Xuzhou Institute of Technology

About: Xuzhou Institute of Technology is a education organization based out in Xuzhou, China. It is known for research contribution in the topics: Catalysis & Computer science. The organization has 1696 authors who have published 1521 publications receiving 13541 citations.

One-step hydrothermal synthesis of high-performance visible-light-driven SnS2/SnO2 nanoheterojunction photocatalyst for the reduction of aqueous Cr(VI)

Abstract: A simple and cost-effective one-step hydrothermal method, which was based on the reactions of tin(IV) chloride pentahydrate and different dosages of thioacetamide in water at 190 °C for 6 h, was employed for the synthesis of composition-tunable SnS 2 /SnO 2 nanoheterojunctions (e.g., SnS 2 /SnO 2 -A, SnS 2 /SnO 2 -B and SnS 2 /SnO 2 -C). The photocatalytic properties of the as-synthesized SnS 2 /SnO 2 nanoheterojunctions were tested by the reduction of aqueous Cr(VI) under visible-light ( λ > 420 nm) irradiation. Furthermore, the photocatalytic efficiency of SnS 2 /SnO 2 -B was compared with those of PM-SnS 2 /SnO 2 (which denotes the physically mixed SnS 2 /SnO 2 nanocomposite with the same composition as SnS 2 /SnO 2 -B) and SnS 2 nanoflakes at different dosages of photocatalysts. It was observed that (i) the photocatalytic activities of the as-synthesized SnS 2 /SnO 2 nanoheterojunctions depended on their compositions, and SnS 2 /SnO 2 -B with 70 mol% SnS 2 displayed the highest photocatalytic activity; (ii) SnS 2 /SnO 2 -B invariably exhibited higher photocatalytic efficiencies than PM-SnS 2 /SnO 2 and SnS 2 nanoflakes at different dosages of photocatalysts; (iii) the washing with 1 mol/L HNO 3 can effectively regenerate the used photocatalyst; (iv) SnS 2 /SnO 2 -B exhibited good photocatalytic stability in reuses, with regeneration by 1 mol/L HNO 3 -washing after each cycle of photocatalytic use; and (v) Cr(VI) was reduced to Cr(III). The possible formation mechanism of SnS 2 /SnO 2 nanoheterojunctions and the reasons accounting for the photocatalytic results were also discussed.

Catalytic Asymmetric Inverse‐Electron‐Demand Oxa‐Diels–Alder Reaction of In Situ Generated ortho‐Quinone Methides with 3‐Methyl‐2‐Vinylindoles

Abstract: The first catalytic asymmetric inverse-electron-demand (IED) oxa-Diels–Alder reaction of ortho-quinone methides, generated in situ from ortho-hydroxybenzyl alcohols, has been established. By selecting 3-methyl-2-vinylindoles as a class of competent dienophiles, this approach provides an efficient strategy to construct an enantioenriched chroman framework with three adjacent stereogenic centers in high yields and excellent stereoselectivities (up to 99 % yield, >95:5 d.r., 99.5:0.5 e.r.). The utilization of ortho-hydroxybenzyl alcohols as precursors of dienes and 3-methyl-2-vinylindoles as dienophiles, as well as the hydrogen-bonding activation mode of the substrates met the challenges of a catalytic asymmetric IED oxa-Diels–Alder reaction.

Lump and lump-soliton solutions to the $$(2+1)$$ ( 2 + 1 ) -dimensional Ito equation

Abstract: Based on the Hirota bilinear form of the $$(2+1)$$ -dimensional Ito equation, one class of lump solutions and two classes of interaction solutions between lumps and line solitons are generated through analysis and symbolic computations with Maple. Analyticity is naturally guaranteed for the presented lump and interaction solutions, and the interaction solutions reduce to lumps (or line solitons) while the hyperbolic-cosine (or the quadratic function) disappears. Three-dimensional plots and contour plots are made for two specific examples of the resulting interaction solutions.

Carbonized polyaniline activated peroxymonosulfate (PMS) for phenol degradation: Role of PMS adsorption and singlet oxygen generation

Abstract: N-doped carbonaceous materials are promising efficient catalysts for peroxymonosulfate (PMS) activation In this study, the high-efficient N-doped carbon materials were prepared by direct carbonization of polyaniline (PANI) at 700 °C–1000 °C It was optimized that the CPANI-9 (carbonized polyaniline prepared at 900 °C) exhibited excellent catalytic performance to activate PMS for phenol degradation, which was efficient over a wide pH range (pH 35∼9) In the CPANI-9/PMS system, the PMS adsorption/activation was identified as the key step determining the reaction rate The quenching experiments and electron paramagnetic resonance demonstrated that the non-radical pathway was dominant in phenol degradation and singlet oxygen (1O2) was the main active specie Graphitic N, pyridinic N, defects and ketonic groups (C O) were identified as catalytic sites Interestingly, only the presence of PO43− greatly decreased the phenol degradation rate and PMS decomposition The CPANI-9/PMS system could also degrade effectively various organic pollutants, indicating that it had potential practical application