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Dissolved Fe(II) concentrations were quantified after sample centrifugation at 15,000 × g for 10 min and subsequent filtration through 0.2 μm filters (Spartan 13/0.2 RC; Whatman).
With this IBL, the IMCs of Ag2In and Ag9In4 with high temperature resist to post-bonding process are derived under process condition of wafer bonding at 180 °C, 40 min and subsequent 120 130 °C annealing for 24 h.
The volatile compounds showed optimal extraction using a DVB/CAR/PDMS fiber, incubation of 5 ml of wine with 2 g NaCl at 45 °C during 5 min, and subsequent extraction of 30 min at the same temperature.
In order to have fast and complete recovery, a heating procedure for a fixed duration (10 min) and subsequent cooling to room temperature was followed in a step sequence controlled by a temperature controller.
CNT specimens were obtained by pressing and sintering of a mixture of the components in the argon atmosphere at the temperature Т = 380°C ± 5°C during 10 min and subsequent rolling of the produced piece.
As a result, the reversible hydrogen absorption capability was in excess of 90% of the theoretical value of 6.8 wt.% under the absorption parameters of 350 °C and 1 MPa for 24 min and subsequent desorption at 0.2 MPa for 24 min after activation.
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The etched height of the WL is about 0.7, 1.0, and 0.4 nm for the first 2-min and subsequent 5- and 10-min NHH etching, respectively, giving the Ge content of about 45%% for original WL surface and about 40 and 30%% for 2- and 7-min NHH-etched WL surface, respectively.
A thermal cycle consisting of a 54 min run and subsequent a 6 min pause was repeated four times, and a processed specimen was analyzed in terms of the deposition and oxidation of the substrate.
Following 0.5-min vortex and subsequent 10-min centrifugation, the organic phase was transferred to a 2-ml vial and evaporated to dryness under vacuum at 43°C.
Plasma proteins were removed by precipitation with acetonitrile (10 min, 4°C) and subsequent centrifugation and ultrafiltration.
Clostridium counts were obtained after pretreatment of the faecal sample in 80% ethanol for 15 min. and subsequent culture on Columbia blood agar after 4 days of anaerobic incubation at 37°C.
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