An Ultrastable Low-Temperature Na Metal Battery Enabled by Synergy between Weakly Solvating Solvents.

The low ionic conductivity and high desolvation barrier are the main challenges for organic electrolytes in rechargeable metal batteries, especially at low temperatures. The general strategy is to couple strong-solvation and weak-solvation solvents to give balanced physicochemical properties. However, the two challenges described above cannot be overcome at the same time. Herein, we combine two different kinds of weakly solvating solvents with a very low desolvation energy. Interestingly, the synergy between the weak-solvation solvents can break the locally ordered structure at a low temperature to enable higher ionic conductivity compared to those with individual solvents. Thus, facile desolvation and high ionic conductivity are achieved simultaneously, significantly improving the reversibility of electrode reactions at low temperatures. The Na metal anode can be stably cycled at 2 mA cm-2 at -40 °C for 1000 h. The Na||Na3V2(PO4)3 cell shows the reversible capacity of 64 mAh g-1 at 0.3 C after 300 cycles at -40 °C, and the capacity retention is 86%. This strategy is applicable to other sets of weak-solvation solvents, providing guidance for the development of electrolytes for low-temperature rechargeable metal batteries.

Bis(2-hydroxyethyl) Terephthalate-Modified Ti3C2Tx/Graphene Nanohybrids as Three-Dimensional Functional Chain Extenders for Polyurethane Composite Films with Strain-Sensing and Conductive Properties.

Incorporation of functional nanofillers can unlock the potential of polymers as advanced materials. Herein, single-layered and three-dimensional reduced graphene oxide (rGO)/Ti3C2Tx (B-rGO@Ti3C2Tx) nanohybrids were constructed using bis(2-hydroxyethyl) terephthalate (BHET) as a coupling agent between rGO and Ti3C2Tx through covalent and hydrogen bonds. It is found that BHET can not only resist the weak oxidization of Ti3C2Tx to some degree but also prevent the self-stacking of Ti3C2Tx and rGO sheets. Then, B-rGO@Ti3C2Tx was used as a functional nanofiller and three-dimensional chain extender for preparing the waterborne polyurethane (WPU) nanocomposite through in situ polymerization. Compared with WPU nanocomposites with an equivalent amount of Ti3C2Tx/rGO@Ti3C2Tx, although containing an equivalent amount of BHET, WPU/B-rGO@Ti3C2Tx nanocomposites show significantly improved performance. For example, 5.66 wt % of B-rGO@Ti3C2Tx endows WPU with a high tensile strength of 36.0 MPa (improved by 380%), thermal conductivity of 0.697 W·m-1·K-1, electrical conductivity of 1.69 × 10-2 S/m (enhanced by 39 times), good strain-sensing behavior, electromagnetic interference (EMI)-shielding performance of 49.5 dB in the X-band, and excellent thermal stability. Therefore, the construction of rGO@Ti3C2Tx nanohybrids with the aid of chain extenders may unlock new possibilities of polyurethane as smart materials.

Fixed-Time Pinning Common Synchronization and Adaptive Synchronization for Delayed Quaternion-Valued Neural Networks.

This article focuses on the fixed-time pinning common synchronization and adaptive synchronization for quaternion-valued neural networks with time-varying delays. First, to reduce transmission burdens and limit convergence time, a pinning controller which only controls partial nodes directly rather than the entire nodes is proposed based on fixed-time control theory. Then, by Lyapunov function approach and some inequalities techniques, fixed-time common synchronization criterion is established. Second, further to realize the self-regulation function of pinning controller, an adaptive pinning controller which can adjust automatically the control gains is developed, the desired fixed-time adaptive synchronization is achieved for the considered system, and the corresponding criterion is also derived. Finally, the availability of these results is tested by simulation example.

Probing the separation mechanism of solid-liquid components in oily sludge and sludge containing polymers for a harmless treatment process of sludge.

In this study, the compositions of oily sludge and sludge containing polymers were analyzed. Sludge was separated preliminarily by conditioning centrifugal technology, whereby the temperature of the centrifugal process and the amount of oil/water separating agent were optimized. Thermal decomposition technology was combined in order to achieve the efficient treatment of sludge. The results showed that the compositions of oily sludge and sludge containing polymers were complex. Therefore, they could not meet the requirements of environmental protection only by conditioning centrifugal technology. After optimization, the best conditioning centrifugal temperature was 70 °C and the content of the oil/water separating agent was 2%. The high efficiency treatment of oily sludge and sludge containing polymers could be realized by combining conditioning centrifugal technology with the thermal decomposition technology. It is found that the sludge could meet the requirements of environmental protection after this combined treatment. This technology has strong adaptability to different types of oilfield sludge. This work is of great significance for the efficient treatment of oily sludge and sludge containing polymers and for environmental protection.

Efficient adsorption of Pb(II) by sodium dodecyl benzene sulfonate intercalated calcium aluminum hydrotalcites: kinetic, isotherm, and mechanisms.

Two novel adsorbents of CaAl-LDHs and sodium dodecyl benzene sulfonate (SDBS) intercalated CaAl-LDHs (SDBS-CaAl-LDHs) were successfully prepared by co-precipitation. The main composition and physical properties of two samples were characterized by XRD, XPS, FT-IR, TG, and SEM. Batch adsorption experiments were conducted to study the effect of pH, adsorption time, and initial concentration of Pb2+. The results showed that the prime adsorption conditions obtained were pH of 5.2 after 60 min with the initial concentration of 300 mg g-1 for CaAl-LDHs and 350 mg g-1 for SDBS-CaAl-LDHs. At 303 K, the adsorption capacities and removal rates of CaAl-LDHs and SDBS-CaAl-LDHs were found to be 456.05 mg g-1, 91.21% and 682.26 mg g-1, 97.47%, respectively. For CaAl-LDHs, the kinetic data for Pb2+ was best fitted with pseudo-2nd-order model, and the adsorption isotherms followed Langmuir and Freundlich isotherm model. The adsorption data of SDBS-CaAl-LDHs can be best described by the pseudo-second-order kinetic and Langmuir model. The Pb2+ adsorption mechanism on SDBS-CaAl-LDHs was explored by XRD, XPS, and SEM, and the important roles of the electrostatic attraction, precipitation, complexation, and ion exchange were demonstrated. The Langmuir adsorption capacities for SDBS-CaAl-LDHs were 797.63, 828.76, and 854.29 mg g-1 at 293 k, 303 k, and 313 k, respectively. Thus, SDBS-CaAl-LDHs may be a highly economical adsorbent for the treatment of contaminated water.

A mitochondria-targeting nitroreductase fluorescent probe with large Stokes shift and long-wavelength emission for imaging hypoxic status in tumor cells.

Development of a mitochondria-targeting fluorescent probe with large Stokes shift and long-wavelength emission was benefit for accurate detection of hypoxic status, which was known as a major factor of the tumor physiology and influence important pathological processes. However, an efficient optical approach for simultaneously achieving such merits was still lacking. In this work, a turn-on fluorescence probe (HBT-NP) was designed to assess the hypoxic condition of tumor cells by detecting nitroreductase (NTR). Probe HBT-NP was constructed by conjugating 4-nitrobenzyl moiety as reaction site for NTR to 2-(benzo[d]thiazol-2-yl)-4-methylphenol derived fluorescent dye HBT-Py which demonstrated large Stokes shift (Δλ = 243 nm) and long wavelength emission (λem = 640 nm) due to intrinsic mechanism of ESIPT together with ICT process. Upon incubated with NTR, HBT-NP could successively undergo nitro reduction reaction and then release HBT-Py. The reaction mechanism was further confirmed by mass spectra and HPLC analysis, and the docking calculation also indicated that the binding mode and docking affinity of probe HBT-NP with NTR play an important role in catalytic reduction reaction process. As a result, HBT-NP displayed a wide linear range (0.1-1.5 µg/mL) and low detection limit (2.8 ng/mL) response to NTR, and could be used to evaluate hypoxic condition of cancer cells with precise mitochondria-targeting.

Highly efficient removal of Cr(VI) from water based on graphene oxide incorporated flower-like MoS2 nanocomposite prepared in situ hydrothermal synthesis.

An efficient adsorbent for the treatment of Cr(VI) was simply fabricated by combining graphene oxide with MoS2 nanosheets via in situ hydrothermal process with CTAB as the surfactant. The experimental results indicated that the agglomeration of the MoS2 nanosheets are reduced and uniformly grown on the graphene sheet during the in situ hydrothermal process, and the introduction of graphene oxide provided higher specific surface area and abundant oxygenic groups. Based on this, the removal efficiency of Cr(VI) onto MoS2/rGO was 75.9% at pH 2.0, which was higher than that of bulk MoS2 (61.0%). On account of Sips adsorption isotherm model, the highest uptake capacity of MoS2/rGO toward Cr(VI) reached 80.8 mg g-1. The adsorption kinetic consequences showed that the chemisorption process was the control step, and the removal mechanism for Cr(VI) is redox and adsorption; in this way, the adsorbed Cr(VI) was partially reduced to Cr(III). Furthermore, this as-prepared adsorbent also presented satisfying reusability for removal of Cr(VI) and can be used for the selective removal of Cr(VI) in the presence of NO3-. In short, it may provide a potential route to enhance the adsorption property of MoS2 toward heavy metals through incorporating with GO, which would expand the applications of MoS2 in the field of treatment of the heavy metal wastewater.

Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: common gene sequence variation and functional characterization.

Betaine-homocysteine methyltransferase (BHMT) catalyzes the remethylation of homocysteine. BHMT2 encodes a protein 73% identical in amino acid sequence to BHMT, but the function of BHMT2 remains unclear. We set out to identify and functionally characterize common genetic variation in BHMT and BHMT2. Specifically, we sequenced exons, exon-intron splice junctions and the 5'-flanking regions (5'-FRs) of BHMT and BHMT2 using 240 DNA samples from four ethnic groups. Twenty-five single nucleotide polymorphisms (SNPs), including 4 nonsynonymous SNPs, and 39 SNPs, including 4 nonsynonymous, were observed in BHMT and BHMT2, respectively. BHMT wild type (WT) and variant allozymes were expressed in COS-1 cells. Variant allozymes showed no significant differences from WT in levels of enzyme activity or immunoreactive protein, but there were statistically significant differences in apparent K(m) values. Luciferase reporter gene constructs were created for the three most common BHMT 5'-FR haplotypes, and significant variation was observed in the ability of these constructs to drive transcription. Although BHMT2 mRNA has been observed in human liver and kidney, expression of the protein has not been reported. We were unable to express BHMT2 in mammalian cells, and the protein aggregated after bacterial expression. Furthermore, BHMT2 was rapidly degraded in a rabbit reticulocyte lysate, but it could be stabilized by cotransfection of COS-1 cells with BHMT and, after cotransfection, it coprecipitated with BHMT. These studies have defined common genetic variation in BHMT and BHMT2 and functionally characterized BHMT SNPs. They may also help to explain why BHMT2 has not previously been defined functionally.