A nanoparticle-based drug delivery system is first established by mesoporous silica encapsulating amino acid–intercalated layered double hydroxide (LDH) to construct nanocomposites AA-LDH@MS. The amino acids including phenylalanine (Phe) and histidine (His) with aromatic groups are intercalated into LDH as the cores Phe-LDH and His-LDH. These nanocomposites AA-LDH@MS display multispaces of the interlayer spaces of LDH and porous channels of mesoporous silica to load drugs. Moreover, amino acid molecules provide the interaction sites to improve effectively loading amounts of drugs. 5-Fluorouracil (5-FU) is used as the cargo molecules to observe the delivery in vitro. The results indicate that the maximum loading amounts of drugs are up to 392 mg/g at 60 °C for 12 h in the nanocomposite Phe-LDH@MS. All the nanocomposites exhibit the sustained release of 5-FU at pH 4 and pH 7.4. The Korsmeyer–Peppas model is used to fit the kinetic plot of the drug release in vitro, which concludes that 5-FU release from AA-LDH@MS belongs to Fickian diffusion.

Novel plate-stratiform nanostructured Bi12O17Cl2 was studied with its visible-light photocatalytic performance. The Bi12O17Cl2 photocatalyst synthesized by a solid-state reaction was constructed of dozens of primary nanosheets, which were stacked by a parallel array of ultrathin secondary nanosheets. The microstructure and crystal structure of Bi12O17Cl2 primary and secondary nanosheets were discovered by high-resolution transmission electron microscopy and selected-area electron diffraction analyses. Its absorption edge was determined as about 590 nm and the band gap energy was 2.1 eV. The Bi12O17Cl2 nanomaterial exhibited superior visible-light-responsive photocatalytic activity and confirmed successful photodegradation of methyl orange (MO) under visible-light irradiation. The degradation efficiency was up to 97% in 90 min. Furthermore, the Bi12O17Cl2 photocatalyst exhibited excellent photostability and high mineralization capacity for MO photodegradation reaction. The MO photodegradation process was dominated by the direct photocatalytic mechanism. The contribution from its morphology and microstructure to superior photocatalytic activity was discussed.

Zero Valent Iron nanoparticles (nZVI) were synthesized and immobilized on electrospun carbon nanofibers (ECNFs) surface in a controllable manner through redox reaction. The novel nanomaterial, ECNFs-supported nZVI (nZVI@ECNFs), were evaluated for Cr(VI) ions removal from water for the first time. nZVI@ECNFs outperformed stand-alone nZVI as well as state-of-the-art nZVI research for Cr(VI) remediation in water. nZVI@ECNFs with 0.4 g/L nZVI loading could remove 100% Cr(VI) from 50 mg/L Cr(VI) aqueous solution in as little as 5 min at pH = 4. This is enabled by coupling nanofibrous form ECNFs with dispersed distribution of individual and/or cluster nZVI on surface of ECNFs. It is envisioned that nZVI@CNFs is going to serve as a novel supported nZVI nanomaterial for super-fast heavy metal remediation in ground water and waste water treatment with adjustable high capacity as well as straightforward and energy-saving heavy metal recovery.

Due to the potential applications to high-efficiency and light-weight solar cells, the growth of CuInGaSe2 (CIGS) nanoparticles is a recent research focus. We have developed a relatively simple solvothermal route to grow high quality CIGS nanoparticles in an autoclave under different temperatures (170 – 280°C). The effect of reaction temperature on the shape of CIGS nanoparticles has been investigated. At lower temperatures, the CIGS particles show plate-like shape. Whereas at higher temperatures, most of them exhibit rod-like feature. The nanoparticle products have been also characterized by field emission scanning electron microscopy and X-ray diffraction techniques.

Composite photocatalysts comprised of two semiconducting oxides, with suitable band gaps and band positions, have been reported as an effective approach to enhance photocatalytic activity in the visible region of the electromagnetic spectrum. Here, we report the synthesis, characterization, and photocatalytic evaluations of semiconducting composites made by combing bismuth oxide with either tantalum oxynitride or tantalum nitride. Visible light active composites were synthesized using solution chemistry synthesis method. The composites were characterized by powder X- ray diffraction (PXRD), diffuse reflectance UV-Vis spectroscopy, and photoluminescence (PL). Their photocatalytic activities were evaluated for generation of hydrogen from an aqueous methanol solution under visible light irradiation (λ≥ 420 nm). The as-prepared composite catalysts are found to have longer photogenerated charge-carrier life time, resulting in enhanced photocatalytic activities.

In this study, crystal orientation and polymorphism formation in electrospun poly(vinylidene fluoride) (PVDF)/polyacrylonitrile (PAN) blend fibers after melt-recrystallization were studied. To achieve uniform alignment of electrospun fibers, mechanical stretching was applied to the as-spun nonwoven fibers at 110 °C. Pure ferroelectric β-PVDF crystals in the PAN matrix were achieved, and both polar β-PVDF and polar PAN crystals oriented with their chain axes parallel to the fiber axes. After melt-recrystallization of PVDF, a significant amount of ferroelectric β crystals was retained in addition to the formation of nonpolar α crystals. A polarized Fourier transform infrared study showed that the degree of orientation of ferroelectric β-PVDF crystals was higher than that of nonpolar α crystals, suggesting that the β-PVDF crystals should form at the PVDF/PAN interfaces because of strong dipolar and hydrogen bonding interactions between vinylidene fluoride and acrylonitrile units. The nonpolar α-PVDF crystals should form in the center of PVDF domains.

The study of interactions between a high-power laser and atoms has been one of the fundamental and interesting topics in strong field physics for decades. Based on a nonperturbative model, ten years ago, we developed a set of programs to facilitate the study of interactions between a circularly polarized laser and atomic hydrogen. These programs included only contribution from the bound states of the hydrogen atom. However, as the laser intensity increases, contribution from continuum states to the excitation and ionization processes becomes larger and can no longer be neglected. Furthermore, because the original code is not able to add this contribution directly due to its many disadvantages, a major upgrade of the code is required before including the contribution from continuum states in future. In this paper, first we deduce some important formulas for contribution of continuum states and present modifications and tests for the upgraded code in detail. Second we show some comparisons among new results, old results from the original codes and the available experimental data. Overall the new result agrees with experimental data well. Last we present our calculation of above-threshold ionization (ATI) rate and compare it with a pertuba-tive calculation. The comparison shows that our nonperturbative calculation can also produce ATI peak suppression.

The clogging of the Submerged Entry Nozzle (SEN) duringbillet continuous casting of mid-carbon steel is studied.Clogging materials and inclusions in steel samples taken atladles, tundish and billets are investigated. The total oxygen onthe whole section of the billet is measured. Steel cleanliness atunsteady casting states, including cast start, ladle change, SENchange, cast end, and the special unsteady pouring periodinduced by SEN clogging, are studied. Fluid flow and inclusionmotion and entrapment to SEN surface are also simulated.