Humic-like Acids Research Articles

Sodium lignosulfonate-assisted alkaline hydrothermal pretreatment improves the production of humic-like substances from lignocellulosic biomass waste residues

In order to provide key precursors for humic-like substances formation via alkaline hydrothermal pretreatment (AHP), this study introduced an innovative approach by incorporating sodium lignosulfonate (SL) into the AHP to boost the production of humic-like acid (HLA) and fulvic-like acid (FLA) from biomass wastes. The SL-AHP conditions were optimized, and structural analysis of HLA was performed. The highest HLA yield reached 21.90 %, and FLA content reached 13.38 g/L after SL-AHP at 200 °C for 2 h with 15 g/L SL. The inclusion of SL led to a 19.67 % increase in HLA yield and a 5.25-fold enhancement in FLA content compared to that without SL. The probable reason underlying SL's facilitation of HLA and FLA formation involved the effective dissolution of lignin and hemicelluloses to produce more precursors, as well as the incorporation of SL structure into the HLA molecule. SL acted as both a surfactant and a precursor for the production of HLA and FLA. In addition, an increase in acidic groups improved the quality of HLA.

Removal of refractory humic acid-like components from UF filtrate of landfill leachate through pH adjustment and coupled electrochemical process

Mature landfill leachate contains large quantities of a wide range of hazardous and refractory pollutants, especially humic acid-like (HA) and fulvic acid-like (FA) substances. These have poor biodegradability and a considerable ultraviolet-light quenching capacity, severely inhibiting the performance of wastewater treatment and post ultraviolet-light disinfection, but this aspect has attracted little previous research. The Fenton reaction has proved to be a feasible method for removing ultraviolet-quenching substances (UVQSs) but in conventional systems it is unable to completely mineralize organic contaminants. In this study, a novel electro-oxidation process was developed consisting of a flow-through reactor with a Cu2O cathode to catalyze Fenton-type reactions, and oxidation at a RuO2 anode. The combination of pH adjustment and electro-oxidation was evaluated for the treatment of real ultrafiltration (UF) filtrate of mature landfill leachate. A series of analytical techniques were used to determine the performance for the removal of HA and FA. Under optimal conditions, the elimination of fluorescence characteristics of HA and FA reached 100 % and 99.3 %, respectively, according to PARAFAC results based on EEM spectra. TOC was removed by 25.5 %∼30.4 % during the pH adjustment step and 51 % by electrochemical oxidation. Changes in the molecular weight distribution and fluorescence content showed that pH adjustment played an important and significant role in removing UVQSs, and the remaining TOC after electrochemical oxidation was attributed to bioavailable amino acid-like substances. Overall, the results have demonstrated the successful development of an effective method of treating the UF filtrate from mature landfill leachate, with particular respect to the removal of the problematic HA and FA content.

Highly efficient and secure recycling of neomycin fermentation residue by optimum temperature: Nutrients release, neomycin degradation and safety evaluation

The neomycin fermentation residues (NFR) are a solid waste during neomycin production, possessing high recycling value due to their rich organic content. However, the environmentally friendly use of NFR was hindered by its rigid matrix structure and residual neomycin. In this study, the effect of temperature on the structure and bioresource properties of NFR were investigated. Meanwhile, the effect of temperature on the degradation of residual neomycin, the toxicity of neomycin degradation products, and the safety of NFR were assessed. The results indicated that the content of soluble organic matter was increased by appropriate temperature treatment through the disruption of the rigid matrix structure of the NFR. However, excessively high temperatures led to the mineralization of organic matter. Simultaneously, appropriate temperature facilitated the transformation of organic substances to humic-like acids. The neomycin in NFR was effectively degraded with the increasing temperature, and the degradation efficiency exceeded 99 % under 220 °C for 120 min. In addition, the applicability of using appropriate temperatures to degrade antibiotics in similar other AFR has been demonstrated. Neomycin degradation occurred primarily through the cleavage of the glycosidic bond and ring ether, the detachment of the amino group, and the addition of hydroxyl groups. Meanwhile, the developmental toxicity and acute toxicity of neomycin were effectively mitigated by the appropriate temperature, and a significant reduction in ecotoxicity was observed. As a result, optimum temperature treatment proved to be an efficient method for the secure recycling of NFR.

Enhancing humic acids production from cornstalk under fast hydrothermal conditions: Insights into new pathways of skeleton self-polymerization and branch growth

Hydrochar, a sustainable fertilizer rich in humic substances, is made from lignocellulose through hydrothermal conversion. However, hydrothermal humification (HTH) is challenged by low yields and limited selectivity in the resulting hydrochar. This study proved humic-like acids production can be enhanced under fast non-catalytic conditions (260 ∼ 280 °C, 0 ∼ 1 h). A higher yield (by 14.1 %) and selectivity (by 40.2 %) in hydrochar of humic-like acids than conventional HTH (＜250 °C) were achieved. Meanwhile, decreased lignin derivatives, carbonyl and quinone groups, as well as increased sp2-C structures in the humic-like acids were observed. The synthesized humic-like acids exhibited a lower degree of aromatization and a higher molecular weight than commercial variants. Two pathways of humic-like acids formation of self-polymerization and the development of branched sidechains were hypothesized based on mass mitigation, carbon flow and aqueous phase compositions. This research contributes a novel approach to producing humic-like acids rich hydrochar for environmentally friendly fertilizer production.

Changes in the Glucose Concentration Affect the Formation of Humic-like Substances in Polyphenol-Maillard Reactions Involving Gibbsite.

The polyphenol-Maillard reaction is considered one of the important pathways in the formation of humic-like substances (HLSs). Glucose serves as a microbial energy source that drives the humification process. However, the effects of changes in glucose, particularly its concentration, on abiotic pathways remain unclear. Given that the polyphenol-Maillard reaction requires high precursor concentrations and elevated temperatures (which are not present in soil), gibbsite was used as a catalyst to overcome energetic barriers. Catechol and glycine were introduced in fixed concentrations into a phosphate-buffered solution containing gibbsite using the liquid shake-flask incubation method, while the concentration of glucose was controlled in a sterile incubation system. The supernatant fluid and HLS components were dynamically extracted over a period of 360 h for analysis, thus revealing the influence of different glucose concentrations on abiotic humification pathways. The results showed the following: (1) The addition of glucose led to a higher degree of aromatic condensation in the supernatant fluid. In contrast, the supernatant fluid without glucose (Glu0) and the control group without any Maillard precursor (CK control group) exhibited lower degrees of aromatic condensation. Although the total organic C (TOC) content in the supernatant fluid decreased in all treatments during the incubation period, the addition of Maillard precursors effectively mitigated the decreasing trend of TOC content. (2) While the C content of humic-like acid (CHLA) and the CHLA/CFLA ratio (the ratio of humic-like acid to fulvic-like acid) showed varying increases after incubation, the addition of Maillard precursors resulted in a more noticeable increase in CHLA content and the CHLA/CFLA ratio compared to the CK control group. This indicated that more FLA was converted into HLA, which exhibited a higher degree of condensation and humification, thus improving the quality of HLS. The addition of glycine and catechol without glucose or with a glucose concentration of 0.06 mol/L was particularly beneficial in enhancing the degree of HLA humification. Furthermore, the presence of glycine and catechol, as well as higher concentrations of glucose, promoted the production of N-containing compounds in HLA. (3) The presence of Maillard precursors enhanced the stretching vibration of the hydroxyl group (-OH) of HLA. After the polyphenol-Maillard reaction of glycine and catechol with glucose concentrations of 0, 0.03, 0.06, 0.12, or 0.24 mol/L, the aromatic C structure in HLA products increased, while the carboxyl group decreased. The presence of Maillard precursors facilitated the accumulation of polysaccharides in HLA with higher glucose concentrations, ultimately promoting the formation of Al-O bonds. However, the quantities of phenolic groups and phenols in HLA decreased to varying extents.

Transformation of dissolved organic matter during groundwater arsenite removal using air cathode iron electrocoagulation

Dissolve organic matters (DOM) usually showed negative effect on the removal of inorganic arsenic (As) in groundwater by electrochemical approaches, yet which parts of sub-component within DOM played the role was lack of evidence. Herein, we investigated the effects of land-source humic-like acid (HA) on groundwater As(III) removal using air cathode iron electrocoagulation, based on the parallel factor analysis of three-dimensional excitation–emission matrix and statistical methods. Our results showed that the land-source HA contained five kinds of components and all components presented significantly negative correlations with the removal of both As(III) and As(V). However, the high aromatic fulvic-like acid and low aromatic humic-like acid components of land-source HA presented the opposite correlations with the concentration of As(III) during the reaction. The high aromaticity fulvic-like components of land-source HA (Sigma-Aldrich HA, SAHA) produced during the reaction facilitated the oxidation of As(III) due to its high electron transfer capacities and good solubility in wide pH range, but the low aromaticity humic-like ones worked against the oxidation of As(III). Our findings offered the novel insights for the flexible activities of DOM in electron Fenton system.

Dissolved Organic Matter Behaviour by Conventional Treatments of a Drinking Water Plant: Controlling Its Changes with EEM-PARAFAC

In the last 20 years, several articles related to the use of fluorescence excitation–emission matrices—parallel factor analysis (EEM-PARAFAC) to monitor dissolved organic matter (DOM) in drinking- and wastewater treatment plants were published. Noteworthy, its use in respective quality control laboratories remains scarce. To extend its popularisation, in this work, EEM-PARAFAC was employed to analyse the DOM composition changes along the different stages of the drinking water treatment plant administrated by Società Metropolitana Acque Torino. The best PARAFAC model was the one of three components, indicating that the Po River is constituted, mainly, by humic acid-like (HA-L) and tryptophan-like (Try-L) substances, the tyrosine-like ones being negligible (Tyr-L). Results indicated that physical treatments (sedimentation) did not produce a reduction in the PARAFAC scores; however, a 50% decay in 254 nm absorbance was observed. Fluorescent DOM was only removed with chemical treatments, obtaining ca. 70% HA-L scores decay with ozonation and 40% with chlorination. Furthermore, although ozonation degraded HA-L substances, the Try-L scores increased by 25%, indicating the transformation of HA-L into smaller molecules. On the contrary, total organic carbon measurements only exhibited a significant change when comparing the treatment plant’s inlet and outlet (approximately a 45% decrease), but not within intermediate processes.

Bacteria Affect the Distribution of Soil-Dissolved Organic Matter on the Slope: A Long-Term Experiment in Black Soil Erosion

Soil erosion results in dissolved organic matter (DOM) loss and is one of the main paths of soil carbon loss. Bacteria affect the generation and transformation of DOM. However, the effect of bacteria on the composition and slope distribution of DOM has rarely been investigated under field conditions. Based on a long-term experiment of three gradients (3°, 5°, 8°) in a black soil erosion area of Northeast China, the content, composition, and source of DOM were studied. The results showed that the DOM of the 3° and 5° slope was enriched midslope, and the DOM of the 8° slope was enriched downslope. Parallel factor (PARAFAC) analysis indicated that the main substances in DOM were fulvic-like acid, humic-like acid, tryptophan-like protein, and soluble microbial metabolites. The upslope and downslope soils of 3° and 5° slopes showed high DOM bioavailability, while the downslope soil of the 8° slope showed high DOM bioavailability. The content of new DOM in downslope soil increased with the gradient. Bacteria played an important role in the synthesis and transformation of DOM and affected its composition and slope distribution. Verrucomicrobiota, Firmicutes, Planctomycetota, and Gemmatimonadota were the main factors affecting soil DOM. The results could be helpful in understanding the loss mechanism of DOM in eroded black soil and provide support for soil carbon sequestration.

The potential of ferrihydrite-synthetic humic-like acid composite as a soil amendment for metal-contaminated agricultural soil: Immobilization mechanisms by combining abiotic and biotic perspectives

In-situ passivation technique has attracted increasing attention for metal-contaminated agricultural soil remediation. However, metal immobilization mechanisms are mostly illustrated based on metal speciation changes and alterations in soil physicochemical properties from a macroscopic and abiotic perspective. In this study, a ferrihydrite-synthetic humic-like acid composite (FH-SHLA) was fabricated and applied as a passivator for a 90-day soil incubation. The heavy metals immobilization mechanisms of FH-SHLA were investigated by combining both abiotic and biotic perspectives. Effects of FH-SHLA application on soil micro-ecology were also evaluated. The results showed that the 5%FH-SHLA treatment significantly decreased the DTPA-extractable Pb, Cd and Zn by 80.75%, 46.82% and 63.63% after 90 days of incubation (P < 0.05), respectively. Besides, 5% FH-SHLA addition significantly increased soil pH, soil organic matter content and cation exchange capacity (P < 0.05). The SEM, FTIR, and XPS characterizations revealed that the abiotic metal immobilization mechanisms by FH-SHLA included surface complexation, precipitation, electrostatic attraction, and cation-π interactions. For biotic perspective, in-situ microorganisms synergistically participated in the immobilization process via sulfide precipitation and Fe mineral production. FH-SHLA significantly altered the diversity and composition of the soil microbial community, and enhanced the intensity and complexity of the microbial co-occurrence network. Both metal bioavailability and soil physiochemical parameters played a vital role in shaping microbial communities, while the former contributed more. Overall, this study provides new insight into the heavy metal passivation mechanism and demonstrates that FH-SHLA is a promising and environmentally friendly amendment for metal-contaminated soil remediation.

Waste milk humification product can be used as a slow release nano-fertilizer

The demand for milk has increased globally, accompanied by an increase in waste milk. Here, we provide an artificial humification technology to recycle waste milk into an agricultural nano-fertilizer. We use KOH-activated persulfate to convert waste milk into fulvic-like acid and humic-like acid. We mix the product with attapulgite to obtain a slow-release nano fulvic-like acid fertilizer. We apply this nano-fertilizer to chickweeds growing in pots, resulting in improved yield and root elongation. These results indicate that waste milk could be recycled for agricultural purposes, however, this nano-fertilizer needs to be tested further in field experiments.

Overlooked abiotic humification for kanamycin removal in kanamycin fermentation waste by tea polyphenols: New, environmentally friendly and specific

Kanamycin, a typical aminoglycoside antibiotic, is mainly used for the treatment of diseases in humans or animals, while the related antibiotic pollution has been regarded as a serious issue. In this study, a green novel approach to remove kanamycin was established, specifically, kanamycin was specifically removed through abiotic humification process with tea polyphenols (TPs) as the polyphenol donor. The results demonstrated that the kanamycin could be effectively removed by TPs under alkaline conditions, with a 99.9 % highest removal efficiency. Among the three factors (pH, temperature and MnO2 dosage) selected in this study, pH was the most critical factor, with an increase in reaction pH (>6.0) leading to a higher kanamycin removal efficiency, and the temperature and MnO2 dosage ranked as the second and third important factor. Furthermore, kanamycin was mainly removed by being transformed into humic-like acid (HLA) product, and the product antimicrobial activity could be significantly reduced (≥27). Finally, satisfying removal efficiency of kanamycin were observed during the application of TPs in kanamycin fermentation wastewater and kanamycin mycelial residue (KMR), with the highest kanamycin removal efficiency was 99.9 %, and 99.6 %, respectively. This study could also offer insights for the removal of other pollutants containing primary amine or polyphenols.

Straw mulching alters the composition and loss of dissolved organic matter in farmland surface runoff by inhibiting the fragmentation of soil small macroaggregates

Straw mulching is a widespread practice for reducing the soil carbon loss caused by erosion. However, the effects of straw mulching on dissolved organic matter (DOM) runoff loss from black soil are not well studied. How straw mulching affects the composition and loss of runoff DOM by changing soil aggregates remains largely unclear. Here, a straw mulching treatment was compared to a no mulching treatment (as a control) on sloping farmland with black soil erosion in Northeast China. We divided the soil into large macroaggregates (>2 mm), small macroaggregates (0.25–2 mm), and microaggregates (<0.25 mm). After five rain events, the effects of straw mulching on the concentration (characterized by dissolved organic carbon (DOC)) and composition (analyzed by fluorescence spectroscopy) of runoff and soil aggregate DOM were studied. The results showed that straw mulching reduced the runoff amount by 54.7%. Therefore, although straw mulching increased the average DOC concentration in runoff, it reduced the total runoff DOM loss by 48.3%. The composition of runoff DOM is similar to that of soil, as both contain humic-like acid and protein-like components. With straw mulching treatment, the protein-like components in small macroaggregates accumulated and the protein-like components in runoff declined with rain events. Fluorescence spectroscopy technology may help in understanding the hydrological paths of rain events by capturing the dynamic changes of runoff and soil DOM characteristics. A variation partitioning analysis (VPA) indicated that the DOM concentration and composition of microaggregates explained 68.2% of the change in runoff DOM from no mulching plots, while the change in runoff DOM from straw mulching plots was dominated by small macroaggregates at a rate of 55.1%. Taken together, our results demonstrated that straw mulching reduces the fragmentation of small macroaggregates and the loss of microaggregates, thus effecting DOM compositions in soil and reducing the DOM loss in runoff. These results provide a theoretical basis for reducing carbon loss in sloping farmland.

Accelerated spent coffee grounds humification by heat/base co-activated persulfate and products’ fertilization evaluation

Coffee, as the second most common beverage in the world, produced 60% of spent coffee grounds (SCG) with per ton of coffee beans processed. SCG is a typical lignocellulosic-rich organic waste and mainly disposed via composting or incineration. In this study, a rapid humification approach was proposed for the recycling of SCG using heat/base co-activated persulfate (heat/KOH/PS) advanced oxidation process. The yields of humic-like acid (HLA) and fulvic-like acid (FLA) reached 45 (3.96%) and 192 mg/g (19.2%) under the optimal humification conditions of 1% PS and 4% KOH at 100 ℃ in 1 h. The typical active groups of -OH and -COOH in FA standard were observed with higher amounts in the product compared to SCG, which may be related to occurrence of hydroxylation, carboxylation and Maillard reactions during humification. Radicals of •OH and SO4•- were identified in heat/KOH/PS system and made significant contribution to SCG humification. A slow-release nano FLA fertilizer (SNFF) was prepared by mixing treated SCG with attapulgite and showed good slow-release behaviors of HLA and FLA. In pot experiments with acid soil, SNFF increased the average root length of chickweeds by 233% compared with blank. Meanwhile, SNFF also contributed to increased abundance and richness of soil microbial community as well as a pH rise from 5 to 6.7, which was conducive to acid soil amendment. The earthworm test indicated positive ecological safety of SNFF. Overall, this study highlights an efficient humification method for the recycling of organic biowaste such as SCG in green agriculture.

Integrated production of humic-like acid, fulvic-like acid, and fermentable sugars from industrial xylooligosaccharides manufacturing waste residues via hydrothermal pretreatment

Commercial humic substances (HS) are usually extracted from non-renewable resources such as lignite and coal. In this study, artificial HS (mainly humic-like acid (HLA) and fulvic-like acid (FLA)) was produced from renewable biomass-alkaline xylooligosaccharides manufacturing waste residue (XOR) of corncob via hydrothermal pretreatment (HP), as well as fermentable sugars were coproduced. The HLA yield was highest at 1.5% and the content of FLA was 9.6 g/L after HP at 210 °C for 8 h. The glucose yield of HP-pretreated XOR reached 98.8% at CTec 2 dosages of 20 FPU/g glucan. Structural characterization analysis proved that the structures and compositions of HLA were similar to those of commercial humic acid. The results of mass balance indicated that 100 g of XOR yielded 1.5 g of HLA, 9.6 g of FLA, and 60.4 g of monosaccharides (46.9 g of glucose and 13.5 g of xylose). Therefore, this work provides a promising strategy for valorization of lignocellulosic biomass in producing HLA, FLA, and fermentable sugars.

Characteristics in dissolved organic matter and disinfection by-product formation during advanced treatment processes of municipal secondary effluent with Orbitrap mass spectrometry

Dissolved organic matter (DOM) is reported to be a precursor to disinfection by-products (DBPs), which have adverse effects on human health. Therefore, it is crucial to effectively remove DOM before water disinfection. Characteristics of DOM and DBPs formation during advanced treatment processes including coagulation, adsorption, ultraviolet (UV) irradiation, and ozone (O3) oxidation in municipal secondary effluent were investigated in this research. DOM was characterized by Fourier transform infrared spectroscopy (FTIR), excitation-emission matrix fluorescence spectroscopy (EEM), and Orbitrap mass spectrometry (Orbitrap MS). Moreover, DBPs formation potential under different advanced treatment processes was also discussed. FTIR results indicated that various functional groups existing in DOM may react with the disinfectant to form toxic DBPs. EEM analysis indicated that DOM in all water samples was dominated by soluble microbial product-like (SMPs) and humic acid-like (HA) substances. The municipal secondary effluent was abundant with DOM and rich in carbon, hydrogen, oxygen, and nitrogen atoms, contained a certain dosage of phosphorus and sulfur atoms, and the highest proportion is lignin. Most of the precursors (CHO features) had positive double bond equivalent subtracted oxygen per carbon [(DBE-O)/C] and negative carbon oxidation state (Cos) in all four different advanced treatment processes. DBPs formation potential (DBPFP) of coagulation, adsorption, UV irradiation, and O3 oxidation advanced treatment processes were 487 μg L−1, 586 μg L−1, 597 μg L−1, and 308 μg L−1, respectively. And the DBPs precursors removal efficiency of coagulation, adsorption, UV irradiation, and O3 oxidation advanced treatment processes were 50.8%, 40.8%, 39.8%, and 69.0%, respectively. This study provides in-depth insights into the changes of DOM in municipal secondary effluent at the molecular level and the removal efficiency of DBPs precursors during coagulation, adsorption, UV irradiation, and O3 oxidation advanced treatment processes.

Two-Step Hydrothermal Pretreatments for Co-Producing Xylooligosaccharides and Humic-like Acid from Vinegar Residue

This study proposes an efficient strategy for co-producing high-value-added xylooligosaccharides (XOS) and humic-like acid (HLA) from vinegar residue based on two-step hydrothermal pretreatments. During the first-step hydrothermal pretreatment (170 °C, 50 min), 29.1% of XOS (X2-X6) was obtained. The XOS yield was further improved to 36.2% with endoxylanase hydrolysis, thereby increasing the value of (X2-X4)/XOS from 0.8 to 1.0. Subsequently, the second-step hydrothermal pretreatment was investigated to produce HLA from the solid residue of the first-step hydrothermal pretreatment. The highest HLA yield was 15.3% in the presence of 0.6 mol/L of KOH at 210 °C for 13 h. In addition, 31.7% of hydrochar by-product was obtained. The mass balance results showed that 1000 g of vinegar residue produced 67.9 g of XOS, 91.6 g of HLA, and 189.5 g of hydrochar. Therefore, this study provides a promising pathway for comprehensive use of lignocellulosic biomass in producing XOS and HLA.

Influences of Anthropogenic Pollution on the Dynamics of Sedimentary Fulvic Acid Fractions as Revealed via Spectroscopic Techniques Combined with Two-Dimensional Correlation Spectroscopy

To identify the influences of anthropogenic activities on the composition, spatial distribution, sources, and transformation mechanism of sedimentary fulvic acid (FA) fractions from different reaches of an urban river were tracked via excitation-emission matrix (EEM) fluorescence spectroscopy with parallel factor (PARAFAC) analysis and two-dimensional correlation spectroscopy (2D-COS). Sediment samples were collected from Baitapu River (BR) along gradients with human activities (e.g., rural, town, and urban sections) in Shenyang, northeast China, from which FA fractions were extracted and then determined via EEM fluorescence spectroscopy. According to optical indices, the autochthonous sources of sedimentary FA fractions in BR were more significant than the terrestrial sources. Among the sections, the contribution from autochthonous sources decreased in the following order: Rural &gt; Urban &gt; Town. Six components of sedimentary FA fractions were identified via EEM–PARAFAC: C1 comprised tryptophan-like (TRL) compounds; C2 was associated with microbial humic-like (MHL) compounds; C3, C4, and C5 were associated with FA-like (FAL) compounds; and C6 comprised humic acid-like (HAL) compounds. The proportion of sedimentary FA fractions decreased in the following order: MHL + FAL + HAL (humus, 77.37–88.90%) &gt; TRL (protein, 11.10–22.63%) for the three sections, showing that humus dominated. The town section exhibited the highest sedimentary FA fractions (5328.87 ± 1315.82 Raman unit [R.U.]), followed by the urban (4146.49 ± 535.75 R.U.) and rural (2510.56 ± 611.00 R.U.) sections. Three pollution sources were determined via principal component analysis (i.e., the dominant industrial source, domestic wastewater, and agricultural effluent). Additionally, the results from 2D-COS revealed that sedimentary FA fractions tended to stabilize as the protein-like component was transformed into the HAL component. Furthermore, we used the structural equation model to validate the critical environmental variables affecting the FA fraction transformation. The results can elucidate the influences of human activities on the dynamics of sedimentary FA fractions in urban rivers.

Integrating electrochemical pre-treatment with carrier-based membrane bioreactor for efficient treatment of municipal waste transfer stations leachate

An integrated process of electrochemical pre-treatment with carrier-based membrane bioreactor (MBR) was constructed for fresh leachate from waste transfer stations with high organic and NH4+-N content. Results showed that within a hydraulic retention time 40 h, the removal efficiencies of chemical oxygen demand (COD), NH4+-N, suspended solids (SS) and total phosphorus (TP) were over 98.5%, 91.2%, 98.3% and 98.4%, respectively, with the organic removal rate of 18.7 kg/m3. The effluent met the Grade A Standard of China (GB/T31962-2015). Pre-treatment contributed about 70 % of the degraded refractory organics and almost all the SS, with the transformation of the humic-like acid to readily biodegradable organics. Biotreatment further removed over 50% of nitrogen pollutants through simultaneous nitrification and denitrification (SND) and consumed about 30% of organics. Meanwhile, the addition of carriers in the oxic MBR enhanced the attached biomass and denitrification enzyme activity, alleviating membrane fouling.

Exogenous microbial antagonism affects the bioaugmentation of humus formation under different inoculation using Trichoderma reesei and Phanerochaete chrysosporium

This study was aimed at exploring the effect of antagonism of Trichoderma reesei (T.r) and Phanerochaete chrysosporium (P.c) on humification during fermentation of rice (RS) and canola straw (CS). Results showed that exogeneous fungi accelerated straw degradation and enzyme activities of CMCase, xylanase and LiP. P.c inhibited the activity of LiP when co-existing with T.r beginning, it promoted the degradation of lignin and further increased the production of humus-like substances (HLS) and humic-like acid (HLA) in later fermentation when nutrients were insufficient. The HLS of RTP was 54.9 g/kg RS, higher than the other treatments, and displayed more complex structure and higher thermostability. Brucella and Bacillus were the main HLA bacterial producers. P.c was the HLA fungal producer, while T.r assisted FLA and polyphenol transformation. Therefore, RTP was recommended to advance technologies converting crop straw into humus resources.

Component Properties and Heavy Metal Accumulation Characteristics of Contaminated Rice Straw Biochar During Oxygen-controlled Pyrolysis

Pyrolysis is an important technology to achieve the harmlessness and recycling of contaminated biomass. In this study, the effects of oxygen-controlled atmosphere on the component properties and heavy metal accumulation characteristics of contaminated rice straw biochar were studied. The results showed that low-oxygen pyrolysis could effectively produce biochar using contaminated rice straw and improve the stability of heavy metals in biochar. Under the nitrogen atmosphere, the yield of rice straw biochar was 29.4%-34.9%. The aromatization index (SUVA254) of dissolved organic matter (DOM) increased first and then decreased with the increase in pyrolysis temperature, whereas the fluorescent components were mainly humic-like acid substances. Meanwhile, Ca mainly existed in the form of CaCO3 in biochar. Compared with the pure nitrogen condition, the biochar yield was reduced by 5.6%-13.5% and 14.9%-15.7% under the pyrolysis atmosphere containing 10% and 20% oxygen content, respectively. Ca existed in the form of CaO in biochar, which increased the pH value of the biochar by more than 0.5 units. The oxygen of the pyrolysis atmosphere accelerated the degradation of the lignin component, resulting in the gradual decrease in SUVA254 of DOM. With the increase in oxygen content in the pyrolysis atmosphere, humic-like acid substances in DOM were transformed into fulvic-like acid substances. Under the conditions of 400℃ and a 10% oxygen-containing atmosphere, the exchangeable fractions of Cu, Cd, Pb, Ni, and As in biochar were decreased by 5.2%, 3.7%, 1.7%, 0.8%, and 0.7%, respectively, indicating that heavy metals are transformed into more stable states. The results suggested that the higher biochar yield and heavy metal stability could be obtained by introducing a proper amount of nitrogen into the air (controlling the oxygen content of approximately 10%) for pyrolysis treatment of contaminated rice straw, providing an economic and feasible technology for the achievement of harmlessness and recovery of contaminated rice straw.