Enhanced ductility of Mg–3Al–1Zn alloy reinforced with short length multiwalled carbon nanotubes using a powder metallurgy method

Mg–3Al–1Zn–CNTs composites, with different weight fractions(0.25–1.0 wt%) of carbon nanotubes(CNTs) were successfully fabricated via a powder metallurgy method. The processing parameters were adopted in such a way to have uniform dispersion of short length CNTs without any damage, as well as re fi ned and dissolved β phases structures throughout the composite matrix. The composite exhibited impressive increase in microhardness(about+23%) and tensile failure strain value(about+98%) without signi fi cant compromise in tensile strength, compared to the un-reinforced Mg–3Al–1Zn alloy. The synthesized composites can be used in automotive and aerospace industries due to their low density and high speci fic strength.     

新型多孔聚苯胺在超级电容器电极材料中的应用

通过一个简便的方法,将苯胺单体在含氯化钾(KCl)的盐酸溶液中聚合制备出多孔聚苯胺(polyaniline,PANI).以KC1作为形成多孔聚苯胺的赝模板,既有效地避免了有机溶剂和硬/软模板的使用,又减轻了对环境的污染.由于具有独特的多孔结构和相互交错的纳米棒结构,多孔聚苯胺的比表面积较大,显示出良好的电化学性能.电化...     

Strength of Concrete Filled Steel Tubular Columns

Introduction The steel tube in a concrete filled tubular column (CFT) acts as both longitudinal and lateral reinforcement, and is thus subjected to biaxial stresses of longitudinal compression and hoop tension. At the same time, con- crete is stressed tri…     

De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes

Megalencephaly-capillary malformation (MCAP) and megalencephaly-polymicrogyria-polydactyly-hydrocephalus (MPPH) syndromes are sporadic overgrowth disorders associated with markedly enlarged brain size and other recognizable features. We performed exome sequencing in 3 families with MCAP or MPPH, and our initial observations were confirmed in exomes from 7 individuals with MCAP and 174 control individuals, as well as in 40 additional subjects with megalencephaly, using a combination of Sanger sequencing, restriction enzyme assays and targeted deep sequencing. We identified de novo germline or postzygotic mutations in three core components of the phosphatidylinositol 3-kinase (PI3K)-AKT pathway. These include 2 mutations in AKT3, 1 recurrent mutation in PIK3R2 in 11 unrelated families with MPPH and 15 mostly postzygotic mutations in PIK3CA in 23 individuals with MCAP and 1 with MPPH. Our data highlight the central role of PI3K-AKT signaling in vascular, limb and brain development and emphasize the power of massively parallel sequencing in a challenging context of phenotypic and genetic heterogeneity combined with postzygotic mosaicism.     

Electrical conductivity retention and electrochemical activity of CSA doped graphene/gold nanoparticle@ polyaniline composites

This paper reports the synthesis of CTAB mediated CSA doped PANI and GN/GNP@ PANI composite nanofibers. The as synthesized composite nanofibers were examined by TEM, SEM, XRD, Raman spectroscopy; UV–visible diffused reflectance spectroscopy and TGA. The CTAB mediated CSA doped composite nanofibers showed 59% higher DC electrical conductivity at ambient temperature than that of PANI,which might be due to the enhancement in the mobility of the charge carriers and reduction in hopping distance in the composite system. The CTAB mediated CSA doped composite nanofibers compared to PANI was observed to be showing enhanced DC electrical conductivity retention after various cycles of heating, suggesting an enhancement in thermal stability of the composite structure, which could be attributed to the synergistic effect of GN,GNP and PANI. Additionally, the composite nanofibers showed greater electrochemical activity and better capacitive performance and reduced optical bandgap than that of PANI.     

Genome assembly comparison identifies structural variants in the human genome

Numerous types of DNA variation exist, ranging from SNPs to larger structural alterations such as copy number variants (CNVs) and inversions. Alignment of DNA sequence from different sources has been used to identify SNPs and intermediate-sized variants (ISVs). However, only a small proportion of total heterogeneity is characterized, and little is known of the characteristics of most smaller-sized (<50 kb) variants. Here we show that genome assembly comparison is a robust approach for identification of all classes of genetic variation. Through comparison of two human assemblies (Celera's R27c compilation and the Build 35 reference sequence), we identified megabases of sequence (in the form of 13,534 putative non-SNP events) that were absent, inverted or polymorphic in one assembly. Database comparison and laboratory experimentation further demonstrated overlap or validation for 240 variable regions and confirmed >1.5 million SNPs. Some differences were simple insertions and deletions, but in regions containing CNVs, segmental duplication and repetitive DNA, they were more complex. Our results uncover substantial undescribed variation in humans, highlighting the need for comprehensive annotation strategies to fully interpret genome scanning and personalized sequencing projects.     

The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia

Anonychia and hyponychia congenita (OMIM 206800) are rare autosomal recessive conditions in which the only presenting phenotype is the absence or severe hypoplasia of all fingernails and toenails. After determining linkage to chromosome 20p13, we identified homozygous or compound heterozygous mutations in the gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, in eight affected families. Rspo4 expression was specifically localized to developing mouse nail mesenchyme at embryonic day 15.5, suggesting a crucial role in nail morphogenesis.     

Advancements of Nano-Hydroxyapatite in Sports Medicine from Bone Injury Perspectives

Nanotechnology has revolutionized the field of biology and medicine in the 21st century.Bone injury incidences during sports activities are common,and they are ...     

Multi-seed key distribution scheme test

The key problem of securing multieast is to generate, distribute and update Session Encryption Key（SEK）. Polynomial expansion with multi-seed （MPE） scheme is an approach which is based on Polynomial expansion （PE） scheme and overcomes PE＇s shortage. Its operation is demonstrated by using multi-seed, the group member is partitioned to many subgroups. While updating the SEK, computation is needed only in one of subgroups, the other of them will use the computation history to update their SEK. The key problems to design a MPE scheme application includes to find a feasible one way function as well as to generate a Strict Prime Number （SPN）. Those technologies with multi-seed and computation history concepts make MPE as a good choice in practical applications. A prototype test system is designed and solutions of all above mentioned problems are included in this proposed paper.