Dataset Information

Accelerated Thermal Cycling Test of Microencapsulated Paraffin Wax/Polyaniline Made by Simple Preparation Method for Solar Thermal Energy Storage.

ABSTRACT: Microencapsulated paraffin wax/polyaniline was prepared using a simple in situ polymerization technique, and its performance characteristics were investigated. Weight losses of samples were determined by Thermal Gravimetry Analysis (TGA). The microencapsulated samples with 23% and 49% paraffin showed less decomposition after 330 °C than with higher percentage of paraffin. These samples were then subjected to a thermal cycling test. Thermal properties of microencapsulated paraffin wax were evaluated by Differential Scanning Calorimeter (DSC). Structure stability and compatibility of core and coating materials were also tested by Fourier transform infrared spectrophotometer (FTIR), and the surface morphology of the samples are shown by Field Emission Scanning Electron Microscopy (FESEM). It has been found that the microencapsulated paraffin waxes show little change in the latent heat of fusion and melting temperature after one thousand thermal recycles. Besides, the chemical characteristics and structural profile remained constant after one thousand thermal cycling tests. Therefore, microencapsulated paraffin wax/polyaniline is a stable material that can be used for thermal energy storage systems.

SUBMITTER: Silakhori M

PROVIDER: S-EPMC5452494 | biostudies-other | 2013 Apr

REPOSITORIES: biostudies-other

ACCESS DATA

Similar Datasets

Project description:Seasonal heat storage is considered as one of the key elements on the path to a low-emission economy. Embedded in local district heating networks, they raise the share of renewable energies and balance out highly fluctuating supplies of e.g. solar systems or windmills. The technology of seasonal heat storage can be described as almost technically mature, with well-established concepts and some systems being in operation for a considerable time. Nevertheless, the operating experience gained to date also revealed two critical problems. On the one hand, even smallest leakages in sealing foils led to irreparable breakdowns. On the other hand, heat loss in the marginal areas was revealed as a key deficiency, preventing the technology from advancing towards global marketability. This study presents an experimental approach to address these two key issues in the field of seasonal energy storage. Two small-scale laboratory tests were carried out to test paraffin wax as a completely novel component in the marginal area of seasonal storages. This is based on two material properties: As hydrophobic and mobile medium, the warmed and molten paraffin should actively seal the fissures and holes in the event of leakage. Additionally, the latent heat storage properties of the paraffin wax should increase the systems' total storage capacity and reduce lateral heat losses via its low thermal conductivity. With retardation periods from 2.5 to 4 hours, the results show an effective phase change effect of the paraffin wax, which reduces energy losses and allows to buffer short-term, intensive loading and unloading processes. By storing up to 138 kJ/kg energy in the paraffin wax, increased capacities of application-scale pit storages by up to 40.70 MWh are to be expected. Additionally, the self-healing features could be successfully demonstrated: With only small losses of between 1.5 and 17%, the paraffin wax effectively sealed artificially incised leaks. Thereby, the mechanism was most effective for local defects. Following these positive demonstrations of feasibility, technical design questions still remain, which concern prevention of deformation of the paraffin wax. Once solved, this new component can then provide a path for further optimization of seasonal heat storage technologies.

Project description:Molecular photoswitches that are capable of storing solar energy, so-called molecular solar thermal storage systems, are interesting candidates for future renewable energy applications. In this context, substituted norbornadiene-quadricyclane systems have received renewed interest due to recent advances in their synthesis. The optical, thermodynamic, and kinetic properties of these systems can vary dramatically depending on the chosen substituents. The molecular design of optimal compounds therefore requires a detailed understanding of the effect of individual substituents as well as their interplay. Here, we model absorption spectra, potential energy storage, and thermal barriers for back-conversion of several substituted systems using both single-reference (density functional theory using PBE, B3LYP, CAM-B3LYP, M06, M06-2x, and M06-L functionals as well as MP2 calculations) and multireference methods (complete active space techniques). Already the diaryl substituted compound displays a strong red-shift compared to the unsubstituted system, which is shown to result from the extension of the conjugated ?-system upon substitution. Using specific donor/acceptor groups gives rise to a further albeit relatively smaller red-shift. The calculated storage energy is found to be rather insensitive to the specific substituents, although solvent effects are likely to be important and require further study. The barrier for thermal back-conversion exhibits strong multireference character and as a result is noticeably correlated with the red-shift. Two possible reaction paths for the thermal back-conversion of diaryl substituted quadricyclane are identified and it is shown that among the compounds considered the path via the acceptor side is systematically favored. Finally, the present study establishes the basis for high-throughput screening of norbornadiene-quadricyclane compounds as it provides guidelines for the level of accuracy that can be expected for key properties from several different techniques.

Dataset Information

Accelerated Thermal Cycling Test of Microencapsulated Paraffin Wax/Polyaniline Made by Simple Preparation Method for Solar Thermal Energy Storage.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets