JOURNAL OF COLLOID AND INTERFACE SCIENCE
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2020
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IF 7.489
Huanfang Zhou,Limin Chen,Shuting Li,Songqing Huang,Yingying Sun,Yanhong Chen,Zhao Wang,Wei Liu,Xinchun Li
A facile and green method for preparation of gold/palladium (Au/Pd) bimetallic nanoparticles interleaved reduced graphene oxide (rGO) composite was presented. One-step electroreduction of Au/Pd precursors and graphene oxide synergistically produced a multilayered and well-structured nanohybrid on glassy carbon electrode, which was explored as a highly efficient electrocatalyst . This operation is easy and controllable, as compared with time-consuming and procedure-tedious hydrothermal synthesis . The morphology and chemical constituents were meticulously characterized. The remarkable electrocatalytic performance of the prepared nanohybrid was demonstrated by detection of a high-risk carcinogen pollutant, hydrazine. By optimizing the preparation condition and investigating the electrochemical behavior, we achieved the sensitive analysis of hydrazine with ultralow oxidation overpotential. Amperometry was employed for constructing the quantitative calibration curve ; the steady-state current originating from hydrazine oxidation was proportional to the analytical concentration ranging from 0.1 μM to 200 μM, with the detection limit of 16 nM. Moreover, the nanohybrid displayed considerable anti-interfering ability with respect to hydrazine detection, as a variety of potentially coexisting substances produced negligible electrochemical response in the given analytical condition. Advantages including easy-to-preparation, high sensitivity and favorable selectivity , as well as broad linear response make the present method feasible for monitoring of hydrazine in water environment.
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高影响因子
NEW JOURNAL OF CHEMISTRY
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2020
·Vol. 44
·期 7
·2890-2896
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IF 3.288
Yinhui Yang,Meiling Qi,Jinliang Wang
Here we report a novel hexaphenylbenzene (HPB)-based material functionalized with six tetraphenylethylene units (BPT) with unique conformation-driven selectivity for gas chromatographic (GC) separations. It is composed of a neat aromatic hydrocarbon with a rigid propeller-like conformation. As a result, the BPT capillary column exhibited high column efficiency of 5340 plates per m and high-resolution capability for aromatic to aliphatic isomers with excellent intra-day and inter-day repeatability and between-column reproducibility. The results demonstrate the unique conformation-driven selectivity of the HPB-based stationary phase, which is rarely reported for chromatography. Moreover, its application in the determination of isomer impurities in commercial products proved its good potential for practical GC analysis. This work presents a new perspective for developing selective stationary phases by engineering their structures.
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JOURNAL OF CHROMATOGRAPHY A
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2020
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IF 4.049
Luping Sun,Shuyun Zhu,Zhenjia Zheng,Jing Sun,Xian-En Zhao,Huwei Liu
Hydroxyl-polycyclic aromatic hydrocarbons (OH-PAHs) are biomarkers for assessing the exposure levels of polycyclic aromatic hydrocarbons (PAHs). A series of stable isotope mass tags (SIMT-332/338/346/349/351/354/360/363/374/377) were firstly designed and synthesized to perform multiplexed stable isotope labeling derivatization (MSILD) of OH-PAHs in human plasma and urine. Their derivatives were enriched and purified by magnetic dispersive solid phase extraction (MDSPE) using prepared Fe 3 O 4 /GO and then determined by ultra high performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) in multiple reaction monitoring mode. 9-Plexed MSILD reagents were prepared using pipemidic acid as core structure with different isotope mass tags, in which carbonyl chloride group was used to label OH-PAHs. The SIMT-346 labeled OH-PAHs standards were used as internal standards, which can greatly increase the quantitative accuracy. 9-Plex labeled nine different real samples can be quantified by UHPLC-MS/MS in a single run. Under optimized MSILD-MDSPE conditions, good linearities of seven OH-PAHs were obtained with satisfactory coefficient of determination R 2 > 0.991. Limits of detection (LODs) of seven OH-PAHs were from 0.1 to 0.5 pg/mL, and limits of quantitation (LOQs) ranged from 0.5 to 2.0 pg/mL. The intra- and inter-day precisions ranged in 2.3–12.4% with accuracies in the range of 91.7–108.4%. Acceptable results of matrix effect (89.7–105.7%) and derivatization efficiency (> 96.4%) were obtained. In short, the developed method has been proved to be high-throughput, sensitive, accurate and easy-handling. This method was applied for the measurement of seven free OH-PAHs in human urine and plasma, and expected to provide technical support for the evaluation of PAHs exposure levels in humans.
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CONSTRUCTION AND BUILDING MATERIALS
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2019
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IF 4.046
Jianfeng Ma,Yazhuo Shang,Changjun Peng,Honglai Liu,Shuzhen Zheng,Hongxia Zhao,Shuai Qi,Qianping Ran
Air content can greatly affect the properties of concrete, therefore, the development of high efficient air-entraining agents is important. In this work, novel phosphate-modified polymers with different aryl substitutions were synthesized and used as highly efficient air-entraining agents. The structure of polymers was characterized by 1 H NMR and IR spectra. The foamability and foam stability of the different polymeric surfactants were tested in solutions. Surfactants with large steric hindrance, such as APP-6, showed superior performance of foamability and foam stability. In view of the excellent foamability properties of synthesized polymers in aqueous solution, the application of these polymers used in cement mortar as air-entraining agents were also evaluated for practical application. The surface tension, theoretical calculation and dynamic light scattering test for these polymeric surfactants were also studied. The synthetic aryl-polyether-phosphate surfactants showed higher surface activity, foamability, foam stability, and air-entraining performance compared with commercial air-entraining agent.
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SCIENCE OF THE TOTAL ENVIRONMENT
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2019
·
IF 5.589
Shanshan Sun,Haizhen Wang,Binxin Fu,Hao Zhang,Jun Lou,Laosheng Wu,Jianming Xu
Rhodococcus sp. WB9, a strain isolated from polycyclic aromatic hydrocarbons contaminated soil, degraded phenanthrene (PHE, 100 mg L −1 ) completely within 4 days. 18 metabolites were identified during PHE degradation, including 5 different hydroxyphenanthrene compounds resulted from multiple routes of initial monooxygenase attack. Initial dioxygenation dominantly occurred on 3,4-C positions, followed by meta -cleavage to form 1-hydroxy-2-naphthoic acid (1H2N). More than 95.2% of 1H2N was transported to and kept in extracellular solution without further degradation. However, intracellular 1H2N was converted to 1,2-naphthalenediol that was branched to produce salicylate and phthalate. Furthermore, 131 genes in strain WB9 genome were related to aromatic hydrocarbons catabolism, including the gene coding for salicylate 1-monooxygenase that catalyzed the oxidation of 1H2N to 1,2-naphthalenediol, and complete gene sets for the transformation of salicylate and phthalate toward tricarboxylic acid (TCA) cycle. Metabolic and genomic analyses reveal that strain WB9 has the ability to metabolize intracellular 1H2N to TCA cycle intermediates, but the extracellular 1H2N can’t enter the cells, restricting 1H2N bioavailability and PHE mineralization.
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CHEMICAL ENGINEERING JOURNAL
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2019
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IF 8.355
Yizhou Tu,Guizhou Xu,Lu Jiang,Xuejiao Hu,Jun Xu,Xianchuan Xie,Aimin Li
Amphiphilic hyper-crosslinked porous cyclodextrin polymer (PBCD-B-D) with a surface area of 1445 m 2 g −1 was synthesized for rapid removal of organic micropollutants. Partially benzylated cyclodextrin was crosslinked with 4,4′-bis(chloromethyl)-1,1′-biphenyl and α,α'-dichloro-p-xylene by the Friedel–Crafts alkylation reaction. The hydrophilicity of the PBCD-B-D surface is modulated by controlling the number of hydroxyl groups on cyclodextrin. Benzylation reaction is more likely to occur at the C-2 and C-6 positions of cyclodextrin hydroxyl groups according to Gaussian computation. Four different water-soluble pollutants (3-phenylphenol, 2-naphthol, p-nitrophenol, and 4-chlorophenol) were selected for adsorption study. The adsorption rate of PBCD-B-D is extremely high, and the removal efficiency reaches above 95% in 1 min. For the adsorption of 3-phenylphenol and 2-naphthol, the rate constants of PBCD-B-D are 827–1187 and 396–413 times larger than those of granular activated carbon (GAC) and β-cyclodextrin polymer crosslinked with epichlorohydrin (EPI-CDP), respectively. The adsorption capacity of PBCD-B-D is 2 and 4 times higher than that of GAC and EPI-CDP, respectively. The combination of cyclodextrin inclusion mechanism, hydrophobic attraction, and hydrogen bonding allows PBCD-B-D to adsorb both hydrophobic and hydrophilic pollutants. PBCD-B-D can be easily regenerated at room temperature using methanol as eluent. In addition, PBCD-B-D showed excellent adsorption performance towards mixed pollutants at environmentally relevant concentrations. According to the thermodynamic study, the adsorption of organic compounds onto PBCD-B-D belongs to physical adsorption and is spontaneous. PBCD-B-D is a potential novel adsorbent for water treatment owing to its excellent adsorption performance, low cost, and good regenerability.
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JOURNAL OF CHROMATOGRAPHY A
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2023
·
IF 4.1
Kai Hu,Tiantian Pang,Cheng Yang,Pengzhao Han,Lixin Li,Pan Wang,Zhenqiang Zhang,Wenjie Zhao,Shusheng Zhang
Urinary hydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) and catecholamines (CAs) are important biomarkers of PAHs exposure. In this study, a novel magnetic boronic acid hypercrosslinked composite (Fe 3 O 4 @HCP-BA) is synthesized using a facile one-pot strategy and applied as a sorbent for the simultaneous extraction of OH-PAHs and CAs in urine samples. The synthesized Fe 3 O 4 @HCP-BA composites are characterized by rich pore structure, highly specific surface area, good magnetic response, and excellent selectivity and adsorption efficiency (range: 65.26–496.71 and 1227.3–1581.8 µmol g −1 for CAs and OH-PAHs, respectively). The mechanisms governing the adsorption of the OH-PAHs and CAs to the Fe 3 O 4 @HCP-BA composites were systematically studied via adsorption kinetics, isotherm models, XPS characterization, and molecular simulation. The resultant Fe 3 O 4 @HCP-BA composite-based MSPE/HPLC-FLD method exhibited good linearity (R 2 > 0.9916), low limits of detection (0.2–0.3 pg mL −1 and 0.2–0.3 ng mL −1 for OH-PAHs and CAs, respectively), and good precision (intra-day and inter-day RSDs < 11.1%). The analysis of CAs and OH-PAHs in the urine samples from 14 smokers and 14 non-smokers revealed a positive correlation between the concentrations of CAs and OH-PAHs. Our findings not only establish the proposed method as a green, environmentally friendly, and simple strategy for preparing magnetic adsorbents, but also confirm it as a promising alternative method for accurate determination of OH-PAHs and CAs in biological samples.
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JOURNAL OF CHROMATOGRAPHY A
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2023
·
IF 4.1
Chun-Ying Xu,Yuan-Yuan Cui,Cheng-Xiong Yang
Endocrine disrupting chemicals (EDCs) are a typical class of natural or man-made endogenous hormone agonists or antagonists that can directly or potentially interfere with human endocrine system. However, it is still difficult to analyze trace EDCs directly from complex environment and food matrices. Therefore, the proper sample pretreatment is highly desired and the preparation of efficient adsorbents is of great challenge and importance. Herein, we report the facile one-pot solvothermal synthesis of Fe 3 O 4 nanoparticle doped magnetic β-cyclodextrin microporous organic network composites (MCD-MONs) for the magnetic solid phase extraction (MSPE) of four phenolic EDCs in water and food takeaway boxes prior to the high-performance liquid chromatography analysis. The sheet-like Fe 3 O 4 doped MCD-MONs offered good magnetic property (16.5 emu g −1 ) and stability, and provided numerous hydrogen bonding, hydrophobic, π-π, and host-guest interaction sites for EDCs. Under the optimal experimental conditions, the established method was successfully verified with wide linear range (2.0–1000 µg L −1 ), low limits of detection (0.6–1.0 µg L −1 ), good precisions (intra-day and inter-day RSDs < 5.2 %, n = 3), large enrichment factors (88–98) and adsorption capacity (90.3–255.8 mg g −1 ), short extraction time (6 min), less adsorbent consumption (3 mg), and good reusability (at least 8 times) for EDCs. The proposed method was successfully applied to detect the trace EDCs in real samples with the recovery of 84.0–99.7 %. This work demonstrated the great potential of MCD-MONs for the efficient MSPE of trace EDCs from complex food takeaway boxes and water samples and uncovered the prospect of CD-based MONs in sample pretreatment.
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CHEMICAL SOCIETY REVIEWS
·
2023
·Vol. 52
·期 17
·6031-6074
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IF 46.2
Ziming Zhao,Xianghui Liu,Mengqi Zhang,Leyuan Zhang,Changkun Zhang,Xianfeng Li,Guihua Yu
Realizing decarbonization and sustainable energy supply by the integration of variable renewable energies has become an important direction for energy development. Flow batteries (FBs) are currently one of the most promising technologies for large-scale energy storage. This review aims to provide a comprehensive analysis of the state-of-the-art progress in FBs from the new perspectives of technological and environmental sustainability, thus guiding the future development of FB technologies. More importantly, we evaluate the current situation and future development of key materials with key aspects of green economy and decarbonization to promote sustainable development and improve the novel energy framework. Finally, we present an analysis of the current challenges and prospects on how to effectively construct low-carbon and sustainable FB materials in the future.
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CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Han Zhang,Wen Sun,Lida Wang,Shiheng Ma,Wenxiang Xing,Kun Liang,Guichang Liu
The intrinsic repair ability is a new strategy to prolong the protection life of damaged coatings, but how to maintain long-term corrosion protection during repeated healing remains a challenge. Herein, a self-healing, weather-resistant polyurethane coating with long-term stable corrosion protection enhanced by dopamine-coated graphene oxide (GP) fillers was developed. The formation of hydrogen bond between GP and the amino group in the polyurethane chain enhances the interfacial compatibility of the filler in the coating, thus improves the photothermal, thermal conductivity and barrier properties of the coating. The coating maintains excellent corrosion protection properties after 7 times of scratch-healing cycles, and can withstand up to 15 days of immersion after scratch-healing. The water evaporation rate and deicing rate of the coating are respectively up to 5.57 and 4965.5 kg/(m 2 ·h), achieving a highly photothermal conversion efficiency. In addition, molecular dynamics simulation demonstrates that the hydrogen bonds between GP and polyurethane chains is the key factor for the excellent corrosion protection of the coating. This study opens a new avenue for improving the service life of self-healing coatings in atmospheric environment.
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ACS Sustainable Chemistry & Engineering
·
2023
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IF 8.4
Cong Chang,Shenghai Yang,Shanshan Liu,Henghui Wang,Hong Liu,Junjie Qu,Wei Jin,Changhong Wang,Yongming Chen
As the mainstream hydrometallurgical medium of bismuth sulfide concentrate, chloride/hydrochloric acid suffers from high volatility, strong corrosiveness, and inferior deposit quality. In this paper, methanesulfonic acid (MSA) with low volatility and high stability was adopted as the bismuth hydrometallurgical system, and the membrane electrochemical deposition method was proposed to extract bismuth metal from a bismuth-containing solution. The effects of additives, such as calcium lignosulfonate (CL), tetrabutylammonium chloride, β-naphthol, and lugalvan NES, on the morphology of bismuth deposits and electric energy consumption (EEC) were investigated in detail. The addition of CL as an additive could produce dense and flat bismuth deposits while the EEC is reduced simultaneously. Cyclic voltammetry and chronoamperometry analysis reveal the electrochemical behavior of bismuth deposition in the CL-assisted MSA medium, and the nucleation and growth of bismuth grains follow a 3D ″nucleation/growth″ mechanism. Under a cathode current density of 180 A/m2, a flat metallic bismuth deposit (purity > 99.96%) is produced in the presence of 0.5 g/L CL. The cathodic current efficiency (CCE) and EEC of membrane electrodeposition are 98.25% and 705 kWh/t Bi, respectively. Compared with chloride/hydrochloric acid, the bismuth membrane electrodeposition process in the CL-assisted MSA system has the advantages of being energy-saving, green, and safe, and it has a good application prospect in the field of bismuth hydrometallurgy.
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Canadian Journal of Chemistry
·
2019
·Vol. 97
·期 4
·
IF 1.252
Jun Wang,Junyi Xie,Libo Wang,Yan Jiang,Na Zhang
A salen nickel complex has been prepared in good yield with ethylenediamine, salicylaldehyde, and NiCl2·6H2O as raw materials. The structure of the complex was characterized by FTIR, 1H NMR, UV, and ESI-MS. Upon activation with methylaluminoxane (MAO), the precatalyst showed high activity for ethylene oligomerization. To reduce the simultaneous production of insoluble polymers during the nickel-catalyzed ethylene oligomerization, a series of phenolic compounds were introduced as modifiers for the production of linear α-olefins. The researched result showed that the phenolic compounds have a significant impact on the selectivity of oligomers and the concentration of polymers. With the increase of phenolic compounds, the content of polymers decreased and the distribution of oligomers gradually shifted toward lighter olefins. The sterically hindered 4-tert-butyphenol proved to be an especially efficient polymer-retarding modifier among the studied phenolic compounds in this work. Furthermore, the retarding effect of phenolic compounds toward insoluble polymers may be mainly related to their interaction with MAO, giving rise to larger MAO aggregates.
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危险品化学品经营许可证（带存储）