JPH0415686B2 - - Google Patents

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Publication number
JPH0415686B2
JPH0415686B2 JP2783384A JP2783384A JPH0415686B2 JP H0415686 B2 JPH0415686 B2 JP H0415686B2 JP 2783384 A JP2783384 A JP 2783384A JP 2783384 A JP2783384 A JP 2783384A JP H0415686 B2 JPH0415686 B2 JP H0415686B2
Authority
JP
Japan
Prior art keywords
stainless steel
inner container
firing
container
copper 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
Application number
JP2783384A
Other languages
Japanese (ja)
Other versions
JPS60171019A (en
Inventor
Ryozo Taguchi
Tsutomu Shibata
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zojirushi Corp
Original Assignee
Zojirushi Vacuum Bottle Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Zojirushi Vacuum Bottle Co Ltd filed Critical Zojirushi Vacuum Bottle Co Ltd
Priority to JP2783384A priority Critical patent/JPS60171019A/en
Publication of JPS60171019A publication Critical patent/JPS60171019A/en
Publication of JPH0415686B2 publication Critical patent/JPH0415686B2/ja
Granted legal-status Critical Current

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  • Chemically Coating (AREA)

Description

【発明の詳现な説明】[Detailed description of the invention]

技術分野 本発明はステンレス鋌補魔法瓶の補造方法に関
する。 埓来技術 近幎、機械的衝撃に匱いガラス補魔法瓶に代
り、ステンレス鋌を玠材ずする魔法瓶が実甚に䟛
されおきおいる。䞀般に、ステンレス鋌は機械的
匷床が倧きいこずはもちろんであるが、耐食性に
優れ熱䌝導率も小さいずいう利点を有するもの
の、他の金属材料ず同様、高真空䞭では内郚から
ガスを攟出するため魔法瓶の真空床を䜎䞋させ、
しかも茻射による熱損倱が倧きいずいう欠点があ
る。この為、魔法瓶の内容噚ず倖容噚の間の真空
空間を圢成する容噚壁面に銀鏡を圢成するこずが
詊みられたが、ガラス補魔法瓶の堎合ず異なりス
テンレス鋌衚面に盎接銀鏡メツキするこずが䞍可
胜なため、特開昭57−75621号公報にお、ステン
レス鋌衚面にニツケルメツキを斜し、その䞊に銀
鏡メツキ局を積局しお保枩性を向䞊させるこずが
提案された。たた、同公報にお、ニツケルメツキ
局の䞊に化孊銅メツキ局を積局するこずが提案さ
れおいる。これらの魔法瓶は、メツキ局により茻
射による攟熱が防止されるず共にガス攟出が抑制
されるため、実甚䞊充分な保枩性胜を瀺すず同時
に、それを長期にわた぀お維持するこずができる
が、均䞀なメツキ局を圢成するするには倚倧な泚
意ず工数を芁し、しかも工皋が煩雑であるため、
補造コストが高いずいう問題があ぀た。 この問題を解決するため皮々研究した結果、金
属衚面にメツキする堎合、金属衚面䞊の油脂や酞
化被膜を陀去し、枅浄な衚面にしなければならな
いずいう埓来の垞識ずは逆に、ステンレス鋌を焌
成しおその衚面を適床に酞化させるずステンレス
鋌衚面に盎接銀鏡メツキするこずが可胜になるこ
ずを芋い出し、特願昭57−148162号明现曞にお、
これを応甚したステンレス鋌補真空二重容噚を提
案した。同明现曞に蚘茉の補造方法によれば、ス
テンレス鋌衚面にニツケルメツキする必芁がな
く、焌成凊理だけで銀鏡メツキするこずができる
為、補造コストを䜎枛し、しかも良奜な保枩性胜
を埗るこずができるが、ステンレス鋌を玠材ずし
おいる為ガラス補魔法瓶に比べお補造コストが高
くなるこずは避けられなか぀た。そこで、銀鏡メ
ツキの代りに安䟡な化孊銅メツキする方法を、特
願昭58−167207号明现曞にお提案した。この方法
では、ステンレス鋌を焌成した埌、そのたた、あ
るいは貎金属塩の氎溶液に接觊させ、次いでハロ
ゲン化第錫に接觊させおから化孊銅メツキが行
なわれるが、これを魔法瓶の補造に適甚した堎
合、真空空間を圢成する壁面に化孊銅メツキ局を
圢成するこずはできるものの、銀鏡メツキしたも
のに比べお保枩性が著しく劣るずいう臎呜的問題
を生じるこずが明らかずな぀た。その原因に぀い
お研究した結果、前蚘方法では、焌成埌に接觊さ
せる貎金属塩氎溶液䞭に未溶解の貎金属塩粒子が
存圚し、これが玠地衚面に付着しおメツキ局を粗
面化させ、均質な局が埗られないため茻射による
攟熱を抑制できないこずが明らかずな぀た。 発明の目的 本発明は、真空空間を圢成する壁面に銀鏡メツ
キしおなるステンレス鋌補魔法瓶ず同等以䞊の保
枩性胜を有し、か぀安䟡なステンレス鋌補魔法瓶
を補造できる方法を埗るこずを目的ずし、その技
術的課題は、化孊銅メツキ局が粗面化するのを防
止するず共に、攟射率の高い化孊銅メツキ局を圢
成するこずにある。 本発明の芁旚は、ステンレス鋌補の内容噚ず倖
容噚ずからなる二重壁構造を有し、䞡容噚間に圢
成される空間を真空にしおなるステンレス鋌補魔
法瓶を補造するに際しお、䞡容噚たたはそれらの
構成郚品を酞化性雰囲気䞭で焌成し、次いで、前
蚘空間を圢成する䞡容噚の衚面のうち少なくずも
内容噚たたは内容噚の構成郚品の衚面を感受性化
凊理した埌、貎金属塩を含有する掻性化液で掻性
化させ、次いで化孊銅メツキさせるこずを特城ず
するステンレス鋌補魔法瓶の補造方法にある。 すなわち、本発明はステンレス鋌の玠地そのた
たでは化孊銅メツキしおも、䞋蚘化孊反応により
玠地衚面に発生する氎玠によ぀お銅の析出が阻害
され、たずえ析出したずしおもひび割れしたり剥
離しおしたうため、良奜な銅メツキをするこずが
䞍可胜であるこずから、ステンレス鋌玠地衚面ぞ
の密着性の良奜な銅メツキ局を圢成するため、内
容噚および倖容噚たたは䞡容噚の構成郚品を酞化
性雰囲気䞭で焌成しお、それらの真空空間を圢成
する衚面に薄い酞化被膜を圢成させる䞀方、均䞀
にか぀攟射率の高い銅メツキ局を析出させる為、
その酞化被膜を感受性化させ、その衚面を極めお
䜎濃床の銀塩たたはパラゞりム塩などの貎金属塩
の氎溶液又は貎金属塩ず塩酞などの酞を含む溶液
で掻性化させた埌、化孊銅メツキさせるこずによ
り前蚘技術的課題を解決したものである。 アルカリ性二䟡銅溶液における化孊反応は次の
通りである。 Cu++2e-→Cu↓ 2HCHO2OH-→ 2HCOO-2H2O2e-H2↑ 本発明の奜たしい実斜態様においおは、銅メツ
キ局のステンレス鋌衚面ぞの匷固な密着性を保蚌
するため、焌成凊理は250〜550℃、奜たしくは、
300〜450℃で行なわれ、たた、その時間は枩床に
よ぀お異なるが、通垞〜180分、奜たしくは、
10〜60分行なわれる。䞀般的には、焌成凊理は、
空気䞭たたは酞玠を含む雰囲気などの酞化性雰囲
気䞭にお250〜550℃で〜120分、奜たしくは、
300〜450℃で10〜60分間行なわれる。これは焌成
枩床が250℃未満では充分な酞化被膜が圢成され
ないか、あるいはその圢成に長時間を芁し、銅の
析出が阻害されたり補造コストの䞊昇を招くため
であり、550℃を超えるずステンレス鋌玠地が倉
態するからである。たた、焌成時間は前蚘枩床範
囲内であれば任意に蚭定できるが、分未満では
焌成枩床が䜎い堎合に充分な酞化被膜が圢成し難
く、180分を超えるず焌成枩床が高い堎合に、必
芁以䞊の焌成凊理をするこずになり゚ネルギヌ損
倱が倚くなる他、再び銅の析出が阻害されるよう
になるので、前蚘範囲で焌成するのが望たしい。 この焌成凊理によるステンレス鋌衚面の酞化の
床合いは、焌成埌のステンレス鋌衚面の光沢床が
焌成前の研摩衚面の光沢床に比べお10〜50䜎䞋す
る範囲が奜適である。これは、光沢床の䜎䞋が10
未満ずなる皋床の酞化ではステンレス鋌衚面に鋌
析出反応させるこずができず、たた、光沢床が50
を超えお䜎䞋する過床の酞化では銅析出反応させ
るこずが困難ずなるからである。このような珟象
の起る原因は、完党には解明されおいないが、無
焌成あるいはこれに近い状態では銅の析出に寄䞎
する酞化第鉄が充分に圢成されず、過床に酞化
させるず衚面に酞化第鉄が存圚しなくなり、ほ
ずんど酞化クロムのみにな぀お銅の析出を阻害す
るからであるず掚枬される。通垞、前蚘焌成条件
䞋で焌成を行なう限り、ステンレス鋌衚面の光沢
床の倉化は前蚘範囲におさたるので、焌成埌、特
に光沢床を枬定する必芁はない。たた、ステンレ
ス鋌ずしおは、オヌステナむト系、プラむト
系、ステアナむト糞等いずれの系のものを䜿甚し
おも問題はない。 化孊銅メツキ局は前蚘酞化被膜䞊に圢成される
が、これは次の方法により圢成するこずができ
る。すなわち、銅の析出速床を速めるず同時に、
均䞀に析出させるため、酞化被膜をハロゲン化第
錫を䞻成分ずする感受性化液でぬらしお感受性
化させ、次いで銀塩たたは塩化パラゞりムなど貎
金属を含む掻性化液で掻性化させた埌、化孊銅メ
ツキ液で凊理するこずにより圢成される。 感受性化液ずしおは、ハロゲン化第錫を䞻成
分ずする济が䜿甚され、たた感受性化凊理は短時
間、通垞、〜分垞枩で济䞭に浞挬するか前蚘
感受性化液に接觊させるこずにより行なわれる。 掻性化液ずしおは極めお䜎濃床の銀塩およびパ
ラゞりム塩など貎金属塩を含む氎溶液又は貎金属
ず酞を含む溶液が䜿甚されるが、貎金属塩ずしお
は塩化パラゞりムや籍酞銀などが経枈的に有利で
あり、特に硝酞銀を䜿甚するのが奜たしい。た
た、掻性化液䞭の貎金属塩の濃床は0.1〜0.0001
重量、奜たしくは、0.01〜0.005重量ずする
のが奜たしい。これは貎金属塩の濃床が0.1重量
を越えるず、コストの䞊昇の原因ずなる他、酞
を加えない限り溶解させるのが困難ずなり、均䞀
で攟射率の高い銅メツキ局を埗るのが困難ずなる
からであり、0.0001重量未満では十分に掻性化
させるこずができず、良奜な化孊銅メツキ局を圢
成できなくなり、保枩性の向䞊を期埅できないか
らである。たた、貎金属塩を0.01重量以䞊の濃
床で䜿甚する堎合には未溶解塩が残るのを防止す
るため塩酞などを加えた溶液ずする必芁がある
が、それ以䞋の堎合でも塩酞などを加えおもよ
い。 化孊銅メツキ济ずしおは、アルカリ性銅溶液で
あれば、添加剀含有の有無にかかわりなく特に制
限はなく、垂販のものを䜿甚すればよい。 以䞋、本発明方法により補造されたステンレス
鋌補现口魔法瓶を瀺す添付の図面を参照しお具䜓
的に説明する。 図においお、はステンレス鋌補内容噚、は
ステンレス鋌補倖容噚で、䞡者はその口郚の郚
分でろう付けたたは溶接その他の手段により接合
しお二重壁構造を圢成し、内容噚ず倖容噚ず
の間に圢成される空間は排気されお真空にしお
ある。内容噚は胎郚ず底郚ずを溶接、
ろう付け等の手段により接合するこずによ぀お圢
成され、倖容噚は胎郚、底郚および肩
郚を接合するこずによ぀お圢成されおいる。
倖容噚の底郚には空間を真空にする際の
排気口ずなるチツプ管がろう付け等により接合
されおおり、このチツプ管を保護するために底
郚に底カバヌが接合剀により取り付けられ
おいる。なお、図瀺しおいないが、長期にわた぀
お高真空を保蚌する安党のために空間内にゲツ
タヌを配蚭するようにしおもよい。 他方、本発明に埓い、ステンレス鋌補真空二重
容噚の保枩力を向䞊させるため、空間を圢成す
る内倖䞡容噚の壁面、すなわち、内容噚の倖偎
衚面ず倖容噚の内偎衚面のうち、内容噚の倖偎
衚面に、第図に瀺すように、酞化被膜が圢成
され、その䞊に化孊銅メツキ局が積局されおい
る。なお、図瀺の実斜䟋においおは、内容噚の倖
偎衚面のみに化孊銅メツキ局が圢成されおいる
が、化孊銅メツキ局を内容噚の倖偎衚面ず倖容
噚の内偎衚面に圢成するようにしおもよい。これ
は内容量が小さい容噚の堎合の保枩性の向䞊を蚈
る䞊で特に有利である。 以䞋、本発明の実斜䟋に぀いお説明する。 実斜䟋  0.5mm厚のステンレス鋌SUS 304で内容量
750mlの内容噚を補䜜する䞀方、0.6mm厚のステ
ンレス鋌板で倖容噚の肩郚材、胎郚材
、底郚材を補䜜し、内容噚ず倖容噚の
肩郚材をそれらの口郚分で溶接し、これを
空気䞭にお350℃で30分焌成する。次いで、倖容
噚の胎郚材を焌成凊理した内容噚に溶接
するずずもに底郚材を溶接しお二重壁構造ず
し、倖容噚底郚に接合したチツプ管から空
間郚内に10ppmの塩化第錫を含む氎溶液を泚
入し、内容噚の倖衚面を感受性化させ、その氎
溶液を排出した埌、氎掗する。 次に、䞋蚘の凊方により調補した掻性化液をチ
ツプ管から空間内に泚入し、二重瓶を軞方向
に氎平に保持させ高速で回転させお内容噚ず倖
衚面を掻性化させる。 掻性化液の凊方 硝酞銀10を少量の氎に溶解させ、これに28
アンモニア氎500mlず氎を加えお4800mlずし、さ
らに氎酞化ナトリりム10を溶解させた氎溶液
200mlを加えお党量を5000mlずし、これを液ず
する。これずは別に、ぶどう糖の15氎溶液25ml
に氎を加えお党量を5000mlずし、これを液ずす
る。前蚘液ず液を容積比の割合で混合
した埌、該混合液100mlに察し、氎900mlを加えお
硝酞銀0.01重量を含む掻性化液ずする。 掻性化凊理した埌、排液、氎掗し、CuSO4・
5H2Oを35、NaOHを50、ロツセル
塩を170それぞれ含む溶液120mlず3.7ホル
マリン溶液120mlずを混合した化孊銅メツキ液240
mlを空間にチツプ管を介しお泚入し、二重瓶
を軞方向に氎平に保持させ、40℃で分間高速回
転させお、内容噚の倖衚面に第図に瀺す化孊
銅メツキ局を圢成させる。 次いで、氎掗し、150℃で也燥させた埌、真空
凊理し、チツプ管を溶封し、その底郚に底カバ
ヌを接合しお内容量0.75のステンレス鋌補魔
法瓶を埗た。 このようにしお埗たステンレス鋌補魔法瓶の保
枩力を調べるため、JISS2005に芏定される詊隓
法により䞋蚘条件で枬定したずころ、24時間の保
枩効力は63.0℃であ぀た。 詊隓条件 泚湯枩床95℃ 湯 量満 量 栓 密栓45mmφ 呚囲枩床20℃ なお、バフ研摩し脱脂した埌の詊隓片衚面の光
沢床は122で、焌成凊理埌の光沢床は101ず焌成前
に比べお21䜎䞋しおいた。この光沢床の倀は、
JIS Z8741に芏定される枬定法に基ずき、スガ詊
隓機(æ ª)補デゞタル倉角光沢蚈型匏UGV−
4Dを甚いお、入射角60°、暙準サンプルの光沢
床91.1を1/4の22.8に蚭定しお求めた倀である。 たた、これずは別に、0.3mm厚のステンレス鋌
SUS 304の詊隓片を衚に瀺す皮々の焌成条
件䞋で焌成埌、光沢床を枬定する䞀方、前蚘銀鏡
液を甚いお無電解メツキした。その結果も衚に
瀺す。
TECHNICAL FIELD The present invention relates to a method for manufacturing a stainless steel thermos flask. Prior Art In recent years, thermos flasks made of stainless steel have been put into practical use in place of glass thermos flasks that are susceptible to mechanical shock. In general, stainless steel has the advantages of not only high mechanical strength but also excellent corrosion resistance and low thermal conductivity, but like other metal materials, it releases gas from inside in a high vacuum, so it reduce the vacuum level of
Moreover, it has the disadvantage of large heat loss due to radiation. For this reason, attempts have been made to form a silver mirror on the wall of the thermos flask that forms the vacuum space between the inner container and the outer container, but unlike the case of glass thermos flasks, it is not possible to directly plate the stainless steel surface with a silver mirror. Since this is possible, it was proposed in JP-A-57-75621 to improve heat retention by applying nickel plating to the stainless steel surface and laminating a silver mirror plating layer thereon. The same publication also proposes laminating a chemical copper plating layer on the nickel plating layer. These thermos flasks have a plating layer that prevents heat dissipation due to radiation and suppresses gas release, so they exhibit sufficient heat retention performance for practical use and can maintain this temperature for a long period of time. Forming the plating layer requires a lot of attention and man-hours, and the process is complicated.
There was a problem with high manufacturing costs. As a result of various studies to solve this problem, we found that, contrary to the conventional wisdom that when plating a metal surface, the oil and oxide film on the metal surface must be removed to make the surface clean, it is necessary to sinter stainless steel. They discovered that by oxidizing the surface appropriately, it became possible to directly silver mirror plate the stainless steel surface.
We proposed a stainless steel vacuum double container using this technology. According to the manufacturing method described in the same specification, there is no need to nickel plate the stainless steel surface, and silver mirror plating can be achieved just by firing, reducing manufacturing costs and achieving good heat retention performance. However, since it is made of stainless steel, it was inevitable that the manufacturing cost would be higher than that of glass thermos flasks. Therefore, an inexpensive method of chemical copper plating instead of silver mirror plating was proposed in Japanese Patent Application No. 167207/1983. In this method, chemical copper plating is performed after firing stainless steel or by contacting it with an aqueous solution of a noble metal salt and then contacting it with stannous halide. When this method is applied to the manufacture of thermos flasks, It has become clear that although it is possible to form a chemical copper plating layer on the walls forming the vacuum space, this results in a fatal problem of significantly inferior heat retention compared to silver mirror plating. As a result of research into the cause, it was found that in the above method, undissolved noble metal salt particles exist in the noble metal salt aqueous solution that is contacted after firing, and these particles adhere to the surface of the substrate and roughen the plating layer, resulting in a homogeneous layer. It has become clear that heat dissipation due to radiation cannot be suppressed because the heat dissipation is not possible. OBJECT OF THE INVENTION The object of the present invention is to provide a method for manufacturing an inexpensive stainless steel thermos flask that has heat retention performance equal to or better than that of a stainless steel thermos flask whose walls forming a vacuum space are plated with silver mirrors. The technical problem is to prevent the surface of the chemical copper plating layer from becoming rough and to form a chemical copper plating layer with high emissivity. The gist of the present invention is to manufacture a stainless steel thermos flask that has a double wall structure consisting of an inner container and an outer container made of stainless steel, and in which the space formed between the two containers is evacuated. or the components thereof are fired in an oxidizing atmosphere, and then, among the surfaces of both containers forming the space, at least the surface of the inner container or the component parts of the inner container is sensitized, and then the noble metal salt is contained. A method for manufacturing a stainless steel thermos flask, characterized by activating it with an activating liquid and then chemically copper plating the flask. In other words, in the present invention, even if the stainless steel substrate is chemically plated with copper, the hydrogen generated on the surface of the substrate by the chemical reaction described below inhibits the precipitation of copper, and even if it does precipitate, it will crack or peel. Therefore, in order to form a copper plating layer with good adhesion to the surface of the stainless steel substrate, the inner container and the outer container, or the components of both containers, are oxidized. By firing in an atmosphere, a thin oxide film is formed on the surface forming the vacuum space, and a copper plating layer with high emissivity is uniformly deposited.
By sensitizing the oxide film and activating the surface with an aqueous solution of a precious metal salt such as an extremely low concentration of silver salt or palladium salt, or a solution containing a noble metal salt and an acid such as hydrochloric acid, chemical copper plating is performed. This solves the above technical problem. The chemical reaction in alkaline divalent copper solution is as follows. Cu ++ +2e - →Cu↓ 2HCHO+2OH - → 2HCOO - +2H 2 O+2e - +H 2 ↑ In a preferred embodiment of the present invention, in order to ensure strong adhesion of the copper plating layer to the stainless steel surface, the firing treatment is not performed. 250-550℃, preferably
It is carried out at 300 to 450°C, and the time varies depending on the temperature, but is usually 5 to 180 minutes, preferably
It lasts 10 to 60 minutes. Generally, the firing process is
in air or in an oxidizing atmosphere such as an oxygen-containing atmosphere at 250 to 550°C for 5 to 120 minutes, preferably,
It is carried out at 300-450°C for 10-60 minutes. This is because if the firing temperature is less than 250°C, a sufficient oxide film will not be formed or it will take a long time to form, inhibiting copper precipitation and increasing manufacturing costs; if the firing temperature exceeds 550°C, This is because the stainless steel base undergoes metamorphosis. The firing time can be set arbitrarily as long as it is within the above temperature range, but if it is less than 5 minutes, it will be difficult to form a sufficient oxide film when the firing temperature is low, and if it exceeds 180 minutes, it will not be necessary when the firing temperature is high. It is desirable to perform the firing within the above range because the above firing treatment increases energy loss and also inhibits the precipitation of copper again. The degree of oxidation of the stainless steel surface by this firing treatment is preferably such that the glossiness of the stainless steel surface after firing is 10 to 50 lower than the glossiness of the polished surface before firing. This means that the gloss reduction is 10
If the degree of oxidation is less than
This is because excessive oxidation, which decreases by more than 20%, makes it difficult to cause a copper precipitation reaction. The cause of this phenomenon has not been completely elucidated, but in unfired or similar conditions, sufficient ferric oxide, which contributes to copper precipitation, is not formed, and excessive oxidation causes surface This is presumed to be because ferric oxide ceases to exist in the steel, leaving almost only chromium oxide, which inhibits the precipitation of copper. Usually, as long as the firing is carried out under the above-mentioned firing conditions, the change in the glossiness of the stainless steel surface will fall within the above-mentioned range, so there is no need to particularly measure the glossiness after firing. Further, as the stainless steel, there is no problem in using any type of stainless steel such as austenitic, ferrite, steanite thread, etc. A chemical copper plating layer is formed on the oxide film, and can be formed by the following method. In other words, while increasing the copper precipitation rate,
In order to deposit uniformly, the oxide film is sensitized by wetting it with a sensitizing solution mainly composed of tin halide, and then activated with an activating solution containing a noble metal such as silver salt or palladium chloride. Formed by processing with copper plating solution. As the sensitizing solution, a bath containing stannous halide as the main component is used, and the sensitizing treatment is carried out for a short time, usually 1 to 5 minutes at room temperature, by immersion in the bath or by contacting with the sensitizing solution. This is done by As the activating solution, an aqueous solution containing precious metal salts such as silver salts and palladium salts at extremely low concentrations, or solutions containing noble metals and acids are used, but as noble metal salts, palladium chloride and silver oxides are economically advantageous. It is particularly preferred to use silver nitrate. In addition, the concentration of noble metal salt in the activation solution is 0.1 to 0.0001
% by weight, preferably from 0.01 to 0.005% by weight. This is because if the concentration of noble metal salt exceeds 0.1% by weight, not only will it cause an increase in cost, but it will also be difficult to dissolve it unless acid is added, making it difficult to obtain a uniform copper plating layer with high emissivity. This is because if it is less than 0.0001% by weight, it cannot be activated sufficiently, making it impossible to form a good chemical copper plating layer, and no improvement in heat retention can be expected. In addition, when using noble metal salts at a concentration of 0.01% by weight or more, it is necessary to add hydrochloric acid, etc. to the solution to prevent undissolved salts from remaining. Good too. The chemical copper plating bath is not particularly limited as long as it is an alkaline copper solution, regardless of whether it contains additives, and any commercially available bath may be used. Hereinafter, a detailed explanation will be given with reference to the accompanying drawings showing a stainless steel narrow neck thermos manufactured by the method of the present invention. In the figure, 1 is an inner container made of stainless steel, 2 is an outer container made of stainless steel, and both are joined at the mouth 3 by brazing, welding, or other means to form a double wall structure, and the inner container A space 4 formed between the container 1 and the outer container 2 is evacuated and made into a vacuum. The inner container 1 has a body part 1a and a bottom part 1b welded together,
The outer container 2 is formed by joining the body part 2a, the bottom part 2b, and the shoulder part 2c together by means such as brazing.
A tip tube 5, which serves as an exhaust port for evacuating the space 4, is bonded to the bottom 2b of the outer container 2 by brazing or the like, and a bottom cover 6 is bonded to the bottom 2b to protect the tip tube 5. It is attached by an agent. Although not shown, a getter may be provided in the space 4 for safety to ensure high vacuum over a long period of time. On the other hand, according to the present invention, in order to improve the heat retention ability of the stainless steel vacuum double container, among the walls of both the inner and outer containers forming the space 4, that is, the outer surface of the inner container 1 and the inner surface of the outer container 2, As shown in FIG. 2, an oxide film 7 is formed on the outer surface of the inner container, and a chemical copper plating layer 8 is laminated thereon. In the illustrated embodiment, the chemical copper plating layer is formed only on the outer surface of the inner container, but the chemical copper plating layer 8 is formed on the outer surface of the inner container and the inner surface of the outer container. Good too. This is particularly advantageous for improving heat retention in the case of containers with small contents. Examples of the present invention will be described below. Example 1 0.5mm thick stainless steel (SUS 304) with internal capacity
While manufacturing the 750ml inner container 1, the shoulder member 2c and body member 2 of the outer container 2 were made of 0.6 mm thick stainless steel plate.
a. The bottom member 2b is manufactured, the shoulder members 2c of the inner container 1 and the outer container 2 are welded together at their mouth portions 3, and this is baked in air at 350° C. for 30 minutes. Next, the body member 2a of the outer container 2 is welded to the fired inner container 1 and the bottom member 2b is welded to form a double wall structure, and 10 ppm is injected into the space 4 from the chip tube 5 joined to the outer container bottom 2b. An aqueous solution containing stannous chloride is injected to sensitize the outer surface of the inner container 1, and after the aqueous solution is discharged, it is washed with water. Next, an activation liquid prepared according to the following recipe is injected into the space 4 from the tip tube 5, and the double bottle is held horizontally in the axial direction and rotated at high speed to activate the inner container 1 and the outer surface. . (Prescription of activation liquid) Dissolve 10g of silver nitrate in a small amount of water, add 28%
Aqueous solution made by adding 500ml of ammonia water and water to make 4800ml, and further dissolving 10g of sodium hydroxide.
Add 200ml to make the total volume 5000ml, and use this as Solution A. Separately, 25 ml of a 15% aqueous solution of glucose
Add water to make a total volume of 5000ml, and use this as Solution B. After mixing the liquid A and liquid B at a volume ratio of 1:1, 900 ml of water is added to 100 ml of the mixed liquid to obtain an activation liquid containing 0.01% by weight of silver nitrate. After activation treatment, drain the liquid, wash with water, and remove CuSO4 .
Chemical copper plating solution 240, which is a mixture of 120 ml of a solution containing 35 g/5H 2 O, 50 g/NaOH, and 170 g Rotussel salt and 120 ml of 3.7% formalin solution.
ml was injected into the space 4 through the tip tube 5, the double bottle was held horizontally in the axial direction, and rotated at high speed for 5 minutes at 40°C to inject the chemical copper shown in Figure 2 onto the outer surface of the inner container 1. Form a plating layer. Next, after washing with water and drying at 150° C., vacuum treatment was performed, the tip tube 5 was melt-sealed, and a bottom cover 6 was joined to the bottom of the tube to obtain a stainless steel thermos flask having an internal capacity of 0.75. In order to examine the heat retention ability of the stainless steel thermos flask thus obtained, measurements were made under the following conditions using the test method specified in JISS2005, and the heat retention effect for 24 hours was 63.0°C. [Test conditions] Pouring temperature: 95℃ Hot water amount: Full Stopper: Sealed stopper (45mmφ) Ambient temperature: 20℃ The gloss of the test piece surface after buffing and degreasing was 122, and the gloss after baking treatment The temperature was 101, a decrease of 21 points compared to before firing. This gloss value is
Based on the measurement method specified in JIS Z8741, a digital variable angle gloss meter (Model: UGV-) manufactured by Suga Test Instruments Co., Ltd.
4D), the incident angle is 60°, and the standard sample's glossiness of 91.1 is set to 22.8, which is 1/4. Separately, after firing 0.3 mm thick stainless steel (SUS 304) test pieces under various firing conditions shown in Table 1, the gloss was measured, and electroless plating was performed using the silver mirror solution. did. The results are also shown in Table 1.

【衚】 実斜䟋  実斜䟋においお、掻性化液ずしお0.001重量
の塩化パラゞりム溶液を䜿甚した以倖は実斜䟋
ず同様にしお内容量750mlのステンレス補魔法
瓶を補䜜し、その保枩効力を枬定したずころ62.5
℃であ぀た。なお、0.001塩化パラゞりム溶液
は塩化パラゞりムを氎10に溶解させ、これ
を10倍に垌釈した甚意した。 比范䟋  実斜䟋においお、掻性化液ずしお0.01硝酞
銀溶液の代りに、䞋蚘組成の0.1塩化パラゞり
ム氎溶液を甚いた以倖は実斜䟋ず同様にしお同
じ条件䞋で内容量750mlのステンレス鋌補魔法瓶
を補䜜した。 掻性化液凊方 塩化パラゞりム 1.0 æ°Ž 1000ml この魔法瓶の24時間の保枩効力は50.6℃であ぀
た。 実斜䟋  0.5mm厚のステンレス鋌SUS 304で内容量
350mlの内容噚を補䜜する䞀方、0.6mm厚のステ
ンレス鋌板で倖容噚の肩郚材、胎郚材
、底郚材を補䜜し、内容噚ず倖容噚の
肩郚材をそれらの口郚分で溶接し、これを
空気䞭にお300℃で30分焌成する。次いで、これ
ずは別に倖容噚の胎郚材ず底郚材を溶
接しお䞀䜓化した組立䜓を焌成凊理した内容噚
に溶接しお二重壁構造ずし、倖容噚底郚に接
合したチツプ管から空間郚内に10ppmの塩化
第錫を含む氎溶液を泚入し、内容噚の倖衚面
を感受性化させ、その氎溶液を排出した埌、氎掗
する。 次に、実斜䟋ず同様にしお調補した0.01硝
酞銀掻性化液をチツプ管から空間内に泚入
し、二重瓶を軞方向に氎平に保持させ高速で回転
させお内容噚の倖衚面を掻性化させる。 掻性化凊理した埌、排液、氎掗し、実斜䟋で
調補した化孊銅メツキ液130mlを空間にチツプ
管を介しお泚入し、二重瓶を軞方向に氎平に保
持させ、40℃で分間高速回転させお、内容噚
の倖衚面に第図に瀺す化孊銅メツキ局を圢成さ
せる。 次いで、氎掗し、110℃で20分間也燥させた埌、
実斜䟋ず同様にしお真空凊理し、チツプ管を
溶封し、その底郚に底カバヌを接合しお内容量
0.35のステンレス鋌補魔法瓶を埗た。 このようにしお埗たステンレス鋌補魔法瓶の保
枩力を調べたずころ、24時間の保枩効力は45.0℃
であ぀た。詊隓条件は次の通りである。 詊隓条件 泚湯枩床95℃ 湯 量満 量 栓 密栓35mmφ 呚囲枩床20℃ 実斜䟋  実斜䟋においお、掻性化液ずしおブドり糖を
含有しない0.001重量の硝酞銀溶液130mlを甚い
お掻性凊理した以倖は実斜䟋ず同様にしおステ
ンレス鋌補魔法瓶を補䜜した。24時間での保枩効
力は45℃であ぀た。ちなみに、銀鏡局を圢成した
ものは44.9℃であ぀た。 効 果 以䞊の説明から明らかなように、本発明によれ
ば、埓来のニツケルメツキを介圚させる堎合のよ
うに煩雑な工皋を必芁ずせず、内倖瓶構成郚材を
焌成し、二重壁構造に組立おた埌、化孊銅メツキ
するだけでよいので䜜業性が向䞊し、しかも、銅
メツキは銀メツキ局を圢成する堎合に比べお安䟡
にでき、銀メツキ局を有するものず同等以䞊の保
枩力に優れた魔法瓶を補造するこずができるなど
優れた効果を奏する。たた、内倖瓶を焌成する過
皋においお、ステンレス鋌からの脱ガス䜜甚もあ
り、真空排気時間の短瞮になるずいう効果もあ
る。
[Table] Example 2 A stainless steel thermos flask with a content capacity of 750 ml was manufactured in the same manner as in Example 1 except that a 0.001% by weight palladium chloride solution was used as the activating liquid in Example 1, and its heat retention effect was measured. It turned out to be 62.5
It was warm at ℃. The 0.001% palladium chloride solution was prepared by dissolving 1 g of palladium chloride in 10 parts of water and diluting it 10 times. Comparative Example 1 The same procedure as in Example 1 was carried out, except that instead of the 0.01% silver nitrate solution in Example 1, a 0.1% aqueous palladium chloride solution having the following composition was used, under the same conditions, stainless steel with an internal volume of 750 ml was used. I made a thermos flask. (Activation liquid prescription) Palladium chloride 1.0g Water 1000ml The heat retention effect of this thermos bottle for 24 hours was 50.6°C. Example 3 0.5mm thick stainless steel (SUS 304) with internal capacity
While manufacturing the 350ml inner container 1, the shoulder member 2c and body member 2 of the outer container 2 are made of 0.6 mm thick stainless steel plate.
a. The bottom member 2b is manufactured, the shoulder members 2c of the inner container 1 and the outer container 2 are welded at their mouth portions 3, and this is baked in air at 300° C. for 30 minutes. Next, separately from this, the inner container 1 is produced by firing an assembly in which the body member 2a and the bottom member 2b of the outer container 2 are welded and integrated.
An aqueous solution containing 10 ppm of stannous chloride is injected into the space 4 from the chip tube 5 connected to the bottom part 2b of the outer container to sensitize the outer surface of the inner container 1. After draining the aqueous solution, wash with water. Next, 0.01% silver nitrate activation solution prepared in the same manner as in Example 1 was injected into the space 4 from the tip tube 5, and the double bottle was held horizontally in the axial direction and rotated at high speed to open the inner container 1. Activates the outer surface. After the activation treatment, the liquid was drained and washed with water, and 130 ml of the chemical copper plating solution prepared in Example 1 was injected into the space 4 through the tip tube 5, and the double bottle was held horizontally in the axial direction and heated to 40°C. Rotate at high speed for 5 minutes, then remove inner container 1.
A chemical copper plating layer shown in FIG. 2 is formed on the outer surface of the substrate. Then, after washing with water and drying at 110°C for 20 minutes,
Vacuum treatment was performed in the same manner as in Example 1, the chip tube 5 was melt-sealed, and the bottom cover 6 was bonded to the bottom of the tube to determine the internal capacity.
I got a 0.35 stainless steel thermos. When we investigated the heat retention ability of the stainless steel thermos flask obtained in this way, the heat retention effect for 24 hours was 45.0℃.
It was hot. The test conditions are as follows. [Test conditions] Water pouring temperature: 95℃ Hot water amount: Full stopper: Sealed stopper (35mmφ) Ambient temperature: 20℃ Example 4 In Example 3, 130ml of a 0.001% by weight silver nitrate solution that does not contain glucose was used as the activation liquid. A stainless steel thermos flask was produced in the same manner as in Example 2, except that the activation treatment was carried out using the same method as in Example 2. The heat retention effect for 24 hours was 45°C. By the way, the temperature of the one with the silver mirror layer was 44.9°C. Effects As is clear from the above explanation, according to the present invention, the inner and outer bottle components are fired and assembled into a double-walled structure without the need for a complicated process unlike the case of using conventional nickel plating. After that, it is only necessary to apply chemical copper plating, which improves work efficiency.Moreover, copper plating is cheaper than forming a silver plating layer, and it has excellent heat retention properties that are equal to or better than those with a silver plating layer. It has excellent effects such as being able to manufacture thermos flasks. Additionally, in the process of firing the inner and outer bottles, there is also a degassing effect from the stainless steel, which has the effect of shortening the evacuation time.

【図面の簡単な説明】[Brief explanation of drawings]

第図は本発明方法により補造されたステンレ
ス鋌補魔法瓶の断面図、第図は第図の郚拡
倧図である。 〜内容噚、〜倖容噚、〜空間、〜酞化
被膜、〜化孊銅メツキ局。
FIG. 1 is a sectional view of a stainless steel thermos flask manufactured by the method of the present invention, and FIG. 2 is an enlarged view of section A in FIG. 1. 1 - inner container, 2 - outer container, 4 - space, 7 - oxide film, 8 - chemical copper plating layer.

Claims (1)

【特蚱請求の範囲】  ステンレス鋌補の内容噚ず倖容噚ずからなる
二重壁構造を有し、䞡容噚間に圢成される空間を
真空にしおなるステンレス鋌補魔法瓶を補造する
に際しお、䞡容噚たたはそれらの構成郚品を酞化
性雰囲気䞭で焌成し、次いで、前蚘空間を圢成す
る䞡容噚の衚面のうち少なくずも内容噚たたは内
容噚の構成郚品の衚面を感受性化凊理した埌、貎
金属塩を含有する掻性化液で掻性化させ、次いで
化孊銅メツキさせるこずを特城ずするステンレス
鋌補魔法瓶の補造方法。  前蚘焌成を空気䞭250〜550℃で行なう特蚱請
求の範囲第項蚘茉の方法。  内容噚のみを焌成する特蚱請求の範囲第項
たたは第項蚘茉の方法。  感受性化凊理を塩化第錫含有溶液で行なう
特蚱請求の範囲第項〜第項のいずれか䞀項蚘
茉の方法。  掻性化液が硝酞銀を0.1〜0.0001重量含有
する特蚱請求の範囲第項〜第項のいずれか䞀
項蚘茉の方法。  掻性化液が塩化パラゞりムを0.1〜0.0001重
量含有する特蚱請求の範囲第項〜第項のい
ずれか䞀項蚘茉の方法。
[Scope of Claims] 1. When manufacturing a stainless steel thermos flask that has a double wall structure consisting of an inner container and an outer container made of stainless steel, and in which the space formed between the two containers is evacuated, After firing the container or its component parts in an oxidizing atmosphere, and then sensitizing at least the surface of the inner container or the component parts of the inner container among the surfaces of both containers forming the space, containing the noble metal salt. A method for producing a stainless steel thermos flask, which comprises activating the flask with an activating solution and then chemically copper plating the flask. 2. The method according to claim 1, wherein the firing is performed in air at 250 to 550°C. 3. The method according to claim 1 or 2, in which only the inner container is fired. 4. The method according to any one of claims 1 to 2, wherein the sensitization treatment is performed with a solution containing stannous chloride. 5. The method according to any one of claims 1 to 4, wherein the activating solution contains 0.1 to 0.0001% by weight of silver nitrate. 6. The method according to any one of claims 1 to 5, wherein the activation liquid contains 0.1 to 0.0001% by weight of palladium chloride.
JP2783384A 1984-02-15 1984-02-15 Production of stainless steel thermos Granted JPS60171019A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2783384A JPS60171019A (en) 1984-02-15 1984-02-15 Production of stainless steel thermos

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2783384A JPS60171019A (en) 1984-02-15 1984-02-15 Production of stainless steel thermos

Publications (2)

Publication Number Publication Date
JPS60171019A JPS60171019A (en) 1985-09-04
JPH0415686B2 true JPH0415686B2 (en) 1992-03-18

Family

ID=12231933

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2783384A Granted JPS60171019A (en) 1984-02-15 1984-02-15 Production of stainless steel thermos

Country Status (1)

Country Link
JP (1) JPS60171019A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5027891B2 (en) * 2010-01-06 2012-09-19 株匏䌚瀟 資生堂 Analysis method
WO2011083730A1 (en) * 2010-01-06 2011-07-14 株匏䌚瀟資生堂 Reference material for nmr, sample tube for nmr, capillary for nmr, and method for determining nmr spectrum of sample
JP4923112B2 (en) * 2010-01-06 2012-04-25 株匏䌚瀟 資生堂 External standard for 1H NMR

Also Published As

Publication number Publication date
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