US2710285A - Paper coating composition containing an optical brightener - Google Patents

Paper coating composition containing an optical brightener Download PDF

Info

Publication number
US2710285A
US2710285A US241404A US24140451A US2710285A US 2710285 A US2710285 A US 2710285A US 241404 A US241404 A US 241404A US 24140451 A US24140451 A US 24140451A US 2710285 A US2710285 A US 2710285A
Authority
US
United States
Prior art keywords
paper
wax
water
grams
added
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 - Lifetime
Application number
US241404A
Inventor
Ralf B Trusler
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DAVICS YOUNG SOAP Co
DAVICS-YOUNG SOAP Co
Original Assignee
DAVICS YOUNG SOAP Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by DAVICS YOUNG SOAP Co filed Critical DAVICS YOUNG SOAP Co
Priority to US241404A priority Critical patent/US2710285A/en
Application granted granted Critical
Publication of US2710285A publication Critical patent/US2710285A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP 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
    • D21H21/00—Non-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
    • D21H21/14—Non-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
    • D21H21/30—Luminescent or fluorescent substances, e.g. for optical bleaching
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP 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
    • D21H19/00—Coated paper; Coating material
    • D21H19/10—Coatings without pigments
    • D21H19/14—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/18—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising waxes

Definitions

  • This invention relates to paper coatings and, in particular, to increasing the brilliancy of a printed product by the application of a light reflecting coating increasing the brightness of the paper and increasing the contrast between the printing and the paper while, at the same time accomplishing a smooth, non-tacky finish that can be applied at high speed to paper sheets and paper strip after printing without bleeding or other deterioration of the printing or deterioration of the paper.
  • FIG. 1 shows a flow sheet for the treatment of paper, printed or unprinted by the compositions of this invention.
  • EXAMPLE #1 Ingredients: Grams Carnauba wax, refined 100.0 Oleic acid 15.0
  • EXAMPLE #2 Ingredients: Grams Carnauba wax #2 yellow 100.0 Oleic acid 12.0
  • the shellac (10.0 g.) was stirred in 100 ml. of water, to which was added the 5.0 g. of ammonia. The shellac dissolved to form a clear or nearly clear solution. This constituted part B.
  • Parts A and B were then mixed.
  • EXAMPLE #3 Ingredients: Grams Carnauba wax, refined 90.0 Parafiin wax, Grade Sun Oil Companys #5512 10.0 Oleic acid 14.0 Triethanolamine 10.0 Sodium salt of 4:4 dibenzoylamine-Stilbene 2:2 disulfonic acid 1.0
  • EXAMPLE #6 Ingredients: Grams Carnauba wax #2 Yellow 100.0 Oleic acid 13.0 lsopropanolamine 6.0 Borax 2.0 4 methyl 7 diethylamino coumarin 1.0 Water 900.0
  • EXAMPLE #7 Ingredients: Grams i Carnauba wax 80.0 Casein 20. Oleic acid 10.5 Isopropanolamine 5.0 Ammonia 26 4 methyl 7 diethylamino coumarin 1.0
  • the casein was rapidly stirred into 300 ml. of water to which then was added the ammonia. After a period of time the casein was dissolved producing a somewhat viscous solution. This constituted part B. Part A and part B were then mixed and any unused or additionally desired water was added. Ammonia in excess of the amount required to dissolve the casein acts as a preservative, and additional inhibitors may be added to this or the other examples to preserve them.
  • Example #2 requiring shellac provides for the use of water soluble sizing and body materials which are often useful in testuring fibrous surfaces and, in general, modifying wax containing surface coatings.
  • any one of my wax emulsion compositions can be further modified by incorporating a resinous, ingredient with the wax.
  • part of the carnauba wax may be replaced with resin of the type frequently used in varnish making, such as, modified rosin-malleic anhydride phenolic copolymers, the cumar resins, resins derived from terpenes and from pinenes and many others.
  • the resin and wax can be melted together and. then the resulting melt can be emulsified by the well known method of which Example 1 is typical.
  • Stilbene derivatives such as Blancophor manufactured by General Dyestuff Corporation, New York, New York; Fluorosol manufactured by the National Aniline Division, Allied Chemical and Dye Corp., New York, New York; Uvitex manufactured by Ciba Company, New York, New York; Tinopal manufactured by the Geigy Co., New York, New York; BMU manufactured by Koppers Co., Pittsburgh, Pennsylvania; and Calcofluor manufactured by American Cyanamid Co.
  • Other useful compounds are the fluorescent benzimidazoles and naphthylamines, thiazole derivatives, terephthalic acid derivatives, oxynaphthalene sulfonic acid and derivatives of anthraquinone.
  • the Blancophor compounds are based upon diaminostilbene compounds.
  • the fiuorosols are also based upon the stilbene derivatives.
  • the fluorosols are either oil soluble or water soluble. I have used successfully methyl umbelliferone manufactured by the Carlisle Company of Reading, Ohio. I prefer alpha benzyl B-methyl umbelliferone.
  • concentrations I prefer are 0.1% but they may range from 0.005% to 0.05%.
  • Hydroxycournarin may be used in place of betamethyl umbelliferone.
  • the amine soap formed by oleic acid and isopropanolamine, monoethanolarnine, triethanolamine acts as an emulsifier.
  • the use of borax assists in the emulsification as does ammonia. The borax controls penetration.
  • the paper stock 1 is printed at 2 either on continuous strip or on sheets and, upon the ink drying, the strip or sheets are immersed in a vat 3 containing the composition 4 of one of the examples.
  • This warm wax dispersion containing the brightening agent is maintained at a temperature of l C. to boiling (about C.) preferably between 25 C. and 60 C. Since the viscosities of the emulsions vary somewhat with temperature, generally being less and thinner at higher temperature degrees, the regulation of temperature degrees somewhat controls the amount of wax emulsion adhering to the paper prior to passing through the rollers 5.
  • the sheet is fed between rollers 5 for distributing the wax and applying pressure to the Wax surface of the paper.
  • the sheet is then fed through a dryer tunnel 6 Where a temperature or" approximately 140 F., plus or minus, is provided.
  • a temperature or approximately 140 F., plus or minus
  • a composition of matter for coating paper as set forth in claim 1, the step (a) of melting carnauba wax; the step (b) of adding oleic acid through the resultant melted wax and stirring the mixture; the step (c) of heating the mixture to 100 to C.; the step (d) of introducing into the heated mixture while stirring isopropanolamine diluted with hot water, the step (e) adding additional hot water to dilute the jelly-like mass; and the step (1) of introducing alpha benzyl B-methyl umbelliferone an optical brightening agent thereto while maintaining the mixture at a boil.

Description

Jun 7, 1955 B TRUSLER 2,710,285
R; PAPER COATING COMPOSITION CONTAINING AN OPTICAL BRIGHTENER Filed Aug. 11, 1951 INVENTOR RALF B. TRUSLER ATTORNEYS PAPER COATING COPOSITION CONTAINHJG AN OPTICAL BRIGHTENER Ralf B. Trnsler, Dayton, Ohio, assignor to The Davies- Young Soap Company, Dayton, Ohio, a corporation of Ohio Application August 11, 1051, Serial No. 241,404
2 Claims. (Cl. 252-3011) This invention relates to paper coatings and, in particular, to increasing the brilliancy of a printed product by the application of a light reflecting coating increasing the brightness of the paper and increasing the contrast between the printing and the paper while, at the same time accomplishing a smooth, non-tacky finish that can be applied at high speed to paper sheets and paper strip after printing without bleeding or other deterioration of the printing or deterioration of the paper.
In particular it is the object of this invention to provide for coatings that improve the light reflection of paper and printed paper and improve the contrast between the paper and the printing.
It is an object of this invention to provide such coating which may be applied to continuous sheets and strip as well as independent sheets and to provide a coating that prevents the sheets of paper from adhering to one another and causes them to be easily moved over one another when in engagement with one another. This is particularly desirable in connection with playing cards, books and the like.
It is a further object to provide a coating that will protect the coating of the surface of the paper and printing as well as increase the brilliancy of the light reflecting qualities of the article so treated.
It is a particular object of this invention to provide an optical bleach or light converter in wax coatings and to provide such a coating that it is substantive to the cellulose of the paper and ink on the paper.
It is a further object of the invention to provide such a coating on impervious surfaces.
In the case of playing cards, it is necessary to have flexible stock the surface of which is smooth, hard and permits the shuffling and dealing of the cards without deterioration or sticking. It is a further problem to be able to apply the coating at high speed with accuracy and without causing any damage to the brilliancy of the printing, but to the contrary, increase the brilliancy between the paper and the printing to facilitate the contrast between the printing and the paper.
Referring to the drawing, it shows a flow sheet for the treatment of paper, printed or unprinted by the compositions of this invention.
In order to carry out this invention, I have various compositions coming within the scope of my invention by which the following examples are typical:
EXAMPLE #1 Ingredients: Grams Carnauba wax, refined 100.0 Oleic acid 15.0
Isopropanolarnine 6.0 Alpha benzyl B methyl umbelliferone 1.0 Water, distilled 900.0
Method for cmbining.The carnauba wax was melted and theoleic acid was added and stirred, and brought to 100 to 110 C. The isopropanolamine was diluted with Ingredients:
, added with stirring to the melted wax.
2,710,235 Patented June 7, 1955 10 ml. of hot water and added with stirring to the melted wax. These ingredients produced a clear, jelly-like mass upon stirring. Hot water in portions of about 10 ml. were stirred into the mass until noticeable thinning occurred and at this stage, the one gram of alpha benzyl B methyl umbelliferone was added, all the time keeping the preparation boiling gently. When the latter compound had dissolved (about 3 minutes were required) the balance of the hot water was added with stirring. The
product was then ready to cool which can be accomplished by chilling the outside of the container.
EXAMPLE #2 Ingredients: Grams Carnauba wax #2 yellow 100.0 Oleic acid 12.0
Mono ethanolamine 5.0
B-methyl umbelliferone 1.0 Shellac 10.0
Ammonia 26 5.0
Water 1,000.0
Method for combining-The procedure for combining the carnauba wax, oleic acid, monoethanolamine, B-methyl umbelliferone and 900 ml. of water was similar to the method of Example #1, and this constituted part A.
The shellac (10.0 g.) was stirred in 100 ml. of water, to which was added the 5.0 g. of ammonia. The shellac dissolved to form a clear or nearly clear solution. This constituted part B.
Parts A and B were then mixed.
EXAMPLE #3 Ingredients: Grams Carnauba wax, refined 90.0 Parafiin wax, Grade Sun Oil Companys #5512 10.0 Oleic acid 14.0 Triethanolamine 10.0 Sodium salt of 4:4 dibenzoylamine-Stilbene 2:2 disulfonic acid 1.0
Distilled water 900.0
The method of combining these items was identical with the method of Example #1.
EXAMPLE #4 Grams Paraffin wax (Grade Sun Oil Co.s #5512) 100.00
Stearic acid 12.0 Monoethanolamine 5.0 B-methyl umbelliferone 1.0 Water 250.0
Method for c0mbining.--The parafiin wax and the stearic acid were melted together. The monoethanolamine was diluted with an equal amount of water and A thick paste resulted that could then be diluted with 50 ml. of hot water. Next, the methyl umbelliferone was thoroughly stirred into this preparation, and finally, the balance of the hot water (200 ml.) was gradually added during thorough stirring. The resultant emulsion of wax in water permitted further dilution at time of use.
' EXAMPLE 5 Ingredients: Grams Hydrogenated castor oil (melting point of 100.0 Oleic acid 15.0 Ethylethanolamine 10.0 B-methyl umbelliferone 1.0 Water 400.0
Method for combining-The hydrogenated castor oil was first melted and into this was stirred the oleic acid.
Twenty grams of water were mixed with the 10 g. of ethylethanolamine and this solution was stirred into the melted wax, followed by the addition of the B-methyl umbelliferone. Finally, the water was added, about 10 ml. at a time until 100 ml. were used. Then, the balance was all in. This wax emulsion, like the others, was diluted with water to attain a 10 to 12% solids (in suspension) for use.
EXAMPLE #6 Ingredients: Grams Carnauba wax #2 Yellow 100.0 Oleic acid 13.0 lsopropanolamine 6.0 Borax 2.0 4 methyl 7 diethylamino coumarin 1.0 Water 900.0
EXAMPLE #7 Ingredients: Grams i Carnauba wax 80.0 Casein 20. Oleic acid 10.5 Isopropanolamine 5.0 Ammonia 26 4 methyl 7 diethylamino coumarin 1.0
Water 875.0
Method for combining-The carnauba wax was melted and to it was added the oleic acid with stirring. lsopropanolamine, diluted with some water was next added, followed by the 4 methyl 7 diethylamino coumarin. Finally, this was diluted with 500 ml. of soft water. The method for this step is similar to that described in Example #1. This part constituted part-A.
The casein was rapidly stirred into 300 ml. of water to which then was added the ammonia. After a period of time the casein was dissolved producing a somewhat viscous solution. This constituted part B. Part A and part B were then mixed and any unused or additionally desired water was added. Ammonia in excess of the amount required to dissolve the casein acts as a preservative, and additional inhibitors may be added to this or the other examples to preserve them.
This preparation, and also that of Example #2 requiring shellac provides for the use of water soluble sizing and body materials which are often useful in testuring fibrous surfaces and, in general, modifying wax containing surface coatings.
Any one of my wax emulsion compositions can be further modified by incorporating a resinous, ingredient with the wax. For example, part of the carnauba wax may be replaced with resin of the type frequently used in varnish making, such as, modified rosin-malleic anhydride phenolic copolymers, the cumar resins, resins derived from terpenes and from pinenes and many others. The resin and wax can be melted together and. then the resulting melt can be emulsified by the well known method of which Example 1 is typical.
Method for combining-First, the carnauba wax was melted and when it was at 110 C., the oleic acid was stirred into it and the heating was discontinued. The isopropanolamine was diluted with 12 ml. of water and then poured slowly into the melted wax with stirring. Next, the borax, which had been dissolved in 5 ml. of hot water, was also stirred into the wax. At this stage the one gram of 4 methyl 7 diethylamino coumarin was next added followed by 10 ml. portions of hot water until 50 ml. were added. Hot water was then added in ml. portions with stirring, until a total of 200 ml. were used. Then, the balance was poured in.
Optical brighteners I find that 0.1% furnishes a satisfactory quantity of brightener. Such products as the following will be found useful:
Stilbene derivatives such as Blancophor manufactured by General Dyestuff Corporation, New York, New York; Fluorosol manufactured by the National Aniline Division, Allied Chemical and Dye Corp., New York, New York; Uvitex manufactured by Ciba Company, New York, New York; Tinopal manufactured by the Geigy Co., New York, New York; BMU manufactured by Koppers Co., Pittsburgh, Pennsylvania; and Calcofluor manufactured by American Cyanamid Co.
I have found useful coumarin and stilbene derivatives. Other useful compounds are the fluorescent benzimidazoles and naphthylamines, thiazole derivatives, terephthalic acid derivatives, oxynaphthalene sulfonic acid and derivatives of anthraquinone. The Blancophor compounds are based upon diaminostilbene compounds. The fiuorosols are also based upon the stilbene derivatives. The fluorosols are either oil soluble or water soluble. I have used successfully methyl umbelliferone manufactured by the Carlisle Company of Reading, Ohio. I prefer alpha benzyl B-methyl umbelliferone.
The concentrations I prefer are 0.1% but they may range from 0.005% to 0.05%.
Hydroxycournarin may be used in place of betamethyl umbelliferone.
The amine soap formed by oleic acid and isopropanolamine, monoethanolarnine, triethanolamine acts as an emulsifier. The use of borax assists in the emulsification as does ammonia. The borax controls penetration.
Method of application The paper stock 1 is printed at 2 either on continuous strip or on sheets and, upon the ink drying, the strip or sheets are immersed in a vat 3 containing the composition 4 of one of the examples. This warm wax dispersion containing the brightening agent is maintained at a temperature of l C. to boiling (about C.) preferably between 25 C. and 60 C. Since the viscosities of the emulsions vary somewhat with temperature, generally being less and thinner at higher temperature degrees, the regulation of temperature degrees somewhat controls the amount of wax emulsion adhering to the paper prior to passing through the rollers 5. The sheet is fed between rollers 5 for distributing the wax and applying pressure to the Wax surface of the paper. The sheet is then fed through a dryer tunnel 6 Where a temperature or" approximately 140 F., plus or minus, is provided. When the coating is dry, the sheet is passed between polishing rollers 7 which give a light kiss to the sheet to polish the wax coating and thence between final brushes 8 for completing the operation.
It will be understood that I desire to comprehend within the following claims such variations and adaptations of my invention which may be found necessary in applying to various industrial conditions and requirements.
I claim:
1. In a new composition of matter for surface coating of paper, the combination of carnauba wax, refined, 100.0 grams; oleic acid, 15.0 grams; isopropanolamine, 6.0 grams; alpha benzyl B-methyl umbelliferone, 1.0 grams; and water, distilled, 900.0 grams.
2. In a method of manufacturing a composition of matter for coating paper as set forth in claim 1, the step (a) of melting carnauba wax; the step (b) of adding oleic acid through the resultant melted wax and stirring the mixture; the step (c) of heating the mixture to 100 to C.; the step (d) of introducing into the heated mixture while stirring isopropanolamine diluted with hot water, the step (e) adding additional hot water to dilute the jelly-like mass; and the step (1) of introducing alpha benzyl B-methyl umbelliferone an optical brightening agent thereto while maintaining the mixture at a boil.
flleferences on following page) References Cited in the file of this patent UNITED STATES PATENTS Axelrad Feb. 8, 1944 Cartwright Apr. 24, 1945 Thomas Oct. 31, 1950 Schoenholz Jan. 2, 1951 Porter Feb. 6, 1951 6 FOREIGN PATENTS Great Britain June 24, 1940 OTHER REFERENCES

Claims (1)

1. IN A NEW COMPOSITION OF MATTER FOR SURFACE COATING OF PAPER, THE COMBINATION OF CARNAUBA WAX, REFINED, 100.0 GRAMS: OLEIC ACID, 15.0 GRAMS; ISOPROPANOPANLAMINE, 6.0 GRAMS; ALPHA BENZYL B-METHYL UMBELLIFERONE, 1.0 GRAMS; AND WATER, DISTILLED, 900.0 GRAMS.
US241404A 1951-08-11 1951-08-11 Paper coating composition containing an optical brightener Expired - Lifetime US2710285A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US241404A US2710285A (en) 1951-08-11 1951-08-11 Paper coating composition containing an optical brightener

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US241404A US2710285A (en) 1951-08-11 1951-08-11 Paper coating composition containing an optical brightener

Publications (1)

Publication Number Publication Date
US2710285A true US2710285A (en) 1955-06-07

Family

ID=22910562

Family Applications (1)

Application Number Title Priority Date Filing Date
US241404A Expired - Lifetime US2710285A (en) 1951-08-11 1951-08-11 Paper coating composition containing an optical brightener

Country Status (1)

Country Link
US (1) US2710285A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2772967A (en) * 1954-06-28 1956-12-04 American Cyanamid Co Sized paper
US2822288A (en) * 1955-04-29 1958-02-04 Kee Lox Mfg Company Luminescent transfer paper
US3001963A (en) * 1959-06-22 1961-09-26 Continental Oil Co Non-foaming wax composition
US3892675A (en) * 1973-01-23 1975-07-01 Ici Ltd Coating compositions
US4751020A (en) * 1985-11-15 1988-06-14 Henkel Kommanditgesellschaft Auf Aktien UV-fluorescent cyanoacrylate adhesive
WO1994018272A1 (en) * 1993-02-05 1994-08-18 The Mead Corporation Recyclable wax-coated containers
US5539035A (en) * 1994-10-12 1996-07-23 The Mead Corporation Recyclable wax-coated containers
US6030443A (en) * 1999-04-29 2000-02-29 Hercules Incorporated Paper coating composition with improved optical brightener carriers
US20030166766A1 (en) * 1999-12-17 2003-09-04 Leyrer Reinhold J. Paper coating material with elevated water retention
US20150030874A1 (en) * 2011-09-23 2015-01-29 Lucas-Milhaupt, Inc. Luminescent Braze Preforms

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB522672A (en) * 1939-06-02 1940-06-24 Meyer Hans Treating articles, substances or materials of a yellowish or off-white tint so as to obtain a pure white appearance
US2341009A (en) * 1936-03-19 1944-02-08 Richards Chemical Works Method of improving brightness of fibrous materials
US2374414A (en) * 1942-06-25 1945-04-24 Foster D Snell Inc Polishing composition
US2528324A (en) * 1945-04-12 1950-10-31 Lever Brothers Ltd Method of treating paper and the resulting products
US2536018A (en) * 1948-06-16 1951-01-02 Schoenholz Daniel Coating compositions
US2541006A (en) * 1947-11-18 1951-02-06 American Cyanamid Co Modified petroleum sulfonates as emulsifying agents for waxes

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2341009A (en) * 1936-03-19 1944-02-08 Richards Chemical Works Method of improving brightness of fibrous materials
GB522672A (en) * 1939-06-02 1940-06-24 Meyer Hans Treating articles, substances or materials of a yellowish or off-white tint so as to obtain a pure white appearance
US2374414A (en) * 1942-06-25 1945-04-24 Foster D Snell Inc Polishing composition
US2528324A (en) * 1945-04-12 1950-10-31 Lever Brothers Ltd Method of treating paper and the resulting products
US2541006A (en) * 1947-11-18 1951-02-06 American Cyanamid Co Modified petroleum sulfonates as emulsifying agents for waxes
US2536018A (en) * 1948-06-16 1951-01-02 Schoenholz Daniel Coating compositions

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2772967A (en) * 1954-06-28 1956-12-04 American Cyanamid Co Sized paper
US2822288A (en) * 1955-04-29 1958-02-04 Kee Lox Mfg Company Luminescent transfer paper
US3001963A (en) * 1959-06-22 1961-09-26 Continental Oil Co Non-foaming wax composition
US3892675A (en) * 1973-01-23 1975-07-01 Ici Ltd Coating compositions
US4751020A (en) * 1985-11-15 1988-06-14 Henkel Kommanditgesellschaft Auf Aktien UV-fluorescent cyanoacrylate adhesive
WO1994018272A1 (en) * 1993-02-05 1994-08-18 The Mead Corporation Recyclable wax-coated containers
US5539035A (en) * 1994-10-12 1996-07-23 The Mead Corporation Recyclable wax-coated containers
US6030443A (en) * 1999-04-29 2000-02-29 Hercules Incorporated Paper coating composition with improved optical brightener carriers
US20030166766A1 (en) * 1999-12-17 2003-09-04 Leyrer Reinhold J. Paper coating material with elevated water retention
US20040214941A1 (en) * 1999-12-17 2004-10-28 Basf Aktiengesellschaft Paper coating slips having high water retention
US6964993B2 (en) 1999-12-17 2005-11-15 Basf Aktiengesellschaft Paper coating slip containing polyvinyl alcohol as a protective colloid
US20150030874A1 (en) * 2011-09-23 2015-01-29 Lucas-Milhaupt, Inc. Luminescent Braze Preforms

Similar Documents

Publication Publication Date Title
US2710285A (en) Paper coating composition containing an optical brightener
US3477970A (en) Pigmented paper coating and adhesive compositions containing a polyvinyl alcohol binder and a modifier therefor
JP2002512321A (en) Lubricant for paper coating
US2348687A (en) Composition for coating and laminating sheet materials
US2536018A (en) Coating compositions
US3928707A (en) Paper coating lubricants and coated paper incorporating such
US2544146A (en) Adhesive composition for metal foil to paper laminating
US2371473A (en) Wax composition
EP0713548B1 (en) Paper or carboard with a coating applied by cast coating, process for producing the same and its use
US2387773A (en) Hot-melt coating composition
US2394233A (en) Coating compositions
US2319957A (en) Coated paper
US2234934A (en) Wax suspension
US2340846A (en) Wax emulsion
US3736164A (en) Organophobic and hydrophobic surface coatings
JPS62158768A (en) Low friction falling newspaper ink
DE2628571A1 (en) METHOD FOR IMPROVING THE EFFECT OF OPTICAL BRIGHTENERS IN THE PAPER INDUSTRY
US2234648A (en) Process of making colored paper
US2177580A (en) Process of coating paper
US1293983A (en) Stencil-paper and compounds and method for making them.
US1439696A (en) Ink
US2810656A (en) Zein water emulsion
US2369427A (en) Paper coating composition and method of making
US2387774A (en) Hot melt coating composition
US2114985A (en) Coating composition