J 2010

Adsorption of mercury species on river sediments - effects of selected abiotic parameters

PELCOVÁ, Pavlína; Jana MARGETINOVÁ; Tomáš VACULOVIČ; Josef KOMÁREK; Vlastimil KUBÁŇ et al.

Základní údaje

Originální název

Adsorption of mercury species on river sediments - effects of selected abiotic parameters

Název česky

Adsorpce spécií rtuti v říčním sedimentu - vliv vybraných abiotických parametrů

Autoři

PELCOVÁ, Pavlína; Jana MARGETINOVÁ; Tomáš VACULOVIČ; Josef KOMÁREK a Vlastimil KUBÁŇ

Vydání

Central European Journal of Chemistry, Heidelberg, Versita Warsaw and Springer-Verlag Berli, 2010, 1895-1066

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10406 Analytical chemistry

Stát vydavatele

Polsko

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 0.991

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14310/10:00044388

Organizační jednotka

Přírodovědecká fakulta

Klíčová slova anglicky

Mercury species; Adsorption; River sediments
Změněno: 23. 7. 2010 18:31, doc. Mgr. Tomáš Vaculovič, Ph.D.

Anotace

V originále

Abiotic parameters (pH, temperature, current velocity, mercury species concentration, and sediment and aqueous media composition) influence mercury species (MeHg+, EtHg+, PhHg+ and inorganic Hg2+) adsorption on river sediments. The highest amount of adsorbed MeHg+ and EtHg+ (82-93% and 85-91% for static and agitated system, respectively) occurred at pH 3-4. For PhHg+ the maximum adsorption (90% and 95% for static and agitated systems) was located over the broad 3-10 pH range, while for Hg2+ (94% and 97% for static and agitated systems) it was at pH similar to 3. Temperature (4.5-60 degrees C) influenced the adsorption rate but not the quantity. Both rate and quantity increased in the order: static < agitated <= stirred systems. The aqueous medium composition affected both rate and quantity. Sulfate caused the largest adsorption decrease for organomercury species (15-25% decrease); sulfide reduced Hg2+ adsorption about 67%. Cations at pH 5.2 reduced either the adsorption rate (Ca2+, Al3+) or the total adsorption (Zn2+, Fe3+). Positive correlations were found between sediment C, N, S content as well as cation exchange capacity (CEC) with mercury adsorption (R = 0.45-0.66, 0.56-0.89, 0.45-0.61 and 0.55-0.73, respectively) while negative correlations were observed with Fe and Al (R = -0.63 to -0.90 and -0.65 to -0.86, respectively)

Česky

Abiotic parameters (pH, temperature, current velocity, mercury species concentration, and sediment and aqueous media composition) influence mercury species (MeHg+, EtHg+, PhHg+ and inorganic Hg2+) adsorption on river sediments. The highest amount of adsorbed MeHg+ and EtHg+ (82-93% and 85-91% for static and agitated system, respectively) occurred at pH 3-4. For PhHg+ the maximum adsorption (90% and 95% for static and agitated systems) was located over the broad 3-10 pH range, while for Hg2+ (94% and 97% for static and agitated systems) it was at pH similar to 3. Temperature (4.5-60 degrees C) influenced the adsorption rate but not the quantity. Both rate and quantity increased in the order: static < agitated <= stirred systems. The aqueous medium composition affected both rate and quantity. Sulfate caused the largest adsorption decrease for organomercury species (15-25% decrease); sulfide reduced Hg2+ adsorption about 67%. Cations at pH 5.2 reduced either the adsorption rate (Ca2+, Al3+) or the total adsorption (Zn2+, Fe3+). Positive correlations were found between sediment C, N, S content as well as cation exchange capacity (CEC) with mercury adsorption (R = 0.45-0.66, 0.56-0.89, 0.45-0.61 and 0.55-0.73, respectively) while negative correlations were observed with Fe and Al (R = -0.63 to -0.90 and -0.65 to -0.86, respectively)

Návaznosti

MSM0021622412, záměr
Název: Interakce mezi chemickými látkami, prostředím a biologickými systémy a jejich důsledky na globální, regionální a lokální úrovni (INCHEMBIOL) (Akronym: INCHEMBIOL)
Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Interakce mezi chemickými látkami, prostředím a biologickými systémy a jejich důsledky na globální , regionální a lokální úrovni