Thermoplastic polyurethanes (PUs) can display shape-memory (SM) characteristics if their microphase-separated structure, consisting of domains formed by hard blocks and soft segments, respectively, is complemented with the ability of the soft segments to partially crystallize, so that the third phase thus formed can serve as the switching element for the shapememory effect. While property modifications of SMPUs usually require de novo synthesis, we show at the example of a commercially available poly(ester urethane) consisting of crystallizable poly(1,4-butylene adipate) soft/switching segments and hard segments composed of 4,4methylenediphenyl diisocyanate and 1,4-butanediol that the thermomechanical properties can also be modified by formulating nanocomposites and/or influencing the crystallization of the soft/switching segments via the addition of a nucleating agent. The incorporation of cellulose nanocrystals (CNCs) by simple melt-mixing allowed increasing the tensile storage modulus from 150 MPa (neat polymer) to 572 MPa (15% w/w CNCs) while the shape fixity at a specific fixing temperature was increased from 47 to 75%. The temperature at which good fixity (>97%) could be rapidly achieved was increased from 10 to 25ºC upon addition of 1% w/w dodecanoic acid, which served to nucleate the poly(1,4-butylene adipate) crystallization.
A note on versions:The version presented here may differ from the published version or from the version of record. If you wish to cite this item you are advised to consult the publisher's version. Please see the repository url above for details on accessing the published version and note that access may require a subscription.For more information, please contact eprints@nottingham.ac.uk J o u r n a l Na me A theory of dynamic nuclear polarisation (DNP) by thermal mixing is suggested based on purely quantum considerations. A minimal 6-level microscopic model is developed to test the theory and link it to the well-known thermodynamic model. Optimal conditions for the nuclear polarization enhancement and effects of inhomogeneous broadening of the electron resonance are discussed. Macroscopic simulations of nuclear polarization spectra displaying good agreement with experiments, involving BDPA and trityl free radicals, are presented.
A combined electrochemical and theoretical study suggests that hydrogen evolution from weak acids catalyzed by a structural mimic of the active site of NiFe hydrogenases [Ni(xbsms)Ru(C6Me6)Cl](+) proceeds through proton-coupled electron transfer steps.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.