Limitations of the method

The primary limitation of this technique is the need to suspend the powder in an electrolyte. For powders insoluble in water a 0.9% saline solution is often used and dispersion effected using ultrasonics. The manufacturers also provide a list of electrolytes for use with water-soluble materials but these can cause cleaning difficulties. 

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Much work remains to be done in the development of this approach to explore the advantages and limitations of the method. The method will be extended to force fields that include torsional terms large systems such as biological macromolecules will also be treated. 

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. 

An important benefit of QSAR methods is that no enzyme stmcture is required. However, a series of stmcturaHy related inhibitors of known stmcture and known inhibitory activity is required. The limitations of the method involve the difficulties in describing something as compHcated as a stmcture-function relationship in a single mathematical expression. 

Matrix-assisted laser desorption/ionization (MALDI) is widely used for the detection of organic molecules. One of the limitations of the method is a strong matrix background in low-mass (up to 500-700 Da) range. In present work an alternative approach based on the application of rough matrix-less surfaces and known as surface-assisted laser desoi ption/ionization (SALDI), has been applied. 

Volkov and Sushko [335] described a technique that is based on the use of nets. This method provides direct absorption spectra, but is very complex to perform The net must be placed in a chamber that ensures a pure inert atmosphere so as to avoid hydrolysis of the melt, and the temperature and geometry of the net must be kept very stable. Other major limitations of the method are the requirements that the surface tension of the melt be such that its position on the net is ensured, and that the vapor pressure of the material in molten state be as low as possible... 

Determination of cadmium as quinaldate Discussion. Quinaldic acid or its sodium salt precipitates cadmium quantitatively from acetic (ethanoic) acid or neutral solutions. The precipitate is collected on a sintered-glass crucible, and dried at 125 °C. A determination may be completed in about 90 minutes. For the limitations of the method, see Section 11.11(G). 

The results in Table VI are of considerable interest also for atoms with more than two electrons, since they show the possibilities and limitations of the method of superposition of configurations/ when the latter are built up from one-electron functions... 

The most fundamental limitation of the method is implicit in Equation 1-9. As all atoms absorb x-rays, the method cannot be specific it cannot ordinarily identify unknown elements in a sample, nor can it ordinarily give reliable analytical results on a sample containing unknown elements. On the other hand, it can usually show whether or not such a sample has an assumed ultimate composition.7... 

Some limitations of the method arise due to side reactions involving the nitroxide. However, such problems can usually be avoided by the correct choice of nitroxide and reaction conditions. Nitroxides, while stable in the presence of most monomers, may act as oxidants or rcductants under suitable reaction conditions.516 The induced decomposition of certain initiators (e.g. diacyl peroxides) can be a problem (Scheme 3.94).166 177 There is some evidence that nitroxides may disproportionate with alkoxy radicals bearing a-hydrogens,123 Side reactions with thiols have also been identified.4 18... 

In the past few years this pulsing technique has been used by several groups, utilizing both magnetic deflection (16, 31, 37) and time-of-flight (12, 13) instruments, to study ion-molecule reactions at thermal energies. Here we review the results obtained and discuss the applications and limitations of the method, based on our observations and experiences over the past three years. 

Regarding the series of hetero aromatic pentacyclic compounds with three heteroatoms, an accelerated synthesis of 3,5-disubstituted 4-amino-1,2,4-triazoles 66 under microwave irradiation has been reported by thermic rearrangement of dihydro-1,2,4,5 tetrazine 65 (Scheme 22). This product was obtained by reaction of aromatic nitriles with hydrazine under microwave irradiation [53]. The main limitation of the method is that exclusively symmetrically 3,5-disubstituted (aromatic) triazoles can be obtained. 

Generally, the closure problem reflects the idea of a spatially periodic porous media, whereby the entire structure can be described by small portions (averaging volumes) with well-defined geometry. Two limitations of the method are therefore related to how well the overall media can be represented by spatially periodic subunits and the degree of difficulty in solving the closure problem. Not all media can be described as spatially periodic [6,341 ]. In addition, the solution of the closure problem in a complex domain may not be any easier than solving the original set of partial differential equations for the entire system. 

The first cross metathesis to form a tetra-substituted olefin was achieved recently [146]. Howell and co-workers used lactams as substrates for CM with mono- and di-substituted olefins. The authors suggest that the limitations of the method are primarily due to steric reasons. Varying the electron density of the lactam showed no great influence on the reactivity while steric influences like a-branched allylic crosspartners or a methyl-group in the C4-position of the lactam both led to no reaction (Scheme 3.13). 

Pharmacopoeial standards and substances are established and distributed by pharmacopoeial authorities following the general principles of this Guide. It should be noted, however, that a different approach is used by the pharmacopoeial authorities to give the user the information provided by certificates of analysis and expiration dates. Also, the uncertainty of their assigned values is not stated since it is negligible in relation to the defined limits of the method-specific assays of the pharmacopoeias for which they are used. ... 

SEC has sometimes been used with off-line IR spectroscopy for the detection of polymer additives, such as dioctylphthalate, as well as on-line [39]. Dissolutions of PVC/DEHP and of PC/pentaerythritoltetrastearate (release agent) were analysed by SEC-FTIR using the thermospray/moving belt/DRIFT interface [40]. The detection limits of the method were in the 100 ng range, depending on the IR sensitivity and volatility of the solutes. This is not extremely sensitive. 

Care must be exercised in applying the UNIFAC method. The specific limitations of the method are ... 

It is important for the designer to understand the limitations of the methods used in chemical process design. The best way to understand the limitations is to understand the derivations of the equations used and the assumptions on which the equations are based. Where practical, the derivation of the design equations has been included in the text. 

Faradaic rectification polarographic studies have been carried out for a mixture containing several metal ions together and also for individual inorganic depolarizers so as to explore the applicability and limitations of the method and to determine kinetic parameters for some of them. For comparison, some of the dc and ac polarograms have also been recorded simultaneously. In the following, the details of the experimental technique used will be described and the potentiality of the technique in qualitative and quantitative analysis will be examined. The applicability of the method in the... 

Libraries of /3-turn mimetics have been prepared by solid-phase syntheses. The synthesis of the chiral saturated pyrazino[l,2- ]pyrazine 243 starts from Merrifield resin-bound a-iV-BOC-/3-./V-Fmoc-L-diaminopropionic acid as the central framework. The variable substituents are introduced during the synthesis (Scheme 43) <20000L2615>. The scope and limitations of the method are described <2002JC0584>. 

The limitations of the method come from the stability of the complexes under sol gel conditions however, even biocatalysts can be suitable for entrapment in sol-gel materials.87... 

Ruzic [278 ] considered the theoretical aspects of the direct titration of copper in seawaters and the information this technique provides regarding copper speciation. The method is based on a graph of the ratio between the free and bound metal concentration versus the free metal concentration. The application of this method, which is based on a 1 1 complex formation model, is discussed with respect to trace metal speciation in natural waters. Procedures for interpretation of experimental results are proposed for those cases in which two types of complexes with different conditional stability constants are formed, or om which the metal is adsorbed on colloidal particles. The advantages of the method in comparison with earlier methods are presented theoretically and illustrated with some experiments on copper (II) in seawater. The limitations of the method are also discussed. 

Berman et al. [735] have shown that if a seawater sample is subjected to 20-fold preconcentration by one of the above techniques, then reliable analysis can be performed by ICP-AES (i.e., concentration of the element in seawater is more than five times the detection limit of the method) for iron, manganese, zinc, copper, and nickel. Lead, cobalt, cadmium, chromium, and arsenic are below the detection limit and cannot be determined reliably by ICP-AES. These latter elements would need at least a hundredfold preconcentration before they could be reliably determined. 

Bhat et al. [199] used complexation with the bis(ethylenediamine) copper (II) cation as the basis of a method for estimating anionic surfactants in fresh estuarine and seawater samples. The complex is extracted into chloroform, and copper is measured spectrophotometrically in the extract using l,2(pyridyl azo)-2-naphthol. Using the same extraction system these workers were able to improve the detection limit of the method to 5 pg/1 (as linear alkyl sulfonic acid) in fresh estuarine and seawater samples. 

The approximate detection limits of the method range from 1 fg CCI4 to 500 fg CH2CC12. 

Pongratz and Hunmann [19], using differential pulse anodic scanning voltammetry, found low levels of methyl cadmium compounds in the Atlantic Ocean. Levels in the South Atlantic were approximately 700 pg/1, and those in the North Atlantic were below the detection limit of the method, i.e., below 470 pg/1. It is believed that these compounds were formed as a result of biomethylation of inorganic cadmium. 

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