JPH0528265B2 - - Google Patents
Info
- Publication number
- JPH0528265B2 JPH0528265B2 JP60257675A JP25767585A JPH0528265B2 JP H0528265 B2 JPH0528265 B2 JP H0528265B2 JP 60257675 A JP60257675 A JP 60257675A JP 25767585 A JP25767585 A JP 25767585A JP H0528265 B2 JPH0528265 B2 JP H0528265B2
- Authority
- JP
- Japan
- Prior art keywords
- polyethylene
- composition
- polyisobutylene
- modified
- weight
- 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
- 239000000203 mixture Substances 0.000 claims description 62
- -1 polyethylene Polymers 0.000 claims description 55
- 229920000573 polyethylene Polymers 0.000 claims description 50
- 239000004698 Polyethylene Substances 0.000 claims description 48
- 229920002367 Polyisobutene Polymers 0.000 claims description 31
- 229920001903 high density polyethylene Polymers 0.000 claims description 29
- 239000004700 high-density polyethylene Substances 0.000 claims description 29
- 229920000092 linear low density polyethylene Polymers 0.000 claims description 26
- 239000004707 linear low-density polyethylene Substances 0.000 claims description 25
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 18
- 230000001070 adhesive effect Effects 0.000 claims description 13
- 239000000853 adhesive Substances 0.000 claims description 12
- 239000000155 melt Substances 0.000 claims description 2
- 239000002184 metal Substances 0.000 description 33
- 229910052751 metal Inorganic materials 0.000 description 33
- 229910000831 Steel Inorganic materials 0.000 description 18
- 229920005989 resin Polymers 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- 239000010959 steel Substances 0.000 description 18
- 238000000576 coating method Methods 0.000 description 14
- 239000011248 coating agent Substances 0.000 description 13
- 229920005992 thermoplastic resin Polymers 0.000 description 13
- 238000000034 method Methods 0.000 description 12
- 238000002844 melting Methods 0.000 description 11
- 230000008018 melting Effects 0.000 description 11
- 150000002739 metals Chemical class 0.000 description 10
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000005977 Ethylene Substances 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 238000010030 laminating Methods 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 229920003051 synthetic elastomer Polymers 0.000 description 5
- 239000005061 synthetic rubber Substances 0.000 description 5
- 239000004711 α-olefin Substances 0.000 description 5
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005554 pickling Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 229920002978 Vinylon Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 229920001179 medium density polyethylene Polymers 0.000 description 2
- 239000004701 medium-density polyethylene Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 239000011135 tin Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- ZWVMLYRJXORSEP-LURJTMIESA-N (2s)-hexane-1,2,6-triol Chemical compound OCCCC[C@H](O)CO ZWVMLYRJXORSEP-LURJTMIESA-N 0.000 description 1
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- BLDFSDCBQJUWFG-UHFFFAOYSA-N 2-(methylamino)-1,2-diphenylethanol Chemical compound C=1C=CC=CC=1C(NC)C(O)C1=CC=CC=C1 BLDFSDCBQJUWFG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 239000004805 Cyclohexane-1,2-dicarboxylic acid Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- MUBKMWFYVHYZAI-UHFFFAOYSA-N [Al].[Cu].[Zn] Chemical compound [Al].[Cu].[Zn] MUBKMWFYVHYZAI-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- WXCZUWHSJWOTRV-UHFFFAOYSA-N but-1-ene;ethene Chemical compound C=C.CCC=C WXCZUWHSJWOTRV-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 239000012969 di-tertiary-butyl peroxide Substances 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000012934 organic peroxide initiator Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
Description
産業上の利用分野
本発明は、変性ポリエチレン組成物に関する。
従来の技術
従来、金属の耐食性、外観、食品衛生上の改善
等のために金属管の内外面、金属板、電線ケーブ
ル、鋼線等にポリエチンレンを被覆したり、ある
いは各種合成樹脂のもつ欠点を改善するためにポ
リエチレンとの貼り合せによる複合物が知られて
いる。この場合のポリエチレンとしては、金属及
び各種合成樹脂との接着性を改良するために、ポ
リエチレンに不飽和カルボン酸もしくはその誘導
体で変性して接着性を付与した変性ポリエチレン
と合成ゴムとの組成物が知られている。
例えば、不飽和カルボン酸もしくはその誘導体
をグラフトした特定のメルトインデツクス比の実
質的に中低圧法エチレン重合体の変性エチレン重
合体と炭化水素系合成ゴムとからなる組成物（特
開昭56−120750号公報）、エポキシ樹脂系接着剤
を塗布して加熱処理した金属体に、特定のエチレ
ン・α−オレフインランダム共重合体を添加した
不飽和カルボン酸またはその無水物で変性したポ
リエチレンを加熱接着する方法（特開昭58−
168628号公報）、変性ポリエチレン及びポリイソ
ブチレンとからなるシートを介して金属箔と貼合
せた積層板（特開昭56−93541号公報）、変性高密
度ポリエチレン、エチレンとα−オレフインとの
共重合体及び必要に応じてゴム状重合体を配合し
たポリエチレン組成物とポリアミドとの多層積層
構造物（特開昭55−121058号公報）等が提案され
ている。一方、金属及び熱可塑性樹脂とポリエチ
レンとの接着性およびその耐久性を改良するもの
として、特定の線状低密度ポリエチレンを不飽和
カルボン酸もしくはその誘導体で変性したポリエ
チレンと合成ゴムとの組成物（特開昭57−165413
号公報）及び特定の線状低密度ポリエチンレンと
合成ゴムとの混合物に不飽和カルボン酸もしくは
その誘導体を反応させて変性した組成物（特開昭
57−165469号公報）も提案されている。
発明が解決しようとする問題点
上記の提案の組成物および方法における金属及
び熱可塑性樹脂等の被着体とポリエチレンとの接
着強度は改良されてはいるものの、被着体の低い
予熱温度における接着性については十分ではなか
つた。すなわち、変性ポリエチレンまたはその組
成物は、その樹脂の融点以上で被着体にねれない
と十分な接着性が発現しない。そのため、通常は
被着体を樹脂の溶融温度近くに予熱しておき、そ
の表面に溶融樹脂を被覆する。しかしながら、金
属体を複数回にわたつて被覆する場合、例えば鋼
管の内面及び外面を被覆する場合は、先に内面を
被覆した鋼管を樹脂の融点近くに予熱すると、既
に被覆した面が軟化して傷付や剥離したりするた
めに、鋼管の予熱温度をより低下させても接着が
可能な樹脂が必要であつた。また、被着体の予熱
温度を低くできない場合には、被覆後の冷却速度
を遅くすることにより被覆するため、ライン速度
（生産速度）が低下するという問題があつた。
この被着体の予熱温度を従来より低下させた場
合においても十分な接着性を有するものとして、
本発明者らは先に、特定のメルトインデツクスを
有する線状低密度ポリエチレンと変性物とポリイ
ソブチレンからなる変性ポリエチレン組成物（特
願昭60−99621号）提案した。
しかしながら、この組成物は、その予熱温度を
低下させた場合においても十分に接着性を有する
ものの、接着させた冷却後の機械的強度、例えば
鋼管被覆に用いた場合に、管端のネジ切りあるい
は配管時のパイプレンチ締めにより受けるトルク
に対する実用上の強度に改良の余地が残されてい
た。
本発明は、上記のような問題点を解消し、従来
のものに比べて被着体の予熱温度をより低下させ
た場合においても優れた接着性を有し、かつ実用
上の機械的強度を有する接着性ポリエチレン組成
物を提供することを目的とする。
問題点を解決するための手段
本発明者らは、上記の問題点を解消するために
鋭意検討を行つた結果、特定範囲のメルトインデ
ツクス（以下MIという）の線状低密度ポリエチ
レン変性物、ポリイソブチレン及び／又はその変
性物、及び高密度ポリエチンレンとからなる組成
物が本発明の目的を達成することを見出し本発明
を完成した。
すなわち、本発明は(A)MI7〜50ｇ／10分の線状
低密度ポリエチレンに、不飽和カルボン酸もしく
はその誘導体を反応させてなる変性ポリエチレン
10〜90重量％、(B)未変性ポリエチルンエン（但
し、高密度ポリエチレンを除く）０〜85重量％、
(C)高密度ポリエチレン及び／又は該高密度ポリエ
チレンに不飽和カルボン酸もしくはその誘導体を
反応させてなる変性高密度ポリエチレン５〜50重
量％及び(D)ポリイソブチレン及び／又は該ポリイ
ソブチレンに不飽和カルボン酸もしくはその誘導
体を反応させてなる変性ポリイソブチレン５〜50
重量％とからなる接着性ポリエチレン組成物を要
旨とする。
本発明において用いるMI7〜50ｇ／10分の線状
低密度ポリエチレン（以下LLDPEという）は、
クロム系またはチーグラー系の触媒の存在下に、
低圧の気相法、溶液法または液相法でエチレンと
α−オレフイン、例えばブテン−１、ペンテン−
１、ヘキサン−１、４−メチルペンテン−１、ヘ
プテン−１、オクテン−１等から選択されるもの
と共重合させて製造したもので、MIが７〜50
ｇ／10分、望ましくは８〜20ｇ／10分のものであ
る。ここでα−オレフインは一般には３〜20重量
％の割合で含まれる。これらLLDPEのうちでは、
低圧気相法で重合した密度が0.905〜0.950ｇ／
cm3、重量平均分子量ｗ／数平均分子量ｎが３
〜12のものが望ましい。上記LLDPEのMIが７
ｇ／10分未満では被着体の低い予熱温度における
接着性が不十分であり、一方50ｇ／10分を越える
場合は樹脂の強度が不十分となる。また、MI7〜
50ｇ／10分のLLDPE以外のポリエチレンでは、
被着体との接着性及びその耐久性が十分でない。
本発明で用いる未変性ポリエチレン（但し、高
密度ポリエチレンを除く）は、エチレンの単独重
合体又は共重合体で、望ましくは密度0.910〜
0.940ｇ／cm3及びMI0.1〜50ｇ／10分のものがあげ
られる。例えば、線状低密度ポリエチレン（以下
LLDPEという）、低密度ポリエチレン（以下
LDPEという）、中密度ポリエチレン（以下
MDPEという）、またはエチレン含量が50重量％
以上でありエチレンとα−オレフインもしくはビ
ニル単量体との共重合体などがあげられる。
本発明で用いる高密度ポリエチレン（以下
HDPEという）は、周知のごとく中低圧法で重合
して得られる密度0.941〜0.970ｇ／cm3のポリエチ
レンで、MI0.1〜50ｇ／10分、好ましくは１〜20
ｇ／10分のものである。このHDPEの特定量を配
合することにより接着性を低下させることなく機
械的強度を向上することができる。
本発明で用いるポリイソブチレンは、市販のも
のが使用できるが、ムーニー粘度（Ml1+4、100
℃、JIS Ｋ−6300以下同じ）が10〜150で、結晶
化度（Ｘ線回折法）が30％以下のものが好まし
い。また、ポリイソブチレン以外の合成ゴムでは
被着体との接着性が十分でない。
本発明に用いられる不飽和カルボン酸として
は、例えばアクリル酸、メタクリル酸、マレイン
酸、フマル酸、イタコン酸、シトラコン酸、エン
ド−ビ−シクロ〔２，２，１〕−１，４，５，６，
７，７−ヘキサシクロロ−５−ヘプテン−２，３
−ジカルボン酸、エンド−ビ−シクロ−〔２，２，
１〕−５−ヘプテン−２，３−ジカルボン酸、シ
ス−４−シクロヘキサン−１，２−ジカルボン酸
等があげられる。又、不飽和カルボン酸の誘導体
としては、酸無水物、エステルがあげられ、例え
ば無水マレイ酸、無水シトラコン酸、エンド−ビ
−シクロ−〔２，２，１〕−１，４，５，６，７，
７−ヘキサクロロ−５−ヘプテン−２，３無水ジ
カルボン酸、エンド−ビ−シクロ−〔２，２，１〕
−５−ヘプテン−２，３−無水ジカルボン酸、シ
ス−４−シクロヘキセン−１，２−無水ジカボン
酸、アクリル酸メチル、メタクリル酸メチル、ア
クリル酸エチル、メタクリル酸エチル、アクリル
酸ブチル、メタクリル酸ブチル、マレイン酸エス
テル（モノエステル、ジエステル）等があげられ
る。
LLDPE、HDPE又はポリイソブチレンに不飽
和カルボン酸又はその誘導体を反応させる方法は
公知の各種の方法を採用できる。例えば、
LLDPE、HDPE、又はポリイソルブチレンと不
飽和カルボン酸又はその誘導体を溶媒の存在下ま
たは不存在下で有機過酸化物の反応開始剤、例え
ば、ジタ−シヤリ−ブチルパーオキサイド、ジク
ミルパ−オキサイド、ベンゾイル−オキサイド、
２，５−ジメチル−２，５−ジ−（ターシヤリ−
ブチルペルオキシ）−ヘキシン−３、２，５−ジ
メチル−２，５−ジ−（ターシヤリ−ブチルペル
オキシ）−ヘキサン等を添加し、ヘンシエルミキ
サー、リボンブレンダー等の混合機で予め混合
し、この混合物をバンバリーミキサー、単軸又は
多軸の押出機でポリエチレン又はポリイソブチレ
ンの融点以上280℃以下の温度で溶融混練する。
又は、LLDPE、HDPE又はポリイソブイレンを
溶剤中に溶解し、その溶液中に不飽和カルボン酸
又はその誘導体と反応開始剤を添加して反応させ
てもよい。
ここでLLDPE、HDPE又はポリイソブチレン
に付加する不飽和カルボン酸又はその誘導体の量
は0.01〜３重量％が好ましい。従つて、不飽和カ
ルボン酸又はその誘導体及び有機過酸化物の反応
開始剤の添加量は、未変性LLDPE、HDPE又は
ポリイソブチレンの100重量部に対して不飽和カ
ルボン酸又はその誘導体0.05〜５重量部、反応開
始剤0.001〜0.5重量が好ましい。なお、得られる
変性ポリエチレン又は変性ポリイソブチレン中の
不飽和カルボン酸又はその誘導体の含有量が0.01
重量％未満では本発明効果の強靭な接着力が得ら
れず、一方３重量％を越える場合は接着力の増大
はみられず、ゲル状物の発生や着色等が増大し経
済的にも不利である。
次に、本発明の接着性ポリエチレン組成物は、
変性ポリエチレン10〜90重量％、望ましくは20〜
50重量％、未変性ポリエチレン（但し、HDPEを
除く）０〜85重量％、望ましくは０〜70重量％、
HDPE及び／又は変性HDPE5〜50重量％、望ま
しくは５〜40重量％、及びポリイソブチレン及
び／又は変性ポリイソブチレン５〜50重量％、望
ましくは５〜40重量％とからなる。変性ポリエチ
レン、未変性ポリエチレン及びポリイソブチレン
及び／又は変性ポリイソブチレンの含有量が上記
の範囲を外れる場合は、予熱温度の低い被着材に
対する接着性が不十分である。又HDPEの含有量
が５重量％未満では機械的強度が不十分であり、
一方50重量％を越えると予熱温度の低い被着材に
対する接着性が不十分となり共に本発明の目的を
達し得ない。
本発明の組成物は製造は、変性LLDPEとポリ
イソブチレン及び／又は変性ポリイソブチレン、
さらにはこれらと未変性ポリエチレンとを前記の
配合割合で混合することによつて得られる。上記
の各成分を均等に分散させて好物性をもつた組成
物にするには、例えば予めヘンシエルミキサー、
リボブレンダー、等で予備混合し、この混合物を
バンバリーミキサー、ロール、押出機等で組成物
の融点以上から280℃以下の温度で溶融混練する
方法が望ましい。なお、ポリイソブチレンがベー
ル状の場合は、バンバリーミキサー、ロール等で
加熱溶融混練する方法が望ましい。
また、本発明の組成物は、LLDPE、HDPE及
びポリイソブチレンとの前記配合割合の混合物
に、不飽和カルボン酸もしくはその誘導体を反応
させたものであつてもよい。さらには、この変性
混合物に、未変性ポリエチンレン、HDPE及び／
又は未変性ポリイソブチレンを前記の配合割合と
なるように混合してもよい。
本発明の組成物は、種々の添加剤、例えば、熱
安定剤、紫外線吸収剤、核剤、帯電防止剤、着色
剤等や種々の充填剤、例えば無機充填剤、可塑剤
等を配合することができる。これら添加剤等は、
組成物の調製時に、又は調製後に混合してもよ
い。
次に、本発明の変性ポリエチレン組成物は、金
属または熱可塑性樹脂と好適な積層物を形成する
ことができる。
本発明の変性ポリエチレン組成物を用いた積層
物における金属としては、鉄、アルミニウム、
銅、亜鉛、ニツケル、錫、ステンレス、真ちゆ
う、ブリキ、トタン等で板状、箔、筒状、管状、
線あるいはその他の形状をしたのものがあげられ
る。又、熱可塑性樹脂としては、ナイロン６、ナ
イロン66、ナイロン11、ナイロン12、ナイロン６
−10等のポリアミト、ポリエチレン、ポリプロピ
レン、ポリブテン等のオレフイン単独重合体又は
これらの共重合体等のポリオレフイン、ポリビニ
ルエアルコールを部分的にアセタール化した樹脂
（ビニロン）、エチレン−酢酸ビニル共重合体を部
分的に加水分解した樹脂（エバール）、ポリエチ
レンテレフタレートやポリブチレンテレフタレー
ト等のポリエステル、ポリ塩化ビニル等があげら
れるが、特にナイロン、ビニロンが好ましい。
本発明の変性ポリエチレン組成物を用いる積層
物は、本発明の変性ポリエチレン組成と前記と金
属又は熱可塑性樹脂から選択されるものとを積層
することによつて得られる。
積層物を得る方法は特に限定されるものではな
く、例えばそれぞれをフイルム、シート状として
おき熱圧着する方法、ダイ外部でラミネートする
方法、ダイ内部でラミネート（共押出）する方
法、チユーブ状またはシート状に押出コーテイン
グする方法あるいは粉体塗装する方法等の公知の
方法を利用することができる。なお、金属との積
層においては、通常溶剤脱脂、酸洗、シヨツトブ
ラスト、リン酸亜鉛処理、リン酸カルシウム等の
前処理が行われ、さらにプライマー処理としてエ
ポキシ系樹脂のプライマーを介することにより、
より強靭な接着力を有する積層物を得ることがで
きる。エポキシ系樹脂のプライマーとしては、一
液性又は二液性の変性エポキシ系樹脂プライマー
が耐熱性あるいは安定性の点から好ましい。
本発明の変性ポリエチレン組成物を用いる積層
物の構造は、本発明の変性ポリエチレン組成物と
前記の金属又は熱可塑性樹脂から選択されるもの
と積層する２層構造を基本とするが、必要に応じ
て種々の組合せを行うことができる。例えば、変
性ポリエチレン組成物（以下該組成物という）／
金属、該組成物／熱可塑性樹脂、該組成物／金
属／該組成物、金属／該組成物／金属、金属／該
組成物／熱可塑性樹脂、熱可塑性樹脂／該組成
物／熱可塑性樹脂等の組合せで、さらに、これら
を組合せることや他の物質、例えば繊維、紙、木
板等を組合せることもできる。
本発明の該組成物は、上記のように金属又は熱
可塑性樹脂と好適な複合物（被覆、積層等）を形
成するが、特に金属管の被覆に有用であるので、
以下に樹脂被覆金属管の製造例について説明す
る。
基材の金属管は、シヨツトプラスト、グリツド
プラスト又は酸洗い等の表面処理を行い清浄にす
る。さらにこの上にプライマー処理としてエポキ
シ系接着剤等を塗布することがより強靭な接着力
を有する樹脂層を得るために望ましい。前処理を
施した金属管は、高周波誘導加熱等により所望の
温度、例えば100℃以上、好ましくは110〜150℃
に加熱し、この金属管外面に該組成物を融点以
上、好ましくは200〜230℃の温度でチユーブ状に
押出し又はシート状に巻き付けて被覆する。被覆
の厚さは目的により異なるが通常は0.3mm程度で
ある。さらに、その上に外装材、例えばポリオレ
フイン、好ましくは高密度ポリエチレンを融点以
上、好ましくは200〜230℃の温度でチユーブ状に
押出し又はシート状に巻き付け被覆後、直ちに水
冷する。外装材の厚さは通常２mm程度である。な
お、外装材の被覆は用途に応じて適宜省略しても
よい。
また、上記の金属管被覆を金属管の内外両面に
ついて行う場合は、前処理を施した金属管を100
〜150℃に加熱し、その内面に該組成物及びポリ
オレフイン、好ましくはポリエチレンの順に粉体
塗装を施して樹脂層を形成させる。次いで、この
内面被覆金属管を、100℃〜内面被覆樹脂の融点
未満の温度に加熱し、この金属管外面に上記と同
様に該組成物及びポリオレフインを被覆する。
発明の効果
本発明の該組成物は、既に提案されている変性
ポリエチレン組成物に比べ、金属及び熱可塑性樹
脂等の被着体の予熱温度をより低下させた場合か
ら高い温度に到るまで優れた接着力を示す。この
ため樹脂の多層被覆において、既被覆層の軟化や
溶融による不都合がなく、また被覆後の冷却速度
を遅くする必要がないために生産速度を低下させ
ることがない。
又、本発明の組成物は、従来のものに比べて接
着後の機械的強度が向上するため、例えば被覆鋼
管において耐ネジ切り性、耐パイプレンチトルク
性等の実用上に十分な強度を有する。
本発明の該組成物は、上記のような優れた特性
により、金属や熱可塑性樹脂との複合化、特に多
層の複合化に好適である。複合化の例としては、
鋼管や鋳鉄管の内外面、鋼板、金属箔、電線ケー
ブル、鋼線等の被覆あるいはタンクのライニン
グ、又は各種熱可塑性樹脂その多層のフイルム、
シート、ボトル、容器等の積層物があげられる。
実施例
次に、実施例をあげて本発明を詳細に説明す
る。なお、実施例における部および％はすべて重
量基準で、試験方法は次の通りである。
(1) MI
ASTM Ｄ−1238E（190℃、2160ｇ）
(2) 剥離強度
酸洗処理鋼板（SS−41）100×100×0.3mmを
電解脱脂した後、加熱板上で所定温度に予熱
し、この上に本発明の該組成物のシート（厚１
mm）／高密度ポリエチレン（厚さ３mm）のシー
トを220℃に加熱し溶融して融着し、10秒間放
置後に流水中に浸漬して冷却して試験片を作成
した。試験片の樹脂層を巾10mmに切断して一部
剥離してつかみ代とし、インストロン引張試験
機を用い剥離速度50mm／分で90°剥離強度を23
℃及び50℃で測定した。
(3) 引張弾性率
JIS Ｋ 7113（クロスヘツド速度0.5cm／分）
(4) セン断接着強度
JIS Ｋ 6850
(5) ネジ切り試験
日本水道協会規格JWW AK 132−1982（水
道用ポリエチレン粉体ライニグ鋼管）に記載の
SGP−PCのパイプマシンを使用してのネジ切
り方法で、雰囲気温度を変えて測定し、ネジ切
り可能な最高温度を測定した。
(6) パイプレンチ締め付けトルク試験
日本水道鋼管協会規格WS−033−84（水道用
ポリエチレン粉体ライニング鋼管・外面一層ポ
リエチレン被覆）に記載の万力、パイプレンチ
を使用し、万力で固定した被覆鋼管をパイプレ
ンチで締め、トルクをかけ、樹脂層が変形する
時のトルクを測定した。雰囲気温度は50℃とし
た。
実施例１〜９、比較例１〜４
MIの異なる各LLDPE（コモノマー：ブテン−
１）100部に無水マレイン酸0.6部及び２，５−ジ
メチル−２，５−ジ−（ターシヤリ−ブチルペル
オキシ）−ヘキサン−３ 0.025部を配合し、ヘン
シエルミキサーで混合し、この混合物を６mmφ一
軸押出機に供給し設定温度230℃スクリユー回転
数60rpmで溶融混練して無水マレイン酸変性
LLDPEを得た。この変性LLDPEとポリイソブチ
レン〔エツツ化学社製、ビスタネツクスMML−
80（商品名）未変性LLDPE及びHDPEとを表−１
に示す割合で配合し230℃に加熱溶融混練して組
成物を得た。
得られた各組成物の物性及び各組成物を用いて
各予熱温度の鋼板との積層物を作成して剥離強度
及びセン断接着強度を測定し、その結果を表−１
に示した。
比較のために、MI5ｇ／10分のLLDPEを用い
た場合及びポリイソブチレンに代りエチレンブテ
ンゴム〔三井石油化学社製、Ａ−4085（商品名）、
以下EBRという〕を用いた場合及びHDPEを配
合しない場合についても実施例１と同様にして組
成物の調製及び積層物を作成して物性及び剥離強
度を測定し、その結果を表−１に併記した。
INDUSTRIAL APPLICATION FIELD OF THE INVENTION The present invention relates to modified polyethylene compositions. Conventional technology In the past, polyethylene was coated on the inner and outer surfaces of metal pipes, metal plates, electric wire cables, steel wires, etc. to improve the corrosion resistance, appearance, and food hygiene of metals, or to overcome the drawbacks of various synthetic resins. In order to improve this, composites made by laminating polyethylene are known. In this case, the polyethylene is a composition of modified polyethylene, which is obtained by modifying polyethylene with an unsaturated carboxylic acid or a derivative thereof to give adhesive properties, and synthetic rubber in order to improve its adhesion to metals and various synthetic resins. Are known. For example, a composition consisting of a hydrocarbon synthetic rubber and a modified ethylene polymer that is substantially a medium-low pressure ethylene polymer having a specific melt index ratio grafted with an unsaturated carboxylic acid or a derivative thereof No. 120750), polyethylene modified with an unsaturated carboxylic acid or its anhydride added with a specific ethylene/α-olefin random copolymer is heat-bonded to a metal body coated with an epoxy resin adhesive and heat-treated. How to
168628), a laminate laminated with metal foil through a sheet made of modified polyethylene and polyisobutylene (Japanese Unexamined Patent Publication No. 1983-93541), modified high-density polyethylene, copolymer of ethylene and α-olefin A multilayer laminate structure of a polyamide and a polyethylene composition combined with a rubber-like polymer as required (Japanese Patent Application Laid-open No. 121058/1983) has been proposed. On the other hand, in order to improve the adhesion between metals and thermoplastic resins and polyethylene and their durability, compositions of polyethylene and synthetic rubber, in which specific linear low-density polyethylene is modified with unsaturated carboxylic acids or derivatives thereof ( Japanese Patent Publication No. 57-165413
(Japanese Patent Application Laid-Open No. 2003-120012) and a composition obtained by reacting a mixture of a specific linear low-density polyethylene and synthetic rubber with an unsaturated carboxylic acid or a derivative thereof (Japanese Patent Application Laid-open No.
57-165469) has also been proposed. Problems to be Solved by the Invention Although the adhesive strength between polyethylene and adherends such as metals and thermoplastic resins has been improved in the composition and method proposed above, the adhesion at low preheating temperatures of the adherends has been improved. There wasn't enough about sex. That is, the modified polyethylene or its composition will not exhibit sufficient adhesion unless it is applied to an adherend at a temperature equal to or higher than the melting point of the resin. Therefore, the adherend is usually preheated to a temperature close to the melting temperature of the resin, and its surface is coated with the molten resin. However, when coating a metal object multiple times, for example when coating the inner and outer surfaces of a steel pipe, preheating the steel pipe whose inner surface has been coated first to near the melting point of the resin will soften the already coated surface. Because of the risk of damage and peeling, a resin was needed that could be bonded even if the preheating temperature of the steel pipe was lowered. Furthermore, if the preheating temperature of the adherend cannot be lowered, the cooling rate after coating is slowed down to coat the adherend, resulting in a problem of reduced line speed (production speed). As having sufficient adhesion even when the preheating temperature of the adherend is lower than before,
The present inventors previously proposed a modified polyethylene composition (Japanese Patent Application No. 60-99621) consisting of linear low-density polyethylene having a specific melt index, a modified product, and polyisobutylene. However, although this composition has sufficient adhesion even when the preheating temperature is lowered, the mechanical strength after cooling, such as threading of pipe ends or There remained room for improvement in the practical strength against the torque applied by tightening with a pipe wrench during piping. The present invention solves the above-mentioned problems, has excellent adhesion even when the preheating temperature of the adherend is lowered compared to conventional products, and has high practical mechanical strength. An object of the present invention is to provide an adhesive polyethylene composition having the following properties. Means for Solving the Problems As a result of intensive studies to solve the above problems, the present inventors found that a linear low density polyethylene modified product with a melt index (hereinafter referred to as MI) in a specific range, The present invention was completed by discovering that a composition comprising polyisobutylene and/or a modified product thereof and high-density polyethylene achieves the object of the present invention. That is, the present invention is a modified polyethylene obtained by reacting (A) linear low-density polyethylene with an MI of 7 to 50 g/10 min with an unsaturated carboxylic acid or a derivative thereof.
10-90% by weight, (B) unmodified polyethylene (excluding high-density polyethylene) 0-85% by weight,
(C) 5 to 50% by weight of high-density polyethylene and/or modified high-density polyethylene obtained by reacting the high-density polyethylene with an unsaturated carboxylic acid or its derivative; and (D) polyisobutylene and/or the polyisobutylene is unsaturated. Modified polyisobutylene 5 to 50 obtained by reacting carboxylic acid or its derivative
The gist is an adhesive polyethylene composition consisting of % by weight. The linear low density polyethylene (hereinafter referred to as LLDPE) used in the present invention has an MI of 7 to 50 g/10 min.
In the presence of a chromium-based or Ziegler-based catalyst,
Ethylene and α-olefins, such as butene-1, pentene-
1, hexane-1, 4-methylpentene-1, heptene-1, octene-1, etc., and is produced by copolymerization with MI of 7 to 50.
g/10 minutes, preferably 8 to 20 g/10 minutes. The α-olefin is generally contained in an amount of 3 to 20% by weight. Among these LLDPEs,
Density polymerized by low pressure gas phase method is 0.905 to 0.950g/
cm 3 , weight average molecular weight w/number average molecular weight n is 3
~12 is preferred. MI of above LLDPE is 7
If it is less than 50 g/10 minutes, the adhesion at a low preheating temperature of the adherend will be insufficient, while if it exceeds 50 g/10 minutes, the strength of the resin will be insufficient. Also, MI7~
For polyethylene other than 50g/10min LLDPE,
Adhesion to the adherend and its durability are insufficient. The unmodified polyethylene (excluding high-density polyethylene) used in the present invention is an ethylene homopolymer or copolymer, preferably with a density of 0.910 to
Examples include those with an MI of 0.940 g/cm 3 and an MI of 0.1 to 50 g/10 min. For example, linear low-density polyethylene (hereinafter referred to as
LLDPE), low density polyethylene (hereinafter referred to as
LDPE), medium density polyethylene (hereinafter referred to as
MDPE) or with an ethylene content of 50% by weight
The above examples include copolymers of ethylene and α-olefin or vinyl monomers. High-density polyethylene used in the present invention (hereinafter referred to as
As is well known, HDPE is a polyethylene with a density of 0.941 to 0.970 g/cm 3 obtained by polymerization using a medium-low pressure method, and an MI of 0.1 to 50 g/10 minutes, preferably 1 to 20
g/10 minutes. By blending a specific amount of HDPE, mechanical strength can be improved without reducing adhesiveness. Commercially available polyisobutylene can be used as the polyisobutylene used in the present invention, but Mooney viscosity (Ml 1+4 , 100
℃, JIS K-6300 and below) is 10 to 150, and crystallinity (X-ray diffraction method) is preferably 30% or less. Furthermore, synthetic rubbers other than polyisobutylene do not have sufficient adhesion to adherends. Examples of unsaturated carboxylic acids used in the present invention include acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, citraconic acid, endo-bicyclo[2,2,1]-1,4,5, 6,
7,7-hexacyclo-5-heptene-2,3
-dicarboxylic acid, endo-bi-cyclo-[2,2,
1]-5-heptene-2,3-dicarboxylic acid, cis-4-cyclohexane-1,2-dicarboxylic acid, and the like. Further, examples of derivatives of unsaturated carboxylic acids include acid anhydrides and esters, such as maleic anhydride, citraconic anhydride, endo-bi-cyclo-[2,2,1]-1,4,5,6 ,7,
7-hexachloro-5-heptene-2,3 dicarboxylic anhydride, endo-bicyclo-[2,2,1]
-5-heptene-2,3-dicarboxylic anhydride, cis-4-cyclohexene-1,2-dicarboxylic anhydride, methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, butyl acrylate, butyl methacrylate , maleic acid esters (monoesters, diesters), and the like. Various known methods can be used to react LLDPE, HDPE, or polyisobutylene with an unsaturated carboxylic acid or a derivative thereof. for example,
LLDPE, HDPE, or polyisobutylene and an unsaturated carboxylic acid or its derivative are combined with an organic peroxide initiator, such as di-tertiary-butyl peroxide, dicumyl peroxide, benzoyl, in the presence or absence of a solvent. - oxide,
2,5-dimethyl-2,5-di-(tertiary)
butylperoxy)-hexane-3,2,5-dimethyl-2,5-di-(tertiary-butylperoxy)-hexane, etc. are added, and the mixture is mixed in advance with a mixer such as a Henschel mixer or a ribbon blender. are melt-kneaded using a Banbury mixer, single-screw or multi-screw extruder at a temperature above the melting point of polyethylene or polyisobutylene and below 280°C.
Alternatively, LLDPE, HDPE, or polyisobutylene may be dissolved in a solvent, and an unsaturated carboxylic acid or a derivative thereof and a reaction initiator may be added to the solution to cause the reaction. Here, the amount of unsaturated carboxylic acid or its derivative added to LLDPE, HDPE or polyisobutylene is preferably 0.01 to 3% by weight. Therefore, the amount of the unsaturated carboxylic acid or its derivative and the organic peroxide reaction initiator added is 0.05 to 5 parts by weight of the unsaturated carboxylic acid or its derivative per 100 parts by weight of unmodified LLDPE, HDPE or polyisobutylene. part, reaction initiator 0.001 to 0.5 weight is preferred. In addition, the content of unsaturated carboxylic acid or its derivative in the modified polyethylene or modified polyisobutylene obtained is 0.01
If it is less than 3% by weight, the strong adhesive strength of the present invention cannot be obtained, while if it exceeds 3% by weight, no increase in adhesive strength is observed, and the generation of gel-like substances and discoloration increase, which is also economically disadvantageous. It is. Next, the adhesive polyethylene composition of the present invention is
Modified polyethylene 10~90% by weight, preferably 20~
50% by weight, unmodified polyethylene (excluding HDPE) 0-85% by weight, preferably 0-70% by weight,
It consists of 5-50% by weight, preferably 5-40% by weight of HDPE and/or modified HDPE, and 5-50% by weight, preferably 5-40% by weight of polyisobutylene and/or modified polyisobutylene. If the content of modified polyethylene, unmodified polyethylene, polyisobutylene and/or modified polyisobutylene is outside the above range, adhesion to adherends with low preheating temperatures will be insufficient. Furthermore, if the HDPE content is less than 5% by weight, the mechanical strength is insufficient.
On the other hand, if it exceeds 50% by weight, the adhesion to adherends with low preheating temperatures will be insufficient and the object of the present invention cannot be achieved. The composition of the present invention is prepared by combining modified LLDPE and polyisobutylene and/or modified polyisobutylene.
Furthermore, it can be obtained by mixing these and unmodified polyethylene at the above-mentioned mixing ratio. In order to uniformly disperse each of the above ingredients to create a composition with palatable properties, for example, use a Henschel mixer in advance,
A preferred method is to perform preliminary mixing using a rib blender, etc., and then melt-knead this mixture using a Banbury mixer, roll, extruder, etc. at a temperature from above the melting point of the composition to 280° C. or below. In addition, when polyisobutylene is in the form of a veil, it is desirable to heat and melt-knead it using a Banbury mixer, rolls, or the like. Further, the composition of the present invention may be one in which an unsaturated carboxylic acid or a derivative thereof is reacted with a mixture of LLDPE, HDPE, and polyisobutylene in the above-mentioned mixing ratio. Furthermore, unmodified polyethylene, HDPE and/or
Alternatively, unmodified polyisobutylene may be mixed in the above blending ratio. The composition of the present invention may contain various additives, such as heat stabilizers, ultraviolet absorbers, nucleating agents, antistatic agents, colorants, etc., and various fillers, such as inorganic fillers, plasticizers, etc. I can do it. These additives, etc.
They may be mixed during or after preparation of the composition. The modified polyethylene compositions of the present invention can then form suitable laminates with metals or thermoplastics. Metals in the laminate using the modified polyethylene composition of the present invention include iron, aluminum,
Copper, zinc, nickel, tin, stainless steel, brass, tin, galvanized iron, etc. in plate, foil, cylindrical, tubular,
Examples include lines or other shapes. In addition, as thermoplastic resins, nylon 6, nylon 66, nylon 11, nylon 12, nylon 6
Polyamides such as -10, polyolefins such as olefin homopolymers such as polyethylene, polypropylene, and polybutene or their copolymers, resins that are partially acetalized polyvinyl alcohol (vinylon), and ethylene-vinyl acetate copolymers. Examples include partially hydrolyzed resin (EVAL), polyesters such as polyethylene terephthalate and polybutylene terephthalate, and polyvinyl chloride, with nylon and vinylon being particularly preferred. A laminate using the modified polyethylene composition of the present invention can be obtained by laminating the modified polyethylene composition of the present invention, the above material, and a material selected from metals or thermoplastic resins. The method of obtaining the laminate is not particularly limited, and examples include a method of forming each into a film or sheet and then thermocompression bonding, a method of laminating outside the die, a method of laminating (coextrusion) inside the die, a tube shape or a sheet. Known methods such as extrusion coating or powder coating can be used. In addition, when laminating with metal, pretreatments such as solvent degreasing, pickling, shot blasting, zinc phosphate treatment, calcium phosphate, etc. are usually performed, and further, by using an epoxy resin primer as a primer treatment,
A laminate with stronger adhesive strength can be obtained. As the epoxy resin primer, a one-component or two-component modified epoxy resin primer is preferred from the viewpoint of heat resistance or stability. The structure of the laminate using the modified polyethylene composition of the present invention is basically a two-layer structure in which the modified polyethylene composition of the present invention is laminated with a material selected from the above metals or thermoplastic resins, but as necessary. Various combinations can be made. For example, a modified polyethylene composition (hereinafter referred to as the composition)/
Metal, the composition/thermoplastic resin, the composition/metal/the composition, metal/the composition/metal, metal/the composition/thermoplastic resin, thermoplastic resin/the composition/thermoplastic resin, etc. It is also possible to combine these and other materials such as fibers, paper, wood boards, etc. The composition of the present invention forms a suitable composite (coating, lamination, etc.) with metal or thermoplastic resin as described above, and is particularly useful for coating metal pipes.
An example of manufacturing a resin-coated metal tube will be described below. The base metal tube is cleaned by surface treatment such as shotplast, gridplast, or pickling. Furthermore, it is desirable to apply an epoxy adhesive or the like on this as a primer treatment in order to obtain a resin layer with stronger adhesive strength. The pretreated metal tube is heated to a desired temperature, such as 100°C or higher, preferably 110 to 150°C, by high-frequency induction heating or the like.
The outer surface of the metal tube is coated with the composition by extruding it into a tube shape or wrapping it into a sheet shape at a temperature above the melting point, preferably from 200 to 230°C. The thickness of the coating varies depending on the purpose, but is usually around 0.3 mm. Further, an exterior material such as polyolefin, preferably high-density polyethylene, is extruded onto the tube at a temperature above the melting point, preferably from 200 to 230 DEG C., or wrapped in a sheet, and immediately cooled with water. The thickness of the exterior material is usually about 2 mm. Note that the covering of the exterior material may be omitted as appropriate depending on the application. In addition, if the above metal pipe coating is applied to both the inside and outside of the metal pipe, the pretreated metal pipe should be coated with 100%
It is heated to ~150°C, and the inner surface is powder coated with the composition and polyolefin, preferably polyethylene, in this order to form a resin layer. Next, this inner-coated metal tube is heated to a temperature of 100° C. to less than the melting point of the inner-coated resin, and the outer surface of this metal tube is coated with the composition and polyolefin in the same manner as described above. Effects of the Invention The composition of the present invention is superior to modified polyethylene compositions that have already been proposed, from lower preheating temperatures to higher temperatures for adherends such as metals and thermoplastic resins. It shows the adhesion strength. Therefore, in multilayer resin coating, there is no inconvenience caused by softening or melting of the already coated layer, and there is no need to slow down the cooling rate after coating, so there is no reduction in production rate. In addition, the composition of the present invention has improved mechanical strength after adhesion compared to conventional compositions, so it has sufficient strength for practical use, such as thread cutting resistance and pipe wrench torque resistance in coated steel pipes, for example. . Due to the excellent properties described above, the composition of the present invention is suitable for composites with metals and thermoplastic resins, particularly for multilayer composites. As an example of compounding,
The inner and outer surfaces of steel pipes and cast iron pipes, coatings of steel plates, metal foils, electric wire cables, steel wires, etc., or tank linings, or multilayer films of various thermoplastic resins,
Examples include laminates such as sheets, bottles, containers, etc. Examples Next, the present invention will be explained in detail by giving examples. In addition, all parts and percentages in the examples are based on weight, and the test method is as follows. (1) MI ASTM D-1238E (190℃, 2160g) (2) Peel strength After electrolytically degreasing a pickled steel plate (SS-41) 100 x 100 x 0.3 mm, preheat it to the specified temperature on a heating plate, On top of this, a sheet of the composition of the present invention (thickness 1
A test piece was prepared by heating a sheet of high-density polyethylene (3 mm thick) to 220° C., melting and bonding the sheet, allowing it to stand for 10 seconds, then cooling it by immersing it in running water. The resin layer of the test piece was cut to a width of 10 mm, a portion was peeled off as a gripping margin, and the 90° peel strength was measured at 23 mm at a peel rate of 50 mm/min using an Instron tensile tester.
℃ and 50℃. (3) Tensile modulus JIS K 7113 (Crosshead speed 0.5cm/min) (4) Shear adhesive strength JIS K 6850 (5) Thread cutting test Japan Water Works Association standard JWW AK 132-1982 (Polyethylene powder lined steel pipe for water supply ) stated in
Using a thread cutting method using an SGP-PC pipe machine, measurements were taken while varying the ambient temperature, and the maximum temperature at which thread cutting was possible was measured. (6) Pipe wrench tightening torque test Use a vise and pipe wrench as described in the Japan Water Works Steel Pipe Association standard WS-033-84 (polyethylene powder-lined steel pipes for water supply, single-layer polyethylene coating on the outside), and use a pipe wrench to fix the coating in a vise. The steel pipe was tightened with a pipe wrench, torque was applied, and the torque at which the resin layer deformed was measured. The ambient temperature was 50°C. Examples 1 to 9, Comparative Examples 1 to 4 Each LLDPE with different MI (comonomer: butene-
1) Blend 0.6 parts of maleic anhydride and 0.025 parts of 2,5-dimethyl-2,5-di-(tertiary-butylperoxy)-hexane-3 to 100 parts, mix with a Henschel mixer, and mix this mixture into a 6 mmφ Supply to a single screw extruder and melt-knead at a set temperature of 230℃ and screw rotation speed of 60rpm to modify with maleic anhydride.
Got LLDPE. This modified LLDPE and polyisobutylene [manufactured by Etsu Kagaku Co., Ltd., Vistanecs MML-
80 (product name) unmodified LLDPE and HDPE Table-1
A composition was obtained by blending the ingredients in the proportions shown below and heating, melting and kneading them at 230°C. Using the physical properties of each composition obtained and each composition, a laminate with a steel plate of each preheating temperature was prepared and the peel strength and shear adhesive strength were measured, and the results are shown in Table 1.
It was shown to. For comparison, when LLDPE with MI of 5 g/10 min was used and ethylene butene rubber [manufactured by Mitsui Petrochemical Co., Ltd., A-4085 (trade name)] was used instead of polyisobutylene.
In the case of using EBR (hereinafter referred to as EBR) and the case of not incorporating HDPE, compositions were prepared and laminates were prepared in the same manner as in Example 1, and the physical properties and peel strength were measured, and the results are also listed in Table 1. did.
【表】【table】
【表】
実施例10、比較例５
供試金属管として50mmφSGP黒管を酸洗処理に
より脱スケールした後、高周波誘導加熱により表
−２に示す各温度に加熱し、この鋼管に実施例５
で用いた変性ポリエチレン組成物を65mmφの押出
機にて樹脂温度220℃で、厚さ１mm、ライン速度
１ｍ／分でチユーブ状に押出被覆し、ダイスとの
距離３cmの水槽で冷却して樹脂被覆鋼管を得た。
得られた被覆鋼管の剥離強度及び物性を表−２に
示した。
比較のために、比較例４の組成物を用いた以外
は実施例10と同様にして樹脂被覆鋼管を得た。得
られた被覆鋼管の剥離強度及び物性を表−２に併
記した。[Table] Example 10, Comparative Example 5 A 50 mmφ SGP black tube was descaled by pickling treatment as a test metal tube, and then heated to each temperature shown in Table 2 by high frequency induction heating.
The modified polyethylene composition used in was extruded into a tube shape at a resin temperature of 220°C with a thickness of 1 mm and a line speed of 1 m/min using a 65 mmφ extruder, and was cooled in a water tank with a distance of 3 cm from the die to form a resin coating. Obtained steel pipe.
The peel strength and physical properties of the obtained coated steel pipe are shown in Table 2. For comparison, a resin-coated steel pipe was obtained in the same manner as in Example 10, except that the composition of Comparative Example 4 was used. The peel strength and physical properties of the obtained coated steel pipe are also listed in Table 2.
【表】【table】
【表】
実施例 11、12
実施例１と４で用いた未変性LLDPE、HDPE
及びポリイソブチレンを表−３に示す割合で混合
した後、この混合物に無水マレイン酸と実施例１
と同様の方法で反応させて変性ポリエチレン組成
物を得た。得られた該組成物を用いて鋼板との積
層物を作成し、物性及び剥離強度を測定してその
結果を表−３に示した。[Table] Examples 11 and 12 Unmodified LLDPE and HDPE used in Examples 1 and 4
and polyisobutylene in the proportions shown in Table 3, maleic anhydride and Example 1 were added to this mixture.
A modified polyethylene composition was obtained by reacting in the same manner as above. A laminate with a steel plate was prepared using the obtained composition, and the physical properties and peel strength were measured and the results are shown in Table 3.
【表】【table】
Claims (1)
低密度ポリエチレンに、不飽和カルボン酸もしく
はその誘導体を反応させてなる変性ポリエチレン
10〜90重量％、(B)未変性ポリエチレン（但し、高
密度ポリエチレンを除く）０〜85重量％、(C)高密
度ポリエチレン及び／又は該高密度ポリエチレン
に不飽和カルボン酸もしくはその誘導体を反応さ
せてなる変性高密度ポリエチレン５〜50重量％及
び(D)ポリイソブチレン及び／又は該ポリイソブチ
レンに不飽和カルボン酸もしくはその誘導体を反
応させてなる変性ポリイソブチレン５〜50重量％
とからなる接着性ポリエチレン組成物。1 (A) Modified polyethylene obtained by reacting linear low-density polyethylene with a melt index of 7 to 50 g/10 min with an unsaturated carboxylic acid or a derivative thereof.
10-90% by weight, (B) unmodified polyethylene (excluding high-density polyethylene) 0-85% by weight, (C) high-density polyethylene and/or reacting the high-density polyethylene with an unsaturated carboxylic acid or its derivative and (D) polyisobutylene and/or 5 to 50% by weight of modified polyisobutylene obtained by reacting the polyisobutylene with an unsaturated carboxylic acid or a derivative thereof.
An adhesive polyethylene composition consisting of.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25767585A JPS62119248A (en) | 1985-11-19 | 1985-11-19 | Adhesive polyethylene composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25767585A JPS62119248A (en) | 1985-11-19 | 1985-11-19 | Adhesive polyethylene composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62119248A JPS62119248A (en) | 1987-05-30 |
| JPH0528265B2 true JPH0528265B2 (en) | 1993-04-23 |
Family
ID=17309539
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP25767585A Granted JPS62119248A (en) | 1985-11-19 | 1985-11-19 | Adhesive polyethylene composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62119248A (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2855439B2 (en) * | 1989-03-28 | 1999-02-10 | 三菱化学株式会社 | Method for producing composite sheet for hot melt bonding |
| JPH03277501A (en) * | 1990-03-09 | 1991-12-09 | Tatsuta Electric Wire & Cable Co Ltd | Plywood |
| JPH03278901A (en) * | 1990-03-28 | 1991-12-10 | Tatsuta Electric Wire & Cable Co Ltd | Adhesive sheet for plywood |
| JP2614352B2 (en) * | 1990-08-10 | 1997-05-28 | 昭和電工株式会社 | Polyethylene resin composition |
| US5643997A (en) * | 1990-08-10 | 1997-07-01 | Showa Denko K.K. | Polyethylenic resin composition |
| JPH04113805A (en) * | 1990-09-04 | 1992-04-15 | Tatsuta Electric Wire & Cable Co Ltd | Plywood |
| JPH04113801A (en) * | 1990-09-04 | 1992-04-15 | Tatsuta Electric Wire & Cable Co Ltd | Plywood |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56120750A (en) * | 1980-02-29 | 1981-09-22 | Mitsui Petrochem Ind Ltd | Modified ethylene polymer composition |
| JPS57165413A (en) * | 1981-04-07 | 1982-10-12 | Toa Nenryo Kogyo Kk | Modified polyethylene and its laminate |
| JPS57170940A (en) * | 1981-04-15 | 1982-10-21 | Idemitsu Kosan Co Ltd | Polyolefin resin composition and its laminate |
| JPS59179543A (en) * | 1983-03-30 | 1984-10-12 | Mitsubishi Chem Ind Ltd | Adhesive polyethylene composition |
-
1985
- 1985-11-19 JP JP25767585A patent/JPS62119248A/en active Granted
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56120750A (en) * | 1980-02-29 | 1981-09-22 | Mitsui Petrochem Ind Ltd | Modified ethylene polymer composition |
| JPS57165413A (en) * | 1981-04-07 | 1982-10-12 | Toa Nenryo Kogyo Kk | Modified polyethylene and its laminate |
| JPS57170940A (en) * | 1981-04-15 | 1982-10-21 | Idemitsu Kosan Co Ltd | Polyolefin resin composition and its laminate |
| JPS59179543A (en) * | 1983-03-30 | 1984-10-12 | Mitsubishi Chem Ind Ltd | Adhesive polyethylene composition |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62119248A (en) | 1987-05-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4198327A (en) | Grafted polyolefin composition having improved adhesiveness | |
| US4440911A (en) | Modified polyethylene and laminate thereof | |
| JP5226309B2 (en) | Adhesive compositions derived from highly functionalized ethylene copolymers | |
| JP2917546B2 (en) | Adhesive resin composition | |
| US4460646A (en) | Adhesive resin composition and laminate thereof | |
| JPS6325006B2 (en) | ||
| JPH0551496A (en) | Adhesive or coating composition and use thereof | |
| JPH0528265B2 (en) | ||
| JPS6011056B2 (en) | Modified ethylene polymer composition | |
| JP6583997B2 (en) | Adhesive manufacturing method, adhesive, adhesive laminate, and laminate | |
| JPH0528266B2 (en) | ||
| JPS5936586B2 (en) | Multilayer laminated structure | |
| JPH0528263B2 (en) | ||
| JP2761547B2 (en) | Adhesive resin composition and coated steel pipe using the same | |
| JPH0528264B2 (en) | ||
| JPH0530858B2 (en) | ||
| JPS629423B2 (en) | ||
| JP2019196496A (en) | Adhesive resin composition, and adhesive | |
| JPH0625293B2 (en) | Modified polyethylene composition | |
| JPH0649814B2 (en) | Modified olefin polymer composition | |
| JP3613992B2 (en) | Resin composition for extrusion lamination and laminate using the same | |
| JPH0794508B2 (en) | Method for producing modified olefin polymer | |
| JPH0149402B2 (en) | ||
| JPS6210187B2 (en) | ||
| JPH06107873A (en) | Adhesive resin composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |