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33
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85033172596
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y], where (x + y) = 1. For x = 0.15 and y = 0.85, the calculated N/C × 100 atomic ratio was 6.81 (experimental value = 6.96)
-
y], where (x + y) = 1. For x = 0.15 and y = 0.85, the calculated N/C × 100 atomic ratio was 6.81 (experimental value = 6.96).
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34
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3242816897
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37
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0000538761
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40
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85033180606
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note
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The low percentage of F atoms in the blank means that the residual carbonyl functions of the PEEK-OH (about 15%) are practically unreactive. Indeed, the PEEK carbonyl functions are part of benzophenone motifs. It is well established in organic synthesis that benzophenone is poorly ractive towards nucleophiles (steric effect; stabilization by resonance), and that the formation of Schiff's bases requires acid catalysis.
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41
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85033182527
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-
note
-
z], where (y + z) = 0.85. For y = 0.05 and z = 0.80, the calculated N/C × 100 atomic ratio was 8.77 (experimental value = 8.6). For y = 0.35 and z = 0.45, the calculated F/C × 100 atomic ratio was 5.4 (experimental value = 5.51).
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42
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0001738283
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J. Marchand-Brynaert, M. Deldime, I. Dupont, J.-L. Dewez, and Y.-J. Schneider, J. Colloid Interface Sci., 173, 236 (1995).
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Marchand-Brynaert, J.1
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Schneider, Y.-J.5
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43
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0030002667
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P. Mougenot, M. Koch, I. Dupont, Y.-J Schneider, and J. Marchand-Brynaert, J. Colloid Interface Sci., 177, 162 (1996).
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Mougenot, P.1
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Marchand-Brynaert, J.5
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44
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0030196088
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T. Boxus, M. Deldime-Rubbens, P. Mougenot, Y.-J. Schneider, and J. Marchand-Brynaert, Polym. Adv. Technol., 7, 589 (1996).
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Marchand-Brynaert, J.5
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45
-
-
85033187121
-
-
note
-
z], where (y + z) = 0.85. For y = 0.55 and z = 0.30, the calculated N/C × 100 atomic ratio was 7.56 (experimental value = 7.51).
-
-
-
-
46
-
-
85033159170
-
-
note
-
z], where (y + z) = 0.85. For y = 0.6 and z = 0.25, the calculated N/C × 100 atomic ratio was 8.24 (experimental value = 8.25).
-
-
-
-
49
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0021743024
-
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W. S. Ramsey, W. Hertl, D. E. Nowlan, and N. J. Binkowski, In Vitro, 20, 802 (1984).
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Steele, J.G.5
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