Routine orders

This method is suitable for processing routine orders however, where there are nonstandard conditions a more variable process needs to be developed. Providing you define the approach you intend to take in your procedures, you should be able to demonstrate that your methods provide an adequate degree of control. 

Routine orders This is an ongoing order given for a specific number of doses or number of days. 

Already, oncologists routinely order PET scans to stage a patient s cancer or to look for new cancers. Breast tumors, for example, consume more FDG than the surrounding tissue. So the tumors trap the FDG and appear as hot spots. These whole-body scans move from the mid-thigh to about the base of the skull. It would take little extra time or expense to continue scanning to the top of the head and image the brain and would require no extra exposure to radiation from the FDG. 

Using scans to monitor potential risks is not a new idea. Oncologists, for instance, routinely order a different type (called MUGA, multiple gated acquisition scans) to measure heart function in patients who are on doxorubicin-type compounds and/or the targeted therapy trastuzumab (Herceptin). 

The choice and importance of different attributes varies in relation to the buying situation. Delivery reliability, price, and supplier reputation are important for routine-order products, but for procedural-problem prod-... 

UoK, Porton Archive, A204, Porton Experimental History WWI to WWII. Station (routine) orders (SROs), normally displayed on mess notice boards, governed servicemen s daily lives. 

If Langmuir adsorption occurs, then a plot of 9 versus p for a particular isothenn will display the fonn of equation (Al.7.3). Measurements of isothenns are routinely employed in this manner in order to detennine adsorption kinetics. 

The chief disadvantage of the simple vacuum distillation set up shown in Fig. 11,19, 1 is that, if more than one fraction is to be collected, the whole process must be stopped in order to change the receiver B. It is of value, however, for the distillation of solids of low melting point the distillate can easily be removed from the receiver by melting and pouring out. For routine work, involving the collection of several fractious under reduced pressure, the most convenient receiver is the so-called Perkin triangle the complete apparatus for vacuum distillation is depicted in F g. 11,20, 1. The Claisen fla.sk A is fitted to a. short water... 

It is frequently advisable in the routine examination of an ester, and before any derivatives are considered, to determine the saponification equivalent of the ester. In order to ensure that complete hydrolysis takes place in a comparatively short time, the quantitative saponi fication is conducted with a standardised alcoholic solution of caustic alkali—preferably potassium hydroxide since the potassium salts of organic acids are usuaUy more soluble than the sodium salts. A knowledge of the b.p. and the saponification equivalent of the unknown ester would provide the basis for a fairly accurate approximation of the size of the ester molecule. It must, however, be borne in mind that certain structures may effect the values of the equivalent thus aliphatic halo genated esters may consume alkali because of hydrolysis of part of the halogen during the determination, nitro esters may be reduced by the alkaline hydrolysis medium, etc. 

Chapter 10 represented a wave function as a linear combination of Gaussian basis functions. Today, there are so many basis sets available that many researchers will never need to modify a basis set. However, there are occasionally times when it is desirable to extend an existing basis set in order to obtain more accurate results. The savvy researcher also needs to be able to understand the older literature, in which basis sets were customized routinely. 

Organic molecule calculations can be done routinely to good accuracy on workstation-class hardware. It is advisable to examine tabulations of results in order to choose a method with acceptable accuracy and computational time for the property of interest. The trend toward having microcomputer versions of computational chemistry codes is making calculations on small organic molecules even more readily accessible. 

However unlike H which is the most abundant of the hydrogen isotopes (99 985%) only 1 1% of the carbon atoms m a sample are Moreover the intensity of the signal produced by nuclei is far weaker than the signal produced by the same number of H nuclei In order for NMR to be a useful technique in structure deter mination a vast increase in the signal to noise ratio is required Pulsed FT NMR pro vides for this and its development was the critical breakthrough that led to NMR becoming the routine tool that it is today... 

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. 

The source requited for aes is an electron gun similar to that described above for electron microscopy. The most common electron source is thermionic in nature with a W filament which is heated to cause electrons to overcome its work function. The electron flux in these sources is generally proportional to the square of the temperature. Thermionic electron guns are routinely used, because they ate robust and tehable. An alternative choice of electron gun is the field emission source which uses a large electric field to overcome the work function barrier. Field emission sources ate typically of higher brightness than the thermionic sources, because the electron emission is concentrated to the small area of the field emission tip. Focusing in both of these sources is done by electrostatic lenses. Today s thermionic sources typically produce spot sizes on the order of 0.2—0.5 p.m with beam currents of 10 A at 10 keV. If field emission sources ate used, spot sizes down to ca 10—50 nm can be achieved. 

Most aroma chemicals are relatively high boiling (80—160°C at 0.4 kPa = 3 mm Hg) Hquids and therefore are subject to purification by vacuum distillation. Because small amounts of decomposition may lead to unacceptable odor contamination, thermal stabiUty of products and by-products is an issue. Important advances have been made in distillation techniques and equipment to allow routine production of 5000 kg or larger batches of various products. In order to make optimal use of equipment and to standardize conditions for distillations and reactions, computer control has been instituted. This is particulady well suited to the multipurpose batch operations encountered in most aroma chemical plants. In some instances, on-line analytical capabihty is being developed to work in conjunction with computer controls. 

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