Effects of Mg content on microstructure and mechanical properties of low Zn-containing Al-xMg-3Zn-1Cu cast alloys

Effects of Mg content on the microstructure and mechanical properties of low Zn-containing Al−xMg−3Zn−1Cu cast alloys(x=3−5,wt.%)were investigated.As Mg content increased in the as-cast alloys,the grains were refined due to enhanced growth restriction,and the formation ofη-Mg(AlZnCu)_(2) and S-Al_(2)CuMg phases was inhibited while the formation of T-Mg_(32)(AlZnCu)_(49 )phase was promoted when Mg content exceeded 4 wt.%.The increase of Mg content encumbered the solution kinetics by increasing the size of eutectic phase but accelerated and enhanced the age-hardening through expediting precipitation kinetics and elevating the number density of the precipitates.As Mg content increased,the yield strength and tensile strength of the as-cast,solution-treated and peak-aged alloys were severally improved,while the elongation of the alloys decreased.The tensile strength and elongation of the peak-aged Al−5Mg−3Zn−1Cu alloy exceed 500 MPa and 5%,respectively.Precipitation strengthening implemented by T′precipitates is the predominant strengthening mechanism in the peak-aged alloys and is enhanced by increasing Mg content.

Influence of rare earth on the microstructure and age hardening response of indirect-extruded Mg-5Sn-4Zn alloy

The effects of Ce addition on the microstructure, age hardening response and mechanical properties of an indirect-extruded Mg-5wt.%Sn-4Zn (TZ54) alloy were investigated. Addition of Ce accelerated the aging response with the peak aging time moving from 300 h in TZ54 to 30 h in Mg-5wt.%Sn-4Zn-1Ce (TZE541), while the peak harness was similar to each other. The addition of Ce also caused an increase in the precipitation stability during overageing. Though the tensile strength of extruded TZ54 was improved by t...

DNA Damage Response in Hematopoietic Stem Cell Ageing

Maintenance of tissue-specific stem cells is vital for organ homeostasis and organismal longevity.Hematopoietic stem cells（HSCs） are the most primitive cell type in the hematopoietic system.They divide asymmetrically and give rise to daughter cells with HSC identity（selfrenewal） and progenitor progenies（differentiation）,which further proliferate and differentiate into full hematopoietic lineages.Mammalian ageing process is accompanied with abnormalities in the HSC self-renewal and differentiation.Transcriptional changes and epigenetic modulations have been implicated as the key regulators in HSC ageing process.The DNA damage response（DDR）in the cells involves an orchestrated signaling pathway,consisting of cell cycle regulation,cell death and senescence,transcriptional regulation,as well as chromatin remodeling.Recent studies employing DNA repair-deficient mouse models indicate that DDR could intrinsically and extrinsically regulate HSC maintenance and play important roles in tissue homeostasis of the hematopoietic system.In this review,we summarize the current understanding of how the DDR determines the HSC fates and finally contributes to organismal ageing.