Microemulsion breakdown by pervaporation technique: Effect of the alkyl chain length of n-alkanol, a cosurfactant of the microemulsion

Two sets of microemulsions, cyclohexane- and water-rich ones, were prepared with the following n-alkanols as cosurfactants: n-propanol, n-butanol, n-pentanol, and n-hexanol. The results showed the influence of the alkyl chain length of the n-alkanol on the permselectivity properties of the pervaporation technique in the breakdown of the microemulsions. The variations of the total flux rate J and the enrichment factor β were in parallel with the effect of the cosurfactant on the swelling extent of the PDMS membrane

Use of inverse gas chromatography to account for the pervaporation performance in the microemulsion breakdown

Mass transfer phenomenon that occurs in the pervaporation process when applied to the microemulsion breakdown, was confirmed by the results of inverse gas chromatography. The stationary phase for this study was polydimethylsiloxane (PDMS), a hydrophobic polymer employed as a membrane in the pervaporation technique. The retention times of the different molecule probes (toluene, cyclohexane, and n-butanol) gave an insight into the extent of the interactions between each of these molecules and the stationary phase; these molecules were the components of the two microemulsions in study. The infinite dilution conditions allowed to determine the thermodynamic and the chromatographic parameters γ∞ (the infinite dilution activity coefficient), the Flory-Huggins parameter interactions χ∞12, and V0g (the specific retention volume), respectively. The magnitudes of the latter parameters threw some light on the permselectivity of the membrane in the pervaporation operation

Effect of the Nature of Surfactant on the Reactivity of C,N-diphenylnitrone towards Acrylonitrile in Different Microemulsions Systems

The present work provides an insight into the effect of the nature of surfactant (cationic, anionic), a component of water- and oil-borne microemulsions, on the reaction rate of 1,3-dipolar cycloaddition of C,N-diphenylnitrone with acrylonitrile. The electrostatically attractive character of the cationic surfactant, would bring the reactants closer to each other; hence, a rate enhancement would ensue, particularly within the water-rich zone. Besides the fact that acrylonitrile played a dual role, as a component of the microemulsion and a dipolarphile in the cycloaddition reaction, made the work-up advantageously sound. Additionally, the increase in reagents molar ratio was found to promote higher reactivity

Polyacrylamide-Based Sorbents for the Removal of Hazardous Metals

International audienc

Synthesis of polyacrylamide-bound hydroquinone via a homolytic pathway: Application to the removal of heavy metals

International audienc

Effect of Grafted Hydroquinone on the Acid-Base Properties of Poly(acrylic acid) in the Presence of Copper (II)

International audienc

Kinetic and equilibrium studies of lead(II) adsorption from aqueous media by KIT-6 mesoporous silica functionalized with –COOH

International audienc

Thionation of Essential Oils from Algerian Artemisia Herba-alba L. and Ruta Montana L.: Impact on their Antimicrobial and Insecticidal Activities

Essential oils were extracted from Artemisia herba-alba L. and Ruta montana L. by means of steam distillation and thionated with a reagent combination of phosphorus pentasulfide and sodium bicarbonate. Both parent essential oils and their modified ones were screened for their biological and insecticidal activities. The results showed that essential oils were composed mainly of ketones; essential oils from Artemisia herba-alba L. and those from Ruta montana L. consisted of bicyclic monoterpenes and acyclic aliphatic ketones (thujone, camphor and 2-undecanone), respectively. The antimicrobial activity of essential oils was substantially improved upon thionation (from 10 to 34 mm and from 11 to 32 mm). The insecticidal effect of the thionated essential oil from Ruta montana L. was observed to be very significant, but that of the essential oil from Artemisia herba-alba L. was observed to decrease (from 100% to 70% after 24 hrs. The extracted essential oils as well as their thionated forms were characterized by GC-MS, FT-IR, and UV-visible