CN1161935A - Method for production of silver potassium cyanide - Google Patents

Method for production of silver potassium cyanide Download PDF

Info

Publication number
CN1161935A
CN1161935A CN 96103774 CN96103774A CN1161935A CN 1161935 A CN1161935 A CN 1161935A CN 96103774 CN96103774 CN 96103774 CN 96103774 A CN96103774 A CN 96103774A CN 1161935 A CN1161935 A CN 1161935A
Authority
CN
China
Prior art keywords
silver
potassium cyanide
cyanide
solution
production
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
CN 96103774
Other languages
Chinese (zh)
Inventor
刘长让
卢月梅
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.)
Zhengzhou University
Original Assignee
Zhengzhou University
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 Zhengzhou University filed Critical Zhengzhou University
Priority to CN 96103774 priority Critical patent/CN1161935A/en
Publication of CN1161935A publication Critical patent/CN1161935A/en
Pending legal-status Critical Current

Links

Landscapes

  • Battery Electrode And Active Subsutance (AREA)

Abstract

A new method for production of potassium argentocyanide is to use the basic material or base-releasing materiol to neutralize silver nitrate solution, then the neutrolizes silver nitrate solution is added to potassium cyanide solution to directly precipitate silver cyanide, and finally, silver cyanide reacts again with potassium cyanide to obtain potassium argentocyanide. As compared with the existing method, this invention does not pass through such procedures of evaporation, cooling, crystallization, drying, etc., greatly shortens the flow-path, and raises the economic benefit.

Description

A kind of novel method of producing silver potassium cyanide.
The present invention relates to the production method of silver potassium cyanide.
Japanese publication " method that mineral compound prepares the production silver potassium cyanide of introducing in the handbook (the 3rd volume) is the production method that adopts usually at present, that is: with 1: 1 nitric acid dissolve argent, the silver nitrate solution that obtains is evaporated to remove excessive nitric acid, obtain the Silver Nitrate crystallization after the cooling, after filtration after the oven dry, press Silver Nitrate and 1: 1 mol ratio of potassium cyanide by calculating, be made into Silver Nitrate and potassium cyanide solution that concentration is 1mol/L respectively, under agitation Silver Nitrate is joined and be settled out silver cyanide in the potassium cyanide solution, then silver cyanide is made silver potassium cyanide with potassium cyanide by 1: 1 molar ratio reaction again.The whole process of this production method comprises dissolving, evaporation, cooling, crystallization, filtration, oven dry, dissolving again, steps such as precipitation, reaction, and it is long to exist operational path, complex operation, energy consumption height, the high deficiency of production cost.
The purpose of this invention is to provide a kind of novel method of simpler and more direct production silver potassium cyanide,, reduce cost so that shorten operational path greatly.
Technical scheme of the present invention is: silver is put into 1: 1 nitric acid be dissolved into silver nitrate solution, limit stirring silver nitrate solution limit progressively adds alkaline matter or releases alkaloid substance then, makes its certain pH value that neutralizes; Above-mentioned Silver Nitrate neutralizer is slowly joined in the potassium cyanide solution of equimolar amount, stir simultaneously, be settled out silver cyanide, again the silver cyanide that obtains and the potassium cyanide solution of equimolar amount are reacted under 50~95 ℃ of temperature, promptly make silver potassium cyanide solution.Wherein employed alkaline matter or release alkaloid substance preferably ammoniacal liquor or urea or bicarbonate of ammonia is between the pH value control 5-8 of Silver Nitrate neutralizer.
The present invention do not compare with existing production method need evaporate, cooling, crystallization, filtration, oven dry, process such as dissolving again, shortened technical process greatly, reduced energy consumption, reduced production cost, obviously improved productivity effect.
Below be embodiments of the invention:
Get purity and be 99.95% argent 54g (0.5mol) and place reaction vessel, add 10% sodium hydroxide solution, be heated to 80-90 ℃, remove degreasing, wash down with deionized water then.With 80ml1: 1 analytical pure nitric acid joins in the reaction vessel that is placed with silver, (heating for dissolving in case of necessity), treat that silver dissolves fully after, being diluted to volume with deionized water is 500ml; Under violent stirring, splash into the ammoniacal liquor of 2mol/L or urea or bicarbonate of ammonia then gradually and neutralize, monitor pH value with acidometer simultaneously, when pH value reaches between the 5-8, stop to add ammoniacal liquor (or urea or carbonic acid cyanogen ammonium).In another container, 33g (0.5mol) potassium cyanide is dissolved as 500ml solution; Under agitation above-mentioned Silver Nitrate neutralizer is slowly poured in the potassium cyanide solution with the thread shape, generated white fine-grannular precipitation, through suction filtration, deionized water wash is dried under 80-90 ℃ of temperature, obtains silver cyanide 66.5g (productive rate 99.4%).Silver cyanide is joined in the 500ml solution that contains 0.5mol potassium cyanide at last again, under 50~95 ℃ of temperature, react, just make silver potassium cyanide.

Claims (3)

1, a kind of production silver potassium cyanide novel method is characterized in that:
(1) nitric acid of silver being put into 1: 1 dissolves and becomes silver nitrate solution;
(2) silver nitrate solution is stirred on the limit, and the limit adds alkaline matter gradually or releases alkaloid substance, makes its certain pH value that neutralizes;
(3) above-mentioned Silver Nitrate neutralizer is slowly joined in the potassium cyanide solution of equimolar amount, stir simultaneously, be settled out silver cyanide;
(4) again the potassium cyanide solution of above-mentioned silver cyanide that obtains and equimolar amount is reacted under 50~95 ℃ of temperature, promptly make silver potassium cyanide.
2,, it is characterized in that described alkaline matter or release alkaloid substance preferably ammoniacal liquor or urea or bicarbonate of ammonia according to the novel method of the described production silver potassium cyanide of claim 1.
3, according to the novel method of the described production silver potassium cyanide of claim 1, its feature is controlled between the 5-8 at the pH value of the described neutralizer of fourth.
CN 96103774 1996-04-11 1996-04-11 Method for production of silver potassium cyanide Pending CN1161935A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 96103774 CN1161935A (en) 1996-04-11 1996-04-11 Method for production of silver potassium cyanide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 96103774 CN1161935A (en) 1996-04-11 1996-04-11 Method for production of silver potassium cyanide

Publications (1)

Publication Number Publication Date
CN1161935A true CN1161935A (en) 1997-10-15

Family

ID=5118196

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 96103774 Pending CN1161935A (en) 1996-04-11 1996-04-11 Method for production of silver potassium cyanide

Country Status (1)

Country Link
CN (1) CN1161935A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102874844A (en) * 2012-10-25 2013-01-16 河南银城科技股份有限公司 Method for producing silver potassium cyanide
CN104250012A (en) * 2014-09-27 2014-12-31 深圳市鑫鸿发环保设备有限公司 Silver cyanide manufacturing technology and equipment thereof
CN113247919A (en) * 2021-05-21 2021-08-13 漯河瀚普环创环保科技有限公司 Preparation method of silver potassium cyanide

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102874844A (en) * 2012-10-25 2013-01-16 河南银城科技股份有限公司 Method for producing silver potassium cyanide
CN104250012A (en) * 2014-09-27 2014-12-31 深圳市鑫鸿发环保设备有限公司 Silver cyanide manufacturing technology and equipment thereof
CN113247919A (en) * 2021-05-21 2021-08-13 漯河瀚普环创环保科技有限公司 Preparation method of silver potassium cyanide

Similar Documents

Publication Publication Date Title
CN100488937C (en) Production method of ferrous oxalate special for ferrous lithium phosphate
CN101748297A (en) Method for preparing ammonium metavanadate from vanadium extraction leaching solution
CN103214388B (en) A kind of recoverying and utilizing method of nitrating wasting acid
CN104944400A (en) Technology for preparing iron phosphate through hydrolytic method
CN101643236A (en) Production of zinc oxide by ammonia water circulation method
CN101049915A (en) Method for comprehensive using tail gas of rotary kiln and dilute sulfuric acid in procedure of producing white titanium pigment through sulfuric acid method
CN113968578B (en) Method for synthesizing ferric phosphate by using titanium dioxide byproduct ferrous sulfate
CN102531055B (en) The preparation method of sodium metavanadate/potassium metavanadate
CN1161935A (en) Method for production of silver potassium cyanide
WO2023246156A1 (en) Process for preparing lithium hydroxide by causticization and use thereof
US4044106A (en) Reclamation of phosphate from bright dip drag-out
CN107265425A (en) The method that lithium phosphate is prepared using pelite containing lithium
CN101891235A (en) Method for preparing high-grade pure ceric sulfate
CN105271406B (en) A kind of preparation method of sodium metavanadate
CN115893749A (en) Resource utilization method for lithium battery anode ternary precursor production wastewater
CA1140730A (en) Process for producing magnesium oxide from an aqueous magnesium sulphate solution
CN1044222C (en) Method for comprehensive utilization of sodium sulfate containing chromium
CN1077753A (en) Active zinc flower and high-purity zinc oxide preparation technology
CN114702075A (en) Purification preparation method of manganese sulfate
CN112340912A (en) Method for recovering inorganic salt in ammonia desulphurization waste liquid
CN1091112A (en) Preparation of potassium sulfate by circulating double decomposition of ammonium sulfate and potassium chloride
JP2550575B2 (en) Recovery method of ammonium thiocyanate
CN102020293A (en) Method for recovering reagent grade sodium nitrate from waste liquid generated in citric acid bismuth production
CN105236483B (en) A kind of preparation method of potassium metavanadate
CN109319752A (en) A kind of preparation method of hydrazine sulfate

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C01 Deemed withdrawal of patent application (patent law 1993)
WD01 Invention patent application deemed withdrawn after publication