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Purpose: Core strength is vital for athletic performance, and many more exercises that involve the kinetic chain have been designed for able-bodied athletes. Disabilities that impair the kinetic chain can reduce the effectiveness of strength training. However, the impact of amputation on core strength training of people with disabilities and its underlying mechanism remains unclear. This study aimed to evaluate the muscle activation patterns and levels in athletes with amputation during 4 basic and modified weight-bearing core strength-training exercises. Methods: Fifteen elite athletes with unilateral amputation (170.6 [7.3] cm; 63.9 [11.9] kg; 25.9 [5.3] y) volunteered for this study. Surface electromyography was used to measure the muscle activity mainly in the lumbopelvic–hip complex-stabilizing muscles during 4 kinetic chain trunk exercises with and without modifications. Results: The significance level was set at α =.05. The results showed a significant difference in muscle activation between different body sides (P <.05). Specifically, amputation on the support position resulted in a diagonal pattern of muscle activation, and amputation on the free distal segments resulted in a unilateral dominant pattern with higher activation in muscles on the nonamputated side (P <.05). Modifications led to significant decreases in muscle activation asymmetry index (P <.05). Conclusions: Amputation caused muscle activation asymmetry and 2 activation patterns. Modifications by enhancing proximal stability and adjusting distal loading effectively reduced the asymmetry of muscle activation. Coaches and clinicians can use these results to tailor exercises for athletes with disabilities in training and rehabilitation. [ABSTRACT FROM AUTHOR]

Guinea grass seed starch nanoparticles (GSNPs) Were prepared via nanoprecipitation and dual‐modified with 3% octenyl succinic anhydride (OSA) and pulsed electric fields (PEF) (1.5, 3.0, and 4.5 kV cm⁻¹). Native and modified GSNPs Were assessed for cytotoxicity (Caco‐2 cells), in vitro digestibility, and their ability to stabilize Pickering emulsions. The cytotoxicity results showed no significant impact on cell viability or metabolic activity across all concentrations and modifications. The digestibility profile revealed that native GSNPs Were more digestible (62.61%) compared to modified samples (53.49%). The logarithmic slope analysis indicated that the digestion profiles of all samples followed a linear trend (r² 〉 0.86), characterized by first‐order kinetics. Pickering emulsions containing 0.25–2% GSNPs exhibited good stability, with higher concentrations (1–2%) ensuring 100% emulsified phase coverage and excellent storage stability. Droplet sizes ranged from 171.32 to 536.41 nm, and zeta potentials from −28.68 to −9.87 mV over two months. Microscopy confirmed that all emulsion droplets Were spherical, with smaller droplet sizes observed. The emulsions displayed shear‐thinning flow behavior, where apparent viscosity decreased with increasing shear rate, and increased with modification. These findings suggest that GSNPs have significant potential for use in forming stable Pickering emulsions. [ABSTRACT FROM AUTHOR]

The polyethylene terephthalate (PET) fibers surfaces were modified by complexing tannic acid (TA)-iron ions (Fe3+) to form a metal skeleton structure on the fibers. In this system a large number of phenolic hydroxyl groups, epoxy groups and other active groups on the fibers surfaces can stabilize the metal skeleton structure and enhance the interfacial peeling performance between the fibers and the composite rubber matrix. The modified PET fibers were analyzed by scanning electron microscopy (SEM), thermogravimetric analysis (TGA) and mechanical properties. The results showed that the peeling strength between the modified fibers and the rubber matrix was increased 45%. This method has the advantages of simple operation, mild conditions and low cost, which provides a new idea for the preparation of rubber/polyester fiber composites with excellent mechanical properties. [ABSTRACT FROM AUTHOR]

Fly ash (FA) was used to modify sludge-based biochar (SBC) to improve its phosphorus (P) adsorption capacity, which was conducted by adding FA in the dried sewage sludge before 600 °C pyrolysis. FA modification increased the surface area of SBC, decreased its average pore diameter, increased its Al and Fe contents, improved its crystallinity, and enhanced its maximal P adsorption capacity from 12.37 mg adsorbed P/g SBC (mg/g) to 14.05 mg/g. The P adsorption process was well fitted by the pseudo-second-order kinetic and Langmuir isotherm models, indicating that P adsorption onto SBC was a single molecular layer adsorption dominated by chemical adsorption. The P adsorption onto SBCs was spontaneous and endothermic. FA modification improved the reusability of SBC by increasing the retention rate from 74.9 ± 5.8% to 80.8 ± 5.4% after four adsorption and desorption cycles. FA modification changed the P adsorption mechanism of SBC from ligand exchange, electrostatic attraction, and ion exchange to surface inner-sphere complex formation, electrostatic attraction, and ion exchange. [ABSTRACT FROM AUTHOR]

Photopolymers, which are composed of monomer, oligomer polymer, and their combinations and exhibit photochemical reactions when exposed to light, are now commonly employed in 3D printers, particularly in the flexographic printing industry, and are becoming waste. The utilization of waste solid sheet Photopolymer Plates (PhP) for bitumen modification is an efficient way of disposing of post-consumer items and an alternate method of obtaining new, high-quality modifiers. The consequences of using waste PhP in bitumen modification, both independently and in conjunction with Styrene–Butadiene–Styrene (SBS) were explored. By combining PhP and SBS, it is hoped that savings can be made without sacrificing performance due to the high rate of single SBS modification. The modified binders prepared using PhP and SBS both separately and together were subjected to conventional and rheological tests. The performance of 5% SBS modification could not be achieved at the highest rate that PhP can be used alone without creating a workability problem. The use of 5–7% PhP in combination with 2% SBS outperformed the single 5% SBS modification. This combined binder did not cause workability problems and showed good low and high-temperature behavior and was found to be an economical alternative to SBS modification. [ABSTRACT FROM AUTHOR]

The synthesis of modified mesoporous silica (SBA-15), a powerful and highly effective adsorbent, was provided for the preconcentration, extraction, separation, and determination of trace amounts of Ni (II) ions. In this method, SBA-15 modified with 1-(2-thiazolylazo)-2-naphthol (TAN) was used as a suitable absorbent. The absorption of Ni (II) ions was studied using the FAAS technique. Transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET), energy-dispersive spectroscopy (EDS), Fourier-transform infrared (FT-IR) spectroscopy, and CHNS elemental analysis techniques were used to assess the characteristics of SBA-15 and TAN/SBA-15. Effective parameters (pH, amount of nanocomposite, extraction time, and type of recovery solvent) for extracting Ni (II) ions via TAN/SBA-15 were investigated. The merit figures of the method were obtained with appropriate results, such as detection limit, accuracy, enrichment factor, and preconcentration factor. The calibration curve was linear within the range of 5.0-50 ng mL-1 with a detection limit of 1.8 ng mL-1. High preconcentration, small relative standard deviations, and enrichment factors (approximately 100) were represented by the statistical analysis. The proposed method for measuring Ni (II) ions was used at trace levels in real samples, such as seawater, river water, well water, and wastewater from a textile factory, an electrical power station, an MDF factory, and a food industrial company, with satisfactory results. [ABSTRACT FROM AUTHOR]

Wood modification processes based on citric acid in combination with various copolymers have gained in importance in recent years. These processes also include modification with citric acid (CA) and sorbitol, a sugar alcohol, which is currently in the industrial realisation phase in Germany (SorCA) and Norway (CIOL). The modification of wood with sorbitol and citric acid (SorCA) can significantly improve the dimensional stability and durability of the wood. It is hypothesised that the addition of a copolymer may improve the fixation of the chemicals within as well as the flexibility of the modified wood matrix. In this study, the macroscopic changes, the fixation of the chemicals and the impact bending properties of wood modified with CA and SorCA are compared. Both modifications cause a permanent increase in mass (WPG) and volume (CWB). The fixation of the chemicals was comparable for both modifications; at high chemical concentrations, the SorCA polyester fixed slightly better within the wood matrix. Both modifications led to embrittlement of the wood, measured by a decrease in the impact bending strength (IBS). This embrittlement was clearly concentration-dependent and slightly more pronounced for the modification with CA. [ABSTRACT FROM AUTHOR]

Ceramic membranes are increasingly recognized for their effectiveness in processing fermentation broths. However, developing ceramic membranes with superior anti-fouling properties remains a challenge for large-scale applications. Iron oxide nanomaterials have gained significant research interest as a cost-effective and readily available solution for mitigating membrane fouling, thanks to their excellent hydrophilicity. This study introduces ceramic membranes enhanced with iron oxide via a facile sol-gel technique. The membrane's resistance to fouling, hydrophilicity, adhesion force, and surface potential were assessed. Post-modification, a consistent distribution of iron elements on the membrane surface was achieved, with negligible alteration in pore size. Although the pure water permeance (450 ± 45 L m−2 h−1·bar−1) did not change significantly, the permeance of the modified membrane (225 L m−2 h−1·bar−1) was nearly 20 % higher than that of the original membrane when separating a 1000 ppm oil-in-water emulsion, with both membranes achieving 99 % oil droplet rejection. Moreover, the flux recovery rate of the modified membrane surpassed that of the original membrane by approximately 30 %, indicating a significant improvement in anti-fouling performance. Upscaling experiments further validated the modified membrane's anti-fouling performance and capability to rapidly process broths with high oil content. Overall, this study presents a novel anti-fouling ceramic membrane for the treatment of oil-containing fermentation systems. [ABSTRACT FROM AUTHOR]

Introduction: Elephant foot yam starch is highly susceptible to enzymatic digestion. To address this, heat-moisture treatment (HMT) has been used to modify its digestive properties and functionalities. However, when using modified starch in various food compositions, it is ultimately necessary to cook it in waterrich environments. The present work thus offers a systematic understanding of the heating and cooking procedures for modified starch, with a view to maintaining its structural and digestive properties. Methods: Experimental investigations employing X-ray diffraction, scanning electron microscopy, and enzymatic digestion have been utilized to gain insights into the characteristics of cooked starches. The interactions between amylose and amylopectin in native starch are more susceptible to disruption during cooking, which results in changes in texture and a reduction in resistant starch (RS) retention. Additionally, these preparations have been investigated by tribology to test structure and and friction. Results and discussion: The application of HMT has been observed to induce changes that stabilize the interactions between amylose and amylopectin, thereby ensuring better maintenance of granular integrity and higher RS retention under specific cooking conditions. The findings indicate that following a 2-min cooking period at 100°C, the modified elephant foot yam starch (EFYS) demonstrated enhanced granular stability, which was subsequently compromised after 10 min of cooking. Additionally, when modified elephant foot yam starch (EFYS) was heated at a temperature of 86°C for 2 and 6 min, it demonstrated superior preservation of resistant starch (RS) in comparison to a cooking time of 10 min. Moreover, the HMT starch exhibited the highest RS retention when cooked at 100°C for 2 and 6 min at approximately 39.12% and 20.23%, respectively. However, this retention decreased significantly to 1.08% after 10 min of cooking. Furthermore, the insights from tribology, when combined with the proposed naive models, enhance the understanding of how preparation conditions affect the functionalities of starches, which is crucial for designing food products with desired textural and nutritional qualities, especially in water-rich environments, where maintaining structural integrity and RS content is important. [ABSTRACT FROM AUTHOR]

Introduction: Long working hours are likely associated with the decreased of kidney function, while physical activity (PA) was linked to improvements in kidney function. However, whether PA can offset the negative impact of long working hours on kidney function was unclear, which is the focus of this study. Methods: A cross-sectional study was conducted. Three approaches were adopted to distinguish the association between long working hours and regular working hours. Moderate to vigorous physical activity (PA) was assessed by a structured questionnaire. eGFR and chronic kidney disease (CKD) or not were utilized to evaluate the kidney function. Linear and logistic regression analyses were conducted to assess the association between weekly working hours, PA, and kidney function. Results: A total of 18,431 adults were enrolled in this study, including 9981 males (54.2%) and 8450 females (45.8%). The average eGFR was (99.54 ± 17.55 mL/min/1.73 m2). The people worked more than 40 h/wk (98.89 ± 17.06 mL/min/1.73 m2) had lower eGFR compared to those worked less than 40 h/wk (99.93 ± 17.83 mL/min/1.73 m2) (p < 0.05). Individuals working longer hours exhibited lower eGFR (β = -0.772, 95% CI: -1.241, -0.303, for > 40 h/wk compared to working ≤ 40 h/wk). Engagement in moderate to vigorous PA was associated with higher eGFR values (β = 1.159, 95% CI: 0.699, 1.619) compared to low PA ( < 150 minutes/wk), but this association did not reach statistical significance for the prevalence of CKD. Furthermore, PA was insufficient to reverse the decline of eGFR related to prolonged working hours. Discussion: Prolonged working hours were associated with a decline in eGFR, while PA was found to have a protective effect on kidney function. However, PA alone may not fully mitigate the negative impact of prolonged working hours on renal health. More robust measures to protect renal function should be implemented to mitigate the damage caused by prolonged working hours. [ABSTRACT FROM AUTHOR]

The fungus Pleurotus eryngii (PE) was modified with six different methods. The modified Pleurotus eryngii (MPE) and PE fungi samples were characterized by (Fourier transform infrared) FTIR technique and thermogravimetry to understand the mechanism of modifications. Surface analysis of the fungi samples were compared with scanning electron microscope (SEM), energy dispersive X-ray analysis (EDX), and Brunauer–Emmett–Teller (BET) characterizations. Cetyltrimethylammonium bromide (CTAB) modification enhanced the adsorption capacity of PE for rhodamine B from 12.4 to 19.2 mg.g−1 that is the maximum at pH 8. The adsorption capacity of the CTAB-modified Pleurotus eryngii (CMPE) was reduced to 8.55 mg.g−1, 3.80 mg.g−1, and 5.80 mg.g−1 in aqueous solutions of Na2CO3, NaCl, and NaNO3, respectively, as well as the effect of the aqueous solutions of Pb2+ and Ni2+ on adsorption capacity were limited. The adsorption capacity of the CTAB-modified Pleurotus eryngii for rhodamine B was compared with Aspergillus niger (10.3 mg.g−1). The biosorption of CMPE was relatively high for reactive black 5 (96.0 mg.g−1) and reactive red 120 (98.5 mg.g−1) at about five times for rhodamine B. The adsorption isotherm was fitted well for the Langmuir model for PE and CMPE with a favorable adsorption. The kinetics of the adsorption process was pseudo-second order for PE and CMPE. The decrease of the adsorption capacity was observed for fungi samples with an exothermic adsorption process. [ABSTRACT FROM AUTHOR]

This work explores the conversion of raw poultry manure (RPM) into tailor-made biochars for an efficient phosphorus (P) recovery from aqueous solutions. To this end, three RPM-functionalized biochars with Mg (RPM-B-Mg), Al (RPM-B-Al), and Mg/Al-layered double hydroxides (RPM-B-Mg/Al-LDHs) were synthetized, deeply characterized, and then tested for P recovery under various experimental conditions. Biochar characterization showed that RPM-B-Mg/Al-LDHs had enhanced texture and surface chemistry linked to the formation/deposition of Mg- and Al-based nanoparticles. In addition, this biochar exhibited the highest P recovery rate from effluents (78 mg g−1). This recovery process seems to occur heterogeneously on multilayers through electrostatic interactions, ligand exchange, surface precipitation as AlPO4 and Mg3(PO4)2, and complexation. Phosphorus desorption from these P-loaded biochars was significantly dependent on the pH of eluent solutions with the highest desorption yield observed at an initial pH of 9.0 (88%). All these findings indicate that the use of Mg/Al-LDHs-loaded poultry manure biochar can be considered a sustainable material for P recovery from aqueous solutions. Furthermore, the P-loaded biochar could be reused in agriculture as a low-cost biofertilizer in P-depleted soils. [ABSTRACT FROM AUTHOR]

Calcium sulfate whiskers (CSW) exhibit significant surface polarity and high surface energy, leading to aggregation when directly incorporated into polymer matrices, significantly affecting the mechanical properties of the composites. Sodium oleate (SO) was used to modify CSW, introducing –C=C– active groups on the surface, followed by in‐situ graft polymerization of sodium oleate‐modified CSW (SO‐CSW) with methyl methacrylate (MMA) to prepare CSW‐g‐PMMA composites. The modification mechanism of SO and PMMA on CSW, as well as the surface modification effects on CSW, were studied using DRIFT, XRD, XPS and TEM. The results show that oleic acid ions adsorb onto the surface of CSW in two forms. One is chemisorption, in which the oleic acid ions are adsorbed on the calcium ions site on the surface of CSW in a bridging way. The other is physical adsorption, oleic acid ions and dissolved calcium ions in the form of precipitation adsorbed on the outermost layer of CSW. After in‐situ polymerization, PMMA was successfully grafted onto the surface of CSW, and the thickness of the surface PMMA coating layer was approximately 67 nm. CSW‐g‐PMMA was used as a filler in the melt blending with polypropylene (PP) to prepare PP composites. CSW‐g‐PMMA mainly toughens and enhances the mechanical properties of PP composites in the form of crack bridging, crack deflection and pull‐out effect. Highlights: The mechanism of sodium oleate modified calcium sulfate whisker (CSW) has been investigated. One is chemical adsorption that the oleic acid ions are adsorbed on the calcium ions site on the CSW surface in a bridge way. The other is physical adsorption that oleic acid ions and dissolved calcium ions are adsorbed in the form of precipitation on the outer layer of CSW.After the modification of sodium oleate, the active group –C=C– was introduced on the surface of CSW, and then the PMMA long chain polymer was grafted with an in‐situ polymerization to form a PMMA coating layer with a thickness of about 67 nm, which significantly improved the hydrophobicity of CSW surface.After modification with sodium oleate and PMMA grafting, the modified CSW significantly toughened and enhanced the mechanical properties of PP composites in the form of crack bridging, crack deflection and pull‐out effect. [ABSTRACT FROM AUTHOR]

Due to its high thermal conductivity, graphene finds extensive application in thermal composite materials. However, akin to polymer composites containing other fillers, the thermal resistance at the interface between graphene and the polymer matrix substantially impedes heat conduction. Thus, functionalizing graphene becomes imperative to enhance its dispersibility in polymers. In this study, we synthesized the imidazolyl ionic liquid 1‐methyl‐3‐triethoxysilpropyl imidazole chloride ([MTESiPIM]Cl). Ionic liquid complexes supported by graphene (G) were synthesized via a simple ultrasonic stripping method by combining electrochemical graphene (G) with [MTESiPIM]Cl (Si‐IL@G). The Si‐IL@G/LLDPE composite was formed by blending Si‐IL@G into the linear low‐density polyethylene (LLDPE) matrix using a melt blending technique. Upon adding 5% Si‐IL@G, the tensile strength and bending modulus of Si‐IL@G/LLDPE composite reached 13.5 MPa and 348.2 MPa, respectively, marking an increase of 20.67% and 57.79% over pure LLDPE. The Si‐IL@G/LLDPE composite exhibited a thermal conductivity of 0.49 W·m−1·K−1, 96.0% higher than that of pure LLDPE. Given its outstanding thermal conductivity and mechanical properties, Si‐IL@G holds great potential in producing composites with high thermal conductivity. Highlights: An ionic liquid with siloxanyl groups was synthesized using microwave assistance.The ionic liquid was modified onto graphene sheets using ultrasonic techniques.The study examined how ionic liquid‐modified graphene affects LLDPE structure.The thermal conductivity and mechanical properties of LLDPE were enhanced. [ABSTRACT FROM AUTHOR]

Recent surface-enhanced Raman spectroscopy (SERS) developments involve using nonmetallic materials as substrates. Molybdenum disulfide (MoS2) is a notable nonmetal semiconductor surface-enhanced Raman scattering (SERS) substrate because of its low cost, abundance, remarkable stability, and considerable chemical activity. However, its limited SERS activity has significantly impeded its advancement in SERS research. Herein, we report a facile and efficient approach for rapidly producing monolayer MoS2 films with adjustable sulfur vacancies via nitrogen plasma treatment. Monolayer MoS2 films exhibit exceptional sensitivity for SERS detection by manipulating the vacancy density. The optimized MoS2 substrate achieved a detection limit of roughly 10–10 M and an enhancement factor of 2.29 × 105 for rhodamine 6G (R6G) probe molecules. We further illustrated that introducing sulfur vacancies can alter the bandgap structure of MoS2, thereby facilitating the separation of internal charge carriers and intensifying interactions with the target components. The vacancy-assisted technique paves the path for the widespread use of semiconductor-based ultrasensitive molecular detection. [ABSTRACT FROM AUTHOR]

The persistent reliance on coal has resulted in the accumulation of substantial coal gangue, a globally recognized problematic solid waste with environmental risks. Given the coal gangue properties and global land degradation severity, the resourceful utilization of coal gangue as soil conditioners is believed to be a universally applicable, cost-effective, high-demand and environment-friendly model with broad application prospect. The direct application of raw coal gangue faces challenges of low active beneficial ingredients, inadequate water and fertilizer retention, presence of potentially toxic elements, resulting in limited efficacy and environmental contamination. This paper provided a comprehensive review of various modification methods (including mechanical, chemical, microbiological, thermal, hydrothermal and composite modifications) employed to enhance the soil improvement performance and reduce the environmental pollution of coal gangue. Furthermore, an analysis was conducted on the potential application of modified coal gangue as a muti-function soil conditioner based on its altered properties. The modified coal gangue is anticipated to effectively enhance soil quality, exhibiting significant potential in mitigating carbon emissions and facilitating soil carbon sequestration. This paper provided innovative ideas for future research on the comprehensive treatment of coal gangue and restoration of degraded soil in order to achieve the dual goals of zero-coal gangue waste and sustainable agriculture. [ABSTRACT FROM AUTHOR]

Surface, interface, and subsurface in catalysts are broadly perceived as independent units in materials, relying on diverse bonding environments and are recurrently studied discretely because of experimental challenges in distinguishing the surface and subsurface effects. Metal crystals, isolated atoms, or metal nanoparticles in supported catalysts induce an electrophilic nature in subsurface, enhancing the catalysis efficiency. In this review, the influence of modification in subsurface of catalysts and their specific catalytic outputs are discussed. Key approaches and techniques for insertion of subsurface modifications and impact of electrophilicity upon catalysis upgradation are observed. A compilation of frequently used chemical reactions catalyzed by subsurface‐modified catalysts have been structured and thoroughly illustrated. [ABSTRACT FROM AUTHOR]

Owing to the toxicity and widespread use of copper, the pollution caused by copper ions has become a long-standing environmental and industrial challenge. In this study, a new adsorbent was developed to dispose of and remove copper ions from water. The modified chitosan–carboxymethyl starch (MCTS-CMS) polymer was characterised, and FTIR and SEM-EDS confirmed the successful graft modification of the receptor. The adsorption behaviour was investigated through various parameters, and the results showed that the optimal parameters were pH > 4.0, an adsorption time of 30 min, a reaction temperature of 293 K, and an initial concentration of 100–120 mg/L. The experimental data exhibited a good fit with pseudo-second-order models, and the Langmuir isotherm revealed that the polymer was found to be highly suitable for adsorption, with a maximum adsorption capacity of 321.16 mg/g. Thermodynamic analysis revealed that the adsorption process was exothermic and spontaneous. XRD and XPS confirmed the generation of posnjakite after the adsorption and the predominant roles of nitrogen- and sulphur-containing groups in the adsorption. Further analysis confirmed the existence of chemisorption and physical adsorption, with chemisorption mainly facilitating the Cu(II) absorption of the polymer. MCTS-CMS showed an excellent removal efficiency of 98% in acidic solutions. On the basis of these findings, the MCTS-CMS polymer demonstrates excellent performance and high selectivity in the removal of copper ions from industrial wastewater or polluted water bodies. This work recommends expanding the polymer's practical applications to contribute to water purification efforts. [ABSTRACT FROM AUTHOR]

Nanocellulose is a robust material with a broad spectrum of potential applications. Manufacturing nanocellulose has garnered greater interest recently and is currently the European economy's second-highest priority. It is possible to extract from plants' biomass using various methods, which are divided broadly into various categories. The kind of biomass, the desired qualities of the nanocellulose, and the production size all have a role in selecting the pretreatment and extraction process. Several pretreatment and extraction techniques for nanocellulose from plant biomass are covered in this review, along with the variables that affect method selection. Developing scalable, effective production processes for nanocellulose is crucial for commercializing technologies. The current processes to create nanocellulose are still somewhat inefficient, and industrial scale-up is challenging. Future studies are likely to focus on efficient, scalable techniques for reducing down cell walls from plants and lower-cost nanocellulose synthesis using clean energy sources. [ABSTRACT FROM AUTHOR]

For concrete structures in marine or groundwater environments, sulfate attack is a major factor contributing to the degradation of concrete performance. This paper analyzes the existing literature on the chemical reactions and physical crystallization effects of sulfate attack on cement-based materials, summarizing the degradation mechanisms of corroded concrete. Experiments have been conducted to study the performance evolution of concrete under sulfate attack, considering both external environmental factors and internal factors of the cement-based materials. External environmental factors, such as the temperature, humidity, concentration, and type of sulfate solutions, wet-dry cycles, freeze-thaw cycles, chloride coupling effects, and stray currents significantly impact sulfate attack on concrete. Internal factors, including internal sources of corrosion, the chemical composition of the cement, water-cement ratio, and the content of C-S-H gel and Ca(OH)2, influence the density and sulfate resistance of the cement-based materials. Additionally, five typical methods for enhancing the sulfate resistance of concrete are summarized. Finally, the paper identifies current challenges in the study of corroded concrete and proposes directions for future research. [ABSTRACT FROM AUTHOR]

Objectives Methods Results Conclusions One of the main advantages of the hinotori™ surgical robot system (HSRS) is that it can be easily adjusted. This study aimed to clarify the effects of modifying the HSRS on the perioperative outcomes of robotic‐assisted radical prostatectomy (RARP).Overall, 158 cases of RARP using the HSRS were classified into three groups based on the modification to the system: group A (no modification, 70 cases), group B (addition of the ability to switch between two types of scopes and to adjust the arm base tilt back and forth, left and right, 42 cases), and group C (reduction of arm floating sensation, mitigation of emergency stop during arm collision, and addition of clutch function via hand switch in addition to foot pedal, 46 cases). The perioperative outcomes of each group were compared.The median of operation time, cockpit time, and cockpit time excluding the time required for lymph node dissection of group C were 223, 146, and 135 min, respectively, where are significantly shorter than those of group A (308, 228, and 208 min, p < 0.0001, respectively) and group B (319, 241, and 214 min, p < 0.0001, respectively). There was no significant difference in the rate of positive margin rates and the pad‐free rate before the first follow‐up visit among these three groups. The complication rates in groups A, B, and C were 11.4%, 9.4%, and 8.4% (Clavien‐Dindo grades I–II), and 4.3%, 2.4%, and 0% (grade III), respectively.The modifications to the HSRS have enabled smoother surgical procedures for RARP. [ABSTRACT FROM AUTHOR]

Background and Objectives The Individualized Positive Psychosocial Interaction (IPPI) program is an adaptable, evidence-based intervention. IPPI trains nursing home care partners to engage residents living with moderate to severe dementia in preference-based, one-to-one interactions using emotion-focused communication. We sought to understand provider-driven adaptations made to the IPPI program and whether the adaptations made were fidelity-consistent. Research Design and Methods Data were collected from n = 78 interviews with n = 23 nursing home provider champions who led a quality improvement project to implement the IPPI program with 3–5 residents per care community. Using content analysis, we report quantitative data on the adaptation characteristics according to the Framework for Reporting Adaptations and Modifications-Expanded core modules and participant quotes to illustrate adaptations. Results Champions reported 34 adaptations, with an average of 2.6 adaptations per nursing home. The majority of IPPI adaptations pertained to implementation (65%; n = 22), whereas 17% (n = 6) were content and 17% (n = 6) were context. Some adaptations were motivated by the organization (e.g. time constraints), while others were motivated by the recipient (e.g. cognitive capacity). Most adaptations made to the IPPI protocol by care partners were fidelity-consistent (92%; n = 33). Discussion and Implications Care partners' adaptations to the IPPI made the intervention more resident-centric. Future healthcare intervention providers must consider the user perspective and encourage adaptations that further tailor to the user, as long as the adaptations are fidelity-consistent. [ABSTRACT FROM AUTHOR]

Reducing the dependence of epoxy resin preparation on petroleum resources and developing thermosetting epoxy resins with excellent comprehensive performance are important directions for the current development of epoxy resins. This article uses biomass resource magnolol as the main raw material to prepare magnolol epoxy monomer (DGEM). Then, using 4,4-diaminodiphenylmethane (DDM) as the curing agent, the DGEM and bisphenol A epoxy resin (E44) were blended and cured. The results showed a dual modification effect of DGEM on the toughening and strengthening of E44 epoxy resin. When the mass ratio of DGEM to E44 is 30:70, the bending strength of the cured blended resin is 18.7% higher than that of the E44 system, and the tensile strength is 57.7% higher. When the mass ratio of DGEM to E44 is 5:95, the cured blended resin exhibits the optimal impact strength (5.10 kJ/mol), which is 22.9% higher than the pure E44 system. However, the addition of DGEM reduced the glass transition temperature and crosslinking degree of the blended resin system. The addition of DGEM improves the heat resistance and flame retardancy of the blended resin. When the mass ratio of DGEM: E44 was 50:50, the vertical combustion reached UL-94 V-0 level. [ABSTRACT FROM AUTHOR]

Acid mine drainage (AMD) is an environmental concern, and its discharge into the surrounding environment can lead to acidification of water bodies and soil. In this research, red mud (RM) with alkaline pH as aluminum industry waste was implemented as an adsorbent for sulfate removal, which can be available in AMD and adsorption processes as an influential method was applied for AMD treating. Seawater washing (BRM), acid treatment (HRM), and composition with chitosan (CRM) were employed as RM modification methods. Various analytical methods were applied, including x-ray fluorescence spectroscopy (XRF), Fourier-transform infrared spectroscopy (FTIR), Brunauer Emmett Teller (BET), inductively coupled plasma analysis, and zeta potential, to have a clear comprehension of the sulfate adsorption behaviors and performance of activated methods. These methods have had desirable effects on the sulfate adsorption and adsorption amount, which range from 1.1 mg g−1 for RM reached to 13.4, 39.7, and 67.4 mg g−1 for BRM, HRM, and CRM, respectively. XRF results demonstrated a decrease in calcium and sodium ion amounts that can occur due to their dissolution in the acidic solution. It can create the active surface areas for adsorption onto RM with acid washing. Based on FTIR results, sharp intensity vibration was observed in BRM, HRM, and CRM after sulfate adsorption in the 1,100 cm−1 band that is approximately related to SO42− vibration. BRM porosity decreased from 0.0686 to 0.0345 cm3 g−1 due to various salts' precipitation in seawater, but the porosity volume and specific surface area increased for HRM from 0.0686 to 0.184 cm3 g−1 due to dissolution of ions in HCl. In addition, zeta potential increased to positive amounts from 2.7 to 3.4, 3.8, and 4.5 mv for BRM, HRM, and CRM, respectively. Langmuir isotherm indicated that the highest adsorption amount (qm) as a calculated parameter for BRM, HRM, and CRM was 0.88, 2.45, and 18.6 mg g−1 , respectively. Among modification methods, combination RM and chitosan had the highest impact and increases sulfate removal and adsorption amount at lower pH levels due to further positive charge on the CRM surface. [ABSTRACT FROM AUTHOR]

In this paper, the results of the technological combustion of SHS heat insulators based on mineral origins are presented. It is shown that after mechanochemical treatment of minerals—diatomite—the kinetic characteristics of the combustion process change, providing targeted formation of the phase composition, structure, and properties of the SHS composite. A positive effect of using various modifiers during the MCT of diatomite—the activation of the combustion process—was established. The selection of modifiers provides an increase in the strength of the synthesized SHS composites as a result of the formation of aluminate compounds in the synthesis products, and a decrease in thermal conductivity to 0.157 W/m*K due to the formation of the ultraporous structure of the samples. [ABSTRACT FROM AUTHOR]

Zinc-based batteries (ZBBs) have proven to be tremendously plausible for large-scale electrochemical energy storage applications due to their merits of desirable safety, low-cost, and low environmental impact. Nevertheless, the zinc metal anodes in ZBBs still suffer from many issues, including dendrite growth, hydrogen evolution reactions (HERs), corrosion, passivation, and other types of undesirable side reactions, which severely hinder practical application. The modification of Cu-based current collectors (CCs) has proven to be an efficient method to regulate zinc deposition and prevent dendritic growth, thereby improving the Coulombic efficiency (CE) and lifespan of batteries (e.g., up to 99.977% of CE over 6900 cycles after modification), which is an emerging research topic in recent years. In this review, we provide a systematic overview of the modification of copper-based CCs and their application in zinc metal anodes. The relationships between their modification strategies, nano-micro-structures, and electrochemical performance are systematically reviewed. Ultimately, their promising prospects for future development are also proposed. We hope that this review could contribute to the design of copper-based CCs for zinc-based batteries and facilitate their practical application. [ABSTRACT FROM AUTHOR]

For many decades, natural and modified clay minerals have been used as adsorbents to clean up aquatic and soil ecosystems contaminated with organic and inorganic pollutants. In this study, organoclays based on bentonite and various amphoteric and nonionic surfactants were synthesized and tested as effective sorbents for lead ions. The maximum values of R were obtained when describing the sorption processes using the Langmuir model, which ranged from 0.97 to 0.99. The adsorption of lead ions by these organoclays was investigated using different sorption models including the Langmuir, Freundlich, and BET. It was found that, according to the values of limiting adsorption to the Langmuir equation, the synthesized organoclays formed an increasing series: organoclay with cocamide diethanolamine < bentonite < organoclay with lauramine oxide < organoclay with sodium cocoiminodipropionate < organoclay with disodium cocoamphodiacetate < organoclay with alkyl polyglucoside. The Gibbs energy for all of the analyzed samples was calculated and found to be negative, indicating the spontaneity of the cation adsorption process in the forward direction. The maximum value of the adsorption capacity of lead cations on organoclay-based bentonite with alkyl polyglucoside was 1.49 ± 0.05 mmol/g according to the Langmuir model, and 0.523 ± 0.003 mmol/g as determined by the BET model. In the process of modifying bentonite, there was an increase in negative values of the zeta potential for organoclays compared to the initial mineral, which clearly enhanced their electrostatic interactions with the positively charged lead ions. It was hypothesized, based on the physicochemical principles, that exchange adsorption is the main mechanism for lead absorption. Based on chemical approaches, organoclays based on amphoteric surfactants absorb lead mainly through the mechanisms of electrostatic attraction, ion exchange, and complexation as well as the formation of insoluble precipitates. Organoclays based on nonionic surfactants, on the other hand, absorb lead through mechanisms of complexation (including chelation) and the formation of insoluble chemical precipitates. The comparison of isotherms from different models allows us to find the most accurate match between the model and the experimental data, and to better understand the nature of the processes involved. [ABSTRACT FROM AUTHOR]

The impact of various modification methods on enhancing the adsorption performance of coal gangue (CG) for hazardous heavy metals has not been thoroughly investigated. In this study, three CG samples were first modified by calcination, followed by acid washing, alkali washing, and hydrothermal treatment, to obtain modified CG samples. The adsorption performance was assessed based on the adsorption capacities for Cd2⁺ and Pb2⁺ (i.e., qe,Cd and qe,Pb), and the kinetics of the adsorption processes were analyzed using kinetic equations. XRD, SEM-EDX, FTIR, and N2 adsorption–desorption isotherms were used to elucidate the adsorption mechanisms. Results indicated that qe,Cd and qe,Pb of raw CG samples were approximately 10 and 25 mg/g, respectively, with only slight changes observed after calcination, acid washing, and alkali washing. In contrast, hydrothermal treatment yielded NaP and NaA zeolites, which significantly enhanced qe,Cd and qe,Pb to values of 48.5–72.7 and 214.9–247.5 mg/g, respectively. The hydrothermally treated CG samples primarily adsorbed Cd2⁺ and Pb2⁺ through ion exchange with Na⁺ within the zeolite structure, facilitating the entry of these ions into the zeolite's pore channels. The adsorption processes were effectively described by the pseudo-second-order kinetic model. By optimizing the conditions of hydrothermal modification, the adsorption performance of CG samples is anticipated to further improve due to the creation of additional adsorption sites. [ABSTRACT FROM AUTHOR]

Copyright of Acta Materiae Compositae Sinica is the property of Acta Materiea Compositae Sinica Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

This study aimed to find out the distribution, destructions, developments, transformations, and processes of changes of mosques after WWII in Herat Old City, which is a medieval city still preserved and standing. One hundred and eight mosques were constructed, 2 of them were demolished, and 106 still exist. Twenty-eight are modern mosques, and 80 are traditional. Twenty-two out of 80 are preserved, 56 have been transformed, and 2 were damaged, or demolished. Modern mosques are mainly located in the second and fourth quarters, while traditional mosques are distributed in all four quarters. The transformation started in the 1950s after WWII, continued in the 1970s, 1990s, and 2000s, and has occurred in all four quarters, slightly higher in the second and fourth quarters. Through a field survey, data were collected, findings were combined, unified, and plotted on the map, and the mosques were categorized based on building material. [ABSTRACT FROM AUTHOR]

The doping process is a unique method of changing the microstructure of a material, influencing its mechanical, thermal, and optical properties. Typically, the doping process is carried out via chemical reagents. In this work, we present a "green" method of doping photochromic TiO2 via low-temperature plasma. The doping agent was the electrode material that was sputtered during plasma burning. The process of electrode sputtering is confirmed by the emission spectroscopy data of the plasma zone and the mass loss of the electrodes. The doping process was confirmed by X-ray, Raman spectroscopy, and XPS analyses. The role of the dopant nature and the action of diaphragm discharge in improving the photochromic properties of titanium dioxide is considered. [ABSTRACT FROM AUTHOR]

Silica serves as the primary filler in the fabrication of eco‐friendly tires, and achieving an optimal dispersion of polar silica within the natural rubber matrix is crucial for crafting high‐performance rubber composites. In this study, biodegradable surfactants polyethylene glycol (PEG) with molecular weights of 200, 400, and 800 were employed to modify silica. The modified silica was characterized by Fourier‐transform infrared spectroscopy; PEG‐modified silica with different molecular weights was compounded with Si69, a conventional silane coupling agent, in the formulation. This aimed to reduce Si69 dosage and mitigate the emission of volatile organic gases, such as ethanol, generated during the silanization reaction between Si69 and silica. Experimental findings revealed that compared with natural rubber composites containing six parts of Si69, the addition of PEG‐modified silica enhanced filler dispersion in the composite while reducing Si69 dosage by three parts. This led to accelerated vulcanization rates, effectively decreased energy consumption during production, and significantly improved wet slip resistance, while maintaining optimal rolling resistance. Rubber composites prepared with PEG800‐modified silica exhibited a 10% increase in elongation at break, a 12% increase in tensile product coefficient, and a 19% enhancement in wet slip resistance. Highlights: Silica is modified by polyethylene glycol with molecular weight of 200, 400, and 800.The amount of silane coupling agent and VOC emissions are reduced.The interfacial bonding between silica and rubber matrix is enhanced.The tensile product coefficient and wet slip resistance are improved by 12% and 19%. [ABSTRACT FROM AUTHOR]

Activated carbon (AC) adsorption is commonly used for polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) removal from flue gas. However, the AC available in the market predominantly possesses a substantial specific surface area and numerous micropores leading to significant variations in their adsorption characteristics. In this study, three types of activated carbon (AC) impregnated with different activating agents, namely K2CO3, KOH, and H3PO4 were evaluated for their effectiveness in removing PCDD/Fs and dl-PCBs compounds. For dl-PCBs, AC impregnated with H3PO4 resulted in a substantial reduction of PCB concentrations with an impressive 98% reduction achieved. Impregnation with KOH proved even more effective attaining a remarkable 99% reduction. In contrast, impregnation with K2CO3 while still effective achieved a slightly lower reduction rate of 95%. For PCDD/F, LACH3PO4 showed selectivity in achieving high reductions across both CDD and CDF congeners however proved effective in reducing the ∑PCCDF from 403.94 ng/Nm3 to 3.463 ng/Nm3 and ∑TEQ from 41.34 ng I-TEQ/Nm3 to 0.35 ng I-TEQ Nm3. LACKOH proved effective in reducing the ∑PCCDF from 540.45 ng/Nm3 to 0.25 ng/Nm3 and ∑TEQ from 57.42 ng I-TEQ/Nm3 to 0.12 ng I-TEQ Nm3 obtaining the overall removal efficiency of 99.5%. While the LACKOH injections were successful in the absorption of PCDD/Fs from the gas phase, it was observed that certain PCDD/F congeners became desorbed and entrapped within the ash necessitating further treatment of the ash residue. The ash underwent a thermal treatment first at 300 °C and 500 °C. The thermal treatment at 500 °C achieved a remarkable degradation of 99.7% removal efficiency rendering the ash and residue safe for disposal in a landfill site.Article Highlights: The study assessed K2CO3, KOH, and H3PO4 for AC activation efficiency. KOH proved most effective (99.5% removal). Post-ash treatment at 500 °C degraded PCDD/Fs by 99.7%, ensuring safe landfill disposal. [ABSTRACT FROM AUTHOR]

Copyright of Hydrometallurgy of China is the property of Hydrometallurgy of China Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Composite zirconium–titanium–silica sorbents with SiO2 content of 10–30 wt % were synthesized on the basis of products of hydrochloric acid decomposition of eudialyte concentrate and their surface modification into H+ and Na+ forms was carried out. All samples were studied by methods of chemical, X‑ray phase, Brunauer–Emmett–Teller (BET), and Barrett–Joyner–Halenda (BJH) analyses. It is shown that all obtained samples of silica-containing Zr–Ti–SiO2 sorbents are mesoporous. The pores are predominantly wedge-shaped with open ends, and pores with a diameter of 10–50 nm (~50% of the total pore volume) have the maximum volume. Based on the obtained values of the specific capacity of the adsorption monolayer of the surface of SiO2 samples and the value of Gibbs energy change (ΔG°) in the process of nitrogen sorption, it was concluded that the surface modification of synthesized Zr–Ti–SiO2 sorbents does not affect the physicochemical properties of their surfaces and the mechanism of nitrogen sorption. The sorption activity of synthesized samples towards Cu2+, Co2+, and Sr2+ ions was studied by the static method. It was found that modification of the obtained samples into the H+ form has less influence on their sorption capacity than their conversion into the Na+ form, does not depend on their SiO2 content in the range of 10–30%, and decreases in the Cu2+ → Co2+ → Sr2+ series. [ABSTRACT FROM AUTHOR]

New technologies of microelectronics are emerging to reduce the size of devices and combine them into more compact ultralow power systems. Betavoltaic power sources (BVPSs) can serve as power generators of such order. BVPSs consist of a combination of betavoltaic cells (BVCs) based on long-lived radioisotopes of beta radiation and semiconductor converters (SCs). One of the key tasks for increasing the power of BVCs is the selection of SCs that can efficiently convert the energy of beta particles into electricity. Currently, semiconductor structures with a developed surface and a high band gap are considered to be perspective SCs. In present work, arrays of titanium dioxide nanopores (TiO2 NPs) synthesized by common electrochemical anodization were chosen as a SCs. These SCs were part of BVCs based on nickel-63 with an activity of ~10 Ci/g. TiO2 NPs with an amorphous structure in the composition of BVC demonstrated low electrical parameters. To increase them, we modified TiO2 NPs by the hydrothermal method in a solution of Sr(OH)2 with a concentration of 0.05 mol/L at various times. These experiments were carried out in order to convert TiO2 (anatase) into structure-like SrTiO3. We found that the electrical parameters of the SCs increased with the duration of the modification time. The best result was obtained in the case of modification for 3 h—the BVC generated a short circuit current of 2.9 nA and open circuit voltage of 0.8 V and had a maximum power of 0.8 nW at 0.45—0.5 V. The obtained electrical parameters in combination with the miniature dimensions of the BVCs open up the potential possibility of creating a BVPS with an increased power density. [ABSTRACT FROM AUTHOR]

Backgrounds: Acute transplant rejection is a major component of poor prognoses for organ transplantation. Owing to the multiple complex mechanisms involved, new treatments are still under exploration. Endometrial regenerative cells (ERCs) have been widely used in various refractory immune-related diseases, but the role of ERC-derived exosomes (ERC-Exos) in alleviating transplant rejection has not been extensively studied. Signaling lymphocyte activation molecule family 6 (SLAMF6) plays an important role in regulating immune responses. In this study, we explored the main mechanism by which ERC-Exos loaded with siSLAMF6 can alleviate allogeneic transplant rejection. Methods: C57BL/6 mouse recipients of BALB/c mouse kidney transplants were randomly divided into four groups and treated with exosomes. The graft pathology was evaluated by H&E staining. Splenic and transplanted heart immune cell populations were analyzed by flow cytometry. Recipient serum cytokine profiles were determined by enzyme-linked immunosorbent assay (ELISA). The proliferation and differentiation capacity of CD4+ T cell populations were evaluated in vitro. The α-2,6-sialylation levels in the CD4+ T cells were determined by SNA blotting. Results: In vivo, mice treated with ERC-siSLAMF6 Exo achieved significantly prolonged allograft survival. The serum cytokine profiles of the recipients were significantly altered in the ERC-siSLAMF6 Exo-treated recipients. In vitro, we found that ERC-siSLAMF6-Exo considerably downregulated α-2,6-sialyltransferase (ST6GAL1) expression in CD4+ T cells, and significantly reduced α-2,6-sialylation levels. Through desialylation, ERC-siSLAMF6 Exo therapy significantly decreased CD4+ T cell proliferation and inhibited CD4+ T cell differentiation into Th1 and Th17 cells while promoting regulatory T cell (Treg) differentiation. Conclusions: Our study indicated that ERC-Exos loaded with siSLAMF6 reduce the amount of sialic acid connected to α-2,6 at the end of the N-glycan chain on the CD4+ T cell surface, increase the number of therapeutic exosomes endocytosed into CD4+ T cells, and inhibit the activation of T cell receptor signaling pathways, which prolongs allograft survival. This study confirms the feasibility of using ERC-Exos as natural carriers combined with gene therapy, which could be used as a potential therapeutic strategy to alleviate allograft rejection. [ABSTRACT FROM AUTHOR]

The country's first tubular microfiltration membranes for water purification from various contaminants, made from an alternative natural material—wood,—was developed at the Dumansky Institute of Colloid and Water Chemistry of the National Academy of Sciences of Ukraine. The proposed procedure cuts significantly the costs of manufacturing membranes. They studied the main patterns of the defluoridation process of water using these lignocellulosic (wooden) membranes, which were modified with a dynamic layer of hydrophilic A-300 aerosil. The modification of the lignocellulosic membranes involved the preliminary formation of an additional retentive layer on their surface, due to the steric mechanism, in the form of a dynamic membrane. The research demonstrated the high efficiency of the water defluoridation process using a dynamic membrane made of SiO2 particles, which retained fluoride ions (F–) ions due to the electrostatic mechanism of their interaction. Specific conditions for forming the dynamic membrane included concentrations of modifying and membrane-supporting aerosil additives at 500 and 100 mg/dm3, respectively, with an operating pressure of 1.0 MPa and a formation duration of 120 min. The concentration of suspended SiO2 particles in the permeate (turbidity) did not exceed the maximum permissible concentration (0.3 mg/dm3) in water. The modified lignocellulosic membrane could decrease the fluoride concentration in water to the permissible level for drinking water (0.7–1.5 mg/dm3) from an initial concentration of up to 7.5 mg/dm3 and a neutral pH at an operating pressure of 1.0 MPa. The membrane's specific productivity was 0.024 m3/(m2 h), due to significant pore blockage by SiO2 particles. [ABSTRACT FROM AUTHOR]

Rice husk biochar is a low-cost carbonaceous adsorbent; however, it has low adsorption capacity. To increase its potential application, biochar should be modified to enhance its porous structure and surface adsorptive sites for better adsorption performance. In this study, a hydrothermal process has been proposed to modify rice husk biochar and evaluate its effect on the structure and rhodamine B adsorption performance. Upon the hydrothermal treatment, surface area and porosity increased significantly from 54.1 m2/g and 0.04 cm3/g to 104.7 m2/g and 0.08 cm3/g, respectively and as result, its adsorption capacity improved by 98.6%. Biochar showed a good adsorption performance in a wide range of pH from 2 to 10 with maximum adsorption at pH = 2.7. Rhodamine B adsorption fits well the Langmuir isotherm model and pseudo-second order kinetic model, that underlines chemical interaction as a major adsorption mechanism. Additionally, hydrothermal treatment improved the recyclability of biochar with only ~ 5.5% loss in the adsorption capacity of modified biochar compared with 33.7% loss of unmodified sample. The addition of ZnCl2 as catalyst in hydrothermal process does not improve the adsorption performance of modified biochar. This work demonstrated that hydrothermal modification is not only an effective but also green method to improve the adsorption performance of rice husk biochar. [ABSTRACT FROM AUTHOR]

Objective: Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease. Research indicates that N6-methyladenosine (m6A) modification plays a crucial role in cellular autophagy during ALS development. This study investigates the role of autophagy in ALS, with a focus on the effect of messenger ribonucleic acid m6A methylation modification on disease progression. Material and Methods: We compared m6A levels and regulatory molecule expressions in transgenic superoxide dismutase (SOD1)-G93A and non-transgenic mice, categorized into end-stage and control groups, using quantitative polymerase chain reaction and Western blotting. The NSC-34 cell line, which was modified to model ALS, enabled the investigation of apoptosis, autophagy, and autophagy disruption through terminal deoxynucleotidyl transferase deoxyuridine triphosphate nick-end labeling assays, Western blotting, and fluorescent staining. Results: Our findings indicate significantly elevated m6A methylation levels in ALS mice (0.262 ± 0.005) compared with the controls (0.231 ± 0.003) and in the ALS model cells (0.242±0.005) relative to those belonging to the wild-type control group (0.183 ± 0.007). Furthermore, the proteins involved in m6A RNA modification differed between groups, which suggest impaired autophagy flux in the ALS models. Conclusion: These results suggest that m6A methylation may accelerate ALS progression through the disruption of autophagic processes. Our study underscores the role of m6A methylation in the pathology of ALS and proposes the targeting of m6A methylation as a potential therapeutic strategy for disease treatment. Although this study primarily used transgenic SOD1-G93A mice and NSC-34 cell models to investigate ALS pathology, potential differences in disease mechanisms between animal models and humans must be considered. Although a correlation was detected between m6A methylation levels and autophagy disruption in ALS, the study primarily established an association rather than provided detailed mechanistic insights. [ABSTRACT FROM AUTHOR]

An ever-increasing number of applications of oxide aerogels places a high demand on wettability-tuning techniques. This work explores the possibility to cheaply prepare GeO2 aerogels with controlled wettability by an ambient pressure drying (APD) method. GeO2 aerogels are prepared via two synthetic routes. Surface modification is carried out by soaking the gels in a silylating agent solution; type and concentration of the modifier are optimized to achieve a large surface area. The aerogels have been characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, nitrogen adsorption and contact angle measurements. The effect of surface modification on the phase composition and particle size of the aerogels is described. In summary, the work provides a new cheap production method for the preparation of both hydrophobic and hydrophilic GeO2 aerogels with contact angle varying from 30° to 141° and with surface area of 90–140 m2/g, which facilitates the expansion of their diverse applications. GeO2 aerogel synthesis by APD is reported for the first time. [ABSTRACT FROM AUTHOR]

In biomaterials research, using one or two components to prepare materials is common. However, there is a growing interest in developing materials composed of three components, as these can offer enhanced physicochemical properties compared to those consisting of one or two components. The introduction of a third component can significantly improve the mechanical strength, biocompatibility, and functionality of the resulting materials. Cross-linking is often employed to further enhance these properties, with chemical cross-linking agents being the most widely used method. This article provides an overview of the chemical agents utilized in the cross-linking of three-component biomaterials. The literature review focused on cases where the material was composed of three components and a chemical substance was employed as the cross-linking agent. The most commonly used cross-linking agents identified in the literature include glyoxal, glutaraldehyde, dialdehyde starch, dialdehyde chitosan, and the EDC/NHS mixture. Additionally, the review briefly discusses materials cross-linked with the MES/EDC mixture, caffeic acid, tannic acid, and genipin. Through a critical analysis of current research, this work aims to guide the development of more effective and safer biopolymeric materials tailored for biomedical applications, highlighting potential areas for further investigation and optimization. [ABSTRACT FROM AUTHOR]

The Solid-State Linear Transformer Driver (SSLTD) is a nanosecond pulse power source characterized by its fast rise time and adjustable output waveform. It can generate uniform and stable atmospheric plasma jets, which is suitable for material surface modification. In this study, a 15-stage SSLTD was designed and assembled, which can produce a stable nanosecond pulse voltage up to 15 times the amplitude of the charging voltage at high frequencies, with a rise time of approximately 10 ns. This device can be used to generate stable atmospheric pressure Ar plasma jets with an electron density in the range of 1015~1016 cm−3 and gas temperatures close to room temperature. After the modification treatment by the plasma jets, the content of the C=O groups on the surface of the epoxy resin significantly increased in the wavelength range of 1720~1740 cm−1, and its flashover resistance was noticeably enhanced. The optimal comprehensive modification effect was achieved at a charging voltage of 600 V, pulse width of 50 ns, and pulse frequency in the range of 800~1000 Hz. [ABSTRACT FROM AUTHOR]

Alginate fibers made from seaweed have some desirable properties as textile materials, but they also have two shortcomings that limit their usages: they are intolerant to salt, alkali, and detergent, and they are difficult to dye due to the electrostatic repulsion with anionic dyes. To solve the two problems in this project, a process of successive modification of alginate fibers using sodium pyrophosphate, alum, and sodium hydroxide was developed. SEM images and ion content of the modified alginate fibers showed that the fibers did not dissolve in high concentrations of sodium chloride, sodium hydroxide, or standard detergent solution and still maintained their original morphology. Also, the results of FTIR, XPS, XRD, and single-fiber strength tests indicated that the modification process enabled the alginate fibers to form a new tetrahydroxy cross-linking structure and thus improved their mechanical properties. The tetrahydroxy cross-linking structure prevented the dissolution of alginate fibers by blocking the exchange of ions between the fibers and the solution. Besides, the presence of Al3+ in the tetrahydroxy cross-linking structure modified the electrostatic repulsion between the alginate fiber and the anionic dye, resulting in high dyeing and dye fixation rates. Thus, the modified alginate fiber can be dyed directly with common dyes without dissolution, solving the above-mentioned two problems. This can enormously expand the potential usages of alginate fibers and therefore has significant academic and practical implications. [ABSTRACT FROM AUTHOR]

Copyright of Science & Technology of Food Industry is the property of Science & Technology of Food Industry Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

As an electron transport layer (ETL) widely used in organic solar cells (OSCs), ZnO has problems with energy level mismatch with the active layer and excessive defects on the ZnO surface, which can reduce the efficiency of OSCs. Here, ZnO/ZrSe2 composite is fabricated by modifying ZnO with 2D ZrSe2. The XPS and first‐principles calculation (FPC) show that ZnO obtains electrons from ZrSe2 and forms interfacial dipoles toward the active layer, which decreases the work function of ZnO, thus reducing the interface barrier and favoring the collection of electrons in OSCs. At the same time, after ZrSe2 modification, the oxygen vacancy density on the ZnO surface decreases, thus improving the conductivity of ZnO. More importantly, the femtosecond transient absorption (Fs‐TA) shows that ZrSe2 selectively traps holes from the active layer, which prevents the holes from entering the ZnO, thereby reducing the probability of electron recombination. Finally, ZnO/ZrSe2 composite is used as a novel ETL in OSCs with PBDB‐T: ITIC, PM6:Y6 and PM6: L8‐BO as active layers, and obtaining 12.09%, 16.34%, and 18.24% efficiency, respectively. This study provides a method for the interface modification of ZnO, and further investigates the role of 2D nanosheets in the interface modification. [ABSTRACT FROM AUTHOR]

The application of pulsed electric field (PEF) in food processing, has gained significant attention as a key non-thermal method. Studies have shown that PEF can not only effectively inactivate common microorganisms in fruit and vegetable juices without affecting the organoleptic quality, but also effectively promote the food drying and extraction of active substances, as well as the modification of macromolecules can be effectively realized by PEF, promoting the circular economy and the reuse of processing wastes. Over the past few years, PEF technology has made substantial progress, transitioning from laboratory and pilot plant stages to large-scale industrial applications. Future research is essential to optimize PEF parameters (e.g. field strength, pulse duration) for different food materials to maximize efficiency and effectiveness, facilitating the broader adoption of PEF technology in the industry. Understanding the molecular mechanisms underlying PEF-induced changes in food composition is also crucial. Moreover, conducting more pilot studies will help address practical challenges, enhancing the technology’s suitability for industrial-scale applications. This paper aims to systematically review the achievements of the PEF technology in various fields of food processing over the past five years, detailing its working principles and addressing the challenges and future directions for its large-scale application. [ABSTRACT FROM AUTHOR]

Polyethylene terephthalate (PET) is a conventional packaging material. Its modification has attracted immense attention in the industry and academia. Here, office waste paper, white cardboard waste, and waste corrugated paper were first employed as raw materials for cellulose nanocrystal (CNC) extraction by acid hydrolysis. Thereafter, CNC/PET composite films with various CNC additions were prepared via a self‐assembly technique. The results revealed that the CNCs formed a self‐assembled film on the PET surface via the synergistic effect of the complex interactions among the CNCs as well as between the CNCs and PET. Moreover, the CNCs improved the barrier property of PET and decreased the oxygen and water vapor transmittances of CNC/PET by 30.7% and 21.7%, respectively. Additionally, the coating of the PET surface with 0.2 wt.% CNCs extracted from the waste paper decreased the surface wettability of PET, exhibiting application potentials in the hydrophobic modification of polymers. This study realized waste paper recycling and provided a basis for constructing self‐assembled functional films on PET surfaces. The findings and insights of this study could exhibit application potentials in the fields of waste recycling and packaging materials. Highlights: A functional cellulose nanocrystal (CNC) film is prepared from waste paper.Self‐assembled CNC is coated on a PET surface to form a CNC/PET composite film.The synergistic interactions among CNCs and between CNC and PET modified PET.The low addition of CNCs realized the efficiency modification of PET.The study achieves waste paper recycling and high‐value utilization. [ABSTRACT FROM AUTHOR]

Modified polyvinylidene chloride (PVDC) resin was prepared using octafluoropentyl methacrylate and trimethylolpropane trimethacrylate as modifying monomers through seeded emulsion polymerization. The successful incorporation of octafluoropentyl methacrylate into the PVDC resin was confirmed by Fourier transform infrared spectroscopy (FTIR) and X‐ray photoelectron spectroscopy (XPS) analyses. Scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and XPS were utilized to investigate the element distribution in the modified monomer emulsion and the mechanism of monomer modification. The results demonstrated that the fluorine monomer was reacted in the resin, and mainly concentrated on the surface of the resin. The addition of octafluoropentyl methacrylate and trimethylolpropane trimethacrylate improved the water resistance of the resin. Compared to unmodified PVDC resin, the contact angle of the modified PVDC resin increased from 89.46° to 109.51°, and the water resistance at room temperature increased from 120 to 500 h. Furthermore, the modified resin exhibited excellent mechanical properties, thermal stability, and storage stability. [ABSTRACT FROM AUTHOR]