Hydrothermal Synthesis and Structural Characterization of a Novel 3-D Open Framework Zinc Phosphate Microporous Compound(C_5N_2H_(14))·[Zn_3(OH_2)(PO_4)_2(HPO_4)]

One novel organically templated zincophophate(C5N2H14)·[Zn3(OH2)(PO4)2(HPO4)] has been synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction together with elemental analysis, infrared spectroscopy, thermogravimetric analysis, and powder X-ray diffraction. The title compound crystallizes in the monoclinic space group P21/n, with a = 9.7904(11), b = 14.0287(14), c = 11.8651(13) , β = 104.690(3), V = 1576.4(3) 3, Z = 4, T = 296(2) K, Mr = 601.31 and Dc = 2.533 g/cm3. The compound consists of a macroanionic [Zn3(OH2)(PO4)2(HPO4)]2- framework and(C5N2H14)2+ cations, and its structure is built up from ZnO3(OH2), ZnO4, HPO4 and PO4 tetrahedral units that result in 4, 8 and 10-ring channels.     

A New 2D Barium-organic Framework Built from 1H-Benzimidazole-5,6-dicarboxylate with Luminescent and Antibacterial Studies

A new 2D barium-organic framework, [Ba2(Hbidc)2]n(1, Hbidc = 1H-benzimidazole-5,6-dicarboxylate), has been solvothermally synthesized and structurally characterized by elemental analysis, IR spectroscopy, TGA, powder X-ray diffraction, and single-crystal X-ray diffraction. The crystal belongs to the triclinic system, space group P1 with a = 6.8785(14), b = 9.4558(19), c = 14.641(3) , α = 86.22(3), β = 82.27(3), γ = 88.40(3)°, V = 941.4(3) 3, Z = 2, Mr = 682.96, Dc = 2.409 g/cm3, μ(MoKα) = 4.217 mm-1, F(000) = 640, the final R = 0.0587 and wR = 0.1619 for 3030 observed reflections with I 2σ(I). Structural determination reveals that 1 exhibits an interesting 2D layer structure constructed by carboxylate groups of Hbidc ligands and shows good thermal stability(up to 400 ℃). Solid-state 1 emits intense indigotin photoluminescence with fluorescence lifetime of 62.13(408 nm) at room temperature. The H3bidc ligand and its barium complex have been screened for antibacterial activity against several bacteria strains, and the results are compared with the activity of penicillin.     

Synthesis,Structure and Magnetic Property of One Ni~Ⅱ Based Coordination Polymer

One new coordination polymer, [Ni(m-bix)(m-BDC)](1, m-bix = 1,3-bis(imidazol-1-ylmethyl)benzene, m-BDC = 1,3-benzenedicarboxylic acids), has been hydrothermally synthesized and structurally characterized by elemental analysis, IR, TGA and X-ray single-crystal diffraction. The green block crystal of complex 1(C22H18N4Ni O4) belongs to monoclinic system, space group P21/c with a = 10.0418(3), b = 23.8651(6), c = 8.7872(2) A, β = 112.333(3)o, V = 1947.88(9)A3, Z = 4, Dc = 1.572 g/cm3, Mr = 461.11, F(000) = 952, R = 0.0335 and w R = 0.0683 for 2827 observed reflections(I 2σ(I)). Complex 1 exhibits a novel 6-connected 3D sxd type topological framework. The magnetic characterization of complex 1 shows antiferromagnetic coupling exchange.     

Studies on crystal transition of polyamide 11 nanocomposites by variable-temperature X-ray diffraction

Polyamide I1 （PAll） and its nanocomposites with different organoclay loadings were prepared by melt-compounding and subsequent pelletizing. The crystal phase transitions of PAl 1 and its clay nanocomposites were investigated by variable-temperature X-ray diffraction. It was found that the Brill transition of the nanocomposite was 20 K higher than that of the neat PAl 1 for both heating and cooling processes. The PAl 1 d-spacings of the nanocomposites were observed to be smaller than those of the neat PAl 1 for melt crystallization. The constraints imposed by the addition of layered clay, restricting the thermal expansion of the polymer chains, are probably responsible for such a reduction of the d-spacing.     

基于无衍射光的表面粗糙度三角测量及其灰色评定方法

 激光三角法是表面形貌非接触测量中的一种常用方法,在几何测量领域应用广泛。传统的激光三角法采用高斯光束作为指示光源,在机械扫描机构的配合下,通过对被测表面逐点扫描完成表面形貌的测量。采用新型的无衍射光替代传统激光光源,解决了普通高斯光束存在的“焦深”问题,简化了机械结构。并采用基于灰色系统理论的灰色滤波进行表面形貌的分离与评定,克服了原有方法对测量数据样本量和统计特性的依赖,并通过实验表明该系统能够准确地完成表面形貌的三维测量,所提出的灰色评定方法能够比较有效地进行表面形貌的分离与评定。     

利用TeO2减少多模光纤出射场散斑干扰的研究

 为了减少多模光纤出射光场的散斑干扰,提出了把声光布拉格衍射效应所形成的不同衍射级耦合到多模光纤中,由于衍射级具有不同的偏振态,消弱了光场相干条件,进而在出射光场中消弱了散斑场的对比度,并通过对改变声场频率后得到的散斑场对比度的分析,证实了利用各向异性晶体TeO2能够控制散斑场对比度,改善出射场的高斯分布,得出了可以利用布拉格衍射效应减少散斑场干扰的可能性。     

强激光条件下5CB液晶中的激光诱导衍射环现象

强激光经5CB液晶传播时会产生非线性自相位调制现象,利用532 nm和1 064 nmCW激光研究了强激光条件下5CB液晶中的激光诱导衍射环现象,并对强激光在5CB液晶中产生自相位调制的现象和机理进行了讨论.当532 nm激光和1 064 nm激光功率密度分别大于10 kW/cm2和300W/cm2时,接收白屏上有较明...     

用于非球面点衍射检测的最佳匹配球参量获取方法研究

针对非球面点衍射干涉检测中的欠采样问题,为了减小干涉条纹的密度,提出了一种基于最小反射会聚光斑半径求解最佳匹配球球心位置的方法.首先分析了获取最佳匹配球球心位置对实现非球面光学元件高准确度面形检测所起的重要作用,指出了以最小反射会聚光斑作为最佳匹配球球心位置的判断依据;然后运用光线追迹和迭代法推导了最佳匹配球球心位置的...     

高温高压固态复分解反应法生长氮化镓的应变性质研究

本文采用高温高压下固态复分解反应法生长氮化镓.用X射线衍射仪、扫描电子显微镜、激光拉曼光谱仪对其进行分析,结果表明生成了六角纤锌矿结构的氮化镓晶体.该样品在宏观上受到了张应力的作用,退火后,宏观的应变状态由张应变向压应变转变;晶体微观应力减小,晶粒尺寸变大,晶体质量变好.     

爆轰法合成碳包覆镍纳米颗粒的研究

 采用自制的负氧平衡复合炸药前驱体,在密闭容器中充氮气保护下爆轰合成了碳包覆镍纳米颗粒。利用X射线衍射、X射线荧光、透射电镜和拉曼光谱等技术,对爆炸产物的组成成分、结构形貌等进行了观测。结果表明,爆轰产物主要由具有面心立方结构的镍晶核和碳元素构成,此外还含有其它微量元素;合成的纳米颗粒呈球形或椭球形状,颗粒尺寸主要分布在10~25 nm范围,包覆的碳壳厚度约1~2 nm,核壳结构完备。结合观测结果,对爆轰法合成碳包覆纳米颗粒的形成机制进行了简单的讨论。