CN1304299C - Process for preparing vanadium dioxide nano powder - Google Patents
Process for preparing vanadium dioxide nano powder Download PDFInfo
- Publication number
- CN1304299C CN1304299C CNB2005100207900A CN200510020790A CN1304299C CN 1304299 C CN1304299 C CN 1304299C CN B2005100207900 A CNB2005100207900 A CN B2005100207900A CN 200510020790 A CN200510020790 A CN 200510020790A CN 1304299 C CN1304299 C CN 1304299C
- Authority
- CN
- China
- Prior art keywords
- oxalic acid
- presoma
- process furnace
- vanadium dioxide
- dioxide nano
- 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.)
- Expired - Fee Related
Links
Images
Landscapes
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
The present invention relates to a preparation method of vanadium dioxide nanometer powder, which orderly comprises the process steps of the preparation of precursors and the thermal decomposition of the precursors. In the preparation of the precursors, V2O5 and oxalic acid are used as raw materials, wherein the weight ratio of the V2O5 to the oxalic acid is 1:1 to 3. The V2O5 and the oxalic acid with the ratio are placed in a reaction container and are stirred by adding water at the temperature of 40 to 70 DEG C until reduction reactions of the V2O5 and the oxalic acid are finished, and an obtained solution is evaporated to obtain solid vanadyl oxalate precursors. The temperature of the precursors is increased to 350 DEG C to 500 DEG C under the vacuum condition at a speed of 3 to 10 DEG C/min, and a power supply of a heating furnace is shut down after the temperature is kept for 20 to 40 minutes. The vacuum degree in the furnace is kept, the temperature of decomposed products is decreased to the room temperature, and the vanadium dioxide nanometer powder materials are obtained. MoO3 or N5H37W6O24 are added when the precursors are prepared, and Mo or W doped vanadium dioxide nanometer powder materials can be obtained.
Description
Technical field
The invention belongs to the preparation method of vanadium dioxide powder material, particularly a kind of preparation method of vanadium dioxide nano powder.
Background technology
VO
2Be a kind of typical phase transition compound, along with the generation of phase transformation, resistivity, susceptibility, optical index, transmissivity and reflectivity are undergone mutation, and phase transition process is a reversible.These characteristics can make VO
2Be applied to buildings intelligent temperature control glass, photoelectric switch material, thermistor material, can wipe optical memory material, blinding laser weapons safety guard, photochromic material, submillimeter wave radiating modulator or the like field.Therefore, to VO
2And preparation method thereof research have crucial value.
Application number is the preparation method that 95196132.2 Chinese patent application discloses a kind of vanadium dioxide particles, this method adopts industrial ammonium hexavanadate (AHV) or is that ammonium hexavanadate (AHV) ammonium of feedstock production is as presoma with ammonium meta-vanadate (AMV), obtain non-adulterated vanadium dioxide particles by pyrolysis, or carry out pyrolysis after in above-mentioned presoma, mixing and obtain adulterated vanadium dioxide particles above-mentioned presoma.Its pyrolysis is to be at least under 100 ℃/minute at temperature about 400 ℃ and 650 ℃ and temperature rise rate to carry out, and is kept within the specific limits and directed contact to few 1/2 hour with reaction medium by the gas that pyrolysis produces, and is preferably 1 hour.The problem that aforesaid method exists is: 1, contain ammonium in the raw material, the content that therefore must control ammonium is to guarantee to obtain VO accurately
2Structure, this brings difficulty to technology controlling and process; 2, presoma pyrolytic temperature rise rate is at least 100 ℃/minute, thereby the power of process furnace is bigger, has increased the cost of equipment; 3, Zhi Bei vanadium dioxide particles granularity is micron order (size is less than micron).
Application number is the preparation method that 00117321.9 Chinese patent application discloses a kind of vanadium dioxide nano powder, steps of the method are: 1) use H
2C
2O
42H
2O and N
2H
42HCl in hydrochloric acid medium with V
2O
5Reduction preparation VOCl
22) with the VOCl that makes
2Solution and (NH
4)
2CO
3Or NH
4HCO
3Prepared in reaction vanadyl (IV) basic carbonate ammonium presoma, in dehydrated alcohol with the presoma ultrasonication to granularity≤2 μ m; 3) with the presoma that makes at inert atmosphere or contain that thermolysis gets VO in the inert atmosphere
2Powder, 350～700 ℃ of Heating temperatures.By the Cr that in presoma, mixes, Mo, W, obtain the vanadium dioxide nano powder of doping Cr, Mo, W.Aforesaid method not only processing step is complicated, and because raw material has adopted hydrochloric acid and ammoniated material, can produce detrimentally affect to environment and operator's health.
Summary of the invention
The objective of the invention is to overcome the deficiencies in the prior art, provide a kind of preparation not mix and the novel method of mixed vanadium dioxide nano powder material, this kind method has not only been simplified technology, helps environmental protection, and is easy to controlling quality.
Technical scheme of the present invention is as follows;
One, the preparation method of mixed vanadium dioxide nano powder material not
Processing step is followed successively by the preparation of presoma and the thermolysis of presoma.
1, the preparation of presoma
With V
2O
5And oxalic acid (H
2C
2O
42H
2O) be raw material, V
2O
5With the weight ratio of oxalic acid be 1: 1～1: 3; V with described proportioning
2O
5Put into reaction vessel and add water with oxalic acid, V is crossed in water logging
2O
5Get final product (add-on of water does not have strict demand) with oxalic acid, stir normal pressure, 40～70 ℃ then, up to V
2O
5(reduction reaction is finished to obtain no sedimentary blue look liquid and is as the criterion, and is generally 2～3 hours) after reduction reaction is finished, promptly obtains solid oxalic acid vanadyl presoma with obtaining solution evaporate to dryness till finishing with the reduction reaction of oxalic acid, and its chemical formula is VO (C
2O
4)
2H
2O.
2, the thermolysis of presoma
The thermolysis of presoma can be selected any technology in following three kinds of technologies for use.
(1) will put into process furnace after the pulverizing of obtaining oxalic acid vanadyl presoma, begin to vacuumize when under normal pressure, being heated to 250 ℃～300 ℃ with the speed of 3～10 ℃/min, and under vacuum condition, continue to be heated to 350 ℃～500 ℃ with the speed of 3～10 ℃/min, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain vanadium dioxide nano powder.
(2) obtaining oxalic acid vanadyl presoma is pulverized the back in process furnace, be heated to 150 ℃～250 ℃ (rate of heating does not have strict demand, can be 5～15 ℃/min) insulation 20～30 minutes, vacuumize then, speed with 3～10 ℃/min under vacuum condition is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain vanadium dioxide nano powder.
(3) will put into process furnace after the pulverizing of obtaining presoma oxalic acid vanadyl, speed with 3～10 ℃/min under vacuum condition is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain vanadium dioxide nano powder.
Two, mix the preparation method of Mo vanadium dioxide nano powder
Processing step is followed successively by the preparation of presoma and the thermolysis of presoma.
1, the preparation of presoma
With V
2O
5, oxalic acid and MoO
3Be raw material, V
2O
5With MoO
3Prescription by weight percentage ratio count: V
2O
594～99%, MoO
31～6%, V
2O
5With the weight ratio of oxalic acid be 1: 1～1: 3;
At first with the V of described proportioning
2O
5With MoO
3Put into heating container after mixing and under normal pressure, be heated to molten state (temperature is 800 ℃～900 ℃), pour into this melt in the reaction vessel that water is housed then and stir that (add-on of water does not have strict demand, can disperse V
2O
5With MoO
3Melt gets final product), in above-mentioned solution, add oxalic acid and proceed stirring again, (reduction reaction is finished to obtain no sedimentary blue look liquid and is as the criterion till reduction reaction is finished, be generally 2～4 hours), after reduction reaction is finished, obtaining solution evaporate to dryness is promptly obtained being mixed with Mo ionic oxalic acid vanadyl solid precursor.
2, the thermolysis of presoma
The thermolysis of presoma can be selected any technology in following three kinds of technologies for use.
(1) will put into process furnace after the pulverizing of obtaining oxalic acid vanadyl presoma, begin to vacuumize when under normal pressure, being heated to 250 ℃～300 ℃ with the speed of 3～10 ℃/min, and under vacuum condition, continue to be heated to 350 ℃～500 ℃ with the speed of 3～10 ℃/min, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of Mo.
(2) obtaining oxalic acid vanadyl presoma is pulverized the back in process furnace, be heated to 150 ℃～250 ℃ (rate of heating does not have strict demand, can be 5～15 ℃/min) insulation 20～30 minutes, vacuumize then, speed with 3～10 ℃/min under vacuum condition is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of Mo.
(3) will put into process furnace after the pulverizing of obtaining oxalic acid vanadyl presoma, speed with 3～10 ℃/min under vacuum condition is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of Mo.
Three, mix the preparation method of W vanadium dioxide nano powder
Processing step is followed successively by the preparation of presoma and the thermolysis of presoma.
1, the preparation of presoma
With V
2O
5, oxalic acid and N
5H
37W
6O
24Be raw material, V
2O
5With N
5H
37W
6O
24Prescription by weight percentage ratio count: V
2O
594～99%, N
5H
37W
6O
241～6%, V
2O
5With the weight ratio of oxalic acid be 1: 1～1: 3;
V with described proportioning
2O
5, oxalic acid and N
5H
37W
6O
24Put into reaction vessel and add water, V is crossed in water logging
2O
5, oxalic acid and N
5H
37W
6O
24Get final product (add-on of water does not have strict demand), then at normal pressure, 40～70 ℃ are stirred, (reduction reaction is finished to obtain no sedimentary blue look liquid and is as the criterion till reduction reaction is finished, be generally 2～4 hours), after reduction reaction is finished, obtaining solution evaporate to dryness is promptly obtained being mixed with W ionic solid oxalic acid vanadyl presoma;
2, the thermolysis of presoma
The thermolysis of presoma can be selected any technology in the technology in following three for use.
(1) will put into process furnace after the pulverizing of obtaining oxalic acid vanadyl presoma, begin to vacuumize when under normal pressure, being heated to 250 ℃～300 ℃ with the speed of 3～10 ℃/min, and under vacuum condition, continue to be heated to 350 ℃～500 ℃ with the speed of 3～10 ℃/min, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of W;
(2) with after the pulverizing of obtaining oxalic acid vanadyl presoma, in process furnace, be heated to 150 ℃～250 ℃ (rate of heating does not have strict demand, can be 5～15 ℃/min) insulation 20～30 minutes, speed with 3～10 ℃/min is heated to 350 ℃～500 ℃ under vacuum condition again, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of W;
(3) will put into process furnace after the pulverizing of obtaining oxalic acid vanadyl presoma, speed with 3～10 ℃/min under vacuum condition is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of W.
Above-mentioned three kinds of preparation methods, all also adopted following technical measures:
1, raw materials used V
2O
5Be technical grade or chemical reagent-grade.
2, in the presoma preparation process, can add surfactant polyethylene, the add-on of polyoxyethylene glycol is V
2O
52～5% (weight percentage) with the oxalic acid gross weight.
3, in the presoma thermal decomposition steps, the vacuum degree control in the process furnace is at 20Pa～60Pa.
4, thermolysis is obtained doping and mixed vanadium dioxide nano powder material and carry out anneal, the technology of withdrawing from a secret society or underworld gang is to be warmed up to 400 ℃～600 ℃ insulations 1～4 hour under vacuum condition, and (vacuum tightness is 10～20Pa) to be cooled to room temperature under vacuum condition then.
The present invention has following beneficial effect:
1, owing to is V with oxalic acid
2O
5Reductive agent, thereby pollution-free, help environmental protection and operator's health, and be easy to control the quality of vanadium dioxide nano powder.
2, V
2O
5Can directly obtain presoma oxalic acid vanadyl with the reduction reaction of oxalic acid, thereby simplify the technical process of presoma preparation.
3, the different metallic element technology of mixing is simple, easy to operate.
4, the presoma heat decomposition temperature is low, and the resolving time is short, helps save energy.
5, presoma thermolysis rate of heating is slow, thereby the power requirement of process furnace is less, can less facility investment.
6, add tensio-active agent in the presoma preparation process, help the pulverizing of presoma and the dispersiveness of raising nano-powder.
7, the granularity＜50nm of the vanadium dioxide nano powder that is obtained, powder granule are subsphaeroidal, good uniformity, purity height.
8, the vanadium dioxide nano powder that is obtained has tangible phase change characteristics, and the transformation temperature of the back powder that mixes can be reduced to about 30～35 ℃ by unadulterated 68 ℃.
9, raw material sources extensively, obtain easily are convenient to suitability for industrialized production.
Description of drawings
Fig. 1 is transmission electron microscope (TEM) photo of not mixed vanadium dioxide nano powder material of the present invention;
Fig. 2 is X-ray diffraction (XRD) the analytical results figure of not mixed vanadium dioxide nano powder material of the present invention;
Fig. 3 mixes MoO
3The X-ray diffraction of 3% vanadium dioxide nano powder (XRD) analytical results figure;
Fig. 4 mixes MoO
3The transmission electron microscope of 3% vanadium dioxide nano powder (TEM) photo;
Fig. 5 mixes N
5H
37W
6O
24The X-ray diffraction of 3% vanadium dioxide nano powder (XRD) analytical results figure.
Embodiment
Embodiment 1: prepare not mixed vanadium dioxide nano powder material
| It is 1: 2. | Cross V 2O 5With oxalic acid, finished reduction reaction in 2.5 hours at normal pressure, 60 ℃ of stir abouts, obtaining solution is got oxalic acid vanadyl presoma at 90 ℃ of evaporates to dryness. | 200 ℃ are incubated 25 minutes, vacuumize then, be to be heated to 400 ℃ of insulations with the speed of 5 ℃/min under the condition of 45Pa to close the process furnace power supply after 30 minutes in vacuum tightness, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature, obtain VO 2Nano-powder. | |||
| 4 | Chemical reagent-grade V 2O 5With the weight ratio of oxalic acid be 1: 3. | With V 2O 5Put into reaction vessel and add water logging with oxalic acid and cross V 2O 5With oxalic acid, finish reduction reaction in 2 hours at normal pressure, 70 ℃ of stir abouts, add V then 2O 5With the polyoxyethylene glycol of oxalic acid gross weight 5%, obtaining solution is got oxalic acid vanadyl presoma at 90 ℃ of evaporates to dryness. | To put into tubular oven after the presoma pulverizing, be to be heated to 450 ℃ of insulations with the speed of 8 ℃/min under the condition of 35Pa to close the process furnace power supply after 25 minutes in vacuum tightness, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature, obtain VO 2Nano-powder. | Under vacuum tightness 10Pa condition, be warming up to 600 ℃ of insulations 1 hour, close the process furnace power supply, keep vacuum tightness in the stove, be cooled to room temperature. | ≤ 50nm |
The TEM photo of the not mixed vanadium dioxide nano powder material that present embodiment is prepared as shown in Figure 1, XRD analysis result is as shown in Figure 2.Fig. 1 shows, the granularity＜50nm of the vanadium dioxide nano powder that is obtained, powder granule are subsphaeroidal, good uniformity.Fig. 2 shows that the thermolysis obtained product is the vanadium dioxide crystalline structure.
Embodiment 2: the Mo vanadium dioxide nano powder is mixed in preparation
First group: select technical grade V for use
2O
5, V
2O
5With MoO
3Prescription by weight percentage ratio count: V
2O
599%, MoO
31%; V
2O
5With the weight ratio of oxalic acid be 1: 1.
(1) preparation of presoma
V with said ratio
2O
5With MoO
3Put into container after mixing, under normal pressure, be heated to 800 ℃ and become molten states, pour into this melt in the reaction vessel that water is housed then and stir that (add-on of water is can disperse V
2O
5With MoO
3Melt gets final product), in above-mentioned solution, add the oxalic acid that measures and proceed stirring again, till reduction reaction is finished (about 3 hours), after finishing, reduction reaction obtains no sedimentary blue look liquid, obtaining solution is promptly obtained being mixed with Mo ionic oxalic acid vanadyl solid precursor at 90 ℃ of evaporates to dryness.
(2) thermolysis of presoma
To put into tubular oven after the pulverizing of obtaining oxalic acid vanadyl presoma, begin to vacuumize when under normal pressure, being heated to 250 ℃ with the speed of 3 ℃/min, vacuum degree control is at 55Pa, under vacuum condition, continue to be heated to 350 ℃ with the speed of 3 ℃/min, be incubated and close the process furnace power supply after 40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to the vanadium dioxide nano powder that room temperature promptly obtains to mix Mo.This granularity of mixing the Mo vanadium dioxide nano powder is≤40nm that transformation temperature is 60 ℃.
Second group: select chemical reagent-grade V for use
2O
5, V
2O
5With MoO
3Prescription by weight percentage ratio count: V
2O
597%, MoO
33%; V
2O
5With the weight ratio of oxalic acid be 1: 1.5.
(1) preparation of presoma
V with said ratio
2O
5With MoO
3Put into container after mixing, under normal pressure, be heated to 850 ℃ and become molten states, pour into this melt in the reaction vessel that water is housed then and stir that (add-on of water is can disperse V
2O
5With MoO
3Melt gets final product), in above-mentioned solution, add oxalic acid and the V that measures again
2O
5With the polyoxyethylene glycol of oxalic acid gross weight 3% and proceed to stir, till reduction reaction is finished (about 2.5 hours), obtain no sedimentary blue look liquid after reduction reaction is finished, obtaining solution is promptly obtained being mixed with Mo ionic oxalic acid vanadyl solid precursor at 80 ℃ of evaporates to dryness.
(2) thermolysis of presoma
Obtaining oxalic acid vanadyl presoma is pulverized the back in tubular oven, be heated to 150 ℃ of insulations 30 minutes with 8 ℃/min, vacuumize then, speed with 5 ℃/min under vacuum tightness 45Pa condition is heated to 400 ℃, be incubated and close the process furnace power supply after 30 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of Mo.This granularity of mixing the Mo vanadium dioxide nano powder is≤50nm that transformation temperature is 50 ℃.
The XRD analysis result who mixes the Mo vanadium dioxide nano powder that present embodiment is prepared as shown in Figure 3, the TEM photo is as shown in Figure 4.Fig. 3 shows that the thermolysis obtained product is the vanadium dioxide crystalline structure.Fig. 4 shows that the granularity≤50nm that mixes the Mo vanadium dioxide nano powder that is obtained, powder granule are subsphaeroidal, good uniformity.
The 3rd group: select chemical reagent-grade V for use
2O
5, V
2O
5With MoO
3Prescription by weight percentage ratio count: V
2O
595%, MoO
35%; V
2O
5With the weight ratio of oxalic acid be 1: 2.
(1) preparation of presoma
V with said ratio
2O
5With MoO
3Put into container after mixing, under normal pressure, be heated to 900 ℃ and become molten states, pour into this melt in the reaction vessel that water is housed then and stir that (add-on of water is can disperse V
2O
5With MoO
3Melt gets final product), in above-mentioned solution, add oxalic acid and the V that measures again
2O
5With the polyoxyethylene glycol of oxalic acid gross weight 4% and proceed to stir, till reduction reaction is finished (about 2.5 hours), obtain no sedimentary blue look liquid after reduction reaction is finished, obtaining solution is promptly obtained being mixed with Mo ionic oxalic acid vanadyl solid precursor at 100 ℃ of evaporates to dryness.
(2) thermolysis of presoma
To put into tubular oven after the pulverizing of obtaining oxalic acid vanadyl presoma, speed with 7 ℃/min under vacuum tightness 35Pa condition is heated to 450 ℃, be incubated and close the process furnace power supply after 25 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of Mo.
(3) annealing
Under vacuum tightness 20Pa condition, be warming up to 600 ℃ of insulations 1 hour, close the process furnace power supply, keep vacuum tightness in the stove, be cooled to room temperature.
This granularity of mixing the Mo vanadium dioxide nano powder is≤50nm that transformation temperature is 40 ℃.
The 4th group: select technical grade V for use
2O
5, V
2O
5With MoO
3Prescription by weight percentage ratio count: V
2O
594%, MoO
36%; V
2O
5With the weight ratio of oxalic acid be 1: 3.
(1) preparation of presoma
V with said ratio
2O
5With MoO
3Put into heating container after mixing, under normal pressure, be heated to 900 ℃ and become molten states, pour into this melt in the reaction vessel that water is housed then and stir that (add-on of water is can disperse V
2O
5With MoO
3Melt gets final product), in above-mentioned solution, add the oxalic acid that measures and proceed stirring again, till reduction reaction is finished (about 2 hours), obtain no sedimentary blue look liquid after reduction reaction is finished, obtaining solution is promptly obtained being mixed with Mo ionic oxalic acid vanadyl solid precursor at 100 ℃ of evaporates to dryness.
(2) thermolysis of presoma
To put into tubular oven after the pulverizing of obtaining oxalic acid vanadyl presoma, speed with 7 ℃/min under vacuum tightness 25Pa condition is heated to 500 ℃, be incubated and close the process furnace power supply after 20 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of Mo.
(3) annealing
Under vacuum tightness 10Pa condition, be warming up to 500 ℃ of insulations 2 hours, close the process furnace power supply, keep vacuum tightness in the stove, be cooled to room temperature.
This granularity of mixing the Mo vanadium dioxide nano powder is≤50nm that transformation temperature is 35 ℃.
Embodiment 3: the W vanadium dioxide nano powder is mixed in preparation
First group: select technical grade V for use
2O
5, V
2O
5With N
5H
37W
6O
24Prescription by weight percentage ratio count: V
2O
599%, N
5H
37W
6O
241%; V
2O
5With the weight ratio of oxalic acid be 1: 1
(1) preparation of presoma
V with described proportioning
2O
5, oxalic acid, N
5H
37W
6O
24And V
2O
5Putting into reaction vessel with the polyoxyethylene glycol of oxalic acid gross weight 2% adds water and carries out stir about and finished reduction reaction in 3 hours normal pressure, 40 ℃, the add-on of water was flooded with the raw material in the reaction vessel is advisable, after reduction reaction is finished, obtain no sedimentary blue look liquid, obtaining solution is promptly obtained being mixed with W ionic solid oxalic acid vanadyl presoma at 80 ℃ of evaporates to dryness.
(2) thermolysis of presoma
To put into tubular oven after the pulverizing of obtaining oxalic acid vanadyl presoma, begin to vacuumize when under normal pressure, being heated to 250 ℃ with the speed of 3 ℃/min, vacuum degree control is at 55Pa, under vacuum condition, continue to be heated to 350 ℃ with the speed of 3 ℃/min, be incubated and close the process furnace power supply after 40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to the vanadium dioxide nano powder that room temperature promptly obtains to mix W.
This granularity of mixing the W vanadium dioxide nano powder is≤40nm that transformation temperature is 40 ℃.
Second group: select chemical reagent-grade V for use
2O
5, V
2O
5With N
5H
37W
6O
24Prescription by weight percentage ratio count: V
2O
597%, N
5H
37W
6O
243%; V
2O
5With the weight ratio of oxalic acid be 1: 1.5.
(1) preparation of presoma
V with described proportioning
2O
5, oxalic acid, N
5H
37W
6O
24Putting into reaction vessel adds water and carries out stir about and finished reduction reaction in 3 hours normal pressure, 50 ℃, the add-on of water was advisable to flood with the raw material in the reaction vessel, after reduction reaction is finished, obtain no sedimentary blue look liquid, obtaining solution is promptly obtained being mixed with W ionic solid oxalic acid vanadyl presoma at 90 ℃ of evaporates to dryness.
(2) thermolysis of presoma
Obtaining oxalic acid vanadyl presoma is pulverized the back in tubular oven, be heated to 150 ℃ of insulations 30 minutes with 5 ℃/min, vacuumize then, speed with 5 ℃/min under vacuum tightness 45Pa condition is heated to 400 ℃, be incubated and close the process furnace power supply after 30 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of W.
(3) annealing
Under vacuum tightness 20Pa condition, be warming up to 500 ℃ of insulations 2 hours, close the process furnace power supply, keep vacuum tightness in the stove, be cooled to room temperature.
This granularity of mixing the W vanadium dioxide nano powder is≤50nm that transformation temperature is 32 ℃.
The XRD analysis result who mixes the W vanadium dioxide nano powder that present embodiment is prepared as shown in Figure 5, this figure shows that the thermolysis obtained product is the vanadium dioxide crystalline structure.
The 3rd group: select chemical reagent-grade V for use
2O
5, V
2O
5With N
5H
37W
6O
24Prescription by weight percentage ratio count: V
2O
595%, N
5H
37W
6O
245%; V
2O
5With the weight ratio of oxalic acid be 1: 2.
(1) preparation of presoma
V with described proportioning
2O
5, oxalic acid, N
5H
37W
6O
24And V
2O
5Putting into reaction vessel with the polyoxyethylene glycol of oxalic acid gross weight 4% adds water and carries out stir about and finished reduction reaction in 2.5 hours normal pressure, 60 ℃, the add-on of water was advisable to flood with the raw material in the reaction vessel, after reduction reaction is finished, obtain no sedimentary blue look liquid, obtaining solution is promptly obtained being mixed with W ionic solid oxalic acid vanadyl presoma at 100 ℃ of evaporates to dryness.
(2) thermolysis of presoma
To put into tubular oven after the pulverizing of obtaining oxalic acid vanadyl presoma, speed with 7 ℃/min under vacuum tightness 35Pa condition is heated to 450 ℃, be incubated and close the process furnace power supply after 25 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of W.
(3) annealing
Under vacuum tightness 10Pa condition, be warming up to 600 ℃ of insulations 1 hour, close the process furnace power supply, keep vacuum tightness in the stove, be cooled to room temperature.
This granularity of mixing the W vanadium dioxide nano powder is≤50nm that transformation temperature is 30 ℃.
The 4th group: select technical grade V for use
2O
5, V
2O
5With N
5H
37W
6O
24Prescription by weight percentage ratio count: V
2O
594%, N
5H
37W
6O
246%; V
2O
5With the weight ratio of oxalic acid be 1: 3.
(1) preparation of presoma
V with described proportioning
2O
5, oxalic acid, N
5H
37W
6O
24And V
2O
5Putting into reaction vessel with the polyoxyethylene glycol of oxalic acid gross weight 5% adds water and stirs normal pressure, 70 ℃ and finished reduction reaction in 2 hours, the add-on of water was advisable to flood with the raw material in the reaction vessel, after reduction reaction is finished, obtain no sedimentary blue look liquid, obtaining solution is promptly obtained being mixed with W ionic solid oxalic acid vanadyl presoma at 80 ℃ of evaporates to dryness.
(2) thermolysis of presoma
To put into tubular oven after the pulverizing of obtaining oxalic acid vanadyl presoma, speed with 7 ℃/min under vacuum tightness 25Pa condition is heated to 500 ℃, be incubated and close the process furnace power supply after 20 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of W.
This granularity of mixing the W vanadium dioxide nano powder is≤50nm that transformation temperature is 28 ℃.
Claims (6)
1, a kind of preparation method of vanadium dioxide nano powder, processing step is followed successively by the preparation of presoma and the thermolysis of presoma, it is characterized in that:
(1) preparation of presoma
With V
2O
5With oxalic acid be raw material, V
2O
5With the weight ratio of oxalic acid be 1: 1～1: 3, with the V of described proportioning
2O
5Put into reaction vessel and add water with oxalic acid, V is crossed in water logging
2O
5Get final product with oxalic acid, stir normal pressure, 40～70 ℃ then, up to V
2O
5Till finishing with the reduction reaction of oxalic acid, after reduction reaction is finished, obtaining solution evaporate to dryness is promptly obtained solid oxalic acid vanadyl presoma;
(2) thermolysis of presoma
To put into process furnace after the pulverizing of obtaining oxalic acid vanadyl presoma, begin to vacuumize when under normal pressure, being heated to 250 ℃～300 ℃ with the speed of 3～10 ℃/min, vacuum degree control in the process furnace is at 20～60Pa, and under vacuum condition, continue to be heated to 350 ℃～500 ℃ with the speed of 3～10 ℃/min, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain vanadium dioxide nano powder;
Or obtaining oxalic acid vanadyl presoma is pulverized back speed with 5～15 ℃/min in process furnace be heated to 150 ℃～250 ℃ insulations 20～30 minutes, vacuumize then, vacuum degree control in the process furnace is at 20～60Pa, speed with 3～10 ℃/min under vacuum condition is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain vanadium dioxide nano powder;
Or will put into process furnace after the pulverizing of obtaining presoma oxalic acid vanadyl, speed with 3～10 ℃/min under the condition of vacuum tightness 20～60Pa is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain vanadium dioxide nano powder.
2, a kind of preparation method of vanadium dioxide nano powder, processing step is followed successively by the preparation of presoma and the thermolysis of presoma, it is characterized in that:
(1) preparation of presoma
With V
2O
5, oxalic acid and MoO
3Be raw material, V
2O
5With MoO
3Prescription by weight percentage ratio count: V
2O
594～99%, MoO
31～6%, V
2O
5With the weight ratio of oxalic acid be 1: 1～1: 3, at first with the V of described proportioning
2O
5With MoO
3Put into heating container after mixing and under normal pressure, be heated to molten state, pour into this melt in the reaction vessel that water is housed then and stir, add oxalic acid and proceed stirring in above-mentioned solution again, till reduction reaction was finished, the add-on of water was can disperse V
2O
5With MoO
3Melt gets final product, and after reduction reaction is finished, obtaining solution evaporate to dryness is promptly obtained being mixed with Mo ionic oxalic acid vanadyl solid precursor;
(2) thermolysis of presoma
To put into process furnace after the pulverizing of obtaining oxalic acid vanadyl presoma, begin to vacuumize when under normal pressure, being heated to 250 ℃～300 ℃ with the speed of 3～10 ℃/min, vacuum degree control in the process furnace is at 20～60Pa, and under vacuum condition, continue to be heated to 350 ℃～500 ℃ with the speed of 3～10 ℃/min, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of Mo;
Or obtaining oxalic acid vanadyl presoma is pulverized back speed with 5～15 ℃/min in process furnace be heated to 150 ℃～250 ℃ insulations 20～30 minutes, vacuumize then, vacuum degree control in the process furnace is at 20～60Pa, speed with 3～10 ℃/min under vacuum condition is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of Mo;
Or will put into process furnace after the pulverizing of obtaining oxalic acid vanadyl presoma, speed with 3～10 ℃/min under the condition of vacuum tightness 20～60Pa is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 15～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of Mo.
3, a kind of preparation method of vanadium dioxide nano powder, processing step is followed successively by the preparation of presoma and the thermolysis of presoma, it is characterized in that:
(1) preparation of presoma
With V
2O
5, oxalic acid and N
5H
37W
6O
24Be raw material, V
2O
5With N
5H
37W
6O
24Prescription by weight percentage ratio count: V
2O
594～99%, N
5H
37W
6O
241～6%, V
2O
5With the weight ratio of oxalic acid be 1: 1～1: 3, with the V of described proportioning
2O
5, oxalic acid and N
5H
37W
6O
24Put into reaction vessel and add water, V is crossed in water logging
2O
5, oxalic acid and N
5H
37W
6O
24Get final product, stir normal pressure, 40～70 ℃ then, till reduction reaction is finished, after reduction reaction is finished, obtaining solution evaporate to dryness is promptly obtained being mixed with W ionic solid oxalic acid vanadyl presoma;
(2) thermolysis of presoma
To put into process furnace after the pulverizing of obtaining oxalic acid vanadyl presoma, begin to vacuumize when under normal pressure, being heated to 250 ℃～300 ℃ with the speed of 3～10 ℃/min, vacuum degree control in the process furnace is at 20～60Pa, and under vacuum condition, continue to be heated to 350 ℃～500 ℃ with the speed of 3～10 ℃/min, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of W;
Or obtaining oxalic acid vanadyl presoma is pulverized back speed with 5～15 ℃/min in process furnace be heated to 150 ℃～250 ℃ insulations 20～30 minutes, vacuumize then, vacuum degree control in the process furnace is at 20～60Pa, speed with 3～10 ℃/min under vacuum condition is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of W;
Or will put into process furnace after the pulverizing of obtaining oxalic acid vanadyl presoma, speed with 3～10 ℃/min under the condition of vacuum tightness 20～60Pa is heated to 350 ℃～500 ℃, be incubated and close the process furnace power supply after 20～40 minutes, keep the vacuum tightness in the stove, allow degradation production be cooled to room temperature and obtain to mix the vanadium dioxide nano powder of W.
4, according to the preparation method of claim 1 or 2 or 3 described vanadium dioxide nano powders, it is characterized in that with the technology that thermolysis obtains the vanadium dioxide nano powder anneal it being under vacuum condition, to be warmed up to 400 ℃～600 ℃ insulations 1～4 hour, under vacuum condition, be cooled to room temperature then.
5,, it is characterized in that in the presoma preparation process adding that surfactant polyethylene, the add-on of polyoxyethylene glycol are arranged is V according to the preparation method of claim 1 or 2 or 3 described vanadium dioxide nano powders
2O
5With 2～5% of oxalic acid gross weight.
6, according to the preparation method of claim 1 or 2 or 3 described vanadium dioxide nano powders, it is characterized in that V
2O
5Be technical grade or chemical reagent-grade.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100207900A CN1304299C (en) | 2005-04-25 | 2005-04-25 | Process for preparing vanadium dioxide nano powder |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100207900A CN1304299C (en) | 2005-04-25 | 2005-04-25 | Process for preparing vanadium dioxide nano powder |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1693212A CN1693212A (en) | 2005-11-09 |
| CN1304299C true CN1304299C (en) | 2007-03-14 |
Family
ID=35352359
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2005100207900A Expired - Fee Related CN1304299C (en) | 2005-04-25 | 2005-04-25 | Process for preparing vanadium dioxide nano powder |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1304299C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI800666B (en) * | 2018-07-31 | 2023-05-01 | 日商日本化學工業股份有限公司 | Method of producing vanadium dioxide |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100384747C (en) * | 2005-12-16 | 2008-04-30 | 大连理工大学 | Method for preparing high purity vanadium dioxide particles |
| CN100421844C (en) * | 2006-12-11 | 2008-10-01 | 武汉大学 | Preparing process for vanadium dioxide powder |
| CN101786798B (en) * | 2009-12-31 | 2013-03-20 | 中国科学院上海硅酸盐研究所 | Vanadium-based multiple coating liquid, composite film and preparation method and application thereof |
| CN101734720B (en) * | 2009-12-31 | 2013-05-29 | 中国科学院上海硅酸盐研究所 | Method for preparing vanadium dioxide ultrafine powder |
| CN101863511B (en) * | 2010-07-05 | 2013-05-22 | 中国科学技术大学 | Method for preparing monoclinic phase vanadium dioxide and doped nano powder thereof |
| CN102398919B (en) * | 2010-09-08 | 2013-07-17 | 中国科学院上海硅酸盐研究所 | Preparation method of rutile phase vanadium dioxide |
| CN101955751A (en) * | 2010-10-15 | 2011-01-26 | 华东师范大学 | Porous nano plate phase-change material formed by carambola-shaped VO2 and preparation method thereof |
| CN103057333B (en) * | 2012-12-18 | 2015-06-24 | 焦作市金谷轩绞胎瓷艺术有限公司 | Method for manufacturing twistable glaze artistic porcelain chrysanthemum ornamentation |
| CN104071843A (en) * | 2013-03-30 | 2014-10-01 | 中国科学院合肥物质科学研究院 | Preparation method of monodispersed M-phase vanadium dioxide nanoparticles |
| CN104974028A (en) * | 2015-06-23 | 2015-10-14 | 攀钢集团攀枝花钢钒有限公司 | Preparation method of solid vanadyl oxalate |
| CN105388191A (en) * | 2015-11-19 | 2016-03-09 | 天津大学 | Preparation method of ceramic-based vanadium oxide nano rod structured room temperature CH4 sensor |
| CN105540667A (en) * | 2015-12-30 | 2016-05-04 | 山东海容节能新材料有限公司 | Preparation method of doping modified vanadium dioxide powder with lower phase transition temperature |
| JP6990153B2 (en) * | 2018-07-31 | 2022-02-03 | 日本化学工業株式会社 | Manufacturing method of vanadium dioxide |
| CN110947420B (en) * | 2019-10-28 | 2023-04-25 | 江汉大学 | Preparation method of modified composite nano photocatalyst |
| CN112158883A (en) * | 2020-10-16 | 2021-01-01 | 成都先进金属材料产业技术研究院有限公司 | Process for preparing vanadium dioxide nano powder |
| CN112239229B (en) * | 2020-10-19 | 2022-03-22 | 成都先进金属材料产业技术研究院股份有限公司 | Method and device for preparing spherical VO2 nano powder by ultrasonic atomization method |
| CN112960695B (en) * | 2021-02-19 | 2022-09-06 | 大连民族大学 | Vacuum low-temperature rapid synthesis of M-phase VO 2 Method for producing nanoparticles |
| CN115058145B (en) * | 2022-08-05 | 2023-09-12 | 四川大学 | Vanadium dioxide ink and preparation method thereof, and construction method of terahertz functional device |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55149131A (en) * | 1979-05-09 | 1980-11-20 | Mitsubishi Heavy Ind Ltd | Color reagent for vanadium compound |
| US4374756A (en) * | 1981-09-09 | 1983-02-22 | Koppers Company, Inc. | Vanadium-hydrogen-phosphorus-oxygen catalytic material |
| CN1162949A (en) * | 1994-11-09 | 1997-10-22 | 杰夫科油漆公司 | Vanadium dioxide microparticles, method for preparing same, and use thereof, in particular for surface coating |
| CN1279211A (en) * | 2000-08-04 | 2001-01-10 | 中山大学 | Process for preparing nm-class VO2 powder and nm-class ceramics |
| CN1451633A (en) * | 2002-11-16 | 2003-10-29 | 中山大学 | Method for making vanadium dioxide and its adulterant nanoceramics |
-
2005
- 2005-04-25 CN CNB2005100207900A patent/CN1304299C/en not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55149131A (en) * | 1979-05-09 | 1980-11-20 | Mitsubishi Heavy Ind Ltd | Color reagent for vanadium compound |
| US4374756A (en) * | 1981-09-09 | 1983-02-22 | Koppers Company, Inc. | Vanadium-hydrogen-phosphorus-oxygen catalytic material |
| CN1162949A (en) * | 1994-11-09 | 1997-10-22 | 杰夫科油漆公司 | Vanadium dioxide microparticles, method for preparing same, and use thereof, in particular for surface coating |
| CN1279211A (en) * | 2000-08-04 | 2001-01-10 | 中山大学 | Process for preparing nm-class VO2 powder and nm-class ceramics |
| CN1451633A (en) * | 2002-11-16 | 2003-10-29 | 中山大学 | Method for making vanadium dioxide and its adulterant nanoceramics |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI800666B (en) * | 2018-07-31 | 2023-05-01 | 日商日本化學工業股份有限公司 | Method of producing vanadium dioxide |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1693212A (en) | 2005-11-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1304299C (en) | Process for preparing vanadium dioxide nano powder | |
| CN1693211A (en) | Composite mixed vanadium dioxide nano powder material and its preparation process | |
| CN1088544C (en) | Positive active material for nonaqueous cell and its preparing process | |
| CN1058469C (en) | Vanadium dioxide microparticles, method for preparing same, and use thereof, in particular for surface coating | |
| KR20180095875A (en) | Composite tungsten oxide ultrafine particles and dispersions thereof | |
| CN107983387B (en) | Preparation method and application of carbon nitride/bismuth selenate composite material | |
| CN103754891B (en) | The method of a kind of boron/carbothermic method low-temperature growth hafnium boride powder | |
| CN1274602C (en) | Cobaltosic oxide preparation method for lithium ion battery | |
| Li et al. | Co-precipitation synthesis and two-step sintering of YAG powders for transparent ceramics | |
| JP2011063739A (en) | Microparticle of near infrared ray shielding material, production method therefor, particle dispersion of near infrared ray shielding material, and near infrared ray shielding body | |
| CN105755541A (en) | Method for synthesizing zinc oxide whiskers by using microwave-induced combustion synthesis reaction | |
| CN112007632B (en) | Flower-shaped SnO 2 /g-C 3 N 4 Preparation method of heterojunction photocatalyst | |
| CN101885508A (en) | Method for preparing zinc oxide-doped nano powder controllably on large scale | |
| CN108461725A (en) | Vanadium trioxide hollow microsphere of carbon confinement and its preparation method and application | |
| CN1703372A (en) | Ultrafine particulate titanium oxide with low chlorine and low rutile content, and production process thereof | |
| CN113813944B (en) | Monoatomic rhodium catalyst and preparation method and application thereof | |
| CN1821317A (en) | Process for preparing high infrared radiance energy saving paint | |
| CN100341777C (en) | Method of preparing carbon pellets by using heavy oil residue as raw material | |
| CN1038290A (en) | What can be used as hertzian wave wave absorption body is the composition of the material of base with the barium titanate | |
| CN1362936A (en) | Hexagonal lamellar compound based on indium-zinc oxide | |
| CN1927964A (en) | Infrared resistant coating and preparation process | |
| CN110813277B (en) | Photo-thermal synergistic enhanced full-spectrum response heterostructure photocatalyst and preparation thereof | |
| CN1896321A (en) | Preparation of nano-structured DSA electrolytic electrode | |
| CN1294098C (en) | Titanium silicide coated glass with compound functions prepared by nitrogen protection under normal pressure and preparation method thereof | |
| JP2016163028A (en) | Method of producing thermoelectric material |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20070314 Termination date: 20110425 |