JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2015
·
IF 3.368
Chunyan Sun,Feng Zhang,Jianfang Cao
The faujasite-Y confined ammonium molybdophosphate (AMP–Y) were successfully synthesized for the first time using ammonium molybdophosphate and natural clay from Qaidam Basin as starting materials. The final products were characterized by XRF, XRD, FTIR, 27 Al and 31 P MAS NMR, and N 2 adsorption/desorption, which indicated that Qaidam natural clay is a promising low-cost precursor for the production of zeolite Y support. Various loadings of ammonium molybdophosphate could be well encapsulated in the supercage of Y zeolite using a ‘build-bottle-around-ship’ method. The resultant composite materials were effective for the adsorption of cesium ion from solution.
研究领域:
材料科学
·
环境科学
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DOI
PubMed
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2024
·
IF 4.8
Xiaoqian Li,Shenyong Ren,Lu Liu,Chi Yang
A core-shell structured USY-xTT@NiMo catalyst was prepared through thermal treatment method and evaluated for the catalytic hydrodesulfurization (HDS) performance toward dibenzothiophene (DBT). The shell assembled from NiMoS nano-wool provided abundant active site. This nano-wool morphology and core-shell structure resulted in the catalyst with enhanced specific surface area, pore volume, lower interaction between the support and active metals, and facilitated metal dispersion. In addition, the nano-wool morphology and core-shell structure also promoted the degree of sulfurization and provided more sulfur vacancies, which enhanced the HDS performance of the corresponding catalysts. An efficient USY-16TT@NiMo catalyst with shorter slab lengths (average 2.50 nm), higher average stacking number (3.37 layers), and more edge active sites was assembled, which showed superior k HDS value of DBT up to 8.29 × 10 −4 mol g −1 h −1 and high direct desulfurization selectivity to be 88 %.
研究领域:
催化化学
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材料科学
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产品关联
DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2018
·
IF 2.746
Lili Yu,Hui Xu,Hou Chen,Shengxiao Zhang,Tingting Jiang,Liangjiu Bai,Wenxiang Wang,Shanmin Gao,Juan Jin
A label-free DNA Y junction sensor for amplified detection of Hg 2+ has been demonstrated by using thymine-Hg 2+ -thymine (T-Hg 2+ -T) recognition, cascade toehold-mediated DNA strand displacement and dye staining double-stranded DNA (dsDNA). In our work, assistant DNA could bind with the first hairpin DNA with toehold domains by the help of thymine-Hg 2+ -thymine (T–Hg 2+ –T) base pairs recognition. The second hairpin DNA with toehold domains will then hybridize with the complementary sequences in first hairpin DNA, which again initiates a new toehold domains to open the third hairpin DNA, triggering a cascade strand displacement reaction. Exonuclease III (Exo III) was added to digest the three hairpin DNA with recessed 3′ ends in the absence of Hg 2+ to reduce the background signal. As a comparison, Exo III is replaced by GO to reduce the background signal because single-strand DNA (ssDNA), three hairpin DNAs with intercalated dye could be adsorbed onto the surface of GO and lead to quenched fluorescence. The method, designed in a simple “mix, incubate, and detect” format, can detect concentrations of Hg 2+ as low as 0.031 nM, and exhibit good selectivity and practical application.
研究领域:
生物化学
·
环境科学
·
分析化学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
·
2025
·
IF 4.7
Hezheng Sun,Guoqing Liu,Yi Zhao,Jingcun Shao,Changhui Xin,Yanting Tang,Xin Yu
Bisphenol A is an environmental hormone that shows a significant impact on human health. The removal of bisphenol A substances from the surrounding environment is of great significance for the humanity sustainable development. Current work focuses on synthesizing self-doped Nb 3 O 7 (OH) nanostructure and eosin Y/Nb 3 O 7 (OH) composites with high surface areas through a solvothermal process for bisphenol A degradation under visible-light illumination. The prepared Nb 3 O 7 (OH) sample demonstrated a noticeable photocatalytic performance toward bisphenol A degradation. Notably, the obtained eosin Y/Nb 3 O 7 (OH)-1.0 % composite not only exhibited efficient visible-light harvesting and high surface area but also showed significantly improved charge separation and bisphenol A degradation compared to pristine Nb 3 O 7 (OH) sample. The rate constant of the eosin Y/Nb 3 O 7 (OH)-1.0 % sample for bisphenol A degradation was approximately 0.04252 min −1 , which was 7.85 times that of pristine Nb 3 O 7 (OH) sample. Furthermore, the eosin Y/Nb 3 O 7 (OH)-1.0 % composite achieved approximately 59.76 % mineralization of bisphenol A within 20 min and 75.28 % mineralization within 40 min under visible-light illumination. Additionally, the effects of experimental parameters on bisphenol A degradation and the dye-sensitization mechanism were proposed. The current work suggests the obvious advantages of defective Nb 3 O 7 (OH) nanostructure in fabricating high-performance composite photocatalysts for eliminating emerging pollutants.
研究领域:
环境科学
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纳米技术
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材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
ACS Sustainable Chemistry & Engineering
·
2023
·
IF 8.4
Siyu Pan,Jun Yan,Xu Peng,Zhou Xu,Qi Zeng,Zhonghui Wang,Minzhong Zhao,Yi Chen
In the poly(vinyl chloride) (PVC) industry, waste cooking oil (WCO)-derived epoxidized fatty acid methyl esters (EFAMEs) represent a promising bio-alternative to conventional ortho-phthalate plasticizers that are being phased out due to their toxicity and nonrenewable nature. However, to improve the leaching resistance of EFAMEs, the WCO feedstock has to go through multistage distillation at particularly high temperatures under vacuum conditions for saturated component removal, resulting in intensive energy consumption, a significant waste of the feedstock, and a final bioplasticizer with a still faster leaching rate than those of ortho-phthalates. Here, we report a strategy that can Y-shape all components in WCO-derived EFAMEs with another short, polar ester chain via a nucleophilic substitution reaction of the feedstock mixture with dimethyl carbonate. This strategy entails no utilization of an energy-intensive procedure and, importantly, converts all components in the WCO feedstock into the final bioplasticizer. Relative to ordinary EFAMEs, the Y-shaped epoxidized fatty acid methyl diester exhibits a significantly suppressed leaching rate. Under certain scenarios, it even leaches at a rate equivalent to or slower than that of di-(2-ethylhexyl) phthalate (DEHP), the most ubiquitously applied member of the ortho-phthalate family. With this strategy in hand, the renewable WCO may be converted into a high-performance bioplasticizer in an energy-efficient and atom-economic manner to support the phase-out of ortho-phthalates in the PVC industry.
研究领域:
材料科学
·
化学工程
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
CORROSION SCIENCE
·
2022
·
IF 7.72
Yanan Cui,Zhice Yang,Tao Zhang,Fuhui Wang
The inhibition mechanism of four inhibitors with different charge on Mg-Gd-Y alloy was investigated experimentally and theoretically. The different charge of inhibitor evoked the preferential adsorption behavior, changing the susceptibility of Mg-Gd-Y alloy to micro-galvanic corrosion. Moreover, the adsorption of inhibitor changed the surface energy of embryos of corrosion product, and strongly suppressed the nucleation rate of corrosion product, leading to poor protective performance. Thus, the inhibitor with anion, exhibiting satisfactory inhibition efficiency for AZ/AM series alloys, showed worse inhibition for the Mg-Gd-Y alloy. Finally, the strategy to select and/or synthesize inhibitors for Mg-RE alloys was presented.
研究领域:
材料科学
·
腐蚀与防护
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DOI
高影响因子
Journal of Physical Chemistry C
·
2018
·
IF 4.484
Zhiqiang Xie,Congbiao Chen,Bo Hou,Dekui Sun,Heqin Guo,Jungang Wang,Debao Li,Litao Jia
The nature of high-silica H–Y acid sites in dimethoxymethane carbonylation is investigated by NH3 poisoning with a combination of reaction results, diffuse reflection infrared Fourier transform spectra, and NH3 temperature-programmed desorption. After NH3 poisoning of H–Y, ammonia desorption of zeolites NH4–Y was conducted at different temperatures to obtain catalysts HNH4–Y that gradually exposed different acid sites. The zeolites thus produced catalyzed dimethoxymethane carbonylation with a linear dependence of the conversion on the ammonia desorption temperature before the plateau stage. It was observed that strong Brønsted acids in zeolite Y catalyzed the reaction more selectively toward the main product methyl methoxyacetate, and weak Brønsted acids catalyzed the reaction more selectively toward the byproduct methyl formate. Furthermore, the turnover frequency of Brønsted acids varied significantly among the Brønsted acids and decreased with acid strength. This finding suggested that only 10.1–18.3% of the total Al in zeolite Y with Si/Al ratios of 15, 30, and 40 contributed to the total framework Brønsted acids.
研究领域:
化学工程
·
催化科学
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产品关联
DOI
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2022
·
IF 9.221
Qi Wang,Wenyong Li,Juan Xia,Hai Wu,Lijun Wu,Jianguo Xu
The construction of DNA nanodevices is vital for disease diagnosis and biomedical study. Herein, we proposed a ternary DNA nanomachine for microRNA determination using a molecular beacon (MB) coupled Y shape probe (MB-YP). The MB-YP was a tripartite junction scaffold connected with MB-Y I , Y II , and Y III . The target miRNA firstly recognizes MB-Y I , activating the MB-Y I -DNA nanomachine to produce endogenous primer I (EP I ) responsible for the activation of Y II -DNA nanomachine. The Y II -DNA nanomachine then allows the production of numerous EP II , which in turn activates the Y III -DNA nanomachine to produce EP III for re-activating MB-Y I -DNA nanomachine. The stepwise operated MB-Y I -DNA nanomachine, Y II -DNA nanomachine, and Y III -DNA nanomachine constituted the ternary DNA nanomachine and the repeated use of EP I , EP II , and EP III permits it an all-in amplification. These features lead to the opening of MB-Y I for emitting strong fluorescence. As low as 1 fM miRNA can thus be quantitatively detected and the linear response of the miRNA is from 1 fM to 100 pM (six orders of magnitude). Moreover, the nanomachine is specific to distinguish target miRNA from one-base mutant, inserted, and deleted target analogs. Its practicability was demonstrated by confirming miRNA-21 is overexpressed in clinical human serums from lung cancer patients than healthy donors.
研究领域:
生物医学工程
·
分子生物学
·
纳米技术
·
癌症诊断
✓ 已验证
产品关联
DOI
高影响因子
ANALYTICA CHIMICA ACTA
·
2014
·
IF 4.517
Xia Hao,Jing Lei Lei,Nian Bing Li,Hong Qun Luo
A simple and effective method for the detection of electrochemically inactive sodium dodecyl sulfate (SDS) has been designed, based on different binding affinity of polyethyleneimine (PEI) toward electrochemically active eosin Y and electrochemically inactive SDS. The stronger binding affinity of the PEI toward SDS than eosin Y results in the decrease of the redox peak current of surface confined eosin Y and provides a quantitative readout for the SDS. The difference in value of the cathodic peak current showed a linear relationship with SDS concentration in a concentration range from 1 to 40 μg mL −1 , and a detection limit of 0.9 μg mL −1 for SDS was obtained. Furthermore, the method has been successfully applied to the detection of SDS in real samples. The developed approach provided a simple and reliable detection for SDS and might have potential applications in electrochemical methods for inactive molecules.
研究领域:
分析化学
·
电化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY
·
2021
·Vol. 37
·期 12
·1-12
·
IF 3.312
Zhao Zhenzhen,Liu Chao,Xu Qianqian,Ahmad Shahbaz,Zhang Haiyang,Pang Yu,Aikemu Abudumukeyiti,Liu Yang,Yan Hai
A promising bacterial strain for biodegrading dibutyl phthalate (DBP) was successfully isolated from activated sludge and characterized as a potential novel Microbacterium sp. USTB-Y based on 16S rRNA sequence analysis and whole genome average nucleotide identity (ANI). Initial DBP of 50 mg/L could be completely biodegraded by USTB-Y both in mineral salt medium and in DBP artificially contaminated soil within 12 h at the optimal culture conditions of pH 7.5 and 30 ℃, which indicates that USTB-Y has a strong ability in DBP biodegradation. Phthalic acid (PA) was identified as the end-product of DBP biodegraded by USTB-Y using GC/MS. The draft genome of USTB-Y was sequenced by Illumina NovaSeq and 29 and 188 genes encoding for putative esterase/carboxylesterase and hydrolase/alpha/beta hydrolase were annotated based on NR (non redundant protein sequence database) analysis, respectively. Gene3781 and gene3780 from strain USTB-Y showed 100% identity with dpeH and mpeH from Microbacterium sp. PAE-1. But no phthalate catabolic gene ( pht ) cluster was found in the genome of strain USTB-Y. The results in the present study are valuable for obtaining a more holistic understanding on diverse genetic mechanisms of PAEs biodegrading Microbacterium sp. strains.
研究领域:
环境微生物学
·
基因组学
✓ 已验证
DOI
PubMed
高影响因子
JOURNAL OF NUCLEAR MATERIALS
·
2017
·
IF 2.048
Yi Ding,Xinggui Long,Shuming Peng,Dong Zhang,Zhaoyi Tan,Xirui Lu
Zr 1− x − y Ce x Nd y O 2− y/ 2 ceramics, which were designed as waste form materials, were obtained by simultaneous substitution of Ce 4+ and Nd 3+ for Zr 4+ in ZrO 2 . The influences of the simultaneous substitution of Ce and Nd on phase transformation of ZrO 2 were investigated systematically. Also, the aqueous durability of the ceramics was evaluated. The results show that the phase transformation caused by the simultaneous substitution mainly relates to the total content of Ce and Nd. The ZrO 2 ceramics containing Ce + Nd < 30 mol% exhibit both monoclinic and cubic phases, while the ceramics containing Ce + Nd ≥ 30 mol% are cubic phase. And the cubic phase can be stabilized by incorporating 30 mol% Ce + Nd. Moreover, LR i are modified by the incorporation of Ce and Nd, because of the presence of oxygen vacancies . The Nd and Ce co-doped zirconia waste form exhibit excellent aqueous durability (∼10 −5 g m −2 d −1 ).
研究领域:
材料科学
·
核废料管理
·
陶瓷工程
✓ 已验证
产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2018
·
IF 3.927
Yijie Han,Cheng Chen,Yuxin Li,Lixiang Zhou,Yeqing Lan,Ying Li
Cu-Y binary oxysulfide was synthesized for the first time. A series of batch experiments were conducted to determine the optimum conditions for preparing the adsorbent and further investigate the effects of the initial pH and coexisting anions on the removal of arsenic. The results indicate that the adsorbent displays an extremely excellent performance in removing both As(III) and As(V). The maximal adsorption capacities at the initial pH 6.0 are 263.16 and 270.27 mg/g for As(III) and As(V), respectively. The adsorbent remains relatively stable even at the initial pH 3 and at this pH it also exhibits a very high removal efficiency for As(V). Based on Fourier-transform infrared (FTIR) spectrometer and X-ray photoelectron spectrometer (XPS) analyses and other results obtained in our experiments, a possible mechanism for the removal of arsenic is proposed. The dissolved O 2 is activated to O 2 − via a single-electron transfer reaction from Cu(I) on the adsorbent, which oxidizes As(III) to As(V). Then, arsenate anions are adsorbed onto the surface of the adsorbent and the adsorbed arsenate anions further react with the hydroxyl groups on the surface of the adsorbent via an ion exchange or precipitate with Y(III) on the surface of the adsorbent .
研究领域:
环境科学
·
化学
·
水处理
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）