Triptycene Chain Extenders

Title: TRIPTYCENE MONOMER AND TRIPTYCENE CONTAINING POLYESTERS AND POLYURETHANES

 Number/Link: US20150191408

Applicant/Assignee: not yet recorded. Research supported by US Army

Publication date: 9-07-2015

Gist”: A novel primary diol derived from triptycene is useful as chain extender for polyurethanes and polyesters.

Why it is interesting: Polymers with increased mechanical properties and stiffness can be obtained by incorporating rigid structures in the polymer chain.  This however also results in increased glass transition temperature and reduced ductility because of reduced chain flexiblity and entanglements.  According to this invention polyurethanes (and copolyesters) with high modulus and good ductility at low temperatures can obtained by using triptycene-1,4-hydroquinone-bis(2-hydroxyethyl ether) or TD. In and example TD capped with PEG400 is reacted with a 4,4’MDI- PTMEG1000 prepolymer.  The resulting material indeed has a very low softblock Tg of  -65ºC and a much higher Y modulus compared to a PU made with HQEE as chain extender. According to the inventors the PU is highly suitable as a matrix material in KEVLAR or UHMWPE fiber composites.
In my opinion this is a very interesting chain extender as it appears to prevent H-bond formation and increase molar volume thereby substantially decreasing Tg. However lack of availability, and (most probably) price, will prevent this from becoming mainstream anytime soon.

Tryptycene-1,4-hydroquinone-bis(2-hydroxyethyl ether)

Triptycene-1,4-hydroquinone-bis(2-hydroxyethyl ether)

 

Polyurethanes with Reduced Aldehyde Emissions

Title: POLYURETHANES HAVING REDUCED ALDEHYDE EMISSION

 Number/Link:WO2015/082316 (German)

Applicant/Assignee: BASF

Publication date: 11-06-2015

Gist”: Use of CH-acidic compounds as aldehyde scavengers

Why it is interesting: Reducing VOC emissions, and especially aldehyde emissions, from polyurethane systems remains an important research topic and has been discussed before on this blog (see e.g.  here and here). To reduce aldehyde emissions, scavenger molecules are used which are often amines or hydrazine compounds.  In this invention however the aldehyde scavenger is a CH-acidic compound of the form R-CH2-R’ in which R and R’ are electron-withdrawing groups. The R-groups can be iso-reactive and the molecule can (preferably) contain more than one acidic CH2 group, like e.g. trimethylolpropane triacetoacetate. Other examples are N,N-dimethylacetoacetamide and dimethyl 1,3-acetonedicarboxylate. The compounds are used in an amount of 0.5 to 1 pphp, are said to have advantages over the prior art like less or no catalytic activity and do not lead to extra emissions.

Trimethylolpropane triacetoacetate

Trimethylolpropane triacetoacetate

Polyols from Epoxies and Cardanol

Title: CARDANOL MODIFIED EPOXY POLYOL

 Number/Link: WO2015/077944  WO2015/077945 WO2015/078178

Applicant/Assignee: Dow

Publication date: 4-06-2015

Gist”: Polyols are prepared by reacting an epoxy resin with  cashew nutshell liquid.

Why it is interesting: Cardanol is the main component of  cashew nutshell liquid which is a by-product of cashew nut processing. It is a “surfactant-like” phenolic compound which, when reacted with a polyepoxide, will result in a polyol with sec-OH groups. When used in polyurethane formulations these polyols will (unsurprisingly) be slow-reacting, highly hydrophobic and show compatibilizing properties vs apolar compounds. Dow have therefore filed three patent applications on PU systems containing these polyols: one on slowly-reacting PU systems for filament winding, one on highly hydrophobic PU elastomers and one on asphalt-PU compositions.
These are interesting polyols but they could be hard to process in my opinion.

Cardanol is reacted with bisphenol-A diglycidylether resulting in a diol according to the invention

Cardanol is reacted with bisphenol-A diglycidylether resulting in a diol according to the invention

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