Some properties of A sedimentary laterite soil as engineering construction material

A sedimentary laterite soil is examined for its suitability as a construction material by the consideration of its mineralogy and basic geotechnical properties as well as its consolidation and permeability in the compacted state. Three compaction energy levels are utilised. Mineralogically, the soil contains virtually nothing undesirable while its basic geotechnical properties are those generally ascribed to non-problematic soils. The compressibility of the soil varies from moderate to low depending on the energy of compaction. It is however impervious for all the compaction energy levels. The sedimentary laterite soil constitute a good engineering construction material as it has already been successfully used as base and sub-base material in road construction. Results obtained in this study show that this laterite soil is also suitable for use as fill materials in embankment and dam construction.     

Laboruntersuchungen zur Freisetzung von Unat aus einem Gestein unter oxischen naturnahen Bedingungen

Kurzfassung Im Labor wurden verschiedene Größen (pH-Wert, HCO ₃ —Gehalt, Präsenz von Fe(OH) ₃ ) untersucht, von denen angenommen werden konnte, dass sie die umweltrelevante Freisetzung von Uran aus Gesteinen (z. B. Haufwerken, Halden, Tailings) im neutralen und schwach basischen pH-Bereich (6 bis 9) beeinflussen. Hierzu wurde der Austrag von U _nat aus einem schwach vererzten Urangestein (2,31 %) in Batchversuchen untersucht. Diese Versuche wurden mit 8, 10 oder 40 g/l Gestein und Leitungs- bzw. Mineralwasser durchgeführt. Zum Vergleich wurden parallele Standversuche in deionisiertem Wasser, 0,1 M Na ₂ CO ₃ und 0,1 M H ₂ SO ₄ durchgeführt. Die Ergebnisse zeigen eine Begünstigung der Uranfreisetzung in Anwesenheit von Carbonat (gelöst oder in situ durch Dolomitauflösung entstanden), während die Rolle des Pyrits auf die Freisetzung deutlich komplexer ist. Das Erreichen eines Gleichgewichtszustands kann unter Umständen durch sorptive Einflüsse verzögert werden.

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Investigations for the release of U_nat from ore bearing rock under natural near oxic conditions

Abstract The effects of carbonate concentration and the presence of iron hydroxide phases on uranium release into the environment were investigated under oxic conditions and in the pH range from 6 to 9. For this purpose not-shaken batch experiments were conducted with a constant amount (8, 10 or 40 g/l) of a uranium bearing rock and different types of water (deionised, tap and mineral water). For comparison parallel experiments were conducted with 0.1 M Na ₂ CO ₃ and 0.1 M H ₂ SO ₄ . The use of dolomite confirmed the favourable role of carbonate bearing minerals for U transport while the presence of pyrite on Uranium mobilisation was shown to be considerably more complex. This study shows that the approach of equilibrium conditions can be strongly delayed by sorption processes.

     

Comparative Cytotoxicity of Artemisinin and Cisplatin and Their Interactions with Chlorogenic Acids in MCF7 Breast Cancer Cells

In parts of Africa and Asia, self‐medication with a hot water infusion of Artemisia annua (Artemisia tea) is a common practice for a number of ailments including malaria and cancer. In our earlier work, such an extract showed better potency than artemisinin alone against both chloroquine‐sensitive and ‐resistant parasites. In this study, in vitro tests of the infusion in MCF7 cells showed high IC₅₀ values (>200 μM ). The combination of artemisinin and 3‐caffeoylquinic acid (3CA), two major components in the extract, was strongly antagonistic and gave a near total loss of cytotoxicity for artemisinin. We observed that the interaction of 3CAs with another cytotoxic compound, cisplatin, showed potentiation of activity by 2.5‐fold. The chelation of cellular iron by 3CA is hypothesized as a possible explanation for the loss of artemisinin activity.     

Linear Aliphatic Dialkynes as Alternative Linkers for Double‐Click Stapling of p53‐Derived Peptides

We investigated linear aliphatic dialkynes as a new structural class of i,i+7 linkers for the double‐click stapling of p53‐based peptides. The optimal combination of azido amino acids and dialkynyl linker length for MDM2 binding was determined. In a direct comparison between aliphatic and aromatic staple scaffolds, the aliphatic staples resulted in superior binding to MDM2 in vitro and superior p53‐activating capability in cells when using a diazidopeptide derived from phage display. This work demonstrates that the nature of the staple scaffold is an important factor that can affect peptide bioactivity in cells.