CN104651880B - 一种脱铜分氰联立工艺处理银冶炼含氰贫液的方法 - Google Patents
一种脱铜分氰联立工艺处理银冶炼含氰贫液的方法 Download PDFInfo
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- CN104651880B CN104651880B CN201510058977.3A CN201510058977A CN104651880B CN 104651880 B CN104651880 B CN 104651880B CN 201510058977 A CN201510058977 A CN 201510058977A CN 104651880 B CN104651880 B CN 104651880B
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N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 title claims abstract description 60
- 238000000034 method Methods 0.000 title claims abstract description 33
- 241000412565 Argentina sphyraena Species 0.000 title claims abstract description 10
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- 239000000243 solution Substances 0.000 claims description 54
- PMZURENOXWZQFD-UHFFFAOYSA-L na2so4 Chemical compound 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[Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 26
- BQCADISMDOOEFD-UHFFFAOYSA-N silver Chemical compound 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[Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 18
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 13
- 235000011152 sodium sulphate Nutrition 0.000 claims description 13
- 238000000605 extraction Methods 0.000 claims description 11
- VWDWKYIASSYTQR-UHFFFAOYSA-N Sodium nitrate Chemical compound 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[Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 claims description 10
- -1 Copper zinc Chemical compound 0.000 claims description 9
- FGIUAXJPYTZDNR-UHFFFAOYSA-N Potassium nitrate Chemical class 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h0Pgo8L3N2Zz4K [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 238000007710 freezing Methods 0.000 claims description 6
- OTYBMLCTZGSZBG-UHFFFAOYSA-L Potassium sulfate Chemical compound 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[K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 claims description 5
- 150000001450 anions Chemical class 0.000 claims description 5
- 229910052939 potassium sulfate Inorganic materials 0.000 claims description 5
- 235000011151 potassium sulphates Nutrition 0.000 claims description 5
- 235000010344 sodium nitrate Nutrition 0.000 claims description 5
- 239000004317 sodium nitrate Substances 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 3
- 235000010333 potassium nitrate Nutrition 0.000 claims description 3
- 239000004323 potassium nitrate Substances 0.000 claims description 3
- 229910001431 copper ion Inorganic materials 0.000 claims description 2
- JPVYNHNXODAKFH-UHFFFAOYSA-N cu2+ Chemical compound 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- 238000004090 dissolution Methods 0.000 claims description 2
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[Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 9
- 229910052737 gold Inorganic materials 0.000 description 9
- 239000010931 gold Substances 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound 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- DOBRDRYODQBAMW-UHFFFAOYSA-N Copper(I) cyanide Chemical group 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[Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 2
- 239000005092 Ruthenium Substances 0.000 description 2
- 238000003723 Smelting Methods 0.000 description 2
- VGTPCRGMBIAPIM-UHFFFAOYSA-M Sodium thiocyanate Chemical compound 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[Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 2
- PXXJCXVYUXPAOS-UHFFFAOYSA-N [Zn].[Cu].N#CC#N Chemical compound 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- 238000007654 immersion Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000003014 ion exchange membrane Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M isothiocyanate Chemical compound 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[S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- 239000010808 liquid waste Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000001728 nano-filtration Methods 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N nitric acid Chemical compound 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O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
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[Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000010129 solution processing Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C1/00—Electrolytic production, recovery or refining of metals by electrolysis of solutions
- C25C1/12—Electrolytic production, recovery or refining of metals by electrolysis of solutions of copper
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B11/00—Obtaining noble metals
- C22B11/08—Obtaining noble metals by cyaniding
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25C—PROCESSES FOR THE ELECTROLYTIC PRODUCTION, RECOVERY OR REFINING OF METALS; APPARATUS THEREFOR
- C25C7/00—Constructional parts, or assemblies thereof, of cells; Servicing or operating of cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Abstract
本发明提供一种脱铜分氰联立工艺处理银冶炼含氰贫液的方法,含氰贫液进电解阴极室,含碱或盐的溶液进电解槽的阳极室,电解槽阴极和阳极之间加阳离子交换膜,阳离子通过膜进入阴极室,实现电路回路的联通,阴极室中电解析出铜和CN‑,电解阴极室储槽中CN‑含量较高时转移到电渗析淡水储槽,在电渗析淡水室中CN‑离子被转移并浓缩到电渗析浓水室,而等络离子不能被通过膜,电渗析淡水储槽中的CN‑离子浓度较低时,将其返回电解阴极室储槽,再电解析出金属铜和CN‑。当电渗析淡水储槽中的CN‑、离子浓度都较低时,将其转入电渗析浓水储槽作为电渗析浓水。电渗析浓水储槽中的CN‑浓度较高时将其送回银浸出工序。
Description
一种脱铜分氰联立工艺处理银冶炼含氰贫液的方法
技术领域
[0001] 本发明属于白银冶炼工业领域,涉及一种氰化法银冶炼含氰贫液处理和回用的方 法,特别是用包括电渗析、电解、冷冻等工艺结合,除去含氰贫液中的杂质,回收贫液中的氰 根并回用的方法和装置。
背景技术
[0002] 在银冶炼工业,尽管氰化物提取工艺有剧毒,但因其生产成本低,提取率高,速度 快,工艺成熟,仍是目前白银生产的首选方案。为了减少含氰提取贫液对环境的污染,其提 取贫液必须回用,而含氰贫液长期的回用造成其中的其它金属和盐类等杂质大量积累,影 响了银的提取率。氰化浸出液在提金或提银后循环使用,导致杂质积累从而使氰化液浸金 浸银能力(即活性)降低的现象称之为氰化液的疲劳,产生活性降低的原因是这些杂质离子 在金、银表面生成不同类型的膜,阻碍了 CN'O2的扩散。氰化液中的铜、锌、铁的氰化络阴离 子在金银表面生成膜的特性及机理大致相同,这些络合阴离子被金银表面吸附并转变成各 自的氰化物膜,所生成膜的孔隙度差别很大,最致密的膜为CuCN,CN1P02不易通过此膜,而 Fe (CN) 2膜是松散易透过的,Zn (CN) 2膜介于这两者之间,因此阻碍氰化浸出金的作用按Fe、 Zn、Cu的顺序增强。含氰化液的疲劳,影响了企业的经济效益。为解决此问题,国内外研究机 构进行了很多研究工作,但仍没有成熟有效的方法。
[0003] 现有的含氰贫液处理和回用的方法有酸化-氧化工艺和电积法等等。酸化-氧化工 艺(崔学奇等,氰化厂浸金贫液除杂工艺生产实践,黄金,2012,22 (12) : 45-47)先用硫酸将 贫液PH值调为2,吹出HCN并用碱回收,同时使其中的铜沉淀出来;再将pH调为碱性,用氧化 剂如臭氧或双氧水使SC『氧化,使其他金属阳离子沉淀出来。这种工艺需先加入硫酸调低 pH,产生的HCN毒性很大,难以控制,而且需再用碱调高pH值,非常繁琐,在贫液中加入的酸 和碱最终生成硫酸钠,硫酸钠在冬季易于析出堵塞管道,对生产造成严重影响。电积法(胡 湖生等,从高铜氰溶液中电积铜和锌,化工冶金,2000,21 (3) :257-262)是对萃取浓缩后的 贫液进行电解,负极得到粗铜或者铜锌混合物,但其正极将Cf氧化掉,造成Cf损失,增加了 生产成本,所以该技术基本没有得到工业应用。文献(胡湖生等,电积一酸化法从高铜氰溶 液中回收铜氰锌,有色金属,2000,52 (3) : 61-65)提出了电积-酸化工艺,先电积锌,再酸化, 再电积得到铜,这种方法仍需向体系中加入大量的硫酸,且需要将HCN吹除后再吸收回用, 操作麻烦,损失大,成本高。董德喜等(含氰废液酸化沉淀物综合回收试验研究,黄金,2005, 26 (9) : 38-41)提供了一种将含氰贫液酸化,而废渣煅烧回收铜的工艺,其工艺流程复杂,生 产成本较高。雷兆武等(含铜废水的膜电解,膜科学与技术,2012,32 (2) :96-99)提出了膜电 解的工艺,即在阴极和阳极之间加一块阳离子交换膜,对含铜废水进行电解,该工艺处理的 铜浓度低,对于含氰贫液则无法处理,因为在含氰贫液中,铜和锌均与氰根形成络合物,不 能通过离子交换膜,无法进行连续电解。李春旺(膜分离在氰化贫液处理中的应用与研究, 北京工业大学,硕士学位论文,2004,3),研究了超滤、纳滤、反渗透在含氰贫液中的应用,但 其研究的体系含铜锌离子较低,其处理的废液浓度一般为400_600mg/L,处理后的浓水中铜 锌离子浓度约为3000-4000mg/L,而银提取实际生产时含氰贫液原水中铜锌含量一般在 5000-7000mg/L,在此浓度下,反渗透的操作压力很大,水的收率很低,是不能工业化应用 的。也有文献报道用H2O2等氧化物氧化含氰贫液,将其中的Cf首先氧化为CN(T,再进一步氧 化为⑶,,调节pH沉淀铜锌金属阳离子,这种工艺损失了 CN,从经济的角度看是不合理的 (氰化厂浸金贫液除杂工艺生产实践,黄金,2001,22 (12) :45-46)。
[0004] 虽然各种研究的报告很多,但是工业应用的多是先酸化沉淀,再中和回用的工艺, 这种工艺在工业应用时成本高,冬季输送管道堵塞,操作危险性大,因此急需一种新的处理 工艺。
发明内容
[0005] 针对现有技术的不足,本发明的目的是提供一种能将银冶炼贫液中的铜和氰同时 脱除并分离的技术:脱铜分氰联立工艺处理金银冶炼含氰贫液,释放CN'实现水回用的方 法。本发明目的在于解决银提取生产中含氰贫液的处理和水回的问题,实现铜、锌和Cf的 回收,使含氰贫液得到回用。
[0006] 本发明采用了包括电渗析、电解等工艺结合的方法,能够将含氰贫液中的铜锌等 重金属离子分离除去,同时将电解游离出来的氰根分离除去回用,又通过常规的冷冻结晶 工艺使溶液中的硫酸钠也得到分离。
[0007] 本发明采用的方案是:一种脱铜分氰联立工艺处理银冶炼含氰贫液的方法,将电 解与电渗析联合操作,含氰贫液预先加入电解阴极室储罐,再进电解阴极室,含碱或盐的阳 极溶液预先存于电解阳极室储槽,再进电解槽的阳极室,电解槽阴极和阳极之间加阳离子 交换膜,阳离子通过膜进入阴极室,实现电路回路的联通,阴极室电解产生的阴离子不通过 膜,电解后,阴极室中
中铜离子得到电子后析出铜,CNl皮析出并富集,电解阴极室 储槽中err含量高时将其转移到电渗析淡水储槽,再进电渗析淡水室,在电渗析淡水室err离 子被转移并浓缩到电渗析浓水室,而
等络离子不能被通过膜,仍留在电渗析淡水 室,电渗析淡水储槽中的err离子浓度较低时,再将其返回电解阴极室储槽,再电解
析出金属铜和CN^电渗析淡水储槽中的CN'
离子浓度都较低时,将其转 入电渗析浓水储槽作为电渗析浓水。当电渗析浓水储槽中的CN-浓度较高时将其送回银浸 出工序,用于银的提取。
[0008] 前面所述的方法,优选的方案是,电解阴极室储槽和电渗析淡水储槽合而为一。
[0009] 前面所述的方法,优选的方案是,电渗析浓水储槽预装纯水。
[0010] 前面所述的方法,优选的方案是,电渗析浓水储槽预装经过电解和电渗析后除去 了铜锌和氰根的淡水。
[0011] 前面所述的方法,优选的方案是,电渗析极水储槽碱、硫酸钠、硫酸钾、硝酸钠、硝 酸钾难电解的稳定性盐的水溶液做极水。
[0012] 前面所述的方法,优选的方案是,在阳极室加入碱、硫酸钠、硫酸钾、硝酸钠、硝酸 钾难电解的稳定性盐的水溶液做阳极液。
[0013] 前面所述的方法,优选的方案是,阳极室中碱、盐的浓度为0.01 -15 %,优选0.5- 3%〇
[0014] 前面所述的方法,优选的方案是,用冷冻结晶的方法除去硫酸钠。
附图说明
[0015] 图1是脱铜分氰联立工艺处理银冶炼含氰贫液的工艺及装置结构示意图。其中1-含氰贫液补入;2-电解阴极室储槽;3-电解阴极;4-阳离子交换膜;5-电解阳极;6-电解阴极 室;7-电解阳极室;8-电解阳极室储槽;9-电渗析阳极室盐或碱补充;10-铜锌采出;11-电渗 析淡水储槽;12-电渗析极水储槽;13-电渗析浓水储槽;14-电渗析极板;15-电渗析阴阳离 子交换膜;16-含氰贫液回用或去脱硝工序;17-去电渗析浓水储槽。
[0016] 具体实施方法
[0017] 下面结合实施例详细说明本发明的技术方案,但保护范围不限于此。本发明所用 装置皆可从市场购买。
[0018] 实施例1:
[0019] 根据分析,含氰循环贫液中对银提取影响最大的杂质是铜,铜能在矿物表面形成 致密膜,影响银的提取,而铜与溶液中的Cf形成
,非常稳定难以除去,现有的方法 是先酸化,将HCN吹除,形成硫氰酸亚铜沉淀而除去。文献(胡湖生等,电积一酸化法从高铜 氰溶液中回收铜氰锌,有色金属,2000,52 (3) : 61-65)提出的方法是先酸化吹除HCN,再对沉 淀进行萃取得到高浓度含铜溶液,然后在回来电解,这一过程非常复杂,危险性大,成本高。
[0020] 如果直接对含氰贫液电解沉积铜锌,电解过程中除了使铜锌析出外还产生了游离 CN'Cf不断增多,铜、锌在阴极表面过电位增加,析出的出的量会大于铜和锌,于是阴极电 积电流效率逐渐下降,当Cf到一定浓度后只析出H2,不析出铜、锌,电解过程只是在做无用 功。例如,当CN—浓度17800mg/L,Cu浓度5000mg/L,Zn浓度5000mg/L的含氰贫液电解16小时 后,浓度变为:CN—浓度25707mg/L,Cu浓度3766mg/L,Zn浓度3268mg/L,说明电解后Cu、Zn析 出,游离Cf增加,但如果再继续电解10小时,CN'Cu、Zn浓度则不再发生变化,这说明阴极已 不能析出Cu和Zn,而主要是析出H2。因此,要保证阴极效率,必须将Cr分离出去。
[0021] 为解决这个问题,文献(王庆生,胺萃取电积法从含氰废液中回收铜锌半工业试 验,环境科学研究,1999,1 (2) :46-49)采用萃取的方法将Cu和Zn萃取出来,与CN_分离并浓 缩后,再去电解,但这种方法操作复杂,废弃的萃取剂又产生环境问题,因此,并没有得到广 泛应用。
[0022] 电解时,阴极液为待处理的含氰贫液,阴极发生的主要反应:
[0025] 如果游离Cf浓度高,则主要发生如下反应:
[0026] 2H++2e = H2
[0027] 本专利申请采用电渗析的方法除去游离方法,
[0028] 为解决此问题,本发明提出了脱铜分氰联立工艺处理银冶炼含氰贫液的新方法, 在脱除铜和锌的同时分离氰根,防止电解出来的氰根在阴极的积累,即在电解的同时加电 渗析操作,及时将游离err除去,保证阴极电解(或者电积)的效率。
[0029] 本工艺的核心是实现同时脱铜和分氰,采用的原理是利用电解将
等络离 子电解,铜和锌等金属析出,而err游离出来,游离出来的Cf体积小,可以通过阴离子交换 膜,而
虽然也是阴离子,但不能通过离子交换膜,因此可以通过电渗析实现
与CPT的分尚。
[0030] 图1是脱铜分氰联立工艺处理银冶炼含氰贫液的工艺及装置结构示意图。参考附 图1,本发明的关键在于同时脱铜和分氰,为了实现这一目的,将电解与电渗析联合操作,含 氰贫液⑴预先加入电解阴极室储罐(2),再进电解阴极室(6),含碱或盐的阳极溶液预先存 于电解阳极室储槽(8),再进电解槽的阳极室(7),电解槽阴极和阳极之间加阳离子交换膜 (4),可以允许阳极室中的阳离子Na+通过膜进入阴极室,实现电路回路的联通,但阴极室电 解产生的阴离子err不能通过膜进入阳极室,防止err在阳极被氧化。经过电解,阴极室中
等络离子中铜和锌等重金属离子得到电子后析出铜或锌,CN_&被析出并富集,当 电解阴极室储槽(2)中Cf含量较高时将其转移到电渗析淡水储槽(11)。
[0031] 转移到电渗析淡水储槽(11)的电解液富集了Cr,但仍含有
等络离子,直 接回用于金银提取会影响提取率,为实现这两种离子的分离,电渗析淡水储槽(11)的溶液 再进电渗析淡水室,在电渗析中离子被转移并浓缩到电渗析浓水室,而^
等络离 子不能被通过膜,仍留在电渗析淡水室,当电渗析淡水储槽中(11)的err离子浓度较低时, 再将其返回电解阴极室储槽(2),再电解
析出金属铜和CN^电解阴极室储槽(2)和 电渗析的淡水储槽(11)也可以合而为一。当电渗析淡水储槽(11)中的CN_
等离子 浓度都较低时可以转入电渗析浓水储槽(13)作为电渗析浓水。当电渗析浓水储槽(13)中的 Cf浓度较高时将其送回银浸出工序(16),用于银的提取。
[0032] 电渗析浓水储槽(13)可以预装纯水,或者电渗析淡水储槽(11)中经过电解和电渗 析后除去了铜锌和氰根的淡水。
[0033] 电渗析极水储槽(12)也预加碱或盐的水溶液。
[0034] 阳极室加入碱、硫酸钠、硫酸钾、硝酸钠、硝酸钾等难电解的稳定性盐的水溶液做 阳极液,阳极室中的Na+或K+在电场驱动下通过离子交换膜进入氰化物回收室,完成电流的 通路,并与阴极室释放的Cf结合为NaCN或KCN回用于银的提取。阳极室中碱或者难电解盐 的浓度为0.01-15%,优选0.5-3%。
[0035] 电解时阳极液采用含硫氰酸钠、NaOH或者难电解的盐类的水溶液,阳极发生的主 要反应:
[0036] 40H—-4e = 〇2+2H20
[0037] 采用硫氰酸钠为阳极液时,硫氰酸根可以被氧化为氰根,可以作为金银冶炼的原 料。
[0038] 当含氰贫液中含较多硫酸钠时,可采用冷冻结晶脱硝的方法将硫酸钠除去,硫酸 钠的溶解度与温度关系密切,温度为〇 °C和30°C的溶解度分别为4.9g和40.8g,通过冷冻结 晶除去硫酸钠,可以防止冬季管道堵塞,此方法为化工生产常规方法。
[0039] 本发明带离子交换膜的电解槽如附图所示,电解部分离子交换膜采用EDI离子交 换膜,500mmX 100mm,阳极室体积5L,阴极室体积5L,阳极用钛镀钌极板,阴极用铜板;电渗 析采用1级2段式,离子交换膜4对,膜面积320mmX IOOmm,采用EDI离子交换膜,阳极用钛镀 钌极板,阴极也用采用钛镀钌极板;采用某工业装置产生的含氰贫液为原料,组成见表1。
[0040] 表1含氰贫液组成
[0041]
[0042] 采用前述的离子交换膜电解槽电解,采用1 %的NaOH溶液为阳极液,电解:电压 5.2V,电流1.2A,电渗析:电压5V,电流0.6A,电解、电渗析同时进行7小时后,含氰贫液组成 见表2,可以达到回用于银冶炼的需要。
[0043] 表2电解阴极室储槽
[0044]
Claims (6)
1. 一种脱铜分氰联立工艺处理银冶炼含氰贫液的方法,其特征是,将电解与电渗析联 合操作,含氰贫液预先加入电解阴极室储槽,再进电解阴极室,含碱或盐的阳极溶液预先存 于电解阳极室储槽,再进电解槽的阳极室,电解槽阴极和阳极之间加阳离子交换膜,阳离子 通过膜进入阴极室,实现电路回路的联通,阴极室电解产生的阴离子不通过膜,电解后,阴 极室中
中铜离子得到电子后析出铜,CNl皮析出并富集,电解阴极室储槽中err含量 高时将其转移到电渗析淡水储槽,再进电渗析淡水室,在电渗析淡水室err离子被转移并浓 缩到电渗析浓水室,而
络离子不能被通过膜,仍留在电渗析淡水室,电渗析淡水储 槽中的err离子浓度较低时,再将其返回电解阴极室储槽,再电解
析出金属铜和 CN'电渗析淡水储槽中的CN'
离子浓度都较低时,将其转入电渗析浓水储槽作为 电渗析浓水,当电渗析浓水储槽中的Cf浓度较高时将其送回银浸出工序,用于银的提取, 电渗析极水储槽以碱、硫酸钠、硫酸钾、硝酸钠或硝酸钾难电解的稳定性盐的水溶液做极 水,在阳极室加入碱、硫酸钠、硫酸钾、硝酸钠或硝酸钾难电解的稳定性盐的水溶液做阳极 液,阳极室中碱、盐的浓度为O. OI-15%。
2. 根据权利要求1所述的方法,其特征是,电解阴极室储槽和电渗析淡水储槽合而为 〇
3. 根据权利要求1所述的方法,其特征是,电渗析浓水储槽预装纯水。
4. 根据权利要求1所述的方法,其特征是,电渗析浓水储槽预装经过电解和电渗析后除 去了铜锌和氰根的淡水。
5. 根据权利要求1所述的方法,其特征是,阳极室中碱、盐的浓度为0.5-3 %。
6. 根据权利要求1所述的方法,其特征是,用冷冻结晶的方法除去硫酸钠。
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