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2022 ◽  
Vol 204 ◽  
pp. 112070
Author(s):  
J. Aravind Kumar ◽  
T. Krithiga ◽  
G. Narendrakumar ◽  
P. Prakash ◽  
K. Balasankar ◽  
...  

2022 ◽  
Author(s):  
Changjin Jiang ◽  
Ting Zhang ◽  
Shuhui Li ◽  
Zhaoguang Yang

Abstract Fe(III)-chitosan and Fe(III)-chitosan-CTAB composites were prepared using an ionotropic gelation method. Various techniques were used to analyze the morphology, structure, and property of the adsorbents, including SEM, EDS, FT-IR, XPS, and zeta potential. Compared with Fe(III)-chitosan, Fe(III)-chitosan-CTAB was more effective for As(V) adsorption at a wide range of pH (3–8). The adsorption of As(V) onto Fe(III)-chitosan and Fe(III)-chitosan-CTAB could reach equilibrium in 20 min, and their maximum adsorption capacities were 33.85 and 31.69 mg g‒1, respectively. The adsorption kinetics was best described by the pseudo-second-order model (R2=0.998 and 0.992), whereas the adsorption isotherms was fitted well by the Freundlich model (R2=0.963 and 0.987). The presence of H2PO4− significantly inhibited the adsorption of As(V) onto Fe(III)-chitosan and Fe(III)-chitosan-CTAB, and humic acid also led to a slight decrease in As(V) adsorption by Fe(III)-chitosan-CTAB. Over 94% of As(V) at the initial concentration of no more than 5 mg L−1 was removed from real water by the two adsorbents. 1% (w/v) NaOH solution was determined to be the most suitable desorption agent. Fe(III)-chitosan and Fe(III)-chitosan-CTAB still maintained their initial adsorption capacities after five adsorption-desorption cycles. Based on different characterization results, both electrostatic attraction and surface complexation mechanisms played important roles in As(V) adsorption on Fe(III)-chitosan and Fe(III)-chitosan-CTAB.


2022 ◽  
Vol 16 ◽  
Author(s):  
Mustapha Dib ◽  
Marieme Kacem ◽  
Soumaya Talbi ◽  
Hajiba Ouchetto ◽  
Khadija Ouchetto ◽  
...  

Background: Pyran is an heterocyclic oxygen-containing compound that displays a wide range of therapeutic activities. Additionally, pyran is also one of the important structural subunits widely found in pharmaceuticals products. This makes it a recent focus for researchers from the industry and academic institutions. Herein, we reported an efficient and environmentally friendly one-pot strategy for the synthesis of bioactive 4H-pyran compounds via a multicomponent reaction of ethyl acetoacetate, malononitrile and substituted aromatic aldehydes in the presence of the heterogeneous spinel catalyst ( MgAl2O4 ) under mild conditions (room temperature and green solvents). The MgAl2O4 nanocatalyst was prepared from Mg/Al-LDH with a molar ratio 3 of Mg2+/Al3+ by heat treatment at 800°C. The samples were studied by a various characterization techniques such as XRD, TG-dTG, FT-IR and N2 adsorption-desorption. Good to excellent yields and facile separation of the catalyst from the reaction mixture are two of the most appealing features of this approach. Thus, bioactive molecules with pyran units may have fascinating biological properties. An efficient and green strategy for the one-pot synthesis of bioactive 4H-pyran compounds has been described. The pyrans heterocycles were produced by multicomponent reaction of ethyl acetoacetate, malononirile and substituted aromatic aldehydes in the presence of MgAl2O4 spinel nanocatalyst under mild conditions (room temperature and green solvents). MgAl2O4 nanocatalytst was prepared from Mg/Al-LDH with a molar ratio 3 of Mg2+/Al3+ by thermal treatment at 800°C. The samples were investigated by various characterization techniques such as XRD, TG-dTG, FT-IR and N2 adsorption-desorption. The following are the appealing qualities of this unique strategy including good to exceptional yields, and ease of separation of catalyst from the reaction mixture. Thus, the obtained bioactive compounds containing pyrans motif can be exhibiting interested biological activities. Methods: The substituted 4H-pyran compounds were carried out by condensation reaction of substituted aromatic aldehydes, ethyl ethyl acetoacetate and malononirile by using MgAl2O4 nanocatalyst under sustainable conditions. Objective: To develop an efficient methodology for synthesis of 4H-pyran heterocyclic molecules may have interesting applications in biology using a heterogeneous and easily synthesized catalyst. Results: This procedure outlines the synthesis of bioactive compounds in good yields and with ease of catalyst extraction from the reaction mixture under sustainable reaction conditions. Conclusion: In conclusion, it is important to reiterate that a spinel nanostucture has been successfully prepared and fully characterized using different physicochemical analysis methods. The catalytic activity of this heterogeneous catalyst was examined through the one-pot condensation of aryl benzaldehyde, malononitrile and ethyl acetoacetate. Therefore, we have developed a green method for the preparation of 4H-pyrans derivatives using MgAl2O4 as an efficient heterogeneous catalyst. The reactions were performed under green conditions, which have many benefits such as undergoing a simple procedure, good to excellent yields and easy to separate the catalyst.


2022 ◽  
Vol 32 (1) ◽  
Author(s):  
Hellna Tehubijuluw ◽  
Riki Subagyo ◽  
Yuly Kusumawati ◽  
Didik Prasetyoko

AbstractPhotocatalytic degradation of Methylene Blue (MB) by zinc oxide/zeolite socony mobile-5 (ZnO/ZSM-5) composites was investigated. The ZSM-5 material was synthesized from red mud by a two-step hydrothermal method to which ZnO loadings at different mass ratios were subsequently performed. Characterizations using X-ray diffraction (XRD), Fourier transform infrared spectroscopy, and scanning electron microscopy were carried out to identify the formation of ZSM-5 and ZnO/ZSM-5. ZSM-5 and ZnO/ZSM-5 have cubic microcrystallite morphologies. ZnO loading in the ZnO/ZSM-5 composites was successfully performed and confirmed by the appearance of wurtzite peaks in the XRD spectra that matched the Joint Committee on Powder Diffraction Standards data. The presence of ZnO in ZSM-5 leading resulted in a decrease in the surface area and pore size as confirming by nitrogen adsorption-desorption isotherm experiments. The band gap of the samples was measured using UV-Vis diffuse reflectance spectroscopy. The optimum photocatalytic degradation of MB was observed at a ZnO loading of 34% w/w dubbed 34-ZnO/ZSM-5. The influence of the initial concentration of MB was also investigated at 80, 90, and 100 mg L− 1 using 34-ZnO/ZSM-5 and ZSM-5. Liquid chromatography–mass spectrometry characterization was performed to analyze the degradation products.


Water ◽  
2022 ◽  
Vol 14 (2) ◽  
pp. 171
Author(s):  
Chengtao Li ◽  
Deyi Kong ◽  
Xiaolong Yao ◽  
Xiaotao Ma ◽  
Chunhui Wei ◽  
...  

Adsorbent material was prepared using distillers’ grains (DG), which is a waste product of distilleries. The DG was pre-treated with NaOH and esterification-modified with CS2, which is a commonly used anionic modifier. The structure and morphology of the adsorbent was characterized by FTIR, XRD, EDS, SEM, BET, and zeta potential. The related mechanism of adsorption of malachite green (MG) onto modified distiller’s grains (MDG) was studied by adsorption experiments and molecular simulation techniques. The experimental results showed that CS2 successfully modified the DG fiber, and simultaneously yielded the MDG with a uniform pore distribution. MDG had a considerable adsorption capacity of 367.39 mg/g and a maximum removal rate of 96.51%. After eight adsorption–desorption cycle experiments, the adsorption removal rate of MDG to MG dye remained at 82.6%. The adsorption process could be fitted well by a pseudo-second-order kinetic model (the correlation coefficient R2 > 0.998) and Freundlich isotherm adsorption equation (the correlation coefficient R2 > 0.972). Moreover, the adsorption of MG dye by MDG is a spontaneous, endothermic, and increased entropy process. The results of molecular simulation showed that the mechanism of MG molecules onto MDG was mainly chemical adsorption. The adsorption performance of MG onto MDG was better and more stable than DG. Molecular simulation also provided a theoretical guidance of MDG adsorption–desorption for the research on recycling of DG resources.


Geofluids ◽  
2022 ◽  
Vol 2022 ◽  
pp. 1-15
Author(s):  
Peng Zhang ◽  
Junwei Yang ◽  
Yuqi Huang ◽  
Jinchuan Zhang ◽  
Xuan Tang ◽  
...  

Shale heterogeneity directly determines the alteration ability and gas content of shale reservoirs, and its study is a core research topic in shale gas exploitation and development. In this study, the shale from the Longmaxi Formation from well Ld1 located in western Hunan and Hubei is investigated. The shale’s heterogeneity is analyzed based on shale mineral rocks, microslices, geochemistry, and low-temperature N2 adsorption-desorption. It is found that the shales of the Longmaxi Formation from well Ld1 are mainly composed of siliceous shale, mixed shale, and clayey shale. The three types of shale facies exhibit strong heterogeneity in terms of the occurrence state of organic matter, organic content, mineral composition, microstructure and structure, brittleness, and micropore type. Sedimentation, late diagenesis, and terrigenous input are the main factors influencing the shale’s heterogeneity. With a total organic carbon (TOC) of 0.41%-4.18% and an organic matter maturity ( R o ) of 3.09%-3.42%, the shales of the Longmaxi Formation from well Ld1 are in an overmature stage, and their mineral composition is mainly quartz (5%-66%) and clay minerals (17.8%-73.8%). The main pore types are intergranular pores, intragranular pores, microfractures, and organic pores. The results of the low-temperature N2 adsorption-desorption experiment show that the shale pores are mainly composed of micropores and mesopores with narrow throats and complex structures, and their main morphology is of a thin-necked and wide-body ink-bottle pore. Based on the Frenkel-Halsey-Hill (FHH) model, the pore fractal dimension is studied to obtain the fractal dimension D 1 (2.73-2.76, mean 2.74) under low relative pressure ( P / P 0 ≤ 0.5 ) and D 2 (2.80-2.89, mean 2.85) under high relative pressure ( P / P 0 > 0.5 ). The shales of the Longmaxi Formation in the study area have a strong adsorption and gas storage capacity; however, the pore structure is complex and the connectivity is poor, which, in turn, imposes high requirements on reservoir reformation measures during exploitation. Moreover, the fractal dimension has a positive correlation with organic matter abundance, TOC, clay mineral content, and pyrite content and a negative correlation with quartz content. Since the organic matter contained in the shales of the Longmaxi Formation in the study area is in the overmature stage, the adsorption capacity of the shales is reduced, and the controlling effect of organic matter abundance on the same is not apparent.


2022 ◽  
Vol 9 ◽  
Author(s):  
Yutong Zhu ◽  
Xiaofei Xu ◽  
Jian He ◽  
Jie Guo ◽  
Ke Song

High-effective synthesis of 5-hydroxymethylfurfural (HMF) from carbohydrates is an interesting reaction among biomass valorization. The as-synthesized Ti-SBA-15 catalysts with mesoporous structures showed high catalytic efficiency for the conversion of fructose to HMF. Ti-SBA-15 catalysts with different Si/Ti ratios were characterized by characterization techniques such as elemental analysis, XRD, TEM, N2 adsorption–desorption, NH3-TPD, and pyridine-FTIR. The acidity of Ti-SBA-15 catalysts could be tuned by altering addition amount of titanium. The effects of reaction conditions, including reaction time, temperature, and amount of catalyst, on the conversions of fructose and the yields of HMF were also investigated. It is found that Ti-SBA-15 catalysts whose Si/Ti ratio is 120 gave the best yields of HMF, which demonstrated 100% conversion of fructose with a maximum HMF yield of 82% at 140°C after 1 h. In addition, its catalytic performance was retained after 5 recycles in fructose conversion reaction, proving its good catalytic stability.


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