JPH0747701B2 - Antistatic material - Google Patents
Antistatic materialInfo
- Publication number
- JPH0747701B2 JPH0747701B2 JP2336588A JP33658890A JPH0747701B2 JP H0747701 B2 JPH0747701 B2 JP H0747701B2 JP 2336588 A JP2336588 A JP 2336588A JP 33658890 A JP33658890 A JP 33658890A JP H0747701 B2 JPH0747701 B2 JP H0747701B2
- Authority
- JP
- Japan
- Prior art keywords
- filler
- weight
- parts
- antistatic
- powder
- 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.)
- Expired - Lifetime
Links
- 239000002216 antistatic agent Substances 0.000 title claims description 23
- 239000011231 conductive filler Substances 0.000 claims description 36
- 239000000945 filler Substances 0.000 claims description 27
- 239000000843 powder Substances 0.000 claims description 24
- 239000000463 material Substances 0.000 claims description 18
- 230000003578 releasing effect Effects 0.000 claims description 16
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 16
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 15
- 239000010985 leather Substances 0.000 claims description 14
- 239000011347 resin Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 14
- 239000002245 particle Substances 0.000 claims description 5
- 235000017166 Bambusa arundinacea Nutrition 0.000 claims description 2
- 235000017491 Bambusa tulda Nutrition 0.000 claims description 2
- 229920002101 Chitin Polymers 0.000 claims description 2
- 108010010803 Gelatin Proteins 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 235000015334 Phyllostachys viridis Nutrition 0.000 claims description 2
- 239000011425 bamboo Substances 0.000 claims description 2
- 239000005018 casein Substances 0.000 claims description 2
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 claims description 2
- 235000021240 caseins Nutrition 0.000 claims description 2
- 229920000159 gelatin Polymers 0.000 claims description 2
- 239000008273 gelatin Substances 0.000 claims description 2
- 235000019322 gelatine Nutrition 0.000 claims description 2
- 235000011852 gelatine desserts Nutrition 0.000 claims description 2
- 241001330002 Bambuseae Species 0.000 claims 1
- 239000003973 paint Substances 0.000 description 36
- 239000011248 coating agent Substances 0.000 description 26
- 238000000576 coating method Methods 0.000 description 26
- 238000010521 absorption reaction Methods 0.000 description 16
- 238000005259 measurement Methods 0.000 description 14
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 11
- 239000002649 leather substitute Substances 0.000 description 11
- 238000003795 desorption Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 229910052782 aluminium Inorganic materials 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 239000002390 adhesive tape Substances 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 244000226021 Anacardium occidentale Species 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000020226 cashew nut Nutrition 0.000 description 1
- NCEXYHBECQHGNR-UHFFFAOYSA-N chembl421 Chemical compound C1=C(O)C(C(=O)O)=CC(N=NC=2C=CC(=CC=2)S(=O)(=O)NC=2N=CC=CC=2)=C1 NCEXYHBECQHGNR-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 239000003273 ketjen black Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Non-Adjustable Resistors (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、適当な電気抵抗値を有する制電性材料に関
し、例えばOA機器用塗料、合成皮革に利用することがで
きる。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an antistatic material having an appropriate electric resistance value, and can be used, for example, as a paint for OA equipment and synthetic leather.
[背景技術] 現在のオフィスにはコンピュータ等のOA機器が多用され
ており、このようなOA機器に静電気障害が発生した場
合、磁気記録類の欠損が生じる虞れがある。そこで、OA
機器用の塗料として、一般の塗料(抵抗値は1014Ω前
後)より抵抗値の低い、制電性(1012Ω以下)又は導電
性(105Ω以下)の塗料が使用されている。従来、この
ような制電性塗料は、一般の塗料100重量部に対して、
球状の導電性フィラーを40〜80重量部添加することによ
り製造されている。また、導電性塗料は、塗料100重量
部に対して、導電性フィラーを100重量部以上添加する
ことにより製造されている。[Background Art] OA equipment such as computers is widely used in the present offices, and when electrostatic damage occurs in such OA equipment, there is a possibility that magnetic recordings may be lost. So OA
As paints for equipment, antistatic (10 12 Ω or less) or conductive (10 5 Ω or less) paints with lower resistance than general paints (resistance value is around 10 14 Ω) are used. Conventionally, such antistatic paint is used for 100 parts by weight of general paint,
It is manufactured by adding 40 to 80 parts by weight of spherical conductive filler. Further, the conductive paint is manufactured by adding 100 parts by weight or more of a conductive filler to 100 parts by weight of the paint.
一方、近年、合成皮革が実用に供されるようになってき
ており、このような合成皮革で制電性を有するものもあ
る。この制電性を有する合成皮革は、例えば合成皮革中
に帯電防止剤を添加したり、導電性基布を使用して製造
されている。On the other hand, in recent years, synthetic leather has come into practical use, and some of such synthetic leathers have antistatic properties. This synthetic leather having antistatic properties is manufactured, for example, by adding an antistatic agent to synthetic leather or using a conductive base cloth.
[発明が解決しようとする課題] 上述した導電性フィラーのみを添加して製造された制電
性(導電性も含む)塗料の場合、球状の導電性フィラー
同士の接触状態を良好にするためには、導電性フィラー
の添加量を増やす必要がある。従って、導電性フィラー
は、銀等の高価な材料より成るものであるため、塗料自
体も高価なものとなっていた。しかも、このような制電
性塗料は、吸放湿性がない上に、手触りが硬いので、感
触が良好ではなかった。[Problems to be Solved by the Invention] In the case of an antistatic (including conductive) coating produced by adding only the above-mentioned conductive filler, in order to improve the contact state between spherical conductive fillers. It is necessary to increase the amount of conductive filler added. Therefore, since the conductive filler is made of an expensive material such as silver, the paint itself is expensive. In addition, such an antistatic paint has no moisture absorption and desorption property, and also has a hard touch, so that the touch is not good.
上述した帯電防止剤を添加した合成皮革では、帯電防止
剤の滲出が生じることがあり、この場合、制電性能が劣
化したり、べたつきが起きたりしていた。In the above-mentioned synthetic leather to which the antistatic agent is added, the antistatic agent may ooze out, in which case the antistatic performance is deteriorated and stickiness occurs.
また、導電性基布を使用した合成皮革では、表皮層で発
生した静電気を中間の多孔質層が邪魔するため、充分な
制電効果が得られなかった。Further, in the synthetic leather using the conductive base cloth, the static electricity generated in the skin layer is obstructed by the intermediate porous layer, so that a sufficient antistatic effect cannot be obtained.
本発明は、制電性に優れ、かつ感触の良好な制電性材料
を提供することを目的とする。An object of the present invention is to provide an antistatic material having excellent antistatic property and having a good feel.
[課題を解決するための手段] 本発明に係る制電性材料は、樹脂基材と、吸放湿性フィ
ラーと、導電性フィラーとが含まれた制電性材料であっ
て、前記樹脂基材100重量部に対して、前記吸放湿性フ
ィラーを5〜35重量部、前記導電性フィラーを5〜35重
量部とし、かつ前記吸放湿性フィラーと導電性フィラー
の和を50重量部以下としたことを特徴とする。[Means for Solving the Problems] The antistatic material according to the present invention is an antistatic material containing a resin base material, a moisture absorbing / releasing filler, and a conductive filler, and the resin base material With respect to 100 parts by weight, the moisture absorptive and desorptive filler is 5 to 35 parts by weight, the conductive filler is 5 to 35 parts by weight, and the sum of the moisture absorptive and desorptive filler and the conductive filler is 50 parts by weight or less. It is characterized by
ここで、制電性材料の制電性とは、抵抗値が1012Ω以
下、好ましくは108Ω以下のことであり、従って105Ω以
下の導電性とされる範囲も含まれる。Here, the antistatic property of the antistatic material means that the resistance value is 10 12 Ω or less, preferably 10 8 Ω or less, and therefore includes a range in which the resistance is 10 5 Ω or less.
前記樹脂基材としては、ウレタン樹脂、その他の樹脂を
任意に使用することができ、膜や層を形成した後に透湿
性を有しているものであることが好ましい。これは、膜
や層中の湿気の移動を容易にして添加された吸放湿性フ
ィラーによる吸放湿性効果を高めるためである。As the resin base material, urethane resin and other resins can be arbitrarily used, and it is preferable that the resin base material has moisture permeability after forming a film or a layer. This is for facilitating the movement of moisture in the film or layer and for enhancing the moisture absorbing / releasing effect of the added moisture absorbing / releasing filler.
この樹脂基材は、制電性材料の具体的用途に応じた組成
となる。例えば、制電性材料を塗料として使用する場合
には、ウレタン樹脂塗料のような樹脂塗料基材であり、
この樹脂塗料基材中には顔料等の塗料として必要な物質
が含まれる。また、皮革塗料として使用する場合にも同
様の組成を有する。更に、合成皮革では、例えば基布上
に形成する乾式ウレタン層又は湿式ウレタン層を介して
形成する乾式ウレタン層の各ウレタン樹脂中に吸放湿性
フィラーと導電性フィラーを含有させる。人工皮革で
は、例えば不織布層に含浸させる湿式ウレタン樹脂中に
吸放湿性フィラーと導電性フィラーを含有させ、またこ
の不織布層上に形成する乾式ウレタン層のウレタン樹脂
中に吸放湿性フィラーと導電性フィラーを含有させる。This resin base material has a composition according to the specific application of the antistatic material. For example, when using an antistatic material as a paint, it is a resin paint base material such as urethane resin paint,
This resin paint base material contains substances necessary for paint such as pigments. Further, it has the same composition when used as a leather paint. Further, in the synthetic leather, for example, a moisture absorbing / releasing filler and a conductive filler are contained in each urethane resin of a dry urethane layer formed on a base cloth or a dry urethane layer formed via a wet urethane layer. In artificial leather, for example, a wet urethane resin impregnated in a nonwoven fabric layer contains a moisture absorbing / releasing filler and a conductive filler, and a dry urethane layer urethane resin formed on this nonwoven fabric layer has a moisture absorbing / releasing filler and conductive filler. Contains a filler.
前記吸放湿性フィラーとしては、皮革粉、シルク粉、キ
チン粉、ゼラチン粉、カゼイン粉、セルロース粉、竹粉
の中から1種又は2種以上を任意に選んだものであっ
て、かつこれらの平均粒径が30μm以下のものを使用す
るのが好ましい。The moisture absorptive and desorptive filler is one or two or more arbitrarily selected from leather powder, silk powder, chitin powder, gelatin powder, casein powder, cellulose powder, and bamboo powder, and these It is preferable to use one having an average particle size of 30 μm or less.
吸放湿性フィラーの平均粒径が30μmを越えると、膜等
の表面が凹凸になってざらつきやすく、しかもスプレー
ガンに目詰まり等が生じて均一な塗布ができなくなる。
より好ましくは、平均粒径が10μm以下のものを使用す
る。If the average particle size of the moisture absorptive and desorptive filler exceeds 30 μm, the surface of the film or the like becomes uneven and is easily roughened, and further, the spray gun is clogged and uniform coating cannot be performed.
More preferably, an average particle size of 10 μm or less is used.
この吸放湿性フィラーの配合量が前記5重量部より少な
い場合には、好ましい感触が得られなくなり、しかも導
電性フィラーの使用量削減の効果も少なくなる。また、
前記35重量部を越える場合には、良好な制電性を示すよ
うになるが、導電性フィラーの添加も加わることによ
り、膜等が脆くなりやすい。好ましくは、吸放湿性フィ
ラーの配合量を8〜25重量部の範囲とする。When the blending amount of the moisture absorbing / releasing filler is less than the above-mentioned 5 parts by weight, the desired feel cannot be obtained, and the effect of reducing the amount of the conductive filler used is reduced. Also,
When the amount exceeds 35 parts by weight, good antistatic property is exhibited, but the addition of the conductive filler tends to make the film and the like brittle. Preferably, the blending amount of the moisture absorbing / releasing filler is in the range of 8 to 25 parts by weight.
前記導電性フィラーとしては、導電性酸化チタンを使用
するのが好ましい。導電性酸化チタンの形状は、針状又
は形状のいずれでよいが、針状が好ましい。針状の場
合、平均短径は0.05〜0.5μm、平均長径は3〜20μm
とするのが好ましい。平均短径と平均長径が上限を越え
ると、短径部が太くなって好ましくない。また、長径が
長くなりすぎると、膜等の表面が凹凸状になってざらつ
き、サンドペーパのような感触になる。しかも、スプレ
ーガンに目詰まり等が生じて均一な塗布ができなくな
る。短径部が細い場合には問題はないが、長径が短い場
合には樹脂基材中において導電性酸化チタン同士の接触
による連続性が悪くなるので好ましくない。It is preferable to use conductive titanium oxide as the conductive filler. The conductive titanium oxide may have a needle shape or a shape, but a needle shape is preferable. In the case of needles, the average short diameter is 0.05 to 0.5 μm and the average long diameter is 3 to 20 μm.
Is preferred. If the average minor axis and the average major axis exceed the upper limits, the minor axis portion becomes thick, which is not preferable. On the other hand, if the major axis becomes too long, the surface of the film or the like becomes uneven, and the surface becomes rough, giving a feeling like sandpaper. In addition, the spray gun is clogged and uniform coating cannot be performed. When the minor axis portion is thin, there is no problem, but when the major axis is short, the continuity due to contact between the conductive titanium oxides in the resin base material is deteriorated, which is not preferable.
また、この導電性酸化チタン以外にも、例えば各種金属
(銅、銀、アルミニウム等)の粉末、繊維状物質(アク
リル繊維等)に酸化スズ、ニッケル、銅、銀等で表面処
理(メッキ等)を施したもの、炭素(ケッチェンブラッ
ク、ファーネスブラック等)に酸化スズ、ニッケル、
銅、銀等で表面処理(メッキ等)を施したものを使用す
ることができる。これらの導電性フィラーは、針状又は
板状とする。好ましくは針状とし、平均短径は0.02〜1.
0μm、平均長径は0.1〜20μmとするのがよい。In addition to the conductive titanium oxide, for example, powder of various metals (copper, silver, aluminum, etc.) and fibrous substances (acrylic fiber, etc.) are surface-treated (plating, etc.) with tin oxide, nickel, copper, silver, etc. Those that have been subjected to, carbon (Ketjen black, furnace black, etc.) tin oxide, nickel,
It is possible to use those that have been surface-treated (plated) with copper, silver or the like. These conductive fillers are needle-shaped or plate-shaped. Preferably needle-like, the average minor axis is 0.02-1.
The average major axis is preferably 0 μm and 0.1 to 20 μm.
この導電性フィラーの配合量が前記5重量部より少ない
場合には、導電性が不十分になる。また、前記35重量部
を越える場合には、吸放湿性フィラーの添加効果が少な
くなる。好ましくは、導電性フィラーの配合量を8〜25
重量部の範囲とする。If the content of the conductive filler is less than 5 parts by weight, the conductivity becomes insufficient. On the other hand, when the amount exceeds 35 parts by weight, the effect of adding the moisture absorptive and desorptive filler decreases. Preferably, the conductive filler content is 8 to 25
The range is parts by weight.
本発明においては、吸放湿性フィラーと導電性フィラー
の各配合量をそれぞれ前記範囲に規定した上で、吸放湿
性フィラーと導電性フィラーの和を50重量部以下とす
る。この和が50重量部を越えると、表面状態がごわごわ
した感じ又はざらざらした感じになると共に、膜等が脆
くなって強度が低下する。In the present invention, the amount of each of the moisture absorptive and desorptive filler and the conductive filler is regulated within the above range, and the sum of the moisture absorptive and desorptive filler and the conductive filler is 50 parts by weight or less. When this sum exceeds 50 parts by weight, the surface condition becomes rough or rough, and the film becomes brittle and the strength is lowered.
本発明に係る制電性材料は、樹脂基材に吸放湿性フィラ
ーと導電性フィラーを添加し、機械的に混合して均一に
分散させることにより得られる。この混合方法として
は、制電性材料の吸湿させないで混合できるものであれ
ば、任意のものを使用できる。The antistatic material according to the present invention is obtained by adding a moisture absorptive and desorptive filler and a conductive filler to a resin base material, mechanically mixing them, and uniformly dispersing them. Any mixing method can be used as long as it can be mixed without allowing the antistatic material to absorb moisture.
本発明に係る制電性材料の具体的用途は、制電性が要求
されるOA機器用塗料、合成皮革、人工皮革等任意であ
る。Specific applications of the antistatic material according to the present invention are arbitrary such as paints for OA equipment, synthetic leather, artificial leather, which require antistatic properties.
[作用] 樹脂基材と導電性フィラーだけで制電性材料を構成しよ
うとした場合、導電性フィラーは最低必要量以上添加し
ないと制電性が得られない。電気抵抗が減少し始める導
電性フィラーの最低必要量添加時に吸放湿性フィラーを
多少添加すると導電性フィラーの最低必要量をやや低減
させることはできるが、吸放湿性フィラーを添加したこ
とにより効果は少ない。しかし、導電性フィラーの添加
量が最低必要量以上になり、導電性フィラーの添加量の
増加と共に、電気抵抗が直線的に減少する範囲において
は、吸放湿性フィラーを添加したことによる効果が最も
有効に現れる。そして、導電性フィラーを添加してもそ
れ以上電気抵抗が減少しない飽和領域においては、吸放
湿性フィラーを添加したことによる効果が得られなくな
る。従って、導電性フィラーの添加によって電気抵抗が
直線的に減少する範囲である添加量が5〜35重量部にお
いて、吸放湿性フィラーを5〜35重量部の範囲で添加す
ることにより10〜104Ω程度の電気抵抗の減少が得られ
ることになる。[Operation] When it is attempted to form the antistatic material only with the resin base material and the conductive filler, the antistatic property cannot be obtained unless the conductive filler is added in a minimum required amount or more. It is possible to slightly reduce the minimum required amount of the conductive filler by adding a little amount of the moisture absorbing and releasing filler at the time of adding the minimum required amount of the conductive filler where the electric resistance starts to decrease, but the effect is not obtained by adding the moisture absorbing and releasing filler. Few. However, in the range where the amount of the conductive filler added becomes the minimum required amount or more and the electrical resistance decreases linearly with the increase of the amount of the conductive filler added, the effect of adding the moisture absorbing / releasing filler is the most effective. Appear effectively. In addition, in the saturated region where the electrical resistance does not further decrease even if the conductive filler is added, the effect of adding the moisture absorbing / releasing filler cannot be obtained. Therefore, in the addition amount of 5 to 35 parts by weight, which is the range in which the electric resistance is linearly reduced by the addition of the conductive filler, 10 to 10 4 by adding the moisture absorbing and releasing filler in the range of 5 to 35 parts by weight. A reduction in electrical resistance of about Ω will be obtained.
これにより、従来の制電性材料と比べて、高価で吸放湿
性のない導電性フィラーの添加量を減らす一方で、安価
で吸放湿性のあるフィラーを添加することにより、良好
な制電性と共に、良好な感触を有する安価な制電性材料
が得られるようになる。As a result, compared with the conventional antistatic material, while reducing the amount of addition of expensive and non-moisture-absorbing conductive filler, by adding inexpensive and hygroscopic filler, good antistatic property At the same time, an inexpensive antistatic material having a good feel can be obtained.
[実施例] 実施例1 樹脂基材として二液ウレタン塗料を使用し、この二液ウ
レタン塗料100重量部に対して、吸放湿性フィラーとし
て皮革粉を24重量部及び導電性フィラーとして針状酸化
チタンを8重量部に加えて機械的に混合し、これらを均
一に分散させて本実施例に係る制電性材料としての制電
性塗料を得た。[Examples] Example 1 A two-component urethane paint was used as a resin base material, and 100 parts by weight of this two-component urethane paint, 24 parts by weight of leather powder as a moisture absorbing / releasing filler and needle-like oxidation as a conductive filler were used. Titanium was added to 8 parts by weight and mechanically mixed, and these were uniformly dispersed to obtain an antistatic coating as an antistatic material according to this example.
本実施例において使用した二液ウレタン塗料は、セノソ
フト〔商品名、カシュー(株)製〕であり、主剤である
セノソフト−A液が80重量部、硬化剤であるセノソフト
−B液が16重量部及び硬化促進剤が4重量部含まれたも
のである。The two-component urethane paint used in this example was Senosoft [trade name, manufactured by Cashew Co., Ltd.], and 80 parts by weight of the main component Senosoft-A liquid and 16 parts by weight of the curing agent Senosoft-B liquid were used. And 4 parts by weight of a curing accelerator.
また、使用した皮革粉は、平均粒径5μmのものであ
る。The leather powder used has an average particle size of 5 μm.
使用した針状導電性酸化チタンは、FT2000〔商品名、石
原産業(株)製〕である。The needle-shaped conductive titanium oxide used is FT2000 [trade name, manufactured by Ishihara Sangyo Co., Ltd.].
次に、この制電性塗料に希釈溶剤であるカシューストロ
ン#2240シンナー〔商品名、カシュー(株)製〕を加え
て希釈した塗料をスプレーガン〔岩田ワイダ71(商品
名)、岩田塗装機工業(株)製〕を使用してABS板に乾
燥時の塗膜厚さが50μmとなるように塗布した。塗布
後、60℃で、40分間乾燥させた。Next, this antistatic paint was diluted with a diluent solvent, Cashew Stron # 2240 thinner (trade name, manufactured by Cashew Co., Ltd.), and the paint was diluted with a spray gun [Iwata Wyder 71 (trade name), Iwata Coating Machine Industry Co., Ltd. Co., Ltd.] was applied to an ABS plate so that the thickness of the coating film when dried was 50 μm. After coating, it was dried at 60 ° C. for 40 minutes.
次に、形成された制電性塗料の塗膜に対して、下記のよ
うにして表面の感触を評価し、また表面固有抵抗と吸放
湿特性を測定した。その結果を表−1に示す。なお、評
価と測定は、いずれも23℃、50%RH(相対湿度)の室内
で行った。Next, with respect to the formed coating film of the antistatic paint, the feel of the surface was evaluated as described below, and the surface specific resistance and the moisture absorption / release property were measured. The results are shown in Table-1. In addition, both evaluation and measurement were performed in a room at 23 ° C. and 50% RH (relative humidity).
表面の感触の評価方法 官能検査の1種である振り分け法に従い、10人の検査員
の塗膜の表面を触ってもらい、ドライタッチを○、非ド
ライタッチを×として評価する。その結果、8人以上の
検査員の評価が一致している場合を○又は×とし、7〜
5人の検査員が評価が一致している場合を△とする。Evaluation method of surface feel In accordance with the distribution method, which is one of the sensory tests, 10 inspectors touch the surface of the coating film, and dry touch is evaluated as ○ and non-dry touch is evaluated as ×. As a result, if the evaluations of 8 or more inspectors are in agreement, it is designated as ○ or ×, and 7 to
The case where the five inspectors agree on the evaluation is Δ.
表面固有抵抗の測定方法 測定装置〔ヒューレットパッカード(株)製、測定用セ
ル:16008A、計測部:4329A〕を使用して表面固有抵抗を
測定する。Measuring method of surface resistivity The surface resistivity is measured using a measuring device [manufactured by Hewlett Packard Co., measuring cell: 16008A, measuring unit: 4329A].
吸放湿特性の測定方法 この吸放湿特性の測定方法は、出光法に基づくものであ
り、吸湿性と放湿性と表裏面を有するフィルム状又はシ
ート状の合成皮革等の表面からの吸湿、放湿速度の測定
方法について規定する。Method for measuring moisture absorption and desorption characteristics This method for measuring moisture absorption and desorption characteristics is based on the light output method, moisture absorption from the surface of a film-like or sheet-like synthetic leather having hygroscopicity and hygroscopicity and front and back surfaces, The method for measuring the moisture release rate is specified.
先ず、第1図に示すように、23℃、50%RH中に24時間放
置して状態調節したオリジナルサンプルより切り出した
(又は打ち抜いた)一辺130mmの正方形のサンプル11を
吸湿度測定用及び放湿度測定用としてそれぞれ1個用意
する。そして、吸湿度測定用サンプル11は、23℃、30%
RHの恒温恒湿槽中に24時間放置して状態調節しておく。
一方、放湿度測定用サンプル11は、23℃、80%RHの恒温
恒湿槽(又は同等の雰囲気の硫酸アンモニウム飽和溶液
を入れた容器)中に24時間放置して状態調節しておく。First, as shown in FIG. 1, a square sample 11 with a side of 130 mm cut out (or punched out) from an original sample that had been conditioned for 24 hours at 23 ° C. and 50% RH for 24 hours was used for moisture absorption measurement and release. Prepare one each for humidity measurement. And the sample 11 for moisture absorption measurement is at 23 ° C, 30%
Leave it in the RH constant temperature and humidity chamber for 24 hours to adjust the condition.
On the other hand, the humidity release sample 11 is left in a constant temperature and humidity chamber at 23 ° C. and 80% RH (or a container containing a saturated solution of ammonium sulfate in the same atmosphere) for 24 hours for conditioning.
次に、一辺130mmの正方形のアルミニウム板12を2枚用
意し、各アルミニウム板12の周囲に幅15mmの両面粘着テ
ープ13を貼り付けた後、このアルミニウム板12に重なる
ようにして両面粘着テープ13に放湿度測定用サンプル11
を貼り付ける。この後、幅15mmのビニルテープ14で周囲
をシールする。Next, prepare two square aluminum plates 12 each having a side of 130 mm, attach a double-sided adhesive tape 13 having a width of 15 mm to the periphery of each aluminum plate 12, and then overlap the aluminum plates 12 so that the double-sided adhesive tape 13 Sample for moisture release measurement 11
Paste. Then, the periphery is sealed with a vinyl tape 14 having a width of 15 mm.
次に、吸湿度測定用サンプル11は、23℃、80%RHの恒温
恒湿槽(又は同等の雰囲気の硫酸アンモニウム飽和溶液
を入れた容器)中に所定時間放置する。一方、放湿度測
定用サンプル11は、23℃、30%RHの恒温恒湿槽中に所定
時間放置する。Next, the moisture absorption measurement sample 11 is left for a predetermined time in a constant temperature and humidity chamber at 23 ° C. and 80% RH (or a container containing a saturated ammonium sulfate solution in an equivalent atmosphere). On the other hand, the humidity release measurement sample 11 is left for a predetermined time in a constant temperature and humidity chamber at 23 ° C. and 30% RH.
次に、各測定時間毎に各サンプル11を恒温恒湿槽から取
り出して1分間経過直後の重量(アルミニウム板12等も
含む)を天秤で1mgまで測定し、記録する。この天秤
は、1mg感度で300g以上の測定可能重量を有するもので
ある。この後、直ちにサンプル11を元の恒温恒湿槽に戻
す。所定の測定時とは、測定開始から20分、40分、60
分、90分、120分及び180分の各経過後である。Next, each sample 11 is taken out from the constant temperature and humidity chamber at each measurement time, and the weight (including the aluminum plate 12 etc.) immediately after 1 minute is measured up to 1 mg by a balance and recorded. This balance has a measurable weight of 300 g or more with a 1 mg sensitivity. Immediately thereafter, the sample 11 is returned to the original constant temperature and humidity chamber. 20 minutes, 40 minutes, 60 minutes from the start of measurement
After each of minutes, 90 minutes, 120 minutes and 180 minutes.
次に、これらの測定結果より次のようにして各測定時間
毎の1m2当たりの吸湿、放湿速度Vg/m2を求める。Next, from these measurement results, the moisture absorption / desorption rate Vg / m 2 per 1 m 2 at each measurement time is obtained as follows.
V=〔(W1−W0)/103〕×〔104/S〕 ここで、W1は各測定時間毎のサンプル11の重量(アルミ
ニウム板12等も含む)、W0はサンプル11の乾燥又は湿潤
状態の基準重量、Sはサンプル11の露出表面積(約100c
m2)である。なお、この測定の際、ビニルテープ14で押
さえられた部分での吸放湿はないものとする。V = [(W 1 −W 0 ) / 10 3 ] × [10 4 / S] where W 1 is the weight of the sample 11 (including the aluminum plate 12 etc.) at each measurement time, and W 0 is the sample 11 Dry or wet basis weight, S is the exposed surface area of sample 11 (about 100c
m 2 ). In this measurement, it is assumed that the portion held by the vinyl tape 14 does not absorb or release moisture.
表の吸放湿特性で、○は測定開始から60分後の吸放湿速
度が1g/m2以上、△は1〜0.5g/m2、×は0.5g/m2以下を
示す。In Hygroscopic properties tables, ○ is moisture-absorbing and desorbing rates of 60 minutes after the start of measurement is 1 g / m 2 or more, △ is 1~0.5g / m 2, × indicates a 0.5 g / m 2 or less.
実施例2〜5 上記実施例1と同様に、実施例2〜5についても、各実
施例に係る制電性塗料を使用して塗膜を形成した後、表
面の感触を評価し、また表面固有抵抗と吸放湿特性を測
定した。その結果を表−1に示す。Examples 2 to 5 Similarly to the above Example 1, also in Examples 2 to 5, after forming a coating film using the antistatic paint according to each Example, the feel of the surface was evaluated, and the surface was also evaluated. The specific resistance and moisture absorption / release characteristics were measured. The results are shown in Table-1.
但し、二液ウレタン塗料に混合した皮革粉の割合及び導
電性フィラーとして使用した針状導電性酸化チタン又は
球状導電性酸化チタンの混合割合は表−1に示すように
異ならせた。なお、使用した球状酸化チタンは、ET500W
〔商品名、石原産業(株)製〕である。However, the proportion of the leather powder mixed in the two-component urethane paint and the proportion of the needle-shaped conductive titanium oxide or spherical conductive titanium oxide used as the conductive filler were varied as shown in Table 1. The spherical titanium oxide used was ET500W.
[Product name, manufactured by Ishihara Sangyo Co., Ltd.].
比較例1〜6 上記実施例と同様に、各比較例に係る塗料を使用して塗
膜を形成した後、表面の感触を評価し、また表面固有抵
抗と吸放湿特性を測定した。その結果を表−1に示す。Comparative Examples 1 to 6 After forming coating films using the coating materials according to each Comparative Example, the surface feel was evaluated, and the surface specific resistance and moisture absorption / desorption characteristics were measured as in the above Examples. The results are shown in Table-1.
但し、比較例1では二液ウレタン塗料のみの塗料、比較
例2では二液ウレタン塗料に皮革粉のみを添加した塗
料、比較例3〜5では二液ウレタン塗料に導電性酸化チ
タンのみを添加した塗料、比較例6では二液ウレタン塗
料に皮革粉と導電性酸化チタンを添加した塗料を使用し
た。比較例で使用した塗料中の皮革粉の混合割合及び導
電性酸化チタンの種類と混合割合も表−1に示す。However, in Comparative Example 1, a paint containing only a two-component urethane paint, in Comparative Example 2 a paint containing only leather powder added to a two-component urethane paint, and in Comparative Examples 3 to 5, only conductive titanium oxide was added to a two-component urethane paint. Paint, in Comparative Example 6, a two-component urethane paint containing leather powder and conductive titanium oxide was used. Table 1 also shows the mixing ratio of the leather powder and the type and mixing ratio of the conductive titanium oxide in the paint used in the comparative example.
表−1より、実施例1〜5に係る塗膜は、二液ウレタン
塗料100重量部に対して、皮革粉が8〜24重量部及び導
電性酸化チタンが8〜24重量部含まれた制電性塗料を使
用して形成されたものであるため、いずれの塗膜も表面
の感触と吸放湿特性が良好であることがわかる。また、
いずれの塗膜も表面固有抵抗が、5×109Ω以下であ
り、好ましい制電性が得られた。 From Table-1, the coating films according to Examples 1 to 5 were coated with 8 to 24 parts by weight of leather powder and 8 to 24 parts by weight of conductive titanium oxide per 100 parts by weight of the two-component urethane paint. It can be seen that all the coating films have good surface feel and good moisture absorption and desorption characteristics because they were formed using an electro-conductive paint. Also,
The surface resistivity of each coating film was 5 × 10 9 Ω or less, and favorable antistatic property was obtained.
これに対して、比較例1に係る塗膜は、皮革粉も酸化チ
タンも含まれていない塗料を使用して形成されたもので
あるため、表面の感触と吸放湿特性が不良であることが
わかる。また、塗膜は表面固有抵抗が、5×1014Ωであ
り、制電性が得られなかった。On the other hand, since the coating film according to Comparative Example 1 was formed by using a paint containing neither leather powder nor titanium oxide, the surface feel and the moisture absorption / desorption property are poor. I understand. Further, the coating film had a surface specific resistance of 5 × 10 14 Ω and could not obtain antistatic property.
また、比較例2に係る塗膜は、皮革粉のみを添加した塗
料を使用して形成されたものであるため、表面の感触と
吸放湿特性は良好であるが、塗膜の表面固有抵抗が2×
1012Ωであり、好ましい制電性が得られなかった。Further, since the coating film according to Comparative Example 2 was formed by using the coating material to which only the leather powder was added, the surface feel and the moisture absorbing / releasing property are good, but the surface specific resistance of the coating film. Is 2 ×
It was 10 12 Ω, and favorable antistatic property was not obtained.
比較例3〜5に係る塗膜は、導電性酸化チタンのみを添
加した塗料を使用して形成されたものであるため、表面
の感触と吸放湿特性及び表面固有抵抗の少なくとも1つ
に問題があることがわかる。Since the coating films according to Comparative Examples 3 to 5 are formed by using the coating material to which only conductive titanium oxide is added, there is a problem in at least one of the feel of the surface, the moisture absorption / release characteristics, and the surface resistivity. You can see that there is.
比較例6に係る塗膜は、皮革粉も導電性酸化チタンも含
まれた塗料を使用して形成されたものであるが、皮革粉
の混合割合が40重量部と本発明に係る上限(35重量部)
を越えているため、表面の感触と吸放湿特性及び表面固
有抵抗に問題はなくても、塗料の粘度が上がりすぎ、ま
た塗膜が非常に脆くなって実用上問題があった。The coating film according to Comparative Example 6 was formed using a coating material containing both leather powder and conductive titanium oxide, but the mixing ratio of the leather powder was 40 parts by weight and the upper limit according to the present invention (35 Parts by weight)
Therefore, even though there is no problem in the feel of the surface, moisture absorption / release characteristics and surface resistivity, the viscosity of the coating is too high, and the coating film becomes very brittle, which is a problem in practical use.
[発明の効果] 本発明によれば、制電性に優れ、かつ感触の良好な制電
性材料が得られる。[Effects of the Invention] According to the present invention, an antistatic material having excellent antistatic property and good touch can be obtained.
第1図は吸放湿特性の測定方法で使用するサンプルの作
り方を示す斜視図である。 11……サンプル、12……アルミニウム板。FIG. 1 is a perspective view showing how to prepare a sample used in the method for measuring the moisture absorption / desorption characteristics. 11 …… Sample, 12 …… Aluminum plate.
Claims (3)
フィラーとが含まれた制電性材料であって、 前記樹脂基材100重量部に対して、前記吸放湿性フィラ
ーを5〜35重量部、前記導電性フィラー5〜35重量部と
し、かつ前記吸放湿性フィラーと導電性フィラーの和を
50重量部以下としたことを特徴とする制電性材料。1. An antistatic material containing a resin base material, a moisture absorptive and desorptive filler, and a conductive filler, wherein 5 parts of the moisture absorptive and desorptive filler is added to 100 parts by weight of the resin base material. ~ 35 parts by weight, the conductive filler 5 ~ 35 parts by weight, and the sum of the moisture absorbing and releasing filler and the conductive filler
An antistatic material characterized by being 50 parts by weight or less.
以下の皮革粉、シルク粉、キチン粉、ゼラチン粉、カゼ
イン粉、セルロース粉、竹粉の中から任意に選ばれたも
のとしたことを特徴とする第1請求項記載の制電性材
料。2. The moisture absorptive and desorptive filler has an average particle diameter of 30 μm.
The antistatic material according to claim 1, which is arbitrarily selected from the following leather powder, silk powder, chitin powder, gelatin powder, casein powder, cellulose powder, and bamboo powder.
したことを特徴とする第1請求項又は第2請求項記載の
制電性材料。3. The antistatic material according to claim 1 or 2, wherein the conductive filler is conductive titanium oxide.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2336588A JPH0747701B2 (en) | 1990-11-30 | 1990-11-30 | Antistatic material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2336588A JPH0747701B2 (en) | 1990-11-30 | 1990-11-30 | Antistatic material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH04202482A JPH04202482A (en) | 1992-07-23 |
| JPH0747701B2 true JPH0747701B2 (en) | 1995-05-24 |
Family
ID=18300707
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2336588A Expired - Lifetime JPH0747701B2 (en) | 1990-11-30 | 1990-11-30 | Antistatic material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0747701B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5656174B2 (en) * | 2013-03-07 | 2015-01-21 | 国立大学法人九州工業大学 | Antistatic agent for polymer composite material and antistatic member |
-
1990
- 1990-11-30 JP JP2336588A patent/JPH0747701B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH04202482A (en) | 1992-07-23 |
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