AU680231B2 - Light valve suspensions and films containing UV absorbers and light valves containing the same - Google Patents
Light valve suspensions and films containing UV absorbers and light valves containing the same Download PDFInfo
- Publication number
- AU680231B2 AU680231B2 AU59381/94A AU5938194A AU680231B2 AU 680231 B2 AU680231 B2 AU 680231B2 AU 59381/94 A AU59381/94 A AU 59381/94A AU 5938194 A AU5938194 A AU 5938194A AU 680231 B2 AU680231 B2 AU 680231B2
- Authority
- AU
- Australia
- Prior art keywords
- light valve
- suspension
- liquid
- benzotriazole derivative
- light
- 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
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- 239000000725 suspension Substances 0.000 title claims description 93
- 239000006096 absorbing agent Substances 0.000 title claims description 23
- 239000007788 liquid Substances 0.000 claims description 101
- 229920000642 polymer Polymers 0.000 claims description 55
- 239000002245 particle Substances 0.000 claims description 51
- 239000011159 matrix material Substances 0.000 claims description 35
- 239000003381 stabilizer Substances 0.000 claims description 32
- 150000001565 benzotriazoles Chemical class 0.000 claims description 30
- 239000007787 solid Substances 0.000 claims description 17
- 230000003019 stabilising effect Effects 0.000 claims description 13
- 239000012964 benzotriazole Substances 0.000 claims description 8
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical class C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 238000011160 research Methods 0.000 claims description 2
- 210000002421 cell wall Anatomy 0.000 claims 6
- FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical class OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 claims 2
- 238000005054 agglomeration Methods 0.000 claims 2
- 230000002776 aggregation Effects 0.000 claims 2
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims 1
- 230000005855 radiation Effects 0.000 description 20
- 239000000463 material Substances 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 11
- 239000006194 liquid suspension Substances 0.000 description 9
- 230000000087 stabilizing effect Effects 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 229920006037 cross link polymer Polymers 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 150000003797 alkaloid derivatives Chemical class 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 4
- 239000000020 Nitrocellulose Substances 0.000 description 4
- 229930013930 alkaloid Natural products 0.000 description 4
- 210000004027 cell Anatomy 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- QTMDXZNDVAMKGV-UHFFFAOYSA-L copper(ii) bromide Chemical compound [Cu+2].[Br-].[Br-] QTMDXZNDVAMKGV-UHFFFAOYSA-L 0.000 description 4
- -1 e.g. Substances 0.000 description 4
- 230000005684 electric field Effects 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 229920001220 nitrocellulos Polymers 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- 241000894007 species Species 0.000 description 4
- OOHZIRUJZFRULE-UHFFFAOYSA-N 2,2-dimethylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(C)C OOHZIRUJZFRULE-UHFFFAOYSA-N 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical class C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 description 3
- 238000002835 absorbance Methods 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- XQAABEDPVQWFPN-UHFFFAOYSA-N octyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCCCCCCCC)=CC(N2N=C3C=CC=CC3=N2)=C1O XQAABEDPVQWFPN-UHFFFAOYSA-N 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- OCLTZILENWBWIY-HKPQTANOSA-N (r)-[(2s,4s,5r)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol;molecular iodine;sulfuric acid;dihydroiodide Chemical compound I.I.II.II.OS(O)(=O)=O.OS(O)(=O)=O.OS(O)(=O)=O.C([C@H]([C@H](C1)C=C)C2)CN1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21.C([C@H]([C@H](C1)C=C)C2)CN1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21.C([C@H]([C@H](C1)C=C)C2)CN1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21.C([C@H]([C@H](C1)C=C)C2)CN1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 OCLTZILENWBWIY-HKPQTANOSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910021590 Copper(II) bromide Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 239000011358 absorbing material Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- RJIFVNWOLLIBJV-UHFFFAOYSA-N tributyl benzene-1,2,4-tricarboxylate Chemical compound CCCCOC(=O)C1=CC=C(C(=O)OCCCC)C(C(=O)OCCCC)=C1 RJIFVNWOLLIBJV-UHFFFAOYSA-N 0.000 description 2
- 125000005591 trimellitate group Chemical group 0.000 description 2
- 210000000635 valve cell Anatomy 0.000 description 2
- WFJNHVWTKZUUTR-KODHJQJWSA-N (r)-[(2s,4s,5r)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-quinolin-4-ylmethanol Chemical compound C1=CC=C2C([C@@H](O)[C@@H]3C[C@@H]4CCN3C[C@@H]4CC)=CC=NC2=C1 WFJNHVWTKZUUTR-KODHJQJWSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- JEEQUUSFXYRPRK-UHFFFAOYSA-N 3,6-dimethyloctane Chemical compound CCC(C)CCC(C)CC JEEQUUSFXYRPRK-UHFFFAOYSA-N 0.000 description 1
- UWSMKYBKUPAEJQ-UHFFFAOYSA-N 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O UWSMKYBKUPAEJQ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 241000233805 Phoenix Species 0.000 description 1
- 206010042496 Sunburn Diseases 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- JIONYXURSFWPTK-UHFFFAOYSA-N [Ca].N1=C(C(=NC=C1)C(=O)O)C(=O)O Chemical compound [Ca].N1=C(C(=NC=C1)C(=O)O)C(=O)O JIONYXURSFWPTK-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- OCWYEMOEOGEQAN-UHFFFAOYSA-N bumetrizole Chemical compound CC(C)(C)C1=CC(C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O OCWYEMOEOGEQAN-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003413 degradative effect Effects 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 229920000359 diblock copolymer Polymers 0.000 description 1
- WFJNHVWTKZUUTR-UHFFFAOYSA-N dihydrocinchonidine Natural products C1=CC=C2C(C(O)C3CC4CCN3CC4CC)=CC=NC2=C1 WFJNHVWTKZUUTR-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 230000005670 electromagnetic radiation Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N ferric oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 239000002223 garnet Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical class OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- 125000005375 organosiloxane group Chemical group 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- 229960001463 quinine bisulfate Drugs 0.000 description 1
- RONWGALEIBILOG-VMJVVOMYSA-N quinine sulfate Chemical compound [H+].[H+].[O-]S([O-])(=O)=O.C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21.C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 RONWGALEIBILOG-VMJVVOMYSA-N 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical class OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- UQMOLLPKNHFRAC-UHFFFAOYSA-N tetrabutyl silicate Chemical compound CCCCO[Si](OCCCC)(OCCCC)OCCCC UQMOLLPKNHFRAC-UHFFFAOYSA-N 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- WRTMQOHKMFDUKX-UHFFFAOYSA-N triiodide Chemical compound I[I-]I WRTMQOHKMFDUKX-UHFFFAOYSA-N 0.000 description 1
- 239000000326 ultraviolet stabilizing agent Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
Description
AUISTRAL IA Patents Act 1990 COMPLETE SPECIFICATION STANDARD PATENT 9 9#9*#9 o 9 99 49 0 99 94 94 9 9 #9*9 94 4. 9 99 9 9 0*9 4 9994 .499 9*94 09 9 4*9* 44.4 9009 99 4 44 4 44 9 #4.99.
S
Applicant: RESEARCH FRONTIERS INCORPORATED Invention Title: LIGHT VALVE SUSPENSIONS AND FILM4S CONTAINING UV ABSORBERS AND LIGH4T VALVES CONTAINING THE SAM'E C 2 p The following statement is a full description of this invention, including the best method of performing it known to me/us:
L
1A LIGHT VALVE SUSPENSIONS AND FILM CONTAINING UV ABSORBERS AND LIGHT VALVES CONTAINING THE SAME Field of the Invention The present invention relates to fluid suspensions for light valves and more particularly to methods and materials for stabilising liquid suspensions and films thereof from ultraviolet radiation.
Background Light valves have been used for almost 60 years Sfor modulation of light. A light valve may be described as a cell formed of two walls that are spaced apart by a "small distance, at least one wall being transparent, the 20 walls having electrodes thereon usually in the form of transparent electrically conductive coatings. The cell contains a "light valve suspension" which may be either a liquid light valve suspension or a film containing droplets of a liquid light valve suspension as described 25 hereinafter. iThe liquid light valve suspension comprises a plurality of small particles suspended in a r liquid suspending medium. In the absence of an applied electrical field, the particles in the liquid :.ght valve suspension exhibit random Brownian movement, and S, 30 hence a beam of light passing into the cell is reflected, transmitted or absorbed, depending upon the S"nature and concentration of the particles and the energy F content of the light. When an electric field is applied S\\HELB01\home\Sue\Keep\59381.95.speci.light.doc 21/04/97 y r j i 99 *L 9Q 0n 0o 0t oO 0ug 0e S S r 2 through the light valve suspension in the light valve, the particles become aligned and for many suspensions most .of the light can pass through the cell. Light valves have been proposed for many purposes including eg. alphanumeric displays, television displays, windows, mirrors, filters, ski goggles, eyeglasses and the like to control the amount of light passing therethrough.
Alternatively, in place of the liquid light valve suspension described above, one may use in the light valve a film comprising a polymer matrix having droplets of a liquid suspension distributed throughout the polymer matrix, such as is described in the aforesaid US patent Nos 5,463,491 and 5,463,492. All of the patents and patent applications referred to in this specification are incorporated herein by reference thereto. For more details, see the section, infra, entitled "Light Valve films".
i 7 eJ 9
S
S.
\\HELBOI\home-\\ue\Keep\593BI.95.speci.iightldoc 21/04/97
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The Licht Valve Suspension The light valve suspension of the present invention may be any liquid light valve suspension comprising droplets of a liquid light value suspension for a light valve known in the art or known to the inventors of the present invention or hereafter known and may be formulated according to known techniques. The term "light valve liquid suspension" or "liquid suspension" as used herein means a "liquid suspending °o medium" in which a plurality of small particles are dispersed.
The "liquid suspending medium" comprises one or more nonaqueous, electrically resistive liquids in which there is preferably dissolved at least one type of polymeric stabilizer which acts to reduce the tendency of the particles to agglomerate and acts to keep them dispersed.
As is known, inorganic and organic particles may be used in a light valve suspension, such as mica, metals, graphite, e o "d metal halides, polyhalides (sometimes referred to in the prior art as perhalides) of alkaloid acid salts and the like. The particles in the liquid suspension may I-e light-polarizing, such as halogen-containing light-polarizing materials, e.g., polyhalides of alkaloid acid salts. (The term "alkaloid" is used herein to mean an organic nitrogenous base, as defined in Hackh's Chemical Dictionary, Fourth Edition, McGraw-Hill 3 Book Company, New York, 1969). If a polyhalide of an alkaloid acid salt is used, the alkaloid moiety may be quinine alkaloid, as defined in Hackh's Chemical Dictionary, supra.
U.S. Patents 2,178,996 and 2,289,712 refer in detail to the use of polyhalides of quinine alkaloid acid salts. The particles may be light-absorbing or light-reflecting.
Also, the particles may be particles of a hydrogenated polyhalide of a quinine alkaloid acid salt, such as dihydrocinchonidine bisulfate polyiodide, as described in U.S.
Patent 4,131,334, or a light-polarizing metal halide or o o polyhalide, such as cupric bromide or purpureocobaltchloride i sulfate polyiodide, as, in U.S. Patent 1,956,867.
Preferably, the particles are light-polarizing polyhalide particles such as those described in U.S. Patent Nos.
4,877,313 and 5,002,701 which are more environmentally stable than prior art polyhalides.
Ogg4 In theory, any type of particle capable of reflecting, absorbing and/or transmitting de-ired wavelengths of visible light can be used in the light valve suspension.
The shape of the particles used in the light valve suspension should preferably be "anisometric", i.e. the shape or structure of the particle is such that in one orientation the particle intercepts more light than in another 4 1* Vc.
I
c ft ft ft ft.
oc L o *e o 8 o 0 oo «c aa or o 0t ft ft ftf ft ft ft o «1 no a 0 1 t f f ft f orientation. Particles which are needle-shaped, rod-shaped, lath-shaped, or in the form of thin flakes, are suitable.
The particles are preferably of colloidal size, that is the particles will have a large dimension averaging about 1 micron or less. It is preferred that most particles have large dimensions less than one-half of the wavelength of blue light, i.e. 2000 Angstroms or less to keep light scatter extremely low.
Any type of particle which when in suspension is orientable in an electric or magnetic field is usable including both light-scattering and light-absorbing particles.
However, particles that absorb visible light that impinges on them are preferred because they exhibit very little light scatter, and light-polarizing crystals are especially preferred and useful because they produce a pleasing visual appearance.
Light-absorbing particles comprise many types of material including colored orientable pigments and dyes, e.g. garnet red, conductive black or grey material such as graphite or carbon black, dichroic dyes such as are widely used in guesthost liquid crystal devices, light-polarizing materials, e.g., cupric bromide, and polyhalides, and especially polyiodides, those described in conjunction with prior art light 2 5 r 1 :25 1 valve devices.
I0 a o 1 .o 6 o« 00 90 9 6 0 9o99 99« I, a f o o 9 99 9 2* 99 0 9 9 9 9 9 9 9 Kk jI The term "polyiodide" as used herein is used in the conventional sense and also in the same sense as the term "periodide" is used in numerous prior art light valve patents, see column 1 of U.S. Patent 1,951,664 (Land) entitled "Colloidal Suspensions and the Process of Making Same," to indicate a material which is a reaction product of a precursor compound, which may be a sulfate (or certain other salts as described in U.S. Patent 4,270,841) of heterocyclic nitrogenous bases with iodine and an iodide. Such reaction products are often called polyiodide compounds. This type of particle is discussed in detail in "The Optical Properties and Structure of Polyiodides" by D.A.
Godina and G.P. Faerman published in The Journal of General Chemistry, U.S.S.R. Vol. 20, pp. 1005-1016, (1950).
Herapathite, for example, is quinine bisulfate polyiodide, and its formula is given under the heading "quinine iodosulfate" as 4C 20
H
24
N
2 0 2 .3H 2
SO,
4 .2HI.I,.6HO in The Merck Index, 10th Ed.
(Merck Co., Inc., Rahway, In more modern, preferred types of polyiodides, the precursor compound need not be a salt, see U.S. Patents Nos. 4,877,313 and 5,002,701.
In these polyiodide compounds the iodine is thought to form chains and the compounds are strong light polarizers. The term "polyhalide" is used herein to mean a compound such as a polyiodide, but wherein at least some of the iodine in the 6 1~ 41 iodide is replaced by another halogen element.
The light valve suspension of the present invention may include any of the liquid suspending media previously proposed for use in light valves for suspending the particles. In general, the liquid suspending medium may comprise one or more electrically resistive, chemically inert liquids that will both suspend the particles and dissolve any polymeric stabilizer used to reduce the tendency of the particles to agglomerate and thus keep the particles in suspension. Liquid suspending media that are known in the art are useful herein, .9 e such as the liquid suspending media disclosed in U.S. Patent 4,247,175. In general, one or both of the liquid suspending medium or the polymeric stabilizer dissolved therein is chosen so as to maintain the suspended particles in gravitational equilibrium.
A light valve suspension useful in the present invention is described in U.S. Patent 4,407,565 and is based upon the 26"' use as the liquid suspending medium of an electrically 0 9 resistive, chemically inert, low molecular weight liquid fluorocarbon polymer having a specific gravity at room temperature of at Jeast about 1.5 and having at least about of its atoms constituted by halogen atoms, at least of the halogen atoms being fluorine and the balance chlorine and/or bromine. Preferably, the liquid suspending medium also 7 Scomprises a miscible electrically resistive organic liquid such as, for example, trialkyl trimellitate, etc. to provide gravitational equilibrium to the suspended particles and to assist in dispersing the particles in the liquid suspending medium. Other materials useful as the miscible electrically resistive organic liquid are those disclosed in U.S. Patent 4,772,103, and details concerning the liquid suspending material may be found in U.S. Patent 4,407,565.
i19... Other types of light valve suspensions which do not 0 incorporate such halogenated liquids can also be used and can maintain the particles in gravitational equilibrium if a sufficient quantity of stabilizing polymer, is employed therein.
So. oAnother useful light valve suspension is based on the use as the liquid suspending medium of non-volatile or minimally to seoo o.o volatile organic liquids, commonly classified as plasticizers.
Such "plasticizer" liquid suspending media may comprise one or more electrically resistive, chemically inert, relatively
W
non-volatile (high boiling) organic liquids that will suspend the particles and will dissolve the polymeric stabilizer. For example, where the polymeric stabilizer of a liquid light valve suspension includes a solid poly(meth)acrylate, useful liquid suspending media include liquid plasticizers for poly(meth)acrylates, such as adipates, benzoates, glycerol 8 triacetate, isophthalates, mellitates, oleates, chloroparaffins, phthalates, sebacates and the like. Liquid suspending media for other solid polymeric stabilizers may be similarly selected form liquids useful as plasticizers for such polymers. Preferably, trialkyltrimellitates, such as tri-n-propyl-or tri-n-butyl-trimellitate and/or dialkyl adipates, such as di-2-ethylhexyl adipate, may be used as the liquid suspending medium for solid polymeric stabilizers based on copolymers of neopentyl(meth)acrylate.
°o The polymeric stabilizer when employed, can be a single type of solid polymer that bonds to the surface of the @0 0 particles but also dissolves in the non-aqueous liquid or liquids of the liquid suspending medium. Alternatively, there may be two or more solid polymeric stabilizers serving as a 0900 polymeric stabilizer system. For example, the particles can be coated with a first type of solid polymeric stabilizer such 0 .o as nitrocellulose, which in effect, provides a plain surface coating for the particles and one or more additional types of solid polymeric stabilizer that bond to or associate with the first type of solid polymeric stabilizer and also dissolve in the liquid suspending medium to provide dispersion and steric protection for the particles.
Preferably, to keep the particles in suspension, the liquid suspending medium may also comprise as the solid 9 i polymeric stabiliser an A-B type block copolymer as disclosed in European Patent Publication 350,354.
Nitrocellulose and/or other solid polymeric stabilisers may also be usefully provided in the liquid suspending medium in addition to the block polymer. It is preferred to use just enough A-B block polymer to maintain the particles in suspension, the amount to be used for a given light valve suspension being empirically determined, as is known. Usually, theJ amount of the solid polymeric stabiliser will be from about 1% to about 30%, such as from 5% to about 25%, by weight, based on the total weight of the light valve liquid suspension. However, while the use of a solid polymeric stabiliser is preferred, it need not be used in all cases. Indeed, liquid polymeric stabilisers may be used to advantage, as described in the aforesaid patent applications relating to films usable in light valves.
.'Light Valve Films While the liquid light valve suspension can be used as such as the light-modulating element of a light 4 f ~,*valve, it is also possible to use as the lightmodulating element a film having droplets of a liquid light valve suspension distributed in a polymer matrix.
See US Patents 3,257,905, 3,341,274 and 4,919,521 and United States Patent Nos 5,463,491 and 5,463,492 which are incorporated herei,n by reference thereto.
'T \\MELB01\home$\U\KeeP\9g1.95sPeci~lightdoc 21/04/97 Thus, a film suitable for use in a light valve may comprise a cross-linked polymer matrix having droplets of a light valve suspension distributed in the matrix, the light valve suspension comprising particles suspended in a liquid suspending medium. The particles exhibit random Brownian movement in the absence of an electric field applied to the light valve suspension and become aligned in the presence of an electric field applied to the light valve suspension.
The film of the cross-linked polymer matrix having droplets of a light valve suspension distributed therein may be swollen with a suitable liquid. This improves the -v frequency response characteristics of the' resulting film and reduces light scatter.
In a preferred embodiment of the invention, the crosslinked polymer matrix is a cross-linked polyorganosiloxane.
When the film is formed from a liquid cross-linkable I A Spolyorganosiloxane oligomer or polymer, it is preferred to S emulsify a liquid cross-linkable polyorganosiloxane oligomer *or polymer and a liquid light valve suspension with an organosiloxane/organic monomer copolymer as emulsifier, a o ii ora emlsf af .;udcoslnkbeplognsioaeoio y- -ll-IT-- followed by treating a thin layer of the emulsion to crosslink the cross-linkable polyorganosiloxane oligomer or polymer, thereby forming the film.
A film suitable for use as the light modulating element' of a light valve may also comprise a cross-linked polymer matrix that contains functional groups soluble in the liquid light valve suspension. In particular, the polymer matrix may be provided by a liquid cross-linkable copolymer emulsifier that includes such functional groups. The film may be formed 9 by providing an emulsion of the liquid light valve suspension in a liquid cross-linkable copolymer emulsifier, followed by a cross-linking reaction. The liquid cross-linkable copolymer emulsifier not only provides the cross-linked polymer matrix, but also acts as an emulsifier in forming the film.
M The film may also comprise a cross-linked oo. polyorganosiloxane polymer matrix and the liquid light valve suspension distributed in the cross-linked polymer matrix may include a partially or fully fluorinated polymeric stabilizer, whereby the light scatter or "haze" of the light valve film is substantially reduced. Further improvements in the reduction of the haze may be obtained by providing the crosslinked polyorganosiloxane polymer matrix with aromatic groups and/or by swelling the film with a partially or fully fluorinated organic liquid. As used herein, the term 12
T
|i "f 13 "fluorinated" means a partially or fully fluorinated material.
Ultraviolet Radiation and UV Absorbers jli 0 0 90f 9e a 00 oQ a o a 9 0 99090 09 4 D O C 0OD 0 9 9 a9*9 9 09 B 099 o« o 6 o 6 9 oo 9 9 r r As used herein, the ultraviolet (UV) region of the electromagnetic spectrum comprises electromagnetic radiation having a wavelength in the range of about 100 Angstroms to about 4,000 Angstroms. Such UV radiation can be dangerous, especially to the eyes, but can also cause sunburn and can degrade many types of materials. As a result, it is very often important to block or absorb UV radiation in order to prevent or lessen such problems.
As is true for many materials, light valve suspensions are susceptible to degradation by ultraviolet radiation such as UV radiation from sunlight. Exposure of a light valve film and/or a light valve suspension to UV radiation can eventually lead to adverse changes in the suspension, such as color change and/or reduction in the contrast ratio for a given applied voltage. Because many of the applications of light valves involve exposing the light valve and the liquid light valve suspension therein to UV radiation, it is very important to reduce the degradative effect of such radiation on the light valve suspension. One can, of course, deposit a single or multilayer coating known in the art that absorbs or reflects ultraviolet radiation on the outside wall of a light 13
IF
e:1 valve. Interception of UV radiation by such coating will reduce the amount of UV radiation reaching the light valve suspension inside the light valve and therefore be beneficial.
However, such a coating may require a substantial expense that one would prefer to avoid.
Ultraviolet absorbers, sometimes referred to in the art as ultraviolet stabilizers, are substances that absorb radiant 1( energy in the ultraviolet region of the electromagnetic spectrum. There are many known types of UV absorbers.
Benzophenones are a widely used class of UV absorber.
However, they generally have limited solubility in low polarity aliphatic liquids, and hence are not well suited for use in light valve suspensions. Other classes of possible UV I absorbers such as phenol-nickel complexes are also not well ~suited for use in light valve suspensions because of factors such as poor solubility, too high electrical conductivity in some cases, or poor compatibility with the suspended particles.
Summary Of The Invention In order to obtain the benefits of a good UV absorber while avoiding the problems associated with most types of UV stabilizers, we have found that UV absorbers of the class known as substituted or unsubstituted 2-(2'-hydroxyphenyl)- 14 -t 15 benzotriazoles meet the requirements of light valve suspensions excellently. (For convenience, these UV absorbers will be referred to herein as "benzotriazole derivatives") According the one aspect of the present invention there is provided a liquid light valve suspension comprising particles suspended in a liquid suspending medium, in which the liquid suspending medium has dissolved therein a UV-absorbing effective amount of a substituted or unsubstituted 2-(2'-hydroxyphenyl)- i benzotriazole.
Liquid or solid benzotriazole derivatives can be -a dissolved in the liquid suspending medium of a liquid light valve suspension before or after the liquid light valve *20 2 0 suspension is made. When the benzotriazole derivative is a o highly miscible liquid, this can be particularly advantageous because the UV absorber can then comprise a substantial part of the liquid light valve suspension and thus be highly 25 effective in preventing or reducing UV degradation of the SOre light valve suspension. It is preferred that such a liquid benzotriazole derivative be non-volatile or of very low volatility so as to have very low vapor pressure and, if used in a film for a light valve, remain in'the film.
H!\SUe\Keep\59J81.95.speci.light.doc 21/04/97 i 1 SI 1 1O 16 t j 04 flt I 09 4E oi a Od ;J 00~ 94
I
4 10 .4- Pal 4JJ a aDJ uJ 4 Ga 4 Cl The several ways in which a UV stabiliser may be incorporated into a film containing droplets of a liquid. For instance, the UV stabiliser may be dissolved in a swelling agent used to treat the film and so be introduced into the film. See US patent No 5,463,491. Or the UV stabiliser may be added to the liquid light valve suspension before mixing with the matrix polymer. Or the UV stabiliser may be mixed with the polymer matrix. Or the UV stabiliser may be incorporated directly into the polymer matrix (by substituting, for example, UV absorber molecules for some of the methyl groups in the polydimethylsiloxane polymer or other such substitution in other matrix polymers). Or the UV stabiliser may be directly incorporated into the stabilising polymer via derivatisation of a UV stabiliser to a reactive monomer, and subsequent co-polymerisation to yield the 20 stabilising polymer.
Monomers comprising benzotriazole derivatives can be conveniently used as comonomers in the stabilising polymer of a liquid suspension and/or as part of the structure of a matrix polymer used in a film form of the fluid suspension.
In another embodiment, the stabilising polymer or the matrix polymer. contains reactable groups which 30 are reacted with the UV absorbing material of the benzotriazole derivatives, which have in their structure a group that will react with and bond to the reactable groups in the matrix polymer or stabilising polymer.
It should be noted that when a light valve is \\MELBB1\homeS\Sue\Keep\59381.95.specid.ight.doc 21/04/97 4 most UV radiation, the value of the light valve may be greatly enhanced because it can prevent objects on one side of the sight valve from being degraded by UV radiation such as sunlight, which impinges on the light valve from the other side.
The present invention thus provides a liquid light valve suspension stabilized against exposure to ultraviolet radiation by including in the liquid light valve suspending medium of the light valve suspension an effective amount of a solid or liquid benzotriazole derivative.
S
L The present invention also provides a liquid light valve 2 suspension stabilized against exposure to UV radiation by incorporating into the polymeric stabilizer of the liquid light valve suspension copolymerized units of a monomer which comprises a UV-absorbing group, such as a benzotriazole 2 derivative, in a UV-stabilizing effective amount.
25 o0 u 3 u The present invention also provides a UV-stabilized film for use as the light-modulating element of a light valve by S* 0 using as a swelling agent for the film an effective amount of a liquid benzotriazole dervative and/or by incorporating into the matrix polymer of the film an effective amount of copolymerized units of a benzotriazole derivative.
r< H:\Sue\leep\59a61.95.speci.light.doc 21/04/97 Detailed Description Of The Invention The benzotriazole derivatives useful in the present invention include those having the formula (1)
HO
N N R
N
wherein RI, R 2 and R 3 are independently hydrogen, halogen or an organic group. Where the benzotriazole is used as a 00 comonomer, as described above, R, or R 2 will be an organic S• group having a polymerizable double bond, preferably a terminal polymerizable double bond. Suitably, R 3 is hydrogen, halogen, preferably chlorine, alkyl or alkoxy. Suitably, the 19"' organic group having a terminal polymerizable double bond may be derived from acrylic acid or methacrylic acid or esters or S amides thereof.
0 Ciba-Geigy Corporation sells benzotriazole derivatives 2cr:'" for use as UV absorbers under the registered trademark TINUVIN. These benzotriazoles have the formula above.
In Tinuvin 327, for example, R, and R 2 ale each tertiary butyl and R, is chlorine. In Tinuvin 328, each of R 2 and R 2 is a S, C(CH 3 2
CH
2
CH
3 group and R 3 is hydrogen. In Tinuvin 326 R, is tertiary butyl, R, is methyl and R 3 is chlorine. In Tinuvin P, Ri and R3 are each hydrogen and R 2 is methyl. All four of S18 j r p 00000 100 O 0.
0 00 0*~ 0 0 000 0 r 0 0* 0 000tr *000 00 these compounds are solid powders at room temperature.
Although all four of these compounds are soluble in some organic liquids, Tinuvin 328 is the most soluble in low polarity organic liquids and therefore, of this group, is most useful when dissolved in the liquid suspending medium of a light valve suspension or dissolved directly into the suspension itself.
Liquid benzotriazole derivatives are also known. For example, Tinuvin 384 is a liquid. Tinuvin 384 is of formula I, wherein RI is tertiary butyl, R 2 is -CHCH 2 COOCeH,, and R 3 is hydrogen.
The greater the solubility of the UV absorber in the suspension, the more of it that can be put safely in the suspension without the risk of precipitation of the material, especially at cold temperatures, and the better the suspension will be protected from UV radiation. Also, the more UV radiation is absorbed by the suspension in a light valve, the more effective the light valve will be in preventing rugs, upholstery, paintings, etc., from being degraded by UV radiation when the light valve is used as a window.
It is also possible to greatly improve the stability of a light valve suspension to UV radiation by incorporating a UV-absorbing compound either in the polymeric stabilizer of 1 2 5 1
I
r r 9*9999 o :9 99 9 99 o the liquid suspension or in the matrix polymer of a light valve film.
Rigorous UV tests were performed on the liquid light valve suspensions and films described in the Examples using as the UV source equipment sold by Heraeus DSET Laboratories, Inc. of Phoenix, Arizona under the name "Suntest CPS." This equipment puts out between 400 and 765 watts per square meter of total irradiance below 800nm, and was operated at maximum power for the tests described below.
Example 1 A liquid light valve suspension in a light valve cell was subjected to the UV source for 605 hours. The suspension comprised 2.5% paste (comprising particles of acid calcium polyiodide coated with nitrocellulose polymer), 20.5% tri-n-butyl trimellitate, 3.16% of a stabilizing polymer which was an A- B block copolymer of neopentylmethacrylate/hydroxyethylmethacrylate having a number average molecular weight of about 309,000 and monomer units of hydroxyethyl methacrylate, 69.84% Halocarbon Oil Type 0.8 (sold by Halocarbon Products, Hackensack, New Jersey) and 4% Tinuvin 328. After exposure to the UV source for 605 hours, no substantial change in either color or absorbance was observed.
p .1i
U
i i i L I *1 150#
K
.00.
a a a a.
2 0a 0 )I 200* Example 2 A film was made by combining, emulsifying and crosslinking with heat 2.07 g. of dihydroxy-terminated polydimethylsiloxane having a molecular weight of about 150,000 with 0.04 g. of tetrabutylorthosilicate, 0.05 g. of dibuty t i ndi l aurate 0 2 g. of a polydimethylsiloxane/neopentylmethacrylate block copolymer emulsifier and 0.74 g. of a particle concentrate. The concentrate was a viscous concentrated liquid suspension comprising 20% paste (comprising particles of pyrazine dicarboxylic acid calcium polyiodide coated with nitrocellulose polymer), 20% of an A-B block stabilizing copolymer of neopentyl methacrylate/hydroxyethylmethacrylate having a .umber average molecular weight of about 349,000 and only 8 hydroxyethylmethacrylate monomeric units, and 60% of tri-npropyl trimellitate plasticizing liquid. The crosslinked film was swollen with a 10% solution of Tinuvin 328 in 3,6dimethyloctane. The swollen film was placed in a light valve cell and exposed to the UV source for 575 hours with no substantial change in either the color or absorbance of the film.
I
j;i 7' 9 i;"r:t Examples 3 and 4 Examples 1 and 2 are repeated using Tinuvin 384, a liquid UV absorber, in place of Tinuvin 328, a solid, with similar results.
Numerous examples of UV-absorbing monomers are known.
For example, polymerizable monomers comprising substituted and unsubstituted benzotriazole derivatives are disclosed in U.S.
s."s Patent Nos. 4,528,311, 4,612,358, 4,868,251, 4,785,063 and 5,112,912. Examples of copolymerizable monomeric UV absorbers Suother than benzotriazole derivatives are, set forth, for example, in U.S. Patent Nos. 3,162,676 and 4,304,895 and in British Patent 885,986.
S one polymerizable terminal double bond, can readily be o:X o incorporated into any of the stabilizing polymers and/or matrix polymers disclosed in the light valve art or in the present invention and will have the effect of appreciably improving the UV resistance of the light valve suspension in which they are incorporated.
One may also attach UV-absorbing groups to either the stabilizing polymer or .the matrix polymer by reacting a UVabsorbing material which comprises a reactable group with a 22 I SSu V oom p ec r i) 4 suitable reactable group in the stabilizing polymer or matrix polymer, so as to bond the UV-absorbing material to the stabilizing or matrix polymer. For example, a stabilizing or matrix polymer may comprise glycidyl acrylate or methacrylate groups. Such groups will react with a UV-absorbing compound such as a benzotriazole derivative that includes a carboxyl group or other reactable group. Such processes, compounds and copolymers are disclosed in U.S. Patent No. 5,112,912.
0 0*[ The amount of the UV absorber will, of course, be :''empirically determined to provide the desired UV absorbance.
0 0 0 Where the UV absorber is in the liquid light valve suspension, a 0 useful amounts may be about 1% by weight or less, usually about 3% or more, based on the weight of the light valve suspension. Where a liquid UV absorber is used, it may provide all of the liquid suspending medium, and this may constitute more than about 70% by weight of the light valve **6 suspension. Where the light modulating element is in the form 0 of a film, the matrix polymer an' the liquid light valve suspension each preferably contains the UV absorber, so that the total amount of the UV absorber is at least oreferably more than about based on the total weight of the light 4 modulating element.
While specific embodiments of the invention have been illustrated, it will be appreciated that the invention is not 23
I,
I
aI90O p@I, IIgfitodoa 21/04/97 limited thereto, since many modifications may be made by one skilled in the art which fall within the true spirit and scope.
of the invention.
ii 0 0 00 *Opi 9.
9494 (I *4 9P04
I
I
Claims (19)
1. A liquid light valve suspension comprising particles suspended in a liquid suspending medium, in which the liquid suspending medium has dissolved therein a UV-absorbing effective amount of a substituted or unsubstituted 2-(2'-hydroxyphenyl)-benzotriazole (hereinafter referred to as benzotriazole derivative).
2. The suspension according to claim 1, wherein the said L-zotriazole derivative is a liquid.
3. The suspension according to claim 1, wherein the S00 said benzotriazole derivative is a solid.
4. A liquid light valve suspension comprising a particles suspended in a liquid suspending medium and a stabilising polymer in said liquid suspending medium to prevent agglomeration of said particles wherein said stabilising polyn.er comprises a UV-absorbing effective amount of the benzotriazole derivative. *0* 9 too The suspension according to claim 4, wherein said stabilising polymer comprises monomeric units thereof copolymerised with monomeric units of the said j benzotriazole derivative.
6. The suspension according to claim 4, wherein the said benzotriazole derivative is bound to said Sstabilising polymer by reaction therewith.
7. The suspension according to claim 5, wherein l said benzotriazole derivative has a group \\MELB01\homeS\Sue\Keep\59381.claims.doc 21/04/97 26 copolymerisable with said monomeric units of said polymeric stabiliser.
8. The suspension according to claim 6, wherein said benzotriazole derivative has a group that can react with said polymeric stabiliser.
9. A film suitable for use as the light modulating element of a light valve, comprising a polymer matrix and droplets of a liquid light valve suspension distributed in the polymer matrix, the polymer matrix or the liquid light valve suspension or both including a UV-absorbing effective amount of a substituted or rr unsubstituted 2-(2'-hydroxyphenyl)-benzotriazole (hereinafter referred to as a benzotriazole derivative). The film according to claim 9, wherein the light valve suspension has the said benzotriazole derivative dissolved therein. :o 11. The film according to claim 9, wherein said light valve suspension comprises a stabilising polymer to prevent agglomeration of said particles, said stabilising polymer comprising a UV-absorbing effective amount of the benzotriazole derivative.
12. The film according to claim 11, wherein said stabilising polymer comprises monomeric units thereof copolymerised with monomeric units of said benzotriazole derivative.
13. The film according to claim 11, wherein said benzotriazole is bound to said stabilising polymer by S\\MELB01\home$\Sue\Keep\59381.claims.doc 21/04/97 l l r l ,a 27 i reaction therewith.
14. The film according to claim 12, wherein said benzotriazole derivative has a group copolymerisable with said monomeric units of said polymeric stabiliser. The film according to claim 15, wherein said benzotriazole derivative has a group that can react with said polymeric stabiliser.
16. The film according to claim 9, wherein said polymer matrix comprises monomeric units thereof copolymerised with monomeric units of said benzotriazole derivative. it *I
17. The film according to claim 9, wherein said benzotriazole derivative is bound to said polymer matrix by reaction therewith.
18. The film according to claim 16, wherein said benzotriazole derivative has a group copolymerisable with said monomeric units of said polymer matrix.
19. The film according to claim 18, wherein said benzotriazole derivative has a group that can react with c said polymer matrix. S 20. A light valve having opposed cell walls, and a light modulating element between said cell walls, wherein the light modulating element is the liquid light valve suspension of any one of claims 1 to 3. S 21. A light valve having opposed cell walls, and a \\MELBO1\home$\sue\Keep\59381.claims.doc 21/04/97 'U 28 4$ 44 I I I I II t II *4 II 4 4 N 9645 I @9 I I 999 5* 9 4 *4 @9 9 9e#* S 0494 @440 4. 4 04 9. light modulating element between said cell walls, wherein the light modulating element is the liquid light valve suspension of any one of claims 4 to 8.
22. A light valve having opposed cell walls, and a light modulating element between said cell walls, wherein the light modulating element is the film of any one of claims 9 to 19.
23. A liquid light valve suspension substantially hereinbefore described in claim 1 with reference to any one of the accompanying examples.
24. A suspension substantially hereinbefore described in claim 8 with reference to any one of the accompanying examples.
25. A light valve substantially hereinbefore described in claim 20 with reference to any one of the accompanying examples. Dated this 23rd day of April 1997 RESEARCH FRONTIERS INCORPORATED By their Patent Attorneys GRIFFITH HACK Fellows Institute of Patent Attorneys of Australia H:\SUeKeep\5938L.c1am.ioc 23/04/97 9> 4~ ,1! it 6 ABSTRACT OF THE DISCLOSURE Light valve suspensions and light valve films are provided with a UV absorber. *44444 4 *9 4 94 4. 9, 4 9 @99 49 94 9 49 44 9 94*0 .494 99 04 9 4400 4409 4 9 9,49 .4 0 94 44 4.449. 9 9
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5990893A | 1993-05-11 | 1993-05-11 | |
| US059908 | 1993-05-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU5938194A AU5938194A (en) | 1994-11-17 |
| AU680231B2 true AU680231B2 (en) | 1997-07-24 |
Family
ID=22026066
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU59381/94A Expired AU680231B2 (en) | 1993-05-11 | 1994-04-12 | Light valve suspensions and films containing UV absorbers and light valves containing the same |
Country Status (2)
| Country | Link |
|---|---|
| AU (1) | AU680231B2 (en) |
| MX (1) | MX9402945A (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4528311A (en) * | 1983-07-11 | 1985-07-09 | Iolab Corporation | Ultraviolet absorbing polymers comprising 2-hydroxy-5-acrylyloxyphenyl-2H-benzotriazoles |
| JPH03255423A (en) * | 1990-01-12 | 1991-11-14 | Takiron Co Ltd | Light control material |
| AU669135B2 (en) * | 1991-11-01 | 1996-05-30 | Research Frontiers Incorporated | Light valve employing a film comprising an encapsulated liquid suspension, and method of making such film |
-
1994
- 1994-04-12 AU AU59381/94A patent/AU680231B2/en not_active Expired
- 1994-04-22 MX MX9402945A patent/MX9402945A/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4528311A (en) * | 1983-07-11 | 1985-07-09 | Iolab Corporation | Ultraviolet absorbing polymers comprising 2-hydroxy-5-acrylyloxyphenyl-2H-benzotriazoles |
| JPH03255423A (en) * | 1990-01-12 | 1991-11-14 | Takiron Co Ltd | Light control material |
| AU669135B2 (en) * | 1991-11-01 | 1996-05-30 | Research Frontiers Incorporated | Light valve employing a film comprising an encapsulated liquid suspension, and method of making such film |
Also Published As
| Publication number | Publication date |
|---|---|
| MX9402945A (en) | 1995-01-31 |
| AU5938194A (en) | 1994-11-17 |
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