Hydrothermal liquefaction is one of the common thermochemical conversion methods adapted to convert high-water content biomass feedstocks to biofuels and many other valuable industrial chemicals. The hydrothermal process is broadly classified into carbonization, liquefaction, and gasification with hydrothermal liquefaction conducted in the intermediate temperature range of 250–374 °C and pressure of 4–25 MPa. Due to the ease of adaptability, there has been considerable research into the process on using various types of biomass feedstocks. Over the years, various solvents and co-solvents have been used as mediums of conversion, to promote easy decomposition of the lignocellulosic components in biomass. The product separation process, to obtain the final products, typically involves multiple extraction and evaporation steps, which greatly depend on the type of extractive solvents and process parameters. In general, the main aim of the hydrothermal process is to produce a primary product, such as bio-oil, biochar, gases, or industrial chemicals, such as adhesives, benzene, toluene, and xylene. All of the secondary products become part of the side streams. The optimum process parameters are obtained to improve the yield and quality of the primary products. A great deal of the process depends on understanding the underlined reaction chemistry during the process. Therefore, this article reviews the major works conducted in the field of hydrothermal liquefaction in order to understand the mechanism of lignocellulosic conversion, describing the concept of a batch and a continuous process with the most recent state-of-art technologies in the field. Further, the article provides detailed insight into the effects of various process parameters, co-solvents, and extraction solvents, and their effects on the products’ yield and quality. It also provides information about possible applications of products obtained through liquefaction. Lastly, it addresses gaps in research and provides suggestions for future studies.

The technical feasibility of underground coal gasification (UCG) has been established through many field trials and laboratory-scale experiments over the past decades. However, the UCG is site specific and the commercialization of UCG is being hindered due to the lack of complete information for a specific site of operation. Since conducting UCG trials and data extraction are costly and difficult, modeling has been an important part of UCG study to predict the effect of various physical and operating parameters on the performance of the process. Over the years, various models have been developed in order to improve the understanding of the UCG process. This article reviews the approaches, key concepts, assumptions, and limitations of various forward gasification UCG models for cavity growth and product gas recovery. However, emphasis is given to the most important models, such as packed bed models, the channel model, and the coal slab model. In addition, because of the integral part of the main models, various sub-models such as drying and pyrolysis are also included in this review. The aim of this study is to provide an overview of the various simulation methodologies and sub-models in order to enhance the understanding of the critical aspects of the UCG process.