US3464841A - Method of preparing security paper containing an ultraviolet inhibitor - Google Patents

Method of preparing security paper containing an ultraviolet inhibitor Download PDF

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US3464841A
US3464841A US3464841DA US3464841A US 3464841 A US3464841 A US 3464841A US 3464841D A US3464841D A US 3464841DA US 3464841 A US3464841 A US 3464841A
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paper
security
mark
impression
method
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Bruce D Skofronick
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Customark Corp
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Customark Corp
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    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/40Agents facilitating proof of genuineness or preventing fraudulent alteration, e.g. for security paper
    • D21H21/44Latent security elements, i.e. detectable or becoming apparent only by use of special verification or tampering devices or methods
    • D21H21/46Elements suited for chemical verification or impeding chemical tampering, e.g. by use of eradicators

Description

United States Patent 3,464,841 METHOD OF PREPARING SECURITY PAPER CONTAINING AN ULTRAVIOLET INHIBITOR Bruce D. Skofronick, Appleton, Wis., assiguor, by mesne assignments, to Customark Corporation, Appleton, Wis., a corporation of Wisconsin No Drawing. Filed Oct. 23, 1965, Ser. No. 504,115 Int. Cl. B41m 3/14 U.S. Cl. 117-1 2 Claims ABSTRACT OF THE DISCLOSURE A paper product with a security impression and the method of preparation therefor. A selected area of the paper is treated with a liquid composition having an inhibitor chemical comprising an ultraviolet absorbing organic chemical in an amount so that the treated area is invisible in the dry state and visually detectable after wetting the paper.

This invention relates to a paper product with an incorporated security impression, and to a method of making such a paper product.

There have been many attempts and many proposed Ways in the art to check the authenticity of various paper, ofiicial or otherwise. A particular effort has been concerned with applying impressions which are normally invisible, but which are rendered visible by appropriate manipulative steps. Such an approach has many advantages because it can be applied to many different types of papers, irrespective of the number of conventionally printed visible ink or other impressions applied to the paper. Various types of paper pro-ducts are desirably adated for such a security impression mark, such as passports, bonds, official government or private stationery, industrial or artistic drawings, and any type of paper having some meaningful or commercially important visible impression on the surface thereof.

It is a primary object of the present invention to provide a paper product and a method by which a security impression is simply and conveniently applied to paper so that it is invisible in the dry state, and may be rendered visible for checking authenticity or otherwise by the quick, economical and simple provision of wetting the paper.

Another object is a security paper product and method whereby any selected security impression can be applied to any portion of a hard, finished paper surface, and be retained therein to check the authenticity of the paper one or more times.

Another object is the security paper product and method by which the security impression is conveniently and quickly applied to the surface of finished paper in a liquid state, and said paper is put into use after the security impression is converted into a dry state, without visible perception by uninformed handlers; yet is quickly rendered visible for checking purposes by simply wetting the portion of the paper having the security impression.

Another object is the security paper product and method which permits the paper product to be checked for authenticity or the like on repeated occasions because the security impression is retained over an extended period of time, and is capable of undergoing repeated manipulative steps which render the mark visible for security purposes.

Another purpose is a paper product and method on which a security mark can be applied with any selected configuration or design to identify the paper product, to code the paper product, or otherwise provide a meaningful indication, said mark being normally invisible but capable of being rendered visible quickly, simply and cheaply.

Another object is a method whereby few manipulativc steps and materials are employed to make a finished paper product with the security mark of such a type that the security mark can be checked for authenticity or other information relative to the paper product.

Such objects are realized, as well as other objects which will become apparent by considering the following disclosure, which teaches representative ways of preparing and using security paper products.

The invention provides that a security impression mark is normally invisible on a surface sheet of paper or in the matrix of the paper but is rendered visible by a very quick and economical manipulation which can be instantly and universally practiced, namely, wetting the paper with water. In the wet state, the previously invisible security mark is rendered visible, and again becomes invisible in the dry state. It is a marked advantage of the invention that such security marks can be repeatedly made visible over extended periods of time by rewetting the paper. There is a further advantage that such security impression mark is ink receptive, by which is meant that it receives printed or other ink impressions without blurring, feathering, skipping or the like. In other words, the security impression can receive normally visible written, drawn or printed impressions. Such visible impressions include the non-ink type, such as pencil, crayola and the like.

The security impression mark or configuration or design is laid down or applied to a portion of the surface of finished paper. The security impression mark is laid down from a liquid composition which contains one or more ultraviolet absorbent organic chemicals and an organic solvent which is removed after application by evaporation, heat or the like. In a sense, the security impression may be said to be printed where a stamp, die or the like is used to impart the design or configuration onto the hard finished surface. The liquid composition may be spread as a film on such impression transferring means and applied with momentary pressure. It will be appreciated, however, that other means may be used for applying the security impression to the surface of the paper, such as manual inscription with a brush or the like. It will be seen that in certain operations a simple hand stamp may be used to put the invisible security impression or mark on occasional papers which are presented to certain agencies such as those which handle secret reports, passports or the like. It will likewise be seen that such security impressions could be continuously impressed on papers in large scale operations by employing a printing roll or printing plate or a stencil operation, or similar means for large scale operations.

The ultraviolet absorbing organic chemicals which are useful in the invention are generally known in the art and represent various benzophenone types, particularly hydroxy and al-koxy types of substituted benzophenones, among which are 2-hydroxy-4-methoxybenzophenone supplied as Uvinul M-40; ethyl-2-cyano-3,2 diphenyl acrylate supplied as Uvinul N-35; 2-hydroxy-4-methoxybenzophenone-S-sulfonic acid supplied as Uvinul MS-40; and 2,4-dihydroxybenzophenone supplied as Uvinul 400. All of the foregoing Uvinul ultraviolet absorbent organic chemicals are made and sold by Antara Chemical Company. Other available and useful ultraviolet absorbing organic chemicals are the series supplied under the designation of Eastman Inhibitors by the Eastman Chemical Company. They are:

HPT-Hexamethylphosphoric triamide DHPB-2,4-dihydroxybenzophenone OPSp-Octylphenyl salicylate RMB-Resorcinal monobenzoate DOBP-4-dodecyloxy-2-hydroxybenzophenone 7 Other ultraviolet absorbing chemicals commercially available on the market are:

Cyasorb UV92, Hydroxy-4-methoxybenzophene Agent AT539 (Univul N 539)2 ethyl heXyl-Z- cyano-3,3 diphenyl acrylate.

The Eastman inhibitor HPT is supplied as a liquid containing organic solvent, and may be applied in such a form directly to the surface of the finished paper and dried. The OPS and RMB have ester linkages but are believed to convert to hydroxybenzophenones under the influence of ultraviolet rays. Other ultraviolet absorbent chemicals are provided in dry powder form and are converted to a liquid composition by dissolving the powder in an organic solvent. The concentration of the ultraviolet organic chemical absorbing agent in the organic solvent can be varied within selected ranges, depending on the consistency of the composition which the practitioner desires to handle, and the manner of applying the liquid composition to the surface paper. It will be appreciated that the concentration should not be too great because then the workability of the liquid composition is impaired; likewise, it may become more difiicult for the ultraviolet absorbing chemical to adhere to the finished paper. On the other hand, the concentration should be present in sufiicient amounts so that a visually detectable mark appears after wetting the paper. Understandably, if the concentration is too low, an unsatisfactory type of mark may be laid down in that it has gaps or breaks or streaks in the particular design selected. Such workable concentration can be readily determined without difiiculty by those skilled in the art. In general,

sorbing chemical. They may include the various glycol ethers, such as ethylene glycol monomethyl ethers and the corresponding dimethyl ethers, monoethyl ethers, diethyl ethers, monobutyl ethers, monohexyl ethers, and the like.

The diethylene glycols are also useful, such as diethylene glycol monomethyl ether, and the corresponding monoethyl ethers, monobutyl ethers and diethyl ethers. Other solvents which are useful are dimethyl for mamide, triacetin, N-butyl acetate, monoethyl ether acetate, cyclohexanone and the like. The solvent selected has only a few requirements to meet operability, namely, its ability to dissolve the ultraviolet absorbing organic chemical, its volatility so as to allow convenient removal after application by evaporation, heat, passage of warm air or the like, and its compatibility with the paper. By compatibility is meant that the organic solvent does not adversely affect the paper by discoloring it or leaving other telltale signs after removal following application. Likewise, the organic solvent should not damage the paper by any substantial weakening of the fibers, caustic action or the like.

In the following table, a representative number of examples are summarized wherein various ultraviolet absorbing chemicals in a liquid composition are applied to the surfaces of finished papers. The organic solvent liquid composition is methyl Carbitol (diethyleneglycol methyl ether) and the ultraviolet absorbing organic chemicals are present therein, in a concentration of about 10% by weight. Such a liquid composition is contacted with an elastomeric hand stamp, and the wetted hand stamp is then contacted with a portion of the surface of the finished paper. The security impression is allowed to dry by evaporation of the organic solvent. All of the security impressions in the dry state were invisible, or virtually invisible, and were distinctly visible after wetting the paper with water. The results of artificially aging the papers with the security impression marks are summarized.

Material tested Eastman Inhibitor HPI Eastman Inhibitor D H13 P Eastman Inhibitor 0 PS TABLE I Security marks visibility Ink Fadeometer Oven age feathering a 10% concentration of the organic chemical and organic solvent will provide an operable liquid composition which leads to satisfactory security impression marks. This concentration can be raised to about 20% or 30%, depending on the degree of solubility of the chemical in a particular solvent, and the viscosity of the resulting liquid composition, which may affect handling, as previously discussed. In general, concentrations substantially below 5% will not lead to the good results obtained with higher concentrations. It has been found that a large variety of these ultraviolet absorbent organic chemicals may be used to make the security impressions, so long as the chemical is compatible with the paper for the intended purpose, that is, it dries to an invisible or virtually invisible mark and does not discolor or provide any substantial telltale signs in the dry state. Likewise, the chemical must be compatible in the sense that it is ink-receptive and preferably useful over extended periods of time so that it can be subjected to repeated steps of exposure upon wetting, disappearance upon drying, and re-exposure upon rewetting.

A large variety of organic solvents can be used to prepare the liquid composition with the ultraviolet ab- The indications under the Fadeometer heading report the appearance of the re-wetted mark after six hours in the Fadeometer. The Fadeometer is a well-known instrument for comparing the fading properties of different materials, which are exposed under standard conditions of humidity and the like to a carbon are which operates as artificial sunlight. The designations under the column entitled Oven Age report the appearance of the mark after the paper has been re-wetted following 72 hours in an oven at C. The ink feathering column indicates that the mark has excellent ink receptivity in that none of the ink feathers or blurs on the portion of the paper where the security impression has been applied.

The following Table II indicates various concentrations of the ultraviolet absorbing chemicals which were used to make security impressions by applying a liquid composition containing the material in the stated amount dissolved in methyl Carbitol solvent. The security impression mark formed was satisfactory in that it was invisible or virtually invisible to the casual observer in the dry state, and was visually detectable after wetting the paper with water.

TABLE II Percent b weight of material in methyl Ultraviolet Carbitol material solvent DHBP 6 OF S 22 RMB 6 M-40 22 N-35 22 MS-40 22 400 6 UV-Q 22 In the practice of this invention, the security impression mark can be applied to the surface of the finished paper product or sheet before the conventional visual impressions are applied, or after such conventional visual impressions are applied. The conventional visual impressions referred to include handwriting by pencil, ink or the like; and printing with various printing inks known in the art. This security impression mark can be applied to a portion of the paper surface spaced away from the conventional impression marks, or can be applied to an area of the paper where the conventional impressions have been or will be applied.

If the conventional impressions are of the permanent type then, of course, the paper can be repeatedly wetted and dried to check the paper for reappearance of the security mark. This will check its authenticity, its source, or whatever information the appearance of the security impression or mark will convey to the user. If the conventional visual impressions are smeared, blurred or otherwise defaced by water, it will clearly not ordinarily be reusable, but the reappearance of the security pressure mark in a wetted state will still have served a useful purpose.

The security impression mark can be applied in any one of many selected designs or configurations. Such will be meaningful in the sense that they will authenticate or check out the paper product. It will be appreciated that particularly fanciful or distinctive security impressions may be preferred to customize certain papers, or to code them, or to enumerate them in a series or program. All such advantages may be realized in the practice of the present invention.

I claim:

1. A method for preparing a security paper product With security impressions which includes the steps of:

applying to the surface of a finished sheet of paper a liquid security composition to form a non-continuous impregnation of the sheet, said composition including an ultraviolet inhibitor comprising an ultraviolet absorbing organic chemical selected from the group consisting of 2 hydroxy 4 methoxybenzophenone; ethyl 2 cyano 3, 2 diphenyl acrylate; 2 hydroxy 4 methoxybenzophenone-S-sulfonic acid; 2,4 dihydroxybenzophenone; 2 ethyl hexyl- 2 cyano 3, 3 diphenyl acrylate; hexamethylphosphoric trianide; resorcinol monobenzoate; 4-dodecyloxy 2 hydroxybenzophenone; and p octylphenyl salicylate and an organic chemical solvent, said ultraviolet absorbing organic chemical applied in an amount to be invisible upon subsequent removal of the solvent and visually detectable upon wetting the paper With Water, and

removing the organic solvent to obtain a dry security impression.

2. A method as in claim 1 further characterized by and including the step of initially applying normally visible impressions to the surface of the paper Which serve a desirable meaningful purpose, and then applying the security composition to a selected portion of the paper.

References Cited UNITED STATES PATENTS 3,160,665 12/1964 Siegrist et al. 260591 2,255,696 9/1941 Clifford 117-1 X 3,162,642 12/1964 McCafferty 1171 X OTHER REFERENCES Meyer et al., Abstract 763,146 Cellulose Organic Acid Ester Compositions Containing a 2,5-dialkyl ether of an Aryl Phenone, Aug. 1, 1960.

S. LEON BASHORE, Primary Examiner T. G. FERRIS, Assistant Examiner US. Cl. X.R. 162-140, 158

US3464841A 1965-10-23 1965-10-23 Method of preparing security paper containing an ultraviolet inhibitor Expired - Lifetime US3464841A (en)

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Cited By (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5264081A (en) * 1989-06-01 1993-11-23 Societe Anonyme: Aussedat-Rey Forgery-proof safety paper
US5681380A (en) 1995-06-05 1997-10-28 Kimberly-Clark Worldwide, Inc. Ink for ink jet printers
US5700850A (en) * 1993-08-05 1997-12-23 Kimberly-Clark Worldwide Colorant compositions and colorant stabilizers
US5709955A (en) 1994-06-30 1998-01-20 Kimberly-Clark Corporation Adhesive composition curable upon exposure to radiation and applications therefor
US5721287A (en) 1993-08-05 1998-02-24 Kimberly-Clark Worldwide, Inc. Method of mutating a colorant by irradiation
US5733693A (en) 1993-08-05 1998-03-31 Kimberly-Clark Worldwide, Inc. Method for improving the readability of data processing forms
US5773182A (en) 1993-08-05 1998-06-30 Kimberly-Clark Worldwide, Inc. Method of light stabilizing a colorant
US5782963A (en) 1996-03-29 1998-07-21 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5786132A (en) 1995-06-05 1998-07-28 Kimberly-Clark Corporation Pre-dyes, mutable dye compositions, and methods of developing a color
US5837429A (en) 1995-06-05 1998-11-17 Kimberly-Clark Worldwide Pre-dyes, pre-dye compositions, and methods of developing a color
US5855655A (en) 1996-03-29 1999-01-05 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5858586A (en) 1993-08-05 1999-01-12 Kimberly-Clark Corporation Digital information recording media and method of using same
US5865471A (en) 1993-08-05 1999-02-02 Kimberly-Clark Worldwide, Inc. Photo-erasable data processing forms
US5885337A (en) 1995-11-28 1999-03-23 Nohr; Ronald Sinclair Colorant stabilizers
US5891229A (en) 1996-03-29 1999-04-06 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US6008268A (en) 1994-10-21 1999-12-28 Kimberly-Clark Worldwide, Inc. Photoreactor composition, method of generating a reactive species, and applications therefor
US6017661A (en) 1994-11-09 2000-01-25 Kimberly-Clark Corporation Temporary marking using photoerasable colorants
US6017471A (en) 1993-08-05 2000-01-25 Kimberly-Clark Worldwide, Inc. Colorants and colorant modifiers
US6033465A (en) 1995-06-28 2000-03-07 Kimberly-Clark Worldwide, Inc. Colorants and colorant modifiers
US6071979A (en) 1994-06-30 2000-06-06 Kimberly-Clark Worldwide, Inc. Photoreactor composition method of generating a reactive species and applications therefor
US6099628A (en) 1996-03-29 2000-08-08 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
WO2001005603A1 (en) * 1999-07-16 2001-01-25 Jury Viktorovich Zhvakoljuk Method for protecting information carriers against counterfeiting
US6211383B1 (en) 1993-08-05 2001-04-03 Kimberly-Clark Worldwide, Inc. Nohr-McDonald elimination reaction
US6214766B1 (en) 1999-02-03 2001-04-10 Westvaco Corporation Security feature for paper products
US6228157B1 (en) 1998-07-20 2001-05-08 Ronald S. Nohr Ink jet ink compositions
US6242057B1 (en) 1994-06-30 2001-06-05 Kimberly-Clark Worldwide, Inc. Photoreactor composition and applications therefor
US6265458B1 (en) 1998-09-28 2001-07-24 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6277897B1 (en) 1998-06-03 2001-08-21 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6294698B1 (en) 1999-04-16 2001-09-25 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6331056B1 (en) 1999-02-25 2001-12-18 Kimberly-Clark Worldwide, Inc. Printing apparatus and applications therefor
US6368396B1 (en) 1999-01-19 2002-04-09 Kimberly-Clark Worldwide, Inc. Colorants, colorant stabilizers, ink compositions, and improved methods of making the same
US6368395B1 (en) 1999-05-24 2002-04-09 Kimberly-Clark Worldwide, Inc. Subphthalocyanine colorants, ink compositions, and method of making the same
US6503559B1 (en) 1998-06-03 2003-01-07 Kimberly-Clark Worldwide, Inc. Neonanoplasts and microemulsion technology for inks and ink jet printing
US6524379B2 (en) 1997-08-15 2003-02-25 Kimberly-Clark Worldwide, Inc. Colorants, colorant stabilizers, ink compositions, and improved methods of making the same
US8240410B2 (en) 1999-09-15 2012-08-14 Hill-Rom Services, Inc. Patient support apparatus with powered wheel
US8267206B2 (en) 2000-05-11 2012-09-18 Hill-Rom Services, Inc. Motorized traction device for a patient support

Citations (3)

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Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2255696A (en) * 1938-04-05 1941-09-09 Waterlow & Sons Ltd Means for safeguarding bank notes, bonds, and like documents of value from fraudulent imitation
US3160665A (en) * 1957-03-06 1964-12-08 Ciba Ltd Hydroxy-benzophenones
US3162642A (en) * 1960-07-15 1964-12-22 Nat Marking Mach Co Fluorescent pigments

Cited By (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5264081A (en) * 1989-06-01 1993-11-23 Societe Anonyme: Aussedat-Rey Forgery-proof safety paper
US6211383B1 (en) 1993-08-05 2001-04-03 Kimberly-Clark Worldwide, Inc. Nohr-McDonald elimination reaction
US5700850A (en) * 1993-08-05 1997-12-23 Kimberly-Clark Worldwide Colorant compositions and colorant stabilizers
US6066439A (en) 1993-08-05 2000-05-23 Kimberly-Clark Worldwide, Inc. Instrument for photoerasable marking
US5721287A (en) 1993-08-05 1998-02-24 Kimberly-Clark Worldwide, Inc. Method of mutating a colorant by irradiation
US5733693A (en) 1993-08-05 1998-03-31 Kimberly-Clark Worldwide, Inc. Method for improving the readability of data processing forms
US5773182A (en) 1993-08-05 1998-06-30 Kimberly-Clark Worldwide, Inc. Method of light stabilizing a colorant
US6060200A (en) 1993-08-05 2000-05-09 Kimberly-Clark Worldwide, Inc. Photo-erasable data processing forms and methods
US6060223A (en) 1993-08-05 2000-05-09 Kimberly-Clark Worldwide, Inc. Plastic article for colored printing and method for printing on a colored plastic article
US6054256A (en) 1993-08-05 2000-04-25 Kimberly-Clark Worldwide, Inc. Method and apparatus for indicating ultraviolet light exposure
US6017471A (en) 1993-08-05 2000-01-25 Kimberly-Clark Worldwide, Inc. Colorants and colorant modifiers
US5858586A (en) 1993-08-05 1999-01-12 Kimberly-Clark Corporation Digital information recording media and method of using same
US5865471A (en) 1993-08-05 1999-02-02 Kimberly-Clark Worldwide, Inc. Photo-erasable data processing forms
US5908495A (en) 1993-08-05 1999-06-01 Nohr; Ronald Sinclair Ink for ink jet printers
US6120949A (en) 1993-08-05 2000-09-19 Kimberly-Clark Worldwide, Inc. Photoerasable paint and method for using photoerasable paint
US6127073A (en) 1993-08-05 2000-10-03 Kimberly-Clark Worldwide, Inc. Method for concealing information and document for securely communicating concealed information
US6342305B1 (en) 1993-09-10 2002-01-29 Kimberly-Clark Corporation Colorants and colorant modifiers
US6242057B1 (en) 1994-06-30 2001-06-05 Kimberly-Clark Worldwide, Inc. Photoreactor composition and applications therefor
US6071979A (en) 1994-06-30 2000-06-06 Kimberly-Clark Worldwide, Inc. Photoreactor composition method of generating a reactive species and applications therefor
US6090236A (en) 1994-06-30 2000-07-18 Kimberly-Clark Worldwide, Inc. Photocuring, articles made by photocuring, and compositions for use in photocuring
US5709955A (en) 1994-06-30 1998-01-20 Kimberly-Clark Corporation Adhesive composition curable upon exposure to radiation and applications therefor
US6008268A (en) 1994-10-21 1999-12-28 Kimberly-Clark Worldwide, Inc. Photoreactor composition, method of generating a reactive species, and applications therefor
US6017661A (en) 1994-11-09 2000-01-25 Kimberly-Clark Corporation Temporary marking using photoerasable colorants
US6235095B1 (en) 1994-12-20 2001-05-22 Ronald Sinclair Nohr Ink for inkjet printers
US6063551A (en) 1995-06-05 2000-05-16 Kimberly-Clark Worldwide, Inc. Mutable dye composition and method of developing a color
US5681380A (en) 1995-06-05 1997-10-28 Kimberly-Clark Worldwide, Inc. Ink for ink jet printers
US5837429A (en) 1995-06-05 1998-11-17 Kimberly-Clark Worldwide Pre-dyes, pre-dye compositions, and methods of developing a color
US5786132A (en) 1995-06-05 1998-07-28 Kimberly-Clark Corporation Pre-dyes, mutable dye compositions, and methods of developing a color
US6033465A (en) 1995-06-28 2000-03-07 Kimberly-Clark Worldwide, Inc. Colorants and colorant modifiers
US5885337A (en) 1995-11-28 1999-03-23 Nohr; Ronald Sinclair Colorant stabilizers
US6168655B1 (en) 1995-11-28 2001-01-02 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US6099628A (en) 1996-03-29 2000-08-08 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5891229A (en) 1996-03-29 1999-04-06 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5782963A (en) 1996-03-29 1998-07-21 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US6168654B1 (en) 1996-03-29 2001-01-02 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US5855655A (en) 1996-03-29 1999-01-05 Kimberly-Clark Worldwide, Inc. Colorant stabilizers
US6524379B2 (en) 1997-08-15 2003-02-25 Kimberly-Clark Worldwide, Inc. Colorants, colorant stabilizers, ink compositions, and improved methods of making the same
US6503559B1 (en) 1998-06-03 2003-01-07 Kimberly-Clark Worldwide, Inc. Neonanoplasts and microemulsion technology for inks and ink jet printing
US6277897B1 (en) 1998-06-03 2001-08-21 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6228157B1 (en) 1998-07-20 2001-05-08 Ronald S. Nohr Ink jet ink compositions
US6265458B1 (en) 1998-09-28 2001-07-24 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6368396B1 (en) 1999-01-19 2002-04-09 Kimberly-Clark Worldwide, Inc. Colorants, colorant stabilizers, ink compositions, and improved methods of making the same
US6214766B1 (en) 1999-02-03 2001-04-10 Westvaco Corporation Security feature for paper products
US6331056B1 (en) 1999-02-25 2001-12-18 Kimberly-Clark Worldwide, Inc. Printing apparatus and applications therefor
US6294698B1 (en) 1999-04-16 2001-09-25 Kimberly-Clark Worldwide, Inc. Photoinitiators and applications therefor
US6368395B1 (en) 1999-05-24 2002-04-09 Kimberly-Clark Worldwide, Inc. Subphthalocyanine colorants, ink compositions, and method of making the same
WO2001005603A1 (en) * 1999-07-16 2001-01-25 Jury Viktorovich Zhvakoljuk Method for protecting information carriers against counterfeiting
US8397846B2 (en) 1999-09-15 2013-03-19 Hill-Rom Services, Inc. Patient support apparatus with powered wheel
US8240410B2 (en) 1999-09-15 2012-08-14 Hill-Rom Services, Inc. Patient support apparatus with powered wheel
US8267206B2 (en) 2000-05-11 2012-09-18 Hill-Rom Services, Inc. Motorized traction device for a patient support

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