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Ethylene glycol nanofluids dispersed with monolayer graphene oxide nanosheet for high-performance subzero cold thermal energy storage.

ABSTRACT: Ethylene glycol (EG) nanofluids have been intensively explored as one of the most promising solid-liquid phase change materials for subzero cold thermal energy storage (CTES). However, the prepared nanofluids usually suffer from a large supercooling degree, a long freezing period, reduced storage capacity and poor dispersion stability. Herein, we overcome these issues by developing stable EG nanofluids that are uniformly dispersed with low concentrations of monolayer ethanol-wetted graphene oxide nanosheets. The homogeneously dispersed monolayer sheet not only improves the thermal conductivity of the nanofluids (12.1%) but also provides the heterogeneous nucleation sites to trigger the crystal formation, thereby shortening the freezing time and reducing the supercooling degree. Compared with the base fluid, the nanofluids have reduced the supercooling degree by 87.2%, shortened the freezing time by 78.2% and maintained 98.5% of the latent heat. Moreover, the EG nanofluids have retained their initial stable homogeneous dispersion after repeated freezing/melting for 50 cycles, which ensures consistent CTES behavior during long-period operations. The facile preparation process, low loading requirement and consistent superior thermophysical properties would make the EG nanofluids loaded with monolayer graphene oxide sheets promising coolants for high-performance phase change-based CTES.

SUBMITTER: Zhang J

PROVIDER: S-EPMC9041135 | biostudies-literature | 2021 Sep

REPOSITORIES: biostudies-literature

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Ethylene glycol nanofluids dispersed with monolayer graphene oxide nanosheet for high-performance subzero cold thermal energy storage.

Zhang Jingyi J Fu Benwei B Song Chengyi C Shang Wen W Tao Peng P Deng Tao T

RSC advances 20210914 49

Ethylene glycol (EG) nanofluids have been intensively explored as one of the most promising solid-liquid phase change materials for subzero cold thermal energy storage (CTES). However, the prepared nanofluids usually suffer from a large supercooling degree, a long freezing period, reduced storage capacity and poor dispersion stability. Herein, we overcome these issues by developing stable EG nanofluids that are uniformly dispersed with low concentrations of monolayer ethanol-wetted graphene oxid ...[more]

PMID: 35479859

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Project description:Developing stable nanofluids and improving their thermo-physical properties are highly important in heat transfer applications. In the present work, the stability, thermal conductivity, and rheological properties of tungsten disulphide (WS2) nanoparticles (NPs) with ethylene glycol (EG) were profoundly examined using a particle size analyzer, zeta-sizer, thermal property analyzer, rheometer, and pH measuring system. WS2 NPs were characterized by various techniques, such as XRD (X-Ray Diffraction), FTIR (Fourier Transform Infrared Spectroscopy), FESEM (Field emission scanning electron microscopy), and high-resolution transmission electron microscopy (HRTEM). The nanofluids were obtained with the two-step method by employing three volume concentrations (0.005%, 0.01%, and 0.02%) of WS2. The influence of different surfactants (Sodium dodecyl sulphate (SDS), Sodium dodecylbenzenesulfonate (SDBS), Cetyltrimethylammonium bromide (CTAB)) with various volume concentrations (0.05-2%) on the measured properties has also been evaluated. Pristine WS2/EG nanofluids exhibit low zeta potential values, i.e., -7.9 mV, -9.3 mV, and -5 mV, corresponding to 0.005%, 0.01%, and 0.02% nanofluid, respectively. However, the zeta potential surpassed the threshold (±30 mV) and the maximum values reached of -52 mV, -45 mV, and 42 mV for SDS, SDBS, and CTAB-containing nanofluids. This showed the successful adsorption of surfactants onto WS2, which was also observed through the increased agglomerate size of up to 1720 nm. Concurrently, particularly for 0.05% SDS with 0.005% WS2, thermal conductivity was enhanced by up to 4.5%, with a corresponding decrease in viscosity of up to 10.5% in a temperature range of (25-70 °C), as compared to EG. Conversely, the viscoelastic analysis has indicated considerable yield stress due to the presence of surfactants, while the pristine nanofluids exhibited enhanced fluidity over the entire tested deformation range. The shear flow behavior showed a transition from a non-Newtonian to a Newtonian fluid at a low shear rate of 10 s-1. Besides this, the temperature sweep analysis has shown a viscosity reduction in a range of temperatures (25-70 °C), with an indication of a critical temperature limit. However, owing to an anomalous reduction in the dynamic viscosity of up to 10.5% and an enhancement in the thermal conductivity of up to 6.9%, WS2/EG nanofluids could be considered as a potential candidate for heat transfer applications.

Project description:The crystallinity of polymers strongly affects their properties. For block copolymers, whereby two crystallisable blocks are covalently tethered to one another, the molecular weight of the individual blocks and their relative weight fraction are important structural parameters that control their crystallisation. In the case of block copolymer micelles, these parameters can influence the crystallinity of the core, which has implications for drug encapsulation and release. Therefore, in this study, we aimed to determine how the microstructure of poly(ethylene glycol-b-caprolactone) (PEG-b-PCL) copolymers contributes to the crystallinity of their hydrophobic PCL micelle cores. Using a library of PEG-b-PCL copolymers with PEG number-average molecular weight (Mn) values of 2, 5, and 10 kDa and weight fractions of PCL (fPCL) ranging from 0.11 to 0.67, the thermal behaviour and morphology were studied in blends, bulk, and micelles using differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WXRD), and Synchrotron wide-angle X-ray scattering (WAXS). Compared to PEG and PCL homopolymers, the block copolymers displayed reduced crystallinity in the bulk phase and the individual blocks had a large influence on the crystallisation of one another. The fPCL was determined to be the dominant contributor to the extent and order of crystallisation of the two blocks. When fPCL < 0.35, the initial crystallisation of PEG led to an amorphous PCL phase. At fPCL values between 0.35 and 0.65, PEG crystallisation was followed by PCL crystallisation, whereas this behaviour was reversed when fPCL > 0.65. For lyophilised PEG-b-PCL micelles, the crystallinity of the core increased with increasing fPCL, although the core was predominately amorphous for micelles with fPCL < 0.35. These findings contribute to understanding the relationships between copolymer microstructure and micelle core crystallinity that are important for the design and performance of micellar drug delivery systems, and the broader application of polymer micelles.

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Ethylene glycol nanofluids dispersed with monolayer graphene oxide nanosheet for high-performance subzero cold thermal energy storage.

Publications

Ethylene glycol nanofluids dispersed with monolayer graphene oxide nanosheet for high-performance subzero cold thermal energy storage.

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