Polyurethane Tissue Adhesives

Patent Title: URETHANE DECOMPOSING METHOD AND URETHANE DECOMPOSING AGENT

 Number/Link:  US2016/0257800

Applicant/Assignee: Obihiro University

Publication date: 8-09-2016 (priority PCT/JP)

Gist”: Prepolymer from ether-ester polyol and aliphatic isocyanate

Why it is interesting: There is a growing trend in current surgerical practice to replace sutures and staples with adhesives. These tissue adhesives need to have a particular set of properties, like the correct viscosity, hardening speed, biodegradability and toxic and allergenic properties. Current surgical adhesives are often cyanoacrylates, which react very fast, are brittle and show poor biodegradability, or protein-based adhesives which are costly and form weak bonds. According to this invention an improved polyurethane tissue adhesive can be prepared from an isocyanate-ended prepolymer based on an aliphatic isocyanate and a polyol.  The polyol is prepared from a starter polyol or amine which is reacted with a mixture of an alkoxide and about 10-20% of a  lactide (or glycolide or cyclic acid anhydride).  The lactide is randomly copolymerized with the alkoxide using DMC catalysis. The polyol is then reacted with an aliphatic isocyanate, pref. HDI or IPDI in a NCO/OH ratio of about 8:1. After that monomeric isocyanate is removed by thin film distillation down to less than 1% free monomer.
The adhesives are said to be fast, non-toxic, non-allergenic and biodegradable.

L-Lactide

L-Lactide

Self-Crosslinkable Polyurethane

Patent Title: Self-Crosslinkable Polymer and Aqueous Dispersion Comprising Particles of the Same

 Number/Link: US2016/0159959

Applicant/Assignee: Valspar Sourcing

Publication date: 9-06-2016

Gist”: Aqueous dispersion of polyurethane having both azide and carbonyl groups in the backbone

Why it is interesting: Properties of water-based PU coatings can often be improved by incorporating olefinically unsaturated groups in the polymer which can be crosslinked using radiation. According to this invention a self-crosslinking (i.e. without the need for radiation) aqueous PU coating composition can be made by incorporating both azide- and carbonyl groups into the PU backbone. When the water evaporates and the film forms these groups will react forming a hydrazone-type bond. The self-crosslinkabe polymer can be prepared by first making an NCO-ended prepolymer containing a reactive double bond, by (e.g.) reacting some of the NCO groups with hydroxyethylmethacrylate (HEMA). This prepolymer is then dispersed in water together with hydrazine and and acrylate like MMA or BA. The hydrazine will react with the NCO groups, introducing azide groups into the backbone.  The acrylate and the prepolymer are then suspension polymerized using an initiator.  The PU backbone can (optionally) contain a water dispersible group – e.g. by incorporating dimethylolpropanoic acid. The self-crosslinkable polymer is said to be especially useful for use in wood coating compositions.

Hydrazine

Hydrazine

 

Polyurethane-Epoxy IPN Composites

Patent Title: POLYMER COMPOSITE THERMAL INTERFACE MATERIAL WITH HIGH THERMAL CONDUCTIVITY

 Number/Link: WO2016/079627

Applicant/Assignee: IBM

Publication date: 26-05-2016

Gist”: PU-Epoxy IPN particle composites show improved thermal conductivity

Why it is interesting: The application is about thermally conductive adhesives for use with electronic components. Commonly these materials consist of polymers filled with thermally- (but not electrically-) conductive particles such as AlN, BN and ZnO. According to the invention the thermal conductivity of these composites can be improved by using a polyurethane-epoxy true interpenetrating polymer network (IPN) as the matrix. In the examples a MDI-polycaprolactone prepolymer is mixed with a BPA diglycidylether prepolymer and boron nitride (BN) particles and crosslinked using trimethylolpropane and imidazole.  The thermal conductivity of the composite shows a synergy, meaning that it is clearly higher than the conductivities of both the PU or EP composites. The synergy is said to be due to an enhanced distribution of the BN particles and (because this is IBM and they are very clever) due to enhanced phonon scattering.

Bisphenol-A diglycidylether

Bisphenol-A diglycidylether

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