In‐Depth Study of Mass Transfer in Nanoporous Materials by Micro‐Imaging

The first application of interference microscopy to monitoring mass transfer in nanoporous materials dates back to late 1970s when Caro and colleagues reported results of investigations of water uptake by LTA type zeolites. It was, however, not before the beginning of the new millennium that the developments in both the measuring technique and computational power have enabled the recording of transient guest profiles during molecular uptake and release under well‐defined conditions, leading to the establishment of a novel access to diffusion studies, now referred to as micro‐imaging. In the present contribution, the thus accessible novel type of information is illustrated by an in‐depth analysis of the uptake kinetics of methanol in an all‐silica ferrierite. In particular, two remarkable experimental findings are reported, which may be tracked back to their microstructural and/or microdynamic origin, namely a pronounced asymmetry in the transient concentration profiles and a slowing down of guest uptake with increasing temperature.     

Electrostatic assembly of nanoparticles and biomacromolecules

The controlled assembly of nanoparticles in thin film form on solid supports, both as monolayers and as superlattice structures, is a problem of considerable topical interest. Among the many interactions used to program the assembly of nanoparticles, electrostatic forces are particularly interesting for many reasons. This Account deals with assembling surface-modified nanoparticles in thin film form using electrostatic interactions at the air-water interface and in thermally evaporated lipid films. The generality of the electrostatic assembly protocol is demonstrated in the immobilization of DNA and proteins in lipid films.     

Pressure drop for single and two‐phase flow of non‐newtonian liquids in helical coils

New experimental results on pressure loss for the single and two‐phase gas‐liquid flow with non‐Newtonian liquids in helical coils are reported. For a constant value of the curvature ratio, the value of the helix angle of the coils is varied from 2.56° to 9.37°. For single phase flow, the effect of helix angle on pressure loss is found to be negligible in laminar flow regime but pressure loss increases with the increasing value of helix angle in turbulent flow conditions. On the other hand, for the two‐phase flow, the well‐known Lockhart‐Martinelli method correlates the present results for all values of helix angle (2.56‐9.37°) satisfactorily under turbulent/laminar and turbulent/turbulent conditions over the following ranges of variables as: 0.57 ≤ n′ ≤ 1; Re′ < 4000; Re_l < 4000; Re_g < 8000; 8 ≤ x ≤ 1000 and 0.2 ≤ De′ ≤ 1000.     

Fiber-Matrix Interfacial Adhesion Improvement in Carbon Fiber-Bisphenol-A Polycarbonate Composites by Polymer Grafting

Fiber-matrix interfacial adhesion in thermoplastic composites is generally poor due to the lack of formation of strong covalent and/or ionic bonds between the generally inert thermoplastic resins and the surface of the reinforcing fiber. Adhesion can be improved by forming covalent linkages between the fiber and the matrix by grafting a polymer of appropriate compatibility, molecular weight, and sufficient density onto the surface of the fiber. We have grafted low molecular weight polycarbonate and polymethyl methacrylates onto the surface of carbon fibers and measured an improvement in the level of adhesion ranging from 25% to100% over the ungrafted composites. It was also observed that the level of improvement in adhesion appears to be independent of the molecular weight of the grafted polymer. Examination of the fracture surface of these composites reveals that the failure is cohesive in the matrix for the polymer grafted fiber composites, while it is adhesive for the ungrafted composites.     

Low-Temperature Synthesis of Calcium Hexa-Aluminate

Calcium hexa-aluminate (CaO·6Al₂O₃) has been prepared from calcium nitrate and aluminum sulfate solutions in the temperature range of 1000°–1400°C. A 0.3 mol/L solution of aluminum sulfate was prepared, and calcium nitrate was dissolved in it in a ratio that produced 6 mol of Al₂(SO₄)₃·16H₂O for each mole of Ca(NO₃)₂·4H₂O. It was dried over a hot magnetic stirrer at ∼70°C and fired at 1000°–1400°C for 30–360 min. The phases formed were determined by XRD. It was observed that CaO·Al₂O₃ and CaO·2Al₂O₃ were also formed as reaction intermediates in the reaction mix of CaO·6Al₂O₃. The kinetics of the formation of CaO·6Al₂O₃ have been studied using the phase-boundary-controlled equation 1 − (1 − x )^1/3= K log t and the Arrhenius plot. The activation energy for the low-temperature synthesis of CaO·6Al₂O₃ was 40 kJ/mol.     

Dietary Intake and Food Sources of Total and Individual Polyunsaturated Fatty Acids in the Belgian Population Over 15 Years Old

Advances in our knowledge of the physiological functions of dietary polyunsaturated fatty acids (PUFAs) have led to an increased interest in food sources and the level of dietary intake of these nutrients. Up to now, no representative data was available for the Belgian adult population. This study aimed to describe data on the intake and food sources of total and individual omega-6 and omega-3 PUFA for the Belgian population over 15 years old. PUFA intakes were assessed for 3,043 Belgian adults, based on two non-consecutive 24 h recalls. Usual intakes were calculated using the multiple source method. The results showed that the intake of linoleic acid (LA) is in accordance with the recommendation for almost all Belgian adults. However, the intake of omega-3 PUFA is suboptimal for a large part of the studied population and also the intake of total PUFA should be increased for a part of the population. The main food source of LA and α-linolenic acid (ALA) was the group of fats and oils (60.6 % for LA and 53.1 % for ALA). Fish and fish products were the most important sources of long chain omega-3 PUFA. Age influenced fatty acids intake, with higher intake of omega-3 PUFA in the older age groups. To fill the gap between the intake and recommendation of total PUFA, and in particular omega-3 PUFA, sustainable strategies and efficient consumer communication strategies will be needed.     

Synthesis and characterization of polymeric plasticizer from PET waste and its applications in nitrile rubber and nitrile–PVC blend

Polyethylene terephthalate (PET) waste is not biodegradable; thus, it will create environmental hazards if disposed in landfills. Therefore, the only way of addressing the problem of disposal of post-industrial and post-consumer PET wastes is through recycling. The polyester plasticizer for polyacrylonitrile butadiene rubber (NBR) and polyacrylonitrile butadiene–polyvinylchloride rubber blend (NBR–PVC) was obtained by the depolymerization of PET waste with 2-ethyl-1-hexanol. The PET waste was depolymerized until a polymeric plasticizer with the average molecular weight in the range of 450–900 g/mol was obtained. The polymeric plasticizer was characterized for acid and hydroxyl numbers, viscosity, density, FTIR, NMR and TGA/DTA thermogram. The prepared polymeric plasticizer was used in the preparation of nitrile rubber and nitrile–PVC rubber blend rubber sheets, where these sheets were tested for compatibility, tensile strength, elongation-at-break, hardness and ageing properties. Nitrile rubber and nitrile–PVC blend sheets were also prepared using DOP as a plasticizer and a comparative study with the synthesized polymeric plasticizer was made. It was observed that synthesized polymeric plasticizer provides excellent tensile properties and ageing resistance for high-performance applications as compared to that obtained from DOP. The end uses for nitrile rubber and nitrile–PVC rubber blend compounds are quite diverse, but they can be loosely categorized as being either general performances or higher performance applications. Each of these performance categories requires a different set of considerations in terms of compounding with plasticizers.     

Investigation of the Effect of Accelerated Hydrothermal Aging on the Cu Sites in a Cu-BEA Catalyst for NH3-SCR Applications

The influence of hydrothermal aging between 500 and 900 °C for 3 h, on the structure of a Cu-Beta catalyst was studied in this work. The XRD measurements indicated a structural breakdown of the zeolite upon 900 °C hydrothermal aging. This was confirmed from the loss of surface area as measured by BET method. The temperature for the zeolite structure break down was different between the powder bed as opposed to the sample that was washcoated on a cordierite monolith, which was most likely due to slightly different aging conditions and the presence of binders. The strong increase in the intensity of the Cu2p XPS peak indicated that the surface is enriched of copper at higher temperatures due to the zeolite structure collapse. The presence of CuO is usually accompanied by a satellite peak, which was clearly observed at higher binding energies for the catalysts aged at 800 and 900 °C. The XPS results are in good agreement with the UV–Vis experiments, which also point to the formation of copper oxide after high temperature aging.     

Evaluation of the economic and environmental impact of combining dry reforming with steam reforming of methane

Lately, there has been considerable interest in the development of more efficient processes to generate syngas, an intermediate in the production of fuels and chemicals, including methanol, dimethyl ether, ethylene, propylene and Fischer–Tropsch fuels. Steam methane reforming (SMR) is the most widely applied method of producing syngas from natural gas. Dry reforming of methane (DRM) is a process that uses waste carbon dioxide to produce syngas from natural gas. Dry reforming alone has not yet been implemented commercially; however, a combination of steam methane reforming and dry reforming of methane (SMR + DRM) has been used in industry for several years.     

Solution Structure and Dynamics of the Small Protein HVO_2922 from Haloferax volcanii

Past sequencing campaigns overlooked small proteins as they seemed to be irrelevant due to their small size. However, their occurrence is widespread, and there is growing evidence that these small proteins are in fact functionally very important in organisms found in all kingdoms of life. Within a global proteome analysis for small proteins of the archaeal model organism Haloferax volcanii, the HVO_2922 protein has been identified. It is differentially expressed in response to changes in iron and salt concentrations, thus suggesting that its expression is stress-regulated. The protein is conserved among Haloarchaea and contains an uncharacterized domain of unknown function (DUF1508, UPF0339 family protein). We elucidated the NMR solution structure, which shows that the isolated protein forms a symmetrical dimer. The dimerization is found to be concentration-dependent and essential for protein stability and most likely for its functionality, as mutagenesis at the dimer interface leads to a decrease in stability and protein aggregation.