scholarly journals How to Efficiently Produce Ultrapure Acids

2019 ◽  
Vol 2019 ◽  
pp. 1-5 ◽  
Author(s):  
Damiano Monticelli ◽  
Alessio Castelletti ◽  
Davide Civati ◽  
Sandro Recchia ◽  
Carlo Dossi

Subboiling distillation has been used since two decades for the purification of analytical grade acids from inorganic contaminants and demonstrated an efficient method to obtain pure acids starting from reagent grade chemicals. Nevertheless, the effect of the subboiling parameters on the purity of the distilled acids has never been methodically investigated. Aim of the present research is a systematic evaluation of the subboiling distillation protocol for the production of pure hydrochloric and nitric acid. In particular, the effect of the subboiling temperature and the number of subsequent distillations was investigated as these parameters were recognised as the most important factors controlling acid purity, acid concentration, and distillation yield. The concentration of twenty elements in the purified acids was determined by Inductively Coupled Plasma-Mass Spectrometry. As a result, the subboiling temperature (up to 82°C) and the number of subsequent distillations (up to four) were demonstrated not to affect the purity of the distilled nitric and hydrochloric acids. Under normal laboratory conditions, the residual elemental concentrations were in most cases below 10 ng/L in both nitric (2.75% w/w) and hydrochloric (0.1 M) blanks. Ultrapure nitric and hydrochloric acids could accordingly be produced under the most favorable conditions, i.e., the highest temperature and one distillation process only.

2008 ◽  
Vol 65 (6) ◽  
pp. 1153-1164 ◽  
Author(s):  
Carrol P. Hand ◽  
Stuart A. Ludsin ◽  
Brian J. Fryer ◽  
J. Ellen Marsden

Laurentian Great Lakes fishery management agencies are seeking ways to identify natal origins of parasitic- and spawning-phase sea lamprey ( Petromyzon marinus ) so that efforts to control this invasive species can be prioritized. We developed laser-ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) as a technique to quantify elemental concentrations in larval sea lamprey statoliths and explored the use of statolith microchemistry as a tool to discriminate among larval sea lamprey production streams. Our analyses demonstrate that (i) traversing across the statolith with the laser is preferable to drilling down through its apex, (ii) preserving specimens in 95% ethanol versus freezing them has minimal effects on elemental concentrations, (iii) a minimum of 15 individuals per stream should accurately depict stream-specific statolith elemental signatures, and (iv) LA-ICP-MS is preferable to particle-induced X-ray emission (PIXE) for statolith analysis, based on higher precision, lower cost, reduced sampling-time requirements, and wider availability. Using LA-ICP-MS, we could discriminate among larvae from 13 streams located in Lakes Michigan, Huron, and Superior with 82% classification accuracy, indicating that this tool holds promise for determining natal origins of sea lamprey in the Great Lakes.


2020 ◽  
Vol 58 (6) ◽  
pp. 873-882 ◽  
Author(s):  
Wencan Jiang ◽  
Gongwei Sun ◽  
Xinyu Wen ◽  
Shasha Men ◽  
Wenbin Cui ◽  
...  

AbstractIntroductionElement-tagged immunoassay coupled with inductively coupled plasma-mass spectrometry (ICP-MS) detection has the potential to revolutionize immunoassay analysis in clinical detection; however, a systematic evaluation with the standard guidelines of the assay is needed to ensure its performance meets the requirements of the clinical laboratory.MethodsCarcinoembryonic antigen (CEA) was chosen for analysis using the proposed method. A systematic evaluation of the proposed assay was carried out according to the Clinical and Laboratory Standards Institute (CLSI). The 469 clinical samples were analyzed using the new method and compared with the electrochemiluminescent immunoassay (ECLIA) method.ResultsThe measurement range of the assay was 1–900 ng/mL, with a detection limit of 0.83 ng/mL. The inter-assay and intra-assay imprecision were 4.67% and 5.38% with high concentration samples, and 9.27% and 17.64% with low concentration samples, respectively. The cross-reactivity (%) for different antigens was less than 0.05%, and the recovery was between 94% and 108%. Percentage deviation of all the dilutions was less than 12.5% during linearity estimation. The interference bias caused by different substances was less than 10%. The reference interval of the assay was 0–4.442 ng/mL. Comparison with the commercial ECLIA method for clinical sample detection, the proposed method showed a correlation of 0.9878 and no significant differences between the methods were observed (p = 0.6666).ConclusionsThe ICP-MS based immunoassay was successfully developed, and the analytical performance of the assay met the requirements of the CLSI, which fully proved the clinical transferability and application of the new method.


Author(s):  
Miguel Motas ◽  
Sandra Jiménez ◽  
José Oliva ◽  
Miguel Ángel Cámara ◽  
María Dolores Pérez-Cárceles

Human breast milk is the most complete foodstuff for infants but can also be a potential source of exposure to toxic chemicals. The aim of this study was to assess the levels of metal pollution in the breast milk of women living in agricultural and industrial/mining areas of the Region of Murcia (Spain) that are well known for their cases of environmental pollution. Human milk samples were collected from 50 mothers and inorganic contaminants were analyzed using inductively coupled plasma mass spectrometry (ICP-MS). The mean or maximum concentrations of the different inorganic elements analyzed in breast milk, with the exception of manganese, exceeded the maximum limits established by the WHO and could constitute a high risk for pregnant mothers and their children. The breast milk of women living in the industrial/mining zone presented the highest levels of aluminum, zinc, arsenic, lead, mercury and nickel. On the contrary, the highest concentrations of manganese, chromium and iron were determined in the milk of women living in the agricultural zone. These results suggested and confirmed different profiles of environmental contamination of these areas.


2018 ◽  
Vol 33 (10) ◽  
pp. 1784-1789 ◽  
Author(s):  
Lily Huang ◽  
Diane Beauchemin ◽  
Claude Dalpé

Elemental concentrations in melted solder can identify the type of solder used in a crime and narrow down suspects.


2020 ◽  
Author(s):  
Daniel Bůžek ◽  
Slavomír Adamec ◽  
Kamil Lang ◽  
Jan Demel

<div><p>UiO-66 is a zirconium-based metal-organic framework (MOF) that has numerous applications. Our group recently determined that UiO-66 is not as inert in aqueous dispersions as previously reported in the literature. The present work therefore assessed the behaviour of UiO-66 in buffers: 2-amino-2-(hydroxymethyl)-1,3-propanediol (TRIS), 4-(2-hydroxyethyl)piperazine-1-ethane sulfonic acid (HEPES), N-ethylmorpholine (NEM) and phosphate buffer (PB), all of which are commonly used in many UiO-66 applications. High pressure liquid chromatography and inductively coupled plasma mass spectrometry were used to monitor degradation of the MOF. In each buffer, the terephthalate linker was released to some extent, with a more pronounced leaching effect in the saline forms of these buffers. The HEPES buffer was found to be the most benign, whereas NEM and PB should be avoided at any concentration as they were shown to rapidly degrade the UiO-66 framework. Low concentration TRIS buffers are also recommended, although these offer minimal buffer capacity to adjust pH. Regardless of the buffer used, rapid terephthalate release was observed, indicating that the UiO-66 was attacked immediately after mixing with the buffer. In addition, the dissolution of zirconium, observed in some cases, intensified the UiO-66 decomposition process. These results demonstrate that sensitive analytical techniques have to be used to monitor the release of MOF components so as to quantify the stabilities of these materials in liquid environments.</p></div>


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