Sublimation of NH4Cl was used to transfer gallium to the vapor phase and it was then reacted with NH3.
The MWNT-NH2 was then reacted with PMMA through the aid of amino groups to form MWNT-NH2/PMMA nanocomposites.
After tosylating PCL-diol with p-toluenesulfonylchloride (TsCl), tosylated poly(caprolactone) (PCL OTs) was then reacted with hexamethylenediamine (HMD).
The hydroxyl group in UDA was then reacted with butyric anhydride to introduce a larger pendant group that could later inhibit crystallization of its polymer.
A stream containing ethylene and methane was then reacted over gallium-loaded and copper-loaded ZSM-5 to produce higher molecular weight hydrocarbons.
The obtained acrylamide-N,N-dimethylaminopropylmaleimide (ADAPM) copolymer was then reacted with propane sultone to yield a novel acrylamide-N,N-dimethylmaleimidopropylammonium propanesulfonate (ADMMAPS) copolymer.
The styrene-N,N′-dimethylaminopropyl maleimide (SDMAPM) copolymer obtained was then reacted with propane sultone to yield a styrene-[N,N′-dimethyl(maleimidopropyl)ammonium propane sulfonate] (SDMMAPS) copolymer.
An excess of diphenylethylene-capped polystyryllithium (PSLi) was then reacted with the functionalized backbone to yield materials having long chain branches.
The obtained reactive PBZ was then reacted at room temperature with dithiol compounds in CHCl3 CH3OH (1:1, v:v), namely 1,2-ethanedithiol and 1,6-hexanedithiol.
The membrane was then reacted with horseradish-peroxidase conjugated secondary antibodies (Jackson Immunoresearch Labs, West Grove, PA) and enhanced chemiluminescence (ECL) detection was performed according to the manufacturer's instructions (Biological Industries, Beit HaEmek, Israel).
The hydroxy-terminated PLA was then reacted with itaconic anhydride to produce terminal carboxylic acid groups, which were neutralized with appropriate metal acetates to produce Na-, Li-, K-, Zn-, Ca- and Y-ω and α,ω-telechelic PLA ionomers.
