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Water environment

P. A. VeUa, J. Munder, and B. Veronda, "Chemical Oxidation A Tool for Toxicity Reduction and Bio-Enhancement," presented at the 65th Water Environment Federation Conference and Exposition, New Orleans, La., Sept. 1992. [Pg.532]

R. J. Pope and R. A. Weber, Water Environment Federation Proceedings of the 66th Annual Conference and Exposition, 1993, pp. 447—456. [Pg.532]

Biodegradation results from the pH drop such a detergent polymer experiences as it leaves the alkaline laundry environment (pH ca 10) and enters the sewage or ground water environment (pH close to neutral) the polymer (now a polyacid rather than a salt) is unstable and hydrolyzes to monomer which rapidly biodegrades. The chemistry has been reported ia many patents (186) and several pubHcations (187,188). [Pg.482]

Water Environment Eederation (formerly Water Pollution Control Eederation), Hazardous Waste Treatment Processes, Manual of Practice ED-18, prepared by Task Eorce on Hazardous Waste Treatment, Alexandria, Va., 1990. [Pg.173]

Water Environment Pederation, Water Environ. Technol 6(8), 26 (1994). [Pg.174]

American Water Works Association, American PubHc Health Association, and Water Environment Eoundation, Standard Methodsfor the Examination of Water and Wastewater, 18th ed., American PubHc Health Assc., Washington, D.C., 1992. [Pg.205]

Fig. 1. Natural water environments. Water links essential cycles of the atmosphere with those of the sediments. Fig. 1. Natural water environments. Water links essential cycles of the atmosphere with those of the sediments.
John S. Jeris, Sc.D., P.E., Professor of Environmental Engineering, Manliattan College Environmental Consultant Member, American Water Works Association, Water Environment Federation Section Director (Section 2.5, Waste Management)... [Pg.12]

Irwin J Ku9elman/ Sc D / Professor of Civil Engineering, Lehigh University Member, Amencan Society of Civil Engineering, Water Environment Federation. (Wa.stewater Management)... [Pg.2151]

Three types of methods for phosphate analyses have been studied with the aims of monitoring the distribution and circulation of orthophosphate and observing the chemical forms of phosphoms compounds occurring in the natural water environment. [Pg.166]

The three major forms of concentration cell corrosion are crevice corrosion, tuberculation, and underdeposit attack. Each form of corrosion is common in cooling systems. Many corrosion-related problems in the cooling water environment are caused by these three forms of wastage. The next three chapters—Chap. 2, Crevice Corrosion, Chap. 3, Tuberculation, and Chap. 4, Underdeposit Corrosion — will discuss cooling water system corrosion problems. [Pg.9]

The incubation period varies widely depending on such factors as crack morphology, water chemistry, and temperature. However, experience in a wide variety of cooling water environments has shown that many stainless alloys develop noticeable attack within 6 months of first being exposed to water. It is rare to see attack initiating many years after equipment commissioning unless service conditions change in the interim. [Pg.20]

Substituting one alloy for another may be the only viable solution to a specific corrosion problem. However, caution should be exercised this is especially true in a cooling water environment containing deposits. Concentration cell corrosion is insidious. Corrosion-resistant materials in oxidizing environments such as stainless steels can be severely pitted when surfaces are shielded by deposits. Each deposit is unique, and nature can be perverse. Thus, replacement materials ideally should be tested in the specific service environment before substitution is accepted. [Pg.85]

Certain alloys frequently used in cooling water environments, notably aluminum and zinc, can be attacked vigorously at high pH. These metals are also significantly corroded at low pH and thus are said to be amphoteric. A plot of the corrosion behavior of aluminum as a function of pH when exposed to various compounds is shown in Fig. 8.1. The influence of various ions is often more important than solution pH in determining corrosion on aluminum. [Pg.185]

Metals that depend on a relatively thick protective coating of corrosion product for corrosion resistance are frequently subject to erosion-corrosion. This is due to the poor adherence of these coatings relative to the thin films formed by the classical passive metals, such as stainless steel and titanium. Both stainless steel and titanium are relatively immune to erosion-corrosion in most cooling water environments. [Pg.240]

Because alterations to equipment design can be cumbersome and expensive, a more economical approach may be to change the metallurgy of affected components. Metals used in typical cooling water environments vary in their resistance to erosion-corrosion. Listed in approximate order of increasing resistance to erosion-corrosion, these are copper, brass, aluminum brass, cupronickel, steel, low-chromium steel, stainless steel, and titanium. [Pg.249]

Admiralty brass (70% Cu, 29% Zn, 1% Sn, 0.05% As or Sb) and arsenical aliuninum brass (76% Cu, 22% Zn, 2% Al, 0.05% As) are resistant to dezincification in most cooling water environments. In the recent past, heat exchangers have virtually always been tubed with inhibited grades of brass. Brasses containing 15% or less zinc are almost immune to dezincification. Dezincification is common in uninhibited brasses containing more than 20% zinc. Inhibiting elements include arsenic, antimony, and phosphorus. Without inhibiting elements. [Pg.295]

Strictly speaking, this arrangement is precise only for sea water under controlled laboratory conditions. In other conductive fluids under industrial conditions, the magnitude of the potential, and possibly the position of the metals on the list, could change. In typical cooling water environments, however, the order of the metals as listed for sea water would not be expected to change significantly. [Pg.359]

As Guardians of the Water Environment , the National Rivers Authority (NRA) has statutory duties and powers to protect the aquatic environment from... [Pg.43]

Suffet, 1. H. (ed.), "Fate of Pollutants in the Air and Water Environments, "Part 2," Chemical and Biological Fate of Pollutants in the Environment. Wiley, New York, 1977. [Pg.155]

Gee, C. F., Fatigue properties of Zircaloy-2 in a PWR water environment , Proc. of 1st Int. Conf. on Environmental Degradation of Materials in Nuclear Power Systems- Water Reactors, Myrtle Beach, South Carolina, USA, 22-25 August 1983, NACE, pp. 687-98 (1984)... [Pg.1326]

An interesting example of judicious choice of braze filler is to be found in the selection of silver alloys for the brazing of stainless steels to be subsequently used in a tap-water environment . Although the brazed joint may appear to be quite satisfactory, after a relatively short exposure period failure of the joint occurs by a mechanism which appears to be due to the break-down of the bond between the filler and the base metal. Dezincifica-tion is a prominent feature of the phenomenon and zinc-free braze alloys based on the Ag-Cu system with the addition of nickel and tin have been found to inhibit this form of attack. A similar result is obtained by electroplating 0-007 mm of nickel over the joint area prior to brazing with a more conventional Ag-Cu-Zn-Cd alloy. [Pg.89]

For a hot water environment general guidance can be given for the desirable properties in good enamels. Five factors affecting enamel life are corrosiveness of contact liquor, design, operating conditions, life of sacrificial anode (if any) and the durability of the enamel coat. This implies that... [Pg.898]

Greenberg, A.E., Clesceri, L.S. and Eaton, A.D., Standard Methods for the Examination of Water and Wastewater , 18th edn. American Public Health Association, American Water and Wastewater Association, Water Environment Federation, Washington, DC., 1992. [Pg.49]

OH ion is denoted iff%. The atoms depicted in the figure are considered as our solute system (5) while the rest of the protein-water environment constitutes the solvent (s) for the enzyme reaction. Although the Ca2+ ion does not actually react, it is included in the reacting system for convenience. As before, we describe the diagonal elements of the EVB Hamiltonian associated with the three resonance structures (t/rf,, t/ff) by... [Pg.191]

In order to understand the activity of organotinflV) in water environments (both fresh and seawater), equilibrium and speciahon studies are very important. Moreover, characterizing the structures of hydrolyzed species could be helpful to assess the toxicity mechanism. [Pg.360]

Connell GE (2006) Key operation strategies for chlorine disinfection operating systems. Proceedings of WEFTEC, Water Environment Federation... [Pg.125]


See other pages where Water environment is mentioned: [Pg.234]    [Pg.115]    [Pg.160]    [Pg.212]    [Pg.2210]    [Pg.2213]    [Pg.6]    [Pg.296]    [Pg.21]    [Pg.118]    [Pg.235]    [Pg.330]    [Pg.331]    [Pg.369]    [Pg.1302]    [Pg.1302]    [Pg.1305]    [Pg.1307]    [Pg.1308]    [Pg.1310]    [Pg.111]   
See also in sourсe #XX -- [ Pg.270 ]




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Bulgarian Ministry of Environment and Water

Categorization of water in the environment

Degradation in Sweet Water and Marine Environment

Environment Soil, Air, and Water

Environment shallow water

Environment water pollution

Environment water treatment

Environment, Department water report

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Environment, chemistry salt water

Environment, water absorption

Ground water environment

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Physical conditions, ground water environment

Plutonium in the water environment

Salt water environments

Solute equilibrated with water environment

Water Environment Federation

Water Penetration into Micellar Environment

Water Watery environments

Water and environment

Water aquatic environment

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Water high purity, environment-alloy

Water mixture, environment-alloy

Water primary coordination environment

Water proton environment

Water-soaking environment

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