RESUMEN
The crystal moisture sensitivity can be tuned by the chemical composition on the crystal surface. Ammonium dinitramide (ADN) crystal is a promising oxidizer for solid propellants. However, its strong moisture sensitivity greatly limits its practical applications. Here, we report a novel strategy to reduce moisture sensitivity by trapping ammonium cations with montmorillonite (MMT) to modulate the chemistry composition on the ADN crystal surface. An extraordinary phenomenon can be found: the crystal surface of the recrystallized ADN with 1% MMT (ADN-1% MMT) is rearranged with more low-surface-energy -NO2 groups (65.84%) and less high-surface-energy NH4+ groups (4.8%). In addition, ADN-1% MMT presents a more homogeneous low surface energy feature with a narrower surface energy distribution. As a result, ADN-1% MMT exhibits a noticeably lower hygroscopicity at 20 °C and 60% RH, which is accordant with the simulated hygroscopicity based on XRD and moisture sensitivity prediction based on surface energy. This study brings out a novel modification idea to adjust crystal moisture sensitivity by tuning the chemistry composition on the crystal surface based on trapping cations.
RESUMEN
To improve the mechanical properties of polyurethane cross-linked poly (ethylene oxide-co-tetrahydrofuran) (P(E-co-T)) elastomers at room temperature, using poly (ethylene oxide-co-tetrahydrofuran) and high-molecular-weight polyethylene glycol (PEG) as raw materials and polyisocyanate N100 as curing agent, a series of polyurethane cross-linked blended polyether elastomers were prepared by changing the elastomer-curing parameter R value (n(-NCO)/n(-OH)) and P(E-co-T)/PEG ratio. Equilibrium swelling measurements showed that the chemical cross-linkage of the elastomers tended to decrease with the decreasing R value, the average molecular weight (Mc) of the network chain increased, and the density of the network chain (N0) decreased. Wide-angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC) tests showed that PEG chain segments within the elastomers crystallized at room temperature, while the crystallinity increased with decreasing R value and increasing PEG content. The mechanical property tests showed that the elongation at break tended to decrease with increasing R value; the tensile strength first increased and then decreased. At R value 0.9, the elastomer presented good comprehensive mechanical properties. In addition, the mechanical properties of polyurethane cross-linked P(E-co-T)/PEG blended polyether elastomer showed an increasing trend with the increase in PEG content when the curing parameter of 0.9 remained unchanged.
RESUMEN
Propargyl terminal Polybutadiene (PTPB) was successfully prepared through hydroxyl terminal polybutadiene (HTPB) end-capping modification. The FTIR and 13C NMR results indicated that the HTPB terminal hydroxyl was thoroughly replaced and yielded the target product, PTPB, with a theoretical propargyl content of 0.66 mmol g-1. In comparison with HTPB, PTPB has a lower viscosity. Using 1,6-diazide hexane as a curing agent, polytriazole crosslinked polybutadiene (PTriPB) elastomers with various functional molar ratios (R) were prepared by CuAAC reaction, and the glass transition temperatures of the resultant PTriPB elastomers were approximately -75 °C, measured by differential scanning calorimetry (DSC), nearly independent of elastomer R values. Mechanical tests indicated, that with the increase in R, the mechanical properties of PTriPB elastomers exhibit a parabolic dependence on R. In addition, the thermal stability of PTriPB elastomers were also studied. The findings revealed some fundamental features of polytriazole crosslinking elastomer prepared by CuAAC reaction.
RESUMEN
The relationship between temperature and the mechanical properties of an end cross-linked equal molar random copolyether elastomer of 3,3-bis(azidomethyl)oxetane and tetrahydrofuran (P(BAMO-r-THF)) was investigated. During this investigation, the performances of two P(BAMO-r-THF) elastomers with different thermal histories were compared at different temperatures. The elastomer as prepared at 20 °C (denoted as S0) exhibited semi-crystallization morphology. Wide angle X-ray diffraction analysis indicated that the crystal grains within elastomer S0 result from the crystallization of BAMO micro-blocks embedded in P(BAMO-r-THF) polymeric chains, and the crystallinity is temperature irreversible under static conditions. After undergoing a heating-cooling cycle, this elastomer became an amorphous elastomer (denoted as S1). Regarding mechanical properties, at 20 °C, break strains and stresses of 315 ± 22% and 0.46 ± 0.01 MPa were obtained for elastomer S0; corresponding values of 294 ± 6% and 0.32 ± 0.02 MPa were obtained for elastomer S1. At -40 °C, these strains and stresses simultaneously increased to 1085 ± 21% and 8.90 ± 0.72 MPa (S0) and 1181 ± 25% and 10.23 ± 0.44 MPa (S1), respectively, owing to the strain-induced crystallization of BAMO micro-blocks within the P(BAMO-r-THF) polymeric chains.