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1.
ACS Appl Mater Interfaces ; 14(33): 37771-37781, 2022 Aug 24.
Article in English | MEDLINE | ID: mdl-35960183

ABSTRACT

Active metal ions often show a strong cutting effect on the chemical bonds during high-temperature thermal processes. Herein, a one-pot metal ion cutting-assisted method was adopted to design defect-rich MoS2-x nanosheet (NS)/ZnS nanoparticle (NP) heterojunction composites on carbon nanofiber skeletons (CNF@MoS2-x/ZnS) via a simple Ar-ambience annealing. Results show that Zn2+ ions capture S2- ions from MoS2 and form into ZnS NPs, and the MoS2 NSs lose S2- ions and become MoS2-x ones. As sulfur hosts for lithium-sulfur batteries (LSBs), the CNF@MoS2-x/ZnS-S cathodes deliver a high reversible capacity of 1233 mA h g-1 at 0.1 C and keep 944 mA h g-1 at 3 C. Moreover, the cathodes also show an extremely low decay rate of 0.012% for 900 cycles at 2 C. Series of analysis indicate that the MoS2-x NSs significantly improve the chemisorption and catalyze the kinetic process of redox reactions of lithium polysulfides, and the heterojunctions between MoS2-x NSs and ZnS NPs further accelerate the transport of electrons and the diffusion of Li+ ions. Besides, the CNF@MoS2-x/ZnS-S LSBs also show an ultralow self-discharge rate of 1.1% in voltage. This research would give some new insights for the design of defect-rich electrode materials for high-performance energy storage devices.

2.
Huan Jing Ke Xue ; 39(7): 3409-3417, 2018 Jul 08.
Article in Chinese | MEDLINE | ID: mdl-29962168

ABSTRACT

Using selected sepiolite (SEP) and biochar (BC) as contrasts, we investigated the effects of a new cross-linked modified chitin (CC) on the bioavailability of Pb and Cd in soils, the yield of rice, and the absorption and accumulation of Pb and Cd in different parts of rice plants in a field environment. We hope this study provides the basis for the application of this material to improve soil fertility, and a direction for further soil improvement studies. A field experiment was carried out in 2015-2016 on selected Pb- and Cd-contaminated rice fields in Linghai, Liaoning. The changes in soil pH and available Pb and Cd in the soil were analyzed after the rice was harvested(October 2016). The effects of different treatments on the growth traits and yield of rice, the absorption of Pb and Cd by rice roots, stems and leaves, and grains were compared. The results showed that adding 167-333 kg·hm-2 CC could increase the soil pH value by 0.36-0.45 units, decreasing the contents of available Pb and Cd in the soil by 46.39%-64.01% and 29.73%-43.24% respectively (P<0.05). This treatment significantly reduced the Pb and Cd contents in all parts of rice (P<0.05) compared to conventional fertilization; Pb and Cd contents in different parts of rice were significantly reduced (P<0.05) by 16.09%-38.14% and 21.22%-31.38% in the root, 19.17%-46.92% and 25.66%-45.34% in the stem and leaf, and 29.47%-58.25% and 44.75%-64.02% in the grain, respectively. The treatment of adding 333 kg·hm-2 CC (CC-2) reduced the contents of Pb and Cd in rice grains to 0.2041±0.011 mg·kg-1 and 0.1922±0.021 mg·kg-1, respectively, which were lower than or close to the limit values of Pb and Cd in rice (0.20 mg·kg-1) as per GB 2762-2005. Compared to conventional fertilization, SEP treatment, and BC treatment, without adding any amendments, the yield per mu of rice under CC treatment increased by 33.6-47, 27.6-44, and 8.67-34.77 kg, respectively. The effect of CC-2 treatment on yield was the most obvious; the yield of rice per mu increased by 47 kg, and the yield increase rate was 8.59%. The ability of CC to repair soil contaminated by Pb and Cd and to reduce the contents of Pb and Cd in rice was not weaker than that of SEP and BC. The CC treatment also controlled the migration and redistribution of Pb and Cd in soil-rice systems, and significantly increased the yield of rice. It has good potential to ensure the safe production of rice.


Subject(s)
Cadmium/metabolism , Chitin/chemistry , Lead/metabolism , Oryza/metabolism , Soil Pollutants/metabolism , Soil/chemistry , Farms , Fertilizers
3.
Cell Biochem Biophys ; 62(3): 409-14, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22081437

ABSTRACT

The objective of this study was to analyze the influence of TNF-α on rat mesenchymal stem cells (MSCs) and to assess feasibility of MSC transplantation to repair ischemic injury. In this study, adhesion molecules and cell specific surface markers on MSCs were measured after exposure to different concentrations of TNF-α. MSCs stimulated with varying concentrations of TNF-α were cultured with aortic endothelial cells, and the adhesion rate was measured. MSCs were then stimulated with an optimum concentration of TNF-α as determined in vitro, and injected intravenously into rats with ischemic hind limb injury. The number of MSCs in muscle samples from the ischemic area was counted. The results showed that (1) TNF-α induced a concentration-dependent increase in VCAM-1 expression in MSCs, whereas the expression of L-selectin, ICAM-1 and VLA-4 did not change significantly. Expression of MSC-specific antigens was unchanged. (2) MSCs pretreated with 10 ng/ml TNF-α showed significantly increased adhesion to endothelial cells in vitro, and accumulated to a greater extent in the areas of ischemic damage in rat hind limbs. We were able to conclude that TNF-α has no effect on expression of MSC-specific markers, but can increase the expression of VCAM-1 on rat MSCs. Suitable concentrations of TNF-α can promote MSC adhesion to endothelial cells and migration to damaged tissue.


Subject(s)
Cell Movement/drug effects , Ischemia/therapy , Mesenchymal Stem Cells/drug effects , Tumor Necrosis Factor-alpha/pharmacology , Animals , Cell Adhesion/drug effects , Disease Models, Animal , Endothelial Cells/cytology , Endothelial Cells/metabolism , Integrin alpha4beta1/metabolism , Intercellular Adhesion Molecule-1/metabolism , L-Selectin/metabolism , Mesenchymal Stem Cell Transplantation , Mesenchymal Stem Cells/cytology , Mesenchymal Stem Cells/metabolism , Rats , Rats, Wistar , Vascular Cell Adhesion Molecule-1/metabolism
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