Publications by authors named "Ya-Ya Ma"

Sequential extract residues (R , = 1, 2, 3, 4, and 5) were obtained from Hefeng acid-washing coal (HF) by petroleum ether, carbon disulfide, methanol, acetone, and isometric carbon disulfide/acetone mixture, sequentially. Pyrolysis behavior of the residues was determined using thermogravimetry analysis. The Coats-Redfern method with different reaction orders was used to analyze the pyrolysis kinetic of each sample, and the kinetic parameters, including correlation coefficient ( ), activation energy (), and pre-exponential factor (), were calculated.

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Taking five coal samples (FCSs) in Xinjiang as the research object, characterizations such as proximate analysis, ultimate analysis, Fourier transform infrared (FTIR), and thermogravimetry-differential thermal analysis (TG-DTG) were carried out. The Coats-Redfern model was used to simulate pyrolysis kinetics of FCSs under different reaction orders (ROs). The results showed that except for HSBC, the of the other four coal samples are all higher than 0.

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Article Synopsis
  • Different solvents (NMP, Py, THF, THN) were used to swell Hefeng acid-washed bituminous coal (HBC), with NMP showing the best swelling performance (a swelling degree of 2.11).
  • The FTIR analysis indicated that both the acid washing and swelling processes had minimal impact on the coal's macromolecule structure, meaning the coal remained intact.
  • Methanol extraction yields were higher after acid washing, achieving 3.21% for swelled HBC compared to 1.66% for unwashed HBC, suggesting that acid washing improved the extraction efficiency.
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The direct regio- and enantioselective C6 functionalization of 2,3-disubstituted indoles with azadienes has been developed using chiral phosphoric acid as catalyst, providing a convenient approach to synthesize the optically active heterotriarylmethanes with excellent yields, broad substrate scope, and up to 98% ee. Mechanistic studies revealed that -alkylation of 2,3-disubstituted indoles with azadienes would be reversible, and enantioselective C6 functionalization could be enabled.

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