scholarly journals The Influence of Ionic and Nonionic Surfactants on the Colloidal Stability and Removal of CuO Nanoparticles from Water by Chemical Coagulation

2019 ◽  
Vol 16 (7) ◽  
pp. 1260 ◽  
Author(s):  
Rizwan Khan ◽  
Muhammad Inam ◽  
Sarfaraz Khan ◽  
Andrea Jiménez ◽  
Du Park ◽  
...  
Keyword(s):  
Natural Waters ◽  
Colloidal Stability ◽  
Pure Water ◽  
Copper Oxide Nanoparticles ◽  
Consumer Products ◽  
Hydrodynamic Diameter ◽  
Lauryl Sulfate ◽  
Nonylphenol Ethoxylate ◽  
Cuo Nps ◽  
Treatment Processes

The widespread use of copper oxide nanoparticles (CuO NPs) and surfactants in various consumer products makes it likely that they coexist in aqueous environments, making it important to study the effects of surfactants on the fate and transport behavior of CuO NPs. The present study aims to investigate the influence of anionic sodium lauryl sulfate (SLS) and nonionic nonylphenol ethoxylate (NPEO, Tergitol NP-9), on CuO NPs adsorption, aggregation, and removal from water by the coagulation process. The result of the sorption study indicates that both surfactants could be adsorbed on the surface of CuO NPs, and that SLS remarkably decreases the ζ potential as well as the hydrodynamic diameter (HDD) of CuO as compared to NP-9. The kinetic aggregation study showed that both SLS and NP-9 reduced the HDD of CuO NPs and retarded the settling rates at surfactant concentrations above 0.015% (w:v) over a 24 h-period. Moreover, enhanced aggregation of CuO NPs was observed in two environmental waters as compared to pure water, which could be related to their high ionic strength. The addition of surfactants in natural waters has been shown to reduce the aggregation and sedimentation of CuO; however, the reductive effect of SLS was more pronounced than that of NP-9. Finally, the coagulation results showed that the removal efficiencies of CuO, Cu2+, and the surfactant in all tested waters at optimum ferric chloride dosage reached around 98, 95, and 85%, respectively. Furthermore, the coagulation mechanism revealed that the combination of charge neutralization and adsorptive micellar flocculation (AMF) might be involved in the removal of both pollutants. The results of the present study provide new insight into the environmental behavior of coexisting NPs and surfactants in wastewater treatment processes.

scholarly journals Removal of ZnO Nanoparticles from Natural Waters by Coagulation-Flocculation Process: Influence of Surfactant Type on Aggregation, Dissolution and Colloidal Stability

2018 ◽  
Vol 11 (1) ◽  
pp. 17 ◽  
Author(s):  
Rizwan Khan ◽  
Muhammad Inam ◽  
Muhammad Iqbal ◽  
Muhammad Shoaib ◽  
Du Park ◽  
...  
Keyword(s):  
Natural Waters ◽  
Colloidal Stability ◽  
Sodium Dodecyl ◽  
Sustainable Use ◽  
Freundlich Isotherm ◽  
Hydrodynamic Diameter ◽  
Zno Nps ◽  
Nonylphenol Ethoxylate ◽  
Treatment Processes ◽  
Coagulation Mechanism

The zinc oxide nanoparticles (ZnO NPs) and surfactants that are widely used in commercial and industrial products lead to the likelihood of their co-occurrence in natural water, making it essential to investigate the effect of surfactants on the fate and mobility of ZnO NPs. The present study seeks to elucidate the effect of an anionic sodium dodecyl sulfate (SDS) and a nonionic nonylphenol ethoxylate (NPEO), on ZnO NPs adsorption, aggregation, dissolution, and removal by the coagulation process. The results indicate that the presence of SDS in ZnO NPs suspension significantly reduced the ζ-potential and hydrodynamic diameter (HDD), while the effect of NPEO was found not to be significant. The sorption of SDS and NPEO by ZnO NPs were fitted with Langmuir model, but the Freundlich isotherm was more suitable for SDS at pH 9.0. Moreover, the adsorption was strongly pH-dependent due to the formation of mono-bilayer patches onto the NPs. The SDS remarkably affect the dissolution and aggregation phenomena of ZnO NPs in natural waters as compared to NPEO. Finally, the coagulation results showed that the removal efficiency of ZnO, Zn2+ and the surfactant in synthetic and wastewaters at optimum ferric chloride (FC) dosage reached around 85–98% and 20–50%, respectively. Coagulation mechanism investigation demonstrated that the cooperation of charge neutralization and adsorptive micellar flocculation (AMF) might play an important role. In summary, this study may provide new insight into the environmental behavior of coexisting ZnO NPs and surfactants in water treatment processes, and it may facilitate their sustainable use in commercial products and processes.

Dissolution of metal and metal oxide nanoparticles under natural freshwater conditions

2015 ◽  
Vol 12 (2) ◽  
pp. 138 ◽  
Author(s):  
Niksa Odzak ◽  
David Kistler ◽  
Renata Behra ◽  
Laura Sigg
Keyword(s):  
Ionic Strength ◽  
Food Packaging ◽  
Natural Waters ◽  
Metal Oxide Nanoparticles ◽  
Treatment Plant ◽  
Low Ph ◽  
Consumer Products ◽  
Water Type ◽  
Cuo Nps ◽  
Low Ionic Strength

Environmental context Engineered nanomaterials (e.g. silver, zinc oxide and copper oxide) are being widely used in many consumer products such as cosmetics, food packaging and textiles. During their usage and treatment, they will be released to natural waters and partly dissolve, depending on the water type and nanomaterial characteristics. These nanomaterials may thus have some toxic effects to aquatic organisms and indirectly to humans because of higher concentrations of dissolved silver, zinc and copper in natural waters. Abstract The dissolution of some widely used nanoparticles (NPs), Ag (citrate coated), ZnO, CuO and Cu-carbon coated (Cu/C), has been studied over a period of 9 days in five different natural waters: wastewater treatment plant effluent (WWTP Dübendorf) and lakes Greifen, Lucerne, Gruère and Cristallina. These waters differ in ionic strength, pH and dissolved organic carbon (DOC). The dissolved fraction of metals from NPs was determined using DGT (diffusion gradients in thin films) and ultrafiltration (UF). ZnO-NPs and CuO-NPs dissolved to a large extent in all waters, whereas the dissolved fraction was much smaller in the case of Cu/C and Ag-NPs. All NPs dissolved to a larger extent in water from Lake Cristallina with low pH, low ionic strength and low DOC. Ag-NP dissolution was favoured at low ionic strength and low pH, whereas dissolution of CuO-NPs was mostly dependent on pH. Cu/C-NPs strongly agglomerated and sedimented and yielded low dissolved Cu concentrations. DGT and UF produced similar results, although these two methods differ in the measurement time scale. The results of this study indicate that dissolution is an important process for these NPs under conditions of natural waters or wastewaters.

scholarly journals The Removal of CuO Nanoparticles from Water by Conventional Treatment C/F/S: The Effect of pH and Natural Organic Matter

Molecules ◽  
2019 ◽  
Vol 24 (5) ◽  
pp. 914 ◽  
Author(s):  
Rizwan Khan ◽  
Muhammad Ali Inam ◽  
Du Ri Park ◽  
Sarfaraz Khan ◽  
Muhammad Akram ◽  
...  
Keyword(s):  
Organic Matter ◽  
Natural Organic Matter ◽  
Colloidal Stability ◽  
Copper Oxide Nanoparticles ◽  
Engineered Nanoparticles ◽  
Cuo Nps ◽  
Effects Of Ph ◽  
Alkaline Conditions ◽  
Ft Ir ◽  
The Fourier Transform

The increased use of engineered nanoparticles (ENPs), such as copper oxide nanoparticles (CuO NPs), in commercial products and applications raises concern regarding their possible release into freshwater sources. Therefore, their removal from water is important to eliminate adverse environmental and human health effects. In this study, the effects of pH and natural organic matter (NOM), i.e., humic acid (HA) and salicylic acid (SA) on the removal of CuO NPs by coagulation/flocculation/sedimentation (C/F/S) were evaluated. The results indicated that pH significantly affects the coagulation efficiency, where 10–60% CuO NPs removal was achieved under extreme acidic/alkaline conditions. However, at neutral pH, removal of up to 90% was observed with a lower ferric chloride (FC) dosage (0.2 mM). The coagulation efficiency and mechanism were strongly affected by the type of Fe species present in the aqueous phase, which is mainly controlled by pH. Higher concentrations of both HA and SA decrease the CuO NPs agglomeration rate, and thereby improve the colloidal stability due to the NOM molecules adsorbed onto the NPs surface. The presence of hydrophobic HA needs a higher FC dosage of 0.5–0.8 mM than a dosage of hydrophilic SA of 0.25–0.35 mM, to obtain a similar CuO coagulation efficiency. Moreover, higher removals of dissolved organic carbon (DOC) and UV254 were observed more in hydrophobic NOM than in hydrophilic. The results of the Fourier transform infrared (FT-IR) analysis of FC composite flocs confirm that the charge neutralization and enmeshment of coagulant might be a possible removal mechanism. The findings of the current study may provide critical information in the prediction of the fate, mobility, and removal of CuO NPs during C/F/S in water treatment.

scholarly journals Influence of Organic Ligands on the Colloidal Stability and Removal of ZnO Nanoparticles from Synthetic Waters by Coagulation

Processes ◽  
2018 ◽  
Vol 6 (9) ◽  
pp. 170 ◽  
Author(s):  
Rizwan Khan ◽  
Muhammad Inam ◽  
Du Park ◽  
Saba Zam Zam ◽  
Sookyo Shin ◽  
...  
Keyword(s):  
Large Scale ◽  
Natural Waters ◽  
Colloidal Stability ◽  
Removal Rate ◽  
Engineered Nanoparticles ◽  
Organic Ligands ◽  
Hydrodynamic Diameter ◽  
Scale Production ◽  
Excess Charge ◽  
Zno Nps

The large-scale production and usage of zinc oxide nanoparticles (ZnO NPs) may lead to their post-release into the aquatic environment. In this study, the effect of hydrophobic/hydrophilic organic ligands on sorption and sedimentation of ZnO NPs has been systematically investigated. In addition, the coagulation efficiency of ZnO NPs, Zn2+, dissolved organic carbon (DOC), and UV254 with varying ferric chloride (FC) dosages in synthetic waters were also evaluated. The results showed that the higher concentration of organic ligands, i.e., humic acid (HA), salicylic acid (SA), and L-cysteine (L-cys) reduced the ζ-potential and hydrodynamic diameter (HDD) of particles, which enhanced the NPs stability. The adsorption of organic ligands onto ZnO NPs was fitted with the Langmuir model, with maximum adsorption capacities of 143, 40.47, and 66.05 mg/g for HA, SA and L-cys respectively. Removal of up to 95% of ZnO NPs and Zn2+ was achieved in studied waters at the effective coagulation zone (ECR), above which excess charge induced by coagulant restabilized the NPs in suspension. Moreover, the removal rate of DOC and UV254 were found to be higher in hydrophobic waters than hydrophilic waters. The width of ECR strongly depends on the characteristics of source water. The waters with hydrophobic ligand and higher UV254 values require more coagulant than hydrophilic waters to achieve the similar ZnO NPs and Zn2+ removal. The results of Fourier transform infrared (FT-IR) analysis of ZnO NPs composite contaminant flocs indicated that the combined effect of enmeshment and charge neutralization might be a possible removal mechanism. These findings may facilitate the prediction of fate, transport, and removal of ZnO NPs in the natural waters, and might contribute to risk assessment, as well as decision making about engineered nanoparticles (ENPs) in aquatic systems.

Silver nanoparticle removal from drinking water: flocculation/sedimentation or filtration?

2013 ◽  
Vol 13 (5) ◽  
pp. 1181-1187 ◽  
Author(s):  
Desmond F. Lawler ◽  
Anne M. Mikelonis ◽  
Ijung Kim ◽  
Boris L. T. Lau ◽  
Sungmin Youn
Keyword(s):  
Silver Nanoparticles ◽  
Drinking Water ◽  
Organic Matter ◽  
Natural Organic Matter ◽  
Conventional Treatment ◽  
Granular Media ◽  
Natural Waters ◽  
Consumer Products ◽  
Treatment Processes ◽  
Water Treatment Plants

Silver nanoparticles are used in a wide variety of consumer products and are therefore rapidly becoming ubiquitous in the natural environment; they can be expected to be found in the natural waters used as drinking water supplies. This research investigated whether such particles could be expected to be removed in conventional water treatment plants such as flocculation and filtration. Both flocculation and granular media filtration experiments with citrate-capped silver nanoparticles were performed at different ionic strengths and in the presence and absence of natural organic matter. The results were generally consistent with theories of particle destabilization that have been developed for larger particles (greater than 1 μm), suggesting that silver nanoparticles are likely to be removed in conventional treatment processes.

scholarly journals Interaction between Persistent Organic Pollutants and ZnO NPs in Synthetic and Natural Waters

Nanomaterials ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 472 ◽  
Author(s):  
Rizwan Khan ◽  
Muhammad Inam ◽  
Sarfaraz Khan ◽  
Du Park ◽  
Ick Yeom
Keyword(s):  
Polybrominated Diphenyl Ethers ◽  
Natural Waters ◽  
Colloidal Stability ◽  
Aquatic Organisms ◽  
Hydrodynamic Diameter ◽  
Zno Nps ◽  
Ζ Potential ◽  
Diphenyl Ethers ◽  
Ft Ir ◽  
Aromatic Ether

The use of zinc oxide nanoparticles (ZnO NPs) and polybrominated diphenyl ethers (PBDPEs) in different products and applications leads to the likelihood of their co-occurrence in the aquatic system, making it important to study the effect of PBDPEs on the fate and transport of ZnO NPs. In this study, we determine the influence of PBDPEs (BDPE-47 and BDPE-209) on the colloidal stability and physicochemical properties of ZnO NPs in different aqueous matrices. The results indicated the shift in ζ potential of ZnO NP from positive to negative in the presence of both PBDPEs in all tested waters; however, the effect on the NPs surface potential was specific to each water considered. The lower concentration of the PBDPEs (e.g., 0.5 mg/L) significantly reduced the ζ potential and hydrodynamic diameter (HDD) of ZnO NP, even in the presence of high content of dissolved organic matter (DOM) in both freshwater and industrial wastewater. Moreover, both BDPE-47 and BDPE-209 impede the agglomeration of ZnO NP in simple and natural media, even in the presence of monovalent and polyvalent cations. However, the effect of BDPE-47 on the ζ potential, HDD, and agglomeration of ZnO NP was more pronounced than that of BDPE-209 in all tested waters. The results of Fourier transform infrared (FT-IR) and X-ray Photon Spectroscopy (XPS) further confirm the adsorption of PBDPEs onto ZnO NP surface via aromatic ether groups and Br elements. The findings of this study will facilitate a better understanding of the interaction behavior between the ZnO NPs and PBDPEs, which can reduce the exposure risk of aquatic organisms to both pollutants.

scholarly journals Concurrent Synthesis of Zero- and One-Dimensional, Spherical, Rod-, Needle-, and Wire-Shaped CuO Nanoparticles by Proteus mirabilis 10B

2018 ◽  
Vol 2018 ◽  
pp. 1-14 ◽  
Author(s):  
Marwa Eltarahony ◽  
Sahar Zaki ◽  
Desouky Abd-El-Haleem
Keyword(s):  
Proteus Mirabilis ◽  
Colloidal Stability ◽  
Copper Oxide Nanoparticles ◽  
Antagonistic Activity ◽  
One Dimensional ◽  
Gram Positive Bacteria ◽  
Cuo Nps ◽  
Vis Spectroscopy ◽  
Global Biogeochemical Cycles ◽  
Biomimetic Nanomaterials

Natural environment is a wealthy source of bionanofactories that invested in green approaches as the fabrication of biomimetic nanomaterials. The current study points out the importance of microbial activity in metal bioremediation, green synthesis of NPs, and global biogeochemical cycles of bioactive metals as well. It describes for the first time the synchronous biosynthesis of zero- (intracellular) and one-dimensional (extracellular) copper oxide nanoparticles (CuO-NPs) via Proteus mirabilis 10B. This bionanofactory represents key location of reduction and stabilization, and its exopolysaccharide additionally provides nucleation and growth site for CuO-NPs. The as-synthesized CuO-NPs were characterized; UV-Vis spectroscopy revealed surface plasmon resonance at 275 and 430 nm for intracellular and extracellular CuO-NPs, respectively. XRD reflected crystalline, pure phase monoclinic structure CuO-NPs. EDX illustrated strong copper signal with atomic percentages 32.3% (intracellular) and 14% (extracellular) CuO-NPs. However, ζ-potential recorded −62.5 and −43.8 mV with PDI 0.207 and 0.313 for intracellular and extracellular CuO-NPs, respectively, confirming the colloidal stability and monodispersity. Moreover, TEM micrographs depicted quasi-spherical intracellularly sequestered CuO-NPs (10 nm). Unexpectedly, extracellular CuO-NPs exhibited rod-, needle-, and wire-shaped with 17–37.5 nm in width and 112–615 nm in length. The antagonistic activity of both types of CuO-NPs was evaluated against Gram-negative and Gram-positive bacteria (aerobic and anaerobic), biofilm, yeast, mold, and algae. The potent antagonistic efficacy of CuO-NPs was displayed which encourages its utilization in controlling microbial contamination. Finally, the promising metabolic activity of Proteus mirabilis 10B can be exploited in simultaneous and beneficial applications for human and the surrounding ecosystem.

ANTIBIOTIC PROFILE AND ANTIBACTERIAL ACTIVITY OF COPPER OXIDE NANOPARTICLES AGAINST Pseudomonas fluorescens ISOLATED FROM WOUND INFECTION

2019 ◽  
Vol 9 (o3) ◽  
Author(s):  
Haider Qassim Raheem ◽  
Takwa S. Al-meamar ◽  
Anas M. Almamoori
Keyword(s):  
Antibacterial Activity ◽  
Copper Oxide ◽  
Pseudomonas Fluorescens ◽  
Wide Spectrum ◽  
Copper Oxide Nanoparticles ◽  
Morphological Properties ◽  
Clinical Samples ◽  
Oxide Nanoparticles ◽  
Cuo Nps ◽  
Disk Diffusion Assay

Fifty specimens were collected from wound patients who visited Al-Hilla Teaching Hospital. The samples were grown on Blood and MacConkey agar for 24-48 hr at 37oC. The bacterial isolates which achieved as a pure and predominant growth from clinical samples as Pseudomonas fluorescens, were identified using morphological properties and Vitek2 system. The anti-bacterial activity of copper oxide nanoparticles (CuO NPs) against was tested by (disk diffusion assay) using dilutions of (400, 200, 100, 50, 25, and 12.5‎µ‎g/ml). The (MIC and MBC) of each isolate was determined. CuO NPs shows wide spectrum antibacterial activity against tested bacteria with rise zone of inhibition diameter that is proportionate with the increase in nanoparticle concentration. The MIC of CuO NPs extended from 100-200‎µ‎g/ml and the MBC ranged from 200-400‎µ‎g/ml. The antibiotic profile was determined by Viteck 2 compact system (Biomérieux). CuO NPs‎ found highly effective and safe in P. fluorescens wounds infections comparing with used antibiotics.

A Facile Synthesis of Cu2O and CuO Nanoparticles Via Sonochemical Assisted Method

2018 ◽  
Vol 15 (2) ◽  
pp. 209-213 ◽  
Author(s):  
Sathish Mohan Botsa ◽  
Ramadevi Dharmasoth ◽  
Keloth Basavaiah
Keyword(s):  
Diffuse Reflectance Spectroscopy ◽  
Cupric Oxide ◽  
Copper Acetate ◽  
Chemical Properties ◽  
Copper Oxide Nanoparticles ◽  
Reducing Agents ◽  
Sonochemical Method ◽  
Phase Purity ◽  
X Ray ◽  
Cuo Nps

Background: During past two decades, functional nanomaterials have received great attention for many technological applications such as catalysis, energy, environment, medical and sensor due to their unique properties at nanoscale. However, copper oxide nanoparticles (NPs) such as CuO and Cu2O have most widely investigated for many potential applications due to their wide bandgap, high TC, high optical absorption and non-toxic in nature. The physical and chemical properties of CuO and Cu2O NPs are critically depending on their size, morphology and phase purity. Therefore, lots of efforts have been done to prepare phase CuO and Cu2O NPs with different morphology and size. Method: The synthesis of cupric oxide (CuO) and cuprous oxide (Cu2O) NPs using copper acetate as a precursor by varying the reducing agents such as hydrazine sulphate and hydrazine hydrate via sonochemical method. The phase, morphology and crystalline structure of a prepared CuO and Cu2O NPs were investigated by X-ray diffraction (XRD), Fourier transform infrared (FTIR), Field emission scanning electron microscopy (FESEM), Energy dispersive X-ray (EDS) and UV-Visible Diffuse reflectance spectroscopy (DRS). Results: The phase of NPs was tuned as a function of reducing agents.XRD patterns confirmed the formation of pure phase crystalline CuO and Cu2O NPs. FTIR peak at 621 cm-1 confirmed Cu(I)-O vibrations, while CuO vibrations confirmed by the presence of two peaks at 536 and 586 cm-1. Further investigation was done by Raman, which clearly indicates the presence of peaks at 290, 336, 302 cm-1 and 173, 241 cm-1 for CuO and Cu2O NPs, respectively. The FESEM images revealed rod-like morphology of the CuO NPs while octahedral like shape for Cu2O NPs. The presence of elemental Cu and O in stoichiometric ratios in EDS spectra confirms the formation of both CuO and Cu2O NPs. In summary, CuO and Cu2O NPs were successfully synthesized by a sonochemical method using copper acetate as a precursor at different reducing agents. The bandgap of CuO and Cu2O NPs was 2.38 and 1.82, respectively. Furthermore, the phase purity critically depends on reducing agents.

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