Synthesis of polyimides from α,αʹ-bis(3-aminophenoxy)-p-xylene: Spectroscopic, single crystal XRD and thermal studies

The final publication is available at Elsevier via http://dx.doi.org/10.1016/j.molstruc.2018.01.098 © 2018. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/The meta-catenated ether-based diamine monomer α,αʹ-bis(3-aminophenoxy)-p-xylene (3APX) was synthesized from dinitro precursor α,αʹ-bis(3-nitrophenoxy)-p-xylene (3NPX). FTIR, 1H and 13C NMR spectroscopic studies accompanied by elemental analysis were performed for structural elucidations of 3NPX and 3APX. The spatial orientations of 3APX were explored by single crystal X-ray diffraction analysis. Its crystal system was found to be monoclinic, adopting the space group P21/c. The synthesized diamine monomer (3APX) was used for preparation of new series of polyimides by reacting with three different dianhydrides (BTDA, ODPA, 6FDA). The relevant copolyimides were developed via incorporation of 4,4ʹ-methylenedianiline (MDA) in the backbone of afore-synthesized polyimides. The structures of polyimides and copolyimides were verified by FTIR and 1H NMR spectroscopic techniques. Their properties were evaluated by dynamic and isothermal TGA (nitrogen and air atmospheres) and WAXRD studies. Polyimides displayed significantly high thermal stability as their degradation started around 400 °C and it was improved further by execution of copolymerization strategy with MDA. The 5% weight loss temperature (T5) of polyimides under nitrogen atmosphere was in the range of 425–460 °C while for copolyimides it increased to 454–498 °C. Thermal decomposition in air was slower than nitrogen between 400 and 550 °C however it was accelerated above 550 °C. Isothermal TGA disclosed that copolyimides have the ability to endure elevated temperatures for extended period. WAXRD analysis showed the amorphous nature of polyimides and copolyimides.Indigenous 5000 Ph.D. Fellowship Program (Phase II)International Research Support Initiative Program (IRSIP)Quaid-i-Azam University, Pakistan under University Research Fund (URF)University of Waterloo, Canada under Natural Sciences and Engineering Research Council of Canada (NSERC) Discovery Gran

Structural Framework for Flight: NASA's Role in Development of Advanced Composite Materials for Aircraft and Space Structures

This serves as a source of collated information on Composite Research over the past four decades at NASA Langley Research Center, and is a key reference for readers wishing to grasp the underlying principles and challenges associated with developing and applying advanced composite materials to new aerospace vehicle concepts. Second, it identifies the major obstacles encountered in developing and applying composites on advanced flight vehicles, as well as lessons learned in overcoming these obstacles. Third, it points out current barriers and challenges to further application of composites on future vehicles. This is extremely valuable for steering research in the future, when new breakthroughs in materials or processing science may eliminate/minimize some of the barriers that have traditionally blocked the expanded application of composite to new structural or revolutionary vehicle concepts. Finally, a review of past work and identification of future challenges will hopefully inspire new research opportunities and development of revolutionary materials and structural concepts to revolutionize future flight vehicles

High Temperature Polymer Matrix Composites

These are the proceedings of the High Temperature Polymer Matrix Composites Conference held at the NASA Lewis Research Center on March 16 to 18, 1983. The purpose of the conference is to provide scientists and engineers working in the field of high temperature polymer matrix composites an opportunity to review, exchange, and assess the latest developments in this rapidly expanding area of materials technology. Technical papers are presented in the following areas: (1) matrix development; (2) adhesive development; (3) characterization; (4) environmental effects; and (5) applications

Processing and characterization of nanocomposites prepared by high torque melt mixing, 2017

The rapid development of polymer nanocomposites has received extensive attention over the last few decades. The ability to alter functionalities of composites, dramatically improving properties and performance at low filler content creates flexibility in designing materials for advanced applications in various industrial fields. This work focuses on nanocomposites relevant to the packaging and aerospace industries. This work evaluated the ability to homogeneously distribute nanomaterials into a polymer matrix, understand the effects on rheological properties, understand changes to microstructure and effects, and characterize properties of resulting nanocomposite. High torque melt mixing was used to disperse surface modified cellulose nanocrystals in a poly(lactic acid) (PLA) resin and graphene in a phenylethynyl terminated imide resin, PETI 298, using bulk graphite. Rheology, Raman spectroscopy, and X-Ray powder diffraction were applied for the understanding of changes to the microstructure and location of optimum loading by the determination of the percolation threshold. Thermomechanical performance was evaluated through TGA, DMA, and DSC. It was determined that graphene and short stacks of graphene could be dispersed and distributed at low loadings in PETI 298. As expected, the addition of graphitic material led to an increase in viscosity, but also caused a retardation of the cure which could be attributed to increased viscosity or quenching of free radicals. Changes to the microstructure were difficult to evaluate because of the competing chemistry occurring in the system but it could be determined that something significant occurs around 1 wt % at which the melt rheology and the microstructure behavior was different from other composites. It was further determined that the melt mixing process led to the formation of an ordered structured. Modification of the cellulose nanocrystals (m-CNC) with Cardura, glycidyl ester, provided no improvement to mechanical properties of PLA composites. However, m-CNCs were found to nucleate the crystallization of PLA. Lack of improvement to mechanical properties could be attributed to the degradation of polymer during processing. KEY TERMS: Nanocomposite, Polyimide, Graphite, Cellulose, Lactide, Chemistry, Materials Chemistry, Polymer Chemistr

40th Rocky Mountain Conference on Analytical Chemistry

Final program, abstracts, and information about the 40th annual meeting of the Rocky Mountain Conference on Analytical Chemistry, co-sponsored by the Colorado Section of the American Chemical Society and the Rocky Mountain Section of the Society for Applied Spectroscopy. Held in Denver, Colorado, July 25 - August 1, 1998

Advanced Materials Technology

Composites, polymer science, metallic materials (aluminum, titanium, and superalloys), materials processing technology, materials durability in the aerospace environment, ceramics, fatigue and fracture mechanics, tribology, and nondestructive evaluation (NDE) are discussed. Research and development activities are introduced to the nonaerospace industry. In order to provide a convenient means to help transfer aerospace technology to the commercial mainstream in a systematic manner

Developing complexity using networks of synthetic replicators

Molecular recognition plays an essential role in the self-assembly and self-organisation of biological and chemical systems alike—allowing individual components to form complex interconnected networks. Within these systems, the nature of the recognition and reactive processes determines their functional and structural properties, and even small changes in their identity or orientation can exert a dramatic effect on the observed properties. The rapidly developing field of systems chemistry aims to move away from the established paradigm in which molecules are studied in isolation, towards the study of networks of molecules that interact and react with each other. Taking inspiration from complex natural systems, where recognition processes never operate in isolation, systems chemistry aims to study chemical networks with the view to examining the system-level properties that arise from the interactions and reactions between the components within these systems. The work presented in this thesis aims to advance the nascent field of systems chemistry by bringing together small organic molecules that can react and interact together to form interconnected networks, exhibiting complex behaviour, such as self-replication, as a result. Three simple building blocks are used to construct a network of two structurally similar replicators and their kinetic behaviour is probed through a comprehensive kinetic analysis. The selectivity for one of the recognition-mediated reactive processes over another is examined within the network in isolation as well as in a scenario where the network is embedded within a pool of exchanging components. The interconnected, two-replicator network is examined under far-from-equilibrium reaction-diffusion conditions, showing that chemical replicating networks can exhibit signs of selective replication—a complex phenomenon normally associated with biological systems. Finally, a design of a well-characterised replicator is exploited for the construction of a network integrating self-replication with a another recognition-directed process, leading to the formation of a mechanically-interlocked architecture—a [2]rotaxane.EPSRC grant EP/K503162/1 (DTG012)Funded by EPSRC grant EP/K503162/1 (DTG012

Development of Photo-Affinity based ROMP Polymers for Identifying Receptors on Cell Surface

Chapter 1 Receptors on cell membrane surfaces play critical roles for the cell to communicate with the outside environment by forming protein complexes. Therefore, identifying protein partners in the complex is of major importance. We are developed ROMP (ring opening metasthesis polymerization) polymers as tools for identifying the partners. The polymers bear several functional groups such as ligands for binding to a known receptor, benzophenone group to covalently connect the partner proteins to the polymer, and alkyne for click reaction to attach biotins. With this functionalized polymer, possible protein partners can be purified and analyzed by peptide mass finger printing. To optimize the function of this polymer and the experimental procedure, the α vβ 3-MMP2, was used as a model system. Chapter 4 A new prodrug for selective cancer therapy that uses the increased activities of histone deacetylase (HDAC) and protease cathepsin L (CTSL) in cancer cells was synthesized. Puromycine coupled with acetylated lysine group is not cytotoxic because the free amine is masked. We optimized the synthesis and the purification of puromycine coupled with acetylated lysine group to obtain highly pure (\u3c95 %) product for testing in vivo. Chapter 5 Early diagnosis of metastasis and prevention of metastasis is a major obstacle in cancer treatment due to the lack of imaging probes specific to early stage cancer. MT1-MMP, a membrane anchored matrix metalloproteinase, is upregulated in invasive human breast cancers even in early stages. The PEX domain of MT1-MMP is required for migration of aggressive cancer cells.Peptides mimicking 8 amino acids of the outermost β -strand of the blades from the PEX domain of MT1-MMP successfully inhibited the migration of aggressive cancer cells. This peptide was coupled to 18F-FDG for PET imaging and testing of the conjugate in vitro and in vivo. | 216 page