色的珠宝和皮肤 - 一个微妙的外部标记,表明暴露于硫化
John D Gilbert1, Roger W Byard2,3
1Forensic Science SA, 21 Divett Place, Adelaide, 5000, Australia.
Forensic science, medicine, and pathology
|July 17, 2024
概括
硫化中毒导致一名妇女死亡,异常的大脑变色和色的银珠宝表明了这一点. 这种皮肤从银色变色可能是硫化暴露的微妙标记.
科学领域:
- 法医毒理学 法医毒理学
- 环境健康 环境健康
- 神经病理学神经病理学
背景情况:
- 硫化 (H2S) 是一种有毒气体,具有典型的腐蛋气味.
- H2S中毒可以通过各种暴露途径发生,包括吸入.
- 微妙的H2S暴露的外部标记在法医文献中并不成熟.
研究的目的:
- 报告一个致命的硫化中毒病例.
- 调查H2S暴露与外部物理发现之间的相关性.
- 在法医调查中突出显示H2S毒性的潜在诊断标记.
主要方法:
- 案例研究涉及一个已故的个人发现在车辆中怀疑H2S暴露.
- 尸体解剖检查包括毛病学和内部器官评估.
- 对化学反应的外部发现的分析,包括皮肤和珠宝.
主要成果:
- 死亡者脑灰质呈现绿色变色,这是一个独特的发现.
- 银饰品 (戒指和项链) 显示出黑色变色和相关的皮肤染色.
- 观察到的结果与硫化和银之间的化学反应一致.
结论:
- 死亡归因于硫化中毒.
- 绿色的大脑变色是H2S毒性的重要内部发现.
- 皮肤变色和色的银饰可能作为H2S暴露的微妙外部指标.
相关概念视频
Preparation and Reactions of Thiols
6.1K
Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol.
6.1K
Preparation and Reactions of Sulfides
4.8K
Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
4.8K
Structure and Nomenclature of Thiols and Sulfides
4.6K
Thiols and sulfides are sulfur analogs of alcohols and ethers, respectively, where the sulfur atom takes the place of the oxygen atom. Thus, thiols are generally represented as RSH, where R is an alkyl substituent and —SH is the functional group. On the other hand, in sulfides, the central sulfur atom is bonded to two hydrocarbon groups on either side. Depending upon the type of group, sulfides can be either symmetrical or asymmetrical. Both thiols and sulfides display a bent geometry,...
4.6K
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
1.8K
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
1.8K
Amines to Sulfonamides: The Hinsberg Test
3.3K
The Hinsberg test is a method to identify primary, secondary and tertiary amines, named after its pioneer, Oscar Hinsberg. Here, amines are treated with benzenesulfonyl chloride, also known as the Hinsberg reagent, in the presence of an excess of aqueous base, followed by acidification. Based on the nature of the amines, different changes are observed.
Generally, a primary amine reacts with the Hinsberg reagent to produce an N-substituted benzenesulfonamide. The electron-withdrawing...
Generally, a primary amine reacts with the Hinsberg reagent to produce an N-substituted benzenesulfonamide. The electron-withdrawing...
3.3K
Corrosion
24.0K
The degradation of metals due to natural electrochemical processes is known as corrosion. Rust formation on iron, tarnishing of silver, and the blue-green patina that develops on copper are examples of corrosion. Corrosion involves the oxidation of metals. Sometimes it is protective, such as the oxidation of copper or aluminum, wherein a protective layer of metal oxide or its derivatives forms on the surface, protecting the underlying metal from further oxidation. In other cases, corrosion is...
24.0K


