Long-term performance of surface impregnation of reinforced concrete structures with silane

The South Asia Research and Information Institute (SARII) in Dallas, Texas, USA, organizes a one-day conference on ”Cities, Courts, and Saints: Muslim Cultures of South Asia” on Saturday 22 September 2012, 09.00–17.00. The conference is co-organised by the The Asian Studies Program at Southern Methodist University, also in Dallas. Venue for the  conference: McCord Auditorium, Dallas Hall, Southern Methodist University. his conference brings together the leading historians of South Asia and sp..

Long-term performance of surface impregnation of reinforced concrete structures with silane

This is the author’s version of a work that was accepted for publication in the journal, Construction and Building Materials. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published at: http://dx.doi.org/10.1016/j.conbuildmat.2013.07.038Silanes can act as hydrophobic pore liners for reinforced concrete (RC) structures. They can significantly reduce the depth of chloride penetration, a major cause of steel reinforcement corrosion. However, there is little published information on their long-term performance. Thirty-two concrete cores were extracted from eight full-scale RC bridge supporting cross-beams that were treated with silane 20 years ago. Their water absorption by capillarity was measured and compared with sixteen control cores extracted from four non-silane treated RC cross-beams constructed at the same time. Results show that silanes may provide a residual protective effect against water even after 20 years of service

SARS-CoV-2 Receptor ACE2 Is an Interferon-Stimulated Gene in Human Airway Epithelial Cells and Is Detected in Specific Cell Subsets across Tissues.

There is pressing urgency to understand the pathogenesis of the severe acute respiratory syndrome coronavirus clade 2 (SARS-CoV-2), which causes the disease COVID-19. SARS-CoV-2 spike (S) protein binds angiotensin-converting enzyme 2 (ACE2), and in concert with host proteases, principally transmembrane serine protease 2 (TMPRSS2), promotes cellular entry. The cell subsets targeted by SARS-CoV-2 in host tissues and the factors that regulate ACE2 expression remain unknown. Here, we leverage human, non-human primate, and mouse single-cell RNA-sequencing (scRNA-seq) datasets across health and disease to uncover putative targets of SARS-CoV-2 among tissue-resident cell subsets. We identify ACE2 and TMPRSS2 co-expressing cells within lung type II pneumocytes, ileal absorptive enterocytes, and nasal goblet secretory cells. Strikingly, we discovered that ACE2 is a human interferon-stimulated gene (ISG) in vitro using airway epithelial cells and extend our findings to in vivo viral infections. Our data suggest that SARS-CoV-2 could exploit species-specific interferon-driven upregulation of ACE2, a tissue-protective mediator during lung injury, to enhance infection

An investigation of polarity reversal in the zinc-iron galvanic cell

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