水热处理参数对Ti6Al4V合金微弧氧化膜HA生成的影响

采用微弧氧化的方法在Ti6Al4V合金表面生成一层富含Ca和P元素的氧化膜,对其进行水热处理,并生成具有生物活性的羟基磷灰石(HA)涂层。研究了处理介质为氨水(pH=10)时,水热处理温度、水热处理时间、冷却条件及填充度对水热处理后钛合金微弧氧化膜表面生成羟基磷灰石的影响。结果表明:随着处理温度和保温时间的延长,HA数量增多,颗粒增大;随釜冷却处理比空冷处理得到的HA更加粗大,并且分布更加均匀致密;填充度增加,HA分布趋于均匀但是形状趋向不规则。

Effects of heat treatment conditions and Y-doping on structure and phase transition temperature of VO2 powders

The VO2 powders were prepared by hydrothermal synthesis.The effects of heat treatment conditions and Y-doping on the structure and phase transition temperature of VO2 were studied.The XRD,SEM and TEM results show that the heat treatment temperature has a significant effect on the crystal transformation of VO2 precursor.Increasing temperature is conducive to the transformation of precursor VO2(B)to ultrafine VO2(M).The Y-doping affects the structure of VO2.Y^3+can occupy the lattice position of V4+to form YVO4 solid solution,which can increase the cell parameters of VO2.Due to the lattice deformation caused by Y-doping,the aggregation of particles is prevented,and the grain is refined obviously.DSC curves show that Y-doping can reduce the phase transition temperature of VO2(M).After adding 9 at.%Y,the phase transition temperature can be reduced from 68.3 to 61.3℃.

Modifying the acidity of H-MOR and its catalytic carbonylation of dimethyl ether

Among the reactions catalyzed by zeolites there are some that exhibit high selectivity due to the spatial confinement effect of the zeolite framework.Tailoring the acidity,particularly the distribution and location of the Bronsted acid sites in the zeolite is effective for making it a better catalyst for these reactions.We prepared a series of H-mordenite（H-MOR） samples by varying the composition of the sol-gel,using different structure directing agents and post-treatment.NH3-TPD and IR characterization of adsorbed pyridine were employed to determine the amount of Bronsted acid sites in the 8-membered ring and 12-membered ring channels.It was shown that controlled synthesis was a promising approach to improve the concentration of Bronsted acid sites in MOR,even with a low Al content.Using an appropriate composition of Si and Al in the sol-gel favored a higher proportion of Bronsted acid sites in the 8-membered ring channels.HMI as a structure-direct agent gave an obvious enrichment of Bronsted acid sites in the 8-membered ring.Carbonylation of dimethyl ether was used as a probe reaction to examine the modification of the acid properties,especially the Bronsted acid sites in the 8-membered ring channels.There was a linear relationship between methyl acetate formation and the number of Bronsted acid sites in the 8-membered ring channels,demonstrating the successful modification of acid properties.Our results provide information for the rational design and modification of zeolites with spatial constraints.

Low-temperature Synthesis of Belite Cement from Reactive Mixtures Based on Coal Fly Ash

This paper summarizes the selected results of an extensive investigation of application of two methods （hydrothermal and mechanochemical） assisted by calcination for synthesizing belite cement from reactive mixtures （CaO/SiO2 molar ratio of 2） consisting of various waste kinds from fluidized brown coal combustion in Slovakian power plant and CaO addition. Based on XRD diffraction patterns and infrared spectra ofpre-treatment products, the formation of the new profiles corresponding to CSH phases with low degree of ordering as belite precursors after hydrothermal treatment as well as metastables calcium silicates and aluminosilicates in mechanosynthesized products was confirmed. Calcination of hydrothermally treated products led to transformation of CSH phases to wollastonite （CS）, belite and gehlenite phase, whereas creation oft^- and I^-C2S or wollastonite in milled reactive mixture took place. Differences in phase composition of products before and after calcination depend upon waste quality and precursor＇s synthesis conditions. Bottom ash isn＇t suitable as raw material for synthesizing belite phase because of high CaO content fixed in anhydrite form （44.1%）. Coal fly ash with low CaO content in anhydrite form （4.2%） and its mechanochemical or hydrothermal treatment in combination with subsequent heating offer opportunities for the utilization of coal fly ash as raw material for belite production.

Influence of Hydrothermal Pre-Treatment of Coal Fly on the Synthesis of Belite Phase

In this paper, the results of an extensive investigation of hydrothermal pre-treatment for synthesizing belite phase from reactive mixtures （CaO/SiO2 molar ratio of 2） consisting of one waste kinds （bottom ash-BA or fly ash-FA） from fluidised brown coal combustion in Slovakian power plant and CaO （analytical grade reagent） addition are summarized. Changes in structure and phase composition of hydrothermally synthesized belite precursors and subsequent calcinated products were compared with those of starting mixtures. Based on XRD diffraction patterns, the formation of the new profiles corresponding to CSH phases with low degree of ordering as belite precursors after hydrothermal treatment was confirmed. Calcination of hydrotermally treated products at 900℃ led to transformation of CSH phases to wollastonite, belite and gehlenite phase. Differences in phase composition of products before and after calcination depend upon waste quality and precursor＇s synthesis conditions. Bottom ash isn＇t suitable as raw material for synthesizing belite phase because of high CaO content fixed in anhydrite form （44.1%）. Coal fly ash with low CaO content in anhydrite form （4.2%） and its hydrothermal treatment in combination with subsequent heating offer opportunities for the utilization of coal fly ash as raw material for belite production.