Microbiological profile of crude oil in storage tanks

Microbiological quality of crude oil storage tanks was determined. The samples were taken from crude oil storage tanks in three stations, at Ughelli, Escravos and Forcados tank farms in the Delta State of Nigeria. Two tanks were sampled at each station with samples collected from three levels of the tank, namely the oil layer, oil water interface, and effluent layer. Samples from the inner walls and bottom sediment of the only empty tank in Ughelli during the study were also taken. The total heterotrophic count of bacteria and total fungal count were obtained by plating samples on nutrient agar and sabouraud's glucose agar respectively and incubated for 14 days at 28 °C±2 °C. Oilutilizing bacteria and fungi were isolated on oil agar using fungizone and antibiotics to inhibit fungal and bacterial growth respectively. Pure cultures of bacteria and fungi were prepared on nutrient agar and sabouraud's glucose agar respectively at 28 °C±2 °C for 4 days. Isolates were identified using approved standard methods. Three bacterial genera, Pseudomonas, Proteus and Bacillus, and one actinomycete, Actinomyces and two fungal genera, Penicillium and Cunninghamella, were isolated. Pseudomonas was dominant among the bacteria (41.62%) and Penicillium dominant among the fungi (94%). It was also found that the total microbial load of the effluent layer was higher than that of the oil layer.     

Extractable Hydrocarbons, Nickel and Vanadium Contents of Ogbodo-Isiokpo Oil Spill Polluted Soils in Niger Delta, Nigeria

An oil spill polluted site at Ogbodo-Isiokpo in Ikwere Local Government Area of Rivers State in southern Nigeria, was identified for study following three successive reconnaissance surveys of oil fields in the Agbada west plain of Eastern Niger Delta. A sampling area of 200 m × 200 m was delimited at the oil spill impacted site using the grid technique and soils were collected at surface (0–15 cm) and subsurface (15–30 cm) depths from three replicate quadrats. A geographically similar, unaffected area, located 50 m adjacent to the polluted site, was chosen as a control (reference) site. Total extractable hydrocarbon contents of the polluted soils ranged from 3.02–4.54 and 1.60–4.20 mg/kg (no overlap in standard errors) at surface and subsurface depths respectively. The concentrations of two “diagnostic” trace heavy metals, nickel (Ni) and vanadium (V), which are normal constituents of crude oil, were also determined in the soils by atomic absorption spectrophotometric method after pre-extraction of cations with dithionite–citrate carbonate. Ni varied from 0.15 to 1.65 mg/kg in the polluted plots and from 0.18 to 0.82 mg/kg in the unpolluted plots; vanadium varied from 0.19 to 0.70 mg/kg in the polluted plots and from 0.14 to 0.38 mg/kg in the unpolluted plots. Ni and V were more enhanced (p < 0.05) in the oil-polluted soils, especially at subsurface depth. Whilst the oil spillage could be said to be indirectly responsible for the enhanced concentrations of nickel and vanadium via the injection and availability of the petroleum hydrocarbons that might have increased the activities of biodegradation on site, the physico-chemical properties of the soils and inherent mobility of metals, as well as the intense rainfall and flooding that characterized the period of study, may have also contributed, at least in part, to these enhanced concentrations. Such levels of Ni and V may result to enhanced absorption by plants, which may bring about possible bioaccumulation in such plants and the animals that depend on them for survival and all of these may lead to toxic reactions along the food chain.     

Effect of Temperature on Absorption Efficiency of NO2 in Arsenite Method

The sodium arsenite method developed by Jacobs andHochheiser is one of the most widely used manualmethods for nitrogen dioxide (NO₂) monitoring inambient air, particularly in developing countries. Asreported, the method gives 82% NO₂ absorptionefficiency (NAE) in the concentration range from 40 to750 g/m³, when only one impinger tube isemployed in the sampling train at a flow rate of 0.2lpm and for 24 h sampling duration. Accordingly,a uniform correction factor (0.82) is used indenominator to calculate the ultimate concentration ofNO₂ in ambient air.In the present investigation, the effect oftemperature on absorption efficiency of NO₂ isstudied employing four impinger tubes in series tocollect the maximum NO₂ generated in the gasstream. The study conducted at 16, 26 and 36 °Ctemperatures shows maximum absorption efficiency(average) of 87.8% at 26°C in 1st impingertube. At lower and higher temperatures, it is foundconsiderably less. A suitable correction factor,therefore, must be applied to estimate actual NO₂concentration in ambient air using arsenite method, intropical countries like India, where atmospherictemperature variations are large (less than 5°Cin winter and more than 45°C in summer).     

An Assessment of the Effects of Crude Oil Pollution on Soil Properties, Germination and Growth of Maize (Zea Mays) using Two Crude Types – Forcados Light and Escravos Light

The effect of crude oil pollution on soil properties, germination and height of maize (Zea mays) was investigated under natural environment in three separate pot experiments. Two crude oil types--Forcados light and Escravos light were used. In Experiment 1, the effect of crude oil application on germination using high pollution levels of 5, 15, 25 and 40 mL kg(-1) of soil was assessed. In Experiment 2, the effect of crude oil application on maize plant height using the same pollution levels was assessed. The last experiment (Experiment 3) was used to test for the effects of crude oil application on maize plant height using lower levels of pollution (1.0, 1.5, 2.0 and 2.5 mL kg(-1) of soil). Soil samples were collected before, during and after the experiment and analyzed for some physical and chemical properties. Results obtained showed variation in chemical properties of soil. % organic matter increased from 1.34 to 2.62% in polluted soils. Available P decreased from 15.00 ppm in control to between 7.34 and 5.42 in soils polluted with 'high' levels of crude oil. Statistical analysis of height data showed that crude oil inhibited the growth of maize at high pollution levels. High levels of pollution also inhibited germination and for Escravos light there was no germination at 40 mL kg(-1) soil level of crude oil pollution.     

A simple extraction procedure for determination of total mercury in crude oil

The determination of mercury in crude oil and petroleum products is particularly difficult due to the volatile nature of both mercury and the matrix, which may lead to significant loss of the analyte. A simple extraction method for total mercury has been developed to determine total mercury in crude oil using cold vapor atomic fluorescence spectrometry. The homogenized crude oil sample was diluted to 5, 10, and 20 % (w/w) in toluene. The diluted crude oil samples were spiked with 10 and 40 μg/kg (w/w). The samples were extracted using an oxidant/acid solution, BrCl/HCl. The mercury was extracted into the aqueous phase; the ionic mercury was then reduced to volatile elemental mercury (Hg⁰) by stannous chloride (SnCl₂). The mercury vapor was detected by Merlin cold vapor atomic fluorescence spectrometry at a 253.7-nm wavelength. The average recoveries for mercury in spiked diluted crude oil (10 and 40 μg/kg, w/w) were between 96 and 103 %, respectively, in 5 and 10 % spiked diluted crude oil. Whereas, low recoveries (<50 %) were recorded in 20 % diluted spiked crude oil. The method detection limit was calculated as t _{(0.01)(n ? 1)}?×?SD where t is the student's value for 99 % confidence level and standard deviation estimate with n???1 degrees of freedom. The method detection limit was found to be 0.38 μg/kg based on 5 g of diluted crude oil sample. The method is sensitive enough to determine low levels of mercury in crude oil.     

Exposure of Marine Mammals to Genotoxic Environmental Contaminants: Application of the 32P-Postlabeling Assay for Measuring DNA-Xenobiotic Adducts♯

There is little information on exposure of marine mammals to genotoxic environmental contaminants. The 32P-postlabeling assay has been successfully used to assess exposure to genotoxic polycyclic aromatic compounds in fish and humans. In the present study, a preliminary investigation showed that polycyclic aromatic compound-like DNA adducts were present in hepatic tissues of harbor seals (Phoca vitulina richardsi) exposed to petroleum following the Exxon Valdez oil spill. However, for marine mammals, effects from changes in tissue condition on DNA recovery and quality is of concern, because tissue samples are often collected from animals that have been dead for unknown periods of time. To assess the effects of postmortem thermal history on DNA recovery from tissue and on DNA adduct quantitation, samples of harbor porpoise (Phocoena phocoena) hepatic tissue were incubated for up to 10 d at 4 and 30 °C. Only traces (<4 g) of hepatic DNA were recovered from 200 mg of tissue after incubation at 30 °C for 36 h. At 4 °C, DNA (50–130 g) was recovered from tissue incubated for up to 6 d; whereas DNA recovery at 10 d was minimal. Chromatograms of 32P-labeled DNA digests of liver tissue held at 4 and 30 °C and salmon sperm DNA held at 30 °C for 2 d had comparable profiles, suggesting that alteration of DNA bases had occurred during incubation of porpoise liver tissue. Moreover, the chromatograms of DNA extracted from liver tissues of harbor porpoises caught incidentally in a northwest Atlantic fishery, packed in ice and sampled several days later also exhibited similar altered DNA structures. Although, altered DNA structures that can interfere with the DNA adduct quantitation were present in autolyzed tissue, changes in the 32P-postlabeling chromatography conditions can decrease the interference. Moreover, in a study with tissues taken from California sea lions (Zalophus californianus) immediately postmortem and stored at –80 °C until processing, DNA structures associated with tissue breakdown were not observed. The DNA from sea lions, however, had putative age-dependent hepatic DNA modifications, which have a distinctive profile, and must be considered when evaluating exposure of marine mammals to polycyclic aromatic compounds. Overall, the findings showed that with attention to the postmortem thermal history of the tissue samples hepatic DNA adducts, as measured by 32P-postlabeling, have the potential to serve as a biological indicator of exposure of marine mammals to environmental genotoxic compounds.     

Relative Phytoplankton growth responses to physically and chemically dispersed South Louisiana sweet crude oil

We conducted controlled laboratory exposure experiments to assess the toxic effects of water-accommodated fractions (WAFs) of South Louisiana sweet crude oil on five phytoplankton species isolated from the Gulf of Mexico. Experiments were conducted with individual and combinations of the five phytoplankton species to determine growth inhibitions to eight total petroleum hydrocarbon (TPH) equivalent concentrations ranging from 461 to 7,205 ppb. The composition and concentration of crude oil were altered by physical and chemical processes and used to help evaluate crude oil toxicity. The impact of crude oil exposure on phytoplankton growth varied with the concentration of crude oil, species of microalgae, and their community composition. At a concentration of TPH <?1,200 ppb, dinoflagellate species showed significantly better tolerance, while diatom species showed a higher tolerance to crude oil at higher concentrations of TPH. For both groups, the larger species were more tolerant to crude oil than smaller ones. The toxicity potential of crude oil seems to be strongly influenced by the concentration of polycyclic aromatic hydrocarbons (PAHs). The addition of the dispersant, Corexit® EC9500A, increased the amount of crude oil up to 50-fold in the water column, while the physical enhancement (vigorous mixing of water column) did not significantly increase the amount of TPH concentration in the water column. The species response to crude oil was also examined in the five-species community. Each phytoplankton species showed considerably less tolerance to crude oil in the five-species community compared to their individual responses. This study provides baseline information about individual phytoplankton responses to crude oil and dispersed crude oil for subsequent research efforts seeking to understand the impacts of oil on the phytoplankton in the bigger picture.     

Assessment of the Heavy Metal Pollution Effects on the Soil Respiration in the Baix Llobregat (Catalonia, NE Spain)

A main goal of investigations is to determine could a soilrespiration be an indicator of the soil pollution. In this case a measured levelof the soil oxygen consumption depends of its pollution. It alsomeans that the pollution reduces biological processes in edaphon.Investigated soil samples were taken from polluted andnon-polluted places in the Baix Llobregat near Barcelona (Catalonia, NE Spain). Soil samples were taken from the top ofsoil (0–5 cm) without a litter. Soil analysis were done, determining percentage shares of coarsefragments, coarse sand, fine sand, coarse silt, fine silt, clay,CaCO₃, organic matter as well as water pH and conductivityCE (1:5 [mS cm^-1]). Also were determined (in mg kg^-1)quantities of heavy metals, as Fe, Al, Mn, Zn, Cr, Ni, V, Cu, Cd, Pb.The soil respiration was investigated in temperatures15 and 30 °C and with controlled humidity.The respiration in 30 °C is number of times greater thenin 15 °C both for polluted and non-polluted soils.Particularly high coefficients of correlation between the soilrespiration and soil pollution in polluted soils were obtainedfor Pb: r = 0.75 in 15 °C and r = 0.98 in30 °C; for Ba: 0.90 and 0.57; for V: 0.99 and 0.81. In non-polluted soils highest correlation coefficients are for Pb: r = 0.70 in 15 °C; Fe: 0.60 and 0.72; Al: 0.68 and0.64; Mn: 0.51 and 0.66; Ba: 0.63 and 0.61; Cr: 0.94 and0.70; Ni: 0.64 and 0.65; Cu: 0.69 and 0.48; as well as V: 0.62in 15 °C; and Cd: 0.69 in 15 °C.This way the soil respiration could be a good indicator of the soil pollution.     

Comparison of wood-dust aerosol size-distributions collected by air samplers

A method has been described previously for determining particle size distributions in the inhalable size range collected by personal samplers for wood dust. In this method, the particles collected by a sampler are removed, suspended, and re-deposited on a mixed cellulose-ester filter, and examined by optical microscopy to determine particle aerodynamic diameters. This method is particularly appropriate to wood-dust particles which are generally large and close to rectangular prisms in shape. The method was used to investigate the differences in total mass found previously in studies of side-by-side sample collection with different sampler types. Over 200 wood-dust samples were collected in three different wood-products industries, using the traditional 37 mm closed-face polystyrene/acrylonitrile cassette (CFC), the Institute of Occupational Medicine (IOM) inhalable sampler, and the Button sampler developed by the University of Cincinnati. Total mass concentration results from the samplers were found to be in approximately the same ratio as those from traditional long-term gravimetric samples, but about an order of magnitude higher. Investigation of the size distributions revealed several differences between the samplers. The wood dust particulate mass appears to be concentrated in the range 10-70 aerodynamic equivalent diameter (AED), but with a substantial mass contribution from particles larger than 100 microm AED in a significant number of samples. These ultra-large particles were found in 65% of the IOM samples, 42% of the CFC samples and 32% of the Button samples. Where present, particles of this size range dominated the total mass collected, contributing an average 53% (range 10-95%). However, significant differences were still found after removal of the ultra-large particles. In general, the IOM and CFC samplers appeared to operate in accordance with previous laboratory studies, such that they both collected similar quantities of particles at the smaller diameters, up to about 30-40 [micro sign]m AED, after which the CFC collection efficiency was reduced dramatically compared to the IOM. The Button sampler collected significantly less than the IOM at particle sizes between 10.1 and 50 microm AED. The collection efficiency of the Button sampler was significantly different from that of the CFC for particle sizes between 10.1 and 40 microm AED, and the total mass concentration given by the Button sampler was significantly less than that given by the CFC, even in the absence of ultra-large particles. The results are consistent with some relevant laboratory studies.     

Thermal volatilization properties of atmospheric nanoparticles

Thermal volatilization is explored as a means of inferring the chemical composition of atmospheric aerosol particles with diameters smaller than 10 nm (nanoparticles). Such particles contain too little mass for quantitative chemical determination by traditional analytical methods. Aerosols were subjected to increasing temperature in an oven and particle loss was measured as a function of temperature with the TSI model 3025 ultrafine condensation particle counter (UCPC), which is capable of counting particles with diameters as small as 3 nm. Particle nucleation was observed down stream of the oven when it was heated above about 400°C. To reduce this artifact, the sample air down stream of the oven was cooled to condense the hot gases and/or the freshly nucleated particles before they reached the UCPC. Controlled experiments were done with pure ammonium sulfate (NH₄)₂SO₄ particles. The experimental design was optimized based on the known concentration of pure (NH₄)₂SO₄ particles vaporized in the oven and the diffusion of this material to the walls of the sampling tube before the particle counter.     

Operational problems related to the preparation of the seawater soluble fraction of crude oil

Owing to the importance of dissolution and weathering processes following oil spills, this work focused on the operational (quantitative) aspects related to the dissolution of petroleum-derived products, as well as the influence of solar light on both dissolution and the photoproduction of hydrogen peroxide. Four Brazilian crude oil samples were used to study the transfer process of organic compounds from the crude oil film to the aqueous phase (natural seawater) over a period of up to 45 days. Dissolved organic carbon (DOC), measured by non-dispersive infrared spectroscopy followed by high temperature catalytic combustion, was used to follow the partitioning between the two phases. Aqueous DOC values increased as a function of time (up to 15 days) until equilibrium was reached at concentrations ranging from 5 to 45 mg C L(-1). The final DOC concentration as well as the rate of dissolution depends on the nature of the crude oil. When exposed to sunlight, the dissolution was enhanced by up to 67.3%, and inorganic peroxides were generated in the concentration range from 4.5 up to 8.0 micromol L(-1) after 7.3 h irradiation. These results indicate that there is a need for a standard procedure for the production of the WSF in order to generate a more reliable tool to assess the impact of oil spills on the marine environment.     

Factors affecting the leaching of lead from UPVC pipes

This paper summarizes the results of a series of studies on the various factors that affect the leaching of lead from unplasticized poly(vinyl chloride) (UPVC) pipes. Factors that were studied include temperature, pH and extractants. Results showed that, for a given UPVC pipe, the rate of leaching of lead depended primarily on temperature and the nature of extractants. While the rate of leaching of lead was quite low with distilled water, it was very much enhanced by the presence of low concentration of anions such as Cl^-, HPO _inf4 ^sup2- HCO _inf3 ^sup- , NO _inf3 ^sup- , SO _inf4 ^sup2- and EDTA. EDTA, being a strong complexing agent, was most effective. Rates of leaching were found to be higher at elevated temperature except in the cases of HPO _inf4 ^sup2- and EDTA. Effect of pH was not pronounced. The temperature at which the UPVC pipes were extruded was found to affect the rate of leaching of lead. Pipes extruded at 190°C were found to have lower rate of leaching than those extruded at 180°C and 170°C. Analysis of the pipes by Scanning Electron Microscopy showed that the distribution of lead in the pipes extruded at 190°C was more uniform than those extruded at 170°C.     

湿法脱硫后高湿烟气中SO3酸雾监测方法研究

利用三氧化硫(SO3)发生装置以及模拟烟气湿法脱硫系统,研究了烟气再热温度、恒温水浴温度、采样速率、冷凝管类型规格及吸收瓶个数等不同采样参数对SO3酸雾采集率的影响。结果表明,当烟气再热温度低于烟气酸露点时会导致SO3酸雾收集率下降,采用控制冷凝法采样时应使用大流量(10L/min)采样,冷凝管应选择外套长度为400 mm的蛇形螺旋冷凝管,并将冷凝管置于温度为65℃左右的恒温水浴中;用碱液吸收法采样时应串联3个吸收瓶后,使用小流量(1L/min)采样。烟气温湿度、二氧化硫(SO2)浓度以及烟气中共存组分等对碱性吸收法的采集影响较大,而对控制冷凝法几乎没有影响。因此确立了针对湿法脱硫后高湿烟气环境下SO3酸雾的监测方法为控制冷凝法更为适宜。     

Simulation of the migration and transformation of petroleum pollutants in the soils of the Loess plateau: a case study in the Maling oil field of northwestern China

We developed a coupled water–oil simulation model to simulate the migration and transformation of petroleum-derived contaminants in the soil of the Xifeng oil field. To do so, we used the HYDRUS-2D model, which simulates the diffusion, adsorption or desorption, and microbial degradation of petroleum-derived hydrocarbons in the soil–water system. The saturated soil hydraulic conductivity of petroleum-derived pollutants was 0.05 cm?day^?1, which is about 1 to 2 % of the soil moisture permeability coefficient. Our numerical simulation results show that spilled crude oil was mainly concentrated in the surface horizons of the soil. The organic pollutant concentration tended to be highest nearest to the pollution source. The pollutant migration was generally concentrated within the top 20 to 30 cm of the soil, with the maximum concentration in the top 5 cm of the soil. With passing time, the pollutant accumulation increased and the adsorption and degradation functions reached a dynamic balance with the input rate at depths greater than 30 cm below the soil surface. The oil-derived pollutants totaled 50 to 100 mg?kg^?1 under the dynamic balance condition, which occurred after 20 to 30 years. The petroleum-derived pollutant concentration in the loess soil was inversely correlated with the horizontal distance from the oil well, and the concentration decreased greatly at a distance greater than 40 m from the well.     

Modeling trihalomethane formation for Jabal Amman water supply in Jordan

A mathematical model that expresses Total trihalomethane (TTHM) concentration in terms of initial chlorine concentration, total organic carbon, bromide ion concentration, contact time, and pH is developed for Zai water treatment plant which supplies water to Jabal Amman. The developed mathematical model is for constant temperature of 20°C. To adjust model calculated TTHM concentrations for temperatures other than 20°C, another mathematical model that expresses TTHM growth rate as function of temperature is also developed. To test the ability of the two developed models in predicting TTHM concentrations throughout water supplies, a sampling program that aimed at measuring TTHM concentrations in addition to the predictors in the two developed mathematical models namely; chlorine concentration, bromide ion concentration, total organic carbon, temperature and pH throughout Jabal Amman water supply was conducted. The two developed mathematical models and WaterCad, which was used to determine water age, were used to predict TTHM concentrations throughout Jabal Amman water supply. Predicted TTHM concentrations were compared to actual TTHM concentrations measured during the sampling program. Results showed that there is good agreement between measured and, calculated TTHM concentrations, which means that the method presented in this paper, can be used to obtain good estimates of TTHM concentrations throughout networks.     

Metal release from stainless steel particles in vitro-influence of particle size

Human inhalation of airborne metallic particles is important for health risk assessment. To study interactions between metallic particles and the human body, metal release measurements of stainless steel powder particles were performed in two synthetic biological media simulating lung-like environments. Particle size and media strongly influence the metal release process. The release rate of Fe is enhanced compared with Cr and Ni. In artificial lysosomal fluid (ALF, pH 4.5), the accumulated amounts of released metal per particle loading increase drastically with decreasing particle size. The release rate of Fe per unit surface area increases with decreasing particle size. Compared with massive sheet metal, fine powder particles (<4 microm) show similar release rates of Cr and Ni, but a higher release rate of Fe. Release rates in Gamble's solution (pH 7.4), for all powders investigated, are significantly lower compared to ALF. No clear trend is seen related to particle size in Gamble's solution.     

Status and Trends of Dissolved Oxygen in Corpus Christi Bay, Texas, U.S.A.

The purpose of this studywas to determine status and long-term trends of dissolved oxygen concentrations (DO) in Corpus Christi Bay, Texas, U.S.A. A 20-year record of randomized stations was used to determine the trend of surface water DO, salinity, and temperature over space and time. A 13-year record of two fixed stations was used to determine the temporal nutrient trends. A 10-year record of fixed stations in the southeastern region of Corpus Christi Bay was used to determine the status of disturbance caused by low DO in bottom waters. From 1982 to 2002, there was a significant decrease in surface water DO at a rate of 0.06 mg L⁻¹ yr⁻¹ and a significant increase in surface water temperature at a rate of 0.07°C yr⁻¹. The southeastern region of Corpus Christi Bay had the lowest average DO, and during July and August, DO are steadily declining at a rate of 0.09 mg L⁻¹ yr⁻¹. It is not likely that eutrophication is causing hypoxia, because freshwater inflow rates have significantly decreased since 1941 and nutrient levels have not changed from 1987 to 2000. Even though long-term trends indicate that average surface DO is decreasing, disturbance by hypoxia appears to be stable, but this may be due to just eight years of data. In fact, if the current trend continues, surface water DO will not meet exceptional aquatic life standards (≤5 mgL⁻¹) in 2032.     

Source apportionment in oil spill remediation

A pipe rupture during unloading led to a spillage of 350-700 tonnes of Ca?o Limon, a light sweet crude oil, into San Vicente Bay in 2007. Initial clean-up methods removed the majority of the oil from the sandy beaches although some oil remained on the rocky shores. It was necessary for the responsible party to clean the spilled oil even though at this location there were already crude oil hydrocarbons from previous industrial activity. A biosolvent based on vegetable oil derivatives was used to solubilise the remaining oil and a statistical approach to source apportionment was used to determine the efficacy of the cleaning. Sediment and contaminated rock samples were taken prior to cleaning and again at the same locations two days after application of the biosolvent. The oil was extracted using a modified USEPA Method 3550B. The alkanes were quantified together with oil biomarkers on a GC-MS. The contribution that Ca?o Limon made to the total oil hydrocarbons was calculated from a Partial Least Squares (PLS) analysis using Ca?o Limon crude oil as the source. By the time the biosolvent was applied, there had already been some attenuation of the oil with all alkanes 相似文献   

Measurement of particle concentrations in a dental office

Particles in a dental office can be generated by a number of instruments, such as air-turbine handpieces, low-speed handpieces, ultrasonic scalers, bicarbonate polishers, polishing cups, as well as drilling and air sprays inside the oral cavity. This study examined the generation of particles during dental drilling and measured particle size, mass, and trace elements. The air sampling techniques included both continuous and integrated methods. The following particle continuous measurements were taken every minute: (1) size-selective particle number concentration (Climet); (2) total particle number concentration (PTRAK), and; (3) particle mass concentration (DustTrak). Integrated particle samples were collected for about 5 h on each of five sampling days, using a PM_2.5 sampler (ChemComb) for elemental/organic carbon analysis, and a PM₁₀ sampler (Harvard Impactor) for mass and elemental analyses. There was strong evidence that these procedures result in particle concentrations above background. The dental procedures produced number concentrations of relatively small particles (<0.5 μm) that were much higher than concentrations produced for the relatively larger particles (>0.5 μm). Also, these dental procedures caused significant elevation above background of certain trace elements (measured by X-ray fluorescence) but did not cause any elevation of elemental carbon (measured by thermal optical reflectance). Dental drilling procedures aerosolize saliva and products of drilling, producing particles small enough to penetrate deep into the lungs. The potential health impacts of the exposure of dental personnel to such particles need to be evaluated. Increased ventilation and personal breathing protection could be used to minimize harmful effects.