Crystallization of UHMWPE nanocomposites filled by multi-wall carbon nanotubes

Journal of Thermal Analysis and Calorimetry - In order to study the effect of MWCNTs on the crystallization of UHMWPE, the UHMWPE nanocomposites filled by MWCNTs with high content were prepared by...     

Desorption of polycyclic aromatic hydrocarbons from soot surface: pyrene and fluoranthene

The kinetics of thermal desorption of two four-ring polycyclic aromatic hydrocarbons, fluoranthene, and pyrene from well-characterized laboratory-generated kerosene soot surface was studied over the temperature range 260-320 K in a low-pressure flow reactor combined with an electron-impact mass spectrometer. Two methods were used to measure the desorption rate constants: monitoring of the surface-bound fluoranthene and pyrene decays due to desorption using off-line HPLC measurements of their concentrations in soot samples, and monitoring of the desorbed molecules in the gas phase using in situ mass spectrometric detection. Results obtained with the two methods were in good agreement and yielded the following Arrhenius expressions for the desorption rate constants: k(des) (fluoranthene) = 4 x 10(14) exp[-(93900 +/- 1700)/RT] and k(des) (pyrene) = 6 x 10(14) exp[-(95200 +/- 1800)/RT] (k(des) are in units of s(-1), and activation energies are in J mol(-1)). In addition, the combined uptake coefficient of fluoranthene and pyrene on soot (calculated using specific surface area) was estimated to be near 5 x 10(-3) at T = 310 K.     

Photodegradation of methyl green using visible irradiation in ZnO suspensions: determination of the reaction pathway and identification of intermediates by a high-performance liquid chromatography-photodiode array-electrospray ionization-mass spectrometry method

Heterogeneous photocatalytic treatment of a dye called methyl green (MG), which was simulating textile wastewater from associated auxiliary chemicals, was investigated using ZnO. A detailed investigation of the photodegradation of MG has been carried out in the ZnO suspension irradiated with visible light. The effects of various factors - viz. pH values, amount of catalyst, initial dye concentration, and the presence of NaCl, Na(2)CO(3), H(2)O(2), and Na(2)S(2)O(8) - on the degradation efficiency were studied. Thirty-two intermediates were separated, identified, and characterized by high-performance liquid chromatography-photodiode array-electrospray ionization-mass spectrometry (HPLC-ESI-DAD-MS) technology, giving us insight into the pathways of the degradation process.     

Heterogeneous Photocatalytic Recycling of FeX2/FeX3 for Efficient Halogenation of C−H Bonds Using NaX

Environmental-friendly halogenation of C−H bonds using abundant, non-toxic halogen salts is in high demand in various chemical industries, yet the efficiency and selectivity of laboratory available protocols are far behind the conventional photolytic halogenation process which uses hazardous halogen sources. Here we report an FeX₂ (X=Br, Cl) coupled semiconductor system for efficient, selective, and continuous photocatalytic halogenation using NaX as halogen source under mild conditions. Herein, FeX₂ catalyzes the reduction of molecular oxygen and the consumption of generated oxygen radicals, thus boosting the generation of halogen radicals and elemental halogen for direct halogenation and indirect halogenation via the formation of FeX₃. Recycling of FeX₂ and FeX₃ during the photocatalytic process enables the halogenation of a wide range of hydrocarbons in a continuous flow, rendering it a promising method for applications.     

A Thiophene Backbone Enables Two-Dimensional Poly(arylene vinylene)s with High Charge Carrier Mobility

Linear conjugated polymers have attracted significant attention in organic electronics in recent decades. However, despite intrachain π-delocalization, interchain hopping is their transport bottleneck. In contrast, two-dimensional (2D) conjugated polymers, as represented by 2D π-conjugated covalent organic frameworks (2D c-COFs), can provide multiple conjugated strands to enhance the delocalization of charge carriers in space. Herein, we demonstrate the first example of thiophene-based 2D poly(arylene vinylene)s (PAVs, 2DPAV-BDT-BT and 2DPAV-BDT-BP , BDT=benzodithiophene, BT=bithiophene, BP=biphenyl) via Knoevenagel polycondensation. Compared with 2DPAV-BDT-BP , the fully thiophene-based 2DPAV - BDT - BT exhibits enhanced planarity and π-delocalization with a small band gap (1.62 eV) and large electronic band dispersion, as revealed by the optical absorption and density functional calculations. Remarkably, temperature-dependent terahertz spectroscopy discloses a unique band-like transport and outstanding room-temperature charge mobility for 2DPAV-BDT-BT (65 cm² V⁻¹ s⁻¹), which far exceeds that of the linear PAVs, 2DPAV-BDT-BP , and the reported 2D c-COFs in the powder form. This work highlights the great potential of thiophene-based 2D PAVs as candidates for high-performance opto-electronics.     

A Modular Tubular Flow System with Replaceable Photocatalyst Membranes for Scalable Coupling and Hydrogenation

Heterogeneous photocatalysis is effective for the selective synthesis of value-added chemicals at lab-scale, yet falls short of requirements for mass production (low cost and user friendliness). Here we report the design and fabrication of a modular tubular flow system embedded with replaceable photocatalyst membranes for scalable photocatalytic C−C, C−N homocoupling and hydrogenation reactions, which can be operated in either circular and continuous flow mode with high performance. The photocatalyst membranes almost fully occupy the volume of the reactor, thus enabling optimal absorption of the incident light. Additionally, the porous structured photocatalyst membranes facilitate the mass transfer of the reactants to efficiently use the active sites, resulting in 0^th-order reaction kinetics and a high space-time yield compared to the batch reaction system at practical application levels and prolonged reaction times.     

Ultrahigh-Rate Na/Cl2 Batteries Through Improved Electron and Ion Transport by Heteroatom-Doped Bicontinuous-Structured Carbon

Rechargeable sodium/chlorine (Na/Cl₂) batteries are emerging candidates for sustainable energy storage owing to their superior energy densities and the high abundance of Na and Cl elements. However, their practical applications have been plagued by the poor rate performance (e.g., a maximum discharge current density of 150 mA g⁻¹), as the widely used carbon nanosphere cathodes show both sluggish electron-ion transport and reaction kinetics. Here, by mimicking the sufficient mass and energy transport in a sponge, we report a bicontinuous-structured carbon cubosome with heteroatomic doping, which allows efficient Na⁺ and electron transport and promotes Cl₂ adsorption and conversion, thus unlocking ultrahigh-rate Na/Cl₂ batteries, e.g., a maximum discharge current density of 16,000 mA g⁻¹ that is more than two orders of magnitude higher than previous reports. The optimized solid–liquid–gas (carbon–electrolyte–Cl₂) triple interfaces further contribute to a maximum reversible capacity and cycle life of 2,000 mAh g⁻¹ and 250 cycles, respectively. This study establishes a universal approach for improving the sluggish kinetics of conversion-type battery reactions, and provides a new paradigm to resolve the long-standing dilemma between high energy and power densities in energy storage devices.     

Chemistry and Applications of Functionalized 2,4-Thiazolidinediones

Thiazolidinedione (TZD) is one of the privileged heterocyclic rings and has shown many biological applications in medicinal chemistry and drug discovery. This review covers the synthetic approaches of TZD and its derivatives, different synthetic techniques for affording the desired regioselectivity and stereoselectivity, and the techniques that would enhance reaction conditions such as microwave, one-pot, or ultrasound synthesis. It focuses on synthetic challenges of glitazones and the transformation of other heterocycles to TZD. Moreover, the chemical and biological behavior of TZD through the substitution in the N3 position, modification of the C5 position, annealing in complex heterocyclic systems, and hybridization with other pharmacologically attractive moieties are discussed. All reactions mentioned are provided as possible with different reaction conditions, mechanisms, derivatives scope, yield and clarified by applications of such reactions in the construction of potential medicinal agents. The review also answers questions about rapid racemization of glitazones, their toxicity, considering TZD as pan-assay interference compounds (PAINS) or not, and the influence of saturation of 5-position of TZD in their biological activities. This review is a comprehensive guide to make informed decisions for construction of TZD derivatives with biological potentials.     

集成光学波导光栅研究进展

报道了20世纪80年代以来,研究组在集成光学波导光栅研究领域的主要工作及研究成果。其中包括集成光学波导光栅的制备研究;若干非线性波导光栅器件研究;高效体相位全息布拉格光栅-光导板的耦合互连;单片集成波导光栅波分复用等。这些研究工作为光通信、光计算、光传感和光学信息处理等应用领域提供小型化、低功耗、超快速全光型器件奠定了技术基础。     

非线性一维光子晶体光开关与光双稳

设计和制备了ZnS/ZnSe叠层共 2 0个周期的非线性一维光子晶体光开关与光双稳器件 理论模拟了波长 5 14 .5nm的氩离子激光 ,在阈值功率密度 1.0× 10 5W/cm2 下 ,完全移出光子禁带 ,实现了光开关 同一器件也可作为光学双稳器件 ,实验测出其阈值功率密度为 1.38× 10 5W/cm2 ,双稳开关时间为 10 0ps 理论与实验结果基本一致