α-Methylstyrene/isobutene, α-methylstyrene/diisobutene, cyclopentadiene/isobutene, and cyclopentadiene/α-methylstyrene were copolymerized by cationic polymerization techniques. Several properties of the copolymers such as softening ranges and oxidation stability depend on their constitutional composition, and were controlled by variation of the conditions of their synthesis. 相似文献
Three different nitrocellulose (NC) samples produced from linters were investigated. DSC studies on the NC+sym-diethyldiphenylurea (C1) mixtures were carried out. The influence of storage time on their pore structures was examined using
thermoporometry. The results led to conclusion that large pores are multiples of small ones. The parameter n was used to characterize the number of C1 molecules equivalent to NC ring. Its value for short storage time was about 9 but
for longer time reached the value of 3. The influence of thermal history on the phase transition and porosity of the different
nitrocellulose samples was different. 相似文献
Solutions of Pyro grade nitrocellulose (NC) in dimethyl acetamide (DMA), containing between 42.5% and 60% NC (w/w), have been studied by differential scanning calorimetry and polarised light microscopy. The results showed that NC forms a lyotropic liquid crystal structure in DMA. A transition from the liquid crystal phase to an isotropic phase occurred over the temperature range 27 °C to 67 °C, and the enthalpy of transition increased with NC concentration. Rheological properties were determined using an extrusion rheometer with a slit die. The solutions were shown to have a yield stress for flow which increased with increasing NC concentration. The solutions were also found to be thixotropic. 相似文献
Complexes of nitrocellulose (NC – low and high nitrogen content) with copper oxide (CuO) have been synthesized and studied
for morphological behaviour on heating from room temperature to 500°C with the help of hot stage microscopy (HSM).
During decomposition, NC:CuO complexes show contraction of fibrous boundaries followed by mass movement of matrix, with the
evolution of brown yellow colour gas at higher temperatures as compared to NC alone.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
Summary: Dynamic mechanical analysis is combined with mass spectrometry to study nitrocellulose under oscillating strain. At a constant temperature (150–160 °C) and frequency (400–600 Hz) nitrocellulose fractures demonstrating a modulus drop and release of products with m/z: 30 and 44. At linear heating (2 °C · min−1) and a frequency of 10–50 Hz similar products are released in two steps, the second of which demonstrates a modulus drop and a temperature increase indicating ignition.
Data for an isothermal dynamic mechanical analysis–mass spectrometry experiment performed at 160 °C. 相似文献
A unique approach of developing a bar code version of lateral-flow enzymatic-based assay for the semi-quantification of hydrogen peroxide is described. The proposed assay system is mainly composed of a goat anti-mouse IgG-horseradish peroxidase conjugate (Gt anti-M IgG-HRP)-coated nitrocellulose (NC) membrane and a peroxidase substrate pad. Unlike the bar code immunochromatographic assay which depends on the stepwise capture of analyte, the principle of enzyme-based bar code lateral-flow assay is based on the different reaction time on successive lines due to the delay in 3,3′,5,5′-tetramethylbenzidine (TMB) release. Hydrogen peroxide (H2O2) acts as a limiting factor which controls the rate of the enzymatic conversion of TMB to blue color complex. The system expresses the concentration of H2O2 in micromole range as three distinct ladder bars in 9 min therefore without the need of any reading device. The major advantages of this assay are its easily readable result, and also its simplicity and low-cost in production offers a cheaper alternative for testing those expensive biosensors might not be available to the third world countries. By incorporating with H2O2-generating oxidoreductases, the assay can be further extended to detect a variety of analytes with clinical and environmental importance. Glucose was chosen to be the model analyte where the proposed system gave signal response at between 5 μM and 100 μM. 相似文献