JPH07304127A - Gas barrier packaging material and production thereof - Google Patents
Gas barrier packaging material and production thereofInfo
- Publication number
- JPH07304127A JPH07304127A JP6099461A JP9946194A JPH07304127A JP H07304127 A JPH07304127 A JP H07304127A JP 6099461 A JP6099461 A JP 6099461A JP 9946194 A JP9946194 A JP 9946194A JP H07304127 A JPH07304127 A JP H07304127A
- Authority
- JP
- Japan
- Prior art keywords
- film
- gas barrier
- packaging material
- silicon oxide
- dense
- 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
- 239000005022 packaging material Substances 0.000 title claims abstract description 26
- 230000004888 barrier function Effects 0.000 title claims abstract description 25
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000000463 material Substances 0.000 claims abstract description 28
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 25
- 238000005268 plasma chemical vapour deposition Methods 0.000 claims abstract description 11
- 239000002985 plastic film Substances 0.000 claims abstract description 8
- 229920006255 plastic film Polymers 0.000 claims abstract description 7
- 239000010408 film Substances 0.000 claims description 45
- 239000007789 gas Substances 0.000 claims description 30
- 239000010409 thin film Substances 0.000 claims description 25
- 239000000758 substrate Substances 0.000 claims description 18
- -1 silicon alkoxide Chemical class 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 5
- 239000004033 plastic Substances 0.000 claims description 5
- 229920003023 plastic Polymers 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 5
- 239000010703 silicon Substances 0.000 claims description 5
- 239000012528 membrane Substances 0.000 abstract 4
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 238000009751 slip forming Methods 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- 239000000178 monomer Substances 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 239000012495 reaction gas Substances 0.000 description 6
- 239000011888 foil Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 3
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 3
- 238000007740 vapor deposition Methods 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- KWEKXPWNFQBJAY-UHFFFAOYSA-N (dimethyl-$l^{3}-silanyl)oxy-dimethylsilicon Chemical compound C[Si](C)O[Si](C)C KWEKXPWNFQBJAY-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- NRTJGTSOTDBPDE-UHFFFAOYSA-N [dimethyl(methylsilyloxy)silyl]oxy-dimethyl-trimethylsilyloxysilane Chemical compound C[SiH2]O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C NRTJGTSOTDBPDE-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- POPWUTFDMIFIRN-UHFFFAOYSA-N bis(ethenyl)-bis(trimethylsilyloxy)silane Chemical compound C[Si](C)(C)O[Si](C=C)(C=C)O[Si](C)(C)C POPWUTFDMIFIRN-UHFFFAOYSA-N 0.000 description 1
- FSIJKGMIQTVTNP-UHFFFAOYSA-N bis(ethenyl)-methyl-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C=C)C=C FSIJKGMIQTVTNP-UHFFFAOYSA-N 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- IRWLSEJAVLQSDF-UHFFFAOYSA-N dimethyl-silyloxy-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C)O[SiH3] IRWLSEJAVLQSDF-UHFFFAOYSA-N 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- OUHONEIDEVTEIG-UHFFFAOYSA-N ethyl(methoxy)silane Chemical compound CC[SiH2]OC OUHONEIDEVTEIG-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 238000005240 physical vapour deposition Methods 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Packages (AREA)
- Wrappers (AREA)
- Laminated Bodies (AREA)
- Chemical Vapour Deposition (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、ガスバリヤー性に優れ
た包装材料およびその製造方法に関する。より詳しく
は、プラスチックフィルムやプラスチック製の立体形状
容器からなる基材上に、酸化ケイ素の薄膜を形成したガ
スバリヤー性包装材料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a packaging material excellent in gas barrier property and a method for producing the same. More specifically, the present invention relates to a gas barrier packaging material in which a thin film of silicon oxide is formed on a substrate made of a plastic film or a three-dimensional container made of plastic.
【0002】[0002]
【従来の技術】従来、水蒸気バリヤー性や酸素バリヤー
性などの、ガスバリヤー性に優れた包装材料として、金
属箔を含む積層体や金属の蒸着層を形成したプラスチッ
クフィルムを含む積層体が、広く使用されており、袋状
の容器に成形されて使用されている。そして、上記金属
としてはアルミニウムが性能、コスト、加工性の点から
一般的に使用されている。2. Description of the Related Art Conventionally, as a packaging material excellent in gas barrier properties such as water vapor barrier property and oxygen barrier property, a laminate containing a metal foil or a laminate containing a plastic film having a metal vapor deposition layer has been widely used. It is used and is molded into a bag-shaped container for use. Aluminum is generally used as the metal in terms of performance, cost, and workability.
【0003】ところが、上記金属箔や金属蒸着層はガス
バリヤー性を発揮する厚さとした場合には不透明とな
り、包装材料として使用した際に内容物が透視できない
という欠点があった。また、金属箔は、焼却したときに
炉の中で塊となってしまい、廃棄性に問題があった。さ
らに、金属を用いた包装材料は、金属探知機にかけられ
ないという欠点もあった。However, the above-mentioned metal foil or metal vapor deposition layer has a drawback that it becomes opaque when it has a thickness that exhibits gas barrier properties, and the contents cannot be seen through when used as a packaging material. Further, the metal foil becomes a lump in the furnace when incinerated, and there is a problem in disposability. Further, the packaging material using metal has a drawback that it cannot be applied to a metal detector.
【0004】金属箔や金属蒸着層の上述した欠点を克服
し、ガスバリヤー性のある材料が種々検討されている
が、酸化ケイ素の薄膜を形成したプラスチックフィルム
が、透明性、ガスバリヤー性、コストの点で優れてお
り、すでに実用化されている。Various materials having a gas barrier property have been studied by overcoming the above-mentioned drawbacks of the metal foil and the metal vapor deposition layer. However, a plastic film formed with a silicon oxide thin film has a transparency, a gas barrier property, and a cost. Is excellent and has already been put to practical use.
【0005】このような包装材料として、例えば特公昭
51−48511号公報には、酸化ケイ素の薄膜を真空
蒸着法により形成したものが記載されている。As such a packaging material, for example, Japanese Patent Publication No. 51-48511 discloses that a thin film of silicon oxide is formed by a vacuum deposition method.
【0006】また、酸化ケイ素の薄膜形成手段として、
有機シロキサンやケイ素アルコキシドと酸素の混合ガス
等の材料ガスを用いたプラズマCVD法が提案され、検
討されている。このプラズマCVD法は、真空蒸着法な
どのPVD法に比べて、膜組成の自由度が高い、立体物
への均一な薄膜形成が可能、低温で成膜が可能といった
点で優れている。Further, as a means for forming a silicon oxide thin film,
A plasma CVD method using a material gas such as an organic siloxane or a mixed gas of silicon alkoxide and oxygen has been proposed and studied. The plasma CVD method is superior to the PVD method such as the vacuum evaporation method in that it has a high degree of freedom in film composition, can form a uniform thin film on a three-dimensional object, and can form a film at a low temperature.
【0007】[0007]
【発明が解決しようとする課題】ところが、上記プラズ
マCVD法による酸化ケイ素の薄膜を形成する実験を繰
り返すうちに、本発明者らは、単純に酸化ケイ素の薄膜
を設けただけでは十分なガスバリヤー性が得られない場
合があるとの知見を得た。そして、従来から材料ガスの
組成および絶対量、反応雰囲気の真空度、RF出力等の
製膜条件を変化させることにより、酸化ケイ素の膜の組
成や密度が変化することが知られているが、本発明者ら
は、これらの組み合わせ方を特定のものとすることによ
り、当該膜が優れたガスバリヤー性を示すようになるこ
とを発見し、本発明を完成した。However, while repeating the experiment for forming a silicon oxide thin film by the plasma CVD method, the present inventors found that simply providing a silicon oxide thin film is sufficient as a gas barrier. We obtained the knowledge that there is a case that the sex is not obtained. It has been conventionally known that the composition and density of the silicon oxide film are changed by changing the film forming conditions such as the composition and absolute amount of the material gas, the vacuum degree of the reaction atmosphere, and the RF output. The inventors of the present invention discovered that the film can exhibit an excellent gas barrier property by making these combinations specific, and completed the present invention.
【0008】[0008]
【課題を解決するための手段】すなわち本発明は、基材
上にプラズマCVD法により酸化ケイ素の薄膜を形成し
てガスバリヤー性の包装材料を得る際に、該薄膜を、粗
な膜、密な膜の順の2層構造に形成することを特徴とす
るものである。Means for Solving the Problems That is, according to the present invention, when a thin film of silicon oxide is formed on a substrate by a plasma CVD method to obtain a gas barrier packaging material, the thin film is treated as a rough film or a dense film. It is characterized in that it is formed into a two-layer structure in which different films are formed in this order.
【0009】[0009]
【作用】本発明は、酸化ケイ素の薄膜を上記特定の2層
構成としたことにより、優れたガスバリヤー性を示す。The present invention exhibits excellent gas barrier properties by forming the silicon oxide thin film into the above specified two-layer structure.
【0010】[0010]
【実施例】次に、図面を参照して本発明の実施例を説明
する。図1は本発明の包装材料の一実施例を示す断面
図、図2は本発明の製造方法の説明図である。Embodiments of the present invention will now be described with reference to the drawings. FIG. 1 is a sectional view showing an embodiment of the packaging material of the present invention, and FIG. 2 is an explanatory view of the manufacturing method of the present invention.
【0011】本発明の包装材料は、基材1の少なくとも
片面に酸化ケイ素の薄膜2が形成されたものであって、
該薄膜2が、基材1上に、粗な膜21、密な膜22の順
に形成された2層構造であることを特徴とするものであ
る。The packaging material of the present invention comprises a base material 1 and a silicon oxide thin film 2 formed on at least one surface of the base material 1.
The thin film 2 has a two-layer structure in which a rough film 21 and a dense film 22 are formed in this order on the base material 1.
【0012】基材1としては、プラスチックフィルムな
いしはシート、またはプラスチック製の立体形状容器が
適用される。As the substrate 1, a plastic film or sheet or a three-dimensional container made of plastic is applied.
【0013】プラスチックの種類は特に制限ないが、ポ
リエチレン、ポリプロピレン等のポリオレフィン、ポリ
エチレンテレフタレート、ポリブチレンテレフタレー
ト、ポリエチレンナフタレート等のポリエステル、ポリ
アミド、ポリカーボネート等が使用でき、基材としてプ
ラスチックフィルムを用いる場合は一軸または二軸方向
に延伸された延伸フィルムを用いることが、耐熱性、透
明性、強度の点から好ましい。The type of plastic is not particularly limited, but polyolefins such as polyethylene and polypropylene, polyesters such as polyethylene terephthalate, polybutylene terephthalate and polyethylene naphthalate, polyamides and polycarbonates can be used. When a plastic film is used as a substrate, The use of a uniaxially or biaxially stretched film is preferable from the viewpoint of heat resistance, transparency and strength.
【0014】本発明は、上記基材1上に、酸化ケイ素の
薄膜2を、プラズマCVD法により形成する。According to the present invention, the silicon oxide thin film 2 is formed on the substrate 1 by the plasma CVD method.
【0015】プラズマCVD法自体は公知の技術である
が、本発明においては基材1として上述のようなプラス
チック製の基材1を対象としているので、耐熱性の観点
から低温で成膜できるプラズマCDV法が適している。Although the plasma CVD method itself is a known technique, in the present invention, since the plastic base material 1 as described above is used as the base material 1, a plasma which can be formed at a low temperature from the viewpoint of heat resistance. The CDV method is suitable.
【0016】より具体的には、例えば図2に示すよう
に、有機シロキサンやケイ素アルコキシド等の材料モノ
マー3を、窒素やアルゴン等の不活性ガスをキャリアー
として用い、反応ガス4である酸素と同時に対向する一
対の平板状の電極51,52を備えたチャンバー6内に
導入し、減圧下、高周波(例えば13.56MHz)の
電源を印加することにより材料ガス(材料モノマー3と
反応ガス4)をプラズマ化し、電極51,52間に配置
された基材1上に酸化ケイ素2を反応堆積させるもので
ある。More specifically, for example, as shown in FIG. 2, a material monomer 3 such as an organic siloxane or silicon alkoxide is used as a carrier with an inert gas such as nitrogen or argon, and at the same time with oxygen as a reaction gas 4. The material gas (material monomer 3 and reaction gas 4) is introduced into the chamber 6 provided with a pair of flat plate-shaped electrodes 51 and 52 facing each other, and a high frequency (eg 13.56 MHz) power source is applied under reduced pressure. It is made into plasma and the silicon oxide 2 is reactively deposited on the base material 1 arranged between the electrodes 51 and 52.
【0017】本発明において、酸化ケイ素の薄膜2を生
成するための材料モノマー3および反応ガス4として
は、公知のものが使用できるが、材料モノマー3として
は、取り扱い上の簡便さ、室温での安定性等の点から、
常温で液体状である有機シロキサンあるいはケイ素アル
コキシドを用いることが好ましい。In the present invention, as the material monomer 3 and the reaction gas 4 for forming the silicon oxide thin film 2, known materials can be used, but the material monomer 3 is easy to handle and can be used at room temperature. In terms of stability,
It is preferable to use an organic siloxane or a silicon alkoxide that is liquid at room temperature.
【0018】より具体的には、有機シロキサンとしては
ヘキサメチルジシロキサン、1,1,3,3-テトラメチルジシ
ロキサン、オクタメチルテトラシロキサン、ジビニルヘ
キサメチルトリシロキサン、ジビニルテトラメチルジシ
ロキサン、トリビニルペンタメチルトリシロキサンが使
用できる。More specifically, as the organic siloxane, hexamethyldisiloxane, 1,1,3,3-tetramethyldisiloxane, octamethyltetrasiloxane, divinylhexamethyltrisiloxane, divinyltetramethyldisiloxane, trivinyl are used. Pentamethyltrisiloxane can be used.
【0019】また、ケイ素アルコキシドとしては、ビニ
ルトリエトキシシラン、ビニルトリメトキシシラン、テ
トラメトキシシラン、テトラエトキシシラン、フェニル
トリメトキシシラン、メチルトリメトキシシラン、メチ
ルトリエトキシシラン、エチルメトキシシラン、エチル
トリメトキシシランが使用できる。As the silicon alkoxide, vinyltriethoxysilane, vinyltrimethoxysilane, tetramethoxysilane, tetraethoxysilane, phenyltrimethoxysilane, methyltrimethoxysilane, methyltriethoxysilane, ethylmethoxysilane, ethyltrimethoxy are used. Silane can be used.
【0020】そしてこの材料モノマー3は、通常、窒
素、アルゴン等の不活性ガスをキャリアーとして使用し
て、チャンバー6内に導入される。The material monomer 3 is usually introduced into the chamber 6 by using an inert gas such as nitrogen or argon as a carrier.
【0021】また、上記材料モノマー3と反応させる反
応ガス4としては、酸素を用いることが好ましい。Further, it is preferable to use oxygen as the reaction gas 4 to react with the material monomer 3.
【0022】チャンバー6内は図示しない真空ポンプに
より減圧にされる。減圧の程度(真空度)は、0.1〜
11torr程度とすることが一般的である。The inside of the chamber 6 is depressurized by a vacuum pump (not shown). Degree of vacuum (degree of vacuum) is 0.1
It is generally about 11 torr.
【0023】また、チャンバー6内には、一対の電極が
配置される。基材1がフィルム状であれば、図示のよう
に電極は平行に配置された一対の平板状電極51,52
とすることが好ましい。また、基材1が立体形状容器で
ある場合には、図示の電極52を棒状電極に変更するこ
とが好ましい。A pair of electrodes are arranged in the chamber 6. If the base material 1 is a film, the electrodes are a pair of flat plate-shaped electrodes 51, 52 arranged in parallel as shown in the figure.
It is preferable that Further, when the base material 1 is a three-dimensional container, it is preferable to change the illustrated electrode 52 to a rod-shaped electrode.
【0024】上記電極51,52間に印加する電源は、
高周波のRF電源である。この高周波は特に限定されな
いが、13.56MHzの、一般に使用されている高周
波でよい。The power source applied between the electrodes 51 and 52 is
It is a high frequency RF power supply. The high frequency is not particularly limited, but may be a commonly used high frequency of 13.56 MHz.
【0025】本発明は、上記酸化ケイ素の薄膜2の形成
に当たり、粗な膜21、密な膜22の順に、2層構造を
形成することを特徴とするものである。The present invention is characterized in that, when forming the silicon oxide thin film 2, a two-layer structure is formed in the order of the rough film 21 and the dense film 22.
【0026】上記粗な膜21は、柱状構造からなり、高
周波のRF出力を大きくすると形成されやすい傾向にあ
る。The rough film 21 has a columnar structure, and tends to be formed when the RF output of high frequency is increased.
【0027】逆に、密な膜22は、高周波のRF出力を
小さくすると形成されやすい傾向にある。On the contrary, the dense film 22 tends to be formed when the RF output of high frequency is reduced.
【0028】上記膜21,22の形成順序は本発明の目
的において重要であり、後述の実験結果からも明らかな
ように、この順とすることにより、優れたガスバリヤー
性が得られるのである。The order of forming the films 21 and 22 is important for the purpose of the present invention, and as will be apparent from the experimental results described later, this order provides excellent gas barrier properties.
【0029】これらの膜の形成は、粗な膜21を形成し
た直後に、供給ガス濃度やRF出力、真空度等の製膜条
件を変更することにより、連続して密な膜22を形成す
るようにしてもよく、あるいは、粗な膜21を形成した
後、装置から基材1を取り出し、装置の条件(例えば電
極間隔)および/または前述の製膜条件を調整して、密
な膜22を形成するようにしてもよい。In forming these films, immediately after forming the rough film 21, the film forming conditions such as the supply gas concentration, the RF output, and the degree of vacuum are changed to continuously form the dense film 22. Alternatively, after forming the rough film 21, the substrate 1 is taken out from the apparatus and the conditions of the apparatus (for example, the electrode interval) and / or the above-mentioned film forming conditions are adjusted to obtain the dense film 22. May be formed.
【0030】なお、これらの膜の厚さは、膜21は10
〜300nm、膜22は10〜200nmという範囲と
なるように、処理条件を調整することが好ましい。The thickness of these films is 10 for the film 21.
The processing conditions are preferably adjusted so that the film thickness is in the range of ˜300 nm and the film 22 is in the range of 10 to 200 nm.
【0031】反応雰囲気の温度は、必要に応じて、適宜
の手段により調節することができる。The temperature of the reaction atmosphere can be adjusted by appropriate means, if necessary.
【0032】また、基材1の温度を管理することが必要
な場合には、電極51の下部に設けたヒーターHにより
調節することができる。基材1の好ましい温度範囲は、
基材の耐熱性を考慮すると、20〜100℃である。When it is necessary to control the temperature of the substrate 1, it can be adjusted by a heater H provided below the electrode 51. The preferable temperature range of the substrate 1 is
Considering the heat resistance of the substrate, it is 20 to 100 ° C.
【0033】<実施例>図2に示したような高周波プラ
ズマCVD装置を用いて、二軸延伸ポリエチレンテレフ
タレートフィルム(25μm)を基材とし、材料ガスと
してヘキサメチルジシロキサン(HMDS)、反応ガス
として酸素(O2 )、キャリヤーガスとしてアルゴン
(Ar)を用い、前記基材上に、製膜条件を下記(表
1)のように種々変えて、1層または2層構造の酸化ケ
イ素の薄膜を形成した。なお、電極としては直径120
mmφの円形平行平板を用いた。<Example> Using a high frequency plasma CVD apparatus as shown in FIG. 2, a biaxially stretched polyethylene terephthalate film (25 μm) is used as a base material, hexamethyldisiloxane (HMDS) is used as a material gas, and a reaction gas is used. Using oxygen (O 2 ) and argon (Ar) as a carrier gas, a film of silicon oxide having a one-layer or two-layer structure was formed on the substrate by variously changing the film-forming conditions as shown in Table 1 below. Formed. The electrode has a diameter of 120.
A circular parallel plate of mmφ was used.
【0034】[0034]
【表1】 [Table 1]
【0035】得られた包装材料の、薄膜の厚さ、薄膜と
基材との密着強度、および包装材料の酸素透過度を測
定、評価した。結果を表2に示す。The thickness of the thin film of the obtained packaging material, the adhesion strength between the thin film and the substrate, and the oxygen permeability of the packaging material were measured and evaluated. The results are shown in Table 2.
【0036】ここで、薄膜の厚さは、得られた包装材料
を切断してその断面を透過型電子顕微鏡にて撮影、測定
した。薄膜と基材との密着強度は、セロハンテープによ
る引きはがし試験(JISH8504)に準拠して行
い、膜の剥離度合いで評価した。また、包装材料の酸素
透過度は、モダンコントロールズ社製のOX−TRAN
10/50という装置を用いて、20℃、100%RH
という方法で測定した(単位:cc/m2・day )。Here, the thickness of the thin film was measured by cutting the obtained packaging material and photographing its cross section with a transmission electron microscope. The adhesion strength between the thin film and the substrate was measured according to the peeling test using cellophane tape (JIS H8504), and the peeling degree of the film was evaluated. The oxygen permeability of the packaging material is OX-TRAN manufactured by Modern Controls.
10/50 equipment, 20 ℃, 100% RH
It was measured by the method (unit: cc / m 2 · day).
【0037】なお、得られた包装材料はいずれも無色透
明であった。The packaging materials obtained were all colorless and transparent.
【0038】[0038]
【表2】 [Table 2]
【0039】上述の結果からわかるように、本発明の、
「粗な膜/密な膜」の順に形成した薄膜(No. 1〜5)
は、一層のみ形成したもの(No. 6,7)や他の順に形
成したもの(No. 8〜10)に比べ、優れたガスバリヤ
ー性を示すことがわかる。As can be seen from the above results, according to the present invention,
Thin films (No. 1-5) formed in order of "rough film / dense film"
It can be seen that shows excellent gas barrier properties as compared with those formed only in one layer (No. 6, 7) and those formed in other orders (No. 8 to 10).
【0040】[0040]
【発明の効果】以上述べたように、本発明は、基材上に
プラズマCVD法により形成する酸化ケイ素の薄膜を、
粗な膜、密な膜の順の2層構造に形成するという構成を
採用したことにより、包装材料に優れたガスバリヤー性
と、高い透明性を与えることができた。また、本発明は
平坦なフィルム、シートばかりでなく、立体形状のボト
ルやトレーといった成形物にも適用ができる。そして、
得られた包装材料は、アルミニウム箔を使用する必要が
なく、従って廃棄性にも優れるものである。As described above, according to the present invention, a thin film of silicon oxide formed on a substrate by the plasma CVD method,
By adopting a structure in which a rough film and a dense film are formed in the order of two layers, excellent gas barrier properties and high transparency can be given to the packaging material. Further, the present invention can be applied not only to flat films and sheets but also to molded products such as three-dimensional bottles and trays. And
The obtained packaging material does not require the use of aluminum foil and is therefore excellent in disposability.
【図面の簡単な説明】[Brief description of drawings]
【図1】本発明の包装材料の一実施例を示す断面図であ
る。FIG. 1 is a cross-sectional view showing an example of a packaging material of the present invention.
【図2】本発明の製造方法の一実施例を示す説明図であ
る。FIG. 2 is an explanatory view showing an embodiment of the manufacturing method of the present invention.
1……基材 2……酸化ケイ素の薄膜 21…酸化ケイ素の粗な膜21 22…酸化ケイ素の密な膜21 3……材料モノマー 4……反応ガス 51、52…電極 6……チャンバー 1 ... Substrate 2 ... Silicon oxide thin film 21 ... Silicon oxide rough film 21 22 ... Silicon oxide dense film 21 3 ... Material monomer 4 ... Reaction gas 51,52 ... Electrode 6 ... Chamber
─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───
【手続補正書】[Procedure amendment]
【提出日】平成6年6月1日[Submission date] June 1, 1994
【手続補正1】[Procedure Amendment 1]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0022[Name of item to be corrected] 0022
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0022】チャンバー内6は図示しない真空ポンプに
より減圧にされる。減圧の程度(真空度)は、0.1〜
1torr程度とすることが一般的である。The chamber 6 is depressurized by a vacuum pump (not shown). Degree of vacuum (degree of vacuum) is 0.1
It is generally about 1 torr.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C23C 16/40 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location C23C 16/40
Claims (6)
が形成されたガスバリヤー性包装材料であって、該薄膜
が、基材上に、粗な膜、密な膜の順に形成された2層構
造であることを特徴とする、ガスバリヤー性包装材料。1. A gas barrier packaging material in which a thin film of silicon oxide is formed on at least one side of a substrate, wherein the thin film is formed on a substrate in the order of a rough film and a dense film. A gas barrier packaging material having a layered structure.
1に記載のガスバリヤー性包装材料。2. The gas barrier packaging material according to claim 1, wherein the rough film is a film having a columnar structure.
1に記載のガスバリヤー性包装材料。3. The gas barrier packaging material according to claim 1, wherein the substrate is a plastic film.
る請求項1に記載のガスバリヤー性包装材料。4. The gas barrier packaging material according to claim 1, wherein the substrate is a three-dimensional container made of plastic.
が形成されたガスバリヤー性包装材料の製造方法であっ
て、基材上に、プラズマCVD法により酸化ケイ素の粗
な膜を形成し、この粗な膜上に、プラズマCVD法によ
り酸化ケイ素の密な膜を形成することを特徴とする、ガ
スバリヤー性包装材料の製造方法。5. A method for producing a gas barrier packaging material in which a thin film of silicon oxide is formed on at least one surface of a base material, wherein a rough film of silicon oxide is formed on the base material by a plasma CVD method. A method for producing a gas barrier packaging material, characterized in that a dense film of silicon oxide is formed on the rough film by a plasma CVD method.
アルコキシドのいずれかのガスと、酸素との混合ガスで
あることを特徴とする、請求項5に記載の方法。6. The method according to claim 5, wherein the material gas is a mixed gas of either an organic siloxane gas or a silicon alkoxide gas and oxygen.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6099461A JPH07304127A (en) | 1994-05-13 | 1994-05-13 | Gas barrier packaging material and production thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6099461A JPH07304127A (en) | 1994-05-13 | 1994-05-13 | Gas barrier packaging material and production thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH07304127A true JPH07304127A (en) | 1995-11-21 |
Family
ID=14247960
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6099461A Pending JPH07304127A (en) | 1994-05-13 | 1994-05-13 | Gas barrier packaging material and production thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07304127A (en) |
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