The present research work aimed to investigate the melting and solidification characteristics of NPCM. The NPCM was prepared using paraffin as the PCM and high conductive MWCNT as the nanomaterial without using any dispersant. The NPCM was prepared by dispersing MWCNTs with volume fractions of 0.3%, 0.6% and 0.9% in PCM as the base PCM. SEM morphology showed the uniform dispersion of MWCNTs in the paraffin wax. The MWCNT nano-additives PCMs showed two peaks in the heating curve by DSC measurement. Lessening in melting and solidification time of 30% and 43% was attained in the case of NPCM with 0.3% and 0.9%, respectively. It is observed from the DSC analysis that the latent heat of pure paraffin during freezing and melting cycle was 139.2 J/g (at 56.61 °C) and 131.8 J/g (at 57.55 °C), respectively. Whereas, the latent heat of NPCM with 0.9% of nanofluid was 150.7 J/g (at 56.36 °C) and 148.3 J/g (58.35 °C). It is construed that a maximum change in latent heat of 7.6% and 11% was observed between pure PCM and NPCM during freezing and melting cycle. For the lesser nanoparticle concentration (0.3% and 0.6%), the percentage change in latent heat was lesser than 0.9%. 相似文献
In this paper a new mathematical model of secondary frost heave is presented. It isexpected that the problem considered under some assumptions is well-posed. 相似文献
Post‐crystallization treatments such as manual fishing of crystals and soaking in cryoprotectant solutions, especially of large macromolecular complexes and membrane proteins, are cumbersome and often lead to crystal damage and reduced diffraction data quality. Here, a capillary crystallization plate is presented that simultaneously allows counter‐diffusion crystallization at the nanolitre scale in a high‐throughput screening mode, low‐temperature in situ diffraction data collection from crystals after cryoprotection and low‐temperature in situ data collection of crystals without the addition of any cryoprotectant after high‐pressure (HP) freezing. The development of this plate and plunge cooling of crystals in the capillaries is a major step towards implementing automated in situ high‐throughput crystal diffraction data collection at a synchrotron beamline. In combination with HP freezing this offers a new opportunity to obtain structural information from fragile crystals of supramolecular complexes that might otherwise not be feasible. 相似文献
Hydrogels for this study were prepared from a mixture of PVA and CMC using three different techniques, i.e., freezing and thawing, electron‐beam irradiation or combined freezing and thawing and electron beam irradiation. A comparative study between the three techniques was carried out in terms of gel fraction (%) and swelling (%). It was found that the physical properties of the hydrogel were improved when the combination of freezing and thawing and irradiation were used rather than just freezing and thawing, or irradiation only. The effects of temperature and soil fertilizers on swelling (%) were examined to evaluate the usefulness of the hydrogel as a super absorbent in the soil. It was found that the swelling ratio increased as the composition of CMC increased in the blend. Hence, the blend having the composition 80/20 (CMC/PVA) was used as a super absorbent in the soil for agriculture. Moreover, the water retention increased in the soil containing this hydrogel. Thus, this type of hydrogel can be used to increase water retention in desert regions. 相似文献
Heat‐shrink tubing, which shrinks in one plane only (its diameter) when heated, commonly used for sealing protection in electrical engineering, was found to be able to function as a solid‐phase microextraction coating. Its utility was demonstrated for the determination of phthalic acid esters in an aqueous solution combined with high‐performance liquid chromatography equipped with a UV absorbance detector. The preparation procedure was rather simple and only ～10 min was needed. The fiber cost is extremely low (～10 cent each). The parameters affecting the extraction were optimized. Heat‐shrink tubing fiber exhibited a significant enrichment effect for the three examined phthalic acid esters and up to 931‐fold enrichment factor was obtained. The limit of detection was <10 μg/L for all analytes. The operation repeatability and fiber‐to‐fiber reproducibility were 1.2–8.3 and 5.4–9.1%, respectively. It was successfully applied for the analysis of bottled drinking water with recoveries ranging from 90.1–100.5%. 相似文献
This study introduces a preparation method for polymer‐encased monolith frits with improved durability for liquid chromatography columns. The inner surface of the polyether ether ketone tubing is pretreated with sulfuric acid in the presence of catalysts (vanadium oxide and sodium sulfate). The tubing was rinsed with water and acetone, flushed with nitrogen, and treated with glycidyl methacrylate. After washing, the monolith reaction mixture composed of lauryl methacrylate, ethylene glycol dimethacrylate, initiator, and porogenic solvent was filled in the tubing and subjected to in situ polymerization. The tubing was cut into thin slices and used as frits for microcolumns. To check their durability, the frit slices were placed in a vial and a heavy impact was applied on the vial by a vortex mixer for various periods. The frits made in the presence of catalysts were found to be more durable than those made without catalysts. Furthermore, when the monolith‐incorporated tubing was used as a chromatography column, the column prepared in the presence of catalysts resulted in a better separation efficiency. The separation performance of the columns installed with the polyether ether ketone encased monolith frits was comparable to that of the columns installed with the commercial stainless‐steel screen frits. 相似文献
Summary: A novel experimental approach based on the freezing‐point depression of a solvent in a swollen gel has been developed to characterize the structure of nanocomposites. A higher depression in the freezing point has been related with an exfoliated nanocomposite. This increased depression not only depends on the formation of a tighter network but also on the decrease of the size of the solvent cages where the nucleation takes place.
The nucleation process of unfilled and organoclay‐filled natural rubber with the same crosslinking density. 相似文献
