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51.
Hyun-Seob?Song Joo?Sung?Lee Jae?Chun?HyunEmail author 《Korean Journal of Chemical Engineering》2002,19(6):949-953
A mathematical model for the pyrolysis reaction of polystyrene (PS) in a semi-batch reactor has been presented. The thermal
degradation of PS was flexibly modeled by a combination of random and specific chain-end scissions. Numerical simulation was
used to investigate the effect of operating conditions on the PS products spectrum, the results of which were validated by
the experimental data. It was found that as the reaction temperature increased (decreased), the monomer fraction in the products
became lower (higher) while the trimer higher (lower). No significant variation in the product composition was, however, observed
while constant temperature was maintained. These results indicate the reaction temperature is an effective manipulated variable
for the control of products composition of PS pyrolysis. The calculation of the optimum temperature trajectories through the
optimization study can thus be of interest for achieving productivity enhancement in plastics pyrolysis processes.
This paper is dedicated to Professor Dong Sup Doh on the occasion of his retirement from Korea University. 相似文献
52.
Various dynamical characters of continuous stirred tank reaclors (CSTR) are introduced with respect to the effects of reaction
types, extra thermal capacitance, periodic forcing, and coupling of CSTRs. The subject includes the classical dynamics of
two-dimensional model and the variety of complex dynamics in three or higher dimensional systems such as periodic bifurcations
to torus or chaos, aperiodic oscillations on invariant torus, and universal dynamics of alternating periodic-chaotic sequences
with k.2v-cycles for every natural number k. Particularly this review intends to bring about the problems that the engineers must be
prepared to encounter in solving various physical systems including chemically reacting systems. 相似文献
53.
Highly Efficient Overall Water Splitting Through Optimization of Preparation and Operation Conditions of Layered Perovskite Photocatalysts 总被引:1,自引:0,他引:1
Jindo Kim Dong Won Hwang Hyun Gyu Kim Sang Won Bae Jae Sung Lee Wei Li Se Hyuk Oh 《Topics in Catalysis》2005,35(3-4):295-303
The layered perovskite materials were found to give the high photocatalytic activity in water splitting reaction under UV
irradiation, where the electronic structure of perovskite slab constructing the layered structure (the total cation valency)
was the most crucial factor to the high photocatalytic activity. Both the excessive cation valency and the layered structure
were required for active photocatalysts, while the slab thickness of layered perovskites had an insignificant effect on water-splitting
activity. In order to identify key variables that affected photocatalytic activity and to optimize the performance of (110)
layered perovskite, La2Ti2O7 was modified by various methods. The optimum amount of loaded nickel had a great effect and the amount depended on the surface
area of the perovskite phase. When an alkaline-earth element such as Ba, Sr, and Ca was doped on La2Ti2O7, the photocatalytic activity was enhanced markedly. Introduction of an alkaline hydroxide into the reaction system as an
external additive enhanced the activity further showing extremely high quantum yields close to 50%. 相似文献
54.
High oleic acid oil suppresses lung tumorigenesis in mice through the modulation of extracellular signal-regulated kinase cascade 总被引:2,自引:0,他引:2
Yamaki T Yano T Satoh H Endo T Matsuyama C Kumagai H Miyahara M Sakurai H Pokorny J Shin SJ Hagiwara K 《Lipids》2002,37(8):783-788
This study was undertaken to estimate the effect of dietary high oleic acid oil (OA) on 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone
(NNK)-induced lung tumorigenesis in mice. Diet containing 10% oil was fed to mice through experimental periods. On day 30
after NNK injection (100 mg/kg body weight, i.p.), the treatment increased the level of prostaglandin E2 (PGE2) as well as proliferating cell nuclear antigen, a marker of cell proliferation in a high linoleic acid oil (LA)-fed group
but not in an OA-fed group. The NNK treatment also induced the activation of an extracellular signal-regulated kinase (Erk)
cascade (Erk, Mek and Raf-1) in an LA-fed group. On the other hand, OA feeding abolished the NNK-induced activation of the
Erk cascade. In conjugation with these events, OA feeding reduced lung tumor incidence and tumor multiplicity (percentage
of mice with tumors) in mice compared with LA feeding at the 20th experimental week. These results suggest that OA suppresses
lung tumorigenesis and that this suppression is correlated with the inhibition of PGE2 production and inactivation of the Erk cascade. 相似文献
55.
The sintering and electrical characteristics of La-modified Na1/2 Bi1/2 TiO3 (NBT) was investigated from a defect structure viewpoint. To reveal the role of cation vacancies, two series of ceramics, with different cation vacancies, were processed to compensate the excess positive charge of lanthanum ions. In a region of complete solid solution, the grain size of NBLT-B {[(Na0.5 Bi0.5 )1− x La x ]Ti1−0.25 x O3 } was smaller than that of NBLT-A {[(Na0.5 Bi0.5 )1−1.5 x La x ]TiO3 } and densification was enhanced more effectively in NBLT-B. With the aid of thermoelectric power, electric conductivity, and electrotransport measurements, it was found that different sintering behaviors between NBLT-A and NBLT-B specimens were related to the change in the type of cation vacancies present and that lanthanum ion–cation vacancy pairs played an important role in reducing the grain growth and enhancing the densification process. 相似文献
56.
Depolymerization of the biopolymer chitosan by an autoclaving process at 121°C and 15 psi was investigated using various treatments. Acetic acid was found to be the most effective solvent in decreasing chitosan viscosity among the six organic acids tested. The rate of viscosity decrease increased with increasing chitosan concentration. The viscosity of 1% chitosan in 1% acetic acid decreased rapidly to 91% of the initial viscosity following the initial 15 min of autoclaving. This decreased gradually to 93% and 94% in 30 and 60 min, respectively, without being adversely affected by the chitosan solution volume. The degree of deacetylation was comparable before and after autoclaving for 60 min. Chitosan at three molecular weights (Mr = 1597, 1110, and 789 kDa) decreased in molecular weight by 46%–51% in the 15‐min treatment, 55%–60% in the 30‐min treatment, and 60%–62% in the 60‐min treatment. The addition of 0.1%–1.0% (v/v) concentrations of hydrogen peroxide to the chitosan solution autoclaved for 15 min decreased viscosity by 94%–98% and molecular weight by 69%–83%. This process is a simple, timesaving, homogeneous depolymerization procedure, and it is possible to prepare partially hydrolyzed chitosan with specified molecular weights by regulating the time of treatment. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1890–1894, 2003 相似文献
57.
Polyvinylpyrrolidone (PVP)/sodium montmorillonite (MMT) nanocomposites prepared via the solution intercalation method were investigated by UV/vis, SEM, X-ray diffraction, TEM, FT-IR and PLM (polarized light microscopy). PVP/MMT nanocomposites show exfoliation below 20 wt% MMT and intercalation above this concentration. Nanocomposites retain good optical clarity and increased thermal resistance with MMT content. The compatibility between PVP and MMT and their enhanced properties may be explained by hydrogen bonding interactions. In addition, the nanocomposites prepared under more rigorous mixing conditions show better transparency because the smaller particle sizes are induced. In addition, the study on optically clear PVP/MMT suspensions helps one to understand how optical anisotropy of MMT is affected by the existence of polymer in aqueous solution. 相似文献
58.
Han Mo Jeong Shang Hoon Lee Kwang Jae Cho Young Tae Jeong Kap Ku Kang Jae Kwon Oh 《应用聚合物科学杂志》2002,84(9):1709-1715
The block copolymer of poly(1‐hexadecene) (PHD) and polypropylene (PP) was effectively synthesized by the sequential polymerization of propylene and 1‐hexadecene by using highly isospecific TiCl3/Cp2Ti(CH3)2 (Cp = cyclopentadienyl). The block copolymers had two separate melting temperatures of constituent blocks. The modulus of PHD–PP block copolymer was enhanced as the content of sequentially polymerized PP block was increased. The elongation at break showed positive deviation at the intermediate compositions from the simple additive values of constituent homopolymers. Shape memory effect which utilizes the crystalline PHD block as a reversible phase and the crystalline PP block as a fixed structure was examined. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1709–1715, 2002; DOI 10.1002/app.10551 相似文献
59.
Changyong Choi Su Young Chae Tai‐Hyoung Kim Jung Keon Kweon Chong Su Cho Mi‐Kyeong Jang Jae‐Woon Nah 《应用聚合物科学杂志》2006,99(6):3520-3527
Diblock copolymers with different poly(ε‐caprolactone) (PCL) block lengths were synthesized by ring‐opening polymerization of ε‐caprolactone in the presence of monomethoxy poly(ethylene glycol) (mPEG‐OH, MW 2000) as initiator. The self‐aggregation behaviors and microscopic characteristics of the diblock copolymer self‐aggregates, prepared by the diafiltration method, were investigated by using 1H NMR, dynamic light scattering (DLS), and fluorescence spectroscopy. The PEG–PCL block copolymers formed the self‐aggregate in an aqueous environment by intra‐ and/or intermolecular association between hydrophobic PCL chains. The critical aggregation concentrations of the block copolymer self‐aggregate became lower with increasing hydrophobic PCL block length. On the other hand, reverse trends of mean hydrodynamic diameters were measured by DLS owing to the increasing bulkiness of the hydrophobic chains and hydrophobic interaction between the PCL microdomains. The partition equilibrium constants (Kv) of pyrene, measured by fluorescence spectroscopy, revealed that the inner core hydrophobicity of the nanoparticles increased with increasing PCL chain length. The aggregation number of PCL chain per one hydrophobic microdomain, investigated by the fluorescence quenching method using cetylpyridinium chloride as a quencher, revealed that 4–20 block copolymer chains were needed to form a hydrophobic microdomain, depending on PCL block length. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3520–3527, 2006 相似文献
60.