Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Organic-inorganic hybrid polymer and method of making same

a hybrid polymer and organic polymer technology, applied in the direction of synthetic resin layered products, coatings, transportation and packaging, etc., can solve the problems of reduced optical clarity, difficult to achieve good bonding, and inability to use lenses made of organic polymers, so as to achieve the effect of fast cure on the surface of plasti

Inactive Publication Date: 2002-09-12
JIN DAN L +1
View PDF0 Cites 29 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0026] A protective film in accordance with the present application has a very high density and a very high hardness to provide excellent abrasion and stain resistance. The high density and hardness are achieved by a high degree of cross linking between organic molecules and inorganic silica.
[0044] It is a further object of the invention to provide a composition that cures faster on plastic surfaces.

Problems solved by technology

However, the surfaces of the plastic materials used in ophthalmic lenses are relatively soft and porous compared to glass, and this frequently results in reduced optical clarity due to abrasion and staining of the lens surface.
Because thin films of these inorganic oxides are best applied in traditional processes that reach 1000.degree. C. or more, they cannot be used with lenses that are made of organic polymers which will decompose at such temperatures.
Inorganic oxides can be applied to organic polymers by such processes as chemical vapor deposition and the sol-gel process but it is difficult to achieve a good bond because of the inherent incompatibility between the inorganic coating and the organic substrate.
The different coefficients of thermal expansion for the inorganic coating and the organic substrate tend to cause delamination.
Inorganic films with sufficient thickness to adequately protect relatively soft plastic substrate surfaces may become brittle and are prone to crazing.
Equipment for chemical vapor deposition also requires a large capital investment and, because the necessary high vacuum chamber is relatively small, the numbers and sizes of articles that can be processed is limited.
In addition, the improvement in abrasion resistance does not approach the abrasion resistance provided by protective films of inorganic oxides.
The amount of silica that can be added to a coating material for ophthalmic lenses is limited by the requirements of avoiding agglomeration of silica particles and insuring good dispersion so that the silica particles will not be visible in the protective film.
These compositions do not have chemical bonding between the silica and the polymer, and protective thin film coatings formed with such compositions tend to fail in a relatively short time.
As previously mentioned, the silica particles sometimes become visible in the protective thin film coatings formed from the compositions or otherwise interfere with the optical clarity of the lenses on which the coatings are applied.
The relatively porous preformed silica particles also are relatively fragile and do not significantly alter the relatively soft nature of the plastic matrix.
However, methyl is an inert organic group that dramatically reduces the possible degree of crosslinking bonds.
Decreased crosslinking reduces the density of a film formed by the composition so that it remains relatively porous and does not have optimum hardness.
The absence of any curing compound also reduces the possible crosslinking reactions by silanol condensation and by ring opening polymerization of epoxy groups.
Thin film coatings formed by this composition also do not provide optimum abrasion resistance to the surface.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Organic-inorganic hybrid polymer and method of making same

Examples

Experimental program
Comparison scheme
Effect test

example i

[0069] A coating solution is prepared by mixing 104.0 g of tetraethyl orthosilicate, 45.0 g of glycidoxypropyltrimethoxysilane, 5.0 g methacryloxypropyltrimethoxysilane, 119.0 g of isopropyl alcohol, 43.0 g of water, 0.4 g of 2M HCl and 3.2 g of 2M acetic acid. The solution is stirred at room temperature to partially hydrolyze the silane groups until a clear solution is obtained. The solution is then heated up to and maintained at 60-70.degree. C. for 1-2 hours while continuing the stirring to completely hydrolyze all silane groups. The solution is then cooled to room temperature, followed by the addition of 1.6 g of Brij.RTM.98 surfactant and 1.2 g of aluminum acetylacetonate catalyst. The solution then is stirred to dissolve the solids, and to obtain a homogeneous and clear solution.

[0070] A CR-39 lens is cleaned dried and immersed into the coating solution and withdrawn edgewise with the lens surfaces generally perpendicular to the solution surface at a rate of 5-15 cm / min. In th...

example ii

[0074] A scratch resist coating solution is prepared by mixing 313 g of tetraethyl orthosilicate, 200 g of glycidoxypropyltrimethoxysilane, 40 g methacryloxypropyltrimethoxysilane, 472 g of isopropyl alcohol, 144 g of water, 1.2 g of 2M HCl and 10.8 g 2M HAc. The solution is stirred at room temperature to partially hydrolyze the silane groups until a clear solution is obtained. The solution is then heated up to and maintained at 60-70.degree. C. for 1-2 hours while continuing the stirring to completely hydrolyze all silane groups. The solution is then cooled to room temperature followed by the addition of 6.0 g of Brij.RTM.98 surfactant and 4.0 g of aluminum acetylacetonate catalyst. The solution is then stirred to dissolve the solids, and obtain a homogeneous and clear solution.

[0075] A CR-39 lens is cleaned, dried and immersed into the coating solution followed by withdrawal edgewise with the lens surfaces generally perpendicular to the solution surface at a rate of 5-15 cm / min. T...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
weight percentaaaaaaaaaa
weight percentaaaaaaaaaa
weight percentaaaaaaaaaa
Login to View More

Abstract

An optically clear protective thin film having covalent chemical bonds on a molecular level between organic polymer and in situ generated silica molecules is formed from a hydrolyzed coating solution of tetraalkyl orthosilicate, epoxyalkylalkoxy silanes, (math)acryloxyalkylalkoxy silanes and solvent.

Description

RELATED APPLICATIONS[0001] This application is a division of copending U.S. Serial No. 09 / 870,221 filed May 30, 2001 which is a division of copending U.S. Ser. No. 09 / 528,276 filed Mar. 17, 2000.BACKGROUND OF THE INVENTION[0002] This application relates to the art of compositions and, more particularly, to an organic-inorganic hybrid polymer composition and a method of making same. The invention is particularly applicable to compositions for applying optically clear protective thin films to the surfaces of plastic eyeglass lenses and will be described with specific reference thereto. However, it will be appreciated that the invention has broader aspects and that the composition can be used for other purposes as well as for coating other plastic substrate surfaces, such as transparent display cases, windows and crystals for covering faces of clocks, watches and other instruments.[0003] Plastic materials commonly are used for ophthalmic lenses because they are lighter, easier to proce...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): B32B27/08C09D4/00C09D183/06C09D183/14
CPCB32B27/08C09D4/00C09D183/06C09D183/14C08G77/20C08G77/02Y10T428/31507Y10T428/31663Y10T428/249978Y10T428/31667Y10T428/249979Y10T428/26
Inventor JIN, DAN L.SINGH, BRIJ P.
Owner JIN DAN L
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products