Measuring tool

The corrosion inspection and wall thickness measurement of pipes was performed in the classical way both on film and on the monitor using simple software measuring tools. Additionally algorithms were developed for an interactive, computer supported evaluation. 

This procedure offers the possibiUty of remote noncontact velocity measurement, where no probes disturb the flow. It is thus compatible for use with hot or corrosive gases. Commercial laser velocimeters have become weU-developed measurement tools. Examples of laser velocimetry include remote measurement of wind velocity, measurement of vortex air flow near the wing tips of large aircraft, and in vivo measurement of the velocity of blood flow. 

One of the new trends in chemical analysis appeared in the last decade is that the miniaturization. It becomes apparent in the miniaturization of analytical devices, separation procedures, measuring tools, analyzing samples and as a consequent the term micro have appeared. Further development of this trend have led to transfer from the term micro to nano one (nanoparticles, nanofluides, nanoprobes, nanoelectrodes, nanotubes, nanoscale, nanobarcode, nanoelectrospray, nanoreactors, etc). Thereupon a nanoscale films produced by Langmuir-Blodgett (LB) technique are proposed for modifying of chemical sensors. 

PL measurements are generally nondestructive, and can be obtained in just about any configuration that allows some optically transparent access within several centimeters of the sample. This makes it adaptable as an in situ measurement tool. Little sample preparation is necessary other than to eliminate any contamination that may contribute its own luminescence. The sample may be in air, vacuum, or in any transparent, nonfluorescing medium. 

Example 1 Steering Tool Measurements—Tool Face, Deviation... 

Example 2 Steering Tool Measurements— Tool Face, Deviation, and Azimuth... 

The nurse may request that the patient evaluate the pain using a standardized pain scale measurement tool. The pain is rated using a scale of 1 to 10, with 10 being the most severe pain and 1 being the least discomfort. Failure to adequately assess pain is a major factor in the undertreatment of pain. 

One of the main determinants of the number of subjects required to reach the desired statistical power is the precision of the measurement tool utilized. More precise measurements will reduce the number of subjects required. As an example, if a study is being conducted to assess the influence of a dietary supplement on body fat, several measurement tools could be used to assess this outcome. These tools range from low levels of cost and precision (e.g. skinfold measurements) to moderate levels (e.g. bioelectrical impedance) to high levels of cost and precision (dual x-ray absorptiometry - DXA). A study that uses skinfold measurements to measure the outcome will require many more subjects than one which employs DXA. Therefore, it is often less expensive in total to utilize a more expensive measurement tool, because the more precise tool will allow the study to have sufficient power with a smaller number of subjects. 

Clinical trials are costly to conduct, and results are often critical to the commercial viability of a phytochemical product. Seemingly minor decisions, such as which measurement tool to use or a single entry criterion, can produce thousands of dollars in additional costs. Likewise, a great deal of time, effort and money can be saved by having experts review the study protocol to provide feedback regarding ways to improve efficiency, reduce subject burden and insure that the objectives are being met in the most scientifically sound and cost-effective manner possible. In particular, I recommend that an expert statistician is consulted regarding sample size and power and that the assumptions used in these calculations are reviewed carefully with one or more clinicians. It is not uncommon to see two studies with very similar objectives, which vary by two-fold in the number of subjects under study. Often this can be explained by differences in the assumptions employed in the sample size calculations. 

One of the most interesting theorems of Worz et al. is that they see a serious potential for micro reactors to permit small-scale production of some different sort [110-112]. Micro channels serve as an ultra-precise measuring tool, whereas production is done in channels about 10 to 100 times larger, i.e. miUimeter-sized channels. The limit of tube diameter of industrial production reactors is reported to be 2 cm hence any new reactor of smaller characteristic dimensions bears some potential for improvement. Worz et al. conclude with the remark that the above strategy could be the most important result of their studies [110-112]. 

Innovation - advocates and opponents origin from microtechnology list of microfabrication techniques selectivity and efficiency as main driver for industrial implementation special properties and general advantages of micro reactors process-development issues BASF investigations on liquid/liquid and gas-phase reactions micro reactors as ideal measuring tools production in micro reactors as exception, the rule will be transfer to mm-sized channels [111],... 

Interview with Worz/BASF in a special on heat exchangers giving expert opinion on compact heat exchangers, feasibility and problems of large-scale implementation of micro reactors measuring tool for process optimization exotic status. scale-up unit-construction kit industrial implementation in 5 years [216],... 

All useful methods attempt to capture and describe all of the impacts during the entire life of the product or service from cradle to grave . This is the basis of the cluster of measurement tools known collectively as Life Cycle Assessment (LCA). 

This field is therefore at an exciting stage. Ion-selective electrodes have a proven track record in terms of clinical and biomedical analysis, with a well-developed theory and a solid history of fundamental research and practical applications. With novel directions in achieving extremely low detection limits and instrumental control of the ion extraction process this field has the opportunity to give rise to many new bioana-lytical measurement tools that may be truly useful in practical chemical analysis. 

Sources of Error 1. Experimental error in measurement 2. Measuring tools not reliable or not sensitive enough 3. Activity of ions as proposed by Debye and Huckel which states an effective concentration called activity which takes into account interionic attractions resulting in a decrease in the magnitude of colligative properties, especially for concentrated solutions. 

Beyond playing a significant role as a measurement tool, audits provide the opportunity to share a set of fresh perspectives on areas where requirements have yet to be codified (e.g., process control procedures, management information systems, and maintenance programs). Audits also serve to indicate ongoing efforts to reexamine and reevaluate operations to further reduce operational risks and consequent liabilities (including property damage and business interruption). 

The measurement of changes of the surface potential Vo at the interface between an insulator and a solution is made possible by incorporating a thin film of that insulator in an electrolyte/insulator/silicon (EIS) structure. The surface potential of the silicon can be determined either by measuring the capacitance of the structure, or by fabricating a field effect transistor to measure the lateral current flow. In the latter case, the device is called an ion-sensitive field effect transistor (ISFET). Figure 1 shows a schematic representation of an ISFET structure. The first authors to suggest the application of ISFETs or EIS capacitors as a measurement tool to determine the surface potential of insulators were Schenck (15) and Cichos and Geidel (16). 

Particular measurement tools face further problems. FT-ICR will have to overcome ion-ion interferences at high concentrations. As noted above, LC-MS can be subject to matrix effects, such as the presence of nonvolatiles. 

The extent of corrosion or wear can be determined by measuring the remaining thickness and comparing it to the original thickness. The extent of distortion in deformed components and elongation of fractured components should be determined. Common machine shop measuring tools provide adequate accuracy. 

The integrated DLS device provides an example of a measurement tool tailored to nano-scale structure determination in fluids, e.g., polymers induced to form specific assemblies in selective solvents. There is, however, a critical need to understand the behavior of polymers and other interfacial modifiers at the interface of immiscible fluids, such as surfactants in oil-water mixtures. Typical measurement methods used to determine the interfacial tension in such mixtures tend to be time-consuming and had been described as a major barrier to systematic surveys of variable space in libraries of interfacial modifiers. Critical information relating to the behavior of such mixtures, for example, in the effective removal of soil from clothing, would be available simply by measuring interfacial tension (ILT ) for immiscible solutions with different droplet sizes, a variable not accessible by drop-volume or pendant drop techniques [107]. 

Dietary assessment workers consistently agree that after selection of the most appropriate measurement tool, accurate and representative nutrient data on food composition are required. 

The variability of hazardous air pollutants (HAPs) is an important factor in determining hnman exposure to such chemicals, and in designing HAP measurement programs. The factors that contribute to HAP variability in an urban area also affect their global impact. Temporal variation was the major contributor to HAP variability for 19 of the 39 frequently detected compounds (Spicer et al., 1996). In the future, more precise measurement tools will be available to determine HAPs. Open-path monitoring of the atmosphere using Fourier transform infrared spectrometry has recently become... 

Although such studies are in their early stages, this example clearly demonstrates that we have the measurement tools to investigate the complex interaction of hydrodynamics and chemical kinetics in the complex porous medium represented by a fixed bed. Looking to the future, we may expect experiments of this nature to demonstrate how a catalyst with intrinsic high selectivity can produce a far wider product distribution when operated in a fixed-bed environment as a result of the spatial heterogeneity in hydrodynamics and hence, for example, mass transfer characteristics between the inter-pellet space within the bed and the internal pore space of the catalyst. 

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