Close-in ice lines and the super-stellar C/O ratio in discs around very low-mass stars

The origin of the elevated C/O ratios in discs around late M dwarfs compared to discs around solar-type stars is not well understood. Here we endeavour to reproduce the observed differences in the disc C/O ratios as a function of stellar mass using a viscosity-driven disc evolution model and study the corresponding atmospheric composition of planets that grow inside the water-ice line in these discs. We carried out simulations using a coupled disc evolution and planet formation code that includes pebble drift and evaporation. We used a chemical partitioning model for the dust composition in the disc midplane. Inside the water-ice line, the disc's C/O ratio initially decreases to sub-stellar due to the inward drift and evaporation of water-ice-rich pebbles before increasing again to super-stellar values due to the inward diffusion of carbon-rich vapour. We show that this process is more efficient for very low-mass stars compared to solar-type stars due to the closer-in ice lines and shorter disc viscous timescales. In high-viscosity discs, the transition from sub-stellar to super-stellar takes place faster due to the fast inward advection of carbon-rich gas. Our results suggest that planets accreting their atmospheres early (when the disc C/O is still sub-stellar) will have low atmospheric C/O ratios, while planets that accrete their atmospheres late (when the disc C/O has become super-stellar) can obtain high C/O ratios. Our model predictions are consistent with observations, under the assumption that all stars have the same metallicity and chemical composition, and that the vertical mixing timescales in the inner disc are much shorter than the radial advection timescales. This further strengthens the case for considering stellar abundances alongside disc evolution in future studies that aim to link planet (atmospheric) composition to disc composition.Comment: Accepted for publication in A&

Phosphate removal from water using an iron oxide impregnated strong base anion exchange resin

Removing phosphate from water is important as it causes eutrophication, which in turn has a harmful effect on aquatic life, resulting in a reduction in biodiversity. On the other hand, recovery of phosphate from phosphorus containing wastewater is essential for developing an alternative source of phosphorus to overcome the global challenge of phosphorus scarcity. Phosphate removal from aqueous solutions was studied using an iron oxide impregnated strong base anion exchange resin, Purolite FerrIX A33E in batch and fixed-bed column experiments. Phosphate adsorption in the batch study satisfactorily fitted to the Langmuir isotherm with a maximum adsorption capacity of 48mgP/g. In the column study, increase in inlet phosphate concentration (5-30 mgP/L), and filtration velocity (2.5-10 m/h) resulted in faster breakthrough times and increase in breakthrough adsorption capacities. Increase in bed height (3-19 cm) also increased adsorption capacity but the breakthrough time was slower. The breakthrough data were reasonably well described using the empirical models of Bohart-Adams, Thomas, and Yoon-Nelson, except for high bed heights. Phosphate adsorbed was effectively desorbed using 1M NaOH and the adsorbent was regenerated after each of three adsorption/desorption cycles by maintaining the adsorption capacity at >90% of the original value. Greater than 99.5% of the desorbed P was recovered by precipitation using CaCl2. © 2013 The Korean Society of Industrial and Engineering Chemistry

Removing rubidium using potassium cobalt hexacyanoferrate in the membrane adsorption hybrid system

© 2017 Elsevier B.V. Highly-priced rubidium (Rb) can be effectively extracted from seawater using potassium cobalt hexacyanoferrate (KCoFC) and ammonium molybdophosphate (AMP) adsorbents in the membrane adsorption hybrid system (MAHS). KCoFC (<0.075 mm), KCoFC (0.075–0.15 mm), and AMP (<0.075 mm) had Langmuir adsorption capacities of 145, 113, and 77 mg/g at pH 6.5–7.5, respectively. When KCoFC (<0.075 mm) at a dose of 0.2 g/L was initially added to 4 L of a solution containing 5 mg Rb/L in the MAHS and 25% of the initial dose was repeatedly added every hour, the amount of Rb removed remained steady at 90–96% for the experiment's 26 h duration. The removal of Rb by AMP under similar conditions was 80–82%. The cumulative Rb removed by KCoFC (<0.075 mm) in MAHS was only 33% reduced in the presence of high concentrations of other cations in synthetic seawater compared to that in solution containing only Rb. Approximately 30% of the adsorbed Rb was desorbed using 1 M KCl. When the desorbed solution was passed through a column containing resorcinol formaldehyde (RF), 35% of the Rb in the desorbed solution was adsorbed on RF. Furthermore 50% of the Rb adsorbed on RF was recovered by 1 M HCl leaching of the column. This sequence of concentration and separation of Rb in the presence of other cations in synthetic seawater is an efficient method for recovering pure Rb from real seawater and seawater reverse osmosis brine

UASIS: Universal Automatic SNP Identification System

<p>Abstract</p> <p>Background</p> <p>SNP (Single Nucleotide Polymorphism), the most common genetic variations between human beings, is believed to be a promising way towards personalized medicine. As more and more research on SNPs are being conducted, non-standard nomenclatures may generate potential problems. The most serious issue is that researchers cannot perform cross referencing among different SNP databases. This will result in more resources and time required to track SNPs. It could be detrimental to the entire academic community.</p> <p>Results</p> <p>UASIS (Universal Automated SNP Identification System) is a web-based server for SNP nomenclature standardization and translation at DNA level. Three utilities are available. They are UASIS Aligner, Universal SNP Name Generator and SNP Name Mapper. UASIS maps SNPs from different databases, including dbSNP, GWAS, HapMap and JSNP etc., into an uniform view efficiently using a proposed universal nomenclature and state-of-art alignment algorithms. UASIS is freely available at <url>http://www.uasis.tk</url> with no requirement of log-in.</p> <p>Conclusions</p> <p>UASIS is a helpful platform for SNP cross referencing and tracking. By providing an informative, unique and unambiguous nomenclature, which utilizes unique position of a SNP, we aim to resolve the ambiguity of SNP nomenclatures currently practised. Our universal nomenclature is a good complement to mainstream SNP notations such as rs# and HGVS guidelines. UASIS acts as a bridge to connect heterogeneous representations of SNPs.</p

Polycrystalline Yttrium Aluminum Garnet Fibers from Colloidal Sols

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/66320/1/j.1151-2916.1995.tb08626.x.pd

Removing arsenic from water by coprecipitation with iron: Effect of arsenic and iron concentrations and adsorbent incorporation

© 2019 Elsevier Ltd Arsenic (As) contamination of drinking water is a major cause of As toxicity in many parts of the world. A study was conducted to evaluate As removal from water containing 100–700 μg/L of As and As to Fe concentration ratios of 1:5–1:1000 using the coprecipitation process with and without As/Fe adsorption onto granular activated carbon (GAC). Fe concentration required to reduce As concentrations in order to achieve the WHO standard level of 10 μg/L increased exponentially with the increase in initial As concentration. When small amounts of GAC were added to the As/Fe solutions the Fe required to remove these As concentrations reduced drastically. This decline was due to the GAC adsorption of Fe and As, enhancing the removal of these metals through coprecipitation. Predictive regression equations were developed relating the GAC dose requirement to the initial As and Fe concentrations. Zeta potential data revealed that As was adsorbed on the GAC by outer-sphere complexation whereas Fe was adsorbed by inner-sphere complexation reversing the negative charge on GAC to positive values. X-ray diffraction of the GAC samples in the presence of Fe had an additional peak characteristic of ferrihydrite (Fe oxide) compared to that of the GAC sample without Fe. The study showed that incorporating an adsorbent into the coprecipitation process has the advantage of removing As from waters at all concentrations of Fe and As compared to coprecipitation alone which does not remove As to the required levels if Fe concentration is low

Contribution of cod liver oil-related nutrients (vitamins A, D, E and eicosapentaenoic acid and docosahexaenoic acid) to daily nutrient intake and their associations with plasma concentrations in the EPIC-Norfolk cohort.

BACKGROUND: Total nutrient intake (TNI) is intake from food and supplements. This provides an assessment of nutrient adequacy and the prevalence of excessive intake, as well as the response with respect to biomarkers. Cod liver oil (CLO) is the most frequently consumed supplement in the UK, containing nutrients that might have varying influences on health. We calculated TNI for vitamins A, D and E, as well as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), and assessed associations with the respective blood concentrations. METHODS: Seven-day diet diaries and blood samples were taken from two subsets of the European Prospective Investigation into Cancer (EPIC-Norfolk) cohort (age range 39-79 years; n = 1400 for vitamin D; n = 6656 for remaining nutrients). TNI was calculated for the subgroups: nonsupplement users, those consuming the nutrient in supplement form and those consuming a supplement without this nutrient. RESULTS: CLO-related nutrients were supplemented by 15%-33%, which approximately doubled median intakes. Almost everyone in the supplement + vitamin A group reached the estimated average requirement; however, guideline levels were likely to be exceeded. Partial correlations between intake of vitamins A and D and biomarkers were low and modestly strengthened by the inclusion of supplement sources (correlation = 0.01-0.13). Correlations between biomarker and TNI of vitamin E and EPA+DHA were in the range 0.40-0.46; however, vitamin E exceeding food intake resulted in attenuated coefficients. Linear associations between food or TNI EPA+DHA and plasma were weak but consistent across subgroups. CONCLUSIONS: CLO-related nutrients contribute substantially to nutrient intake, with a risk of over-consumption. Apart from EPA+DHA, biomarker data suggest that CLO-related nutrients in supplements are not linearly associated with vitamin status.All authors report grants from Cancer Research UK and grants from the Medical Research Council (MRC) during the study.This is the final published manuscript, first published by Wiley in the Journal of Human Nutrition and Dietetics here: http://dx.doi.org/10.1111/jhn.1227

Carotenoid dietary intakes and plasma concentrations are associated with heel bone ultrasound attenuation and osteoporotic fracture risk in the European Prospective Investigation into Cancer and Nutrition (EPIC)-Norfolk cohort

Carotenoids are found in abundance in fruit and vegetables, and may be involved in the positive association of these foods with bone health. This study aimed to explore the associations of dietary carotenoid intakes and plasma concentrations with bone density status and osteoporotic fracture risk in a European population. Cross-sectional analyses (n 14 803) of bone density status, using calcaneal broadband ultrasound attenuation (BUA) and longitudinal analyses (n 25 439) of fracture cases were conducted on data from the prospective European Prospective Investigation into Cancer and Nutrition-Norfolk cohort of middle-aged and older men and women. Health and lifestyle questionnaires were completed, and dietary nutrient intakes were derived from 7-d food diaries. Multiple regression demonstrated significant positive trends in BUA for women across quintiles of dietary α-carotene intake (P=0·029), β-carotene intake (P=0·003), β-cryptoxanthin intake (P=0·031), combined lutein and zeaxanthin intake (P=0·010) and lycopene intake (P=0·005). No significant trends across plasma carotenoid concentration quintiles were apparent (n 4570). The Prentice-weighted Cox regression showed no trends in fracture risk across dietary carotenoid intake quintiles (mean follow-up time 12·5 years), except for a lower risk for wrist fracture in women with higher lutein and zeaxanthin intake (P=0·022); nevertheless, inter-quintile differences in fracture risk were found for both sexes. Analysis of plasma carotenoid data (mean follow-up time 11·9 years) showed lower hip fracture risk in men across higher plasma α-carotene (P=0·026) and β-carotene (P=0·027) quintiles. This study provides novel evidence that dietary carotenoid intake is relevant to bone health in men and women, demonstrating that associations with bone density status and fracture risk exist for dietary intake of specific carotenoids and their plasma concentrations.The EPIC-Norfolk study received grants from the Medical Research Council (G9502233) and from Cancer Research UK (SP2024-0201 and SP2024-0204)

Design of a pulse power supply unit for micro-ECM

Electrochemical micro-machining (μECM) requires a particular pulse power supply unit (PSU) to be developed in order to achieve desired machining performance. This paper summarises the development of a pulse PSU meeting the requirements of μECM. The pulse power supply provides tens of nanosecond pulse duration, positive and negative bias voltages and a polarity switching functionality. It fulfils the needs for tool preparation with reversed pulsed ECM on the machine. Moreover, the PSU is equipped with an ultrafast overcurrent protection which prevents the tool electrode from being damaged in case of short circuits. The developed pulse PSU was used to fabricate micro-tools out of 170 μm WC-Co alloy shafts via micro-electrochemical turning and drill deep holes via μECM in a disk made of 18NiCr6. The electrolyte used for both processes was a mixture of sulphuric acid and NaNO3 aqueous solutions.The research reported in this paper is supported by the European Commission within the project “Minimizing Defects in Micro-Manufacturing Applications (MIDEMMA)” (FP7-2011-NMP-ICT-FoF-285614