Novel sensor selection strategy for LPI based on an improved IMMPF tracking method

Sensor platforms with active sensing equipment such as radar may betray their existence, by emitting energy that will be intercepted by enemy surveillance sensors. The radar with less emission has more excellent performance of the low probability of intercept（LPI）. In order to reduce the emission times of the radar, a novel sensor selection strategy based on an improved interacting multiple model particle filter（IMMPF） tracking method is presented. Firstly the IMMPF tracking method is improved by increasing the weight of the particle which is close to the system state and updating the model probability of every particle. Then a sensor selection approach for LPI takes use of both the target＇s maneuverability and the state＇s uncertainty to decide the radar＇s radiation time. The radar will work only when the target＇s maneuverability and the state＇s uncertainty exceed the control capability of the passive sensors. Tracking accuracy and LPI performance are demonstrated in the Monte Carlo simulations.

Effects of SO2 and H2O on low-temperature NO conversion over F-V2O5-WO3/TiO2 catalysts

F-V2 O5-WO3/Ti02 catalysts were prepared by the impregnation method.As the content of F ions increased from 0.00 to 0.35 wt.%,the NO conversion of F-V2 O5-WO3/TiO2 catalysts initially increased and then decreased.The 0.2 F-V2 O5-WO3/TiO2 catalyst(0.2 wt.%F ion)exhibited the best denitration(De-NOx)performance,with more than 95%NO conversion in the temperature range 160-360℃,and 99.0%N2 selectivity between 110 and 280℃.The addition of an appropriate amount of F ions eroded the surface morphology of the catalyst and reduced its grain size,thus enhancing the NO conversion at low temperature as well as the sulfur and water resistance of the V2 O5-WO3/Ti02 catalyst.After selective catalytic reduction(SCR)reaction in a gas flow containing SO2 and H2 O,the number of NH3 adsorption sites,active component content,specific surface area and pore volume decreased to different degrees.Ammonium sulfate species deposited on the catalyst surface,which blocked part of the active sites and reduced the NO conversion performance of the catalyst.On-line thermal regeneration could not completely recover the catalyst activity,although it prolonged the cumulative life of the catalyst.In addition,a mechanism for the effects of S02 and H2 O on catalyst NO conversion was proposed.

NH_3-SCR denitration catalyst performance over vanadium–titanium with the addition of Ce and Sb

Selective catalytic reduction technology using NH3 as a reducing agent（NH3-SCR） is an effective control method to remove nitrogen oxides. TiO2-supported vanadium oxide catalysts with different levels of Ce and Sb modification were prepared by an impregnation method and were characterized by X-ray diffractometer（XRD）, Brunauer-Emmett-Teller（BET）, Transmission electron microscopy（TEM）, Fourier transform infrared spectroscopy（FT-IR）, UV-Vis diffuse reflectance spectroscopy（UV-Vis DRS）, Raman and Hydrogen temperature-programmed reduction（H2-TPR）. The catalytic activities of V5 CexS by/TiO2 catalysts for denitration were investigated in a fixed bed flow microreactor. The results showed that cerium, vanadium and antimony oxide as the active components were well dispersed on TiO2, and the catalysts exhibited a large number of d-d electronic transitions, which were helpful to strengthen SCR reactivity. The V5 CexS by/TiO2 catalysts exhibited a good low temperature NH3-SCR catalytic activity. In the temperature range of 210 to 400℃, the V5 CexS by/TiO2 catalysts gave NO conversion rates above 90%. For the best V5Ce35Sb2/TiO2 catalyst, at a reaction temperature of 210℃, the NO conversion rate had already reached 90%. The catalysts had different catalytic activity with different Ce loadings. With the increase of Ce loading, the NO conversion rate also increased.