Bioprotective Respirator Assembled by Defective Carbon Nitride for Long-Term Light Triggered Health Protection.

Wearing face masks is the best way to stop the spread of respiratory infections. However, if masks are not sterilized, changing them too frequently can actually increase the risk of cross-contamination. Herein, the construction of an antipathogen photocatalytic mask with carbon vacancy-modified carbon nitride nanosheets (g-C3N4-VC Ns) coated on the non-woven fabrics of the out layer of the mask, offering effective and long-term protection against damaging pathogens when exposed to light is reported. The introduced carbon vacancies are found capable of creating energy-disordered sites and inducing energetic electric force to overcome the Coulomb interactions between electron-hole pairs, thus promoting the electron-hole separation to achieve a high generation of reactive oxygen species (ROS). Thanks to its high activity in generating ROS upon exposure to light, the as-prepared photocatalytic mask shows high pathogen sterilization performance. This, in turn, prolongs the mask's protective lifetime, decreases the need for regular replacement, and decreases medical waste production. The work demonstrated here opens new viewpoints in designing pathogens biocidal protective devices for health protection, offering significant promise in specific environment self-protection.

Efficient activation of peroxymonosulfate by CoMg2Mn-LDO for the degradation of orange â ¡: The important synergy of Mg.

Advanced oxidation process (AOP) based on peroxymonosulfate (PMS) has aroused extensive discussion in the degradation of organic pollutants due to the strong oxidative ability of SO4•-. Great attention has been paid to developing transition metal catalysts for PMS activation. Still, few studies focused on the co-catalysis effect of non-redox metals. To study the co-catalysis of Mg and develop a more efficient metal catalyst, the CoMg2Mn-LDO was prepared by a co-precipitation method accompanied by calcination. The material showed an excellent ability for PMS activation. 97.1% of Orange Ⅱ was degraded within 15 min with the reaction rate constant (kobs) of 0.539 min-1 when pH equals 6.7, the dosages of CoMg2Mn-LDO and PMS were 90 mg L-1 and 100 mg L-1, respectively. By contrast, the value of kobs was 0.375 min-1 for the system of Co3Mn-LDO/PMS at the same experimental conditions. The electron paramagnetic resonance (EPR) and quenching experiments results proved the existence of O2•-, SO4•- and HO• in the CoMg2Mn-LDO/PMS system and the dominant role of SO4•- in Orange Ⅱ degradation. The synergistic effects among Co, Mn, and Mg were found to be responsible for the outstanding catalytic ability of CoMg2Mn-LDO. The presence of Mg could not only promote the formation of Mg-HSO5- and CoOH+ complexes but also reduce the leaching of Co and Mn, which accelerated the generation of free radicals and decreased secondary pollution risk. Based on the overall analysis, reasonable activation mechanisms of PMS and possible degradation pathways of Orange Ⅱ in this reaction system were proposed. This work proves that Mg could be applied as an effective co-catalytic element and provides new insight into developing transition metal catalysts for PMS-based AOPs.

Konjac glucomannan/pectin/Ca-Mg hydrogel with self-releasing alkalinity to recover phosphate in aqueous solution.

The combination of polysaccharides can obtain stable, degradable, and environmentally friendly hydrogels, which have broad application prospects in adsorbents assembly. With Ca2+ and Mg2+ as crosslinkers, a new pectin/Konjac glucomannan/Ca-Mg composite hydrogel was prepared for phosphate adsorption by the alkali-thermal co-reaction method. Since Mg(OH)2 can create a suitable pH condition for phosphate adsorption by Ca, Ca and Mg synergistically promoted phosphate adsorption and remained stable in the pH range of 4 to 10. FTIR, SEM-EDS, XRD, XPS, and zero potential analysis corroborated that the hydrogel used Ca and Mg as active sites to trap pollutants by electrostatic adsorption and fix phosphate through complexation to form Mg3(PO4)2·8H2O and CaPO3(OH)2·H2O. Furthermore, it is unnecessary to separate the recovered phosphate from the hydrogel, and it can be used directly as a fertilizer. By being reused in the soil, it promoted seed germination and seedling growth. This adsorbent has the potential for recovery as a phosphorus-containing organic fertilizer after phosphorus adsorption.

Comments on "Facilely synthesized cobalt doped hydroxyapatite as hydroxyl promoted peroxymonosulfate activator for degradation of Rhodamine B".

In recent years, researchers have devoted themselves to developing composites containing cobalt as highly active heterogeneous catalysts of persulfate. Most of them reported that the catalytic degradation processes of organic pollutants were accompanied by the leaching of cobalt ions, but only a few studies considered the contribution of the dissolved cobalt ion to the degradation of organic compounds. A research paper in Journal of Hazardous Materials reported a study on synthesis, application and catalytic mechanisms of cobalt doped hydroxyapatite (Co-HAP) for Rhodamine B (RhB) degradation. We find that non-main catalytic mechanisms were listed and that the effect of Co-HAP was overestimated.

Effects of overwintering cyanobacteria on phosphorus and iron regeneration across the sediment-water interface: A pilot simulation experiment.

Cyanobacterial blooms are a major environmental problem in eutrophic reservoirs in China. Algal cells can migrate to the sediment surface in winter and maintain biological activity, which could further affect the cycling process of sediment phosphorus (P) and iron (Fe). In this study, a pilot simulation experiment was conducted to investigate the effect of overwintering cyanobacteria (Owc) on P and Fe regeneration across the sediment-water interface (SWI). Owc esterase activity ranged from 16.4 to 26.6 nmol (FDA)/(L·h), with a fluctuating increasing trend within the incubation time. Compared with the control (no Owc), Owc treatment increased the redox potential value (Eh) at the SWI but slightly decreased the pH during the first stage of this experiment (0-24 d); however, the Eh at the SWI under Owc treatment decreased to 50.9 % of that of the control on day 90. The Fe(II) could rapidly oxidized to Fe (oxyhydro)oxides and combine with phosphate in high Eh environments, and Owc inhibited P and Fe release at the SWI within 24 days; however, the continuous decrease in Eh resulted in the reduction of Fe(III). Thus, the Fe concentration measured via diffusive gradients in thin films in the Owc-treated interstitial water gradually increased to 1.92 times that of the control, promoting the release of Fe and P across the SWI. For 13 days after Owc addition, the amount of mobile P in the sediment was significantly higher than that in the control, and it gradually decreased from day 24 to 90, with the lowest being approximately 74.1 % of the amount in the control. The reactive Fe concentration in the sediment showed a similar variation trend. These results indicate that mobile P and reactive Fe in the sediment could be the main sources of regeneration across the SWI in the presence of Owc.

Unveiling interactions of norfloxacin with microplastic in surface water by 2D FTIR correlation spectroscopy and X-ray photoelectron spectroscopy analyses.

Microplastics (MPs) has shown adsorption of hydrophilic organic matters (HOMs) in aqueous environments. However, it is still difficult to predict the adsorption behaviors of HOMs by different MPs, especially in authentic water systems. In this study, the adsorption behaviors and mechanisms of norfloxacin (NOR) onto polyamide (PA) MPs were investigated in both simulated and real surface water. The results showed that the adsorption equilibrium of NOR by PA in simulated surface water could be achieved within 15 h, while the adsorption rate of NOR in real surface was slowed down, with the equilibrium time of 25 h. Pseudo-second-order model could well describe the adsorption kinetics data. The experimental maximum adsorption capacity of NOR on PA in real surface water (e. g. 132.54 ug/g) was dramatically reduced by 37.5 % compared with that in simulated surface water (e. g. 212.25 ug/g), and the adsorption isotherm would obey Freundlich model. Besides, the leaching of NOR from the surface of PA could occur obviously at acidic environment. Furthermore, the salinity and natural organic matter exhibited significantly adverse effects on the NOR adsorption. Finally, the results of 2D Fourier transform infrared correlation spectroscopy and X-ray photoelectron spectroscopy indicated that the electrostatic, H-bond and van der Waals interactions were involved in the adsorption. More importantly, the sequential functional groups in the adsorption process followed the orders: 1638 (CO) > 1542 amide II (-NH-CO) > 717 (CH2) > 1445 (CO) > 973 amide IV (CONH). This study could provide an insight into the interactions between PA and NOR in different water environments.

Effects of intercropping ryegrass with hollyhock and inoculation with Bacillus thuringiensis on enhancing phytoremediation of Cd-contaminated soils.

Cd is a heavy metal that contaminates soils. These kinds of heavy metals pose a serious threat to food security, ecosystems, and human health. To improve the phytoremediation efficiency of moderately Cd-contaminated cropland soils and achieve simultaneous production and remediation, intercropping ryegrass (Lolium perenne L.) with hollyhock (Althaea rosea) was investigated using pot experiments, and Bacillus thuringiensis (B. thuringiensis) inoculation was used as a booster to strengthen the absorption and accumulation of Cd in plants. The results showed that intercropping (Int treatment) decreased the Cd concentration in plants compared to hollyhock and ryegrass monocropping. However, the Cd accumulation in ryegrass and hollyhock was promoted by B. thuringiensis addition to intercropping (Int-B treatment), as the biomass of ryegrass and hollyhock was 2.33 and 1.13 times that of the Int treatment, respectively. Compared with the Int treatment, the total Cd concentration in soils of the Int-B treatment decreased by 8.1%, while diethylenetriaminepentaacetic acid solution extracted Cd (DTPA-Cd) increased by 18.2%, indicating that B. thuringiensis increases the available Cd concentration in soils to promote Cd adsorption by hollyhock enrichment plants. High-throughput sequencing results further revealed that the dominant microflora in the soils of the Int and Int-B treatments were consistent with the control, although their abundance and diversity decreased slightly. Overall, intercropping with B. thuringiensis addition effectively increased the hollyhock remediation efficiency in moderately Cd-contaminated soils, and the concentration of Cd in forage crops of ryegrass was lower than the limit value of "Hygienic standards for feeds' (GB 13078-2017) in China.

Nitrogen addition may promote soil organic carbon storage and CO2 emission but reduce dissolved organic carbon in Zoige peatland.

With the increase of nitrogen (N) deposition, N input can affect soil C cycling since microbes may trigger a series of activities to balance the supply and demand of nutrients. However, as one of the largest C sinks on earth, the role of extra N addition in affecting peatland soil C and its potential mechanism remains unclear and debated. Therefore, this study chose the largest peatland in China (i.e., Zoige, mostly N-limited) to systematically explore the potential changes of soil C, microbes, and ecoenzymes caused by extra N input at the lab scale incubation. Three different types of soils were collected and incubated with different levels of NH4NO3 solution for 45 days. After incubation, N input generally increased soil organic C (SOC) but decreased dissolved organic carbon (DOC) in Zoige peatland soils. Moreover, CO2 and CH4 emissions were significantly increased after high N input (equal to 5 mg NH4NO3 g-1 dry soils). Through a series of analyses, it was observed that microbial communities and ecoenzyme activities mainly influenced the changes of different C components. Collectively, this study implied that the increasing N deposition might help C sequestration in N-limited peatland soils; simultaneously, the risk of increased CO2 and CH4 by N input in global warming should not be ignored.

Tetracycline adsorption trajectories on aged polystyrene in a simulated aquatic environment: A mechanistic investigation.

Microplastics (MPs) have attracted widespread attention as an organic class of pollutants as well as pollutant carriers in recipient aquatic ecosystems. In this study, tetracycline (TC) adsorption by polystyrene (PS), with multiple aging-based temporal changes in the adsorption mechanism, was observed. The results revealed that the pseudo-second-order model accurately predicted the TC adsorption kinetics for different types of PS. In addition, the isothermal adsorption processes fit the Freundlich model; however, their interactions were drastically weakened at lower temperatures or increasing salinities. Corresponding to the electrostatic interactions, adsorption TC was largely pH-dependent, with the maximum adsorbed TC content on the PS surface at a pH of 5 in an aqueous environment. More importantly, mechanistic studies have revealed that, compared to virgin PS, TC complexes with aged PS are principally controlled by hydrogen bonding and ionic interactions, followed by π-π, polar-polar, and van der Waals interactions. These findings will aid in understanding the insights of TC and aged PS interactions and the underlying interactive molecular forces, which will be advantageous for comprehending the real case scenario of inter-pollutant interactions and related environmental pollution.

The silicon active sites driven by oxygen vacancies in iron silicate for activating peroxymonosulfate.

Most metal sites and some non-metallic sites such as carbon and nitrogen are usually considered to be traditional active sites during peroxymonosulfate (PMS) activation. However, as an important non-metallic element, the actual role of silicon (Si) in PMS activation still remains unclear. In this work, taking iron silicate (FeSi) as an example, the role of the Si region in PMS activation was clearly revealed. The experiments and density functional theory (DFT) calculation results showed that besides the traditional Fe sites, the Si also played a non-negligible role during PMS activation. In FeSi containing oxygen vacancies (Ovac), Fe-Si was the active site instead of Fe-Fe. The Bard charge results implied that the presence of Ovac tuned the electronic properties of FeSi, making the Si participate in PMS activation. This work deepened understanding of the role of Si in silicates for PMS activation and provided a theoretical basis for the development of excellent Si-based catalysts.

Understanding and characteristics of coagulation removal of composite pollution of microplastic and norfloxacin during water treatment.

Water composite pollution is still a great challenge in the field of water treatment. Especially for microplastic (MP), as an emerging pollutant, its wide distribution in water and persistent eco-environmental influence have received great concerns in recent years. Nevertheless, the removal characteristics and mechanism of conventional coagulation on MP composite pollution is quite insufficient. In this study, the coagulation removal performance and mechanisms of MP (polyethylene, PE) and norfloxacin (NOR) was investigated by polyaluminium chloride (PAC) and anionic polyacrylamide (APAM). Compared with single system, the removal efficiency of PE was significantly improved (>99.0%) under plateau stage in composite system, while the removal efficiency of NOR was slightly decreased to around 42% regardless of the addition of APAM. The scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), zeta potential and One-way analysis of variance (ANOVA) of experimental data were used to explore the coagulation mechanisms. The results demonstrated that the removal of individual PE and NOR was mainly controlled by charge neutralization and sweep flocculation by PAC and APAM, and adsorption by formation of Al-NOR complex, respectively. Importantly, in composite system, the removal of PE was enhanced not only by the stronger charge neutralization but also the adsorption via the formation of PE-NOR-Al complex. Furthermore, the removal efficiency of PE and NOR in neutral and weak alkaline conditions was higher than that in weak acidic or strong alkaline conditions. The presence of metal ions and humic acid had obvious inhibition and promoting effects on the removal efficiency of PE and NOR. This study can provide a new perspective on fundamental understanding in characteristics and mechanisms of MP composite pollutants removed by coagulation.

Distribution of microplastics in the sludge of wastewater treatment plants in chengdu, China.

Large amounts of microplastics can accumulate in wastewater treatment plants (WWTPs), and sludge disposal is suspected to be a major source of microplastics pollution in the environment. It is therefore important to investigate the distribution of microplastics in the sludge of each processing unit of WWTPs. However, little information is available on this topic in China. Accordingly, in this study, the abundance and characteristics of microplastics in the sludge of two WWTPs in Chengdu were investigated. The abundance of microplastics in the sludge samples ranged from 44.4 n·kg-1 to 750.0 n·kg-1. Microplastics were mainly divided into particles (32.16%), debris (28.14%) and fibers (17.08%) according to their shape, and the colors of the microplastics were mainly green (35.19%) and translucent (18.06%). The particle sizes were mainly larger than 1 mm in dimension. Polyethylene, polypropylene and polystyrene were the prevalent types of microplastics analyzed. Our results provide basic information for better understanding the characteristics of microplastics in sludge and for improving sludge treatment.

Insights into lignocellulosic waste fractionation for lignin nanospheres fabrication using acidic/alkaline deep eutectic solvents.

Facile fractionation of lignocellulosic waste into useable forms is essential to achieve a multi-product treatment process especially when the resulting lignin streams are expected for high-value materials valorization. Despite acidic/alkaline deep eutectic solvents (DESs) are promising solvents for lignocellulosic waste fractionation, there is little information about their differences in the fractionation and lignin extraction profiles. In this work, four DESs that were cataloged to acidic types (formic acid-choline chloride, lactic acid-choline chloride) and alkaline types (monoethanolamine-choline chloride, glycerol-K2CO3) were investigated to compare their abilities of bamboo waste fractionation. Physicochemical properties of these resulting cellulose, lignin and derived lignin nanospheres (LNPs) were also assessed. Results showed that DESs could selectively extract lignin via cleaving lignin-carbohydrate linkages and lignin ether bonds. Acidic DESs pretreatments were more effective in biomass delignification (~95.0 %), while alkaline DESs showed better polysaccharide retention. Glycerol-K2CO3 LNPs exhibited much smaller sphere size (50-100 nm) while acidic DESs LNPs showed higher thermal stability due to higher extent of lignin condensation. In addition, MEA-ChCl could introduce amine groups onto lignin hydroxyl. This work provided insightful information for tailoring technique routes to selective lignocellulosic waste fractionation, while facilitating the downstream applications of the obtained cellulose/lignin.

Self-generated peroxyacetic acid in phosphoric acid plus hydrogen peroxide pretreatment mediated lignocellulose deconstruction and delignification.

BACKGROUND: Peroxyacetic acid involved chemical pretreatment is effective in lignocellulose deconstruction and oxidation. However, these peroxyacetic acid are usually artificially added. Our previous work has shown that the newly developed PHP pretreatment (phosphoric acid plus hydrogen peroxide) is promising in lignocellulose biomass fractionation through an aggressive oxidation process, while the information about the synergistic effect between H3PO4 and H2O2 is quite lack, especially whether some strong oxidant intermediates is existed. In this work, we reported the PHP pretreatment system could self-generate peroxyacetic acid oxidant, which mediated the overall lignocellulose deconstruction, and hemicellulose/lignin degradation. RESULTS: The PHP pretreatment profile on wheat straw and corn stalk were investigated. The pathways/mechanisms of peroxyacetic acid mediated-PHP pretreatment were elucidated through tracing the structural changes of each component. Results showed that hemicellulose was almost completely solubilized and removed, corresponding to about 87.0% cellulose recovery with high digestibility. Rather high degrees of delignification of 83.5% and 90.0% were achieved for wheat straw and corn stalk, respectively, with the aid of peroxyacetic acid oxidation. A clearly positive correlation was found between the concentration of peroxyacetic acid and the extent of lignocellulose deconstruction. Peroxyacetic acid was mainly self-generated through H2O2 oxidation of acetic acid that was produced from hemicellulose deacetylation and lignin degradation. The self-generated peroxyacetic acid then further contributed to lignocellulose deconstruction and delignification. CONCLUSIONS: The synergistic effect of H3PO4 and H2O2 in the PHP solvent system could efficiently deconstruct wheat straw and corn stalk lignocellulose through an oxidation-mediated process. The main function of H3PO4 was to deconstruct biomass recalcitrance and degrade hemicellulose through acid hydrolysis, while the function of H2O2 was to facilitate the formation of peroxyacetic acid. Peroxyacetic acid with stronger oxidation ability was generated through the reaction between H2O2 and acetic acid, which was released from xylan and lignin oxidation/degradation. This work elucidated the generation and function of peroxyacetic acid in the PHP pretreatment system, and also provide useful information to tailor peroxide-involved pretreatment routes, especially at acidic conditions.

The fate of antibiotic resistance genes and their influential factors during excess sludge composting in a full-scale plant.

The alteration of antibiotic resistance genes (ARGs) during sludge composting has been less studied in a full-scale plant, causing the miss of practical implications for understanding/managing ARGs. Therefore, this study tracked the changes of ARGs and microbial communities in a full-scale plant engaged in excess sludge composting and then explored the key factors regulating ARGs through a series of analyses. After composting, the absolute and relative abundance of ARGs decreased by 91.90% and 66.57%, respectively. Additionally, pathway analysis showed that MGEs, composting physicochemical properties were the most vital factors directly influencing ARGs. Finally, network analysis indicated that Proteobacteria, Bacteroidetes, Firmicutes, and Actinobacteria were the main hosts of ARGs. Based on these findings, it can be known that full-scale composting could reduce ARGs risk to an extent.

Mechanistic insight into different adsorption of norfloxacin on microplastics in simulated natural water and real surface water.

Microplastics (MPs) as carriers of various contaminants have attracted more attentions in water environments. However, the interactions between typical MPs and norfloxacin (NOR) in natural water environments were still not systematically studied. In this study, the adsorption of NOR onto four typical types of MPs (polyethylene (PE), polypropylene (PP), polystyrene (PS), and polyvinyl chloride (PVC)) was investigated in simulated natural water and real surface water, and the adsorption mechanisms were deeply explored to provide fundamental understandings of the MPs-NOR complicated pollution. The results showed that the kinetics of NOR onto all MPs obeyed pseudo-second-order model, and was greatly slowed down at lower temperature or higher salinity. The intrinsic structure and surface area of MPs played important roles in the adsorption behaviors of NOR on these four types of MPs. The adsorption isotherm of NOR onto all MPs could be well described by linear model, with the Kd values following the order of PVC > PS > PE > PP (i.e. 6.229-11.901 L/µg) in simulated natural water. However, in surface water the adsorption isotherms of NOR on all MPs could be well fitted by Freundlich model. For all MPs, the adsorption of NOR was quite pH-dependent due to the electrostatic interactions. Furthermore, the salinity and the presence of dissolved organic matter (DOM) had significantly hindered the NOR adsorption. More importantly, compared with adsorption behaviors in simulated natural water, the competition of coexisting substances such as cations and NOM for adsorption sites and higher water pH dramatically reduced the adsorption of NOR onto all types of MPs in Jiang'an River, with the reduction rate of 19.7-41.2%. Finally, the mechanism studies indicated that the electrostatic attractions played a key role in the adsorption of NOR onto MPs, and π-π, H-bonding, polar-polar, and Van Der Waals interactions were also involved in adsorption processes.

Highly efficient removal of phosphorus from agricultural runoff by a new akadama clay barrier-vegetated drainage ditch system (VDD) and its mechanism.

A vegetated drainage ditch (VDD) system is an effective management practice for removing excess phosphorus (P) from agricultural runoff. However, the maximization of P removing efficiency by VDD remains a challenge. In this study, new VDDs with akadama clay barriers (particle size of clay: 1-6 mm; height of barrier: 5-15 cm and length of barrier: 10-90 cm) were designed in lab scale, and the mechanism of phosphate removal by akadama clay was investigated. It was found that a new VDD with akadama clay barriers (particle size:1 mm; height:10 cm and length: 90 cm) exhibited the highest removal efficiency of total P (TP) (97.1%), particulate P(PP) (96.9%), and dissolved P (DP) (97.4%), respectively. The retained P was mainly adsorbed in akadama clay barrier sections, and a low concentration of P was observed in soil sections in the new VDD. The maximum adsorption capacity of phosphate to akadama clay was 5.06 mg/g at 298 K, and XPS analysis indicated that phosphate was adsorbed by the inner-sphere complexation formation with the metal elements (Al, Fe). This study indicates that the new VDD with akadama clay barriers is a promising technique to efficiently remove P from agricultural runoff and significantly minimize the risk of P release into streams through runoff.

3-D hierarchical porous carbon from oxidized lignin by one-step activation for high-performance supercapacitor.

To convert lignin into high-valued carbon materials and understand the lignin structure function, oxidized lignin, a by-product from lignocellulose PHP-pretreatment (phosphoric acid plus hydrogen peroxide), was carbonized by one-step KOH-activation; the physico-chemical characteristics and electrochemical performances of the harvested carbons were also investigated. Results indicated the resultant carbons displayed 3-dimensional hierarchical porous morphology with maximum specific surface area of 3094 m2 g-1 and pore volume of 1.72 cm3 g-1 using 3:1 KOH/lignin ratio for carbonization. Three-electrode determination achieved a specific capacitance of 352.9 F g-1 at a current of 0.5 A g-1, suggesting a superior rate performance of this carbon. Two-electrode determination obtained an excellent energy density of 9.5 W h kg-1 at power density of 25.0 W kg-1. Moreover, 5000 cycles of charge/discharge reached 88.46% retention at 5 A g-1, implying an outstanding cycle stability. Basically, low molecular weight and abundant oxygen-containing functional groups of employed lignin mainly related to the excellent porous morphology and the outstanding electrochemical performances, suggesting the oxidized lignin was an ideal precursor to facilely prepare activated carbon for high-performance supercapacitor. Overall, this work provides a new path to valorize lignin by-product derived from oxidative pretreatment techniques, which can further promote the integrality of lignocellulose biorefinery.

Why can hydrothermally pretreating lignocellulose in low severities improve anaerobic digestion performances?

A lignocellulosic residue, rice straw, was hydrothermally pretreated for the whole slurry anaerobic digestion. In contrast to the unpretreated rice straw, 110-120 °C pretreatment promoted biogas yield by 35%-38%, while only 14% promotion happened on the pretreatment at 180 °C. To understand why this improvement happened at lower severities, the pretreated rice straw at 90 °C, 120 °C, and 180 °C were selected for the further investigation, in which the liquor and solid fraction were separated for digestion, and compared with the whole slurry digestion. Results indicated more methane was released from the derived liquor of 180 °C than that of 90 °C and 120 °C, however, solid fraction did not exhibit significantly different methane yields (187.77-193.91 mL/g TS). These results suggested that the released soluble fraction from pretreatment could facilitate the methanogenesis. Furthermore, the released inherent soluble fraction in rice straw was mainly responsible for higher biogas yield at lower temperatures. Pretreatment at higher temperatures disintegrated the rice straw recalcitrance more, and intensified the release of soluble fraction accordingly. Consequently, the methanogenesis of whole slurry could be promoted at the initial digestion; the hydrolysis/acidification of the solid fraction in whole slurry was weakened greatly, which resulted in a lower biogas yield. This can also be proved by the evolution of dominant bacteria and archaea in the anaerobic digestion of whole slurry, separated solid and liquor fraction.

Synthesis of a novel anti-fog and high-transparent coating with high wear resistance inspired by dry rice fields.

During the outbreak of COVID-19, the fogging of goggles was a fatal problem for doctors. At present, there are many ways to prevent fogging by adjusting surface wettability. However, the mechanical properties of most super-hydrophilic antifogging coatings are poor, easy to lose their antifogging properties when encountering fingers or cloth friction. To address this issue, the Konjac Glucomannan was cross-linked with water-soluble silicone fluid to form a binder, then being combined with the modified Ecokimera to prepare an eco-friendly super-hydrophilic coating that possessed excellent super-hydrophilicity, and the water contact angle (WCA) was 2.51 ± 1°. In addition, the WCA is still about 5° after 180 times of antifogging tests. The friction resistance of the coating was as high as 24 m. Moreover, the light transmittance was only reduced by 3%. Besides, they also had the excellent self-cleaning property. After being stored in the laboratory environment for 90 days, it can still maintain the hydrophilic property (WCA is about 5°). In general, the method proposed in this study is low-cost and eco-friendly, and can be widely used in the preparation of antifogging coatings.