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Books on the topic 'Flow rate measurement'

Author: Grafiati

Published: 4 June 2021

Last updated: 29 May 2022

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1

Kremlevskiĭ, P. P. Flow rate measurement in multiphase flows. New York: Begell House, 1999.

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2

Parchure, T. M. High-accuracy flow rate measurement for water supply and dredged slurry transport pipelines. Vicksburg, Miss: U.S. Army Engineer Waterways Experiment Station, 1997.

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3

Trimmer, Walter L. Estimating water flow rates. [Corvallis, Or.]: Oregon State University Extension Service, 1991.

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4

Kremlevskii, P. P. Flow Rate Measurement in Multiphase Flows. 2nd ed. Hemisphere Pub, 1996.

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5

Kremlevsky, P. P. Flow Rate Measurement in Multiphase Flows (SCME). Taylor & Francis Inc, 1999.

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6

Stankovic, Violeta. Mass flow rate measurement in pneumatic conveyors. Bradford, 1986.

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7

Center, Lewis Research, ed. Semiempirical method of determining flow coefficients for pitot rake mass flow rate measurements. [Cleveland, Ohio: National Aeronautics and Space Administration, Lewis Research Center, 1985.

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8

Harry, Johnson, Margasahayam Ravi, and United States. National Aeronautics and Space Administration., eds. Nonintrusive flow rate determination through space shuttle water coolant loop floodlight coldplate. Kennedy Space Center, Fla: National Aeronautics and Space Administration, John F. Kennedy Space Center, 1997.

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9

F, Chao David, and NASA Glenn Research Center, eds. Flow visualization in evaporating liquid drops and measurement of dynamic contact angles and spreading rate. Cleveland, Ohio: National Aeronautics and Space Administration, Glenn Research Center, 2001.

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10

IGEM. Flow Rate Exceeding 6 M3 H-1 and Inlet Pressure Not Exceeding 38 Bar (Gas Measurement Procedures S.). Institution of Gas Engineers and Managers, 2005.

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11

[Flight and static exhaust flow properties of an F110-GE-129 engine in an F-16XL airplane during acoustic tests]. [Edwards, Calif: NASA Dryden Flight Research Center, 1996.

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12

Enweluzor, Michael P. C. Instrument for solids mass flow measurement in pneumatic conveyors: Investigation of conveying velocity, mass flow rate and static pressure gradient relationships. Design and evaluation of microprocessor based mass flocumeter combining differential pressure sensing with transit time correlation velocity measurement. Bradford, 1986.

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13

Lighton, John R. B. Measuring Metabolic Rates. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198830399.001.0001.

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Measuring Metabolic Rates demystifies the field of metabolic rate measurement, explaining every common variation of the art, from century-old manometric methods through ingenious syringe-based techniques, direct calorimetry, aquatic respirometry, stable-isotope metabolic measurement, and every type of flow-through respirometry. Each variation is described in enough detail to allow it to be applied in practice. Special chapters are devoted to metabolic phenotyping and human metabolic measurement, including room calorimetry. Background information on different analyzer and equipment types allows users to choose the best instruments for their application. Respirometry equations—normally a topic of terror and confusion to researchers—are derived and described in enough detail to make their selection and use effortless. Tools and skills—many of them open source—that will amplify the innovative researcher’s capabilities are described. Vital topics such as manual and automated baselining, implementing multi-animal systems, common pitfalls, and the correct analysis and presentation of metabolic data are covered in enough detail to turn a respirometry neophyte into a hardened metabolic warrior, ready to take on the task of publication in peer-reviewed journals with confidence.

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14

M, Stubbs Sandy, and United States. National Aeronautics and Space Administration. Scientific and Technical Information Office., eds. Measurements of flow rate and trajectory of aircraft tire-generated water spray. [Washington, D.C.]: National Aeronautics and Space Administration, Scientific and Technical Information Office, 1987.

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15

Dussaule, Jean-Claude, Martin Flamant, and Christos Chatziantoniou. Function of the normal glomerulus. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0044_update_001.

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Glomerular filtration, the first step leading to the formation of primitive urine, is a passive phenomenon. The composition of this primitive urine is the consequence of the ultrafiltration of plasma depending on renal blood flow, on hydrostatic pressure of glomerular capillary, and on glomerular coefficient of ultrafiltration. Glomerular filtration rate (GFR) can be precisely measured by the calculation of the clearance of freely filtrated exogenous substances that are neither metabolized nor reabsorbed nor secreted by tubules: its mean value is 125 mL/min/1.73 m² in men and 110 mL/min/1.73 m² in women, which represents 20% of renal blood flow. In clinical practice, estimates of GFR are obtained by the measurement of creatininaemia followed by the application of various equations (MDRD or CKD-EPI) and more recently by the measurement of plasmatic C-cystatin. Under physiological conditions, GFR is a stable parameter that is regulated by the intrinsic vascular and tubular autoregulation, by the balance between paracrine and endocrine agents acting as vasoconstrictors and vasodilators, and by the effects of renal sympathetic nerves. The mechanisms controlling GFR regulation are complex. This is due to the variety of vasoactive agents and their targets, and multiple interactions between them. Nevertheless, the relative stability of GFR during important variations of systemic haemodynamics and volaemia is due to three major operating mechanisms: autoregulation of the afferent arteriolar resistance, local synthesis and action of angiotensin II, and the sensitivity of renal resistance vessels to respond to NO release.

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16

Sklar, Larry A., ed. Flow Cytometry for Biotechnology. Oxford University Press, 2005. http://dx.doi.org/10.1093/oso/9780195183146.001.0001.

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Flow cytometry is a sensitive and quantitative platform for the measurement of particle fluorescence. In flow cytometry, the particles in a sample flow in single file through a focused laser beam at rates of hundreds to thousands of particles per second. During the time each particle is in the laser beam, on the order of ten microseconds, one or more fluorescent dyes associated with that particle are excited. The fluorescence emitted from each particle is collected through a microscope objective, spectrally filtered, and detected with photomultiplier tubes. Flow cytometry is uniquely capable of the precise and quantitative molecular analysis of genomic sequence information, interactions between purified biomolecules and cellular function. Combined with automated sample handling for increased sample throughput, these features make flow cytometry a versatile platform with applications at many stages of drug discovery. Traditionally, the particles studied are cells, especially blood cells; flow cytometry is used extensively in immunology. This volume shows how flow cytometry is integrated into modern biotechnology, dealing with issues of throughput, content, sensitivity, and high throughput informatics with applications in genomics, proteomics and protein-protein interactions, drug discovery, vaccine development, plant and reproductive biology, pharmacology and toxicology, cell-cell interactions and protein engineering.

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17

Nixon, Patricia A. Pulmonary function. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199232482.003.0006.

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The focus of this chapter is the assessment and interpretation of pulmonary function during exercise in children, with emphasis on the parameters commonly measured in the paediatric setting. The measurements of resting pulmonary function (i.e. lung volumes and expiratory flow rates) are presented to provide the basic foundation for understanding changes that occur with exercise. Some measurements are more relevant to children with cardiopulmonary disorders, and examples of normal and abnormal responses are provided. In some instances, data on children are lacking, so responses of adults are presented.

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18

Georgia Tech Research Institute. Electro-optics and Environmental Materials Laboratory. and United States. National Aeronautics and Space Administration., eds. The measurement of sulfur oxidation products and their role in homogeneous nucleation: NASA gant no. NAGW-4692, Georgia Tech Project no. A-5036; final report, July 1, 1995-June 30, 1997. [Washington, DC: National Aeronautics and Space Administration, 1997.

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19

Orenbuch-Harroch, Efrat, and Charles L. Sprung. Pulmonary artery catheterization in the ICU. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0133.

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Haemodynamic monitoring is a significant component in the management of critically-ill patients. Flow-directed pulmonary artery catheters (PAC) are a simple and rapid technique for measuring several continuous or intermittent circulatory variables. The PAC is helpful in diagnosis, guidance of therapy, and monitoring therapeutic interventions in various clinical conditions, including myocardial infarction and its complications, non-cardiogenic pulmonary oedema and severely ill patients.The catheter is inserted through a large vein. The PAC is advanced, after ballooninflation with 1.5 mL of air, through the right ventricle across the pulmonary valve and into the pulmonary artery (PA). Finally, the catheter is advanced to the ‘wedge’ position. The pulmonary artery wedge pressure (PAWP) is identified by a decrease in pressure combined with a characteristic change in the waveform. The balloon should then be deflated and the PA tracing should reappear. Direct measurements include central venous pressure, pulmonary artery pressure, and PAWP, which during diastole represents the left ventricular end-diastolic pressure and reflects left ventricular preload. Cardiac output can be measured by thermodilution technique. Other haemodynamic variables can be derived from these measurements. Absolute contraindications are rare. Relative contraindications include coagulopathy and conditions that increase the risk of arrhythmias.

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20

Kinnear, William, and James H. Hull. A Practical Guide to the Interpretation of Cardiopulmonary Exercise Tests. 2nd ed. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780198834397.001.0001.

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A Practical Guide to the Interpretation of Cardiopulmonary Exercise Tests is a short, but comprehensive, guide for those who are involved in the supervision of exercise tests and interpretation of cardiopulmonary exercise test (CPET) data. It is a clear and concise guide which will also be of interest to those who request CPETs and who wish to understand more about how to use the results. The first four chapters cover the reasons why a CPET may be requested, pre-test assessment, supervision of the test to ensure that it is safe, and the practicalities of the test itself. Subsequent chapters look in detail at the key CPET measurements of heart rate, ventilation, oxygen uptake, and carbon dioxide output. There are chapters on the parameters that can be derived from these basic measurements: ventilatory equivalents, oxygen pulse, and the respiratory exchange ratio. Further chapters show how the anaerobic threshold and respiratory compensation point are obtained, and how they can be used to interpret the physiological response to exercise. The role of monitoring oxygen saturation and flow–volume loops during the test is described. The third section of the book has chapters on presentation of results, interpretative strategies, and summaries of classical CPET patterns seen in different diseases. The final chapters consider the role of preoperative CPET testing and how to prescribe exercise. All chapters have pointers to further resources.

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21

L, Lawing Pierce, and Langley Research Center, eds. Measurements in the flow field of a cylinder with a laser transit anemometer and a drag rake in the Langley 0.3 m Transonic Cryogenic Tunnel. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1985.

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