研究固反应动力学和固过程的基终结聚乙烯 (HTPB) 推进剂
Zhiming Guo1,2, Yiliang Wang3, Michele Chiumsenti1
1Departament d'Enginyeria Civil i Ambiental (DECA), Universitat Politécnica de Catalunya (UPC), Jordi Girona 1, Barcelona, 08034, Spain.
Scientific reports
|July 1, 2025
概括
这项研究分析了基终结聚乙烯 (HTPB) 推进剂的固化. 较高的加热速度加快了固化,减少了加工时间,正如经过验证的模拟模型所证实的那样.
科学领域:
- 材料科学 材料科学 材料科学
- 化学工程是化学工程的重要组成部分.
- 航空航天工程 航空航天工程
背景情况:
- 基终结聚乙烯 (HTPB) 推进剂是关键的高性能固体推进剂.
- 它们的应用涵盖了航空航天和军事领域,需要优化性能和处理.
- 了解固化动力学对于推进剂的配方和制造至关重要.
研究的目的:
- 分析HTPB推进剂的固化过程.
- 开发和验证HTPB推进剂固化的预测模型.
- 研究加热速度对固化动力学和时间的影响.
主要方法:
- 使用差分扫描热量计 (DSC) 来收集不同加热速率的实验反应数据.
- 开发了一个热化学模型来描述反应动力学.
- 使用有限元模型来模拟温度和固化度的时空演变.
主要成果:
- 来自DSC的实验数据为固化过程提供了关键反应参数.
- 开发的模型准确地模拟了HTPB推进剂固化过程中的温度和固化度演变.
- 模拟表明,加热速度的增加显著加快了固化反应,从而减少了整体固化时间.
结论:
- 该研究成功验证了HTPB推进剂固化的计算模型.
- 这些发现证实,优化加热速度是减少HTPB推进剂处理时间的关键因素.
- 未来的研究应该纳入额外的变量,如材料杂质和复杂的条件,以提高模型的准确性和实际应用.
更多相关视频
相关概念视频
Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control
2.9K
The addition of a hydrogen halide to 1,3-butadiene gives a mixture of 1,2- and 1,4-adducts. Since more substituted alkenes are more stable, the 1,4-adduct is expected to be the major product. However, the product distribution is strongly influenced by temperature; low temperature favors the 1,2-adduct, whereas the 1,4-adduct is predominant at high temperature.
2.9K
Free-Radical Chain Reaction and Polymerization of Alkenes
8.2K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
8.2K
Cationic Chain-Growth Polymerization: Mechanism
2.4K
The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
2.4K
Step-Growth Polymerization: Overview
3.6K
Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
Many natural and synthetic polymers are produced by...
3.6K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
2.0K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
2.0K
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
8.7K
The rate of acid-catalyzed hydration of alkenes depends on the alkene's structure, as the presence of alkyl substituents at the double bond can significantly influence the rate.
8.7K


