Nano Energy
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2019
·
IF 15.548
Sheng Huang,Chao Meng,Min Xiao,Shan Ren,Shuanjin Wang,Dongmei Han,Luyi Sun,Yuezhong Meng
Pseudocapacitive Na + storage based on the fast absorption/desorption kinetics is a new alternative to realize the high rate capability, which rely on increasing the surface area and creating surface vacancies. This means low Na + capacity because of low dielectric constant for the reported pseudocapacitive Na + storage materials. According to the capacitance formula, we find increasing the dielectric constant is a new path to improve the Na + capacity. This dielectricity (other than surface engineering) based pseudocapacitance can be called more real pseudocapacitance. The superparaelectric 2-dimensional (2D) Sn 2 P 2 S 6 has much higher dielectric constant than the bulk counterpart. The identical polaron direction triggered superparaelectricity and high dielectric constant of 2D Sn 2 P 2 S 6 are well verified. And 2D assembly between the 2D Sn 2 P 2 S 6 and graphene construct the compact network for conductivity of electron and Na + . As results, the 2D Sn 2 P 2 S 6 battery based on more real pseudocapacitance delivers alloy-like capacity and long cycle stability.
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CARBOHYDRATE POLYMERS
·
2019
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IF 6.044
Shuangyu Xiong,Luminita Marin,Lian Duan,Xinjian Cheng
Nitroaromatic compounds, especially 2, 4, 6-trinitrophenol, have strong biological toxicity and explosive risks, so the detection of 2, 4, 6-trinitrophenol exhibit importantly practical and scientific significance. In this work, three fluorescence functionalized chitosan CNS 3 , CNS 4 and CNS 5 were prepared using chitosan as matrix. When 2, 4, 6-trinitrophenol (TNP) and/or p-nitrophenol (4-NP) was present in spot, these fluorescent chitosan sensors produced notable fluorescence quenching. It renders the chitosan sensing ability to detect TNP and 4-NP selectively and sensitively. The sensing mechanism is investigated as well. When introduced electron-rich moieties to the fluorescent chitosan, the sensitive detecting ability could be obtained. Excellent recognition ability could reach as low as 0.28 μM. The fluorescence fictionalization cause slight influence to the gel performance of chitosan.
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JOURNAL OF HAZARDOUS MATERIALS
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2018
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IF 6.434
Lan Cao,Changjun Yang,Bingguang Zhang,Kangle Lv,Mei Li,Kejian Deng
ABSTRACT A new ZnO/CoPz(hmdtn) 4 composite as a highly efficient photocatalyst was successfully prepared by cobalt tetra(2-hydroxymethyl-1,4-dithiin)porphyrazine (CoPz(hmdtn) 4 ) impregnated onto the surface of ZnO nanoparticles, the photocatalytic performance of ZnO/CoPz(hmdtn) 4 under both simulated sunlight and visible light (λ ≥ 400 nm) irradiation was assessed by degradation of Rhodamine B (RhB) and phenol in aerated conditions. The ZnO/CoPz(hmdtn) 4 manifested much higher photocatalytic activity than pure ZnO and pure CoPz(hmdtn) 4 , originating from the synergistic effect between CoPz(hmdtn) 4 and ZnO. Furthermore, the XPS analysis revealed that there may be strong interaction between CoPz(hmdtn) 4 and ZnO. Thereby ZnO/CoPz(hmdtn) 4 with excellent stability can maintain high photocatalytic activity over five runs on the basis of the reusability test. The active species generated in the photocatalytic system were verified by electron spin resonance (ESR) technology. A possible mechanism of the synergistic effect between CoPz(hmdtn) 4 and ZnO was also proposed.
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Polymers
·
2018
·Vol. 10
·期 2
·159
·
IF 2.935
Chao Xiong,Shixing Wang,Libo Zhang,Ying Li,Yang Zhou,Jinhui Peng
A new adsorbent(A-PGMA) has been synthesized via functionalizing poly(glycidyl methacrylate) microsphere with 2-aminothiazole and used to adsorb gold ions from aqueous solutions. The adsorbent was characterized by X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET), Zeta potential, scanning electron microscope (SEM) and Fourier transform infrared spectroscopy (FT-IR). The influence factors such as the pH value of the solution, the initial gold ion concentration and the contact time were examined. Simultaneously, the adsorption process of the gold ion on A-PGMA fitted well with the Langmuir and pseudo-second-order models, respectively. The results showed that the maximum adsorption capacity was 440.54 mg/g and the equilibrium time of adsorption was about 3 h under pH 4. Moreover, the adsorbent has a high reusability after five cycles and good selectivity from coexisting ions, including Zn(II), Mg(II), Cu(II), Ge(IV) and B(III). The adsorption mechanisms of gold ions were ion exchange and chelation between the sulfur and nitrogen groups on the surface of A-PGMA and AuCl4−. Therefore, the adsorbent has a great potential for adsorption of gold ions from aqueous solutions.Keywords:adsorption;gold;reusability;mechanism;selectivity
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IET Nanobiotechnology
·
2018
·Vol. 12
·期 7
·946-950
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IF 2.059
Zhuanzhuan Zhang,Xianjun Dai
The conditions were optimised for preparing Alginate oligosaccharide (AOS) nanoliposomes, and Caco-2 cell experiments were carried out to examine their antitumour effects. The optimal formulation of AOS nanoliposomes was as follows: a phosphatidylcholine-to-cholesterol ratio of 5.12, AOS concentration of 8.44 mg/mL, Tween 80 concentration of 1.11%, and organic phase to aqueous phase ratio of 5.25. Under the above conditions, the experimental encapsulation efficiency was 65.84%, and the AOS nanoliposomes exhibited a small particle size of 323 nm. After Caco-2 cells were treated with AOS liposomes and AOS for 24 h, AOS nanoliposomes inhibited the growth of Caco-2 cells to a greater extent than AOS at concentrations of 0.0625, 0.125, 0.25, 0.5 and 1 mg/mL ( P < 0.01). LDH leakage exhibited a concentration-dependent increase following treatment with 0.5-1 mg/mL AOS nanoliposomes, and the inhibitory effect of AOS nanoliposomes exhibited a more significant difference than AOS ( P < 0.01). Cells treated with 0.5 mg/mL and 1 mg/mL AOS nanoliposomes displayed a substantial and significant increase in activity compared with AOS ( P < 0.01). Based on these results, AOS nanoliposomes exerted a more significant effect on inhibiting Caco-2 cell proliferation than AOS.
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CERAMICS INTERNATIONAL
·
2018
·
IF 3.057
Shuyang Li,Jian Liu,Xiaoyong Yang,Yi Ding,Lin Zhu,Bo Liu,Ling Zhang,Shilin Luo,Jiehong Lei,Wenkun Zhu,Tao Duan
Zircon ceramics (ZrSiO 4 ) are promising candidates for actinide immobilization. Here, a series of Zr 1- x Nd x SiO 4- x /2 ( x = 0, 0.02, 0.20, and 1.0) ceramics are prepared to study the effects of phase evolution and acidity on the chemical durability of ZrSiO 4 -based nuclear waste forms. The results show that the chemical stability of the single-phase ZrSiO 4 sample is better than that of the biphasic Zr 0.8 Nd 0.2 SiO 3.9 sample due to the existence of a secondary highly soluble phase (Nd 2 Si 2 O 7 ), which increases the contact area with leachate. The normalized release rates of both zirconium (Zr) and neodymium (Nd) in the Zr 1- x Nd x SiO 4- x /2 ceramic waste forms increase with increasing Nd loading and acid concentration. LR Zr in ZrSiO 4 ceramics and LR Nd in Zr 0.98 Nd 0.02 SiO 3.99 ceramics are the lowest, while LR Zr and LR Nd reach the highest values in the Zr 0.8 Nd 0.2 SiO 3.9 and Nd 2 Si 2 O 7 ceramics, respectively. The normalized release rates of Zr are lower than those of Nd due to the difference in the energies of their bonds with oxygen atoms. Moreover, the changes in the surfaces of the leached ceramics are consistent with their leaching results.
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ACS Sustainable Chemistry & Engineering
·
2018
·
IF 6.14
Yan Xu,Linjie Xie,Di Li,Rong Yang,Deli Jiang,Min Chen
The exploration of earth-abundant and high-efficiency electrocatalysts for water oxidation is of great significance for sustainable energy conversion. Co–Mo-based bimetallic oxides are considered as promising candidates for the oxygen evolution reaction (OER) due to their high intrinsic activity and low cost. In this work, we reported an interfacial engineering design of CoMoO4 nanoplate arrays wrapped with Ni(OH)2 nanosheets supported on Ni foam for high-performance OER. Remarkably, benefiting from the hierarchical heterostructure arrays with strong interfacial interaction, enlarged surface areas, and more active sites, the optimized CoMoO4-Ni(OH)2 electrocatalyst manifests the excellent OER catalytic performance with a low overpotential of 349 mV at the current density of 100 mA cm–2, a long-term stability, and high (nearly 100%) Faradaic efficiency, which is superior to those of most previously reported Co–Mo-based bimetallic oxides electrocatalysts. Therefore, this interfacial engineering demonstrates an effective strategy for designing and fabricating high-performance electrocatalysts for OER reaction.
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
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2018
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IF 2.891
Zhi Zhu,Wenqian Fan,Zhi Liu,Yang Yu,Hongjun Dong,Pengwei Huo,Yongsheng Yan
The present study describes a metal-free biochar-based photocatalyst of g-C 3 N 4 -C, in presence of an abundant fade magnolia as carbon precursor via facial in-situ together growth method. As a consequence, the g-C 3 N 4 -C shows a better degradation efficiency to 2-Mercaptobenzothiazole (90%) than pure g-C 3 N 4 (49%) under the visible light. The improved photocatalytic performance of g-C 3 N 4 is attributed to the biochar can significantly against the g-C 3 N 4 reunion and stacking during high temperature treatment, because the biochar can act as the attachments that make the g-C 3 N 4 flat and no accumulation, which will further increase the active sites. Additionally, photo-electrochemical measurements proved the separation efficiency of electron-holes of g-C 3 N 4 is enhanced by introduced of biochar, due to its good electron transmission ability. Moreover, the ESR measurement and capture experiment further confirmed the active radicals on degradation of MBT are h + and O 2 − . This work may provide a promising approach for wastewater treatment by waste utilization of solid biomass and increasing the photocatalytic performance of g-C 3 N 4 .
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CHINESE JOURNAL OF POLYMER SCIENCE
·
2018
·Vol. 36
·期 5
·612-619
·
IF 2.016
Wang Ye,Hu Ting-Ting,Han Xiao-Long,Wang Yu-Qi,Li Ji-Ding
Cu(OH) 2 nanowires were prepared and incorporated into poly(vinylidene fluoride) (PVDF) to fabricate Cu(OH) 2 -PVDF ultrafiltration (UF) membrane via immersion precipitation phase inversion process. The effect of Cu(OH) 2 nanowires on the morphology of membranes was investigated by X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM), scanning electron microscopy (SEM) and X-ray diffraction (XRD) measurements. The results showed that all the Cu(OH) 2 -PVDF membranes had wider fingerlike pore structure and better hydrophilicity, smoother surface than pristine PVDF membrane due to the incorporation of Cu(OH) 2 nanowires. In addition, water flux and bovine serum albumin (BSA) rejection were also measured to investigate the filtration performance of membranes. The results indicated that all the Cu(OH) 2 -PVDF membranes had high water flux, outstanding BSA rejection and excellent antifouling properties. It is worth mentioning that the optimized performance could be obtained when the Cu(OH) 2 nanowires content reached 1.2 wt%. Furthermore, the membrane with 1.2 wt% Cu(OH) 2 nanowires showed outstanding oil-water emulsion separation capability.
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JOURNAL OF HAZARDOUS MATERIALS
·
2018
·
IF 6.434
Kaiyu Jiang,Caihuan Huang,Rui Jiao,Weibin Bai,Jie Zheng,Shiyi Ou
Acrolein (ACR), glyoxal (GO), methylglyoxal (MGO), hydroxymethylfurfural (HMF), and malondialdehyde (MDA) are toxic contaminants for humans. This work aimed to investigate whether intake of proteins can mitigate their toxicity. Simulated gastrointestinal digestion of proteins from pork, chicken, milk powder and soy protein isolate eliminated amount of ACR, GO, MGO, HMF, and MDA. Among six amino acids, cysteine showed highest capacity for elimination of these toxic compounds through the formation of adducts; it reached the highest elimination capacity for GO, MGO, ACR, MDA, and HMF in 40 min at pH 2.0, and 20 min at pH 7.0. The formed adducts between cysteine and GO, MGO, or ACR showed much lower toxicity against Caco-2 cells. Incubation of the cells with 8 mM GO and MGO for 48 h decreased the cell viability to 16.1%, 16.9% respectively; while incubation of the same concentration of their adducts still kept the cell viability at 82.2% and 81.6% respectively. Cysteine showed much higher detoxifying capacity for ACR than GO and MGO, which can lower the toxicity of ACR toward Caco-2 cells by 80 times.
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PHYSICAL CHEMISTRY CHEMICAL PHYSICS
·
2018
·Vol. 20
·期 38
·24796-24806
·
IF 3.906
Chensheng Ma,Chris Tsz-Leung Chan,Ruth Chau-Ting Chan,Allen Ka-Wa Wong,Bowie Po-Yee Chung,Wai-Ming Kwok
Apart from being an analogue of the prototype for photoinduced intramolecular charge transfer (ICT), 2-ethylhexyl 4-dimethylaminobenzoate (EHDMABA) is also one of the earliest patented and most commonly used sunscreen components. There is, however, little documented information about the photophysics and factors affecting the photophysics of this molecule. Such information is of importance for both the understanding of the ICT reaction and assessing the underlying process of photoprotection, especially in view of the “sunscreen controversy” that has arisen from the contrasting in vivo vs. in vitro photobiological results on this and related UV filters. We report herein a femtosecond broadband time-resolved fluorescence (fs-TRF), complemented by transient absorption (fs-TA) to allow a full probe of the excited state cascades for EHDMABA and two of its derivatives in solvents of varied properties. The results provide direct evidence for a nearly solvent independent inner sphere ICT reaction occurring on the sub-picosecond time scale, and an ensuing solvent dictated deactivation of the ICT state. The ICT state in the aprotic solvent acetonitrile decayed solely through the intrinsic intersystem crossing (ISC) to produce a potentially harmful triplet excited state. In the protic solvent, the solvation and formation of ICT-induced solute–solvent hydrogen (H)-bonding opened the originally inaccessible internal conversion (IC) channel of the ICT state, leading to the rapid reformation of the ground state molecule with a unitary efficiency in the aqueous solution. This H-bonding-mediated IC restrained or eliminated the intrinsic ISC, providing a mechanism at the molecular level for the benign dissipation of the electronic excitation. The precise rate of IC was observed to vary with the alkoxy substituent and its efficiency was affected by the H-bonding capacity of the solvent. The findings of this work demonstrate the pivotal role of the microenvironment and the direct participation of solvent molecules through H-bonding in drastically altering the nonradiative dynamics and promoting or inhibiting photostability and photoprotection. This may assist in developing next-generation UV filters and help in improving formulation design for the optimal efficacy of sunscreen products. The pronounced H-bonding-induced fluorescence quenching and variation in the fluorescence wavelength imply that these molecules may also serve as a sensitive fluorescence probe for the H-bonding properties of the microenvironment.
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ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY
·
2018
·
IF 3.974
Linbao Zhang,Ying Hu,Wei Sun,Si Chen,Xiaoping Jia,Wengui Cai
Di-(2-ethylhexyl) phthalate (DEHP) is currently the most frequently detected phthalic acid esters (PAEs) compounds and can induce diverse toxicities on aquatic organisms. To understand the molecular responses of fish to DEHP, we performed transcriptomic profiles in liver of tilapia ( Oreochromis niloticus ) which were exposed to environmental concentration of DEHP. A total of 30.10 Mb and 30.16 Mb clean reads were retrieved from the control and DEHP treated libraries, respectively. De-novo assembly of all the clean reads obtained 58,585 unigenes. After comparing the two libraries, 2814 and 1790 genes were identified as significantly increased and depressed, respectively. Gene ontology (GO) classification system and Kyoto Encyclopedia of Genes and Genomes (KEGG) database analysis demonstrated that DEHP significantly disturbed the expression level of genes associated with immunity, endocrine and reproductive system, lipid metabolism and so on. Quantitative real-time PCR was performed to validate the results of RNA-sequencing (RNA-seq) analysis. The resulting data provide new insights for exploring the molecular basis of tilapia response to DEHP exposure.
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