JPH03269103A - Gloves made of plastic film - Google Patents
Gloves made of plastic filmInfo
- Publication number
- JPH03269103A JPH03269103A JP2065788A JP6578890A JPH03269103A JP H03269103 A JPH03269103 A JP H03269103A JP 2065788 A JP2065788 A JP 2065788A JP 6578890 A JP6578890 A JP 6578890A JP H03269103 A JPH03269103 A JP H03269103A
- Authority
- JP
- Japan
- Prior art keywords
- ethylene
- gloves
- plastic film
- density
- film
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000002985 plastic film Substances 0.000 title claims description 17
- 229920006255 plastic film Polymers 0.000 title claims description 17
- 239000004711 α-olefin Substances 0.000 claims abstract description 18
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 13
- 229920001684 low density polyethylene Polymers 0.000 claims abstract description 7
- 239000004702 low-density polyethylene Substances 0.000 claims abstract description 7
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims abstract description 5
- 229920005989 resin Polymers 0.000 claims abstract description 3
- 239000011347 resin Substances 0.000 claims abstract description 3
- 210000000707 wrist Anatomy 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 3
- 238000003466 welding Methods 0.000 claims description 3
- 229920006226 ethylene-acrylic acid Polymers 0.000 claims description 2
- 229920000554 ionomer Polymers 0.000 claims description 2
- 238000010030 laminating Methods 0.000 claims description 2
- 239000011342 resin composition Substances 0.000 claims description 2
- 238000004049 embossing Methods 0.000 abstract description 12
- 239000002341 toxic gas Substances 0.000 abstract description 2
- 238000002156 mixing Methods 0.000 abstract 1
- 239000012808 vapor phase Substances 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- 239000005977 Ethylene Substances 0.000 description 6
- 238000004851 dishwashing Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- -1 dodecene-1 Chemical compound 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 210000004247 hand Anatomy 0.000 description 2
- 239000000203 mixture Chemical group 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 230000035807 sensation Effects 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- 239000002879 Lewis base Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000007527 lewis bases Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 238000003825 pressing Methods 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
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
Landscapes
- Gloves (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、製造が容易で、しかも性能の優れたプラスチ
ックフィルム製手袋に関し、さらに詳しくは、台所、工
場、結婚式場、ホテル、病院、塗装現場、実験室、食料
品店等の種々の場所で簡易に使用され、使い捨てできる
特定のポリエチレン系樹脂で製造したプラスチックフィ
ルム製手袋に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to gloves made of plastic film that are easy to manufacture and have excellent performance. This invention relates to plastic film gloves made of a specific polyethylene resin that can be easily used and disposable in various places such as workplaces, laboratories, and grocery stores.
従来、使い捨てプラスチックフィルム製手袋としては、
塩ビフィルム、高圧法低密度ポリエチレンフィルムまた
はエチレン−酢酸ビニル共重合体フィルム等を2枚重ね
合わせて、手形に合わせ外周をヒートシールで溶着した
ものが、低価格で、使用が簡便なため、主として使用さ
れている。Conventionally, disposable plastic film gloves were
PVC film, high-pressure low-density polyethylene film, or ethylene-vinyl acetate copolymer film, etc., are stacked together and the outer periphery is heat-sealed to fit the shape of the hand.Because they are inexpensive and easy to use, they are mainly used. It is used.
しかしながら、塩ビフィルムは塩素を含んでいるので、
焼却すると環境を汚染し、高圧法低密度ポリエチレンフ
ィルムはヒートシール強度が低く、溶着部に力が加わる
と破れやすく、柔軟性に欠け、モしてエチレン−酢酸ビ
ニル共重合体フィルムは同様にヒートシール強度が十分
でなく、ブロッキング性があり、使用時手首部分の口開
きが悪く、さらにコストが高い等の問題があった。However, since PVC film contains chlorine,
Incineration pollutes the environment, high-pressure low-density polyethylene film has low heat-sealing strength, tends to tear when force is applied to the welded area, and lacks flexibility; There were problems such as insufficient sealing strength, blocking properties, poor opening at the wrist during use, and high cost.
そこで本発明は従来のプラスチックフィルム製手袋が有
する上記問題点を解消し、コストが低く、ヒートシール
した溶着部の強度が強く、さらに製造後の感触がよく、
柔軟性があり、ブロッキング現象を起こさず、しかも焼
却時有毒なガスを発生しないプラスチックフィルム製手
袋を提供することを目的とする。Therefore, the present invention solves the above-mentioned problems of conventional plastic film gloves, is low in cost, has strong heat-sealed welded parts, and has a good feel after manufacturing.
To provide a plastic film glove that is flexible, does not cause a blocking phenomenon, and does not generate toxic gas when incinerated.
本発明者等は鋭意研究の結果、従来使用されていた塩ビ
、高圧法低密度ポリエチレンまたはエチレン−酢酸ビニ
ル共重合体等に代えて、近年開発された気相法で製造さ
れた密度が06910g/ml以下の低密度エチレン−
α−オレフィン共重合体を検討し、これがプラスチック
フィルム製手袋の材料として優れた性質を有することを
見出し、本発明を完成した。As a result of intensive research, the inventors of the present invention found that the density of 0.6910 g / Low density ethylene less than ml
The inventors studied α-olefin copolymers and found that they have excellent properties as a material for plastic film gloves, and completed the present invention.
すなわち本発明は、気相低圧法で製造された密度が0.
910g/ml以下である直鎖状エチレン−α−オレフ
ィン共重合体からなるフィルムを2枚重ね合わせ、手形
に合わせて外周を熱溶着し、手首部分を開放口としたプ
ラスチックフィルム製手袋に関する。That is, in the present invention, the density of the product manufactured by the gas phase low pressure method is 0.
The present invention relates to a plastic film glove made by laminating two films made of a linear ethylene-α-olefin copolymer having a weight of 910 g/ml or less, heat-welding the outer periphery to fit the hand shape, and having an open opening at the wrist.
ここで、直鎖状エチレン−α−オレフィン共重合体は単
独で使用されても、2種以上混合して使用されてもよい
。Here, the linear ethylene-α-olefin copolymer may be used alone or in combination of two or more types.
また本発明において、フィルムの片面または両面がエン
ボス加工され、その深さが2ないし300μであるプラ
スチックフィルム製手袋が好ましい。Further, in the present invention, it is preferable to use a plastic film glove which is embossed on one or both sides of the film and has a depth of 2 to 300 μm.
さらに、本発明において、上記の気相低圧法で製造され
た密度が0.910 g/s+/以下である直鎖状エチ
レン−α−オレフィン共重合体100重量部に対して、
高圧法低密度ポリエチレン、エチレン−酢酸ビニル共重
合体、エチレン−アクリル酸エステル共重合体およびア
イオノマーからなる群から選択される1種または2種以
上の樹脂を0ないし900重量部さらに配合した樹脂組
成物から製造したフィルムを使用してなるプラスチック
フィルム製手袋も好ましい。ここで配合される直鎖状エ
チレン−α−オレフィン共重合体以外の成分の量は、こ
の直鎖状エチレン−α−オレフィン共重合体の特徴をを
損なわない範囲で選択される。Furthermore, in the present invention, for 100 parts by weight of the linear ethylene-α-olefin copolymer having a density of 0.910 g/s+/ or less produced by the above gas phase low pressure method,
A resin composition further containing 0 to 900 parts by weight of one or more resins selected from the group consisting of high-pressure low-density polyethylene, ethylene-vinyl acetate copolymer, ethylene-acrylic acid ester copolymer, and ionomer. Also preferred are plastic film gloves made from a film made from a plastic film. The amount of components other than the linear ethylene-α-olefin copolymer blended here is selected within a range that does not impair the characteristics of the linear ethylene-α-olefin copolymer.
本発明において、気相低圧法で製造された密度が0.9
10g/ml以下である直鎖状エチレン−a−オレフィ
ン共重合体とは、エチレン20ないし70重量%とα−
オレフィン80ないし301量%とから、好ましくはエ
チレン40ないし60重量%とα−オレフィン60ない
し40重量%とからなるものである。In the present invention, the density produced by the gas phase low pressure method is 0.9
A linear ethylene-a-olefin copolymer having a concentration of 10 g/ml or less means 20 to 70% by weight of ethylene and α-
It consists of 80 to 301% by weight of olefins, preferably 40 to 60% by weight of ethylene and 60 to 40% by weight of α-olefins.
本明細書においてα−オレフィンとは炭素原子数3ない
し12のものを意味し、直鎖状であっても分岐状であっ
てもよく、例えばプロピレン、ブテン−11ヘキセン−
11へブテン−1、オクテンーエ、ノネン−1、デセン
−1、ウンデセン−1、ドデセン−1,4メチルペンテ
ン1.4−メチルヘキセン−1,4,4−ジメチルペン
テン−1等が包含される。In this specification, α-olefin means one having 3 to 12 carbon atoms, and may be linear or branched, such as propylene, butene-11hexene-
11-hebutene-1, octene-1, nonene-1, decene-1, undecene-1, dodecene-1,4-methylpentene, 1,4-methylhexene-1,4,4-dimethylpentene-1, and the like.
本発明で使用される密度が0.910g/ml以下の直
鎖状エチレン−α−オレフィン共重合体は以下のような
連続的製造方法で製造されることが好ましい:
流動床反応帯域中、IOないし80℃の温度かつ700
0KP&以下の圧力で、
+al 高級α−オレフィン:エチレンのモル比が0
.35:lないし8.0:1である、エチレンおよび炭
素原子数3ないし12の少なくとも1種の高級α−オレ
フィンと、
(bl 少なくとも25モル%の少なくとも1種の希
釈ガス、
とを含有する気体混合ガスを、
次式■:
Mg、Ti (OR)、X、[ED]、(I)(式中、
Rは炭素原子数1ないし14の脂肪族もしくは芳香族炭
化水素基または基COR’ を表し、Roは炭素原子数
1ないし14の脂肪族もしくは芳香族炭化水素基を表し
、
Xは塩素原子、臭素原子、ヨウ素原子およびその混合物
からなる群から選択され、
EDは脂肪族もしくは芳香族酸のアルキルエステル、脂
肪族エーテル、環式エーテルおよび脂肪族ケトンからな
る群から選択される有機電子供与化合物を表し、
mは0.5ないし56であり、
nは0、■または2であり、
pは2ないし116であり、
qは2ないし85である6)
で表される先駆体組成物からなる触媒系の粒子と連続的
に接触させ、前記先駆体組成物を不活性キャリア材料で
希釈すると共に、次式■:Al (R’)、X’、H,
(ff)
(式中、
X゛は塩素原子または基OR’を表し、RoおよびR”
は互いに独立して炭素原子数1ないし14の飽和炭化水
素基を表し、eは0ないし1.5であり、
fは0またはlであり、
d+e+f=3である。)
で表される有機アルミニウム化合物で完全に活性化させ
る方法。ただし上記活性化化合物は前記反応帯域中おけ
る全アルミニウム:チタンのモル比が10:1ないし4
00:1となるような量で使用される。この製法に関す
る詳細は特開昭59−230011号に記載されている
。The linear ethylene-α-olefin copolymer having a density of 0.910 g/ml or less used in the present invention is preferably produced by the following continuous production method: In a fluidized bed reaction zone, IO Temperature between 80℃ and 700℃
At pressures below 0 KP and +al, the molar ratio of higher α-olefin: ethylene is 0.
.. 35:1 to 8.0:1 of ethylene and at least one higher α-olefin having from 3 to 12 carbon atoms; and (bl at least 25 mol %) at least one diluent gas. The mixed gas is represented by the following formula: Mg, Ti (OR), , Ro represents an aliphatic or aromatic hydrocarbon group having 1 to 14 carbon atoms, X is selected from the group consisting of chlorine atom, bromine atom, iodine atom and mixtures thereof, and ED is an aliphatic or aromatic acid represents an organic electron donating compound selected from the group consisting of alkyl esters, aliphatic ethers, cyclic ethers, and aliphatic ketones, m is 0.5 to 56, n is 0, ■, or 2, p is from 2 to 116, and q is from 2 to 85. 6) diluting said precursor composition with an inert carrier material. In addition, the following formula ■: Al (R'), X', H,
(ff) (In the formula, X'' represents a chlorine atom or a group OR', and Ro and R''
independently represent a saturated hydrocarbon group having 1 to 14 carbon atoms, e is 0 to 1.5, f is 0 or l, and d+e+f=3. ) A method of complete activation with an organoaluminum compound represented by provided that the activating compound has a total aluminum:titanium molar ratio in the reaction zone of 10:1 to 4.
00:1. Details regarding this manufacturing method are described in JP-A-59-230011.
これとは別に本発明の直鎖状エチレン−αオレフィン共
重合体は以下のように製造されてもよい:
エチレンと少なくとも1種の炭素原子数3ないし12の
α−オレフィンとを気相中で約1゜℃ないし約115℃
の温度において、
(A) (1)塩素、臭素またはヨウ素による三ハロゲ
ン化バナジウムta+と、該三ハロゲン化バナジウムが
可溶である液状の有機ルイス塩基である電子供与体(b
lとの反応生成物であるバナジウム化合物と、
(2)次式■:
MX、 (III)
(式中、
Mはホウ素原子または基A I R+3−1+を表し、
各Rはそれぞれアルキル基を表すが、
ただしいずれのR基においても炭素原子の総数は14を
越えず、
Xは塩素原子、臭素原子またはヨウ素
原子を表し、
aは0、lまたは2であり、ただしM
がホウ素原子を表すときaは3である。)で表される変
性剤、
とをシリカまたはアルミナから実質的になる固体不活性
担体上に担持させたものから実質的になる担持された先
駆物質と、
<8>次式■:
AiR,(IV)
(式中、Rは式■の定義と同じ意味を表す。Alternatively, the linear ethylene-α-olefin copolymers of the invention may be prepared as follows: ethylene and at least one C3-C12 α-olefin are combined in a gas phase. Approximately 1°C to approximately 115°C
At a temperature of (A) (1) vanadium trihalide ta+ with chlorine, bromine or iodine and an electron donor (b) which is a liquid organic Lewis base in which the vanadium trihalide is soluble;
(2) The following formula ■: MX, (III) (wherein M represents a boron atom or a group A I R + 3-1 +, and each R represents an alkyl group) However, the total number of carbon atoms in any R group does not exceed 14, X represents a chlorine atom, bromine atom or iodine atom, a is 0, l or 2, provided that when M represents a boron atom a is 3); and a supported precursor material consisting essentially of a solid inert support consisting essentially of silica or alumina; Formula ■: AiR, (IV) (In the formula, R represents the same meaning as the definition of Formula ■.
)で表される助触媒と、
(C)次式V:
R’、CX’+、、+ (V)
(式中、
R1は水素原子または非置換もしくはハロゲン置換され
た低級アルキル基を表し、XI はハロゲン原子を表し
、
bは0、lまたは2である。)
で表される促進剤、
を含む触媒組成物と接触させる方法。この方法の詳細は
特開昭59−23006号に記載されている。), and (C) the following formula V: R', CX'+,, + (V) (wherein R1 represents a hydrogen atom or an unsubstituted or halogen-substituted lower alkyl group, XI represents a halogen atom, and b is 0, 1 or 2. Details of this method are described in JP-A-59-23006.
本発明に使用するフィルムは、インフレーションチュー
ブラ−フィルム製造法、Tダイキャスト法で製造し、必
要に応じてフィルムの片面または両面にエンボス加工を
施す。The film used in the present invention is manufactured by a blown tubular film manufacturing method or a T-die casting method, and embossing is applied to one or both sides of the film as necessary.
フィルムの厚さは10ないし200μ、好ましくは20
ないし100μである。これは、10μ未満であるとフ
ィルムが破れやすく、200μを越えると作業性が悪く
なり、製造コストが高くなることによる。The thickness of the film is between 10 and 200μ, preferably 20μ
The thickness is between 100μ and 100μ. This is because if the thickness is less than 10μ, the film will be easily torn, and if it exceeds 200μ, workability will deteriorate and manufacturing costs will increase.
エンボス加工は適当な表面粗度を有するチルロールとプ
レッシャーロールとの間でフィルムを加圧し、該フィル
ムの片面または両面に施すものである。エンボス加工を
施すことにより、フィルムの外観が美しくなり、商品価
値が向上するばかりでなく、手袋として使用する時、表
面の凹凸により物体をつかみやすくなり、またフィルム
同志のブロッキングを防止する効果がある。Embossing is applied to one or both sides of a film by pressing the film between a chill roll and a pressure roll having an appropriate surface roughness. Embossing not only gives the film a beautiful appearance and improves its commercial value, but when used as gloves, the uneven surface makes it easier to grip objects and prevents the films from blocking each other. .
エンボスの種類には、亀甲、格子、絹目、ダイヤ、玉虫
、麻目、梨地、しぶき等があり、これらの全てが有効で
あるが、エンボス深さ(JIs BO601に準拠し
て測定)は、2ないし300μ、好ましく5ないし20
0μである。Types of embossing include tortoiseshell, lattice, silk, diamond, bead, linen, satin, and splash, and all of these are effective, but the embossing depth (measured in accordance with JIs BO601) is 2 to 300 μ, preferably 5 to 20
It is 0μ.
これは、2μ未満であると上記の効果を示さず、300
μを越えるとヒートシール性が悪くなり、また外観も粗
雑な感じを与え望ましくないことによる。This does not show the above effect when it is less than 2μ, and 300μ
If it exceeds .mu., the heat sealability will be poor and the appearance will be undesirably rough.
本発明のプラスチックフィルム製手袋は以下のように製
造する・
フィルムをインフレーション法またはTダイ法により製
造し、その表面を必要に応じてエンボス加工する。The plastic film glove of the present invention is manufactured as follows: A film is manufactured by an inflation method or a T-die method, and its surface is embossed as necessary.
次に、2枚のフィルムを重ねた後、手形の外周をヒート
シールして熱溶着し、熱溶着部の外側を切断し、手袋と
する。ここで熱溶着と切断を同時に行う、いわゆる熱溶
断を行ってもよい。Next, after overlapping the two films, the outer periphery of the handprint is heat-sealed and welded, and the outside of the heat-welded part is cut to form a glove. Here, thermal welding and cutting may be performed simultaneously, so-called thermal cutting.
なお、手首部分は予め残して熱溶着して開放口としても
よいが、手形外周全てを熱溶着し、使用時にハサミで切
断して開放口とすることもできる。Note that the wrist portion may be left in advance and thermally welded to form an open opening, but it is also possible to thermally weld the entire periphery of the hand and cut it with scissors during use to form an open opening.
実施例1
密度0.906g/+1/、メルトインデックス0.8
g/10分のエチレン−ブテン−1共重合体(ユニオン
カーバイト社製、DFDA−1137)を用いてTダイ
法により厚さ70μのフィルムを製造し、これを2枚重
ね合わせた後、手形の外周部分を手首部分を残して幅2
■で熱溶着し、その外側をハサミで切断し、プラスチッ
クフィルム製手袋を10枚製造した。Example 1 Density 0.906g/+1/, melt index 0.8
A film with a thickness of 70 μm was produced by the T-die method using an ethylene-butene-1 copolymer (manufactured by Union Carbide Co., Ltd., DFDA-1137) of 1 g/10 minutes, and after overlapping two films, a bill was formed. The width of the outer periphery is 2, leaving the wrist part.
The gloves were thermally welded using Step (3) and the outside was cut with scissors to produce 10 plastic film gloves.
これを用いて1時間皿洗い作業を行ったが、ヒートシー
ルによる熱溶着部分の破断は100枚重において起こら
なかった。また、この手袋はゴム状の感触があり、手の
感覚がそのまま作業対iの皿に伝わるため、皿を落とし
て割るような事故は1件も発生しなかった。Dishwashing work was carried out using this for one hour, but no breakage of the thermally welded portion due to heat sealing occurred after 100 sheets were loaded. In addition, these gloves have a rubber-like feel, and the sensations of the hands are directly transmitted to the plate of work i, so there were no accidents such as dropping and breaking the plate.
実施例2
実施例1と同様なフィルムを製造し、この外面に200
μのエンボス深さのエンボス加工を行った以外は、実施
例1と同様の操作をして手袋を製造し、同様の試験を行
った。Example 2 A film similar to that of Example 1 was produced, and the outer surface was coated with 200
Gloves were manufactured in the same manner as in Example 1, except that the embossing was performed to an embossing depth of μ, and the same tests were conducted.
本実施例では表面にエンボス加工を施しであるため、実
施例1のものに比べさらに作業性が向上し、2時間皿洗
い作業を行っても皿を割る事故は1件も発生しなかった
。In this example, since the surface was embossed, the workability was further improved compared to that in Example 1, and even after washing dishes for 2 hours, there was no accident of breaking the dishes.
実施例3
実施例1と同様なフィルムを製造し、この両面に100
μのエンボス深さのエンボス加工を行った以外は、実施
例1と同様の操作をして手袋を製造し、同様の試験を行
った。Example 3 A film similar to Example 1 was produced, and 100% of the film was coated on both sides.
Gloves were manufactured in the same manner as in Example 1, except that the embossing was performed to an embossing depth of μ, and the same tests were conducted.
本実施例では両面にエンボス加工を施しであるため、実
施例1および2のものに比べ、手袋内面の手との感触が
よくなり、さらに作業性が向上し、3時間皿洗い作業を
行っても皿を割る事故は1件も発生しなかった。In this example, both sides are embossed, so the inner surface of the glove feels better against the hand than in Examples 1 and 2, and workability is further improved, even after washing dishes for 3 hours. There were no incidents of plates breaking.
実施例4
実施例1と同様なフィルムを製造し、この内面側に20
0μのエンボス深さのエンボス加工を行った以外は、実
施例1と同様の操作をして手袋を製造し、同様の試験を
行った。Example 4 A film similar to Example 1 was manufactured, and 20
Gloves were manufactured in the same manner as in Example 1, except that embossing with an embossing depth of 0 μ was performed, and the same tests were conducted.
本実施例では内面にエンボス加工を施しであるため、手
の出し入れが容易で、その感触がよく、手袋としてのソ
フト感が得られた。しかも作業性もよく、1時間皿洗い
作業を行っても皿を割る事故は1件も発生しなかった。In this example, since the inner surface was embossed, it was easy to put the hand in and take it out, and the glove had a good feel and a soft feel as a glove. Moreover, it was easy to work with, and even after washing dishes for an hour, there were no incidents of breaking dishes.
比較例1
フィルムの材料として高圧法低密度ポリエチレン(密度
0.920 g/a/、メルトインデックス1.3g/
10分1日本ユニカー製、DND−2450)を用いた
以外は、実施例1と同様の操作を行い手袋を製造し、同
様に試験を行った。Comparative Example 1 High pressure low density polyethylene (density 0.920 g/a/, melt index 1.3 g/
Gloves were produced in the same manner as in Example 1, except that 10 minutes (manufactured by Nippon Unicar, DND-2450) were used, and the tests were conducted in the same manner.
この手袋の熱溶着部の強度は弱く、1時間の皿洗い作業
で10枚中9枚が破れた。また、手袋の感触がごわごわ
した感じで、手の感覚が作業対照の皿に伝わらず、上記
作業時間中5枚の皿の落下事故が発生した。The strength of the heat-welded parts of these gloves was weak, and 9 out of 10 gloves were torn after 1 hour of washing dishes. In addition, the gloves felt stiff and the sensation of the hand was not transmitted to the plate being used as a control, and five plates were accidentally dropped during the above-mentioned working time.
比較例2
エチレン−酢酸ビニル共重合体(密度0.935 g/
m1.酢酸ビニル含量10%、メルトインデックス1.
3g/10分1日本ユニカー製、DQDJ−1830)
を用いた以外は、実施例1と同様の操作を行い手袋を製
造し、同様に試験を行った。Comparative Example 2 Ethylene-vinyl acetate copolymer (density 0.935 g/
m1. Vinyl acetate content 10%, melt index 1.
3g/10min 1 Nippon Unicar, DQDJ-1830)
Gloves were manufactured in the same manner as in Example 1, except that the gloves were used, and the tests were conducted in the same manner.
この手袋は比較例1の高圧法低密度ポリエチレンを用い
たものよりは熱溶着部強度が強く、作業性はよかったが
、1時間の皿洗い作業でlO枚中5枚が破れ、3枚の皿
の落下事故が発生した。These gloves had stronger heat-welded parts and better workability than Comparative Example 1, which used high-pressure low-density polyethylene, but 5 out of 10 gloves were torn after 1 hour of dishwashing work, and 3 plates were washed. A fall accident occurred.
本発明のプラスチックフィルム製手袋は、ゴムの性質に
近い特定のエチレン−α−オレフィン共重合体フィルム
を素材として使用しているので、ヒートシール部が破損
することなく、手の感覚が作業対象にそのまま伝わり、
非常に作業性がよい。また、表面にエンボス加工を施し
たフィルムを使用したものは、手との感触が高まり、そ
して対象物との接触性がよくなり、作業性がさらに向上
する。The plastic film gloves of the present invention use a specific ethylene-α-olefin copolymer film with properties close to rubber as a material, so the heat-sealed part will not be damaged and the hands will feel more comfortable when working. It is transmitted as it is,
Very easy to work with. In addition, when using a film with an embossed surface, it feels better in the hand and has better contact with the object, further improving workability.
Claims (3)
l以下である直鎖状エチレン−α−オレフィン共重合体
からなるフィルムを2枚重ね合わせ、手形に合わせて外
周を熱溶着し、手首部分を開放口としたプラスチックフ
ィルム製手袋。(1) Density manufactured by gas phase low pressure method is 0.910 g/m
This plastic film glove is made by laminating two films made of a linear ethylene-α-olefin copolymer having a diameter of 1 or less and heat-welding the outer periphery to fit the hand shape, and having an open opening at the wrist.
その深さが2ないし300μである請求項1記載のプラ
スチックフィルム製手袋。(2) one or both sides of the film are embossed;
The plastic film glove according to claim 1, wherein the depth thereof is 2 to 300 microns.
l以下である直鎖状エチレン−α−オレフィン共重合体
100重量部に対して、高圧法低密度ポリエチレン、エ
チレン−酢酸ビニル共重合体、エチレン−アクリル酸エ
ステル共重合体およびアイオノマーからなる群から選択
される1種または2種以上の樹脂を0ないし900重量
部配合した樹脂組成物から製造したフィルムを使用して
なる請求項1記載のプラスチックフィルム製手袋。(3) Density manufactured by gas phase low pressure method is 0.910 g/m
From the group consisting of high-pressure low-density polyethylene, ethylene-vinyl acetate copolymer, ethylene-acrylic acid ester copolymer, and ionomer, per 100 parts by weight of a linear ethylene-α-olefin copolymer of 1 or less 2. The plastic film glove according to claim 1, which is made of a film produced from a resin composition containing 0 to 900 parts by weight of one or more selected resins.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2065788A JPH03269103A (en) | 1990-03-16 | 1990-03-16 | Gloves made of plastic film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2065788A JPH03269103A (en) | 1990-03-16 | 1990-03-16 | Gloves made of plastic film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03269103A true JPH03269103A (en) | 1991-11-29 |
Family
ID=13297124
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2065788A Pending JPH03269103A (en) | 1990-03-16 | 1990-03-16 | Gloves made of plastic film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03269103A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5160199A (en) * | 1989-12-06 | 1992-11-03 | Franco Berti | Halogen lamp reflector including a ceramic material paraboloid light reflecting element |
JP2002105252A (en) * | 2000-09-29 | 2002-04-10 | Sumitomo Chem Co Ltd | Polyethylene resin composition and low gloss polyethylene film |
JP2003055821A (en) * | 2001-08-09 | 2003-02-26 | Okamoto Ind Inc | Synthetic resin glove |
WO2013150759A1 (en) * | 2012-04-03 | 2013-10-10 | 信越化学工業株式会社 | Resin gloves |
CN103610245A (en) * | 2013-12-10 | 2014-03-05 | 唐山川欧森塑料制品有限公司 | PVC-class disposable glove and manufacturing technology thereof |
CN103720089A (en) * | 2013-12-10 | 2014-04-16 | 唐山川欧森塑料制品有限公司 | Method of producing disposable PVC gloves |
JP2018100460A (en) * | 2016-12-20 | 2018-06-28 | エフピコ商事株式会社 | Plastic film glove |
US20210345715A1 (en) * | 2020-05-06 | 2021-11-11 | Top Glove International Sdn. Bhd. | Embossments for thin film articles |
-
1990
- 1990-03-16 JP JP2065788A patent/JPH03269103A/en active Pending
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5160199A (en) * | 1989-12-06 | 1992-11-03 | Franco Berti | Halogen lamp reflector including a ceramic material paraboloid light reflecting element |
JP2002105252A (en) * | 2000-09-29 | 2002-04-10 | Sumitomo Chem Co Ltd | Polyethylene resin composition and low gloss polyethylene film |
JP2003055821A (en) * | 2001-08-09 | 2003-02-26 | Okamoto Ind Inc | Synthetic resin glove |
WO2013150759A1 (en) * | 2012-04-03 | 2013-10-10 | 信越化学工業株式会社 | Resin gloves |
JP2013213299A (en) * | 2012-04-03 | 2013-10-17 | Shin-Etsu Chemical Co Ltd | Resin-made glove |
CN103610245A (en) * | 2013-12-10 | 2014-03-05 | 唐山川欧森塑料制品有限公司 | PVC-class disposable glove and manufacturing technology thereof |
CN103720089A (en) * | 2013-12-10 | 2014-04-16 | 唐山川欧森塑料制品有限公司 | Method of producing disposable PVC gloves |
CN103610245B (en) * | 2013-12-10 | 2015-10-28 | 唐山川欧森塑料制品有限公司 | PVC kind disposable gloves and production technology thereof |
CN103720089B (en) * | 2013-12-10 | 2015-11-04 | 唐山川欧森塑料制品有限公司 | The production method of PVC kind disposable gloves |
JP2018100460A (en) * | 2016-12-20 | 2018-06-28 | エフピコ商事株式会社 | Plastic film glove |
US20210345715A1 (en) * | 2020-05-06 | 2021-11-11 | Top Glove International Sdn. Bhd. | Embossments for thin film articles |
US11969036B2 (en) * | 2020-05-06 | 2024-04-30 | Top Glove International Sdn. Bhd. | Embossments for thin film articles |
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