Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Protactinium
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
{{Use dmy dates|date=February 2021}} {{Infobox protactinium}} '''Protactinium''' is a [[chemical element]]; it has [[chemical symbol|symbol]] '''Pa''' and [[atomic number]] 91. It is a dense, [[radioactive]], silvery-gray [[actinide]] metal which readily reacts with [[oxygen]], water vapor, and inorganic [[acid]]s. It forms various [[chemical compound]]s, in which protactinium is usually present in the [[oxidation state]] +5, but it can also assume +4 and even +3 or +2 states. Concentrations of protactinium in the Earth's crust are typically a few parts per trillion, but may reach up to a few parts per million in some [[uraninite]] ore deposits. Because of its scarcity, high radioactivity, and high toxicity, there are currently no uses for protactinium outside scientific research, and for this purpose, protactinium is mostly extracted from [[spent nuclear fuel]]. The element was first identified in 1913 by [[Kazimierz Fajans]] and [[Oswald Helmuth Göhring]] and named "brevium" because of the short [[half-life]] of the specific [[isotope]] studied, [[Nuclear isomer|<sup>234m</sup>Pa]]. A more stable isotope of protactinium, <sup>231</sup>Pa, was discovered in 1917/18 by [[Lise Meitner]] in collaboration with [[Otto Hahn]], and they named the element protactinium.<ref name="meitner">{{cite journal | last=Meitner | first=Lise | title=Die Muttersubstanz des Actiniums, Ein Neues Radioaktives Element von Langer Lebensdauer | journal=Zeitschrift für Elektrochemie und angewandte physikalische Chemie | volume=24 | issue=11–12 | date=1918 | issn=0372-8323 | doi=10.1002/bbpc.19180241107 | pages=169–173}}</ref> In 1949, the [[IUPAC]] chose the name "protactinium" and confirmed Hahn and Meitner as its discoverers. The new name meant "(nuclear) [[precursor (chemistry)|precursor]] of [[actinium]],"<ref>{{cite web |title=Protactinium |url=http://hpschapters.org/northcarolina/NSDS/Protactinium.pdf |website=Human Health Fact Sheet |publisher=ANL (Argonne National Laboratory) |access-date=4 September 2023 |date=November 2001 |quote=The name comes from the Greek work protos (meaning first) and the element actinium, because protactinium is the precursor of actinium.}}</ref> suggesting that actinium is a product of radioactive decay of protactinium. [[John Arnold Cranston]] (working with [[Frederick Soddy]] and [[Ada Hitchins]]) is also credited with discovering the most stable isotope in 1915, but he delayed his announcement due to being called for service in the [[First World War]].<ref>[http://www.universitystory.gla.ac.uk/biography/?id=WH3023&type=P John Arnold Cranston] {{Webarchive|url=https://web.archive.org/web/20200311015550/http://www.universitystory.gla.ac.uk/biography/?id=WH3023&type=P |date=11 March 2020 }}. [[University of Glasgow]]</ref> The longest-lived and most abundant (nearly 100%) naturally occurring [[isotope]] of protactinium, <sup>231</sup>Pa, has a [[half-life]] of 32,760 years and is a decay product of [[uranium-235]]. Much smaller trace amounts of the short-lived <sup>234</sup>Pa and its [[nuclear isomer]] <sup>234m</sup>Pa occur in the decay chain of [[uranium-238]]. <sup>233</sup>Pa occurs as a result of the decay of [[thorium]]-233 as part of the chain of events necessary to produce [[uranium-233]] by neutron irradiation of <sup>232</sup>Th. It is an undesired intermediate product in [[Thorium-based nuclear power | thorium-based]] [[nuclear reactor]]s, and is therefore removed from the active zone of the reactor during the breeding process. Ocean science uses the element to understand the ancient ocean's geography: analysis of the relative concentrations of various uranium, thorium, and protactinium isotopes in water and minerals is used in [[radiometric dating]] of [[sediment]]s up to 175,000 years old, and in modeling of various geological processes.<ref>{{cite journal | last1 = Negre | first1 = César | display-authors = etal | year = 2010| title = Reversed flow of Atlantic deep water during the Last Glacial Maximum | url = https://www.pure.ed.ac.uk/ws/files/11751410/ReversedATlantic_Deep.pdf| journal = Nature | volume = 468 | issue = 7320| pages = 84–8 | doi = 10.1038/nature09508 | pmid = 21048764 | bibcode = 2010Natur.468...84N }}</ref>
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)