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Wafer extract

Figure 10.133 Trace analysis of anions in a wafer extract. Separator column lonPac ASM column dimensions 250mm X2 mm i.d. eluent 6.75mmol/L NaOH + 9mmol/L H3BO3 after 3.5 min to 30mmol/L NaOH+40mmol/L H3BO3 flow rate 0.75 mL/min detection ... Figure 10.133 Trace analysis of anions in a wafer extract. Separator column lonPac ASM column dimensions 250mm X2 mm i.d. eluent 6.75mmol/L NaOH + 9mmol/L H3BO3 after 3.5 min to 30mmol/L NaOH+40mmol/L H3BO3 flow rate 0.75 mL/min detection ...
Fig. 9-73. Trace analysis of anions in a wafer extract. - Separator column lonPac AS14 (2-mm) eluant 6.75 mmol/L NaOH + 9 mmol/L H3BO3 after 3.5 min to 30 mmol/L NaOH + 40 mmol/L H3BO3 flow rate 0.75 mL/min detection suppressed conductivity injection volume 1 mL solute concentrations 1.5 pg/L each of fluoride (1). acetate (2), and formate (3), 11 pg/L chloride (4), unknown component (5), carbonate (6), 2.3 pg/L nitrate (7), and 10pg/L sulfate (8). Fig. 9-73. Trace analysis of anions in a wafer extract. - Separator column lonPac AS14 (2-mm) eluant 6.75 mmol/L NaOH + 9 mmol/L H3BO3 after 3.5 min to 30 mmol/L NaOH + 40 mmol/L H3BO3 flow rate 0.75 mL/min detection suppressed conductivity injection volume 1 mL solute concentrations 1.5 pg/L each of fluoride (1). acetate (2), and formate (3), 11 pg/L chloride (4), unknown component (5), carbonate (6), 2.3 pg/L nitrate (7), and 10pg/L sulfate (8).
Fig. 12.6 Small-grain crack-free Gao.8lno.2Sb wafer extracted from a polyc stal grown using vertical Bridgman technique with an oscillating baffle near the melt/solid interface. Fig. 12.6 Small-grain crack-free Gao.8lno.2Sb wafer extracted from a polyc stal grown using vertical Bridgman technique with an oscillating baffle near the melt/solid interface.
Fig. 12.8 Large-grain crack-free G30.25 no.75 Sb wafer extracted from a polycrystal grown using VGF with ACRT. Fig. 12.8 Large-grain crack-free G30.25 no.75 Sb wafer extracted from a polycrystal grown using VGF with ACRT.
A typical LIMS instrument accepts specimens up to 19 mm (0.75 in) in diameter and up to 6 mm in thickness. Custom designed instruments exist, with sample manipulation systems that accept much larger samples, up to a 6-in wafer. Although a flat sample is preferable and is easier to observe with the instrument s optical system, irregular samples are often analyzed. This is possible because ions are produced and extracted from pm-sized regions of the sample, without much influence from nearby topography. However, excessive sample relief is likely to result in reduced ion signal intensity. [Pg.596]

Rejeb et al. described the development and characterization of immunoafflnity columns for the selective extraction of thifluzamide in peanuts. Efficient recovery was achieved using a simple elution profile requiring only 4 mL of methanol-wafer. De Jager and Andrews " described a novel fasf screening method for organochlorine... [Pg.733]

Solvent extracts" Cast directly on the KBr and evaporate solvent Cast on to silicon wafer Large areas can be coated, no moisture absorption and no interfering peaks... [Pg.314]

Depending on the colour and use of the finished wafer some wafers are made from brown flours. While the increased fibre content has nutritional advantages the real reason for this is that the higher extraction rate makes the flour cheaper to produce. [Pg.224]

The calibration was done for temperatures between 25 °C and 325 °C. The data were fitted according to Eq. (4.1), and the two temperature coefficients were extracted. Within the same wafer batch, a production-spread-induced error of 2% in the determination of the microhotplate temperature coefficients was observed. [Pg.37]

These equations describe an unheated transistor and were verified for a device with no backside etching (no membrane). The modelling parameters were provided by the manufacturer, whereas the value of the threshold voltage was taken from wafer map data. The channel length modulation parameter. A, had to be extracted from measurement data. The discrepancy between simulated and measured source-drain saturation current, fsd,sat> for a transistor embedded in the bulk silicon was less than 1%, which confirmed the vaHdity of the model assumptions. [Pg.53]

Laxative effect. Seed hull, taken orally by adults at a dose of 7 g/person, increased weekly fecal mass without influencing transit time or frequency . Seedcoat, administered orally to 80 patients at a dose of 6.4 g/person three times daily, was active in a blinded placebo controlled study of efficacy of extract in treatment of irritable bowel syndrome " . Water extract of the dried kernel, administered orally to 40-year-old adults of both sexes, was active . Seed powder, administered orally to adults of both sexes, was active. Biological activity reported has been patented ". Dried seeds, administered orally to adults at a dose of 0.5 g/person, were active. Placing the seeds in water increased their volume, 90% alcohol produced a decrease in volume to normal seed size, and linseed oil had no effect on volume. The seed mucilage remained in gel form and is considered preferable to the solid form because it is more easily digested " . Dried seed powder, administered orally to 35 patients with chronic constipation at a dose of 50 mg/person, was active in a controlled, double-blind study " . Fiber, administered orally to adults, was active. Psyllium fiber and sennosides were prepared into a wafer to be... [Pg.429]

Transport properties play an important role in chemical reactions, electrochemistry, and liquid-liquid extraction. This concerns mainly the viscosity of ILs and fheir solutions wifh molecular solvenfs. Viscosity of ILs, typically at the level of 10-500 cP af room femperafure, is much higher than that characteristic of wafer ( /(HjO) = 0.89 cP af 298.15 K) and aqueous solutions. The high dynamic viscosity (viscosity coefficient) of ILs causes difficulties... [Pg.6]

Additionally, ILs may serve as a convenient medium for analysis affer exfracfion. For example, fheir ionic nature opens an exciting opportunity of direcf elecfrochemical analysis of the extract, impossible for mosf of fhe conventional wafer-immiscible solvents. [Pg.244]

The extraction of pentachlorophenol (PCP) from pressure-treated wood wafers with supercritical carbon dioxide (SC-CO2) was studied in a continu-ons-flow extractor (Sahledemessie et al., 1997). [Pg.149]

Differenf sampling mefhods often result in collection of differenf com-ponenfs of the element or compound of interest. Most seawater samples are collected in bottles, filtered to remove particles and analyzed directly or after preconcentration of minor components. Particulate matter from fhe wafer column is collecfed by filtration or with sediment traps. Sediment samples are collected in cores that recover intact chronological sequences and are commonly subsampled, dried and groxmd to a powder. Pore waters are extracted from sedimenfs by squeezing or suction, dialysis, and centrifugation. [Pg.21]

Tsai, C.Y., Chen, Y.F., Chen, W.C., Yang, F.R., Chen, J.H. and Lin, J.C. (2005) Separation of gallium and arsenic in wafer grinding extraction solution using a supported liquid membrane that contains PC88A as a carrier. Journal of Environmental Science and Health Part A-Toxic/Hazardous Substances e[ Environmental Engineering, 40, 477. [Pg.542]

In the experiments of O Connor et al. [10,47,48], monodisperse fractions of Z and Zdol, which were fractionated via supercritical fluid extraction in CO2, were dip-coated onto the surface of silicon wafers. Film thickness was controlled... [Pg.7]

Polycrystalline silicon, produced from silane (SiH4) or trichlorosilane (SiHCl3) forms the upstream part of the semiconductor sector. Monocrystalline silicon is extracted from polycrystalline silicon and sliced into wafers 25 microns thick and 8 to 10 centimeters in diameter. [Pg.36]

In the simplest measurement, data collected for two energies can provide a measure of the escape depth, the porosity and the open porosity fraction. The values are extracted by comparing the measurements to a set of calibration curves. With a positron beam flux of 0.2 pA, 100 locations on a wafer could be checked in 30 minutes. Mean lifetime measurements can be carried out with a pulsed positron beam. An intermediate time resolution of about 1 ns will be sufficient. A single measurement can be accomplished in about 1 minute. [Pg.205]

To a solution of 4.0 g. (0.012 mole) of iridium tetrachloride (Note 1) in 4.5 ml. of concentrated hydrochloric acid is added ISO ml. of water followed by 50 ml. of trimethyl phosphite (Note 2). This solution is added to a solution of 30.8 g. (0.20 mole) of 4-t-butylcyclohexanone (Note 3) in 635 ml. of 2-propanol contained in a 2-1. flask equipped with a reflux condenser. The solution is heated at reflux for 48 hours (Note 4). At the end of this time the 2-propanol is removed on a rotary evaporator at reduced pressure, and the remaining solution is diluted with 250 ml. of water and extracted with four 150-ml. portions of el her. The ether solution is washed with two 100-ml. portions of wafer which are combined with the aqueous residue (Note 5). Tin ether extract is dried over magnesium sulfate or potassium carbonate and then concentrated on a rotary evaporator at reduced pressure to obtain cis-4-t-butylcyclohexano] as a w hite solid (2ft—31 g. 93-99%). Analysis of the crude product by glpc demonstrates it to contain 95.8-96.2 % eis-alcohol and 12 3 8 % of the trans isomer with essentially no ketone remaining (Note 6). Itecrystallization from 40% aqueous ethanol an nrds greater than 99% pure ri.s-alcohol, m.p. 82-83.5° after Hiihlimulion2 (Nole 7). [Pg.13]

The amplitude of the oscillations in reflected light intensity appears to remain constant as the blends dissolve. This would indicate that the undissolved portion of the film is not undergoing swelling or extraction to any noticeable extent. The second feature, observable especially in the high molecular weight PMMA blend, is an increased offset between the maximum amplitude during dissolution and the reflection from the bare wafer after dissolution is complete (Figure 6). [Pg.155]

Phenol (3).2 Anisole 1 (107 g, 1 mol) and pyndine HCI2 (130 g, 1.3 mol) were heated with AcOH (5-10 mL) for 5 h af 190 C The mixture was poured info wafer (500 mL) and extracted with EtzO. Prom the EtgO solutions 3 was extracted with NaOH and the alkaline solution was saturated wKh COg. Extraction with ether and distllation of the extract afforded 94 g of 3 (100%),mp35-40 C... [Pg.450]


See other pages where Wafer extract is mentioned: [Pg.1124]    [Pg.656]    [Pg.1124]    [Pg.656]    [Pg.119]    [Pg.119]    [Pg.395]    [Pg.32]    [Pg.696]    [Pg.68]    [Pg.216]    [Pg.146]    [Pg.49]    [Pg.69]    [Pg.44]    [Pg.24]    [Pg.91]    [Pg.376]    [Pg.122]    [Pg.144]    [Pg.395]    [Pg.423]    [Pg.91]    [Pg.336]    [Pg.194]    [Pg.153]    [Pg.193]    [Pg.195]    [Pg.421]    [Pg.447]   
See also in sourсe #XX -- [ Pg.3 , Pg.1124 ]




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