Environmental Science-Nano
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2022
·Vol. 9
·期 7
·2559-2571
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IF 9.473
Meng Li,Mengwen Xu,Quanyu Shi,Haotian Wang,Hongmin Guo,Lidong Wang,Tony D. James
The shortage of freshwater resources caused by heavy metal pollution is an acute global issue. Herein, a novel nanoplatform was fabricated by hydrothermal deposition of 3D-MoS2 nanospheres onto biocompatible wood sponge (WS) for Hg(II) removal. Moreover, a secondary water purification strategy was investigated to produce drinkable water using the exhausted wood sponge. The exhausted MoS2-wood sponge (MWS) was used to construct a solar steam generator by wrapping with a hydrophilic polyvinyl alcohol (PVA) layer to prevent heavy metal ion leakage and to enhance the hydrophilicity. The energy conversion efficiency of the evaporator was calculated to be 95.48% under one sun illumination. Remarkably, the treatment of model desulphurization wastewater from power plants with this functional wood sponge could efficiently reduce the mercury concentration below the limit proposed by the World Health Organization for drinking water. These results provide a basis for the application of upcycled hazardous adsorbents for the purification of drinkable water.
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PROTEOMICS
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2022
·
IF 5.393
Zhouxian Li,Qi Wang,Keyun Wang,Weibing Zhang,Mingliang Ye
Protein lysine monomethylation is an important post-translational modification participated in regulating many biological processes. There is growing interest in identifying these methylation events. However, the introduction of one methyl group on lysine residues has negligible effect on changing the physical and chemical properties of proteins or peptides, making enriching and identifying monomethylated lysine (Kme1) proteins or peptides extraordinarily challenging. In this study, we proposed an antibody-free chemical proteomics approach to capture Kme1 peptides from complex protein digest. By exploiting reductive glutaraldehydation, 5-aldehyde-pentanyl modified Kme1 residues and piperidine modified primary amines were generated at the same time. The peptides with aldehyde modified Kme1 residues were then enriched by solid-phase hydrazide chemistry. This chemical proteomics approach was validated by using several synthetic peptides. It was demonstrated that it can enrich and detect Kme1 peptide from peptide mixture containing 5000-fold more bovine serum albumin tryptic digest. Besides, we extended our approach to profile Kme1 using heavy methyl stable isotope labeling by amino acids in cell culture (hmSILAC) labeled Jurkat T cells and Hela cells. Totally, 29 Kme1 sites on 25 proteins were identified with high confidence and 11 Kme1 sites were identified in both two types cells. This is the first antibody-free chemical proteomics approach to enrich Kme1 peptides from complex protein digest, and it provides a potential avenue for the analysis of methylome.
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Journal of Energetic Materials
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2022
·
IF 2.421
Xiaopeng Zhang,Yige Wu,Pengcheng Wang,Qiuhan Lin,Shusen Chen,Shaohua Jin,Yuangang Xu,Ming Lu
As a new structural motif, an interesting 3D energetic metal – framework of silver ions and 3,4-diaminofurazan, [Ag+(daf)NO3−]n, is successfully synthesized and the structure is determined by single-crystal X-ray diffraction. The effects of hydrogen bond, coordination bond, adsorption and filling interactions make this compound have a high density (2.694 g·cm−3 at 293 K). The calculated detonation velocity and the sensitivities are all comparable with trinitrotoluene (TNT). The onset decomposition temperature is equal to hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), state-of-the-art explosive. This framework provides a potential superiority of E-MOFs for energetic materials.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
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IF 5.518
Yun Xue,Jiaqi Chen,Peng Liu,Jianzhang Gao,Yunyang Gui,Wanting Cheng,Fuqiu Ma,Yongde Yan
In order to satisfy the increasing needs for sustainable development of the nuclear energy industry, it is critical to vigorously develop efficient materials for uranium separation and recovery from wastewater. In this work, novel amidoxime-functionalized membranes (PAO membranes) were successfully synthesized via a facile one-step non-solvent induce phase separation rather than as-reported synthesized approaches that needed complicated additives or harsh reaction conditions. The pore channels provided large specific surface areas and massive binding sites, and the bulk-shape membrane was convenient for collection. Removal of uranium as a function of initial pH, reaction time, initial concentrations of U(VI), and temperature was studied. The maximum adsorption capacity of the PAO membranes toward U(VI) calculated from the Langmuir model was up to 641.72 mg·g −1 at pH 5 and 298 K. Thermodynamic studies indicated that the enrichment of U(VI) was a spontaneous and endothermic process. The removal percentage of uranium reached 86.50% in simulated wastewater in the case of multiple coexisting metal ions . In addition, the scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) results confirmed that the abundant adsorption sites of the PAO membranes were responsible for the efficient immobilization of uranium by forming chelating species, especially amidoxime groups and carboxyl groups. This work presents a novel strategy for mass production of a new generation of high-efficiency adsorbents for uranium-containing wastewater treatment in the future.
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Metals
·
2022
·Vol. 12
·期 4
·579
·
IF 2.695
Wanyi Zeng,Lei Xu,Qiongling Wang,Chen Chen,Minglai Fu
Considering environmental friendliness and economic factors, the separation and extraction of indium under acidic conditions are of great significance. In this research, metal-organic frameworks (MOFs) of UiO-66 were successfully prepared and used for the separation and adsorption of indium. The properties of UiO-66 were structurally characterized using powder X-ray diffraction (XRD), Fourier-Transform Infrared Spectroscopy (FTIR), Brunauer-Emmett-Teller surface area analyzer (BET), thermogravimetric analysers (TGA) and Scanning Electron Microscope (SEM). The results show that UiO-66 can resist acid and keep its structure unchanged, even at a strong acidity of pH 1. The adsorption performance of UiO-66 to indium (III) was also evaluated. The results show that the adsorption process of indium ions was by the Langmuir adsorption isotherm, with a maximum adsorption capacity of 11.75 mg·g−1being recorded. The adsorption kinetics experiment preferably fits the second-order kinetic model. A possible mechanism for the adsorption of In(III) by UiO-66 was explored through X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared analysis(FT-IR). It was concluded that the C=O of free –COOH of UiO-66 was involved in the adsorption of In(III) by cation exchange. This study indicates, for the first time, that UiO-66 can be applied as an acid-resistant adsorbent to recover indium (III).Keywords:UiO-66;MOFs;Adsorption;Indium recovery
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Acta Metallurgica Sinica-English Letters
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2022
·Vol. 35
·期 10
·1653-1664
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IF 3.024
Xie Shenghui,Liao Xiang,Zeng Xierong,Yang Haipeng,He Liang
High-entropy alloys (HEAs) have attracted widespread attention due to their excellent mechanical properties. However, their functional properties arising from the supersaturated solid solution state can be improved. Advanced oxidation processes (AOPs) are considered to be an effective method for decomposing organic pollutants, and HEAs are proposed as effective candidates for AOP catalysts. Currently, several HEAs used for organic pollutant degradation are prepared through mechanical alloying. In this work, FeAlCoNi and FeAlCoNiB Fenton-like catalysts were prepared by single roll melt spinning and subsequent ball milling techniques. We found that the FeAlCoNiB HEA exhibits highly efficient degradation for p -nitrophenol ( p -NP). The degradation efficiency of FeAlCoNiB is 120 times higher than that of FeAlCoNi, which confirms that boron functions effectively during the degradation process. FeAlCoNiB has a better degradation efficiency than pure iron powder and a degradation efficiency comparable to that of the amorphous Fe 78 Si 11 B 11 alloy. Additionally, the degradation efficiency of FeAlCoNiB X increases ( k values from 0.13 to 0.55 min −1 ) when the boron content increases from an X value of 0.25 to 1.25. We speculate that Fe 2 B favors the degradation process and promotes zero-valent iron to decompose organic pollutants through a galvanic cell effect. Possible p -NP degradation pathways are proposed after LC–MS analysis. This study provides a new series of HEA Fenton-like catalysts, which have the potential to be prepared into bulk devices for industrial applications.
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Journal of Materials Chemistry B
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2022
·Vol. 10
·期 21
·4012-4019
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IF 7.571
Zhen Zhao,Hua Zhang,Hongda Chen,Yuanhong Xu,Lina Ma,Zhenxin Wang
In this work, the polyacrylamide/phytic acid/polydopamine (termed as PAAM/PA/PDA) hydrogel is used as a drug loading matrix and photothermal conversion reagent, which is prepared by copolymerization of dopamine with acrylamide through a phytic acid crosslinker. Due to the porous structure of PAAM and strong near-infrared light (NIR)-absorption of PDA, the PAAM/PA/PDA hydrogel exhibits a high doxorubicin (DOX)-loading capacity (170 mg g−1) and efficient photothermal transduction efficiency (47.4%) even under low power density 808 nm NIR laser (0.75 W cm−2) irradiation, which is superior to those of most conventional photothermal conversion agents reported in the literature. With NIR laser irradiation, the PAAM/PA/PDA hydrogel loaded with DOX (termed as PAAM/PA/PDA/DOX) shows excellent synergistic interaction between photothermal therapy (PTT) and enhanced chemotherapy, resulting in the completely suppressed growth of mouse-bearing SW620 tumors. Furthermore, the PAAM/PA/PDA hydrogel shows good physicochemical stability, negligible cytotoxicity and low toxicity in vivo. All these characteristics render the as-prepared PAAM/PA/PDA hydrogel promising for biomedical applications.
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RSC Advances
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2022
·Vol. 12
·期 13
·7950-7960
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IF 4.036
Chuanxiang Zhang,Xiqiang Li,Lingling Ding,Chen Jin,Haijun Tao
Perovskite solar cells (PSCs) are considered to be ideal energy devices, where perovskite-type organic metal halides act as light-absorbing materials. In PSCs, the photoexcitons are extracted and separated to afford high photoelectric conversion efficiency under the action of the built-in electric field (Ebi). However, the current challenge is that a low Ebi cannot provide a sufficient driving force to separate photonic excitons, which causes the captured charges to escape from the deep energy-level defect state. Here, the ferroelectric material barium titanate (BaTiO3) was directly introduced into the perovskite precursor solution to reduce the defection density (to 8.58 × 1017 cm−3) in PSCs and promote the separation of photoexcitons. Furthermore, the addition of BaTiO3 improved the quality of the perovskite film and significantly increased the photoelectric performance after the polarization treatment. This is mainly attributed to the residual polarization electric field generated by ferroelectric polarization, which increased the Ebi of the PSCs and the width of the depletion layer and inhibited the non-radiative recombination of carriers. This work provides a possibility to design and develop optoelectronic devices with high-efficiency optoelectronic response behavior.
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Journal of Materials Chemistry C
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2022
·Vol. 10
·期 13
·5147-5154
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IF 8.067
Yanbin Chen,Hewei Yang,Jian Song,Bao Zhang
Doping metal ions into a perovskite lattice is an effective strategy for tailoring the intrinsic properties of perovskite nanocrystals (NCs). Herein, strong red-emitting and highly ambient and light stable Fe2+-doped CsPbBrI2 NCs with a maximum photoluminescence quantum yield (PLQY) of 92.1% were obtained. Systematic investigation of Fe2+ doping on the stability and the luminescence performance of CsPbBrI2 NCs was performed. Owing to the smaller ionic size compared to Pb2+, Fe2+ induced the lattice contraction and shortened the bond length of Pb–X, which suppressed the distortion of [PbX6]4− octahedra, thus improving the stability of CsPbBrI2 NCs. The champion sample could maintain up to 86% emission under the ambient conditions for 5 weeks. Besides, the incorporation of Fe2+ suppressed the formation of halide vacancies and optimized the relaxation process of CsPbBrI2, thereby contributing to the enhancement of PLQY. This facile Fe2+ doping method provides an effective strategy to synthesize stable and highly photoluminescent red perovskite materials.
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EUROPEAN JOURNAL OF PHARMACOLOGY
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2022
·
IF 5.195
Fangfang Xu,Jun Wang,Pan Wang,Tao Hou,Han Zhou,Yaopeng Zhao,Jixia Wang,Yanfang Liu,Xinmiao Liang
Ursodeoxycholic acid (UDCA) is a safe bile acid effective in reducing hepatic steatosis in non-alcoholic fatty liver disease (NAFLD). However, the mechanism of action linked to this effect is poorly defined. In the present study, we identified that UDCA acted as a free fatty acid receptor 4 (FFA4) agonist with EC 50 of 10.4 ± 0.7 μM, and its activity was determined by dynamic mass redistribution, fluorometric imaging plate reader, inositol monophosphate and bioluminescence resonance energy transfer assays. Moreover, UDCA showed FFA4 selectivity over eleven other G protein-coupled receptors. Real-Time PCR and immunocytochemistry analyses showed that FFA4 was abundantly expressed in human hepatocytes HuH-7 cells. In an in vitro model of NAFLD induced by oleic acid (OA), UDCA downregulated lipid accumulation in HuH-7 cells and suppressed sterol-regulatory element binding protein-1c (SREBP-1c) mRNA expression. This suppression of SREBP-1c was restored when FFA4 expression was knocked down in siRNA assay. In a mouse model of hepatic steatosis, db/db mice were exposed to a high-fat diet (HFD), and treatment of UDCA or docosahexaenoic acid (DHA, an endogenous FFA4 agonist) effectively prevented body weight gain and hepatic fat deposition and reduced triglyceride (TG) levels in serum and liver. This study not only identified a new skeleton of FFA4 agonists, but also demonstrated that FFA4 signal was accounting for the protective effects of UDCA in the NAFLD treatment.
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Petroleum Science
·
2022
·
IF 4.757
Xiao-Yi Liu,Xiu-Ping Li,Rong-Xiang Zhao
Ce 2 (MoO 4 ) 3 was synthesized by a simple reflux method using cerium nitrate hexahydrate and ammonium molybdate as reactants. The as-prepared Ce 2 (MoO 4 ) 3 was characterized by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Scanning electron microscope (SEM), and X-ray photoelectron spectroscopy (XPS). The removal of dibenzothiophene (DBT) in model oil was studied using Ce 2 (MoO 4 ) 3 as catalyst and oxygen as oxidant. The reaction factors such as reaction temperature, amount of catalyst, and sulfide type on sulfur removal were researched. The results prove that both Ce 3+ and MoO 4 2- play significant role in the conversion from DBT to DBTO 2 . The Ce 2 (MoO 4 ) 3 catalyst has an excellent performance for the sulfur removal of DBT. Under the optimum reaction conditions, sulfur removal of 99.6% was obtained. After recycling five times, no significant loss in catalyst activity of Ce 2 (MoO 4 ) 3 . Mechanism of aerobic oxidative desulfurization was proposed based on the experiment of free radical capture and infrared characterization.
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ELECTROPHORESIS
·
2022
·
IF 3.595
Yulan Liu,Ling Xia,Xiaohua Xiao,Gongke Li
Microfluidic CE (MCE) is an effective solution for rapid and sensitive determination of multiple analytes. Herein, a dynamic coated cyclic olefin copolymer microchip was developed having an on-chip micropump for fluid velocity adjusting in electrophoretic separations. This micropump was fabricated by constructing a polyacrylamide gel membrane at one channel terminal. Once applying electric field across the membrane, a pressure-driven flow generated automatically to balance the electroosmotic flow (EOF) mismatch at the channel-membrane interface. The influence of gel precursor concentration and operating voltages on the fluid velocity was carefully evaluated. Moreover, the highly integration of injection, separation, and pumping units of the MCE system minimized the dead volume and provides satisfied column efficiency. Experiments showed that by adjusting of pumping voltage reduced the fluid velocity by a factor of 6, resulting six- and threefold resolving power enhancements of rhodamine dye mixture and amino acid mixture, respectively. Furthermore, the developed MCE method was applied for rhodamines and amino acids quantitation in food and cosmetics, with standard addition recoveries of 87.3–106.9% and 89.9–117.4%, respectively. These results were also confirmed by standard HPLC method, revealing the application potential in fast and onsite analysis of complex samples.
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