CN101671354A - Method for preparing release agent - Google Patents
Method for preparing release agent Download PDFInfo
- Publication number
- CN101671354A CN101671354A CN200910190333A CN200910190333A CN101671354A CN 101671354 A CN101671354 A CN 101671354A CN 200910190333 A CN200910190333 A CN 200910190333A CN 200910190333 A CN200910190333 A CN 200910190333A CN 101671354 A CN101671354 A CN 101671354A
- Authority
- CN
- China
- Prior art keywords
- parts
- solution
- preparation
- remover
- grating
- 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
Abstract
The invention discloses a method for preparing release agent, and the release agent is prepared by silane coupling agent monomer through hydrolytic condensation reaction. The silane coupling agent monomer can be 4-methyl-(perfluoroalkyl hexyl ethyl) propyl trimethoxy silane or tetraethoxysilane. A Mould modified by the release agent prepared by the method can be used for manufacturing a micro-lensarray grating, and the manufactured grating has good appearance, has no phenomenon of burr, orange peel, water wave, uneven photo-permeability and the like, and can meet the requirement of producingthe high quality grating.
Description
Technical field
The present invention relates to a kind of preparation method of releasing agent.
Background technology
In stereo display technique, especially in the bore hole stereo display technique, the use of microlens array grating more and more widely, the production technique of microlens array grating also reaches its maturity and is various, and the technology that especially adopts UV to solidify glue (UV-irradiation curing glue) production microlens array grating more and more receives publicity and develops.The UV cured adhesive is by prepolymer, reactive monomer, and principal constituents such as light trigger are equipped with auxiliary agents such as stablizer, flow agent and form.It is under the UV rayed of suitable wavelength, and light trigger generates free radical or ion rapidly, causes prepolymer and reactive monomer polymerization crosslinking and reticulates structure, glues the bonding of material thereby finish with quilt.
On the slightly concave array mold, can prepare dimpling lens arra grating, on dimpling shape array mold, can prepare nick lens arra grating, the material of mould can be metal (copper, iron, tin etc.) in the preparation, also can be that UV solidifies glue material (Resins, epoxy, polyester, urethane etc.), perhaps organic polymer (polymethylmethacrylate, polyvinyl alcohol, polystyrene etc.).Below the method for making nick lens arra grating in the prior art is elaborated.
Making method comprises the steps:
Step 1: coating UV is solidified glue on mould.UV is solidified glue to be coated on the column dimpling shape array mold, on solidifying glue, UV covers base materials such as one deck PET (polyethylene terephthalate) material or glass, smooth by roll squeezer or the laminating machine roll extrusion of adjusting spacing, unnecessary glue amount is extruded; Make UV solidify glue nature levelling through the suitable UV roller coating machine of spacing after also UV can being solidified the glue coating.
Step 2: ultraviolet light polymerization.The dimpling shape array mold that coating is finished is placed in the oxygen-free environment, as nitrogen environment etc., makes UV solidify adhesive curing with ultra violet lamp.
Step 3: the demoulding.Just peel off, can also can obtain column nick lens arra grating by mechanically peel by manual removal.
In order can intactly to peel off, before making grating, need carry out modification to the surface of mould and handle, change the performance of die surface, make grating break away from and be more prone to from mould.Present modification mode is surface coating and uses remover that the advantage of surface coating is that the grating surface pattern that makes is good.But the coating temperature height makes that easily mould deforms, and protruding grating and most concave(diffraction)grating narrow for arch span and that sagitta is big are inapplicable, and the demoulding number of times of making grating is limited, and the technology cost is more high.It is cheap using the advantage of remover, and all gratings all are suitable for, and the demoulding number of times is than adopting the many of plated film.But also can produce grating smoothly behind the at present commercially available remover modification mould, but that the sub-gratings that makes can occur is scared, orange peel, water wave, printing opacity are inhomogeneous etc., can not satisfy application.
Summary of the invention
The object of the present invention is to provide the preparation method of the better releasing agent of a kind of modified effect with low cost, the releasing agent that this method obtains can remedy the deficiency of existing releasing agent.
In order to realize purpose of the present invention, the spy provides a kind of preparation method of remover, adopts the silane coupling agent monomer to be prepared through hydrolysis-condensation reaction.
Described silane coupling agent monomer can be 4-methyl-(perfluoro hexyl ethyl) propyl trimethoxy silicane, and concrete preparation process is as follows:
1) 4-methyl-(perfluoro hexyl ethyl) propyl trimethoxy silicane and 15 parts of deionized waters of measuring 1 part of purity 96% respectively with graduated cylinder are mixed in the round-bottomed flask;
2) add magnetic stir bar and start magnetic agitation and solution was mixed in 2 minutes, this moment, solution was muddy state;
3) drip acidic solution in flask and make solution pH value to 3.0 between 4.0, add 16 parts of dehydrated alcohols then, reflux obtains water white remover after 24 hours.
Described silane coupling agent monomer can also be tetraethoxy, and concrete preparation process is as follows:
1) measures 7 parts of dehydrated alcohols respectively with graduated cylinder and 3 parts of deionized waters are mixed in the round-bottomed flask, add magnetic stir bar and also start magnetic agitation;
2) drip 8 parts of tetraethoxys in flask, drip acidic solution again and make pH value to 3.0 between 4.0 in flask, stirring reaction obtained colourless transparent solution after 5 hours under the room temperature;
3) with this colourless transparent solution uniform mixing in the solvent of forming by 200 parts of ethanol and 2000 parts of deionized waters, stirred 1 hour, promptly obtain remover.
Described acidic solution can be Glacial acetic acid or hydrochloric acid.
To be used on the microlens array preparing grating through the mould of the releasing agent modification of method for preparing, the grating surface pattern that makes is good, and it is inhomogeneous etc. scared, orange peel, water wave, printing opacity can not to occur, can satisfy the requirement of production high-quality grating.
Description of drawings
Do not have
Embodiment
The be hydrolyzed method of condensation reaction of silane coupling agent monomer is all adopted in the preparation of remover among the present invention.The embodiment of the invention has been enumerated and has been utilized two kinds of silane coupling agent monomers to prepare the method for releasing agent, and two kinds of silane coupling agent monomers are respectively 4-methyl-(perfluoro hexyl ethyl) propyl trimethoxy silicane and tetraethoxy, describe respectively below.
(1) utilize 4-methyl-(perfluoro hexyl ethyl) propyl trimethoxy silicane to prepare the method for remover
1) 4-methyl-(perfluoro hexyl ethyl) propyl trimethoxy silicane and the 150ml deionized water of measuring 10ml purity 96% respectively with graduated cylinder is mixed in the round-bottomed flask;
2) add magnetic stir bar and start magnetic agitation and solution was mixed in 2 minutes, this moment, solution was muddy state;
3) drip Glacial acetic acid or hydrochloric acid conditioning solution pH value to 3.0 between 4.0 in flask, add the 160ml dehydrated alcohol then and do solubilizing agent, heating reflux reaction obtained colourless transparent solution after 24 hours, was remover.
In the aforesaid method, the ratio of 4-methyl-(perfluoro hexyl ethyl) propyl trimethoxy silicane, deionized water and dehydrated alcohol is 1: 15: 16.
(2) utilize tetraethoxy to prepare the method for remover
1) measures the 7ml dehydrated alcohol respectively with graduated cylinder and the 3ml deionized water is mixed in the round-bottomed flask, add magnetic stir bar and also start magnetic agitation;
2) drip the 8ml tetraethoxy in flask, drip and drip Glacial acetic acid or hydrochloric acid conditioning solution pH value to 3.0 between 4.0 in flask, stirring reaction obtained colourless transparent solution after 5 hours under the room temperature;
3) this solution is evenly splashed in the solvent of forming by 200ml ethanol and 2000ml deionized water, stirred 1 hour, promptly obtain remover.
After making above-mentioned releasing agent, to treat that the modification mould is immersed in the remover of the above-mentioned 4-of utilization methyl-(perfluoro hexyl ethyl) propyl trimethoxy silicane preparation, soak after 0.5 minute and take out, vertically put into 60 ℃ constant temperature electric heating air dry oven along mould gully direction, place 0.5-1.5 hour post-modification process and finish.Storage period, length was decided according to the pitch of mould, and pitch is more little, in requisition for modification time long more.
For the above-mentioned remover that utilizes the tetraethoxy preparation, to treat that equally the modification mould soaks wherein taking-up after 0.5 minute, mould gully, room temperature lower edge direction is vertically placed, the post-modification process was finished in time 1-3 days, storage period, length was decided according to the pitch of mould, pitch is more little, in requisition for modification time long more.
To be used in through the mould of above-mentioned modification in the preparing grating process, the grating surface pattern that makes is good.It is inhomogeneous etc. scared, orange peel, water wave, printing opacity can not to occur, can satisfy the requirement of production high-quality grating.Those skilled in the art will envision that, be not limited to the preparation of grating, can also be used for the field that other adopts mould to produce according to the application of the releasing agent of the present invention preparation.And being not limited to above-mentioned two kinds of silane coupling agent monomers, other silane coupling agent monomer can obtain identical effect equally.
The present invention prepares the remover that is fit to the die surface modification, and mould can unlimited preparation grating after surface modification and the surface topography of grating is bright and clean, printing opacity is even, can satisfy application.
Above-mentioned embodiment only is schematic; rather than restrictive, those skilled in the art is not breaking away under the scope situation that present method aim and claim protect under the enlightenment of present method; can also make a lot of distortion, these all belong within protection scope of the present invention.
Claims (5)
1, a kind of preparation method of remover is characterized in that, adopts the silane coupling agent monomer to be prepared through hydrolysis-condensation reaction.
2, the preparation method of remover according to claim 1 is characterized in that, described silane coupling agent monomer is 4-methyl-(perfluoro hexyl ethyl) propyl trimethoxy silicane, and concrete preparation process is as follows:
1) 4-methyl-(perfluoro hexyl ethyl) propyl trimethoxy silicane and 15 parts of deionized waters of measuring 1 part of purity 96% respectively with graduated cylinder are mixed in the round-bottomed flask;
2) add magnetic stir bar and start magnetic agitation and solution was mixed in 2 minutes, this moment, solution was muddy state;
3) drip acidic solution in flask and make solution pH value to 3.0 between 4.0, add 16 parts of dehydrated alcohols then, reflux obtains water white remover after 24 hours.
3, the preparation method of remover according to claim 1 is characterized in that, described silane coupling agent monomer is a tetraethoxy, and concrete preparation process is as follows:
1) measures 7 parts of dehydrated alcohols respectively with graduated cylinder and 3 parts of deionized waters are mixed in the round-bottomed flask, add magnetic stir bar and also start magnetic agitation;
2) drip 8 parts of tetraethoxys in flask, drip acidic solution again and make pH value to 3.0 between 4.0 in flask, stirring reaction obtained colourless transparent solution after 5 hours under the room temperature;
3) with this colourless transparent solution uniform mixing in the solvent of forming by 200 parts of ethanol and 2000 parts of deionized waters, stirred 1 hour, promptly obtain remover.
According to the preparation method of claim 2 or 3 described removers, it is characterized in that 4, described acidic solution is a Glacial acetic acid.
According to the preparation method of claim 2 or 3 described removers, it is characterized in that 5, described acidic solution is a hydrochloric acid.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2009101903334A CN101671354B (en) | 2009-09-17 | 2009-09-17 | Method for preparing release agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2009101903334A CN101671354B (en) | 2009-09-17 | 2009-09-17 | Method for preparing release agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101671354A true CN101671354A (en) | 2010-03-17 |
| CN101671354B CN101671354B (en) | 2012-06-27 |
Family
ID=42018797
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2009101903334A Active CN101671354B (en) | 2009-09-17 | 2009-09-17 | Method for preparing release agent |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN101671354B (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108312396A (en) * | 2018-01-31 | 2018-07-24 | 漳州丰笙新材料有限公司 | A kind of silicon mould release and preparation method thereof |
| CN110383113A (en) * | 2017-03-07 | 2019-10-25 | 日本板硝子株式会社 | The manufacturing method of optical component and optical component |
| CN114106601A (en) * | 2021-12-30 | 2022-03-01 | 上海中化科技有限公司 | Stripping coating composition and method for preparing polyimide film by using same |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2681847B2 (en) * | 1990-12-28 | 1997-11-26 | 大日精化工業株式会社 | Release treatment agent |
| JP2003236819A (en) * | 2001-12-11 | 2003-08-26 | Asahi Kasei Corp | Mold release agent for form, and form |
-
2009
- 2009-09-17 CN CN2009101903334A patent/CN101671354B/en active Active
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110383113A (en) * | 2017-03-07 | 2019-10-25 | 日本板硝子株式会社 | The manufacturing method of optical component and optical component |
| US11041991B2 (en) | 2017-03-07 | 2021-06-22 | Nippon Sheet Glass Company, Limited | Optical component and method of manufacturing optical component |
| CN108312396A (en) * | 2018-01-31 | 2018-07-24 | 漳州丰笙新材料有限公司 | A kind of silicon mould release and preparation method thereof |
| CN108312396B (en) * | 2018-01-31 | 2021-10-26 | 漳州丰笙新材料有限公司 | Silicon release agent and preparation method thereof |
| CN114106601A (en) * | 2021-12-30 | 2022-03-01 | 上海中化科技有限公司 | Stripping coating composition and method for preparing polyimide film by using same |
| CN114106601B (en) * | 2021-12-30 | 2022-12-13 | 上海中化科技有限公司 | Stripping coating composition and method for preparing polyimide film by using same |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101671354B (en) | 2012-06-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN104789039B (en) | A kind of interior raw type frosting effect glass ink and the method that frosting effect product is produced using it | |
| CN103476804B (en) | The manufacture method of active energy ray-curable resin composition, molding, minute concave-convex structure body, water repellency article, mould and minute concave-convex structure body | |
| CN101303421B (en) | Method for manufacturing microlens array | |
| CN101934267B (en) | Preparation method of self-supporting colloid photon crystal film | |
| CN101738860B (en) | For the photosensitive resin composition of imprint process and the method for forming organic layer on substrate | |
| CN101602913A (en) | A kind of ultraviolet light curing anti fogging coating composite and compound method thereof | |
| CN102061127A (en) | UV-solidified nanometer inorganic/organic hybrid painting preparation method and application thereof | |
| CN103554540A (en) | Hardening film for in-mold decoration | |
| CN101671354B (en) | Method for preparing release agent | |
| CN101289891A (en) | Light cured fluorine carbon veneer polyurethane thermal insulation board and its manufacturing technique | |
| CN106125172A (en) | A kind of diffusion barrier and preparation method thereof | |
| CN102232014B (en) | Shaping method | |
| CN105754391B (en) | A kind of located laser soft mode version photocureable coating and preparation method | |
| JP2023063316A (en) | Light extraction member | |
| CN103113822A (en) | Ultraviolet light curable coating with dewdrop effect and preparation method and coating method thereof | |
| KR101271981B1 (en) | Method for manufacturing texture steel sheet using uv radiation coating and texture steel sheet menufactured with the method | |
| CN1047351C (en) | Decorative imitation jade material, its preparing method and use | |
| CN104974309A (en) | Ultraviolet Curable Resin Composition | |
| CN106956437A (en) | A kind of method for improving 3D printing transparent material surface translucency | |
| CN101011908A (en) | Agate imitation and jade imitation calligraphy and painting and manufacturing method thereof | |
| CN105549135B (en) | Brightness enhancement film, its preparation method and include its display device | |
| CN101768401A (en) | Manufacturing method of low-temperature curing electrophoretic coating | |
| CN114809510B (en) | Irreversible temperature change ceramic tile composite board | |
| CN108342106A (en) | A kind of decoration thin aluminium photocuring white coating and its preparation and application method | |
| CN103232740B (en) | A kind of photocuring application composition for preparing high-ductility optical grade cured film and corresponding cured film |
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 | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20180803 Address after: 518000 Room 201, building A, No. 1, Qian Wan Road, Qianhai Shenzhen Hong Kong cooperation zone, Shenzhen, Guangdong (Shenzhen Qianhai business secretary Co., Ltd.) Patentee after: Shenzhen super Technology Co., Ltd. Address before: 518000 A-03, 2 storey west seat 10, Sai tech Industrial Park, Huaqiang North Road, Futian District, Shenzhen, Guangdong Patentee before: Shenzhen SuperD Photoelectronic Co., Ltd. |
|
| TR01 | Transfer of patent right |