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Cr(VI)
Nanomaterials · 2018 ·Vol. 8 ·期 7 ·472 · IF 3.504

Facile Synthesis of Novel CaIn2S4/ZnIn2S4 Composites with Efficient Performance for Photocatalytic Reduction of Cr(VI) under Simulated Sunlight Irradiation

Siyu Xu,Jun Dai,Juan Yang,Jun You,Jingyi Hao

A series of novel and efficient heterostructured composites CaIn2S4/ZnIn2S4have been synthesized using a facile hydrothermal method. XRD patterns indicate the as-prepared catalysts are two-phase composites of cubic phase CaIn2S4and hexagonal phase ZnIn2S4. FESEM (field emission scanning electron microscope) images display that the synthesized composites are composed of flower-like microspheres with wide diameter distribution. UV–Vis diffuse reflectance spectra (DRS) show that the optical absorption edges of the CaIn2S4/ZnIn2S4composites shift toward longer wavelengths with the increase of the CaIn2S4component. The photocatalytic activities of the as-synthesized composites are investigated by using the aqueous-phase Cr(VI) reduction under simulated sunlight irradiation. This is the first report on the application of the CaIn2S4/ZnIn2S4composites as stable and efficient photocatalysts for the Cr(VI) reduction. The fabricated CaIn2S4/ZnIn2S4composites possess higher photocatalytic performance in comparison with pristine CaIn2S4or ZnIn2S4. The CaIn2S4/ZnIn2S4composite with a CaIn2S4molar content of 30% exhibits the optimum photocatalytic activity. The primary reason for the significantly enhanced photoreduction activity is proved to be the substantially improved separation efficiency of photogenerated electrons/holes caused by forming the CaIn2S4/ZnIn2S4heterostructured composites. The efficient charge separation can be evidenced by steady-state photoluminescence spectra (PLs) and transient photocurrent response. Based on the charge transfer between CaIn2S4and ZnIn2S4, an enhancement mechanism of photocatalytic activity and stability for the Cr(VI) reduction is proposed.Keywords:CaIn2S4/ZnIn2S4composites;Cr(VI);photocatalysis;simulated sunlight;hydrothermal method

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RSC Advances · 2019 ·Vol. 9 ·期 19 ·10958-10965 · IF 3.049

Highly selective and sensitive probes for the detection of Cr(VI) in aqueous solutions using diglycolic acid-functionalized Au nanoparticles

Yang Zhang,Ruixi Bai,Zhigang Zhao,Qiuxia Liao,Peng Chen,Wanghuan Guo,Chunqing Cai,Fan Yang

In this study, a variety of diglycolic acid-functionalized gold nanoparticle (Au NP) probes are reported, which are highly sensitive for the detection of chromium ions, Cr(VI) ions, at low concentrations in aqueous solutions based on the application of surface plasmon resonance (SPR) theory. Due to its outstanding affinity for Cr(VI) ions, the capped diglycolic acid would induce the aggregation of the NP probes upon encountering them; this was evidenced by the obvious red-shifting of the SPR peak and the enlarged size of the NPs. For the same reason, the selectivity of the probe for Cr(VI) against other heavy metal ions was found to be remarkable. Under optimized conditions, the probe showed the limit of detection (LOD) of 0.32 ppb for Cr(VI) and a linear detection scale ranging from 0.32 ppb to 0.1 ppm. To the best of our knowledge, this is probably the lowest LOD reported for Cr(VI) detection among those of the methods based on SPR.

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ANALYTICAL AND BIOANALYTICAL CHEMISTRY · 2019 ·Vol. 411 ·期 27 ·7165-7175 · IF 3.286

Selective fluorescence sensor based on ion-imprinted polymer-modified quantum dots for trace detection of Cr(VI) in aqueous solution

Zhang Meng Yuan,Huang Ren Feng,Ma Xiao Guo,Guo Li Hui,Wang Ying,Fan Yin Ming

A new fluorescence sensor (QDs-IIP), based on ion-imprinted polymers (IIP) as recognition element and Mn-doped ZnS quantum dots (QDs) as fluorophore, was synthesized for the selective and sensitive determination of hexavalent chromium (Cr(VI)) ions. The QD was first coated by SiO 2 layer, and then modified with Cr(VI)-imprinted polymer. Several parameters affecting fluorescence intensity such as tetraethylorthosilicate (TEOS) volume, ZnS:Mn@SiO 2 amount, and radiation time were investigated and optimized. The QDs-IIP was characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR), transmission electron microscope (TEM), and scanning electron microscope (SEM). Furthermore, the fluorescence quenching mechanism was investigated by using UV-VIS and fluorescence spectrophotometer, and it was found that internal filtration effect was the main fluorescence quenching mechanism. The relative fluorescence intensity (F 0 /F) increased linearly with the increase of Cr(VI) concentration in the range of 20 μg L −1 –1.0 mg L −1 . The QDs-IIP sensor showed high recognition selectivity for Cr(VI) in comparison with the QDs-NIP sensor with an imprinting factor (IF) of 2.53, and it could be reused 5 times. In addition, an analytical method of Cr(VI) based on the QDs-IIP sensor was established with a limit of detection of 5.48 μg L −1 , and was then applied to actual water samples with satisfactory results. Therefore, QDs-IIP can be deemed as a practicable fluorescent sensor for trace Cr(VI) detection. Graphical abstract

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ACS Applied Bio Materials · 2024 · IF 4.6

3D-Printed Fluorescent Hydrogel Consisting of Conjugated Polymer and Biomacromolecule for Fast and Sensitive Detection of Cr(VI) in Vegetables

Xingli Ding,Li Sheng,Jianming Zhang,Ge Zhang,Qi Gu,Yu Li,Long Zhang,Min Ji

Portable fluorescent film sensors offer a solution to the contamination issue in homogeneous sensor detection systems. However, their special structure leads to low sensitivity and a long response time, resulting in a significant scientific challenge limiting their development and application. In this work, we propose a dual design strategy to prepare highly sensitive film sensors for rapidly detecting Cr2O72–. Specifically, P(Fmoc-Osu)-SA hydrogel films were developed by integrating the biological macromolecule sodium alginate (SA) with the conjugated polymer poly(N-(9-Fluorenylmethoxycarbonyloxy)succinimide) (P(Fmoc-Osu)), using both mold and inkjet 3D printing methods. The “molecular wire effect” of the sensing unit P(Fmoc-Osu) and the water channel within the film substrate are responsible for the improved sensitivity and the reduced response time of this thin film sensor. P(Fmoc-Osu)-SA hydrogel films prepared by these two methods can rapidly detect Cr2O72– with limits of detection of 1.18 and 0.078 nM, respectively. Considering that 3D-printed hydrogel films can be tailored to different shapes according to detection needs, the P(Fmoc-Osu)-SA hydrogel films produced from this method were effectively applied in vegetable samples. This study provides an innovative and effective strategy for the development of biocompatible hydrogel sensors that offer the potential for determining trace amounts of Cr2O72– in agriculture.

CAS / MDL: 82911-69-1 9005-38-3
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2025 · IF 8.5

Construction of carbon dot-embedded fluorescent hydrogels based on oxidized gum arabic-gelatin Schiff base for Cr(VI) detection applications

Meng Zhou,Miaomiao Chen,Yunyun Wang,Caihong Mao,Yu Zhang,Junmei Liu,Xikun Zhang,Shujie Pang,Xudong Yang

In this study, a novel nitrogen-doped carbon quantum dot/oxidized gum arabic-gelatin-based fluorescent probe (NAH) was prepared using gelatin (GL) and gum arabic (AG) biomolecules. The primary network structure of this hydrogel consisted of polyacrylamide (PAM), while a secondary network structure was constructed between oxidized gum arabic and gelatin through the reaction of the Schiff base, which significantly enhanced the mechanical properties, the stress and strain of NAH reached 266.47 KPa and 2175.75 %. Nitrogen-doped carbon dots (NCDs) with yellow fluorescence emission properties were synthesized by hydrothermal method using salicylic acid as the carbon source and o -phenylenediamine as the nitrogen source. The fluorescent sensor obtained by compounding NCDs with hydrogel was able to selectively detect Cr(VI). The linear range of its detection was 0–90 μM, and the detection limit was 0.19 μM. The maximum theoretical adsorption capacity of the NAH hydrogel was 169.4 mg/g, and its adsorption isotherm conformed to the Langmuir adsorption isotherm model, and the adsorption kinetics conformed to the quasi-secondary kinetic model. Compared with the NCDs solution, the NAH hydrogel showed superior comprehensive performance, especially in solving the problem of recovery of NCDs. Meanwhile, this hydrogel provides an effective insight into the efficient detection and adsorption of environmental pollutants.

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MICROPOROUS AND MESOPOROUS MATERIALS · 2016 · IF 3.349

A novel CoFe layered double hydroxides adsorbent: High adsorption amount for methyl orange dye and fast removal of Cr(VI)

Faling Ling,Liang Fang,Yi Lu,Jiemei Gao,Fang Wu,Miao Zhou,Baoshan Hu

CoFe-nitrate-layered double hydroxides (LDHs) with Co 2+ /Fe 3+ molar ratios of 2, 3 and 4 were synthesized by a simple co-precipitation method. The as-prepared CoFe-LDHs exhibited a high adsorption activity to the methyl orange (MO) dye and Cr(VI). The adsorption characteristics including adsorption kinetics and isothermals were investigated. Structure analysis of the as-synthesized LDHs before and after adsorption revealed that adsorption proceeds in two processes: external surface adsorption and interlayer anion exchange. The results of MO adsorption experiments showed that LDHs with Co 2+ /Fe 3+ molar ratios of 4 worked best with the largest MO adsorption amount up to 1290 mg/g at an initial concentration of 300 mg/L due to the porous structures. We have also noted that Cr(VI) in a range of 2–25 mg/L can be quickly removed with the maximum adsorption capacity of 27.62 mg/g in the initial 5 min, much faster than other LDH materials. Therefore, CoFe-LDHs are potential cost-effective adsorbents for both MO dye and Cr(VI).

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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
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JOURNAL OF HAZARDOUS MATERIALS · 2015 · IF 4.529

MIL-53(Fe) as a highly efficient bifunctional photocatalyst for the simultaneous reduction of Cr(VI) and oxidation of dyes

Ruowen Liang,Fenfen Jing,Lijuan Shen,Na Qin,Ling Wu

A bifunctional photocatalyst-Fe-benzenedicarboxylate (MIL-53(Fe)) has been synthesized successfully via a facile solvothermal method. The resulting MIL-53(Fe) photocatalyst exhibited an excellent visible light ( λ   ≥   420   nm) photocatalytic activity for the reduction of Cr(VI), the reduction rate have reached about 100% after 40   min of visible light irradiation, which has been more efficient than that of N-doped TiO 2 (85%) under identical experimental conditions. Further experimental results have revealed that the photocatalytic activity of MIL-53(Fe) for the reduction of Cr(VI) can be drastically affected by the pH value of the reaction solution, the hole scavenger and atmosphere. Moreover, MIL-53(Fe) has exhibited considerable photocatalytic activity in the mixed systems (Cr(VI)/dyes). After 6   h of visible light illumination, the reduction ratio of Cr(VI) and the degradation ratio of dyes have been exceed 60% and 80%, respectively. More significantly, the synergistic effect can also be found during the process of photocatalytic treatment of Cr(VI) contained wastewater under the same photocatalytic reaction conditions, which makes it a potential candidate for environmental restoration. Finally, a possible reaction mechanism has also been investigated in detail.

CAS / MDL: 10025-77-1
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WATER SCIENCE AND TECHNOLOGY · 2024 ·Vol. 89 ·期 9 ·2384-2395 · IF 2.5

Enhanced biodegradation of phenol under Cr(VI) stress by microbial collaboration and potential application of machine learning for phenol biodegradation

Bing Wenrong,Li Xinyu,Liang Mingzhao,Zhou Xu,Zhang Jianfeng,Liang Jing

View large Download slide View large Download slide Close modal Cr(VI) and phenol commonly coexist in wastewater, posing a great threat to the environment and human health. However, it is still a challenge for microorganisms to degrade phenol under high Cr(VI) stress. In this study, the phenol-degrading strain Bacillus cereus ZWB3 was co-cultured with the Cr(VI)-reducing strain Bacillus licheniformis MZ-1 to enhance phenol biodegradation under Cr(Ⅵ) stress. Compared with phenol-degrading strain ZWB3, which has weak tolerance to Cr(Ⅵ), and Cr(Ⅵ)-reducing strain MZ-1, which has no phenol-degrading ability, the co-culture of two strains could significantly increase the degraded rate and capacity of phenol. In addition, the co-cultured strains exhibited phenol degradation ability over a wide pH range (7–10). The reduced content of intracellular proteins and polysaccharides produced by the co-cultured strains contributed to the enhancement of phenol degradation and Cr(Ⅵ) tolerance. The determination coefficients R 2 , RMSE, and MAPE showed that the BP-ANN model could predict the degradation of phenol under various conditions, which saved time and economic cost. The metabolic pathway of microbial degradation of phenol was deduced by metabolic analysis. This study provides a valuable strategy for wastewater treatment containing Cr(Ⅵ) and phenol. Co-culture can degrade phenol under high concentrations of Cr(VI). Co-culture improves the degraded rate and concentration of phenol under Cr(VI) stress. Co-culture synergistically enhances the ability to resist phenol and Cr(VI) toxicity. BP-ANN predicted the degradation of phenol under different conditions.

CAS / MDL: 108-95-2
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Enhanced photocatalytic reduction of Cr (VI) using porous hierarchical Bi2O3/Bi2S3 high-low heterojunctions: Novel strategies and charge transfer mechanisms

Yan Sang,Jingwei Xue,Junjie Hu,Peng Zhang,Fugang Zhao,Yanping He

High-low heterojunctions derived from metal-organic frameworks (MOFs) have promising applications in photocatalytic wastewater treatment because of their high photo-redox ability and boosted charge separation efficiency. Herein, Bi-MOF derived porous hierarchical Bi 2 O 3 /Bi 2 S 3 nanoflower-like heterojunctions were prepared by the calcination-hydrothermal method. The optimized Bi 2 O 3 /Bi 2 S 3 -2 composite showed a higher degradation rate of Cr (VI) (99.79 % in 30 min) than the pure substance. Moreover, comprehensive studies were conducted on the kinetics, stability and recycling of Bi 2 O 3 /Bi 2 S 3 , as well as optical characteristics . The active species trapping experiments confirmed that e - plays a dominant role in the elimination of Cr (VI). These findings provided novel strategies for construction of porous hierarchical heterojunctions with advanced visible-light-induced degradation performance. The enhanced photo-degradation efficiency of the optimal nanocomposite was assigned to the higher visible-light absorbance, separation of photogenerated carriers, reduced recombination of photo-induced carriers, and enhanced redox capability owing to the construction of porous hierarchical heterojunctions amongst the components.

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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2024 · IF 4.3

Fe-doping green fluorescent carbon dots via co-electrolysis of chrysoidine G and potassium ferrocyanide for sensitive Cr(VI) detection

Tiantian Long,Hongmei Luo,Hongchen Li,Jingbo Sun,Yang Wang,Jiaquan Zhou,Yi Chen,Dong Xu

In this study, we aimed to synthesis of Fe-doping green fluorescent carbon dots (G-CDs) through the co-electrolysis of chrysoidine G and potassium ferrocyanide for Cr(VI) detection. The use of potassium ferrocyanide improves the quantum yield and sensing performance of G-CDs toward Cr(VI). The G-CDs have a maximum excitation wavelength of 308 nm and an emission wavelength of 510 nm. Comprehensive analyses including Raman, FT-IR, and XPS provided insights into the chemical structure and composition of the G-CDs. Under optimal conditions, G-CDs demonstrated concentration-dependent quenching upon interaction with Cr(VI). A linear relationship within the range of 0.25–100 µM was established with a calibration equation of ΔF/F0 = 0.005 + 0.015C Cr(VI) , yielding an R 2 value of 0.996 and a limit of detection of 0.15 μM. The applicability of the G-CDs method was demonstrated by successful Cr(VI) detection in water samples with recovery rates ranging from 98.8 % to 100.1 % and relative standard deviation within 3.0 %. The fluorescence lifetime and Zeta potential measurements confirmed that the mechanism was via a static quenching process, while redox reaction, nanoparticle aggregation, and surface charge variation also played significant roles.

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LANGMUIR · 2024 · IF 3.7

Construction of the Z-Scheme Heterogeneous HKUST-1/BiVO4 Nanorod Composite for Enhanced Piezo-Photocatalytic Reduction Performance of Cr(VI)

Qiqi Huang,Fuxiao Zhu,Feiyan Xiao,Gongliang Zhang,Hongman Hou,Jingran Bi,Shuang Yan,Hongshun Hao

In recent years, piezo-photocatalysis has become a promising strategy for solving environmental pollution problems by adding additional mechanical energy to the photocatalysis process. This work reported the effective synthesis of a variety of HKUST-1/BiVO4 heterogeneous materials by combining monoclinic BiVO4 and porous HKUST-1 semiconductors. The piezo-photocatalytic properties of HKUST-1/BiVO4 were studied by the reduction of hexavalent chromium (Cr(VI)) under visible-light irradiation and ultrasonic waves. In the piezo-photocatalysis process, the best reduction rates among as-prepared HKUST-1/BiVO4 composites were up to 96.20% of 10 ppm Cr(VI) solution, which was approximately 1.80 times that under visible light and about 4.13 times that under ultrasound. Under the action of the piezoelectric potential, the availability of free radicals increased the reduction rate of Cr(VI) and reached a synergistic effect of 1.14-fold.

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