Efficiency evaluation of the photocatalytic degradation of zinc oxide nanoparticles immobilized on modified zeolites in the removal of styrene vapor from air

Styrene monomer is a volatile organic compound that has many applications in plastics, rubber, and paint manufacturing industries. Exposure to styrene vapor has certain effects, including suppression of the central nervous system, loss of concentration, weakness and fatigue, and nausea and there is a possibility of carcinogenesis in long-term exposure. Therefore, it is necessary to control and eliminate this vapor. The aim of this study was to investigate the performance of zinc oxide nanoparticles on modified natural zeolites in removing styrene vapor from the air. Natural zeolites of clinoptilolite were modified using hydrochloric acid and diphenyldichlorosilane. Next, zinc oxide nanoparticles with different ratios of 3, 5, and 10 wt% were stabilized on the zeolites. To determine their characteristics, samples were used from BET, SEM and XRD analyses. The input styrene concentration and the ratio of nanoparticles stabilized on zeolites were studied as effective functional parameters on the removal process. The efficiency results of natural zeolites (Ze) and modified zeolites (Mze) in styrene adsorption from the air show that the styrene breakthrough in the bed of MZe compared to that of Ze increases approximately two times. Also, the results showed that the removal by the process of UV/MZe-ZnO 3%, UV/MZe-ZnO 5%, and UV/MZe-ZnO 10%, was 36.5%, 40%, and 26%, respectively. From the results it can be concluded that MZe can increase the efficiency of photocatalytic degradation. Clinoptilolites of Iran can be used as an adsorbent to remove polluted air in industries that have low concentrations and flow rates.     

Megasonic agitation for enhanced electrodeposition of copper

In this paper we propose an agitation method based on megasonic acoustic streaming to overcome the limitations in plating rate and uniformity of the metal deposits during the electroplating process. Megasonic agitation at a frequency of 1 MHz allows the reduction of the thickness of the Nernst diffusion layer to less than 600 nm. Two applications that demonstrate the benefits of megasonic acoustic streaming are presented: the formation of uniform ultra-fine pitch flip-chip bumps and the metallisation of high aspect ratio microvias. For the latter application, a multi-physics based numerical simulation is implemented to describe the hydrodynamics introduced by the acoustic waves as they travel inside the deep microvias.     

Enantiospecific Synthesis and Cytotoxicity Evaluation of Oximidine II Analogues

Analogues of the anticancer natural product oximidine II were prepared and evaluated for cytotoxicity. One analogue of oximidine II that carries a C15 allylic amide side chain as well as two analogues with C15 vinyl sulfone side chains were found to lack cytotoxicity against the cancer cell line SK‐Mel‐5, thereby confirming the necessity of the C15 enamide side chain of oximidine II for cytotoxicity. Four analogues, designed by comparative molecular similarity index analysis (CoMSIA), that feature a less complex macrolactone scaffold were prepared and tested. The two analogues carrying a C15 vinyl sulfone group and the two analogues with a C15 oximidine II enamide side chain showed weak cytotoxicity against the SK‐Mel‐5 cell line and other cell lines, indicating that the designed simplified macrocycles cannot replace the oximidine II macrocycle.     

Short fiber-reinforced oxide fiber composites

This paper presents a novel fiber spraying process for the manufacturing of short fiber bundle-reinforced Nextel™ 610/Al₂O₃-ZrO₂ oxide fiber composites (SF-OFC) and its characterization. First, the influence of varying fiber lengths (7, 14, and 28 mm, continuous fibers) and fiber orientations (unidirectional 0°, quasi-isotropic, ±45°) was investigated using hand-laid SF-OFC. Due to the weak matrix, the hand-laid material exhibited a strongly fiber-dominated material behavior, that is, variations in fiber length and orientation had a strong influence on the material properties. Second, the automated sprayed SF-OFC, however, exhibited a random orientation of the fiber bundles, which resulted in in-plane isotropic material properties. Average bending strengths of up to 177 MPa, strains of .39%, and a quasi-ductile fracture behavior were achieved. The strain was, therefore, in the range of fabric-reinforced OFC. While the bending strength of the SF-OFC was somewhat lower than that of fabric-reinforced OFC with the fiber orientation parallel to the loading direction, it was more than two times higher than the strength in 45° direction relative to the fabric reinforcement. Combined with good drapability and lower material costs compared to fabric-reinforced OFC, SF-OFC is, therefore, a promising material for industrial applications.     

Regenerated cellulose nanocomposites reinforced with exfoliated graphite nanosheets using BMIMCL ionic liquid

Green nanocomposites of regenerated cellulose/exfoliated graphite nanosheets films with low nanofiller loadings were prepared using environmentally benign 1-butyl-3-methylimidazolium chloride (BMIMCl) ionic liquid. X-ray diffraction revealed well developed intercalated nanocomposites. The tensile strength and Young's modulus of the prepared nanocomposites were increased by 97.5% and 172% respectively when 0.75 wt.% and 1 wt.% exfoliated graphite nanosheets were added. The results were validated using the Halpin–Tsai model. The exfoliated graphite nanosheets were unidirectionally aligned in the regenerated cellulose parallel to the surface of the nanocomposites as revealed by transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM). Also, the TEM and FESEM revealed uniform dispersion of the exfoliated graphite nanosheets and good interaction between the nanofillers and the matrix. The addition of the exfoliated graphite nanosheets enhanced the thermal stability and reduced the water absorption and diffusivity of the nanocomposites.     

Silica nanotubes and hollow silica nanofibers: Gas phase mineralization,polymerization catalysis and in-situ polyethylene nanocomposites

Gas phase mineralization and mesoscopic replication of polyvinyl alcohol (PVA) nanofibers represents an attractive route to the preparation of silica nanotubes and hollow fibers with independent control of pore diameter and wall size. In the sol/gel gas phase process, PVA nanofibers, produced by electrospinning of aqueous PVA, were encapsulated in a thin silica shell by repeated sequenced feed of SiCl₄ and H₂O vapors, followed by thermal degradation of the PVA core at 550 °C. The hollow fiber wall thickness was governed by the number of SiCl₄/H₂O cycles with an average increase of the wall size of 0.7 nm per cycle. In contrast to conventional sol/gel electrospinning and wet sol/gel dip coating, shearing of such hollow silicate nanofibers afforded single silica nanotubes with an average length of a few microns. Aqueous silica sols added together with PVA gave control of the inner pore architectures. Methylalumoxane (MAO) activated silica nanotubes were used as supports for half sandwich chromium (III) (Cr) and post metallocene (Fe) catalysts for ethylene polymerization and in-situ nanocomposite formation with uniform dispersion of silica nanotubes within the polyethylene matrix. A blend of Cr and Fe was supported on silica nanotubes to produce melt processable polyethylene nanocomposites with bimodal molecular weight distributions.