The combination of cellulose nanocrystals (CNCs) and poly(ethylene glycol) methyl ether methacrylate (PEGMA) was evaluated to synthesize stable latexes by surfactant-free emulsion polymerization of methyl methacrylate (MMA). Cellulose-particle interaction was provided due to the dual role of PEGMA, acting as water-soluble comonomer with MMA under emulsion polymerization conditions and able to interact with CNCs -recovered from sulfuric acid hydrolysis (H2SO4-CNCs). After preliminary experiments designed to validate the affinity between CNCs and PEG-stabilized PMMA particles obtained by MMA/PEGMA emulsion copolymerization, the effect of the PEGMA content and molar mass, and also of the content of CNCs on the kinetics of the polymerization and the stability of the latexes were investigated. The use of PEGMA300 (Mn = 300 g mol -1 , 2 to 10 wt%) allowed the formation of a stable latex, however with a broad particle size distribution and the presence of both small (ca. 25 -50 nm) and large (ca. 425 -650 nm) particles (at 10 wt%, Dn = 278 nm and Dw/Dn = 1.34). Increasing the molar mass of PEGMA (PEGMA950 or PEGMA2080) significantly increased the fraction of small particles. This was explained by the nucleation and growth of small polymer particles adsorbed at the CNCs' surface, resulting in a particular organization where the CNCs were covered by several polymer particles. The influence of the initial amount of CNC in these systems was finally evidenced, the polymerization being faster as the content of CNCs increased, but only the latexes prepared with 2 and 5 wt% of CNCs were stable.

Poly(acrylamide-co-acrylic acid) (P(AAm-co-AA)-X) was prepared by RAFT/MADIX and used as hydrophilic macromolecular chain transfer agent (macroCTA) in the aqueous emulsion copolymerization of vinyl acetate (VAc) and ethylene. Stable latexes were...

Commercially available Ni(II) and Co(II) complexes - M(acac)2 (acac=acetylacetonate) and M(tmhd)2 (tmhd = 2,2,6,6-tetramethyl-3,5-heptanedionato) - exhibit catalytic activity for alkene/vinylsilane dehydrogenative silylation (DS) and hydrosilylation (HS) with tertiary silanes without...