Crystallization behavior, mechanical properties, and environmental biodegradability of poly(?-hydroxybutyrate)/cellulose acetate butyrate blends

2003 ◽  
Vol 89 (8) ◽  
pp. 2116-2122 ◽  
Author(s):  
Tiezhu Wang ◽  
Guoxiang Cheng ◽  
Shihu Ma ◽  
Zhijiang Cai ◽  
Liguang Zhang
Keyword(s):  
Mechanical Properties ◽  
Cellulose Acetate ◽  
Crystallization Behavior ◽  
Cellulose Acetate Butyrate ◽  
Acetate Butyrate

Cellulose acetate butyrate/poly(caprolactonetriol) blends: Miscibility, mechanical properties, and in vivo inflammatory response

2014 ◽  
Vol 29 (5) ◽  
pp. 654-661 ◽  
Author(s):  
Luiz A Kanis ◽  
Ellen L Marques ◽  
Karine M Zepon ◽  
Jefferson R Pereira ◽  
Saulo Pamato ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Hydrogen Bonding ◽  
Inflammatory Response ◽  
Cellulose Acetate ◽  
Intramolecular Hydrogen Bonding ◽  
Cellulose Acetate Butyrate ◽  
Swelling Capacity ◽  
Intramolecular Hydrogen ◽  
Acetate Butyrate

This study reports the results of the characterization of cellulose acetate butyrate and polycaprolactone-triol blends in terms of miscibility, swelling capacity, mechanical properties, and inflammatory response in vivo. The cellulose acetate butyrate film was opaque and rigid, with glass transition ( T g) at 134℃ and melting temperature of 156℃. The cellulose acetate butyrate/polycaprolactone-triol films were transparent up to a polycaprolactone-triol content of 60%. T g of the cellulose acetate butyrate films decreased monotonically as polycaprolactone-triol was added to the blend, thus indicating miscibility. FTIR spectroscopy revealed a decrease in intramolecular hydrogen bonding in polycaprolactone-triol, whereas no hydrogen bonding was observed between cellulose acetate butyrate and –OH from polycaprolactone-triol. The increase in polycaprolactone-triol content in the blend decreased the water uptake. An increase in polycaprolactone-triol content decreased the modulus of elasticity and increased the elongation at break. A cellulose acetate butyrate/polycaprolactone-triol 70/30 blend implanted in rats showed only an acute inflammatory response 7 days after surgery. No change in inflammation mediators was observed.

scholarly journals Study on Cellulose Acetate Butyrate/Plasticizer Systems by Molecular Dynamics Simulation and Experimental Characterization

Polymers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1272
Author(s):  
Weizhe Wang ◽  
Lijie Li ◽  
Shaohua Jin ◽  
Yalun Wang ◽  
Guanchao Lan ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Molecular Dynamics ◽  
Molecular Dynamics Simulation ◽  
Cellulose Acetate ◽  
Distribution Functions ◽  
Binding Energies ◽  
Cellulose Acetate Butyrate ◽  
Dynamics Simulation ◽  
Solubility Parameters ◽  
Acetate Butyrate

Cellulose acetate butyrate (CAB) is a widely used binder in polymer bonded explosives (PBXs). However, the mechanical properties of PBXs bonded with CAB are usually very poor, which makes the charge edges prone to crack. In the current study, seven plasticizers, including bis (2,2-dinitro propyl) formal/acetal (BDNPF/A or A3, which is 1:1 mixture of the two components), azide-terminated glycidyl azide (GAPA), n-butyl-N-(2-nitroxy-ethyl) nitramine (Bu-NENA), ethylene glycol bis(azidoacetate) (EGBAA), diethylene glycol bis(azidoacetate) (DEGBAA), trimethylol nitromethane tris (azidoacetate) (TMNTA) and pentaerythritol tetrakis (azidoacetate) [PETKAA], were studied for the plasticization of CAB. Molecular dynamics simulation was conducted to distinguish the compatibilities between CAB and plasticizers and to predict the mechanical properties of CAB/plasticizer systems. Considering the solubility parameters, binding energies and intermolecular radical distribution functions of these CAB/plasticizer systems comprehensively, we found A3, Bu-NENA, DEGBAA and GAPA are compatible with CAB. The elastic moduli of CAB/plasticizer systems follow the order of CAB/Bu-NENA>CAB/A3>CAB/DEGBAA>CAB/GAPA, and their processing property is in the order of CAB/Bu-NENA>CAB/GAPA>CAB/A3>CAB/DEGBAA. Afterwards, all the systems were characterized by FT-IR, differential scanning calorimetry (DSC), differential thermogravimetric analysis (DTA) and tensile tests. The results suggest A3, GAPA and Bu-NENA are compatible with CAB. The tensile strengths and Young’s moduli of these systems are in the order of CAB/A3>CAB/Bu-NENA>CAB/GAPA, while the strain at break of CAB/Bu-NENA is best, which are consistent with simulation results. Based on these results, it can be concluded that A3, Bu-NENA and GAPA are the most suitable plasticizers for CAB binder in improving mechanical and processing properties. Our work has provided a crucial guidance for the formulation design of PBXs with CAB binder.

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