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Phosphate electrolytes

Fig. 27.3. Voltammograms of silver oxidation from conjugate localized on transducer. Background electrolyte Phosphate buffer solution pH = 7.2. Protein A concentration 10 and 15 pg/ml (1) lOOpg/ml (2) 70 pg/ml (3) 50 pg/ml (4). Fig. 27.3. Voltammograms of silver oxidation from conjugate localized on transducer. Background electrolyte Phosphate buffer solution pH = 7.2. Protein A concentration 10 and 15 pg/ml (1) lOOpg/ml (2) 70 pg/ml (3) 50 pg/ml (4).
Figure 4.9. RDE voltammograms response of Mb/DDAB film modified GCE around the Pglll/Il couple in the presence of various nitrite concentrations. Curve (a) 2.0 mM (b) 4.0 mM (c) 6.0 mM (d) 8.0 mM. Electrolyte phosphate buffer solution, 50 mM NaBr (pH = 7.4). Rotation rate 500 rpm scan rate 0.02 Vs ... Figure 4.9. RDE voltammograms response of Mb/DDAB film modified GCE around the Pglll/Il couple in the presence of various nitrite concentrations. Curve (a) 2.0 mM (b) 4.0 mM (c) 6.0 mM (d) 8.0 mM. Electrolyte phosphate buffer solution, 50 mM NaBr (pH = 7.4). Rotation rate 500 rpm scan rate 0.02 Vs ...
Figure 5.13. Voltammetric response of a glassy carbon (A), 4-aminopyridine-electrode (B), and the supramolecular electrode (formed by packed Co(II) benzoporphyrins) (C) under N2 (continuous line) and CO2 (dashed line). Scan rate 0.05 V s . Electrolyte phosphate/biphosphate (pH 6.8 under N2, pH 5.2 under C02) buffered aqueous solution. Reprinted from Figure 4A (A), Figure 4B (B) and Figure 5(C) G. Ramirez, M. Lucero, A. Riquekne, M. Villagran, J. Costamagna, E. TroUund and M.J. Aguirre, A supramolecular Cobaltporph5Tin-modified electrode toward the electroreduction of CO2, Journal Coordination Chemistry, 57 (2004) 249-255. With permission of Taylor and Francis (http //www.tandf.co.uk/journal). Figure 5.13. Voltammetric response of a glassy carbon (A), 4-aminopyridine-electrode (B), and the supramolecular electrode (formed by packed Co(II) benzoporphyrins) (C) under N2 (continuous line) and CO2 (dashed line). Scan rate 0.05 V s . Electrolyte phosphate/biphosphate (pH 6.8 under N2, pH 5.2 under C02) buffered aqueous solution. Reprinted from Figure 4A (A), Figure 4B (B) and Figure 5(C) G. Ramirez, M. Lucero, A. Riquekne, M. Villagran, J. Costamagna, E. TroUund and M.J. Aguirre, A supramolecular Cobaltporph5Tin-modified electrode toward the electroreduction of CO2, Journal Coordination Chemistry, 57 (2004) 249-255. With permission of Taylor and Francis (http //www.tandf.co.uk/journal).
Figure 10.2 Cyclic voltammogram of oxidation of 2.5x10" m dopamine in the presence of 100-fold excess of ascorbic acid, in phosphate buffer, pH = 7, obtained on (a) bare carbon fibre microdisc electrode and (b) the same electrode modified with semipermeable membrane poly(4-HBS/2-AP) (100 1). Curves ( ) were obtained in the background electrolyte (phosphate buffer, pH = 7). Figure 10.2 Cyclic voltammogram of oxidation of 2.5x10" m dopamine in the presence of 100-fold excess of ascorbic acid, in phosphate buffer, pH = 7, obtained on (a) bare carbon fibre microdisc electrode and (b) the same electrode modified with semipermeable membrane poly(4-HBS/2-AP) (100 1). Curves ( ) were obtained in the background electrolyte (phosphate buffer, pH = 7).
Phosphoric Acid Fuel Cell. Concentrated phosphoric acid is used for the electrolyte ia PAFC, which operates at 150 to 220°C. At lower temperatures, phosphoric acid is a poor ionic conductor (see Phosphoric acid and the phosphates), and CO poisoning of the Pt electrocatalyst ia the anode becomes more severe when steam-reformed hydrocarbons (qv) are used as the hydrogen-rich fuel. The relative stabiUty of concentrated phosphoric acid is high compared to other common inorganic acids consequentiy, the PAFC is capable of operating at elevated temperatures. In addition, the use of concentrated (- 100%) acid minimizes the water-vapor pressure so water management ia the cell is not difficult. The porous matrix used to retain the acid is usually sihcon carbide SiC, and the electrocatalyst ia both the anode and cathode is mainly Pt. [Pg.579]

Electrolyte is added to the recipe to help control particle size of the latex produced. Materials like sodium carbonate or trisodium phosphate are commonly used. [Pg.520]

Electrochemical Process. Several patents claim that ethylene oxide is produced ia good yields ia addition to faradic quantities of substantially pure hydrogen when water and ethylene react ia an electrochemical cell to form ethylene oxide and hydrogen (206—208). The only raw materials that are utilized ia the ethylene oxide formation are ethylene, water, and electrical energy. The electrolyte is regenerated in situ ie, within the electrolytic cell. The addition of oxygen to the ethylene is activated by a catalyst such as elemental silver or its compounds at the anode or its vicinity (206). The common electrolytes used are water-soluble alkah metal phosphates, borates, sulfates, or chromates at ca 22—25°C (207). The process can be either batch or continuous (see Electrochemicalprocessing). [Pg.461]

Electrolysis at a Hg cathode, -1.2 V (Ag wire), CH3CN, DMF, Bu4N Bp4", 2,6-lutidine." LiCl or LiC104 have been used as electrolytes in the electrochemical removal of haloethyl phosphates. ... [Pg.681]

A 0-9% salt solution is considered to be isotonic with blood. Other electrolytes present include bicarbonate ions (HCOj ) and small amounts of potassium, calcium, magnesium, phosphate, sulphate and organic acid ions. Included among the complex compounds and present in smaller amounts are phospholipids, cholesterols, natural fats, proteins, glucose and amino acids. Under normal conditions the extracellular body fluid is slightly alkaline with a pH of 7-4. ... [Pg.472]

It has been established that in the case of electrolytes, such as boric acid or ammonium phosphate solutions, in which aluminium oxide is insoluble. [Pg.689]

A large number of electrolytic treatments of magnesium, anodic or a.c., have been developed, in which adherent white or grey films consisting of fluoride, oxide, hydroxide, aluminate or basic carbonate are deposited from alkaline solutions containing caustic alkali, alkali carbonates, phosphates, pyrophosphates, cyanides, aluminates, oxalates, silicates, borates, etc. Some films are thin, and some are relatively thick. All are more or less absorbent and act as good bases for paint, though none contributes appreciable inhibition. All can, however, absorb chromates with consequent improvement of protective efficiency. [Pg.729]

The action is rapid, and the acidity of the electrolyte is unaffected. The error due to nitrous acid is increased by the presence of a large amount of iron iron is reduced by the current to the iron(II) state, whereupon the nitric acid is reduced. This error may be minimised by the proper regulation of the pH and by the addition of ammonium nitrate instead of nitric acid, or, best, by the removal of the iron prior to the electrolysis, or by complexation with phosphate or fluoride. [Pg.515]

Reagents. Supporting electrolyte. Prepare a 0.1M phosphate buffer of pH = 8 containing 0.1M potassium iodide and 0.025 M potassium tartrate (0.17 g Na2HP04,12H20, 3.38 g NaH2P04,2H20, 4.15 g KI and 1.5 g potassium tartrate, in 250 mL of water). [Pg.541]

In men, administration of an androgen may result in breast enlargement (gynecomastia), testicular atrophy, inhibition of testicular function, impotence, enlargement of the penis, nausea, jaundice, headache, anxiety, male pattern baldness, acne, and depression. Fluid and electrolyte imbalances, which include sodium, water, chloride, potassium, calcium, and phosphate retention, may also be seen. [Pg.540]

Ether carboxylates are used not only in powdered detergents but in liquid laundry detergents for their hard water stability, lime soap dispersibility, and electrolyte stability they improve the suspension stability and rheology of the electrolyte builder [130,131]. Formulations based particularly on lauryl ether carboxylate + 4.5 EO combined with fatty acid salt and other anionic surfactants are described [132], sometimes in combination with quaternary compounds as softeners [133,163]. Ether carboxylates show improved cleaning properties as suds-controlling agents in formulations with ethoxylated alkylphenol or fatty alcohol, alkyl phosphate esters or alkoxylate phosphate esters, and water-soluble builders [134]. [Pg.339]

In a typical equilibrium dialysis study of charged polysaccharides an indicator ion, L (chromate), is included in the supporting electrolyte medium (phosphate buffer, pH 6.8, I 0.08) to allow assessment of the effective net charge of the polyanions via a modified form of Eq. 31, namely. [Pg.248]

Fluorinated phosphonates exhibit interesting properties as enzyme inhibitors, chelating agents or as fuel cell electrolytes [29] however, only few methods of preparation for these compounds are available. Burton et al. [30] developed several methods to prepare fluorinated phosphates which involve phosphonyl, and likely phosphoranyl radicals as chain carriers (Scheme 11). [Pg.50]


See other pages where Phosphate electrolytes is mentioned: [Pg.1324]    [Pg.233]    [Pg.941]    [Pg.474]    [Pg.1324]    [Pg.233]    [Pg.941]    [Pg.474]    [Pg.99]    [Pg.487]    [Pg.227]    [Pg.579]    [Pg.130]    [Pg.462]    [Pg.3]    [Pg.536]    [Pg.49]    [Pg.244]    [Pg.99]    [Pg.100]    [Pg.388]    [Pg.520]    [Pg.1057]    [Pg.560]    [Pg.690]    [Pg.708]    [Pg.86]    [Pg.12]    [Pg.684]    [Pg.826]    [Pg.97]    [Pg.158]    [Pg.103]    [Pg.117]    [Pg.95]    [Pg.32]   
See also in sourсe #XX -- [ Pg.52 , Pg.64 , Pg.66 ]




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