ABSTRACT
This work introduced a new way of fabricating a granular material with the supply of Al-rich precipitates selectively obtained from acid mine drainage (AMD), and its potential as a promising adsorbent for fluoride (F) was evaluated. Through the selective sequential precipitation (SP) process in the field, Al-rich precipitates with high purity (>81%) were collected at the high recovery rate (>99.8%) as a raw material for adsorbent fabrication. The granular adsorbent (ALB) was synthesized through encapsulation of precipitate powders by chemically inducing polymeric bead formation. The characterization results revealed that ALB possessed a highly porous structure and embedded a large number of nanoparticles of amorphous Al hydroxides inside its framework. Less adsorption of F occurred at an alkaline pH condition due to the competitive effect of hydroxyl ions. The adsorption process can be divided into fast adsorption by the outer surface and slow diffusion in the inner phase. The maximum adsorption capacity of ALB for F was calculated to be 17.7 mg g-1 in the Langmuir isotherm model fitting results. By the repetitive adsorption/desorption and XPS results, it turned out that both chemisorption and physisorption gave a contribution in the removal of F, and the regeneration of adsorbent using NaOH was effective to restore the adsorption capability but accompanied the loss of adsorption sites. As a result, it can be concluded that a granule-type material fabricated using Al-rich precipitates selectively recovered from AMD neutralization can be considered as a promising adsorbent for F removal in aqueous solution.
Subject(s)
Water Pollutants, Chemical , Water Purification , Adsorption , Aluminum , Fluorides , Hydrogen-Ion Concentration , Kinetics , Water Pollutants, Chemical/analysisABSTRACT
This work newly employed monoclinic zirconia (ZrO2) as a promoter to improve CO2 pyrolysis of coffee waste (CW). The CO2 pyrolysis of CW presented the high level of CO production (14.3â¯mol%) during two stages of non-isothermal (280 to 700⯰C) and isothermal pyrolysis (kept at 700⯰C). At the same condition, the incorporation of ZrO2 improved the CO generation up to about twice that of CW (29.5â¯mol%) by possibly inducing more conversion of pyrolytic oil into gas. The characterization results exhibited that ZrO2-impregnated biochar (ZrB) possessed the distinctive surface morphology that highly graphitic- and porous carbon layers were covered by ZrO2 nanoparticle clusters. In a series of adsorption experiments, ZrB composite showed pH-dependent As(V) adsorption and pH neutralization ability. The adsorption proceeded relatively rapid with 95% removal during 120â¯min in the early stage, followed by 5% removal in the remaining 240â¯min. The maximum adsorption capacity was found to be 25.2â¯mgâ¯g-1 at final pH 8. The reusability and stability of ZrB were demonstrated in the 6 consecutive cycles of adsorption/desorption. As a result, ZrO2-assisted CO2 pyrolysis can potentially produce fuel gas with high CO fraction and composite adsorbent suitable for As(V) removal in acidic wastewater.
Subject(s)
Carbon Dioxide/chemistry , Carbon Monoxide/analysis , Charcoal/chemistry , Coffea/chemistry , Pyrolysis , Refuse Disposal/methods , Zirconium/chemistry , Adsorption , Chromium/analysis , Seeds/chemistryABSTRACT
In this work, we newly synthesized granular composite (GASA) via hydrothermal treatment of polyaluminum chloride (PAC) and subsequently granulation pelleting with starch gel as an organic binder. The resulting composite was characterized with analytic instruments, and the feasibility of utilizing GASA as adsorbent for the removal of fluoride (F-) was tested in the batch and column experiments. The characterization results revealed that GASA possessed a spherical/porous framework consisting of aluminosilicate (i.e., ordered albite, NaAlSiO3O8). The results of final pH effect experiments and XRD/XPS analyses showed the dominant adsorption mechanisms of F- on GASA were electrostatic attraction by protonated surface Al-OH, ligand exchange between surface hydroxyl groups and F ions, and surface precipitation (i.e., cryolite formation). Based on the results of adsorption kinetics and adsorption isotherm, granulation resulted in the relatively slow kinetics of F adsorption compared to the powder type, but was preferred to retain good adsorption capacity. The regeneration possibility of GASA was also proven with the adsorption/desorption cyclic test. In the column study, 15-cm length of the GASA layer and the flow rate less than 0.85 mL min-1 were proposed to keep the satisfactory level of F in water. The experimental results offer a potential of PAC sludge-derived composite as adsorbent for the removal of F from water.
Subject(s)
Aluminum Hydroxide/chemistry , Water Pollutants, Chemical/chemistry , Water Purification/methods , Adsorption , Fluorides , Hydrogen-Ion Concentration , Kinetics , Sewage , Sodium Fluoride , Water , Water Pollutants, Chemical/analysisABSTRACT
A numerical flow analysis for the design of an oxidation pond was conducted to investigate the optimal flow characteristics. This analysis includes the inflow rate and the shape and depth of the oxidation pond. The total area and maximum depth of the pond were 500 m(2) and 3 m, respectively. We defined the retention time, retention time ratio, homogeneity index, and inflow exchange efficiency in order to choose the optimal conditions. The optimum width to length ratio and depth of the pond were found to be 1:5 and 2 m, respectively.
Subject(s)
Fresh Water , Oxidation-Reduction , Water PurificationABSTRACT
The objective of this study was to assess the changes in mine water quality as an underground mine flooded from July 2005 to October 2008. The effect of air injection with a blower into the water was used to evaluate the potential to convert ferrous to ferric iron and to provide in situ treatment and precipitation. Mine flooding averaged 31 cm/day with a linear shape until November 2007, when it flattened out due to outflow. During flooding, mine water pH remained around 6, but Eh shifted from 200 to -150 mV. After the mine water level stabilized, contents of elements such as Fe and SO(4) tended to decrease as time passed. Air was injected by diffusers (150 L/min/each) at three different depths of 2, 3, and 5 m below the water level in the shaft. Dissolved oxygen eventually increased to 4 or 5 mg/L depending on the depth of the diffusers. Aeration caused conversion of ferrous iron to ferric iron and about 30 mg/l of iron was removed from the mine water. Therefore, air injection shows potential as a semi-active treatment or part of conventional treatment to precipitate iron in the mine pool.
Subject(s)
Coal Mining , Environmental Monitoring/methods , Water/chemistry , Iron/chemistry , Rain , Seasons , Time Factors , Water Pollutants, Chemical/chemistryABSTRACT
This study was carried out to evaluate longevity of available organic materials used for sulfate-reducing bacteria (SRB) activity in vertical flow ponds (VFPs) to treat mine drainage in South Korea. Spent mushroom compost samples (SMC) were tested as substrates in VFPs and analyzed for total organic carbon in VFPs, and were collected to analyze total organic carbon (TOC), T-N, T-P, K, metals and residual cellulose to check the longevity assessment. Chemical analysis revealed that the average contents of Fe, Al and Mn in SMC of VFPs were 19,907, 32,137 and 434 mg/kg, respectively. The contents of Fe and Al in SMC of VFPs were much higher than those of the unused SMC (control), but to the contrary, those of Mn showed a reversed tendency. Average TOC content of the controls was 64.19% but in one of the VFP substrates was as low as 15.92%. This might be resulted from SRB consumed the available organic carbon in SMC as VFPs system aged. Contents of T-N in VFPs tended to decrease as VFPs aged. The residual cellulose ranged from 3.88 to 6.72% (g/g). There existed a negative relationship between residual cellulose contents and ages of VFPs. Assuming that SMC in all VFPs had similar compositions when the VFPs were initially established, trend analysis predicted that the amount of carbon source for SRB might be available for 12-15 years further, depending on VFPs.
Subject(s)
Biodegradation, Environmental , Bioreactors/microbiology , Mining , Organic Chemicals/metabolism , Water Pollutants, Chemical/metabolism , Agaricales/chemistry , Agaricales/metabolism , Carbon/analysis , Carbon/metabolism , Cellulose/analysis , Metals/analysis , Metals/metabolism , Organic Chemicals/analysis , Ponds , Republic of Korea , Sulfur/metabolism , Sulfur-Reducing Bacteria/metabolism , Waste Disposal, Fluid , Water Pollutants, Chemical/analysisABSTRACT
The cadmium (Cd) content of rice grain grown in metal-contaminated paddy soils near abandoned metal mines in South Korea was found to exceed safety guidelines (0.2 mg Cd kg⻹) set by the Korea Food and Drug Administration (KFDA). However, current remediation technologies for heavy metal-contaminated soils have limited application with respect to rice paddy soils. Laboratory and greenhouse experiments were conducted to assess the effects of amending contaminated rice paddy soils with zerovalent iron (ZVI), lime, humus, compost, and combinations of these compounds to immobilize Cd and inhibit Cd translocation to rice grain. Sequential extraction analysis revealed that treatment with the ameliorants induced a 50-90% decrease in the bioavailable Cd fractions when compared to the untreated control soil. When compared to the control, Cd uptake by rice was decreased in response to treatment with ZVI + humus (69%), lime (65%), ZVI + compost (61%), compost (46%), ZVI (42%), and humus (14%). In addition, ameliorants did not influence rice yield when compared to that of the control. Overall, the results of this study indicated that remediation technologies using ameliorants effectively reduce Cd bioavailability and uptake in contaminated rice paddy soils.