New Epoxy and Hardener System Based on an Imidazolium Ionic Liquid as an Anticorrosive Coating for Steel in the Marine Environment.

The large sizes of cations and anions of organic salts are the driving force for the application of ionic liquids (organic salts) in harsh salty conditions. Moreover, the formation of crosslinked ionic liquid networks as anti-rust and anticorrosion protective films on the substrate surfaces repels seawater salt and water vapor from their surface to prevent corrosion. In this respect, an imidazolium epoxy resin and polyamine hardener as ionic liquids were prepared by the condensation of either pentaethylenehexamine or ethanolamine with glyoxal and p-hydroxybenzaldehyde or formalin in acetic acid as a catalyst. The hydroxyl and phenol groups of the imidazolium ionic liquid were reacted with epichlorohydrine in the presence of NaOH as a catalyst to prepare polyfunctional epoxy resins. The chemical structure, nitrogen content, amine value, epoxy equivalent weight, thermal characteristics, and stability of the imidazolium epoxy resin and polyamine hardener were evaluated. Moreover, their curing and thermomechanical properties were investigated to confirm the formation of homogeneous, elastic, and thermally stable cured epoxy networks. The corrosion inhibition and salt spray resistance of the uncured and cured imidazolium epoxy resin and polyamine as coatings for steel in seawater were evaluated.

Enhanced Delivery of Insulin through Acrylamide-Modified Chitosan Containing Smart Carrier System.

The present study develops on insulin-release studies from the chitosan-amide-modified stimuli-responsive polymers formed from various fatty acids including stearic acid, oleic acid, linoleic acid, and linolenic acid. This is the continuation of an earlier reported study that investigates the insulin-release profiles of chitosan-modified fatty acid amides (without stimuli responsive polymers). Following the synthesis and characterization of many different fatty acid amides with a varying amount of unsaturation, the insulin drug loading and release effects were compared among N-isopropylacrylamide (NIPAm), a thermo-responsive polymer, and 2-acrylamide-2-methylpropane sulfonic acid (AMPS), a pH-responsive polymer-modified hydrogel that is expected to enhance environmental response and the controllability of release. Finally, drug release effects were studied to investigate the drug release mechanisms with the help of five different pharmacokinetic models including the zero-order, first-order, Higuchi, Korsmeyers-Peppas, and Hixson models. The results indicate that the Higuchi and Hixson models are valid in terms of the operation of the NIPAm and AMPS matrices during the delivery of insulin.

New Amphiphilic Ionic Liquids for the Demulsification of Water-in-Heavy Crude Oil Emulsion.

This work aimed to use abietic acid (AA), as a widely available natural product, as a precursor for the synthesis of two new amphiphilic ionic liquids (AILs) and apply them as effective demulsifiers for water-in-crude oil (W/O) emulsions. AA was esterified using tetraethylene glycol (TEG) in the presence of p-toluene sulfonic acid (PTSA) as a catalyst obtaining the corresponding ester (AATG). AATG was reacted with 1-vinylimidazole (VIM) throughout the Diels-Alder reaction, forming the corresponding adduct (ATI). Following this, ATI was quaternized using alkyl iodides, ethyl iodide (EI), and hexyl iodide (HI) to obtain the corresponding AILs, ATEI-IL, and ATHI-IL, respectively. The chemical structure, surface activity, thermal stability, and relative solubility number (RSN) were investigated using different techniques. The efficiency of ATEI-IL and ATHI-IL to demulsify W/O emulsions in different crude oil: brine volumetric ratios were evaluated. ATEI-IL and ATHI-IL achieved promising results as demulsifiers. Their demulsification efficiency increased as the brine ratios decreased where their efficiency reached 100% at the crude oil: brine ratio (90:10), even at low concentrations.

Application of Silica Nanoparticles for Improving Growth, Yield, and Enzymatic Antioxidant for the Hybrid Rice EHR1 Growing under Water Regime Conditions.

The current study was designed to assess the effect of different concentrations of silica oxide nanoparticles (SiO2NPs) (0, 30, 60, and 90 ppm) as foliar applications under three irrigation regimes i.e., irrigation every 3 days (IR3, control), irrigation every 6 days (IR6), and irrigation every 9 days (IR9) on growth, yield and certain metabolites of rice (Oryza sativa L. cv. EHR1). To achieve such a goal, 2 field experiments were conducted during the 2018 and 2019 seasons at the Experimental Farm of Rice Research and Training Center (RRTC), Sakha Agricultural Station, Kafr El-sheik, Egypt. Firstly, the as-prepared nanoparticles of SiO2 were prepared from useless materials (RHs) which are considered as one of the bio burdens on the environment via treating with HCl and followed by drying and calcination. Consequently, the synthesis was examined by making use of advanced tools such as X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS) for illustrating the hydrodynamic particle size of SiO2NPs and scanning electron microscopy (SEM). The nanoparticles were formed with nearly spherical shape and small size. The results indicated that leaf area index, dry matter production, the number of panicles/m2, the number of filled grains/ panicles, 1000 grain weight, grain yield, and biological yield as well as chlorophyll content have witnessed a significant increase under irrigated application every 3 and 6 days. Whilst a prolonged irrigation regime up to 9 days recorded a remarkable decline in the aforementioned characteristics except for the number of unfilled grains/panicle which increased considerably in both seasons. On the other hand, proline concentration and the activity of the antioxidant enzymes were increased in both irrigated treatments every 6 and 9 days compared with control treatment (irrigation every 3 days). The foliar supplementations of (SiO2NPs) contributed to ameliorating all the aforementioned characteristics progressively up to the dosage of 90 ppm compared to control treatment (no Si/NPS application) in both seasons. Invariably, growth and yield parameters in water-stressed plants treated with SiO2NPs were higher than those in water-stressed plants without SiO2NPs addition. Based on that, it could be concluded that the foliar application of SiO2NPs can mitigate the adverse effect of water stress on rice plants.

Nd(III) and Gd(III) Sorption on Mesoporous Amine-Functionalized Polymer/SiO2 Composite.

The strong demand for rare-earth elements (REEs) is driven by their wide use in high-tech devices. New processes have to be developed for valorizing low-grade ores or alternative metal sources (such as wastes and spent materials). The present work contributed to the development of new sorbents for the recovery of rare earth ions from aqueous solutions. Functionalized mesoporous silica composite was synthesized by grafting diethylenetriamine onto composite support. The physical and chemical properties of the new sorbent are characterized using BET, TGA, elemental analysis, titration, FTIR, and XPS spectroscopies to identify the reactive groups (amine groups: 3.25 mmol N g-1 and 3.41 by EA and titration, respectively) and their mode of interaction with Nd(III) and Gd(III). The sorption capacity at the optimum pH (i.e., 4) reaches 0.9 mmol Nd g-1 and 1 mmol Gd g-1. Uptake kinetics are modeled by the pseudo-first-order rate equation (equilibrium time: 30-40 min). At pH close to 4-5, the sorbent shows high selectivity for rare-earth elements against alkali-earth elements. This selectivity is confirmed by the efficient recovery of REEs from acidic leachates of gibbsite ore. After elution (using 0.5 M HCl solutions), selective precipitation (using oxalate solutions), and calcination, pure rare earth oxides were obtained. The sorbent shows promising perspective due to its high and fast sorption properties for REEs, good recycling, and high selectivity.

New Amphiphilic Tricationic Imidazolium and Pyridinium Ionic Liquids for Demulsification of Arabic Heavy Crude Oil Brine Emulsions.

Preparation of new green oilfield chemicals based on ionic liquids (ILs) having higher demulsification efficiency to solve the heavy crude oil brine water emulsions became a target in the petroleum research studies and industry. In the present work, the combination of pyridinium, imidazolium, and hydrophilic or hydrophobic moieties in the chemical structure of ILs has been investigated to improve the surface properties of ILs in both bulk solution and interfaces. Aminopyridine was quaternized with cetylbromide and condensed with glyoxal and 4-hydroxybenzaldehyde in acetic acid to prepare imidazolium-pyridinium bromide acetate ionic liquid (IPy-IL). The phenol group of IPy-IL was etherified with tetraethylene glycol to alter its amphiphilicity and synthesize new amphiphiles (AIPy-IL). Their chemical structure, thermal characteristics, and stabilities were characterized. Their aqueous solution performance in seawater was evaluated to investigate their surface activity, aggregation particle sizes, and surface charges. The demulsification performances of the prepared Arabic heavy crude oil seawater emulsions in the presence of different concentrations of IPy-IL and AIPy-IL were evaluated and proved by interfacial tension, particle size, and demulsification efficiencies at a temperature of 45 °C. The data concluded that AIPy-IL was an effective demulsifier for different crude oil seawater emulsion compositions at a low injection dose and temperature of 100 ppm and 45 °C, which were not report elsewhere.

Immobilization of silver and strontium oxide aluminate nanoparticles integrated into plasma-activated cotton fabric: luminescence, superhydrophobicity, and antimicrobial activity.

Smart textiles with a multifunctional surface, such as with photoluminescence, antimicrobial, and superhydrophobic properties, are highly desirable. Silver nanoparticles (Ag NPs) were prepared and immobilized onto a cotton surface using a facile pad-dry-curing technique to introduce long-lasting antimicrobial properties. The morphology of the silver immobilized cotton fibres was explored using scanning electron microscopic images and energy-dispersive X-ray spectra. The morphology of the formed Ag NPs was determined using a transmission electron microscope. Ag NPs exhibited uniform spreading and a high deposition density with a particle diameter in the range 25-55 nm. Both photoluminescence and superhydrophobic properties were explored by studying the cotton samples treated with hexadecyltrimethoxysilane nanocomposite containing lanthanide-doped strontium oxide aluminate NPs. Ultraviolet-visible light absorption, phosphorescence, and lifetime spectra were measured. The produced transparent superhydrophobic and photoluminescent film showed two absorbance bands at 273 and 367 nm and emission bands at 415 and 437 nm, as recognized by both absorption and emission spectra. Excellent antibacterial activities towards E. coli and S. aureus were monitored for the coated samples. Both fastness and colorimetric properties of Ag NPs-coated fabrics were explored.

Green Synthesis of Zinc Oxide Nanoparticles: Fortification for Rice Grain Yield and Nutrients Uptake Enhancement.

Applications of metal oxide nanoparticles in the agriculture sector are being extensively included as the materials are considered superior. In the present work, zinc oxide nanoparticle (ZnO NPs), with a developing fertilizer, is applied in the fortification of rice grain yield and nutrient uptake enhancement. To evaluate the role of ZnO NP, two field experiments were conducted during the 2018 and 2019 seasons. ZnO NPs were small, nearly spherical, and their sizes equal to 31.4 nm, as proved via the dynamic light scattering technique. ZnO NPs were applied as a fertilizer in different concentrations, varying between 20 and 60 mg/L as a foliar spray. The mixture of ZnSO4 and ZnO NP40 ameliorated yield component and nutrients (N, K, and Zn) uptake was enhanced compared to traditional ZnSO4 treatment. Nevertheless, the uptake of the phosphorous element (P) was adversely affected by the treatment of ZnO NPs. Thus, treatment via utilizing ZnO NPs as a foliar with a very small amount (40 ppm) with of basal ZnSO4 led to a good improvement in agronomic and physiological features; eventually, higher yield and nutrient-enriched rice grain were obtained.

Fabrication of New Demulsifiers Employing the Waste Polyethylene Terephthalate and their Demulsification Efficiency for Heavy Crude Oil Emulsions.

Two novel amphiphilic polyethylene amine terephthalate have been prepared via the glycolsis of polyethylene terephthalate (PET). The product, bis (2-hydroxyethyl terephthalate) (BHET), was converted to the corresponding dialkyl halide, bis(2-chloroethyl) terephthalate (BCET), using thionyl chloride (TC). This dialkyl compound was used for alkylation of dodecyl amine (DOA) and tetraethylenepentamine (TEPA) or pentaethylenehexamine (PEHA) to form the corresponding polyethylene amine terephthalate, i.e., DOAT and DOAP, respectively. Their chemical structure, surface tension, interfacial tension (IFT), and dynamic light scattering (DLS) were determined using different techniques. The efficiency of the prepared polyethylene amine terephthalate to demulsify water in heavy crude (W/O) emulsions was also determined and found to increase as their concentrations increased. Moreover, DOAT showed faster and higher efficiency, and cleaner separation than DOAP.

Seawater Absorption and Adhesion Properties of Hydrophobic and Superhydrophobic Thermoset Epoxy Nanocomposite Coatings.

The enhancement of both thermal and mechanical properties of epoxy materials using nanomaterials becomes a target in coating of the steel to protect it from aggressive environmental conditions for a long time, with reducing the cost. In this respect, the adhesion properties of the epoxy with the steel surfaces, and its proper superhyrophobicity to repel the seawater humidity, can be optimized via addition of green nanoparticles (NPs). In-situ modification of silver (Ag) and calcium carbonate (CaCO3) NPs with oleic acid (OA) was carried out during the formation of Ag-OA and CaCO3-OA, respectively. The epoxide oleic acid (EOA) was also used as capping for Ca-O3 NPs by in-situ method and epoxidation of Ag-OA NPs, too. The morphology, thermal stability, and the diameters of NPs, as well as their dispersion in organic solvent, were investigated. The effects of the prepared NPs on the exothermic curing of the epoxy resins in the presence of polyamines, flexibility or rigidity of epoxy coatings, wettability, and coatings durability in aggressive seawater environment were studied. The obtained results confirmed that the proper superhyrophobicity, coating adhesion, and thermal stability of the epoxy were improved after exposure to salt spray fog for 2000 h at 36 °C.

Magnetic Ionic Liquid Nanocatalyst to Improve Mechanical and Thermal Properties of Epoxy Nanocomposites.

New magnetic imidazolium ionic liquid (IIL) was synthesized to improve the curing, mechanical, and thermal characteristics of the epoxy/polyamine system. In this respect, 2-(4-minophenyl)-1.3-bis(triethoxysilyl)-1H-imidazol-3-ium acetate as IIL was synthesized and characterized by different spectroscopy tools. The IIL was used as capping to prepare Fe3O4 nanoparticles (NPs) as new Fe3O4-IIL NPs. The thermal stability, morphology, crystal lattice structures, and magnetic properties were evaluated to confirm the formation of uniform, thermal, stable, and superparamagnetic Fe3O4-IIL NPs. The prepared Fe3O4-IIL NPs were mixed with an epoxy/polyamine system to improve the curing, thermal, and mechanical properties of epoxy through chemical reactions. The dynamic mechanical analyzer and differential scanning calorimeter were used to investigate the flexibility and storage modulus of the cured epoxy/polyamine system in the absence and presence of Fe3O4-IIL NPs. The atomic force microscope and scanning electron microscope were used to evaluate the dispersion and embedding of Fe3O4-IIL NPs into epoxy matrix. The thermal, mechanical, and surface morphologies data confirmed that the incorporation of Fe3O4-IIL NPs using 3 wt. % during the curing of an epoxy/polyamine system produces superior epoxy films without cracks, holes, and NPs agglomeration.

Antibacterial and Anti-Fungal Biological Activities for Acrylonitrile, Acrylamide and 2-Acrylamido-2-Methylpropane Sulphonic Acid Crosslinked Terpolymers.

There is a pressing demand to synthesize polymers that have antibacterial and antifungal properties. The aim of this study was to synthesize a crosslinked hydrophilic terpolymer with acrylamide, acrylonitrile, acrylic acid, acrylamido-2-methylpropane sulphonic acid and ethylene glycol dimethacrylate as a crosslinker. The chemical structure and thermal stability of the prepared cross-linked terpolymers were confirmed by spectroscopic and thermal analyses. Moreover, the swelling experiments were performed to investigate their swelling capacity. Furthermore, the efficiency of the synthesized cross-linked polymer gels was assessed as an antimicrobial agent against Gram-positive, Gram-negative bacteria and fungal strains. The synthesized polymers showed broad inhibition effect, with more antibacterial activity by the AM4 polymer sample containing high percentage of acrylonitrile monomer in the prepared terpolymers (4 mol ratio of acrylic acid: 1 mol ratio of acrylamide: 16 mole ratio of acrylonitrile against Gram negative bacterial strain), while sample M3 terpolymer (1 mol ratio of acrylamide: 1 mole ratio acrylonitrile: 3 mole ratio of acrylamido-2-methylpropane sulphonic acid) showed a promising anti-fungal activity.

Synthesis and Application of New Amphiphilic Asphaltene Ionic Liquid Polymers to Demulsify Arabic Heavy Petroleum Crude Oil Emulsions.

Asphaltenes are heavy petroleum crude oil components which limit the production of petroleum crude oil due to their aggregation and their stabilization for all petroleum crude oil water emulsions. The present study aimed to modify the chemical structures of isolated asphaltenes by converting them into amphiphilic polymers containing ionic liquid moieties (PILs) to demulsify the emulsion and replace the asphaltene layers surrounding the oil or water droplets in petroleum crude oil emulsions. The literature survey indicated that no modification occurred to produce the PILs from the asphaltenes. In this respect, the asphaltenes were modified via oxidation of the lower aliphatic chain through carboxylation followed by conversion to asphaltene acid chloride that reacted with ethoxylated N-alkyl pyridinium derivatives. Moreover, the carboxylation of asphaltenes was carried out through the Diels-Alder reaction with maleic anhydride that was linked with ethoxylated N-alkyl pyridinium derivatives to produce amphiphilic asphaltene PILs. The produced PILs from asphaltenes acid chloride and maleic anhydride were designated as AIL and AIL-2. The chemical structure and thermal stability of the polymeric asphaltene ionic liquids were evaluated. The modified structure of asphaltenes AIL and AIL-2 exhibited different thermal characteristics involving glass transition temperatures (Tg) at -68 °C and -45 °C, respectively. The new asphaltenes ionic liquids were adsorbed at the asphaltenes surfaces to demulsify the heavy petroleum crude emulsions. The demulsification data indicated that the mixing of AIL and AIL-2 100 at different ratios with ethoxylated N-alkyl pyridinium were demulsified with 100% of the water from different compositions of O:W emulsions 50:50, 90:10, and 10:90. The demulsification times for the 50:50, 90:10, and 10:90 O:W emulsions were 120, 120, and 60 min, respectively. The interaction of the PILs with asphaltene and mechanism of demulsification was also investigated.

One-Step Synthesis of Amphiphilic Nonylphenol Polyethyleneimine for Demulsification of Water in Heavy Crude Oil Emulsions.

The demulsification of water-in-heavy crude oil emulsion with water droplet size in the microscale has drawn great attention because of their high stability and difficulty of separation. In the present work, a series of ethylene amine-based demulsifiers were prepared in one step through the interaction of pentaethylene hexamine, tetraethylene pentamine, and triethylene tetramene with glycidyl 4-nonylphenyl ether. The amphiphilic polyethyleneimine (APEI) abbreviated as DNPA-6, DNPA-5, and DNPA-4 were prepared to adjust their hydrophile-lipophile balances (HLB) to meet the requirement of the demulsification. 1HNMR, 13CNMR, and FTIR spectra were utilized to verify their chemical structures. The surface properties and zeta potential were also investigated. Demulsifier dose, separation time, and HLB values were taken into account to evaluate the demulsification efficiency of the synthesized APEI. The results suggested that the prepared demulsifiers had high ability to reduce the surface and interfacial tensions and also broke successfully water-in-Arabian heavy crude oil emulsions. The demulsification efficiency of DNPA-5 reached 100% for crude oil/water emulsion (90/10 vol %).

Green Technology for Remediation of Water Polluted with Petroleum Crude Oil: Using of Eichhornia crassipes (Mart.) Solms Combined with Magnetic Nanoparticles Capped with Myrrh Resources of Saudi Arabia.

Crude oil pollution of water bodies is a worldwide problem that affects water ecosystems and is detrimental to human health and the diversity of living organisms. The objective of this study was to assess the ability of water hyacinth (Eichhornia crassipes (Mart.) Solms) combined with the presence of magnetic nanoparticles capped with natural products based on Myrrh to treat fresh water contaminated by crude petroleum oil. Magnetic nanoparticles based on magnetite capped with Myrrh extracts were prepared, characterized, and used to adsorb heavy components of the crude oil. The hydrophobic hexane and ether Myrrh extracts were isolated and used as capping for magnetite nanoparticles. The chemical structures, morphologies, particle sizes, and magnetic characteristics of the magnetic nanoparticles were investigated. The adsorption efficiencies of the magnetic nanoparticles show a greater efficiency to adsorb more than 95% of the heavy crude oil components. Offsets of Water hyacinth were raised in bowls containing Nile River fresh water under open greenhouse conditions, and subjected to varying crude oil contamination treatments of 0.5, 1, 2, 3, and 5 mL/L for one month. Plants were harvested and separated into shoots and roots, oven dried at 65 °C, and grounded into powder for further analysis of sulphur and total aromatic and saturated hydrocarbons, as well as individual aromatic constituents. The pigments of chlorophylls and carotenoids were measured spectrophotometrically in fresh plant leaves. The results indicated that the bioaccumulation of sulphur in plant tissues increased with the increased level of oil contamination. Water analysis showed significant reduction in polyaromatic hydrocarbons. The increase of crude oil contamination resulted in a decrease of chlorophylls and carotenoid content of the plant tissues. The results indicate that the water hyacinth can be used for remediation of water slightly polluted by crude petroleum oil. The presence of magnetite nanoparticles capped with Myrrh resources improved the remediation of water highly polluted by petroleum crude oil.

Novel Superadsorbent Highly Porous Hydrogel Based on Arabic Gum and Acrylamide Grafts for Fast and Efficient Methylene Blue Removal.

Environmental pollution with dyes released from industrial effluent is one of the major and most critical problems in the world. To alleviate this issue, advanced and safe materials with fast and highly efficient dye removal should be designed. Great attention has been paid recently to hydrogels based on polysaccharides such as Arabic Gum (AG) grafted with polyacrylamide (PAM) and polyacrylic acid (PAA). These materials combine the merits of natural polymers such as biodegradability and non-toxicity with the high adsorption ability of PAM and PAA towards cationic dyes such as methylene blue (MB). Many previous works have been done to enhance three-dimensional (3D) structure and swelling ability of the graft copolymers by using a crosslinking agent or even adding nanomaterials as a filler inside the hydrogel matrix. However, these additives may negatively affect the adsorption ability, and few previous studies could reach 2000 mg/g of maximum MB capacity removal within a good period of time. In our work, we synthesized partially hydrolyzed polyacrylamide grafted Arabic gum (AG-g-PAM/PAA) to have both amide and carboxylate groups. The modified water dissolved graft product undergoes water in oil (W/O) emulsion using paraffin oil as the continuous phase and Triton X-100 as a stabilizing agent; then, the system was inversed to oil in water (O/W) emulsion by increasing the shear mixing rate and cross-linked using Epichlorohydrin (ECH). The precipitated graft product showed hierarchically interconnected micro and macropores' sponge like shape with fast water swelling and high MB adsorption capacity (2300 mg g-1) after 45 min at near neutral pH conditions.

Methylene Blue Catalytic Degradation Using Silver and Magnetite Nanoparticles Functionalized with a Poly(ionic liquid) Based on Quaternized Dialkylethanolamine with 2-Acrylamido-2-methylpropane Sulfonate-co-Vinylpyrrolidone.

Catalytic degradation of organic water pollutants has emerged as a cost- and energy-effective technique to treat wastewater. In this work, new silver and magnetite nanoparticles (NPs) were prepared with a protic poly(ionic liquid) (PIL) based on a quaternized diethylethanolamine cation combined with 2-acrylamido-2-methylpropane sulfonate-co-vinylpyrrolidone (QAMPSA/VP) as a capping and a reducing agent. The morphology, particle size, surface charge, thermal stability, and magnetic properties of QAMPS/VP-Ag and Fe3O4 NPs were investigated to determine the efficiency of the PIL as a reducing and a capping agent to protect the produced NPs from oxidation or thermal degradation. The activation energy, enthalpy, and entropy of the catalytic degradation of the cationic methylene blue (MB) dye in the presence of QAMPS/VP-Ag and Fe3O4 NPs were determined. The data elucidated that MB was completely degraded in 8 min in the presence of QAMPS/VP-Fe3O4 NPs as a Fenton oxidation catalyst. Moreover, their good magnetic properties allowed their easy separation and reuse for five cycles without losing their magnetic or catalytic properties.

Reactive Mesoporous pH-Sensitive Amino-Functionalized Silica Nanoparticles for Efficient Removal of Coomassie Blue Dye.

In this work, new smart mesoporous amine-functionalized silica nanoparticles were prepared from hydrolyzing microgels based on N-isopropyl acrylamide-co-vinyltrimethoxysilane microgels with tetraethoxysilicate and 3-aminopropyltriethoxysilane by sol-gel method. The thermal stability and Fourier transform infrared were used to determine the amine contents of the silica nanoparticles. The pH sensitivity of the synthesized silica nanoparticles in their aqueous solutions was evaluated by using dynamic light scattering (DLS) and zeta potential measurements. The porosity of the amine-functionalized silica nanoparticles was evaluated from a transmittance electron microscope and Brunauer-Emmett-Teller (BET) plot. The results have positively recommended the pH-sensitive amine-functionalized silica nanoparticles as one of the effective nano-adsorbent to remove 313 mg·g-1 of CB-R250 water pollutant.

Preparation of pH Responsive Polystyrene and Polyvinyl Pyridine Nanospheres Stabilized by Mickering Microgel Emulsions.

New pH-sensitive polystyrene, PS, and poly(4-vinylpyridine), P4-VP, nanospheres were prepared by using surfactant-free method based on soft microgels (Mickering emulsion). The formation of stable Mickering cyclohexane/water emulsions was investigated by using soft microgel particles of poly(acrylamide), PAAm, poly(2-acrylamido-2-methylpropane sulfonic acid), PAMPS, and sodium salt of PAMPS, PAMPS-Na, as stabilizers. The dynamic light scattering (DLS), optical microscopy, and scanning electron microscopy (SEM) were used to investigate the optimum conditions and effects of surrounding solutions on the microgels characteristics and their corresponding Mickering emulsions. The cyclohexane/water Mickering emulsions stabilized by softer and neutral charged microgels were considerably more stable under the same conditions. Furthermore, the stimuli-responsive properties of PAMPS microgel stabilized cyclohexane/water Mickering emulsions suggest the potential utility in the preparation of PS and P4-VP nanospheres. The effects of pH changes on the morphology, particle sizes, and surface charges of PS and P4-VP microgels were evaluated to prove the pH-sensitivity of the prepared nanospheres.

New Smart Magnetic Ionic Liquid Nanocomposites Based on Chemically Bonded Imidazole Silica for Water Treatment.

New magnetic silica imidazolium ionic liquid nanocomposites were synthesized by a sol-gel technique. The (3-aminopropyl)triethoxysilane (APTS) was condensed with glyoxal and p-hydroxybenzaldehyde in acetic acid to produce an amino-modified silica ionic liquid (Si-IIL). The APTS was condensed with TEOS in ethanol and water to prepare amino-modified SiO2 nanoparticles. The produced amino-modified SiO2 silica was condensed with glyoxal and p-hydroxybenzaldehyde in acetic acid to produce chemically bonded silica SiO2-IIL. The SiO2-IIL and Si-IIL were used as capping agents during and after the formation of magnetite nanoparticles in ammonia to produce magnetic SiO2-IIL-Fe3O4 and Fe3O4-Si-IIL adsorbents, respectively. Their chemical structure, morphology, crystalline lattice structure, surface charges, particle sizes, and magnetic characteristics elucidated the formation of core-shell and highly dispersed magnetic nanocomposites. The saturation magnetization values of Fe3O4-Si-IIL and SiO2-IIL-Fe3O4 were 35.3 and 30.8, respectively. The uniform dispersed disconnected spherical morphologies appeared for Fe3O4-Si-IIL hybrid and the core-shell spherical morphology obtained with SiO2-IIL-Fe3O4 hybrid NPs. The Fe3O4-Si-IIL and SiO2-IIL-Fe3O4 show an excellent high chemical adsorption capacities as 460.3 and 300.9 mg·g-1, respectively (not reported in the literature) when used as an adsorbent to remove CB-R250 water pollutant under optimum conditions. Their applicability and reusability as fast and highly effective adsorbents for Coomassie blue (CB-R250) organic water pollutants were investigated.