Rapid method

Gilson, M. K. Multiple-site titration and molecular modeling Two rapid methods for computing energies and forces for ionizable groups in proteins. Proteins Struct. Punct. Genet. 15 (1993) 266-282. 

Orengo C A and W R Taylor 1990. A Rapid Method of Protein Structure Alignment. ]oumal ofTheon Biolo y 147 517-551. 

The third method is of limited application and is used only in special cases, The second is the most accurate and rapid method, and is of considerable technical importance. The chemical method (described below), although less accurate than the polarimetric method, is of great value for the estimation of sugars in biological fluids. In fact, for such purposes, it is often to be preferred to the polarimetric method owing to the probable presence of other substances having high optical rotations. 

Ueno, K. Kina, K. Colloid Titration—A Rapid Method for the Determination of Charged Colloid, /. Chem. Educ. 

Description of Method. Creatine is an organic acid found in muscle tissue that supplies energy for muscle contractions. One of its metabolic products is creatinine, which is excreted in urine. Because the concentration of creatinine in urine and serum is an important indication of renal function, rapid methods for its analysis are clinically important. In this method the rate of reaction between creatinine and picrate in an alkaline medium is used to determine the concentration of creatinine in urine. Under the conditions of the analysis, the reaction is first-order in picrate, creatinine, and hydroxide. 

Since viscometer drainage times are typically on the order of a few hundred seconds, intrinsic viscosity experiments provide a rapid method for evaluating the molecular weight of a polymer. A limitation of the method is that the Mark-Houwink coefficients must be established for the particular system under consideration by calibration with samples of known molecular weight. The speed with which intrinsic viscosity determinations can be made offsets the need for prior calibration, especially when a particular polymer is going to be characterized routinely by this method. 

A rapid method to determine the calcium content of lead alloys is a Hquid-metal titration using lead—antimony (1%) (9). The end point is indicated by a gray oxide film pattern on the surface of a sohdifted sample of the metal when observed at a 45° angle to a light source. The basis for the titration is the reaction between calcium and antimony. The percentage of calcium in the sample can be calculated from the amount of antimony used. If additional calcium is needed in the alloy, the melt is sweetened with a lead—calcium (1 wt %) master alloy. 

Refractive Index. The refractometric value of sugar solutions is used as a rapid method for the approximate determination of the soHds content (also known as dry substance), because it is assumed that the nonsugars present have a similar influence on the refractive index as sucrose. Measurement is usually carried out on a Brix refractometer, which is graduated in percentage of sucrose on a wt/wt basis (g sucrose/100 g solution) according to ICUMSA tables of refractive index at 20.0°C and 589 nm. Tables are available that give mass fraction corrections to refractometric values at temperatures different from 20°C. 

In the 3M Water/Alcohol Drop Test (41), this test is designed to provide a simple, rapid method to assess the aqueous stain resistance of substrates treated with a protective finish. 

Figure 12-25 provides a rapid method of determining the pond-area requirements for a given coohng duty. Di and Do are the approaches to equilibrium for the entering and leaving water, °F V Js trie wind velocity, mFh product PQ represents the area of the pond surface, ft /(gal-min) of flowto thepond. The P factor assumes a pond with uniform flow, without turbulence, and with the water warmer than the air. 

The baseline level of COHb is—0.5% for most individuals. Uponexposure to elevated levels of atmospheric CO, the percentage of COHb will increase in a very predictable manner. Analytical techniques are available to measure COHb from <0.1 to >80% in the bloodstream, providing a very rapid method for defermining the total body burden. If elevated levels of CO are reduced, the percentage of COHb will decrease over a period of time. 

For each fold one searches for the best alignment of the target sequence that would be compatible with the fold the core should comprise hydrophobic residues and polar residues should be on the outside, predicted helical and strand regions should be aligned to corresponding secondary structure elements in the fold, and so on. In order to match a sequence alignment to a fold, Eisenberg developed a rapid method called the 3D profile method. The environment of each residue position in the known 3D structure is characterized on the basis of three properties (1) the area of the side chain that is buried by other protein atoms, (2) the fraction of side chain area that is covered by polar atoms, and (3) the secondary stmcture, which is classified in three states helix, sheet, and coil. The residue positions are rather arbitrarily divided into six classes by properties 1 and 2, which in combination with property 3 yields 18 environmental classes. This classification of environments enables a protein structure to be coded by a sequence in an 18-letter alphabet, in which each letter represents the environmental class of a residue position. 

A rapid method to estimate pump horsepower is by the following formula ... 

This method of chromatogram preservation has lost a great deal of its importance with the increasing perfection of photographic methods, particularly since true-colored, instant, paper and slide positives have become available. Photography is the more rapid method of documentation if suitable photographic equipment is available. 

Bujac, P.B. and Mullin, J.W., 1969. A rapid method for the measurement of crystal growth rates in a fluidised bed crystallizer. Symposium on Industrial Crystallization. London, 1969. Rugby Institution of Chemical Engineers, pp. 121-129. 

Finally, treating the A-oxide directly with Tebbe reagent provides a rapid method of introducing the 2-methyl substituent (57 58). 

D. Wu, M. Berua, G. Maier and J. Johnson, An automated multidimensional sa eening approach for rapid method development in high-performance liquid cliromatography , 7. Pharm. Biomed. Anal. 16 57-68 (1997). 

Figure 13.11 Column-switcliing RPLC trace of a surface water sample spiked with eight chlorophenoxyacid herbicides at the 0.5 p-g 1 level 1, 2,4-dichlorophenoxyacetic acid 2, 4-chloro-2-methylphenoxyacetic acid 3, 2-(2,4-diclilorophenoxy) propanoic acid 4, 2-(4-cliloro-2-methylphenoxy) propanoic acid 5, 2,4,5-trichlorophenoxyacetic acid 6, 4-(2,4-dichlorophenoxy) butanoic acid 7, 4-(4-chloro-2-methylphenoxy) butanoic acid 8, 2-(2,4,5-tiichlorophenoxy) propionic acid. Reprinted from Analytica Chimica Acta, 283, J. V. Sancho-Llopis et al., Rapid method for the determination of eight chlorophenoxy acid residues in environmental water samples using off-line solid-phase extraction and on-line selective precolumn switcliing , pp. 287-296, copyright 1993, with permission from Elsevier Science.

J. V. Sancho-Elopis, E. Hernandez-Hernandez, E. A. Hogendoorn and P. van Zoonen, Rapid method for the determination of eight clilor ophenoxy acid residues in envhon-mental water samples using off-line solid-phase excaction and on-line selective precolumn switching . Anal. Chim. Acta 283 287-296(1993). 

Baker and Smith have devised an improved rapid method which they find works well with oils containing 20 per cent, and over. Eucalyptus oils which give a compound that cannot be satisfactorily pressed by the British Pharmacopoeia method may be readily determined in this way and the decomposition of the cineol phosphate by long pressing (particularly in hot countries) is prevented. 

Method development remains the most challenging aspect of chiral chromatographic analysis, and the need for rapid method development is particularly acute in the pharmaceutical industry. To complicate matters, even structurally similar compounds may not be resolved under the same chromatographic conditions, or even on the same CSP. Rapid column equilibration in SFC speeds the column screening process, and automated systems accommodating multiple CSPs and modifiers now permit unattended method optimization in SFC [36]. Because more compounds are likely to be resolved with a single set of parameters in SFC than in LC, the analyst stands a greater chance of success on the first try in SFC [37]. The increased resolution obtained in SFC may also reduce the number of columns that must be evaluated to achieve the desired separation. 

Requirements for cans for beer and soft drinks differ from those for food cans in that (a) only low tin and iron contents can be tolerated in the product and (t>) the anticipated shelf-lives are much shorter. Specialised lacquering techniques including striping the seams are used to give complete cover to the metal. For soft drinks it is sometimes possible to select colouring matters and acids least likely to give rise to corrosion troubles, and rapid methods of testing formulations have been devised . Steel quality is also controlled by special tests. 

A relationship was also established between the oxide-reduction time and time of exposure, and the results for a mild steel and a lCu-3Ni weathering steel were similar to those obtained by mass loss. The authors give various expressions that relate oxide-reduction time (min) with corrosion rate (mm/y), and claim that a short exposure to a laboratory SO2 atmosphere followed by determining the E vs. time and oxide-reduction time provides a rapid method of evaluating weathering steels. 

Reactivation Ratio EPR Test (Fig. 19.20c) This is a simpler and more rapid method than the single or double loop tests, and depends on the fact that the value of determined during the anodic scan of a double loop test (which produces general dissolution without intergranular attack on sensitised material) is essentially the same for all AlSl Type 304 and 304L steels. 

A successful program of quality control also involves maintenance of sanitary conditions and production of products free from adulteration, contamination, and filth. Methods given by the Association of Official Agricultural Chemists (1) should be applied to the finished product to ensure against seizure and prosecution by federal and state food and drug authorities. In many instances such methods of analysis are not adaptable to production-line control and less accurate but more rapid methods must be substituted. With such procedures, more severe tolerances must be used to provide a sufficient margin of safety. 

Miscellaneous Determinations. Several other problems are deserving of brief mention. The citrus industry, for example, would welcome an improved and more rapid method for determining volatile oil in citrus products. The tomato canning industry could profit by more rapid and accurate methods for determining tomato solids, and also by a method that would predict the increase in viscosity which takes place during concentration. 

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