JPH04214343A - Laminate for cartridge agent material - Google Patents
Laminate for cartridge agent materialInfo
- Publication number
- JPH04214343A JPH04214343A JP40139690A JP40139690A JPH04214343A JP H04214343 A JPH04214343 A JP H04214343A JP 40139690 A JP40139690 A JP 40139690A JP 40139690 A JP40139690 A JP 40139690A JP H04214343 A JPH04214343 A JP H04214343A
- Authority
- JP
- Japan
- Prior art keywords
- density polyethylene
- low density
- laminate
- polyethylene
- layer
- 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
- 239000000463 material Substances 0.000 title claims abstract description 22
- 229920001684 low density polyethylene Polymers 0.000 claims abstract description 30
- 239000004702 low-density polyethylene Substances 0.000 claims abstract description 30
- 238000001125 extrusion Methods 0.000 claims abstract description 16
- 239000011342 resin composition Substances 0.000 claims abstract description 11
- 229920013716 polyethylene resin Polymers 0.000 claims abstract description 9
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims abstract description 8
- 150000003973 alkyl amines Chemical class 0.000 claims abstract description 5
- 230000000704 physical effect Effects 0.000 claims abstract description 5
- 150000002148 esters Chemical class 0.000 claims abstract 2
- 239000005022 packaging material Substances 0.000 claims description 16
- 239000003814 drug Substances 0.000 claims description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 235000011187 glycerol Nutrition 0.000 claims description 7
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000005429 oxyalkyl group Chemical group 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims 1
- -1 polyethylene Polymers 0.000 abstract description 16
- 238000010030 laminating Methods 0.000 abstract description 5
- 239000000203 mixture Substances 0.000 abstract description 5
- 239000004698 Polyethylene Substances 0.000 abstract description 4
- 229920000573 polyethylene Polymers 0.000 abstract description 4
- 239000002994 raw material Substances 0.000 abstract description 2
- 239000002253 acid Substances 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 description 15
- 230000001070 adhesive effect Effects 0.000 description 15
- 239000010410 layer Substances 0.000 description 15
- 239000010408 film Substances 0.000 description 13
- 229920005989 resin Polymers 0.000 description 12
- 239000011347 resin Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 11
- 238000000034 method Methods 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 238000003475 lamination Methods 0.000 description 7
- 239000000654 additive Substances 0.000 description 6
- 239000002216 antistatic agent Substances 0.000 description 6
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
- 239000000155 melt Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 229940043276 diisopropanolamine Drugs 0.000 description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 229920005672 polyolefin resin Polymers 0.000 description 4
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 4
- 239000010409 thin film Substances 0.000 description 4
- 229920000298 Cellophane Polymers 0.000 description 3
- 239000012790 adhesive layer Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 238000009512 pharmaceutical packaging Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- NDLNTMNRNCENRZ-UHFFFAOYSA-N 2-[2-hydroxyethyl(octadecyl)amino]ethanol Chemical compound CCCCCCCCCCCCCCCCCCN(CCO)CCO NDLNTMNRNCENRZ-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229960000541 cetyl alcohol Drugs 0.000 description 2
- 238000000576 coating method Methods 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
- IRHTZOCLLONTOC-UHFFFAOYSA-N hexacosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCO IRHTZOCLLONTOC-UHFFFAOYSA-N 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229940043348 myristyl alcohol Drugs 0.000 description 2
- 229940012831 stearyl alcohol Drugs 0.000 description 2
- MUTYMGNMGRUBKV-QXMHVHEDSA-N (z)-n,n-bis(2-hydroxypropyl)octadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(CC(C)O)CC(C)O MUTYMGNMGRUBKV-QXMHVHEDSA-N 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
- CPHJEACXPATRSU-UHFFFAOYSA-N 2-[2-hydroxyethyl(tetradecyl)amino]ethanol Chemical compound CCCCCCCCCCCCCCN(CCO)CCO CPHJEACXPATRSU-UHFFFAOYSA-N 0.000 description 1
- NKFNBVMJTSYZDV-UHFFFAOYSA-N 2-[dodecyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCCCCCCCCCN(CCO)CCO NKFNBVMJTSYZDV-UHFFFAOYSA-N 0.000 description 1
- MJWIPTSHMLSLFE-UHFFFAOYSA-N 2-[hexadecyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCCCCCCCCCCCCCN(CCO)CCO MJWIPTSHMLSLFE-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
- CGBXSWXZXBQCMR-UHFFFAOYSA-N Glycerol 1-hexadecanoate Chemical compound OCC(O)CO.CCCCCCCCCCCCCCCC(O)=O CGBXSWXZXBQCMR-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 241000269851 Sarda sarda Species 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
- 238000003851 corona treatment Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 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
- 229940079593 drug Drugs 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
- 239000011888 foil Substances 0.000 description 1
- 239000011086 glassine Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000005001 laminate film Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 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
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は薬包材用積層体に関する
ものである。詳しくは、本発明は帯電防止性能及びその
持続性共に優れたポリエチレン樹脂を用いた薬包材用積
層体に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a laminate for medicine packaging materials. Specifically, the present invention relates to a laminate for medicine packaging materials using a polyethylene resin that has excellent antistatic performance and durability.
【0002】0002
【従来の技術】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。[Prior Art] Polyolefin resin films have excellent electrical insulation properties, but on the other hand, they tend to be charged with static electricity, which makes it easy for powder and dust to adhere to the film surface, reducing workability during film molding and the commercial value of the film. descend. 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.
【0003】薬包材、コーヒー粉袋、かつお節袋等の粉
末包装用包材には、帯電防止剤を含有するポリオレフィ
ン樹脂フィルムを基材に高温下で押出ラミネートしたも
のが用いられるが、押出ラミネート時にフィルム中の帯
電防止剤が熱分解又は飛散してしまい、十分な帯電防止
効果が得られなかったり、短時間で帯電防止効果が著し
く低下してしまったり、基材との接着強度が低下する等
の問題点があった。[0003] Packaging materials for powder packaging, such as medicine packaging materials, coffee powder bags, and bonito flakes bags, are made by extrusion laminating a polyolefin resin film containing an antistatic agent as a base material at high temperatures. Sometimes, the antistatic agent in the film decomposes or scatters due to thermal decomposition, resulting in insufficient antistatic effect, or a significant decrease in antistatic effect in a short period of time, or a decrease in adhesive strength with the base material. There were problems such as.
【0004】これらの問題点を解決する方法として、本
出願人は先に、特定の帯電防止剤及び高級アルコールを
ポリオレフィン樹脂に特定量配合することにより、高温
下での押出ラミネート成形後においても一定の帯電防止
効果を有し、且つ長時間帯電防止効果が持続し、基材と
の接着強度の充分なラミネートフィルムが得られること
を見出し、特開平1−141932号に提案した。As a method to solve these problems, the present applicant has first formulated a specific amount of a specific antistatic agent and a higher alcohol into a polyolefin resin, thereby maintaining a constant level even after extrusion lamination molding at high temperatures. It has been found that a laminate film can be obtained which has an antistatic effect, maintains the antistatic effect for a long time, and has sufficient adhesive strength to the base material, and proposed it in JP-A-1-141932.
【0005】[0005]
【発明が解決しようとする課題】しかしながら、上記提
案方法では一定の帯電防止性能が望まれる用途には適用
できるが、高い帯電防止性能が要望される用途、例えば
、帯電しやすい又は帯電している粉末状又は顆粒状の薬
を包装するのに用いられる薬包材の用途には不適である
。[Problem to be Solved by the Invention] However, although the above proposed method can be applied to applications where a certain level of antistatic performance is desired, it cannot be applied to applications where high antistatic performance is desired, such as those that easily charge or are charged. It is unsuitable for use as medicine packaging materials used to package powdered or granular medicines.
【0006】[0006]
【課題を解決するための手段】本発明者等は上記した高
い帯電防止性能が要望される薬包材の用途に適する包装
材につき鋭意検討を重ねた結果、基材上に低密度ポリエ
チレン層及び特定の帯電防止剤及び高級アルコールを低
密度ポリエチレンに特定量配合した樹脂組成物層を順次
押出ラミネートすることにより、高い帯電防止効果及び
その持続性に優れた積層体(薬包材用積層体)が得られ
ることを見出し、本発明を完成した。[Means for Solving the Problems] The present inventors have conducted intensive studies on packaging materials suitable for the use of drug packaging materials that require high antistatic performance as described above, and have developed a packaging material with a low-density polyethylene layer on the base material. By sequentially extruding and laminating resin composition layers containing specific amounts of a specific antistatic agent and higher alcohol in low-density polyethylene, a laminate with high antistatic effect and excellent durability (laminate for drug packaging materials) The present invention was completed based on the discovery that the following can be obtained.
【0007】すなわち、本発明の要旨は基材の少なくと
も片面に密度が0.925g/cm3 以下の低密度ポ
リエチレン層並びに密度が0.925g/cm3 以下
の低密度ポリエチレンに下記一般式(I)で示されるポ
リオキシアルキレンアルキルアミン0.12〜0.3重
量%、高級脂肪酸グリセリンエステル0.25〜0.4
重量%及び高級脂肪族アルコール0.12〜0.2重量
%を配合してなるポリエチレン樹脂組成物層を順次押出
ラミネートしたものであって、その表面固有抵抗が5×
1010Ω以下の物性を有してなることを特徴とする薬
包材用積層体、に存する。That is, the gist of the present invention is to provide a low-density polyethylene layer having a density of 0.925 g/cm 3 or less on at least one side of the base material, and a low-density polyethylene layer having a density of 0.925 g/cm 3 or less represented by the following general formula (I). 0.12-0.3% by weight of the indicated polyoxyalkylene alkylamine, 0.25-0.4% of higher fatty acid glycerin ester
% by weight and higher aliphatic alcohol by 0.12 to 0.2% by weight are sequentially extruded and laminated, and the surface resistivity is 5×.
A laminate for medicine packaging material characterized by having physical properties of 1010Ω or less.
【0008】[0008]
【化2】[Case 2]
【0009】(式中、R1 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、R2 及びR3 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)。(In the formula, R1 represents a linear or branched alkyl group, oxyalkyl group, alkenyl group, or oxyalkenyl group having 8 to 22 carbon atoms, and R2 and R3 represent an alkylene group having 2 or 3 carbon atoms. and m and n are m+
n represents an integer from 2 to 10).
【0010】以下、本発明の薬包材用積層体につき、さ
らに詳細に説明する。本発明において基材としては上質
紙、クラフト紙、グラシン紙等の紙類、セロハン、ナイ
ロン、ポリエチレンテレフタレート、アルミ箔等が使用
される。また、基材に積層する低密度ポリエチレン層及
びポリエチレン樹脂組成物層の原料の低密度ポリエチレ
ンとしては分岐状の低密度ポリエチレン、すなわち、高
圧法の低密度ポリエチレンが好適に用いられる。The laminate for medicine packaging materials of the present invention will be explained in more detail below. In the present invention, the base material used is paper such as high-quality paper, kraft paper, glassine paper, cellophane, nylon, polyethylene terephthalate, aluminum foil, etc. Further, as the low density polyethylene that is the raw material for the low density polyethylene layer and the polyethylene resin composition layer to be laminated on the base material, branched low density polyethylene, that is, high pressure low density polyethylene is preferably used.
【0011】該低密度ポリエチレンとしては密度が0.
925g/cm3以下、好ましくは0.910〜0.9
25g/cm3 、特に好ましくは0.915〜0.9
25g/cm3 の範囲であり、また{メルトインデッ
クスの値}×{溶融張力の値}で表わされる分子量分布
指数が10〜40の範囲、望ましくは10〜35の範囲
で、且つ、メルトインデックスが1〜50g/10分の
範囲、望ましくは2〜25g/10分の範囲のものが押
出ラミネート成形性の点から好適である。上記メルトイ
ンデックスはJIS K6760(ポリエチレン試験
方法)のメルトインデックスの測定法に準拠し、190
℃、2.16kgで測定した値であり、また、溶融張力
は樹脂をJIS K6760のメルトインデックスの
測定法において使用するノズルから160℃、0.25
g/分で押出し、1.52m/分の速度で引張ったとき
のノズルから25cm離れたところで測定した張力であ
る。[0011] The low density polyethylene has a density of 0.
925g/cm3 or less, preferably 0.910 to 0.9
25g/cm3, particularly preferably 0.915-0.9
25 g/cm3, the molecular weight distribution index expressed by {melt index value} x {melt tension value} is in the range of 10 to 40, preferably 10 to 35, and the melt index is in the range of 1 A range of 50 g/10 minutes, preferably 2 to 25 g/10 minutes is suitable from the viewpoint of extrusion lamination moldability. The above melt index is based on the melt index measurement method of JIS K6760 (polyethylene test method), and is 190
The value was measured at 160°C and 2.16 kg, and the melt tension was measured at 160°C and 0.25 kg from the nozzle used in the JIS K6760 melt index measurement method.
This is the tension measured at a distance of 25 cm from the nozzle when extruded at a speed of 1.52 m/min and pulled at a speed of 1.52 m/min.
【0012】上記低密度ポリエチレンの密度が上限より
高いと紙基材との接着性が低下し、また0.91g/c
m3 未満では成形性が低下する。また、メルトインデ
ックスが1g/10分未満では溶融膜の延展性が低下し
、一方50g/10分を超えると溶融時のネックインが
大きく、品質の良好な押出ラミネート物の製造が難しく
なる。また、上記した分子量分布指数が10未満ではネ
ックインが過大であり、且つドローレゾナンス現象を生
起してラミネート成形性が悪化し、また分子量分布指数
が40を超えた場合には、ラミネート成形品の表面の肌
荒れが大きくなるので望ましくない。[0012] If the density of the low-density polyethylene is higher than the upper limit, the adhesion to the paper base material will decrease, and the density of 0.91 g/c
If it is less than m3, moldability will decrease. Furthermore, if the melt index is less than 1 g/10 minutes, the spreadability of the molten film will decrease, while if it exceeds 50 g/10 minutes, the neck-in during melting will be large, making it difficult to produce a high-quality extruded laminate. Furthermore, if the above-mentioned molecular weight distribution index is less than 10, neck-in will be excessive and a draw resonance phenomenon will occur, resulting in poor laminate formability, and if the molecular weight distribution index exceeds 40, the laminate molded product will be This is undesirable as it increases the roughness of the surface.
【0013】本発明において、基材上に積層した低密度
ポリエチレン層上に押出ラミネートするポリエチレン樹
脂組成物層としては上記低密度ポリエチレンにポリオキ
シアルキレンアルキルアミンと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。In the present invention, the polyethylene resin composition layer to be extruded and laminated on the low-density polyethylene layer laminated on the base material is made by combining the low-density polyethylene with an antistatic agent of polyoxyalkylene alkylamine and higher fatty acid glycerin ester. In addition, a mixture containing a higher aliphatic alcohol is used.
【0014】ポリオキシアルキレンアルキルアミンとし
ては上記の一般式(I)で示される化合物が使用される
。一般式(I)で表わされる化合物としては、例えばラ
ウリルジエタノールアミン、ミリスチルジエタノールア
ミン、パルミチルジエタノールアミン、ステアリルジエ
タノールアミン、オレインジエタノールアミン、ラウリ
ルジイソプロパノールアミン、ミリスチルジイソプロパ
ノールアミン、パルミチルジイソプロパノールアミン、
ステアリルジイソプロパノールアミン、オレインジイソ
プロパノー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。As the polyoxyalkylenealkylamine, a compound represented by the above general formula (I) is used. Examples of the compound represented by the general formula (I) include lauryl diethanolamine, myristyl diethanolamine, palmityl diethanolamine, stearyl diethanolamine, oleic diethanolamine, lauryl diisopropanolamine, myristyl diisopropanolamine, palmityl diisopropanolamine,
Examples include stearyl diisopropanolamine and oleic diisopropanolamine. These compounds can be used alone or as a mixture.
【0015】また、高級脂肪酸グリセリンエステルとし
ては一般式(II)
(式中、R4 は炭素数11〜21までのアルキル基又
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12〜2
2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。Further, as the higher fatty acid glycerin ester, a compound represented by the general formula (II) (wherein R4 is an alkyl group or alkenyl group having 11 to 21 carbon atoms) is used. The compound includes glycerin and carbon atoms having 12 to 2 carbon atoms.
Monoester compounds of up to 2 saturated or unsaturated fatty acids, such as glycerin monolaurate, glycerin monomyristate, glycerin monopalmitate, glycerin monostearate, glycerin monooleate, glycerin monolinoleate, etc. These compounds can be used alone or as a mixture.
【0016】さらに高級脂肪族アルコールとしては、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、アラキルアルコール、ベヘニルアル
コール、セリルアルコール、コリヤ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, alcohols having 12 to 30 carbon atoms are preferably used. Examples of the higher aliphatic alcohol include lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, arachyl alcohol, behenyl alcohol, ceryl alcohol, coryanyl alcohol, etc. In particular, stearyl alcohol, cetyl alcohol, myristyl alcohol, lauryl alcohol, etc. Alcohols having 12 to 20 carbon atoms such as alcohol are preferably used.
【0017】上記ポリエチレン組成物は上記した低密度
ポリエチレンにポリオキシアルキレンアルキルアミン(
a)0.12〜0.3重量%、好ましくは0.12〜0
.25重量%、高級脂肪酸グリセリンエステル(b)0
.25〜0.4重量%、好ましくは0.25〜0.35
重量%及び高級脂肪族アルコール0.12〜0.25重
量%、好ましくは0.12〜0.2重量%を配合したも
のである。ポリオキシアルキレンアルキルアミンの配合
量が上記範囲未満では帯電防止効果及びその持続性が低
下し、上記範囲より多いと、押出ラミネートした場合添
加剤が樹脂と基材との接着層の界面に移行し、接着強度
の低下を引き起こすので好ましくない。また、高級脂肪
酸グリセリンエステルの配合量が、上記範囲未満では帯
電防止効果が小さく、上記範囲より多いと、添加剤が樹
脂表面にブリードして白化し、帯電防止効果が逆に低下
したり、押出ラミネートした場合添加剤が樹脂と基材と
の接着層の界面に移行し、接着強度の低下を引き起こす
ので好ましくない。さらに、高級脂肪族アルコールの配
合量が上記範囲未満では、帯電防止効果に即効性がなく
、上記範囲より多いと、押出ラミネートした場合添加剤
が樹脂と基材との接着層の界面に移行し、接着強度の低
下を引き起こすので好ましくない。The above-mentioned polyethylene composition comprises the above-mentioned low-density polyethylene and polyoxyalkylenealkylamine (
a) 0.12-0.3% by weight, preferably 0.12-0.
.. 25% by weight, higher fatty acid glycerin ester (b) 0
.. 25-0.4% by weight, preferably 0.25-0.35
% by weight and higher aliphatic alcohol by 0.12 to 0.25% by weight, preferably 0.12 to 0.2% by weight. If the amount of polyoxyalkylene alkylamine is less than the above range, the antistatic effect and its sustainability will decrease, and if it is more than the above range, the additive will migrate to the interface of the adhesive layer between the resin and the base material when extrusion lamination is performed. , which is not preferable because it causes a decrease in adhesive strength. In addition, if the amount of higher fatty acid glycerin ester blended is less than the above range, the antistatic effect will be small, and if it is more than the above range, the additive will bleed onto the resin surface and cause whitening, which may reduce the antistatic effect or cause extrusion. When laminated, the additive migrates to the interface of the adhesive layer between the resin and the base material, causing a decrease in adhesive strength, which is not preferable. Furthermore, if the amount of higher aliphatic alcohol is less than the above range, the antistatic effect will not be immediate, and if it is more than the above range, the additive will migrate to the interface of the adhesive layer between the resin and the base material when extrusion lamination is performed. , which is not preferable because it causes a decrease in adhesive strength.
【0018】上記の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、該混練はオーブンロール、
バンバリミキサー、単軸スクリュー押出機、二軸スクリ
ュー押出機、混練機等により行なうことができる。The above resin composition 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 may be performed using, for example, a ribbon blender, tumble mixer, Henschel mixer, etc., and the kneading may be performed using an oven roll,
This can be carried out using a Banbury mixer, a single screw extruder, a twin screw extruder, a kneader, or the like.
【0019】本発明において、上記基材にまず前記した
低密度ポリエチレン層を押出ラミネートするには基材に
直接押出ラミネートしてもよいが、基材と低密度ポリエ
チレン層との接着力を高めるため基材の接着面にコロナ
処理、フレーム処理、アンカーコート処理等の公知の表
面活性処理を施した後押出ラミネートするのが望ましい
。上記アンカーコート処理はポリウレタン系アルキルチ
タネート系、ポリエチレンイミン系、イソシアネート系
等の公知のアンカーコート剤を上記基材フィルムまたは
シートの表面に塗布することにより行なえば良い。In the present invention, in order to first extrusion-laminate the low-density polyethylene layer on the base material, extrusion lamination may be performed directly on the base material, but in order to increase the adhesive strength between the base material and the low-density polyethylene layer, It is desirable to perform extrusion lamination after subjecting the adhesive surface of the base material to a known surface activation treatment such as corona treatment, flame treatment, or anchor coating treatment. The anchor coating treatment may be carried out by applying a known anchor coating agent such as polyurethane-based alkyl titanate-based, polyethyleneimine-based, isocyanate-based, etc. to the surface of the base film or sheet.
【0020】上記押出ラミネート成形は公知の方法及び
装置を用いて行なうことができ、上記低密度ポリエチレ
ンを押出機のダイ(インフレーションダイ又はTダイ)
から樹脂温度300〜340℃で押出して溶融薄膜とな
し、該溶融薄膜を圧着ロールに導き、一方接着面に表面
活性処理を施すか又は未処理のまま同じく圧着ロールに
導びかれた上記基材フィルムまたはシートと圧着ラミネ
ートすることにより行なわれる。[0020] The above extrusion lamination molding can be carried out using a known method and apparatus.
A molten thin film is formed by extrusion from the resin at a resin temperature of 300 to 340°C, and the molten thin film is introduced into a pressure roll, while the adhesive surface is subjected to a surface activation treatment, or the above-mentioned base material is guided to the pressure roll without being treated. This is done by pressure laminating with a film or sheet.
【0021】次いで、基材の低密度ポリエチレン層上に
上記ポリエチレン樹脂組成物層を押出ラミネートする。
すなわち、該ポリエチレン樹脂組成物を押出機のダイ(
インフレーションダイ又はTダイ)から樹脂温度280
〜300℃で押出して溶融薄膜となし、該溶融薄膜を圧
着ロールに導き、同じ圧着ロールに導びかれた基材の低
密度ポリエチレン層と圧着ラミネートすることにより行
なわれる。[0021] Next, the above polyethylene resin composition layer is extrusion laminated onto the low density polyethylene layer of the base material. That is, the polyethylene resin composition is passed through the extruder die (
Inflation die or T die) to resin temperature 280
This is carried out by extruding at ~300° C. to form a molten thin film, leading the molten thin film to a pressure roll, and pressure laminating it with a low-density polyethylene layer of a base material guided by the same pressure roll.
【0022】上記基材に押出ラミネートする低密度ポリ
エチレン層及びポリエチレン樹脂組成物層の膜厚として
はそれぞれ10〜30μmの範囲である。上記方法で得
られた薬包材用積層体の表面固有抵抗は5×1010Ω
以下、好ましくは2×1010Ω以下、さらに好ましく
は1×1010Ω以下の物性値を有するものである。[0022] The thickness of the low density polyethylene layer and the polyethylene resin composition layer to be extrusion laminated on the above substrate is in the range of 10 to 30 μm, respectively. The surface resistivity of the laminate for medicine packaging material obtained by the above method is 5×1010Ω
Hereinafter, it preferably has a physical property value of 2×10 10 Ω or less, more preferably 1×10 10 Ω or less.
【0023】[0023]
【実施例】以下、本発明を実施例に基づいて更に詳細に
説明するが、本発明はその要旨を超えない限り実施例に
より何ら限定されるものではない。[Examples] The present invention will be explained in more detail below based on Examples, but the present invention is not limited by the Examples unless the gist of the invention is exceeded.
【0024】
実施例1
20μm厚のセロハンよりなる基材フィルムの接着面に
イソシアネート系アンカーコート剤を3g/m2厚みで
塗布し、この基材の上記接着面にメルトインデックス=
7g/10分、分子量分布指数=32、融点=105℃
の高圧法低密度ポリエチレン樹脂を樹脂温度315℃、
15μm厚で押出ラミネートし、この上に、上記の高圧
法低密度ポリエチレン樹脂と同様の物性を有するポリエ
チレンにステアジルジエタノールアミン0.15重量%
、グリセリンモノステアレート0.30重量%及びステ
アリルアルコール0.15重量%配合した樹脂組成物を
、樹脂温度290℃にて15μm厚で押出ラミネートし
た。
このものを温度23℃、湿度65%の条件下に保管し、
成形1週間後、1ケ月後、3ケ月後の接着強度及び表面
固有抵抗を測定した。その結果を表2に示す。尚、接着
強度及び表面固有抵抗は下記の方法により測定した。Example 1 An isocyanate-based anchor coating agent was applied at a thickness of 3 g/m2 to the adhesive surface of a base film made of cellophane with a thickness of 20 μm, and the melt index =
7g/10min, molecular weight distribution index = 32, melting point = 105°C
high pressure low density polyethylene resin at a resin temperature of 315℃,
It is extrusion laminated to a thickness of 15 μm, and on top of this, 0.15% by weight of stearyl diethanolamine is added to polyethylene having the same physical properties as the above-mentioned high-pressure low-density polyethylene resin.
A resin composition containing 0.30% by weight of glycerin monostearate and 0.15% by weight of stearyl alcohol was extrusion laminated to a thickness of 15 μm at a resin temperature of 290°C. This product was stored at a temperature of 23°C and a humidity of 65%,
Adhesive strength and surface resistivity were measured one week, one month, and three months after molding. The results are shown in Table 2. Note that the adhesive strength and surface resistivity were measured by the following method.
【0025】
(1)接着強度
25mm幅の短冊形にサンプリングした試料の一方を、
セロハンよりなる基材フィルムと高圧法低密度ポリエチ
レンとの接着面より一定距離剥がし、その剥がした部分
を万能引張試験機の上部つかみ具と下部つかみ具に取り
付け、180度方向に速度300mm/分で引張った時
の力(g/25mm幅)を接着強度とした。なお、薬包
材用途には接着強度として100g/25mm幅以上必
要である。(1) Adhesive strength One of the samples sampled in a rectangular shape with a width of 25 mm,
The base film made of cellophane and the high-pressure low-density polyethylene were peeled off a certain distance from the adhesive surface, and the peeled part was attached to the upper and lower grips of a universal tensile tester, and the film was peeled off at a speed of 300 mm/min in a 180 degree direction. The force when pulled (g/25 mm width) was defined as the adhesive strength. In addition, for use as a medicine packaging material, an adhesive strength of 100 g/25 mm width or more is required.
【0026】
(2)表面固有抵抗
JIS K6911に準拠して、安藤電気株式会社製
超絶縁抵抗計を用い、23℃、65%RHの環境下で測
定した。なお、薬包材用途には表面固有抵抗として5×
1010Ω以下必要である。(2) Surface specific resistance Measured in accordance with JIS K6911 using a super insulation resistance meter manufactured by Ando Electric Co., Ltd. in an environment of 23° C. and 65% RH. In addition, for drug packaging material use, the surface resistivity is 5×
1010Ω or less is required.
【0027】
実施例2〜3
添加剤の配合割合を第1表に示すように変えて行なった
こと以外は実施例1と同様にして行った。その結果を第
2表に示す。Examples 2 to 3 Examples 2 and 3 were carried out in the same manner as in Example 1, except that the blending ratio of additives was changed as shown in Table 1. The results are shown in Table 2.
【0028】
比較例1〜8
添加剤の配合割合を第1表に示すように変えて行なった
こと以外は実施例1と同様にして行った。その結果を第
2表に示す。Comparative Examples 1 to 8 Comparative Examples 1 to 8 Comparative Examples 1 to 8 were carried out in the same manner as in Example 1, except that the blending ratio of additives was changed as shown in Table 1. The results are shown in Table 2.
【0029】[0029]
【表1】[Table 1]
【0030】[0030]
【表2】[Table 2]
【0031】[0031]
【発明の効果】本発明により高い帯電防止効果を有する
薬包材用積層体を得ることができる。[Effects of the Invention] According to the present invention, a laminate for medicine packaging material having a high antistatic effect can be obtained.
Claims (1)
25g/cm3 以下の低密度ポリエチレン層並びに密
度が0.925g/cm3 以下の低密度ポリエチレン
に下記一般式(I)で示されるポリオキシアルキレンア
ルキルアミン0.12〜0.3重量%、高級脂肪酸グリ
セリンエステル0.25〜0.4重量%及び高級脂肪族
アルコール0.12〜0.2重量%を配合してなるポリ
エチレン樹脂組成物層を順次押出ラミネートしたもので
あって、その表面固有抵抗が5×1010Ω以下の物性
を有してなることを特徴とする薬包材用積層体 【化1】 (式中、R1 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、R2 及びR3 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。)Claim 1: At least one side of the base material has a density of 0.9.
A low density polyethylene layer having a density of 25 g/cm3 or less and a low density polyethylene having a density of 0.925 g/cm3 or less, 0.12 to 0.3% by weight of a polyoxyalkylene alkylamine represented by the following general formula (I), and higher fatty acid glycerin. Polyethylene resin composition layers containing 0.25 to 0.4% by weight of ester and 0.12 to 0.2% by weight of higher aliphatic alcohol are successively laminated by extrusion, and the surface resistivity is 5. A laminate for medicine packaging material characterized by having physical properties of ×1010 Ω or less [Formula 1] (wherein R1 is a straight or branched alkyl group having 8 to 22 carbon atoms, an oxyalkyl group, It represents an alkenyl group or an oxyalkenyl group, R2 and R3 represent an alkylene group having 2 or 3 carbon atoms, and m and n are m+n=2 to 10
represents an integer. )
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP40139690A JPH04214343A (en) | 1990-12-11 | 1990-12-11 | Laminate for cartridge agent material |
US07/809,177 US5165372A (en) | 1990-04-18 | 1991-12-18 | Steel laminate type cylinder head gasket |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP40139690A JPH04214343A (en) | 1990-12-11 | 1990-12-11 | Laminate for cartridge agent material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04214343A true JPH04214343A (en) | 1992-08-05 |
Family
ID=18511228
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP40139690A Pending JPH04214343A (en) | 1990-04-18 | 1990-12-11 | Laminate for cartridge agent material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04214343A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002212350A (en) * | 2001-01-19 | 2002-07-31 | Tosoh Corp | Resin composition for extrusion lamination and laminate produced by using the composition |
JP2010036413A (en) * | 2008-08-04 | 2010-02-18 | Tosoh Corp | Laminate film |
JP2010094911A (en) * | 2008-10-17 | 2010-04-30 | Tosoh Corp | Laminated film |
JP2011005809A (en) * | 2009-06-29 | 2011-01-13 | Tosoh Corp | Laminated film for liquid package |
JP2011016232A (en) * | 2009-07-07 | 2011-01-27 | Tosoh Corp | Laminate film |
JP2011173248A (en) * | 2010-02-23 | 2011-09-08 | Nitto Denko Corp | Antistatic laminated sheet |
-
1990
- 1990-12-11 JP JP40139690A patent/JPH04214343A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002212350A (en) * | 2001-01-19 | 2002-07-31 | Tosoh Corp | Resin composition for extrusion lamination and laminate produced by using the composition |
JP2010036413A (en) * | 2008-08-04 | 2010-02-18 | Tosoh Corp | Laminate film |
JP2010094911A (en) * | 2008-10-17 | 2010-04-30 | Tosoh Corp | Laminated film |
JP2011005809A (en) * | 2009-06-29 | 2011-01-13 | Tosoh Corp | Laminated film for liquid package |
JP2011016232A (en) * | 2009-07-07 | 2011-01-27 | Tosoh Corp | Laminate film |
JP2011173248A (en) * | 2010-02-23 | 2011-09-08 | Nitto Denko Corp | Antistatic laminated sheet |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5104109B2 (en) | Adhesive and easily peelable film using the same | |
EP2957614A1 (en) | Antistatic agent, molded article comprising insulator polymer material, and method for producing same | |
JPH04214343A (en) | Laminate for cartridge agent material | |
JP6357791B2 (en) | Easy peelable film | |
JPS6128537A (en) | Antistatic agent for polyolefin resin | |
CN108503937B (en) | Polyethylene functional master batch and preparation method thereof | |
JP2849425B2 (en) | Polyolefin resin film | |
JPH01141932A (en) | Polyolefin resin composition | |
JP3468649B2 (en) | Porous film and method for producing the same | |
JP7280029B2 (en) | Antistatic agent for polyolefin resin and polyolefin resin composition containing the same | |
JPH1121547A (en) | Antistatic agent and antistatic resin composition | |
JPH05169601A (en) | Laminate for packaging powder | |
JPS6160775A (en) | Antistatic agent composition for plastic | |
JP5397249B2 (en) | Ethylene polymer pellet mixture | |
JP4652803B2 (en) | Polylactic acid biaxially stretched film with excellent antistatic properties | |
JP2008063422A (en) | Polylactic acid-based biaxially stretched film exhibiting excellent retention of antistatic effect | |
JPH11181176A (en) | Ethylene-vinyl acetate copolymer composition with excellent antistatic properties | |
JP5917968B2 (en) | POLYMER TYPE ANTISTATIC AGENT, POLYMER COMPOSITION, AND MOLDED ARTICLE | |
JPS6411214B2 (en) | ||
JPH05500677A (en) | Polymer composition with enhanced surface energy and method for producing the same | |
JPS59217781A (en) | Antistatic agent for thermoplastic resin | |
JP2002201362A (en) | Anti-static resin composition | |
JPH0859855A (en) | Biaxially stretched polyolefin film | |
JP4678810B2 (en) | Anti-slip antistatic agent for olefin polymer film, and olefin polymer film having anti-static property and anti-slip property | |
JP2005187717A (en) | Film material |