Probing the pyrolysis process of rice straw over a “Dual-Catalyst Bed” for the production of fuel gases and value-added chemicals

Rice straw is an agricultural byproduct primarily produced in Asian regions. It is crucial to discover an effective method for converting this waste into chemicals that can be utilized to substitute goods derived from fossil fuels. Pyrolysis serves as an interesting procedure to obtain bio-oil from this rice straw. The composition of the bio-oil obtained after the pyrolysis procedure contains a small quantity of value-added chemicals in addition to various gas components in the gas product. Therefore, the development of catalytic systems that improve this pyrolytic reaction is mandatory. Herein, the design of a dual catalyst bed (CEM/ZSM-5) that catalyzes the volatiles that it releases has been developed. The highest output of 42.1 wt.% of bio-oil, 29.9 wt.% of gases and 28.0 wt.% of bio-char was obtained. Nevertheless, the inclusion of single zeolites to biomass yields biofuel outputs of 42.8 wt.%, gas yields of 27.7 wt.%, and a bio-char yielding of 29.5 wt.%. Additionally, the addition of cement to biomass results in a bio-oil yield of 40.4 wt.% and 30.5 wt.% of gas, along with 29.1 wt.% of char. Regarding pyrolysis gas products, the H2 yield in the produced biogas was increased from 35.9 mL/g to 45.7 mL/g, and the CH4 output was increased from 21.1 mL/g to 27.4 mL/g. The bioenergy output was evaluated employing GC-FID and GC-MS (gas and biofuel). The dual catalytic bed had a significant impact on the contents of the generated biofuel, increasing the quantity of hydrocarbons and other value-added compounds

Jute-derived microporous/mesoporous carbon with ultra-high surface area using a chemical activation process

Here, we report the synthesis of nanoporous carbons (NCs) derived from a low-cost and renewable biomass, jute, by a chemical activation process using KOH. Jute is one of the least expensive and most abundant crops, with a staggering 2.8 million metric tons of jute produced each year. In this study, we synthesize NCs from three different parts of jute fibers through a chemical activation technique using KOH. The NCs prepared from the bottom portion of the fiber show a high surface area (2682 m g) with the presence of both micropores and mesopores. The ultra-high surface area of jute makes it an economically viable, environmentally friendly precursor for NCs, with a wide variety of applications from energy storage to environmental and biomedical applications

Synthesis, Characterization and Enhanced Visible Light Photocatalytic Performance of ZnWO4-NPs@rGO Nanocomposites

ZnWO4 nanoparticles on reduced graphene oxide (ZnWO4-NPs@rGO) nanocomposites were synthesized using the hydrothermal method. Structural, morphological, optical, and photocatalytic studies of the ZnWO4-NPs@rGO nanocomposites were successfully investigated. Photo-catalytic performances of the ZnWO4-NPs@rGO nanocomposites were examined for the degradation of hazardous methylene blue dye (HMBD) in a neutral medium. ZnWO4-NPs@rGO nanocomposites show superior photo-catalytic performances over pure ZnWO4 nanoparticles. ZnWO4-NPs@rGO nanocomposites degrade ~98% dye while pure ZnWO4 nanoparticles degrade ~53% dye in 120 min. The prepared nanocomposites also show excellent recycled photo-catalytic efficiencies over multiple cycles

Reduced Graphene Oxide Supported Zinc Tungstate Nanoparticles as Proficient Electro-Catalysts for Hydrogen Evolution Reactions

The nanocomposites of reduced graphene oxide (rGO) supported zinc tungstate nanoparticles (ZnWO4-NPs) receive considerable attention in electro-catalytic hydrogen evolution reactions (HER) and reveal significantly higher electro-catalytic performances than pure ZnWO4-NPs in alkaline media (i.e., 0.5 M KOH electrolyte). The polarization studies show that the ZnWO4-NPs@rGO nanocomposites exhibit low energy loss and good electrode stability during electrochemical reactions for HER. Furthermore, the Tafel slope of ZnWO4-NPs@rGO nanocomposites is found to be approximately 149 mV/dec, which closely agrees with the reported Tafel values of the noble metal electrocatalyst. In contrast, the performance of the ZnWO4-NPs@rGO nanocomposite is found to be approximately 1.5 times higher than that of ZnWO4-NPs in hydrogen production efficiency. Our results emphasize the significance of the nanocomposites with enhanced electro-catalytic activities by lowering the energy loss during electro-catalysis in an alkaline medium

Reduced Graphene Oxide Supported Zinc Tungstate Nanoparticles as Proficient Electro-Catalysts for Hydrogen Evolution Reactions

The nanocomposites of reduced graphene oxide (rGO) supported zinc tungstate nanoparticles (ZnWO4-NPs) receive considerable attention in electro-catalytic hydrogen evolution reactions (HER) and reveal significantly higher electro-catalytic performances than pure ZnWO4-NPs in alkaline media (i.e., 0.5 M KOH electrolyte). The polarization studies show that the ZnWO4-NPs@rGO nanocomposites exhibit low energy loss and good electrode stability during electrochemical reactions for HER. Furthermore, the Tafel slope of ZnWO4-NPs@rGO nanocomposites is found to be approximately 149 mV/dec, which closely agrees with the reported Tafel values of the noble metal electrocatalyst. In contrast, the performance of the ZnWO4-NPs@rGO nanocomposite is found to be approximately 1.5 times higher than that of ZnWO4-NPs in hydrogen production efficiency. Our results emphasize the significance of the nanocomposites with enhanced electro-catalytic activities by lowering the energy loss during electro-catalysis in an alkaline medium

Development of new copper-64 labeled rhodamine: a potential PET myocardial perfusion imaging agent

Abstract Background Myocardial perfusion imaging (MPI) is one of the most commonly performed investigations in nuclear medicine procedures. Due to the longer half-life of the emerging positron emitter copper-64 and its availability from low energy cyclotron, together with its well-known coordination chemistry, we have synthesized 64Cu-labeled NOTA- and 64Cu-NOTAM-rhodamine conjugates as potential cardiac imaging agents using PET. Results 64Cu-NOTA- and 64Cu-NOTAM-rhodamine conjugates were synthesized using a traightforward and one-step simple reaction. Radiochemical yields were greater than 97% (decay corrected), with a total synthesis time of less than 25 min. Radiochemical purities were always greater than 98% as assessed by TLC and HPLC. These synthetic approaches hold considerable promise as a simple method for 64Cu-rhodamine conjugates synthesis, with high radiochemical yield and purity. Biodistribution studies in normal Fischer rats at 60 min post-injection, demonstrated significant heart uptake and a good biodistribution profile for both the radioconjugates. However, the 64Cu-NOTAM-rhodamine conjugate has shown more heart uptake (~ 10% ID/g) over the 64Cu-NOTA-rhodamine conjugate (5.6% ID/g). Conclusions These results demonstrate that these radioconjugates may be useful probes for the PET evaluation of MPI

Magnetic Nanoparticles—A Multifunctional Potential Agent for Diagnosis and Therapy

Magnetic nanoparticles gained considerable attention in last few years due to their remarkable properties. Superparamaganetism, non-toxicity, biocompatibility, chemical inertness, and environmental friendliness are some of the properties that make iron oxide nanoparticles (IONPs) an ideal choice for biomedical applications. Along with being easily tuneable and a tailored surface for conjugation of IONPs, their physio-chemical and biological properties can also be varied by modifying the basic parameters for synthesis that enhances the additional possibilities for designing novel magnetic nanomaterial for theranostic applications. This review highlights the synthesis, surface modification, and different applications of IONPs for diagnosis, imaging, and therapy. Furthermore, it also represents the recent report on the application of IONPs as enzyme mimetic compounds and a contrasting agent, and its significance in the field as an anticancer and antimicrobial agent