Characterizing Adsorption Performance of Granular Activated Carbon with Permittivity.
Ontology highlight
ABSTRACT:
SUBMITTER: Yang Y
PROVIDER: S-EPMC5503362 | biostudies-other | 2017 Mar
REPOSITORIES: biostudies-other
Similar Datasets
Project description:Nitrification and distillation of urine allow for the recovery of all nutrients in a highly concentrated fertilizer solution. However, pharmaceuticals excreted with urine are only partially removed during these two process steps. For a sustainable and safe application, more extensive removal of pharmaceuticals is necessary. To enhance the pharmaceutical removal, which is already occurring during urine storage, nitrification and distillation, an adsorption column with granular activated carbon (GAC) can be included in the treatment train. We executed a pilot-scale study to investigate the adsorption of eleven indicator pharmaceuticals on GAC. During 74 days, we treated roughly 1000 L of pre-filtered and nitrified urine spiked with pharmaceuticals in two flow-through GAC columns filled with different grain sizes. We compared the performance of these columns by calculating the number of treated bed volumes until breakthrough and carbon usage rates. The eleven spiked pharmaceuticals were candesartan, carbamazepine, clarithromycin, diclofenac, emtricitabine, hydrochlorothiazide, irbesartan, metoprolol, N4-acetylsulfamethoxazole, sulfamethoxazole and trimethoprim. At the shortest empty bed contact time (EBCT) of 25 min, immediate breakthrough was observed in both columns shortly after the start of the experiments. Strong competition by natural organic material (NOM) could have caused the low pharmaceutical removal at the EBCT of 25 min. At EBCTs of 70, 92 and 115 min, more than 660 bed volumes could be treated until breakthrough in the column with fine GAC. The earliest breakthrough was observed for candesartan and clarithromycin. On coarse GAC, only half the number of bed volumes could be treated until breakthrough compared to fine GAC. The probable reason for the later breakthrough with fine GAC is the smaller intraparticle diffusive path length. DOC and UV absorbance measurements at 265 nm indicated that both parameters can be used as indicators for the breakthrough of pharmaceuticals. In contrast to pharmaceuticals and DOC, the nutrient compounds ammonium, nitrate, phosphate, potassium and sulfate were not removed significantly. A comparison with literature values suggests that the amount of GAC needed to remove pharmaceuticals from human excreta could be reduced by nearly two orders of magnitude, if urine were treated on site instead of being discharged and treated in a centralized wastewater treatment plant.
| S-EPMC7298675 | biostudies-literature
Project description:This study measured chlorine- and chloramine-reactive precursors using formation potential (FP) tests of nine U.S. Environmental Protection Agency (EPA) regulated and 57 unregulated disinfection byproducts (DBPs) in tertiary-filtered wastewater before and after pilot-scale granular activated carbon (GAC) adsorption. Using breakthrough of precursor concentration and of concentration associated calculated cytotoxicity and genotoxicity (by correlating known lethal concentrations reported elsewhere), the performance of three parallel GAC treatment trains were compared against tertiary-filtered wastewater: ozone/GAC, chlorine/GAC, and GAC alone. Results show GAC alone was the primary process, versus ozone or chlorine alone, to remove the largest fraction of total chlorine- and chloramine-reactive DBP precursors and calculated cytotoxicity and genotoxicity potencies. GAC with pre-ozonation removed the most chlorine- and chloramine-reactive DBP precursors followed by GAC with pre-chlorination and lastly GAC without pre-treatment. GAC with pre-ozonation produced an effluent with cytotoxicity and genotoxicity of DBPs from FP that generally matched that of GAC without pre-oxidation; meanwhile removal of toxicity was greater by GAC with pre-chlorination. The cytotoxicity and genotoxicity of DBPs from FP tests did not scale with DBP concentration; for example, more than 90% of the calculated cytotoxicity resulted from 20% of the DBPs, principally from haloacetaldehydes, haloacetamides, and haloacetonitriles. The calculated cytotoxicity and genotoxicity from DBPs associated with FP-chloramination were at times higher than with FP-chlorination though the concentration of DBPs was five times higher with FP-chlorination. The removal of DBP precursors using GAC based treatment was at least as effective as removal of DOC (except for halonitromethanes for GAC without pre-oxidation and with pre-chlorination), indicating DOC can be used as an indicator for DBP precursor adsorption efficacy. However, the DOC was not a good surrogate for total cytotoxicity and genotoxicity breakthrough behavior, therefore, unregulated DBPs could have negative health implications that are disconnected from general water quality parameters, such as DOC, and regulated classes of DBPs. Instead, cytotoxicity and genotoxicity correlate with the concentration of specific classes of unregulated DBPs.
| S-EPMC7522497 | biostudies-literature
Project description:Physical adsorption on activated carbons has shown to be a very attractive methodology for CO2 separation from flue gas streams and biogas. In this context, the goal of this work was to prepare granular activated carbons intended for CO2 adsorption from an abundant and low-cost biomass residue (coconut shell) by using practical and cost-effective procedures. By the first time, parameters involved in chemical activation with dehydrating agents (H3PO4 or ZnCl2) and/or physical activation with CO2 were systematically screened in depth in order to obtain materials with improved performance for CO2 adsorption on a volume basis. Compared with the commonly used mass basis, the data expressed on a volume basis are very important for industrial applications because they permit to estimate the efficiency of a fixed bed adsorption column. The work permitted to prepare granular activated carbons with a blend of relatively high gravimetric CO2 uptake and bulk density, so that high volumetric CO2 uptakes were attained. The highest values were 2.67 and 1.17 mmol/cm3 for CO2 pressures of 1.0 and 0.15 bar, respectively. It is remarkable that the obtained results were similar to those reported by other authors for carbons chemically activated with KOH, the activation methodology that has been widely claimed as the one that produce ACs with the best performances for CO2 adsorption, but which involves severe restrictions. Therefore, the present work can be considered a very important step in paving the way toward making CO2 adsorption an each time more interesting technology to reduce the emissions of anthropogenic greenhouse gases.
| S-EPMC7718001 | biostudies-literature
Project description:Straw is one of the largest agricultural biowastes and a potential alternative precursor of activated carbon. Activated carbon prepared from different types of straw have great differences in structure and adsorption performance. In order to explore the performance of different straw-based activated carbon in volatile organic compounds adsorption, five common straws were selected as potential source materials for the preparation of SAC. The straw-based activated carbons were prepared and characterized via a thermo-gravimetric analysis, scanning electron microscope and the Brunauer-Emmett-Teller method. Among the five straw-based activated carbons, millet straw-derived activated carbon exhibited superior properties in SBET, Smic and adsorption capacities of both toluene and ethyl acetate. Furthermore, the preparation process of millet straw activated carbon was optimized via response surface methodology, using carbonization temperature, carbonization time and impregnation ratio as variables and toluene adsorption capacity, ethyl acetate adsorption capacity and activated carbon yield as responses. The optimal preparation conditions include a carbonization temperature of 572 °C, carbonization time of 1.56 h and impregnation ratio (ZnCl2/PM, w/w) of 1.60, which was verified experimentally, resulting in millet straw activated carbon with a toluene adsorption capacity of 321.9 mg/g and ethyl acetate adsorption capacity of 240.4 mg/g. Meanwhile, the adsorption isothermals and regeneration performance of millet straw activated carbon prepared under the optimized conditions were evaluated. The descriptive ability of the isothermals via the Redlich-Peterson equation suggests a heterogeneous surface on millet straw activated carbon. Recyclability testing has shown that millet straw activated carbon maintained a stable adsorption capacity throughout the second to fifth cycles. The results of this work indicate that millet straw activated carbon may be a potential volatile organic compound adsorbent for industrial application.
| S-EPMC8232107 | biostudies-literature
Project description:It is still a great challenge to develop a new porous carbon adsorbent with excellent separation performance and to recover low-concentration CH4 in coal mine gas. This work provides a new idea for the study of CH4 adsorption on activated carbon (AC) composites. Composite materials with microporous structures were prepared from coconut-shell activated carbon (CAC) doped with graphene oxide (GO) by a chemical activation process in this paper. The expansion and dissociation of GO at high temperatures indirectly improve the specific surface area (SSA) of the composite. The interlayer aggregation is reduced, the activation effect is improved, and a new low-cost adsorption material is prepared. The SSA of CAC-50 is more than 3000 m2·g-1. A high SSA and a narrow pore size distribution lead to a higher total adsorption capacity of CH4. The breakthrough test also confirmed that AC/GOs had a better adsorption capacity for CH4. The separation performance of the CH4/N2 mixture is not good at room temperature, which is due to the influence of a high SSA and average pore size. As a low-cost and rich material, CAC has a wide range of application prospects. The composite is a potential material for recovering low-concentration CH4 from the coal mine, which is worthy of attention. In the future, the selectivity of AC/GOs to CH4 can be increased by loading functional groups or modification.
| S-EPMC8340399 | biostudies-literature
Project description:Adsorption and desorption behaviors of tetracycline hydrochloride by activated carbon-based adsorbents derived from sugar cane bagasse modified with ZnCl2 were investigated. The activated carbon was tested by SEM, EDX, BET, XRD, FTIR, and XPS. This activated carbon exhibited a high BET surface area of 831 m2 g-1 with the average pore diameter and pore volume reaching 2.52 nm and 0.45 m3 g-1, respectively. The batch experimental results can be described by Freundlich equation, pseudo-second-order kinetics, and the intraparticle diffusion model, while the maximum adsorption capacity reached 239.6 mg g-1 under 318 K. The effects of flow rate, bed height, initial concentration, and temperature were studied in fixed bed adsorption experiments, and adsorption data were fitted with six dynamic adsorption models. The results of characterizations and the batch experiments were analyzed to study the adsorption and desorption mechanisms. Tetracycline hydrochloride and activated carbon were bonded together by ?-? interactions and cation-? bonds. Ethanol was used as an eluent which bonded with 10 hydrogen bond acceptors on tetracycline hydrochloride to form a complex by hydrogen bonding to achieve recycling.
| S-EPMC6943745 | biostudies-literature
Project description:The present work investigated the application of granular activated carbon (GAC) derived from date palm pits (DPP) agricultural waste for treating gaseous ammonia. Respective findings indicate increased breakthrough time (run time at which 5% of influent ammonia is exiting with the effluent gas) with a decrease in influent ammonia and increase in GAC bed depth. At a gas flow rate of 1.1 L/min and GAC column length of 8 cm, the following breakthrough trend was noted: 1295 min (2.5 ppmv) > 712 min (5 ppmv) > 532 min (7.5 ppmv). A qualitatively similar trend was also noted for the exhaustion time results (run time at which 95% of influent ammonia is exiting with the effluent gas). The Fourier Transform Infrared Spectroscopy (FTIR) findings for the produced GAC indicated some salient functional groups at the produced GAC surface including O-H, C-H, C-O, and S=O groups. Ammonia adsorption was suggested to result from its interaction with the respective surface functional groups via different mechanisms. Comparison with a commercial GAC showed the date palm pits based GAC to be having slightly higher breakthrough and exhaustion capacity.
| S-EPMC7084576 | biostudies-literature
Project description:In view of the characteristics and risks of ammonia, its removal is important for industrial production and environmental safety. In this study, viscose-based activated carbon fiber (ACF) was used as a substrate and chemically modified by nitric acid impregnation to enhance the adsorption capacity of the adsorbent for ammonia. A series of modified ACF-based adsorbents were prepared and characterized using BET, FTIR, XPS, and Boehm titration. Isotherm tests (293.15 K, 303.15 K, 313.15 K) and dynamic adsorption experiments were performed. The characterization results showed that impregnation with low concentrations of nitric acid not only increased the surface acidic functional group content but also increased the specific surface area, while impregnation with high concentrations of nitric acid could be able to decrease the specific surface area. ACF-N-6 significantly increased the surface functional group content without destroying the physical structure of the activated carbon fibers. The experimental results showed that the highest adsorption of ammonia by ACFs was 14.08 mmol-L-1 (ACF-N-6) at 293 K, and the adsorption capacity was increased by 165% compared with that of ACF-raw; by fitting the adsorption isotherm and calculating the equivalent heat of adsorption and thermodynamic parameters using the Langmuir-Freundlich model, the adsorption process could be found to exist simultaneously. Regarding physical adsorption and chemical adsorption, the results of the correlation analysis showed that the ammonia adsorption performance was strongly correlated with the carboxyl group content and positively correlated with the relative humidity (RH) of the inlet gas. This study contributes to the development of an efficient ammonia adsorption system with important applications in industrial production and environmental safety.
| S-EPMC10648919 | biostudies-literature
Project description:The depth profile of mercuric ion after the reaction with polysulfide-rubber-coated activated carbon (PSR-AC) was investigated using micro-X-ray fluorescence (?-XRF) imaging techniques and mathematical modeling. The ?-XRF results revealed that mercury was concentrated at 0-100 ?m from the exterior of the particle after 3 months of treatment with PSR-AC in 10 ppm HgCl(2) aqueous solution. The ?-X-ray absorption near edge spectroscopic (?-XANES) analyses indicated HgS as a major mercury species, and suggested that the intra-particle mercury transport involved a chemical reaction with PSR polymer. An intra-particle mass transfer model was developed based on either a Langmuir sorption isotherm with liquid phase diffusion (Langmuir model) or a kinetic sorption with surface diffusion (kinetic sorption model). The Langmuir model predicted the general trend of mercury diffusion, although at a slower rate than observed from the ?-XRF map. A kinetic sorption model suggested faster mercury transport, which overestimated the movement of mercuric ions through an exchange reaction between the fast and slow reaction sites. Both ?-XRF and mathematical modeling results suggest mercury removal occurs not only at the outer surface of the PSR-AC particle but also at some interior regions due to a large PSR surface area within an AC particle.
| S-EPMC3265622 | biostudies-literature
Project description:Raw materials, activation methods, and post-activation treatment used in manufacturing granular activated carbon (GAC) results in a spectrum of physicochemical characteristics that potentially impact the adsorption oxidation treatment process. A comprehensive study is lacking that assesses the effect of GAC characteristics on adsorption oxidation treatment of contaminant spent-GAC. Consequently, it is inherently assumed the treatment process is GAC-independent. Here, GACs (n = 31) were characterized and used in the hydrogen peroxide (H2O2)-based adsorption oxidation treatment of 2-chlorophenol (2CP)-spent GAC. The GACs exhibited a range in surface area, pore volume distribution, metals content, surface functionality, and H2O2 reaction. Chloride recovery, the treatment metric for 2CP oxidation, indicated a wide range in oxidation (0-49.2%) where bituminous- and wood-based GAC performed best. A selected subset of GACs (n = 12), amended with iron, methyl tert-butyl ether (MTBE), and H2O2, exhibited a range in oxidative treatment (1.1-57.9%). Correlations were established between GAC surface functionality, H2O2 reactivity, adsorption, and MTBE oxidation indicating multiple parameters play a collective and compounding role. The order of GACs successfully used in the treatment process is bituminous-based coal > wood > coconut > peat. Results showed adsorption oxidation treatment is GAC-dependent, and therefore, GAC selection is a key factor in the success of this technology.
| S-EPMC7944943 | biostudies-literature