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Alkaline pre-treatment is known to enhance the acid production efficiency of sludge but adversely affects its dewatering performance. In this study, the improvement of sludge dewaterability by a novel bioleaching system with inoculating domesticated acidified sludge (AS) and its underlying mechanism were investigated. The results showed that although the addition of Fe2+ and the reduction of pH improved the dewatering performance of sludge, their effects were inferior to that of AS + Fe. The addition of AS and Fe2+ significantly reduced the specific resistance to filtration and capillary suction time of the sludge by 98.6 % and 95.5 %, respectively. This improvement in dewatering performance was achieved through the combined actions of bio-acidification, bio-oxidation, and bio-flocculation. Remarkably, under alkaline pH, microorganisms in AS remained active, leading to the formation of iron-based bioflocculants, along with a rapid pH decrease. These bioflocculants, in combination with protein (PN) in tightly bound extracellular polymeric substances (TB-EPS) through amide bonding, transformed TB-EPS from extractable to non-extractable form, reducing PN content from 12.1 mg g-1DS to 5.09 mg g-1DS and altering the protein's secondary structure. Consequently, the gel-like TB-EPS matrix effectively broke down, releasing cellular water and significantly enhancing sludge dewaterability.
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Esgotos , Água , Água/química , Ferro/química , Filtração , Oxirredução , Eliminação de Resíduos Líquidos/métodosRESUMO
Bioleaching and Fenton technology are commonly used preconditioning techniques for sludge dewatering. This study compared the dewatering mechanisms of different conditioning technologies. The results showed that bound water, specific resistance to filtration (SRF), and capillary suction time decreased from 3.95 g/g, 6.16 × 1012 m/kg, and 130.6 s to 3.15 g/g, 2.81 × 1011 m/kg, and 33 s, respectively, under combined treatment condition. Moreover, the free radicals, including ·OH, O2-·and Fe (â £), further damaged the cell structure, thus increasing the concentration of DNA in the S-EPS layer. This intense degradation sludge particle size decreased by 15.6% and significantly increased zeta potential. Under the combined technology, the α-helix and ß-sheet decreased by 42.2% and 56.5%, respectively, destabilizing the spatial structure of proteins and promoting the release of bound water. In addition, the combined technology decreased (Ala/Lys) ratio in the TB-EPS layer by 67.6%, indicating the weakening of protein water-holding capacity. Moreover, the conversion of oxygen-containing compounds to nonpolar hydrocarbons increased the hydrophobicity of the sludge under a combined treatment, thus enhancing dewatering performance.
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Interações Hidrofóbicas e Hidrofílicas , Esgotos , Esgotos/química , Eliminação de Resíduos Líquidos/métodos , Tamanho da Partícula , Ferro/química , Filtração , Água/químicaRESUMO
Simultaneous bio-treatment processes of organic carbon (C)-, nitrogen (N)-, and phosphorus (P)-containing wastewater are challenged by insufficient carbon sources in the effluent. In the present study, two parallel anaerobic/aerobic sequencing batch reactors (R-1 and R-2) treating low C/N (≤4) wastewater were employed using different partial nitrification start-up strategies, controlled reduced aeration, and decreased sludge retention time. Advanced removal efficiencies for NH4+-N (≥96%), total nitrogen (TN, ≥86%), PO43--P (≥95%), and CODintra (≥91%) were realized, with TN and PO43--P effluent concentrations of 10.0 ± 3.5 and 0.11 ± 0.3 mg/L in R-1 and 9.28 ± 4.0 and 0.11 ± 0.1 mg/L in R-2, respectively. Higher nitrite accumulation rate (nearly 100%) and TN (121.1 ± 0.7 mg TN/g VSS·d) and P (12.5 ± 0.6 mg PO43--P/g VSS·d) removal loadings were obtained in R-2 by a thorough elimination of nitrite-oxidizing bacteria. Moreover, different microbial structures and nutrient removal pathways were identified. Denitrifying glycogen-accumulating organisms (Candidatus Competibacter) and phosphorus-accumulating organisms (PAOs) (Tetrasphaera) removed N and P with partial nitrification-endogenous denitrification pathways and aerobic P removal in R-1. In R-2, aerobic denitrifying bacteria (Psychrobacter) and PAOs ensured N and P removal through the partial nitrification-aerobic denitrification and aerobic P removal pathways. Compared to R-1, R-2 offers greater efficiency, convenience, and scope to further reduce carbon-source demand.
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Esgotos , Águas Residuárias , Desnitrificação , Nitrificação , Nitritos , Carbono , Nitrogênio , FósforoRESUMO
Two Wells-Dawson arsenotungstate coordination polymers, [{CuII(bim)2}3(As2W18O62)] (1) and [(CuI10pz10Cl4)(As2W18O62)] (bim = 2,2'-biimidazole; pz = pyrazine), have been assembled via a hydrothermal method and fully characterized. Compound 1 exhibits a 2,6-connected two-dimensional hybrid layer based on asymmetrically modified {As2W18} anions and {Cu(bim)2} linkers, which is extended to a three-dimensional network with a special interlayer structure and a one-dimensional tunnel. Compound 2 is a host-guest framework that consists of a Cu-pz-Cl network with 20-member square rings, 16-member irregular rings, and embedded eight-node {As2W18} guest molecules. Compounds 1 and 2 show uncommon specific capacitance (834.8 and 960.1 F g-1, respectively, at a current density of 2.4 A g-1), enduring cycling stability (capacitance retention rates of 89.3% and 91.9%, respectively, after 5000 cycles), and good electrical conductivity, which are superior to those of the unmodified zero-dimensional Dawson arsenotungstate compound and most reported electrode materials in terms of their stable structure, special layer spacing, and orderly channels. Moreover, the title compounds exhibit excellent electrocatalytic activity for oxidizing ascorbic acid and reducing nitrite.
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Different metal-organic units were introduced into the {PMo12} polyoxometalate (POM) system to yield three porous coordination polymers with distinct characteristics, {Cu(pra)2}[{Cu(pra)2}3{PMo11VIMoVO40}] (1), [{Ag5(pz)6(H2O)0.5Cl}{PMo11VIMoVO40}] (2), and [{Cu3(bpz)5(H2O)}{PMo12O40}] (3) (pra = pyrazole; pz = pyrazine; bpz = benzopyrazine), via an in situ hydrothermal method. In comparison with the maternal Keggin cluster and most reported POM electrode materials, compounds 1-3 exhibit larger specific capacitances (672.2, 782.1, and 765.2 F g-1 at a current density of 2.4 A g-1, respectively), superior cyclic stability (91.5%, 89.3%, and 87.8% of cycle efficiency after 5000 cycles, respectively), and boosted conductivity, which may be attributed to the introduction of metal-organic units. The result indicates that metal-organic units can effectively enhance the capacitance performance of POMs. This may be due to the fact that they provide additional redox centers, induce the formation of stable porous structures, and improve ion/electron transfer efficiency. Compounds 1-3 present excellent electrocatalytic activity in reducing peroxide (H2O2) and oxidizing ascorbic acid (AA). In addition, compound 2 shows an outstanding sensing performance detection of AA and H2O2.
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Different transition metal (TM) units are introduced into a trivacant Keggin cluster to form three sandwich polytungstate derivatives, (H2en)[{K(H2O)0.5}2{K2(H2O)3}{Ni(H2O)(en)2}2{Ni4(H2O)2(PW9O34)2}] (1), [Cu6(Himi)6{AsIIIW9O33}2]·5H2O (2), and (H2btp)4[FeIII2FeII2(H2O)2(AsW9 O34)2]·4H2O (3) (en = ethanediamine; imi = imidazole; btp = 1,3-bis(1, 2, 4-triazol-1-yl) propane). Compound 1 is a 2,3,8-connected 3D network with {43}2{46·66·83·612·8}{6}2 topology based on bisupported tetra-Ni sandwich phosphotungstate and two kinds of potassium connection units. Compound 2 is a dense 12-connected 3D supramolecular network with {324·436·56} topology based on hexa-Cu(imi) sandwiched arsenotungstate. Compound 3 represents the first mixed valence tetra-Fe substituted sandwich arsenotungstate assembly. Compounds 1-3 show enhanced supercapacitor performance (618.2, 603.4, and 504.6 F·g-1 at a current density of 2.4 A·g-1 with 91.5%, 89.3%, and 87.8% of cycle efficiency after 5000 cycles, respectively) compared to their maternal polyoxometalates (POMs) and most reported POM-based electrode materials, which suggests that the introduction of multinuclear TM into vacant POMs is an effective method to improve the energy storage performance of POMs. In addition, compounds 1 and 3 exhibit dual-functional electrocatalytic behaviors in the reduction of iodate and the oxidation of dopamine for introduction of {Ni4} and {Fe4} units.
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The mixed hexa-transition metal (hexa-TM) sandwiched arsenotungstate derivative, [CuI3(pz)2(phen)3]2[CuI(phen)2][{Na(H2O)2}{(VIV5CuIIO6)(AsIIIW9O33)2}]·6H2O (1) (pz = pyrazine; phen = 1,10-phenanthroline), has been hydrothermally synthesized and structurally characterized. In compound 1, two {AsW9O33} clusters are connected by mixed hexa-TM ring unit {VVI5CuIIO6} to form a sandwich-type dimer, which are further bonded in "ABAB" mode by the {Na(H2O)2} linker resulting in pure inorganic chains. The unique "L-shaped" trinuclear complex {Cu3(phen)3(pz)2} is supported together via staggered π-π interactions to generate extending waveform two-dimensional supramolecular layers, which are further aggregated with their adjacent analogues by complexes {Cu(phen)2} via H-bonding interaction to yield an unprecedented three-dimensional (3D) metal-organic networks with one-dimensional (1D) cavities. The pure inorganic 1D sandwich chains are implanted in the cavities as guest units via supramolecular interactions to form a POMOF 3D framework. Compound 1, as the electrode of the supercapacitor, exhibits higher specific capacitances (825 F g-1 at a current density of 2.4 A g-1), better rate capability, more durable cyclic stability (91.4% of cycle efficiency after 3000 cycles), and improved conductivity and electroactivity compared to those of parent polyoxometalate (POM) Na9[AsW9O33]·19H2O (2) and 6-Cu-substituted POM [Cu6(imi)6{AsIIIW9O30Cl3}2]·6H2O (3), which may be attributed to the introduction of V4+, the unique host-guest structure, and the rich π electron system. In addition, compound 1 exhibits dual-function electrocatalytic behavior in reducing inorganic salt IO3- and oxidizing the organic molecule dopamine.
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Four basket-like organic-inorganic hybrids, formulated as [{Cu(II)(H2O)2}{Ca4(H2O)4(HO0.5)3(en)2}{CaâP6Mo4(V)Mo14(VI)O73}]·7H2O (1), (H4bth)[{Fe(II)(H2O)}{CaâP6Mo18(VI)O73}]·4H2O (2), (H2bih)3[{Cu(II)(H2O)2}{CaâP6Mo2(V)Mo16(VI)O73}]·2H2O (3), (H2bib)3[{Fe(II)(H2O)2}{CaâP6Mo2(V) Mo16(VI)O73}]·4H2O (4), (bth = 1,6-bis(triazole)hexane; bih = 1,6-bis(imidazol)hexane; bib = 1,4-bis(imidazole)butane) have been hydrothermally synthesized and fully characterized. Compounds 1-4 contain polyoxoanion [CaâP6Mon(V)Mo18-n(VI)O73]((6+n)-) (n = 0, 2, or 4) (abbreviated as {P6Mo18O73}) as a basic building block, which is composed of a "basket body" {P2Mo14} unit and a "handle"-liked {P4Mo4} fragment encasing an alkaline-earth metal Ca(2+) cation in the cage. Compound 1 exhibits an infrequent 2D layer structure linked by the Cu(H2O)2 linker and an uncommon tetranuclear calcium complex, while compound 2 is 8-connected 2-D layers connected by binuclear {Fe2(H2O)3} segaments, which are observed for the first time as 2-D basket-like assemblies. Compounds 3 and 4 are similar 1D Z-typed chains bonded by M(H2O)2 units (M = Cu for 3 and Fe for 4). The optical band gaps of 1-4 reveal their semiconductive natures. They exhibit universal highly efficient degradation ability for typical dyes such as methylene blue, methyl orange, and rhodamine B under UV light. The lifetime and catalysis mechanism of the catalysts have been investigated. The compounds also show good bifunctional electrocatalytic behavior for oxidation of amino acids and reduction of NO2(-).
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Cálcio/química , Imidazóis/química , Molibdênio/química , Compostos Organometálicos/química , Triazóis/química , Butanos/química , Catálise , Cobre/química , Cristalografia por Raios X , Compostos Ferrosos/química , Hexanos/química , Modelos Moleculares , Compostos Organofosforados/química , FotóliseRESUMO
Polyoxometalate-based metal-organic frameworks (POMOFs) have received wide attention in supercapacitors and H2O2 detection due to their possession of the rich redox active sites of polyoxometalates (POMs) and the ordered structure of metal-organic frameworks (MOFs). In this study, we successfully synthesized a host-guest Cu3[P2W18O62]@HKUST-1 (HRBNU-7) compound by a grinding method. Cu3[P2W18O62] successfully entered the HKUST-1 pores as confirmed by the results of infrared (IR) spectroscopy, powder X-ray diffraction (PXRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The specific capacitance of HRBNU-7 is 318.6 F g-1 at 1 A g-1 in a three-electrode system using nickel foam as the collector. The specific capacity retention is 92.36% after 5000 cycles. The assembled symmetrical supercapacitor (SSC) achieved a high energy density of 10.58 W h kg-1 at a power density of 500.00 W kg-1. In addition, HRBNU-7 exhibits excellent electrochemical detection of H2O2, including a wide linear range of 0.5 µM-0.3 mM, a low detection limit of 0.17 µM, and excellent selectivity and stability, and it can be effectively utilized for the analysis of H2O2 content in actual serum samples. These excellent properties are attributed to the unique redox activity of Cu3[P2W18O62] and the high specific surface area of HKUST-1. This work offers a strategy for exploring POMOFs as electrode materials in supercapacitors and electrochemical sensors.
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The effects of the addition of EDTA-2Na on sludge disintegration and phosphorus (P) migration during anaerobic fermentation (AF) of waste activated sludge (WAS) are investigated. The efficiency of sludge disintegration was positively correlated with the dose of EDTA-2Na from 0.5-2.0â g/g SS, and an enormous quantity of P was liberated into the aqueous phase, accompanied by sludge disintegration. The proper dose of EDTA-2Na for P release from WAS was 1.5â g/g SS, with an orthophosphate concentration of 394.72â mg/L. P release was more consistent with the pseudo second-order kinetic model. The migration of P species during AF with EDTA-2Na addition was also studied. Orthophosphate was the main species in both of the liquid phase and the loosely bound extracellular polymeric substances (EPS), but organic P (OP) was much more abundant in tightly bound EPS. Inorganic P (IP) was the dominant P speciation in the solid and was mainly distributed in the fraction of non-apatite IP, which accounted for more than 62.8% of IP in the presence of EDTA-2Na. In addition, both IP and OP in the solid contributed to the accumulation of P and the former was outperformed. Furthermore, the increased total dissolved P mainly came from cells. However, the fermented sludge tended to be smaller and to have low compressibility, which is detrimental to its further treatment.
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Fósforo , Esgotos , Fermentação , Anaerobiose , Ácido Edético , Fosfatos , Eliminação de Resíduos LíquidosRESUMO
Designing and preparing dual-functional Dawson-type polyoxometalate-based metal-organic framework (POMOF) energy storage materials is challenging. Here, the Dawson-type POMOF nanomaterial with the molecular formula CoK4[P2W18O62]@Co3(btc)2 (abbreviated as {P2W18}@Co-BTC, H3btc = 1,3,5-benzylcarboxylic acid) was prepared using a solid-phase grinding method. XRD, SEM, TEM et al. analyses prove that this nanomaterial has a core-shell structure of Co-BTC wrapping around the {P2W18}. In the three-electrode system, it was found that {P2W18}@Co-BTC has the best supercapacitance performance, with a specific capacitance of 490.7 F g-1 (1 A g-1) and good stability, compared to nanomaterials synthesized with different feedstock ratios and two precursors. In the symmetrical double-electrode system, both the power density (800.00 W kg-1) and the energy density (11.36 Wh kg-1) are greater. In addition, as the electrode material for the H2O2 sensor, {P2W18}@Co-BTC also exhibits a better H2O2-sensing performance, such as a wide linear range (1.9 µM-1.67 mM), low detection limit (0.633 µM), high selectivity, stability (92.4%) and high recovery for the detection of H2O2 in human serum samples. This study provides a new strategy for the development of Dawson-type POMOF nanomaterial compounds.
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Improving the dewatering performance of sewage sludge is of great scientific and engineering significance in the context of accelerated urbanization and increasingly strict environmental regulations. Acidified sludge (AS) can improve sludge dewatering performance, but the dewatering effect of repeated inoculation is unclear. The effects of long-term repeated inoculation of AS on the sludge dewaterability were investigated. The molecular structure and microbial community succession of extracellular polymeric substances (EPS) are emphasized. The results revealed that increasing the inoculation ratio of AS reduced the pH, absolute value of sludge zeta potential, and sludge particle size, and the decreasing trend was more evident with prolonging treatment time. Under the conditions of 30% and 50% AS inoculation, the dewatering performance of the sludge was significantly improved (p < 0.05). Compared with the raw sludge, the specific resistance of filtration (SRF) and capillary suction time of 30% inoculation were reduced by 64.3% and 50.1% after 30 cycles, respectively. Excluding loosely bound (LB)-EPS, soluble (S)-EPS and tightly bound (TB)-EPS exhibited a visible decrease, the protein in TB-EPS was significantly related to sludge dewaterability (p < 0.05). The fluorescent components of aromatic protein and fulvic acid-like substances in TB-EPS were significantly associated with SRF, with a correlation coefficient 0.99 (p < 0.05). Both the increase in the percentages of random coil and decrease in α-helix in TB-EPS contributed to improving dewaterability. Increasing Firmicutes and decreasing Chloroflexi levels improved the sludge dewatering capacity. Repeated inoculation did not disrupt the dewatering effect of AS rather increased the feasibility of the engineering application of AS. Considering the dewatering performance and cost synthetically, 30% AS inoculated ratio is feasible for practical applications.
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Matriz Extracelular de Substâncias Poliméricas , Esgotos , Esgotos/química , Estrutura Molecular , Água/química , Proteínas/química , Eliminação de Resíduos Líquidos/métodosRESUMO
Creating inorganic-organic hybrids with polyoxometalates (POMs) and metal-organic frameworks (MOFs) as energy storage and dye-degradation materials remains challenging. Here, a new hybrid nanomaterial Mn-BTC@Ag5[BW12O40] is synthesized by using Ag5[BW12O40] and Mn3(BTC)2(H2O)6 (Mn-BTC, BTC = 1,3,5-benzenetricarboxylic acid) through a plain grinding method. The structure and morphology characterization by scanning electron microscopy (SEM), powder X-ray diffraction (XRD), and transmission electron microscopy (TEM) shows that the synthetic products have core-shell construction. Due to its unique structure wherein the core is Mn-BTC and the shell is Ag5[BW12O40], it exhibits excellent capacitance performance. In a three-electrode system where nickel foam is a collector, at a current density of 1 A g-1, its specific capacitance is 198.09 F g-1; after 5000 cycles, the capacitance retention rate is 94.4%. When the power density is 503.1 W kg-1, the symmetrical supercapacitor reveals a high energy density which is 10.9 W h kg-1. At the same time, the capacitance retention is 92.9% after 5000 cycles which showed good cycle stability. The photocatalytic degradation efficiencies of rhodamine B (RhB), methyl orange (MO) and methylene blue (MB) dyes exceed 90% after 140 min, and the degradation results remained unchanged after five photocatalytic cycles. The photocatalytic degradation mechanism shows that ËOH has a major effect. The results show that this research provides a fresh idea for the development of energy storage and dye photocatalytic degradation materials.
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Persulphates, an advanced oxidation process, has been recently used as an alternative pretreatment method to enhance short-chain fatty acids (SCFAs) yield from waste-activated sludge (WAS) anaerobic fermentation (AF). But so far, the effects of peroxydisulphate (PDS) dosages on mesophilic anaerobic fermentation are still not studied fully. Herein, we explored the influences of potassium PDS addition on mesophilic AF of WAS. Notably, the addition of PDS could drastically accelerate WAS solubilization and hydrolysis, which was proportional to the amount of PDS. The maximal total SCFAs yield of 249.14â mg chemical oxygen demand/L was obtained with 120â mg PDS/g suspended solids addition at 6 days of AF, which was 2.2-fold that of the control one. Tightly bound extracellular polymeric substances (EPSs) were transformed into loosely bound EPS and dissolved organic matters, and aromatic proteins and humic-like substances of EPSs were disintegrated, which were caused by the devastating effects of PDS treatments on EPSs disruption. The intracellular constituents of microbial cells in the sludge were released accordingly. As a result, there was release of soluble substrates derived from the disintegration of both EPSs and cells, the amounts of which were proportional to the dose of PDS. Moreover, microbial diversity and richness were both decreased in the presence of PDS, and the relative abundance of phyla Actinobacteria increased with the increase of the PDS dosage. In addition, the stability of sludge flocs was destroyed in the presence of PDS, the distribution of particle size tended to be small and dispersive, and dewaterability of the sludge was deteriorated.
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Ácidos Graxos Voláteis , Esgotos , Anaerobiose , Fermentação , Compostos de Potássio , Esgotos/química , SulfatosRESUMO
Because of the increasingly widespread contamination of antibiotics, the preparation of biochar by heteroatom doping to further improve the catalytic degradation efficiency of antibiotics has become a major focus of research. In this study, N-doped (NBC), S-doped (SBC), and NS-doped (NSBC) moso bamboo biochar were obtained at preparation temperatures of 300-700 °C. The concentration of environmentally persistent free radicals (EPFRs) in all biochars peaked when the preparation temperature was 500 °C: 2.45 × 1019 spins·g-1 (BC), 9.23 × 1019 spins·g-1 (NBC), 6.10 × 1019 spins·g-1 (SBC), and 4.36 × 1019 spins·g-1 (NSBC). After heteroatom doping, EPFR species were more abundant, and the distribution of three types of EPFRs (oxygen-centered (g > 2.0040), carbon-centered (g < 2.0030), and carbon-centered radicals with oxygen atom free radicals (2.0030 < g < 2.0040) varied with the preparation temperature. In the process of antibiotic degradation, both NBC and SBC increased the degradation rate of antibiotics, whereas NSBC reduced the degradation rate. Compared with the degradation rate of antibiotics of biochar (79.86%), the degradation rate of antibiotics by NBC, SBC, and NSBC via PMS activation was 92.23%, 88.86%, and 70.97% on average in 30 min, respectively. The greatest contributors to the catalytic degradation were SO4â¢-, followed by 1O2, â¢OH, and O2â¢-. EPFRs and 1O2 might be the main contributors to the free radical and non-free radical pathways. The enhancement of EPFRs following the N doping or S doping of biochar is the key factor underlying PMS activation. Therefore, changes in the structure of biochar can better activate PMS to produce reactive oxygen species-degrading antibiotics. The mineralization rate of antibiotics by BC, NBC, SBC, and NSBC was 42.12%, 47.06%, 44.99%, and 39.01%, respectively. This means that a small portion of the antibiotics was completely decomposed into CO2, H2O, and inorganic substances after degradation. Cyclic experiments showed that heteroatom-doped biochar had higher reusability, and the degradation rate decreased less than 15%.
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Carvão Vegetal , Sasa , Antibacterianos , Carvão Vegetal/química , Radicais Livres/química , Nitrogênio , Pirólise , Enxofre , TemperaturaRESUMO
An efficient strategy for short-chain fatty acid (SCFA) production from sludge anaerobic fermentation was proposed with the combination of yeast and alkyl polyglucose (APG). It revealed that the synergetic effect of yeast and APG could boost the SCFA concentration to the maximum value of 2800.34 mg COD/L within 9 days at 0.20 g/g suspended solids (SS) yeast and 0.20 g/g SS APG, which was significantly higher than that of its counterparts. Interestingly, the sludge solubilization, the biodegradability of fermentation substrate, as well as the acidification of hydrolyzed products, was evidently improved in the coexistence of APG and yeast. The activities of hydrolytic enzymes and acetate kinase were also stimulated, whereas the coenzyme F420 was inhibited. The synergetic effect of yeast and APG used in this work enriches the study of carbon resource recovery from sludge anaerobic fermentation.
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{P6Mo18} poly(oxometalate) (POM) clusters have huge steric hindrance and limited active oxygen atoms, which make them difficult to combine with metal-organic units to form three-dimensional (3D) porous structures. Therefore, functionalization of such POMs has always been a bottleneck that is difficult to break through. In this study, {P6Mo18} POM was successfully grafted on a lock-like metal-organic chain to generate a multiporous coordination polymer, [{Na(H2O)(H2btb)}{Cu4I(H2O)(pz)5Cl}{H2SrâP6Mo2VMo16VIO73}]·3H2O (1) (pz = pyrazine; btb = 1,4-bis(1,2,4-triazole) butane). Meanwhile, a zero-dimensional (0-D) control compound with only btb ligands as counterions, (H4btb)[H4SrâP6Mo2VMo16VIO73]·3H2O (2), was also obtained via a hydrothermal reaction. Compound 1 represents the first basket-type 3D poly(oxometalate) metal-organic framework (POMOF) assembly, which possesses interpenetrating pores and complex topology. 1-GO-CPE displays improved supercapacitor (SC) performance (the specific capacitance of 929.4 F g-1 at a current density of 3 A g-1 with 94.1% of cycle efficiency after 5000 cycles) compared with 2-GO-CPE and most reported POMOF electrode materials, which may be due to the outstanding redox capability of basket-POM, introduction of metal-organic chains, intersecting pores, and excellent conductivity of graphene. An asymmetric SC device with 1-GO-CPE as the negative electrode exhibits an energy density of 29.7 Wh kg-1 with a power density of 3148.2 W kg-1 and long-lasting cycling life. In addition, 1-GO-GCE as an electrochemical sensor responds to dopamine (DA) at a voltage of 0.40 V and shows lower detection limits (0.19 µM (signal-to-noise ratio (SNR) = 3)), higher selectivity, and good reproducibility in the linear range of 0.56 µM to 0.24 mM. The ability to accurately detect the content of DA in biological samples further proves the feasibility of the sensor in practical applications.
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Bulking agents are particularly important for sewage sludge composting. In this study, reusable polypropylene packing (RPP) was mixed with sawdust to improve composting. The effect of the mix ratio of sawdust and RPP on the physicochemical characteristics, nitrogen transformation, and emissions of greenhouse gas (GHG) as well as differences in the germination index values was detected in a lab-scale composting experiment. The results showed that the unique use of RPP as a bulking agent increased the moisture content over 70%, which resulted in poorer porosity and a less efficient O2 utilization environment and thus suppressed the degradation of organic matter. The highest CH4 9275.8 mg and lowest CO2 202.6 g emissions were detected after 25 days of composting in the treatment with RPP used as a bulking agent. When the mixing ratio of sawdust and RPP was 1:1, the temperature, oxygen supply, and dissolved organic carbon degradation were improved. The NH3, N2O, and CH4 emissions were reduced by 32.2, 18.3, and 90.7% compared with a treatment with RPP as a unique bulking agent. The RPP had no effect on conserving nitrogen during sludge composting; the total nitrogen loss was reduced from 29.3 to 18.2% when sawdust was mixed with RPP in a ratio of 1:1. Therefore, mixing RPP and sawdust in the dry weight ratio of 1:1 (sawdust: RPP) can be potentially used for reducing composting cost and improving the sewage sludge composting by reducing the amount of sawdust mixed and mitigating GHG and NH3 emissions.
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Compostagem , Gases de Efeito Estufa , Amônia/análise , Gases de Efeito Estufa/análise , Nitrogênio/análise , Polipropilenos , Esgotos , SoloRESUMO
The combination of persulfate (PDS) with micron-sized magnetite (Fe3O4) was introduced into the process of anaerobic fermentation (AF) to scrutinize the short chain fatty acid (SCFA) production from waste activated sludge for the first time. The synergetic effect of PDS and Fe3O4 results in the promotion of intracellular and extracellular substance liberation, augment in key hydrolases activities, and enrichment of hydrolytic and acidifying microbial population. Meanwhile, carbohydrate, amino acid, and energy metabolism as well as enzymes, are considerably accelerated. Consequently, the maximum SCFAs yield is significantly enhanced to 391.25 mg COD/L on day 8 of AF with the addition of 0.3 g Fe3O4/g SS and 0.5 g PDS/g SS, which was 2.39-folds than that of the control. The relative abundance of Actinobacteria were highly enriched and reached to 35.76% at the class level. This work affords an effective avenue to evidently boost the production of SCFAs from WAS via AF.
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Óxido Ferroso-Férrico , Esgotos , Anaerobiose , Ácidos Graxos Voláteis , Fermentação , Concentração de Íons de HidrogênioRESUMO
In this study, the effect of magnetite amendment on anaerobic digestion was investigated at three increasing salinity levels (0.5%, 1% and 2% NaCl). The amendment of magnetite enhanced the methane yield by 36.3%, 33.3% and 16.5% at low salinity (0.5% NaCl) and high salinity (1% and 2% NaCl), respectively. Meanwhile, a larger proportion of granules was obtained in the magnetite amended reactor (48.05% vs 33.16% at the end of operation). Microbial analysis suggested magnetite could induce more methanogenesis partnerships between hydrogenotrophic methanogens and syntrophic bacteria. Methanosaeta and Methanocorpusculum were the alternating dominant methanogens at low salinity and high salinity. While Streptococcus and Mesotoga were two prevalent bacteria that showed totally different transition tendency in two reactors. Additionally, the supplement of magnetite could relieve the suppression of methanogenesis-related gene expression caused by salinity, thus facilitated the higher methane production.