Tinospora cordifolia Leaves Derived Carbon dots for Cancer Cell Bioimaging, Free radical Scavenging, and Fe3+ Sensing Applications.

Herein, we report the fabrication of Tinospora cordifolia leaves-derived carbon dots (TCLCDs) from aqueous extract of leaves as carbon source via simple, environmentally friendly, hydrothermal carbonization (HTC) technique. The synthesized TCLCDs were characterized for their physicochemical properties and further explored for in-vitro cancer cell bioimaging, radical scavenging, and metal ion sensing. The synthesized TCLCDs showed excitation-dependent emission property with maximum emission at 435 nm under the excitation of 350 nm. The High-Resolution Transmission Electron Microscopy (HRTEM) results revealed a roughly spherical shape with an average diameter of 5.47 nm. The diffused ring pattern of Selected Area Electron Diffraction (SAED) and halo diffraction pattern of X-ray diffraction (XRD) disclosed their amorphous nature. The Energy Dispersive X-ray (EDX) showed the existence of C, N, and O. The Fourier-transform infrared spectroscopy (FTIR) revealed the presence of -OH, -NH, -CN, and -CH groups. The TCLCDs showed excellent cellular biocompatibility with dose-dependent bioimaging results in melanoma (B16F10) and cervical cancer (SiHa) cell lines. Also, they exhibited excellent scavenging of free radicals with an IC50 value of 0.524 mg/mL & selective Fe3+ ion sensing with a detection limit of 0.414 µM. Further, they exerted excellent bacterial biocompatibility, photostability, and thermal stability. The overall results reflected their potential for in-vitro cancer cell bioimaging, free radical scavenging, and selective Fe3+ ion sensing.

High-performance size exclusion chromatography with online fluorescence and multi-wavelength absorbance detection for isolation of high-purity carbon dots fractions, free of non-fluorescent material.

The carbon dots (CDs) from natural nanographite oxide mixture (NGO-MIX) and from its fraction NGO (3.5-10K) recovered after ultrafiltration and dialysis were analyzed by 3D-excitation/emission matrix and high-performance size exclusion chromatography (HPSEC) combined with online fluorescence and absorbance detections. HPSEC chromatograms obtained simultaneously with absorption within the wavelength range 200-500 nm and fluorescence detection at λexc/λem = 270/450 nm/nm showed that NGO-MIX sample is not homogeneous and consist of well resolved CDs fractions with different sizes, absorption spectra and distinct fluorescence and non-fluorescence properties. Despite the twice higher fluorescence intensity of fraction NGO (3.5-10K) compared to the NGO-MIX, some impurity of non-fluorescent components was detected by HPSEC. The absorbance spectra of chromatographic peaks, extracted from the data of multi-wavelength absorbance detector, demonstrated different combinations of absorbance maxima. It means that different chromatographic peaks correspond to sized and chemically different CDs fractions. This study demonstrated for the first time the possibility of separating oxidized nanographite into homogeneous free from non-fluorescent material CDs fractions with their simultaneous spectroscopic characterization.

Carbon Dots for Efficient Small Interfering RNA Delivery and Gene Silencing in Plants.

The initiation of RNA interference (RNAi) by topically applied small interfering RNA has potential applications for plant functional genomics, crop improvement and crop protection, but the primary obstacle for the development of this technology is the efficient delivery of RNAi effectors into the cell. The plant cell wall is a particularly challenging barrier for the delivery of macromolecules because many of the transfection agents that are commonly used with animal cells produce nanocomplexes that are significantly larger than the size exclusion limit of the cell wall. Here, we illustrate the use of a class of very small nanoparticles, called carbon dots, for delivering small interfering RNA into the model plants Nicotiana benthamiana and tomato (Solanum lycopersicum). Low-pressure spray application of these formulations with a spreading surfactant resulted in strong silencing of GFP transgenes in both species. The delivery efficacy of carbon dot formulations was also demonstrated by the silencing of endogenous genes that encode two subunits of magnesium chelatase, an enzyme necessary for chlorophyll synthesis. The strong visible phenotypes observed with the carbon dot-facilitated delivery were validated by measuring significant reductions in the target gene transcript and/or protein levels. Methods for the delivery of RNAi effectors into plants, such as the carbon dot formulations described here, could become valuable tools for gene silencing in plants with practical applications in plant functional genomics and agriculture.

Alkaline thermal treatment of seaweed for high-purity hydrogen production with carbon capture and storage potential.

Current thermochemical methods to generate H2 include gasification and steam reforming of coal and natural gas, in which anthropogenic CO2 emission is inevitable. If biomass is used as a source of H2, the process can be considered carbon-neutral. Seaweeds are among the less studied types of biomass with great potential because they do not require freshwater. Unfortunately, reaction pathways to thermochemically convert salty and wet biomass into H2 are limited. In this study, a catalytic alkaline thermal treatment of brown seaweed is investigated to produce high purity H2 with substantially suppressed CO2 formation making the overall biomass conversion not only carbon-neutral but also potentially carbon-negative. High-purity 69.69 mmol-H2/(dry-ash-free)g-brown seaweed is produced with a conversion as high as 71%. The hydroxide is involved in both H2 production and in situ CO2 capture, while the Ni/ZrO2 catalyst enhanced the secondary H2 formation via steam methane reforming and water-gas shift reactions.

Efficient degradation of chloroquine drug by electro-Fenton oxidation: Effects of operating conditions and degradation mechanism.

In this work, the degradation of chloroquine (CLQ), an antiviral and antimalarial drug, using electro-Fenton oxidation was investigated. Due to the importance of hydrogen peroxide (H2O2) generation during electro-Fenton oxidation, effects of pH, current density, molecular oxygen (O2) flow rate, and anode material on H2O2 generation were evaluated. H2O2 generation was enhanced by increasing the current density up to 60 mA/cm2 and the O2 flow rate up to 80 mL/min at pH 3.0 and using carbon felt cathode and boron-doped diamond (BDD) anode. Electro-Fenton-BDD oxidation achieved the total CLQ depletion and 92% total organic carbon (TOC) removal. Electro-Fenton-BDD oxidation was more effective than electro-Fenton-Pt and anodic oxidation using Pt and BDD anodes. The efficiency of CLQ depletion by electro-Fenton-BDD oxidation raises by increasing the current density and Fe2+ dose; however it drops with the increase of pH and CLQ concentration. CLQ depletion follows a pseudo-first order kinetics in all the experiments. The identification of CLQ degradation intermediates by chromatography methods confirms the formation of 7-chloro-4-quinolinamine, oxamic, and oxalic acids. Quantitative amounts of chlorides, nitrates, and ammonium ions are released during electro-Fenton oxidation of CLQ. The high efficiency of electro-Fenton oxidation derives from the generation of hydroxyl radicals from the catalytic decomposition of H2O2 by Fe2+ in solution, and the electrogeneration of hydroxyl and sulfates radicals and other strong oxidants (persulfates) from the oxidation of the electrolyte at the surface BDD anode. Electro-Fenton oxidation has the potential to be an alternative method for treating wastewaters contaminated with CLQ and its derivatives.

Simultaneous nitrogen and carbon removal in a packed A/O reactor: effect of C/N ratio on microbial community structure.

In this research, a novel packed anoxic/oxic moving bed biofilm reactor (MBBR) was established to achieve high-organic matter removal rates, despite the carbon/nitrogen (C/N) ratio of 2.7-5.1 in the influent. Simultaneous nitrification-denitrification (SND) was investigated under a long sludge retention time of 104 days. The system exhibited excellent performance in pollutant removal, with chemical oxygen demand and total nitrogen (TN) enhanced to 93.6-97.4% and 34.4-60%, respectively. Under low C/N conditions, the nitrogen removal process of A/O MBBR system was mainly achieved by anaerobic denitrification. The increase of C/N ratio enhanced SND rate of the aerobic section, where dissolved oxygen was maintained at the range of 4-6 mg/L, and resulted in higher TN removal efficiency. The microbial composition and structures were analyzed utilizing the MiSeq Illumina sequencing technique. High-throughput pyrosequencing results indicated that the dominant microorganisms were Proteobacteria and Bacteroidetes at the phylum level, which contributes to the removal of organics matters. In the aerobic section, abundances of Nitrospirae (1.12-29.33%), Burkholderiales (2.15-21.38%), and Sphingobacteriales (2.92-11.67%) rose with increasing C/N ratio in the influent, this proved that SND did occur in the aerobic zone. As the C/N ratio of influent increased, the SND phenomenon in the aerobic zone of the system is the main mechanism for greatly improving the removal rate of TN in the aerobic section. The C/N ratio in the aerobic zone is not required to be high to exhibit good TN removal performance. When C/NH4+ and C/TN in the aerobic zone were higher than 2.29 and 1.77, respectively, TN removal efficiency was higher than 60%, which means that carbon sources added to the reactor could be saved. This study would be vital for a better understanding of microbial structures within a packed A/O MBBR and the development of cost-efficient strategies for the treatment of low C/N wastewater.

Selective inactivation of Gram-negative bacteria by carbon dots derived from natural biomass: Artemisia argyi leaves.

Infections caused by Gram-negative bacteria have been an increasing problem worldwide. Meanwhile, the overuse of traditional antibiotics has caused an emergence of drug resistance. The development of new antibacterial agents, which can cope with the threat from drug-resistant bacteria, is urgently needed. Herein, carbon dots (ACDs) derived from Artemisia argyi leaves were obtained via a smoking simulation method and exhibited selective antibacterial ability of targeting Gram-negative bacteria. The bactericidal efficiency of ACDs (150 µg mL-1) for Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa, and Proteusbacillus vulgaris) can reach 100%, while for Gram-positive bacteria (Staphylococcus aureus and Bacillus subtilis), ACDs have no significant antibacterial function, indicating that the particles can selectively target specific bacteria. The antibacterial mechanism for ACDs confirmed that ACDs could only damage the cell walls of Gram-negative bacteria but not that of Gram-positive bacteria. Moreover, ACDs can inhibit the activity of cell wall-related enzymes in Gram-negative bacteria by changing the enzymatic secondary structure. This work is of great significance for the development of new antibacterial nanomaterials derived from natural biomass as well as the treatment of infections caused by Gram-negative bacteria.

Electrochemical treatment of organic pollutants in landfill leachate using a three-dimensional electrode system.

The use of three-dimensional electrode is a new electrochemical oxidation technology for landfill leachate treatment. In this study, a particle electrode was developed using Fe/C granules, which were suspended between the cathode and the anode to create a three-dimensional electrode. The three-dimensional electrode activated sodium persulfate to treat landfill leachate. Fe/C granules were prepared by incorporating iron filings and hydrothermally carbonized biochar into alginate beads. The optimal parameters of the three-dimensional electrode for chemical oxygen demand (COD) removal from landfill leachate were determined based on a series of single factor experiments as an operating voltage of 5 V, a sodium persulfate concentration of 28 mM, and 1 g of Fe/C granules. Treatment with the three-dimensional electrode at optimized conditions achieved 72.9% removal of COD and 99.9% removal of ammonia nitrogen, resulting in landfill leachate being clear and transparent. The changes in total organic carbon, nitrite, and nitrate concentrations indicated that most organic pollution and ammonia nitrogen were converted into CO2 and N2. This study provides an alternative technology for the treatment of refractory organic pollutants.

Effect of pH on effluent organic matter removal in hybrid process of magnetic ion-exchange resin adsorption and ozonation.

It is essential to mitigate the risk of exposure to effluent organic matter (EfOM) in aquatic environments to ensure safe wastewater recycling. Magnetic ion-exchange (MIEX) resin adsorption combined with ozonation could provide EfOM removal. However, the poor understanding of the influences of the parameters and mechanisms in the hybrid process has restricted the applications. In this study, the response surface methodology was used to reveal the interactions of the major operation parameters. The degradation behaviour of the EfOM was investigated by using spectroscopy combined with mathematical methods. The effect of the pH on the EfOM removal was also analysed. The maximum efficiency of the removal of dissolved organic carbon (DOC) was 59.77% at the optimal MIEX resin dosage of 7.97 mL/L, ozone concentration of 8 mg/L, agitation speed of 199.84 r/min, and pH of 9.98. The ozonation was superior to resin adsorption in the removal of 1054-Da compounds, while the resin adsorption was advantageous in the removal of 4168-Da compounds. Three fluorescent components (C1, C2, and C3) were more easily subjected to external perturbation than the DOC and ultraviolet absorbance at 254 nm in the oxidation processes. The MIEX resin exhibited low efficiencies of removal of the fluorescent substances. A synchronous fluorescence analysis coupled with a two-dimensional correlation analysis revealed that the variation in EfOM followed the order of fulvic-to humic-like substances in the hybrid process of MIEX and the following ozonation. The pH was the most significant influencing factor in the hybrid process.

A simple way to improve a conventional A/O-MBR for high simultaneous carbon and nutrient removal from synthetic municipal wastewater.

In this study, two anoxic-oxic membrane bioreactor (A/O-MBR) systems, i.e. conventional and biofilm anoxic-oxic-membrane bioreactors (C-A/O-MBR and BF-A/O-MBR, respectively), were operated in parallel under conditions of complete sludge retention for the purposes of comparing system performance and microbial community composition. Moreover, with the microbial communities, comparisons were made between the adhesive stage and the suspended stage. High average removal of COD, NH4+-N and TN was achieved in both systems. However, TP removal efficiency was remarkably higher in BF-A/O-MBR when compared with C-A/O-MBR. TP mass balance analysis suggested that under complete sludge retention, polyurethane sponges that were added into the anoxic tank played a key role in both phosphorus release and accumulation. The qPCR analysis showed that sponge biomass could maintain a higher level of abundance of total bacteria than the suspended sludge. Meanwhile, AOB and denitrifiers were enriched in the suspended sludge but not in the sponge biomass. Results of illumina sequencing reveal that the compacted sponge in BF-A/O-MBR could promote the growth of bacteria involved in nutrient removal and reduce the amount of filamentous and bacterial growth that is related to membrane fouling in the suspended sludge.

New hexalactone derivatives and a pair of new oxaspiro-carbon epimeric glycosides from the fruits of Illicium lanceolatum.

Five new compounds (1-5), including three hexalactone derivatives (1-3) and a pair of new oxaspiro-carbon epimeric glycosides (4 and 5), and six known compounds (6-11) were obtained from the fruits of Illicium lanceolatum. The structures of the new compounds were elucidated using extensive spectroscopic data. The absolute configurations of compounds 1-3 were determined by an analysis of their CD spectra. It was determined that compounds 4 and 5, which are epimeric at C-5, possess the same 1-oxaspiro[4,5]decane-7α,8α,9ß-triol moiety. Plausible biogenetic pathways for 4 and 5 derived from the key precursor shikimic acid were proposed. Compounds 1-11 were all assayed on monosodium glutamate-induced human neuroblastoma SH-SY5Y cell damage. The results demonstrated that compounds 4, 5, and 8-10 possess potential neuroprotective effects. The anti-inflammatory, antiviral, and cytotoxic activities of 1-11 were also evaluated.

Combined chemically enhanced primary sedimentation and biofiltration process for low cost municipal wastewater treatment.

The main objective of wastewater treatment is to remove carbon and other nutrients from municipal and industrial effluents in order to protect the environment and human health. Typical wastewater treatment is usually achieved by a combination of physical, chemical and biological methods. In this work, municipal wastewater was depurated using chemically enhanced primary treatment (CEPT) in combination with a pilot-scale trickling filter. Lab scale experiments (Jar-tests) were carried out in order to determine the optimum dosage of chemicals. Selection criteria were the organic load removal efficiency and the low operational cost. Coagulation-flocculation process was conducted through polyaluminium chloride (PAC) and the cationic polyelectrolyte (Zetag 8180) addition. By combining CEPT and trickling filter, tCOD (total Chemical Oxygen Demand), sCOD (soluble Chemical Oxygen Demand), BOD5 (5-day Biochemical Oxygen Demand), NH4+-N, TSS (Total Suspended Solids), VSS (Volatile Suspended Solids) and PO43--P removal efficiencies were estimated to be 89, 82, 93, 60, 96, 96 and 78%, respectively. It is concluded that biological filtration contributed significantly in nutrients removal processes. Moreover, the obtained effluent was low in carbon and rich in nitrogen, which can be applied for restricted irrigation after disinfection, complying with the discharge limits set in the Greek Joint Ministerial Decree 145116/2011.

Decolorization and phytotoxicity reduction in an innovative anaerobic/aerobic photobioreactor treating textile wastewater.

The potential of a novel anaerobic/aerobic algal-bacterial photobioreactor for the treatment of synthetic textile wastewater (STWW) was here assessed. Algal-bacterial symbiosis supported total organic carbon, nitrogen and phosphorous removal efficiencies of 78 ±â€¯2%, 47 ±â€¯2% and 26 ±â€¯2%, respectively, at a hydraulic retention time (HRT) of 8 days. A decrease in the HRT from 8 to 4 and 2 days resulted in a slight decrease in organic carbon and phosphate removal, but a sharp decrease in nitrogen removal. Moreover, an efficient decolorization of 99 ±â€¯1% and 96 ±â€¯3% for disperse orange-3 and of disperse blue-1, respectively, was recorded. The effective STWW treatment supported by the anaerobic/aerobic algal-bacterial photobioreactor was confirmed by the reduction in wastewater toxicity towards Raphanus sativus seed germination and growth. These results highlighted the potential of this innovative algal-bacterial photobioreactor configuration for the treatment of textile wastewater and water reuse.

Comparison of monoculture and mixed culture (Scenedesmus obliquus and wild algae) for C, N, and P removal and lipid production.

This study compared the efficiency of nutrient removal and lipid accumulation by a monoculture of Scenedesmus obliquus and mixed cultures of microalgae. The highest removal efficiencies of ammonium (99.2%), phosphate (91.2%), and total organic carbon (83.6%) occurred in the monoculture. All the mixed cultures were dominated by S. quadricauda; in some mixed cultures, the proportions of Chlamydomonas reinhardtii and C. microsphaera reached > 20%. The lipid content and lipid production in the monoculture were 15.9% and 52.3 mg kg-1, respectively, significantly higher than those in all the mixed cultures of microalgae. In all the mixed cultures, the proportion of palmitic acid was > 50%. The results suggest that the monoculture had advantages over the mixed culture of microalgae in terms of nutrient removal and lipid production.

Hydrochars produced with by-products from the sucroenergetic industry: a study of extractor solutions on nutrient and organic carbon release.

Hydrothermal carbonization transforms biomass into value-added material called hydrochar. The release of nutrients (P, N, Ca, Mg, and K) and organic carbon (TOC) from hydrochar in different extractive solutions was investigated in this study. Two sets of hydrochar were produced: (i) hydrochar prepared from sugarcane bagasse and vinasse mixture (BV-HC) and (ii) hydrochar prepared by the addition of H3PO4 to this mixture (BVA-HC). Both hydrochar types released significative amounts of nutrient and organic carbon, mainly Ca (5.0 mg g-1) in the mixture (KCl, K2SO4, NaOH, 1:1:1) extractive solution and TOC (72.6 mg g-1) in the NaOH extractive solution, for BV-HC. Nutrient release was influenced by pH and ionic strength. The release of P, Ca, and Mg was affected by the presence of insoluble phosphate phases in BVA-HC. The release of nutrients P, N, Ca, Mg, and K and organic carbon demonstrated that hydrochar has potential for soil application purposes.

Nitrogen Removal in Oligotrophic Reservoir Water by a Mixed Aerobic Denitrifying Consortium: Influencing Factors and Immobilization Effects.

Nitrogen pollution in reservoirs has received increasing attention in recent years. Although a number of aerobic denitrifying strains have been isolated to remove nitrogen from eutrophic waters, the situation in oligotrophic water environments has not received significant attention. In this study, a mixed aerobic denitrifying consortium screened from reservoir samples was used to remove nitrogen in an oligotrophic denitrification medium and actual oligotrophic source water. The results showed that the consortium removed 75.32% of nitrate (NO3--N) and 63.11% of the total nitrogen (TN) in oligotrophic reservoir water during a 24-h aerobic cultivation. More initial carbon source was helpful for simultaneous removal of carbon and nitrogen in the reservoir source water. NO3--N and TN were still reduced by 60.93% and 46.56% at a lower temperature (10 °C), respectively, though the rates were reduced. Moreover, adding phosphorus promoted bacterial growth and increased TN removal efficiency by around 20%. The performance of the immobilized consortium in source water was also explored. After 6 days of immobilization, approximately 25% of TN in the source water could be removed by the carriers, and the effects could last for at least 9 cycles of reuse. These results provide a good reference for the use of aerobic denitrifiers in oligotrophic reservoirs.

Potential of the integration of coagulation and ozonation as a pretreatment of reverse osmosis concentrate from coal gasification wastewater reclamation.

Combination of coagulation and ozonation was used to treat brine derived from a three-stage reverse osmosis (RO) process during coal gasification wastewater reclamation. Effects of operating parameters on the removals of total organic carbon (TOC), color and UV absorbance at 254 nm (A254) were investigated during coagulation and ozonation. All the removal efficiencies of TOC, A254 and color of FeCl3 coagulant are about twice those of AlCl3 coagulant at the same molar dose since almost all the molecular weight fractions of RO concentrate (ROC) could be removed effectively by FeCl3 coagulant while only the fractions of molecular weight > 3 k Da could be removed effectively by AlCl3 coagulant. The TOC removal increases with the increasing of ozone dose and reaction temperature during ozonation of ROC after coagulation pretreatment. TOC and color of ROC after pretreated by coagulation could be further removed effectively during ozonation since ozonation can significant reduce the fluorescence response of all the fractions of effluent organic matter in ROC. It is unexpectedly found that the increase of A254 is observed after ozonation, this is because the intensity of absorbance at 254 nm by the low molecular weight transformation products (<2 k Da) increases significantly with the reaction time after 30 min. The coagulation coupling with ozonation is efficient in the removals of both TOC and color of ROC.

Wastewater treatment in amine-based carbon capture.

Amine-based CO2 capture (ACC) has become one cost-effective method for reducing carbon emissions in order to mitigate climate changes. The amine-rich wastewater (ARWW) generated from ACC may contain a series of degradation products of amine-based solvents (ABSs). These products are harmful for ecological environment and human health. Effective and reliable ARWW treatment methods are highly required for mitigating the harmfulness. However, there is a lack of a comprehensive review of the existing limited methods that can guide ARWW-related technological advancements and treatment practices. To fill this gap, the review is achieved in this study. All available technologies for treating the ARWW from washwater, condenser, and reclaimer units in ACC are examined based on clarification of degradation mechanisms and ARWW compounds. A series of significant findings and recommendations are revealed through this review. For instance, ARWW treatment methods should be selected according to degradation conditions and pollution concentrations. UV light can be only used for treating wastewater from washwater and condenser units in ACC. Biological activated carbon is feasible for removing nitrosamines from washwater and condenser units. Sequence batch reactors, microbial fuel cells, and the other techniques for removing amines and similar degradation products are applicable for treating ARWW. This review provides scientific support for the selection and improvement of ARWW treatment techniques, the mitigation of ACC's consequences in environment, health and other aspects, and the extensive development and applications of ACC systems.

[Nitrite Accumulation Characteristics of Partial Denitrification in Different Sludge Sources Using Sodium Acetate as Carbon Source].

In order to explore the characteristics of nitrite accumulation during the operational period of partial denitrification in different sludge sources using sodium acetate as a carbon source, No.1 SBR and No.2 SBR were used to inoculate with surplus sludge taken separately from a secondary sedimentation tank of a sewage treatment plant and simultaneous nitrification and denitrifying phosphorus removal system. By reasonably controlling the initial nitrate concentration and anoxic time, partial denitrification was realized. The carbon and nitrogen removal characteristics under different initial COD and NO3--N concentrations were investigated. The results showed that, using sodium acetate as the carbon source, the partial denitrification process in No.1 SBR and No.2 SBR sludge successfully began in 21 d and 20 d, respectively. The accumulation of NO2--N and nitrite accumulation rate (NAR) in reactors were maintained at high levels (12.61 mg·L-1, 79.76% and 13.85 mg·L-1, 87.60%, respectively). When the initial NO3--N concentration of No.2 SBR was 20 mg·L-1 and the initial COD concentration increased from 60 mg·L-1 to 140 mg·L-1, the operation time for achieving the highest NO2--N accumulation in the system was shortened from 160 min to 6 min. The NO3--N ratio of the denitrification rate (in VSS) increased from 3.84 mg·(g·h)-1 to 7.35 mg·(g·h)-1. Increased initial COD concentration was beneficial to the accumulation of NO2--N during partial denitrification. When the initial COD concentration of No.2 SBR was 100 mg·L-1 and the initial NO3--N concentration increased from 20 mg·L-1 to 30 mg·L-1, NAR was maintained above 90% and up to 100% (the initial NO3--N concentration was 25 mg·L-1). When the initial NO3--N concentration was ≥ 35 mg·L-1, insufficient COD caused NO3--N to be completely reduced to NO2--N. Under different initial COD concentrations (80, 100, or 120 mg·L-1) and different initial NO3--N concentrations (20, 25, 30, or 40 mg·L-1), the nitrogen and carbon removal and partial denitrification performance of the No.2 SBR was better than that of No.1 SBR.

[Carbon and Nitrogen Removal Characteristics of ABR Decarbonization-CANON Coupling Process].

If municipal wastewater can be treated by the completely autotrophic nitrogen removal over nitrite (CANON) process, it will greatly reduce the energy consumption of municipal wastewater treatment. The CANON reactor with a fiber carrier was started up by seeding nitrosation sludge and anaerobic ammonia oxidation (ANAMMOX) sludge in the continuously stirred tank reactor (CSTR). An ABR decarbonization system was added to the front of the CANON system to build the ABR decarbonization-CANON coupling process to examine carbon and nitrogen removal characteristics of the whole system. The high throughput sequencing technology of MiSeq was also employed to analyze the structure of the microbial community before and after the reactivation. The results showed that mixing nitrosation sludge and ANAMMOX sludge in the CSTR reactor under controlled parameters (DO of 0.5-2 mg·L-1; HRT for 6 h; pH of 8) allowed the CANON system to successfully start within 55 d, with a TN removal rate of 81%-87% and ammonia nitrogen load of 0.195 kg·(m3·d)-1. The effluent COD concentration of the ABR decarbonizing system did not adversely affect the subsequent CANON system, and the TN removal rate of the ABR decarbonization-CANON process was between 74% and 87%. Additionally, the average concentration of COD in the effluent was 40 mg·L-1. At the same time, the Proteobacteria gate significantly improved after the CANON system began, and the proportion of Sphingobacteria decreased to 6.8%. Nitrifying bacteria and anaerobic ammonia oxidizing bacteria in the CANON system continuously eliminated the inferior bacterial groups to become the dominant group in the reactor. The integrated ABR decarbonization-CANON process had a positive effect on the denitrification and decarbonization of urban sewage.