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31.
On the Hydrates M(HSeO3)2 · 4H2O (M = Mg, Co, Ni, Zn) – Crystal Structures, IR, Raman, and Thermoanalytical Investigations From aqueous solutions of M(HSeO3)2 single crystals of Mg(HSeO3)2 · 4H2O and of the hitherto unknown compounds Co(HSeO3)2 · 4H2O, Ni(HSeO3)2 · 4H2O and Zn(HSeO3)2 · 4H2O could be obtained. The crystal structures, X-ray powder, IR, Raman and thermoanalytical (DTA, TG, Raman heating) data are presented and discussed. The crystal data of the isotypic compounds are: monoclinic, space group C2/c, Z = 4, Mg: a = 1 464.6(2), b = 755.3(1), c = 1 099.9(1) pm, β = 126.59(1)°, V = 0.9769(1) nm3, Co: a = 1 462.5(2), b = 756.5(2), c = 1 102.2(2) pm, β = 126.53(1)°, V = 0.9798(2) nm3, Ni: a = 1 452.2(2), b = 751.0(1), c = 1 091.5(1) pm, β = 126.28(1)°, V = 0.9595(1) nm3, Zn: a = 1 468.3(2), b = 755.8(1), c = 1 103.1(1) pm, β = 126.79(1)°, V = 0.9804(2) nm3. The crystal structures consist of hexagonal packed [M(HSeO3)2 · 2H2O]n chains of [MO4(H2O)2] octahedra linked by Se atoms. They contain trigonal pyramidal SeO2OH?ions with “free” hydroxyl groups and also “free” molecules of water of crystallization. The hydroxyl groups build strong H-bonds (O? H …? O distances: 265–268 pm). The IR spectra show AB doublett bands in the OH stretching mode region of the hydroxyl groups. The water molecules of crystallization are linked to planar (H2O)4 tetramers by H-bonds with unusually short O? H …? O bond distances of 271–273 pm. DTA and TG measurements indicate that thermal decomposition results in the direct formation of the respective diselenite MSe2O5. Raman heating measurements show under quasi static conditions the intermediate formation of the anhydrous hydrogen selenites. 相似文献
32.
杂原子Y分子筛的二次合成及其吸附脱硫性能 总被引:13,自引:0,他引:13
采用液-固相同晶取代反应制备了骨架含Ga的Y型分子筛, 并对其吸附脱硫性能进行了研究. 在室温, 空速为7 h−1的条件下, 镓化Y型分子筛([Ga]AlY)处理噻吩、四氢噻吩、4,6-二甲基二苯并噻吩(4,6-DMDBT)正壬烷溶液(硫含量500 μg•g−1), 每克吸附剂吸附硫的量分别为7.7、17.4、14.5 mg. 采用密度泛函理论(DFT)中的广义梯度近似方法(GGA)计算各分子中硫原子上的电荷数, 噻吩中硫原子的电荷数为−0.159, 而4,6-DMDBT和四氢噻吩分别为−0.214、0.298. 四氢噻吩和4, 6-DMDBT中硫原子上的电子密度大于噻吩中硫原子上的电子密度, 这就使得四氢噻吩和4,6-DMDBT中的硫原子与吸附位间的作用会远大于噻吩中的硫原子与吸附位间的作用, 吸附容量必然会大很多. 采用[Ga]AlY处理抚顺石油二厂的催化裂化汽油(硫含量:299 μg•g−1), 每克吸附剂处理2.1 mL汽油时, 处理后汽油的硫含量为54.8 μg•g−1, 说明[Ga]AlY对汽油脱硫有一定的效果. 相似文献
33.
Pyrolysis and TG Analysis of Shivee Ovoo Coal from Mongolia 总被引:2,自引:0,他引:2
B. Avid B. Purevsuren M. Born J. Dugarjav Ya. Davaajav A. Tuvshinjargal 《Journal of Thermal Analysis and Calorimetry》2002,68(3):877-885
The coal sample of the Shivee Ovoo deposits has been non-isothermally pyrolysed in a thermogravimetric analyser to determine
the influence of temperature, heating rate and purge gas employed on the thermal degradation of the sample. The heating rates
investigated in the TG were 10–50 K min–1 to final temperature of 1000°C. N2or CO2 were employed as well as type of purge gas on the process of thermal degradation of the coal sample. The coal was also investigated
in a fixed bed reactor to determine the influence of temperature and heating rate of the pyrolysis on the yield of products
and composition of the gases evolved. The main gases produced were H2, CH4, C2H2, C2H4, C2H6, C3H6 and C3H8 and also minor concentrations of other gases.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
34.
This research was aimed
to investigate the role of clay on the combustion and kinetic behavior of
crude oils in limestone matrix. For this purpose, simultaneous TG (thermogravimetry)
and DTA (differential thermal analysis) experiments were performed at three
different heating rates as 10–15 and 20°C min–1,
respectively. A uniform trend of decreasing activation energies was observed
with the addition of clay. It was concluded that clays surface area affects
the values of Arrhenius constant, while it is the catalytic properties of
clay, which lower the activation energies of all the reactions, involved in
the combustion process. 相似文献
35.
微波消解凯氏定氮法快速测定酱油中全氮 总被引:1,自引:0,他引:1
研究了凯氏定氮法测定酱油中全氮时样品的微波消解方法,进行了微波消解条件的选择及消解结果精密度试验,并与国家标准方法对比,验证了方法的准确度。试验结果表明,消解完全仪需20min,相对标准偏差均小于2%(n=7),回收率范围为96%~103%,经t检验,微波溶样法与国家标准凯氏定氮法的测定结果无显著性差异。 相似文献
36.
Karim Adil Gilles Dujardin Marc Leblanc Vincent Maisonneuve 《Journal of fluorine chemistry》2004,125(11):1709-1714
Tren amine cations and carbonate anions adopt a ternary symmetry while tetra amine cations are tetrahedral. The symmetry of these constitutive ions influences strongly the nature of the solids which crystallise from solutions. Large fluorinated aluminate polyanions with tetrahedral symmetry appear in the presence of tren amine, while infinite chains of AlF6 octahedra are observed with tetra amine and that noncentrosymmetric structures are frequently encountered in rare earth fluoride carbonates. 相似文献
37.
Dilatometry is a technique for precise measurement of thermal dilatation of materials during heating or cooling. A procedure has been presented for calibration of a differential dilatometer operating with electromagnetic heating for metallic specimens both upon heating and cooling as well as under uniaxial compressive and tensile loading. The dilation signal has been calibrated for both heating and cooling and for uniaxial loading (compressive and tensile) using platinum or iron reference specimens, for which recommended dilational data are available. The ferro- to paramagnetic transition (characterised by the Curie temperature) of pure iron or iron-based alloys has been adopted to calibrate the temperature in the dilatometric measurement under different loading modes during heating and cooling. On this basis calibrated data for the thermal expansion coefficients of Fe and Fe-Ni alloys have been obtained. 相似文献
38.
为了研究从简单易得的原料在无催化剂的条件下一锅法合成N-甲基十氢吖啶-1,8-二酮化合物,我们以各类醛(脂肪醛、芳香醛、二醛)、达咪酮或1,3-环己二酮和甲胺为原料,以乙二醇或水为溶剂,经微波辐射,一步反应得到了一系列N-甲基十氢吖啶-1,8-二酮化合物。反应时间从传统热反应的4-5小时缩短至2-10分钟,产率较高(56-95%),并且不需要使用催化剂。该反应后处理方便,只需要简单洗涤,环境友好,为合成此类化合物提供了一种简便、有效的合成方法。该方法不仅适用于一元脂肪醛、芳香醛,还适用于芳香二醛,因此可以合成含有一个或两个十氢吖啶结构单元的杂环化合物。 相似文献
39.
A. Davoodnia M. Roshani E. Saleh Nadim M. Bakavoli N. Tavakoli Hoseini 《中国化学快报》2007,18(11):1327-1330
Microwave-assisted synthesis of new 2-arylpyrimido[4′,5′:4,5]thiazolo[3,2-α]benzimidazol-4(3H)-ones from 3-aminothia- zolo[3,2-α]benzimidazol-2-earboxamide and aroyl halides in solvent-free condition is described. In comparison with classical conditions the reactions are faster and the yields are higher under microwave irradiation. 相似文献
40.