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Since the 1990s, supercritical fluids for the synthesis of nanomaterials have been paid more and more attention by researchers and have gradually become one of the most important ways to prepare nanomaterials. In this study, literature data on "supercritical fluids for the synthesis of nanomaterials" from 1998 to 2020 were obtained from the Web of Science database, and the data were processed and analyzed by the bibliometric method combined with Microsoft office 2019, Origin 2018, VOSviewer, and other software, so as to obtain the research status and development trend of "supercritical fluids for the synthesis of nanomaterials". The results show that since literature on "supercritical fluids for the synthesis of nanomaterials" appeared for the first time in 1998, the number of articles published every year has risen. In terms of this field, China has become the second-largest publishing country after the United States, and China and the United States display a lot of cooperation and exchanges in this field. "Supercritical CO2", "supercritical water", "supercritical antisolvent", "surface modification", and so on have become the research hotspots of "supercritical fluids for the synthesis of nanomaterials". [ABSTRACT FROM AUTHOR]

The high moisture content and heavy metal concentration of hyperaccumulator are the main bottlenecks of resource utilization. Supercritical water gasification technology was used to convert Sedum plumbizincicola (a hyperaccumulator of Zn and Cd) into hydrogen gas and to immobilize HMs into biochar. Homogeneous alkali metal catalysts such as NaOH, Na 2 CO 3 and Ca(OH) 2 were added to optimize the experimental conditions. The results showed that NaOH was effective in capturing CO 2 in-situ , thereby shifting the water-gas shift reaction equilibrium in the forward direction. And the increase of NaOH concentration had a significant promotion effect on hydrogen production. In the non-catalytic gasification of Sedum plumbizincicola , the highest hydrogen (1.5 mol/kg) and H 2 selectivity (22.9%) with greater carbon gasification efficiency (19.3%) and lower H 2 gasification efficiency (8.7%) of the gas products were obtained at 400 °C with 6 wt% material concentration for 20 min. However, NaOH at 5% mass fraction maximized hydrogen and H 2 selectivity up to 7.5 and 98.2%, respectively. Alkali catalyst not only promoted the generation of hydrogen-rich bio-gas but also enhanced the immobilization efficiency of heavy metals. Compared to non-catalytic, when the addition amount of NaOH was 1 wt%, the Zn、Mn、Cd、Pb、Cr accumulated in biochar increased significantly for 76.8, 42.5, 80.8, 75.6 and 80.0%, respectively. This study highlights the remarkable ability of SCWG with alkali catalyst for hydrogen production and heavy metal stabilization. • NaOH promoted real biomass convert into high purity H 2 with carbon captured in-situ. • Carbon fixed in inorganic carbonates benefit carbon-negativity. • Alkali metal catalysts helped heavy metals stabilization. • Main pathways of heavy metals immobilization and transformation investigated. [ABSTRACT FROM AUTHOR]