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Experimental results indicated that that P3 can act as bifunctional hybrid material to solve environmental issues.

Experimental results indicated that that P3 can act as bifunctional hybrid material to solve environmental issues.Colloidal interactions between clay nanoparticles have been studied extensively because of their strong influence on the hydrology and mechanics of many soils and sedimentary media. The predominant theory used to describe these interactions is the Derjaguin-Landau-Verwey-Overbeek (DLVO) model, a framework widely applied in colloidal and interfacial science that accurately predicts the interactions between charged surfaces across water films at distances greater than ~ 3 nm (i.e., ten water monolayers). Unfortunately, the DLVO model is inaccurate at the shorter interparticle distances that predominate in most subsurface environments. For example, it inherently cannot predict the existence of equilibrium states wherein clay particles adopt interparticle distances equal to the thickness of one, two, or three water monolayers. Molecular dynamics (MD) simulations have the potential to provide detailed information on the free energy of interaction between clay nanoparticles; however, they have only been used to examine clay swelling and aggregation at interparticle distances below 1 nm. We present the first MD simulation predictions of the free energy of interaction of smectite clay nanoparticles in the entire range of interparticle distances from the large interparticle distances where the DLVO model is accurate (>3 nm) to the short-range swelling states where non-DLVO interactions predominate ( less then 1 nm). Our simulations examine a range of salinities (0.0 to 1.0 M NaCl) and counterion types (Na, K, Ca) and establish a detailed picture of the breakdown of the DLVO model. In particular, they confirm previous theoretical suggestions of the existence of a strong non-DLVO attraction with a range of ~ 3 nm arising from specific ion-clay Coulomb interactions in the electrical double layer.Selective dehydrogenation of formic acid is regarded as a universal strategy for providing a clean energy carrier (hydrogen, H2) to reduce the dependence on fossil fuel. In this work, ultrafine PdAg nanoparticles (NPs) are successfully immobilized on NH2-functionalized metal-organic framework MIL-101(Cr) by a facile wet-reduction method. By virtue of amine group, the size of obtained PdAg NPs can be controlled into 2.2 nm, which are monodispersed on NH2-MIL-101(Cr) surface. In addition, the resulting Pd0.8Ag0.2 NPs/NH2-MIL-101(Cr) catalyst systems demonstrate excellent catalytic activity for formic acid decomposition in mild condition, the turn over frequency (TOF) value can achieve as high as 1475 h-1 at 323 K, which is comparable to most of the reported noble metal heterogeneous catalysts for this catalytic reaction under similar conditions. The excellent catalytic kinetics is mainly attributed to the ultrafine size and high dispersion of PdAg NPs. Also, the amine group from NH2-MIL-101(Cr) support facilitates the OH bond dissociation of formic acid and improves the kinetics of formic acid decomposition.Paracetamol is the most commonly used antipyretic and analgesic drug in the world. read more The key challenge in paracetamol therapy is associated with the frequency of the dosing. Depending on the gastric filling within 10-20 min paracetamol is released and rapidly absorbed from the gastrointestinal tract. Therefore, it must be taken three or four times a day. To address the dose challenge it is desirable that the paracetamol release profile follows the zero-order kinetic model (constant rate of drug release per unit time). This goal can be achieved by using a suitable porous carrier system. Herein, non-toxic wrinkled mesoporous carbons with unique morphology were synthesized via the hard template method as new carriers for paracetamol. These particles can precisely modulate the release of paracetamol over 24 h in a simulated gastric fluid according to the zero-order kinetic model completely eliminating the initial burst release. Overall, these systems could significantly enhance the bioavailability of paracetamol and prolong its therapeutic effect in numerous diseases such as cold, flu, COVID-19, and severe pain.As an important biomarker, the analysis of cytochrome c (Cyt c) plays a crucial role in cell-apoptosis or even cancer diagnosis. This work develops a label-free probe for Cyt c using the nitrogen and fluorine co-doped carbon dots (N, F-CDs) which were facile prepared through solvothermal method with 3, 4-difluorophenylhydrazine as precursor. The N, F-CDs have an average diameter of 3.4 nm, and can form a quite stable colloidal solution. The N, F-CDs show bright yellow-green fluorescence, excitation/emission wavelengths 475/530 nm, and a relatively high fluorescence quantum yield of 16.9%. Interestingly, the N, F-CDs indicate a linear and reversible variation of emission intensity with a sensitivity of -1.11% per ℃ in the temperature range from 25 to 60 ℃. Inner filter effect (IFE) between N, F-CDs and Cyt c turns the fluorescence of N, F-CDs from "on" to "off". The sensor possesses the excellent anti-interference ability towards the main components of plasma. Under optimum conditions, there is a linear relationship between fluorescence intensity function (F0-F) and the concentration of Cyt c in the range of 0.5-25 μΜ with a limit of detection (LOD) (S/N = 3) of 0.25 μM. Finally, the developed method has been successfully used to detect Cyt c in human serum sample with satisfactory recoveries in a range of 93.14-110.40%.Climate change, global warming, and population growth have led researchers to use eco-sociable procedures for the N2 reduction reaction. It has discovered that N2 molecule can be transformed into NH3 in ambient circumstances with nanocomposites upon visible irradiation. In this research paper, a new visible-light-driven photocatalyst was constructed, with various weight percents of FeOCl particles (10, 20, 30, and 40%) that have adhered on NS-CN. Subsequently, multiple features of the nanocomposites were assayed in detail. The results illustrated that the NS-CN/FeOCl (20%) system has remarkable photoactivity in the NH4+ production reaction in comparison with the NS-CN and CN, which showed 2.5 and 8.6 higher activity, respectively. The durability of NS-CN/FeOCl (20%) system, as a substantial factor, was assayed for 5 recycles. Moreover, the effect of electron quenchers, pH of media, and solvent was studied. At last, a feasible Z-scheme mechanism for the remarkable improvement of N2 fixation efficiency was offered.

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