Transfer of angular momentum to matter from acoustical vortices in free space

An experimental demonstration of the mechanical transfer of orbital angular momentum to matter from acoustical vortices in free field is presented. Vortices with topological charges l=+/-1 and l=+/-2 were generated and a torsion pendulum was used to study the angular momentum transfer to hanging disks of several sizes. This allowed us to make a comparative study of the effective acoustical torque in terms of topological charge of the vortex, the disk radius, and its position along the main propagation axis. A theoretical discussion of the generated sound fields is also provided.     

Weak and strong hydrogen bonds conducting the supramolecular framework of 1-butyl-3-(1-naphthoyl)thiourea: crystal structure,vibrational studies,DFT methods,Pixel energies and Hirshfeld surface analysis

A detailed structural and spectroscopic study of a new thiourea derivative 1-butyl-3-(1-naphthoyl)thiourea (1) is presented with the assistance of theoretical calculations. The X-ray diffraction structure analysis reveals a planar carbonylthiourea group, favoured by intra-molecular NH···O bond. The compound is arranged in the lattice as NH···O and NH···S bonded polymeric ribbons, that extend along the crystal b-axis. Molecular pairs involving N–H···S hydrogen bonds are a dominant contribution to packing stabilisation coming from coulombic component. Hirshfeld surfaces and two-dimensional-fingerprint plots show different intermolecular contacts and its relative contributions to total surface in each compound. The AIM approach shows the nature and strength of the strong and weak intramolecular interactions and the solvent effect, while NBO analysis reveals that the sulphur atom is responsible for the higher hyperconjugative stabilising energy.     

PLA and PBAT-Based Electrospun Fibers Functionalized with Antibacterial Bio-Based Polymers

Antimicrobial fibers based on biodegradable polymers, poly(lactic acid) (PLA), and poly(butylene adipate-co-terephthalate) (PBAT) are prepared by electrospinning. For this purpose, a biodegradable/bio-based polyitaconate containing azoles groups (PTTI) is incorporated at 10 wt.% into the electrospinning formulations. The resulting fibers functionalized with azole moieties are uniform and free of beads. Then, the accessible azole groups are subjected to N-alkylation, treatment that provides cationic azolium groups with antibacterial activity at the surface of fibers. The positive charge density, roughness, and wettability of the cationic fibers are evaluated and compared with flat films. It is confirmed that these parameters exert an important effect on the antimicrobial properties, as well as the length of the alkylating agent and the hydrophobicity of the matrix. The quaternized PLA/PTTI fibers exhibit the highest efficiency against the tested bacteria, yielding a 4-Log reduction against S. aureus and 1.7-Log against MRSA. Then, biocompatibility and bioactivity of the fibers are evaluated in terms of adhesion, morphology and viability of fibroblasts. The results show no cytotoxic effect of the samples, however, a cytostatic effect is appreciated, which is ascribed to the strong electrostatic interactions between the positive charge at the fiber surface and the negative charge of the cell membranes.     

Polymerization and copolymerization of styrene by Ph2Zn‐metallocene‐MAO initiator systems.

Combined systems including diphenylzinc, Ph₂Zn, a metallocene, and methylaluminoxane, MAO, have been employed to initiate styrene polymerization. These initiator systems have been also used to initiate the copolymerization of styrene with p‐alkylsubstituted styrenes and with α‐olefins. Both polymerization and copolymerization processes depend on the nature of the metallocene included in the initiator system, the presence of Ph₂Zn, the temperature and the solvent used. Titanocenes produced syndiotactic polystyrene, s‐PS, while zirconocenes gave atactic polystyrene, a‐PS, with a certain content, less the 20% of s‐PS. For copolymerizations the conversion to polymer was also influenced by the comonomer nature and its molar proportion in the initial feed, as well as the sort of metallocene, titanocene or zirconocene included.