Eastman Chemical Company

Synthomer Adhesive Technologies LLC

Gary Robert Robe

Marc Stacey Somers

Mutombo Joseph Muvundamina

Raymond Prescott Cottle

Bennett H Novak

Andrea Gail Hagood

Dhiraj Sudesh Sood

Timothy Williams

Max Allen Weaver

Michael Eugene Donelson

Scott Ellery George

Marcus David Shelby

Brian Edison Maxwell

Freddie Wayne Williams

Rajesh Puthenkovilakom Raja

Joshua Seth Cannon

Richard A Miller

Puthenkovilakom Rajesh Raja

Candace Michele Tanner

Jeremy Richard Lizotte

Emmett Patrick O'Brien

Anthony Joseph Pasquale

Amorphous propylene-ethylene copolymers are described herein that can include high amounts of ethylene and exhibit desirable softening points and needle penetrations. The desirable combinations of softening points and needle penetrations in these propylene-ethylene copolymers allow them to have a broad operating window. Due their broad operating window, the propylene-ethylene copolymers can be utilized in a wide array of applications and products, including hot melt adhesives.

Amorphous propylene-ethylene copolymers

Adhesives comprising amorphous propylene-ethylene copolymers

A low molecular weight copolymer is provided comprising propylene and ethylene,

Disclosed are hot-melt adhesives prepared from aromatic-aliphatic polyesters containing terephthalic acid in combination with adipic acid, glutaric acid, or a mixture thereof, as diacid components and a diol component containing 1,4-butanediol, 1,6-hexanediol, or a combination thereof. These adhesives set up rapidly within a well-defined temperature window. The hot-melt adhesives can be used in a variety of applications, but are especially suited as seaming adhesives for roll-applied labels. These adhesives have melting temperatures and crystallization properties that allow their application at temperatures cool enough to prevent curling and premature shrinkage of the shrink label during seaming, and yet produce strong label seams that can withstand the elevated temperatures of a shrink tunnel without sacrificing line speed. Also disclosed are labeled containers and a process for applying a roll-on, shrink label to a container using the hot-melt adhesives of the invention.

Aromatic-aliphatic polyester hot melt adhesives for roll-applied labels

Disclosed are hot-melt adhesives prepared from polyesters containing 1,4-cyclohexane-dicarboxylic acid as a diacid component and a diol component containing at least two diols chosen from 1,4-cyclohexanedimethanol, triethylene glycol, and diethylene glycol. These adhesives set up rapidly within a well-defined temperature window. The hot-melt adhesives can be used in a variety of applications, but are especially suited as seaming adhesives for roll-applied labels. These adhesives have melting temperatures and crystallization properties that allow their application at temperatures cool enough to prevent curling and premature shrinkage of the shrink label during seaming, and yet produce strong label seams that can withstand the elevated temperatures of a shrink tunnel without sacrificing line speed. Also disclosed are labeled containers and a process for applying a roll-on, shrink label to a container using the hot-melt adhesives of the invention.

Hot melt adhesives for roll-applied labels

A composition comprising a hot melt adhesive; and a coating for the adhesive comprising cellulose acetate butyrate, wherein the cellulose acetate butyrate is coated on the hot melt adhesive, and a method to prevent blocking of hot melt adhesives comprising coating cellulose acetate butyrate on at least a portion of the surface of a hot melt adhesive.

Anti-blocking coating for pressure sensitive adhesives using cellulose

A yellow, hot melt alkyd traffic marking composition is described. The yellow, hot melt alkyd traffic marking composition contains 10-25 percent by weight of a hot melt alkyd binder, 5-10 percent by weight of a thermally stable 1,5- or 1,8-substituted anthraquinone colorant selected from a 1,5- or 1,8-substituted anthraquinone aromatic thioether and a 1,5- or 1,8-substituted anthraquinone aromatic thioether polyester, and 65-85 weight percent of a filler. The yellow, hot melt alkyd traffic marking composition of the invention may also contain other components used in traffic marking compositions, such as a reflectivity aid, a plasticizer, or an impact modifier. Other optional components are discussed below. The yellow, hot melt alkyd traffic marking compositions may be applied to any paved surface.

Yellow, hot melt alkyd traffic marking compositions

A yellow, hot melt adhesive traffic marking composition is described. The yellow, hot melt adhesive traffic marking composition contains 10-25 percent by weight of a hot melt adhesive binder, 5-10 percent by weight of a thermally stable 1,5- or 1,8-substituted anthraquinone colorant selected from a 1,5- or 1,8-substituted anthraquinone aromatic thioether and a 1,5- or 1,8-substituted anthraquinone aromatic thioether polyester, and 65-85 weight percent of a filler. The yellow, hot melt adhesive traffic marking composition of the invention may also contain other components used in traffic marking compositions, such as a reflectivity aid, a plasticizer, or an impact modifier. Other optional components are discussed below. The yellow, hot melt adhesive traffic marking compositions may be applied to any paved surface.

Yellow, hot melt adhesive traffic marking compositions

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Kingsport, TN, United States of America

Gary Robert Robe