Influence of Thin Film Deposition on AFM Cantilever Tips in Adhesion and Young's Modulus of MEMS Surfaces.

Adhesion is a critical factor in microelectromechanical systems (MEMSs) and is influenced by many parameters. In important fields, such as microassembly, an improved understanding of adhesion can result in higher precision. This study examines the influence of deposition of gold and titanium onto the atomic force microscope (AFM) tips in adhesion forces and Young's modulus, between a few MEMS substrates (silicon, gold, and silver) and the AFM tips. It was found that, except for gold substrate, an AFM tip coated with gold has the highest adhesion force of 42.67 nN for silicon substrates, whereas the titanium-coated AFM tip decreases the force for all the samples. This study suggests that such changes must be taken into account while studying the adhesion force. The final results indicate that utilizing gold substrate with titanium AFM tip led to the lowest adhesion force, which could be useful in adhesion force measurement during microassembly.

Nitrates Removal from Simulated Groundwater Using Nano Zerovalent Iron Supported by Polystyrenic Gel.

The main objectives of this present paper were to indicate the immobilization of nano zerovalent iron (nZVI) onto a polymeric material (Purolite A400) and the synthesis of the polymeric material (A400-nZVI) through sodium borohydride (NaBH4) reduction. The obtained polymeric material (A400-nZVI) was used for the nitrate ions removal from a simulated groundwater at different conditions. The polymeric materials, without and with nano zerovalent iron (A400 and A400-nZVI), were characterized trough the FTIR, SEM-EDAX, XRD, and TGA analysis. The analysis confirmed the presence of nano zerovalent iron (nZVI) onto the polymeric material (A400). The adsorption capacity of A400-nZVI, used as polymeric adsorbent, was evaluated by kinetic and thermodynamic studies. The obtained experimental results indicated that the nitrate ions reduction was fitted well by models: pseudo-second-order kinetic and Freundlich isotherm. According to the kinetic model results, a reaction mechanism could exist in the stage of reactions. The higher value of removal nitrate (>80%) was obtained under acidic condition. The results indicated that the obtained polymeric material (A400-nZVI) can be considered as a potential polymeric adsorbent for different pollutants from groundwater and wastewater.

Modified Composite Based on Magnetite and Polyvinyl Alcohol: Synthesis, Characterization, and Degradation Studies of the Methyl Orange Dye from Synthetic Wastewater.

The goal of the present paper was to synthesize, characterize, and evaluate the performance of the modified composite based on magnetite (Fe3O4) and polyvinyl alcohol (PVA). The obtained composite was used to degrade Methyl Orange dye from synthetic wastewater by a laboratory photocatalytic reactor. Various parameters of the photodegradation process were tested: composite dosage, amount of hydrogen peroxide (H2O2), and pH. The composite was characterized by Fourier Transform Infrared (FTIR) Spectroscopy, X-ray Diffraction (XRD), and Scanning Electron Microscopy (SEM). The degradation experiments indicated that the complete dye decolorization depended on the amount of H2O2. In addition, the H2O2 could accelerate Methyl Orange degradation to more highly oxidized intermediates in the presence of UV light (99.35%). The results suggested that the obtained modified composite could be used to treat wastewater containing various types of dyes.

Study of Polyvinyl Alcohol-SiO2 Nanoparticles Polymeric Membrane in Wastewater Treatment Containing Zinc Ions.

The main goal of the present paper was to synthesize the polyvinyl alcohol-SiO2 nanoparticles polymeric membrane by wet-phase inversion method. The efficiency of prepared membranes (without and with SiO2) was investigated using a versatile laboratory electrodialysis system filled with simulated wastewaters that contain zinc ions. All experiments were performed at following conditions: the applied voltage at electrodes of 5, 10 and 15 V, a concentration of zinc ions solution of 2 g L-1, time for each test of 1 h and at room temperature. The demineralization rate, extraction percentage of zinc ions, current efficiency and energy consumption were determined. The polymeric membranes were characterized by Fourier Transforms Infrared Spectroscopy-Attenuated Total Reflection (FTIR-ATR), Scanning Electron Microscopy (SEM) and Electrochemical Impedance Spectroscopy (EIS). The higher value of percentage removal of zinc ions (over 65%) was obtained for the polymeric membrane with SiO2 nanoparticles, at 15 V. The FTIR-ATR spectra show a characteristic peak located at ~1078 cm-1 assigned to the Si-O-Si asymmetrical stretching. SEM images of the polymeric membrane with SiO2 nanoparticles show that the nanoparticles and polymer matrix were well compatible. The impedance results indicated that the SiO2 nanoparticles induced the higher proton conductivity. The final polymeric membranes can be used for the removal of various metallic ions, dyes, organic or inorganic colloids, bacteria or other microorganisms from different natural waters and wastewaters.

Fungal Based Biopolymer Composites for Construction Materials.

Environmental contamination, extensive exploitation of fuel sources and accessibility of natural renewable resources represent the premises for the development of composite biomaterials. These materials have controlled properties, being obtained through processes operated in mild conditions with low costs, and contributing to the valorization of byproducts from agriculture and industry fields. A novel board composite including lignocelullosic substrate as wheat straws, fungal mycelium and polypropylene embedded with bacterial spores was developed and investigated in the present study. The bacterial spores embedded in polymer were found to be viable even after heat exposure, helping to increase the compatibility of polymer with hydrophilic microorganisms. Fungal based biopolymer composite was obtained after cultivation of Ganoderma lucidum macromycetes on a mixture including wheat straws and polypropylene embedded with spores from Bacillus amyloliquefaciens. Scanning electron microscopy (SEM) and light microscopy images showed the fungal mycelium covering the substrates with a dense network of filaments. The resulted biomaterial is safe, inert, renewable, natural, biodegradable and it can be molded in the desired shape. The fungal biocomposite presented similar compressive strength and improved thermal insulation capacity compared to polystyrene with high potential to be used as thermal insulation material for applications in construction sector.

Preparation and Characterization of Silica Nanoparticles and of Silica-Gentamicin Nanostructured Solution Obtained by Microwave-Assisted Synthesis.

In this research work, silica nanoparticles and silica-gentamicin nanostructured solution were synthesized by using the microwave-assisted synthesis, in basic medium, using two silane precursors (tetraethylorthosilicate and octyltriethoxysilane) and the antibiotic (gentamicin sulfate). The prepared materials were characterized through Fourier transform infrared (FTIR) spectroscopy, TGA analysis, transmission electron microscopy (TEM), and atomic force microscopy (AFM) to investigate the morphology and structure. Antimicrobial studies of the silica-gentamicin nanostructured solution versus silica nanoparticles were performed against Pseudomonas aeruginosa, Staphylococcus aureus, and Escherichia coli. FTIR spectra showed that the gentamicin has been loaded to the silica nanoparticles. AFM analysis showed that the morphology of the silica-gentamicin nanostructured solution has changed, and agglomerations of particles are present at the surface. Antimicrobial testing, performed using the diffusion method through spot inoculation, indicates that the silica-gentamicin nanostructured solution exhibited activity against the resistant strain. The obtained silica-gentamicin solution can be used as biochemical agent for the prevention and treatment of microorganisms which are deposited on different surfaces (e.g., glass, plastic, ceramic).

Modeling the Properties of Curcumin Derivatives in Relation to the Architecture of the Siloxane Host Matrices.

Research in the field of natural dyes has constantly focused on methods of conditioning curcumin and diversifying their fields of use. In this study, hybrid materials were obtained from modified silica structures, as host matrices, in which curcumin dyes were embedded. The influence of the silica network structure on the optical properties and the antimicrobial activity of the hybrid materials was monitored. By modifying the ratio between phenyltriethoxysilane:diphenyldimethoxysilane (PTES:DPDMES), it was possible to evaluate the influence the organosilane network modifiers had on the morphostructural characteristics of nanocomposites. The nanosols were obtained by the sol-gel method, in acid catalysis. The nanocomposites obtained were deposited as films on a glass support and showed a transmittance value (T measured at 550 nm) of around 90% and reflectance of about 11%, comparable to the properties of the uncovered support. For the coatings deposited on PET (polyethylene terephthalate) films, these properties remained at average values of T550 = 85% and R550 = 11% without significantly modifying the optical properties of the support. The sequestration of the dye in silica networks reduced the antimicrobial activity of the nanocomposites obtained, by comparison to native dyes. Tests performed on Candida albicans fungi showed good results for the two curcumin derivatives embedded in silica networks (11-18 mm) by using the spot inoculation method; in comparison, the alcoholic dye solution has a spot diameter of 20-23 mm. In addition, hybrids with the CA derivative were the most effective (halo diameter of 17-18 mm) in inhibiting the growth of Gram-positive bacteria, compared to the curcumin derivative in alcoholic solution (halo diameter of 21 mm). The results of the study showed that the presence of 20-40% by weight DPDMES in the composition of nanosols is the optimal range for obtaining hybrid films that host curcumin derivatives, with potential uses in the field of optical films or bioactive coatings.

Mixed Oxide Layered Double Hydroxide Materials: Synthesis, Characterization and Efficient Application for Mn2+ Removal from Synthetic Wastewater.

Magnesium-aluminum (Mg-Al) and magnesium-aluminum-nickel (Mg-Al-Ni) layered double hydroxides (LDHs) were synthesized by the co-precipitation method. The adsorption process of Mn2+ from synthetic wastewater was investigated. Formation of the layered double hydroxides and adsorption of Mn2+ on both Mg-Al and Mg-Ni-Al LDHs were observed by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy Dispersive Spectrometry (EDX) analysis. XRD patterns for prepared LDHs presented sharp and symmetrical peaks. SEM studies revealed that Mg-Al LDH and Mg-Al-Ni LDH exhibit a non-porous structure. EDX analysis showed that the prepared LDHs present uniformly spread elements. The adsorption equilibrium on these LDHs was investigated at different experimental conditions such as: Shaking time, initial Mn2+ concentration, and temperatures (10 and 20 °C). The parameters were controlled and optimized to remove the Mn2+ from synthetic wastewater. Adsorption isotherms of Mn2+ were fitted by Langmuir and Freundlich models. The obtained results indicated that the isotherm data fitted better into the Freundlich model than the Langmuir model. Adsorption capacity of Mn2+ gradually increased with temperature. The Langmuir constant (KL) value of Mg-Al LDH (0.9529 ± 0.007 L/mg) was higher than Mg-Al-Ni LDH (0.1819 ± 0.004 L/mg), at 20 °C. The final adsorption capacity was higher for Mg-Al LDH (91.85 ± 0.087%) in comparison with Mg-Al-Ni LDH (35.97 ± 0.093%), at 20 °C. It was found that the adsorption kinetics is best described by the pseudo-second-order model. The results indicated that LDHs can be considered as a potential material for adsorption of other metallic ions from wastewater.

Biopolymeric Membrane Enriched with Chitosan and Silver for Metallic Ions Removal.

The present paper synthesized, characterized, and evaluated the performance of the novel biopolymeric membrane enriched with cellulose acetate and chitosan (CHI)-silver (Ag) ions in order to remove iron ion from the synthetic wastewater using a new electrodialysis system. The prepared membranes were characterized by Fourier Transforms Infrared Spectroscopy-Attenuated Total Reflection (FTIR-ATR), Thermal Gravimetric Analysis (TGA) and Differential Thermal Analysis (DSC), contact angle measurements, microscopy studies, and electrochemical impedance spectroscopy (EIS). The electrodialysis experiments were performed at the different applied voltages (5, 10, and 15 V) for one hour, at room temperature. The treatment rate (TE) of iron ions, current efficiency (IE), and energy consumption (Wc) were calculated. FTIR-ATR spectra evidenced that incorporation of CHI-Ag ions into the polymer mixture led to a polymer-metal ion complex formation within the membrane. The TGA-DSC analysis for the obtained biopolymeric membranes showed excellent thermal stability (>350 °C). The contact angle measurements demonstrated the hydrophobic character of the polymeric membrane and a decrease of it by CHI-Ag adding. The EIS results indicated that the silver ions induced a higher ionic electrical conductivity. The highest value of the iron ions treatment rate (>60%) was obtained for the biopolymeric membrane with CHI-Ag ions at applied voltage of 15 V.

Drug Delivery System Based on pH-Sensitive Biocompatible Poly(2-vinyl pyridine)-b-poly(ethylene oxide) Nanomicelles Loaded with Curcumin and 5-Fluorouracil.

Smart polymeric micelles (PMs) are of practical interest as nanocarriers for the encapsulation and controlled release of hydrophobic drugs. Two hydrophobic drugs, naturally-based curcumin (Cur) and synthetic 5-fluorouracil (5-FU), were loaded into the PMs formed by a well-defined pH-sensitive poly(2-vinyl pyridine)-b-poly(ethylene oxide) (P2VP90-b-PEO398) block copolymer. The influence of the drug loading on the micellar sizes was investigated by dynamic light scattering (DLS) and it appears that the size of the PMs increases from around 60 to 100 nm when Cur is loaded. On the contrary, the loading of the 5-FU has a smaller effect on the micellar sizes. This difference can be attributed to higher molar mass of Cur with respect to 5-FU but also to higher loading efficiency of Cur, 6.4%, compared to that of 5-FU, 5.8%. In vitro drug release was studied at pH 2, 6.8, and 7.4, and it was observed that the pH controls the release of both drugs. At pH 2, where the P2VP sequences from the "frozen-in" micellar core are protonated, the drug release efficiencies exceed 90%. Moreover, it was demonstrated, by in vitro assays, that these PMs are hemocompatible and biocompatible. Furthermore, the PMs protect the Cur against the photo-degradation, whereas the non-ionic PEO corona limits the adsorption of bovine serum albumin (BSA) protein on the surface. This study demonstrates that these pH-sensitive PMs are suitable for practical utilization as human-safe and smart, injectable drug delivery systems.

The Effect of Different Coupling Agents on Nano-ZnO Materials Obtained via the Sol-Gel Process.

Hybrid nanomaterials based on zinc oxide were synthesized via the sol-gel method, using different silane coupling agents: (3-glycidyloxypropyl)trimethoxysilane (GPTMS), phenyltriethoxysilane (PhTES), octyltriethoxysilane (OTES), and octadecyltriethoxysilane (ODTES). Morphological properties and the silane precursor type effect on the particle size were investigated using dynamic light scattering (DLS), environmental scanning electron microscopy (ESEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), and X-ray diffraction (XRD). The bonding characteristics of modified ZnO materials were investigated using Fourier transform infrared spectroscopy (FTIR). The final solutions were deposited on metallic substrate (aluminum) in order to realize coatings with various wettability and roughness. The morphological studies, obtained by ESEM and TEM analysis, showed that the sizes of the ZnO nanoparticles are changed as function of silane precursor used in synthesis. The thermal stability of modified ZnO materials showed that the degradation of the alkyl groups takes place in the 300-500 °C range. Water wettability study revealed a contact angle of 142 ± 5° for the surface covered with ZnO material modified with ODTES and showed that the water contact angle increases as the alkyl chain from the silica precursor increases. These modified ZnO materials, therefore, can be easily incorporated in coatings for various applications such as anti-corrosion and anti-icing.

The Influence of New Hydrophobic Silica Nanoparticles on the Surface Properties of the Films Obtained from Bilayer Hybrids.

Ultra-hydrophobic bilayer coatings on a glass surface were fabricated by sol-gel process using hexadecyltrimethoxysilane (C16TMS) and tetramethoxysilane (TMOS) (1:4 molar ratio) as precursors. After coating, silica nanoparticles (SiO2 NPs) functionalized with different mono-alkoxy derivatives (methoxytrimethylsilane, TMeMS; ethoxydimethylvinylsilane, DMeVES; ethoxydimethylphenylsilane, DMePhES; and methoxydimethyloctylsilane, DMeC8MS) were added, assuring the microscale roughness on the glass surface. Influences of the functionalized SiO2 NPs and surface morphology on the hydrophobicity of the hybrid films were discussed. The successful functionalization of SiO2 NPs with hydrophobic alkyl groups were confirmed by Fourier transform infrared spectroscopy (FTIR). The thermal stability of hydrophobic SiO2 NPs showed that the degradation of the alkyl groups takes place in the 200-400 °C range. Bilayer coating with C16TMS/TMOS and SiO2 NPs modified with alkoxysilane substituted with C8 alkyl chain (SiO2 NP-C8) has micro/nano structure. Hydrophobicity of functionalized SiO2 NPs-C8 and its higher degree of nanometer-scale roughness gave rise to ultra-hydrophobicity performance for bilayer coating C16TMS/TMOS + SiO2 NPs-C8 (145°), compared to other similar hybrid structures. Our synthesis method for the functionalization of SiO2 NPs is useful for the modification of surface polarity and roughness.

Efficient removal of Indigo Carmine dye by a separation process.

This study is aimed at developing an innovative approach for Indigo Carmine dye removal from synthetic solutions by electrodialysis, carried out using ion exchange membranes. The batch electrodialysis system was operated at various current intensities: 0.05, 0.1 and 0.15 A. The pH and conductivity of solutions were measured before and after using electrodialysis process. The colour removal efficiency (CR %) was determined by spectrographic analysis and the energy consumption (EC) was calculated. The obtained results show that the pH of treated solution increases due to the increase in solution conductivity. Moreover, the values of CR % and EC increase when increasing current intensity. The optimal value was obtained at 0.15 A (CR > 97%). The membranes were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis and scanning electron microscopy.

Synthesis of Non-Toxic Silica Particles Stabilized by Molecular Complex Oleic-Acid/Sodium Oleate.

The present work is focused on the preparation of biocompatible silica particles from sodium silicate, stabilized by a vesicular system containing oleic acid (OLA) and its alkaline salt (OLANa). Silica nanoparticles were generated by the partial neutralization of oleic acid (OLA), with the sodium cation present in the aqueous solutions of sodium silicate. At the molar ratio OLA/Na⁺ = 2:1, the molar ratio (OLA/OLANa = 1:1) required to form vesicles, in which the carboxyl and carboxylate groups have equal concentrations, was achieved. In order to obtain hydrophobically modified silica particles, octadecyltriethoxysilane (ODTES) was added in a sodium silicate sol-gel mixture at different molar ratios. The interactions between the octadecyl groups from the modified silica and the oleyl chains from the OLA/OLANa stabilizing system were investigated via simultaneous thermogravimetry (TG) and differential scanning calorimetry (DSC) (TG-DSC) analyses.A significant decrease in vaporization enthalpy and an increase in amount of ODTES were observed. Additionally, that the hydrophobic interaction between OLA and ODTES has a strong impact on the hybrids' final morphology and on their textural characteristics was revealed. The highest hydrodynamic average diameter and the most negative ζ potential were recorded for the hybrid in which the ODTES/sodium silicate molar ratio was 1:5. The obtained mesoporous silica particles, stabilized by the OLA/OLANa vesicular system, may find application as carriers for hydrophobic bioactive molecules.

San copolymer membranes with ion exchangers for Cu(II) removal from synthetic wastewater by electrodialysis.

Heterogeneous membranes were obtained by using styrene-acrylonitrile copolymer (SAN) blends with low content of ion-exchanger particles (5wt.%). The membranes obtained by phase inversion were used for the removal of copper ions from synthetic wastewater solutions by electrodialytic separation. The electrodialysis was conducted in a three cell unit, without electrolyte recirculation. The process, under potentiostatic or galvanostatic control, was followed by pH and conductivity measurements in the solution. The electrodialytic performance, evaluated in terms of extraction removal degree (rd) of copper ions, was better under potentiostatic control then by the galvanostatic one and the highest (over 70%) was attained at 8V. The membrane efficiency at small ion-exchanger load was explained by the migration of resin particles toward the pores surface during the phase inversion. The prepared membranes were characterized by various techniques i.e. optical microscopy, Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis and differential thermal analysis and contact angle measurements.

On the photocatalytic reduction of MTT tetrazolium salt on the surface of TiO2 nanoparticles: Formazan production kinetics and mechanism.

HYPOTHESIS: The MTT [3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium-bromide] cell cytotoxicity indicator is photocatalytically reduced on the surface of TiO2 nanoparticles in phosphate-buffered-saline (PBS) environment. We hypothesize that specific phosphate adsorption may be used to modulate the efficiency of the TiO2-MTT reaction through colloidal and semiconductor-liquid interface processes. EXPERIMENTS: The TiO2-MTT reaction kinetics was studied in PBS, with respect to photocatalyst and MTT concentrations and irradiation wavelength. The effects of PBS and electron scavengers (Fe(3+) ions) on reaction efficiency and the role of colloidal surface charge in the photocatalytic process were investigated. The structural and spectroscopic characteristics of relevant TiO2-formazan systems were studied by X-ray diffraction, transmission electron microscopy and IR-spectroscopy. FINDINGS: The reaction was pseudo-first order with respect to photocatalyst and showed a negative and fractional partial order with respect to MTT. Formazan production rates were directly proportional to radiation wavelength and TiO2 concentration and inversely proportional to the MTT initial concentration. The addition of Fe(3+) ions, as well as the absence of PBS, induced strong reaction inhibition. Reaction efficiency and catalyst Zeta potential were enhanced by Na2HPO4 (PBS component) and showed a maximum around the phosphate concentration 0.005 M. Structural/spectroscopic characterization confirmed the formation of amorphous MTT-formazan on the surface of TiO2 and the TiO2-phosphate binding.