Arabian Journal of Chemistry
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2020
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IF 4.762
Zefeng Yu,Weifeng Song,Jiayao Li,Qiuhua Li
In this paper, a metakaolin-based mesoporous geopolymer (GP-CTAB) was used as adsorbent for Cu(II) and Cr(VI) through a novel and simple synthetic route using cetyltrimethylammonium bromide (CTAB) as an organic modifier. The application of GP-CTAB for the simultaneous removal of metal anions and cations in aqueous solution was studied for the first time. The results of X-ray diffraction (XRD) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, Brunauer, Emmett and Teller (BET), and Barrett, Joyner, and Halenda (BJH) methods indicate that GP-CTAB is still geopolymer even in the presence of quaternary ammonium salt cations. The material was tested to simultaneously adsorb Cu(II) and Cr(VI) from an aqueous solution. The results show that GP-CTAB can adsorb anions simultaneously without sacrificing the adsorption properties of heavy metal cations, which is superior to conventional geopolymers. The maximum theoretical adsorption capacity of GP-CTAB for Cu(II) and Cr(VI) was 108.2 mg/g and 95.3 mg/g in the binary system, respectively. It was also found that the presence of Cu(II) in the solution promoted the adsorption of Cr(VI). Given this characteristic of GP-CTAB, it has shown great application prospects in the prevention and control of heavy metal pollution.
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Environmental Progress & Sustainable Energy
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2020
·Vol. 40
·期 1
·e13479
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IF 1.989
Zhengjiang Liu,Anqi Wang,Qiancheng Zhang,Juming Liu,Huiyan Ma,Di Li,Lei Xing
Sensitized kaolinite with improved visible-light catalytic activity was prepared via a facile in-situ growth of nanosized Cu-TiO 2 on the surface of the sulfated kaolinite impregnated in Cu-TiO 2 sol. The as-prepared photocatalysts were characterized in terms of various techniques. The transmission electron microscope and energy dispersive spectrometer results revealed that Cu-TiO 2 could grow on the surface of the pretreated kaolinite and the aggregation of Cu-TiO 2 was successfully inhibited. The X-ray photoelectron spectrum confirmed the formation of Al O Ti bonds between Cu-TiO 2 and sulfated kaolinite in the sensitized kaolinite composite. The sensitized kaolinite composite exhibited significantly improved performance in the degradation of Rhodamine B (RhB), leading to about 87% of RhB degradation in 180 min, which is superior to that of the kaolinite, calcined kaolin, and sulfated calcined kaolin under visible-light irradiation. The superior photodegradation activity of the sensitized kaolinite composite was primarily attributed to the synergetic effect of Cu-TiO 2 sensitization and sulfation, resulting from the efficient transfer and separation of the photo-induced charge carriers between Cu-TiO 2 and kaolinite.
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JOURNAL OF HAZARDOUS MATERIALS
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2020
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IF 9.038
Sisi Zhang,Jiayi Zhu,Xiwang Zhang,Runliang Zhu,Fei Ge,Yin Xu
Zero-valent Cu-Fe bimetallic porous carbon materials were successfully applied to remediate organic wastewater. In this work, we successfully recycled the layered double hydroxides (LDHs) adsorbed with Orange II (OII) to form a zero-valent Cu-Fe bimetallic porous carbon material (CuFe/Carbon). The characterization results showed that CuFe/Carbon was a zero-valent Cu-Fe bimetallic porous graphene-like carbon material. In the course of the experiment, we found that aeration condition had a great influence on the activity of CuFe/Carbon. The removal efficiency of nitrobenzene (NB) was 100 % in nitrogen system and 48 % in air system. The active species of O 2 − and O H was formed under air condition, while there was no active species under nitrogen condition. NB was reduced to aniline directly under nitrogen condition. We proposed there were reduction and oxidation mechanisms under different aeration conditions. This work mainly investigated the conversion process of a novel material under different reaction conditions, which provided theoretical support for the removal of organic matters.
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2020
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IF 16.683
Lixia Li,Juanhua Kong,Huimin Zhang,Sijie Liu,Qiang Zeng,Yaqin Zhang,Hao Ma,Hongyan He,Jinxing Long,Xuehui Li
The catalytic depolymerization process for lignin to produce value added chemicals is often challenged by the limited mass transfer over heterogeneous catalysts, the complex aromatic biopolymer structures, and the high recalcitrance of C C bonds. Herein, a series of hierarchical MFI nanosheets (MFI-ns) supported metal oxide catalysts have been designed and used for the selectively oxidative cleavage of organosolv lignin. As expected, 81.6 % conversion of lignin can be achieved over 15Ce-5Cu/MFI-ns with 294.0 mg g −1 yield of volatile products, including 180.9 mg g −1 of diethyl maleate. Quantum chemistry calculation coupled with static adsorption measurements shows that the superior catalytic activities of these catalysts are ascribed to the favorable mass transport of lignin to the active sites by the unique layer structure, and the hierarchical pore sizes distribution, as well as the electronic effect between Cu and Ce components. In addition, the catalytic mechanism for the cleavage of C C bonds in β -O-4 model probes has been studied via the controlled oxidative degree of model compounds and the isotope-labeling experiments. Therefore, this work provides a new insight into the efficient utilization of lignin via the rational design of catalysts.
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY
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2020
·Vol. 167
·期 8
·087502
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IF 3.721
Ya Li,Lina Hou,Zhiling Liu,Wenbo Lu,Man Zhao,He Xiao,Tianjun Hu,Zhanfeng Zheng,Jianfeng Jia,Haishun Wu
Mucin 1 protein (MUC1) is a well-known tumor marker overexpressed in a variety of human malignancies, and thus its highly selective and sensitive detection is significantly desired for clinical diagnostics. Herein, a sensitive electrochemical MUC1 sensing platform has been fabricated based on copper-based metal-organic frameworks (Cu-MOFs) decorated with gold-platinum alloy nanoparticles (AuPt NPs). Besides serving as a redox probe to avoid introducing extra redox media, the electroactive Cu-MOFs function as catalysts in the hydrogen peroxide reduction, resulting in electrochemical signal amplification. Meanwhile, AuPt NPs loaded on the Cu-MOFs mimic horseradish peroxidase to promote the reduction of hydrogen peroxide, giving rise to the secondary-amplified electrochemical signal. Moreover, the target MUC1 triggered catalytic hairpin assembly (CHA) further improves the sensitivity of the developed biosensor via the target recycling amplification. The constructed sensing platform displayed a desirable dynamic range between 10 fM and 10 nM in the MUC1 detection, with a sufficiently low limit-of-detection (3.33 fM). The current strategy of utilizing hybrid nanocomposite consisting of MOFs and alloy NPs and enzyme-free CHA provides a promising platform for the detection of biomarkers in the clinical diagnosis with high selectivity and sensitivity.
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CHEMOSPHERE
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2019
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IF 5.108
Yulin Yang,Ying Liu,Xian Fang,Wei Miao,Xiaoyan Chen,Jing Sun,Bing-Jie Ni,Shun Mao
Transition metal and nanocarbon-based composites with high activity and stability draw great attention in electro-Fenton system for organic pollutants removal . In this study, HKUST-1-derived Cu@C nanoparticles embedded within three-dimensional reduced graphene oxide (rGO) network (denoted as 3DG/Cu@C) is synthesized through a simple strategy. The prepared catalyst shows ordered 3D porous carbon structure and Cu@C NPs are uniformly dispersed in the matrix. The 3DG/Cu@C is used as heterogeneous electro-Fenton (hetero-EF) catalyst and shows outstanding performance in various persistent organic pollutants removal. High concentration Rhodamine B (RhB) (40 mg L −1 ) can achieve a complete decolorization within 150 min with 25 mg L −1 3DG/Cu@C catalyst, which is one of the lowest catalyst dosages in hetero-EF for RhB removal. More importantly, the 3DG/Cu@C achieves high RhB mineralization efficiency of 81.5% and exhibits high catalytic performance in a wide pH window from 3 to 9. The 3DG/Cu@C also remains high efficiency after five successive reaction cycles. The working mechanism study shows that RhB is mainly oxidized by • OH and O 2 •- radicals through hetero-EF and anodic oxidation processes. The high stability and outstanding performance of 3DG/Cu@C provide new insights in organic pollutants removal by hetero-EF process with transition metal and nanocarbon-based catalysts.
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高影响因子
SENSORS
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2019
·Vol. 19
·期 22
·5055
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IF 3.031
Min Jiang,Peng Sun,Jie Zhao,Lihua Huo,Guofeng Cui
Flexible physiological medical devices have gradually spread to the lives of people, especially the elderly. Here, a flexible integrated sensor based on Au nanoparticle modified copper hydroxide nanograss arrays on flexible carbon fiber cloth ([email protected](OH)2/CFC) is fabricated by a facile electrochemical method. The sensor possesses ultrahigh sensitivity of 7.35 mA mM−1cm−2in the linear concentration range of 0.10 to 3.30 mM and an ultralow detection limit down to 26.97 nM. The fantastic sensing properties can be ascribed to the collective effect of the superior electrochemical catalytic activity of nanograss arrays with dramatically enhanced electrochemically active surface area as well as mass transfer ability when modified with Au and intimate contact between the active material ([email protected](OH)2) and current collector (CFC), concurrently supplying good conductivity for electron/ion transport during glucose biosensing. Furthermore, the device also exhibits excellent anti-interference and stability for glucose detection. Owing to the distinguished performances, the novel sensor shows extreme reliability for practical glucose testing in human serum and juice samples. Significantly, these unique properties and the soft structure of silk fabric can provide a promising structure design for a flexible micro-device and a great potential material candidate of electrochemical glucose sensor.Keywords:Cu(OH)2nanograss;Au nanoparticles;glucose detection;flexible electrochemical biosensor
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
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2019
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IF 3.571
Yafu Tang,Shanmin Hou,Yuechao Yang,Dongdong Cheng,Bin Gao,Yongshan Wan,Yuncong C. Li,Zhen Yu,Yuanyuan Yao,Jiazhuo Xie
The complex synthesis process, low utilization, and single function of fungicides have seriously hindered the development of fungicides in resistance to rice sheath blight. Here, an inexpensive and multifunctional Cu(II)-based water-dispersible humic acid (Cu-WH) fungicide with growth-promoting ability was developed with a simple method. A 3D molybdate carbon hierarchical nanosphere (MoO2-C-HN) catalyst was successfully synthesized using a green route and applied in a solid-phase activation of lignite to obtain water-dispersible humic acid. Cu(II)-based water-dispersible humic acid (Cu-WH) was then formed through a simple reaction of Cu(II) and the humic acid. The resultant Cu-WH showed strong antifungal performance against Rhizoctonia solani in laboratory incubation experiments. After being treated with Cu3-WH (0.1 mg L–1), the control efficiency of rice sheath blight at 1, 3, and 5 days after infection was 90.54%, 78.96%, and 66.31%, respectively. It also enhanced the water-holding capacity of the substrate and thus effectively improved the growth of rice seedlings. In comparison to commercial rice seedling substrate, the substrate treated with 8 wt % of Cu3-WH increased plant height, stem diameter, fresh weight, and chlorophyll content by 19.23%, 35.91%, 14.52%, and 42.85%, respectively. The newly developed Cu-WH thus can be used as a novel low-cost efficient fungicide and growth stimulator to treat rice sheath blight as well as to increase rice production.
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OPTICAL MATERIALS
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2019
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IF 2.687
Jing Fang,Shujuan Zhuo,Changqing Zhu
In this study, we presented a facile strategy to synthesis Cu-doped carbon dots (Cu-CDs) through one-step hydrothermal approach using CuCl 2 ·2H 2 O and ethanediamine as reaction precursor. Interestingly, the fluorescence of Cu-CDs can be quenched greatly in the presence of p -nitrophenol. Thus, a high selectivity and sensitivity fluorescent sensing platform is constructed for the detection of p -nitrophenol on account of the inner filter effect . Under the optimal condition, the linear detection range is 0.5–50 μM with the detection limit of 0.08 μM (S/N = 3). This method is successfully applied in quantification of p -nitrophenol in lake water samples, which exhibits potential application prospect.
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CHEMICAL ENGINEERING JOURNAL
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2019
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IF 8.355
Xiaoqiang Wang,Yue Liu,Zhongbiao Wu
In this paper, the Cu-Ce based catalyst using NbOPO 4 (Nb-P) as support was firstly employed for selective catalytic reduction (SCR) of NO by NH 3 . The experimental results had illustrated that such catalyst exhibited well SCR activity and N 2 selectivity within a wide temperature range of 200–450 °C. These superior performances could be mainly attributed to its improved textural properties and strong acidity derived from NbOPO 4 support. More importantly, the sulfur tolerance of the NbOPO 4 supported Cu-Ce sample was found greatly improved compared to TiO 2 and Ti-Nb supported samples, where above 80% SCR activity of Cu-Ce/Nb-P sample was obtained at 250 °C after 10 h reaction running in the presence of 100 ppm SO 2 . This fact was the result of the enhanced acidity and the strong interactions between Cu-Ce oxides and NbOPO 4 support, which could prevent the surface oxygen species from sulfation by SO 2 . As such, these oxygen species strongly associated with NbOPO 4 support still could activate adsorbed NH 3 to fulfill the SCR reaction cycle, leading to its better sulfur resistance. The work would provide some enlightenments to the development of NH 3 -SCR catalysts with high sulfur resistance at medium-high temperature.
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CHEMICAL ENGINEERING JOURNAL
·
2022
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IF 16.744
Yang Peng,Zhanwei Xu,Le Yu,Xucheng Li,Weiran Yang
The direct conversion of furfural (FUR) to 2-methyltetrahydrofuran (2-MTHF) was investigated over a trimetallic CuNiRe/Hβ catalyst. Under optimal reaction conditions at 240 °C under 3 MPa H 2 for 1 h, almost complete conversion of FUR and high-yield of 2-MTHF (81 %) was achieved. This is the highest yield reported for the direct conversion of FUR to 2-MTHF. HR-TEM demonstrated that the growth of Cu nanoparticles (NPs) on the surface of Hβ was inhibited after loading Ni or Re resulted in the smaller Cu particle size and better hydrogenation and hydrodeoxygenation activity. H 2 -TPR characterization exhibited that the reducibility of bimetallic and trimetallic catalysts was higher than that of monometallic catalysts·NH 3 -TPD explained that Hβ acid sites mainly contributed to FUR deoxygenation. The adsorption configurations of FUR, furfuryl alcohol (FOL) and 2-methylfuran (2-MF) on the catalyst were revealed by ATR-IR. Catalyst evaluation and control experiments proved that FUR was first hydrogenated to FOL, followed by hydrodeoxygenation to 2-MF, and finally hydrogenated to 2-MTHF catalyzed by the combination of three metals.
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CHEMICAL ENGINEERING JOURNAL
·
2022
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IF 16.744
Xiaoping Liu,Yunbo Zhai,Zhixiang Xu,Liming Liu,Wanying Ren,Yu Xie,Caiting Li,Yun Zhu,Min Xu
The high water content of sewage sludge increases the processing costs and hampers its further disposal. Fenton technology has proven to be efficient and been widely used to enhance sludge dewaterability, but it usually needs acidification and subsequent neutralization, thus consuming a lot of chemicals. It’s well documented that hydroxyl radicals produced in various Fenton or Fenton-like reactions play a crucial role in sludge dewatering. Based on the latest study, Cu + and Cu + /H 2 O 2 pretreatments for the enhanced dewaterability of sludge without extra pH adjustment were proposed. Results showed that Cu + with and without H 2 O 2 can significantly improve the dewatering performance of sludge, which was ascertained by a capillary suction time (CST) reduction rate of about 80 %. The proteins and polysaccharides in tightly-bound extracellular polymeric substance (TB-EPS) were decreased, while increased in soluble extracellular polymeric substance (S-EPS). In addition, a hydrophobic and porous surface was formed, and zeta potential increased after conditioned. These changes may release bound water and thus improve sludge dewaterability. The results of electron spin resonance and scavenging tests signaled that the Cu 3+ was mainly accountable for the dissolution of EPS, rather than the hydroxyl radicals ( OH). Our results substantiate and untangle a distinct reinforcement mechanisms for sludge dewatering by high valent copper (Cu 3+ ). This study demonstrates for the first time that Cu 3+ plays an important role in sludge dewatering, which has long been credited to hydroxyl radicals. It also urges re-evaluation of the Fenton(-like) system for sludge dewatering, given that Cu 3+ could also cause potential oxidative destruction of EPS compared with reactive oxygen species.
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