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Open buffer system

The carbonic acid-bicarbonate buffer system has a of 6.1, yet is still a very effective buffer at pH 7-4 because it is an open buffer system, in which one component, CO2, can equilibrate between blood and air. [Pg.4]

Mount the upper end piece of the filling tube and immediately connect it to the pump, open the column outlet, and start the pump at a flow rate of 10 ml/min (delivering water or any desired buffer system of low ionic strength). Optionally, the column outlet can be additionally connected to a water jet pump, which has to be operated during the first 2 min of packing. The water... [Pg.228]

Epoxidation of olefins with meta-chloroperbenzoic acid, (MCPBA) remains to this day among the most widely used methods for research-scale applications [16], Discovered by Nikolai Prilezahev in 1909 [17], it became popular only decades later, mostly through the works of Daniel Swern in the 1940s [18]. Despite its simplicity, and not unlike most epoxidation methods in use today, it suffers from undesired epoxide opening caused by the slight acidity of the reaction milieu. Although acid-catalyzed side reactions can sometimes be minimized by use of buffered systems... [Pg.447]

Rosing, M. T., 1993, The buffering capacity of open heterogeneous systems. Geochimica et Cosmochimica Acta 57, 2223-2226. [Pg.528]

Fig. 23 Pseudo-first-order rate constants for the hydrolysis of NPAlk (n = 2-16) in the absence and in the presence of 1 as a function of alkanoate chain length n, catalyst concentration, and buffer system circles 7.5 x 10-5 molL-1 1 in Tris(hydroxymethyl)amino-methane (7ns) buffer solution closed up triangles 2.5 x 10-5 molL-1 1 in Tris buffer solution closed down triangles 2.5 x 10-5 molL-1 1 in phosphate buffer solution open squares 2.5 x 10-5 molL-1 1 in borate buffer solution open down triangles in Tris buffer solution only closed squares in phosphate buffer solution only open up triangles in borate buffer solution only. (Reprinted with permission from [73]. Copyright 1996 American Chemical Society)... Fig. 23 Pseudo-first-order rate constants for the hydrolysis of NPAlk (n = 2-16) in the absence and in the presence of 1 as a function of alkanoate chain length n, catalyst concentration, and buffer system circles 7.5 x 10-5 molL-1 1 in Tris(hydroxymethyl)amino-methane (7ns) buffer solution closed up triangles 2.5 x 10-5 molL-1 1 in Tris buffer solution closed down triangles 2.5 x 10-5 molL-1 1 in phosphate buffer solution open squares 2.5 x 10-5 molL-1 1 in borate buffer solution open down triangles in Tris buffer solution only closed squares in phosphate buffer solution only open up triangles in borate buffer solution only. (Reprinted with permission from [73]. Copyright 1996 American Chemical Society)...
Of course, during the transport process in the closed HLM system, the distribution ratio will change in accordance with changing feed and strip phase conditions (acidities, titanium concentration, etc.). At Kc = 1(Lf = Fr), concentration of titanium (IV) in the carrier solution should be [T1]r r (the system at equilibrium). Therefore, Lr may be denoted as an irreversible coefficient of the HLM for both, closed and open [78] systems (flowing feed, strip streams, buffered acidities, etc.). Kc is an uphill pumping border of the HLM system. [Pg.379]

Many naturally occurring systems are able to maintain a constant pH value by making use of buffer systems. In blood the hydrogencarbonate and protein systems maintain a pH 7.4. In open ocean water the pH is kept within the range 7.9-8.3 by a multicomponent buffer that includes aluminosilicates and carbonates. [Pg.313]

The pH value of the lachrymal fluid is about 7.4. Due to evaporation of CO2 from the tear film when the eyes are open, the pH value increases to 8 and even higher values [52]. Three buffer systems are present in tear fluid bicarbonate-carbonate, mono-dibasic phosphate and amphoteric proteins the buffer capacity is low [53]. The acid-neutralising capacity of the tear fluid of one eye is equal to about 8-10 microlitres 0.01 M NaOH. [Pg.169]

As we discussed in the opening section of this chapter, blood contains several buffering systems, the most important of which consists of carbonic acid and the carbonate ion. The concentrations of these buffer components in normal blood plasma are [HC03 ] = 0.024 M and [H2CO3] = 0.0012 M. The p fj, for carbonic acid at body temperature is 6.1. If we substitute these quantities into the Henderson-Hasselbalch equation, we can calculate the normal pH of blood ... [Pg.768]

The diazotization of amino derivatives of six-membered heteroaromatic ring systems, particularly that of aminopyridines and aminopyridine oxides, was studied in detail by Kalatzis and coworkers. Diazotization of 3-aminopyridine and its derivatives is similar to that of aromatic amines because of the formation of rather stable diazonium ions. 2- and 4-aminopyridines were considered to resist diazotization or to form mainly the corresponding hydroxy compounds. However, Kalatzis (1967 a) showed that true diazotization of these compounds proceeds in a similar way to that of the aromatic amines in 0,5-4.0 m hydrochloric, sulfuric, or perchloric acid, by mixing the solutions with aqueous sodium nitrite at 0 °C. However, the rapidly formed diazonium ion is hydrolyzed very easily within a few minutes (hydroxy-de-diazonia-tion). The diazonium ion must be used immediately after formation, e. g., for a diazo coupling reaction, or must be stabilized as the diazoate by prompt neutralization (after 45 s) to pH 10-11 with sodium hydroxide-borax buffer. All isomeric aminopyridine-1-oxides can be diazotized in the usual way (Kalatzis and Mastrokalos, 1977). The diazotization of 5-aminopyrimidines results in a complex ring opening and conversion into other heterocyclic systems (see Nemeryuk et al., 1985). [Pg.20]

In Figure 2 the solubility and speciation of plutonium have been calculated, using stability data for the hydroxy and carbonate complexes in Table III and standard potentials from Table IV, for the waters indicted in Figure 2. Here, the various carbonate concentrations would correspond to an open system in equilibrium with air (b) and closed systems with a total carbonate concentration of 30 mg/liter (c,e) and 485 mg/liter (d,f), respectively. The two redox potentials would roughly correspond to water in equilibrium wit air (a-d cf 50) and systems buffered by an Fe(III)(s)/Fe(II)(s)-equilibrium (e,f), respectively. Thus, the natural span of carbonate concentrations and redox conditions is illustrated. [Pg.284]

The mobile phase supply system consists of a series of reservoirs normally having a capacity ranging from 200 ml to 1,000 ml. Two reservoirs are the minimum required and are usually constructed of glass and fitted with an exit port open to air. Stainless steel is an alternative material for reservoir construction but is not considered satisfactory for mobile phases buffered to a low pH and containing... [Pg.124]

The microalgae are cultured in bioreactors under solar or artiflcial light in the presence of carbon dioxide and salts. The bioreactors may be closed systems made of polyethylene sleeves rather than open pools. Optimal conditions for pigment production are low to medium light intensity and medium temperatures (20 to 30°C). Pigment extraction is achieved by cell breakage, extraction into water or buffered solution, and centrifugation to separate out the filtrate. The filtrate may then be partly purified and sterilized by microfiltration and spray dried or lyophilized. [Pg.411]

Step 2. The orifice O, is open. As the pressure in the buffer volume is close to the average pressure in the system, the pressure in the pulse tube is higher than the pressure in the buffer. Hence, the gas flows from the tube to the buffer. Since the rotary valve is still open at the high-pressure side of the compressor, the pressure in the tube remains pH. [Pg.150]

In the open system, the CO2 fugacity (Fig. 23.3) varies linearly over the reaction path from about 75 to a value of one, as we prescribed, tracing a path of lower fugacity than predicted for the closed system. To maintain the lower fugacity, the program allows CO2 to escape from the fluid into the external gas buffer (see Chapter 14). The pH (Fig. 23.1) follows a path of higher values than in a closed system, reflecting the loss of CO2, an acid gas. [Pg.346]


See other pages where Open buffer system is mentioned: [Pg.288]    [Pg.288]    [Pg.53]    [Pg.155]    [Pg.174]    [Pg.644]    [Pg.162]    [Pg.91]    [Pg.293]    [Pg.48]    [Pg.26]    [Pg.195]    [Pg.139]    [Pg.1658]    [Pg.155]    [Pg.142]    [Pg.79]    [Pg.274]    [Pg.334]    [Pg.392]    [Pg.454]    [Pg.448]    [Pg.363]    [Pg.487]    [Pg.313]    [Pg.222]    [Pg.223]    [Pg.222]    [Pg.222]    [Pg.224]    [Pg.291]    [Pg.380]   
See also in sourсe #XX -- [ Pg.84 ]




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Buffer system

Open system

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