Manipulation and Separation of Particles of Metal Oxides by Dielectrophoresis

With the development of nanotecbnology, the separation and manipulation of micro-nano-panicles have become a research focus in the field of nano-materials, nielectrophoresis（DEP） is a non-contact technology for the separation and manipulation of micro-nano-particles. Here is reported the design and fabrication of a DEP based microchip with microelectrode arrays for capturing micro-particles of inorganic oxides in petroleum. The DEP behavior of micro-particles of inorganic oxides in oil media was explored via this microchip. The microchip shows relatively a good DEP response to inorganic oxides in oil media. Furthermore, much more factors were explored such as fiequency（Hz）, and particle size（μm）, as well as metal valence. As a conclusion, the best frequency is 50 Hz. It is expected to capture panicles with different sizes or separate different oxide panicles by regulating DEP conditions. Thus, a new method could be established for the separation and purification panicles of different oxides, as well as the separation and manipulation of an oxide with different particle sizes.

Role of secondary aerosols in haze formation in summer in the Megacity Beijing

A field experiment from 18 August to 8 September 2006 in Beijing, China, was carried out. A hazy day was defined as visibility 〈 10 km and RH（relative humidity） 〈 90%. Four haze episodes, which accounted for ～ 60% of the time during the whole campaign, were characterized by increases of SNA（sulfate, nitrate, and ammonium） and SOA（secondary organic aerosol） concentrations. The average values with standard deviation of SO2-＋4, NO-3, NH4 and SOA were 49.8（± 31.6）, 31.4（±22.3）, 25.8（±16.6） and 8.9（±4.1） μg/m3, respectively, during the haze episodes, which were 4.3, 3.4, 4.1, and 1.7 times those in the non-haze days. The SO2-4,NO-3, NH＋4, and SOA accounted for 15.8%, 8.8%, 7.3%, and 6.0% of the total mass concentration of PM10 during the non-haze days. The respective contributions of SNA species to PM10 rose to about27.2%, 15.9%, and 13.9% during the haze days, while the contributions of SOA maintained the same level with a slight decrease to about 4.9%. The observed mass concentrations of SNA and SOA increased with the increase of PM10 mass concentration, however, the rate of increase of SNA was much faster than that of the SOA. The SOR（sulfur oxidation ratio） and NOR（nitrogen oxidation ratio） increased from non-haze days to hazy days, and increased with the increase of RH. High concentrations of aerosols and water vapor favored the conversion of SO2 to SO2-4and NO2 to NO-3, which accelerated the accumulation of the aerosols and resulted in the formation of haze in Beijing.