TY - JOUR
T1 - Hydroxyl-terminated polybutadiene(HTPB) propellants cross-linked by dimer acid diisocyanate (DDI)
T2 - Cross-linking network and properties
AU - Xin, Kai
AU - Yang, Rongjie
AU - Yang, Kairui
AU - Li, Jianmin
AU - Zhai, Jinxian
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024
Y1 - 2024
N2 - Considering the high toxicity of toluene diisocyanate (TDI) and the low reactivity of isophorone diisocyanate (IPDI), a low-toxicity curing agent, dimer acid diisocyanate (DDI), was used to cross-link HTPB elastomers and propellants. The unique long-chain structure of DDI not only ensures the elastic modulus and tensile strength of the elastomer, but also improves the flexibility to some extent. The long flexible chains promote the segment movement, which is very important for the formation of hydrogen bonds between segments. The chemical cross-linking network and hydrogen bonding association play a significant role in the mechanical properties of the HTPB/DDI system. The relationship between the mole ratio of -NCO to -OH (R-value) and the mechanical properties of HTPB/DDI elastomers were also investigated. In the range of R-value from 0.85 to 1.2, the elastic modulus and tensile strength first increase and then decrease, and the elongation at break first decreases and then increases. Under the same curing conditions, the elastic modulus and tensile strength of the HTPB/DDI propellant are similar to the HTPB/TDI propellant. For the HTPB/AP/Al propellants and HTPB/AP/RDX/Al propellants, the HTPB/DDI system has lower burning rates in the range of 5–19 MPa than the HTPB/TDI system and HTPB/IPDI system. The application of DDI can reduce the burning rates of the propellant without adding any burning rate modifiers. It is considered that DDI can replace TDI and IPDI as a new curing agent with low toxicity and moderate reactivity for HTPB systems.
AB - Considering the high toxicity of toluene diisocyanate (TDI) and the low reactivity of isophorone diisocyanate (IPDI), a low-toxicity curing agent, dimer acid diisocyanate (DDI), was used to cross-link HTPB elastomers and propellants. The unique long-chain structure of DDI not only ensures the elastic modulus and tensile strength of the elastomer, but also improves the flexibility to some extent. The long flexible chains promote the segment movement, which is very important for the formation of hydrogen bonds between segments. The chemical cross-linking network and hydrogen bonding association play a significant role in the mechanical properties of the HTPB/DDI system. The relationship between the mole ratio of -NCO to -OH (R-value) and the mechanical properties of HTPB/DDI elastomers were also investigated. In the range of R-value from 0.85 to 1.2, the elastic modulus and tensile strength first increase and then decrease, and the elongation at break first decreases and then increases. Under the same curing conditions, the elastic modulus and tensile strength of the HTPB/DDI propellant are similar to the HTPB/TDI propellant. For the HTPB/AP/Al propellants and HTPB/AP/RDX/Al propellants, the HTPB/DDI system has lower burning rates in the range of 5–19 MPa than the HTPB/TDI system and HTPB/IPDI system. The application of DDI can reduce the burning rates of the propellant without adding any burning rate modifiers. It is considered that DDI can replace TDI and IPDI as a new curing agent with low toxicity and moderate reactivity for HTPB systems.
KW - combustion
KW - cross-linking network
KW - dimer acid diisocyanate
KW - hydroxyl-terminated polybutadiene
KW - propellants
UR - http://www.scopus.com/inward/record.url?scp=85192930474&partnerID=8YFLogxK
U2 - 10.1002/prep.202300259
DO - 10.1002/prep.202300259
M3 - Article
AN - SCOPUS:85192930474
SN - 0721-3115
JO - Propellants, Explosives, Pyrotechnics
JF - Propellants, Explosives, Pyrotechnics
ER -