Li-ion and Li-S batteries find enormous applications in different fields, such as electric vehicles and portable electronics. A separator is an indispensable part of the battery design, which functions as a physical barrier for the electrode as well as an electrolyte reservoir for ionic transport. The properties of the separators directly influence the performance of the batteries. Traditional polyolefin separators showed low thermal stability, poor wettability toward the electrolyte, and inadequate barrier properties to polysulfides. To improve the performance and durability of Li-ion and Li-S batteries, development of advanced separators is required. In this review, we summarize recent progress on the fabrication and application of novel separators, including the functionalized polyolefin separator, polymeric separator, and ceramic separator, for Li-ion and Li-S batteries. The characteristics, advantages, and limitations of these separators are discussed. A brief outlook for the future directions of the research in the separators is also provided.

Dissolution of different CaO samples into molten synthetic ‘FeO’‐SiO2 and ‘FeO’‐SiO2‐CaO slags was carried out in a closed tube furnace at 1873 K. The slag was kept stagnant. It was found that the dissolution rate was very fast when CaO rod was dipped into ‘FeO’‐SiO2 slag. In the case of ‘FeO’‐SiO2‐CaO slag, the dissolution of CaO rod in the stagnant slag was retarded after the initial period (2 minutes). Only less than 16 percent CaO reacted with the slag, irrespective of the type of lime. Three phase‐regions were identified in the reacted part of the lime rod by SEM‐EDS analysis. The formation of these regions was explained thermodynamically. A dense layer of 2CaO · SiO2 was found to be responsible for the total stop of the dissolution. It could be concluded that constant removal of the 2CaO · SiO2 layer would be of essence to obtain a high dissolution rate of lime. In this connection, it was found necessary to study the dissolution of lime in moving slag to reach a reliable conclusion regarding the relevance of the reactivity obtained by water ATSM test to the real reactivity of lime in high temperature slag.

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The applicability of rotating rod technique in the study of lime dissolution in slag was investigated. Both computational fluid dynamic (CFD) and cold model experiments showed that the mass transfer due to radial velocity introduced by forced convection was zero if the rod was long. The mass transfer by forced convection was also less important in comparison with natural convection and diffusion when the rod was half length of the height of the bath. This finding was in accordance with the criteria put forward by the original work that the method could only be applicable when a thin disk (instead of rod) with big diameter and big liquid bath were used. To study the lime dissolution by forced convection a new experimental technique was developed. A cube was placed in the slag that was eccentrically stirred. The whole system, viz. the sample along with the slag could be quenched. The new technique could study the effect of forced convection on the dissolution. The microscopic study on the quenched slag-lime samples could reveal the dissolution mechanism successfully.

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