CN108655415A - A kind of new process preparing high-purity platinum - Google Patents

A kind of new process preparing high-purity platinum Download PDF

Info

Publication number
CN108655415A
CN108655415A CN201810636388.2A CN201810636388A CN108655415A CN 108655415 A CN108655415 A CN 108655415A CN 201810636388 A CN201810636388 A CN 201810636388A CN 108655415 A CN108655415 A CN 108655415A
Authority
CN
China
Prior art keywords
platinum
purity
preparing high
new process
added
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
CN201810636388.2A
Other languages
Chinese (zh)
Inventor
姚志刚
王健
李忠飞
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.)
NANJING DONGRUI PLATINUM Co Ltd
Original Assignee
NANJING DONGRUI PLATINUM 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 NANJING DONGRUI PLATINUM Co Ltd filed Critical NANJING DONGRUI PLATINUM Co Ltd
Priority to CN201810636388.2A priority Critical patent/CN108655415A/en
Publication of CN108655415A publication Critical patent/CN108655415A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00Making metallic powder or suspensions thereof
    • B22F9/16Making metallic powder or suspensions thereof using chemical processes
    • B22F9/18Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds
    • B22F9/24Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B11/00Obtaining noble metals
    • C22B11/04Obtaining noble metals by wet processes

Abstract

The present invention relates to a kind of new processes preparing high-purity platinum, and high-purity platinum powder is arrived using the new method system of hydrochloric acid+dioxygen water dissolution, chlorination ammonia-sinking platinum, combining hydrogen oxidation sodium dissolving+hydrazine hydrate reduction.The present invention uses the dissolving method of hydrochloric acid+hydrogen peroxide, does not bring impurity into, need not catch up with nitre, simplifies technique, substantially reduces energy consumption, reduces enterprise's production cost, and environmental protection.The method that the secondary dissolving of the present invention uses alkali soluble, it is shorter much than traditional aqua regia dissolution reaction time, and nitre need not be caught up with, simplify technique, substantially reduce energy consumption, reduces enterprise's production cost, and environmental protection.

Description

A kind of new process preparing high-purity platinum
Technical field
The present invention relates to a kind of Chemical Decomposition methods, and in particular to a kind of new process preparing high-purity platinum.
Background technology
There are many method of refining of platinum, and summing up has chlorination carbonyl platinum method, fused salt electrolysis process, zone melting method, chlorination Ammonium repeated precipitation process, sodium bromate Hydrolyze method, oxidation carrier Hydrolyze method etc..Wherein chlorination carbonyl process, fused salt electrolysis process are due to technique Process is complicated, cumbersome, its large-scale production and application is made to be restricted.Zone melting method mainly for the production of ultra-pure platinum, The also seldom application in large-scale industrial production.Sodium bromate Hydrolyze method, oxidation carrier Hydrolyze method solution treatment amount are big and need Supernatant is stood for a long time, and occupied space place, the production cycle is long, can not also be mass produced.Existing recovery process labor Fatigue resistance is big, low production efficiency, inconvenient, high energy consumption.
Invention content
The purpose of the present invention is being directed to above-mentioned production technology, using hydrochloric acid+dioxygen water dissolution, chlorination ammonia-sinking platinum, The new method system of combining hydrogen oxidation sodium dissolving+hydrazine hydrate reduction arrives high-purity platinum powder.
To achieve the above object, technical solution provided by the invention is:
A kind of new process preparing high-purity platinum, it is characterised in that:Include the following steps:
1) levigate:It is levigate that platiniferous material is put into ball mill, is cooled to room temperature, obtains the waste material of minus 200 mesh granularity;
2) acid is molten:According to reactor capacity size, weighs suitable raw material and the salt acid soak of 3~4mol/L is added, add 30% hydrogen peroxide solution is added dropwise to 75 DEG C~85 DEG C of temperature in heat, until having dissolved, filters off insoluble matter.
3) it precipitates:The ammonium chloride that 1~1.5 times of weight of platinum is added carries out heavy platinum, stands and is cooled to room temperature after the completion of precipitation, Ammonium chloroplatinate is filtered, washed;
4) alkali soluble:Solid sodium hydroxide is added portionwise under stirring, until be completely dissolved, static 10~after twenty minutes Filter off insoluble matter;
5) it restores:Hydrazine hydrate reduction is added after lysate is heated to 50~60 DEG C and goes out platinum;
6) platinum powder after reduction is filtered, washed, dried.
In step 1), 2000 turns/hour of drum's speed of rotation, Ball-milling Time 30~40 minutes.
In step 5), the reaction time is 0.5~1 hour.
The platinum powder purity of production reaches 99.9995%.
Compared with prior art, the beneficial effects of the invention are as follows:
The present invention is first levigate by material so that increases contact area when dissolving, improves solution rate.The present invention uses hydrochloric acid The dissolving method of+hydrogen peroxide, does not bring impurity into, need not catch up with nitre, simplifies technique, substantially reduces energy consumption, reduces enterprise and is produced into This, and environmental protection.The method that the secondary dissolving of the present invention uses alkali soluble, it is shorter much than traditional aqua regia dissolution reaction time, and be not required to Nitre is caught up with, technique is simplified, substantially reduces energy consumption, reduces enterprise's production cost, and environmental protection.
Thus the platinum powder purity of technique productions reaches 99.9995%, is existing market highest level.The product is for manufacturing Labware (crucible, electrode, thermocouple, resistance wire etc.), industrial catalyst, high-precision electronic product, pharmaceuticals industry are for making Make various antitumor drugs etc..
Specific implementation mode
The present invention is further explained in the light of specific embodiments.
1, levigate.It is levigate that platiniferous material is put into ball mill, is kept for 2000 turns/hour of machine rotational speed, 30~after forty minutes It shuts down, is cooled to room temperature, produces the waste material for obtaining minus 200 mesh granularity.
2, acid is molten.According to reactor capacity size, weighs suitable raw material and the salt acid soak of 3~4mol/L is added, add 30% hydrogen peroxide solution is added dropwise to 75 DEG C~85 DEG C of temperature in heat, until having dissolved.Filter off insoluble matter.
3, it precipitates.The ammonium chloride that 1~1.5 times of weight of platinum is added carries out heavy platinum, stands and is cooled to room temperature after the completion of precipitation, Ammonium chloroplatinate is filtered, washed.
4, alkali soluble.Solid sodium hydroxide is added portionwise under stirring, until be completely dissolved, static 10~after twenty minutes Filter off insoluble matter.
5, hydrazine hydrate reduction is added after lysate being heated to 50~60 degree and goes out platinum, the reaction time is 0.5~1 hour.
6, the platinum powder after reduction is filtered, washed, dried.
Platinum powder obtained is sent to national non-ferrous metal and the detection of electronic material Institute of Analysis, according to relevant criterion, Platinum powder purity is measured using glow discharge spectrometry and reaches 99.9995%.
The above is only presently preferred embodiments of the present invention, is not intended to limit the present invention in any form, any ripe Professional and technical personnel is known, without departing from the scope of the present invention, according to the technical essence of the invention, to above real Apply any simple modification, equivalent replacement and improvement etc. made by example, still fall within technical solution of the present invention protection domain it It is interior.

Claims (4)

1. a kind of new process preparing high-purity platinum, it is characterised in that:Include the following steps:
1) levigate:It is levigate that platiniferous material is put into ball mill, is cooled to room temperature, obtains the waste material of minus 200 mesh granularity;
2) acid is molten:According to reactor capacity size, weighs suitable raw material and the salt acid soak of 3~4mol/L is added, be heated to 75 DEG C~85 DEG C of temperature, is added dropwise 30% hydrogen peroxide solution, until having dissolved, filters off insoluble matter.
3) it precipitates:The ammonium chloride that 1~1.5 times of weight of platinum is added carries out heavy platinum, stands and is cooled to room temperature after the completion of precipitation, by chlorine Platinic acid ammonium is filtered, washed;
4) alkali soluble:Solid sodium hydroxide is added portionwise under stirring, until be completely dissolved, static 10~filter off after twenty minutes Insoluble matter;
5) it restores:Hydrazine hydrate reduction is added after lysate is heated to 50~60 DEG C and goes out platinum;
6) platinum powder after reduction is filtered, washed, dried.
2. the new process according to claim 1 for preparing high-purity platinum, it is characterised in that:In step 1), drum's speed of rotation 2000 turns/hour, Ball-milling Time 30~40 minutes.
3. the new process according to claim 1 for preparing high-purity platinum, it is characterised in that:In step 5), the reaction time 0.5 ~1 hour.
4. the new process according to claim 1 for preparing high-purity platinum, it is characterised in that:The platinum powder purity of production reaches 99.9995%.
CN201810636388.2A 2018-06-20 2018-06-20 A kind of new process preparing high-purity platinum Pending CN108655415A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810636388.2A CN108655415A (en) 2018-06-20 2018-06-20 A kind of new process preparing high-purity platinum

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810636388.2A CN108655415A (en) 2018-06-20 2018-06-20 A kind of new process preparing high-purity platinum

Publications (1)

Publication Number Publication Date
CN108655415A true CN108655415A (en) 2018-10-16

Family

ID=63772181

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810636388.2A Pending CN108655415A (en) 2018-06-20 2018-06-20 A kind of new process preparing high-purity platinum

Country Status (1)

Country Link
CN (1) CN108655415A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110340377A (en) * 2018-11-05 2019-10-18 贵研铂业股份有限公司 A kind of method that Whote-wet method prepares high-purity platinum powder
CN110482618A (en) * 2019-08-13 2019-11-22 中船重工黄冈贵金属有限公司 A kind of synthetic method of no nitre chloroplatinic acid
CN111455191A (en) * 2020-04-02 2020-07-28 西安宏星电子浆料科技股份有限公司 High-purity spongy platinum and preparation method and application thereof
CN111534700A (en) * 2020-06-24 2020-08-14 广东金正龙科技有限公司 Method for recovering residual precious metals in platinum purification wastewater
CN112961986A (en) * 2021-02-06 2021-06-15 中海油(山西)贵金属有限公司 Method for recovering noble metal in platinum online recoverer
CN114619040A (en) * 2022-03-18 2022-06-14 昆明理工大学 Method for refining platinum and preparing platinum black

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1370845A (en) * 2001-10-09 2002-09-25 金川集团有限公司 Refined platinum producing process
US7044995B2 (en) * 2002-11-13 2006-05-16 Pgm Refining Inc. Purification of metals from mixtures thereof
CN104745836A (en) * 2015-04-21 2015-07-01 昆山鸿福泰环保科技有限公司 Platinum recovery refining process
CN104831071A (en) * 2015-04-08 2015-08-12 昆明理工大学 Method for recovering platinum and palladium from waste carrier catalyst by hydrothermal method
CN107150128A (en) * 2017-05-12 2017-09-12 江西铜业集团公司 A kind of preparation method of high-purity platinum powder
CN107838434A (en) * 2017-10-30 2018-03-27 贵研铂业股份有限公司 A kind of preparation method of high-purity platinum powder

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1370845A (en) * 2001-10-09 2002-09-25 金川集团有限公司 Refined platinum producing process
US7044995B2 (en) * 2002-11-13 2006-05-16 Pgm Refining Inc. Purification of metals from mixtures thereof
CN104831071A (en) * 2015-04-08 2015-08-12 昆明理工大学 Method for recovering platinum and palladium from waste carrier catalyst by hydrothermal method
CN104745836A (en) * 2015-04-21 2015-07-01 昆山鸿福泰环保科技有限公司 Platinum recovery refining process
CN107150128A (en) * 2017-05-12 2017-09-12 江西铜业集团公司 A kind of preparation method of high-purity platinum powder
CN107838434A (en) * 2017-10-30 2018-03-27 贵研铂业股份有限公司 A kind of preparation method of high-purity platinum powder

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
王金利等: "国内废催化剂中铂的回收及提纯技术", 《化学工业与工程技术》 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110340377A (en) * 2018-11-05 2019-10-18 贵研铂业股份有限公司 A kind of method that Whote-wet method prepares high-purity platinum powder
CN110482618A (en) * 2019-08-13 2019-11-22 中船重工黄冈贵金属有限公司 A kind of synthetic method of no nitre chloroplatinic acid
CN111455191A (en) * 2020-04-02 2020-07-28 西安宏星电子浆料科技股份有限公司 High-purity spongy platinum and preparation method and application thereof
CN111455191B (en) * 2020-04-02 2022-03-01 西安宏星电子浆料科技股份有限公司 High-purity spongy platinum and preparation method and application thereof
CN111534700A (en) * 2020-06-24 2020-08-14 广东金正龙科技有限公司 Method for recovering residual precious metals in platinum purification wastewater
CN112961986A (en) * 2021-02-06 2021-06-15 中海油(山西)贵金属有限公司 Method for recovering noble metal in platinum online recoverer
CN114619040A (en) * 2022-03-18 2022-06-14 昆明理工大学 Method for refining platinum and preparing platinum black
CN114619040B (en) * 2022-03-18 2024-03-26 昆明理工大学 Method for refining platinum and preparing platinum black

Similar Documents

Publication Publication Date Title
CN108655415A (en) A kind of new process preparing high-purity platinum
CN103484687B (en) Platinum refining technology
JP6011809B2 (en) Method for producing gold powder with high bulk density
CN111054933B (en) Method for preparing high-purity rhodium powder from platinum-rhodium waste
CN105905874A (en) Method of recycling tellurium from anode mud
CN104745836A (en) Platinum recovery refining process
CN109609783B (en) Method for efficiently separating and purifying palladium and rhodium from alloy sheet containing palladium and rhodium alloy
CN101942568A (en) Method for recovering noble metal from waste computer and fittings thereof
CN113278813A (en) Method for separating and purifying rhodium in impurity-containing rhodium solution
CN104017994A (en) Method for recovering gold and tin from gold-tin alloy scrap
CN101705378B (en) Method for comprehensively recovering valuable metals from complex alloys containing stibium, tellurium, indium, germanium and silver
CN105385854A (en) Method for recycling precious metal including gold, platinum and palladium in jewelry processing polishing powder
CN104060095A (en) Method of recovering palladium from palladium-loading aluminum oxide waste catalyst
CN108264100B (en) Efficient synthesis method of rhodium nitrate solution
CN105648232B (en) One kind uses I2The method that gold refining is carried out with KI
CN102586629A (en) Recycling preparation method for producing titanium sponge and co-producing potassium cryolite with potassium fluotitanate as intermediate raw material
CN101973575B (en) Join production method of metastannic acid and stannate
CN105481005A (en) Preparation method of reagent-grade stannous chloride dehydrate crystals
CN105838900B (en) One kind uses I2The method that gold refining is carried out with NaI
CN106256914B (en) Bromine-sodium bromide gold refining method
CN108658133B (en) Rapid dissolving method of insoluble metal iridium
CN107586966B (en) Method for quickly activating and dissolving insoluble noble metal
CN104495803A (en) Purification method of natural microcrystalline graphite
CN114350971B (en) Method for recovering rhodium from rhodium-containing ammonium chloroplatinate precipitation slag
CN102021340B (en) Deep impurity removal technology for coarse gold powder

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20181016

RJ01 Rejection of invention patent application after publication