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51.
N-(1,3-Thiazol-5(4H)-ylidene)amines via 1,3-Dipolar Cycloaddition of Azides and 1,3-Thiazol-5(4H)-thiones Organic azides 5 and 4,4-dimethyl-2-phenyl-1,3-thiazol-5(4H)-thione ( 2 ) in toluene at 90° react to give the corresponding N-(1,3-thiazol-5(4H)-ylidene)amines (= 1,3-thiazol-5(4H)-imines) 6 in good yield (Table). A reaction mechanism for the formation of these scarcely investigated thiazole derivatives is formulated in Scheme 3: 1,3-Dipolar azide cycloaddition onto the C?S group of 2 leads to the 1:1 adduct C . Successive elimination of N2 and S yields 6 , probably via an intermediate thiaziridine E . 相似文献
52.
Hakan Kaygusuz F. Bedia Erim Önder Pekcan Gülşen Akın Evingür 《Journal of fluorescence》2014,24(1):161-167
In this study, spherical alginate beads containing pyranine (P y ) as a fluorescence probe were prepared by ionotropic gelation of a sodium alginate solution. The steady state fluorescence technique was used to study pyranine release from the alginate beads crosslinked with calcium, barium and aluminum ions, respectively. The slow release of P y was observed with the time drive mode of the spectrophotometer at 512 nm. Fluorescence emission intensity (I p ) from P y was monitored during the release process, and the encapsulation efficiency (EE) of pyranine from the alginate beads was calculated. The Fickian Diffusion model was used to measure the release coefficients, D sl . It was seen that the slow release coefficients of pyranine from the alginate beads crosslinked with Ca2+, Ba2+, and Al3+ ions increased in the following order: D sl (Al3+)> D sl (Ca2+)> D sl (Ba2+). In contrast, the initial amount of pyranine and EE into the beads showed the reverse behavior. 相似文献
53.
A photo-differential scanning calorimetric (Photo-DSC) technique was used to study the photoinitiated radical polymerization of a 75% epoxy diacrylate (EA) and 25% tripropyleneglycoldiacrylate (TPGDA) mixture with 2-mercaptothioxanthone (TX-SH) as photoinitiator by using different light intensities. Photopolymerization reactions were carried out under identical conditions of temperature and initiator concentration. It was observed that all conversion curves during gelation at various UV light intensities present good sigmoidal behavior as predicted by the percolation model. Observations around the critical time, called the glass transition point (tg), taken for polymerization to reach the maximum rate (Rp max) show that the gel fraction exponents β obeyed the universal percolation picture. On the other hand, Rp max, t g, and final conversion values were found to be dependent on the UV light intensity. 相似文献
54.
The Susceptible-Infected-Recovered (SIR) and Susceptible-Exposed-Infected-Recovered (SEIR) models describe the spread of epidemics in a society. In the typical case, the ratio of the susceptible individuals fall from a value S 0 close to 1 to a final value Sf , while the ratio of recovered individuals rise from 0 to Rf?=?1???Sf . The sharp passage from the level zero to the level Rf allows also the modeling of phase transitions by the number of “recovered” individuals R(t) of the SIR or SEIR model. In this article, we model the sol–gel transition for polyacrylamide–sodium alginate (SA) composite with different concentrations of SA as SIR and SEIR dynamical systems by solving the corresponding differential equations numerically and we show that the phase transitions of “classical” and “percolation” types are represented, respectively, by the SEIR and SIR models. 相似文献
55.
Effects of multiwall carbon nanotube (MWCNT) addition on the electrical conductivities, optical transparencies and fluorescence emissions of poly(vinyl acetate-co-butyl acrylate) (P(VAc-co-BuA))/MWCNT composite films were studied. Optical transmission, fluorescence emission and two point probe resistivity techniques were used to determine the variations of the optical, fluorescence and electrical properties of the composites, respectively. Transmitted photon intensity (I tr), fluorescence emission intensity (I fl) and surface resistivity (ρ s) of the composite films were monitored as a function of MWCNT mass fraction (M) at room temperature. All these measured quantities of the composites were decreased by increasing the content of MWCNT in the composite. The conductivity and the optical results were attributed to the classical and site percolation theories, respectively. The fluorescence results, however, possessed both the site and classical percolation theories at low and high MWCNT content regions, respectively. 相似文献
56.
Effects of graphene nanoplatelet (GNP) addition on the electrical conductivity and optical absorbance of poly(methyl methacrylate)/graphene nanoplatelet (PMMA/GNP) composite films were studied. Optical absorbance and two point probe resistivity techniques were used to determine the variations of the optical and electrical properties of the composites, respectively. Absorbance intensity, A, and surface resistivity, Rs, of the composite films were monitored as a function of GNP mass fraction (M) at room temperature. Absorbance intensity values of the composites were increased and surface resistivity values were decreased by increasing the content of GNP in the composite. Electrical and optical percolation thresholds of composite films were determined as Mσ = 27.5 wt.% and Mop = 26.6 wt.%, respectively. The conductivity and the optical results were attributed to the classical and site percolation theories, respectively. Optical (βop) and electrical (βσ) critical exponents were calculated as 0.40 and 1.71, respectively. 相似文献
57.
Latex films have been prepared by annealing pyrene (Py)-labeled poly(methyl methacrylate)-polyisobutylene particles at the glass transition temperature (100 degrees C). These films were then irradiated by gamma rays from (60)Co in a gamma cell at room temperature at various dose rates (rad/h). Before dissolution the films were annealed at 200 degrees C for a 30 min time interval to complete the film formation process. Steady-state fluorescence techniques were used to monitor the dissolution of irradiated latex films. Dissolution of films in a chloroform-heptane (80%-20%) mixture was monitored in real time by the Py fluorescence intensity change. Relaxation constants, k(0), and dissolution coefficients, D(d), of polymer chains were measured. Two different regimes of D(d) values were observed during dissolution, which are related to two different molecular weight distributions caused by scission and branching of polymer chains when they were irradiated and annealed. Copyright 2001 Academic Press. 相似文献
58.
Two novel colorimetric receptors, S1 and S2, linked to one or two nitrophenylurea groups were synthesized in good yields, characterized and their chromogenic properties investigated towards various anions (F?, Cl?, Br?, I?, NO3?, AcO?, ClO4?, HSO4?, and H2PO4?) by UV–vis and 1H NMR techniques. The receptors, effectively and selectively, recognized and distinguished the biologically important F? from other anions such as Cl?, Br?, I? etc. in CH3CN. This selectivity could be easily observed by the naked eye, indicating that receptors S1 and S2 are potential colorimetric sensors for fluoride ion. 相似文献
59.
This work reports the encapsulation of latex particles in Al2O3-polystyrene (PS) composite films. These films were prepared from PS particles in Al2O3 dispersion at room temperature in various latex contents. Composite films were annealed at elevated temperatures in 10 min time interval above the glass transition temperature (Tg) of polystyrene. Transmitted photon intensities, I(tr) were monitored after each annealing step. AFM micrographs were also used to observe the physical changes of the composite films during annealing. It was observed that latex particles are encapsulated above a critical Al2O3 content of 33 wt% which corresponds to the critical occupation probability of p(c) = 0.33 at which the film obey the site-percolation model with a critical exponent of 0.45. Below p(c), it was seen that complete latex film formation process took place, where transparency of the film was increased by annealing. 相似文献
60.
The manufacture of microencapsulated phase change materials suitable for the design of thermally enhanced fabrics 总被引:2,自引:0,他引:2
Thermal comfort of a fabric is one of the important tasks of the designers that require an engineering approach. In this study, we first aimed to establish a manufacturing technique based on in situ polymerization in order to accomplish the microencapsulation of phase change materials (PCMs) that can ultimately be used in different textile applications, i.e. incorporating such products into the multi-component non-conventional fabrics. This method is suitable for the laboratory-scale work as well as the industrial-scale one, considering some important issues like energy and time savings. Four types of polyurea-formaldehyde microcapsules containing different waxes and a control group of 100% shell material were produced and then examined by DSC, particle size and SEM analyses. Furthermore, we also focused on the contributions of microencapsulated PCMs to the thermal performances of fabrics of certain passive insulation characteristics for the given cold weather and physical activity conditions, based on the model developed for a multi-layer fabric system. 相似文献