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I.v. Controllers

Medications under the control of the US Drug Enforcement Agency (Schedules I-V controlled substances) are indicated by the symbol (C). Most medications are uncontrolled" and do not require a DEA prescriber number on the prescription. The following is a general description for the schedules of DEA-controlled substances ... [Pg.441]

The first controller GCuS) sees a coupled openloop transfer function in which the second controller is nested, because the controller Gq ,> is on automatic. The 67 i(v) controller is tuned by finding the ultimate gain and period and using the Tyreus-Luyben settings. The settings of this PI controller are Kc2 = 2.13 and r/2 = 1.94. [Pg.375]

A checklist analysis (CCPS, 1992) verifies the status of a system. It is versatile, easy and applicable at any life-cycle stage of a process. It is primarily used to show compliance with standards and practices by cost-effectively identifying hazards, chlorine Tar> <- liccklists provide commonality for management K.-, icw of hazard assessments. It may be used for controlling a proces.s from development to decommissioning. Approvals by appropriate authorities Cl i( V each stage of a project. [Pg.77]

C.G. Vayenas, I.V. Yentekakis, S.I. Bebelis, and S.G. Neophytides, In situ Controlled Promotion of Catalyst Surfaces via Solid Electrolytes The NEMCA effect, Ber. Buns. Phys. Chem. 99(11), 1393-1401 (1995). [Pg.14]

I.V. Yentekakis, R.M. Lambert, M.S. Tikhov, M. Konsolakis, and V. Kiousis, Promotion by sodium in emission control catalysis A kinetic and spectroscopic study of the Pd-catalyzed reduction on NO by propene, J. Catal. 176, 82-92 (1998). [Pg.328]

I.V. Yentekakis, and C.G. Vayenas, In situ controlled promotion of Pt for CO oxidation via NEMCA using CaF2 as the solid electrolyte, J. Catal. 149, 238-242(1994). [Pg.433]

I.V. Yentekakis, C.A. Pliangos, V.G. Papadakis, X.E. Verykios, and C.G. Vayenas, Support and NEMCA-induced Promotional Effects on the Activity of Automotive Exhaust Catalysts in A. Frennet and Journal-M. Bastin (eds.) Catalysis and Automotive Pollution Control HI, Stud. Surf. Sci. Catal. 96, 375-385 (1995). [Pg.512]

Poly(DL-lactide) was used as the excipient in microspheres of CCNU, a nitrosourea, prepared by a solvent evaporation procedure (96,97). PLA-CCNU microspheres 3.0 pm in diameter were injected i.v. and leukemia cell survival was determined by spleen colony assay. A 100-fold decrease in leukemia cell survival was observed with the microspheres in both spleen and liver compared to untreated controls. Promising results were also obtained with Lewis lung carcinoma in mice. These studies showed that 2- to 4-ym microspheres were preferentially targeted to the lungs. [Pg.21]

Figure 7.4 Dose-response effects of MDMA on extracellular levels of endogenous 5-HT (left panel) and DA (right panel) in rat nucleus accumbens. Male rats undergoing in vivo microdialysis received i.v. injections of 1 and 3 mg/kg MDMA at 0 and 60 min, respectively. Dialysate levels of 5-HT and DA were assayed by HPLC-ECD. Data are mean SEM, expressed as pg/5 pi sample, for N = 6 rats/group. Baseline levels of 5-HT and DA were 0.22 0.03 and 1.44 0.24 pg/5 pi, respectively. Significant with respect to pre-injection control (P < 0.05 Duncan s). See Baumann et al.39 for methods. Figure 7.4 Dose-response effects of MDMA on extracellular levels of endogenous 5-HT (left panel) and DA (right panel) in rat nucleus accumbens. Male rats undergoing in vivo microdialysis received i.v. injections of 1 and 3 mg/kg MDMA at 0 and 60 min, respectively. Dialysate levels of 5-HT and DA were assayed by HPLC-ECD. Data are mean SEM, expressed as pg/5 pi sample, for N = 6 rats/group. Baseline levels of 5-HT and DA were 0.22 0.03 and 1.44 0.24 pg/5 pi, respectively. Significant with respect to pre-injection control (P < 0.05 Duncan s). See Baumann et al.39 for methods.
Figure 7.9 Effects of MDMA pretreatment on secretion of corticosterone (left panel) and prolactin (right panel) evoked by acute MDMA challenge. Male rats received three i.p. injections of 1.5 or 7.5 mg/kg MDMA, one dose every 2 h. Saline was administered on the same schedule. Then 2 weeks later rats received i.v. injections of 1 and 3 mg/kg MDMA. Blood samples were drawn via indwelling catheters plasma corticosterone and prolactin were measured by RIA.126 Data are mean SEM, expressed as ng/ml of plasma for N = 8 rats/group. Baseline corticosterone and prolactin levels were 73 18 and 2.4 0.6 ng/ml of plasma, respectively. Significant compared to saline-pretreated control group (P < 0.05 Duncan s). Figure 7.9 Effects of MDMA pretreatment on secretion of corticosterone (left panel) and prolactin (right panel) evoked by acute MDMA challenge. Male rats received three i.p. injections of 1.5 or 7.5 mg/kg MDMA, one dose every 2 h. Saline was administered on the same schedule. Then 2 weeks later rats received i.v. injections of 1 and 3 mg/kg MDMA. Blood samples were drawn via indwelling catheters plasma corticosterone and prolactin were measured by RIA.126 Data are mean SEM, expressed as ng/ml of plasma for N = 8 rats/group. Baseline corticosterone and prolactin levels were 73 18 and 2.4 0.6 ng/ml of plasma, respectively. Significant compared to saline-pretreated control group (P < 0.05 Duncan s).
Yang, I. V. (2006). Use of external controls in microarray experiments. Methods Enzymol. 411, 50-63. [Pg.234]

Electrolyzers are generally current-controlled, which means that a certain DC is imposed according to the desired hydrogen production. In a wind-hydrogen system, the wind turbine power available for the operation of the electrolyzer is generally known therefore, the power input should be transformed to a current input. The voltage-current relation of an electrolyzer is not very simple because it depends on the temperature, pressure, and other construction characteristics. For a given electrolyzer, it is possible to experimentally establish the I-V curve at different temperatures and pressures, and deduce a temperature-dependent current-power curve. [Pg.173]

Successive extractions, whilst increasing the efficiency of extraction of both solutes, may lead to a poorer separation. For example, if DA = 102 and I)v = 10 one extraction will remove 99.0% of A and 9.1% of B whereas two extractions will remove 99.99% of A but 17% of B. In practice, a compromise must frequently be sought between completeness of extraction and efficiency of separation. It is often possible to enhance or suppress the extraction of a particular solute by adjustment of pH or by complexation. This introduces the added complication of several interrelated chemical equilibria which makes a complete theoretical treatment more difficult. Complexation and pH control are discussed more fully in Chapter 3. [Pg.53]


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See also in sourсe #XX -- [ Pg.244 ]




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