CN1872917A - In situ method for preparing modified Nano powder of hydrate, hydroxy salt, and oxide - Google Patents
In situ method for preparing modified Nano powder of hydrate, hydroxy salt, and oxide Download PDFInfo
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- CN1872917A CN1872917A CN 200510017642 CN200510017642A CN1872917A CN 1872917 A CN1872917 A CN 1872917A CN 200510017642 CN200510017642 CN 200510017642 CN 200510017642 A CN200510017642 A CN 200510017642A CN 1872917 A CN1872917 A CN 1872917A
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- organic modifier
- propyl carbinol
- oxide
- stearic acid
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Abstract
This invention discloses an in situ method for preparing modified hydroxide, hydroxyl salt and oxide nanopowders. The method comprises: (1) utilizing organic medium n-butanol or benzene and water on the surface of the primary nanoparticles to form an azeotrope, and distilling the azeotrope; (2) utilizing the heat produced by distillation to bond the organic modifier and the hydroxyls on the surface of the nanoparticles to achieve in situ modification of the nanopowders. The distilled n-butanol or benzene can be recovered, thus producing little pollution. The obtained nanopowders can be distilled in weak polar or nonpolar solvent, thus can solve the problem of dispersion of nanoscale additives in plastics, rubbers, fibers and lubricating oils.
Description
Technical field
The invention belongs to the nano material preparation technical field, particularly a kind of organic modifier that adds in the azeotropic distillation drying nano-powder makes organic modifier generate the method for the nanoparticle of surface modification at the nanoparticle surface reaction in.
Background technology
Nanoparticle is owing to have special roles such as surface effects, quantum size effect, small-size effect, joins material property is largely increased, thereby becomes the focus of current material circle research.But the surfactivity that nanoparticle is bigger can cause their agglomerations in use again, so nanoparticle is carried out surface modification, solves its scattering problem in material, becomes the bottleneck problem that nano material is applied.The nanoparticle that the precipitator method or sol-gel method prepare, the surface exists a large amount of hydroxyls and water molecules, when carrying out drying with traditional method, usually because the bridge linking effect of interparticle capillary phenomenon and water molecules hydrogen bond, the phenomenon of growing up can take place to assemble between the nanoparticle, nanoparticle in the original liquid of result, usually become bigger coacervate after the drying even generated hard agglomeration, therefore, cold method, azeotropic drying method, spray-drying process become the common method of current drying nanoparticle.In the azeotropic drying method, propyl carbinol or benzene can form azeotropic system with water, and especially in the azeotropic system of propyl carbinol and water, water-content can be up to 44.5%.When azeotropic, propyl carbinol can replace the water molecules of nanoparticle surface like this, and then moisture content is steamed, and obtains the exsiccant nano-powder.If but powder is applied in the organic system, because the polar difference, also must further carry out organically-modifiedly as required to dried nano-powder, make work become numerous and diverse, and can not guarantee that properties-correcting agent to the nanoparticle surface in-situ modification, has a greatly reduced quality modification effect.
Summary of the invention
The object of the invention is to provide the method for a kind of component distillation in-situ preparing modification oxyhydroxide, hydroxyl salt, nm-class oxide powder, and the nano powder physical efficiency of preparation realizes the dispersion of nanometer scale in low-pole and non-polar solvent.
For reaching above-mentioned purpose, the present invention adopts following technical scheme: the method for in-situ preparing modification oxyhydroxide, hydroxyl salt, nm-class oxide powder, nanometer scale primary particle and the organic modifier received at metal hydroxides, hydroxyl metal-salt or the metal oxide of water or the preparation of water alcohol mixed system are dispersed in organic reaction medium propyl carbinol or the benzene, and component distillation carries out the surface in situ reaction.
Organic modifier is lipid acid RCOOH, soap RCOOM or coupling agent, and R is C
8-C
18The straight or branched alkyl, M is Na, K, Mg, Ca, Al or Zn.
Coupling agent is silane, titanic acid ester, aluminic acid ester or zirconate; Metal in oxyhydroxide, hydroxyl salt, the oxide compound is transition metal, IIA, IIIA, IVA or VA metallic element.
Temperature of reaction is 50-200 ℃, and the reaction times is 0.5-24 hour, and the concentration of organic modifier in reaction medium is 1-1000mmol/L, and the mol ratio of organic modifier and nano-powder is 1: 10-100.
Reaction medium is a propyl carbinol, and the mol ratio of organic modifier and propyl carbinol is 1: 5-300.
Characteristics of the present invention are to add organic modifier in azeotropic system, in the azeotropic drying nanoparticle, chemical bonding takes place in coating materials and nano-particle surface functional group, the hard aggregation phenomenon that capillary phenomenon when not only greatly degree has reduced owing to the nanoparticle drying forms, and successfully realized coating in the nanoparticle surface original position.Modifier not only can produce sterically hindered effect and prevent that further particle from growing up like this, and can change the character of nanoparticle surface, becomes lipophilicity by original wetting ability.The scattering problem of fine thus solution nanoparticle in materials such as plastics, rubber, polymeric fibrous material neutral lubrication oil (ester) oil product reaches the purpose of surface modification.Propyl carbinol that component distillation goes out or benzene can reclaim and reuse easily, can not cause environmental pollution.Very big change can not take place in the nanoparticle after the modification not only pattern, and good dispersion effect is arranged in nonpolar medium.This is different from the method for original wet processing nanoparticle, traditional wet processing is to dried nano-powder, again be distributed in the dispersion medium, add modifier then and carry out modification, this method is difficult to the assurance modifier primary particle of nanometer scale is modified, because dried nanoparticle is because capillarity much becomes offspring, or the active group that dry rear surface exists is less or active lower, modifier much is the modification of the coacervate that forms of modification or offspring to offspring to their modification, so modification effect is extremely undesirable, can not realize that nanometer scale disperses at nonpolar medium, not reach nanoparticle and add ideal effect in the material to.
Description of drawings
The nanometer Mg (OH) that Fig. 1 modifies for stearic acid
2The infrared spectrogram of particulate;
The nanometer Mg (OH) that Fig. 2 modifies for stearic acid
2The XRD figure of particulate;
The nanometer Mg (OH) that Fig. 3 modifies for stearic acid
2The TEM figure of particulate;
The nanometer ZnS n (OH) that Fig. 4 modifies for stearic acid
6The infrared spectrogram of particulate;
The nanometer ZnS n (OH) that Fig. 5 modifies for stearic acid
6The TEM figure of particulate.
Embodiment
Example 1, with the MgCl of 10ml 5mol/L
2Solution slowly is added drop-wise in the NaOH solution of 100ml1mol/L, fully stirs, and carries out precipitin reaction in the time of 40 ℃, after reaction finishes, filters, and washing leaching cake is used 0.1mol/LAgNO up to filtrate
3Solution can not detect till the chlorion.Then filter cake is directly joined in the propyl carbinol of 10ml, after ultra-sonic dispersion was even, the stearic acid that adds 0.5g again continued ultrasonic dissolution, after becoming homogeneous system, begin to carry out component distillation, till liquid all steams in system, obtain the stearic nanometer Mg of finishing (OH)
2Particulate.
Stearic acid decorated nanometer Mg (OH)
2The performance perameter of particulate is as follows:
Stearic acid surface-modified nanometer Mg (OH)
2The infrared spectrogram of particulate such as Fig. 1 (test of AVATAR360FT-IR infrared spectrometer), a is the nanometer Mg (OH) for preparing by liquid phase method among the figure
2Particulate in propyl carbinol, obtain after the azeotropic drying infrared absorption curve, b adds the dried infrared absorption curve of stearic acid in azeotropic system, c is b extracting infrared absorption curve after 24 hours in toluene, d is stearic infrared absorption curve.From figure, relatively find out, add the stearic acid drying in the azeotropic system after, stearic acid can be well and Mg (OH)
2Generation coating effect, after the toluene extracting, stearic acid is still to Mg (OH)
2Produce fine coating effect, illustrate that this effect should be a chemical b `.With the stearic acid collection of illustrative plates more as can be seen, the peculiar 1700cm of stearic acid
-1Absorption peak disappears, and further specifies stearic acid and Mg (OH)
2Between produced chemical b `.
X-ray diffractogram such as Fig. 2 (X ' Pert Pro x-ray powder diffraction instrument test) characterize the crystalline structure of sample, and among the figure, a, b are respectively nanometer Mg (OH)
2Particulate and stearic acid decorated nanometer Mg (OH)
2The X-ray diffractogram of particulate, stearic acid is modified Mg (OH) as can be seen
2Do not change Mg (OH)
2Composition, with Mg (OH)
2Diffraction peak matches, and the result shows that two samples meet JCPDS 82-2453 simultaneously, have the hexagonal structure structure.
Transmission electron microscope (test of JEM-2010 projection electron microscope) photo such as Fig. 3, a is the nanometer Mg (OH) that directly carries out azeotropic drying
2The shape appearance figure of microparticulate in ethanol, the pattern of sample is the flap about diameter 100nm as can be seen, and soft-agglomerated phenomenon is to a certain degree arranged.B is the nanometer Mg (OH) after stearic acid modified
2The shape appearance figure of microparticulate in the chloroform, as can be seen, since the certain space steric effect of stearic acid, originally soft-agglomerated nanometer Mg (OH)
2Particulate presents single dispersion phenomenon after stearic acid modified substantially, is the sheet pattern still, and size does not all change, and modified powder is floating fully in water, and the variation explanation stearic acid of dispersing property can be well to nanometer Mg (OH)
2Particulate carries out surface modification.
Example 2, to the La of 100ml 2mol/L (NO
3)
3The Macrogol 4000 magnetic agitation that adds 0.5g in the solution is clear solution, and in induction stirring, the ammonia soln of Dropwise 5 ml25-28% generates gelationus La (OH)
3Precipitation.Being reflected at 80 ℃ carries out finishing after 2 hours, place then and spend the night, filter washing precipitation, then filter cake is directly joined in the propyl carbinol of 10ml, after ultra-sonic dispersion was even, the oleic acid that adds 0.5ml again continued ultra-sonic dispersion, after becoming homogeneous system, the beginning component distillation, refluxed 30 minutes earlier, again liquid in the system is all distillated, obtain finishing oleic acid nanometer La (OH)
3Particulate.
In example 3, ammonia soln dropping 80ml water, 50ml acetone and the 20ml alcoholic acid mixing solutions with 10ml 25-28%, it is transparent to be stirred to solution.BaCl with 10ml 1mol/L
2Solution slowly is added drop-wise to above-mentioned mixed solution under violent stirring, reaction is 8 hours in the time of 75 ℃, after the end, filters, and washing leaching cake is used 0.1mol/L AgNO up to filtrate
3Solution can not detect till the chlorion, then filter cake is directly joined in the propyl carbinol of 10ml, after ultra-sonic dispersion is even, the capric acid that adds 0.5ml again continues ultrasonic dissolution, after becoming homogeneous system, the beginning component distillation, liquid all steams in system, obtains the nanometer Ba (OH) of finishing capric acid
2Particulate.
Example 4, with 0.2mol NaOH and 0.06mol NaCO
3Be dissolved in the 50ml deionized water, in addition with 0.06mol MgCl
26H
2O and 0.02mol AlCl
39H
2O is dissolved in the 100ml deionized water, at 80 ℃, under the agitation condition, above-mentioned alkali lye is added drop-wise to according to certain speed in the mixing solutions of magnalium salt, after 4h is carried out in reaction, filters, and washing leaching cake is used 0.1mol/LAgNO up to filtrate
3Solution can not detect till the chlorion, then filter cake is directly joined in the propyl carbinol of 30ml, after ultra-sonic dispersion is even, the laurostearic acid that adds 0.5g again continues ultrasonic dissolution, after becoming homogeneous system, the beginning component distillation, refluxed 30 minutes earlier, till again liquid in the system all being distillated, obtain the two oxyhydroxide nanoparticles of stratiform Mg-Al type of finishing laurostearic acid.
Example 5, under magnetic agitation, with the ZnSO of 70ml 0.5mol/l
4The aqueous solution dropwise joins the Na of 50ml0.5mol/l
2SnO
3In the aqueous solution, control reaction temperature is 40 ℃, reaction 0.5h, and ageing 1h, with sedimentation and filtration, washing is up to the BaCl of filtrate with 0.1mol/l
2Solution detects less than SO
4 2-Till.Then, wet cake is directly joined in the propyl carbinol of 50ml, ultra-sonic dispersion evenly after, add the stearic acid of 0.5g again, continue ultra-sonic dispersion evenly after, till decompression component distillation liquid in the system all steams, obtain the nanometer ZnS n (OH) that stearic acid is modified
6Particulate.
Stearic acid decorated nanometer ZnS n (OH)
6The performance perameter of particulate is as follows:
The nanometer ZnS n (OH) that stearic acid is modified
6The infrared spectrogram of particulate such as Fig. 4 (test of AVATAR360FT-IR infrared spectrometer), a is the nanometer ZnS n (OH) for preparing by liquid phase method among the figure
6Particulate in propyl carbinol, obtain after the azeotropic drying infrared absorption curve, b adds the dried infrared absorption curve of stearic acid in azeotropic system, relatively find out from a, b, in the b curve at 2920cm
-1And 2850cm
-1There is absorption peak at the place, and this is respectively-CH
3With-CH
2Asymmetric and symmetric vibration absorb, illustrate in the azeotropic system that after the adding stearic acid drying, stearic acid can be well to ZnSn (OH)
6Generation coating effect, the same with embodiment 1, this effect should be a chemical b `, relatively finds out the peculiar 1700cm of stearic acid with the stearic acid infrared absorption curve
-1Absorption peak disappears, and further specifies stearic acid and ZnSn (OH)
6Between produced chemical b `.
Transmission electron microscope (test of JEM-2010 transmission electron microscope) photo such as Fig. 5, a is the nanometer ZnS n (OH) that directly carries out azeotropic drying
6The shape appearance figure of microparticulate in ethanol, sample topography is bead or the square about 100nm as can be seen, and is more inhomogeneous, varies, soft-agglomerated phenomenon is comparatively serious.B is the nanometer ZnS n (OH) after stearic acid modified
6The shape appearance figure of microparticulate in the chloroform, as can be seen, because stearic certain space steric effect, originally more serious soft-agglomerated particle becomes comparatively loose, substantially present single dispersion phenomenon, sample still is the bead or the square of size about 100nm, and modified powder is floating fully in water, and the variation explanation stearic acid of dispersion medium is well to nanometer ZnS n (OH)
6Particulate has carried out modification.
Example 6, the ammonia soln of 10ml 25-28% is added drop-wise in 50ml water and the 50ml alcoholic acid mixing solutions, it is transparent to be stirred to solution.Control reaction temperature is 60 ℃, progressively drips the Pb (Ac) of 1mol/L under magnetic agitation
2Aqueous solution 10ml, carry out precipitin reaction, behind the isothermal reaction 3h, with sedimentation and filtration, washing, then filter cake is directly joined in the propyl carbinol of 10ml, after ultra-sonic dispersion was even, the Zinic stearas that adds 0.5g again continued ultra-sonic dispersion, after becoming homogeneous system, the beginning component distillation till liquid all steams in system, obtains the nanometer PbO particulate of finishing Zinic stearas.
Claims (5)
1, the method for in-situ preparing modification oxyhydroxide, hydroxyl salt, nm-class oxide powder, it is characterized in that, nanometer scale primary particle and organic modifier at metal hydroxides, hydroxyl metal-salt or the metal oxide of the preparation of water or water alcohol mixed system are dispersed in organic reaction medium propyl carbinol or the benzene, and component distillation carries out the surface in situ reaction.
2, the method for claim 1 is characterized in that, organic modifier is lipid acid RCOOH, soap RCOOM or coupling agent, and R is C
8-C
18The straight or branched alkyl, M is Na, K, Mg, Ca, Al or Zn.
3, method as claimed in claim 2 is characterized in that, coupling agent is silane, titanic acid ester, aluminic acid ester or zirconate; Metal in oxyhydroxide, hydroxyl salt, the oxide compound is transition metal, IIA, IIIA, IVA or VA metallic element.
4, as claim 1,2 or 3 described methods, it is characterized in that temperature of reaction is 50-200 ℃, the reaction times is 0.5-24 hour, the concentration of organic modifier in reaction medium is 1-1000mmol/L, and the mol ratio of organic modifier and nano-powder is 1: 10-100.
5, method as claimed in claim 4 is characterized in that, reaction medium is a propyl carbinol, and the mol ratio of organic modifier and propyl carbinol is 1: 5-300.
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| CN106929834A (en) * | 2015-12-31 | 2017-07-07 | 比亚迪股份有限公司 | The surface selective metallization method of inorganic powder surface processing method and chemical plating activator and polymer product and polymer product |
| CN111566052A (en) * | 2018-03-22 | 2020-08-21 | 三菱综合材料株式会社 | Metal oxide fine particles and method for producing same, dispersion for forming infrared shielding film and method for producing same, method for forming infrared shielding film, and substrate with infrared shielding film |
| US11365129B2 (en) | 2017-02-06 | 2022-06-21 | Mitsubishi Materials Corporation | Method for producing metal oxide particles, method for producing dispersion of metal oxide particles, and method for producing infrared shielding film |
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| GB9815270D0 (en) * | 1998-07-14 | 1998-09-09 | Cambridge Display Tech Ltd | Particles and devices comprising particles |
| CN1105741C (en) * | 1998-11-10 | 2003-04-16 | 中国科学院化工冶金研究所 | Microballs of super-paramagnetic polymer and preparing process thereof |
| CN1096487C (en) * | 1999-07-12 | 2002-12-18 | 武汉工业大学 | nm-class composite polyphenylamine-Fe2O3 material and its preparing process |
| DE10064637A1 (en) * | 2000-12-22 | 2002-07-04 | Henkel Kgaa | Nanoparticulate surface-modified titanium oxide and its use in dentifrices |
| DE10163256A1 (en) * | 2001-12-21 | 2003-07-10 | Henkel Kgaa | Surface modified zinc oxide for the production of nanoparticulate dispersions |
| JP4230741B2 (en) * | 2002-08-30 | 2009-02-25 | 日立ソフトウエアエンジニアリング株式会社 | Purification method of semiconductor nanoparticles |
| CN1493608A (en) * | 2003-09-02 | 2004-05-05 | 华东理工大学 | Nano-ferroferric oxide/polystyrene magnetic composite material and its preparation method |
| CN1256282C (en) * | 2004-05-27 | 2006-05-17 | 上海交通大学 | Preparing method for polymer grafting and modifying titanium dioxide nanometer tube |
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| CN102105245A (en) * | 2008-07-23 | 2011-06-22 | 建筑研究和技术有限公司 | Method for producing metal nanoparticles in polyols |
| CN106929834A (en) * | 2015-12-31 | 2017-07-07 | 比亚迪股份有限公司 | The surface selective metallization method of inorganic powder surface processing method and chemical plating activator and polymer product and polymer product |
| US11365129B2 (en) | 2017-02-06 | 2022-06-21 | Mitsubishi Materials Corporation | Method for producing metal oxide particles, method for producing dispersion of metal oxide particles, and method for producing infrared shielding film |
| US11535523B2 (en) | 2018-02-14 | 2022-12-27 | Mitsubishi Materials Corporation | Method for producing metal oxide dispersion liquid and method for producing infrared-radiation-shielding film |
| CN111566052A (en) * | 2018-03-22 | 2020-08-21 | 三菱综合材料株式会社 | Metal oxide fine particles and method for producing same, dispersion for forming infrared shielding film and method for producing same, method for forming infrared shielding film, and substrate with infrared shielding film |
| CN111566052B (en) * | 2018-03-22 | 2023-06-23 | 三菱综合材料株式会社 | Dispersion for forming metal oxide fine particles and infrared shielding film, process for producing the same, process for producing the film, and substrate having the film |
| US11796725B2 (en) | 2018-03-22 | 2023-10-24 | Mitsubishi Materials Corporation | Metal oxide microparticles, method for producing same, dispersion for forming infrared-shielding film, method for producing same, method for forming infrared-shielding film, and base material having infrared-shielding film |
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