Limiting the consumption of nonrenewable resources and minimizing waste production and associated gas emissions are the main priority of the construction sector to achieve a sustainable future. This study investigates the sustainability performance of newly developed binders known as alkali-activated binders (AABs). These AABs work satisfactorily in creating and enhancing the concept of greenhouse construction in accordance with sustainability standards. These novel binders are founded on the notion of utilizing ashes from mining and quarrying wastes as raw materials for hazardous and radioactive waste treatment. The life cycle assessment, which depicts material life from the extraction of raw materials through the destruction stage of the structure, is one of the most essential sustainability factors. A recent use for AAB has been created, such as the use of hybrid cement, which is made by combining AAB with ordinary Portland cement (OPC). These binders are a successful answer to a green building alternative if the techniques used to make them do not have an unacceptable negative impact on the environment, human health, or resource depletion. The Technique for Order Preference by Similarity to Ideal Solution (TOPSIS) software was employed for choosing the optimal materials' alternative depending on the available criteria. The results revealed that AAB concrete provided a more ecologically friendly alternative than OPC concrete, higher strength for comparable water/binder ratio, and better performance in terms of embodied energy, resistance to freeze-thaw cycles, high temperature resistance, and mass loss due to acid attack and abrasion.
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http://dx.doi.org/10.3390/biomimetics8010058 | DOI Listing |
Cell Rep
January 2025
Molecular Immunology, Justus-Liebig-University Giessen, 35392 Giessen, Germany. Electronic address:
Control of cell proliferation is critical for the lymphocyte life cycle. However, little is known about how stage-specific alterations in cell cycle behavior drive proliferation dynamics during T cell development. Here, we employed in vivo dual-nucleoside pulse labeling combined with the determination of DNA replication over time as well as fluorescent ubiquitination-based cell cycle indicator mice to establish a quantitative high-resolution map of cell cycle kinetics of thymocytes.
View Article and Find Full Text PDFFEBS J
January 2025
Institute of Biomaterials, The First Affiliated Hospital of Ningbo university, China.
The extracellular matrix (ECM) is a network of proteins and other molecules that encase and support cells and tissues in the body. As clinical and biotechnological uses of ECM are expanding, it is essential to assess the environmental impact associated with its production. Due to high levels of customization, various laboratories employ distinct methods; therefore, this study evaluates three common protocols.
View Article and Find Full Text PDFMol Microbiol
January 2025
Laboratório de Biologia Molecular de Patógenos (LBMP), Departamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de São Paulo (Unifesp), São Paulo, Brazil.
Leishmania presents a complex life cycle that involves both invertebrate and vertebrate hosts. By regulating gene expression, protein synthesis, and metabolism, the parasite can adapt to various environmental conditions. This regulation occurs mainly at the post-transcriptional level and may involve epitranscriptomic modifications of RNAs.
View Article and Find Full Text PDFNPJ Precis Oncol
January 2025
Zentalis Pharmaceuticals, Inc., San Diego, CA, USA.
Upregulation of Cyclin E1 and subsequent activation of CDK2 accelerates cell cycle progression from G1 to S phase and is a common oncogenic driver in gynecological malignancies. WEE1 kinase counteracts the effects of Cyclin E1/CDK2 activation by regulating multiple cell cycle checkpoints. Here we characterized the relationship between Cyclin E1/CDK2 activation and sensitivity to the selective WEE1 inhibitor azenosertib.
View Article and Find Full Text PDFNat Commun
January 2025
Department of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Nuclear speckles are membraneless organelles that associate with active transcription sites and participate in post-transcriptional mRNA processing. During the cell cycle, nuclear speckles dissolve following phosphorylation of their protein components. Here, we identify the PP1 family as the phosphatases that counteract kinase-mediated dissolution.
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