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Scanning electron micrograph of surface

The processes for manufacturing microporous membranes can be broadly divided into wet processes and dry processes. Both processes usually employ one or more orientation steps to impart porosity and/or increase tensile strength. Figure 2 shows scanning electron micrographs of surfaces of separators made by each process. [Pg.555]

Figure 2. Scanning electron micrographs of surfaces of microporous membranes made by wet and dry processes. (a) Setela microporous membrane (net process) (b) Celgard microporous membrane (dry process). Figure 2. Scanning electron micrographs of surfaces of microporous membranes made by wet and dry processes. (a) Setela microporous membrane (net process) (b) Celgard microporous membrane (dry process).
Fig. 4.3 Scanning electron micrographs of surface and cross section for prepared three-dimensionally ordered macroporous Li jLa jjTiOj... Fig. 4.3 Scanning electron micrographs of surface and cross section for prepared three-dimensionally ordered macroporous Li jLa jjTiOj...
Fig. 11 Scanning electron micrographs of surface changes, a after 10 pulses with 30 mj cnT2 at 308 nm and b after 60 pulses with 30 mj cm-2 at 308 nm. REPRINTED WITH PERMISSION OF [Ref. 62], COPYRIGHT (1996) American Chemical Society... Fig. 11 Scanning electron micrographs of surface changes, a after 10 pulses with 30 mj cnT2 at 308 nm and b after 60 pulses with 30 mj cm-2 at 308 nm. REPRINTED WITH PERMISSION OF [Ref. 62], COPYRIGHT (1996) American Chemical Society...
Fig. 3. Scanning electron micrographs of surfaces of specimens after exposure for 50 h at 700°C a) FA 49, environment 1, b) FA 58, environment 1. c) FA 56, environment 1, d) FA 49, preoxidized, environment 2, e) FA 56, environment 2, f) FA 56, preoxidized, environment 2... Fig. 3. Scanning electron micrographs of surfaces of specimens after exposure for 50 h at 700°C a) FA 49, environment 1, b) FA 58, environment 1. c) FA 56, environment 1, d) FA 49, preoxidized, environment 2, e) FA 56, environment 2, f) FA 56, preoxidized, environment 2...
Fig. 9. Scanning electron micrographs of surface and cross-sections of beaded resins obtained by suspension copolymerization of AOTcp with styrene and divinylbenzene (see Table 6)... Fig. 9. Scanning electron micrographs of surface and cross-sections of beaded resins obtained by suspension copolymerization of AOTcp with styrene and divinylbenzene (see Table 6)...
Scanning electron micrographs of surface defects on (a) The inner surface of a blow-moulded HOPE bottle (b) a polyethylene injection moulding. In both micrographs the ridges run at 90° to the flow direction. [Pg.191]

Fig. 20.8 Scanning electron micrographs of surface of single-layer Celgard separators used in lithium batteries (a) 2400 (PP) small pore, (b) 2500 (PP) large pore, and (c) 2730 (PE). Reprinted with permission from Chem. Rev. 104 (2004) 4419-4462, copyright (2004), American Chemical Society... Fig. 20.8 Scanning electron micrographs of surface of single-layer Celgard separators used in lithium batteries (a) 2400 (PP) small pore, (b) 2500 (PP) large pore, and (c) 2730 (PE). Reprinted with permission from Chem. Rev. 104 (2004) 4419-4462, copyright (2004), American Chemical Society...
Fig. 4.6.6 Scanning electron micrographs of surfaces of HiPco coatings dispersed in THF with (a) the aid of a VA/AA copolymer dispersing agent at 1 1 VA/AA-to-HiPco wt/wt ratio and (b) without the aid of a polymer dispersing agent/binder. The better definition of the rope stmcrnre in (a) indicates a higher electrical conductivity on the nanombe surface (With permission firom Caneba and Axland, 2004)... Fig. 4.6.6 Scanning electron micrographs of surfaces of HiPco coatings dispersed in THF with (a) the aid of a VA/AA copolymer dispersing agent at 1 1 VA/AA-to-HiPco wt/wt ratio and (b) without the aid of a polymer dispersing agent/binder. The better definition of the rope stmcrnre in (a) indicates a higher electrical conductivity on the nanombe surface (With permission firom Caneba and Axland, 2004)...
Figure 3.9 Scanning electron micrograph of surface morphology of hydrogels prepared with pachyman (A), CMP (B) and HMP (C) crosslinked with epichlorohydrin (A and C reproduced with permission from [77] and B reproduced with permission from [213]). Figure 3.9 Scanning electron micrograph of surface morphology of hydrogels prepared with pachyman (A), CMP (B) and HMP (C) crosslinked with epichlorohydrin (A and C reproduced with permission from [77] and B reproduced with permission from [213]).
Figure 5.24. Scanning electron micrograph of surface of Lima graphite after oxidation in air to... Figure 5.24. Scanning electron micrograph of surface of Lima graphite after oxidation in air to...
The changes in topographical features, induced by catalytic gasification, are quite different from those changes induced in pure carbons. These changes are best described by examination of scanning electron micrographs of surfaces of oxidized carbons. [Pg.273]

Figures 5.28. Scanning electron micrograph of surface of a non-graphitizable carbon from PFA, HTT 1123 K, with a nickel content of Ni C of 1 4500, oxidized in carbon dioxide at 873 K to 18 wt% bum-off. Figures 5.28. Scanning electron micrograph of surface of a non-graphitizable carbon from PFA, HTT 1123 K, with a nickel content of Ni C of 1 4500, oxidized in carbon dioxide at 873 K to 18 wt% bum-off.

See other pages where Scanning electron micrograph of surface is mentioned: [Pg.1533]    [Pg.200]    [Pg.100]    [Pg.6]    [Pg.117]    [Pg.701]   


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Electron micrograph

Electron micrographs

Electron micrographs, scanning

Scanning electron micrograph

Scanning electron micrographic

Surface electronic

Surface electrons

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