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Prussian blue j

V.D. Neff, Electrochemical oxidation and reduction of thin films of Prussian blue. J. Electrochem. Soc. 128, 886-887 (1978). [Pg.454]

A.A. Karyakin and M.F. Chaplin, Polypyrrole-Prussian Blue films with controlled level of doping codeposition of polypyrrole and Prussian Blue. J. Electroanal. Chem. 370, 301-303 (1994). [Pg.459]

KanekoM., Takagashi K. and Tsuchida E. (1987), A photochargeable device composed of bilayer-membranes of poly(3-methylthiophene) and Prussian blue , J. Electroanal. Chem. 227, 255-258. [Pg.628]

C. Gabrielli, J.J. Garcia-Jareno, M. Keddam, H. Perrot, andF. Vicente, Ac-electrogravimetiy study of electroactive thin films. 1. Application to Prussian Blue. J. Phys. Chem. B, 106, 3182... [Pg.157]

J.G. Guan, Y.Q. Miao, and J.R. Chen, Prussian blue modified amperometric FIA biosensor one-step immunoassay for a-fetoprotein. Biosens. Bioelectron. 19, 789—794 (2004). [Pg.283]

J.E Keggin and F.D. Miles, Structure and formulae of the Prussian blue and related compounds. Nature 137, 577-578 (1936). [Pg.454]

A.A. Karyakin, E.E. Karyakina, and L. Gorton, The electrocatalytic activity of Prussian blue in hydrogen peroxide reduction studied using a wall-jet electrode with continuous flow. J. Electroanal. Chem. 456, 97-104 (1998). [Pg.454]

R. Yang, Z.B. Qian, and J.Q. Deng, Electrochemical deposition of Prussian blue from a single ferricya-nide solution. J. Electrochem. Soc. 145, 2231-2236 (1998). [Pg.454]

J.M. Zen, P.Y. Chen, and A.S. Kumar, Flow injection analysis of an ultratrace amount of arsenite using a Prussian blue-modified screen-printed electrode. Anal. Chem. 75, 6017-6022 (2003). [Pg.455]

T. Ikeshoji, Separation of alkali-metal ions by intercalation into a Prussian blue electrode. J. Electrochem. Soc. 133, 2108-2109 (1986). [Pg.456]

C. Gabrielli, P. Hemery, P. Liatsi, M. Masure, and H. Perrot, An electrogravimetric study of an all-solid-state potassium selective electrode with Prussian blue as the electroactive solid internal contact. J. Electrochem. Soc. 152, H219 (2005). [Pg.456]

H. Kahlert, S. Komorsky-Lovric, M. Hermes, and F. Scholz, Prussian blue-based reactive electrode (reactrode) for the determination of thallium ions. Fresenius J. Anal. Chem. 356, 204-208 (1996). [Pg.456]

J.M. Zen, H. Ho, and P.Y. Chen, Voltammetric determination of thallium on a Prussian blue/cinder paste electrode. Indian J. Chem. Sect. A Inorgan. Bio-Inorgan. Phys. Theoret. Anal. Chem. 42, 839—842 (2003). [Pg.456]

F. Ricci, F. Arduini, A. Amine, D. Moscone, and G. Palleschi, Characterisation of Prussian blue modified screen-printed electrodes for thiol detection. J. Electroanal. Chem. 563, 229—237 (2004). [Pg.457]

J.M. Zen, A.S. Kumar, and H.W. Chen, Electrochemical behavior of stable cinder/Prussian blue analogue and its mediated nitrite oxidation. Electroanalysis 13, 1171-1178 (2001). [Pg.457]

M.F. de Oliveira, R.J. Mortimer, and N.R. Stradiotto, Voltammetric determination of persulfate anions using an electrode modified with a Prussian blue film. Microchem. J. 64, 155-159 (2000). [Pg.458]

Q.J. Chi and S.J. Dong, Amperometric biosensors based on the immobilization of oxidases in a Prussian blue film by electrochemical codeposition. Anal. Chim. Acta 310, 429 436 (1995). [Pg.460]

X. Zhang, J. Wang, B. Ogorevc, and U.E. Spichiger, Glucose nanosensor based on Prussian-blue modified carbon-fiber cone nanoelectrode and an integrated reference electrode. Electroanalysis 11, 945-949 (1999). [Pg.460]

J.C. Vidal, J. Espuelas, E. Garda-Ruiz, and J.R. Castillo, Amperometric cholesterol biosensors based on the electropolymerization of pyrrole and the electrocatalytic effect of Prussian-Blue layers helped with self-assembled monolayers. Talanta 64, 655 (2004). [Pg.461]

J.P. Li, T.Z. Peng, and Y.Q. Peng, A cholesterol biosensor based on entrapment of cholesterol oxidase in a silicic sol-gel matrix at a Prussian blue modified electrode. Electroanalysis 15, 1031—1037 (2003). [Pg.461]

Figure 8.3 Illustration of in situ spectroelectrochemistry, showing a set of UV-vis ( electronic ) spectra of solid-state Prussian Blue (iron(ii,iii) hexacyanoferrate(ii)) adhered to an ITO-coated optically transparent electrode. The spectra are shown as a function of applied potential (i) —0.2 (ii) -1-0.5 (iii) -1-0.8 (iv) -1-0.85 (v) -1-0.9 (vi) +1.2 V (all vs. SCE). From Mortimer, R. J. and Rosseinsky, D. R., J. Chem. Soc., Dalton Trans., 2059-2061 (1984). Reproduced by permission of The Royal Society of Chemistry. Figure 8.3 Illustration of in situ spectroelectrochemistry, showing a set of UV-vis ( electronic ) spectra of solid-state Prussian Blue (iron(ii,iii) hexacyanoferrate(ii)) adhered to an ITO-coated optically transparent electrode. The spectra are shown as a function of applied potential (i) —0.2 (ii) -1-0.5 (iii) -1-0.8 (iv) -1-0.85 (v) -1-0.9 (vi) +1.2 V (all vs. SCE). From Mortimer, R. J. and Rosseinsky, D. R., J. Chem. Soc., Dalton Trans., 2059-2061 (1984). Reproduced by permission of The Royal Society of Chemistry.
Prussian blue (inorgchem) Fe4 Fe(CN)6 3 Ferric ferrocyanide, used as a blue pigment and in the removal of hydrogen sulfide from gases. prash an blu j prussic acid See hydrocyanic acid. pras ik as ad ... [Pg.313]

Graham HD (1992) Stabilization of the Prussian blue color in the determination of polyphenols. J Agric Food Chem 40 801-805... [Pg.46]

S. Kumar, J.-M. Zen, Unusual Redox Catalysis in a Ruthenium Oxide-Prussian blue Combined Material, Chem. Phys. Chem. 5 (2004) 1227-1231. [Pg.368]

C j 4 alkyl group) 0.5—8.0%, and binder 15—45%. The binder contains 15—45% polymeric material, such as poly (vinyl acetate) or polyfvinyl chloride) with the lower alkyl esters of NC and 65— 85% oxygenated hydrocarbon plasticizers (such as lower alkylene glycols their oxalates, maleates, diglycolates or nitrodiphenyl ethers, etc). E.g. AN 78, Prussian Blue 3, N-amino-alkylmorpholine 3) binder 12, carbon black 3 MgO I%]... [Pg.560]

Prussian blue is regarded as a compound of three equivalents of ferroeyanogen with two of iron, and its composition is therefore expressed by the formula 8 Cfy -j- 2 Fea, or Fe, Cys, It is formed whenever a salt of sesquioxide of iron is added to a soluble metallio ferrocyanide. The usual method is to precipitate a solution of sesquiehloride or sesquinitrate of iron by ferrocyanide of potassium and In point qf fact a very important part of its manufacture consists in the preparation of this latter salt, which will now be described. [Pg.451]

Fig. 12.47 Portion of Ihe crystal structure of Prussian blue showing the bridging by ambidentate cyanide ions. Circles represent iron(II) (O). iron(UI) (O), and oxygen in water ( ). The remaining interstitial or "zeoiitic" water in the cubic sites has been omitted for clarity, as hove most of the cyanide ious. In addition, some of the cyanide ions are replaced by water molecules coordinated to iron(III), and there are also vacancies in the structure. [Modified from Buser, H. J. Schwarzenbach, D. Petter, W. Ludi, A. Inorg. Chem. 1977, 16. 2704-2710. Reproduced with permission.]... Fig. 12.47 Portion of Ihe crystal structure of Prussian blue showing the bridging by ambidentate cyanide ions. Circles represent iron(II) (O). iron(UI) (O), and oxygen in water ( ). The remaining interstitial or "zeoiitic" water in the cubic sites has been omitted for clarity, as hove most of the cyanide ious. In addition, some of the cyanide ions are replaced by water molecules coordinated to iron(III), and there are also vacancies in the structure. [Modified from Buser, H. J. Schwarzenbach, D. Petter, W. Ludi, A. Inorg. Chem. 1977, 16. 2704-2710. Reproduced with permission.]...
Cyanide Iron Blues. Cyanide iron blue, also known as Prussian blue, is one of die oldest industrially produced, inorganic pigments. Chemically, cyanide iron blues are based on the Fe21 [Fe31 (CN)g]J anion. The charge is balanced by sodium, potassium, or ammonium cations. [Pg.1307]

All of the [Fe(CN) J4- salts may be considered salts of ferrocyanic acid or tetrahydrogen hexakiscyanoferrate [17126-47-5], H4[Fe(CN)J, a strongly acidic, air-sensitive compound. It is soluble in water and alcohol but is insoluble in ether. It can be prepared by precipitation of an etherate by adding ether to a solution of [Fe(CN) J4"" that was acidified with concentrated sulfuric acid. Removal of the ether of solvation affords a white powder which is stable when dry but slowly turns blue in moist air because of Prussian Blue formation. [Pg.435]

Prussian Blue. Reaction of [Fe(CN)6]4 with an excess of aqueous iron(III) produces the finely divided, intensely blue precipitate Prussian Blue [14038-43-8] (tetrairon(III) tris(hexakiscyanoferrate)), Fe4fFe(CN)6]. Prussian Blue is identical to Turnbull s Blue, the name which originally was given to the material produced by reaction of [Fe(CN)6]3 with excess aqueous iron(II). The solid contains or has absorbed on its surface a laige and variable number of water molecules, potassium ions (if present in the reaction), and iron(III) oxide. The iron(II) centers are low spin and diamagnetic iron(III) centers are high spin. Variations of composition and properties result from variations in reaction conditions. Rapid precipitation in the presence of potassium ion affords a colloidal suspension of Prussian Blue [25869-98-1] which has the approximate composition IvFe[Fe(CN) J. Prussian Blue compounds are used as pigments in inks and paints and its formation on sensitized paper is utilized in the production of blueprints. [Pg.435]


See other pages where Prussian blue j is mentioned: [Pg.54]    [Pg.54]    [Pg.397]    [Pg.670]    [Pg.454]    [Pg.457]    [Pg.139]    [Pg.254]    [Pg.255]    [Pg.255]    [Pg.256]    [Pg.297]    [Pg.1058]   
See also in sourсe #XX -- [ Pg.299 , Pg.379 ]




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