CN101024517A - Method for preparing non-crystal molybdemum sulfide nano powder - Google Patents
Method for preparing non-crystal molybdemum sulfide nano powder Download PDFInfo
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- CN101024517A CN101024517A CN 200710019871 CN200710019871A CN101024517A CN 101024517 A CN101024517 A CN 101024517A CN 200710019871 CN200710019871 CN 200710019871 CN 200710019871 A CN200710019871 A CN 200710019871A CN 101024517 A CN101024517 A CN 101024517A
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Abstract
The invention relates to a manufacture method for amorphous form molybdenum sulphide nanometer powder. The feature is that: it uses solubility molybdenate, thiacetamide, strong acid and dispersing agent as raw material, dissolving solubility molybdenate and thiacetamide into deionized water, adding dispersing agent, adding strong acid in a short time, reacting at constant temperature, absorbing tail gas hydrogen disulfide by NaOH sulotion, filtering, washing, drying the depositing to gain MoSx(=2-4) nanometer powder, using it as precursor, burning and gaining amorphous form molybdenum sulphide nanometer powder that has widely application prospect in lubrication, catalyst and photo-electric-magnetism field.
Description
Technical field
The present invention relates to the preparation method of non-crystal molybdemum sulfide nano powder.
Background technology
The sulfide kind of molybdenum is a lot, and wherein many moly-sulfides belong to amorphous substance, and except minorities such as non-crystalline state molybdenum trisulfide had the fixed stoichiometry, atom was non-whole ratio in many non-crystalline state moly-sulfides.Non-crystalline state moly-sulfide (MoS
x) not only can be used for preparing the crystalline state molybdenumdisulphide with " king of solid lubrication " good reputation, and can directly be used as catalytic material, photoelectric material, lubricant.In addition, in high performance self-lubricating coat in use and photoelectricity coated material, it also shows fine application prospect.Some non-crystalline state moly-sulfides can be by comparatively simple chemical synthesis preparation.For example, the non-crystalline state molybdenum trisulfide can pass through rapid precipitation method and sluggish precipitation, the rapid precipitation method is rapid reaction under acidic conditions with molybdate and sodium sulphite, prepares the non-crystalline state molybdenum trisulfide, but this method is difficult to synthesize non-crystalline state molybdenum trisulfide nano-powder; Sluggish precipitation be by in Sodium orthomolybdate and thioacetamide mixing solutions slowly dripping hydrochloric acid prepare the non-crystalline state molybdenum trisulfide, but still do not report the non-crystalline state molybdenum trisulfide nano-powder that utilizes this method to synthesize to have conformation of rules.Utilize the synthetic non-crystalline state MoS of chemical process with conformation of rules
xNano-powder remains quite difficulty at present, and synthetic method also only limits to hydrothermal method and solvent-thermal method.Hydrothermal method is to utilize molybdate and thioacetamide to be incubated 24 hours down in 180 ℃ in autoclave, prepares the non-crystal molybdemum sulfide nano powder of various forms, in order to obtain well-crystallized's molybdenumdisulphide, also must carry out heating crystallization to product; Solvent-thermal method is in pyridine solvent, under 190 ℃, utilizes the synthetic spherical and piped non-crystalline state moly-sulfide of ammonium molybdate and elemental sulfur, and this method and hydrothermal method are similar, also need carry out in autoclave.When utilizing hydrothermal method and solvent-thermal method to prepare the non-crystalline state moly-sulfide, need special high-tension apparatus, output is few, is difficult to suitability for industrialized production.
Summary of the invention
The present invention is for avoiding above-mentioned existing in prior technology weak point, utilize quick sluggish precipitation to replace traditional sluggish precipitation, a kind of preparation method of easy non-crystal molybdemum sulfide nano powder is provided, comprising hollow ball-shape and particulate state non-crystalline state MoS
xThe preparation of nano-powder, prepared non-crystalline state MoS
xNano-powder can be used as the presoma of preparation crystalline state molybdenum disulfide nano powder, also can directly be used as catalysis, lubricates, field such as photoelectricity.
Non-crystal molybdemum sulfide nano powder preparation method's of the present invention characteristics are to operate as follows:
A, be raw material, be equipped with in following ratio with soluble molybdenum hydrochlorate, thioacetamide, strong acid and dispersion agent:
The mol ratio of soluble molybdenum hydrochlorate and thioacetamide is 1: 1-10;
The solid-to-liquid ratio of soluble molybdenum hydrochlorate and strong acid, dispersion agent is followed successively by 1mol: 1-100L, 1mol: 1-100L;
Wherein, strong acid is that concentration is 3-18molL
-1Hydrochloric acid or sulfuric acid;
B, under 40 ℃ of-99 ℃ of temperature condition, soluble molybdenum hydrochlorate and thioacetamide are dissolved in the deionized water, add dispersion agent again, add strong acid at last, strong acid added in 2 minutes and finishes, and constant temperature reacted 1～300 minute down, and tail gas hydrogen sulfide absorbs with sodium hydroxide solution; Reaction gained throw out after filtration, after the washing, 60-200 ℃ dry 1-24 hour down, obtain hollow ball-shape non-crystalline state MoS
xNano-powder, or particulate state non-crystalline state MoS
xNano-powder, and non-crystalline state MoS
xIn the x value be 2 to 4.
The characteristics of the inventive method also are:
The soluble molybdenum hydrochlorate is Sodium orthomolybdate, potassium molybdate or ammonium molybdate.
Dispersion agent is one or more in polyoxyethylene glycol, OP emulsifying agent, cetyl trimethyl ammonium halide, methyl alcohol, ethanol or the propyl alcohol.
Through the preparation of the inventive method, further application comprises:
With step b gained non-crystalline state MoS
xNano-powder is a presoma, under the protective atmosphere of nitrogen, hydrogen or argon gas, calcines 1～400 minute down in 200 ℃～1000 ℃, obtains the molybdenum disulfide nano powder after the cooling.
Hollow ball-shape non-crystalline state MoS with step b gained
xNano-powder is a presoma, calcines 1～400 minute down in 200 ℃～900 ℃ in protective atmosphere, makes hollow ball-shape molybdenum disulfide nano powder.
Hollow ball-shape non-crystalline state MoS with step b gained
xNano-powder is a presoma, calcines 1～400 minute down in 900 ℃～1000 ℃ in protective atmosphere, makes polyhedral nano molybdenum disulfide powder.
Particulate state non-crystalline state MoS with step b gained
xNano-powder is a presoma, calcines 1～400 minute down in 200 ℃～1000 ℃ in protective atmosphere, obtains particulate state molybdenum disulfide nano powder.
The inventive method can obtain precipitin reaction rapidly and uniformly, thereby obtains hollow ball-shape or particulate state non-crystalline state MoS
xNano-powder.
Compared with the prior art, beneficial effect of the present invention is embodied in:
1, the present invention utilizes quick sluggish precipitation, synthetic non-crystalline state MoS in the aqueous solution
xNano-powder by preparation technology's control, can obtain to comprise hollow ball-shape and granular non-crystalline state moly-sulfide (MoS
x, x=2-4) nano-powder.
2, the present invention is about non-crystalline state moly-sulfide (MoS
x, x=2-4) preparation of nano-powder is lower than 100 ℃ and carries out under the aqueous solution, and the reaction times is short, and easy and simple to handle, synthesis technique is simple, is convenient to amplify produce.
3, the present invention is a presoma with prepared non-crystal molybdemum sulfide nano powder, and calcining can obtain the molybdenum disulfide nano particulate of different shape under protective atmosphere, comprises hollow ball-shape, particulate state, polyhedral nanoparticle.Prepared non-crystalline state MoS
xNano-powder reaches the crystalline state molybdenum disulfide nano powder by its acquisition, has the potential using value in fields such as lubricated, optical material, magneticsubstance, electrode materials, air storage material and catalytic materials.
Description of drawings
Fig. 1 is the inventive method gained non-crystalline state MoS
xThe x-ray diffractogram of powder of nano-powder.
Fig. 2 is the non-crystalline state MoS of the inventive method preparation
xNano-powder after calcining, the x-ray diffractogram of powder of the crystalline state molybdenum disulfide nano powder of acquisition.
Fig. 3 (a), Fig. 3 (b) and Fig. 3 (c) are the non-crystalline state MoS with the inventive method preparation
xThe transmission electron microscope picture of nano-powder.
Fig. 4 (a), Fig. 4 (b), Fig. 4 (c) and Fig. 4 (d) are the non-crystalline state MoS with the present invention's preparation
xNano-powder, the transmission electron microscope picture of the molybdenum disulfide nano powder that obtains behind the calcined crystallization.
Below pass through embodiment, and in conjunction with the accompanying drawings the present invention is further described.
Embodiment:
Embodiment 1:
Under 90 ℃, 4mmol Sodium orthomolybdate and 24mmol thioacetamide are dissolved in the 80mL distilled water, add 5mL polyoxyethylene glycol, 5mL propyl alcohol and 10mL ethanol again, in 2 minutes, add the 15mL 12molL that finishes at last
-1Hydrochloric acid, tail gas hydrogen sulfide absorbs with sodium hydroxide solution.82 ℃ of following isothermal reactions after 5 minutes, with throw out filter, washing and 120 ℃ dry 10 hours down, hollow ball-shape non-crystalline state MoS
xNano-powder.
Then, with hollow ball-shape non-crystalline state MoS
xThe nano-powder porcelain of packing into burns in the boat, puts electric tube furnace into, under nitrogen atmosphere and 780 ℃ of calcinings down, react 50 minutes postcooling, and the taking-up sample obtains hollow ball-shape molybdenum disulfide nano powder.
Embodiment 2:
Under 85 ℃, 4mmol potassium molybdate and 32mmol thioacetamide are dissolved in the 100mL distilled water, add 5mLOP emulsifying agent and 5mL methyl alcohol again, in 2 minutes, add the 15mL 6molL that finishes at last
-1Hydrochloric acid, tail gas hydrogen sulfide absorbs with sodium hydroxide solution.85 ℃ of following isothermal reactions after 5 minutes, with throw out filter, washing and 100 ℃ dry 12 hours down, hollow ball-shape non-crystalline state MoS
xNano-powder.
Then, with hollow ball-shape non-crystalline state MoS
xThe nano-powder porcelain of packing into burns in the boat, puts electric tube furnace into, under nitrogen atmosphere and 680 ℃ of 40 minutes postcooling of calcining down, obtains hollow ball-shape molybdenum disulfide nano powder.
Embodiment 3:
Under 78 ℃, 4mmol ammonium molybdate and 12mmol thioacetamide are dissolved in the 180mL distilled water, add 5mL0.05molL again
-1Cetyl trimethylammonium bromide added the 15mL 5molL that finishes at last in 2 minutes
-1Hydrochloric acid, tail gas hydrogen sulfide absorbs with sodium hydroxide solution.95 ℃ of following isothermal reactions after 10 minutes, with throw out filter, washing and 120 ℃ dry 10 hours down, hollow ball-shape non-crystalline state MoS
xNano-powder.
Then, with hollow ball-shape non-crystalline state MoS
xThe nano-powder porcelain of packing into burns in the boat, puts electric tube furnace into, under argon atmospher and 960 ℃ of 120 minutes postcooling of calcining down, obtains polyhedral molybdenum disulfide nano powder.
Embodiment 4:
Under 80 ℃, 4mmol Sodium orthomolybdate and 24mmol thioacetamide are dissolved in the 100mL distilled water, add 10mL ethanol and 10mL propyl alcohol again, in 2 minutes, add the 20mL 3.6molL that finishes at last
-1Sulfuric acid, tail gas hydrogen sulfide absorbs with sodium hydroxide solution., throw out is filtered, washs and descended dry 10 hours after 5 minutes 85 ℃ of following isothermal reactions, obtain particulate state non-crystalline state MoS at 120 ℃
xNano-powder.
Then, with particulate state non-crystalline state MoS
xThe nano-powder porcelain of packing into burns in the boat, puts electric tube furnace into, under nitrogen atmosphere and 780 ℃ of 30 minutes postcooling of calcining down, obtains particulate state molybdenum disulfide nano powder.
Embodiment 5:
Under 90 ℃, 4mmol Sodium orthomolybdate and 16mmol thioacetamide are dissolved in the 200mL distilled water, add 2mL0.05molL again
-1Cetyl trimethylammonium bromide and 5ml ethanol added the 10mL4mol that finishes at last in 2 minutes
L-1Hydrochloric acid and 5mL 3.6molL
-1Sulfuric acid, tail gas hydrogen sulfide absorbs with sodium hydroxide solution., throw out is filtered, washs and descended dry 10 hours at 120 ℃ after 5 minutes 82 ℃ of following isothermal reactions, obtaining existing hollow ball-shape has granular non-crystalline state MoS again
xNano-powder.
Then, with non-crystalline state MoS
xThe nano-powder porcelain of packing into burns in the boat, puts electric tube furnace into, under nitrogen atmosphere and 780 ℃ of above-mentioned presomas of calcining down, react 50 minutes postcooling, the taking-up sample, and obtaining existing hollow ball-shape has granular molybdenum disulfide nano powder again.
Referring to Fig. 1, the non-crystalline state MoS that obtains with the present invention
xThe X-ray diffraction of nano-powder (XRD) peak is the steamed bun shape diffraction peak of disperse, belongs to amorphous substance, and irrelevant with processing condition.X-ray photoelectron power spectrum (XPS) characterization result shows, the non-crystalline state MoS that obtains with the present invention
xElement sulphur changes with processing condition are different with the ratio of molybdenum element amount of substance in the nano-powder, but all between 1: 2～1: 4.Molybdenum disulfide nano powder among the present invention is by the above-mentioned non-crystalline state MoS of calcining under the protective atmosphere of hydrogen, nitrogen or argon gas
xNano powder preparation, there is crystalline state MoS in the XRD diffraction pattern in (as shown in Figure 2)
2Four main diffraction peaks, show that the nano molybdenum disulfide crystalline state that obtains is good.
Transmission electron microscope photo shown in Fig. 3 (a) shows, the hollow ball-shape non-crystalline state MoS of preparation
xThe diameter of nano-powder is about (as embodiment 1,2,3) about 200nm.
Transmission electron microscope photo shown in Fig. 3 (b) shows, the particulate state non-crystalline state MoS of preparation
xThe average particle size of nano-powder is less than 100nm (as embodiment 4).
Transmission electron microscope photo shown in Fig. 3 (c) shows that can obtain existing hollow ball-shape under proper technical conditions has particulate state non-crystalline state MoS again
xNano-powder (as embodiment 5).
Transmission electron microscope photo Fig. 4 (a) and Fig. 4 (b) show, calcining hollow ball-shape non-crystalline state MoS under protective atmosphere
xNano-powder is hollow ball-shape molybdenum disulfide nano particulate (as embodiment 1,2) being lower than 900 ℃ of following products, is polyhedral nano molybdenum disulfide particulate (as embodiment 3) being higher than 900 ℃ of following products.
Transmission electron microscope photo Fig. 4 (c) shows, calcining particle shape non-crystalline state MoS under protective atmosphere
xNano-powder, that obtain all is particulate state molybdenum disulfide nano particulate (as embodiment 4).
Fig. 4 (d) shows that the existing hollow ball-shape of calcining has particulate state non-crystalline state MoS again under protective atmosphere
xNano-powder (as embodiment 5), can obtain existing hollow ball-shape has particulate state molybdenum disulfide nano powder (as embodiment 5) again.
Claims (3)
1, the preparation method of non-crystal molybdemum sulfide nano powder is characterized in that operating as follows:
A, be raw material, be equipped with in following ratio with soluble molybdenum hydrochlorate, thioacetamide, strong acid and dispersion agent:
The mol ratio of soluble molybdenum hydrochlorate and thioacetamide is 1: 1-10;
The solid-to-liquid ratio of soluble molybdenum hydrochlorate and strong acid, dispersion agent is followed successively by 1mol: 1-100L, 1mol: 1-100L;
Wherein, strong acid is that concentration is 3-18molL
-1Hydrochloric acid or sulfuric acid;
B, under 40 ℃ of-99 ℃ of temperature condition, soluble molybdenum hydrochlorate and thioacetamide are dissolved in the deionized water, add dispersion agent again, add strong acid at last, strong acid added in 2 minutes and finishes, and constant temperature reacted 1～300 minute down, and tail gas hydrogen sulfide absorbs with sodium hydroxide solution; Reaction gained throw out after filtration, after the washing, 60-200 ℃ dry 1-24 hour down, obtain hollow ball-shape non-crystalline state MoS
xNano-powder, or particulate state non-crystalline state MoS
xNano-powder, and non-crystalline state MoS
xIn the x value be 2 to 4.
2, preparation method according to claim 1 is characterized in that described soluble molybdenum hydrochlorate is Sodium orthomolybdate, potassium molybdate or ammonium molybdate.
3, preparation method according to claim 1 is characterized in that described dispersion agent is one or more in polyoxyethylene glycol, OP emulsifying agent, cetyl trimethyl ammonium halide, methyl alcohol, ethanol or the propyl alcohol.
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| CN101420023B (en) * | 2008-12-11 | 2010-06-09 | 浙江大学 | Electrochemical lithium ionic insertion/deinsertion electrode and production method thereof |
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| CN101420023B (en) * | 2008-12-11 | 2010-06-09 | 浙江大学 | Electrochemical lithium ionic insertion/deinsertion electrode and production method thereof |
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| CN104091936A (en) * | 2014-07-17 | 2014-10-08 | 浙江大学 | MoS2 nanotile and graphene composite nanomaterial and preparation method thereof |
| CN104192908A (en) * | 2014-08-25 | 2014-12-10 | 华东师范大学 | Nanosphere encapsulated MoS2 micron hollow sphere structure semiconductor material and preparation method thereof |
| CN106986386A (en) * | 2017-05-03 | 2017-07-28 | 合肥学院 | Method for preparing molybdenum disulfide nanoparticles with controllable product form |
| CN106986386B (en) * | 2017-05-03 | 2018-11-30 | 合肥学院 | Method for preparing molybdenum disulfide nanoparticles with controllable product form |
| CN109243837A (en) * | 2018-09-21 | 2019-01-18 | 江苏大学 | A kind of SnO2/C/MoS2Composite material and preparation method |
| CN109850947A (en) * | 2019-03-22 | 2019-06-07 | 合肥学院 | A kind of method that 12 hetropoly acid ammonium prepares molybdenum disulfide particle |
| CN109850947B (en) * | 2019-03-22 | 2021-09-21 | 合肥学院 | Method for preparing molybdenum disulfide particles from ammonium dodecamolybdenum phosphapolyate |
| CN112850791A (en) * | 2019-11-27 | 2021-05-28 | 天津大学 | Amorphous molybdenum disulfide, preparation method and application thereof |
| CN112850791B (en) * | 2019-11-27 | 2022-09-02 | 天津大学 | Amorphous molybdenum disulfide, preparation method and application thereof |
| CN111793249A (en) * | 2020-07-15 | 2020-10-20 | 安徽江淮汽车集团股份有限公司 | Preparation method of antibacterial agent, polymer composite material and preparation method thereof |
| CN115072783A (en) * | 2022-07-05 | 2022-09-20 | 江西省农业科学院土壤肥料与资源环境研究所 | Method for preparing manganese molybdate nano material through phase inversion reaction in hydrothermal process |
| CN115072783B (en) * | 2022-07-05 | 2023-04-11 | 江西省农业科学院土壤肥料与资源环境研究所 | Method for preparing manganese molybdate nano material through phase inversion reaction in hydrothermal process |
| CN115347083A (en) * | 2022-09-19 | 2022-11-15 | 陕西科技大学 | Morphology-controllable molybdenum disulfide nano material and preparation method and application thereof |
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