In this work, spent coffee grounds (SCG) were treated using sulfuric acid hydrolysis in order to isolate the sulfuric acid lignin (SAL). The reactivity of SAL was improved through phenolation and acetylation. Spectroscopic analysis showed that the isolated lignin is composed of GHS type and it was characterized by a high amount of (C–C) and β-O-4 bonds. The thermal analysis showed that the phenolated sulfuric acid lignin (Ph-SAL) present higher thermal stability compared to SAL and acetylated sulfuric acid lignin. In addition, the phenolic hydroxyl group content increases from 2.99 to 9.49 mmol/g after phenolation. Moreover, a methylene blue (MB) adsorption test was established in order to find out the sorption capacity of different samples. The study showed that the adsorbed amount of dye increase after the chemical modification of SAL, especially after phenolation. The removal efficiency was enhanced after modification to reach 99.62% for Ph-SAL. The evaluation of the adsorption experimental data with the theoretical models of Langmuir and Freundlich showed that the best fitting was expressed by the Langmuir model for all samples. Finally, this study showed that lignin isolated from SCG can be simply and easily chemical modified and exhibits excellent adsorption ability towards cationic dyes (MB) in aqueous solutions. As a renewable, low-cost, and natural biomass material, lignin from SCG shows a promising practical and economical application of biomass in the field of wastewater purification.
Porous materials constitute an attractive research field due to their high specific surfaces; high chemical stabilities; abundant pores; special electrical, optical, thermal, and mechanical properties; and their often higher reactivities. These materials are currently generating a great deal of enthusiasm, and they have been used in large and diverse applications, such as those relating to sensors and biosensors, catalysis and biocatalysis, separation and purification techniques, acoustic and electrical insulation, transport gas or charged species, drug delivery, and electrochemistry. Porous carbons are an important class of porous materials that have grown rapidly in recent years. They have the advantages of a tunable pore structure, good physical and chemical stability, a variable specific surface, and the possibility of easy functionalization. This gives them new properties and allows them to improve their performance for a given application. This review paper intends to understand how porous carbons involve the removal of pollutants from water, e.g., heavy metal ions, dyes, and organic or inorganic molecules. First, a general overview description of the different precursors and the manufacturing methods of porous carbons is illustrated. The second part is devoted to reporting some applications such using porous carbon materials as an adsorbent. It appears that the use of porous materials at different scales for these applications is very promising for wastewater treatment industries.
Nanocrystalline powders of TiO 2 xerogel and aerogel were prepared by using acidmodified sol-gel approach. For TiO 2 aerogel material (TA), the solvent was high temperature supercritically extracted at 300°C and 100 bars. However, the TiO 2 xerogel material (TX) was dried at 200°C and ambient pressure. The effects of the drying processes on the crystalline structure, phase transformation and grain growth were determined by Raman spectroscopy, SAED and Xray diffraction (XRD) analyses using Rietveld refinement method. The TiO 2 aerogel was composed of anatase crystalline structure. The TiO 2 xerogel material was composed of anatase, brookite and small amount of amorphous phase with anatase as dominant phase. The TX sample still contains a relatively high concentration of carbon than that of TA, indicating the amorphous character of TiO 2 xerogel. These materials were applied as catalyst for the degradation of indigo carmine in aqueous medium. Photo-degradation ability of TA and TX was compared to the TiO 2 commercial Degussa P25. The photo-catalytic results showed that the degradation efficiency was in the order TA > P25 > TX. The photo-degradation of indigo carmine followed pseudo first order reaction kinetics. Ó 2017 King Saud University. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
The selective one-step access to fluoroalkylated hexestrol derivatives, nonsteroidal estrogens, is achieved in good to excellent isolated yields under organophotoredox conditions by using the stable and easy to handle Langlois reagent.Furthermore, the challenging selective hydrotrifluoromethylation of styrenes proceeds under mild reaction conditions without the requirement for any additive. We assume that the solvent drives the reaction pathway towards either the reduction or the dimerization of the radical intermediate generated after initial addition of the fluoroalkyl radical to the styrene. The versatility of the developed system is also extended to encompass radical-radical cross-coupling as exemplified here using cyanopyridine. Mechanistic investigations including luminescence and EPR spectroscopy allow to shed the light on the different mechanisms.
Activated carbon obtained from Opuntia ficus indica by sodium hydroxide activation was employed for the adsorption of p-nitrophenol from water. The activated carbons obtained were characterized by Fourier transforms infrared spectroscopy, sorption of nitrogen, scanning electron microscopy, and Boehm titration. Effects of pH, contact time, amount of adsorbent, and temperature on the adsorption of p-nitrophenol were studied. Adsorption isotherms were analyzed using Freundlich, Langmuir, Temkin, and Dubinin-Radushkevich models, and the thermodynamic parameters have been determined. The adsorption of p-nitrophenol was spontaneous, exothermic, and propitious at 15 °C and adopted the pseudo-second order model, and the most credible isotherm was Langmuir’s one. The activated carbon used in this work has good p-nitrophenol adsorption characteristics, and the study of the desorption and reuse of this carbon shows that it retains a removal rate greater than 94% after five cycles of adsorption-desorption.
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