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71.
油气运移的条件和油气运移的特征决定了油气藏的形成与分布。沾化凹陷南斜坡不整合面、断层以及各层系储集砂体的空间配置构成复杂的立体网络通道,决定了油气的运移,控制了油气分布。以断层为垂向运移通道的油气藏常在断层带附近多层叠置;以连通砂体为主要运移通道的油气藏常形成于距烃源层较近或相邻的层位;以不整合面作为运移通道往往可使油气长距离运移形成各种地层油气藏。沾化凹陷南斜坡的油气藏都是油气经过两种或多种输导层阶梯式运移而形成的。砂体、断层和不整合面组成的输导系统的末端和边缘是油气运移的重要指向区。 相似文献
72.
大规模定制为生产带来了变革和影响。针对新的生产方式的要求,根据推动大规模定制的过程方法和技术来分析他们对于质量控制产生的影响和要求,给出了大规模定制条件下的质量控制系统的建议,并给出了一个简要的系统模型。 相似文献
73.
A series of novel block polymers of polyurethane (PU) and chitosan have been prepared in two steps. The first step is the preparation of PU prepolymer, obtained from polytetramethylene oxide glycol (PTMO, Mn = 1000), isophrone diisocyanate (IPDI), and 2,2′-dimethylol propionic acid (DMPA), followed by ionizing PU prepolymer with triethylamine (TEA). The second step involves PU chain-extended by water-soluble chitosan of low molecular weight (Mn = 5000) by self-emulsion polymerization method. The sizes of the latex particles, morphology, and copolymer architecture have been characterized by dynamic light scattering (DLS), general tensile test, infrared spectroscopy (IR), surface contact angle measurement, and transmission electron microscopy (TEM). Furthermore, it shows that the addition of chitosan remarkably increases anticoagulative property of PU elastomers confirmed by the recalcification time. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
74.
Porous poly(vinyl alcohol) (PVA) membranes were prepared by a phase‐inversion method. The influence of chemical crosslinking and heat treatments on the swelling degree, resistance to compaction, mechanical strength, and morphology of porous PVA membranes was extensively studied. The crosslinking degree and crystallinity of the membranes, calculated from IR spectra, increased with the treatment time. The porosity, calculated on the basis of swelling experiments, showed a decreasing trend for heat‐treated membranes but remained almost at a constant value for crosslinked membranes. Such a change was further proved with scanning electron microscopy pictures. The behavior was explained by the rearrangement of PVA chains during the heat‐treatment process, which led to morphological changes in the membranes. The mechanical properties of the porous membranes in dry and wet states were measured, and a great difference was observed between crosslinked and heat‐treated membranes in the dry and wet states. The crosslinked membranes showed good mechanical properties in the dry state but became fragile in the wet state. On the contrary, the heat‐treated membranes were more flexible in the wet state than in the dry state. This change was explained by the turnaround of inner stress in the systems during the swelling process. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
75.
76.
本文全面分析了DH80—16型离心压缩机可倾轴瓦油封漏油的原因,并介绍了可倾轴瓦油封漏油问题的解决及具体实施方案。 相似文献
77.
78.
Wenying Wei Zhen Wang Yanhua Yin Jinyu Han Wen Xu 《Korean Journal of Chemical Engineering》2008,25(3):562-567
Composition Group Vector Space (CGVS) method for estimating melting and boiling point T
m
, T
b
of organic compound has been proposed, and the principle of this method has been elucidated. The models for estimating T
m
, T
b
have been established and the numerical values of relative parameters have been presented. The average percentage deviations
of T
m
, T
b
estimation are 7.53 and 1.58, respectively, which show that the present method demonstrates significant improvement in applicability
to predict the above properties, compared to conventional group methods. 相似文献
79.
Summary Well-defined water-soluble poly(styrenesulfonate)-b-poly(ethylene glycol)-b- poly(styrenesulfonate) (PSS-b-PEG-b-PSS) triblock
copolymers with narrow molecular weight distribution (1.29 < Mw/Mn < 1.36) were synthesized in aqueous solution at 70 oC via reversible addition-fragmentation chain transfer (RAFT) polymerization. The complex formed by the PSS-b-PEG-b-PSS triblock
copolymer coordinated with aluminum ion was investigated with turbidimetry, dynamic light scattering (DSL), zeta-potential,
and transmission electron microscopy (TEM). The aggregation formation was based on the neutralization of the SO3- groups in the PSS blocks with Al3+ ions. The appearance, size and stability of the PSS-b-PEG-b-PSS/Al3+ aggregates were controlled by varying the PSS block length and degree of neutralization (DN). At DN = 0.33, where the PSS-b-PEG-b-PSS
copolymer was completely neutralized with Al3+, the aggregate size increased with increasing PSS block length. The transition from the shrinking coil of small size to the
interchain aggregates of large size was found at DN of about 0.33. 相似文献
80.