Search

A silicate-selective polymer-supported reagent has been developed that utilizes the reactivity of silicate to generate polyanionic Keggin structures. Heptamolybdate and heptatungstate anions are immobilized onto trimethylammonium ligands bound to microporous poly(vinylbenzyl chloride) beads. The heptamolybdate complexes >90% of the silicate from a 20 ppm solution at pH 7; the heptatungstate has a lower affinity, complexing 40% of the silicate. Complexation by the heptamolybdate remains high throughout the pH range 3.8–10.7. Sorption is unaffected by the presence of chloride, sulfate, and nitrate ions. The apparent rate of reaction is maximized by immobilizing the ligand on an expanded gel support: whereas the microporous polymer requires 24 h to complex all of the silicate from a 100 ppm solution, the expanded gel attains that level in 4 h. The rate-limiting step is thus identified as accessibility of the silicate to the heptamolybdate rather than the rate of reaction to form the silicomolybdate. FTIR spectra confirm silicomolybdate formation: The heptamolybdate polymer has four characteristic bands at 715, 845, 912 and 945 cm −1 and these bands get weaker as silicate reacts with the heptamolybdate; at complete reaction, the band at 845 cm −1 disappears. The spectrum of the silica-saturated polymer has strong bands at 900–904 cm −1 and 790–800 cm −1 , consistent with the spectrum of tert-butylammonium silicododecamolybdate.

Membranes that deliver nanoscale size selectivity are desirable for applications ranging from water treatment to molecular separations. Here we describe polymer thin film composite membranes coated with amphiphilic graft copolymers consisting of a poly(vinylidene fluoride) (PVDF) backbone and poly(oxyethylene methacrylate) (POEM) side chains, PVDF-g-POEM. Transmission electron microscopy and thermal analysis reveal that these materials molecularly self-assemble into bicontinuous nanophase domains of semicrystalline PVDF, providing structural integrity, and poly(ethylene oxide) (PEO), providing selective transport channels of defined size. PVDF ultrafiltration membranes coated with PVDF-g-POEM wet instantaneously and reject >99.9% of emulsified oil from a 1000 ppm oleic acid/triethanolamine/water microemulsion feed at 66 psi without fouling. Their molecular sieving capability is demonstrated through separation of like-charged organic dyes varying in molecular dimensions by several angstroms. Thicker films ...

The title compound, synthesized by a carbenoid cyclization-rearrangement route, is the most stable member of the bicyclo[2.1.0]pentane series yet prepared.

2-t-butylbicyclo[3.1.0]hex-1-ene dimerizes primarily by a [σ+ π] way, whereas 2,5-di-t-butylbicyclo[3.1.0]hex-1-ene undergoes an unusual hydrogen shift reaction to 1,3-di-t-butyl-2-methylcyclopentadiene.