Catalytic reduction of NOx with H2/CO/CH4 over PdMOR catalysts

Conversion of NO_x with reducing agents H₂, CO and CH₄, with and without O₂, H₂O, and CO₂ were studied with catalysts based on MOR zeolite loaded with palladium and cerium. The catalysts reached high NO_x to N₂ conversion with H₂ and CO (>90% conversion and N₂ selectivity) range under lean conditions. The formation of N₂O is absent in the presence of both H₂ and CO together with oxygen in the feed, which will be the case in lean engine exhaust. PdMOR shows synergic co-operation between H₂ and CO at 450–500 K. The positive effect of cerium is significant in the case of H₂ and CH₄ reducing agent but is less obvious with H₂/CO mixture and under lean conditions. Cerium lowers the reducibility of Pd species in the zeolite micropores. The catalysts showed excellent stability at temperatures up to 673 K in a feed with 2500 ppm CH₄, 500 ppm NO, 5% O₂, 10% H₂O (0–1% H₂), N₂ balance but deactivation is noticed at higher temperatures. Combining results of the present study with those of previous studies it shows that the PdMOR-based catalysts are good catalysts for NO_x reduction with H₂, CO, hydrocarbons, alcohols and aldehydes under lean conditions at temperatures up to 673 K.     

Possibilities of ovum pickup in cattle

Cattle breeding has a new reproduction technique in addition to artificial insemination and embryo transfer. It is the collection of ova from living animal by means of ultrasound guided follicle aspiration (ovum pick-up), followed by embryo-production in vitro. Follicles larger than 2 mm were punctured and the ova were collected twice weekly during 3 months. In total 1677 ova were collected from ten cows; 1342 (80%) were used for in vitro maturation, fertilization, and embryoculture. All ova were fertilized with semen from one bull, and 218 transferable embryos were produced. Calculated on a year basis, this would amount to 87 embryos per animal, with an intra-animal variation between 28 and 132. This new technique may replace MOET (Multiple Ovulation and Embryo Transfer; yearly average of 25 transferable embryos per animal), if the embryo-production via OPU can be performed with semen from any selected bull.     

Localization of acid and alkaline phosphatase

Ultrathin frozen sections of glutaraldehyde fixed yeast cells have been successfully used for the demonstration of acid and alkaline phosphatase. Acid phosphatase was localized over the cell wall of both the mother cell and the bud as well as over the newly forming cross wall (septum). Cytoplasmic vesicles (vacuoles, lysosomes?) located close to the cell wall showed a positive reaction for acid phosphatase as well. After 3 h glutaraldehyde fixation an activation of the nuclear acid phosphatase was observed. Lead precipitates were predominantly found over the nucleolar material of ‘resting’ and budding cells. Alkaline phosphatase could be demonstrated in the ‘yeast-mesosome’ and within the plasmalemma invaginations. After separation of the bud, small vesicles, probably derived from the endoplasmic reticulum showed a strong positive reaction for alkaline phosphatase. In frozen sections incubated for alkaline phosphatase, non-specific lead precipitates were found in the nucleus and along the plasmalemma invaginations.     

Reactive Water Sorbents for the Sorption-Enhanced Reverse Water–Gas Shift

Catalysis Letters - Sorption-enhanced reverse water–gas shift (SE-RWGS, here designated as ‘COMAX’) was studied with bifunctional reactive sorbents. First proof-of-concept is...     

Estimating the gas permeability of commercial volatile corrosion inhibitors at elevated temperatures with thermo-gravimetry

Volatile corrosion inhibitors (VCIs) are incorporated into packaging paper or film to protect metals against atmospheric corrosion. The vapour pressure determines the equilibrium concentration of a volatile corrosion inhibitor (VCI) in the surrounding atmosphere. However, the rate at which the VCI can be delivered across the air gap to a metal surface is determined by the gas permeability. This is the product of the vapour pressure and the diffusion coefficient: S_A = P_AD_AB. The gas permeability of commercial VCIs was estimated at elevated temperatures from vaporisation rates measured using a simple thermo-gravimetric method (TG).     

H/D Exchange on Silica-Grafted Tantalum(V) Imido Amido [(≡SiO)<Subscript>2</Subscript>Ta<Superscript>(V)</Superscript>(NH)(NH<Subscript>2</Subscript>)] Synthesized from Either Ammonia or Dinitrogen: IR and DFT Evidence for Heterolytic Splitting of D<Subscript>2</Subscript>

The silica-grafted Ta^(V) imido amido complex [(≡SiO)₂Ta(NH)(NH₂)], 2, obtained from the reaction of either ammonia or dinitrogen plus hydrogen with the silica-grafted hydrides [(≡SiO)₂Ta^(III)H], 1a, and [(≡SiO)₂Ta^(V)H₃], 1b, undergoes H/D exchange with D₂. In situ IR spectroscopy shows that the fully labelled compound [(≡SiO)₂Ta(ND)(ND₂)], 2-d, can be obtained by moderate heating (60 °C, 3 h) under D₂ atmosphere (550 torr, 300 eq. with respect to Ta), and that the exchange is reversible. The observed stretching and bending frequencies of 2-d are in agreement with the expected isotopic shift upon H/D replacement with respect to literature values reported for 2 and have been corroborated by the independent synthesis of 2-d by reaction of deuterated 1a and 1b with N₂ and D₂. Density functional theory (DFT) calculations, performed using a periodic or a cluster model, explored the structures and energetics of all minima involved in the reaction with H₂ and showed that among the explored pathways the energetically preferred mechanisms for H₂ reaction with [{(μ-O)[(HO)₂SiO]₂}Ta^(V)(NH)(NH₂)], 2q, is the heterolytic cleavage of either the imido Ta=N or the amido Ta-N bonds, to yield respectively [{(μ-O)[(HO)₂SiO]₂}TaH(NH₂)₂], 3q (ΔE = −9.5 kcal mol⁻¹ and ΔG_298K = +2.6 kcal mol⁻¹ with respect to 2q) and [{(μ-O)[(HO)₂SiO]₂}Ta(NH)(NH₃)], 4q (ΔE = −6.0 kcal mol⁻¹ and ΔG_298K = +7.9 kcal mol⁻¹ with respect to 2q). All activation barriers are moderate (between 17.7 and 30.2 kcal mol⁻¹) in agreement with the observed mild heating conditions necessary for the reaction to occur.