Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

OPYRIGHT

Fig. 58 Rod-bundle phase formed by compounds 184 and 185 with two branched and semiperfluorinated lateral chains and their organization in the LC rod-bundle phases the local cross-section of the columns is thought to be elliptical, but circular when averaged over time and space, hence leading to 2D hexagonal symmetry [342, 343], Reproduced with permission [342], opyright 2008, American Chemical Society (ACS)... Fig. 58 Rod-bundle phase formed by compounds 184 and 185 with two branched and semiperfluorinated lateral chains and their organization in the LC rod-bundle phases the local cross-section of the columns is thought to be elliptical, but circular when averaged over time and space, hence leading to 2D hexagonal symmetry [342, 343], Reproduced with permission [342], opyright 2008, American Chemical Society (ACS)...
Protection was determined as described in Table 11. S026-B is from T4 lysozyme, P is from BPTl, (iNCT-pl and Fos-pl are leucine zippers Ac, acetyl. Histidines were ignored in determining net charge. Adapted from Randall (1992). C opyright 1992 by the AAAS. [Pg.179]

ADVANCKS IN Ql ANTl M CHEMISTRY. VOl.l ME 37 ( opyright 02001 by Academic Press. All righls of reproduction in any form rc.served. [Pg.335]

Figure 19. Pore size distribution of a) aerogel catalyst A(t6 and b) aerogel catalyst AG7. Reprinted from Catithsis Communications. Vol 3. Orlovic el al. Pages 119-123. C opyright (2( 02). with permission from Elsev ier. Figure 19. Pore size distribution of a) aerogel catalyst A(t6 and b) aerogel catalyst AG7. Reprinted from Catithsis Communications. Vol 3. Orlovic el al. Pages 119-123. C opyright (2( 02). with permission from Elsev ier.
Digital Engineering Library McGraw-Hill (www.digitalengineeringlibrary.com) opyright 2006 The McGraw-Hill Companies. All rights reserved. [Pg.541]

Figure 3.14. Simulated CPC of the F+LMWL system where the polymer has the same p, with different poly-molecularity (sp is the spinodal, eir-cles are the critical points, u) o ifu present hypothetical mixtures of two polymers with the exponential MWD) (Koniiigsveld, 1968) [Reprinted from Advances in ( olloid and Interface Science 2 (1968) 151-215. ( opyright 1968 with kind permis-.sion of Elsevier Science NL, Sara Ourgerhart-... Figure 3.14. Simulated CPC of the F+LMWL system where the polymer has the same p, with different poly-molecularity (sp is the spinodal, eir-cles are the critical points, u) o ifu present hypothetical mixtures of two polymers with the exponential MWD) (Koniiigsveld, 1968) [Reprinted from Advances in ( olloid and Interface Science 2 (1968) 151-215. ( opyright 1968 with kind permis-.sion of Elsevier Science NL, Sara Ourgerhart-...
Figure 5.3J. A P-irreducible diagram without (a) and with (6) a P-irreducible insertion (des Cloizeaux, 1981) [Reprinted with permission from J. des Cloizcaiix.. 1. dc Phys. 42 (1981) 63.5-6.52. (, opyright 1981 by KDP Sciences)... Figure 5.3J. A P-irreducible diagram without (a) and with (6) a P-irreducible insertion (des Cloizeaux, 1981) [Reprinted with permission from J. des Cloizcaiix.. 1. dc Phys. 42 (1981) 63.5-6.52. (, opyright 1981 by KDP Sciences)...
Figure 5.45. Tlie tricritical stale region on the state diagram. The solid lino is the pha.se coexistence curve at S —> oo. Inside it is the dashed line, the biiiodal for finite. S (I)uplantier, 1982) [Reprinted with permission from B.Duplantier. J. de Phys. 43 (1982) 991-1019. ( opyright 1982 by EDP Sciences]... Figure 5.45. Tlie tricritical stale region on the state diagram. The solid lino is the pha.se coexistence curve at S —> oo. Inside it is the dashed line, the biiiodal for finite. S (I)uplantier, 1982) [Reprinted with permission from B.Duplantier. J. de Phys. 43 (1982) 991-1019. ( opyright 1982 by EDP Sciences]...
XX = Preferred, f opyright 1996PennWell Corporation. Reproduced by Permission.)... [Pg.212]

Copyright 2000 Marcel Dekker, l oPyright 2000 by Marcel Dekker, Inc. All Rights Reserved. [Pg.1010]


See other pages where OPYRIGHT is mentioned: [Pg.405]    [Pg.78]    [Pg.78]    [Pg.2]    [Pg.1]    [Pg.173]    [Pg.139]    [Pg.347]    [Pg.403]    [Pg.433]    [Pg.375]    [Pg.6]    [Pg.21]    [Pg.568]    [Pg.441]   


SEARCH



All rights reserved opyright International Society of Automation Provided by IHS under license with ISA LicenseeFermilab Research Alliance LLC

Edited by Douglas C. Neckers, David H Volman, Gunther Von Bunau opyright

Edited by Zvi Rappoport opyright

Name Reactions for Carbocyclic Ring Formations Edited by Jie Jack Li opyright

Name Reactions in Heterocyclic Chemistry II Edited by Jie Jack Li opyright

National Institute of Standards and Technology not subject to copyright in the United States opyright

Organocopper Chemistry. Edited by Norbert Krause opyright

Solvent-free organic Synthesis. Kiochi Tanaka opyright

Stuart A. Rice opyright

Unless otherwise noted, all content on this page is Cengage Learning opyright

© 2024 chempedia.info