The effects of ultrasonic and ozonation pretreatments on organic solubilization, anaerobic biodegradability, and biogas production were elucidated in this study. Two pretreatment methods for batch anaerobic digestion for biogas recovery with the same material and experimental conditions were the focus for comparison. Anaerobic digestion experiments were conducted at ambient temperature with the solid retention time set to 25 days. The obtained results indicated that the soluble chemical oxygen demand increased from 0.344 without pretreatment to 1.023 and 1.228 g/L with ultrasound and ozone pretreatments, respectively, whereas the yields of biogas production in the 25 days increased by 32.3 and 52.9% via ultrasonic irradiation and ozonation relative to the control case, respectively. The biodegradability of the organic compounds of the samples for the cases of ultrasound, ozone pretreatments, and control achieved 55.9, 64.31, and 39.18%, respectively, in terms of chemical oxygen demand (COD) removal efficiencies. The physicochemical characteristics of sludge flocs were investigated via scanning with particle sizes, which were obviously affected by pretreatments of sonication and ozonation, resulting in finer particles than in the control case.
Combined heat and power production from biogas is now playing an important role in energy and resource utilization as well as pollution control in waste water treatment. This research used biogas from the Bali Sewage Treatment Plant in New Taipei City, Taiwan, as a major source of fuel for the electricity generation. A micro gas turbine electricity generator, Capstone CR-30, which possesses a maximum rated power load (PWL) of 30 kW, was equipped to convert biogas into electricity. The biogas is mainly composed of CH4 (56.1 ± 8.0 vol.%), CO2 (25.5 ± 9.8 vol.%), H2 (0.5 vol.%), and H2S (0.99 ± 0.07 ppmv). During the test operation period of the generator, it was found that the thermal efficiency increases from 19.8% to 23.4% kWhe/kWhth, while the electricity generation efficiency (ηEB) also rises from 0.93 to 1.09 kWhe/m3 biogas as the PWL increases from 10 kW to 30 kW. The results indicated that the generator has a better performance with higher PWL. At PWL = 30 kW, the average adjusted concentrations of CO and NOx (adjusted to 15 vol.% O2) emitted from the generator are 86 ppmv and 17 ppmv, respectively. Both are much lower than the emission standards of stationary sources in Taiwan of 2000 ppmv and 150 ppmv, respectively. Thus, PWL of 30 kW was selected in cooperation with biogas inflow = 0.412 m3/min and air/fuel ratio (i.e., air/biogas ratio) = 76.0 vol./vol. for the long-term regular operation. At the above setting conditions for long-term operation, the generator continuously consumed the biogas and provided stable electricity generation at a rate of 19.64 kWhe/h for a 2-year running period. Moreover, the greenhouse gas can be cut off with a rate of 10.78 kg CO2e/h when using biogas as fuel for electricity generation. Overall, this research proves that the application of a micro gas turbine electricity generator not only has promising performance for using biogas but also gives a significant reduction of greenhouse gas emission, which fits the concepts of the circular economy and environmental protection.
This study explores the possibility of applying high-gravity rotating packed bed (HGRPB) in removing H2S and CO2 from biogas. Ca(OH)2 aqueous solution was used as the absorbent in this study. Different experimental conditions including solution pH, rotating speed (R S) of HGRPB, gas flow rate (Q G), and liquid flow rate (Q L) were investigated with respect to the removal efficiency (E) of H2S and CO2. The experimental and simulated results show that the optimal removal efficiency of H2S and CO2 using HGRPB achieved nearly the same as 99.38 and 99.56% for removal efficiency of H2S and 77.28 and 77.86% for removal efficiency of CO2, respectively. Such efficiencies corresponded with the following optimal conditions: a solution pH of 12.26, HGRPB reactor with the rotating speed of 1,200 rpm, the gas flow rate of 2.46 (L/min), and the liquid flow rate of 0.134 (L/min).
A method for producing ferulic acid by ultrasound-assisted, homogeneous, base-catalyzed hydrolysis of γ-oryzanol was developed. Experiments were conducted using various reaction temperatures and ratios of γ-oryzanol to base catalyst in both homogeneous and heterogeneous systems. The reaction performed without ultrasound under the homogeneous conditions of potassium hydroxide/γ-oryzanol ratio (wt/wt) 20 : 1 and 75°C gave a ferulic acid yield of 83.3% in 3 h. Acceleration of the homogeneous reaction using ultrasound irradiation at 20 (horn type) and 200 kHz (planar type) was explored by evaluating the kinetic parameters. At 30°C, the ratios of ultrasonic irradiation at low (20 kHz, 50 W) and high (200 kHz, 50 W) frequencies versus those of the heating method increased by 2.0- and 1.4-fold in comparison with those at 60°C, respectively. The contribution of ultrasonic irradiation (50 W) to the hydrolysis reaction decreased with increase of temperature. However, irradiation at 20 kHz and a power of 180 W gave a 94% ferulic acid yield at 60°C in 3 h. These results indicate that the use of low frequency (horn type and high-power irradiation) enabled yields higher than 90% to be obtained.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.