Ulriksennicolaisen2142

Amorphous titania samples prepared by ammonia solution neutralization of titanyl sulphate have been characterized by chemical and thermal analyses, and with reciprocal-space and real-space fitting of wide-angle synchrotron X-ray scattering data. A model that fits both the chemical and structural data comprises small segments of lepidocrocite-type layer that are offset by corner-sharing as in the monoclinic titanic acids H2Ti n O2n+1·mH2O. The amorphous phase composition that best fits the combined chemical and scattering data is [(NH4)3H21Ti20O52]·14H2O, where the formula within the brackets is the cluster composition and the H2O outside the brackets is physically adsorbed. The NH4 + cations are an integral part of the clusters and are bonded to layer anions at the corners of the offset layers, as occurs in the alkali metal stepped-layer titanates. The stepped-layer model is shown to give a consistent mechanism for the reaction of aqueous ammonia with solid hydrated titanyl sulphate, in which the amorphous product retains the exact size and shape of the reacting titanyl sulphate crystals.High performance supercapacitor without binders has attracted wide attention as an energy storage device. In this work, novel NH4V4O10 nanobelts were successfully synthesized and decorated into TiN nanotube arrays by a simple hydrothermal method. The as-prepared no-binder electrode hybrids exhibited excellent electrochemical performances with a specific capacitance of 749.0 F g-1 at 5 mV s-1 and a capacity retention of 85.7% after 200 cycles, which makes it an appealing candidate for electrode materials of supercapacitors.Based on density functional theory combined with low-energy models, we explore the magnetic properties of a hybrid atomic-thick two-dimensional (2D) material made of germanene doped with fluorine atoms in a half-fluorinated configuration (Ge2F). The Fluorine atoms are highly electronegative, which induces magnetism and breaks inversion symmetry, triggering thereby a finite and strong Dzyaloshinskii-Moriya interaction (DMI). The magnetic exchange interactions are of antiferromagnetic nature among the first, second and third neighbors, which leads to magnetic frustration. The Néel state is found to be the most stable state, with magnetic moments lying in the surface plane. This results from the out-of-plane component of the DMI vector, which seems to induce an effective in-plane magnetic anisotropy. Upon application of a magnetic field, spin-spirals and antiferromagnetic skyrmions can be stabilized. We conjecture that this can be realized via magnetic exchange fields induced by a magnetic substrate. To complete our characterization, we computed the spin-wave excitations and the resulting spectra, which could be probed via electron energy loss spectroscopy, magneto-Raman spectroscopy or scanning tunneling spectroscopy.Organic polymer/inorganic particle composites with thermoelectric (TE) properties have witnessed rapid progress in recent years. Nevertheless, both development of novel polymers and optimization of compositing methods remain highly desirable. In this study, we first demonstrated a simulated in situ coagulation strategy for construction of high-performance thermoelectric materials by utilizing single-walled carbon nanotubes (SWCNTs) and a new D-A polymer TPO-TTP12 that was synthesized via incorporating dioxothiopyrone subunit into a polymeric chain. It was proven that the preparation methods have a significant influence on thermoelectric properties of the TPO-TTP12/SWCNT composites. The in situ prepared composite films tend to achieve much better thermoelectric performances than those prepared by simply mixing the corresponding polymer with SWCNTs. As a result, the in situ compositing obtains the highest Seebeck coefficient of 66.10 ± 0.05 μV K-1 at the TPO-TTP12-to-SWCNT mass ratio of 1/2, and the best electrical conductivity of up to 500.5 ± 53.3 S cm-1 at the polymer/SWCNT mass ratio of 1/20, respectively; moreover, the power factor for the in situ prepared composites reaches a maximum value of 141.94 ± 1.47 μW m-1 K-2, far higher than that of 104.68 ± 0.86 μW m-1 K-2 for the by-mixing produced composites. This indicates that the dioxothiopyrone moiety is a promising building block for constructing thermoelectric polymers, and the simulated in situ compositing strategy is a promising way to improve TE properties of composite materials.In situ generation is a powerful technique used to prepare homogenous adsorptive mixed matrix membranes (MMMs) containing functional nanoparticles, although the mechanism of formation of the membranes is not yet clear and there have been few published evaluations of membrane fouling. We therefore used this method to prepare a novel homogeneous adsorptive Zr-based nanoparticle-polyethersulfone (PES) MMM and systematically studied the mechanism of membrane formation at the atomic level. As the amount of ZrOCl2·8H2O in the casting solution increased, the phase inversion kinetics changed from instantaneous demixing due to the thermodynamic enhancement effect to a delayed demixing process caused by viscosity hindrance. The in situ generation of nanoparticles in these MMMs can be divided into three stages the migration stage, the exfoliation stage and the stable stage. Our findings provide a fundamental understanding of the interface chemistry in the development of in situ generated MMMs. M2 showed a higher adsorption of As(v) than the pure PES membrane and could be reused after regeneration. The removal of As(v) from the M2 filtration system mainly took place via adsorption rather than size exclusion, as confirmed by EDS and experimental data. The presence of humic acid slightly inhibited the removal of As(v) during the filtration process as a result of the barrier effect caused by the formation of a filter cake via humic acid fouling. The filtration of a bovine serum albumin solution showed that the MMM with in situ generated nanoparticles had better antifouling properties than the PES membrane alone in multiple applications as a result of the enhanced hydrophilic surface.A series of micro-mesoporous activated carbons (ACs) were prepared from sugar beet residue by a two-step method including KOH chemical activation and were used for Cr(vi) removal from aqueous solutions. Several characterization techniques, including SEM, TEM, N2 adsorption, XRD, FTIR, and Raman spectroscopy, were used to determine the chemical and physical characteristics of the ACs, and the adsorption properties of the ACs were tested. The results indicated that the high specific surface area of the ACs reached 2002.9 m2 g-1, and the micropore surface area accounts for 85% of the total area. The optimal conditions for achieving the maximum Cr(vi) adsorption capacity of 163.7 mg g-1 by the ACs were activation with a KOH/carbon ratio of 3.0, an initial Cr(vi) concentration of 400 mg L-1, an adsorbent dose of 2.0 g L-1 and pH of 4.5. fMLP Therefore, the ACs exhibit excellent adsorption performance for removing Cr(vi) from aqueous solutions. According to an investigation of the adsorption process, the adsorption isotherm is most consistent with the Langmuir isotherm model, and the adsorption kinetics were well described by the pseudo-second-order model.The study of the recent colonization of a symbiont and its interaction with host communities in new locations is an opportunity to understand how they interact. The use of isotopic ratios in trophic ecology can provide measurements of a species' isotopic niche, as well as knowledge about how the isotopic niches between symbiont and host species overlap. Stable isotope measurements were used to assess the sources of carbon assimilated by the host species (the bivalves Mytilus galloprovincialis and Scrobicularia plana) and their associated symbiont pea crab Afropinnotheres monodi, which occurs within these bivalves' mantle cavities. The mixing model estimates suggest that all of them assimilate carbon from similar sources, particularly from pseudofaeces and particulate organic matter in this symbiotic system based on filter feeding. The symbiotic species occupy comparable trophic levels and its association seems to be commensal or parasitic depending on the duration of such association. The pea crab A. monodi reflects a sex-specific diet, where males are more generalist than the soft females because the latter's habitat is restricted to the host bivalve. The high isotopic overlap between soft females and M. galloprovincialis may reflect a good commensal relationship with the host.Vedolizumab has become an integral part of the therapeutic armamentarium for patients with inflammatory bowel disease (IBD) who have failed conventional medical therapy. Vedolizumab is an α4β7 integrin antagonist that inhibits intestinal T-cell translocation by blocking integrin interactions with mucosal vascular addressin cellular adhesion molecule 1, reducing lymphocyte-mediated inflammation.1 Its gut selective mode of action and favorable safety profile have led to reports of off-label use for non-IBD-related inflammatory intestinal disorders, such as microscopic colitis,2 and small intestinal inflammatory conditions including autoimmune enteropathy3 and common variable immune deficiency-related enteritis.4 Treatment of non-IBD-related enteropathies is challenging with no approved therapies or established treatment algorithms. We conducted a literature review to assess clinical, endoscopic, and histologic improvement in patients treated with vedolizumab for non-IBD enteropathies refractory to conventional therapy.Zirconia supported vacant phosphotungstate stabilized Pd nanoparticles (Pd-PW11/ZrO2) were prepared using a simple impregnation and post reduction method, characterized and their efficiency for selective C[double bond, length as m-dash]C hydrogenation of unsaturated compounds explored. The establishment of a hydrogenation strategy at low temperature using water as solvent under mild conditions makes the present system environmentally benign and green. The catalyst shows outstanding activity (96% conversion) with just a small amount of Pd(0) (0.0034 mol%) with high substrate/catalyst ratio (29 177/1), TON (28 010) and TOF (14 005 h-1) for cyclohexene (as a model substrate) hydrogenation. The catalyst was recovered by simple centrifugation and reused for up to five catalytic cycles without alteration in its activity. The present catalyst was found to be viable towards different substrates with excellent activity and TON (18 000 to 28 800). A study on the effect of addenda atom shows that the efficiency of the catalyst can be enhanced greatly by increasing the number of counter protons. This challenging strategy would greatly benefit sustainable development in chemistry as it diminishes the use of organic solvents and offers economic and environmental benefits as water is cheap and non-toxic.In this work, new double perovskite Tb2ZnMnO6 nanoparticles were successfully synthesized by a sol-gel auto combustion method. To synthesize these nanoparticles, three known sugars, lactose, fructose, and maltose, and liquorice powder, which contains quantities of sugar and other organic compounds, were used as fuel. Images obtained from Scanning Electron Microscopy (SEM) analysis implied that maltose-based nanoparticles are homogenous and less in particle size. Further, different maltose ratios were applied to get the best size and morphology. The optimum sample was used to continue the other analysis to check other features of the nanoparticles. Also, the optimum sample was used for the removal of dye contamination under the photocatalytic process. Photocatalytic tests were performed in neutral and alkaline pH conditions under UV-light irradiation. It has been found that the decolorization percent for methyl orange was about 35% and for methyl violet about 55% at neutral pH. Also, this value for methyl violet was about 90% at pH = 8.