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991.
Young-Kwon Park Hyung Won Lee Jong-Ki Jeon Seung-Soo Kim Changkook Ryu Ji Man Kim Ho-Jeong Chae Kwang-Eun Jeong 《Research on Chemical Intermediates》2011,37(9):1283-1291
The catalytic cracking of oil fractions separated from summer food waste leachate was investigated over BEA zeolite and Al-SBA-15 catalysts. In this study, a mixture of food waste oil fractions and catalyst was directly introduced to pyrolysis gas chromatography/mass spectrometry (Py-GC/MS), with the resulting vapor phase products being simultaneously analyzed. Various acid compounds, including oleic acid, produced by the non-catalytic pyrolysis of food waste leachate were reformed into valuable compounds, such as oxygenates, hydrocarbons, and aromatics. The BEA zeolite catalyst showed higher selectivity for hydrocarbon compounds, especially aromatics, within the gasoline range due to its superior cracking ability originating from its highly acidic sites. Conversely, the cracking performance of the Al-SBA-15 catalyst, possessing mild acidic sites, was lower than that of the BEA zeolite. Increasing the amount of Al-SBA-15 catalyst enhanced the cracking activity and resulted in higher selectivity for hydrocarbons. 相似文献
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994.
Nicholas Kob Russell S. Drago Vaneica Young John Osegovic 《Reaction Kinetics and Catalysis Letters》1999,66(2):205-210
The regeneration of solid acid catalysts used in alkylation was studied using cal-ad. It was found that an acid site strength
of −ΔH=32 kcal/mol is needed to catalyze the reaction. 相似文献
995.
Jeong‐Heui Choi Hae‐Jung Yoon Jung‐Ah Do Yong‐Chun Park Jae Hun Kim Dongmi Choi 《Biomedical chromatography : BMC》2011,25(4):493-497
A residual determination method as a regulatory residue method was developed using HPLC‐UVD for prohexadione residues in Chinese cabbage (Brassica pekinensis) and apple (Malus domestica). The developed method consisted of solid–liquid extraction with acidic acetonitrile and ion‐suppression liquid–liquid partitioning, followed by anion exchange cartridge cleanup. The limits of detection and quantitation for the method were 0.005 and 0.02 mg/kg, respectively. The method gave good linearity in the range of 0.02–2.5 mg/kg. Accuracy and precision ranged from 84.1 to 94.1% and from 2.4 to 6.9%, respectively. Additionally, the confirmative conditions of LC‐MS/MS for prohexadione were set in negative electrospray ionization mode with transitions of m/z 211.4 → 167.5 and m/z 211.4 → 123.5 in the selected reaction monitoring mode. The applicability of the method was demonstrated by analyzing real samples collected from local markets in Seoul, Republic of Korea. This developed method fully deserves consideration in accordance with its sensitivity, accuracy and precision required for residue analysis of prohexadione in Chinese cabbages and apples. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
996.
Seong-Ho Kim Yong-Kyun Sim Bum-Tae Kim Yong Hwan Kim Yeong-Joon Kim Seongsoon Park Hyuk Lee 《Tetrahedron: Asymmetry》2011,22(14-15):1499-1504
A synthetic method for lactic acid oligomers via solid-phase synthesis under mild reaction conditions with up to 99% yield is presented. The fine control of the chirality on each lactic acid unit of the oligomers was easily achieved by the substitution of (R)-THP-protected lactic acid (R)-2 by (S)-2 without alternating the procedure. The overall synthesis of the trimer and tetramer was completed in one and two days, respectively. Intramolecular cyclizations of enantio-controlled lactic acids were also attempted through the Yamaguchi macrolactonization or the Mitsunobu reaction. However, we were unable to isolate single cyclic oligomers but always obtained a mixture of cyclic oligomers. 相似文献
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999.
Jung-Kyen Moon Jung-Won Park Woo Song Lee Young-Jin Kang Hyun-A Chung Mi-Seon Shin Yong-Jin Yoon Ki Hun Park 《Journal of heterocyclic chemistry》1999,36(3):793-798
This paper presents the synthesis of 2-amino-, 2-acetamido- and 2-benzamidothioxanthones and their 10,10-dioxides. 相似文献
1000.