JPS59190227A - Reduction of fe3+ by contact of different metals - Google Patents

Reduction of fe3+ by contact of different metals

Info

Publication number
JPS59190227A
JPS59190227A JP6456683A JP6456683A JPS59190227A JP S59190227 A JPS59190227 A JP S59190227A JP 6456683 A JP6456683 A JP 6456683A JP 6456683 A JP6456683 A JP 6456683A JP S59190227 A JPS59190227 A JP S59190227A
Authority
JP
Japan
Prior art keywords
metal
reduction
iron
contact
reaction
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.)
Pending
Application number
JP6456683A
Other languages
Japanese (ja)
Inventor
Hidejiro Asano
朝野 秀次郎
Akimi Umezono
梅園 昭己
Hironobu Kawasaki
川崎 博信
Tomohiko Hayashi
林 知彦
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.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
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 Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP6456683A priority Critical patent/JPS59190227A/en
Publication of JPS59190227A publication Critical patent/JPS59190227A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:In reducing Fe<3+> in an acidic aqueous solution using Fe or a metal baser than Fe, to reduce Fe<3+> efficiently and rapidly, by bringing a metal such as Pb, Ag, or Au except Fe and Os of VIII group or Sn into contact with the metal. CONSTITUTION:Fe<3+> ion in an acidic aqueous solution is reduced by using one or both of Fe and a metal such as Zn, Al, Mn, or Mg baser than Fe. In the operation, one or more of Pt, Pd, Rh, Ru, Ir, Pb, Sn, Ag, Au, Ni, and Co or its alloy as a metal catalyst is brought into contact with the metal. The metal and the metal catalyst can be used in various kinds of state such as powder, platy state, etc.

Description

【発明の詳細な説明】 本発明は水溶液中のFe  イオンを鉄もしくは鉄より
楯1な金シくを用いて還元する際に触媒として異種金属
を接触させて効率よく還元を行な・う方法に関するもの
である。
[Detailed Description of the Invention] The present invention provides a method for efficiently reducing Fe ions in an aqueous solution by bringing different metals into contact with each other as a catalyst when using iron or a gold film that is stronger than iron. It is related to.

]パCイオンを酸性水溶液中で鉄より卑な金属Δ1を用
いて1illt元すると一般に下記の反応がおこる。
] When PaC ions are converted to 1 illt using a metal Δ1 which is less noble than iron in an acidic aqueous solution, the following reaction generally occurs.

、n](’c 1−ゞ“−°1°+M″   −゛(1
,)(・ロイ−+  M  =  u Ij2 +  
Mn+        −−(2)即ち(1)の反応の
みおこるとすれは気体水素の発生がなく、効率100%
てFe  をFc  に還元することが可能である。し
かし一般的には(2)の反応も発生し、気体水素が発生
すれはするほど水素イオンの減少即ちpHの上昇をまね
き、還元速度の低下と共に還元の効率も低下する。
,n]('c 1-ゞ"-°1°+M"-゛(1
,)(・Roy−+M=u Ij2+
Mn+ --(2), that is, if only the reaction (1) occurs, no gaseous hydrogen is generated, and the efficiency is 100%.
It is possible to reduce Fe to Fc. However, in general, the reaction (2) also occurs, and the more gaseous hydrogen is generated, the more hydrogen ions are generated, that is, the pH increases, and the reduction rate and the reduction efficiency are also lowered.

従来からFe  イオンを還元する方法として、水銀と
鉄より卑で水銀とアマルガムを形成する金属を用いて行
なう方法が特に化学分析などで行なわれている。水銀な
いし水銀アマルガムは水素過電圧が非常に高く水素が発
生しにくいので、前述の(2)の反応はほとんどおこら
ず、したがって(1)の反応が主体となり還元効率とい
う点ては非常によい方法である。しかし還元反応の速度
については非常におそく、工業的に大量のFe  イオ
ンを還元するという観点からは好荻しい方法ではない。
Conventionally, as a method for reducing Fe 2 ions, a method using a metal that is more base than mercury and iron and forms an amalgam with mercury has been used, particularly in chemical analysis. Since mercury or mercury amalgam has a very high hydrogen overvoltage and is difficult to generate hydrogen, the above-mentioned reaction (2) hardly occurs, and therefore the reaction (1) is the main one, making it a very good method in terms of reduction efficiency. be. However, the speed of the reduction reaction is very slow, and it is not a desirable method from the viewpoint of industrially reducing a large amount of Fe 2 ions.

一方法より枠な金属Mて還元する場合にはFe3+イオ
ン0遺りによって生成したFc  イオンが用いたM1
属表面に金属鉄として以下の反応により析出してくる。
In the case of reduction using a metal M which is more basic than the other method, the Fc ions generated by the Fe3+ ion and the M1 used are
It is precipitated as metallic iron on the metal surface by the following reaction.

2+ nFe   + ’2M  =  nFe  +  2
へ□r     −−(3)鉄及び鉄より卑な金属で還
元する場合には、いずれにしても鉄表面での還元反応が
重要となる。
2+ nFe + '2M = nFe + 2
(3) When reducing with iron or a metal less noble than iron, the reduction reaction on the iron surface is important in any case.

鉄を用いて酸性水溶液中でFc  を還元すると、単位
表面積当りの鉄の還元速度は一般に減少してくる。また
鉄より卑な金属を用いた場合も同様に鉄表面での反応か
主体となり還元反応速度は時間と共に減少する。これは
離解したあとの鉄表面は非常に活訃か強く、その上に何
らかの保護皮膜(j・1女化皮膜と考えられる)が直ち
に形成されてしま・うためと考えられる。
When iron is used to reduce Fc in an acidic aqueous solution, the reduction rate of iron per unit surface area generally decreases. Similarly, when a metal less noble than iron is used, the reaction is mainly carried out on the iron surface, and the reduction reaction rate decreases with time. This is thought to be because the iron surface after disintegration is very active and strong, and some kind of protective film (possibly a j.1 feminized film) is immediately formed on it.

本発明者らはこのような状態になることをさけるために
、鉄より電位的に貴で、還元活性の強い金属触媒をFe
ないし前述の金属Mに接触さぜれは、金1ドアのイオン
への溶解はFeないし金属M表面上でおこり、金1(j
’4イオン溶解によって出来た○は金属触媒面上にうつ
り、そこでFe  の還元反応及び気体水素の発牛舎行
なわせることができるであろうと考えた。この方法によ
れは還元を行なうべき表面の反応活性か前述のように低
下することなく、活性のつよい触媒金属表面で行えるこ
とが期待される。触媒という観点からは、反応中に金属
成分が溶解することは好ましくない。−力気体水素の発
生もおこる可能性もあるので、その発生反応をできるた
けおさえることが必要である。以上の点に留意しながら
種々検討した結果、Pi、Pd、Ru。
In order to avoid this situation, the present inventors used a metal catalyst that is nobler in potential than iron and has stronger reduction activity than Fe.
When it comes into contact with the metal M or the metal M mentioned above, the dissolution of gold 1 door into ions occurs on the surface of Fe or the metal M, and the gold 1(j
It was thought that the ○ formed by the dissolution of the '4 ion would be transferred onto the metal catalyst surface, where the reduction reaction of Fe and gaseous hydrogen generation would be carried out. With this method, it is expected that reduction can be carried out on a highly active catalytic metal surface without reducing the reaction activity of the surface to be reduced as described above. From the point of view of the catalyst, it is undesirable for metal components to dissolve during the reaction. - Gaseous hydrogen may also be generated, so it is necessary to suppress this reaction as much as possible. As a result of various studies while keeping the above points in mind, Pi, Pd, and Ru were selected.

RIB、Ir、Pb、Sn、A、g、Au及びNi、C
o の] l!1sまたは数種ないしこれらの合金を接
触触媒として用いれは、常に還元活性の強い面かえられ
還元反応速度か早く、しかも気体水素の発生が少なく効
率のよい還元が行えることを見い出した。
RIB, Ir, Pb, Sn, A, g, Au and Ni, C
o's] l! It has been found that when 1S or several kinds or alloys thereof are used as a catalytic catalyst, the reduction activity is always strong, the reduction reaction rate is fast, gaseous hydrogen is generated little, and reduction can be carried out efficiently.

本発明において用いる鉄および/または鉄より卑な金属
としては、鉄の他亜鉛、アルミニ・クム、マンガン、マ
クネシウムなどの金属で、形状としては粉末状、粒状、
綿状、チップ状、板状などの形態のものを用いることが
できる一方これに接触する金属触媒としてのPi、Pd
、]]1−h、11.u、Ir、Pb。
In addition to iron, iron and/or metals baser than iron used in the present invention include metals such as zinc, aluminum cum, manganese, and magnesium, and are in the form of powder, granules,
It can be in the form of cotton, chips, plates, etc., while Pi, Pd as the metal catalyst in contact with this can be used.
,]]1-h, 11. u, Ir, Pb.

S11.Ag、AuあるいはNi、Coないしこれらの
合金も同じく粉末状、粒状、綿状、板状などの種々の形
態のものを使用することができる。異種金属同志よく接
触させる(めにlQp媒の形状を更にかえて、金網、ラ
セン、かごな(!:種々の形状にすることも可能である
。更にまた異種の金属の上にこれらの金属をめっきした
ものも使用できる。一般的に溶解する金属ならびに触媒
金属の表面積はできるたけ大きくとった方が反応速度も
大きくまた還元効率においても良い方向にあるか、還元
装置、異種金属の接触等を考慮に入れて形状をえらぶべ
きである。
S11. Ag, Au, Ni, Co, or their alloys can also be used in various forms such as powder, granules, cotton, and plate. It is also possible to bring different metals into good contact with each other (it is also possible to further change the shape of the Qp medium to make it into various shapes such as a wire mesh, a spiral, and a cage (!). Plated metals can also be used.Generally speaking, the larger the surface area of the metal to be dissolved and the catalyst metal, the higher the reaction rate and the better the reduction efficiency. The shape should be selected with this in mind.

本発明は特に、鉄系のめつき液でFe  が生成すると
電析効率がFす、めっき皮膜の性状にも悪影響を及はす
ような場合に適用でき、この際に本発明の触媒を用いる
と効率よくしかも速やかにFe  を還元することがで
きる。
The present invention is particularly applicable to cases where the production of Fe in an iron-based plating solution reduces the electrodeposition efficiency and adversely affects the properties of the plating film, and in this case, the catalyst of the present invention is used. Fe can be reduced efficiently and quickly.

更にまた本発明はその他分析にも金属イオンの分姉等に
も幅広く適用できるものである。
Furthermore, the present invention can be widely applied to other analyzes and to the analysis of metal ions.

実施例1 1・′e  イオン56 ! / iを含むpH1,0
液昌500Cの硫酸酸性水溶液中のFe  イオンを金
属の鉄及び亜鉛史に金属触媒を用いて還元を行なった。
Example 1 1・'e ion 56! / pH 1,0 including i
Fe ions in a sulfuric acid acidic aqueous solution of Suisho 500C were reduced to metals iron and zinc using a metal catalyst.

水溶液の量を100cc、  この液中に含まれるFe
  5.6.i’を理論上100%還元するに必要な鉄
として2.8!、亜鉛として3.21を用いて鉄または
即鉛か完全に消失するまて還元を行なった≦反応終了後
残存しているFe  イオンを分析し、還元効率を算出
した。
The amount of aqueous solution is 100cc, and the Fe contained in this liquid is
5.6. The amount of iron required to theoretically reduce i' to 100% is 2.8! Reduction was carried out using 3.21 as zinc until the iron or ready lead completely disappeared.≦After the reaction, the remaining Fe ions were analyzed and the reduction efficiency was calculated.

一方この系に触媒と各種金属をFc及びZnに接触させ
た系につき同様の実験を行なった1、得られた結果を第
1表に示す。表からも水銀アマルガムは還元効率はよく
ても反応速度は非常におそく、工業的な意味での実用性
に乏しいことがわかる。一方触媒出考えられる’]” 
i 、 Cu 、  カーボン+ Mo なとは反応時
間は促進させるが、還元効率の点て本発明のPt、Pd
、Au、Ni 、Ag、Co  などに劣ること力脣2
召められた。
On the other hand, a similar experiment was conducted on a system in which a catalyst and various metals were brought into contact with Fc and Zn1.The results obtained are shown in Table 1. From the table, it can be seen that although mercury amalgam has good reduction efficiency, the reaction rate is very slow, and it is not practical in an industrial sense. On the other hand, it can be considered that the catalyst comes out
i, Cu, carbon + Mo accelerate the reaction time, but in terms of reduction efficiency, Pt, Pd of the present invention
, Au, Ni, Ag, Co etc.
I was called.

第1表 金属溶解による n’Ni50%−Co50%の合金 3+ Fe  イオンの還元 実施例2 3+ Fe  207//12を含む水溜液を金属推鉛粒(粒
径2 mm〜3 rnm )を用いて下肥の条件で還元
する際に白金触媒の使用の41無による比較を行なった
Table 1 Reduction of n'Ni50%-Co50% alloy 3+ Fe ions by metal dissolution Example 2 A water reservoir containing 3+ Fe 207//12 was treated using metal thrust particles (particle size 2 mm to 3 rnm). A comparison was made between the use of a platinum catalyst and the use of a platinum catalyst during reduction under manure conditions.

水溶液組成 Fc   20j;’/12    液−
計50012]、’c  60!/ノ Zn  80!/ll ll2So、酸性 pH1,2瀞度50℃還元装置  
200mmψの円[≦)状反応イA11jに11]1鉛
粒]1(9を充j道しそこ(こゴニa己の液を1.5m
/秒の流速で通過させる。
Aqueous solution composition Fc 20j;'/12 liquid-
Total 50012], 'c 60! /ノZn 80! /ll ll2So, acidic pH 1,2 temperature 50℃ reduction equipment
200mmψ circle [≦)-shaped reaction A11] 1 lead grain] 1
Passed at a flow rate of /sec.

白金触媒は]mmψ×3〜511i1#の線状チップを
10.5.f’加えて反応させた。
For the platinum catalyst, a linear chip of mmψ×3 to 511i1# was prepared with a diameter of 10.5 mm. f' was added and reacted.

(4fられた結果を第2表に示す。(The results obtained are shown in Table 2.

第2表から白金触媒を使用すると音元反応速1並か増加
すると共に還元効率も向上することか1.忍められる、
From Table 2, it can be seen that when a platinum catalyst is used, the sonic reaction rate increases by about 1, and the reduction efficiency also improves.1. can be tolerated,
.

第2表 流動槽使用による1・Cの還元− − − 1゜ −Table 2: Reduction of 1・C by using a fluidized tank - − − 1゜ −

Claims (1)

【特許請求の範囲】 V、およU/または鉄より卑な金属を用いて酸性水流液
中のFc  イオンを還元する際に、P L ’、 P
 d 。 Rh、11.u、■rj〕l:+、Sn、Ag、Au、
Ni 、Coのうち1種又は数種ないしこれらの°合金
を前記金属と接触さぜた状態で還元することを特徴とす
る異種金属接触によるFc  還元法。
[Claims] When reducing Fc ions in an acidic aqueous solution using V, and U/or a metal less noble than iron, P L ', P
d. Rh, 11. u, ■rj]l:+, Sn, Ag, Au,
An Fc reduction method by contact with different metals, characterized in that one or more of Ni, Co, or an alloy thereof is reduced in a state in which it is brought into contact with the metal.
JP6456683A 1983-04-14 1983-04-14 Reduction of fe3+ by contact of different metals Pending JPS59190227A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6456683A JPS59190227A (en) 1983-04-14 1983-04-14 Reduction of fe3+ by contact of different metals

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6456683A JPS59190227A (en) 1983-04-14 1983-04-14 Reduction of fe3+ by contact of different metals

Publications (1)

Publication Number Publication Date
JPS59190227A true JPS59190227A (en) 1984-10-29

Family

ID=13261904

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6456683A Pending JPS59190227A (en) 1983-04-14 1983-04-14 Reduction of fe3+ by contact of different metals

Country Status (1)

Country Link
JP (1) JPS59190227A (en)

Similar Documents

Publication Publication Date Title
EP0363552B1 (en) Process for preparing metal particles
JPS6285500A (en) Electromagnetic interference shielding material
JPS6111130A (en) Novel minute aggregate of metal being not noble metal and its production
KR20070051777A (en) Systhesis of nanosized metal particles
JPH06292830A (en) Hydrogenating catalyst for use in hydrogen peroxide process, method for preparation thereof and method for hydrogenating anthraquinone or derivative thereof
JP6096816B2 (en) Catalyst production method and production apparatus
JPS59120249A (en) Preparation of noble metal catalyst
JPH0557324B2 (en)
JPS59190227A (en) Reduction of fe3+ by contact of different metals
JP2011089156A (en) Metal fine particle, and method for producing the same
JPH0830204B2 (en) Method for producing fine metal powder
US6110254A (en) Method for chemical precipitation of metallic silver powder via a two solution technique
CN110919019A (en) Preparation method of high-purity ruthenium powder
JPH01139710A (en) Manufacture of fine granular alloy powder
JPH07502787A (en) Silver-metal oxide materials used in electrical contacts
US4167240A (en) Method of treating an electroplating solution comprising ions of gold and cyanide prior to electroplating and thermocompression bonding
JPH10121156A (en) Metallic ion treating agent and treatment of noble metallic complex ion
GB1401081A (en) Powder mixture of metal silver and gold and process for making same
JPH06299363A (en) Plating method with tin
JP2877410B2 (en) Preparation method of noble metal fine particles
JPS6357703A (en) Production of fine metallic powder
JPS6366369B2 (en)
JPS6122028B2 (en)
JPS63137128A (en) Acid treatment of manganese nodule
JP2969728B2 (en) Powder alloying method