Chemical Engineering / Kimya Mühendisliği

Permanent URI for this collectionhttps://hdl.handle.net/11147/14

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  • Article
    Citation - WoS: 11
    Citation - Scopus: 11
    Effect of Different Acidity Modifications on the Activity and Selectivity on H-Zsm5 Zeolites in N-Butene Isomerization
    (Springer Verlag, 2014) Kılıç, Emre; Yılmaz, Selahattin
    H-ZSM-5 was modified by silylation [tetraethylorthosilicate (TEOS) and triaminopropyltriethoxysilane], alkali (NaOH), acid (HCl) and ammoniumhexafluorosilicate (AHFS) treatments. The parent and modified zeolite forms were tested in n-butene isomerization. Modifications affected total acidities, the strength of the acid sites, pore sizes and surface areas of the H-ZSM-5 differently. The modifications decreased the conversion obtained by the parent catalyst. TEOS and alkali modifications did not promote formation of isobutene. Pre-alkali treatment before acid treatment increased selectivity to isobutene from 56.0 to 66.7 %, while conversion changed a little, it dropped from 52 to 50 %. AHFS modification provided the highest enhancement in selectivity to isobutene (87.5 %) for which n-butene conversion was dropped by about 10 % compared to H-ZSM-5. This was attributed to a slight modification of the pore size and to the reduction in strong and weak acid sites and generation of new Lewis acid sites.
  • Article
    Citation - WoS: 14
    Citation - Scopus: 15
    Neutralization of an Extremely Acidic Sludge and Stabilization of Heavy Metals in Flyash Aggregates
    (Elsevier Ltd., 2007) Polat, Mehmet; Güler, Erkan; Lederman, Eli; Cohen, Haim
    An extremely acidic, heavy metal-rich sludge (pH = -1.2) was scrubbed with a Class-F fly ash in order to simultaneously neutralize the acidity and stabilize the heavy metals contained in both wastes. This paper outlines the leaching behavior of the aggregate material generated by scrubbing. For proper fly ash/sludge ratios, the fly ash acted as an outstanding neutralizer for the acidic waste. Leaching of heavy metals from the aggregate samples was below the environmental limits within a pH range between 3 and 9. Subsequent washing of the leached aggregate with acidic CALWET solutions did not result in an additional release of heavy metals. It is proposed that coordinative bonding of the metal cations onto neutral surface sites and electrostatic adsorption led to stabilization of the heavy metals within the aggregate structure below hydrolysis pHs.
  • Article
    Citation - WoS: 41
    Citation - Scopus: 43
    Isomerisation of ?-Pinene Over Beta Zeolites Synthesised by Different Methods
    (Elsevier Ltd., 2005) Gündüz, Gönül; Dimitrova, Raina D.; Yılmaz, Selahattin; Dimitrov, Ljubomir; Spassova, Maya
    Liquid-phase α-pinene isomerisation at l00°C in a batch reactor is studied over Beta zeolites synthesised by different methods. It is confirmed that α-pinene forms a carbenium ion in an acidic environment, which rearranges without capture by nucleophiles, to form mainly hydrocarbons as camphene, terpinenes, terpinolenes and heavy products. The microporous Beta samples show low activity despite the high acidity most probably because of the hindered intermediate formation. The nature of the enhanced activity of Beta mesopores samples is suggested to be a result from the high accessibility of the acidic sites. The isomerisation of α-pinene was studied over Beta zeolites synthesised by different methods. The main products are camphene, terpinenes, terpinolenes and heavy products. Beta zeolites with micro-/mesopores reveal excellent activity because of the appropriate balance between acidity and bimodal pore system. The microporous Beta samples show low activity despite the good total acidity most probably because of the steric effect for the formation of the intermediate cations.