Polyester Polyol with PDMS Backbone

Title: POLYESTER POLYOL, POLYURETHANE OBTAINED USING THE SAME, PROCESS FOR PRODUCTION THEREOF, AND MOLDED POLYURETHANE

 Number/Link: US2014/0246621

Applicant/Assignee: Mitsubishi Chemical

Publication date: 4-09-2014 (priority PCT)

Gist”: A polyester polyol is prepared from a caboxylic acid-modified PDMS and a polyether diol.

Why it is interesting: A polyester polyol is prepared form a linear polydimethylsiloxane end-capped with carboxylic acid groups and having a molecular weight between about 500 and 4000 together with a polytetramethyleneether glycol with MW of 500 to 2000, such that the PDMS content is about 40% . The use of this polyol in polyurethane elastomers results in modified surface characteristics like reduced tackiness. The invention mentions fibers and films as potential applications, but this could be an interesting polyol for many other applications as well. Interesting idea but probably not new.  Only one claim appears to have survived the filing process.

 

Representation of the polyester polyol according to the invention

Representation of the polyester polyol according to the invention

Isocyanate-Free Polyurethanes Using Azide-Alkyne Click Chemistry

Title: SYNTHESIS OF POLYURETHANE POLYMERS VIA COPPER AZIDE-ALKYNE CLICK CHEMISTRY FOR COATINGS, ADHESIVES, SEALANTS AND ELASTOMER APPLICATIONS

 Number/Link: WO2014/122153

Applicant/Assignee: Sika

Publication date: 14-08-2014

Gist”: Polyurethane prepolymers capped with azides and alkynes are reacted using copper catalysis.

Why it is interesting: Because of safety, health and envriromental issues, isocyanate-free systems have clearly been gaining in importance the last few years.  Especially for coatings, adhesives and OCF applications, alternative curings systems are being developed. In the current invention an isocyanate-free system is based on the reaction between a prepolymer having at least two azide groups and a prepolymer having at least two alkyne groups. The reaction is copper catalyzed such that it can be performed at ambient temperature. The first prepolymer is (pref.)  prepared by reacting an isocyanate ended prepolymer with glycidol (2,3-epoxy-1-propanol) and subsequently with sodium azide. The second prepolymer is similarly prepared by reacting an isocyanate ended prepolymer with propargyl alcohol (2-propyn-1-ol).  The systems are said to be especially useful for roof coatings.

Example of an azide-alkyne reaction resulting in 1,4-disubstituded triazoles.

Example of an azide-alkyne reaction resulting in 1,4-disubstituded triazoles.

 

Polyurethane Dispersions with “Reversible Drying”

Title: RADIATION CURABLE AQUEOUS COMPOSITIONS WITH REVERSIBLE DRYING

 Number/Link: WO2014/111349

Applicant/Assignee: Allnex

Publication date: 24-07-2014

Gist”: PUDs from hydrophilic, low molecular weight PU can be re-dispersed after drying.

Why it is interesting: It is known that PUDs will coalesce into an insoluble film when dried, at least when the temperature is over the ‘minimum film forming temperature’ or MMFT.  This behaviour, while being useful in most coating- and adhesives applications, can be problematic when the PUDs are used for jet-printing inks because of irreverisble blocking of the print-head nozzles.  According to this invention re-dispersible PUDs can be made when the PU used is both sufficiently hydrophilic and of a low average molecular weight (pref. an Mn between 1000 and 5000, with a polydispersity between 2 and 4). The PU does need to be radiation curable so it can be crosslinked after drying.  In the examples a low NCO prepolymer is prepared from 1,6-hexanediisocyanate (HDI), 2,2-dimethylolpropionic acid, some polyester or polycarbonate polyol and an acrylic chainstopper like a propoxylated trimethylolpropane diacrylate. The (viscous) prepolymer is dispersed and neutralized by adding water containing NaOH or triethylamine. After drying the PUDs of the invention can be re-dispersed in water at 25°C.

Film-forming PU dispersion.

Film-forming PU dispersion.

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