ABSTRACT
Despite their potential in heating supply systems, thus far high-temperature aquifer thermal energy storages (HT-ATES) currently lack widespread application. Reducing the potential risks by improving the predictability of hydrogeochemical processes accelerated or initiated at elevated temperatures might promote the development of this technology. Therefore, we report the results of a short-term hot water infiltration field test with subsurface temperatures above 70 °C, along with associated laboratory batch tests at 10, 40 and 70 °C for 28 sediment samples to determine their usability for geochemical prediction. Most groundwater components had lower maximal concentrations and smaller concentration ranges in field samples compared to the batch tests. This indicates that the strongest geochemical effects observed in laboratory tests with sufficient site-specific sediment samples will likely be attenuated at the field scale. A comparison of field measurements with predicted concentration ranges, based on temperature induced relative concentration changes from the batch tests, revealed that the predictive power was greatest, where the hot infiltrated water had cooled least and the strongest geochemical effects occurred. The batch test-based predictions showed the best accordance with field data for components, with significant temperature-induced concentration changes related to ion exchange and (de)sorption processes. However, accurate prediction of concentration changes based on other processes, e.g. mineral dissolution, and downstream reversals in concentrations, requires further investigation. The here presented procedure enables the prediction of maximal expectable temperature-dependant concentration changes for most environmentally relevant ancillary groundwater components, e.g. As, with limited effort.
ABSTRACT
This document compiles the data related to a high temperature heat injection test, which was carried out at an injection temperature of 74 °C in a shallow aquifer and is presented by Heldt et al. [1]. The data set contains transient measurements of temperatures at 18 wells in 10 depths and measurements of the experimental boundary conditions (injection temperature and flow rate) at a temporal resolution of up to 1 min. The spatial configuration and the technical details about where and how the data have been measured are provided. In addition, data of a multilevel multi well pumping test are shown. The presented data is useful to gain insights into the thermohydraulic processes induced by a high temperature heat injection test and can furthermore be used for the development and verification of numerical models of the presented experiment and similar applications like high temperature aquifer thermal energy storage.
ABSTRACT
A quantitative real-time reverse transcriptase PCR (RT-qPCR) assay was developed for the analysis of influenza A virus transcription and replication dynamics in mammalian cell culture. The assay is based on a polarity- and sequence-specific reverse transcription used to distinguish specifically between viral genomes (vRNA(-)), replicative intermediates (cRNA(+)) and viral messenger RNAs (vmRNA(+)) of segments 4 (HA), 6 (NA), 7 (M) and 8 (NS) during the life cycle of influenza virus. Synthetic viral RNAs used as reference standards for validation and quantitation were prepared for each viral RNA type and segment. Assay validation demonstrated linearity over five orders of magnitude, sensitivity of 1.0 x 10(3) to 8.9 x 10(3) of viral RNA molecules, repeatability and reproducibility of less than 0.8-3.1% CV (coefficient of variation). Dynamics of influenza A virus infection in adherent MDCK cells, a substrate considered for human influenza vaccine manufacturing, were analyzed. In general, mainly vmRNA(+) were synthesized during early phases of infection at about 0.6 hpi, followed immediately by cRNA(+) synthesis and after a short delay of about 1.9 hpi viral genome replication could be detected. The vRNA(-)s were synthesized in equimolar amounts and similar dynamics whereas preferential synthesis of NS1 vmRNA(+) in early transcription phases and a delay for M1 vmRNA(+) was found.
