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)

Sulfur Containing Polyurethane Elastomers for Tires and “Tweels”

Title: Polyurethane

 Number/Link: US2013/0287982

Applicant/Assignee: Michelin

Publication date: 31-10-2013  (priority PCT/FR)

Gist”: Use of dithiodiols or dithiodiamines in polyurethane elastomer formulations for improved adhesion to metal.

Why it is interesting: The current invention relates to polyurethane elastomers containing a chain extender mixture consisting of a conventional chain extender (e.g. butandiol) and 1-30% (of the total chain extender) of an S-S bridge containing diol or diamine like 2,2′-dithiodiethanol or 4,4′-dithiodianiline. The resulting polyurethane reportedly shows an increased bonding strength  to metal, which can be even more enhanced by adding elemental sulfur and conventional sulfur-containing rubber-curing accelerators like dithiocarbamates, thiurams, thiazoles etc. (as well known in the art of rubber vulcanization). The resulting polyurethanes are useful for the production of metal strand-reinforced composites like tires and ‘tweels’ (tweel=tire+wheel  see http://michelintweel.com/index.html).

Michelin "tweel"

Michelin “tweel”

Very Tough Polyurethane Elastomers Based on a Novel Type of Polyester Polyol

Title: POLYESTER POLYOL FOR USE IN POLYURETHANE

 Number/Link: WO2013/156450

Applicant/Assignee: Purac Biochem

Publication date: 24-10-2013

Gist”: Tough polyurethane elastomers can be prepared from polyester polyols based on dimer acid and lactide oligomers.

Why it is interesting: The invention claims a new type of ABA polyester polyol where A is a hydrophilic lactide oligomer and B is a hydrophobic dimer diacid initiator. The lactide ologimers can be produced by ring-opening polymerization of cyclic lactide and preferably contain between 4 and 16 lactoyl units.  The dimer diacid is prepared by dimerizing unsaturated C12 to C22 fatty acids, preferably linoleic or linolenic acid. The molecular weight of the polyester polyol is preferably between 1000 and 3500 dalton. Solid polyurethane elastomers prepared from this type of polyols reportedly have much improved toughness and other mechanical properties.

Example of a Dimer Acid

Example of a Dimer Acid

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