PAN polyacrylonitrile

PAN is a member of the olefin family. In general, it is somewhat similar to the other olefins such as polyethylene and pol)rpropylene in terms of appearance, general chemical characteristics, and electrical properties. 

PAN has corrosion resistance properties similar to those of pol)/propylene and polyethylene. 

The chemical listed are in the pure state or in a saturated solution unless otherwise indicated. Compatibility is shown to the maximum allowable temperature for which data is available. Incompatibility is shown by an X. A blank space indicates that data is unavailable. 

Source From P.A. Schweitzer. 2004. Corrosion Resistance Tables, Vols. 1-4,5th ed.. New York Marcel Dekker. 

Polyacrylonitrile is used to produce molded appliance parts, automotive parts, garden hose, vending machine tubing, chemical apparatus, typewriter cases, bags, luggage shells, and trim. 

Schindler and Maier [24] were the first researchers involved in the preparation of the PAN carbon membrane based on their US patent issued in 1990. They prepared 

Furthermore, PAN hollow fiber carbon membranes were coated with zeohtes [28], PI [29] and perfluoro-srrlfonated ionomer (PSI) [30] to produce composite membranes. After this period, there was not much research involving the rrse of PAN as a precursor for carbon membranes until late 2003, when Davis and Ismail [31] prepared their carbon hollow fiber membrane from PAN precursor. 

Peak Notation Assignment of Main Peaks Molecular Weight Retention Index Relative Intensity 

AAA2 hexane-1,3,5-tricarbonltrlle (trimer) AAA3 pentane-1,3,5-tricarbonitrile (trimer) 

T2 nona-1,8-diene-2,4,6,8-tetracarbonitrile (tetramer) T3 heptane-1,3,5,7-tetracarbonitrile (tetramer) 

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Polyacrylonitrile (PAN) films have outstanding oxygen and CO2 barrier properties, but only modest water-vapor barrier properties. They are for processed-meat and fresh pasta packaging laminations where an oxygen barrier is required for vacuum or gas flush packaging. 

Process. Any standard precursor material can be used, but the preferred material is wet spun Courtaulds special acrylic fiber (SAF), oxidized by RK Carbon Fibers Co. to form 6K Panox B oxidized polyacrylonitrile (PAN) fiber (OPF). This OPF is treated ia a nitrogen atmosphere at 450—750°C, preferably 525—595°C, to give fibers having between 69—70% C, 19% N density less than 2.5 g/mL and a specific resistivity under 10 ° ohm-cm. If crimp is desired, the fibers are first knit iato a sock before heat treating and then de-knit. Controlled carbonization of precursor filaments results ia a linear Dow fiber (LDF), whereas controlled carbonization of knit precursor fibers results ia a curly carbonaceous fiber (EDF). At higher carbonizing temperatures of 1000—1400°C the fibers become electrically conductive (22). 

Polymer Solvent. Sulfolane is a solvent for a variety of polymers, including polyacrylonitrile (PAN), poly(vinyhdene cyanide), poly(vinyl chloride) (PVC), poly(vinyl fluoride), and polysulfones (124—129). Sulfolane solutions of PAN, poly(vinyhdene cyanide), and PVC have been patented for fiber-spinning processes, in which the relatively low solution viscosity, good thermal stabiUty, and comparatively low solvent toxicity of sulfolane are advantageous. Powdered perfluorocarbon copolymers bearing sulfo or carboxy groups have been prepared by precipitation from sulfolane solution with toluene at temperatures below 300°C. Particle sizes of 0.5—100 p.m result. 

The property of mesophase that makes it suitable for carbon fiber and premium coke manufacture is that it forms ordered stmctures under stress which persist following carbonization. However, most carbon fiber production in the 1990s is based on polyacrylonitrile (PAN). 

Heterogeneous polymerization is characteristic of a number of monomers, including vinyl chloride and acrylonitrile. A completely satisfactory mechanism for these reactions has not been deterrnined. This is tme for VDC also. Earlier studies have not been broad enough to elucidate the mechanism (26,30,31). Morphologies of as-polymerized poly(vinyl chloride) (PVC) and polyacrylonitrile (PAN) are similar, suggesting a similar mechanism. 

More than 95% of current carbon fiber production for advanced composite appHcations is based on the thermal conversion of polyacrylonitrile (PAN) or pitch precursors to carbon or graphite fibers. Generally, the conversion of PAN or pitch precursor to carbon fiber involves similar process steps fiber formation, ie, spinning, stabilization to thermoset the fiber, carbonization—graphitization, surface treatment, and sizing. Schematic process flow diagrams are shown in Eigure 4. However, specific process details differ. 

Because of their unique blend of properties, composites reinforced with high performance carbon fibers find use in many structural applications. However, it is possible to produce carbon fibers with very different properties, depending on the precursor used and processing conditions employed. Commercially, continuous high performance carbon fibers currently are formed from two precursor fibers, polyacrylonitrile (PAN) and mesophase pitch. The PAN-based carbon fiber dominates the ultra-high strength, high temperature fiber market (and represents about 90% of the total carbon fiber production), while the mesophase pitch fibers can achieve stiffnesses and thermal conductivities unsurpassed by any other continuous fiber. This chapter compares the processes, structures, and properties of these two classes of fibers. 

Low density, carbon fiber-carbon binder composites are fabricated from a variety of carbon fibers, including fibers derived from rayon, polyacrylonitrile (PAN), isotropic pitch, and mesophase pitch. The manufacture, structure, and properties of carbon fibers have been thoroughly reviewed elsewhere [3] and. therefore, are... 

On the other hand, organic materials of relatively low molecular weight such as acetylene, benzene, ethylene and methane, can produce vapour-grown carbon materials by imperfect combustion or by exposing their vapour to a heated substrate in an electric furnace in the presence of a metal catalyst. The latter process generates VGCFs. Other precursors to VGCF include polyacrylonitrile (PAN), isotropic or mesophase pitch, rayon or nylon [8]. 

The initial radicals formed from the Ce(IV) ion redox system can initiate a monomer to polymerize and form an end group of the resulting polymer. When the reductant exhibits a carbonyl group, the amide group can be conveniently detected by the FT-IR spectrum of the polymer, such as polyacrylonitrile (PAN). The FT-... 

The final important form of carbon is the carbon fibre formed from polyacrylonitrile (PAN), cellulose or pitch and which is finding increasing ase in fibre-teinfbrced Composites. The corrosion of carbon fibril in composites designed for use under high temperature conditions is currently a severe limitation on their use. 

Acrylonitrile Polyacrylonitrile (PAN) Rugs Orion and Acrilan are copolymers with other monomers... 

The interfacial properties of gel electrolytes containing ethylene carbonate immobilized in a polyacrylonitrile (PAN) matrix with a lithium (bis)trifluoromethane sulfonimide (LiTFSI) salt have been studied 1139]. SEI stability appeared to be strongly dependent on the LiTFSI concentration. A minimum value of / SE1 of about 1000 Qcm2 was obtained after 200h... 

The second group includes SAHs obtained by radical grafting of acrylonitrile (AN) on natural polymers, mostly starch, under the action of cerium initiators [43 -46, 50, 51], The proper crosslinked hydrophilic polymer is formed at the stage of alkali hydrolysis of grafted polyacrylonitrile (PAN), the final characteristics depending on many factors, in particular the sort of starch [46], the methods of its preparation [51], the component ratio, etc. The nature of starch is exhibited through... 

There are two pathways for the degradation of nitriles (a) direct formation of carboxylic acids by the activity of a nitrilase, for example, in Bacillus sp. strain OxB-1 and P. syringae B728a (b) hydration to amides followed by hydrolysis, for example, in P. chlororaphis (Oinuma et al. 2003). The monomer acrylonitrile occurs in wastewater from the production of polyacrylonitrile (PAN), and is hydrolyzed by bacteria to acrylate by the combined activity of a nitrilase (hydratase) and an amidase. Acrylate is then degraded by hydration to either lactate or P-hydroxypropionate. The nitrilase or amidase is also capable of hydrolyzing the nitrile group in a number of other nitriles (Robertson et al. 2004) including PAN (Tauber et al. 2000). 

Recently, nitrilases have been applied to polymer modification, specifically to the modification of polyacrylonitrile (PAN). Nearly 3 x 106 tons of PAN are produced per annum and used in the textile industry. However, there is a great need to improve moisture uptake, dyeability with ionic dyes, and feel of this acrylic fiber. The cyano moieties of PAN have been successfully modified to carboxylates with the commercial Cyanovacta nitrilase, thus enhancing the aforementioned properties of PAN [98]. Nitrilase action on the acrylic fabric was improved... 

In this work, MWNTs will be mixed with polyacrylonitrile (PAN) and the MWNTs/PAN composite will be carbonized, giving rise to a new C/C composite with interesting capacitance properties. It is striking that the composite components alone give negligible capacitance values below 20... 

The high purity carbon nanotubes (CNTs) used in this study were obtained by decomposition of acetylene over a powdered CoxMgi xO solid solution catalyst [19]. Different proportions of CNTs from 15 to 70% and polyacrylonitrile (PAN, Aldrich) have been mixed in an excess of acetone to obtain a slurry. After evaporation of acetone, precursor electrodes were formed by pressing the CNTs/PAN mixture at 1-2 tons/cm2. The C/C composites were formed by carbonisation of the pellets at 700-900°C for 30-420 min under nitrogen flow [20], The optimal capacitance properties of the composite were obtained for a mixture CNTs/PAN (30/70 wt%) treated at 700°C. Such C/C composite remains still quite rich in nitrogen (9 at% of N) demonstrating that PAN is an efficient nitrogen carrier. On the other hand,... 

Polyacrylonitrile (PAN) cloth with surface density of 1.0 kg/m2 and thickness of 10 mm was utilized as the raw material for making ion-exchange sorbents. 

PAN-based carbon fiber processing flow chart, 26 731. See also Polyacrylonitrile (PAN)... 

In practical application, it was reported that the platinum particles dispersed in highly porous carbonized polyacrylonitrile (PAN) microcellular foam used as fuel-cell electrocatalyst160 have the partially active property. The fractal dimension of the platinum particles was determined to be smaller than 2.0 by using the potentiostatic current transient technique in oxygen-saturated solutions, and it was considered to be a reaction dimension, indicating that not all of the platinum particle surface sites are accessible to the incoming oxygen molecules. 

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