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171.
In many-valued logic the decision of functional completeness is a basic and important problem, and the thorough solution to this problem depends on determining all maximal closed sets in the set of many-valued logic functions. It includes three famous problems, i.e., to determine all maximal closed sets in the set of the total, of the partial and of the unary many-valued logic functions, respectively. The first two problems have been completely solved ([1], [2], [8]), and the solution to the third problem boils down to determining all maximal subgroups in the k-degree symmetric group Sk, which is an open problem in the finite group theory. In this paper, all maximal closed sets in the set of unary p-valued logic functions are determined, where p is a prime. Mathematics Subject Classification: 03B50, 20B35. 相似文献
172.
Danch A. Lohner K. Ungerank M. Stelzer F. 《Journal of Thermal Analysis and Calorimetry》1998,54(1):161-170
Bis [(ω-(4′-cyanobiphenyl)-4-yl)oxy-n-alkyl]norborn-5-ene-2,3-dicarboxylate was polymerised via ring opening metathesis polymerisation
(ROMP). Two disubstituted polynorbornene derivatives both of cis configuration with different length of the side-chain were
studied. Differential scanning calorimetry (DSC) was used to study the effect of thermal history on the assignment of the
glass transition event associated with the biaxial orientation of a smectic phase. Glass transition temperatures, the change
of isobaric specific heats at Tg and the enthalpies of isotropisation were calculated. The DSC traces only show the classic step-wise change in Tg in some cases, giving the evidence that the amorphous domains are constrained and highly restricted in movement due to the
morphology developed as a result of the biaxial stretching. Based on the literature data of mono- and disubstituted polynorbornene
derivatives and our calorimetric experiments, the shape of Tg dependence on number of (CH2) units is interpreted. The origin of this shape is discussed.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
173.
174.
P. Guenoun M. Delsanti D. Gazeau J.W. Mays D.C. Cook M. Tirrell M. Tirrell L. Auvray 《The European Physical Journal B - Condensed Matter and Complex Systems》1998,1(1):77-86
Aqueous micellar solutions of ionic/neutral block copolymers have been studied by light scattering, small angle neutron scattering
and small angle X-ray scattering. We made use of a polymer comprised of a short hydrophobic block (polyethylene-propylene)
PEP and of a long polyelectrolytic block (polystyrene-sulfonate) PSSNa which has been shown previously to micellize in water.
The apparent polydispersity of these micelles is studied in detail, showing the existence of a few large aggregates coexisting
with the population of micelles. Solutions of micelles are found to order above some threshold in polymer concentration. The
order is liquid-like, as demonstrated by the evolution with concentration of the peak observed in the structure factor (), and the degree of order is found to be identical over a large range of concentrations (up to 20 wt%). Consistent values
of the aggregation number of the micelles are found by independent methods. The effect of salt addition on the order is found
to be weak.
Received: 19 June 1997 / Received in final form: 4 September 1997 / Accepted: 9 October 1997 相似文献
175.
176.
Adolfo M. Nemirovsky Maurício D. Coutinho-Filho 《Journal of statistical physics》1988,53(5-6):1139-1153
A field-theoretic representation is presented to count the number of configurations of a single self-avoiding walk on a hypercubic lattice ind dimensions with periodic boundary conditions. We evaluate the connectivity constant as a function of the fractionf of sites occupied by the polymer chain. The meanfield approximation is exact in the limit of infinite dimensions, and corrections to it in powers ofd
–1 can be systematically evaluated. The connectivity constant and the site entropy calculated throughout second order compare well with known results in two and three dimensions. We also find that the entropy per site develops a maximum atf1–(2d)–1. Ford=2 (d=3), this maximum occurs atf~0.80 (f~0.86) and its value is about 50% (30%) higher than the entropy per site of a Hamiltonian walk (f=1). 相似文献
177.
Using the ligand pyridazine-3,6-dicarboxylate (H2pzdc), a coordination polymer [Cd2(pzdc)2(H2O)4] was synthesized and characterized by elemental analysis, thermal analysis, IR and single-crystal X-ray diffraction. The complex crystallizes in the tetragonal system with space group I41/a. The crystallographic data are: a=1.470 6(4) nm, c=1.489 8(6) nm, V=3.222 0(19) nm3, Z=16, μ=2.725 mm-1, Dc=2.594 g·cm-3, R1=0.017 8, wR2=0.044 6. In the complex, the cadmium(Ⅱ) ions with the eight-coordinated dodecahedral geometry are linked by the pzdc ligands to generate one-dimensional chains, which are associated into the three-dimensional architecture via O-H…O hydrogen bonding. CCDC: 658853. 相似文献
178.
Hydrogel nanonetworks with functional core-shell structure 总被引:1,自引:0,他引:1
Nurettin Sahiner 《European Polymer Journal》2007,43(5):1709-1717
Nanohydrogel particles of poly(acrylonitrile-co-N-isopropylacrylamide (p(AN-c-NIPAM)) were synthesized using a microemulsion polymerization technique. Highly monodisperse nanohydrogel particles e.g. 50-150 nm, and various morphology such as core-shell and connected beads were obtained. It was shown that the shell thickness and the size of particles can be tuned by the monomer concentrations and their ratios as well as by the utilization of different crosslinkers. The hydrophobic core monomer, AN was converted to amidoxime groups to increase the hydrophilicity of the nanogels which provide more hydrophilic character and impart new functionality to the nanonetwork. Transmission electron microscopy (TEM), and dynamic light scattering (DLS) techniques were employed for the particle size characterizations. The amidoximation reaction was confirmed by FT-IR spectroscopy. 相似文献
179.
取向聚对苯二甲酸乙二酯纤维的非等温结晶动力学张志英,赵家森(天津纺织工学院材料科学系天津300160)关键词取向高聚物,聚对苯二甲酸乙二酯,非等温结晶,结晶动力学研究高聚物结晶动力学常用的等温方法有光透射法、密度法、显微镜法、X-射线衍射法、差示扫描... 相似文献
180.
The dynamic viscoelastic response of the two-phase polymer blend systems shows the characteristics of the thermorheologically complex materials. In this paper theoretical equations for describing the dynamic viscoelastic response of such polymer blend systems have been established by means of the mechanical modeling technique. The dynamic viscoelastic response of the blend systems at any blend composition can be predicted theoretically by using the equations established, provided that the dynamic viscoelastic response of the two pure components and the mechanical model parameters are known in advance. Thus, we provide an effective method for studying the dynamic mechanical properties and the molecular relaxation characteristics of the two-phase polymer blend systems. 相似文献