NaH doped TiO_(2)as a high-performance catalyst for Mg/MgH_(2)cycling stability and room temperature absorption

This paper presents the catalytic effect of NaH doped nanocrystalline TiO_(2)(designated as NaTiOxH)in the improvement of MgH_(2)hydrogen storage properties.The catalyst preparation involves ball milling NaH with TiO_(2)for 3 hr.The addition of 5 wt%NaTiOxH powder into MgH_(2)reduces its operating temperature to∼185℃,which is∼110℃lower than the additive-free as-milled MgH_(2).The composite remarkably desorbs∼7.2 wt%H_(2)within 15 min at∼290℃and reabsorbs∼4.5 wt%H_(2)in 45 min at room temperature under 50 bar H_(2).MgH_(2)dehydrogenation is activated at 57 kJ/mol by the catalyst.More importantly,the addition of 2.5 wt%NaTiOxH catalyst aids MgH_(2)to reversibly produce∼6.1 wt%H_(2)upon 100 cycles within 475 hr at 300℃.Microstructural investigation into the catalyzed MgH_(2)composite reveals a firm contact existing between NaTiOxH and MgH_(2)particles.Meanwhile,the NaTiOxH catalyst consists of catalytically active Ti_(3)O_(5),and“rod-like”Na_(2)Ti_(3)O_(7)species liberated in-situ during preparation;these active species could provide multiple hydrogen diffusion pathways for an improved MgH_(2)sorption process.Furthermore,the elemental characterization identifies the reduced valence states of titanium(Ti<4+)which show some sort of reversibility consistent with H_(2)insertion and removal.This phenomenon is believed to enhance the mobility of Mg/MgH_(2)electrons by the creation and elimination of oxygen vacancies in the defective(TiO_(2-x))catalyst.Our findings have therefore moved MgH_(2)closer to practical applications.

Low temperature laser absorption spectra of methane in the near-infrared at 1.65 μm for lower state energy determination

Direct absorption spectra of the 2v3 band of methane （CH4） from 6038 to 6050 cm 1 were studied at different low temperatures using a newly developed cryogenic cell in combination with a distributed feedback （DFB） diode laser. The cryogenic cell can operate at any stabilized temperature ranging from room temperature down to 100 K with temperature fluctuation less than =t=1 K within 1 hour. In the present work, the CH4 spectra in the range of 6038-6050 cm-1 were recorded at 296, 266, 248, 223, 198, and 176 K. The lower state energy Ett and the rotational assignment of the angular momentum J were determined by a ＂2-low-temperature spectra method＂ using the spectra recorded at 198 and 176 K. The results were compared with the data from the GOSAT and the recently reported results from Campargue and co-workers using two spectra measured at room temperature and 81 K. We demonstrated that the use of a 2-low-temperature spectra method permits one to complete the Ett and J values missed in the previous studies.

Determination of Impurity Silicon in Anticancer Drug (Ge-132) by Electrothermally Atomised Atomic Absorption Spectrometry with Optical Temperature Control Accessory

The present paper describes the ashing and atomization processes in silicon analysis by electrothermally atomised atomic absorption spectrometry(EAAAS) with an uncoat-ed graphite tube, a pyrolytically coated graphite tube and a tungsten-coated graphitetube. The sensitivity and linear range of three graphite tubes were compared. By using optical temperature control accessory, the signals are enhanced by a factor of 2 and the germanium interferences in the determination of silicon are eliminated. The effects of time constant and carrier gas flow-rate on the determination of silicon were also tested. The sample can be directly analyzed in its aqueous solution without any pretreatment. The measurements of samples containing 0. 2 μg/mL and 0. 4 μg/mL silicon were run ten times and the variation coefficient is 4. 9% and 2.6%, respectively. The recovery tests for carboxyethyl germanium sesquioxide(Ge-132) synthesized and imported were performed, and the recoveries are 97. 0% and 110%, respectively. Keywords Carboxyethyl germanium sesquioxide, Electrothermally atomised atomic absorption spectrometry, Silicon

Hydrogen absorption of LaFe_(11.5)Si_(1.5) compound under low hydrogen gas pressure

Hydrogen absorptions of LaFe11.sSi1.5 compound in 1-atm hydrogen gas at different temperatures are investigated. The hydrogen content in the hydrogenated sample does not increase with the increase of temperature of hydrogen absorption but changes complicatedly. The characteristic of first-order transition in LaFe11.sSil.5 compound is weakened after hydrogen absorption. It leads the peaks of magnetic entropy to become wider and the hysteresis loss to reduce significantly, but relative cooling power （RCP） is not changed considerably.

Encapsulation of 2-amino-2-methyl-l-propanol with tetraethyl orthosilicate for C02 capture

Carbon capture is widely recognised as an essential strategy to meet global goals for climate protection.Although various C02 capture technologies including absorption,adsorption and membrane exist,they are not yet mature for post-combustion power plants mainly due to high energy penalty.Hence researchers are concentrating on developing non-aqueous solvents like ionic liquids,C 02-binding organic liquids,nanoparticle hybrid materials and microencapsulated sorbents to minimize the energy consumption for carbon capture.This research aims to develop a novel and efficient approach by encapsulating sorbents to capture C02 in a cold environment.The conventional emulsion technique was selected for the microcapsule formulation by using 2-amino-2-methyl-l-propanol(AMP)as the core sorbent and silicon dioxide as the shell.This paper reports the findings on the formulated microcapsules including key formulation parameters,microstructure,size distribution and thermal cycling stability.Furthermore,the effects of microcapsule quality and absorption temperature on the C02 loading capacity of the microcapsules were investigated using a self-developed pressure decay method.The preliminary results have shown that the AMP microcapsules are promising to replace conventional sorbents.