The effectuation of seawater on the microstructural features and the compressive strength of fly ash blended cement at early and later ages

The current work scrutinizes the effectuation of seawater on morphological properties, pore structure, and compressive strength during the hydration process of fly ash blended cement at 3, 7, 28, 56, and 90 days to better understand the influence of salinity conditions of seawater on the microstructural modification and strength development of the hydration products as well as the total porosity. The chemical reaction's mechanism of mightily soluble salts, for example, Mg₂SO₄ and NaCl, with hydrated fly ash and blended cement (calcium-bearing phases) was also confirmed. Fourier-transform infrared spectroscopy has been appointed to observe and characterize the energetics of variation in the formulation of portlandite (CH), calcium silicate hydrate, gypsum (Gy), ettringite (AFt), and calcium chloroaluminate (Friedel's salt [FS]) throughout the hydration process of fly ash blended cement with seawater in comparison with deionized water. X-ray diffraction analysis exposed that the peak intensities of FS, portlandite, and some particular phases of the hydrated fly ash blended cement in seawater are higher and sharper than the comparable peaks in deionized water. Mercury intrusion porosimetry-measurements have been appointed that the total porosity of artificial seawater (ASW) was decreased from 28.9% at 3 days to 19.4% at 56 days. In addition, the average, median, and critical pore diameter were decreased in ASW while compared to deionized water (DIW). The reaction products of this work were also characterized using scanning electron microscopy, EDS, compressive strength, and isothermal calorimeter.     

The depth profiling of TiO2 pigmented coil coatings using step scan phase modulation photoacoustic FTIR

The depth distribution of a TiO₂ pigment within the polyurethane (PU) coil coatings is investigated using step scan phase modulation photoacoustic (SS-PM-PA) FTIR. Coil coatings with different pigment contents were prepared and the modulation frequency (MF) of the SS-PM-PA FTIR varied to record the depth distribution of the pigment within the coating. The TiO₂ pigment was shown to contribute significantly to the SS-PM-PA FTIR signal. A TiO₂ aggregated region within the topcoat is found close to the topcoat-primer interface and further away from the topcoat surface. A deeper TiO₂ aggregated region can be identified when pigment content is relatively low. The SS-PM-PA FTIR signal shows a considerable contribution from the primer originated signal, provided the TiO₂ pigment content is sufficiently high and the modulation frequency applied is relatively low. SEM cross-section imaging results show a strong correlation of the TiO₂ depth distribution with SS-PM-PA FTIR results, which confirms the applicability of the SS-PM-PA FTIR technique to the depth profiling study of TiO₂ pigmented coil coatings.     

AFM/FTIR: A New Technique for Materials Characterization

A new type of infrared spectroscopy for obtaining the molecular composition of the surfaces of materials at ultra-high spatial resolution has been developed by combining atomic force microscopy (AFM) with Fourier-transform infrared spectroscopy (FTIR). This new analytical technique involves the use of an AFM to detect the response of a material to the absorption of modulated infrared radiation from an FTIR spectrometer and is referred to as AFM/FTIR spectroscopy. When the technique of AFM/FTIR spectroscopy is completely developed, we plan to use it to probe the molecular structure of interphases in polymer composites and adhesive bonds. Two approaches have been used to measure the response of polymer systems to infrared absorption. The first involves the use of a contact mode AFM probe to measure the thermal expansion of the polymer; the second involves using a scanning thermal microscopy (SThM) probe to measure the polymer's temperature increase. In either case, the output of the probe resembles an interferogram to which a Fourier-transform can be applied to obtain the infrared absorption spectrum. The first approach was used to obtain excellent quality AFM/FTIR spectra from various neat polymer films, including polystyrene, polycarbonate, and a model adhesive system consisting of an epoxy resin cross-linked with dicyandiamide. Excellent spectra were also obtained from polystyrene beads having a diameter of about 2 µm. The second approach, using an SThM probe to determine the temperature increase that accompanies infrared absorption, was also used to obtain interferograms of polymer samples such as polystyrene. However, the interferograms were noisy and the AFM/FTIR spectra obtained from them had a low signal-to-noise ratio. The present results, thus, show that AFM/FTIR spectroscopy is feasible but the spatial resolution of the technique remains to be shown.     

Ionic conductivity,dielectric behavior,and HATR–FTIR analysis onto poly(methyl methacrylate)–poly(vinyl chloride) binary solid polymer blend electrolytes

Solid polymer electrolytes comprising blends of poly(vinyl chloride) (PVC) and poly(methyl methacrylate) (PMMA) as host polymers and lithium bis(trifluoromethanesulfonyl) imide (LiTFSI) as dopant salt were prepared by solution‐casting technique. The ionic conductivity and dielectric behavior were investigated by using AC‐impedance spectroscopy in the temperature range of 298–353 K. The highest ionic conductivity of (1.11 ± 0.09)×10^?6 S cm^?1 is obtained at room temperature. The temperature dependence of ionic conductivity plots showed that these polymer blend electrolytes obey Arrhenius behavior. Conductivity–frequency dependence, dielectric relaxation, and dielectric moduli formalism were also further discussed. Apart from that, the structural characteristic of the polymer blend electrolytes was characterized by means of horizontal attenuated total reflectance–Fourier transform infrared (HATR–FTIR) spectroscopy. HATR–FTIR spectra divulged the interaction between PMMA, PVC, and LiTFSI. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Properties and antimicrobial activities of starch–sodium alginate composite films incorporated with sodium dehydroacetate or rosemary extract

Antimicrobial films were prepared with oxidized and acetylated corn starch–sodium alginate by incorporating sodium dehydroacetate or rosemary extract. Films incorporated with sodium dehydroacetate ≥ 0.1% or rosemary extract ≥ 0.3% had an anti‐Escherichia coli effect. Aspergillus niger could be effectively inhibited by the incorporation of sodium dehydroacetate ≥ 0.3%. Rosemary extract showed no inhibitory effect on Aspergillus niger. Sodium dehydroacetate and rosemary extract reduced the tensile strength and elongation at break, and increased the water vapor permeability of the films. Sodium dehydroacetate made the films more greenish–yellow with the increase of sodium dehydroacetate concentration. The color of the films became darker and more reddish–yellow as rosemary extract was increased. Fourier transform infrared (FTIR) spectra analysis revealed that sodium dehydroacetate and rosemary extract reduced starch crystallinity. The surface of the films became rougher as a result of an addition of sodium dehydroacetate and rosemary extract. These findings had potential applications in prolonging food shelf life based on different needs. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Synthesis and characterization of proton conducting polymer electrolyte based on poly(N‐vinyl pyrrolidone)

This work aims at developing and characterizing a proton conducting polymer electrolyte based on Poly(N‐vinyl pyrrolidone) (PVP) doped with ammonium bromide (NH₄Br). Proton conducting polymer electrolytes based on PVP doped NH₄Br in different molar ratios have been prepared by solution casting technique using distilled water as solvent. The XRD pattern confirms the dissociation of salt. The FTIR analysis confirms the complex formation between the polymer and the salt. The conductivity analysis shows that the polymer electrolyte with 25 mol % NH₄Br has the highest conductivity equal to 1.06 × 10^?3 S cm^?1 at room temperature. Also it has been observed that the activation energy evaluated from the Arrhenius plot is low (0.50 eV) for 25 mol % NH₄Br doped polymer electrolyte. The influence of salt concentration on dc conductivity and activation energy of the polymer electrolyte has been discussed. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Distribution of Anionic Groups in TMP Suspensions

Abstract

The distribution of anionic groups in fibres, fines, the colloidal fraction, and the dissolved fraction of thermomechanical pulp (TMP) suspensions was determined. The influence of extraction, alkaline treatment, and peroxide bleaching of spruce TMP were also studied.

Spruce TMP was extracted with hexane, treated with alkali, or bleached with peroxide. Suspensions were made at pH 5.5 or 8, and fractionated into long fibres, large fines, small fines, a colloidal fraction, and a dissolved fraction. The surface and total charge of the fractions were determined separately by polyelectrolyte titration. To determine the origin of the charges, the contents of fatty acids, resin acids, and acidic units in polysaccharides in the different fractions were determined by gas chromatography.

Extraction of TMP with hexane prior to fractionation increased the measured total and surface charge of the fibres. The removal of wood resin probably uncovered some anionic groups on the fibre surface, or improved the penetration of the polymers into the pores of the fibres. The total charge, determined with polybrene titration, of the fines and the colloidal fraction was lower when the resin had been removed, while the surface charge, determined with poly-DADMAC, was not greatly affected.

Alkaline treatment of the TMP increased both the total charge and the surface charge of the fibres and fines, mainly because of demethylation of pectins. Alkaline treatment also increased the total and surface charge of the dissolved substances, due to the release of pectic acids into the water phase. Alkaline peroxide bleaching further increased the total and surface charge of fibres and dissolved substances, most likely due to oxidation of lignin. The total charge and the surface charge of the colloidal substances, consisting mainly of wood resin, were only slightly affected by alkaline treatment and peroxide bleaching.

The anionic charge in TMP suspensions originated mainly from free uronic acids in the xylans, arabinogalactans, and pectic acids. The contribution from the fatty and resin acids was substantial only for the colloidal fraction.     

Studies on the Effect of Polyamide-6 onto Modified Polyphenylene Oxide Matrix in Presence of Fumaric Acid as a Compatibilizer

Polymer blends of modified polyphenylene oxide (mPPO) and polyamide-6 (PA-6) are immiscible and incompatible in nature. However fumaric acid (FA) is used as a compatibilizer for the compatibilizing of mPPO/PA-6 blend systems. During melt compounding functional groups of the polymer components were reacted in the presence of a compatibilizer in the extruder. The blends were characterized by using FTIR, SEM, and mechanical behavior testing. The concentration of FA compatibilizer varies inversely w.r.t. PA-6 concentration in the blend systems. However the blend composition of PA-6 (10%) shows good miscibility among the other blend systems under present study.     

Aging of HDPE Pipes Exposed to Diesel Lubricant

The effects caused upon the physicochemical behavior of high-density polyethylene pipes by exposure to a diesel lubricant were investigated, as a function of time and temperature, by thermogravimetric and gravimetric analysis and by FT-IR. The gravimetric data were satisfactorily described using Fick's law. The fitting of the experimental points showed that diesel, which can be regarded as a model fluid to analyze the effects caused by aromatic unities present in oil derivatives, has a high diffusion rate into HDPE. The FT-IR results showed that no main structural modifications have occurred after exposure, besides solubilization of low molecular weight units. From the analysis performed, physical aging was identified as the aging process occurring when the HDPE pipes came in contact with diesel lubricant.     

Surface characterization of sulfated zirconia and its catalytic activity for epoxidation reaction of castor oil

The solid acid catalysts SO₄^2?/ZrO₂ were prepared by impregnation technique at different calcination temperatures. The surface characterizations were carried out by using scanning electron microscope (SEM), Fourier transform infrared spectrometer (FTIR), X-ray diffraction (XRD), temperature programed desorption of NH₃ (NH₃-TPD), and N₂-BET. The SEM results showed that the size of the SO₄^2?/ZrO₂ was not uniform and varied from about 1 to 20?µm. The characteristic peaks in FTIR spectra were essentially the same within the calcination temperature range of 400–700?°C. The XRD results indicated that the transition temperature from amorphous to tetragonal phase was up to 500?°C. The strong acid and superacid sites of the samples could be observed by the NH₃-TPD results. The largest BET surface area was 140 m²/g, when the calcination temperature was at 500?°C, and all the pore size distributions belong to mesoporous range. The solid acid SO₄^2?/ZrO₂ was used for the epoxidation of castor oil. When the calcination temperature of SO₄^2?/ZrO₂ was 600?°C, reaction temperature 45?°C, and reaction time 8?h, the reaction effect was better with an iodine value of 33.0?±?1.6?g/100?g and an epoxy value of 2.45?±?0.11?mol/100?g.