New Insightl into the Structure-Property Relationships of Hybrid (Inorganic/Organic) Poss™ Thermoplastics

2000 ◽  
Vol 628 ◽  
Author(s):  
Shawn H. Phillips ◽  
Rusty L. Blanski ◽  
Steven A. Svejda ◽  
Timothy S. Haddad ◽  
Andre Lee ◽  
...  

The demand for multi-purpose, high-performance polymer systems has resulted in a need for advancing polymer properties beyond what traditional systems can offer. Only through control/alteration at the molecular level can one maximize property enhancements to meet current military and commercial needs. Over the last seven years the Air Force Research Laboratory has developed and incorporated discrete Si-O frameworks (POSS = Polyhedral Oligomeric Silsesquioxanes) into traditional organic polymer systems. This research has resulted in new hybrid inorganic-organic polymer systems with remarkable enhancements in mechanical and physical properties including dramatic increases in both glass transition and decomposition temperatures, reduced flammability, increased moduli and oxidation resistance. We have shown that these enhancements result from the chemical composition (Si-O core) and size (∼15 A in diameter) of the POSS frameworks, and can be copolymerized, grafted, or even blended using traditional processing methods. Recently, we have focused our efforts on understanding and controlling the molecular level interactions between POSS frameworks and the polymer matrix. The development of new POSS monomers has allowed us to study how functionality, size, and geometry enhances the bulk properties of these hybrid materials. For example, increasing the solubility of side groups on the POSS framework results in greater POSS-polymer matrix interactions and increased Tg and storage moduli. Recent studies with POSS blends have resulted in increases in hardness, and reductions in dielectric constants and coefficients of thermal expansion. New results in polymer synthesis, characterization, and applications will be discussed with a strong emphasis on the versatility of this new nanotechnology to many polymer systems.

Author(s):  
J. Petermann ◽  
G. Broza ◽  
U. Rieck ◽  
A. Jaballah ◽  
A. Kawaguchi

Oriented overgrowth of polymer materials onto ionic crystals is well known and recently it was demonstrated that this epitaxial crystallisation can also occur in polymer/polymer systems, under certain conditions. The morphologies and the resulting physical properties of such systems will be presented, especially the influence of epitaxial interfaces on the adhesion of polymer laminates and the mechanical properties of epitaxially crystallized sandwiched layers.Materials used were polyethylene, PE, Lupolen 6021 DX (HDPE) and 1810 D (LDPE) from BASF AG; polypropylene, PP, (PPN) provided by Höchst AG and polybutene-1, PB-1, Vestolen BT from Chemische Werke Hüls. Thin oriented films were prepared according to the method of Petermann and Gohil, by winding up two different polymer films from two separately heated glass-plates simultaneously with the help of a motor driven cylinder. One double layer was used for TEM investigations, while about 1000 sandwiched layers were taken for mechanical tests.


Author(s):  
Barbara A. Wood

A controversial topic in the study of structure-property relationships of toughened polymer systems is the internal cavitation of toughener particles resulting from damage on impact or tensile deformation.Detailed observations of the influence of morphological characteristics such as particle size distribution on deformation mechanisms such as shear yield and cavitation could provide valuable guidance for selection of processing conditions, but TEM observation of damaged zones presents some experimental difficulties.Previously published TEM images of impact fractured toughened nylon show holes but contrast between matrix and toughener is lacking; other systems investigated have clearly shown cavitated impact modifier particles. In rubber toughened nylon, the physical characteristics of cavitated material differ from undamaged material to the extent that sectioning of heavily damaged regions by cryoultramicrotomy with a diamond knife results in sections of greater than optimum thickness (Figure 1). The detailed morphology is obscured despite selective staining of the rubber phase using the ruthenium trichloride route to ruthenium tetroxide.


Author(s):  
W.W. Adams ◽  
S. J. Krause

Rigid-rod polymers such as PBO, poly(paraphenylene benzobisoxazole), Figure 1a, are now in commercial development for use as high-performance fibers and for reinforcement at the molecular level in molecular composites. Spinning of liquid crystalline polyphosphoric acid solutions of PBO, followed by washing, drying, and tension heat treatment produces fibers which have the following properties: density of 1.59 g/cm3; tensile strength of 820 kpsi; tensile modulus of 52 Mpsi; compressive strength of 50 kpsi; they are electrically insulating; they do not absorb moisture; and they are insensitive to radiation, including ultraviolet. Since the chain modulus of PBO is estimated to be 730 GPa, the high stiffness also affords the opportunity to reinforce a flexible coil polymer at the molecular level, in analogy to a chopped fiber reinforced composite. The objectives of the molecular composite concept are to eliminate the thermal expansion coefficient mismatch between the fiber and the matrix, as occurs in conventional composites, to eliminate the interface between the fiber and the matrix, and, hopefully, to obtain synergistic effects from the exceptional stiffness of the rigid-rod molecule. These expectations have been confirmed in the case of blending rigid-rod PBZT, poly(paraphenylene benzobisthiazole), Figure 1b, with stiff-chain ABPBI, poly 2,5(6) benzimidazole, Fig. 1c A film with 30% PBZT/70% ABPBI had tensile strength 190 kpsi and tensile modulus of 13 Mpsi when solution spun from a 3% methane sulfonic acid solution into a film. The modulus, as predicted by rule of mixtures, for a film with this composition and with planar isotropic orientation, should be 16 Mpsi. The experimental value is 80% of the theoretical value indicating that the concept of a molecular composite is valid.


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1811
Author(s):  
Valeriia Rostovtseva ◽  
Alexandra Pulyalina ◽  
Roman Dubovenko ◽  
Ilya Faykov ◽  
Kseniya Subbotina ◽  
...  

Modification of polymer matrix by hybrid fillers is a promising way to produce membranes with excellent separation efficiency due to variations in membrane structure. High-performance membranes for the pervaporation dehydration were produced by modifying poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) to facilitate lactic acid purification. Ionic liquid (IL), heteroarm star macromolecules (HSM), and their combination (IL:HSM) were employed as additives to the polymer matrix. The composition and structure of hybrid membranes were characterized by X-ray diffraction and FTIR spectroscopy. Scanning electron microscopy was used to investigate the membranes surface and cross-section morphology. It was established that the inclusion of modifiers in the polymer matrix leads to the change of membrane structure. The influence of IL:HSM was also studied via sorption experiments and pervaporation of water‒lactic acid mixtures. Lactic acid is an essential compound in many industries, including food, pharmaceutical, chemical, while the recovering and purifying account for approximately 50% of its production cost. It was found that the membranes selectively remove water from the feed. Quantum mechanical calculations determine the favorable interactions between various membrane components and the liquid mixture. With IL:HSM addition, the separation factor and performance in lactic acid dehydration were improved compared with pure polymer membrane. The best performance was found for (HSM: IL)-PPO/UPM composite membrane, where the permeate flux and the separation factor of about 0.06 kg m−2 h−1 and 749, respectively, were obtained. The research results demonstrated that ionic liquids in combination with star macromolecules for membrane modification could be a promising approach for membrane design.


Cellulose ◽  
2021 ◽  
Author(s):  
Koki Matsumoto ◽  
Tatsuya Tanaka ◽  
Masahiro Sasada ◽  
Noriyuki Sano ◽  
Kenta Masuyama

AbstractThis study focused on realizing fire retardancy for polymer composites by using a cellulosic biofiller and ammonium polyphosphate (APP). The motivation of this study was based on revealing the mechanism of the synergetic effect of a cellulosic biofiller and APP and determining the parameters required for achieving a V-0 rating in UL94 standard regardless of the kind of polymer system used. As for the polymer matrix, polypropylene and polylactic acid were used. The flammability, burning behavior and thermal decomposition behavior of the composites were investigated through a burning test according to the UL-94 standard, cone calorimetric test and thermogravimetric analysis. As a result, the incorporation of a high amount of cellulose enabled a V-0 rating to be achieved with only a small amount of APP despite the variation of the optimum cellulose loading between the matrix polymers. Through analysis, the results indicated that APP decreased the dehydration temperature of cellulose. Furthermore, APP promoted the generation of enough water as a nonflammable gas and formed enough char until the degradation of the polymer matrix was complete. The conditions required to achieve the V-0 rating were suggested against composites incorporating APP and biofillers. Furthermore, the suggested conditions were validated by using polyoxymethylene as a highly flammable polymer.


Author(s):  
Yifeng He ◽  
Man He ◽  
Beibei Chen ◽  
Bin Hu

A novel sulfur-containing functional core-shell magnetic porous organic polymer (Fe3O4@BD-TpMA-S-SH MOPs) was synthesized as magnetic solid phase extraction (MSPE) sorbent for mercury speciation followed by high performance liquid chromatography (HPLC)...


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