Degradation Rate Research Articles

Selective phthalate removal by molecularly imprinted biomass carbon modified electro-Fenton cathode

A novel molecularly imprinted biomass carbon (MIP@BC) catalyst functionalized with the virtual template of phthalates was designed as the cathode material which possesses excellent 2-electron oxygen reduction ability and H2O2 production capacity, which is suitable for targeted degradation of phthalates in the electro-Fenton system. Following molecularly imprinted modification, the adsorption capacity of MIP@BC for Dimethyl phthalate (DMP) increased by 40 %, reached 9.26 mg/g. Compared with non-imprinted biomass carbon (NIP@BC), the MIP@BC-mediated electro-Fenton process enhanced the degradation rate of DMP by 72 %. Additionally, the degradation rate of DMP rises by 51 % and 104 % respectively on the basis of river water and domestic sewage. The reactive oxygen species that induced DMP degradation were OH and O2− and targeted adsorption and catalysis exert a synergistic effect. This study provides a new insight into targeted degradation for high-toxicity of emerging contaminants from complex aqueous environment.

Recent replenishment of aliphatic organics on Ceres from a large subsurface reservoir.

Ceres hosts notable aliphatic-organic concentrations, ranging from approximately 5 to >30 weight % in specific surface areas. The origins and persistence of these organics are under debate due to the intense aliphatic organic signature and radiation levels in Ceres' orbit, which would typically lead to their destruction, hindering detection. To investigate this, we conducted laboratory experiments to replicate how the signature of the organic-rich regions would degrade due to radiation. Our findings indicate a fast degradation rate, implying the exposure of buried organics within the past few million years. This degradation rate, coupled with observed quantities, implies that the aliphatics must be present in substantial quantities within the shallow subsurface. Our estimates suggest an initial aliphatic abundance 2 to 30 times greater than currently observed, surpassing significantly the levels found in carbonaceous chondrites, indicating either a significant concentration or remarkable purity.

Zinc and chitosan-enhanced β-tricalcium phosphate from calcined fetal bovine bone for mandible reconstruction.

Mandibular defects pose significant challenges in reconstructive surgery, and scaffold materials are increasingly recognized for their potential to address these challenges. Among various scaffold materials, Beta-tricalcium phosphate (β-TCP) is noted for its exceptional osteogenic properties. However, improvements in its biodegradation rate and mechanical strength are essential for optimal performance. In this study, we developed a novel β-TCP-based scaffold, CFBB, by calcining fetal bovine cancellous bone. To enhance its properties, we modified CFBB with Chitosan (CS) and Zinc (Zn), creating three additional scaffold materials: CFBB/CS, CFBB/Zn2+, and CFBB/Zn2+/CS. We conducted comprehensive assessments of their physicochemical and morphological properties, degradation rates, biocompatibility, osteogenic ability, new bone formation, and neovascularization both in vitro and in vivo. Our findings revealed that all four materials were biocompatible and safe for use. The modifications with CS and Zn2+ significantly improved the mechanical strength, osteogenic, and angiogenic properties of CFBB, while concurrently decelerating its resorption rate. Among the tested materials, CFBB/Zn2+/CS demonstrated superior performance in promoting bone regeneration and vascularization, making it a particularly promising candidate for mandibular reconstruction. The CFBB/Zn2+/CS scaffold material, with its enhanced mechanical, osteogenic, and angiogenic properties, and a controlled resorption rate, emerges as a highly effective alternative for the repair of oral mandible defects. This study underscores the potential of combining multiple bioactive agents in scaffold materials to improve their functionality for specific clinical applications in bone tissue engineering.

Polyglycerol Sebacate/polycaprolactone/reduced graphene oxide composite scaffold for myocardial tissue engineering

The aim of this research was to fabricate and evaluate polyglycerol sebacate/polycaprolactone/reduced graphene oxide (PGS-PCL-RGO) composite scaffolds for myocardial tissue engineering. Polyglycerol sebacate polymer was synthesized using glycerol and sebacic acid prepolymers, confirmed by Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). Six PGS-PCL-RGO composite scaffolds (S1-S6) with various weight ratios were prepared in chloroform (CF) and acetone (Ace) solvents at 8 CF:2Ace and 9 CF:1Ace volume ratios, using the electrospinning method at a rate of 1 ml/h and a voltage of 18 kV. The scaffolds' chemical composition and microstructure were characterized by FTIR, XRD, and scanning electron microscopy (SEM). Further investigations included tensile testing, contact angle testing, four-point probe testing for electrical conductivity, degradation testing, and cytotoxicity testing (MTT). The results showed that adding 2%wt RGO to the composite scaffold decreased fiber diameter and degradation rate, while increasing electrical conductivity and ductility. The 33%PGS-65%PCL-2%RGO (S3) composite scaffold exhibited the lowest degradation rate (23.87 % over 60 days) and the highest electrical conductivity (51E-3 S/m). Mechanical evaluations revealed an elastic modulus of 2.46 MPa and elongation of 62.43 %, aligning closely with the heart muscle's elastomeric properties. The contact angle test indicated that the scaffold was hydrophilic, with a water contact angle of 61 ± 2°. Additionally, the cell toxicity test confirmed that scaffolds containing RGO were non-toxic and supported good cell viability. In conclusion, the 33%PGS-65%PCL-2%RGO composite scaffold exhibits mechanical and structural properties similar to heart tissue, making it an ideal candidate for myocardial tissue engineering.

A platinum degradation reaction model for the high-speed computation in the integrated fuel cell system simulator and its validation by the accelerated stress test data of the commercial fuel cells

A model to estimate the Pt degradation rate and the numerical methods for high-speed computation were developed for the year-long and system-scale durability simulation in an acceptable accuracy and computational time. The parameters in the model were determined to reproduce the published accelerated stress test (AST) data with the 1 cm2 MEA of 2nd-generation MIRAI (MIRAI-2), state-of-the-art commercial fuel cell electric vehicle. Accuracy of the simulation results was validated by the published data of the ASTs with the FC stack having 13 cells of MIRAI-2, which consists of the 30000 startup-shutdown cycles in 0–0.88 V and 73000 acceleration-deceleration cycles in 0.6–0.9 V. The experimental and simulation results of the residual fractions of the electrochemical surface area in the cathode catalyst layer after the ASTs were 68 and 69 %, respectively, and they agreed in an acceptable accuracy. It was confirmed from the AST simulation with the different initial particle size distributions that even the small number of the coarse particles significantly accelerated the Pt degradation. The developed model was integrated to the FC system simulator the current authors had presented and a remarkable computational speed for the year-long and system-scale durability simulation was demonstrated with a normal laptop computer.

A platinum degradation reaction model for the high-speed computation in the integrated fuel cell system simulator and its validation by the accelerated stress test data of the commercial fuel cells

A model to estimate the Pt degradation rate and the numerical methods for high-speed computation were developed for the year-long and system-scale durability simulation in an acceptable accuracy and computational time. The parameters in the model were determined to reproduce the published accelerated stress test (AST) data with the 1 cm2 MEA of 2nd-generation MIRAI (MIRAI-2), state-of-the-art commercial fuel cell electric vehicle. Accuracy of the simulation results was validated by the published data of the ASTs with the FC stack having 13 cells of MIRAI-2, which consists of the 30000 startup-shutdown cycles in 0–0.88 V and 73000 acceleration-deceleration cycles in 0.6–0.9 V. The experimental and simulation results of the residual fractions of the electrochemical surface area in the cathode catalyst layer after the ASTs were 68 and 69 %, respectively, and they agreed in an acceptable accuracy. It was confirmed from the AST simulation with the different initial particle size distributions that even the small number of the coarse particles significantly accelerated the Pt degradation. The developed model was integrated to the FC system simulator the current authors had presented and a remarkable computational speed for the year-long and system-scale durability simulation was demonstrated with a normal laptop computer.

Chemofunctionalization of knitted silk to improve interface connection in a nano/micro scaffold based on polycaprolactone-chitosan-multi-walled carbon nanotube/silk.

Nano/micro hybrid scaffolds in long-term healing tissue engineering can simultaneously offer both mechanical and biological properties. In this study, a hybrid scaffold was fabricated through electrospinning of polycaprolactone (PCL)-chitosan (Cs)/ multi-walled carbon nanotubes (MWCNTs) based nanofibers onto a chemically functionalized knitted silk substrate (F-Silk) and the scaffold were evaluated with regard to morphology, chemical and crystalline structure, hydrophilicity, mechanical properties, bioactivity, biodegradability, and cellular behavior. Chemical functionalization of silk using N-hydroxysuccinimide (NHS) and 1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) resulted in greater integrity in the formation of nanofibers onto the microfibers. The presence of MWCNTs significantly reduced the contact angle of the scaffolds from 79.72°±2.72 to 68.92°±5.63. Chemical functionalization of silk, the presence of nanofiber coating, and the presence of MWCNTs increased the ultimate tensile strength of the hybrid scaffolds by 18%, 20%, and 30% compared to raw silk fabric, respectively. The presence of MWCNTs and chemical functionalization of knitted silk increased the bioactivity and reduced the degradation rate of hybrid scaffolds. The increase in the amount of carboxyl groups as a result of adding 0.5wt% of MWCNTs significantly improved the adhesion, growth and proliferation of chondrocyte cells on the hybrid scaffolds as observed through cell morphology. According to the obtained results, hybrid scaffold based on PCL-Cs-MWCNTs/F-silk can be a suitable option for further research in cartilage tissue engineering.

Exploring the formation of S-scheme heterojunctions in CuFe2O4/Bi2MoO6 porous cubes for photocatalytic removal of tetracycline

Exploring highly active and noble metal-free photocatalysts for the efficient photocatalytic degradation of antibiotics is of great significance. The CuFe2O4 nanostructured cube is synthesized by using a self-sacrificial template strategy, and two-dimensional Bi2MoO6 nanosheets are grown on the surface of CuFe2O4 through a solvothermal method to construct CuFe2O4/Bi2MoO6 S-scheme heterostructure. The CuFe2O4/Bi2MoO6 composite material exhibits eminent photocatalytic activity for the degradation of TC under simulated sunlight, with the optimal ratio CFO/BMO-2 achieving a degradation rate of 98.54 % within 30 min (initial concentration of TC: 50 mg L−1). In addition, CFO/BMO-2 also has excellent magnetic recyclability and cycling ability. Rice cultivation tests demonstrate that the biotoxicity of TC is effectively removed. Density functional theory calculations and in-situ irradiated X-ray spectroscopy deeply reveal the mechanisms of charge separation and transfer of S-scheme heterojunctions in CuFe2O4/Bi2MoO6. The construction of S-scheme heterojunctions promotes the separation of photo-induced charge carriers and improves photocatalytic degradation performance by retaining holes and electrons with strong redox ability. The work provides a practicable method for constructing efficient spinel photocatalysts to drive wastewater treatment reactions, and the constructed magnetically recyclable photocatalysts have certain practical application potential.

Preparation and release pattern study of long-term controlled release Blonanserin microspheres

To prepare a PLGA microsphere loaded with the antipsychotic Blonanserin without release leg period and released in a near-zero model for long time, in this study, 15 kDa and 75 kDa PLGA were chosen to be mixed with different ratios, and Blonanserin microspheres (Bn-MS) without significant differences in the particle size, drug loading capacity, and encapsulation rate were prepared by microfluidics. The release kinetic model was fitted to the release behavior by monitoring the changes in particle size and morphology during the Bn-MS release to investigate microspheres’ in vitro release pattern. The results showed that the addition of appropriate ratios of mixed molecular weights to Bn-MS could eliminate the release hysteresis period. When the ratio of 15 kDa and 75 kDa was 1:9 (F3), the Bn-MS had a low burst release rate, moderate release rate, no release hysteresis period, a long release period of up to 35 days, and a stable release pattern close to the zero level. The results of the release mechanism study indicated that the hybrid PLGA improved the release behavior of the microspheres by adjusting the dissolution degradation rate of Bn-MS, which in turn affected the release mechanism of the microspheres.

Water purification and biological efficacy of green synthesized Co/Zn-Doped α-Fe2O3 nanoparticles

In the present study, Co/Zn doped α-Fe2O3 (Hematite) nanoparticles (NPs) were synthesized using polyvinylpyrrolidone (PVP) and Azadirachta indica (AI) leaves aqueous extract. The analytical techniques including XRD, UV, SEM, EDX, VSM, Raman, and FTIR, we were able to identify and characterize the structural, morphological and magnetic attributes of the synthesized NPs. The findings demonstrated that the synthesized NPs exhibit homogeneous spherical shapes with particle sizes ranging from 8.64 to 15.32 nm. The NPs have rhombohedral crystal lattices, with crystallite sizes of 23.25 nm for chemically synthesized doped α-Fe2O3 NPs and 12.52 nm for those synthesized using green methods. The magnetic study has shown that the saturation magnetization (Ms) value of NPs, which ranges from 36 to 45 emu/g at ambient temperature, exhibits superparamagnetic properties (300 K). The treatment of industrial wastewater and its reuse for agricultural purposes are the subjects of the current study. Different concentrations of doped α-Fe2O3 NPs were used as photocatalysts to degrade dyes in a bioreactor under UV light in a heterogeneous mixture. The degradation rates achieved were 96.42 % for Congo Red (CR) and 98.36 % for Eosin Yellow (EY). DPPH assays were conducted to evaluate the antioxidant activity of the synthesized doped α-Fe2O3 NPs. The percentage inhibition of DPPH radicals ranged from 71.13 % to 90.35 %. Our findings indicate that AI leaf extract holds promise as a valuable resource for the development of bioactive compounds and environmentally friendly approaches to synthesizing green NPs. This is primarily attributed to the increased accessibility of bioactive components with potent antioxidant properties. The combination of these benefits provides opportunities for novel uses in environmental cleanup, biological applications, and energy conversion.

Fabrication of ultrafine Himalayan walnut oil Pickering emulsions by ultrasonic emulsification: Techno-functional properties of emulsions and microcapsules

In present scenario, much of the attention has been put on the production and utilization of Pickering emulsions deciphering enhanced stability and applicability over wide environmental conditions. In this context the present study was carried out to elaborate effect of different wall materials and pH systems on the physicochemical, structural and morphological properties of Himalayan walnut oil Pickering emulsions by ultrasonic emulsification. In this study, concentrated Pickering emulsion of Himalayan walnut oil (HWO) was prepared utilizing soy protein isolate (SPI), maltodextrin (MD) stabilized by pectin at varying concentrations and pH systems (4.0, 7.0). With increase in pectin and SPI concentration and lowering MD, stable emulsions were obtained as deciphered by an Emulsion stability index (ESI) of 100 for 7 days at ambient storage. HWO Pickering emulsions were analysed for particle size measurements (2.13–13.64 µm) and depicted negative zeta potential values (−3.70 to −18.58). Lyophilized HWO microcapsules depicted moderate encapsulation efficiency (44.69–57.63 %) whereas the hygroscopicity values of the microcapsule ranged from (0.21–12.10 %). Thermogravimetric analysis (TGA) of the samples depicted the temperature of maximum degradation rate up to 550 °C whereas XRD spectra depicted amorphous nature of oil microcapsules. FTIR spectra revealed a close association between the SPI-MD-Pectin matrix. SEM analysis revealed stable oil globules entrapped in protein-polysaccharide matrix with no visible cracks and fissures.

Ab initio study of iron-doped zinc oxide for efficient dye degradation

First principle calculations were performed on iron doped zinc oxide (Fe-ZO) to reduce its bandgap to optimize its visible light absorption. The doping of iron in the ZO is done via supercells of Zn1-xFexO. The doped systems are analyzed using generalized gradient approximation plane wave pseudopotential on density functional theory, or local density approximation and LDA + U with PBE. The computational analysis reveals that the bandgap reduced with increasing dopant concentration. Furthermore, a robust absorption is observed toward the visible region of the spectrum. This enhances its ability as a photochemical material to increase degradation rates of industrial grade dyes.

Construction of a novel Z-scheme FeTiO3/MOF-derived In2S3 catalyst for visible-light-driven photo-Fenton degradation of pollutants

The rapid recombination rate of photoexcited carriers for iron titanate (FeTiO3) is still limited the process performance of photo-Fenton. This article reports the successful synthesis of the highly efficient Z-scheme FeTiO3/MOF-derived In2S3 photocatalyst using the hydrothermal method, compensating for the susceptibility of FeTiO3 photo-generated carriers to complexation to a certain extent. A series of characterization have been carried out to explore the structure, morphology and composition of FeTiO3/MOF-derived In2S3 heterostructure. The 0.5 FeTiO3/MOF-derived In2S3 exhibits the excellent photo-Fenton performance for TCH, Cr6+ and OTC, the degradation rate constants (k2) are up to 0.6297 L·mg−1·min−1, 1.332 L·mg−1·min−1, and 0.427 L·mg−1·min−1, respectively. Active species capture experiments and electron paramagnetic resonance (EPR) spectra show that photo-generated holes (h+) and superoxide radicals (·O2-) are present in the photo-Fenton system. The superior photo-Fenton performance is mainly manifested in the following: the MOF-derived In2S3 micro-floral carrier extends the reaction interface of 0.5 FM-I; FeTiO3 effectively enhances the photo-absorption ability of 0.5 FM-I in visible range; the construction of Z-scheme FeTiO3/MOF-derived In2S3, forming the new carriers transport channels and enhancing the generation of ·O2- and ·OH. This experimental exploration provided a reasonable experimental basis for the preparation of efficient photocatalysts.

Synergistic effects of bacteria, enzymes, and cyclic mechanical stresses on the bond strength of composite restorations

Predicting how tooth and dental material bonds perform in the mouth requires a deep understanding of degrading factors. Yet, this understanding is incomplete, leading to significant uncertainties in designing and evaluating new dental adhesives. The durability of dental bonding interfaces in the oral microenvironment is compromised by bacterial acids, salivary enzymes, and masticatory fatigue. These factors degrade the bond between dental resins and tooth surfaces, making the strength of these bonds difficult to predict. Traditionally studied separately, a combined kinetic analysis of these interactions could enhance our understanding and improvement of dental adhesive durability. To address this issue, we developed and validated an original model to evaluate the bond strength of dental restorations using realistic environments that consider the different mechanical, chemical, and biological degradative challenges working simultaneously: bacteria, salivary esterases, and cyclic loading. We herein describe a comprehensive investigation on dissociating the factors that degrade the bond strength of dental restorations. Our results showed that cariogenic bacteria are the number one factor contributing to the degradation of the bonded interface, followed by cyclic loading and salivary esterases. When tested in combinatorial mode, negative and positive synergies towards the degradation of the interface were observed. Masticatory loads (i.e., cycling loading) enhanced the lactic acid bacterial production and the area occupied by the biofilm at the bonding interface, resulting in more damage at the interface and a reduction of 73 % in bond strength compared to no-degraded samples. Salivary enzymes also produced bond degradation caused by changes in the chemical composition of the resin/adhesive. However, the degradation rates are slowed compared to the bacteria and cyclic loading. These results demonstrate that our synergetic model could guide the design of new dental adhesives for biological applications without laborious trial-and-error experimentation.

Toxicological assessment of reactive blue 19 dye aqueous solutions under UV-LED light

Abstract The dye-contaminated industrial effluent causes serious health issues when it gets mixed with underground water without primary treatment. The current project was designed to treat reactive blue-19 dye aqueous solutions in the presence of hydrogen peroxide (H2O2) and titanium dioxide (TiO2) under UV-LED light. The characterization of the photocatalyst was carried out via X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM) for structure, purity, and surface study. The effect of various factors such as pH, TiO2 dose, UV-LED light exposure time, H2O2, and dye concentration, on the degradation rate and cytotoxicity reduction was evaluated and optimized through the Response Surface Methodology (RSM). The maximum degradation of dye solution and chemical oxygen demand (COD) reduction was achieved at 98.81 and 86.22 %, respectively for 50 ppm solution, using UV-LED/H2O2(3 %)/TiO2(6 g/L) hybrid process. The toxicity evaluation through the Allium cepa test demonstrated a 62.40, 65.2, and 56.97 % increase in root length (RL), root count (RC), and mitotic index (MI), respectively, following treatment with the UV-LED/H₂O₂/TiO₂ combined process for 150 min. The hemolytic and brine shrimp tests revealed a reduction in toxicity up to 92.18 and 84.08 %, respectively, after applying the same treatment. Additionally, the Ames test indicated up to 80.94 % reduction in mutagenicity for TA98 and an 84.04 % reduction for TA100 strain when dye samples were treated with UV-LED light in the presence of H₂O₂ and TiO₂ for 150 min. The findings suggested that UV-LED light in conjunction with H2O2 and TiO2 can be a useful tool for the degradation and detoxification of toxic pollutants found in textile wastewater.

From aromatic rings to aliphatic compounds - degradation of duloxetine with the use of visible light driven Z-scheme photocatalyst

The growing consumption of antidepressants, associated with their high chemical stability and low biodegradability, become a serious problem for aquatic environment. Many of their components are resistant to conventional water treatment technologies. The photocatalytic processes with the use of semiconductors becoming attractive methods of drugs degradation because the highly reactive species: electrons, holes, hydroxyl radicals (⦁OH) and superoxide anion radicals (O2⦁−) generated under illumination may be involved directly or indirectly in decomposition of complicated organic molecules.In this work we have shown for the first time that Z-scheme photocatalyst, consisted of bismuth vanadate (BiVO4), graphitic-like carbon nitride (g-C3N4) and Au nanoparticles (Au NPs) as a charge transfer mediator, is very efficient in degradation of duloxetine (DLX). We performed the comprehensive evaluation focused not only on degradation rate, mechanism of photocatalytic process, but also identification of decomposition products and the pathways of DLX degradation. Due to application of the elaborated Z-scheme photocatalyst, the degradation rate constant was more than 2-3 times higher than that obtained for photolysis, but more important, the final compounds were mainly aliphatic products, formed by opening of aromatic rings. The chemical structure of the degradation products were determined with the use of HPLC and LC-MS. The toxicity of photoproducts with respect to water organisms was tested by means of Spirotox and Microtox assays. The Microtox test indicated that toxicity of the products after 6h of the solution irradiation in the presence of Z-scheme photocatalyst is about 4 times lower than that after photolysis.

Applying the driver-pressure-state-impact-response model to ecological restoration: A case study of comprehensive zoning and benefit assessment in Zhejiang Province, China

Ecosystem degradation is a global problem that poses a significant threat to the sustainable development of human societies, particularly in developing countries, such as China. In response, China has implemented a series of ecological restoration (ER) policies over recent years. However, significant regional developmental disparities, pronounced spatial heterogeneity of ecological issues, and substantial historical debt for ER in China present considerable obstacles and financial burdens to the effective implementation of ER strategies. Delineating ER zones and assessing the ER benefits are essential for developing effective ER strategies and implementing ER projects. In this study, we constructed a comprehensive framework for ER utilizing the Driver-Pressure-State-Impact-Response (DPSIR) model, quantified the urbanization levels, ecological state, and restoration costs in Zhejiang Province to delineate ER zones, integrated the patch-generating land use simulation model with the ecosystem service value assessment method to quantify the benefits of ER, and ultimately developed tailored ER strategies. The results showed that: (1) The pattern of urbanization levels was characterized by high levels in the northeast and low levels in the southwest, which constrated with the ecological state. The areas of high restoration costs were located in the northeastern and southeastern regions, and the areas of low restoration costs were situated in the southwestern region. (2) The rate of construction land expansion is significantly curtailed under the ER scenario compared to the natural development scenario in 2035, while forest areas have seen effective protection and an increase from the levels of 2020. (3) The ER policy is projected to generate ecological benefits totaling CNY 8.23 billion by 2035, substantially reducing the rate of ecosystem degradation. (4) Zhejiang Province is divided into five zones at the county scale: ecological autonomous protection zone, ecological core protection zone, ecological priority restoration zone, ecological control zone, and moderate development zone. Strategies have been devised based on the forecasted benefits of ER, offering valuable insights into ecological management. These findings aim to enhance the understanding of ER and support the development and implementation of regional ecological policies.

Microbial Inoculation accelerates rice straw decomposition by reshaping structure and function of Lignocellulose-Degrading microbial consortia in paddy fields

Inoculating lignocellulose-degrading microorganisms can accelerate straw decomposition in paddy field; however, the relationship between indigenous and inoculated microorganisms remains unclear. This study explored the effects of microbial inoculation on straw decomposition, microbial community, lignocellulose-degrading consortia, and associated functional genes. After inoculation, straw degradation rate increased by up to 4.9 %, and the rice yield increased by 790 kg/ha. Microbial inoculation restructured soil microbial community, influencing key taxa and interactions within the microbial network. A lignocellulose-degrading consortia consisting 37 genera was established, with a notable increase in the relative abundance of lignocellulose-degrading bacteria following inoculation. Among them, Pseudarthrobacter, with high lignin-degrading enzyme activity, emerged as a key genus after inoculation. Additionally, the abundance of lignin-degrading enzyme genes also increased significantly after inoculation. These findings offer new insights into how microbial inoculation accelerates the in situ decomposition of rice straw by reshaping the structure and function of lignocellulose-degrading consortia within the soil ecosystem.

Investigation of the effect of human intestinal microbiota bacteria on the bioremediation of commonly used pesticides by liquid chromatography

Pesticides are defined as chemical substances used to protect a variety of plants from parasite infestation. Due to their chemical structure, they have a long half-life and the capacity to form residues, and therefore many fruits can contain pesticide residues. Pesticide exposure may occur via inhalation, ingestion, or direct contact. The European Commission's directive restricts the use of pesticides and sets a residue limit of 0.1 μg/L. The aim of this study is to determine the impact of bacteria in the human gut microbiota on the biodegradation of commonly used pesticides. This study investigated the effects of five bacterial strains, namely Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae (K. pneumoniae), and Enterococcus faecalis (E. faecalis), isolated from neonatal rectal swab samples and, blood samples on the degradation of pesticides using liquid chromatography and mass spectrometry. (LC-MS). All bacteria resulted in significant pesticide degradation (p < 0.05). E. faecalis caused significantly more degradation than K. pneumoniae (p = 0.043). No significant difference was observed between the degradation rates of pesticides and other bacteria (p > 0.05). The results demonstrate that bacteria can be used to clean water and soil contaminated with pesticides. Therefore, we do not have information about possible mutations in DNA. This is the biggest limitation of this study. Therefore, our study data needs to be supported with study data including more strains and examining bacterial DNA with new generation sequencing methods.

VUV Activated Fe(VI) by Promoting the Generation of Intermediate Valent Iron and Hydroxyl Radicals.

In this study, vacuum ultraviolet (VUV) was first proposed to activate ferrate (Fe(VI)) for degrading micropollutants (e.g., carbamazepine (CBZ)). Results indicated that VUV/Fe(VI) could significantly facilitate the CBZ degradation, and the removal efficiencies of VUV/Fe(VI) were 30.9-83.4% higher than those of Fe(VI) at pH = 7.0-9.0. Correspondingly, the degradation rate constants of VUV/Fe(VI) were 2.3-36.0-fold faster than those of Fe(VI). Free radical quenching and probe experiments revealed that the dominant active species of VUV/Fe(VI) were •OH and Fe(V)/Fe(IV), whose contribution ratios were 43.3 to 48.6% and 48.2 to 46.6%, respectively, at pH = 7.0-9.0. VUV combined with Fe(VI) not only effectively mitigated the weak oxidizing ability of Fe(VI) under alkaline conditions (especially pH = 9.0) but also attenuated the deteriorating effect of background constituents on Fe(VI). In different real waters (tap water, river water, WWTPs effluent), VUV/Fe(VI) retained a remarkably enhanced effect on CBZ degradation compared to Fe(VI). Moreover, VUV/Fe(VI) exhibited outstanding performance in the debasement of CBZ and sulfamethoxazole (SMX), as well as six other micropollutants, displaying broad-spectrum capability in degrading micropollutants. Overall, this study developed a novel oxidation process that was efficient and energy-saving for the rapid removal of micropollutants.