Solvent Swelling Research Articles

Imidazole ionic liquid effects on coal swelling behavior and pyrolysis characteristics: Experiment and molecular simulation

In view of low-rank coal conventional swelling solvent large pollution and the clean efficient utilization of coal, the effects of imidazole ionic liquid (IL) pretreatment with different anion groups as green solvent on coal thermal expansion and pyrolysis performance were investigated. IL interacts with coal molecules, destroying the hydrogen bonds, resulting coal expansion. Different anion groups have different modification effects, [Bmim]Cl has the best swelling effect, which is 17.37 % higher than raw coal, and the best modification time is 24 h. In addition, IL modification has a catalytic effect on coal pyrolysis, which can significantly reduce the maximum weight loss temperature and increase tar content. Coal solvent pretreatment provides a good theoretical basis for application of swelling and pyrolysis. The reduction of thermochemical reaction temperature not only reduces the content of heavy groups in pyrolysis products, but also provides new ideas for carbon emission reduction.

Atmospheric pressure atomic layer deposition for in-channel surface modification of PDMS microfluidic chips

Polydimethylsiloxane (PDMS) is one of the materials of choice for the fabrication of microfluidic chips. However, its broad application is constrained by its incompatibility with common organic solvents and the absence of surface anchoring groups for surface functionalization. Current solutions involving bulk-, ex-situ surface-, and in-situ liquid phase modifications are limited and practically demanding. In this work, we present a simple, novel strategy to deposit a metal oxide nano-layer on the inside of bonded PDMS microfluidic channels using atmospheric pressure atomic layer deposition (AP-ALD). Using three important classes of microfluidic experiments, i.e., (i) the production of micron-sized particles, (ii) the cultivation of biological cells, and (iii) the photocatalytic degradation in continuous flow chemistry, we demonstrate that the metal oxide nano-layer offers a higher resistance against organic solvent swelling, higher hydrophilicity, and a higher degree of further functionalization of the wall. We demonstrate the versatility of the approach by not only depositing SiOx nano-layers, but also TiOx nano-layers, which in the case of the flow chemistry experiment were further functionalized with gold nanoparticles through the use of AP-ALD. This study demonstrates AP-ALD as a tool to broaden the applicability of PDMS devices.

Characterization of Natural Zeolite Synthesized by Dealumination and Desilication Method

Delamination and desilication are two methods used in the hierarchical synthesis of zeolites. This process is important for industrial applications, particularly in synthesizing natural zeolites due to their abundance. For instance, Lampung, Indonesia, has abundant natural zeolites. The synthesis process of natural zeolite can be simplified using the solvent swelling mechanism. The swelling solvent mechanism combines the dealumination and desilication methods into one process, making it advantageous to use natural zeolites as raw materials for manufacturing hierarchical zeolites on an industrial scale. The sample used in this study was Natural Zeolite Lampung (NZL), and the resulting product was characterized as NZL Swelling. In this study, only two characterization analyses were selected to test the reliability of the dealumination and desilication methods simultaneously in one process, namely XRD and BET.

Development of a new type of highly effective etchant solution for glue residue in wafer-level packaging process

We synthesize an etchant solution designed to remove polydimethylsiloxane (PDMS) residues from semiconductor wafers during wafer-to-wafer processing in advanced semiconductor packaging (AVP). The etchant solution is produced by combining hexane, a nonpolar swelling solvent, with tetrabutylammonium fluoride (TBAF), a fluorine-based compound, to enhance PDMS etching. We evaluate the etching rate of PDMS using various solvent mixtures, including 1-vinyl-2-pyrrolidone, 1-methyl-2-pyrrolidone, 1-ethyl-2-pyrrolidone, and 1-octyl-2-pyrrolidone (NOP), with different concentrations of TBAF (1.0–5.0 wt%). Notably, NOP, which contains octyl groups, demonstrates the highest PDMS etching rate, particularly when combined with 70.0 wt% hexane. The optimized solution, F3-NOP/H70, achieves an etching rate of 85.7 μm/min. Further testing confirms that the F3-NOP/H70 solution effectively removes PDMS residues from wafer surfaces without damaging dielectric layers, such as the photosolder resist and photosensitive polyimide. These results indicate that the F3-NOP/H70 solution efficiently dissolves and removes PDMS residues and preserves the integrity of adjacent wafer components, making it a promising candidate for AVP applications. This study emphasizes the importance of selecting appropriate solvent systems for residue removal in semiconductor manufacturing and offers a practical solution to enhance device quality and reliability. This approach can potentially be applied at various stages of semiconductor processing, where residue management is essential.

Integration of acoustic micromixing with cyclic olefin copolymer microfluidics for enhanced lab-on-a-chip applications in nanoscale liposome synthesis

The integration of acoustic wave micromixing with microfluidic systems holds great potential for applications in biomedicine and lab-on-a-chip technologies. Polymers such as cyclic olefin copolymer (COC) are increasingly utilized in microfluidic applications due to its unique properties, low cost, and versatile fabrication methods, and incorporating them into acoustofluidics significantly expands their potential applications. In this work, for the first time, we demonstrated the integration of polymer microfluidics with acoustic micromixing utilizing oscillating sharp edge structures to homogenize flowing fluids. The sharp edge mixing platform was entirely composed of COC fabricated in a COC-hydrocarbon solvent swelling based microfabrication process. As an electrical signal is applied to a piezoelectric transducer bonded to the micromixer, the sharp edges start to oscillate generating vortices at its tip, mixing the fluids. A 2D numerical model was implemented to determine the optimum microchannel dimensions for experimental mixing assessment. The system was shown to successfully mix fluids at flow rates up to 150 µl h−1 and has a modest effect even at the highest tested flow rate of 600 µl h−1. The utility of the fabricated sharp edge micromixer was demonstrated by the synthesis of nanoscale liposomes.

Discrimination of Xylene Isomers by Precisely Tuning the Interlayer Spacing of Reduced Graphene Oxide Membrane.

Separating xylene isomers is a challenging task due to their similar physical and chemical properties. In this study, we developed a molecular sieve incorporating a reduced graphene oxide (rGO) membrane for the precise differentiation of xylene isomers. We fabricated GO membranes using a vacuum filtration technique followed by thermal-induced reduction to produce rGO membranes with precisely controllable interlayer spacing. Notably, we could finely tune the interlayer spacing of the rGO membrane from 8.0 to 5.0 Å by simply varying the thermal reduction temperature. We investigated the reverse osmosis separation ability of the rGO membranes for xylene isomers and found that the rGO membrane with an interlayer spacing of 6.1 Å showed a high single component permeance of 0.17 and 0.04 L m-2 h-1 bar-1 for para- and ortho-xylene, respectively, exhibiting clear permselectivity. The separation factor reached 3.4 and 2.8 when 90:10 and 50:50 feed mixtures were used, respectively, with permeance 1 order of magnitude higher than that of current state-of-the-art reverse osmosis membranes. Additionally, the membrane showed negligible permeance and selectivity decay even after continuous operation for more than 5 days, suggesting commendable membrane resistance to solvent swelling and operating pressure.

Interface Interaction of Waste Rubber–Asphalt System

Asphalt pavement construction is a large-volume project, with the ability to recycle the industrial waste and reduce carbon emissions. Rubber-modified asphalt is a carbon-neutralized asphalt-based material, facilitating the recycling of waste rubber materials and improving the road performance of the asphalt mixture. To evaluate the interface interaction of the rubber–asphalt system and its effect on the viscosity characteristics of rubber-modified asphalt, the contact properties of rubber particles in asphalt were analyzed on a microscopic level. Rubber swelling tests and solvent elution tests were conducted on the rubber–asphalt system under different preparation conditions. The swelling ratio, degradation ratio, and swelling–degradation ratio were proposed to evaluate the interface interaction. The results show that the interface interaction of the rubber–asphalt system can be divided into the following three stages: swelling, effective degradation, and over-degradation. The degree of swelling is mainly affected by the content and size of the rubber particles and it is physically condensed, while the degradation is mainly affected by the preparation temperature and preparation time. The effective interface interaction greatly affects the viscosity with the building of the stable three-dimensional network structure. The stronger the interface interaction, the greater the viscosity of the rubber-modified asphalt, except for the 25% content of rubber particles. The gel film will be generated on the surface of the rubber particles throughout the swelling and effective degradation, increasing the viscosity of the rubber-modified asphalt.

Effect of reduced graphene oxide on vulcanization of polydimethylsiloxane composites

AbstractThis research aims to investigate the effect of reduced graphene oxide (rGO) on the kinetics of addition vulcanization in polydimethylsiloxane (PDMS) elastomers. For this purpose, the synthesis of graphene oxide (GO) and silane‐grafted GO followed by chemical reduction of particles was conducted to prepare rGOs with different surface chemistry. Particles were characterized by Fourier transform infrared spectroscopy, Raman spectroscopy, x‐ray diffraction, scanning electron microscopy, and energy‐dispersive x‐ray analysis. Composites of PDMS containing these particles were prepared by solution mixing, and vulcanization of composites was investigated using differential scanning calorimetry. Results showed that the rate and degree of vulcanization reaction increase up to a critical concentration of particles and then decrease afterward. This behavior was attributed to the catalytic effect of chemical groups on the surface of rGOs, whereas the reverse behavior above the critical concentration was correlated to the immobilization of trapped rubber in the network of particles. Grafting graphene oxide by a long alkyl‐chain silane covered these chemical groups, suppressed the catalytic effect, improved the dispersion of particles, and shifted the critical concentration lower. The critical concentration was correlated to the electrical percolation threshold of particles and confirmed by the solvent swelling method. It was also shown that rGO can itself act as the catalyst for the vulcanization of PDMS with no need for platinum. As the dynamic‐mechanical‐thermal analysis showed, the PDMS composites containing 0.75 wt% of particles did not vulcanize properly. However, composites containing fewer particles were vulcanized.Highlights Reduced graphene oxide affects additional vulcanization of PDMS. Below a critical loading, rGO accelerates vulcanization by a catalytic effect. Above critical loading, rGO decelerates vulcanization by a networking effect. Surface groups of rGO control catalytic and networking mechanisms. Silane modification of rGO affects interfacial behavior, thus critical loading.

Multifunctional bionanohybrids of graphene oxide/β-cyclodextrin for applications in methylene blue adsorption, solvent response, and smart light-driven

In this study, a multifunctional graphene oxide/β-cyclodextrin bionanohybrids (BWGO) was prepared successfully. The structure, morphology, adsorption capacity, solvent response, and light-driven properties of the BWGO were systematically investigated through the in-situ formation of an asymmetric gradient structure. The maximum adsorption value of BWGO based on bio-nanohybrids was 81.27 mg·g−1 for methylene blue (MB), which fitted the Langmuir isotherm in accordance with the pseudo-secondary kinetic model. Additionally, the host–guest interaction model of between BWGO and MB (in ratios of 1:1 or 1:2) was proposed by ROESY. Remarkably, the BWGO exhibited not only unique and exceptional responses to organic hazard solvents, self-driven, and photothermal responses, but also demonstrated controllable object loading and shape memory useful for soft grasping. More importantly, the related mechanisms of adsorption and behaviors driven by multiple stimuli (solvent, light) were elucidated through the host–guest interaction, wrinkled structure, gradient solvent swelling effects, and conformational changes in the macromolecular chain. This work not only introduces the multifunctional bionanohybrid materials with a wrinkled structure for the adsorption of organic dyes, but also opens avenues for potential applications in smart windows, soft grasping, and biomimetic industrial materials.

Amphiphilic polymer Co-networks based on cross-linked tetra-PEG-b-PCL star block copolymers

A new class of AB4-type amphiphilic polymer co-networks (ACN) was prepared by hetero-complementary 2-(4-nitrophenyl)-benzoxazinone/amine end group cross-linking chemistry in dimethyl sulfoxide (DMSO). For this purpose, a well-defined star block copolymer (tetra-PEG-b-PCL) consisting of a hydrophilic tetra-arm PEG core (Mn ∼ 5 kg mol−1) and hydrophobic PCL wings with a total molar mass of Mn ∼ 10 kg mol−1 was synthesized by ring-opening polymerization (ROP). This tetra-PEG-b-PCL star block copolymer was functionalized either with 2-(4-nitrophenyl)-benzoxazinone or with amino terminal groups. The ACN synthesis was carried out by conversion of these two star block copolymers. The overlap concentration of c* ∼76 g L−1 determined by viscosity measurements of both stars showed no significant temperature dependence. The network syntheses carried out at different concentrations (0.5 c* to 2.5 c*) resulted in conversion degrees in the range of p ≈ 95 % or higher as detected by HR MAS NMR spectroscopy. As in previous work on the synthesis of A4B4 networks using the same cross-linking chemistry, deviations from the expected network structure (increased proportion of double links between two stars) were detected also here by multi quantum NMR spectroscopy. The expected environmentally sensitive behavior of the ACNs was confirmed in terms of their equilibrium swelling in solvents of different quality to PEG and PCL. The scaling of the swelling and viscoelasticity data as a function of preparation concentration showed deviations from the expectations of a perfectly cross-linked star polymer network. Finally, a two-step gelation process was observed by rheology at 30 °C in DMSO, which is related to associations between the 2-(4-nitrophenyl)-benzoxazinone groups surrounded by PCL blocks that become apparent on the time scale of rheology when the molar mass is increased as a result of cross-linking.

Intrinsically microporous polyimide membranes with synergistic aromatic and alicyclic linking groups for efficient molecular separation

Polymers of intrinsic microporosity (PIMs) are widely recognized for having great potential in reforming membrane technology for molecular separation within organic solvents, due to their rich and appropriate pore structures with a size < 2 nm. However, the swelling in organic solvents has a significant effect on their pore structures due to the amorphous and linear nature, resulting in the permeability and selectivity performances of developed PIM membranes being far from ideal. In this work, we synthesized an advanced polyimide of intrinsic microporosity by integrating a Tröger’s base (TB) structure with an synergistic structure of aromatic (naphthalenediimide, NDI) and alicyclic (bicyclooctenediimide, BCODI) linking groups. The TB with a rigid and twisted structure was used to furnish a basis for inhibiting chain packing for high overall free volume. The ultra-rigid NDI units maintained such a tailored high free volume and provided superior solvent resistance. The relatively flexible and polar BCODI units promoted local chain mobility to tailor uniform pore size distribution and increased affinity for polar solvents. The innovative design fostered the formation of stable, uniform, and highly solvent-accessible intrinsic micropores. The prepared TFC membrane exhibited good organic solvent separation capabilities, achieving an ethanol permeance of 7.6 L m-2 h−1 bar−1 and a low molecular weight cut-off (MWCO) of approximately 470 Da. This work contributes significantly to the strategic design of PIMs for preparing high-performance membranes for realistic chemical-related separation application scenarios.

Introducing Optical Nonlinearity in PDMS Using Organic Solvent Swelling

The feasibility of introducing optical nonlinearity in poly-dimethyl siloxane (PDMS) using organic solvent swelling was investigated. The third-order nonlinear refraction and absorption properties of the individual materials, as well as the PDMS/solvent compounds after swelling were characterized. The well-established Z-scan technique served as characterization method for the nonlinear properties under picosecond pulsed laser excitation at a 532 nm wavelength. These experiments included investigations on the organic solvents nitrobenzene, 2,6-lutidine, and toluene, which showed inherent optical nonlinearity. We showed that nitrobenzene, one of the most well-known nonlinear optical materials, has proven suboptimal in this context due to its limited swelling effect in PDMS and comparatively high (non)linear absorption, resulting in undesirable thermal effects and potential photo-induced damage in the composite material. Toluene and 2,6-lutidine not only exhibited lower absorption compared to nitrobenzene but also show a more pronounced swelling effect in PDMS. The incorporation of toluene caused a weight change of up to 116% of PDMS, resulting in substantial nonlinear optical effects, reflected in the nonlinear refractive index of the PDMS/toluene composite n2=3.1×10−15 cm2/W.

Quantifying Doping Efficiency to Probe the Effects of Nanoscale Morphology and Solvent Swelling in Molecular Doping of Conjugated Polymers

Quantifying Doping Efficiency to Probe the Effects of Nanoscale Morphology and Solvent Swelling in Molecular Doping of Conjugated Polymers

Chitosan Biocomposites with Variable Cross-Linking and Copper-Doping for Enhanced Phosphate Removal.

The fabrication of chitosan (CH) biocomposite beads with variable copper (Cu2+) ion doping was achieved with a glutaraldehyde cross-linker (CL) through three distinct methods: (1) formation of CH beads was followed by imbibition of Cu(II) ions (CH-b-Cu) without CL; (2) cross-linking of the CH beads, followed by imbibition of Cu(II) ions (CH-b-CL-Cu); and (3) cross-linking of pristine CH, followed by bead formation with Cu(II) imbibing onto the beads (CH-CL-b-Cu). The biocomposites (CH-b-Cu, CH-b-CL-Cu, and CH-CL-b-Cu) were characterized via spectroscopy (FTIR, 13C solid NMR, XPS), SEM, TGA, equilibrium solvent swelling methods, and phosphate adsorption isotherms. The results reveal variable cross-linking and Cu(II) doping of the CH beads, in accordance with the step-wise design strategy. CH-CL-b-Cu exhibited the greatest pillaring of chitosan fibrils with greater cross-linking, along with low Cu(II) loading, reduced solvent swelling, and attenuated uptake of phosphate dianions. Equilibrium and kinetic uptake results at pH 8.5 and 295 K reveal that the non-CL Cu-imbibed beads (CH-b-Cu) display the highest affinity for phosphate (Qm = 133 ± 45 mg/g), in agreement with the highest loading of Cu(II) and enhanced water swelling. Regeneration studies demonstrated the sustainability and cost-effectiveness of Cu-imbibed chitosan beads for controlled phosphate removal, whilst maintaining over 80% regenerability across several adsorption-desorption cycles. This study offers a facile synthetic approach for controlled Cu2+ ion doping onto chitosan-based beads, enabling tailored phosphate oxyanion uptake from aqueous media by employing a sustainable polysaccharide biocomposite adsorbent for water remediation by mitigation of eutrophication.

Improving interfacial bonding strength between epoxy and PE-based wood plastic composites by micro-riveting

In this paper, we proposed a micro-riveting method using the wood fibers in the wood plastic composites (WPC) to effectively enhance the interfacial bonding strength between the epoxy coating and polyethylene (PE) -based WPC. The WPC surface with wood fibers partially embedded in the PE matrix was prepared using a simple solvent swelling and polishing method. Epoxidized Cardol having a long and hydrophobic chain was modified on the surface of the exposed wood fibers to improve the water-resistance and chemical reactivity of the wood fiber surface. Fourier transforms infrared (FT-IR) spectra, X-ray photoelectron spectroscopy (XPS), contact angle, confocal microscopy, and scanning electron microscope (SEM) have been used to characterize the composition and morphology of the surface structures. A pull-off test has been used to evaluate the interface bonding strength, which increased from 1.88 to 5.27 MPa. This constitutes the highest performance among all the non-plasma surface treatment reports (30 % higher than the highest bonding strength reported in the literature and comparable to plasma-based surface treatments). The epoxy-WPC interface showed excellent water resistance after immersing in sodium chloride (NaCl) solution (3.5 wt%) for 60 days. The proposed micro-riveting method is of high significance for WPC and may contribute to the interface adhesion enhancement of other polymer composites.

Structural Homogeneity of Macromolecular Networks by End-to-End Click Chemistry between Discrete Tetrahedral Star Macromolecules.

Cross-linking via the end-to-end click chemistry of multiarm star polymers creates polymer networks with minimal inhomogeneities. Although it has been suggested that the mechanical and swelling properties of such networks depend on the absence of defects, the structural details of homogeneous networks created by this method have not yet been studied at the molecular level. Here, we report the synthesis of discrete tetrahedral star macromolecules (dTSMs) composed of polylactide (PLA) arms with discrete molecular weight and sequence. Polymer networks prepared by 4 × 4 cross-linking by Cu-free strain-promoted cyclooctyne-azide click chemistry (SPAAC) reaction exhibited a high degree of swelling (>40 fold by weight) in solvents without sacrificing mechanical robustness (elastic modulus >4 kPa). The structural details of the networks were investigated by network disassembly spectrometry (NDS) using MALDI-TOF mass spectrometry. By implementing a cleavable repeating unit in the discrete PLA arms of dTSM in a sequence-specific manner, the networks could be disassembled into fragments having discrete molecular weights precisely representing their connectivity in the network. This NDS analysis confirmed that end-to-end click reactions of dTSM networks resulted in the formation of a homogeneous network above the critical concentration (∼10 w/v%) of building blocks in the solution.

Quantification of natural rubber blends by reflection/reflectance infrared and confocal Raman spectroscopy: a comparison of statistical methods.

The blend of butadiene and acrylonitrile copolymer (NBR) with natural poly-cis-isoprene (NR) shows increased resistance to swelling in solvents in comparison to the individual components. In aerospace, NBR rubber is used as thermal protection for rockets and shall not contain other polymers, even in low contents, otherwise, it can affect the protection performance and rocket safety by causing detachment of the elastomer/propellant interface; therefore, this investigation presents methodologies to determine the NR/NBR contents. This study explores different analytical techniques, such as Raman spectroscopy and Fourier transform infrared (FTIR) spectroscopy, in the mid-infrared (MIR) by reflection and in the near-infrared by reflectance (NIRA) modes, Furthermore, quantification strategies by univariate, bivariate and multivariate (chemometric) models are evaluated and compared. A proposed methodology, based on multivariate Raman microscopy with partial least squares regression (PLS), showed high linearity (R2 > 0.99) and low error (< 0.82 %). The validation of FT-MIR data for the CH3, which presented lower error (1.3%) than vinylidene band (6%), showed that both methodologies (reflection and NIRA reflectance) can be used for the quantification of NR in NR/NBR. These results constitute a contribution to the state of the art in researching industrial and aerospace elastomeric applications.

Reversible thermochromic fibers with excellent elasticity and hydrophobicity for wearable temperature sensors.

Color-changing fibers, which can intuitively convey information to the human eye, can be used to facilely add functionality to various types of clothing. However, they are often expensive and complex, and can suffer from low durability. Therefore, in this study, we developed highly elastic and hydrophobic thermochromic fibers as wearable temperature sensors using a simple method that does not require an electric current. A thermochromic pigment was embedded inside and outside hydrophobic silica aerogel particles, following which the thermochromic aerogel was fixed to highly elastic spandex fibers using polydimethylsiloxane as a flexible binder. In particular, multi-strand spandex fibers were used instead of single strands, resulting in the thermochromic aerogels penetrating the inside of the strands upon their expansion by solvent swelling. During drying, the thermochromic aerogel adhered more tightly to the fibers by compressing the strands. The thermochromic fiber was purple at room temperature (25 °C), but exhibited a two-stage color change to blue and then white as the temperature increased to 37 °C. In addition, even after 100 cycles of tension-contraction at 200%, the thermochromic aerogel did not detach and was strongly attached to the fiber. Additionally, it was confirmed that color change due to temperature was stable even after exposure to 1 wt% NaCl (artificial sweat) and 0.1 wt% detergent solutions. The developed thermochromic fiber therefore exhibited excellent elasticity and hydrophobicity, and is expected to be widely utilized as an economical wearable temperature sensor as it does not require electrical devices.

Methyl methacrylate-modified polystyrene microspheres: an effective strategy to enhance the fluorescence of Eu-complexes.

The in vitro detection applications of europium complex-doped microspheres mainly rely on strong fluorescence intensity and a well-defined morphology. In this work, using methyl methacrylate-modified polystyrene microspheres has been proven an effective strategy to enhance the fluorescence and morphology of Eu-complexes. The experimental results showed that the modification resulted in the formation of a porous structure within the polystyrene microspheres, enhancing the doping uniformity and facilitating a more significant accumulation of fluorescent molecules. Furthermore, because of their encapsulation ability, microspheres efficiently confine the fluorescent molecules within them. In addition, the nano-scale porous structure endowed the microspheres with enhanced properties without compromising solvent swelling capability, thereby significantly boosting the fluorescence performance of porous PSMMA. In lateral flow immunoassays (LFIAs), PSMMA-Eu microspheres were effectively utilized to detect fentanyl with exceptional sensitivity by capitalizing on these benefits, capable of detecting concentrations as low as 0.10 ng mL-1. This technology has significant potential for rapid point-of-care screening and clinical applications.

Nafion-Based Quasi-Solid-State Polymer Electrolyte for Lithium-Sulfur Batteries

Lithium-sulfur batteries are considered a strong contender for next-generation high-energy battery systems given their high gravimetric energy density. However, this battery chemistry is still facing challenges such as the polysulfide shuttle effect caused by the high solubility of long-chain lithium polysulfides (Li2Sn) resulting in active material loss and compromised cycle life. Solid-state polymer electrolytes (SPEs) represent a promising pathway to address this issue by preventing the formation and transport of these undesirable polysulfide intermediates.1,2 Moreover, the application of flexible polymer electrolytes promotes safe high energy batteries for smart textiles.In this study, single lithium-ion conducting solid polymer electrolytes (SLIC-SPEs) based on lithiated Nafion membrane have been investigated, utilizing the chemical and thermal stability of this kind of ionomers. Among others, a mixture of ethylene carbonate (EC) and propylene carbonate (PC) was tested as organic aprotic swelling solvent offering advantageous characteristics such as great chemical stability and high ion mobility while avoiding phase separation issues and undesired leaching.Sulfur-infiltrated ultramicroporous carbon composite cathodes were utilized in combination with the investigated SLIC-SPEs, facilitating a quasi-solid-state lithium-sulfur full cell with carbonate-solvent compatibility and high active material utilization.3 Electrochemical performance of the full cell was investigated elaborately and compared with a reference system using solely the liquid EC:PC solvent. While rapid capacity fading can be observed for the liquid electrolyte cell, an enduring high capacity is found in the lithiated-Nafion system. For better understanding of these effects, cycling analysis was accompanied by implementing impedance spectroscopy upon galvanostatic cycling. The electrochemical characterization indicates the formation of a stable film and high degree of reversibility during cycling of the lithiated-Nafion cell whereas an increased film resistance due to sulfur cross-over and electrolyte decomposition was observed within the liquid electrolyte system.(1) Z. Li, W. Lu, N. Zhang, Q. Pan, Y. Chen, G. Xu, D. Zeng, Y. Zhang, W. Cai, M. Yang, J. Mater. Chem. A 2018, 6 (29), 14330-14338.(2) X. Hao, H. Wenren, X. Wang, X. Xia, J. Tu, J. Colloid Interface sci. 2020, 558, 145-154,(3) M. Nojabaee, B. Sievert, M. Schwan, J. Schettler, F. Warth, N. Wagner, B. Milow, K. A. Friedrich, J. Mater. Chem. A 2021, 9 (10), 6508-6519,