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Heteroaggregation of Graphene Oxide with Nanometerand Micrometer-Sized Hematite Colloids: Influence on Nanohybrid Aggregation and Microparticle Sedimentation Yiping Feng, Xitong Liu, Khanh An Huynh, J. Michael McCaffery, Liang Mao, Shixiang Gao, and Kai Loon Chen Environ. Sci. Technol., Just Accepted Manuscript • Publication Date (Web): 15 May 2017 Downloaded from http://pubs.acs.org on May 20, 2017

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Environmental Science & Technology

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Heteroaggregation of Graphene Oxide with Nanometer- and

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Micrometer-Sized Hematite Colloids: Influence on Nanohybrid

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Aggregation and Microparticle Sedimentation

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Revised manuscript submitted to:

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May 7, 2017

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Yiping Feng,1, 2, 3, *, Xitong Liu,1, Khanh An Huynh,4 J. Michael

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McCaffery,5 Liang Mao,2 Shixiang Gao,2 and Kai Loon Chen1

⊥

1

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Department of Environmental Health and Engineering, Johns Hopkins University, Baltimore, Maryland 21218-2686, United States

State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, Jiangsu 210023, China 3

Institute of Environmental Health and Pollution Control, School of Environmental Science and Engineering, Guangdong University of Technology, Guangzhou 510006, China

4

5

Faculty of Environment and Natural Resources, Ho Chi Minh City University of Technology, Ho Chi Minh City, Vietnam

The Integrated Imaging Center, Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218-2686, United States

* Corresponding author: Yiping Feng, E-mail: [email protected], Phone: 86-20-39322547.

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ACS Paragon Plus Environment


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Abstract

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Heteroaggregation of graphene oxide (GO) with nanometer- and micrometer-sized

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hematite colloids, which are naturally present in aquatic systems, is investigated in this

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study. The heteroaggregation rates between GO and hematite nanoparticles (HemNPs)

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were quantified by dynamic light scattering, while the heteroaggregation between GO

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and micrometer-sized hematite particles (HemMPs) was examined through batch

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adsorption and sedimentation experiments. The heteroaggregation rates of GO with

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HemNPs first increased and then decreased with increasing GO/HemNP mass

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concentration ratios. The conformation of GO–HemNP heteroaggregates at different

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GO/HemNP mass concentration ratios was observed through transmission electron

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microscopy imaging. Initially, GO underwent heteroaggregation with HemNPs through

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electrostatic attraction to form primary heteroaggregates, which were further bridged by

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GO to form bigger clusters. At high GO/HemNP mass concentration ratios where GO

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outnumbered HemNPs, heteroaggregation resulted in the formation of stable GO–

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HemNP nanohybrids that have a critical coagulation concentration of 308 mM NaCl at

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pH 5.2. In the case of HemMPs, GO adsorbed readily on the microparticles and, at an

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optimal GO/HemMP ratio of ca. 0.002, the sedimentation of HemMPs was fastest, most

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likely due to the formation of “electrostatic patches” which led to favorable aggregation

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of the microparticles.

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Introduction

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Graphene oxide nanosheets (GO), due to their outstanding physicochemical

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properties,1, 2 are expected to have many potential applications.2-4 During the production

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and use of GO-containing consumer products as they enter the market (e.g., GO-based

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sensors for cancer detection, thermal paste for cooling CPU, and electrodes for lithium

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ion batteries),5-7 it is inevitable that GO will be released into the environment, possibly

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causing adverse impacts on human health and ecosystems.8-14 Due to their layered

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structure and the distribution of oxygen-containing functional groups on the basal planes

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and sheet edges,2, 15, 16 GO has excellent dispersibility and high mobility in the aqueous

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environment. Dispersed GO has been reported to have higher cytotoxicity than the

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aggregated ones because the dispersed nanosheets have more opportunities to interact

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with cells directly.11 Therefore, it is essential to investigate the aggregation behavior of

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GO in aquatic environments in order to have a better understanding about their impact

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and potential risk to human health and aquatic organisms.

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In natural waters, the concentration of GO is likely to be several orders of magnitude

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lower than the concentration of natural colloids.17, 18 Thus, the heteroaggregation of GO

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with natural colloids (e.g., metal oxides, clay particles, and macromolecular organic

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matter), rather than the homoaggregation of GO, is expected to be the dominant process

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that governs the fate and transport of GO.17-21 To date, only a few studies have focused

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on the heteroaggregation of GO in aquatic environments. Negatively charged GO has

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been observed to interact favorably with positively charged particles via electrostatic

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attraction.22-24 For example, Zhao et al.24 investigated the heteroaggregation of GO with

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different minerals through adsorption studies.

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irreversibly adsorbed to positively charged goethite, but not to negatively charged

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montmorillonite or kaolinite.24 Nevertheless, no research has been conducted to quantify

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the heteroaggregation rates between GO and natural colloids. In particular, the difference

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in the concentration ratio of GO to natural colloids in various environmental settings

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(such as high ratio near the point where GO-containing wastewater is discharged and

3

The authors found that GO was



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lower ratio downstream in the river) can result in different heteroaggregation rates

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between GO and natural colloids. In addition, the heteroaggregation between GO and

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HemNPs can lead to the formation of GO-HemNP nanohybrids, the colloidal stability of

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which remains largely unknown. Moreover, it is expected that the wide size distribution

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of natural colloids in natural waters (i.e., from nanometer to micrometer size range) can

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influence the stability of GO through different mechanisms.25 Therefore, the study of GO

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heteroaggregation at environmentally relevant conditions is needed in order to better

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understand and predict the environmental fate and transport of these nanosheets.

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The objective of this work is to investigate the heteroaggregation behavior of GO

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with nanometer- and micrometer-sized hematite particles (HemNPs and HemMPs,

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respectively), both chosen as representative natural colloids. The heteroaggregation rate

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of GO with HemNPs was determined over a broad range of GO/HemNP mass

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concentration ratios through time-resolved dynamic light scattering (DLS). The

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conformation of GO–HemNP heteroaggregates was directly observed under a

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transmission electron microscope (TEM). The effect of GO on the sedimentation of

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HemMPs was also investigated through sedimentation and batch adsorption experiments,

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as well as electrophoretic mobility measurements.

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heteroaggregation between GO and HemNPs or HemMPs for different mass

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concentration ratios were proposed based on our experimental results.

Finally, the mechanisms for

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Experiment Section

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Preparation of GO and Hematite Colloids. Single-layered GO nanosheets

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(SKU-GO-005) are purchased from Graphene Supermarket (Reading, MA). Details for

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the preparation of GO stock suspensions are provided in the Supporting Information (SI).

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Both hematite colloids, HemNPs and HemMPs, were synthesized through the forced

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hydrolysis of FeCl3.26, 27 The method used to synthesize hematite colloids is presented in

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SI.

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Characterization of GO and Hematite Colloids. The hydrodynamic diameters

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of GO and HemNPs in the stock suspensions were measured through DLS. These

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measurements were performed using a BI-200SM goniometer (Brookhaven, Holtsville,

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NY) equipped with a 488 nm argon laser at a scattering angle of 90°.28 The shape and

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size distribution of HemMPs were determined through TEM imaging (Philips EM 420

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TEM with an accelerating voltage of 100 kV). The electrophoretic mobilities (EPMs) of

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GO and hematite colloids were measured with a ZetaPALS analyzer (Brookhaven,

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Holtsville, NY) at 0.1 mM NaCl and pH 5.2 ± 0.2.

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Solution Chemistry. A NaCl stock solution was prepared by dissolving ACS-

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grade NaCl in deionized (DI) water (18 MΩ•cm, Milli-Q system, Millipore, MA) and

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then filtered through a 0.1-µm PVDF syringe filter (Millipore, MA). All aggregation

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experiments were performed at an unadjusted pH of 5.2 ± 0.2.

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Determination of Homoaggregation Kinetics and Heteroaggregation Rates.

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Time-resolved DLS measurements were used for the determination of homoaggregation

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kinetics and heteroaggregation rates. Homoaggregation kinetics of GO and HemNPs

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were determined to evaluate the stability of these nanomaterials under different

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concentrations of NaCl.

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efficiencies, α. Detail procedures for the determination of α29, 30 and critical coagulation

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concentrations (CCCs)31 of GO and HemNPs are presented in the SI.

Homoaggregation kinetics was quantified using attachment

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Heteroaggregation experiments between GO and HemNPs were performed at a

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constant HemNP concentration of 0.44 mg/L and at a NaCl solution of 0.1 mM (pH 5.2)

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using the method reported in our previous publication.32 This solution chemistry was

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chosen to avoid the homoaggregation of both GO and HemNP.32 In addition, the pH of

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5.2 lies within the typical pH range of 5–9 for most natural waters.33, 34 The HemNP

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concentration of 0.44 mg/L is representative of typical concentrations of iron in river

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waters.35, 36 GO concentrations were varied from 0.9 to 440.0 µg TOC/L to achieve the

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GO/HemNP mass concentration ratios in the range of 0.002–1.000.

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heteroaggregation rates of GO and HemNPs were determined through time-resolved DLS

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measurements. Notably, the scattered light intensity from the HemNP suspension (0.44

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mg/L) was significantly higher (> 18 times) than the intensities of the GO suspensions

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(0.9–440.0 µg TOC/L). During the process of heteroaggregation, the increase in the

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hydrodynamic diameter (Dh) was recorded over 5–60 min for the accurate derivation of

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the initial heteroaggregation rates. The linear regression of heteroaggregation rates was

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performed over a time period in which Dh,t reached 1.3 times of the initial hydrodynamic

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diameter of HemNPs, Dh,0. When the heteroaggregation was very slow (i.e., Dh,t failed to

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reach 1.3 Dh,0), the regression would be performed over a duration of 60 min. This

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approach to calculating the rates of aggregation has been employed in our previous

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publications.28, 30 In all cases, the y-intercepts of the fitted lines did not exceed 8 nm in

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excess of the initial hydrodynamic diameter of HemNPs (Dh,0 = 90 nm).29

The

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Homoaggregation Kinetics and EPMs of GO–HemNP Nanohybrids. GO and

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HemNP suspensions were mixed together at 0.1 mM NaCl and pH 5.2 to obtain a 10-mL

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GO–HemNP mixture containing 12.4 mg TOC/L GO and 1.24 mg/L HemNPs. GO and

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HemNPs were allowed to undergo heteroaggregation for 30 min. At these concentrations,

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the HemNPs were expected to be completely coated with GO to form GO–HemNP

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nanohybrids (to be discussed in Results and Discussion section). The suspension was

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then centrifuged at 3,650 g (Beckman Coulter, CA) for 1 h to separate the GO–HemNP

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nanohybrids from the suspension. The supernatant (90 % of total volume) was carefully

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decanted and replaced with an equal volume of deionized (DI) water (Millipore, MA).

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This cleaning process was repeated once.

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suspension was sonicated for 10 min in order to obtain a monodispersed nanohybrid

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suspension. The homoaggregation kinetics of these nanohybrids was determined as a

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function of NaCl concentration at pH 5.2 through time-resolved DLS.

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measurements, the nanohybrid suspension was diluted ca. 5 times with 0.1 mM NaCl

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solution, resulting in a GO concentration of 2.33 mg TOC/L and a HemNP concentration

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of 0.23 mg/L.

The obtained GO–HemNP nanohybrid

For EPM

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Sedimentation Rates of HemMPs and HemNPs in the Presence of GO. Due

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to the fast sedimentation associated with the large HemMPs (~ 2 µm), we were not able

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to perform DLS measurements on the HemMP suspensions.

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experiments were conducted on HemMPs under varying concentrations of GO to provide

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insights into the heteroaggregation behavior between HemMPs and GO.

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sedimentation of HemMPs was examined at 0.1 mM NaCl and pH 5.2.

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experiments, the HemMP concentration was fixed at 150 mg/L, while the GO

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concentrations were 0.00, 0.25, 4.00, and 8.00 mg TOC/L. Immediately after being

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prepared in polystyrene cuvettes (BI-SCP, Brookhaven), the GO–HemMP suspensions

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were mixed using a rotating disk (TC-7, New Brunswick Scientific, 30 rpm). After 30

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min of mixing, the absorbance values of the mixtures at a wavelength of 760 nm, at

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which the absorption of GO was negligible (Figure S1a), were recorded over 60 min

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using a UV–Vis spectrometer (UV-1800, Shimadzu, Japan). The adsorption of GO on

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HemMPs was also determined to elucidate its effects on the sedimentation of HemMPs.

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Instead, sedimentation

The

For these


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Detailed procedures of the adsorption experiments are provided in the SI.

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For the sedimentation experiments with HemNPs, 30 mg/L HemNP was mixed

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with varying concentrations of GO in polystyrene cuvettes.

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suspensions were mixed using a shaking incubator (1585, VWR) at 150 rpm for 20 min.

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Next, the cuvettes were placed in a UV-Vis spectrometer and the absorbance at 416 nm

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(where the contribution of GO to the total absorbance was insignificant) was recorded

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over 60 min to determine the sedimentation rates of HemNPs.

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Transmission Electron Microscopy.

The GO–HemNP

The conformation of GO–HemNP

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heteroaggregates formed at GO/HemNP mass concentration ratios of 0.004, 0.060, and

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0.400 was observed through TEM imaging (Philips EM 420).

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suspensions were prepared in the same solution chemistry as that used for

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heteroaggregation experiments (i.e., 0.1 mM NaCl and pH 5.2).

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heteroaggregation, 5–10 µL of heteroaggregate suspensions was deposited on carbon-

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coated copper TEM grids and the heteroaggregates were subsequently stained with 2%

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uranyl acetate solutions before imaging. Details on sample preparation can be found in

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the SI.

The heteroaggregate

After 15 min of

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Results and Discussion

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Homoaggregation of GO and HemNPs. The hydrodynamic diameters of the

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GO and HemNP stock suspensions were measured to be 125–149 nm and 87–95 nm,

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respectively. At 0.1 mM NaCl and pH 5.2, EPM measurements showed that GO was

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negatively charged and HemNPs were positively charged (Figure 1a). The ionization of

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the carboxylic groups on GO is primarily responsible for the negative surface charge of

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GO at this solution chemistry.1, 37 HemNPs were positively charged at pH 5.2 due to the

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dominance of –OH2+ surface functional groups (isoelectric point = 9.3).27

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FIGURE 1 Homoaggregation kinetics of GO and HemNPs were systematically examined

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over a wide range of NaCl concentrations.

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HemNPs, which were calculated from their respective aggregation profiles (Figure S2),

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increased with increasing NaCl concentrations before reaching a maximum value at the

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CCC. The attachment efficiencies of GO and HemNPs at different NaCl concentrations

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were shown in Figure 1b. The distinct reaction-limited (α < 1) and diffusion-limited (α =

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1) regimes indicate that the homoaggregation of GO and HemNPs is qualitatively in

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agreement with DLVO theory.30, 31 The CCCs of GO and HemNP were 221.6 and 45.8

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mM NaCl, respectively, indicating that both nanoparticles are stable to homoaggregation

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at 0.1 mM NaCl, the salt concentration at which the GO–HemNP heteroaggregation

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experiments were conducted.

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The homoaggregation rates of GO and

Heteroaggregation Rates of GO with HemNPs.

At 0.1 mM NaCl, the

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homoaggregation of GO and HemNPs was inhibited by strong electrostatic repulsion

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(Figure S3).

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concentration ratio of 0.06, the hydrodynamic diameter measured from this mixture

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significantly increased, indicating that heteroaggregation between the oppositely charged

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GO and HemNPs occurred favorably (Figure S3). Similar observations were made in our

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earlier studies on the heteroaggregation between HemNPs and multiwalled carbon

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nanotubes (MWCNTs),32,

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nanoparticles.39

However, when GO were mixed with HemNPs at GO/HemNP mass

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and also between HemNPs and citrate-coated silver

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Figure 2a shows representative GO–HemNP heteroaggregation profiles obtained

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at GO/HemNP mass concentration ratios of 0.000–0.400. The heteroaggregation rates

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obtained over a wide range of GO/HemNP mass concentration ratios are shown in Figure

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2b.

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heteroaggregation was very slow and the heteroaggregation rate was even lower than the

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maximum HemNP homoaggregation rate under diffusion-limited conditions (ca. 0.07

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nm/s, indicated by dashed line in Figure 2b). As the GO/HemNP ratio was gradually

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increased from 0.006 to 0.090, the heteroaggregation rate increased correspondingly.

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The maximum heteroaggregation rate (0.40 nm/s) was obtained at the optimal

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GO/HemNP ratio of 0.090 and this rate was ca. 5 times higher than the maximum

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homoaggregation rate of HemNPs. As the GO/HemNP ratios were further increased

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above 0.090, the heteroaggregation rate continually decreased until it approached zero at

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GO/HemNP ratios of 0.400 and higher.

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It is apparent that at extremely low GO/HemNP ratios (0.002–0.004),

FIGURE 2 TEM Imaging of Heteroaggregates.

TEM was employed to observe the

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conformation of GO–HemNP heteroaggregates at low, near optimal, and high

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GO/HemNP mass concentration ratios. In the following discussion, small, intermediate,

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and big heteroaggregates are defined as heteroaggregates containing 1–3, 4–8, and > 8

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HemNPs, respectively. Figure 3 shows representative TEM images of different sized

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GO–HemNP heteroaggregates, all formed at a GO/HemNP mass concentration of 0.06

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after ca. 15 min of heteroaggregation. It was generally observed that one GO can bind

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with either one or several HemNPs to form a primary heteroaggregate.40 These primary

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heteroaggregates were then bridged together by GO to form bigger clusters. It is worth

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nothing that some HemNPs were observed to be in contact with one another in Figure 3.

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It is possible that GO, with the flexible sheet and large surface area, can bridge several

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HemNPs close together despite the electrostatic repulsion between them.

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FIGURE 3

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The distributions of heteroaggregates comprising between 1 and > 8 HemNPs per

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heteroaggregate were determined at GO/HemNP mass concentration ratios of 0.004,

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0.060, and 0.400 (Figure 4).

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concentration ratios were 82, 130, and 142, respectively. At the low GO/HemNP ratio of

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0.004, more than 80 % of heteroaggregates were small and most HemNPs did not

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undergo heteroaggregation with GO. This observation was in agreement with our DLS

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results, which showed that HemNPs remained relatively stable in the presence of low GO

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concentrations (around several µg TOC/L).

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percentage of small heteroaggregates decreased (< 35 %) while the percentages of

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intermediate and big heteroaggregates increased. This change in the heteroaggregate size

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distribution indicated that GO underwent significant and rapid heteroaggregation with

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HemNPs, which was also consistent with the DLS results (Figure 2b).

The numbers of heteroaggregates examined at these

At the GO/HemNP ratio of 0.060, the

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FIGURE 4

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At the high GO/HemNP ratio of 0.400 (Figure 4), small heteroaggregates again

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became dominant while intermediate and big heteroaggregates were rarely observed (
8 4-8 1-3

80 60 40 20 0

0.004

0.06

0.4

GO/HemNP Ratio

Figure 4. Size distributions of heteroaggregates at different GO/HemNP mass concentration ratios. More than 80 heteroaggregates were observed for each concentration ratio.

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1.0

GO/HemMP Ratio 0 0.0017 0.027 0.053

C/C0

0.8 0.6 0.4 0.2 0.0

(a) 0

10

20

30

40

50

60

Time (min) 1.0

C/C0

0.8 0.6 GO/HemNP Ratio

0.4

0 0.001 0.01 0.3

0.2 0.0

(b) 0

10

20

30

40

50

60

Time (min) Figure 5. Sedimentation of (a) HemMPs and (b) HemNPs in the absence and presence of GO at 0.1 mM NaCl and pH 5.2. Absorbance of the HemMP and HemNP suspensions was measured at 760 and 416 nm, respectively.

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1.4

(a)

Incubation Time (hour) 0.25 48

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q (mg/g)

1.0 0.8 0.6 0.4 0.2

(b)

4 2

-8

2

EPM (10 m /Vs)

0.0

0 -2 -4

0

1

2

3

4

5

GO Concentration (mg/L) Figure 6. (a) Adsorption of GO on HemMPs at 0.1 mM NaCl and pH 5.2 at incubation times of 15 min and 48 hours. (b) Electrophoretic mobility (EPM) measurements of GO mixed with HemMPs at 0.1 mM NaCl and pH 5.2. The dashed line represents the EPM of GO. Error bars represent the standard deviations from triplicate experiments.

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Heteroaggregation of Graphene Oxide with ... - ACS Publications

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