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Analytical Methods · 2017 ·Vol. 9 ·期 30 ·4471-4475 · IF 1.9

A low cost and rapid analytical technique for direct spectrophotometric determination of chromium in V–Cr–Ti alloys without a chromogenic agent

L. F. Tian,D. S. Zou,Y. C. Dai,L. L. Wang,W. Gao

Quantification of chromium in V–Cr–Ti ternary alloys, used as candidate structural materials for fusion reactors, is essential in view of its significant effect on the properties of these vanadium-based alloys. Various methods have already been used for the determination of chromium in common alloys, but most of these methods are based on complicated and expensive instruments or suffer from the serious matrix interference of vanadium. In this study, a simple, rapid and accurate spectrophotometric method was developed for the determination of chromium in V–Cr–Ti alloys without any prior separation and chromogenic agent. The alloy samples were dissolved in diluted sulphuric acid and concentrated nitric acid, and chromium was oxidized with persulphate in the presence of Ag(I) ions as a catalyst. After alkalization of the solution with sodium hydrate, greenish-yellow coloured chromate (CrO42−) ions were formed in the alkaline solution and had a maximum absorption peak at 374 nm. Beer's law was obeyed in the range of 0.15–12.0 μg mL−1 Cr(VI) at 374 nm and the molar absorptivity was 4.8 × 103 L mol−1 cm−1. All the variables were studied in order to optimize the analytical conditions. Vanadium and titanium seriously interfered with the determination of Cr(VI) and their interference can be eliminated by addition of ammonium tartrate. The proposed method is simple, fast, accurate and of low cost, and has been satisfactorily used for the determination of chromium in V–Cr–Ti alloys. The results are in good agreement with data given by inductively coupled plasma optical emission spectrometry (ICP-OES) and the relative standard deviation is found to be lower than 0.4%.

研究领域: 分析化学 · 材料科学
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ANALYTICAL SCIENCES · 2017 ·Vol. 33 ·期 8 ·963-967 · IF 1.228

Colorimetric Detection of Ascorbic Acid Based on the Trigger of Gold Nanoparticles Aggregation by Cr(III) Reduced from Cr(VI)

Sui Ning,Liu Fengya,Li Tailing,Wang Lina,Wang Tao,Liu Manhong,Yu William W.

Au nanoparticles (AuNPs) dispersed in water were stabilized by tripolyphosphate (P 3 O 10 5- ). When Cr 2 O 7 2- (Cr(VI)) was present, the AuNPs did not change; when Cr 3+ (Cr(III)) was present, the AuNPs would aggregate because of cooperative metal-ligand reaction. Aggregated AuNPs showed different color from the non-aggregated ones. Thus, a simple colorimetric assay was made using AuNPs-Cr(VI) to detect ascorbic acid (AA). Upon introducing AA to the AuNPs- Cr(VI) system, Cr(VI) was reduced to Cr(III), and the aggregation of AuNPs occurred. This colorimetric assay performed high selectivity and a linear concentration response in the range of 0.2 to 10 μM; its limit of detection was 0.15 μM.

CAS / MDL: 13548-38-4
研究领域: 分析化学 · 纳米科学 · 环境科学
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Scientific Reports · 2018 ·Vol. 8 ·期 1 ·1-14 · IF 4.122

Localization and Speciation of Chromium in Coptis chinensis Franch. using Synchrotron Radiation X-ray Technology and Laser Ablation ICP-MS

Huang Wenli,Jiao Jie,Ru Mei,Bai Zhenqing,Yuan Honglin,Bao Zhian,Liang Zongsuo

Coptis chinensis Franch. is one of the most important medicinal plants globally. However, this species contains relatively high concentrations of chromium (Cr) which potentially detrimental to human health. It is important to understand Cr localization and speciation in order to evaluate its accumulation and transportation mechanisms and minimize Cr transfer to humans. As little previous work in this area has been carried out, we utilized synchrotron radiation microscopic X-ray fluorescence (SR-μXRF) and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to spatially locate Cr, X-ray absorption near-edge spectroscopy (XANES) to analyze Cr speciation, and inductively coupled plasma mass spectrometry (ICP-MS) to detect Cr subcellular concentration. Micromapping results showed that Cr was distributed predominantly within the vascular cylinder, the periderm and some outer cortex, and the cortex and some vascular bundles in root, rhizome, and petiole, respectively. XANES data showed that Cr(VI) can be reduced to Cr(III) when grown with Cr(VI), and yielded a novel conclusion that this plant contain elemental chromium. ICP-MS data showed that Cr was primarily compartmentalized in cell walls in all tissues. The new insights on Cr accumulation in C. chinensis Franch. provide a theoretical basis for the evaluation of Cr in other medicinal plants.

研究领域: 植物学 · 环境科学 · 药用植物研究
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SURFACE & COATINGS TECHNOLOGY · 2021 · IF 4.158

Microstructure and flow accelerated corrosion resistance of Cr coatings electrodeposited in a trivalent chromium bath

Ying Wang,Yanhong Liu,Guangbin Li,Mingmin Zheng,Yusha Li,Anlei Zhang,Yingchun Zhang

In this study, Cr coatings were electrodeposited on carbon steel substrates by a trivalent Cr salt. The microstructure of the Cr coatings and their flow accelerated corrosion (FAC) resistance in simulated secondary circuit environments (10 MPa and 150 °C) of nuclear power plants were investigated. The results showed that the as-deposited coating was amorphous and crack-free. Annealing at 200 °C resulted in the decrease of Cr (OH) 3 and the increase of Cr and Cr 2 O 3 on the coating surface , which improved the corrosion resistance of the coating. The subsequent FAC test showed that the Cr coatings significantly improved the FAC resistance of the carbon steel substrate. The coating annealed at 200 °C exhibited better FAC resistance. The Cr-rich oxide film formed on the coatings was mainly Cr 2 O 3 , with a small amount of Cr and CrO 2 . Due to the galvanic effects caused by pinhole defects, abnormally grown annular deposits formed on the coating surface.

CAS / MDL: 10026-24-1
研究领域: 材料科学 · 腐蚀与防护
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CERAMICS INTERNATIONAL · 2021 · IF 4.527

Corrosion mechanism of magnesia-chrome and alumina-chrome refractories in E-scrap smelting

Zhiqian Yu,Zhihong Liu,Fengchun Ye,Longgong Xia

Pyrometallurgical processes have been widely recognised as the preferred technology for E-scrap recycling, and E-scrap smelting is usually accompanied by the formation of high-Al 2 O 3 -content slag. However, this slag can cause problems, such as refractory wear and even accelerated failure. Therefore, the corrosion mechanism of magnesia-chrome and alumina-chrome refractories in contact with FeO x -SiO 2 -CaO-Al 2 O 3 smelting slag was experimentally studied in the range of 1300–1400 °C, in air ( p O2  = 0.21 atm) and at p O2  = 10 -7  atm. The results showed that refractory-component dissolution and new phases formation were the major causes of refractory degradation. The dissolution of the refractory components increased along with both increasing temperature and decreasing Al 2 O 3 concentration in the initial slag. When decreasing the p O2 , the dissolution of MgO and Al 2 O 3 into the slag slowed down. New phases such as forsterite, anorthite, and spinel were detected at the interface between the slag and the bulk refractory. The formation of forsterite accelerated the refractory wear, whereas the newly formed (MgO,FeO)·(Cr 2 O 3 ,Fe 2 O 3 ,Al 2 O 3 ) spinel phase acted as a protective layer against further corrosion. A lower Al 2 O 3 concentration in the slag and a higher smelting temperature both densified the formed spinel layer. Additionally, a high oxygen partial pressure was beneficial to the formation of spinel in the magnesia-chrome refractory corrosion experiments. However, a low oxygen partial pressure was favourable for the formation of spinel on the surface of the alumina-chrome refractory materials . This study provides useful information for designing refractory materials and optimizing the processing parameters of E-scrap smelting.

CAS / MDL: 1317-61-9
研究领域: 材料科学 · 冶金工程
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2015 · IF 2.752

Red-to-blue colorimetric detection of chromium via Cr (III)-citrate chelating based on Tween 20-stabilized gold nanoparticles

Xiaokun Wang,Yingqin Wei,Shasha Wang,Lingxin Chen

In this work, a simple “red-to-blue” colorimetric method for highly sensitive and selective determination of Cr (III) and Cr (VI) was presented, which was based on the aggregation of Tween 20-stabilized gold nanoparticles (Tween 20-Au NPs). This strategy relied upon the distance-dependent optical properties of gold nanoparticles (Au NPs), strong chelating between Cr (III) and citrate, and the reduction of Cr (VI) to Cr (III) by ascorbic acid (AA). Cr (III) could chelate with citrate to form a stable Cr (III)-citrate complex and thereby induce the aggregation of Tween 20-Au NPs. Thus, the sensing of Cr (III) and Cr (VI) based on aggregation of Au NPs was developed with the color of the Au NPs changing from red to blue, which was readily seen by the naked eye. The color change and surface plasmon resonance (SPR) absorption were used to monitor Cr (III) and Cr (VI) levels. Under the optimal assay conditions, good linear relationship was obtained, and the detection limit of Cr (III) and Cr (VI) were 0.016   μM and 0.009   μM in standard aqueous solution, respectively. Furthermore, the colorimetric method exhibited a good selectivity over other metal ions and was successfully applied to detect Cr (III) and Cr (VI) in real water samples.

研究领域: 分析化学 · 环境科学 · 纳米技术
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Environmental Science & Technology Letters · 2017 · IF 5.308

Metal Respiratory Pathway-Independent Cr Isotope Fractionation during Cr(VI) Reduction by Shewanella oneidensis MR-1

Jun-Cheng Han,Guo-Jun Chen,Li-Ping Qin,Yang Mu

Cr isotope fractionation during microbial reduction processes is commonly recognized as a promising tool in biogeochemistry and bioremediation. However, the mechanism of Cr isotope fractionation during microbial reduction is poorly understood. In this work, the relationship between the bacterial respiratory pathway and Cr isotope fractionation was investigated in Shewanella oneidensis MR-1. For comparison with the wild type, a mutant strain (ΔomcA/ΔmtrC) with a deficiency in extracellular Cr(VI) reduction was constructed by deleting the omcA and mtrC genes, which encode the terminal reductase during extracellular reduction. The magnitudes of Cr isotope fractionation (ε) for Cr(VI) reduction by the wild type and ΔomcA/ΔmtrC were −2.42 ± 0.68‰ and −2.70 ± 0.22‰, respectively. Surprisingly, the ε values were not significantly different between the two strains. This suggests that isotope fractionation is independent of the metal respiratory pathway during Cr(VI) reduction by S. oneidensis MR-1. Moreover, a three-step Cr isotope fractionation model that includes uptake, reduction, and efflux was proposed to exist during intracellular Cr(VI) reduction by S. oneidensis MR-1. The developed model provides a better understanding of Cr isotope fractionation during microbial reduction.

CAS / MDL: 7789-00-6
研究领域: 生物地球化学 · 环境微生物学
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WATER AIR AND SOIL POLLUTION · 2017 ·Vol. 228 ·期 11 ·1-10 · IF 1.702

Photochemically Induced Electron Transfer: Simultaneously Decolorizing Dye and Reducing Cr(VI)

Laipan Minwang,Fu Haoyang,Zhu Runliang,Rivera Linda,Zhu Gangqiang,Zhu Jianxi,He Hongping

Hexavalent chromium (Cr(VI)) and dyes are of particular environmental concern and need to be removed from water urgently due to their high toxicity. Herein, we explored the possibility of electron transferring from dye Orange II (OII) to Cr(VI) under UV and simulated solar light irradiation, expecting to simultaneously decolorize dyes and reduce Cr(VI). Experimental results show that light irradiation can partially decolorize OII but has no ability to reduce Cr(VI) in solution only with OII or Cr(VI). However, both dyes and Cr(VI) can effectively and simultaneously be decolorized and reduced in the solution containing both OII and Cr(VI) under light irradiation, and a low pH level and high OII/Cr(VI) concentration ratio significantly favor the co-removal. Additionally, insoluble organo–Cr(III) complexes identified by FTIR and XPS characterization were generated during the reaction. These complexes are beneficial to the removal of chromium and total organic carbon from water. The possible degradation pathway of OII is further proposed based on the detection of degraded products by GC-MS analysis. The results of this work offer an approach for simultaneously removing multiple contaminants.

研究领域: 环境科学 · 化学
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JOURNAL OF THE INDIAN CHEMICAL SOCIETY · 2021 · IF 0.284

Improvement of hydrothermal stability and chrome uptake of leather: Amino-terminated hyper-branched polymer as high exhausted tanning auxiliary

Qi Yao,Hualin Chen,Youyi Chen,Lianlong Zhan

Carboxyl-terminated hyper-branched polyester is extensively used as high exhaustion chrome tanning auxiliary owing to its strong coordination ability with trivalent chrome. Owing to lower electronegativity of N than O, the coordination ability with trivalent chrome for hyper-branched polyamide is stronger than polyester. Herein, in this paper, an amino-terminated hyper-branched polyamide (HBPN) is synthesized and used as high exhaustion chrome in tanning of pickling pigskin (HBPN–Cr). The effects of utilization of HBPN in denaturation temperature, shrinkage temperature, chrome uptake, and microstructure structure of wet-blue leather are studied. Moreover, the anti-oxidation stability of wet-blue leather is preliminary studied by heat treatment. The results show that incorporation of 1% HBPN in pickling process can significantly improve chrome uptake to 83.32%. The hydrothermal stability of wet-blue leather is improved due to the formation of higher crosslinking degree of collagen fibers. In addition, for the wet-blue leather without unsaturated fatliquoring agent, through heat treatment, hexavalent chrome does not appear after 24 ​h heat treatment. On the contrary, the chrome complex changes from hydroxyl copolymerization to more stable oxygen copolymerization or chrome oxide for C–Cr and HBPN-Cr tanned leather, respectively. These results will build a data support for the further study of hyper-branched polymer chrome tanning auxiliaries.

CAS / MDL: 107-15-3 110-26-9
研究领域: 材料科学 · 化学工程 · 皮革加工
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MICROCHIMICA ACTA · 2022 ·Vol. 189 ·期 12 ·1-10 · IF 6.408

A dual-readout paper-based analytical device for the simultaneous determination of hexavalent Cr and total Cr

An Yingying,Wang Wan,Lv Qing,Zhang Qing,Wang Xiayan

A paper-based analytical device (PAD) is presented with colorimetric/electrochemical dual readouts for the simultaneous sensing of total chromium (Cr) and hexavalent chromium (Cr(VI)). This device consists of a homemade three-electrode system and a patterned paper chip, integrating multiple functions including electrochemical detection, fluid driving, online oxidation, and colorimetric detection. The fiberglass filter paper with a hydrophilic microchannel was used to achieve self-driving fluidics without external equipment. One end of the microchannel was integrated with a homemade three-electrode system to achieve sample loading and electrochemical detection. The middle region on the microchannel was modified with oxidizing reagents to perform online pretreatment, and the yield of Cr(III) oxidation can reach 97.9%, ensuring reliable colorimetric detection of total Cr at another end of the microchannel modified with chromogenic agents. With this device, the signals of Cr(VI) (the signal peak at 0.29 V vs. Ag/AgCl) and total Cr can be obtained in one single injection. After optimization, the limit of detection (LOD) of Cr(VI) and total Cr were 0.01 mg L −1 and 0.06 mg L −1 and the linear ranges were 0.05–3.0 mg L −1 and 0.2–3.0 mg L −1 , respectively. The relative standard deviations (RSD) of the electrochemical testing of Cr(VI) results were in a range 1.3%–8.7% ( n  = 3), and the RSD values of the colorimetric testing of total Cr were between 0.7–9.2% ( n  = 3). The device’s reliability was demonstrated by performing the practical speciation of Cr in tap water, river water, and electroplating wastewater while the recoveries obtained using the present method were in the range 93.5–106%. Overall, the proposed device provides high application prospect in the on-site rapid Cr speciation. Graphical abstract

研究领域: 环境科学 · 分析化学
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2020 ·Vol. 27 ·期 14 ·16745-16753 · IF 3.056

Shewanella oneidensis MR-1 impregnated Ca-alginate capsule for efficient Cr(VI) reduction and Cr(III) adsorption

Yu Cheng,Zhang Yi,Fang Yu,Tan Yujie,Dai Ke,Liu Shilin,Huang Qiaoyun

Shewanella oneidensis MR-1 (MR-1)-impregnated alginate capsules with 3D porous structure were prepared through cation crossing-linking and was used for the Cr(VI) reduction and removal. After being encapsulated by alginate, the endurance of the MR-1 was largely enhanced under conditions of high Cr(VI) concentrations (up to 4 mM) and low pH (pH 5). The Cr(VI) reduction over the MR-1-impregnated alginate capsules could be fitted by pseudo first-order kinetic model. With the Cr(VI) initial concentration increasing from 1 to 4 mM, the first-order rate constant for the encapsulated MR-1 ( k capsules ) and free cells ( k cells ) fell by 26.3% and 82.4%, respectively. At pH 5, the k capsules value was 0.19 h − 1 , which was about 3.7 times higher than k cells . Moreover, the encapsulated MR-1 held 90.5% of the Cr(VI) reduction ability after 15 days of resting time, while the free MR-1 held 19.7%. After bioreduction, 73.6% of total chromium was adsorbed on the MR-1 impregnated Ca-alginate capsules. XPS results showed 85% of the adsorbed chromium was Cr(III). The mechanism for chromium removal over the MR-1-impregnated Ca-alginate capsules was proposed with the following steps: (1) Cr(VI) was bioreduced via the encapsulated MR-1; (2) the reduced soluble Cr(III) was adsorbed by alginate selectively. In the study, the Ca-alginate shell of the cabbage-like MR-1 impregnated capsules could be a shelter for encapsulated MR-1 to endure unfavorable conditions (e.g., low pH and high concentration of Cr(VI)) and immobilize the soluble chromium. Considering the obtained capsules derived from biomolecules were environment-friendly, the MR-1-impregnated Ca-alginate capsules were potential for the application in the remediation of environmental pollution. Graphical abstract

研究领域: 环境科学 · 微生物学
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Toxics · 2025 ·Vol. 13 ·期 4 ·262 · IF 4.1

A Study on the Oxidation Performance of Soil Chromium with Acid Birnessite and Cryptomelane

Wei Zhang,Huan Yang,Shaohong You,Xia Zhong,Pingping Jiang,Xudong Lan,Rui Ma

Current research focuses more on redox of toxic Cr(VI), with less attention to Cr(III) changes in flooded soil. First, the structure of acid birnessite and cryptomelane was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and other test methods. This study investigated farmland soil in Yuxi, Yunnan Province, under flooding stress induced by the addition of two distinct concentrations of manganese oxides. Throughout the experiment, key physicochemical properties of the soil—including pH, redox potential (Eh), Cr(VI) concentration, and chromium speciation—were systematically measured and analyzed. Structural characterization demonstrated distinct morphological and surface area properties. Specifically, acid birnessite, with petal-like stacked spheres, has a specific surface area of 103.76 m2/g, while cryptomelane, strip-shaped, has an area of 95.92 m2/g. The submergence experiment yielded the following phenomena: (1) During the 60-day flooding experiment, soil amended with 0.5% or 1% acid birnessite or cryptomelane exhibited an increase in Eh compared to the control group. (2) At the end of the 60-day submergence period, the Cr(VI) concentration in the soil treated with 1% acid birnessite increased by 2.4 times compared to the control group. In addition, after 60 days, Cr(VI) concentrations in the soil exceeded 5 mg/L in soils with manganese oxide added to them. This study evaluates how manganese oxides oxidize Cr(III), aiding in assessing their environmental risks and long-term impacts on metal transformation. The findings help predict chromium behavior in farm soils and guide remediation strategies.

CAS / MDL: 10034-96-5
研究领域: 环境科学 · 土壤学
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