CN107052362A - High-specific surface area ultrafine palladium powder and preparation method thereof - Google Patents

High-specific surface area ultrafine palladium powder and preparation method thereof Download PDF

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Publication number
CN107052362A
CN107052362A CN201710450372.8A CN201710450372A CN107052362A CN 107052362 A CN107052362 A CN 107052362A CN 201710450372 A CN201710450372 A CN 201710450372A CN 107052362 A CN107052362 A CN 107052362A
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China
Prior art keywords
solution
surface area
specific surface
palladium
palladium powder
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CN201710450372.8A
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Inventor
孙社稷
田发香
王要东
陆冬梅
王大林
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Xian Hongxing Electronic Paste Technology Co Ltd
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Xian Hongxing Electronic Paste Technology Co Ltd
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Priority to CN201710450372.8A priority Critical patent/CN107052362A/en
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    • 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
    • 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
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/05Metallic powder characterised by the size or surface area of the particles

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemically Coating (AREA)
  • Conductive Materials (AREA)

Abstract

It is an object of the invention to provide high-specific surface area ultrafine palladium powder and preparation method thereof, in the prior art, the technology for producing palladium powder is also relatively backward, and the preparation method research lifted particularly with palladium powder specific surface area is also fewer.The step of the present invention is into chlorine palladium acid solution by High Purity Palladium aqua regia dissolution;Then in chlorine palladium acid solution plus aqueous slkali adjustment system PH is 9~12, and add and dissolved PVP dispersant solutions and stir and control solution temperature;Reducing agent is configured to finite concentration and adds above-mentioned system, after charging is finished, continues to stir, obtains ultrafine palladium powder slurries;After after slurries clarification, supernatant liquor is drawn, deionized water washing, cyclic washing to electrical conductivity ﹤ 20us/cm, and vacuum drying is added, that is, is prepared into ultrafine palladium powder.Ultrafine palladium powder specific surface area height, the adsorption activity prepared is strong.

Description

High-specific surface area ultrafine palladium powder and preparation method thereof
Technical field
The invention belongs to high-molecular compound technical field, it is related to high-specific surface area ultrafine palladium powder and preparation method thereof.
Background technology
Ultrafine palladium powder is a kind of industrial chemicals, and because the mode of production is different, product quality is also each variant, and manufacturing cost has Costliness has cheap, and the influence that environment is produced also is not quite similar.Domestic electronics industry develops later, the research to electronic material Fall behind foreign countries' more than ten years, the especially research to palladium powder reports that seldom, the technology for producing palladium powder is also relatively backward, Domestic Palladium powder Source relies primarily on import.
With the development of electronic information industry, metal blending property polymer conductor slurry has obtained fast development, ultra-fine palladium Powder is in metal blending property conducting polymer slurry in improving the drought resisting material erosiveness of slurry and preventing silver ion migration Excellent performance so as to the performance requirement more and more higher of palladium powder in industrial production.Wherein because high-specific surface area ultrafine palladium powder is super Strong surface-active, adsorptivity and its excellent electrical property, industrially by largely as hydrogen purification material, thick film ink Conductive phase, catalyst, purifying vehicle exhaust material etc. are applied.Some preparation sides for ultrafine palladium powder are had in the prior art Method, but the preparation method research lifted for palladium powder specific surface area is also fewer.
The content of the invention
In view of this, it is a primary object of the present invention to provide high-specific surface area ultrafine palladium powder and preparation method thereof.
To reach above-mentioned purpose, the technical proposal of the invention is realized in this way:
The preparation method of high-specific surface area ultrafine palladium powder, it is characterised in that comprise the following steps:
(1)High Purity Palladium aqua regia dissolution is into chlorine palladium acid solution, and obtained solution is the first solution;
(2)Weigh polyvinylpyrrolidone and aqueous povidone solution is dissolved into deionized water, it is stand-by;In the first solution It is PH=9~12 to plant and add aqueous slkali adjustment system, then adds the aqueous povidone solution dissolved and stirs, Obtained solution is the second solution, and controls the temperature of the second solution;
(3)By reducing agent deionized water dissolved dilution, obtained solution is the 3rd solution, and the 3rd solution is slowly added into second Solution is reduced, after addition is finished, and is continued to stir 30 minutes, is obtained ultrafine palladium powder slurries;
(4)After after the clarification of ultrafine palladium powder slurries, supernatant liquor is drawn, deionized water washing, cyclic washing to electrical conductivity ﹤ is added 20us/cm, and vacuum drying, that is, the product obtained are ultrafine palladium powder.
The step(1)In be into chlorine palladium acid solution, to add deionized water adjustment solution dense by High Purity Palladium aqua regia dissolution Degree, solution concentration is calculated as 2.0%~4.0% using simple substance palladium.
The step(2)The consumption of middle polyvinylpyrrolidone is the 0.1%~0.5% of the mass parts of High Purity Palladium.
The step(2)In aqueous slkali be natrium carbonicum calcinatum or sodium hydroxide.
The step(2)The middle temperature for controlling the second solution is 30~50 DEG C.
The step(3)The reducing agent of middle selection is hydrazine hydrate, glucose.
The step(3)The middle adition process time that 3rd solution is slowly added to the second solution is 1~3min.
The step(4)Middle mode of washing washs for mashing.
The step(4)Middle vacuum drying is that 36~42h is dried under 80 DEG C of vacuum condition.
High-specific surface area ultrafine palladium powder made from the preparation method of described high-specific surface area ultrafine palladium powder.
Compared with prior art, beneficial effects of the present invention:
1. experimental provision, experimental condition and preparation process are simple, easy to operate, Product yields are high, with low cost, raw suitable for industry Production;
2. controllability is good, the ultrafine palladium powder specific surface area prepared is 10~80m2/ g, specific surface area is high, adsorption activity is strong, Particle diameter is 2~5um, moisture < 0.5%;
3. products application extensively, can be used as hydrogen purification material, the conductive phase of thick film ink, catalyst, purifying vehicle exhaust material.
The ultrafine palladium powder specific surface area prepared after drying is 10~80m2/ g, particle diameter is 2~5um. moisture < 0.5%.
Brief description of the drawings
Fig. 1 is the SEM figures for the high-specific surface area ultrafine palladium powder that the present invention is provided.
Embodiment
In order to make the purpose , technical scheme and advantage of the present invention be clearer, it is right below in conjunction with drawings and Examples The present invention is further elaborated.It should be appreciated that the specific embodiments described herein are merely illustrative of the present invention, and It is not used in the restriction present invention.
The present invention provides a kind of preparation method of high-specific surface area ultrafine palladium powder, comprises the following steps:
(1)High Purity Palladium aqua regia dissolution is into chlorine palladium acid solution, and obtained solution is the first solution;
(2)Weigh polyvinylpyrrolidone and aqueous povidone solution is dissolved into deionized water, it is stand-by;In the first solution It is PH=9~12 to plant and add aqueous slkali adjustment system, then adds the aqueous povidone solution dissolved and stirs, Obtained solution is the second solution, and controls the temperature of the second solution;Polyvinylpyrrolidone is PVP, main to play scattered make With.
(3)By reducing agent deionized water dissolved dilution, obtained solution is the 3rd solution, and the 3rd solution is slowly added to Second solution is reduced, after addition is finished, and is continued to stir 30 minutes, is obtained ultrafine palladium powder slurries;
(4)After after the clarification of ultrafine palladium powder slurries, supernatant liquor is drawn, deionized water washing, cyclic washing to electrical conductivity ﹤ is added 20us/cm, and vacuum drying, that is, the product obtained are ultrafine palladium powder.
The step(1)In be into chlorine palladium acid solution, to add deionized water adjustment solution dense by High Purity Palladium aqua regia dissolution Degree, solution concentration is calculated as 2.0%~4.0% using simple substance palladium.It is mainly dissolving High Purity Palladium using the purpose of chloroazotic acid, can also be direct Using finished product chlorine palladium acid solution, but it is more expensive.
The step(2)The consumption of middle polyvinylpyrrolidone is the 0.1%~0.5% of the mass parts of High Purity Palladium.
The step(2)In aqueous slkali be natrium carbonicum calcinatum or sodium hydroxide.
The step(2)The middle temperature for controlling the second solution is 30~50 DEG C.
The step(3)The reducing agent of middle selection is hydrazine hydrate, glucose.
The step(3)The middle adition process time that 3rd solution is slowly added to the second solution is 1~3min.Added Gas, heat can be produced in a short time soon to cause danger;Added the ultrafine palladium powder surface area generated slowly not high.
The step(4)Middle mode of washing washs for mashing.
The step(4)Middle vacuum drying is that 36~42h is dried under 80 DEG C of vacuum condition.
High-specific surface area ultrafine palladium powder made from the preparation method of described high-specific surface area ultrafine palladium powder.
Embodiment 1
(1)By 50g High Purity Palladiums with 480mL aqua regia dissolutions into chlorine palladium acid solution, adding deionized water makes cumulative volume be 2000ml, dense Spend for 2.4%(Calculated with simple substance palladium).
(2)The aqueous solution that 0.1gPVP is dissolved into 0.1% with deionized water is weighed, it is stand-by.(1)Middle addition 150ml concentration The alkaline solution that system is PH=11~12, water-bath are adjusted for 400g/L sodium hydroxide solution so that solution temperature is 35~45 DEG C, the PVP solution dissolved is added, is stirred.
(3)Measure 80% hydrazine hydrate(Mass concentration)Solution 50ml, adds 450ml deionized waters and is diluted, in stirring bar The hydrazine hydrate solution diluted was added in 3 minutes under part above-mentioned(2)Solution in reduced, charging finish after, after Continuous stirring 30 minutes.
(4)After after slurries clarification, supernatant liquor is drawn, deionized water washing is added, cyclic washing 11 times is to electrical conductivity 12us/cm, vacuum drying is 38h at 80 DEG C, and the ultrafine palladium powder specific surface area of preparation is 45.43m2/ g, average grain diameter is 2.5um。
Embodiment 2
(1)By 50g High Purity Palladiums with 480mL aqua regia dissolutions into chlorine palladium acid solution, adding deionized water makes cumulative volume be 2000ml, dense Spend for 2.4%(Calculated with simple substance palladium).
(2)The aqueous solution that 0.2gPVP is dissolved into 0.2% with deionized water is weighed, it is stand-by.(1)Middle addition 250ml concentration It is PH=10~11, water-bath for 400g/L Carbon Dioxide sodium solution adjusting body system so that solution temperature is 35~45 DEG C, then is added Enter the PVP solution dissolved, stir.
(3)Measure 80% hydrazine hydrate(Mass concentration)Solution 50ml, adds 450ml deionized waters and is diluted, in stirring bar The hydrazine hydrate solution diluted was added in 3 minutes under part above-mentioned(2)Solution in reduced, charging finish after, after Continuous stirring 30 minutes.
(4)After after slurries clarification, supernatant liquor is drawn, deionized water washing is added, cyclic washing 15 times to electrical conductivity is 18s/cm, vacuum drying is 38h at 80 DEG C, and the ultrafine palladium powder specific surface area of preparation is 75.8 m2/ g, average grain diameter is 4.6um.
Embodiment 3
(1)By 25g High Purity Palladiums with 250mL aqua regia dissolutions into chlorine palladium acid solution, adding deionized water makes cumulative volume be 1000ml, dense Spend for 2.4%(Calculated with simple substance palladium)
(2)The aqueous solution that 0.05gPVP is dissolved into 0.2% with deionized water is weighed, it is stand-by.(1)Middle addition 500ml concentration is 400g/L sodium hydroxide solution adjustment system is PH=10~11, water-bath so that solution temperature is 30~40 DEG C.
(3)Weigh 50g and analyze pure glucose, plus 500ml deionized waters are dissolved, will dissolve under agitation Glucose solution was added to above-mentioned in 3 minutes(2)Solution in reduced, charging finish after, continue stir 30 minutes.Treat After slurries clarification, supernatant liquor is drawn, deionized water washing is added, cyclic washing 15 times to electrical conductivity is 18s/cm, and vacuum is dried Do as 38h at 80 DEG C, the ultrafine palladium powder specific surface area of preparation is 25.3 m2/ g, average grain diameter is 4.2um.
The foregoing is only a preferred embodiment of the present invention, is not intended to limit the scope of the present invention.

Claims (10)

1. the preparation method of high-specific surface area ultrafine palladium powder, it is characterised in that comprise the following steps:
(1)High Purity Palladium aqua regia dissolution is into chlorine palladium acid solution, and obtained solution is the first solution;
(2)Weigh polyvinylpyrrolidone and aqueous povidone solution is dissolved into deionized water, it is stand-by;In the first solution It is PH=9~12 to plant and add aqueous slkali adjustment system, then adds the aqueous povidone solution dissolved and stirs, Obtained solution is the second solution, and controls the temperature of the second solution;
(3)By reducing agent deionized water dissolved dilution, obtained solution is the 3rd solution, and the 3rd solution is slowly added into second Solution is reduced, after addition is finished, and is continued to stir 30 minutes, is obtained ultrafine palladium powder slurries;
(4)After after the clarification of ultrafine palladium powder slurries, supernatant liquor is drawn, deionized water washing, cyclic washing to electrical conductivity ﹤ is added 20us/cm, and vacuum drying, that is, the product obtained are ultrafine palladium powder.
2. the preparation method of high-specific surface area ultrafine palladium powder according to claim 1, it is characterised in that:The step(1) In be into chlorine palladium acid solution, to add High Purity Palladium aqua regia dissolution deionized water adjustment solution concentration, solution is calculated with simple substance palladium Concentration is 2.0%~4.0%.
3. the preparation method of high-specific surface area ultrafine palladium powder according to claim 1, it is characterised in that:The step(2) The consumption of middle polyvinylpyrrolidone is the 0.1%~0.5% of the mass parts of High Purity Palladium.
4. the preparation method of high-specific surface area ultrafine palladium powder according to claim 1, it is characterised in that:The step(2) In aqueous slkali be natrium carbonicum calcinatum or sodium hydroxide.
5. the preparation method of high-specific surface area ultrafine palladium powder according to claim 1, it is characterised in that:The step(2) The middle temperature for controlling the second solution is 30~50 DEG C.
6. the preparation method of high-specific surface area ultrafine palladium powder according to claim 1, it is characterised in that:The step(3) The reducing agent of middle selection is hydrazine hydrate, glucose.
7. the preparation method of high-specific surface area ultrafine palladium powder according to claim 1, it is characterised in that:The step(3) The middle adition process time that 3rd solution is slowly added to the second solution is 1~3min.
8. the preparation method of high-specific surface area ultrafine palladium powder according to claim 1, it is characterised in that:The step(4) Middle mode of washing washs for mashing.
9. the preparation method of high-specific surface area ultrafine palladium powder according to claim 1, it is characterised in that:The step(4) Middle vacuum drying is that 36~42h is dried under 80 DEG C of vacuum condition.
10. the ultra-fine palladium of high-specific surface area made from the preparation method of high-specific surface area ultrafine palladium powder according to claim 1 Powder.
CN201710450372.8A 2017-06-15 2017-06-15 High-specific surface area ultrafine palladium powder and preparation method thereof Pending CN107052362A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109865845A (en) * 2019-03-29 2019-06-11 无锡英特派金属制品有限公司 The preparation method of high-density palladium powder
CN115070058A (en) * 2022-08-16 2022-09-20 西安锐创微米科技有限公司 Preparation method of high-crystallinity and high-sphericity palladium powder with strong oxidation resistance
CN115889799A (en) * 2022-10-28 2023-04-04 广东微容电子科技有限公司 Preparation method of spherical nano palladium powder for high-end MLCC inner electrode slurry

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04333503A (en) * 1991-05-09 1992-11-20 Sumitomo Metal Mining Co Ltd Production of fine palladium powder
JPH06299211A (en) * 1993-04-14 1994-10-25 Mitsubishi Materials Corp Production of oxidation resistant palladium powder
JPH0784607B2 (en) * 1988-03-03 1995-09-13 田中貴金属工業株式会社 Method for producing fine palladium particles
JPH10330810A (en) * 1997-06-05 1998-12-15 Tanaka Kikinzoku Kogyo Kk Manufacture of palladium particle
CN101279375A (en) * 2008-01-16 2008-10-08 南京大学 Preparation of Pd nano particle
CN102172776A (en) * 2011-01-25 2011-09-07 西安凯立化工有限公司 Method for preparing metal palladium powder
US20130202909A1 (en) * 2012-02-06 2013-08-08 Lg Chem, Ltd. Method of producing metal nanoparticles
CN104028774A (en) * 2014-06-11 2014-09-10 励福实业(江门)贵金属有限公司 Activated palladium powder and preparation method and application thereof
CN106270545A (en) * 2015-06-12 2017-01-04 中国振华集团云科电子有限公司 A kind of high-tap density noble metal raw powder's production technology
CN106573302A (en) * 2014-08-19 2017-04-19 贺利氏德国有限两合公司 Method for preparing active palladium(0) powder

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0784607B2 (en) * 1988-03-03 1995-09-13 田中貴金属工業株式会社 Method for producing fine palladium particles
JPH04333503A (en) * 1991-05-09 1992-11-20 Sumitomo Metal Mining Co Ltd Production of fine palladium powder
JPH06299211A (en) * 1993-04-14 1994-10-25 Mitsubishi Materials Corp Production of oxidation resistant palladium powder
JPH10330810A (en) * 1997-06-05 1998-12-15 Tanaka Kikinzoku Kogyo Kk Manufacture of palladium particle
CN101279375A (en) * 2008-01-16 2008-10-08 南京大学 Preparation of Pd nano particle
CN102172776A (en) * 2011-01-25 2011-09-07 西安凯立化工有限公司 Method for preparing metal palladium powder
US20130202909A1 (en) * 2012-02-06 2013-08-08 Lg Chem, Ltd. Method of producing metal nanoparticles
CN104028774A (en) * 2014-06-11 2014-09-10 励福实业(江门)贵金属有限公司 Activated palladium powder and preparation method and application thereof
CN106573302A (en) * 2014-08-19 2017-04-19 贺利氏德国有限两合公司 Method for preparing active palladium(0) powder
CN106270545A (en) * 2015-06-12 2017-01-04 中国振华集团云科电子有限公司 A kind of high-tap density noble metal raw powder's production technology

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
郑杰等: "优质超细钯粉的研制", 《粉末冶金技术》 *
马喜宏 张文栋: "液相法制备纳米钯粉的工艺研究", 《中北大学学报自然科学版》 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109865845A (en) * 2019-03-29 2019-06-11 无锡英特派金属制品有限公司 The preparation method of high-density palladium powder
CN115070058A (en) * 2022-08-16 2022-09-20 西安锐创微米科技有限公司 Preparation method of high-crystallinity and high-sphericity palladium powder with strong oxidation resistance
CN115070058B (en) * 2022-08-16 2022-11-01 西安锐创微米科技有限公司 Preparation method of high-crystallinity and high-sphericity palladium powder with strong oxidation resistance
CN115889799A (en) * 2022-10-28 2023-04-04 广东微容电子科技有限公司 Preparation method of spherical nano palladium powder for high-end MLCC inner electrode slurry
CN115889799B (en) * 2022-10-28 2023-10-20 广东微容电子科技有限公司 Preparation method of spherical nano palladium powder for high-end MLCC inner electrode slurry

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