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设计和构建了多轴多模式、闭环伺服控制系统的研发平台,实现了用于气相色谱仪的不同结构的两种液体自动进样器的并行设计与研制。基于兼容与互换的思路,开发出一体化嵌入式控制驱动模块,采用相同的直流电机、编码器,电气与机械接口统一标准,实现了上述组件在两种机型间的直接代换。研制的标准型110个样品位和平台型40个样品位两种液体自动进样器,与气相色谱仪联机,采用1μL手动进样针,对于0.5μL十六烷-异辛烷标准液体样品,6个不同瓶位连续6次进样测试,重复进样的信号峰面积RSD分别为1.1%和1.5%,取0.1,0.3,0.5,0.7和0.9μL进样,峰面积与进样量的线性相关系数为0.9947。 相似文献
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Synthesis and Crystal Structure of a New Zn(Ⅱ) Complex Exhibiting Strong Luminescence 总被引:1,自引:1,他引:0
The title complex,[Zn(ip)2(H2O)2][ZnCl4]·H2O·2DMF 1(ip=imidazo[4,5-f][1,10] phenanthroline),has been synthesized via the slow evaporation of concentrated reaction solution at room temperature.It was characterized by single-crystal X-ray diffraction.Crystal data for C32H36Cl4N10O5Zn2:white prism,0.17mm×0.15mm×0.10mm,monoclinic,space group P2/c,a=11.928(8),b=9.868(6),c=16.520(11),β=104.879(12)°,V=1879(2)3,Z=2,Mr=913.25,Dc=1.614 g/cm3,F(000)=932,μ=1.616 mm-1,λ(MoKα)=0.71073,GOOF=1.045,R=0.0710 and wR=0.1755 for 3055 observed reflections with Ⅰ2σ(Ⅰ).X-ray diffraction study reveals that the title complex has an interesting 3D architecture via hydrogen bonding interactions and π-π interactions.The IR,TGA,XRD and luminescent properties of complex 1 were also studied. 相似文献
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Metal-organic frameworks(MOFs), consisting of metal, anion and organic ligands, have attracted much attention. The structure of MOFs is affected by various factors. To explore the effects of metal ions, we synthesized six complexes, namely {[Me_2NH_2][Zn_4(H_2L)(L)]·2 H_2O·2 DMF}_n(1), {[Me_2NH_2]_2[Cd_2(L)]·2H_2O}_n(2), {[Me_2NH_2]_2[Ca_3(L)(μ-OH)_2(DMF)_2]·2H_2O}_n(3) and {[Me_2NH_2]_2[M_2(L)(μ-OH)]· H_2O·2DMF}_n(M = Co, 4; Ni, 5; Mn, 6), from a C_(2v)-based hexacarboxylate ligand([1,1';4',1']terphenyl-3,5,2',5',3',5'-hexacarboxylic acid(H_6L)) using metal-induced strategy. These MOFs were thoroughly characterized by single-crystal and X-ray diffraction, elemental analysis, Fourier-transform infrared spectra(FTIR) and photoluminescence. 相似文献
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A new coordination polymer {[In(bdc)(OH)]·4H2O}n(H2bdc=1,4-benzenedi-carboxylic acid) has been synthesized through hydrothermal conditions,and was characterized by X-ray single-crystal diffraction and other measurements.The complex crystallizes in the orthorhombic system,space group Imma with a=18.3621(13),b=7.1932(5),c=11.8278(8),V=1562.24(19)3,Z=4.Dc=1.565g/cm3,Mr=368.00,F(000)=728,μ(MoKα)=1.542 mm-1,S=1.019,R=0.0468 and wR=0.1326 for 884 observed reflections(2σ(Ⅰ)).The title compound represents a 3-D framework containing four kinds of tunnels in different shapes and sizes. 相似文献
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基于整体便携式气相色谱仪共用开发平台的设计理念,研制出了多功能一体化控制器模块.模块包括控制器、功率驱动组件和信号采集组件,直接嵌入到便携式气相色谱仪中.经试验考核,色谱柱温度波动不高于±0.1℃,60℃/min速率升温波动的RSD低于0.15%,进样口和检测器温度波动不高于±0.1℃,柱压不高于±0.16 KPa.以浓度为1 mg/m3的苯标准样品连续6次自动抽取1 m L样品进样分析,定性和定量重复性偏差RSD分别为0.1%和4.6%(峰高),温湿度试验为0~40℃和95%,振动试验(无运输包装)位移为25.4 mm、加速度为1.5 g,以频率5~200~5 Hz正弦波振动与XYZ轴向振动,试验结果正常.模块应用到3种新型仪器中效果理想,满足现场及野外应用要求,具有通用、坚固、体积小和功耗低等特点. 相似文献
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A mercury(Ⅱ) iodide complex with organosulfide [Hg(pymt)(pymtH)I] 1 (pymt = the anion of pyrimidine-2-thiolate) has been synthesized by slow evaporation of the solution at room temperature and structurally characterized by single-crystal X-ray diffraction. Basic ideas and data collected are given. X-ray diffraction analysis reveals that complex 1 is mononuclear. Crystallographic data: C8H7HgIN4S2, Mr = 550.79, monoclinic system, space group P21/c, a = 11.218(4), b = 9.551(3), c = 15.877(4) A^°, β = 129.697(15)°, V = 1308.9(7) A^°^3, Z = 4, Mr = 550.79, Dc = 2.795 g/cm^3, F(000) = 995, μ(MoKa) = 14.415 mm^-1, 2(MoKa) = 0.71073 A^°, T= 293(2) K, 2θmax = 54.9°, GOOF= 1.053, the final R = 0.0310 and wR = 0.0742 for 2547 observed reflections with I 〉 2σ(I) (refinement on F^2). Complex 1 is connected through hydrogen bonds to give a one-dimensional supramolecular chain structure. Furthermore, π-π interactions are also found between the pyrimidine rings with the center-to-center distances of 3.439(4) and 3.603(4) A^°, so complex 1 expands the chains into a two-dimensional network. 相似文献
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The title compound {[Cu4(OH)4(2,2'-bpy)4(bqdc)]·2ClO4}n 1 (bqdc = 2,2'-biquino- line-4,4'-dicarboxylic acid) has been synthesized by hydrothermal method. Its crystal structure is of triclinic, space group P1 with a = 7.6561(5), b = 12.4652(8), c = 15.7501(10) , α = 80.0480(10), β = 87.7900(10), γ = 74.0800(1)o, V = 1423.65(16) 3, Z = 2, C30H23ClN5O8Cu2, Mr = 744.06, Dc = 1.736 g/cm3, μ = 1.651 mm─1, F(000) = 754, the final R = 0.0421 and wR = 0.1163 for 4973 observed reflections with I > 2σ(I). In 1, tetra-copper chair-like clusters of [Cu4(OH)4(2,2'-bpy)4]4+ are connected by bqdc ligands to form one-dimensional chains, which are further connected by hydrogen bonds to generate a two-dimensional supramolecular network . 相似文献