Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Measurement methods effect

When designing and evaluating an analytical method, we usually make three separate considerations of experimental error. First, before beginning an analysis, errors associated with each measurement are evaluated to ensure that their cumulative effect will not limit the utility of the analysis. Errors known or believed to affect the result can then be minimized. Second, during the analysis the measurement process is monitored, ensuring that it remains under control. Finally, at the end of the analysis the quality of the measurements and the result are evaluated and compared with the original design criteria. This chapter is an introduction to the sources and evaluation of errors in analytical measurements, the effect of measurement error on the result of an analysis, and the statistical analysis of data. [Pg.53]

The superpositioning of experimental and theoretical curves to evaluate a characteristic time is reminiscent of the time-tefnperature superpositioning described in Sec. 4.10. This parallel is even more apparent if the theoretical curve is drawn on a logarithmic scale, in which case the distance by which the curve has to be shifted measures log r. Note that the limiting values of the ordinate in Fig. 6.6 correspond to the limits described in Eqs. (6.46) and (6.47). Because this method effectively averages over both the buildup and the decay phases of radical concentration, it affords an experimentally less demanding method for the determination of r than alternative methods which utilize either the buildup or the decay portions of the non-stationary-state free-radical concentration. [Pg.379]

Normalization is a preprocessing method often appHed to spectral data. It makes the lengths of all of the data vectors the same. Thus the sum of the squares of the elements of the data vectors is constant for all samples in the set. If is this sum for the unnormalized sample /, then to normalize the data vectors to the constant m, each element of the data vector would be multiphed by vnj.yj. A common example of this method is normalizing the area under a set of curves to unit area. AppHcation of this method effectively removes the variance in a data set because of arbitrary differences in magnitudes of a set of measurements when such variation is not meaningful and would obscure the significant variance. [Pg.419]

Ruthven (gen. refs.) summarizes methods for the measurement of effective pore diffusivities that can be used to obtain tortuosity factors by comparison with the estimated pore diffusion coefficient of the adsorbate. Molecular diffusivities can be estimated with the methods in Sec. 6. [Pg.1511]

The measured diameters of particles shoiild as nearly as possible represent the effective particle size of a dust as it exists in the gas stream. When significant flocculation exists, it is sometimes possible to use measurement methods based on gravity settling. [Pg.1582]

The goals of the F EI are to raise awareness of loss potential and identify ways to reduce potential severity and potential dollar loss in a cost-effective manner. TLe index number has significance as a comparison and in calculations to estimate the maximum probable property damage (MPPD). It also provides a method for measuring tbe effect of outage (plant being shut down) on the business. It is easy for users to get credible results with a small amount of training. [Pg.2273]

In this work hybrid method is suggested to determine anionic surfactants in waters. It is based on preconcentration of anionic surfactants as their ion associates with cationic dyes on the membrane filter and measurement of colour intensity by solid-phase spectrophotometry method. Effect of different basic dyes, nature and hydrophobicity of anionic surfactants, size of membrane filter pores, filtration rate on sensitivity of their determination was studied. Various cationic dyes, such as Methylene Blue, Crystal Violet, Malachite Green, Rhodamine 6G, Safranin T, Acridine Yellow were used as counter ions. The difference in reflection between the blank and the sample was significant when Crystal Violet or Rhodamine 6G or Acridine Yellow were used. [Pg.267]

Measure of averaging time Cyclic factor measured Measurement method with same averaging time Effect with same averaging time... [Pg.47]

Develop methods to measure the effectiveness of inherent safety efforts and to provide feedback to personnel to improve performance. [Pg.112]

Where you devise original solutions to the measurement of characteristics the theory and development of the method should be documented and retained as evidence of the validity of the measurement method. Any new measurement methods should be proven by rigorous experiment to detect the measurement uncertainty and cumulative effect of the errors in each measurement process. The samples used for proving the method should also be retained so as to provide a means of repeating the measurements should it prove necessary. [Pg.407]

The effective length is defined as the measured center distance plus the outside circumference of one of the inspection pulleys. This measurement method accounts for the modulus of elasticity, or stretch ability, and dimensional variations among belts with the same cross-section. [Pg.971]

Recently, there has been a growth of interest in the development of in vitro methods for measuring toxic effects of chemicals on the central nervous system. One approach has been to conduct electrophysiological measurements on slices of the hippocampus and other brain tissues (Noraberg 2004, Kohling et al. 2005). An example of this approach is the extracellular recording of evoked potentials from neocortical slices of rodents and humans (Kohling et al. 2005). This method, which employs a three-dimensional microelectrode array, can demonstrate a loss of evoked potential after treatment of brain tissue with the neurotoxin trimethyltin. Apart from the potential of in vitro methods such as this as biomarkers, there is considerable interest in the use of them as alternative methods in the risk assessment of chemicals, a point that will be returned to in Section 16.8. [Pg.305]

Outcome measurement is not discussed further in this chapter, hut it should he emphasized that some distinctive contributions could be made by economics. These include the development of summary unidimensional measures (discussed in the cost-utility section earlier), and benefit valuation in monetary terms (with its attendant difficulties, even though valuation methods are breaking new ground). However, acceptable (and potentially insightful) economic evaluations can be conducted without resorting to utility or benefit measurement. Cost-effectiveness and cost-consequences approaches have a lot to offer, building on outcome measures which will be more familiar to non-economist researchers in the field. It is for this reason that cost-effectiveness and cost-consequences analyses, linked to drug trials, are the most likely to be used over the next few years. [Pg.15]

The cancellation of gas phase spectral features using the "half plate design Is far superior to methods Involving a second gas cell placed In the reference beam. This Is because the gas density and Its rotational state population will differ In the two cells for different sample (and therefore gas) temperatures. For high sensitivity measurements, these effects can be difficult to handle using two cells. [Pg.407]

An infrequently used method (in pharmaceutical research) for determining the UWL permeability involves measuring transport of molecules across a high-porosity microfilter that is not coated by a lipid. The molecules are able to diffuse freely in the water channels of the microfilter. The filter barrier prevents convective mixing between the donor and acceptor sides, and an UWL forms on each sides of the microfilter. Camenisch et al. [546] measured the effective permeabilities of a series of drug molecules in 96-well microtiter plate-filterplate (Millipore GVHP mixed cellulose ester, 0.22 pm pore) sandwich where the filters were not coated by a lipid. The permeabilities were nearly the same for all the molecules, as shown in Fig. 7.8a. Our analysis of their data, Fig. 7.8b, indicates / aq = 460 pm (sandwich stirred at 150 rpm). We have been able to confirm similar results in our laboratory with different microfilters, using the lipid-free method. [Pg.207]

A new experimental method has been introduced to measure the effect of the crystal anapole moment on p decay. The basic hypothesis is very similar to that assumed by Zel dovich. The special idea is to introduce the description of solid-state physics (crystallography) into the process of weak interaction. The p decay rate will be modified due to the presence of crystal anapole moment. If this modification could be detected, the hypothesis for the anapole moment and its coupling to weak interaction will be verified for the first time if this modification could not be detected by this method, an upper limit of up to 1(T6 for the coupling of anapole moment to weak process should be given. This experiment will give direct verification to Zel dovich s assumption. [Pg.313]

As may be seen from Figure 3, first order plots based on the conversions obtained by both methods were linear with slopes in close agreement. The apparent rate constant is 0.57 h"1 based on H2 evolution and 0.54 h"1 based on the formation of glycine salt thereby indicating that it is valid to use the simpler H2 evolution measurements when measuring the effects of process variables on the reaction. [Pg.30]

The effects of cytoplasmic viscosity are widely unexplored. This may be attributed to the relatively difficult measurement methods available. In the cytoplasm, magnetic microparticles were predominantly used to obtain information on viscoelastic properties [125-127]. Clearly, the use of magnetic microparticles demands the use of very expensive equipment the observation of the particles is time-consuming, thus limiting temporal resolution, and the interaction between the particles and the cellular environment may also cause measurement artifacts. [Pg.295]

As pointed out in the first part of this work, tetrafunctionally crosslinked PDMS also shows some dependence of the energy part of the modulus on network density and on the measuring method, but the effects observed there, are much smaller than the great variation of /a with branching density in case of networks... [Pg.320]

In order to focus on more of the basic research problems related to radon, a symposium was organized in conjunction with the 191th National Meeting of the American Chemical Society. This volume presents most of the reports given at that symposium. There are five major groups of reports occurrence, measurement methods, physical and chemical properties of radon and its decay products, health effects, and mitigation of radon levels. [Pg.8]

On other hand, we found a good correlation between the results by the present method and those by the Terradex detector. However, the mean value obtained by the Terradex detector were about twice those by the present method. The reasons for this significant difference are unknown and may be due to errors in the calibration experiments and in the conditions during the measurements. In the calibration experiments the effect of existence of thoron in the chambers could be one of the reasons. As regards the condition in the measurements, methods for subtraction of background tracks and deposition of dust onto the bare detector could be candidates. However, we do not have enough data to determine the reasons for some of this difference. [Pg.188]

Most studies of the physical binding of hydrocarbon metabolites and metabolite model compounds have measured the effect of DNA binding on hydrocarbon fluorescence intensities, fluorescence lifetimes and UV absorption spectra Radioactive labelling has also been used, but less frequently. Spectroscopic methods are particularly convenient. These methods, especially fluorescence methods, are also very sensitive. All of the hydrocarbons in Figure 1 except the epoxides have high fluorescence quantum yields, which permit routine detection in the 10 -10 7 M concentration range. [Pg.220]


See other pages where Measurement methods effect is mentioned: [Pg.1541]    [Pg.1911]    [Pg.713]    [Pg.124]    [Pg.461]    [Pg.524]    [Pg.149]    [Pg.555]    [Pg.225]    [Pg.190]    [Pg.584]    [Pg.585]    [Pg.90]    [Pg.311]    [Pg.370]    [Pg.27]    [Pg.301]    [Pg.53]    [Pg.2]    [Pg.435]    [Pg.178]    [Pg.75]    [Pg.160]    [Pg.204]    [Pg.53]    [Pg.132]    [Pg.72]   


SEARCH



Effect measure

© 2024 chempedia.info