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Coatings · 2019 ·Vol. 9 ·期 5 ·325 · IF 2.33

Doped PANI Coated Nano-Ag Electrode for Rapid In-Situ Detection of Bromide in Seawater

Qiujin Wang,Yifan Zhou,Jixue Zhou,Rongrong Wu,Jianbo Wu,Hao Zheng,Ying Ye,Yuanfeng Huang

In this paper, we successfully fabricated a novel bromide ion selective electrode (Br-ISE), which was coated by bromine ion doped polyaniline as sensitive film. Using Ag wire as the substrate, a uniform and dense nano-silver layer was electroplated to enhance the specific surface area of the electrode. Subsequently, a polyaniline (PANI) film was coated onto the electrode by cyclic voltammetry in a 0.3 M aniline and 1 M HCl solution and was in-situ doped by 0.1 M KBr solution. The morphology and performance of the electrode were characterized by scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS), and other electrochemical analysis methods, respectively. The prepared Br-ISE exhibited a wide linear dynamic range between 1.0 × 10−1and 1.0 × 10−7M with a near-Nernst slope of 57.33 mV/decade. In addition, the electrode possessed extremely fast response time (<1 s) and low impedance (300 Ω), high sensitivity, and good selectivity. The electrode potential drifted within 2 mV in 8 h. The lifespan was larger than three months.Keywords:nano-silver;electrode;bromide ion doped PANI;film;in-situ measurement

研究领域: 材料科学 · 环境科学
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ANALYTICA CHIMICA ACTA · 2018 · IF 5.123

Development of cerium oxide-based diffusive gradients in thin films technique for in-situ measurement of dissolved inorganic arsenic in waters

Feng Tan,Xiao Jiang,Xianliang Qiao,Daming Sun,Jinsuo Gao,Xie Quan,Jingwen Chen,Suyu Ren,Yi Wang

A diffusive gradients in thin films (DGT) method using a new high-capacity cerium oxide (CeO 2 ) binding gel, for the first time, was developed for measuring dissolved inorganic arsenic in freshwater and seawater . The capacities of the new CeO 2 binding gel were 682 μg and 375 μg for As III and As V , respectively. The masses of As III and As V accumulated by CeO 2 -DGT device increased linearly with time and agreed well with the theoretical value calculated by DGT equation. The arsenic accumulation by CeO 2 -DGT was independent of pH (4.05–9.04) and ionic strength (0.1–750 mM), and common anions including CO 3 2− , SO 4 2− , Cl − and PO 4 3− had no obvious interference. CeO 2 -DGT showed excellent long-term deployment performance in freshwater and synthetic seawater . Field trials with CeO 2 -DGT achieved successfully the time-weighted-average concentrations of total inorganic arsenic in reservoir water (1.38 ± 0.09 μg/L) and coastal seawater (0.45 ± 0.06 μg/L). The results were comparable to those measured by grab sampling. The proposed method was reliable and robust for in-situ measurements of dissolved inorganic arsenic in environmental waters.

研究领域: 环境化学 · 分析化学 · 水环境监测 · 环境地球化学 · 污染生态学
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FUEL · 2017 · IF 4.601

A new approach for the measurement of the volume expansion of a CO2 + n-dodecane mixture in a fused silica capillary cell by Raman spectroscopy

Junliang Wang,Shuyan Zhou,Ke Bei,I-Ming Chou,Chunmian Lin,Zhiyan Pan

This work developed a new method for measuring the volume expansion of a CO 2   +   n -dodecane mixture, using a fused silica capillary cell (FSCC), combined with a heating-cooling stage and a confocal Raman spectrometer. The cell was constructed on the micron scale to reduce the temperature gradient and reagent consumption. The results confirmed the feasibility of this method that using Raman spectra to verify phase equilibrium, a digital camera to record images of the CO 2   +   n -dodecane mixture and a micrometer to measure the volume, a section of water (water seal) between n -dodecane and gas phase to prevent n -dodecane from evaporating. It was shown that the volume expansion factor of the mixture increased with pressure going from 1.0 to 10.0   MPa, but decreased as the temperature was raised from 30 to 80   °C. In addition, a positive quadratic relationship ( R 2   >   0.99) was obtained between Raman peak intensity ratio and volume expansion factor, such that more volume expansion factors could be obtained according to the equations with measured Raman peak intensity ratio data. This experiment widens the ranges of temperature and pressure in the measurements of the volume expansion, and provides more volume expansion data for CO 2 -enhanced oil recovery.

研究领域: 物理化学 · 能源科学 · 油气开采 · 光谱分析 · 热力学
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Analytical Methods · 2025 · IF 2.6

Phosphomolybdenum blue-based diffusive gradients in thin-films (DGT) and digital imaging for in-situ measurement of dissolved reactive phosphorus in surface sediment porewater

Zhaoyang Gu,Yongming Huang,Beichen Lin,Kunde Lin

Current methods for determining dissolved reactive phosphorus (DRP) in sediment porewater mainly rely on ex-situ analysis, which can be labor-intensive and introduces errors due to changes in the concentration and morphology during sampling and transportation. Therefore, there is a clear need for in-situ measurement methods for DRP in sediment porewater. In this study, a novel in-situ analytical method was developed by combining diffusive gradients in thin-films (DGT) and digital imaging techniques, based on the classic phosphomolybdenum blue (PMB) method. During deployment, DRP in sediment porewater diffuses into the DGT device, while reducing reagent (ascorbic acid) from the diffusive gel simultaneously diffuses into the binding gel and reacts with ammonium molybdate, resulting in the formation of PMB compounds. The color of the PMB compounds was recorded in-situ using a digital imaging technique, and the resulting images were analyzed to calculate the concentration of DRP in surface sediment porewater. By using the new method, analytical data of DRP in surface sediment porewater could be quickly obtained in the field near real-time, without water sampling and any further sample treatment, transportation and instrumental analysis in laboratories. The key parameters including the loading procedure for colorimetric reagents in the gels, the concentrations of ammonium molybdate and ascorbic acid, the amount of C18, and the thickness of the C18 binding gel, were systematically optimized. The optimized method demonstrated a wide linear range (4 ‒ 1000 μmol L-1, R2=0.993), with satisfactory accuracy (-6.23% ‒ 8.68%, n = 3) and good precision (6.60% ‒ 13.46%, n = 3) at an exposure time of 60 min. The method also performed well across different salinities (0 ‒ 35) and in the presence of interfering ions (SiO32‒, AsO33‒, F‒, and S2‒). The method was successfully applied to both freshwater and seawater sediments, with results comparable to those obtained using traditional analytical methods. Overall, the proposed method provides a new strategy for in-situ determination of DRP in surface sediment porewater.

CAS / MDL: 110-18-9 110-26-9
研究领域: 环境分析化学 · 海洋与淡水沉积物分析 · 原位传感技术 · 比色检测 · 地球化学
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Nature Communications · 2022 ·Vol. 13 ·期 1 ·1-13 · IF 17.694

Promoting favorable interfacial properties in lithium-based batteries using chlorine-rich sulfide inorganic solid-state electrolytes

Zeng Dewu,Yao Jingming,Zhang Long,Xu Ruonan,Wang Shaojie,Yan Xinlin,Yu Chuang,Wang Lin

The use of inorganic solid-state electrolytes is considered a viable strategy for developing high-energy Li-based metal batteries. However, suppression of parasitic interfacial reactions and growth of unfavorable Li metal depositions upon cycling are challenging aspects and not yet fully addressed. Here, to better understand these phenomena, we investigate various sulfide inorganic solid electrolytes (SEs), i.e., Li 7− x PS 6− x Cl x ( x  = 0.6, 1.0, 1.3, 1.45, and 1.6), via ex situ and in situ physicochemical and electrochemical measurements. We found that the Cl distribution and the cooling process applied during the SE synthesis strongly influence the evolution of the Li|SE interface in terms of microstructure, interphase composition, and morphology. Indeed, for a SE with a moderate chlorine content (i.e., x  = 1.3) and obtained via a slow cooling process after sintering, the Cl atoms are located on the surface of the SE grains as interconnected LiCl nanoparticles that form an extended LiCl-based framework. This peculiar microstructure facilitates the migration of the Cl ions to the Li|SE interface during electrochemical cycling, thus, favouring the formation of a LiCl-rich interphase layer capable of improving the battery cycling performances.

研究领域: 材料科学 · 电化学 · 电池技术
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JOURNAL OF HAZARDOUS MATERIALS · 2023 · IF 13.6

Development and evaluation of diffusive gradients in thin-films technique with a novel titanium peroxide binding gel for in situ measurement of Tl in natural waters and sediments

Hongmei Deng,Meiling Liu,Zhaodong Liu,Minhua Su,Yue Gao,Danxing Yang,Yuxuan Liu,Liang Ma,Zhiqiang Yu,Tangfu Xiao,Jun Luo

Speciation of thallium (Tl) controls its fate and biogeochemical behaviors. Thus, a sensitive and accurately approach for Tl monitoring is of great demand due to its ultra-low concentration and sensitivity to redox change. In this study, diffusive gradients in thin-films technique (DGT) assembled with novel titanium peroxide (TP) binding gels (TP-DGT) was developed for in situ measurement of dissolved Tl(I) and Tl(III) in waters and sediments. Laboratory test showed a linear mass accumulation of Tl(I) and Tl(III) on the TP binding gels with the deployment time from 4 to 72 h. A fascinating performance of this novel DGT was achieved in a pH range of 4–9, ionic strength range of 0.1–200 mmol L −1 , and humic acid concentration of 0–30 mg L −1 with a low detection limit of 0.3 ng L −1 for Tl(I) and 0.6 ng L −1 for Tl(III). The TP binding gels own excellent stability (1–365 d) and high capacity (73.5 μg Tl disc −1 ) which are suitable for long-term monitoring. Field application in a river indicated that TP-DGT could work effectively, comparable to the grab sampling in waters. For the first time, the TP-DGT coupled with oxygen optode was successfully applied to map 2D distribution patterns of Tl and oxygen simultaneously in the rhizosphere of M. verticillatum L. This study confirms TP-DGT is a promising tool for routine monitoring of Tl in waters and for investigating biogeochemical processes of Tl in sediments.

研究领域: 环境科学 · 分析化学 · 地球化学
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