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1.
Controlling effective interactions and spatial dispersion of nanoparticles in multiblock copolymer melts 下载免费PDF全文
Debapriya Banerjee Kenneth S. Schweizer 《Journal of Polymer Science.Polymer Physics》2015,53(16):1098-1111
The microscopic Polymer Reference Interaction Site Model theory is employed to study, for the first time, the effective interactions, spatial organization, and miscibility of dilute spherical nanoparticles in non‐microphase separating, chemically heterogeneous, compositionally symmetric AB multiblock copolymer melts of varying monomer sequence or architecture. The dependence of nanoparticle wettability on copolymer sequence and chemistry results in interparticle potentials‐of‐mean force that are qualitatively different from homopolymers. An important prediction is the ability to improve nanoparticle dispersion via judicious choice of block length and monomer adsorption‐strengths which control both local surface segregation and chain connectivity induced packing constraints and frustration. The degree of dispersion also depends strongly on nanoparticle diameter relative to the block contour length. Small particles in copolymers with longer block lengths experience a more homopolymer‐like environment which renders them relatively insensitive to copolymer chemical heterogeneity and hinders dispersion. Larger particles (sufficiently larger than the monomer diameter) in copolymers of relatively short block lengths provide better dispersion than either a homopolymer or random copolymer. The theory also predicts a novel widening of the miscibility window for large particles upon increasing the overall molecular weight of copolymers composed of relatively long blocks. The influence of a positive chi‐parameter in the pure copolymer melt is briefly studied. Quantitative application to fullerenes in specific copolymers of experimental interest is performed, and miscibility predictions are made. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 1098–1111 相似文献
2.
The present report describes a method suitable for the indirect assay of hydroxyl radical (OH.), which is likely to be produced during reperfusion of ischemic myocardium. Isolated rat heart perfused by the Langendorff technique was subjected to 30 min of ischemia, followed by 30 min of reperfusion. Salicylic acid (2 mM) was added to the perfusion circuit to trap any OH. radical generated during the experiment. 2,5- and 2,3-dihydroxybenzoic acids (hydroxylated products of salicylic acid) were identified by authentic standards as well as by pure OH.-generating system using high-performance liquid chromatography with electrochemical detection. In addition to serving as a chemical trap for the detection of OH., salicylate attenuated myocardial reperfusion injury as evidenced by reduced formation of creatine kinase, decreased lipid peroxidation, and improved myocardial contractile functions during reperfusion. These results thus provide direct evidence for the presence of OH. in heart and link it to the myocardial reperfusion injury. 相似文献
3.
Natural rubber is reinforced with a novel type of grass fiber (Cyperus Tegetum Rox b). The effects of fiber loading of different mesh sizes on curing characteristics and mechanical properties of grass fiber filled natural rubber composite are studied. Since 400 mesh grass fiber loaded natural rubber composite shows superior mechanical properties, therefore the effect of silane coupling agent was studied for this particular composite. Here composites were prepared by using water leached grass fiber. Optimum cure time increases with the increase in fiber loading but the change in scorch time is less. The same trend of increase in optimum cure time is observed in the presence of Si69. But the value is higher compared to that of rubber composite without Si69. With increase in the fiber loading, modulus and hardness of the composite increases but tensile strength decreases. The mechanical properties of the composite, namely moduli at 200 and 300% elongation and hardness increase in the presence of Si69 but tensile strength is less compared to that of the composite without Si69. Elongation at break is not much affected due to the presence of Si69. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
4.
[reaction: see text] A facile and highly selective indium-mediated allylation of hydrazones utilizing BINOL ligands is described. Chiral (R)-3,3'-bistrifluoromethylBINOL afforded homoallylic amines in up to 97% ee with stoichiometric ligand. Employing only 10 mol % ligand afforded selectivity of up to 92% ee. 相似文献
5.
Subhasis Chakrabarti Ashim K. Maity T. N. Misra 《Journal of polymer science. Part A, Polymer chemistry》1992,30(8):1625-1631
Raman spectroscopy has been used to study solid-state photopolymerization reactions in dimethyl ester of α,α′-dicyano-p-phenylenediacrylic acid (p-CPAMe) and diethyl ester of p-phenylenediacrylic acid (p-PDAEt). The reactants and products were characterized by infrared and Raman spectroscopy. Excitation and emission spectra suggest that in p-CPAMe exciton–phonon coupling is strong, but in the other monomer it is very weak. Raman phonon spectroscopic study reveal that in both the samples the reaction mechanism is homogeneous in the initial stages. However, in the later stages the reaction becomes heterogeneous in p-PDAEt. In p-CPAMe the lattice becomes disordered with the progress of polymerization and finally becomes amorphous whereas in p-PDAEt the lattice remains highly ordered. © 1992 John Wiley & Sons, Inc. 相似文献
6.
2,8-Dimethyltricyclo[6.2.2.01,6]dodeca-2,5-diene-4,9-dione (
), 2,9-dimethyltricyclo [6.3.1.01,6]dodeca-2,5-diene-4,10-dione (
) and 2-methyltricyclo[6.3.1.01,6]dodeca-2,5-diene-4,10-dione (
) have been synthesised for entry into the ring systems of a few tetracyclic diterpenes. 相似文献
7.
Prasenjit Maity Susmit Basu Sumit Bhaduri Goutam Kumar Lahiri 《Journal of molecular catalysis. A, Chemical》2007,270(1-2):117-122
High nuclearity platinum carbonyl cluster anions (Chini's clusters) have been used as precursors to prepare a platinum nanocatalyst. The ionic polyelectrolyte poly(diallyldimethylammonium chloride) has been used as the support material for anchoring [Pt30(CO)60]2− via ion-pairing and subsequent stabilization of the nanoparticles. The polymer-supported material has been studied by spectroscopy (NIR, 13C NMR, and IR) and TEM before and after its use as a water soluble hydrogenation catalyst. The nanocatalyst is found to be effective for the chemoselective hydrogenation of olefinic, aldehydic and ketonic double bonds. For most of the substrates isolation of the product and reuse of the catalyst are extremely easy due to the automatic phase separation of the products from the catalyst. The spectral features of the fresh catalyst show retention of the carbonyl ligands and molecular identity of the parent cluster, but after use the carbonyl ligands appear to be lost. TEM of the supported material before and after use as a catalyst shows the presence of platinum nanoparticles with majority (≥70%) of the particles in the range of 2–6 nm. Smaller particles are dominant in the used catalyst and this observation is rationalized on the basis of the known reactivity of Chini's clusters with dihydrogen. 相似文献
8.
9.
Zinc ion (Zn2+) is an important and a most useful biological trace nutrient responsible for the activity of several enzymes. Zn2+ concentrations in the environment as well as in the human body increase beyond permissible limits as a consequence of its mining and widespread industrial applications. Such excess Zn2+ concentrations are toxic to humans and many aquatic organisms. The magnetic inertness and spin paired electronic configuration of Zn2+ makes it hard to detect by common analytical techniques. Therefore, fluorometric detection using chemosensor is the most effective tool for the environmental and biological detection of Zn2+. We have developed a novel pyridine-constrained bis(triazole-linked hydroxyquinoline) ligand as a reversible fluorescent chemosensor for Zn2+. The symmetrical ligand is highly selective for Zn2+ and fluoresces brightly upon complexation compared with other metal ions based on chelation-enhanced fluorescence mechanism. Interestingly, free ligand can be regenerated by treating the ligand–Zn2+ complex with aqueous ammonia. 相似文献
10.