Vermiculite bio-barriers for Cu and Zn remediation: an eco-friendly approach for freshwater and sediments protection

The increase in heavy metal contamination in freshwater systems causes serious environmental problems in most industrialized countries, and the effort to find eco-friendly techniques for reducing water and sediment contamination is fundamental for environmental protection. Permeable barriers made of natural clays can be used as low-cost and eco-friendly materials for adsorbing heavy metals from water solution and thus reducing the sediment contamination. This study discusses the application of permeable barriers made of vermiculite clay for heavy metals remediation at the interface between water and sediments and investigates the possibility to increase their efficiency by loading the vermiculite surface with a microbial biofilm of Pseudomonas putida, which is well known to be a heavy metal accumulator. Some batch assays were performed to verify the uptake capacity of two systems and their adsorption kinetics, and the results indicated that the vermiculite bio-barrier system had a higher removal capacity than the vermiculite barrier (+34.4 and 22.8 % for Cu and Zn, respectively). Moreover, the presence of P. putida biofilm strongly contributed to fasten the kinetics of metals adsorption onto vermiculite sheets. In open-system conditions, the presence of a vermiculite barrier at the interface between water and sediment could reduce the sediment contamination up to 20 and 23 % for Cu and Zn, respectively, highlighting the efficiency of these eco-friendly materials for environmental applications. Nevertheless, the contribution of microbial biofilm in open-system setup should be optimized, and some important considerations about biofilm attachment in a continuous-flow system have been discussed.     

Mechanisms of partly flooded loose sand deposits

Partly flooded loose sand deposits are left back from lignite mining, particularly in east Germany. After flooding, gas inclusions in macropores enhance the pore pressure increase by total stress cycles without drainage, and this can cause the transition into a kind of suspension. Thus, natural and technical changes of surface loads triggered flow slides in chain reactions of sometimes catastrophic extent. Such collapsible deposits were and are stabilized by blast-induced liquefaction and densification. Successive collapse fronts in flooded grain skeletons are seismogeneous, and this appears as wavering in the near-field and leads to power-law spectra in the far-field. Apart from this evidence of mild fractality, the wild fractality of chain reactions eludes mathematical treatment. Therefore, uncommon methods of geotechnical design, operations and monitoring are required.     

Low-Titanium Lamproites of the Ryabinoviy Massif (Aldan Shield): Crystallization Conditions and Lithospheric Source

Obtained data shows that high-potassic dyke rocks of the Ryabinoviy massif (Central Aldan) belong to low-titanium lamproite series (Mediterranean type) and are distinct with “classic” high-titanium lamproites. Based on Al-in-olivine thermometer, temperature of olivine–chrome-spinel pair crystallization varies in range between 1100 and 1250°C. This suggests lithospheric mantle source for the parental melt and makes role of mantle plume insignificant. High-precision data on olivine composition and bulk rock traceelement composition imply mixed source for the parental melt, consisted of depleted peridotite and enriched domains, originated during ancient subduction.     

Formation of Water-Bearing Defects in Olivine in the Presence of Water–Hydrocarbon Fluid at 6.3 GPa and 1200°C

The main trends of water dissolution in Fe-bearing olivine have been investigated in the olivine–H₂O–hydrocarbon fluid system in experiments at a pressure of 6.3 GPa, a temperature of 1200°C, and hydrogen fugacity ( fH₂) buffered by the Mo–MoO₂ equilibrium. The content and contribution of ОH defects of different types in Fe-bearing olivines depend on the composition of reduced fluids in the system. As the fraction of hydrocarbons in the fluid increases, the H₂O content in olivine crystals decreases from 900 to 160–180 ppm, while the ОН absorption peaks become lower at high frequencies and occupy a larger part of the infrared spectrum in the low-frequency region. According to the experimental results, even the deepest seated mantle olivines with OH defects were not equilibrated with a fluid rich in light alkanes or oxygenated hydrocarbons.