MX355250B - Metodo para la preparacion de cristales de nitrato de cobalto de alta pureza a partir de catalizadores residuales de co/sio2. - Google Patents

Metodo para la preparacion de cristales de nitrato de cobalto de alta pureza a partir de catalizadores residuales de co/sio2.

Info

Publication number
MX355250B
MX355250B MX2014010568A MX2014010568A MX355250B MX 355250 B MX355250 B MX 355250B MX 2014010568 A MX2014010568 A MX 2014010568A MX 2014010568 A MX2014010568 A MX 2014010568A MX 355250 B MX355250 B MX 355250B
Authority
MX
Mexico
Prior art keywords
solution
waste catalysts
cobalt nitrate
sio2
cobalt
Prior art date
Application number
MX2014010568A
Other languages
English (en)
Other versions
MX2014010568A (es
Inventor
Han Yiming
Liu Qianqian
Lai Bo
Xu Li
Song Dechen
Original Assignee
Wuhan Kaidi Eng Tech Res Inst
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 Wuhan Kaidi Eng Tech Res Inst filed Critical Wuhan Kaidi Eng Tech Res Inst
Publication of MX2014010568A publication Critical patent/MX2014010568A/es
Publication of MX355250B publication Critical patent/MX355250B/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B23/00Obtaining nickel or cobalt
    • C22B23/04Obtaining nickel or cobalt by wet processes
    • C22B23/0407Leaching processes
    • C22B23/0415Leaching processes with acids or salt solutions except ammonium salts solutions
    • C22B23/0438Nitric acids or salts thereof
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G51/00Compounds of cobalt
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G51/00Compounds of cobalt
    • C01G51/04Oxides; Hydroxides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • C07C51/412Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B1/00Preliminary treatment of ores or scrap
    • C22B1/005Preliminary treatment of scrap
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B7/00Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
    • C22B7/009General processes for recovering metals or metallic compounds from spent catalysts
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/80Compositional purity
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B3/00Extraction of metal compounds from ores or concentrates by wet processes
    • C22B3/20Treatment or purification of solutions, e.g. obtained by leaching
    • C22B3/26Treatment or purification of solutions, e.g. obtained by leaching by liquid-liquid extraction using organic compounds
    • C22B3/32Carboxylic acids
    • C22B3/322Oxalic acids
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Metallurgy (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Geology (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Catalysts (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)
  • Processing Of Solid Wastes (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Removal Of Specific Substances (AREA)

Abstract

Se proporciona un método para la preparación cristales de nitrato de cobalto de alta pureza a partir de catalizador residual de Co/SiO2. El método comprende secuencialmente las siguientes etapas: 1) calcinar el catalizador residual de Co/SiO2 siendo tratado a 350 a 500°C en presencia de aire durante 3 a 6 horas, moler el catalizador residual de Co/SiO2 como polvo después de enfriarlo a temperatura ambiente; 2) transferir el catalizador residual en polvo a un reactor de lecho fluidizado, tomando la reacción de reducción de 8 a 12 horas en una mezcla de gas de H2 y N2 3) añadir el catalizador residual después de la reacción de reducción a una solución de ácido nítrico muy diluida hasta disolverse completamente y filtrar; 4) utilizar un líquido alcalino para regular el pH de la solución de nitrato de cobalto obtenida, a un valor de 1.5, añadir una solución de ácido oxálico para que reaccione, en un baño de agua entre 25 a 80°C, regular el pH de la solución de reacción a un valor de 1.5 con una solución alcalina diluida y filtrar la solución caliente para obtener un precipitado de oxalato de cobalto; 5) después de secar el precipitado de oxalato de cobalto, calcinar el precipitado de oxalato de cobalto secó a una temperatura de 550 a 650°C durante 4 a 8 horas; 6) disolver el óxido de cobalto obtenido en una solución de ácido nítrico diluido y 7) evaporar y cristalizar la solución de nitrato de cobalto para obtener cristales de Co(NO3)2 · 6H2O. La tasa de recuperación y la pureza del Co(NO3)2 · 6H2O del método son elevadas.
MX2014010568A 2012-03-05 2013-03-04 Metodo para la preparacion de cristales de nitrato de cobalto de alta pureza a partir de catalizadores residuales de co/sio2. MX355250B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201210055799.5A CN102583580B (zh) 2012-03-05 2012-03-05 利用Co/SiO2废催化剂制备高纯硝酸钴晶体的方法
PCT/CN2013/072109 WO2013131452A1 (zh) 2012-03-05 2013-03-04 利用Co/SiO2废催化剂制备高纯硝酸钴晶体的方法

Publications (2)

Publication Number Publication Date
MX2014010568A MX2014010568A (es) 2014-12-08
MX355250B true MX355250B (es) 2018-04-11

Family

ID=46472943

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2014010568A MX355250B (es) 2012-03-05 2013-03-04 Metodo para la preparacion de cristales de nitrato de cobalto de alta pureza a partir de catalizadores residuales de co/sio2.

Country Status (20)

Country Link
US (1) US8986644B2 (es)
EP (1) EP2824075B1 (es)
JP (1) JP5837998B2 (es)
KR (1) KR101567589B1 (es)
CN (1) CN102583580B (es)
AP (1) AP2014007987A0 (es)
AU (1) AU2013230404B2 (es)
BR (1) BR112014021849B1 (es)
CA (1) CA2866188C (es)
DK (1) DK2824075T3 (es)
HR (1) HRP20171983T1 (es)
HU (1) HUE036070T2 (es)
IN (1) IN2014MN01922A (es)
MX (1) MX355250B (es)
MY (1) MY157636A (es)
RU (1) RU2580744C1 (es)
SG (1) SG11201405384YA (es)
SI (1) SI2824075T1 (es)
WO (1) WO2013131452A1 (es)
ZA (1) ZA201407150B (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105543496B (zh) * 2015-12-29 2017-10-20 武汉凯迪工程技术研究总院有限公司 费托合成废催化剂Co‑Rh/Al2O3中金属钴、铑和铝的回收方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1125781C (zh) * 2001-11-13 2003-10-29 山东大学 四氧化三钴纳米粉体的制备方法
US7285188B2 (en) * 2001-12-21 2007-10-23 Georgia Tech Research Corporation Oxynitride compounds, methods of preparation, and uses thereof
CN1190266C (zh) * 2002-08-19 2005-02-23 中国科学院山西煤炭化学研究所 一种用于费托合成的含钴废催化剂的回收方法
EP1827685A1 (en) * 2004-12-23 2007-09-05 Shell Internationale Research Maatschappij B.V. Method of preparing catalyst support from a waste catalyst
WO2008139407A2 (en) * 2007-05-11 2008-11-20 Sasol Technology (Proprietary) Limited Catalysts
CN101270420A (zh) * 2008-05-19 2008-09-24 中国科学院山西煤炭化学研究所 一种钴基费托合成催化剂中钴的回收方法
CN101698152A (zh) * 2009-10-20 2010-04-28 武汉凯迪科技发展研究院有限公司 一种钴基费托合成催化剂及其制备方法和应用
CN101700913B (zh) * 2009-11-17 2011-05-18 中南民族大学 利用费托合成用氧化铝负载钴基废催化剂制备高纯硝酸钴
CN102796873B (zh) * 2012-03-05 2014-02-26 阳光凯迪新能源集团有限公司 从费托合成废催化剂Co-Ru/Al2O3中综合回收金属钴、钌和铝的方法

Also Published As

Publication number Publication date
AP2014007987A0 (en) 2014-10-31
US8986644B2 (en) 2015-03-24
JP2015515362A (ja) 2015-05-28
US20140377153A1 (en) 2014-12-25
CN102583580A (zh) 2012-07-18
KR20140130748A (ko) 2014-11-11
SI2824075T1 (en) 2018-05-31
EP2824075B1 (en) 2017-10-11
SG11201405384YA (en) 2014-10-30
BR112014021849B1 (pt) 2020-12-15
DK2824075T3 (en) 2018-01-15
IN2014MN01922A (es) 2015-07-10
EP2824075A4 (en) 2015-11-18
AU2013230404B2 (en) 2015-02-19
CA2866188A1 (en) 2013-09-12
ZA201407150B (en) 2015-11-25
MX2014010568A (es) 2014-12-08
CN102583580B (zh) 2014-03-12
HUE036070T2 (hu) 2018-06-28
WO2013131452A1 (zh) 2013-09-12
AU2013230404A1 (en) 2014-10-16
EP2824075A1 (en) 2015-01-14
HRP20171983T1 (hr) 2018-02-23
CA2866188C (en) 2017-04-18
MY157636A (en) 2016-07-15
RU2580744C1 (ru) 2016-04-10
JP5837998B2 (ja) 2015-12-24
KR101567589B1 (ko) 2015-11-09

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