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1.
The montmorillonites (MMTs), layered, smectite-type silicates, were premodified by two different methods priorto the polymer melt intercalation. In one case MMTs were modified with cetyltrimethylammonium bromide (CTAB), andtermed as organomontmorillonites (OMMTs); in the other case MMTs were modified by nylon, and the products were calledmodified montmorillonites (MMMTs). The effects of CTAB and nylon on the MMTs were investigated by using TG andWAXD. The results show that interlayer spacings of CTAN and nylon modified MMTs are larger than that of sodium MMTs.Then, polyamide 66 (PA 66)/MMT nanocomposites were obtained through the method of melt intercalation of polymers. Thenanocomposites were characterized by WAXD, TEM and Molau experiments. The results indicate that the MMTs dispersehomogeneously in the PA 66 matrix. The mechanical properties of nanocomposites, such as tensile properties and flexuralproperties, were also measured and show a tendency to increase with increase of MMT content and reach the maximumvalues at 5phr MMT content. The heat distortion temperature (HDT) of the nanocomposites (7 phr) is about 32 K higher thanthat of pure PA 66.  相似文献   
2.
The thermal stability of heat-stabilised polyamide 66 in an oxidative environment is evaluated by DSC. The oxidative stability of the polyamide decreases as a result of repeated injection moulding. The results also indicate that the presence of glass fibres in the polyamide has a negative influence on the oxidative stability. Both isothermal and dynamic DSC measurements seem to be useful tools for assessing the stability of polyamides and there is a relationship between data determined using both procedures. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   
3.
尼龙66/蒙脱土复合材料结晶行为的研究   总被引:8,自引:0,他引:8  
在密炼机中采用熔融共混法制备蒙脱土重量分数为 2 5 %、4 5 %的尼龙 6 6 /蒙脱土复合材料 .通过DSC法对非等温结晶行为及在 2 2 8~ 2 4 0℃范围内的等温结晶行为进行研究 ,并与纯尼龙 6 6进行比较 .从其等温和非等温结晶行为的研究表明 ,蒙脱土起成核剂的作用 ,它的填入使尼龙 6 6结晶速率提高 ,但填料与基体间的相互作用使其链段运动困难 ,结晶活化能提高 ;在研究的填料含量变化范围内 ,结晶行为变化不大 ,并且找到该复合材料在 2 2 8~ 2 34℃范围结晶对温度的不敏感区 ;对非等温结晶过程分析 ,刘结平 莫志深方程是适用的 ,而Ozawa方程则是不适用的 .  相似文献   
4.
A novel microencapsulated red phosphorus (RP) was prepared through the molecular self-assembly of melamine cyanurate (MCA). Compared with the conventional encapsulated RP, MCA-encapsulated RP (MERP) shows simpler and more environment-friendly preparation process higher thermal stability and lower moisture absorption. With MERP filled in unreinforced polyamide 66 (PA66) and glass fiber (GF) reinforced PA66, flame retardant materials with satisfactory flame retardancy and mechanical performance can be obtained. The influence of the MCA/RP ratio on the flame retardancy as well as the condensed phase of MERP flame retardant PA66 was investigated to reveal the nitrogen-phosphorus (N-P) synergistic flame retarding effects between MCA and RP.  相似文献   
5.
TheW KP (N) algebra has been identified with the second Hamiltonian structure in theNth Hamiltonian pair of the KP hierarchy. In this Letter, by constructing the Miura map that decomposes the second Hamiltonian structure in theNth pair of the KP hierarchy, we show thatW KP (N) can also be decomposed toN independent copies ofW KP (1) algebras, therefore its free-field realization can be worked out by constructing free fields for each copy ofW KP (1) . In this way, the free fields may consist ofN + 2n number of bosons, among them, 2n are in pairs, wheren is an arbitrary integer between 1 andN. We also express the currents ofW KP (N) in terms of the currents ofNn copies of U(1) andn copies of SL(2,R) k algebras with levelk = 1. By reductions, we give similar results forW (N) andW 3 (2) algebra.  相似文献   
6.
The infinitely many symmetries with arbitrary functions of timet for the potential modified Kadomtsev-Petviashvilli equation are obtained by using a simple direct method. These symmetries constitute a generalization of the well-knownW algebra.  相似文献   
7.
A diffusion model of metal surface modification by plasma nitriding has been developed. This model takes into account the erosion effects at the plasma/solid interface occurring due to the ion bombardment of the surface. For constant sputtering rate, which is the usual situation during plasma nitriding, the growth of the sub-layers is well described by the analytical expressiong(t) =g 0,f –1 (t/t 0), whereg(t) is the sub-layer thickness at timet,g 0 andt 0 are parameters which depend on the treated material and plasma characteristics,f –1 is the inverse of the function — In(1 - x) + x), 0 x 1. Under negligible erosion effects, the expression forg(t) reduces to the parabolic law. The diffusion zone (substratum) growth does not follow the parabolic law as well. However, the deviation occurs after long plasma nitriding time. The model can be used for experimentally determining the effective diffusion coefficients and the erosion rate during plasma nitriding of metal surfaces.  相似文献   
8.
Radul has recently introduced a map from the Lie algebra of differential operators on the circle of W n . In this Letter, we extend this map to W KP (q) , a recently introduced one-parameter deformation of WKP - the second Hamiltonian structure of the KP hierarchy. We use this to give a short proof that W is the algebra of additional symmetries of the KP equation.  相似文献   
9.
In this paper, a new type of organophilic montmorillonites, co-treated by octadecylammonium and aminoundecanoic acid, were synthesized and applied to prepare nylon 66/montmorillonite nanocomposites via melt compounding in a twin extruder. WAXD and TEM characterization indicate that a disordered structure was derived and the montmorillonite platelets dispersed in nanoscale in the nylon 66 matrix. The nanocomposites with co-treated montmorillonite display comparatively higher strength and modulus compared to nylon 66 matrix.  相似文献   
10.
Ab initio SCF computations on the intrinsic preferences of the H+, CH 3 + and C2H 5 + cations towards the two principal sites of protonation or alkylation on cytosine, N3 or O2, show that this preference undergoes a continuous modification with the increase in size and complexity of the cation. N3 is the preferred site of fixation of H+, O2 the preferred site of C2H 5 + , while CH 3 + has no marked preference. The exchange repulsion term of the binding energy appears responsible for the preference of C2H 5 + for O2.This work was supported by the Ligue Francaise contre le Cancer and the National Foundation for Cancer Research (USA)  相似文献   
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