Viscosity of aqueous ionic liquids analogues as a function of water content and temperature

Ionic liquids analogues known as Deep Eutectic Solvents (DESs) are gaining a surge of interest by the scientific community, and many applications involving DESs have been realized.Moisture content is one of the important factors that affects the physical and chemical characteristics of these fluids. In this work, the effect of mixing water with three common type Ⅲ DESs on their viscosity was investigated within the water mol fraction range of (0-1) and at the temperature range (298.15-353.15 K). Similar trends of viscosity variation with respect to molar composition and temperature were observed for the three studied systems. Due to the asymmetric geometry of the constituting molecules in these fluids, their viscosity could not be modeled effectively by the conventional Grunberg and Nissan model, and the Fang-He model was used to address this issue with excellent performance. All studied aqueous DES mixtures showed negative deviation in viscosity as compared to ideal mixtures. The degree of intermolecular interactions with water reaches a maximum at a composition of 30% aqueous DES solution. Reline, the most studied DES in the literature, showed the highest deviation. The information presented in thiswork on the viscosity of aqueous DES solutionsmay serve in tuning this important property for diverse industrial applications involving these novel fluids in fluid flow, chemical reactions, liquid-liquid separation and many more.     

Enzymatic Synthesis of <Emphasis Type="Italic">trans</Emphasis>-Free Structured Margarine Fat Analogues Using Stearidonic Acid Soybean and High Stearate Soybean Oils

Enzymatic synthesis of trans-free structured margarine fat analogues from stearidonic acid (SDA) soybean oil and high stearate soybean oil was optimized using response surface methodology. The independent variables considered were the substrate molar ratio (2–5), temperature (50–65 °C), time (6–22 h), and enzymes (Lipozyme^® TLIM and Novozym^® 435). The dependent variables were mol% stearic acid incorporation and mol% SDA content. A good-fit model was constructed using regression analysis with backward elimination and verified by a Chi-square test. Desirable and optimal products composition were achieved at 50 °C, 18 h, 2:1, using Lipozyme TLIM, with 15.6 mol% stearic acid and 9.2 mol% SDA in the product and at 58 °C, 14 h, 2:1, using Novozym 435, with 14.8 mol% stearic acid and 6.4 mol% SDA. Using optimal conditions, structured lipids (SL) were synthesized in a 1 L stir-batch reactor and free fatty acids removed by short-path distillation. SL were characterized for their fatty acid profile, sn-2 positional fatty acids, triacylglycerol profile, polymorphism, thermal behavior, and solid fat content. The SL had a desirable fatty acid profile, physical properties, and a suitable β′ polymorph content. These SL could be used as margarine fat analogues and an alternative to partially hydrogenated fat.     

High‐performance soluble copolyarylate based on phenolphthalein: synthesis,characterization and properties

A series of copolyarylates (PP0–PP100) containing phthalide groups was synthesized via interfacial polymerization from a mixture of phenolphthalein (PP) and bisphenol A with molar equivalent of terephthalyl chloride. Incorporating PP into the polymer chain improved the solubility of the polyarylates in common organic solvents. The glass transition temperature (191–314 °C), residual weight percentage, Young's modulus (1.7–2.8 GPa), solubility and complex melt viscosity of the copolyarylates increased with increasing PP units in the copolymerization. By contrast, crystallinity and elongation at break (14.1 to 11.2%) of the copolyarylates decreased with increasing PP units in the polymer backbone. When the PP content increased over 30 mol% (PP30), the copolyarylates became amorphous polymers. When the PP content was below 30 mol%, the copolyarylates exhibited good melt processability. With regards to its solubility, thermal stability, mechanical properties and melt processability, PP30 may be considered as a promising candidate in the field of processable high‐performance engineering plastics. © 2019 Society of Chemical Industry     

Electrospinning and thermal treatment of yttria doped zirconia fibres

As compared to a bulk material, the fibres exhibit novel physical and chemical properties arising from their unique geometric features such as high surface area, surface to volume ratio and small fibre diameter. This paper is focused on the fabrication of nanosized 8 mol% yttria doped zirconia fibres by electrospinning from propoxide/polyvinylpyrrolidonebased precursors and physical-chemical characterization of the ceramic fibres with an energy application potential. Fully crystalline composition of cubic zirconia was detected after fibre heat treatment at 700 °C. The fibre morphology was changed with increasing temperature from flexible nonsintered nanoparticle system at 700 °C through porous nanograin structure at 900 °C and nonporous structure with coarser nanograins at 1100 °C to fragile chain-like fibre structure formed of elongated submicrometer grains at 1300–1450 °C. The densification and grain growth kinetics were described in two stages in the temperature range from 700 °C up to 1450 °C.     

The effect of formaldehyde/phenol (F/P) molar ratios on function and curing kinetics of high‐solid resol phenolic resins

A series of high‐solid resol phenolic resins (HSRPRs) were synthesized with different molar ratios (1.6, 1.8, 2.0, 2.2, and 2.4) of formaldehyde to phenol using calcium oxide and sodium hydroxide as catalyst. The effects of F/P molar ratios on physical properties, free formaldehyde and phenol, activity, structure, and thermally resistant properties of HSRPRs were fully investigated by chemical assays, liquid and solid ¹³C‐NMR, Fourier transform infrared spectroscopy, and thermogravimetric analysis. The curing kinetics of different F/P molar ratios were explored with differential scanning calorimeter at four different heating rates (5, 10, 15, 20°C/min) from 35 to 200°C. Overall, HSRPRs with F/P = 2.0 had excellent comprehensive properties. The study was significant in solving the wastewater problem during the process of industry‐scale preparation of HSRPRs. We believed that the experimental findings would provide a new avenue for further study and application of HSRPRs. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Effects of curing accelerators on physical properties of epoxy molding compound (EMC)

The effects of various curing accelerators on the physical properties of epoxy molding compounds (EMCs) were investigated. Such properties as elasticities in rubbery and glassy regions, glass transition temperature, thermal expansion coefficient, and water absorption at 60°C of neat epoxy resins using various curing accelerators were found to be directly reflected in the properties of the EMCs that were prepared by using each resin system. However, volume resistivity and saturated water absorption at 120°C were not reflected. This was attributed to differences in the catalytic reactivity of accelerators causing different melt viscosity for the EMC, which resulted in different densities (packing degrees) and affected physical properties of molded EMC. On the other hand, it was found that the density of molded EMC was also affected by the molding conditions. To improve the physical properties of the molded EMC, in addition to proper selection of accelerators, it was very important to set the melt viscosity of the EMC as high as possible within the moldable range and to select suitable molding conditions.     

Fabrication and characterization of Nb2O5-doped 3Y-TZP materials sintered by microwave technology

The purpose of this research is focused on the manufacture and characterization of a partially stabilized zirconia ceramic with 3 mol% of Yttria and doped with .5 and 1.5 mol% of Nb₂O₅ to analyze the influence of doping, with the purpose of improving the properties before hydrothermal degradation. In the first instance, the microwave sintering process was used for the consolidation of this material, then the physical and mechanical properties were characterized. Together, the results obtained by the conventional sintering process were compared. A low hydrothermal degradation study (LTD) is presented at low temperatures in which possible changes in the mechanical properties of the ceramic materials are analyzed and its influence on the phase transformation that zirconia may present is observed. The mechanical properties were evaluated through hardness, fracture toughness, and Young's modulus tests. Likewise, their density was analyzed, and microstructure was characterized by FESEM. It was found that the microwave-sintered samples at 1200°C exhibited superior properties of toughness than even samples sintered by conventional methods at higher temperatures (1400°C). The sample of 3Y-TZP with 1.5 mol% Nb₂O₅ sintered by microwave with <.2% of porosity achieved a maximum fracture toughness value around 40% higher than the dense monolithic 3Y-TZP material.     

Study of the solution properties of tactic polystyrenes

Summary Viscosity measurements are reported for syndiotactic polystyrenes in a molar mass range from 35,000 to 400,000 g/mol and standard fractions of narrowly distributed atactic polystyrenes in a molar mass range from 50,000 to 600,000 g/mol in trichlorobenzene at 135 °C. The correlation between molar mass and intrinsic viscosity of different polystyrene samples was investigated as well as their solution properties. The results demonstrate that the intrinsic viscosity of polystyrene in thermodynamically good solvents is independent of the type of tacticity of the polystyrenes investigated here. The dilute solution properties were compared with those for isotactic and atactic polystyrenes. The small differences in their solution viscosities may occur due to the different molar mass distributions of differently synthesized samples. Received: 14 April 1998/Revised version: 23 June 1998/Accepted: 23 June 1998     

Density, Surface Tension, and Viscosity of PbO-B2O3-SiO2 Glass Melts

The density, surface tension, and viscosity of the melts from the PbO-B₂O₃-SiO₂ system have been measured at temperatures in the range 1073–1473 K. The effect of composition on these properties was also investigated. The density of the melt was found to increase linearly with increasing PbO content. Molar volume was derived from the density data, and its deviation from the additivity of partial molar volumes was calculated. These deviations in molar volume from those obtained from additivity rules have been used along with the ratio of various coordination numbers of boron (as reported by Bray) to discuss the structure of the melts. The surface tension was found to decrease with decreasing SiO₂/B₂O₃ ratio, and to increase in the range of the PbO content between 30 and 60 mol%, showing a maximum at ∼60 mol% PbO, and then decreased with further additions. This result suggested that the surface tension would be affected primarily by the B₂O₃ content in the range of the PbO content between 30–60 mol%, and mainly by the PbO content in the range of the PbO content >60 mol%, respectively. The viscosity of the melt was found to decrease linearly with increasing PbO content. The results obtained indicate that the increase in viscosity with B₂O₃ was half that of SiO₂ (on a molar basis), and an empirical equation has been proposed for the viscosity as a function of mole fraction.     

A Novel Propolis Wax-Based Organogel: Effect of Oil Type on Its Formation,Crystal Structure and Thermal Properties

In this work, the potential application of propolis wax (PW) as a novel organogelator was investigated in different oils (canola, sesame, sunflower and flaxseed oil). PW at 2% (w/w) concentration produced a thick organogel at 5, 10 and 15 °C, with needle‐like crystals, suggesting that PW is a relatively efficient structuring agent for organogel formation. The oil binding capacity of the organogel with canola oil was lower than that of the other organogels, and the gelling time of flaxseed organogel with lower oil viscosity was shorter. The X‐ray diffraction measurements of the crystals showed β′‐form crystals, with no influence of oil type. In FTIR results, no chemical intermolecular interactions that were observed indicated physical bonds in the organogel network. DSC analysis was carried out to obtain greater insight into the thermal behavior of PW organogels. No significant differences were observed. The textural properties of PW organogels were stable over 30 days of storage. Flaxseed oil organogel had the greatest firmness and stickiness. These results showed the effect of oil viscosity on PW gel behavior.     

Effect of Li and Bi co-doping and sintering temperature on dielectric properties of PLZT 9/65/35 ceramics

In the present study, lead-lanthanum-zirconate-titanate (PLZT) ceramics were prepared by a solid-state mixed oxide method. Different amount of lithium carbonate and bismuth oxide (0.15 mol%, 0.45 mol% and 0.75 mol%), where the ratio of Li:Bi =1:1 by mole, was added to PLZT to investigate the effect of Li and Bi co-doping. The ceramic samples were sintered at the temperatures of 1000, 1050, 1100, 1150 and 1200 °C for 4 h. After that, all samples were subjected to phase identification, physical property determination (sintered density and microstructure) and dielectric property measurement. It was found that doping of 0.15 mol% Li and Bi resulted in maximum dielectric constant (ε_r =7819) when sintered at 1200 °C. Grain size of PLZT ceramics was dependent on sintering temperature and dielectric properties were affected by the chemical composition rather than the grain size of the ceramics. Therefore, co-doping of Li and Bi was useful as it could improve the dielectric properties of PLZT ceramics.     

Silane grafting and moisture crosslinking of polypropylene

Peroxide initiated vinylsilane grafting of polypropylene in an intensive mixer, and the subsequent water crosslinking process were studied. Different concentrations of vinyl trimethoxysilane and dicumyl peroxide were used. The materials obtained after mixing in the rheocord were hot pressed at 190°C. The melt viscosity of the obtained sheets, the melting enthalpy and melting temperature (DSC, differential scanning calorimetry), the mechanical properties and the thermal decomposition behavior (TG, thermogravimetric analysis) were studied. No evidence of grafting during the rheocord processing was observed. Nevertheless, for the hot pressed sheets with concentrations higher than 4 phr of vinyl silane an important increase in the melt viscosity was observed. This increase agrees with the change observed in the mechanical properties, which show a maximum for the water crosslinked samples containing 4 phr of vinyl silane. The modulus increases by 39% at 90°C and 33% at 130°C, while the tensile strength rises by ～22% at both temperatures. The silane grafted water crosslinked samples show a more stable thermal behavior than both the silane grafted samples and the unmodified polypropylene.     

Synthesis and Optimization of 2-ethylhexyl Ester as Base Oil for Drilling Fluid Formulation

A stable ester was synthesized to overcome the ester hydrolysis problem during the drilling of oil or gas wells using a conventional ester-based drilling fluid. The thermal and hydrolytic stability of the produced ester was high owing to the transesterification method employed in this study. The reaction was performed using 2-ethylhexanol and methyl laureate esters in the presence of sodium methoxide as a catalyst. In order to obtain the optimum synthesis conditions, a response surface methodology (RSM) was appraised based on the central composite design (CCD). The optimum conditions were determined as follows: 0.6 wt.% catalyst, 70°C reaction temperature, 1:1.5 molar ratio, and 11.5 min of reaction time. The results of 77 wt.% 2-ethylhexyl ester (2-EH) illustrated a high agreement between the experimental and RSM models. The reaction product contained 77 wt.% 2-EH and 23% 2-ethylhexanol. The kinematic viscosity was 5 mm²/s at 40°C and 1.5 mm²/sec at 100°C; the specific gravity was 0.854, flash point was 170°C, and pour point was ?7°C. The produced product showed similar properties to the available commercial product. However, it was observed that the mud formulation using the synthesized base oil had superior rheological properties at 121°C.     

Biodiesel from canola oil using a 1 : 1 molar mixture of methanol and ethanol

Canola oil was transesterified using a 1 : 1 molar mixture of methanol and ethanol (M/E) with potassium hydroxide (KOH) catalyst. The effects of catalyst concentration (0.5–1.5 wt‐%), molar ratio of M/E to canola oil (3 : 1 to 20 : 1) and reaction temperature (25–75 °C) on the percentage yield measured after 2.5 and 5.0 min were optimized using a central composite design. A maximum percentage yield of 98% was obtained for a catalyst concentration of 1.1 wt‐% and an M/E to canola oil molar ratio of 20 : 1 at 25 °C at 2.5 min, whereas a maximum percentage yield of 99% was obtained for a catalyst concentration of 1.15 wt‐% and all molar ratios of reactants at 25 °C at 5 min. Statistical analysis demonstrated that increasing catalyst concentration and molar ratio of reactants resulted in curvilinear and linear trends in percentage yield, both at 2.5 and 5 min. However, reaction temperature, which affected the percentage yield at 2.5 min linearly, was insignificant at 5 min. The resultant mixed methyl/ethyl canola esters exhibited enhanced low‐temperature performance and lubricity properties in comparison to neat canola oil methyl esters and also satisfied ASTM D6751 and EN 14214 standards with respect to oxidation stability, kinematic viscosity, and acid value.     

Rheological properties and sensory texture of mayonnaise

Mayonnaises are viscoplastic oil‐in‐water emulsions, in which rheological properties have important influences on functional properties and the sensory quality. A set of 17 samples of both traditional and light mayonnaises were tested at 10 and 25 °C, using a rheoviscometer Rotovisco RT 10. Nonlinear relations were observed between the yield value and the apparent viscosity. The yield value was correlated with several sensory characteristics rated after manipulation with a spoon, but not in oral testing. No relations were obtained between the apparent viscosity and sensory characteristics. The yield value and the texture acceptability were related significantly to the flavour acceptability. Multivariate statistical techniques were found advantageous for improving the prediction of the texture acceptance.     

Preparation and characterization of carbon fibers from polyacrylonitrile precursors

The present work deals with the preparation of carbon fibers from polyacrylonitrile (PAN) fibers. The chemical composition and physical properties of the starting fibers were determined. The PAN fibers were stabilized in air at the temperatures (230, 270, and 300°C) with the heating time from 40 to 420 min. The effects of both final stabilization temperature and heating rate on the chemical and physical properties of the prepared stabilized fibers were studied. The chosen stabilized fibers samples were carbonized in argon atmosphere at the temperatures (1000, 1200, and 1400°C) with different heating rates 5, 10, 15, and 20°C min^?1. The effects of both carbonizing temperature and heating rate on the weight loss, density, elemental composition, and IR absorption spectra of carbonized fibers were also studied. The fiber sample, which was carbonized at 1400°C, contains 97.55% carbon, 1.75% nitrogen, and 1.4% hydrogen. This means that carbonizing the stabilized fibers at 1400°C in argon atmosphere is suitable to get oxygen‐free carbon fibers. Therefore, the used carbonizing temperature in the present work (1400°C) is suitable to produce moderate heat‐treated carbon fibers with the heating rate of 15°C min^?1. The modulus of the prepared carbon fibers was compared to that of industrially produced fibers using the results of X‐ray analysis. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Colored amorphous silica-based powder with TiN nanocrystals precipitated by ammonolysis of Ti–Si–O ternary glass

Coloration of amorphous silica powder containing titania was investigated by nitridation in an ammonia flow. The oxide precursors were obtained by the hydrolysis of a mixture of tetraethyl orthosilicate (TEOS) and tetrabutoxy titanium (TBT). The color changed with the amount of TBT in the mixture, the hydrolysis pH and the ammonolysis temperature. The original white color of the 8 mol% TBT powder hydrolyzed under basic pH conditions changed to pale goldenrod at 700°C, then to dark olive green at 800°C, and further darkened with increasing ammonolysis temperature. A steel-blue color appeared at 900°C for the powder obtained with 3 mol% TBT, and increased in darkness at 1000°C. A similar bluish color was observed for powders obtained by acidic hydrolysis after ammonolysis above 900°C, and this was independent of the amount of titania, although the chroma decreased with increasing firing temperature for the powder with 3 mol% TBT. The ammonolysis powder products were characterized using X-ray diffraction (XRD), electron probe micro analysis (EPMA), transmission electron microscopy-electron energy-loss spectroscopy (TEM-EELS), scanning transmission electron microscopy-high-angle annular dark-field imaging (STEM-HAADF) and Ti–K edge X-ray absorption fine structure (XAFS). The color change was related to both precipitated TiN nanocrystals and residual titanium in the amorphous silica matrix. The TiN exhibited a goldish reflection and also plasmonic absorption from light blue to gray depending on the TiN crystallite size. The plasmonic absorption and resonance of nanocrystalline TiN will be useful similarly to that of gold in nanotechnology for various kinds of energy application.     

Structure and properties of a poly(amino ether) resin after reprocessing in the melt state

The effects of reprocessing by extrusion for up to five cycles, at both the usual (200°C) and an extreme (230°C) temperature, on the structure and mechanical properties of a poly(amino ether) (PAE) resin were studied. A slight darkening and viscosity increase was observed, mainly upon reprocessing at 230°C. The melt flow index and solubility analysis indicated that grafting and crosslinking reactions took place, respectively, after reprocessing at 200 and 230°C. The Young′s modulus and the yield stress of PAE increased slightly with successive extrusion cycles. This was attributed to the viscosity‐induced increase in orientation, and to a minor extent to the partially grafted/crosslinked nature of the samples. The decrease in the ductility was more noticeable in the samples reprocessed at 230°C, and was attributed to the reduced ability to elongate of partially grafted and partially crosslinked structures present after reprocessing, respectively, at 200 and 230°C. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1368–1373, 2006     

Comparison between microwave and conventional sintering on the properties and microstructural evolution of tetragonal zirconia

In this research, the comparison between microwave sintering and conventional sintering on the mechanical properties and microstructural evolution of 3?mol% yttria-stabilised zirconia were studied. Green bodies were compacted and sintered at various temperatures ranging from 1200?°C to 1500?°C. The results showed that microwave assisted sintering was beneficial in enhancing the densification and mechanical properties of zirconia, particularly when sintered at 1200?°C. It was revealed that as the sintering temperature was increased to 1400?°C and beyond, the grain size and mechanical properties for both microwave- and conventional-sintered ceramics were comparable thus suggesting that the sintering temperature where densification mechanism was activated, grain size was strongly influenced by the sintering temperature and not the sintering mode.     

Enzymatic modification of triacylglycerols of high eicosapentaenoic and docosahexaenoic acids content to produce structured lipids

Immobilized lipase, IM60, from Rhizomucor miehei was used as a biocatalyst for the incorporation of capric acid (C10:0) into fish oil originally containing 40.9 mol% eicosapentaenoic (20:5n-3) and 33.0 mol% docosahexaenoic (22:6n-3) acid. Acidolysis was performed with and without organic solvent. Pancreatic lipase-catalyzed sn-2 positional analysis was performed after enzymatic modification. Tocopherol analysis was performed before and after enzymatic modification. Products were analyzed by gas-liquid chromatography. After a 24-h incubation in hexane, there was an average of 43.0±1.6 mol% incorporation of C10:0 into fish oil, while 20:5 and 22:6 decreased to 27.8±2.2 and 23.5±1.3 mol%, respectively. The solvent-free reaction produced an average of 31.8±8.5 mol% C10:0 incorporation, while 20:5 and 22:6 decreased to 33.2±3.3 and 28.3±3.9 mol%, respectively. The effect of incubation time, substrate molar ratio, enzyme load, and added water were also studied. In general, as the enzyme load, molar ratio, and incubation time increased, mol% C10:0 incorporation also increased. The optimal mol% C10:0 incorporation was 41.2% at 48 h for the reaction in hexane and 46.4% at 72 h for the solvent-free reaction. The highest C10:0 incorporation (65.4 mol%) occurred at a molar ratio of 1:8 (fish oil triacylglycerols/capric acid) in hexane. For the solvent-free reaction, the optimal mol% C10:0 incorporation (56.1 mol%) occurred at a molar ratio of 1:6. An enzyme load of 10% gave the highest mol% C10:0 incorporation (41.4 mol%) in hexane; the highest incorporation (38.3 mol%) for the solvent-free reaction occurred at 15% enzyme load. Mol% incorporation of C10:0 declined with increasing amounts of added water. The optimal mol% C10:0 incorporation occurred at 1% added water (47.9 mol%) for the reaction in hexane, and at zero added water for the solvent-free reaction (21.8 mol%). Fish oil containing capric acid was successfully produced and may be nutritionally more beneficial than unmodified oil.