This content will become publicly available on July 1, 2024
- Award ID(s):
- 2123495
- NSF-PAR ID:
- 10475656
- Publisher / Repository:
- MDPI
- Date Published:
- Journal Name:
- Energies
- Volume:
- 16
- Issue:
- 14
- ISSN:
- 1996-1073
- Page Range / eLocation ID:
- 5534
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
Hydrothermal carbonization (HTC) is a prominent thermochemical technology that can convert high-moisture waste into a valuable product (called hydrochar) at a relatively mild treatment condition (180–260 °C and 2–10 MPa). With rapidly growing research on HTC and hydrochar in recent years, review articles addressing the current and future direction of this research are scarce. Hence, this article aims to review various emerging applications of hydrochars, e.g., from solid fuel to soil amendment, from electron storage to hydrogen storage, from dye adsorption, toxin adsorption, heavy metal adsorption to nutrient recovery, and from carbon capture to carbon sequestration, etc. This article further provides an insight in the hydrochar’s working mechanism for various applications and how the applications can be improved through chemical modification of the hydrochar. Finally, new perspectives with appropriate recommendations have been made to further unveil potential applications and its improvement through hydrochar and its modified version.more » « less
-
Rauch, W Liu (Ed.)Water contamination by nitrogen and phosphorus ions has a direct consequence of eutrophication to the ecosystem. The objective of this study is to investigate the production of hydrochars by acetic acid or sodium hydroxide assisted hydrothermal carbonization (HTC), various activation methods, and the potential of hydrochar as an adsorbent to remove NH4+-N and PO43--P from wastewater. The results showed that acetic acid or sodium hydroxide assisted HTC and activation with magnesium chloride or air could improve the surface properties of hydrochar. Acetic acid modification generated extensive oxygenated functional groups, while sodium hydroxide modification produced hydrochar with a high N/C ratio and surface aromaticity. Treating hydrochar with magnesium chloride could impregnate nano-magnesium particles on the hydrochar, thereby improving the ability to remove N and P. Air activation of hydrochar resulted in more oxygen containing functional groups. The NH4+-N and PO43--P adsorption capacities of these hydrochars ranged from 92.6 to 122.4mg/g and 1.6 to 15.8mg/g, respectively. The adsorption capacity of hydrochars in swine wastewater is similar to the results of artificial wastewater. The results suggested that Mg-nanoparticle dispersion and oxygen-containing functional groups played a major role in adsorption than ion exchange and physisorption.more » « less
-
Rauch, Wolfgang ; null (Ed.)Water contamination by nitrogen and phosphorus ions has a direct consequence of eutrophication to the ecosystem. The objective of this study is to investigate the production of hydrochars by acetic acid or sodium hydroxide assisted hydrothermal carbonization (HTC), various activation methods, and the potential of hydrochar as an adsorbent to remove NH4+-N and PO43−-P from wastewater. The results showed that acetic acid or sodium hydroxide assisted HTC and activation with magnesium chloride or air could improve the surface properties of hydrochar. Acetic acid modification generated extensive oxygenated functional groups, while sodium hydroxide modification produced hydrochar with a high N/C ratio and surface aromaticity. Treating hydrochar with magnesium chloride could impregnate nano-magnesium particles on the hydrochar, thereby improving the ability to remove N and P. Air activation of hydrochar resulted in more oxygen containing functional groups. The NH4+-N and PO43−-P adsorption capacities of these hydrochars ranged from 92.6 to 122.4mg/g and 1.6 to 15.8mg/g, respectively. The adsorption capacity of hydrochars in swine wastewater is similar to the results of artificial wastewater. The results suggested that Mg-nanoparticle dispersion and oxygen-containing functional groups played a major role in adsorption than ion exchange and physisorption.more » « less
-
Abstract Producing hydrochar from landfill municipal solid wastes (MSW) is a sustainable alternative to existing waste management practices in low‐ and middle‐income countries. In this study, mixed MSW feedstock (sent for landfilling) was subjected to hydrothermal carbonization to produce hydrochars. The hydrochar showing the highest heating value was subjected to pyrolysis at 5, 10, and 20 K min−1heating rates. Based on the pyrolysis characteristics, a three pseudo‐component‐based distributed activation energy model was employed to describe the pyrolysis kinetics. The activation energy distributions for the three pseudo‐components were 140 ± 8.7 kJ mol−1, 190 ± 1 kJ mol−1and 175.9 ± 24.9 kJ mol−1, which were able to predict the pyrolysis profile at all heating rates with
R 2 > 0.999. Differential thermogravimetric profiles of the hydrochar revealed its pyrolytic reactivity to resemble lignocellulosic constituents. Fourier‐transform infrared analysis of the hydrochar showed retention of oxygen‐containing functional groups (associated with lignocellulosic constituents) from the parent feedstock. © 2022 Society of Chemical Industry and John Wiley & Sons, Ltd. -
Biofuels produced via thermochemical conversions of waste biomass could be sustainable alternatives to fossil fuels but currently require costly downstream upgrading to be used in existing infrastructure. In this work, we explore how a low-cost, abundant clay mineral, bentonite, could serve as an in situ heterogeneous catalyst for two different thermochemical conversion processes: pyrolysis and hydrothermal carbonization (HTC). Avocado pits were combined with 20 wt% bentonite clay and were pyrolyzed at 600 °C and hydrothermally carbonized at 250 °C, commonly used conditions across the literature. During pyrolysis, bentonite clay promoted Diels–Alder reactions that transformed furans to aromatic compounds, which decreased the bio-oil oxygen content and produced a fuel closer to being suitable for existing infrastructure. The HTC bio-oil without the clay catalyst contained 100% furans, mainly 5-methylfurfural, but in the presence of the clay, approximately 25% of the bio-oil was transformed to 2-methyl-2-cyclopentenone, thereby adding two hydrogen atoms and removing one oxygen. The use of clay in both processes decreased the relative oxygen content of the bio-oils. Proximate analysis of the resulting chars showed an increase in fixed carbon (FC) and a decrease in volatile matter (VM) with clay inclusion. By containing more FC, the HTC-derived char may be more stable than pyrolysis-derived char for environmental applications. The addition of bentonite clay to both processes did not produce significantly different bio-oil yields, such that by adding a clay catalyst, a more valuable bio-oil was produced without reducing the amount of bio-oil recovered.more » « less