Thermoplastic Polyurethane with a Percisely Controlled Biodegradation Rate

Title: PROCESS FOR MAKING BIODEGRADABLE AND/OR BIOABSORBABLE POLYMERS

 Number/Link: WO2014/004334

Applicant/Assignee: Lubrizol

Publication date: 03-01-2014

Gist”: Two sets of parameters are given (and claimed) which, when iteratively adjusted, allow to independently modify the mechanical properties and biodegradation rate of a TPU.

Why it is interesting: Many biomedical materials for implants such as screws, bone plates, tissue scaffolds, pins etc need high mechanical properties but also a controlled biodegradation rate which can vary from weeks to years.  According to this case the precise control of the degradation rate is not possible with currently available bio-polymers.  The invention claims two sets of parameters one which controls the physical properties of a TPU like the molecular weight, harblock content, crystallinity etc, and another set which controls the biodegradation rate like the amount of ‘hydrolyzable units’ in the backbone, hydrophilicity ect. It is claimed that both mechanical properties and degradation rate can be independently controlled by adjusting one or more parameters of each set. In the examples TPUs are prepared from HMDI, 1,4-butane diol and poly(lactide-co-caprolactone) diols where the lactide is the hydrolyzable unit.

A poly(lactide-co-caprolactone)

A poly(lactide-co-caprolactone)

Thermoplastic Polyurea Elastomers

Title: MELT PROCESSIBLE POLYUREAS AND POLYUREA-URETHANES, METHOD FOR THE PRODUCTION THEREOF AND PRODUCTS MADE THEREFROM

 Number/Link: US2013/0331538

Applicant/Assignee: University of Akron

Publication date: 12-12-2013 (priority PCT)

Gist”: Polyurea is made melt-processable by incorporating hydrogen-bond accepting chain extenders (HACE)

Why it is interesting: It is well known that polyurea elastomers with a decent hardblock content (of e.g. 30-35%) are not melt-processable. Because of very strong (bi-dentate) H-bond formation in the hard domains the material will degrade sooner than flow when heated. In this invention it is proposed to incorporate a relatively small amount of HACE to disrupt the hard domain structure and reduce flow temperature.  In an example a few parts of OH-ended pentamethylenepolycarbonate with a MW of 500 to 800 was used next to the conventional 1,6-hexamethylene chain extender to drop the flow temperature by 50°C while not affecting the tensile strength. (I suppose a NH2-ended polycarbonate could have been used as well to make an all-polyurea material).

Bi-dentate H-bonds between polurea molecules (left) disrupted by a polycarbonate group (right)

Bi-dentate H-bonds between polurea molecules (left) dusrupted by a carbonate group (right)

Toughened Thermoplastic Polyurethane

Title: Method Of Toughening Thermoplastic Polyurethane And Articles Comprising Toughened Thermoplastic Polyurethane

 Number/Link: US2013/0323512

Applicant/Assignee: Nike

Publication date: 5-12-2013

Gist”: TPU is interpenetrated with a thermosetting PU using a solvent

Why it is interesting: According to this invention a conventional TPU can be “toughened” by dipping and  swelling it in a solution containing (about) 20% of a PU-forming composition comprising a polyester polyol, a chain extender, a mixture of pure and polymeric MDI and DBTDL as a catalyst.  The solvent is preferably acetone. The swollen TPU is dried and the PU is cured by heating. It is believed that a TPU-PU interpenetrating polymer network (IPN) is formed.  The invention is targeted at improving the scuff resistance of golf balls. (scuff resistance=resistance against failure of the coating by shear stress).

Nike golf ball.

Nike golf ball.

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