CLINICA CHIMICA ACTA
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2022
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IF 6.314
Jiyun Zhang,Zhizhen Lai,Rui Ding,Jinyu zhou,Zhonghao Yuan,Dan Li,Xuzhen Qin,Jiang Zhou,Zhili li
Background Altered glycosylation modulates the structure and function of disease-related proteins. The associations between serotransferrin (STF) N -glycosylation and liver diseases (LDs) have been revealed. However, how intact N -glycopeptides vary among different types of liver diseases remains unclear. Methods Intact STF N -glycopeptides from patients with chronic liver disease (CLD, n = 92), primary liver cancer (PLC, n = 123), metastatic liver cancer (MLC, n = 57), and healthy controls (HCs, n = 59) were determined using high-resolution mass spectrometry. Results Significant changes were displayed in STF glycosylation among 4 groups. The LD screening model, including Asn432 G1S/G2S, Asn432 G2S/G2S2, and Asn630 G2NS2/G2FNS2, was constructed to differentiate LDs from HCs, with a AUC of 0.92. The liver cancer (LC) diagnostic model, a combination of Asn432 G1-N/G1S-N, Asn432 G1/G2, Asn432 G2FS/G2FS2, and Asn630 G1S-N /G1S, showed good performance in discriminating LC from CLD (AUC = 0.93). Moreover, AFP-negative LC patients (93 %) were successfully predicted by the LC diagnostic model. Furthermore, the MLC triage model, composed of Asn432 G1/G2, Asn432 G3F/G3FS, Asn630 G2/G2S, Asn630 G2S2/G2NS2, and Asn630 G3FS/G3FS2, yielded an AUC of 0.98 between PLC and MLC. Conclusions STF N -glycosylation is a potential biomarker for the accurate classification of different LDs.
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Journal of the American Chemical Society
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2022
·
IF 16.383
Fei Xiao,Yian Wang,Gui-Liang Xu,Fei Yang,Shangqian Zhu,Cheng-Jun Sun,Yingdan Cui,Zhiwen Xu,Qinglan Zhao,Juhee Jang,Xiaoyi Qiu,Ershuai Liu,Walter S. Drisdell,Zidong Wei,Meng Gu,Khalil Amine,Minhua Shao
The poor durability of Pt-based nanoparticles dispersed on carbon black is the challenge for the application of long-life polymer electrolyte fuel cells. Recent work suggests that Fe- and N-codoped carbon (Fe–N–C) might be a better support than conventional high-surface-area carbon. In this work, we find that the electrochemical surface area retention of Pt/Fe–N–C is much better than that of commercial Pt/C during potential cycling in both acidic and basic media. In situ inductively coupled plasma mass spectrometry studies indicate that the Pt dissolution rate of Pt/Fe–N–C is 3 times smaller than that of Pt/C during cycling. Density functional theory calculations further illustrate that the Fe–N–C substrate can provide strong and stable support to the Pt nanoparticles and alleviate the oxide formation by adjusting the electronic structure. The strong metal–substrate interaction, together with a lower metal dissolution rate and highly stable support, may be the reason for the significantly enhanced stability of Pt/Fe–N–C. This finding highlights the importance of carbon support selection to achieve a more durable Pt-based electrocatalyst for fuel cells.
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International Journal of Environmental Science and Technology
·
2023
·Vol. 20
·期 11
·11865-11876
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IF 3.1
Xin X.,Liu H.,Sun J.,Gao K.,Jia R.
The composite material based on N- , S- , and Fe-doped TiO 2 (NSFe-TiO 2 ) synthesized by wet impregnation was used as a photocatalyst to rapidly degrade sulfadiazine. The photocatalytic degradation behavior and mechanism of sulfadiazine on NSFe-TiO 2 were investigated for revealing the role of degradation under ultraviolet light. The results showed that compared with TiO 2 , NSFe-TiO 2 markedly improved the efficiency in photocatalytic degradation of sulfadiazine: more than 90% of sulfadiazine could be removed within 120 min by NSFe-TiO 2 dosage of 20 mg L −1 . The process conformed to first-order reaction kinetics model. The parameters such as loaded amount of NSFe-TiO 2 , solution pH value, humic acid concentration and recycle numbers on removal efficiency were also studied. Compared to neutral and alkaline conditions, acidic condition was not conducive to the photocatalysis. HA, Ca 2+ , Cu 2+ and Zn 2+ in the actual water body had mild inhibition on sulfadiazine degradation in UV/NSFe-TiO 2 system. Fragments screened by high-resolution mass spectrometry were conducted to explore the oxidation mechanism and pathways of sulfadiazine degradation. On the whole, UV/NSFe-TiO 2 photocatalysis has a good effect on sulfadiazine removal.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
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IF 9.9
Tiantian Feng,Zhijie Cui,Pengfei Guo,Xuehong Wang,Juan Li,Xien Liu,Wenpin Wang,Zhongcheng Li
Recent experimental analysis indicates WO 3 -based nanostructures exhibit poor hydrogen evolution reactivity, particularly in alkaline medium, arising from the low electron transfer rate. It is imperative to tune the composition and structure of WO 3 to boost the cleavage of H-OH bond. Here, we construct Ru/WO 3 -W 2 N/N-doped carbon sheets (Ru/WO 3 -W 2 N/NC) using m-WO 3 nanosheets as precursors with the aid of RuCl 3 , Tris (hydroxymethyl) aminomethane, and dopamine. Structural investigation reveals the formation of N-doped carbon sheets, Ru nanoparticles, and WO 3 -W 2 N. As a result, hydrogen evolution reactivity is greatly improved on Ru/WO 3 -W 2 N/N-doped carbon sheets with 64 mV at 10 mA/cm 2 in 1 mol/L (M) KOH, outperforming most of WO 3 -based electrocatalysts in previous literatures. Meanwhile, it facilitates the generation of H 2 in 0.5 M H 2 SO 4 with the excellent activity of 110 mV at 10 mA/cm 2 . Our work provides an efficient strategy to tailor the electronic structure of WO 3 to catalyze acidic and alkaline hydrogen evolution reaction.
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高影响因子
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
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2022
·Vol. 26
·期 7
·e202200489
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IF 2.551
Wenlin Zhang,Tingting He,Shimeng Liu,Lu-Hua Zhang,Fengshou Yu
Graphical Cobalt phthalocyanine was supported on N-doped MXene via axial coordination and π-π stacking. The formed axial coordination configuration N−Co−N 4 can effectively break the planar structure of Co-N 4 and enhance the oxygen reduction performance with an E 1/2 of 0.863 V, which is better than the 20 wt.% Pt/C catalyst of 0.85 V. The precise control of electronic configurations of catalytic sites via molecular engineering is significantly desirable for boosting electrocatalytic activity. We reported a new-type composite electrocatalyst with cobalt phthalocyanine supported on N-doped MXene nanosheets (N-MXene/CoPc) through a self-assembly process. Beneficial from the joint action of N sites participation and axial coordination, N-MXene/CoPc exhibits a high ORR activity with positive onset potential (E onset =0.98 V vs. RHE) and half-wave potential (E 1/2 =0.863 V), which is superior over the pristine CoPc (E 1/2 =0.72 V) and the composite with undoped MXene as support (MXene/CoPc, E 1/2 =0.771 V). Additionally, N-MXene/CoPc exhibits an excellent durability with only 8.5 % attenuation after 25000 s of continuous i-t test, while a more obvious decay 18.6 % for 20 wt.% Pt/C. This work not merely reported a robust ORR catalyst, but more provides a reasonable design strategy for nonnoble-metal catalysts through catalyst-support interactions.
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CHEMICAL ENGINEERING JOURNAL
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2022
·
IF 16.744
Jiangna Xing,Xin Huang,Xin Yong,Xin Li,Jun Li,Jingkang Wang,Na Wang,Hongxun Hao
Metal-free g-C 3 N 4 has received wide attentions because of the economy and environmental friendliness of it. However, the synthesis of simple and efficient g-C 3 N 4 modified materials is still challenging. In this study, series of novel N -doped porous thin-walled g-C 3 N 4 nanotubes (CNx) were synthesized through supramolecular self-assembly and thermal polymerization using melamine and aminourea hydrochloride as raw materials. SEM, XRD, XPS, etc. were used to analyze microscopic morphology and chemical structure of synthesized photocatalysts. PL spectra, EIS Nyquist curves and UV–vis DRS, etc. were applied to study the photoelectrochemical and optical properties. Besides, the performance of the synthesized catalysts was illustrated through TC photodegradation experiments, and the degradation rate of tetracycline (TC) by CN0.75 can reach to 93.0 % and the reaction rate constant was calculated to be 0.1347 min −1 . The excellent photocatalytic activity is primarily related to higher specific surface area and the formation of midgap states after N doped, which is conducive to the separation of charges. Finally, the possible pathways and mechanisms were proposed by determining the degradation intermediates and active species in the TC photodegradation process.
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CHEMICAL ENGINEERING JOURNAL
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2022
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IF 16.744
Yu Jiang,Marhoun Ferhat,Wenhao Fan,Shaoping Chen,Yachao Wang,Jie Chen,Rasha Abdullah Ahmed Al-Yusufi,Chaochao Dun
Additional cation doping is one of the potential strategies to enhance the thermoelectric (TE) performance of Mg 3 Sb 2 -based materials with precise regulation of interaction between cations and the host. In this work, using Mg 3 Sb 1.5 Bi 0.5 as an example, we confirmed that co-doping rare-earth elements with Y and La is capable to simultaneously improve its power factor and suppress the thermal conductivity : Y is an effective n -type dopant to regulate the optimal carrier concentration, while La doping can modulate the band structure and increase the effective mass that related to the improved Seebeck coefficient . A promising power factor of 18.3 μW cm -1 K -2 is obtained after co-doping. Meanwhile, the lattice thermal conductivity is dramatically reduced to 0.39 W m -1 K -1 at 750 K thanks to the extra defect scattering introduced by Y and La. As a result, a peak figure of merit ( zT ) of 1.76 and a competitive average zT of 1.1 among 300–750 K are achieved in Mg 3.2 Y 0.04 La 0.01 Sb 1.5 Bi 0.5 . The synergistic effect stemming from dual-cations doping provides profound insights for controllable host-dopant design and modulation toward high-efficient n-type TE materials .
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FOOD RESEARCH INTERNATIONAL
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2022
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IF 7.425
Yuanfei Ge,Jinyong Wu,Min Pang,Dan Hu,Zhongkui Li,Xiangqin Wang,Lijie Sun,Xiangsong Chen,Jianming Yao
In this study, carboxymethyl chitosan (CMCS) and N - acetylneuraminic acid (NeuAc) were used to develop C-NeuAc hydrogels to encapsulate Pediococcus pentosaceus QK-1. The mechanical properties, thermal stability, in vitro degradation, and pH sensitivity of the hydrogel were evaluated. The C-NeuAc concentration required for optimal hydrogel performance was 3% (w/v). Hydrogel swelling behaviour was effectively assessed by Fickian diffusion and Schott’s second-order kinetic models. The hydrogel demonstrated excellent biocompatibility and low in vitro cytotoxicity. An in vitro assay revealed that the viability of Pediococcus pentosaceus QK-1 in C-NeuAc had decreased by only 1.41 log (CFU/ mL) after exposure to simulated acidic gastric fluid. Moreover, the survival rate of the encapsulated and free Pediococcus pentosaceus QK-1 cells were 80.1% and virtually zero, respectively, after passage through the gastrointestinal tract. It was empirically determined that low temperature and freeze-drying were the ideal condition and method to ensure storage longevity of the hydrogel-encapsulated probiotic. Hence, C-NeuAc hydrogel is highly desirable as a food-grade probiotic delivery vehicle.
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高影响因子
CHEMICAL PHYSICS LETTERS
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2022
·
IF 2.719
Xinhe Liu,Yong Kang,Yi Wang
In this work, novel visible-light responsive β-Bi 2 O 3 /Ag 2 WO 4 p-n heterojunction photocatalysts were prepared by a simple in situ deposition method and characterized using XRD, FT-IR, SEM, TEM, XPS, UV–vis and PL. The uniform deposition of Ag 2 WO 4 particles on β-Bi 2 O 3 flakes to form heterojunctions, exhibited excellent photocatalytic activity for the degradation of methylene blue (MB) under visible light in 30 min. Compared with pure β-Bi 2 O 3 and Ag 2 WO 4 samples, the kinetic reaction rate constant of MB degradation by β-Bi 2 O 3 /Ag 2 WO 4 was 48.47 times higher than that of β-Bi 2 O 3 , and the degradation rate was as high as 98.8% with good cycling stability.
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Reaction Chemistry & Engineering
·
2022
·Vol. 7
·期 5
·1191-1198
·
IF 5.2
Linhao Yu,Saravanan Kasipandi,Hong Chen,Yingying Li,Xueli Ma,Zhe Wen,Yongdan Li
Cobalt nanoparticles embedded in graphitic nitrogen-rich carbon nanotubes (Co/GCN) were prepared with a facile method and employed as an efficient catalyst for oxidative esterification of 5-hydroxymethylfurfural (HMF). The introduction of N species to carbon benefits the synergistic effects between the Co nanoparticles and nitrogen-doped carbon nanotube substrate, which modify the surface chemical state of the Co/GCN catalyst and create abundant active sites to improve the HMF conversion. The Co/GCN catalyst carbonized at 800 °C exhibited the best catalytic performance with a 95.8% yield of furan-2,5-dimethylcarboxylate (FDMC) at 98.6% HMF conversion under mild reaction conditions. The effect of acid–base properties of the catalyst on the HMF conversion was investigated and the reaction mechanism of the HMF oxidative esterification was proposed.
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高影响因子
JOURNAL OF CATALYSIS
·
2022
·
IF 8.047
Yi Liu,Ying Chen,Yunli Liu,Zewen Chen,Huan Yang,Zhongxiao Yue,Qing Fang,Yunfei Zhi,Shaoyun Shan
Solar energy is considered as the cleanest, cheapest, and most sustainable energy source, and CO 2 cycloaddition that is drove by solar energy has unique advantages in the aspect of energy and environmental. Therefore, Zn and N co-doped porous carbon nanosheets (ZNCs), which were synthesized by a simple one-step pyrolysis method, as catalysts and photothermal material to photothermally drive cycloaddition of CO 2 . The prepared ZNCs show graphene-like layered structure, uniformly distributed Lewis acid (Zn atoms) sites and Lewis base (N atoms) sites, full spectrum absorption and high photothermal conversion efficiency. More importantly, ZNCs have a higher catalytic efficiency than traditional heating methods because it can be quickly in-situ heated by light, hence the yield of cyclic carbonate reached 91.1% (0.1 MPa CO 2 , 1000 mW·cm −2 full-spectrum irradiation, 12 h). ZNCs were recycled five times without significant reduction in catalytic efficiency, and have high activity to other series of epoxides. A possible CO 2 cycloaddition mechanism which is catalyzed by ZNCs is proposed, including the step of adsorption, ring opening, insertion and cyclic carbonates formation.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2022
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IF 9.136
Shoujun Wang,Dezhi Chen,Zhi-Xia Zhang,Yi Hu,Hongying Quan
Under the global shortage of freshwater resources, capacitive deionization (CDI) has attracted widespread attention as an efficient and energy-saving water purification technology. Herein, N-doped hierarchically porous carbons (NPCs) with micro- meso -macropore, excellent specific capacitance (194.75 F g −1 ), large specific surface area (1903.0 m 2 g −1 ), high mesoporous content, and fast ion transport capability were prepared by the pyrolysis of polyacrylonitrile using nano-silica and ZnCl 2 as pore-making agents. As CDI electrode materials for desalination and heavy metal adsorption, the optimized NPC-0.75 electrode delivered a maximum electrosorption capacity of 19.61 mg g −1 at the optimum operating parameters (1.2 V, 10 mL min −1 , 500 mg L -1 NaCl) and an excellent regeneration performance after continuous electrosorption-desorption cycles. The structure–activity relationship analysis indicated that the mesopore dominates the CDI performance of NPCs in water. In addition, NPC-0.75 electrode showed a high removal capacity for Cu 2+ (36.3 mg g −1 ), Cd 2+ (30.02 mg g −1 ) and Pb 2+ (21.5 mg g −1 ) in water. This study provides new insight into the design of high-efficiency porous carbons toward the CDI from water.
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