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41.
This paper summarizes our research in the preparation of chain end functionalized isotactic polypropylene (PP) having a terminal functional group, such as Cl, OH, and NH2. The chemistry involves metallocene-mediated propylene polymerization using rac-Me2Si[2-Me-4-Ph(Ind)]2ZrCl2/MAO complex in the presence of styrene derivatives (St-f) and hydrogen, which serve as the chain transfer agents. The molecular weight of the resulting PP polymers with a terminal Cl, OH and NH2 group (i.e., PP-t-Cl, PP-t-OH and PP-t-NH2) are inversely proportional to the molar ratio of [St-f]/[propylene]. Despite the extremely low concentration of functional group, the high molecular weight chain end functionalized PP-t-OH and exhibit a distinctive advantage over other functional PP polymers containing side chain functional groups or long functional blocks. The terminal hydrophilic OH and cations, with good mobility and reactivity, effectively hydrogen bond and ion-exchange the cations (Li+, Na+, etc.) located between the clay interlayers, respectively. Such interactions anchor the PP chain to the clay surfaces. On the other hand, the remaining rest of the unperturbed end-tethered high molecular weight PP tail exfoliates the clay layers. This exfoliated structure is maintained even after further mixing of the PP-bearing platelets with pure neat PP polymers. 相似文献
42.
V. A. Drebushchak L. N. Mylnikova T. N. Drebushchak V. V. Boldyrev 《Journal of Thermal Analysis and Calorimetry》2005,82(3):617-626
Summary Ancient ceramic samples (single fragments and different parts of pots, unbroken and repaired; total about 180 samples) dated
from the transitional period of late Bronze to early Iron Age (VIII-VI centuries BC) and early Iron Age (VII-IV centuries
BC) were investigated by thermal analysis, X-ray powder diffraction, petrography, and scanning electron microscopy equipped
with the energy-dispersive X-ray analyzer. In addition to that, to identify the clay sources for the ceramic manufacturing,
about 15 samples of clays and soils found near archeological digs and taken from the mineralogical museum were investigated.
We found out that the calcite content of ceramics is a very informative parameter for the identification of the clay source
for the pottery manufactured at low technological level (low-temperature firing). 相似文献
43.
G. Rytwo R. Huterer-Harari S. Dultz Y. Gonen 《Journal of Thermal Analysis and Calorimetry》2006,84(1):225-231
Adsorption
of erythrosin-B (EB) and fast green (FG) to a non-charged organosmectite based
on crystal violet adsorbed up to 100% of the cation exchange capacity (CEC)
was tested. Adsorption isotherms of EB and FG were prepared at 3, 24 and 50°C.
All isotherms are of H-type reaching loads of approximately up to 20% of the
original CEC of the crude montmorillonite (up to 0.15 and 0.10 mol dye kg–1
clay for EB and FG, respectively). Adsorption decreases with temperature,
indicating an exothermic process. Enthalpy was evaluated using van’t
Hoff equation, yielding approximately –20 kJ mol–1
for both dyes. 相似文献
44.
J. Bujdák H. Slosiariková B. Číčel 《Journal of inclusion phenomena and macrocyclic chemistry》1992,13(4):321-327
Reduced charge montmorillonites (RCM) were prepared using lithium thermal treatment. The sorption of octylammonium (OA), dodecylammonium (DDA) and hexadecylammonium ions (HDA) on differently charged samples were studied. The amounts of DDA and HDA sorbed on each RCM exceed the cation exchange capacity (CEC) but that of OA exceeds only the CEC of samples with the lowest CEC. The sorption is affected not only by the layer charge but also by the formation of collapsed interlayer spaces in the lowest charged montmorillonites. X-ray measurements confirmed the decrease of the layer charge after lithium thermal treatment and the layer charge heterogeneity in RCMs. 相似文献
45.
Zr柱撑蒙脱土上负载稀土铈及铜铈催化剂的制备与表征 总被引:1,自引:0,他引:1
The Zr-pillaraed montmorillonite supported Ce and Cu-Ce catalysts were prepared by impregnation method. The performance of the catalysts was evaluated via the catalytic oxidation of volatile organic compounds (acetone, ethyl acetate, and toluene). The results showed that after supporting with Ce and Cu-Ce, the catalysts had a better reducibility. Moreover, the surface areas of the samples were increased. In addition,it was found that the Zr-pillared montmorillonite supported Cu-Ce catalysts had a higher activity and the reaction temperature decreased by 150~200 ℃ compared with the sample without Cu-Ce modification. 相似文献
46.
WANG Shufang SONG Cunjiang ** CHEN Guangxin LIU Jing YANG Chao ZHANG Xihui GUO Tianying ZHANG Banghua State Key Laboratory of Functional Polymer Materials for Adsorption Separation Institute of Polymer Chemistry N & T Joint Academy Nankai University Tianjin China Department of Microbiology Life Science College Nankai University Tianjin China 《Chinese Journal of Reactive Polymers》2004,(Z1)
1. INTRODUCTION Poly (3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) has been recognized as apotential environment-friendly substitute for traditional plastics. The structure, mechanicalproperties and biodegradability of PHBV as biodegradable plastic have been reported by many groups [1-3]. However, PHBV presents some problems, such as high cost, slow crystallization rate, relatively difficult processing and high degree of crystallinity. Therefore, it is difficult to use PHBV widel… 相似文献
47.
John M. Adams Keith Martin Richard W. McCabe 《Journal of inclusion phenomena and macrocyclic chemistry》1987,5(6):663-674
Suitably modified smectite clays can be very selective catalysts for a wide range of organic reactions. While it has long been known that such materials can act as Bronsted and Lewis acids, it has been shown recently that they are also effective Diels-Alder catalysts. A selection of illustrative reactions is given which emphasises their wide range of use, their selectivity, and the ease of work-up after reaction. In each case, mechanistic information is presented, e.g., on the site of reaction (whether interlayer or surface), rate determining steps, etc. The regiochemical consequences of the restricted reaction space are stressed.Based on material presented at the Fourth International Symposium on Inclusion Phenomena and the Third International Symposium on Cyclodextrins, Lancaster, U.K., 20–25 July 1986. 相似文献
48.
聚丙烯/纳米蒙脱土复合材料的结晶动力学研究 总被引:5,自引:1,他引:5
徐笑非 《分析测试技术与仪器》2002,8(1):26-30
采用热分析方法,研究了聚丙烯/纳米蒙脱土复合材料(PP/CLAY)的等温结晶行为,并分别用Avrami方程和赵志英方法对所得数据进行了分析,研究结果表明,纳米蒙脱土微粒对聚丙烯等温和非等温结晶行为均有不同程度的影响,可提高聚丙烯的结晶速率并改善结晶结构。 相似文献
49.
The reaction of trimethylbenzene (TMB) over alumina-pillared montmorillonite (Al-PM) had been investigated in a fixed-bed flow reactor at 300 °C and atmospheric pressure. Al-PM calcined in the range 300-500 °C exhibited decreased layer distance, surface area and acid amount. The strong acid sites of Al-PM calcined at 500 °C were greatly diminished according to measurements of ammonia temperature-programmed desorption. Under our conditions the reaction proceeded mainly via isomerization and disproportionation with little dealkylation. The conversion of reactant decreased in the order 1,2,3-TMB ≥ 1,2,4-TMB > 1,3,5-TMB and the selectivity of isomerization in the order 1,2,3-TMB > 1,3,5-TMB > 1,2,4-TMB, corresponding to the order of diminishing thermal instability. Both the catalytic activity and the selectivity ratio of disproportionation to isomerization decreased with increased calcined temperature and time-on-stream. o-Xylene content in the total xylene produced from 1,2,4-TMB or 1,2,3-TMB greatly exceeded the composition at thermodynamic equilibrium. These results arc consistent with the decrease of both the strong acid sites and the pore size of Al-PM which exhibits the restricted transition state selectivity. 相似文献
50.
Colloidal forces between bitumen surfaces in aqueous solutions measured with atomic force microscope
Jianjun Liu Zhenghe Xu Jacob Masliyah 《Colloids and surfaces. A, Physicochemical and engineering aspects》2005,260(1-3):217-228
Colloidal forces between bitumen surfaces in aqueous solutions were measured with an atomic force microscope (AFM). The results showed a significant impact of solution pH, salinity, calcium and montmorillonite clay addition on both long-range (non-contact) and adhesion (pull-off) forces. Weaker long-range repulsive forces were observed under conditions of lower solution pH, higher salinity and higher calcium concentration. Lower solution pH, salinity and calcium concentration resulted in a stronger adhesion forces. The addition of montmorillonite clays increased long-range repulsive forces and decreased adhesion forces, particularly when co-added with calcium ions. The measured force profiles were fitted with extended DLVO theory to show the repulsive electrostatic double layer and attractive hydrophobic forces being the dominant components in the long-range forces between the bitumen surfaces. At a very short separation distance (less than 4–6 nm), a strong repulsion of steric origin was observed. The findings provide a fundamental understanding of bitumen emulsion stability and a mechanism of bitumen “aeration” in bitumen recovery processes from oil sands. 相似文献