JOURNAL OF MATERIALS RESEARCH
·
2014
·Vol. 29
·期 24
·2934-2941
·
IF 1.815
Hongxu Guo,Di Guo,Zishan Zheng,Weng Wen,Jianhua Chen
Zn3(VO4)2 nanorods with visible light-driven photocatalytic activity were prepared by hydrothermal reaction and characterized by x-ray diffraction, Fourier transform infrared, scanning electron microscopy, x-ray photoelectron spectroscopy, UV–vis diffuse reflectance spectra, and Brunauer–Emmett–Teller surface area and pore size analyzer. The Zn3(VO4)2 nanorods consisted of rods with a thickness of approximately 30 nm, length in the range 400–600 nm, and width in the range 150–250 nm. The photocatalytic degradation activities for methylene blue (MB) and 4-nitrophenol (4-NP) over the Zn3(VO4)2 nanorods were studied in detail. The photocatalytic activity of the as-prepared photocatalyst for MB and 4-NP in visible light under the same conditions was about 3.5 times and 2.5 times higher than that of N–TiO2, respectively. The main active species in the photodegradation come from •OH, and the photogenerated electrons also partly involved in the photocatalytic degradation process, in which the •OH radicals formed were in proportional to the light illumination time obeying zero-order reaction rate kinetics.
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Scientific Reports
·
2015
·Vol. 5
·期 1
·1-14
·
IF 5.578
Liao Hanpeng,Zheng Haiping,Li Shuixian,Wei Zhong,Mei Xinlan,Ma Hongyu,Shen Qirong,Xu Yangchun
A multiple xylanase system with high levels of xylanase activity produced from Penicillium oxalicum GZ-2 using agricultural waste as a substrate has been previously reported. However, the eco-physiological properties and origin of the multiplicity of xylanases remain unclear. In the present study, eight active bands were detected using zymography and all bands were identified as putative xylanases using MALDI-TOF-MS/MS. These putative xylanases are encoded by six different xylanase genes. To evaluate the functions and eco-physiological properties of xylanase genes, xyn10A , xyn11A , xyn10B and xyn11B were expressed in Pichia pastoris . The recombinant enzymes xyn10A and xyn10B belong to the glycoside hydrolase (GH) family 10 xylanases, while xyn11A and xyn11B belong to GH11 xylanases. Biochemical analysis of the recombinant proteins revealed that all enzymes exhibited xylanase activity against xylans but with different substrate specificities, properties and kinetic parameters. These results demonstrated that the production of multiple xylanases in P. oxalicum GZ-2 was attributed to the genetic redundancy of xylanases and the post-translational modifications, providing insight into a more diverse xylanase system for the efficient degradation of complex hemicelluloses.
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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY
·
2024
·Vol. 333
·期 6
·2691-2696
·
IF 1.5
Wang Yi,Yang Jiajia,Sui Jixue,Wang Lan,Tang Jia,Yang Yu,Lu Yunyun,Dai Shuang,Cao Qi
Efficient separation of europium (Eu) from aqueous solution is pivotal for the sustainable development of nuclear industry and rare earth industry. In this work, bis(2-ethylhexyl) phosphate (P204) was employed to separate Eu(III) by solvent extraction method using kerosene as diluent. The extraction equilibrium could reach within 30-min contact time. The extraction ratio enhanced as the increased O:A phase ratio, extractant concentration, and temperature. However, the HCl introduction caused its clear descent. Combined with the slope method and FT-IR analysis, extraction mechanism could be unveiled, which is the coordination between P=O double bond and Eu(III) ions in a proportion of 3:1.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2024
·
IF 7.7
BingBing Wang,Jian-Zhong Xu,Shuai Liu,Zhi-Ming Rao,Wei-Guo Zhang
L-Tryptophan hydroxylation catalyzed by tryptophan hydroxylase (TPH) presents a promising method for synthesizing 5-hydroxytryptophan (5-HTP), yet the limited activity of wild-type human TPH2 restricts its application. A high-activity mutant, MT10 (H318E/H323E), was developed through semi-rational active site saturation testing (CAST) of wild-type TPH2, exhibiting a 2.85-fold increase in k cat / K m over the wild type, thus enhancing catalytic efficiency . Two biotransformation systems were developed, including an in vitro one-pot system and a Whole-Cell Catalysis System (WCCS). In the WCCS, MT10 achieved a conversion rate of only 31.5 % within 32 h. In the one-pot reaction, MT10 converted 50 mM L-tryptophan to 44.5 mM 5-HTP within 8 h, achieving an 89 % conversion rate, outperforming the M1 (NΔ143/CΔ26) variant. Molecular dynamics simulations indicated enhanced interactions of MT10 with the substrate, suggesting improved binding affinity and system stability. This study offers an effective approach for the efficient production of 5-HTP.
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RADIATION PHYSICS AND CHEMISTRY
·
2024
·
IF 2.8
Qin Wen,Shizong Wang,Jianlong Wang,Hai Chen,Yuedong Zhou
In this study, the degradation and mineralization of 2-chlorobiphenyl (2-PCB) by gamma irradiation were investigated in the presence of persulfate (PS), to examine the synergistic effect of radiation and persulfate oxidation. The results showed that the absorbed dose required for complete removal of 2-PCB decreased in the presence of PS. In addition, compared to a single irradiation system, the removal efficiency and mineralization of 2-PCB in deionized water , groundwater, and secondary effluent increased when irradiation combined with PS. 2-PCB at concentration of 4 mg L −1 to 8 mg L −1 could be efficiently degraded at a wide pH range (3.0–9.5) in irradiation-activated PS (irradiation/PS) system. The presence of 10 mM or 100 mM of Cl − , NO 3 − , CO 3 2− , and SO 4 2− in irradiation/PS system had no obvious influence on 2-PCB removal. 2-PCB was degraded under the combined action of sulfate radicals (SO 4 •− ) and hydroxyl radicals (·OH), in which ·OH contributed more. The irradiation/PS system is promising to treat PCB-containing wastewater.
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MACROMOLECULAR CHEMISTRY AND PHYSICS
·
2024
·Vol. 225
·期 19
·2400159
·
IF 2.5
Yuxiao Li,Wentao Liu,Kan Liu,Qingyue Wang,Xiaohui Li,Erlita Mastan,Yuanfeng Wu,Pingwei Liu,Bo Peng,Khak Ho Lim,Wen-Jun Wang
Mechanistic understanding of free radical polymerization (FRP) in aqueous solution is hindered by the lack of kinetic coefficient data. Here, we investigated the propagation rate coefficient ( k p ) for FRP of HEMA in aqueous solution. The k p at 80 °C increased by 6 times as the monomer weight fraction in aqueous system decreases from 100 wt.% to 6 wt.%, that is., from 6.0 × 10 3 to 3.3 × 10 4 L·moL −1 ·s −1 . This increase in k p is associated with the increase in pre-exponential factor ( A ), which suggests an increase in entropy with increasing water molecules in the polymerization system. To investigate the effect of solvent on k p , pulse-laser polymerization in solvents of different hydrogen bonding affinity, that is, 50 wt.% butyl propionate (BP) and dimethyl formamide (DMF), are conducted. The k p obtained are in order of k p , bulk ∼ k p , BP > k p , DMF , suggesting that the intermolecular hydrogen bonding at carbonyl moieties critically affects the geometry of transition state quasi-equilibrium in propagation. We underpinned this observation by analyzing the carbonyl and alkene moieties of HEMA in different solvents using infrared (IR) spectroscopy. The mechanistic analyses and insights relating to hydrogen bonding and functional moieties can be relevant for future studies involving non-aqueous solvents promoting hydrogen bonds.
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INTERNATIONAL JOURNAL OF THERMOPHYSICS
·
2024
·Vol. 45
·期 7
·1-14
·
IF 2.5
Almasi Mohammad
A thorough evaluation of the thermophysical properties of ethylcyclohexane (ECH) mixed with 2-alkanols (2-propanol to 2-hexanol) is presented across the temperature range of 293.15 to 323.15 K. The focus of this study is on the density and viscosity behavior of these systems. The experimental results demonstrate positive deviations from ideality in excess molar volume, while viscosity deviations are negative for all examined mixtures. This observation suggests the presence of weak intermolecular interactions between ECH and the 2-alkanol. These findings are consistent with the self-association behavior of 2-alkanol and the nonpolar nature of ECH, which disrupts the associated structures of the alcohols. Furthermore, the Friction theory ( f-theory ) was employed to model the viscosity of the binary mixtures. The f-theory exhibits excellent agreement with the experimental data, with a maximum deviation of only 2.24% observed in the ECH + 2-butanol system. This minimal discrepancy underscores the f-theory's efficacy in accurately correlating the viscosity measurements.
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CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Yetong Li,Kailong He,Siyuan Zhao,Linyu Jiao,Huiyong Chen,Xiaoxun Ma,Chengyi Dai
Many researchers have extensively studied the alkylation of naphthalene with methanol for the preparation of high-value-added chemicals, especially methylnaphthalenes (MNs). Studies indicated that methanol generates a large number of methanol-to-olefin by-products on zeolites, resulting in low selectivity of the target product and poor stability of the catalyst, limiting its application in the industrial field. In this study, CO 2 hydrogenation was coupled with naphthalene alkylation, and the H 3 CO* active intermediate generated in situ was alkylated with naphthalene by using metal oxide-zeolite (OX-ZEO) bifunctional catalysts, which exhibited the ‘slow release’ phenomenon of the methylation reagent. It improved naphthalene conversion, suppressed deep alkylation and coke deposition side reactions and kept the catalyst stable for up to 500 h. A high-density and medium-strength Brønsted acid center facilitated the efficient migration of H 3 CO* active intermediates with the desorption of 2-methylnaphthalene (2-MN), which was particularly important for improving naphthalene conversion and 2-MN selectivity. The in situ IR showed that more Brønsted acid sites of Ga-S-1 effectively pulled the migration process of H 3 CO* species to the zeolitic acid center and increased the efficiency of C-C coupling compared to ZSM-5, which promoted the alkylation of H 3 CO* species with naphthalene. The results of chemisorption experiments showed that the medium-strength Brønsted acid site, which promoted the desorption of 2-MN, inhibited the deep alkylation reaction. The 2,6-dTBPy-IR results showed that the presence of fewer Brønsted centers on the outer surface of Ga-S-1 further optimized the product distribution and enhanced the selectivity of 2-MN in MNs to more than 90 %. Under optimal conditions, 80.1 % selectivity for MNs was obtained via ZnZrO x &Ga-S-1 bifunctional catalysts, with 97.4 % selectivity for 2-MN in MNs.
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SCIENCE OF THE TOTAL ENVIRONMENT
·
2025
·
IF 8
Yiming Sun,Ruili Zhang,Jiali Li,Yihan Hu,Haolin Zhang,Xiangjie Wang,Yi Yang,Haibin Wang,Ming Ge
2-Ethylhexyl diphenyl phosphate (EHDPHP) is a widely used organophosphorus flame retardant and plasticizer easily released into the environment. Its biological toxicity is of great concern. The lung is considered a possible target organ for EHDPHP, but currently, there are limited studies on the biotoxicity of EHDPHP in poultry lungs. Therefore, the lungs were selected as the target organ to study the toxic effects of EHDPHP on chicks and their mechanisms of action. In this study, 7-day-old chicks were gavaged with different concentrations of EHDPHP, and lung samples were collected at 14, 28, and 42 days after intragastric administration. Lung histopathological and ultrapathological changes were examined by paraffin section-HE staining and transmission electron microscopy. The levels of lung damage markers (LDH) and oxidative stress markers (GSH-Px, SOD, and MDA) were detected by applying the kit. In contrast, lung cell pyroptosis-related factors (NLRP3, ASC, NF-κB, Pro-Caspase-1, IL-18, and IL-1β) and inflammatory factors (IL-6 and TNF-α) were assessed by using the qRT-PCR, Western blot and ELISA techniques. The results showed that EHDPHP induced pathological morphological changes and elevated LDH content in chick lungs, decreased lung antioxidant enzymes (GSH-Px and SOD) activities, increased peroxidation product MDA content and up-regulated the expression levels of cellular pyroptosis factors (NLRP3, ASC, NF-κB, Pro-Caspase-1, IL-18, and IL-1β), and the synthesis and secretion of inflammatory factors (IL-6 and TNF-α) were promoted. The above changes were EHDPHP dose-dependent. The results indicated that EHDPHP induced oxidative stress in chick lungs, resulting in oxidative damage to the lungs, and, intriguingly, the cellular pyroptosis pathway was activated, which was also involved in the process of EHDPHP-induced inflammatory damage in chick lungs. The results of this study revealed for the first time the damaging effects and mechanisms of EHDPHP on chick lungs. Also, they provided a scientific basis for further exploring the mechanisms of toxicity damage, safe use, and pollution control of EHDPHP.
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BIOSENSORS & BIOELECTRONICS
·
2024
·
IF 10.7
Yanpei Xu,Haoyu Wu,Meng Sun,Hongyu Song,Chuxiao Sun,Fudong Jia,Qi Wang
In the detection of biomolecules, surface plasmon resonance (SPR) sensors require high sensitivity. In this study, we propose a sensitivity-enhanced functionalized plasmonic interface based on Ag–TiO 2 –Co(OH) 2 nanosheets structure. Compared to unmodified SPR sensors, the sensitivity of the sensor decorated with TiO 2 and Co(OH) 2 nanosheets is increased by 130.84%, reaching 5764.27 nm/RIU. This enhancement is attributed to the high refractive index of the coating, as well as the high specific surface area and abundant active sites provided by the synthesized Co(OH) 2 nanosheets with a multi-grooved structure. Additionally, employing a double-antibody sandwich method, the antibody-functionalized plasmonic interface enables specific detection of human serum albumin (HSA). The linear response of this sensor was in the wide range of 0.4–150 μM, and the LOD reached 154.89 nM(K D is approximately 1.73 × 10 −6 M). This novel SPR sensor offers a new strategy for biochemical sensing and provides a highly sensitive platform for immunoassays.
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Cells
·
2025
·Vol. 14
·期 6
·394
·
IF 5.2
Min Jiang,Jiaqi Hou,Qianqian Chai,Shihao Yin,Qian Liu
Pulmonary fibrosis due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is the leading cause of death in patients with COVID-19. β-catenin, a key molecule in the Wnt/β-catenin signaling pathway, has been shown to be involved in the development of pulmonary fibrosis (e.g., idiopathic pulmonary fibrosis, silicosis). In this study, we developed a SARS-CoV-2-infected A549-hACE2 cell model to evaluate the efficacy of the A549-hACE2 monoclonal cell line against SARS-CoV-2 infection. The A549-hACE2 cells were then subjected to either knockdown or overexpression of the effector β-catenin, and the modified cells were subsequently infected with SARS-CoV-2. Additionally, we employed transcriptomics and raw letter analysis approaches to investigate other potential effects of β-catenin on SARS-CoV-2 infection. We successfully established a model of cellular fibrosis induced by SARS-CoV-2 infection in lung-derived cells. This model can be utilized to investigate the molecular biological mechanisms and cellular signaling pathways associated with virus-induced lung fibrosis. The results of our mechanistic studies indicate that β-catenin plays a significant role in lung fibrosis resulting from SARS-CoV-2 infection. Furthermore, the inhibition of β-catenin mitigated the accumulation of mesenchymal stroma in A549-hACE2 cells. Additionally, β-catenin knockdown was found to facilitate multi-pathway crosstalk following SARS-CoV-2 infection. The fact that β-catenin overexpression did not exacerbate cellular fibrosis may be attributed to the activation of PPP2R2B.
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CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Yujing Liu,Qi Liu,Xin Zhou,Xiaohui Liu,Mingyue Li,Zhongqiu Liu,Anguo Ying
Improving the voltage window of aqueous supercapacitors beyond 2.5 V without diminishing their capacitance performance is a big challenge to achieve excellent energy density because of the undesirable water decomposition. Herein, this study developed a novel vanadium phosphate (VPO) of the VO(PO 3 ) 2 aerogel as the electrode to enlarge the device voltage, which could effectively raise HER/OER overpotentials and thus achieving a stable wide electrochemical window of −1 ∼ 1 V (vs. SCE) with remarkably improved capacitance. The VPO microstructure is organized by nanowire-stacked lamellar bricks via engineering a controllable phase-transformation using the V-P-citric acid-aerogel as the precursor. Examined as the supercapacitor electrode, in-situ X-ray powder diffraction analysis uncovers that the VO(PO 3 ) 2 undergoes a reversible phase-transformation reaction associated with Na + intercalation/de-intercalation in Na 2 SO 4 and a typical redox pseudocapacitance process in KOH. For the first time, a 2.8 V symmetric aqueous supercapacitor was further assembled with an energy density of 123.1 Wh kg −1 at the power density of 580 W kg −1 , which is much superior to those of all reported V-base supercapacitors. The underlying mechanisms of the VO(PO 3 ) 2 on ultrahigh voltage window and charge storage are further elucidated, which provide the fundamental guidance for structuring VPO-based electrodes used for commercial energy storage devices.
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