Comparing global land-cover products – implications for geoscience applications: an investigation for the trans-boundary Mekong Basin

In this article we present the results of a comparison of six globally available land-cover products for the Mekong Basin – an area that spans 795,000 km² and comprises parts of six riparian countries: China, Myanmar, Thailand, Laos, Cambodia, and Vietnam. The basin covers most climatic zones: from high-altitude, snow-covered mountainous regions in the north, to subtropical and tropical rainforest areas and agricultural land further south. The geopolitically important region not only is home to over 72,000,000 inhabitants, but also is a centre of attention of several environmental modelling experts, trying to assess future hydrologic dynamics, climate variability, as well probable land-use developments in the area.

We compare land-cover products of the University of Maryland, UMD 1992–1993, the GLC 2000 product, the GlobCover products of 2004–2006 and 2009, as well as the MODIS-derived land-cover products of 2001 and 2009. For harmonization of individual legends, the Land Cover Classification System, LCCS, has been employed. However, even after harmonization, cross-tabulation among the products reveals extreme differences, where the impact of differing classification algorithms weighs higher than the impact of temporal coincidence of products. Especially, differences within mixed-vegetation classes are large, strongly impacting the overall assessment of forested land, other vegetated land, and even cultivated land in the Mekong Basin. The findings presented here are of high relevance for the modelling community as well as Mekong-related environmental studies, which should consider global remote-sensing-derived products with caution and solid background knowledge.     

IISPH‐FLIP for incompressible fluids

We propose to use Implicit Incompressible Smoothed Particle Hydrodynamics (IISPH) for pressure projection and boundary handling in Fluid‐Implicit‐Particle (FLIP) solvers for the simulation of incompressible fluids. This novel combination addresses two issues of existing SPH and FLIP solvers, namely mass preservation in FLIP and efficiency and memory consumption in SPH. First, the SPH component enables the simulation of incompressible fluids with perfect mass preservation. Second, the FLIP component efficiently enriches the SPH component with detail that is comparable to a standard SPH simulation with the same number of particles, while improving the performance by a factor of 7 and significantly reducing the memory consumption. We demonstrate that the proposed IISPH‐FLIP solver can simulate incompressible fluids with a quantifiable, imperceptible density deviation below 0.1%. We show large‐scale scenarios with up to 160 million particles that have been processed on a single desktop PC using only 15GB of memory. One‐ and two‐way coupled solids are illustrated.     

A microfluidic device for thermal particle detection

We demonstrate the use of heat to count microscopic particles. A thermal particle detector (TPD) was fabricated by combining a 500-nm-thick silicon nitride membrane containing a thin-film resistive temperature detector with a silicone elastomer microchannel. Particles with diameters of 90 and 200 μm created relative temperature changes of 0.11 and ?0.44 K, respectively, as they flowed by the sensor. A first-order lumped thermal model was developed to predict the temperature changes. Multiple particles were counted in series to demonstrate the utility of the TPD as a particle counter.     

Fluidized Bed Air Drying: Experimental Study and Model Development

The presented study describes the processes and mechanisms of batch fluidized bed drying. The influencing factors of hot air drying are theoretically and experimentally examined, in order to present the relations between temperature and humidity profiles and all other drying parameters. A physical model is presented to facilitate the calculation of the drying processes under defined conditions. Three succeeding drying stages are therefore modeled. Mass and energy balances including all components taking part in the process are formulated. The model clarities the drying process under the assumption of pure heat transfer mechanisms. It does not contain adaptive parameters and takes into account an inactive bypass fraction of the fluidization and drying medium. The evaluation of the model was successful for two fluidized bed plants with nominal widths of 100 mm and 400 mm. The experiments showed sufficient accuracy and transferability of the model to equipment of application‐oriented dimensions.     

Enzymatic esterification of glycerol II. Lipase-catalyzed synthesis of regioisomerically pure 1(3)-rac-monoacylglycerols

Regioisomerically pure 1(3)-rac-monoacylglycerols are conveniently prepared in high yields (>75%) and in multigram quantities by enzymatic esterification of glycerol in the presence of various lipases(Chromobacterium viscosum, Rhizopus delemar, Rhizomucor miehei) with a variety of different acyl donors, such as free fatty acids, fatty acid alkyl esters, vinyl esters and triacylglycerols, as well as natural fats and oils. All reactions are carried out in aprotic organic solvents with low water content, namelyn-hexane, diethyl ether, tBuOMe or mixtures of these solvents. Essential for the success of these transformations were the following two factors. First, the creation of an artificial interphase between the solvent-immiscible hydrophilic glycerol and the hydrophobic reaction medium by its adsorption onto a solid support. Second, a facile system for the separation of the desired monoacylglycerol from the reaction mixture, coupled with the continuous recycling of acyl donor and undesirable by-products.     

An in situ Raman study of the intercalation of supercapacitor-type electrolyte into microcrystalline graphite

An initial Raman study on the effects of intercalation for aprotic electrolyte-based electrochemical double-layer capacitors (EDLCs) is reported. In situ Raman microscopy is employed in the study of the electrochemical intercalation of tetraethylammonium (Et₄N⁺) and tetrafluoroborate (BF₄⁻) into and out of microcrystalline graphite. During cyclic voltammetry experiments, the insertion of Et₄N⁺ into graphite for the negative electrode occurs at an onset potential of +1.0 V versus Li/Li⁺. For the positive electrode, BF₄⁻ was shown to intercalate above +4.3 V versus Li/Li⁺. The characteristic G-band doublet peak (E_2g2(i) (1578 cm⁻¹) and E_2g2(b) (1600 cm⁻¹)) showed that various staged compounds were formed in both cases and the return of the single G-band (1578 cm⁻¹) demonstrates that intercalation was fully reversible. The disappearance of the D-band (1329 cm⁻¹) in intercalated graphite is also noted and when the intercalant is removed a more intense D-band reappears, indicating possible lattice damage. For cation intercalation, such irreversible changes of the graphite structure are confirmed by scanning electron microscopy (SEM).     

Enzymatic esterification of glycerol I. Lipase-catalyzed synthesis of regioisomerically pure 1,3-sn-diacylglycerols

Regioisomerically pure 1,3-sn-diacylglycerols are conveniently prepared in high yields (>80%) and in large quantities by enzymatic esterification of glycerol in the presence of various 1,3-selective lipases(Chromobacterium viscosum, Rhizopus delemar, Rhizomucor miehei) and a variety of different acyl donors like free fatty acids, fatty acid alkyl esters and vinyl esters. All reactions are carried out in aprotic organic solvents of low water content, namelyn-hexane, diethyl ether or tBuOMe. The creation of an artificial interphase between the solvent-immiscible hydrophilic glycerol and the hydrophobic reaction media by the adsorption of glycerol onto a solid support prior to use was essential for the success of these transformations. The effects of reaction conditions and the regioselectivities of the lipases on the product yields are described in detail.     

Use of oxygen isotope exchange in CO2 to characterize active sites

The characterization of carbon surface activity in the absence of gasification was attempted using oxygen isotope exchange in CO₂ over spectroscopically pure natural graphite, the surface activity being characterized by the rate of approach to isotopic equilibrium. The probable mechanism of exchange is via the first step in the carbon-CO₂ reaction, the dissociation of CO₂ over a carbon free site: $\text{CO}{}_2\text{+}\text{C}{}_{\mathrm{f}}\text{?}\text{i}{}_1\text{j}{}_1\text{C(O)}\text{+}\text{CO}$. Assuming this mechanism to hold for isotopic exchange, the theoretical rate equation was derived. The rate constants i₁, and j₁, were obtained from previous studies. Theoretical calculations show that the exchange rate is negligible over natural graphite at temperatures much below gasification conditions. Experimental verification of the theoretical analysis was not possible due to the activity of the quartz boat, holding the graphite, for catalyzing the exchange reaction. The exchange reaction was successfully followed over the Pt and CaO supported on a graphitized carbon black, in which case the activity was much, much greater than that ovgr the empty quartz boat.