Search results for "PLASTICS"
showing 10 items of 2724 documents
Effective copolymerization of ethylene with α,ω-alkenols and homopolymerization of α,ω-alkenols catalyzed by aminophenolate zirconium complex
2019
Abstract A zirconium complex of diamine-bis(phenolate) ligand, [(tBu2O2NN’)ZrCl]2(μ-O) where (tBu2O2NN’) = Me2N(CH2)2N(CH2–2-O−-3,5-tBu2-C6H2)2, activated with (iBu)3Al/Ph3CB(C6F5)4, was for the first time used in copolymerization of ethylene with unsaturated alcohols (CH2 = CH(CH2)nCH2OH, where n = 7, 8, 3). The hydroxyl groups of comonomers were protected with R3-xAlClx (where x = 0 or 1, R = iBu, Et). In contrast to the formerly reported catalysts, the activity of this catalyst is much higher in ethylene/alkenols copolymerization than in ethylene homopolymerization and its lifetime is long. Moreover, the copolymers with high polar comonomer contents (up to 16.4 mol%, 52.3 wt%) were produ…
Organometallic vanadium‐based heterogeneous catalysts for ethylene polymerization. Study of the deactivation process
1998
Slurry polymerizations of ethylene over vanadium catalysts (based on VCl4 and VOCl3) and their MgCl2(THF)2-supported equivalents were studied. Unsupported vanadium catalysts were found to be unstable while the vanadium active sites deposited on the MgCl2(THF)2 complex are stable. A sharply outlined correlation was found between the concentration of vanadium(III) and catalyst productivity. The high activity and stability of the vanadium catalyst when supported on the magnesium complex is attributed to the increase of resistance to reduction of active vanadium(III) to inactive vanadium(II) by an organoaluminium co-catalyst.
“Functional Poly(ethylene glycol)”: PEG-Based Random Copolymers with 1,2-Diol Side Chains and Terminal Amino Functionality
2010
A series of poly(ethylene glycol-co-isopropylidene glyceryl glycidyl ether) (P(EO-co-IGG)) random copolymers with different fractions of 1,2-isopropylidene glyceryl glycidyl ether (IGG) units was synthesized. After acidic hydrolysis a new type of "functional PEGs", namely poly(ethylene glycol-co-glyceryl glycerol) (P(EO-co-GG)) was obtained. Using an initiator that releases a terminal amino moiety after deprotection, functional end groups with orthogonal reactivity to the in-chain groups were obtained. All polymers showed narrow molecular weight distributions (1.07-1.19), and control of the molecular weights was achieved in the range 5000-30 000 g/mol. Random incorporation of both comonomer…
Homopolymerization of styrenic monomers and their copolymerization with ethylene using group 4 non‐metallocene catalysts
2020
Homopolymerization of styrenic monomers (St, p ‐Me‐St, p ‐t Bu‐St, p ‐t BuO‐St) and their copolymerization with ethylene, with the use of [( t Bu2O2NN′)ZrCl]2(μ‐O) (1 ) and ( t Bu2O2NN′)TiCl2 (2 ), where t Bu2O2NN′ = Me2N(CH2)2N(CH2‐2‐O−‐3,5‐t Bu2‐C6H2)2, is explored in the presence of MMAO and (i Bu)3Al/Ph3CB(C6F5)4. The ethylene/styrenic monomers copolymerization with 1 /MMAO produces exclusively copolymers with high activity and good comonomer incorporation whereas the other catalytic systems yield mixtures of copolymers and homopolymers. The use of p ‐alkyl styrene derivatives instead of styrene raises the catalytic activity, comonomer incorporation and molecular weights of the copolyme…
The role of crystalline, mobile amorphous and rigid amorphous fractions in the performance of recycled poly (ethylene terephthalate) (PET)
2012
[EN] The action of thermo-mechanical degradation induced by mechanical recycling of poly(ethylene terephthalate) was simulated by successive injection moulding cycles. Degradation reactions provoked chain scissions and a reduction in molar mass mainly driven by the reduction of diethyleneglycol to ethylene glycol units in the flexible domain of the PET backbone, and the formation of -OH terminated species with shorter chain length. The consequent microstructural changes were quantified taking into account a three-fraction model involving crystalline, mobile amorphous (MAF) and rigid amorphous fractions (RAF). A remarkable increase of RAF, to a detriment of MAF was observed, while the percen…
Modelling of phase transitions and residual thermal stress of CTBN rubber modified epoxy resins during a pultrusion process
2007
Abstract The implicit finite difference and fourth order Runge-Kutta method are used both to solve the heat transfer problem in the pultrusion reaction and to calculate the temperature and conversion distributions within a thermoset composite profile. The aim of our work is to study the influence of a rubbery phase added to the epoxy matrix in production conditions. The results have shown that the rubber modified systems have a low exothermic temperature peak value, so that neither the amount of cured resin nor the final product properties are limited. First of all we will show that the phase transition (gelation and vitrification) zones within the die change as the amount of rubber varies …
Microflow Technology in Polymer Synthesis
2012
Microflow technology, i.e., the use of microfluidic devices for continuous flow synthesis, represents a highly useful and increasingly popular method in organic chemistry. Recently, also an increasing number of polymer synthesis protocols attain benefit from this technique. In particular, the control of highly exothermic, fast polymerization reactions can be improved due to the excellent heat and mass transfer within the small dimensions of the microreactors. Continuous flow setups with different micromixer geometries and flow patterns are currently used for the preparation of a variety of macromolecular architectures by ionic and (controlled) radical polymerization techniques. This Perspec…
Recycling of a starch-based biodegradable polymer
2002
A new starch-based polymeric system, ZI1OU from Novamont, mainly composed of starch and polycaprolactone, was reprocessed several times in an extruder to investigate the recyclability of this biodegradable polymer. A previous investigation of the thermomechanical degradation in a mixer has been also done. The degradation is mostly due to the thermal stress but the presence of the mechanical stress strongly increases the degradation kinetic. During melt processing two concurrent processes take place: the first is the degradation, i.e. the breaking and shortening of polymeric chains, mostly occurring in the PCL phase; the second is the formation of some crosslinked structure in the starch pha…
Processing and mechanical properties of organic filer-polypropylene composites
2005
The addition of organic fillers into thermoplastic polymers is an interesting issue, which has had growing consideration and experimentation during the last years. It can give rise to several advantages. First, the cost of these fillers is usually very low. Also, the organic fillers are biodegradable (thus contributing to an improved environmental impact), and finally, some mechanical and thermomechanical properties can be enhanced. In this study, the effect of the addition of different organic fillers on the mechanical properties and processability of an extrusion-grade polypropylene were investigated. The organic fillers came from natural sources (wood, kenaf, and sago) and were compared …
Methods for Determining the Thermal Transfer in Phase-Changing Materials (PCMs).
2020
A very important issue that needs to be solved as simply and correctly as possible is how to establish the thermal performance of phase-changing materials (PCM). The undertaken researches have analyzed the values of the thermal performances of the PCM taking into account the method of finite elements and the experimental research, respectively, based on a modern measurement system that was designed and implemented. Butyl stearate which has been encapsulated through complex coacervation in polymethyl methacrylate has been used as a PCM. Samples were made containing 10%, 20%, 30% and 40% PCM, respectively, within their structure. The research has established that at both the hot plate and the…