Presence Of Ester Functional Groups Research Articles

Effect of the Alkyl Density of Acrylic Acid Ester on the Viscosity-Reducing Effect of Polycarboxylate Superplasticizer.

Concrete is vital for the development of modern buildings. However, they suffer from the high viscosity problem in their application process due to the use of a low water-cement ratio in order to maintain their high strength. Developing PCEs with the presence of ester functional groups in their molecular structure is one of the most effective measures to improve the flowability of concrete. Here, three PCEs with different alkyl densities of acrylic acid ester: PCE-M, PCE-E, and PCE-B were designed to explore their viscosity-reducing effect on the performance of cement and concrete. The structures of the three PCEs were characterized via Fourier transform infrared (FTIR) spectra, proton nuclear magnetic resonance (1H NMR), and gel permeation chromatography (GPC). Their properties were also determined via zeta potential, surface tension, and rheological experiments. It was found that PCE-M had the best performance, with the lowest surface tension, highest zeta potential, and therefore highest charge density on the cement particles, lowest viscosity, and highest flowability of cement paste, and exhibited the best performance of concrete in terms of workability. The best performance of PCE-M in reducing the viscosity of cement and concrete can be ascribed to the smallest amount of water-repellent alkyl groups, enhancing the electrostatic repulsion and reducing the viscosity, thereby boosting the dispersion and stabilization of cement pastes and concrete. This study shed lights on designing other PCEs with high viscosity-reducing effects via an ester group control.

Effect of Citric Acid on the Properties of Sapwood of Pinus sylvestris Submitted to Thermomechanical Treatment

The present study aimed to evaluate the effect of citric acid on the properties of solid pine wood, which were submitted to thermomechanical treatment. A preliminary test was performed in a previous study to evaluate the influence of different temperatures of pressing and concentrations of citric acid on the physical properties of wood. After choosing the best treatments (170 °C and 5% and 10% of citric acid), the effect of these on the chemical properties (SEM, FTIR and pH); on the density profile using an X-ray microtomography and on the resistance to aging through an abrasion test were evaluated. The result of the chemical analysis showed an increase of the presence of ester functional groups, as well as better coverage and higher acidity of the surface. The density profile technique allowed us to observe the formation of peaks of density on the surface where the acid was applied. Lastly, it was also possible to verify an increase in the resistance to abrasions because of the application of citric acid.

Monodisperse copolymer nanosphere assembly by miniemulsion polymerization

Hydrophobic monomer 1-octene/ethylene with less hydrophobic monomer methyl methacrylate is used to produce copolymer of high molecular weights nanoparticles with narrow molecular weight distribution by mini emulsion polymerization. Concomitant results from dynamic light scattering (DLS) analysis and scanning electron microscope (SEM) analysis divulges the development of nano-scaled polymeric spheres with nearly uniform particle size distribution. Spectroscopy techniques (FT-IR and 1H NMR) confirms the presence of ester functional group as well as methylene group in the copolymer. With increase in olefinic concentration in the monomer feed increases its specific signals for only methylene proton in the copolymer. Thermal properties of the copolymers established by thermogravimetric analysis (TG) methods exhibits good thermal stability up to a temperature of 400°C.

Cleavage of PO in the Presence of P–N: Aminophosphine Oxide Reduction with In Situ Boronation of the PIII Product

In contrast to tertiary phosphine oxides, the deoxygenation of aminophosphine oxides is effectively impossible due to the need to break the immensely strong and inert PO bond in the presence of a relatively weak and more reactive PN bond. This long-standing problem in organophosphorus synthesis is solved by use of oxalyl chloride, which chemoselectively cleaves the PO bond forming a chlorophosphonium salt, leaving the PN bond(s) intact. Subsequent reduction of the chlorophosphonium salt with sodium borohydride forms the P(III) aminophosphine borane adduct. This simple one-pot procedure was applied with good yields for a wide range of PN-containing phosphoryl compounds. The borane product can be easily deprotected to produce the free P(III) aminophosphine. Along with no observed PN bond cleavage, the use of sodium borohydride also permits the presence of ester functional groups in the substrate. The availability of this methodology opens up previously unavailable synthetic options in organophosphorus chemistry, two of which are exemplified.

Influence of Ester Functional Groups on the Liquid-Phase Structure and Solvation Properties of Imidazolium-Based Ionic Liquids

The incorporation of ester functions in the side chains in 1-alkyl-3-methylimidazolium cations seems to increase the biodegradability of these ionic liquids. We study here how the presence of ester functional groups affects the liquid-state structure (namely, the microphase segregation between polar and nonpolar domains in these ionic liquids) and the way in which the solvation of gases can be understood in these solvents. We use molecular simulation to study the structure of the ionic liquids 3-methyl-1-(pentoxycarbonylmethyl)imidazolium octylsulfate, [C(1)COOC(5)C(1)im][C(8)SO(4)]; and 3-methyl-1-(pentoxycarbonylmethyl)imidazolium bis(trifluoromethylsulfonyl)imide, [C(1)COOC(5)C(1)im][NTf(2)] in the liquid phase and to assess the molecular mechanisms of solvation of carbon dioxide and ethane. The presence of ester functions influences the relative size of the polar and nonpolar domains in the ionic liquids, but does not significantly affect the solvation of gases.

Spectrophotometric Determination of Certain Cephalosporins Using Ferrihydroxamate Method

Cephalexin, cefixime, ceftriaxone and cefotaxime were determined spectrophotometrically in the pure form and in pharmaceutical formulations by using ferrihydroxamate method. Reaction optimization with respect to reaction time and temperature has been investigated. Influence of the presence of ester functional group on the determination of cephalosporins as ß-lactams under conditions optimized was evaluated. Using cefotaxime sodiume as model drug with ester functional group, it was shown that proposed method gives equally acurate and precise results even in the presence of ester functional group.