The current state of hydrochemical indicators of Lake Kenon– the cooling reservoir of the TPP

A characteristic is given of the current hydrochemical state of the water of Lake Kenon, which is used as a reservoir - a cooler for the Chita TPP. For over 50-years of operation of the station located on its shore, under the conditions of anthropogenic impact, there has been a sharp change in the chemical type of the lakeʼs water. Currently, the predominant anion is the sulfate ion. Above the MPC standard for water of water bodies of fishery significance are the content of magnesium and sulfates and the trace elements: fluorine, vanadium, strontium, molybdenum, copper, tungsten. The concentrations of boron, lithium, bromine are relatively increased, in some samples - iron, manganese, aluminum and barium.

A Chemical-Transport-Mechanics Numerical Model for Concrete under Sulfate Attack

Sulfate attack is one of the crucial causes for the structural performance degradation of reinforced concrete infrastructures. Herein, a comprehensive multiphase mesoscopic numerical model is proposed to systematically study the chemical reaction-diffusion-mechanical mechanism of concrete under sulfate attack. Unlike existing models, the leaching of solid-phase calcium and the dissolution of solid-phase aluminate are modeled simultaneously in the developed model by introducing dissolution equilibrium equations. Additionally, a calibrated time-dependent model of sulfate concentration is suggested as the boundary condition. The reliability of the proposed model is verified by the third-party experiments from multiple perspectives. Further investigations reveal that the sulfate attack ability is underestimated if the solid-phase calcium leaching is ignored, and the concrete expansion rate is overestimated if the dissolution of solid-phase aluminate is not modeled in the simulation. More importantly, the sulfate attack ability and the concrete expansion rate is overestimated if the time-dependent boundary of sulfate concentration is not taken into consideration. Besides, the sulfate ion diffusion trajectories validate the promoting effect of interface transition zone on the sulfate ion diffusion. The research of this paper provides a theoretical support for the durability design of concrete under sulfate attack.

Trilobites, Biostratigraphy, and Geochemistry of the Middle Cambrian Kuonamka Formation (Northeastern Siberian Platform, Kyulenke River)

—We studied the middle Cambrian unit of the Kuonamka Formation section on the Kyulenke River (Siberian Platform) and performed its biostratigraphic subdivision based on trilobites. The middle Cambrian section has intervals corresponding to the regional zones of the Amginian Stage. Six levels with mass accumulation of fauna remains have been identified: Two levels are located within the Ovatoryctocara Zone; the third level is at the boundary between the Ovatoryctocara and Kounamkites zones; the fourth layer is confined to the roof of the Triplagnostus gibbus Zone; and the fifth and sixth levels are located within the Tomagnostus fissus–Paradoxides sacheri Zone. The composition of rocks and bitumens of their organic matter (OM) has been studied, including the geochemical specifics of the mineral components of rocks (iron, sulfur, and CO2) and of saturated hydrocarbons of bitumens as well as noncarbonate carbon isotopes in the OM. It has been established that the OM sedimentation took place under normal aeration of the sea basin waters, without hydrogen sulfide contamination of the bottom waters. The intensity of chemical and biochemical transformations of mineral and organic components during diagenesis was controlled by the contents of organic carbon and sulfate ion, the activity of the anaerobic prokaryote community, and the rate of sediment mineralization. We have also established relationships between the content of organic carbon in potentially oil source rocks and the contents of iron oxide, total sulfur, and sulfide and sulfate sulfur as well as the ratios of saturated hydrocarbons. The alternation of highly carbonaceous black shales and carbonaceous rocks is apparently due to a change in the composition of biologic communities of microorganisms (sources of hydrocarbon biomarkers) and in the intensity of OM transformation during diagenesis. We assume that the OM transformation included sulfate reduction and dealkylation of high-molecular steroids in the unconsolidated OM-enriched marine sediments with the participation of bacteria. The intensity of these processes depended on the mass of the primary OM, the amount of sulfate ion, and, hence, the pH and Eh of the medium.

Effects of Sodium Sulfate Attack on Concrete Incorporated with Drying-Wetting Cycles

It has been widely observed that sulfate attack can damage the durability of concrete. This research investigated the mass loss and damage degree of concrete under sodium sulfate attack incorporated with drying-wetting cycles. The impact factors, including water-binder ratio, solution concentration of sodium sulfate, fly ash content, curing time, and drying-wetting cycle system, were observed to influence the sodium sulfate attack by the mass loss rate and damage degree at regular time intervals. Also, the hydrates of sulfate-attacked samples were analyzed using X-ray diffraction. Results indicated that a high water-binder and high-concentration sodium sulfate solution could accelerate the transportation of sulfate ion inside the concrete and the deterioration degree of concrete. Appropriate fly ash and longer curing time can effectively improve the internal pore structure of concrete to reduce the sulfate corrosion damage. The sulfate ion erosion and deterioration degree of the concrete are synchronously intensified along with the increase of the baking-immersing time ratio. The trend of the predicted life for concrete is basically consistent with the damage evolution result, indicating the feasibility of the Weibull distribution model to predict the service life of concrete under sodium sulfate attack incorporated with drying-wetting cycles.

Structural Study and Antibacterial Activity of Cetylpyridinium Dodecyl Sulfate Ion Pair

A bactericidal and structural study on the cetylpyridinium dodecyl sulfate ion pair has been taken. The ion pair was a subject of numerous investigations, and its properties are widely discussed in different works. However, systematic studies on the specific interionic interactions in this ion pair are absent in the literature. To fill the gap in knowledge on the structure of cetylpyridinium dodecyl sulfate, we have synthesized this ion pair and characterized it with XRD, NMR, and DFT techniques. Moreover, antibacterial activity against various bacteria strains was analyzed.