Modification Of Polyethylene Research Articles

Extrusion and Injection Molding of Polyethylene Loaded with Recycled Textiles: Mechanical Performance and Thermal Conductivity

The aim of this project was to assess the thermal conductivity of polyethylene (PE) filled with carbon black (CB), specifically for geothermal pipes. The project explored the potential modification of PE’s thermal conductivity by incorporating recycled textile fibers. Different types of shredded recycled fibers were tested, including two types of polyamide fibers with varying contaminations and one type of polyester fiber. Following several preparation steps, various composite materials were manufactured and compared to bulk PE using various testing methods: Differential Scanning Calorimetry analysis (DSC), mechanical testing (flexural and tensile), and laser flash analysis (LFA). The results revealed alterations in the mechanical properties of the composite materials in comparison to PE filled with CB. The LFA tests demonstrated the effectiveness in reducing polymer thermal diffusivity at higher temperatures, particularly when the material was loaded with recycled polyester fillers.

Thermomechanical Properties of Ramie Fiber/Degradable Epoxy Resin Composites and Their Performance on Cylinder Inner Lining.

Type IV gas cylinders are widely used in the field of vehicles due to their advantages such as light weight, cleanliness, and low cost. Ramie fiber/degradable epoxy resin composites (RFRDE) provide new ideas for the material selection of Type IV gas cylinders due to their advantages of low carbon emissions, low environmental pollution, and renewable resource utilization. However, the poor interfacial bonding strength and moisture resistance between polyethylene plastics and RFRDE have limited their application areas. This study tested the mechanical properties of ramie fibers at different heat treatment temperatures, and studied the thermal mechanical properties of RFRDE through differential scanning calorimeter and curing kinetics methods. At 180 °C, the tensile strength of fiber bundles decreased by 34% compared to untreated fibers. As the highest curing temperature decreases, the tensile strength of RFRDE increases but the curing degree decreases. At the highest curing temperature of 100 °C, the tensile strength of RFRDE is 296 MPa. The effect of the corona discharge and flexible adhesive on the surface modification of polyethylene was analyzed using scanning electron microscopy. These results provide guidance for the development of natural fiber/degradable epoxy resin composite materials.

Proposing an Affordable Plasma Device for Polymer Surface Modification and Microbial Inactivation.

This study proposes an affordable plasma device that utilizes a parallel-plate dielectric barrier discharge geometry with a metallic mesh electrode, featuring a straightforward 3D-printed design. Powered by a high-voltage supply adapted from a cosmetic plasma device, it operates on atmospheric air, eliminating the need for gas flux. Surface modification of polyethylene treated with this device was characterized and showed that the elemental composition after 15 min of plasma treatment decreased the amount of C to ~80 at% due to the insertion of O (~15 at%). Tested against Candida albicans and Staphylococcus aureus, the device achieved a reduction of over 99% in microbial load with exposure times ranging from 1 to 10 min. Simultaneously, the Vero cell viability remained consistently high, namely between 91% and 96% across exposure times. These results highlight this device's potential for the surface modification of materials and various infection-related applications, boasting affordability and facilitating effective antimicrobial interventions.

Modification of polyethylene for oil-water separation in industrial wastewater treatment

Low-density polyethylene (LDPE) is extensively used worldwide in various applications due to its versatile features and abundant commercial availability. This study investigated, for the first time, the beneficial use of a novel chemically modified commercial-grade LDPE as a sorbent for oil-water separation in industrial wastewater treatment. Several laboratory tests were conducted in batch and continuous fixed-bed modes to evaluate the LDPE adsorbent’s capacity, performance repeatability and recyclability under relevant field conditions. These results were compared to walnut shell (WS), a widely used sorbent for removing oil from industrial wastewaters, including produced water from oil and gas operations. Untreated LDPE achieved higher total organic carbon (TOC) removals and retention capacities, ∼20 % and ∼66 mg/g, respectively, when compared to untreated WS, <5 % and <1 mg/g, respectively. Improved kinetics and adsorption behavior favorability were achieved for LDPE after chemical modification using a cationic monomer. Both the chemically treated LDPE and WS showed comparable TOC removal rates (ranging from 60 % to 80 %). However, the modified LDPE exhibited higher sorption capacities (∼61 mg/g) compared to the treated WS (8.0 mg/g). Chemical regeneration of LDPE with toluene demonstrated superior performance recovery (>90 %) when compared to physical cleaning with deionized water (<40 %). The study presented promising results in advancing novel materials like LDPE to support circular economy in industrial wastewater treatment.

Modification of High-Density Polyethylene with a Fibrillar-Porous Structure by Biocompatible Polyvinyl Alcohol via Environmental Crazing.

Polymer/polymer nanocomposites based on high-density polyethylene (HDPE) and biocompatible polyvinyl alcohol (PVA) were prepared by tensile drawing of HDPE in the PVA solutions via environmental crazing. The mechanism of this phenomenon was described. The HDPE/PVA nanocomposites were studied by the methods of scanning electron microscopy, atomic force microscopy, gravimetry, tensile tests, and their composition, properties, and performance were characterized. The content of PVA in the HDPE/PVA nanocomposites (up to 22 wt.%) was controlled by the tensile strain of HDPE and concentration of PVA in the solution. Depending on the content of PVA, the wettability of the HDPE/PVA nanocomposite (hydrophilic-lipophilic balance) could be varied in a broad interval from 45 to 98°. The modification of HDPE by the biocompatible PVA offers a beneficial avenue for practical applications of the HDPE/PVA composites as biomedical materials, packaging and protective materials, modern textile articles, breathable materials, membranes and sorbents, etc.

Surface modification of polyethylene using argon and argon/methane DBD atmospheric pressure plasma jet

This article investigates the surface modification of polyethylene (PE) using an atmospheric pressure plasma jet of the DBD type (APPJ) maintained with pure argon (Ar) and with a premixed gas containing 90% argon and 10% of CH4. First and for both plasma jets, the jet length and the optical emissions coming from the plasma species were studied in terms of flow rate and applied voltage. Comparing to Ar, it has been shown that when the premixed gas is used, the jet length gets smaller, the transition point from laminar to turbulent regime was shifted to a low flow rate, and the emission of CH, H2 and C2 appeared, while O and N2 emission coming from ambient air was quenching. The PE surface treatment in both laminar and turbulent regime has been evaluated using water contact angle (WCA) measurement and attenuated total reflection (ATR). The obtained results showed that the hydrophilicity of PE has been improved in both plasma jets due to oxygen group (C=O) incorporation, but Ar plasma jet was observed to induce surface degradation compared to Ar/CH4 plasma due to the higher excited species.

Facile physical modification of ultrathin polyethylene by trace poly(vinyl alcohol)

Poly (vinyl alcohol) (PVA) modification to nonpolar polymers has been intensively investigated due to the performance improvement in membrane separation, tissue engineering, and other applications. Slightly deviated from the conventional route, no covalent bonding by crosslinking or hydrogen bonding is needed to anchor PVA onto the target matrix. This work harnessed van der Waals interaction only to achieve the modification. Owing to the high surface energy and aspect ratio of ultra-high molecular weight polyethylene (UHMWPE) ultrathin membranes, the physical binding between PVA and PE was found stable and easy to establish. This interaction is initiated by the entropy-driven hydrophobic effect at the liquid-solid interface to reduce surface energy. By encapsulation of PVA on the fibrils, the PE hydrophilicity could be overturned (from 134.6° to 48.4°) with micro-structures remaining almost intact at the low loading of modification (0.001% conc. solution dip-coating). The resultant hydrophilic ultrathin PVA-PE membranes showed high transparency, high mechanical strength (380 MPa in tensile max. stress), and high porosity with only 200 nm thickness in a freestanding state. This work provides a facile approach to switch the hydrophilicity of nonpolar polymer ultrathin membranes by establishing vdW physical bonding only. By trace-adsorption, this method could also be helpful in fine-tuning nanostructures of the target polymer matrix by a resolution of nanometer level.

Modification of High-Pressure Polyethylene and Ethylene–Vinyl Acetate Copolymer with Sepiolite Chain-Layered Silicate

Modification of High-Pressure Polyethylene and Ethylene–Vinyl Acetate Copolymer with Sepiolite Chain-Layered Silicate

PROPERTIES OF THE COMPOSITION BASED ON MODIFIED POLYETHYLENES

The subject of this paper is to study the properties of compositions based on a modified polyethylene and a thermoplastic polyolefin structural features. As a result of the modification of polyethylene, the high elasticity of the material grows, which outwardly makes this polymer similar in complex to the physico-mechanical properties of rubber. The calculations made allowed us to estimate the parameters of the observed thermal transitions and to assign them to the mobility of specific elem ents of the structure

Functionalization and Surface Modification of Mesoporous Hydrophobic Membranes by Oligomers and Target Additives via Environmental Crazing

This work offers an ecologically friendly and facile approach for the modification of high-tonnage commercial polymers, including polypropylene (PP), high-density polyethylene (HDPE), and poly(ethylene terephthalate) (PET), and preparation of nanocomposite polymeric membranes via incorporation of modifying oligomer hydrophilic additives, such as poly(ethylene glycol) (PEG), poly(propylene glycol) (PPG), polyvinyl alcohol (PVA), and salicylic acid (SA). Structural modification is accomplished via the deformation of polymers in PEG, PPG, and water-ethanol solutions of PVA and SA when mesoporous membranes are loaded with oligomers and target additives. The content of target additives in nanocomposite membranes is controlled by tensile strain, and the level of loading can achieve 35-62 wt.% for PEG and PPG; the content of PVA and SA is controlled by their concentration in the feed solution. This approach allows for the simultaneous incorporation of several additives which are shown to preserve their functional performance in the polymeric membranes and their functionalization. The porosity, morphology, and mechanical characteristics of the prepared membranes were studied. The proposed approach allows an efficient and facile strategy for the surface modification of hydrophobic mesoporous membranes: depending on the nature and content of target additives, their water contact angle can be reduced to 30-65°. Water vapor permeability, gas selectivity, antibacterial, and functional properties of the nanocomposite polymeric membranes were described.

Biostable Fluorine-Containing Coatings on the Surface of Polymers

We considered the formation of the integrated biostable coating on the surface of several polymers using the original gas-phase fluorination technology. The effectiveness of surface modification of low-density polyethylene (LDPE) and polypropylene (PP) was confirmed by corresponding changes in the absorption spectra of infrared radiation with the modified samples. The gas-phase fluorination quality of ultrahigh molecular weight polyethylene (UHMWPE) and nitrile butadiene rubber (NBR) surfaces was evidenced by the results of scanning electron microscopy (SEM) and energy dispersion analysis (EDS). As was shown with the direct measurements of water and ethyleneglycol wetting angles, the properties differences of the polymer materials with modified surfaces from the initial one correlated well with the change in free surface energy induced by the chemical and morphological transformations under the fluorine and oxygen-containing gas mixtures treatment. The developed technique for the bio-contamination degree quantifying, based on the computer analysis of the corresponding images, allowed us to establish that gas-phase fluorination of the surface approximately doubles the time during which the biofouling of LDPE, PP and UHMWPE with the mixed colony of Rivularia and Stigonema Minutum algae occurs under natural conditions. No positive effect from fluorination was observed for NBR, which was explained, from our point of view, by the difference in the mechanisms of biostability for the considered polymer materials.

Zwitterionic surface modification of polyethylene via atmospheric plasma-induced polymerization of (vinylbenzyl-)sulfobetaine and evaluation of antifouling properties

Zwitterionic polymer brushes were grafted from bulk polyethylene (PE) by air plasma activation of the PE surface followed by radical polymerization of the zwitterionic styrene derivative (vinylbenzyl)sulfobetaine (VBSB). Successful formation of dense poly-(VBSB)-brush layers was confirmed by goniometry, IR spectroscopy, XPS and ToF-SIMS analysis. The resulting zwitterionic layers are about 50–100 nm thick and cause extremely low contact angles of 10° (water) on the material. Correspondingly we determined a high density of > 1.0 × 1016 solvent accessible zwitterions/cm2 (corresponding to 2,0 *10-8 mol/cm2) by a UV-based ion-exchange assay with crystal violet. The elemental composition as determined by XPS and characteristic absorption bands in the IR spectra confirmed the presence of zwitterionic sulfobetaine polymer brushes. The antifouling properties of the resulting materials were evaluated in a bacterial adhesion test against gram-positive bacteria (S. aureus). We observed significantly reduced cellular adhesion of the zwitterionic material compared to pristine PE. These microbiological tests were complemented by tests in natural seawater. During a test period of 21 days, confocal microscopy revealed excellent antifouling properties and confirmed the operating antifouling mechanism. The procedure reported herein allows the efficient surface modification of bulk PE with zwitterionic sulfobetaine polymer brushes via a scalable approach. The resulting modified PE retains important properties of the bulk material and has excellent and durable antifouling properties.

Verification of mechanism for effect of silane coupling agent modification of polyethylene (PE) fiber's surface on strain-hardening behavior of high-strength cementitious composites

To fully understand the mechanism for the effect of silane coupling agent (SCA) modified polyethylene (PE) fiber on the strain-hardening behavior of high-strength cementitious composites (HSCC), an experimental research has been conducted, including direct tension and microstructural tests using optical microscope, scanning electron microscope (SEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The results showed that, compare to the interfacial bonding between original PE fiber and very high strength matrix of cementitious composite at water/binder ratio (W/B) of 0.18, the interfacial bonding was strengthened after the modification of PE fiber's surface by SCA solution of 3% concentration, which subsequently resulted in the improvement of initial-cracking stress, ultimate tensile stress and ultimate tensile strain from 5.20 MPa, 6.34 MPa and 0.68% to 7.26 MPa, 8.01 MPa and 5.06%, respectively. The mechanism for the improvement in strain-hardening behavior of HSCC with SCA-modified PE fiber was that the physicochemical interactions occurred between the SCA-modified PE fiber and the matrix. Among these interactions, amino and hydroxyl groups connected to the PE fiber improved the hydrophilicity of fiber surface, which enhanced the physical bonding between the SCA-modified PE fiber and the matrix. More importantly, two types of chemical interactions have been proved to establish chemical bonding between the PE fiber and matrix, namely, the condensation reaction between hydroxyl groups of the modification layer on the PE fiber and hydroxyl groups of C–S–H gels in the matrix, and the combination of the polymer of SCA's hydrolysates with Ca(OH)2 released by cement hydration.

Influence of various modifiers on the properties of recycled polyethylene, approaches to plastic recycling

The article presents the results of the research carried out by the specialists of POLYPLASTIC Group LLC on the modification of recycled polyethylene with small amount of various chemical additives. The results of the evaluation of the viscosity, physical and mechanical properties of the obtained materials, as well as rheological curves, are presented. Data on the introduction of antioxidants into recycled materials to improve thermal stability after recycling are presented. The use of this modifiers makes it possible to increase or decrease the viscosity of the material, while the strength properties are practically unchanged. The possibility of cross-linked polyethylene recycling is shown, data on the viscosity and physical and mechanical properties of the obtained granulate are given, which are close to the properties of extrusion grades.

Modification of high-density polyethylene and ethylene-vinyl acetate copolymer by chain-layered silicate «sepiolite»

Composites based on high-pressure polyethylene and ethylene-vinyl acetate copolymer, containing sepiolite clay powder with a chain-layered structure have been investigated, and their physical-mechanical properties have been analyzed. When using sepiolite, the organomodification and compatibilization are not required. It is shown, that composite materials with the addition of sepiolite are superior in a number of characteristics to those containing traditionally applied layered clay powders.

Ti and TiO2 magnetron sputtering in roll-to-roll fabrication of hybrid membranes

The large-scale surface modification of polyethylene terephthalate track-etched membranes (TM) using industrial roll-to-roll planar magnetron sputtering of Ti and TiO2 for use in advanced technologies such as separation, biotechnology, and microelectronics was investigated. The Ti and TiO2-Ti coated TM surface characterisation was done using a combination of scanning electron microscopy, atomic force microscopy, contact angle- and scratch adhesion testing. Structural characterisation was done using transmission electron microscopy, energy dispersive x-ray spectroscopy, x-ray photoelectron spectroscopy, and tensile testing. Water permeability and bubble point testing were used to confirm the membrane permeability after surface modification. A tensile test showed that the coated membranes’ strength was within an acceptable range of one another. Magnetron sputtering did not lead to significant changes in the water permeability, nor a notable reduction in the pore diameter of the resulting Ti-TM and TiO2-Ti-TM hybrid membranes. Sputtered coatings on top of the TM surface significantly reduced the water contact angle from 72° for an untreated TM to 33° and 28° for Ti-TM and TiO2-Ti-TM, respectively. This investigation shows that roll-to-roll magnetron sputtering is a viable approach to the large-scale fabrication of hybrid membranes based on TM as model support.

Generation and Characterization of Cold Atmospheric Pressure Plasma Jet for Surface Modification of High-Density Polyethylene

Cold atmospheric pressure plasma technology has a variety of applications in different fields including material science and biomedical science. It has been using for surface modification and material processing in material science and used to improve the wettability, adhesion and biocompability of polymeric surfaces without altering the entire bulk properties. This paper outlines the characterization of cold atmospheric pressure plasma jet, which was generated in a high frequency (20 kHz) and high voltage (3.5 kV) power supply, as well as its application in the surface modification of high density polyethylene. Electrical and optical characteristics are used to estimate the electron density of the plasma. The effect of plasma on the surface properties of the material are analyzed by calculating contact angle, surface energy measurements and analyzing scanning electron microscopy images. Adhesive bonding strength and numerous other attributes have increased, however surface treatment is the process of cleaning, etching, functionalizing, and chemically treating substrates to improve roughness and adhesive properties on the surface. Cold plasma can induce a soft roughening on the surface through ion bombardment with polar functional groups resulting in the decrease in water contact angle.

Comparison of surficial modification of micro-sized polyethylene in between by UV/O3 and UVO submerged system

This study examined the effects of ozonation and UV applied in series (O3+UV) or simultaneously (UVO) under four different ozone dosages from 4 to 7 mg/min to understand the surface alterations on polyethylene microplastics in aquatic environments via the photochemical oxidation process. The plastic samples were analyzed by Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and contact angle measurements. FTIR spectroscopy showed that the levels of carbonyl (ketone and esters) and vinyl groups increased gradually with increasing ozone dose injected; the highest was observed at 6 mg/min of ozone. On the other hand, the levels at 7 mg/min of ozone were slightly lower than those at 4 to 6 mg/min. This could be related to the deeper penetration into the crystalline bulk polymeric chain. The contact angle changed from 125.90˚ to the lowest value of 120.04˚ and 123.8˚ for O3+UV and UVO, respectively. Furthermore, XPS showed that C-O was only presented in the 7 mg/min sample, whereas C-O, OH, C=O, and C-C=O remained for 4 to 6 mg/min. Overall, O3+UV can oxidize the surface of the polyethylene microplastic particles more effectively than those of UVO, irrespective of the ozone dosages.

Modification of polyethylene terephthalate track etched membranes by planar magnetron sputtered Ti/TiO2 thin films

This study investigates the surface modification of polyethylene terephthalate track-etched membranes by planar magnetron sputtering of titanium and titanium dioxide thin films to improve its hydrophilicity and photocatalytic activity. After cold plasma treatment to enhanced adhesion, Ti thin films were deposited by planar magnetron sputtering and TiO2 thin films by reactive magnetron sputtering in an Ar-O2 gas atmosphere. The morphology of the deposited thin films was characterised using atomic force microscopy and scanning electron microscopy. The pores retained a mostly circular shape. However, the modified track membrane's surface pore diameter reduced from 0.2 µm to 0.15 µm for Ti coated samples and 0.08 µm for Ti-TiO2 coated samples. Structural studies using X-ray photoelectron spectroscopy, energy-dispersive X-ray spectroscopy and Raman spectroscopy of Ti and TiO2 thin films revealed the intricate composition of the sputtered thin films which was a result of the complexity of sputtering on top of the porous polymer support. Additional investigations in surface wettability and bandgap showed a significant change in the track membrane surface's hydrophilicity and photocatalytic properties after depositing TiO2-Ti, adding to the self-cleaning properties of the coated TM. The bandgap of the film was 3.1 eV and of the indirect type. Both Ti and TiO2-Ti sputtering over the TM surface significantly reduced the water contact angle from 72° for untreated PET to 43° and 45° for Ti-TM and TiO2-Ti-TM, respectively. This study shows that planar magnetron sputtering is a viable approach to surface modification of a porous polymeric support, such as track-etched membranes. The sputtered coating enhanced membrane hydrophilicity, thereby reducing the chance of surface fouling by organic substances, which leads to improved self-cleaning properties.

Influence of ionic liquids on mechanical and thermal properties of polyethylene from renewable resources

Polyethylene from renewable resources produced using sugarcane as raw material was modified with phosphonium ionic liquids. Tensile properties and thermal behavior of modified biopolyethylene in air and nitrogen atmosphere were studied. The thermal degradation of ionic liquids and their influence on thermal degradation of polyethylene from renewable resources were studied by thermogravimetric analysis (TGA). In general, modification of biopolyethylene with phosphonium ionic liquids resulted in improvement of tensile properties, i.e., tensile strength and Young’s modulus. Thermal degradation of biopolyethylene modified with phosphonium ILs proceeds in one step in the range of 400–500 °C in nitrogen atmosphere. Modification of polyethylene with trihexyltetradecylphosphonium bis(2,4,4-trimethylpentyl)phosphinate ionic liquid resulted in increase in DTGpeaks and T10% temperatures toward higher temperature for modified polyethylene in comparison with unfilled PE sample both in air and nitrogen atmosphere.