Municipal solid waste incineration fly ash was selected as the alkaline Ca-bearing solid waste, and a series of direct aqueous carbonation experiments using 10% CO2 gas were conducted to showcase the capability of ultrafine bubbles (UFBs) in enhancing carbonation efficiency. Results from the experiments, conducted using a one-pass water flow system, revealed that carbonation without UFBs increased the CO2 content of the ash from 59 to 200 mgCO2/g (an increase of 141 mgCO2/g), while the presence of UFBs elevated it to 237 mgCO2/g (an increase of 178 mgCO2/g). Consequently, the introduction of UFBs led to a 26% increase in CO2 content in ash [(178−141) / 141]. This improvement was primarily attributed to the enhanced carbonation efficiency for particles ≥ 46 µm. The positive impact of UFBs was more evident (62% increase in CO2 content in ash) in experiments using a water circulation system, where carbonation proceeded at a faster rate compared to the one-pass water flow system. In terms of the mechanism, X-ray diffraction and scanning electron microscopy analyses indicated that UFBs facilitated the removal of CaCO3 deposition, which inhibited Ca(OH)2 dissolution. To the best of our knowledge, this study is the first to demonstrate the favorable influence of UFBs on fly ash carbonation efficiency.
{"title":"Application of ultrafine bubbles for enhanced carbonation of municipal solid waste incineration ash during direct aqueous carbonation","authors":"Tasuma Suzuki , Tatsushi Kawai , Yutaka Kamijima , Satoshi Shinohara , Mayumi Tanaka","doi":"10.1016/j.nxsust.2023.100020","DOIUrl":"https://doi.org/10.1016/j.nxsust.2023.100020","url":null,"abstract":"<div><p>Municipal solid waste incineration fly ash was selected as the alkaline Ca-bearing solid waste, and a series of direct aqueous carbonation experiments using 10% CO<sub>2</sub> gas were conducted to showcase the capability of ultrafine bubbles (UFBs) in enhancing carbonation efficiency. Results from the experiments, conducted using a one-pass water flow system, revealed that carbonation without UFBs increased the CO<sub>2</sub> content of the ash from 59 to 200 mgCO<sub>2</sub>/g (an increase of 141 mgCO<sub>2</sub>/g), while the presence of UFBs elevated it to 237 mgCO<sub>2</sub>/g (an increase of 178 mgCO<sub>2</sub>/g). Consequently, the introduction of UFBs led to a 26% increase in CO<sub>2</sub> content in ash [(178−141) / 141]. This improvement was primarily attributed to the enhanced carbonation efficiency for particles ≥ 46 µm. The positive impact of UFBs was more evident (62% increase in CO<sub>2</sub> content in ash) in experiments using a water circulation system, where carbonation proceeded at a faster rate compared to the one-pass water flow system. In terms of the mechanism, X-ray diffraction and scanning electron microscopy analyses indicated that UFBs facilitated the removal of CaCO<sub>3</sub> deposition, which inhibited Ca(OH)<sub>2</sub> dissolution. To the best of our knowledge, this study is the first to demonstrate the favorable influence of UFBs on fly ash carbonation efficiency.</p></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"3 ","pages":"Article 100020"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S294982362300020X/pdfft?md5=db6baf9aeced08ef8637e464daeb3b2d&pid=1-s2.0-S294982362300020X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139100973","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-01DOI: 10.1016/j.nxsust.2024.100037
Sailee S. Raut , Richa Singh , Utkarsha M. Lekhak
Nanotechnology represents a burgeoning scientific field that focuses on materials within the nanometer size range. Nanoparticles, categorized as incidental, engineered and naturally occurring nanoparticles (NONPs), constitute a critical aspect of nanotechnology. Incidental nanoparticles are inadvertently generated as byproducts, engineered nanoparticles are synthesized by humans for diverse applications and NONPs exist naturally in the environment. NONPs are further categorized based on their location in the environment, such as Naturally Occurring Carbon Nanoparticles, Naturally Occurring Metal Nanoparticles, NONPs present in food, NONPs of biological origin and NONPs present in the aquatic environment. NONPs exhibit ubiquity, spanning the atmosphere, hydrosphere, lithosphere and biosphere. They exhibit distinct properties in comparison to their bulk counterparts, such as a substantial surface area-to-volume ratio, immune-boosting capabilities, scavenger activity, nutritional significance and electron-donor attributes. NONPs have been utilized by humans since ancient times. Owing to these properties, they have been used unknowingly in various fields like medicine, cosmetics, decor, textile and the food industry. NONPs are found in artifacts such as Copper Ruby and the Lycurgus Cup, as well as in medicine, cosmetics and the food industry. Even today, NONPs continue to play pivotal roles in diverse fields such as cancer treatment, biosensors and the food industry. Also they contribute to environmental processes, soil fertility, nutrient transport and bioremediation. This review sheds light on multifaceted significance of NONPs in our evolving scientific landscape and comprehensively explores the history, sources, properties, types and uses of NONPs. It also focuses on the fate of NONPs in water, soil and plants and their environmental and human hazards. A special section on the environmental transformation of NONPs is included.
{"title":"Naturally occurring nanoparticles (NONPs): A review","authors":"Sailee S. Raut , Richa Singh , Utkarsha M. Lekhak","doi":"10.1016/j.nxsust.2024.100037","DOIUrl":"https://doi.org/10.1016/j.nxsust.2024.100037","url":null,"abstract":"<div><p>Nanotechnology represents a burgeoning scientific field that focuses on materials within the nanometer size range. Nanoparticles, categorized as incidental, engineered and naturally occurring nanoparticles (NONPs), constitute a critical aspect of nanotechnology. Incidental nanoparticles are inadvertently generated as byproducts, engineered nanoparticles are synthesized by humans for diverse applications and NONPs exist naturally in the environment. NONPs are further categorized based on their location in the environment, such as Naturally Occurring Carbon Nanoparticles, Naturally Occurring Metal Nanoparticles, NONPs present in food, NONPs of biological origin and NONPs present in the aquatic environment. NONPs exhibit ubiquity, spanning the atmosphere, hydrosphere, lithosphere and biosphere. They exhibit distinct properties in comparison to their bulk counterparts, such as a substantial surface area-to-volume ratio, immune-boosting capabilities, scavenger activity, nutritional significance and electron-donor attributes. NONPs have been utilized by humans since ancient times. Owing to these properties, they have been used unknowingly in various fields like medicine, cosmetics, decor, textile and the food industry. NONPs are found in artifacts such as Copper Ruby and the Lycurgus Cup, as well as in medicine, cosmetics and the food industry. Even today, NONPs continue to play pivotal roles in diverse fields such as cancer treatment, biosensors and the food industry. Also they contribute to environmental processes, soil fertility, nutrient transport and bioremediation. This review sheds light on multifaceted significance of NONPs in our evolving scientific landscape and comprehensively explores the history, sources, properties, types and uses of NONPs. It also focuses on the fate of NONPs in water, soil and plants and their environmental and human hazards. A special section on the environmental transformation of NONPs is included.</p></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"3 ","pages":"Article 100037"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S294982362400014X/pdfft?md5=ec4dd8aea12cb7caae6d29864355edcb&pid=1-s2.0-S294982362400014X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140554760","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-01DOI: 10.1016/j.nxsust.2024.100057
Na Qin , Chengxuan Tian , Laura Carter , Dan Tao , Yuxin Zhou , Fan Zhang
This study investigates an easy synthesis method of magnetic activated carbon (Fe3O4/AC) composites by ultrasonic mechanical blending of Fe3O4 particles and activated carbon (AC) powder at different mass ratios. The materials with the best performance were characterized by scanning electron microscope (SEM), energy dispersive spectroscopy (EDS), X-ray powder diffraction (XRD), specific surface and porosity analyzer (BET), hysteresis loop meter (VSM), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS). The as-prepared Fe3O4/AC was used to remove the contaminant methylene blue (MB) from solution. The effects of initial solution pH, material dosage, and temperature on MB removal were studied. A series of batch experiments demonstrated that the Fe3O4/AC with a mass ratio of Fe3O4 to AC = 1:5 showed a higher adsorption capacity of 251.3 ± 2.0 mg/g at 20 °C and pH = 6.5. Isotherm and kinetic studies indicated that the MB adsorption onto Fe3O4/AC was exothermic in a chemical monolayer adsorption process. The purification mechanism of Fe3O4/AC was investigated, FT-IR results showed that MB molecules adhered to Fe3O4/AC after purification. From the results of XPS full spectrum and high resolution spectrum, the possible purification mechanism is inferred as follows: electronic transfer between =N+ in MB and CO/C─O in Fe3O4/AC, as well as π-π interaction between the skeleton sheet of Fe3O4/AC and aromatic ring of MB. This study provides the theoretical reference and experimental basis for recovery and utilization of easily-obtained Fe3O4/AC to remove MB from wastewater.
{"title":"Economical magnetic activated carbon for methylene blue removal from water","authors":"Na Qin , Chengxuan Tian , Laura Carter , Dan Tao , Yuxin Zhou , Fan Zhang","doi":"10.1016/j.nxsust.2024.100057","DOIUrl":"https://doi.org/10.1016/j.nxsust.2024.100057","url":null,"abstract":"<div><p>This study investigates an easy synthesis method of magnetic activated carbon (Fe<sub>3</sub>O<sub>4</sub>/AC) composites by ultrasonic mechanical blending of Fe<sub>3</sub>O<sub>4</sub> particles and activated carbon (AC) powder at different mass ratios. The materials with the best performance were characterized by scanning electron microscope (SEM), energy dispersive spectroscopy (EDS), X-ray powder diffraction (XRD), specific surface and porosity analyzer (BET), hysteresis loop meter (VSM), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS). The as-prepared Fe<sub>3</sub>O<sub>4</sub>/AC was used to remove the contaminant methylene blue (MB) from solution. The effects of initial solution pH, material dosage, and temperature on MB removal were studied. A series of batch experiments demonstrated that the Fe<sub>3</sub>O<sub>4</sub>/AC with a mass ratio of Fe<sub>3</sub>O<sub>4</sub> to AC = 1:5 showed a higher adsorption capacity of 251.3 ± 2.0 mg/g at 20 °C and pH = 6.5. Isotherm and kinetic studies indicated that the MB adsorption onto Fe<sub>3</sub>O<sub>4</sub>/AC was exothermic in a chemical monolayer adsorption process. The purification mechanism of Fe<sub>3</sub>O<sub>4</sub>/AC was investigated, FT-IR results showed that MB molecules adhered to Fe<sub>3</sub>O<sub>4</sub>/AC after purification. From the results of XPS full spectrum and high resolution spectrum, the possible purification mechanism is inferred as follows: electronic transfer between =N<sup>+</sup> in MB and C<img>O/C─O in Fe<sub>3</sub>O<sub>4</sub>/AC, as well as π-π interaction between the skeleton sheet of Fe<sub>3</sub>O<sub>4</sub>/AC and aromatic ring of MB. This study provides the theoretical reference and experimental basis for recovery and utilization of easily-obtained Fe<sub>3</sub>O<sub>4</sub>/AC to remove MB from wastewater.</p></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"4 ","pages":"Article 100057"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949823624000345/pdfft?md5=7eb52195a1568e1ccdc7868a31484431&pid=1-s2.0-S2949823624000345-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141540215","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-01DOI: 10.1016/j.nxsust.2024.100061
Aranganathan Viswanathan, Vanchiappan Aravindan
Two reduced graphene oxides (rGO) were synthesized using two carbon sources, namely pristine graphite (rGO-PG), and recovered graphite (rGO-RG) (graphite recovered from spent Li-ion batteries) by modified hummers method and followed by the chemical reduction method to compare their supercapacitive performances. Their supercapacitance is found to be highly competitive and comparable with each other, except for their rate capabilities. The rate capability of rGO-RG is found to be inferior compared to rGO-PG. The supercapacitive behavior of both rGO’s was evaluated using five different aqueous electrolytes. The specific capacitance, specific energy, specific power, and columbic efficiencies exhibited by rGO-RG and rGO-PG were superior in the presence of 1 M H2SO4 and are 36 F g1, 7.1 Wh kg1, 0.88 kW kg1 and 96.55 %; and 40 F g1, 7.9 Wh kg1, 0.66 kW kg1 and 97.36 %, respectively. Both the rGOs exhibited no deterioration in their performance up to 10,000 continuous charge and discharge cycles at a current density of 10 A g1; rather, they exhibited enhancement in their performances with an increase in charge and discharge cycles. The enhancement exhibited by rGO-RG is superior to that of rGO-PG, which is 844 % (272 F g1) higher than its initial performance (29 F g1).
利用两种碳源,即原始石墨(rGO-PG)和回收石墨(rGO-RG)(从废旧锂离子电池中回收的石墨),采用改良嗡嗡法合成了两种还原石墨烯氧化物(rGO),然后采用化学还原法比较了它们的超级电容性能。结果发现,除了速率能力之外,它们的超级电容具有很强的竞争力,彼此不相上下。与 rGO-PG 相比,rGO-RG 的速率能力较差。使用五种不同的水性电解质对两种 rGO 的超级电容行为进行了评估。在 1 M H2SO4 的存在下,rGO-RG 和 rGO-PG 显示的比电容、比能量、比功率和电容效率都很高,分别为 36 F g1、7.1 Wh kg1、0.88 kW kg1 和 96.55 %;以及 40 F g1、7.9 Wh kg1、0.66 kW kg1 和 97.36 %。在电流密度为 10 A g1 的条件下,这两种 rGO 在连续充放电 10,000 次后性能没有下降;相反,随着充放电次数的增加,它们的性能有所提高。rGO-RG 的性能比 rGO-PG 高出 844 %(272 F g1),高于其初始性能(29 F g1)。
{"title":"The electrochemical comparisons of reduced graphene oxide synthesized from pristine and recovered graphite from spent Li-ion batteries","authors":"Aranganathan Viswanathan, Vanchiappan Aravindan","doi":"10.1016/j.nxsust.2024.100061","DOIUrl":"https://doi.org/10.1016/j.nxsust.2024.100061","url":null,"abstract":"<div><p>Two reduced graphene oxides (rGO) were synthesized using two carbon sources, namely pristine graphite (rGO-PG), and recovered graphite (rGO-RG) (graphite recovered from spent Li-ion batteries) by modified hummers method and followed by the chemical reduction method to compare their supercapacitive performances. Their supercapacitance is found to be highly competitive and comparable with each other, except for their rate capabilities. The rate capability of rGO-RG is found to be inferior compared to rGO-PG. The supercapacitive behavior of both rGO’s was evaluated using five different aqueous electrolytes. The specific capacitance, specific energy, specific power, and columbic efficiencies exhibited by rGO-RG and rGO-PG were superior in the presence of 1 M H<sub>2</sub>SO<sub>4</sub> and are 36 F g<sup><img>1</sup>, 7.1 Wh kg<sup><img>1</sup>, 0.88 kW kg<sup><img>1</sup> and 96.55 %; and 40 F g<sup><img>1</sup>, 7.9 Wh kg<sup><img>1</sup>, 0.66 kW kg<sup><img>1</sup> and 97.36 %, respectively. Both the rGOs exhibited no deterioration in their performance up to 10,000 continuous charge and discharge cycles at a current density of 10 A g<sup><img>1</sup>; rather, they exhibited enhancement in their performances with an increase in charge and discharge cycles. The enhancement exhibited by rGO-RG is superior to that of rGO-PG, which is 844 % (272 F g<sup><img>1</sup>) higher than its initial performance (29 F g<sup><img>1</sup>).</p></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"4 ","pages":"Article 100061"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949823624000382/pdfft?md5=3f7f049ec69839ddc5a7dfc09742eb76&pid=1-s2.0-S2949823624000382-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141595090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-01DOI: 10.1016/j.nxsust.2024.100054
Robert O. Gembo , Sebusi Odisitse , Titus A.M. Msagati , Cecil K. King’ondu
In this work, we report the use of spent rooibos tea leaves to fabricate activated carbon and use it to adsorptively remove the toxic Remazol Brilliant Blue R (RBBR) from the aqueous solution. The resulting activated carbon (SRTLAC) was characterized by Brunauer-Emmett-Teller N2 adsorption/desorption for surface area analysis, scanning electron microscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy, Raman spectroscopy, and X-ray diffraction for morphological, functional group and crystallinity analyses. A Taguchi design approach was employed to determine the optimal conditions for the RBBR adsorption onto SRTLAC. Among the process variables studied, the sorbent dosage, initial concentration, and pH predominantly affected the removal capacity. The maximum removal of 246.5 mg/g was attained at the highest initial RBBR concentration of 120 mg/L, solution pH of 2, sorbent dosage of 20 mg, and agitation time of 110 min. The analysis of variance results showed that RBBR initial concentration contributed the most significant percentage (95.33 %) towards the removal uptake, highlighting its considerable impact. The adsorption data collected at various concentrations (20 – 120 mg/L) were modelled using three non-linear regression isotherms and kinetic models. The Langmuir isotherm model provided the optimal fit for adsorption, suggesting a monolayer and homogenous sorption system with a maximum capacity of 491.38 mg/g. Meanwhile, the pseudo-2nd order kinetic models accurately elucidated the sorption mechanism. The RBBR species interacted with the SRTLAC functional groups via hydrogen bonding, dipole-dipole interactions, and ion-dipole forces. Therefore, SRTLAC presents a powerful tool for ridding the environment of RBBR dye pollution.
{"title":"Unlocking the valorization potential of Rooibos tea waste-derived activated carbon in the adsorptive removal of remazol brilliant blue R dye","authors":"Robert O. Gembo , Sebusi Odisitse , Titus A.M. Msagati , Cecil K. King’ondu","doi":"10.1016/j.nxsust.2024.100054","DOIUrl":"https://doi.org/10.1016/j.nxsust.2024.100054","url":null,"abstract":"<div><p>In this work, we report the use of spent rooibos tea leaves to fabricate activated carbon and use it to adsorptively remove the toxic Remazol Brilliant Blue R (RBBR) from the aqueous solution. The resulting activated carbon (SRTLAC) was characterized by Brunauer-Emmett-Teller N<sub>2</sub> adsorption/desorption for surface area analysis, scanning electron microscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy, Raman spectroscopy, and X-ray diffraction for morphological, functional group and crystallinity analyses. A Taguchi design approach was employed to determine the optimal conditions for the RBBR adsorption onto SRTLAC. Among the process variables studied, the sorbent dosage, initial concentration, and pH predominantly affected the removal capacity. The maximum removal of 246.5 mg/g was attained at the highest initial RBBR concentration of 120 mg/L, solution pH of 2, sorbent dosage of 20 mg, and agitation time of 110 min. The analysis of variance results showed that RBBR initial concentration contributed the most significant percentage (95.33 %) towards the removal uptake, highlighting its considerable impact. The adsorption data collected at various concentrations (20 – 120 mg/L) were modelled using three non-linear regression isotherms and kinetic models. The Langmuir isotherm model provided the optimal fit for adsorption, suggesting a monolayer and homogenous sorption system with a maximum capacity of 491.38 mg/g. Meanwhile, the pseudo-2<sup>nd</sup> order kinetic models accurately elucidated the sorption mechanism. The RBBR species interacted with the SRTLAC functional groups via hydrogen bonding, dipole-dipole interactions, and ion-dipole forces. Therefore, SRTLAC presents a powerful tool for ridding the environment of RBBR dye pollution.</p></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"4 ","pages":"Article 100054"},"PeriodicalIF":0.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S294982362400031X/pdfft?md5=bcbccf0e5aedb41111fdc3999aa23a3d&pid=1-s2.0-S294982362400031X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141482161","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-06-01DOI: 10.1016/j.nxsust.2023.100010
Falk Harnisch , Reinhold Lehneis
{"title":"The power grids need to be made ready for a circular and bio-based economy","authors":"Falk Harnisch , Reinhold Lehneis","doi":"10.1016/j.nxsust.2023.100010","DOIUrl":"10.1016/j.nxsust.2023.100010","url":null,"abstract":"","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"2 ","pages":"Article 100010"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949823623000107/pdfft?md5=f0ce246b593d157e45add8fc8f9bce00&pid=1-s2.0-S2949823623000107-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135614024","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-06-01DOI: 10.1016/j.nxsust.2023.100009
Dienifer F.L. Horsth , Julia de O. Primo , Jamille S. Correa , Fauze J. Anaissi , Xavier Noirfalise , Carla Bittencourt
Boehmite is a mineral of aluminum oxyhydroxide widely used as a catalyst support, adsorbent for dyes, and a key component in producing advanced optical and electronic devices. This study focuses on the synthesis of boehmite using recycled metallic aluminum through acid digestion (HCl) and subsequent precipitation by pH correction (NaOH). The aluminum source used was can seals, which were characterized using various techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). XRD analysis confirmed a boehmite-like phase of the recycled aluminum oxyhydroxide powder. SEM analysis revealed that the synthesized boehmite-like powder consisted of agglomerate plates, which influences its thermal and optical behavior, resulting in a lower dihydroxylation temperature and smaller band gap (∼3.7 eV) compared to the literature value (∼5.5 eV) for boehmite. The boehmite-like powder derived from recycling was used as a precursor for the synthesis of manganese aluminate (MnAl2O4). XRD analysis confirmed the formation of the MnAl2O4 galaxite phase, with XPS and absorbance spectroscopy in the visible region indicating the presence of mainly Mn2+ ions. The resulting brown manganese aluminate powder exhibited stability in harsh chemical environments, with a color change imperceptible to the human eye. Moreover, a near-infrared (NIR) reflectance of approximately 50% was achieved, superior to other brown pigments reported in the literature. These findings suggest that recycled aluminum can seals in aluminate have potential applications as pigments for coatings.
波姆石是一种氢氧化铝矿物,被广泛用作催化剂载体、染料吸附剂以及生产先进光学和电子设备的关键部件。本研究的重点是利用回收的金属铝,通过酸解(HCl)和随后的 pH 校正沉淀(NaOH)合成波姆石。使用的铝源是易拉罐封条,并使用各种技术对其进行了表征,包括 X 射线衍射 (XRD)、扫描电子显微镜 (SEM)、能量色散 X 射线光谱 (EDS) 和 X 射线光电子能谱 (XPS)。XRD 分析证实,回收的氢氧化铝粉末具有类似沸石的相。扫描电子显微镜分析表明,合成的沸石样粉末由团聚板组成,这影响了其热学和光学行为,导致其二羟化温度较低,带隙(∼3.7 eV)较沸石的文献值(∼5.5 eV)小。回收的沸石状粉末被用作合成锰铝酸盐(MnAl2O4)的前驱体。XRD 分析证实了 MnAl2O4 方铅矿相的形成,可见光区的 XPS 和吸光度光谱显示主要存在 Mn2+ 离子。生成的棕色铝酸锰粉末在恶劣的化学环境中表现出稳定性,其颜色变化肉眼难以察觉。此外,其近红外(NIR)反射率约为 50%,优于文献中报道的其他棕色颜料。这些研究结果表明,铝酸盐中的回收铝罐封条具有作为涂料颜料的潜在应用价值。
{"title":"Upcycling can seals into high-value boehmite-like for the synthesis of MnAl2O4: A circular economy approach","authors":"Dienifer F.L. Horsth , Julia de O. Primo , Jamille S. Correa , Fauze J. Anaissi , Xavier Noirfalise , Carla Bittencourt","doi":"10.1016/j.nxsust.2023.100009","DOIUrl":"10.1016/j.nxsust.2023.100009","url":null,"abstract":"<div><p>Boehmite is a mineral of aluminum oxyhydroxide widely used as a catalyst support, adsorbent for dyes, and a key component in producing advanced optical and electronic devices. This study focuses on the synthesis of boehmite using recycled metallic aluminum through acid digestion (HCl) and subsequent precipitation by pH correction (NaOH). The aluminum source used was can seals, which were characterized using various techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). XRD analysis confirmed a boehmite-like phase of the recycled aluminum oxyhydroxide powder. SEM analysis revealed that the synthesized boehmite-like powder consisted of agglomerate plates, which influences its thermal and optical behavior, resulting in a lower dihydroxylation temperature and smaller band gap (∼3.7 eV) compared to the literature value (∼5.5 eV) for boehmite. The boehmite-like powder derived from recycling was used as a precursor for the synthesis of manganese aluminate (MnAl<sub>2</sub>O<sub>4</sub>). XRD analysis confirmed the formation of the MnAl<sub>2</sub>O<sub>4</sub> galaxite phase, with XPS and absorbance spectroscopy in the visible region indicating the presence of mainly Mn<sup>2+</sup> ions. The resulting brown manganese aluminate powder exhibited stability in harsh chemical environments, with a color change imperceptible to the human eye. Moreover, a near-infrared (NIR) reflectance of approximately 50% was achieved, superior to other brown pigments reported in the literature. These findings suggest that recycled aluminum can seals in aluminate have potential applications as pigments for coatings.</p></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"2 ","pages":"Article 100009"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949823623000090/pdfft?md5=44b48860a28f4866b749b2c9052fa2c6&pid=1-s2.0-S2949823623000090-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136167073","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-06-01DOI: 10.1016/j.nxsust.2023.100013
David Sinkhonde
Nowadays the replacement of cement with pozzolanic materials is becoming a very hot topic as a result of CO2 emission challenges during cement production. Pore structures of pozzolanic materials allow understanding of their effects on pore parameters of cement-based composites. In this study, analytical solutions of surface porosity of waste brick powder (WBP) specimens generated from varying milling conditions were constructed using segmentation, watershed, and threshold algorithms. Scanning electron microscopy was combined with simulations of pore structures from Gwyddion leading to multi-scale driven surface porosity solutions. These methods for surface porosity characterisation of pozzolans can be boiled down to calls for sustainable construction. By implementing analytical methods, the porosity properties of WBP subjected to various milling conditions are successfully observed for the first time. Overall, the presented simulations using all the three methods proved that increasing the mass of clay bricks fed in ball mill reduced the fineness levels of WBP and increased the surface porosity values. It was shown that the porosity values from all the three methods ranged from 17% to 51%. The watershed simulations were noticed to underestimate the surface porosity values in comparison with threshold and segmentation simulations. The results on mean pore areas, number of pores, pore densities, pore volumes and mean pore sizes of WBP specimens were quite different from surface porosity results as variations became more evident for all three methods. The results from this research have highlighted that the proposed analytical solutions are fast and efficient in evaluating the overall behaviour of WBP in cement-based composites and represent reference points for engineering researchers involved in studies on supplementary cementitious materials.
{"title":"Analytical solutions of surface porosity of waste brick powder specimens from different milling conditions: A path towards sustainability","authors":"David Sinkhonde","doi":"10.1016/j.nxsust.2023.100013","DOIUrl":"https://doi.org/10.1016/j.nxsust.2023.100013","url":null,"abstract":"<div><p>Nowadays the replacement of cement with pozzolanic materials is becoming a very hot topic as a result of CO<sub>2</sub> emission challenges during cement production. Pore structures of pozzolanic materials allow understanding of their effects on pore parameters of cement-based composites. In this study, analytical solutions of surface porosity of waste brick powder (WBP) specimens generated from varying milling conditions were constructed using segmentation, watershed, and threshold algorithms. Scanning electron microscopy was combined with simulations of pore structures from Gwyddion leading to multi-scale driven surface porosity solutions. These methods for surface porosity characterisation of pozzolans can be boiled down to calls for sustainable construction. By implementing analytical methods, the porosity properties of WBP subjected to various milling conditions are successfully observed for the first time. Overall, the presented simulations using all the three methods proved that increasing the mass of clay bricks fed in ball mill reduced the fineness levels of WBP and increased the surface porosity values. It was shown that the porosity values from all the three methods ranged from 17% to 51%. The watershed simulations were noticed to underestimate the surface porosity values in comparison with threshold and segmentation simulations. The results on mean pore areas, number of pores, pore densities, pore volumes and mean pore sizes of WBP specimens were quite different from surface porosity results as variations became more evident for all three methods. The results from this research have highlighted that the proposed analytical solutions are fast and efficient in evaluating the overall behaviour of WBP in cement-based composites and represent reference points for engineering researchers involved in studies on supplementary cementitious materials.</p></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"2 ","pages":"Article 100013"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949823623000132/pdfft?md5=b8556367c655098905839d33d4174547&pid=1-s2.0-S2949823623000132-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138564376","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The increasing consumption of fossil fuels and petroleum products leads to high prices, depletion of natural resources, and increased global warming. Therefore, there is a critical need for an alternative, greener fuel that could replace fossil fuels. Biodiesel derived from plant-based oil or biomass is a renewable and non-toxic energy source and has emerged as an alternative to diesel. Today, biodiesel may be manufactured from a range of feedstock using a variety of catalysts and recovery processes thanks to advances in catalytic chemistry technology. Recently, metal oxide-based heterogeneous catalysts have been promising materials for the (trans)esterification reactions of oils to produce biodiesel. The review briefly describes the recent advances in heterogeneous catalysts based on metal oxides for biodiesel production. The pros and cons of various techniques and the mechanism of biodiesel synthesis by heterogeneous catalysts are discussed to understand the topic better. Lastly, the scope of future research and challenges are also presented.
{"title":"Metal oxide-based heterogeneous catalysts for biodiesel production","authors":"Vishal Gadore, Soumya Ranjan Mishra, Nidhi Yadav, Gaurav Yadav, Md. Ahmaruzzaman","doi":"10.1016/j.nxsust.2023.100012","DOIUrl":"https://doi.org/10.1016/j.nxsust.2023.100012","url":null,"abstract":"<div><p>The increasing consumption of fossil fuels and petroleum products leads to high prices, depletion of natural resources, and increased global warming. Therefore, there is a critical need for an alternative, greener fuel that could replace fossil fuels. Biodiesel derived from plant-based oil or biomass is a renewable and non-toxic energy source and has emerged as an alternative to diesel. Today, biodiesel may be manufactured from a range of feedstock using a variety of catalysts and recovery processes thanks to advances in catalytic chemistry technology. Recently, metal oxide-based heterogeneous catalysts have been promising materials for the (trans)esterification reactions of oils to produce biodiesel. The review briefly describes the recent advances in heterogeneous catalysts based on metal oxides for biodiesel production. The pros and cons of various techniques and the mechanism of biodiesel synthesis by heterogeneous catalysts are discussed to understand the topic better. Lastly, the scope of future research and challenges are also presented.</p></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"2 ","pages":"Article 100012"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949823623000120/pdfft?md5=87cd620a97186d3375ccdf06d8c35a6a&pid=1-s2.0-S2949823623000120-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138564375","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-06-01DOI: 10.1016/j.nxsust.2023.100005
Stéphane Mbiankeu Nguea
The working-age population is essential to the process of economic growth, and there is growing interest in understanding the demographic dividend's role in sustainable development, particularly in response to the challenge of environmental sustainability. The routes, however, via which the demographic dividend is likely to affect environmental sustainability, are poorly understood. This paper has provided a new case for a better understanding of the asymmetric effects of demographic dividend on environmental sustainability in African countries. To this end, we employed Driscoll-Kraay standard error and Instrumental Variable Generalized Method of Moments (IV-GMM) for a panel dataset of 32 African countries from 1996 to 2018. The empirical findings show that demographic dividend deteriorates environmental sustainability via an increase in the ecological footprint. The results also show that urbanization, globalization and renewable energy reduce ecological footprint. However, economic growth and ICT increase ecological footprint. Lastly, our findings highlight that economic growth, ICT, urbanization and FDI are channels through which demographic dividend affects environmental sustainability. Therefore, although supporting economic growth, Africa's working-age population also contributes to some degree to environmental pressure.
{"title":"Demographic dividend and environmental sustainability: The mediation effects of economic growth, ICT, foreign direct investment, and urbanization","authors":"Stéphane Mbiankeu Nguea","doi":"10.1016/j.nxsust.2023.100005","DOIUrl":"10.1016/j.nxsust.2023.100005","url":null,"abstract":"<div><p>The working-age population is essential to the process of economic growth, and there is growing interest in understanding the demographic dividend's role in sustainable development, particularly in response to the challenge of environmental sustainability. The routes, however, via which the demographic dividend is likely to affect environmental sustainability, are poorly understood. This paper has provided a new case for a better understanding of the asymmetric effects of demographic dividend on environmental sustainability in African countries. To this end, we employed Driscoll-Kraay standard error and Instrumental Variable Generalized Method of Moments (IV-GMM) for a panel dataset of 32 African countries from 1996 to 2018. The empirical findings show that demographic dividend deteriorates environmental sustainability via an increase in the ecological footprint. The results also show that urbanization, globalization and renewable energy reduce ecological footprint. However, economic growth and ICT increase ecological footprint. Lastly, our findings highlight that economic growth, ICT, urbanization and FDI are channels through which demographic dividend affects environmental sustainability. Therefore, although supporting economic growth, Africa's working-age population also contributes to some degree to environmental pressure.</p></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"2 ","pages":"Article 100005"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949823623000053/pdfft?md5=61dbaf659eacbb000503671ac89659eb&pid=1-s2.0-S2949823623000053-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135706272","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}