Influence Of Polymer Composition Research Articles

The Influence of Polymer Composition on the Hydrolytic and Enzymatic Degradation of Polyesters and Their Block Copolymers with PDMAEMA.

Well-defined, semi-degradable polyester/polymethacrylate block copolymers, based on ε-caprolactone (CL), d,l-lactide (DLLA), glycolide (GA) and N,N′-dimethylaminoethyl methacrylate (DMAEMA), were synthesized by ring-opening polymerization (ROP) and atom transfer radical polymerization. Comprehensive degradation studies of poly(ε-caprolactone)-block-poly(N,N′-dimethylaminoethyl methacrylate) (PCL-b-PDMAEMA) on hydrolytic degradation and enzymatic degradation were performed, and those results were compared with the corresponding aliphatic polyester (PCL). The solution pH did not affect the hydrolytic degradation rate of PCL (a 3% Mn loss after six weeks). The presence of a PDMAEMA component in the copolymer chain increased the hydrolysis rates and depended on the solution pH, as PCL-b-PDMAEMA degraded faster in an acidic environment (36% Mn loss determined) than in a slightly alkaline environment (27% Mn loss). Enzymatic degradation of PCL-b-PDMAEMA, poly(d,l-lactide)-block-poly(N,N′-dimethylaminoethyl methacrylate) (PLA-b-PDMAEMA) and poly(lactide-co-glycolide-co-ε-caprolactone)-block-poly(N,N′-dimethylaminoethyl methacrylate) (PLGC-b-PDMAEMA) and the corresponding aliphatic polyesters (PCL, PLA and PLGC) was performed by Novozyme 435. In enzymatic degradation, PLGC degraded almost completely after eleven days. For polyester-b-PDMAEMA copolymers, enzymatic degradation primarily involved the ester bonds in PDMAEMA side chains, and the rate of polyester degradation decreased with the increase in the chain length of PDMAEMA. Amphiphilic copolymers might be used for biomaterials with long-term or midterm applications such as nanoscale drug delivery systems with tunable degradation kinetics.

Influence of Polymer Composition on the Controlled Release of Docetaxel: A Comparison of Non-Degradable Polymer Films for Oesophageal Drug-Eluting Stents.

Following the huge clinical success of drug-eluting vascular stents, there is a significant interest in the development of drug-eluting stents for other applications, such as the treatment of gastrointestinal (GI) cancers. Central to this process is understanding how particular drugs are released from stent coatings, which to a large extent is controlled by drug-polymer interactions. Therefore, in this study we investigated the release of docetaxel (DTX) from a selection of non-degradable polymer films. DTX-polymer films were prepared at various loadings (1, 5 and 10% w/w) using three commercially available polymers including poly(dimethylsiloxane) (PSi), poly (ethylene-co-vinyl acetate) (PEVA) and Chronosil polyurethane (PU). The formulations were characterised using different techniques such as photoacoustic Fourier-transform infrared (PA-FTIR) spectrophotometry, X-ray diffraction (XRD) and differential scanning calorimetry (DSC). The effect of DTX on the mechanical properties of the films, in-vitro release, and degradation tests were also assessed. For all polymers and DTX loadings, the drug was found to disperse homogenously without crystallisation within the polymer matrix. While no specific interactions were observed between DTX and PSi or PEVA, hydrogen-bonding appeared to be present between DTX and PU, which resulted in a concentration-dependent decrease in the Young’s moduli of the films due to disruption of inter-polymeric molecular interactions. In addition, the DTX-PU interactions were found to modulate drug release, providing near-linear release over 30 days, which was accompanied by a significant reduction in degradation products. The results indicate that DTX-loaded PU films are excellent candidates for drug-eluting stents for the treatment of oesophageal cancer.

Comparative removal of Suwannee River natural organic matter and perfluoroalkyl acids by anion exchange: Impact of polymer composition and mobile counterion

Anion exchange resin (AER) adsorption is an established technology for water treatment and groundwater remediation. Two contaminants amenable to AER treatment are natural organic matter (NOM) and per- and polyfluoroalkyl substances (PFAS), specifically anionic perfluoroalkyl acids (PFAAs) such as perfluorooctanoate (PFOA) and perfluorooctane sulfonate (PFOS). NOM is ubiquitous in natural waters and is often targeted for removal. PFAS occurrence in water resources is a human health concern. Accordingly, the goal of this research was to provide new insights on the use of AER for water treatment considering separate and combined removal of NOM and PFAAs. Batch experiments were conducted comparing polystyrene and polyacrylic AER in both chloride- and sulfate-forms using natural groundwater spiked with Suwannee River natural organic matter (SRNOM) and/or six PFAAs. The polymer composition of the AER had a significant impact on contaminant removal with polystyrene resin more effective for PFAA removal and polyacrylic resin more effective for SRNOM removal. Both resins had type I quaternary ammonium functional groups; however, the polyacrylic resin had trimethyl ammonium whereas the polystyrene resin had triethyl ammonium. Therefore, the influence of polymer composition could not be isolated conclusively from functional group chemistry. Polystyrene AER showed greater removal of PFAAs with sulfonate than carboxylate head group and 8-carbon than 4-carbon chain length. Removal of SRNOM and PFAAs by both resin polymer compositions were greater when sulfate was the mobile counterion ion than chloride. The results of this research have important implications for using AER for water treatment and remediation. Foremost, polymer composition and mobile counterion form of the resin can be selected to target specific contaminants and maximize contaminant removal. When contaminants have unique interactions with AER such as SRNOM and polyacrylic resin and PFAAs and polystyrene resin, the presence of one contaminant does not impact removal of the other contaminant.

The benzyl ethyl trithiocarbonate mediated control synthesis of a block copolymer containing N-vinyl pyrrolidone by RAFT methodology: Influence of polymer composition on cell cytotoxicity and cell viability

Benzyl ethyl trithiocarbonate (BET) mediated reversible addition–fragmentation chain transfer (RAFT) polymerization was carried out in dry 1,4-dioxane medium at 85 °C to synthesize Poly(n-Butyl Acrylate) (PBA) with pre-determined molecular weight (Mn 7999), narrow polydispersity (PDI 1.13) and precise chain end structure. The end chain functionality of macro chain transfer agent (CTA) was proved by homo-chain and hetero-chain extension polymerization experiment to get the poly (n-Butyl Acrylate) (Mn 17902) and poly (n-Butyl Acrylate)-b-poly(N-Vinyl Pyrrolidone) di-block copolymer (Mn 16029) respectively. Resulting polymers were characterized by 1H NMR, FTIR, GPC, TGA-DTA, DTG, DSC. The kinetic investigations confirmed the pseudo-first-order kinetic of the homopolymerization and linear evolution of the molar mass w.r.t. conversion within the range of polydispersity (PDI) (1.11 –1.20) in dry 1, 4-dioxane medium. The cyto-toxicities of PBA Macro CTA and PBA-b-PNVP polymers were evaluated on RAW264.7 mouse macrophage cells. The cellular viability was found to be 60.31% and 77.83% at 250 μM concentration, respectively for the two polymers. The viability was found more at high concentrations of polymers. The mechanism of cell death associated with these polymers was further evaluated in terms of apoptosis and necrosis on MCF-7 cell lines. Both the polymers induced apoptotic-like changes in MCF-7 cells.

Influence of Polymer Composition and Substrate on the Performance of Bioinspired Coatings with Antibacterial Activity

A series of methacrylic copolymers bearing thiazolium cationic groups and catechol moieties were evaluated as antibacterial coatings on a variety of materials including aluminum and plastics such as polycarbonate, poly(methyl methacrylate), and silicone rubber. The thermal properties of the copolymers were first studied by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The cationic copolymers were thermally stable up to 200 °C and presented glass transition temperatures values well above 100 °C; thus, an acceptable thermal behavior for typical biomedical applications. The cationic copolymers with variable content of the adhesive anchoring N-(3,4-dihydroxyphenethyl) methacrylamide (DOMA) units were coated onto the metal and polymeric substrates by drop casting and the adhesive properties of the obtained coatings were further evaluated as a function of DOMA content and substrate. Optical profilometry, attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectra, and antimicrobial studies reveal that the coatings adhere stronger to metal substrates than to the polymeric substrates. The copolymers with higher content of DOMA, 24 mol.%, resist solvent erosion treatment when coated onto all substrates and exhibit antimicrobial activity against Gram-positive S. aureus bacteria after this erosion treatment. In contrast, copolymers with low content, 9 mol.% of DOMA, only remain attached onto the aluminum metal substrate after solvent treatment, while on polymeric substrates the coatings are almost removed and do not show any efficacy against S. aureus bacteria.

Influence of polymer composition and drug loading procedure on dual drug release from PLGA:PEG electrospun fibers

Poly(lactide-co-glycolide) (PLGA) has been widely investigated for fabricating electrospun fibers due to their biocompatibility, paired with the capacity for encapsulating different drugs. However, such scaffolds shrink and distort upon contact with biological media, which is undesired for local drug application. To address this issue, we fabricated composite fiber scaffolds with the combination of PLGA and poly(ethylene glycol) (PEG). Scaffold shrinkage could successfully be overcome, however, the release kinetics of the encapsulated drug was strongly dependent on the amount of PEG. The addition of 5% PEG resulted in slower drug release due to a significant increase in fiber diameters. In contrast, the drug release rate was accelerated for fibers containing 10% PEG due to the water-soluble nature of the polymer. Furthermore, co-delivery of two different drugs, the small molecule acyclovir and the model protein bovine serum albumin was realized by two different approaches, coaxial electrospinning and immobilization of the drugs on the surface of the fibers, and drug release was found to be strongly dependent on the loading procedure. Based on our findings, key factors for understanding and controlling physicochemical properties of PLGA/PEG composite fibers as well as tuning drug release could be identified, providing an essential basis for rational design of electrospun fiber-based drug carriers.

Polypropylene-Based Porous Membranes: Influence of Polymer Composition, Extrusion Draw Ratio and Uniaxial Strain.

Several commercial grades of homo-polymer and its blends were selected to prepare microporous membranes through melt extrusion-annealing-uniaxial stretching technique (MEAUS). Branched or very fluid polypropylene was employed to modify the polymeric composition. In some blends, micro-sized calcium carbonate was added. We analysed the influence of sample composition, extrusion draw ratio, and we performed a deep study concerning the uniaxial strain rate, using in some cases extreme strain rates and strain extents. The crystalline features were studied by Differential Scanning Calorimetry (DSC), and the morphology of porous structure was analyzed through Scanning Electron Microscopy (SEM). Thermal stability and thermomechanical performance was measured by thermogravimetric analysis (TGA) and dynamic-mechanical-thermal (DTMA) study. A close relationship was found between crystalline characteristics, porous morphology and the trends registered for permeability.

Photocrosslinking of Polyglycidol and Its Derivative: Route to Thermoresponsive Hydrogels.

Hydrogels of biologically well-tolerated, high-molar-mass polyglycidol (PGl) and its thermoresponsive derivative poly(glycidol-co-ethyl glycidyl carbamate) have been obtained by direct UV crosslinking in the solid state. Polymers with molar masses up to 1.45 × 106 g mol-1 were crosslinked in the presence of benzophenone or (4-benzoylbenzyl)trimethylammonium chloride as photosensitizers. The photosensitizer concentration was varied from 2 to 10 wt%. The influence of polymer composition and photosensitizer type and amount on the crosslinking efficiency, swelling and temperature behavior of the obtained hydrogels was investigated. The photocrosslinking of PGl and poly(glycidol-co-ethyl glycidyl carbamate) led to hydrogels with swelling degrees up to 1700%. The swelling degrees of the hydrogels decreased with the increase of the environmental temperature indicating the thermoresponsive nature of gels. The swelling of obtained gels can be controlled by varying the composition of the copolymer precursor and by the network density.

Influence of polymer composition on the sensitivity towards nitrite and nitric oxide of colorimetric disposable test strips.

The influence of polymer composition on the sensitivity towards nitrite (NO2-) and nitric oxide (NO) of a series of 19 polymeric hydrogel films has been studied. The polymers, based on the hydrophilic monomer 2-hydroxyethylmethacrylate (HEMA), are able to encapsulate the colorimetric indicator 1,2-diaminoanthraquinone (DAQ) and to respond to NO2- and NO by visual changes. In the case of nitrite, the calculated limits of detection (LOD) for two of the polymeric sensors (10μM) are very close to the sensitivity estimated for free DAQ in solution (LOD 5μM), but with the advantage of a solid supported sensor with the format of a disposable test-strip made with affordable starting chemicals. The results are interpreted taking into account the nature and proportions of monomers and cross-linkers used for the synthesis of polymers. Key factors for obtaining sensitive materials are the hydrophilic character of the film along with the utilization of low levels of cross-linker and the use of an acidic monomer, like acrylic acid, as a building block.

Optimizing the sputter deposition process of polymers for the Storing Matter technique using PMMA.

Quantitative analyses in secondary ion mass spectrometry (SIMS) become possible only if ionization processes are controlled. The Storing Matter technique has been developed to circumvent this so-called matrix effect, primarily for inorganic samples, but has also been extended to organic samples. For the latter, it has been applied to polystyrene in order to investigate the extent of damage in the polymer, its fragmentation during the sputter deposition process and the effect of the deposition process on the spectra taken by Time-of-Flight SIMS (ToF-SIMS). In this work, a multi-technique approach, which employs the Storing Matter technique for deposition and ToF-SIMS and X-ray photoelectron spectroscopy for characterization, is used to enhance the control of the deposition process, including the thickness of the deposit, the alteration of the source film and the influence of polymer composition on the Storing Matter process. Poly (methyl methacrylate) (PMMA) is used for this work. More detailed information about the sticking of polymer fragments on the metal collector is obtained by density functional theory calculations. This work allows for the conclusion that a part of the fragments deposited on the collector surface diffuses on the latter, reacts and recombines to form larger fragments. The behaviour observed for PMMA is similar to polystyrene, showing that oxygen has no major influence on the processes occurring during the sputter deposition process. Additionally, we have developed a new methodology using 2D ToF-SIMS images of the deposit to monitor the deposit thickness and to identify surface contaminations. The latter are not only located at the position of the deposit but all over the collector surface. Copyright © 2016 John Wiley & Sons, Ltd.

Polymer-coated fluorescent CdSe-based quantum dots for application in immunoassay

The paper describes all stages of synthesis and characterization of biocompatible CdSe-based core/shell quantum dots (QDs) and their application as fluorescent label for immunoassay. Special attention was focused on development of maleic anhydride-based amphiphilic polymers for QDs solubilization in aqueous media. In this work two PEG-amines were tried for polymer modification: monoamine Jeffamine M1000 used previously in some researches and diamine Jeffamine ED-2003 applied for the first time for QDs solubilization. The use of different Jeffamines allows us to obtain QDs with carboxyl or amine functional groups available for conjugation. The influence of polymer composition on optical properties of the nanocrystals and their stability in aqueous solutions as well as on their conjugation with biomolecules was studied. QDs with different coatings were used as biolabels in quantitative fluorescence microtiter plate immunoassay and qualitative on-site column test. It was found that quantum dots covered with amphiphilic polymer prepared from poly(maleic anhydride-alt-1-octadecene) and Jeffamine ED-2003 retained up to 90% of their initial brightness, easily conjugated with protein and showed low non-specific adsorption. In optimized conditions the obtained QDs were successfully used for determination of mycotoxin deoxynivalenol in wheat and maize samples by fluorescence microtiter plate immunoassay with an IC50 of 220μgkg−1 and by on-site column test with cut-off of 500μgkg−1.

Biodegradable paclitaxel‐loaded microparticles prepared from novel block copolymers: influence of polymer composition on drug encapsulation and release

This study covers the preparation of microspheres for the controlled and targeted release of paclitaxel, using novel degradable polymers as carrier materials. Paclitaxel-loaded microspheres were prepared by oil-in-water single-emulsion solvent extraction/evaporation technique by using a series of polyurethanes and a block copolymer; the physicochemical properties of these polymers were modulated by changing nature and composition of their structural units. The obtained microparticles showed a regular morphology and properties (diameter: 1-100 µm; resuspension index: 18.8-100%; encapsulation efficiency: 26.6-97.2%) depending on polymer hydrophilicity and emulsifier used. In vitro release curves showed in all cases almost zero-order kinetics after an initial low burst effect (from 1 to 8.4%), which is required to minimize the drug side effects. This work also proposes a novel strategy to combine a controlled and a targeted release through the functionalization of the polymer matrix with peptide sequences. An RGD-functionalized polyurethane was used to successfully prepare paclitaxel-loaded microparticles. Studies on the preparation of polymer microspheres are reported.

Hollow fibers of poly(lactide-co-glycolide) and poly(ε-caprolactone) blends for vascular tissue engineering applications

At present the manufacture of small-diameter blood vessels is one of the main challenges in the field of vascular tissue engineering. Currently available vascular grafts rapidly fail due to development of intimal hyperplasia and thrombus formation. Poly(lactic-co-glycolic acid) (PLGA) hollow fiber (HF) membranes have previously been proposed for this application, but as we show in the present work, they have an inhibiting effect on cell proliferation and rather poor mechanical properties. To overcome this we prepared HF membranes via phase inversion using blends of PLGA with poly(ε-caprolactone) (PCL). The influence of polymer composition on the HF physicochemical properties (topography, water transport and mechanical properties) and cell attachment and proliferation were studied. Our results show that only the ratio PCL/PLGA of 85/15 (PCL/PLGA85/15) yielded a miscible blend after processing. A higher PLGA concentration in the blend led to immiscible PCL/PLGA phase-separated HFs with an inhomogeneous morphology and variation in the cell culture results. In fact, the PCL/PLGA85/15 blend, which had the most homogeneous morphology and suitable pore structure, showed better human adipose stem cell (hASC) attachment and proliferation compared with the homopolymers. This, combined with the good mechanical and transport properties, makes them potentially useful for the development of small-caliber vascular grafts.

Recycling Waste Polymers in EAF Steelmaking: Influence of Polymer Composition on Carbon/Slag Interactions

Interactions between blends of metallurgical coke and polymers with EAF slag (30.5% FeO) at 1550°C have been investigated using a sessile drop arrangement to determine the influence the polymer and its chemical composition on carbon/slag interactions. Two polymers, namely polyethylene terephthalate (PET) and polyurethane (PU), were used in this study. The CO emissions during carbon/slag interactions for PET/Coke and PU/Coke blends were lower as compared to corresponding emissions from metallurgical coke. An improvement in slag foaming, as determined by the dynamic changes in the volume of the slag droplet, was observed when PET/Coke and PU/Coke blends were used compared to the coke alone. Relatively greater number of gas bubbles was found to be entrapped in the slag droplet along with reduced iron droplets. Higher level of H2O formation was also seen in the case of PET/Coke and PU/Coke blends as a result of FeO reduction by H2. These results indicate that volatiles (H2 and CH4) released from the polymer/coke blends can influence the interactions between carbon and slag (in addition to reduction reactions by solid carbon). This study shows that a variety of waste polymers can be utilised as a carbon resource in EAF steelmaking processes.

Biocompatibility testing of ABA triblock copolymers consisting of poly( L-lactic-co-glycolic acid) A blocks attached to a central poly(ethylene oxide) B block under in vitro conditions using different L929 mouse fibroblasts cell culture models

The biocompatibility of ABA triblock copolymers consisting of poly( L-lactide-co-glycolide) A blocks attached to a central poly(ethylene oxide), (PEO), B block was investigated under in vitro conditions. The ABA triblock copolymer was compared to commercially available Poly( D, L-lactide-co-glycolide) (PLGA) and reference materials in different L929 cell culture models according to the procedure recommended by the International Standard Organization (ISO). Different preparation methods: namely extraction, indirect contact and direct contact with polymer samples were compared. The extraction method seems to be the most sensitive assay, allowing estimates of IC 50 values. ABA and PLGA polymers showed excellent compatibility with L929 fibroblasts with all preparation techniques used. The influence of polymer composition and molecular weight on degradation rate as well as in vitro biocompatibility was then investigated. Changes in pH and osmolarity as well as lactic acid content of the extracts were determined and compared to in vitro degradation data of polymer films in phosphate buffered saline at 37°C evaluating molecular weight (GPC) and massloss (gravimetry). An acceleration of the degradation rate of the ABA triblock copolymers with increasing PEO content was observed. The in vitro cytotoxicity studies demonstrated that the three ABA polymers were well tolerated by fibroblasts in cell culture. One ABA polymer batch ABA2 showed unusual in vitro cytotoxicity in L929 fibroblasts, possibly related to the molecular weight of the PEO used for this particular batch or residual glycolic acid. Cell culture models for biocompatibility testing of polymers according to ISO are useful as screening models in characterizing biodegradable polymers, but they cannot replace animal testing. The extraction method in combination with the MTT assay allows quantitative ranking of cytotoxic properties with high sensitivity.

Influence of polymer composition on the thermal characteristics of sulfonated EPDM ionomers

AbstractDetailed thermal characterization of sulfo‐EPDM ionomers was carried out. The endotherms observed via differential scanning calorimetry (DSC) and multiple inflections observed via thermal mechanical analysis (TMA) are speculated to be due to associated ionic species in the polymers. A large time dependence of the DSC endotherm was observed, suggesting substantial variations in the nature of the ionic species over this period. The influence of ionomer composition on thermal characteristics was probed with whole polymers and polymer fractions. In general, trends in the DSC and TMA data paralleled those expected on the basis of the anticipated effect of polymer sulfonation level, molecular weight, and counterion type on the strength of the physical crosslinking of these polymers. Both the DSC endotherms and the TMA inflection regions are rationalized in terms of a previously developed ionic‐bond exchange model.

Kinetics of crystal growth of calcium sulfate dihydrate. The influence of polymer composition, molecular weight, and solution pH

A seeded crystal growth technique has been used to study the influence of solution pH and temperature ranging from 25 to 50 °C on the performance of polymers of varying functional groups as calcium sulfate dihydrate (CaSO4•2H2O, gypsum) crystal growth inhibitors. Results indicate that at constant temperature and at a constant solution pH, crystallization in the presence of polyacrylic acids is preceded by an initial slow growth reaction, hereafter called induction period, following which crystal growth of gypsum proceeds with a rate close to that in pure supersaturated solution. Results suggest that at a constant pH, polyacrylic acid concentration, molecular weight, and temperature greatly affect the duration of induction period. Kinetic data collected as a function of solution pH in the range 2.5 to 9.0 suggest that solution pH has a marked effect on the induction period. The observed dependence of induction period on solution pH may be explained in terms of the degree of ionization of polyacrylic acid. Among the polymers of varying functional groups studied, i.e. carboxyl, sulfonate, acrylamide, dimethyldiallylammonium, etc., only those polymers having carboxyl group showed marked inhibitory activity for the growth of gypsum crystals.

Influence of polymer compositions on the effectiveness of machining glass

Influence of polymer compositions on the effectiveness of machining glass

Controlled Release of a Luteinizing Hormone-Releasing Hormone Analogue from Poly(d,l-lactide—co-glycolide) Microspheres

The performance in vivo of nafarelin acetate, a potent analogue of luteinizing hormone-releasing hormone, microencapsulated in poly(d,l-lactide-co-glycolide), was evaluated. The influence of polymer composition and molecular weight on the estrus-suppressing activity of the microspheres in female rats was determined. Compound release was shown to be effected by polymer erosion rather than by diffusion. A triphasic release of compound was observed, which was adjusted by altering the critical parameters of the polymer. A mechanism for the release of the compound was proposed. The primary release phase was compound loss by diffusion from the surface of the microspheres. The secondary phase of subeffective rates of release occurred concomitantly with polymer hydrolysis and a decrease in its molecular weight, although it remained insoluble. Dissolution of low-molecular weight fragments and erosion of the bulk of the polymer then initiated the tertiary phase of release of compound.

The influence of polymer composition on the wear of the metal surface during fretting of steel on polymer

The effects of the nature of the polymer on the amount of metal wear during fretting of steel on polymers in laboratory air have been studied under a range of loads (130–330 g), amplitudes (3–10 μm) and frequencies (30–60 Hz). A number of polymers can cause damage to the metal, which takes the form of adhesive transfer of α-Fe 2O 3 particles to the polymer surface. The amount of metal wear depends on the polymer counterface and, under a given set of experimental conditions, increases in the order polytetrafluoroethylene (PTFE) and polyethylene, polyvinylidene fluoride (PVDF), polychlorotrifluoroethylene (PCTFE), polysulphone, Polyvinylchloride (PVC), polymethylmethacrylate (PMMA), polycarbonate, nylon 66. No metal wear occurs when the counterface is PTFE and only occurs with polyethylene when the amplitude is greater than 7 μm. These differences are explained in terms of the adhesive properties of the polymers, as determined by their surface energetics. Wear of the polymer during fretting takes the form of fibre formation for polysulphone, PVC, polycarbonate, nylon 66 and, to a small extent, polyethylene, while it takes the form of a transfer of a polymer film to the metal for PTFE and PVDF. No polymer wear occurs for PCTFE or PMMA.