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991.
Ligand bridged polymeric complexes of the type [M(apainh)(H2O)X] where, M=Mn(II), Co(II), Ni(II), Cu(II), and Zn(II); X=Cl2 or SO4; apainh=acetone p‐amino acetophenone isonicotinoyl hydrazone have been synthesized and characterized. The complexes are stable solids, insoluble in common organic solvents and are non‐electrolytes. Magnetic moments and electronic spectral studies suggest a spin‐free octahedral geometry for all Mn(II), Co(II), Ni(II), and Cu(II) complexes. IR spectra show tridentate nature of the ligand bonding through two >C?N and a >C?O groups. X‐ray powder diffraction parameters for some of the complexes correspond to orthorhombic and tetragonal crystal lattices. Thermal studies (TGA and DTA) of [Mn(apainh)(H2O)SO4] complex show multi‐step decomposition pattern of both an endothermic and exothermic nature. ESR data of Cu(II) chloride complex in solid state show an axial spectra, whereas, Cu(II) sulfate complex is isotropic in nature. The complexes show a significant antifungal activity against a number of pathogenic fungal species and antibacterial activity against Pseudomonas sp. and Clostridium sp. The metal complexes are more active than the ligand. 相似文献
992.
Mousa Ghaemy Samaneh Sharifi Seyed Mojtaba Amini Nasab Mehdi Taghavi 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(5):487-497
Two new symmetrical diamines were designed and synthesized having different functional groups such as a pair of phenyl ether linkages, 2,3-diaryl substituted imidazole rings and CF3 groups as pendant, and characterized by FT-IR, 1H and 13C-NMR spectroscopy and elemental analysis. A series of new fluorescent poly(imide-ether)s (PIEs) was prepared by polymerization of the diamines with commercial tetracarboxylic dianhydrides such as pyromellitic dianhydride and 3,3′,4,4′-benzophenone tetracarboxylic dianhydride. The resulting PIEs were amorphous and had intrinsic viscosity [η] in the range of 0.42–0.51 dL/g. The weight average molecular weights (Mw) of these polymers were measured by GPC and were in the range of 28658–35595 g/mol with molecular weight distribution (MWD) of 2.12–2.27. These polymers were readily soluble in a variety of organic solvents and formed low-colored and flexible thin films with cut-off wavelength (λ0) in the range of 385–420 nm, and all PIEs films exhibited high optical transparency. They also possessed good thermal stability with 10% weight loss temperatures (T10%) in the range 486–537°C in N2. The glass transition temperatures (Tg) of PIEs are in the range 251–324°C. These polymers showed fluorescence emission in film and in solution at 459–476 nm with the quantum yields in the range 4–12%. 相似文献
993.
The flammability and the thermal oxidative degradation kinetics of expandable graphite (EG) with magnesium hydroxide (MH) in flame‐retardant polypropylene (PP) composites were studied by limiting oxygen index (LOI), UL‐94 test, and thermogravimetric analysis (TGA). The results show that EG is a good synergist for improving the flame retardancy of PP/MH composite and the effect is enhanced with decreasing EG particle size. The Kissinger method and Flynn‐Wall‐Ozawa method were used to determine the apparent activation energy (E) for degradation of PP and flame retarded PP composites. The data obtained from the TGA curve indicate that EG markedly increases the thermal degradation temperature of PP/MH composites and improves the thermal stability of the composites. The kinetic results show that the values of E for degradation of flame retarded PP composites is much higher than that of neat PP, especially PP/MH composites with suitable amount of EG, which indicates that the flame retardants used in this work have a great effect on the mechanisms of pyrolysis and combustion of PP. 相似文献
994.
Gas chromatography (GC) is an analytical tool very useful to investigate the composition of gaseous mixtures. The different gases are separated by specific columns but, if hydrogen (H2) is present in the sample, its detection can be performed by a thermal conductivity detector or a helium ionization detector. Indeed, coupled to GC, no other detector can perform this detection except the expensive atomic emission detector. Based on the detection and analysis of H2 isotopes by low‐pressure chemical ionization mass spectrometry (MS), a new method for H2 detection by GC coupled to MS with an electron ionization ion source and a quadrupole analyser is presented. The presence of H2 in a gaseous mixture could easily be put in evidence by the monitoring of the molecular ion of the protonated carrier gas. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
995.
Sandeep Ippalapalli A. Dileep Ranaprathapan Dr. Sachchida N. Singh Dr. G. Harikrishnan 《Chemphyschem》2013,14(6):1190-1196
Two‐way multicomponent diffusion processes in polymeric nanocomposite foams, where the condensed phase is nanoscopically reinforced with impermeable fillers, are investigated. The diffusion process involves simultaneous outward permeation of the components of the dispersed gas phase and inward diffusion of atmospheric air. The transient variation in thermal conductivity of foam is used as the macroscopic property to track the compositional variations of the dispersed gases due to the diffusion process. In the continuum approach adopted, the unsteady‐state diffusion process is combined with tortuosity theory. The simulations conducted at ambient temperature reveal distinct regimes of diffusion processes in the nanocomposite foams owing to the reduction in the gas‐transport rate induced by nanofillers. Simulations at a higher temperature are also conducted and the predictions are compared with experimentally determined thermal conductivities under accelerated diffusion conditions for polyurethane foams reinforced with clay nanoplatelets of varying individual lamellar dimensions. Intermittent measurements of foam thermal conductivity are performed while the accelerated diffusion proceeded. The predictions under accelerated diffusion conditions show good agreement with experimentally measured thermal conductivities for nanocomposite foams reinforced with low and medium aspect‐ratios fillers. The model shows higher deviations for foams with fillers that have a high aspect ratio. 相似文献
996.
利用吡啶-3-甲酸与Cy3SnOH反应合成了[(C5H4N)COOSnCy3]n,经元素分析、1H NMR、IR和X-射线衍射表征分子结构。在该配合物的结构中,中心Sn原子呈现五配位畸变三角双锥构型,并通过分子间的N→Sn配位形成一维链状线型聚合物,分子链间的C-H…O氢键作用将配合物分子组装成三维超分子网络结构。利用量子化学G03W软件,在LANL2DZ基组对配合物的稳定性、前沿分子轨道组成及能量进行研究。热重分析表明该化合物在273℃开始发生分解。 相似文献
997.
利用不同过渡金属盐在溶剂热中合成了2个新型杂核化合物{[CuEu2(INAIP)3(HCOO)(H2O)3]·3H2O}n(1)和{[NiEu2(INAIP)4(H2O)4]·4H2O}n(2)(INAIP=异烟酰胺吡啶基异酞酸根),并对其进行了元素分析、IR及X-射线衍射法表征。晶体结构研究表明:配合物1和2都属于三斜晶系,P1空间群。晶胞参数:配合物1a=1.0887(3)nm,b=1.5158(4)nm,c=1.5644(2)nm,V=2.3332(10)nm3,Z=2,Dc=1.955g·cm-3,μ=3.203mm-1,F(000)=1352,Rint=0.027,R1=0.0505,wR2=0.1309。配合物2a=1.0134(3)nm,b=1.0836(6)nm,c=1.3741(2)nm,V=1.4530(9)nm3,Z=1,Dc=1.878g·cm-3,μ=2.554mm-1,F(000)=818,Rint=0.0458,R1=0.0341,wR2=0.0869。配合物1是由配体异烟酰胺吡啶基异酞酸连接而成的三维二重贯穿sqc27拓扑结构,而配合物2是由配体异烟酰胺吡啶基异酞酸连接稀土铕离子形成二维层状结构,该二维层通过Ni-O和Ni-N键连接成三维非贯穿网络结构。配合物1和2具有典型的稀土铕离子红色荧光和高的热稳定性。 相似文献
998.
本文通过3,6-二肼基-1,2,4,5-四嗪(DHT)分别与高氯酸和硝酸反应得到2种高氮含能离子盐,并通过X-射线单晶衍射技术对它们的结构进行了表征。(DHT)(NO3)2(1)属于单斜晶系,C2/c空间群,晶胞参数:a=1.3000(6)nm,b=0.8349(3)nm,c=1.0187(5)nm,β=118.89(5)°,Z=4;(DHT)(ClO4)2(2)属于正交晶系,P21212空间群,晶胞参数:a=0.9804(4)nm,b=1.0747(4)nm,c=0.5325(2)nm,Z=2。采用DSC和TG-DTG技术研究了这两种含能离子盐的热分解机理,并对这两种含能离子盐的非等温动力学、爆热及感度进行了测试分析。研究表明这两种含能离子盐在敏感型含能材料领域具有潜在的应用前景。 相似文献
999.
对炭泡沫为支撑骨架的氧化硅气凝胶(SiO2/炭泡沫)和碳化硅(SiC/炭泡沫)复合材料分别采用XRD、SEM、激光导热仪、万能力学试验机进行物相、微观结构、热学及力学性能方面的表征.结果表明:所制备的SiO2/炭泡沫与原炭泡沫相比,具备更高的抗压强度(14.95 MPa)和更低的室温热导率(0.44 W·m-1·K-1).SiC/炭泡沫材料则保持了较高的抗压强度值(14.66 MPa),其在 1 200 ℃下具备极低的高温热导率(2.18W·m-1·K-1).热重分析表明,SiC/炭泡沫在氧化氛围中到610 ℃才发生质量的损失,而内部炭发生完全烧蚀的温度高达844 ℃,这表明该材料的抗氧化性能远好于纯的炭泡沫材料. 相似文献
1000.
酒石酸铅锆的制备、表征及其燃烧催化作用 总被引:1,自引:0,他引:1
以酒石酸、硝酸氧锆和硝酸铅为原料,合成出了双金属盐酒石酸铅锆,采用有机元素分析、X射线荧光光谱和FTIR对其进行了表征。在程序升温条件下,利用TG/DTG、DSC、固相原位反应池/FTIR联用技术,研究了酒石酸铅锆的热行为和热分解机理,描述了酒石酸铅锆的热分解过程,分析得出其最终分解产物为ZrO2、PbO和C。利用螺压工艺制备了含酒石酸铅锆的推进剂样品,研究了酒石酸铅锆对双基系推进剂燃烧性能的影响,分析了其燃烧催化作用。结果表明,酒石酸铅锆对双基系推进剂的燃烧具有良好的催化作用,是一种高效的燃烧催化剂;酒石酸铅锆热分解的最终产物PbO是催化燃烧的主要活性物质,推进剂燃烧过程中形成了氧化铅-铅循环催化体系,而锆和碳则起辅助催化的作用。 相似文献