Substrate Pretreatment Research Articles

Innovative Zinc Anodes: Advancing Metallurgy Methods to Battery Applications.

Aqueous zinc metal batteries (AZMBs) are emerging as a powerful contender in the realm of large-scale intermittent energy storage systems, presenting a compelling alternative to existing ion battery technologies. They harness the benefits of metal zinc's high safety, natural abundance, and favorable electrochemical potential (-0.762V vs Standard hydrogen electrode, SHE), alongside an impressive theoretical capacity (820mAhg-1 and 5655mAhcm-3). However, the electrochemical performance of ZMBs is impeded by several challenges, including poor compatibility with high-loading cathodes and persistent side reactions. These issues are intricately linked to the inherent physicochemical properties of the zinc metal anodes (ZMAs). Here, this review delves into the traditional methods of ZMAs production, encompassing extraction, electrodeposition, and rolling processes. The discussion then progresses to an exploration of cutting-edge methodologies designed to enhance the electrochemical performance of ZMAs. These methods are categorized into alloying, pre-treatment of substrate, advanced electrodeposition techniques, and the development of composite anodes utilizing zinc powder. The review offers a comparative analysis of the merits and drawbacks of various optimization strategies, highlighting the beneficial outcomes achieved. It aspires to inspire novel concepts for the advancement and innovation of next-generation zinc-based energy storage solutions.

Synergising hydrothermal pre-treatment and biological processes for enhancing biohydrogen production from palm oil mill effluent

The high quantity of nutrient-rich palm oil mill effluent (POME) waste in the industry will have a severe negative environmental impact and a high cost of treatment. However, POME waste could be converted into bioenergy via environmentally sustainable processes. Several studies have explored using hydrothermal carbonisation for solid biomass products in biofuel production, but the potential of the liquid phase produced during these processes has received less attention. Therefore, this study aims to assess the potential of biohydrogen production from treated POME as a substrate by hydrothermal process. This study is presented in two phases: the first phase involves substrate pre-treatment using a hydrothermal process to improve biomass properties at different temperatures, and the second phase explores the potential for biohydrogen production from treated POME through dark fermentation. Substrate pre-treatment was conducted at 180, 210, and 240 °C using 100 % raw POME. Next, the treated POME was incubated for biohydrogen production at 50 °C for 24 h. A microbial analysis was conducted to determine the most dominant species present in the sample. Our findings show that at 180 °C, the total chemical oxygen demand (COD) removal efficiency was 80 %, and acetic acid concentration was 28 %. Compared to raw POME, treated POME generated a maximum hydrogen yield and rate (HPR) of 52.19 mL H2 g−1 CODrem and 0.59 mL H2 mL POME−1 day−1 with a 2.32-fold and 1.59-fold increase, respectively. Meanwhile, Clostridium was a dominant bacterial species identified in the treated POME. These findings demonstrated the feasibility of implementing a hydrothermal process to treat POME and improve its biohydrogen production efficiency. The treated POME from the hydrothermal process is more homogenous and readily consumable by microorganisms used in dark fermentation. Hydrothermal pre-treatment could potentially increase the rate and efficiency of microbial digestion, leading to enhanced hydrogen production. The high COD removal efficiency during the process significantly reduces the environmental impact of POME discharge, and converting POME into a valuable resource through the hydrothermal and dark fermentation process aligns with sustainable waste management practices.

A deep eutectic solvent with a lignin stabilization and functionalization for lignocellulosic biomass pretreatment

This study synthesized a functional deep eutectic solvent (DES) using betaine and glyoxylic acid (GA) for lignocellulosic biomass pretreatment. The Betaine/GA DES pretreatment resulted a high delignification efficiency of 81.89% and xylan removal of 83.25% while preserving most of cellulose. During pretreatment, lignin was stabilized by GA, preventing its condensation and introducing carboxyl groups onto its molecular backbone. The GA stabilized lignin (GASL), with a high β-O-4 linkage content of 62.92%, was depolymerized for phenolic monomer production with a bio-oil yield of 55.40%. Additionally, the functional lignin was used as a surfactant for GASL-based O/W emulsion (GA-O/W emulsion) preparation. With 0.5% of lignin addition and an optimal O/W ratio of 6:4, the resulting GA-O/W emulsion exhibited a high cream index value of 100% and excellent storage stability without any phase transition or emulsion aggregation. When using the lignin to prepare curcumin-encapsulated microcapsules, a cumulative curcumin remaining of 74.19% under UV radiation and an extraordinary encapsulation efficiency of 62.86% were achieved. Furthermore, this DES pretreatment promoted enzymatic saccharification of the pretreated cellulose substrate, resulting in a glucose yield of 91.49%. After adding 15 wt% of the fibers in soft wood pulp for papermaking, the tear index, ring crush strength index, and tensile index of the produced paper-sheets reached 112.04%, 98.58%, and 83.55% of those of the pure softwood pulp papers, respectively.

Influence of surface pretreatment of steel substrate on the interfacial microstructure and tensile properties of laser Al/steel joints

The influence of surface-pretreatments, viz., subtractive manufactured (SMed), additively manufactured (AMed), and untreated (UTed) steel substrates on dissimilar laser aluminum (Al)/steel joints were comparatively investigated, for the first time, in terms of the interfacial microstructure and mechanical properties. Compared to the UTed joints, the interfacial microstructure of SMed joints remained unchanged with both composing of Fe-Al-Si and Fe-Al IMCs, but the joint fracture energy increased from 1.89 kJ to 2.39 kJ. Differently, the interfacial microstructure changed to a composite structure consisting of a high entropy alloys (HEAs) skeleton and reaction regions, and the joint fracture energy further increased to 4.38 kJ in the case of AMed joints. The mechanisms of the altered interfacial microstructure and tensile properties were also investigated.

Novel self-pretreatment of biomass by in-situ preparation of acid-assisted carbohydrate-derived DES

Deep eutectic solvents (DES) can greenly and efficiently fractionate biomass, but their utilization efficiency is severely limited by the high ratio of DES required and the wasted hemicelluloses released during the pretreatment. Herein, this work first developed a novel self-pretreatment of biomass by in-situ preparation of acid-assisted carbohydrate-derived DES with the aid of ball milling to facilitate enzymatic hydrolysis. The effect of hydrogen bond acceptor types, water content, acid content, and ball-milling time on enzymatic hydrolysis was studied systematically. Under the optimal condition (tetrabutylammonium chloride (TBAC), 1000 wt% H2O, 100 wt% acids, ball milling for 2 h), the yields of glucose and xylose produced from the pretreated substrates after enzymatic hydrolysis were >99.9 % and 88 %, respectively. Furthermore, the structural integrity of the residual lignin was well-preserved, making it suitable for positional structural characterization and ideal substrates for lignin degradation. Characterization suggested that the hemicelluloses fragments via in-situ acid hydrolysis acted as hydrogen bond donors and combined in situ with TBAC to form DES. This strategy avoided the use of high dosages of DES and the wastage of hemicelluloses, and promoted the sustainability of the entire biorefinery process.

Friction and wear characteristics of DLC-terminated coatings deposited on AlSi10Mg alloy produced by Additive Manufacturing

Al–Si alloys are attractive materials for the fabrication of mechanical components, mainly because of their high strength-to-density ratio. Though the advent of Selective Laser Melting (SLM) has potentially expanded the range of their applicability, their poor tribological performances limit their effective use. Identifying post-processing protocols and coating strategies enhancing these properties and compatible with large-scale production is fundamental to the industrial uptake of SLM-fabricated Al–Si parts. This work tests the possibility of depositing self-lubricating Diamond-Like Carbon (DLC)-terminated films on AlSi10Mg built by SLM and subjected to different surface finishing processes. The applied coating architectures consist of an electroless nickel‐phosphorus buffer layer deposited on the AlSi10Mg surface, plus a series of interlayers and a DLC top film grown by Plasma Assisted – Chemical Vapor Deposition. The wear resistance and frictional behavior of the samples are evaluated for different substrate pre-treatments and coating assemblies under two applied loads. Cast substrates, processed and coated in a similar way, are also studied for comparison. The DLC film lends good tribological performances to all the coating-substrate combinations explored, being mechanically assisted by the underlying Ni–P layer. The friction coefficients stabilize around 0.20 at the lowest load, independently of the sample surface roughness (Sq), which spans the range 0.47–4.6 μm. Conversely, the counterpart wear rates increase with roughness up to 10−5 mm3/(N⋅m). Both tribological parameters decrease by nearly 20 % and 70 %, respectively, after a tenfold increase in load. These results indicate that DLC-terminated multilayers are extremely efficient on AlSi10Mg even in the presence of significant roughness. Their application requires a limited number of well-established processing steps also in the case of SLM grown parts.

Engineering Triphasic Nanocomposite Coatings on Pretreated Mg Substrates for Biomedical Applications.

Biodegradable polymer-based nanocomposite coatings provide multiple advantages to modulate the corrosion resistance and cytocompatibility of magnesium (Mg) alloys for biomedical applications. Biodegradable poly(glycerol sebacate) (PGS) is a promising candidate used for medical implant applications. In this study, we synthesized a new PGS nanocomposite system consisting of hydroxyapatite (HA) and magnesium oxide (MgO) nanoparticles and developed a spray coating process to produce the PGS nanocomposite layer on pretreated Mg substrates, which improved the coating adhesion at the interface and their cytocompatibility with bone marrow derived mesenchymal stem cells (BMSCs). Prior to the spray coating process of polymer-based nanocomposites, the Mg substrates were pretreated in alkaline solutions to enhance the interfacial adhesion strength of the polymer-based nanocomposite coatings. The addition of HA and MgO nanoparticles (nHA and nMgO) to the PGS matrix, as well as the alkaline pretreatment of the Mg substrates, significantly enhanced the interfacial adhesion strength when compared with the PGS coating on the nontreated Mg control. The average BMSC adhesion densities were higher on the PGS/nHA/nMgO coated Mg than the noncoated Mg controls under direct contact conditions. Moreover, the addition of nHA and nMgO to the PGS matrix and coating the nanocomposite onto Mg substrates increased the average BMSC adhesion density when compared with the PGS/nHA/nMgO coated titanium (Ti) and PGS coated Mg controls under direct contact. Therefore, the spray coating process of PGS/nHA/nMgO nanocomposites on Mg substrates or other biodegradable metal substrates could provide a promising surface treatment strategy for biodegradable implant applications.

Enzymatic hydrolysis of highly concentrated substrates obtained from Miscanthus giganteus

This work is the first to study the enzymatic hydrolysis of four types of substrates obtained from Miscanthus giganteus of the KAMIS variety of Russian breeding. The study was conducting using the authors’ methodology based on a chemical pretreatment of substrates at atmospheric pressure with HNO3 and NaOH dilute solutions. A one-stage pretreatment of Miscanthus giganteus allows the polysaccharide content to be increased up to 90.4–90.8%, compared to 98.3–99.4% following a two-stage treatment. The experimental results of enzymatic hydrolysis of the four obtained substrates in the range of initial concentrations from 30 to 120 g/l are approximated using fractal kinetics approaches. An increase in the initial substrate concentrations in the specified range leads to an increase in the initial hydrolysis rate by 2.8–3.3 times and a decrease in the yield of reducing sugars by 12.4–13.1%. All four pretreatment types turned out to be extremely effective for Miscanthus giganteus, ensuring an increase in the reactivity to enzymatic hydrolysis by 34–36 times compared to the starting raw material. Lowered yields of reducing sugars are observed during enzymatic hydrolysis of the alkaline delignification product of Miscanthus giganteus, which is associated with the resistance of Miscanthus giganteus to treatment with sodium hydroxide. An increase in the initial concentration of substrates from 60 to 90 g/l does not lead to a significant decrease in the yield of reducing sugars. Therefore, enzymatic hydrolysis of highly concentrated substrates can be successfully used to produce biofuels and biochemicals.

A Comprehensive Review of Group-III Nitride Light-Emitting Diodes: From Millimeter to Micro-Nanometer Scales.

This review describes the development history of group-III nitride light-emitting diodes (LEDs) for over 30 years, which has achieved brilliant achievements and changed people's lifestyles. The development process of group-III nitride LEDs is the sum of challenges and solutions constantly encountered with shrinking size. Therefore, this paper uses these challenges and solutions as clues for review. It begins with reviewing the development of group-III nitride materials and substrates. On this basis, some key technological breakthroughs in the development of group-III nitride LEDs are reviewed, mainly including substrate pretreatment and p-type doping in material growth, the proposal of new device structures such as nano-LED and quantum dot (QD) LED, and the improvement in luminous efficiency, from the initial challenge of high-efficiency blue luminescence to current challenge of high-efficiency ultraviolet (UV) and red luminescence. Then, the development of micro-LEDs based on group-III nitride LEDs is reviewed in detail. As a new type of display device, micro-LED has drawn a great deal of attention and has become a research hotspot in the current international display area. Finally, based on micro-LEDs, the development trend of nano-LEDs is proposed, which is greener and energy-saving and is expected to become a new star in the future display field.

Enhancement of biogas production by means of ultrasonic pre-treatment: state of art and review

Currently, fossil fuels are being used in an aberrant manner and greenhouse gases are negatively impacting the environment, causing research into renewable energy sources to be pioneered. As highlighted during the COP conferences, the international community is striving to expedite worldwide climate action by reducing emissions, intensifying adaptation initiatives, and increasing the availability of suitable financial resources. Production of biogas is a way to help overcome these challenges by reducing wastage and preventing environmental damage. The anaerobic digestion technique faces some barriers like elongated reaction times, cost of heating or low biogas yields. Several techniques have been used to enhance the biogas yield. Among these techniques the use of ultrasound technology as a pretreatment in biogas production revolutionized the process with its widespread application, providing an environmentally friendly and low-cost alternative. This paper reviews several research studies on ultrasonic pretreatment of several substrates categorized according to different sources, for biogas production and puts an effort to compare and advise various operation parameters.

Assessment of the Impact of Pretreatment of Spent Coffee Grounds with Diluted Sulfuric Acid on the Efficiency of Methane and Lactic Acid Fermentation

Lignocellulosic materials are composed of three major biocomponents such as cellulose, hemicellulose and lignin, which form a compact lignocellulosic complex. Characterized by high caloric content, lignocellulosic biomass, including coffee grounds, is a valuable energy source that can be efficiently used in various bioconversion and biotransformation processes. Due to the high consumption of coffee in the world, there is an increasing amount of coffee grounds, which is a rich waste and at the same time a valuable secondary raw material, and its use fits perfectly into a closed-loop economy. Coffee grounds biomass contains polysaccharides, mainly mannans, proteins, lipids, polyphenols, which will allow the development of different biorefinery strategies, the creation of new value-added products with reduced waste generation. The research describes the pre-treatment of coffee grounds with dilute sulfuric acid to evaluate the effect of acid concentration, hydrolysis time on biogas yield, including methane and lactic acid biosynthesis during anaerobic fermentations. A yield of 381.12 mL of CH4/g-VS methane was obtained, accounting for 72.48% of the total biogas composition. It was found that the most efficient sample in terms of substrate pre-treatment for lactic acid biosynthesis was coffee grounds after 90 min hydrolysis with 1.5% H2SO4 at 121 °C.

A durable superhydrophobic surface with bud-particle structure prepared by one-step spray method

Superhydrophobic surfaces play an essential role in numerous applications such as anti-fouling, waterproofing, and drag reduction due to their water-repellent. However, for most fabrication methods, there are high requirements for the preparation process and conditions. Meanwhile, the superhydrophobic surfaces generally have the problem of insufficient durability. In this study, a one-step method to fabricate a stable superhydrophobic surface by spraying is proposed. A new bud-particle structure is obtained by modifying micron and nano Aluminium hydroxide(Al(OH)3) particles, which helps the coated surface to demonstrate excellent superhydrophobicity with the water contact angle ∼157.0° and rolling angle ∼2.0°, and it shows great repellency to water droplet impact. Due to the compatibility of Al(OH)3with the pretreatment substrate and the reinforcing effect of nanoparticles, the coating maintained the superhydrophobicity well in the sandpaper wear and the ultrasonic damage test, which reflects the outstanding robustness of the coating.Moreover,benefiting from the control of the wetting state by micronand nanoparticles doping,the coating showed an excellent underwater drag reduction effect in the rheometer experiment, with a drag reduction rate of ∼67.7 %. The one-step spraying method proposed is a simple and convenient way to create the surface with excellent superhydrophobicity and durability, which has great potential applications in improving metal surface oxidation resistance and underwater reducing drag.

Energy efficiency of hydrogen production during dark fermentation

It is widely known that most of the world's energy is produced from non-renewable energy sources such as crude oil and coal. Hydrogen is an ideal fuel candidate with a high energy content and clean combustion product. Biohydrogen is an environmentally friendly, renewable biofuel with high energy density, making it a viable alternative to fossil fuels in the future. At the same time, despite the large number of articles on the intensification of both dark fermentation and anaerobic bioconversion in general, the operating costs of the proposed intensification methods are not well covered in the literature. The goal of the work was to estimate the conversion coefficient of thermal and electrical energy spent on the functioning of the process of dark fermentation of various organic wastes into the energy of produced hydrogen. A block diagram of the energy flows of the dark fermentation system and the structure of the energy consumption of the system were developed. The obtained literature and experimental data suggest that the conversion coefficient of energy into biohydrogen in the process of dark fermentation is less than 1, so to obtain 1 kWh of hydrogen it is necessary to expend more than 1 kWh of energy. At the same time, the use of a vortex layer apparatus for dark fermentation of the food waste model made it possible to increase the energy output of the process by more than 7 times, thereby bringing the values of the conversion coefficients of thermal and electrical energy closer to 1. Despite the fact that the energy efficiency of most known methods for producing hydrogen is higher than the energy efficiency of dark fermentation, it is worth noting that the raw material for producing hydrogen in the dark fermentation process is organic waste, and not high-energy fuel (natural gas, methane, coal) or water in the case of electrolysis. In addition, the use of a vortex layer apparatus for pre-treatment of the dark fermentation substrate made it possible to achieve electricity conversion coefficient values 40% higher than with water electrolysis.

Saccharification of Different Delignified Sawdust Masses from Various Trees Along the Lagos Lagoon in Nigeria

Sawdust, a major waste product of the forestry industry, is accumulating along the Lagos Lagoon in Lagos, Nigeria, without it being effectively managed. Besides its use in The saccharification of sawdust could contribute to the development of renewable energy sources and feedstock for bioproduct development. The process is, however, not that straightforward as variables such as the type of cellulase enzyme, pretreatment of the cellulose substrate, and optimizing of cellulase to cellulose ratio are a few that need to be optimized for the process to be effective in terms of glucose production.manufacturing sound-absorbing boards to reinforce concrete beams and for energy purposes, its potential as a renewable energy source and feedstock for bio-product development has not yet been realized. Cellulose, a glucose biopolymer and structural component of cellulose can be hydrolyzed by a hydrolytic enzyme known as cellulase. During the process, the enzyme breaks the B-1,4-glucosidic bond, which keeps the glucose units together, and by acting on this bond, numerous glucose units are released. As part of sawdust, the cellulose molecule is not freely available for the degradation action of the cellulase enzyme as it is strongly associated with lignin, which acts as bio-glue, keeping cellulose and hemicellulose together. Delignification is an effective technique that was used to make the sawdust from ten different trees along the Lagos Lagoon in Nigeria more susceptible to saccharification by cellulase isolated from the fungus Aspergillus niger. Delignified and non-delignified sawdust masses between 2 mg and 10 mg were incubated with the A. niger cellulase solution (2 mg.mL-1), whereafter, the amount of sugar produced by the cellulase action was determined. The percentage saccharification of each sawdust material was also linked with the amount of sugar produced during cellulase action. From these investigations was concluded that delignification increased sugar production when almost all the masses of different sawdust materials were degraded. It was also observed that the ratio of sawdust mass to enzyme concentration is an important variable that influences the effectiveness of the saccharification process. The percentage saccharification of the various sawdust materials was also determined, and it indicated that the highest percentage of saccharification was not obtained when the highest amount of sawdust was degraded, producing the highest amount of sugar.

Integrated approach for co-production of bioethanol and light aromatics from lignocellulose through polyethylene glycol-aided acidic glycerol pretreatment

Acid-catalyzed glycerol organosolv (GO) pretreatment is a promising method for lignocellulosic biomass (LCB) fractionation. However, this method often leads to lignin repolymerization, intensifying lignin's inhibitory effects on subsequent enzymatic hydrolysis and limiting the production of highly active lignin, thereby hindering its valorization. This study explored incorporating polyethylene glycol (PEG) into acidic-catalyzed GO to improve bioethanol and bio-oil yields, with a focus on improving the yield of light aromatics, from LCB. Optimized PEG-aided GO pretreatment achieved a significantly higher bioethanol yield (23.7 g/L) compared to GO (17 g/L) and dilute acid (DA: 11.3 g/L) pretreatments. This improvement is attributed to the ability of PEG to mitigate lignin inhibition and modify the physicochemical properties of the pretreated substrate. Furthermore, thermal pyrolysis of PEG-aided GO lignin, obtained after the fermentation process, resulted in a substantially increased bio-oil yield (45.5 %) compared to GO (19 %) and DA (12 %). The enhanced bio-oil yield from PEG-aided GO lignin is ascribed to the promotion of β-O-4 linkages and the formation of β-O-4′ linkages. Characterization of the pyrolysis bio-oil revealed that light aromatic compounds were the dominant fraction, with their relative abundance significantly increasing from DA (5.9 %) to GO (9.7 %) and PEG-aided GO lignin (24.9 %). The PEG-aided GO method achieved an energy output of 8.85 MJ/kg, exceeding that of the GO and DA methods by 31 % and 57 %, respectively. The energy conversion efficiency of the PEG-aided GO method was 70 %, demonstrating a significant improvement compared to GO (57 %) and DA (51 %). This approach promotes the circular economy by upcycling LCB for bioethanol and valuable light aromatic compound production.

Novel approach to produce 3D boron-doped diamond for pollutant removal from water

Diamond growth from Chemical Vapor Deposition (CVD) on foreign substrates can require different pretreatment not only to improve the film nucleation but also to assure its adhesion by decreasing the expected film/substrate interface stress. To improve boron-doped film nucleation, growth, and adherence, different substrate pretreatments have been used mainly from the seeding process with diamond powder at various particle sizes. Despite this, the development of diamond growth on a Ti mesh remains difficult because of the requirement of a cohesive film to cover a 3D macroporous sample with varying growth rates based on its distinct network geometry. Then, this work describes a novel approach to growing boron-doped diamond (BDD) and boron-doped ultrananocrystalline diamond (B-UNCD) on titanium dioxide nanotubes (TDNT) produced simultaneously on both sides of Ti mesh by an anodization process. The films were obtained from two-step growth processes by assuring the entire diamond overlay on both TDNT/Ti mesh sides, including their outer/inner surfaces, as a 3D sample. TiO2 - TiC conversion has dominated the renucleation process, facilitating the nanometric scale control. The film morphologies were systematically analyzed by FEG-SEM images at different sample planes and depths for both sample sides at different stages of film growth. The unique morphology of titania nanotubes associated with columnar and/or renucleation development of BDD, considering the film defects and valley, can systematically increase the electrode specific area. Raman spectra showed the film quality and its micro and/or ultrananodiamond structure and the boron doping features. Also, this growth process allowed a dopant-controlled adjustable conductivity. Then, the boron doping levels for both films were evaluated from Mott-Schottky plots at around 1019 Bcm−3, characterizing them with good conductivity. In addition, electrochemical measurements from Cyclic Voltammetry (CV) confirmed the expected diamond response on redox pair following the quasi-reversible criteria as high-performance diamond electrodes and in situ Raman spectroelectrochemical measurements assessed the stability of samples during electrochemical measurements, ensuring structural integrity. Finally, the samples were applied to the degradation of methylene blue, proving to be superior materials for electrochemical applications due to their advantages compared to those of similar 2D electrodes.

Supercharged cellulases show superior thermal stability and enhanced activity towards pretreated biomass and cellulose

Non-productive binding of cellulolytic enzymes to various plant cell wall components, such as lignin and cellulose, necessitates high enzyme loadings to achieve efficient conversion of pretreated lignocellulosic biomass to fermentable sugars. Protein supercharging was previously employed as one of the strategies to reduce non-productive binding to biomass. However, various questions remain unanswered regarding the hydrolysis kinetics of supercharged enzymes towards pretreated biomass substrates and the role played by enzyme interactions with individual cell wall polymers such as cellulose and xylan. In this study, CBM2a (from Thermobifida fusca) fused with endocellulase Cel5A (from T. fusca) was used as the model wild-type enzyme and CBM2a was supercharged using Rosetta, to obtain eight variants with net charges spanning −14 to +6. These enzymes were recombinantly expressed in E. coli, purified from cell lysates, and their hydrolytic activities were tested against pretreated biomass substrates (AFEX and EA treated corn stover). Although the wild-type enzyme showed greater activity compared to both negatively and positively supercharged enzymes towards pretreated biomass, thermal denaturation assays identified two negatively supercharged constructs that perform better than the wild-type enzyme (∼3 to 4-fold difference in activity) upon thermal deactivation at higher temperatures. To better understand the causal factor of reduced supercharged enzyme activity towards AFEX corn stover, we performed hydrolysis assays on cellulose-I/xylan/pNPC, lignin inhibition assays, and thermal stability assays. Altogether, these assays showed that the negatively supercharged mutants were highly impacted by reduced activity towards xylan whereas the positively supercharged mutants showed dramatically reduced activity towards cellulose and xylan. It was identified that a combination of impaired cellulose binding and lower thermal stability was the cause of reduced hydrolytic activity of positively supercharged enzyme sub-group. Overall, this study demonstrated a systematic approach to investigate the behavior of supercharged enzymes and identified supercharged enzyme constructs that show superior activity at elevated temperatures. Future work will address the impact of parameters such as pH, salt concentration, and assay temperature on the hydrolytic activity and thermal stability of supercharged enzymes.

Nanoarchitectonics of bamboo-based heterojunction photocatalyst for effective removal of organic pollutants

A high-performance photocatalyst with both efficient and reusable performance is essentially demanded for the purification of organic wastewater and the removal of indoor formaldehyde. However, recovery of photocatalyst particles from the reaction system remains a challenge. Herein, based on the abundant pore structure of natural bamboo and the outstanding photocatalytic activity of ZnO/WO3, we fabricated an efficient bamboo-based photocatalyst (ZnO/WO3@bamboo) for the efficient photocatalytic degradation of formaldehyde and organic dyes. The pretreatment of bamboo substrates with NaOH solution resulted in the formation of nucleation sites for ZnO/WO3 growth within bamboo cellulose channels. Subsequently, the as-prepared ZnO and WO3 were mixed in different mass ratios, and loaded on the pretreated bamboo substrates using the hydrothermal method. The results showed that the ZnO/WO3@bamboo had the effective function of photocatalytic degradation of formaldehyde gas and organic dyes. Moreover, the as-prepared ZnO/WO3@bamboo photocatalyst demonstrated superior recycling ability toward organic pollutants, which was described by photocatalytic degradation efficiency of formaldehyde gas more than 89% after 10 cycles, and organic dyes over 93% after 20 cycles. The coupling of ZnO and WO3 leads to electron delocalization, which caused the electron holes generated in the valence band (VB) of ZnO to delocalize to the VB of WO3, and reduced the recombination of electron-hole. Therefore, the photocatalytic degradation performance of the ZnO/WO3@bamboo was enhanced. The proposed ZnO/WO3@bamboo photocatalyst holds great promise in the field of air pollution and wastewater remediation.

Anaerobic Two-Phase Co-Digestion for Renewable Energy Production: Estimating the Effect of Substrate Pretreatment, Hydraulic Retention Time and Participating Microbial Consortia

Green and sustainable economies have recently become a key issue in long-term growth and well-being. Co-digestion of various waste materials in an eco-friendly way through biogas production has become the preferred method for their utilization and valorization. The possibility of hydrogen and methane yield maximization depends on the most suitable alkali reagent for pretreatment of waste lignocellulosic material, which was revealed in batch tests to determine the hydrogen production potential. The mixture for digestion consisted of pretreated wheat straw mixed with waste algal biomass in a ratio of 80:20 (w/w). The maximum hydrogen yield was achieved after applying sodium hydroxide thermoalkaline pretreatment, with a two-fold higher yield than the untreated control. Hydrogen production was stable and methane was not present in the resultant gas. The influence of the hydraulic retention time (HRT) on the maintenance of cascade installation was studied. The maximum daily concentration of hydrogen was achieved at an HRT of 2 days—42.5% H2—and the maximum concentration of methane was 56.1% at an HRT of 6 days. Accumulation of volatile fatty acids was registered in the first step and their depletion was noted in the second one. The obtained values of the cellulose content demonstrated that it was utilized by up to 2.75% in the methanogenic bioreactor at the end of the process. Metagenomics analyses revealed the bacteria Thermocaproicibacter melissae (44.9%) and Clostridium cellulosi (41.9%) participated in the consortium, accomplishing substrate hydrolysis and acidogenesis in the first stage. Less in abundance were Thermoanaerobacterium butyriciformans, Calorimonas adulescens, Pseudomonas aeruginosa and Anaerocolumna chitinilytica. Methanogenesis was performed by an archaeon closely related to Bathyarchaeota (99.5%) and Methanobacterium formicicum. The most abundant bacterial strains in the methanogenic fermenter were Abyssalbus ytuae (30%), Proteiniphilum acetatigenes (26%) and Ruficoccus amylovorans (13%).

Unveiling a 72.5 GPa peak hardness in sustainable nanodiamond composite hard coatings via discharge energy control: A nanoindentation-Raman approach

Sustainable nanodiamond composite (NDC) films hold promise for high-performance hard coatings thanks to coaxial arc plasma deposition (CAPD). This eco-friendly technique eliminates the need for external heating, chemical reactions, or Co substrate pre-treatment. CAPD boasts lower energy consumption and faster deposition rates, making it a sustainable solution for the growing demand for high-quality, environmentally friendly coatings. This study investigates the influence of discharge energy on the nanostructure and mechanical properties of these NDC films. Optimal discharge energy, ranging from 2.3 to 12 J/pulse, was meticulously explored. A combined nanoindentation-Raman approach reveals a significant correlation between discharge energy and film properties. Remarkably, at 7 J/pulse, a peak hardness of 72.5 GPa is achieved, surpassing other energy levels. Raman spectroscopy confirms maximum nanodiamond content at this energy level (evidenced by maximized Adia/AG ratio, indicating a higher diamond-to-graphite ratio), along with minimal graphitization. Additionally, the presence of trans-polyacetylene (t-PA) peaks (denoted as At-PA) revealed the existence of maximum grain boundaries ratio (At-PA/AG), contributing to enhanced mechanical properties. Optimizing discharge energy tailors NDC film nanostructure, enhancing mechanical performance for advanced hard coatings.