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Flower-like BiOI was decorated by CdS nanodots and followed by the introduction of iodine vacancies (V I) for photocatalytic sodium lignosulfonate (SLS) valorization under visible light. The iodine vacancies could adjust the band configuration, strengthen the light absorption and act as electron traps, while the intimate contact between BiOI and CdS nanodots provides a high-speed channel for charge transfer. As a consequence, the photocatalytic performance of SLS conversion into value-added vanillin was greatly improved over CdS/BiOI-V I compared with those of CdS, BiOI and CdS/BiOI. The highest yield of vanillin is 10.95 mg/g SLS over CdS/BiOI-V I , about 5, 8.7, 1.3 times those of CdS, BiOI, CdS/BiOI, respectively, and exceeding most related photocatalysts reported elsewhere. More significantly, as to the lignin from Masson pine and alkali lignin, the corresponding vanillin yield can reach 7.04 and 6.54 mg/g lignin , respectively, under the same condition, which suggests the great potential and universality for photocatalytic lignin valorization over such CdS/BiOI-V I heterostructure. [ABSTRACT FROM AUTHOR]

Lignin is abundant and contains a large number of aromatic groups. Herein, Cd x Zn 1-x S photocatalyst with tunable band gap energy was successfully synthesized by using 3-mercaptopropionic acid as a structure tuning additive. Cd x Zn 1-x S can depolymerize alkaline lignin to vanillin by the photocatalytic process. Each gram of alkaline lignin can produce 46.5 mg of vanillin. 2-Phenoxy-1-phenylethanol (PP-ol) and other model compounds were used to understand the depolymerizing process of lignin. Fine tuned Cd x Zn 1-x S can effectively cleave the C β -O-4 bond existed in PP-ol under simulated sunlight. The highest conversion of PP-ol was 89.5% with phenol and acetophenone yields of 66.2% and 33.5%, respectively. The mechanism studies confirm that the C α -H in PP-ol and lignin is firstly dehydrogenated to form C α radical intermediates, and then the photogenerated electrons break the adjacent C β -O bond. This research provides a new strategy to prepare valuable chemicals by virtue of renewable biomass and simulated sunlight. [ABSTRACT FROM AUTHOR]

Catalytic conversion of lignin to certain aromatic compounds has been extensively studied but still has great challenges. Photocatalytic depolymerizing lignin is a very promising method to obtain valuable chemicals. Herein, Zn 4 In 2 S 7 (ZIS)-based photocatalyst was successfully synthesized by simply combining ZIS and graphene oxide (GO). Photocatalyst ZIS-100 can efficiently depolymerize organosolv lignin into phenols and ketones. The relative content of valuable compounds in the depolymerized product was increased by 2.5 times as compared that without photocatalyst. The photocatalyst can effectively break C β -O bonds in 2-phenoxy-1-phenylethanol (PP-ol, a model compound) and the conversion of PP-ol is 93.27%. Mechanism studies show that the thiol groups on the surface of ZIS-100 play an important role in the formation of C α radical intermediates. Photocatalytic cleavage of C β -O bond mainly follows a one-step reaction mechanism through a self‑hydrogen transfer process. This study provides a new strategy for selectively breaking C β -O bond in lignin to form valuable chemicals. [ABSTRACT FROM AUTHOR]