催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2010年
2期
236-241
,共6页
徐俊峰%刘坚%赵震%张桂臻%段爱军%姜桂元%徐春明
徐俊峰%劉堅%趙震%張桂臻%段愛軍%薑桂元%徐春明
서준봉%류견%조진%장계진%단애군%강계원%서춘명
三维有序大孔材料%钙钛矿氧化物催化剂%胶体晶体模板%柴油机炭黑颗粒%催化燃烧
三維有序大孔材料%鈣鈦礦氧化物催化劑%膠體晶體模闆%柴油機炭黑顆粒%催化燃燒
삼유유서대공재료%개태광양화물최화제%효체정체모판%시유궤탄흑과립%최화연소
three-dimensionally ordered macroporous material%perovskite-type oxide catalyst%colloid crystal template%diesel soot%catalytic combustion
采用水油两相双引发剂的无皂乳液聚合法制备了羧基改性的聚甲幕丙烯酸甲酯(PMMA)聚合物微球,并以此为模扳,采用胶体晶体模板法制备了三维有序大孔(3DOM)钙钛矿LaFeO_3催化剂.同时采用柠檬酸络合燃烧法制备了纳米钙钛矿LaFeO_3催化剂.通过傅里叶红外光谱、扫描电镜、X射线衍射和激光粒度仪等方法对样品进行了表征.采用程序升温氧化反应评价了催化剂对模拟柴油机炭黑颗粒催化燃烧的活性.结果表明,制备的羧基改性PMMA聚合物微球固含量约为10%,表面羧基含量约为3mmol/g.微球粒径分布均匀,且可通过调节反应条件得到不同的粒径,町控范围在300~700nm.所制得的3DOM钙钛矿LaFeO_3催化剂以六方有序的方式排列,其孔径及孔径收缩率分别为300nm和32%,大孔孔壁甲均厚度约50nm.该催化剂对炭黑颗粒催化燃烧的T_(10),T_(50),T_(90)和S~m_(CO2)分别为340,412,458℃和99.8%,件能优于纳米LaFeO_3催化剂.
採用水油兩相雙引髮劑的無皂乳液聚閤法製備瞭羧基改性的聚甲幕丙烯痠甲酯(PMMA)聚閤物微毬,併以此為模扳,採用膠體晶體模闆法製備瞭三維有序大孔(3DOM)鈣鈦礦LaFeO_3催化劑.同時採用檸檬痠絡閤燃燒法製備瞭納米鈣鈦礦LaFeO_3催化劑.通過傅裏葉紅外光譜、掃描電鏡、X射線衍射和激光粒度儀等方法對樣品進行瞭錶徵.採用程序升溫氧化反應評價瞭催化劑對模擬柴油機炭黑顆粒催化燃燒的活性.結果錶明,製備的羧基改性PMMA聚閤物微毬固含量約為10%,錶麵羧基含量約為3mmol/g.微毬粒徑分佈均勻,且可通過調節反應條件得到不同的粒徑,町控範圍在300~700nm.所製得的3DOM鈣鈦礦LaFeO_3催化劑以六方有序的方式排列,其孔徑及孔徑收縮率分彆為300nm和32%,大孔孔壁甲均厚度約50nm.該催化劑對炭黑顆粒催化燃燒的T_(10),T_(50),T_(90)和S~m_(CO2)分彆為340,412,458℃和99.8%,件能優于納米LaFeO_3催化劑.
채용수유량상쌍인발제적무조유액취합법제비료최기개성적취갑막병희산갑지(PMMA)취합물미구,병이차위모반,채용효체정체모판법제비료삼유유서대공(3DOM)개태광LaFeO_3최화제.동시채용저몽산락합연소법제비료납미개태광LaFeO_3최화제.통과부리협홍외광보、소묘전경、X사선연사화격광립도의등방법대양품진행료표정.채용정서승온양화반응평개료최화제대모의시유궤탄흑과립최화연소적활성.결과표명,제비적최기개성PMMA취합물미구고함량약위10%,표면최기함량약위3mmol/g.미구립경분포균균,차가통과조절반응조건득도불동적립경,정공범위재300~700nm.소제득적3DOM개태광LaFeO_3최화제이륙방유서적방식배렬,기공경급공경수축솔분별위300nm화32%,대공공벽갑균후도약50nm.해최화제대탄흑과립최화연소적T_(10),T_(50),T_(90)화S~m_(CO2)분별위340,412,458℃화99.8%,건능우우납미LaFeO_3최화제.
Carboxy-modified polymethyl methacrylate (PMMA) microspheres were prepared using an emulsifier-free emulsion polymeriza-tion technique with water-oil biphase double initiators. Three-dimensionally ordered macroporous (3DOM) LaFeO_3 perovskite-type complex oxide was synthesized using a colloid crystal template, which was assembled by centrifugation of carboxy-modified PMMA spheres. The nanometric LaFeO_3 oxide as a reference sample was also prepared by the citric acid ligation method. The samples were characterized by the techniques of Fourier transform infrared spectroscopy, scanning electron microscopy, X-ray diffraction, and a laser particle size analyzer. Their catalytic performance for diesel soot combustion was investigated by temperature-programmed oxidation reaction. The results indi-cated that the obtained carboxy-modified PMMA spheres had carboxyl groups on the surface and did not show any aggregation, and they were suitable for the preparation of colloidal crystals. Their contents of solids and carboxyl groups were 10% and 3 mmol/g, respectively. The particle size distribution of the microspheres was narrow and the microspheres with diameter of 300-700 nm can be designed and pre-pared under different process conditions. The obtained 3DOM LaFeO_3 catalyst had a hexagonally well-ordered array, and the diameter of macropore was about 300 nm, corresponding to a shrinkage ratio of 32%. The average thickness of its hole wall was about 50 nm. The T_(10), T_(50), T_(90), and S_(CO2)~m of 3DOM LaFeO_3 catalyst for soot combustion were 340, 412, 458 ℃ and 99.8%, respectively. Compared with the nano-LaFeO_3 catalyst for soot combustion, 3DOM LaFeO_3 catalyst has higher activity.