Amination of biochar surface from watermelon peel for toxic chromium removal enhancement

Watermelon peel residues were used to produce a new biochar by dehydration method. The new biochar has undergone two methods of chemical modification and the effect of this chemical modification on its ability to adsorb Cr(VI) ions from aqueous solution has been investigated. Three biochars, Melon-B, Melon-BO-NH_2 and Melon-BO-TETA, were made from watermelon peel via dehydration with 50% sulfuric acid to give Melon-B followed by oxidation with ozone and amination using ammonium hydroxide to give Melon-BO-NH_2 or Triethylenetetramine(TETA) to give Melon-BO-TETA. The prepared biochars were characterized by BET, BJH,SEM, FT-IR, TGA, DSC and EDAX analyses. The highest removal percentage of Cr(VI) ions was 69% for Melon-B,98% for Melon-BO-NH_2 and 99% for Melon-BO-TETA biochars of 100 mg·L~(-1) Cr(VI) ions initial concentration and 1.0 g·L~(-1) adsorbents dose. The unmodified biochar(Melon-B) and modified biochars(Melon-BO-NH_2 and Melon-BO-TETA) had maximum adsorption capacities(Qm) of 72.46, 123.46, and 333.33 mg·g~(-1), respectively.The amination of biochar reduced the pore size of modified biochar, whereas the surface area was enhanced.The obtained data of isotherm models were tested using different error function equations. The Freundlich,Tempkin and Langmuir isotherm models were best fitted to the experimental data of Melon-B, Melon-BO-NH_2 and Melon-BO-TETA, respectively. The adsorption rate was primarily controlled by pseudo-second–order rate model. Conclusively, the functional groups interactions are important for adsorption mechanisms and expected to control the adsorption process. The adsorption for the Melon-B, Melon-BO-NH_2 and Melon-BO-TETA could be explained for acid–base interaction and hydrogen bonding interaction.     

Open Sesame? Open access priorities,incentives, and policies among higher education institutions in the United Arab Emirates

Scientometrics - Higher education institutions (HEIs) have an instrumental role in the move towards Open Access (OA) by shaping the national strategies, policies, and agendas. This study sets out...     

Synthesis of cadmium sulfide‐reduced graphene oxide nanocomposites by pulsed laser ablation in liquid for the enhanced photocatalytic reactions in the visible light

The large‐scale applications of cadmium sulfide (CdS) nanoparticles (NPs) as a photo‐catalyst are limited by their poor stability (high aggregation tendency) and consequent reduction in the surface area and increased rate of recombination of photoinduced electron‐hole pairs, despite its inherent positive feature of being visible light active. It has been reported that the photocatalytic performance of CdS can be considerably improved if CdS is made as a composite material with reduced graphene oxide (rGO) in an optimum ratio. In this work, for the first time, we adopted the technique of pulsed laser ablation in liquids (PLAL) to synthesize highly pure CdS NPs and the required CdS/rGO nanocomposites using high purity (99.9%) microstructured CdS and graphene oxide as chemical precursors. PLAL is a simple and rapid 1‐step synthesis process (where the reaction time is reduced from several hours to a few minutes), which does not require high temperature, toxic chemicals, and the final treatment to remove the unwanted by‐products. The optical and morphological characterizations revealed that the anchoring of CdS on rGO transformed the CdS/rGO composite into an efficient photo‐catalyst by enhancing the following positive attributes required for a good photo‐catalyst: (1) The inherent tendency of aggregation of CdS is considerably reduced; CdS NPs with an average grain size of 20 nm are well placed on the rGO sheets; and hence, the surface area of the catalyst was significantly increased to provide more active sites. (2) The reduced rate of photoinduced electron‐hole recombination manifested in the photoluminescence spectrum indicated the effective charge separation. (3) The enhanced light absorption in the visible/infrared region ensured the effectiveness of this material in naturally abundant solar radiation. In the CdS/rGO composite, the rGO sheets play the role of a supporting matrix, cocatalyst, and electron acceptor for CdS. To evaluate the photo‐catalytic performance of CdS/rGO, we applied it as a visible light‐driven photo‐catalyst for degrading methylene blue dye and found that CdS/rGO nanocomposite was more efficient than pure CdS in the visible spectral region. Therefore, PLAL provides a simple and 1‐step route to synthesize high‐purity visible light–driven photo‐catalysts and solar cell material.     

Photocatalytic degradation of methyl orange dye by NiFe<Subscript>2</Subscript>O<Subscript>4</Subscript> nanoparticles under visible irradiation: effect of varying the synthesis temperature

Nanoparticles of nickel ferrites (NiFe₂O₄) were synthesized at different temperature of synthesis (25, 50 and 80 °C) through the chemical co-precipitation method. The synthesized powders were characterized using X-ray diffraction for crystallite size and lattice parameter calculation. It reveals the presence of cubic spinel structure of ferrites with crystallite size between 29 and 41 nm. Transmission electron microscopy and scanning electron microscopy showed uniform distribution of ferrite particles with some agglomeration. The Fourier-transform infrared spectroscopy showed absorption bonds, which were assigned to the vibration of tetrahedral and octahedral complexes. Raman spectroscopy is used to verify that we have synthesized ferrite spinels and determines their phonon modes. The thermal decomposition of the NiFe₂O₄ was investigated by TGA/DTA. The optical study UV–visible is used to calculate the band gap energy. Magnetic measurements of the samples were carried out by means of vibrating sample magnetometer and these studies reveal that the formed nickel ferrite exhibits ferromagnetic behavior. Photoluminescence showed three bands of luminescence located at 420, 440 and 535 nm. The photocatalytic properties of nickel ferrite (NiFe₂O₄) nanoparticles were evaluated by studying the photodecomposition of methyl orange as organic pollutant models and showed a good photocatalytic activity.     

Antifungal activity of edible coating made from chitosan and lactoperoxidase system against Phomopsis sp. RP257 and Pestalotiopsis sp. isolated from mango

Lactoperoxidase system (LPOS) was incorporated into chitosan solutions (0.5, 1, and 1.5%) to protect mangoes against two strains of fungi. Coating solutions effectiveness in vitro (in Petri dish) and in vivo (on mango) were studied on fungal (Phomopsis sp. RP257 and Pestalotiopsis sp.) growth isolated from mango cv Amelie. In vitro, chitosan concentration at least 1% containing or not LPOS effectively inhibited Pestalotiopsis sp. growth at 100%. Presence of LPOS or Lactoperoxydase system with iodine (LPOSI) in chitosan at 0.5% increased the percentage of inhibition from 26 to 93%. Edible films with LPOS inhibited Phomopsis sp. RP257 particularly when LPOS was incorporated in chitosan concentrations of 1 and 1.5%. Iodine did not influenced antifungal activity of LPOS against Pestalotiopsis sp. but decreased activity antifungal toward Phomopsis sp. RP257. The properties (water vapor permeability and mechanical properties) of chitosan films were not significantly changed by the incorporation of the enzyme system. in vivo condition, chitosan coating at 1 and 1.5% with or without enzyme system was sufficient to inhibit totally (100%) Pestalotiopsis sp. and was 60% efficient against Phomopsis sp. with chitosan only at 1 and 1.5%. However, when coating solution mainly at 1 and 1.5% was enhanced by LPOS with or without iodine, it inhibited totally (100%) Phomopsis sp. RP257. The presence of iodine slightly reduced antifungal activity against Phomopsis sp. RP257.     

Inorganic thermoelectric materials: A review

Thermoelectric generator, which converts heat into electrical energy, has great potential to power portable devices. Nevertheless, the efficiency of a thermoelectric generator suffers due to inefficient thermoelectric material performance. In the last two decades, the performance of inorganic thermoelectric materials has been significantly advanced through rigorous efforts and novel techniques. In this review, major issues and recent advancements that are associated with the efficiency of inorganic thermoelectric materials are encapsulated. In addition, miscellaneous optimization strategies, such as band engineering, energy filtering, modulation doping, and low dimensional materials to improve the performance of inorganic thermoelectric materials are reported. The methodological reviews and analyses showed that all these techniques have significantly enhanced the Seebeck coefficient, electrical conductivity, and reduced the thermal conductivity, consequently, improved ZT value to 2.42, 2.6, and 1.85 for near-room, medium, and high temperature inorganic thermoelectric material, respectively. Moreover, this review also focuses on the performance of silicon nanowires and their common fabrication techniques, which have the potential for thermoelectric power generation. Finally, the key outcomes along with future directions from this review are discussed at the end of this article.