Highly Tuneable Shape Memory Polyurethanes

Patent Title: PROCESSABLE, TUNABLE THIOL-ENE CROSSLINKED POLYURETHANE SHAPE MEMORY POLYMERS

 Number/Link: WO2016/126703

Applicant/Assignee: Texas A&M University

Publication date: 11-08-2016

Gist”: SMPUs are made from combinations of different diisocyanates and chain extenders and different levels of crosslinking using thiol-ene click chemistry

Why it is interesting: This invention is about shape memory polyurethanes with tuneable glass transition temperature and stiffness. In a first step a low mole weight TPU is prepared from a diisocyanate and a short chain diol including some trimethylolpropane allyether (TMPAE) and allylalcohol as chain stopper. The TPU is then blended with a polythiol and a photoinitiator to allow for UV curing. The Tg can be tuned from 30 and 105°C by combining different types of chain extenders and di-iso’s ranging from DEG-HDI to CHDM-H12MDI.  The modulus (in the rubber state) can be  varied between 0.4 to 20 MPa by controlling the level of crosslinking through the amount of TMPAE and amount and type of polythiol.  The SMPUs are said to be especially useful for biomedical applications.

Reaction scheme of the invention

Reaction scheme of the invention

Polyurethanes from Mevalonolactone

Patent Title: POLYMERS PREPARED FROM MEVALONOLACTONE AND DERIVATIVES

 Number/Link: US2016/0130389

Applicant/Assignee: Visolis

Publication date: 12-05-2016

Gist”: Use of mevalonolactone derivatives as monomers for PU and other polymers

Why it is interesting: 3,5-Dihydroxy-3-methylvaleric acid and its corresponding lactone “mevalonolactone”, is a common metabolic intermediate and can be produced industrially by fermentation of biomass. Mevalonolactone can be converted to diacids, (unsaturated) diols, triols etc., which could be useful as a renewable and inexpensive feedstock for polymers like polyester, polyamides and polyurethanes. In an example mevalonolactone is reacted with ethanolamine resulting in the triol  3,5-dihydroxy-N-(2-hydroxyethyl)-3-methylpentanamide which is in turn reacted with 4,4′ MDI to make a model polyurethane.

Dihydroxymethylvaleric acid and its corresponding lactone

Dihydroxymethylvaleric acid and its corresponding lactone

Thermoreversible Polyurea

Patent Title: DYNAMIC UREA BONDS FOR POLYMERS

 Number/Link: W02016/069582

Applicant/Assignee: University of Illinois

Publication date: 6-05-2016

Gist”: Urea bonds prepared from sterically hindered amines and isocyanates

Why it is interesting: The N-C bond in urea is very stable due to conjugation of the lone electron pair of the nitrogen atom with the cabonyl group.  According to this invention, the nitrogen atom can be subsituted with a strongly hindering group such that the coplanarity, and therefore most of the conjugation, of the C-N and C=O bonds is lost. These hindered urea bonds are much less stable and can reversibly depolymerize at relatively low temperatures. Thermoreversible bonds can be useful in a number of smart materials such as self-healing-, “4D printing”- , and reprogrammable shape memory materials. In an example a shape memory material with a Tg of 53°C and a Young’s Modulus of about 2 GPa was prepared by reacting 2-(t-buylamino)ethanol (TBAE) and trimerized hexamethylene diisocyanate (THDI). The ‘permanent shape’ of the material could be re-programmed by forcing the material in a new shape for 72 hours at 60°C.

Polurethane-urea with thermoreverisble urea bonds

Poly(urethane-urea) with thermoreverisble urea bonds

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