Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Pore water chemistry limitations

Electrokinetic remediation is limited by the type of contaminant, heterogeneities or anomalies in the soil, extreme pHs, pore water chemistry, lack of pore water, contaminant and noncontaminant ion concentrations, metals precipitation, and reduction-oxidation changes induced by the process electrode reactions. It may be difficult to estimate the time that will be required to remediate a site using this technology. Laboratory treatability testing may provide a false indication of the applicability of electrokinetic remediation at a specific site. Further research is required to determine the technology s limitations and ramifications. [Pg.531]

The presence of iron minerals and their respective reactivity towards sulfide is of greatest importance for the pore water chemistry and the limitation for pyrite formation. In case of reactive iron rich sediments dissolved iron may build-up in pore water and dissolved sulfide is hardly present although sulfate reduction occurs. In contrast, in sediments characterized by a low content of reactive iron dissolved sulfide can build-up instead of dissolved iron (Canfield 1989). The degree of pyritisation (DOP) was originally defined by Berner (1970) and was later modified by Leventhal and Taylor (1990) and Raiswell et al. (1994). DOP is now defined as ... [Pg.253]

The theoretical prediction of whether a particular pollutant will be soluble (and hence potentially mobile) or insoluble (and hence potentially immobile) using pore-water chemistry data is more problematical. This limitation arises because it is impossible to derive reliable estimates of in situ concentrations for several key constituents using the techniques described. In particular, reliable data for in situ pH and redox conditions Eh) cannot be acquired. This is particularly true when pore-waters cannot be extracted directly and compositions must instead be estimated from leachate data. Although there are limitations in the use of pore-water data to... [Pg.270]

Most of our understanding of the marine chemistry of trace metals rests on research done since 1970. Prior to this, the accuracy of concentration measurements was limited by lack of instrumental sensitivity and contamination problems. The latter is a consequence of the ubiquitous presence of metal in the hulls of research vessels, paint, hydrowires, sampling bottles, and laboratories. To surmount these problems, ultra-clean sampling and analysis techniques have been developed. New methods such as anodic stripping voltammetry are providing a means by which concentration measurements can be made directly in seawater and pore waters. Most other methods require the laborious isolation of the trace metals from the sample prior to analysis to eliminate interferences caused by the highly concentrated major ions. [Pg.259]

Although zeolites are stable in water, their narrow pore openings considerably limit their utilization in carbohydrate chemistry. In most cases, only the external surface is accessible to reactants. For these reasons, many investigations have focused on mesoporous silica-supported sulfonic sites (Fig. 1). The presence of uniform channel with large pore openings (2-9 nm) offer notable advantages over zeolites. [Pg.68]

Because of their low permeability, flowing groundwaters cannot generally be obtained from clays and mudrocks. Although fracture flows can frequently be induced from crystalline formations, the frequency of features such as open fractures that conduct water flow is normally limited. To evaluate the chemistry within geological and engineered barriers it is necessary, therefore, to characterize matrix pore-waters obtained using speciaUzed extraction techniques. [Pg.265]

Capillaries in the Brain (the Blood-Brain Barrier). Capillaries in the brain are less permeable than capillaries in other tissues. This limited permeability, which is frequently called the blood-brain barrier, is essential for brain function. Reduced permeation provides a buffer that maintains a constant brain extracellular environment, even at times when blood chemistry is changing. The basis for this lower permeability is the relative paucity of pores in the brain endothelium. Therefore, molecules that move from blood to brain must diffuse through the endothelial cell membranes. As expected from this observation, the permeability of brain capillaries depends on the size and lipid solubility of the solute. In general, molecules that are larger than several hundred in molecular weight do not permeate into the brain. Empirical relationships between cerebrovascular permeability and the oil / water partition coefficient have been developed [26] (see Figure 5.27) ... [Pg.147]

Many studies have aimed to prepare mesoporous solids with active titanium, either by direct synthesis or by post-synthetic modifications. Although some of the advantages of crystalline framework solids are lost, the larger pore size increases markedly the size limit of molecules that can be converted by this catalytic chemistry, and active and selective catalysts have been prepared. In addition, such solids can be used with organic peroxides (such as tert-butylhy-droperoxide) that do not produce water as an inhibiting by-product. [Pg.375]

Another consequence of the fixed pores and the rigid structure (high DVB levels) is that macroporous resins have limited swelling. Thus a wide range of solvents commonly used in organic synthesis can be used in solid-phase macroporous resin assisted chemistry (even water), without modification of the reaction conditions as required for the use of gel-type resins. Moreover, the rigid structure makes these supports very resistant to mechanical agitation and easy to handle (macroporous resins do not stick like gel type resins). [Pg.6409]

In the past few years, great progress has been made for the applications of MOFs in analytical chemistry. Although some kinds of MOFs that are water instable have limited applications in analytical chemistry, MOFs that have good thermostability and water stability (such as ZIF and MIL MOFs) can be available in almost all the important aspects of modern analytical chemistry. With well-defined pore structures, MOFs have great potential in adsorption and adsorption-based separation. Also, MOFs have been engineered to specific forms such as columns, fibers, and films to meet various analytical challenges and... [Pg.454]


See other pages where Pore water chemistry limitations is mentioned: [Pg.118]    [Pg.2]    [Pg.501]    [Pg.381]    [Pg.167]    [Pg.4720]    [Pg.5137]    [Pg.150]    [Pg.356]    [Pg.338]    [Pg.569]    [Pg.179]    [Pg.602]    [Pg.124]    [Pg.98]    [Pg.587]    [Pg.315]    [Pg.348]    [Pg.517]    [Pg.234]    [Pg.427]    [Pg.273]    [Pg.490]    [Pg.285]    [Pg.418]    [Pg.143]    [Pg.43]   
See also in sourсe #XX -- [ Pg.382 , Pg.383 ]




SEARCH



Pore limitations

Pore water chemistry

Pore waters

Water chemistry

Water limitation

© 2024 chempedia.info