Historical dispersal

Historically dispersions of small magnetic particles having a superparamagnetic nature were used for the observation of magnetic domains. Recently nanoparticles have been intensively studied because of their unique physical properties, which cannot be achieved by bulk materials. 

Historically, dispersions of small magnetic particles with a superparamagnetic nature were used for observing magnetic domains. When a concentrated suspension of magnetic particles is placed in the gradient of a magnetic field. 

The array system is discussed in Chapter 29. With array detection, resolution of m/z values depends both on the analyzer and the collector. Historically, the method for recording ions dispersed in space was to use a photographic plate, which was placed in the focal plane such that all ions struck the photographic plate simultaneously but at different positions along the plate, depending on m/z value. This method of detection is now rarely used because of the inconvenience of having to develop a photographic plate. 

There is potential confusion in the use of the word array in mass spectrometry. Historically, array has been used to describe an assemblage of small single-point ion detectors (elements), each of which acts as a separate ion current generator. Thus, arrival of ions in one of the array elements generates an ion current specifically from that element. An ion of any given m/z value is collected by one of the elements of the array. An ion of different m/z value is collected by another element. Ions of different m/z value are dispersed in space over the face of the array, and the ions are detected by m/z value at different elements (Figure 30.4). 

To differentiate tteir functions and modes of operation, the array collector of spatially dispersed m/z values is still called an array collector for historical reasons, but the other multipoint detector of a temporally dispersed range of m/z values is called a microchannel plate (typically used in time-of-flight instruments). 

The phenomena we discuss, phase separation and osmotic pressure, are developed with particular attention to their applications in polymer characterization. Phase separation can be used to fractionate poly disperse polymer specimens into samples in which the molecular weight distribution is more narrow. Osmostic pressure experiments can be used to provide absolute values for the number average molecular weight of a polymer. Alternative methods for both fractionation and molecular weight determination exist, but the methods discussed in this chapter occupy a place of prominence among the alternatives, both historically and in contemporary practice. 

The use of alkaU metals for anionic polymerization of diene monomers is primarily of historical interest. A patent disclosure issued in 1911 (16) detailed the use of metallic sodium to polymerize isoprene and other dienes. Independentiy and simultaneously, the use of sodium metal to polymerize butadiene, isoprene, and 2,3-dimethyl-l,3-butadiene was described (17). Interest in alkaU metal-initiated polymerization of 1,3-dienes culminated in the discovery (18) at Firestone Tire and Rubber Co. that polymerization of neat isoprene with lithium dispersion produced high i7j -l,4-polyisoprene, similar in stmcture and properties to Hevea natural mbber (see ELASTOLffiRS,SYNTHETic-POLYisoPRENE Rubber, natural). 

Azo Dyes. The Colourindex classifications of dyes depend more on their historical eady use than on their stmctures, eg. Oil Orange is named Solvent Yellow 14, and a yellow for synthetic fibers is Disperse Yellow 23. 

Historically the most common gas disperser for cross-flow plates has been the bubble cap. This device has a built-in seal which prevents liquid drainage at low gas-flow rates. Typical bubble caps are shown in Fig. 14-20. Gas flows up through a center riser, reverses flow under the cap, passes downward through the annulus between riser and cap, and finally passes into the liquid through a series of openings, or slots, in the lower side of the cap. 

The theory that results from the investigation of the dynamics of solute distribution between the two phases of a chromatographic system and which allows the different dispersion processes to be qualitatively and quantitatively specified has been designated the Rate Theory. However, historically, the Rate Theory was never developed as such, but evolved over more than a decade from the work of a number of physical chemists and chemical engineers, such as those mentioned in chapter 1. 

Column dispersity (band spreading) causes the measured molecular weight distribution to be broader than the true molecular weight distribution (Fig. 3.5). Because Zorbax PSM columns exhibit very low band-spreading characteristics, these columns have historically provided better molecular weight distribution accuracy than many gel-type columns. 

Cause-consequence analysis serx es to characterize tlie physical effects resulting from a specific incident and the impact of these physical effects on people, the environment, and property. Some consequence models or equations used to estimate tlie potential for damage or injury are as follows Source Models, Dispersion Models, Fire Explosion Models, and Effect Models. Likelihood estimation (frequency estimation), cliaractcrizcs the probability of occurrence for each potential incident considered in tlie analysis. The major tools used for likelihood estimation are as follows Historical Data, Failure sequence modeling techniques, and Expert Judgment. 

Once the model was complete, it was adjusted to a steady state condition and tested using historic carbon isotope data from the atmosphere, oceans and polar ice. Several important parameters were calculated and chosen at this stage. Sensitivity analysis indicated that results dispersal of the missing carbon - were significantly influenced by the size of the vegetation carbon pool, its assimilation rate, the concentration of preindustrial atmospheric carbon used, and the CO2 fertilization factor. The model was also sensitive to several factors related to fluxes between ocean reservoirs. 

With the establishment of clear-cut flavone races, the next obvious question was how the pattern became established. One possibility discussed by Mastenbroek (1983) involved selection for flavone profiles in response to some environmental factor or factors, climatological or edaphic being the most obvious ones. Alternatively, the present-day distribution pattern may be the result of historical factors (1) migration involving long- or intermediate-distance dispersal (2) range extension... 

Herein we briefly mention historical aspects on preparation of monometallic or bimetallic nanoparticles as science. In 1857, Faraday prepared dispersion solution of Au colloids by chemical reduction of aqueous solution of Au(III) ions with phosphorous [6]. One hundred and thirty-one years later, in 1988, Thomas confirmed that the colloids were composed of Au nanoparticles with 3-30 nm in particle size by means of electron microscope [7]. In 1941, Rampino and Nord prepared colloidal dispersion of Pd by reduction with hydrogen, protected the colloids by addition of synthetic pol5mer like polyvinylalcohol, applied to the catalysts for the first time [8-10]. In 1951, Turkevich et al. [11] reported an important paper on preparation method of Au nanoparticles. They prepared aqueous dispersions of Au nanoparticles by reducing Au(III) with phosphorous or carbon monoxide (CO), and characterized the nanoparticles by electron microscopy. They also prepared Au nanoparticles with quite narrow... 

The nitro group is commonly encountered as a substituent in dyes and pigments of most chemical classes, but it acts as the essential chromo-phore in only a few dyes. Nitro dyes are a small group of dyes of some importance as disperse dyes for polyester and as semi-permanent hair dyes. Picric acid, 139, was historically the first nitro dye, although it was... 

As with prisms, there are other devices that have been historically used for dispersing or filtering electromagnetic radiation. These include interference filters and absorption filters. Both of these are used for monochromatic instruments or experiments and find little use compared to more versatile instruments. The interested reader is referred to earlier versions of instrumental analysis texts. 

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