JPH03212435A - polyolefin resin film - Google Patents
polyolefin resin filmInfo
- Publication number
- JPH03212435A JPH03212435A JP801090A JP801090A JPH03212435A JP H03212435 A JPH03212435 A JP H03212435A JP 801090 A JP801090 A JP 801090A JP 801090 A JP801090 A JP 801090A JP H03212435 A JPH03212435 A JP H03212435A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- group
- film
- carbon atoms
- polyolefin resin
- 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.)
- Granted
Links
- 229920005672 polyolefin resin Polymers 0.000 title claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- -1 fatty acid ester Chemical class 0.000 claims description 11
- 239000000654 additive Substances 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 9
- 229930195729 fatty acid Natural products 0.000 claims description 9
- 239000000194 fatty acid Substances 0.000 claims description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 7
- 235000011187 glycerol Nutrition 0.000 claims description 6
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 238000001125 extrusion Methods 0.000 claims description 3
- 125000005429 oxyalkyl group Chemical group 0.000 claims description 3
- 229920000223 polyglycerol Polymers 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims 3
- 230000000694 effects Effects 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 10
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 238000002156 mixing Methods 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 4
- 239000005022 packaging material Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 4
- OBKHWBKDEYYYOY-UHFFFAOYSA-N 2-octadecylperoxyethanamine Chemical compound C(CCCCCCCCCCCCCCCCC)OOCCN OBKHWBKDEYYYOY-UHFFFAOYSA-N 0.000 description 3
- 239000002216 antistatic agent Substances 0.000 description 3
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- CNFSKVVUWAGXIT-UHFFFAOYSA-N CC(CCCCCCCCCCCCCCCC)OOCCN Chemical compound CC(CCCCCCCCCCCCCCCC)OOCCN CNFSKVVUWAGXIT-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 229960000541 cetyl alcohol Drugs 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- IRHTZOCLLONTOC-UHFFFAOYSA-N hexacosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCO IRHTZOCLLONTOC-UHFFFAOYSA-N 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229940043348 myristyl alcohol Drugs 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 235000003441 saturated fatty acids Nutrition 0.000 description 2
- 229940012831 stearyl alcohol Drugs 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 229920003067 (meth)acrylic acid ester copolymer Polymers 0.000 description 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- PHDVPEOLXYBNJY-KTKRTIGZSA-N 2-(2-hydroxyethoxy)ethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCOCCO PHDVPEOLXYBNJY-KTKRTIGZSA-N 0.000 description 1
- LZSVYIQKUAVZFB-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCCOCCO LZSVYIQKUAVZFB-UHFFFAOYSA-N 0.000 description 1
- WXINGHLXFZRQGX-UHFFFAOYSA-N 2-dodecylperoxyethanamine Chemical compound CCCCCCCCCCCCOOCCN WXINGHLXFZRQGX-UHFFFAOYSA-N 0.000 description 1
- TVIMZSOUQXNWHO-UHFFFAOYSA-N 2-tetradecanoylglycerol Chemical compound CCCCCCCCCCCCCC(=O)OC(CO)CO TVIMZSOUQXNWHO-UHFFFAOYSA-N 0.000 description 1
- DUUKZBGYNMHUHO-UHFFFAOYSA-N 253MC0P0YV Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)COCC(O)CO DUUKZBGYNMHUHO-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- CGBXSWXZXBQCMR-UHFFFAOYSA-N Glycerol 1-hexadecanoate Chemical compound OCC(O)CO.CCCCCCCCCCCCCCCC(O)=O CGBXSWXZXBQCMR-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000269851 Sarda sarda Species 0.000 description 1
- OGELJRHPEZALCC-UHFFFAOYSA-N [3-(2,3-dihydroxypropoxy)-2-hydroxypropyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(O)COCC(O)CO OGELJRHPEZALCC-UHFFFAOYSA-N 0.000 description 1
- WOGWRXSITPCETK-UHFFFAOYSA-N [3-(2,3-dihydroxypropoxy)-2-hydroxypropyl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)COCC(O)CO WOGWRXSITPCETK-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- UWLPCYBIJSLGQO-UHFFFAOYSA-N dodecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCC(O)=O UWLPCYBIJSLGQO-UHFFFAOYSA-N 0.000 description 1
- 238000009820 dry lamination Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- WECGLUPZRHILCT-HZJYTTRNSA-N rac-1-monolinoleoylglycerol Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(O)CO WECGLUPZRHILCT-HZJYTTRNSA-N 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
Landscapes
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はポリオレフィン樹脂フィルムに関するものであ
る。詳しくは、本発明は帯電防止効果の持続性に優れた
ポリオレフィン樹脂フィルムに関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a polyolefin resin film. Specifically, the present invention relates to a polyolefin resin film with excellent long-lasting antistatic effect.
ポリオレフィン樹脂フィルムは電気絶縁性に優れている
が、この反面静電気を帯びやすく、このためフィルム表
面に粉体やほこりが付着しやすくフィルム成形時の作業
性及びフィルムの商品価値が低下する。これらの欠点を
改善するために予め帯電防止剤をポリオレフィン樹脂に
添加し、混練した後フィルムを成形する方法が採用され
ている。Polyolefin resin films have excellent electrical insulation properties, but on the other hand, they tend to be charged with static electricity, and therefore powder and dust tend to adhere to the film surface, reducing workability during film molding and reducing the film's commercial value. In order to improve these drawbacks, a method has been adopted in which an antistatic agent is added to the polyolefin resin in advance, the resin is kneaded, and then a film is formed.
しかしながら、薬包材、コーヒ粉袋、かつお筒袋等の粉
末包装用包材には、帯電防止剤を含有するポリオレフィ
ン樹脂フィルムが使用されているが、長期間、例えば3
ケ月以上にわたり帯電防止効果を持続させることができ
ず、この持続性の改善が要望されている。However, polyolefin resin films containing antistatic agents are used for powder packaging materials such as medicine packaging materials, coffee powder bags, bonito tube bags, etc.
The antistatic effect cannot be sustained for more than several months, and there is a demand for improvement in this sustainability.
本発明者等は上記したポリオレフィン樹脂フィルムの帯
電防止性の長期間にわたり持続させるべく鋭意検討した
結果、特定の帯電防止剤と高級アルコールを併用してポ
リオレフィン樹脂フィルムに特定量配合することにより
、該フィルムの帯電防止性が著しく延長できることを見
出し、本発明を完成した。The inventors of the present invention have made extensive studies to maintain the antistatic properties of the polyolefin resin film described above over a long period of time. The present invention was completed based on the discovery that the antistatic properties of the film can be significantly extended.
すなわち、本発明の要旨はポリオレフィン樹脂を押出成
形して得られたフィルムであって、フィルム中に下記a
〜dの添加剤がフィルム厚み(μm)とフィルム中のa
−dの添加剤の合計濃度(重6%(以下wt%と略す
))との積が4〜10(μm、wt%)の範囲で配合さ
れており、その量比がa / b / c / d =
1 / 0.05〜1 / 0.04〜0.8 /
0〜1の割合であることを特徴とするポリオレフィン樹
脂フィルム。That is, the gist of the present invention is a film obtained by extrusion molding a polyolefin resin, which contains the following a.
The additives from ~d to the film thickness (μm) and a in the film
The product of -d and the total concentration of additives (6% by weight (hereinafter abbreviated as wt%)) is blended in a range of 4 to 10 (μm, wt%), and the quantitative ratio is a / b / c / d =
1/0.05~1/0.04~0.8/
A polyolefin resin film characterized in that the ratio is 0 to 1.
a 一般式(I)で示されるポリグリセリン脂肪酸エス
テル
CH20COR。a Polyglycerol fatty acid ester CH20COR represented by general formula (I).
CHOH
H2
CHOH
CR20H
(式中、R1は炭素数11〜21のアルキル又はアルケ
ニル基を示す。)
b 一般式(II)で示されるポリオキシアルキレンア
ルキルアミン
(式中、R2は炭素数8〜22の直鎖又は分岐鎖のアル
キル基、オキシアルキル基、アルケニル基又はオキジア
ルケニル基を示し、R3及びR4は炭素数2または3の
アルキレン基を示し、mとnはm + n = 2〜1
0の整数を表わす。)C高級脂肪族アルコール
d 一般式(III)で示される高級脂肪酸グリセリン
エステル
CHzOCORs
CHOH・・・・・・(III)
H20H
(式中、R3は炭素数11〜21のアルキル基又はアル
ケニル基を示す。)
に存する。CHOH H2 CHOH CR20H (In the formula, R1 represents an alkyl or alkenyl group having 11 to 21 carbon atoms.) b Polyoxyalkylenealkylamine represented by the general formula (II) (In the formula, R2 represents an alkyl or alkenyl group having 8 to 22 carbon atoms. Represents a linear or branched alkyl group, oxyalkyl group, alkenyl group or oxydialkenyl group, R3 and R4 represent an alkylene group having 2 or 3 carbon atoms, m and n are m + n = 2 to 1
Represents an integer of 0. ) C higher aliphatic alcohol d Higher fatty acid glycerin ester represented by general formula (III) CHzOCORs CHOH... (III) H20H (wherein, R3 represents an alkyl group or alkenyl group having 11 to 21 carbon atoms ).
本発明におけるポリオレフィン樹脂としてはエチレンま
たはプロピレンの単独重合体及びエチレン主体の共重合
体、例えば、高圧法低密度ポリエチレン、線状低密度ポ
リエチレン、中密度ポリエチレン、高密度ポリエチレン
、ポリプロピレン、エチレン−プロピレン共重合体、エ
チレン−ブテン−1共重合体、エチレン−酢酸ビニル共
重合体、エチレン−(メタ)アクリル酸共重合体、エチ
レン−(メタ)アクリル酸エステル共重合体等が挙げら
れる。また、これらのポリオレフィン樹脂を不飽和カル
ボン酸またはその無水物、例えば無水マレイン酸等でグ
ラフト反応させて変性させたものであってもよい。The polyolefin resins used in the present invention include ethylene or propylene homopolymers and ethylene-based copolymers, such as high-pressure low-density polyethylene, linear low-density polyethylene, medium-density polyethylene, high-density polyethylene, polypropylene, and ethylene-propylene. Polymers, ethylene-butene-1 copolymer, ethylene-vinyl acetate copolymer, ethylene-(meth)acrylic acid copolymer, ethylene-(meth)acrylic acid ester copolymer, and the like. Furthermore, these polyolefin resins may be modified by graft reaction with an unsaturated carboxylic acid or its anhydride, such as maleic anhydride.
上記ポリオレフィン樹脂の物性としてはフィルム成形用
のものであれば特に制限されるものではない。The physical properties of the polyolefin resin are not particularly limited as long as it is used for film forming.
本発明に用いられる樹脂組成物としては上記ポリオレフ
ィン樹脂にポリグリセリン脂肪酸エステルとポリオキシ
アルキレンアルキルアミンならびに高級脂肪酸グリセリ
ンエステルの帯電防止剤を併用し、且つ、これに高級脂
肪族アルコールを配合したものが使用される。The resin composition used in the present invention is one in which the polyolefin resin is combined with an antistatic agent of polyglycerin fatty acid ester, polyoxyalkylene alkylamine, and higher fatty acid glycerin ester, and a higher aliphatic alcohol is blended therein. used.
ポリグリセリン脂肪酸エステル(以下a成分という)と
しては下記一般式(I)で示される化合物が使用される
。As the polyglycerol fatty acid ester (hereinafter referred to as component a), a compound represented by the following general formula (I) is used.
CHz OCOR+ HOH CH。Chz OCOR+ HOH CH.
HOH
H20H
(式中、R+ は炭素数11〜21のアルキル又はアル
ケニル基を示す。)
上記化合物としてはポリグリセリンと炭素数12〜22
の飽和又は不飽和の脂肪酸のモノエステル化合物、例え
ば、ジグリセリンモノラウレート、ジグリセリンモノミ
リステート、ジグリセリンモノパルミテート、ジグリセ
リンモノステアレート、ジグリセリンモノオレエート、
ジグリセリンモノリノーレート等が挙げられる。これら
の化合物は単独又は混合物のいずれも使用可能である。HOH H20H (In the formula, R+ represents an alkyl or alkenyl group having 11 to 21 carbon atoms.) The above compounds include polyglycerin and 12 to 22 carbon atoms.
monoester compounds of saturated or unsaturated fatty acids, such as diglycerol monolaurate, diglycerol monomyristate, diglycerol monopalmitate, diglycerol monostearate, diglycerol monooleate,
Examples include diglycerol monolinoleate. These compounds can be used alone or in mixtures.
ポリオキシアルキレンアルキルアミン(以下す成分とい
う)としては下記一般式(II)で示される化合物が使
用される。As the polyoxyalkylenealkylamine (hereinafter referred to as component), a compound represented by the following general formula (II) is used.
(式中、R2は炭素数8〜22の直鎖又は分岐鎖のアル
キル基、オキシアルキル基、アルケニル基又はオキジア
ルケニル基を示し、R3及びR4は炭素数2または3の
アルキレン基を示し、mとnはm + n = 2〜1
0の整数を表わす。)一般式(n)で表わされる化合物
としては、例えばドデシルジオキシエチルアミン、テI
・ラブシルジオキシエチルアミン、オクタデシルジオキ
シエチルアミン、16−オキシヘプタデシルジオキシエ
チルアミン、オクタデシルオキシオキシエトキシエチル
アミン、17−オクタデシルジオキシエチルアミン、1
−メチルヘプタデシルジオキシエチルアミン等が挙げら
れる。これらの化合物は単独又は混合物いずれも使用可
能である。(In the formula, R2 represents a linear or branched alkyl group, oxyalkyl group, alkenyl group, or oxydialkenyl group having 8 to 22 carbon atoms, and R3 and R4 represent an alkylene group having 2 or 3 carbon atoms, m and n are m + n = 2~1
Represents an integer of 0. ) Examples of the compound represented by the general formula (n) include dodecyldioxyethylamine, TeI
・Labsyldioxyethylamine, octadecyldioxyethylamine, 16-oxyheptadecyldioxyethylamine, octadecyloxyoxyethoxyethylamine, 17-octadecyldioxyethylamine, 1
-Methylheptadecyldioxyethylamine and the like. These compounds can be used alone or as a mixture.
さらに高級脂肪族アルコール(以下C成分という)とし
ては、炭素数12〜30のアルコールが好適に用いられ
る。該高級脂肪族アルコールとしては、例えば、ラウリ
ルアルコール、ミリスチルアルコール、セチルアルコー
ル、ステアリルアルコール、アルキルアルコール、ベヘ
ニルアルコール、セリルアルコール、コリャニルアルコ
ール等が挙げられ、特にステアリルアルコール、セチル
アルコール、ミリスチルアルコール、ラウリルアルコー
ル等の炭素数12〜20のアルコールが好適に用いられ
る。Further, as the higher aliphatic alcohol (hereinafter referred to as component C), an alcohol having 12 to 30 carbon atoms is preferably used. Examples of the higher aliphatic alcohol include lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, alkyl alcohol, behenyl alcohol, ceryl alcohol, coryanyl alcohol, and in particular stearyl alcohol, cetyl alcohol, myristyl alcohol, and lauryl alcohol. Alcohols having 12 to 20 carbon atoms are preferably used.
本発明におけるポリオレフィン樹脂フィルムにおいて、
上記3成分の添加剤に、さらに下記一般式(III)で
示される高級脂肪酸グリセリンエステルを添加して併用
することにより、フィルムの初期から長期にわたる帯電
防止効果がさらに改善されるので望ましい。In the polyolefin resin film of the present invention,
It is desirable to add and use higher fatty acid glycerin ester represented by the following general formula (III) in combination with the three additives described above, as this further improves the antistatic effect of the film from the initial stage to the long term.
上記高級脂肪酸グリセリンエステル(以下d成分という
)としては一般式(I)
CHzOCORs
CHOH・・・・・・ (I[[)
H2OH
(式中、R6は炭素数11〜21のアルキル基又はアル
ケニル基である。)
で表わされる化合物が用いられる。該化合物としては、
グリセリンと炭素数12〜22までの飽和又は不飽和の
脂肪酸のモノエステル化合物、例えばグリセリンモノラ
ウレート、グリセリンモノミリステート、グリセリンモ
ノパルミテート、グリセリンモノステアレート、グリセ
リンモノオレエート、グリセリンモノリノーレート等が
挙げられる。これらの化合物は単独又は混合物いずれも
使用可能である。The above-mentioned higher fatty acid glycerin ester (hereinafter referred to as component d) has the general formula (I) CHzOCORs CHOH... (I[[) H2OH (wherein, R6 is an alkyl group or alkenyl group having 11 to 21 carbon atoms) ) is used. As the compound,
Monoester compounds of glycerin and saturated or unsaturated fatty acids having 12 to 22 carbon atoms, such as glycerin monolaurate, glycerin monomyristate, glycerin monopalmitate, glycerin monostearate, glycerin monooleate, glycerin monolinoleate, etc. can be mentioned. These compounds can be used alone or as a mixture.
本発明に用いられる樹脂組成物は上記各成分を予備混合
した後、混練する方法、上記各成分を一度に混合、混練
する方法等により得ることができる。該混合、混練は例
えば、リボンブレンダータンブルミキサー、ヘンシェル
ミキサー等により、また、該混練はオープンロール、パ
ンバリミキサ、車軸スクリュー押出機、二輪スクリュー
押出機、混練機等により行なうことができる。The resin composition used in the present invention can be obtained by a method in which the above components are premixed and then kneaded, or by a method in which the above components are mixed and kneaded all at once. The mixing and kneading can be carried out using, for example, a ribbon blender, tumble mixer, Henschel mixer, etc., and the kneading can be carried out using an open roll, a panburi mixer, an axle screw extruder, a two-wheel screw extruder, a kneader, etc.
このようにして得られるポリオレフィン樹脂組成物はイ
ンフレーション法又はTダイ法等の押出成形により、例
えば、140〜250℃の温度で溶融押出してフィルム
化される。フィルム厚みとしては、通常10〜200μ
mの範囲である。The polyolefin resin composition thus obtained is melt-extruded into a film by extrusion molding such as an inflation method or a T-die method, for example, at a temperature of 140 to 250°C. The film thickness is usually 10-200μ
m range.
本発明におけるポリオレフィン樹脂フィルム中の上記4
成分の配合量(合計)としてはフィルム厚さ(μm)と
フィルム中の上記4成分の合計濃度(wt%)の積が4
〜10(μm−wt%)、好ましくは6〜8 (μm
−w t%)の範囲であり、且つ、上記4成分の配合比
としてはa成分/b成分/C成分/d成分=110.0
5〜110.04〜0、8 / 0〜1、好ましくは1
10.05〜0.5 / 0゜04〜0.4 / 0〜
0.8の範囲である。上記4成分の配合量(合計)が下
限未満ではフィルムの帯電防止効果の持続性が低下し、
一方上限より多いと添加剤がフィルム表面に多量ブリー
ドし、ドライラミネート等を行なった際に、接着強度の
低下をきたすので好ましくない。4 above in the polyolefin resin film of the present invention
The amount (total) of the components is the product of the film thickness (μm) and the total concentration (wt%) of the above four components in the film, which is 4.
~10 (μm-wt%), preferably 6-8 (μm
-wt%), and the blending ratio of the above four components is component a/component b/component C/component d=110.0
5-110.04-0, 8/0-1, preferably 1
10.05~0.5/0°04~0.4/0~
It is in the range of 0.8. If the amount (total) of the above four components is less than the lower limit, the durability of the antistatic effect of the film will decrease,
On the other hand, if the amount exceeds the upper limit, a large amount of the additive will bleed onto the film surface, resulting in a decrease in adhesive strength when dry laminating or the like is performed, which is not preferable.
また、上記す成分の配合比が下限未満ではフィルムの帯
電防止効果及びその持続性が低下し、方、上限より多い
と添加剤がフィルム表面に多量ブリードし、ドライラミ
ネート等を行なった際に、接着強度の低下をきたすので
好ましくない。In addition, if the blending ratio of the above-mentioned components is less than the lower limit, the antistatic effect of the film and its sustainability will decrease, while if it is more than the upper limit, a large amount of the additive will bleed onto the film surface, and when dry laminating etc. are performed, This is not preferable because it causes a decrease in adhesive strength.
さらに、上記C成分の配合比が下限未満では帯電防止効
果の即効性がなく、初期の帯電防止効果が不十分であり
、一方、上限より多いと添加剤がフィルム表面に多量ブ
リードし、ドライラミネート等を行なった際に、接着強
度の低下をきたすので好ましくない。Furthermore, if the blending ratio of component C is less than the lower limit, the antistatic effect will not be immediate and the initial antistatic effect will be insufficient.On the other hand, if it is more than the upper limit, a large amount of the additive will bleed onto the film surface, resulting in dry lamination. This is not preferable because it causes a decrease in adhesive strength.
上記a成分は長期における帯電防止性を付与させる効果
を有し、上記す及びC成分と併用することにより、初期
から長期にわたり帯電防止効果をバランスよ(付与させ
ることができる。The above-mentioned component a has the effect of imparting long-term antistatic properties, and when used in combination with the above-mentioned components A and C, the antistatic effect can be balanced and imparted over a long period of time from the initial stage.
また、上記d成分は上記a ”−C成分に添加して併用
することにより、フィルムの初期から長期にわたり帯電
防止効果がさらに改良されるが、その配合比が上限より
多いと添加剤がフィルム表面に多量ブリードし、ドライ
ラミネート等を行なった際に、接着強度の低下をきたす
ので好ましくない。In addition, when the d component is added to the a''-C component and used in combination, the antistatic effect of the film can be further improved over a long period of time from the initial stage of the film.However, if the blending ratio is higher than the upper limit, the additive may be added to the film surface. This is not preferable because it bleeds in large quantities and reduces adhesive strength when dry laminating or the like is performed.
以下本発明を実施例により、更に詳述するが、本発明は
その要旨を超えない限りこれらの実施例により何ら限定
されるものではない。The present invention will be explained in more detail below with reference to examples, but the present invention is not limited to these examples in any way unless it exceeds the gist thereof.
なお、実施例中の物性の測定は以下のように行なった。The physical properties in the examples were measured as follows.
fl) 表面固有抵抗
超絶縁抵抗計(安藤電気製、VMG−1000型)を用
いて、フィルム表面の表面固有抵抗値を測定した。fl) Surface specific resistance The surface specific resistance value of the film surface was measured using a super insulation resistance meter (manufactured by Ando Electric, model VMG-1000).
(2)帯電圧の半減期
スタティソクオネストメーター(大月商会製)でフィル
ム表面に1QkVで1分間、1cmの距離で帯電させ、
帯電した電圧の減衰時間(半減期)を測定した。(2) Half-life of electrostatic voltage Statistic Charge the surface of the film at 1 QkV for 1 minute at a distance of 1 cm using a sonic honesty meter (manufactured by Otsuki Shokai).
The decay time (half-life) of the charged voltage was measured.
実施例1
高圧法低密度ポリエチレン(メルトインデソクス1.3
g/10分、密度0.924g/cIa)にオクタデシ
ルジオキシエチルアミン(b成分)0.02重量%、ジ
グリセリンモノステアレート(C成分)0、175重量
%及びステアリルアルコール(C成分)0.015重量
%を配合した樹脂を樹脂温度180℃で、ブローアツプ
比1.5、フロストライン高さ25備の条件でインフレ
ーション成形し、30μm厚のフィルムを得た。このも
のを23℃、65%の雰囲気下で保管し、成形3日後、
2.5月後、4月後に表面固有抵抗及び帯電圧半減期を
測定した。Example 1 High pressure process low density polyethylene (melt index 1.3
g/10 min, density 0.924 g/cIa), 0.02% by weight of octadecyldioxyethylamine (component B), 0.175% by weight of diglycerin monostearate (component C), and 0.0% by weight of stearyl alcohol (component C). A resin containing 015% by weight was inflation-molded at a resin temperature of 180° C., a blow-up ratio of 1.5, and a frost line height of 25 to obtain a film with a thickness of 30 μm. This product was stored in an atmosphere of 23°C and 65%, and after 3 days of molding,
After 2.5 months and after 4 months, surface resistivity and charging voltage half-life were measured.
結果を第1表に示す。The results are shown in Table 1.
実施例2
添加剤をジグリセリンモノステアレート(C成分)0.
10重量%、オクタデシルジオキシエチルアミン(b成
分)0.02重量%、ステアリルアルコール(C成分)
0.15重量%及びグリセリンモノステアレート(d成
分)0.075重量%とじた他は実施例1と同様に行な
った。Example 2 Diglycerol monostearate (component C) 0.
10% by weight, octadecyldioxyethylamine (component B) 0.02% by weight, stearyl alcohol (component C)
The same procedure as in Example 1 was conducted except that 0.15% by weight and 0.075% by weight of glycerin monostearate (component d) were added.
結果を第1表に示す。The results are shown in Table 1.
比較例1〜4
添加剤の配合量を第1表のように変えたこと以外は、実
施例1,2と同様に行なった。Comparative Examples 1 to 4 Comparative Examples 1 to 4 were conducted in the same manner as Examples 1 and 2, except that the amounts of additives were changed as shown in Table 1.
結果を第1表に示す。The results are shown in Table 1.
本発明により帯電防止効果が4ケ月以上持続するポリオ
レフィン樹脂フィルムが得られ、薬包材、粉末包装用包
材に利用できる。According to the present invention, a polyolefin resin film whose antistatic effect lasts for 4 months or more can be obtained, and can be used for medicine packaging materials and powder packaging materials.
Claims (1)
ルムであって、フィルム中に下記a〜dの添加剤がフィ
ルム厚み(μm)とフィルム中のa〜dの添加剤の合計
濃度(重量%(wt%と略す))との積が4〜10(μ
m.wt%)の範囲で配合されており、その重量比がa
/b/c/d=1/0.05〜1/0.04〜0.8/
0〜1の割合であることを特徴とするポリオレフィン樹
脂フィルム。 a 一般式( I )で示されるポリグリセリン脂肪酸エ
ステル ▲数式、化学式、表等があります▼……( I ) (式中、R_1は炭素数11〜21のアルキル又はアル
ケニル基を示す。) b 一般式(II)で示されるポリオキシアルキレンアル
キルアミン ▲数式、化学式、表等があります▼……(II) (式中、R_2は炭素数8〜22の直鎖又は分岐鎖のア
ルキル基、オキシアルキル基、アルケニル基又はオキシ
アルケニル基を示し、R_3及びR_4は炭素数2また
は3のアルキレン基を示し、mとnはm+n=2〜10
の整数を表わす。) c 高級脂肪族アルコール d 一般式(III)で示される高級脂肪酸グリセリンエ
ステル ▲数式、化学式、表等があります▼……(III) (式中、R_5は炭素数11〜21のアルキル基又はア
ルケニル基を示す。)(1) A film obtained by extrusion molding a polyolefin resin, in which the following additives a to d are added to the film thickness (μm) and the total concentration (wt%) of the additives a to d in the film. (abbreviated as wt%)) is 4 to 10 (μ
m. wt%), and the weight ratio is a
/b/c/d=1/0.05~1/0.04~0.8/
A polyolefin resin film characterized in that the ratio is 0 to 1. a Polyglycerol fatty acid ester represented by the general formula (I) ▲ Numerical formula, chemical formula, table, etc. are available ▼... (I) (In the formula, R_1 represents an alkyl or alkenyl group having 11 to 21 carbon atoms.) b General Polyoxyalkylenealkylamine represented by formula (II) ▲ Numerical formulas, chemical formulas, tables, etc. are available ▼... (II) (In the formula, R_2 is a straight or branched alkyl group having 8 to 22 carbon atoms, oxyalkyl group, alkenyl group or oxyalkenyl group, R_3 and R_4 represent an alkylene group having 2 or 3 carbon atoms, m and n are m+n=2 to 10
represents an integer. ) c Higher aliphatic alcohol d Higher fatty acid glycerin ester represented by the general formula (III) ▲ Numerical formulas, chemical formulas, tables, etc. are available ▼ ... (III) (In the formula, R_5 is an alkyl group or alkenyl having 11 to 21 carbon atoms (indicates the group)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP801090A JP2849425B2 (en) | 1990-01-17 | 1990-01-17 | Polyolefin resin film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP801090A JP2849425B2 (en) | 1990-01-17 | 1990-01-17 | Polyolefin resin film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03212435A true JPH03212435A (en) | 1991-09-18 |
| JP2849425B2 JP2849425B2 (en) | 1999-01-20 |
Family
ID=11681382
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP801090A Expired - Fee Related JP2849425B2 (en) | 1990-01-17 | 1990-01-17 | Polyolefin resin film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2849425B2 (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05169601A (en) * | 1991-12-24 | 1993-07-09 | Mitsubishi Kasei Corp | Laminate for packaging powder |
| JP2008184478A (en) * | 2007-01-26 | 2008-08-14 | Riken Vitamin Co Ltd | Antistatic polypropylene film |
| JP2008303272A (en) * | 2007-06-06 | 2008-12-18 | Kao Corp | Polyolefin resin composition |
| EP2477619A4 (en) * | 2009-09-17 | 2013-07-03 | B Eugene Guthery | Nasal, wound and skin formulations and methods for control of antibiotic-resistant staphylococci and other gram-positive bacteria |
| WO2018216305A1 (en) | 2017-05-22 | 2018-11-29 | 竹本油脂株式会社 | Polyolefin resin modifier, polyolefin resin composition, modified polyolefin resin film, and laminated film |
| WO2020070846A1 (en) | 2018-10-04 | 2020-04-09 | 竹本油脂株式会社 | Modifier for polyolefin resin |
-
1990
- 1990-01-17 JP JP801090A patent/JP2849425B2/en not_active Expired - Fee Related
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05169601A (en) * | 1991-12-24 | 1993-07-09 | Mitsubishi Kasei Corp | Laminate for packaging powder |
| JP2008184478A (en) * | 2007-01-26 | 2008-08-14 | Riken Vitamin Co Ltd | Antistatic polypropylene film |
| JP2008303272A (en) * | 2007-06-06 | 2008-12-18 | Kao Corp | Polyolefin resin composition |
| EP2477619A4 (en) * | 2009-09-17 | 2013-07-03 | B Eugene Guthery | Nasal, wound and skin formulations and methods for control of antibiotic-resistant staphylococci and other gram-positive bacteria |
| WO2018216305A1 (en) | 2017-05-22 | 2018-11-29 | 竹本油脂株式会社 | Polyolefin resin modifier, polyolefin resin composition, modified polyolefin resin film, and laminated film |
| WO2020070846A1 (en) | 2018-10-04 | 2020-04-09 | 竹本油脂株式会社 | Modifier for polyolefin resin |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2849425B2 (en) | 1999-01-20 |
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