جدول المحتويات:
أندر عنصر على وجه الأرض (قد 2024)
أستاتين، عنصر كيميائي مشع وأثقل عضو في عناصر الهالوجين ، أو المجموعة 17 (VIIa) من الجدول الدوري. تم إنتاج Astatine ، الذي لا يحتوي على نظائر مستقرة ، لأول مرة صناعيًا (1940) في جامعة كاليفورنيا من قبل الفيزيائيين الأمريكيين ديل ر. كورسون ، كينيث ر. أستاتين 211 والنيوترونات. تم العثور على نظائر الأستاتين التي تحدث بشكل طبيعي في وقت لاحق بكميات دقيقة في سلسلة الاضمحلال الإشعاعي الطبيعية الثلاثة ، والتي تحدث فيها عن طريق التفرع الصغير (astatine-218 في سلسلة اليورانيوم ، astatine-216 في سلسلة الثوريوم ، و astatine-215 و astatine- 219 في سلسلة الأكتينيوم). اثنان وثلاثون نظيرًا معروفة ؛ astatine-210 ، مع نصف عمر 8.1 ساعات ، هو أطول عمر.نظرًا لأن الأستاتين لا يحتوي على نظائر مستقرة أو طويلة العمر ، فقد تم تسميته من الكلمة اليونانية astatos ، والتي تعني "غير مستقر".
الهالوجين
(Br) واليود (I) و astatine (At) و tennessine (Ts). أعطيت لهم اسم هالوجين ، من الجذور اليونانية hal- ("الملح")
خصائص العنصر
| العدد الذري | 85 |
|---|---|
| أكثر النظائر ثباتًا | 210 |
| الأكسدة | −1 ، +1 ، +3 (؟) ، +5 ، +7 (؟) |
| تكوين الإلكترون. | (Xe) 4f 14 5d 10 6s 2 6p 5 |
الإنتاج والاستخدام
الطريقة العملية الوحيدة للحصول على الأستاتين هي توليفها من خلال التفاعلات النووية. عادة ما يتم تحضير الأستاتين وفقًا للمعادلة العامة:
which indicates that bismuth-209 takes up one alpha particle and emits x neutrons to form an isotope of astatine, whose atomic weight depends on the number of neutrons lost. Metallic bismuth may be used as a target material. From this, astatine may readily be removed by distillation in air from a stainless-steel tube. The free element begins to distill at 271 °C (520 °F, or the melting point of bismuth), but the operation is best carried out at 800 °C (1,500 °F) with subsequent redistillation. If an aqueous solution of astatine is desired, the element may be separated by washing with an appropriate aqueous solution. Alternatively, the halogen may be removed from the target by chemical methods, such as dissolving in nitric acid, with the latter being removed by boiling.
Another procedure involves the use of a metallic thorium target, which—after bombardment—is dissolved in concentrated hydrochloric acid containing hydrogen fluoride and chlorine.
Analysis
Because of the short half-lives of astatine isotopes, only very small quantities have been available for study. With the exception of a few spectrometric and mass-spectrometric studies, most investigations of astatine chemistry have used tracer techniques, which involve using chemical reactions in a solution with similarly reacting elements as carriers. The amount of astatine is then calculated from the measured radioactivity of the reaction products. However, the rarity of astatine means that these solutions are extremely dilute, with concentrations around or below 10−10 molarity (the number of moles per litre of solution). At such concentrations, the effects of impurities can be very serious, especially for a halogen such as astatine, which exists in several oxidation states and can form many organic compounds. Iodine has been used as a carrier in most experiments. Techniques applied include coprecipitation, solvent extraction, ion exchange, and other forms of chromatography (separation by adsorption differences), electrodeposition (deposition by an electric current), electromigration (movement in an electric field), and diffusion. A direct identification of some astatine compounds has been made by mass spectrometry.
Except for nuclear properties, the only physical property of astatine to be measured directly is the spectrum of atomic astatine. Other physical properties have been predicted from theory and by extrapolation from the properties of other elements.
Chemical properties
Some of the chemical properties of the element have been established. It generally resembles iodine. Thus, like iodine, it concentrates in the thyroid gland of higher animals. A substantial portion, however, is distributed throughout the body and acts as an internal radiation source.
The astatide ion, At−, is quantitatively coprecipitated with insoluble iodides, such as silver iodide or thallium iodide. The diffusion coefficient of the iodide ion is 1.42 times that of the astatide ion, which moves more slowly toward the anode than the former under given conditions. The ion is formed by reduction of the element, using zinc or sulfur dioxide. It is oxidized to the zero valence state by the ferric ion, Fe3+, iodine (I2), and dilute nitric acid. Thus, the astatide ion is a stronger reducing agent than the iodide ion, and free iodine is a stronger oxidizing agent than astatine.
Free astatine is characterized by volatility from solution and by extractability into organic solvents. It undergoes disproportionation in alkaline media. Astatine is coprecipitated with cesium iodide and thus appears to form polyhalide anions. Astatine extracted into chloroform has been shown to coprecipitate homogeneously with iodine when a portion of the latter is crystallized. Astatine seems to be present as the iodide, which appears to be more polar (i.e., showing separation of electric charge) in character than iodine bromide. It is somewhat soluble in water and much more soluble in benzene and carbon tetrachloride.
Astatine is known to occur in positive oxidation numbers. The astatate ion, (AtO3)−, is coprecipitated with insoluble iodates, such as silver iodate (AgIO3), and is obtained by the oxidation of lower oxidation states with hypochlorite, periodate, or persulfate. So far no evidence for perastatate has been found, but this may be because the ion, (AtO6)5−, may show little tendency to coprecipitate with potassium iodate (KIO4).
Astatine in the +1 state is stabilized by complexation, and complexes formulated as dipyridine astatine perchlorate [At(py)2] [ClO4] and dipyridine astatine nitrate [At(py)2] [NO3] have been prepared. Compounds with the formulas (C6H5)AtCl2, (C6H5)2AtCl, and (C6H5)AtO2 have also been obtained. A variety of methods may be used to synthesize astatobenzene, C6H5At.
