Search

It is still a challenge to find an effective solvent system that can simultaneously dissolve the cellulose and lignin in biomass residues to fabricate lignocellulose hydrogels (LHs). Herein, corncob residues from furfural production were pretreated with alkaline peroxide to regulate the lignin content. The lignin/cellulose composites with various lignin content were then dissolved and regenerated by a green and facile ZnCl

Lignin is abundant and contains a large number of aromatic groups. Herein, CdxZn1-xS photocatalyst with tunable band gap energy was successfully synthesized by using 3-mercaptopropionic acid as a structure tuning additive. CdxZn1-xS 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 CdxZn1-xS can effectively cleave the Cβ-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 Cα-H in PP-ol and lignin is firstly dehydrogenated to form Cα radical intermediates, and then the photogenerated electrons break the adjacent Cβ-O bond. This research provides a new strategy to prepare valuable chemicals by virtue of renewable biomass and simulated sunlight.

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, Zn4In2S7 (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 Cβ-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 Cα radical intermediates. Photocatalytic cleavage of Cβ-O bond mainly follows a one-step reaction mechanism through a self‑hydrogen transfer process. This study provides a new strategy for selectively breaking Cβ-O bond in lignin to form valuable chemicals.

This work investigates the ultraviolet (UV) shielding property of composite films synthesized with graphene oxide (GO) nanosheets and regenerated cellulose. Regenerated cellulose was prepared from ZnCl2/CaCl2/GO solution. The GO sheets presented a homogenous dispersion in the film matrix. The incorporation of GO endows the cellulose films with improved UV shielding capacity. When GO loading reaches 2%, the UVA and UVB blocking percentages are 66.7% and 54.2%, respectively. Moreover, the composite films had excellent visible light transmittance. The resulting films possess promising applications as protective and packing materials.

Bacterial cellulose aerogels were chosen as the substrate for supporting and dispersing metal nanoparticles (Cu and Ni). During the catalyst preparation, we found that the swelling-induced adsorption process could control the metal size and dispersion simultaneously. Cu and Ni nanoparticles were confined into the bacterial cellulose network and SEM results demonstrated that Cu particles had a smaller size compared to Ni particles. The metal-loaded catalysts exhibited good catalytic performance in the 4-nitrophenol reduction reaction. The optimal sample (BC-Cu-0.5) prepared with 0.5 wt% CuSO4 solution could complete the reduction process within 8 min. Besides, the BC-Cu-0.5 catalyst showed excellent stability and reusability. This study sheds light on the deposition of metal particles and provides a wider application for bacterial cellulose.

Trans-arterial chemoembolization (TACE) has been a mainstream treatment for hepatocellular carcinoma (HCC), accordingly there are more requirements for embolic agents’ properties, mainly concentrated on biodegradability and imaging function. A new kind of biodegradable multifunctional porous microspheres (BMPMs) with internal coarse plications are ingeniously designed and manufactured, consisting of carrageenan, inhexol and superparamagnetic iron oxide nanoparticle (SPIO). BMPMs’ sound roundness and excellent swelling behavior guarantee them to be smoothly transported into appointed arteries’ ends and achieve satisfactory embolization effect. Porous structure together with sulphate groups on BMPMs’ skeleton weaved by cross-linked carrageenan contributes to a marvelous doxorubicin hydrochloride (Dox) loading capacity over 45 mg Dox per mL of swollen microspheres, as well as a controllable degradation rate by allowing enzymes to infiltrate into BMPMs through holes, degrading 20–35% after two months in vitro. Inner coarse plications enable BMPMs to effectively combine with iohexol via hydrophilic effect and SPIO by blocking, which can further exhibit a decent imaging performance under digital subtraction system (DSA) and magnetic resonance imaging (MRI) for optimization of current TACE and development of a more advanced imageable TACE (iTACE). Safety evaluation and animal experiment manifest that BMPMs are reliable enough and hold great potential and competitiveness of being used in curing HCC.