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Sample activity

Neutron Activation Ana.lysis, A measured sample activated by neutron bombardment emits gamma rays that are used to determine the mercury content by proton-spectmm scanning. Mercury concentrations as low as 0.05 ppb have been determined by this method. [Pg.108]

Since the catalyst is so important to the cracking operation, its activity, selectivity, and other important properties should be measured. A variety of fixed or fluidized bed tests have been used, in which standard feedstocks are cracked over plant catalysts and the results compared with those for standard samples. Activity is expressed as conversion, yield of gasoline, or as relative activity. Selectivity is expressed in terms of carbon producing factor (CPF) and gas producing factor (GPF). These may be related to catalyst addition rates, surface area, and metals contamination from feedstocks. [Pg.17]

The requirement may not apply to all product acceptance decisions. If your acceptance of the end product does not depend upon acceptance decisions being made on its component parts, any sampling carried out on receipt inspection or in-process is not important to the product acceptance decision and can therefore be ignored in your documented quality system. This is a wise course of action if you can be sure this will always be the case but if you can t, and more often than not you won t know, it is prudent to encompass a//sampling activities in your quality system. [Pg.547]

The actual amt of Na and K in solid proplnt samples is calcd by comparing the sample activity with the activity of a ref sample with known concns of Na and K. In this case, the ref standards consisted of water samples doped with known amts of Na and K, with all other conditions being the same as for the proplnt samples... [Pg.363]

Send message to SAMPLE activate procedure find polarity ... [Pg.639]

Active Air Sampling Active air sampling provides quantitative data because air at a known flow rate is impacted on a strip of nutrient media, followed by incubation of the nutrient strips and enumeration of colonies. Common active air sampling instruments include the slit-to-agar impact sampler and the centrifugal (Reuter) sampler. [Pg.414]

Figure 2. FTIR spectra of CO (30 Torr) adsorbed at rt on Pt/H-MCM-22 sample calcined at 500°C (A) and at 300°C (B). Curves a) are referred to samples activated in 02 flow at 500°C for 2h, while curves b) were collected after treatment in air at 800°C for 1,5h. Figure 2. FTIR spectra of CO (30 Torr) adsorbed at rt on Pt/H-MCM-22 sample calcined at 500°C (A) and at 300°C (B). Curves a) are referred to samples activated in 02 flow at 500°C for 2h, while curves b) were collected after treatment in air at 800°C for 1,5h.
Figure 7.7 Schematic set-up for measuring X-ray fluorescence with an energy-dispersive detector as in EDX. Irradiation of a bulk sample activates a pear-shaped volume from which X-rays are emitted. The chance of secondary processes is considerable and requires correction of the measured X-ray yields secondary effects are much less important if the sample is a thin film. Figure 7.7 Schematic set-up for measuring X-ray fluorescence with an energy-dispersive detector as in EDX. Irradiation of a bulk sample activates a pear-shaped volume from which X-rays are emitted. The chance of secondary processes is considerable and requires correction of the measured X-ray yields secondary effects are much less important if the sample is a thin film.
Numerous sampling activities have been conducted in Iowa, Kansas, Nebraska, and Missouri since the initial detection of carbon tetrachloride at Waverly. [Pg.108]

Sampling activities are important because if the sample does not represent what it is intended to represent, all operations that follow, whether they are wet or instrumental methods, will not give a reliable result. Sample preparation schemes are important because if the sample is not prepared properly for the method chosen, the method, whether wet or instrumental, again will not give a reliable result. [Pg.515]

The design and construction of sample collection and field test kits is a planning activity, since these kits must be ready to go at a moment s notice in response to a possible contamination threat. In addition to improving the efficacy of the site characterization and sampling activities, advance preparation of sample collection and field test kits offers several advantages ... [Pg.111]

Because of the diversity of potential field testing and sampling activities during the characterization, there may be no specific quality assurance (QA) activities that apply to all sampling procedures. However, the following general QA principles would apply in most cases and are consistent with the QA guidelines published by USEPA s Environmental Response Team ... [Pg.112]

The collection of physical evidence is not generally considered time sensitive however, site characterization and sampling activities are time sensitive due to the public health implications of contaminated environmental media air, water, and/or soil. Thus, collection of environmental media samples may precede collection of physical evidence, and care must be taken not to disturb the crime scene while performing these activities. If samples can be collected outside of the boundaries of the suspected crime scene, this may avoid concerns about the integrity of the crime scene. [Pg.113]

Petroleum products have a vast array of uses. In approximate order of importance the uses are as fuels for vehicles and industry, as heating oils, as lubricants, as raw materials in manufacturing petrochemicals and pharmaceuticals, and as solvents. By a wide margin, most products derived from petroleum find use as fossil fuels to run vehicles, to produce electricity, and to heat homes and business. About 65% of the petroleum used as fuel is consumed as gasoline in automobiles. Thus, petroleum products are ubiquitous in the modem environment, which leads to contamination problems for both the environment and in sampling activities. [Pg.18]

When using standard solutions prepared on the basis of activities calculated from these activity scales, and provided there is no interfierence and that the prelogarithmic term in the E versus log a dependence is Nernstian or at least accurately known and constant, the sample activity can be determined from the ISE potentials obtained in the sample and in a standard solution (see (4.13), p. 74-6). [Pg.101]

Cu-A1MCM-41 samples, activated as above, possess Cu2 , Cu , and Cu2 0 species Cu2 cations are easier reduced if NbMCM-41 matrix is applied. [Pg.821]


See other pages where Sample activity is mentioned: [Pg.524]    [Pg.133]    [Pg.683]    [Pg.440]    [Pg.682]    [Pg.152]    [Pg.163]    [Pg.979]    [Pg.191]    [Pg.97]    [Pg.159]    [Pg.107]    [Pg.110]    [Pg.628]    [Pg.110]    [Pg.57]    [Pg.262]    [Pg.237]    [Pg.70]    [Pg.139]    [Pg.49]    [Pg.53]    [Pg.54]    [Pg.149]    [Pg.377]    [Pg.42]    [Pg.342]    [Pg.299]    [Pg.277]    [Pg.35]    [Pg.354]    [Pg.114]    [Pg.115]   


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Active sampling

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