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Specifications for hGH products are defined by the governmental licensing authorities, eg, the U.S. Pood and Dmg Administration. Draft monographs for hGH have been prepared by both the EnitedStates Pharmacopia and the European Pharmacopeia commissions and should be formally adopted by 1995. These specifications are suitable for biosynthetic hGH. The much less purified pituitary-derived hGH has virtually disappeared from commercial production. An international reference standard for pituitary-derived hGH (lot 80/505) has been used for caUbration, particularly for bioassay purposes. A highly purified biosynthetic hGH standard (lot 88/624) has been prepared and should be formally adopted by 1995, or before. [Pg.197]

Inductively coupled argon plasma (icp) and direct current argon plasma (dcp) atomic emission spectrometry are solution techniques that have been appHed to copper-beryUium, nickel—beryUium, and aluminum—beryUium aUoys, beryUium compounds, and process solutions. The internal reference method, essential in spark source emission spectrometry, is also useful in minimizing drift in plasma emission spectrometry (17). Electrothermal (graphite... [Pg.68]

The reaction of bis(benzene)vanadium [12129-72-5] with TCNE affords an insoluble amorphous black soHd that exhibits field-dependent magnetization and hysteresis at room temperature, an organic-based magnet (12). The anion radical is quite stable in the soHd state. It is paramagnetic, and its intense electron paramagnetic resonance (epr) spectmm has nine principal lines with the intensity ratios expected for four equivalent N nuclei (13) and may be used as an internal reference in epr work (see Magnetic spin resonance). [Pg.403]

The analysis was performed by XRF method with SR. SRXRF is an instrumental, multielemental, non-destructive analytical method using synchrotron radiation as primary excitation source. The fluorescence radiation was measured on the XRF beam-line of VEPP-3 (E=2 GeV, 1=100 mA), Institute of Nuclear Physics, Novosibirsk, Russia. For quality control were used international reference standards. [Pg.430]

The internal reference presented to the voltage error amplifier is 2.5 V +1-2.5 percent. [Pg.166]

Most instruments of this type incorporate built-in selfchecking facilities but the check can only be as accurate as the internal reference which, itself, will only be accurate over a specific range. The instrument should be calibrated against a reference source at periodic intervals. [Pg.240]

The preparation of an international reference book such as this could not possibly be achieved without the total cooperation of so many individual authors and the backing of their various employers, especially where company contributions have been made, bringing together a wealth of professional knowledge and expertise. [Pg.1118]

The pressed disc (or pellet) type of crystalline membrane electrode is illustrated by silver sulphide, in which substance silver ions can migrate. The pellet is sealed into the base of a plastic container as in the case of the lanthanum fluoride electrode, and contact is made by means of a silver wire with its lower end embedded in the pellet this wire establishes equilibrium with silver ions in the pellet and thus functions as an internal reference electrode. Placed in a solution containing silver ions the electrode acquires a potential which is dictated by the activity of the silver ions in the test solution. Placed in a solution containing sulphide ions, the electrode acquires a potential which is governed by the silver ion activity in the solution, and this is itself dictated by the activity of the sulphide ions in the test solution and the solubility product of silver sulphide — i.e. it is an electrode of the second kind (Section 15.1). [Pg.560]

Because an increase in resolution causes a decrease in sensitivity, it is best to operate at the lowest resolution commensurate with good results. Some instrument data systems will allow calibration with an external reference material such as perfluorokerosene and then use of a secondary reference material for the internal mass reference. Tetraiodothiophene, vaporized using the solids probe inlet, is recommended as the secondary reference. The accurate masses are 79.9721, 127.9045, 162.9045, 206.8765, 253.8090, 293.7950, 333.7810, 460.6855, and 587.5900. For a higher mass standard, use hexaiodobenzene. Because the mass defect for these internal reference ions are so large, a resolution of 2000 is ample to separate these ions from almost any sample ions encountered in GC/MS. [Pg.375]

The spectral properties of pentafluorophenylcopper te-tramer are as follows infrared (Nujol) cm. 1630 medium 1391 medium 1353 medium 1275 medium 1090,1081, and 1071 strong triplet 978 strong 785 medium fluorine magnetic resonance (tetrahydrofuran with trichlorofluoromethane as internal reference) 8 (multiplicity, number of fluorines, assignment, coupling constant J in Hz.) 107.2 (20-line multiple , 2, ortho F), 153.4 (triplet of triplets, 1, para F, J= 1.3 and 20), 162.3 (17-line multiplet, 2, meta F). Absorptions at 820-900, 1100-1125, and 1290 cm.- in the infrared spectrum and at 8 3.05 in the proton magnetic resonance spectrum indicate that dioxane is still present. [Pg.64]

TEM observation and elemental analysis of the catalysts were performed by means of a transmission electron microscope (JEOL, JEM-201 OF) with energy dispersion spectrometer (EDS). The surface property of catalysts was analyzed by an X-ray photoelectron spectrometer (JEOL, JPS-90SX) using an A1 Ka radiation (1486.6 eV, 120 W). Carbon Is peak at binding energy of 284.6 eV due to adventitious carbon was used as an internal reference. Temperature programmed oxidation (TPO) with 5 vol.% 02/He was also performed on the catalyst after reaction, and the consumption of O2 was detected by thermal conductivity detector. The temperature was ramped at 10 K min to 1273 K. [Pg.518]

Pybus, J. Feldman, F. J. and Bowers, 6. N., Jr. Measurement of total calcium in serum by atomic absorption spectrophotmetry with use of a strontiim internal reference. Clin. Chem. (1970), lj6, 998 - 1007. [Pg.151]

INHRR laboratories are Centres for International Reference on Biological Products, diagnosis kits for Andean area, and are part of the network of quality labs for Pan- American Sanitary Office (OPS) coordinated by the USP. They also participate in OMCL survey. [Pg.104]

A representative ISE is shown schematically in Fig. 1. The electrode consists of a membrane, an internal reference electrolyte of fixed activity, (ai)i , ai and an internal reference electrode. The ISE is immersed in sample solution that contains analyte of some activity, (ajXampie and into which an external reference electrode is also immersed. The potential measured by the pH/mV meter (Eoe,) is equal to the difference in potential between the internal (Eraf.int) and external (Eref.ext) reference electrodes, plus the membrane potential (E emb), plus the liquid junction potential... [Pg.4]

One barrel-tip contains the organic membrane phase and an internal reference electrode the other constitutes a second reference electrode. A four-barrel configuration with a 1-pm tip in which three barrels are liquid membrane electrodes for Na, Ca and and the fourth is a reference electrode has been reported Some representative applications of ion-selective electrodes for intracellular measurements are shown in Table 3. [Pg.14]

Chemical and pharmaceutical manufacturers must establish their own internal reference materials, when no pharmacopoeial monograph exists, to satisfy the requirements of Good Manufacturing Practice (European Commission 1997). [Pg.173]

Fig. 3.16 Schematic drawing of the MIMOS II Mossbauer spectrometer. The position of the loudspeaker type velocity transducer to which both the reference and main Co/Rh sources are attached is shown. The room temperature transmission spectrum for a prototype internal reference standard shows the peaks corresponding to hematite (a-Fe203), a-Fe, and magnetite (Fe304). The internal reference standards for MIMOS II flight units are hematite, magnetite, and metallic iron. The backscatter spectrum for magnetite (from the external CCT (Compositional Calibration Target) on the rover) is also shown... Fig. 3.16 Schematic drawing of the MIMOS II Mossbauer spectrometer. The position of the loudspeaker type velocity transducer to which both the reference and main Co/Rh sources are attached is shown. The room temperature transmission spectrum for a prototype internal reference standard shows the peaks corresponding to hematite (a-Fe203), a-Fe, and magnetite (Fe304). The internal reference standards for MIMOS II flight units are hematite, magnetite, and metallic iron. The backscatter spectrum for magnetite (from the external CCT (Compositional Calibration Target) on the rover) is also shown...
Fig. 3.19 Schematic illustration of the measurement geometry for Mossbauer spectrometers. In transmission geometry, the absorber (sample) is between the nuclear source of 14.4 keV y-rays (normally Co/Rh) and the detector. The peaks are negative features and the absorber should be thin with respect to absorption of the y-rays to minimize nonlinear effects. In emission (backscatter) Mossbauer spectroscopy, the radiation source and detector are on the same side of the sample. The peaks are positive features, corresponding to recoilless emission of 14.4 keV y-rays and conversion X-rays and electrons. For both measurement geometries Mossbauer spectra are counts per channel as a function of the Doppler velocity (normally in units of mm s relative to the mid-point of the spectrum of a-Fe in the case of Fe Mossbauer spectroscopy). MIMOS II operates in backscattering geometry circle), but the internal reference channel works in transmission mode... Fig. 3.19 Schematic illustration of the measurement geometry for Mossbauer spectrometers. In transmission geometry, the absorber (sample) is between the nuclear source of 14.4 keV y-rays (normally Co/Rh) and the detector. The peaks are negative features and the absorber should be thin with respect to absorption of the y-rays to minimize nonlinear effects. In emission (backscatter) Mossbauer spectroscopy, the radiation source and detector are on the same side of the sample. The peaks are positive features, corresponding to recoilless emission of 14.4 keV y-rays and conversion X-rays and electrons. For both measurement geometries Mossbauer spectra are counts per channel as a function of the Doppler velocity (normally in units of mm s relative to the mid-point of the spectrum of a-Fe in the case of Fe Mossbauer spectroscopy). MIMOS II operates in backscattering geometry circle), but the internal reference channel works in transmission mode...
MIMOS II has three temperature sensors one on the electronics board and two on the SH. One temperature sensor in the SH is mounted near the internal reference absorber, and the measured temperature is associated with the reference absorber and the internal volume of the SH. The other sensor is mounted outside the SH at the contact ring assembly. It gives the approximate analysis temperature for the sample on the Martian surface. This temperature is used to route the Mossbauer data to the different temperature intervals (maximum of 13, with the temperature width software selectable) assigned in memory areas. Shown in Fig. 3.21 are the data of the three temperature sensors taken on Mars (rover Opportunity at Meridiani Planum) in January 2004 between 12 10 PM on Sol 10 (10 Martian days after landing) and 11 30 AM on Sol 11. The temperature of the electronics board inside the rover is much higher than the temperatures inside the SH and the contact plate sensor, which are nearly identical and at ambient Martian temperature. [Pg.62]

The primary method for velocity cahbration is the internal reference channel with reference target and detector configured in transmission geometry (Fig. 3.16). [Pg.66]

MIMOS II has three temperature sensors, one on the electronics board and two on the sensor head. One temperature sensor in the sensor head is mounted near the internal reference absorber, and the measured temperature is associated with the reference absorber and the internal volume of the sensor head. The other sensor is mounted outside the sensor head at the contact ring assembly. It gives the analysis temperature for the sample on the Martian surface. This temperature is used to route... [Pg.449]

Ref 63. The value is revised by employing Mc4N as an internal reference in the place of -Bu4N. ... [Pg.59]

Experimentally, Ao j/2 is generally considered equal to the midpeak potential, and is then directly deduced from the voltammograms. This does not generate experimental errors, since an ion of known standard transfer potential (for instance, tetramethyl ammonium, TMA+) must be used as an internal reference to transpose the experimental potential scale (noted E) to the absolute Galvani potential scale, so that is obtained by ... [Pg.742]


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Absolute internal reference

An Internal Realist Account of Reference

Chemical shift internal reference

Chiral X-ray internal reference

Internal Reference Standards immunohistochemistry

Internal Reference Standards techniques

Internal laboratory reference materials

Internal reference absorber

Internal reference compounds

Internal reference compounds table

Internal reference electrode

Internal reference principle

Internal reference redox scale

Internal reference rule

Internal reference standards

Internal reference, absolute configuration

Internal reference, absolute configuration determination

Internally contracted multi-reference

Internally contracted multi-reference configuration interaction

International Chemical Reference Substances

International Practical Temperature Scale secondary reference points

International Reference Life Cycle Data

International Reference Life Cycle Data System

International Reference Prices

International Reference Service

International Standardization Organization reference materials

Ionic solid state internal references

Metallic contacts, solid state internal references

Other Internal Reference Electrodes

Quality control — International Reference Materials

Quantifiable Internal Reference

Quantifiable Internal Reference Standards

Quantifiable Internal Reference Standards QIRS)

Quantifiable Internal Reference immunohistochemistry

Quantifiable Internal Reference standardization

Reference internal element, choice

Reference internal standard method

Solid state internal references

Statistics, morphology, abundance - using an internal reference

Tetramethylsilane internal reference

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