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121.
Zhang De-Qing Wang Shao-Jun Sun Hong-Shan Wang Xiu-Li Cao Mao-Sheng 《Journal of Sol-Gel Science and Technology》2007,41(2):157-161
Lead zirconate titanate nanopowders Pb(Zr0.52Ti0.48)O3 (PZT) were prepared by modified sol-gel process in ethylene glycol system with zirconium nitrate as the zirconium source.
The research showed that it was critical to add lead acetate after the reaction of zirconium nitrate and tetrabutyl titanate
in ethylene glycol system for preparing PZT of exact titanium content. The reaction mechanisms of the sol synthesis, preparation
of xerogel and agglutinating process were characterized through using FT-IR, NMR, TG-FTIR, and GC-MS. The experiment proved
that ethylene glycol system did not rely on hydrolysis and condensation reactions in the process of the sol formation, but
on the formation of chain or network large molecules from complexation of ethylene glycol and all Ti and minor Pd, Zr. In
the preparation of xerogel, the complexation reaction was so completed that it formed large molecules network composed of
metal and dioxyethyl. Bulk weight loss happened before 350°C in the process of sintering xerogel to prepare PZT nanopowders.
Volatile matters and vapor phase decomposition resultants were primarily oxy-compounds including ethylene glycol, aldehyde-ketone
compounds, carbon dioxide and nitrate radical conversion matters. After 350°C, primary vapor phase decomposition resultants
were carbon dioxide and minor carbonyl compound. 相似文献
122.
Silica gel impregnated with poly(ethylene glycol) of different molecular mass (400, 1000, 1540, 4000, and 5500) was investigated for salting-out thin-layer chromatography of 15 mixed aminocarboxylato Co(III) complexes using eight ammonium sulphate solutions as mobile phases. Regularities established earlier for non-impregnated adsorbents are also valid in this work. Poly(ethylene glycol) of high molecular mass increases the hydrophobicity of the adsorbent. Positive linear dependence of RM values and of salting-out efficiency on average poly(ethylene glycol) molecular mass was usually observed. In contrast with non-impregnated silica gel, separation was achieved between complexes with the smallest hydrocarbon groups. 相似文献
123.
124.
Using infrared reflection absorption spectroscopy (IRRAS), quartz crystal microbalance (QMB) measurements, and X-ray photoelectron spectroscopy (XPS) in combination with chemical derivatization techniques the VUV photolysis of polyethylene (PE), polypropylene (PP), and polystyrene (PS) was investigated. A mass balance obtained from the quantification of the data was used to suggest reaction path ways. Although PE and PP behave similar, the mass loss is about 8 times higher in the case of PP. These differences originate from the higher disproportionation to recombination ratio for the branched polymer. Both polymers form double bonds and at extended treatment times they tend to crosslink. PS is rather stable due to the possibility of the energy dissipation by fluorescence. 相似文献
125.
Diblock copolymers composed of poly(oxy-ethylene) (POE) and poly(dl-lactic acid) segments were synthesized by anionic polymerization of d,l-lactide using the oxyanion formed by reaction of the monohydroxyl monomethoxy-poly(ethylene glycol) on sodium hydride. For comparison, a similar copolymer was prepared by using tin octoate to catalyze the lactide polymerization. The copolymers were used to make nanoparticles, which were stored at 4 °C. After a few months under these storage conditions, a dramatic decrease of the poly(ethylene glycol) content was observed, however, the mean diameter of the nanoparticles was not affected. The degradation of the nanoparticles was investigated in vitro under conditions selected to mimic physiological conditions. Changes of characteristics were monitored by 1H NMR, SEC, DLLS and CZE on nanoparticles and/or on the degradation by-products dissolved in the ageing medium. According to their nanometric dimensions, the microparticles degraded very slowly and there was no difference in behaviour between the sodium hydride and the stannous octoate-derived copolymers. 相似文献
126.
M. M. R. Talukder M. M. Zaman Y. Hayashi J. C. Wu T. Kawanishi 《Applied biochemistry and biotechnology》2007,141(1):77-83
The thermostability of Cromobacterium viscosum lip ase (EC 3.1.1.3) entrapped in AOT (sodium bis-[2-ethylhexyl] sulfosuccinate) reverse micelles was in creased by the addition
of short-chain polyethylene glycol (PEG 400). Two different approaches were considered: (1) the determination of half-life
time and (2) the mechanistic analysis of deactivation kinetics. The half-life of lipase entrapped in AOT/isooctane reverse
micelles with PEG 400 at 60°C was 28h, ninefold higher than that in reverse micelles without PEG 400. The lip ase entrapped
in both reverse micellar systems followed a series-type deactivation mechanism involving two first-order steps. The deactivation
constant for the first step at 60°C in PEG containing reverse micelles was 0.055 h11, 11-fold lower than that in reverse micelles without PEG, whereas it remained almost constant for the second step. The inactivation
energy of the lip ase entrapped in reverse micelles with and without PEG 400 was 88.12 and 21.97 kJ/mol, respectively. 相似文献
127.
G. Dlubek J. Stejny Th. Lüpke D. Bamford K. Petters Ch. Hübner M. A. Alam M. J. Hill 《Journal of Polymer Science.Polymer Physics》2002,40(1):65-81
High‐quality positron lifetime measurements (70 million total counts) are reported for polyethylenes (PEs) of different crystallinities (Xc = 3–82%). The specific volumes of the crystalline and amorphous phases (Vc and Va, respectively) were estimated from density and wide‐angle X‐ray scattering (WAXS) experiments. Some samples (those with low values of Xc) were branched PEs, and those with high values of Xc were linear PEs for which Xc was varied with changes in the crystallization temperature. Both Vc and Va increase with decreasing Xc in the range 0% ≤ Xc ≤ 56% (the branched PEs) but are constant for Xc ≥ 56% (the linear PEs). The lifetime spectra were analyzed with the MELT and LIFSPECFIT routines. Artifacts that can appear in the spectrum analysis were checked via an analysis of computer‐generated spectra. Four lifetime components appeared in all of the PEs; the two long‐lived ones are attributed to pick‐off annihilation of ortho‐positronium (o‐Ps) in crystalline regions (τ3) and in holes of the amorphous phase (τ4). With increasing Xc, τ3 decreases from about 1.2 to 1 ns, τ4 decreases from 3.0 to 2.5 ns, and the intensity I4 decreases from 29 to 0%. An increase in I3 from 6 to 12% was observed. A comparison with simulations shows that the true I3 value approaches 0 for Xc → 0%. The decrease in I4 is weaker than the increase in Xc; this leads to the conclusion that the apparent specific o‐Ps yield in the amorphous phase I4Xc increases with Xc. Possible reasons for this surprising results are discussed. The fractional free hole volume [h = (Va ? Vocc)/Va, where Vocc is the crystalline occupied volume] was estimated from density and WAXS results. Between Xc = 0 and 56%, h decreases from 0.151 to 0.090, but it does not change further above Xc = 56%. The mean size (v) of the local free volumes (holes) estimated from τ4 decreases from 200 to 150 Å3. The number density of holes (Nh) calculated from these values (Nh = h/v) also decreases from 0.8 to 0.6 nm?3 in the range 0% ≤ Xc ≤ 56%. The values of Va, Vc, h, and Nh increase with an increasing degree of branching but do not vary for linear PEs. The possible influence of a crystalline–amorphous interfacial phase (three‐phase model) on the observed lifetime parameters is also discussed. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 40: 65–81, 2002 相似文献
128.
Mingbi Qi Fengying Yao Jun Zheng Renyuan Qian 《Journal of Thermal Analysis and Calorimetry》1993,40(2):783-789
In this paper two LLDPE samples with their own structural parameters were studied by means of DSC. Experimental results show
that DSC was good for revealing slight structural difference between these two samples. Furthermore, the effect of thermal
history on crystallization and melting behaviour of LLDPE was observed clearly through varying conditions of thermal treatment.
Zusammenfassung Mittels DSC werden zwei LLDPE-Proben mit ihren eigenen Strukturparametern untersucht. Die Versuchsergebnisse zeigen, da\ sich DSC gut eignet, um gering fügige Unterschiede dieser zwei Proben nachzuweisen. Weiterhin wurde unter verschiedenen Bedingungen der Einflu\ der thermischen Vorgeschichte auf das Kristallisations-und Schmelzverhalten von LLDPE untersucht.相似文献
129.
L. Hernandez M. Rudolph R. Lammertink J. Kornfield C. Zurita F. A. Gomez 《Chromatographia》2007,65(5-6):299-303
Vancomycin (Van) from Streptomyces orientalis has been derivatized with polyethylene glycol [PEG; PEG-550 (1), 750 (2), 1,100 (3), 2,000 (4), 5,000 (5), and 8,000 (6) g mol−1] at the N-terminus of the glycopeptide backbone and their binding to d-Ala-d-Ala terminus peptides assessed using affinity capillary electrophoresis (ACE). Utilizing ACE, a plug of Van-PEG and non-interacting
standards are injected and electrophoresed. Analysis of the change in the relative migration time ratio of the Van-PEG species,
relative to the non-interacting standards, as a function of the concentration of peptide, yields a value for the binding constant
(K
b). Values of K
b for N-acetyl-d-Ala-d-Ala, 7 to the Van-PEG derivatives are weaker than those for N
α,N
ε-diacetyl-Lys-d-Ala-d-Ala, 8 (for example, values of K
b for 7-1 and 8-1 are 1.8 and 47.7 × 103 M−1, respectively). These results demonstrate that derivatization of Van with PEG has little effect on the affinity of d-Ala-d-Ala peptide ligands to it. The findings further prove the versatility of ACE and its ability to estimate binding parameters
of ligands to antibiotics. 相似文献
130.