1997
DOI: 10.1002/(sici)1099-0488(19970930)35:13<2029::aid-polb4>3.0.co;2-r
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Acrylic acid polymerization kinetics

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Cited by 107 publications

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“…The faster rates for the 20 and 40 wt% experiments occur from the start of the polymerization, as seen by the initial rates of conversion in Figure . These results are in agreement with the previous AM and AA batch homopolymerization studies, and are indicative of an apparent reaction order with respect to monomer of greater than unity. The expected rate of monomer conversion ( x ) for FRP in a batch reactor is: dxdt=knormalp(1x)2fknormald[I]knormalt assuming the reaction is first order with respect to monomer concentration and also with respect to radical concentration.…”
Section: Results
supporting
confidence: 92%
How this paper cites the one you are viewing
“…The faster rates for the 20 and 40 wt% experiments occur from the start of the polymerization, as seen by the initial rates of conversion in Figure . These results are in agreement with the previous AM and AA batch homopolymerization studies, and are indicative of an apparent reaction order with respect to monomer of greater than unity. The expected rate of monomer conversion ( x ) for FRP in a batch reactor is: dxdt=knormalp(1x)2fknormald[I]knormalt assuming the reaction is first order with respect to monomer concentration and also with respect to radical concentration.…”
Section: Results
supporting
confidence: 92%
How this paper cites the one you are viewing
“…This result is consistent with an 1 / 2 -order with respect to the initial initiator concentration. This behavior was expected and is in good agreement with the literature. …”
Section: Results
supporting
confidence: 92%
“…From the highest part of their Arrhenius plot, one can calculate an E r of about 49.5 kJ mol −1 , which is closer to our measured E r . On the other hand, Cutié et al obtained E r of about 40.1 kJ mol −1 , within a temperature range above the curvature limit observed on the graph published by Scott and Peppas, up to 85 °C . Scott and Peppas used a lower concentration than we did, i.e.…”
Section: Results
supporting
confidence: 69%
How this paper cites the one you are viewing
“…After the same inhibition period (around 1h), the polymerization rate strongly decreased when the pH was increased from 1.8 to 5.0, but increased again for pH = 7.0 remaining, however, lower than in the case of pH = 1.8 but faster than when pH = 4.0. These results are consistent with observations already made for the free radical polymerization of AA in water 26,27 and the same conclusions on the impact of pH on kp may apply when RAFT is employed. The examination of the ASEC peaks evolution versus conversion gives additional information on the control of the RAFT process (Figure 3).…”
Section: Raft Synthesis Of Paa In Water
supporting
confidence: 92%