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Badanie fizykochemicznych właściwości chemicznie modyfikowanych węgli aktywnych

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EN
Study of physicochemical properties of chemically modified activated carbons
Języki publikacji
PL
Abstrakty
PL
Badano fizykochemiczne właściwości węgli aktywnych otrzymanych przez modyfikację węgla handlowego poprzez osadzanie depozytu węglowego z rozkładu chlorku metylenu. Na podstawie niskotemperaturowej adsorpcji azotu wyznaczono podstawowe parametry struktury porowatej. Stosując metodę Boehma, wyznaczono stężenie powierzchniowych grup funkcyjnych zawierających tlen. Metodą inwersyjnej chromatografii gazowej (IGC) wyznaczono izotermy adsorpcji alkoholi alifatycznych od C=1 do C=4 oraz benzenu i chloroformu. Na podstawie otrzymanych izoterm adsorpcji obliczono wartości izosterycznego ciepła adsorpcji qst. Stwierdzono istotny wpływ depozytu węglowego na właściwości strukturalne i powierzchniowe węgla aktywnego.
EN
Physicochemical properties of activated carbons prepared by chemical modification of a commercial active carbon were studied. The modification consisted in forming so-called carbon deposit from methylene chloride pyrolysis. The obtained modified activated carbons contained carbon deposit within the range of 7.28 to 20.91% by weight. The basic parameters of porous structure were calculated by means of low-temperature nitrogen adsorption. The specific surface, determined by BET method within the range of relative pressures (p/p0 0.01 to 0.2, is going down regularly from 790 m2/g (the commercial carbon) to 360 m2/g (the carbon containing 20.91% by weight carbon deposit). Moreover, the micropore volume (calculated by means Barrett, Joyner and Halenda method) changes also regularly from 0.34 to 0.15 cm3/g, similarly as total pore volume from 0.40 to 0.19 cm3/g. The results point out that, forming a carbon deposit has a great influence on the pore structure of the carbon materials, and during the modification adsorptive properties to nitrogen are getting worse markedly. Using the Boehm method the concentration of surface acidic functional groups containing oxygen such as: carboxylic, lactic, carbonyl and phenyl groups, were determined. The total concentration of surface functional groups is almost the same for the studied carbons except carbon possessing 20.91% by weight carbon deposit (here the concentration is smaller). On the other hand, the carbons differ in the concentration of individual groups. This effect is most visible in the concentration of carboxylic groups: the commercial carbon contains 0.016 mmol/g carboxylic groups and the all modified carbons contain about 0.55 mmol/g of these groups. Adsorption isotherms of aliphatic alcohols (C=1 to C=4), benzene and trichloromethane on all studied carbons were determined by means of inverse gas chromatography (IGC). The measurements were carried out by a Mera-Elmet type N-504 chromatograph, using a thermoconductometic detector (TCD), helium as a carrier gas, within the temperature range from 333 to 493 K. The adsorption isotherms were calculated by the peak profile method by graphic integration of an individual chromatogram. The measurements of adsorption isotherms at various temperatures permit to calculate isosteric adsorption heat (qst). It can be said generally that the isosteric adsorption heat is going up with the degree of surface covering. If the degree of surface covering is small, the magnitude of heat effect depends mainly on interaction between adsorbate-adsorbent. Whereas for the increasing degree of surface covering there can be additional adsorbate--adsorbate interaction. Additionally, the molecules of aliphatic alcohols can create hydrogen bonds with the carbon surface having adequate surface functional groups. The obtained values of isosteric adsorption heats are about 60 kJ/mol to the extent of degree of surface covering to 30 μmol/g. It can suggest that the dominant adsorption mechanism is physical adsorption.
Rocznik
Strony
5--17
Opis fizyczny
Bibliogr. 13 poz.
Twórcy
  • Akademia Świętokrzyska, Instytut Chemii, ul. Chęcińska 5, 25-020 Kielce
autor
  • Akademia Świętokrzyska, Instytut Chemii, ul. Chęcińska 5, 25-020 Kielce
Bibliografia
  • [1] Jankowska H., Świątkowski A., Choma J., Węgiel aktywny, PWN, Warszawa 1985.
  • [2] Shin S., Jang J., Yoon S.H., Mochida I., A study on the effect of heat treatment on functional groups of pitch based activated carbon using FTIR, Carbon 1997, 35, 12, 1739-1743.
  • [3] Pradha B.K., Sondle N.K., Effect of different oxidizing agent treatments on the surface properties of activated carbons, Carbon 1999, 37, 8, 1323-1332.
  • [4] El-Hendawy A.A., Influence of HN03 on oxidation the structure and adsorptive properties of corncob - based activated carbon, Carbon 2003, 41, 4, 713-722.
  • [5] Leboda R., Investigation of active carbon texture modification, Chem. Stosów. 1989, 33, 1, 35-45.
  • [6] Gierak A., Leboda R., The thermal properties of carbon - silica adsorbents (carbosils) by methylene chloride pyrolysis, J. Therm. Anal. 1989, 35, 7, 2213-2224.
  • [7] Leboda R., Łodyga A., Studies on the application of Polish commercial active carbons in chromatography. Preparation and properties of adsorbents for separation of low-boiling compounds, Chem. Anal. 1991, 36, 1, 103-109.
  • [8] Dąbek L., Slomkiewicz P., Zieliński W., An effect of modification of activated carbons with a carbon deposit on their properties as carriers for catalysts in synthesis of vinyl acetate from acetylene and acetic acid, Pol. J. Appl. Chem. 1993, 37, 3-4, 255-261.
  • [9] Dąbek L., Repelewicz M., Zdenkowski J., Zastosowanie węgla aktywnego oraz jego modyfikatów do usuwania węglowodorów aromatycznych z wód podziemnych skażonych substancjami ropopochodnymi, Inżynieria i Ochrona Środowiska 2000, 3, 3-4, 415-420.
  • [10] Dąbek L., Repelewicz M., Wpływ modyfikacji depozytem węglowym na strukturę porowatą oraz własności mechaniczne węgli aktywnych, Karbo-Energochemia-Ekologia 1994, 39, 8, 201-204.
  • [11] Contescu A., Contescu C, Putyera K., Schwarz J.A., Surface acidity of carbons characterized by their continuous pK distribution and Boehm titration, Carbon 1997, 35, 1, 83-94.
  • [12] Charmas B., Leboda R., Effect of surface heterogeneity on adsorption on solid surfaces: Application of inverse gas chromatography in the studies of energetic heterogeneity of adsorbents, J. Chromatography A 2000, 886, 133-152.
  • [13] Papirer E., Brendle E., Ozil F., Baiard H., Comparison of surface properties of graphite, carbon black and fullerene samples, measured by inverse gas chromatography, Carbon 1999, 37, 8, 1265-1274.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-LOD3-0001-0001
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