Figures
Abstract
Biosorption with macroalgae is a promising technology for the bioremediation of industrial effluents. However, the vast majority of research has been conducted on simple mock effluents with little data available on the performance of biosorbents in complex effluents. Here we evaluate the efficacy of dried biomass, biochar, and Fe-treated biomass and biochar to remediate 21 elements from a real-world industrial effluent from a coal-fired power station. The biosorbents were produced from the freshwater macroalga Oedogonium sp. (Chlorophyta) that is native to the industrial site from which the effluent was sourced, and which has been intensively cultivated to provide a feed stock for biosorbents. The effect of pH and exposure time on sorption was also assessed. These biosorbents showed specificity for different suites of elements, primarily differentiated by ionic charge. Overall, biochar and Fe-biochar were more successful biosorbents than their biomass counterparts. Fe-biochar adsorbed metalloids (As, Mo, and Se) at rates independent of effluent pH, while untreated biochar removed metals (Al, Cd, Ni and Zn) at rates dependent on pH. This study demonstrates that the biomass of Oedogonium is an effective substrate for the production of biosorbents to remediate both metals and metalloids from a complex industrial effluent.
Citation: Kidgell JT, de Nys R, Hu Y, Paul NA, Roberts DA (2014) Bioremediation of a Complex Industrial Effluent by Biosorbents Derived from Freshwater Macroalgae. PLoS ONE 9(6): e94706. https://doi.org/10.1371/journal.pone.0094706
Editor: Tilmann Harder, University of New South Wales, Australia
Received: January 7, 2014; Accepted: March 18, 2014; Published: June 11, 2014
Copyright: © 2014 Kidgell et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This research is part of the MBD Energy Research and Development program for Biological Carbon Capture and Storage with the co-operation of Stanwell Energy Corporation. This project is supported by the Advanced Manufacturing Cooperative Research Centre (AMCRC), funded through the Australian Government's Cooperative Research Centre Scheme, and the Australian Renewable Energy Agency (ARENA). Stanwell Energy Corporation provided effluents for the study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: We have the following interests. This research is part of the MBD Energy Research and Development program for Biological Carbon Capture and Storage with the co-operation of Stanwell Energy Corporation. Stanwell Energy Corporation provided effluents for the study. The data contained within this study form a component of Australian Provisional Patent AU2013902101: “Biosorbent and methods of use”, James Cook University. There are no further patents, products in development or marketed products to declare. This does not alter our adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.
Introduction
Mining, mineral processing and energy generation produce large quantities of contaminated effluent. For example, coal-fired power stations produce complex effluents containing dissolved elements from the flushing of ash from the flue and furnace [1]. The resulting effluent contains elements at concentrations of potential environmental concern, such as Al, As, B, Cd, Mo, Se, Sr, V, and Zn, and extensive treatment is required before the effluent can be discharged [1], [2]. As the cost and operational conditions of treatment options can be prohibitive [1], [3], the effluent is often retained in large storages known as Ash Dams (AD). However, despite the apparent confinement of these water bodies, AD remain a significant source of toxic elements to local organisms [4]. Consequently, there is a need for a cost effective, sustainable and comprehensive approach to the remediation of complex industrial effluents.
Biosorption with biomass is an alternative to existing waste water treatment technologies with promising results at the laboratory scale [5]. Biosorption exploits the ability of dead or denatured biomass, such as dried macroalgae, to passively bind ions from aqueous solutions [6], [7]. Dried macroalgae are particularly effective biosorbents due to the high abundance of functional groups which have a strong affinity for dissolved cationic metals despite also having relatively high concentrations of these same metals in the biomass [8]. Many functional groups can be involved in biosorption and this can vary according to taxonomic groupings. For example, in brown algae the carboxylic groups of alginates are typically dominant in biosorption processes, while some freshwater green algae, such as Oedogonium, have cellulosic cell walls that resemble those of higher plants [9], [10]. These functional groups can passively bind dissolved metals through various processes, including passive electrostatic attraction, ion exchange with “light” metal ions (Ca2+, Na+, K+ and Mg2+), or complexation processes [10].
Macroalgae (and other biosorbents such as activated carbon) only have an affinity for dissolved cations and are relatively ineffective at treating oxyanions, such as selenate (SeO42−) that are common constituents of effluents [11]. However, dried macroalgae can be manipulated to improve its affinity for specific contaminants. Biomass can be converted to carbon-rich biochar through slow pyrolysis, resulting in a product with similar properties to activated carbon [12]. Additionally, biomass and biochar can be pre-treated with an iron (Fe) solution to improve the adsorption of anionic metalloids, including SeO42− [13]. Deposition of Fe onto the surface of either dried biomass or biochar provides a positive charge, promoting the formation of inner-sphere complexes between oxyanionic metalloids and Fe-treated biosorbents, where there would otherwise be no natural affinity for sorption [14]–[16].
Despite the promise of macroalgae as a biosorbent, industrial application has been limited. One key factor limiting the application of biosorption is the lack of a sustainable and sufficient source of biomass [6], [17]. Wild harvests of biomass to support biosorption are simply not sustainable when one considers the volumes required [6], and commercially cultivated seaweeds have existing applications in other markets [17]. However, in recent work we have shown that native species of macroalgae can be cultured to provide sustainable biomass for bioremediation [17], [18]. This cultivated biomass represents a sustainable source of biomass, but little research has considered the efficacy of cultivated biomass in biosorption applications.
An additional limitation of existing biosorption research is that it has focused on simple synthetic effluents. These studies often focus on the kinetics of sorption and the mechanisms of uptake of select elements under idealized conditions. In contrast, real-world industrial effluents are complex, involving multiple interacting and competing contaminants that occur in a variety of speciation and oxidation states, which are influenced by environmental conditions [2], [8]. Biosorption research that has been conducted in multi-element systems has shown that non-target elements can interfere with [19], [20] or competitively exclude [21] biosorption of target elements. Consequently, in multi-element systems the capacity of a biosorbent for individual elements typically decreases in comparison to results obtained in idealized single-element effluents [22]. Macroalgal biosorbents have not yet been proven to be an effective means of treating complex effluents with multiple co-existing contaminants [7] and it is rare for studies to consider systems with more than three elements [8]. In fact, very little is known about the performance of biosorbents of any type in multi-elemental systems, or the effects that physical parameters such as pH and exposure time have in these scenarios.
Here we address key constraints to the industrial application of algal-based biosorption by assessing the efficacy of a macroalgal biosorbent for use in a real-world complex industrial effluent. We collect a native isolate of the cosmopolitan freshwater macroalgal genus Oedogonium (Link ex Hurn, 1900) from the AD of a coal-fired power station and cultivate it in intensive production systems as a means of providing sustainable biomass for biosorption. Specifically, we test Oedogonium dried biomass, derived biochar, Fe-treated biomass and Fe-treated biochar as biosorbents for 21 metals and metalloids in an effluent taken from coal-fired power production under a range of pH conditions and exposure times. These results will establish the potential of biosorption for the remediation of complex industrial effluents using purposely cultivated biomass.
Materials and Methods
Industrial effluent
This study targeted Ash Dam Water (ADW) from Tarong coal-fired power station in south-east Queensland, Australia (26.76°S, 151.92°E). Tarong is one of Queensland's largest power stations with a generation capacity of 1400 MW, and a 46,000 ML AD storing contaminated waste water. ADW was sourced directly from the AD and transported to James Cook University (JCU), Townsville in 1000 L Intermediate Bulk Containers (IBCs) in November 2012. The ADW was then stored at ambient temperature in 12,000 L storage tanks until use. The effluent was collected and transported to JCU by Stanwell Energy Corporation.
Algal biosorbent production & preparation
Oedogonium sp. (Genbank: KF606974) [23] hereafter Oedogonium, was used as the source biomass for the production of biosorbents (see below). Oedogonium is a native filamentous, freshwater green alga in the Tarong AD [18]. Oedogonium samples were initially collected from the Tarong AD in October 2012 but could not be identified to species using taxonomic keys based on morphological characteristics [24]. The species was therefore assessed using molecular techniques, arguably the most accurate means to identify cryptic species, and this isolate has been assigned the Genbank accession number KC606974 with no current matches for this species in the database [23].
After collection from Tarong AD, Oedogonium was cultivated in Manutec f/2 algal growth media in 2500 L tanks during the austral summer months (January – March) in the aquaculture facility at JCU (19.33°S, 146.76°E). Prior to experiments, 2 kg of algae was harvested from the tanks and oven dried to a constant mass at 60°C for 48 hours (h). Subsequently, 1 kg of the dried Oedogonium biomass was converted into biochar by slow pyrolysis under conditions previously developed for macroalgae [12]. Briefly, Oedogonium was suspended within a muffle furnace (Labec CEMLS-1200) and continuously purged with N2 (BOC) gas at 4.0 L min−1 while being heated to a hold temperature of 450°C for 1 h. Additionally, a sub-sample of both the dried biomass and biochar were also treated with a 5% Fe solution, prepared by diluting FeCl3 (Sigma Aldrich 45% w/v) in deionized (DI) water (Millipore Direct-Q3), to become Fe-loaded biosorbents. Dried biomass and biochar were exposed to separate Fe solutions at a density of 25 g L−1 for 24 h on a shaker plate (100 rpm) at 20°C, then filtered from the solutions and rinsed three times with DI water at a rate of 20 ml g−1, then dried at 60°C for 48 h.
Biosorption experiments
Biosorption experiments were conducted to quantify the rate and composition of metal and metalloid adsorption from ADW by Oedogonium dried biomass, biochar, Fe-treated dried biomass and Fe-treated biochar at three alternate initial pH levels (2.5, 4, 7.1 see below). Filtered (0.45 µm sterile Starstedt syringe filters) samples of ADW were analyzed prior to experimental treatments to serve as a benchmark for initial conditions.
Two solutions of pH-manipulated ADW were produced with 1 M HCl (pH 2.5 and 4, Sigma Aldrich TraceSelect Ultra), while a third remained at the native pH of the ADW, 7.07±0.01. The experiment was fully factorial in design, with independent samples being destructively sampled at each time point. Each of the treatments consisted of a plastic beaker with 60 ml of ADW and 0.6 g of biomass, biochar or the Fe-treated derivatives (10 g L−1 of biosorbent). The beakers were shaken (100 rpm at 20°C) in incubator shaker cabinets. At the end of the allocated exposure time (0:15, 0:30, 1:00, 4:00, 24:00, or 168:00 hours) the samples were removed from the cabinets and filtered with 75 µm nylon filter paper. The solution was then filtered to 0.45 µm using a glass fiber filter and syringe, then analysed as described below. Samples containing no biosorbent were processed in the same manner to serve as negative controls to quantify losses of elements to experimental glassware and filtration. The experiment was replicated three times. All plastic and glassware was acid washed in a 5% HNO3 (Sigma Aldrich) bath for 48 h, then rinsed in DI water prior to use.
Elemental analysis
The concentrations of Al, As, Ba, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Se, Sr, V and Zn were measured with a Bruker 820-MS Inductively Coupled Plasma Mass Spectrometer (ICP-MS), and Ca, K, Mg and Na with a Varian Liberty series II Inductively Coupled Plasma Optical Emissions Spectrometer (ICP-OES). An external calibration strategy was used for both instruments, where a standard solution of 0.45 µm filtered ADW was used as the vector to calculate the concentration of elements. Collisional Reaction Interface (CRI) was used for As (H2) and V (He), while 82Se isotope was used for Se quantification, to eliminate polyatomic interferences for these elements. A 1% HCl solution was spiked with 1 ppb As, Se and V and measured three times for quality control; recovery between 98.5 and 110% indicated no significant interferences. All analyses were conducted at the Advanced Analytical Centre at JCU, Townsville.
Data analysis
Multivariate patterns in biosorption were visualized using Principal Components Analysis (PCA) from a correlation matrix with some elements log-transformed to create a normal distribution [25]. Univariate analysis took the form of three-way fully-factorial Analysis of Variance (ANOVA), with the factors biosorbent (fixed), pH (fixed) and time (random). Data were examined for normality and homogeneity of variance using normal-probability plot of raw residuals and predicted-residual scatter plot, and were transformed as necessary to meet assumptions [26]. Both the PCA and ANOVA test were conducted in Statistica for Windows (Ver. 10, C. Statsoft Inc. 1984–2011).
Results
Characteristics of ADW
Twelve (Al, As, B, Cd, Cr, Cu, Pb, Mn, Mo, Ni, Se and Zn) of the 21 elements measured in the ADW have trigger levels established by the Australian and New Zealand Environmental Conservation Council (ANZECC) [27]. Of these twelve elements, eleven (Al, As, B, Cd, Cr, Cu, Pb, Mo, Ni, Se and Zn) were in excess of the trigger values (Table 1). Given that these elements have quantifiable remediation goals they are the focus of the following results section.
Biochar, biomass and ANZECC metals
Biochar was the most effective biosorbent, removing a broad suite of metals (Mn, Al, Cr, Cu, Cd, Ni, Pb and Zn). from solution (Figures 1 and 2). The PCA shows that effluent treated by biochar clustered along the positive PC1 axis, being characterized by lower concentrations of metals than the effluents treated by the remaining biosorbents (Figure S1). There was, however, a significant effect of pH on the biosorption of most metals by biochar (“Biosorbent x pH” Table S1). At high initial pH (4.0 & 7.1) the raw biochar rapidly adsorbed metals from solution but at low initial pH (2.5), leached metals into solution (Figure 1a).
Biosorption of metals (Al, Cd, Cr, Cu, Pb, Mn, Ni, and Zn) by (a) biochar and (b) biomass and biosorption of metalloids (As, B, Mo and Se) by (c) Fe-biochar and (d) Fe-biomass. Initial pH of 2.5, 4 and un-manipulated (7.1) are shown by solid, dashed and dotted lines, respectively. Error bars show standard errors
Initial pH of 2.5, 4 and un-manipulated (7.1) are shown by solid, dashed and dotted lines, respectively. Error bars show standard errors. Horizontal dashed line indicates the respective ANZECC trigger concentration for each element.
Of the metals included in the ANZECC guidelines, Al, Ni and Zn were most effectively removed from solution by biochar, and each of these had a pH-dependent response in the rate of biosorption (Figure 2a, c, e; Table S1). All three of these metals were reduced below their respective ANZECC trigger levels by biochar at high initial pH, in the case of Al and Zn within 30 min (Table 1; Figure 2a, c, e). When pH was initially low (2.5), the concentration of Al and Zn increased in solution in the first 15 min, then over the next four hours adsorbed onto the biochar to finally reach levels below the limits of detection (Figure 2a, e). While Cd was also adsorbed by biochar at varying rates under different initial pH conditions (2.5, 4.0 and 7.1), it was not reduced to below the trigger level (Figure 2g; Table 1).
The response of metals to biomass varied greatly and, as with biochar, often in a pH-mediated fashion (Figure 1b). Overall, there was an increase in element concentrations in ADW treated with biomass (Figure 1b) which is supported by effluent treated by biomass being broadly distributed around the centroid in the PCA, demonstrating it was a relatively ineffective biosorbent (Figure S1). Al was the only metal reduced below its respective trigger level when exposed to biomass, and this only occurred at high initial pH (4 and 7.1) (Figure 2b). In contrast, at an initial pH of 2.5 the concentration of Al increased substantially and continuously for the entire exposure duration (Figure 2b). Again, Zn displayed a similar pattern (Figure 2f). When exposed to biomass, Ni and Cd both displayed a similar pattern of initial decrease in concentration at high pH (4.0 and 7.1) followed by no significant change for the remaining duration of exposure, however, in low initial pH (2.5) both Ni and Cd did not differ from the initial concentration (Figure 2d, h; Table S1). Mn displayed substantial pH-mediated leaching when exposed to both biochar and biomass (Figure. S3g, h).
Fe-biochar, Fe-biomass and ANZECC metalloids
Fe-biochar was an effective adsorbent of As, Mo and Se, and initial pH had no impact on the rate or extent of adsorption of these elements (Figure 1c, Table S1). The net concentration of all ANZECC oxyanionic metalloids (As, B, Mo, Se) decreased by 2700 µg L−1 (30%) within the first 15 min of exposure to Fe-biochar when the initial pH was 4 or 7.1 (Figure 1c). This can be visualized in the PCA, in which ADW treated with Fe-biochar clusters along the positive PC2 axis in the PCA, demonstrating the effluent treated with Fe-biochar tended to have lower concentrations of As, Se and Mo than the remaining treatments (Figure S1).
The concentrations of As, Mo and Se all dropped significantly lower with Fe-biochar than for any other biosorbent. As and Mo were adsorbed by Fe-biochar to below their respective trigger levels for all initial pH conditions (Table 1; Figure 3a, c). Se was substantially reduced within the first 15 mins by Fe-biochar but not to the point of the AZNECC trigger level (Figure 3e; Table 1). As and Mo followed the characteristic pattern of rapid initial adsorption within the first 15 mins and continued decline at a slower rate for the remaining exposure (Figure 3a, c). Initial concentrations of B were 20 times in excess of the trigger level and despite a drop in concentration of approximately 20% when exposed to Fe-biochar at an initial pH of 4 (Table 1), the concentration of B did not approach the trigger level for any of the treatments (Figure 3g, h).
Initial pH of 2.5, 4 and un-manipulated (7.1) are shown by solid, dashed and dotted lines, respectively. Error bars show standard errors. Horizontal dashed line indicates the respective ANZECC trigger concentration for each element.
Fe-biomass behaved in a similar manner to Fe-biochar, albeit not as successfully. There was an initial reduction of 1700 µg L−1 (18%) of ANZECC metalloids in the first 15 min of exposure to Fe-biomass (Figure 1c). Interestingly, untreated biomass at low pH (2.5) showed a similar total effectiveness with metalloids as Fe-biochar, with an initial decrease in metalloid concentration of 2400 µg L−1 (28%) in the first 15 min (Figure. S2d).Mo and Se were slightly reduced in ADW when exposed to Fe-biomass (Figure 3d, f; Table S1), however, these were the only elements to do so.
Discussion
This study demonstrates that the biomass of Oedogonium is an effective substrate for the production of biosorbents to remediate both metals and metalloids from a complex industrial effluent. Conversion of biomass to biochar through slow pyrolysis, and Fe-treatment of this biochar, produces biosorbents that effectively bind metals and metalloids respectively. The affinity of each biosorbent for different constituents of an extremely complex waste water effluent is clearly demonstrated where biochar binds metals from solution at a rate that is affected by pH, while Fe-biochar consistently binds metalloids from solution in a manner that is unaffected by pH. Our results therefore highlight the complexities of biosorption that are only apparent in experiments conducted on real-world industrial effluents. No single biosorbent was effective at holistically treating the range of elements in the complex ADW and so biosorption strategies for real-world effluents may require multiple stages of treatment.
The greatest change in metal and metalloid concentration within the ADW occurred in the first hour of exposure. Rapid initial sorption of metals and metalloids is commonly reported [28]–[33]. The effect of pH was pronounced for the untreated biosorbents, biomass and biochar, with biosorption patterns at low initial pH (2.5) often differing to those at higher initial pH (4.0 and 7.1). The effect of pH for Fe-biomass and Fe-biochar was, however, negligible. The pH-independent sorption of metalloids by Fe-treated biosorbents may be due to the formation of inner-sphere complexes [14], which are largely unaffected by ionic strength and act without the restrictions of electrostatic attraction, allowing bond formation irrespective of net biosorbent charge [34].
The suites of elements targeted by the most successful biosorbents, Fe-biochar and biochar, were distinct and complementary. Fe-biochar removed the oxyanionic metalloids As, Mo and Se, with As and Mo being reduced to below their respective ANZECC trigger levels, which is particularly notable for Mo as the concentration was initially 40 times in excess of the trigger level. While the ability of Iron Based Sorbents (IBS) to remediate anions has been established [11], [12], [13], [35], we have shown that the remediation of these metalloids in a complex effluent comes at the expense of substantial leaching of metals back into solution. Conversely, biochar was able to remove a suite of metals from solution and did not leach any ANZECC elements into solution at high pH. The ability to simultaneously remove multiple metals from solution makes biochar a very successful biosorbent in a multi-elemental context, and offers the potential to combine biochar and Fe-biochar in sequential treatment strategies to sequester both metals and metalloids from complex effluents.
For biochar, there was significant variation in metal sorption with half of the ANZECC metals (Al, Cu, Ni & Zn) being remediated to below their respective trigger levels, while metals such as Mn and K leached off the biochar and into solution. Ionic affinity for biosorbents is not fully understood, however, the ionic radius and electronegativity of a metal may have a significant effect [36]–[38]. For example, cation adsorption onto freeze-dried fungus Rhizopus arrhizus may be related to the electronegativity and ionic radius of each ion, otherwise known as the Covalent Index, which suggests Mn2+ has a very low sorption affinity [39], [40]. Consequently, it is possible that during this study ion exchange is occurring involving the release of Mn, with its relatively low affinity and high abundance on Oedogonium, in exchange for metals of higher affinity such as Zn, Pb or Cu [36].
Metals and metalloids behaved differently when exposed to biomass and biochar under low initial pH conditions. When exposed to biomass and biochar at an initial pH of 2.5, several metals (Al, Cd, Mn, Ni, Zn) had higher concentrations in solution than the higher pH (4 & 7.1) treatments. As described earlier, the biomass was initially sourced from Tarong Ash Dam and cultivated in f/2 media. Consequently, the resulting biomass contained elements from f/2 media that are required for growth and some of these elements leached when the dried biomass was returned to water at low pH (particularly Cu, Mo, Mn, Zn and Fe). Our finding that some elements leached from biomass at low pH further highlights the importance of measuring a broad suite of analytes in biosorption experiments to uncover unexpected interactions between target and non-target elements. Conversely, metalloids (Se, Mo and V) had lower concentrations at low initial pH. There are several possible explanations for this pH-mediated response. Firstly, the increased metal concentration is a result of increased availability of free-ions at lower pH [41], [42]. Second, the metals could be competitively excluded from the biosorption sites by the increased number of protons at lower pH [43], [44]. Third, the lowering of the pH below the isoelectric point of the biosorbent resulted in a net charge reversal and therefore enhanced the adsorption of metalloids while limiting the adsorption of metals [45]–[47]. In reality the pH-dependent adsorption of ions onto biosorbents is probably due to a combination of factors [6], [7]. Overall however, lowering the pH to 2.5 in this study had no benefit to the removal of ions as elements were most successfully removed from the effluent at an un-manipulated initial pH of 7.1.
Interestingly, when the biomass was converted to biochar, the metal leaching at low pH was reduced by more than 50%. While the behavior of complex feed stocks during slow pyrolysis is relatively poorly understood, it is known that biochar produced from element-rich biomass typically has a lower exchangeable fraction of metals than the feed stock. Some elements that are constituents of biomass are volatile and may not report to the biochar fraction during slow pyrolysis. Furthermore, converting biomass to biochar changes the speciation of bound metals, rendering them less liable to dissociation [48]. This is clearly supported by the significantly lower leaching of metals from biochar at low pH in our study. Clearly, therefore, biomass cultivated using f/2 media – or any similar growth media – can be considered an appropriate feedstock for biosorption despite containing elements that are also targets for bioremediation, and this biomass is most effective when converted to biochar and used at an unmodified pH.
In an overall sense, there is a developing dichotomy in the study of biosorption of metals and metalloids. The majority of research to date has focused on the kinetics and mechanisms of biosorption in synthetic effluents, which are in essence abstract and simplified conditions. While these studies are important in understanding the processes involved in biosorption, they lack the authenticity of complex effluents in which biosorption is to be applied [5]–[7]. Our results clearly demonstrate that macroalgae are a versatile feedstock for biosorbents, as Oedogonium biomass was able to be converted to biochar, Fe-biomass and Fe-biochar, each of which displayed differential affinity for metals and metalloids. Determination of whether the metal leaching that occurred for Fe-biochar (during the removal of the problematic metalloids) is an acceptable outcome or if the metals could be remediated using another process or biosorbent such as a sequential treatment, requires further investigation. A sequential approach in which alternative macroalgal-derived biosorbents are used in sequence on the same effluent solution, each targeting a specific suite of elements in the effluent, may result in a more comprehensive treatment. Regardless, our results highlight the critical importance of research that evaluates biosorbent performance in industrial effluents to fully understand the potential and viability of algal-based biosorption as a water treatment technology.
Conclusions
In conclusion we have not only demonstrated that the macroalga Oedogonium is an effective biosorbent in a complex industrial effluent, but we have done so with a macroalga that can be produced on-site at industrial facilities [18]. The biomass used in this study was cultivated at large scale in f/2 media to provide a rapidly growing source of biomass for waste water treatment in industry. To achieve this rapid growth, some elements must be added as part of any standard algal growth media, but these elements are minor components of the biomass relative to the positive effects of biosorption. The intensive cultivation of the biomass delivers the productivities required to support scaled biosorption which circumvents a critical barrier to application of biosorption. Furthermore, the on-site production of a native macroalga negates one of the most problematic components in the use of algal-based biosorbents, the source and transport of the biomass [6]. This offers a new paradigm in sustainable waste water treatment, where biomass for bioremediation is produced on-site at industrial facilities while delivering carbon capture. Through this strategic integration of industries, algal-based biosorption will have much greater prospects for industrial application.
Supporting Information
Figure S1.
Principal Components Analysis of solution concentration for 12 ANZECC elements. (A) PCA and (B) factor loadings for 12 elements include all biosorbent, time periods (excluding t0) and pH conditions, grouped by biosorbent. Vectors (factor loadings) indicate the direction and magnitude of correlation between a specific element and the biosorbent which resulted in the lowest respective concentration.
https://doi.org/10.1371/journal.pone.0094706.s001
(DOCX)
Figure S2.
The total respective biosorption of metals (Al, Cd, Cr, Cu, Pb, Mn, Ni, and Zn) by (a) Fe-biomass and (b) Fe-biochar and total respective biosorption of metalloids (As, B, Mo and Se) by (c) biochar and (d) biomass. Initial pH of 2.5, 4 and un-manipulated (7.1) are shown by solid, dashed and dotted lines, respectively. Error bars show standard errors.
https://doi.org/10.1371/journal.pone.0094706.s002
(DOCX)
Figure S3.
The biosorption of ANZECC metals (Pb, Cr, Cu, and Mn) when exposed to biochar and biomass. Initial pH of 2.5, 4 and un-manipulated (7.1) are shown by solid, dashed and dotted lines, respectively. Error bars show standard errors. Horizontal dashed line indicates the respective ANZECC trigger concentration for each element.
https://doi.org/10.1371/journal.pone.0094706.s003
(DOCX)
Table S1.
Three factor factorial Analysis of Variance tests run on each of the 12 ANZECC elements. Factorial analysis of variance tests were run on elemental concentration under the factors of Biosorbent, pH (Fixed) and Time (Random). Type III sum of squares was used. All tests met the assumption of homogeneity of variance, normality of residuals and independence. Transformation of the data were required for some elements, the transformation applied is listed next to the title. Factors in bold indicate significance under alpha of 0.05.
https://doi.org/10.1371/journal.pone.0094706.s004
(DOCX)
Acknowledgments
We thank Stanwell Energy Corporation for providing effluents for the experimental studies, and Charlotte Johansson, Thomas Mannering, Michael Bird and Tony Forsyth for their invaluable input and assistance.
Author Contributions
Conceived and designed the experiments: JK RN NP DR. Performed the experiments: JK. Analyzed the data: JK NP DR. Contributed reagents/materials/analysis tools: RN YH. Wrote the paper: JK RN NP DR. Chemical analyses: YH.
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