Volatile organic compounds (VOCs) in cooking oil fumes need to be efficiently removed due to the significant damage they cause to the environment and human health. This review discusses the emission characteristics, which are influenced by different cooking temperatures, cooking oils, and cuisines. Then, various cooking oil fume purification methods are mainly classified into physical capture, chemical decomposition, and combination methods. VOCs removal rate, system operability, secondary pollution, application area, and cost are compared. The catalytic combustion method was found to have the advantages of high VOC removal efficiency, environmental protection, and low cost. Therefore, the last part of this review focuses on the research progress of the catalytic combustion method and summarizes its mechanisms and catalysts. The Marse-van Krevelen (MVK), Langmuir-Hinshelwood (L-H), and Eley-Rideal (E-R) mechanisms are analyzed. Noble metal and non-noble metal catalysts are commonly used. The former showed excellent activity at low temperatures due to its strong adsorption and electron transfer abilities, but the high price limits its application. The transition metals primarily comprise the latter, including single metal and composite metal catalysts. Compared to single metal catalysts, the interaction between metals in composite metal catalysts can further enhance the catalytic performance.

The chemical structures of pyrolytic chars prepared from 32 kinds of Chinese coals were investigated with micro-Raman spectroscopy in this study. Both first-order and second-order Raman spectra of the chars were curve-fitted and analyzed. The effects of the parent coal properties, including coal rank, volatile, fixed carbon, and ash content, on the pyrolytic char structures were detailed discussed and the correlations between these coal properties and pyrolytic char chemical structures were set up. Multiple-factor analysis was done to propose a comprehensive coal property index that relates well to the pyrolytic char chemical structure. The results indicate that the aromatization degree is the key distinguishable structure of pyrolytic chars prepared from coals with various rank, and the alkyl C−H and aryl C−H structures have no significant difference. The aromatization degree of pyrolytic char decreases with the increase of coal rank, while it increases with the increase of the fixed carbon content in parent coals. The high content of moisture in parent coal can induce condensation of the pyrolytic char, but the inorganic composition probably prevents the condensation of the char. Limited correlations between the coal rank, fixed carbon, moisture and ash content, and the aromatization degree of pyrolytic chars were found. A comprehensive coal property index: (fixed carbon content + moisture content)/(volatile content + ash content) (in air dry basis) combining the coal properties together relates well to the aromatization degree of pyrolytic char and can act as a good indicator for the pyrolytic char chemical structure. This study reveals the effects of the parent coal properties, including coal rank, fixed carbon, moisture, and ash content, on the pyrolytic char chemical structure, and provides a new comprehensive coal property index to predict the pyrolytic char chemical structure.

Waste tire (WT) can be heat-treated to be high-quality sulfur self-doped char via pyrolysis and K₂FeO₄-assisted activation processes. This work aimed at further studying the activation mechanisms based on the char structures evolution by operando experimental method. Activation treatment process (from 50 °C to 800 °C and then held for 3 h) was divided into six typical stages (S1–S6) and consisted of carbonization process (S1–S4) and effective activation process (S4–S6). During the carbonization process, the specific capacitance only increased from 0.2 F/g to 12.4 F/g, aromatic ring systems and alkyl-aryl C-C bonds generated, S 2p_3/2 (sulphide bridge) was mainly gradually consumed. During the effective activation process, the specific capacitance hugely increased from 12.4 F/g to 112.5 F/g, aromatic ring systems and alkyl-aryl C-C bonds turned to ordered graphitic char. The pores massively generated from S4 to S5, while micropores partly formed to larger and mesopores+macropores fractionally converting to smaller from S5 to S6. Besides, both S 2p_3/2 and S 2p_5/2 (sulphone bridge) were enriched after S5. Furthermore, the key structural parameters for huge improvement of specific capacitance were found and it further revealed that mesopores+macropores possessed stronger promotion effect than micropores and S 2p_3/2 was more beneficial than S 2p_5/2.