Characterization of ZrC reinforced AA6061 alloy composites produced using stir casting process

In the present study, effect of ZrC vol.% on mechanical properties of AA6061 metal matrix composites (MMCs) produced via stir casting technique was investigated. The vol.% of ZrC particles was varied as 5,10 and 15. The composites were characterized for its microstructure and mechanical properties and their relationships were obtained. The scanning electron microscope (SEM) images revealed uniform distribution and good bonding between the AA6061 alloy and the ZrC particles. The mechanical properties of the AA6061 alloy was found to significantly improve with the addition of ZrC particles from 5 to 15 vol.%, the hardness increased from 32 to 68 HV, yield strength increased from 50 to 86 MPa and the ultimate tensile strength increased from 118 to 165 MPa. However, the % of elongation of the composite samples decreased with 15 vol.% addition of ZrC particles. Sliding wear behaviour of the composites was investigated using a pin-on-disc wear tester at a load of 9.8 N and addition of ZrC particles was significantly found to reduce the wear rate of AA6061 alloy.

     

Dark fermentative biohydrogen production by Acinetobacter junii-AH4 utilizing various industry wastewaters

Hydrogen (H₂) is one of the most promising renewable energy sources, anaerobic bacterial H₂ fermentation is considered as one of the most environmentally sustainable alternatives to meet the potential fossil fuel demand. Bio-H₂ is the cleanest and most effective source of energy provided by the dark fermentation utilizing organic substrates and different wastewaters. In this study, the bio-H₂ production was achieved by using the bacteria Acinetobacter junii-AH4. Further, optimization was carried out at different pH (5.0–8.0) in the presence of wastewaters as substrates (Rice mill wastewater (RMWW), Food wastewater (FWW) and Sugar wastewater (SWW). In this way, the optimized experiments excelled with the maximum cumulative H₂ production of 566.44 ± 3.5 mL/L (100% FWW at pH 7.5) in the presence of Acinetobacter junii-AH4. To achieve this, a bioreactor (3 L) was employed for the effective production of H₂ and Acinetobacter junii-AH4 has shown the highest cumulative H₂ of 613.2 ± 3.0 mL/L, HPR of 8.5 ± 0.4 mL/L/h, HY of 1.8 ± 0.09 mol H₂/mol glucose. Altogether, the present study showed a COD removal efficiency of 79.9 ± 3.5% by utilizing 100% food wastewater at pH 7.5. The modeled data established a batch fermentation system for sustainable H₂ production. This study has aided to achieve an ecofriendly approach using specific wastewaters for the production of bio-H₂.     

MoSe2 nanoflowers as a counter electrode for quantum dots sensitized solar cells

Journal of Materials Science: Materials in Electronics - Layered transition metal dichalcogenides hold tunable and promising photoelectrochemical properties. MoSe2 is a potential candidate of the...     

Pinecone biomass-derived activated carbon: the potential electrode material for the development of symmetric and asymmetric supercapacitors

Activated carbon, from biomass (pinecone), was synthesized by conventional pyrolysis/chemical activation process and utilized for the fabrication of supercapacitor electrodes. The pinecone-activated carbon synthesized with 1:4 ratio of KOH (PAC4) showed an increase in surface area and pore density with a considerable amount of oxygen functionalities on the surface. Moreover, PAC4, as supercapacitor electrode, exhibited excellent electrochemical performances with specific capacitance value ∼185 Fg⁻¹ in 1 M H₂SO₄, which is higher than that of nonactivated pinecone carbon and 1:2 ratio KOH-based activated carbon (PAC2) (∼144 Fg⁻¹). The systematic studies were performed to design various forms of devices (symmetric and asymmetric) to investigate the effect of device architecture and operating voltage on the performance and stability of the supercapacitors. The symmetric supercapacitor, designed utilizing PAC4 in H₂SO₄ electrolyte, exhibited a maximum device-specific capacitance of 43 Fg⁻¹ with comparable specific energy/power and excellent stability (∼96% after 10 000 cycles). Moreover, a symmetric supercapacitor was specially designed using PAC4, as a positive electrode, and PAC2, as a negative electrode, under their electrolytic ion affinity, and which operates in aqueous Na₂SO₄ electrolyte for a wide cell voltage (1.8 V) and showed excellent supercapacitance performances. Also, a device was assembled with poly(3,4-ethylene dioxythiophene) (PEDOT) nanostructure, as positive electrode, and PAC4, as a negative electrode, to evaluate the feasibility of designing a hybrid supercapacitor, using polymeric nanostructure, as an electrode material along with biomass-activated carbon electrode.     

Synthetic Applications of Carbohydrate-derived Donor-Acceptor Cyclopropanes

In this account, we elaborate our group's contribution towards understanding the chemistry of carbohydrate-derived donor-acceptor (DA) cyclopropanes. Our work was mainly focused on the ring opening of these versatile chiral synthons under the influence of Lewis acid promoters like electrophilic halogen species, TMSOTf, BF₃.OEt₂, etc. We studied various modes of ring opening on these DA cyclopropanes, envisaging the access to intriguing molecular architectures. These modes of reaction of the DA cyclopropanes can be controlled by strategically introducing an electron-withdrawing group (EWG) onto the cyclopropane ring, which could direct the ring cleavage by polarizing the cyclopropane C−C bond. Our studies also revealed that the ring opening is sluggish in the absence of an EWG. Using this concept, we demonstrated the synthesis of various biologically interesting molecular skeletons, viz., glycoamino acids (GAA), GAA nucleotides, α-levoglucosan amino acid, and septano-oligosaccharides, with high selectivity. We also applied our understanding to the first stereoselective synthesis of (S)-(−)-longianone and confirmed its absolute configuration. Apart from the inherently activated DA cyclopropanes, we introduced the in situ generation of DA cyclopropanes, starting from vinylcyclopropanes (VCPs). The ring-opening and ring-expansion chemistry of these easily accessible synthons was studied. The chemistry developed for carbohydrate-fused cyclopropanes was also applied for carbohydrate-derived spiro-cyclopropanes. The Lewis-acid-mediated ring opening of spiro-DA-cyclopropanes enabled easy access to fused furopyrans and spirolactones.