Biodegradability of Single and Mixed Surfactant Formulations

Even though detergent surfactants are mandated to be biodegradable, the environmental fate of these surfactants when mixed together in bodies of water is still not established. The study aimed to determine the biodegradability of NaLAS/CTAB surfactant combinations by measuring the amount of evolved CO2 which was measured using the OECD 301b procedure. The 90/10 and 10/90 NaLAS/CTAB systems showed a decline in biodegradation behaviors which were recorded as 55.88% and 40.12% biodegradation, respectively, after a 28-day monitoring period. Conductivity results revealed changes in the availability of ions in the system. An inflection point was observed at a CTAB concentration of 700 ppm. The highest turbidity was noted at a NaLAS/CTAB molar ratio of 1.39:1 which indicated the formation of insoluble catanionic salts in the system. Conductivity and turbidity testing revealed the formation of anionic-cationic structures such as micelles and ion-ion complexes. These structures may alter the natural degradation mechanism of microorganisms, thus leading to the slower rate of biodegradation or incomplete degradation of the surfactants

Nucleophilicity of Neutral versus Cationic Magnesium Silyl Compounds

Charge and ancillary ligands affect the reactivity of monomeric tris(trimethylsilyl)silyl magnesium compounds. Diamine-coordinated (tmeda)Mg{Si(SiMe3)3}Me (tmeda = tetramethylethylenediamine; 2-tmeda) and (dpe)Mg{Si(SiMe3)3}Me (dpe =1,2-N,N-dipyrrolidenylethane; 2-dpe) are synthesized by salt elimination reactions of L2MgMeBr and KSi(SiMe3)3. Compounds 2-tmeda or 2-dpe react with MeI or MeOTf to give MeSi(SiMe3)3 as the product of Si–C bond formation. In contrast, 2-tmeda and 2-dpe undergo exclusively reaction at the magnesium methyl group with electrophiles such as Me3SiI, B(C6F5)3, HB(C6F5)2, and [Ph3C][B(C6F5)4]. These reactions provide a series of neutral, zwitterionic, and cationic magnesium silyl compounds, and from this series we have found that silyl group transfer is less effective with cationic magnesium compounds than neutral complexes