ラベル Radionuclide の投稿を表示しています。 すべての投稿を表示
ラベル Radionuclide の投稿を表示しています。 すべての投稿を表示

2017年3月30日木曜日

水素爆発(福島)

水素爆発(福島)

水素爆発
  1. 気体の水素(水素分子)によるガス爆発。水素#水素分子およびガス爆発を参照。
  2. 水素原子の核融合反応によるエネルギー放出の急激なもの。水素爆弾における反応。原子核融合を参照。
チェルノブイリ原子力発電所事故や福島第一原子力発電所事故など、核分裂反応を利用する原子力発電所の事故(冷却機能の喪失)により起きる爆発は上記1である[1]。燃料被覆管のジルカロイが高温の水蒸気と反応して水素が発生し、次いで水素が酸素と反応して爆発する。
Zr + 2 H2O → ZrO2 + 2 H2
2 H2 + O2 → 2 H2O
原子力事故におけるこのような爆発はしばしば2の核爆発と混同されるが、全く別の現象である[2][3]。

脚注

  1. ^ Nuclear Fuel Behaviour in Loss-of-coolant Accident (LOCA) Conditions. Nuclear Energy Agency, OECD. (2009). ISBN 978-92-64-99091-3. PDF
  2. ^ 今中哲二「水素爆発か核爆発か?--チェルノブイリ原発4号炉爆発の正体」、『技術と人間』第31巻第6号、2002年、 78-91頁、 NAID 40005419420。 今中はチェルノブイリ原発事故で起きた爆発を即発臨界で大量のエネルギーが放出されたことによる爆発であると解釈し、その現象を「一種の『核爆発』」と表現したが、それも核兵器による核爆発とは異なるものである。
  3. ^ 福島第一原子力発電所の事故についての Q and A - 北海道大学大学院 工学研究院

関連項目

2017年3月26日日曜日

Fukushima Revitalization

Fukushima Prefecture > Fukushima Revitalization Station

Radioactivity measurement map

(※) Radiation Map of the Pref.

3月25日 土曜日 17時 Now
Map image of the background
Fukushima City
0.17μSv/h
Kooriyama City
0.10μSv/h
Shirakawa City
0.07μSv/h
Aizuwakamatsu City
0.05μSv/h
Minamiaizu Town
0.04μSv/h
Minamisoma City
0.08μSv/h
Iwaki City
0.07μSv/h
Tokyo Shinjuku
0.03μSv/h
(※) As main points of 7 departments in Fukushima Prefecture, we post doses of radioactivity at each Government building. Shinjuku-ku, Tokyo is reference level. As for the details including dose of radioactivity of other points, please click 'detailed info' which leads to Fukushima Prefecture Radioactivity Measurement Map.
[related information] about "influence of radiation in everyday life"
Japanese major cities (unit μSv/h)
The city name (atomic energy regulation agency data)
Sapporo city 0.03 March 22, 2017
Tokyo 0.03 March 22, 2017
Fukuoka city 0.06 March 22, 2017
Overseas major cities (unit μSv/h)
The city name (data source:Japan National Tourism Organization)
New York 0.04 Mar12, 2017
London 0.10 Mar13, 2017
Singapore 0.10 Mar13, 2017
Hong Kong 0.09-0.15 Mar13, 2017
Beijing 0.07 Mar13, 2017

2017年3月11日土曜日

取水口付近に8.7 m〜9.2 mの津波が襲来するものの陸上への遡上は無いとした報告

東京電力は、2006年9月に日本の原子力安全委員会の耐震設計審査指針[189]が改定されたことを受けて、2002年7月の地震調査委員会の三陸沖から房総沖にかけての日本海溝付近ではどこでもマグニチュード8クラスの地震が起きる可能性があるとの評価結果を踏まえ[190]、福島県沖での地震発生を想定し津波の高さは10 mを超えると結論付け、2008年に津波の想定を従来の試算5.7 mから10 m以上に引き上げていたということを2011年8月事故調査・検証委員会の委員長畑村洋太郎に明らかにしている[191]。この試算では明治三陸地震と同規模の地震が起こると仮定し、海水取水口付近で津波の高さは8.4 m〜10.2 m、遡上高は1〜4号機で15.7 m、5号機・6号機で13.7 mとした[192]。また、この試算後産業技術総合研究所は貞観地震の津波被害も評価し、取水口付近に8.7 m〜9.2 mの津波が襲来するものの陸上への遡上は無いとした報告を2009年9月に原子力安全・保安院へ行っている[192]。

2015年5月30日土曜日

今度はシナ海に

放射能汚染海域の拡大、地表汚染被害、環境破壊民族が自らの地を汚染させる愚かな行為、捏造しようが、虚偽であろうが環境破壊の事実に変わりはない。違いがあるとするなら利権で誰が得をしたのか?である。被害者は住民であり、貧乏くじをひかされるのは世界共通の事実である。九州地方と言えば、長崎原爆の被災地、第三候補の原爆投下実験の候補、運が悪いとしか、事故としか言いようがない。 日本が仕掛けた戦争、略奪テロリストの大日本帝国、帝国崩壊を賭けた大東亜戦争、東洋の野蛮人の異名は、未だ健在、衰えてはいない。日本人の根底にある自己破滅型の精神、この精神構造が世界に類を見ない異色の文化を築いたのでしょう。日本の怪奇現象の一つ、騙されやすい国民性が国を滅ぼすのである。支那海域の汚染はこれから始まる川内原発爆破事故?事故ではなく行為的には爆破実験であり、地表汚染拡大のための原子炉強度、噴火耐震性の問題のための確信犯である。騙される住民が叫び狂う恐怖の大地に一番適した原子力発電所が薩摩川内原発、南蛮渡来の文化を伝える薩摩の国、歴史的な因果関係が見え隠れする原子力問題、幕末の遺恨であるかのように会津藩から薩摩藩えと被災地が移動した。
 意図的な環境破壊、日本の原子炉崩壊の裏舞台、意図的に仕組まれていると思うのは考え過ぎであろうか?政府は被爆保障で自爆を考えているのでは?核心なのかもしれません。

2015年4月21日火曜日

ポンプ停止、汚染雨水が再び海洋流出 福島第1原発

東京電力は21日、福島第1原発の「K排水路」と呼ばれる排水路から、別の排水路へ移送するためのポンプ8台が全て停止し、汚染雨水が外洋(港湾外)へ流出したと発表した。発電機の故障でポンプが停止したためで、予備の発電機を稼働させて移送を再開する予定。K排水路は2月にも、流出データを9カ月間公表しなかったことが問題となった場所で、漁業関係者らの反発が強まっている。  東電によると、巡回中の作業員が21日午前8時45分ごろ、外洋につながるK排水路から、港湾内につながる排水路(C排水路)に汚染雨水を移送するポンプが停止し、海側にある堰(せき)を越えて外洋に流出しているのを見つけた。ポンプは最大で1時間当たり約1700トンを移送できるといい、20日午後の時点では正常に稼働していたという。  汚染雨水が流出したK排水路では9日時点で、ストロンチウム90などのベータ線を出す放射性物質の濃度が1リットル当たり22ベクレル(法定基準30ベクレル)だった。今回流出した量や濃度は不明。 また、2月に外洋流出が表面化した後も、ポンプによる移送開始までの1カ月半以上、第1原発構内に降った雨水などの汚染水流出が続いていたことも明らかになった。  福島県はこの日、県庁に東電の担当者を呼び、早急の原因究明と再発防止策を講じるよう申し入れた。同県の相馬双葉漁業協同組合の関係者は「とにかく汚染水を海に出さないように、対策を万全にしてほしい」と憤っていた。(原子力取材班)

2015年3月18日水曜日

Nuclear Power Plant, Bushehr

Nuclear Power Plant, Bushehr

From Wikipedia, the free encyclopedia
Nuclear Power Plant, Bushehr
نيروگاه اتمي
village/company town
Country Iran
ProvinceBushehr
CountyBushehr
BakhshCentral
Rural DistrictHowmeh
Population (2006)
 • Total3,341
Time zoneIRST (UTC+3:30)
 • Summer (DST)IRDT (UTC+4:30)
Nuclear Power Plant, Bushehr (Persian: نيروگاه اتمي‎ – Nīrūgāh Ātomī) is a village and company town in Howmeh Rural District, in the Central District of Bushehr County, Bushehr Province, Iran. At the 2006 census, its population was 3,341, in 921 families.[1]

References[edit]

2015年3月13日金曜日

汚染水外洋流出9カ月“隠蔽”した東電「原因判明してから公表しようと」の危機的情報公開意識

東京電力福島第1原発の汚染水問題が再び“炎上”した。汚染水が排水路を通じて外洋(港湾外)に流出しているにもかかわらず、9カ月近く公表しなかった東電の体質に批判が集中。ろくに対応策を講じなかった国への不信も増幅している。東電は急場しのぎで外洋への流出防止策を打ち出したが、抜本的な解決とは言い難い。いつになったら安心できるのか、漁業者や周辺住民の怒りは収まらない。(原子力取材班) ひたすら謝る東電幹部  「今回は、避難されている住民や国民の皆様方に不信感をさらにもたれる状況になり、データの扱いや公表の仕方で、われわれに落ち度があったと考えている。今回は大変なご迷惑をかけて申し訳ありませんでした」  東電の原子力部門のトップ、姉川尚史常務は3月4日、原子力規制委員会の福島第1原発監視検討会で、ひたすら頭を下げ続けた。  汚染水の流出経路となったのは、1~4号機の原子炉建屋の西側を通る「K排水路」と呼ばれる水の通り道で、地下に埋まっている。2号機の建屋屋上には、事故時の放射性物質が降り積もっており、雨が降るたびに汚染された雨水が排水路を通じて外洋に流れ出していたとするデータを東電は2月末に公表した。

2014年3月28日金曜日

Radionuclide

Radionuclide

From Wikipedia, the free encyclopedia
A radionuclide, or a radioactive nuclide, is an atom with an unstable nucleus, characterized by excess energy available to be imparted either to a newly created radiation particle within the nucleus or via internal conversion. During this process, the radionuclide is said to undergo radioactive decay, resulting in the emission of gamma ray(s) and/or subatomic particles such as alpha or beta particles.[1] These emissions constitute ionizing radiation. Radionuclides occur naturally, or can be produced artificially.
Radionuclides are often referred to by chemists and physicists as radioactive isotopes or radioisotopes. Radioisotopes with suitable half-lives play an important part in a number of technologies (for example, nuclear medicine). Radionuclides can also present both real and perceived dangers to health.
The number of radionuclides is uncertain because the number of very short-lived radionuclides that have yet to be characterized is extremely large and potentially unquantifiable. Even the number of long-lived radionuclides is uncertain (to a lesser degree), because many "stable" nuclides are calculated to have half-lives so long that their decay has not been experimentally measured. The total list of nuclides contains 90 nuclides that are, in theory, stable, and 254 total stable nuclides that have not been observed to decay. In addition, however, there exist 34 primordial radionuclides that exist from the creation of the solar system, plus another 50 radionuclides detectable in nature as daughters of these, plus a few produced by cosmic radiation. Including artificial radionuclides, about 650 radionuclides that have been experimentally observed to decay, with half-lives longer than 60 minutes (see list of nuclides for this list). Of all these, less than a hundred natural radionuclides are known (they have been observed on Earth, but not as a consequence of human activity).
Including artificially produced nuclides, more than 3300 nuclides are known (including ~3000 radionuclides), many of which (> ~2400) with decay half-lives shorter than 60 minutes. This list expands as new radionuclides with very short half-lives are characterized.
All elements form a number of radionuclides, although the half-lives of many are too short for them to be observed in nature. Even the lightest element, hydrogen, has a well-known radioisotope, tritium. The heaviest elements (heavier than bismuth) exist only as radionuclides. For every chemical element, many radioisotopes that do not occur in nature (due to short half lives or the lack of an ongoing natural production mechanism), have been produced artificially.

Origin

Naturally occurring radionuclides fall into three categories: primordial radionuclides, secondary radionuclides, and cosmogenic radionuclides. Primordial radionuclides, such as uranium and thorium, originate mainly from the interiors of stars and are still present as their half-lives are so long they have not yet completely decayed. Secondary radionuclides are radiogenic isotopes derived from the decay of primordial radionuclides. They have shorter half-lives than primordial radionuclides. Cosmogenic isotopes, such as carbon-14, are present because they are continually being formed in the atmosphere due to cosmic rays.[2]
Artificially produced radionuclides can be produced by nuclear reactors, particle accelerators or by radionuclide generators:
  • Radioisotopes produced with nuclear reactors exploit the high flux of neutrons present. These neutrons activate elements placed within the reactor. A typical product from a nuclear reactor is thallium-201 and iridium-192. The elements that have a large propensity to take up the neutrons in the reactor are said to have a high neutron cross-section.
  • Particle accelerators such as cyclotrons accelerate particles to bombard a target to produce radionuclides. Cyclotrons accelerate protons at a target to produce positron-emitting radionuclides, e.g., fluorine-18.
  • Radionuclide generators contain a parent radionuclide that decays to produce a radioactive daughter. The parent is usually produced in a nuclear reactor. A typical example is the technetium-99m generator used in nuclear medicine. The parent produced in the reactor is molybdenum-99.
  • Radionuclides are produced as an unavoidable side-effect of nuclear and thermonuclear explosions.
Trace radionuclides are those that occur in tiny amounts in nature either due to inherent rarity or due to half-lives that are significantly shorter than the age of the Earth. Synthetic isotopes are inherently not naturally occurring on Earth, but can be created by nuclear reactions.

Uses

Radionuclides are used in two major ways: for their chemical properties and as sources of radiation. Radionuclides of familiar elements such as carbon can serve as radioactive tracers because they are chemically very similar to the nonradioactive nuclides, so most chemical, biological, and ecological processes treat them in a nearly identical way. One can then examine the result with a radiation detector, such as a Geiger counter, to determine where the provided atoms ended up. For example, one might culture plants in an environment in which the carbon dioxide contained radioactive carbon; then the parts of the plant that had laid down atmospheric carbon would be radioactive.
In nuclear medicine, radioisotopes are used for diagnosis, treatment, and research. Radioactive chemical tracers emitting gamma rays or positrons can provide diagnostic information about a person's internal anatomy and the functioning of specific organs. This is used in some forms of tomography: single-photon emission computed tomography and positron emission tomography scanning and Cerenkov luminescence imaging.
Radioisotopes are also a method of treatment in hemopoietic forms of tumors; the success for treatment of solid tumors has been limited. More powerful gamma sources sterilise syringes and other medical equipment.
In biochemistry and genetics, radionuclides label molecules and allow tracing chemical and physiological processes occurring in living organisms, such as DNA replication or amino acid transport.
In food preservation, radiation is used to stop the sprouting of root crops after harvesting, to kill parasites and pests, and to control the ripening of stored fruit and vegetables.
In industry, and in mining, radionuclides examine welds, to detect leaks, to study the rate of wear, erosion and corrosion of metals, and for on-stream analysis of a wide range of minerals and fuels.
Radionuclides are also used to trace and analyze pollutants, to study the movement of surface water, and to measure water runoffs from rain and snow, as well as the flow rates of streams and rivers. Natural radionuclides are used in geology, archaeology, and paleontology to measure ages of rocks, minerals, and fossil materials.

Common examples

Americium-241

Americium-241 container in a smoke detector.
Americium-241 capsule as found in smoke detector. The circle of darker metal in the center is americium-241, the surrounding casing is aluminium.
Most household smoke detectors contain americium produced in nuclear reactors. The radioisotope used is americium-241. The element americium is created by bombarding plutonium with neutrons in a nuclear reactor. Its isotope, Am-241 decays by emitting alpha particles and gamma radiation to become neptunium-237. Most common household smoke detectors use a very small quantity of Am-241 (about 0.29 micrograms per smoke detector) in the form of americium dioxide. Smoke detectors use Am-241 since the alpha particles it emits collide with oxygen and nitrogen particles in the air. This occurs in the detector's ionization chamber where it produces charged particles or ions. Then, these charged particles are collected by a small electric voltage that will create an electric current that will pass between two electrodes. Then, the ions that are flowing between the electrodes will be neutralized when coming in contact with smoke, thereby decreasing the electric current between the electrodes, which will activate the detector's alarm.[3][4]

Steps for creating americium-241

The plutonium-241 is formed in any nuclear reactor by neutron capture from uranium-238.
  1. 238U + n → 239U
  2. 239U → 239Np + e− + ν
    e
  3. 239Np → 239Pu + e− + ν
    e
  4. 239Pu + n → 240Pu
  5. 240Pu + n → 241Pu
This will decay both in the reactor and subsequently to form Am-241, which has a half-life of 432.2 years.[5][6]

Gadolinium-153

The Gd-153 isotope is used in X-ray fluorescence and osteoporosis screening. It is a gamma-emitter with an 8-month half-life, making it easier to use for medical purposes. In nuclear medicine, it serves to calibrate the equipment needed like single-photon emission computed tomography systems (SPECT) to make x-rays. It ensures that the machines work correctly to produce images of radioisotope distribution inside the patient. This isotope is produced in a nuclear reactor from europium or enriched gadolinium.[7] It can also detect the loss of calcium in the hip and back bones, allowing the ability to diagnose osteoporosis.[8]

Dangers

Radionuclides that find their way into the environment may cause harmful effects as radioactive contamination. They can also cause damage if they are excessively used during treatment or in other ways exposed to living beings, by radiation poisoning. Potential health damage from exposure to radionuclides depends on a number of factors, and "can damage the functions of healthy tissue/organs. Radiation exposure can produce effects ranging from skin redness and hair loss, to radiation burns and acute radiation syndrome. Prolonged exposure can lead to cells being damaged and in turn lead to cancer. Signs of cancerous cells might not show up until years, or even decades, after exposure."[9]

Summary table for classes of nuclides, "stable" and radioactive

Following is a summary table for the total list of nuclides with half-lives greater than one hour. Ninety of these 905 nuclides are theoretically stable, except to proton-decay (which has never been observed). About 254 nuclides have never been observed to decay, and are classically considered stable.
The remaining 650 radionuclides have half-lives longer than 1 hour, and are well-characterized (see list of nuclides for a complete tabulation). They include 28 nuclides with measured half-lives longer than the estimated age of the universe (13.8 billion years[10]), and another 6 nuclides with half-lives long enough (> 80 million years) that they are radioactive primordial nuclides, and may be detected on Earth, having survived from their presence in interstellar dust since before the formation of the solar system, about 4.6 billion years ago. Another ~51 short-lived nuclides can be detected naturally as daughters of longer-lived nuclides or cosmic-ray products. The remaining known nuclides are known solely from artificial nuclear transmutation.
Numbers are not exact, and may change slightly in the future, as "stable nuclides" are observed to be radioactive with very long half-lives.
This is a summary table [11] for the 905 nuclides with half-lives longer than one hour (including those that are stable), given in list of nuclides.
Stability class Number of nuclides Running total Notes on running total
Theoretically stable to all but proton decay 90 90 Includes first 40 elements. Proton decay yet to be observed.
Energetically unstable to one or more known decay modes, but no decay yet seen. Spontaneous fission possible for "stable" nuclides > niobium-93; other mechanisms possible for heavier nuclides. All considered "stable" until decay detected. 164 254 Total of classically stable nuclides.
Radioactive primordial nuclides. 34 288 Total primordial elements include uranium, thorium, bismuth, rubidium-87, potassium-40 plus all stable nuclides.
Radioactive nonprimordial, but naturally occurring on Earth. ~ 51 ~ 339 Carbon-14 (and other isotopes generated by cosmic rays) and daughters of radioactive primordial elements, such as radium, polonium, etc.
Radioactive synthetic (half-life > 1.0 hour). Includes most useful radiotracers. 556 905 These 905 nuclides are listed in the article List of nuclides.
Radioactive synthetic (half-life < 1.0 hour). >2400 >3300 Includes all well-characterized synthetic nuclides.

List of commercially available radionuclides

This list covers common isotopes, most of which are available in very small quantities to the general public in most countries. Others that are not publicly accessible are traded commercially in industrial, medical, and scientific fields and are subject to government regulation. For a complete list of all known isotopes for every element (minus activity data), see list of nuclides, and Isotope Lists. For a table see Table of Nuclides.

Gamma emission only

Isotope Activity Half-life Energies (keV)
Barium-133 9694 TBq/kg (262 Ci/g) 10.7 years 81.0, 356.0
Cadmium-109 96200 TBq/kg (2600 Ci/g) 453 days 88.0
Cobalt-57 312280 TBq/kg (8440 Ci/g) 270 days 122.1
Cobalt-60 40700 TBq/kg (1100 Ci/g) 5.27 years 1173.2, 1332.5
Europium-152 6660 TBq/kg (180 Ci/g) 13.5 years 121.8, 344.3, 1408.0
Manganese-54 287120 TBq/kg (7760 Ci/g) 312 days 834.8
Sodium-22 237540 Tbq/kg (6240 Ci/g) 2.6 years 511.0, 1274.5
Zinc-65 304510 TBq/kg (8230 Ci/g) 244 days 511.0, 1115.5
Technetium-99m 1.95×104 TBq/g (5.27 × 107 Ci/g) 6 hours 140

Beta emission only

Isotope Activity Half-life Energies (keV)
Strontium-90 5180 TBq/kg (140 Ci/g) 28.5 years 546.0
Thallium-204 17057 TBq/kg (461 Ci/g) 3.78 years 763.4
Carbon-14 166.5 TBq/kg (4.5 Ci/g) 5730 years 49.5 (average)
Tritium (Hydrogen-3) 357050 TBq/kg (9650 Ci/g) 12.32 years 5.7 (average)

Alpha emission only

Isotope Activity Half-life Energies (keV)
Polonium-210 166500 TBq/kg (4500 Ci/g) 138 days 5304.5
Uranium-238 12580 KBq/kg (0.00000034 Ci/g) 4.468 billion years 4267

Multiple radiation emitters

Isotope Activity Half-life Radiation types Energies (keV)
Caesium-137 3256 TBq/kg (88 Ci/g) 30.1 years Gamma & beta G: 32, 661.6 B: 511.6, 1173.2
Americium-241 129.5 TBq/kg (3.5 Ci/g) 432.2 years Gamma & alpha G: 59.5, 26.3, 13.9 A: 5485, 5443

Bioremediation

Lichens can accumulate radionuclides to a high level.[12]

See also

Notes

  1. R.H. Petrucci, W.S. Harwood and F.G. Herring, General Chemistry (8th ed., Prentice-Hall 2002), p.1025-26
  2. Eisenbud, Merril; Gesell, Thomas F (1997-02-25). Environmental Radioactivity: From Natural, Industrial, and Military Sources. p. 134. ISBN 9780122351549.
  3. Smoke Detectors and Americium
  4. Office of Radiation Protection – Am 241 Fact Sheet – Washington State Department of Health
  5. "Smoke Detectors: Uses of Radioactive Isotopes". Chemistry Tutorial : Radioisotopes in Smoke Detectors. AUS-e-TUTE n.d. Retrieved March 30, 2011.
  6. Reaction in a Smoke Detector
  7. PNNL: Isotope Sciences Program – Gadolinium-153
  8. "Gadolinium". BCIT Chemistry Resource Center. British Columbia Institute of Technology. Retrieved 30 March 2011.
  9. . World Health Organization http://www.who.int/mediacentre/factsheets/fs371/en/. Retrieved January 27, 2014. Missing or empty |title= (help)
  10. "Cosmic Detectives". The European Space Agency (ESA). 2013-04-02. Retrieved 2013-04-15.
  11. Table data is derived by counting members of the list; see WP:CALC. References for the list data itself are given below in the reference section in list of nuclides
  12. Gadd, G. M. (2009). "Metals, minerals and microbes: Geomicrobiology and bioremediation". Microbiology 156 (3): 609. doi:10.1099/mic.0.037143-0.

References

External links


This page was last modified on 16 March 2014 at 06:46.