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排序方式: 共有1141条查询结果,搜索用时 15 毫秒
41.
《Arabian Journal of Chemistry》2022,15(4):103747
Al2O3/chitosan-multiwall carbon nanotubes (MWCNTs) were created to increase the exchange capacity of polyvinylidene fluoride (PVDF) ion-exchange membranes. The composite membranes were made by mixing Al2O3 nanoparticles into the PVDF cast solution, then applying a thin coating of chitosan functionalized carbon nano tubes (Cs-MWCNTs) to the PVDF membrane surface. The structure and characteristics of the hybrid membranes were described using XRD, SEM, IR, and TG-DTA. The Al2O3-PVDF/Cs-MWCNTs membrane beat the other Al2O3-PVDF/Cs, Al2O3-PVDF, and PVDF membranes in terms of molybdate, phosphate, and nitrate adsorption. The removal efficiency, pH solution, adsorption capacity, and desorption process of molybdate, phosphate, and nitrate anions by Al2O3-PVDF and PVDF membranes were investigated. The removal effectiveness of molybdate, phosphate, and nitrate, according to the testing findings, was 94.3, 65.6, and 85.78 %, respectively. The adsorption of MoO42?, PO43?, and NO3? increased as the pH increased initially until the best adsorption was achieved, and then decreased significantly as the pH increased further. The total adsorption capabilities of MoO42?, PO43?, and NO3?for the Al2O3-PVDF/Cs-MWCNTs membrane were 65.50, 61.22, and 59.77 mg/g, respectively. Using regeneration and reuse experiments for the simultaneous adsorption of molybdate, phosphate, and nitrate during three consecutive cycles, the adsorption/desorption of Al2O3-PVDF/Cs-MWCNTs was assessed. Al2O3-PVDF/Cs-MWCNTs offer a lot of promise when it comes to eliminating MoO42?, PO43?, and NO3?from actual wastewater samples. 相似文献
42.
《Arabian Journal of Chemistry》2022,15(7):103925
A cost-efficient kaolinite-cellulose/cobalt oxide green nanocomposite (Kao-Cel/Co3O4 NC) was successfully synthesized, and utilized as a promising material for removing Pb2+ and Cd2+ from aqueous solution. The fabricated nanocomposite has been characterized by Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy-energy dispersive X-ray, high-resolution transmission electron microscopy, and Brunauer-Emmett-Teller analysis. The batch methodology was exploited for optimization of process parameters and the optimized conditions were found to be adsorbent dosage (2.0 g/L), extraction time (50 min), initial concentration (60 mg/L), and initial solution pH (6). Kao-Cel/Co3O4 NC displayed excellent adsorption properties and achieved maximum saturation capacity (Qm) of 293.68 mg Pb2+/g and 267.85 mg Cd2+/g, with an equilibration time of 50 min at 323 K. The Langmuir model best expressed the isotherm data recommending the adsorption onto energetically homogeneous NC surface, while the compatibility of kinetics data with pseudo-second-order model revealed the dependency of adsorption rate on adsorption capacity, and probable involvement of chemisorption in the rate-controlling step. Electrostatic interaction and ion exchange mechanism were responsible for the uptake of Pb2+ and Cd2+ by Kao-Cel/Co3O4 NC as demonstrated by Fourier transform infrared spectroscopy and pH studies. Thermodynamic parameters confirmed the physical, spontaneous, and endothermic sequestration processes. Real water investigation specified that the present adsorbent could be effectively used for liquid phase decontamination of Pb2+ and Cd2+. The nanocomposite exhibited high reusability, which could be utilized efficiently for five runs with sustainable results. In summary, this study portrayed the present nanocomposite as an emerging material for the adsorption of heavy metal ions particularly Pb2+ and Cd2+. 相似文献
43.
《Arabian Journal of Chemistry》2022,15(12):104261
Nowadays, sustainable supplement of water has recently been identified as a vital necessity due to the existence of limited drinkable water sources. To do this, various techniques are being developed to remove various types of pollutants from water/wastewater sources. Adsorption of common water pollutants using nanocomposite materials has been of great popularity in recent years due to its high efficiency. This paper aims to develop various models based on machine learning approach to study their efficiency on predicting the experimentally measured results of Hg/Ni ions removal from water sources. To do this, this study attempts regression on a small data set using two parameters as inputs and two parameters as outputs. In this dataset, the inputs are Ion and C0, and the outputs are Ce and Qe. AdaBoost (Adaptive Boosting), a well-known ensemble method, was applied on top of three different models, including Decision Tree Regression (DT), Gaussian Process Regression (GPR), and Linear Regression (LR). After fine-tuning their hyper-parameters, the optimized model was evaluated through various metrics. For example, the R2 for ADA + GPR model has a score of 0.998 for Ce and 0.999 for Qe as the best model among these three models. This model in RMSE is the best and illustrates 0.1512 and 1.490 for Ce and Qe as error. Eventually, ADA + GPR has been selected as the optimized model with optimized dataset: (Ion = Ni, C0 = 250, Ce = 206.0). But for Qe, different amounts are illustrated: (Ion = Hg, C0 = 106.7, Ce = 577.35) 相似文献
44.
San-E Zhu Jian-Hui Zhang Yu Gong Li-Feng Dou Li-Hua Mao Hong-Dian Lu Chun-Xiang Wei Hong Chen Xue-Fei Wang Wei Yang 《Molecules (Basel, Switzerland)》2021,26(5)
A broadband visible light-absorbing [70]fullerene-BODIPY-triphenylamine triad (C70-B-T) has been synthesized and applied as a heavy atom-free organic triplet photosensitizer for photooxidation. By attaching two triphenylmethyl amine units (TPAs) to the π-core of BODIPY via ethynyl linkers, the absorption range of the antenna is extended to 700 nm with a peak at 600 nm. Thus, the absorption spectrum of C70-B-T almost covers the entire UV–visible region (270–700 nm). The photophysical processes are investigated by means of steady-state and transient spectroscopies. Upon photoexcitation at 339 nm, an efficient energy transfer (ET) from TPA to BODIPY occurs both in C70-B-T and B-T, resulting in the appearance of the BODIPY emission at 664 nm. Direct or indirect (via ET) excitation of the BODIPY-part of C70-B-T is followed by photoinduced ET from the antenna to C70, thus the singlet excited state of C70 (1C70*) is populated. Subsequently, the triplet excited state of C70 (3C70*) is produced via the intrinsic intersystem crossing of C70. The photooxidation ability of C70-B-T was studied using 1,5-dihydroxy naphthalene (DHN) as a chemical sensor. The photooxidation efficiency of C70-B-T is higher than that of the individual components of C70-1 and B-T, and even higher than that of methylene blue (MB). The photooxidation rate constant of C70-B-T is 1.47 and 1.51 times as that of C70-1 and MB, respectively. The results indicate that the C70-antenna systems can be used as another structure motif for a heavy atom-free organic triplet photosensitizer. 相似文献
45.
《中国化学快报》2021,32(11):3509-3513
At present, frequent outbreaks of bacteria and viruses have seriously affected people's normal lives. Therefore, the study of broad-spectrum antibacterial nanocomposites is very promising. However, most antibacterial materials have some disadvantages, such as single bactericidal mechanisms and unrepeatable use. Based on the current situation, a kind of nanocomposite with three structures of graphene oxide (GO), quaternary ammonium salt (QAs) and N-halamine was prepared, which showed synergistic effect to improve antibacterial activity and combined with a variety of sterilization mechanisms. Meanwhile, GO can provide richer ways of sterilization and high specific surface area, which is conducive to the grafting of quaternarized N-halamine. The advantages of physical sterilization of GO, charge adsorption of QAs, reuse of N-halamine and efficient sterilization are fully utilized. The results showed that the quaternarized N-halamine-grafted GO was obtained successfully. GO grafted with quaternarized N-halamine polymer showed strong speedy bactericidal activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) (99%). It had good storage and regeneration properties. 相似文献
46.
Eman M. Moaaz Amr M. Mahmoud Ahmed S. Fayed Mamdouh R. Rezk Ezzat M. Abdel-Moety 《Electroanalysis》2021,33(8):1895-1901
Antibiotics determination plays a major role in minimizing antimicrobial resistance starting from quality control of pharmaceutical formulations to therapeutic drug monitoring. Green modified glassy carbon electrode has been developed for determination of tedizolid phosphate; new antibiotic prodrug; in presence of its active metabolite. The graphene transducer interlayer, dispersed with PVC, improved the electrode stability and standard potential reproducibility. Graphene hydrophobicity prevented the water layer formation between the sensing layers that decreased the potential drift down to 267 μV h−1. Electrochemical impedance showed a low resistance value for graphene containing sensor due to its high electron transfer ability. 相似文献
47.
Alexander K. Mengele Dominik Weixler Avinash Chettri Maite Maurer Fabian Lukas Huber Prof. Gerd M. Seibold Prof. Benjamin Dietzek Prof. Bernhard J. Eikmanns Prof. Sven Rau 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(68):16840-16845
A series of three Ru(II) polypyridine complexes was investigated for the selective photocatalytic oxidation of NAD(P)H to NAD(P)+ in water. A combination of (time-resolved) spectroscopic studies and photocatalysis experiments revealed that ligand design can be used to control the mechanism of the photooxidation: For prototypical Ru(II) complexes a 1O2 pathway was found. Rudppz ([(tbbpy)2Ru(dppz)]Cl2, tbbpy=4,4'-di-tert-butyl-2,2'-bipyridine, dppz=dipyrido[3,2-a:2′,3′-c]phenazine), instead, initiated the cofactor oxidation by electron transfer from NAD(P)H enabled by supramolecular binding between substrate and catalyst. Expulsion of the photoproduct NAD(P)+ from the supramolecular binding site in Rudppz allowed very efficient turnover. Therefore, Rudppz permits repetitive selective assembly and oxidative conversion of reduced naturally occurring nicotinamides by recognizing the redox state of the cofactor under formation of H2O2 as additional product. This photocatalytic process can fuel discontinuous photobiocatalysis. 相似文献
48.
Self-assembled lamellar nanochannels in polyoxometalate-polymer nanocomposites for proton conduction
Haibo He Gang Wang Shengchao Chai Xiang Li Liang Zhai Lixin Wu Haolong Li 《中国化学快报》2021,32(6):2013-2016
The construction of nanostructured ion-transport channels is highly desirable in the design of advanced electrolyte materials,as it can enhance ion conductivity by offering short ion-transport pathways.In this work,we present a supramolecular strategy to fabricate a nanocomposite electrolyte containing highly ordered lamellar proton-conducting nanochannels,by the electrostatic self-assembly of a polyoxometalate H_3 PW_(12)O_(4 O)(PW) and a comb copolymer poly(4-methlstyrene)-graft-poly(N-vinyl pyrrolidone).PW can effectively regulate the self-assembling order of polymer moieties to form a large-ra nge lamellar structure,meanwhile,introducing protons into the nanoscale lamellar domains to build proton transport channels.Moreover,the rigid PW clusters contribute a remarkable mechanical reinforcement to the nanocomposites.The lamellar nanocomposite exhibits a conductivity of 4.3 × 10~(-4) S/cm and a storage modulus of 1.1 × 10~7 Pa at room temperature.This study provides a new strategy to construct nanostructured ion-conductive pathways in electrolyte materials. 相似文献
49.
Metal-oxide nanocomposites were prepared over screen-printed gold electrodes to be used as room-temperature NOx (nitric-oxide (NO) and nitrogen dioxide (NO2)) sensors. Various weight ratios of SnO2–WO3 and Pt loadings were used for NO sensing. The sensing materials were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM) and BET surface analysis. The NO-sensing results indicated that SnO2–WO3 (1:2) was more effective than other materials were. The sensor response (S=resistance of N2/resistance of NO=RN2/RNO) for detecting 1000 ppm of NO at room temperature was 2.6. The response time (T90) and recovery time (TR90) was 40 s and 86 s, respectively. By further loading with 0.5% Pt, the sensor response increased to 3.3. The response and recovery times of 0.5% Pt/SnO2–WO3 (1:2) were 40 s and 206 s, respectively. The linearity of the sensor response for a NO concentration range of 10–1000 ppm was 0.9729. A mechanism involving Pt promotion of the SnO2–WO3 heterojunction was proposed for NO adsorption, surface reaction, and adsorbed NO2 desorption. 相似文献
50.
Visible‐Light‐Mediated Addition of α‐Aminoalkyl Radicals to [60]Fullerene by Using Photoredox Catalysts
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Dr. Yoshihiro Miyake Yuya Ashida Dr. Kazunari Nakajima Prof. Dr. Yoshiaki Nishibayashi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(20):6120-6125
The functionalization of fullerene has been extensively studied and various fullerene derivatives have been synthesized. We have succeeded in the functionalization of [60]fullerene by using α‐aminoalkyl radicals generated by visible‐light‐mediated single‐electron oxidation of α‐silylamines as synthetic intermediates. In these reactions, the introduction of diarylamino groups, which are useful electron donors, has been easily achieved. 相似文献