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71.
Dr. Bodo Hattendorf Bianca Gusmini Dr. Ladina Dorta Prof. Dr. Robert S. Houk Prof. Dr. Detlef Günther 《Chemphyschem》2016,17(17):2640-2644
Doubly charged diatomic ions MAr2+ where M=Mg, Ca, Sr or Ba have been observed by mass spectrometry with an inductively coupled plasma ion source. Abundance ratios are quite high, 0.1 % for MgAr2+, 0.4 % for CaAr2+, 0.2 % for SrAr2+ and 0.1 % for BaAr2+ relative to the corresponding doubly charged atomic ions M2+. It is assumed that these molecular ions are formed through reactions of the doubly charged metal ions with neutral argon atoms within the ion source. Bond dissociation energies (D0) were calculated and agree well with previously published values. The abundance ratios MAr+/M+ and MAr2+/M2+ generally follow the predicted bond dissociation energies with the exception of MgAr2+. Mg2+ should form the strongest bond with Ar [D0 (MgAr2+)=124 to 130 kJ mol?1] but its relative abundance is similar to that of the weakest bound BaAr2+ (D0=34 to 42 kJ mol?1). The relative abundances of the various MAr2+ ions are higher than those expected from an argon plasma at T=6000 K, indicating that collisions during ion extraction reduce the abundance of the MAr2+ ions relative to the composition in the source. The corresponding singly charged MAr+ ions are also observed but occur at about three orders of magnitude lower intensity than MAr2+. 相似文献
72.
Dr. Ines E. Collings Dr. Elena Bykova Dr. Maxim Bykov Dr. Sylvain Petitgirard Dr. Michael Hanfland Dr. Damian Paliwoda Prof. Leonid Dubrovinsky Prof. Natalia Dubrovinskaia 《Chemphyschem》2016,17(21):3369-3372
The incorporation of noble gas atoms, in particular neon, into the pores of network structures is very challenging due to the weak interactions they experience with the network solid. Using high‐pressure single‐crystal X‐ray diffraction, we demonstrate that neon atoms enter into the extended network of ammonium metal formates, thus forming compounds Nex[NH4][M(HCOO)3]. This phenomenon modifies the compressional and structural behaviours of the ammonium metal formates under pressure. The neon atoms can be clearly localised within the centre of [M(HCOO)3]5 cages and the total saturation of this site is achieved after ~1.5 GPa. We find that by using argon as the pressure‐transmitting medium, the inclusion inside [NH4][M(HCOO)3] is inhibited due to the larger size of the argon. This study illustrates the size selectivity of [NH4][M(HCOO)3] compounds between neon and argon insertion under pressure, and the effect of inclusion on the high‐pressure behaviour of neon‐bearing ammonium metal formates. 相似文献
73.
Vilma Petkova Y. Pelovski I. Dombalov Kaia Tánsuaadu 《Journal of Thermal Analysis and Calorimetry》2005,80(3):701-708
Summary The free energy of the acidic ammonium sulfate is a good precondition its use as an additive or reagent for decomposition of natural phosphates on the way to obtain NPS or NPKS complex fertilizers. During our previous studies it was confirmed that as a result of thermo-mechanical treatment new solid phases are formed as a result of the phosphates decomposition. The aim of this study is to find out appropriate conditions for thermal treatment of Tunisia phosphorite with ammonium sulfate where the content of P2O5 soluble forms has its maximum. The process was investigated under dynamic thermal conditions. Structure and phase transformations of the mixtures to intermediate and final solid products are confirmed by different techniques. X-ray powder diffraction, infrared spectroscopy and electron microscopy have been applied successfully and relationship found between phase structure and thermal treatment applied. As a result of the complex studies optimal temperatures are determined. The solid products under optimal conditions contain phosphorous in soluble forms available for plants in the soil. As a final it is concluded that the final products could be used as complex mineral fertilizers. 相似文献
74.
采用强流相对论电子束横向泵浦纯氩,获得了属于Ar的第三谱带范围内240nm中心谱区的光强随气压变化的关系.结果表明,压强为3×105Pa时是产生这一谱区的最佳气压,并证实了这一谱区是由带电的原子团簇产生的. 相似文献
75.
The standard enthalpies of solution of rare gases (helium, neon, argon, krypton, and xenon) in water at 25°C have been measured by a high precision steady-state calorimetric method. The aqueous solvation process is energetically favorable at 25°C for the gases studied. Values of the standard free energy, enthalpy, and entropy changes are found to be well correlated with cavity surface areas and the number of water molecules in the first solvation shell. Also, the values of the standard enthalpy and entropy of solution for the rare gases are found to have the same dependence on the number of solvation shell water molecules as inorganic and hydrocarbon gases. These results imply that the dominant source of enthalpy and entropy change resides in the first solvation shell. 相似文献
76.
Enzymatic reactions in supercritical gases 总被引:10,自引:0,他引:10
D. A. Hammond M. Karel A. M. Klibanov V. J. Krukonis 《Applied biochemistry and biotechnology》1985,11(5):393-400
The enzyme polyphenol oxidase has been found to be catalytically active in supercritical carbon dioxide and fluoroform: it
readily oxidizesp-cresol andp-chlorophenol to their correspondingo-benzoquinones. 相似文献
77.
Bernard Lavielle Bertrand Thomas Eric Gilabert Gregory Canchel Denis Horlait Sylvain Topin Fabien Pointurier Christophe Moulin 《Journal of mass spectrometry : JMS》2016,51(10):908-913
A double focusing sector field mass filter used in Nier–Johnson geometry has been built in order to perform Kr isotope enrichment for 81Kr and 85Kr isotopes. The principle consists in implanting Kr+ ions accelerated at 7 keV in Al foils after separation using the magnetic sector. A specific ion source has been designed capable of generating high Kr+ ion beams (>0.5 μA) to transfer into the collecting Al foils in 3 to 5 h significant fractions of large Kr samples (1015 to 1016 atoms) initially introduced in the instrument. Implanted Kr isotopes can be further selectively released from the Al foil by surface ablation using an infrared laser beam. Implantation yields and enrichment factors are measured using a conventional mass spectrometer. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
78.
C. A. Rinaldi J. C. Ferrero S. I. Lane E. V. Oexler 《Journal of Chemical Sciences》1991,103(3):465-469
The IR multiphoton dissociation of CF3I has been studied in the presence of isobutane and with isobutane and Ar and CO2 as inert gases. The dependence of the reaction probability P(Φ) with fluence (ϕ) is confirmed. Modeling of the experimental results shows that for the energy transfer processes the average energy transferred
per collision 〈†E〉d varies with (ϕ). 相似文献
79.
After describing simplified equations exspressing the temparature dependency of the viscosity of carrier gases (helium, nitrogen and hydrogen ) relative to a base value, absolute relationships based on the kinetic theory of gases are discussed. Comparative data obtained using various calculation methods are given and are compared to measured values. Based on the kinetic relationshipsm, of viscosity. Finally, the influence of pressure on the viscosity is also briefly discussed. As a supplement, Viscosity data are tabulated for the three gases in the range of 0°C to 400°C in increments of 2 K, calculated using the kinetic relationships. 相似文献
80.
A new infrared-spectroscopic method to characterize acid sites of zeolites using small and weakly basic molecules such as diatomic and monoatomic molecules is reviewed. It has been revealed that N2 is an effective probe molecule to characterize both Brønsted acidity and Lewis acidity of H-form zeolites. The characteristics of the N 2 probe are discussed in detail in comparison with the CO probe. O2 and rare gases have also been applied to monitor the strong acid sites in the H-form zeolites. Further, the studies of the adsorption of water on H-form zeolites are shortly reviewed: a recent IR study of the H2
18O adsorption on H-ZSM-5 has given direct experimental evidence that the main feature of the observed IR bands is due to the hydrogen-bonded adsorption of water on the Brønsted acid sites. 相似文献