+

US20070039417A1 - Method for preparing nano-complex-powder comprising multiple components and silver - Google Patents

Method for preparing nano-complex-powder comprising multiple components and silver Download PDF

Info

Publication number
US20070039417A1
US20070039417A1 US11/206,052 US20605205A US2007039417A1 US 20070039417 A1 US20070039417 A1 US 20070039417A1 US 20605205 A US20605205 A US 20605205A US 2007039417 A1 US2007039417 A1 US 2007039417A1
Authority
US
United States
Prior art keywords
silver
solution
nano
complex
powder
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.)
Abandoned
Application number
US11/206,052
Inventor
Dehuan Huang
Zongquan Li
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to US11/206,052 priority Critical patent/US20070039417A1/en
Assigned to HUANG, DEHUAN reassignment HUANG, DEHUAN ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LI, ZONGQUAN, HUANG, DEHUAN
Publication of US20070039417A1 publication Critical patent/US20070039417A1/en
Abandoned legal-status Critical Current

Links

Images

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
    • 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
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy

Definitions

  • the present invention relates to a complex material comprising silver, and more particularly to a nano-complex-powder comprising multiple components and silver.
  • Metal silver is effective against microorganisms.
  • the effect for anti-bacteria or sterilization is highly enhanced when the silver particle size is in nano-scale.
  • Nano-silver attracts high attention from scientific and industrial fields both domestically and abroad because of its characteristics of broad and high effect, environmental protection, and causing no side effect.
  • Metals, other than silver, such as zinc and copper, are also effective against microorganisms.
  • Applications of nano-complex-silver-zinc-copper powder are more effective and broadly due to the coordination in the multiply antibacterial components. Additionally, nano-complex-powder comprising multiply components and silver also has a high application value in some special conductive materials.
  • the primary object of the present invention is to provide a method for preparing a nano-complex-powder comprising multiply components and silver.
  • the method comprises the steps of:
  • the advantages of the present invention is that a nano-complex-powder comprising multiple components and silver is achievable, wherein the particle size is 10-100 nm, and the complex elements and contents are adjustable according to practical requirements; raw materials are obtained easily, the process is simple, low cost, and easily industrialized; the application of the nano-complex-powder comprising multiple components and silver is wide and can be used as a nano-antibacteria and special conductive materials.
  • Application of nano-complex-silver-zinc-copper powder is more effective and broadly due to the coordination in the multiple antibacterial components.
  • FIG. 1 shows a TEM (transmission electron microscope) micrograph of the silver particle according to Example 1 of the present invention.
  • FIG. 2 shows a TEM micrograph of the silver particle according to Example 2 of the present invention.
  • FIG. 3 shows a TEM micrograph of the silver particle according to Example 3 of the present invention.
  • a composition of the nano-complex-powder comprising multiple components and silver is selected from the group consisting of 80.0-99.8% Ag: 0.1-20.0% Zn: 0.001% Fe: 0.001% Cu; 80.0-99.8% Ag: 0.001% Zn: 0.1%-20.0% Fe: 0.001% Cu; 60.0-99.7% Ag: 0.1-20.0% Zn: 0.1-20.0% Fe: 0.001% Cu; 60.0-99.7% Ag: 0.1-20.0% Zn: 0.001% Fe: 0.1-20.0% Cu; 60.0-99.7% Ag: 0.001% Zn: 0.1%-20% Fe: 0.1-20.0% Cu; and 40.0-99.6% Ag: 0.1-20.0% Zn: 0.1-20.0% Fe: 0.1-20.0% Cu.
  • the surfactant may be sodium lauryl sulfate, sodium dodecyl sulphate, polyvinylpyrrolidone, or sodium polyphosphate.
  • One or more than one of the aforementioned surfactants can be used in the present invention.
  • the molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, polyvinylpyrrolidone, sodium lauryl sulfate, and hydrazine hydrate is 1.0: 0.18: 0.0007: 0.0009: 0.0085: 0.12:0.68.
  • Addition of hydrazine hydrate solution is stopped when pH value reaches 6.5-7.5. The solution is stirred for another 10-30 minutes continuously to obtain a solution comprising multiple nano-complex-particle.
  • the reaction product above is stayed for 12 hours to allow the nano-silver particles inert.
  • the nano-complex-powder comprising multiple components and silver is obtained after separation, washing and dry at low temperature. There are 90.1% of silver, 9.8% of zinc, and little amount of iron in the product powder, the average particle size in the powder being 20 nm.
  • the molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, polyvinylpyrrolidone, sodium lauryl sulfate, and hydrazine hydrate is 1.0: 0.21: 0.0007: 0.21: 0.235: 0.031:0.92. Addition of hydrazine hydrate solution is stopped when pH value reaches 7.0. The solution is stirred for another 15 minutes continuously to obtain a solution comprising multiple nano-complex-particle.
  • the reaction product above is stayed for 12 hours to allow the nano-silver particles inert.
  • the nano-complex-powder comprising multiple components and silver is obtained after separation, washing and dry at low temperature. There are 79.8% of silver, 10.1% of zinc, 0.2% of iron and 9.9% of copper in the product powder, and the average particle size in the powder is 18 nm.
  • the molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, polyvinylpyrrolidone, sodium lauryl sulfate and hydrazine hydrate is 1.0: 0.28: 0.15: 0.0038: 0.0089: 0.25:1.13.
  • Addition of hydrazine hydrate solution is stopped when pH value reaches 7.0.
  • the solution is stirred for another 15 minutes continuously to obtain a solution comprising multiple nano-complex-particle.
  • the reaction product above is stayed for 12 hours to allow the nano-silver particles inert.
  • the nano-complex-powder comprising multiple components and silver is obtained after separation, washing and dry at low temperature. There are 80.2% of silver, 13.6% of zinc, 6.1% of iron and 0.1% of copper in the product powder, and the average particle size in the powder is 26 nm.
  • the molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, polyvinylpyrrolidone, sodium lauryl sulfate and hydrazine hydrate is 1.0: 0.81: 0.95: 0.82: 0.027: 0.96:3.71.
  • Addition of hydrazine hydrate solution is stopped when pH value reaches 7.0.
  • the solution is stirred for another 15 minutes continuously to obtain a solution comprising multiple nano-complex-particle.
  • the reaction product above is stayed for 12 hours to allow the nano-silver particles inert.
  • the nano-complex-powder comprising multiple components and silver is obtained after separation, washing and dry at low temperature. There are 40.7% of silver, 19.9% of zinc, 19.9% of iron and 19.5% of copper in the product powder.
  • the molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, polyvinylpyrrolidone, sodium lauryl sulfate and hydrazine hydrate is 1.0: 0.18: 0.0141: 0.18: 0.026: 0.62: 1.01. Addition of hydrazine hydrate solution is stopped when pH value reaches 7.0. The solution is stirred for another 15 minutes continuously to obtain a solution comprising multiple nano-complex-particle.
  • the reaction product above is stayed for 12 hours to allow the nano-silver particles inert.
  • the nano-complex-powder comprising multiple components and silver is obtained after separation, washing and dry at low temperature. There are 77.6% of silver, 8.4% of zinc, 5.7% of iron and 8.3% of copper in the product powder.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacture Of Metal Powder And Suspensions Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Disclosed is a method for preparing nano-complex-powder comprising multiple components and silver. The method includes the steps of mixing 0.01-5.0% (weight percentage concentration) of silver nitrate solution with 0.001-5.0% of zinc nitrate solution, 0.001-5.0% of iron nitrate solution and 0.001-5.0% of copper nitrate solution, adding adequate amount of surfactant solution, and adding 0.001-1.0% of hydrazine hydrate gradually with stirring, and the solution is mixed for another 10-30 minutes to obtain a solution comprising multiple nano-complex-particle. After inertness, washing and drying at low temperature, the nano-complex-powder comprising multiple components and silver is obtained. The silver content in the product powder is about 40-99.6%, and the particle size is 10-100 nm. An advantage of the present invention is that a nano-complex-powder comprising multiple components and silver is achievable, wherein the particle size is 10-100 nm, and the complex elements and contents are adjustable according to practical requirements and the particle is uniform; raw materials are obtained easily, the process is simple, low cost, and easily industrialized. The application of the nano-complex-powder comprising multiple components and silver is wide and can be used as a nano-antibacteria and special conductive materials. Applications of nano-complex-silver-zinc-copper powder is more effective and broadly due to the coordination in the multiple antibacterial components.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The present invention relates to a complex material comprising silver, and more particularly to a nano-complex-powder comprising multiple components and silver.
  • 2. The Prior Arts
  • Metal silver is effective against microorganisms. The effect for anti-bacteria or sterilization is highly enhanced when the silver particle size is in nano-scale. Nano-silver attracts high attention from scientific and industrial fields both domestically and abroad because of its characteristics of broad and high effect, environmental protection, and causing no side effect. Metals, other than silver, such as zinc and copper, are also effective against microorganisms. Applications of nano-complex-silver-zinc-copper powder are more effective and broadly due to the coordination in the multiply antibacterial components. Additionally, nano-complex-powder comprising multiply components and silver also has a high application value in some special conductive materials.
  • SUMMARY OF THE INVENTION
  • The primary object of the present invention is to provide a method for preparing a nano-complex-powder comprising multiply components and silver. The method comprises the steps of:
  • (1) Mixing 0.01-5.0% (weight percentage concentration) of silver nitrate solution with 0.001-5.0% of zinc nitrate solution, 0.001-5.0% of iron nitrate solution, and 0.001-5.0% of copper nitrate solution, adding 0.01-5.0% of surfactant solution, and adding 0.001-1.0% of hydrazine hydrate gradually with stirring, a molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, surfactant, and hydrazine hydrate is 1.0:0.001-0.31:0.001-0.48:0.001-0.43:0.001-1.0:0.5-4.5, the addition of hydrazine hydrate solution is stopped when pH value reaches 6.5-7.5, and the solution is mixed for another 10-30 minutes to obtain a solution comprising multiple nano-complex-particles;
  • (2) Staying the reaction product above for 6-12 hours to allow the nano-silver particles inert, obtaining the nano-complex-powder comprising multiple components and silver after separation, washing and drying at low temperature. The silver content in the product is about 40-99.6%, and the particle size is 10-100 nm.
  • The advantages of the present invention is that a nano-complex-powder comprising multiple components and silver is achievable, wherein the particle size is 10-100 nm, and the complex elements and contents are adjustable according to practical requirements; raw materials are obtained easily, the process is simple, low cost, and easily industrialized; the application of the nano-complex-powder comprising multiple components and silver is wide and can be used as a nano-antibacteria and special conductive materials. Application of nano-complex-silver-zinc-copper powder is more effective and broadly due to the coordination in the multiple antibacterial components.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 shows a TEM (transmission electron microscope) micrograph of the silver particle according to Example 1 of the present invention.
  • FIG. 2 shows a TEM micrograph of the silver particle according to Example 2 of the present invention.
  • FIG. 3 shows a TEM micrograph of the silver particle according to Example 3 of the present invention.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
  • A composition of the nano-complex-powder comprising multiple components and silver is selected from the group consisting of 80.0-99.8% Ag: 0.1-20.0% Zn: 0.001% Fe: 0.001% Cu; 80.0-99.8% Ag: 0.001% Zn: 0.1%-20.0% Fe: 0.001% Cu; 60.0-99.7% Ag: 0.1-20.0% Zn: 0.1-20.0% Fe: 0.001% Cu; 60.0-99.7% Ag: 0.1-20.0% Zn: 0.001% Fe: 0.1-20.0% Cu; 60.0-99.7% Ag: 0.001% Zn: 0.1%-20% Fe: 0.1-20.0% Cu; and 40.0-99.6% Ag: 0.1-20.0% Zn: 0.1-20.0% Fe: 0.1-20.0% Cu.
  • The surfactant may be sodium lauryl sulfate, sodium dodecyl sulphate, polyvinylpyrrolidone, or sodium polyphosphate. One or more than one of the aforementioned surfactants can be used in the present invention.
  • EXAMPLE 1
  • (1) Mix 50 ml of 0.2% (weight percentage concentration) silver nitrate solution with 10 ml of 0.01% zinc nitrate solution, 10 ml of 0.001% iron nitrate solution and 10 ml of 0.001% copper nitrate solution. Next, add 50 ml of 0.1% polyvinylpyrrolidone and 20 ml of 0.1% sodium lauryl sulfate solution into the mixed solution. And, add deionized water to make the solution volume up to 200 ml. Add 200 ml of 0.01% hydrazine hydrate solution into the solution gradually with stirring. The molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, polyvinylpyrrolidone, sodium lauryl sulfate, and hydrazine hydrate is 1.0: 0.18: 0.0007: 0.0009: 0.0085: 0.12:0.68. Addition of hydrazine hydrate solution is stopped when pH value reaches 6.5-7.5. The solution is stirred for another 10-30 minutes continuously to obtain a solution comprising multiple nano-complex-particle.
  • (2) The reaction product above is stayed for 12 hours to allow the nano-silver particles inert. The nano-complex-powder comprising multiple components and silver is obtained after separation, washing and dry at low temperature. There are 90.1% of silver, 9.8% of zinc, and little amount of iron in the product powder, the average particle size in the powder being 20 nm.
  • EXAMPLE 2
  • (1) Mix 50 ml of 0.2% (weight percentage concentration) silver nitrate solution with 11.5 ml of 0.2% zinc nitrate solution, 10 ml of 0.001% iron nitrate solution, and 11.7 ml of 0.2% copper nitrate solution. Next, add 50 ml of 0.1% sodium polyphosphate and 20 ml of 0.1% sodium dodecyl sulphate solution into the mixed solution. And, add deionized water to make the solution volume up to 200 ml. Add 180 ml of 0.015% hydrazine hydrate solution into the solution gradually with stirring. The molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, polyvinylpyrrolidone, sodium lauryl sulfate, and hydrazine hydrate is 1.0: 0.21: 0.0007: 0.21: 0.235: 0.031:0.92. Addition of hydrazine hydrate solution is stopped when pH value reaches 7.0. The solution is stirred for another 15 minutes continuously to obtain a solution comprising multiple nano-complex-particle.
  • (2) The reaction product above is stayed for 12 hours to allow the nano-silver particles inert. The nano-complex-powder comprising multiple components and silver is obtained after separation, washing and dry at low temperature. There are 79.8% of silver, 10.1% of zinc, 0.2% of iron and 9.9% of copper in the product powder, and the average particle size in the powder is 18 nm.
  • EXAMPLE 3
  • (1) Mix 30 ml of 0.8% (weight percentage concentration) silver nitrate solution with 15 ml of 0.5% zinc nitrate solution, 10 ml of 0.5% iron nitrate solution, and 10 ml of 0.001% copper nitrate solution. Next, add 25 ml of 0.5% polyvinylpyrrolidone and 20 ml of 0.5% sodium lauryl sulfate solution into the mixed solution. And, add deionized water to make the solution volume up to 200 ml. Add 200 ml of 0.04% hydrazine hydrate solution into the solution gradually with stirring. The molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, polyvinylpyrrolidone, sodium lauryl sulfate and hydrazine hydrate is 1.0: 0.28: 0.15: 0.0038: 0.0089: 0.25:1.13. Addition of hydrazine hydrate solution is stopped when pH value reaches 7.0. The solution is stirred for another 15 minutes continuously to obtain a solution comprising multiple nano-complex-particle.
  • (2) The reaction product above is stayed for 12 hours to allow the nano-silver particles inert. The nano-complex-powder comprising multiple components and silver is obtained after separation, washing and dry at low temperature. There are 80.2% of silver, 13.6% of zinc, 6.1% of iron and 0.1% of copper in the product powder, and the average particle size in the powder is 26 nm.
  • EXAMPLE 4
  • (1) Mix 20 ml of 0.5% (weight percentage concentration) silver nitrate solution with 18 ml of 0.5% zinc nitrate solution, 27 ml of 0.5% iron nitrate solution and 18 ml of 0.5% copper nitrate solution. Next, add 20 ml of 0.8% polyvinylpyrrolidone and 20 ml of 0.8% sodium lauryl sulfate solution into the mixed solution. And, add deionized water to make the solution volume up to 200 ml. Add 200 ml of 0.055% hydrazine hydrate solution into the solution gradually with stirring. The molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, polyvinylpyrrolidone, sodium lauryl sulfate and hydrazine hydrate is 1.0: 0.81: 0.95: 0.82: 0.027: 0.96:3.71. Addition of hydrazine hydrate solution is stopped when pH value reaches 7.0. The solution is stirred for another 15 minutes continuously to obtain a solution comprising multiple nano-complex-particle.
  • (2) The reaction product above is stayed for 12 hours to allow the nano-silver particles inert. The nano-complex-powder comprising multiple components and silver is obtained after separation, washing and dry at low temperature. There are 40.7% of silver, 19.9% of zinc, 19.9% of iron and 19.5% of copper in the product powder.
  • EXAMPLE 5
  • (1) Mix 5 ml of 0.2% (weight percentage concentration) silver nitrate solution with 20 ml of 0.1% zinc nitrate solution, 20 ml of 0.1% iron nitrate solution and 20 ml of 0.1% copper nitrate solution. Next, add 30 ml of 0.5% polyvinylpyrrolidone and 20 ml of 0.5% sodium lauryl sulfate solution into the mixed solution. And, add deionized water to make the solution volume up to 200 ml. Add 200 ml of 0.015% hydrazine hydrate solution into the solution gradually with stirring. The molar ratio of silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, polyvinylpyrrolidone, sodium lauryl sulfate and hydrazine hydrate is 1.0: 0.18: 0.0141: 0.18: 0.026: 0.62: 1.01. Addition of hydrazine hydrate solution is stopped when pH value reaches 7.0. The solution is stirred for another 15 minutes continuously to obtain a solution comprising multiple nano-complex-particle.
  • (2) The reaction product above is stayed for 12 hours to allow the nano-silver particles inert. The nano-complex-powder comprising multiple components and silver is obtained after separation, washing and dry at low temperature. There are 77.6% of silver, 8.4% of zinc, 5.7% of iron and 8.3% of copper in the product powder.

Claims (2)

1. A method for preparing nano-complex-powder comprising multiple components and silver, comprising the steps of:
(1) mixing 0.01-5.0% (weight percentage concentration) of silver nitrate solution with 0.001-5.0% of zinc nitrate solution, 0.001-5.0% of iron nitrate solution and 0.001-5.0% of copper nitrate solution, adding 0.01-5.0% of surfactant solution into the mixed solution, and adding 0.001-1.0% of hydrazine hydrate gradually with stirring, molar ratio of the silver nitrate, zinc nitrate, iron nitrate, and copper nitrate, surfactant, and hydrazine hydrate being 1.0: 0.001-0.31: 0.001-0.48: 0.001-0.43: 0.001-1.0: 0.5-4.5, stopping the addition of hydrazine hydrate solution when pH value reaches 6.5-7.5, and mixing the solution for another 10-30 minutes to obtain a solution comprising multiple nano-complex-particle; and
(2) staying the reaction product obtained in step (1) for 6-12 hours to allow nano-silver particles inert, obtaining the nano-complex-powder comprising multiple components and silver after separation, washing and drying at low temperature, wherein the silver content in the product powder is 40-99.6%, and the particle size in the powder is 10-100 nm.
2. The method as claimed in claim 1, wherein composition of the nano-complex-powder comprising multiple components and silver is selected from the group consisting of 80.0-99.8% Ag: 0.1-20.0% Zn: 0.001% Fe: 0.001% Cu, 80.0-99.8% Ag: 0.001% Zn: 0.1%-20.0% Fe: 0.001% Cu, 60.0-99.7% Ag: 0.1-20.0% Zn: 0.1-20.0% Fe: 0.001% Cu, 60.0-99.7% Ag: 0.1-20.0% Zn: 0.001% Fe: 0.1-20.0% Cu, 60.0-99.7% Ag: 0.001% Zn: 0.1%-20% Fe: 0.1-20.0% Cu, and 40.0-99.6% Ag: 0.1-20.0% Zn: 0.1 -20.0% Fe: 0.1-20.0% Cu.
US11/206,052 2005-08-18 2005-08-18 Method for preparing nano-complex-powder comprising multiple components and silver Abandoned US20070039417A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/206,052 US20070039417A1 (en) 2005-08-18 2005-08-18 Method for preparing nano-complex-powder comprising multiple components and silver

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11/206,052 US20070039417A1 (en) 2005-08-18 2005-08-18 Method for preparing nano-complex-powder comprising multiple components and silver

Publications (1)

Publication Number Publication Date
US20070039417A1 true US20070039417A1 (en) 2007-02-22

Family

ID=37766270

Family Applications (1)

Application Number Title Priority Date Filing Date
US11/206,052 Abandoned US20070039417A1 (en) 2005-08-18 2005-08-18 Method for preparing nano-complex-powder comprising multiple components and silver

Country Status (1)

Country Link
US (1) US20070039417A1 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100821664B1 (en) 2008-01-03 2008-04-14 주식회사 태성환경연구소 Manufacturing method of deodorant
US20100090179A1 (en) * 2008-10-14 2010-04-15 Xerox Corporation Carboxylic acid stabilized silver nanoparticles and process for producing same
US20110253949A1 (en) * 2008-12-26 2011-10-20 Dowa Electronics Materials Co., Ltd. Fine silver particle powder, method for manufacturing the same, silver paste using the powder, and method of use of the paste
CN102294492A (en) * 2011-08-04 2011-12-28 翔瑞(泉州)纳米科技有限公司 Polymer surface protection monodisperse nano silver particle and preparation method thereof
CN107486563A (en) * 2017-09-05 2017-12-19 中南大学 A kind of method for improving Nano silver grain antibacterial activity
CN107722643A (en) * 2017-10-25 2018-02-23 宁波科邦华诚技术转移服务有限公司 A kind of preparation method of ionic medical nanometer antibacterial material
CN113331141A (en) * 2021-06-16 2021-09-03 临沂大学 Method for improving tensile mechanical property of silk and silk with high tensile property

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6391087B1 (en) * 1997-06-04 2002-05-21 Mitsui Mining And Smelting Co., Ltd. Copper fine powder and method for preparing the same
US6660058B1 (en) * 2000-08-22 2003-12-09 Nanopros, Inc. Preparation of silver and silver alloyed nanoparticles in surfactant solutions
US20040045916A1 (en) * 1999-08-19 2004-03-11 Klein Richard B. Over-door shoe racks
US20040167257A1 (en) * 2003-01-07 2004-08-26 Hong-Son Ryang Preparation of metal nanoparticles and nanocomposites therefrom
US20060073667A1 (en) * 2004-10-05 2006-04-06 Xerox Corporation Stabilized silver nanoparticles and their use

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6391087B1 (en) * 1997-06-04 2002-05-21 Mitsui Mining And Smelting Co., Ltd. Copper fine powder and method for preparing the same
US20040045916A1 (en) * 1999-08-19 2004-03-11 Klein Richard B. Over-door shoe racks
US6660058B1 (en) * 2000-08-22 2003-12-09 Nanopros, Inc. Preparation of silver and silver alloyed nanoparticles in surfactant solutions
US20040167257A1 (en) * 2003-01-07 2004-08-26 Hong-Son Ryang Preparation of metal nanoparticles and nanocomposites therefrom
US20060073667A1 (en) * 2004-10-05 2006-04-06 Xerox Corporation Stabilized silver nanoparticles and their use

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100821664B1 (en) 2008-01-03 2008-04-14 주식회사 태성환경연구소 Manufacturing method of deodorant
US20100090179A1 (en) * 2008-10-14 2010-04-15 Xerox Corporation Carboxylic acid stabilized silver nanoparticles and process for producing same
US8460584B2 (en) * 2008-10-14 2013-06-11 Xerox Corporation Carboxylic acid stabilized silver nanoparticles and process for producing same
US20110253949A1 (en) * 2008-12-26 2011-10-20 Dowa Electronics Materials Co., Ltd. Fine silver particle powder, method for manufacturing the same, silver paste using the powder, and method of use of the paste
US9034214B2 (en) * 2008-12-26 2015-05-19 Dowa Electronics Materials Co., Ltd. Fine silver particle powder, method for manufacturing the same, silver paste using the powder, and method of use of the paste
US20150243400A1 (en) * 2008-12-26 2015-08-27 Dowa Electronics Materials Co., Ltd. Fine silver particle powder, method for manufacturing the same, silver paste using the powder and method of use of the paste
US9721694B2 (en) * 2008-12-26 2017-08-01 Dowa Electronics Materials Co., Ltd. Fine silver particle powder, method for manufacturing the same, silver paste using the powder and method of use of the paste
CN102294492A (en) * 2011-08-04 2011-12-28 翔瑞(泉州)纳米科技有限公司 Polymer surface protection monodisperse nano silver particle and preparation method thereof
CN107486563A (en) * 2017-09-05 2017-12-19 中南大学 A kind of method for improving Nano silver grain antibacterial activity
CN107722643A (en) * 2017-10-25 2018-02-23 宁波科邦华诚技术转移服务有限公司 A kind of preparation method of ionic medical nanometer antibacterial material
CN113331141A (en) * 2021-06-16 2021-09-03 临沂大学 Method for improving tensile mechanical property of silk and silk with high tensile property

Similar Documents

Publication Publication Date Title
Singh et al. Green synthesis of silver nanoparticles using sun dried tulsi leaves and its catalytic application for 4-Nitrophenol reduction
Raveendran et al. A simple and “green” method for the synthesis of Au, Ag, and Au–Ag alloy nanoparticles
Cheng et al. Preparation and characterization of W–Cu nanopowders by a homogeneous precipitation process
CN100528427C (en) Method for preparing nanometer silver composite sol
CN101912976A (en) Method for preparing silver nanoparticles by reduction of plant extract
CN102133646A (en) Preparation method of dispersed iron nanoparticles
US20070039417A1 (en) Method for preparing nano-complex-powder comprising multiple components and silver
Prabu et al. Synthesis and characterization of nanoscale zero valent iron (NZVI) nanoparticles for environmental remediation
Sharma et al. Fe/La/Zn nanocomposite with graphene oxide for photodegradation of phenylhydrazine
CN103008677A (en) Micron-sized flaky silver particles and manufacturing method thereof
CN103273075A (en) HPAA nano-iron particle dispersing method
Mahadevan et al. Investigation of synthesized nanosized copper by polyol technique with graphite powder
Ali et al. Pioneering photocatalysts: WSe2/ZIF-9 Z-scheme nanocomposites for efficient hexavalent chromium removal
Bui et al. Study of stability and antimicrobial activity of colloidal Ag/SiO2 nanocomposites
CN105540577B (en) Method for preparing graphene and graphene composite material by reducing graphene oxide at room temperature
CN102307689A (en) Method for producing dispersed, crystalline, stable to oxidation copper particles
Mandal et al. Wet chemical method for synthesis of superparamagnetic alloyed Ni Pd and Ni Pt nanomagnets in micelles
CN102644066A (en) Environment-friendly chemical nickel plating brightener and application thereof
CN115026294A (en) Low-apparent-density dry-method copper-clad iron powder preparation method, copper-clad iron powder and application thereof
Liu et al. Effect of surfactants on the chemical preparation of tin-silver-copper nanoparticles
CN100384947C (en) Process for preparing silver-based polynary nano composite powder
CN102659553A (en) Method for preparing organocopper bactericide from waste copper clad aluminum leads
Balela et al. Formation of oxidation-stable copper nanoparticles in water
JP6541764B2 (en) Silver-coated copper powder and conductive paste, and method for producing them
Zhang et al. Synthesis of SiO2@ AgCl and SiO2@ Ag3PO4 nanocomposites via replacing reaction in situ towards enhanced photocatalysis

Legal Events

Date Code Title Description
AS Assignment

Owner name: HUANG, DEHUAN, CALIFORNIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HUANG, DEHUAN;LI, ZONGQUAN;REEL/FRAME:016668/0129;SIGNING DATES FROM 20050310 TO 20050314

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION

点击 这是indexloc提供的php浏览器服务,不要输入任何密码和下载