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US2360252A - Dry mounting tissue - Google Patents

Dry mounting tissue Download PDF

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Publication number
US2360252A
US2360252A US422690A US42269041A US2360252A US 2360252 A US2360252 A US 2360252A US 422690 A US422690 A US 422690A US 42269041 A US42269041 A US 42269041A US 2360252 A US2360252 A US 2360252A
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Prior art keywords
adhesive
tissue
cellulose
paper
dry mounting
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Expired - Lifetime
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US422690A
Inventor
Carl J Malm
Gordon D Hiatt
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Eastman Kodak Co
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Eastman Kodak Co
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Priority to US422690A priority Critical patent/US2360252A/en
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J101/00Adhesives based on cellulose, modified cellulose, or cellulose derivatives
    • C09J101/08Cellulose derivatives
    • C09J101/10Esters of organic acids
    • C09J101/14Mixed esters, e.g. cellulose acetate-butyrate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0016Plasticisers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L35/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L35/02Homopolymers or copolymers of esters
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S264/00Plastic and nonmetallic article shaping or treating: processes
    • Y10S264/73Processes of stretching
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2813Heat or solvent activated or sealable
    • Y10T428/2817Heat sealable
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2813Heat or solvent activated or sealable
    • Y10T428/2817Heat sealable
    • Y10T428/2826Synthetic resin or polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2852Adhesive compositions
    • Y10T428/2865Adhesive compositions including monomer or polymer of carbohydrate [e.g., starch, dextrin, etc.] Or protein [e.g., casein, animal protein, etc.] Or derivative thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • Y10T428/2852Adhesive compositions
    • Y10T428/2878Adhesive compositions including addition polymer from unsaturated monomer

Definitions

  • This invention relates to dry mounting tissue and more particularly to improved adhesives for use on dry mounting tissue.
  • Dry mounting tissue is usually composed of a thin semi-transparent paper support coated on both sides with a thermoplastic adhesive. In mounting photographs or other articles on a suitable mounting such dry mounting tissue is placed between the photograph and the mount, and heat and pressure are applied to cause the adhesive to flow. On cooling, the photograph will remain firmly adhered to the mount.
  • the usual expedient is to interleave the adhesive coated sheets with waxed tissue paper before packaging. This of course adds to the cost of production both in materials and in operations.
  • An object of the present invention is, therefore, an improved non-blocking type of dry mounting tissue.
  • Another object is a dry mounting tissue which may be packaged without the need of interleaving sheets between adjacent dry mounting adhesive tissues.
  • a further object of the invention is an adhesive suitable for use on dry mounting tissue which makes possible instant adherence of materials at elevated temperatures and quick setting of the adhesive upon relatively slight cooling.
  • a still further object of the invention is an adhesive material which is substantially inert at ordinary temperatures and will not adhere to surfaces brought in contact with it at those temperatures.
  • an adhesive composition containing a cellulose organic acid ester, and synthetic resin "and, a plasticizer and coating it on both sides of thin tissue paper, or an equivalent support, to form the dry mounting tissue.
  • the composition may be coated on the support from a solvent solution or by a melt coating process.
  • the more desirable compositions contain a larger proportion of the cellulose ester and a smaller proportion of the resin.
  • cellulose organic acid ester containing a relatively high percentage of propionyl, butyryl or higher acyl groups, or a mixed organic acid ester in which the propionyl, butyryl or higher acyl groups predominate over the lower acyl groups, usually acetyl.
  • Very useful cellulose esters are those included on the shaded areas on the accompanying drawing, Figs. 1 and 2, of triangular graphs.
  • the triangular graph identified as Fig. 1 shows the area of the most useful cellulose propionates and cellulose acetate propionates.
  • the graph identified as Fig. 2 gives similar information on cellulose butyrates and cellulose acetate butyrates.
  • the straight lines identified as dd' and t-t on these graphs represent the diester lines and the triester lines respectively. Lines A and B bound the ester compounds which may be employed in our novel adhesive.
  • Curved line C encompasses the compositions particularly suitable for use as an adhesive
  • curved line D encompasses substantially all the compositions which may be so employed.
  • the preferred compositions contain a larger proportion of ester to a smaller proportion of resin.
  • the viscosity of the ester should be preferably quite low since this permits coating from concentrated solutions and further lowers the melting or sealing temperature of the composition. This will be evident from the following table showing change in melting point with change in viscosity in a cellulose acetate butyrate of 38% butyryl and 12% acetyl content.
  • Viscosity 1 Cellulose ester 10% solids g fl in acetone p C'ps. C. High viscosity 200 190 Low viscosity 8 170 It will be understood that the higher-viscosity cellulose ester may be employed, if desired, but the lower viscosity esters as the base of the adhesive make a better product. These esters melt in general at or below 210 C. and are compatible with the resin employed. The compositions shown on the graphs heat seal below 250 F. and do not exhibit tackiness below F. The ester should contain at least 43% total acyl of which a majority oi the acyl consists of groups of 3 carbons or more.
  • plasticizers for use with this type of cellulose ester and synthetic resin are diethyl phthalate, dibutyl phthalate, Other useful plasticizers are dibutyl sebacate, diamyl phthalate, triethyleneglycol dipropionate.
  • Example 1 An adhesive composition in solution is made by mixing 60 parts of cellulose acetatebutyrate, containing 38 butyryl and 12% acetyl, with 20 parts of dibutyl phthalate and 20 parts of Petrex 21 resin in a 2:1 benzene-denatured alcohol solvent.
  • a dry mounting tissue is formed by coating this solution on glassine paper under conditions permitting the solvents to evaporate uniformly.
  • the dope solution is coated on both sides of the glassine paper by feeding the paper into a pan of the dope. Curing is carried out by passing the paper slowly up through a heated tower. The solvent is thus removed, and the cured paper is gathered on a roll. The cured product is not tacky at room temperatures but will bind a photographic print securely to a mounting board at 200-220 F.
  • the mounting operation may be conducted in the usual manner i. e. by placing the mounting tssue between the back of the photograph and the mounting and pressing with an electric iron maintained at the 200-220 F.
  • Example 2 An adhesive composition in solution is made by mixing 12.6 parts of cellulose acetate butyrate of 14.4% ace-tyl and 36.4% butyryl content, 3.7 parts of Petrex 21 resin, and 4.6 parts of diethyl phthalate in 116 parts of 3:1 benzene denatured alcohol solvent. This solution is coated on tissue paper by dipping the paper in the solution. The paper is then dried to expel the solvent mixture.
  • Example 4 butyryl radicals, as above suggested, higher fatty esters, for example, the acetate stearates may be employed as shown in the following example.
  • Example 5 A cellulose acetate stearate analyzing 17.9% acetyl and 43.9% stearyl and melting at 145 C. was employed in a heat sealing composition. also containing Petrex 21 resin and diethyl pththalate. The ratio of cellulose ester: resin: plasticizer is 60:14:26. This composition when coated on glassine paper gives good bonding at 220 F.
  • cellulose ester Petrex 21" resin adhesive compositions for dry mounting tissues have several advantages not found in previous dry mounting tissue adhesives. They are non-tacky and non-blocking so that, interleaving with paper is not necessary. While having the improved adhesiveness of a soft resin, they do not have the tackiness of a soft resin adhesive at lower temperatures.
  • the incorporation of the plasticizer permits close adjustment of the elevated temperature at which the adhesive becomes tacky for dry mounting purposes.
  • the use of low viscosity cellulose esters as the base of the adhesive permits fiow' only at elevated temperatures.
  • these compositions show good strength above their melting temperature so that the photographic print is held firmly to the mount even though the composition is in a fluid state. This allows the mounting iron to be removed without th print curling from the mounting board.
  • a dry mounting tissue comprising a sheet of thin tissue-like supporting material having on each side thereof a coating of an adhesive composition containing as essential elements of the adhesive composition a cellulose acetate butyra-te, a compatible plasticizer, and an alkyd resin constituting a terpinene-maleic anhydride condensate reacted with a glycol, the proportions of the three components of the said adhesive compositime being those represented by any point falling within the area designated as D in Fig. 3 of the accompanying drawing and the cellulose acetate butyrate having an acetyl and a butyryl content represented by any point falling Within the area designated as B in Fig. 2 of the accompanying drawing, said composition being characterized in that it heat seals at a temperature between 125 F. and 250 F. and is free from tackiness at a temperature below 125 F.
  • a dry mounting tissue comprising a sheet of thin tissue-like supporting material having on each side thereof a coating of an adhesive composition containing as essential elements of the adhesive composition a cellulose acetat butyrate, a compatible plasticizer, and an alkyd resin constituting a terpinene-maleic anhydride condensate reacted with a glycol, the proportions of the three components of the said. adhesive composition being those represented by any point falling within the area designated as C in Fig. 3 of the accompanying drawing and the cellulose acetate butyrate having an acetyl and a butyr l content represented by any point falling within the area designated as B in Fig. 2 of the accompanying drawing, said composition being characterized in that it heat seals at a temperature between 125 F. and 250 F. and is free from tackiness at a temperature below 125 F.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

Oct. 10, 1944. MALM HAL 2,360,252
DRY MOUNTING TISSUE Filed Dec. 12, 1941 CELLULOSE v v A AA V V'V'A'AYA CARL J. MALM GORDON D. HL4TT INVENTORS I 221w IM YfiMJ-W D C A RNEYS Patented Oct. 10, 1944 DRY MOUNTING TISSUE Carl J. Malm and Gordon D. Hiatt, Rochester,
N. Y., assignors to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey Application December 12, 1941, Serial No. 422,690
2 Claims.
This invention relates to dry mounting tissue and more particularly to improved adhesives for use on dry mounting tissue.
Dry mounting tissue is usually composed of a thin semi-transparent paper support coated on both sides with a thermoplastic adhesive. In mounting photographs or other articles on a suitable mounting such dry mounting tissue is placed between the photograph and the mount, and heat and pressure are applied to cause the adhesive to flow. On cooling, the photograph will remain firmly adhered to the mount.
In making mounting tissue which has an adhesive coating on both sides the problem of packaging the mounting tissue so that it may be easily dispensed is a difficult one since the adjacent sheets tend to adhere together or "block" in the package. The sheets are thus difllcult to separate and in some cases if stored at warm temperatures are inseparable.
The usual expedient is to interleave the adhesive coated sheets with waxed tissue paper before packaging. This of course adds to the cost of production both in materials and in operations.
An object of the present invention is, therefore, an improved non-blocking type of dry mounting tissue.
Another object is a dry mounting tissue which may be packaged without the need of interleaving sheets between adjacent dry mounting adhesive tissues.
A further object of the invention is an adhesive suitable for use on dry mounting tissue which makes possible instant adherence of materials at elevated temperatures and quick setting of the adhesive upon relatively slight cooling.
A still further object of the invention is an adhesive material which is substantially inert at ordinary temperatures and will not adhere to surfaces brought in contact with it at those temperatures.
In accordance with the invention these .and other objects are attained by forming an adhesive composition containing a cellulose organic acid ester, and synthetic resin "and, a plasticizer and coating it on both sides of thin tissue paper, or an equivalent support, to form the dry mounting tissue. The composition may be coated on the support from a solvent solution or by a melt coating process. The more desirable compositions contain a larger proportion of the cellulose ester and a smaller proportion of the resin.
We preferably employ a cellulose organic acid ester containing a relatively high percentage of propionyl, butyryl or higher acyl groups, or a mixed organic acid ester in which the propionyl, butyryl or higher acyl groups predominate over the lower acyl groups, usually acetyl.
Very useful cellulose esters are those included on the shaded areas on the accompanying drawing, Figs. 1 and 2, of triangular graphs. The triangular graph identified as Fig. 1 shows the area of the most useful cellulose propionates and cellulose acetate propionates. The graph identified as Fig. 2 gives similar information on cellulose butyrates and cellulose acetate butyrates. The straight lines identified as dd' and t-t on these graphs represent the diester lines and the triester lines respectively. Lines A and B bound the ester compounds which may be employed in our novel adhesive. The graph identified as Fig. 3 shows the preferred and acceptable compositions of cellulose esters and Petrex 21" resin which may be used in forming the adhesive especially when employing acetate butyrates of 3641% butyryl and 8-14% acetyl. Curved line C encompasses the compositions particularly suitable for use as an adhesive, and curved line D encompasses substantially all the compositions which may be so employed. As above stated, it will be noted from this graph that the preferred compositions contain a larger proportion of ester to a smaller proportion of resin.
The viscosity of the ester should be preferably quite low since this permits coating from concentrated solutions and further lowers the melting or sealing temperature of the composition. This will be evident from the following table showing change in melting point with change in viscosity in a cellulose acetate butyrate of 38% butyryl and 12% acetyl content.
Viscosity 1 Cellulose ester 10% solids g fl in acetone p C'ps. C. High viscosity 200 190 Low viscosity 8 170 It will be understood that the higher-viscosity cellulose ester may be employed, if desired, but the lower viscosity esters as the base of the adhesive make a better product. These esters melt in general at or below 210 C. and are compatible with the resin employed. The compositions shown on the graphs heat seal below 250 F. and do not exhibit tackiness below F. The ester should contain at least 43% total acyl of which a majority oi the acyl consists of groups of 3 carbons or more.
and dioctyl phthala'te.
blocking resins.
We hav found that suitable plasticizers for use with this type of cellulose ester and synthetic resin are diethyl phthalate, dibutyl phthalate, Other useful plasticizers are dibutyl sebacate, diamyl phthalate, triethyleneglycol dipropionate.
The invention will be more clearly understood by reference to the following examples.
Example 1 An adhesive composition in solution is made by mixing 60 parts of cellulose acetatebutyrate, containing 38 butyryl and 12% acetyl, with 20 parts of dibutyl phthalate and 20 parts of Petrex 21 resin in a 2:1 benzene-denatured alcohol solvent.
A dry mounting tissue is formed by coating this solution on glassine paper under conditions permitting the solvents to evaporate uniformly.
The dope solution is coated on both sides of the glassine paper by feeding the paper into a pan of the dope. Curing is carried out by passing the paper slowly up through a heated tower. The solvent is thus removed, and the cured paper is gathered on a roll. The cured product is not tacky at room temperatures but will bind a photographic print securely to a mounting board at 200-220 F. The mounting operation may be conducted in the usual manner i. e. by placing the mounting tssue between the back of the photograph and the mounting and pressing with an electric iron maintained at the 200-220 F.
temperature.
Example 2 An adhesive composition in solution is made by mixing 12.6 parts of cellulose acetate butyrate of 14.4% ace-tyl and 36.4% butyryl content, 3.7 parts of Petrex 21 resin, and 4.6 parts of diethyl phthalate in 116 parts of 3:1 benzene denatured alcohol solvent. This solution is coated on tissue paper by dipping the paper in the solution. The paper is then dried to expel the solvent mixture.
It was found that this coating was not tacky at A thin, homogeneous melt is made of 60 parts of a cellulose acetate butyrate containing 38% butyryl and 12% actyl, 30 parts of dioctyl ph-thalate and 10 parts Petrex 21 resin by stirring at 180 C. The melt was applied in a thin layer to glassine paper by the use of an applicator roll and a doctor blade. The melted surface quickly sets so that the coated paper may be wound up on a roll. The resulting mounting tissue was found to satisfactorily bind photographs to mounts at a temperature of 200-220 F.
Example 4 butyryl radicals, as above suggested, higher fatty esters, for example, the acetate stearates may be employed as shown in the following example.
Example 5 A cellulose acetate stearate analyzing 17.9% acetyl and 43.9% stearyl and melting at 145 C. was employed in a heat sealing composition. also containing Petrex 21 resin and diethyl pththalate. The ratio of cellulose ester: resin: plasticizer is 60:14:26. This composition when coated on glassine paper gives good bonding at 220 F.
but shows no tack at 125 F.
In addition to making satisfactory seals within a practical temperature range these adhesive compositions do not block when packaged without interleaving waxed paper.
The storage characteristics of these sheets were tested by placing a plurality of the coated sheets in layers and subjecting them to a pressure of 1 /2 lbs. per square inch at F. for 12 hours. It has been found that if the sheets do not stick together or block after this treatment they can be safely packaged without interleaving wax paper. I
The above described cellulose ester Petrex 21" resin adhesive compositions for dry mounting tissues have several advantages not found in previous dry mounting tissue adhesives. They are non-tacky and non-blocking so that, interleaving with paper is not necessary. While having the improved adhesiveness of a soft resin, they do not have the tackiness of a soft resin adhesive at lower temperatures. The incorporation of the plasticizer permits close adjustment of the elevated temperature at which the adhesive becomes tacky for dry mounting purposes. The use of low viscosity cellulose esters as the base of the adhesive permits fiow' only at elevated temperatures. In addition these compositions show good strength above their melting temperature so that the photographic print is held firmly to the mount even though the composition is in a fluid state. This allows the mounting iron to be removed without th print curling from the mounting board.
In the folowing claims where reference is made to compositions described by the curves of the attached drawing, it will be understood that these compositions are those within the shaded areas demarked by the respectiv curves.
We claim:
1. A dry mounting tissue comprising a sheet of thin tissue-like supporting material having on each side thereof a coating of an adhesive composition containing as essential elements of the adhesive composition a cellulose acetate butyra-te, a compatible plasticizer, and an alkyd resin constituting a terpinene-maleic anhydride condensate reacted with a glycol, the proportions of the three components of the said adhesive compositime being those represented by any point falling within the area designated as D in Fig. 3 of the accompanying drawing and the cellulose acetate butyrate having an acetyl and a butyryl content represented by any point falling Within the area designated as B in Fig. 2 of the accompanying drawing, said composition being characterized in that it heat seals at a temperature between 125 F. and 250 F. and is free from tackiness at a temperature below 125 F.
2. A dry mounting tissue comprising a sheet of thin tissue-like supporting material having on each side thereof a coating of an adhesive composition containing as essential elements of the adhesive composition a cellulose acetat butyrate, a compatible plasticizer, and an alkyd resin constituting a terpinene-maleic anhydride condensate reacted with a glycol, the proportions of the three components of the said. adhesive composition being those represented by any point falling within the area designated as C in Fig. 3 of the accompanying drawing and the cellulose acetate butyrate having an acetyl and a butyr l content represented by any point falling within the area designated as B in Fig. 2 of the accompanying drawing, said composition being characterized in that it heat seals at a temperature between 125 F. and 250 F. and is free from tackiness at a temperature below 125 F.
CARL J. MALM. GORDON D. HIA'IIT.
US422690A 1941-12-12 1941-12-12 Dry mounting tissue Expired - Lifetime US2360252A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2445553A (en) * 1945-11-30 1948-07-20 Resinous Prod & Chemical Co Pressure-sensitive adhesive sheet
WO2015167758A1 (en) * 2014-04-28 2015-11-05 Celanese Acetate Llc Adhesives that include highly-plasticized cellulose esters and methods and articles relating thereto
WO2015191973A1 (en) * 2014-06-12 2015-12-17 Celanese Acetate Llc Liquid cellulose ester adhesives
WO2015191153A1 (en) * 2014-06-12 2015-12-17 Celanese Acetate Llc Highly-plasticized cellulose acetate adhesives
WO2015191525A1 (en) * 2014-06-12 2015-12-17 Celanese Acetate Llc Adhesives that include highly-plasticized cellulose esters and methods and articles relating thereto

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2445553A (en) * 1945-11-30 1948-07-20 Resinous Prod & Chemical Co Pressure-sensitive adhesive sheet
WO2015167758A1 (en) * 2014-04-28 2015-11-05 Celanese Acetate Llc Adhesives that include highly-plasticized cellulose esters and methods and articles relating thereto
WO2015191973A1 (en) * 2014-06-12 2015-12-17 Celanese Acetate Llc Liquid cellulose ester adhesives
WO2015191153A1 (en) * 2014-06-12 2015-12-17 Celanese Acetate Llc Highly-plasticized cellulose acetate adhesives
WO2015191525A1 (en) * 2014-06-12 2015-12-17 Celanese Acetate Llc Adhesives that include highly-plasticized cellulose esters and methods and articles relating thereto

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