Neighborhood unions and the cycle cover number of a graph

For several years, the study of neighborhood unions of graphs has given rise to important structural consequences of graphs. In particular, neighborhood conditions that give rise to hamiltonian cycles have been considered in depth. In this paper we generalize these approaches to give a bound on the smallest number of cycles in G containing all the vertices of G. We show that if for all x, y ? V(G), |N(x) ∩ N(y)| ≧ 2n/5 + 1, then V(G) is coverable by at most two cycles. Several related results and extensions to t cycles are also given.     

The influence of hard‐segments on two‐phase structure and shape memory properties of PCL‐based segmented polyurethanes

Poly(ε‐caprolactone)‐based segmented polyurethanes (PCLUs) were prepared from poly(ε‐caprolactone) diol, diisocyanates (DI), and 1,4‐butanediol. The DIs used were 4,4′‐diphenylmethane diisocyanate (MDI), 2,4‐toluenediisocyanate (TDI), isophorone diisocyanate (IPDI), and hexamethylene diisocyanate (HDI). Differential scanning calorimetry, small‐angle X‐ray scattering, and dynamic mechanical analysis were employed to characterize the two‐phase structures of all PCLUs. It was found that HDI‐ and MDI‐based PCLUs had higher degree of microphase separation than did IPDI‐ and TDI‐based PCLUs, which was primarily due to the crystallization of HDI‐ and MDI‐based hard‐segments. As a result, the HDI‐based PCLU exhibited the highest recovery force up to 6 MPa and slowest stress relaxation with increasing temperature. Besides, it was found that the partial damage in hard‐segment domains during the sample deformation was responsible for the incomplete shape‐recovery of PCLUs after the first deformation, but the damage did not develop during the subsequent deformation. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 557–570, 2007     

Photoinitiated cationic polymerization of cycloaliphatic epoxide with siloxane or alkoxysilane functionalized polyol coatings

Polyols were reacted with tetraethyl orthosilicate (TEOS) or 3-isocyanatopropyltriethoxysilane (IPTES) to form siloxane functionalized polyols. The UV-reactivity of these siloxane functionalized polyols were investigated using real-time FT-IR spectroscopy. The reactivity of TEOS modified polyols was dependent on the relative humidity. However, for the IPTES functionalized polyols the effect of relative humidity was dependent on the degree of IPTES functionalization. When the polyols were only partially functionalized with IPTES, the effect of relative humidity was minimal. However, when polyols were fully functionalized with IPTES, the curing was dependent on relative humidity. The siloxane functionalized polyols were formulated with a cycloaliphatic epoxide and cationic photoinitiator. The photo-induced curing kinetics of these cycloaliphatic epoxide/siloxane functionalized polyol coatings were also investigated. Unlike the TEOS functionalized polyols, the addition of IPTES functionalized polyols into the formulation inhibited the curing speed. This inhibition was attributed to the basicity nitrogen of the urethane linkage. The effect of relative humidity on the UV-curing reaction of cycloaliphatic epoxide coatings was lowered by the incorporation of the TEOS functionalized polyols.     

Flow-injection spectrophotometric determination of sulfadiazine and sulfamethoxazole in pharmaceuticals and urine.

A rapid and sensitive flow-injection spectrophotometric method is proposed for the determination of sulfadiazine and sulfamethoxazole. This method is based on the diazotization of sulfonamide with sodium nitrite, and a coupling reaction of the diazo-compound with alpha-naphthylamine. The optimum experimental conditions are obtained by using the controlled and weighted centroid simplex method. The linear ranges for the determination of sulfadiazine and sulfamethoxazole are 0.2-20 microg ml(-1) and 0.1-20 microg ml(-1), and their detection limits are 0.06 microg ml(-1) and 0.05 microg ml(-1), respectively, and the sampling frequency is 130 samples per hour. The method has been used to determine sulfadiazine and sulfamethoxazole in pharmaceuticals and urine without separation. The results are in agreement with those obtained by a high-performance liquid chromatograph technique at the 95% confidence level.     

An algorithm for three-way data analysis that alternatively minimizes coupled vector (COV) resolution error and PARAFAC error.

A novel algorithm, alternatively minimizing coupled vector (COV) resolution error and PARAFAC error algorithm, is proposed in this paper. This algorithm can overcome the problem of slow convergence and is insensitive to the estimation of component number, such problems are unavoidable while using the traditional parallel factors analysis (PARAFAC) algorithm. In other words, this algorithm is capable of improving the computing speed and providing accurate resolutions provided that the number of factors used in the computation is no less than that of the actual underlying ones. The characteristic performances were demonstrated with a novel fluorescence data array.     

ANTI FUZZY VECTOR SPACES（Ⅱ）

ＡＮＴＩＦＵＺＺＹＶＥＣＴＯＲＳＰＡＣＥＳ（Ⅱ）ＣｈｅｎＹｏｎｇｎｉａｎ（ＤｅｐａｒｔｍｅｎｔｏｆＭａｔｈｅｍａｔｉｃｓ，ＸｉｎｊｉａｎｇＮｏｒｍａｌＵｎｉｖｅｒｓｉｔｙ，８３００５４，Ｘｉｎｊｉａｎｇ，Ｐ．Ｒ．Ｃｈｉｎａ）ＡＮＴＩＦＵＺＺＹＶＥＣＴ...     

Synthesis and transition temperatures of liquid crystals incorporating a 1,4-tetrafluorophenylene unit

Two homologous series of mesogenic materials which incorporate a 1,4-tetrafluorophenylene moiety and a terminal cyano- or nitro-substituent have been synthesized by using palladiumcatalysed coupling procedures. The compounds exhibit nematic and/or smectic A phases.     

Continuous preparation of decorated nano zinc oxide organic sols with intense luminescence

A sort of decorated nano ZnO organic sols have been successively prepared by pulsed laser ablation at the interface of ZnO target and a flowing liquid containing polymers. It is found that the decorated nano ZnO ethanol sols, the decorated nano ZnO-PS (polystyrene) cyclohexane sols and the decorated nano ZnO-PMMA (polymethyl methacrylate) ethyl butyrate sols all have strong fluorescence emission at 329 nm and 411 nm, 308 nm and 317 nm, and at 330 nm and 400 nm, respectively. The results show the decorating for nano ZnO will intensely affect their luminescence, and the wavelength and intensity of luminescence can be adjusted or controlled by the different decoration.     

Synthesis of grafted poly(p‐phenyleneethynylene) with energy donor–acceptor architecture via atom transfer radical polymerization: Towards nonaggregating and hole‐facilitating light‐emitting material

In this contribution, we demonstrate a new effective methodology for constructing highly efficient and durable poly(p‐phenyleneethynylene) (PPE) containing emissive material with nonaggregating and hole‐facilitating properties through the introduction of hole‐transporting blocks into the PPE system as the grafting coils as well as building the energy donor–acceptor architecture between the grafting coils and the PPE backbone. Poly(2‐(carbazol‐9‐yl)ethyl methacrylate) (PCzEMA), herein, is chosen as the hole‐transporting blocks, and incorporated into the PPE system as the grafting coils via atom transfer radical polymerization. The chemical structure of the resultant copolymer, PPE‐g‐PCzEMA, was characterized by NMR and gel permeation chromatography, showing that the desirable copolymer was obtained with the narrow polydispersity. The increased thermal stability of PPE‐g‐PCzEMA was confirmed by thermogravimetric analysis and differential scanning calorimetry along with its macroinitiator. The optoelectronic properties of this copolymer were studied in detail by ultraviolet‐visible absorption, photoluminescence emission and excitation spectra, and cyclic voltammogram (CV). The results indicate that PPE‐g‐PCzEMA exhibits the solid‐state luminescent property dominated by individual lumophores, and also the energy transfer process from the PCzEMA blocks to the PPE backbone with a relatively higher energy transfer efficiency in the solid‐state compared to that of the solution state. Additionally, the hole‐injection property is greatly facilitated due to the presence of PCzEMA, as confirmed by CV profiles. All these data indicate that PPE‐g‐PCzEMA is a good candidate for use in optoelectronic devices. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3776–3787, 2007