Study comparing the tribological behavior of propylene glycol and water dispersed with graphene nanopowder.

Nanofluids made up of propylene glycol, and water and graphene nanopowder dispersed throughout them are the primary focus of our study. Nanofluids were created by mixing propylene glycol and water in quantities of 100:0, 75:25, and 50:50. The essential fluids used in this experiment were propylene glycol and water. Graphene was dispersed in these three different base fluids at percentages of 0.25 and 0.5, respectively. This body of work's fundamental objective is to explore nanofluids' tribological behavior. This behavior was observed with a pin-on-disc device, and the impact for load on wear, coefficient of friction, and frictional force was investigated. The tests were conducted with weights ranging from 1 to 3 kg. It was revealed that as the load ascended, there was a reduction in the amount of wear, the coefficient of friction, and the frictional force for the most of the samples tested. Still, there was an increase in the amount of wear and friction coefficient, including the frictional force for some of the samples.

Evaluation of protein oxidation and its association with lipid peroxidation and thyrotropin levels in overt and subclinical hypothyroidism.

Both overt (OHT) and subclinical hypothyroid (SHT) disorders have been found to be associated with increased oxidative stress (OXS). Excess thyrotropin [thyroid stimulating hormone (TSH)] is known to directly produce OXS. Increased lipid peroxidation is known to facilitate protein carbonylation. However, the associations between lipid and protein oxidation and elevated TSH levels have not been studied. Thyroid profile, lipid peroxidation as malondialdehyde (MDA) levels and protein carbonylation as protein carbonyls (PCO) were estimated in OHT and SHT groups consisting of 36 patients each, in comparison to 39 euthyroid controls. We also determined the associations between TSH, MDA, and PCO levels in OHT and SHT groups. Increased oxidative damage was evidenced through significant elevations in the concentrations of MDA and PCO in OHT and SHT groups compared to controls (p < 0.01). Both TSH and MDA levels were positively associated with PCO in OHT group. Partial correlation analysis revealed that both excess TSH and increased MDA levels are mutually influencing elevated PCO. The results indicate that there is a simultaneous oxidative damage to lipids and proteins leading to increased MDA and PCO levels in both patient groups. Either of the excess TSH and increased MDA levels are combinably involved in the elevation of PCO in hypothyroidism.