The Surface and Thermodynamic Properties of Ethoxylated Sodium Monoalkyl Sulfosuccinate Surfactants

A series of ethoxylated sodium monooctyl sulfosuccinates [E(n)SMOSS] and ethoxylated sodium monolauryl sulfosuccinates [E(n)SMLSS] have different units of ethylene oxide (n = 9, 14, 23) were synthesized. The surface and thermodynamic properties of these surfactants have been compared with sodium dioctyl sulfosuccinate surfactant (SDOSS) as a commonly used surfactant. The surface tension measurements at 25, 35, 45, and 55°C were used to determine of the critical micelle concentration (CMC) and surface active properties of these surfactants. The effect of the ethylene oxide (EO) unit and the alkyl chain length on the surface properties for the prepared surfactants was studied. The results show that the ethoxylated sodium monoalkyl sulfosuccinates generally have lower values of CMC than that of sodium dioctyl sulfosuccinate. The values of surface active parameters indicate that the ethoxylated sodium monooctyl sulfosuccinates and ethoxylated sodium monolauryl sulfosuccinates surfactants have adsorption properties better than the sodium dioctyl sulfosuccinate surfactant as a resulted presence of ethylene oxide in molecules of the prepared surfactants. The thermodynamic parameters show that the (EO) unites in the chemical structure of ethoxylated sodium monoalkyl sulfosuccinate surfactants improve their micellization and adsorption properties.     

Use of blowing catalysts for integral skin polyurethane applications in a controlled molecular architectural environment: Synthesis and impact on ultimate physical properties

Polyurethane elastomers of a controlled molecular architecture were synthesized using a two‐step polymerization technique. The building blocks of the elastomeric materials included urea–urethane prepolymers end‐capped with diisocyanate groups and had an exact number of urea groups at both ends. Two‐dimensional bifurcated hydrogen‐bonding networks incorporating the urea groups were, with differential scanning calorimetric and dynamic mechanical thermal analyzer techniques, responsible for the increase in the glass‐transition temperature (T_g) of the hard block and sharp interface morphology between the pure “hard” domains and pure “soft” domains. The higher extent of the phase separation between the two phases contributed to higher elastic moduli for the hard blocks and higher tensile strength for the elastomeric samples. Higher elongation values were attributed to the liberation of the elastomeric chain ends that otherwise would have been constrained in the interface region. The higher T_g values of the hard blocks corresponded to an increase in the hardness values and a decrease in the tear‐strength values. The increase in the amount of urea groups within the hard segments, as a result of the increased amount of water and blowing catalyst, resulted in elastomeric foams with higher open‐cell content. This resulted in lower resilience values as measured using the pendulum rebound test and was attributed to the ability of the open cells to absorb and dissipate energy. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2526–2536, 2002     

Synthesis and in vitro anticancer activity of some novel tetrahydroquinoline derivatives bearing pyrazol and hydrazide moiety

A new series of tetrahydroquinoline derivatives having pyrazol and hydrazide moieties were synthesized for the purpose of anticancer cell line evaluation. Syntheses of these compounds were firstly achieved by one pot four reactions. The reaction of 3-amino-tetrahydro-1H-pyrazolo [3,4-b]quinolin with aldehydes, indoline-2,3-dione derivatives to give 9a-c , 11a-c , and 13a,b , respectively. In similar manner for biological comparison, the reactions of compound 5 with the same aldehydes and indoline-2,3-dione derivatives to give 19a-c and 20a-c . The newly synthesized compounds were examined in vitro for their cytotoxic activity against HepG-2 and A549 cancer cells. The compounds 11a-c and 20a-c showed promising activity as anticancer agents against HepG-2 and A549 cancer cells.     

Synthesis and Characterization of Self-Assembling Some Thiol Surfactants on Gold Nanoparticles

The purpose of this work is to study the self-assembling of some synthesized thiol surfactants namely (mercaptopropane-, mercaptohexane-, mercaptooctane-, and mercaptodecane sodium sulfonate) on the fabricated gold nanoparticles. The self-assembling of these surfactants on gold nanoparticles characterized using different techniques such as FTIR spectroscopy, UV spectroscopy, and transmission electron microscopy (TEM). Spectroscopic evidence suggests that the synthesized thiol surfactants have been attached to the gold nanoparticles. The effect of self-assembling of these surfactants on the size of the gold nanoparticles was studied using TEM images. The growth of the gold nanoparticles was investigated with respect to the increase of alkyl chain in the synthesized thiol surfactants. The results show that the stabilization of gold nanoparticles was affected by the increase in alkyl chain length of these surfactants. The effect of gold nanoparticles on the interfacial tension and the emulsion stability of these surfactants with crude oil was studied.     

Thermal radiation effects on MHD flow past a semi-infinite inclined plate in the presence of mass diffusion

MHD mixed free-forced heat and mass convective steady incompressible laminar boundary layer flow of a gray optically thick electrically conducting viscous fluid past a semi-infinite inclined plate for high temperature and concentration differences is studied. A uniform magnetic field is applied perpendicular to the plate. The density of the fluid is assumed to reduce exponentially with temperature and concentration. The usual Boussinesq approximation is neglected due to the high temperature and concentration differences between the plate and the ambient fluid. The Rosseland approximation is used to describe the radiative heat flux in the energy equation. The boundary layer equations governing the flow are reduced to ordinary differential equations, which are numerically solved by applying an efficient technique. The effects of the density/temperature parameter n, the density/concentration parameter m, the local magnetic parameter M_x and the radiation parameter R are examined on the velocity, temperature and concentration distributions as well as the coefficients of skin-friction, heat flux and mass flux.     

Water-dispersible sugar-coated iron oxide nanoparticles. An evaluation of their relaxometric and magnetic hyperthermia properties

Synthesis of functionalized magnetic nanoparticles (NPs) for biomedical applications represents a current challenge. In this paper we present the synthesis and characterization of water-dispersible sugar-coated iron oxide NPs specifically designed as magnetic fluid hyperthermia heat mediators and negative contrast agents for magnetic resonance imaging. In particular, the influence of the inorganic core size was investigated. To this end, iron oxide NPs with average size in the range of 4-35 nm were prepared by thermal decomposition of molecular precursors and then coated with organic ligands bearing a phosphonate group on one side and rhamnose, mannose, or ribose moieties on the other side. In this way a strong anchorage of the organic ligand on the inorganic surface was simply realized by ligand exchange, due to covalent bonding between the Fe(3+) atom and the phosphonate group. These synthesized nanoobjects can be fully dispersed in water forming colloids that are stable over very long periods. Mannose, ribose, and rhamnose were chosen to test the versatility of the method and also because these carbohydrates, in particular rhamnose, which is a substrate of skin lectin, confer targeting properties to the nanosystems. The magnetic, hyperthermal, and relaxometric properties of all the synthesized samples were investigated. Iron oxide NPs of ca. 16-18 nm were found to represent an efficient bifunctional targeting system for theranostic applications, as they have very good transverse relaxivity (three times larger than the best currently available commercial products) and large heat release upon application of radio frequency (RF) electromagnetic radiation with amplitude and frequency close to the human tolerance limit. The results have been rationalized on the basis of the magnetic properties of the investigated samples.     

NIRSE: Normal-incidence rotating-sample ellipsometer

We describe a normal-incidence rotating-sample ellipsometer (NIRSE) which is capable of measuring the ratio of the complex amplitude reflection coefficients of an anisotropic sample for incident light that is linearly polarized along two orthogonal principal axes in its surface. In the NIRSE, is derived from the normalized amplitudes of the Fourier components of a photoelectric signal at double and four times the angular frequency of sample rotation. The application of PIE (perpendicular-incidence ellipsometry) to anisotropic film-substrate systems is also discussed.     

Separability of amplitude,phase and polarization information in the Jones calculus

The two-component Jones vector is cast in a form that achieves the separation of the information on the polarization ellipse from that on the amplitude and phase of the light wave. The shape, sense of rotation and orientation of the elliptic vibration of the electric field are described by the complex polarization variable χ while the amplitude a (size) and temporal phase ? of that vibration are described by the complex amplitude A = aexp(i?). The transformation of the complex amplitude of the wave A after passing through an optical system leads to a complex-amplitude transfer function (CATF) which is a nonanalytic function of the complex polarization variable χ. The CATF is, in turn, separable into polarization-dependent (real) amplitude and phase transfer functions (ATF and PHTF). Together with the polarization transfer function PTF (the transformation of χ), the ATF and PHTF provide a useful set of tools that complement the well-known Jones calculus.     

Equalization of reflectance of parallel-polarized electromagnetic plane waves at normal and oblique incidence of interfaces between transparent media and its use for measurement of the dielectric constant

A new angle of incidence of significance, when considering the reflection of electromagnetic waves at interfaces between transparent media, is defined. At this angle, denoted by φ_e, the reflection coefficient of parallel-polarized radiation is equal in magnitude and opposite in sign to the reflection coefficient at normal incidence. No similar angle exists for the perpendicular polarization. If ε is the relative dielectric constant, i.e., the ratio of the dielectric constant of the medium of refraction to that of the medium of incidence, we find that tan φ_e=(ε²+ε)^1/2. Measurement of φ_e, by equalization of the absolute (intensity) reflectances at normal and oblique incidence, allows ε to be determined using the inverse relation ε=(tan²φ_e+1/4)^1/2−1/2.