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Aquatic suspensions

At the surface of the earth, there exist countless examples of suspensions, including the suspended mineral and humic matter particles carried by streams and rivers, and are found in lakes and oceans [4, 5]. The sediments formed from these suspensions, once the voids are filled in and cemented in place by other [Pg.307]

Emulsions, loams, Suspensions, and Aerosols Microscience and Applications, [Pg.307]

Foams Free gas bubbles in oceans, lakes and rivers G/W [Pg.308]

The total particulate matter in the aqueous environment occurs in both suspended and dissolved forms, and is usually represented by the term total solids (TS) given by [Pg.308]

Particle type Diameter (pm) Sedimentation velocity (cm s ) Time to sediment 4 km [Pg.309]


The size distribution of atmospheric aerosols and of aquatic suspensions is often found to follow a power law of the form... [Pg.828]

The extent of surface oxidation, type, and relative ratio of surface oxide functional groups on CNTs, and solution chemistry of the aqueous environment will dictate the sorption properties of CNTs and whether the CNT agglomerates form stable suspensions or settle out of solution. The tendency of CNTs to setfle in an aquatic suspension as a function of the extent of oxidation is shown in Figure 21.9 (25). The CNTs were vortexed in a salt solution and allowed to settle for two hours. After two hours, the... [Pg.696]

Layer silicates are also eminently suitable for the preparation of particles with a diameter of a few nanometers on the surface and in the interlamellar space of clays in aquatic suspensions. Particle growth in the interlamellar space is sterically hindered. [Pg.88]

Transport in solution or aqueous suspension is the major mechanism for metal movement from the land to the oceans and ultimately to burial in ocean sediments. In solution, the hydrated metal ion and inorganic and organic complexes can all account for major portions of the total metal load. Relatively pure metal ores exist in many places, and metals from these ores may enter an aquatic system as a result of weathering. For most metals a more common sequence is for a small amount of the ore to dissolve, for the metal ions to adsorb onto other particulate matter suspended in flowing water, and for the metal to be carried as part of the particulate load of a stream in this fashion. The very insoluble oxides of Fe, Si, and A1 (including clays), and particulate organic matter, are the most important solid adsorbents on which metals are "carried."... [Pg.415]

Seeds of lettuce and other species have frequently been used to bioassay for the allelopathic activity of plant exudates (17.18.19). As with the use of cell suspensions, there are certain advantages and disadvantages to this methodology. The experimental simplicity, small amounts of material required and short time frame are certainly attractive qualities. However, species used in such bioassays quite often do not represent the actual target species under consideration. This is especially true when terrestrial crop species are substituted for weeds of aquatic systems. Nevertheless, information obtained from such experiments are often valuable when used in conjunction with results of other assays. [Pg.410]

Many of the PCBs found in the aquatic environment (e.g., in lakes and in the Arctic and Antarctic) have migrated via atmospheric dispersion of vapors [404-410]. Vaporization of PCBs from soil decreases as the amount of humic material in the solid phase increases due to mainly partitioning processes [381-390]. Griffin and Chian [363] note that vaporization of PCBs from suspensions of solids or humic acids is reduced by the presence of these materials. [Pg.282]

Paul FA, Qark FE (1989) Soil microbiology and biochemistry. Academic Press, New York Pecher K, HaderUne SB, Schwarzenbach RP (2002) Reduction of polyhalogenated methanes by surface— b Fe(ll) in aqueous suspensions of iron oxides. Environ Sci Technol 36 1734-1741 Penrose WR, Metta DN, Hyfko JM, Rinkel LA (1987) The reduction of plutonium (V) by aquatic sediments. J Environ Radioact 5 169-184... [Pg.406]

It was clearly shown by EPR measurements that irradiation of aqueous suspensions of Ti02 and surfacted or encapsulated fullerene derivatives leads to the formation of fullerene radical anions by electron transfer from excited Ti02. The reduction of the embedded derivative compared to the surfacted one is more efficient [183], However, in comparison to organic solvents, the reduction yield of the fullerenes radical anions in aqeous media is lower. This may be explained by the influence of the aquatic environment and the stability of the radical anions formed [183,184], Nevertheless, electron transfer still occurs from the donor to the fullerenes triplet-excited state [182,185,186],... [Pg.674]

Mansour, M. (1996). Abiotic degradation of pesticides and other organic chemicals in aquatic systems. Pestic. Outlook, 7 9-10. Mansour, M., A. Mamouni, and P. Meallier (1988). Factors determining the behavior and transformation of selected pesticides in water, soil suspension and soils. In Proceedings of Methodological Aspects of the Study of Pesticide Behaviour in Soil. Versailles, France, INRA, June 16-17, pp. 87-100. [Pg.351]

Sandbacka, M., Part, P. and Isomaa, B. (1999) Gill epithelial cells as tools for toxicity screening -comparison between primary cultures, cells in suspension and epithelia on filters, Aquatic Toxicology... [Pg.61]

Intermediates and Reaction Pathway. Identification of Inter mediates. The derivatization technique and GC-MS analysis were success fully used to detect organic pollutants in the aquatic environment (26, 27) This same technique was chosen to identify the partial oxidation products o 4-chIorophenol in Ti02 aqueous suspensions. Figure 5 and Table II show th< mass spectra of the derivadzed reaction products of 4-chlorophenol. Fou derivatized intermediate peaks [A, B, C, and D, with retention times (RTs at 10.32, 12.50, 13.72, and 14.11 min, respectively] were observed. Peak A i the acetylated parent compound, 4-chlorophenol. Peaks B, C, and D are ace tylated intermediate products. The identification of peaks B, C, and D wa based on the following observations ... [Pg.300]

Figure 12.7 Summary plot of experimentally derived stability ratios, of hematite suspensions as a function of added electrolyte concentration at about pH 6.5. Hematite concentration is about 20 mg/L. HA and FA are Suwannee River humic and fuivic acid, for which total concentrations are expressed as equivalents of carboxylate group (-COOH). From Aquatic Sciences 52(1) 32-55, L. Liang and J. J. Morgan, Chemical aspects of iron oxide coagulation in water Laboratory studies and implications for natural systems, Copyright 1990 by Birkhauser Verlag, Basel, Switzerland. Used by permission. Figure 12.7 Summary plot of experimentally derived stability ratios, of hematite suspensions as a function of added electrolyte concentration at about pH 6.5. Hematite concentration is about 20 mg/L. HA and FA are Suwannee River humic and fuivic acid, for which total concentrations are expressed as equivalents of carboxylate group (-COOH). From Aquatic Sciences 52(1) 32-55, L. Liang and J. J. Morgan, Chemical aspects of iron oxide coagulation in water Laboratory studies and implications for natural systems, Copyright 1990 by Birkhauser Verlag, Basel, Switzerland. Used by permission.

See other pages where Aquatic suspensions is mentioned: [Pg.307]    [Pg.307]    [Pg.54]    [Pg.409]    [Pg.204]    [Pg.264]    [Pg.25]    [Pg.132]    [Pg.639]    [Pg.361]    [Pg.2]    [Pg.438]    [Pg.14]    [Pg.359]    [Pg.132]    [Pg.152]    [Pg.286]    [Pg.332]    [Pg.106]    [Pg.373]    [Pg.105]    [Pg.15]    [Pg.636]    [Pg.835]    [Pg.847]    [Pg.496]    [Pg.4680]    [Pg.84]    [Pg.87]    [Pg.16]    [Pg.257]    [Pg.469]    [Pg.470]    [Pg.93]    [Pg.146]   
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