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JPS6234781B2 - - Google Patents
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JPS6234781B2 - - Google Patents

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Publication number
JPS6234781B2
JPS6234781B2 JP6136578A JP6136578A JPS6234781B2 JP S6234781 B2 JPS6234781 B2 JP S6234781B2 JP 6136578 A JP6136578 A JP 6136578A JP 6136578 A JP6136578 A JP 6136578A JP S6234781 B2 JPS6234781 B2 JP S6234781B2
Authority
JP
Japan
Prior art keywords
weather
resistant polymer
ethylene
sheet
component
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
JP6136578A
Other languages
Japanese (ja)
Other versions
JPS54153854A (en
Inventor
Toshio Honda
Yukio Fukura
Hikari Ishikawa
Shozo Kojima
Itsuo Tanuma
Masao Ogawa
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.)
Bridgestone Corp
Original Assignee
Bridgestone Corp
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 Bridgestone Corp filed Critical Bridgestone Corp
Priority to JP6136578A priority Critical patent/JPS54153854A/en
Publication of JPS54153854A publication Critical patent/JPS54153854A/en
Publication of JPS6234781B2 publication Critical patent/JPS6234781B2/ja
Granted legal-status Critical Current

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  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)

Description

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

本発明は接着性良奜な耐候性ポリマヌシヌトに
関するものである。 ポリ゚チレン、ポリプロピレン等の耐候性、特
に耐オゟン劣化性の良奜なポリマヌは数倚く存圚
するが、これらのポリマヌに共通の欠点は、耐候
性ポリマヌを䞻成分ずする材料を互に、あるいは
他の材料ず接着するこずが困難なこずである。埓
来これらのポリマヌからなる各皮の材料の接着性
を改善するためにコロナ攟電、バフ等の衚面凊理
が行われおいるが、これらの手段は繁雑な割には
効果が少ないので䞀般にすすめられる方法ずは蚀
い難い。埓぀お耐候性ポリマヌは接着操䜜を必芁
ずしないか、あるいはさほど接着匷床を芁しない
特定の分野にのみ甚いられおおり、耐候性を必芁
ずする分野における曎に広範囲な利甚を可胜にす
るために接着性を改善するこずが望たれおいた。 本発明は䞊蚘の背景をもずに、接着性が良奜で
か぀耐候性の良いポリマヌ組成物から成るシヌト
を提䟛するこずを目的ずする。 すなわち本発明は耐候性ポリマヌず第二成分ず
しおの−ポリブタゞ゚ン暹脂を必須成分ず
し、䞊蚘耐候性ポリマヌず第二成分の比率が80
20〜1090の重量比の範囲ずしお成るシヌトの衚
面がハロゲン分子又は擬ハロゲン化合物で凊理さ
れおいるこずを特城ずする接着性良奜な耐候性ポ
リマヌ組成物に係る。 本発明の組成物に甚いる第䞀成分である耐候性
ポリマヌは、ポリ゚チレン、ポリプロピレン、゚
チレン−酢酞ビニル共重合䜓、゚チレン−プロピ
レン共重合䜓、゚チレン−アクリル酞共重合䜓、
゚チレン−アクリル酞共重合䜓の金属むオン架橋
物、ポリむ゜ブチレン等、䞻鎖に実質的に二重結
合を含たない単䞀重合䜓および共重合䜓を含む他
に、゚チレン−プロピレン−非共圹ゞ゚ン重合䜓
やむ゜ブチレン−む゜プレン共重合䜓のように少
量、通垞重量以䞋の䞍飜和結合を䞻鎖に有す
る共重合䜓を含む。重量より倚くの䞍飜和結
合を䞻鎖に有するポリマヌは耐候性が䜎䞋するの
で甚いられない。 次に本発明の組成物に甚いる第二成分ずしおの
䞻鎖に䞍飜和結合を含たずか぀偎鎖に䞍飜和基を
有する−ポリブタゞ゚ンは、組成物の耐候
性を損わずに接着性を向䞊させる目的に第䞀成分
ずブレンドされるものである。䞊蚘の劂く第二成
分は䞻鎖に䞍飜和結合を含たないので耐オゟン劣
化性はかなり良奜であり、か぀偎鎖に䞍飜和基を
有するため接着性を改善するための衚面凊理を行
うこずが可胜である。第二成分ずしお他に望たし
い条件は、前蚘耐候性ポリマヌず盞溶性が良いこ
ずおよびすぐれた機械的性質を有しおいるこずで
ある。このような理由から、第二成分ずしお、
−ポリブタゞ゚ンずりわけ内郚に結晶領域
を有し、抗匵力の高いシンゞオタクチツク
−ポリブタゞ゚ンが奜んで甚いられる。 第二成分は、前蚘耐候性ポリマヌず第二成分の
和を100ずした堎合、少なくずも20重量以䞊加
えないず接着性の向䞊には寄䞎しない。接着性の
改善には第二成分は倚いほど奜たしく、特に30重
量以䞊でその効果は顕著にある。これはある䞀
定以䞊の第二成分を加えた堎合、ブレンド物の衚
面に第二成分の偎鎖の䞍飜和基が接着に十分な量
珟れるこずによるものである。䞀方第二成分が倚
くなりすぎるず組成物の硬床が増し、柔軟性が倱
われ、か぀玫倖線に察する劣化が目立぀ようにな
るので、第二成分は90重量、奜たしくは70を
越えない範囲で加えられる。 䞊蚘耐候性ポリマヌず第二成分をブレンドし成
圢したシヌトの衚面は、凊理剀、すなわちハロゲ
ン分子又は擬ハロゲン化合物ハロゲノむドで
凊理するこずが接着性胜をさらに向䞊させる䞊で
必芁である。本発明で甚いられるハロゲン分子ず
しおは、塩玠、臭玠、ペり玠及びそれらの0.1〜
20重量濃床の氎溶液たたは有機溶媒溶液などの
他に、次亜塩玠酞や次亜臭玠酞の氎溶液のように
酞の存圚䞋でハロゲン分子を発生する化合物を含
む。 たた擬ハロゲン化合物ハロゲノむドずしお
は、ハロゲン化む゜シアナヌト、−モノハロア
ルキルりレタン、−ゞハロアルキルりレタ
ン、−ゞハロアリルスルホンアミド、ハロ
ゲン化硫黄、スルプニルハラむド、ハロメチル
゚ヌテル、チオシアノゲン、沃化アゞド、臭化ア
ゞド、塩化沃玠、臭化沃玠、トリクロロアセテむ
ツクアシツドアむオダむド、アセテむツクアシツ
ドブロマむド、硝酞沃玠、アルキルハむポハラむ
ド、アルキルチオニルクロラむド、アリルチオニ
ルクロラむド、塩化ニトロシル、臭化ニトロシ
ル、ハロゲン化む゜シアヌル酞、ハロゲン化メチ
ルヒダントむン等が挙げられる。 䞊蚘した凊理剀の䞭でも性胜、凊理加工性、安
党性の点で擬ハロゲン化合物、特にハロゲン化む
゜シアナヌト、−ゞハロアルキルりレタ
ン、−ゞハロアリルスルホンアミド、アル
キルハむポハラむド、ハロゲン化む゜シアヌル
酞、ハロゲン化メチルヒダントむンが奜適に䜿甚
される。具䜓的には沃化む゜シアナヌト、
−ゞクロロ゚チルりレタン、−ゞブロモ゚
チルりレタン、−ゞクロロプロピルりレタ
ン、−ゞブロモプロピルりレタン、
−ゞクロロベンゞルりレタン、−ゞブロモ
ベンゞルりレタン、−ゞクロロトル゚ンス
ルホンアミド、−ゞブロモトル゚ンスルホ
ンアミド、第玚ブチルハむポクロラむド、トリ
クロロむ゜シアヌル酞、ゞクロロむ゜シアヌル
酞、ゞブロモゞメチルヒダントむン、ゞクロロメ
チルヒダントむンなどの化合物である。 䞊蚘擬ハロゲン化合物ハロゲノむドは、実
際の凊理に際しおはこれを適圓な溶媒に溶解し
0.1〜20重量、奜たしくは〜15重量の濃床
で甚いる。 本発明における䞊蚘凊理剀を有機溶媒溶液ずし
お甚いる堎合の溶媒の具䜓䟋ずしおは、四塩化炭
玠、クロロホルム、ゞクロロメタンなどのハロゲ
ン化炭化氎玠、ベンれン、ニトロベンれン、ハロ
ゲン化ベンれン、トル゚ン、キシレンなどの芳銙
族炭化氎玠、ゞメチル゚ヌテル、ゞ゚チル゚ヌテ
ル、テトラヒドロフランTHF、ゞオキサンな
どの鎖状或いは環状゚ヌテル、酢酞゚チルなどの
゚ステル類、ペンタン、ヘキサン、ヘプタン、オ
クタン、シクロヘキサンなどの脂肪族炭化氎玠、
アセトン、シクロヘキサノン、メチル゚チルケト
ンMEKなどのケトン類、゚タノヌル、゚チ
レングリコヌル、第玚ブチルアルコヌルなどの
アルコヌル類などを挙げるこずができ、䞭でもテ
トラヒドロフランTHF、ゞオキサン、アセト
ン、ベンれン、トル゚ン、四塩化炭玠、クロロホ
ルム、メチル゚チルケトンMEK、酢酞゚チ
ル、゚タノヌルが奜たしく甚いられる。 前蚘凊理剀でシヌトを凊理する方法ずしおは、
筆、刷毛による塗垃、スプレむ、浞挬など、シヌ
ト衚面ず前蚘凊理剀を接觊させるこずが可胜ない
かなる工業的手段も採甚するこずができる。 䞊蚘した凊理剀により凊理された本発明のシヌ
トの衚面は、平滑面を保぀おおり、倖芳では凊理
前のものず区別が぀かない。組成物の性胜も凊理
の前埌で党く倉わりはない。 この凊理されたシヌトに察する接着性は凊理埌
幎以䞊経過しおも䜎䞋するこずはない。たた奜
適䟋においおは、凊理されたシヌト衚面郚分の汚
損防止のためフむルム、ガムテヌプなどで被芆保
護するこずにより接着性胜は曎に良奜に保存され
るこずになる。 尚前蚘組成物には、カヌボンブラツク、シリ
カ、炭酞カルシりム、珪酞カルシりム、リグニン
等の充填剀、鉱物油、怍物油、合成可塑剀等の軟
化剀等を配合しおおくこずは勿論可胜である。た
た所芁に応じお組成物に硫黄、過酞化物、キノむ
ド等の加硫剀及び加硫助剀等を配合し、成圢、加
硫しおシヌトずし、次いで前蚘の衚面凊理を行う
こずもできる。さらには本発明の組成物に金属、
有機繊維、ガラス繊維等の芯材、あるいは補匷材
を埋め蟌んで䜿甚するこずもできる。 本発明の衚面凊理によ぀お埗られた耐候性ポリ
マヌず第二成分からなるシヌトは、埓来の耐候性
ポリマヌの性質を損うこずなく、接着性が著しく
改善されたもので、被着䜓ずしお本発明のシヌト
自身の他に金属、ゎム、プラスチツク、朚、ガラ
ス等ず接続するのに甚いられ、特に防氎シヌト、
ガスケツト、ベルト等の接合郚の接着に極めお効
果的である。 尚本発明のシヌトず被着䜓を接着するには通垞
ポリりレタン暹脂、゚ポキシ暹脂、プノヌルア
ルデヒド暹脂、倚䟡プノヌルアルデヒド暹脂、
ニトリル系ゎムセメント等を接着衚面に介圚させ
お圧着するこずにより行われる。 以䞋に本発明を実斜䟋により曎に詳现に説明す
る。 実斜䟋  䞋蚘第衚に瀺すように、゚チレン−プロピレ
ン−゚チリデンノルボネン共重合䜓日本合成ゎ
ム補、JSREP33、ペり玠䟡26、以䞋EPDMず蚘
すに皮々の量のシンゞオタクテむツク−
ポリブタゞ゚ン日本合成ゎム補、JSR
RB820、以䞋PBず蚘すをブレンドした加硫ゎ
ムの物性ず接着性胜を評䟡した。基本配合は、
EPDMずPBの合蚈量100重量郚に察し、HAFブラ
ツク50、プロセスオむル、ステアリン酞
−む゜プロピル−N′−プニル−−プニレ
ンゞアミン、パラフむンワツクス、タツキフ
アむダヌずしおロゞン、亜鉛華、硫黄、
−オキシゞ゚チレン−−ベンゟチアゟヌルスル
プンアミド各重量郚であり、加硫条件は160
℃で20分間である。 接着性の評䟡は次のようにしお行぀た。 幅60mm×長さ150mm×厚さmmの加硫ゎムシヌ
トを枚甚意し接着面に重量のN′−ゞ
クロロ−−トル゚ンスルホンアミドを含むアセ
トン溶液をはけで塗垃し衚面凊理を行぀た。凊理
面に接着剀ずしおアゞプレン−213デナポン
瀟補、−NCO含有量9.4100郚に察し、硬化剀
のMOCA3′−ゞクロロ−4′−ゞアミノ
ゞプニルメタン、デナポン瀟補25gをアセト
ン125gに溶解したものず混合し接着剀ずした。
このりレタン溶液を加硫ゎム凊理前に塗垃し、也
燥埌枚のゎムシヌトを貌り合わせ圧着ロヌラで
圧着し、宀枩で24時間攟眮埌、むンチカツタヌで
打抜いたものを接着詊隓片ずした。 これずは別に同様の方法で衚面凊理した枚の
加硫ゎムシヌトの間に厚さmmの熱可塑性りレタ
ン暹脂日本ポリりレタン補、DN4818シヌト
を挟み蟌みアむロンで200℃で40秒間圧着し、溶
融接着させたものを同様にむンチカツタヌで打
抜き接着詊隓片ずした。 各詊隓片を匕匵り詊隓機により50mm分の速床
で字剥離詊隓を行぀た。埗た結果を添付図面に
瀺す。尚図面䞭曲線は詊隓片、曲線は詊隓
片の倫々の結果を瀺す。 たた加硫ゎムの耐候性の怜蚎を行぀た。耐オゟ
ン劣化詊隓は加硫ゎムの倧きさは幅20mm、長さ70
mm、厚みmmのシヌトを40䌞長させ、枩床40
℃、オゟン濃床90ppHm条件䞋で168時間劣化さ
せた埌のクラツクの発生状況を調べた。たた耐玫
倖線劣化詊隓は、加硫ゎム厚みmmをJIS3号
のダンベルで打抜き、その詊隓片を400W氎銀燈
䞋距離15cm玄19000Όを眮き、時間玫倖
線を照射させた埌、匕匵速床300mmで枬定し、最
初のものず比范しお䜎䞋率を算出した。 䞊蚘詊隓結果を次の第衚に䜵蚘する。
The present invention relates to a weather-resistant polymer sheet with good adhesion. There are many polymers such as polyethylene and polypropylene that have good weather resistance, especially resistance to ozone deterioration, but a common drawback of these polymers is that they cannot be used together or with other materials. It is difficult to adhere. Conventionally, surface treatments such as corona discharge and buffing have been performed to improve the adhesion of various materials made of these polymers, but these methods are complicated and have little effect, so they are not generally recommended methods. It's hard to say. Therefore, weather-resistant polymers are used only in specific areas that do not require adhesive operations or do not require significant adhesive strength, and are used in adhesive applications to enable more widespread use in areas that require weather resistance. It was hoped to improve sexuality. Based on the above background, the present invention aims to provide a sheet made of a polymer composition that has good adhesiveness and good weather resistance. That is, the present invention has a weather-resistant polymer and a 1,2-polybutadiene resin as the second component as essential components, and the ratio of the weather-resistant polymer to the second component is 80:
The present invention relates to a weather-resistant polymer composition with good adhesion, characterized in that the surface of the sheet is treated with a halogen molecule or a pseudohalogen compound in a weight ratio of 20 to 10:90. The weather-resistant polymer that is the first component used in the composition of the present invention includes polyethylene, polypropylene, ethylene-vinyl acetate copolymer, ethylene-propylene copolymer, ethylene-acrylic acid copolymer,
In addition to single polymers and copolymers that do not substantially contain double bonds in the main chain, such as metal ion crosslinked ethylene-acrylic acid copolymers and polyisobutylene, ethylene-propylene-nonconjugated diene polymers It also includes copolymers having a small amount, usually 3% by weight or less, of unsaturated bonds in the main chain, such as isobutylene-isoprene copolymers. Polymers having more than 3% by weight of unsaturated bonds in the main chain are not used because their weather resistance decreases. Next, 1,2-polybutadiene, which is used as a second component in the composition of the present invention and does not contain an unsaturated bond in its main chain and has an unsaturated group in its side chain, can adhere without impairing the weather resistance of the composition. It is blended with the first component for the purpose of improving properties. As mentioned above, the second component does not contain unsaturated bonds in its main chain, so it has fairly good ozone deterioration resistance, and since it has unsaturated groups in its side chains, it can be surface-treated to improve adhesion. It is possible. Other desirable conditions for the second component are that it has good compatibility with the weather-resistant polymer and excellent mechanical properties. For this reason, as the second component,
1,2-polybutadiene, especially syndiotactic 1,2 which has an internal crystalline region and has high tensile strength.
-Polybutadiene is preferably used. The second component does not contribute to improving adhesion unless it is added in an amount of at least 20% by weight, where the sum of the weather-resistant polymer and the second component is 100. In order to improve adhesion, it is preferable to have a larger amount of the second component, and the effect is particularly noticeable when it is 30% by weight or more. This is because when a certain amount or more of the second component is added, unsaturated groups in the side chains of the second component appear on the surface of the blend in an amount sufficient for adhesion. On the other hand, if the amount of the second component is too large, the hardness of the composition will increase, flexibility will be lost, and deterioration due to ultraviolet light will become noticeable. Added. In order to further improve adhesive performance, the surface of the sheet formed by blending the weather-resistant polymer and the second component must be treated with a treatment agent, that is, a halogen molecule or a pseudohalogen compound (halogenoid). The halogen molecules used in the present invention include chlorine, bromine, iodine, and their 0.1 to
In addition to a 20% concentration aqueous solution or organic solvent solution, it includes a compound that generates halogen molecules in the presence of an acid, such as an aqueous solution of hypochlorous acid or hypobromous acid. Examples of pseudohalogen compounds (halogenoids) include halogenated isocyanates, N-monohaloalkyl urethanes, N,N-dihaloalkyl urethanes, N,N-dihaloallylsulfonamides, sulfur halides, sulfenyl halides, and halomethyl Ether, thiocyanogen, azide iodide, azide bromide, iodine chloride, iodine bromide, trichloroacetate iodide, acetate bromide, iodine nitrate, alkyl hypohalide, alkylthionyl chloride, allylthionyl chloride, nitrosyl chloride , nitrosyl bromide, halogenated isocyanuric acid, halogenated methylhydantoin, and the like. Among the above-mentioned processing agents, pseudohalogen compounds, especially halogenated isocyanates, N,N-dihaloalkyl urethanes, N,N-dihaloallylsulfonamides, alkyl hypohalides, and halogen Preferred are halogenated isocyanuric acid and halogenated methylhydantoin. Specifically, iodized isocyanate, N,N
-dichloroethyl urethane, N,N-dibromoethyl urethane, N,N-dichloropropylurethane, N,N-dibromopropylurethane, N,N
-dichlorobenzyl urethane, N,N-dibromobenzyl urethane, N,N-dichlorotoluenesulfonamide, N,N-dibromotoluenesulfonamide, tertiary butylhypochloride, trichloroisocyanuric acid, dichloroisocyanuric acid, dibromodimethylhydantoin, Compounds such as dichloromethylhydantoin. The above pseudohalogen compounds (halogenoids) must be dissolved in an appropriate solvent during actual processing.
It is used in concentrations of 0.1 to 20% by weight, preferably 1 to 15% by weight. Specific examples of solvents when the above treatment agent in the present invention is used as an organic solvent solution include carbon tetrachloride, chloroform, halogenated hydrocarbons such as dichloromethane, benzene, nitrobenzene, halogenated benzene, toluene, aromatic hydrocarbons such as xylene, etc. Hydrocarbons, chain or cyclic ethers such as dimethyl ether, diethyl ether, tetrahydrofuran (THF), and dioxane, esters such as ethyl acetate, aliphatic hydrocarbons such as pentane, hexane, heptane, octane, and cyclohexane,
Examples include ketones such as acetone, cyclohexanone, and methyl ethyl ketone (MEK); alcohols such as ethanol, ethylene glycol, and tertiary butyl alcohol; among others, tetrahydrofuran (THF), dioxane, acetone, benzene, toluene, and tetrachloride. Carbon, chloroform, methyl ethyl ketone (MEK), ethyl acetate, and ethanol are preferably used. The method of treating the sheet with the treatment agent is as follows:
Any industrial means capable of bringing the treatment agent into contact with the sheet surface can be employed, such as application with a brush or brush, spraying, or dipping. The surface of the sheet of the present invention treated with the above-mentioned treatment agent maintains a smooth surface and is indistinguishable from the sheet before treatment in appearance. The performance of the composition also remains unchanged before and after treatment. Adhesion to this treated sheet does not deteriorate even after one year or more after treatment. Further, in a preferred embodiment, the adhesive performance is better preserved by covering and protecting the treated sheet surface with a film, gummed tape, etc. to prevent staining. It is of course possible to incorporate fillers such as carbon black, silica, calcium carbonate, calcium silicate, and lignin, and softeners such as mineral oil, vegetable oil, and synthetic plasticizers into the composition. Further, if necessary, a vulcanizing agent such as sulfur, peroxide, quinoid, vulcanizing aid, etc. may be added to the composition, and the sheet may be formed by molding and vulcanizing, and then subjected to the above-mentioned surface treatment. Furthermore, the composition of the present invention may include a metal,
It is also possible to use a core material such as organic fiber or glass fiber, or a reinforcing material embedded therein. The sheet made of the weather-resistant polymer and the second component obtained by the surface treatment of the present invention has significantly improved adhesion without impairing the properties of conventional weather-resistant polymers, and can be used as an adherend. In addition to the sheet of the present invention, it can be used to connect with metal, rubber, plastic, wood, glass, etc., and in particular, a waterproof sheet,
Extremely effective for bonding joints of gaskets, belts, etc. In order to bond the sheet of the present invention and the adherend, polyurethane resin, epoxy resin, phenolaldehyde resin, polyhydric phenolaldehyde resin,
This is done by interposing nitrile rubber cement or the like on the adhesion surface and compressing it. The present invention will be explained in more detail below using examples. Example 1 As shown in Table 1 below, various amounts of syndiotactic 1 were added to ethylene-propylene-ethylidene norbornene copolymer (manufactured by Japan Synthetic Rubber Co., Ltd., JSREP33, iodine value 26, hereinafter referred to as EPDM). ,2-
Polybutadiene (Japan Synthetic Rubber, JSR
The physical properties and adhesive performance of a vulcanized rubber blended with RB820 (hereinafter referred to as PB) were evaluated. The basic composition is
For a total of 100 parts by weight of EPDM and PB, HAF Black 50, process oil 5, stearic acid 2, N
-isopropyl-N'-phenyl-p-phenylenediamine 1, paraffin wax 1, rosin 2 as a tackifier, zinc white 5, sulfur 2, N
-oxydiethylene-2-benzothiazolesulfenamide 1 part by weight, and the vulcanization conditions were 160
℃ for 20 minutes. Adhesion was evaluated as follows. Prepare two vulcanized rubber sheets 60 mm wide x 150 mm long x 2 mm thick, and apply an acetone solution containing 5% by weight N,N'-dichloro-p-toluenesulfonamide to the adhesive surface with a brush. I processed it. Add 100 parts of Adiprene L-213 (manufactured by DuPont, -NCO content 9.4%) as an adhesive to the treated surface, and add MOCA (3,3'-dichloro-4,4'-diaminodiphenylmethane, Dupont) as a hardening agent. (manufactured by S.A.) was dissolved in 125 g of acetone and mixed to make an adhesive.
This urethane solution was applied before the vulcanized rubber treatment, and after drying, the two rubber sheets were bonded together using a pressure roller, left at room temperature for 24 hours, and then punched out using an inch cutter to obtain an adhesive test piece A. Separately, a sheet of thermoplastic urethane resin (DN4818, manufactured by Nippon Polyurethane) with a thickness of 1 mm was sandwiched between two vulcanized rubber sheets whose surface had been treated in the same manner, and the sheet was pressed with an iron at 200°C for 40 seconds. , and the melt-adhesive pieces were similarly punched out using an inch cutter B to obtain an adhesive test piece B. Each test piece was subjected to a T-peel test using a tensile tester at a speed of 50 mm/min. The results obtained are shown in the attached drawings. In the drawings, curve 1 shows the results for test piece A, and curve 2 shows the results for test piece B. We also investigated the weather resistance of vulcanized rubber. In the ozone deterioration resistance test, the size of the vulcanized rubber was 20 mm in width and 70 mm in length.
mm, 2 mm thick sheet was stretched by 40% and the temperature was 40
The occurrence of cracks was investigated after deterioration for 168 hours at ℃ and ozone concentration of 90 ppHm. In addition, in the ultraviolet ray deterioration test, vulcanized rubber (thickness 2 mm) was punched out with a JIS No. 3 dumbbell, the test piece was placed under a 400 W mercury lamp at a distance of 15 cm (approximately 19,000 ÎŒW), and after being irradiated with ultraviolet rays for 8 hours, the tensile speed was set at 30 mm. The rate of decrease was calculated by comparing it with the first one. The above test results are also listed in Table 1 below.

【衚】 実斜䟋  䞋蚘第衚に瀺すように、む゜プレン−む゜プ
チレンゎム日本合成ゎム補IIR−268、以䞋IIR
ず蚘すに皮々の量のPBをブレンドした加硫ゎ
ムの物性ず接着性胜を評䟡した。 基本配合はIIRずPBの合蚈量100重量郚に察し
HAFブラツク50、プロセスオむル、ステアリ
ン酞、−む゜プロピル−N′−プニル−
−プニレンゞアミン、パラフむンワツクス
、ロゞン、亜鉛華、硫黄、−オキシ゚
チレン−−ベンゟチアゟヌルスルプンアミド
、テトラメチレンチりラム−モノスルフむド
0.5各重量郚であり、加硫時間は160℃で20分間で
あ぀た。加硫物の物性は匕匵り物性および耐オゟ
ン劣化の評䟡を行぀た。 たた接着評䟡は実斜䟋ず同様に、加硫衚面を
重量のN′−ゞクロロ−−トル゚ンス
ルホンアミドを含むアセトン溶液を塗垃し、衚面
凊理を行぀た埌に、50重量のアゞプレン−
213MOCA10025のアセトン溶液の接着
剀を塗垃し、枚を貌り合せ宀枩で攟眮しお硬化
させたものを詊隓片ずした。詊隓結果を第衚
に瀺す。
[Table] Example 2 As shown in Table 2 below, isoprene-isoptylene rubber (IIR-268 manufactured by Nippon Synthetic Rubber, hereinafter referred to as IIR)
The physical properties and adhesive performance of vulcanized rubber blended with various amounts of PB were evaluated. The basic composition is based on the total amount of IIR and PB of 100 parts by weight.
HAF black 50, process oil 5, stearic acid 2, N-isopropyl-N'-phenyl-p
-Phenylenediamine 1, paraffin wax 1, rosin 2, zinc white 5, sulfur 2, N-oxyethylene-2-benzothiazolesulfenamide 1, tetramethylenethiuram monosulfide
0.5 parts by weight each, and the vulcanization time was 20 minutes at 160°C. The physical properties of the vulcanizate were evaluated for tensile properties and ozone deterioration resistance. For adhesion evaluation, as in Example 1, an acetone solution containing 5% by weight N,N'-dichloro-p-toluenesulfonamide was applied to the vulcanized surface, and after surface treatment, 50% by weight of N,N'-dichloro-p-toluenesulfonamide was applied to the vulcanized surface. Adiprene L-
Test piece C was prepared by applying an adhesive of an acetone solution of 213/MOCA (100/25), bonding the two sheets together, and leaving them at room temperature to harden. The test results are shown in Table 2.

【衚】 実斜䟋  第衚に瀺すように、䜎密床ポリ゚チレンナ
カロンMS30、䞉菱油化補、以䞋LD−PEず蚘
すず皮々の量のPBを高枩120℃ロヌルで混
合ブレンドし、150℃のプレスで溶融成圢したシ
ヌトの物性及び接着性を評䟡した。接着方法は実
斜䟋ず同様に行い、埗た詊隓片をずした。詊
隓結果を第衚に䜵蚘する。
[Table] Example 3 As shown in Table 3, low density polyethylene (Yukalon MS30, manufactured by Mitsubishi Yuka, hereinafter referred to as LD-PE) and various amounts of PB were mixed and blended using a high temperature (120°C) roll. The physical properties and adhesive properties of sheets melt-molded in a press at 150°C were evaluated. The adhesion method was carried out in the same manner as in Example 1, and the obtained test piece was designated as D. The test results are also listed in Table 3.

【衚】 実斜䟋  第衚に瀺す様に、゚チレン、アクリル酞共重
合䜓の金属むオン架橋物であるサヌリン1555
Naむオンタむプ、䞉井ポリケミカル補、以䞋サ
ヌリンず蚘すず皮々の量のPBを高枩ロヌルで
混合し、枩床150℃のプレスにお溶融成圢したシ
ヌトの物性及び接着性を実斜䟋ず同様にしお評
䟡した。接着方法は実斜䟋ず同様に行い、埗た
詊料を詊隓片ずした。詊隓結果を第衚に瀺
す。
[Table] Example 4 As shown in Table 4, Surlyn 1555 is a metal ion crosslinked product of ethylene and acrylic acid copolymer.
(Na ion type, made by Mitsui Polychemicals, hereinafter referred to as Surlyn) and various amounts of PB were mixed in a high temperature roll and melt-formed in a press at a temperature of 150°C. The physical properties and adhesive properties of the sheet were the same as in Example 1. It was evaluated as follows. The adhesion method was carried out in the same manner as in Example 1, and the obtained sample was designated as Test Piece E. The test results are shown in Table 4.

【衚】 実斜䟋  EPDMずPBをブレンドした加硫ゎムシヌトず
金属鉄片の接着を行぀た。実斜䟋の実隓番
号1dEPDHPB7030で補䜜した加硫シ
ヌトを重量のDCTSのアセトン溶液で衚面凊
理を行぀た。 䞀方鉄SS41衚面をシペツトプラスト凊理
した埌、アセトンで掗浄し、次いで金属ず泚型り
レタンの接着剀であるケムロツク218米囜、ヒ
ナヌリンケミカル瀟補を刷毛塗りした。 接着剀ずしおアゞプレン−213MOCA
10025の50重量のアセトン溶液を甚い凊理
した加硫ゎムおよび金属面に刷毛で塗垃を斜し、
溶剀が蒞発した埌䞡者を貌り合せセロテヌプで固
定し、そのたた宀枩に48時間攟眮し、硬化接着さ
せた。その接着片を実斜䟋ず同様に、匕匵速床
50mm秒で180°剥離を行い、接着力を評䟡した
結果、75Kg25mmの接着力で加硫ゎムの凝集砎壊
をおこした。この結果、耐候性の優れた加硫シヌ
トで保護された金属の耇合䜓が埗られた。
[Table] Example 5 A vulcanized rubber sheet made of a blend of EPDM and PB was bonded to a metal (iron piece). The vulcanized sheet produced in Experiment No. 1d (EPDH/PB=70/30) of Example 1 was surface-treated with a 5% by weight DCTS acetone solution. On the other hand, after the iron (SS41) surface was subjected to shotplast treatment, it was cleaned with acetone, and then Chemlock 218 (manufactured by Huurin Chemical Co., USA), which is an adhesive between metal and cast urethane, was applied with a brush. Adiprene L-213/MOCA as adhesive
(100/25) was applied with a brush to the treated vulcanized rubber and metal surfaces using a 50% by weight acetone solution.
After the solvent had evaporated, the two pieces were pasted together and fixed with cellophane tape, and left at room temperature for 48 hours to cure and bond. The adhesive piece was pulled at the same speed as in Example 1.
Peeling was performed at 180° at 50 mm/sec and the adhesive strength was evaluated. As a result, cohesive failure of the vulcanized rubber occurred at an adhesive strength of 75 kg/25 mm. As a result, a metal composite protected by a vulcanized sheet with excellent weather resistance was obtained.

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

添付図面は実斜䟋の詊隓片およびの
EPDMPBブレンド比率ず剥離力ずの関係を瀺
す曲線図である。
The attached drawings show test pieces A and B of Example 1.
It is a curve diagram showing the relationship between EPDM/PB blend ratio and peeling force.

Claims (1)

【特蚱請求の範囲】  耐候性ポリマヌず第二成分の−ポリブ
タゞ゚ン暹脂を必須成分ずし、䞊蚘耐候性ポリマ
ヌず第二成分の比率が8020〜1090の重量比の
範囲ずしお成る組成物から成圢したシヌトの衚面
がハロゲン分子又は擬ハロゲン化合物で凊理され
おいるこずを特城ずする接着性良奜な耐候性ポリ
マヌシヌト。  前蚘耐候性ポリマヌが䞻鎖に䞍飜和結合を含
たないか、あるいは重量以䞋の䞍飜和結合を
有する特蚱請求の範囲第項蚘茉の接着性良奜な
耐候性ポリマヌシヌト。  耐候性ポリマヌがポリ゚チレン、ポリプロピ
レン、゚チレン−酢酞ビニル共重合䜓、゚チレン
−プロピレン共重合䜓、゚チレン−アクリル酞共
重合䜓、゚チレン−アクリル酞共重合䜓、゚チレ
ン−アクリル酞共重合䜓の金属むオン架橋物、ポ
リむ゜ブチレン、゚チレン−プロピレン−非共圹
ゞ゚ン共重合䜓、む゜ブチレン−む゜プレン共重
合䜓から遞ばれた少なくずも皮である特蚱請求
の範囲第項たたは第項蚘茉の接着性良奜な耐
項性ポリマヌシヌト。  耐候性ポリマヌず第二成分が重量比で7030
〜3070の範囲にある特蚱請求の範囲第項、第
項たたは第項蚘茉の接着性良奜な耐候性ポリ
マヌシヌト。  第二成分がシンゞオタクテむツク−ポ
リブタゞ゚ン暹脂である特蚱請求の範囲第〜
項のいずれか䞀぀の項に蚘茉の接着性良奜な耐候
性ポリマヌシヌト。
[Claims] 1. A weather-resistant polymer and a second component, 1,2-polybutadiene resin, are essential components, and the weight ratio of the weather-resistant polymer and the second component is in the range of 80:20 to 10:90. 1. A weather-resistant polymer sheet with good adhesion, characterized in that the surface of the sheet molded from a composition comprising the above-mentioned composition is treated with a halogen molecule or a pseudohalogen compound. 2. The weather-resistant polymer sheet with good adhesion according to claim 1, wherein the weather-resistant polymer does not contain unsaturated bonds in its main chain or has 3% by weight or less of unsaturated bonds. 3 The weather-resistant polymer is polyethylene, polypropylene, ethylene-vinyl acetate copolymer, ethylene-propylene copolymer, ethylene-acrylic acid copolymer, ethylene-acrylic acid copolymer, metal ion of ethylene-acrylic acid copolymer A crosslinked product having good adhesive properties and durability according to claim 1 or 2, which is at least one selected from crosslinked products, polyisobutylene, ethylene-propylene-nonconjugated diene copolymers, and isobutylene-isoprene copolymers. Polymer sheet. 4 Weather-resistant polymer and second component in weight ratio of 70:30
A weather-resistant polymer sheet with good adhesion according to claim 1, 2 or 3, which has a ratio of 1 to 30:70. 5 Claims 1 to 4 in which the second component is a syndiotactic 1,2-polybutadiene resin
A weather-resistant polymer sheet with good adhesion as described in any one of the above items.
JP6136578A 1978-05-23 1978-05-23 Weather-resistant polymer composition having high adhesivity Granted JPS54153854A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6136578A JPS54153854A (en) 1978-05-23 1978-05-23 Weather-resistant polymer composition having high adhesivity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6136578A JPS54153854A (en) 1978-05-23 1978-05-23 Weather-resistant polymer composition having high adhesivity

Publications (2)

Publication Number Publication Date
JPS54153854A JPS54153854A (en) 1979-12-04
JPS6234781B2 true JPS6234781B2 (en) 1987-07-29

Family

ID=13169054

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6136578A Granted JPS54153854A (en) 1978-05-23 1978-05-23 Weather-resistant polymer composition having high adhesivity

Country Status (1)

Country Link
JP (1) JPS54153854A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4371662A (en) 1980-09-01 1983-02-01 Idemitsu Petrochemical Co., Ltd. Three-component resin compositions having improved coating properties
JPS5847048A (en) * 1981-09-14 1983-03-18 Takiron Co Ltd Cushioning material for use in transportation
US5153262A (en) * 1991-03-29 1992-10-06 The Goodyear Tire & Rubber Company Controlled morphology barrier elastomers made from blends of syndiotactic 1,2-polybutadiene and ethylene-vinyl acetate-vinyl alcohol terpolymers
US5091467A (en) * 1991-03-29 1992-02-25 The Goodyear Tire & Rubber Company Controlled morphology barrier elastomers made from blends of syndiotactic 1,2-polybutadiene and ethylene-vinyl acetate-vinyl alcohol terpolymers

Also Published As

Publication number Publication date
JPS54153854A (en) 1979-12-04

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