The monomer β‐myrcene, a renewable resource, was polymerized in cyclohexane using two different Ziegler‐Natta catalyst systems based on neodymium Nd(Oi‐Pr)3 and NdV3. The Nd(Oi‐Pr)3 was combined with [HNMe2Ph][B(C6F5)4] (or [CPh3][B(C6F5)4]) and Al(i‐Bu)3 (or Al(i‐Bu)2H). Next, the NdV3 was activated using Al(i‐Bu)3 and AlEt2Cl. Both catalyst systems exhibited high polymer yields near 100 % in the established reaction time, high polymer molecular masses, and broad molecular mass distributions. The catalyst systems gave an effective and stereospecific polymerization reaction of β‐myrcene providing high cis selectivity of 1,4‐polymyrcenes (> 92 %) with a glass transition temperature between −66 and −62 °C. The above‐mentioned features of resulting elastomers in conjunction with the polymer's molecular masses and molecular mass distributions proved to be sensitive to borane and alkylaluminum compounds molar ratios, [B]/[Nd] and [Al]/[Nd] using Nd(Oi‐Pr)3 and [Cl]/[Nd] and [Al]/[Nd] with NdV3.

In this work, we explore the statistical copolymerization of 1,3-butadiene with the terpenic monomers myrcene and farnesene, carried out via coordination polymerization using a neodymium-based ternary catalytic system.

This article proposes a method to produce bio-elastomer nanocomposites, based on polyfarnesene or polymyrcene, reinforced with surface-modified graphene oxide (GO).

The decomposition rate constant (kd) of diethyl ketone triperoxide (DEKTP, 3,3,6,6,9,9‐hexaethyl‐1,2,4,5,7,8‐hexaoxacyclononane) in methyl methacrylate (MMA) was determined by the kinetic study of its thermal decomposition at temperatures from 110 to 140°C. The calculated kd for DEKTP in MMA was 2.4 times lower (at 130°C) compared with that previously determined and reported in styrene (St). Density functional theory (DFT) calculations demonstrated that the decomposition of DEKTP molecule in MMA required higher interaction energy than in St, thus explaining its lower kd value. Bulk polymerization kinetics of MMA using DEKTP as the initiator revealed the presence of an induction period, in contrast with St polymerization, providing clear evidence of the solvation state influence at early polymerization stages. This work provides mechanistic insights into the interactions among the multi‐functional cyclic peroxide DEKTP and vinyl monomers; St and MMA, and their influence on the polymerization kinetics. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 42905.

Considering the current trend of finding sustainable alternatives to the exisitng fossil-based plastics, in this review we describe what makes a bioelastomer to be considered “bio”, and what does this...

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In this communication, γ‐phenyl‐γ‐butyrodithiolactone (DTL1) is presented as the first example of a new type of control agent. The styrene polymerization carried out at 60 °C in the presence of DTL1 exhibits living characteristics, without consuming DTL1 during the process. This unprecedented behavior was explained by a mechanism based on the reversible formation of a persistent radical adduct between the DTL1 and the polystyrene macroradicals.magnified image

Chitosan-coated magnetic nanoparticles (CMNP) were prepared in one-step by precipitation in a high-aqueous phase content reverse microemulsion in the presence of chitosan. The high-aqueous phase concentration led to productivities close to 0.49 g CMNP/100 g microemulsion; much higher than those characteristic of precipitation in reverse microemulsions for preparing magnetic nanoparticles. The obtained nanoparticles present a narrow particle size distribution with an average diameter of 4.5 nm; appearing to be formed of a single crystallite; furthermore they present superparamagnetism and high magnetization values; close to 49 emu/g. Characterization of CMNP suggests that chitosan is present as a non-homogeneous very thin layer; which explains the slight reduction in the magnetization value of CMNP in comparison with that of uncoated magnetic nanoparticles. The prepared nanoparticles show high heavy ion removal capability; as demonstrated by their use in the treatment of Pb 2+ aqueous solutions; from which lead ions were completely removed within 10 min.