Selection Of Binders Research Articles

The Effects of Reclaimed Asphalt Pavement Modification on the Delta Tc Parameter for PG58-XX and PG64-XX Asphalt Binders

The use of reclaimed asphalt pavement (RAP) in asphalt mixtures has increased due to its economic and environmental benefits. However, RAP integration can negatively impact the durability and performance of asphalt binders, particularly at low temperatures. This study evaluates the effects of RAP modification on the ΔTC parameter, a key indicator of binder brittleness and resistance to non-load-related cracking, focusing on PG XX-34 and PG XX-28 grades commonly used in Kansas. Laboratory testing was conducted on virgin and RAP binders subjected to Rolling Thin-Film Oven (RTFO) and Pressure Aging Vessel (PAV) aging. Blended binders were prepared with RAP replacement levels of 15%, 25%, and 40%. The critical temperatures TC,m, TC,S, and ΔTC values were calculated using data from Bending Beam Rheometer (BBR) testing. The results showed that increasing RAP content generally led to more negative ΔTC values, indicating reduced relaxation capacity and higher susceptibility to thermal cracking. RAP source variability also affected performance, with some sources causing more severe deterioration than others. These findings highlight the limitations of conventional linear blending assumptions and underscore the need for improved RAP characterization in binder selection. The study recommends limiting RAP replacement to 25% unless the RAP source demonstrates favorable properties, incorporating ΔTC thresholds (−2.5 °C and −5.0 °C) into binder specifications, and further investigating RAP–virgin binder interactions to enhance long-term pavement performance. The findings support the potential adoption of ΔTC as a specification criterion for binder evaluation, helping agencies like the Kansas Department of Transportation (KDOT) balance binder durability and RAP use.

Selection of binder on SiO2-based thick film for radiative cooling applications

Selection of binder on SiO2-based thick film for radiative cooling applications

Review: Overview of Organic Cathode Materials in Lithium-Ion Batteries and Supercapacitors

Organic materials have emerged as promising candidates for cathode materials in lithium-ion batteries and supercapacitors, offering unique properties and advantages over traditional inorganic counterparts. This review investigates the use of organic compounds as cathode materials in energy storage devices, focusing on their application in lithium-ion batteries and supercapacitors. The review covers various types of organic materials, organosulfur compounds, organic free radical compounds, organic carbonyl compounds, conducting polymers, and imine compounds. The advantages, challenges, and ongoing developments in this area are examined and the potential of organic cathode materials to achieve higher energy density, improved cycling stability, and environmental sustainability is highlighted. The comprehensive analysis of organic cathode materials provides insights into their electrochemical performance, electrode reaction mechanisms, and design strategies such as molecular structure modification, hybridization with inorganic components, porous architectures, conductive additives, electrolyte optimization, binder selection, and electrode architecture to improve their efficiency and performance. In addition, future research in the field of organic cathode materials should focus on addressing current limitations such as low energy density, cycling stability, poor discharge capability, potential safety concerns and improving their performance. To do this, it will be necessary to improve structural stability, conductivity, cycle life, and capacity fading, explore new redox-active organic compounds, and pave the way for the next generation of high-performance energy storage devices. For organic cathode materials to be commercially viable, it is also essential to develop scalable and economical manufacturing processes.

High-throughput protein binder discovery by rapid in vivo selection.

Proteins that selectively bind to a target of interest are foundational components of research pipelines1,2, diagnostics3, and therapeutics4. Current immunization-based5,6, display-based7-14, and computational approaches15-1718 for discovering binders are laborious and time-consuming - taking months or more, suffer from high false positives - necessitating extensive secondary screening, and have a high failure rate, especially for disordered proteins and other challenging target classes. Here we establish Phage-Assisted Non-Continuous Selection of Protein Binders (PANCS-binders), an in vivo selection platform that links the life cycle of M13 phage to target protein binding though customized proximity-dependent split RNA polymerase biosensors, allowing for complete and comprehensive high-throughput screening of billion-plus member protein variant libraries with high signal-to-noise. We showcase the utility of PANCS-Binders by screening multiple protein libraries each against a panel of 95 separate therapeutically relevant targets, thereby individually assessing over 1011 protein-protein interaction pairs, completed in two days. These selections yielded large, high-quality datasets and hundreds of novel binders, which we showed can be affinity matured or directly used in mammalian cells to inhibit or degrade targets. PANCS-Binders dramatically accelerates and simplifies the binder discovery process, the democratization of which will help unlock new creative potential in proteome-targeting with engineered binder-based biotechnologies.

Effect of Different Binders on the Power Characteristics for Carbon Fluorides in Lithium Primary Batteries

Abstract This study demonstrates the effect of different binders on the power characteristics of carbon fluorides (CFx) cathode material for power-type lithium primary batteries. Specifically, polymer binders, such as polyacrylic latex (LA133), poly(vinylidene fluoride) (PVDF) and carboxymethyl cellulose (CMC) are utilized in the preparation of CFx composite electrodes. The selection of binders significantly influences the rate performance of Li/CFx batteries. Among the binders tested, the LA133 binder notably reduces the electrode resistance and interface impedance of the batteries compared to PVDF and CMC, resulting in outstanding rate performance at 1C. Additionally, this study discusses the impact of binder chemistry on the overall performance of the batteries.

The quick screening of binding compounds and proteins for drug discovery and pharmacological research

In drug discovery and pharmacological research, early identification of target molecules for compounds with pharmacological effects is crucial. However, this process often requires significant effort and can be rate-limiting, thereby slowing down research progress. This paper introduces a simplified and rapid method for quick screening of binding compounds or proteins. Utilizing Affinity Selection Mass Spectrometry (ASMS), this technique efficiently detects compound-target binding through size-exclusion chromatography and mass spectrometry. ASMS offers high sensitivity and specificity, making it ideal for accurate identification of binding interactions. We have further enhanced ASMS to handle membrane proteins without solubilization, creating Binder Selection Technology (BST). BST allows screening against both soluble and challenging membrane proteins such as GPCRs and SLC transporters. By using cell membrane fractions or organelle fractions with high target molecule expression, BST efficiently identifies potential binding compounds. This innovative method constructs a comprehensive database of binding compounds for various targets, facilitating rapid hypothesis testing and pharmacological evaluation. Additionally, BST screens 17,000 proteins, including membrane proteins, using wheat germ cell-free and animal cell expression systems. This approach allows exploration of binding interactions without labeling compounds or immobilizing proteins, preserving their native state. BST is powerful for identifying targets of compounds with known pharmacological effects but unknown targets in animal or cell-based assays. By utilizing BST, researchers can overcome bottlenecks in early drug discovery, significantly enhancing research speed and success rates. This method represents a major advancement, providing an efficient and effective way to identify and validate target molecules in drug discovery.

A platform for the early selection of non-competitive antibody-fragments from yeast surface display libraries.

In this work, we report the development of a platform for the early selection of non-competitive antibody-fragments against cell surface receptors that do not compete for binding of their natural ligand. For the isolation of such subtype of blocking antibody-fragments, we applied special fluorescence-activated cell sorting strategies for antibody fragments isolation from yeast surface display libraries. Given that most of the monoclonal antibodies approved on the market are blocking ligand-receptor interactions often leading to resistance and/or side effects, targeting allosteric sites represents a promising mechanism of action to open new avenues for treatment. To directly identify these antibody-fragments during library screening, we employed immune libraries targeting the epidermal growth factor receptor as proof of concept. Incorporating a labeled orthosteric ligand during library sorting enables the early selection of non-competitive binders and introduces an additional criterion to refine the selection of candidates exhibiting noteworthy properties. Furthermore, after sequencing, more candidates were identified compared to classical sorting based solely on target binding. Hence, this platform can significantly improve the drug discovery process by the early selection of more candidates with desired properties.

Impact of Binder Selection on Functional Properties of Polymer Nanocomposite Featured with Metal Oxide Nanoparticle

The effectiveness of nanocomposite materials depends on the accuracy of the binder selection process. This process is crucial for ensuring compatibility, better adhesive behaviour, and stability during the synthesis of polymer composites with metal nanoparticles. An investigation was conducted to analyze the accuracy and efficiency of binder materials on metal nanoparticle (oxide) featured polymer composites. The investigation utilized Advanced Spectroscopic Computational Optimization Analysis (ASCOA) and high-throughput experimental methods to identify and optimize binders using computational modelling (ACM). The processes driving binder-nanoparticle interactions were unravelled by combining advanced characterization methods such as Transition Metal Oxide-based Materials (TMO-M), non-hydrolyzable sialic acid (N-HSIA), and oxygen reduction reaction process (ORR) investigations. In-depth simulation analyses were performed to verify the effectiveness of the proposed methods and gain further understanding. These simulations investigated alternative binding arrangements to maximize material performance while considering sustainability and economic factors. The results demonstrated how binder choice affects material properties, which can be valuable for designing better nanocomposite materials for specific purposes. Additionally, the ASCOA and ACM analyses revealed an accuracy ratio of more than 90% and efficiency ratios of 86% and 84% for ASCOA and ACM, respectively.

Proximity-driven site-specific cyclization of phage-displayed peptides

Cyclization provides a general strategy for improving the proteolytic stability, cell membrane permeability and target binding affinity of peptides. Insertion of a stable, non-reducible linker into a disulphide bond is a commonly used approach for cyclizing phage-displayed peptides. However, among the vast collection of cysteine reactive linkers available, few provide the selectivity required to target specific cysteine residues within the peptide in the phage display system, whilst sparing those on the phage capsid. Here, we report the development of a cyclopropenone-based proximity-driven chemical linker that can efficiently cyclize synthetic peptides and peptides fused to a phage-coat protein, and cyclize phage-displayed peptides in a site-specific manner, with no disruption to phage infectivity. Our cyclization strategy enables the construction of stable, highly diverse phage display libraries. These libraries can be used for the selection of high-affinity cyclic peptide binders, as exemplified through model selections on streptavidin and the therapeutic target αvβ3.

Generation of Chicken Antibody Libraries and Selection of Antigen Binders.

Chicken antibodies have been widely used for research and diagnostic purposes. Chicken antibodies are often cross-reactive to epitopes shared by humans, nonhuman primates, and other mammals, and can be tested in many mouse disease models, which provides an advantage for their preclinical study and evaluation. In addition, the variable region of chicken antibodies has unique structural characteristics, including noncanonical cysteine residues in the heavy chain complementarity-determining region (CDR)3 and a long heavy chain CDR3, which together with a short light chain CDR enable the formation of unconventional antibody paratopes. As chickens have single functional copies of the V H and J H genes, and the somatic gene conversion process usually involves D H genes, all functional VDJ gene fragments can be obtained from the B-cell repertoire using a single PCR primer set, without any primer bias. As for the light chain, chickens only have a V λ light chain, composed of a single V λ and J λ gene pair. Therefore, the chicken light chain repertoire can also be accurately amplified using a single primer set. This unbiased reconstitution of the chicken B-cell repertoire provides a great advantage not only in the construction of phage display libraries but also for the in silico selection of antigen binders from a virtual B-cell receptor repertoire. Here, we introduce the use of chicken antibodies in research, diagnostic, and therapeutic fields. In addition, the chromosomal organization of chicken immunoglobulin genes and its diversification mechanisms for shaping the antibody repertoire are also discussed.

Selection of Antigen Binders from a Chicken Single-Chain Variable Fragment Library.

Antibody production against an antigen of interest is highly efficient in chickens, and the use of chicken antibody libraries in phage display can result in high-affinity single-chain variable fragments (scFvs) for multiple applications. After library preparation from an animal immunized with the antigen of interest, the next step involves the identification of antigen binders. Here, we describe a process for the screening of a phage display chicken library using a technique called bio-panning. It consists of several rounds of binding scFv-displaying phage to antigens, followed by washing, elution, and reamplification. We also describe the steps for assessing clone pools obtained after bio-panning via an ELISA-based procedure known as "phage ELISA" to identify single clones. Last, we provide the steps for using high-throughput sequencing to analyze the pool of selected clones.

Impact of Binder Thin-Films on Surface Chemistry of Silicon Anodes in Lithium-Ion Batteries

The effect of polymer binder on the nature and location of solid-electrolyte interphase (SEI) formation on Si active material was investigated. Thin layers of polymeric binder (polyvinylidene fluoride and sodium carboxymethyl cellulose) were spin-coated onto polished single crystal Si wafers. The samples were cycled against a Li counter/reference electrode under various electrochemical conditions in a coin cell configuration. The electrolyte was 1 M of LiPF6 in 1:1:1 wt% EC:DEC:DMC. After cycling, the samples were extracted from the coin cell under inert conditions and X-ray photoelectron spectroscopy (XPS) was performed. Electron microscopy and atomic force microscopy indicate that the binder films are smooth and continuous across the wafer surface, and no impact on the electrochemical behavior was observed. However, notable differences were detected using XPS, which revealed both difference in SEI composition and location relative to the binder-electrolyte and binder-substrate interfaces. These observations and insights will be useful in cell designs, binder selection, and reliability estimates because the location of SEI formation may influence cyclic performance of electrodes.

Development of superpave asphalt binder specifications to meet climate conditions in the UAE

ABSTRACT Asphalt binder's performance is highly sensitive to temperature fluctuations and climatic conditions. The selection of an inappropriate asphalt binder leads to considerable damage and impacts roads' longevity. The current selection practice of asphalt binder in the United Arab Emirates (UAE) is mainly according to the penetration grading system, which does not consider local temperature conditions. The Superpave Performance Grade (PG) system considers extreme pavement temperatures to define appropriate asphalt binder PG. This study aimed at developing the Superpave asphalt binder PG map for the UAE. The Strategic Highway Research Program (SHRP) and Long-Term Pavement Performance Program (LTPP) Superpave models were used to calculate the pavement temperatures employing air temperature records collected from 20 weather stations across the UAE. The result of the Superpave PG map highlights three distinct asphalt binder grades at 98% reliability: PG 76-10, PG 70-10, and PG 64-10. The PG 76 -10 asphalt binder is the most prevalent PG, covering more than 85% of the UAE map. However, the current construction practice utilizes penetration grades 40/50 and 60/70, through both asphalt binders are equivalent to PG 64-xx. This necessitates the use of different modifier technologies to achieve the Superpave requirements of PG 76-10 and PG 70-10.

Phage Display Panning on Silica: Optimization of Elution Conditions for Selection of Strong Binders.

Phage display panning is a powerful tool to select strong peptide binders to a given target, and when applied to inorganic materials (e.g., silica) as a target, it provides information on binding events and molecular recognition at the peptide-mineral interface. The panning process has limitations with the phage chemical elution being affected by bias toward positively charged binders, resulting in the potential loss of information on binder diversity; the presence of fast growing phages with an intrinsic growth advantage; and the presence of false positives from target unrelated peptides. To overcome some of these limitations, we developed a panning approach based on the sequential use of different eluents (Gly-HCl, pH-2.2; MgCl2, pH-6.1; and TEA, pH-11.0), or pH conditions (Gly-HCl 2.2 < pH < 11.0) that allows the identification of a diverse and comprehensive pool of strong binders. We have assessed and tested the authenticity of the identified silica binders via a complementary experimental (in vivo phage recovery rates and TEM imaging) and bioinformatics approach. We provide experimental evidence of the nonspecificity of the Gly-HCl eluent as typically used. Using a fluorimetric assay, we investigate in vitro binding of two peptides that differ by pI-S4 (HYIDFRW, pI 7.80) and S5 (YSLKQYQ, pI 9.44)─modified at the C terminal with an amide group to simulate net charges in the phage display system, confirming the vital role of electrostatic interactions as driving binding forces in the phage panning process. The presented optimized phage panning approach provides an opportunity to match known surface interactions at play with suitable elution conditions; to select only sequences relevant to a particular interfacial system. The approach has the potential to open up avenues to design interfacial systems to advance our understanding of peptide-assisted mineral growth, among other possibilities.

Evaluation of Polyvinyl Alcohol as Binder during Continuous Twin Screw Wet Granulation.

Binder selection is a crucial step in continuous twin-screw wet granulation (TSWG), as the material experiences a much shorter residence time (2-40 s) in the granulator barrel compared to batch-wise granulation processes. Polyvinyl alcohol (PVA) 4-88 was identified as an effective binder during TSWG, but the potential of other PVA grades-differing in polymerization and hydrolysis degree-has not yet been studied. Therefore, the aim of the current study was to evaluate the potential of different PVA grades as a binder during TSWG. The breakage and drying behavior during the fluidized bed drying of drug-loaded granules containing the PVA grades was also studied. Three PVA grades (4-88, 18-88, and 40-88) were characterized and their attributes were compared to previously investigated binders by Vandevivere et al. through principal component analysis. Three binder clusters could be distinguished according to their attributes, whereby each cluster contained a PVA grade and a previously investigated binder. PVA 4-88 was the most effective binder of the PVA grades for both a good water-soluble and water-insoluble formulation. This could be attributed to its high total surface energy, low viscosity, good wettability of hydrophilic and hydrophobic surfaces, and good wettability by water of the binder. Compared to the previously investigated binders, all PVA grades were more effective in the water-insoluble formulation, as they yielded strong granules (friability below 30%) at lower L/S-ratios. This was linked to the high dispersive surface energy of the high-energy sites on the surface of PVA grades and their low surface tension. During fluidized bed drying, PVA grades proved suitable binders, as the acetaminophen (APAP) granules were dried within a short time due to the low L/S-ratio, at which high-quality granules could be produced. In addition, no attrition occurred, and strong tablets were obtained. Based on this study, PVA could be the preferred binder during twin screw granulation due to its high binder effectiveness at a low L/S-ratio, allowing efficient downstream processing. However, process robustness must be controlled by the included excipients, as PVA grades are operating in a narrow L/S-ratio range.

Wet‐Processable Binder in Composite Cathode for High Energy Density All‐Solid‐State Lithium Batteries

AbstractSulfide‐based all‐solid‐state lithium batteries (ASSLBs) are potential alternatives to conventional lithium‐ion batteries for enhancing energy density and battery safety. However, the industrial sector encounters technical challenges in the fabrication of high‐mass‐loaded composite cathodes to improve the energy densities of ASSLBs. Thus, the selection of an appropriate binder and cathode active material is very important for achieving a good cycling performance of ASSLBs. In this study, wet‐processable poly(ethylene‐co‐methyl acrylate‐co‐glycidyl methacrylate) (EMG) binder and full‐concentration gradient (FCG) LiNi0.78Co0.10Mn0.12O2 (NCM) cathode active material are employed to fabricate the composite cathode with high active mass loading (21.4 mg cm−2). The EMG binder provided strong binding properties to the cathode constituents and improved the electrical conductivity of the composite cathode. The FCG NCM mitigated the morphology damages caused by volume changes in the cathode active material during cycling. Consequently, the solid‐state lithium battery with the composite cathode employing EMG binder and FCG NCM delivered a high discharge capacity of 196.6 mAh g−1 corresponding to an areal capacity of 4.21 mAh cm−2 and showed good capacity retention of 85.1% after 300 cycles at 0.2 C rate and 30 °C.

Exploring Oat Husks as Aggregates in Limestone-Based Composites: Effects of Surface Treatments and Binder Selection on Mechanical Performance.

The viability of incorporating agricultural by-products, such as oat husks, not yet explored in limestone-based composites, as more sustainable alternatives for use as novel aggregates may be improved through the adoption of well-known valorisation strategies applied to other plant-based resources. In this context, this work innovates by assessing how treatments on oat husk surfaces and the choice of limestone-based binders impact the mechanical performance of composites. The strategy adopted to achieve these objectives, in addition to carrying out the physical and geometric characterisation of the husks, consists of treating the husks' surface using washing cycles in water, cement/pozzolan binder, and linseed oil. Furthermore, matrices combining cement, calcium hydroxide Ca(OH)2, and microsilica (SiO2) were used. In conclusion, even though the effects of different binder combinations are inconsistent, coating oat husks-especially with linseed oil-works well in delaying particle degradation and improving mechanical strength compared to untreated particles. Furthermore, when aggregates are substituted with the longer and lamellar particles of oat husk, the impact of the water/cement ratio on mechanical performance and composite workability significantly decreases.

Preparation and Evaluation of Metronidazole Tablets Produced with Different Binders Using Wet Granulation Method

In tablet formulation, binders are essential for ensuring proper powder mix, granulation and overall tablet quality. Variations in binder quality and concentration can impact drug bioavailability, strength and manufacturing processes. The inconsistency in bioavailability and therapeutic response of metronidazole from different manufacturers highlights the importance of binder selection in tablet formulation. This study evaluates the impact of different binding agents on tablet quality. The optimum binder concentration for each of the binders was assessed to obtain suitable concentration that was used to prepare metronidazole tablets. Metronidazole tablets were formulated with four different binder vis, acacia, gelatine, PVP, maize starch at 3% concentration using wet granulation method after which the tablet properties were evaluated. Metronidazole powder exhibited poor flow indices, as indicated by angle of repose: 39.92 ± 1.85, Carr’s compressibility index (CI): 20.13 ± 0.28 and Hausner’s ratio (Hr): 1.26 ± 0.01, whereas its granules exhibited good flow properties. The crushing strength (CS), friability (FR), disintegration time (DT) (CSFR/DT) ratio for batches showed values in 3% binder concentration, indicating higher strength as compared to other concentrations. There was a significant increase (P &lt; 0.05) in the CSFR/DT ratio for gelatine (2.22) in formulation F2 compared to maize starch in Formulation F4. The formulated tablets with the various binders have met with the British Pharmacopeial criteria of 80% drug release from uncoated immediate-release tablets. Amongst the four binders, gelatine was found to be the best in the formulation of robust metronidazole tablets by wet granulation method at an optimised concentration of 3% w/w. Tablets produced with gelatin exhibited greater mechanical strength than those produced with other binders, while also demonstrating a slightly longer DT. Metronidazole tablets produced with gelatine have met the British Pharmacopeial requirements including an acceptable in-vitro drug release profile.

Functionalized Binders Boost High‐Capacity Anode Materials

AbstractThe burgeoning field of energy storage battery innovation has sparked a relentless pursuit of high‐capacity anode materials to meet the escalating demand for improved energy density. Typically, these materials for batteries experience significant volume changes during cycles, which severely test the structural integrity and lifespan of electrode configurations. High‐performance binders have emerged as a critical component in addressing this challenge. Although they represent a small proportion of the battery's composition, binders play a pivotal role in enhancing electrochemical efficiency, safety, and cost‐effectiveness of batteries. The advancement of high‐capacity anode materials has rendered traditional binders inadequate, prompting the development of functional binders that are increasingly being refined to meet these requirements. This article began by outlining the role and requirements of binders within electrodes, examining cutting‐edge characterization methodologies, and discussing the “structure‐function” paradigm that underpins binder selection. It then showcased the research advancements in identifying suitable binders for high‐capacity anode materials, including silicon (Si), phosphorus (P), tin (Sn), antimony (Sb), and germanium (Ge). In summary, the article contemplated the future direction of binder development and application in high‐capacity electrode materials. The aim is to facilitate the progression of high‐performance, high‐capacity anodes, thereby accelerating the development of high‐energy‐density lithium‐ion and sodium‐ion batteries.

Study of binder effect on the lithium storage kinetics of copper phosphide nanotube anode

Study of binder effect on the lithium storage kinetics of copper phosphide nanotube anode