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Preparation and characterization of (10)B boric acid with high purity for nuclear industry

Boric acid is often added into coolant as neutron capture agent for pressurized water reactor, whose amount is influenced by its abundance and purity. Therefore, the preparation of enriched (10)B boric acid with high purity is beneficial to nuclear industry. (10)B is also used in developing tumor-sp...

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Autores principales: Zhang, Weijiang, Liu, Tianyu, Xu, Jiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963345/
https://www.ncbi.nlm.nih.gov/pubmed/27516940
http://dx.doi.org/10.1186/s40064-016-2310-6
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author Zhang, Weijiang
Liu, Tianyu
Xu, Jiao
author_facet Zhang, Weijiang
Liu, Tianyu
Xu, Jiao
author_sort Zhang, Weijiang
collection PubMed
description Boric acid is often added into coolant as neutron capture agent for pressurized water reactor, whose amount is influenced by its abundance and purity. Therefore, the preparation of enriched (10)B boric acid with high purity is beneficial to nuclear industry. (10)B is also used in developing tumor-specific boronated drugs in boron neutron capture therapy. The boronated drug can be administered to patient intravenously, intratumorally, or deposited at tumor site in surgical excision. Thus, enriched (10)B boric acid is of practical significance in the field of medicine. Self-made boron trifluoride–methanol-complex solution was selected as one of the experimental reagents, and the preparation of (10)B acid was realized by one-step reaction for the complexes with water and calcium chloride. The determination of electrical conductivity in reaction process proves that the optimum reaction time was 16–20 h. Furthermore, the effect of reaction time, ratio of calcium chloride to complex as well as the amount of water on the purity and yield of boric acid was investigated. Finally, the optimum reaction time was 20 h, the optimal solid–liquid ratio (molar ratio) was 3:1, and the amount of water was 1 L of deionized water for each mol of the complex. H(2)O(2) was added in the reaction process to remove Fe(2+). After recrystallization, IR spectra of (10)B boric acid was measured and compared with standard to verify the product of boric acid. The feasibility of the preparation method was determined by the detection of XRD of boric acid. To observe the morphology by polarizing microscope, crystal structure was obtained. The purity of the final product is 99.95 %, and the yield is 96.47 %. The ion concentration of boric acid accords with the national standard of high purity, which was determined by ICP.
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spelling pubmed-49633452016-08-11 Preparation and characterization of (10)B boric acid with high purity for nuclear industry Zhang, Weijiang Liu, Tianyu Xu, Jiao Springerplus Research Boric acid is often added into coolant as neutron capture agent for pressurized water reactor, whose amount is influenced by its abundance and purity. Therefore, the preparation of enriched (10)B boric acid with high purity is beneficial to nuclear industry. (10)B is also used in developing tumor-specific boronated drugs in boron neutron capture therapy. The boronated drug can be administered to patient intravenously, intratumorally, or deposited at tumor site in surgical excision. Thus, enriched (10)B boric acid is of practical significance in the field of medicine. Self-made boron trifluoride–methanol-complex solution was selected as one of the experimental reagents, and the preparation of (10)B acid was realized by one-step reaction for the complexes with water and calcium chloride. The determination of electrical conductivity in reaction process proves that the optimum reaction time was 16–20 h. Furthermore, the effect of reaction time, ratio of calcium chloride to complex as well as the amount of water on the purity and yield of boric acid was investigated. Finally, the optimum reaction time was 20 h, the optimal solid–liquid ratio (molar ratio) was 3:1, and the amount of water was 1 L of deionized water for each mol of the complex. H(2)O(2) was added in the reaction process to remove Fe(2+). After recrystallization, IR spectra of (10)B boric acid was measured and compared with standard to verify the product of boric acid. The feasibility of the preparation method was determined by the detection of XRD of boric acid. To observe the morphology by polarizing microscope, crystal structure was obtained. The purity of the final product is 99.95 %, and the yield is 96.47 %. The ion concentration of boric acid accords with the national standard of high purity, which was determined by ICP. Springer International Publishing 2016-07-28 /pmc/articles/PMC4963345/ /pubmed/27516940 http://dx.doi.org/10.1186/s40064-016-2310-6 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Zhang, Weijiang
Liu, Tianyu
Xu, Jiao
Preparation and characterization of (10)B boric acid with high purity for nuclear industry
title Preparation and characterization of (10)B boric acid with high purity for nuclear industry
title_full Preparation and characterization of (10)B boric acid with high purity for nuclear industry
title_fullStr Preparation and characterization of (10)B boric acid with high purity for nuclear industry
title_full_unstemmed Preparation and characterization of (10)B boric acid with high purity for nuclear industry
title_short Preparation and characterization of (10)B boric acid with high purity for nuclear industry
title_sort preparation and characterization of (10)b boric acid with high purity for nuclear industry
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963345/
https://www.ncbi.nlm.nih.gov/pubmed/27516940
http://dx.doi.org/10.1186/s40064-016-2310-6
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