Polymer Technology Research Articles

Biodegradable Polymer Versus Polymer-Free Ultrathin Sirolimus-Eluting Stents: Analysis of the Stent Arm Registry From the HOST-IDEA Randomized Trial.

The efficacy and safety of each third-generation drug-eluting stent with ultrathin struts and advanced polymer technology remain unclear. We investigated the clinical outcomes of percutaneous coronary intervention using the Coroflex ISAR polymer-free sirolimus-eluting stent (SES) or Orsiro biodegradable polymer SES. The HOST-IDEA trial (Harmonizing Optimal Strategy for Treatment of Coronary Artery Stenosis-Coronary Intervention With Next-Generation Drug-Eluting Stent Platforms and Abbreviated Dual Antiplatelet Therapy), initially designed with a 2×2 factorial approach, sought to randomize patients undergoing percutaneous coronary intervention based on dual antiplatelet therapy duration (3 versus 12 months) and stent type (Coroflex ISAR versus Orsiro). Despite randomizing 2013 patients for dual antiplatelet therapy duration, the stent arm transitioned to a registry format during the trial. Among these, 328 individuals (16.3%) were randomized for Coroflex ISAR or Orsiro SES, while 1685 (83.7%) underwent percutaneous coronary intervention without stent-type randomization. In this study, the Coroflex ISAR (n=559) and Orsiro groups (n=1449) were matched using a propensity score. The prespecified primary end point was target lesion failure, a composite of cardiac death, target vessel myocardial infarction, and clinically driven target lesion revascularization at 12 months. The baseline patient and procedural characteristics were well balanced between the Coroflex ISAR and Orsiro groups after propensity score matching (n=559, each group). The Coroflex ISAR group was significantly associated with a higher rate of target lesion failure, mainly driven by clinically driven target lesion revascularization, compared with the Orsiro group (3.4% versus 1.1%; hazard ratio, 3.21 [95% CI, 1.28-8.05]; P=0.01). A higher risk of target lesion failure in the Coroflex ISAR group was consistently observed across various subgroups. The rates of any bleeding (hazard ratio, 0.85 [95% CI, 0.51-1.40]; P=0.52) and major bleeding (hazard ratio, 1.58 [95% CI, 0.61-4.08]; P=0.34) were comparable between the 2 groups. In this propensity score-matched analysis of the stent arm registry from the HOST-IDEA trial, the Orsiro SES was associated with significantly better outcomes in terms of 1-year target lesion failure, mainly driven by clinically driven target lesion revascularization, than the Coroflex ISAR SES. URL: https://www.clinicaltrials.gov; Unique identifier: NCT02601157.

Ectopic Production of 3,4-Dihydroxybenzoate in Planta Affects Cellulose Structure and Organization.

Lignocellulosic biomass is a highly sustainable and largely carbon dioxide neutral feedstock for the production of biofuels and advanced biomaterials. Although thermochemical pretreatment is typically used to increase the efficiency of cell wall deconstruction, genetic engineering of the major plant cell wall polymers, especially lignin, has shown promise as an alternative approach to reduce biomass recalcitrance. Poplar trees with reduced lignin content and altered composition were previously developed by overexpressing bacterial 3-dehydroshikimate dehydratase (QsuB) enzyme to divert carbon flux from the shikimate pathway. In this work, three transgenic poplar lines with increasing QsuB expression levels and different lignin contents were studied using small-angle neutron scattering (SANS) and wide-angle X-ray scattering (WAXS). SANS showed that although the cellulose microfibril cross-sectional dimension remained unchanged, the ordered organization of the microfibrils progressively decreased with increased QsuB expression. This was correlated with decreasing total lignin content in the QsuB lines. WAXS showed that the crystallite dimensions of cellulose microfibrils transverse to the growth direction were not affected by the QsuB expression, but the crystallite dimensions parallel to the growth direction were decreased by ∼20%. Cellulose crystallinity was also decreased with increased QsuB expression, which could be related to high levels of 3,4-dihydroxybenzoate, the product of QsuB expression, disrupting microfibril crystallization. In addition, the cellulose microfibril orientation angle showed a bimodal distribution at higher QsuB expression levels. Overall, this study provides new structural insights into the impact of ectopic synthesis of small-molecule metabolites on cellulose organization and structure that can be used for future efforts aimed at reducing biomass recalcitrance.

Cyclodextrins-Based Polyrotaxanes: From Functional Polymers to Applications in Electronics and Energy Storage Materials.

The concept of polyrotaxane comes from the rotaxane structure in the supramolecular field. It is a mechanically interlocked supramolecular assembly composed of linear polymer chains and cyclic molecules. Over recent decades, the synthesis and application of polyrotaxanes have seen remarkable growth. Particularly, cyclodextrin-based polyrotaxanes have been extensively reported due to the low-price raw materials, good biocompatibility, and ease of modification. Hence, it is also one of the most promising mechanically interlocking supramolecules for wide industrialization in the future. Polyrotaxanes are widely introduced into materials such as elastomers, hydrogels, and engineering polymers to improve their mechanical properties or impart functionality to the materials. In these materials, polyrotaxane acts as a slidable cross-linker to dissipate energy through sliding or assist in dispersing stress concentration in the cross-linked network, thereby enhancing the toughness of the materials. Further, the unique sliding-ring effect of cyclodextrin-based polyrotaxanes has pioneered advancements in stretchable electronics and energy storage materials. This includes their innovative use in stretchable conductive composite and binders for anodes, addressing critical challenges in these fields. In this mini-review, our focus is to highlight the current progress and potential wider applications in the future, underlining their transformative impact across various domains of material science.

Recent Trends of Recycling and Upcycling of Polymers and Composites: A Comprehensive Review

This review article gathers the most recent recycling technologies for thermoset and thermoplastic polymers. Results about existing experimental procedures and their effectiveness are presented. For thermoset polymers, the review focuses mainly on fibre-reinforced polymer composites, with an emphasis on epoxy-based systems and carbon/glass fibres as reinforcement, due to the environmental concerns of their end-of-life management. Thermal processes (fluidised bed, pyrolysis) and chemical processes (different types of solvolysis) are discussed. The most recent combined processes (microwave, steam, and ultrasonic assisted techniques) and extraordinary recycling attempts (electrochemical, biological, and with ionic liquids) are analysed. Mechanical recycling that leads to the downgrading of materials is excluded. Insights are also given for the upcycling methodologies that have been implemented until now for the reuse of fibres. As for thermoplastic polymers, the most state-of-the-art recycling approach for the most common polymer matrices is presented, together with the appropriate additivation for matrix upcycling. Mechanical, chemical, and enzymatic recycling processes are described, among others. The use of fibre-reinforced thermoplastic composites is quite new, and thus, the most recent achievements are presented. With all of the above information, this extensive review can serve as a guide for educational purposes, targeting students and technicians in polymers recycling.

Flexible and rigid block copolymers from recyclable polyesters

The paper addresses a study on the thermoplastic elastomers (TPE) that can be synthesized using monomers retrieved from the chemically recycled semi-aromatic polyesters, such as terephthalic acid from low value stream recyclable polyethylene terephthalate (rPET). In contrast to PET, because of their physical and mechanical properties, TPEs are often used as an engineering polymer in automotive and consumer goods. The understanding of the crystallization and phase behavior of these materials is crucial to fine-tune the molecular structure and properties. We explore the interplay between the crystallization and phase separation in these materials by performing experiments on model thermoplastic elastomers consisting of polybutylene terephthalate (PBT) and polytetrahydrofuran (PTHF). A common denominator in the synthesis of PBT is terephthalic acid that can be obtained from Dimethyl Terephthalate (DMT) or recycling used PET. We show that by varying the compositions and block length of different blocks, in PBT-PTHF block copolymers, morphological variations from spherulites to dendrites can be induced, which could be captured using optical microscopy. By performing rheological and small angle X-ray scattering studies, we correlate these morphological variations at microscopic length scales, to the chain architecture at nanometer length scales. Our observations reveal that at the higher rigid PBT content, the process of phase separation strongly influences the crystallization kinetics that promotes the lamellar structure of the semi-crystalline polymer, observed at room temperature. On the other hand, in the presence of higher soft block content, the crystal growth occurs with minimal influence of the microphase separation. In broader generality, no morphological differences in the TPEs synthesized using the terephthalic acid from rPET are found. However, when the monomer from rPET is used, enhancement in crystallization rate occurs in the TPEs having similar molar mass and molecular configuration. We attribute the enhanced crystallization rate to the catalyst residues present in the terephthalic acid obtained fom rPET.

Organic Electronics in Flexible Devices: Engineering Strategy, Synthesis, And Application

In recent years, flexible electronics have made significant strides, especially in organic light-emitting diodes, photovoltaics, thin-film transistors, integrated circuits, sensors, and memories. This study investigates the pivotal role of organic electronics in shaping flexible and wearable technology. It explores key aspects such as conductive polymers, small molecule organic semiconductors, and the use of organic dyes and pigments in displays, alongside synthesis techniques like polymerization and vapor deposition. These methods highlight advances in flexibility engineering and integration into wearable devices, enabling innovations like textile-integrated electronics and ultra-thin, skin-like interfaces. The discussion also covers synthesis and fabrication strategies, emphasizing cost-effective, solution-processing techniques for manufacturing electrodes, interconnects, and metal contacts on various flexible substrates. Advanced materials like graphene polymer composites, carbon-nanotube composites, and polymer-ceramic composites are investigated for enhancing stretchability and flexibility in device architectures. Furthermore, the paper examines the evolution of flexible devices, focusing on design strategies for flexibility and stretchability, innovative engineering polymers, composites, and device architectures, including 3D integration. Integration techniques in wearable devices, such as textile integration and skin-like electronics, are discussed, showcasing their transformative potential in applications like health monitoring devices, smart clothing, and wearable displays. Finally, the paper proposed solutions to address challenges such as durability, stability, scalability, and manufacturing efficiency, emphasizing the ongoing quest for improved materials and manufacturing processes. The conclusion underscores the transformative potential of organic electronics, envisioning a new era of wearable and flexible technology seamlessly integrated into daily life, revolutionizing our interactions with electronic devices.

The Right Formula for Acne: Importance of Vehicle Formulation in Tazarotene 0.045% Lotion Design, Application, Tolerability, and Efficacy

The vehicles used for topical dermatological treatments can significantly contribute to treatment effects while also delivering ingredients to maintain skin barrier function and reduce irritation. Tazarotene 0.045% lotion was developed using proprietary polymeric emulsion technology to provide uniform and efficient delivery of the active ingredient as well as improved safety and tolerability compared to higher-dose tazarotene formulations. The lotion vehicle additionally provides rapid and sustained improvements in moisturization and skin barrier function with patient-friendly application and cosmetic properties. Compared with trifarotene 0.005% cream, tazarotene 0.045% lotion demonstrated ∼30% greater spreadability and a lower potential for irritation. In clinical trials and investigator-initiated studies, tazarotene 0.045% lotion demonstrated efficacy in the treatment of facial and truncal acne and improved skin oiliness. Facial acne improvements were similar among study participants grouped by sex, race, ethnicity, or age. In a head-to-head study, efficacy was comparable to tazarotene 0.1% cream with approximately half the rate of treatment-emergent adverse events. Tazarotene 0.045% lotion is a beneficial acne treatment option for patients of varying ages, races, ethnicities, and skin types, delivered in a formulation that can be easily used on the face, back, and chest.

Determination of the flexural properties of additively manufactured polyamide 12 components with antimicrobial titanium dioxide additives

AbstractAntibacterial properties of components are increasingly becoming an important challenge in material development especially in polymer technology. A well‐known additive with which an antibacterial effect can be achieved is the metal oxide titanium dioxide. The aim of this research work was to investigate possible influences on the flexural properties of additively manufactured components resulting from the addition of titanium dioxide as an antimicrobial additive. Compounds with 5 %, 10 % and 15 % titanium dioxide and polyamide 12 as matrix material were produced. Three‐point bending test specimens were fabricated out of these compounds, anaylsed and the results were compared with specimens made of virgin polyamide 12. The investigations show a general loss in ductility compared to the virgin polyamide 12. A comparison of the different titanium dioxide contents shows no clear change in the flexural stress at conventional bending. The flexural strain at break seems to decrease for higher titanium dioxide contents.

Vinyl chloride suspension copolymerization combining click with sol-gel reactions for sustainable antifouling PVC copolymer ultrafiltration membranes

Polymeric ultrafiltration technology, crucial in water treatment and desalination, faces challenges of membrane fouling that compromise performance and shorten the operational lifetime. Traditional polymer ultrafiltration membrane modifications, such as surface adsorption, grafting, and physical blending, have notable limitations including reduced permeability, structural instability, poor compatibility, and additive leakage. To overcome these shortcomings, we present a novel approach based on copolymerization, integrating click chemistry and sol-gel techniques for the preparation of copolymer ultrafiltration membranes. The active sites of sol-gel reaction were introduced into the PVC copolymer backbone through suspension copolymerization. Subsequently, an in-situ modification of resveratrol was carried out within the copolymer casting solution to facilitate sol-gel reaction with PVC skeleton, forming a crosslinking structure during the film-forming process. This approach enhances membrane properties like hydrophilicity, thermal stability, permeability, antifouling capability, and antibacterial adhesion without compromising structural integrity or causing additive leakage. Importantly, the hydrophilicity and permeability are sustained even after prolonged exposure to deionized water and bacterial conditions, respectively. Our research contributes to the advancement of durable and functional ultrafiltration membranes through copolymerization techniques, offering valuable insights to enrich membrane modification strategies for water treatment.

Synthesis and high-temperature energy storage performances of fluorinated polyimides

In light of the increasingly stringent requirements for the applications of light-weight flexible high-temperature-resistant dielectric materials in the fields of aerospace, electronics, and electric vehicles, the imperative lies in the development of dielectric materials with high discharged energy density, enduring temperature resistance and high reliability. This work introduced side-chain trifluoromethyl (–CF3) groups into high-temperature engineering polymer polyimides and conducted comprehensive studies on the breakdown and energy storage capabilities. The introduction of bulky –CF3 substituents reduces the intermolecular interactions, increases the free volume, and suppresses the high-temperature leakage conductance loss by decreasing the formation of intermolecular charge transfer complexes between polymer chains. As a result, the fluorinated polyimides (PFI) with lower dielectric constant exhibit enhanced breakdown strengths (730 MV m−1 at 25 °C; 630 MV m−1 at 150 °C), leading to a high discharged energy density of 3.6 J cm−3 (∼1.7 times of pristine polyimides), alongside a charge-discharge energy efficiency of ∼80% at 150 °C. These findings underscore the great potential of PFI for applications in the field of high-temperature energy storage.

Polymeric Molecular Envelope Technology for Improved Therapeutics Efficacy: A Review.

The review explores the enhancement of therapeutic efficacy through the innovative use of polymeric molecular envelope technology (MET). It delves into the diverse methods employed to achieve superior therapeutic outcomes, shedding light on strategies for improving drug delivery and bioavailability. MET is a promising approach to improve the solubility and bioavailability of poorly water-soluble drugs. This technology involves the use of a molecular envelope of cyclic oligosaccharides called cyclodextrins, which is a supramolecular assembly of amphiphilic molecules that encapsulate and solubilize hydrophobic drug molecules. This can further improve the solubility of the drug by increasing its surface area and reducing its crystallinity. Moreover, MET also protects the drug from degradation and enhances its permeability across biological membranes. Furthermore, the review thoroughly examines the MET, including its methods of preparation, applications in drug encapsulation, and the evaluation of its potential to optimize therapeutic outcomes. By adopting current research and key findings, this review provides valuable insights into the transformative potential of polymeric molecular envelope technology for advancing the field of therapeutics.

Polymer Engineering Enables High Linear Capacity Fiber Electrodes by Microenvironment Regulation.

Unlike bulky and rigid traditional power systems, 1D fiber batteries possess appealing features such as flexibility and adaptability, which are promising for use in wearable electronic devices. However, the performance and energy density fiber batteries are limited by the contradiction between ionic transfer and robust structure of fiber electrodes. Herein, these problems are addressed via polymer engineering to regulate the microenvironment in electrodes, realizing high-linear-capacity thick fiber electrodes with excellent cycling performance. The porosity of the electrodes is regulated using polymer crosslink networks designed with various components, and lithium-ion transfer is optimized through ether-abundant polymer chains. Furthermore, reinforced covalent bonding with carbon nanotube networks is established based on the modified functional groups of polymer networks. The multiscale optimizations of the porous structure, ionic transportation, and covalent bonding network enhance the lithium-ion dynamics property and structural stability. Therefore, ultrahigh linear-capacity fiber electrodes (17.8mAh m-1) can be fabricated on a large scale and exhibit excellent stability (92.8% after 800 cycles), demonstrating obvious superiority among the reported fiber electrodes. Moreover, this study highlights the high effectiveness of polymer regulation in fiber electrodes and offers new avenues for designing next-generation wearable energy-storage systems.

Solution Structure and Dynamics of Hf-Al and Hf-Zn Heterobimetallic Adducts Mimicking Relevant Intermediates in Chain Transfer Reactions.

Cationic cyclometalated hafnocenes [CpPrCpCH2CH2CH2Hf][B(C6F5)4] (4Pr) and [CpiBuCpCH2CH(Me)CH2Hf][B(C6F5)4] (4aiBu and 4biBu) were synthesized from the corresponding [(CpPr)2HfMe][B(C6F5)4] (1Pr) and [(CpiBu)2HfMe][B(C6F5)4] (1iBu) complexes via C-H activation. 4aiBu, 4biBu, and 4Pr, mimicking a propagating M-polymeryl species (M = transition metal) with or without a β-methyl branch on the metalated chains, serve to investigate whether and how the nature of the last inserted olefin molecules changes the structure, stability, and reactivity of the corresponding heterobimetallic complexes, formed in the presence of aluminum- or zinc-alkyl chain transfer agents (CTAs), which are considered relevant intermediates in coordinative chain transfer polymerization (CCTP) and chain shuttling polymerization (CSP) technologies. NMR and DFT data indicate no major structural difference between the resulting heterobridged complexes, all characterized by the presence of multiple α-agostic interactions. On the contrary, thermodynamic and kinetic investigations, concerning the reversible formation and breaking of heterobimetallic adducts, demonstrate that isomer 4aiBu, in which the β-Me is oriented away from the reactive coordination site on Hf, but not 4biBu, having the β-Me pointing in the opposite direction, is capable of reacting with CTAs. Quantification of kinetic rate constants highlights that the formation process is rate limiting and that the nature of the last inserted α-olefin unit modulates transalkylation kinetics. The reaction of 4aiBu, 4biBu, and 4Pr with diisobutylaluminum hydride (DiBAlH) allows the interception and characterization of new heterobinuclear and heterotrinuclear species, featuring both hydride and alkyl bridging moieties, which represent structural models of elusive intermediates in CCTP and CSP processes, capturing the instant when an alkyl chain has just transferred from a transition metal to a main group metal, while the two metals remain engaged in a single heterobimetallic intermediate.

Sir Geoffrey Allen. 29 October 1928—15 March 2023

Sir Geoffrey Allen was first and foremost a very fine scientist, highly respected, especially for his expertise in polymer science and technology. Over time he built up an extensive network of scientific know-how globally, establishing on-going relationships with many key scientists that enabled him to provide vision and leadership for the scientific community in academia and the world of business. Allen's ability to give a succinct and clear summary of an issue, his view and the reasoning behind his view were remarkable. He was very supportive of younger scientists, particularly when he perceived talent, and encouraged them. He devoted much of his free time to promoting science and technology in various forums but especially that of young people, and was particularly good at motivating people, being extremely effective at all levels. He was great confidence builder in any situation.

Impact of infill density on morphology and mechanical properties of 3D printed ABS/CF-ABS composites using design of experiments

Metal Extrusion (MEX) is a leading 3D printing technology for polymers, enabling intricate designs and personalized products in various applications. The current study evaluate how infill density affects the tensile, flexural, compressive, Izod impact and fracture behaviour of Acrylonitrile Butadiene Styrene (ABS) and Carbon Fiber Reinforced-Acrylonitrile Butadiene Styrene (CF-ABS) specimens manufactured using the MEX method. Different infill densities of 20, 40, 60 and 80 % are used in the production of honeycomb infill pattern samples for investigating the mechanical as well as fracture behaviour of MEX ABS/CF-ABS components. The experimental runs of fabricated composites were tested using a digital Izod impact tester and servo-controlled hydraulic universal testing machine, following ASTM standard procedures. The experimental findings show that CF-ABS specimens with an 80 % infill density and honeycomb fill pattern showed significant improvements in tensile strength, modulus, yield strength and elongation. The flexural strength (64.74 %), flexural modulus (209.15 %), compressive strength (125.21 %), compressive modulus (108.34 %) and impact strength (38.91 %) of these specimens are comparable to those of 3D printed ABS specimens and other infill densities. The research shows that precise management of processing variables can greatly improve the mechanical properties of 3D-printed ABS samples, providing valuable insights for a range of applications.

Tribological Performance and Enhancing Mechanism of 3D Printed PEEK Coated with In Situ ZIF-8 Nanomaterial.

Polyether ether ketone (PEEK) is esteemed as a high-performance engineering polymer renowned for its exceptional mechanical properties and thermal stability. Nonetheless, the majority of polymer-based lubricating materials fail to meet the contemporary industrial demands for motion components regarding high speed, heavy loading, temperature resistance, and precise control. Utilizing 3D printing technology to design and fabricate intricately structured components, developing high-performance polymer self-lubricating materials becomes imperative to fulfill the stringent operational requirements of motion mechanisms. This study introduces a novel approach employing 3D printing technology to produce PEEK with varying filling densities and conducting in situ synthesis of zeolitic imidazolate framework (ZIF-8) nanomaterials on its surface to enhance PEEK's frictional performance. The research discusses the synthetic methodology, characterization techniques, and tribological performance evaluation of in situ synthesized ZIF-8 nanomaterials on PEEK surfaces. The findings demonstrate a significant enhancement in frictional performance of the composite material under low-load conditions, achieving a minimum wear rate of 4.68 × 10-6 mm3/N·m compared to the non-grafted PEEK material's wear rate of 1.091 × 10-5 mm3/N·m, an approximately 1.3 times improvement. Detailed characterization and analysis of the worn surface of the steel ring unveil the lubrication mechanism of the ZIF-8 nanoparticles, thereby presenting new prospects for the diversified applications of PEEK.

Searching for the Achilles' Heel of Urethane Linkage-An Energetic Perspective.

A sudden increase in polyurethane (PU) production necessitates viable recycling methods for the waste generated. PU is one of the most important plastic materials with a wide range of applications; however, the stability of the urethane linkage is a major issue in chemical recycling. In this work, termination reactions of a model urethane molecule, namely methyl N-phenyl carbamate (MPCate), are investigated using G3MP2B3 composite quantum chemical method. Our main goal was to gain insights into the energetic profile of urethane bond termination and find an applicable chemical recycling method. Hydrogenation, hydrolysis, methanolysis, peroxidation, glycolysis, ammonolysis, reduction with methylamine and termination by dimethyl phosphite were explored in both gas and condensed phases. Out of these chemicals, degradation by H2, H2O2 and CH3NH2 revealed promising results with lower activation barriers and exergonic pathways, especially in water solvation. Implementing these effective PU recycling methods can also have significant economic benefits since the obtained products from the reactions are industrially relevant substances. For example, aniline and dimethyl carbonate could be reusable in polymer technologies serving as potential methods for circular economy. As further potential transformations, several ionizations of MPCate were also examined including electron capture and detachment, protonation/deprotonation and reaction with OH-. Alkaline digestion against the model urethane MPCate was found to be promising due to the relatively low activation energy. In an ideal case, the transformation of the urethane bond could be an enzymatic process; therefore, potential enzymes, such as lipoxygenase, were also considered for the catalysis of peroxidation, and lipases for methanolysis.

Room temperature 3D printing of high-temperature engineering polymer and its nanocomposites with porosity control for multifunctional structures

There is an increasing demand for the development of additive manufacturing techniques that support diverse materials with specific properties and performance characteristics. Engineering polymers are a type of high-performance material with lightweight, strong, and heat resistant. These properties enable replacing more dense materials, such as metals, and make them essential for application in various high-tech industries. Polyamide-imide (PAI) is an advanced engineering polymer with exceptional mechanical properties and thermal stability. However, due to the high glass transition temperature (Tg), the additive manufacturing of PAI 3D structures has not been realized through existing technologies. This study demonstrates room-temperature 3D printing for the PAI and PAI-based functional nanocomposite. Moreover, through a designed post-process drying procedure to control porosity, it is possible to enhance 3D structures' mechanical properties and functionality. The nanocomposite 3D systems exhibit a tensile strength of up to 105 MPa and Tg of 295 °C with aramid nanofibers, and an electrical conductivity of 200 S/m at 250 °C with carbon nanotubes. Given the high performance of printed nanocomposites with designed processes, we explore the potential and expended usage of more robust and lightweight polymer structures featuring diverse functionality for high-tech industries such as aerospace, air mobility, and semiconductor packaging.

Molecularly imprinted ratiometric electrochemical sensor based on 3D-1D MoS2@CNTs hetero-nanoflower for selective detection of trimethoprim

Trimethoprim (TMP) is a broad-spectrum antibiotic that is frequently found residue in the environment and food. An innovative electrochemical sensor was proposed for the detection of trimethoprim with high selectivity, sensitivity and reproducibility through the integration of the flower-like MoS2@CNTs heterostructure as substrate, molecular imprinted polymer (MIP) technology as recognition, and the ratiometric strategy between trimethoprim and ferrocene (Fc) for quantitative. The recognition reaction of TMP by MIP-MoS2@CNTs sensor was assumed as an irreversible electrochemical oxidation reaction controlled by a combination of adsorption-diffusion process with two electrons and protons. With the incorporation of Fc during detection, a satisfying linear relationship of ITMP/IFc and the concentration of TMP was achieved, indicating a detection concentration ranging from 50 to 3000 nmol·L−1 with a detection limit of 27.01 nmol·L−1. In addition, the MoS2@CNTs MIP ratiometric sensor exhibited good stability for 20 days and excellent reproducibility with a relative standard deviation of 1.06 %, which was lower than 3.89 % of single signal. The practical feasibility of the sensor was detected in water samples with recovery rates of 98.62 ∼ 107.47 % and fish samples with recovery rates of 98.93 ∼ 105.45 %. Overall, the developed MIP ratiometric sensor provides a versatile system with easy operation and great potential for detecting small hazardous molecules in the environment and food products.

Editorial: Polymers in geotechnical and geoenvironmental engineering

Editorial: Polymers in geotechnical and geoenvironmental engineering