High Selectivity Fuel from Efficient CO2 Conversion by Zn-Modified rGO and Amine-Functionalized CuO as a Photocatalyst.

Reduced graphene oxide (rGO) has been used in copper (II) oxide (CuO)-based photocatalysts as an additive material. An application of this CuO-based photocatalyst is in the CO2 reduction process. The preparation of rGO by a Zn-modified Hummers' method has resulted in a high quality of rGO in terms of excellent crystallinity and morphology. However, implementing Zn-modified rGO in CuO-based photocatalysts for the CO2 reduction process has yet to be studied. Therefore, this study explores the potential of combining Zn-modified rGO with CuO photocatalysts and performing these rGO/CuO composite photocatalysts to convert CO2 into valuable chemical products. The rGO was synthesized by using a Zn-modified Hummers' method and covalently grafted with CuO by amine functionalization with three different compositions (1:10, 1:20, and 1:30) of rGO/CuO photocatalyst. XRD, FTIR, and SEM were used to investigate the crystallinity, chemical bonds, and morphology of the prepared rGO and rGO/CuO composites. The performance of rGO/CuO photocatalysts for the CO2 reduction process was quantitively measured by GC-MS. We found that the rGO showed successful reduction using a Zn reducing agent. The rGO sheet could be grafted with CuO particles and resulted in a good morphology of rGO/CuO, as shown from the XRD, FTIR, and SEM results. The rGO/CuO material showed photocatalytic performance due to the advantages of synergistic components and resulted in methanol, ethanolamine, and aldehyde as fuel with amounts of 37.12, 8730, and 17.1 mmol/g catalyst, respectively. Meanwhile, adding CO2 flow time increases the resulting quantity of the product. In conclusion, the rGO/CuO composite could have potential for large-scale CO2 conversion and storage applications.

Study on optimization of coagulation-flocculation of fish market wastewater using bittern coagulant - response surface methodological approach.

Bittern contains a high ionic strength that can be used as an alternative coagulant in wastewater treatment. The magnesium content in the bittern could promote the removal of suspended particles and nutrients as settleable precipitates. This would create a more compact and manageable sludge. This study investigates the performance of bittern as a coagulant for fish market wastewater treatment. The effectiveness of bittern was evaluated based on the efficiency of pollutants removal and the amount of residual magnesium. The experiments were performed using a standard jar test. Response surface methodology (RSM) based on a two-factor central composite design (CCD) was used to design the experiment. The parameters involved were pH (7.5, 9, and 10.5) and coagulant dose (0.5, 1.5, 2.5 mL L-1). The maximum removal efficiencies (i.e., 93.3% TSS, 87.5% COD, 37.6% ammonium, and 91.3% phosphate) were recorded at pH 10.5 and 1.5 mL L-1 dose of bittern, while the optimum results (desirability value of 0.929) may occur at pH 10.5 and a dose of 1.284 mL L-1. Approximately 51% of struvite and 48% of calcite precipitates were identified in the generated sludge, which can possibly be used as supplementary material in agrochemical industry with further treatment.

Structures and catalytic properties of PtRu electrocatalysts prepared via the reduced RuO2 nanorods array.

Structures and properties of PtRu electrocatalyts, derived from the aligned RuO2 nanorods (RuO2NR), are investigated using scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and cyclic voltammetry toward COads and methanol oxidation. The catalytic activity of methanol oxidation and the CO tolerance are promoted significantly by reducing RuO2 into Ru metal before decorating with Pt. Reduction of RuO2NR was carried out by either thermal decomposition at 650 degrees C in vacuum or H2-reduction at 130 degrees C in low-pressure hydrogen. Reduction assisted by hydrogen allows infiltrating decomposition at low temperature and produces an array of nanorods with rugged walls featuring small Ru nuclei and larger surface area. Pt-RuNR, whose surface Pt:Ru ratio=0.58:0.42 was prepared by decorating with 0.1 mg cm(-2) Pt on the H2-reduced array containing 0.39 mg cm(-2) Ru, demonstrates a favorable combination of CO tolerance and high methanol oxidation activity superior to other RuO2NR-derived catalysts. When compared with a commercial electrocatalyst of PtRu (1:1) alloy (<4 nm), the activity of Pt-RuNR in methanol oxidation is shown to be somewhat lower at potential<0.48 V and higher at potential>or=0.48 V.