は0.3〜mm䜍に切断
されたものが奜たしい。たた、むンテリア郚品、
装食品などの補造に䜿甚する堎合には、倚局プラ
スチツクフむルム现片の倧きさは0.1〜0.5mm皋床
が適しおいる。 倚局プラスチツクフむルム现片以䞋、きらめ
き付䞎剀ずいうを構成する透明なプラスチツク
フむルムの皮類は特に制限はされないが、䞀般に
はポリ塩化ビニル屈折率1.52〜1.53、ポリス
チレン屈折率1.59〜1.60、ポリプロピレン
屈折率1.49、ポリメチルメタクリレヌト屈折
率1.48〜1.50、メチルメタクリレヌト―スチレ
ン共重合䜓屈折率1.56〜1.57、ポリカヌボネ
ヌト1.58〜1.59およびポリ゚ステル1.65
等の熱可塑性暹脂からなるフむルムが甚いられ
る。 きらめき付䞎剀は、屈折率の異なる少なくずも
皮のプラスチツクフむルムが亀互に10局以䞊、
奜たしくは50局以䞊積局されおおれば、その積局
順序は特に制限されない。ここでいう亀互ずは、
䟋えば屈折率ず屈折率の皮のプラスチツク
フむルムからなるきらめき付䞎剀の積局順序は、
ABABAB

ABの順序に積局されおいるこず
を意味する。たた、屈折率、屈折率および屈
折率の皮のプラスチツクフむルムからなるき
らめき付䞎剀の積局順序は、ABCABC

ABC
の順序に積局されおいおもよいし、たた
ABCBCACAB

CBA等の順序に積局されお
いおもよいこずを意味する。即ち、屈折率の異な
るプラスチツクフむルムを皮以䞊䜿甚する堎合
は、同䞀屈折率のプラスチツクフむルムが連続し
お局以䞊積局されないこずを意味する。 屈折率の異なる少なくずも皮のプラスチツク
フむルムの積局数が10局未満では、補品にきらめ
きのある倖芳を䞎えるこずは困難である。 本発明においお、きらめき付䞎剀ず䜵甚しお䜿
甚される液状暹脂ずしおは、次蚘のものがあげら
れる。 (ã‚€) モノマヌ類の䜵甚なしに硬化する、アクリロ
むル基CH2CH―CO―、たたはメタクリロむ
ル基
The present invention relates to a resin composition that is used in paints, printing inks, casting molds, fiber-reinforced plastics, and the like, and gives products a shimmering and strikingly beautiful appearance. Conventionally, regardless of the material, for example, artificial molded products that have a shimmering appearance such as lacquered lacquer or opal jewelry are made of organic or inorganic materials. However, it has not been created as a practical matter. Attempts have been made to incorporate scaly colorants, such as aluminum powder, into paints to give the product a slightly shimmering feel. However, it is not satisfactory to say that it imparts a very authentic shimmering iridescent color to the product; rather, it would be more accurate to say that it imparts a dazzling and foreign appearance to the product. In recent years, as aesthetic requirements have increased, it has become difficult to keep up with the increasing sophistication of demand by simply adding color to products, and there has been a significant movement toward products with a superior tactility. For example, taking the above-mentioned raita as an example, as is well known, raita is made by gluing pearlescent shells finished in a desired pattern onto a black lacquer base, but its elegant appearance makes it a luxury item. It has a reputation as such, and you won't find a product like this anywhere else. As a result of various studies in order to obtain a molded product with a beautiful appearance with rainbow-colored sparkles, the present inventors discovered that a resin composition consisting of specific multilayer plastic film strips and a specific liquid resin could be used in paints and printing inks. The present inventors have discovered that when used in applications such as casting and fiber-reinforced plastics, they can give products a beautiful appearance with iridescent sparkles, leading to the completion of the present invention. That is, the present invention provides at least two different refractive indexes.
A multilayer plastic film strip in which 10 or more layers of transparent plastic film are alternately laminated;
The present invention relates to a resin composition comprising a liquid resin that does not swell or dissolve the multilayer plastic film strips. The multilayer plastic film strip used in the present invention has a thickness of each layer of plastic film in microns or less, and has at least 10 layers, preferably 50 layers or more, of at least two types of plastic films having different refractive indexes alternately. It is laminated and cut into desired sizes, and exhibits a beautiful iridescent sparkle caused by the interference of light. If a multilayer plastic strip made of plastic films with the same refractive index is used, the effects of the present invention cannot be obtained. The size to be cut is selected depending on the purpose.
For example, when manufacturing large-sized products such as building materials, if the multilayer plastic film strips are too small, it will not look good, so it is usually preferable to cut the multilayer plastic film into pieces of about 0.3 to 1 mm. In addition, interior parts,
When used for manufacturing decorative items, etc., the suitable size of the multilayer plastic film strips is about 0.1 to 0.5 mm. The type of transparent plastic film constituting the multilayer plastic film strip (hereinafter referred to as the glitter imparting agent) is not particularly limited, but generally polyvinyl chloride (refractive index 1.52 to 1.53) or polystyrene (refractive index 1.59 to 1.60) is used. , polypropylene (refractive index 1.49), polymethyl methacrylate (refractive index 1.48-1.50), methyl methacrylate-styrene copolymer (refractive index 1.56-1.57), polycarbonate (1.58-1.59) and polyester (1.65)
Films made of thermoplastic resins such as The glitter-imparting agent consists of 10 or more alternate layers of at least two types of plastic films with different refractive indexes,
Preferably, as long as 50 or more layers are laminated, the lamination order is not particularly limited. What is meant by alternation here?
For example, the lamination order of the glitter-imparting agent consisting of two types of plastic films with refractive index A and refractive index B is as follows:
ABABAB means that they are stacked in the order of AB. Furthermore, the lamination order of the glitter imparting agent consisting of three types of plastic films with refractive index A, refractive index B, and refractive index C is ABCABC...ABC
may be stacked in the order of
ABCBCACAB...means that they may be stacked in the order of CBA, etc. That is, when three or more types of plastic films having different refractive indexes are used, it means that two or more layers of plastic films having the same refractive index are not successively laminated. If the number of laminated layers of at least two types of plastic films with different refractive indexes is less than 10, it is difficult to give the product a shimmering appearance. In the present invention, examples of the liquid resin used in combination with the glitter-imparting agent include the following. (a) Acryloyl group CH 2 =CH-CO- or methacryloyl group that cures without the use of monomers

【匏】 を分子䞭に個以䞊有する䞍飜和メタア
クリレヌト系オリゎマヌ。 䟋えば、ポリ゚ステル〜メタアクリレヌ
ト類、ビニル゚ステル暹脂、スピロアセタヌル
〜メタアクリレヌト類、りレタン〜メ
タアクリレヌト類、分子量200以䞊の倚䟡ア
ルコヌルのポリメタアクリレヌト類、トリ
スヒドロキシアルキルむ゜シアヌレヌトのメ
タアクリレヌト、ポリ゚ヌテル〜メタア
クリレヌト類、メチロヌルメラミンの䞍飜和ア
ルコヌルの゚ヌテル。 ビニル゚ステル暹脂ずしおは、゚ポキシ〜
メタアクリレヌトず、倚䟡プノヌルたた
はノボラツクのアルキレンオキシド付加物のポ
リメタアクリレヌトずが含たれる。以䞊の
オリゎマヌの䜵甚は自由である。たた、これら
のオリゎマヌは、倚局プラスチツクフむルム现
片を溶解しない溶剀たたはモノマヌず䜵甚する
こずは差支えない。 (ロ) 䞍飜和スピロアセタヌル、或いはアリル゚ヌ
テル型䞍飜和結合を分子䞭に個以䞊含む䞍
飜和シクロアセタヌルずポリチオヌル化合物ず
の混合䜿甚系。 䟋えば、ゞアリリデンペンタ゚リスリツトず
ペンタ゚リスリツトのテトラチオグリコレヌト
ずの反応暹脂。 (ハ) アミン類、アミン付加物たたは液状ポリアミ
ドを硬化剀ずする゚ポキシ暹脂。 酞無氎物を甚いる高枩硬化も利甚可胜である
が、特に利点が認められない䞊、高枩で長時間
の加熱はきらめきを損う傟向がある。 本発明は、きらめき付䞎剀ず、このきらめき付
䞎剀を膚最ないし溶解しない液状暹脂ず䜵甚する
こずよりなり、これを泚型、加熱成圢、塗装、印
刷、或いは撒垃等の方法により、暹脂自䜓、たた
は察象ずなる玠材たたは成圢品に虹色を呈するき
らめきを付䞎するこずにある。 きらめき付䞎剀を構成するプラスチツクフむル
ムを溶解する溶剀乃至液状暹脂をビヒクルに甚い
るず、このきらめきある虹色は完党に消倱し、ご
みの混入したようなた぀たく芋栄えのしない倖芳
しか埗られない。 このために、芳銙族炭化氎玠類、゚ステル類、
ケトン類、ハロゲン化炭化氎玠類、ニトロパラフ
むン類のごずき、通垞ビヒクルずしお甚いられる
溶剀乃至スチレン、メタクリル酞゚ステル類、ア
クリル酞゚ステル類、酢酞ビニル等のごずきモノ
マヌは、フむルムを構成するプラスチツクの皮類
にもよるが、䞀般にビヒクルずしおは甚いられな
い。 埓぀お、これら溶剀或いはモノマヌを成分ず
する暹脂、塗料、むンキ等もきらめき付䞎剀ずの
䜵甚は、プラスチツクフむルムを構成するポリマ
ヌがこれら溶剀或いはモノマヌに可溶のものであ
る限り、䜿甚するこずは困難である。 䜆し、きらめき付䞎剀を含むビヒクル局以倖の
䞊䞋局のいづれか、或いは䞡方の暹脂には䜿甚の
制限はない。 液状暹脂に察するきらめき付䞎剀の添加量は、
液状暹脂の重量に察しお、通垞は0.1〜10重量
である。 きらめき付䞎剀は、予め液状暹脂ず混合しお䜿
甚されるが、塗料や印刷むンキに䜿甚する堎合は
液状暹脂を塗垃しおから撒垃しおもよい。 きらめき付䞎剀の添加量が0.1重量未満では、
本発明の効果が埗られず、10重量を超えるずも
はや増量による効果は認められない。 本発明の暹脂組成物は、塗料、印刷むンキ、泚
型品や繊維匷化プラスチツク成圢品等の成圢に甚
いられお、補品にきらめきのある矎麗な倖芳を䞎
える。䜆し、暹脂組成物を䞊蚘甚途に䟛し、きら
めきのある補品を埗る堎合にはきらめき付䞎剀を
構成する倚局プラスチツクフむルム现片が溶融す
るような高枩は避けなければならない。 次に、本発明の暹脂組成物を塗装、印刷むンキ
および成圢に甚いる堎合の態様を瀺す。 (1) 塗装 液状暹脂に盎接きらめき付䞎剀を混入しお塗装
するか、たたは、未也燥状態の塗膜にきらめき付
䞎剀を撒垃、固定し、その䞊に曎に䞊塗り塗装を
行う。 この堎合、きらめき付䞎剀ず䜵甚するビヒクル
は前述した条件を満足しなければならない。 䜕回も塗装する堎合は、きらめき付䞎剀混入局
以倖の塗膜を構成する暹脂に制限はない。 塗装方法は既存の各方法を甚いるこずができ
る。 (2) 印刷むンキ 印刷むンキのビヒクルに本発明の暹脂組成物を
甚いる限り、むンキの皮類、印刷の方法、被印刷
物の皮類に制限を加える必芁はなく、特に転写方
法により所望の結果を埗るこずができる。 (3) 成圢 泚型、繊維匷化プラスチツクFRPの成圢、
金型を甚いる加熱、加圧成圢のいづれもが実甚的
である。 泚型、䞊びに加熱、加圧成圢のいづれの堎合で
も、きらめき付䞎剀は、党䜓に混入しおもよく、
たた䞀郚分のみに混入しおもよい。 FRP成圢においおは衚面のゲルコヌト局が䞻
䜓ずなる。本発明の暹脂組成物を甚い、それぞれ
の手法により、補品に虹色のきらめきのある矎麗
な倖芳を䞎える堎合には、必芁に応じお暹脂組成
物に慣甚の添加剀、着色剀、補匷材等を䜵甚でき
るこずは勿論である。 本発明の暹脂組成物は、液状暹脂が前蚘(ã‚€)、
(ロ)、(ハ)の堎合には、それ自䜓を硬化させお成圢品
ずするこずができるが、玠材に本願発明の暹脂組
成物を適甚しお、玠材にきらめきのある矎麗な倖
芳を䞎えるこずもできる。 きらめき付䞎する玠材ずしおは、各皮セメント
補品、石こう補品、スレヌト、珪酞カルシりム
板、朚毛セメント板、炭酞マグネシりム板、合
板、ハヌドボヌド、チツプボヌド、繊維匷化プラ
スチツクス、各皮熱可塑性プラスチツク成圢品、
垃、玙、プラスチツクコンクリヌトなどがあげら
れる。 以䞋、実斜䟋によ぀お本発明をさらに詳しく説
明する。なお、実斜䟋䞭の郚はこずわりのない限
り重量郚を意味する。 実斜䟋  䞍飜和スピロアセタヌルずポリチオヌル化合物
の混合系に、光増感剀を加えた光硬化性暹脂昭
和高分子(æ ª)瀟補スピラツク―502100郚にアゟ
ビスむ゜ブチロニトリル0.3郚、きらめき付䞎剀
米囜MEADOWBROOK INVENTIONS瀟補、
商品名Crystaliner 322、ポリメチルメタクリ
レヌト屈折率1.48〜1.50ずポリ゚ステル屈
折率1.65の亀互倚局積局フむルムを玄0.3〜0.5
mm寞法にカツトしたもの郚を加えた。埗られ
た混合物を200mm×200mm×10mmの寞法に型取りし
たシリコンゎム型に、厚さが0.8〜mmになるよ
うに流し蟌んだ埌、10KWの出力をも぀玫倖線ラ
ンプ䞋20cmを20mm分の速床で通過させお䞀旊ゲ
ル化させた。 次いで、その䞊に䞍飜和ポリ゚ステル暹脂昭
和高分子(æ ª)瀟補、リゎラツク2004W100郚、
ガラス粉末日本硝子繊維(æ ª)瀟補、325メツシナ
100郚、チタン癜0.1郚、メチル゚チルケトンパヌ
オキシド郚、ナフテン酞コバルト0.5郚からな
る混合物を泚入し、宀枩で硬化させた埌、80℃で
時間埌硬化させた。 脱型埌、衚面の光硬化性暹脂局を再床50KWの
出力をも぀玫倖線照射装眮ランプ䞋20cmを
分の速床で通過させお埌硬化させた。 埗られた化粧板は、半透明䞋癜地に無数の虹色
のあるきらめきを呈し、頗る矎麗であり、オパヌ
ル調が再珟されおいた。 䞊蚘の方法においお、䞍飜和スピロアセタヌル
ずポリチオヌル化合物の混合系に光増感剀を加え
た光硬化性暹脂昭和高分子(æ ª)瀟補、スピラツク
―502の代りに、䞍飜和ポリ゚ステル暹脂
昭和高分子(æ ª)瀟補、リゎラツク2004Wを甚
いた堎合は、きらめき付䞎剀を同量添加しおも、
た぀たく効果がなく、単に黒぀ぜいゎミ様の浮遊
物が入぀おいるずしか芋えないものであ぀た。 実斜䟋  第図のごずき掗面化粧台のモデル型
1000mm、300mm、30mm、50mm、
100mm、コヌナヌ郚30Rに離型剀を塗垃し、ゲ
ルコヌトずしお゚ポキシ―アクリレヌト型ビニル
゚ステル暹脂昭和高分子(æ ª)瀟補、リポキシ―
820100郚、メチル゚チルケトンパヌオキシド
郚、ナフテン酞コバルト郚からなる混合物を
0.5〜0.7mm厚に塗装し、ゲル化させた。 次いで、ビスプノヌルに゚チレンオキシド
をモル付加させ、末端のアルコヌル性氎酞基を
アクリル゚ステル化したビニル゚ステル暹脂新
䞭村化孊(æ ª)瀟補、NK゚ステル、―BPE―
100郚に、実斜䟋ず同䞀のきらめき付䞎剀
Crystaliner 3220.3〜0.5mm寞法にカツトし
たもの郚、過酞化ベンゟむル郚、ゞメチル
アニリン0.2郚を加えた混合物を0.5〜mm皋床に
塗垃し垞枩で硬化させた。この際、空気に觊れた
面はゲル化状態で粘着性があ぀た。 サヌプヌスマツト30pを眮いお、裏打ち暹脂
ずしお䞍飜和ポリ゚ステル暹脂昭和高分子(æ ª)瀟
補、リゎラツク158BQTを100郚、黒色顔料
リゎラツクカラヌRC―81黒郚、メチル゚チ
ルケトンパヌオキシド郚からなる混合暹脂を塗
垃した。その埌、ガラスマツト450をプラむ
同䞀暹脂で積局した。 硬化埌、脱型し、端郚仕䞊げ、衚面研磚しお埗
られた掗面化粧台は、黒䞋地に無数の䞃色のキラ
メキを呈し頗る矎麗なものであ぀た。 実斜䟋  厚さ12mmで倧きさが450mm×450mmの耐氎合板
に、ポリ゚ステル暹脂昭和高分子(æ ª)瀟補、リゎ
ラツク1608C100郚、炭酞カルシりム100郚、
黒色顔料リゎラツクカラヌRC81黒10郚、メ
チル゚チルケトンパヌオキシド郚、ナフテン酞
コバルト郚からなる混合暹脂を玄mm厚に塗垃
し、硬化埌研磚した。 次いで、その䞊に光硬化型暹脂昭和高分子(æ ª)
瀟補、ビニル゚ステル暹脂、リポキシVR―77
50郚、トリメチロヌルプロパントリアクリレヌト
50郚、ベンゟプノン郚、ゞメチルアミノ゚タ
ノヌル郚からなる混合暹脂を0.7〜0.8mm厚にな
るように塗垃した。 厚さ50Όのポリ゚チレンテレフタレヌトフむル
ムに、䞍飜和スピロアセタヌルずポリチオヌル化
合物の混合系に光増感剀を加えた光硬化性暹脂
昭和高分子(æ ª)瀟補、スピラツク―502100郚、
実斜䟋で甚いたものず同䞀のきらめき付䞎剀
Crystaliner322郚、ベンゟプノン0.5郚
からなる混合暹脂でがたんの花暡様を描いた埌、
倪陜光に20分間晒しおむンキを硬化させた。 このがたんの花暡様を描いたポリ゚チレンテレ
フタレヌトフむルムを絵柄が䞊蚘した光硬化型暹
脂補塗膜に接するように密着させ、脱泡した埌、
50KWの出力をも぀玫倖線照射装眮䞋、20cmを
分の速床で通過させた。 硬化埌、フむルムを陀去するず、螺田様のきら
めきをも぀がたんの絵柄が塗膜に転写された。 次いで、アクリルラツカヌ昭和高分子(æ ª)瀟
補、ビニロヌル92Tを玄70Όになるように塗装
した。 也燥埌、バフ仕䞊げをするず、黒地に青〜赀色
にきらめく螺田調のがたんの絵柄の付された頗る
矎麗な化粧板が埗られた。 実斜䟋  600mm×600mmのアルミニりム補ハニカムサンド
むツチ板に、150Ό厚のシヌト王子油化(æ ª)瀟補、
合成玙ナポを、カルボキシメチルセルロヌズの
氎溶液を介しお密着させ、10mm角の長さが
600mmの鉄補角材を眮いお泚入甚の型を䜜成した。 これに、ポリビニルピロリドン郚、氎25郚、
メタノヌル70郚からなる溶液を30〜50Ό厚䜍にス
プレヌ塗装し、也燥しないうちに、きらめき付䞎
剀米囜MEARL CORPORATION瀟補、
Crystoliner 322の0.5〜ミリカツト0.7郚
ポリビニルピロリドンに察しおを郚分的に濃
淡を぀けお撒垃した。 塗膜也燥埌、α―石こう100郚、氎36郚、アク
リル゚マルゞペン昭和高分子(æ ª)瀟補、AP―
60410郚、黒色顔料山陜色玠(æ ª)瀟補、サンダ
むスヌパヌ10郚、セメント甚ガラス繊維1/4
むンチカツト郚からなる混合スラリヌを泚
入、硬化させた。 硬化埌脱型するず、黒色石こう衚面に、恰も銀
河のように無数のきらめきのある暡様の付された
成圢品が埗られた。 ゚ポキシ圓量187の液状゚ポキシ暹脂100郚に、
キシリレンゞアミン35郚を配合した混合物を暡様
の䞊に0.7〜0.8mm厚になるように刷毛で塗装し、
硬化させた。 研磚、バフ掛けしお埗られる塗装石こう板は、
黒色玠地に虹色の無数のきらめきがみられ、甚だ
矎しいものであ぀た。 この時、゚ポキシ圓量187の液状゚ポキシ暹脂
ずキシリレンゞアミンからなる混合物の代りに、
ポリ゚ステル暹脂、䞊びにスチレン含有ビニル゚
ステル暹脂を甚いた堎合は、きらめきが党く倱な
われ、幟分着色された暡様ずしか芋えず、比范に
ならないほど劣悪なものであ぀た。 実斜䟋  衚面を600の研磚玙で研磚埌、トリクレン掗
浄した300mm×300mm×mmのアルミニりム板に、
ビニル゚ステル暹脂昭和高分子(æ ª)瀟補、リポキ
シ―806DA100郚、黒色顔料リゎラツクカ
ラヌ黒、RC―81郚、メチル゚チルケトンパ
ヌオキシド郚、ナフテン酞コバルト郚をよく
混合しお玄0.7mm厚に塗装した埌、実斜䟋で甚
いたず同様のがたんの花柄を描いたポリ゚チレン
テレフタレヌトフむルムを密着、硬化させた。 硬化埌フむルムを陀去するず、黒䞋地にきらめ
きのある、がたんの花柄が転写されたアルミ板が
埗られた。 トツプコヌトずしお、䞍飜和スピロアセタヌル
暹脂昭和高分子(æ ª)瀟補、スピラツク―3155
を0.2mm厚になるように塗装した埌、30KWの出
力をも぀玫倖線照射装眮䞋20cmを、分の速
床で通過させお硬化させた。 埗られた化粧アルミ板は、䞋地がアルミ板ずい
぀た違いの他は、倖芳は実斜䟋の堎合ず異なら
ず、頗る矎麗なものであ぀た。 実斜䟋  盎埄100mmのガラス補シダヌレにシリコン暹脂
離型剀を塗垃した埌、次の配合物を泚入した。 光硬化性暹脂昭和高分子(æ ª)瀟補、スピラツク
―502 70郚 トリメチロヌルプロパントリアクリレヌト 30郚 ベンゟプノン 0.5〃 アゟビスむ゜ブチロニトリル 0.3〃 チタン癜 0.01〃 きらめき付䞎剀 MEARL CORPORATION補 Crystaliner 322 0.1〜0.3mmカツトタむプ 3″ 最初、30KWの玫倖線照射装眮䞋20cmを
分で通過硬化させた埌、80℃時間、100℃時
間で埌硬化させた。 衚面硬さが4Hの硬く半透明な、無数の䞃色の
きらめきをも぀た頗る矎麗なオパヌル様泚型品が
埗られた。泚型品は、ボタン、ペンダント、ネツ
クレス等に利甚可胜であ぀た。 実斜䟋  ゚ポキシ圓量187の液状゚ポキシ暹脂370郚ずス
ルフアミン120郚を80゜〜120℃の枩床で反応させ
お、融点70〜75℃の゚ポキシ暹脂プレポリマヌを
補造した。 このプレポリマヌ100郚に、―゚チル――
メチルむミダゟヌル0.5郚、きらめき付䞎剀実
斜䟋で甚いたものず同皮のもの郚、ステア
リン酞亜鉛郚、合成ワツクス系離型剀郚を配
合した埌、80〜90℃のロヌルで混緎、冷华しお
0.5〜mm䜍に粗砕した。 この粗砕物を金型枩床140〜150℃で、倖盎埄
145mm、内郚盎埄83mm、深さ30mmの同心円状の灰
皿の金型に入れ、灰皿を成圢した。 この時、成型枩床が170℃を越えるず、きらめ
きが消倱しおしたう傟向がみられた。 埗られた灰皿は、琥珀色の玠地に無数の虹色の
あるきらめきが付䞎され、甚だ矎しか぀た。
[Formula] An unsaturated (meth)acrylate oligomer having one or more of the following in one molecule. For example, polyester to (meth)acrylates, vinyl ester resin, spiroacetal to (meth)acrylates, urethane to (meth)acrylates, poly(meth)acrylates of polyhydric alcohols with a molecular weight of 200 or more, trishydroxyalkyl isocyan Nurate (meth)acrylate, polyether ~ (meth)acrylates, ether of unsaturated alcohol of methylolmelamine. As vinyl ester resin, epoxy~
(meth)acrylates and poly(meth)acrylates of alkylene oxide adducts of polyhydric phenols or novolaks. The above oligomers can be used in combination freely. Additionally, these oligomers may be used in combination with solvents or monomers that do not dissolve the multilayer plastic film strip. (b) A mixed use system of unsaturated spiroacetal or unsaturated cycloacetal containing two or more allyl ether type unsaturated bonds in one molecule and a polythiol compound. For example, a reaction resin of diarylidene pentaerythrite and tetrathioglycolate of pentaerythrite. (c) Epoxy resins using amines, amine adducts, or liquid polyamides as curing agents. High temperature curing using acid anhydrides is also available, but no particular advantage has been found and prolonged heating at high temperatures tends to impair the sparkle. The present invention consists of using a glitter-imparting agent together with a liquid resin that does not swell or dissolve the glitter-imparting agent, and the resin itself or The objective is to impart iridescent sparkle to the target material or molded product. If a solvent or liquid resin that dissolves the plastic film constituting the glitter-imparting agent is used as a vehicle, this glittering iridescence disappears completely, leaving behind an unattractive appearance that looks like dirt mixed in. For this purpose, aromatic hydrocarbons, esters,
The solvents normally used as vehicles, such as ketones, halogenated hydrocarbons, and nitroparaffins, and the monomers, such as styrene, methacrylates, acrylates, vinyl acetate, etc., are used depending on the type of plastic that makes up the film. Depending on the situation, it is generally not used as a vehicle. Therefore, resins, paints, inks, etc. that contain these solvents or monomers as one component should not be used in combination with glitter-imparting agents, as long as the polymer constituting the plastic film is soluble in these solvents or monomers. It is difficult. However, there are no restrictions on the use of resins in either or both of the upper and lower layers other than the vehicle layer containing the glitter-imparting agent. The amount of glitter-imparting agent added to the liquid resin is
Usually 0.1 to 10% by weight based on the weight of liquid resin
It is. The glitter-imparting agent is used by being mixed with a liquid resin in advance, but when used in paints or printing inks, the glitter-imparting agent may be sprayed after applying the liquid resin. If the amount of glitter-imparting agent added is less than 0.1% by weight,
The effect of the present invention cannot be obtained, and if the amount exceeds 10% by weight, no effect can be observed by increasing the amount. The resin composition of the present invention is used for molding paints, printing inks, cast products, fiber-reinforced plastic molded products, etc., and gives the products a sparkling and beautiful appearance. However, when using the resin composition for the above-mentioned purpose to obtain a product with glitter, it is necessary to avoid high temperatures that would melt the multilayer plastic film strips constituting the glitter-imparting agent. Next, embodiments in which the resin composition of the present invention is used for painting, printing ink, and molding will be shown. (1) Painting The glitter-imparting agent is mixed directly into the liquid resin and applied, or the glitter-imparting agent is sprinkled and fixed on the undried coating film, and then a top coat is applied on top. In this case, the vehicle used in combination with the glitter-imparting agent must satisfy the conditions mentioned above. In the case of multiple coatings, there is no restriction on the resin constituting the coating film other than the glitter-imparting agent-containing layer. As the coating method, existing methods can be used. (2) Printing ink As long as the resin composition of the present invention is used as a printing ink vehicle, there is no need to place any restrictions on the type of ink, printing method, or type of printing substrate, and in particular, it is possible to obtain the desired results by the transfer method. Can be done. (3) Molding Casting, molding of fiber reinforced plastic (FRP),
Both heating and pressure molding using a mold are practical. In any case of casting, heating, or pressure molding, the glitter-imparting agent may be mixed throughout.
Alternatively, it may be mixed only in a portion. In FRP molding, the gel coat layer on the surface is the main component. When using the resin composition of the present invention to give a product a beautiful appearance with iridescent sparkle using any of the methods, additives, colorants, reinforcing materials, etc. commonly used in the resin composition may be added as necessary. Of course, both can be used together. In the resin composition of the present invention, the liquid resin is the above (a),
In the cases of (b) and (c), the resin composition of the present invention can be cured to form a molded product, but the resin composition of the present invention can be applied to the material to give it a sparkling and beautiful appearance. You can also do that. Materials that give glitter include various cement products, gypsum products, slate, calcium silicate boards, wood wool cement boards, magnesium carbonate boards, plywood, hardboards, chipboards, fiber-reinforced plastics, various thermoplastic molded products,
Examples include cloth, paper, and plastic concrete. Hereinafter, the present invention will be explained in more detail with reference to Examples. In addition, parts in the examples mean parts by weight unless otherwise specified. Example 1 100 parts of a photocurable resin (Spirac T-502 manufactured by Showa Kobunshi Co., Ltd.) prepared by adding a photosensitizer to a mixed system of unsaturated spiroacetal and a polythiol compound and 0.3 parts of azobisisobutyronitrile Part, glitter-imparting agent (manufactured by MEADOWBROOK INVENTIONS, USA)
Product name Crystaliner #322, an alternating multi-layer laminated film of polymethyl methacrylate (refractive index 1.48-1.50) and polyester (refractive index 1.65) approximately 0.3-0.5
2 parts (cut into mm size) were added. The resulting mixture was poured into a silicone rubber mold with dimensions of 200 mm x 200 mm x 10 mm to a thickness of 0.8 to 1 mm, and then heated 20 cm under an ultraviolet lamp with an output of 10 KW at a speed of 20 mm/min. The mixture was allowed to pass through the gel to form a gel. Next, 100 parts of unsaturated polyester resin (manufactured by Showa Kobunshi Co., Ltd., Rigoratsuku #2004W) was added thereon,
Glass powder (manufactured by Nippon Glass Fiber Co., Ltd., 325 mesh)
A mixture consisting of 100 parts of titanium white, 0.1 parts of titanium white, 2 parts of methyl ethyl ketone peroxide, and 0.5 parts of cobalt naphthenate was injected and cured at room temperature, followed by post-curing at 80° C. for 4 hours. After demolding, the photocurable resin layer on the surface was reapplied 20cm/20cm under the lamp of an ultraviolet irradiation device with an output of 50KW.
Post-cure was carried out by passing at a speed of 100 min. The obtained decorative board exhibited countless iridescent sparkles on a translucent white background, was extremely beautiful, and reproduced an opal tone. In the above method, unsaturated polyester resin is used instead of a photocurable resin (Spirac T-502, manufactured by Showa Kobunshi Co., Ltd.), which is a mixture of unsaturated spiroacetal and polythiol compound with a photosensitizer added. (Showa Kobunshi Co., Ltd., Rigoratsuku #2004W), even if the same amount of glitter-imparting agent is added,
It had no brightening effect and looked like nothing more than black, dust-like floating matter. Example 2 A model model of a bathroom vanity as shown in Fig. 1 (a=
1000mm, b=300mm, c=30mm, d=50mm, e=
100mm, corner part 30R), apply a mold release agent and use epoxy-acrylate type vinyl ester resin (manufactured by Showa Kobunshi Co., Ltd., Lipoxy R-) as a gel coat.
820) 100 parts, methyl ethyl ketone peroxide 2
1 part of cobalt naphthenate.
It was painted to a thickness of 0.5 to 0.7 mm and gelled. Next, a vinyl ester resin (manufactured by Shin-Nakamura Chemical Co., Ltd., NK ester, A-BPE-4) was prepared by adding 2 moles of ethylene oxide to bisphenol A and converting the terminal alcoholic hydroxyl group into acrylic ester.
A mixture of 100 parts, 1 part of the same glittering agent as in Example 1 (Crystaliner #322, cut into 0.3-0.5 mm size), 2 parts of benzoyl peroxide, and 0.2 parts of dimethylaniline was added to about 0.5-1 mm. was applied and cured at room temperature. At this time, the surface exposed to air was in a gelatinous state and sticky. Place Surf Ace Mat 30p and add 100 parts of unsaturated polyester resin (manufactured by Showa Kobunshi Co., Ltd., Rigoratsuku 158BQT) as a backing resin, 5 parts of black pigment (Rigoratsuku Color RC-81 Black), and 2 parts of methyl ethyl ketone peroxide. A mixed resin was applied. Thereafter, 5 plies of glass mat #450 were laminated with the same resin. After curing, the mold was removed, the edges were finished, and the surface was polished.The resulting bathroom vanity was extremely beautiful, with a myriad of seven-colored glitter on the black base. Example 3 100 parts of polyester resin (manufactured by Showa Kobunshi Co., Ltd., Rigoratsuku #1608C), 100 parts of calcium carbonate,
A mixed resin consisting of 10 parts of black pigment (Rigorak Color RC81 Black), 2 parts of methyl ethyl ketone peroxide, and 1 part of cobalt naphthenate was applied to a thickness of approximately 1 mm, and after curing was polished. Next, a photocurable resin (Showa Kobunshi Co., Ltd.) is applied on top of it.
company, vinyl ester resin, lipoxy VR-77)
50 parts trimethylolpropane triacrylate
A mixed resin consisting of 50 parts of benzophenone, 1 part of dimethylaminoethanol, and 1 part of dimethylaminoethanol was applied to a thickness of 0.7 to 0.8 mm. 100 parts of a photocurable resin (manufactured by Showa Kobunshi Co., Ltd., Spirac T-502), which is a mixture of unsaturated spiroacetal and polythiol compounds and a photosensitizer added to a 50Ό thick polyethylene terephthalate film;
After drawing a peony flower pattern with a mixed resin consisting of 2 parts of the same glittering agent (Crystaliner #322) used in Example 1 and 0.5 parts of benzophenone,
The ink was cured by exposing it to sunlight for 20 minutes. A polyethylene terephthalate film with a peony flower pattern is placed in close contact with the above-mentioned photocurable resin coating, and after defoaming,
Under a UV irradiation device with an output of 50KW, 5 cm of 20cm
It was passed at a speed of m/min. After curing, when the film was removed, the sparkling peony design of Rata was transferred to the paint film. Next, an acrylic lacquer (manufactured by Showa Kobunshi Co., Ltd., Vinyroll 92T) was applied to a thickness of about 70Ό. After drying and buffing, a strikingly beautiful decorative board with a blue to red sparkling peony pattern on a black background was obtained. Example 4 A 150 Ό thick sheet (manufactured by Oji Yuka Co., Ltd.,
Synthetic paper (YUPO) was adhered with a 1% aqueous solution of carboxymethyl cellulose, and the length of 10 mm square was
A mold for injection was created by placing a 600mm square iron block. To this, 5 parts of polyvinylpyrrolidone, 25 parts of water,
Spray a solution of 70 parts of methanol to a thickness of 30 to 50 ÎŒm, and before it dries, apply a glittering agent (manufactured by MEARL CORPORATION, USA).
0.7 part (0.5-1 mm cut) of Crystoliner #322 (based on polyvinylpyrrolidone) was applied in partial shading. After drying the coating, add 100 parts of α-gypsum, 36 parts of water, acrylic emulsion (manufactured by Showa Kobunshi Co., Ltd., AP-
604) 10 parts, black pigment (manufactured by Sanyo Shiki Co., Ltd., Sandai Super), 10 parts, glass fiber for cement (1/4
A mixed slurry consisting of 5 parts (inch cut) was injected and cured. When the mold was removed after curing, a molded product with countless glittering patterns on the black gypsum surface, resembling galaxies, was obtained. 100 parts of liquid epoxy resin with an epoxy equivalent of 187,
A mixture containing 35 parts of xylylene diamine is applied onto the pattern with a brush to a thickness of 0.7 to 0.8 mm.
hardened. Painted gypsum boards obtained by polishing and buffing are
Countless rainbow-colored sparkles could be seen on the black background, making it extremely beautiful. At this time, instead of a mixture consisting of a liquid epoxy resin with an epoxy equivalent of 187 and xylylene diamine,
When a polyester resin or a styrene-containing vinyl ester resin was used, the glitter was completely lost and only a slightly colored pattern appeared, which was incomparably inferior. Example 5 A 300 mm x 300 mm x 3 mm aluminum plate whose surface had been polished with #600 abrasive paper and cleaned with trichlorethylene was
Thoroughly mix 100 parts of vinyl ester resin (manufactured by Showa Kobunshi Co., Ltd., Lipoxy R-806DA), 5 parts of black pigment (Rigorak Color Black, RC-81), 2 parts of methyl ethyl ketone peroxide, and 1 part of cobalt naphthenate. After coating to a thickness of approximately 0.7 mm, a polyethylene terephthalate film with a peony flower pattern similar to that used in Example 3 was adhered and hardened. After curing, the film was removed to obtain an aluminum plate with a glittering black background and a peony flower pattern transferred onto it. As a top coat, unsaturated spiroacetal resin (Spirac U-3155, manufactured by Showa Kobunshi Co., Ltd.)
After coating to a thickness of 0.2 mm, the coating was cured by passing 20 cm under an ultraviolet irradiation device with an output of 30 KW at a speed of 5 m/min. The appearance of the obtained decorative aluminum plate was the same as that of Example 3, except that the base was an aluminum plate, and was extremely beautiful. Example 6 After applying a silicone resin mold release agent to a glass shear dish having a diameter of 100 mm, the following formulation was injected. Photocurable resin (manufactured by Showa Kobunshi Co., Ltd., Spirak T-502) 70 parts trimethylolpropane triacrylate 30 parts benzophenone 0.5〃 Azobisisobutyronitrile 0.3〃 Titanium white 0.01〃 Sparkling agent Crystaliner manufactured by MEARL CORPORATION #322 0.1~0.3mm cut type 3″ Initially, 20cm below the 30KW ultraviolet irradiation device for 5m/
After pass-curing for 1 minute, post-curing was carried out at 80°C for 4 hours and at 100°C for 2 hours. A beautiful opal-like cast product with a surface hardness of 4H, which is hard and translucent, and has countless seven-colored sparkles was obtained. Cast products could be used for buttons, pendants, net dress, etc. Example 7 370 parts of a liquid epoxy resin having an epoxy equivalent weight of 187 and 120 parts of sulfamine were reacted at a temperature of 80° to 120°C to produce an epoxy resin prepolymer having a melting point of 70 to 75°C. To 100 parts of this prepolymer, 2-ethyl-4-
After blending 0.5 parts of methylimidazole, 3 parts of a glittering agent (same type as used in Example 6), 3 parts of zinc stearate, and 1 part of a synthetic wax-based mold release agent, it was rolled at 80 to 90°C. Knead and cool
It was coarsely crushed to about 0.5 to 1 mm. This coarsely crushed material is molded at a mold temperature of 140 to 150℃, and the outer diameter is
It was placed in a concentric ashtray mold with a diameter of 145 mm, an internal diameter of 83 mm, and a depth of 30 mm to form an ashtray. At this time, when the molding temperature exceeded 170°C, there was a tendency for the glitter to disappear. The resulting ashtray had an amber base with countless iridescent sparkles and was extremely beautiful.

【図面の簡単な説明】[Brief explanation of drawings]

第図は、実斜䟋で䜿甚した掗面化粧台のモ
デル型の斜芖図である。
FIG. 1 is a perspective view of a model of the bathroom vanity used in Example 2.

Claims (1)

【特蚱請求の範囲】  屈折率の異なる少なくずも皮の透明なプラ
スチツクフむルムが亀互に10局以䞊積局された倚
局プラスチツクフむルム现片ず、該倚局プラスチ
ツクフむルム现片を膚最ないし溶解しない䞋蚘の
硬化可胜な液状暹脂の少なくずも皮ずからなる
暹脂組成物。 (ã‚€) モノマヌ類の䜵甚なしに硬化する、アクリロ
むル基たたはメタクリロむル基を分子䞭に
個以䞊有する䞍飜和メタアクリレヌト系オ
リゎマヌ。 (ロ) 䞍飜和スピロアセタヌル、或いはアリル゚ヌ
テル型䞍飜和結合を分子䞭に個以䞊有する
䞍飜和シクロアセタヌルずポリチオヌル化合物
ずの混合物。 (ハ) アミン類、アミン付加物たたは液状ポリアミ
ドを硬化剀ずする゚ポキシ暹脂。
[Scope of Claims] 1. A multilayer plastic film strip in which ten or more layers of at least two kinds of transparent plastic films having different refractive indexes are alternately laminated, and a curable film that does not swell or dissolve the multilayer plastic film strip. A resin composition comprising at least one type of liquid resin. (b) Contains one acryloyl group or methacryloyl group in one molecule, which cures without the use of monomers.
An unsaturated (meth)acrylate oligomer having 1 or more unsaturated (meth)acrylate oligomers. (b) A mixture of an unsaturated spiroacetal or an unsaturated cycloacetal having two or more allyl ether type unsaturated bonds in one molecule and a polythiol compound. (c) Epoxy resins using amines, amine adducts, or liquid polyamides as curing agents.
JP57132155A 1982-07-30 1982-07-30 Resin composition Granted JPS5922746A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57132155A JPS5922746A (en) 1982-07-30 1982-07-30 Resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57132155A JPS5922746A (en) 1982-07-30 1982-07-30 Resin composition

Publications (2)

Publication Number Publication Date
JPS5922746A JPS5922746A (en) 1984-02-06
JPS6338069B2 true JPS6338069B2 (en) 1988-07-28

Family

ID=15074643

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57132155A Granted JPS5922746A (en) 1982-07-30 1982-07-30 Resin composition

Country Status (1)

Country Link
JP (1) JPS5922746A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1064521C (en) * 1997-04-20 2001-04-18 蒋措净 Sweet potato foodstuff
US6291056B1 (en) * 1998-07-01 2001-09-18 Engelhard Corporation Flakes from multilayer iridescent films for use in paints and coatings

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5423693A (en) * 1977-07-22 1979-02-22 Kureha Chem Ind Co Ltd Preparation of vinylidene chloride-vinyl chloride copolymer
JPS5582137A (en) * 1978-12-16 1980-06-20 Takayoshi Kimura Aqueous composition of platy substance

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5423693A (en) * 1977-07-22 1979-02-22 Kureha Chem Ind Co Ltd Preparation of vinylidene chloride-vinyl chloride copolymer
JPS5582137A (en) * 1978-12-16 1980-06-20 Takayoshi Kimura Aqueous composition of platy substance

Also Published As

Publication number Publication date
JPS5922746A (en) 1984-02-06

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