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Scanning electron micrographs of positive

Figure 10. Scanning electron micrographs of positive (top, 3.5 mJ/cm2) and negative images (bottom, 3.0 mJ/cm2) heated at 200°C for 30 min (the positive image was re-exposed to 2.8 mJ/cm2 of 254 nm radiation and baked at 130 C for 2 min prior to the 200°C bake). Figure 10. Scanning electron micrographs of positive (top, 3.5 mJ/cm2) and negative images (bottom, 3.0 mJ/cm2) heated at 200°C for 30 min (the positive image was re-exposed to 2.8 mJ/cm2 of 254 nm radiation and baked at 130 C for 2 min prior to the 200°C bake).
Fig. 13 Scanning electron micrographs of positive (top) and negative (bottom) images delineated in fBOC resist by X-ray irradiation [15,16]... Fig. 13 Scanning electron micrographs of positive (top) and negative (bottom) images delineated in fBOC resist by X-ray irradiation [15,16]...
Figure 4. Scanning Electron Micrograph of Positive Image of the Acetal-protected Poly(vinylphenol) 15 mJ/cm of 254 nm Radiation and Baked at 95 C for 2 Minutes. Figure 4. Scanning Electron Micrograph of Positive Image of the Acetal-protected Poly(vinylphenol) 15 mJ/cm of 254 nm Radiation and Baked at 95 C for 2 Minutes.
Figure IS. Scanning electron micrograph of positive images in pofymer 3d containing 10 wt% of triphenylsulfonium triflate, exposed to 100 ju,C/cm of electron beam(20kV), postbaked at 100 °C for 10 min, and then developed with TMAHaq(0.1%) for 15 sec. Line space 0.5 /u.m. Figure IS. Scanning electron micrograph of positive images in pofymer 3d containing 10 wt% of triphenylsulfonium triflate, exposed to 100 ju,C/cm of electron beam(20kV), postbaked at 100 °C for 10 min, and then developed with TMAHaq(0.1%) for 15 sec. Line space 0.5 /u.m.
Fig. 2.19 Scanning electron micrographs of Tego Magnan powder (a) milled for 100 h under the high-energy impact mode (IMP68 with two magnets at six and eight o clock positions) and (b) after three cycles of desorption at 350°C under 0.1 MPaH pressure for 15 min/annealing at 350°C under pre-vacuum for 15 min/absorption at 350°C under 3.2 MPa pressure for 15 min... Fig. 2.19 Scanning electron micrographs of Tego Magnan powder (a) milled for 100 h under the high-energy impact mode (IMP68 with two magnets at six and eight o clock positions) and (b) after three cycles of desorption at 350°C under 0.1 MPaH pressure for 15 min/annealing at 350°C under pre-vacuum for 15 min/absorption at 350°C under 3.2 MPa pressure for 15 min...
Fig. 1.5.8 Scanning electron micrograph of poly(p-fer-butylstytene) particles obtained by polymerization of monomer droplets in the aerosol phase. The monomer and initiator flow rates were 1.2 dm3 min-1 and 40 cm5 min-1 and the boiler and initiator reservoir temperatures were 50°C and 25°C, respectively. The initiator was injected into the flowing aerosol at two positions. The modal diameter of these particles is 1.8 [xm. (From Ref. 67.)... Fig. 1.5.8 Scanning electron micrograph of poly(p-fer-butylstytene) particles obtained by polymerization of monomer droplets in the aerosol phase. The monomer and initiator flow rates were 1.2 dm3 min-1 and 40 cm5 min-1 and the boiler and initiator reservoir temperatures were 50°C and 25°C, respectively. The initiator was injected into the flowing aerosol at two positions. The modal diameter of these particles is 1.8 [xm. (From Ref. 67.)...
Figure 11. (A) Scheme of the PDMS microfluidic device. Inset channel crossing with the cell trap composed of microstmctured obstacles, (B) Scanning electron micrograph of the cell trap, (C) single cell in a channel navigated by optical tweezers in the microchannel, (D-G) optical micrographs of a single cell at the injection position during SDS lysis. SDS flow is from channel 4 through the cell trap into channel 2. Figure 11. (A) Scheme of the PDMS microfluidic device. Inset channel crossing with the cell trap composed of microstmctured obstacles, (B) Scanning electron micrograph of the cell trap, (C) single cell in a channel navigated by optical tweezers in the microchannel, (D-G) optical micrographs of a single cell at the injection position during SDS lysis. SDS flow is from channel 4 through the cell trap into channel 2.
Scanning electron micrographs of a separator from a wet-charged battery after 9 months of storage. Separator surface facing (a) positive plate (b) negative plate. [Pg.565]

Fig. 6 Scanning electron micrographs of the inside of a carbon coated (left) and an uncoated (right) PTFE vascular prosthesis (central sections both) after 4 weeks in carotis position of beagles. Both prostheses were patent on explantation... Fig. 6 Scanning electron micrographs of the inside of a carbon coated (left) and an uncoated (right) PTFE vascular prosthesis (central sections both) after 4 weeks in carotis position of beagles. Both prostheses were patent on explantation...

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Electron micrograph

Electron micrographs

Electron micrographs, scanning

Position scanning

Positional scan

Positional scanning

Scanning electron micrograph

Scanning electron micrographic

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