FA-SIFT study of the reactions of H₃O⁺∙(H₂O)n (n=0, 1, 2), NO⁺ and O₂˙⁺ with the terpenoid aldehydes citral, citronellal and myrtenal and their alcohol analogues

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Membrane electrolysis for separation of cobalt from terephthalic acid in industrial wastewater

Recovery of valuable metals from wastewaters containing both metals and organics is challenging with current technologies, in part due to their interactions. Typical approaches are chemical intensive. Here, we developed a membrane electrolysis system coupled to an acidic and alkaline crystallizer to enable separate precipitation of the organics and metals without additional chemicals. The target industrial wastewater contained mainly purified terephthalic acid (PTA), benzoic acid (BA), p-Toluic acid (PA), cobalt (Co), and manganese (Mn). We examined the removal and recovery efficiency of PTA and cobalt from two types of synthetic stream and the real process stream using several configurations. The acidic crystallizer reached a removal efficiency of PTA of 98.7 +/- 0.2% (Coulombic efficiency 99.71 +/- 0.2%, pH 3.03 +/- 0.18) in batch tests of the simple synthetic stream. The alkaline crystallizer achieved a cobalt recovery efficiency of 94.51 +/- 0.21% (Coulombic efficiency 87.67 +/- 0.31%, pH 11.37 +/- 0.21) in batch tests of the simple synthetic stream (TPA and Co). Then, the system was operated continuously with complex synthetic stream (TPA, BA, PA, Co and Mn). The alkaline crystallizer achieved a cobalt recovery efficiency of 97.78 +/- 0.02% (Coulombic efficiency 90.45 +/- 0.17%)at pH 11.68 +/- 0.02. The acidic crystallizer obtained a PTA removal efficiency of 61.2 +/- 0.1% (Coulombic efficiency 62.3 +/- 0.2%) over 144 h (pH 3.71 +/- 0.03). A real stream was tested over 5 h runs in batch showing 31.1 +/- 1.0% PTA (Coulombic efficiency 26.5 +/- 0.2%) and 82.92 +/- 0.22% cobalt removal (Coulombic efficiency 75.27 +/- 0.31%) at pH 2.71 +/- 0.12 and 8.07 +/- 0.02, respectively. However, micron-scale precipitates were generated from real stream tests. To conclude, the membrane electrolysis cell coupled with acidic and alkaline crystallizers enabled simultaneous separation of PTA and cobalt as solid precipitates from a complex stream with no chemical addition. The efficiencies were lower with the real stream than the synthetic streams, showing the impact of matrix effects and the need to optimize the performance of the crystallizers

The Magnitude of Global Marine Species Diversity

Background: The question of how many marine species exist is important because it provides a metric for how much we do and do not know about life in the oceans. We have compiled the first register of the marine species of the world and used this baseline to estimate how many more species, partitioned among all major eukaryotic groups, may be discovered. Results: There are ∼226,000 eukaryotic marine species described. More species were described in the past decade (∼20,000) than in any previous one. The number of authors describing new species has been increasing at a faster rate than the number of new species described in the past six decades. We report that there are ∼170,000 synonyms, that 58,000–72,000 species are collected but not yet described, and that 482,000–741,000 more species have yet to be sampled. Molecular methods may add tens of thousands of cryptic species. Thus, there may be 0.7–1.0 million marine species. Past rates of description of new species indicate there may be 0.5 ± 0.2 million marine species. On average 37% (median 31%) of species in over 100 recent field studies around the world might be new to science. Conclusions: Currently, between one-third and two-thirds of marine species may be undescribed, and previous estimates of there being well over one million marine species appear highly unlikely. More species than ever before are being described annually by an increasing number of authors. If the current trend continues, most species will be discovered this century

The Science Performance of JWST as Characterized in Commissioning

This paper characterizes the actual science performance of the James Webb Space Telescope (JWST), as determined from the six month commissioning period. We summarize the performance of the spacecraft, telescope, science instruments, and ground system, with an emphasis on differences from pre-launch expectations. Commissioning has made clear that JWST is fully capable of achieving the discoveries for which it was built. Moreover, almost across the board, the science performance of JWST is better than expected; in most cases, JWST will go deeper faster than expected. The telescope and instrument suite have demonstrated the sensitivity, stability, image quality, and spectral range that are necessary to transform our understanding of the cosmos through observations spanning from near-earth asteroids to the most distant galaxies.Comment: 5th version as accepted to PASP; 31 pages, 18 figures; https://iopscience.iop.org/article/10.1088/1538-3873/acb29

The James Webb Space Telescope Mission

Twenty-six years ago a small committee report, building on earlier studies, expounded a compelling and poetic vision for the future of astronomy, calling for an infrared-optimized space telescope with an aperture of at least $4m$. With the support of their governments in the US, Europe, and Canada, 20,000 people realized that vision as the $6.5m$ James Webb Space Telescope. A generation of astronomers will celebrate their accomplishments for the life of the mission, potentially as long as 20 years, and beyond. This report and the scientific discoveries that follow are extended thank-you notes to the 20,000 team members. The telescope is working perfectly, with much better image quality than expected. In this and accompanying papers, we give a brief history, describe the observatory, outline its objectives and current observing program, and discuss the inventions and people who made it possible. We cite detailed reports on the design and the measured performance on orbit.Comment: Accepted by PASP for the special issue on The James Webb Space Telescope Overview, 29 pages, 4 figure

Copper and zinc extraction from automobile shredder residues via an integrated electrodeposition and crystallization process

Automobile shredder residues (ASR) are produced during recycling processes from used cars and contain valuable metals such as copper and zinc. They constitute the fastest-growing industrial waste around the globe. Most of the produced ASR is thermally converted or ends up landfilled. With the increasing demand for valuable metals, the recovery of metals from ASR may serve as an alternative source for primary mining. Here we introduce an integrated metal recovery system combining leaching of metals from the target ASR waste using an ammonia lixiviant with electrodeposition, ammonia stripping, and crystallization to selectively recover copper and zinc as well as ammonia from ASR waste. The metals were first leached from the target ASR waste with an ammonia lixiviant. The obtained alkaline leachate (pH 9.6) was subsequently treated by electrodeposition, reaching a removal efficiency of 95.2 % for copper at a coulombic efficiency of 19.2 % and energy input of 12.4 kWh/kg Cu over 183 h. The further alkalization allowed for ammonia stripping, recovering 66.1 % of the ammonium as lixiviant at a temperature of 60°C. Final crystallization of zinc from the stripper effluent by continuous flushing of CO2 resulted in the recovery of 43.2 % as solid ZnCO3 at a neutral pH. Lixiviation was also performed using the treated effluent and recovered ammonia, and the same amount of copper was leached out from the residues showing full circularity of the lixiviant. This integrated system combining lixiviation, electrodeposition, ammonium stripping, and crystallization units is driven by electricity, with minimal input of chemicals and water

Exposure and health risk assessment from consumption of Pb contaminated water in Addis Ababa, Ethiopia

Exposure to lead (Pb) through drinking water has been linked to adverse health outcomes. Children are particularly susceptible. This study was designed to measure Pb contamination level in drinking water of the Ethiopian city Addis Ababa and assess the associated health risks. Eighty-eight fully-flushed drinking water samples were collected from all ten sub-cities of Addis Ababa. Pb concentration was measured using an Inductively Coupled Plasma Mass Spectrometer (ICP-MS). The chronic daily intake (CDI), the hazard quotient (HQ), and the cancer risk (CR) of Pb were determined to assess exposure levels and health effects. Blood lead level (B-Pb) for children was modelled using the integrated exposure uptake biokinetic model (IEUBK). The mean concentration of Pb in the drinking water was 17.8 mu g/l, where >50% of the samples exceeded WHO's 10 mu g/l guideline. Significant spatial variation of Pb was noticed among sub-cities. The mean CDI was 1.43 and 0.59 mu g/kg/day for children and adults, respectively. The HQ showed that 8% of children and 2.3% of adults exceeded the safe limit. The predicted geometric mean of B-Pb ranged from 3.23 to 14.65 mu g/dl. The risk of a child having a B-Pb level >5 mu g/dl at the median water Pb concentration (10.5 mu g/l) was estimated at 13.4%. Based on the 95th percentile Pb concentration (75.1 mu g/l), 89.6% of children would have B-Pb levels above the 5 mu g/dl threshold. The estimated CR was found in the range of 1 x 10(-7) to 9.9 x 10(-5); hence cancer risks are not a concern. The study concluded that Addis Ababa's drinking water is likely to be a source of lead exposure where consumers at specific city locations are at risk of numerous non-cancer health effects. The impacts are expected to be severe in the Ethiopian context; hence further investigations and coordinated interventions are require

Membrane electrolysis for separation of cobalt from terephthalic acid in industrial wastewater

Recovery of valuable metals from wastewaters containing both metals and organics is challenging with current technologies, in part due to their interactions. Typical approaches are chemical intensive. Here, we developed a membrane electrolysis system coupled to an acidic and alkaline crystallizer to enable separate precipitation of the organics and metals without additional chemicals. The target industrial wastewater contained mainly purified terephthalic acid (PTA), benzoic acid (BA), p-Toluic acid (PA), cobalt (Co), and manganese (Mn). We examined the removal and recovery efficiency of PTA and cobalt from two types of synthetic stream and the real process stream using several configurations. The acidic crystallizer reached a removal efficiency of PTA of 98.7 +/- 0.2% (Coulombic efficiency 99.71 +/- 0.2%, pH 3.03 +/- 0.18) in batch tests of the simple synthetic stream. The alkaline crystallizer achieved a cobalt recovery efficiency of 94.51 +/- 0.21% (Coulombic efficiency 87.67 +/- 0.31%, pH 11.37 +/- 0.21) in batch tests of the simple synthetic stream (TPA and Co). Then, the system was operated continuously with complex synthetic stream (TPA, BA, PA, Co and Mn). The alkaline crystallizer achieved a cobalt recovery efficiency of 97.78 +/- 0.02% (Coulombic efficiency 90.45 +/- 0.17%)at pH 11.68 +/- 0.02. The acidic crystallizer obtained a PTA removal efficiency of 61.2 +/- 0.1% (Coulombic efficiency 62.3 +/- 0.2%) over 144 h (pH 3.71 +/- 0.03). A real stream was tested over 5 h runs in batch showing 31.1 +/- 1.0% PTA (Coulombic efficiency 26.5 +/- 0.2%) and 82.92 +/- 0.22% cobalt removal (Coulombic efficiency 75.27 +/- 0.31%) at pH 2.71 +/- 0.12 and 8.07 +/- 0.02, respectively. However, micron-scale precipitates were generated from real stream tests. To conclude, the membrane electrolysis cell coupled with acidic and alkaline crystallizers enabled simultaneous separation of PTA and cobalt as solid precipitates from a complex stream with no chemical addition. The efficiencies were lower with the real stream than the synthetic streams, showing the impact of matrix effects and the need to optimize the performance of the crystallizers