CN1253117A - Surficial modification process for SiO2 sol particles - Google Patents
Surficial modification process for SiO2 sol particles Download PDFInfo
- Publication number
- CN1253117A CN1253117A CN 98124657 CN98124657A CN1253117A CN 1253117 A CN1253117 A CN 1253117A CN 98124657 CN98124657 CN 98124657 CN 98124657 A CN98124657 A CN 98124657A CN 1253117 A CN1253117 A CN 1253117A
- Authority
- CN
- China
- Prior art keywords
- sio
- surficial
- colloidal sol
- modification process
- peo
- 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.)
- Granted
Links
Landscapes
- Silicon Compounds (AREA)
Abstract
A surficial modification process of SiO2 sol particles features that the sol-gel method is used to modify the surface of SiO2 sol particle by organic large moleculae, directly preparing SiO2 sol with different space configurations, which provides necessary condition for regulating pore channel property and improving surficial property of material. Its advantages are simple process and convenient operation.
Description
The invention belongs to colloidal sol grain modifying method, relate in particular to a kind of SiO
2The colloidal sol surface modification method.
The develop rapidly of modern science and technology has brought many new opportunities to develop for the material field, from performance and requirement, on the nanometer level implementation structure controlled be the research tendency of nanometer synthetic technology in recent years.Utilize organic macromolecule in solution, to have a conformation, by to SiO
2The finishing of colloidal sol nano colloidal particles, and then modulation colloidal sol network structure is the prerequisite of the controlled nano material synthetic technology of implementation structure.Report SiO at present
2Preparation of nanomaterials is a lot, but relates to controlled to powder structure mostly, and about to SiO
2The report of colloidal sol network structure regulation and control is then considerably less.Chinese invention patent 1145331 relates under the modulation of tensio-active agent, and a kind of controllable grain size non-crystal nm SiO is provided
2Technology of preparing; Collosol structure is not studied, 1150124 modification techniques of having reported a kind of colloidal sol surface of Chinese invention patent is characterized in that can preparing the metal-ceramic composite membrane by the modified metal active constituent.As seen aforesaid method only relates to modification and the technology of preparing to powder, does not almost relate to SiO
2The regulation and control of colloidal sol network structure.
But the purpose of this invention is to provide a kind of modulation SiO
2The colloidal sol surface modification method of colloidal sol network structure.
The present invention adopts sol-gel method to modify SiO by organic macromolecule
2The colloidal sol surface directly prepares the SiO with different spaces conformation
2The colloidal sol network structure.
The present invention includes following steps:
1. add tetraethoxy in half of the total consumption of ethanolic soln, the back that stirs forms solution (I);
2. quantitative water, ammoniacal liquor and additive are added in second half of the total consumption of ethanolic soln, mix the back and form solution (II);
3. in whipping process, solution (II) is slowly added in the solution (I), continue to stir 30 minutes, then mixed solution is changed in the airtight molten device of tetrafluoroethylene over to constant temperature ageing, the SiO that promptly obtains having different spaces conformation network structure
2Colloidal sol;
The proportioning (mol ratio) that it is characterized in that colloidal sol is as follows:
Ethanol: water: additive: ammoniacal liquor: tetraethoxy=
(10-100)∶(0.5-10)∶(0.01-0.1)∶(1.0×10
-5)∶1；
20-260 ℃ of aforesaid ageing temperature, digestion time 0.5 day-1 year.
Aforesaid additive can be polyoxyethylene glycol (PEG), fatty alcohol-polyoxyethylene ether (AEO), polyoxyethylene poly-oxygen propylene aether multipolymer (PEO-PPO-PEO).
Compared with the prior art the present invention has following advantage:
Present method technology is simple, and is easy to operate, and raw material is easy to get, and adopts single stage method can prepare the SiO with various space conformations
2Colloidal sol adds the SiO that polyoxyethylene glycol (PEC) obtains
2Colloidal sol has the cyclic network structure, adds the SiO that fatty alcohol-polyoxyethylene ether (AEO) obtains
2Colloidal sol has bar-shaped network structure, adds the SiO that the anti-polyoxyethylene poly-oxygen propylene aether multipolymer (PEO-PPO-PEO) of fat obtains
2Colloidal sol has dendritic network structure.Be next step regulation and control SiO
2Nano material pore properties and improve surface properties and prepared prerequisite.
Embodiment 1
The 20ml tetraethoxy is dissolved in the dehydrated alcohol of 100ml and stirs 15min; With 3.2ml H
2O, 110ml dehydrated alcohol, 0.1ml6MNH
3H
2O and the abundant mixing of 0.1ml PEG200.With above-mentioned two kinds of colloidal sol mixings, 20 ℃ of following ageings 150 days or 60 ℃ of following ageings 20 days, promptly prepare SiO in the encloses container of the tetrafluoroethylene of packing into then with loop network structure
2Colloidal sol.
Embodiment 2
In the foregoing description 1, also can add 5mlPEG200 or PEG600, under the same conditions, prepare SiO with loop network structure
2Colloidal sol.
Embodiment 3
In the foregoing description 1, also can add 10mlPEG200 or PEG600, under the same conditions, prepare SiO with loop network structure
2Colloidal sol.
Embodiment 4
In the foregoing description 1, also can add the 0.1ml polymerization degree and be 3 the AEO or the polymerization degree and be 15 AEO, under the same conditions, prepare SiO with bar-shaped network structure
2Colloidal sol.
Embodiment 5
In the foregoing description 1, also can add the 5ml polymerization degree and be 3 the AEO or the polymerization degree and be 15 AEO, under the same conditions, prepare SiO with bar-shaped network structure
2Colloidal sol.
Embodiment 6
In the foregoing description 1, also can add the 10ml polymerization degree and be 3 the AEO or the polymerization degree and be 15 AEO, under the same conditions, prepare SiO with bar-shaped network structure
2Colloidal sol.
Embodiment 7
In the foregoing description 1, also can add 0.1ml multipolymer (PEO)
3-(PPO)
30-(PEO)
3Or multipolymer (PEO)
4-(PPO)
39-(PEO)
4, under the same conditions, prepare SiO with dendroid network structure
2Colloidal sol.
Embodiment 8
In the foregoing description 1, also can add 5ml multipolymer (PEO)
3-(PPO)
30-(PEO)
3Or multipolymer (PEO)
4-(PPO)
39-(PEO)
4, under the same conditions, prepare SiO with dendroid network structure
2Colloidal sol.
Embodiment 9
In the foregoing description 1, also can add 10ml multipolymer (PEO)
3-(PPO)
30-(PEO)
3Or multipolymer (PEO)
4-(PPO)
39-(PEO)
4, under the same conditions, prepare SiO with dendroid network structure
2Colloidal sol.
Claims (3)
1. a surficial modification process for SiO 2 sol particles comprises the steps:
(1) in half of the total consumption of ethanolic soln, adds tetraethoxy, whisk even back and form solution (I);
(2) quantitative water, ammoniacal liquor and additive are added in second half of the total consumption of ethanolic soln, mix the back and form solution (II);
(3) in whipping process, solution (II) is slowly added in the solution (I), continue to stir 30 minutes, then mixed solution is changed in the airtight molten device of tetrafluoroethylene over to constant temperature ageing, the SiO that promptly obtains having different spaces conformation network structure
2Colloidal sol;
The proportioning (mol ratio) that it is characterized in that colloidal sol is as follows:
Ethanol: water: additive: ammoniacal liquor: tetraethoxy=
(10-100)∶0.5-(10∶0.01)-0.1∶(1.0×10
-5)∶1；
2. a kind of surficial modification process for SiO 2 sol particles according to claim 1 is characterized in that 20-260 ℃ of described ageing temperature, digestion time 0.5 day-1 year.
3. a kind of surficial modification process for SiO 2 sol particles according to claim 1, it is characterized in that described additive can be polyoxyethylene glycol (PEG), Fatty Alcohol(C12-C14 and C12-C18) oxygen Vinyl Ether (AEO), fat is prevented pure polyoxyethylene poly-oxygen propylene aether multipolymer (PEO-PPO-PEO).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN98124657A CN1089077C (en) | 1998-11-04 | 1998-11-04 | Surficial modification process for SiO2 sol particles |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN98124657A CN1089077C (en) | 1998-11-04 | 1998-11-04 | Surficial modification process for SiO2 sol particles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1253117A true CN1253117A (en) | 2000-05-17 |
| CN1089077C CN1089077C (en) | 2002-08-14 |
Family
ID=5228740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN98124657A Expired - Fee Related CN1089077C (en) | 1998-11-04 | 1998-11-04 | Surficial modification process for SiO2 sol particles |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1089077C (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102807224A (en) * | 2011-06-05 | 2012-12-05 | 广州纳科米兹新材料有限公司 | Application of silica material with disordered microporous structure and long-chain alkyl groups |
| CN102807225A (en) * | 2011-06-05 | 2012-12-05 | 广州纳科米兹新材料有限公司 | Preparation of disordered porous silicon dioxide material and application of fatty alcohol-polyoxyethylene ether to preparation of disordered porous silicon dioxide material |
| CN103359954A (en) * | 2012-04-01 | 2013-10-23 | 比亚迪股份有限公司 | Preparation method of silicon dioxide super-hydrophobic thin film and super-hydrophobic material |
| CN103991876A (en) * | 2014-05-06 | 2014-08-20 | 上海大学 | Organically modified silica sol and preparation method thereof |
| CN106832417A (en) * | 2017-03-14 | 2017-06-13 | 北京化工大学 | Using aliphatic APEO modified white carbon black and its with rubber combined method |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4006392A1 (en) * | 1989-03-21 | 1990-09-27 | Cabot Corp | AQUEOUS COLLOIDAL DISPERSION FROM GAS PHASE-BASED SILICON DIOXIDE, FROM AN ACID AND FROM A STABILIZER, AND A METHOD FOR THEIR PRODUCTION |
| CN1062250C (en) * | 1995-11-14 | 2001-02-21 | 中国科学院大连化学物理研究所 | Method for in-situ dressing surface of sol particles |
| CN1155514A (en) * | 1996-01-25 | 1997-07-30 | 天津市化学试剂一厂 | Manufacture of high purity, high concentration and high granularity large granular silicon dioxide gel |
-
1998
- 1998-11-04 CN CN98124657A patent/CN1089077C/en not_active Expired - Fee Related
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102807224A (en) * | 2011-06-05 | 2012-12-05 | 广州纳科米兹新材料有限公司 | Application of silica material with disordered microporous structure and long-chain alkyl groups |
| CN102807225A (en) * | 2011-06-05 | 2012-12-05 | 广州纳科米兹新材料有限公司 | Preparation of disordered porous silicon dioxide material and application of fatty alcohol-polyoxyethylene ether to preparation of disordered porous silicon dioxide material |
| CN102807224B (en) * | 2011-06-05 | 2014-10-01 | 广州纳科米兹新材料有限公司 | Application of silica material with disordered microporous structure and long-chain alkyl groups |
| CN102807225B (en) * | 2011-06-05 | 2015-07-29 | 广州纳科米兹新材料有限公司 | Preparation and the fatty alcohol-polyoxyethylene ether of unordered porous silica silicon materials are applied in this preparation |
| CN103359954A (en) * | 2012-04-01 | 2013-10-23 | 比亚迪股份有限公司 | Preparation method of silicon dioxide super-hydrophobic thin film and super-hydrophobic material |
| CN103991876A (en) * | 2014-05-06 | 2014-08-20 | 上海大学 | Organically modified silica sol and preparation method thereof |
| CN103991876B (en) * | 2014-05-06 | 2016-11-02 | 上海大学 | Organically-modified silicon dioxide gel and preparation method thereof |
| CN106832417A (en) * | 2017-03-14 | 2017-06-13 | 北京化工大学 | Using aliphatic APEO modified white carbon black and its with rubber combined method |
| CN106832417B (en) * | 2017-03-14 | 2019-01-18 | 北京化工大学 | Use aliphatic APEO modified white carbon black and its method compound with rubber |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1089077C (en) | 2002-08-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Ju et al. | Continuous production of lignin nanoparticles using a microchannel reactor and its application in UV-shielding films | |
| CN108070368B (en) | Self-emulsifying emulsion and preparation method thereof | |
| CN103964448A (en) | Method for preparing monodisperse silicon dioxide nanoparticle sol for paint | |
| CN108114617B (en) | Small-particle-size ultralow-concentration nano emulsion composition and preparation method thereof | |
| CN108751208B (en) | Monodisperse silicon dioxide nanospheres prepared from surfactant-free microemulsion and preparation method thereof | |
| CN111204790B (en) | Method for preparing submicron spherical calcium carbonate based on reverse microemulsion | |
| CN1089077C (en) | Surficial modification process for SiO2 sol particles | |
| CN109879303A (en) | A kind of preparation method of the nanometer calcium carbonate of the dispersion of stable suspersion in aqueous solution | |
| CN109621851B (en) | Preparation method of gamma-valerolactone/glycerol system high-yield lignin micro-nanospheres | |
| CN102614857B (en) | Preparation method of metal ion dosed monodisperse mesoporous silicon dioxide spherical nanoparticles | |
| CN1120801C (en) | Dual-pore molecular sieve and its preparing process | |
| CN108299579A (en) | A kind of graphene/nanometer silica/Polystyrene Hybrid Material and its preparation method and application | |
| CN1853778A (en) | Synthesis of SBA-15-SO3II solid-phase catalyst and Beckmann rearrangement, esterification catalytic performances | |
| CN114956104B (en) | Silicon dioxide reinforcing agent for silicon rubber and preparation method thereof | |
| CN104609431A (en) | Synthetic method and particle size control synthetic method for SiO2 nano particles smaller than 50 nm | |
| CN102127286B (en) | New water-soluble epoxy emulsion and preparation method thereof | |
| CN1772607A (en) | Ultrasonic treating process of preparing spherical nanometer silica particle | |
| CN113185709A (en) | Pickering emulsion based on pineapple peel residue nanocellulose and preparation method thereof | |
| Ono et al. | Preparation of silica microcapsules by sol-gel method in W/O emulsion | |
| CN113136194B (en) | Emulsion based on nanocellulose and preparation method and application thereof | |
| CN114452227A (en) | Method for preparing alcohol-in-water-in-oil-in-water multiple pickering emulsion by anti-solvent recrystallization method | |
| CN112300768B (en) | Nanoparticle-reinforced residual oil emulsion profile control and flooding agent and preparation method thereof | |
| CN111646491B (en) | Dispersion liquid for dispersing nano particles in corona-resistant paint, preparation method and application thereof, and application of stable nano particle dispersion liquid | |
| CN113697850A (en) | Perovskite nanocrystalline powder capable of being dispersed by polar solvent and large-scale preparation method thereof | |
| CN114891517A (en) | Rosin-based CO 2 /N 2 Responsive microemulsion and preparation method and application thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C06 | Publication | ||
| PB01 | Publication | ||
| 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: 20020814 Termination date: 20111104 |