Efeitos do tipo, tamanho e teor de agregado graúdo no módulo de deformação do concreto de alta resistência

O concreto, material de composição heterogênea e complexa, é o principal insumo em construções. Do ponto de vista estrutural, ele tem como propriedade principal sua resistência. O estudo do comportamento do concreto, baseado em estudos conceituais da resistência granular, pode conduzir a um projeto estrutural mais seguro e de melhor utilização do material. Este trabalho expõe os resultados de um estudo conduzido para avaliar os efeitos do tipo, tamanho e teor de agregado graúdo no módulo de deformação do concreto de alta resistência. A mistura de concreto estudada contém agregados de basalto e de granito com dimensões máximas características de 9,5 mm e 19 mm e relação água/cimento de 0,35. O módulo de elasticidade do material foi determinado usando o trecho inicial linear da curva Carga-CMOD (deslocamento de abertura da boca da fissura) no ensaio de flexão com três pontos em viga entalhada no meio do vão, seguindo a proposta do comitê técnico 89-FMT da RILEM (Internacional Union of Testing and Research Laboratories for Materials and Structures).

Human aging and somatic point mutations in mtDNA: a comparative study of generational differences (grandparents and grandchildren)

The accumulation of somatic mutations in mtDNA is correlated with aging. In this work, we sought to identify somatic mutations in the HVS-1 region (D-loop) of mtDNA that might be associated with aging. For this, we compared 31 grandmothers (mean age: 63 ± 2.3 years) and their 62 grandchildren (mean age: 15 ± 4.1 years), the offspring of their daughters. Direct DNA sequencing showed that mutations absent in the grandchildren were detected in a presumably homoplasmic state in three grandmothers and in a heteroplasmic state in an additional 13 grandmothers; no mutations were detected in the remaining 15 grandmothers. However, cloning followed by DNA sequencing in 12 grandmothers confirmed homoplasia in only one of the three mutations previously considered to be homoplasmic and did not confirm heteroplasmy in three out of nine grandmothers found to be heteroplasmic by direct sequencing. Thus, of 12 grandmothers in whom mtDNA was analyzed by cloning, eight were heteroplasmic for mutations not detected in their grandchildren. In this study, the use of genetically related subjects allowed us to demonstrate the occurrence of age-related (> 60 years old) mutations (homoplasia and heteroplasmy). It is possible that both of these situations (homoplasia and heteroplasmy) were a long-term consequence of mitochondrial oxidative phosphorylation that can lead to the accumulation of mtDNA mutations throughout life.