JPS6342837A - Manufacture of oriented film - Google Patents
Manufacture of oriented filmInfo
- Publication number
- JPS6342837A JPS6342837A JP18646586A JP18646586A JPS6342837A JP S6342837 A JPS6342837 A JP S6342837A JP 18646586 A JP18646586 A JP 18646586A JP 18646586 A JP18646586 A JP 18646586A JP S6342837 A JPS6342837 A JP S6342837A
- Authority
- JP
- Japan
- Prior art keywords
- roll
- sheet
- thereafter
- resin
- rolls
- 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
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 11
- 239000004744 fabric Substances 0.000 claims abstract description 6
- 239000011347 resin Substances 0.000 abstract description 29
- 229920005989 resin Polymers 0.000 abstract description 29
- 238000000034 method Methods 0.000 abstract description 14
- 230000008569 process Effects 0.000 abstract description 5
- 229920001971 elastomer Polymers 0.000 abstract description 4
- 239000005060 rubber Substances 0.000 abstract description 4
- 230000007547 defect Effects 0.000 abstract description 3
- 238000004049 embossing Methods 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract description 2
- 238000007731 hot pressing Methods 0.000 abstract 2
- 238000004804 winding Methods 0.000 abstract 1
- 238000000465 moulding Methods 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 5
- 230000002950 deficient Effects 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229940117958 vinyl acetate Drugs 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- QUGNZNCOLVCQKW-UHFFFAOYSA-M S[Sn] Chemical compound S[Sn] QUGNZNCOLVCQKW-UHFFFAOYSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
Landscapes
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は延伸フィルムの9a造方法、とくには穴あき不
良を解消するためのa層シートよりの延伸フィルムの製
造方法に関する。DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention relates to a method for producing a stretched film (9a), and particularly to a method for producing a stretched film from an A-layer sheet to eliminate hole defects.
(従来技術とその問題点)
従来の延伸フィルムの製造方法としては、Tダイ成形法
またはカレンダー成形法により成形された原反(シート
)を、延伸工程に導いて延伸するのが普通であり、延伸
フィルムのそれぞれの用途に応じて延伸倍率200〜5
00%でもって、延伸後のフィルム厚みを10〜70#
Lmとしていた。この延伸フィルムにおける品質上の問
題は表裏に貫通する穴あきの発生(1,000m中に米
粒大3個で不良となる)であり、その原因は原反に混入
された異物が延伸に追従できないことのために起るもの
と考えられている。(Prior art and its problems) As a conventional method for producing a stretched film, it is normal to lead a raw fabric (sheet) formed by a T-die molding method or a calendar molding method to a stretching process and stretch it. The stretching ratio is 200 to 5 depending on the purpose of the stretched film.
00%, the film thickness after stretching is 10~70#
It was set to Lm. The quality problem with this stretched film is the occurrence of holes that penetrate through the front and back sides (3 rice-grain-sized holes in 1,000 m are considered defective), and the cause of this is that foreign matter mixed in the original film cannot follow the stretching. It is thought to occur because of
この異物の混入径路としてはl 原料自体に混入されて
いるか、配合成分例えば顔料、充填剤などが二次的に凝
集して異物となるもの、 2 成形または延伸工程中に
おいて基材樹脂自体が分解または変質して生ずる副生物
、3 ′!II造工程中において系外から混入するも
のなどがあるが、混入した異物を延伸部に取り出して除
去することは不Of能であり、このために穴あきの発生
を防止する改S策の出現が強く求められていた。The paths for this foreign matter to enter are: (1) It is mixed into the raw material itself, or it becomes a foreign matter due to secondary aggregation of blended components such as pigments and fillers, and (2) The base resin itself decomposes during the molding or stretching process. Or by-products resulting from deterioration, 3'! During the II manufacturing process, some foreign matter gets mixed in from outside the system, but it is impossible to remove the mixed foreign matter by taking it out to the stretching section, and for this reason, new S measures have been developed to prevent the occurrence of holes. It was strongly requested.
(問題点を解決するための手段)
本9.IJlは穴あきシートの発生を未然に防止する延
伸フィルムのsII造方決方法するもので、成形された
原反を2層以上積み重ねて合着させた後、延伸すること
を要旨とするものである。(Means for solving problems) Book 9. IJl is a sII manufacturing method for stretched film that prevents the formation of perforated sheets, and its gist is to stack two or more formed raw films, fuse them together, and then stretch them. be.
これを説1j1すると、本発明者は穴あき不良延伸フィ
ル11の原反の厚みと異物の大きさとの関係な調べたと
ころ、異物の大きさが原反の厚みの1/3以下の大きさ
であれば穴あきの発生しないことを見出した。そこでこ
の結果にノ^すいて、従来100gmの厚みの原反をカ
レンダー法により製造していたのを、各々50gmの厚
みでカレンダー成形した後、2枚を重合(タブリング)
し、 100gmの厚みのものとして延伸したところ、
穴あきが殆んど発生しなくなるという驚くべき結果のも
たらされることを確認し、この発明に到達したものであ
る。Based on theory 1j1, the present inventor investigated the relationship between the thickness of the original fabric of the perforated defective stretched film 11 and the size of foreign particles, and found that the size of the foreign particles was 1/3 or less of the thickness of the original fabric. It was found that if this was the case, no holes would occur. Based on this result, we used the calender method to produce original fabrics with a thickness of 100gm, but after calendering them to a thickness of 50gm, we polymerized the two sheets (tabbing).
When it was stretched to a thickness of 100 gm,
This invention was arrived at after confirming that the surprising result of almost no occurrence of holes was produced.
つぎに、この発明の詳細をその重合工程を示す添付図面
に基いて説明する0図においてl、 1は重合するため
の成形済み樹脂シート、 2.2はそれぞれの巻き戻し
ロールである。この重合に供される樹脂シー)1.1の
組合せとしては、ふっそ樹脂と塩化ビニル樹脂、アクリ
ル樹脂と塩化ビニル樹脂、塩化ビニル樹脂同志、ふっそ
樹脂同志、アクリル樹脂同志、塩酢ビ共重合体樹脂と塩
化ビニル樹脂、°塩酢ビ共用合体樹脂同志などが例示さ
れ、またこれらの樹脂シートの厚みの組合せとしては、
前述した厚みの1/3以[−の異物に起因する裂けを防
11−するために、一方のシートの最大の厚みが重合後
の全体の厚みの90%以下、好ましくは67%(2/3
)以ドとするのが適当である。67〜90%では厚いシ
ートの方に異物があってもfJiいシートの方が裂け、
破れの成長を阻止するストッパーとしての役;13を果
す、なお、重合に供する樹脂シートは図示のようなロー
ルに巻き取らずに、Tダイまたはカレンターで成形され
た直後のシートを直接重合工程に導入してもよく、また
重合する樹脂シートの枚数、樹脂の種類も2種以ヒ任、
aに選択することができる。Next, the details of this invention will be explained based on the accompanying drawings showing the polymerization process. In Figure 0, 1 and 1 are molded resin sheets for polymerization, and 2 and 2 are respective unwinding rolls. The combinations of resin sheets (1.1) to be subjected to this polymerization include fusso resin and vinyl chloride resin, acrylic resin and vinyl chloride resin, vinyl chloride resins together, fusso resins together, acrylic resins together, and salt and vinyl acetate resin together. Examples include polymer resins, vinyl chloride resins, and salt-vinyl-acetate combination resins, and combinations of the thicknesses of these resin sheets include:
In order to prevent tearing due to foreign matter of 1/3 or more of the above-mentioned thickness, the maximum thickness of one sheet should be 90% or less, preferably 67% (2/2) of the total thickness after polymerization. 3
) is appropriate. At 67% to 90%, even if there is a foreign object on the thicker sheet, the thinner sheet will tear,
Acts as a stopper to prevent the growth of tears; Note that the resin sheet to be subjected to polymerization is not wound up on a roll as shown in the figure, but the sheet immediately after being formed with a T-die or calendarer is directly subjected to the polymerization process. The number of resin sheets to be polymerized and the type of resin can also be changed to two or more types.
A can be selected.
巻き戻しロール2.2の各樹脂シート1,1はp240
−ル3,3で予熱された後、エキスパンターロール4.
4を経てドラムロール5に導かれて熱圧着により合着さ
れて一体のもの6となり、はがしロール7を経て、再び
ヒーター8によって加熱され、ゴムロール3とエンボス
ロールlOの間を通って、延伸工程へ送られる。Each resin sheet 1, 1 of the unwinding roll 2.2 is p240
- Expander roll 4.
4, it is led to a drum roll 5, where it is bonded by thermocompression bonding to form a single piece 6, which passes through a peeling roll 7, is heated again by a heater 8, passes between the rubber roll 3 and the embossing roll 1O, and then undergoes a stretching process. sent to.
この熱圧着の条件としては各樹脂シートの熱変形温度、
例えば、アクリル樹脂では74〜113℃、スチレン樹
脂では82〜115℃、ABS樹脂では77〜120℃
、プロピレン樹脂では100〜130℃、塩化ビニル樹
脂では100〜120℃、ふっそ樹脂では120℃など
にそれぞれ20〜50℃を加えた温度下で行なわれる。The conditions for this thermocompression bonding are the heat deformation temperature of each resin sheet,
For example, 74-113℃ for acrylic resin, 82-115℃ for styrene resin, 77-120℃ for ABS resin.
The heating is carried out at a temperature of 100 to 130°C for propylene resin, 100 to 120°C for vinyl chloride resin, 120°C for fluoride resin, and 20 to 50°C, respectively.
本発明における樹脂シートの重合に際しては、図示の熱
圧着に限定されるものではなく、接着剤または溶剤を用
いる接着であってもよい、これに用いられる接着剤は適
用される樹脂シートの種類により異なるが、塩酢ビ共重
合体、合成ゴムにトリルフェノール系)、ウレタン系、
ポリメチルメタクリレート系(例えばエポキシ828:
デュポン礼装商品名、ふっそ樹脂シート用)などのもの
が挙げられる。The polymerization of the resin sheet in the present invention is not limited to the thermocompression bonding shown in the figure, but may also be bonded using an adhesive or a solvent. Although different, salt-vinyl acetate copolymer, synthetic rubber (tolylphenol type), urethane type,
Polymethyl methacrylate (e.g. epoxy 828:
Examples include products such as DuPont formal dress product name (for Fusso resin sheets).
重合シートの延伸は引取りロール(2〜3本以」−1通
常は5〜6本以上で構成される)の引取速度を、ドラム
ロール5、エンボスロールlO、ゴムロール8などの回
転速度よりも高めることにより行なわれる。この延伸倍
率は105〜500%、&fましくは150〜300%
である。 105%未満ではシートの配向性、耐熱性
、熱収縮性、密着性等の向上のような延伸による効果が
望めず、また500%以1−ではシートに偏肉、片伸び
、波打ち等の現象を起し、シートの表面特性の低下、と
くには印刷時のムラ、ズレ、インキ溜りの発生などをも
たらす。The stretching of the polymerized sheet is performed by setting the take-up speed of the take-up rolls (usually composed of 5-6 rolls or more) to be higher than the rotational speed of the drum roll 5, embossing roll IO, rubber roll 8, etc. It is done by increasing. This stretching ratio is 105 to 500%, preferably 150 to 300%
It is. If it is less than 105%, no effects of stretching such as improvement of sheet orientation, heat resistance, heat shrinkability, adhesion, etc. can be expected, and if it is more than 500%, phenomena such as uneven thickness, one-sided elongation, and waving may occur in the sheet. This causes deterioration of the surface properties of the sheet, especially unevenness, misalignment, and the formation of ink pools during printing.
一力、延伸速度は線速で15〜100m/分で行なわれ
る。 100m/分を超えると、異物の存在するとこ
ろは勿論、シート自体の伸びが追いつかないので異物の
存在しない部分からも亀裂を生じ易くなり、延伸工程で
たとえ補助的にヒーターなどの外部加熱手段を併用した
としても加熱ムラを生じ易く、その結果としてシートの
片伸び、偏肉、亀裂を生じ易くなる。また、15m/分
より小さいと、シートの配向性向り効果がないのでシー
トの引張強度の向にがなく、またシート側縁部とシート
中央部との温度ムラのためにロールとの密着性について
側縁部と中央部とで差を生じ、これに起因して波打ち現
象、スティックスリップ(いわゆるキャーマーク)、シ
ートの折れなどができ易く、これを防止するために、た
とえ前述したような外部加熱手段を用いてシートを加温
したとしてもシートが分解し易く、ヤケの発生や色調変
化を来すことになる。The stretching is carried out at a linear speed of 15 to 100 m/min. If the speed exceeds 100 m/min, cracks are likely to occur not only in areas where foreign substances are present, but also in areas where foreign substances are not present, as the sheet itself cannot stretch as quickly as possible. Even if they are used together, uneven heating tends to occur, and as a result, the sheet tends to elongate on one side, have uneven thickness, and crack. If the speed is less than 15 m/min, there will be no effect on sheet orientation, so the tensile strength of the sheet will not be the same, and the adhesion to the roll will be affected due to temperature unevenness between the side edges of the sheet and the center of the sheet. There is a difference between the side edges and the center, which tends to cause waving, stick-slip (so-called car marks), and folding of the sheet. Even if the sheet is heated using some means, the sheet is likely to decompose, resulting in fading and color change.
次に、本発明を実施例により説IJIする。Next, the present invention will be explained using examples.
実施例1〜3、比較例1〜2
ポリ塩化ビニルとしてTK700 (信越化学工業社
製、商品名)100重¥81S(以ド同じ)、熱安定剤
としてLS−140(昭島化学社製、商品名、メルカプ
ト錫系)2部、可塑剤としてジオクチルフタレートを5
部、滑剤としてCa−3tを0.5部とステアリン酸0
.5部、および顔料としてR−9867(大11精化製
、Co系顔料)5部からなる塩化ビニル樹脂を、Tダイ
成形法、カレンダー成形法によってそれぞれ下表に示す
厚みの960m1巾のシートIおよび11に成形してロ
ールに巻取った。これを第1図に示した装置を用いて速
度15m/分、温度160〜180℃でシー)1と11
を重合し、熱圧着した後、延伸倍*250%、延伸速度
50m/分で延伸し、 945mm巾の延伸フィルムを
11)た、各延伸フィルムについての1ooo+s当り
の米粒大息」−の穴あき個数の検査結果を下表に併記し
た。Examples 1 to 3, Comparative Examples 1 to 2 TK700 (manufactured by Shin-Etsu Chemical Co., Ltd., trade name) 100 weight ¥81S (same hereafter) as polyvinyl chloride, LS-140 (manufactured by Akishima Chemical Co., Ltd., product) as a heat stabilizer 2 parts of mercaptotin series), 5 parts of dioctyl phthalate as a plasticizer
part, 0.5 part of Ca-3t as a lubricant and 0 part of stearic acid.
.. and 5 parts of R-9867 (manufactured by Dai-11 Seika Co., Ltd., Co-based pigment) as a pigment, were made into a 960 m1-wide sheet I with the thickness shown in the table below by the T-die molding method and the calendar molding method, respectively. and 11 and wound up into a roll. This was carried out using the apparatus shown in Figure 1 at a speed of 15 m/min and a temperature of 160 to 180°C.) 1 and 11
After polymerizing and thermo-compression bonding, the film was stretched at a stretching ratio of 250% and a stretching speed of 50 m/min to form a stretched film with a width of 945 mm. Each stretched film had holes of the size of rice grains per 100+s. The inspection results for the number of pieces are also listed in the table below.
表
樹脂中の異物の大きさは径30gm以北のものであった
が、本発明の方法による延伸フィルムではU物の存在場
所で一方のシート層で穴開きを起しても、他方のシート
層で完全に防止されたため、穴開き個数は合格ライン内
に抑えられていた。The size of the foreign matter in the surface resin was 30 gm or more in diameter, but in the stretched film according to the method of the present invention, even if holes were formed in one sheet layer at the location where the U material was present, the other sheet layer The number of holes was kept within the passing line because the layer completely prevented them.
(発明の効果)
1、 H伸フィルム製造時における穴開き不良が無く
なるため、製品の歩留りが大巾に向とする。(Effects of the invention) 1. Since the hole punching defects during the production of H-stretched film are eliminated, the yield of the product is greatly improved.
2、 カレンダー成形における原反の製造およびこれか
らの延伸フィルムの製造が容易となり、歩留の向上が図
れる。2. Production of the original film in calendar molding and subsequent production of stretched film is facilitated, and the yield can be improved.
3、異種の樹脂シートや厚みの異なる樹脂シートを、適
宜組合せることにより、延伸倍率が一定で、各樹脂の特
徴を生かし、また任意の厚みを有する延伸フィルムの製
造が回旋となる。3. By appropriately combining different types of resin sheets or resin sheets with different thicknesses, a stretched film with a constant stretching ratio, taking advantage of the characteristics of each resin, and having an arbitrary thickness can be produced by spinning.
4、成形、重合、延伸の各工程のインライン化が可能と
なり、製造プロセスの合理化が図れる。4. Each process of molding, polymerization, and stretching can be done in-line, streamlining the manufacturing process.
5、従来、原反中が広がる程、穴あき不良率も増加して
いたのが本発明の方法では巾が広がってもそれ程不良率
が増加せず、従って広巾のシートに対して特に有効であ
る。5. Conventionally, as the width of the original sheet spread, the defective rate due to holes increased, but with the method of the present invention, the defective rate does not increase that much even when the width increases, so it is particularly effective for wide sheets. be.
6、異物混入機会の多いカレンダー成形や高充填剤配合
または高顔料配合のシート成形において穴開きが防止で
きるためとくに有用である。6. It is particularly useful because it can prevent holes in calender molding and sheet molding with high filler or pigment content, where there is a high chance of contamination by foreign matter.
図面は本発明における重合工程を示す説明図である。 #4F許出穎人 信越ポリマー株式会社第1図 6合着シート ! The drawings are explanatory diagrams showing the polymerization process in the present invention. #4F Keijin Shin-Etsu Polymer Co., Ltd. Figure 1 6-piece sheet !
Claims (1)
延伸することを特徴とする延伸フィルムの製造方法。1. After stacking and bonding two or more layers of formed original fabric,
A method for producing a stretched film, which comprises stretching.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18646586A JPS6342837A (en) | 1986-08-08 | 1986-08-08 | Manufacture of oriented film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18646586A JPS6342837A (en) | 1986-08-08 | 1986-08-08 | Manufacture of oriented film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6342837A true JPS6342837A (en) | 1988-02-24 |
Family
ID=16188943
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18646586A Pending JPS6342837A (en) | 1986-08-08 | 1986-08-08 | Manufacture of oriented film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6342837A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5131775A (en) * | 1974-09-12 | 1976-03-18 | Matsushita Electric Ind Co Ltd | GOKUHAKUPURASUCHITSUKUFUIRUMU NO SEIZOHOHO |
JPS51132288A (en) * | 1975-05-14 | 1976-11-17 | Toray Ind Inc | Stretched, thick polypropylene film |
JPS52105972A (en) * | 1976-03-03 | 1977-09-06 | Matsuki Masamichi | Method of manufacturing laminated elongation film |
JPS5374578A (en) * | 1976-12-14 | 1978-07-03 | Mitsubishi Plastics Ind | Method for making laminated film |
-
1986
- 1986-08-08 JP JP18646586A patent/JPS6342837A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5131775A (en) * | 1974-09-12 | 1976-03-18 | Matsushita Electric Ind Co Ltd | GOKUHAKUPURASUCHITSUKUFUIRUMU NO SEIZOHOHO |
JPS51132288A (en) * | 1975-05-14 | 1976-11-17 | Toray Ind Inc | Stretched, thick polypropylene film |
JPS52105972A (en) * | 1976-03-03 | 1977-09-06 | Matsuki Masamichi | Method of manufacturing laminated elongation film |
JPS5374578A (en) * | 1976-12-14 | 1978-07-03 | Mitsubishi Plastics Ind | Method for making laminated film |
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