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Hydrophobic electrospun membranes have a lot of applications in different fields. It is very difficult to increase the hydrophobicity of membranes for a specific application. This study investigates the effects of various electrospinning parameters on the morphology and hydrophobicity of polystyrene (PS) electrospun membranes. Polystyrene fibers were used as a reference for the study. Different parameters such as polymer concentrations, diameter of needles, and applied voltage were tested to study the influence on the hydrophobicity of electrospun fibers. Polystyrene fibers were electrospun at different concentrations from 5 to 20 wt.%, needles with a diameter from 0.5 to 3 mm were used, and voltage was applied between 8.06-16.05 kV. The surface morphology of polystyrene fibers and hydrophobicity were studied with a scanning electronic microscope and contact angle measurements. Based on the results of the study, higher polymer concentrations and voltages produce thinner fibers and more hydrophobic membranes. The results of this paper can be applied to the fabrication of different characteristic membranes for specific applications like water conservation, purification, and other fields. [ABSTRACT FROM AUTHOR]

This study investigates the development of superhydrophobic coatings on microfiber surfaces, with a specific focus on cotton, tweed, felt, and polyester fabrics. The resulting coatings demonstrated significant hydrophobicity, with water contact angles ranging from 128.5° for polyester to 148.9° for tweed. In addition, this investigation delves into the influence of pH levels on water contact angles, revealing notable fluctuations; specifically, higher pH levels resulted in decreased contact angles. The results indicated that the tweed fabric had the highest water contact angle at 151.7°, observed at a pH of 4. This study not only underscores the effective hydrophobic performance of these coatings but also highlights their practical applications. In particular, the research demonstrates the potential use of superhydrophobic coatings in the construction of traditional Kazakh ui (yurts), especially emphasizing the promising water repellency properties of felt fibers. Furthermore, this research illustrates a promising approach for producing superhydrophobic coatings on various microfiber surfaces, underlining their extensive potential applications within the textile industry. Overall, the findings suggest that the innovative use of superhydrophobic coatings can significantly enhance the water resistance of traditional and modern fabrics, paving the way for their broader application in various industries, including outdoor textiles and protective clothing. [ABSTRACT FROM AUTHOR]

In this work, hierarchical WO3 microspheres were synthesized using chemical bath deposition. The morphology of the synthesized sample was studied using scanning electron microscopy (SEM). The hierarchical WO3 microspheres formed from spontaneously self-assembled nanosheets have a high specific surface area. Structural characterizations of sample were performed using X-ray diffraction (XRD) and Raman spectroscopy. Analysis of XRD spectra showed that synthesized particles have a monoclinic modification. The optical properties of the sample were studied using UV-Vis diffuse reflectance absorption spectra. The value of the energy gap calculated from the absorption spectra is 2.25 eV, which indicates high light absorption ability. A photocurrent study was done to investigate the photocatalytic activity. The photoelectrode was prepared using hierarchical WO3 microspheres and polymer deposited on fluorine doped tin oxide (FTO) glass via spin coating technique. A remarkable photocurrent density of 18 A/cm2 at 0.5 V was achieved. The elongated structures improved light absorption ability and photocatalytic activity, and might be perspective as photoanode in photoelectrochemical cells. [ABSTRACT FROM AUTHOR]

The Crude Distillation Unit (CDU) mechanism is commonly regarded as the first stage in petroleum refining. In this study, Aspen Plus® is used to simulate the basic process of a CDU, which consists of an Atmospheric Distillation Column (ATC) and a Vacuum Distillation Column (VC). These columns are fed with two types of crude oil: KUMKOL from Kazakhstan and Soviet Export Blend, in the proportions of 0.75:0.25, 0.50:0.50, and 0.25:0.75, respectively. The goal was to do a parametric analysis and analyze the resultant streams of naphtha, kerosene, Atmospheric Gas Oil (AGO), Light Vacuum Gas Oil (LVGO), and Heavy Vacuum Gas Oil (HVGO). The simulation used the CHAO-SEA thermodynamic model, which included the Chao-Seader correlation, the Scatchard-Hildebrand model, the Redlich-Kwong equation of state, the Lee-Kesler equation of state, and the API gravity technique. Temperature, pressure, mass flow, enthalpy, vapor percentage, and average molecular weights of the streams at various phases within the CDU system were estimated. For both the ATC and VC columns, curves indicating Temperature-Pressure vs the number of stages, as well as ASTM D86 (temperature) versus stream volume % distillation, were developed. The results show that when compared to feed streams containing 0.25 and 0.50 StdVol of Kumkol Kazakhstan Oil, the feed stream with 0.75 StdVol produces more Heavy, Medium, and Light Vacuum Gas Oil (H-VGO, M-VGO, and L-VGO), as well as more Vacuum Gas (VG). These findings indicate that Kumkol Kazakhstan Oil is of high quality and has fewer contaminants, such as sulfur when compared to other accessible mixes throughout the world. [ABSTRACT FROM AUTHOR]

In this study, the effect of modification of poly(3,4‐ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) morphology on its optical, charge transport, and photovoltaic properties of organic solar cells based on the P3HT:PC60BM bulk heterojunction is presented. It is shown that the addition of isopropyl alcohol to the PEDOT:PSS polymer solution and annealing of spin‐coated PEDOT:PSS film leads to a change in its morphology, charge transport, and optical properties. By an impedance spectroscopy technique, the charge transport properties of PEDOT:PSS films were studied. It was established that the efficiency of carrier transport and the efficiency of the polymer solar cells depends on the structural features of PEDOT:PSS. [ABSTRACT FROM AUTHOR]

Flocculants are widely investigated chemicals, which can be utilized to remedy or purify waste water from industries including petroleum, fabric, mining. Although many types of flocculants have been explored, each flocculant has it's merits and demerits. Thus, we investigated poly (N,N-diallyl-N,Ndimethylammonium chloride) cationic flocculants. This work reports a novel flocculant which was developed based on the widely used flocculant, poly (N,N-diallyl-N,N-dimethylammonium chloride) (DADMAC) cationic polymers. This newly developed flocculant has not only enhanced flocculant performance, but also provided reusability of this polymer with insertion of crosslinking groups. The new developed copolymer, Poly (DADMAC-co- VEMEA), was synthesized via random radical polymerization approach and characterized by NMR and FTIR. The flocculation performance for these polymers were evaluated and studied by turbidity experiments and zeta-potential measurements. Their flocculation performance over poly (DADMAC) homopolymer can be improved by adding a VEMEA unit to the polymer chain and partially crosslinking the copolymer. This newly developed flocculant can provide new direction in developing flocculants potentially. [ABSTRACT FROM AUTHOR]

Polyaniline (PANI)-based supercapacitors suffer from environmental and mechanical instabilities. In this work, a novel bicontinuous microemulsion approach was developed to fabricate a unique nanofibre structure of polyaniline and its 3D-crosslinked network using crosslinking chemistry, which improved both the mechanical and electrochemical performance of a PANI-based supercapacitor. The polyaniline nanofibers and its 3D-crosslinked networks produced by bicontinuous nanoreactors were investigated using experimental tools, such as SEM, FTIR, BET, TGA and DSC. Electrochemical evaluations for the above polyaniline nanofibers and its 3D-crosslinked materials was performed via cyclic voltammetry and galvanostatic charge-discharge measurements. The result of this study demonstrated that the PANI nanofiber exhibited the highest specific capacitance of 280.4 F g -1 at a current density of 1 A g -1 , while both PANI-based supercapacitors made of nanofibers and 3D-crosslinked materials retained good cycling stability of 98% during continuous redox cycling., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

Zwitterionic polymers have garnered significant attention for their distinctive properties, such as biocompatibility, antifouling capabilities, and resistance to protein adsorption, making them promising candidates for a wide range of applications, including drug delivery, oil production inhibitors, and water purification membranes. This study reports the synthesis and characterization of zwitterionic monomers and polymers through the modification of linear, vinyl, and aromatic heterocyclic functional groups via reaction with 1,3-propanesultone. Four zwitterionic polymers with varying molecular structures-ranging from linear to five and six membered ring systems-were synthesized: poly(sulfobetaine methacrylamide) (pSBMAm), poly(sulfobetaine-1-vinylimidazole) (pSB1VI), poly(sulfobetaine-2-vinylpyridine) (pSB2VP), and poly(sulfobetaine-4-vinylpyridine) (pSB4VP). Their molecular weights, thermal behavior, and self-assembly properties were analyzed using gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), transmission electron microscopy (TEM), and zeta potential measurements. The glass transition temperatures (Tg) ranged from 276.52 °C for pSBMAm to 313.69 °C for pSB4VP, while decomposition temperatures exhibited a similar trend, with pSBMAm degrading at 301.03 °C and pSB4VP at 387.14 °C. The polymers' self-assembly behavior was strongly dependent on pH and their surface charge, particularly under varying pH conditions: spherical micelles were observed at neutral pH, while fractal aggregates formed at basic pH. These results demonstrate that precise modifications of the chemical structure, specifically in the linear, imidazole, and pyridine moieties, enable fine control over the thermal properties and self-assembly behavior of polyzwitterions. Such insights are essential for tailoring polymer properties for targeted applications in filtration membranes, drug delivery systems, and solid polymer electrolytes, where thermal stability and self-assembly play crucial roles.

The hydrogen (H 2 ) energy industry has continued to expand in recent years due to the decarbonization of the global energy system and the drive towards sustainable development. Due to hydrogen's high flammability and significant safety risks, the efficient detection of hydrogen has become an increasingly hot issue today. In this work, a new type of relatively fast and responsive conducting polymer sensor has been demonstrated for tracing H 2 gas in a nitrogen environment. Inspiration of unique properties of carbon nanotube (CNT) and graphene, polyaniline (PANI) hollow nanotubes, PANI thin films are fabricated to study for structural-properties investigation. The PANI hollow nanotube sensor ensures the 1 ppm hydrogen gas detection at room temperature, and exhibits high sensitivity (29%) and fast response and recovery times of 15 and 17 s, follows by PANI thin film sensor (20%), response and recovery times of 65s and 45s. This conducting polymer-based hydrogen sensor holds promise for the early detection of H 2 leaks in a wide range of industries., (© 2024. The Author(s).)

The removal of sulfur compounds, particularly thiophene derivatives, from oil is crucial due to concerns about environmental issues. Therefore, the deep desulfurization of transportation fuels is currently an urgent problem, and numerous attempts have been made in this direction. Membrane-based desulfurization can be a good alternative to the traditional hydrodesulfurization method, which has several limitations. In this work, the use of membranes containing a metal-organic framework, MOF-5, doped with transition metals (Ag, Cu, Ni), in the adsorptive desulfurization process was studied. The efficiency of membranes was evaluated based on selective removal of thiophene and dibenzothiophene from model oil. Characterization techniques, including scanning electron microscopic (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA), confirmed the successful synthesis and incorporation of metal-organic frameworks (MOFs) into mixed matrix membranes (MMMs). Desulfurization experiments showed that MOF-5/Ag exhibited the highest thiophene adsorption efficiency (86.8%), outperforming MOF-5/Cu and MOF-5/Ni. The enhanced performance is attributed to the strong interaction between silver and sulfur. These findings demonstrate the potential of MOF-based MMMs for efficient and selective desulfurization, offering a viable alternative to traditional hydrodesulfurization (HDS) methods., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

In this report, 38 nm-thick amorphous zinc-tin oxide (a-ZTO) films were deposited by radio frequency magnetron cosputtering. a-ZTO films were annealed by in situ monitoring of the sheet resistance improvements during the annealing process. A sharp drop in the slope of the sheet resistance curve was observed. The activation energies for the sheet resistance slope were calculated. The activation energy of the reaction for a sharp drop in the slope is much higher than the activation energy for the rest of the slope. Based on the activation energy values, six annealing temperatures were selected to saturate the highest conductivity at lower annealing temperatures and to identify the effects associated with annealing time. We found a direct correlation between annealing temperatures and the duration of the annealing treatment. a-ZTO films with a high conductivity of 320 S/cm were achieved by annealing at a temperature of 220 °C. It is noteworthy that the annealing temperature of 220 °C has clearly replaced the temperature of 300 °C. An irreversible decrease in resistivity was observed for all films. The conduction mechanism of films before and after annealing was determined. We confirm that all films individually exhibit semiconducting and metallic behaviors in the conduction mechanism before and after the lowest resistivity saturation., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

A comparative study of the plasmon effect of Ag and Au nanoparticles on TiO 2 /rGO nanocomposite was carried out. The synthesis of Au and Ag nanoparticles was carried out by laser ablation. The morphology and structure of the nanocomposites were studied by EDA, HRTEM, XRD and Raman spectroscopy. It was shown that the absorption capacity of the nanocomposite material was increased in the visible range of the spectrum when Ag and Au nanoparticles were added to TiO 2 /rGO. This leads to an increase in their photocatalytic activity. The photocurrent generated by NC/Au 10 -11 films is in 3.8 times and NC/Ag 10 -12 is in 2 times higher compared to pure TiO 2 /rGO film. Similar results were obtained from experimental data on the dyes photodegradation. In the presence of plasmon nanoparticles a significant enhancement in the electrical properties of the TiO 2 /rGO nanocomposite was recorded. The charge carrier transfer resistance in nanocomposites was decreased by almost ∼7 times for NC/Au,10 -11 and ∼4 times for NC/Ag,10 -12 films compared to pure TiO 2 /rGO. In addition, for nanocomposites with Ag or Au nanoparticles, a decrease in the effective electron lifetime was observed. The data obtained allow us to conclude that plasmonic NPs have a synergistic effect in TiO 2 /rGO nanocomposites, which consists in modifying both their light-harvesting properties and charge-transport characteristics. The results obtained can be used for the design of materials with improved photocatalytic and optoelectronic characteristics., (© 2024 IOP Publishing Ltd.)

Versatile nanostructures of conducting polymers are highly relevant based on unique properties, including electrical, optical, and thermal, with changes in morphology. This contribution reports a facile and reproducible synthesis approach for the design of conducting polymer nanostructures from zero- to three-dimensional composites. Two polymerization steps, namely, self-assembly-directed and interface thin layer-templated polymerizations in this synthesis, were kinetically controlled to fabricate such nanostructures directly. The uniquely designed bicontinuous nanoreactor offers an easy synthesis technique for fabricating 3D multifunctional conducting polymer composites. Self-assembly-directed polymerization could be controlled to form nanorods and further directed to form nanobowl/hollow spherical structures. The interface thin layer template process was tuned to produce hollow spherical and 2D film nanostructures. Kinetic control of polymerization was able to provide access to unprecedented nanostructures of the conducting polymers ranging from DNA origami to gecko-inspired nanostructures, with potential applications in drug delivery, energy storage, and adhesive materials. For example, this is the first conducting polymer material that can demonstrate similar adhesiveness (around 8 N/cm 2 ) to gecko finger hairs.

In recent decades, there has been a great deal of interest in conducting polymers due to their broad applications. At the same time, various synthetic techniques have been developed to produce various nanostructures of the conducting polymers with their fascinating properties. However, the techniques for the manufacture of 2D nanosheets are either complex or expensive. No comprehensive approach for constructing 2D and 3D materials or their composites has been documented. Herein, a simple and scalable synthetic protocol is reported for the design of 2D, 3D, and related conducting polymer nanocomposites by interface manipulation in a bicontinuous microemulsion system. In this method, diverse bicontinuous thin layers of oil and water are employed to produce 2D nanosheets of conducting polymers. For the fabrication of 3D polypyrrole (PPY) and their composites, specially designed linkers of the monomers are applied to lock the 3D networks of the conducting polymers and their composites. The technique can be extended to the fabrication of most conducting polymer composites, being cost-effective and easily scalable. The optimum electrical conductivity obtained for 2D PPY nanosheets is 219 S cm -1 , the highest literature value reported to date to the best of knowledge., (© 2022 The Authors. Advanced Materials published by Wiley-VCH GmbH.)

Catalytic conversion of biomass or biomass-derived intermediate to value-added chemicals is important for both biomass waste management and production of industrially important chemicals. Oxidation of 5-hydroximethyl furfural (HMF) is considered one of the most important biomass conversion processes, which resulted in many value-added products such as 2,5-diformylfuran (DFF), 2,5-furandicarboxylic acid (FDCA), 5-hydroxymethyl-2-furancarboxylic acid (HMFCA), and 5-formyl-2-furancarboxylic acid (FFCA). In this study, the three morphologies of CdS catalyst (nanorod, nanosheet, and nanosphere) with two different crystalline structures are synthesized and characterized by SEM, TEM, and XRD analysis. The oxidation of HMF to FFCA is performed using the synthesized catalysts in the presence of different solvents and oxidizing agents. We find that CdS nanorod provides the selective oxidation of HMF to FFCA in the presence of dimethyl sulfoxide solvent and tert -butyl hydrogen peroxide oxidizing agent. The density functional theory (DFT) simulations are carried out to explain the catalytic activity of the CdS catalyst for oxidation of HMF to FFCA. The DFT simulations show that CdS is an excellent catalyst for binding HMF on the CdS surface. Our findings provide the way of effective oxidation of biomass into value-added products using the cheap CdS catalyst.

This review focuses on tungsten oxide (WO 3 ) and its nanocomposites as photoactive nanomaterials for photoelectrochemical cell (PEC) applications since it possesses exceptional properties such as photostability, high electron mobility (~12 cm 2 V -1 s -1 ) and a long hole-diffusion length (~150 nm). Although WO 3 has demonstrated oxygen-evolution capability in PEC, further increase of its PEC efficiency is limited by high recombination rate of photogenerated electron/hole carriers and slow charge transfer at the liquid-solid interface. To further increase the PEC efficiency of the WO 3 photocatalyst, designing WO 3 nanocomposites via surface-interface engineering and doping would be a great strategy to enhance the PEC performance via improving charge separation. This review starts with the basic principle of water-splitting and physical chemistry properties of WO 3 , that extends to various strategies to produce binary/ternary nanocomposites for PEC, particulate photocatalysts, Z-schemes and tandem-cell applications. The effect of PEC crystalline structure and nanomorphologies on efficiency are included. For both binary and ternary WO 3 nanocomposite systems, the PEC performance under different conditions-including synthesis approaches, various electrolytes, morphologies and applied bias-are summarized. At the end of the review, a conclusion and outlook section concluded the WO 3 photocatalyst-based system with an overview of WO 3 and their nanocomposites for photocatalytic applications and provided the readers with potential research directions.

Heterostructured photocatalysts are superior to single photocatalysts because they offer better charge separation and broaden light harnessing abilities. Although WO 3 is considered an oxygen-evolving photocatalyst with decent stability and proper band gap, its lower photocatalytic efficiency is ascribed to high charge recombination. In this research, a WO 3 @Co 3 O 4 heterostructure reduced the recombination of photocatalytic charges and extended light absorption abilities, resulting in improved photocatalytic activity. The presence of Co 3 O 4 nanoparticles improved light absorption and charge transfer of tungsten oxide films for photoelectrochemical reactions. For photoelectrochemical water oxidation, WO 3 @Co 3 O 4 nanostructures generated a photocurrent 20 times higher than that of pure WO 3 . Both electrodeposition and sol gel techniques were utilized to synthesize the WO 3 @Co 3 O 4 photoelectrode. Scanning electron microscopy and X-ray diffraction were used to characterize the formation of the above photocatalyst. A photocurrent study was done to investigate the charge separation mechanism to explain the enhanced photocatalytic activity.

Heterostructure formation is an effective method used for designing photocatalysts that solve problems caused by photoexcited charge recombination phenomena associated with the photocatalytic water redox reaction. This work reports a new Co-metal-incorporated ternary heterostructured photocatalyst, CdS/CoO x /Co-metal, which enhanced charge separation to increase photocatalytic H 2 evolution 30.5-fold in comparison to pure CdS under visible light. This work demonstrates for the first time the effect of the Co metal on photocatalytic H 2 evolution using the CdS/CoO x /Co-metal ternary heterostructure. In the ternary heterostructure, Co metal and CoO x act as photogenerated electron- and hole-capturing cocatalysts, respectively. Results from photoelectrochemical studies along with photocatalytic H 2 evolution data proved the enhancement of charge transfer and separation in the CdS/CoO x /Co-metal heterostructure due to the addition of Co metal and CoO x . Hence, the synergistic charge separation improvement achieved by the combination of CoO x and the Co metal with CdS produced a photocatalytic H 2 evolution rate of 9.54 μmol/h, which is the highest reported H 2 evolution rate for a CdS-based system under l sun solar irradiance (>420 nm) to the best of our knowledge.

In this work, we report the first molecular weight-controlled amphiphilic polybetaine synthesis using various hydrocarbons via reversible addition?fragmentation chain-transfer (RAFT) polymerization. The experimental separation of the alkyl aminocrotonate tautomers, which has been the subject of debate, was completed for the first time. The enamine form of these tautomers was further used as a monomer for the RAFT polymerization of amphiphilic polycarboxybetaines. Self-assembly of the amphiphilic polycarboxybetaines showed micelle structures from spherical, rod-like to fractal in the aqueous media due to the competition between both electrostatic and hydrophobic forces. Hydrophobically dominant interactions among amphiphilic polycarboxybetaines and long-chain hydrocarbon alkane molecules were investigated to understand long-chain hydrocarbon alkane crystallization using alkane crystal deposition and viscosity experiments. Strong hydrophobic forces between poly(hexadecyl-grafted aminocrotonate?methacrylic acid) and long-chain hydrocarbon alkane molecules changed the surface properties of the long-chain hydrocarbon alkane nucleus and inhibited the growth of paraffin crystals.

Polybetaines have received widespread attention due to their smart response properties and structures which resemble biological polymers like peptides and DNA. However, few studies have focused on the controlled synthesis and self-assembly of hydrophobically modified polybetaines due to the difficulty of synthesizing these materials. We report the first molecular weight-controlled synthesis of hydrophobically modified polycarboxybetaines (HMPCB). Poly(dodecyl grafted aminocrotonate -methacrylic acid) (P(DACRO-MAA)) was synthesized via the reversible addition-fragmentation chain-transfer (RAFT) polymerization approach. The two different tautomers of the monomer were also successfully identified and separated via thin layer chromatography (TLC) and column chromatography, making it possible to obtain pure polycarboxybetaine via RAFT synthesis. Both the successfully separated enamine form of the monomer and the resulting polycarboxybetaine were confirmed via FTIR and NMR. The polycarboxybetaine was found to have a low polydispersity (PDI) of 1.214, and its molecular weight was determined as 70590 g/mol via gel permeation chromatography (GPC) measurements. Spherical, rodlike, and fractal assembled structures for the P(DACRO-MAA) were observed with pH change using TEM, zeta sizer, and dynamic light scattering (DLS). The unique self-assembled structures of HMPCB synthesized via RAFT provide an opportunity to understand fundamental polymer science and can be engineered for broad applications.

At present, a large amount of research from experimental and theoretical points of view has been done on interpolyelectrolyte complexes formed by electrostatic attractive forces and/or interpolymer complexes stabilized by hydrogen bonds. By contrast, relatively less attention has been given to polymer⁻polymer complex formation with synthetic polyampholytes (PA). In this review the complexation of polyampholytes with polyelectrolytes (PE) is considered from theoretical and application points of view. Formation of intra- and interpolyelectrolyte complexes of random, regular, block, dendritic polyampholytes are outlined. A separate subsection is devoted to amphoteric behavior of interpolyelectrolyte complexes. The realization of the so-called "isoelectric effect" for interpolyelectrolyte complexes of water-soluble polyampholytes, amphoteric hydrogels and cryogels with respect to surfactants, dye molecules, polyelectrolytes and proteins is demonstrated.

Polymeric nanofiber membranes of polyvinyl chloride (PVC) blended with polyvinylpyrrolidone (PVP) were fabricated using an electrospinning process at different conditions and used for the filtration of three different liquid suspensions to determine the efficiency of the filter membranes. The three liquid suspensions included lake water, abrasive particles from a water jet cutter, and suspended magnetite nanoparticles. The major goal of this research work was to create highly hydrophilic nanofiber membranes and utilize them to filter the suspended liquids at an optimal level of purification (i.e., drinkable level). In order to overcome the fouling/biofouling/blocking problems of the membrane, a coagulation process, which enhances the membrane's efficiency for removing colloidal particles, was used as a pre-treatment process. Two chemical agents, Tanfloc (organic) and Alum (inorganic), were chosen for the flocculation/coagulation process. The removal efficiency of the suspended particles in the liquids was measured in terms of turbidity, pH, and total dissolved solids (TDS). It was observed that the coagulation/filtration experiments were more efficient at removing turbidity, compared to the direct filtration process performed without any coagulation and filter media.

In this review, the main concept of ferroelectricity of perovskite oxides and related materials at nanometer scale and existing difficulties in the synthesis of those nanocrystals are discussed. Important effects, such as depolarization field and size effect, on the existence of ferroelectricity in perovskite nanocrystals are deliberated. In the discussion of modeling works, different theoretical calculations are pinpointed focusing on their studies of lattice dynamics, phase transitions, new origin of ferroelectricity in nanostructures, etc. As the major part of this review, recent research progress in the facile synthesis, characterization and various applications of perovskite ferroelectric nanomaterials, such as BaTiO₃, PbTiO₃, PbZrO₃, and BiFeO₃, are also scrutinized. Perspectives concerning the future direction of ferroelectric nanomaterials research and its potential applications in renewable energy, etc., are presented. This review provides an overview in this area and guidance for further studies in perovskite ferroelectric nanomaterials and their applications.

A synthetic method of using genetically engineered M13 virus to mineralize perovskite nanomaterials, particularly strontium titanate (STO) and bismuth ferrite (BFO), is presented. Genetically engineered viruses provide effective templates for perovskite nanomaterials. The virus-templated nanocrystals are small in size, highly crystalline, and show photocatalytic and photovoltaic properties., (Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Mechanically durable, long-lasting antifog coatings based on polysaccharides were developed using a layer-by-layer (LBL) assembly process. The unique properties of these coatings are a result of a molecular-level blending of the polysaccharides, with multilayers containing chitosan and carboxymethyl cellulose providing the best overall properties. The antifog properties resulted from a strong interaction between the polar and H-bonding elements of the assembled polymers and water molecules and the concomitant formation of thin films of water. Environmental scanning electron microscopy (ESEM) studies confirmed that fogging coatings are decorated with light scattering, micrometer-sized droplets of water whereas antifogging coatings remain droplet free. To improve the mechanical durability of the multilayer films on substrates, the surface was modified via self-assembly of epoxy-functionalized silane molecules. Cross-linking chemistry was then applied to improve the mechanical robustness of the LBL films on various surfaces. These films were characterized using several techniques: optical profilometery (PL), spectroscopic ellipsometry (EL), contact angle goniometry (CA), and atomic force microscopy (AFM). The antifog properties of the films were evaluated by several tests under different environmental conditions. This work demonstrates that the unique water-adsorbing properties of polysaccharides can be exploited to create permanent antifog properties, which may be useful for various applications.

Polystyrene (PS) and polyvinyl chloride (PVC) fibers incorporated into TiO(2) nanoparticles and graphene nanoflakes were fabricated by an electrospinning technique, and then the surface morphology and superhydrophobicity of these electrospun nanocomposite fibers were investigated. Results indicated that the water contact angle of the nanocomposite fiber surfaces increases to 178° on the basis of the fiber diameter, material type, nanoscale inclusion, heat treatment, and surface porosity/roughness. This is a result of the formation of the Cassie-Baxter state in the fibers via the nanoparticle decoration, bead formation, and surface energy of the nanofiber surface. Consequently, these superhydrophobic nanocomposite fibers can be utilized in designing photoelectrodes of dye-sensitized solar cells (DSSCs) as self-cleaning and anti-icing materials for the long-term efficiency of the cells.

From top to bottom: Peptide lines were formed in trenches in the self-assembled monolayer (SAM) on an Au substrate. Combination of the top-down (peptide nanolithography) and the bottom-up fabrications (biomineralization) yielded arrays of monodisperse Au nanoparticles assembled on the peptide lines (see picture). The number of nanoparticles on the lines was simply determined by the width of the peptide pattern.

Single crystalline nanoneedles of polyaniline (PANI) and polypyrrole (PPY) were synthesized using an interfacial polymerization for the first time. The interfacial crystallization of conductive polymers at the liquid/liquid interface allowed PANI and PPY polymers to form single crystalline nanocrystals in a rice-like shape in the dimensions of 63 nm x 12 nm for PANI and 70 nm x 20 nm for PPY. Those crystalline nanoneedles displayed a fast conductance switching in the time scale of milliseconds. An important growth condition necessary to yield highly crystalline conductive polymers was the extended crystallization time at the liquid/liquid interfaces to increase the degree of crystallization. As compared to other interfacial polymerization methods, lower concentrations of monomer and oxidant solutions were employed to further extend the crystallization time. While other interfacial growth of conducting polymers yielded noncrystalline polymer fibers, our interfacial method produced single crystalline nanocrystals of conductive polymers. We recently reported the liquid/liquid interfacial synthesis of conducting PEDOT nanocrystals; however, this liquid/liquid interfacial method needs to be extended to other conductive polymer nanocrystal syntheses in order to demonstrate that our technique could be applied as the general fabrication procedure for the single crystalline conducting polymer growth. In this report, we showed that the liquid/liquid interfacial crystallization could yield PANI nanocrystals and PPY nanocrystals, other important conductive polymers, in addition to PEDOT nanocrystals. The resulting crystalline polymers have a fast conductance switching time between the insulating and conducting states on the order of milliseconds. This technique will be useful to synthesize conducting polymers via oxidative coupling processes in a single crystal state, which is extremely difficult to achieve by other synthetic methods.

Previously, a large scale assembly of nanowires in a parallel array configuration has been demonstrated, and one type of nanowire could interconnect two electrodes in the high-wire density. However, to assemble nanowires into practical logic-gate configurations in integrated circuits, we need more than the parallel assembly of nanowires. For example, when the assembling nanowires are monopolar semiconductors, logic gates such as AND, OR and NOR are to be assembled necessarily from two types of semiconducting nanowires, n-type and p-type, and some of these nanowires must cross perpendicularly to form a crossbar geometry for the logical operation. In this paper, the crossbar assembly of antibody-functionalized peptide nanotubes was demonstrated by a new biomimetic bottom-up technique. Molecular recognition between antigens and antibodies enabled two types of the antibody-functionalized bionanotubes to place them onto targeted locations on substrates, where their complementary antigens were patterned. When two rectangular pads of antigens, human IgG and mouse IgG, were patterned perpendicularly on an Au substrate by nanolithography and then the antihuman IgG nanotubes and the antimouse IgG nanotubes were incubated on this substrate in solution, these bionanotubes were attached onto corresponding locations to form the crossbar configuration.

Capacitances of five types of viruses, adenovirus type 5 (AV5), herpes simplex virus type 1 (HSV1), simian virus 40 (SV40), vaccinia (MVA), and cowpea mosaic virus (CPMV), were compared by AC capacitance scanning probe microscopy. This technique, using a Pt-coated AFM tip as an electrode to probe capacitance of materials between the tip and a bottom electrode, has been applied to study surface structures of semiconductors and polymers with nanometer spatial resolution; however, biological samples at the nanoscale have not been explored by this technique yet. Because most biological cells are poor conductors, this approach to probe electric properties of cells by capacitance is logical. This scanning probe technique showed that each virus has distinguishable and characteristic capacitance. A series of control experiments were carried out using mutant viruses to validate the origin of the characteristic capacitance responses for different viruses. A mutation on the capsid in HSV1 with green fluorescence proteins increased capacitance from 9 x 10(-6) to 1 x 10(-5) F/cm2 at the frequency of 10(4) Hz. Herpes simplex virus type 2 (HSV2) decreased capacitance when its envelope and glycoproteins were chemically extracted. These control experiments indicate that dielectric properties of capsid proteins and envelope glycoproteins significantly influence overall dielectric constants of viruses. Because those capsid proteins and glycoproteins are characteristic of the virus strain, this technique could be applied to detect and identify viruses at the single viron level using their distinct capacitance spectra as fingerprints without labeling.

In this letter, we report the first facile open-bench synthesis of BaTiO3, SrTiO3 nanocrystals, and their nanosolid solutions BaxSr1-xTiO3 (BST) at 80 degrees C. The size of the BST nanoparticles was readily tuned from approximately 50 to approximately 10 nm with achievable giant dielectric constants. The process yielded these important perovskite mixed-metal oxide crystals of high quality on the nanometer scale without a history of thermal stress. This new synthesis system involves inorganic starting materials without organic components and does not require demanding conditions such as an inert environment, high pressure, and high temperature.

The shape of silica nanoparticles is controlled when they are synthesized at liquid/liquid interfaces; the combination of organic and aqueous phases that form the interface can change the shape of silica into a triangle, cube, or rod.

The peptide nano-rings containing Au nanoparticles inside their cavities were self-assembled on dithiol SAMs patterned as an array by AFM-based nanolithography. The peptide nano-rings were aligned as a line on these SAMs, and Au formed lines with the spacing between these nanoparticles as the peptide nano-rings functioned as spacers. This type of array fabrication will provide improved tunability in their optical properties of resulting nanoparticle-assembled arrays. In addition, optimization of the inter-particle distance of nanoparticles in the array with various spacers may allow one to design new types of photonic crystals with desired optical properties.

Application of biotechnology in nanofabrication has an advantage to produce functional building-block materials that may not have synthetic counterparts. Here we introduced a new type of building block, antibody nanotubes, and demonstrated anchoring them on complementary antigen arrays via antibody-antigen recognition. Biological recognition between the antibody nanotubes and the antigen arrays permitted recognition-driven assembly of ordered nanotube arrays. The array of antigens was written by using the tip of an atomic force microscope (AFM) on alkylthiol self-assembled monolayer (SAM)-coated Au substrates via nanografting. After antigens were immobilized onto the shaved regions of the alkylthiol SAMs with the AFM tip, antibody nanotubes, produced by incubating antibodies in template nanotube solutions, were selectively attached onto the antigen regions. This technique is very useful when multiple building blocks are necessary to address specific locations on substrates because simultaneous immobilization of multiple antibody nanotubes at specific complementary binding positions can be achieved in a single process.