Local structure theory: Calculation on hexagonal arrays,and interaction of rule and lattice

Local structure theory calculations⁷ are applied to the study of cellular automata on the two-dimensional hexagonal lattice. A particular hexagonal lattice rule denoted (3422) is considered in detail. This rule has many features in common with Conway'sLife. The local structure theory captures many of the statistical properties of this rule; this supports hypotheses raised by a study ofLife itself⁽⁶⁾. As inLife, the state of a cell under (3422) depends only on the state of the cell itself and the sum of states in its neighborhood at the previous time step. This property implies that evolution rules which operate in the same way can be studied on different lattices. The differences between the behavior of these rules on different lattices are dramatic. The mean field theory cannot reflect these differences. However, a generalization of the mean field theory, the local structure theory, does account for the rule-lattice interaction.     

Duality in algebra and topology

We apply ideas from commutative algebra, and Morita theory to algebraic topology using ring spectra. This allows us to prove new duality results in algebra and topology, and to view (1) Poincaré duality for manifolds, (2) Gorenstein duality for commutative rings, (3) Benson–Carlson duality for cohomology rings of finite groups, (4) Poincaré duality for groups and (5) Gross–Hopkins duality in chromatic stable homotopy theory as examples of a single phenomenon.     

The Domany-Kinzel cellular automaton phase diagram

The boundaries between the three phases of the Domany-Kinzel probabilistic cellular automaton are determined with high accuracy via the gradient method. The difficulties the extrapolation to the thermodynamic limit are circumvented and the critical exponents are also presented.     

Fractal aggregates induced by liposome-liposome interaction in the presence of Ca2+

We present a study of the fractal dimension of clusters of large unilamellar vesicles (LUVs) formed by egg yolk phosphatidylcholine (EYPC), dimyristoylphosphocholine (DMPC) and dipalmitoylphosphocholine (DPPC) induced by Ca²⁺ . Fractal dimensions were calculated by application of two methods, measuring the angular dependency of the light scattered by the clusters and following the evolution of the cluster size. In all cases, the fractal dimensions fell in the range from 2.1 to 1.8, corresponding to two regimes: diffusion-limited cluster aggregation (DLCA) and reaction-limited cluster aggregation (RLCA). Whereas DMPC clusters showed a typical transition from the RLCA to the DLCA aggregation, EYPC exhibited an unusual behaviour, since the aggregation was limited for a higher concentration than the critical aggregation concentration. The behaviour of DPPC was intermediate, with a transition from the RLCA to the DLCA regimes with cluster sizes depending on Ca²⁺ concentration. Studies on the reversibility of the aggregates show that EYPC and DPPC clusters can be re-dispersed by dilution with water. DMPC does not present reversibility. Reversibility is evidence of the existence of secondary minima in the DLVO potential between two liposomes. To predict these secondary minima, a correction of the DLVO model was necessary taking into account a repulsive force of hydration.     

Decoupling and recoupling of detonation waves associated with sudden expansion

Detonation propagation behavior associated with sudden expansions has been investigated both experimentally and numerically. Different mechanisms, from sustained propagation to detonation failure and reinitiation including shock and flame front decoupling and recoupling have been observed with the schlieren technique. The shock-induced flame propagation has been modeled with two-step chemistry and structured two-dimensional CFD on arbitrary geometries. The results of the numerical simulations show good correspondence to the variety of phenomena observed in experiments. Thus the numerical simulation can be used to study detonation propagation in complex geometries. It provides a tool for the design of safety devices and aids experimental investigations. Received 4 August 1995 / Accepted 25 April 1996     

Bi-functional optimization of actively cooled, pressurized hollow sandwich cylinders with prismatic cores

All metallic, hollow sandwich cylinders having ultralight two-dimensional (2D) prismatic cores are optimally designed for maximum thermo-mechanical performance at minimum mass. The heated cylinder is subjected to uniform internal pressure and actively cooled by forced air convection. The use of two different core topologies is exploited: square- and triangular-celled cores. The minimum mass design model is so defined that three failure modes are prevented: facesheet yielding, core member yielding, and core member buckling. The intersection-of-asymptotes method, in conjunction with the fin analogy model, is employed to build the optimization model for maximum heat transfer rate. A non-dimensional parameter is introduced to couple the two objectives—structural and thermal—in a single cost function. It is found that the geometry corresponding to maximum heat transfer rate is not unique, and square-celled core sandwich cylinders outperform those having triangular cells. The eight-layered sandwich cylinders with square cells have the best overall performance in comparison with other core topologies. Whilst a sandwich cylinder with shorter length is preferred for enhanced thermo-mechanical performance, the influence of the outer radius of the cylinder is rather weak.     

H_2—O_2爆轰时Ar浓度对产生胞格结构的影响

作者在方形爆轰管中进行了H_2—O_2—Ar系统的实验研究。在由Ar稀释的H_2—O_2混合物的爆轰实验中得到了规则的胞格结构图案。也得到了胞格形成的临界曲线,并与爆炸极限曲线进行了对照,两者的趋势是一致的。另外,测量了从点火处到胞格形成处之间的距离及胞格区的长度。最后分析了氩Ar浓度对H_2—O_2爆轰的抑制作用。     

Aqueous Self‐Assembly of Purely Hydrophilic Block Copolymers into Giant Vesicles

Self‐assembly of macromolecules is fundamental to life itself, and historically, these systems have been primitively mimicked by the development of amphiphilic systems, driven by the hydrophobic effect. Herein, we demonstrate that self‐assembly of purely hydrophilic systems can be readily achieved with similar ease and success. We have synthesized double hydrophilic block copolymers from polysaccharides and poly(ethylene oxide) or poly(sarcosine) to yield high molar mass diblock copolymers through oxime chemistry. These hydrophilic materials can easily assemble into nanosized (<500 nm) and microsized (>5 μm) polymeric vesicles depending on concentration and diblock composition. Because of the solely hydrophilic nature of these materials, we expect them to be extraordinarily water permeable systems that would be well suited for use as cellular mimics.     

Self‐Assembly and Disassembly of Vesicles as Controlled by Anion–π Interactions

Anion–π interactions have been widely studied as new noncovalent driving forces in supramolecular chemistry. However, self‐assembly induced by anion–π interactions is still largely unexplored. Herein we report the formation of supramolecular amphiphiles through anion–π interactions, and the subsequent formation of self‐assembled vesicles in water. With the π receptor 1 as the host and anionic amphiphiles, such as sodium dodecylsulfate (SDS), sodium laurate (SLA), and sodium methyl dodecylphosphonate (SDP), as guests, the sequential formation of host–guest supramolecular amphiphiles and self‐assembled vesicles was demonstrated by SEM, TEM, DLS, and XRD techniques. The intrinsic anion–π interactions between 1 and the anionic amphiphiles were confirmed by crystal diffraction, HRMS analysis, and DFT calculations. Furthermore, the controlled disassembly of the vesicles was promoted by competing anions, such as NO₃^?, Cl^?, and Br^?, or by changing the pH value of the medium.