JPH0749626B2 - Method for producing metal-coated fiber - Google Patents
Method for producing metal-coated fiberInfo
- Publication number
- JPH0749626B2 JPH0749626B2 JP13520886A JP13520886A JPH0749626B2 JP H0749626 B2 JPH0749626 B2 JP H0749626B2 JP 13520886 A JP13520886 A JP 13520886A JP 13520886 A JP13520886 A JP 13520886A JP H0749626 B2 JPH0749626 B2 JP H0749626B2
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- metal
- chemical
- resin
- treatment
- 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
- 239000000835 fiber Substances 0.000 title claims description 49
- 229910052751 metal Inorganic materials 0.000 title claims description 36
- 239000002184 metal Substances 0.000 title claims description 36
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000000126 substance Substances 0.000 claims description 32
- 229920005989 resin Polymers 0.000 claims description 24
- 239000011347 resin Substances 0.000 claims description 24
- 238000007747 plating Methods 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 14
- 230000004913 activation Effects 0.000 claims description 7
- 238000007772 electroless plating Methods 0.000 claims description 6
- 230000001235 sensitizing effect Effects 0.000 claims description 4
- 238000000034 method Methods 0.000 description 27
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 13
- 238000007788 roughening Methods 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 7
- 229910052759 nickel Inorganic materials 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000002759 woven fabric Substances 0.000 description 6
- 239000004744 fabric Substances 0.000 description 5
- 229920002994 synthetic fiber Polymers 0.000 description 5
- 239000012209 synthetic fiber Substances 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 206010070834 Sensitisation Diseases 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- -1 polyethylene terephthalate Polymers 0.000 description 4
- 230000008313 sensitization Effects 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 230000008859 change Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 2
- 239000006172 buffering agent Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910000510 noble metal Inorganic materials 0.000 description 2
- 239000003002 pH adjusting agent Substances 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 239000010970 precious metal Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000001119 stannous chloride Substances 0.000 description 2
- 235000011150 stannous chloride Nutrition 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- KWSLGOVYXMQPPX-UHFFFAOYSA-N 5-[3-(trifluoromethyl)phenyl]-2h-tetrazole Chemical compound FC(F)(F)C1=CC=CC(C2=NNN=N2)=C1 KWSLGOVYXMQPPX-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- BIVUUOPIAYRCAP-UHFFFAOYSA-N aminoazanium;chloride Chemical compound Cl.NN BIVUUOPIAYRCAP-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000005672 electromagnetic field Effects 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
Landscapes
- Chemically Coating (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Shielding Devices Or Components To Electric Or Magnetic Fields (AREA)
- Conductive Materials (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は,化学繊維表面に金属メツキを施した繊維の製
造方法に関するものである。Description: TECHNICAL FIELD The present invention relates to a method for producing a fiber in which the surface of a chemical fiber is plated with metal.
(従来技術) 従来,化学繊維に金属被覆を行うためには,真空蒸着
法,スパツタリング法,無電解メツキ法等がある。真空
蒸着法や,スパツタリング法は設備が高価でコスト的に
問題となり,しかも得られたものは密着性が弱く,屈曲
や家庭洗濯1回で剥離を生じてしまう問題があった。こ
れに対して無電解メツキ法は真空蒸着法やスパツタリン
グ法と同様に得られたものは密着性が弱いという問題点
があるとはいうものの,コストが安価で均一な皮膜が得
られる利点に着目して,密着性向上方法の検討が種々行
われている。(Prior Art) Conventionally, there have been a vacuum deposition method, a sputtering method, an electroless plating method, and the like for performing metal coating on a chemical fiber. The vacuum vapor deposition method and the sputtering method have a problem in that the equipment is expensive and the cost is low. Moreover, the obtained one has a weak adhesion, and there is a problem that the bending or the peeling occurs after one home washing. On the other hand, although the electroless plating method has a problem that adhesion obtained by the same method as the vacuum deposition method and the sputtering method has weak adhesion, it is noted that the cost is low and a uniform film can be obtained. Therefore, various studies have been conducted on methods for improving adhesion.
一般に繊維への無電解メツキ処理は,(1)粗表面化処
理,(2)増感処理,(3)活性化処理,(4)無電解
メツキ処理の各工程を順次経て行われている。この中で
上記(1)の粗表面化処理は以降のメツキ工程で付与さ
れる金属メツキの密着性を左右する重要な工程であり,
一般には化学的粗表面化処理と機械的粗表面化処理の2
種類があるが,通常は主に後者の化学的粗表面化処理に
よって実施されている。しかし,上述の方法で得られた
ものもやはりメツキ金属の繊維への密着性が弱く,屈曲
や家庭洗濯1回で剥離を生じてしまい,決して満足でき
るものではなく,メツキ金属の密着性の向上が強く望ま
れているのが現状である。Generally, the electroless plating treatment of the fiber is performed through the steps of (1) roughening treatment, (2) sensitization treatment, (3) activation treatment, and (4) electroless plating treatment. Among them, the roughening treatment of (1) above is an important step that influences the adhesion of metal plating applied in the subsequent plating step,
Generally, there are two types of chemical roughening treatment and mechanical roughening treatment.
There are different types, but usually the latter is mainly carried out by the chemical roughening treatment. However, the one obtained by the above-mentioned method also has a weak adhesion to the fibers of the metal powder, and it is not satisfactory because it is bent or peeled off after one home washing, and the adhesive property of the metal powder is improved. It is the current situation that is strongly desired.
(発明が解決しようとする問題点) 本発明はこのような現状に鑑みて行われたもので,密着
性の良好な金属メツキを施した化学繊維を得ることを目
的とするものである。(Problems to be Solved by the Invention) The present invention has been made in view of the above situation, and an object thereof is to obtain a chemical fiber having a metal plating with good adhesion.
(問題点を解決するための手段) 本発明は上述の目的を達成するために次の構成を有する
ものである。すなわち本発明は化学繊維を粗表面化した
あとその表面に,該繊維と親和性を有しかつ金属塩を含
有する樹脂を付与し,しかる後に増感処理,活性化処
理,化学メッキ処理からなる無電解メッキ処理を施すこ
とを特徴とする金属被覆繊維の製造方法を要旨とするも
のである。(Means for Solving Problems) The present invention has the following configuration in order to achieve the above-mentioned object. That is, in the present invention, after the chemical fiber is roughened, a resin having an affinity for the fiber and containing a metal salt is applied to the surface, and thereafter, sensitizing treatment, activation treatment, and chemical plating treatment are performed. The gist of the present invention is a method for producing a metal-coated fiber, which is characterized by performing electrolytic plating treatment.
以下,本発明を詳細に説明する。Hereinafter, the present invention will be described in detail.
本発明でいう化学繊維とは,ナイロン6やナイロン66で
代表されるポリアミド系合成繊維,ポリエチレンテレフ
タレートで代表されるポリエステル系合成繊維,ポリア
クリロニトリル系合成繊維,ポリビニルアルコール系合
成繊維,トリアセテートで代表される半合成繊維,ビス
コースレーヨンで代表れさる再生繊維等を意味するもの
である。The chemical fibers referred to in the present invention are represented by polyamide synthetic fibers represented by nylon 6 and nylon 66, polyester synthetic fibers represented by polyethylene terephthalate, polyacrylonitrile synthetic fibers, polyvinyl alcohol synthetic fibers, and triacetate. Semi-synthetic fiber, regenerated fiber represented by viscose rayon, etc.
本発明方法においては,上述の化学繊維に織物,編物,
不織布等の布帛の形で粗表面化処理を施す。粗表面化処
理は,糸条の形で行ってもよい。この粗表面化処理には
機械的方法と化学的方法があり,刃物等によって繊維の
表面を粗面化する機械的方法は,繊維の強度を著しく低
下させる危険性があるので注意を要するが,これに対し
化学的方法は,繊維表面層のみを無機薬品溶液で溶出し
て表面粗化を行うものであるから繊維の強度低下が少な
く,従って粗表面化処理は化学的方法の方が望ましい。
この化学的方法にて行う粗表面化処理条件は,化学繊維
の種類に応じて適宜決定すれば良く,例えばポリエステ
ル繊維の場合に,濃度が2〜10%の水酸化ナトリウム水
溶液に温度80〜95℃で数10分浸漬して粗表面化処理を行
うことができる。このように本発明方法では繊維にまず
粗表面化処理を行った後,十分に洗浄し乾燥する。In the method of the present invention, the above-mentioned chemical fibers are woven, knitted,
A roughening treatment is applied in the form of a non-woven fabric. The roughening treatment may be performed in the form of yarn. There are mechanical and chemical methods for this roughening treatment, and the mechanical method of roughening the surface of the fiber with a knife etc. has the risk of significantly reducing the strength of the fiber, but caution is required. On the other hand, in the chemical method, since only the fiber surface layer is eluted with an inorganic chemical solution for surface roughening, the strength of the fiber is not significantly reduced. Therefore, the roughening treatment is preferably a chemical method.
The conditions for the surface roughening treatment performed by this chemical method may be appropriately determined depending on the type of chemical fiber. For example, in the case of polyester fiber, the concentration of sodium hydroxide aqueous solution having a concentration of 2 to 10% is used at a temperature of 80 to 95 ° C. The surface can be roughened by immersing it for several tens of minutes. As described above, in the method of the present invention, the fiber is first roughened, then thoroughly washed and dried.
次に粗表面化された繊維布帛に,布帛を構成する化学繊
維と親和性を有しかつ金属塩を含有する樹脂を付与す
る。ここでいう樹脂とはAl,Ca等のアルカリ土類金属塩,
Cr,Fe,Ni等の遷移金属塩を含有するポリウレタン系樹
脂,アクリル系樹脂,ポリエステル系樹脂,ポリアミド
系樹脂等を意味する。金属塩の使用量は,樹脂重量に対
して0.5〜10%の範囲が好ましい。0.5%未満では,メツ
キすべき金属との親和性に乏しく密着性に対して効果を
発揮できない。他方,10%を超えると樹脂特性の面でも
ろくなる欠点を生じるばかりでなく,密着性の面でも10
%以下と変わらないため不利となる。Next, a resin having affinity with the chemical fibers forming the cloth and containing a metal salt is applied to the roughened fiber cloth. The resin referred to here is Al, Ca or other alkaline earth metal salt,
It means a polyurethane resin, an acrylic resin, a polyester resin, a polyamide resin, etc. containing a transition metal salt such as Cr, Fe, and Ni. The amount of the metal salt used is preferably in the range of 0.5 to 10% based on the weight of the resin. If it is less than 0.5%, the affinity with the metal to be plated is poor and the effect on the adhesion cannot be exerted. On the other hand, if it exceeds 10%, not only does it have the drawback of becoming brittle in terms of resin properties, but also in terms of adhesion.
It is disadvantageous because it does not change below%.
使用する樹脂の選定は化学繊維の種類,樹脂自体の可と
う性をもとに適宜決定すればよい。また,上記金属塩を
含有する樹脂の使用量については,繊維への樹脂の親和
力ならびに金属塩の金属メツキへの親和力の双方から考
えて,繊維重量に対して1〜10%の範囲が望ましく,1%
未満では塩密着性が向上せず,10%を超えると繊維製品
としての特性である風合の柔軟性が損なわれ,更に密着
性についても大きな変化が望めないばかりかコスト面か
ら考えても有利ではない。The resin to be used may be appropriately selected based on the type of chemical fiber and the flexibility of the resin itself. The amount of the resin containing the metal salt used is preferably in the range of 1 to 10% with respect to the weight of the fiber, considering both the affinity of the resin for the fiber and the affinity of the metal salt for the metal plating. 1%
If it is less than 10%, the salt adhesiveness is not improved, and if it exceeds 10%, the flexibility of the texture, which is a characteristic of a textile product, is impaired. Further, a great change in the adhesiveness is not expected, and it is advantageous from the viewpoint of cost. is not.
上述の金属塩を含有する樹脂を付与するためには,その
樹脂溶液に粗表面化された布帛を浸漬し,マングルにて
絞った後温度100〜120℃で乾燥するか,あるいは浸漬後
ただちに乾燥する等の方法により行うことができ,適宜
布帛の型態により決定すれば良い。In order to apply the resin containing the above-mentioned metal salt, the roughened fabric is dipped in the resin solution, squeezed with a mangle and dried at a temperature of 100 to 120 ° C, or immediately after the dipping And the like, and may be appropriately determined depending on the type of cloth.
樹脂と繊維との親和力を高める目的で熱処理を行う場合
には,その処理条件は化学繊維の種類に応じて選定され
るものであるが,一般に温度150〜170℃にて30秒〜60秒
の範囲で熱処理を行うとよい。When heat treatment is performed for the purpose of increasing the affinity between resin and fiber, the treatment conditions are selected according to the type of chemical fiber, but generally, the temperature is 150 to 170 ° C for 30 to 60 seconds. It is advisable to perform heat treatment within the range.
本発明方法では次に増感処理及び活性化処理を行う。こ
の増感処理及び活性化処理の目的は,化学メツキ処理以
前に触媒貴金属を付着させる為の工程であり,この2工
程がメツキの均一性を決定付ける重要な工程である。In the method of the present invention, sensitization treatment and activation treatment are then performed. The purpose of this sensitization treatment and activation treatment is a step for depositing the catalytic noble metal before the chemical plating treatment, and these two steps are important steps for determining the uniformity of the plating.
ここで行う増感処理工程は比較的強い還元剤を繊維表面
に吸着させる工程であり,還元剤としては塩化第一ス
ズ,次亜リン酸,塩化ヒドラジン,ハイドロキノンなど
を使用することができる。続く活性化処理工程では,前
述の処理布を貴金属イオンを含む触媒溶液に浸漬し,繊
維表面に貴金属を析出させて次工程でメツキされる金属
との反応促進を計る。The sensitizing step performed here is a step of adsorbing a relatively strong reducing agent on the fiber surface, and stannous chloride, hypophosphorous acid, hydrazine chloride, hydroquinone or the like can be used as the reducing agent. In the subsequent activation treatment step, the above-mentioned treated cloth is dipped in a catalyst solution containing a precious metal ion to deposit the precious metal on the surface of the fiber to accelerate the reaction with the metal to be plated in the next step.
一般に触媒としては金,銀,白金,パラジウムなどの貴
金属が使用されているが,この中でコスト面および処理
の均一性の面からパラジウムを用いるのが望ましい。前
述の増感処理及び上述の活性化処理の条件については一
般に公知の通常条件で行えばよい。In general, noble metals such as gold, silver, platinum and palladium are used as the catalyst. Among them, it is preferable to use palladium from the viewpoint of cost and uniformity of treatment. Regarding the conditions of the above-mentioned sensitizing process and the above-mentioned activating process, generally known normal conditions may be used.
本発明方法では次に化学メツキ処理を施す。この化学メ
ツキ処理における化学メツキ浴及び処理条件について
は,従来より実施されている公知条件で行えばよい。化
学メツキ浴は金属塩,還元剤,緩衝剤,pH調整剤などで
浴組成されているものである。この中で金属塩としては
銀,銅,ニツケル,コバルト,スズなどの金属塩を用い
ることができるが,メツキ浴の安定性,操作の容易性な
どの点から考えて銅、ニツケルが特に使用しやすい。還
元剤,緩衝剤,pH調整剤については,メツキされる金属
によって決定されるものであり,必要に応じて適宜選定
すればよい。In the method of the present invention, a chemical plating process is then performed. Regarding the chemical plating bath and the processing conditions in this chemical plating treatment, known conditions which have been conventionally practiced may be used. The chemical plating bath is composed of a metal salt, a reducing agent, a buffering agent, a pH adjusting agent and the like. Among these, metal salts such as silver, copper, nickel, cobalt, tin can be used as the metal salt, but copper and nickel are especially used in consideration of stability of the plating bath and ease of operation. Cheap. The reducing agent, the buffering agent, and the pH adjusting agent are determined by the metal to be plated, and may be appropriately selected as needed.
(作用) 本発明の金属被膜繊維は繊維表面と金属膜の界面に,金
属塩を含有しかつ該繊維と親和性を有する樹脂の層を介
在せしめてなる繊維である。従って繊維表面と樹脂層の
界面においては,繊維と樹脂の親和性が強い為該樹脂は
繊維との間に高い密着性を示すとともに,金属膜と樹脂
層の界面においては,該樹脂は樹脂中に有する金属塩が
金属膜との間に強固な密着性を示すようになる。かくし
て本発明による金属被覆化学繊維は金属被膜の繊維への
密着性が飛躍的に向上したものとなる。(Function) The metal-coated fiber of the present invention is a fiber obtained by interposing a resin layer containing a metal salt and having an affinity for the fiber at the interface between the fiber surface and the metal film. Therefore, at the interface between the fiber surface and the resin layer, the resin has a high affinity with the fiber because the affinity between the fiber and the resin is strong, and at the interface between the metal film and the resin layer, the resin is The metal salt contained in the above exhibits strong adhesion to the metal film. Thus, the metal coated chemical fiber according to the present invention has dramatically improved adhesion of the metal coating to the fiber.
(実施例) 次に,本発明方法を実施例により詳細に説明するが,実
施例における密着性の評価については,全自動洗濯機NA
-5580型(松下電器(株)製品)を使用し,液体洗剤ザ
ブ酵素(花王(株)製品)0.5g/lにて温度40℃で10分間
の洗濯を行い,続いて常温で15分間のすすぎを行った
後,脱水,乾燥する1サイクルを洗濯1回とし,これを
5回繰り返し行った後,JIS C-6481にて表面抵抗の測定
を行った。また,これとともに洗濯後の外観変化を視感
で判定し,評価を行った。(Examples) Next, the method of the present invention will be described in detail with reference to Examples. As for the evaluation of adhesion in Examples, a fully automatic washing machine NA
-Using 5580 type (Matsushita Electric Co., Ltd. product), 0.5g / l of liquid detergent Zabu Enzyme (Kao Co., Ltd. product) was washed at a temperature of 40 ° C for 10 minutes, and then at room temperature for 15 minutes. After rinsing, one cycle of dehydration and drying was defined as one wash, and this was repeated 5 times, and then the surface resistance was measured according to JIS C-6481. At the same time, the appearance change after washing was visually judged and evaluated.
実施例1 経糸,緯糸ともポリエチレンテレフタレート繊維75デニ
ール/48フイラメントの原糸で構成された平組織の織物
タフタを用意し,まず精錬処理で脱脂し,次に濃度4%
の水酸化ナトリウム水溶液に温度90℃で30分間浸漬し,
更に濃度2%の塩酸水溶液に常温で10秒間浸漬した後,
流水中で十分に洗浄し,乾燥した。かくして粗表面化さ
れた織物を得た。Example 1 A woven fabric taffeta having a flat structure composed of polyethylene terephthalate fiber 75 denier / 48 filament raw yarn was prepared for both warp and weft, and was first degreased by refining treatment, and then the concentration was 4%.
Immerse it in the sodium hydroxide aqueous solution at 90 ℃ for 30 minutes,
After further immersing in 2% hydrochloric acid aqueous solution at room temperature for 10 seconds,
It was thoroughly washed in running water and dried. Thus, a woven fabric having a roughened surface was obtained.
続いて以下(1)〜(4)の各工程の処理を順次経て,
本発明のニツケルメツキ層を有する金属被覆ポリエステ
ル繊維織物を得た。Then, after sequentially performing the processes of the following steps (1) to (4),
A metal-coated polyester fiber woven fabric having a nickel plating layer of the present invention was obtained.
(1) 樹脂付与工程 下記樹脂処方1の樹脂水溶液に浸漬した後,絞り率50%
のマングルにて絞り,続いて温度100℃にて1分間乾燥
した後,温度170℃で30秒間の熱処理を行った。(1) Resin application step After immersing in the resin aqueous solution of the following resin formulation 1, draw ratio 50%
After squeezing with a mangle, and then drying at a temperature of 100 ° C for 1 minute, heat treatment was performed at a temperature of 170 ° C for 30 seconds.
処方1 ハイドランHW-140 10%sol (大日本インキ(株)製の固型分30%のポリウレタンエ
マルジヨン) 硫酸アルミニウム 0.1%sol (2) 増感処理工程 常温にて塩化第一スズ10g/lの塩酸4%水溶液に5分間
浸漬した後,十分に水洗した。Prescription 1 Hydran HW-140 10% sol (Polyurethane emulsion made by Dainippon Ink and Co., Ltd. with a solid content of 30%) Aluminum sulfate 0.1% sol (2) Sensitization process Stannous chloride 10g / l at room temperature After dipping in 4% aqueous solution of hydrochloric acid for 5 minutes, it was thoroughly washed with water.
(3) 活性化処理工程 常温にて塩化パラジウム0.3g/lの塩酸0.5%水溶液に5
分間浸漬した後十分に水洗した。(3) Activation treatment process At room temperature, add 5 g of palladium chloride 0.3 g / l hydrochloric acid 0.5% aqueous solution.
After soaking for a minute, it was thoroughly washed with water.
(4) 化学メツキ処理工程 温度70℃の下記処方2の水溶液(pH=5)に5分間浸漬
した後,十分に水洗し乾燥した。(4) Chemical plating treatment step After immersion in an aqueous solution (pH = 5) of the following formulation 2 at a temperature of 70 ° C. for 5 minutes, it was thoroughly washed with water and dried.
処方2 硫酸ニツケル 30g/l 次亜リン酸ソーダ 10g/l 酢酸ソーダ 10g/l 得られた本発明のニツケルメツキ織物の性能を測定評価
し,その結果を第1表に示した。Formulation 2 Nickel sulphate 30 g / l Sodium hypophosphite 10 g / l Sodium acetate 10 g / l The performance of the obtained nickel woven fabric of the present invention was measured and evaluated, and the results are shown in Table 1.
本発明方法との比較のため,本実施例において上記
(1)の樹脂付与工程を削除するほかは本実施例と全く
同一の条件で処理を行い,比較用のニツケルメツキ織物
を得た。その性能を測定し併せて第1表に示した。For comparison with the method of the present invention, processing was carried out under exactly the same conditions as in this example except that the resin application step in (1) above was omitted in this example, and a nicknamed woven fabric for comparison was obtained. The performance was measured and is also shown in Table 1.
第1表から明らかなごとく本発明方法で得られたニツケ
ルメツキ織物は,ニツケル金属の密着性に優れているこ
とが認められた。 As is clear from Table 1, it was confirmed that the nickel woven fabric obtained by the method of the present invention was excellent in the adhesion of nickel metal.
(発明の効果) 本発明は化学繊維に無電解メツキを行うに際し,粗表面
化された化学繊維へ予め該繊維と親和性を有しかつ金属
塩を含有する樹脂を付与する点に特徴を有し,かかる本
発明の方法によれば金属メツキの化学繊維への密着性を
飛躍的に向上させることができる。本発明方法で得られ
る金属被覆化学繊維製品は,衣料分野あるいは電磁波シ
ールド分野での用途として極めて有用である。(Effects of the Invention) The present invention is characterized in that, when electroless plating is performed on chemical fibers, a resin having affinity with the fibers and containing a metal salt is previously added to the roughened chemical fibers. According to the method of the present invention, the adhesiveness of the metal powder to the chemical fiber can be dramatically improved. The metal-coated chemical fiber product obtained by the method of the present invention is extremely useful for applications in the field of clothing or electromagnetic field.
───────────────────────────────────────────────────── 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 D06M 15/00 // D06M 101:06 101:16 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display location D06M 15/00 // D06M 101: 06 101: 16
Claims (1)
に,該繊維と親和性を有しかつ金属塩を含有する樹脂を
付与し,しかる後に増感処理,活性化処理,化学メッキ
処理からなる無電解メッキ処理を施すことを特徴とする
金属被覆繊維の製造方法。1. A chemical fiber is surface-roughened, and then a resin having an affinity for the fiber and containing a metal salt is applied to the surface of the chemical fiber. Thereafter, sensitizing treatment, activation treatment, and chemical plating treatment are performed. A method for producing a metal-coated fiber, which comprises performing an electroless plating treatment as described above.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13520886A JPH0749626B2 (en) | 1986-06-10 | 1986-06-10 | Method for producing metal-coated fiber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13520886A JPH0749626B2 (en) | 1986-06-10 | 1986-06-10 | Method for producing metal-coated fiber |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62299567A JPS62299567A (en) | 1987-12-26 |
| JPH0749626B2 true JPH0749626B2 (en) | 1995-05-31 |
Family
ID=15146378
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13520886A Expired - Lifetime JPH0749626B2 (en) | 1986-06-10 | 1986-06-10 | Method for producing metal-coated fiber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0749626B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6068917A (en) * | 1996-03-29 | 2000-05-30 | Ngk Insulators, Ltd. | Composite metallic wire and magnetic head using said composite metal wire |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6703123B1 (en) * | 2000-02-18 | 2004-03-09 | Mitsubishi Materials Corporation | Conductive fiber, manufacturing method therefor, apparatus, and application |
| KR100982019B1 (en) * | 2008-02-05 | 2010-09-13 | 한국기계연구원 | Hollow metal fiber for absorbing electromagnetic waves |
| CN103194891A (en) * | 2013-03-31 | 2013-07-10 | 卜庆革 | Silver-based anti-bacterial and anti-static fibers, production method of fibers, and clothes made from fibers |
-
1986
- 1986-06-10 JP JP13520886A patent/JPH0749626B2/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6068917A (en) * | 1996-03-29 | 2000-05-30 | Ngk Insulators, Ltd. | Composite metallic wire and magnetic head using said composite metal wire |
| US6180890B1 (en) | 1996-03-29 | 2001-01-30 | Ngk Insulators, Ltd. | Composite type magnetic head using composite metallic wire |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62299567A (en) | 1987-12-26 |
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