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Sample conditioning

Although additional sample handling between purification steps should be avoided, it may be necessary to adjust the buffer conditions of an eluted product (pH, ionic strength and/or buffering ions) to ensure compatibility with the following purification technique. [Pg.26]

Buffer exchange of mouse plasma on HiPrep 26/10 Desalting. [Pg.26]

Use pre-packed columns of Sephadex G-25 for rapid sample conditioning at laboratory scale, as shown in Table 5. [Pg.26]

Pre-packed column Sample volume loading per run Sample volume recovery per run Code No. [Pg.26]

For fast group separations between high and low molecular weight substances. [Pg.27]

Before a sample can be analyzed it is necessary to remove contaminating materials which can alter the surface potential and block or fill pores. Sample conditioning can be accomplished by vacuum pumping or [Pg.144]

Dotted line is gas flow through sample cell. Signal meter is shown at bottom. [Pg.145]

When a vacuum is used to outgas, precautions must be taken to prevent the initial surge from blowing powder throughout the system. In a well-sealed system outgassing can be taken as completed when no pressure increase can be detected after isolation from the pump. For routine work generally 10 to 10 torr (mm of mercury) is sufficient. The usual precautions, such as a baffle and a cold trap, should be taken to ensure no contamination by the pump oil. [Pg.146]


Fig. 2. Cellulose acetate stress—strain properties at standard and wet conditions, tested at 60% min extension rate, 3.9 cm gauge length. Sample conditions standard, 21°C, 65% rh wet, 21°C, water wet. To convert N/tex to gf/den, multiply by 11.33. Fig. 2. Cellulose acetate stress—strain properties at standard and wet conditions, tested at 60% min extension rate, 3.9 cm gauge length. Sample conditions standard, 21°C, 65% rh wet, 21°C, water wet. To convert N/tex to gf/den, multiply by 11.33.
The objective ia any analytical procedure is to determine the composition of the sample (speciation) and the amounts of different species present (quantification). Spectroscopic techniques can both identify and quantify ia a single measurement. A wide range of compounds can be detected with high specificity, even ia multicomponent mixtures. Many spectroscopic methods are noninvasive, involving no sample collection, pretreatment, or contamination (see Nondestructive evaluation). Because only optical access to the sample is needed, instmments can be remotely situated for environmental and process monitoring (see Analytical METHODS Process control). Spectroscopy provides rapid real-time results, and is easily adaptable to continuous long-term monitoring. Spectra also carry information on sample conditions such as temperature and pressure. [Pg.310]

Dynamics of Process Measurements Especially where the measurement device is incorporated into a closed loop control configuration, dynamics are important. The dynamic characteristics depend on the nature of the measurement device, and also on the nature of components associated with the measurement device (for example, thermowells and sample conditioning equipment). The term mea-.sui ement system designates the measurement device and its associated components. [Pg.758]

Where the manufacturer of the measurement device does not supply the associated eqiiipment (thermowells, sample conditioning equipment, and the like), the user must incorporate the characteristics of these components to obtain the dynamics of the measurement system. [Pg.758]

Modern transducers and microprocessors have been used successfully to automate particulate sampling trains in order to eliminate the operating curves and manual adjustments (7). The automated samplers adjust continuously to maintain isokinetic conditions. In addition, the microprocessor continuously calculates and displays both instantaneous sampling conditions and the total sample volume collected at any given moment. The use of the automated system with the microprocessor, therefore, eliminates both operator and calculation errors. [Pg.544]

Plastics will continue to be required in space applications from rockets to vehicles for landing on other planets. The space structures, reentry vehicles, and equipment such as antennas, sensors, and an astronaut s personal communication equipment that must operate outside the confines of a spaceship will encounter bizarre environments. Temperature extremes, thermal stresses, micrometeorites, and solar radiation are sample conditions that are being encountered successfully that include the use of plastics. [Pg.108]

However, some of the conditions in the alpha ion source do differ significantly from those in conventional ion-molecule sources. The most important difference is caused by the absence of an electric field and the mode of sampling. Positive and negative particles are carried out by mass flow. Therefore it is necessary to understand the reaction and sampling conditions at least qualitatively. For this reason we are devoting this section to a description of the conditions and a discussion of some experiments which were done specifically to obtain a better understanding of the sample prehistory. [Pg.218]

A Simple Model for the Reaction and Sampling Conditions. A model proposed to represent the sampling conditions is shown in... [Pg.221]

Figure 4. Sampling conditions at 20 torr most of the ionic sample originates from a volume of approximately 1-mm. radius electrons are collected much less efficiently... Figure 4. Sampling conditions at 20 torr most of the ionic sample originates from a volume of approximately 1-mm. radius electrons are collected much less efficiently...
A simple order of magnitude estimate of the rate constants for reaction with ethylene can be made for the high intensity ions in the 5-torr spectrum. Since the average reaction time, limited by neutralization or removal from the ion source is a few milliseconds (see section dealing with sampling conditions and section on ethylene in xenon) we can take 1 msec, as the half-life of these ions in 5-torr ethylene. This leads to k = 10-14 to 10-15 cc. molecule-1 sec.-1 as a rate constant for further reaction with ethylene. The value for 5a found by the kinetic treatment above was 8 X 10 -14. [Pg.244]

For each sample, condition Cig SPE (6-cc/l-g) cartridges with 6mL of methanol and 3 x 6mL of 0.005% aqueous H3PO4 in 10% MeOH-HaO. Stop Flow as the solution reaches the top of the sorbent (the SPE sorbent must not be allowed to go... [Pg.1182]

Figure A2.1 Waters ProMonix On-Line HPLC analyzer. The upper compartment door contains a keypad for programming and operation of the analyzer. The upper window allows viewing of indicator lights and a liquid crystal display that provides the operator with analyzer interface, programmed parameters, and instrument status results. The lower chamber contains the pumps, valves, injector, and detector(s) required for the chromatographic separation. The sample conditioning plate for online process monitoring is to the right of the analyzer. This is a typical process HPLC. (From Cotter, R.L. and Li, J.B., Lab Rob Autom., 1, 251,1989. With permission of VCH Publishers.)... Figure A2.1 Waters ProMonix On-Line HPLC analyzer. The upper compartment door contains a keypad for programming and operation of the analyzer. The upper window allows viewing of indicator lights and a liquid crystal display that provides the operator with analyzer interface, programmed parameters, and instrument status results. The lower chamber contains the pumps, valves, injector, and detector(s) required for the chromatographic separation. The sample conditioning plate for online process monitoring is to the right of the analyzer. This is a typical process HPLC. (From Cotter, R.L. and Li, J.B., Lab Rob Autom., 1, 251,1989. With permission of VCH Publishers.)...
Taking into consideration that antenna xanthophylls not only possess original absorption but also resonance Raman spectra, and the fact that the Raman signal is virtually free from vibrational spectroscopy artifacts (water, sample condition, etc.), it seemed of obvious advantage to apply the described combination of spectroscopies for the identification of these pigments. [Pg.121]

Probability that the analyte A is present in the test sample Conditional probability probability of an event B on the condition that another event A occurs Probability that the analyte A is present in the test sample if a test result T is positive Score matrix (of principal component analysis)... [Pg.14]

Reference Sample Condition Antigen Retrieval IHC (IP) Results... [Pg.28]

Samples conditioned to ambient room temperature and humidity. [Pg.295]


See other pages where Sample conditioning is mentioned: [Pg.91]    [Pg.66]    [Pg.716]    [Pg.767]    [Pg.188]    [Pg.496]    [Pg.163]    [Pg.164]    [Pg.218]    [Pg.226]    [Pg.242]    [Pg.41]    [Pg.277]    [Pg.357]    [Pg.145]    [Pg.425]    [Pg.93]    [Pg.91]    [Pg.130]    [Pg.321]    [Pg.139]    [Pg.139]    [Pg.63]    [Pg.532]    [Pg.98]    [Pg.141]    [Pg.60]    [Pg.372]    [Pg.407]    [Pg.502]    [Pg.102]    [Pg.43]   
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Bulk Measurement, Sampling, Conditioning, and Shipment of Safeguards Inspection Samples

Catalysis sample condition

Catalyst samples preparation reaction conditions

Conditional Monte Carlo sampling

Conditional sampling

Conditional sampling

Conditioning of samples

Conditioning the Samples

Conditions of sample preparation

Conditions of sampling

Environmental sample conditions

Extraction conditions samples

Field sample conditions

Mass spectrometry sample conditioning

Online sample conditioning

Optimal Sample Storage Conditions

Prediction of Branched Architectures by Conditional Monte Carlo Sampling

Sample Collection and Conditioning

Sample Condition

Sample Preparation and Selection of HPLC Operating Conditions

Sample Prepared Under Equilibrium Conditions Prior to Spin Column Treatment

Sample Solutions for Isothermal Operating Conditions

Sampling of initial conditions

Scanning sample conditions

Techniques of Sample Preparation and Conditioning

Transmission sample conditions

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