SENSORS AND ACTUATORS B-CHEMICAL
·
2015
·
IF 4.097
Shaofei Zhang,Hui Yang,Ying Ma,Yu Fang
A bis-nitrobenzoxadiazole (NBD) derivative of calix[4]arene (L 1 ) and a control compound (L 2 ), mono-NBD derivative of the calixarene were designed and prepared via click chemistry. Fluorescence studies demonstrated that L 1 as created can function as a switch with the presence of Ag + in THF, of which the free state of L 1 emits at ∼527 nm, but the binding state at 576 nm. Based upon this discovery, L 1 was studied as a chemo-sensor of Ag + in a mixture solvent of THF and H 2 O with a detection limit (DL) of ∼6.2 × 10 −7 mol/L. Presence of other commonly found metal ions shows little effect upon the determination. Moreover, the L 1 in the Ag + -L 1 complex could be fully released with introduction of HCHO, a bases for the sensitive and selective detection of the toxic chemical. The DL of this test is 6.6 × 10 −7 mol/L. Interestingly, binding and releasing of the fluorescent ligand could be repeated for at least 5 times. Furthermore, both sensing could be performed in a visualized manner. It is believed that the fluorescent compound as created should have a potential to find real-life applications.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2017
·
IF 3.133
Qiqi Nie,Yongbo Wang,Licong Jia,Bei Liu,Enzhou Liu,Xiaoyun Hu,Jun Fan
In this paper, a novel detection method based on luminescence resonance energy transfer (LRET) system for sensitive detection of Mn 2+ ions has been proposed. The positively charged upconversion nanoparticles capped with polyethyleneimin (PEI-UCNPs) and negatively charged Ag NPs capped with tripolyphosphate (P 3 O 10 5− -Ag NPs) were bound through electrostatic interaction . They were used as energy donors and acceptors, respectively. The green upconversion luminescence could be quenched because of a good overlap between the UCNPs emission and the Ag NPs absorption spectra . Nevertheless, the LRET was disrupted and the green upconversion luminescence was restored in the presence of Mn 2+ because of the coagulation of P 3 O 10 5− -Ag NPs. Thus, the relative luminescence intensity increased as the concentrations of Mn 2+ increased. The response is linear to the concentrations of Mn 2+ in the range from 0.2 to 5 μM, and the detection limit is evaluated to be 150 nM (S/N = 3). This probe was easy to operate with satisfactory selectivity and excellent sensitivity, which would be able to satisfy the requirements of Mn 2+ -related detection.
✓ 已验证
产品关联
DOI
高影响因子
ENVIRONMENTAL POLLUTION
·
2017
·
IF 5.099
Yongguang Yin,Dan Han,Chao Tai,Zhiqiang Tan,Xiaoxia Zhou,Sujuan Yu,Jingfu Liu,Guibin Jiang
Photo-reduction of Ag + to silver nanoparticle (AgNPs) by dissolved organic matter (DOM) is a possible source of naturally occurring AgNPs. However, how this photo-reduction process is influenced by ubiquitous metal ions is still not well understood. In addition, in previous studies, the formation of AgNPs in DOM solution was usually monitored by UV-Vis spectroscopy, and there is still lack of quantitative analysis for the formed AgNPs. In the present study, the role of Fe 2+ /Fe 3+ at environmental concentration level on this photochemical process was investigated, and the enhanced formation of AgNPs by Fe 2+ /Fe 3+ was probed and quantified by using UV-Vis spectroscopy, transmission electron microscopy , and liquid chromatography-inductively coupled plasma mass spectrometry. It was demonstrated that while Fe 3+ can oxidize AgNPs to release Ag + , Fe 2+ can reduce Ag + into AgNPs. However, the DOM-induced reduction of Fe 3+ makes iron an effective electron shuttle between DOM and Ag + , and both Fe 2+ and Fe 3+ enhanced AgNP formation. The impacts of environmentally relevant factors, including DOM concentration and solution pH, on this process were studied comprehensively, which showed that the catalytic role of iron was more significant at higher DOM concentration and lower pH. This iron-enhanced formation of AgNPs in photo-irradiated Ag + -DOM solution have great environmental implications on the formation of natural AgNPs and the transformation of engineered AgNPs in acidic surface water with high iron content.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2017
·
IF 9.446
Chenxi Zhang,Kai Yu,Yajun Feng,Yue Chang,Ting Yang,Ying Xuan,Da Lei,Lan-Lan Lou,Shuangxi Liu
The novel visible-light-driven 3DOM-SrTiO 3 /Ag/Ag 3 PO 4 ternary composites were fabricated and used as photocatalysts in the degradation of organic contaminants, including RhB, phenol , and MB. Through the XRD, SEM, TEM, DR UV–vis, XPS, PL spectroscopy, N 2 sorption , and photoelectrochemical measurement, the obtained 3DOM-SrTiO 3 /Ag/Ag 3 PO 4 ternary composites were well characterized. The effects of SrTiO 3 :Ag 3 PO 4 molar ratio and stop-bands of 3DOM-SrTiO 3 on the catalytic performance were systemically investigated. 3DOM-SrTiO 3 /Ag/Ag 3 PO 4 ternary composite photocatalysts exhibited notably enhanced activity compared with single 3DOM-SrTiO 3 and Ag 3 PO 4 catalyst. Among these ternary photocatalysts, S35A65(300) exhibited the most excellent photocatalytic performance under visible light irradiation, which could be mainly attributed to synergy effect of the notably improved separate efficiency of photogenerated electron-hole pairs and the suitable stop-bands of 3DOM-SrTiO 3 (300) material. Although the gradually reduced activity in cycling tests was obtained over S35A65(300) under visible light irradiation, an excellent durability could be achieved for S35A65(300) under UV–vis light irradiation. No obvious loss in photocatalytic efficiency was observed after six cycles for RhB degradation. The notably improved enhanced durability of 3DOM-SrTiO 3 /Ag/Ag 3 PO 4 ternary composites under UV–vis light irradiation could be mainly attributed to the Z-scheme mechanism of this ternary composite photocatalyst.
✓ 已验证
产品关联
DOI
高影响因子
BIORESOURCE TECHNOLOGY
·
2017
·
IF 5.651
Zheng-Zhe Zhang,Jia-Jia Xu,Zhi-Jian Shi,Ya-Fei Cheng,Zheng-Quan Ji,Rui Deng,Ren-Cun Jin
The increasing application of engineered nanoparticles (NPs) has posed an emerging challenge to wastewater treatment processes. The short-term impacts of CuNPs, CuONPs, ZnONPs and AgNPs on anaerobic ammonium oxidation (anammox) process were investigated firstly in this study. CuONPs, ZnONPs and AgNPs up to 50 mg g −1 suspended solid (SS) did not affect anammox activity, reactive oxygen species (ROS) production or cell membrane integrity. However, 1.25 mg g −1 SS CuNPs significantly inhibited the anammox activity and the loads that caused 50% inhibition were 4.64 ± 1.24 and 3.27 ± 0.79 mg g −1 SS for anammox granules and flocs, respectively. 5 mg g −1 SS CuNPs caused serious accumulation of the toxic intermediate N 2 H 4 . Furthermore, CuNPs interacted with extracellular polymeric substances by specifically bonding to tyrosine or tryptophan-containing groups, C-O-C in polysaccharides and –OH in polymeric compounds. Therefore, this study calls for more attention to the risks of NPs to the anammox-based processes.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
INORGANIC CHEMISTRY
·
2017
·
IF 4.857
Yu-Hang Fan,Hui-Yi Zeng,Xiao-Ming Jiang,Ming-Jian Zhang,Bin-Wen Liu,Guo-Cong Guo,Jin-Shun Huang
Quaternary metal thiophosphates containing second-order Jahn–Teller distorted d10 Ag+ and lone-pair cations, Ag3Bi(PS4)2 (1), Ag7Sn(PS4)3 (2), and Ag7Pb(PS4)3 (3), were obtained by solid-state synthesis. The structural frameworks of 2 and 3 feature an infinite 1-D interchiral double helix ∞1(Ag3P2S11), which is rare in inorganic compounds. Compound 3 undergoes a significant first-order structural phase transition from monoclinic to hexagonal at ∼204 °C. This can be ascribed to the significant mismatch in the expansion coefficients between Pb–S (Ag–S) and P–S bonds evaluated by bond valence theory. The three compounds are Ag+ ionic conductors, and Ag+ ion migration pathways are proposed by calculating maps of low bond valence mismatch. Moreover, the optical properties of the three compounds were studied, and electronic structure calculations were performed. The combination of second-order Jahn–Teller distorted d10 cation and lone-pair cation provides a new strategy to explore new metal thiophosphates with interesting structures and promising properties.
✓ 已验证
DOI
PubMed
高影响因子
MICROCHEMICAL JOURNAL
·
2024
·
IF 4.9
Yang Feng,Mengyi Yuan,Lan Zhang,Tingting Zhang,Shiying Wu,Lujie Li,Lingling Wang,Weihua Li,Rui Lu
This study reports the development of an electrostatic self-assembly surface-enhanced Raman scattering (SERS) substrate based on zeolitic imidazolate framework-8 (ZIF-8) decorated with silver nanoparticles (AgNPs). A seed-mediated growth method was employed to synthesize AgNPs with an average diameter of 30 nm, and a mild synthesis process was used to prepare ZIF-8 nanoparticles with an average diameter of 350 nm. The ZIF-8/Ag nanocomposites have been optimized and characterized using a variety of techniques. As a probe molecule, 4-aminothiophenol was used to evaluate the SERS performance of the ZIF-8/Ag nanocomposites, demonstrating low limit of detection to 8.32 × 10 −8 M, respectively. ZIF-8/Ag nanocomposites also demonstrated good signal reproducibility with a relative standard deviation of 12.5 % for 10 −6 M 4-aminothiophenol. Furthermore, the ZIF-8/Ag nanocomposites have successfully been used to detect 4-mercaptopyridine and the pesticide thiram in laboratory tap water with recoveries ranging from 87 % to 113 %. The ZIF-8/Ag nanocomposites were further investigated for their potential use as SERS substrates for the detection of thiram residues on the surface of apples. A finite difference time-domain simulation was also conducted to investigate the SERS enhancement mechanism of the ZIF-8/Ag nanocomposites.
✓ 已验证
产品关联
DOI
高影响因子
LANGMUIR
·
2024
·
IF 3.7
Tao Xue,Hui Li,Yuying Wang,Han Miao,Xinxin Li
Synthesizing catalyst supports with appropriate compositions and structures is crucial for reducing the sizes of metal nanoparticles and enhancing their catalytic activities. In this work, a series of monolithic hyper-cross-linked supports (HCP-CC) with hierarchical pores were synthesized. The monolithic structure facilitated easy operation in catalytic reactions, while the composition and structure of HCP-CC could be tailored simultaneously by utilizing the functional cross-linking agent cyanogen chloride. Furthermore, in situ loading of nano-Ag into HCP-CC resulted in the hybrid catalyst HCP-CC-Ag. The synergy of confinement and coordination effect controlled and limited the size of nano-Ag to approximately 3 nm, classifying them as ultrasmall nanoparticles, which ensured outstanding catalytic activity. This hybrid catalyst could improve the reaction rate constant to 0.423 min–1; it efficiently promoted the degradation of organic dye and exhibited great universality and recyclability, making it a potential heterogeneous catalyst for dye wastewater treatment.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ChemistrySelect
·
2024
·Vol. 9
·期 41
·e202402898
·
IF 1.9
Yuxian Wang,Pengfei Bai,Xian Sheng,Molan Qing,Yuanyang Yi,Zhidong Zhang,Ling Jiang,Liying Zhu
Graphical This study reports an environmentally friendly approach for the extracellular synthesis of Pd−Ag bimetallic nanoparticles (Pd−Ag BNPs) with small size by reduction of Pd and Ag ions using cell-free supernatant of Deinococcus wulumuqiensis . The application of as-prepared bionanocatalyst in catalytic degradation of pollutant dyes demonstrates that Pd−Ag BNPs have excellent degradation ability of 4-nitrophenol and Rhodamine. Catalytic reduction of organic pollutants using metal nanoparticles (MNPs) as nanocatalyst is a promising approach. The widespread application of MNPs have led to an increase demand for their production. The green biosynthesis of MNPs using microbes is becoming increasingly important as they are benign and environmentally friendly. In this work, Deinococcus wulumuqiensis ( D. wulumuqiensis ) with high resistance to stresses was applied for the green preparation of different MNPs, including palladium nanoparticles (Pd NPs), silver nanoparticles (Ag NPs), and Pd−Ag bimetallic nanoparticles (Pd−Ag BNPs). The resultant MNPs exhibited a face-centered cubic structure, with average size of 6.70 (Pd NPs), 6.24 (Ag NPs), and 6.13 nm (Pd−Ag BNPs), respectively. FT-IR spectra indicated that the proteins and polysaccharides expressed by D. wulumuqiensis could potentially contributed to the formation of MNPs. The application of as-prepared biocatalyst in catalytic degradation of pollutant dyes demonstrated that Pd−Ag BNPs had greater degradation ability of 4-nitrophenol (95.1 %) and Rhodamine B (85.1 %) than monometallic nanoparticles. The pseudo-first-order kinetics results further indicated the superior catalytic ability of Pd−Ag BNPs, with rate constant of 0.450±0.009 (4-nitrophenol) and 1.54×10 −2 min −1 (Rhodamine B), respectively. Thus, the present study confirms that D. wulumuqiensis represents a promising candidate for the biosynthesis of Pd-based nanoparticles with small size, which exhibited potential applications as bionanocatalyst in the degradation of water pollutants.
✓ 已验证
产品关联
DOI
高影响因子
ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2024
·
IF 10.8
Shengmao Chao,Chiara Valsecchi,Ji Sun,Hong Shao,Xinxia Li,Changyu Tang,Meikun Fan
The spontaneous generation of hydrogen peroxide (H2O2) within atmospheric microdroplets, such as raindrops and aerosols, plays a crucial role in various environmental processes including pollutant degradation and oxidative stress. However, quantifying hydroxyl radicals (•OH), essential for H2O2 formation, remains challenging due to their short lifespan and low concentration. This study addresses this gap by presenting a highly sensitive and selective surface-enhanced Raman scattering (SERS) nanosensor specifically designed for quantifying •OH within water microdroplets. Utilizing a phthalhydrazide (Phth) probe, the SERS technique enables rapid, interference-free detection of •OH at nanomolar concentrations. It achieves a linear detection range from 2 nM to 2 μM and a limit of detection as low as 0.34 nM. Importantly, the SERS sensor demonstrates robustness and accuracy within water microdroplets, paving the way for comprehensive mechanistic studies of H2O2 generation in the atmosphere. This innovative approach not only offers a powerful tool for environmental research but also holds potential for advancing our understanding of atmospheric H2O2 formation and its impact on air quality and pollutant degradation.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Dehe Fan,Shiji Zhang,Yumeng Li,Hua Bin,Ruopeng Li,Yaqiang Li,Maozhong An,Peixia Yang,Jinqiu Zhang
Copper-based tandem catalysts are effective candidates for yielding multi-carbon (C2+) products in electrochemical reduction of carbon dioxide (CO 2 RR). However, these catalysts still face a significant challenge regarding in the low selectivity for the production of a specific product. In this study, we report a high selectivity of 77.8 %±2 % at −1.0 V (vs RHE) for the production of C 2 H 4 by using a Cu 88 Ag 12 NW catalyst which is primarily prepared through a combined Cu-Ag co-deposition and wet chemical method, employing an attractive strategy focused on regulating the microenvironment over Cu-Ag nanowires. The experimental and computational studies show that the higher *CO coverage and lower intermediate adsorption energy are important reasons for achieving the high C 2 H 4 selectivity of Cu 88 Ag 12 NW catalyst. Comsol simulation results indicate that dense nanowires exhibit a nano-limiting effect on OH − ions, thereby leading to an increase in local pH and promoting coupling reactions. The catalyst demonstrates no noticeable decrease in current density or selectivity even after 12 h of continuous operation. The Cu-Ag nanowire composite exhibits remarkable catalytic activity, superior faradaic efficiency, excellent stability, and easy synthesis, which highlights its significant potential for electro-reducing carbon dioxide into valuable products.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2024
·
IF 4.3
Heng Guo,Hongji Li,Mengyang Xu,Juan Zhou,Dan Zhang,Dandan Wang,Wei Sun
In this study, a core–shell structured bimetallic nano-cube, Au@Ag NCs, was prepared by seed-mediated growth procedure. The array structure of Au@Ag NCs was achieved at the interface through the autonomous assembly technique at the three-phase boundary. Employing polydimethylsiloxane (PDMS) as a flexible carrier, the array structure was effortlessly transferred to the PDMS membrane, bypassing the need for rigid substrates through a simple “pasting” method. This yielded a highly flexible and transparent SERS substrate with an array structure (Au@Ag NCs/PDMS membrane, AAP). In order to promote the selective detection property to the practical samples, molecularly imprinted polymers (MIPs) were coated on the surface of membrane to prepare the imprinted membrane (Au@Ag NCs/PDMS-MIMs, AAP-MIMs). It was demonstrated from the results that the AAP-MIMs exhibited high SERS sensitivity, stability, and uniformity. Furthermore, the flexible substrate possessed commendable mechanical strength, and facilitated the detection of analytes on irregular surfaces. In summary, this substrate held promising potential for practical on-site detection and analysis of specific target substances.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）