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921.
Solid circulation characteristics in an internally circulating fluidized bed with orifice-type draft tube 总被引:1,自引:0,他引:1
Sang Done Kim Yo Han Kim Seon Ah Roh Dong Hyun Lee 《Korean Journal of Chemical Engineering》2002,19(5):911-916
Effects of superficial gas velocities to a draft tube, to an annulus section and particle size on the solid circulation rate
(G,) have been determined in an internally circulating fluidized bed (0.28 m I.D. × 2m high) with an orifice type draft tube.
The solid circulation rate from the draft tube to an annulus section increases with increasing gas velocities to the draft
tube(U
d
) and annulus section (Ua) and consequent increase in pressure drop across the orifice (ΔPor). However, the values ofG
s
decrease by 7–21% with increasing particle size from 86 to 288 μm. The pressure drop across the orifice increases with increasingU
d
andU
a
. However, ΔPor decreases by 5–23% with increasing particle size. To predictG
s
in an internally circulating fluidized bed, a correlation is proposed as a function of ΔPor
This paper is dedicated to Professor Dong Sup Doh on the occasion of his retirement Korea University. 相似文献
922.
An axial dispersion of gas in a circulating fluidized bed was investigated in a fluidized bed of 4.0 cm I.D. and 279 cm in
height. The axial dispersion coefficient of gas was determined by the stimulus-response method of trace gas of CO2. The employed particles were 0.069 mm and 0.147 mm silica-sand. The results showed that axial dispersion coefficients were
increased with gas velocity and solid circulation rates as well as suspension density. The experimentally determined axial
dispersion coefficients in this study were in the range of 1.0-3.5 m2/s. 相似文献
923.
A CF3‐containing diamine, 4,4′‐bis(4‐amino‐2‐trifluoromethylphenoxy)benzophenone ( 2 ), was synthesized from 4,4′‐dihydroxybenzophenone and 2‐chloro‐5‐nitrobenzotrifluoride. Imide‐containing diacids ( 3 and 5Ba – 5Bg ) were prepared by the condensation reaction of aromatic diamines and trimellitic anhydride. Then, two series of novel soluble aromatic poly(amide imide)s (PAIs; 6Aa – 6Ak and 6Ba – 6Bg ) were synthesized from a diamine ( 4Aa – 4Ak or 2 ) with the imide‐containing diacids ( 3 and 5Ba – 5Bg ) via direct polycondensation with triphenyl phosphate and pyridine. The aromatic PAIs had inherent viscosities of 0.74–1.76 dL/g. All of the synthesized polymers showed excellent solubility in amide‐type solvents, such as N‐methyl‐2‐pyrrolidone and N,N‐dimethylacetamide (DMAc), and afforded transparent and tough films by DMAc solvent casting. These polymer films had tensile strengths of 90–113 MPa, elongations at break of 8–15%, and initial moduli of 2.0–2.9 GPa. The glass‐transition temperatures of the aromatic PAIs were in the range 242–279°C. They had 10% weight losses at temperatures above 500°C and showed excellent thermal stabilities. The 6B series exhibited less coloring and showed lower yellowness index values than the corresponding 6A series. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102:3641–3653, 2006 相似文献
924.
Jong-Ho Ryu Jong Hyun Seo Jae-Han Jeong Sung-Kap Kim Dong Nyung Lee 《Journal of Applied Electrochemistry》2004,34(9):879-884
A study has been made of the electrochemical etching of 99.99% aluminum foils at a current density of 50 mA cm–2in AlCl3–HCl solutions (1 m Cl–) at 80 °C. The solutions were made by dissolving metallic aluminum into 1m HCl solution, to give a Cl– concentration of 1 m. The number density of etch tunnels and the homogeneity of tunnel length decreased, and the mean pit size and its standard deviation increased with increasing Al3+ concentration. The results were discussed based on potential transients at a current density of 50 mA cm–2, current–potential curves at a scan rate of 10 m Vs–1 and electrochemical impedance spectra. 相似文献
925.
Sung‐Jun Cho 《应用聚合物科学杂志》2003,88(8):1904-1910
The polymerization of ?‐caprolactam between the interlamellar spaces of the [TEACOOH]–montmorillonite intercalations complex was attempted using Na–montmorillonite and 10‐carboxy‐n‐decyltriethylammonium bromide to achieve [TEACOOH]–polycaprolactam–montmorillonite, in which montmorillonite (inorganic polymer) is chemically bonded with the polycaprolactam (organic polymer). The results of X‐ray and IR analysis for the samples obtained after polymerization showed that the polymerization reaction has been successfully accomplished. For the purpose of studying the polymeric reaction product more precisely, we have isolated the polymerized product from the silicate layers and analyzed it with X‐ray diffractometer and IR spectrometer. Comparison of the results of X‐ray and IR analysis between the isolated polymer and the polymer that was synthesized by the reaction of ?‐caprolactam only with the organic cation without montmorillonite showed that both obtained polymers are the same compounds. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1904–1910, 2003 相似文献
926.
The thermal and thermomechanical properties of two series of poly(ethylene oxide) networks (NPEOs) were investigated as a function of the chain length between crosslink sites (Mc) and the concentration of LiClO4 (CL) in the NPEOs. The two series of networks were produced with silica and organic crosslinking agents and, therefore, had crosslink sites of different natures: one was an inorganic silicate network (silica NPEO), and the other was an organic polar group (organic NPEO). The crosslink sites in both series of networks were commonly covalently bonded to the poly(ethylene oxide) (PEO) phase through a urethane group in the NPEOs. The glass‐transition temperatures (Tg's) of the PEO phases in the NPEOs, according to differential scanning calorimetry, increased with a decrease in Mc and were higher in the silica NPEOs than in the organic NPEOs under the same Mc conditions. The difference in Tg between the two series of networks with the same Mc values increased with decreasing Mc. These results suggested that the interaction of crosslink sites with the PEO phase was stronger in the silica NPEOs than in the organic NPEOs. The addition of LiClO4 to the NPEOs resulted in Tg of the PEO phase in the NPEOs being elevated and increased according to the increase in CL. The increase of Tg of the PEO phase according to the increase of CL in the NPEOs was retarded or saturated at high values of CL, and this indicated that the limit of solubility of the salt in the polymer was attained. The retardation or saturation of the increase of Tg was also observed in dynamic mechanical analyses. The curves of the loss factor tan δ and temperatures from the dynamic mechanical analyses for the NPEOs with high values of CL showed shoulders or double peaks indicating the existence of the second phase in the polymer networks. In the curves of tan δ for salt‐complexed NPEOs with high values of CL, silica NPEOs showed a shoulder of low intensity, but organic NPEOs showed a distinguished second peak becoming stronger with increasing CL. The results of the Tg behavior and tan δ curves suggested that the salt solubility in the NPEOs was limited and that the salt solubility of PEO in the silica NPEOs was higher than that in the organic NPEOs. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 270–277, 2003 相似文献
927.
Won Seok Lyoo Han Do Ghim Hee‐Sam Kim Joon Ho Kim Sam Soo Kim Won Sik Yoon Jinwon Lee Sang‐Seob Lee 《应用聚合物科学杂志》2002,86(14):3667-3672
N‐Vinylcarbazole (VCZ) was solution‐polymerized in tetrahydrofuran (THF) at ?20, 0, and 20°C using the photoinitiation method; the effects of the amount of solvent, polymerization temperature, and photoinitiator concentration were investigated. On the whole, the experimental results corresponded to predicted ones. Low polymerization temperature using photoinitiation proved to be successful in obtaining poly(N‐vinylcarbazole) (PVCZ) of a high molecular weight with a smaller temperature rise during polymerization; nevertheless of free radical polymerization by 2,2′‐azobis(2,4‐dimethylvaleronitrile) (ADMVN). The photo‐solution polymerization rate of VCZ in THF was proportional to the 0.47 power of ADMVN concentration. The molecular weight was higher and the molecular weight distribution was narrower with PVCZ polymerized at lower temperatures. For PVCZ prepared in THF at ?20°C using a photoinitiator concentration of 0.00005 mol/mol of VCZ, a weight‐average molecular weight of 510,000 was obtained, with a polydispersity index of 1.73, and a degree of lightness converged to about 99%. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 3667–3672, 2002 相似文献
928.
Yun‐He Zhang Qin‐Hua Liu Ya‐Ming Niu Shu‐Ling Zhang Dong Wang Zhen‐Hua Jiang 《应用聚合物科学杂志》2005,97(4):1652-1658
A series of block copolymers composed of poly(ether ether ketone) (PEEK) and poly(ether ether ketone ketone) (PEEKK) components were prepared from their corresponding oligomers via a nucleophlilic aromatic substitution reaction. Various properties of the copolymers were investigated with differential scanning calorimetry (DSC) and a tensile testing machine. The results show that the copolymers exhibited no phase separation and that the relationship between the glass‐transition temperature (Tg) and the compositions of the copolymers approximately followed the formula Tg = Tg1X1 + Tg2X2, where Tg1 and Tg2 are the glass‐transition‐temperature values of PEEK and PEEKK, respectively, and X1 and X2 are the corresponding molar fractions of the PEEK and PEEKK segments in the copolymers, respectively. These copolymers showed good tensile properties. The crystallization kinetics of the copolymers were studied. The Avrami equation was used to describe the isothermal crystallization process. The nonisothermal crystallization was described by modified Avrami analysis by Jeziorny and by a combination of the Avrami and Ozawa equations. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1652–1658, 2005 相似文献
929.
LiNi1/3Co1/3Mn1/3O2 cathode materials have been coated with Al2O3 nano-particles using sol-gel processing to improve its electrochemical properties. The X-ray diffraction (XRD) pattern of the as-prepared Al2O3 nano-particles was indexed to the cubic structure of the γ-Al2O3 phase and had an average size of ∼4 nm. The XRD showed that the structure of LiNi1/3Co1/3Mn1/3O2 was not affected by the Al2O3 coating. However, the Al2O3 coatings on LiNi1/3Co1/3Mn1/3O2 improved the cyclic life performance and rate capability without decreasing its initial discharge capacity. These electrochemical properties were also compared with those of LiAlO2-coated LiNi1/3Co1/3Mn1/3O2 cathode material. The electrochemical impedance spectroscopy (EIS) was studied to understand the enhanced electrochemical properties of the Al2O3-coated LiNi1/3Co1/3Mn1/3O2 compared to uncoated LiNi1/3Co1/3Mn1/3O2. 相似文献
930.
This work was undertaken to discuss in depth the vital differences in the morphological development during synthesis, and properties of starch‐g‐poly‐(vinyl acetate) copolymers using two different initiators, potassium persulfate (KPS) and ceric ammonium nitrate (CAN). KPS‐initiated system gave relatively low values of grafting ratio and grafting efficiency, indicating a great tendency for the formation of poly(vinyl acetate) homopolymer (PVAc). Yet, higher values were seen for the CAN‐initiated system. Transmission electron microscope observations indicated a relatively broad distribution of latex particles for the KPS‐initiated system. The surface potential of latex particles was about ?3.5 mV, which turned out to be insufficient to maintain stability of latex particles. On the other hand, a uniform particle size distribution was found for the CAN‐initiated system, as the surface potential of latex particles was 21.5 mV. Moreover, radicals on starch molecules were generated directly through a redox reaction with positively charged ceric ion. The hydrophobic PVAc chains were thus grafted on starch, resulting in an amphiphilic graft copolymer, which provides a sufficient stabilization degree as a role of surfactant to render a relatively uniform distribution of latex particles. The synthesized starch‐g‐poly(vinyl acetate) copolymers were further converted to starch‐g‐poly(vinyl alcohol) through saponification, which were subjected to evaluations regarding the biodegradation and cell culture capability. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3017–3027, 2006 相似文献