Fatigue life enhancement by irradiation of 12Cr1MoV steel with a Zr<Superscript>+</Superscript> ion beam. Mesoscale deformation and fracture

The structure and properties of 12Cr1MoV steel irradiated with a zirconium ion beam were studied by optical microscopy, scanning electron microscopy, and micro- and nanoindentation. It is shown that the modification covers the entire cross-section of the irradiated specimens to a depth of 1 mm. The data on irradiation-induced structural changes are used to interpret the changes in mechanical properties of the irradiated specimens under static and cyclic loading. Particular attention is given to analysis of strain estimation by the digital image correlation method.     

Use of circular variance to quantify the deviation of a macromolecule from the spherical shape

It is shown that the extent of deviation of a molecular shape from spherical can be characterized by comparing the distribution of the circular variances, a measure originally proposed to quantify angular spread, of the vectors from each atom to the rest of the molecule to the circular variance of a collection of atoms filling the unit sphere. Different measures for quantifying the difference between distribution are proposed and compared.     

Imprisoned lightning: charge transport in trehalose-derived sugar glasses

Trehalose is a naturally occurring disaccharide noted for its ability to preserve the biological function of proteins and cell membranes during periods of stress—such as water deprivation or extreme temperature—by stabilizing the conformations of the macromolecules within a glassy matrix. This phenomenon makes use of the propensity for trehalose to interact strongly with protein functional groups and solvent water molecules via hydrogen bonding. Previously, it has been shown that trehalose sugar glasses also support long-range charge transport in oxidation-reduction reactions occurring between spatially separated donors and acceptors. Here, through the use of bulk Arrhenius DC-conductivity measurements, we infer that this anomalously high carrier mobility is due to proton hopping along a hydrogen bonding network formed by sorbed “water wires,” a process known as the Grotthuss mechanism. Additionally, we find that the apparent activation energy of the conductivity depends non-monotonically on the bias voltage. The possibility is raised for novel photovoltaic devices based on the entrapment of photosynthetic proteins within these glasses.     

Malononitrile-involved Michael addition polymerization: An efficient and facile route for cyano-rich polyesters with programmable thermal and mechanical properties

An efficient, atom-economic, oxygen-tolerant, and water-tolerant strategy has been established to synthesize cyano-rich polyesters. Four kinds of organic bases, 1,1,3,3-tetramethylguanidine (TMG), 4-dimethylaminopyridine, triethylamine, and 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) were explored for accelerating Michael addition polymerization of malononitrile and 1,4-butandiol diacrylate. TMG can promote the polymerization efficiently under mild conditions to quantitatively afford polyester with high-molecular weight and moderate polydispersity. The comparison of the kinetic studies of TMG and TBD reveals that TMG shows better catalytic performance, while the catalysis of TBD brings about oligomers in spite of the higher efficiency at early age of the polymerization. Moreover, other diacrylate compounds could also be quantitatively polymerized to afford polyesters with high molecular weight. When dimethacrylate is chose as the monomer, the polymerization becomes sluggish. All the afforded polyesters display programmable thermal and mechanical properties that are closely related to their chemical structures.