|Publication number||US3765896 A|
|Publication date||16 Oct 1973|
|Filing date||22 Nov 1971|
|Priority date||22 Nov 1971|
|Publication number||US 3765896 A, US 3765896A, US-A-3765896, US3765896 A, US3765896A|
|Original Assignee||Eastman Kodak Co|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (3), Referenced by (59), Classifications (10)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent 1 Fox [ Oct. 16, 1973  Assignee: Eastman Kodak Company,
 Filed: Nov. 22, 1971  Appl. No.: 200,830
 US. Cl. 96/89, 96/91 R, 96/115 R, G03c/l/52  Int. Cl G03c 1/72, G03c H68  Field of Search 96/89, 90, 91 R, 96/115 R, 48 R  References Cited UNITED STATES PATENTS 3,600,168 8/1971 Lawton 96/90 X 1/1967 Rauner et a1. 96/89 3/1969 Fox 96/115 R Primary Examiner-Norman G. Torchin Assistant ExaminerWon H. Louie, Jr. Attorney-Robert W.- Hampton et al.
[5 7 ABSTRACT Direct-positive photographic compositions are disclosed, the compositions including a radiationsensitive photobleachant and a colored, stable 2- amino-aryl-l-oxyl-3-oxide-2-imidazoline free radical. When the compositions are exposed to activating radiation for the photobleachant, the colored stable-free radical is bleached or decolorized such that the exposed areas of the composition exhibit lower density and/or different coloring than the unexposed areas. Direct positive images are produced thereby. These compositions can be carried on a support to prepare photographic elements.
8 Claims, No Drawings PHOTOGRAPI-IIC ELEMENT CONTAINING A LIGHT SENSITIVE PHOTOBLEACHANT AND A COLORED STABLE 2-AMINO-ARYL-7-OXYL-3-OXIDE-2- IMIDAZOLINE FREE RADICAL FIELD OF THE INVENTION The present invention relates to photography and particularly to direct-positive photographic compositions and elements including a colored, stable-free radical and a photobleachant.
PRIOR ART General reference to the use of stable-free radicals in single component imaging systems has been made in papers presented by W. R. Bard at SPSE 2nd Symposium on Unconventional Photographic Systems, Washington, D. C. Oct. 21-28, 1967 and at the Society of Plastics Engineers, Mid-hudson Section November, 1967.
The use of stable-free radicals as sensitizers to increase the photoresponsive characteristics of photoconductive insulating compositions and photohardenable polymer compositions is described in U. S. Pat. No. 3,434,833 to Fox issued Mar. 25, 1969.
Negative working direct imaging systems, i.e. those which are based on the formation of increased color or density in exposed areas, which systems relate to combinations of a color generator with a photooxidant are described in, for example, British Pat. No. 1,047,796; U. S. Pat. Nos. 3,359,109; 3,360,370; 3,395,018; 3,44- 5,233; 3,445,234; and Canadian Pat. No. 798,260.
Furthermore, Canadian Pat. No. 822,049 discloses the use of light-sensitive free radicals which upon exposure to actinic radiation react with a color forming compound to produce areas of density in a negative system, and in a positive system a colored compound which is bleached to provide less density in the exposed areas.
Although many of these systems, as already described, make use of photo-imaging systems comprising a photo-active compound and a color producing compound which reacts with the photoactivator upon exposure to light, no systems have been disclosed which uti-.
lize 2-aminoaryl-1-oxyl-3-oxide-2-imidazoline colored stable-free radicals to produde a direct positive and photo-bleachant image. Other patents, describing the use of colored free radicals in combination with photobleachants are U. S. Pat. No. 3,600,168 and its corresponding patent, Canadian Pat. No. 874,372 and British Pat. No. 1,213,823.
A system such as the one described herein overcomes many of the disadvantages exhibited by conventional materials of this type which include relatively high cost, instability of images, generation of offensive odors or poisonous vapors making them difficult to handle, low speed, poor contrast and insufficient resolution. Furthermore, in many known systems, the use of halogenated organic photoactivators which are generally extremely volatile and poisonous is required.
Accordingly, it is an object of this invention to provide novel direct-positive photographic compositions and elements.
Another object of this invention is to provide new direct positive photographic processes.
Still other objects and advantages of the present invention will become apparent from a reading of the following specification and appended claims.
STATEMENT OF THE INVENTION The objects of this invention are accomplished with direct-positive photographic compositions including a radiation-sensitive photobleachant, (i.e., a compound that when exposed to activating rays forms a species that can react with a colored, stable free radical to lower the density or change the color of the free radical) and a colored, stable free radical are provided. They are non-toxic, efficient and produce positive images on exposure. These compositions can be used in conjunction with a support material to prepare photographic elements. The photographic compositions can be coated on a support as a layer or imbibed into a porous support material.
DESCRIPTION OF PREFERRED EMBODIMENT(S) Direct-positive (i.e. producing a positive image directly on exposure) photographic compositions of the present type include a radiation-sensitive photobleachant and a colored, stable free radical having the fora. each of R R, R and R independently represents one of alkyl group, an alkoxy group or an aryl group, and
b. R represents an aminoaryl group having from six to 14 atoms in a monoor polycyclic aromatic nucleus, with the amino moiety having the formula wherein each of R and R independently represents one of an alkyl group or an aryl group (preferably phellnonepreferredembodiment, R and R are alike.
As used herein, the term alkyl group includes straight or branched chain aliphatic groups having from one to eight carbon atoms in the carbon chain used to define the group nomenclature, such as methyl, ethyl, 2- chloroethyl, isopropyl, butyl, pentyl, heptyl, n-octyl,
7-methyloctyl and the like alkyl groups. Lower alkyl groups having one to four carbon atoms are preferred. The term alkoxy group refers to etherified alkyl groups, also designated alkyloxide groups, and include an alkyl moiety such .as those described herein chemically bonded to an oxygen atom, for example, methoxy, ethoxy, propoxy, isobutoxy, pentyloxy, n-octyloxy, etc. Lower alkoxy groups having from one to four carbon atoms are preferred. The term aryl group, as used herein, refers to and includes aromatic groups derived from monoand polycyclic carbocyclic nuclei and having from six to 14 atoms in a monoor polycyclic nucleus, such as phenyl, p-tolyl, naphthyl, anthryl, etc.
Free radical precursors from which free radicals of pared by treatment of the appropriate stable free radical precursor with a suitable oxidation catalyst, for example active lead dioxide in benzene solution, or any other similar oxidation catalyst well known to those the present type can be prepared are themselves able 5 skilled in the art.
to be prepared by the reaction of an ortho bis(hydrox- As mentioned herein, the colored, stable free radical ylamino) alkane with an appropriate arylamino benzalis used in conjunction with a light-activatable photodehyde in an organic solvent. Depending on the particbleachant. When exposed to activating rays, e.g. ultraular substituents represented by R R, R and R, the violet light, other actinic rays visible light or the like, ortho bis(hydroxylamino) alkane can be substituted 10 the photobleachants useful herein are capable of reactwith alkyl, alkoxy or aryl groups. As an example, when ing with the free radical. It is theorized that this capaeach of R R, R and R is a methyl radical, the alkane bility may be the result of the photogeneration of a reis 2,3-bis(hydr0Xy min0).-2, dime ylbu l' active species such as a radical, radical ion, ion or hyprecursors useful in preparing stable free radical pr drogen atom. Amplification factors may be introduced cursors and stable free radicals described herein in- 15 i m instances since t o or mor rea tive species clude such compounds as 2,3-bis(hydroxylamino)-2,3- may b f med u n b or tion of a single photon. dimethoxybutane, etc. Exemplary photobleachants that may be utilized The stable free radicals of the present type are preherein in lude the following:
Number Name Structure 1 4-diethylaminobenzenediazonium tetrafluoborate or hexafluophosphate (CaHrhNQ-Nz BFF or IFu' 2 4-methoxybenzenedlazonium tetrachlorozincate CH O N2*)ZnC14" 2 3 i-phenoxybenzenediazonium tetrachlorozincate CsH50 N2* ZllOlt" 4 1,2-bis-2,4,5-triphenylimidazoles CrHr CrH N:CH5
06255 H CoH5 5 2,2-bis-2,4,5-triphenylimidazole C0115 =N Q =CaH5 i /=N CBHB bI: H C H 6 1,1-bis2,4,5-triphenylimidazole C 13 7 1,2'-bis 2-o-ch1orophenyl4,5-diphenylimidazole N: N:i\
8 2,2-az0bisl2-methylpropionitrile] (CH3)2C(CN)N:NC(CN)(CH:)2
9 Polyethylerleglycol H0CH2CHlO OH 10 Benzophenone (3511 000511 11 Benzophenone with polyethylene glycol.-. l2. Benzophenone with benzhydrol 13...- Tetra-p-tolylhydrazine (p-CHaCaHr)zNN(CuHsC a-Dh 14 Tetraphenylhydrazine (CsH5)2NN(Ca 5)2 l5 N,N'-bicarbazyl TABLE-Continued Number Name Structure 16 N,N-bistetraphenylpyrrole &1. pin. (fuHs 0,115
l C 5 0115 CtHs CBHE 17 Benzoyl peroxide CdHsC O O- 18 Cumene hydroperoxide 0 0H CH3CCH3 19 1,8-pyrenedione 20 1,8-pyrenedione with polyethylene glycol 0 0 Generally, any one or more of the above-described photobleachants may be used in combination with the aforementioned stable-free radicals so that upon exposure to light, a reaction occurs which bleaches the colored free radical and produces a decrease in color density in exposed regions, thereby producing desired direct positive image. Generally, the mole ratio of free tor blade coating, etc. It is desirable that the polymer binder for the free radical and the photobleachant as well as the solvent therefor and the support upon which the coating solution may be applied do not react with either the stable-free radical or the photobleachant. Among the polymeric binders which have been found useful herein are cellulose esters such as for example, cellulose acetate, cellulose acetate butyrate and cellulose acetate propionate; polyester materials, especially poly(ethylene therephthalate), polyvinyl and poly-aolefin resins, all of which may be codissolved with the photoreactants using conventional solvents such asthe alcohols, acetone, methylene chloride, naphtha and a wide variety of other materials. When a binder is used, the concentration of the combined free radical and photo-bleachant generally range from about 1 weight percent to about 90 weight percent, based on the total weight of the composition, with a preferred range occurring from about 2 weight percent to about 60 weight percent. However, the concentration of photo reactants would be 100 percent in the case where a binder is not used and the active components are, for example, imbibed into a porous support.
If a support is utilized to prepare a photographic element. Useful materials include conventional photographic support like glass, metal, paper or the resinous supports, e.g., cellulose acetate, poly(ethylene terephthalate), poly-a-olefms, polystyrenes, etc., which are .well known in the photographic arts, may be used.
Once prepared, the photographic compositions or elements of the present type can be exposed to actuating rays for the photobleachant and image formation occurs directly on exposures. It is theorized that the reaction which occurs upon exposure of the photosensitive compositions of the present invention to activating rays may be described generically and most simply as follows:
KY XY (photoactivated) (photo-bleaehant) (b) R- XY RX Y colored stable-free colorless species radical 2Y' Y-Y (inactive) The following examples are included for a further understanding of the invention.
EXAMPLE I A photographic composition of the present type is prepared by dissolving 0.03 g. of l-oxyl-2-[4-dimethylamino phenyl]-4,4,5,5-tetramethyldehydroimidazole- 3-oxide and I .131 g. of 4- diethylaminobenzenediazonium tetra-fluoroborate along with 10 g. of cellulose acetate butyrate, in 25 mls. of 2-methoxyethanol plus mls. of methylene chloride. The coating solution is coated on a paper support at a wet thickness of 0.005 inches. When dry, a portion of the photographic element is imagewise exposed to ultraviolet rays in the exposure in a Filmsort 086 unit of a diazo printer which contains a mercury arc source. The coating bleached to nearly colorless in the exposed area, while it remains unchanged in unexposed areas. Color change is from blue to colorless in exposed areas. A control coating is prepared in the same manner, except that the diazonium salt photobleachant is omitted. This coating is then exposed in the same manner, in a Filmsort 086 Diazo printer. After a period of 10 minutes, the element is removed, and shows no visible signs of bleaching in the exposed areas. No differential density between the exposed and unexposed areas can be detected thereby indicating that the free-radical exhibits high stability.
EXAMPLE II The procedure described in Example I is used except that the diazonium salt component is replaced by 0.5 g. of polyethylene glycol, average MW 600. This coating is also bleached in the exposed areas from blue to colorless, but remains unchanged in unexposed areas.
EXAMPLE Ill The procedure described in Example I is used to prepare another photographic element, except the diazonium salt is replaced by 0.04 g. of benzophenone, and
0.04 g. of benzhydrol were used; and also 2 g. of cellulose acetate butyrate in 5 mls. of Z-methoxyethanol plus mls. of methylene chloride is used. The resultant elementbleaches in exposed areas but remains unchanged in unexposed area. Color change is from blue to colorless.
it will be appreciated that the convenient procedures described herein, such as in the Examples, can be used with any stable free radicals and photo-bleachants of the present type. Such variations will be apparent to those skilled in the art.
Other ingredients such as sensitizers, matting agents, plasticizers, etc. may also be added to the imaging systems of the present invention to improve various aspects and characteristics thereof. Fixing and/or stabilization treatments may be used to improve the quality and/or stability of the images formed using the. imaging products of the present invention.
For example, in some instances, e.g., when a bis- 2,4,5-triarylimidazole is used as the photobleachant, it
may be desirable to obtain a degree of fixation such as might be required for use of the image in the presence of ultraviolet light. This can be accomplished by preferentially eliminating the photo-bleachant, e.g., bis-2,4,5- triarylimidazole, from the unexposed areas through the use of solvent washout of the photobleachant or a redox system such as the quinone-polyethylene oxide system which is activated at wavelengths different than the photo-bleachant and on activation deactivates the photobleachant. When a diazonium salt is used as the photobleachant, it may be removed from the nonimage areas by incorporating a conventional diazo cou pler, for example 2-hydroxynaphthol in the system and coupling the diazonium salt by exposure of the system to a basic medium without generating extensive density in the non-image area. I
There has thus been described herein a series of imaging elements which find advantageous use in applications wherein photosensitive elements which react only to, for example, light of short wavelength, e.g., specific wavelengths of ultraviolet light, but have low sensitivity to light of longer wavelengths, e.g., visible light, so that the resulting image is substantially stable under normal conditions of use and does not require additional fixation or stabilization treatments.
The invention has been described in detail with specific reference to preferred embodiments thereof, however, it will be readily recognized that variations and modifications can be made within the spirit and scope of the invention and the same should not be limited except as defined in the appended claims.
There is claimed: 1. A direct-positive photographic composition comprising a radiation-sensitive photobleachant selected from the group consisting of 4-dialkylaminobenzene diazoniurn salts, 4-alkoxybenzenediazonium salts, 4- aryloxybenzenediazonium salts, bis-2,4,5- triphenylirnidazoles, azobispropionitriles, poly- (ethylene glycols), benzophenones, tetraphenyl pyrroles, benzo-peroxides, cumene hydroperoxides, 1,8- pyrenediones and mixtures thereof and a colored, stable free radical having the formula:
R and R each representing independently one of an alkyl group or an aryl group as described above.
2. A direct-positive photographic composition as described in claim 1 wherein, in the free radical, each of R, R, R and R is a lower alkyl group and each of R and R are alike and are either a methyl group, and ethyl group or a phenyl group.
3. A direct-positive photographic composition as described in claim 1 wherein said free radical and said photobleachant are included in a molar ratio of from 1:1 to about 1:10.
4. A direct-positive photographic composition as described in claim 1 and further comprising a filmforming polymeric binder.
5. A direct-positive photographic composition as described in claim 4 wherein said binder is cellulose acetate, cellulose acetate butyrate, cellulose acetate propionate or gelatin.
6. A photographic element comprising a support having thereon a direct-positive photographic composition as described in claim 1.
7. A photographic element comprising a support having thereon a direct-positive photographic composition as described in claim I.
8. A photographic element as described in claim 6- wherein said support comprises a porous material and said direct-positive photographic composition is imbibed into the pores of said support.
a w w 4- m
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3300314 *||1 Feb 1963||24 Jan 1967||Eastman Kodak Co||Nonsilver, light-sensitive photographic elements|
|US3434833 *||26 Jul 1965||25 Mar 1969||Eastman Kodak Co||Stable free radicals as activators for photoconductive and photohardenable polymer light-sensitive systems|
|US3600168 *||15 Nov 1966||17 Aug 1971||Bard Lab Inc||Light sensitive reproduction sheet and method and coating composition therefor using free radicals|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4863827 *||20 Oct 1986||5 Sep 1989||American Hoechst Corporation||Postive working multi-level photoresist|
|US5616443||1 Jun 1995||1 Apr 1997||Kimberly-Clark Corporation||Substrate having a mutable colored composition thereon|
|US5643356||5 Jun 1995||1 Jul 1997||Kimberly-Clark Corporation||Ink for ink jet printers|
|US5643701||1 Jun 1995||1 Jul 1997||Kimberly-Clark Corporation||Electrophotgraphic process utilizing mutable colored composition|
|US5645964||5 Jun 1995||8 Jul 1997||Kimberly-Clark Corporation||Digital information recording media and method of using same|
|US5681380||19 Dec 1996||28 Oct 1997||Kimberly-Clark Worldwide, Inc.||Ink for ink jet printers|
|US5683843||22 Feb 1995||4 Nov 1997||Kimberly-Clark Corporation||Solid colored composition mutable by ultraviolet radiation|
|US5685754 *||19 May 1995||11 Nov 1997||Kimberly-Clark Corporation||Method of generating a reactive species and polymer coating applications therefor|
|US5686503 *||22 Jan 1996||11 Nov 1997||Kimberly-Clark Corporation||Method of generating a reactive species and applications therefor|
|US5700850||5 Jun 1995||23 Dec 1997||Kimberly-Clark Worldwide||Colorant compositions and colorant stabilizers|
|US5709955||16 Oct 1996||20 Jan 1998||Kimberly-Clark Corporation||Adhesive composition curable upon exposure to radiation and applications therefor|
|US5721287||5 Jun 1995||24 Feb 1998||Kimberly-Clark Worldwide, Inc.||Method of mutating a colorant by irradiation|
|US5733693||2 Jan 1997||31 Mar 1998||Kimberly-Clark Worldwide, Inc.||Method for improving the readability of data processing forms|
|US5739175||5 Jun 1995||14 Apr 1998||Kimberly-Clark Worldwide, Inc.||Photoreactor composition containing an arylketoalkene wavelength-specific sensitizer|
|US5747550||5 Jun 1995||5 May 1998||Kimberly-Clark Worldwide, Inc.||Method of generating a reactive species and polymerizing an unsaturated polymerizable material|
|US5773182||5 Jun 1995||30 Jun 1998||Kimberly-Clark Worldwide, Inc.||Method of light stabilizing a colorant|
|US5782963||27 Nov 1996||21 Jul 1998||Kimberly-Clark Worldwide, Inc.||Colorant stabilizers|
|US5786132||29 May 1996||28 Jul 1998||Kimberly-Clark Corporation||Pre-dyes, mutable dye compositions, and methods of developing a color|
|US5798015||5 Jun 1995||25 Aug 1998||Kimberly-Clark Worldwide, Inc.||Method of laminating a structure with adhesive containing a photoreactor composition|
|US5811199||5 Jun 1995||22 Sep 1998||Kimberly-Clark Worldwide, Inc.||Adhesive compositions containing a photoreactor composition|
|US5837429||5 Jun 1996||17 Nov 1998||Kimberly-Clark Worldwide||Pre-dyes, pre-dye compositions, and methods of developing a color|
|US5849411||5 Jun 1995||15 Dec 1998||Kimberly-Clark Worldwide, Inc.||Polymer film, nonwoven web and fibers containing a photoreactor composition|
|US5855655||15 Apr 1997||5 Jan 1999||Kimberly-Clark Worldwide, Inc.||Colorant stabilizers|
|US5858586||16 May 1997||12 Jan 1999||Kimberly-Clark Corporation||Digital information recording media and method of using same|
|US5865471||21 Dec 1994||2 Feb 1999||Kimberly-Clark Worldwide, Inc.||Photo-erasable data processing forms|
|US5885337||31 Oct 1997||23 Mar 1999||Nohr; Ronald Sinclair||Colorant stabilizers|
|US5891229||31 Jul 1997||6 Apr 1999||Kimberly-Clark Worldwide, Inc.||Colorant stabilizers|
|US5908495||24 Sep 1997||1 Jun 1999||Nohr; Ronald Sinclair||Ink for ink jet printers|
|US6008268||22 Jan 1998||28 Dec 1999||Kimberly-Clark Worldwide, Inc.||Photoreactor composition, method of generating a reactive species, and applications therefor|
|US6017471||23 Apr 1997||25 Jan 2000||Kimberly-Clark Worldwide, Inc.||Colorants and colorant modifiers|
|US6017661||8 Oct 1997||25 Jan 2000||Kimberly-Clark Corporation||Temporary marking using photoerasable colorants|
|US6033465||5 Apr 1996||7 Mar 2000||Kimberly-Clark Worldwide, Inc.||Colorants and colorant modifiers|
|US6054256||3 Dec 1998||25 Apr 2000||Kimberly-Clark Worldwide, Inc.||Method and apparatus for indicating ultraviolet light exposure|
|US6060200||3 Feb 1998||9 May 2000||Kimberly-Clark Worldwide, Inc.||Photo-erasable data processing forms and methods|
|US6060223||3 Dec 1998||9 May 2000||Kimberly-Clark Worldwide, Inc.||Plastic article for colored printing and method for printing on a colored plastic article|
|US6063551||16 Nov 1998||16 May 2000||Kimberly-Clark Worldwide, Inc.||Mutable dye composition and method of developing a color|
|US6066439||3 Dec 1998||23 May 2000||Kimberly-Clark Worldwide, Inc.||Instrument for photoerasable marking|
|US6071979||26 Dec 1997||6 Jun 2000||Kimberly-Clark Worldwide, Inc.||Photoreactor composition method of generating a reactive species and applications therefor|
|US6090236||31 Dec 1997||18 Jul 2000||Kimberly-Clark Worldwide, Inc.||Photocuring, articles made by photocuring, and compositions for use in photocuring|
|US6099628||23 Jan 1997||8 Aug 2000||Kimberly-Clark Worldwide, Inc.||Colorant stabilizers|
|US6120949||3 Dec 1998||19 Sep 2000||Kimberly-Clark Worldwide, Inc.||Photoerasable paint and method for using photoerasable paint|
|US6127073||3 Dec 1998||3 Oct 2000||Kimberly-Clark Worldwide, Inc.||Method for concealing information and document for securely communicating concealed information|
|US6168654||6 Apr 1999||2 Jan 2001||Kimberly-Clark Worldwide, Inc.||Colorant stabilizers|
|US6168655||15 Dec 1998||2 Jan 2001||Kimberly-Clark Worldwide, Inc.||Colorant stabilizers|
|US6211383||10 Feb 1998||3 Apr 2001||Kimberly-Clark Worldwide, Inc.||Nohr-McDonald elimination reaction|
|US6228157||20 Jul 1999||8 May 2001||Ronald S. Nohr||Ink jet ink compositions|
|US6235095||1 Jun 1999||22 May 2001||Ronald Sinclair Nohr||Ink for inkjet printers|
|US6242057||29 Apr 1998||5 Jun 2001||Kimberly-Clark Worldwide, Inc.||Photoreactor composition and applications therefor|
|US6265458||28 Sep 1999||24 Jul 2001||Kimberly-Clark Worldwide, Inc.||Photoinitiators and applications therefor|
|US6277897||3 Jun 1999||21 Aug 2001||Kimberly-Clark Worldwide, Inc.||Photoinitiators and applications therefor|
|US6294698||16 Apr 1999||25 Sep 2001||Kimberly-Clark Worldwide, Inc.||Photoinitiators and applications therefor|
|US6331056||24 Feb 2000||18 Dec 2001||Kimberly-Clark Worldwide, Inc.||Printing apparatus and applications therefor|
|US6342305||28 Dec 1999||29 Jan 2002||Kimberly-Clark Corporation||Colorants and colorant modifiers|
|US6368395||12 May 2000||9 Apr 2002||Kimberly-Clark Worldwide, Inc.||Subphthalocyanine colorants, ink compositions, and method of making the same|
|US6368396||19 Jan 2000||9 Apr 2002||Kimberly-Clark Worldwide, Inc.||Colorants, colorant stabilizers, ink compositions, and improved methods of making the same|
|US6486227||19 Jun 2001||26 Nov 2002||Kimberly-Clark Worldwide, Inc.||Zinc-complex photoinitiators and applications therefor|
|US6503559||3 Jun 1999||7 Jan 2003||Kimberly-Clark Worldwide, Inc.||Neonanoplasts and microemulsion technology for inks and ink jet printing|
|US6524379||12 Jan 2001||25 Feb 2003||Kimberly-Clark Worldwide, Inc.||Colorants, colorant stabilizers, ink compositions, and improved methods of making the same|
|EP0065326A1 *||26 Apr 1982||24 Nov 1982||AGFA-GEVAERT naamloze vennootschap||A photosensitive recording material and photographic processes wherein said material is used|
|U.S. Classification||430/171, 430/374, 430/334, 430/339|
|International Classification||G03C1/73, G03C7/02|
|Cooperative Classification||G03C1/73, G03C7/02|
|European Classification||G03C7/02, G03C1/73|