CN1740405A - Silver nanometer wire synthesizing process - Google Patents
Silver nanometer wire synthesizing process Download PDFInfo
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- CN1740405A CN1740405A CN 200510060864 CN200510060864A CN1740405A CN 1740405 A CN1740405 A CN 1740405A CN 200510060864 CN200510060864 CN 200510060864 CN 200510060864 A CN200510060864 A CN 200510060864A CN 1740405 A CN1740405 A CN 1740405A
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- ethylene glycol
- nano silver
- silver wire
- glycol solution
- synthetic method
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- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 title claims abstract description 73
- 238000000034 method Methods 0.000 title claims abstract description 18
- 229910052709 silver Inorganic materials 0.000 title claims abstract description 10
- 239000004332 silver Substances 0.000 title claims abstract description 10
- 230000002194 synthesizing effect Effects 0.000 title abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 118
- 238000006243 chemical reaction Methods 0.000 claims abstract description 24
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000011261 inert gas Substances 0.000 claims abstract description 4
- 229910001961 silver nitrate Inorganic materials 0.000 claims abstract description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 31
- 238000005119 centrifugation Methods 0.000 claims description 20
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 18
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 18
- 239000000126 substance Substances 0.000 claims description 18
- 238000010189 synthetic method Methods 0.000 claims description 13
- UGWRVHSFESMVND-UHFFFAOYSA-N silver;ethane-1,2-diol;nitrate Chemical compound [Ag+].OCCO.[O-][N+]([O-])=O UGWRVHSFESMVND-UHFFFAOYSA-N 0.000 claims description 12
- 239000007789 gas Substances 0.000 claims description 11
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 11
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 11
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 11
- 229910052786 argon Inorganic materials 0.000 claims description 9
- 239000011521 glass Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 238000010992 reflux Methods 0.000 claims description 9
- 238000001291 vacuum drying Methods 0.000 claims description 9
- 239000012452 mother liquor Substances 0.000 claims description 8
- 230000035484 reaction time Effects 0.000 claims description 7
- -1 silver ions Chemical class 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 239000012535 impurity Substances 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 230000001681 protective effect Effects 0.000 claims description 2
- 238000000746 purification Methods 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- 239000013078 crystal Substances 0.000 abstract description 11
- 239000000463 material Substances 0.000 abstract description 4
- 230000001105 regulatory effect Effects 0.000 abstract description 2
- 229920000642 polymer Polymers 0.000 abstract 1
- 101710134784 Agnoprotein Proteins 0.000 description 14
- 230000005291 magnetic effect Effects 0.000 description 8
- 239000002070 nanowire Substances 0.000 description 8
- 238000009833 condensation Methods 0.000 description 7
- 230000005494 condensation Effects 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- 238000012423 maintenance Methods 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 7
- 239000000376 reactant Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- 239000002042 Silver nanowire Substances 0.000 description 4
- 239000008367 deionised water Substances 0.000 description 4
- 229910021641 deionized water Inorganic materials 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 239000004567 concrete Substances 0.000 description 2
- 238000002003 electron diffraction Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 230000003592 biomimetic effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000010946 fine silver Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 238000001027 hydrothermal synthesis Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000002127 nanobelt Substances 0.000 description 1
- 239000002114 nanocomposite Substances 0.000 description 1
- 239000002121 nanofiber Substances 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 238000001338 self-assembly Methods 0.000 description 1
- 238000007704 wet chemistry method Methods 0.000 description 1
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Abstract
The present invention belongs to the field of nanometer material preparing technology, and provides a two-step silver nanometer wire synthesizing process with high form selectivity and high efficiency. Under the protection of inert gas, very dilute ethylene glycol solution of silver nitrate is first added into ethylene glycol to prepare silver crystal seed; ethylene glycol solution of silver nitrate in relatively high concentration and ethylene glycol polymer solution in the corresponding concentration and volume are then added into the reaction system with crystal seed; and through crystal growth, silver nanometer wire is obtained. By means of regulating reaction condition, the size and form of the silver nanometer wire may be controlled. The present invention has low reaction cost and high silver nanometer wire yield, and the obtained silver nanometer wire has high purity, good structure and high mechanical performance.
Description
Technical field
The present invention relates to the nano material preparation technical field, specifically relate to a kind of synthetic method of nano silver wire.
Background technology
Monodimension nanometer material, such as nano wire, nanofiber, nanometer rod, nano belt or the like, because physicals and chemical properties such as the electricity of its uniqueness that shows, optics, magnetics are applied to aspects such as nano electron device, nano laser, nanochemistry and biosensor, nano-probe, nano composite material widely.Nano silver wire is most important a kind of in the monodimension nanometer material, and the conduction of its brilliance, heat conductivility, chemical stability also make nano silver wire occupy an important seat on the structure nano-device.Had at present much about nano silver wire synthetic bibliographical information, difference according to its principle, can be divided into following a few class substantially: template, polyvalent alcohol method, hydrothermal method, wet chemistry method, biomimetic synthesis, molecule self-assembly revulsion, electrochemical process or the like [concrete visible document: Z.Jiang, Z.Xie, and et al., Chem.Phys.Lett., 374 (2003) 645; E.Braun, Y.Eichen, and et al., Nature, 391 (1998) 775; H.Yan, S.H.Park, and et al., Science, 301 (2003) 1882; J.H.Song, Y.Wu, and et al.J.Am.Chem.Soc., 123 (2001) 10397; Y.Sun, Y.Xia, Science, 298 (2002) 2176; Y.Sun, Y.Yim, andet al.Chem.Mater.14 (2002) 4736; K.K.Caswell, C.M.Bender, and et al., NanoLett., 3 (2003) 667; Z.Wang, J.Liu, and et al., Chem.Eur.J., 11 (2005) 160; Y.Gao, P.Jiang, and et al., J.Phys.Chem.B, 108 (2004) 12877.].Above the whole bag of tricks has its characteristics separately, needs shortcomings such as special plant and instrument, preparation amount are few, cost is high or the preparation method is complicated, technological process is long but exist in varying degrees.Y.Sun, the employing ethylene glycol that people such as Y.Xia propose promptly adopts to add ready-formed platinum crystal seed as the polyvalent alcohol method of solvent, the method for the nano silver wire of synthetic high quality, high yield under the inducing action of polyvinylpyrrolidone (PVP).This is the comparatively easy method of synthesis of silver nano-wire, but they adopt platinum as crystal seed, this just means the heteroatoms of having introduced non-silver in building-up process, thereby conductivity is exerted an influence, cause the uncertainty of quality product, and present this reaction can only lower concentration (＜carry out under 0.1M).Patent CN1522951A and CN1424163A disclose the method for synthetic single crystal nano silver wire separately, but its synthetic concentration is also lower, is unfavorable for scale preparation.If develop a kind of new polyvalent alcohol method, can be under high density, adopt the lower crystal seed of price, such as silver-colored crystal seed, synthesis of silver nano-wire, so just can obtain output fine silver nano wire bigger, that do not contain other foreign metals, be expected to be applied in various fundamental researchs and the applied research.
Summary of the invention
The object of the present invention is to provide the technology of two step synthesis of silver nano-wire under a kind of inertia protection atmosphere.This technology was divided into for two steps: at first be the silver-colored crystal seed of preparation, thereby be that the control crystal growth gets synthesis of silver nano-wire then.
The concrete steps of the synthetic method of nano silver wire are as follows:
Under protection of inert gas and stirring, under condensing reflux, adopt the oil bath heating, temperature is controlled at 140～200 ℃ (the best is 160～180 ℃), with parts by volume be 1 part, concentration range is 10
-5～10
-1It is in the ethylene glycol solution 2 parts, preheating 10～30min that the Silver Nitrate ethylene glycol solution of M joins parts by volume, and the reaction times is that (the best is 15～20min) to 10～60min; With parts by volume be then 5～10 parts, concentration be the Silver Nitrate ethylene glycol solution of 0.1～1.0M and respective concentration, parts by volume is that 5～30 parts of polymkeric substance ethylene glycol solutions join in the reaction system (according to the ratio of the structural unit and the silver ions of polymkeric substance, be controlled at 1～6), the reaction times is that (the best is 2～3h) to 1～10h; Be cooled to normal temperature, promptly get the reaction mother liquor of nano silver wire.
Adopt the method for centrifugation to purify the reaction mother liquor of resulting nano silver wire, at first reaction mother liquor is moved to centrifuge container, the adding volume is 1～5 times a acetone, in the rotating speed centrifugation of 3000～5000rpm, removes upper solution, stays throw out; Adding volume again is the ethanol or the water of 1～5 times of reaction mother liquor, in the rotating speed centrifugation of 3000～5000rpm, removes upper solution, stays throw out, and this process repeats 1～2 time; The throw out of remainder with ethanol or water-dispersion, is transferred in the watch-glass, more than the vacuum-drying 6h, the nano silver wire after obtaining purifying.
The method that adds Silver Nitrate ethylene glycol solution and polymkeric substance ethylene glycol solution is:
(1) the Silver Nitrate ethylene glycol solution adds, and speed control drips the polymkeric substance ethylene glycol solution simultaneously at 900～2000ml/h, and speed control is at 50～80ml/h;
(2) Silver Nitrate ethylene glycol solution and polymkeric substance ethylene glycol solution drip respectively simultaneously, and speed control is at 50～80ml/h;
(3) Silver Nitrate ethylene glycol solution and polymkeric substance ethylene glycol solution mix the back dropping, and speed control is at 60～100ml/h.
Polymkeric substance is polyvinylpyrrolidone or polyoxyethylene.
Inert protective gas is argon gas or nitrogen.
Silver-colored line purity height after the purification, not platiniferous or golden impurity, mean diameter is 50～200nm, length is 5～100 μ m.
The useful effect that the present invention has is:
1, all are reflected in the reactor and finish, and raw material is easy to get, and technology is simple;
2, the reaction allowable temperature has certain fluctuation range, and is simple to operate;
3, protection of inert gas has improved stability, repeatability and the silver-colored line options and the yield of reaction;
4, adopt Silver Nitrate as unique source metal, guarantee not contain other metallic impurity in the product, reduce cost simultaneously;
5, the polymkeric substance that is adopted is PVP or polyoxyethylene (PEO), and raw material is easy to get;
6, the nano silver wire of gained is dispersed good in multiple solvent.
In a word, the present invention can reduce reaction cost, improves the yield of silver-colored line.And the nano silver wire of this synthesis technique gained has advantages such as purity height, structure and better mechanical property.By changing the reaction times, reaction conditionss such as seed concentration can also be regulated the size and the pattern of nano silver wire.
Description of drawings
Fig. 1 is scanning electronic microscope (SEM) picture of the embodiment of the invention 1 synthetic nano silver wire, and scale is 5 μ m among the figure, and nanowire diameter is about 110nm, length 10～100 μ m;
Fig. 2 is the particle powder X-diffracting spectrum of the embodiment of the invention 1 synthetic nano silver wire;
Fig. 3 is the SEM picture of the embodiment of the invention 2 synthetic nano silver wires, and scale is 5 μ m among the figure, and nanowire diameter is about 90nm, length 10～50 μ m;
Fig. 4 is the SEM picture of the embodiment of the invention 3 synthetic nano silver wires, and scale is 1 μ m among the figure, and nanowire diameter is about 70nm, length 10～50 μ m;
Fig. 5 is the SEM picture of the embodiment of the invention 4 synthetic nano silver wires, and scale is 1 μ m among the figure, and nanowire diameter is about 80nm, length 10～50 μ m;
Fig. 6 is the electron diffraction collection of illustrative plates of the embodiment of the invention 4 synthetic nano silver wires, illustrates that this nano silver wire is a kind of twin crystal structure;
Fig. 7 is the SEM picture of the embodiment of the invention 5 synthetic nano silver wires, and scale is 200nm among the figure, and nanowire diameter is about 180nm, length 3～8 μ m;
Fig. 8 is the SEM picture of the embodiment of the invention 6 synthetic nano silver wires, and scale is 200nm among the figure, and nanowire diameter is about 60nm, length 10～100 μ m;
Fig. 9 is the SEM picture of the embodiment of the invention 7 synthetic nano silver wires, and scale is 200nm among the figure, and nanowire diameter is about 200nm, length 5～10 μ m.
Embodiment
The invention will be further described to enumerate several specific embodiments below.
Embodiment 1:
The airtight 50ml three-necked bottle that condensation reflux unit is housed is vacuumized applying argon gas, and place 160 ℃ of oil baths; Add 2ml ethylene glycol, use magnetic stirrer, preheating 10min; With concentration is 2 * 10
-4The AgNO of M
3Ethylene glycol solution 1ml joins in the three-necked bottle, reaction 15min; Be the AgNO of 0.1M then with concentration
3Ethylene glycol solution 5ml joins in the three-necked bottle, and speed control is at 900ml/h, and dripping 10ml concentration simultaneously is the PVP ethanolic soln of 0.15M, and maintenance speed is reacted 6h at 60ml/h; Behind the reactant naturally cooling, pour the 100ml beaker into, add 30ml acetone and mix, pour centrifuge tube centrifugation 30min under 3000rpm into, remove upper solution; Add 40ml ethanol then, ultrasonic 1min impels precipitation to disperse, and upper solution is removed in centrifugation under 3000rpm again; Repeat once; Nano silver wire after disperseing to purify with 5ml ethanol is then transferred to it in watch-glass again, and vacuum-drying 6h promptly obtains nano silver wire.Fig. 1 is scanning electronic microscope (SEM) picture of present embodiment synthetic nano silver wire; Fig. 2 is the particle powder X-diffracting spectrum of present embodiment synthetic nano silver wire.
Embodiment 2:
The airtight 50ml three-necked bottle that condensation reflux unit is housed is vacuumized applying argon gas, and place 160 ℃ of oil baths; Add 2ml ethylene glycol, use magnetic stirrer, preheating 10min; With concentration is 2 * 10
-4The AgNO of M
3Ethylene glycol solution 1ml joins in the three-necked bottle, reaction 30min; Be the AgNO of 0.1M then with concentration
3Ethylene glycol solution 5ml joins in the three-necked bottle, and speed control is at 1500ml/h, and dripping 10ml concentration simultaneously is the PVP ethylene glycol solution of 0.15M, and maintenance speed is reacted 1h at 100ml/h; Behind the reactant naturally cooling, pour the 100ml beaker into, add 30ml acetone and mix, pour centrifuge tube centrifugation 30min under 5000rpm into, remove upper solution; Add 40ml ethanol then, ultrasonic 1min impels precipitation to disperse, and upper solution is removed in centrifugation under 5000rpm again; Repeat once; Nano silver wire after disperseing to purify with 5ml ethanol is then transferred to it in watch-glass again, and vacuum-drying 6h promptly obtains nano silver wire.Fig. 3 is the SEM picture of present embodiment synthetic nano silver wire.
Embodiment 3:
The airtight 50ml three-necked bottle that condensation reflux unit is housed is vacuumized applying argon gas, and place 200 ℃ of oil baths; Add 2ml ethylene glycol, use magnetic stirrer, at 200 ℃ of following preheating 10min; With concentration is 2 * 10
-4The AgNO of M
3Ethylene glycol solution 1ml joins in the three-necked bottle, reacts 30min down at 200 ℃; Oil bath temperature being reduced to 160 ℃ then, is the AgNO of 0.1M again with concentration
3Ethylene glycol solution 5ml joins in the three-necked bottle, and speed control is at 2000ml/h, and dripping 10ml concentration simultaneously is the PVP ethylene glycol solution of 0.15M, and maintenance speed is reacted 2h at 60ml/h; Behind the reactant naturally cooling, pour the 100ml beaker into, add 30ml acetone and mix, pour centrifuge tube centrifugation 30min under 4000rpm into, remove upper solution; Add 40ml ethanol then, ultrasonic 1min impels precipitation to disperse, and upper solution is removed in centrifugation under 4000rpm again; Repeat once; Nano silver wire after disperseing to purify with 5ml ethanol is then transferred to it in watch-glass again, and vacuum-drying 6h promptly obtains nano silver wire.Fig. 4 is the SEM picture of present embodiment synthetic nano silver wire.
Embodiment 4:
The airtight 50ml three-necked bottle that condensation reflux unit is housed is vacuumized applying argon gas, and place 160 ℃ of oil baths; Add 2ml ethylene glycol, use magnetic stirrer, preheating 10min; With concentration is 2 * 10
-4The AgNO of M
3Ethylene glycol solution 1ml joins in the three-necked bottle, reaction 15min; Be the AgNO of 0.1M then with concentration
3Ethylene glycol solution 5ml joins in the three-necked bottle, and speed control is at 1000ml/h, and dripping 10ml concentration simultaneously is the PVP ethylene glycol solution of 0.3M, and maintenance speed is reacted 2h at 100ml/h; Behind the reactant naturally cooling, pour the 100ml beaker into, add 30ml acetone and mix, pour centrifuge tube centrifugation 30min under 3000rpm into, remove upper solution; Add 40ml ethanol then, ultrasonic 1min impels precipitation to disperse, and upper solution is removed in centrifugation under 3000rpm again; Repeat once; Nano silver wire after disperseing to purify with 5ml ethanol is then transferred to it in watch-glass again, and vacuum-drying 6h promptly obtains nano silver wire.Fig. 5 is the SEM picture of present embodiment synthetic nano silver wire; Fig. 6 is the electron diffraction collection of illustrative plates of present embodiment synthetic nano silver wire.
Embodiment 5:
The airtight 50ml three-necked bottle that condensation reflux unit is housed is vacuumized applying argon gas, and place 160 ℃ of oil baths; Add 2ml ethylene glycol, use magnetic stirrer, preheating 30min; With concentration is 2 * 10
-4The AgNO of M
3Ethylene glycol solution 1ml joins in the three-necked bottle, following reaction 20min; Be the AgNO of 0.8M then with concentration
3Ethylene glycol solution 5ml joins in the three-necked bottle, and speed control is at 1000ml/h, and dripping 10ml concentration simultaneously is the PVP ethylene glycol solution of 0.6M, and maintenance speed is reacted 3h at 100ml/h; Behind the reactant naturally cooling, pour the 100ml beaker into, add 30ml acetone and mix, pour centrifuge tube centrifugation 30min under 4000rpm into, remove upper solution; Add the 40ml deionized water then, ultrasonic 1min impels precipitation to disperse, and upper solution is removed in centrifugation under 4000rpm again; Repeat once; Nano silver wire after disperseing to purify with the 5ml deionized water is then transferred to it in watch-glass again, and vacuum-drying 6h promptly obtains nano silver wire.Fig. 7 is the SEM picture of present embodiment synthetic nano silver wire.
Embodiment 6:
The airtight 50ml three-necked bottle that condensation reflux unit is housed is vacuumized applying argon gas, and place 160 ℃ of oil baths; Add 2ml ethylene glycol, use magnetic stirrer, preheating 10min; With concentration is 2 * 10
-4The AgNO of M
3Ethylene glycol solution 1ml joins in the three-necked bottle, reaction 30min; Be the AgNO of 0.1M then with concentration
3Ethylene glycol solution 5ml and concentration are after the PVP ethylene glycol solution 10ml of 0.3M mixes, to be added drop-wise in the three-necked bottle, and maintenance speed is reacted 4h at 70ml/h; Behind the reactant naturally cooling, pour the 100ml beaker into, add 30ml acetone and mix, pour centrifuge tube centrifugation 30min under 4000rpm into, remove upper solution; Add the 40ml deionized water then, ultrasonic 1min impels precipitation to disperse, and upper solution is removed in centrifugation under 4000rpm again; Repeat once; Nano silver wire after disperseing to purify with the 5ml deionized water is then transferred to it in watch-glass again, and vacuum-drying 6h promptly obtains nano silver wire.Fig. 8 is the SEM picture of present embodiment synthetic nano silver wire.
Embodiment 7:
The airtight 50ml three-necked bottle that condensation reflux unit is housed is vacuumized applying argon gas, and place 160 ℃ of oil baths; Add 2ml ethylene glycol, use magnetic stirrer, preheating 10min; With concentration is 2 * 10
-4The AgNO of M
3Ethylene glycol solution 1ml joins in the three-necked bottle, reaction 15min; Be the AgNO of 0.1M then with concentration
3Ethylene glycol solution 5ml joins in the three-necked bottle, and speed control is at 1000ml/h, and dripping 10ml concentration simultaneously is the PEO ethylene glycol solution of 0.3M, and maintenance speed is reacted 2h at 60ml/h; Behind the reactant naturally cooling, pour the 100ml beaker into, add 30ml acetone and mix, pour centrifuge tube centrifugation 30min under 4000rpm into, remove upper solution; Add 40ml ethanol then, ultrasonic 1min impels precipitation to disperse, and upper solution is removed in centrifugation under 4000rpm again; Repeat once; Nano silver wire after disperseing to purify with 5ml ethanol is then transferred to it in watch-glass again, and vacuum-drying 6h promptly obtains nano silver wire.Fig. 9 is the SEM picture of present embodiment synthetic nano silver wire.
Claims (10)
1. the synthetic method of a nano silver wire is characterized in that:
Under protection of inert gas and stirring, under condensing reflux, adopt the oil bath heating, temperature is controlled at 140～200 ℃, with parts by volume be 1 part, concentration range is 10
-5～10
-1It is that reaction times is 10～60min in the ethylene glycol solution 2 parts, preheating 10～30min that the Silver Nitrate ethylene glycol solution of M joins parts by volume; With parts by volume be then 5～10 parts, concentration be the Silver Nitrate ethylene glycol solution of 0.1～0.8M and respective concentration, parts by volume is that 5～30 parts of polymkeric substance ethylene glycol solutions join in the reaction system, the reaction times is 1～10h; Be cooled to normal temperature, promptly get the reaction mother liquor of nano silver wire.
2. the synthetic method of a kind of nano silver wire according to claim 1, it is characterized in that: adopt the method for centrifugation to purify the reaction mother liquor of resulting nano silver wire, at first reaction mother liquor is moved to centrifuge container, the adding volume is 1～5 times a acetone, rotating speed centrifugation at 3000～5000rpm, remove upper solution, stay throw out; Adding volume again is the ethanol or the water of 1～5 times of reaction mother liquor, in the rotating speed centrifugation of 3000～5000rpm, removes upper solution, stays throw out, and this process repeats 1～2 time; The throw out of remainder with ethanol or water-dispersion, is transferred in the watch-glass, more than the vacuum-drying 6h, the nano silver wire after obtaining purifying.
3. the synthetic method of a kind of nano silver wire according to claim 1, it is characterized in that: oil bath temperature the best is 160～180 ℃.
4. the synthetic method of a kind of nano silver wire according to claim 1 is characterized in that: the polymkeric substance of adding and the molar ratio of Silver Nitrate promptly according to the ratio of the structural unit and the silver ions of polymkeric substance, are controlled at 1～6.
5. the synthetic method of a kind of nano silver wire according to claim 1 is characterized in that: the method that adds Silver Nitrate ethylene glycol solution and polymkeric substance ethylene glycol solution is:
(1) the Silver Nitrate ethylene glycol solution adds, and speed control drips the polymkeric substance ethylene glycol solution simultaneously at 900～2000ml/h, and speed control is at 50～80ml/h;
(2) Silver Nitrate ethylene glycol solution and polymkeric substance ethylene glycol solution drip respectively simultaneously, and speed control is at 50～80ml/h;
(3) Silver Nitrate ethylene glycol solution and polymkeric substance ethylene glycol solution mix the back dropping, and speed control is at 60～100ml/h.
6. the synthetic method of a kind of nano silver wire according to claim 1, it is characterized in that: polymkeric substance is polyvinylpyrrolidone or polyoxyethylene.
7. the synthetic method of a kind of nano silver wire according to claim 1, it is characterized in that: reaction times the best of its first step is 15～20min.
8. the synthetic method of a kind of nano silver wire according to claim 1 is characterized in that: the reaction times the best in its second step is 2～3h.
9. the synthetic method of a kind of nano silver wire according to claim 1, it is characterized in that: inert protective gas is argon gas or nitrogen.
10. the synthetic method of a kind of nano silver wire according to claim 1 and 2 is characterized in that: the silver-colored line purity height after the purification, and not platiniferous or golden impurity, mean diameter is 50～200nm, length is 5～100 μ m.
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| CN102161102A (en) * | 2011-02-12 | 2011-08-24 | 明基材料有限公司 | Nano silver wire and manufacturing method thereof |
| CN102328095A (en) * | 2011-10-14 | 2012-01-25 | 济南大学 | Preparation method of metal silver nanowires with adjustable length and diameter |
| CN102744417A (en) * | 2011-06-16 | 2012-10-24 | 浙江科创新材料科技有限公司 | Method for preparing nano-silver wire with high length-diameter ratio |
| CN102804064A (en) * | 2009-06-09 | 2012-11-28 | 富士胶片株式会社 | Conductive composition, transparent conductive film, display element and integrated solar battery |
| CN102936357A (en) * | 2012-10-31 | 2013-02-20 | 北京化工大学 | Antistatic agent made from silver nanowire and functional carbon nano tube (CNT) and preparation method |
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