Effect of fluoride on the amount of aluminium dissolved by boiling fruit acids

Boiling citric and tartaric acids dissolved aluminium from sheets and pans made of this metal. Fluoride increased the amount of aluminium dissolved by both citric and tartaric acids at the sort of concentrations which might be used in normal cookery (0.2%, pH 2.6). Increasing the amount of fluoride increased the amount of dissolved aluminium. The proportional increase was greater at low fluoride levels. Acids varied in their individual effects; tartaric acid dissolved considerably more aluminium than citric acid under any given set of conditions. The longer an acid solution was boiled with aluminium, the more of the metal dissolved. Repeated boiling of aluminium in acid solutions did not necessarily alter its response to further boiling. Old pans were attacked more strongly by acid solutions when fluoride was present. The precise composition of the aluminium metal used did not affect any of these conclusions.     

Fluoride in the prey of barn owls (Tyto alba)

Bone fluoride in short-tailed voles (Microtus agrestis) and common shrews (Sorex araneus), the prey of barn owls (Tyto alba), was studied on Anglesey, North Wales. The average fluoride content of M. agrestis skulls obtained from a location 0.9 km from an aluminium reduction plant was significantly greater than that of skulls from another location 22 km from the source of industrial fluoride pollution. At both locations, mean fluoride levels of skulls extracted from owl pellets and those of voles trapped mechanically were broadly similar but important differences existed. Near the aluminium reduction plant, owls caught voles and shrews with a much wider range of fluoride levels than occurred at a single trapping site. However, there was no evidence for selection of heavily fluoridated prey. Within 1 km of the aluminium reduction plant, six trapping sites yielded S. araneus with a fourfold difference between the highest and lowest mean bone fluoride level.     

Stabilization of FGD gypsum for its disposal in landfills using amorphous aluminium oxide as a fluoride retention additive

The applicability of amorphous aluminium oxide as a fluoride retention additive to flue gas desulphurisation (FGD) gypsum was studied as a way of stabilizing this by-product for its disposal in landfills. Using a batch method the sorption behaviour of amorphous aluminium oxide was evaluated at the pH (about 6.5) and background electrolyte conditions (high chloride and sulphate concentrations) found in FGD gypsum leachates. It was found that fluoride sorption on amorphous aluminium oxide was a very fast process with equilibrium attained within the first half an hour of interaction. The sorption process was well described by the Langmuir model, offering a maximum fluoride sorption capacity of 61.7 mg g(-1). Fluoride sorption was unaffected by chloride co-existing ions, while slightly decreased (about 20%) by competing sulphate ions. The use of amorphous aluminium oxide in the stabilization of FGD gypsum proved to greatly decreased its fluoride leachable content (in the range 5-75% for amorphous aluminium oxide doses of 0.1-2%, as determined by the European standard EN 12457-4 [EN-12457-4 Characterization of waste-leaching-compliance test for leaching of granular waste materials and sludges-Part 4: one stage batch test at a liquid to solid ratio of 10 l/kg for materials with particle size below 10mm (without or with size reduction)]), assuring the characterization of this by-product as a waste acceptable at landfills of non-hazardous wastes according to the Council Decision 2003/33/EC [Council Decision 2003/33/EC of 19 December 2002. Establishing criteria and procedures for the acceptance of waste at landfills pursuant to Article 16 of and Annex II to Directive 1999/31/EC] on landfill of wastes. Furthermore, as derived from column leaching studies, the proposed stabilization system proved to be highly effective in simulated conditions of disposal, displaying a fluoride leaching reduction value about 81% for an amorphous aluminium oxide added amount of 2%.     

The Effect of Rapid Transit on San Francisco Bay Air Quality

Classical procedures for the microdetermination of fluoride in vegetation are extremely time consuming. They generally involve ashing, fusion with alkali, distillation, and finally fluoride estimation. Sample size requirements for such procedures are on the order of a gram or more, making the procedure useless for determining low fluoride concentrations in small samples. A procedure for micro-fluoride determination in vegetation is proposed which utilizes the oxygen flask combustion technique (Schoniger flask). The gaseous products of combustion are absorbed in 10.0 ml of 0.05N sodium hydroxide containing 1.00 µg of fluoride. The analysis of the fluoride is performed directly on the absorption solution after addition of a combination complexing-buffer solution, using a specific fluoride ion electrode. The sensitivity of the electrode is such that 0.2 µg of fluoride can be easily detected in this volume. Added oxidant was required in the combustion step for some vegetation samples to completely free the fluoride from its organic matrix. Comparisons with the standard Willard-Winter procedure gave excellent results. Combustion of sodium fluoride standards as well as submicrogram quantities of a fluoro-organic compound showed recoveries greater than 90%. The direct combustion, coupled with fluoride ion electrode determination, reduces analysis time drastically. A complete analysis can be performed in 1/2 hr, with a minimum amount of equipment.     

A calcite permeable reactive barrier for the remediation of Fluoride from spent potliner (SPL) contaminated groundwater

The use of calcite (CaCO3) as a substrate for a permeable reactive barrier (PRB) for removing fluoride from contaminated groundwater is proposed and is illustrated by application to groundwater contaminated by spent potliner leachate (SPL), a waste derived from the aluminium smelting process. The paper focuses on two issues in the implementation of calcite permeable reactive barriers for remediating fluoride contaminated water: the impact of the groundwater chemical matrix and CO2 addition on fluoride removal. Column tests comparing pure NaF solutions, synthetic SPL solutions, and actual SPL leachate indicate that the complex chemical matrix of the SPL leachate can impact fluoride removal significantly. For SPL contaminant mixtures, fluoride removal is initially less than expected from idealized, pure, solutions. However, with time, the effect of other contaminants on fluoride removal diminishes. Column tests also show that pH control is important for optimizing fluoride removal with the mass removed increasing with decreasing pH. Barrier pH can be regulated by CO2 addition with the point of injection being critical for optimising the remediation performance. Experimental and model results show that approximately 99% of 2300 mg/L fluoride can be removed when CO2 is injected directly into the barrier. This can be compared to approximately 30-50% removal when the influent solution is equilibrated with atmospheric CO2 before contact with calcite.     

Phosphate removal from wastewater using aluminium oxide as adsorbent

The development and manufacture of an adsorbent to remove phosphate for the prevention of eutrophication in lakes is very important. The use of aluminium oxide (alumina) as an organic adsorbent to remove phosphate from wastewater has been investigated. The characteristics of this absorption process were investigated to determine the important parameters, such as the pH and the aluminium ion concentration. Moreover, chemical treatment methods to enhance the adsorption capacity of alumina were tested. Dynamic studies and equilibrium adsorption isotherm studies were conducted to determine the adsorption capacity and efficiency. The experimental results indicate that it is necessary to increase the temperature above 500°C in order to obtain a high-capacity adsorbent, and alumina treated with acid or calcium or magnesium has a larger adsorption capacity for phosphate than untreated adsorbent. Moreover, the adsorption of phosphate was enhanced at a lower pH and a higher aluminium ion concentration, and a simple Freundlich isotherm could express the equilibrium adsorption isotherm, and the intragranular diffusion controlling model was used to test the dynamic studies. These findings have important implications for the application and development of aluminium oxide as a prospective adsorbent.     

Factors determining amounts of fluoride in woodlice Oniscus asellus and Porcellio scaber, litter and soil near an aluminium reduction plant

Amounts of fluoride were measured in whole woodlice Oniscus asellus and Porcellio scaber, together with associated soil and litter, from 17 sites near an aluminium reduction plant at Holyhead, Anglesey, in North Wales. There was a strong positive correlation between amounts of fluoride in woodlice, soil and litter in all comparisons (P<0.02). Highest and lowest fluoride concentrations in woodlice differed by a factor of >50. Where both woodlice species occurred together at the more polluted sites, fluoride levels in Oniscus asellus were generally twice as high as those found in Porcellio scaber. At any given site, amounts of environmental fluoride were determined partly by distance and direction from the pot-rooms of the plant (a function of prevailing winds), modified by the presence of trees which acted as collectors for gaseous and particulate fluoride.     

A model describing the complexing effect in the leaching of aluminum from cooking utensils

A simple model describing the complexing effect in the leaching of aluminum from cooking utensils is presented in this paper. Some experimental results obtained by previous workers may be explained by this model, which demonstrates that the complexing effect takes a very important role in the process of aluminum liberated from cooking utensils. Increased concentrations of complexing ions (organic acids, fluoride ion, OH-, etc.) significantly enhance the release of aluminum. The speciation of aluminum in simulated food solution is also investigated. The model suggests that in the pH range of most food (pH 4-8) aluminum present is predominantly in the form of organic Al-complexes, which is harmful to the human body.     

诱导结晶法去除地下水中氟离子简

针对现行高氟地下水处理工艺中存在的工艺复杂、运行管理困难等问题，提出采用诱导结晶法除氟。其技术核心是在高氟水中投加氟磷灰石作为晶种，并投加磷酸盐和钙盐使水中氟离子在晶种表面生成氟磷酸钙（Ca₁₀（PO₄） ₆F₂）结晶。通过单因素实验得出最佳工艺条件：投加8g/L氟磷灰石，并投加NaH₂PO₄和CaCl₂，使钙离子、磷酸根离子和氟离子的摩尔比为10：5：1，搅拌速度为100 r/min，反应时间1 h。反应中磷酸根离子和钙离子的利用率分别达到98%和25%以上。电子扫描显微镜（SEM）表征晶种在参与反应后，表面有结晶生成。研究表明，采用诱导结晶法可将水中氟离子浓度从5~10 mg/L降至1 mg/L以下，达到饮用水水质标准。     

含氟离子和氯离子酸性废水处理技术

本实验研究了石灰乳和铝酸钠处理废水中的氟离子和氯离子的效果。通过正交实验得出:影响除氟离子效果因素的主次顺序为:pH值>氟离子浓度>反应时间;影响除氯离子效果因素的主次顺序为:氯离子浓度>铝酸钠与氯离子的质量浓度比>反应时间。通过单因素实验得出:在pH=9、反应时间为5 min的条件下,废水中氟离子含量可由370.37mg/L降低到2 mg/L以下,去除率可达99.45%;在铝酸钠与氯离子的质量浓度比为1∶10,反应时间为5 min的条件下,废水中氯离子含量可由503.4 mg/L降低到201 mg/L以下,去除率可达60%。     

Effects of airborne fluoride emissions near an aluminium works in Wales: part 2--saxicolous lichens growing on rocks and walls

Effects of fluoride (F(-)) emissions on previously unpolluted assemblages of saxicolous lichens, near an aluminium reduction works, are described. Lichens contained a mean 16 microg F(-) g(-1) dry weight in 1970 before emissions commenced. Subsequently, where annually monitored Ramalina contained >100microg g(-1) severe damage occurred, including loss of attachment to the rocky substratum. At sites within 1 km of the works well-exposed to emissions, fruticose (shrubby) lichens were eliminated, but in more sheltered locations 18% cover had survived by 1983. Some foliose (leaf-like) lichens tolerated >200 microg g(-1), while crustose (crust-like) species were least affected, 32% and 70% surviving, respectively. Concentrations of fluoride, and associated injury, decreased with increasing distance from the works. Fruticose and sensitive foliose species sustained 40-75% losses of cover up to 4 km NE, downwind of the works, where fluoride averaged 50-100 microg g(-1), but <40% losses were recorded in fruticose species up to 9 km, where concentrations averaged 35-50 microg. Saxicolous lichens were damaged less than corticolous species previously reported and, following decreased emissions, were also regrowing in sheltered and more distant locations by 1985.     

氯化镁复配硫酸铝混凝性能及絮体特性

在研究氢氧化镁混凝特性的基础上,复配氯化镁和硫酸铝作为混凝剂,以高岭土配水水样为研究对象,运用iPDA在线监测技术对混凝过程絮体形成进行监测,探讨了单独使用氯化镁和硫酸铝以及二者复配使用的混凝效果和絮体特性,确定复配使用的各种条件。结果表明,对于浊度20 NTU,pH 11.5的高岭土配水水样,氯化镁、硫酸铝最佳投加量分别为7.2 mg/L(Mg2+计)和3 mg/L(Al3+计);硫酸铝跟氯化镁复配使用时,先投加硫酸铝,间隔30 s后投加氯化镁,混凝效果较好;在镁离子最佳投加量7.2 mg/L时,铝和镁最佳质量比在1∶3~1∶2之间;镁铝复配时其FI值明显大于单独作用时,即絮体尺寸大小:二者复配硫酸铝氯化镁,而且复配条件下Zeta电位值在零电势左右浮动,浮动范围小,更利于聚集沉淀;镁铝复配时发生了协同效应,弥补了单独使用氯化镁混凝过程的不足。     

Air Quality Standards for Fluoride Vegetation Effects

Facts that must be taken into consideration in developing fluoride standards for vegetation effects include: (1) Fluoride is an accumulative toxicant and injury is usually associated with long-term exposure; (2) gaseous and particulate fluorides differ in their phytotoxicity; (3) plant species and varieties differ greatly in susceptibility to fluoride; (4) extremely low concentrations can cause damage to sensitive species. Three possible approaches to standards are discussed: Atmospheric fluoride concentration, vegetation fluoride concentration, and the presence of leaf necrosis or chlorosis. Atmospheric fluoride concentration has the advantage that it fits the conventional concept of standards and that it is objective. Accurately measuring low fluoride concentrations, separating gaseous from particulate fluorides in the air sample, and establishing a safe concentration present technical problems, however. Vegetation analysis may more closely represent fluorides available to affect the plant. The presence of significant amounts of fluoride-induced leaf necrosis (e.g., 3% of the leaf area) may be the most practical approach to standards for fluoride vegetation effects. Advantages are that the combined effects of the forms of fluoride, species and varieties, and concentration-time relationships are all manifest in the factor that is measured. Relatively little time is required to examine the vegetation in a large area and only 2 or 3 surveys a year are required.     

Status of industrial fluoride pollution and its diverse adverse health effects in man and domestic animals in India

Hydrofluorosis in humans and domestic animals is a worldwide health problem and caused by a prolonged period of fluoride exposure through drinking of fluoride contaminated water. But in recent years, due to rapid industrialization in India, diverse serious health problems among industrial workers and residents and domestic animals living in the industrial areas due to fluoride pollution are on the rise. A number of coal-burning and industrial activities such as power-generating stations, welding operations and the manufacturing or production of steel, iron, aluminum, zinc, phosphorus, chemical fertilizers, bricks, glass, plastic, cement, and hydrofluoric acid are generally discharging fluoride in both gaseous and particulate/dust forms into surrounding environments which create a industrial fluoride pollution and are an important cause of occupational exposure to fluoride in several countries including India. An industrial emitted fluoride contaminates not only surrounding soil, air, and water but also vegetation, crops and many other biotic communities on which man and animals are generally dependants for food. Long- time of inhalation or ingestion of industrial fluoride also causes serious health problems in the forms of industrial and neighborhood fluorosis. In India, whatever research works conducted so far on the chronic industrial fluoride intoxication or poisoning (industrial and neighborhood fluorosis) in man and various species of domestic animals due to a prolonged period of industrial fluoride exposure or pollution (contamination) are critically reviewed in the present communication. Simultaneously, we are also focused the various bio-indicators and bio-markers for chronic industrial fluoride intoxication or pollution.     

Human exposure to fluoride from tea (Camellia sinensis) in a volcanic region—Canary Islands,Spain

Fluoride is highly present in the environment, especially in water and its derivatives. Excessive fluoride contribution to diet poses a health risk. Tea leaves accumulate fluoride and the consumption of tea (Camellia sinensis) could pose a risk to human by the excessive fluoride intake. Ninety tea samples were analyzed by potentiometry using a selective fluoride ion electrode. Mixed tea samples (2.82?±?1.11 mg/L) and black tea samples (2.28?±?0.79 mg/L) recorded the highest fluoride levels. The contribution of drinking water is important for increasing fluoride levels in teas. The daily consumption of two cups (250 mL per cup) of mixed and black teas prepared with La Laguna tap water does pose a health risk for children (4–8 years old) because of the high contribution percentages (74.4% and 63.6%, respectively) of the Tolerable Upper Intake Level set in 2.5 mg/day by the EFSA (European Food Safety Authority). A minor consumption in children (4–8 years old) and adults during pregnancy is advisable.

     

Removal of fluoride from water by using a coagulant (inorganic polymeric coagulant)

Environmental Science and Pollution Research - Excess fluoride (F) ion of drinking water is a major problem in many areas of India and causes harmful effects such as dental and skeletal fluorosis....     

Fluoride deposition in snow in the surroundings of a mixed fertilizer factory

The fluoride content of snow was determined at various distances from a mixed fertilizer factory in Siilinjärvi, central Finland. Elevated fluoride levels were observed at less than 2 km from the factory, and the highest concentrations close to the factory were about 600 μg of fluoride per liter of melt water. At unpolluted reference sites the fluoride content was about 6μg/1. The background level of fluoride in precipitation is discussed. An ion selective electrode and a simple calibration method were used in the analyses.     

Light-induced degradation of perfluorocarboxylic acids in the presence of titanium dioxide

The UV-photon-induced degradation of heptafluorobutanoic acid was investigated in acidic aqueous solutions in the presence of titanium dioxide. Heptafluorobutanoic acid could be degraded with this photocatalyst in a light-induced reaction generating carbon dioxide and fluoride anions. Carbon dioxide evolution in a significant amount occurred only in the presence of molecular oxygen and the photocatalyst. The light-induced degradation of trifluoroacetic acid, pentafluoropropanoic acid, nonafluorobutanoic acid, pentadecafluorooctanoic acid, nonafluorobutanesulfonic acid, and heptadecafluorooctanesulfonic acid in the presence of titanium dioxide was also studied. The perfluorocarboxylic acids under investigation are degraded to generate CO(2) and fluoride anions while both perfluorinated sulfonic acids are persistent under the experimental conditions employed in this study. For all compounds photonic efficiencies of the mineralization reaction were estimated to be smaller than 1x10(-5). To increase the photocatalytic activity mixed systems containing homogeneous phosphotungstic acid and heterogeneous titanium dioxide catalysts were also investigated. In the mixtures of these two photocatalysts, the formation rate of CO(2) increased with illumination time.     

三维电极电吸附动态反应器的除氟特征研究

采用自制的单极性复合型三维阳极作为第三维电极对含氟水进行动态电促吸附实验,通过研究不同填充床高度、阴阳极板间距、隔膜材料对电促吸附除氟效果的影响,确定反应器的最佳结构参数为:填充床高度20 cm、阴阳极板间距4 cm、隔膜为nafion117膜。工作电压、进水pH、进水流速、共存物质对氟离子去除效果的影响结果表明:在一定范围内增大工作电压,降低进水pH或进水流速均可提高除氟效果。相应的最佳操作条件为:工作电压7 V、进水流速4 mL/min、酸性pH;腐殖酸和碳酸根离子的存在会对氟离子去除产生较强抑制作用,低浓度的氯离子可促进氟离子的电促吸附。扫描电镜(SEM)-电子能谱(EDX)的表征结果显示三维颗粒电极的表面及孔隙内部均可吸附氟离子,且电吸附后并未出现电极腐蚀现象。     

Studies on the acute toxicity of fluoride ion to stickleback,fathead minnow,and rainbow trout

We have studied the acute toxicity of fluoride ion to $\text{Gasterosteus aculeatus}$, $\text{Pimephales promelas}$, and juvenile $\text{Salmo gairdneri}$. LC50 values varied with species and (due to precipitation) initial water hardness. Exposure to elevated fluoride levels in water resulted in increased blood fluoride levels in $\text{Salmo gairdneri}$.