AP/HTPB复合推进剂用纳米Co粉的制备

以CoCl_2·H_2O和水合联氨(N_2H_4·H_2O)为主要原料,采用化学还原法制备了纳米Co粉.在不同工艺条件下制备了树枝状纳米Co粉和球形纳米Co粉,用TEM和XRD对产物进行了表征,同时用DTA测试了加入球形纳米Co粉后AP的热分解性能.结果表明,反应介质的黏度和分散剂性质对纳米Co粉粒度及形貌影响较大,在最佳工艺条件下制备了颗粒尺寸均匀、粒度为50~60 nm的球形纳米Co粉;球形纳米Co粉能使AP热分解反应的高温分解峰温度显著下降;添加质量分数2%的球形纳米Co粉,复合推进剂的燃速明显提高,压力指数大幅降低.     

酯对钼系Ziegler-Natta催化剂引发丁二烯聚合的影响

以MoCl_4(Mo)为主催化剂,甲苯氧基二异丁基铝(Al)为助催化剂,在加氢汽油溶剂中,研究了8种酯对丁二烯(Bd)聚合的影响。结果表明,凡是能够溶解在酯中的Mo与Al所组成的二元催化体系,大多能很好地引发Bd聚合,并有较高的催化活性。酯的主要作用是增加Mo在加氢汽油中的溶解性,对聚合物的分子量影响不大,对微观结构几乎无影响。     

再生丁基橡胶与非极性不饱和橡胶共混物的性能研究

对再生丁基橡胶(RIIR)与非极性不饱和橡胶共混物的性能进行了研究。结果表明,RIIR易以填料的形式加入到非极性不饱和橡胶中使用,当RIIR以填料的形式加入到NR、BR及SBR中时,不仅使它们的耐热氧老化性及耐屈挠龟裂性得到明显改善,而且使NR及BR的撕裂强度及扯断伸长率提高;RIIR作为生胶与BR及NR共混,可改善BR的耐热氧老化性,提高NR的撕裂强度;SBR与RIIR共混,均使拉伸强度及撕裂强度降低;非极性不饱和二烯类橡胶与RIIR共混后,均使耐磨性降低。     

丁羟包覆层的黏超弹本构模型

为了准确地描述丁羟（HTPB）包覆层在有限变形下的拉伸力学特性,研究了HTPB包覆层的黏超弹本构模型。分别构建了含率相关函数的本构模型和并联式本构模型,前者由超弹模型与率相关项相乘得到,后者由超弹模型与含损伤因子的黏弹模型并联而成。进行了HTPB包覆层的单步松弛、多步松弛和不同速率的单轴拉伸试验,并将试验数据用于拟合模型参数。结果表明,HTPB包覆层对应变率极其敏感,且具有很大的延伸率,表现出明显的黏超弹特性;两种模型均能很好地预测HTPB包覆层较大形变范围内的拉伸力学性能,其中含率相关函数的模型的描述更加准确,其研究具有重要的军事意义。     

Dynamic-mechanical properties of polybutadiene rubbers

The dynamic properties of high-cis (98%) and cis-trans (42% cis) polybutadienes, crosslinked with 0.1 to 1.0% of crosslinking agent, have been studied using a torsion pendulum method over the temperature range ?170 to +20°C. For the high-cis rubber plots of damping factor (tan δ) against temperature showed the expected peak in the glass-transition region with an additional peak in the neighbourhood of 0°C attributable to crystallization. The cis-trans rubber showed two damping maxima in the transition region, separated by 30 to 40°C (depending on the degree of crosslinking), suggesting incipient phase separation of the component structures. The rebound resilience of the high-cis rubber at room temperature exceeded that of the cis-trans, reaching 92% at the highest crosslink density. Plots of resilience versus temperature for both rubbers showed a single minimum in the glass transition region.     

Linear viscoelastic properties of mixtures of 3- and 4-arm polybutadiene stars

The viscoelastic properties of a three-arm and a four-arm star polybutadiene with the same arm molecular weight (M_a) were studied. The zero-shear recoverable compliance (J⁰_e) and plateau modulus (G⁰_N) for these stars are the same. The zero-shear viscosity (η₀) of the three-arm star is 20% lower than that of the four-arm star. Mixtures of the stars had J⁰_e and G⁰_N unchanged. A $\text{50}\text{50}$ mixture of the three- and four-arm star was diluted with a low molecular weight linear polybutadiene. G⁰_N∝ø²; J⁰_e∝ø^?1 and M_e∝ø^?1, as expected for dilution with a θ-solvent.     

Differences in the molecular weight and the temperature dependences of self-diffusion and zero shear viscosity in linear polyethylene and hydrogenated polybutadiene

Within the context of a generalized coupling model we can support the hypothesis that, while the mode of relaxation for self diffusion (D) and shear flow (η) are the same, the entanglement interactions are different. We assume that there are two distinct coupling parameters n_D and n_η for self diffusion and shear flow respectively. The model predicts the molecular weight and temperature dependences to be scaled by the relevant coupling parameters as:

for melts with Arrhenius temperature dependences. We have found that n_n=0.43 and 0.42 for polyethylene (PE) and hydrogenated polybutadiene (HPB) which scale η as M^3.5 and M^3.4. Also the apparent flow activation energies $\text{E1}{}_{\mathrm{a}}$ of 6.35 kcal mole^?1 for PE and 7.2 kcal mol^?1 for HPB scale to primitive activation energies E_a of 3.6 and 4.2 kcal mole^?1 for PE and HPB respectively. On the other hand the M^?2 dependence of D results in n_D=1/3. Then the reported activation energies for self-diffusion in PE and HPB of 5.49 and 6.2 kcal mole^?1 scale to primitive activation energies of 3.7 and 4.1 kcal mole^?1, respectively.     

老化对丁羟推进剂燃速性能影响的试验研究

试验研究了贮存老化对HTPB复合固体推进剂燃速性能影响。分别采用自然老化和加速老化的试验方法,对HTPB推进剂在贮存过程中燃速的变化规律进行了对照分析。自然老化采用库房中贮存的方坯,加速老化采用热加速老化方法,燃速测定为水下声发射方法。试验结果表明,HTPB推进剂在贮存过程中燃速有随时间下降趋势,但变化不明显。自然老化与加速老化结论比较一致,具有可比性,这初步表明加速老化试验可以用于推算HTPB推进剂的燃速老化性能,所获得结论可以为固体火箭发动机进一步寿命评估作参考。分析了老化过程引起燃速性能变化的2种机理:化学老化引起的推进剂组分分解和物理老化引起的裂纹和空洞。前者使燃速产生减小的趋势,后者使燃速有增加的趋势,但总体而言,化学老化是主要的,老化的长期效应是燃速略有减小。     

火药用粘结剂研究进展过程分析

简要介绍已经实现批量生产和各国目前研究的几种代表性的粘结剂,通过分析比较其优缺点,提出了火药用粘结剂发展的趋势和研究中应注意的一些问题.