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41.
Summary A program is described which calculates the number of effective plates and the coating efficiency over the entire range of a test chromatogram. The peak widths at half height are derived by assuming a Gaussian peak shape. The interpolated peak width at k=4 is used for computing a standardized number of effective plates. Plate height, column permeability, overall performance and a novel parameter called sampling efficiency are calculated from 5 other figures — i. e. carrier gas code, pressure drop, column length, column temperature and particle size.Dedicated to Dr. Leslie S. Ettre for his 60th birthday. 相似文献
42.
A novel series of the formula NdSrNi1−xCuxO4−δ were synthesized for various values of x ranging from 0 to 1 in 1 atm of O2 gas flow using conventional solid-state methods and were characterized by powder X-ray diffraction and electrical resistivity measurements. The compounds have been shown to adopt the K2NiF4-type structure. The oxygen stoichiometry of the compounds was determined from thermo-gravimetric analysis (TGA). An analysis of the micro-structure of the neodymium strontium nickel copper oxide is described. All the samples were semi-conducting from room temperature down to 77 K. The effect of Cu2+ incorporation on the structural and electrical properties of NdSrNi1−xCuxO4−δ, 0?x?1, are discussed in terms of Jahn-Teller distortion of the (Ni/Cu)O6 octahedra and mixed valence character of copper. 相似文献
43.
便携式微波等离子体离子化检测器气相色谱仪用于气体分析的研究 总被引:2,自引:0,他引:2
本文使用自制的便携式微波诱导等离子体离子化检测器气相色谱仪对可燃气体中N_2、O_2、H_2和CH_4的测定方法进行了研究。以氩气为载气和工作气体,考察了改进后的微波诱导等离子体离子化检洲器(MIPID)的工作参数对测定的影响。对煤气和乙炔中的O_2、N_2、H_2和CH_4进行了测定,分析结果与热导池检测器(TCD)的气相色谱法一致。讨论了高电离电位(>11.7ev)气体组分在MIPID中响应特性。 相似文献
44.
《Electroanalysis》2005,17(11):1003-1007
A novel PVC membrane ion‐selective electrode based on tribenzyltin(IV) dithiocarbamate [Sn(IV)–TBDTB] as neutral carrier was developed for thiocyanate (SCN?) determination. The electrode exhibits a near‐Nernstian response for SCN? with a slope of 62.8±2.0 mV per decade over a wide concentration range 1.0×10?1–2.0×10?6 mol L?1 and a detection limit of 1.0×10?6 mol L?1 in MES–NaOH buffer, pH 6.0, at 25 °C. The electrode prepared with 1.5 wt.% Sn(IV)–TBDTB, 32.5 wt.% PVC and 66.0 wt.% 2‐nitrophenyloctyl ether (o‐NPOE) shows optimal response characteristics. Anti‐Hofmeister selectivity sequence for a series of anions shown by the electrode was as follows: SCN?>Sal?>I?>ClO >phCOO?>CH3COO?>Br?>Cl?>NO >NO >Citrate>SO42?. The useful pH range for the electrode was found to be 3–7 with a response time 30–40 s. The electrode has been used for direct determination of thiocyanate in wastewater with satisfactory results. 相似文献
45.
K. Grob 《Journal of separation science》1980,3(6):286-290
The sensitivity of an FID may change when the carrier gas flow rate changes during a chromatographic run. Sample parts which are eluted at reduced FID sensitivity produce a reduced peak area, hence are discriminated as compared to other components. Sensitivity changes were studied for hydrogen as carrier gas. For the detector tested, differences in the carrier gas flow rates of 1 ml/min shifted the FID sensitivity by 1 to 5% (depending on the fuel gas supply). Thus the stability of the sensitivity is no longer ensured as soon as the carrier gas flow rate is changed manually or by an automatic programmer during an analysis. Sensitivity drifts may also occur during temperature programmed runs with a pressure regulated carrier gas supply since the gas flow through the capillary drops with increasing temperature. Such shifts in the response became noticeable as soon as relatively high carrier gas flow rates combined with long range temperature programmes were used. The typical patterns of such discriminations are shown, closing with a discussion on the possibilities for minimizing such undesired effects. 相似文献
46.
A. G. Bubnov E. Yu. Burova V. I. Grinevich V. V. Rybkin J.-K. Kim H.-S. Choi 《Plasma Chemistry and Plasma Processing》2006,26(1):19-30
This study investigated the processes for the destruction of phenol and its derivatives (resorcin and pyrocatechol) in aqueous
solutions under the action of an oxygen dielectric barrier discharge (DBD) at atmospheric pressure in the presence or absence
of catalysts in the plasma zone. It was shown that the DBD had a high decomposition efficiency for phenol and its derivatives
(up to 99%). Phenol was the most stable and pyrocatechol was the least. In a plasma-catalytic hybrid process, the effective
rate constants for phenol, resorcin and pyrocatechol decomposition were 11, 4 and 2.5 times higher, respectively, than those
for the DBD treatment without catalysts. The process also resulted in a 1.4, 1.6 and 1.2 times higher rate of carboxylic acid
formation for phenol, resorcin and pyrocatechol, respectively. The fractional conversion into the respective carboxylic acids
reached 56% for phenol and 68% for resorcin and pyrocatechol. 相似文献
47.
Three new cobalt complexes were synthesized by solid-state reaction at room temperature. It was found that one mole of complex reacted with two moles of oxygen at room temperature. And the oxygenated complexes [Co·(L1)2·2O2](NO3)2·2H2O (L1=N,N′-bis(4-hydroxyl-3-methoxy-benzyl)-triethylenetetramine), [Co·(L2)2·2O2](NO3)2 ·2H2O (L2=N,N′-bis(4-hydroxyl-benzyl)-triethylenetetramine) and [Co·L3·2O2](NO3)2·2H2O (L3=N,N′-bis(2-hydroxyl-benzyl)-triethylenetetramine) were obtained and characterized by elemental analysis, IR spectra, 1H NMR, TG/DTA, UV-Vis and molar conductance. The coordinated oxygen contents in the oxygenated complex were also determined by weight method. It was found that one O2 molecule coordinated to the Co ion and formed superoxo type oxygenated complex. 相似文献
48.
E.?BertoloEmail author J.?A.?Kilner M.?Sahibzada 《Journal of Solid State Electrochemistry》2004,8(9):585-591
18O/16O isotope exchange depth profiling (IEDP) combined with secondary ion mass spectrometry (SIMS) has been used to measure the oxygen tracer diffusivity of SrCe0.95Yb0.05O3– between 800 °C and 500 °C at a nominal pressure of 200 mbar. The values of D* (oxygen tracer diffusion coefficient) and k (surface exchange coefficient) increase steadily with increasing temperature, and the activation energies are 1.13 eV and 0.96 eV, respectively. Oxygen ion conductivities have been calculated using the Nernst–Einstein equation. The transport number for oxide ions at 769 °C, the highest temperature studied, is only ~0.05. Moreover, SrCe0.95Yb0.05O3– has been studied using impedance spectroscopy under dry O2, wet O2 and wet H2 (N2/10% H2) atmospheres, over the range 850–300 °C. Above ~550 °C, SrCe0.95Yb0.05O3– shows higher conductivity in dry O2 than in wet O2 or wet H2; below that temperature the results obtained for the three atmospheres are comparable. Dry O2 shows the highest activation energy (0.77 eV); the activation energies for wet O2 and wet H2 are identical (0.62 eV).Abbreviations HTPC high-temperature proton conductor - IEDP isotope exchange depth profiling - SIMS secondary ion mass spectrometryPresented at the OSSEP Workshop Ionic and Mixed Conductors: Methods and Processes, Aveiro, Portugal, 10–12 April 2003 相似文献
49.
Oxygen is electroreduced to water on a carbon cathode coated with wired bilirubin oxidase in a pH 7.4 0.15 M NaCl phosphate buffer solution at 37 °C at much lesser polarization than it is on a pure platinum cathode in 0.5 M H2SO4. While the wired bilirubin oxidase cathode operates for over a week in the aerated or oxygenated buffer solution, it is degraded rapidly when in serum. We reported earlier that in the presence of O2 an intermediate product of the electrooxidation of urate, which is a normal serum component, irreversibly damages the wired bilirubin oxidase and also reported that the electrocatalyst is irreversibly damaged, in the absence of urate, when it is brought, by disconnecting the electrode, to the O2/H2O half cell potential at pH 7.4. Here we report that a) dissolved bilirubin oxidase is irreversibly and rapidly damaged by urate in the presence of O2; and b) that the immobilized wired bilirubin oxidase electrocatalyst is not only irreversibly deactivated by urate in the presence of O2 in a few hours, but is initially reversibly deactivated, in 1 min or less, by the urate in the presence of O2. 相似文献
50.
Sodium-dicyclohexyl- 18-crown-6 complex cation was used as carrier for the uphill transport of zinc as Zn(SCN)42? complex anion. By using L-cysteine as a metal ion acceptor in the receiving phase at the optimized pH of 7.6, the amount of zinc transport through the liquid membrane after 90 min was 97.2 ± 1.0%. The selectivity and efficiency of zinc transport from aqueous solutions containing equimolar mixtures of Ag+, Cd2+ Co2+, Cu2+, Fe2+, Ni2+, Pb2+, Pd2+, Sr2+, Bi3+, Cr3+ and Fe3+ ions was investigated. In the presence of NH2OH.HCl as a suitable masking agent in the source phase, the interfering effect of Cu2+ and Pb2+ ions was diminished drastically. 相似文献