Bioavailability of Carbon Nanomaterial-Adsorbed Polycyclic Aromatic

Jul 12, 2017 - Department of Civil and Environmental Engineering, University of Massachusetts Lowell, Lowell Massachusetts 01854, United States...
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Bioavailability of carbon nanomaterial-adsorbed polycyclic aromatic hydrocarbons to P. promelas: influence of adsorbate molecular size and configuration Erica N. Linard, Onur G Apul, Tanju Karanfil, Peter van den Hurk, and Stephen J. Klaine Environ. Sci. Technol., Just Accepted Manuscript • DOI: 10.1021/acs.est.7b02164 • Publication Date (Web): 12 Jul 2017 Downloaded from http://pubs.acs.org on July 12, 2017

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Bioavailability of carbon nanomaterial-adsorbed polycyclic aromatic hydrocarbons to P. promelas: influence of adsorbate molecular size and configuration †, ‡

*Erica N Linard, Klaine

, Onur G Apul

§,a

||

, Tanju Karanfil , Peter van den Hurk

†,#

, and Stephen J.

†,^



Institute of Environmental Toxicology, Clemson University, Pendleton, South Carolina, USA



Interdisciplinary Graduate Program in Environmental Toxicology, Clemson University

§

School of Sustainable Engineering and the Built Environment, Arizona State University,

Tempe, AZ a

Department of Civil and Environmental Engineering, University of Massachusetts Lowell,

Lowell MA ||

Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson,

South Carolina, USA # ^

Department of Biological Sciences, Clemson University, Clemson, South Carolina, USA Deceased

KEYWORDS. Bioavailability, adsorption, carbon nanomaterials, polycyclic-aromatic hydrocarbons, bioavailability index 1

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ABSTRACT. Despite carbon nanomaterials’ (CNMs) potential to alter the bioavailability of

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adsorbed contaminants, information characterizing the relationship between adsorption behavior

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and bioavailability of CNM-adsorbed contaminants is still limited. To investigate the influence

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of CNM morphology and organic contaminant (OC) physicochemical properties on this

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relationship, adsorption isotherms were generated for a suite of polycyclic aromatic

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hydrocarbons (PAHs) on multi-walled carbon nanotubes (MWCNTs) and exfoliated graphene

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(GN) in conjunction with determining the bioavailability of the adsorbed PAHs to Pimphales

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promelas using bile analysis via fluorescence spectroscopy. Although it appeared that GN

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adsorbed PAHs indiscriminately compared to MWCNTs, the subsequent bioavailability of GN-

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adsorbed PAHs was more sensitive to PAH morphology than MWCNTs. GN was effective at

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reducing bioavailability of linear PAHs by ~ 70%, but had little impact on angular PAHs.

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MWCNTs were sensitive to molecular size, where bioavailability of two-ringed naphthalene was

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reduced by ~80%, while bioavailability of the larger PAHs was reduced by less than 50%.

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Furthermore, the reduction in bioavailability of CNM-adsorbed PAHs was negatively correlated

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with the amount of CNM surface area covered by the adsorbed-PAHs. This study shows that the

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variability in bioavailability of CNM-adsorbed PAHs is largely driven by PAH size,

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configuration and surface area coverage.

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ABSTRACT ART.

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INTRODUCTION. Among the numerous applications carbon nanomaterials (CNMs) are used

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for, CNMs’ high adsorption affinity for organic contaminants (OCs) has led to increasing interest

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in such materials for pollution remediation.1,2 However, due to CNMs’ unique physicochemical

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characteristics, they interact with OCs in a distinctly different way than natural colloids.

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Considerable uncertainty exists pertaining to CNMs’ potential to facilitate transport of adsorbed

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contaminants and likewise alter bioavailability of adsorbed contaminants in the environment.3-6

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Adsorption capacity and rate of desorption from CNMs are considered the most influential

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properties driving contaminant transport and likely influence bioavailability of CNM-adsorbed

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molecules.5,7

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Several studies have found that CNM type and OC properties significantly impact

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bioavailability of CNM-adsorbed contaminants, though findings are not conclusive.7-9 Xia et al.

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found the bioaccumulation of aliphatic perfluorochemicals (PFCs) in C. plumosus was mainly

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driven by PFC structure rather than type of CNM.9 Similarly, the bioavailability and toxicity of

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phenanthrene adsorbed to five different types of carbon nanotubes (CNTs) in D. magna was not

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significantly different despite differences in CNTs’ surface area, functionalization and

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diameter.10 Conversely, studies have observed phenanthrene to become more bioaccessible as

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CNMs surface curvature decreases and with increased dispersion. 7,9,11,12 The bioaccumulation of

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several classes of aromatic OCs, including polycyclic aromatic hydrocarbons (PAHs),

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polychlorinated biphenyls (PCBs), and polybrominated diphenyl ethers (PBDEs) in benthic

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invertebrates was more effectively moderated when sediment was amended with CNTs than

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black soot; this was attributed to higher adsorption affinity for OCs by CNTs.13 Although

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without inclusion of adsorption data it was not possible to discern how carbonaceous material

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type contributed to differences in OC bioaccumulation. While the bioavailable fraction of CNM-

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adsorbed contaminants is often assumed to be directly related to the un-adsorbed OC 3

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concentration in the system, bioaccumulation enhancement of diuron and ionizable

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pentachlorophenol indicate this may not necessarily be the case.14,15 By examining how OC-

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CNM interactions and adsorption behavior is linked with resulting bioavailability of the adsorbed

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contaminant, a more holistic understanding of how CNMs may act as a “contaminant carrier”

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can be established.

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Although CNTs are essentially graphene sheets rolled into tubes and graphene has

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become increasingly popular, few studies exist investigating the influence of graphene on

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bioavailability of adsorbed contaminants. Adsorption of OCs by graphene and CNTs is largely

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driven by hydrophobic forces and π-π bonding16,17, but due to different interactions with

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adsorbates, graphene and CNTs can have different adsorption mechanisms.18,19 To the best of our

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knowledge, no study exists examining how such differences in adsorption interactions of

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graphene and CNTs may differentially affect bioavailability of adsorbed contaminants.

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Therefore, the main objectives of this study were to (i) compare adsorption of four OCs by

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exfoliated graphene (GN) and multi-walled carbon nanotubes (MWCNTs), (ii) investigate the

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role of OC physicochemical characteristics on adsorption interaction differences between the two

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materials, and (iii) compare the impact of GN and MWCNT on OC bioavailability to Pimphales

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promelas as a function of adsorption behavior, in environmentally relevant conditions. PAHs

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were selected as a model class of OCs for this study because they are ubiquitous in the

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environment, on the EPAs priority pollutant list, and have a wide range of physicochemical

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properties.

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MATERIALS AND METHODS

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Chemicals and particles. Multi-walled carbon nanotubes (MWCNTs) were purchased

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from Nanostructured & Amorphous Materials (Houston, TX) and mechanically exfoliated

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graphene (GN) was prepared at Clemson University. Details on the characterization techniques 4

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are described in the Supplemental Information (SI) and Table S1 summarizes CNMs’

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morphological characteristics. Four polycyclic aromatic hydrocarbons (PAHs) were used in this

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study: naphthalene (NAP), 99+% purity, from Alfa Aesar; phenanthrene (PHEN), 97% purity,

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and anthracene (ANT), 99% purity from ACROS organics; fluoranthene (FLU), 98% purity,

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from ULTRA scientific. Physicochemical properties of PAHs are presented in Table S2. Stock

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solutions were prepared in HPLC grade methanol. Suwannee River natural organic matter

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(NOM) collected from Suwannee River Visitor’s Center (Fargo, GA) had a dissolved organic

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carbon concentration of 64 mg C/L, determined using a Shimadzu total organic carbon analyzer

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and had a specific ultraviolet absorbance (SUVA254) value of 4.08 L mg-1m-1. All solutions were

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prepared in moderately hard water following the U.S. Environmental Protection Agency standard

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recipe; 96 mg/L NaHCO3, 60 mg/L CaSO4, 60 mg/L MgSO4, 4 mg/L KCl in 18 mega-ohm

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Millipore Milli-Q water.

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Suspension of CNM. Pristine MWCNTs and GN were suspended in 2 mg C/L NOM at a

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concentration of 10 mg/L following previously published methods.20 CNMs were sonicated for 1

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hour at 60 watts using a 0.5 microtip affixed Branson model 450 digital sonifier. Mass based

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calibration curves of MWCNTs and GN in solution are supplied in Supplemental Information

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(Figure S2); concentration was measured via visible light absorbance at 800 and 660 nm for

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MWCNT and GN solutions respectively, using a Molecular Devices Spectramax 190 microplate

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spectrophotometer.21,22 CNM solutions were diluted to ~1.5 mg/L in 2 mg C/L NOM background

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solution for all adsorption and bioavailability assays. Absorbance measurements of CNM

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solutions at beginning and end of each experiment showed little change in concentration,

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indicating a stable solution.

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Adsorption Isotherms. Adsorption experiments were run in triplicate following the

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batch approach we have previously published.20 Briefly, 10 mL glass centrifuge tubes containing 5

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either 1.5 mg/L MWCNT or GN suspension was spiked with each PAH individually, sealed with

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aluminum-foil-lined Teflon screw caps and allowed to come to equilibrium on a rotary tumbler

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at room temperature (25ºC± 1°C) for 96 hours (preliminary tests showed that equilibrium was

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reached within 48 hours). PAH stock solutions used to spike experimental vials were prepared so

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that the volume percentage of methanol was 0.1% to avoid co-solvent effects. Initial PAH

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concentrations of NAP, PHEN, ANT and FLU ranged from 5-1000, 5-400, 0.25-40, and 1-200

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µg/L, respectively. Vials without CNMs were identically prepared to serve as positive controls;

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controls for the entire system were spiked with methanol only. A combination of centrifugation

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and fluorescence quenching techniques were used to quantify the un-adsorbed PAH

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concentration left in the system. After equilibrium was reached vials with and without CNM

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were centrifuged (Eppendorf 5804 R) at ~1500 x g for 1 hour to sediment any CNM

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agglomerates that may have formed during tumbling. The remaining supernatant was analyzed in

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black polystyrene 96-well plates with Molecular Devices Gemini fluorescence microplate reader

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at excitation/emission wavelengths 276/330, 252/399, 250/363, and 280/440 for NAP, ANT,

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PHEN and FLU respectively. PAHs act as π-donors when interacting with graphitic materials

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and when adsorbed no longer are in an excited state. Therefore, fluorescence of CNM-adsorbed

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PAHs is statically quenched and the remaining unbound PAH concentration in the aqueous

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solution could be determined via fluorescence intensity.23-25 Analysis of a methanol rinse of

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positive control vials showed minimal loss of PAHs due to sorption to vial walls. CNM sorption

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of all PAHs was calculated as differences in aqueous PAH concentration between positive

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controls and CNM samples using fluorescent standard curves developed for each PAH in the

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background solution containing 2 mg/L NOM. Temperature, pH, and ionic strength were

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controlled across each experiment and reflected minimal change. The adsorption data was fit

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with the nonlinear Freundlich model (model details presented in the SI). 6

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Bioavailability Assays. All exposures were conducted for 16 h in static, non-aerated

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conditions with full water renewals every 4 h (refer to SI for details on background conditions).

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Assays assessing the influence of MWCNT and GN on PAH bioavailability to P. promelas were

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replicated four times where each aquarium was stocked with ~4 fish per treatment. Response of

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fish from each aquarium were averaged to represent a single experimental unit per replicate per

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treatment. The prepared treatments for each PAH were 1) control, consisting of background

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solution only; 2) PAH only, a positive control consisting of PAH-spiked background solution

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(i.e. 10 µg/L of NAP, PHEN and FLU; 5 µg/L of ANT); and 3) PAH and CNM, consisting of the

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same PAH-spiked background solution with either ~1.5 mg/L of suspended MWCNT or GN.

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Solutions for each treatment were tumbled in 4L amber glass containers on a rotary tumbler to

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reach equilibrium prior to fish exposure. Water samples from each exposure were collected at the

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beginning and end of each water renewal; analysis of water samples verified the treatment PAH

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concentrations throughout duration of the exposure. At the end of each exposure, fish were

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euthanized, the gallbladder harvested, and the collected bile analyzed for PAH metabolites to

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determine the bioavailable fraction of PAH in the system.

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Bioavailability is defined as the total amount of PAH that is taken up by the organism

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from the system and biotransformed26,27; including aqueous and CNM-adsorbed PAH exposure.

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Due to highly efficient metabolism of PAHs by fish, the bioaccumulation potential of these

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compounds in traditionally monitored tissues such as muscles is typically low and not always

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well correlated with exposure.28 Instead, PAHs are quickly biotransformed into water-soluble

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metabolites in the liver and concentrated in the gallbladder for later excretion. Most PAHs have

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distinct fluorometric properties allowing for easy detection and identification in complex

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matrices like bile.28 Dose-response relationships showed a linear correlation between PAH

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exposure and bile fluorescence intensity (Figure S3), therefore change in bile fluorescence was 7

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directly related to change in PAH bioavailability. Extracted bile was diluted, vortexed, and

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centrifuged. The supernatant was analyzed via fixed wavelength fluorescence (FF) analysis at

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discreet excitation and emission wavelength pairs for each PAH.28,29 PHEN, ANT, and FLU

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metabolites were detected using a Molecular Devices Gemini fluorescence microplate reader at

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excitation/emission wavelengths of 250/363, 252/399, and 280/440 nm; NAP metabolites were

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detected via HPLC with a UV-fluorescence detector 276/330 nm. See SI for more details on bile

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preparation and analysis.

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Statistical Analysis. JMP Pro 12 software, SAS Institute Inc. was used to perform all

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statistical tests. Adsorption isotherms were fit with the non-linear Freundlich model. Multiple

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regression was used to assess and compare the influence of PAH physicochemical characteristics

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on adsorption of PAHs by CNMs. Linear regression and correlation coefficients (R2) were used

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to assess goodness of fit of predicted fish responses to actual response in fish exposures and

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CNM bioavailability assays. Analysis of variance (ANOVA) followed by Student’s T test were

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used to compare response of fish across all treatments for a single PAH; linear squared contrasts

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were used to compare differences between treatments across the different PAHs. Two-tailed

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mean hypothesis testing was used to determine whether bioavailability indices differed from 1

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for each PAH_CNM combination. Student’s T test was used to compare bioavailability indices

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to one another across all PAHs. Shapiro-Wilk’s test was used to test normality of bile

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fluorescence residuals; Brown and Forsythe test was used to test homogeneity of variance within

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treatments. Unless otherwise denoted, the significance level of all tests was set at 0.05.

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RESULTS AND DISCUSSION

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Influence of CNM type on adsorption. Adsorption isotherms of PAHs by MWCNT and

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GN in the presence of 2 mg C/L NOM are represented in the form of a distribution curve

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following methods by Zhu et al., where adsorption (qe) of the PAHs by GN was plotted against 8

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the adsorption of the PAHs by MWCNT at the same experimental concentration (Figure 1).30

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The corresponding Freundlich parameters of individual adsorption isotherms are on Table 1. To

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help conceptualize differences in GN/MWCNT distribution among the four PAHs, lines at 0.33,

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1 and 3 are provided on Figure 1 to represent GN/MWCNT distribution coefficients (KGN/MWCNT)

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where qGN = 0.33 qMWCNT, qGN = qMWCNT, or qGN = 3qMWCNT, respectively. On a mass basis,

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distribution coefficients of PHEN and FLU fall along 0.33 distribution line (Figure 1 [A]) though

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NAP and ANT fall closer to the distribution line equal to one. Further comparison of the

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Freundlich KF values confirms that MWCNT adsorption capacity for FLU and PHEN was

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significantly greater (p-value