Interaction Of Silica Research Articles

Lysozyme is Sterically Trapped Within the Silica Cage in Bioinspired Silica-Lysozyme Composites: A Multi-Technique Understanding of Elusive Protein-Material Interactions.

Lysozyme is widely known to promote the formation of condensed silica networks from solutions containing silicic acid, in a reproducible and cost-effective way. However, little is known about the fate of the protein after the formation of the silica particles. Also, the relative arrangement of the different components in the resulting material is a matter of debate. In this study, we investigate the nature of the protein–silica interactions by means of solid-state nuclear magnetic resonance spectroscopy, small-angle X-ray scattering, and electron microscopy. We find that lysozyme and silica are in intimate contact and strongly interacting, but their interaction is neither covalent nor electrostatic: lysozyme is mostly trapped inside the silica by steric effects.

Heterogeneous Rate Constant for Amorphous Silica Nanoparticle Adsorption on Phospholipid Monolayers.

The interaction of amorphous silica nanoparticles with phospholipid monolayers and bilayers has received a great deal of interest in recent years and is of importance for assessing potential cellular toxicity of such species, whether natural or synthesized for the purpose of nanomedical drug delivery and other applications. This present communication studies the rate of silica nanoparticle adsorption on to phospholipid monolayers in order to extract a heterogeneous rate constant from the data. This rate constant relates to the initial rate of growth of an adsorbed layer of nanoparticles as SiO2 on a unit area of the monolayer surface from unit concentration in dispersion. Experiments were carried out using the system of dioleoyl phosphatidylcholine (DOPC) monolayers deposited on Pt/Hg electrodes in a flow cell. Additional studies were carried out on the interaction of soluble silica with these layers. Results show that the rate constant is effectively constant with respect to silica nanoparticle size. This is interpreted as indicating that the interaction of hydrated SiO2 molecular species with phospholipid polar groups is the molecular initiating event (MIE) defined as the initial interaction of the silica particle surface with the phospholipid layer surface promoting the adsorption of silica nanoparticles on DOPC. The conclusion is consistent with the observed significant interaction of soluble SiO2 with the DOPC layer and the established properties of the silica–water interface.

Effect of protein adsorption on the dissolution kinetics of silica nanoparticles

Nanoparticulate systems in the presence of proteins are highly relevant for various biomedical applications such as photo-thermal therapy and targeted drug delivery. These involve a complex interplay between the charge state of nanoparticles and protein, the resulting protein conformation, adsorption equilibrium and adsorption kinetics, as well as particle dissolution. SiO2 is a common constituent of bioactive glasses used in biomedical applications. In this context, the dissolution behavior of silica particles in the presence of a model protein, bovine serum albumin (BSA), at physiologically relevant pH conditions was studied. Sedimentation analysis using an analytical ultracentrifuge showed that BSA in the supernatant solution is not affected by the presence of silica nanoparticles. However, zeta potential measurements revealed that the presence of the protein alters the particles’ charge state. Adsorption and dissolution studies demonstrated that the presence of the protein significantly enhances the dissolution kinetics via interactions of positively charged amino acids in the protein with the negative silica surface and interaction of BSA with dissolved silicate species. Our study provides comprehensive insights into the complex interactions between proteins and oxide nanoparticles and establishes a reliable protocol paving the way for future investigations in more complex systems involving biological solutions as well as bioactive materials.

Silica nanoparticle-loaded thermoresponsive block copolymer vesicles: a new post-polymerization encapsulation strategy and thermally triggered release.

A thermoresponsive amphiphilic diblock copolymer that can form spheres, worms or vesicles in aqueous media at neutral pH by simply raising the dispersion temperature from 1 °C (spheres) to 25 °C (worms) to 50 °C (vesicles) is prepared via polymerization-induced self-assembly (PISA). Heating such an aqueous copolymer dispersion from 1 °C up to 50 °C in the presence of 19 nm glycerol-functionalized silica nanoparticles enables this remarkable ‘shape-shifting’ behavior to be exploited as a new post-polymerization encapsulation strategy. The silica-loaded vesicles formed at 50 °C are then crosslinked using a disulfide-based dihydrazide reagent. Such covalent stabilization enables the dispersion to be cooled to room temperature without loss of the vesicle morphology, thus aiding characterization and enabling the loading efficiency to be determined as a function of both copolymer and silica concentration. Small-angle X-ray scattering (SAXS) analysis indicated a mean vesicle membrane thickness of approximately 20 ± 2 nm for the linear vesicles and TEM studies confirmed encapsulation of the silica nanoparticles within these nano-objects. After removal of the non-encapsulated silica nanoparticles via multiple centrifugation–redispersion cycles, thermogravimetric analysis indicated that vesicle loading efficiencies of up to 86% can be achieved under optimized conditions. Thermally-triggered release of the silica nanoparticles is achieved by cleaving the disulfide bonds at 50 °C using tris(2-carboxyethyl)phosphine (TCEP), followed by cooling to 20 °C to induce vesicle dissociation. SAXS is also used to confirm the release of silica nanoparticles by monitoring the disappearance of the structure factor peak arising from silica–silica interactions.

Dry sliding behavior of copper based composite materials prepared using conventional compaction and sintering technique and spark plasma sintering

The study aimed to investigate the dry sliding properties of as received copper based composite materials, with varying silica and copper content, and produced through two different techniques: conventional compaction and sintering and spark plasma sintering (SPS). The SPS process induced pronounced densification and hardness of the materials and a better distribution of constituents when compared to conventionally sintered specimens. The SPS specimens observed the presence of a C layer of varying thickness on their surfaces, transferred from the graphite die used for their production. The thickness and adhesion of the C layer was influenced by the silica content in the specimens. Specimens containing low silica content showed a significant C layer on the pin surface. This C layer was not removed during dry sliding pin on disc testing, thus resulting in very low COF (coefficient of friction) and pin wear. Specimens containing high silica content led to the formation of a sparse C layer on their surfaces due to the low chemical interactions of silica with other atoms or compounds, leading to easy removal during tests and elevated COF magnitude. However, high silica content also led to low adhesion between the friction layer and the worn surfaces, resulting in instability and higher pin wear. The specimens containing moderate silica content were identified as the best composition due to their ability to easily shed the C layer during testing, maintain smooth, compact, and continuous friction layer without any detachment/adherence issues, and demonstrate permissible COF and pin wear in the mild range.

Super-Toughened Fumed-Silica-Reinforced Thiol-Epoxy Composites Containing Epoxide-Terminated Polydimethylsiloxanes.

In response to the demand for high-performance materials, epoxy thermosetting and its composites are widely used in various industries. However, their poor toughness, resulting from the high crosslinking density of the epoxy network, must be improved to expand their application to the manufacturing of flexible products. In this study, ductile epoxy thermosetting was produced using thiol compounds with functionalities of 2 and 3 as curing agents. The mechanical properties of the epoxy were further enhanced by incorporating fumed silica into it. To increase the filler dispersion, epoxide-terminated polydimethylsiloxane was synthesized and used as a composite component. Thanks to the polysiloxane–silica interaction, the nanosilica was uniformly dispersed in the epoxy composites, and their mechanical properties improved with increasing fumed silica content up to 5 phr (parts per hundred parts of epoxy resin). The toughness and impact strength of the composite containing 5 phr nanosilica were 5.17 (±0.13) MJ/m3 and 69.8 (±1.3) KJ/m2, respectively.

Hybrid Silica-Based Fillers in Nanocomposites: Influence of Isotropic/Isotropic and Isotropic/Anisotropic Fillers on Mechanical Properties of Styrene-Butadiene (SBR)-Based Rubber.

The improvement of mechanical properties of polymer-based nanocomposites is usually obtained through a strong polymer–silica interaction. Most often, precipitated silica nanoparticles are used as filler. In this work, we study the synergetic effect occurring between dual silica-based fillers in a styrene-butadiene rubber (SBR)/polybutadiene (PBD) rubber matrix. Precipitated Highly Dispersed Silica (HDS) nanoparticles (10 nm) have been associated with spherical Stöber silica nanoparticles (250 nm) and anisotropic nano-Sepiolite. By imaging filler at nano scale through Scanning Transmission Electron Microscopy, we have shown that anisotropic fillers align only in presence of a critical amount of HDS. The dynamic mechanical analysis of rubber compounds confirms that this alignment leads to a stiffer nanocomposite when compared to Sepiolite alone. On the contrary, spherical 250 nm nanoparticles inhibit percolation network and reduce the nanocomposite stiffness.

Effect of magnetic field on calcium - silica fouling and interactions in brackish water distribution systems

Fouling growth in brackish water distribution systems (BWDS), especially calcium-silica fouling, is inevitable issue in brackish water desalination, chemical and agricultural industry, eventually threaten the cleaner production process and environment. Magnetic Field (MF) has been a greener and effective technology to control calcium carbonate fouling. However, the effects of MF on composite calcium-silica fouling are still elusive. Therefore, this paper assessed the effect of MF on calcium and silica fouling. We found that MF not only significantly reduce the calcium carbonate fouling, but also obviously decreased the silica fouling. The MF reduced the calcite fouling reached 38.2%–64.3% by changing water quality parameters to trigger the transformation rate of CaCO3 crystal from compact calcite to looser aragonite, as well as increase the unit-cell parameters and chemical bond lengths of calcite and aragonite. The MF also decreased the content of silica fouling (silica and silicate) reached 22.4–46.3% by reducing the concentration of soluble silica and accelerating the flocculation settlement to form large size solid particles in BW. Furthermore, MF broke the synergistic interactions among calcium and silica fouling. In addition, the anti-fouling ability of permanent MF was higher by 12.3–35.1% than electric MF. Overall, these findings demonstrate that MF is an effective and chemical-free technology to control calcium-silica fouling in BWDS, and provide a new perspective for sustainable application of brackish water.

Discovering indium as hydrogen production booster for a Cu/SiO2 catalyst in steam reforming of methanol

We report on the use of In as an effective H2 production promoter in a Cu/SiO2 catalyst for the steam reforming of methanol. To date, In promotion has been limited to noble metals because of its tendency to “bury” other metals thus compromising the catalytic activity. Here, we prepared a silica-supported Cu-In catalyst via a urea-assisted co-precipitation method that showed a higher H2 productivity compared to the monometallic catalyst and a remarkable H2/CO2 molar ratio of almost 3 at 220 °C. Through XPS, XRPD and HRTEM-EDX along with H2- and CO-TPR, H2O-TPD, and N2O titrations, supported by computational modeling, we attributed such superior performances to an easier H2O activation due to improved electronic properties of the Cu phase, that is, its lower oxidation state via electron density transfer from the InOx buffer phase as a 1D “necklace” structures crucially mediating the interaction of small Cu nanoparticles (2.6 nm) and silica.

Hydrogen pre–reduction determined Co–silica interaction and performance of cobalt catalysts for propane dehydrogenation

[email protected]–41 catalysts with and without hydrogen pre–reduction treatments are prepared for catalyzing non–oxidative propane dehydrogenation (PDH) to propylene. Multi–stage migration of framework Co2+ into extra–framework Co0 species can be achieved by the pre–reduction. The location and chemical states of Co species in catalysts are related to the pre–reduction temperature and time duration. The catalysts reduced at 650–700 °C are consisting of both framework Co2+ ions and small–size Co0 nanoclusters confined in the MCM–41 channels, displaying 2–3 times higher reaction rates in the selective PDH reactions in comparison with the unreduced catalyst. A higher pre–reduction temperature of 750–800 °C causes the formation of large Co particles that are responsible for significantly declined reaction rates and propylene selectivity as well as severe coke deposition. Hydrogen pre–reduction tunes the interaction between Co species and silica support, determining the performances of propane activation, propylene desorption and coke formation for the Co–catalyzed PDH reactions.

Effective Enrichment Strategy Using Boronic Acid-Functionalized Mesoporous Graphene-Silica Composites for Intact N- and O-Linked Glycopeptide Analysis in Human Serum.

The heterogeneity and low abundance of protein glycosylation present challenging barriers to the analysis of intact glycopeptides, which is key to comprehensively understanding the role of glycosylation in an organism. Efficient and specific enrichment of intact glycopeptides could help greatly with this problem. Here, we propose a new enrichment strategy using a boronic acid (BA)-functionalized mesoporous graphene-silica composite (denoted as GO@mSiO2-GLYMO-APB) for isolating intact glycopeptides from complex biological samples. The merits of this composite, including high surface area and synergistic effect from size exclusion functionality of mesoporous material, hydrophilic interaction of silica, and the reversible covalent binding with BA, enable the effective and specific enrichment of both intact N- and O-glycopeptides. The results from the enrichment performance of the strategy evaluated by standard glycoproteins and the application to global N- and O-glycosylation analyses in human serum indicate the robustness and potential of the strategy for intact glycopeptide analysis.

Surface tension and wettability analysis during the interaction of alkali-nano silica and its effect on acidic crude oil

Surface tension and wettability analysis during the interaction of alkali-nano silica and its effect on acidic crude oil

Influence of Treated Distillate Aromatic Extract (TDAE) Content and Addition Time on Rubber-Filler Interactions in Silica Filled SBR/BR Blends.

High compatibility and good rubber–filler interactions are required in order to obtain high quality products. Rubber–filler and filler–filler interactions can be influenced by various material factors, such as the presence of processing aids. Although different processing aids, especially the plasticizers, and their effects on compatibility have been investigated in the literature, their influence on rubber–filler interactions in highly active filler reinforced mixtures is not explicit and has not been investigated in depth. For this purpose, the influence of treated distillate aromatic extract (TDAE) oil content and its addition time on interactions between silica and rubber chains were investigated in this study. Rubber–filler and filler–filler interactions of uncured and cured silica-filled SBR/BR blends were characterized by using rubber layer L concept and dynamic mechanical analysis, whereas mechanical properties were studied by tensile test and Shore A hardness. Five parts per hundred rubber (phr) TDAE addition at 0, 1.5, and 3 min of mixing were characterized to investigate the influence of TDAE addition time on rubber–filler interactions. It was observed that addition time of TDAE can influence the development of bounded rubber structure and the interfacial interactions, especially at short time of mixing, less than 5 min. Oil addition with silica at 1.5 min of mixing resulted in fast rubber layer development and a small reduction in storage shear modulus of uncured blends. The influence of oil content on rubber–filler and filler–filler interactions were investigated for the binary blends without oil, with 5 and 20 phr TDAE content. The addition of 5 phr oil resulted in a slight increase in rubber layer and 0.05 MPa reduction in Payne effect of uncured blends. The storage tensile modulus of vulcanizates at small strains decreased from 13.97 to 8.28 MPa after oil addition. Twenty parts per hundred rubber (phr) oil addition to binary blends caused rubber layer L to decrease from 0.45 to 0.42. The storage tensile modulus of the vulcanizates and its reduction with higher amplitudes were incontrovertibly high among the vulcanizates with lower oil content, which were 13.57 and 4.49 MPa, respectively. When any consequential change in mechanical properties of styrene–butadiene rubber (SBR)/butadiene rubber (BR) blends could not be observed at different TDAE addition time, increasing amount of oil in blends enhanced elongation at break, and decreased Shore A hardness and tensile strength.

Study on Ceria–Silica Interaction in Various Ce3+ Concentration for Effective Post Chemical Mechanical Planarization (CMP) Cleaning

Shallow trench isolation (STI) is a technology that isolates transistors by constructing trenches and filling them with silicon dioxide. The excess silica should be removed by a subsequent step, chemical mechanical planarization (CMP) process, without any damage to active area. To prevent the damage during polishing, the silicon nitride is used for a stopping layer.1 Therefore, in the CMP process in STI, oxide-to-nitride polishing selectivity is needed. Since ceria nanoparticles (NPs) has high removal rate on silicon oxide but low removal rate on silicon nitride, they are generally utilized for CMP in STI.2 Additionally, Ce3+ concentration on the ceria NPs is considerably related to the oxide-to-nitride selectivity. It was reported that as the Ce3+ concentration on ceria NPs increased, its oxide-to-nitride selectivity was improved.3 However, after CMP process, there exists large amount of contaminants on the substrates which is mainly originated from the abrasives and organic additives in CMP slurry. Especially, on the surface of silicon oxide, the residual ceria NPs caused problems in post-CMP cleaning. Since they have chemical interaction with silicon oxide as reported, they are not easily removed from the surface. As the demands for high-end semiconductor devices with enhanced performance soar, the contaminants should be successfully removed.4-6 Therefore, in-depth research on ceria-silica interaction for effective post-CMP cleaning receives large attention.We directly investigated the ceria-silica interaction using atomic force microscope (AFM) and quartz crystal microbalance (QCM). Using AFM, the adhesion energy between silicon oxide and ceria NPs was quantitatively measured with respect to Ce3+ concentration on the ceria NPs as shown in Figure 1. We changed the surface Ce3+ concentration on the ceria NPs using hydrogen peroxide and ultrasonication, which was classified as Ceria1 to Ceria4.7 Moreover, the adsorption behavior of ceria NPs on the surface of silicon oxide was observed by QCM depending on the surface Ce3+ concentration. From the results of adsorption rate, the activation energy for the ceria-silica adsorption was studied depending on the Ce3+ concentration on the ceria NPs, which is exhibited in Figure 2.Figure CaptionsFigure 1. Adhesion energy between ceria and silica depending on surface Ce3+ concentration.Figure 2. Plot of the natural logarithm of adsorption rate versus the reciprocal of temperature at different surface Ce3+ concentrations of ceria NPs.References M. C. Kang, J. J. Kim and D.-K. Moon, Jpn. J. Appl. Phys., 44, 5949 (2005).R. Srinivasan, P. V. R. Dandu and S. V. Babu, ECS J. Solid State Sci. Technol., 4, P5029 (2015).K. Kim, D. K. Yi and U. Paik, ECS J. Solid State Sci. Technol., 6, P681 (2017).H. S. Philip Wong, Solid-State Electron., 49, 755 (2005).M. Tsujimura, ECS J. Solid State Sci. Technol., 8, P3098 (2019).C. K. Ranaweera, N. K. Baradanahalli, R. Popuri, J. Seo and S. V. Babu, ECS J. Solid State Sci. Technol., 8, P3001 (2018).J. F. Changjian Ma, Jiaxiang Chen, Yaoyao Wen, Paul O Fasan, Hua Zhang, Nuowei Zhang,* Jinbao Zheng, and Bing-Hui Chen, Ind. Eng. Chem. Res., 56, 9090 (2017). Figure 1

Hybrid vesicles of pillar[5]arene/silica: Host-guest complexation and application in pH-triggered release

Integrating silica with organic nanoparticles can generate unique properties. Here pillar[5]arene/silica hybrid vesicles were constructed based on the amphiphilic and rigid properties of pillararenes, as well as the catalytic hydrolysis of tetraethoxysilane. Such vesicles exhibited the high strength of silica and unique molecular recognition of pillararenes, both of which could tune the pH-triggered release behavior. Furthermore, a rhodamine B derivative with hexyl group (RhB-C6) was synthesized, which can form a complex with the pillar[5]arene. Based on the host-guest interaction and high strength of silica, the hybrid vesicles could load more RhB-C6 and the rhodamine B was released more slowly compared with the organic vesicles.

Hofmeister effects in the gelling of silica nanoparticles in mixed salt solutions

Understanding the nature of specific interaction of ions with the charged silica nanoparticles is vital not only to produce gels for applications such as grouting but also for determining their long term stability. Interaction of silica nanoparticles in single salt solutions has been thoroughly investigated but in mixed salt solutions is rarely investigated. In this work we have investigated the gelling of silica nanoparticles in the mixtures of monovalent ions as well as in the mixtures of divalent and monovalent ions. To gain an understanding of the interaction of ions with the charged silica surface at molecular level we have performed molecular dynamics (MD) simulations. Our overall goal was to find out if in salt mixtures ions silica interactions follow the Hofmeister series or not and how ion specific interactions may change when chaotropic ions are successively replaced by kosmotropic or vice versa. The gelling results show that generally monvalent ions in salt mixtures follow the Hofmeister series, e.g., the gel times in the mixtures of lithium and sodium chlorides are much longer than in the mixtures of lithium and potassium chlorides. On the other hand, gel times in the salt mixtures containing divalent ions do not follow the expected Hofmeister series e.g. mixtures of magnesium and sodium chlorides show shorter gel times than that of calcium and sodium chlorides. However, pH dependent gelling revealed that at pH values less than 9 gelling in these mixtures follow the normal Hofmeister series i.e., longer gelling time in magnesium and sodium chlorides than in calcium and sodium chlorides. This reversal of Hofmeister series for divalent and monovalent salt mixtures at pH > 9 and normal Hofmeister series at pH < 9 is reported for the first time in literature. Such a revesal at pH> 9 is explained due to enhanced surface charge, ordring of surface water layer which leads to enhanced ion specificity of strongly hydrated ions such as Mg2+. Moreover, in mixtures having the same divalent salt but different monovalent salts such as magnesium chlorides mixtures with lithium, sodium and potassium chlorides a normal Hofmeister series prevails. MD simulations results revealed that Mg2+ ions retain their strong hydration shell while interacting with the oppositely charged silica surface which means that the shorter gelling times obtained in magnesium salts mixtures are not due to inner sphere complexation of magnesium with the silica surface. Instead magnesium interacts with the silica surface through its hydrating water molecules.

Diagenetic alteration, pore-throat network, and reservoir quality of tight gas sandstone reservoirs: A case study of the upper Paleozoic sequence in the northern Tianhuan depression in the Ordos Basin, China

The Sulige gas field in the Ordos Basin is the largest gas field in China. The studied area, the northern Tianhuan depression, is located west of the gas field and is considered as a potential gas-producing area. The complex diagenetic alteration history and its effects on the pore-throat network and reservoir quality of the tight gas sandstones are explained. The upper Paleozoic first member of the Shanxi Formation and eighth member of the Shihezi Formation tight gas reservoir rocks are composed of coarse- to medium-grained sandstones and are dominated by sublitharenites. The most important diagenetic factor for porosity reduction was compaction, followed by cementation. Diagenetic mineral phases include quartz overgrowth, calcite cement and replacement, and kaolinite cement and replacement, with minor heulandite and chlorite. Pressure dissolution of quartz grains and quartzite fragments is the main source of silica for the early and late quartz overgrowth cementation (formed mainly from 120°C to 140°C). The hydrolysis and alteration of volcanic material and mica flakes released some silicon, calcium, and aluminum ions. Calcium and carbon in calcite cements could be derived from surrounding mudstones. Calcite replaced the quartz overgrowths. The formation of kaolinite, as cement and replacements, was controlled by the interactions of silica, aluminum, pH, and temperature (140°C). Because of deformation of detrital components (mica flakes and ductile rock fragments) and diagenetic replacement, clear negative correlations between reservoir quality and contents of the diagenetic minerals are lacking. A complex and isolated pore-throat network was created by strong diagenetic transformation. Based on analysis of thin sections, three-dimensional x-ray micro–computed tomography, and constant-rate mercury injection data, the samples with relatively good reservoir quality (porosity >10% and permeability >0.5 md) are characterized by dissolution pores and primary intergranular pores and commonly contain more and larger pore throats both in volume (counts >1800 and size >0.02 per unit volume) and diameter (>1.20 μm) than the samples with poor reservoir quality. The intercrystalline pores of kaolinite are very widespread and considered favorable for oil and gas accumulation because some asphalt was found within these pores. This study may be used, by analogy, to better understand diagenetic factors controlling the formation of tight gas sandstone reservoirs and predict the development of pore-throat systems.

In Ukrainian

Nowadays, it is relevant to study the processes that occur at the boundary of biomolecule (cell)-nanoparticle phase distribution. There is a growing interest in studying the interaction of ultrafine silica (UFC) with saccharides, in particular glucose and fructose, as well as with N-acetylneuraminic acid (NANA) (which is а part of the body’s cell membrane), for further creation of nanocomposites with biomolecules to use in biological systems. Using the density functional theory method (DFT) within the polarization continuum model (PCM), the interaction peculiarities of monosaccharides with silica surface were examined and the influence of the NANA molecule on this process was determined. The results of the analysis of quantum chemical calculations indicate that glucose and fructose can be used as modifiers for NANA adsorption. The molecules of these carbohydrates are related to silica surface and form a complex with N-acetylneuraminic acid. It is found that hydrogen bonds between hydroxyl groups of carbohydrates and silanol groups of the UFC surface play a major part in the formation of intermolecular complexes. The calculations show that the adsorption of monosaccharides on silica surface is possible considering their location, and it also depends on how to carry out the adsorption. That is, whether the adsorption of saccharides and then of NANA, or the adsorption from monosaccharides-NANA solution on silica surface is sequential.

Surface Forces between Nanomagnetite and Silica in Aqueous Ca2+ Solutions Studied with AFM Colloidal Probe Method

Dispersion and aggregation of nanomagnetite (Fe3O4) and silica (SiO2) particles are of high importance in various applications, such as biomedicine, nanoelectronics, drug delivery, flotation, and pelletization of iron ore. In directly probing nanomagnetite–silica interaction, atomic force microscopy (AFM) using the colloidal probe technique has proven to be a suitable tool. In this work, the interaction between nanomagnetite and silica particles was measured with AFM in aqueous Ca2+ solution at different pH levels. This study showed that the qualitative changes of the interaction forces with pH and Ca2+ concentrations were consistent with the results from zeta-potential measurements. The repulsion between nanomagnetite and silica was observed at alkaline pH and 1 mM Ca2+ concentration, but no repulsive forces were observed at 3 mM Ca2+ concentration. The interaction forces on approach were due to van der Waals and electrical double-layer forces. The good fitting of experimental data to the DLVO model and simulations supported this conclusion. However, contributions from non-DLVO forces should also be considered. It was shown that an increase of Ca2+ concentration from 1 to 3.3 mM led to a less pronounced decrease of adhesion force with increasing pH. A comparison of measured and calculated adhesion forces with a few contact mechanics models demonstrated an important impact of nanomagnetite layer nanoroughness.

Chitosan/silica composite membrane: Performance on water permeability and rejection of lead(II) ion from aqueous solution

Heavy metal such as lead can be classified as non-biodegradable inorganic pollutants which can contaminate the soils, ground water, sediments and surface water. It cannot be broken down or decomposed by living organism and can continue to exist over a prolonged period, generating harmful effects to the living things. Thus, lead removal is necessary in order to reduce the amount of heavy metals contaminated in water. The purpose of this study was to fabricate chitosan/silica based composite membrane for removal of Pb(II) metal ions from aqueous solution by membrane filtration technique. The composite membranes were characterized in terms of morphological studies and functional group analysis by using Scanning Electron Microscopy (SEM) and Fourier Transform Infrared-Attenuated Total Reflectance (FTIR-ATR) analysis, respectively. The membrane permeation performance, in terms of water permeability and rejection of Pb(II) ions from aqueous solution, was conducted by using membrane permeation system. SEM images illustrated that the presence of macrovoids on the cross-section of the chitosan/silica composite membrane has improved the morphology of pure chitosan membrane and assisted in the rejection of Pb(II) ions. Meanwhile, FTIR-ATR spectra showed the presence of new adsorption peaks, contributed by silica interaction with hydroxyl group of chitosan. The addition of silica to chitosan membrane has significantly enhanced the pure water permeability from 37.36 L/m2h to 42.43 L/m2h. Furthermore, the rejection of Pb(II) metal ions by chitosan/silica composite membrane was slightly higher compared to pure chitosan membrane with the removal efficiency of 13.78% at 0.5 bar applied pressure. These findings indicates the potential use of silica to improve chitosan membrane properties and reduce heavy metal pollution in water.