CO2 Reduction to Valuable Chemicals on TiO2-Carbon Photocatalysts Deposited on Silica Cloth

A new photocatalyst for CO2 reduction has been presented. The photocatalyst was prepared from a combination of a commercial P25 with a mesopore structure and carbon spheres with a microporous structure with high CO2 adsorption capacity. Then, the obtained hybrid TiO2-carbon sphere photocatalysts were deposited on a glass fiber fabric. The combined TiO2-carbon spheres/silica cloth photocatalysts showed higher efficiency in the two-electron CO2 reduction towards CO than in the eight-electron reaction to methane. The 0.5 g graphitic carbon spheres combined with 1 g of TiO2 P25 resulted in almost 100% selectivity to CO. From a practical point of view, this is promising as it economically eliminates the need to separate CO from the gas mixture after the reaction, which also contains CH4 and H2.

Cell Wall Pore Structures of Bamboo as Relation to Species and Tissue Types

Efficient convention of bamboo biomass into biofuel and biomaterials, as well as chemical treatment are both highly related to the porosity of cell wall. The present work characterizes the micropore and mesopore structure in cell walls of six different bamboo species and tissue types using CO2 and N2 adsorption. Two plantation wood species were also tested for comparison. Bamboo species normally showed lower cell wall porosity (2.64%-3.75%) than wood species (3.98%-5.06%), indicating a more compact structure for bamboo than wood. A distinct species dependence of cell wall pore structures and porosity was also observed. Furthermore, the cell wall pore structure and porosity are shown to be tissue-specific, as the parenchyma cells exhibit higher pore volume and porosity compared to bamboo fibers. The obtained results give new explanations on the known facts that both bamboo and bamboo fibers exhibit higher biomass recalcitrance as compared to wood and bamboo parenchyma cells, constructing the base of pretreatment optimization and subsequent processing for bamboo-derived biofuels and biomaterials.

Product Characteristics of Sludge Pyrolysis and Adsorption Performance of Metals by Char

The microwave heating system was used for sludge pyrolysis. The raw sludge and KOH-immersed sludge were pyrolyzed and their product characteristics were determined. The research results are advantageous to understand the influence of KOH activation on characteristics of pyrolysis products and the adsorption performance of metals in char. In the case of a high temperature and high KOH dose, most of the lost mass from sludge pyrolysis was converted into gaseous products instead of oil. The heat values of liquid oils were 40.86–41.39 MJ kg−1, which has the potential for use as fuels. The use of a higher KOH dose for sludge pyrolysis is beneficial to the porosity development and generates a mesopore structure. The results from adsorption tests indicate that precipitation could be the dominant adsorption mechanism due to the binding between alkaline anion and carbonate and metal ions with a strong chemical affinity. The high KOH dose sludge adsorbent has a remarkable adsorption performance and can be used as adsorbent for the removal of the studied metals.

Influence of Evaporation Drying on the Porous Properties of Carbon/Carbon Composite Xerogels

Carbon/carbon (C/C) composite xerogels dried by evaporation were prepared in this study to observe the change of their porous properties and their morphology by nitrogen sorption apparatus and a scanning electron microscope. Resorcinol and formaldehyde (RF) sols as a matrix phase and cotton fibers (CF) as a dispersed phase were mixed and gelated to be CF/RF composite hydrogels. The composite hydrogels were exchanged by t-butanol (TBA), dried by evaporation at 50 °C, and carbonized at 1000 °C to become the C/C composite xerogels. The results show that the CF addition does not decrease the mesoporous properties of the C/C composite xerogels. Moreover, the CF addition can alleviate the pore shrinkage, and it can maintain the mesopore structure. The mesopore size and the micropore size of C/C composites are insignificantly changed because the CF addition and the solvent exchange using TBA may suppress the pore shrinkage despite the gas-liquid interface existing during the evaporation drying.

Carbon Black as Conductive Additive and Structural Director of Porous Carbon Gels

This work investigates the impact of carbon black (CB) as a porogenic agent and conductive additive in the preparation of electrically conductive nanoporous carbon gels. For this, a series of materials were prepared by the polycondensation of resorcinol/formaldehyde mixtures in the presence of increasing amounts of carbon black. The conductivity of the carbon gel/CB composites increased considerably with the amount of CB, indicating a good dispersion of the additive within the carbon matrix. A percolation threshold of ca. 8 wt.% of conductive additive was found to achieve an adequate “point to point” conductive network. This value is higher than that reported for other additives, owing to the synthetic route chosen, as the additive was incorporated in the reactant’s mixture (pre-synthesis) rather than in the formulation of the electrodes ink (post-synthesis). The CB strongly influenced the development of the porous architecture of the gels that exhibited a multimodal mesopore structure comprised of two distinct pore networks. The microporosity and the primary mesopore structure remained rather unchanged. On the contrary, a secondary network of mesopores was formed in the presence of the additive. Furthermore, the average mesopore size and the volume of the secondary network increased with the amount of CB.

Sustainable lignin-derived hierarchically porous carbon for capacitive deionization applications

Cross-linked lignin with glyoxal leads to a support mesopore structure of lignin-based porous carbon with improved capacitive deionization performance.