Isocyanate-based laminating adhesives

Stock material or miscellaneous articles – Composite – Of polyamidoester

Reexamination Certificate

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C156S331400, C156S331700, C206S813000, C428S425100, C428S425800, C428S423500, C428S423700, C428S424200, C428S424400, C428S424600, C428S424800, C428S311710, C428S319300, C528S066000, C528S076000, C528S080000, C528S083000, C528S905000

Reexamination Certificate

active

06617031

ABSTRACT:

FIELD OF THE INVENTION
The invention relates to solventless laminating adhesives, specifically to isocyanate-based formulations having enhanced processing characteristics at reduced temperatures.
BACKGROUND OF THE INVENTION
It is known that isocyanate-based formulations are useful laminating adhesives for flexible packaging. The solventless formulations, which consist of a polyol (part A) and an NCO-terminated polyurethane prepolymer (part B), are meter-mixed immediately before the laminating process and used to adhere superposed layers of one or more materials. For example, European Patent Application #93114668.2 discloses such formulations wherein the part A and part B components are meter-mixed at temperatures between 20° C. and 50° C.
A drawback in this prior art reference is the formulation's initial viscosity. The formulations, which have initial viscosities greater than 25,000 mPa·s at 25° C.+/−5.0° C., are difficult to process.
Therefore, there remains a need for solventless isocyanate-based laminating adhesives having enhanced processing characteristics at reduced temperatures.
SUMMARY OF THE INVENTION
The present invention is directed to solventless isocyanate-based formulations, which are useful as laminating adhesives for flexible packaging, comprising the reaction product of:
A) at least one polymeric polyol (part A) comprising;
1) at least one alkylene diol;
2) at least one diol containing a pendant aliphatic chain;
3) at least one dicarboxylic acid; with
B) at least one NCO-terminated polyurethane prepolymer (part B) comprising;
1) at least one polymeric polyol; and
2) at least one polyisocyanate.
The part A components which have viscosities less than about 12,000 mPa·s at 25° C.+/−5.0° C. improve the meter-mix process, through enhanced flow rates, without the addition of heat.
Surprisingly, the formulations of the present invention have initial viscosities less than about 25,000 mPa·s at 25° C.+/−5.0° C. These properties enhance safety and simplify processing on conventional meter-mix units. For example, combining the part A and part B components without additional heat reduces worker exposure hazards to volatile isocyanates present in the part B component. Although distillation methods can reduce the volatile isocyanates present in the part B component to less than about 0.1% by weight, the small quantities which remain can still generate safety hazards when heated.
The present invention further comprises a method wherein the adhesive formulations are processed on laminator units at temperatures of about 75° C. and line speeds from about 200 meters/min. to about 500 meters/min. Lower temperatures are preferred during the solventless laminating process. For example, elevated temperatures accelerate the isocyanate/hydroxyl reaction to generate viscous materials. Viscous materials tend to mist on solventless laminators which are run at high line speeds. Misting is a phenomenon wherein adhesive droplets are thrown into the air generating safety hazards and non-uniform coat weights. The inventive formulations can be processed, on solventless laminators without misting, at temperatures of less than about 75° C. and line speeds from about 200 meters/min. to about 500 meters/min.
The adhesive formulations have good adhesion characteristics on substrates such as wood, metal, plastic and synthetic polymers. Examples include paper, polyethylene, polypropylene, polyester, nylon, wood, ethylene vinyl acetate, cellophane, polyvinyl chloride, surlyn, aluminum and metallized films.
Said formulations are particularly useful film to film laminating adhesives in durable-goods applications and applications having indirect food contact.
DETAILED DESCRIPTION OF THE INVENTION
At least one low molecular weight alkylene diol is used in the preparation of the part A component. The alkylene diols have hydroxyl numbers, as determined by ASTM designation E-222-67 (Method B), in a range from about 130 to about 1250, and preferably from about 950 to about 1250. Suitable examples include ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, 1,4-bis-(hydroxymethyl)-cyclohexane, furan dimethylol, and mixtures thereof. Preferred alkylene diols are 1,4-butanediol, 1,6-hexanediol and mixtures thereof. The diols are present in a range from about 5.0% by weight to about 25.0% by weight, and preferably from about 10.0% by weight to about 20.0% by weight, based on 100 parts total part A solids.
Low molecular weight polyols containing alkoxy groups may be used in the preparation of the part A component. Suitable examples include diethylene glycol, polyethylene ether glycol, polypropylene ether glycols, polytetramethylene ether glycols and their mixtures. The polyols can have hydroxyl numbers in a range from about 130 to about 1250, and preferably from about 950 to about 1250 and can be present in the part A component in a range from about 5.0% by weight to about 50.0% by weight, and preferably from about 10.0% by weight to about 40.0% by weight, based on 100 parts total part A solids.
A least one low molecular weight diol component containing a pendant aliphatic chain are used in the preparation of the part A component. The term “pendant” is defined as a hydrophobic group which extends from the polymer chain. The diols can have hydroxyl numbers in a range from about 130 to about 1250, and preferably from about 950 to about 1250. Examples include 1,2-propanediol, 1,2-butanediol, 1,3-butanediol and 2,3-butanediol, 2,2-methyl-1,3-propanediol, 2,2,4-trimethyl-1,3-pentanediol, neopentyl glycol, 2-butyl-2-ethyl-1,3-propanediol and bis-2-hydroxyethyl lauramide and 1,2-dodecanediol. The diols can be present in the part A component in a range from about 5.0% by weight to about 50.0% by weight, and preferably from about 10.0% by weight to about 40.0% by weight, based on 100 parts total part A solids. It is surmised that some of the adhesive formulations' unique properties can be attributed to the pendant aliphatic chains present in the part A component.
Higher functional polyols may be used in the preparation of the part A component. Suitable examples include glycerol, trimethylolpropane, 1,2,4-butane triol, 2,6-hexane triol and mixtures thereof. The preferred higher functional polyols are glycerol and trimethylolpropane. Said polyols may be present in a range from about 1.0% by weight to about 15.0% by weight, and preferably from about 5.0% by weight to about 10.0% by weight, based on 100 parts total part A solids.
At least one polycarboxylic acid component is used in the preparation of the part A component. The polycarboxylic acid may be aliphatic, cycloaliphatic, aromatic and mixtures thereof. Suitable examples include oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, maleic acid, fumaric acid, phthalic acid, isophthalic acid, terphthalic acid, diethyl succinic acid and 1,4-cyclohexane dicarboxylic acid. The preferred polycarboxylic acid components are adipic acid, isophthalic acid and mixtures thereof. The polycarboxylic acids can be present in the part A component in a range from about 50.0% by weight to about 85.0% by weight, and preferably from about 50.0% by weight to about 70.0% by weight, based on 100 parts total part A solids.
The resulting polymeric polyols, which are the condensates of said polyhydroxyl and polycarboxylic acid components previously described, have viscosities less than about 12,000 mPa·s at 25° C. Suitable available polymeric polyols include Rucoflex® XF-5604-210 which is a polyester polyol from Ruco Corporation (Hicksville, N.Y.) based on adipic acid, isophthalic acid, glycerol, 1,6-hexanediol and neopentyl glycol. It is surmised that multibranched polymeric polyols (i.e., aliphatic pendant chains) reduce the crystalline nature of the part A component enhancing its flow characteristics at reduced temperatures. The effects of chain branching on polymer viscosity is described in “Polymer Process Engineering”, Eric A.

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