JPS5824508B2 - Glossy palladium plating bath - Google Patents
Glossy palladium plating bathInfo
- Publication number
- JPS5824508B2 JPS5824508B2 JP6574580A JP6574580A JPS5824508B2 JP S5824508 B2 JPS5824508 B2 JP S5824508B2 JP 6574580 A JP6574580 A JP 6574580A JP 6574580 A JP6574580 A JP 6574580A JP S5824508 B2 JPS5824508 B2 JP S5824508B2
- Authority
- JP
- Japan
- Prior art keywords
- palladium
- plating
- plating bath
- bath
- palladium plating
- 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
Links
Landscapes
- Electroplating And Plating Baths Therefor (AREA)
Description
【発明の詳細な説明】
本発明は光沢のすぐれたパラジウムメッキを可能きする
メッキ浴の組成に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a composition of a plating bath that enables palladium plating with excellent gloss.
パラジウムメッキは耐食性が良く、硬度も高いものかえ
られるので電気関係の用途の他特に装飾用に対しては光
沢がよく変色しにくいことが強く望まれている。Palladium plating has good corrosion resistance and high hardness, so it is strongly desired that it be glossy and resistant to discoloration, especially for decorative purposes in addition to electrical applications.
従来の一般的パラジウムメッキは変色し易く、すぐ特有
の暗色になり見映えが悪く装飾用には不適とされている
。Conventional general palladium plating is prone to discoloration and quickly turns into a characteristic dark color, which makes it look unsightly, making it unsuitable for decorative purposes.
従来の光沢パラジウムメッキ浴はパラジウム源のpH調
整およびパラジウム錯塩安定の目的ないし緩衝剤と(7
てアンモニア水を使用して溶解し、これに各種の光沢剤
を加えた複雑な系で行うことが多かった。Conventional bright palladium plating baths are used for the purpose of adjusting the pH of the palladium source and stabilizing the palladium complex salt, or as a buffering agent (7
This was often done using a complex system in which various types of brighteners were added to the solution using ammonia water.
しかし、こうした系ではメッキ作業の進行につれ陽極板
付近に茶褐色の沈殿物が析出し巻込み電着が生じ、被メ
ッキ体の電着状態が悪化し、特に光沢性、見映えが悪化
する等メッキに悪影響を与える。However, in such a system, as the plating process progresses, brownish precipitates are deposited near the anode plate, resulting in entrained electrodeposition, which deteriorates the electrodeposition condition of the object to be plated, causing deterioration in gloss and appearance, etc. adversely affect.
またアンモニアは特有の強い臭気による作業環境の悪化
をもたらす。Ammonia also causes a deterioration of the working environment due to its unique strong odor.
さらにこの浴は数日間で分解し、浴の安定性が劣るなど
の問題があった。Furthermore, this bath decomposed within a few days, resulting in poor bath stability.
本発明はこうした諸問題を解決する新規なメッキ浴を提
供することを目的とする。The object of the present invention is to provide a new plating bath that solves these problems.
本発明はジクロロジアミンパラジウムをパラジウム換算
量で1〜20 ’if/l、水酸化ナトリウム1〜20
f/7及びサッカリンアルカリ1〜i o o y7
tからなる水性パラジウムメッキ浴を提供する。The present invention uses dichlorodiamine palladium in an amount of 1 to 20 if/l in terms of palladium, and sodium hydroxide in an amount of 1 to 20
f/7 and saccharin alkali 1 to i o o y7
Provided is an aqueous palladium plating bath consisting of t.
パラジウム光沢メッキを行なう場合、一般に光沢剤の選
択が問題となる。When performing palladium bright plating, the selection of brightener is generally a problem.
例えば、特開昭54−67528には多くの化合物が示
されている。For example, many compounds are disclosed in JP-A-54-67528.
こうした有機、無機の各種化合物が単独あるいは複雑な
組合せにより光沢剤として用いられ、それがメッキの光
沢や強度に影響を与えることが知られている。It is known that these various organic and inorganic compounds are used alone or in complex combinations as brighteners, and that they affect the gloss and strength of plating.
従来の系ではこれらにpH調整剤ないしパラジウム溶解
液としてアンモニア水が用いられ、溶液中のパラジウム
は、アンモニア錯塩として溶存しており(例えば特公昭
42−20164)、さらに緩衝剤として各種アンモニ
ウム塩、硫酸塩、リン酸塩、亜硫酸塩などが添加される
ことが一般的である。In conventional systems, ammonia water is used as a pH adjuster or palladium solution, and palladium in the solution is dissolved as an ammonia complex salt (for example, Japanese Patent Publication No. 42-20164), and various ammonium salts, etc. are used as buffering agents. Sulfates, phosphates, sulfites, etc. are commonly added.
また光沢メッキ浴のpl(は従来pI−T8〜12程度
のアルカリ性で行なわれることが多く、いずれもアンモ
ニウムイオンを多量に含む。Furthermore, the bright plating bath (PL) is conventionally often carried out at an alkaline pH of about 8 to 12, and both contain a large amount of ammonium ions.
このアンモニウムイオンはパラジウムのアンモニア錯塩
の安定性を高める重要な要素として位置づけられてきた
。This ammonium ion has been positioned as an important element that increases the stability of palladium ammonia complex salts.
本発明は、こうした複雑なメッキ浴の系に代って、極め
て単純な三成分を必須とする系を使うことにより、すぐ
れた光沢のパラジウムメッキを可能とするパラジウムメ
ッキ浴を実現した。The present invention has realized a palladium plating bath that enables palladium plating with excellent gloss by using an extremely simple system that requires three components in place of such a complicated plating bath system.
即ち本発明のメッキ浴はパラジウム源としてジクロロジ
アミンパラジウムをパラジウム量換算で1〜201/)
(好ましくは5〜10 ?/l )含有し水酸化ナトリ
ウム1〜20 f?/l (好ましくは5〜10 f/
/! )の溶液に溶解した水性メッキ浴でpHは強アル
カリ性であり、好ましくは凡そpH13〜14でメッキ
を行う。That is, the plating bath of the present invention uses dichlorodiamine palladium as a palladium source, in terms of palladium amount of 1 to 201/).
(preferably 5-10?/l) containing 1-20 f? of sodium hydroxide. /l (preferably 5-10 f/
/! ) is dissolved in an aqueous plating bath with a strongly alkaline pH, preferably at approximately pH 13 to 14.
本発明の浴の第1の利点は従来のアンモニアを(パラジ
ウム源に含まれるアンモニアを除いて)一切添加しない
メッキ浴としたことにより、陽極板付近での沈殿の析出
問題が解消されメッキの劣化が防止されることであり、
第2の利点は浴の安定性が向上して長期間安定的な操業
が可能となったこと、さらに第3にアンモニア臭気を大
きく軽減したことである。The first advantage of the bath of the present invention is that the conventional plating bath does not contain any ammonia (except for the ammonia contained in the palladium source), which eliminates the problem of precipitation near the anode plate and deteriorates the plating. is to be prevented;
The second advantage is that the stability of the bath is improved, allowing stable operation over a long period of time, and the third advantage is that the ammonia odor is greatly reduced.
光沢剤としてはサッカリンナトリウム、サッカリンカリ
ウム等のサッカリンアルカリ1〜1001/l(好まし
くは20〜50y7t)を用いることによりさらに第4
の利点としてメッキ層は優れた光沢を有し緻密で耐食性
にすぐれ厚さも5μ以上ないし7μまでクラックなしで
十分に得られることがあげられる。As a brightening agent, a saccharin alkali such as saccharin sodium or saccharin potassium is used in an amount of 1 to 1001/l (preferably 20 to 50 y7t).
The advantages of this are that the plated layer has excellent gloss, is dense, has excellent corrosion resistance, and can be sufficiently thick from 5μ or more to 7μ without cracking.
従来のパラジウムメッキの欠点であった変色の点でも本
発明のパラジウムメッキは良い結果を示し、アンモニア
や亜硫酸ガスの雰囲気中での耐変色性は良好である。The palladium plating of the present invention shows good results in terms of discoloration, which is a drawback of conventional palladium plating, and has good discoloration resistance in an atmosphere of ammonia or sulfur dioxide gas.
また、この浴でメッキしたメッキ物はハンダ濡れ性が良
好である(濡れ角度40〜45勤にの浴によるメッキは
被メッキ体として、銅、真鍮をはじめ金、銀、ロジウム
、コバルト、ニッケルなどに適応でき、アンモニアガス
や亜硫酸ガス。In addition, plated objects plated with this bath have good solder wettability (plating with a bath with a wetting angle of 40 to 45 times can be applied to copper, brass, gold, silver, rhodium, cobalt, nickel, etc.). Can be applied to ammonia gas and sulfur dioxide gas.
等から保護する仕上げメッキとして好適である。It is suitable as a finishing plating to protect from the like.
浴温は30〜60℃とするが、但し、この温度は必ずし
も限定的でなく上限は塩化ビニル製等の装置の耐熱性の
観点から、また下限は処理速度等の観点から一般的に規
定されるものである。The bath temperature is 30 to 60°C, but this temperature is not necessarily limited, and the upper limit is generally specified from the viewpoint of heat resistance of equipment such as vinyl chloride, and the lower limit is generally specified from the viewpoint of processing speed, etc. It is something that
電流密度は凡そ0.5〜1.5A/diが望ましいが、
これも一般的な範囲を示すものである。The current density is preferably approximately 0.5 to 1.5 A/di, but
Again, this is a general range.
但し、電流密度が大きすぎると水素ガスの発生による害
が生ずる危険性がある。However, if the current density is too large, there is a risk that harm may occur due to the generation of hydrogen gas.
一般にはメッキ通電中攪拌を行うことが好ましい。Generally, it is preferable to carry out stirring during plating current application.
以下に本発明の実施例を示す。Examples of the present invention are shown below.
実施例
ジクロロジアミンパラジウム(Pd (NH3’)2C
12)Pd換算量 6 f/1
水酸化ナトリウム 12.51/lサツカ
リンナトリウム 20 f/7O
(C6H4< >N N a
02
pH13
上記浴を温度50℃、電流密度IA/drn′でカソー
ドロッカーで攪拌しながら真鍮板を被メッキ体として2
5分間メッキした。Example dichlorodiamine palladium (Pd (NH3')2C
12) Pd equivalent amount 6 f/1 Sodium hydroxide 12.51/l Saccharin sodium 20 f/7O (C6H4<>N Na 02 pH 13 The above bath was heated at a temperature of 50°C and a current density of IA/drn' with a cathode rocker. 2. While stirring, use a brass plate as the object to be plated.
Plated for 5 minutes.
その結果光沢ある5μ厚の析出物が得られた。As a result, a shiny precipitate with a thickness of 5 μm was obtained.
このパラジウムメッキの耐食性をアンモニア雰囲気中で
24時間曝気して調べたが何らの変色も認められなかっ
た。The corrosion resistance of this palladium plating was examined by aeration in an ammonia atmosphere for 24 hours, but no discoloration was observed.
Claims (1)
1〜20 fI/7.水酸化ナトリウム1〜20 f/
lおよびサッカリンアルカリ1〜100y7tからなる
水性パラジウム電気メッキ浴。1 to 20 fI/7.1 in palladium equivalent amount of dichlorodiamine palladium. Sodium hydroxide 1-20 f/
an aqueous palladium electroplating bath consisting of 1-100y7t of saccharin alkali and 1-100y7t of saccharin alkali.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6574580A JPS5824508B2 (en) | 1980-05-17 | 1980-05-17 | Glossy palladium plating bath |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6574580A JPS5824508B2 (en) | 1980-05-17 | 1980-05-17 | Glossy palladium plating bath |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56163293A JPS56163293A (en) | 1981-12-15 |
JPS5824508B2 true JPS5824508B2 (en) | 1983-05-21 |
Family
ID=13295853
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6574580A Expired JPS5824508B2 (en) | 1980-05-17 | 1980-05-17 | Glossy palladium plating bath |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5824508B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10612149B1 (en) | 2019-09-05 | 2020-04-07 | Chow Sang Sang Jewellery Company Limited | Platinum electrodeposition bath and uses thereof |
-
1980
- 1980-05-17 JP JP6574580A patent/JPS5824508B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS56163293A (en) | 1981-12-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4428802A (en) | Palladium-nickel alloy electroplating and solutions therefor | |
US3677909A (en) | Palladium-nickel alloy plating bath | |
JP6951465B2 (en) | Trivalent chrome plating solution and chrome plating method using this | |
US4911799A (en) | Electrodeposition of palladium films | |
JPH11513078A (en) | Cyanide-free electroplating bath for gold or gold alloy deposition | |
US20040195107A1 (en) | Electrolytic solution for electrochemical deposition gold and its alloys | |
JPS6220279B2 (en) | ||
JP2003530486A (en) | Electrolytic bath for electrochemically depositing palladium or its alloys | |
US4411965A (en) | Process for high speed nickel and gold electroplate system and article having improved corrosion resistance | |
US4184929A (en) | Trivalent chromium plating bath composition and process | |
JPH049875B2 (en) | ||
US3500537A (en) | Method of making palladium coated electrical contacts | |
JPS63203790A (en) | Bright copper-zinc alloy electroplating bath containing no cyanogen compound | |
JPH0270084A (en) | Gold plating bath and gold plating method | |
US4048023A (en) | Electrodeposition of gold-palladium alloys | |
JPS609116B2 (en) | Electrodeposition method for palladium and palladium alloys | |
JPS6250560B2 (en) | ||
US3892638A (en) | Electrolyte and method for electrodepositing rhodium-ruthenium alloys | |
CA1162505A (en) | Process for high speed nickel and gold electroplate system | |
EP0149029A1 (en) | Palladium bath | |
JPS5824508B2 (en) | Glossy palladium plating bath | |
US4615774A (en) | Gold alloy plating bath and process | |
US4634505A (en) | Process and bath for the electrolytic deposition of gold-tin alloy coatings | |
US4411744A (en) | Bath and process for high speed nickel electroplating | |
GB2094836A (en) | A bath for the electrolytic deposition of a palladium-nickel alloy |