Candida antarctica Lipase B Immobilized onto Chitin Conjugated with POSS? Compounds: Useful Tool for Rapeseed Oil Conversion

A new method is proposed for the production of a novel chitin-polyhedral oligomeric silsesquioxanes (POSS) enzyme support. Analysis by such techniques as X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy confirmed the effective functionalization of the chitin surface. The resulting hybrid carriers were used in the process of immobilization of the lipase type b from Candida antarctica (CALB). Fourier transform infrared spectroscopy (FTIR) confirmed the effective immobilization of the enzyme. The tests of the catalytic activity showed that the resulting support-biocatalyst systems remain hydrolytically active (retention of the hydrolytic activity up to 87% for the chitin + Methacryl POSS^® cage mixture (MPOSS) + CALB after 24 h of the immobilization), as well as represents good thermal and operational stability, and retain over 80% of its activity in a wide range of temperatures (30–60 °C) and pH (6–9). Chitin-POSS-lipase systems were used in the transesterification processes of rapeseed oil at various reaction conditions. Produced systems allowed the total conversion of the oil to fatty acid methyl esters (FAME) and glycerol after 24 h of the process at pH 10 and a temperature 40 °C, while the Methacryl POSS^® cage mixture (MPOSS) was used as a chitin-modifying agent.     

Lining-Up Control Strategies for N-trailer Vehicles

Maneuvers performed with tractor-trailers vehicles (N-trailers) belong to the most demanding motion control tasks in the transportation practice. Very frequent maneuvers concern the lining-up process of a vehicle chain, usually as a preliminary stage which prepares the system to subsequent parking/docking maneuvers. The most common lining-up control approach results from utilization of the open-loop asymptotic stability of N-trailer joint-angle dynamics in the forward motion. However, in case of long trailers this approach appears very inefficient especially if the available motion space is substantially limited. By using the triangular forms of joint-angle dynamics the problem of lining-up control for N-trailers is analyzed in the paper by considering two alternative strategies: active lining-up (feedback control) and passive lining-up (open-loop control). The two strategies are compared in the context of their practical effectiveness, and how the effectiveness depends on kinematic parameters of the trailers and their interconnections. It is revealed why the active strategy can be much more efficient in most practical cases. Theoretical considerations are validated by results of numerical simulations and experiments conducted with a laboratory-scale three-trailer robotic vehicle.     

Modeling of thermally induced damage in the processing of Cr–Al2O3 composites

Thermal stresses induced during the cooling of Cr–Al₂O₃ (MMC) processed by sintering are modeled numerically using the FEA. The composite microstructure is modeled as (i) random distribution of ceramic particles (voxels) in the metal matrix, and (ii) using micro-CT scans of the real microstructure transformed into a FE mesh. Numerical simulations of the thermal residual stresses are compared with the test data measured by X-ray diffraction. A simple numerical model is then proposed to predict the overall elastic properties of the composite with account of the porosity and damage induced by the thermal stresses. Comparison of the model predictions with the measured data for Young’s modulus is presented.     

Can ‘negative net CO2 emissions’ from decarbonised biogas-to-electricity contribute to solving Poland’s carbon capture and sequestration dilemmas?

The article analyses to what extent ‘negative net CO₂ emissions’ from decarbonised biogas-to-electricity can contribute to solving Poland’s carbon capture and sequestration dilemmas. From the criteria-based evaluation of low-carbon power technologies it is found, that biogas-to-electricity is among technologies having increasing production potential in Poland. Therefore, in future biogas will be able to contribute to solving Poland’s CCS dilemmas, because it offers carbon-neutral electricity. Moreover, by applying CCS into biogas-to-electricity the ‘negative net CO₂ emissions’ can be achieved. The article examines three biogas-to-electricity technologies involving CO₂ capture, i.e. biogas-to-biomethane, biogas-to-CHP and biogas-to-electricity via the ORFC cycle. It is emphasised that the ORFC cycle offers low-cost CO₂ separation from a CO₂-H₂ mixture, low O₂-intensity, and the opportunities for advanced mass and energy integration of involved processes. Besides, energy conversion calculations show that the ORFC cycle can offer comparable cycle efficiency with air- and oxy-combustion combined cycles. In regard to the design of biogas-based energy systems it is recommended to include (i) distributed production of biogas in order to avoid costs of long-distance transportation of high-moisture content biomass and (ii) centralised large-scale decarbonised biogas-to-electricity power plants since costs of pipeline transportation of gases are low but large-scale plants could benefit from increased energy and CCS efficiencies.     

A Solid-State NMR Study of Selenium Substitution into Nanocrystalline Hydroxyapatite

The substitution of selenium oxyanions in the hydroxyapatite structure was examined using multinuclear solid-state resonance spectroscopy (ssNMR). The study was supported by powder X-ray diffractometry (PXRD) and wavelength dispersion X-ray fluorescence (WD-XRF). Samples of pure hydroxyapatite (HA₃₀₀) and selenate (HA₃₀₀-1.2SeO₄) or selenite (HA₃₀₀-1.2SeO₃) substituted hydroxyapatites were synthesized using the standard wet method and heated at 300 °C to remove loosely bonded water. PXRD data showed that all samples are single-phase, nanocrystalline hydroxyapatite. The incorporation of selenite and selenate ions affected the lattice constants. In selenium-containing samples the concentration of Se was very similar and amounted to 9.55% and 9.64%, for HA₃₀₀-1.2SeO₄ and HA₃₀₀-1.2SeO₃, respectively. PXRD and ssNMR data showed that the selenite doping significantly decreases the crystallite size and crystallinity degree. ³¹P and ¹H NMR experiments demonstrated the developed surface hydrated layer in all samples, especially in HA₃₀₀-1.2SeO₃. ¹H NMR studies showed the dehydroxylation of HA during the selenium oxyanions substitution and the existence of hydrogen bonding in structural hydroxyl group channels. ¹H→⁷⁷Se cross polarization NMR experiments indicated that selenites and selenates are located in the crystal lattice and on the crystal surface.