JP2000318080A - Conductive sheet - Google Patents
Conductive sheetInfo
- Publication number
- JP2000318080A JP2000318080A JP11126850A JP12685099A JP2000318080A JP 2000318080 A JP2000318080 A JP 2000318080A JP 11126850 A JP11126850 A JP 11126850A JP 12685099 A JP12685099 A JP 12685099A JP 2000318080 A JP2000318080 A JP 2000318080A
- Authority
- JP
- Japan
- Prior art keywords
- conductive
- sheet
- layer
- agent
- ion
- 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
- 230000004888 barrier function Effects 0.000 claims abstract description 27
- 239000006258 conductive agent Substances 0.000 claims abstract description 27
- 229910001410 inorganic ion Inorganic materials 0.000 claims abstract description 24
- 239000002216 antistatic agent Substances 0.000 claims abstract description 13
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract description 15
- 239000011248 coating agent Substances 0.000 abstract description 8
- 238000000576 coating method Methods 0.000 abstract description 8
- 229920001940 conductive polymer Polymers 0.000 abstract description 5
- 238000000034 method Methods 0.000 abstract description 5
- 239000004020 conductor Substances 0.000 abstract description 4
- 239000002904 solvent Substances 0.000 abstract description 3
- 229920005992 thermoplastic resin Polymers 0.000 abstract description 2
- 238000005342 ion exchange Methods 0.000 abstract 3
- 239000007788 liquid Substances 0.000 abstract 2
- 150000002500 ions Chemical class 0.000 description 25
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
- -1 halogen ion Chemical class 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000006185 dispersion Substances 0.000 description 8
- 239000002585 base Substances 0.000 description 7
- 150000001768 cations Chemical class 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000002985 plastic film Substances 0.000 description 4
- 229920001225 polyester resin Polymers 0.000 description 4
- 239000004645 polyester resin Substances 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920005749 polyurethane resin Polymers 0.000 description 3
- 125000001453 quaternary ammonium group Chemical group 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Chemical compound [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 2
- 229920000128 polypyrrole Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- ZPFAVCIQZKRBGF-UHFFFAOYSA-N 1,3,2-dioxathiolane 2,2-dioxide Chemical compound O=S1(=O)OCCO1 ZPFAVCIQZKRBGF-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- 229920008790 Amorphous Polyethylene terephthalate Polymers 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229940044631 ferric chloride hexahydrate Drugs 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NQXWGWZJXJUMQB-UHFFFAOYSA-K iron trichloride hexahydrate Chemical compound O.O.O.O.O.O.[Cl-].Cl[Fe+]Cl NQXWGWZJXJUMQB-UHFFFAOYSA-K 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910001416 lithium ion Inorganic materials 0.000 description 1
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 description 1
- 229910001486 lithium perchlorate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Non-Insulated Conductors (AREA)
- Packages (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、導電性シートに関
し、更に詳しくは各種電子部品の包装等に有用な導電性
シートに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a conductive sheet, and more particularly, to a conductive sheet useful for packaging various electronic parts.
【0002】[0002]
【従来の技術】従来、IC、コンデンサ、トランジス
タ、LSI等の各種電子部品は、キャリヤーテープやキ
ャリヤートレイ等と称される、プラスチックシートを所
望の形状に成形した容器に封入されて保管及び輸送等が
為されている。上記電子部品等は静電気のスパーク等に
よって容易に破壊され易い。そのために、上記キャリヤ
ーテープ等に使用するプラスチックシートには導電層や
帯電防止層が形成され、若しくはシート中に導電剤や帯
電防止剤を混入して該シートを導電性(帯電防止性)と
している。2. Description of the Related Art Conventionally, various electronic components such as ICs, capacitors, transistors, and LSIs are stored and transported in a container formed by molding a plastic sheet into a desired shape called a carrier tape or a carrier tray. Has been made. The electronic components and the like are easily broken by static electricity sparks or the like. Therefore, a conductive layer or an antistatic layer is formed on the plastic sheet used for the carrier tape or the like, or a conductive agent or an antistatic agent is mixed into the sheet to make the sheet conductive (antistatic). .
【0003】上記導電剤或いは帯電防止剤としては、導
電性カーボンブラック、導電性金属酸化物、金属粉等の
電子伝導性材料や、例えば、第四級アンモニウム基を有
する界面活性剤、或いはポリピロール、ポリウレタン、
アクリル樹脂、ポリエステル樹脂等に低分子の電解質を
ドーピングしたイオン導電性ポリマー、或いはこれらの
ポリマーに第4級アンモニウム基を導入したポリマー等
の有機物が使用されている。導電性カーボンブラック以
外の上記の電子伝導性導電剤は一般に性能に比較して高
価であり、又、その使用方法も容易とはいえず、又、導
電性カーボンブラックは強く着色されているので、その
使用は外観的或いは商品的には望ましくない場合が多
い。Examples of the conductive agent or antistatic agent include electronic conductive materials such as conductive carbon black, conductive metal oxides and metal powders, and surfactants having a quaternary ammonium group, polypyrrole, and the like. Polyurethane,
An organic material such as an ion conductive polymer obtained by doping a low molecular electrolyte into an acrylic resin or a polyester resin, or a polymer having a quaternary ammonium group introduced into these polymers is used. The above-mentioned electron conductive conductive agents other than conductive carbon black are generally expensive compared to their performance, and their use is not easy, and since conductive carbon black is strongly colored, Its use is often undesirable in appearance or in commercial terms.
【0004】[0004]
【発明が解決しようとしている課題】電子伝導性材料と
は異なり、前記のイオン導電性導電剤は、多くの場合安
価で且つ無色であり、又、有機物であることから、帯電
防止剤として使用し易く、広範な分野で使用されてい
る。使用の形態としては、基材シートであるプラスチッ
クシートの表面に導電層又は帯電防止層を形成する態様
と、プラスチック中に練り込み、その後にシート化され
る形態がある。このような導電性シートは製造が容易で
且つ安価であるが、該シートを電子部品の包装等に使用
した場合には、導電性を発現しているアルカリ金属等の
カチオンや、その対イオンであるハロゲンイオン、硫酸
エステルイオン等の酸のイオンが電子部品に移行するこ
とがあり、そのために電子部品が発錆等の損傷を受ける
場合があって、その使用は一定の制限を受けている。従
って本発明の目的は、導電剤若しくは帯電防止剤として
イオン導電性材料を使用した場合にも、電子部品に損傷
を与えることがない導電性シートを提供することであ
る。Unlike the electron conductive material, the ionic conductive agent is inexpensive and colorless in many cases, and because it is an organic substance, it is used as an antistatic agent. Easy and widely used. As a form of use, there are a form in which a conductive layer or an antistatic layer is formed on the surface of a plastic sheet as a base material sheet, and a form in which a plastic sheet is kneaded into a plastic and then formed into a sheet. Such a conductive sheet is easy and inexpensive to manufacture, but when the sheet is used for packaging electronic components, etc., the cation such as an alkali metal exhibiting conductivity or a counter ion thereof is used. An acid ion such as a halogen ion or a sulfate ion ion may be transferred to an electronic component, which may damage the electronic component, such as rust, and its use is subject to certain restrictions. Therefore, an object of the present invention is to provide a conductive sheet which does not damage electronic components even when an ion conductive material is used as a conductive agent or an antistatic agent.
【0005】[0005]
【課題を解決するための手段】上記目的は以下の本発明
によって達成される。即ち、本発明は、少なくとも一方
の面に導電層又は帯電防止層が設けられた導電性シート
において、上記導電層又は帯電防止層の表面に無機イオ
ン交換体を含むイオンバリヤー層が形成されていること
を特徴とする導電性シート、及び導電剤及び/又は帯電
防止剤を含む導電性シートの少なくとも一方の表面に無
機イオン交換体を含むイオンバリヤー層が形成されてい
ることを特徴とする導電性シートを提供する。The above object is achieved by the present invention described below. That is, in the present invention, in a conductive sheet provided with a conductive layer or an antistatic layer on at least one surface, an ion barrier layer containing an inorganic ion exchanger is formed on the surface of the conductive layer or the antistatic layer. A conductive sheet, characterized in that an ion barrier layer containing an inorganic ion exchanger is formed on at least one surface of a conductive sheet and a conductive sheet containing a conductive agent and / or an antistatic agent. Provide a sheet.
【0006】本発明によれば、導電性シートの表面に無
機イオン交換体を含むイオンバリヤー層を形成すること
によって、導電性シートから移行してくる各種イオンに
よる電子部品の汚染や損傷を防止することができる。
尚、本発明は導電剤がイオン性導電剤である場合に限ら
れず、導電剤が電子伝導導電剤である場合にも勿論有効
である。According to the present invention, by forming an ion barrier layer containing an inorganic ion exchanger on the surface of a conductive sheet, contamination and damage to electronic components due to various ions migrating from the conductive sheet are prevented. be able to.
The present invention is not limited to the case where the conductive agent is an ionic conductive agent, but is of course effective when the conductive agent is an electron conductive conductive agent.
【0007】[0007]
【発明の実施の形態】次に好ましい実施の形態を挙げて
本発明を更に詳細に説明する。図1は、本発明の導電性
シートの一形態を示す図であり、図2は他の形態を示す
図である。図1に示す例の導電性シートは、導電層2が
設けられた基材シート1において、上記導電層2の表面
に無機イオン交換体を含むイオンバリヤー層3が形成さ
れている。図2に示す例の導電性シートは、導電剤を含
む導電性シート4の少なくとも一方の表面に無機イオン
交換体を含むイオンバリヤー層3が形成されている。
尚、図2に示す例では導電性シートの両面にイオンバリ
ヤー層が形成されているが、その形成は一方の面のみで
もよい。Next, the present invention will be described in more detail with reference to preferred embodiments. FIG. 1 is a diagram illustrating one embodiment of the conductive sheet of the present invention, and FIG. 2 is a diagram illustrating another embodiment. In the conductive sheet of the example shown in FIG. 1, an ion barrier layer 3 containing an inorganic ion exchanger is formed on the surface of the conductive layer 2 in a base sheet 1 provided with a conductive layer 2. In the conductive sheet of the example shown in FIG. 2, an ion barrier layer 3 containing an inorganic ion exchanger is formed on at least one surface of a conductive sheet 4 containing a conductive agent.
In the example shown in FIG. 2, the ion barrier layers are formed on both sides of the conductive sheet, but the formation may be performed on only one side.
【0008】本発明で使用するプラスチック基材シート
としては、例えば、ポリエチレンテレフタレート等のポ
リエステル樹脂、ポリプロピレン樹脂、ポリカーボネー
ト樹脂、ポリスチレン樹脂、ポリ塩化ビニル樹脂、ポリ
アミド樹脂等の一般的な熱可塑性樹脂からなるシートで
あり、その厚みは特に限定されないが、一般的には0.
2〜1.5mm程度である。The plastic substrate sheet used in the present invention is made of, for example, a general thermoplastic resin such as a polyester resin such as polyethylene terephthalate, a polypropylene resin, a polycarbonate resin, a polystyrene resin, a polyvinyl chloride resin and a polyamide resin. The sheet is not particularly limited in thickness, but generally has a thickness of 0.1 mm.
It is about 2 to 1.5 mm.
【0009】図1に示す例では、上記基材シート1の少
なくとも一方の面に導電層2を形成する。ここで使用す
る導電剤としては、前記電子伝導性の導電剤であっても
よいが、本発明は、導電剤がイオン導電性の帯電防止剤
や導電性ポリマーである場合に特に効果的である。帯電
防止剤又は導電性ポリマーとしては、第4級アンモニウ
ム基を有する界面活性剤や高分子化合物、或いは各種高
分子材料に電解質をドーピングしてなる導電性高分子が
挙げられる。尚、以下では導電剤及び帯電防止剤を纏め
て導電剤といい、導電層及び帯電防止層を纏めて導電層
という。In the example shown in FIG. 1, a conductive layer 2 is formed on at least one surface of the base sheet 1. The conductive agent used here may be the above-mentioned electron conductive conductive agent, but the present invention is particularly effective when the conductive agent is an ion conductive antistatic agent or a conductive polymer. . Examples of the antistatic agent or the conductive polymer include a surfactant or a polymer compound having a quaternary ammonium group, or a conductive polymer obtained by doping various polymer materials with an electrolyte. Hereinafter, the conductive agent and the antistatic agent are collectively referred to as a conductive agent, and the conductive layer and the antistatic layer are collectively referred to as a conductive layer.
【0010】導電層の形成は特に限定されず、公知の方
法がそのまま使用される。例えば、導電剤が低分子量の
界面活性剤等の如く、それ自体では皮膜形成能がない場
合には、適当な皮膜形成材、例えば、アクリル樹脂、ポ
リエステル樹脂、ポリウレタン樹脂、塩化ビニル又は酢
酸ビニルの単独重合体又は他のモノマーとの共重合体等
を用いて導電層を形成する。通常は適当な溶剤中に導電
剤及び皮膜形成材を分散・溶解して塗布液を調製し、こ
れを基材シートに塗布及び乾燥して導電層を形成する。The formation of the conductive layer is not particularly limited, and a known method can be used as it is. For example, if the conductive agent is not capable of forming a film by itself, such as a low molecular weight surfactant, a suitable film forming material, for example, acrylic resin, polyester resin, polyurethane resin, vinyl chloride or vinyl acetate A conductive layer is formed using a homopolymer, a copolymer with another monomer, or the like. Usually, a conductive agent and a film forming material are dispersed and dissolved in an appropriate solvent to prepare a coating solution, which is applied to a substrate sheet and dried to form a conductive layer.
【0011】一方、導電剤が高分子導電剤である場合に
は、必ずしも皮膜形成剤の使用は必須ではないが、基材
シートに対する密着性や皮膜の強度を上げるために、皮
膜形成材を用いることが好ましい。導電層の形成方法は
前記と同様である。このように形成する導電層の厚みは
特に限定されないが、通常は1〜5μm程度であり、そ
の表面抵抗の範囲は102〜1010Ω/cm程度の範囲
とする。図2に示す例の場合には、前記の如き基材シー
ト用プラスチック材料に、予め上記の如き所定の表面抵
抗値を発現する量の導電剤を溶融混練し、これを常法に
従ってシート化すればよい。On the other hand, when the conductive agent is a polymer conductive agent, it is not always necessary to use a film forming agent, but a film forming material is used to increase the adhesion to the base sheet and the strength of the film. Is preferred. The method for forming the conductive layer is the same as described above. The thickness of the conductive layer thus formed is not particularly limited, but is usually about 1 to 5 μm, and its surface resistance is in the range of about 10 2 to 10 10 Ω / cm. In the case of the example shown in FIG. 2, an amount of a conductive agent that expresses a predetermined surface resistance value as described above is melt-kneaded in advance with the plastic material for a base sheet as described above, and this is formed into a sheet according to a conventional method. I just need.
【0012】本発明では、上記の如き導電性シートの表
面に無機イオン交換体を含むイオンバリヤー層3を形成
する。該バリヤー層は、図1の例では基材シートの一方
の面に形成され、図2に示す例では、導電性シートの両
面に形成されているが、目的とする導電性シートの用途
に従って、何れの場合も一方の面又は両面に形成するこ
とができる。In the present invention, an ion barrier layer 3 containing an inorganic ion exchanger is formed on the surface of the conductive sheet as described above. The barrier layer is formed on one surface of the base sheet in the example of FIG. 1, and is formed on both surfaces of the conductive sheet in the example shown in FIG. 2, but according to the intended use of the conductive sheet, In any case, it can be formed on one surface or both surfaces.
【0013】本発明で使用する無機イオン交換体自体は
公知の材料であり、例えば、「阿部光雄、Japan Analys
t, 23, 1254及び1561(1974)」、特開昭60−1685
41号公報、特開昭60−172353号公報、特開昭
63−1452号公報、特開昭63−60112号公
報、特開平3−4940号公報、特開平4−45854
号公報等に記載されており、又、これらの文献に記載さ
れた無機イオン交換体に種々の処理を加えたものでもよ
い。具体的には、商品名「IXE」−100、150、
200、300、400、500、550、600、8
00、680、700、702、900、1000、1
100、1320等の商品名で、例えば、東亜合成化学
工業株式会社等から入手して本発明で使用することがで
きる。特にマグネシウム−アルミニウム系、アンチモン
系、カルシウム系等の無機イオン交換体が有用である。The inorganic ion exchanger used in the present invention is a known material, for example, “Mitsuo Abe, Japan Analys
t, 23, 1254 and 1561 (1974) ", JP-A-60-1685.
No. 41, JP-A-60-172353, JP-A-63-1452, JP-A-63-60112, JP-A-3-4940, JP-A-4-45854
And various treatments may be added to the inorganic ion exchanger described in these documents. Specifically, the product name “IXE” -100, 150,
200, 300, 400, 500, 550, 600, 8
00, 680, 700, 702, 900, 1000, 1
Under the trade names of 100, 1320, etc., for example, it can be obtained from Toa Gosei Chemical Industry Co., Ltd. or the like and used in the present invention. Particularly, inorganic ion exchangers such as magnesium-aluminum-based, antimony-based, and calcium-based are useful.
【0014】上記無機イオン交換体を用いてイオンバリ
ヤー層を形成する方法としては、適当な皮膜形成材、例
えば、アクリル樹脂、ポリエステル樹脂、ポリウレタン
樹脂、塩化ビニル又は酢酸ビニルの単独重合体又は他の
モノマーとの共重合体等の皮膜形成材を、例えば、イソ
ピロピルアルコール等のアルコール系、メチルエチルケ
トン、メチルイソブチルケトン、シクロヘキサノン等の
ケトン系溶剤、トルエン、キシレン等の芳香族系溶剤、
アミド系溶剤或いはこれらの混合系溶剤に、無機イオン
交換体とともに加え、両者を分散・溶解して塗布液を調
製し、これを導電層2又は導電性シート4の表面に塗布
及び乾燥して形成すればよい。As a method of forming an ion barrier layer using the above-mentioned inorganic ion exchanger, a suitable film-forming material, for example, an acrylic resin, a polyester resin, a polyurethane resin, a homopolymer of vinyl chloride or vinyl acetate, or another polymer may be used. Film-forming materials such as copolymers with monomers, for example, alcohols such as isopropyl alcohol, methyl ethyl ketone, methyl isobutyl ketone, ketone solvents such as cyclohexanone, toluene, aromatic solvents such as xylene,
An inorganic ion exchanger is added to an amide solvent or a mixed solvent thereof together with an inorganic ion exchanger, and both are dispersed and dissolved to prepare a coating solution, which is applied to the surface of the conductive layer 2 or the conductive sheet 4 and dried to form a coating solution. do it.
【0015】形成されるイオンバリヤー層における無機
イオン交換体の含有量は皮膜形成材100重量部当たり
約10〜30重量部の範囲が好ましく、無機イオン交換
体の濃度が低過ぎると十分なイオンバリヤー性が得られ
ず、一方、無機イオン交換体の量が多すぎると、十分に
強靭な皮膜が形成されず、無機イオン交換体の脱落等が
生じ、かえって電子部品を汚染するおそれがある。又、
形成されるイオンバリヤー層の厚みは約1〜3μm程度
が好ましい。イオンバリヤー層が薄すぎると、十分なバ
リヤー性が得られず、又、導電性シートを適当な形状に
成形する時にそのコーナー部等においてバリヤー層が薄
くなり、部分的にバリヤー性が低下する。一方、イオン
バリヤー層が厚過ぎても特別に性能が向上することはな
く、コスト面において不利である。The content of the inorganic ion exchanger in the formed ion barrier layer is preferably in the range of about 10 to 30 parts by weight per 100 parts by weight of the film-forming material. If the concentration of the inorganic ion exchanger is too low, a sufficient ion barrier is obtained. On the other hand, if the amount of the inorganic ion exchanger is too large, a sufficiently tough film is not formed, the inorganic ion exchanger may fall off, and the electronic components may be contaminated. or,
The thickness of the formed ion barrier layer is preferably about 1 to 3 μm. If the ion barrier layer is too thin, sufficient barrier properties cannot be obtained, and when forming the conductive sheet into an appropriate shape, the barrier layer becomes thin at corners and the like, and the barrier properties are partially reduced. On the other hand, if the ion barrier layer is too thick, the performance is not particularly improved, which is disadvantageous in cost.
【0016】以上の如くして得られた本発明の導電性シ
ートは、各種電子部品のキャリヤーテープやトレイ等の
各種包装材の原反として有用であり、使用に際しては必
要に応じて真空成形等により所望の形状に成形する。こ
の際、電子部品が接触する面はイオンバリヤー層の面と
することが必要である。このように電子部品を包装する
ことによって、導電層中に存在しているリチウム、カリ
ウム、ナトリウム等の陽イオンが導電層の表面に移行し
た場合には、イオンバリヤー層中の無機イオン交換体に
よってプロトンと置換されるので、これらの陽イオンが
電子部品に接触して汚染することがない。又、導電層中
に存在している塩素イオン等のハロゲンイオン、硫酸エ
ステルイオン、硝酸イオン、過塩素酸イオン等の陰イオ
ンが導電層の表面に移行した場合には、イオンバリヤー
層中の無機イオン交換体によって水酸基イオンと置換さ
れるので、これらの陰イオンが電子部品に接触して電子
部品を発錆させたり、汚染したりすることがない。The conductive sheet of the present invention obtained as described above is useful as a raw material for various packaging materials such as carrier tapes and trays for various electronic components. To form a desired shape. At this time, it is necessary that the surface in contact with the electronic component be the surface of the ion barrier layer. When the cations such as lithium, potassium, and sodium present in the conductive layer migrate to the surface of the conductive layer by packaging the electronic component in this way, the inorganic ion exchanger in the ion barrier layer transfers the cations. Since these cations are replaced with protons, these cations do not contact and contaminate the electronic component. Also, when anions such as chloride ions and the like, sulfate ions, nitrate ions, perchlorate ions and the like existing in the conductive layer migrate to the surface of the conductive layer, inorganic ions in the ion barrier layer may be removed. Since the hydroxyl group ions are replaced by the ion exchanger, these anions do not come into contact with the electronic component to rust or contaminate the electronic component.
【0017】[0017]
【実施例】次に実施例及び比較例を挙げて本発明を更に
具体的に説明する。尚、文中部又は%とあるのは特に断
りのない限り重量基準である。 1.ポリウレタン樹脂15部、トルエン35部及びメチ
ルエチルケトン50部からなる樹脂溶液100部に、ア
ルキルアンモニウムエトサルフェート5部を加えて撹拌
し、均一な導電層形成用溶液(溶液A)とした。この溶
液Aはカチオンであるアルキル第4級アンモニウム塩
と、アニオンであるアルキル硫酸エステルとを当量含有
している。Next, the present invention will be described more specifically with reference to examples and comparative examples. In the following, "parts" and "%" are based on weight unless otherwise specified. 1. To 100 parts of a resin solution comprising 15 parts of a polyurethane resin, 35 parts of toluene and 50 parts of methyl ethyl ketone, 5 parts of alkylammonium ethosulfate was added and stirred to obtain a uniform conductive layer forming solution (solution A). This solution A contains an equivalent amount of an alkyl quaternary ammonium salt as a cation and an alkyl sulfate ester as an anion.
【0018】2.2000部の水に8部のメチルセルロ
ースを溶解させた液に10部の6水和塩化第二鉄を溶解
させる。この液に2.4部のピロールを良く撹拌しなが
ら加えてピロールの酸化重合を行ない、ポリピロールの
分散液(溶液B)を調製した。この溶液Bは、酸化の鉄
イオンと、これと当量の塩素イオンを含有している。 3.過塩素酸リチウム7部を配位したポリエチレングリ
コール(分子量2,000)70部に1,4−ブタンジ
オール10部を加えた混合物を、ジメチルホルムアミド
50部及びメチルエチルケトン140部との混合溶剤に
溶解させる。次に4,4’−ジフェニルメタンジイソシ
アネートを徐々に添加しながら溶液の粘度が20℃で2
00ポイズになるまで反応させる。反応終了後、この溶
液をメチルエチルケトンにて固形分が13%になるよう
に希釈する。この希釈液を溶液Cとする。この溶液Cに
はリチウムイオンと過塩素酸イオンを当量づつ含有して
いる。2. Dissolve 10 parts of ferric chloride hexahydrate in a solution of 8 parts of methylcellulose in 2000 parts of water. To this solution, 2.4 parts of pyrrole was added with good stirring to carry out oxidative polymerization of pyrrole to prepare a polypyrrole dispersion (solution B). This solution B contains oxidized iron ions and equivalent amounts of chloride ions. 3. A mixture obtained by adding 10 parts of 1,4-butanediol to 70 parts of polyethylene glycol (molecular weight: 2,000) coordinated with 7 parts of lithium perchlorate is dissolved in a mixed solvent of 50 parts of dimethylformamide and 140 parts of methyl ethyl ketone. . Then, while gradually adding 4,4′-diphenylmethane diisocyanate, the viscosity of
React until 00 poise. After the completion of the reaction, this solution is diluted with methyl ethyl ketone to a solid content of 13%. This diluted solution is referred to as solution C. This solution C contains lithium ions and perchlorate ions in equivalent amounts.
【0019】4.塩化ビニル−アクリル共重合ポリマー
15部をトルエン35部及びメチルエチルケトン50部
に溶解させ、溶液Dとする。 5.溶液D100部に下記表1の無機イオン交換体をそ
れぞれ3部づつ添加して十分に分散させる。この分散液
を分散液D1、D2及びD3とする。 4. 15 parts of a vinyl chloride-acryl copolymer is dissolved in 35 parts of toluene and 50 parts of methyl ethyl ketone to prepare a solution D. 5. To 100 parts of solution D, 3 parts of each of the inorganic ion exchangers shown in Table 1 below were added and dispersed sufficiently. This dispersion is referred to as dispersions D1, D2, and D3.
【0020】例1 厚さ0.5mmの無定形ポリエチレンテレフタレートシ
ートの表面に前記溶液Aをグラビアコート法により乾燥
時塗布厚みが1g/m2になる割合で塗布及び乾燥して
導電層を形成して導電性シート(イ)とした。この導電
性シート(イ)の温度20℃×湿度70%における表面
抵抗は108/□であった。この導電性シート(イ)の
導電層の表面に前記分散液Dを乾燥時膜厚が0.8g/
m2になる割合で塗布及び乾燥して層を形成し、比較例
の導電性シート(イ−D)とした。Example 1 The above solution A was applied to the surface of an amorphous polyethylene terephthalate sheet having a thickness of 0.5 mm by a gravure coating method at a rate of a coating thickness of 1 g / m 2 when dried to form a conductive layer. Thus, a conductive sheet (a) was obtained. The surface resistance of this conductive sheet (a) at a temperature of 20 ° C. and a humidity of 70% was 10 8 / □. On the surface of the conductive layer of the conductive sheet (a), the dispersion D was dried to have a film thickness of 0.8 g /
The layer was formed by coating and drying at a ratio of m 2 to obtain a conductive sheet (ID) of Comparative Example.
【0021】例2 分散液Dに代えて、前記分散液D1、D2及びD3をそ
れぞれ使用し、他は例1と同様にして、本発明の導電性
シート(イ−D1)、導電性シート(イ−D2)及び導
電性シート(イ−D3)を得た。Example 2 In place of Dispersion D, Dispersions D1, D2 and D3 were respectively used, and the others were the same as in Example 1, except that the conductive sheet (a-D1), A-D2) and a conductive sheet (A-D3) were obtained.
【0022】例3 厚さ0.7mmのポリスチレンシートの表面に、前記溶
液Bを、乾燥時塗布厚みが0.8g/m2になる割合で
塗布及び乾燥して導電層を形成して導電性シート(ロ)
とした。この導電性シート(ロ)の温度20℃×湿度7
0%における表面抵抗は106/□であった。この導電
性シート(ロ)の導電層の表面に、例1、2におけると
同様にして前記分散液D、D1、D2及びD3を乾燥時
膜厚が0.8g/m2になる割合で塗布及び乾燥して、
比較例の導電性シート(ロ−D)、本発明の導電性シー
ト(ロ−D1)、導電性シート(ロ−D2)及び導電性
シート(ロ−D3)を得た。Example 3 The above solution B was applied to the surface of a 0.7 mm thick polystyrene sheet at a rate of 0.8 g / m 2 when dried to form a conductive layer. Seat (b)
And The temperature of this conductive sheet (b) 20 ° C x humidity 7
The surface resistance at 0% was 10 6 / □. The dispersions D, D1, D2, and D3 were applied to the surface of the conductive layer of the conductive sheet (b) in the same manner as in Examples 1 and 2 at a rate such that the film thickness when dried was 0.8 g / m 2. And dry,
The conductive sheet (b-D) of the comparative example, the conductive sheet (b-D1), the conductive sheet (b-D2), and the conductive sheet (b-D3) of the present invention were obtained.
【0023】例4 厚さ0.4mmのポリ塩化ビニルシートの表面に、前記
溶液Cを、乾燥時塗布厚みが1g/m2になる割合でグ
ラビア方式で塗布及び乾燥して導電層を形成して導電性
シート(ハ)とした。この導電性シート(ハ)の温度2
0℃×湿度70%における表面抵抗は106/□であっ
た。この導電性シート(ハ)の導電層の表面に、例1、
2におけると同様にして前記分散液D、D1、D2及び
D3を乾燥時膜厚が0.8g/m2になる割合で塗布及
び乾燥して比較例の導電性シート(ハ−D)、本発明の
導電性シート(ハ−D1)、導電性シート(ハ−D2)
及び導電性シート(ハ−D3)を得た。Example 4 On the surface of a polyvinyl chloride sheet having a thickness of 0.4 mm, the solution C was applied by a gravure method at a rate of a coating thickness of 1 g / m 2 when dried, and dried to form a conductive layer. To form a conductive sheet (c). Temperature 2 of this conductive sheet (c)
The surface resistance at 0 ° C. × 70% humidity was 10 6 / □. Example 1, on the surface of the conductive layer of the conductive sheet (c),
The dispersions D, D1, D2 and D3 were applied and dried in the same manner as in Example 2 so that the film thickness when dried was 0.8 g / m 2. Inventive conductive sheet (C-D1), conductive sheet (C-D2)
And a conductive sheet (C-D3).
【0024】評価:清浄な厚さ0.1mmの銅板を3×
3cmにカットして評価用サンプルとした。一方、前記
導電性シート(イ)、(ロ)、(ハ)、前記比較例及び
実施例で得られたそれぞれの導電性シートを5×5cm
にカットした。上記銅板を上記導電性シ−トの2枚で、
イオンバリヤー層が銅板に面するようにして挟み、湿っ
た布で全体を包み、これをポリエチレン製の袋内に密閉
し、布地の湿気が外部に蒸発しないようにした。袋の上
から1kgの荷重を掛け、70℃×24時間放置した。
その後室温に戻して銅板を取り出し、銅板の面に発生し
た錆を観察した。その結果を下記表2に示す。Evaluation: A clean 0.1 mm thick copper plate was 3 ×
It was cut into 3 cm to obtain a sample for evaluation. On the other hand, each of the conductive sheets (a), (b), and (c), the conductive sheets obtained in the comparative examples and the examples was 5 × 5 cm.
Cut into pieces. The copper plate is made of two sheets of the conductive sheet,
The ion barrier layer was sandwiched so as to face the copper plate, and the whole was wrapped with a damp cloth, which was sealed in a polyethylene bag so that the moisture of the cloth did not evaporate to the outside. A load of 1 kg was applied from above the bag, and the bag was left at 70 ° C. × 24 hours.
Thereafter, the temperature was returned to room temperature, the copper plate was taken out, and rust generated on the surface of the copper plate was observed. The results are shown in Table 2 below.
【0025】 [0025]
【0026】[0026]
【発明の効果】以上の如き本発明によれば、導電剤若し
くは帯電防止剤としてイオン導電剤を使用した場合に
も、電子部品に損傷を与えることがない導電性シートを
提供することができる。According to the present invention as described above, it is possible to provide a conductive sheet which does not damage electronic components even when an ionic conductive agent is used as a conductive agent or an antistatic agent.
【図1】 本発明の導電性シートの一例の断面を図解的
に示す図。FIG. 1 is a diagram schematically showing a cross section of an example of a conductive sheet of the present invention.
【図2】 本発明の導電性シートの他の例の断面を図解
的に示す図。FIG. 2 is a diagram schematically showing a cross section of another example of the conductive sheet of the present invention.
1:基材シート 2:導電層 3:イオンバリヤー層 4:導電性シート 1: base material sheet 2: conductive layer 3: ion barrier layer 4: conductive sheet
Claims (3)
止層が設けられた導電性シートにおいて、上記導電層又
は帯電防止層の表面に無機イオン交換体を含むイオンバ
リヤー層が形成されていることを特徴とする導電性シー
ト。1. A conductive sheet having a conductive layer or an antistatic layer provided on at least one surface, wherein an ion barrier layer containing an inorganic ion exchanger is formed on the surface of the conductive layer or the antistatic layer. A conductive sheet characterized by the above-mentioned.
性シートの少なくとも一方の表面に無機イオン交換体を
含むイオンバリヤー層が形成されていることを特徴とす
る導電性シート。2. An electroconductive sheet, wherein an ion barrier layer containing an inorganic ion exchanger is formed on at least one surface of the electroconductive sheet containing an electroconductive agent and / or an antistatic agent.
の導電剤又は帯電防止剤を含む請求項1又は2に記載の
導電性シート。3. The conductive sheet according to claim 1, wherein the conductive layer or the antistatic layer contains an ion-conductive conductive agent or an antistatic agent.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12685099A JP4283374B2 (en) | 1999-05-07 | 1999-05-07 | Conductive sheet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12685099A JP4283374B2 (en) | 1999-05-07 | 1999-05-07 | Conductive sheet |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000318080A true JP2000318080A (en) | 2000-11-21 |
| JP4283374B2 JP4283374B2 (en) | 2009-06-24 |
Family
ID=14945410
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12685099A Expired - Lifetime JP4283374B2 (en) | 1999-05-07 | 1999-05-07 | Conductive sheet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4283374B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7097900B2 (en) | 2002-06-14 | 2006-08-29 | Denki Kagaku Kogyo Kabushiki Kaisha | Sheet and electronic component packaging container |
| JP2013237481A (en) * | 2012-05-17 | 2013-11-28 | Achilles Corp | Cover tape |
| US9243013B2 (en) | 2008-08-22 | 2016-01-26 | Nippon Shokubai Co., Ltd. | Ionic compound, method for producing the same, and ion-conductive material comprising the same |
-
1999
- 1999-05-07 JP JP12685099A patent/JP4283374B2/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7097900B2 (en) | 2002-06-14 | 2006-08-29 | Denki Kagaku Kogyo Kabushiki Kaisha | Sheet and electronic component packaging container |
| US9243013B2 (en) | 2008-08-22 | 2016-01-26 | Nippon Shokubai Co., Ltd. | Ionic compound, method for producing the same, and ion-conductive material comprising the same |
| JP2013237481A (en) * | 2012-05-17 | 2013-11-28 | Achilles Corp | Cover tape |
Also Published As
| Publication number | Publication date |
|---|---|
| JP4283374B2 (en) | 2009-06-24 |
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