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排序方式: 共有63条查询结果,搜索用时 15 毫秒
1.
Jumiarti Agus Hideki Abe Yoshiharu Doi Takeharu Tsuge 《Polymer Degradation and Stability》2006,91(8):1645-1650
Polyhydroxyalkanoate (PHA) synthase (PhaC) from Wautersia eutropha was expressed in a wide range of production level in Escherichia coli XL1-Blue cells and its effects on PhaC activity, poly[(R)-3-hydroxybutyrate] [P(3HB)] production and its molecular weights were investigated. The production level of PhaC was controlled both by the amount of chemical inducer (isopropyl-β-d-thiogalactopyranoside, IPTG) added into the medium and the use of different copy number of plasmids. In a flask experiment, as PhaC production level in the cells increased, the PhaC activity also increased in the range of low PhaC concentration. However, PhaC activity did not further increase in the range of high PhaC concentration, probably due to the formation of inclusion body in the cells. The molecular weight of P(3HB) was found to decrease with increasing PhaC activity. This trend was also verified in high cell density cultivation using 10-l jar fermentor. Furthermore, we demonstrated that the use of low copy number plasmid and appropriate induction of PhaC expression were effective in achieving both high productivity and high molecular weight of P(3HB). 相似文献
2.
Alexander Semenov Aurélia Charlot Rachel Auzély-Velty Marguerite Rinaudo 《Rheologica Acta》2007,46(5):541-568
Dynamics of associating polymer solutions above the reversible gelation point are studied. Each macromolecule consists of
a soluble backbone (B) and a small fraction of specific strongly interacting groups (A or C stickers) attached to B. A mixture
of B–A and B–C associating polymers with 1:1 stoichiometric ratio is considered. As a result of AC association, the polymers
reversibly gelate above the overlap concentration. It is shown that (1) the network strands are linear complexes (double chains)
of B–A and B–C; (2) “diffusion” of the network junction points is characterized by an apparent activation energy, which can
be significantly higher than the energy of one AC bond; (3) most importantly, the randomness of sticker distribution along
the chain can significantly slow down the network relaxation leading to a markedly non-Maxwellian viscoelastic behavior. The
theory elucidates the most essential features of rheological behavior of polysaccharide associating systems (with A = adamantyl
moiety, C = β-cyclodextrin, B = either chitosan or hyaluronan) including similar behavior of G
′ and G
″ in a wide frequency range, strong temperature dependence of the characteristic frequency ω
x
, and an extremely strong effect of added free stickers (fC) on the dynamics.
This paper was presented at Annual European Rheology Conference (AERC) held in Hersonisos, Crete, Greece, April 27–29, 2006. 相似文献
3.
Summary The concept of a diffusion-averaged molecular weight, Md is presented, and Md is defined for polydisperse samples. It is shown via oligostyrene mixtures that Md can be determined in 20 minutes with common chromatographic equipment. If Md is measured and Mn or Mw is known, the polydispersity can be obtained. 相似文献
4.
Summary The successful application of the formerly presented concept of diffusion-averaged molecular weight, Md, to vacuum residues of crude oils, or their fractions, is described. The samples for establishing the calibration curve, logDvs. logM, were crude oil fractions with polydispersities smaller than 1.1. In a surprisingly good approximation the calibration curve is independent of the origin of these fractions if 500<M<10000. The validity of our calibration curve was demonstrated with more than 10 crude oil residues and with some of their hydrogenation residues [2]. 相似文献
5.
Olaf Evers Erich Hdicke Gregor Ley 《Colloids and surfaces. A, Physicochemical and engineering aspects》1994,90(2-3):135-147
The self-consistent mean field model of Scheutjens and Fleer is used to model spherical aggregates of homopolymers and monomer—polymer particles in solution. For homopolymer aggregates we found that the chain ends are preferentially located at the exterior side of the polymer/solvent interface. The distribution of the end segments may be an important parameter in latex film formation. For monomer—polymer particles a “core-shell” structure is found with an extended core containing a monomer—polymer mixture and a thin shell a few nanometres thick strongly enriched with monomer. The monomer-enriched shell seems to function as a solvating envelope for the dangling chain ends. These results are compared with other simulations based on a single chain in a spherical-cavity model. 相似文献
6.
V. Peikov I. Petkanchin S. P. Stoylov 《Journal of Dispersion Science and Technology》2013,34(4):499-512
Electric light scattering method is used for revealing the presence of aggregates in very diluted aqueous α-FeOOH suspensions. Three theoretical models are used for the geometrical form of aggregates. The comparison between the electro-optical results -theoretical and experimental - shows that even in the most diluted suspensions exist aggregates with irregular form. Using the comparison between electron microscopy and electro-optical results the geometric shape of the aggregates is determined. 相似文献
7.
Network polymers in a rubber or a gel often contain non-uniform chain lengths. By means of dynamic Monte Carlo simulations of polymer mixtures with various compositions of two chain lengths, we investigated how the factor of polydispersity influences their strain-induced crystal nucleation. Under a high temperature and a high strain rate, the stretching of both polymers revealed that crystal nucleation is mainly accelerated by the presence of short-chain polymers; nevertheless, both polymers join together in the nucleation process. Further analysis proved that crystal nucleation is initiated from those highly stretched short segments, which are rich on the short-chain polymers. 相似文献
8.
The self-consistent field theory has been employed to numerically study the response of bi-disperse flexible polyelectrolyte (PE) brushes grafted on an electrode to electric fields generated by opposite surface charges on the PE-grafted electrode and a second parallel electrode. The numerical study reveals that, under a positive external electric field, the shorter and negatively charged PE chains are more responsive than the longer PE chains in terms of the relative changes in their respective brush heights. Whereas under a negative external electric field, the opposite was observed. The total electric force on the grafted PE chains was calculated and it was found that, under a positive external electric field, the magnitude of the total electric force acting on one shorter PE chain is larger than that on one longer PE chain, or vice versa. The underlying mechanism was unraveled through analyzing the total electric field across the two oppositely charged electrodes. 相似文献
9.
10.
Florian J. Stadler Christian Piel Joachim Kaschta Sascha Rulhoff Walter Kaminsky Helmut Münstedt 《Rheologica Acta》2006,45(5):755-764
Linear high-density polyethylenes with molar masses M
w between 240 and 1,000,000 g/mol, obtained by metallocene catalysts, were characterized in shear using oscillatory and creep tests. The polydispersities of the molar mass distributions (MMDs) lay between 1 and 16. The resulting zero shear-rate viscosities η0 covered a range from 2.5×10−3 to around 108 Pas. Above a critical molar mass of M
c≈2,900 g/mol, the experimental results can be described by the relation η0 ∼ M
w3.6, independently of the MMD. The oscillatory data were fitted with a Carreau–Yasuda equation. The resulting parameters were correlated to molecular structure. The parameter a, being a quantity for the width of the transition between the Newtonian and the non-Newtonian regime, showed a dependence on the molar mass M
w but not on M
w/M
n. The parameter λ of the Carreau-Yasuda equation was found to be the reciprocal crossover frequency for all samples with a log-Gaussian MMD. λ depends on the molar mass M
w and also on M
w/M
n.
相似文献
Helmut MünstedtEmail: Phone: +49-9131-8527604Fax: +49-9131-8528321 |