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Oxyanions ionicity

Auner attributed their formation to dissociation of the siloxane to a zwitter-ionic species 95, followed by what appears to be a truly remarkable rearrangement. An alternative explanation for the formation of 94 involves the formation of the oxyanion 96 by the addition of f-butyllithium to the... [Pg.127]

Fig. 1.7. Ionic radius r, and charge z, of common forms of elements in water. The solid lines divide (a) elements with Z/r <0.03 pm-1, which form soluble hydrated cations such as Ca2+ (b) ones with 7Jr >0.12 pm-1, soluble as oxyanions such as S042 and (c) those of intermediate Z/r, which form oxides or hydroxides insoluble around neutral pH. (Reproduced with permission from P.A. Cox (1989), see Further Reading.)... Fig. 1.7. Ionic radius r, and charge z, of common forms of elements in water. The solid lines divide (a) elements with Z/r <0.03 pm-1, which form soluble hydrated cations such as Ca2+ (b) ones with 7Jr >0.12 pm-1, soluble as oxyanions such as S042 and (c) those of intermediate Z/r, which form oxides or hydroxides insoluble around neutral pH. (Reproduced with permission from P.A. Cox (1989), see Further Reading.)...
By batch description trials Organo- and inorganically- modified zealot was subjected up to 24 hr in distilled water, tap water and 2% Nalco aqueous solutions in laboratory shaken machine to demonstrate how strongly the examined oxyanions are bound on the modified zeolite. While only slightly chromate desorption in the maximum extent about 20 mg/L was observed, approximately one order higher arsenate desorption was found, corresponding to increased ionic strength in waters. However, in both cases ODA-clinoptilolite exhibited the lowest desorption characteristics. Here, the... [Pg.22]

The unprimed side of the substrate is held in place by a series of interactions with the protein. In addition to the observed ionic (D936) or hydrophobic SI interaction site (Y946, 1969, V991, F1013), the PI main chain is held by its interaction with the oxyanion hole (G918, D966). P2-P4 residues will presumably utilize un-... [Pg.272]

Hayes, KF. Papelis, C. Leckie, J.O. (1988) Modeling ionic strength Effects on anion adsorption at hydrous oxide/solution interfaces. J. Colloid Interface Sd. 78 717—726 Hayes, KF. Roe, A.L. Brown, G.E. Hodgson, KO. Leckie, J.O. Parks, G.A. (1987) In-situ X-ray absorption study of surface complexes Selenium oxyanions on a-FeOOH. Sdence 238 783-786... [Pg.588]

Cr ). Those with a high-ionic potential (>20) form soluble oxyanions e.g. phosphate, nitrate, sulfate). [Pg.264]

Anions (including metal oxyanions such as chromate) can also be adsorbed, as can anionic ligands (such as phosphates and sulfates), and dissolved or suspended humic substances (such as fulvic acids). The ionic strength and pH influence the sorption of anions since they compete with the OH- ions... [Pg.129]

Summarizing the observations on the ionic crystals it may be said that there is abundant evidence that reactions in the hot zone play an important part. Thus, any theory, such as the elastic-collision model which neglects specific chemical effects, e.g., reduction by NH4+ and H2O, or oxidation by C104, under the influence of the high local temperature," cannot ve a complete explanation of the data. In none of the studies of the hot-atom chemistry of a series of oxyanion salts, e.g., the permanganates, have correlations been established between the retention and... [Pg.277]


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