Bis(pyrrolide-imine) Ti complexes in conjunction with methylalumoxane (MAO) were found to work as efficient catalysts for the copolymerization of ethylene and norbornene to afford unique copolymers via an addition-type polymerization mechanism. The catalysts exhibited very high norbornene incorporation, superior to that obtained with Me(2)Si(Me(4)Cp)(N-tert-Bu)TiCl(2) (CGC). The sterically open and highly electrophilic nature of the catalysts is probably responsible for the excellent norbornene incorporation. The catalysts displayed a marked tendency to produce alternating copolymers, which have stereoirregular structures despite the C(2) symmetric nature of the catalysts. The norbornene/ethylene molar ratio in the polymerization medium had a profound influence on the molecular weight distribution of the resulting copolymer. At norbornene/ethylene ratios larger than ca. 1, the catalysts mediated room-temperature living copolymerization of ethylene and norbornene to form high molecular weight monodisperse copolymers (M(n) > 500,000, M(w)/M(n) < 1.20). (13)C NMR spectroscopic analysis of a copolymer, produced under conditions that gave low molecular weight, demonstrated that the copolymerization is initiated by norbornene insertion and that the catalyst mostly exists as a norbornene-last-inserted species under living conditions. Polymerization behavior coupled with DFT calculations suggested that the highly controlled living polymerization stems from the fact that the catalysts possess high affinity and high incorporation ability for norbornene as well as the characteristics of a living ethylene polymerization though under limited conditions (M(n) 225,000, M(w)/M(n) 1.15, 10-s polymerization, 25 degrees C). With the catalyst, unique block copolymers [i.e., poly(ethylene-co-norbornene)(1)-b-poly(ethylene-co-norbornene)(2), PE-b-poly(ethylene-co-norbornene)] were successfully synthesized from ethylene and norbornene. Transmission electron microscopy (TEM) indicated that the PE-b-poly(ethylene-co-norbornene) possesses high potential as a new material consisting of crystalline and amorphous segments which are chemically linked.
Novel poly(ethylene glycol) (PEG) derivatives having pendant amino groups were prepared by copolymerization of allyl glycidyl ether with ethylene oxide followed by chemical modification of the double bond side chains. Dropwise addition of the mixture of monomers to the anionic initiator gave an almost monodisperse (Mw/Mn = 1.05) random copolymer. 1H NMR spectra showed that addition of 2-aminoethanethiol to the pendant allyl groups of the copolymer was completely carried out in methanol without catalyst, and an aminated PEG derivative with a definite structure was obtained. Acetylation of the pendant amino groups was readily performed by acetic anhydride with triethylamine. A gel permeation chromatogram of the acetylated polymer showed a very narrow molecular weight distribution (Mw/Mn = 1.06) of the polyamine. These cationic PEG derivatives make amphiphilic polyion complexes with fatty acids, and then aggregate in water. A fluorescence study using pyrene as a microenvironment probe revealed that the aminated PEG-lauric acid ion complex could take up the hydrophobic fluorescence probe into the lipophilic field inside, and they also had a critical aggregation concentration at [lauric acid] = 0.7 mM. It is much lower than the critical micelle concentration of the corresponding fatty acid sodium salts, indicating high stability of the polymer-fatty acid aggregate.
The physical processes and chemical reactions that take place inside different temperature plasma zones in water are only partially understood. The present study uses the emission spectroscopy and hydrogen peroxide measurements as indicators of the processes that take place on the gas-liquid boundary and inside plasma. Based on the hydrogen peroxide measurements with negative and positive high-voltage polarities as a function of solution conductivity, it was concluded that the main difference between positive polarity plasma and negative polarity plasma lies in the active radical concentration inside plasma. Data suggested that in the positive polarity electrical discharge the hydrogen peroxide concentration depends on the solution pH, whereas in the negative polarity discharge, it depends on the solution conductivity. Also, only in the negative polarity discharge do some of the electrons that are emitted from the high voltage electrode diffuse into the bulk where they react with the solutes.
We studied the oxidative coupling and reforming of CH 4 with CO 2 to C 2 H 4 , CO, and H 2 using a pulsed plasma with a pulse frequency ranging from 166 to 3050 PPS. The largest selectivity of C 2 H 4 was 64% with 31% CH 4 conversion and 24% CO 2 conversion at 2920 PPS and 500 °C. Selectivities of CO and H 2 were about 20% and 100%, respectively. Ratios of H 2 to CO and (CO + CO 2 ) were, respectively, 7.1 and 2.5, which are acceptable for methanol production from (CO + H 2 ) and (CO 2 + H 2 ) over a catalyst. The results indicated that the pulsed plasma with a high frequency can promote conversion of CH 4 and CO 2 . The energy efficiency of the pulsed plasma was improved using a high pulse frequency and a high reaction temperature. We suggested that a pulsed plasma with a high pulse frequency is useful for oxidative coupling and reforming of CH 4 with CO 2 in industry.
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