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The American Society of Addiction Medicine (ASAM) Criteria Validity Study at Massachusetts General Hospital and Harvard Medical School randomized patients between programs in two levels of care. It therefore became critical to determine the extent to which programs met ASAM level of care (LOC) descriptions. Quantitative surveys (checklist) and qualitative case studies (field observation, key informant interviews) documented care variation within and between two ASAM LOCs in 12 substance abuse treatment units. These LOCs were: Level II (Intensive Outpatient Treatment) and Level III (Medically Monitored Residential Treatment). The Level II and Level III programs, as a group, met ASAM LOC criteria, but data showed major within-level variation by hours per day and number and type of skilled treatment services. Observational data suggest considerable within-level variation due to managed care and staff training. In multi-site PPC validity studies, it will be crucial to examine within-LOC variation and take into account payment sources and staff training when assessing patient outcomes. [ABSTRACT FROM AUTHOR]

Harnessing the unique optical properties of chirality-enriched single-walled carbon nanotubes (SWCNTs) is the key to unlocking the application of SWCNTs in photonics. Recently, it has been discovered that chemical modification of SWCNTs greatly increases their potential in this context. Despite the dynamic progress in this area, the mechanism of the chemical modification of SWCNTs and the impact of the reaction conditions on the properties of the obtained functional nanomaterials remain unclear. In this study, we demonstrate how the reaction environment influences the observed fluorescence pattern of SWCNTs after modification with benzoyloxy radicals generated in situ . The obtained results reveal that each diacyl peroxide molecule can generate either one or two radicals by two different mechanisms, i.e. , induced or spontaneous decomposition. Through proper selection of the reactant concentration, process temperature, and solvent, we were able to activate one or both radical decay pathways. In addition, the choice of a solvent, such as tetrahydrofuran or acetonitrile, allowed drastic changes in the functionalization process. Consequently, the SWCNT surface was grafted with functional groups via C-C bonds using radicals derived from the solvent molecules instead of attaching an aromatic moiety from the reactant present in the system through the expected C-O linkage. Verification of the structure of the chemically bound functional groups through hydrolysis opens the route to further modification of SWCNT surfaces using the labile ester connection. By gaining a better understanding of the emergence and behavior of the generated radicals, we demonstrate the possibility of controlling the density of introduced defects, as well as the selectivity of the functionalization process. The identification of the underlying chemical pathways responsible for the functionalization of SWCNTs paves the way for the design of precise methods of SWCNT modification to adjust their photonic characteristics for specific applications., Competing Interests: There are no conflicts of interest to declare., (This journal is © The Royal Society of Chemistry.)

Single-walled carbon nanotubes (SWCNTs) are synthesized as mixtures of various SWCNT types, exhibiting drastically different properties, and thereby making the material of limited use. Fluorene-based polymers are successful agents for purifying such blends by means of conjugated polymer extraction (CPE), greatly increasing their application potential. However, a limited number of studies have devoted attention to understanding the effects of the polyfluorene backbone and side chain structure on the selectivity and separation efficiency of SWCNTs. Regarding the impact of the polymer backbone, it was noted that the ability to extract SWCNTs with conjugated polymers could be significantly enhanced by using fluorene-based copolymers that exhibit dramatically different interactions with SWCNTs depending on the types of monomers combined. However, the role of monomer side chains remains much less explored, and the knowledge generated so far is fragmentary. Herein, we present a new approach to tailor polymer selectivity by creating copolymers of polyfluorene bearing mixed-length alkyl chains. Their thorough and systematic analysis by experiments and modeling revealed considerable insight into the impact of the attached functional groups on the capacity of conjugated polymers for the purification of SWCNTs. Interestingly, the obtained results contradict the generally accepted conclusion that polyfluorene-based polymers and copolymers with longer chains always prefer SWCNTs of larger diameters. Besides that, we report that the capacity of such polymers for sorting SWCNTs may be substantially enhanced using specific low molecular weight compounds. The carried-out research provides considerable insight into the behavior of polymers and carbon-based materials at the nanoscale.

One of the ways to turn concrete into smart concrete involves the incorporation of conductive fillers. These fillers should be evenly distributed in the matrix to enable the charge propagation necessary for sensing. To homogenize the mixture, typical surface-active chemical compounds are routinely employed. Unfortunately, their presence often negatively impacts the characteristics of concrete. In this work, we show that conductive multi-walled carbon nanotubes (MWCNTs) can be included in the concrete matrix by using off-the-shelf lignosulfonate-based plasticizers. These plasticizers showed a much-improved capability to disperse MWCNTs compared to other routinely used surfactants. They also prevented a significant deterioration of the consistency of the mixture and inhibited the acceleration of the hydration process by MWCNTs. In concretes with MWCNTs and lignosulfonate-based plasticizers, the mechanical properties were largely preserved, while the nanocomposite became electrically conductive. Consequently, it enabled evaluation of the condition of the material by electrical impedance measurements.

Carbon-based nanomaterials have catalyzed breakthroughs across various scientific and engineering disciplines. The key to unlocking a new generation of tailor-made nanomaterials based on single-walled carbon nanotubes (SWCNTs) lies in the precise sorting of raw material into individual chiralities, each possessing unique properties. This can be achieved using conjugated polymer extraction (CPE), but to a very limited extent since the process generates only a few chirality-enriched suspensions. Therefore, it is imperative to comprehend the mechanism of the wrapping of SWCNTs by polymers to unleash CPE's full potential. However, the lack of a diverse palette of chirality-selective polymers with varying macromolecular parameters has hindered a comprehensive understanding of how the nature of the polymer affects the performance and selectivity of SWCNT isolation. To address this gap, multiple batches of such polymers are synthesized to elucidate the impact of molecular weight and dispersity on the purity and concentrations of the generated SWCNT suspensions. The obtained results explain the inconsistent outcomes reported in the literature, greatly improving the application potential of this promising SWCNT sorting approach. Concomitantly, the discovered significant influence of the macromolecular characteristics of conjugated polymers on the SWCNT isolation efficacy sheds considerable insight into the unresolved mechanism of this sorting technique., (© 2024 The Author(s). Advanced Science published by Wiley‐VCH GmbH.)

Transforming amines with low boiling points and high volatilities into protic salts is a versatile strategy to utilize low molecular weight compounds as precursors for N-doped carbon structures in a straightforward carbonization procedure. Herein, conventional mineral acids commonly used for the synthesis of protic salts were replaced by bio-derived phytic acid, which, combined with various amines and amino acids, yielded partially or fully bio-derived protic salts. The biomass-based salts showed higher char-forming ability than their mineral acid-based analogs (up to 55.9% at 800°), simultaneously providing carbon materials with significant porosity (up to 1177 m 2 g -1 ) and a considerable level of N,P,O-doping. Here, we present the first comprehensive study on the correlation between the structure of the bio-derived protic precursors and the properties of derived carbon materials to guide future designs of biomass-derived precursors for the one-step synthesis of sustainable carbon materials. Additionally, we demonstrate how to improve the textural properties of the protic-salt-derived carbons (which suffer from high brittleness) by simply upgrading them into highly flexible nanocomposites using high-quality single-walled carbon nanotubes. Consequently, self-standing electrodes for the oxygen reduction reaction were created., (© 2024. The Author(s).)

One-dimensional transition metal materials are promising supports for precious metals used in energy production processes. Due to their electrochemical properties, 3d-group metals (such as Ni, Co, and Fe) can actively interact with catalysts by a strong metal-support interaction. This study shows that changing the Ni:Co ratio makes it possible to modulate the structure of the catalyst supports, which, in turn, provides a tool for designing their electrical and electrochemical properties. For example, Ni 1 -Co 9 shows the highest electrical conductivity (5.8-10 -4 S/cm) among all of the materials examined. On the contrary, the Pd@Ni 7 -Co 3 system presents the highest mass activity (>2000 mA mg -1 ) at 0.7 V, exceeding by several times that of commercial Pt/C (>300 mA mg -1 ) at the same potential. Our study opens the gateway for applications of bimetallic transition metal nanowires in catalytic conversion and energy production processes.

The aim of this article is to experimentally determine the role of the environment, consisting of a base oil (PAO), carbon nanomaterials, and optional other additives, as well as the kind of metal in contact with the lubrication film, in the stimulation of zinc dialkyldithiophosphate (ZDDP) additives' effectiveness during protective film formation. This paper focuses on the role of carbon nanostructures in energy transportation and conversion during tribological processes. An antistatic additive (ASA) (not used in lubricating oils) for jet fuels was added to disturb the process of energy conduction (electric charges) through the lubricant film and thus determine how this disturbance affects the kinetics of the ZDDP triboreaction and, consequently, the linear wear. To achieve this research goal, two types of tribological testing devices were used: an Anton Paar tribometer (TRB) and a triboelectric tribometer (TET). The novelty of the present research is in the use of the method for disturbing the flow of charge/energy through the lubricant film with an antistatic additive for jet fuels, ASA, to influence the impact of this energy on the antiwear properties of ZDDP. The following conclusions were drawn: (1) carbon-based nanostructures, i.e., CNTs, AuCNTs, graphene, and fullerenes, are able to change the rate of chemical reactions of ZDDP during tribological processes; (2) CNTs have the ability to catalyze tribochemical reactions of ZDDP, while graphene and fullerenes are not able to perform this effectively; (3) AuCNT takes the role of an inhibitor during ZDDP's triboreaction; and (4) by discharging electric charge/energy, ASA, in cooperation with CNT and AuCNT significantly reduces the rate of the ZDDP reaction.

Conjugated polymers are promising tools to differentiate various types of semiconducting single-walled carbon nanotubes (s-SWCNTs). However, their synthesis is challenging. Insufficient control over molecular weights, and unpredictive/unrepeatable batches hinder possible applications and scale-up. Furthermore, commercial homogeneous catalysts often require inert conditions and are almost impossible to recycle. To overcome these problems, we present a nanocatalyst consisting of magnetic nickel nanowires decorated with highly active palladium nanoparticles. A two-step wet chemical reduction protocol with the assistance of sonochemistry was employed to obtain a heterogeneous catalyst capable of conducting step-growth Suzuki polycondensation of a fluorene-based monomer. Additionally, we enhanced the performance of our catalytic system via controlled microwave irradiation, which significantly shortened the reaction time from 3 d to only 1 h. We studied the influence of the main process parameters on the yield and polymer chain length to gain insight into phenomena occurring in the presence of metallic species under microwave irradiation. Finally, the produced polymers were used to extract specific s-SWCNTs by conjugated polymer extraction to validate their utility., (© 2024. The Author(s).)

The inability to purify nanomaterials such as single-walled carbon nanotubes (SWCNTs) to the desired extent hampers the progress in nanoscience. Various SWCNT types can be purified by extraction, but it is challenging to establish conditions giving rise to the isolation of high-purity fractions. The problem stems from the fact that common organic solvents or water cannot provide an optimal environment for purification. Consequently, one must often decide between the separation yield and purity of the product. This article reports how through the self-synthesis of poly(9,9-dioctylfluorene-alt-benzothiadiazole) with tailored characteristics, in-depth elucidation of the extraction process, and mixed-solvent engineering, a high-yield isolation of monochiral (7,3) SWCNTs is developed. The combination of toluene and tetralin affords a separation medium of unique properties, wherein both high yield and exceptional purity can be attained simultaneously. The reported results pave the way for further research on this rare chirality, which, as illustrated herein, is much more reactive than any of the previously separated SWCNTs., (© 2023 The Authors. Small published by Wiley-VCH GmbH.)

Despite the extensive utilization of carbon nanostructures as sensors, the factors that most affect their performance remain insufficiently understood. Many nanocarbon-based sensors are either processed in liquid environments or applied as liquid suspensions, which leads to solvatochromism, substantially influencing the underlying optical transitions. Most of the principles established so far apply only to nanocarbon species dispersed in polar environments by common surfactants, so the reported findings are not universal. For instance, they cannot describe the behavior of single-walled carbon nanotubes (SWCNTs) suspended in organic solvents by conjugated polymers (CPs), which have recently received considerable attention from the scientific community. Our research responds to this lack of knowledge and provides a thorough understanding of this topic by investigating SWCNT nanocomposites based on polyfluorenes and their co-polymers. A careful selection of an autonomous reference and precise spectral analysis allowed us to measure absolute solvatochromic shifts, by using which we identified and derived the underlying relationships affecting the optical properties of the material. Elucidation of the complex interactions between the polymer structure, SWCNT chirality, and solvent characteristics gave rise to the formulation of a revised mechanism of solvatochromism in SWCNTs. The in-depth experimental and theoretical examination revealed that in the case of CP-solubilized SWCNTs, the solvatochromic shifts strictly depend on the assignment of individual chiral types to mods and families, which experience the strain exerted by the polymer chains in different ways.

In this work, a Pluronic/Dextran system was developed to discover the mechanism of the aqueous two-phase extraction (ATPE) technique, which is widely employed for the sorting of single-walled carbon nanotubes (SWCNTs) and other types of nanomaterials. The role of the phase-forming components and partitioning modulators was comprehensively investigated to gain greater insights into the differentiation process. The obtained results revealed that sodium dodecyl sulfate and sodium dodecylbenzene sulfonate operated as excellent partitioning modulators, enabling the diameter-based sorting of SWCNTs. Additionally, the data strongly suggested that different densities of various SWCNT species drove the movement of SWCNTs in the ATPE system. Consequently, the largest diameter SWCNTs were first influenced by surfactants and, thus, the nanotubes migrated towards a lower density top phase in the following order (7,5) > (8,3) > (6,5) > (6,4). Based on the in-depth analysis of the partitioning system, a mechanism was proposed that described the method in which the popular ATPE separation technique operates.

Monochiral single-walled carbon nanotubes (SWCNTs) are indispensable for advancing the technology readiness level of nanocarbon-based concepts. In recent times, many separation techniques have been developed to obtain specific SWCNTs from raw unsorted materials to catalyze the development in this area. This work presents how the aqueous two-phase extraction (ATPE) method can be enhanced for the straightforward isolation of (6,4) SWCNTs in one step. Introducing nonionic surfactant into the typically employed mixture of anionic surfactants, which drive the partitioning, is essential to increasing the ATPE system's resolution. A thorough analysis of the parameter space by experiments and modeling reveals the underlying interactions between SWCNTs, surfactants, and phase-forming agents, which drive the partitioning. Based on new insight gained on this front, a separation mechanism is proposed. Notably, the developed method is highly robust, which is proven by isolating (6,4) SWCNTs from several raw SWCNT materials, including SWCNT waste generated over the years in the laboratory., (© 2023 The Authors. Advanced Science published by Wiley-VCH GmbH.)

Silver nanoparticles (AgNPs) have several uses. Many scientists are working on producing AgNPs from plant extracts for use as biomedicines against drug-resistant bacteria and malignant cell lines. In the current study, plant-based AgNPs were synthesized using Raphanus sativus L. (RS) leaf aqua extract. Different concentrations of AgNO 3 were used to optimize the synthesis process of RS-AgNPs from the aqueous leaf extract. Energy-dispersive X-ray analysis (EDX), transmission electron microscopy (TEM), scanning electron microscopy (SEM), atomic force microscope (AFM), and UV-vis spectroscopy were used to analyze the generated materials. Furthermore, to evaluate the biological properties of the obtained materials, Bacillus subtilis (B. subtilis), Pseudomonas aeruginosa (P. aeruginosa), Staphylococcus aureus (S. aureus), Escherichia coli (E. coli), and Candida albicans (C. albicans) pathogen strains were used for the minimum inhibitory concentration (MIC) assays. Subsequently, healthy cell lines (human dermal fibroblast (HDF)) and cancerous cell lines (glioma/U118, Ovarian/Skov-3, and colorectal adenocarcinoma/CaCo-2) were engaged to determine the cytotoxic effects of the synthesized NPs. The cytotoxic and anti-pathogenic potential of AgNPs synthesized by the proposed green approach was investigated. The results were encouraging compared to the standards and other controls. Plant-based AgNPs were found to be potential therapeutic agents against the human colon cancer cell (CaCo-2) and showed strong inhibitory activity on Candida albicans and Staphylococcus aureus growth. The RS-AgNPs generated have highly effective antimicrobial properties against pathogenic bacteria. Our findings also show that green RS-AgNPs are more cytotoxic against cancerous cell lines than normal cell lines. Synthesized nanoparticles with desirable morphology and ease of preparation are thought to be promising materials for antimicrobial, cytotoxic, and catalytic applications., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Nanomaterials have been extensively studied in cancer therapy as vectors that may improve drug delivery. Such vectors not only bring numerous advantages such as stability, biocompatibility, and cellular uptake but have also been shown to overcome some cancer-related resistances. Nanocarrier can deliver the drug more precisely to the specific organ while improving its pharmacokinetics, thereby avoiding secondary adverse effects on the not target tissue. Between these nanovectors, diverse material types can be discerned, such as liposomes, dendrimers, carbon nanostructures, nanoparticles, nanowires, etc., each of which offers different opportunities for cancer therapy. In this review, a broad spectrum of nanovectors is analyzed for application in multimodal cancer therapy and diagnostics in terms of mode of action and pharmacokinetics. Advantages and inconveniences of promising nanovectors, including gold nanostructures, SPIONs, semiconducting quantum dots, various nanostructures, phospholipid-based liposomes, dendrimers, polymeric micelles, extracellular and exome vesicles are summarized. The article is concluded with a future outlook on this promising field., Competing Interests: Competing Interests: The authors have declared that no competing interest exists., (© The author(s).)

Articular cartilage has a low self-repair capacity due to the lack of vessels and nerves. In recent times, nanofiber scaffolds have been widely used for this purpose. The optimum nanofiber scaffold should stimulate new tissue's growth and mimic the articular cartilage nature. Furthermore, the characteristics of the scaffold should match those of the cellular matrix components of the native tissue to best merge with the target tissue. Therefore, selective modification of prefabricated scaffolds based on the structure of the repaired tissues is commonly conducted to promote restoring the tissue. A thorough analysis is required to find out the architectural features of scaffolds that are essential to make the treatment successful. The current review aims to target this challenge. The article highlights different optimization approaches of nanofibrous scaffolds for improved cartilage tissue engineering. In this context, the influence of the architecture of nanoscaffolds on performance is discussed in detail. Finally, based on the gathered information, a future outlook is provided to catalyze development in this promising field., Competing Interests: Competing Interests: The authors have declared that no competing interest exists., (© The author(s).)

Excited-State Intramolecular Photon Transfer (ESIPT) is known for the geometry-related phenolic and imine groups. The Schiff bases formed upon condensation of salicyl aldehyde and glycine led to the formation of ESIPT models. A series of alkali metal salicyliden glycinates were analyzed by X-ray diffraction of their monocrystals and spectroscopy measurements. The X-ray analysis revealed varied hydration levels between the salts. They adapted trans geometry on the imine groups and mostly anticlinal conformation with the neighboring atoms, which is different from the other structurally-related compounds in literature. Fluorescence of these compounds was found for the crystalline forms only. Protonation of the imine nitrogen atom and further proton distribution was consistent with the ESIPT theory, which also explained the observed fluorescence with the highest Stokes shift of 10,181 cm -1 and 10.1% of fluorescence quantum yield for the sodium salt.

Azide functionalization produced luminescent sp 2 -type defects on single-walled carbon nanotubes, by which defect photoluminescence appeared in near infrared regions (1116 nm). Changes in exciton properties were induced by localization effects at the defect sites, creating exciton-engineered nanomaterials based on the defect structure design.

Liver and pancreatic tumors are among the third leading causes of cancer-associated death worldwide. In addition to poor prognosis, both cancer types are diagnosed at advanced and metastatic stages without typical prior symptoms. Unfortunately, the existing theranostic approaches are inefficient in cancer diagnosis and treatment. Carbon nanotubes (CNTs) have attracted increasing attention in this context due to their distinct properties, including variable functionalization capability, biocompatibility, and excellent thermodynamic and optical features. As a consequence, they are now regarded as one of the most promising materials for this application. The current review aims to summarize and discuss the role of CNT in pancreatic and liver cancer theranostics. Accordingly, the breakthroughs achieved so far are classified based on the cancer type and analyzed in detail. The most feasible tactics utilizing CNT-based solutions for both cancer diagnosis and treatment are presented from the biomedical point of view. Finally, a future outlook is provided, which anticipates how the R&D community can build on the already developed methodologies and the subsequent biological responses of the pancreatic and liver cancer cells to the directed procedures., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Charge transport properties in single-walled carbon nanotubes (SWCNTs) can be significantly modified through doping, tuning their electrical and thermoelectric properties. In our study, we used more than 40 nitrogen-bearing compounds as dopants and determined their impact on the material's electrical conductivity. The application of nitrogen compounds of diverse structures and electronic configurations enabled us to determine how the dopant nature affects the SWCNTs. The results reveal that the impact of these dopants can often be anticipated by considering their Hammett's constants and p K a values. Furthermore, the empirical observations supported by first-principles calculations indicate that the doping level can be tuned not only by changing the type and the concentration of dopants but also by varying the orientation of nitrogen compounds around SWCNTs.

Uncommon metal oxidation states in porphyrinoid cofactors are responsible for the activity of many enzymes. The F 430 and P450nor co-factors, with their reduced Ni I - and Fe III -containing tetrapyrrolic cores, are prototypical examples of biological systems involved in methane formation and in the reduction of nitric oxide, respectively. Herein, using a comprehensive range of experimental and theoretical methods, we raise evidence that nickel tetraphenyl porphyrins deposited in vacuo on a copper surface are reactive towards nitric oxide disproportionation at room temperature. The interpretation of the measurements is far from being straightforward due to the high reactivity of the different nitrogen oxides species (eventually present in the residual gas background) and of the possible reaction intermediates. The picture is detailed in order to disentangle the challenging complexity of the system, where even a small fraction of contamination can change the scenario., (© 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.)

Carbon nanotubes (CNTs) play a unique role in the area of flexible conductors as they have remarkably high electrical conductivity and bend easily without deformation. Consequently, CNTs are commonly deposited on substrates as conductive tracks/coatings. Halogenated solvents are often employed to facilitate the deposition process because they dry rapidly due to their high volatility. In this work, we report that halogenated solvents can dope CNTs considerably. The study showed that the use of dichloromethane, chloroform, or bromoform for the CNT deposition significantly impacts the chemical potential of the material, thereby modifying its charge transport characteristics. As a consequence, up to four-fold improvement in electrical conductivity is noted due to doping., (© 2022. The Author(s).)

Partial oxidation of nanocarbon materials is one of the most straightforward methods to improve their compatibility with other materials, which widens its application potential. This work studied how the microstructure and properties of high crystallinity single-walled carbon nanotubes (SWCNTs) can be tailored by applying the modified Hummers method. The influence of temperature (0, 18, 40 °C), reaction time (0 min to 7 h), and the amount of KMnO 4 oxidant was monitored. The results showed that depending on the oxidation conditions, the electronic characteristics of the material could be adjusted. After optimizing the parameters, the SWCNTs were much more conductive (1369 ± 84 S/cm with respect to 283 ± 32 S/cm for the untreated material). At the same time, the films made from them exhibited hydrophilic character of the surface (water contact angle changed from 71° to 27°)., (© 2022. The Author(s).)

Carbon nanotubes (CNTs) have a wide range of unique properties, which have kept them at the forefront of research in recent decades. Due to their electrical and thermal characteristics, they are often evaluated as key components of thermogenerators. One can create thermogenerators exclusively from CNTs, without any metal counterpart, by properly selecting dopants to obtain n- and p-doped CNTs. However, the performance of CNT thermogenerators remains insufficient to reach wide commercial implementation. This study shows that molecular doping and the inclusion of ZnO nanowires (NWs) can greatly increase their application potential. Moreover, prototype modules, based on single-walled CNTs (SWCNTs), ZnO NWs, polyethyleneimine, and triazole, reveal notable capabilities for generating electrical energy, while ensuring fully scalable performance. Upon doping and the addition of ZnO nanowires, the electrical conductivity of pure SWCNTs (211 S/cm) was increased by a factor of three. Moreover, the proposed strategy enhanced the Power Factor values from 18.99 (unmodified SWCNTs) to 34.9 and 42.91 µW/m∙K 2 for CNTs triazole and polyethyleneimine + ZnO NWs inclusion, respectively.

Removal of hazardous herbicides from the aqueous solution is critical for overcoming health-related issues across the wider population. In the current work, we have prepared sodium alginate (SAlg), dextrin, and acrylic acid (AA) based cross-linked hydrogels, composed of bentonite incorporated in the biocompatible hydrogel matrix. This hydrogel composite can remove highly toxic herbicide paraquat (PQ). As-synthesised hydrogel (SAlg/dextrin-cl-PAA) and hydrogel composite (SAlg/dextrin-cl-PAA/bentonite) were further analysed by infra-red spectroscopy (FTIR), X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and thermogravimetric analysis (TGA/DSC). For the first time, PQ adsorption onto sodium and dextrin-based hydrogel was also evaluated. The measured highest removal capacities were 76.923 and 90.909 mg g -1 for the SAlg/dextrin-cl-PAA and SAlg/dextrin-cl-PAA/bentonite, respectively. Pseudo-second-order (PSO) and Langmuir isotherm models have shown to be best suited for accurately describing the adsorption mechanism. A thermodynamics study verified that the adsorption of PQ on adsorbents is spontaneous, favourable and exothermic. Moreover, reusability analysis shows that the adsorbents possess good reproducibility even after six successive cycles. The adsorption results demonstrate that the synthesised adsorbents are very efficient for removing herbicides (PQ) from wastewater., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Large-scale sustainable hydrogen production by water electrolysis requires a highly active yet low-cost hydrogen evolution reaction (HER) electrocatalyst. Conductive carbon nanomaterials with high surface areas are promising candidates for this purpose. In this contribution, single-walled carbon nanotubes (SWCNTs) are assembled into free-standing films and directly used as HER electrodes. During the initial 20 h of electrocatalytic performance in galvanostatic conditions, the films undergo activation, which results in a gradual overpotential decrease to the value of 225 mV. Transient physicochemical properties of the films at various activation stages are characterized to reveal the material features responsible for the activity boost. Results indicate that partial oxidation of iron nanoparticles encapsulated in SWCNTs is the major contributor to the activity enhancement. Furthermore, besides high activity, the material, composed of only earth-abundant elements, possesses exceptional performance stability, with no activity loss for 200 h of galvanostatic performance at - 10 mA cm -2 . In conclusion, the work presents the strategy of engineering a highly active HER electrode composed of widely available elements and provides new insights into the origins of electrocatalytic performance of SWCNT-based materials in alkaline HER., (© 2021. The Author(s).)