聚苯氧基磷酸联苯二酚酯/聚磷酸铵膨胀阻燃剂对环氧树脂阻燃性能影响研究

以聚苯氧基磷酸联苯二酚酯(PBPP)与聚磷酸铵(APP)组成复合阻燃剂,对环氧树脂(EP)进行阻燃改性.通过氧指数(LOI)、垂直燃烧(UL-94)、热失重(TGA)、锥形量热(CONE)和扫描电镜(SEM)等方法研究改性环氧树脂的阻燃性能和阻燃机理.结果表明,PBPP/APP体系对EP具有较好的阻燃性能,阻燃剂添加量为10%时能使环氧树脂的氧指数提高到29.6%,垂直燃烧等级达到UL94 V-0级,残炭量大大增加;平均热释放速率下降45.7%,热释放速率峰值下降51.0%,有效燃烧热平均值下降21.1%;TGA、CONE、SEM等综合分析显示了PBPP/APP改性后的环氧树脂比纯环氧树脂具有更高的热稳定性,燃烧后能够形成连续、致密、封闭、坚硬的焦化炭层,在聚合物表面产生有效覆盖、隔绝了氧气,改善了环氧树脂的燃烧性能.     

Effective transformation of cellulose to 5-hydroxymethylfurfural catalyzed by fluorine anion-containing ionic liquid modified biochar sulfonic acids in water

This article first discloses that the fluorine anion-containing ionic liquids-functionalized biochar sulfonic acids (BCSA-IL-F_1–3s), which were simply synthesized by an ionic exchange of 1-trimethoxysilylpropyl-3-methylimidazolium chloride (IL-Cl) grafted on the BCSA with CF₃SO₃H (HF₁), HBF₄ (HF₂), HPF₆ (HF₃), respectively, can efficiently catalyze cellulose hydrolysis into reducing sugars (RSs) and 5-hydroxymethyl furfural (HMF) in water under microwave irradiation. This process provides a very high catalysis efficiency (turnover numbers, 4.03–4.89) at mild temperature (80 °C) for 3 h, but also possesses an excellent repeatability. More outstandingly, they can achieve much higher HMF yields (12.70–27.94%) compared to the IL-Cl-functionalized BCSA catalyst (HMF yields are lower than 0.1%) under the same reaction conditions. This is likely because the introduction of IL-F_1–3s groups can significantly improve the accessibility, acidity and thermal stability of BCSA’s SO₃H sites, as supported by evidence from a solid ³¹P NMR spectrum and thermogravimetric analysis. It is proposed that the good selectivity for HMF perhaps originates from a co-catalysis action of the IL-F_1–3s and SO₃H groups on BCSA-IL-F_1–3s in the further conversion of RSs to HMF.     

Porous nitrogen-doped graphene for high energy density supercapacitors in an ionic liquid electrolyte

Porous nitrogen-doped graphene (PNG) has been prepared via simple thermal treatment of graphene oxide and urea, and the morphology and structure of the PNG have been characterized by using a range of electron microscopy, X-ray photoelectron spectroscopy, and other techniques. The electrochemical performances of the PNG have been investigated in an ionic liquid electrolyte by cyclic voltammetry and galvanostatic charge-discharge via both three-electrode and two-electrode configurations. The PNG electrode delivers a specific capacitance of 310 F g^?1 at 1 A g^?1 with good cycling stability over 4000 cycles. The high electrochemical performance is ascribed to the porous structure and nitrogen-doping in the PNG. The porous structure enables high specific surface area and rapid ion mobility, contributing to double layer capacitance, while the N-doping enhances electrochemical activity and electric conductivity, contributing to pseudocapacitance. Meanwhile, the ionic liquid electrolyte enables a very wide working voltage of 3 V, leading to a high energy density up to 163.8 W h kg^?1. The fabricated supercapacitor can light up a LED for a long while with low self-discharge, showing good potential for practical application.     

Regioselective Synthesis of Polycyclic and Heptagon-embedded Aromatic Compounds through a Versatile π-Extension of Aryl Halides

A versatile π-extension reaction was developed based on the three-component cross-coupling of aryl halides, 2-haloarylcarboxylic acids, and norbornadiene. The transformation is driven by the direction and subsequent decarboxylation of the carboxyl group, while norbornadiene serves as an ortho-C−H activator and ethylene synthon via a retro-Diels–Alder reaction. Comprehensive DFT calculations were performed to account for the catalytic intermediates.     

An RNA polymerase I-driven human respiratory syncytial virus minigenome as a tool for quantifying virus titers and screening antiviral drug

Human respiratory syncytial virus(RSV) is an important pediatric pathogen of lower respiratory tract worldwide. No vaccines and antiviral drugs are available. Herein the use of an RNA polymerase I-driven RSV minigenome for analyzing RSV replication and screening anti-RSV drugs was investigated. The RNA polymerase I(Pol I) was used to transcribe RSV minigenome from the constructed plasmid, designated p HM-RSV-Gluc, of minigenome c DNA which comprised trailer region, gene start sequence(GS), reverse complementary copy of Gaussia luciferase(Gluc) gene, gene end sequence(GE), and leader region in the direction of 5'–3'end and was flanked by promoter and terminator of Pol I. The expression of Gluc was confirmed in p HM-RSV-Gluc transfected HEp-2 cells following RSV infection and had the characteristics of dose-dependent, which provided a rapid, sensitive, and quantitative method for quantifying virus titers and screening antiviral drugs.     

Ab initio studies on the thermolysis of azetidine

The reaction mechanism of the thermolysis of azetidine to form ethylene and methylen-imine has been studied by ab initio SCF MO method at STO--3G and 3-21G levels. Two possible step-wise pathways are explored. One is the breaking of C--C bond as the first step, while the other is thebreaking of C--N bond. All the stationary points on the potential energy surface (PES) are fully optimiz-ed. MP2 / 3-21G single point calculations on all stationary points and MCSCF / STO-3G computationsfor some stationary points are also carried out. The calculations indicate that azetidine decomposesvia biradicaloid intermediates and the cleavage of C--N bond is preferable to that of C--C bond.     

平菇多糖稀溶液行为的研究

平菇多糖属生物高分子, 文章对平菇多糖稀溶液性质进行了研究。实验系采用Elias浊点滴定法测定平菇多糖溶液的θ组成, 用快速动态膜渗透计和粘度法测定平菇多糖的数均分子量、维利系数与分子链的构型参数。探讨其在θ条件下的分子形态及用Tung函数法等处理分级数据, 从而获得平菇多糖的分子量分布。     

气相二茂铁双电荷离子的动能谱研究

The unimolecular charge separation reactions of the doubly charged ions FeC_(10)H_(10)~(2+)、FeC_(10)H_9~(2+)、FeC_(10)H_8~(2+) produced in the ion source by electron impact from ferrocene have been studied using Mass analyzed Ion Kinetic Energy Spectrometry (MIKES) technique. From the values of the kinetic energy releases (T), the intercharge distances (R) of the exploding doubly charged ions in their transition structures have been estimated and some structural informations about the transition states can be obtained. The collision induced reactions of the FeC_(10)H_(10)~(2+) ion with Ar have been studied using MIKES, we postulate a new type of continuing reaction which may be "collisional charge separation induced dissociation".