Vestroberson5664

Bathochromic or hypsochromic shift-type mechanofluorochromism (b-MFC or h-MFC) was found for (D-π-)2A-type azine-based fluorescent dyes OUY-2, OUK-2, and OUJ-2 possessing intramolecular charge-transfer (ICT) characteristics from two (diphenylamino)carbazole-thiophene units as D (electron-donating group)-π (π-conjugated bridge) moieties to a pyridine, pyrazine, or triazine ring as A (electron-withdrawing group) grinding of the recrystallized dyes induced red or blue shifts of the fluorescent colors, that is, bathochromic or hypsochromic shifts of the fluorescence maximum wavelengths (λfl-solid max). The degrees of MFC evaluated by the absolute value of differences (Δλ fl-solid max) in λfl-solid max before and after grinding of the recrystallized dyes increased in the order of OUY-2 (+7 nm) less then OUK-2 (-17 nm) less then OUJ-2 (+45 nm), so that OUJ-2 exhibits obvious b-MFC, but OUK-2 exhibits h-MFC. X-ray powder diffraction (XRD) and differential scanning calorimetry (DSC) demonstrated that the recrystaystalline state of the recrystallized dyes and the amorphous state of the ground dyes with changes in the intermolecular dipole-dipole and π-π interactions before and after grinding. Moreover, this work reveals that (D-π-)2A fluorescent dyes possessing dipole moments of ca. 3 debye as well as moderate or intense ICT characteristics make it possible to activate the MFC.Dynamicity plays a central role in biological systems such as in the cellular microenvironment. Here, the affinity and dynamics of different guest molecules in a transient supramolecular polymer hydrogel system, i.e. the host network, are investigated. The hydrogel system consists of bifunctional ureido-pyrimidinone (UPy) poly(ethylene glycol) polymers. A monofunctional complementary UPy guest is introduced, designed to interact with the host network based on UPy-UPy interactions. Furthermore, two other guest molecules are synthesized, being cholesterol and dodecyl (c12) guests; both designed to interact with the host network via hydrophobic interactions. At the nanoscale in solution, differences in morphology of the guest molecules were observed. The UPy-guest molecule formed fibers, and the cholesterol and c12 guests formed aggregates. Furthermore, cellular internalization of fluorescent guest molecules was studied. No cellular uptake of the UPy-cy5 guest was observed, whereas the cholesterol-cy5 guest showity for future drug release. However, if modified with cholesterol these guests, or future drugs, will be taken up by cells; if modified with a UPy unit this does not occur. In this way both the drug-hydrogel interaction and the cell internalization behavior can be tuned. Regulating the host-guest dynamics in transient hydrogels opens the door to various drug delivery purposes and tissue engineering.Musk analogues containing different macrocyclic ring systems as well as different annulated ring systems were synthesised by a simple and useful strategy. This strategy includes Eschenmoser-Tanabe fragmentation, enyne metathesis and Diels-Alder reaction as key steps. Starting from easily available (n) macrocyclic ketones, (n + 3) macrocyclic systems were assembled using the basic organic reactions.The simultaneous presence of hazardous chemicals and pathogenic microorganisms in wastewater is tremendously endangering the environment and human health. Therefore, developing a mitigation strategy for adequately degrading toxic compounds and inactivating/killing microorganisms is urgently needed to protect ecosystems. In this paper, the synergetic effects of the photocatalytic activity of TiO2 and Cu-TiO2 nanoparticles (NPs) and the oxidation processes of non-thermal atmospheric pressure plasma (NTAPP) were comprehensively investigated for both the inactivation/killing of common water contaminating bacteria (Escherichia coli (E. coli)) and the degradation of direct textile wastewater (DTW). The photocatalytic NPs were synthesized using the hydrothermal method and further characterized employing field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), ultraviolet-visible diffuse reflection spectroscopy (UV-Vis DRS) and photoluminescence (PL). Results revealed the predominant presence of after plating the treated suspensions on agar, and the degradation of organic compounds in DTW was further validated by measuring the total organic carbon (TOC) removal efficiency. All results collectively revealed that the combinatorial plasma-photocatalysis strategy involving Cu-TiO2 NPs and argon plasma jet produced higher concentrations of ROS and proved to be a promising one-step wastewater treatment effectively killing microorganisms and degrading toxic organic compounds.With the increased demand for high-rate performance Li-ion batteries, it is necessary to find available methods to improve the rate properties of SnO2 electrodes. It is noteworthy that doping was considered to be a feasible means. The electronic structures and diffusion energy barriers of Ni-doped and Ni-N co-doped SnO2 were calculated based on density functional theory. The results estimated that the energy gaps of Ni-doped and Ni-N co-doped SnO2 are 1.07 eV and 0.94 eV, which both are smaller than the value of 2.08 eV of SnO2. These exhibit that the conduction properties of SnO2 can be enhanced by doping with the Ni or Ni-N atoms. Moreover, the diffusion properties of Li can also be improved by doping with Ni-N atoms due to the diffusion energy barrier of Li from the B to C point for Ni-N co-doped SnO2 being 0.12 eV smaller than the value of 0.24 eV for the pristine SnO2. Meanwhile, the diffusion energy barriers of Li along other pathways for Ni-N co-doped SnO2 are almost the same as 0.24 eV for SnO2. These results show that both the electronic and ionic conductivity of SnO2 can be enhanced by Ni-N co-doping, which provides a theoretical explanation to promote the rate properties of SnO2 by Ni-N co-doping as anode materials for Li-ion batteries.Highly crystalline glass-ceramics were successfully manufactured via a one-step direct cooling method using Shuangqishan (Fujian, China) gold tailings as raw materials. A series of glass-ceramics were prepared by controlling the gold tailings addition and post-treatment. X-ray diffraction results show that the crystalline phase of glass-ceramics samples with high tailing addition content (65-80 wt%) is akermanite phase (Ca2MgSi2O7). By contrast, the main phase of 60 wt% and 55 wt% tailings addition samples is diopside (CaMgSi2O6) crystalline phase. In addition, although glass-ceramics have typical fracture characteristics of brittle materials, the crack propagation in the fracture process is disturbed by grains, resulting in the deviation of the fracture path in terms of macroscopic and microcosmic observation. Based on the investigation of samples with different tailings additions, glass-ceramics with 60 wt% tailings contents show excellent mechanical properties with a density of 2.89 g cm-3, a Vickers hardness value of 8.17 GPa, and a flexural strength of 116 MPa after 950 °C heat treatment. Bcl-xL apoptosis This study further confirms the possibility of using Shuangqi Mountain gold tailings as the raw materials for highly crystalline glass-ceramics, which shows great potential for application in mass production.The shuttle effect caused by the soluble long-chain lithium polysulfides greatly hinders the practical application of lithium-sulfur (Li-S) batteries. Therefore, the introduction of suitable anchoring materials is more effective to mitigate this problem. Transition metal phthalocyanines (TMPc) are regarded as a new class of sulfur host materials. Here, 4d transition metal (Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd) decorated phthalocyanines are designed and systematically researched for the performance analysis of anchoring S8/LiPSs by first-principles calculations. The results reveal that the bonding strength of LiPSs can be well adjusted by introducing suitable 4d transition metals into the phthalocyanine structure. The electronic structure analysis indicates the formation of TM-S bonds between the TMPc substrate materials and the LiPSs, which is essential to weaken the Li-S bonds and hence slow down the shuttle effect of LiPSs. ZrPc and NbPc both exhibit excellent potential and thermal stability for facilitating the conversion of LiPSs, as well as a better promoting effect for the sulfur reduction reactions (SRR) with a reduced Gibbs free energy in the rate-determining step (*Li2S2 → *Li2S) during the discharge reaction process. These findings in our work may encourage further experimental and theoretical research for anchoring LiPSs with TMPc as a host material.The self-healing and smart anti-corrosion behavior of a polyurethane coating enhanced with micro-sized capsules have been investigated. An in situ polymerization technique was employed to synthesize a novel microcapsule containing sodium dodecyl sulfate (SDS) as a corrosion inhibitor in linseed oil (LO). FE-SEM, FT-IR and TG analysis were used to characterize the prepared microcapsules. The capsules were separately embedded in polyurethane at 1, 4 and 7 wt% and the coating properties were investigated through the water absorption rate and pull-off adhesion strength. The scratched coating was then subjected to 3.5 wt% NaCl solution to investigate the self-healing ability. Electrochemical measurements were carried out by means OCP, EIS and potentiodynamic polarization and the inhibition mechanism of SDS was discussed in terms of interfacial interactions. Despite the adhesion strength, a positive effect was observed for the water uptake, after addition of the microcapsules. 4 wt% of LO/SDS microcapsules showed the best results as its inhibition efficiency was more than 90% compared to single linseed oil capsules. EDS mapping was also employed to verify the successful release and distribution of the SDS, when subjected to scratching.Electric vehicles (EVs) have been developed to alleviate environmental pollution and climate change, but they leave behind a large amount of retired lithium-ion batteries (LIBs). Since the replacement of LIBs from EVs will lead to considerable waste generation, improving the echelon utilization of retired LIBs is becoming increasingly critical. In this paper, we studied the thermo-electric-electrochemical performance of retired LiFePO4 (LFP) batteries using traditional methods, and found that the remaining capacity of retired LFP batteries has a strong correlation with their internal resistance. This result helped us to propose a rapid and elementary classification method for the calibration of the remaining capacity, and to then formulate a test protocol seeking to balance the time spent and the test cost. Besides, the cut-off voltage and charge-discharge current density have a significant impact on the calibration of the remaining capacity, especially for retired LFP batteries with low residual capacity. In the cycle life test and temperature reliability evaluation process, the results demonstrate that the retired LFP batteries have a good service life when under a lower current of charge/discharge, and the capacity reductions were 2.3%, 11.2% and 4.8% for retired LFP batteries with 80% state of health (SOH), 70% SOH and 60% SOH, respectively, after 500 cycles. Finally, considering the temperature reliability, voltage consistency and large current cycling performance of retired LFP batteries, there are still many challenges in their future echelon utilization.