Effect of hydrothermal carbonization temperature on pH, dissociation constants, and acidic functional groups on hydrochar from cellulose and wood

2019 ◽  
Vol 137 ◽  
pp. 138-145 ◽  
Author(s):  
Nepu Saha ◽  
Akbar Saba ◽  
M. Toufiq Reza
Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 173
Author(s):  
Velma Beri Kimbi Yaah ◽  
Satu Ojala ◽  
Hamza Khallok ◽  
Tiina Laitinen ◽  
Marcin Selent ◽  
...  

This paper presents results related to the development of a carbon composite intended for water purification. The aim was to develop an adsorbent that could be regenerated using light leading to complete degradation of pollutants and avoiding the secondary pollution caused by regeneration. The composites were prepared by hydrothermal carbonization of palm kernel shells, TiO2, and W followed by activation at 400 °C under N2 flow. To evaluate the regeneration using light, photocatalytic experiments were carried out under UV-A, UV-B, and visible lights. The materials were thoroughly characterized, and their performance was evaluated for diclofenac removal. A maximum of 74% removal was observed with the composite containing TiO2, carbon, and W (HCP25W) under UV-B irradiation and non-adjusted pH (~5). Almost similar results were observed for the material that did not contain tungsten. The best results using visible light were achieved with HCP25W providing 24% removal of diclofenac, demonstrating the effect of W in the composite. Both the composites had significant amounts of oxygen-containing functional groups. The specific surface area of HCP25W was about 3 m2g−1, while for HCP25, it was 160 m2g−1. Increasing the specific surface area using a higher activation temperature (600 °C) adversely affected diclofenac removal due to the loss of the surface functional groups. Regeneration of the composite under UV-B light led to a complete recovery of the adsorption capacity. These results show that TiO2- and W-containing carbon composites are interesting materials for water treatment and they could be regenerated using photocatalysis.


2013 ◽  
Vol 726-731 ◽  
pp. 634-637 ◽  
Author(s):  
Yan Qiu Lei ◽  
Hai Quan Su

A green and sustainable route for preparation of hydrochars from cornstalk by hydrothermal carbonization (200°C) was described. The morphology of the hydrochars changed with reaction time increased, the surface of the materials contained a large number of functional groups, showed higher adsorption capacity for Cr (VI) than activated carbon and the removal rates of Cr (VI) were 67% and 29% respectively (pH=1, 20°C).


2015 ◽  
Vol 91 ◽  
pp. 574-582 ◽  
Author(s):  
Yousheng Lin ◽  
Xiaoqian Ma ◽  
Xiaowei Peng ◽  
Shanchao Hu ◽  
Zhaosheng Yu ◽  
...  

Carbon ◽  
2013 ◽  
Vol 62 ◽  
pp. 346-355 ◽  
Author(s):  
C. Falco ◽  
J.P. Marco-Lozar ◽  
D. Salinas-Torres ◽  
E. Morallón ◽  
D. Cazorla-Amorós ◽  
...  

2017 ◽  
Vol 7 (1) ◽  
pp. 102-110 ◽  
Author(s):  
Thammarat Koottatep ◽  
Krailak Fakkaew ◽  
Nutnicha Tajai ◽  
Chongrak Polprasert

Low cost adsorbents have been extensively reported for use as a promising substitution for commercial adsorbents for pollutant removal in water and wastewater treatment. In this study, hydrochar produced from the hydrothermal carbonization (HTC) of faecal sludge (FS) (called HTC-hydrochar) was further chemically modified with KOH (called KOH-hydrochar) to improve its surface functional groups, which were suitable for copper (Cu) removal. The adsorption of Cu was conducted using the produced HTC-hydrochar and KOH-hydrochar as absorbents. Experimental results showed the KOH-hydrochar could adsorb Cu at the maximum adsorption capacity of 18.6 mg-Cu/g-hydrochar with Cu removal efficiency of 93%, relatively higher than the HTC-hydrochar and a commercial powdered activated carbon. The quantity of the surface functional groups of the adsorbents was more effective in Cu removal than the surface area. The Cu adsorption mechanism was found to follow the pseudo-second order and intra-particle diffusion models and fit well with Freundlich and Langmuir isotherms. Application of hydrothermal carbonization could be a novel candidate to convert FS into hydrochar which is pathogen free, and to employ the produced hydrochar as an adsorbent to remove Cu from industrial wastewaters.


ACS Omega ◽  
2021 ◽  
Vol 6 (39) ◽  
pp. 25772-25781
Author(s):  
Han Dang ◽  
Guangwei Wang ◽  
Chunmei Yu ◽  
Xiaojun Ning ◽  
Jianliang Zhang ◽  
...  

2021 ◽  
Author(s):  
Shuai Guo ◽  
DanDan Xu ◽  
Xin Guo ◽  
Xingcan Li ◽  
Chenchen Zhao

Abstract The harmful effects of improper sewage sludge (SS) treatment on the environment inspire the search for more benign sludge processing techniques such as hydrothermal carbonization (HTC); the abundant organic matter in SS is used for energy recovery. Herein, response surface methodology (RSM) was used to optimize the HTC-based preparation of SS hydrochar and its gasification performance. Specifically, the hydrochar yield, higher heating value (HHV), and gasification activity index were selected as optimization goals, while carbonization temperature (160–260°C), residence time (30–150 min), and acetic acid concentration (0–1.5 M) were selected as factors influencing the HTC process and CO2-assisted gasification performance. Carbonization temperature was the dominant parameter determining hydrochar yield, HHV, and gasification activity. The hydrochar yield (82.69%) and calorific value (7820.99 kJ kg−1) were maximized under comparatively mild conditions (160°C, 30 min, and 0.07 M acetic acid), whereas the gasification activity index (0.288 s−1) was maximized under harsher conditions (211.34°C, 88.16 min, and 1.58 M acetic acid). The obtained results help to guide the HTC of SS intended for gasification, thus promoting the development of this promising waste-to-energy technology, and may facilitate the design and further optimization of thermochemical SS conversion.


Author(s):  
Martina Klučáková

Abstract Background Humic substances can be considered as polyelectrolytes with supramolecular character and complicated behaviour in water environment. The fractions of humic substances dissolved in water are the most active ones and determinative for their functioning in nature, where the proton-binding and dissociation ability play a crucial role. The dissociation behaviour of humic and fulvic acids can be affected by different circumstances including their concentration which is directly connected with the molecular organization of humic particles in solution and the accessibility of their ionizable functional groups. This study is focused just on these active fractions and their dissociation behaviour in the dependence on their content in studied system. Results Standards and reference samples of International Humic Substances Society were used. Flow-through coulometry was used to determine the total content of acidic functional groups in fulvic solutions and humic leachates. The amount of dissociated acidic groups was determined on the basis of potentiometry. Several differences between the behaviour of humic and fulvic acids were found. While whole samples of fulvic acids including the weakest functional groups were analysed, only the active dissolved humic fractions containing stronger acidic functional groups were characterized. The fractions containing higher amounts of the weakest functional groups remained insoluble. The dissociation degree of fulvic acids decreased with their increasing content, but a maximum on its concentration dependence obtained for humic acids was observed. Conclusions Two different values of dissociation constants were determined for each sample. The first was determined on the basis of the extrapolation of infinite dilution, second was determined as their average value in the region of high concentrations in which it was constant. Obtained values characterize the functioning of dissolved humic substances from point of view of their dissociation ability. The results obtained by this approach can help to predict the acid–base behaviour of dissolved organic carbon in soil and generally in nature. The acid–base behaviour of dissolved organic carbon depends on its ratio to water. It behaves differently in soil which is dry and in soil which is wet or saturated by water.


2021 ◽  
Vol 143 (10) ◽  
Author(s):  
Liwei Wang ◽  
Lin Lu ◽  
Minghua Li ◽  
Yulin Liu ◽  
Xiaohan Ren ◽  
...  

Abstract Activated coke was prepared by mixing sewage sludge and waste poplar bark biomass from furniture manufacturing. The physical activation method of these feedstocks with steam for 1 h at 850 °C was implemented. The elemental composition, pore distribution, microstructure, and surface functional groups of the activated coke products were analyzed by proximate analysis, ultimate analysis, N2 adsorption, scanning electron microscopy, and Fourier transform infrared spectroscopy, respectively. The effects of different mixing ratios of sludge and biomass, preactivation carbonization temperature, and activation method on the activated coke were investigated. When the proportion of biomass was two-thirds of the total feedstock mass and the carbonization temperature was 300 °C, the produced activated coke had the highest specific surface area and the most extended micropore structure. Water vapor (steam) activation was found to be beneficial to the formation of oxygen-containing functional groups. This study established that steam is beneficial to pore expansion and promotes pore development. It was found that the carbonaceous feedstocks acquired initial porosity through carbonization in nitrogen, which proved to be instrumental in the ensuing activation process. After sequential carbonization and activation, the produced active coke acquired a higher specific surface area and microporosity, compared with the active coke produced by activation alone.


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