Explore the vast range of titles available.

The water-soluble polymer PAM (polyacrylamide) is used in enhanced oil recovery (EOR) operations. It is pumped into water injection wells to increase the viscosity of the injected water and in turn to direct more oil towards production wells. This EOR process is proven to be sensitive to operational well conditions such as hydrocarbon reservoir temperature, as well as the salinity of the injected water and/or formation water. These operational conditions lead to technical challenges ranging from the solubility of PAM in injection water to the behaviour of PAM inside the reservoir. To gain a clear picture of the functionality of PAM in EOR applications, this report characterizes its behaviour of in terms of degree of hydrolysis and changes in solution viscosity determined using Perkin Elmer spectrum 100 Fourier transform infrared-Attenuated total reflection (FTIR)-ATR and nuclear magnetic resonance spectroscopy (1H NMR) and a Fann model 35 Couette and Cole Parmer rotational viscometer, respectively. Different shear rates were investigated to determine the effect of shear on PAM gel stability. Experiments were performed for PAM mixed with formation brine at 50, 70, and 90 °C for ageing times of up to 30 days. The results indicate that the degree of hydrolysis achieved after 30 days is much higher in saline solutions than in pure water, and that this effect is more pronounced at higher temperatures. For example, after 30 days at 50 °C, the hydrolysis level was observed to be 53%, rising to 65% at 70 °C and 75% at 90 °C in PAM mixed with brines. Similar trends were observed with viscosity, where lower viscosity was observed for samples at higher temperatures and salinities. It is thus reasonable to conclude that the degree of hydrolysis causes changes in the viscosity of the polymer gel, leading to a decline in its performance as it ages.

Triboelectricity PDMS‐based triboelectric nanogenerator (TENG) under nanoscale investigation, employing a scanning near‐field optical microscope. A conductive probe mounted at the end of the cantilever generates nanofocus for incident infrared irradiation, scattered light reveals the surface chemical properties of the pristine versus aged PDMS films. Breakage of SiO bonds results in the chain scission process that will degrade TENG performance. More details can be found in article 2400094 by Jin‐Chong Tan and co‐workers.

Atomic force microscopy (AFM) has been extensively used for the nanoscale characterization of polymeric materials. The coupling of AFM with infrared spectroscope (AFM-IR) provides another advantage to the chemical analyses and thus helps to shed light upon the study of polymers. This paper reviews some recent progress in the application of AFM and AFM-IR in polymer science. We describe the principle of AFM-IR and the recent improvements to enhance its resolution. We also discuss the latest progress in the use of AFM-IR as a super-resolution correlated scanned-probe infrared spectroscopy for the chemical characterization of polymer materials dealing with polymer composites, polymer blends, multilayers, and biopolymers. To highlight the advantages of AFM-IR, we report several results in studying the crystallization of both miscible and immiscible blends as well as polymer aging. Finally, we demonstrate how this novel technique can be used to determine phase separation, spherulitic structure, and crystallization mechanisms at nanoscales, which has never been achieved before. The review also discusses future trends in the use of AFM-IR in polymer materials, especially in polymer thin film investigation.

Aging has a serious impact on the properties of functional polymers. Therefore, it is necessary to study the aging mechanism to prolong the service and storage life of polymer-based devices and materials. Due to the limitations of traditional experimental methods, more and more studies have adopted molecular simulations to analyze the intrinsic mechanisms of aging. In this paper, recent advances in molecular simulations of the aging of polymers and their composites are reviewed. The characteristics and applications of commonly used simulation methods in the study of the aging mechanisms (traditional molecular dynamics simulation, quantum mechanics, and reactive molecular dynamics simulation) are outlined. The current simulation research progress of physical aging, aging under mechanical stress, thermal aging, hydrothermal aging, thermo-oxidative aging, electric aging, aging under high-energy particle impact, and radiation aging is introduced in detail. Finally, the current research status of the aging simulations of polymers and their composites is summarized, and the future development trend has been prospected.

This review is conceived as a guide for material science researchers and conservators aiming to face the problem of deterioration of contemporary artworks entirely or partially made of plastics. It initially illustrates the analytical approaches for identifying polymeric material components in 3D art objects, such as sculptures and installations, and provides a perspective of their limits and advantages. Subsequently, the methodologies used for studying the deterioration of contemporary art plastics are reviewed, emphasising the main effects of the different types of degradation (i.e., migration of additives, oxidation and hydrolysis) and suggesting the appropriate techniques for their detection. Finally, the application of artificial ageing tests is critically assessed. All the concepts are elaborated through case studies and examples.

Essential oils have been identified as effective natural compounds to prevent bacterial infections and thus are widely proposed as bioactive agents for biomedical applications. Across the literature, various essential oils have been incorporated into electrospun fibres to produce materials with, among others, antibacterial, anti-inflammatory and antioxidant activity. However, limited research has been conducted so far on the effect of these chemical products on the physical characteristics of the resulting composite fibres for extended periods of time. Within this work, electrospun fibres of poly(lactic acid) (PLA) were loaded with the essential oil limonene, and the impact of storage conditions and duration (up to 12 weeks) on the thermal degradation, glass transition temperature and mechanical response of the fibrous mats were investigated. It was found that the concentration of the encapsulated limonene changed over time and thus the properties of the PLA–limonene fibres evolved, particularly in the first two weeks of storage (independently from storage conditions). The amount of limonene retained within the fibres, even 4 weeks after fibre generation, was effective to successfully inhibit the growth of model microorganisms Escherichia coli, Staphylococcus aureus and Bacillus subtilis. The results of this work demonstrate the importance of evaluating physical properties during the ageing of electrospun fibres encapsulating essential oils, in order to predict performance modification when the composite fibres are used as constituents of medical devices.

Ageing of elastomeric materials in triboelectric nanogenerators (TENGs) often leads to compromised electrical performance and can greatly affect their real‐world application as next‐generation energy harvesters and self‐powered sensors. Herein, the ageing behavior of PDMS‐based TENGs is investigated by probing the dielectric and mechanical properties of the membrane materials. Over time, ageing of PDMS after 17 months is evinced by a decline by 71%, 68% and 52% in open‐circuit voltage, short‐circuit current and charge transfer, respectively, and an increase by 6.8 times in surface charge decay rate. The reduced electrical performance can be attributed to a decrease in work function, dielectric constant, surface adhesion and heterogeneity in stiffness, as well as an increase in loss tangent. The effect of chemical chain scission on the PDMS surface is confirmed through nearfield infrared nanospectroscopy. This study gives insights into the underlying mechanism behind the ageing of PDMS‐based TENGs, paving the way to future work for ameliorating these ageing‐related issues with the aim to ensure long‐term stability of practical triboelectric devices. The effect of ageing on the electrical charge harvesting capacity of polydimethylsiloxane (PDMS)‐based triboelectric nanogenerators is interrogated through dielectric and mechanical characterization at micro‐ and nanoscale resolutions. Nanospectroscopic study reveals the physicochemical mechanism underpinning the evolution of interfacial properties that influence the long‐term stability of triboelectric elastomers.

This work investigated the sorption and the diffusion properties of CO2 under high pressure and the further modificationsinduced in Poly(lactic acid) (PLA) thin layers. Poly(ethylene terephtalate) (PET) was also considered for comparativepurposes. Firstly, from thermodynamic equilibrium, the CO2 sorption isotherm (two sorption-desorption cycles, up to25 bar, at 25 °C) gave strong evidence of a physisorption mechanism and of a hysteresis phenomenon. Infrared spectroscopyanalysis confirmed that no chemical reaction occurred. Secondly, from the kinetics aspect, the CO2 diffusion coefficient wasfound around 10–13 m2·s–1 and was slightly faster for sorption compared to desorption. Additionally, when CO2 sorption occurred,the PLA structure and its functional properties were modified due to plasticization and swelling. CO2 plasticizationreduced the glass transition temperature of PLA and accelerated the physical ageing of the polymer. These results are thereforeof significant importance in industrial processing and applications which involve close contact between CO2 and PLA.

Cables, especially their insulation and jacket materials made of polymers, are vulnerable to ageing degradation during normal operation. However, they must remain functional for the entire life of a nuclear power plant, or even in the event of an accident for cables with a safety requirement. This study focuses on models of crosslinked polyethylene (XLPE)-based insulation of cables and deals with the structure modification and the behavior of XLPE for nuclear applications due to the effect of additives. Various additives are added to the polymer formulation to evaluate their impact on ageing. The samples are irradiated at room temperature by several gamma doses, up to 374 kGy, with two dose rates (40 Gy/h and 300 Gy/h) and compared with a non-irradiated sample used as reference. To understand the impact of gamma irradiation on the materials, the principal component analysis (PCA) method is applied on spectra recorded through attenuated total reflectance–Fourier transform infrared (ATR-FTIR) spectroscopy. The results highlight the effects of ageing depending on the dose rate and on the formulation of the materials, with the identification of different degradation products. A curve resolution study compares the effects of different additives on polymer oxidation and shows that the low dose rate leads to a higher degradation than the high dose rate.

The clutch facing is a complex organic matrix composite in dry clutch systems. When the clutch engages, there is a sliding contact between the clutch facing and the mating surfaces, resulting in temperature increases of up to 300 °C. These thermal cycles activate several mechanisms that can have consequences on such material: cracking and, more generally, the ageing of the polymer. The thermomechanical properties of the material therefore evolve according to the number of thermal cycles. This study focused on investigating the local and average evolution of the coefficients of thermal expansion (CTE) of clutch facing as a function of thermal cycles. Several techniques were employed, including image stereocorrelation for determining the CTE, Dynamic Mechanical Analysis (DMA) tests for monitoring the ageing of the material and acoustic emission for highlighting the damage. The results showed that the average CTE decreased as a function of the temperature and the number of loading cycles, while locally, it increased in some areas and decreased in others. These differences appear to be the result of material heterogeneity (actual yarn tracing, etc.) and interaction between cracking and ageing mechanisms in the polymer matrix. Indeed, thermal cycling led to cracking and additional crosslinking, which is influenced by ageing conditions.