Anionic Polystyrene Research Articles

Topological control of polystyrene-silica core-shell microspheres

Controllable surface morphology is requisite across a gamut of processes, industries, and applications. The surface morphology of silica-coated polystyrene microspheres was controllably modified to enable generation of both smooth and bumpy, or raspberry-like, surfaces. Although smooth and raspberry-like silica shells on polystyrene templates have been demonstrated extensively, the method described here used readily available materials to produce radical changes in surface morphology from a single polystyrene template coated in silica through a facile sol-gel reaction processes. Silica shells were deposited via a sol-gel process (using tetraethyl orthosilicate as the silica precursor) onto 1 to 2 μm diameter anionic polystyrene spheres, fabricated by emulsifier-free polymerization. By varying the concentration of silica precursor and ammonium hydroxide catalyst and altering the electrostatic surface interactions via addition of a cationic polymeric brush, an array of surface topologies was generated. Incremented addition of the ammonium hydroxide base catalyst and sol-gel precursors generated smooth silica shells, whereas identical one-pot reactions led to raspberry-like shells. This modification of sol-gel deposition on large polystyrene cores via means of reactant addition offers additional control over sol-gel shell morphologies.

Enhanced Defluoridation Using Novel Millisphere Nanocomposite of La-Doped Li-Al Layered Double Hydroxides Supported by Polymeric Anion Exchanger

A novel nanocomposite bead LaLiAl-LDH@201 was fabricated by doping a small amount of La into nanocrystalline Li/Al layered double hydroxides (LDHs) pre-confined inside polystyrene anion exchanger D201 (LiAl-LDH@201). A systematic characterisation of the resultant LaLiAl-LDH@201 (XRD, SEM-EDS, TEM-EDS, and XPS) evidenced the successful incorporation of La into the Li/Al LDHs, with their interlayer distance expanded to allow more exchangeable sites for fluoride uptake. The resultant LaLiAl-LDH@201 showed high and stable defluoridation performance over a wide range of pH from 4 to 9. The superior uptake capacity and affinity for fluoride of LaLiAl-LDH@201 over LiAl-LDH@201 were driven by both the increased anion exchange capacity of the embedded LDHs and the specific La-F interaction evidenced via XPS and TEM-EDS characterisation. Fixed-bed column test confirmed that the working capacity of LaLiAl-LDH@201 for defluoridation of authentic fluoride-rich groundwater was nearly twice that of LiAl-LDH@201. The fluoride-loaded LaLiAl-LDH@201 could be conveniently regenerated in situ by using NaOH + NaCl binary solution, achieving desorption efficiency above 98%. Moreover, negligible capacity loss, La leaching, or structure alteration was observed after five adsorption-regeneration cycles, indicating the high stability of LaLiAl-LDH@201. Therefore, the novel millisphere nanocomposite LaLiAl-LDH@201 was promising for efficient defluoridation from water and wastewater.

Rational Design of Antifouling Polymeric Nanocomposite for Sustainable Fluoride Removal from NOM-Rich Water.

The presence of natural organic matter (NOM) exerts adverse effects on adsorptive removal of various pollutants including fluoride from water. Herein, we designed a novel nanocomposite adsorbent for preferable and sustainable defluoridation from NOM-rich water. The nanocomposite (HZO@HCA) is obtained by encapsulating hydrous zirconium oxide nanoparticles (HZO NPs) inside hyper-cross-linked polystyrene anion exchanger (HCA) binding tertiary amine groups. Another commercially available nanocomposite HZO@D201, with the host of a cross-linked polystyrene anion exchanger (D201) binding ammonium groups, was involved for comparison. HZO@HCA features with abundant micropores instead of meso-/macropores of HZO@D201, resulting in the inaccessible sites for NOM due to the size exclusion. Also, the tertiary amine groups of HCA favor an efficient desorption of the slightly loaded NOM from HZO@HCA. As expected, Sigma-Aldrich humic acid even at 20 mg of DOC/L did not exert any observable effect on fluoride sequestration by HZO@HCA, whereas a significant inhibition was observed for HZO@D201. Cyclic adsorption runs further verified the superior reusability of HZO@HCA for defluoridation from NOM-rich water. In addition, the HZO@HCA column could generate ∼80 bed volume (BV) effluent from a synthetic fluoride-containing groundwater to meet the drinking water standard (<1.5 mg F/L), whereas HCA and HZO@D201 columns could only generate <5 and ∼40 BV effluents, respectively. This study is believed to shed new light on how to rationally design antifouling nanocomposites for water remediation.

Enhanced selective adsorption of benzotriazole onto nanosized zeolitic imidazolate frameworks confined in polystyrene anion exchanger

A new nanocomposite adsorbent ZIF-67/D201, in which nanocrystalline ZIF-67 were immobilized inside the networking pores of a commercial polystyrene anion exchanger D201 by an alternate deposition method, with high capacity and enhanced selective affinity toward benzotriazole (BTA) was fabricated and characterized. ZIF-67/D201 demonstrated precise selective adsorption of BTA when benzimidazole (BMA), with very similar chemical structure to BTA, coexisted. After the uptake of BTA, ZIF-67/D201 could be regenerated for repeated use with slight capacity loss. According to kinetics data, two diffusion steps driven by electrostatic attraction were found prior to adsorption equilibrium: a fast diffusion of the contaminant into mesopores of D201 and then a relatively slow diffusion into micropores of ZIF-67. The underlying mechanism for the enhanced selective adsorption was revealed by spectral analysis and density functional theory (DFT) calculations. Three sorts of interactions (coordination, electrostatic attraction and π-π interaction) contributed to the fixing of contaminants. Among them, coordination was the predominant effect. For each sort of interaction, the binding energy of adsorbent-BTA was always larger than that of adsorbent-BMA, which was the intrinsic reason of the high selectivity in molecular level. The above results provided a strategy for precise separation of components with similar structures in water.

Self-crosslinking of comb-shaped polystyrene anion exchange membranes for alkaline fuel cell application

A series of crosslinked, comb-shaped polystyrene (PS) anion exchange membranes (AEMs) having C-16 alkyl side chain were synthesized by a Cu(I)-catalyzed “click chemistry” reaction, and subsequently azide-assisted self-crosslinking for alkaline fuel cell application. The as-obtained crosslinked AEMs showed lower water uptake, and thus good dimensional stability as a result of crosslinking. The chemical stabilities of the AEMs were evaluated under severe conditions, and minor degradation was observed by measuring IEC and ion conductivity changes after stability testing. The crosslinked membranes retained their high ion conductivity even in 10M NaOH at 80°C for 400h. Moreover, the PS-based AEMs shown higher hydroxide conductivity than that of the AEMs based on poly(2,6-dimethyl-phenylene oxide) (PPO) with similar architecture under the same testing condition probably due to the excellent compatibility between polystyrene backbone and alkyl side chain which may have helped to build a more efficient morphology for water uptake and thus the ion transport. These crosslinked cationic polymers were employed as membranes for alkaline fuel cells. The results indicated that the AEMs based on PPO having C-16 alkyl side chain had not initial performance, e.g. no open circuit voltage (OCV). In contrast, the initial fuel cell performance with the peak power density of 88mW/cm2 was observed for the alkaline fuel cell with xPS-65 membrane. It is assumed that the polystyrene polymer backbone may have helped to build a more efficient phase boundary between the catalyst layer and membrane probably resulted from the high water uptake though a more complete study would be needed to explain this phenomenon.

UV-crosslinking of polystyrene anion exchange membranes by azidated macromolecular crosslinker for alkaline fuel cells

Poly(2,6-dimethyl-phenyleneoxide)s (PPO)s with photo-crosslinkable azide groups were employed as macromolecular crosslinker for poly(vinylbenzyl chloride) (PVBC)-based anion exchange membranes (AEMs). The crosslinked AEMs were achieved by solution casting and UV- irradiation, subsequently quaternization with trimethylamine. Although the presence of azide groups in IR spectra in crosslinked AEMs suggested the incomplete reaction of azide groups using UV-irradiation, the gel fractions were more than 85% indicating the successful crosslinking between PVBC and PPO macromolecular crosslinker. The key properties of the crosslinked AEMs, such as mechanical property, ion exchange capacity, thermal stability, water uptake, ion conductivity, alkaline stability and initial H2/O2 fuel cell performance were investigated. Excellent mechanical properties were observed for all of the crosslinked AEMs. The as-obtained AEMs showed comparable λ-normalized hydroxide conductivity with previous reported crosslinked AEMs. The highest hydroxide conductivity of 14.8mS/cm at 20°C was achieved for the crosslinked AEMs with IEC value of 1.95meq./g in spite of its low water uptake (19.8wt%). Moreover, excellent alkaline stability was observed for crosslinked AEMs, 15% decrease in hydroxide conductivity after alkaline stability testing 1M NaOH at 80°C for 500h, while the conductivity of uncrosslinked membrane with similar IEC value decreased sharply with 58% of conductivity loss after only 120h. The improved alkaline stability of the crosslinked AEMs may be derived from its compact crosslinked architecture, protecting the cations from severe degradation. A peak power density of 11mW/cm2 was obtained at 16mA/cm2 when the crosslinked AEM was used as polymer electrolyte membrane in H2/O2 alkaline fuel cell at 60°C.

Two-step adsorption kinetics of malachite green on anionic polystyrene microspheres in aqueous solution probed by second harmonic generation.

Adsorption of organic cations of malachite green (MG) on an anionic microsphere surface was monitored in real time using a surface-specific second-harmonic generation (SHG) technique. This adsorption was found to consist of two processes of different timescales for all MG concentrations, which has not been considered in previous SHG experiments. The two-step adsorption can be well explained by our suggested model, which consists of an initial fast electrostatic alignment of weakly bound MG followed by slow non-electrostatic adsorption of MG on the surface of a microsphere. This study shows the importance of kinetics measurements in providing full understanding of adsorption of charged molecules on colloid surfaces.

Cadmium Removal from Contaminated Water Using Polyelectrolyte-Coated Industrial Waste Fly Ash.

Fly ash (FA) is a major industrial waste generated from power stations that add extra cost for proper disposal. Recent research efforts have consequently focused on developing ways to make use of FA in environmentally sound applications. This study, therefore, investigates the potential ability of raw fly ash (RFA) and polyelectrolyte-coated fly ash (PEFA) to remove cadmium (Cd) from polluted water. Using layer-by-layer approach, functionalized fly ash was coated with 20 layers from 0.03% (v/v) of cationic poly(diallyldimethylammonium chloride) (PDADMAC) and anionic polystyrene sulfonate (PSS) solutions. Both surface morphology and chemical composition of the adsorbent (PEFA) were characterized using Field-Emission Scanning Electron Microscope (FE-SEM), X-Ray Diffraction (XRD), Fourier-Transform Infrared (FTIR), and X-Ray Fluorescence (XRF) techniques. The effects of pH, adsorbent dosage, contact time, initial contaminant concentration, and mixing rate of the adsorption of Cd were also studied in batch mode experiments. Results of the study revealed that a 4.0 g/L dosage of PEFA removed around 99% of 2.0 mg/L of Cd in 15 min at 150 rpm compared to only 27% Cd removal achieved by RFA under the same conditions. Results also showed that adsorption by PEFA followed both Langmuir and Freundlich models with correlation coefficients of 98% and 99%, respectively.

Effective removal of glyphosate from water by resin-supported double valent nano-sized hydroxyl iron oxide

The double valent composite resin (DR) was prepared within nano-sized Fe(ii) and Fe(iii) hydroxyl oxide crosslinking polystyrene anion exchanger resin for efficient glyphosate removal from water.

Growth Kinetics in Layer-by-Layer Assemblies of Organic Nanoparticles and Polyelectrolytes.

The growth rates of layer-by-layer (LbL) assemblies of polyelectrolytes (PEs) with oppositely charged polystyrene (PS) nanoparticles (NPs) as a function of molecular weight (MW) of the PEs, ionic strength of the media, and NP size and charge are systematically investigated. To optimize LbL growth, the effects of suspension concentration, pH of the media, and deposition time on the growth rate of multilayers are assessed. Both linear and exponential growth behaviors are observed and, under optimal conditions, films of up to around 1 μm thick can readily be assembled after 10 or so bilayers have been deposited. For many of the cases studied, an intermediate MW of PE leads to the fastest film buildup, for both cationic poly(ethyleneimine) deposited alternately with anionic PS NPs and for anionic poly(acrylic acid) deposited alternately with cationic PS NPs. The existence of an optimal MW suggests that growth rate is determined by a balance of thermodynamic factors, including density of polymer bridges between particles, and kinetic factors, specifically the diffusivity of polymer in the film. The optimal MW, however, is very sensitive to the materials used. Moreover, depending on the MW of the PE, increasing salinity could increase or decrease the growth kinetics. Finally, the surface morphology of the films is characterized with AFM and SEM to reveal that the roughness increases less than linearly with film thickness.

Endocytosed nanoparticles hold endosomes and stimulate binucleated cells formation.

BackgroundNanotechnology developed rapidly in cellular diagnosis and treatment, the endocytic system was an important pathway for targeting cell. In the research of developing macrophages as drug carriers or important therapeutic targets, an interesting phenomenon, internalized nanoparticles induced to form binucleated macrophages, was found although the particles dose did not cause obvious cytotoxicity.ResultsUnder 25 μg/ml, internalized 30 nm polystyrene beads(30 nm Ps nanoparticles) induced the formation of binucleated macrophages when they entered into endosomes via the endocytic pathway. These internalized 30 nm Ps nanoparticles (25 μg/ml) and 30 nm Au-NPs (1.575 ng/ml) also induced markedly rise of binucleated cell rates in A549, HePG-2 and HCT116. This endosome, aggregated anionic polystyrene particles were dispersed and bound on inner membrane, was induced to form a large vesicle-like structure (LVLS). This phenomenon blocked transport of the particles from the endosome to lysosome and therefore restricted endosomal membrane trafficking through the transport vesicles. Early endosome antigen-1 and Ras-related protein-11 expressions were upregulated; however, the localized distributions of these pivotal proteins were altered. We hypothesized that these LVLS were held by the internalized and dispersed particles decreasing the amount of cell membrane available to support the completion of cytokinesis. In addition, altered distributions of pivotal proteins prevented transfer vesicles from fusion and hampered the separation of daughter cells.Conclusions30 nm Ps nanoparticles induced formation of LVLS, blocked the vesicle transport in endocytic system and the distributions of regular proteins required in cytokinesis which led to binucleated cells of macrophages. Markedly raised binucleated rate was also observed in human lung adenocarcinoma epithelial cell line(A549), human hepatoma cell line(HePG-2) and human colorectal cancer cell line(HCT116) treated by 30 nm Ps nanoparticles and Au-NPs.Electronic supplementary materialThe online version of this article (doi:10.1186/s12989-016-0173-1) contains supplementary material, which is available to authorized users.

Characterization of poly(methyl methacrylate)-graft-poly(styrene)s using various chromatographic techniques

Two graft copolymer samples of identical average composition were synthesized by grafting living polystyrene anions onto a broadly distributed PMMA backbone. Size exclusion chromatography (SEC) with only RI-detection, SEC with viscometry and light scattering detection, SEC with UV and RI dual detection, gradient chromatography and 2-dimensional chromatography were applied to compare the information that can be obtained by the different techniques. While only limited information was retrieved by conventional SEC or SEC with molar mass sensitive detection, SEC with UV and RI revealed different chemical heterogeneity of the samples. Using gradient chromatography and 2-dimensional chromatography it was possible to identify non-grafted side chains and unreacted parent PMMA besides the actual graft copolymer molecules. While in one sample a heavily grafted product was formed besides non-grafted PMMA, the second sample did not contain ungrafted PMMA but a graft product of lower grafting density. The different product distributions were explained by the different synthetic procedures.

Efficient defluoridation of water using reusable nanocrystalline layered double hydroxides impregnated polystyrene anion exchanger

Water decontamination from fluoride is still a challenging task of global concern. Recently, Al-based layered double hydroxides (LDHs) have been extensively studied for specific fluoride adsorption from water. Unfortunately, they cannot be readily applied in scaled-up application due to their ultrafine particles as well as the regeneration issues caused by their poor stability at alkaline pHs. Here, we developed a novel (LDH)-based hybrid adsorbent, i.e., LALDH-201, by impregnating nanocrystalline Li/Al LDHs (LADLH) inside a commercial polystyrene anion exchanger D201. TEM image and XRD spectra of the resultant nanocomposite confirmed that the LDHs particles were nanosized inside the pores of D201 of highly crystalline nature and well-ordered layer structure. After impregnation, the chemical and mechanical stability of LALDH were significantly improved against pH variation, facilitating its application at a wide pH range (3.5–12). Fluoride adsorption onto LALDH-201 was compared to D201 and activated alumina, evidencing the preferable removal fluoride of LALDH-201. Fluoride adsorption onto LALDH-201 followed pseudo-second-order model, with the maximum capacity (62.5 mg/g from the Sips model) much higher than the other two adsorbents. Fixed-bed adsorption run indicated the qualified treatable volume of the fluoride contaminated groundwater (4.1 mg/L initially) with LALDH-201 was about 11 times as much as with the anion exchanger D201 when the breakthrough point was set as 1.5 mg/L. The capacity of LALDH-201 could be effectively refreshed for continuous column operation without observable loss by using the mixed solution of 0.01 M NaOH + 1 M NaCl. The above results suggested that the hybrid adsorbent LALDH-201 is very promising for water defluoridation in scaled-up application.

Toward More Free-Floating Model Cell Membranes: Method Development and Application to Their Interaction with Nanoparticles.

Identifying the mechanisms of nanoparticle (NP) interactions with cell membranes is key to understanding potential NP cytotoxicity and applications as nanocarriers for targeted drug delivery. To elucidate these mechanisms of interaction, supported phospholipid bilayers (SPBs) are commonly used as models of cell membranes. However, SPBs are soft thin films, and, as such, their properties can be significantly affected by the underlying substrate. Free-floating cell membranes would be best modeled by weakly adhered SPBs; thus, we propose a method for tailoring the interfacial interaction of an electrically charged SPB-substrate system based on modulations in the solution chemistry. Using the dissipation signal of the quartz crystal microbalance with dissipation monitoring (QCM-D), we show that the method can be used to tailor SPB-substrate interactions without the loss of its structural integrity. To demonstrate the application of the method, SPBs are exposed to cationic and anionic polystyrene latex NPs. These studies reveal that the bilayer response to the modulations in the interfacial interaction with its underlying substrate can be used as a sensitive tool to probe the integrity of SPBs upon exposure to NPs. As expected, anionic NPs tend to impart no significant damage to the anionic bilayers, whereas cationic NPs can be detrimental to bilayer integrity. This is the first report of a QCM-D based method to probe bilayer integrity following exposure to NPs. Importantly, the degree of SPB interaction with its underlying substrate is shown to be a critical factor in the kinetics of bilayer disruption by cationic NPs, whereby weakly adhered bilayers are prone to significantly faster breakup. Since free-floating cell membranes are better represented by a weakly adhered SPB, the results of this work critically influence paradigms in experimental studies involving SPBs as models for cell membranes.

Hydroxide ion transfer in anion exchange membrane: A density functional theory study

A theoretical investigation of hydroxide ion transport mechanism in quaternary ammonium functionalized polystyrene (QAPS) anion exchange membrane (AEM) was studied by density functional theory (DFT). The results showed that there were two steps for OH− transferring through QAPS-AEM. The first step was the movement of OH− in water channel, which was induced by frequently forming and breaking of hydrogen bonds (H-bonds) between H2O and OH−. The second step was that OH− transferred across the quaternary ammonium (QA) groups by following the rotation about CC single bond, which was the rate-determining step for OH− transferring in QAPS-AEM. We presented that the ionic groups on the side chain of polymer with smaller space steric should provide higher ion conductivity due to their lower rotation energy barriers.

Enhanced Phosphate Removal by Nanosized Hydrated La(III) Oxide Confined in Cross-linked Polystyrene Networks.

A new nanocomposite adsorbent La-201 of extremely high capacity and specific affinity toward phosphate was fabricated and well characterized, where hydrated La(III) oxide (HLO) nanoclusters were immobilized inside the networking pores of the polystyrene anion exchanger D-201. La-201 exhibited enhanced phosphate adsorption in the presence of competing anions (chloride, sulfate, nitrate, bicarbonate, and silicate) at greater levels (up to molar ratio of 20), with working capacity 2-4 times higher than a commercial Fe(III) oxide-based nanocomposite HFO-201 in batch runs. Column adsorption runs by using La-201 could effectively treat ∼6500 bed volumes (BV) of a synthetic feeding solution before breakthrough occurred (from 2.5 mg P/L in influent to <0.5 mg P/L in effluent), approximately 11 times higher magnitude than that of HFO-201. The exhausted La-201 could be regenerated with NaOH-NaCl binary solution at 60 °C for repeated use without any significant capacity loss. The underlying mechanism for the specific sorption of phosphate by La-201 was revealed with the aid of STEM-EDS, XPS, XRD, and SSNMR analysis, and the formation of LaPO4·xH2O is verified to be the dominant pathway for selective phosphate adsorption by the immobilized nano-HLO. The results indicated that La-201 was very promising in highly efficient removal of phosphate from contaminated waters.

Implication of mesoporous 3-D graphene skeleton platform based on interconnected framework architecture in constructing electro-conductive flexible nanocomposites

Various polymer nanocomposites exhibiting elecro-conductivity along with flexibility were successfully fabricated by construction of the graphene-based three-dimensional (3-D) mesoporous skeleton platform derived from 3-D interconnected framework architecture constituted with two-dimensional (2-D) graphitic nanosheets, and the subsequent infiltration of polymer into pore volumes of the skeleton platform. The mesoporous 3-D skeleton platform of graphene has been easily constructed by the aggregation of graphene-coated polystyrene (PS) hybrid spheres prepared through ionic interacton between anionic graphene nanosheets and cationic PS nanospheres, and the subsequent thermal removal of polymer components, which made it possible to provide well-made pathways for electron transport as well as empty pores for the following infiltration of polymer matrix component. When a flexible polymer such as PVDF-HFP was chosen as a polymer matrix component entering into pore volumes of the graphene skeleton platform, the graphene/polymer nanocomposite tended to exhibit interesting behavior of electrical conductivity, which is comparable to that of neat graphene skeleton platform, and also maintained the initial value even under half-folding condition, evidencing excellent structural stability of the graphene skeleton. Furthermore, it was found that exchange of polymer matrix does not significantly alter the electrical conductivity of nanocomposite, confirming again the performance of 3-D graphene skeleton employing interconnected framework architecture as electron transport pathway. The ability to embed 3-D graphene skeleton into polymer matrix is a great opportunity to impart high electrical and mechanical properties to polymer composite formulation. Open image in new window

Reversing adhesion with light: a general method for functionalized bead release from cells.

Coated beads retain great importance in the study of cell adhesion and intracellular communication; we present a generally applicable method permitting spatiotemporal control of bead adhesion from cells. Herein we demonstrate in vitro release of a poly-d-lysine (PDL) layer from anionic polystyrene beads, allowing complete bead release from rat cortical neurons post-adhesion.

Phagocytosis-coupled flow cytometry for detection and size discrimination of anionic polystyrene particles

Flow cytometry was evaluated for its capacity to detect and distinguish a wide size range (20–2000nm) of fluorescent polystyrene particles (PSPs). Side scatter and fluorescence parameters could predict dispersed PSP sizes down to 200nm, but the forward scatter parameter was not discriminatory. Confocal microscopy of flow-sorted fractions confirmed that dispersed PSPs appeared as a single sharp peak on fluorescence histograms, whereas agglomerated PSPs were detected as smaller adjacent peaks. Particles as small as 200nm could also be detected by flow cytometry after they were first phagocytized by J774A.1 murine macrophages. Confocal microscopy demonstrated that these PSPs were internalized within the cytoplasm. MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] and calcein–AM (acetoxymethyl ester) assays showed that they were not cytotoxic. Internalized PSP size correlated to both cellular side scatter (R2=0.9821) and fluorescence intensity (R2=0.9993). Furthermore, PSPs of various sizes could be distinguished when J774A.1 cells were loaded with a single size of PSP and mixed with cells containing other sizes. However, spectra of cells loaded with a mixture of PSP sizes resembled those containing only the largest PSP. These data demonstrate the capacity and limitations of phagocytosis-coupled flow cytometry to distinguish between dispersed and agglomerated states and detect a wide size range of particles.

Nanoparticle–lipid bilayer interactions studied with lipid bilayer arrays

The widespread environmental presence and commercial use of nanoparticles have raised significant health concerns as a result of many in vitro and in vivo assays indicating toxicity of a wide range of nanoparticle species. Many of these assays have identified the ability of nanoparticles to damage cell membranes. These interactions can be studied in detail using artificial lipid bilayers, which can provide insight into the nature of the particle-membrane interaction through variation of membrane and solution properties not possible with cell-based assays. However, the scope of these studies can be limited because of the low throughput characteristic of lipid bilayer platforms. We have recently described an easy to use, parallel lipid bilayer platform which we have used to electrically investigate the activity of 60 nm diameter amine and carboxyl modified polystyrene nanoparticles (NH2-NP and COOH-NP) with over 1000 lipid bilayers while varying lipid composition, bilayer charge, ionic strength, pH, voltage, serum, particle concentration, and particle charge. Our results confirm recent studies finding activity of NH2-NP but not COOH-NP. Detailed analysis shows that NH2-NP formed pores 0.3-2.3 nm in radius, dependent on bilayer and solution composition. These interactions appear to be electrostatic, as they are regulated by NH2-NP surface charge, solution ionic strength, and bilayer charge. The ability to rapidly measure a large number of nanoparticle and membrane parameters indicates strong potential of this bilayer array platform for additional nanoparticle bilayer studies.