JPS62220524A - Heat-resistant shrinkable film - Google Patents
Heat-resistant shrinkable filmInfo
- Publication number
- JPS62220524A JPS62220524A JP61064597A JP6459786A JPS62220524A JP S62220524 A JPS62220524 A JP S62220524A JP 61064597 A JP61064597 A JP 61064597A JP 6459786 A JP6459786 A JP 6459786A JP S62220524 A JPS62220524 A JP S62220524A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- film
- composition
- silane
- group
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 claims abstract description 21
- -1 polyethylene Polymers 0.000 claims abstract description 18
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 12
- 229920001400 block copolymer Polymers 0.000 claims abstract description 10
- 150000001993 dienes Chemical class 0.000 claims abstract description 8
- 229920005989 resin Polymers 0.000 claims abstract description 7
- 239000011347 resin Substances 0.000 claims abstract description 7
- 239000003054 catalyst Substances 0.000 claims abstract description 5
- 229920001112 grafted polyolefin Polymers 0.000 claims abstract description 5
- 229910000077 silane Inorganic materials 0.000 claims abstract description 5
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000000962 organic group Chemical group 0.000 claims abstract description 3
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 claims abstract 2
- 229920002857 polybutadiene Polymers 0.000 claims description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 229920005672 polyolefin resin Polymers 0.000 claims description 4
- 229920006302 stretch film Polymers 0.000 claims description 4
- 239000005062 Polybutadiene Substances 0.000 claims description 2
- 150000002430 hydrocarbons Chemical group 0.000 claims description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 1
- 229920005992 thermoplastic resin Polymers 0.000 abstract description 6
- 239000004698 Polyethylene Substances 0.000 abstract description 2
- 238000009833 condensation Methods 0.000 abstract description 2
- 230000005494 condensation Effects 0.000 abstract description 2
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 abstract description 2
- 238000001125 extrusion Methods 0.000 abstract description 2
- 229920000573 polyethylene Polymers 0.000 abstract description 2
- 238000013329 compounding Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000004132 cross linking Methods 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 abstract 1
- 238000000034 method Methods 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 210000000689 upper leg Anatomy 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- MASNVFNHVJIXLL-UHFFFAOYSA-N ethenyl(ethoxy)silicon Chemical compound CCO[Si]C=C MASNVFNHVJIXLL-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920006132 styrene block copolymer Polymers 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
Landscapes
- Absorbent Articles And Supports Therefor (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesive Tapes (AREA)
Abstract
Description
【発明の詳細な説明】
(発明の技術分野)
本発明は充分な耐熱性を有し、しかも伸縮性に優れた耐
熱性伸縮フィルムに関する。DETAILED DESCRIPTION OF THE INVENTION (Technical Field of the Invention) The present invention relates to a heat-resistant stretchable film that has sufficient heat resistance and excellent stretchability.
(発明の技術的背景及びその問題点)
従来、例えば紙おむつ等の装着時に太股部への密着性を
良くするため、紙おむつと太股部が密着する紙おむつ側
部分にゴム紐、発泡ウレタン、ブタジェンゴムとスチレ
ン−ブタジェン−スチレンブロック共重合体との混合物
(以下、RB/SBSと略す。)などを延伸した状態で
貼り付け、後に張力を取り去り、ゴム紐などの伸張の回
復性を利用し、伸縮性のあるギヤザ一部を設ける方法が
取られていた。しかしながら、ゴム紐および発泡ポリウ
レタンは高価であり、又RB/8BSは発泡ポリウレタ
ンより価格的には相当なメリットがあるが、耐熱性に劣
るため、紙おむつとRB/8B8との張り合せ方法の一
つであるホットメルトで紙おむつに接着する方法におい
ても、フィルムが切れたり穴があいたりして、実用に供
されないという欠点があった。(Technical background of the invention and its problems) Conventionally, in order to improve the adhesion to the thighs when wearing a disposable diaper, for example, rubber cords, urethane foam, butadiene rubber, and styrene have been used on the side of the disposable diaper where the thighs come into close contact with the diaper. - A mixture of butadiene and styrene block copolymer (hereinafter abbreviated as RB/SBS) is pasted in a stretched state, the tension is removed later, and the elasticity is A method was used in which a certain gear was provided. However, rubber cords and foamed polyurethane are expensive, and although RB/8BS has a considerable advantage over foamed polyurethane in terms of price, it is inferior in heat resistance, so one of the methods for bonding disposable diapers and RB/8B8 is The method of adhering paper diapers to paper diapers using hot melt also had the disadvantage that the film would be cut or punctured, making it impractical.
上記欠点は他の張り合せ方法を用いた場合も同様である
。The above drawbacks also apply when other bonding methods are used.
(発明の目的)
本発明はこのような欠点を解消するためになされたもの
で、フィルムと紙おむつを接着する際にフィルムが破断
したりあるいは穴があいたりすることがなく、従って耐
熱性に優れた耐熱性伸縮フィルムを提供するものである
。(Purpose of the Invention) The present invention has been made to eliminate these drawbacks, and the film does not break or become punctured when bonding the film and paper diaper, and therefore has excellent heat resistance. The present invention provides a heat-resistant stretch film.
(発明の概要)
すなわち本発明の耐熱性伸縮フィルムは(4)ブタジェ
ン樹脂および/またはポリオレアイン樹11ii+20
〜80重量%と芳香族ビニル化合物−共役ジエンブロッ
ク共鼠合体80〜20重量%とからなる組成物100瓜
量部に(B)一般式RR/8 i Yx (ただし几は
オレフィン性不飽和の1価の炭化水素基またはハイドロ
カーボンオキシ基であり、Yは加水分解しうる有機基で
あって、R′は基孔または基Yである)で表わされるシ
ラン化合物を反応せしめたシラングラフト化ポリオレフ
ィン樹脂から成る組成物5〜100重量部との混合物か
ら成るフィルムをシラノール触媒の存在下で微量の水分
と作用せしめることを特徴としている。(Summary of the invention) That is, the heat-resistant stretch film of the present invention comprises (4) butadiene resin and/or polyolein resin 11ii+20
80% by weight of the aromatic vinyl compound-conjugated diene block copolymer, and 80% to 20% by weight of the aromatic vinyl compound-conjugated diene block copolymer. A silane-grafted polyolefin reacted with a silane compound represented by a monovalent hydrocarbon group or a hydrocarbonoxy group, Y is a hydrolyzable organic group, and R' is a pore or a group Y. It is characterized in that a film made of a mixture of 5 to 100 parts by weight of a resin composition is allowed to react with a trace amount of moisture in the presence of a silanol catalyst.
ポリオレアイン樹脂としてはポリエチレン、ポリプロピ
レン、ポリブテン、エチレン−酢酸ビニル共重合体(’
JAVA )などがある。これらの樹脂は単独または2
種以上を混合して使用することかで上、特に好ましくは
85%以上で、更にその結晶的は結晶化度が5%未満で
はフィルムとしての強は広い範囲にわたって選択が可能
であるが成形性およびフィルムとしての強度の点からト
ルエン溶液30°Cで測定した固有粘度〔η〕0.5以
上1特に0.7〜1.5のものが好ましい。Polyoleain resins include polyethylene, polypropylene, polybutene, ethylene-vinyl acetate copolymer ('
JAVA) etc. These resins may be used alone or in combination.
The crystallinity is preferably 85% or more, and if the crystallinity is less than 5%, the strength as a film can be selected from a wide range, but the moldability From the viewpoint of strength as a film, it is preferable that the intrinsic viscosity [η] measured in toluene solution at 30° C. is 0.5 or more and 1, particularly 0.7 to 1.5.
本発明に使用する芳香族ビニル化合物−共役ジエンブロ
ック共重合体の芳香族ビニル化合物としては、スチレン
、α−メチルスチレンなどが用いが用いられる。As the aromatic vinyl compound of the aromatic vinyl compound-conjugated diene block copolymer used in the present invention, styrene, α-methylstyrene, etc. are used.
このブロック共重合体は分子量が50,000〜250
.000で芳香族ビニル化合物の含有量が5〜50重景
%のものが好適に使用される。分子量が高すぎると成形
性が悪くなり、低すぎるとフィルムとしての強度が低下
する。芳香族ビニル化合物の含有量が前記の範囲より多
い場合には伸縮性が損われ、少ない場合にはフィルムと
しての強度が低下する。This block copolymer has a molecular weight of 50,000 to 250
.. 000 and the aromatic vinyl compound content is preferably 5 to 50% by weight. If the molecular weight is too high, the moldability will be poor, and if the molecular weight is too low, the strength as a film will be reduced. If the content of the aromatic vinyl compound is more than the above range, the elasticity will be impaired, and if it is less, the strength of the film will be reduced.
ブロック共重合体の構造については、特に制限がなく、
使用可能である。There are no particular restrictions on the structure of the block copolymer;
Available for use.
又(4)の組成物においてブタジェン樹脂および/また
はポリオレフィン樹脂からなる熱可塑性樹脂と芳香族ビ
ニル化合物−共役ジエンブロック共重合体との混合比は
成形性、伸縮性の点から熱可塑性樹脂20〜80重量%
に対し、芳香族ビニル−共役ジエンブロック共重合体8
0〜20重量%、特に好ましくは熱可塑性樹脂30〜7
0重量%に対し、芳香族ビニル化合物−共役ジエンブロ
ック共重合体70〜30重量%である。その理由は熱可
塑性樹脂が20重量外未満では成形性が悪くなり、80
重R%を越えると伸縮性が損なわれるためである。In addition, in the composition (4), the mixing ratio of the thermoplastic resin consisting of butadiene resin and/or polyolefin resin and the aromatic vinyl compound-conjugated diene block copolymer is 20 to 20 for the thermoplastic resin from the viewpoint of moldability and stretchability. 80% by weight
On the other hand, aromatic vinyl-conjugated diene block copolymer 8
0-20% by weight, particularly preferably thermoplastic resin 30-7%
0% by weight, the aromatic vinyl compound-conjugated diene block copolymer is 70 to 30% by weight. The reason for this is that if the weight of the thermoplastic resin is less than 20%, the moldability will be poor;
This is because if the weight R% is exceeded, elasticity will be impaired.
又、■の組成物はEVA、エチレン・アクリル酢エチル
共重合体(li:1fA)、エチレン・アクリル酢共重
合体(BAム)あるいはエチレンプロピレン共重合体(
EPR)等のグラフト化可能なポリオレフィン樹脂に例
えば0.01〜5.0重it%のビニルトリメトキシシ
ラン(V’I’MO8)、ビニルエトキシシランの如き
シラン化合物をグラフト化せしめることにより得られる
。In addition, the composition (2) contains EVA, ethylene/acrylic ethyl acetate copolymer (li:1fA), ethylene/acrylic vinegar copolymer (BAM), or ethylene propylene copolymer (
It is obtained by grafting a silane compound such as vinyltrimethoxysilane (V'I'MO8) or vinylethoxysilane in an amount of 0.01 to 5.0 wt % to a graftable polyolefin resin such as EPR). .
t−コでAVA、EEA、EAAc7)VA (BA、
AA)含有量としては10重量%未満の場合は充分な接
着性、柔軟性が得られず、50重ffi%を越えると充
分な耐摩耗性、機械的強度が得られないので10〜50
重量%の範囲での使用が好ましい。AVA, EEA, EAAc7) VA (BA,
AA) If the content is less than 10% by weight, sufficient adhesion and flexibility cannot be obtained, and if it exceeds 50% by weight, sufficient abrasion resistance and mechanical strength cannot be obtained.
It is preferred to use a range of % by weight.
又、FiPRのPP含有量としては20重量%未満ある
いは80重量%を越えると充分な弾性が得られないので
20〜80重量%の範囲での使用が好ましい。Further, if the PP content of FiPR is less than 20% by weight or more than 80% by weight, sufficient elasticity cannot be obtained, so it is preferably used in the range of 20 to 80% by weight.
次いで(2)の組成物と(至)の組成物から成るフィル
ムを例えばジブチルチンジラウレート、ジブチルチンジ
アセテートの如きシラノール縮合触g o、oos〜1
0重景%の存在下において大気中に放置することにより
架橋させる。Next, a film consisting of the composition (2) and the composition (to) is treated with a silanol condensation catalyst such as dibutyltin dilaurate or dibutyltin diacetate.
It is crosslinked by leaving it in the atmosphere in the presence of 0 weight percent.
本発明において(4)の組成物と(B)の組成物との混
合比は耐熱性、伸縮性の点から(4)の組成物100重
量部に対しく至)の組成物5〜100重量部とする。In the present invention, the mixing ratio of the composition (4) and the composition (B) is from 5 to 100 parts by weight of the composition (4) to 100 parts by weight of the composition (4) from the viewpoint of heat resistance and elasticity. Department.
その理由は(Bの組成物が5重量部未満では充分な耐熱
性が得られず、100重i部を越えると伸縮性が不足す
るためである。The reason for this is that if the composition of B is less than 5 parts by weight, sufficient heat resistance cannot be obtained, and if it exceeds 100 parts by weight, elasticity is insufficient.
本発明組成物の混合方法は一般に用いられる混合方法が
用いられ、又伸縮フィルムの製造方法としては、インフ
レーション成形、Tダイ成形など通常の溶融押出成形法
が好適に用いられる。A commonly used mixing method can be used to mix the composition of the present invention, and a conventional melt extrusion molding method such as inflation molding or T-die molding is preferably used as a method for producing a stretch film.
(実施例) 以下実施例について説明する。(Example) Examples will be described below.
実施例1〜3、比較例
表に示した(4)の組成物にGP、!=CMの比を9=
1にした(B)の組成物を混合し、スクリュー押出機に
より50μ票の厚さのフィルムに成形した。次いで、こ
のフィルムを固定治具により固定し所定温度にシリコー
ンオイル浴にて加熱した2鴎φの熱球をフィルムの中心
部に落下させ、破断した時の温度を測定した。又、50
%延伸時のフィルム破断温度も併せて測定し、前記の試
験を行った結果を同表に示した。GP to the composition (4) shown in Examples 1 to 3 and Comparative Example Table. =CM ratio is 9=
The composition (B) prepared in Example 1 was mixed and formed into a film having a thickness of 50 μm using a screw extruder. Next, this film was fixed with a fixing jig, and a 2 mm diameter hot bulb heated to a predetermined temperature in a silicone oil bath was dropped onto the center of the film, and the temperature at which it broke was measured. Also, 50
The film breaking temperature at the time of % stretching was also measured, and the results of the above tests are shown in the same table.
以 下 余 白
(※1) −!1−B820(日本合成ゴム社の商品
名)
(※2) カリフレックス(アロン化成社の商品名)
(※3) NUO−3195(日本ユニカー社の商品
名iVAコンテント25重量
%)
(発明の効果)
以上述べたように本発明においてはブタジェン樹脂およ
び/またはポリオレフィン樹脂と芳香族ビニル化合物に
シラングラフト化ポリオレフィン樹脂を混合し架橋しで
あるので、得られたフィルムは充分な伸縮性を有ししか
も耐熱性に優れている0Below margin (*1) -! 1-B820 (trade name of Nippon Gosei Rubber Co., Ltd.) (*2) Califlex (trade name of Aron Kasei Co., Ltd.) (*3) NUO-3195 (trade name of Nippon Unicar Co., Ltd. iVA content 25% by weight) (Effects of the invention ) As mentioned above, in the present invention, a butadiene resin and/or a polyolefin resin, an aromatic vinyl compound, and a silane-grafted polyolefin resin are mixed and crosslinked, so the obtained film has sufficient elasticity and Excellent heat resistance0
Claims (1)
ン樹脂20〜80重量%と芳香族ビニル化合物−共役ジ
エンブロック共重合体80〜20重量%とからなる組成
物100重量部と(B)一般式RR′SiY_2(ただ
しRはオレフィン性不飽和の1価の炭化水素基またはハ
イドロカーボンオキシ基でありYは加水分解しうる有機
基であつて、R′は基Rまたは基Yである)で表わされ
るシラン化合物を反応せしめたシラングラフト化ポリオ
レフィン樹脂から成る組成物5〜100重量部との混合
物から成るフィルムをシラノール触媒の存在下で微量の
水分と作用せしめることを特徴とする耐熱性伸縮フィル
ム。 2、ブタジエン樹脂が1,2結合含有量70%以上、結
晶化度5〜40%、固有粘度〔η〕(トルエン中30℃
で測定)0.7(dl/g)以上の1,2ポリブタジエ
ンである特許請求の範囲第1項記載の耐熱性伸縮フィル
ム。[Scope of Claims] 1. (A) 100 parts by weight of a composition consisting of 20 to 80% by weight of a butadiene resin and/or polyolefin resin and 80 to 20% by weight of an aromatic vinyl compound-conjugated diene block copolymer; B) General formula RR'SiY_2 (where R is an olefinically unsaturated monovalent hydrocarbon group or a hydrocarbonoxy group, Y is a hydrolyzable organic group, and R' is a group R or a group Y) A heat-resistant film comprising a mixture of 5 to 100 parts by weight of a composition comprising a silane grafted polyolefin resin reacted with a silane compound represented by (1) and a trace amount of moisture in the presence of a silanol catalyst. stretchable film. 2. The butadiene resin has a 1,2 bond content of 70% or more, a crystallinity of 5 to 40%, an intrinsic viscosity [η] (30°C in toluene)
2. The heat-resistant stretch film according to claim 1, which is 1,2 polybutadiene having a polybutadiene of 0.7 (dl/g) or more (measured by dl/g).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61064597A JPS62220524A (en) | 1986-03-21 | 1986-03-21 | Heat-resistant shrinkable film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61064597A JPS62220524A (en) | 1986-03-21 | 1986-03-21 | Heat-resistant shrinkable film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62220524A true JPS62220524A (en) | 1987-09-28 |
Family
ID=13262821
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61064597A Pending JPS62220524A (en) | 1986-03-21 | 1986-03-21 | Heat-resistant shrinkable film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62220524A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1577338A1 (en) * | 2004-02-26 | 2005-09-21 | FAIT PLAST S.p.A. | Method for crosslinking a thermoplastic composition and thermoplastic film thus produced |
CN110234697A (en) * | 2017-01-30 | 2019-09-13 | 信越化学工业株式会社 | The resin combination and installation circuit substrate of room temp solidified silane-containing |
-
1986
- 1986-03-21 JP JP61064597A patent/JPS62220524A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1577338A1 (en) * | 2004-02-26 | 2005-09-21 | FAIT PLAST S.p.A. | Method for crosslinking a thermoplastic composition and thermoplastic film thus produced |
CN110234697A (en) * | 2017-01-30 | 2019-09-13 | 信越化学工业株式会社 | The resin combination and installation circuit substrate of room temp solidified silane-containing |
CN110234697B (en) * | 2017-01-30 | 2022-11-18 | 信越化学工业株式会社 | Room temperature-curable silane-containing resin composition and circuit board mounted with the same |
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