Effect of H_2O on NO Reduction over NSR Catalyst 12CaO·7Al_2O_3/10%K

A novel NOx storage/reductiou catalyst 12CaO·7Al2O3/10%K, defined as C12A7/K, was prepared, which possesses good NOx storage/reduction ability with a high sulfur-tolerance. The effect of H2O on the NO reduction features over the C12A7/K catalyst was investigated, The NO eonversion and the N2 selectivity were measured as a function of temperature and H2O concentration. In the presence of 1.2% H2O, both the NO conversion and the N2 selectivity significantly decrease at lower temperature region （〈500 ℃）. At temperatures over 500℃, however, the NO reduction is only slightly influenced by H2O, The species of NO3^-/NO2^- are confirmed as main storage components in the C12A7/K catalyst, which are thrther reduced into N2 by H2 under the reduction conditions.

The effect of cations(NH_4^+,Na^+,K^+,and Ca^(2+)) on chemical deactivation of commercial SCR catalyst by bromides

Alkali and alkaline‐earth metals from fly ash have a significant deactivation effect on catalysts used for selective catalytic reduction of NOx by NH3(NH3‐SCR).Bromides are considered effective additives to improve Hg0 oxidation on SCR catalysts.In this work,the effects of different bromides(NH4Br,NaBr,KBr,and CaBr2)on a commercial V2O5‐WO3/TiO2 catalyst were studied.NOx conversion decreased significantly over the KBr‐poisoned catalyst(denoted as L‐KBr),while that over NaBr‐and CaBr2‐poisoned catalysts(denoted as L‐NaBr and L‐CaBr,respectivity)decreased to a lesser extent compared with the fresh sample.Poor N2 selectivity was observed over L‐NaBr,L‐KBr and L‐CaBr catalysts.The decrease in the ratio of chemisorbed oxygen to total surface oxygen(Oα/(Oα+Oβ+Ow)),reducibility and surface acidity might contribute to the poor activity and N2 selectivity over L‐KBr catalyst.The increased Oαratio was conducive to the enhanced reducibility of L‐CaBr.Combined with enhanced surface acidity,this might offset the negative effect of the loss of active sites by CaBr2 covering.The overoxidation of NH3 and poor N2 selectivity in NH3 oxidation should retard the SCR activity at high temperatures over L‐CaBr catalyst.The increased basicity might contribute to increased NOx adsorption on L‐KBr and L‐CaBr catalysts.A correlation between the acid‐basic and redox properties of bromide‐poisoned catalysts and their catalytic properties is established.

Membrane-based air dehumidification:A comparative review on membrane contactors,separative membranes and adsorptive membranes

This review compares the different types of membrane processes for air dehumidification.Three main categories of membrane-based dehumidification are identified–membrane contactors using porous membranes with concentrated liquid desiccants,separative membranes using dense membrane morphology with a pressure gradient to drive the separation of moisture from air,and adsorptive membranes using nanofibrous membranes which adsorb and capture moisture to realise dehumidification.Drawing upon the importance of dehumidification and humidity control for urban sustainability and energy efficacy,this review critically analyses and recognizes the three unique categories of membrane-based air dehumidification technologies.Essentially,the discussion is broken into three sections-one for each category-discriminating in terms of the driving force,membrane structure and properties,and its performance indicators.Readers will notice that despite having the same objective to dehumidify air,the polymers used amongst each category differs to suit the operating requirements and optimize dehumidification performance.At the end of each section,a performance table or summary of dehumidifying membranes in its class is provided.The final section concludes with a comparative review of the three categories on membrane-based air dehumidification technologies and draw inspiration from parallel research to rationalise the potential and innovative use of promising materials in membrane fabrication for air dehumidification.

Nitrogen-doped iron for selective catalytic reduction of nitrate to dinitrogen

Nitrate is the leading cause of eutrophication worldwide and is one of the most challenging pollutants for restoration of polluted surface waters such as lakes, rivers and reservoirs. We report herein a new architecture of iron nanoparticles for high-efficiency denitrification by selective reduction of nitrate (NO3-) to dinitrogen (N2). The iron nanoparticles are doped with nitrogen (FeN) and encapsulated within a thin layer of nitride-carbon (NC). The nanoparticles have high pyrrolic N content (17.4 at.%) and large specific surface area (2040 m2/g). Laboratory experiments demonstrated high N2selectivity (91%) and nitrate removal capacity (6004 mg N/g Fe) for treatment of nitrate-containing water. This iron-based nanomaterial overcomes shortcomings of conventional catalysts by eliminating the use of precious and toxic heavy metals (e.g., Pd, Pt, Cu, Ni) and minimizing the generation of undesirable byproducts (e.g., ammonia) from the reactions with nanoscale zero-valent iron (n ZVI). The multiple electron transfers process from NO3- to N2can be fine-tuned by adjusting the NC shell thickness. Superior electrocatalytic perfor- mance, low cost and minimal environmental impact of the iron-derived nanocatalyst offer promising prospects for water purification, waste treatment and environmental remediation.

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.

Study on Oxidation Activity of CuCeZrO_x Doped with K for Diesel Engine Particles in NO/O_2

CuCeZrO_x and KCuCeZrO_x catalysts were synthesized and coated on the blank diesel particulate filter(DPF)substrate and a particulate matter(PM)loading apparatus was used for soot loading.The catalytic performances of soot oxidation were evaluated by temperature programmed combustion(TPC)test and characterization tests were conducted to investigate the physicochemical properties of the catalysts.The reaction mechanism in the oxidation process was analyzed with diffuse reflectance infrared Fourier transform spectroscopy.The results demonstrated that CuCeZrO_x catalyst exhibited high activities of soot oxidation at low temperature and the best results have been attained with Cu_(0.9)Ce_(0.05)Zr_(0.05)O_x over which the maximum soot oxidation rate decreased to 410~?C.Characterization tests have shown that catalysts containing 90%Cu have uniformly distributed grains and small particle sizes,which provide excellent oxidation activity by providing more active sites and forming a good bond between the catalyst and the soot.The low-temperature oxidation activity of soot could be further optimized due to the excellent elevated NO’s conversion rate by partially substituting Cu with K.The maximum particle oxidation rate can be easily realized at such a low temperature as 347~?C.