CN100363437C - Method for preparing silicon-titanium micro-coarse structured hydrophilic film - Google Patents
Method for preparing silicon-titanium micro-coarse structured hydrophilic film Download PDFInfo
- Publication number
- CN100363437C CN100363437C CNB2006100489333A CN200610048933A CN100363437C CN 100363437 C CN100363437 C CN 100363437C CN B2006100489333 A CNB2006100489333 A CN B2006100489333A CN 200610048933 A CN200610048933 A CN 200610048933A CN 100363437 C CN100363437 C CN 100363437C
- Authority
- CN
- China
- Prior art keywords
- titanium
- acid
- sol
- film
- hydrophilic film
- 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
- UGACIEPFGXRWCH-UHFFFAOYSA-N [Si].[Ti] Chemical compound [Si].[Ti] UGACIEPFGXRWCH-UHFFFAOYSA-N 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 title abstract description 7
- 239000002253 acid Substances 0.000 claims abstract description 18
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 17
- 150000001282 organosilanes Chemical class 0.000 claims abstract description 13
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 12
- 239000010936 titanium Substances 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000002904 solvent Substances 0.000 claims abstract description 9
- 239000008367 deionised water Substances 0.000 claims abstract description 8
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 5
- DCKVFVYPWDKYDN-UHFFFAOYSA-L oxygen(2-);titanium(4+);sulfate Chemical compound [O-2].[Ti+4].[O-]S([O-])(=O)=O DCKVFVYPWDKYDN-UHFFFAOYSA-L 0.000 claims abstract description 5
- 229910000348 titanium sulfate Inorganic materials 0.000 claims abstract description 5
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 claims abstract description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- 229910052710 silicon Inorganic materials 0.000 claims description 10
- 239000010703 silicon Substances 0.000 claims description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 9
- 230000001476 alcoholic effect Effects 0.000 claims description 8
- 238000007669 thermal treatment Methods 0.000 claims description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- 238000013019 agitation Methods 0.000 claims description 6
- 238000005507 spraying Methods 0.000 claims description 6
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 5
- 239000011707 mineral Substances 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 229960000935 dehydrated alcohol Drugs 0.000 claims description 4
- 238000003618 dip coating Methods 0.000 claims description 4
- 238000004528 spin coating Methods 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 229910017604 nitric acid Inorganic materials 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 2
- 230000001105 regulatory effect Effects 0.000 claims description 2
- 239000011521 glass Substances 0.000 abstract description 10
- 239000004033 plastic Substances 0.000 abstract description 5
- 229920003023 plastic Polymers 0.000 abstract description 5
- 239000012780 transparent material Substances 0.000 abstract description 5
- 150000001875 compounds Chemical class 0.000 abstract description 4
- 238000010438 heat treatment Methods 0.000 abstract description 3
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 238000003756 stirring Methods 0.000 abstract 2
- 238000005299 abrasion Methods 0.000 abstract 1
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000011259 mixed solution Substances 0.000 abstract 1
- 239000010408 film Substances 0.000 description 38
- 229910010413 TiO 2 Inorganic materials 0.000 description 10
- 238000009736 wetting Methods 0.000 description 10
- 230000000694 effects Effects 0.000 description 5
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- LYCAIKOWRPUZTN-NMQOAUCRSA-N 1,2-dideuteriooxyethane Chemical compound [2H]OCCO[2H] LYCAIKOWRPUZTN-NMQOAUCRSA-N 0.000 description 1
- 101100203596 Caenorhabditis elegans sol-1 gene Proteins 0.000 description 1
- 229920000604 Polyethylene Glycol 200 Polymers 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 230000001443 photoexcitation Effects 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000005320 surfactant adsorption Methods 0.000 description 1
- 210000001138 tear Anatomy 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 230000003245 working effect Effects 0.000 description 1
Landscapes
- Surface Treatment Of Glass (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
The present invention relates to a preparing method for a film, which aims to provide a preparing method for a hydrophilic film with a silicon-titanium micro coarse structure. The preparing method provided by the present invention comprises the following steps: at least one of titanium tetrachloride, titanium sulfate or butyl titanate is added in alcohol solvent under the condition of stirring to obtain primary titanium sol; (2) the mixed solution of deionized water and acid is dripped in organosilane under the condition of stirring to obtain organosilicone sol; (3) the primary titanium sol is mixed with the organosilicone sol to obtain compound sol; (4) the compound sol is filmed on the surface of a base plate to obtain the hydrophilic film with the silicon-titanium micro coarse structure via heat treatment after film formation. The film of the present invention can be widely appled to transparent material such as glass, plastics, etc., has super hydrophilicity (can prevent can prevent fog) under the irradiation of light rays, can keep the hydrophilicity for a long time, and has good abrasion resistance.
Description
Technical field
The present invention relates to a kind of preparation method of film, more particularly, the present invention relates to a kind of preparation method of silicon-titanium micro-coarse structured hydrophilic film.
Background technology
Rain or wet weather, especially in the winter time with last month of spring in autumn at the beginning of the time, on glass, plastics such as building window, automobile weatherstrip window, glasses, bathroom, can form droplet.These transparent materials do not cause the globule to adhere to because the surface is not hydrophilic.Glass or frosting haze, and be light then make troubles for people's life, and as in the winter of cold, ophthalmic lens can be atomized in the outdoor inlet chamber, influences people's vision; Heavy then the life security that jeopardizes the people influences sight line as atomizing on automobile rearview mirror or the front windshield.
The surface of hydrophilization can make the water droplet or the mist pearl drawout of surface in contact, is tiled into the moisture film of layer of transparent, thereby eliminates the sight line influence.For this reason, the research and development hydrophilic film becomes the problem that Chinese scholars is paid close attention to.Main research concentrates on tensio-active agent, hydrophilic high mol, inorganic semiconductor aspect; In addition, the microtexture of film has a significant impact wetting ability.
Have and adopt the surfactant-based hydrophilic report of glass that carries out, generally be with SURFACTANT ADSORPTION at glass or frosting, perhaps sneak into plastics inner and constantly move to the surface again.Mainly be that hydrophilic radical in the abutment surface active agent molecule works, water droplet filming that will contact glass; But tensio-active agent can in use run off, can only the short-term onset, and generally in a week.
Other has and adopts hydrophilic macromolecule to carry out the film forming report of transparent material surface, and hydrophilic time apparent surface promoting agent can prolong, but anti-fog effect is general, and the wear resistance of organic film is relatively poor, weares and teares easily and influences transmittance, and work-ing life is limited.
More promising hydrophilic research concentrates on inorganic semiconductor TiO
2, SiO
2Deng film.The wear resistance of inorganic thin film is all fine, and groundwork concentrates on and improves on its wetting ability.
TiO
2Have photic Superhydrophilic, and can do very thinly and transparent, so can be widely used on the transparent materials such as glass, plastics.TiO
2The limitation of hydrophilic film is: its wetting ability comes from photoexcitation, when film loses irradiate light, can slowly lose wetting ability.Discover, with SiO
2And TiO
2After compound, film surface also can be kept long-time wetting ability in the dark.
The microtexture of film has a significant impact the hydrophilicity on surface.Coarse structures such as the hole of micro-nano-scale, hole, wetting ability that can enhanced film.Existing research adopts PEG at TiO
2Vesicular structure is constructed in the burning volatilization in the sintering process, increases TiO
2The wetting ability of film.
Summary of the invention
The objective of the invention is to overcome deficiency of the prior art, the preparation method of the persistent silicon-titanium micro-coarse structured hydrophilic film of a kind of hydrophilic effect is provided.
The preparation method of silicon-titanium micro-coarse structured hydrophilic film provided by the invention may further comprise the steps:
(1) under agitation condition with in the wherein at least a adding alcoholic solvent of titanium tetrachloride, titanium sulfate or butyl (tetra) titanate, regulating pH value with acid is 2~5, obtains titanium colloidal sol just; Alcoholic solvent is 1~5 with the molar mass ratio that adds material;
(2) under agitation condition, in organosilane, splash into deionized water and sour mixing solutions; Wherein, deionized water is 0.1~1 with the molar mass ratio of organosilane, and acid is 0.001 with the molar mass ratio of organosilane; Dripping acid again, to regulate pH value be 2~5, obtains molecular weight and be 1000~5000 organic silicon sol;
(3) be that 1: 0.1~2 ratio is mixed with aforementioned first titanium colloidal sol and organic silicon sol with pH value in the mole mass ratio, obtain complex sol;
(4) with complex sol at substrate surface with spin coating, dip-coating or spraying method film forming, film forming is after 300~600 ℃ of thermal treatment 0.5~2 hour obtains silicon-titanium micro-coarse structured hydrophilic film.
As a kind of improvement of the present invention, described alcoholic solvent is wherein one or more the combination of dehydrated alcohol, ethylene glycol, Virahol.
As a kind of improvement of the present invention, described acid is that mineral acid or organic acid are wherein at least a.
As a kind of improvement of the present invention, described mineral acid is wherein a kind of or wherein several combination of nitric acid, hydrochloric acid, sulfuric acid
As a kind of improvement of the present invention, described organic acid is an acetate.
Compared with prior art, the invention has the beneficial effects as follows:
Among the present invention, organosilane is hydrolysis-polymerization in reaction process, formation has the organism of certain molecular weight, can play two effects in heat treatment process: the organic carbochain in its molecule can be burnt and be volatilized with gas form, it is coarse to form surface microscopics such as hole, hole at film surface, improves the wetting ability of film from microtexture; Finally generate SiO on the other hand after the silane thermal treatment
2, with TiO
2The compound stability that can improve hydrophilic effect.Film among the present invention can be widely used in possessing Superhydrophilic (can be antifog) under irradiate light, and keeping for a long time on the transparent materials such as glass, plastics, has good wear resistance simultaneously.
Embodiment
Below the present invention is further described by example.
It is as follows that the present invention prepares among the embodiment of silicon-titanium micro-coarse structured hydrophilic film operation steps:
(1) under agitation condition, in the alcoholic solvent with wherein at least a adding of titanium tetrachloride, titanium sulfate or butyl (tetra) titanate 1~5 times (m/m), is 2~5, obtains titanium colloidal sol just with acid adjusting pH value;
(2) under agitation condition, in organosilane, splash into the mixing solutions of deionized water [consumption is 0.1~1 times (m/m) of organosilane] and small amount of acid [0.001 times (m/m) of the about organosilane of consumption], dripping acid again, to regulate pH value be 2~5, obtains molecular weight and be 1000~5000 organic silicon sol;
(3) aforementioned first titanium colloidal sol and organic silicon sol with pH value is mixed in 1: 0.1~2 ratio (m/m), obtain complex sol;
(4) with complex sol at substrate surface with spin coating, dip-coating or spraying method film forming, film forming is after 300~600 ℃ of thermal treatment 0.5~2 hour obtains silicon-titanium micro-coarse structured hydrophilic film.
Described alcoholic solvent is wherein one or more the combination of dehydrated alcohol, ethylene glycol, Virahol.
Described acid can be wherein a kind of or wherein several combinations of organic acid such as mineral acids such as nitric acid, hydrochloric acid, sulfuric acid or acetate.
Testing data among each embodiment as follows.
Select silane coupling agent KH560 and butyl (tetra) titanate for use, its consumption is according to SiO in the final laminated film
2/ TiO
2Than being calculating in 1: 2; Prepare organic silicon sol and titanium colloidal sol respectively, and keep pH value 3.5, two component colloidal sols are incorporated in the glass surface film forming again, film is handled 30min at 600 ℃, the purer TiO2 film of the laminated film wetting ability of acquisition is better.
Shown in the embodiment of titanium colloidal sol configuration just saw the following form, except that pH value, other numerical value was the mass ratio relation in the table.
The specific embodiment sequence number | X1 | X2 | X3 | X4 | X5 | X6 | X7 |
Titanium tetrachloride | 1 | 0.5 | 0.5 | 0.3 | |||
Titanium sulfate | 1 | 0.5 | 0.5 | 0.4 | |||
Butyl (tetra) titanate | 1 | 0.5 | 0.5 | 0.3 |
Dehydrated alcohol | 1 | 2 | 2 | 2 | |||
Ethylene glycol | 2 | 2 | 2 | 1.5 | |||
Virahol | 3 | 2 | 2 | 1.5 | |||
PH value | 2 | 2.5 | 3 | 3.5 | 4 | 4.5 | 5 |
Shown in organic silicon sol configuration embodiment saw the following form, the numerical value of deionized water and organosilane was the mass ratio relation in the table, and molecular weight is to be the gel chromatography measurement result of standard specimen with PEG200.
The specific embodiment sequence number | Y1 | Y2 | Y3 | Y4 | Y5 |
Organosilane | 1 | 1 | 1 | 1 | 1 |
Deionized water | 0.1 | 0.3 | 0.5 | 0.75 | 1 |
PH value | 2 | 3 | 3.5 | 4 | 5 |
Molecular weight Z | 1000 | 3000 | 3500 | 4000 | 5000 |
Complex sol and laminated film prepare shown in embodiment sees the following form, in the table just the numerical value of titanium colloidal sol and organic silicon sol be that mass ratio concerns.
The specific embodiment sequence number | Z1 | Z2 | Z3 | Z4 | Z5 |
PH value | 2 | 3 | 3.5 | 4 | 5 |
First titanium colloidal sol | 1 | 1 | 1 | 1 | 1 |
Organic silicon sol | 0.1 | 0.3 | 0.5 | 1 | 2 |
Thin film-forming method | Spraying | Dip-coating | Spraying | Spin coating | Spraying |
Thermal treatment temp ℃ | 300 | 400 | 500 | 550 | 600 |
Heat treatment time h | 0.5 | 1 | 1 | 1.5 | 2 |
Get silicon titanium amount ratio in the film, and factors such as thermal treatment temp and time, final hydrophilic influence sees the following form to film.
Numbering | SiO 2/TiO 2 | Thermal treatment temp | Soaking time | The water droplet spreading area (cm * cm) |
X0 | Pure TiO 2 | 600℃ | 30min | 1.8×2.0 |
X1 | 1/1 | 500℃ | 30min | 0.8×0.8 |
X2 | 1/1 | 500℃ | 2h | 0.9×0.7 |
X3 | 1/1 | 600℃ | 30min | 1.2×1.1 |
Y1 | 1/2 | 500℃ | 30min | 1.5×1.5 |
Y2 | 1/2 | 500℃ | 2h | 1.5×1.6 |
Y3 | 1/2 | 550℃ | 30min | 1.7×1.8 |
Y4 | 1/2 | 600℃ | 30min | 2.2×2.5 |
SiO
2When content increased, laminated film takes the lead in improving the back to the utilization of light to be reduced, and correspondingly hydrophilicity also improves afterwards earlier and reduces.Along with the raising of thermal treatment temp, the corresponding enhancing of the wetting ability of laminated film; But when prolonging soaking time, the hydrophilic effect of laminated film changes and is not obvious.
At last, it is also to be noted that what more than enumerate only is specific embodiments of the invention.Obviously, the invention is not restricted to above examples of implementation, many distortion can also be arranged.All distortion that those of ordinary skill in the art can directly derive or associate from content disclosed by the invention all should be thought protection scope of the present invention.
Claims (5)
1. the preparation method of a silicon-titanium micro-coarse structured hydrophilic film may further comprise the steps:
(1) under agitation condition with in the wherein at least a adding alcoholic solvent of titanium tetrachloride, titanium sulfate or butyl (tetra) titanate, regulating pH value with acid is 2~5, obtains titanium colloidal sol just; Alcoholic solvent is 1~5 with the molar mass ratio that adds material;
(2) under agitation condition, in organosilane, splash into deionized water and sour mixing solutions; Wherein, deionized water is 0.1~1 with the molar mass ratio of organosilane, and acid is 0.001 with the molar mass ratio of organosilane; Dripping acid again, to regulate pH value be 2~5, obtains molecular weight and be 1000~5000 organic silicon sol;
(3) be that 1: 0.1~2 ratio is mixed with aforementioned first titanium colloidal sol and organic silicon sol with pH value in the mole mass ratio, obtain complex sol;
(4) with complex sol at substrate surface with spin coating, dip-coating or spraying method film forming, film forming is after 300~600 ℃ of thermal treatment 0.5~2 hour obtains silicon-titanium micro-coarse structured hydrophilic film.
2. the preparation method of hydrophilic film according to claim 1 is characterized in that, described alcoholic solvent is wherein one or more the combination of dehydrated alcohol, ethylene glycol, Virahol.
3. the preparation method of hydrophilic film according to claim 1 is characterized in that, described acid is that mineral acid or organic acid are wherein at least a.
4. the preparation method of hydrophilic film according to claim 3 is characterized in that, described mineral acid is wherein a kind of or wherein several combination of nitric acid, hydrochloric acid, sulfuric acid.
5. the preparation method of hydrophilic film according to claim 3 is characterized in that, described organic acid is an acetate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2006100489333A CN100363437C (en) | 2006-01-06 | 2006-01-06 | Method for preparing silicon-titanium micro-coarse structured hydrophilic film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2006100489333A CN100363437C (en) | 2006-01-06 | 2006-01-06 | Method for preparing silicon-titanium micro-coarse structured hydrophilic film |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1803940A CN1803940A (en) | 2006-07-19 |
CN100363437C true CN100363437C (en) | 2008-01-23 |
Family
ID=36866093
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2006100489333A Expired - Fee Related CN100363437C (en) | 2006-01-06 | 2006-01-06 | Method for preparing silicon-titanium micro-coarse structured hydrophilic film |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN100363437C (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10231344B2 (en) | 2007-05-18 | 2019-03-12 | Applied Nanotech Holdings, Inc. | Metallic ink |
US9730333B2 (en) | 2008-05-15 | 2017-08-08 | Applied Nanotech Holdings, Inc. | Photo-curing process for metallic inks |
CN101747670B (en) * | 2008-11-28 | 2012-03-07 | 富港电子(东莞)有限公司 | Preparation method of composite paint and product thereof |
KR101735710B1 (en) | 2009-03-27 | 2017-05-15 | 어플라이드 나노테크 홀딩스, 인크. | Buffer layer to enhance photo and/or laser sintering |
CN102114419B (en) * | 2009-12-30 | 2013-01-30 | 比亚迪股份有限公司 | Preparation method of photocatalysis and transmission increasing sol and glass coating material |
WO2014011578A1 (en) | 2012-07-09 | 2014-01-16 | Applied Nanotech Holdings, Inc. | Photosintering of micron-sized copper particles |
CN112358761B (en) * | 2020-10-20 | 2023-08-11 | 广东环境保护工程职业学院 | Modified nano ceramic slurry, water-based paint, and preparation method and application thereof |
CN113025103A (en) * | 2021-03-16 | 2021-06-25 | 北京石油化工学院 | Multi-effect antibacterial and antiviral film layer and preparation method thereof |
CN113264689A (en) * | 2021-03-30 | 2021-08-17 | 新沂市铭达玻璃有限公司 | Anti-fogging toughened glass for vehicle and manufacturing process thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1248561A (en) * | 1999-09-02 | 2000-03-29 | 吉林大学 | Compound mass sol-gel preparation process |
CN1546781A (en) * | 2003-12-05 | 2004-11-17 | 东华大学 | Composite hydrosol color fixing finishing agent, synthesizing method and use thereof |
CN1548403A (en) * | 2003-05-09 | 2004-11-24 | 山 汪 | Protecting composite membrane and its prepn |
-
2006
- 2006-01-06 CN CNB2006100489333A patent/CN100363437C/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1248561A (en) * | 1999-09-02 | 2000-03-29 | 吉林大学 | Compound mass sol-gel preparation process |
CN1548403A (en) * | 2003-05-09 | 2004-11-24 | 山 汪 | Protecting composite membrane and its prepn |
CN1546781A (en) * | 2003-12-05 | 2004-11-17 | 东华大学 | Composite hydrosol color fixing finishing agent, synthesizing method and use thereof |
Also Published As
Publication number | Publication date |
---|---|
CN1803940A (en) | 2006-07-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN100363437C (en) | Method for preparing silicon-titanium micro-coarse structured hydrophilic film | |
EP1689824B1 (en) | Silica films and method of production thereof | |
US6337301B1 (en) | Photocatalytic metal oxide composition, thin film, and composite | |
CN101631745B (en) | Silica porous body, laminate and composition for optical use, and method for producing silica porous body | |
KR101799121B1 (en) | Method for structuring a surface by means of reactive ion-beam etching, structured surface and uses | |
CN101203581A (en) | Control of morphology of silica films | |
CN102898036B (en) | Preparation method of super-hydrophilic thin film based on glass surface | |
KR20120117997A (en) | Method for structuring a surface by means of ion-beam etching, structured surface and uses | |
CN110272211B (en) | Method for preparing silicon dioxide/titanium dioxide composite film containing dendritic pore structure on substrate | |
CN101786801A (en) | Super-hydrophilic anti-fog anti-reflection coating and preparation method and application thereof | |
WO2010018852A1 (en) | Coating compositions and articles with formed coating films | |
JP2004511418A (en) | Safety glass with wear-resistant porous SiO2 anti-reflective coating | |
KR20080106510A (en) | Coating system | |
CN103333600A (en) | Preparation method for one-component waterborne polyurethane transparent heat-insulating coating | |
CN111057998B (en) | Super-hydrophilic anti-fog coating and preparation method and application thereof | |
CN104761153A (en) | Super-hydrophilic anti-fog coating for glass and preparation method thereof | |
KR101069316B1 (en) | Functional coating composition for preventing contamination and coating method using the same | |
US9012354B2 (en) | Photocatalytic film, method for forming photocatalytic film and photocatalytic film coated product | |
CN108516697A (en) | Super-hydrophilic anti-reflection coating, preparation method and glass | |
CN100363454C (en) | Production of antifogging and abrasive coating solution of spectacle lens | |
CN103553361B (en) | A kind of Al 2o 3-SiO 2-TiO 2the preparation method of inorganic anti-reflection film | |
CN108947265B (en) | Glass self-cleaning liquid, self-cleaning glass and preparation method thereof | |
JP5071277B2 (en) | Low reflection member and manufacturing method | |
JP3865589B2 (en) | Method for forming colored film | |
CN116004071B (en) | Water-based anti-fog self-cleaning automobile glass paint and preparation method thereof |
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 | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20080123 Termination date: 20130106 |