Copper(0)-mediated radical polymerisation in a self-generating biphasic system

Herein, we demonstrate the synthesis of well-defined poly(n-alkyl acrylate)s via copper(0)-mediated radical polymerisation in a self-generating biphasic system. During the polymerisation of n-butyl acrylate in DMSO, the polymer phase separates to yield a polymer-rich layer with very low copper content (ICP-MS analysis: 0.016 wt%). The poly(n-butyl acrylate) has been characterized by a range of techniques, including GPC, NMR and MALDI-TOF, to confirm both the controlled character of the polymerisation and the end group fidelity. Moreover, we have successfully chain extended poly(n-butyl acrylate) in this biphasic system several times with n-butyl acrylate to high conversion without intermediate purification steps. A range of other alkyl acrylates have been investigated and the control over the polymerisation is lost as the hydrophobicity of the polymer increases due to the increase in alkyl chain length indicating that it is important for the monomer to be soluble in the polar solvent

Graft Copolymerization of Methacrylic Acid, Acrylic Acid and Methyl Acrylate onto Styrene–Butadiene Block Copolymer

Methyl acrylate, methacrylic acid, and acrylic acid have been graft copolymerized onto styrene–butadiene block copolymer. All three monomers react through the macroradical interacting with the double bond of butadiene. The site of reaction has been established by infrared spectroscopy. For methyl acrylate every unit of the styrene–butadiene block copolymer is grafted but only a small fraction is grafted when the acids are used. The difference apparently lies in the fact that the reaction with the ester is homogeneous while with the acids the reactions are heterogeneous

Sequential curing of thiol-acetoacetate-acrylate thermosets by latent Michael addition reactions

Thiol-acetoacetate-acrylate ternary dual-curing thermosets were prepared by a sequential process consisting of thiol-Michael addition to acrylates at room temperature followed by Michael addition of acetoacetates to acrylates at moderately elevated temperature. The curing sequence can be controlled with the help of the different acidities of the protons on thiol and acetoacetate groups, the favorable pKa of the base used as catalyst and the self-limiting character of Michael additions. The latency of the curing steps can be regulated by selection of the right catalysts, temperature and curing conditions. The properties of the intermediate and final materials can be tuned by changing the structure of the monomers and the contribution of both Michael addition reactions.Postprint (author's final draft

Ablative resin Patent

Ablative resins used for retarding regression in ablative materia

Sequential curing of amine-acrylate-methacrylate mixtures based on selective aza-Michael addition followed by radical photopolymerization

Dual curing systems find various uses in industry with the process flexibility they provide which allows tailoring properties at different curing stages in accordance with application requirements. A safe and efficient dual curing scheme is proposed here for a set of mixtures containing different proportions of acrylates and methacrylates. The first curing stage is a stoichiometric aza-Michael addition between acrylates and an amine, followed by photo-initiated radical homopolymerization of methacrylates and remaining acrylates. An analysis of aza-Michael reaction kinetics confirmed that amines react selectively with acrylates, leaving methacrylates unreacted after the first curing stage. It was found that acrylate-rich mixtures achieve complete global conversion at the end of the scheme. However, the highest crosslinking density and thermal resistance was observed in a methacrylate-rich formulation. The resulting materials show a wide range of viscoelastic properties at both curing stages that can be tailored to a variety of industrial application needs.Postprint (author's final draft

Candida antarctica lipase-catalyzed synthesis and characterization of novel acrylic teroligomers

The synthesis of three novel low molecular weight acrylic terpolymers, containing at random sequences of ethyl acrylate, acrylic acid and N-(2-hydroxyethyl)acrylamide, catalyzed by Candida antarctica lipase was successfully conducted in organic media. For the first time, these products have been enzymatically synthesized using ethyl acrylate as the only monomer starting material and taking advantage of a triple activity displayed by the lipase. In the presence of ethanolamine, the enzyme not only catalyzes the chain polymerization of ethyl acrylate but also the aminolysis and hydrolysis of the pendant ester groups affording the terpolymers. The products were characterized by 1H and 13C NMR and UV-MALDI-TOF-MS.Fil: Baldessari, Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis y Métodos Físicos en Química Orgánica. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Unidad de Microanálisis y Métodos Físicos en Química Orgánica; ArgentinaFil: Fatema, M. Kaniz. Ehime University; JapónFil: Nonami, Hiroshi. Ehime University; JapónFil: Erra Balsells, Rosa. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; ArgentinaFil: Rustoy, Eduardo Miguel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis y Métodos Físicos en Química Orgánica. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Unidad de Microanálisis y Métodos Físicos en Química Orgánica; Argentin

Redundancy of reinforced glass beams : temperature, moisture and time dependent behaviour of the adhesive bond

The most important aspect of the reinforced glass beam concept, which provides ductility and redundancy for structural glass beams, is the adhesive bond between glass and reinforcement. To guarantee structural safety, this adhesive bond has to service under all conditions. The effects of elevated temperature, moisture exposure and load duration on the adhesive bond, have separately been investigated through three series of bending tests on 1.5 m reinforced glass beam specimens. A first series has been tested at 60 C; a second series has been tested after 8 weeks of salt-water-spraying; and a third series has been loaded until initial failure whereupon it has been left statically loaded for at least 72 hours. The results show that the reinforced glass beam concept is a redundant system which shows, dependent on the applied adhesive, a significant residual strength even at extreme temperature and moisture conditions, and for a significant period of time

Combined experimental and computational investigations of rhodium-catalysed C-H functionalisation of pyrazoles with alkenes

Detailed experimental and computational studies have been carried out on the oxidative coupling of the alkenes C(2)H(3)Y (Y=CO(2)Me (a), Ph (b), C(O)Me (c)) with 3-aryl-5-R-pyrazoles (R=Me (1 a), Ph (1 b), CF(3) (1 c)) using a [Rh(MeCN)(3)Cp*][PF(6)](2)/Cu(OAc)(2)⋅H(2)O catalyst system. In the reaction of methyl acrylate with 1 a, up to five products (2 aa–6 aa) were formed, including the trans monovinyl product, either complexed within a novel Cu(I) dimer (2 aa) or as the free species (3 aa), and a divinyl species (6 aa); both 3 aa and 6 aa underwent cyclisation by an aza-Michael reaction to give fused heterocycles 4 aa and 5 aa, respectively. With styrene, only trans mono- and divinylation products were observed, whereas with methyl vinyl ketone, a stronger Michael acceptor, only cyclised oxidative coupling products were formed. Density functional theory calculations were performed to characterise the different migratory insertion and β-H transfer steps implicated in the reactions of 1 a with methyl acrylate and styrene. The calculations showed a clear kinetic preference for 2,1-insertion and the formation of trans vinyl products, consistent with the experimental results

Ultraviolet-curable Silicone/Urethane Elastomer and Its Selective Modulus Enhancement

Department of Chemical EngineeringThermosets usually have brittle structure, but thermosetting polyurethane (PU) is classified as elastomer due to its urethane linkage in the backbone. Polyurethanes are used in many areas in a form of foam, adhesive and especially as an elastomer. To utilize elastomers in various applications without being fractured, various methods to control the mechanical properties of elastomers have been investigated such as incorporating fillers and additives or creating multiple networks. In this study, ultraviolet-curable silicone containing polyurethane acrylate was synthesized from poly(tetrahydrofuran) (PTH), hydroxy-terminated poly(dimethyl siloxane) (PDMS) and isophorone diisocyanate. The polyurethane chain was terminated with acrylate to fabricate modulus tunable and rapidly crosslinkable silicone/urethane composite elastomer. By adding 3-(trimethoxysilyl)propyl acrylate to the silicone/urethane elastomer network, the mechanical properties of silicone/urethane elastomer can be enhanced by creating additional covalent bonds at elevated temperature. The mechanical properties of the silicone-contained PUA elastomer can be enhanced even after complete photopolymerization, and local modulus enhancement is also possible by heating only desired area of the elastomer. We believe that the silicone/urethane elastomer can be used to fabricate flexible devices, force sensor, etc.clos