Synthesis of gamma irradiated acrylic acid-grafted-sawdust (SD-g-AAc) for trivalent chromium adsorption from aqueous solution.

Water pollution caused by chromium released from tannery is a serious concern to the environment and public health. Chromium removal from tannery effluent is a crying need before discharging to the surface water. In this study, acrylic acid-grafted sawdust was prepared by Tectona grandis sawdust grafting with acrylic acid employing gamma irradiation in the presence of air and Mohr's salt. It was treated with NaOH and the characterization of surface morphology and functional groups of modified sawdust was studied by SEM and FTIR.. The effects of solution pH, adsorbent dosage, adsorption time, and initial Cr(III) ion concentration were investigated by batch sorption studies. The process was found to be pH, temperature and concentration dependent. Langmuir and Freundlich isotherms were applied to realize the adsorption process in depth, and it was found that the Langmuir isotherm model fitted well with experimental data (R2 value of 0.983). The maximum monolayer adsorption capacity of acrylic acid-grafted sawdust for Cr(III) from aquous solution was found to be 21.55 mg g-1 at 25 °C. Pseudo-first-order and pseudo-second-order kinetic models were employed to analyze the kinetics of the process, and it was found that the experimental process followed the pseudo-second-order kinetic model, i.e. chemisorption. This study revealed that acrylic acid-grafted sawdust has a decent potential for the removal of Cr(III) from tannery effluents.

Characterization and application of synthesized calcium alginate-graphene oxide for the removal of Cr3+, Cu2+ and Cd2+ ions from tannery effluents.

Environmental sustainability has gained acceptance to achieving the goal of a secure ecosystem with a reliable management system. Heavy metal remediation of aqueous streams is of special concern due to the intractability and persistence in the environment. Adsorption is a potential alternative to the existing inefficient conventional technologies for the removal and recovery of metal ions from aqueous solutions and becomes vital to align with the Sustainable Development Goals (SDGs) and mitigate the adverse environmental and social impacts. Calcium Alginate-Graphene oxide (CA-GO) composite has been synthesized for the adsorption of heavy metals including Cr3+, Cu2+, and Cd2+ ions from tannery effluents. Graphene oxide is prepared from commercial graphite powder and reacted with sodium alginate and calcium chloride to form the beads of CA-GO composite. The developed composite was characterized by FTIR, elemental analysis, SEM, XRD analysis, and Raman spectroscopy. Moreover, the effect of pH, adsorbent dosage, contact time, and initial concentration of metal ions on the adsorption capacity were investigated through batch experiments. At a pH>3.0 (pHzpc), the carboxyl group of CA-GO was deprotonated to make the surface negatively charged and facilitate metal adsorption. The optimum pH and maximum adsorption capacity of CA-GO for removal of Cr(III), Cu(II), and Cd(II) were 4.5, 6.0, and 7.0, and 90.58, 108.57, and 134.77 mg g-1, respectively. The kinetics, adsorption isotherms, and thermodynamics were studied to determine the adsorption mechanism. The kinetic of adsorption adopted the second-order model. Thermodynamic parameter were calculated and the adsorption process was determined to be exothermic and spontaneous at room temperature. The developed composite has been efficaciously applied for the removal of metal ions and pollution from real tannery effluents.

Effect of successive recycling and reuse of acid liquor for the synthesis of graphene oxides with higher oxygen-to-carbon ratios.

Graphene has recently drawn exponential attention due to its surprising physicochemical properties and diversified field of applications. Although graphene oxides (GOs), itself is an exclusive material, it is also an intermediate product for the production of reduced graphene oxides (rGOs), graphene and their derivatives, which are other more superficial materials. In this study, GOs with higher oxygen to carbon ratios were synthesized following the Tour method, where the excess feed acid liquor (FAL) of mixed concentrated sulfuric and orthophosphoric acids at a ratio of 90:10 was recovered from the reaction slurries by applying the centrifugation technique. About 80-90 % of the FAL was recycled and reused as feed for the subsequent batches. The changes in the properties of FAL for the five consecutive recycling and reuse were studied. The properties of recycled FALs were investigated by measuring density, moisture content, pH, and ion concentration. The consecutive recycling of FALs tends to increase the moisture content about 0.5% in each recycles. Ion-chromatography (IC) was used to measure the variation in SO42- and PO43- ions in the FALs. The H2SO4 reacts with KMnO4 and crystalized out from the recovered FAL faster than the phosphoric acid. So, sulfuric acid content in the makeover FALs must be greater than primary FAL. The product GOs were characterized using FT-IR, FT-Raman, UVVis, STA, SEM, XPS, Zeta-potential, and particle size analyzers. The variation of the properties of GOs with the changes in the reaction parameters such as temperature and time were investigated and correlated with the product yield. It was observed that the effect of temperature on the reaction rate was found to be negatively and positive with the reaction time. The oxygen-to-carbon atomic ratio from XPS analysis was found 66.7%, which supported the increase in product yields 66.9% in the experimental results. The effect of acid concentration, reaction temperature, and time on the GOs properties were satisfactory, correlated, and easily controllable with the reaction conditions. A higher extent of oxidation and enhanced product yields 65-70% were observed at 60-70 °C and 14-18 h. A mixture of nano- and macro-molecular GOs was obtained, and their compositions were easily controllable and separable by controlling the reaction conditions. A correlation was made among the properties of synthesized GOs, FAL, and recycled FAL and reaction conditions.

Aggregation-induced emission enhancement (AIEE) of tetrarhenium(I) metallacycles and their application as luminescent sensors for nitroaromatics and antibiotics.

The self-assembly of tetrarhenium metallacycles [{Re(CO)3}2(µ-dhaq)(µ-N-N)]2 (3a, N-N = 1,3-bis(1-butylbenzimidazol-2-yl)benzene; 3b, N-N = 1,3-bis(1-octylbenzimidazol-2-yl)benzene), (H2-dhaq = 1,4-dihydroxy-9,10-anthraquinone) and [{Re(CO)3}2(µ-thaq)(µ-N-N)]2 (4, N-N = 1,3-bis(1-butylbenzimidazol-2-yl)benzene), (H2-thaq = 1,2,4-trihydroxy-9,10-anthraquinone) under solvothermal conditions is described. The metallacycles 3a,b and 4 underwent aggregation-induced emission enhancement (AIEE) in THF upon the incremental addition of water. TEM images revealed that metallacycle 3a in a 60% aqueous THF solution formed rectangular aggregates with a wide size distribution, while a 90% aqueous THF solution resulted in the formation of a mixture of nanorods and amorphous aggregates due to rapid and abrupt aggregation. UV-vis and emission spectral profiles supported the formation of nanoaggregates of metallacycles 3a,b and 4 upon the gradual addition of water to a THF solution containing metallacycles. Further studies indicated that these nanoaggregates were excellent probes for the sensitive and selective detection of nitro group containing picric acid (PA) derivatives as well as antibiotics.

Electrically insulating pore-suspending membranes on highly ordered porous obtained from vesicle spreading.

Pore-suspending membranes on porous alumina substrates with pore diameters of 60 nm were prepared by fusion of vesicles on a (cholesterylpolyethylenoxy)thiol-functionalized surface, and their functionality demonstrated by the activity of the proton pump bacteriorhodopsin.