Amount Of Alkali Research Articles

Selective ion channel adsorbents facilitate efficient and low environmental impact extraction of liquid lithium resources

As lithium is the cornerstone of green energy development, it is crucial to realize a low environmental impact and efficient lithium extraction process. Ion-sieve adsorption is the most widely used method to extract liquid lithium resources, but this method is only efficient under alkaline conditions for H+ and Mg2+ competing adsorption. Conventional methods are often accompanied by the consumption of quantities of alkali, the generation of solid waste, and the acidification of liquid lithium resources. To address these issues, a selective ion-channel adsorbent was constructed. The composition comprises an ion sieve adsorbent and an organic carrier with a zwitterionic quaternary ammonium base group. This group storages OH-in situ, hinders H+ diffusion, slows down Mg2+ diffusion, and accelerates Li+ diffusion by relying on the difference in binding energies, which reduces the competing adsorption and avoids acidification and solid waste generation. The saturated adsorption capacity (21.38mg/g) and selectivity of the adsorbent are 4.7 and 24 times higher than that of conventional ion-sieve adsorbent under neutral conditions respectively. The dosage of alkali is 1/256 of the traditional method, the effluent remains neutral and no solid waste is generated. This study presents an environmental and effective adsorbent for lithium extraction.

Multiple element approach to P recovery and recycling: A green and sustainable strategy by using fused magnesia waste ash

Recovery of phosphorus through controlling the crystallization of struvite (MgNH4PO4·6H2O), a slow-release fertilizer, is highly attractive, but costly if large amounts of magnesium and alkali have to be added. In this study, a strategy for synchronously recovering phosphorus and nitrogen resources from wastewater and magnesium resources from solid waste was proposed. We demonstrated the fused magnesia waste ash (FMWA), an industrial by-product of magnesia which might serve as a cost-effective source of magnesium and alkali. The results showed that a recovery efficiency of 93.0 % PO43− and 88.8 % NH4+ from synthetic wastewater and 46.6 % Mg2+ from the FMWA was achieved when the ratio of [Mg2+]:[NH4+]:[PO43−] was 1.8:1:1. The magnesium release potential of FMWA was 10 times more than that of other known magnesium-containing solid wastes, due to the process in electric melting furnace damaged the lattice structure of magnesite and converted magnesite to magnesia. XRD analysis showed that crystalline struvite was the major product. The undissolved components of FMWA (MgCO3, MgO and SiO2) acted as crystal seeds, increasing the particle size and accelerating struvite precipitation. The application of FMWA for phosphorus fixation can reduce costs by 98.3 % compared with MgCl2. This research paves the way for employing FMWA in efficient recovery of phosphorus from wastewater, simultaneously achieving the resource utilization of industrial waste.

Realizing the single-crystalline LiNi0.90Mn0.05Co0.05O2 cathode with long-life and high-safety property driven by polysiloxane covering and PO43− doping

As a promising cathode for lithium-ion batteries, the ultra-high nickel content layered oxide LiNi0.90Co0.05Mn0.05O2 demonstrates the great attention for the high discharging capacity. However, the serious capacity attenuation resulted from the instable interface, crystal structure degeneration and strong side-reactions on cathode-electrolyte interphase with charging-discharging drastically restricts its extensive application. To alleviate the intrinsic drawbacks, the combination improvement strategy for polysiloxane covering and PO43− doping is adopted to lower the surface residual alkali amounts, defend the HF/F− attacking and enhance the cation location order of LiNi0.90Co0.05Mn0.05O2. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) are used to evaluate the synthesized samples. The cathodes after the polysiloxane covering and PO43− doping deliver the improved crystal structure, larger lattice parameters and superior electrochemical properties. The polysiloxane coated and PO43− doped sample exhibits a high discharging capacity of 147.5 mAh g−1 at 10.0C rate and 155.4 mAh g−1 at −30 °C, remains a capacity of 193.2 mAh g−1 at 1.0C after 300 cycles with a retention of 91.2 %. Besides, when applied in pouch full batteries, it could pass the rigorous safety tests of Bar impact, Overcharging test and Nail penetration successfully, and still maintain the superior cycling stability in practice application.

Selection of marine bacterial consortia efficient at degrading chitin leads to the discovery of new potential chitin degraders.

Chitin degradation is a keystone process in the oceans, mediated by marine microorganisms with the help of several enzymes, mostly chitinases. Sediment, seawater, and filter-feeding marine invertebrates, such as sponges, are known to harbor chitin-degrading bacteria and are presumably hotspots for chitin turnover. Here, we employed an artificial selection process involving enrichment cultures derived from microbial communities associated with the marine sponge Hymeniacidon perlevis, its surrounding seawater and sediment, to select bacterial consortia capable of degrading raw chitin. Throughout the artificial selection process, chitin degradation rates and the taxonomic composition of the four successive enrichment cultures were followed. To the best of our knowledge, chitin degradation was characterized for the first time using size exclusion chromatography, which revealed significant shifts in the numbered average chitin molecular weight, strongly suggesting the involvement of endo-chitinases in the breakdown of the chitin polymer during the enrichment process. Concomitantly with chitin degradation, the enrichment cultures exhibited a decrease in alpha diversity compared with the environmental samples. Notably, some of the dominant taxa in the enriched communities, such as Motilimonas, Arcobacter, and Halarcobacter, were previously unknown to be involved in chitin degradation. In particular, the analysis of published genomes of these genera suggests a pivotal role of Motilimonas in the hydrolytic cleavage of chitin. This study provides context to the microbiome of the marine sponge Hymeniacidon perlevis in light of its environmental surroundings and opens new ground to the future discovery and characterization of novel enzymes of marine origin involved in chitin degradation processes.IMPORTANCEChitin is the second most abundant biopolymer on Earth after cellulose, and the most abundant in the marine environment. At present, industrial processes for the conversion of seafood waste into chitin, chitosan, and chitooligosaccharide (COS) rely on the use of high amounts of concentrated acids or strong alkali at high temperature. Developing bio-based methods to transform available chitin into valuable compounds, such as chitosan and COS, holds promise in promoting a more sustainable, circular bioeconomy. By employing an artificial selection procedure based on chitin as a sole C and N source, we discovered microorganisms so-far unknown to metabolize chitin in the rare microbial biosphere of several marine biotopes. This finding represents a first important step on the path towards characterizing and exploiting potentially novel enzymes of marine origin with biotechnological interest, since products of chitin degradation may find applications across several sectors, such as agriculture, pharmacy, and waste management.

Calcium silicate hydrate complex konjac glucomannan-based hydrogel selectively adsorbed phosphate in low alkalinity solution

The selective recovery of phosphate from wastewater can manage nutrients and realize the recycling of phosphorus resources. In this study, a novel konjac glucomannan/pectin/calcium silicate composite hydrogel (KP-CSH) was developed for efficient recovery of phosphate in aqueous solution. The amount of alkali released after the reaction of KP-CSH in a neutral solution was small (the pH of the solution after the reaction was < 9). In a wide initial pH range (3–10), the adsorption capacity of KP-CSH in 50 mg-P/L phosphate solution reached 39∼45 mg-P/g. Besides, even if the pH of the solution after the reaction was less than 8, it could still well adsorb phosphate. The kinetic and isothermal adsorption experiments indicated that the adsorption process of phosphate by KP-CSH was chemical adsorption, and the maximum adsorption capacity was 61.2 mg-P/g. KP-CSH preferentially adsorbed phosphate even in the presence of high concentrations of competitive ions. In the actual biogas slurry, KP-CSH also exhibited the strongest selectivity/affinity for phosphate, and its distribution coefficient (Kd) was significantly higher than that of other co-existing anions and cations. The adsorption mechanism analysis indicated that Ca was the main adsorption site of KP-CSH, and that the adsorption process of target pollutants mainly involved ligand exchange and the intra-sphere complexation. Further plant seed germination and seedling growth experiments suggested that KP-CSH after phosphate recovery did not exert a negative effect on the growth of plant seedlings, and increased the chlorophyll content of seedling leaves. These results demonstrate that KP-CSH is a potential adsorbent for efficient phosphate recovery, which can be used as a slow-release phosphate fertilizer after recovering phosphate.

Utilization of papermaking black liquor as liquid phase for hydrothermal carbonization of corn stalks: The unique role of alkali for production of hydrochar

Papermaking black liquor (BL) contains a large amount of organic matter, alkali, and salt, which has high value in industrial and agricultural production. In the present paper, hydrothermal carbonization (HTC) technology has been employed to deal with BL and corn stalk (CS) under various conditions. A variety of analytical technologies, including Fourier Transform Infrared Spectrometer, X-Ray Diffraction, element analyzer, comprehensive thermal analyzer, scanning electron microscope, chromatography/mass spectrometry, TOC analyzer, and density functional theory (DFT), were used to characterize the physicochemical properties of hydrochar and aqueous phase product. The effects of experimental parameters (temperature, solid-liquid ratio, and time) on the HTC of BL and CS were systematically investigated. The higher energy yield and densification of hydrochar prepared by our HTC technology were obtained at 260 ℃ in 30 min with a solid-liquid ratio of 1:3. Mechanism study indicates that NaOH, which comes from the original BL, could effectively facilitate the cleavage of β–O–4 bond in lignin and β–1–4 glycosidic bond in cellulose and hemicellulose molecules. Hemicellulose and cellulose are more susceptible to degradation relevant to the lignin in the presence of NaOH. Elementary analysis shows that the dosage of BL is important for improving energy densification of hydrochar. The combustion characteristics show that hydrochar presents a thermochemical behavior, which is close to bituminous coal. Owing to hydroxyl ion in NaOH ion pair was consumed in the series of dehydrogenation reactions, pH of HTC aqueous phase product significantly decreases from 11 to 13 in original BL to 4.8–5. Such results indicate that a completely change for the components of BL could be obtained by our HTC technology, which provide a novel idea for the treatment of Papermaking BL without concentration.

Mercerisation Followed by Wet on Wet Reactive Dyeing of Cotton Fabric

The commonly employed textile wet processing methods are singeing, de-sizing, scouring, bleaching, mercerising, dying, printing, and finishing. However, these methods are more time-consuming and require a lot of energy, manpower, and chemicals. Therefore, this research aims to develop a semi-continuous processing route that minimizes these problems. In this study, two dying routes were employed. The first is a control group, which was done by conventional mercerisation and dyeing procedures, whereas the second is a semi-continuous experimental group, which has been employed by mercerisation followed by wet-on-wet (WOW) reactive dying. That is, after mercerisation, the fabric, which contains the optimum alkali concentration, goes to dyeing without washing. Washing and titration were performed to determine the optimum alkaline concentration in the fabric at a specific washing cycle. Fabrics that were washed at different cycles after mercerisation were dyed, and their washing fastness, degree of dye exhaustion, fixation, and colour strength were evaluated, and they had a slightly greater colour strength than conventionally dyed fabrics. This is because with a wet-on-wet dyeing procedure, the fabric is relaxed after mercerisation, which allows it to absorb more dye, and the leftover alkali in the fabric is used to fix the dye to the cellulose. The study shows that the optimal washing cycle for passing the optimum alkali concentration is one. Furthermore, the optimal amount of alkali remaining in the fabrics is 3–3.5%. As compared to the conventional dyeing process, this process is economical.

Administration of bicarbonates through percutaneous gastrostomy with continuous nocturnal infusion in a patient with Kearns-Sayre disease: a life changing therapeutical paradigm

BackgroundMitochondrial diseases (MDs) are systemic disorders that can affect multiple organs. Renal manifestations, including renal tubular acidosis, are common because kidneys are particularly vulnerable to energy deprivation. Treatment of MDs is often complex and electrolyte replacement can be difficult especially in pediatric patients, because large and repeated amounts of oral supplements are needed but are not well tolerated.Case presentationWe describe the case of a girl affected by Kearns-Sayre disease with severe renal tubular acidosis. The management of her metabolic acidosis was challenging because she showed persistent low levels of serum bicarbonates despite a progressive incrementation of oral bicarbonates. Furthermore, as a result to the ingestion of large amounts of alkali, the girl developed an aversion to oral supplementation. After positioning a percutaneous gastrostomy (PEG) and starting enteral administration of bicarbonates (with daily boluses and continuous nocturnal infusion), she finally obtained an adequate electrolyte control, with a significant increase in her quality of life.ConclusionsIn MDs, the combination of nocturnal continuous enteral administration of alkali plus diurnal boluses may represent a valid solution to correct metabolic acidosis. It can also result in an improved patients’ quality of life, particularly in pediatric settings, where compliance to oral therapy is often lacking due to the large and repeated amounts of unpalatable bicarbonates solutions required.

Substantially enhanced reaction of steel slag binder stimulated by the addition of sodium sulfate and thermal treatment

An industrial by-product of steel slag has a huge potential as an alternative binder and new supplementary cementitious material (SCM). In both pure steel slag and composite systems, the amount of sulfate can be a critical factor to control early-age performance. This study aims to improve the hydration of steel slag stimulated by using a small amount of Na2SO4. The results showed that 1 % Na2SO4 enhanced both C2(A,F) and C2S hydration, leading to improved strength and denser microstructures with the formation of ettringite, AFm, and siliceous hydrogarnet. Initial thermal treatment at 40 °C with 3 % Na2SO4 provided a fast development of compressive strength at 3 days over 15 MPa. Meanwhile, an excessive amount of alkali supplied by Na2SO4 affects the relative stability between SO4-rich AFm and ettringite and has a detrimental effect on mechanical performance. The result implies that Na2SO4 content should be precisely controlled when used as a stimulator in a composite system with steel slag.

Degradation of Sodium Acetate by Catalytic Ozonation Coupled with MnOx/NiOOH-Modified Fly Ash.

Fly ash, a type of solid waste generated in power plants, can be utilized as a catalyst carrier to enhance its value-added potential. Common methods often involve using a large amount of alkali for preprocessing, resulting in stable quartz and mullite forming silicate dissolution. This leads to an increased specific surface area and pore structure. In this study, we produced a catalyst composed of MnOx/NiOOH supported on fly ash by directly employing nickel hydroxide and potassium permanganate to generate metal active sites over the fly ash surface while simultaneously creating a larger specific surface area and pore structure. The ozone catalytic oxidation performance of this catalyst was evaluated using sodium acetate as the target organic matter. The experimental results demonstrated that an optimal removal efficiency of 57.5% for sodium acetate was achieved, surpassing even that of MnOx/NiOOH supported catalyst by using γ-Al2O3. After loading of MnOx/NiOOH, an oxygen vacancy is formed on the surface of fly ash, which plays an indirect oxidation effect on sodium acetate due to the transformation of ozone to •O2- and •OH over this oxygen vacancy. The reaction process parameters, including varying concentrations of ozone, sodium acetate, and catalyst dosage, as well as pH value and the quantitative analysis of formed free radicals, were examined in detail. This work demonstrated that fly ash could be used as a viable catalytic material for wastewater treatment and provided a new solution to the added value of fly ash.

Use of Alkaline-Activated Energy Waste Raw Materials in Geopolymer Concrete.

Silica fly ash, Certyd aggregate, and an alkaline solution were used to produce lightweight geopolymer concretes. The compressive strength, water absorption, and bulk density results, along with SEM photos showing the structure of the obtained composite, were obtained. Tests conducted on the specifications of lightweight geopolymer concretes have revealed significant chemical interactions between the ash aggregate and the geopolymer mortar, particularly when the coarse aggregate surface has been pre-treated with an alkaline solution. A statistical analysis of the experimental data, which investigated the influence of three key variables on the compressive strength, water absorption, and bulk density of lightweight geopolymer concrete (LBG), identified the following factors as having the most substantial impact: the quantity of alkali used, the curing temperature, and the concentration of alkali in the mixture. The optimal test series exhibited a commendable compressive strength of 20.14 megapascals (MPa), accompanied by a water absorption rate of 14.72%, and a bulk density of 1486.6 kg per cubic meter (kg/m³). These findings underscore the importance of alkali content, curing temperature, and alkali concentration in tailoring the properties of lightweight geopolymer concrete to meet specific performance requirements.

Groundwater Quality and Suitability Assessment in Tirupur Region, Tamil Nadu, India

The study aims to understand the hydrochemical characteristics and groundwater suitability for agricultural and drinking purposes. For this purpose, 21 groundwater samples were collected, and major physicochemical parameters such as pH, EC, TDS, temp, salinity, Ca2+, Mg2+, Na+, K+, HCO3−, Cl−, and SO42− were analyzed, followed by the standard analytical procedures. Different groundwater quality graphical representations were constructed by using Aqua Chem software. The results indicate groundwater samples were alkaline with fresh to moderate saline in nature, sixty-eight percent of the samples were suitable for drinking in accordance with WHO, and thirty-two percent of the samples were unsuitable due to the excess amount of different ionic concentrations derived from natural and various anthropogenic sources. Irrigation water quality parameters such as SAR, EC, PI, Na %, RSBC, MR, and KR were used to understand the irrigation suitability. The US salinity diagram exemplifies that most groundwater samples fall in the C3S1 category with high salinity hazard and low alkali hazard. The Wilcox plot reveals that 80% of the samples were found under very good to permissible limits, and few samples fall with doubtful to unsuitable quality due to the excess amount of alkali and salinity. Permeability index values show that groundwater is suitable for irrigation. Three major hydrochemical facies were identified with the dominance order of mixed CaMgCl, NaCl, and CaCl. Gibb’s plot suggests that evaporation and rock-water interaction are the dominant natural mechanisms controlling the groundwater chemistry in the present study area.

Recovery of alkali in Gracilaria agar production by electrodialysis and membrane concentration

Industrial Gracilaria agar extraction consumes a large amount of alkali. The previous strategy was to directly reuse the alkali to extract agar. It eventually led to the accumulation of chemical oxygen demand (COD) in the alkali solution, resulting in the failure of alkali functions. The large amount of COD and alkali from alkali-treated Gracilaria results in resource waste and environmental damage. For this reason, electrodialysis and membrane concentration were used to recover the low-concentration alkali in alkali-treated Gracilaria, and the physicochemical properties of Gracilaria agar extracted by recovered alkali from different methods were evaluated. Results shown that the COD removal rate and the alkali recovery rate of the recovered alkaline solution by electrodialysis reached 69.97 % and 45.31 %, respectively. Furthermore, the optimal conditions for low-concentration alkali membrane concentration were pressure of 0.50 MPa, flow rate of 40 L/h, and pore size of 1000 Da. Under these conditions, the highest COD removal rate and the alkali recovery rate of recovered alkaline solution by membrane concentration reached 68.46 % and 11.20 %, respectively. The gel strength of agar extracted by electrodialysis and from a low-alkaline solution after five times of membrane concentration increased by 18.2 % and 15.7 %, respectively, compared with those extracted by the traditional method. The X-ray fluorescence spectra indicated that elemental K and Ca from the recovered alkali could improve the gel strength of agar. Electron microscopy analysis and Fourier transform infrared spectroscopy revealed no significant differences in the gel skeleton and functional group structure between the recovered alkali-extracted agar and traditional method-extracted agar. After electrodialysis and membrane concentration, the cumulative alkali recovery rate of alkali-treated Gracilaria could reach 37.14 %. This study provided new ideas for the clean production of agar and other marine polysaccharides.

Industrial-scale highly efficient nickel recovery from electroplating wastewater using resin adsorption followed by aeration mixing acid regeneration

Cation-exchange resins have been used to recover nickel from electroplating wastewater, but resin regeneration often consumes a large amount of acid and alkali, resulting in low Ni(II) concentrations in regenerating solution. In this study, the industrial-scale Ni(II) recovery from electroplating wastewater using resin adsorption and regeneration was investigated. Two cation-exchange resin tanks and one chelated resin tank in series effectively reduced the nickel concentrations to below 0.1 mg/L. The spent resin could be efficiently regenerated by a novel aeration mixing method, greatly reducing acid and alkali consumption in comparison with the traditional downstream regeneration method. The spent resin was successfully regenerated by 2 bed volume (BV) of 6 % HCl, and the acid utilization ratio was above 99 %. More than 60 g/L of Ni(II) ions in regenerating solution was stably obtained, which benefited the subsequent nickel recovery by electrodeposition. Similarly, H2SO4 was also effective for Ni(II) desorption from the spent resins. The adsorption and regeneration cost was calculated to be ¥ 5.5–9.5/m3 for the electroplating wastewater containing 200–800 mg/L Ni(II) ions, much lower than that by chemical precipitation. This study provided an effective resin regeneration method to consume less regenerants and obtain higher Ni(II) concentrations, making the Ni(II) recovery cost-effective.

Deep-UV Raman spectroscopy: A novel heuristic method to characterize volcanologically relevant glasses on Mars

Deep ultraviolet Raman spectroscopy is an essential component of the Perseverance rover operating on Mars. Here we propose a proof of concept of deep-UV Raman structural characterization of volcanologically relevant silicate glasses to provide a suitable analytical method of UV Raman spectra collected on Mars. The results show few but substantial spectral differences concerning those obtained by conventional Raman scattering using visible light laser sources. The evolution of the UV Raman spectra between 825 and 1300 cm−1 is confirmed to be more sensitive to the silica network's short-range structure than that below 700 cm−1 when compared to their visible counterpart. We adopted a Gaussian fitting model to parametrize the number of bridging oxygens resulting from the tetrahedral‑oxygens stretching vibrations along a sub-alkaline join of volcanic glasses. We used these parameters to empirically provide a relation with the glass silica content. The model was externally validated with glasses having different and known compositions (in particular different amounts of iron, alkali and alumina) extending the validation set also to other magmatic series (i.e. alkaline and shoshonitic). Our approach enables a fast screening of deep-UV Raman spectra collected on Mars to disentangle the glass structure and retrieve its silica content within a given magmatic series. This method is relevant for planetary exploration and applies both to microanalysis of dry or hydrate volcanologically relevant glasses and general technical glasses since deep-UV Raman spectroscopy is particularly effective in reducing the unwished photoluminescence and increasing the signal-to-noise ratio.

Influence of the availability of calcium hydroxide, sulphates, and alkalis on hydration of supplementary cementitious materials

The hydration of siliceous fly ash (FA), slag (S) and metakaolin (MK) with calcium hydroxide (CH) was studied at 27 °C to isolate the roles of CH, alkali and sulphate. The influence on rate of hydration was studied along with phase assemblage and strength development. While the FA was the most slowly reacting SCM, it was also the least influenced by the addition of alkalis and sulphates. For MK and S, not only the rate of hydration is influenced, but the phases formed are also affected by the amount of alkalis and sulphates. The addition of sulphates delays the hydration of alumina in S and MK. In more reactive SCMs such as MK, the availability of CH can be a limiting factor in the reaction of the SCM. The results show that to achieve maximum possible hydration and contribution to strength by SCMs, an optimisation of the alkali and sulphate content is required.

Research on the ratio of multicomponent emulsion flooding system

In recent years, field test and industrialized application of ASP (alkaline/surfactant/polymer) flooding has been carried out in oilfields, which has obtained an obvious effect on increasing oil and decreasing water and good economic efficiency. However, due to the large proportion of alkali in the ASP flooding system, there are problems such as severe scaling and high cost during field tests, which restrict the promotion of ASP flooding. In order to reduce the amount of alkali used, achieve the goal of reducing scaling and costs, and meanwhile improve emulsification performance while maintaining interfacial activity, a multicomponent emulsion flooding system was developed by combining emulsifier HEFR2 with petroleum sulfonate and sacrificial agent LSCP1 with NaOH.Through laboratory experiments, the water extraction rate, particle diameter, Tsi value, and interfacial activity of the multicomponent emulsion flooding system were tested under different conditions. The results show that when the mass ratio of petroleum sulfonate to emulsifier HEFR2 is between 3:1 and 5:1, and the mass ratio of sacrificial agent LSCP1 to NaOH is between 3:1 and 7:1, the multicomponent emulsion flooding system can maintain good emulsification stability and interfacial activity. The multicomponent emulsion flooding system significantly reduces the amount of alkali used, and the cost of chemical agents is 11% lower than that of the ASP flooding system. At the same time, it achieves the goal of improving the stability of emulsifiers, maintains interfacial activity and reduces costs. This technology has broad application prospects.

The purification of acid mine drainage through the formation of schwertmannite with Fe(0) reduction and alkali-regulated biomineralization prior to lime neutralization

Acid mine drainage (AMD) contains abundant Fe (II), Fe(III), and SO42−, as well as a large amount of dissolved toxic metals and metalloids, posing a serious threat to the environment. In this study, an integrated technique for the treatment of AMD was proposed. The technique started with pre-oxidation followed by Fe(0) reduction and alkali-regulated biomineralization and then ended with lime neutralization. The technique removed toxic metal oxyanions in the pre-oxidation stage and recovered pure schwertmannite during the subsequent alkali-regulated biomineralization. Fe(III), which could not be directly biomineralized, was reduced to Fe(II) by Fe(0). A small amount of alkali was added to regulate the hydrolytic mineralization reaction after Fe(II) oxidation in AMD, which in a single biomineralization could remove in the form of schwertmannite >95 % of soluble Fe in the AMD. In the subsequent lime neutralization process, the amount of lime required and the sludge produced were reduced by 75.4 % and 84.9 %, respectively, compared to the raw AMD. Additionally, the content of non-ferrous metals in the sludge increased 5.6-fold. Compared with non-alkali-regulated biomineralization, the schwertmannite obtained by the alkali-regulated biomineralization had a higher adsorption capacity for oxyanions (e.g., arsenic, chromium, and antimony). The new approach should significantly reduce the treatment cost of AMD and recover Fe and S elements in the form of valuable secondary minerals, such that it is reasonable to expect that it will be widely adopted in practical applications.

The Highly Enhanced Efficiency of the Photocatalytic Reduction of CO2 over Bi2WO6 Nanosheets by NaOH Microregulation

The photoreduction of CO2 to other products containing carbon through simulated photosynthesis is a promising area of research. However, given the complexity of the CO2 photocatalytic reduction reaction, it is crucial to adjust the structure of the photocatalysts. The focus of this study was on creating NaOH-modified Bi2WO6 nanosheet photocatalysts via a one-step hydrothermal route and using them to convert CO2 into CO through photocatalytic reduction under the condition of not using an electron sacrifice agent. The results of characterizations and activity data showed that adding an appropriate amount of NaOH significantly improved the photoreduction activity of CO2, as seen in the BWO-2 catalyst. The efficiency of photocatalysts could be improved by tuning the band structure through the addition of an appropriate amount of alkali. This adjustment improves the separation of photogenerated carriers and controls the concentration of oxygen vacancy to reduce recombination. As a result, the photocurrent activity is highly enhanced, leading to better reduction performance compared to unmodified photocatalysts. In experiments, the CO yield of the modified photocatalyst BWO-2 remained above 90 μmol/g after four trials, indicating its effectiveness in reducing CO2. This study offers insights into the regulation of band structure in bismuth-based photocatalysts for efficient CO2 reduction.

New attempts on acidic anaerobic digestion of poly (butylene adipate-co-terephthalate) wastewater in upflow anaerobic sludge blanket reactor

Poly (butylene adipate-co-terephthalate) (PBAT) wastewater is a highly concentrated, acidic, and toxic wastewater generated from biodegradable plastics production. Large amounts of alkali would be consumed when treating PBAT wastewater by anaerobic digestion due to the low pH value. This study employed acidic anaerobic digestion to treat PBAT wastewater and compared to neutral anaerobic digestion. The results indicated that the COD removal rates in the acidic upflow anaerobic sludge blanket (UASB) reactor were 65.5% and 59.9%, respectively at influent pH 6.0 and 5.0 with the COD concentration of around 11,000 mg L−1, and the methane conversion efficiency were 172.5 and 183.8 mLCH4/gCODr (gCODr: COD removed amount), respectively. Correspondingly, the average COD removal and methane conversion efficiency in the neutral UASB reactor were 63.2% and 188.0 mLCH4/gCODr, respectively. The treatment efficiency of acidic and neutral UASB reactors for PBAT wastewater was similar. The hydrogenotrophic methanogenic activity was further enhanced in the acidic UASB reactor compared to the neutral one. The increase of alkalinity in the acidic UASB reactor (2.4 mmol L−1) was higher than the neutral (2.0 mmol L−1). A higher level of syntrophic acetate oxidation bacteria and hydrogenotrophic methanogen was enriched in the acidic UASB reactor, ensuring efficient treatment and saving costs.