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Beryllium (Be), a lightweight metal with significant industrial applications, poses notable environmental and health risks due to its toxicity and persistence, and widespread use, particularly in the mechanical, aerospace, and electronics sectors. It is commonly alloyed with other heavy metals to enhance material properties. The primary environmental pathways for Be release include emissions from coal and fossil fuels combustion, as well as the incineration of solid wastes. Once introduced into the natural environment, primarily Be associated with soil particles and sediments, particularly in terrestrial and aquatic ecosystems. This review examined the pathways through which Be enters the environment, including atmospheric deposition, industrial discharge, and leaching from natural geologic deposits. The paper highlights the bioavailability and mobility of Be in soil and water systems, emphasizing the geochemical and physical factors influencing its persistence and potential for bioaccumulation. Risk appraisal methodologies are evaluated, with a focus on human exposure routes, including inhalation of airborne particulates and ingestion of contaminated water and food. The toxicological impacts on human health are critically analyzed, detailing both acute and chronic effects, such as respiratory diseases and carcinogenicity. This review evaluates existing regulatory frameworks and remediation strategies, assessing their efficacy in mitigating environmental contamination and exposure to Be. By integrating interdisciplinary research, this paper provides an in‐depth understanding of the environmental behavior and toxicology of beryllium, offering insights that can inform robust policy frameworks and shape future research directions.
Beryllium (Be), a lightweight metal with significant industrial applications, poses notable environmental and health risks due to its toxicity and persistence, and widespread use, particularly in the mechanical, aerospace, and electronics sectors. It is commonly alloyed with other heavy metals to enhance material properties. The primary environmental pathways for Be release include emissions from coal and fossil fuels combustion, as well as the incineration of solid wastes. Once introduced into the natural environment, primarily Be associated with soil particles and sediments, particularly in terrestrial and aquatic ecosystems. This review examined the pathways through which Be enters the environment, including atmospheric deposition, industrial discharge, and leaching from natural geologic deposits. The paper highlights the bioavailability and mobility of Be in soil and water systems, emphasizing the geochemical and physical factors influencing its persistence and potential for bioaccumulation. Risk appraisal methodologies are evaluated, with a focus on human exposure routes, including inhalation of airborne particulates and ingestion of contaminated water and food. The toxicological impacts on human health are critically analyzed, detailing both acute and chronic effects, such as respiratory diseases and carcinogenicity. This review evaluates existing regulatory frameworks and remediation strategies, assessing their efficacy in mitigating environmental contamination and exposure to Be. By integrating interdisciplinary research, this paper provides an in‐depth understanding of the environmental behavior and toxicology of beryllium, offering insights that can inform robust policy frameworks and shape future research directions.
Radioactive effluents, originating from nuclear power plants, medical‐nuclear applications, and various extraction industries worldwide, present a significant and dangerous contamination challenge. The concentrations of radioactive substances in wastewater, surface water, and potable water vary widely depending on the source and location. For example, cesium‐137 levels in wastewater from nuclear facilities can range from 0.1 to 10 Bq/L, while tritium concentrations in surface water near nuclear plants can reach up to 100 Bq/L. Regulatory guidelines, like the maximum contaminant level of 0.185 Bq/L for combined radium‐226 and radium‐228 in drinking water, are critical for ensuring safety and environmental protection. Specifically, in Fukushima, Japan, cesium‐137 levels in surface water range from 0.1 to 10 Bq/L due to the nuclear accident. In contrast, regions with natural uranium deposits, like parts of the United States, have reported radium‐226 concentrations in potable water up to 1 Bq/L. These variations highlight the necessity for focused monitoring and evaluation to protect water quality and community health. Among various methods, Gamma spectrometry and inductively coupled plasma mass spectrometry are precise for radionuclide quantification, scintillation detectors, and ion exchange, and adsorption techniques efficiently remove radioactive substances from water. This critical review examines the sources, adverse effects, and analysis and remediation strategies for various radioactive elements in wastewater. By thoroughly evaluating the origins and potential dangers associated with radioactive effluents, this report emphasizes the urgent need for rigorous monitoring and effective treatment practices to maintain the integrity of water resources and ecosystems.Practitioner Points Comprehensive analysis of the radioactive elements frequently found in wastewater and drinking water. Assess the negative effects of radioactive elements in water systems. Examine the treatment methods used to eliminate radioactive pollutants from water sources. Outline effective methods and tactics for addressing and controlling radioactive contamination occurrences. Analyze the latest advancements in technology, regulatory enhancements, and optimal methods to guarantee the safety of drinking water and the sustainable handling of radioactive substances in wastewater.
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