TY - JOUR
T1 - Standardization of catalyst preparation using reference catalyst
T2 - Ion exchange of mordenite type zeolite, Remarkable dealumination accompanying ion exchange
AU - Katada, Naonobu
AU - Takeguchi, Tatsuya
AU - Suzuki, Tatsuya
AU - Fukushima, Toshihisa
AU - Inagaki, Kinya
AU - Tokunaga, Setsuo
AU - Shimada, Hiromichi
AU - Sato, Koichi
AU - Oumi, Yasunori
AU - Sano, Tsuneji
AU - Segawa, Kohichi
AU - Nakai, Kazuyuki
AU - Shoji, Hiroshi
AU - Wu, Peng
AU - Tatsumi, Takashi
AU - Komatsu, Takayuki
AU - Masuda, Takao
AU - Domen, Kazunari
AU - Yoda, Eisuke
AU - Kondo, Junko N.
AU - Okuhara, Toshio
AU - Kageyama, Yasuyoshi
AU - Niwa, Miki
AU - Ogura, Masaru
AU - Matsukata, Masahiko
AU - Kikuchi, Eiichi
AU - Okazaki, Noriyasu
AU - Takahashi, Motoi
AU - Tada, Akio
AU - Tawada, Shogo
AU - Kubota, Yoshihiro
AU - Sugi, Yoshihiro
AU - Higashio, Yasuhiko
AU - Kamada, Masahiko
AU - Kioka, Yukiyo
AU - Yamamoto, Kohei
AU - Shouji, Takayuki
AU - Arima, Yusaku
AU - Okamoto, Yasuaki
AU - Matsumoto, Hideyuki
PY - 2005/4/8
Y1 - 2005/4/8
N2 - A joint study was organized to establish a standard set of conditions for the ion exchange of zeolite from sodium into proton-form. The sodium-form mordenite with Si/Al2 = ca. 15 was ion exchanged into an NH4-form, followed by calcination according to various recipes. Then various advanced techniques for characterization (ICP, TG, XPS, SEM, XRD, N2 adsorption, 29Si and 27AlNMR, benzene diffusion, IR of OH and adsorbed pyridine and CO, ammonia TPD) were applied, and some test reactions (cracking of cumene, isopropylation of biphenyl, oligomerization of propene and chichibabin condensation of acetaldehyde and ammonia into picoline) were conducted. The ion exchange (removal of sodium) proceeded as expected, but remarkable differences were observed in physicochemical and catalytic properties of the thus-prepared proton-form samples. Exceptionally high temperature (383 K) for the ion exchange resulted in the structural degradation, while most samples exchanged at 333-353 K maintained the crystallinity and pore volume. The use of NH4Cl slightly changed the crystal morphology. Extra-framework aluminum species was formed on most samples after calcination above 773 K. In contrast, calcination at 673 K maintained the framework aluminum. Therefore, the dealumination is considered to proceed after complete removal of ammonia from the ammonium-form zeolite. However, the proton-form zeolite was stable under dry conditions, so it is speculated that the dealumination was induced by the contact of the proton-form zeolite to atmosphere with humidity. The total and Brønsted acidity decreased with the dealumination, while Lewis acidity increased. On the other hand, rapid heating of the ammonium type zeolite caused narrowing of the micropores. These structural changes seriously affected the catalytic activities for various reactions.
AB - A joint study was organized to establish a standard set of conditions for the ion exchange of zeolite from sodium into proton-form. The sodium-form mordenite with Si/Al2 = ca. 15 was ion exchanged into an NH4-form, followed by calcination according to various recipes. Then various advanced techniques for characterization (ICP, TG, XPS, SEM, XRD, N2 adsorption, 29Si and 27AlNMR, benzene diffusion, IR of OH and adsorbed pyridine and CO, ammonia TPD) were applied, and some test reactions (cracking of cumene, isopropylation of biphenyl, oligomerization of propene and chichibabin condensation of acetaldehyde and ammonia into picoline) were conducted. The ion exchange (removal of sodium) proceeded as expected, but remarkable differences were observed in physicochemical and catalytic properties of the thus-prepared proton-form samples. Exceptionally high temperature (383 K) for the ion exchange resulted in the structural degradation, while most samples exchanged at 333-353 K maintained the crystallinity and pore volume. The use of NH4Cl slightly changed the crystal morphology. Extra-framework aluminum species was formed on most samples after calcination above 773 K. In contrast, calcination at 673 K maintained the framework aluminum. Therefore, the dealumination is considered to proceed after complete removal of ammonia from the ammonium-form zeolite. However, the proton-form zeolite was stable under dry conditions, so it is speculated that the dealumination was induced by the contact of the proton-form zeolite to atmosphere with humidity. The total and Brønsted acidity decreased with the dealumination, while Lewis acidity increased. On the other hand, rapid heating of the ammonium type zeolite caused narrowing of the micropores. These structural changes seriously affected the catalytic activities for various reactions.
KW - Acidity
KW - Catalyst preparation
KW - Dealumination
KW - Ion exchange
KW - Mordenite
KW - Reference catalyst
KW - Standardization
KW - Zeolite
UR - http://www.scopus.com/inward/record.url?scp=14844298731&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=14844298731&partnerID=8YFLogxK
U2 - 10.1016/j.apcata.2004.12.036
DO - 10.1016/j.apcata.2004.12.036
M3 - Article
AN - SCOPUS:14844298731
SN - 0926-860X
VL - 283
SP - 63
EP - 74
JO - Applied Catalysis A: General
JF - Applied Catalysis A: General
IS - 1-2
ER -