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Diamond domain

The effect of the substrate temperature can also be considered (Fig. 16c). As the substrate temperature iacreases, the triangular diamond domain region ia the C—H—O equiUbrium diagram shrinks to almost aline at the highest temperature. [Pg.219]

Figure 4 Atomic C-H-O diamond deposition phase diagram with the diamond domain. The diagram comprises deposition experiments from over 25 references [24]. (Reproduced from Diamond and Related Materials, 1, Bachmann, R K., et al. Towards a general concept of diamond chemical vapor deposition, pp. 1—12. Copyright 1991, with permission from Elsevier Science.)... Figure 4 Atomic C-H-O diamond deposition phase diagram with the diamond domain. The diagram comprises deposition experiments from over 25 references [24]. (Reproduced from Diamond and Related Materials, 1, Bachmann, R K., et al. Towards a general concept of diamond chemical vapor deposition, pp. 1—12. Copyright 1991, with permission from Elsevier Science.)...
Fig. 10 PEO melting temperatures vs. inverse PEO domain size as a function of block architecture (squares, PS-6-PI-6-PEO diamonds PI-6-PS-6-PEO). PI poly(isoprene) w is given in angstroms. (Reprinted with permission from [121]. Copyright 2003 American Chemical Society)... [Pg.50]

Fig. 4.6 High resolution electron micrograph of natural goethite a) Diamond-shaped cross sections of domains running along [010] and bounded by 101 faces. Lattice fringes correspond to the c -parameter. b) Higher magnification shows the a fringes (ca. 1 nm) and structural distortions. (Smith Eggleton, 1983 with permission courtesy R.A. Eggleton). Fig. 4.6 High resolution electron micrograph of natural goethite a) Diamond-shaped cross sections of domains running along [010] and bounded by 101 faces. Lattice fringes correspond to the c -parameter. b) Higher magnification shows the a fringes (ca. 1 nm) and structural distortions. (Smith Eggleton, 1983 with permission courtesy R.A. Eggleton).
Fig. 12.17 Dissolution morphology of synthetic 210 faces, c) Monodomainic Al-goethite (Al/ goethite crystals after partial dissolution in 6 M (Fe-tAI) = 0.097 mol mol" ) with cavernous dis-HCI at 25 °C. a) Pure goethite with dissolution solution at crystal edges (Schwertmann, 1984 a, along domain boundaries, b) Pure goethite with with permission), diamond-shaped dissolution holes bounded by... Fig. 12.17 Dissolution morphology of synthetic 210 faces, c) Monodomainic Al-goethite (Al/ goethite crystals after partial dissolution in 6 M (Fe-tAI) = 0.097 mol mol" ) with cavernous dis-HCI at 25 °C. a) Pure goethite with dissolution solution at crystal edges (Schwertmann, 1984 a, along domain boundaries, b) Pure goethite with with permission), diamond-shaped dissolution holes bounded by...
Figure 11. Dependence of the volume fractions of oil (open symbols) and alcohol (filled symbols) in a bicontinuous micro-emulsion as a function of the mole fraction of alcohol in the water phase. The different symbols refer to different volume fractions of oil and water domains in the microemulsion = 0.25 (circles), 0.45 (squares), 0.55 (triangles), and 0.75 (diamonds). The system consists of SDS, 1-pentanol, cyclohexane, water, and 0.3M NaCl. Figure 11. Dependence of the volume fractions of oil (open symbols) and alcohol (filled symbols) in a bicontinuous micro-emulsion as a function of the mole fraction of alcohol in the water phase. The different symbols refer to different volume fractions of oil and water domains in the microemulsion <I> = 0.25 (circles), 0.45 (squares), 0.55 (triangles), and 0.75 (diamonds). The system consists of SDS, 1-pentanol, cyclohexane, water, and 0.3M NaCl.
Diamond, M. S., Garcia-Aguilar, J., Bickford, J. K., Corbi, A. L., and Springer, T. A. (1993). The I domain is a major recognition site on the leukocyte integrin Mac-1 (CDllb/CD18) for four distinct adhesion ligands. J. Cell. Biol. 120, 1031-1043. [Pg.58]

Fig. 5. Platform sequence alignments of the MHC class I-like ligands of NKG2D. Sequences of MIC-A and -B, the ULBPs and the RAE-ls have been aligned, divided by family and domain, using CLUSTALW (Thompson et al, 1994). Note that the alignments across families are only very approximate at these levels of sequence identity. Sequences have been numbered from the initiator methionine in the leader peptide, but only the residues in the mature proteins have been shown. Cysteines have been highlighted, and disulhde bond partners have been indicated with matching symbols (, f). For the MIC sequences, allelic substitutions have been indicated by the additional residues shown below the sequences (deletions are indicated with an X ). Diamonds below the sequences indicate NKC2D contact positions, based on the known complex structures (MIC-A 001, ULBPS, and RAE-1/5). Fig. 5. Platform sequence alignments of the MHC class I-like ligands of NKG2D. Sequences of MIC-A and -B, the ULBPs and the RAE-ls have been aligned, divided by family and domain, using CLUSTALW (Thompson et al, 1994). Note that the alignments across families are only very approximate at these levels of sequence identity. Sequences have been numbered from the initiator methionine in the leader peptide, but only the residues in the mature proteins have been shown. Cysteines have been highlighted, and disulhde bond partners have been indicated with matching symbols (, f). For the MIC sequences, allelic substitutions have been indicated by the additional residues shown below the sequences (deletions are indicated with an X ). Diamonds below the sequences indicate NKC2D contact positions, based on the known complex structures (MIC-A 001, ULBPS, and RAE-1/5).

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