Low-Gradient Magnetophoresis of Nanospheres and Nanorods through a Single Layer of Paper.

The possible magnetophoretic migration of iron oxide nanoparticles through the cellulosic matrix within a single layer of paper is challenging with its underlying mechanism remained unclear. Even with the recent advancements of theoretical understanding on magnetophoresis, mainly driven by cooperative and hydrodynamics phenomena, the contributions of these two mechanisms on possible penetration of magnetic nanoparticles through cellulosic matrix of paper have yet been proven. Here, by using iron oxide nanoparticles (IONPs), both nanospheres and nanorods, we have investigated the migration kinetics of these nanoparticles through grade 4 Whatman filter paper with a particle retention of 20-25 µm. By performing droplet tracking experiments, the real-time stained area growth of the particle droplet on the filter paper, under the influences of a grade N40 NdFeB magnet, were recorded. Our results show that the spatial and temporal expansion of the IONP stain is biased toward the magnet and such an effect is dependent on (i) particle concentration and (ii) particle shape. The kinetics data were first analyzed by treating it as a radial wicking fluid, and later the IONP distribution within the cellulosic matrix was investigated by optical microscopy. The macroscopic flow front velocities of the stained area ranged from 259 µm/s to 16 040 µm/s. Moreover, the microscopic magnetophoretic velocity of nanorod cluster was also successfully measured as ∼214 µm/s. Findings in this work have indirectly revealed the strong influence of cooperative magnetophoresis and the engineering feasibility of paper-based magnetophoretic technology by taking advantage of magnetoshape anisotropy effect of the particles.

Poly(vinyl alcohol)/Premna Oblongifolia Merr. Extract/Glutaraldehyde/Carbon Nanotube (VOGC)-Based Composite Hydrogel: A Potential Candidate for Controlled-Release Materials.

A hydrogel based on poly(vinyl alcohol) (V), Premna Oblongifolia Merr. extract (O), glutaraldehyde (G), and carbon nanotubes (C) has been synthesized in search of candidates to develop controlled-release fertilizers (CRF). Referring to previous studies, O and C can be considered as two materials that have potential as modifiers in synthesizing CRF. This work is comprised of hydrogel synthesis, their characterisation, including measuring swelling ratio (SR) and water retention (WR) of VOGm , VOGe , VOGm C3 , VOGm C5 , VOGm C7 , VOGm C7 -KCl, and release behaviour of KCl from VOGm C7 -KCl. We found that C interacts physically with VOG, increased the surface roughness of VOGm , and reduced the VOGm crystallite size. The addition of KCl into VOGm C7 reduced the pore size and increased the structural density of VOGm C7 . The thickness and the C content of VOG affected its SR and WR. The addition of KCl into VOGm C7 reduced its SR, but did not significantly affect its WR.

Selective non-enzymatic uric acid sensing in the presence of dopamine: electropolymerized poly-pyrrole modified with a reduced graphene oxide/PEDOT:PSS composite.

A highly selective electrochemical sensor based on a molecularly imprinted polymer (MIP) to be developed for uric acid detection in the presence of dopamine as an interference molecule was demonstrated in this study. This non-enzymatic uric acid sensor was developed by electropolymerizing poly-pyrrole onto a composite of electrochemically reduced graphene oxide (ErGO) and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) on a glassy carbon electrode (GCE) to give MIP/ErGO/PEDOT:PSS electrodes. The structural properties, surface morphology, and electrochemical interface of this fabricated uric acid sensor was then characterized using infrared spectroscopy, scanning electron microscopy, atomic force microscopy, and electrochemical impedance spectroscopy. This fabricated non-enzymatic electrochemical sensor (MIP/ErGO/PEDOT:PSS modified GCE) also showed excellent analytical performance at the optimum ratio of monomer/template concentration and optimized electropolymerization conditions, for example in the low concentration range of 0.1-100 µM with a detection limit of 0.05 µM towards uric acid detection in the presence of dopamine. Furthermore, this fabricated uric acid sensor also exhibited good reproducibility and stability for uric acid measurements in the presence of dopamine for 5 consecutive days. In addition, this sensor demonstrates highly selective detection of uric acid in the presence of several interfering species such as dopamine, urea, glucose, magnesium ions, and ascorbic acid. This fabricated uric acid sensor ultimately showed satisfactory uric acid measurement in samples of human urine and is expected to be used in early-stage disease diagnosis.

Promotional effect of Ca doping on Bi2Fe4O9 as peroxymonosulfate activator for gatifloxacin removal.

A series of Ca-doped bismuth ferrite was prepared at various %w/w of Ca via a facile hydrothermal method to obtain Bi2XCa2(1-X)Fe4O9 (denoted as BFOCa-X, where X = 1, 0.95, 0.90, 0.80, 0.50). The BFOCa-X catalysts were characterized, and the results showed that they consist of pure phase BFO with nanosheet-like morphology. The as-prepared BFOCa-X catalysts were used as peroxymonosulfate (PMS) activator for gatifloxacin (GAT) removal. It was found that the catalytic activity decreased in the following order: BFOCa-0.8 (90.2% GAT removal efficiency in 45 min, kapp = 0.084 min-1)>BFOCa-0.95 > BFOCa-0.9 > BFOCa-0.5 > BFO indicating that BFOCa-0.8 has the optimized active sites for catalysis. The Ca dopant contributed to the increased oxygen vacancies and surface hydroxyl groups, promoting the catalytic PMS activation process. The kapp value increased gradually with increasing catalyst loading and PMS dosage while pH 9 presented the highest GAT removal rate. The GAT degradation rate was inhibited by PO43-, humic acid and NH4+ but promoted in the presence of Cl-, NO3- and HCO3-. It was also found that the GAT can undergo several degradation pathways in the catalytic PMS system, which eventually mineralized into innocuous compounds. The dominant reactive oxygen species (ROS) were identified using chemical scavengers, revealing that SO4•-, 1O2 and •OH contributed significantly to GAT degradation. Based on the XPS study, PMS was activated by the Fe2+/Fe3+ redox cycling and oxygen vacancies to produce SO4•-/•OH and 1O2, respectively. Overall, the BFOCa-0.8 also showed excellent reusability up to at least 4 cycles with low Bi and Fe leaching (<7 and 62 µg L-1, respectively), indicating that it has promising potential for application as PMS activator for antibiotics removal.

Effects of Benzalkonium Chloride Contents on Structures, Properties, and Ultrafiltration Performances of Chitosan-Based Nanocomposite Membranes.

The effects of benzalkonium chloride (BKC) contents on the structure, properties, and ultrafiltration performance of chitosan-based nanocomposite membranes containing poly(ethylene glycol) and multi-walled carbon nanotube (chitosan/BKC/PEG/CNT) were examined. The membranes were prepared by a mixing solution method and phase inversion before being characterized with microscopic techniques, tensile tests, thermogravimetric analysis, water contact angle, and porosity measurements. The performance of the nanocomposite membranes in regard to permeability (flux) and permselectivity (rejection) was examined. The results show that the incorporation of BKC produced nanocomposite membranes with smaller pore structures and improved physico-chemical properties, such as an increase in porosity and surface roughness (Ra = 45.15 to 145.35 nm and Rq = 53.69 to 167.44 nm), an enhancement in the elongation at break from 45 to 109%, and an enhancement in the mechanical strength from 31.2 to 45.8 MPa. In contrast, a decrease in the membrane hydrophilicity (water contact angle increased from 56.3 to 82.8°) and a decrease in the average substructure pore size from 32.64 to 10.08 nm were observed. The membrane rejection performances toward Bovine Serum Albumin (BSA) increased with the BKC composition in both dead-end and cross-flow filtration processes. The chitosan/BKC/PEG/CNT nanocomposite membranes have great potential in wastewater treatments for minimizing biofouling without reducing the water purification performance.

Offretite Zeolite Single Crystals Synthesized by Amphiphile-Templating Approach.

Offretite zeolite synthesis in the presence of cetyltrimethylammonium bromide (CTABr) is reported. The offretite crystals were synthesized with a high crystallinity and hexagonal prismatic shape after only 72 h of hydrothermal treatment at 180 °C. The CTABr has dual-functions during the crystallization of offretite, viz. as structure-directing agent and as mesoporogen. The resulting offretite crystals, with a Si/Al ratio of 4.1, possess more acid sites than the conventional offretite due to their high crystallinity and hierarchical structure. The synthesized offretite is also more reactive than its conventional counterpart in the acylation of 2-methylfuran for biofuel production under non-microwave instant heating condition, giving 83.5% conversion with 100% selectivity to the desired product 2-acetyl-5-methylfuran. Hence, this amphiphile synthesis approach offers another cost-effective and alternative route for crystallizing zeolite materials that require expensive organic templates.

Toughened chitosan-based composite membranes with antibiofouling and antibacterial properties via incorporation of benzalkonium chloride.

Biofouling due to biofilm formation is a major problem in ultrafiltration membrane applications. In this work, a potential approach to solve this issue has been developed by functionalization of chitosan-based membranes with benzalkonium chloride (BKC). The chitosan composite membranes consisting of poly(ethylene glycol) (PEG), multiwalled carbon nanotubes (MWCNT), and BKC were synthesized by mixing the membrane precursors and the antibacterial solution, and casting via an inversed phase technique. The effects of the BKC content on the morphology and performance of the membranes are investigated by varying the BKC feed compositions. The composite membranes demonstrate better antibacterial efficacy against Staphylococcus aureus than Escherichia coli. The permeability and selectivity performances of the composites as filter membranes are examined by employing a dead-end filtration system. Interestingly, enhanced toughness of the membranes is observed as a function of the BKC content. Mechanisms of the structural formation are investigated. The results from SEM, XRD, and FTIR spectroscopy revealed that MWCNT/BKC are located as nanoclusters with π-π stacking interactions, and are covered by PEG chains. The shape of the dispersed domains is spherical at low BKC contents, but becomes elongated at high BKC contents. These act as soft domains with an anisotropic shape with toughening of the brittle chitosan matrix, leading to enhanced durability of the membranes, especially in ultrafiltration applications. The composite membranes also demonstrate improved rejection in dead-end ultrafiltration systems due to high porosity, high hydrophilicity, and the positive charges of the membrane surface.

Decoration of an inorganic layer with nickel (hydr)oxide via green plasma electrolysis.

In this study, we describe the green plasma electrolysis of a magnesium alloy in alkaline electrolyte to produce a hybrid inorganic layer with nickel (hydr)oxide incorporated in a matrix of magnesium oxide, and investigate the electrochemical and optical properties of this material. The addition of Ni(NO3)2·6H2O to the electrolyte reduced the size of the micro-defects found in the inorganic layer after plasma electrolysis by inducing soft plasma discharges. As a result, through cyclic voltammetry and polarization tests, the corrosion stability of the sample containing nickel (hydr)oxide was significantly enhanced. Measurement of the optical properties reveals that the material possesses excellent energy efficiency as indicated by a high solar absorptivity of ∼0.92 and a low infrared emissivity of ∼0.13 which are presumably due to the inherent dark-brown colour of nickel (hydr)oxide. We expect that these results will have implications in the development of functional materials with excellent optical and corrosion properties by considering green processing utilizing alkaline electrolyte.

Aqueous nanosilica dispersants for carbon nanotube.

Nanosilicas can disperse single-wall carbon nanotube (SWCNT) in aqueous solution efficiently; SWCNTs are stably dispersed in aqueous media for more than 6 months. The SWCNT dispersing solution with nanosilica can produce highly conductive transparent films which satisfy the requirements for application to touch panels. Even multiwall carbon nanotube can be dispersed easily in aqueous solution. The highly stable dispersion of SWCNTs in the presence of nanosilica is associated with charge transfer interaction which generates effective charges on the SWCNT particles, giving rise to electrostatic repulsion between the SWCNTs in the aqueous solution. Adhesion of charged nanosilicas on SWCNTs in the aqueous solution and a marked depression of the S11 peak of optical absorption spectrum of the SWCNT with nanosilicas suggest charge transfer interaction of nanosilicas with SWCNT. Thus-formed isolated SWCNTs are fixed on the flexible three-dimensional silica jelly structure in the aqueous solution, leading to the uniform and stable dispersion of SWCNTs.

Metal-semiconductor transition like behavior of naphthalene-doped single wall carbon nanotube bundles.

Naphthalene (N) or naphthalene-derivative (ND) adsorption-treatment evidently varies the electrical conductivity of single wall carbon nanotube (SWCNT) bundles over a wide temperature range due to a charge-transfer interaction. The adsorption treatment of SWCNTs with dinitronaphthalene molecules enhances the electrical conductivity of the SWCNT bundles by 50 times. The temperature dependence of the electrical conductivity of N- or ND-adsorbed SWCNT bundles having a superlattice structure suggests metal-semiconductor transition like behavior near 260 K. The ND-adsorbed SWCNT gives a maximum in the logarithm of electrical conductivity vs. T(-1) plot, which may occur after the change to a metallic state and be associated with a partial unravelling of the SWCNT bundle due to an evoked librational motion of the moieties of ND with elevation of the temperature.

Clean nanotube unzipping by abrupt thermal expansion of molecular nitrogen: graphene nanoribbons with atomically smooth edges.

We report a novel physicochemical route to produce highly crystalline nitrogen-doped graphene nanoribbons. The technique consists of an abrupt N(2) gas expansion within the hollow core of nitrogen-doped multiwalled carbon nanotubes (CN(x)-MWNTs) when exposed to a fast thermal shock. The multiwalled nanotube unzipping mechanism is rationalized using molecular dynamics and density functional theory simulations, which highlight the importance of open-ended nanotubes in promoting the efficient introduction of N(2) molecules by capillary action within tubes and surface defects, thus triggering an efficient and atomically smooth unzipping. The so-produced nanoribbons could be few-layered (from graphene bilayer onward) and could exhibit both crystalline zigzag and armchair edges. In contrast to methods developed previously, our technique presents various advantages: (1) the tubes are not heavily oxidized; (2) the method yields sharp atomic edges within the resulting nanoribbons; (3) the technique could be scaled up for the bulk production of crystalline nanoribbons from available MWNT sources; and (4) this route could eventually be used to unzip other types of carbon nanotubes or intercalated layered materials such as BN, MoS(2), WS(2), etc.