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An interactive computer program is introduced in order to make a simultaneous graphical presentation of phase boundaries and their corresponding free energy curves. The program, which uses a graphics display terminal, is a useful tool in teaching thermodynamic concepts involved in phase diagrams, especially for undergraduate students. 相似文献
85.
A new aromatic diamine monomer containing benzoxazole substituents was prepared by a multistep synthesis starting from 1,4‐dibromo‐2,5‐difluorobenzene. The diamine was polymerized with commercial aromatic dianhydride or dicarboxylic acid chloride monomers to provide several different poly(amic acid)s and polyamides with their inherent viscosities in the range of 0.24–0.46 dL/g. Thermal properties of these polymers including thermal imidization of poly(amic acid)s into polyimides were investigated by using FTIR, DSC, and TGA. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 178–185, 2004 相似文献
86.
A graft copolymer of 2-vinylnaphthalene (2-VN) and methyl methacrylate (MMA) onto ethylene–propylene–diene terpolymer (EPDM) was synthesized in tetrahydrofuran using benzoyl peroxide. The effects of EPDM content, and ratio of 2-VN to MMA, reaction time, reaction temperature, and initiator concentration in the graft copolymerization were examined. The light resistance, thermal stability, and the tensile properties of the graft copolymer were investigated by using Fade-o-Meter, thermogravimetric analyzer, and tensile tester. It was found that the light resitance and the heat resistance as well as the tensile strength of the graft copolymer are considerably better than those of the acrylonitrile–butadiene–styrene (ABS) copolymer. © 1994 John Wiley & Sons, Inc. 相似文献
87.
Intercalated nanocomposites with poly(butylene terephthalate) (PBT) incorporated between the montmorillonite layers were synthesized from dimethyl terephthalate and 1,4-butane diol by using an in situ interlayer polymerization. The PBT nanocomposites were melt-spun at different organoclay contents to produce monofilaments. The samples were characterized by using wide angle X-ray diffraction, electron microscopy, thermal analysis, and tensile testing. The extent of the clay layer in the PBT was confirmed by using X-ray diffraction and electron microscopy, and the clay layer was found to be highly dispersed on a nanometer scale. The addition of only a small amount of organoclay was enough to improve the thermo-mechanical properties of the PBT hybrid fibers. The hybrids were extruded with various draw ratios (DRs) to examine the tensile mechanical property of the fibers. At DR=1, the ultimate tensile strength of the hybrid fibers increased with the addition of clay up to a critical content and then decreased. However, the initial modulus monotonically increased with increasing amount of organoclay in the PBT matrix. When the DR was increased from 1 to 6, for example, the strength and the initial modulus values of the hybrids containing 3 wt% organoclay decreased linearly. 相似文献
88.
Pd catalysts supported on TiO2, ZrO2, ZSM-5, MCM-41 and activated carbon were used in catalytic wet oxidation of hydrocarbons such as phenol, m-cresol and m-xylene.
It was found that the Pd/TiO2 catalyst was highly effective in the wet oxidation of hydrocarbon. The activities of catalysts with various hydrocarbon species,
catalyst support, oxidation state of catalyst performed in a 3-phase slurry reactor show that reaction on Pd surface is more
favorable than that in aqueous phase and that the active site is oxidized Pd in catalytic wet air oxidation of hydrocarbons.
Based on the experimental results, a plausible reaction mechanism of wet oxidation of hydrocarbons catalyzed over Pd/TiO2 catalyst was proposed. This catalyst is superior to other oxide catalysts because it suppressed the formation of hardly-degradable
organic intermediates and polymer. 相似文献
89.
Pt, Ir, Pt-Ir and Pt-Ni bimetallic catalysts supported on NaY- and HY-zeolite were examined as a catalyst for producing gasoline
from n-decane via simultaneous reforming and cracking. The catalysts were prepared by calcining and reducing metal-ion-exchanged
Y-zeolite with O2 and H2 at 300°C., respectively. Thus prepared catalysts were characterized by hydrogen chemisorption and temperature programmed
desorption of ammonia. Pt-Ni/NaY and Pt-Ir/NaY bimetallic catalysts offered the improved activity maintenance compared to
Pt/NaY monometallic catalyst. The catalysts supported on HY-zeolite showed higher selectivity toward C5–C7 and skeletal isomers of C5–C7- and C8–C10 than those of the catalysts supported on NaY-zeolite, which is a desired characteristic for increasing octane value of gasoline
these days. However, deactivation with reaction time was much more pronounced on HY-zeolite-supported catalyst. When the catalyst
was prcsulfided with H,S, the stability with time on stream was enhanced and the selectivity was quite different from that
of the catalyst before presulfiding. The acidity of Y-zeolite and presulfiding of catalyst greatly influenced the activny,
selectivity and stability of Pt, Ir, Pt-Ir and Pt-Ni bimetallic catalysts supported on Y-zeolite in n-decane reforming reaction. 相似文献
90.
Alessandro Casnati Patrizia Minari Andrea Pochini Rocco Ungaro Wilma F. Nijenhuis Feike De Jong David N. Reinhoudt 《Israel journal of chemistry》1992,32(1):79-87
The p-tert-butylcalix[6]arene hexamide 2 and syn-1,3,5–trimethoxy-2,4,6-triamide 4 were synthesized by reaction of α-chloro-N,N-diethylacetamide and the corresponding calix[6]arenes 1 and 3 , respectively. 1H NMR spectroscopy shows that 2 is a mixture of different conformations whereas 4 is fixed in a cone conformation. Extraction experiments, (S-L) and (H2O–CDCl3) with picrate salts, indicate that 2 complexes both alkali metal (1:2 complex) and guanidinium salts (1:1 complex) but 4 complexes only guanidinium (1:1 complex). Incorporated in supported liquid membranes (Accurel® / o-nitrophenyl n-octyl ether) the calixarenes 2 and 4 transport guanidinium salts. The hexamide 2 is a more efficient carrier of guanidinium but the syn-1,3,5-trimethoxy-2,4,6-triamide 4 is much more selective. Both 2 and 4 are sufficiently lipophilic to give membranes that are stable over longer periods (weeks). 相似文献