Unravelling the mechanistic role of Ti O C bonding bridge at titania/lignocellulosic biomass interface for Cr(VI) photoreduction under visible light

2019 ◽  
Vol 553 ◽  
pp. 409-417 ◽  
Author(s):  
Ridha Djellabi ◽  
Bo Yang ◽  
Ke Xiao ◽  
Yan Gong ◽  
Di Cao ◽  
...  
Catalysts ◽  
2018 ◽  
Vol 8 (3) ◽  
pp. 94 ◽  
Author(s):  
Ian Dominic Flormata Tabañag ◽  
I-Ming Chu ◽  
Yu-Hong Wei ◽  
Shen-Long Tsai

Climate change is directly linked to the rapid depletion of our non-renewable fossil resources and has posed concerns on sustainability. Thus, imploring the need for us to shift from our fossil based economy to a sustainable bioeconomy centered on biomass utilization. The efficient bioconversion of lignocellulosic biomass (an ideal feedstock) to a platform chemical, such as bioethanol, can be achieved via the consolidated bioprocessing technology, termed yeast surface engineering, to produce yeasts that are capable of this feat. This approach has various strategies that involve the display of enzymes on the surface of yeast to degrade the lignocellulosic biomass, then metabolically convert the degraded sugars directly into ethanol, thus elevating the status of yeast from an immobilization material to a whole-cell biocatalyst. The performance of the engineered strains developed from these strategies are presented, visualized, and compared in this article to highlight the role of this technology in moving forward to our quest against climate change. Furthermore, the qualitative assessment synthesized in this work can serve as a reference material on addressing the areas of improvement of the field and on assessing the capability and potential of the different yeast surface display strategies on the efficient degradation, utilization, and ethanol production from lignocellulosic biomass.


Author(s):  
Yanhong Liu ◽  
Rong-Xiu Zhu ◽  
Chengbu Liu ◽  
Dongju Zhang

DFT and TD-DFT calculations were performed to better understand the photosensitizer-free visible-light-mediated Au-catalyzed cross-couplings between aryldiazonium salts and arylboronic acids. The π–π type complex between the aryldiazonium salt and the...


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