The Pecularity Of Sorption Of Some Toxic Ions

THE PECULARITY OF SORPTION OF SOME TOXIC IONS

BY ALUMINIUM HYDROPHOSPHATES PREPARED

BY SOL–GEL TECHNOLOGY

V. V. Strelko, V. A. Kanibolotsky, A. A. Zaitseva,

S. I. Meleshevich, N. I.Chubar

Institute for Sorption and Endoecology Problems,

National Academy of Sciences of Ukraine, Kyiv, Ukraine

The new sol-gel method of synthesis of aluminium hydrooxides was elaborated, in which simple and accesible chemicals - inorganic aluminium salts, acides and bases - were used, instead of traditionally used in sol-gel synthesis expensive and unsafe in using organic derivatives of metales. The optimum conditions for formations of aluminium hydrophosphates gels, contained different amounts of phosphates and hydrooxides groups, were worked out, using indicated substances. The influence of different factors, such as temperature of synthesis, concentration and ratio of reagents and so on, to process of gels formation and physico-chemical properties of obtained gels was studed, and the best conditions for gels coagulation, washing and drying of sorbents were determined.

The influence of ratio between phosphate and hydrooxide groups to sorption and chemical properties of obtained aluminium hydrophosphate sorbents was investigated, and the best ratio were determined for sorptin of the number of ions. To study ionexchange properties of sorbents curves of potentiometric titration were reserched. The pecularity of sorption of cation and anion forms of some ions, such as anions CrO42-, AsO42-, cations Cu2+ and so on, which are priority contaminaters, was detaily investigated; the influence of quantity of ionexchange capacity to pH and sorption kinetics indicated ions were reserched. The high affinity of aluminium hydrophosphate sorbents to anions of CrO42-, AsO42- was received.

The data of porometric characteristic, results of IR- and X-ray studies of obtainen aluminium hydrophosphate sorbents are represented.



Related articles::

  • Comparative Assessment Of Sorption
  • Kinetics Of Sorption Of Cr((vi)-diphenylcarbazide Complex On Ku-2-8 Cation Exchanger
  • The Study Of Dinamic Sorption Oil And Oil Products From Water Medium By Carbon Sorbents Based
  • The Influence Of Surface Chemistry Of Synthetic Sorption Materials On Deriving By Its Modified
  • Influence Of Humic Substances On The Sorption
  • Selective Sorption Of Heavy Metal Ions
  • Sorption And Photochemical Activity
  • New Sorbents Based On Modified Silica
  • Experimental Study Of Uranium Sorption Onto Biological Substrates
  • Sorption Of Uranium
  • Selective Separation Of Borate Ions In Water
  • The Studies On The Removal Of Nickel(ii) And Cobalt(ii) Ions From The Aminopolycarboxylic Acid Solutions On The Amberlite Ira 958, Amberlite Ira 458
  • H+-mg2+ And H+-ca2+ Exchange Onto Carboxylic Ionites In Terms Of The Exchange Equilibrium Theory
  • The Photocatalytic Activity Of Tio2 Samples, Modyfing By Co, Cr, Cu And Fe Cations In Reaction
  • Development Of The Modified Sorbents
  • Modified Organosilica Sorbents
  • Concentrating And Separating Of Al(iii), Ga(iii) And In(iii) By Their Sorption On Amorphous Silicas
  • Sorption Of Ni (ii) And Co (ii) Ions From Water Solution By Strong-acid Cationite Cu-2-8n
  • Uranium Extraction By Amorphous Modified Titanium And Zirconium Phosphates
  • Adsorption And Ion-exchange From Aqueous Solutions Under Magnetic Field Influence
  • Titanium – Manganese Oxides. Synthesis,
  • Part Of The Sorption In Tdpc And Mb Photocatalytic Destruction Processes
  • Regeneration Of Carboxylic Acrylic Cationexchange Resins By Stochiometric Amount
  • Sorption Of Silicon Tetrafluoride
  • Synthesis And Ion-exchange Properties Of Novel Materials On The Basis Of Zirconium (iv) Hydroxophosphates With A Hydroxyethylidenediphosphonic Acid
  • Modification Of Structure And Properties
  • Study Of Ion-exchange Properties Of Clinoptilolite, Modified By Titanium Phosphates
  • Theoretical And Experimental Studies
  • Electroregeneration Of Ni (ii) -loaded
  • Studies Of The Electrochemical Activity Of Thiobensoalides At The Mercuty Electrode