Production Rate Research Articles

Ecological risk assessment of castor oil based waterborne polyurethane: Mechanism of anionic/cationic state selective toxicity to Eisenia fetida

Cationic and anionic castor oil-based waterborne polyurethanes (C-WPU/A and C-WPU/C) have great potential for development in agriculture. However, it is still unclear whether these polyurethanes are harmful or toxic to soil fauna. Based on multilevel toxicity endpoints and transcriptomics, we investigated the effects of C-WPU/A and C-WPU/C on earthworms (Eisenia fetida). The acute toxicity results showed that C-WPU/A was highly toxic to the earthworms, whereas C-WPU/C was nearly nontoxic. C-WPU/A significantly affected the body weight, burrowing ability and cocoon production rate of earthworms compared to C-WPU/C. After exposure to C-WPU/A, the results showed accumulation of reactive oxygen species (ROS), abnormal peroxidase activity, and increased malondialdehyde levels. Additionally, more serious histopathological damage was observed in earthworms, such as epidermal damage, vacuolization, longitudinal muscle disorganization, and shedding of intestinal epidermal cells. At the cellular level, C-WPU/A induced more severe lysosomal damage, DNA damage and apoptosis than C-WPU/A. C-WPU/A made more differentially expressed genes and considerably more enriched pathways at the transcriptional level than C-WPU/C. These pathways are largely involved in cell membrane signaling, detoxification, and apoptosis. These results provide an important reference for elucidating the selective toxicity mechanisms of C-WPU/A and C-WPU/C in earthworms.

Intensification of ex-situ biomethanation in a bubble column bioreactor by addition of colonized biochips

Biological methanation is a promising sustainable energy technology. To intensify ex-situ biomethanation, a 3-L bubble column reactor was operated continuously under thermophilic conditions, with and without colonized biochips. Studies in batch reactors showed biofilm formation on biochips, with an archaea:bacteria ratio of 5.7 compared to 3.2 in planktonic phase with Methanothermobacter being the dominant archaea. Using colonized biochips in the bubble column increased methane production rate (MPR) nearly threefold, achieving a steady MPR of 15.7 ± 0.5 NLCH4/Lr.d at 84.4 ± 0.9 % methane content. Gas retention time (GRT) was 0.3 h, with 97.4 % and 96.5 % conversion of H2 and CO2, respectively. Volatile fatty acid (VFA) production was under 40 mg/L per day, indicating dominant hydrogenotrophic methanogenic (HM) pathway. The results suggest biofilm formation significantly enhances MPR in ex-situ methanation reactors, advancing towards industrial application.

Quasi-homogeneous photoelectrochemical organic transformations for tunable products and 100% conversion ratio

Photoelectrochemical (PEC) organic transformation at the anode coupled with cathodic H2 generation is a potentially rewarding strategy for efficient solar energy utilization. Nevertheless, achieving the full conversion of organic substrates with exceptional product selectivity remains a formidable hurdle in the context of heterogeneous catalysis at the solid/liquid interface. Here, we put forward a quasi-homogeneous catalysis concept by using the reactive oxygen species (ROS), such as ·OH, H2O2 and SO4•−, as a charge transfer mediator instead of direct heterogeneous catalysis at the solid/liquid interface. In the context of glycerol oxidation, all ROS exhibited a preference for first-order reaction kinetics. These ROS, however, showcased distinct oxidation mechanisms, offering a range of advantages such as ∼ 100 % conversion ratios and the flexibility to tune the resulting products. Glycerol oxidative formic acid with Faradaic efficiency (FE) of 81.2 % was realized by the H2O2 and ·OH, while SO4•− was preferably for glycerol conversion to C3 products like glyceraldehyde and dihydroxyacetone with a total FE of about 80 %. Strikingly, the oxidative coupling of methane to ethanol was successfully achieved in our quasi-homogeneous system, yielding a remarkable production rate of 12.27 μmol h−1 and an impressive selectivity of 92.7 %. This study is anticipated to pave the way for novel approaches in steering solar-driven organic conversions by manipulating ROS to attain desired products and conversion ratios.

A clean hydrogen and electricity co-production system based on an integrated plant with small modular nuclear reactor

The present study aims to develop a novel configuration of hydrogen and electricity co-production based on a small modular nuclear reactor (SMR) by synergistically integrating the Vanadium Chloride thermochemical (V–Cl) and helium-closed Brayton cycles. For the V–Cl thermochemical cycle, a steady-state simulation model is developed for the first time in the Aspen Plus environment. The entire system is assessed thermodynamically by calculating the exergy destruction rate and exergy efficiency of major components employed in different subsections (nuclear power production, clean hydrogen production, supporting Rankine cycle, hydrogen compression, and storage) of the plant. Various parametric studies are conducted to identify the scope of improvement and evaluate suitable operating parameters that exhibit optimized system performance. It is found that a maximum H2 production rate is achieved when the VCl4 flow is 3.6 kmol/h. A specific hydrogen production rate of 9.63 g/kWh is achieved. The reduction reactor and Deacon reactors are responsible for the highest and lowest exergy destruction with a value of 155.46 kW and 37.60 kW accounting for 49 % and 11.86 % of the overall exergy destruction within the V–Cl cycle. The share of power production from the secondary Rankine cycle in the overall hydrogen compression train is 16.48 %. The parametric study results show that with an outlet helium pressure of 15 bar, the overall work output and electrical efficiency peaked with a value of 4.6 MW and 15.64 % respectively. The overall energy and exergy efficiencies of the proposed system are found to be 16.94 % and 21.42 % respectively.

Fire-resistant and mechanically-robust phosphorus-doped MoS2/epoxy composite as barrier of the thermal runaway propagation of lithium-ion batteries

Thermal runaway propagation (TRP) is an utmost safety issue in battery modules owing to its derivative accidents of fire or explosion. This study develops a novel flame-retardant epoxy resin (EP) board to prevent the battery TRP. The phosphorus doped MoS2 nanowires (PR-MoS2) is designed and incorporated into EP matrix to acquire EP/3.0 PR-MoS2 composite. The composite shows 159.4 % increase in char yield, 56.7 % decrease in peak heat release rate, 56.6 % reduction in peak CO production rate. By using EP/PR-MoS2-3 (EP/3.0 PR-MoS2 composite with thickness of 3 mm) between 103450-pouch cells, TRP can be effectively stopped. Meanwhile, the temperature of surviving battery remains below 100 °C. Of note, the minimum changes in internal crystal structure, chemical composition and electrochemical characteristics are discerned for the surviving battery. This research will offer inspirations for the design of TRP suppression materials, guaranteeing the safety the battery.

Polychloride and benzene ring synergistically boosting photocatalytic degradation and nitrogen fixation performances of carbon nitride

The limited active site exposure, insufficient light absorption and poor charge behavior of carbon nitride (CN) limit its application in environmental remediation and clean energy production. In this study, ultrathin porous CN with enhanced photocatalytic activity was constructed by doping 2,2′,5,5′-Tetrachlorobenzidine (TB) into CN framework. The synergistic effect of polychloride and benzene rings on CN leads to the significant enhancement of range/intensity of visible-light harvest and charge behavior, as well as specific surface area. The optimal sample achieves 100% tetracycline photodegradation efficiency with a rate constant approximately 9 times of pristine CN, and total organic carbon removal efficiency reaches 78.2%. Moreover, photocatalytic ammonia production rate is 7 times of pristine CN. Through active species trapping experiments, ESR, LC-MS, toxicity prediction and DFT calculations, the main active species, degradation pathway, intermediates toxicity and enhanced mechanism of photocatalytic activity are investigated. This work provides a reference for simultaneously regulating the morphology, light absorption and charge behavior of CN-based photocatalyst for addressing environmental and energy concerns.

Hollow porous silica nanoreactors encapsulating VOx-decorated Pt nanoparticles for the reverse water–gas shift reaction

Reverse water–gas shift (RWGS) reaction is a desirable strategy for achieving CO2 utilization and enhancing CO production. Due to the endothermic nature and the chemical equilibrium of this reaction, the reaction is typically conducted at high temperatures (300 ∼ 1000 °C); however, high temperature conditions lead to the sintering of the catalyst, resulting in a catalyst deactivation. Herein we report the synthesis of a metal oxide (V or Mo oxide)-decorated Pt nanoparticles encapsulated in hollow porous silica nanoreactors (HPSNs) by a W/O micro-emulsion system using branched poly(ethyleneimine) (PEI) as a sacrificial metal–ligand. The HPSNs encapsulating VOx-decorated Pt nanoparticles (Pt-VOx@HPSNs) afforded a 1.8-fold increased activity in RWGS reaction at 500 °C compared with Pt@HPSNs with a net CO production rate of 1140.3 mmol/gcat/h and with nearly 100 % CO selectivity. In situ XAFS measurement and reaction kinetic analysis reveal that the interplay of Pt nanoparticles and the decorated V oxide, which simultaneously activate H2 and CO2, respectively, leads to a lowering of the activation energy and a faster CO production rate. Furthermore, the Pt-VOx@HPSNs catalyst retains over 92 % activity after 50 h of continuous operation at 500 °C with the aid of a protective silica shell. This work offers a strategy for the design and development of an efficient and stable heterogeneous catalyst for RWGS reactions.

Engineering of g-C3N4 for Photocatalytic Hydrogen Production: A Review.

Graphitic carbon nitride (g-C3N4)-based photocatalysts have garnered significant interest as a promising photocatalyst for hydrogen generation under visible light, to address energy and environmental challenges owing to their favorable electronic structure, affordability, and stability. In spite of that, issues such as high charge carrier recombination rates and low quantum efficiency impede its broader application. To overcome these limitations, structural and morphological modification of the g-C3N4-based photocatalysts is a novel frontline to improve the photocatalytic performance. Therefore, we briefly summarize the current preparation methods of g-C3N4. Importantly, this review highlights recent advancements in crafting high-performance g-C3N4-based photocatalysts, focusing on strategies like elemental doping, nanostructure design, bandgap engineering, and heterostructure construction. Notably, sophisticated doping techniques have propelled hydrogen production rates to a 104-fold increase. Ingenious nanostructure designs have expanded the surface area by a factor of 26, concurrently extending the fluorescence lifetime of charge carriers by 50%. Moreover, the strategic assembly of heterojunctions has not only elevated charge carrier separation efficiency but also preserved formidable redox properties, culminating in a dramatic hundredfold surge in hydrogen generation performance. This work provides a reliable and brief overview of the controlled modification engineering of g-C3N4-based photocatalyst systems, paving the way for more efficient hydrogen production.

Light-induced H2 generation in a photosystem I-O2-tolerant [FeFe] hydrogenase nanoconstruct

The fusion of hydrogenases and photosynthetic reaction centers (RCs) has proven to be a promising strategy for the production of sustainable biofuels. Type I (iron-sulfur-containing) RCs, acting as photosensitizers, are capable of promoting electrons to a redox state that can be exploited by hydrogenases for the reduction of protons to dihydrogen (H2). While both [FeFe] and [NiFe] hydrogenases have been used successfully, they tend to be limited due to either O2 sensitivity, binding specificity, or H2 production rates. In this study, we fuse a peripheral (stromal) subunit of Photosystem I (PS I), PsaE, to an O2-tolerant [FeFe] hydrogenase from Clostridium beijerinckii using a flexible [GGS]4 linker group (CbHydA1-PsaE). We demonstrate that the CbHydA1 chimera can be synthetically activated in vitro to show bidirectional activity and that it can be quantitatively bound to a PS I variant lacking the PsaE subunit. When illuminated in an anaerobic environment, the nanoconstruct generates H2 at a rate of 84.9 ± 3.1 µmol H2 mgchl-1 h-1. Further, when prepared and illuminated in the presence of O2, the nanoconstruct retains the ability to generate H2, though at a diminished rate of 2.2 ± 0.5 µmol H2 mgchl-1 h-1. This demonstrates not only that PsaE is a promising scaffold for PS I-based nanoconstructs, but the use of an O2-tolerant [FeFe] hydrogenase opens the possibility for an in vivo H2 generating system that can function in the presence of O2.

Cu-doped ZnCdS-based photocatalyst for efficient photocatalytic hydrogen production by photothermal assistance

In solar energy utilization, photocatalytic hydrogen production has been widely researched. To address issues such as low efficiency of photocatalysts, Cu-doped Zn0.5Cd0.5S composite photocatalysts were prepared using a hydrothermal method for photocatalytic hydrogen production. The Cu/Zn0.5Cd0.5S photocatalyst was characterized using XRD, XPS, SEM, TEM, UV–vis-DRS, fluorescence spectrophotometer, and electrochemical workstation. The results indicate that Cu doping alters the crystal and band structures of Zn0.5Cd0.5S. Hydrogen production experiments were conducted under xenon lamp irradiation, and at 45 °C, the highest hydrogen production rate was 2.72 and 1.63 times that of single Zn0.5Cd0.5S and Cu-doped Zn0.5Cd0.5S at room temperature (25 °C), respectively. Cu doping imparted a photothermal effect to the photocatalytic hydrogen production experiment, enhancing its efficiency.Cu doping captured electrons by replacing some Zn, constructing an internal electric field, forming defect energy levels, which hindered electron-hole recombination. Additionally, Cu ions acted as a plasma, inducing a plasma effect during hydrogen production, accelerating the rate of solar energy conversion to thermal energy, thus improving hydrogen production efficiency. This research not only provides a photocatalyst for photocatalytic hydrogen production but also utilizes it for photothermal synergistic catalysis.

Mitigating Intraphase Catalytic-Domain Transfer via CO2 Laser for Enhanced Nitrate-to-Ammonia Electroconversion and Zn-Nitrate Battery Behavior.

Developing sustainable energy solutions is critical for addressing the dual challenges of energy demand and environmental impact. In this study, a zinc-nitrate (Zn-NO3-) battery system was designed for the simultaneous production of ammonia (NH3) via the electrocatalytic NO3- reduction reaction (NO3RR) and electricity generation. Continuous wave CO2laser irradiation yielded precisely controlled CoFe2O4@nitrogen-doped carbon (CoFe2O4@NC) hollow nanocubes from CoFe Prussian blue analogs (CoFe-PBA) as the integral electrocatalyst for NO3RR in 1.0-M KOH, achieving a remarkable NH3 production rate of 10.9 mgh-1cm-2 at -0.47 V versus RHE with exceptional stability. In-situ and ex-situ methods revealed that the CoFe2O4@NC surface transformed into high-valent Fe/CoOOH active-species, optimizing the adsorption energy of NO3RR (*NO2 and *NO species) intermediates. Furthermore, DFT calculations validated the possible NO3RR pathway on CoFe2O4@NC starting with NO3- conversion to *NO2 intermediates, followed by reduction to *NO. Subsequent protonation forms the *NH and *NH2 species, leading to NH3 formation via final protonation. The Zn-NO3- battery utilizing the CoFe2O4@NC cathode exhibits dual functionality by generating electricity with a stable open-circuit voltage of 1.38-V versus Zn/Zn2+ and producing NH3. This study inspires the simple design of low-cost catalysts for NO3RR-to-NH3 conversion and positions the Zn-NO3- battery as a promising technology for industrial applications.

Improved Nitrate‐to‐Ammonia Electrocatalysis through Hydrogen Poisoning Effects

Improved Nitrate‐to‐Ammonia Electrocatalysis through Hydrogen Poisoning Effects

Synergistic strategy of Z-scheme heterojunction and defect engineering to construct ZnS/CoSx nanospheres for excellent photocatalytic H2 evolution performance

The design of Z-scheme heterojunction to realize the efficient separation of charge carriers still remain challenging. Herein, the defect-assisted Z-scheme heterojunction strategy has been proposed. The binary ZnS/CoSx nanospheres were successfully prepared via a well-designed hydrothermal approach. The resultant ZnS/CoSx nanospheres with CoSx content of 5 wt% exhibit the optimal hydrogen production rate of 2546.6 μmol g−1h−1, which is 2.6 times higher than that of pure ZnS and superior to the most reported ZnS-based composites. The enhancement of S-vacancy concentration can greatly strengthen photocatalytic hydrogen evolution property, which can be originated from the boosted direct Z-scheme charge-transfer process in ZnS/CoSx heterostructures. The synergistic effect of direct Z-scheme heterostructures and defects engineering notably enhances the photocatalytic activity of ZnS/CoSx nanospheres, which could provide a deep insight for the design and synthesis of new types of photocatalysts.

Self-assembled chromium-based nitrogen carrier for chemical looping ammonia synthesis

Industrially, ammonia is generated mainly using the energy-intensive and CO2-emitting Haber-Bosch process, which is not conducive to sustainable economic and social development. The chemical looping ammonia synthesis (CLAS) is capable of coupling green energy, which is one of the available alternatives to the Haber-Bosch process, but the ammonia production rate of most of its nitrogen carriers is unsatisfactory. In this work, we designed a self-assembled nitrogen carrier using ZSM-5 molecular sieve (ZSM-5) and nickel (Ni) to modify chromium nitride (CrN). ZSM-5 molecular sieves have a rich pore structure, which enables the gas-phase reactants to react with the lattice nitrogen in the subsurface layer of the nitrogen carrier. Nickel can facilitate the dissociation of hydrogen during hydrogenation due to its higher hydrogen affinity. The ammonia production rate of the nitrogen carrier can reach 451.2 μmol g−1 h−1 at 700 °C and atmospheric pressure, and be able to remain 358 μmol g−1 h−1 after eight cycles. Furthermore, we also propose a full-coverage design strategy for nitrogen carriers: simultaneous optimization of the chemical and mass transfer processes in the nitrogen carrier. This work advances the design of high-performance nitrogen carrier, thus facilitating the applications of CLAS for the distributed ammonia synthesis.

Using Extracted Sugars from Spoiled Date Fruits as a Sustainable Feedstock for Ethanol Production by New Yeast Isolates.

This study focuses on investigating sugar recovery from spoiled date fruits (SDF) for sustainable ethanol production using newly isolated yeasts. Upon their isolation from different food products, yeast strains were identified through PCR amplification of the D1/D2 region and subsequent comparison with the GenBank database, confirming isolates KKU30, KKU32, and KKU33 as Saccharomyces cerevisiae; KKU21 as Zygosaccharomyces rouxii; and KKU35m as Meyerozyma guilliermondii. Optimization of sugar extraction from SDF pulp employed response surface methodology (RSM), varying solid loading (20-40%), temperature (20-40 °C), and extraction time (10-30 min). Linear models for sugar concentration (R1) and extraction efficiency (R2) showed relatively high R2 values, indicating a good model fit. Statistical analysis revealed significant effects of temperature and extraction time on extraction efficiency. The results of batch ethanol production from SDF extracts using mono-cultures indicated varying consumption rates of sugars, biomass production, and ethanol yields among strains. Notably, S. cerevisiae strains exhibited rapid sugar consumption and high ethanol productivity, outperforming Z. rouxii and M. guilliermondii, and they were selected for scaling up the process at fed-batch mode in a co-culture. Co-cultivation resulted in complete sugar consumption and higher ethanol yields compared to mono-cultures, whereas the ethanol titer reached 46.8 ± 0.2 g/L.

Investigation of the Effects of Ion Sources and RF Power on the Neutron Production Rate at SNRTC-IEC Fusion Device

Studies on an inertial electrostatic confinement (IEC) device are generally focused on increasing particle production. One way to achieve this is to increase the number of ion sources. In this study, the deuterium-deuterium fusion reaction was carried out in the IEC Saraykoy Nuclear Research and Training Center (SNRTC-IEC) fusion device (previously at the Turkish Atomic Energy Authority, now reestablished as the Turkish Energy, Nuclear and Mineral Research Agency) at cathode voltage of 85 kV and pressure of 5 × 10−4 mbars, and the effect of ion sources and radio-frequency (RF) power on the neutron production rate was investigated. To ensure a high concentration of ions in the center of the cathode, three inductively coupled plasma deuterium ion sources were added to this device. As the number of ion sources increased from one to three, the neutron production rate increased from 2.3 × 104 to 3.6 × 105n/s. Two ion source configurations were used to examine the effect of RF power. It was observed that when the RF power was increased from 40 to 200 W, the neutron production rate increased linearly from 4.6 × 104 to 1.7 × 105 n/s.

Microenvironment design strategies for enhanced CO2 electroreduction with a 60% full-cell energy efficiency

Low current densities (production rates) and low energy efficiency (EE) caused by poor catalyst activities and limited CO2 mass transfer in the catalyst layer (CL) prevent CO2 electrolysis from application. Herein, we report atomically dispersed Ni catalysts anchored on macroporous hollow nano-carbon sheets (A-Ni@CS) that simultaneously optimizes the coordination of Ni atoms and CO2 transport in the CL. The unique Ni–N5–O/C structure of A-Ni@CS lowers the energy barrier of *COOH formation, and the layered nano-to-micro porous structure increases the mass transfer of CO2, enhancing the local CO2 concentration in the CL. By employing a zero-gap flow cell, A-Ni@CS can mediate CO2 to CO conversion with a 60 % full-cell EE at 200 mA/cm2.

Functional and metabolic effects of omega-3 polyunsaturated fatty acid supplementation and the role of β-hydroxy-β-methylbutyrate addition in chronic obstructive pulmonary disease: A randomized clinical trial

IntroductionShort-term (4 weeks) supplementation with n-3 polyunsaturated fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) has recently been shown to improve protein metabolism in a dose dependent way in normal weight patients with Chronic Obstructive Pulmonary Disease (COPD). Furthermore, EPA/DHA supplementation was able to increase extremity lean soft tissue but not muscle function. No studies are available combining n-3 PUFAs and the leucine metabolite β-hydroxy-β-methylbutyrate (HMB) supplementation in chronic clinical conditions. Whether adding HMB to daily EPA/DHA supplementation for 10 weeks enhances muscle and brain health, daily functional performance, and quality of life of patients with COPD by further improving their protein and amino acid homeostasis remains unknown. MethodsPatients with COPD (GOLD: II-IV, n=46) received daily for 10 weeks, according to a randomized double-blind placebo-controlled three-group design, EPA/DHA (n=16), EPA/DHA to which HMB was added (n=14), or placebo (n=16). The daily dose of 2.0 g of EPA/DHA or soy + corn oil as the placebo was provided via gel capsules, and 3.0 g of Ca-HMB or maltodextrin as placebo as powders. At pre- and post-intervention, a pulse mixture of multiple amino acids was administered to measure postabsorptive net protein breakdown (netPB as primary endpoint) and whole body production (WBP) and conversion rates of the amino acids. As secondary endpoints, lean soft tissue, and fat mass were assessed by dual-energy X-ray absorptiometry, upper and lower muscle function by handgrip and single leg isokinetic dynamometry, brain (cognitive, wellbeing) health by assessments, daily functional performance by measuring 6-minute walk distance, 4-meter gait speed, and postural balance, and quality of life by questionnaire. Plasma enrichments and concentrations were analyzed by LC-MS/MS, and systemic inflammatory profile and metabolic hormones by Luminex. ResultsHMB + EPA/DHA but not EPA/DHA supplementation increased postabsorptive netPB (p=0.028), and WBPs of glutamine (p=0.024), taurine (p=0.039), and tyrosine (p=0.036). Both EPA/DHA and HMB + EPA/DHA supplementation resulted in increased WBP of phenylalanine (p<0.05). EPA/DHA but not HMB + EPA/DHA was able to increase WBP of arginine (p=0.030), citrulline (p=0.008), valine (p=0.038), and conversion of citrulline to arginine (p=0.009). Whole body and extremity fat mass were reduced after HMB + EPA/DHA supplementation only, whereas lean soft tissue was increased after EPA/DHA (p=0.049) and HMB + EPA/DHA (p=0.073). No other significant findings were observed. Reductions in several proinflammatory cytokines were observed in the HMB + EPA/DHA group including IL-2, IL-17, IL-6, IL-1 receptor antagonist, IL-12P40, and TNF-β (p<0.05). ConclusionsTen weeks of supplementation with 2 g of EPA/DHA daily is sufficient to induce muscle gain in COPD but HMB is needed to induce fat loss. Whether HMB is solely responsible for the fat mass loss or has a synergistic effect with EPA/DHA remains unclear. The increase in net protein breakdown observed with HMB + EPA/DHA supplementation may not indicate harmful muscle catabolism but rather a beneficial enhanced protein turnover cycling associated with increased lean soft tissue. Clinical Trial RegistryClinicalTrials.gov; NCT03796455

Enhancing methane production from corn straw via illumination-assisted Fe3O4/g-C3N4 nanocomposite in anaerobic digestion

This study proposes a novel anaerobic digestion (AD) strategy combining recyclable photoactivated nanomaterials with illumination to enhance electronic transfer for anaerobic microorganisms. Results showed that 7000 Lux illumination increased methane production yield and rate. Incorporating Fe3O4 into graphite carbon nitride (g-C3N4) created a recyclable Fe3O4/g-C3N4 (FG) nanocomposite with improved light absorption, conductivity, redox properties, and methane promotion. The highest methane yield from corn straw was achieved with 7000 Lux and 1.5 g/L FG nanocomposite, 22.6% higher than the dark control. The AD system exhibited increased adenosine triphosphate content, improved redox performance, reduced electron transfer resistance, and higher photocurrent intensity. These improvements bolstered the microorganisms and key genes involved in hydrolysis and acidification, which in turn optimized the acetoclastic pathway. Furthermore, this strategy promoted microorganisms associated with direct interspecies electron transfer, fostering a favorable environment for methanogenic activities, paving the way for future anaerobic reactor developments.

Measurement dynamics and data treatment in fire testing

Fire testing is and will remain of paramount importance in helping industry, regulators and all other fire safety stakeholders to achieve a safer world. For this to happen, test data must be stable and reliable, regardless of the test facility that produced the data, its various operators, the measurement equipment used, and so on. The instruments and sensors used to measure heat release, smoke production and mass loss rate are susceptible to mechanical and/or electrical disturbances and all have their own dynamic behaviour. This leads to a variation in the test results. A scatter that is only due to the measurement.This paper examines the time and frequency domain behaviour of various measurement components and hardware & software filters in use today. It proposes an instrument-independent method of eliminating noise and other interference, describes a method of adjusting the response time of the various input signals to a common value applicable to all test institutes, and proposes a method of accurately synchronising these signals in time.The result is unambiguous qualitative measurement data that can be confidently compared with data from other sample sets or between different laboratories and researchers. It improves the stability and reproducibility of test results leading to a more stable classification of materials.