40 CFR 63.340 - Applicability and designation of sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... National Emission Standards for Chromium Emissions From Hard and Decorative Chromium Electroplating and Chromium Anodizing Tanks § 63.340 Applicability and designation of sources. (a) The affected source to which the provisions of this subpart apply is each chromium electroplating or chromium anodizing tank at...

40 CFR 63.340 - Applicability and designation of sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

... National Emission Standards for Chromium Emissions From Hard and Decorative Chromium Electroplating and Chromium Anodizing Tanks § 63.340 Applicability and designation of sources. (a) The affected source to which the provisions of this subpart apply is each chromium electroplating or chromium anodizing tank at...

Unanticipated potential cancer risk near metal recycling facilities

DOE Office of Scientific and Technical Information (OSTI.GOV)

Raun, Loren, E-mail: raun@rice.edu; Pepple, Karl, E-mail: pepple.karl@epa.gov; Hoyt, Daniel, E-mail: hoyt.daniel@epa.gov

2013-07-15

Metal recycling is an important growing industry. Prior to this study, area sources consisting of metal recycling facilities fell in a category of limited regulatory scrutiny because of assumed low levels of annual emissions. Initiating with community complaints of nuisance from smoke, dust and odor, the Houston Department of Health and Human Services (HDHHS) began a monitoring program outside metal recycler facilities and found metal particulates in outdoor ambient air at levels which could pose a carcinogenic human health risk. In a study of five similar metal recycler facilities which used a torch cutting process, air downwind and outside themore » facility was sampled for eight hours between 6 and 10 times each over 18 months using a mobile laboratory. Ten background locations were also sampled. Iron, manganese, copper, chromium, nickel, lead, cobalt, cadmium and mercury were detected downwind of the metal recyclers at frequencies ranging from 100% of the time for iron to 2% of the time for mercury. Of these metals, chromium, nickel, lead, cobalt, cadmium and mercury were not detected in any sample in the background. Two pairs of samples were analyzed for total chromium and hexavalent chromium to establish a ratio of the fraction of hexavalent chromium in total chromium. This fraction was used to estimate hexavalent chromium at all locations. The carcinogenic risk posed to a residential receptor from metal particulate matter concentrations in the ambient air attributed to the metal recyclers was estimated from each of the five facilities in an effort to rank the importance of this source and inform the need for further investigation. The total risk from these area sources ranged from an increased cancer risk of 1 in 1,000,000 to 6 in 10,000 using the 95th upper confidence limit of the mean of the carcinogenic metal particulate matter concentration, assuming the point of the exposure is the sample location for a residential receptor after accounting for wind direction and the number of shifts that could operate a year. Further study is warranted to better understand the metal air pollution levels in the community and if necessary, to evaluate the feasibility of emission controls and identify operational improvements and best management practices for this industry. This research adds two new aspects to the literature: identification of types and magnitude of metal particulate matter air pollutants associated with a previously unrecognized area source, metal recyclers and their potential risk to health. -- Highlights: • Air monitoring study in response to community complaints found metal contamination. • Metal recyclers found to potentially pose cancer from metal particulates • Chromium, nickel, cobalt and cadmium samples were detected in five metal recyclers. • These metals were not detected in background air samples. • Estimated increased cancer risk ranges from 1 in 1,000,000 to 8 in 10,000.« less

Hydrostratigraphy, soil/sediment chemistry, and water quality, Potomac-Raritan-Magothy aquifer system, Puchack Well Field Superfund site and vicinity, Pennsauken Township, Camden County, New Jersey, 1997-2001

USGS Publications Warehouse

Barringer, Julia L.; Walker, Richard L.; Jacobsen, Eric; Jankowski, Pamela

2010-01-01

Drinking-water supplies from the Potomac-Raritan-Magothy aquifer system at the Puchack well field in Pennsauken Township, Camden County, New Jersey, have been contaminated by hexavalent chromium-the most toxic and mobile form-at concentrations exceeding the New Jersey maximum contaminant level of 100 micrograms per liter. Also, scattered but widespread instances of volatile organic compounds (primarily trichloroethylene) at concentrations that exceed their respective maximum contaminant levels in the area's ground water have been reported. Because inorganic and organic contaminants are present in the ground water underlying the Puchack well field, no water from there has been withdrawn for public supply since 1998, when the U.S. Environmental Protection Agency (USEPA) added the area that contains the Puchack well field to the National Priorities List. As part of the USEPA's investigation of the Puchack Well Field Superfund site, the U.S. Geological Survey (USGS) conducted a study during 1997-2001 to (1) refine previous interpretations of the hydrostratigraphic framework, hydraulic gradients, and local directions of ground-water flow; (2) describe the chemistry of soils and saturated aquifer sediments; and (3) document the quality of ground water in the Potomac-Raritan-Magothy aquifer system in the area. The four major water-bearing units of the Potomac-Raritan-Magothy aquifer system-the Upper aquifer (mostly unsaturated in the study area), the Middle aquifer, the Intermediate Sand (a local but important unit), and the Lower aquifer-are separated by confining units. The confining units contain areas of cut and fill, resulting in permeable zones that permit water to pass through them. Pumping from the Puchack well field during the past 3 decades resulted in downward hydraulic gradients that moved contaminants into the Lower aquifer, in which the production wells are finished, and caused ground water to flow northeast, locally. A comparison of current (1997-2001) water levels near the site of the former pumping center with data from previous investigations indicates that, since pumping at the Puchack well field ceased, the dominant local ground-water flow direction is to the southeast, aligned with regional flow. Chromium concentrations were highest (8,010 micrograms per liter in 2000-01) in water from the Middle aquifer immediately downgradient from a possible source; the extent of this chromium plume is unknown but appears to be small. A second, unrelated, localized chromium plume also was identified in the Middle aquifer. The Intermediate Sand was found to contain an areally extensive plume of chromium-contaminated water, with concentrations up to 6,310 micrograms per liter in 2000-01, and another plume of about the same size, with concentrations up to 4,810 micrograms per liter in 2000-01, was identified in the Lower aquifer. The previous USGS investigation indicated the approximate extent of the combined plumes; the current delineation indicates that their locations have shifted slightly to the southeast since 1998. Concentrations of chromium in ground water decreased at some well locations by as much as 60 percent between sampling rounds in 1997-98 and 1999-2001. The decrease in chromium concentration at a given well could be the result of the chemical reduction of hexavalent chromium and precipitation of the resulting trivalent chromium, the sorption of hexavalent chromium to aquifer materials, or the physical movement of the plumes. Available data indicate that all three processes likely have affected concentrations. The distribution of hexavalent and total chromium in the soils and sediments of a possible source area indicates that some hexavalent chromium has undergone chemical reduction in the soils, but the degree to which this process takes place in the aquifer currently is not known. Nor is it known whether contaminated soils continue to contribute chromium to the aquifer system. Contamination by vola

40 CFR 63.345 - Provisions for new and reconstructed sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

... electroplating, or chromium anodizing); (viii) A description of the air pollution control technique to be used to... National Emission Standards for Chromium Emissions From Hard and Decorative Chromium Electroplating and Chromium Anodizing Tanks § 63.345 Provisions for new and reconstructed sources. (a) This section identifies...

40 CFR 63.345 - Provisions for new and reconstructed sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... electroplating, or chromium anodizing); (viii) A description of the air pollution control technique to be used to... National Emission Standards for Chromium Emissions From Hard and Decorative Chromium Electroplating and Chromium Anodizing Tanks § 63.345 Provisions for new and reconstructed sources. (a) This section identifies...

75 FR 10184 - National Emission Standards for Hazardous Air Pollutants: Area Source Standards for Paints and...

Federal Register 2010, 2011, 2012, 2013, 2014

2010-03-05

... information and technology exchange in various areas of air pollution control. I. Corrections On December 3... CFR Part 63 Environmental protection, Administrative practice and procedure, Air pollution control... section during the grinding and milling of materials containing compounds of cadmium, chromium, lead, or...

Fact Sheet: Final Air Toxics Standards for Area Sources in Seven Industry Sectors

EPA Pesticide Factsheets

This fact sheet discusses national emission standards for acrylic and modacrylic fibers production, carbon black production, chemical manufacturing: chromium compounds, flexible polyurethane foam production and fabrication, lead acid battery manufacturing,

Acrylic and Modacrylic Fibers Production: National Emission Standards for Hazardous Air Pollutants (NESHAP) for Area Sources

EPA Pesticide Factsheets

This NESHAP applies to facilities using pressure or thermal treatment processes involving wood preservatives containing chromium, arsenic, dioxins, or methylene chloride. Page includes rule summary, rule history and additional documents.

Flexible Polyurethane Foam Production and Fabrication: National Emission Standards for Hazardous Air Pollutants (NESHAP) for Area Sources

EPA Pesticide Factsheets

This NESHAP applies to facilities using pressure or thermal treatment processes involving wood preservatives containing chromium, arsenic, dioxins, or methylene chloride. Inlcudes federal register citations, rule history and additional resources.

Dry atmospheric deposition rates of metals along a coastal transect in southern California

NASA Astrophysics Data System (ADS)

Sabin, Lisa D.; Schiff, Kenneth C.

While recent studies indicate atmospheric deposition is a significant source of metals to the Santa Monica Bay and coastal river systems of the Los Angeles area, the spatial extent of the atmospheric source along the entire southern California coast has not been measured in 30 years. This study provides measurements of dry atmospheric deposition of chromium, copper, lead, nickel and zinc at eight sites located along the coast between Santa Barbara and San Diego, and compares these data to historic measurements from the 1970s. Median dry deposition fluxes across sites ranged between 0.23 and 3.6 (chromium), 0.21 and 5.4 (nickel), 0.52 and 14 (lead), 0.89 and 29 (copper), and 4.8 and 160 (zinc) μg m -2 day -1. Differences in metal dry deposition rates observed between sites were dominated by proximity to urban areas and/or other nearby sources, with the highest metal fluxes observed near the Los Angeles Harbor (LAH) and San Diego Bay (SDB) sites. Compared with data from the 1970s, lead fluxes were typically one to two orders of magnitude lower in the present study (2006), indicating atmospheric sources of this metal have decreased over the past three decades in southern California. Chromium fluxes were also lower in 2006 compared with the 1970s, although to a lesser extent than for lead. In contrast, copper and zinc fluxes were typically within the same order of magnitude between the two time periods, with some higher measurements observed in 2006 compared with the 1970s at the LAH and SDB sites. This result indicates atmospheric sources of copper and zinc have not decreased over the past three decades in southern California, and have increased near our harbor/urban sites. Differences in sampling conditions (e.g., Santa Ana winds) and measurement techniques may also explain, in part, the differences observed in metal flux rates for these time periods. However, these limitations were most important for those metals with the smallest difference in flux rates measured in the 1970s vs. 2006 (e.g., chromium).

Risk Assessment Report, Davis Global Communications Site

DTIC Science & Technology

1994-02-23

trivalent chromium . Hexavalent chromium typically is unstable in soil and readily mobilized in both acid and alkaline soils (Bartlett and James, 1979...Environ. Qual. 8: 31. 1 Bartlett, R. J., and J. M. Kimble. 1976a. "Behavior of chromium in soils. I. Trivalent forms." J Environ. QuaL 5: 379-382. 3 i...Background data were not available from these sources for antimony, cadmium, hexavalent chromium , thallium, and silver. Other literature sources, discussed

IN SITU CR(VI) TREATMENT USING A FERROUS IRON-BASED REDUCTANT

EPA Science Inventory

Laboratory and field studies were conducted to evaluate the performance of a ferrous sulfate/ sodium hydrosulfite (dithionite) reductant blend in treating a hexavalent chromium (Cr(VI)) source area and Cr(VI) dissolved phase plume at a former industrial site in Charleston, South ...

Compliance Testing of Phosphoric Acid Anodizing Line Wet Scrubber, Metal Bonding Facility, Building 375, Kelly AFB, Texas

DTIC Science & Technology

1989-06-01

boilers and incinerators). Generally the chromium emissions from the processes are particu- late in nature. The trivalent chromium is converted to...runs at five different boiler and incinerator sources, typically less than 3 percent of the trivalent chromium converts to hexavalent chromium ...Emissions from this process contain 20 to 100 times more trivalent chromium than hexavalent chromium in the sample. In separating the hexavalent chromium

40 CFR 415.176 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... liter Chromium (T) 1.0 0.50 Hexavalent Chromium 0.11 0.060 Nickel (T) 0.80 0.40 In cases where POTWs... an alternate: The limitations for Chromium (T), Hexavalent Chromium, and Nickel (T) are the same as...

40 CFR 415.176 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... liter Chromium (T) 1.0 0.50 Hexavalent Chromium 0.11 0.060 Nickel (T) 0.80 0.40 In cases where POTWs... an alternate: The limitations for Chromium (T), Hexavalent Chromium, and Nickel (T) are the same as...

40 CFR 415.176 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... liter Chromium (T) 1.0 0.50 Hexavalent Chromium 0.11 0.060 Nickel (T) 0.80 0.40 In cases where POTWs... an alternate: The limitations for Chromium (T), Hexavalent Chromium, and Nickel (T) are the same as...

40 CFR 415.176 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... liter Chromium (T) 1.0 0.50 Hexavalent Chromium 0.11 0.060 Nickel (T) 0.80 0.40 In cases where POTWs... an alternate: The limitations for Chromium (T), Hexavalent Chromium, and Nickel (T) are the same as...

40 CFR 63.346 - Recordkeeping requirements.

Code of Federal Regulations, 2014 CFR

2014-07-01

... Standards for Chromium Emissions From Hard and Decorative Chromium Electroplating and Chromium Anodizing... rectifier capacity of hard chromium electroplating tanks at a facility expended during each month of the....342(c)(2); (13) For sources using fume suppressants to comply with the standards, records of the date...

40 CFR 63.346 - Recordkeeping requirements.

Code of Federal Regulations, 2010 CFR

2010-07-01

... Standards for Chromium Emissions From Hard and Decorative Chromium Electroplating and Chromium Anodizing...) Records of the actual cumulative rectifier capacity of hard chromium electroplating tanks at a facility... size in accordance with § 63.342(c)(2); (13) For sources using fume suppressants to comply with the...

40 CFR 63.346 - Recordkeeping requirements.

Code of Federal Regulations, 2013 CFR

2013-07-01

... Standards for Chromium Emissions From Hard and Decorative Chromium Electroplating and Chromium Anodizing... rectifier capacity of hard chromium electroplating tanks at a facility expended during each month of the....342(c)(2); (13) For sources using fume suppressants to comply with the standards, records of the date...

40 CFR 63.346 - Recordkeeping requirements.

Code of Federal Regulations, 2012 CFR

2012-07-01

... Standards for Chromium Emissions From Hard and Decorative Chromium Electroplating and Chromium Anodizing...) Records of the actual cumulative rectifier capacity of hard chromium electroplating tanks at a facility... size in accordance with § 63.342(c)(2); (13) For sources using fume suppressants to comply with the...

40 CFR 63.346 - Recordkeeping requirements.

Code of Federal Regulations, 2011 CFR

2011-07-01

... Standards for Chromium Emissions From Hard and Decorative Chromium Electroplating and Chromium Anodizing...) Records of the actual cumulative rectifier capacity of hard chromium electroplating tanks at a facility... size in accordance with § 63.342(c)(2); (13) For sources using fume suppressants to comply with the...

Heavy metal contamination of sediments in the upper connecting channels of the Great Lakes

USGS Publications Warehouse

Nichols, S. Jerrine; Manny, Bruce A.; Schloesser, Donald W.; Edsall, Thomas A.

1991-01-01

In 1985, sampling at 250 stations throughout the St. Marys, St. Clair, and Detroit rivers and Lake St. Clair — the connecting channels of the upper Great Lakes — revealed widespread metal contamination of the sediments. Concentrations of cadmium, chromium, copper, lead, mercury, nickel, and zinc each exceeded U.S. Environmental Protection Agency sediment pollution guidelines at one or more stations throughout the study area. Sediments were polluted more frequently by copper, nickel, zinc, and lead than by cadmium, chromium, or mercury. Sediments with the highest concentrations of metals were found (in descending order) in the Detroit River, the St. Marys River, the St. Clair River, and Lake St. Clair. Although metal contamination of sediments was most common and sediment concentrations of metals were generally highest near industrial areas, substantial contamination of sediments by metals was present in sediment deposition areas up to 60 km from any known source of pollution.

Investigation of total and hexavalent chromium in filtered and unfiltered groundwater samples at the Tucson International Airport Superfund Site

USGS Publications Warehouse

Tillman, Fred; McCleskey, R. Blaine; Hermosillo, Edyth

2016-01-01

Potential health effects from hexavalent chromium in groundwater have recently become a concern to regulators at the Tucson International Airport Area Superfund site. In 2016, the U.S. Geological Survey sampled 46 wells in the area to characterize the nature and extent of chromium in groundwater, to understand what proportion of total chromium is in the hexavalent state, and to determine if substantial differences are present between filtered and unfiltered chromium concentrations. Results indicate detectable chromium concentrations in all wells, over 75 % of total chromium is in the hexavalent state in a majority of wells, and filtered and unfiltered results differ substantially in only a few high-turbidity total chromium samples.

Investigation of Total and Hexavalent Chromium in Filtered and Unfiltered Groundwater Samples at the Tucson International Airport Superfund Site.

PubMed

Tillman, Fred D; McCleskey, R Blaine; Hermosillo, Edyth

2016-10-01

Potential health effects from hexavalent chromium in groundwater have recently become a concern to regulators at the Tucson International Airport Area Superfund site. In 2016, the U.S. Geological Survey sampled 46 wells in the area to characterize the nature and extent of chromium in groundwater, to understand what proportion of total chromium is in the hexavalent state, and to determine if substantial differences are present between filtered and unfiltered chromium concentrations. Results indicate detectable chromium concentrations in all wells, over 75 % of total chromium is in the hexavalent state in a majority of wells, and filtered and unfiltered results differ substantially in only a few high-turbidity total chromium samples.

Characterization of emission factors related to source activity for trichloroethylene degreasing and chrome plating processes.

PubMed

Wadden, R A; Hawkins, J L; Scheff, P A; Franke, J E

1991-09-01

A study at an automotive parts fabrication plant evaluated four metal surface treatment processes during production conditions. The evaluation provides examples of how to estimate process emission factors from activity and air concentration data. The processes were open tank and enclosed tank degreasing with trichloroethylene (TCE), chromium conversion coating, and chromium electroplating. Area concentrations of TCE and chromium (Cr) were monitored for 1-hr periods at three distances from each process. Source activities at each process were recorded during each sampling interval. Emission rates were determined by applying appropriate mass balance models to the concentration patterns around each source. The emission factors obtained from regression analysis of the emission rate and activity data were 16.9 g TCE/basket of parts for the open-top degreaser; 1.0 g TCE/1000 parts for the enclosed degreaser; 1.48-1.64 mg Cr/1000 parts processed in the hot CrO3/HNO3 tank for the chrome conversion coating; and 5.35-9.17 mg Cr/rack of parts for chrome electroplating. The factors were also used to determine the efficiency of collection for the local exhaust systems serving each process. Although the number of observations were limited, these factors may be useful for providing initial estimates of emissions from similar processes in other settings.

Arsenic, cadmium, lead, and chromium in well water, rice, and human urine in Sri Lanka in relation to chronic kidney disease of unknown etiology.

PubMed

S Herath, H M Ayala; Kawakami, Tomonori; Nagasawa, Shiori; Serikawa, Yuka; Motoyama, Ayuri; Chaminda, G G Tushara; Weragoda, S K; Yatigammana, S K; Amarasooriya, A A G D

2018-04-01

Chronic kidney disease of unknown etiology (CKDu) is spreading gradually in Sri Lanka. In the current research, 1,435 well water samples from all 25 districts of Sri Lanka, 91 rice samples, and 84 human urine samples from both CKDu-endemic and non-endemic areas in Sri Lanka were analyzed for arsenic, cadmium, lead, and chromium to detect whether toxic elements could be a cause of CKDu. The liver-type fatty acid binding protein (L-FABP) concentration and arsenic, cadmium, lead, and chromium concentrations of the urine samples were analyzed to determine the relation of L-FABP with arsenic, cadmium, lead, and chromium. High concentrations of arsenic, cadmium, lead, and chromium were not detected in the well water samples from CKDu-endemic areas. Arsenic, cadmium, and lead contents in the rice samples from both CKDu-endemic and non-endemic areas were well below the Codex standard. There were no relationships between the L-FABP concentration and concentrations of arsenic, cadmium, lead, and chromium in urine. In addition, arsenic, cadmium, lead, and chromium concentrations in human urine samples from CKDu-endemic areas were not significantly different from those from non-endemic areas. These findings indicated that arsenic, cadmium, lead, and chromium could not cause CKDu.

40 CFR 63.11169 - What is the purpose of this subpart?

Code of Federal Regulations, 2011 CFR

2011-07-01

...? 63.11169 Section 63.11169 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Surface Coating Operations at Area Sources What This Subpart Covers § 63.11169 What is the purpose of this... containing compounds of chromium (Cr), lead (Pb), manganese (Mn), nickel (Ni), or cadmium (Cd), collectively...

40 CFR 63.11169 - What is the purpose of this subpart?

Code of Federal Regulations, 2012 CFR

2012-07-01

...? 63.11169 Section 63.11169 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Surface Coating Operations at Area Sources What This Subpart Covers § 63.11169 What is the purpose of this... containing compounds of chromium (Cr), lead (Pb), manganese (Mn), nickel (Ni), or cadmium (Cd), collectively...

40 CFR 63.11169 - What is the purpose of this subpart?

Code of Federal Regulations, 2014 CFR

2014-07-01

...? 63.11169 Section 63.11169 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Surface Coating Operations at Area Sources What This Subpart Covers § 63.11169 What is the purpose of this... containing compounds of chromium (Cr), lead (Pb), manganese (Mn), nickel (Ni), or cadmium (Cd), collectively...

40 CFR 63.11169 - What is the purpose of this subpart?

Code of Federal Regulations, 2013 CFR

2013-07-01

...? 63.11169 Section 63.11169 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Surface Coating Operations at Area Sources What This Subpart Covers § 63.11169 What is the purpose of this... containing compounds of chromium (Cr), lead (Pb), manganese (Mn), nickel (Ni), or cadmium (Cd), collectively...

40 CFR 63.11169 - What is the purpose of this subpart?

Code of Federal Regulations, 2010 CFR

2010-07-01

...? 63.11169 Section 63.11169 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Surface Coating Operations at Area Sources What This Subpart Covers § 63.11169 What is the purpose of this... containing compounds of chromium (Cr), lead (Pb), manganese (Mn), nickel (Ni), or cadmium (Cd), collectively...

Predictors of serum chromium levels after stainless steel posterior spinal instrumentation for adolescent idiopathic scoliosis.

PubMed

Rackham, Matthew D; Cundy, Thomas P; Antoniou, Georgia; Freeman, Brian J C; Sutherland, Leanne M; Cundy, Peter J

2010-04-20

Prospective cohort study. To determine the predictors of serum chromium levels after stainless steel posterior spinal instrumentation for adolescent idiopathic scoliosis. Abnormally elevated serum chromium levels have been detected in patients with adolescent idiopathic scoliosis after stainless steel instrumentation. To date, the relationship among serum chromium levels, time of implantation, and implant characteristics (including surface area, rod length, numbers of hooks, screws, and cross connectors) has not been studied. Thirty patients with adolescent idiopathic scoliosis undergoing posterior instrumented spinal arthrodesis using stainless steel implants between 1998 and 2002 were prospectively studied. Serum chromium levels were measured between October 2006 and June 2007. Postoperative radiographs were used to measure rod lengths, number of hooks, screws, cross-connectors, and cables. The surface area of each component and the total surface area for each patient were calculated. Possible associations between serum chromium levels, time of implantation, and implant characteristics were investigated. Implant exposure, whether expressed in the form of total metal implant surface area, rod length, or number of metal interfaces, was found to be positively associated with serum chromium levels. Specifically, chromium levels increased by a multiplicative factor of 1.0060 for every additional square centimeter of total metal implant surface area (P = 0.02). In addition, the chromium level was found to decrease by a multiplicative factor of 0.7766 for every additional year since surgery (P = 0.02). After adjusting for the number of years since surgery, metal implant exposure is positively associated with elevated serum chromium levels in adolescent idiopathic scoliosis patients with stainless steel posterior spinal implants. This is the first study to identify statistically significant positive associations between specific spinal implant characteristics (other than corrosion identified by radiographs) and serum chromium levels.

AQUIFER TESTING AND REBOUND STUDY IN SUPPORT OF THE 100-H DEEP CHROMIUM INVESTIGATION

DOE Office of Scientific and Technical Information (OSTI.GOV)

SMOOT JL

2010-11-05

The 100-HR-3 Groundwater Operable Unit (OU) second Comprehensive Environmental Response, Compensation, and Liability Act of 1980 (CERCLA) 5-year review (DOEIRL-2006-20, The Second CERCLA Five-Year Review Report for the Hanford Site) set a milestone to conduct an investigation of deep hexavalent chromium contamination in the sediments of the Ringold upper mud (RUM) unit, which underlies the unconfined aquifer in the 100-H Area. The 5-year review noted that groundwater samples from one deep well extending below the aquitard (i.e., RUM) exceeded both the groundwater standard of 48 parts per billion (ppb) (Ecology Publication 94-06, Model Toxics Control Act Cleanup Statute and Regulation)more » and the federal drinking water standard of 100 {mu}g/L for hexavalent chromium. The extent of hexavalent chromium contamination in this zone is not well understood. Action 12-1 from the 5-year review is to perform additional characterization of the aquifer below the initial aquitard. Field characterization and aquifer testing were performed in the Hanford Site's 100-H Area to address this milestone. The aquifer tests were conducted to gather data to answer several fundamental questions regarding the presence of the hexavalent chromium in the deep sediments of the RUM and to determine the extent and magnitude of deeper contamination. The pumping tests were performed in accordance with the Description of Work for Aquifer Testing in Support of the 100-H Deep Chromium Investigation (SGW-41302). The specific objectives for the series of tests were as follows: (1) Evaluate the sustainable production of the subject wells using step-drawdown and constant-rate pumping tests. (2) Collect water-level data to evaluate the degree of hydraulic connection between the RUM and the unconfined (upper) aquifer (natural or induced along the well casing). (3) Evaluate the hydraulic properties of a confined permeable layer within the RUM.; (4) Collect time-series groundwater samples during testing to evaluate the extent and persistence of hexavalent chromium in the deeper zones. Use data collected to refine the current conceptual model for the 100-H Area unconfined aquifer and the RUM in this area. (5) Evaluate the concentration 'rebound' in the unconfined aquifer of hexavalent chromium and the contaminants of concern during shutdown of the extraction wells. Measure co-contaminants at the beginning, middle, and end of each pumping test. The RUM is generally considered an aquitard in the 100-HR-3 OU; however, several water-bearing sand layers are present that are confined within the RUM. The current hydrogeologic model for the 100-H Area aquifer system portrays the RUM as an aquitard layer that underlies the unconfined aquifer, which may contain permeable zones, stringers, or layers. These permeable zones may provide pathways for chromium to migrate deeper into the RUM under certain hydrogeologic conditions. One condition may be the discharge of large volumes of cooling water that occurred near the former H Reactor, which caused a mound of groundwater to form 4.9 to 10.1 m (16 to 33 ft) above the natural water table. The cooling water reportedly contained 1 to 2 mglL of hexavalent chromium for corrosion prevention. Three alternate hypotheses for the introduction of hexavalent chromium into the RUM are as follows: (1) Local groundwater with higher concentrations of hexavalent chromium originating from reactor operations at H Reactor was driven by high heads from groundwater mounding in the unconfined aquifer into the RUM via permeable pathways in the upper surface of the RUM. (2) Local groundwater with hexavalent chromium was introduced from the unconfined aquifer via well boreholes, either during drilling or as a result of poor well construction, allowing hydraulic communication between the unconfined aquifer and the RUM. (3) Hexavalent chromium migrated across the Hom area within the more permeable zones of the RUM. The three wells used for the aquifer pumping tests (199-H3-2C, 199-H4-12C, and 199-H4-15CS) exhibit hexavalent chromium contamination in confined aquifer groundwater that may be the result of one of the mechanisms described above. The purpose of the aquifer testing was to gather data to help refine the conceptual model for the source of deep contamination, examine the potential hydraulic connection between the RUM and the unconfined aquifer, evaluate the hydraulic properties of a confined layer within the RUM, and indicate the extent of hexavalent chromium contamination in the RUM. The results of this study, in conjunction with the recent Hom area investigation (DOE/RL-2008-42, Hydrogeological Summary Report for 600 Area Between 100-D and 100-H for the 100-HR-3 Groundwater Operable Unit), suggest that the first hypothesis is the most reasonable explanation. The results indicate persistent chromium concentrations over the duration of the tests, suggesting a large-scale emplacement of chromium.« less

Assessment of atmospheric metal pollution in the urban area of Mexico City, using Ficus benjamina as biomonitor.

PubMed

Guzmán-Morales, Janin; Morton-Bermea, Ofelia; Hernández-Álvarez, Elizabeth; Rodríguez-Salazar, María Teresa; García-Arreola, María Elena; Tapia-Cruz, Víctor

2011-05-01

Concentrations of vanadium, chromium, cobalt, nickel, copper, zinc, antimony, and lead were measured in Ficus benjamina leaves from the Mexico City urban area in order to assess their enrichment against background values. The instrumental analysis was performed using inductively coupled plasma mass spectrometry and the analytical method was tested using two certified reference materials from the National Institute of Standards and Technology (1547 Peach Leaves and 1573a Tomato Leaves). Enrichment factors were calculated, i.e., total to background concentration ratio, for each metal. Low enrichments of vanadium, cobalt, nickel, and copper (≈2), and mild enrichments of chromium and zinc (4.4, 4.5 respectively) were found in the entire area; oppositely, high enrichments were assessed for antimony (28.6) and lead (17.2). However, results indicate that metal concentrations strongly depend on the specific urban sub-area. Increments of metals were attributed to natural, vehicular, and industrial sources. © Springer Science+Business Media, LLC 2011

40 CFR Table 1 to Subpart Nnnnnn... - HAP Emissions Sources

Code of Federal Regulations, 2013 CFR

2013-07-01

... roasting kiln. g. Quench tanks. 5. Chromium hydrate production a. Furnace used to produce chromium hydrate. b. Chromium hydrate grinding unit. As required in § 63.11411(a), you must comply with the...

40 CFR Table 1 to Subpart Nnnnnn... - HAP Emissions Sources

Code of Federal Regulations, 2010 CFR

2010-07-01

... roasting kiln. g. Quench tanks. 5. Chromium hydrate production a. Furnace used to produce chromium hydrate. b. Chromium hydrate grinding unit. As required in § 63.11411(a), you must comply with the...

40 CFR Table 1 to Subpart Nnnnnn... - HAP Emissions Sources

Code of Federal Regulations, 2012 CFR

2012-07-01

... roasting kiln. g. Quench tanks. 5. Chromium hydrate production a. Furnace used to produce chromium hydrate. b. Chromium hydrate grinding unit. As required in § 63.11411(a), you must comply with the...

40 CFR Table 1 to Subpart Nnnnnn... - HAP Emissions Sources

Code of Federal Regulations, 2014 CFR

2014-07-01

... roasting kiln. g. Quench tanks. 5. Chromium hydrate production a. Furnace used to produce chromium hydrate. b. Chromium hydrate grinding unit. As required in § 63.11411(a), you must comply with the...

40 CFR Table 1 to Subpart Nnnnnn... - HAP Emissions Sources

Code of Federal Regulations, 2011 CFR

2011-07-01

... roasting kiln. g. Quench tanks. 5. Chromium hydrate production a. Furnace used to produce chromium hydrate. b. Chromium hydrate grinding unit. As required in § 63.11411(a), you must comply with the...

40 CFR 424.25 - Standards of performance for new sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 0.016 Chromium total .001 .0005 Chromium VI .0001 .00005 Manganese total .011 .005 Cyanide total .0005 .0003 Phenols .0004 .0002 pH (1) (1) English units (lb/Mwh) TSS .071 .035 Chromium total .002 .0012 Chromium VI .0002 .0001 Manganese total .023 .012 Cyanide total .001 .0006 Phenols .0009 .0005 pH...

40 CFR 424.25 - Standards of performance for new sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 0.016 Chromium total .001 .0005 Chromium VI .0001 .00005 Manganese total .011 .005 Cyanide total .0005 .0003 Phenols .0004 .0002 pH (1) (1) English units (lb/Mwh) TSS .071 .035 Chromium total .002 .0012 Chromium VI .0002 .0001 Manganese total .023 .012 Cyanide total .001 .0006 Phenols .0009 .0005 pH...

40 CFR 424.25 - Standards of performance for new sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 0.016 Chromium total .001 .0005 Chromium VI .0001 .00005 Manganese total .011 .005 Cyanide total .0005 .0003 Phenols .0004 .0002 pH (1) (1) English units (lb/Mwh) TSS .071 .035 Chromium total .002 .0012 Chromium VI .0002 .0001 Manganese total .023 .012 Cyanide total .001 .0006 Phenols .0009 .0005 pH...

SITE CHARACTERIZATION OF A CHROMIUM SOURCE AREA AT THE USGS SUPPORT CENTER, ELIZABETH CITY, NC

EPA Science Inventory

Chromic and sulfuric acid wastes had discharged through a hole in the concrete floor of a chrome-plating shop located within a hangar at the U.S. Coast Guard Support Center near Elizabeth City, North Carolina and infiltrated the soils and groundwater beneath the shop. Following i...

Reconnaissance of water-quality characteristics of streams in the City of Charlotte and Mecklenburg County, North Carolina

USGS Publications Warehouse

Eddins, W.H.; Crawford, J.K.

1984-01-01

In 1979-81, water samples were collected from 119 sites on streams throughout the City of Charlotte and Mecklenburg County, North Carolina, and were analyzed for specific conductance, dissolved chloride, hardness, pH, total alkalinity, total phosphorus, trace elements, arsenic, cadmium, chromium, copper, iron, lead, manganese, mercury, silver, and zinc and biological measures including dissolved oxygen, biochemical oxygen demand, fecal coliform bacteria, and fecal streptococcus bacteria. Sampling was conducted during both low flow (base flow) and high flow. Several water-quality measures including pH, total arsenic, total cadmium, total chromium, total copper, total iron, total lead, total manganese, total mercury, total silver, total zinc, dissolved oxygen, and fecal coliform bacteria at times exceeded North Carolina water-quality standards in various streams. Runoff from non-point sources appears to contribute more to the deterioration of streams in Charlotte and Mecklenburg County than point-source effluents. Urban and industrial areas contribute various trace elements. Residential and rural areas and municipal waste-water treatment plants contribute high amounts of phosphorus.

40 CFR 424.15 - Standards of performance for new sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

... values for 30 consecutive days shall not exceed— Metric units (kg/Mwh) TSS 0.024 0.012 Chromium total .0008 .0004 Chromium VI .00008 .00004 Manganese total .008 .0039 pH (1) (1) English units (lb/Mwh) TSS .052 .026 Chromium total .0017 .0009 Chromium VI .0002 .0001 Manganese total .017 .0086 pH (1) (1) 1...

40 CFR 424.15 - Standards of performance for new sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

... values for 30 consecutive days shall not exceed— Metric units (kg/Mwh) TSS 0.024 0.012 Chromium total .0008 .0004 Chromium VI .00008 .00004 Manganese total .008 .0039 pH (1) (1) English units (lb/Mwh) TSS .052 .026 Chromium total .0017 .0009 Chromium VI .0002 .0001 Manganese total .017 .0086 pH (1) (1) 1...

40 CFR 424.15 - Standards of performance for new sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

... values for 30 consecutive days shall not exceed— Metric units (kg/Mwh) TSS 0.024 0.012 Chromium total .0008 .0004 Chromium VI .00008 .00004 Manganese total .008 .0039 pH (1) (1) English units (lb/Mwh) TSS .052 .026 Chromium total .0017 .0009 Chromium VI .0002 .0001 Manganese total .017 .0086 pH (1) (1) 1...

RESULTS FROM RECENT SCIENCE AND TECHNOLOGY INVESTIGATIONS TARGETING CHROMIUM IN THE 100D AREA HANFORD SITE WASHINGTON USA

DOE Office of Scientific and Technical Information (OSTI.GOV)

PETERSEN SW; THOMPSON KM; TONKIN MJ

2009-12-03

Sodium dichromate was used in Hanford's 100D Area during the reactor operations period of 1950 to 1964 to retard corrosion in the reactor cooling systems. Some of the sodium dichromate was released to the environment by spills and/or leaks from pipelines used to deliver the chemical to water treatment plants in the area. As a result, hexavalent chromium [Cr(VI)] has migrated through the vadose zone to the groundwater and contaminated nearly 1 km{sup 2} of groundwater to above the drinking water standard of 48 {micro}g/L. Three technology tests have recently been completed in this area to characterize the source areamore » of the plumes and evaluate alternative methods to remove Cr(VI) from groundwater. These are (1) refine the source area of the southern plume; (2) test electrocoagulation as an alternative groundwater treatment technology; and (3) test the ability to repair a permeable reactive barrier by injecting micron or nanometer-size zero-valent iron (ZVI). The projects were funded by the US Department of Energy as part of a program to interject new technologies and accelerate active cleanup. Groundwater monitoring over the past 10 years has shown that Cr(VI) concentrations in the southern plume have not significantly diminished, strongly indicating a continuing source. Eleven groundwater wells were installed in 2007 and 2008 near a suspected source area and monitored for Cr(VI) and groundwater levels. Interpretation of these data has led to refinement of the source area location to an area of less than 1 hectare (ha, 2.5 acres). Vadose zone soil samples collected during drilling did not discover significant concentrations of Cr(VI), indicating the source is localized, with a narrow wetted path from the surface to the water table. Electrocoagulation was evaluated through a pilot-scale treatability test. Over 8 million liters of groundwater were treated to Cr(VI) concentrations of {le}20 {micro}g/L. The test determined that this technology has the potential to treat Cr(VI) to these low levels, but system reliability and operational complexity rendered electrocoagulation less cost effective than the baseline technology of ion exchange. Laboratory and field tests were conducted to evaluate the practicality of injecting ZVI into the aquifer to increase the lifespan and effectiveness of an existing permeable reactive barrier. From a database of 30 ZVI materials, 6 were chosen and tested in the laboratory to determine their geochemical and physical performance under simulated 100D aquifer conditions. The best-performing ZVI was injected into the aquifer and met the primary goals of communicating the iron at least 7 meters from the injection point and reducing the aquifer to transform mobile Cr(VI) to trivalent chromium Cr(III), which is effectively immobile in the aquifer.« less

Hollow tin/chromium whiskers

NASA Astrophysics Data System (ADS)

Cheng, Jing; Vianco, Paul T.; Li, James C. M.

2010-05-01

Tin whiskers have been an engineering challenge for over five decades. The mechanism has not been agreed upon thus far. This experiment aimed to identify a mechanism by applying compressive stresses to a tin film evaporated on silicon substrate with an adhesion layer of chromium in between. A phenomenon was observed in which hollow whiskers grew inside depleted areas. Using focused ion beam, the hollow whiskers were found to contain both tin and chromium. At the bottom of the depleted areas, thin tin/tin oxide film remained over the chromium layer. It indicates that tin transport occurred along the interface between tin and chromium layers.

40 CFR 421.305 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... off-gas wet air pollution control. PSES for the Primary and Secondary Titanium Subcategory Pollutant... pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496 0.215 (b) Chlorination Area-vent wet air pollution control. PSES for the Primary and Secondary...

40 CFR 421.304 - Standards of performance for new sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

... air pollution control. NSPS Limitations for the Primary and Secondary Titanium Subcategory Pollutant... pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496... of 7.5 to 10.0 at all times. (b) Chlorination area-vent wet air pollution control. NSPS Limitations...

40 CFR 421.304 - Standards of performance for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... air pollution control. NSPS Limitations for the Primary and Secondary Titanium Subcategory Pollutant... pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496... of 7.5 to 10.0 at all times. (b) Chlorination area-vent wet air pollution control. NSPS Limitations...

40 CFR 421.305 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

... off-gas wet air pollution control. PSES for the Primary and Secondary Titanium Subcategory Pollutant... pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496 0.215 (b) Chlorination Area-vent wet air pollution control. PSES for the Primary and Secondary...

Chromium: a review of environmental and occupational toxicology.

PubMed

Bencko, V

1985-01-01

The following topics are covered in this brief review on the environmental and occupational toxicology of chromium: occurrence, production and uses of chromium and chromium compounds; experimental toxicology; chromium toxicity for man; hygienic and ecologic aspects of chromium contamination of the environment. The review provides a conclusive evidence which suggests that chromium, especially its hexavalent form, is both toxic and carcinogenic, but its trivalent form is physiologically essential in the metabolism of insulin. It is also emphasized that among the major sources of environmental chromium today are the cement industry and the increasingly widespread use of chromium compounds added as an anticorrosion admixture to a variety of cooling systems, e.g. in large power plants, which may greatly contribute to the overall pollution of outdoor air at the sites.

40 CFR 63.11432 - What General Provisions apply to this subpart?

Code of Federal Regulations, 2010 CFR

2010-07-01

... chromium, arsenic, dioxins, or methylene chloride, you must comply with the requirements of the General... new or existing affected source that uses any wood preservative containing chromium, arsenic, dioxins... uses any wood preservative containing chromium, arsenic, dioxins, or methylene chloride, you must...

40 CFR 63.11432 - What General Provisions apply to this subpart?

Code of Federal Regulations, 2011 CFR

2011-07-01

... chromium, arsenic, dioxins, or methylene chloride, you must comply with the requirements of the General... new or existing affected source that uses any wood preservative containing chromium, arsenic, dioxins... uses any wood preservative containing chromium, arsenic, dioxins, or methylene chloride, you must...

Hierarchical structures of carbon nanotubes and arrays of chromium-capped silicon nanopillars: formation and electrical properties.

PubMed

Koch, Stefan; Joshi, Ravi K; Noyong, Michael; Timper, Jan; Schneider, Jörg J; Simon, Ulrich

2012-09-10

The formation of stochastically oriented carbon-nanotube networks on top of an array of free-standing chromium-capped silicon nanopillars is reported. The combination of nanosphere lithography and chemical vapor deposition enables the construction of nanostructures that exhibit a hierarchical sequence of structural sizes. Metallic chromium serves as an etching mask for Si-pillar formation and as a nucleation site for the formation of carbon nanotubes through the chemical vapor deposition of ethene, ethanol, and methane, respectively, thereby bridging individual pillars from top to top. Iron and cobalt were applied onto the chromium caps as catalysts for CNT growth and the influence of different carbon sources and different gas-flow rates were investigated. The carbon nanotubes were structurally characterized and their DC electrical properties were studied by in situ local- and ex situ macroscopic measurements, both of which reveal their semiconductor properties. This process demonstrates how carbon nanotubes can be integrated into Si-based semiconductors and, thus, this process may be used to form high-surface-area sensors or new porous catalyst supports with enhanced gas-permeation properties. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Navy Electroplating Pollution Control Technology Assessment Manual.

DTIC Science & Technology

1984-02-01

quality. Dummying of chromium baths is used in the special case where high cathode-to-anode 5ea ratio has resulted in build up of trivalent chromium (Cr...Dummying with a high anode -to-cat hode area ratio can be 6used to reoxidize the trivalent to hexavalent chromium (Cr ).Proper scheduling of work can...unit processes: * Chromium reduction (if needed) of segregated chromium waste streams to reduce the chromium from its hexavalent form to the trivalent

40 CFR 420.126 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... Zinc 0.000376 0.000125 Chromium (hexavalent) 1 0.0000376 0.0000125 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge wastewaters from the chromate... 0.00150 0.000500 Chromium (hexavalent) 1 0.000150 0.0000501 1 The limitations for hexavalent...

40 CFR 420.126 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... Zinc 0.000376 0.000125 Chromium (hexavalent) 1 0.0000376 0.0000125 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge wastewaters from the chromate... 0.00150 0.000500 Chromium (hexavalent) 1 0.000150 0.0000501 1 The limitations for hexavalent...

40 CFR 420.126 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... Zinc 0.000376 0.000125 Chromium (hexavalent) 1 0.0000376 0.0000125 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge wastewaters from the chromate... 0.00150 0.000500 Chromium (hexavalent) 1 0.000150 0.0000501 1 The limitations for hexavalent...

40 CFR 420.126 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... Zinc 0.000376 0.000125 Chromium (hexavalent) 1 0.0000376 0.0000125 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge wastewaters from the chromate... 0.00150 0.000500 Chromium (hexavalent) 1 0.000150 0.0000501 1 The limitations for hexavalent...

Ductile-brittle transition of thoriated chromium.

NASA Technical Reports Server (NTRS)

Wilcox, B. A.; Veigel, N. D.; Clauer, A. H.

1972-01-01

Unalloyed chromium and chromium containing approximately 3 wt % ThO2 were prepared from powder produced by a chemical vapor deposition process. When rolled to sheet and tested in tension, it was found that the thoriated material had a lower ductile-to-brittle transition temperature (DBTT) than unalloyed chromium. This ductilizing was evident both in the as-rolled condition and after the materials had been annealed for 1 hour at 1200 C. The improved ductility in thoriated chromium may be associated with several possible mechanisms: (1) particles may disperse slip, such that critical stress or strain concentrations for crack nucleation are more difficult to achieve; (2) particles may act as dislocation sources, thus providing mobile dislocations in this normally source-poor material, in a manner similar to prestraining; and (3) particles in grain boundaries may help to transmit slip across the boundaries, thus relieving stress concentrations and inhibiting crack nucleation.

Environmental exposure to arsenic and chromium in an industrial area.

PubMed

Vimercati, Luigi; Gatti, Maria F; Gagliardi, Tommaso; Cuccaro, Francesco; De Maria, Luigi; Caputi, Antonio; Quarato, Marco; Baldassarre, Antonio

2017-04-01

Arsenic and chromium are widespread environmental contaminants that affect global health due to their toxicity and carcinogenicity. To date, few studies have investigated exposure to arsenic and chromium in a population residing in a high-risk environmental area. The aim of this study is to evaluate the exposure to arsenic and chromium in the general population with no occupational exposure to these metals, resident in the industrial area of Taranto, Southern Italy, through biological monitoring techniques. We measured the levels of chromium, inorganic arsenic, and methylated metabolites, in the urine samples of 279 subjects residing in Taranto and neighboring areas. Qualified health staff administered a standardized structured questionnaire investigating lifestyle habits and controlling for confounding factors. The biological monitoring data showed high urinary concentrations of both the heavy metals investigated, particularly Cr. On this basis, it will be necessary to carry out an organized environmental monitoring program, taking into consideration all exposure routes so as to correlate the environmental concentrations of these metals with the biomonitoring results.

40 CFR 421.306 - Pretreatment standards for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... exceed the following values: (a) Chlorination off-gas wet air pollution control. PSNS for the Primary and... average mg/kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496 0.215 (b) Chlorination area-vent wet air pollution control. PSNS for...

40 CFR 421.306 - Pretreatment standards for new sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

... exceed the following values: (a) Chlorination off-gas wet air pollution control. PSNS for the Primary and... average mg/kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496 0.215 (b) Chlorination area-vent wet air pollution control. PSNS for...

40 CFR 424.25 - Standards of performance for new sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

... and Other Smelting Operations With Wet Air Pollution Control Devices Subcategory § 424.25 Standards of... 0.016 Chromium total .001 .0005 Chromium VI .0001 .00005 Manganese total .011 .005 Cyanide total .0005 .0003 Phenols .0004 .0002 pH (1) (1) English units (lb/Mwh) TSS .071 .035 Chromium total .002...

40 CFR 424.25 - Standards of performance for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... and Other Smelting Operations With Wet Air Pollution Control Devices Subcategory § 424.25 Standards of... 0.016 Chromium total .001 .0005 Chromium VI .0001 .00005 Manganese total .011 .005 Cyanide total .0005 .0003 Phenols .0004 .0002 pH (1) (1) English units (lb/Mwh) TSS .071 .035 Chromium total .002...

40 CFR 420.125 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2011 CFR

2011-07-01

... product Lead 0.00113 0.000376 Zinc 0.00150 0.000500 Chromium (hexavalent) 1 0.000150 0.0000501 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge... product Lead 0.00451 0.00150 Zinc 0.00601 0.00200 Chromium (hexavalent) 1 0.000601 0.000200 1 The...

40 CFR 420.125 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2014 CFR

2014-07-01

... product Lead 0.00113 0.000376 Zinc 0.00150 0.000500 Chromium (hexavalent) 1 0.000150 0.0000501 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge... product Lead 0.00451 0.00150 Zinc 0.00601 0.00200 Chromium (hexavalent) 1 0.000601 0.000200 1 The...

40 CFR 420.125 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2012 CFR

2012-07-01

... product Lead 0.00113 0.000376 Zinc 0.00150 0.000500 Chromium (hexavalent) 1 0.000150 0.0000501 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge... product Lead 0.00451 0.00150 Zinc 0.00601 0.00200 Chromium (hexavalent) 1 0.000601 0.000200 1 The...

40 CFR 420.125 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2013 CFR

2013-07-01

... product Lead 0.00113 0.000376 Zinc 0.00150 0.000500 Chromium (hexavalent) 1 0.000150 0.0000501 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge... product Lead 0.00451 0.00150 Zinc 0.00601 0.00200 Chromium (hexavalent) 1 0.000601 0.000200 1 The...

Hexavalent chromium emissions from aerospace operations: A case study

DOE Office of Scientific and Technical Information (OSTI.GOV)

Chaurushia, A.; Bajza, C.

1994-12-31

Northrop Aircraft Division (NAD) is subject to several air toxic regulations such as EPA SARA Title 3, California Assembly Bill 2588 (AB2588), and Proposition 65 and is a voluntary participant in air toxic emissions reduction programs such as the EPA 33/50 and MERIT Program. To quantify emissions, NAD initially followed regulatory guidelines which recommend that emission inventories of air toxics be based on engineering assumptions and conservative emission factors in absence of specific source test data. NAD was concerned that Chromium VI emissions from NAD`s spray coating and chemical tank line operations were not representative due to these techniques. Moremore » recently, NAD has relied upon information from its ongoing source testing program to determine emission rates of Chromium VI. Based on these source test results, NAD revised emission calculations for use in Chromium VI inventories, impact assessments and control strategies. NAD has been successful in demonstrating a significant difference between emissions calculated utilizing the source test results and emissions based on the traditional mass balance using agency suggested methods.« less

Acute toxicity by water containing hexavalent or trivalent chromium in native Brazilian fish, Piaractus mesopotamicus: anatomopathological alterations and mortality.

PubMed

Castro, Marcello Pardi; de Moraes, Flávio Ruas; Fujimoto, Rodrigo Yudi; da Cruz, Claudinei; Belo, Marco Antonio de Andrade; de Moraes, Julieta Rodini Engrácia

2014-02-01

This study evaluated the toxicity of hexavalent and trivalent compounds of chromium to the pacu, Piaractus mesopotamicus, in acute exposures of 96 h through mortality and histopathological responses. Hexavalent potassium dichromate was more toxic than trivalent compounds of chromium chloride, chromium oxide and chromium carbochelate. Sufficient mortalities occurred only with potassium dichromate to yield an LC50 value at 124.2 mg L(-1). Hexavalent chromium caused reversible and irreversible lesions, which may affect organ functionality. Histopathological evaluation showed that trivalent chromium caused lesions of lower severity. Pacu subjected to different concentrations of chromium carbochelate showed no histopathological changes in the kidneys, liver, skin and gills, being similar to those of the control fish. Among the three sources of Cr(3+), only chromium chloride at 200 mg L(-1) resulted in mortality, which reached 100 % within the first 18 h. These findings confirm that trivalent chromium, when administered within recommended levels, may be used safely in aquaculture.

Sources, transport and alterations of metal compounds: an overview. I. Arsenic, beryllium, cadmium, chromium, and nickel.

PubMed Central

Fishbein, L

1981-01-01

An overview is presented of the current state of knowledge of the salient aspects of the sources, transport, and alterations of arsenic, beryllium, cadmium, chromium, and nickel. This information is considered vital for a better assessment of the scope of potential human hazard to these ubiquitous toxicants and their compounds. Stress is focused on both natural and industrial activities, particularly on the latter's projected trends. Increasing use patterns per se of most of these metals, as well as aspects of waste disposal and the anticipated increased combustion of fossil fuels for power generation and space heating (particularly in the United States), are major causes of potential health concern. Additionally, attention is drawn to the need for increased research to fill the gaps in our knowledge in these vital areas, all in the hope of permitting a more facile identification and quantification of the potential hazard to exposure to these agents. PMID:7023934

Genesis and transport of hexavalent chromium in the system ophiolitic rocks - groundwater

NASA Astrophysics Data System (ADS)

Shchegolikhina, Anastasia; Guadagnini, Laura; Guadagnini, Alberto

2015-04-01

Our study aims at contributing to the quantification and characterization of chromium transport processes from host rocks and soil matrices to groundwater. We focus on dissolved hexavalent chromium detected in groundwaters of geological regions with ophiolitic rocks (ophiolites and serpentinites) inclusions due to its critical ecological impact. (Oze et al., 2004). Despite the large number of analyses on the occurrence of high concentrations of hazardous hexavalent chromium ions in natural waters, only few studies were performed with the objective of identifying and investigating the geochemical reactions which could occur in the natural system rock - groundwater - dissolved chromium (Fantoni et al., 2002, Stephen and James, 2004, Lelli et al., 2013). In this context, there is a need for integration of results obtained from diverse studies in various regions and settings to improve our knowledge repository. Our theoretical analyses are grounded and driven by practical scenarios detected in subsurface reservoirs exploited for civil and industrial use located in the Emilia-Romagna region (Italy). Available experimental datasets are complemented with data from other international regional-scale settings (Altay mountains region, Russia). Modeling of chromium transformation and migration particularly includes characterization of the multispecies geochemical system. A key aspect of our study is the analysis of the complex competitive sorption processes governing heavy metal evolution in groundwater. The results of the research allow assessing the critical qualitative features of the mechanisms of hexavalent chromium ion mobilization from host rocks and soils and the ensuing transformation and migration to groundwater under the influence of diverse environmental factors. The study is then complemented by the quantification of the main sources of uncertainty associated with prediction of heavy metal contamination levels in the groundwater system explored. Fantoni, D., Brozzo, G., Canepa, M., Cipolli, F., Marini, L., Ottonello, G., Zuccolini, M., 2002. Natural hexavalent chromium in groundwaters interacting with ophiolitic rocks. Environmental Geology 42, 871-882. Lelli, M., Grassi, S., Amadori, M., Franceschini, F., 2013. Natural Cr(VI) contamination of groundwater in the Cecina coastal area and its inner sectors (Tuscany, Italy). Environmental Earth Sciences 71, 3907-3919. Oze, C., Fendorf, S., Bird, D.K., Coleman, R.G., 2004. Chromium geochemistry of serpentine soils. International Geology Review 46, 97-126. Stephen, M.T., James, A.J., 2004. Overview of chromium (VI) in the environment. Chromium (VI) Handbook. CRC Press, pp. 21.

[Research on the application of in-situ biological stabilization solidification technology in chromium contaminated site management].

PubMed

Zhang, Jian-rong; Li, Juan; Xu, Wei

2013-09-01

In-situ biological stabilization solidification (SS) technology is an effective ground water risk control method for chromium contaminated sites. Through on-site engineering test, this paper has preliminarily validated the remediation effect of in-situ SS method on a southern chromium contaminated site. The engineering test site has an area of approximately 600 m2, and is located at the upstream of the contaminated area. Due to the severe contamination of chromium, the total chromium concentration reached up to 11,850 mg x kg(-1), while the hexavalent chromium concentration reached up to 349 mg x kg(-1), and the most severely contaminated soil had a depth of -0.5 - -2 m. Variations in hexavalent chromium and total chromium concentration in groundwater were observed through the injection of reducing agents and microbial regulators into the injection wells in the test site, and through the monitoring analysis at different time and different depth under the action of the injection agents. Results of the engineering test showed that the on-site SS technology significantly changed the chromium speciation in soil and then reduced the migration of chromium, thus the groundwater risk was reduced. The injected agents had a good effect of hexavalent chromium remediation in groundwater within the effective range of the injection wells, and the SS rate of hexavalent chromium into trivalent chromium reached 94%-99.9%, the SS rate of total chromium fixation reached 83.9%-99.8%. The test results are of significant reference value for the remediation of contaminated sites with features of shallow groundwater depth and soil mainly consisting of silty clay and sandy clay.

40 CFR 421.154 - Standards of performance for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... ore as beryllium Beryllium 1,842.000 831.000 Chromium (total) 831.000 336.900 Copper 2,875.000 1,370... pounds) of beryllium carbonate produced from beryl ore as beryllium Beryllium 180.4 81.4 Chromium (total... beryllium carbonate produced as beryllium Beryllium 175.900 79.370 Chromium (total) 79.370 32.180 Copper 274...

40 CFR 420.124 - New source performance standards (NSPS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... Zinc 0.000376 0.000125 Chromium (hexavalent) 1 0.0000376 0.0000125 pH (2) (2) 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge wastewaters from the... product TSS 0.175 0.0751 O&G 0.0751 0.0250 Lead 0.00113 0.000376 Zinc 0.00150 0.000500 Chromium...

40 CFR 420.124 - New source performance standards (NSPS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... Zinc 0.000376 0.000125 Chromium (hexavalent) 1 0.0000376 0.0000125 pH (2) (2) 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge wastewaters from the... product TSS 0.175 0.0751 O&G 0.0751 0.0250 Lead 0.00113 0.000376 Zinc 0.00150 0.000500 Chromium...

40 CFR 420.124 - New source performance standards (NSPS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... Zinc 0.000376 0.000125 Chromium (hexavalent) 1 0.0000376 0.0000125 pH (2) (2) 1 The limitations for hexavalent chromium shall be applicable only to galvanizing operations which discharge wastewaters from the... product TSS 0.175 0.0751 O&G 0.0751 0.0250 Lead 0.00113 0.000376 Zinc 0.00150 0.000500 Chromium...

40 CFR 424.15 - Standards of performance for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... With Wet Air Pollution Control Devices Subcategory § 424.15 Standards of performance for new sources... values for 30 consecutive days shall not exceed— Metric units (kg/Mwh) TSS 0.024 0.012 Chromium total .0008 .0004 Chromium VI .00008 .00004 Manganese total .008 .0039 pH (1) (1) English units (lb/Mwh) TSS...

Reaction diffusion in the nickel-chromium-aluminum and cobalt-chromium-aluminum systems

NASA Technical Reports Server (NTRS)

Levine, S. R.

1977-01-01

The effects of MCrAl coating-substrate interdiffusion on oxidation life and the general mutliphase, multicomponent diffusion problem were examined. Semi-infinite diffusion couples that had sources representing coatings and sinks representing gas turbine alloys were annealed at 1,000, 1,095, 1,150, or 1,205 C for as long as 500 hours. The source and sink aluminum and chromium contents and the base metal (cobalt or nickel) determined the parabolic diffusion rate constants of the couples and predicted finite coating lives. The beta source strength concept provided a method (1) for correlating beta recession rate constants with composition; (2) for determining reliable average total, diffusion, and constitutional activation energies; and (3) for calculating interdiffusion coefficients.

Cadmium, lead, and chromium in large game: a local-scale exposure assessment for hunters consuming meat and liver of wild boar.

PubMed

Danieli, P P; Serrani, F; Primi, R; Ponzetta, M P; Ronchi, B; Amici, A

2012-11-01

Heavy metals are ubiquitous in soil, water, and air. Their entrance into the food chain is an important environmental issue that entails risks to humans. Several reports indicate that game meat can be an important source of heavy metals, particularly because of the increasing consumption of game meat, mainly by hunters. We performed an exposure assessment of hunters and members of their households, both adults and children, who consumed wild boar (WB) meat and offal. We estimated the amount of cadmium, lead, and chromium in the tissues of WB hunted in six areas within Viterbo Province (Italy) and gathered data on WB meat and offal consumption by conducting specific diet surveys in the same areas. The exposure to cadmium, lead, and chromium was simulated with specifically developed Monte Carlo simulation models. Cadmium and lead levels in WB liver and meat harvested in Viterbo Province (Italy) were similar to or lower than the values reported in other studies. However, some samples contained these metals at levels greater then the EU limits set for domestic animals. The chromium content of meat or liver cannot be evaluated against any regulatory limit, but our results suggest that the amounts of this metal found in WB products may reflect a moderate environmental load. Our survey of the hunter population confirmed that their consumption of WB meat and liver was greater than that of the general Italian population. This level of consumption was comparable with other European studies. Consumption of WB products contributes significantly to cadmium and lead exposure of both adults and children. More specifically, consumption of the WB liver contributed significantly to total cadmium and lead exposure of members of the households of WB hunters. As a general rule, liver consumption should be kept to a minimum, especially for children living in these hunter households. The exposure to chromium estimated for this population of hunters may be considered to be safe. However, a specific and complete assessment of chromium speciation in relevant dietary and environmental situations should be conducted.

Quantitative aspects of contact allergy to chromium and exposure to chrome-tanned leather.

PubMed

Hansen, Malene Barré; Rydin, Stefan; Menné, Torkil; Duus Johansen, Jeanne

2002-09-01

The potential of trivalent and hexavalent chromium to induce and elicit allergic contact dermatitis and the degree of chromium exposure from leather products are reviewed. Chromium dermatitis is often due to exposure in the occupational environment, with cement being one of the most common chromium sources. However, consumer products such as chromium(III)-tanned leather products are also an important source of chromium exposure. Apart from Cr(III), which is used for tanning, leather often also contains trace amounts of Cr(VI), which is formed by oxidation of Cr(III) during the tanning process. In a recent study of the Cr(VI) content of leather products bought on the Danish market, 35% of such articles had a Cr(VI) content above the detection limit of 3 p.p.m., ranging from 3.6 p.p.m. to 14.7 p.p.m. Leachable Cr(III) was detected at levels of 430-980 p.p.m. An examination of available dose-response studies showed that exposure to occluded patch test concentrations of 7-45 p.p.m. Cr(VI) elicits a reaction in 10% of the chromium-sensitive patients. When reviewing repeated open exposure studies, it is seen that either exposure to 5 p.p.m. Cr(VI) in the presence of 1% sodium lauryl sulfate (SLS) or exposure to 10 p.p.m. Cr(VI) alone both elicit eczema in chromium-sensitive patients. The eliciting capacity of Cr(III) has not been systematically investigated but, compared to Cr(VI), much higher concentrations are needed to elicit eczema.

40 CFR 421.324 - Standards of performance for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

.../kg (pounds per million pounds) of uranium processed in the refinery Chromium (total) 27.14 11.00... average mg/kg (pounds per million pounds) of uranium processed in the refinery Chromium (total) 1.689 0... Chromium (total) 2.357 0.955 Copper 8.152 3.885 Nickel 3.503 2.357 Fluoride 222.900 126.700 Total suspended...

40 CFR 421.326 - Pretreatment standards for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... uranium processed in the refinery Chromium (total) 27.14 11.00 Copper 93.88 44.74 Nickel 40.34 27.14... uranium processed in the refinery Chromium (total) 1.689 0.685 Copper 5.844 2.785 Nickel 2.511 1.689... per million pounds) of uranium processed in the refinery Chromium (total) 2.357 0.955 Copper 8.152 3...

40 CFR 471.35 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... (pounds per million off-pounds) of nickel-cobalt rolled with emulsions Chromium 0.063 0.026 Nickel 0.094 0... nickel-cobalt rolled with water Chromium 0.028 0.012 Nickel 0.042 0.028 Fluoride 4.49 1.99 (d) Tube... monthly average mg/off-kg (pounds per million off-pounds) of nickel-cobalt drawn with emulsions Chromium 0...

40 CFR 421.324 - Standards of performance for new sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

.../kg (pounds per million pounds) of uranium processed in the refinery Chromium (total) 27.14 11.00... average mg/kg (pounds per million pounds) of uranium processed in the refinery Chromium (total) 1.689 0... Chromium (total) 2.357 0.955 Copper 8.152 3.885 Nickel 3.503 2.357 Fluoride 222.900 126.700 Total suspended...

40 CFR 421.326 - Pretreatment standards for new sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

... uranium processed in the refinery Chromium (total) 27.14 11.00 Copper 93.88 44.74 Nickel 40.34 27.14... uranium processed in the refinery Chromium (total) 1.689 0.685 Copper 5.844 2.785 Nickel 2.511 1.689... per million pounds) of uranium processed in the refinery Chromium (total) 2.357 0.955 Copper 8.152 3...

40 CFR 420.85 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2014 CFR

2014-07-01

... daily values for 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 0.00292 0.00117... (pounds per 1,000 lb) of product Chromium 0.00175 0.000701 Nickel 0.00158 0.000526 (3) Batch, pipe and... Chromium 0.00709 0.00284 Nickel 0.00638 0.00213 (4) Continuous. Subpart H Pollutant or pollutant property...

40 CFR 420.106 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... (pounds per 1,000 lb) of product Chromium 1 0.0000209 0.0000084 Lead 0.0000094 0.0000031 Nickel 1 0... limitations for chromium and nickel shall be applicable in lieu of those for lead and zinc when cold rolling... Chromium 1 0.0000418 0.0000167 Lead 0.0000188 0.0000063 Nickel 1 0.0000376 0.0000125 Zinc 0.0000125 0...

40 CFR 420.106 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... (pounds per 1,000 lb) of product Chromium 1 0.0000209 0.0000084 Lead 0.0000094 0.0000031 Nickel 1 0... limitations for chromium and nickel shall be applicable in lieu of those for lead and zinc when cold rolling... Chromium 1 0.0000418 0.0000167 Lead 0.0000188 0.0000063 Nickel 1 0.0000376 0.0000125 Zinc 0.0000125 0...

40 CFR 420.85 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2013 CFR

2013-07-01

... daily values for 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 0.00292 0.00117... (pounds per 1,000 lb) of product Chromium 0.00175 0.000701 Nickel 0.00158 0.000526 (3) Batch, pipe and... Chromium 0.00709 0.00284 Nickel 0.00638 0.00213 (4) Continuous. Subpart H Pollutant or pollutant property...

40 CFR 420.85 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2012 CFR

2012-07-01

... daily values for 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 0.00292 0.00117... (pounds per 1,000 lb) of product Chromium 0.00175 0.000701 Nickel 0.00158 0.000526 (3) Batch, pipe and... Chromium 0.00709 0.00284 Nickel 0.00638 0.00213 (4) Continuous. Subpart H Pollutant or pollutant property...

40 CFR 420.106 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... (pounds per 1,000 lb) of product Chromium 1 0.0000209 0.0000084 Lead 0.0000094 0.0000031 Nickel 1 0... limitations for chromium and nickel shall be applicable in lieu of those for lead and zinc when cold rolling... Chromium 1 0.0000418 0.0000167 Lead 0.0000188 0.0000063 Nickel 1 0.0000376 0.0000125 Zinc 0.0000125 0...

40 CFR 420.86 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2013 CFR

2013-07-01

.../kkg (pounds per 1,000 lb) of product Chromium 0.00292 0.00117 Nickel 0.00263 0.000876 (2) Batch, rod... Chromium 0.00175 0.000701 Nickel 0.00158 0.000526 (3) Batch, pipe and tube. Subpart H Pollutant or... 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 0.00709 0.00284 Nickel 0.00638 0...

40 CFR 420.86 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2012 CFR

2012-07-01

.../kkg (pounds per 1,000 lb) of product Chromium 0.00292 0.00117 Nickel 0.00263 0.000876 (2) Batch, rod... Chromium 0.00175 0.000701 Nickel 0.00158 0.000526 (3) Batch, pipe and tube. Subpart H Pollutant or... 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 0.00709 0.00284 Nickel 0.00638 0...

40 CFR 420.86 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2014 CFR

2014-07-01

.../kkg (pounds per 1,000 lb) of product Chromium 0.00292 0.00117 Nickel 0.00263 0.000876 (2) Batch, rod... Chromium 0.00175 0.000701 Nickel 0.00158 0.000526 (3) Batch, pipe and tube. Subpart H Pollutant or... 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 0.00709 0.00284 Nickel 0.00638 0...

40 CFR 420.106 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... (pounds per 1,000 lb) of product Chromium 1 0.0000209 0.0000084 Lead 0.0000094 0.0000031 Nickel 1 0... limitations for chromium and nickel shall be applicable in lieu of those for lead and zinc when cold rolling... Chromium 1 0.0000418 0.0000167 Lead 0.0000188 0.0000063 Nickel 1 0.0000376 0.0000125 Zinc 0.0000125 0...

40 CFR 467.36 - Pretreatment standards for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... day Maximum for monthly average mg/off-kg (lb/million off-lbs) of extruded Chromium 0.13 0.05 Cyanide... monthly average mg/off-kg (lb/million off-lbs) of hard alloy aluminum extruded Chromium 0.11 0.05 Cyanide... day Maximum for monthly average mg/off-kg (lb/million off-lbs) of aluminum cast Chromium 0.49 0.20...

40 CFR 420.106 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... (pounds per 1,000 lb) of product Chromium 1 0.0000209 0.0000084 Lead 0.0000094 0.0000031 Nickel 1 0... limitations for chromium and nickel shall be applicable in lieu of those for lead and zinc when cold rolling... Chromium 1 0.0000418 0.0000167 Lead 0.0000188 0.0000063 Nickel 1 0.0000376 0.0000125 Zinc 0.0000125 0...

Acute stent recoil and optimal balloon inflation strategy: an experimental study using real-time optical coherence tomography.

PubMed

Kitahara, Hideki; Waseda, Katsuhisa; Yamada, Ryotaro; Otagiri, Kyuhachi; Tanaka, Shigemitsu; Kobayashi, Yuhei; Okada, Kozo; Kume, Teruyoshi; Nakagawa, Kaori; Teramoto, Tomohiko; Ikeno, Fumiaki; Yock, Paul G; Fitzgerald, Peter J; Honda, Yasuhiro

2016-06-12

Our aim was to evaluate stent expansion and acute recoil at deployment and post-dilatation, and the impact of post-dilatation strategies on final stent dimensions. Optical coherence tomography (OCT) was performed on eight bare metal platforms of drug-eluting stents (3.0 mm diameter, n=6 for each) during and after balloon inflation in a silicone mock vessel. After nominal-pressure deployment, a single long (30 sec) vs. multiple short (10 sec x3) post-dilatations were performed using a non-compliant balloon (3.25 mm, 20 atm). Stent areas during deployment with original delivery systems were smaller in stainless steel stents than in cobalt-chromium and platinum-chromium stents (p<0.001), whereas subsequent acute recoil was comparable among the three materials. At post-dilatation, acute recoil was greater in cobalt-chromium and platinum-chromium stents than in stainless steel stents (p<0.001), resulting in smaller final stent areas in cobalt-chromium and platinum-chromium stents than in stainless steel stents (p<0.001). In comparison between conventional and latest-generation cobalt-chromium stents, stent areas were not significantly different after both deployment and post-dilatation. With multiple short post-dilatations, acute recoil was significantly improved from first to third short inflation (p<0.001), achieving larger final area than a single long inflation, despite stent materials/designs (p<0.001). Real-time OCT revealed significant acute recoil in all stent types. Both stent materials/designs and post-dilatation strategies showed a significant impact on final stent expansion.

40 CFR 471.93 - New source performance standards (NSPS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... monthly average mg/off-kg (pounds per million off-pounds) of zirconium-hafnium extruded Chromium 0.104 0... monthly average mg/off-kg (pounds per million off-pounds) of zirconium-hafnium heat treated Chromium 0.015... Chromium 0.150 0.061 Cyanide 0.099 0.041 Nickel 0.653 0.432 Ammonia 45.3 20.0 Fluoride 20.0 8.98 Oil and...

40 CFR 471.34 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2011 CFR

2011-07-01

... emulsions Chromium 0.063 0.026 Nickel 0.094 0.063 Fluoride 10.1 4.49 (c) Rolling contact cooling water... (pounds per million off-pounds) of nickel-cobalt rolled with water Chromium 0.028 0.011 Nickel 0.042 0.028... drawn with emulsions Chromium 0.036 0.014 Nickel 0.053 0.036 Fluoride 5.68 2.52 (g) Extrusion spent...

40 CFR 471.93 - New source performance standards (NSPS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... monthly average mg/off-kg (pounds per million off-pounds) of zirconium-hafnium extruded Chromium 0.104 0... monthly average mg/off-kg (pounds per million off-pounds) of zirconium-hafnium heat treated Chromium 0.015... Chromium 0.150 0.061 Cyanide 0.099 0.041 Nickel 0.653 0.432 Ammonia 45.3 20.0 Fluoride 20.0 8.98 Oil and...

Life Cycle Assessment for PC Blend 2 Aircraft Radome Depainter

DTIC Science & Technology

1996-09-01

Trivalent chromium compounds are considerably less toxic than hexavalent forms and are neither irritating nor corrosive. 25. IRON (W) Ecosystem: Visibility...acquisition and combustion is a source of waterborne acid, ammonia, BOD, chromium , COD, dissolved solids, iron, lead, metal ion, oil, phenol...intermediates for DBE. Chromium , phenol, zinc, and COD process emissions come from petroleum refinery operations. The production of ammonia also produces

40 CFR 468.15 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

...-pounds of copper or copper alloy hot rolled Chromium 0.038 0.015 Copper 0.131 0.062 Lead 0.010 0.0092... English units—pounds per 1,000,000 off-pounds of copper or copper alloy cold rolled Chromium 0.140 0.056... copper alloy drawn English units—pounds per 1,000,000 off-pounds of copper or copper alloy drawn Chromium...

40 CFR 420.105 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2012 CFR

2012-07-01

... for 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 1 0.0000209 0.0000084 Lead 0... Tetrachloroethylene 0.0000031 1 The limitations for chromium and nickel shall be applicable in lieu of those for lead... (pounds per 1,000 lb) of product Chromium 1 0.000104 0.0000418 Lead 0.0000469 0.0000156 Nickel 1 0.0000939...

40 CFR 421.306 - Pretreatment standards for new sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

... average mg/kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122... Maximum for monthly average mg/kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.385 0... for any 1 day Maximum for monthly average mg/kg (pounds per million pounds) of TiCl4 handled Chromium...

Electrodeposition of amorphous ternary nickel-chromium-phosphorus alloy

DOEpatents

Guilinger, Terry R.

1990-01-01

Amorphous ternary nickel-chromium-phosphorus alloys are electrodeposited from a bath comprising a nickel salt, a chromium salt, a phosphorus source such as sodium hypophosphite, a complexing agent for the nickel ions, supporting salts to increase conductivity, and a buffering agent. The process is carried out at about room temperature and requires a current density between about 20 to 40 A/dm.sup.2.

40 CFR 421.306 - Pretreatment standards for new sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

... average mg/kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122... Maximum for monthly average mg/kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.385 0... for any 1 day Maximum for monthly average mg/kg (pounds per million pounds) of TiCl4 handled Chromium...

40 CFR 420.105 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2013 CFR

2013-07-01

... for 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 1 0.0000209 0.0000084 Lead 0... Tetrachloroethylene 0.0000031 1 The limitations for chromium and nickel shall be applicable in lieu of those for lead... (pounds per 1,000 lb) of product Chromium 1 0.000104 0.0000418 Lead 0.0000469 0.0000156 Nickel 1 0.0000939...

40 CFR 420.105 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2014 CFR

2014-07-01

... for 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 1 0.0000209 0.0000084 Lead 0... Tetrachloroethylene 0.0000031 1 The limitations for chromium and nickel shall be applicable in lieu of those for lead... (pounds per 1,000 lb) of product Chromium 1 0.000104 0.0000418 Lead 0.0000469 0.0000156 Nickel 1 0.0000939...

40 CFR 421.306 - Pretreatment standards for new sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

... average mg/kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122... Maximum for monthly average mg/kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.385 0... for any 1 day Maximum for monthly average mg/kg (pounds per million pounds) of TiCl4 handled Chromium...

40 CFR 420.105 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2010 CFR

2010-07-01

... for 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 1 0.0000209 0.0000084 Lead 0... Tetrachloroethylene 0.0000031 1 The limitations for chromium and nickel shall be applicable in lieu of those for lead... (pounds per 1,000 lb) of product Chromium 1 0.000104 0.0000418 Lead 0.0000469 0.0000156 Nickel 1 0.0000939...

40 CFR 420.105 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2011 CFR

2011-07-01

... for 30 consecutive days Kg/kkg (pounds per 1,000 lb) of product Chromium 1 0.0000209 0.0000084 Lead 0... Tetrachloroethylene 0.0000031 1 The limitations for chromium and nickel shall be applicable in lieu of those for lead... (pounds per 1,000 lb) of product Chromium 1 0.000104 0.0000418 Lead 0.0000469 0.0000156 Nickel 1 0.0000939...

40 CFR 467.35 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... extruded Chromium 0.15 0.061 Cyanide 0.098 0.041 Zinc 0.49 0.21 TTO 0.23 Oil and grease (alternate... for any 1 day Maximum for monthly average mg/off-kg (lb/million off-lbs) of extruded Chromium 0.65 0... 1 day Maximum for monthly average mg/off-kg (lb/million off-lbs) of aluminum cast Chromium 0.59 0.24...

40 CFR 467.16 - Pretreatment standards for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... Maximum for monthly average mg/off-kg (lb/million off-lbs) of aluminum rolled with neat oils Chromium 0... rolled with neat oils Chromium 0.021 0.009 Cyanide 0.011 0.005 Zinc 0.057 0.024 TTO 0.038 Oil and grease... aluminum cast Chromium 0.00073 0.00029 Cyanide 0.00039 0.00016 Zinc 0.0020 0.00082 TTO 0.0014 Oil and...

Hypoglycemic potency of novel trivalent chromium in hyperglycemic insulin-deficient rats.

PubMed

Machaliński, Bogusław; Walczak, Mieczysław; Syrenicz, Anhelli; Machalińska, Anna; Grymuła, Katarzyna; Stecewicz, Iwona; Wiszniewska, Barbara; Dabkowska, Elzbieta

2006-01-01

Two sources of chromium III, "chromium 454" and "chromium picolinate," were tested in insulin-deficient Streptozocin-treated diabetic rats. This model was selected in order to evaluate the possibility of any hypoglycemic potency of chromium in a relative absence of blood insulin concentration. Three weeks of the treatment with CRC454 and CrP resulted in a 38% and 11% reduction of blood glucose levels, respectively. Body weight gains were equally improved by both treatments. Blood levels of CK, ALT and AST were significantly reduced by CRC454 and CrP. These results might suggest that any hypoglycemic effect of trivalent chromium under insulin-deficient conditions could be largely dependent upon the type of chromium agent and associated characteristics such as solubility and bioavalibility. In contrast, improvement of body weight gains and blood levels of CK, AST and ALT seems to be less dependent on the type of chromium compound under these experimental conditions. In conclusion, CRC454 showed significant reduction of hyperglycemia under insulin-deficient conditions.

Paragenesis of Cr-rich muscovite and chlorite in green-mica quartzites of Saigaon-Palasgaon area, Western Bastar Craton, India

NASA Astrophysics Data System (ADS)

Randive, K. R.; Korakoppa, M. M.; Muley, S. V.; Varade, A. M.; Khandare, H. W.; Lanjewar, S. G.; Tiwari, R. R.; Aradhi, K. K.

2015-02-01

Green mica (fuchsite or chromian-muscovite) is reported worldwide in the Archaean metasedimentary rocks, especially quartzites. They are generally associated with a suite of heavy minerals and a range of phyllosilicates. We report the occurrence of green-mica quartzites in the Saigaon-Palasgaon area within Bastar Craton in central India. Mineralogical study has shown that there are two types of muscovites; the chromium-containing muscovite (Cr2O3 0.84-1.84%) and muscovite (Cr2O3 0.00-0.22%). Chlorites are chromium-containing chlorites (Cr2O3 3.66-5.39%) and low-chromium-containing chlorites (Cr2O3 0.56-2.62%), and as such represent ripidolite-brunsvigite varieties. Back scattered electron images and EPMA data has revealed that chlorite occurs in two forms, viz., parallel to subparallel stacks in the form of intergrowth with muscovite and independent crystals within the matrix. The present study indicates that the replacement of chromium-containing chlorite by chromium-containing muscovite is found to be due to increasing grade of metamorphism of chromium-rich sediments. However, the absence of significant compositional gap between aforementioned varieties indicates disparate substitution of cations, especially chromium, within matrix chlorites. The chromium-containing muscovite and muscovite are two separate varieties having distinct paragenesis.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Izbicki, John A.; Wright, Michael T.; Seymour, Whitney A.

Hexavalent chromium, Cr(VI), in 918 wells sampled throughout California between 2004 and 2012 by the Groundwater Ambient Monitoring and Assessment Program—Priority Basin Project (GAMA—PBP) ranged from less than the study reporting limit (SRL) of 1 microgram per liter (μg/L) to 32 μg/L. Statewide, Cr(VI) was reported in 31 percent of sampled wells and equaled or exceeded the recently established (2014) California Maximum Contaminant Level (MCL) for Cr(VI) of 10 μg/L in 4 percent of sampled wells. Cr(VI) data collected for regulatory purposes overestimate Cr(VI) occurrence. Ninety percent of chromium was present as Cr(VI), which was detected more frequently and atmore » higher concentrations in alkaline (pH > 8), oxic water, and more frequently in agricultural and urban land uses compared to native land uses. Chemical, isotopic (tritium and carbon-14), and noble-gas data show high Cr(VI) in water from wells in alluvial aquifers in the southern California deserts result from long groundwater-residence times and geochemical reactions such as silicate weathering that increase pH, while oxic conditions persist. High Cr(VI) in water from wells in alluvial aquifers along the west-side of the Central Valley results from high-chromium abundance in source rock eroded to form those aquifers, and areal recharge processes (including irrigation return) that mobilize chromium from the unsaturated zone. Cr(VI) co-occurred with oxyanions having similar chemistry, including vanadium, selenium, and uranium. Cr(VI) was positively correlated with nitrate, consistent with increased concentrations in areas of agricultural land use and mobilization of chromium from the unsaturated zone by irrigation return.« less

40 CFR 471.25 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... million off-pounds) of magnesium rolled with emulsions Chromium 0.028 0.011 Zinc 0.076 0.032 Ammonia 9.95... forged magnesium cooled with water Chromium 0.107 0.044 Zinc 0.295 0.122 Ammonia 38.5 17.0 Fluoride 17.2... forged Chromium 0.002 0.0006 Zinc 0.004 0.002 Ammonia 0.532 0.234 Fluoride 0.238 0.106 (e) Direct chill...

40 CFR 471.25 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... million off-pounds) of magnesium rolled with emulsions Chromium 0.028 0.011 Zinc 0.076 0.032 Ammonia 9.95... forged magnesium cooled with water Chromium 0.107 0.044 Zinc 0.295 0.122 Ammonia 38.5 17.0 Fluoride 17.2... forged Chromium 0.002 0.0006 Zinc 0.004 0.002 Ammonia 0.532 0.234 Fluoride 0.238 0.106 (e) Direct chill...

40 CFR 471.25 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... million off-pounds) of magnesium rolled with emulsions Chromium 0.028 0.011 Zinc 0.076 0.032 Ammonia 9.95... forged magnesium cooled with water Chromium 0.107 0.044 Zinc 0.295 0.122 Ammonia 38.5 17.0 Fluoride 17.2... forged Chromium 0.002 0.0006 Zinc 0.004 0.002 Ammonia 0.532 0.234 Fluoride 0.238 0.106 (e) Direct chill...

40 CFR 471.25 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... million off-pounds) of magnesium rolled with emulsions Chromium 0.028 0.011 Zinc 0.076 0.032 Ammonia 9.95... forged magnesium cooled with water Chromium 0.107 0.044 Zinc 0.295 0.122 Ammonia 38.5 17.0 Fluoride 17.2... forged Chromium 0.002 0.0006 Zinc 0.004 0.002 Ammonia 0.532 0.234 Fluoride 0.238 0.106 (e) Direct chill...

40 CFR 471.25 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... million off-pounds) of magnesium rolled with emulsions Chromium 0.028 0.011 Zinc 0.076 0.032 Ammonia 9.95... forged magnesium cooled with water Chromium 0.107 0.044 Zinc 0.295 0.122 Ammonia 38.5 17.0 Fluoride 17.2... forged Chromium 0.002 0.0006 Zinc 0.004 0.002 Ammonia 0.532 0.234 Fluoride 0.238 0.106 (e) Direct chill...

40 CFR 471.23 - New source performance standards (NSPS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... million off-pounds) of magnesium rolled with emulsions Chromium 0.028 0.011 Zinc 0.076 0.032 Ammonia 9.95... forged magnesium cooled with water Chromium 0.107 0.044 Zinc 0.295 0.122 Ammonia 38.5 17.0 Fluoride 17.2... forged Chromium 0.002 0.0006 Zinc 0.004 0.002 Ammonia 0.532 0.234 Fluoride 0.238 0.106 Oil and grease 0...

40 CFR 468.13 - New source performance standards (NSPS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... copper alloy hot rolled Chromium 0.038 0.015 Copper 0.131 0.062 Lead 0.010 0.0092 Nickel 0.056 0.038 Zinc... rolled English units—pounds per 1,000,000 off-pounds of copper or copper alloy cold rolled Chromium 0.140... copper or copper alloy drawn Chromium 0.031 0.012 Copper 0.108 0.051 Lead 0.0085 0.0076 Nickel 0.046 0...

40 CFR 468.13 - New source performance standards (NSPS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... copper alloy hot rolled Chromium 0.038 0.015 Copper 0.131 0.062 Lead 0.010 0.0092 Nickel 0.056 0.038 Zinc... rolled English units—pounds per 1,000,000 off-pounds of copper or copper alloy cold rolled Chromium 0.140... copper or copper alloy drawn Chromium 0.031 0.012 Copper 0.108 0.051 Lead 0.0085 0.0076 Nickel 0.046 0...

40 CFR 468.13 - New source performance standards (NSPS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... copper alloy hot rolled Chromium 0.038 0.015 Copper 0.131 0.062 Lead 0.010 0.0092 Nickel 0.056 0.038 Zinc... rolled English units—pounds per 1,000,000 off-pounds of copper or copper alloy cold rolled Chromium 0.140... copper or copper alloy drawn Chromium 0.031 0.012 Copper 0.108 0.051 Lead 0.0085 0.0076 Nickel 0.046 0...

40 CFR 421.305 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

... pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496.../kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.385 0.156 Lead 0.291 0.135 Nickel... monthly average mg/kg (pounds per million pounds) of TiCl4 handled Chromium (total) 0.069 0.028 Lead 0.052...

40 CFR 420.104 - New source performance standards (NSPS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... TSS 0.00125 0.000626 O&G 0.000522 0.000209 Chromium 1 0.0000209 0.0000084 Lead 0.0000094 0.0000031... pH (2) (2) 1 The limitations for chromium and nickel shall be applicable in lieu of those for lead... consecutive days Kg/kkg (pounds per 1,000 lb) of product TSS 0.00250 0.00125 O&G 0.00104 0.000417 Chromium 1 0...

40 CFR 421.305 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

... pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496.../kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.385 0.156 Lead 0.291 0.135 Nickel... monthly average mg/kg (pounds per million pounds) of TiCl4 handled Chromium (total) 0.069 0.028 Lead 0.052...

40 CFR 420.104 - New source performance standards (NSPS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... TSS 0.00125 0.000626 O&G 0.000522 0.000209 Chromium 1 0.0000209 0.0000084 Lead 0.0000094 0.0000031... pH (2) (2) 1 The limitations for chromium and nickel shall be applicable in lieu of those for lead... consecutive days Kg/kkg (pounds per 1,000 lb) of product TSS 0.00250 0.00125 O&G 0.00104 0.000417 Chromium 1 0...

40 CFR 420.104 - New source performance standards (NSPS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... TSS 0.00125 0.000626 O&G 0.000522 0.000209 Chromium 1 0.0000209 0.0000084 Lead 0.0000094 0.0000031... pH (2) (2) 1 The limitations for chromium and nickel shall be applicable in lieu of those for lead... consecutive days Kg/kkg (pounds per 1,000 lb) of product TSS 0.00250 0.00125 O&G 0.00104 0.000417 Chromium 1 0...

40 CFR 421.305 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

... pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496.../kg (pounds per million pounds) of TiCl4 produced Chromium (total) 0.385 0.156 Lead 0.291 0.135 Nickel... monthly average mg/kg (pounds per million pounds) of TiCl4 handled Chromium (total) 0.069 0.028 Lead 0.052...

40 CFR 467.15 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... aluminum rolled with neat oils Chromium 0.036 0.015 Cyanide 0.024 0.010 Zinc 0.119 0.050 TTO 0.057 Oil and... off-lbs) of aluminum rolled with neat oils Chromium 0.025 0.010 Cyanide 0.016 0.007 Zinc 0.081 0.034... (lb/million off-lbs) of aluminum cast Chromium 0.00086 0.00035 Cyanide 0.00057 0.00024 Zinc 0.0029 0...

40 CFR 420.104 - New source performance standards (NSPS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... TSS 0.00125 0.000626 O&G 0.000522 0.000209 Chromium 1 0.0000209 0.0000084 Lead 0.0000094 0.0000031... pH (2) (2) 1 The limitations for chromium and nickel shall be applicable in lieu of those for lead... consecutive days Kg/kkg (pounds per 1,000 lb) of product TSS 0.00250 0.00125 O&G 0.00104 0.000417 Chromium 1 0...

40 CFR 420.104 - New source performance standards (NSPS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... TSS 0.00125 0.000626 O&G 0.000522 0.000209 Chromium 1 0.0000209 0.0000084 Lead 0.0000094 0.0000031... pH (2) (2) 1 The limitations for chromium and nickel shall be applicable in lieu of those for lead... consecutive days Kg/kkg (pounds per 1,000 lb) of product TSS 0.00250 0.00125 O&G 0.00104 0.000417 Chromium 1 0...

Anthropogenic Chromium Emissions in China from 1990 to 2009

PubMed Central

Cheng, Hongguang; Zhou, Tan; Li, Qian; Lu, Lu; Lin, Chunye

2014-01-01

An inventory of chromium emission into the atmosphere and water from anthropogenic activities in China was compiled for 1990 through to 2009. We estimate that the total emission of chromium to the atmosphere is about 1.92×105t. Coal and oil combustion were the two leading sources of chromium emission to the atmosphere in China, while the contribution of them showed opposite annual growth trend. In total, nearly 1.34×104t of chromium was discharged to water, mainly from six industrial categories in 20 years. Among them, the metal fabrication industry and the leather tanning sector were the dominant sources of chromium emissions, accounting for approximately 68.0% and 20.0% of the total emissions and representing increases of15.6% and 10.3% annually, respectively. The spatial trends of Cr emissions show significant variation based on emissions from 2005 to 2009. The emission to the atmosphere was heaviest in Hebei, Shandong, Guangdong, Zhejiang and Shanxi, whose annual emissions reached more than 1000t for the high level of coal and oil consumption. In terms of emission to water, the largest contributors were Guangdong, Jiangsu, Shandong and Zhejiang, where most of the leather production and metal manufacturing occur and these four regions accounted for nearly 47.4% of the total emission to water. PMID:24505309

Insulin sensitising action of chromium picolinate in various experimental models of diabetes mellitus.

PubMed

Shindea, Urmila A; Sharma, Geeta; Xu, Yan J; Dhalla, Naranjan S; Goyal, Ramesh K

2004-01-01

Although chromium is an essential element for carbohydrate and lipid metabolism, its effects in diabetic patients are still debated. We have studied the effect of 6 week treatment with chromium picolinate (8 microg/ml in drinking water) in streptozotocin (STZ)-induced type 1 and type 2 diabetic rat models. The mechanism of anti-diabetic action of chromium picolinate was studied using C2C12 myoblasts and 3T3-L1 adipocytes. Chromium picolinate significantly decreased the area under the curve over 120 min for glucose of both STZ-induced type 1 (40mg/kg, i.v. in adult rats) and type 2 (90 mg/kg, i.p. in 2 day old rat neonates) diabetic rats without any significant change in area under the curve over 120 min for insulin as compared to controls. The composite insulin sensitivity index and insulin sensitivity index (KITT) values of both type 1 and type 2 diabetic rats were increased significantly by chromium picolinate. Treatment with chromium picolinate produced a significant decrease in elevated cholesterol and triglyceride levels in both types of diabetic rats. In 3T3-L1 adipocytes, chromium picolinate (0-10 micromol) per se did not produce any effect, however, when co-incubated with insulin it significantly increased the intracellular triglyceride synthesis (EC50 = 363.7nmol/1). Similarly in C2C12 myoblasts, chromium picolinate alone did not produce any effect, however, it significantly increased insulin-induced transport of 14C-glucose. In conclusion, chromium picolinate significantly improves deranged carbohydrate and lipid metabolism of experimental chemically induced diabetes in rats. The mechanism of in vivo anti-diabetic action appears to be peripheral (skeletal muscle and adipose tissue) insulin enhancing action of chromium.

Assessment of chromium and nickel levels in surface sea waters and sediments from industrial marine area in Tuzla Aydinli Bay, Istanbul Turkey.

PubMed

Baysal, Asli; Akman, Suleyman

2018-05-01

The determination and evaluation of nickel and chromium in Tuzla Aydinli Bay is an important subject since it is an industrial marine area for decades and it is crucial to protect aquatic life which are toxic for the aqueous environment. In this study, 32 samples were collected both from near the coastal shipyard activity to far of the activity areas in Tuzla Aydinli Bay, Istanbul (Turkey) according to the standard guidance. Nickel and chromium were determined in the sea water and sediment samples by graphite furnace atomic absorption spectrometry. The contamination factors and geoaccumulation indices with respect to nickel and chromium were calculated and evaluated. Based on the modified ecological risk assessments, variable results were obtained depending on the selection of control (blank) points. Copyright © 2018 Elsevier Ltd. All rights reserved.

Large scale groundwater flow and hexavalent chromium transport modeling under current and future climatic conditions: the case of Asopos River Basin.

PubMed

Dokou, Zoi; Karagiorgi, Vasiliki; Karatzas, George P; Nikolaidis, Nikolaos P; Kalogerakis, Nicolas

2016-03-01

In recent years, high concentrations of hexavalent chromium, Cr(VI), have been observed in the groundwater system of the Asopos River Basin, raising public concern regarding the quality of drinking and irrigation water. The work described herein focuses on the development of a groundwater flow and Cr(VI) transport model using hydrologic, geologic, and water quality data collected from various sources. An important dataset for this goal comprised an extensive time series of Cr(VI) concentrations at various locations that provided an indication of areas of high concentration and also served as model calibration locations. Two main sources of Cr(VI) contamination were considered in the area: anthropogenic contamination originating from Cr-rich industrial wastes buried or injected into the aquifer and geogenic contamination from the leaching process of ophiolitic rocks. The aquifer's response under climatic change scenario A2 was also investigated for the next two decades. Under this scenario, it is expected that rainfall, and thus infiltration, will decrease by 7.7 % during the winter and 15 % during the summer periods. The results for two sub-scenarios (linear and variable precipitation reduction) that were implemented based on A2 show that the impact on the study aquifer is moderate, resulting in a mean level decrease less than 1 m in both cases. The drier climatic conditions resulted in higher Cr(VI) concentrations, especially around the industrial areas.

40 CFR 424.35 - Standards of performance for new sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

...— Metric units (kg/kkg processed) TSS 0.271 0.136 Chromium total .0054 .0027 Manganese total 0.054 .027 pH (1) (1) English units (lb/ton processed) TSS .542 .271 Chromium total .011 .0054 Manganese total .108...

40 CFR 424.35 - Standards of performance for new sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

...— Metric units (kg/kkg processed) TSS 0.271 0.136 Chromium total .0054 .0027 Manganese total 0.054 .027 pH (1) (1) English units (lb/ton processed) TSS .542 .271 Chromium total .011 .0054 Manganese total .108...

40 CFR 424.35 - Standards of performance for new sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

...— Metric units (kg/kkg processed) TSS 0.271 0.136 Chromium total .0054 .0027 Manganese total 0.054 .027 pH (1) (1) English units (lb/ton processed) TSS .542 .271 Chromium total .011 .0054 Manganese total .108...

40 CFR 424.35 - Standards of performance for new sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

...— Metric units (kg/kkg processed) TSS 0.271 0.136 Chromium total .0054 .0027 Manganese total 0.054 .027 pH (1) (1) English units (lb/ton processed) TSS .542 .271 Chromium total .011 .0054 Manganese total .108...

40 CFR 424.35 - Standards of performance for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

...— Metric units (kg/kkg processed) TSS 0.271 0.136 Chromium total .0054 .0027 Manganese total 0.054 .027 pH (1) (1) English units (lb/ton processed) TSS .542 .271 Chromium total .011 .0054 Manganese total .108...

40 CFR 471.94 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2011 CFR

2011-07-01

...-hafnium extruded Chromium 0.104 0.043 Cyanide 0.069 0.029 Nickel 0.455 0.301 Ammonia 31.6 13.9 Fluoride 14...-hafnium heat treated Chromium 0.015 0.006 Cyanide 0.010 0.004 Nickel 0.066 0.044 Ammonia 4.57 2.01...-hafnium surface treated Chromium 0.150 0.061 Cyanide 0.099 0.041 Nickel 0.653 0.432 Ammonia 45.3 20.0...

40 CFR 471.75 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... (pounds per million off-pounds) of uranium extruded Cadmium 0.007 0.003 Chromium 0.013 0.005 Copper 0.044... treated Cadmium 0.006 0.003 Chromium 0.012 0.005 Copper 0.040 0.019 Lead 0.009 0.004 Nickel 0.017 0.012...-pounds) of uranium surface treated Cadmium 0.006 0.002 Chromium 0.010 0.004 Copper 0.035 0.017 Lead 0.008...

40 CFR 471.75 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... (pounds per million off-pounds) of uranium extruded Cadmium 0.007 0.003 Chromium 0.013 0.005 Copper 0.044... treated Cadmium 0.006 0.003 Chromium 0.012 0.005 Copper 0.040 0.019 Lead 0.009 0.004 Nickel 0.017 0.012...-pounds) of uranium surface treated Cadmium 0.006 0.002 Chromium 0.010 0.004 Copper 0.035 0.017 Lead 0.008...

40 CFR 471.95 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... extruded Chromium 0.104 0.043 Cyanide 0.069 0.029 Nickel 0.455 0.301 Ammonia 31.6 13.9 Fluoride 14.1 6.26...-hafnium heat treated Chromium 0.015 0.006 Cyanide 0.010 0.004 Nickel 0.066 0.044 Ammonia 4.57 2.01...-hafnium surface treated Chromium 0.150 0.061 Cyanide 0.099 0.041 Nickel 0.653 0.432 Ammonia 45.3 20...

40 CFR 471.95 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... extruded Chromium 0.104 0.043 Cyanide 0.069 0.029 Nickel 0.455 0.301 Ammonia 31.6 13.9 Fluoride 14.1 6.26...-hafnium heat treated Chromium 0.015 0.006 Cyanide 0.010 0.004 Nickel 0.066 0.044 Ammonia 4.57 2.01...-hafnium surface treated Chromium 0.150 0.061 Cyanide 0.099 0.041 Nickel 0.653 0.432 Ammonia 45.3 20...

40 CFR 471.94 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2010 CFR

2010-07-01

...-hafnium extruded Chromium 0.104 0.043 Cyanide 0.069 0.029 Nickel 0.455 0.301 Ammonia 31.6 13.9 Fluoride 14...-hafnium heat treated Chromium 0.015 0.006 Cyanide 0.010 0.004 Nickel 0.066 0.044 Ammonia 4.57 2.01...-hafnium surface treated Chromium 0.150 0.061 Cyanide 0.099 0.041 Nickel 0.653 0.432 Ammonia 45.3 20.0...

Special Advanced Studies for Pollution Prevention. Delivery Order 0065: The Monitor - Spring 2001

DTIC Science & Technology

2001-06-01

coating) baths by remov- ing trace contaminant metals as well as restoring and maintaining the hexavalent chromium or ferric species. The oxidizing...power for the process acid is restored by oxidation (trivalent chromium to hexavalent chromium or ferrous to ferric) at the anode. Other sources of...selection to the application. UF membranes are suitable for particles in the molecular range of 0.1-0.01microns. Microfiltration membranes are similar

40 CFR 468.14 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2011 CFR

2011-07-01

... per 1,000,000 off-pounds of copper or copper alloy hot rolled Chromium 0.045 0.018 Copper 0.195 0.103... rolled English units—pounds per 1,000,000 off-pounds of copper or copper alloy cold rolled Chromium 0.166... drawn Chromium 0.037 0.015 Copper 0.161 0.085 Lead 0.012 0.011 Nickel 0.163 0.107 Zinc 0.124 0.051 TTO 0...

40 CFR 468.14 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2013 CFR

2013-07-01

... rolled English units—pounds per 1,000,000 off-pounds of copper or copper alloy hot rolled Chromium 0.045... alloy cold rolled Chromium 0.166 0.068 Copper 0.720 0.379 Lead 0.056 0.049 Nickel 0.727 0.481 Zinc 0.553... copper or copper alloy drawn Chromium 0.037 0.015 Copper 0.161 0.085 Lead 0.012 0.011 Nickel 0.163 0.107...

40 CFR 468.14 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2014 CFR

2014-07-01

... rolled English units—pounds per 1,000,000 off-pounds of copper or copper alloy hot rolled Chromium 0.045... alloy cold rolled Chromium 0.166 0.068 Copper 0.720 0.379 Lead 0.056 0.049 Nickel 0.727 0.481 Zinc 0.553... copper or copper alloy drawn Chromium 0.037 0.015 Copper 0.161 0.085 Lead 0.012 0.011 Nickel 0.163 0.107...

40 CFR 468.14 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2012 CFR

2012-07-01

... rolled English units—pounds per 1,000,000 off-pounds of copper or copper alloy hot rolled Chromium 0.045... alloy cold rolled Chromium 0.166 0.068 Copper 0.720 0.379 Lead 0.056 0.049 Nickel 0.727 0.481 Zinc 0.553... copper or copper alloy drawn Chromium 0.037 0.015 Copper 0.161 0.085 Lead 0.012 0.011 Nickel 0.163 0.107...

Chromium (V) compounds as cathode material in electrochemical power sources

DOEpatents

Delnick, F.M.; Guidotti, R.A.; McCarthy, D.K.

A cathode for use in a thermal battery, comprising a chromium (V) compound. The preferred materials for this use are Ca/sub 5/(CrO/sub 4/)/sub 3/Cl, Ca/sub 5/(CrO/sub 4/)OH, and Cr/sub 2/O/sub 5/. The chromium (V) compound can be employed as a cathode material in ambient temperature batteries when blended with a suitably conductive filler, preferably carbon black.

Chromium (V) compounds as cathode material in electrochemical power sources

DOEpatents

Delnick, Frank M.; Guidotti, Ronald A.; McCarthy, David K.

1985-01-01

A cathode for use in a thermal battery, comprising a chromium (V) compound. The preferred materials for this use are Ca.sub.5 (CrO.sub.4).sub.3 Cl, Ca.sub.5 (CrO.sub.4).sub.3 OH, and Cr.sub.2 O.sub.5. The chromium (V) compound can be employed as a cathode material in ambient temperature batteries when blended with a suitably conductive filler, preferably carbon black.

Supplemental Groundwater Remediation Technologies to Protect the Columbia River at Hanford, WA

DOE Office of Scientific and Technical Information (OSTI.GOV)

Thompson, K. M.; Petersen, Scott W.; Fruchter, Jonathan S.

2007-12-15

Nine projects have been recently selected by the US Department of Energy (EM-22) to address groundwater contaminant migration at the Hanford Site. This paper summarizes the background and objectives of these projects. Five of the selected projects are targeted at hexavalent chromium contamination in Hanford 100 Area groundwater. These projects represent an integrated approach towards identifying the source of hexavalent chromium contamination in the Hanford 100-D Area and treating the groundwater contamination. Currently, there is no effective method to stop strontium-90 associated with the riparian zone sediments from leaching into the river. Phytoremediation may be a possible way to treatmore » this contamination. Its use at the 100-N Area will be investigated. Another technology currently being tested for strontium-90 contamination at the 100-N Area involves injection (through wells) of a calcium-citrate-phosphate solution, which will precipitate apatite, a natural calcium-phosphate mineral. Apatite will adsorb the strontium-90, and then incorporate it as part of the apatite structure, isolating the strontium-90 contamination from entering the river. This EM-22 funded apatite project will develop a strategy for infiltrating the apatite solution from ground surface or a shallow trench to provide treatment over the upper portion of the contaminated zone, which is unsaturated during low river stage.« less

Chromium carcinogenicity: California strategies.

PubMed

Alexeeff, G V; Satin, K; Painter, P; Zeise, L; Popejoy, C; Murchison, G

1989-10-01

Hexavalent chromium was identified by California as a toxic air contaminant (TAC) in January 1986. The California Department of Health Services (CDHS) concurred with the findings of the International Agency for Research on Cancer that there is sufficient evidence to demonstrate the carcinogenicity of chromium in both animals and humans. CDHS did not find any compelling evidence demonstrating the existence of a threshold with respect to chromium carcinogenesis. Experimental data was judged inadequate to assess potential human reproductive risks from ambient exposures. Other health effects were not expected to occur at ambient levels. The theoretically increased lifetime carcinogenic risk from a continuous lifetime exposure to hexavalent chromium fell within the range 12-146 cancer cases per nanogram hexavalent chromium per cubic meter of air per million people exposed, depending on the potency estimate used. The primary sources found to contribute significantly to the risk of exposure were chrome platers, chromic acid anodizing facilities and cooling towers utilizing hexavalent chromium as a corrosion inhibitor. Evaluation of genotoxicity data, animal studies and epidemiological studies indicates that further consideration should be given to the potential carcinogenicity of hexavalent chromium via the oral route.

Biosorption and biotransformation of hexavalent chromium [Cr(VI)]: A comprehensive review.

PubMed

Jobby, Renitta; Jha, Pamela; Yadav, Anoop Kumar; Desai, Nitin

2018-05-09

Chromium (VI) is one of the most common environmental contaminant due to its tremendous industrial applications. It is non-biodegradable as it is a heavy metal, and hence, of major concern. Therefore, it is pertinent that the remediation method should be such that brings chromium within permissible limits before the effluent is discharged. Several different strategies are adopted by microorganisms for Cr (VI) removal mostly involving biosorption and biotransformation or both. These mechanisms are based on the surface nature of the biosorbent and the availability of reductants. This review article focuses on chromium pollution problem, its chemistry, sources, effects, remediation strategies by biological agents and detailed chromium detoxification mechanism in microbial cell. A summary of applied in situ and ex situ chromium bioremediation technologies is also listed. This can be helpful for developing technologies to be more efficient for Cr (VI) removal thereby bridging the gap between laboratory findings and industrial application for chromium remediation. Copyright © 2018 Elsevier Ltd. All rights reserved.

Efficacy of dietary chromium (III) supplementation on tissue chromium deposition in finishing pigs.

PubMed

Wang, Min-Qi; Li, Hui; He, Yu-Dan; Wang, Chao; Tao, Wen-Jing; Du, Yong-Jie

2012-09-01

The study was conducted to evaluate the efficacy of different forms of trivalent chromium (Cr) supplementation on tissue chromium deposition in finishing pigs. A total of 96 pigs with an initial average body mass 65.57±1.05 kg were blocked by body mass and randomly assigned to four treatments with three replicates. Pigs were offered one of four diets including a control diet or the control diet supplemented with 200 μg/kg chromium from either chromium chloride (CrCl(3)), chromium picolinate (CrPic) or chromium nanocomposite (CrNano) for 40 days. During the trial, all pigs were given free access to feed and water. After feeding trial, eight pigs from each treatment were slaughtered for samples collection. The results showed that supplemental CrNano increased Cr content in blood, longissimus muscle, heart, liver, kidney, jejunum, and ileum (P<0.05). Supplemental Cr from three sources increased Cr excretion from all feces (P<0.05). Urinary Cr excretion was increased by CrNano or CrPic supplementation significantly. These results suggested that chromium nanocomposite exhibited more effective on tissue Cr deposition in pigs, which indicated higher absorption compared with CrCl(3) and CrPic.

Chromium recovery from exhausted baths generated in plating processes and its reuse in the tanning industry.

PubMed

Torras, Josep; Buj, Irene; Rovira, Miquel; de Pablo, Joan

2012-03-30

Chromium plating used for functional purposes provides an extremely hard, wear and corrosion resistant layer by means of electrolytic deposition. Typical layer thicknesses range between 2.5 and 500 μm. Chromium electroplating baths contain high concentrations of Cr(VI) with chromium trioxide (CrO(3)) as the chromium source. When because of technical or economic reasons a bath gets exhausted, a waste containing mainly chromium as dichromate as well as other heavy metals is generated. Chromium may then be purified for use in other industrial processes with different requirements. In this work, a sustainable system for using galvanic wastes as reagents in the leather tanning industry, thus reducing quantity of wastes to be treated, is presented. Metal cations present in the chromium exhausted bath were precipitated with NaOH. Then, the solution containing mainly soluble Cr(VI) was separated. By means of sodium sulphite in acidic conditions, Cr(VI) was reduced to Cr(III) as chromium (III) sulphate. From chromium (III) sulphate a basic Cr(III) sulphate may be obtained, which is one of most used compounds in the tanning industry. Cr(III) concentration in the final solution allows its reuse without concentration, but with a slight dilution. Copyright © 2012 Elsevier B.V. All rights reserved.

Health Assessment Document for Chromium (Final Report, 1983)

EPA Science Inventory

This final report summarizes a comprehensive database that considers all sources of chromium in the environment, the likelihood for its exposure to humans, and the possible consequences to man and lower organisms from its absorption. This information is integrated into a format t...

Review of occupational epidemiology of chromium chemicals and respiratory cancer.

PubMed

Hayes, R B

1988-06-01

Several epidemiologic studies have investigated the association between cancer risk and employment in chromium producing and using industries. Strong and consistent associations have been found between employment in the primary chemical producing industry and the risk for respiratory cancer. Workers employed in chromate pigment production and possibly spray painters of chromate pigment paints appear to be at excess risk of respiratory cancer. Chrome platers may also be at excess risk, although the evidence is limited. A few studies indicate that chromium alloy welding may also be an exposure source of concern. Some studies of ferrochromium alloy workers have shown an excess risk for respiratory cancer, although the risk may in part be due to concomitant exposures. The evidence indicates that the hexavalent form of chromium is the primary agent of chromium carcinogenesis. Solubility and other characteristics of chromium compounds may also play a role in determining risk.

Analysis of chromium status in the revegetated flora of a tannery waste site and microcosm studies using earthworm E. fetida.

PubMed

Nirola, Ramkrishna; Megharaj, Mallavarapu; Subramanian, Avudainayagam; Thavamani, Palanisami; Ramadass, Kavitha; Aryal, Rupak; Saint, Christopher

2018-02-01

Chromium from tannery waste dump site causes significant environmental pollution affecting surrounding flora and fauna. The primary aims of this study were to survey vegetation, investigate the degree of soil pollution occurring near tannery waste dump site and make a systematic evaluation of soil contamination based on the chromium levels found in plants and earthworms from the impacted areas. This paper presents the pollution load of toxic heavy metals, and especially chromium, in 10 soil samples and 12 species of plants. Soil samples were analysed for heavy metals by using ICP-MS/ICP-OES method. Results indicated that Cr in soils exceeded soil quality guideline limits (SQGL). The total chromium present in the above ground parts of plants ranged from 1.7 mg kg -1 in Casuarina sp. to 1007 mg kg -1 in Sonchus asper. The Cr bioaccumulation in Eisenia fetida from tannery waste soil ranged from 5 to 194 mg kg -1 . The high enrichment factor of Cr in S. asper and bioaccumulation factor in earthworms indicate that there is a steady increase of toxic chromium risk in this area, which could be correlated with the past dumping activity. Emphasis needs to be put on control measures of pollution and remediation techniques in such areas to achieve an ecologically sustainable industrialisation.

SUMMARY CONCLUSIONS FOR THE PILOT IN-SITU CHROMIUM REDUCTION TEST AT RIVERBANK ARMY AMMUNITIONS PLANT

DOE Office of Scientific and Technical Information (OSTI.GOV)

Ridley, M

2007-04-25

A treatability study was conducted at Riverbank Army Ammunition Plant's (RBAAP) Site 17, to evaluate the effectiveness of a permeable reactive barrier (PRB) for the treatment of hexavalent chromium (Cr{sup 6+}). The chromium contamination at Site 17 is hydrologically isolated and unsuitable for standard extraction and treatment (pump and treat). The majority of the chromium contamination at Site 17 is trapped within the fine grain sediments of a clay/slit zone (45 to 63). The PRB was established above and adjacent to the contaminated zone at Site 17 to reduce the hexavalent chromium as it leaches out of the contaminated clay/siltmore » zone separating the A zone from the A zone. Site 17 and the monitoring network are described in the In-Situ Chromium Reduction Treatability Study Work Plan (CH2MHILL, January 2004). The PRB was created by reducing naturally occurring Fe{sup 3+} to Fe{sup 2+} with the injection of a buffered sodium dithionite solution into subsurface chromium source area. The Cr{sup 6+} leaching out of the contaminated clay/silt zone and migrating through the PRB is reduced by Fe{sup 2+} to Cr{sup 3+} and immobilized (Amonette, et al., 1994). The sodium dithionite will also reduce accessible Cr{sup 6+}, however the long-term reductant is the Fe{sup 2+}. Bench scale tests (Appendix A) were conducted to assess the quantity and availability of the naturally occurring iron at Site 17, the ability of the sodium dithionite to reduce the hexavalent chromium and Fe within the sediments, and the by-products produced during the treatment. Appendix A, provides a detailed description of the laboratory treatability tests, and provides background information on the technologies considered as possible treatment options for Site 17. Following the sodium dithionite treatment, groundwater/treatment solution was extracted to remove treatment by-products (sulfate, manganese, and iron). The following sections briefly discuss the current treatment status, future recommendations for Site 17, and future recommendations for the application of sodium dithionite at additional sites. At the completion of the treatability test, none of the wells at Site 17 had detectable hexavalent chromium, but the sulfate, iron, and manganese concentrations were detected and exceeded the CA secondary drinking water standards. The extraction done after the injection of the sodium dithionite solution to remove the sulfate, manganese, and iron has to a large extent negated the effectiveness of the iron reduction. Riverbank's local groundwater is naturally high in dissolved oxygen (concentration range at Site 17: 1.8 to 6.0 mg/l) and moving this type of groundwater through the reduced zone caused oxidation of the Fe2+ within the treatment zone, followed by a new release of hexavalent chromium detected in one of the treatment wells. Additional extraction at Site 17 will continue to degrade the PRB, threatening to release additional Cr{sup 6+} into the groundwater. Sulfate and manganese only exceed the CA secondary drinking water standards in the area immediately surrounding the PRB. It is unlikely that these contaminants will threaten any water supply wells in the area. The chromium concentrations are increasing in IW-17. The current concentration is still only a third of the original concentration. It might be worth investigating some of the new zero valent iron treatments, such as nanoscale zero-valent iron (NZVI) to replace the in-situ naturally occurring iron, which may no longer be available for reduction. The NZVI has been successfully tested at NASA in Florida (O'Hara, 2006), and demonstrated no release of metals from the natural sediments. This might also be a viable option for other sites at RBAAP.« less

Nutritional assessment of processing effects on major and trace element content in sea buckthorn juice (Hippophaë rhamnoides L. ssp. rhamnoides).

PubMed

Gutzeit, D; Winterhalter, P; Jerz, G

2008-08-01

Processing effects on the mineral content were investigated during juice production from sea buckthorn (Hippophaë rhamnoides L. ssp. rhamnoides, Elaeagnaceae) using berries from 2 different growing areas. The major and trace elements of sea buckthorn berries and juices were determined by atomic absorption spectroscopy (AAS)--(calcium, iron, magnesium, potassium, sodium) and inductively coupled plasma-mass spectrometry (ICP-MS)--(arsenic, boron, chromium, copper, manganese, molybdenum, nickel, selenium, zinc). Potassium is the most abundant major element in sea buckthorn berries and juices. The production process increased the potassium content in the juice by about 20%. Moreover, the processing of juice increased the value of manganese up to 32% compared to the content in berries. During industrial juice production, the technological steps caused a loss of about 53% to 77% of the chromium concentration, 50% of the copper content, 64% to 75% of the molybdenum amount, and up to 45% of the iron concentration in the final juice product. Consumption of sea buckthorn juice represents a beneficial source of chromium, copper, manganese, molybdenum, iron, and potassium for the achievement of the respective dietary requirements.

40 CFR 468.13 - New source performance standards (NSPS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... rolled Chromium 0.038 0.015 Copper 0.131 0.062 Lead 0.010 0.0092 Nickel 0.056 0.038 Zinc 0.105 0.043 Oil... per 1,000,000 off-pounds of copper or copper alloy cold rolled Chromium 0.140 0.056 Copper 0.485 0.231... drawn Chromium 0.031 0.012 Copper 0.108 0.051 Lead 0.0085 0.0076 Nickel 0.046 0.031 Zinc 0.086 0.035 Oil...

40 CFR 461.74 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2011 CFR

2011-07-01

... of zinc Chromium 0.24 0.099 Mercury 0.14 0.055 Silver 0.23 0.093 Zinc 0.80 0.34 Manganese 0.37 0.16... Chromium 0.030 0.12 Mercury 0.017 0.006 Silver 0.028 0.012 Zinc 0.099 0.042 Manganese 0.046 0.020 (3... monthly average Metric units—mg/kg of zinc English units—pounds per 1,000,000 pounds of zinc Chromium 9.53...

Carcinogenicity and mutagenicity of chromium.

PubMed

Léonard, A; Lauwerys, R R

1980-11-01

Occupational exposure represents the main source of human contamination by chromium. For non-occupationally exposed people the major environmental exposure to chromium occurs as a consequence of its presence in food. Chromium must be considered as an essential element. Its deficiency impairs glucose metabolism. Trivalent chromium salts are poorly absorbed through the gastro-intestinal and respiratory tracts because they do not cross membranes easily. Hexavalent chromium can be absorbed by the oral and pulmonary routes and probably also through the skin. After its absorption, hexavalent chromium is rapidly reduced to the trivalent form which is probably the only form to be found in biological material. Epidemiological studies have shown that some chromium salts (mainly the slightly soluble hexavalent salts) are carcinogens. Lung cancers have, indeed, often been reported among workers in chromate-producing industry and, to a lesser extent, in workers from the chrome-pigment industry. The first attempts to produce cancers in experimental animals by inhalation or parenteral introduction gave negative or equivocal results but, from 1960, positive results have been obtained with various chromium compounds. As for the carcinogenic activity, the mutagenicity of chromium has mainly been found with hexavalent salts. In the majority of assay systems used, trivalent chromium appears inactive. It can be considered as evident, however, that the ultimate mutagen which binds to the genetic material is the trivalent form produced intracellularly from hexavalent chromium, the apparent lack of activity of the trivalent form being due to its poor cellular uptake.

Performance Assessment of a Permeable Reactive Barrier for Ground Water Remediation Fifteen Years After Installation

EPA Science Inventory

The fifteen-year performance of a granular iron, permeable reactive barrier (PRB; Elizabeth City, North Carolina) is reviewed with respect to contaminanttreatment (hexavalent chromium and trichloroethylene) and hydraulic performance. Due to in-situ treatment of the chromium sourc...

Direct determination of chromium in infant formulas employing high-resolution continuum source electrothermal atomic absorption spectrometry and solid sample analysis.

PubMed

Silva, Arlene S; Brandao, Geovani C; Matos, Geraldo D; Ferreira, Sergio L C

2015-11-01

The present work proposed an analytical method for the direct determination of chromium in infant formulas employing the high-resolution continuum source electrothermal atomic absorption spectrometry combined with the solid sample analysis (SS-HR-CS ET AAS). Sample masses up to 2.0mg were directly weighted on a solid sampling platform and introduced into the graphite tube. In order to minimize the formation of carbonaceous residues and to improve the contact of the modifier solution with the solid sample, a volume of 10 µL of a solution containing 6% (v/v) H2O2, 20% (v/v) ethanol and 1% (v/v) HNO3 was added. The pyrolysis and atomization temperatures established were 1600 and 2400 °C, respectively, using magnesium as chemical modifier. The calibration technique was evaluated by comparing the slopes of calibration curves established using aqueous and solid standards. This test revealed that chromium can be determined employing the external calibration technique using aqueous standards. Under these conditions, the method developed allows the direct determination of chromium with limit of quantification of 11.5 ng g(-1), precision expressed as relative standard deviation (RSD) in the range of 4.0-17.9% (n=3) and a characteristic mass of 1.2 pg of chromium. The accuracy was confirmed by analysis of a certified reference material of tomato leaves furnished by National Institute of Standards and Technology. The method proposed was applied for the determination of chromium in five different infant formula samples. The chromium content found varied in the range of 33.9-58.1 ng g(-1) (n=3). These samples were also analyzed employing ICP-MS. A statistical test demonstrated that there is no significant difference between the results found by two methods. The chromium concentrations achieved are lower than the maximum limit permissible for chromium in foods by Brazilian Legislation. Copyright © 2015. Published by Elsevier B.V.

Cr(VI) Occurrence and Geochemistry in Water From Public-Supply Wells in California

DOE PAGES

Izbicki, John A.; Wright, Michael T.; Seymour, Whitney A.; ...

2015-08-18

Hexavalent chromium, Cr(VI), in 918 wells sampled throughout California between 2004 and 2012 by the Groundwater Ambient Monitoring and Assessment Program—Priority Basin Project (GAMA—PBP) ranged from less than the study reporting limit (SRL) of 1 microgram per liter (μg/L) to 32 μg/L. Statewide, Cr(VI) was reported in 31 percent of sampled wells and equaled or exceeded the recently established (2014) California Maximum Contaminant Level (MCL) for Cr(VI) of 10 μg/L in 4 percent of sampled wells. Cr(VI) data collected for regulatory purposes overestimate Cr(VI) occurrence. Ninety percent of chromium was present as Cr(VI), which was detected more frequently and atmore » higher concentrations in alkaline (pH > 8), oxic water, and more frequently in agricultural and urban land uses compared to native land uses. Chemical, isotopic (tritium and carbon-14), and noble-gas data show high Cr(VI) in water from wells in alluvial aquifers in the southern California deserts result from long groundwater-residence times and geochemical reactions such as silicate weathering that increase pH, while oxic conditions persist. High Cr(VI) in water from wells in alluvial aquifers along the west-side of the Central Valley results from high-chromium abundance in source rock eroded to form those aquifers, and areal recharge processes (including irrigation return) that mobilize chromium from the unsaturated zone. Cr(VI) co-occurred with oxyanions having similar chemistry, including vanadium, selenium, and uranium. Cr(VI) was positively correlated with nitrate, consistent with increased concentrations in areas of agricultural land use and mobilization of chromium from the unsaturated zone by irrigation return.« less

Cr(VI) occurrence and geochemistry in water from public-supply wells in California

USGS Publications Warehouse

Izbicki, John; Wright, Michael; Seymour, Whitney A.; McCleskey, R. Blaine; Fram, Miranda S.; Belitz, Kenneth; Esser, Bradley K.

2015-01-01

Hexavalent chromium, Cr(VI), in 918 wells sampled throughout California between 2004 and 2012 by the Groundwater Ambient Monitoring and Assessment-Priority Basin Project (GAMA-PBP) ranged from less than the study reporting limit of 1 microgram per liter (μg/L) to 32 μg/L. Statewide, Cr(VI) was reported in 31 percent of wells and equaled or exceeded the recently established (2014) California Maximum Contaminant Level (MCL) for Cr(VI) of 10 μg/L in 4 percent of wells. Cr(VI) data collected for regulatory purposes overestimated Cr(VI) occurrence compared to spatially-distributed GAMA-PBP data. Ninety percent of chromium was present as Cr(VI), which was detected more frequently and at higher concentrations in alkaline (pH ≥ 8), oxic water; and more frequently in agricultural and urban land uses compared to native land uses. Chemical, isotopic (tritium and carbon-14), and noble-gas data show high Cr(VI) in water from wells in alluvial aquifers in the southern California deserts result from long groundwater-residence times and geochemical reactions such as silicate weathering that increase pH, while oxic conditions persist. High Cr(VI) in water from wells in alluvial aquifers along the west-side of the Central Valley results from high-chromium in source rock eroded to form those aquifers, and areal recharge processes (including irrigation return) that can mobilize chromium from the unsaturated zone. Cr(VI) co-occurred with oxyanions having similar chemistry, including vanadium, selenium, and uranium. Cr(VI) was positively correlated with nitrate, consistent with increased concentrations in areas of agricultural land use and mobilization of chromium from the unsaturated zone by irrigation return.

Progress in the chemistry of chromium(V) doping agents used in polarized target materials

DOE Office of Scientific and Technical Information (OSTI.GOV)

Krumpolc, M.; Hill, D.; Struhrmann, H.B.

1990-01-01

We wish to report progress in two areas of the chromium (V)-based doping agents: Two commonly used chromium (V) complexes, I and II, have been synthesized in perdeuterated form (i.e., all hydrogens replaced by deuterium). They are sodium bis(2-ethyl-2-deuteroxy-butyrato)oxochromate(V)monodeuterate, IV, (acronym EDBA-Cr(V)), and sodium bis(2-deuteroxy-2-methylpropionato)oxochromate(V), III, (acronym DMPA-Cr(V)). A synthetic route leading to the preparation of stable, chromium(III)-free solutions of chromium(V) in diols (1,2-ethanediol/ethylene glycol/and 1,2-propanediol/propylene glycol/) has been outlined.

21 CFR 73.2327 - Chromium oxide greens.

Code of Federal Regulations, 2014 CFR

2014-04-01

... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2327 Chromium oxide greens. (a) Identity and... may be safely used in externally applied cosmetics, including cosmetics intended for use in the area...

21 CFR 73.2327 - Chromium oxide greens.

Code of Federal Regulations, 2012 CFR

2012-04-01

... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2327 Chromium oxide greens. (a) Identity and... may be safely used in externally applied cosmetics, including cosmetics intended for use in the area...

21 CFR 73.2327 - Chromium oxide greens.

Code of Federal Regulations, 2013 CFR

2013-04-01

... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2327 Chromium oxide greens. (a) Identity and... may be safely used in externally applied cosmetics, including cosmetics intended for use in the area...

40 CFR 63.401 - Definitions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... subpart are defined in the Act, in subpart A of this part, or in this section as follows: Chromium-based water treatment chemicals means any combination of chemical substances containing chromium used to treat... operational limitation on the capacity of the stationary source to emit a pollutant, including air pollution...

Removal of elevated level of chromium in groundwater by the fabricated PANI/Fe3O4 nanocomposites.

PubMed

Ramachandran, Aruna; Prasankumar, T; Sivaprakash, S; Wiston, Biny R; Biradar, Santhosh; Jose, Sujin

2017-03-01

In this work, we report the reduction of chromium concentration in the polluted groundwater samples from Madurai Kamaraj University area, India, where the dissolved salts in groundwater are reported as serious health hazards for its inhabitants. The water samples have intolerable amounts of total dissolved solids (TDS) and chromium is a prominent pollutant among them. Chromium reduction was achieved by treating the polluted groundwater with PANI/Fe 3 O 4 nanocomposites synthesized by in situ polymerization method. Further experimentation showed that the nanocomposites exhibit better chromium removal characteristics upon increasing the aniline concentration during the synthesis. We were able to reduce chromium concentration in the samples from 0.295 mg L -1 to a tolerable amount of 0.144 mg L -1 . This work is expected to open doors for chromium-free groundwater in various regions of India, when improved to an industrial scale.

40 CFR 461.74 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2012 CFR

2012-07-01

...,000 pounds of zinc Chromium 0.24 0.099 Mercury 0.14 0.055 Silver 0.23 0.093 Zinc 0.80 0.34 Manganese 0... of zinc Chromium 0.030 0.12 Mercury 0.017 0.006 Silver 0.028 0.012 Zinc 0.099 0.042 Manganese 0.046 0... Chromium 9.53 3.90 Mercury 5.42 2.17 Silver 8.89 3.68 Zinc 31.64 13.22 Manganese 14.74 6.28 (4) Subpart G...

40 CFR 461.74 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2013 CFR

2013-07-01

...,000 pounds of zinc Chromium 0.24 0.099 Mercury 0.14 0.055 Silver 0.23 0.093 Zinc 0.80 0.34 Manganese 0... of zinc Chromium 0.030 0.12 Mercury 0.017 0.006 Silver 0.028 0.012 Zinc 0.099 0.042 Manganese 0.046 0... Chromium 9.53 3.90 Mercury 5.42 2.17 Silver 8.89 3.68 Zinc 31.64 13.22 Manganese 14.74 6.28 (4) Subpart G...

40 CFR 461.74 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2014 CFR

2014-07-01

...,000 pounds of zinc Chromium 0.24 0.099 Mercury 0.14 0.055 Silver 0.23 0.093 Zinc 0.80 0.34 Manganese 0... of zinc Chromium 0.030 0.12 Mercury 0.017 0.006 Silver 0.028 0.012 Zinc 0.099 0.042 Manganese 0.046 0... Chromium 9.53 3.90 Mercury 5.42 2.17 Silver 8.89 3.68 Zinc 31.64 13.22 Manganese 14.74 6.28 (4) Subpart G...

Basewide Groundwater Operable Unit. Groundwater Operable Unit Remedial Investigation/Feasibility Study Report. Volume 2

DTIC Science & Technology

1994-06-01

Boron -- - .- Cadmium (3.9) (1.1) 1.4a,c 0 .55a.b Chromium , Hexavalent (16) lid _______ Chromium , Trivalent 1,700 21016li Cobalt -- -- .- Copper (18...same time period as those for VOCs should be used, if possible. Response: Four figures have been prepared showing the lead, nickel, chromium , manganese...equipment proposed at the GWTP, and the only NSPS source category that might be considered applicable to the existing thermal fume incinerator is Subpart E

40 CFR 468.15 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2014 CFR

2014-07-01

...—pounds per 1,000,000 off-pounds of copper or copper alloy hot rolled Chromium 0.038 0.015 Copper 0.131 0... Chromium 0.140 0.056 Copper 0.485 0.231 Lead 0.037 0.034 Nickel 0.208 0.140 Zinc 0.386 0.159 TTO 0.128 0... copper alloy drawn Chromium 0.031 0.012 Copper 0.108 0.051 Lead 0.0085 0.0076 Nickel 0.046 0.031 Zinc 0...

40 CFR 468.15 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2013 CFR

2013-07-01

...—pounds per 1,000,000 off-pounds of copper or copper alloy hot rolled Chromium 0.038 0.015 Copper 0.131 0... Chromium 0.140 0.056 Copper 0.485 0.231 Lead 0.037 0.034 Nickel 0.208 0.140 Zinc 0.386 0.159 TTO 0.128 0... copper alloy drawn Chromium 0.031 0.012 Copper 0.108 0.051 Lead 0.0085 0.0076 Nickel 0.046 0.031 Zinc 0...

40 CFR 468.15 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2012 CFR

2012-07-01

...—pounds per 1,000,000 off-pounds of copper or copper alloy hot rolled Chromium 0.038 0.015 Copper 0.131 0... Chromium 0.140 0.056 Copper 0.485 0.231 Lead 0.037 0.034 Nickel 0.208 0.140 Zinc 0.386 0.159 TTO 0.128 0... copper alloy drawn Chromium 0.031 0.012 Copper 0.108 0.051 Lead 0.0085 0.0076 Nickel 0.046 0.031 Zinc 0...

21 CFR 73.2326 - Chromium hydroxide green.

Code of Federal Regulations, 2013 CFR

2013-04-01

... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2326 Chromium hydroxide green. (a) Identity and... in coloring externally applied cosmetics, including those intended for use in the area of the eye, in...

21 CFR 73.2326 - Chromium hydroxide green.

Code of Federal Regulations, 2014 CFR

2014-04-01

... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2326 Chromium hydroxide green. (a) Identity and... in coloring externally applied cosmetics, including those intended for use in the area of the eye, in...

21 CFR 73.2326 - Chromium hydroxide green.

Code of Federal Regulations, 2012 CFR

2012-04-01

... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2326 Chromium hydroxide green. (a) Identity and... in coloring externally applied cosmetics, including those intended for use in the area of the eye, in...

Processes affecting the remediation of chromium-contaminated sites.

PubMed

Palmer, C D; Wittbrodt, P R

1991-05-01

The remediation of chromium-contaminated sites requires knowledge of the processes that control the migration and transformation of chromium. Advection, dispersion, and diffusion are physical processes affecting the rate at which contaminants can migrate in the subsurface. Heterogeneity is an important factor that affects the contribution of each of these mechanisms to the migration of chromium-laden waters. Redox reactions, chemical speciation, adsorption/desorption phenomena, and precipitation/dissolution reactions control the transformation and mobility of chromium. The reduction of CrVI to CrIII can occur in the presence of ferrous iron in solution or in mineral phases, reduced sulfur compounds, or soil organic matter. At neutral to alkaline pH, the CrIII precipitates as amorphous hydroxides or forms complexes with organic matter. CrIII is oxidized by manganese dioxide, a common mineral found in many soils. Solid-phase precipitates of hexavalent chromium such as barium chromate can serve either as sources or sinks for CrVI. Adsorption of CrVI in soils increases with decreasing chromium concentration, making it more difficult to remove the chromium as the concentration decreases during pump-and-treat remediation. Knowledge of these chemical and physical processes is important in developing and selecting effective, cost-efficient remediation designs for chromium-contaminated sites.

An Investigation of Technologies for Hazardous Sludge Reduction at AFLC (Air Force Logistics Command) Industrial Waste Treatment Plants. Volume 2. Literature Review of Available Technologies for Treating Heavy Metal Wastewaters.

DTIC Science & Technology

1983-12-01

plate quality. Dummying of chromium baths is used in the special case where high cathode-to-anode 15ea ratio has resulted in build up of trivalent ... chromium (Cr ).Dummying with a high anode -to-cat hode area ratio can be used to reoxidize the trivalent to hexavalent chromium (Cr +6 ). Proper...the trivalent state, which then can be precipitated as chromium hydroxide by alkali neutralization " Cyanide oxidation (if needed) of segregated

Spatial distribution variation and probabilistic risk assessment of exposure to chromium in ground water supplies; a case study in the east of Iran.

PubMed

Fallahzadeh, Reza Ali; Khosravi, Rasoul; Dehdashti, Bahare; Ghahramani, Esmail; Omidi, Fariborz; Adli, Abolfazl; Miri, Mohammad

2018-05-01

A high concentration of chromium (VI) in groundwater can threaten the health of consumers. In this study, the concentration of chromium (VI) in 18 drinking water wells in Birjand, Iran, s was investigated over a period of two yearsNon-carcinogenic risk assessment, sensitivity, and uncertainty analysis as well as the most important variables in determining the non-carcinogenic risk for three age groups including children, teens, and adults, were performed using the Monte Carlo simulations technique. The northern and southern regions of the study area had the highest and lowest chromium concentrations, respectively. The chromium concentrations in 16.66% of the samples in an area of 604.79 km2 were more than World Health Organization (WHO) guideline (0.05 mg/L). The Moran's index analysis showed that the distribution of contamination is a cluster. The Hazard Index (HI) values for the children and teens groups were 1.02 and 2.02, respectively, which was more than 1. A sensitivity analysis indicated that the most important factor in calculating the HQ was the concentration of chromium in the consumed water. HQ values higher than 1 represent a high risk for the children group, which should be controlled by removing the chromium concentration of the drinking water. Copyright © 2018 Elsevier Ltd. All rights reserved.

REDUCTIVE DETOXIFICATION AND IMMOBILIZATION OF CHROMATE PRESENT IN SOILS

EPA Science Inventory

Sodium dithionite was used to treat a chromium source zone in soils beneath an old chrome plating shop. The sodium dithionite was injected as a buffered solution into the soils to transform the chromium from the oxidized (+6) state to the reduced (+3) state. Once reduced the chro...

Release of Hexavalent Chromium by Ash and Soils in Wildfire-Impacted Areas

USGS Publications Warehouse

Wolf, Ruth E.; Morman, Suzette A.; Plumlee, Geoffrey S.; Hageman, Philip L.; Adams, Monique

2008-01-01

The highly oxidizing environment of a wildfire has the potential to convert any chromium present in the soil or in residential or industrial debris to its more toxic form, hexavalent chromium, a known carcinogen. In addition, the highly basic conditions resulting from the combustion of wood and wood products could result in the stabilization of any aqueous hexavalent chromium formed. Samples were collected from the October 2007 wildfires in Southern California and subjected to an array of test procedures to evaluate the potential effects of fire-impacted soils and ashes on human and environmental health. Soil and ash samples were leached using de-ionized water to simulate conditions resulting from rainfall on fire-impacted areas. The resulting leachates were of high pH (10-13) and many, particularly those of ash from burned residential areas, contained elevated total chromium as much as 33 micrograms per liter. Samples were also leached using a near-neutral pH simulated lung fluid to model potential chemical interactions of inhaled particles with fluids lining the respiratory tract. High Performance Liquid Chromatography coupled to Inductively Coupled Plasma Mass Spectrometry was used to separate and detect individual species (for example, Cr+3, Cr+6, As+3, As+5, Se+4, and Se+6). These procedures were used to determine the form of the chromium present in the de-ionized water and simulated lung fluid leachates. The results show that in the de-ionized water leachate, all of the chromium present is in the form of Cr+6, and the resulting high pH tends to stabilize Cr+6 from reduction to Cr+3. Analysis of the simulated lung fluid leachates indicates that the predominant form of chromium present in the near-neutral pH of lung fluid would be Cr+6, which is of concern due to the high possibility of inhalation of the small ash and soil particulates, particularly by fire or restoration crews.

An integrated approach to assess heavy metal source apportionment in peri-urban agricultural soils.

PubMed

Huang, Ying; Li, Tingqiang; Wu, Chengxian; He, Zhenli; Japenga, Jan; Deng, Meihua; Yang, Xiaoe

2015-12-15

Three techniques (Isotope Ratio Analysis, GIS mapping, and Multivariate Statistical Analysis) were integrated to assess heavy metal pollution and source apportionment in peri-urban agricultural soils. The soils in the study area were moderately polluted with cadmium (Cd) and mercury (Hg), lightly polluted with lead (Pb), and chromium (Cr). GIS Mapping suggested Cd pollution originates from point sources, whereas Hg, Pb, Cr could be traced back to both point and non-point sources. Principal component analysis (PCA) indicated aluminum (Al), manganese (Mn), nickel (Ni) were mainly inherited from natural sources, while Hg, Pb, and Cd were associated with two different kinds of anthropogenic sources. Cluster analysis (CA) further identified fertilizers, waste water, industrial solid wastes, road dust, and atmospheric deposition as potential sources. Based on isotope ratio analysis (IRA) organic fertilizers and road dusts accounted for 74-100% and 0-24% of the total Hg input, while road dusts and solid wastes contributed for 0-80% and 19-100% of the Pb input. This study provides a reliable approach for heavy metal source apportionment in this particular peri-urban area, with a clear potential for future application in other regions. Copyright © 2015 Elsevier B.V. All rights reserved.

Hexavalent chromium monitor

DOEpatents

Tao, Shiquan; Winstead, Christopher B.

2005-04-12

A monitor is provided for use in measuring the concentration of hexavalent chromium in a liquid, such as water. The monitor includes a sample cell, a light source, and a photodetector. The sample cell is in the form of a liquid-core waveguide, the sample cell defining an interior core and acting as a receiver for the liquid to be analyzed, the interior surface of the sample cell having a refractive index of less than 1.33. The light source is in communication with a first end of the sample cell for emitting radiation having a wavelength of about and between 350 to 390 nm into the interior core of the waveguide. The photodetector is in communication with a second end of the waveguide for measuring the absorption of the radiation emitted by the light source by the liquid in the sample cell. The monitor may also include a processor electronically coupled to the photodetector for receipt of an absorption signal to determine the concentration of hexavalent chromium in the liquid.

Chemical contamination and physical characteristics of sediments in the upper Great Lakes connecting channels 1985

USGS Publications Warehouse

Bertram, Paul E.; Edsall, Thomas A.; Manny, Bruce A.; Nichols, Susan J.; Schloesser, Donald W.

1991-01-01

Contamination of sediments by toxic organic substances and heavy metals was widespread throughout the connecting channels of the upper Great Lakes in 1985. Sediments at 250 stations in the connecting channels were analyzed for total PCBs, oil and grease, phenols, total cyanide, total volatile solids, mercury, cadmium, chromium, cobalt, copper, lead, nickel, and zinc, and the results were evaluated according to U.S. EPA guidelines for polluted sediments. Sediments were most heavily contaminated near industrialized areas, although some areas more than 40 km downstream from known point sources of pollution were moderately contaminated by oil and metals.

IMPACT OF LEATHER PROCESSING INDUSTRIES ON CHROMIUM CONCENTRATION IN GROUNDWATER SOUTH OF CHENNAI CITY, INDIA

NASA Astrophysics Data System (ADS)

Elango, L.; Brindha, K.; G. Rajesh, V.

2009-12-01

The groundwater quality is under threat due to disposal of effluents from a number of industries. Poor practice of treatment of wastes from tanning industries or leather processing industries lead to pollution of groundwater. This study was carried out with the objective of assessing the impact of tanneries on groundwater quality in Chromepet area which is a part of the metropolitan area of Chennai, Tamil Nadu, India. This area serves as the home town for a number of small and large scale tanning industries. People in certain parts of this area depend on the groundwater for their domestic needs as there is no piped drinking water supply system. Topographically this region is generally flat with gentle slope towards east and north east. The charnockite rocks occur as basement at the depth of about 15m from the surface of this area. Weathered charnockite rock occurs at the depth from 7m to 15m from the ground surface. The upper layer consists of loamy soil. Groundwater occurs in the unconfined condition at a depth from 0.5m to 5m. Thirty six groundwater samples were collected during March 2008 and the groundwater samples were analysed for their heavy metal (chromium) content using atomic absorption spectrophotometer. Bureau of Indian Standards (BIS) recommended the maximum permissible limit of chromium in drinking water as 0.05 mg/l. Considering this, it was found that 86% of the groundwater samples possessed concentration of chromium above the maximum permissible limit recommended by BIS. The tanneries use chrome sulphate to strengthen the leather and make it water repellent. The excess of chromium gets washed off and remains in the wastewater. This wastewater is disposed into open uncovered drains either untreated or after partial treatment. Thus the chromium leaches through the soil and reaches the groundwater table. Apart from this, there is also huge quantity of solid waste resulting from the hides and skins which are dumped off without suitable treatment. The percolation of the leachate rich in chromium will also add to chromium concentration in groundwater. The effluents from the tanning processes are sent to the common effluent treatment plant (CETP) by large scale industries. But small scale industries are not able to use such CETP for treating the wastewater generated by them. It is prominent from this study that the effluent from the tanning industries should be treated properly before disposing off into drains in order to prevent the pollution of groundwater. Reverse osmosis treatment of tanning effluent can be adopted for separation and recovery of chromium from the wastewater. For improving the already contaminated groundwater of this region, insitu bioremediation by the use of microorganisms isolated from the contaminated site will prove effective.

Recent Advances in On-Line Methods Based on Extraction for Speciation Analysis of Chromium in Environmental Matrices.

PubMed

Trzonkowska, Laura; Leśniewska, Barbara; Godlewska-Żyłkiewicz, Beata

2016-07-03

The biological activity of Cr(III) and Cr(VI) species, their chemical behavior, and toxic effects are dissimilar. The speciation analysis of Cr(III) and Cr(VI) in environmental matrices is then of great importance and much research has been devoted to this area. This review presents recent developments in on-line speciation analysis of chromium in such samples. Flow systems have proved to be excellent tools for automation of sample pretreatment, separation/preconcentration of chromium species, and their detection by various instrumental techniques. Analytical strategies used in chromium speciation analysis discussed in this review are divided into categories based on selective extraction/separation of chromium species on solid sorbents and liquid-liquid extraction of chromium species. The most popular strategy is that based on solid-phase extraction. Therefore, this review shows the potential of novel materials designed and used for selective binding of chromium species. The progress in miniaturization of measurement systems is also presented.

Soybean plant growth study conducted using purified protein hydrolysate-based fertilizer made from chrome-tanned leather waste.

PubMed

Pati, Anupama; Chaudhary, Rubina

2015-12-01

Leather processing discharges enormous amount of chrome containing leather solid waste which creates a major disposal problem. Chrome-tanned leather solid waste is a complex of collagen and chromium. The presence of chromium limits protein application in fertilizer industry. The purified protein hydrolysate with zero chromium could be used as a nitrogen source for fertilizer formulation. In this study, an attempt has been made to employ purified protein hydrolysate derived from chrome-tanned leather shavings (CTLS) in formulation of fertilizer. The formulated fertilizer (1–3 t ha(-1)) is employed as nitrogen source in production of soybean. Plant growth study demonstrates that formulated fertilizer dosage 3 t ha(-1) produced similar effects of commercial fertilizer-treated plants. Application of formulated fertilizer yielded higher seed in plant than commercial fertilizer.

A Case of Chromium Contact Dermatitis due to Exposure from a Golf Glove.

PubMed

Lim, Jong Ho; Kim, Hei Sung; Park, Young Min; Lee, Jun Young; Kim, Hyung Ok

2010-02-01

Chromium is a transition metal and has been shown to elicit contact dermatitis. Although leather products have been known to be the most significant source of chromium exposure these days, the majority of reports have been related to exposure from shoe products. We herein report a professional golfer who became allergic to golf gloves made of chromium-tanned leather. A 27-year-old woman golfer presented with recurrent, pruritic, erythematous plaques that had been occurring on both hands for several years. The lesions developed whenever she had worn golf gloves for an extended period of time, especially during tournament season. To identify the causative agent, patch tests were performed and the results demonstrated a strong positive reaction to potassium dichromate 0.5% and to her own glove. The amount of chromium in her golf glove was analyzed to be 308.91 ppm and based on this, a diagnosis of allergic contact dermatitis due to a chromium-tanned leather glove was made. She was treated with oral antihistamines combined with topical steroids and advised to wear chromium-free leather gloves. There has been no evidence of recurrence during a six month follow-up period.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Gilbert, H.K.

Research objectives were to study the effect of food source, preparation method and chemical form on bioavailability of chromium. Chromium concentration in potatoes was determined and tubers labeled either intrinsically or extrinsically with radioactive chromate. A labeled chromium complexes was isolated from preparations of raw, baked or fried potatoes and chromatographed on gel permeation media. Availability of the potato chromium complex to the rat was examined in three feeding studies. Animals were dosed with radioactive extrinsically or intrinsically labeled potato extract or with chromate. A labeled chromium complex was isolated from gastrointestinal contents of rats and chromatographed. Potato pulp andmore » peel contained 1.63 and 2.70 ..mu..g Cr/g tissue respectively. True and apparent absorption from extrinsically labeled feedings were 33.4 +/- 4.7 and 29.8 +/- 11.2% respectively, and no differences existed between absorption from raw and cooked potatoes. Absorption from the extrinsic labeled potatoes differed significantly from absorption of inorganic chromatium. Apparent absorption of raw (11.1 +/- 7.9%) and cooked (-0.7 +/- 2.8%) intrinsically labeled feedings differed significantly. Absorption of inorganic chromium was 17.8% (true) and 11.5% (apparent). Examination of the chromium complex isolated from gastrointestinal tract contents showed enlargement of the complex in the stomach after consumption.« less

40 CFR 421.226 - Pretreatment standards for new sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

... molybdenum produced Arsenic 27.120 12.097 Chromium 7.219 2.927 Lead 5.463 2.536 Nickel 10.731 7.219 Iron 23... technical grade molybdenum plus vanadium plus pure grade molybdenum produced Arsenic 80.952 36.108 Chromium...] [Reserved] Ammonia (as N) 24114.000 10600.000 (c) Vanadium decomposition wet air pollution control. PSNS for...

40 CFR 421.226 - Pretreatment standards for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... molybdenum produced Arsenic 27.120 12.097 Chromium 7.219 2.927 Lead 5.463 2.536 Nickel 10.731 7.219 Iron 23... technical grade molybdenum plus vanadium plus pure grade molybdenum produced Arsenic 80.952 36.108 Chromium...] [Reserved] Ammonia (as N) 24114.000 10600.000 (c) Vanadium decomposition wet air pollution control. PSNS for...

78 FR 20642 - Notice of Proposed CERCLA Agreement and Order on Consent for Removal Action by Bona Fide...

Federal Register 2010, 2011, 2012, 2013, 2014

2013-04-05

... Fernando Valley Area 2 Superfund Site, Glendale Chromium Operable Unit, 264 W. Spazier Ave., Burbank... Site, Glendale Chromium Operable Unit, located at 264 W. Spazier Ave., Burbank, California. Under the...

Process for the Production of Star Tracklng [Tracking] Reticles

NASA Technical Reports Server (NTRS)

Smith, Wade O. (Inventor); Toft, Albert R. (Inventor)

1972-01-01

A method for the production of reticles, particularly those for use in outer space, wherein the product is a quartz base coated with highly adherent layers of chromium, chromium-silver, and silver vacuum deposited through a mask, and then coated with an electrodeposit of copper from a copper sulfate solution followed by an electrodeposit of black chromium. The masks are produced by coating a beryllium-copper alloy substrate with a positive working photoresist, developing the photoresist according to a pattern to leave a positive mask, plating uncoated areas with gold, removing the photoresist, coating the substrate with a negative working photoresist, developing the negative working photoresist to expose the base metal of the pattern, and chemically etching the unplated side of the pattern to produce the mask. The mask produced is then used in the vacuum deposition of: (1) chromium metal on the surface of a quartz base to obtain a highly adherent quartz-chromium interface; (2) silver on the chromium deposit, during the final stage of chromium deposit, to produce a silver chromium alloy layer; and (3) silver onto the surface of the alloy layer. The coated quartz base is then coated by electroplating utilizing an acid copper deposit followed by a black chromium electrodeposit to produce the product of the present invention.

Surface decoration through electrostatic interaction leading to enhanced reactivity: Low temperature synthesis of nanostructured chromium borides (CrB and CrB{sub 2})

DOE Office of Scientific and Technical Information (OSTI.GOV)

Menaka,; Kumar, Bharat; Kumar, Sandeep

The present study describes a novel low temperature route at ambient pressure for the synthesis of nanocrystalline chromium borides (CrB and CrB{sub 2}) without using any flux or additives. The favorable and intimate mixing of nanoparticles of chromium acetate (Cr source) and boron forms an active chromium–boron precursor which decomposes at much lower temperature (400 °C) to form CrB (which is ∼1000 °C less than the known ambient pressure synthesis). The chromium acetate nanoparticles (∼5 nm) decorate the larger boron particles (150–200 nm) due to electrostatic interactions resulting from opposing surface charges of boron (zeta potential:+48.101 mV) and chromium acetatemore » (zeta potential:−4.021 mV) in ethanolic medium and is evident in the TEM micrographs. The above method leads to the formation of pure CrB film like structure at 400 °C and nanospheres (40–60 nm) at 600 °C. Also, chromium diboride (CrB{sub 2}) nanoparticles (25 nm) could be obtained at 1000 °C. - Graphical abstract: Variation of surface charge of reactants, precursor and the products, chromium borides (CrB and CrB{sub 2}). Highlights: ► Novel borothermal reduction process for synthesis of chromium boride. ► Significant lowering of reaction temperature to obtain nanocrystalline chromium boride. ► Enhanced reactivity due to appropriate surface interactions.« less

Water Consumption as Source of Arsenic, Chromium, and Mercury in Children Living in Rural Yucatan, Mexico: Blood and Urine Levels.

PubMed

Arcega-Cabrera, F; Fargher, L F; Oceguera-Vargas, I; Noreña-Barroso, E; Yánez-Estrada, L; Alvarado, J; González, L; Moo-Puc, R; Pérez-Herrera, N; Quesadas-Rojas, M; Pérez-Medina, S

2017-10-01

Studies investigating the correlation between metal content in water and metal levels in children are scarce worldwide, but especially in developing nations. Therefore, this study investigates the correlation between arsenic, chromium, and mercury concentrations in drinking and cooking water and in blood and urine samples collected from healthy and supposedly non-exposed children from a rural area in Yucatan, Mexico. Mercury in water shows concentrations above the recommended World Health Organization (WHO) value for drinking and cooking water. Also, 25% of the children show mercury in urine above the WHO recommended value. Multivariate analyses show a significant role for drinking and cooking water as a vector of exposure in children. Also, the factor analysis shows chronic exposure in the case of arsenic, as well as an ongoing detoxification process through urine in the case of mercury. Further studies should be done in order to determine other potential metal exposure pathways among children.

Occurrence and risk assessment of potentially toxic elements and typical organic pollutants in contaminated rural soils.

PubMed

Xu, Yongfeng; Dai, Shixiang; Meng, Ke; Wang, Yuting; Ren, Wenjie; Zhao, Ling; Christie, Peter; Teng, Ying

2018-07-15

The residual levels and risk assessment of several potentially toxic elements (PTEs), phthalate esters (PAEs) and polycyclic aromatic hydrocarbons (PAHs) in rural soils near different types of pollution sources in Tianjin, China, were studied. The soils were found to be polluted to different extents with PTEs, PAEs and PAHs from different pollution sources. The soil concentrations of chromium (Cr), nickel (Ni), di-n-butyl phthalate (DnBP), acenaphthylene (Any) and acenaphthene (Ane) were higher than their corresponding regulatory reference limits. The health risk assessment model used to calculate human exposure indicates that both non-carcinogenic and carcinogenic risks from selected pollutants were generally acceptable or close to acceptable. Different types of pollution sources and soil physicochemical properties substantially affected the soil residual concentrations of and risks from these pollutants. PTEs in soils collected from agricultural lands around industrial and residential areas and organic pollutants (PAEs and PAHs) in soils collected from agricultural areas around livestock breeding were higher than those from other types of pollution sources and merit long-term monitoring. Copyright © 2018 Elsevier B.V. All rights reserved.

Microstructure and corrosion resistance of sputter-deposited titanium-chromium alloy coatings

DOE Office of Scientific and Technical Information (OSTI.GOV)

Landolt, D.; Robyr, C.; Mettraux, P.

1998-10-01

Titanium, chromium, and titanium-chromium alloy coatings were sputter-deposited to study their corrosion behaviors in relation to microstructure and composition. Silicon substrates were used to study the effect of alloying on intrinsic corrosion resistance of the coating materials, and brass substrates were used to study the effect of alloying on the penetrating porosity of the coatings. Corrosion behavior was characterized using linear sweep voltammetry. The crystal structure of the coatings was examined by x-ray diffraction (XRD) and the microstructure by scanning electron microscopy (SEM). Electrochemical impedance spectroscopy (EIS) was used to estimate the real surface area of the coatings. Results showedmore » alloying of titanium with chromium greatly influenced microstructure of the coatings. Alloying led to deposits of higher apparent density and, in some cases, to an x-ray amorphous structure. Alloy coatings showed significantly lower corrosion currents than the constituting metals. The effect was attributed to a smoother surface topography. When corrected of differences in real surface area, the intrinsic corrosion rate of the alloy coatings did not differ significantly from that of the constituting metals. Alloy coatings deposited on brass exhibited a lower porosity than titanium or chromium metal coatings produced under identical conditions.« less

Chromium Toxicity Test for Fall Chinook Salmon (Oncorhynchus tshawytscha) Using Hanford Site Groundwater: Onsite Early Life-Stage Toxicity Evaluation

DOE Office of Scientific and Technical Information (OSTI.GOV)

Patton, Gregory W; Dauble, Dennis D; Chamness, Mickie A

The objective of this study was to evaluate site-specific effects for early life-stage (eyed eggs to free swimming juveniles) fall chinook salmon that might be exposed to hexavalent chromium from Hanford groundwater sources. Our exposure conditions included hexavalent chromium obtained from Hanford groundwater wells near the Columbia River, Columbia River water as the diluent, and locally adapted populations of fall chinook salmon. This report describes both a 96-hr pretest using rainbow trout eggs and an early life-stage test beginning with chinook salmon eggs.

Biological groundwater treatment for chromium removal at low hexavalent chromium concentrations.

PubMed

Mamais, Daniel; Noutsopoulos, Constantinos; Kavallari, Ioanna; Nyktari, Eleni; Kaldis, Apostolos; Panousi, Eleni; Nikitopoulos, George; Antoniou, Kornilia; Nasioka, Maria

2016-06-01

The objective of this work is to develop and evaluate biological groundwater treatment systems that will achieve hexavalent chromium reduction and total chromium removal from groundwater at hexavalent chromium (Cr(VI)) groundwater concentrations in the 0-200 μg/L range. Three lab-scale units operated, as sequencing batch reactors (SBR) under aerobic, anaerobic and anaerobic-aerobic conditions. All systems received groundwater with a Cr(VI) content of 200 μg/L. In order to support biological growth, groundwater was supplemented with milk, liquid cheese whey or a mixture of sugar and milk to achieve a COD concentration of 200 mg/L. The results demonstrate that a fully anaerobic system or an anaerobic-aerobic system dosed with simple or complex external organic carbon sources can lead to practically complete Cr(VI) reduction to Cr(III). The temperature dependency of maximum Cr(VI) removal rates can be described by the Arrhenius relationship. Total chromium removal in the biological treatment systems was not complete because a significant portion of Cr(III) remained in solution. An integrated system comprising of an anaerobic SBR followed by a sand filter achieved more than 95% total chromium removal thus resulting in average effluent total and dissolved chromium concentrations of 7 μg/L and 3 μg/L, respectively. Copyright © 2016 Elsevier Ltd. All rights reserved.

CHROMIUM PLATING FOR PROTECTION AGAINST STRESS CORROSION CRACKING OF HARDENED AISI 410 STEEL

DOE Office of Scientific and Technical Information (OSTI.GOV)

Suss, H.

1958-04-22

Because of its high corrosion resistance properties, chromium electroplate should offer protection to AISI 419 steel against stress corrosion cracking. Tests have been made (KAPL and Bettis) on chromium plates on test specimens as deposited by two different sources in conformance with Bettis and USMC specifications. These deposits either offered protection to hardened (RC36- 42) AISI 410 against stress corrosion cracking, or caused accelerated stress corrosion cracking under conditions which did not crack unplated material. At present there is no significant data which could give definite clues for these extreme differences in the corrosive protective values. The results of testsmore » so far strongly question tbe value of chromium plate as a means to protect AISI 410 against stress corrosion cracking. (A.C.)« less

40 CFR 437.16 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2010 CFR

2010-07-01

...) EFFLUENT GUIDELINES AND STANDARDS THE CENTRALIZED WASTE TREATMENT POINT SOURCE CATEGORY Metals Treatment... standards: Standards for antimony, arsenic, cadmium, chromium, cobalt, copper, lead, mercury, nickel, silver...

40 CFR 421.224 - Standards of performance for new sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

... plus vanadium plus pure grade molybdenum produced Arsenic 27.120 12.097 Chromium 7.219 2.927 Lead 5.463... produced Arsenic 80.952 36.108 Chromium 21.548 8.736 Lead 16.306 7.571 Nickel 32.031 21.548 Iron 69.887 35... pollution control. NSPS for the Secondary Molybdenum and Vanadium Subcategory Pollutant or pollutant...

40 CFR 421.224 - Standards of performance for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... plus vanadium plus pure grade molybdenum produced Arsenic 27.120 12.097 Chromium 7.219 2.927 Lead 5.463... produced Arsenic 80.952 36.108 Chromium 21.548 8.736 Lead 16.306 7.571 Nickel 32.031 21.548 Iron 69.887 35... pollution control. NSPS for the Secondary Molybdenum and Vanadium Subcategory Pollutant or pollutant...

40 CFR 468.15 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... average Metric units—mg/off-kg of copper or copper alloy hot rolled English units—pounds per 1,000,000 off... English units—pounds per 1,000,000 off-pounds of copper or copper alloy cold rolled Chromium 0.140 0.056... copper alloy drawn English units—pounds per 1,000,000 off-pounds of copper or copper alloy drawn Chromium...

Automatic flow system for simultaneous determination of iron and chromium in steel alloys employing photometers based on LEDs as radiation source

PubMed Central

Fernandes, Ridvan N.; Campos, Luís Fernando P.

2003-01-01

A multicommutated flow system for simultaneous determination of iron and chromium in steel alloys by photometry is described. The flow network consisted of an automatic injector and four solenoid valves assembled to form two independent analytical pathways, each one comprising reaction coils and a flow cell. The light source (LED) and detector (photodiode) were attached to the flow cells to form a compact unit. The flow system was microcomputer controlled by Quick BASIC 4.5 software, which carried out all steps of the analytical procedure. The feasibility of the system was proved by the determination of iron and chromium in steel alloys and its accuracy was accessed by comparing results with those obtained by plasma atomic emission spectrometry (ICP-AES). No significant difference at the 95% confidence level was observed. Other profitable features such as low reagent consumption (0.33 mg 1,10-phenantroline and 0.03 mg 1,5-diphenylcarbazide per determination); relative standard deviations (n = 5) of 0.4% for iron and 1.2% for chromium; and an analytical throughput of 160 determinations per h were also achieved. PMID:18924884

Dynamics of Hexavalent Chromium in Four Types of Aquaculture Ponds and Its Effects on the Morphology and Behavior of Cultured Clarias gariepinus (Burchell 1822).

PubMed

Mustapha, Moshood Keke

2017-04-01

Hexavalent chromium is a bio accumulative toxic metal in water and fish. It enters aquaculture ponds mainly through anthropogenic sources. Hexavalent chromium concentrations and its effects on the morphology and behavior of Clarias gariepinus were investigated from four aquaculture ponds for 12 weeks. Chromium was measured using diphenyl carbohdrazide method; alkalinity and hardness were measured using colometric method and analyzed with Bench Photometer. Temperature and pH were measured using pH/EC/TDS/Temp combined tester. Temporal and spatial replications of samples were done with triplicates morphological and behavioural effects of the metal on fish were observed visually. Chromium ranged from no detection to 0.05 mg/L, alkalinity 105 to 245 mg/L, hardness 80 to 165 mg/L, pH 6.35 to 8.03 and temperature 29.1 to 35.9°C. Trend in the chromium concentrations in the ponds is natural > earthen > concrete > collapsible. There was a significant difference ( P < 0.05) in chromium, alkalinity, water hardness, pH and temperature among the four ponds. Significant positive correlation also existed between alkalinity, water hardness, pH, with chromium. Morphological and behavioural changes observed in the fish include irregular swimming, frequent coming to the surface, dark body colouration, mucous secretion on the body, erosion of gill epithelium, fin disintegration, abdominal distension and lethargy. High chromium concentration in natural pond was due to anthropogenic run-off of materials in to the pond. Acidic pH, low alkalinity, low water hardness also contributed to the high chromium concentration. Morphological and behavioural changes observed were attributed to the high concentrations, toxicity and bio accumulative effect of the metal. Toxicity of chromium to fish in aquaculture could threaten food security. Watershed best management practices and remediation could be adopted to reduce the effects of toxicity of chromium on pond water quality, fish flesh quality and fish welfare.

In which regions is breast-feeding safer from the impact of toxic elements from the environment?

PubMed

Cinar, Nursan; Ozdemir, Sami; Yucel, Oya; Ucar, Fatma

2011-11-01

Owing to its unique nutritional and immunological characteristics, breast milk is the most important food source for infants. But, children are at greater risk for exposure to environmental toxicants from breast milk. The aim of this study was to evaluate the influence of environmental pollution on essential and toxic element contents of breast milk and determine the risky locations in our population. This study was conducted on women who were breastfeeding (n=90). Milk samples were collected at three locations in Marmara region, Turkey: highly industrialized region highly affected by pollution, urbanized region moderately and rural area that is affected little. Breast milk samples (5 mL) were collected at approximately one month postpartum (mature milk). The concentrations of cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), iron (Fe), manganese (Mn), nickel (Ni), lead (Pb) and zinc (Zn) in milk samples were compared to the milk samples coming from different locations.Lead, cadmium, nickel, chromium, iron and manganese levels in the breast milk are highest and engrossing especially in rural areas compared to the other regions but cobalt, copper, zinc levels are highest in highly industrial areas. The levels of essential and toxic elements in breast milk can vary in different regions. The levels presented in our study are above some countries' data albeit not at toxic levels. Because of global effects, environmental pollution is not the problem for industrializing regions only. Rural area also may not be safe for breastfeed babies.

Phytochemical and Biological Activities of Four Wild Medicinal Plants

PubMed Central

Ahmad, Shabir; AbdEl-Salam, Naser M.; Fouad, H.; Rehman, Najeeb Ur; Hussain, Hidayat; Saeed, Wajid

2014-01-01

The fruits of four wild plants, namely, Capparis decidua, Ficus carica, Syzygium cumini, and Ziziphus jujuba, are separately used as traditional dietary and remedial agents in remote areas of Khyber Pakhtunkhwa, Pakistan. The results of our study on these four plants revealed that the examined fruits were a valuable source of nutraceuticals and exhibited good level of antimicrobial activity. The fruits of these four investigated plants are promising source of polyphenols, flavonoids, alkaloids, terpenoids, and saponins. These four plants' fruits are good sources of iron, zinc, copper, manganese, selenium, and chromium. It was also observed that these fruits are potential source of antioxidant agent and the possible reason could be that these samples had good amount of phytochemicals. Hence, the proper propagation, conservation, and chemical investigation are recommended so that these fruits should be incorporated for the eradication of food and health related problems. PMID:25374941

40 CFR 437.15 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2010 CFR

2010-07-01

...) EFFLUENT GUIDELINES AND STANDARDS THE CENTRALIZED WASTE TREATMENT POINT SOURCE CATEGORY Metals Treatment..., cadmium, chromium, cobalt, copper, lead, mercury, nickel, silver, tin, titanium, vanadium, and zinc are...

Spectroscopic and biological activity studies of the chromium-binding peptide EEEEGDD.

PubMed

Arakawa, Hirohumi; Kandadi, Machender R; Panzhinskiy, Evgeniy; Belmore, Kenneth; Deng, Ge; Love, Ebony; Robertson, Preshus M; Commodore, Juliette J; Cassady, Carolyn J; Nair, Sreejayan; Vincent, John B

2016-06-01

While trivalent chromium has been shown at high doses to have pharmacological effects improving insulin resistance in rodent models of insulin resistance, the mechanism of action of chromium at a molecular level is not known. The chromium-binding and transport agent low-molecular-weight chromium-binding substance (LMWCr) has been proposed to be the biologically active form of chromium. LMWCr has recently been shown to be comprised of a heptapeptide of the sequence EEEEDGG. The binding of Cr(3+) to this heptapeptide has been examined. Mass spectrometric and a variety of spectroscopic studies have shown that multiple chromic ions bind to the peptide in an octahedral fashion through carboxylate groups and potentially small anionic ligands such as oxide and hydroxide. A complex of Cr and the peptide when administered intravenously to mice is able to decrease area under the curve in intravenous glucose tolerance tests. It can also restore insulin-stimulated glucose uptake in myotubes rendered insulin resistant by treating them with a high-glucose media.

Comparison of Ultrasound-Assisted and Regular Leaching of Vanadium and Chromium from Roasted High Chromium Vanadium Slag

NASA Astrophysics Data System (ADS)

Wen, Jing; Jiang, Tao; Gao, Huiyang; Liu, Yajing; Zheng, Xiaole; Xue, Xiangxin

2018-02-01

Ultrasound-assisted leaching (UAL) was used for vanadium and chromium leaching from roasted material obtained by the calcification roasting of high-chromium-vanadium slag. UAL was compared with regular leaching. The effect of the leaching time and temperature, acid concentration, and liquid-solid ratio on the vanadium and chromium leaching behaviors was investigated. The UAL mechanism was determined from particle-size-distribution and microstructure analyses. UAL decreased the reaction time and leaching temperature significantly. Furthermore, 96.67% vanadium and less than 1% chromium were leached at 60°C for 60 min with 20% H2SO4 at a liquid-solid ratio of 8, which was higher than the maximum vanadium leaching rate of 90.89% obtained using regular leaching at 80°C for 120 min. Ultrasonic waves broke and dispersed the solid sample because of ultrasonic cavitation, which increased the contact area of the roasted sample and the leaching medium, the solid-liquid mass transfer, and the vanadium leaching rate.

Characterization and Performance of a High-Current-Density Ion Implanter with Magnetized Hollow-Cathode Plasma Source

NASA Astrophysics Data System (ADS)

Falkenstein, Zoran; Rej, Donald; Gavrilov, Nikolai

1998-10-01

In a collaboration between the Institute of Electrophysics (IEP) and the Los Alamos National Laboratory (LANL), the IEP has developed an industrial scalable, high-power, large-area ion source for the surface modification of materials. The plasma source of the ion beam source can be described as a pulsed glow discharge with a cold, hollow-cathode in a weak magnetic field. Extraction and focusing of positive ions by an acceleration and ion-optical plate system renders the generation of a homogeneous, large-area ion beam with an averaged total ion current of up to 50 mA at acceleration voltages of up to 50 kV. The principle set-up of the ion beam source as well as some electrical characteristics (gas discharge current and the extracted ion beam current) are presented for a lab-scale prototype. Measurements of the radial ion current density profiles within the ion beam for various discharge parameters, as well as results on surface modification by ion implantation of nitrogen into aluminum and chromium are presented. Finally, a comparison of the applied ion dose with the retained ion doses is given.

40 CFR 467.46 - Pretreatment standards for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... off-lbs) of aluminum forged Chromium 0.019 0.008 Cyanide 0.010 0.004 Zinc 0.051 0.021 TTO 0.035 Oil and grease (alternate monitoring parameter) 0.50 0.50 Subpart D Forging Scrubber Liquor Pollutant or... aluminum forged Chromium 0.035 0.014 Cyanide 0.019 0.008 Zinc 0.096 0.040 TTO 0.065 Oil and grease...

40 CFR 471.85 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... Chromium 0.133 0.054 Copper 0.459 0.219 Cyanide 0.072 0.029 Zinc 0.365 0.151 (j) Alkaline cleaning spent... mg/off-kg (pounds per million off-pounds) of zinc alkaline cleaned Chromium 0.002 0.0006 Copper 0.005 0.002 Cyanide 0.0007 0.0003 Zinc 0.004 0.002 (k) Alkaline cleaning rinse. Subpart H—PSNS Pollutant...

40 CFR 471.85 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... Chromium 0.133 0.054 Copper 0.459 0.219 Cyanide 0.072 0.029 Zinc 0.365 0.151 (j) Alkaline cleaning spent... mg/off-kg (pounds per million off-pounds) of zinc alkaline cleaned Chromium 0.002 0.0006 Copper 0.005 0.002 Cyanide 0.0007 0.0003 Zinc 0.004 0.002 (k) Alkaline cleaning rinse. Subpart H—PSNS Pollutant...

40 CFR 471.85 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... Chromium 0.133 0.054 Copper 0.459 0.219 Cyanide 0.072 0.029 Zinc 0.365 0.151 (j) Alkaline cleaning spent... mg/off-kg (pounds per million off-pounds) of zinc alkaline cleaned Chromium 0.002 0.0006 Copper 0.005 0.002 Cyanide 0.0007 0.0003 Zinc 0.004 0.002 (k) Alkaline cleaning rinse. Subpart H—PSNS Pollutant...

Determination of total Cr in wastewaters of Cr electroplating factories in the I.organize industry region (Kayseri, Turkey) by ICP-AES.

PubMed

Yilmaz, Selehattin; Türe, Melike; Sadikoglu, Murat; Duran, Ali

2010-08-01

The wastewater pollution in industrial areas is one of the most important environmental problems. Heavy metal pollution, especially chromium pollution in the wastewater sources from electroplating, dyeing, and tannery, has affected the life on earth. This pollution can affect on all ecosystems and human health directly or by food chain. Therefore, the determination of total chromium in this study is of great importance. In this study, accurate, rapid, sensitive, selective, simple, and low-cost technique for the direct determination of total Cr in wastewater samples collected from the some Cr electroplating factories in March 2008 by inductively coupled plasma-atomic emission spectrometry has been developed. The analysis of a given sample is completed in about 15 min by this technique applied. As the result of the chromium analysis, the limit of quantification for the total Cr were founded to be over the limit value (0.05 mg L(-1); WHO, EPA, TSE 266, and inland water quality classification) as 1,898.78+/-0.34 mg/L at station 1 and 3,189.02+/-0.56 mg/L at station 2. The found concentration of total Cr has been determined to be IV class quality water according to the inland water classification. In order to validate the applied method, recovery studies were performed.

Method for welding chromium molybdenum steels

DOEpatents

Sikka, Vinod K.

1986-01-01

Chromium-molybdenum steels exhibit a weakening after welding in an area adjacent to the weld. This invention is an improved method for welding to eliminate the weakness by subjecting normalized steel to a partial temper prior to welding and subsequently fully tempering the welded article for optimum strength and ductility.

Toxic and genotoxic effects of hexavalent chromium in environment and its bioremediation strategies.

PubMed

Mishra, Sandhya; Bharagava, Ram Naresh

2016-01-01

Chromium is one of the major inorganic environmental pollutants, which is added in the environment through various natural and anthropogenic activities and exists mainly in two forms: Cr(III) and Cr(VI). Cr(VI) is considered to be more toxic than Cr(III) due to its high solubility and mobility. It is a well-reported occupational carcinogen associated with lung, nasal, and sinus cancers. Thus, this review article provides the detailed information on the occurrence, sources of chromium contamination in the environment and their toxicological effects in human, animal, plants as well as in microorganisms, and bioremediation strategies to minimize the toxic effects.

40 CFR 467.26 - Pretreatment standards for new sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

... GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions... for monthly average mg/off-kg (lb/million off-lbs) of aluminum rolled with emulsions Chromium 0.048 0...

40 CFR 467.64 - New source performance standards.

Code of Federal Regulations, 2014 CFR

2014-07-01

... GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions or Soaps... for monthly average mg/off-kg (lb/million off-lbs) of aluminum drawn with emulsions or soaps Chromium...

40 CFR 467.64 - New source performance standards.

Code of Federal Regulations, 2011 CFR

2011-07-01

... GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions or Soaps Subcategory... for monthly average mg/off-kg (lb/million off-lbs) of aluminum drawn with emulsions or soaps Chromium...

40 CFR 467.66 - Pretreatment standards for new sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

... GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions or Soaps... for monthly average mg/off-kg (lb/million off-lbs) of aluminum drawn with emulsions or soaps Chromium...

40 CFR 467.26 - Pretreatment standards for new sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

... GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions... for monthly average mg/off-kg (lb/million off-lbs) of aluminum rolled with emulsions Chromium 0.048 0...

40 CFR 467.66 - Pretreatment standards for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions or Soaps Subcategory... for monthly average mg/off-kg (lb/million off-lbs) of aluminum drawn with emulsions or soaps Chromium...

40 CFR 467.26 - Pretreatment standards for new sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

... GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions... for monthly average mg/off-kg (lb/million off-lbs) of aluminum rolled with emulsions Chromium 0.048 0...

40 CFR 467.66 - Pretreatment standards for new sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

... GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions or Soaps... for monthly average mg/off-kg (lb/million off-lbs) of aluminum drawn with emulsions or soaps Chromium...

40 CFR 467.64 - New source performance standards.

Code of Federal Regulations, 2012 CFR

2012-07-01

... GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions or Soaps... for monthly average mg/off-kg (lb/million off-lbs) of aluminum drawn with emulsions or soaps Chromium...

40 CFR 467.66 - Pretreatment standards for new sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

... GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions or Soaps... for monthly average mg/off-kg (lb/million off-lbs) of aluminum drawn with emulsions or soaps Chromium...

40 CFR 467.64 - New source performance standards.

Code of Federal Regulations, 2013 CFR

2013-07-01

... GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions or Soaps... for monthly average mg/off-kg (lb/million off-lbs) of aluminum drawn with emulsions or soaps Chromium...

Environmental exposure to chromium compounds in the valley of León, México.

PubMed Central

Armienta-Hernández, M A; Rodríguez-Castillo, R

1995-01-01

The effects on the environment and health of the operation of a chromate compounds factory and tanneries in the León valley in central México are discussed. Sampling and analysis of chromium were performed in water, soil, and human urine. Groundwater has been polluted in an area of about 5 km2 by the leaching of a solid factory waste, which results in concentrations up to 50 mg/l of hexavalent chromium. The plume shape and extension appear to be controlled by the prevailing well extraction regime. Total chromium was detected in the soil around the factory as a result of both aerial transport and deposition of dust produced in the chromate process and irrigation with tannery-contaminated water. Analysis of the impact of chromium in air and water on populations with various degrees of exposure revealed that highly harmful health effects were not observed. PMID:7621799

Study of the formation of thermochemical laser-induced periodic surface structures on Cr, Ti, Ni and NiCr films under femtosecond irradiation

NASA Astrophysics Data System (ADS)

Dostovalov, A. V.; Korolkov, V. P.; Terentyev, V. S.; Okotrub, K. A.; Dultsev, F. N.; Babin, S. A.

2017-07-01

The formation of femtosecond laser-induced periodic surface structures (LIPSS's) on Cr, Ti, Ni and NiCr films (with different Cr contents) is investigated. It is established that thermochemical LIPSS's with periods of 950, 930 and 980 nm are formed, respectively, on the surfaces of titanium, chromium, and nichrome (with a chromium content of 20%); however, thermochemical LIPSS's are not formed on the surfaces of nickel and nichrome with a low chromium content, although Raman data indicate that oxidation occurs in all cases. A weakly ordered ablated structure with a period of 250-300 nm is found to be formed on oxidised areas of thermochemical LIPSS's in the case of chromium and nichrome (80/20). Experimental data on selective etching of thermochemical LIPSS's on titanium and chromium films are presented.

Effects of land use on ground-water quality in central Florida; preliminary results, US Geological Survey Toxic Waste-Ground Water Contamination Program

USGS Publications Warehouse

Rutledge, A.T.

1987-01-01

Groundwater is the principal source of drinking water in central Florida. The most important hydrogeologic unit is the Floridan aquifer system, consisting of fractured limestone and dolomite limestone. Activities of man in areas of recharge to the Floridian aquifer system that may be affecting groundwater quality include: (1) the use of drainage wells for stormwater disposal in urban areas, (2) the use of pesticides and fertilizers in citrus groves, and (3) the mining and processing of phosphate ore in mining areas. Preliminary findings about the impacts of these land uses on ground-water quality by comparison with a fourth land use representing the absence of human activity in another area of recharge are presented. Drainage wells convey excess urban stormwater directly to the Upper Floridian aquifer. The volatile organic compounds are the most common contaminants in ground water. Trace elements such as chromium and lead are entering the aquifer but their movement is apparently attenuated by precipitation reactions associated with high pH or by cation-exchange reactions. Among the trace elements and organic chemicals, most ground-water contamination in citrus production areas is caused by pesticides, which include the organic compounds simazine, ametryne, chlordane, DDE , bromacil, aldicarb, EDB, trifluralin, and diazinon, and the trace elements zinc and copper; other contaminants include benzene, toluene, napthalene, and indene compounds. In the phosphate mining area, constituents of concern are arsenic, selenium, and mercury, and secondarily lead, chromium, cadmium, and others. Organic compounds such as fluorene, naphthalene, di-n-butyl phthalate, alkylated benzenes and naphthalenes, and indene compounds also are entering groundwater. (Author 's abstract)

40 CFR 467.24 - New source performance standards.

Code of Federal Regulations, 2011 CFR

2011-07-01

... GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions Subcategory § 467.24... for monthly average mg/off-kg (lb/million off-lbs) of aluminum rolled with emulsions Chromium 0.048 0...

40 CFR 471.24 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2013 CFR

2013-07-01

... Chromium 0.033 0.014 Zinc 0.109 0.046 Ammonia 9.95 4.37 Fluoride 4.44 1.97 (b) Forging spent lubricants....422 0.177 Ammonia 38.5 17.0 Fluoride 17.2 7.63 (d) Forging equipment cleaning wastewater. Subpart B... (pounds per million off-pounds) of magnesium forged Chromium 0.002 0.0007 Zinc 0.006 0.003 Ammonia 0.532 0...

40 CFR 471.24 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2012 CFR

2012-07-01

... Chromium 0.033 0.014 Zinc 0.109 0.046 Ammonia 9.95 4.37 Fluoride 4.44 1.97 (b) Forging spent lubricants....422 0.177 Ammonia 38.5 17.0 Fluoride 17.2 7.63 (d) Forging equipment cleaning wastewater. Subpart B... (pounds per million off-pounds) of magnesium forged Chromium 0.002 0.0007 Zinc 0.006 0.003 Ammonia 0.532 0...

40 CFR 471.24 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2011 CFR

2011-07-01

... Chromium 0.033 0.014 Zinc 0.109 0.046 Ammonia 9.95 4.37 Fluoride 4.44 1.97 (b) Forging spent lubricants....422 0.177 Ammonia 38.5 17.0 Fluoride 17.2 7.63 (d) Forging equipment cleaning wastewater. Subpart B... (pounds per million off-pounds) of magnesium forged Chromium 0.002 0.0007 Zinc 0.006 0.003 Ammonia 0.532 0...

40 CFR 471.24 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2010 CFR

2010-07-01

... Chromium 0.033 0.014 Zinc 0.109 0.046 Ammonia 9.95 4.37 Fluoride 4.44 1.97 (b) Forging spent lubricants....422 0.177 Ammonia 38.5 17.0 Fluoride 17.2 7.63 (d) Forging equipment cleaning wastewater. Subpart B... (pounds per million off-pounds) of magnesium forged Chromium 0.002 0.0007 Zinc 0.006 0.003 Ammonia 0.532 0...

40 CFR 471.24 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2014 CFR

2014-07-01

... Chromium 0.033 0.014 Zinc 0.109 0.046 Ammonia 9.95 4.37 Fluoride 4.44 1.97 (b) Forging spent lubricants....422 0.177 Ammonia 38.5 17.0 Fluoride 17.2 7.63 (d) Forging equipment cleaning wastewater. Subpart B... (pounds per million off-pounds) of magnesium forged Chromium 0.002 0.0007 Zinc 0.006 0.003 Ammonia 0.532 0...

Source Identification and Apportionment of Trace Elements in Soils in the Yangtze River Delta, China.

PubMed

Shao, Shuai; Hu, Bifeng; Fu, Zhiyi; Wang, Jiayu; Lou, Ge; Zhou, Yue; Jin, Bin; Li, Yan; Shi, Zhou

2018-06-12

Trace elements pollution has attracted a lot of attention worldwide. However, it is difficult to identify and apportion the sources of multiple element pollutants over large areas because of the considerable spatial complexity and variability in the distribution of trace elements in soil. In this study, we collected total of 2051 topsoil (0⁻20 cm) samples, and analyzed the general pollution status of soils from the Yangtze River Delta, Southeast China. We applied principal component analysis (PCA), a finite mixture distribution model (FMDM), and geostatistical tools to identify and quantitatively apportion the sources of seven kinds of trace elements (chromium (Cr), cadmium (Cd), mercury (Hg), copper (Cu), zinc (Zn), nickel (Ni), and arsenic (As)) in soil. The PCA results indicated that the trace elements in soil in the study area were mainly from natural, multi-pollutant and industrial sources. The FMDM also fitted three sub log-normal distributions. The results from the two models were quite similar: Cr, As, and Ni were mainly from natural sources caused by parent material weathering; Cd, Cu, and Zu were mainly from mixed sources, with a considerable portion from anthropogenic activities such as traffic pollutants, domestic garbage, and agricultural inputs, and Hg was mainly from industrial wastes and pollutants.

21 CFR 73.2326 - Chromium hydroxide green.

Code of Federal Regulations, 2010 CFR

2010-04-01

... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Chromium hydroxide green. 73.2326 Section 73.2326 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL LISTING OF... in coloring externally applied cosmetics, including those intended for use in the area of the eye, in...

21 CFR 73.2326 - Chromium hydroxide green.

Code of Federal Regulations, 2011 CFR

2011-04-01

... 21 Food and Drugs 1 2011-04-01 2011-04-01 false Chromium hydroxide green. 73.2326 Section 73.2326 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL LISTING OF... in coloring externally applied cosmetics, including those intended for use in the area of the eye, in...

The effects of organic chromium on adipose anatomical parts, using pig as experimental model.

PubMed

Untea, A E; Varzaru, I; Ropota, M; Panaite, T D; Cornescu, G M

2016-01-01

The aim of this study was to evaluate the influence of chromium supplements on the quality of protein and lipids of adipose anatomical parts using pig as experimental modelfor humans. An experiment was conducted on 18 fattening castrated TOPIGS male pigs, for 4 weeks, under experimental farm conditions. The source of Cr(III) was chromium . picolinate, a food supplement used in human nutrition, 200 µg.Cr per kg diet (El) and 400 µg.Cr per kg diet (E2). The analytic.data showed an improvement of the amino acids profile in belly and in ham samples. A significant decrease of fatty acids concentrations in belly samples was noticed. In conclusion, we observed a positive effect associated with the essential amino acids deposition and decreasing of fatty acids concentrations in tissues with high content offat, thus in human nutrition, chromium is used as a nutritional supplement most recommended in impaired carbohydrate metabolism.

Study on anaerobic treatment of wastewater containing hexavalent chromium.

PubMed

Xu, Yan-bin; Xiao, Hua-hua; Sun, Shui-yu

2005-06-01

A self-made anaerobic bio-filter bed which was inoculated with special sludge showed high efficiency in removing hexavalent chromium. When pump flow was 47 ml/min and COD(Cr) of wastewater was about 140 mg/L, it took 4 h to decrease the Cr6+ concentrations from about 60 mg/L to under 0.5 mg/L, compared with 14 h without carbon source addition. Cr6+ concentrations ranged from 64.66 mg/L to 75.53 mg/L, the system efficiency was excellent. When Cr6+ concentration reached 95.47 mg/L, the treatment time was prolonged to 7.5 h. Compared with the contrast system, the system with trace metals showed clear superiority in that the Cr6+ removal rate increased by 21.26%. Some analyses also showed that hexavalent chromium could probably be bio-reduced to trivalent chromium, and that as a result, the chrome hydroxide sediment was formed on the surface of microorganisms.

Isolation and characterization of Bacillus cereus IST105 from electroplating effluent for detoxification of hexavalent chromium.

PubMed

Naik, Umesh Chandra; Srivastava, Shaili; Thakur, Indu Shekhar

2011-08-01

Electroplating industries are the main sources of heavy metals, chromium, nickel, lead, zinc, cadmium and copper. The highest concentrations of chromium (VI) in the effluent cause a direct hazards to human and animals. Therefore, there is a need of an effective and affordable biotechnological solution for removal of chromium from electroplating effluent. Bacterial strains were isolated from electroplating effluent to find out higher tolerant isolate against chromate. The isolate was identified by 16S rDNA sequence analysis. Absorbed chromium level of bacterium was determined by inductively coupled plasma-atomic emission spectrometer (ICP-AES), atomic absorption spectrophotometer (AAS), scanning electron microscope (SEM), transmission electron microscope (TEM) and energy dispersive X-ray analysis (EDX). Removal of metals by bacterium from the electroplating effluent eventually led to the detoxification of effluent confirmed by MTT assay. Conformational changes of functional groups of bacterial cell surface were studied through Fourier transform infrared spectroscopy. The chromate tolerant isolate was identified as Bacillus cereus. Bacterium has potency to remove more than 75% of chromium as measured by ICP-AES and AAS. The study indicated the accumulation of chromium (VI) on bacterial cell surface which was confirmed by the SEM-EDX and TEM analysis. The biosorption of metals from the electroplating effluent eventually led to the detoxification of effluent. The increased survivability of Huh7 cells cultured with treated effluent also confirmed the detoxification as examined by MTT assay. Isolated strain B. cereus was able to remove and detoxify chromium (VI). It would be an efficient tool of the biotechnological approach in mitigating the heavy metal pollutants.

40 CFR 467.25 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

...) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions... emulsions Chromium 0.057 0.024 Cyanide 0.038 0.016 Zinc 0.190 0.079 TTO 0.090 Oil and grease (alternate...

40 CFR 467.25 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

...) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions... emulsions Chromium 0.057 0.024 Cyanide 0.038 0.016 Zinc 0.190 0.079 TTO 0.090 Oil and grease (alternate...

40 CFR 467.26 - Pretreatment standards for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions Subcategory § 467.26... average mg/off-kg (lb/million off-lbs) of aluminum rolled with emulsions Chromium 0.048 0.020 Cyanide 0...

40 CFR 467.25 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

...) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions... emulsions Chromium 0.057 0.024 Cyanide 0.038 0.016 Zinc 0.190 0.079 TTO 0.090 Oil and grease (alternate...

40 CFR 437.26 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... Recovery § 437.26 Pretreatment standards for new sources (PSNS). Except as provided in 40 CFR 403.7 or...: Standards for chromium, cobalt, copper, lead, tin, zinc, carbazole, n-decane, bis(2-ethylhexyl) phthalate...

40 CFR 437.26 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... Recovery § 437.26 Pretreatment standards for new sources (PSNS). Except as provided in 40 CFR 403.7 or...: Standards for chromium, cobalt, copper, lead, tin, zinc, carbazole, n-decane, bis(2-ethylhexyl) phthalate...

Pretreatment Solution for Water Recovery Systems

NASA Technical Reports Server (NTRS)

Muirhead, Dean (Inventor)

2018-01-01

Chemical pretreatments are used to produce usable water by treating a water source with a chemical pretreatment that contains a hexavalent chromium and an acid to generate a treated water source, wherein the concentration of sulfate compounds in the acid is negligible, and wherein the treated water source remains substantially free of precipitates after the addition of the chemical pretreatment. Other methods include reducing the pH in urine to be distilled for potable water extraction by pretreating the urine before distillation with a pretreatment solution comprising one or more acid sources selected from a group consisting of phosphoric acid, hydrochloric acid, and nitric acid, wherein the urine remains substantially precipitate free after the addition of the pretreatment solution. Another method described comprises a process for reducing precipitation in urine to be processed for water extraction by mixing the urine with a pretreatment solution comprising hexavalent chromium compound and phosphoric acid.

Dietary chromium tripicolinate supplementation reduces glucose concentrations and improves glucose tolerance in normal-weight cats.

PubMed

Appleton, D J; Rand, J S; Sunvold, G D; Priest, J

2002-03-01

The effect of dietary chromium supplementation on glucose and insulin metabolism in healthy, non-obese cats was evaluated. Thirty-two cats were randomly divided into four groups and fed experimental diets consisting of a standard diet with 0 ppb (control), 150 ppb, 300 ppb, or 600 ppb added chromium as chromium tripicolinate. Intravenous glucose tolerance, insulin tolerance and insulin sensitivity tests with minimal model analysis were performed before and after 6 weeks of feeding the test diets. During the glucose tolerance test, glucose concentrations, area under the glucose concentration-time curve, and glucose half-life (300 ppb only), were significantly lower after the trial in cats supplemented with 300 ppb and 600 ppb chromium, compared with values before the trial. Fasting glucose concentrations measured on a different day in the biochemistry profile were also significantly lower after supplementation with 600 ppb chromium. There were no significant differences in insulin concentrations or indices in either the glucose or insulin tolerance tests following chromium supplementation, nor were there any differences between groups before or after the dietary trial.Importantly, this study has shown a small but significant, dose-dependent improvement in glucose tolerance in healthy, non-obese cats supplemented with dietary chromium. Further long-term studies are warranted to determine if the addition of chromium to feline diets is advantageous. Cats most likely to benefit are those with glucose intolerance and insulin resistance from lack of exercise, obesity and old age. Healthy cats at risk of glucose intolerance and diabetes from underlying low insulin sensitivity or genetic factors may also benefit from long-term chromium supplementation. Copyright 2002 ESFM and AAFP.

Impairment of soil health due to fly ash-fugitive dust deposition from coal-fired thermal power plants.

PubMed

Raja, R; Nayak, A K; Shukla, A K; Rao, K S; Gautam, Priyanka; Lal, B; Tripathi, R; Shahid, M; Panda, B B; Kumar, A; Bhattacharyya, P; Bardhan, G; Gupta, S; Patra, D K

2015-11-01

Thermal power stations apart from being source of energy supply are causing soil pollution leading to its degradation in fertility and contamination. Fine particle and trace element emissions from energy production in coal-fired thermal power plants are associated with significant adverse effects on human, animal, and soil health. Contamination of soil with cadmium, nickel, copper, lead, arsenic, chromium, and zinc can be a primary route of human exposure to these potentially toxic elements. The environmental evaluation of surrounding soil of thermal power plants in Odisha may serve a model study to get the insight into hazards they are causing. The study investigates the impact of fly ash-fugitive dust (FAFD) deposition from coal-fired thermal power plant emissions on soil properties including trace element concentration, pH, and soil enzymatic activities. Higher FAFD deposition was found in the close proximity of power plants, which led to high pH and greater accumulation of heavy metals. Among the three power plants, in the vicinity of NALCO, higher concentrations of soil organic carbon and nitrogen was observed whereas, higher phosphorus content was recorded in the proximity of NTPC. Multivariate statistical analysis of different variables and their association indicated that FAFD deposition and soil properties were influenced by the source of emissions and distance from source of emission. Pollution in soil profiles and high risk areas were detected and visualized using surface maps based on Kriging interpolation. The concentrations of chromium and arsenic were higher in the soil where FAFD deposition was more. Observance of relatively high concentration of heavy metals like cadmium, lead, nickel, and arsenic and a low concentration of enzymatic activity in proximity to the emission source indicated a possible link with anthropogenic emissions.

40 CFR 471.73 - New source performance standards (NSPS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... GUIDELINES AND STANDARDS NONFERROUS METALS FORMING AND METAL POWDERS POINT SOURCE CATEGORY Uranium Forming... achieve the following new source performance standards (NSPS). The mass of pollutants in the uranium... mg/off-kg (pounds per million off-pounds) of uranium extruded Cadmium 0.007 0.003 Chromium 0.013 0...

40 CFR 471.73 - New source performance standards (NSPS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... Uranium Forming Subcategory § 471.73 New source performance standards (NSPS). Any new source subject to... in the uranium forming process wastewater shall not exceed the following values: (a) Extrusion spent... monthly average mg/off-kg (pounds per million off-pounds) of uranium extruded Cadmium 0.007 0.003 Chromium...

40 CFR 471.73 - New source performance standards (NSPS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... Uranium Forming Subcategory § 471.73 New source performance standards (NSPS). Any new source subject to... in the uranium forming process wastewater shall not exceed the following values: (a) Extrusion spent... monthly average mg/off-kg (pounds per million off-pounds) of uranium extruded Cadmium 0.007 0.003 Chromium...

40 CFR 471.73 - New source performance standards (NSPS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... Uranium Forming Subcategory § 471.73 New source performance standards (NSPS). Any new source subject to... in the uranium forming process wastewater shall not exceed the following values: (a) Extrusion spent... monthly average mg/off-kg (pounds per million off-pounds) of uranium extruded Cadmium 0.007 0.003 Chromium...

40 CFR 471.73 - New source performance standards (NSPS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... GUIDELINES AND STANDARDS NONFERROUS METALS FORMING AND METAL POWDERS POINT SOURCE CATEGORY Uranium Forming... achieve the following new source performance standards (NSPS). The mass of pollutants in the uranium... mg/off-kg (pounds per million off-pounds) of uranium extruded Cadmium 0.007 0.003 Chromium 0.013 0...

40 CFR 467.65 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

...) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions... drawn with emulsions or soaps Chromium 0.205 0.084 Cyanide 0.135 0.056 Zinc 0.681 0.285 TTO 0.32 Oil and...

40 CFR 467.65 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

...) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions... drawn with emulsions or soaps Chromium 0.205 0.084 Cyanide 0.135 0.056 Zinc 0.681 0.285 TTO 0.32 Oil and...

40 CFR 467.65 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

...) EFFLUENT GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions or Soaps... with emulsions or soaps Chromium 0.205 0.084 Cyanide 0.135 0.056 Zinc 0.681 0.285 TTO 0.32 Oil and...

An outbreak of occupational asthma due to chromium and cobalt.

PubMed

Walters, G I; Moore, V C; Robertson, A S; Burge, C B S G; Vellore, A-D; Burge, P S

2012-10-01

Five metal turners employed by an aerospace manufacturer presented to the Birmingham Chest Clinic occupational lung disease unit. Four cases of occupational asthma (OA) due to chromium salt (3) and cobalt (1) were diagnosed by serial peak-expiratory flow measurements and specific inhalation challenge testing. To measure the extent of the outbreak and to provide epidemiological data to ascertain the aetiology. Participants answered a detailed, self-administered questionnaire, designed to detect occupational lung disease. Urine chromium and cobalt excretion, spirometry and exhaled nitric oxide measurements were taken. Those with possible, probable or definite non-OA or OA, after questionnaire, were invited to undertake two-hourly peak flow measurements and received specialist follow-up. A total of 62 workers (95% of workforce) participated. Sixty-one per cent of employees were working in higher metalworking fluid (MWF) exposure areas. Ninety per cent of workers had urinary chromium excretion indicating occupational exposure. Sixty-six per cent of workers reported active respiratory symptoms, although there were no significant differences between exposure groups. Two further workers with probable OA were identified and had significantly higher urinary chromium and cobalt concentration than asymptomatic controls. Eighteen cases of occupational rhinitis (OR) were identified, with significantly raised urinary chromium concentration compared with asymptomatic controls. Chromium salt and cobalt can be responsible for OA and OR in workers exposed to MWF aerosols. Onset of symptoms in those with positive specific challenges followed change in MWF brand. Workers with OA had increased urinary concentrations of chromium and cobalt, and those with OR had increased urinary concentrations of chromium.

Ecophysiological responses of young mangrove species Rhizophora apiculata (Blume) to different chromium contaminated environments.

PubMed

Nguyen, Kim Linh; Nguyen, Hoang Anh; Richter, Otto; Pham, Minh Thinh; Nguyen, Van Phuoc

2017-01-01

Many mangrove forests have suffered from the contaminated environments near industrial areas. This study addresses the question how these environments influence the renewal of mangrove forests. To this end ecophysiological responses of the young mangrove species Rhizophora apiculata (Blume) grown under combinations of the factors heavy metals (here chromium), nutrition and soil/water environment were analyzed. We tested the hypothesis that soil/water conditions and nutrient status of the soil strongly influence the toxic effect of chromium. Seedlings of R. apiculata were grown in three different soil/water environments (natural saline soil with brackish water, salt-leached soil with fresh water and salt-leached-sterilized soil with fresh water) treated with different levels of chromium and NPK fertilizer. The system was inundated twice a day as similar to natural tidal condition in the mangrove wetland in the south of Vietnam. The experiments were carried out for 6months. Growth data of root, leaf and stem, root cell number and stomata number were recorded and analyzed. Results showed that growth of R. apiculata is slower in natural saline soil/water condition. The effect of chromium and of nutrients respectively depends on the soil/water condition. Under high concentrations of chromium, NPK fertilizer amplifies the toxic effect of chromium. Stomata density increases under chromium stress and is largest under the combination of chromium and salty soil/water condition. From the data a nonlinear multivariate regression model was derived capturing the toxicity threshold of R. apiculata under different treatment combinations. Copyright © 2016 Elsevier B.V. All rights reserved.

Metals distribution in soils around the cement factory in southern Jordan.

PubMed

Al-Khashman, Omar A; Shawabkeh, Reyad A

2006-04-01

Thirty one soil samples were collected from south Jordan around the cement factory in Qadissiya area. The samples were obtained at two depths, 0-10 cm and 10-20 cm and were analyzed by atomic absorption spectrophotometery for Pb, Zn, Cd, Fe, Cu and Cr. Physicochemical factors believed to affect their mobility of metals in soil of the study area were examined such as; pH, TOM, CaCO3, CEC and conductivity. The relatively high concentrations of lead, zinc and cadmium in the soil samples of the investigated area were related to anthropogenic sources such as cement industry, agriculture activities and traffic emissions. It was found that the lead, zinc and cadmium have the highest level in area close to the cement factory, while the concentration of chromium was low. This study indicate that all of the metals are concentrated on the surface soil, and decreased in the lower part of the soil, this due to reflects their mobility and physical properties of soil and its alkaline pH values. The use of factor analysis showed that anthropogenic activities seem to be the responsible source of pollution for metals in urban soils.

40 CFR 437.25 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2011 CFR

2011-07-01

... Recovery § 437.25 Pretreatment standards for existing sources (PSES). Except as provided in 40 CFR 403.7...) Regulatedparameter Maximum daily 1 Maximum monthly avg. 1 Metal Parameters Chromium 0.947 0.487 Cobalt 56.4 18.8...

40 CFR 437.25 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2010 CFR

2010-07-01

... Recovery § 437.25 Pretreatment standards for existing sources (PSES). Except as provided in 40 CFR 403.7...) Regulatedparameter Maximum daily 1 Maximum monthly avg. 1 Metal Parameters Chromium 0.947 0.487 Cobalt 56.4 18.8...

NAVAIR Progress in Assessing, Validating and Implementing Non-Chromate Primers (Briefing charts)

DTIC Science & Technology

2011-02-09

logistics for any new coating or coating system NAVAIR Application Areas for Hexavalent Chromium Alternatives: Status Components/ Structure... Hexavalent chromium alternatives Sacrificial Coating Post Treatment MIL-A-8625 Anodize Avionics/ Electronics Magnesium/Titanium Conversion Aluminum Anodizing...Aluminum Pretreatment Type IC Seal Type IIB Seal Type II Seal Phosphating Rinse (Aluminum)Rinse (Steel) Cadmium Zinc-Nickel Aluminum Bonding Chrome

The use of bio-monitoring to assess exposure in the electroplating industry

PubMed Central

Beattie, Helen; Keen, Chris; Coldwell, Matthew; Tan, Emma; Morton, Jackie; McAlinden, John; Smith, Paul

2017-01-01

Workers in the electroplating industry are potentially exposed to a range of hazardous substances including nickel and hexavalent chromium (chromium VI) compounds. These can cause serious health effects, including cancer, asthma and dermatitis. This research aimed to investigate whether repeat biological monitoring (BM) over time could drive sustainable improvements in exposure control in the industry. BM was performed on multiple occasions over 3 years, at 53 electroplating companies in Great Britain. Surface and dermal contamination was also measured, and controls were assessed. Air monitoring was undertaken on repeat visits where previous BM results were of concern. There were significant reductions in urinary nickel and chromium levels over the lifetime of this work in the subset of companies where initially, control deficiencies were more significant. Increased risk awareness following provision of direct feedback to individual workers and targeted advice to companies is likely to have contributed to these reductions. This study has shown that exposures to chromium VI and nickel in the electroplating industry occur via a combination of inhalation, dermal and ingestion routes. Surface contamination found in areas such as canteens highlights the potential for transferral from work areas, and the importance of a regular cleaning regime. PMID:26627055

The use of bio-monitoring to assess exposure in the electroplating industry.

PubMed

Beattie, Helen; Keen, Chris; Coldwell, Matthew; Tan, Emma; Morton, Jackie; McAlinden, John; Smith, Paul

2017-01-01

Workers in the electroplating industry are potentially exposed to a range of hazardous substances including nickel and hexavalent chromium (chromium VI) compounds. These can cause serious health effects, including cancer, asthma and dermatitis. This research aimed to investigate whether repeat biological monitoring (BM) over time could drive sustainable improvements in exposure control in the industry. BM was performed on multiple occasions over 3 years, at 53 electroplating companies in Great Britain. Surface and dermal contamination was also measured, and controls were assessed. Air monitoring was undertaken on repeat visits where previous BM results were of concern. There were significant reductions in urinary nickel and chromium levels over the lifetime of this work in the subset of companies where initially, control deficiencies were more significant. Increased risk awareness following provision of direct feedback to individual workers and targeted advice to companies is likely to have contributed to these reductions. This study has shown that exposures to chromium VI and nickel in the electroplating industry occur via a combination of inhalation, dermal and ingestion routes. Surface contamination found in areas such as canteens highlights the potential for transferral from work areas, and the importance of a regular cleaning regime.

Optical and spectroscopic studies on tannery wastes as a possible source of organic semiconductors

NASA Astrophysics Data System (ADS)

Nashy, El-Shahat H. A.; Al-Ashkar, Emad; Abdel Moez, A.

2012-02-01

Tanning industry produces a large quantity of solid wastes which contain hide proteins in the form of protein shavings containing chromium salts. The chromium wastes are the main concern from an environmental stand point of view, because chrome wastes posses a significant disposal problem. The present work is devoted to investigate the possibility of utilizing these wastes as a source of organic semi-conductors as an alternative method instead of the conventional ones. The chemical characterization of these wastes was determined. In addition, the Horizontal Attenuated Total Reflection (HATR) FT-IR spectroscopic analysis and optical parameters were also carried out for chromated samples. The study showed that the chromated samples had suitable absorbance and transmittance in the wavelength range (500-850 nm). Presence of chromium salt in the collagen samples increases the absorbance which improves the optical properties of the studied samples and leads to decrease the optical energy gap. The obtained optical energy gap gives an impression that the environmentally hazardous chrome shavings wastes can be utilized as a possible source of natural organic semiconductors with direct and indirect energy gap. This work opens the door to use some hazardous wastes in the manufacture of electronic devices such as IR-detectors, solar cells and also as solar cell windows.

Assessment of skin exposure to nickel, chromium and cobalt by acid wipe sampling and ICP-MS.

PubMed

Lidén, Carola; Skare, Lizbet; Lind, Birger; Nise, Gun; Vahter, Marie

2006-05-01

There is a great need to accurately assess skin exposure to contact allergens. We have developed a technique for assessment of skin exposure to nickel, chromium and cobalt using acid wipe sampling by cellulose wipes with 1% nitric acid. Chemical analysis was performed by inductively coupled plasma mass spectrometry (ICP-MS). The recovery of nickel, chromium and cobalt from arms and palms was 93%. The analytical result is expressed in terms of mass per unit area (microg/cm(2)). The developed acid wipe sampling technique is suitable for determination of nickel, chromium and cobalt deposited on the skin. The technique may be used in workplace studies, in studies of individuals in the general population, in dermatitis patients, in identification of risk groups, as well as in developing preventive strategies and in follow-up after intervention.

X-ray Absorption and Emission Spectroscopy of CrIII (Hydr)Oxides: Analysis of the K-Pre-Edge Region

NASA Astrophysics Data System (ADS)

Frommer, Jakob; Nachtegaal, Maarten; Czekaj, Izabela; Weng, Tsu-Chien; Kretzschmar, Ruben

2009-10-01

Pre-edge spectral features below the main X-ray absorption K-edge of transition metals show a pronounced chemical sensitivity and are promising sources of structural information. Nevertheless, the use of pre-edge analysis in applied research is limited because of the lack of definite theoretical peak-assignments. The aim of this study was to determine the factors affecting the chromium K-pre-edge features in trivalent chromium-bearing oxides and oxyhydroxides. The selected phases varied in the degree of octahedral polymerization and the degree of iron-for-chromium substitution in the crystal structure. We investigated the pre-edge fine structure by means of high-energy-resolution fluorescence detected X-ray absorption spectroscopy and by 1s2p resonant X-ray emission spectroscopy. Multiplet theory and full multiple-scattering calculations were used to analyze the experimental data. We show that the chromium K-pre-edge contains localized and nonlocalized transitions. Contributions arising from nonlocalized metal-metal transitions are sensitive to the nearest metal type and to the linkage mode between neighboring metal octahedra. Analyzing these transitions opens up new opportunities for investigating the local coordination environment of chromium in poorly ordered solids of environmental relevance.

40 CFR 471.75 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... CATEGORY Uranium Forming Subcategory § 471.75 Pretreatment standards for new sources (PSNS). Except as... standards for new sources (PSNS). The mass of wastewater pollutants in uranium forming process wastewater... (pounds per million off-pounds) of uranium extruded Cadmium 0.007 0.003 Chromium 0.013 0.005 Copper 0.044...

40 CFR 471.75 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... CATEGORY Uranium Forming Subcategory § 471.75 Pretreatment standards for new sources (PSNS). Except as... standards for new sources (PSNS). The mass of wastewater pollutants in uranium forming process wastewater... (pounds per million off-pounds) of uranium extruded Cadmium 0.007 0.003 Chromium 0.013 0.005 Copper 0.044...

40 CFR 471.75 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... CATEGORY Uranium Forming Subcategory § 471.75 Pretreatment standards for new sources (PSNS). Except as... standards for new sources (PSNS). The mass of wastewater pollutants in uranium forming process wastewater... (pounds per million off-pounds) of uranium extruded Cadmium 0.007 0.003 Chromium 0.013 0.005 Copper 0.044...

40 CFR 461.75 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

...) EFFLUENT GUIDELINES AND STANDARDS BATTERY MANUFACTURING POINT SOURCE CATEGORY Zinc Subcategory § 461.75... and achieve the following pretreatment standards for new sources listed below: (1) Subpart G—Zinc... average Metric units—mg/kg of zinc English units—pounds per 1,000,000 pounds of zinc Chromium 4.55 1.97...

Effects of Supplemental Chromium Source and Concentration on Growth, Carcass Characteristics, and Serum Lipid Parameters of Broilers Reared Under Normal Conditions.

PubMed

Zheng, Cancai; Huang, Yanling; Xiao, Fang; Lin, Xi; Lloyd, Karen

2016-02-01

An experiment was conducted to investigate the effects of dietary chromium (Cr) source and concentration on growth performance, carcass traits, and some serum lipid parameters of broilers under normal rearing conditions for 42 days. A total of 252 1-day-old Cobb 500 commercial female broilers were randomly allotted by body weight (BW) to one of six replicate cages (six broilers per cage) for each of seven treatments in a completely randomized design involved in a 2 × 3 factorial arrangement of treatments with three Cr sources (Cr propionate (CrPro), Cr picolinate (CrPic), Cr chloride (CrCl3)) and two concentrations of added Cr (0.4 and 2.0 mg of Cr/kg) plus a Cr-unsupplemented control diet. The results showed that dietary Cr supplementation tended to increase the breast muscle percentage compared with the Cr-unsupplemented control group (P = 0.0784), while Cr from CrPic tended to have higher breast muscle percentage compared with Cr from CrCl3 (P = 0.0881). Chromium from CrPic also tended to increase the breast intramuscular fat (IMF) compared with Cr from CrCl3 (P = 0.0648). In addition, supplementation of 0.4 mg/kg Cr tended to decrease low-density lipoprotein cholesterol (LDL-C) (P = 0.0614). Compared with the control group, broilers fed Cr-supplemented diets had higher triglyceride (TG) (P = 0.0129) regardless of Cr source and Cr concentration. Chromium from CrPro and CrPic had lower total cholesterol (TC) compared with Cr from CrCl3 (P = 0.0220). These results indicate that dietary supplementation of Cr has effects on carcass characteristics and serum lipid parameters of broilers under normal rearing conditions, while supplementation of organic Cr can improve carcass characteristics and reduce the cholesterol content in serum.

Study on anaerobic treatment of wastewater containing hexavalent chromium*

PubMed Central

Xu, Yan-bin; Xiao, Hua-hua; Sun, Shui-yu

2005-01-01

A self-made anaerobic bio-filter bed which was inoculated with special sludge showed high efficiency in removing hexavalent chromium. When pump flow was 47 ml/min and CODCr of wastewater was about 140 mg/L, it took 4 h to decrease the Cr6+ concentrations from about 60 mg/L to under 0.5 mg/L, compared with 14 h without carbon source addition. Cr6+ concentrations ranged from 64.66 mg/L to 75.53 mg/L, the system efficiency was excellent. When Cr6+ concentration reached 95.47 mg/L, the treatment time was prolonged to 7.5 h. Compared with the contrast system, the system with trace metals showed clear superiority in that the Cr6+ removal rate increased by 21.26%. Some analyses also showed that hexavalent chromium could probably be bio-reduced to trivalent chromium, and that as a result, the chrome hydroxide sediment was formed on the surface of microorganisms. PMID:15909347

Amino acid, mineral and fatty acid content of pumpkin seeds (Cucurbita spp) and Cyperus esculentus nuts in the Republic of Niger.

PubMed

Glew, R H; Glew, R S; Chuang, L-T; Huang, Y-S; Millson, M; Constans, D; Vanderjagt, D J

2006-06-01

Dried seeds and nuts are widely consumed by indigenous populations of the western Sahel, especially those who inhabit rural areas. In light of the need for quantitative information regarding the content of particular nutrients in these plant foods, we collected dried pumpkin (Cucurbita spp) seeds and nuts of Cyperus esculentus in the Republic of Niger and analyzed them for their content of essential amino acids, minerals and trace elements, and fatty acids. On a dry weight basis, pumpkin seed contained 58.8% protein and 29.8% fat. However, the lysine score of the protein was only 65% relative to the FAO/WHO protein standard. The pumpkin seed contained useful amounts of linoleic (92 microg/g dry weight) and the following elements (on a microg per g dry weight basis): potassium (5,790), magnesium (5,690), manganese (49.3), zinc (113), selenium (1.29), copper (15.4), chromium (2.84), and molybdenum (0.81), but low amounts of calcium and iron. Except for potassium (5,573 microg/g dry weight) and chromium (2.88 microg/g dry weight), the C. esculentis nuts contained much less of these same nutrients compared to pumpkin seeds. In conclusion, pumpkin seeds represent a useful source of many nutrients essential to humans. The data in this report should of practical value to public health officials in rural areas of sub-Saharan Africa.

40 CFR 467.65 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

... or Soaps Subcategory § 467.65 Pretreatment standards for existing sources. Except as provided in 40... drawn with emulsions or soaps Chromium 0.205 0.084 Cyanide 0.135 0.056 Zinc 0.681 0.285 TTO 0.32 Oil and...

Determination of heavy metals in the ambient atmosphere.

PubMed

Suvarapu, Lakshmi Narayana; Baek, Sung-Ok

2017-01-01

Heavy metal determination in ambient air is an important task for environmental researchers because of their toxicity to human beings. Some heavy metals (hexavalent chromium (Cr), arsenic (As), cadmium (Cd) and nickel (Ni)) have been listed as carcinogens. Furthermore, heavy metals in the atmosphere can accumulate in various plants and animals and enter humans through the food chain. This article reviews the determination of heavy metals in the atmosphere in different areas of the world since 2006. The results showed that most researchers concentrated on toxic metals, such as Cr, Cd, Ni, As and lead. A few studies used plant materials as bio-monitors for the atmospheric levels of heavy metals. Some researchers found higher concentrations of heavy metals surrounding industrial areas compared with residential and/or commercial areas. Most studies reported the major sources of the particulate matter and heavy metals in the atmosphere to be industrial emissions, vehicular emissions and secondary aerosols.

Heat Source - Materials Interactions during Fusion Welding.

DTIC Science & Technology

1982-04-30

calcium, chromium and tungsten lines have been identified. In the titanium spectra (Figure 6), argon, titanium, aluminum, calcium and tungsten lines have...Stainless Steel," Weld J.,5(12), 1974, p. 5 4 9 -r. 3. C. B. Shaw, Jr. "Diagnostic Studies of the GTAW Arc," Weld J. 54(2), p.33-s. 4. J. F. Key, M. E...black body radiation curve. The diagram is valid only in the manganese m.p.-b.p. range. Fig.-8 Chromium isopleths plotted against log of pressure, log

Sources, spatial variation, and speciation of heavy metals in sediments of the Tamagawa River in Central Japan.

PubMed

Shikazono, N; Tatewaki, K; Mohiuddin, K M; Nakano, T; Zakir, H M

2012-01-01

Sediments of the Tamagawa River in central Japan were studied to explain the spatial variation, to identify the sources of heavy metals, and to evaluate the anthropogenic influence on these pollutants in the river. Sediment samples were collected from 20 sites along the river (five upstream, four midstream, and 11 downstream). Heavy metal concentrations, viz. chromium, nickel, copper, zinc, lead, cadmium, and molybdenum, in the samples were measured using inductively coupled plasma-mass spectroscopy. The chemical speciations of heavy metals in the sediments were identified by the widely used five-step Hall method. Lead isotopes were analyzed to identify what portion is contributed by anthropogenic sources. The total heavy metal concentrations were compared with global averages for continental crust (shale) and average values for Japanese river sediments. The mean heavy metal concentrations were higher in downstream sediments than in upstream and midstream samples, and the concentrations in the silt samples were higher than those in the sand samples. Speciation results demonstrate that, for chromium and nickel, the residual fractions were dominant. These findings imply that the influence of anthropogenic chromium and nickel contamination is negligible, while copper, zinc, and lead were mostly extracted in the non-residual fraction (metals in adsorbed/exchangeable/carbonate forms or bound to amorphous Fe oxyhydroxides, crystalline Fe oxides, or organic matter), indicating that these elements have high chemical mobility. The proportion of lead (Pb) isotopes in the downstream silt samples indicates that Pb accumulation is primarily derived from anthropogenic sources.

Origin of hexavalent chromium in groundwater: The example of Sarigkiol Basin, Northern Greece.

PubMed

Kazakis, N; Kantiranis, N; Kalaitzidou, K; Kaprara, E; Mitrakas, M; Frei, R; Vargemezis, G; Tsourlos, P; Zouboulis, A; Filippidis, A

2017-09-01

Hexavalent chromium constitutes a serious deterioration factor for the groundwater quality of several regions around the world. High concentrations of this contaminant have been also reported in the groundwater of the Sarigkiol hydrological basin (near Kozani city, NW Greece). Specific interest was paid to this particular study area due to the co-existence here of two important factors both expected to contribute to Cr(VI) presence and groundwater pollution; namely the area's exposed ophiolitic rocks and its substantial fly ash deposits originating from the local lignite burning power plant. Accordingly, detailed geochemical, mineralogical, hydro-chemical, geophysical and hydrogeological studies were performed on the rocks, soils, sediments and water resources of this basin. Cr(VI) concentrations varied in the different aquifers, with the highest concentration (up to 120μgL -1 ) recorded in the groundwater of the unconfined porous aquifer situated near the temporary fly ash disposal site. Recharge of the porous aquifer is related mainly to precipitation infiltration and occasional surface run-off. Nevertheless, a hydraulic connection between the porous and neighboring karst aquifers could not be delineated. Therefore, the presence of Cr(VI) in the groundwater of this area is thought to originate from both the ophiolitic rock weathering products in the soils, and the local leaching of Cr(VI) from the diffused fly ash located in the area surrounding the lignite power plant. This conclusion was corroborated by factor analysis, and the strongly positively fractionated Cr isotopes (δ 53 Cr up to 0.83‰) recorded in groundwater, an ash leachate, and the bulk fly ash. An anthropogenic source of Cr(VI) that possibly influences groundwater quality is especially apparent in the eastern part of the Sarigkiol basin. Copyright © 2017 Elsevier B.V. All rights reserved.

Assessment of Hexavalent Chromium Natural Attenuation for the Hanford Site 100 Area

DOE Office of Scientific and Technical Information (OSTI.GOV)

Truex, Michael J.; Szecsody, James E.; Qafoku, Nikolla P.

2015-09-01

Hexavalent chromium (Cr(VI)) plumes are present in the 100 Area at the Hanford Site. Remediation efforts are under way with objectives of restoring the groundwater to meet the drinking-water standard (48 µg/L) and protecting the Columbia River by ensuring that discharge of groundwater to the river is below the surface-water quality standard (10 µg/L). Current remedies include application of Pump-and-Treat (P&T) at the 100-D, 100-H, and 100-K Areas and Monitored Natural Attenuation (MNA) at the 100-F/IU Area. Remedy selection is still under way at the other 100 Areas. Additional information about the natural attenuation processes for Cr(VI) is important inmore » all of these cases. In this study, laboratory experiments were conducted to demonstrate and quantify natural attenuation mechanisms using 100 Area sediments and groundwater conditions.« less

An assessment of hematological and biochemical responses in the tropical fish Epinephelus stoliczkae of Chabahar Bay and Gulf of Oman under chromium exposure: ecological and experimental tests.

PubMed

Sadeghi, Parvin; Savari, Ahmad; Movahedinia, Abdolali; Safahieh, Alireza; Azhdari, Danial

2014-05-01

The aim of this investigation was to evaluate the effect of chromium on hematological and biochemical parameters in Epaulet Grouper, Epinephelus stoliczkae of Chabahar Bay and Gulf of Oman by ecological and experimental tests. Spatial evaluation of ecological test results showed these parameters had significant difference among some sampling sites. Examination of hematological and biochemical profiles on Epaulet Grouper was performed after 0.5, 1, 7, 14, and 21 days of chromium exposure (3.6, 7.31 and 14.6 mg/L). Experimental test results of chromium induce indicated the significant decrease in MCV, MCH, neutrophils, basophils, plasma protein and significant increase in MCHC, lymphocytes, monocytes, eosinophils and a biphasic trend in Hb, Ht, RBC, WBC, and glucose (p < 0.05). Cellular and nuclear axis, cytoplasmic volume, cell and nuclear volume, and surface area were significantly different for ecological and experimental results (p < 0.05). It was concluded that these parameters are sensitive in monitoring the toxicity of chromium concentrations.

Heavy metals in soil at a waste electrical and electronic equipment processing area in China.

PubMed

Gu, Weihua; Bai, Jianfeng; Yao, Haiyan; Zhao, Jing; Zhuang, Xuning; Huang, Qing; Zhang, Chenglong; Wang, JingWei

2017-11-01

For the objective of evaluating the contamination degree of heavy metals and analysing its variation trend in soil at a waste electrical and electronic equipment processing area in Shanghai, China, evaluation methods, which include single factor index method, geo-accumulation index method, comprehensive pollution index method, and potential ecological risk index method, were adopted in this study. The results revealed that the soil at a waste electrical and electronic equipment processing area was polluted by arsenic, cadmium, copper, lead, zinc, and chromium. It also demonstrated that the concentrations of heavy metals were increased over time. Exceptionally, the average value of the metalloid (arsenic) was 73.31 mg kg -1 in 2014, while it was 58.31 mg kg -1 in the first half of 2015, and it was 2.93 times and 2.33 times higher than that of the Chinese Environmental Quality Standard for Soil in 2014 and the first half of 2015, respectively. The sequences of the contamination degree of heavy metals in 2014 and the first half of 2015 were cadmium > lead > copper > chromium > zinc and cadmium > lead > chromium > zinc > copper. From the analysis of the potential ecological risk index method, arsenic and cadmium had higher ecological risk than other heavy metals. The integrated ecological risk index of heavy metals (cadmium, copper, lead, zinc, and chromium) and metalloid (arsenic) was 394.10 in 2014, while it was 656.16 in the first half of 2015, thus documenting a strong ecological risk.

40 CFR 421.304 - Standards of performance for new sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

... Secondary Titanium Subcategory § 421.304 Standards of performance for new sources. Any new source subject to... air pollution control. NSPS Limitations for the Primary and Secondary Titanium Subcategory Pollutant... pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496...

40 CFR 421.304 - Standards of performance for new sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

... Secondary Titanium Subcategory § 421.304 Standards of performance for new sources. Any new source subject to... air pollution control. NSPS Limitations for the Primary and Secondary Titanium Subcategory Pollutant... pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496...

40 CFR 421.304 - Standards of performance for new sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

... Secondary Titanium Subcategory § 421.304 Standards of performance for new sources. Any new source subject to... air pollution control. NSPS Limitations for the Primary and Secondary Titanium Subcategory Pollutant... pounds) of TiCl4 produced Chromium (total) 0.346 0.140 Lead 0.262 0.122 Nickel 0.515 0.346 Titanium 0.496...

40 CFR 63.11602 - What are the performance test and compliance requirements for new and existing sources?

Code of Federal Regulations, 2013 CFR

2013-07-01

... compliance requirements for new and existing sources? 63.11602 Section 63.11602 Protection of Environment... Requirements § 63.11602 What are the performance test and compliance requirements for new and existing sources... compounds of cadmium, chromium, lead, or nickel to a process vessel or to the grinding and milling equipment...

40 CFR 63.11602 - What are the performance test and compliance requirements for new and existing sources?

Code of Federal Regulations, 2012 CFR

2012-07-01

... compliance requirements for new and existing sources? 63.11602 Section 63.11602 Protection of Environment... Requirements § 63.11602 What are the performance test and compliance requirements for new and existing sources... compounds of cadmium, chromium, lead, or nickel to a process vessel or to the grinding and milling equipment...

40 CFR 63.11602 - What are the performance test and compliance requirements for new and existing sources?

Code of Federal Regulations, 2010 CFR

2010-07-01

... compliance requirements for new and existing sources? 63.11602 Section 63.11602 Protection of Environment... Requirements § 63.11602 What are the performance test and compliance requirements for new and existing sources... compounds of cadmium, chromium, lead, or nickel to a process vessel or to the grinding and milling equipment...

40 CFR 63.11602 - What are the performance test and compliance requirements for new and existing sources?

Code of Federal Regulations, 2014 CFR

2014-07-01

... compliance requirements for new and existing sources? 63.11602 Section 63.11602 Protection of Environment... Requirements § 63.11602 What are the performance test and compliance requirements for new and existing sources... compounds of cadmium, chromium, lead, or nickel to a process vessel or to the grinding and milling equipment...

40 CFR 63.11602 - What are the performance test and compliance requirements for new and existing sources?

Code of Federal Regulations, 2011 CFR

2011-07-01

... compliance requirements for new and existing sources? 63.11602 Section 63.11602 Protection of Environment... Requirements § 63.11602 What are the performance test and compliance requirements for new and existing sources... compounds of cadmium, chromium, lead, or nickel to a process vessel or to the grinding and milling equipment...

Chemical-specific health consultation for chromated copper arsenate chemical mixture: port of Djibouti.

PubMed

Chou, Selene; Colman, Joan; Tylenda, Carolyn; De Rosa, Christopher

2007-05-01

The Agency for Toxic Substances and Disease Registry (ATSDR) prepared this health consultation to provide support for assessing the public health implications of hazardous chemical exposure, primarily through drinking water, related to releases of chromated copper arsenate (CCA) in the port of Djibouti. CCA from a shipment, apparently intended for treating electric poles, is leaking into the soil in the port area. CCA is a pesticide used to protect wood against decay-causing organisms. This mixture commonly contains chromium(VI) (hexavalent chromium) as chromic acid, arsenic(V) (pentavalent arsenic) as arsenic pentoxide and copper (II) (divalent copper) as cupric oxide, often in an aqueous solution or concentrate. Experimental studies of the fate of CCA in soil and monitoring studies of wood-preserving sites where CCA was spilled on the soil indicate that the chromium(VI), arsenic and copper components of CCA can leach from soil into groundwater and surface water. In addition, at CCA wood-preserving sites, substantial concentrations of chromium(VI), arsenic and copper remained in the soil and were leachable into water four years after the use of CCA was discontinued, suggesting prolonged persistence in soil, with continued potential for leaching. The degree of leaching depended on soil composition and the extent of soil contamination with CCA. In general, leaching was highest for chromium(VI), intermediate for arsenic and lowest for copper. Thus, the potential for contamination of sources of drinking water exists. Although arsenic that is leached from CCA-contaminated soil into surface water may accumulate in the tissues of fish and shellfish, most of the arsenic in these animals will be in a form (often called fish arsenic) that is less harmful. Copper, which leaches less readily than the other components, can accumulate in tissues of mussels and oysters. Chromium is not likely to accumulate in the tissues of fish and shellfish. Limited studies of air concentrations during cleanup of CCA-contaminated soil at wood- preserving sites showed that air levels of chromium(VI), arsenic and copper were below the occupational standards. Workers directly involved in the repackaging, containment or cleanup of leaking containers of CCA or of soil saturated with CCA, however, may be exposed to high levels of CCA through direct dermal contact, inhalation of aerosols or particulates and inadvertent ingestion. Few studies have been conducted on the health effects of CCA. CCA as a concentrated solution is corrosive to the skin eyes and digestive tract. Studies of workers exposed to CCA in wood-preserving plants have not found adverse health effects in these workers, but the studies involved small numbers of workers and therefore are not definitive. People exposed to very high levels of CCA, from sawing wood that still had liquid CCA in it or from living in a home contaminated with ash containing high levels of chromium(VI), arsenic and copper, experienced serious health effects including nosebleeds, digestive system pain and bleeding, itching skin, darkened urine, nervous system effects such as tingling or numbness of the hands and feet and confusion, and rashes or thickening and peeling of the skin. These health effects of the mixture are at least qualitatively reflective of the health effects of the individual components of CCA (arsenic, chromium(VI) and copper). For a given mixture, the critical effects of the individual components are of particular concern, as are any effects in common that may become significant due to additivity or interactions among the components. Effects of concern for CCA, based on the known effects of the individual components, include cancer (arsenic by the oral route, arsenic and chromium(VI) by the inhalation route), irritant or corrosive effects (all three mixture components), the unique dermal effects of arsenic, neurologic effects (arsenic and chromium(VI), and hematologic, hepatic and renal effects (all three components). Because arsenic, chromium(VI), and copper components affect some of the same target organs, they may have additive toxicity toward those organs. Few studies have investigated the potential toxic interactions among the components (arsenic, chromium(VI) and copper) of CCA. The available interaction studies and also possible mechanisms of interaction were evaluated using a weight-of-evidence approach. The conclusion is that there is no strong evidence that interactions among the components of CCA will result in a marked increase in toxicity. This conclusion reflects a lack of well designed interaction studies as well as uncertainties regarding potential mechanisms of interaction. Confidence in the conclusion is low. Workers exposed to high levels of CCA during cleanup of leaking containers of CCA or soil heavily contaminated with CCA should wear protective clothing and respirators if air concentrations of arsenic are above 10 microg/m3. In addition, they should not eat, drink or use tobacco products during exposure to CCA, and should thoroughly wash after skin contact with CCA and before eating, drinking, using tobacco products or using restrooms. When protective clothing becomes contaminated with CCA, it should be changed, and the contaminated clothing should be disposed off in a manner approved for pesticide disposal. Workers should leave all protective clothing, including work shoes and boots, at the workplace, so that CCA will not be carried into their cars and homes, which would endanger other people. People not involved in the cleanup of the CCA and who are not wearing protective clothing should be prevented from entering contaminated areas. Leaking containers of CCA must be repackaged and contained to prevent direct exposure of on-site personnel; and contaminated soil needs to be removed to prevent the CCA from leaching into surface water and groundwater, thereby contaminating sources of drinking water.

40 CFR 421.324 - Standards of performance for new sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

...) EFFLUENT GUIDELINES AND STANDARDS NONFERROUS METALS MANUFACTURING POINT SOURCE CATEGORY Secondary Uranium... Uranium Subcategory Pollutant or pollutant property Maximum for any 1 day Maximum for monthly average mg/kg (pounds per million pounds) of uranium processed in the refinery Chromium (total) 27.14 11.00...

40 CFR 421.324 - Standards of performance for new sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

...) EFFLUENT GUIDELINES AND STANDARDS NONFERROUS METALS MANUFACTURING POINT SOURCE CATEGORY Secondary Uranium... Uranium Subcategory Pollutant or pollutant property Maximum for any 1 day Maximum for monthly average mg/kg (pounds per million pounds) of uranium processed in the refinery Chromium (total) 27.14 11.00...

40 CFR 421.324 - Standards of performance for new sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

...) EFFLUENT GUIDELINES AND STANDARDS NONFERROUS METALS MANUFACTURING POINT SOURCE CATEGORY Secondary Uranium... Uranium Subcategory Pollutant or pollutant property Maximum for any 1 day Maximum for monthly average mg/kg (pounds per million pounds) of uranium processed in the refinery Chromium (total) 27.14 11.00...

Stainless steel leaches nickel and chromium into foods during cooking.

PubMed

Kamerud, Kristin L; Hobbie, Kevin A; Anderson, Kim A

2013-10-02

Toxicological studies show that oral doses of nickel and chromium can cause cutaneous adverse reactions such as dermatitis. Additional dietary sources, such as leaching from stainless steel cookware during food preparation, are not well characterized. This study examined stainless steel grades, cooking time, repetitive cooking cycles, and multiple types of tomato sauces for their effects on nickel and chromium leaching. Trials included three types of stainless steels and a stainless steel saucepan, cooking times of 2-20 h, 10 consecutive cooking cycles, and four commercial tomato sauces. After a simulated cooking process, samples were analyzed by ICP-MS for Ni and Cr. After 6 h of cooking, Ni and Cr concentrations in tomato sauce increased up to 26- and 7-fold, respectively, depending on the grade of stainless steel. Longer cooking durations resulted in additional increases in metal leaching, where Ni concentrations increased 34-fold and Cr increased approximately 35-fold from sauces cooked without stainless steel. Cooking with new stainless steel resulted in the largest increases. Metal leaching decreases with sequential cooking cycles and stabilized after the sixth cooking cycle, although significant metal contributions to foods were still observed. The tenth cooking cycle resulted in an average of 88 μg of Ni and 86 μg of Cr leached per 126 g serving of tomato sauce. Stainless steel cookware can be an overlooked source of nickel and chromium, where the contribution is dependent on stainless steel grade, cooking time, and cookware usage.

Stainless Steel Leaches Nickel and Chromium into Foods During Cooking

PubMed Central

Kamerud, Kristin L.; Hobbie, Kevin A.; Anderson, Kim A.

2014-01-01

Toxicological studies show that oral doses of nickel and chromium can cause cutaneous adverse reactions such as dermatitis. Additional dietary sources, such as leaching from stainless steel cookware during food preparation, are not well characterized. This study examined stainless steel grades, cooking time, repetitive cooking cycles, and multiple types of tomato sauces for their effects on nickel and chromium leaching. Trials included three types of stainless steels and a stainless steel saucepan; cooking times of 2 to 20 hours, ten consecutive cooking cycles, and four commercial tomato sauces. After a simulated cooking process, samples were analyzed by ICP-MS for Ni and Cr. After six hours of cooking, Ni and Cr concentrations in tomato sauce increased up to 26- and 7-fold respectively, depending on the grade of stainless steel. Longer cooking durations resulted in additional increases in metal leaching, where Ni concentrations increased 34 fold and Cr increased approximately 35 fold from sauces cooked without stainless steel. Cooking with new stainless steel resulted in the largest increases. Metal leaching decreases with sequential cooking cycles and stabilized after the sixth cooking cycle, though significant metal contributions to foods were still observed. The tenth cooking cycle, resulted in an average of 88 μg of Ni and 86 μg of Cr leached per 126 g serving of tomato sauce. Stainless steel cookware can be an overlooked source of nickel and chromium, where the contribution is dependent on stainless steel grade, cooking time, and cookware usage. PMID:23984718

40 CFR 466.31 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2014 CFR

2014-07-01

... Chromium 16.34 6.32 6.63 2.56 Lead 5.84 2.26 5.06 1.96 Nickel 54.85 21.21 38.90 15.04 Zinc 51.73 20.01 21... ft2 of area processed or coated Chromium 3.35 1.30 1.37 0.53 Lead 1.20 0.47 1.04 0.40 Nickel 11.24 4...

40 CFR 466.31 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2011 CFR

2011-07-01

... Chromium 16.34 6.32 6.63 2.56 Lead 5.84 2.26 5.06 1.96 Nickel 54.85 21.21 38.90 15.04 Zinc 51.73 20.01 21... ft2 of area processed or coated Chromium 3.35 1.30 1.37 0.53 Lead 1.20 0.47 1.04 0.40 Nickel 11.24 4...

40 CFR 466.31 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2012 CFR

2012-07-01

... Chromium 16.34 6.32 6.63 2.56 Lead 5.84 2.26 5.06 1.96 Nickel 54.85 21.21 38.90 15.04 Zinc 51.73 20.01 21... ft2 of area processed or coated Chromium 3.35 1.30 1.37 0.53 Lead 1.20 0.47 1.04 0.40 Nickel 11.24 4...

40 CFR 466.31 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2013 CFR

2013-07-01

... Chromium 16.34 6.32 6.63 2.56 Lead 5.84 2.26 5.06 1.96 Nickel 54.85 21.21 38.90 15.04 Zinc 51.73 20.01 21... ft2 of area processed or coated Chromium 3.35 1.30 1.37 0.53 Lead 1.20 0.47 1.04 0.40 Nickel 11.24 4...

40 CFR 466.31 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2010 CFR

2010-07-01

... Chromium 16.34 6.32 6.63 2.56 Lead 5.84 2.26 5.06 1.96 Nickel 54.85 21.21 38.90 15.04 Zinc 51.73 20.01 21... ft2 of area processed or coated Chromium 3.35 1.30 1.37 0.53 Lead 1.20 0.47 1.04 0.40 Nickel 11.24 4...

Chromium exposure among children from an electronic waste recycling town of China.

PubMed

Xu, Xijin; Yekeen, Taofeek Akangbe; Liu, Junxiao; Zhuang, Bingrong; Li, Weiqiu; Huo, Xia

2015-02-01

Guiyu is one of the most heavily chromium-polluted areas in China due to the numerous informal electronic waste (e-waste) recycling activities. A 3-year (2004, 2006, and 2008) independent cross-sectional study on blood chromium (BCr) levels of 711 children from Guiyu and a control area was investigated. Questionnaire completed by parents/guardians was used to assess the risk factors of chromium (Cr) exposure, while physical examination, for the year 2008 only, was used to evaluate the effects of long-term exposure to Cr on child physical development. Children living in Guiyu had significantly higher BCr levels compared with those living in Chendian at the same period from 2004 to 2008 (P < 0.001). The predominant risk factors related to elevated child BCr levels included the use of house as a family workshop, parent involved in e-waste recycling, and child residence in Guiyu. Children's weight and chest circumferences in group with high exposure to Cr (upper quartile) were higher than in the low-exposure group (P < 0.01), although the difference was less significant for boys between the two groups (P < 0.05). The results suggest that elevated child BCr in Guiyu due to informal e-waste recycling activities might be threatening the health of children, with implications on physical growth and development.

Isolation and characterization of a chromium-resistant bacterium Serratia sp. Cr-10 from a chromate-contaminated site.

PubMed

Zhang, Kundi; Li, Fuli

2011-05-01

A novel bacterium, Cr-10, was isolated from a chromium-contaminated site and capable of removing toxic chromium species from solution by reducing hexavalent chromium to an insoluble precipitate. Sequence analysis of 16S rRNA gene of strain Cr-10 showed that it was most closely related to Serratia rubidaea JCM 1240(T) (97.68%). Physiological and chemotaxonomic data also supported that strain Cr-10 was identified as Serratia sp., a genus which was never specially reported chromate-resistant before. Serratia sp., Cr-10 was tolerant to a concentration of 1,500 mg Cr(VI) L(-1), which was the highest level reported until now. The optimum pH and temperature for reduction of Cr(VI) by Serratia sp. Cr-10 were found to be 7.0 and 37 °C, respectively. The Cr(VI) reduction was significantly influenced by additional carbon sources, and among them fructose and lactose offered maximum reduction, with a rate of 0.28 and 0.25 mg Cr(VI) L(-1) h(-1), respectively. The cell-free extracts and filtrate of the culture were able to reduce Cr(VI) while concentration of total chromium remained stable in the process, indicating that the enzyme-catalyzed mechanism was applied in Cr(VI) reduction by the isolate. Additionally, it was found that there was hardly any chromium on the cell surface of the strain, further supporting that reduction, rather than bioadsorption, plays a major role in the Cr(VI) removal.

Quantitative determination of chromium picolinate in animal feeds by solid phase extraction and liquid chromatography-tandem mass spectrometry.

PubMed

Han, Miaomiao; Tian, Ying; Li, Zhen; Chen, Yiqiang; Yang, Wenjun; Zhang, Liying

2017-12-01

Chromium picolinate is one of the important Cr 3+ resources and is widely used in animal production. A convenient, reliable and rapid liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for the quantitative determination of chromium picolinate in animal feeds. Feed samples were extracted with acetonitrile and subsequently cleaned up by solid phase extraction cartridges Supelclean™ LC-18. Chromium picolinate was efficiently separated with a Waters ACQUITY UPLC ® BEH C18 column, ionized with electrospray ion source in positive mode (ESI + ), and quantitatively determined by tandem mass spectrometry in multiple reaction monitoring mode. Standard calibration curve of chromium picolinate in the concentration range from 0.5 to 1000ng/mL was obtained with good linearity correlation coefficient (R 2 =0.9982). Average recoveries ranged from 95.37%∼105.54%, as detected by spiking 0.02∼640mg/kg of chromium picolinate in complete feed, concentrated feed and premix. Intra-day and inter-day coefficient of variation were 0.59%∼6.67% and 2.36%∼6.97%, respectively. The limits of quantitation were 0.02mg/kg, 0.025mg/kg, and 2mg/kg for complete feed, concentrated feed, and premix, respectively. Actual sample analysis indicated that the developed method can be an effective tool to monitoring CrPic content in animal feed. Copyright © 2017. Published by Elsevier B.V.

Chemical and microbial remediation of hexavalent chromium from contaminated soil and mining/metallurgical solid waste: a review.

PubMed

Dhal, B; Thatoi, H N; Das, N N; Pandey, B D

2013-04-15

Chromium is a highly toxic non-essential metal for microorganisms and plants, and its occurrence is rare in nature. Lower to higher chromium containing effluents and solid wastes released by activities such as mining, metal plating, wood preservation, ink manufacture, dyes, pigments, glass and ceramics, tanning and textile industries, and corrosion inhibitors in cooling water, induce pollution and may cause major health hazards. Besides, natural processes (weathering and biochemical) also contribute to the mobility of chromium which enters in to the soil affecting the plant growth and metabolic functions of the living species. Generally, chemical processes are used for Cr- remediation. However, with the inference derived from the diverse Cr-resistance mechanism displayed by microorganisms and the plants including biosorption, diminished accumulation, precipitation, reduction of Cr(VI) to Cr(III), and chromate efflux, bioremediation is emerging as a potential tool to address the problem of Cr(VI) pollution. This review focuses on the chemistry of chromium, its use, and toxicity and mobility in soil, while assessing its concentration in effluents/wastes which becomes the source of pollution. In order to conserve the environment and resources, the chemical/biological remediation processes for Cr(VI) and their efficiency have been summarised in some detail. The interaction of chromium with various microbial/bacterial strains isolated and their reduction capacity towards Cr(VI) are also discussed. Copyright © 2013 Elsevier B.V. All rights reserved.

Evaluation of quality-control data collected by the U.S. Geological Survey for routine water-quality activities at the Idaho National Laboratory, Idaho, 1996–2001

USGS Publications Warehouse

Rattray, Gordon W.

2012-01-01

The U.S. Geological Survey, in cooperation with the U.S. Department of Energy, collects surface water and groundwater samples at and near the Idaho National Laboratory as part of a routine, site-wide, water-quality monitoring program. Quality-control samples are collected as part of the program to ensure and document the quality of environmental data. From 1996 to 2001, quality-control samples consisting of 204 replicates and 27 blanks were collected at sampling sites. Paired measurements from replicates were used to calculate variability (as reproducibility and reliability) from sample collection and analysis of radiochemical, chemical, and organic constituents. Measurements from field and equipment blanks were used to estimate the potential contamination bias of constituents. The reproducibility of measurements of constituents was calculated from paired measurements as the normalized absolute difference (NAD) or the relative standard deviation (RSD). The NADs and RSDs, as well as paired measurements with censored or estimated concentrations for which NADs and RSDs were not calculated, were compared to specified criteria to determine if the paired measurements had acceptable reproducibility. If the percentage of paired measurements with acceptable reproducibility for a constituent was greater than or equal to 90 percent, then the reproducibility for that constituent was considered acceptable. The percentage of paired measurements with acceptable reproducibility was greater than or equal to 90 percent for all constituents except orthophosphate (89 percent), zinc (80 percent), hexavalent chromium (53 percent), and total organic carbon (TOC; 38 percent). The low reproducibility for orthophosphate and zinc was attributed to calculation of RSDs for replicates with low concentrations of these constituents. The low reproducibility for hexavalent chromium and TOC was attributed to the inability to preserve hexavalent chromium in water samples and high variability with the analytical method for TOC. The reliability of measurements of constituents was estimated from pooled RSDs that were calculated for discrete concentration ranges for each constituent. Pooled RSDs of 15 to 33 percent were calculated for low concentrations of gross-beta radioactivity, strontium-90, ammonia, nitrite, orthophosphate, nickel, selenium, zinc, tetrachloroethene, and toluene. Lower pooled RSDs of 0 to 12 percent were calculated for all other concentration ranges of these constituents, and for all other constituents, except for one concentration range for gross-beta radioactivity, chloride, and nitrate + nitrite; two concentration ranges for hexavalent chromium; and TOC. Pooled RSDs for the 50 to 60 picocuries per liter concentration range of gross-beta radioactivity (reported as cesium-137) and the 10 to 60 milligrams per liter (mg/L) concentration range of nitrate + nitrite (reported as nitrogen [N]) were 17 percent. Chloride had a pooled RSD of 14 percent for the 20 to less than 60 mg/L concentration range. High pooled RSDs of 40 and 51 percent were calculated for two concentration ranges for hexavalent chromium and of 60 percent for TOC. Measurements from (1) field blanks were used to estimate the potential bias associated with environmental samples from sample collection and analysis, (2) equipment blanks were used to estimate the potential bias from cross contamination of samples collected from wells where portable sampling equipment was used, and (3) a source-solution blank was used to verify that the deionized water source-solution was free of the constituents of interest. If more than one measurement was available, the bias was estimated using order statistics and the binomial probability distribution. The source-solution blank had a detectable concentration of hexavalent chromium of 2 micrograms per liter. If this bias was from a source other than the source solution, then about 84 percent of the 117 hexavalent chromium measurements from environmental samples could have a bias of 10 percent or more. Of the 14 field blanks that were collected, only chloride (0.2 milligrams per liter) and ammonia (0.03 milligrams per liter as nitrogen), in one blank each, had detectable concentrations. With an estimated confidencelevel of 95 percent, at least 80 percent of the 1,987 chloride concentrations measured from all environmental samples had a potential bias of less than 8 percent. The ammonia bias, which may have occurred at the analytical laboratory, could produce a potential bias of 5-100 percent in eight potentially affected ammonia measurements. Of the 11 equipment blanks that were collected, chloride was detected in 4 of these blanks, sodium in 3 blanks, and sulfate and hexavalent chromium were each detected in 1 blank. The concentration of hexavalent chromium in the equipment blank was the same concentration as in the source-solution blank collected on the same day, which indicates that the hexavalent chromium in the equipment blank is probably from a source other than the portable sampling equipment, such as the sample bottles or the source-solution water itself. The potential bias for chloride, sodium, and sulfate measurements was estimated for environmental samples that were collected using portable sampling equipment. For chloride, it was estimated with 93 percent confidence that at least 80 percent of the measurements had a bias of less than 18 percent. For sodium and sulfate, it was estimated with 91 percent confidence that at least 70 percent of the measurements had a bias of less than 12 and 5 percent, respectively.

Optical and spectroscopic studies on tannery wastes as a possible source of organic semiconductors.

PubMed

Nashy, El-Shahat H A; Al-Ashkar, Emad; Moez, A Abdel

2012-02-01

Tanning industry produces a large quantity of solid wastes which contain hide proteins in the form of protein shavings containing chromium salts. The chromium wastes are the main concern from an environmental stand point of view, because chrome wastes posses a significant disposal problem. The present work is devoted to investigate the possibility of utilizing these wastes as a source of organic semi-conductors as an alternative method instead of the conventional ones. The chemical characterization of these wastes was determined. In addition, the Horizontal Attenuated Total Reflection (HATR) FT-IR spectroscopic analysis and optical parameters were also carried out for chromated samples. The study showed that the chromated samples had suitable absorbance and transmittance in the wavelength range (500-850 nm). Presence of chromium salt in the collagen samples increases the absorbance which improves the optical properties of the studied samples and leads to decrease the optical energy gap. The obtained optical energy gap gives an impression that the environmentally hazardous chrome shavings wastes can be utilized as a possible source of natural organic semiconductors with direct and indirect energy gap. This work opens the door to use some hazardous wastes in the manufacture of electronic devices such as IR-detectors, solar cells and also as solar cell windows. Copyright © 2011 Elsevier B.V. All rights reserved.

Development of selective surfaces. Semiannual technical progress report, September 11, 1978-April 30, 1979. [Multilayer coatings

DOE Office of Scientific and Technical Information (OSTI.GOV)

Thornton, J.A.

1979-06-15

Magnetron sputtering technology, which permits coatings to be deposited over large areas with significantly increased deposition rates, is reviewed with particular emphasis on cylindrical magnetrons and their application to reactive sputtering. Work is reported in which cylindrical-post magnetron sputtering sources have been used to deposit both graded and multi-layered cermet-type coatings by sputtering chromium and type 304 stainless steel in Ar and O/sub 2/ and Ar and CO gas mixtures under various conditions of reactive gas injection. The substrates are aluminum-coated glass and aluminum foil. The coatings are of an interference type, typically about 100 nm thick, with a metal-rich,more » highly absorbing layer adjacent to the substrate and a dielectric material at the surface. In some cases a reactively sputtered aluminum oxide anti-reflective surface layer has also been used. No advantages have been found for using chromium as opposed to the more readily available stainless steel. The reactive sputtering with CO is attractive because under many conditions the sputtering rates are relatively large compared to oxygen. Hemispherical absorptance and emittance data are reported. Typical absorptances are about 0.90 with emittances of 0.10.« less

Iron, cadmium, and chromium in seagrass (Thalassia testudinum) from a coastal nature reserve in karstic Yucatán.

PubMed

Avelar, Mayra; Bonilla-Heredia, Blanca; Merino-Ibarra, Martín; Herrera-Silveira, Jorge A; Ramirez, Javier; Rosas, Humberto; Valdespino, Job; Carricart-Ganivet, Juan P; Martínez, Ana

2013-09-01

The management of protected areas in karstic regions is a challenge because flooded cave systems form there and provide underground hydrological conducts that may link different zones. As a consequence, affectations to the protected areas can possibly occur as a consequence of human activities in remote areas and may therefore pass undetected. Thus, the monitoring of possible contaminants in these regions is becoming imperative. In this work, we analyze the concentration of essential (iron) and non-essential metals (cadmium and chromium) in the seagrass Thalassia testudinum that grows in Yalahau Lagoon, located in a near-to-pristine protected area of the Yucatán Peninsula, close to the rapidly developing touristic belt of the Mexican Caribbean. Salinity and silicate patterns show that Yalahau is an evaporation lagoon, where groundwater discharge is important. High iron (> 400 μg/g), cadmium (>4 μg/g), and chromium (≈ 1 μg/g) concentrations were found in the area of highest groundwater input of the lagoon. High levels (5.1 μg/g) were also found near the town dump. In the rest of the sampling sites, metal concentrations remained near to background levels as estimated from other works. Temporal changes of concentrations in the seagrass tissues show also a local input and an input from the groundwater that could provoke an environmental problem in the Yalahau Lagoon in the near future.

Recovery Of Chromium Metal (VI) Using Supported Liquid Membrane (SLM) Method, A study of Influence of NaCl and pH in Receiving Phase on Transport

NASA Astrophysics Data System (ADS)

Cholid Djunaidi, Muhammad; Lusiana, Retno A.; Rahayu, Maya D.

2017-06-01

Chromium metal(VI) is a valuable metal but in contrary has high toxicity, so the separation and recovery from waste are very important. One method that can be used for the separation and recovery of chromium (VI) is a Supported Liquid Membrane (SLM). SLM system contains of three main components: a supporting membrane, organic solvents and carrier compounds. The supported Membrane used in this research is Polytetrafluoroethylene (PTFE), organic solvent is kerosene, and the carrier compound used is aliquat 336. The supported liquid membrane is placed between two phases, namely, feed phase as the source of analyte (Cr(VI)) and the receiving phase as the result of separation. Feed phase is the electroplating waste which contains of chromium metal with pH variation about 4, 6 and 9. Whereas the receiving phase are the solution of HCl, NaOH, HCl-NaCl and NaOH-NaCl with pH variation about 1, 3, 5 and 7. The efficiency separation is determined by measurement of chromium in the feed and the receiving phase using AAS (Atomic Absorption Spectrophotometry). The experiment results show that transport of Chrom (VI) by Supported Liquid membrane (SLM) is influenced by pH solution in feed phase and receiving phase as well as NaCl in receiving phase. The highest chromium metal is transported from feed phase about 97,78%, whereas in receiving phase shows about 58,09%. The highest chromium metal transport happens on pH 6 in feed phase, pH 7 in receiving phase with the mixture of NaOH and NaCl using carrier compound aliquat 336.

[Slow-release recombinant human bone morphogenetic protein-2 suppresses chromium wear particle-induced osteolysis in rats].

PubMed

Li, Gan; Li, Qi; Lin, Li-Jun; Duan, Xin; Zhang, Xi-Qi

2012-03-01

To observe the effect of a slow-release recombinant human bone morphogenetic protein-2 (rhBMP-2) formulation on the expressions of receptor activator of nuclear factor-κB ligand (RANKL) and osteoprotegerin (OPG) in a murine air pouch model of bone implantation. A cranial bone allograft was implanted in the air pouch induced on the back of the recipients. The rat models were then randomized into 5 groups, including a blank control group, chromium particle group, and 3 rhBMP-2 groups receiving 50, 100 or 200 µg/L slow-release rhBMP-2 in addition to chromium particles. Three weeks later, the expressions of RANKL and OPG in the air pouch was detected using Western blotting and RT-PCR, and the positively stained area for osteoclasts in the bone graft was determined with TRAP staining for drug effect assessment. RANKL and OPG expressions were found in the air pouches in all the 5 groups. RANKL and OPG protein and mRNA expressions, RANKL/OPG ratio and osteoclast staining area in the bone graft were the highest in chromium particle group (P<0.05), but were significantly decreased by treatment with the slow-release rhBMP-2 formulation (P<0.05); the measurements showed no significant differences between the blank control group and 200 µg/L rhBMP-2 group (P>0.05). Chromium particles can cause osteolysis by increasing the RANKL/OPG ratio in rats, and intervention with slow-release rhBMP-2 can significantly promote bone formation and suppress bone resorption by decreasing RANKL/OPG ratio.

40 CFR 63.345 - Provisions for new and reconstructed sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

... completion dates of the construction or reconstruction; (vi) The anticipated date of (initial) startup of the affected source; (vii) The type of process operation to be performed (hard or decorative chromium... startup had not occurred before January 25, 1995, the notification shall be submitted as soon as...

40 CFR 63.345 - Provisions for new and reconstructed sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

... completion dates of the construction or reconstruction; (vi) The anticipated date of (initial) startup of the affected source; (vii) The type of process operation to be performed (hard or decorative chromium... startup had not occurred before January 25, 1995, the notification shall be submitted as soon as...

40 CFR 63.345 - Provisions for new and reconstructed sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

... completion dates of the construction or reconstruction; (vi) The anticipated date of (initial) startup of the affected source; (vii) The type of process operation to be performed (hard or decorative chromium... startup had not occurred before January 25, 1995, the notification shall be submitted as soon as...

40 CFR 467.36 - Pretreatment standards for new sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

.... 467.36 Section 467.36 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Extrusion Subcategory § 467.36 Pretreatment... day Maximum for monthly average mg/off-kg (lb/million off-lbs) of extruded Chromium 0.13 0.05 Cyanide...

40 CFR 421.274 - Standards of performance for new sources.

Code of Federal Regulations, 2012 CFR

2012-07-01

...) EFFLUENT GUIDELINES AND STANDARDS NONFERROUS METALS MANUFACTURING POINT SOURCE CATEGORY Primary Rare Earth... Scrubber. NSPS for the Primary Rare Earth Metals Subcategory Pollutant or pollutant property Maximum for... wet rare earth chlorides Hexachlorobenzene 0.042 0.042 Chromium (total) 1.544 0.626 Lead 1.168 0.542...

40 CFR 421.274 - Standards of performance for new sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

...) EFFLUENT GUIDELINES AND STANDARDS NONFERROUS METALS MANUFACTURING POINT SOURCE CATEGORY Primary Rare Earth... Scrubber. NSPS for the Primary Rare Earth Metals Subcategory Pollutant or pollutant property Maximum for... wet rare earth chlorides Hexachlorobenzene 0.042 0.042 Chromium (total) 1.544 0.626 Lead 1.168 0.542...

40 CFR 421.274 - Standards of performance for new sources.

Code of Federal Regulations, 2013 CFR

2013-07-01

...) EFFLUENT GUIDELINES AND STANDARDS NONFERROUS METALS MANUFACTURING POINT SOURCE CATEGORY Primary Rare Earth... Scrubber. NSPS for the Primary Rare Earth Metals Subcategory Pollutant or pollutant property Maximum for... wet rare earth chlorides Hexachlorobenzene 0.042 0.042 Chromium (total) 1.544 0.626 Lead 1.168 0.542...

40 CFR 421.274 - Standards of performance for new sources.

Code of Federal Regulations, 2010 CFR

2010-07-01

...) EFFLUENT GUIDELINES AND STANDARDS NONFERROUS METALS MANUFACTURING POINT SOURCE CATEGORY Primary Rare Earth... Scrubber. NSPS for the Primary Rare Earth Metals Subcategory Pollutant or pollutant property Maximum for... wet rare earth chlorides Hexachlorobenzene 0.042 0.042 Chromium (total) 1.544 0.626 Lead 1.168 0.542...

40 CFR 421.274 - Standards of performance for new sources.

Code of Federal Regulations, 2014 CFR

2014-07-01

...) EFFLUENT GUIDELINES AND STANDARDS NONFERROUS METALS MANUFACTURING POINT SOURCE CATEGORY Primary Rare Earth... Scrubber. NSPS for the Primary Rare Earth Metals Subcategory Pollutant or pollutant property Maximum for... wet rare earth chlorides Hexachlorobenzene 0.042 0.042 Chromium (total) 1.544 0.626 Lead 1.168 0.542...

The effect of chromium picolinate and biotin supplementation on glycemic control in poorly controlled patients with type 2 diabetes mellitus: a placebo-controlled, double-blinded, randomized trial.

PubMed

Singer, Gregory M; Geohas, Jeff

2006-12-01

Preclinical studies have shown that the combination of chromium picolinate and biotin significantly enhances glucose uptake in skeletal muscle cells and enhances glucose disposal. The present pilot study was conducted to determine if supplementation with chromium picolinate and biotin can improve glycemic control in patients with type 2 diabetes mellitus with suboptimal glycemic control despite use of oral antihyperglycemic agents. Forty-three subjects with impaired glycemic control (2-h glucose >200 mg/dL; glycated hemoglobin >or=7%), despite treatments with oral antihyperglycemic agents, were randomized to receive 600 microg of chromium as chromium picolinate and biotin (2 mg/day) (Diachrome(, Nutrition 21, Inc., Purchase, NY) in addition to their prestudy oral antihyperglycemic agent therapy. Measurements of glycemic control and blood lipids were taken at baseline and after 4 weeks. After 4 weeks, there was a significantly greater reduction in the total area under the curve for glucose during the 2-h oral glucose tolerance test for the treatment group (mean change -9.7%) compared with the placebo group (mean change +5.1%, P < 0.03). Significantly greater reductions were also seen in fructosamine (P < 0.03), triglycerides (P < 0.02), and triglycerides/ high-density lipoprotein cholesterol ratio (P < 0.05) in the treatment group. No significant adverse events were attributed to chromium picolinate and biotin supplementation. This pilot study demonstrates that supplementation with a combination of chromium picolinate and biotin in poorly controlled patients with diabetes receiving antidiabetic therapy improved glucose management and several lipid measurements. Chromium picolinate/ biotin supplementation may represent an effective adjunctive nutritional therapy to people with poorly controlled diabetes with the potential for improving lipid metabolism.

Selective and sensitive detection of chromium(VI) in waters using electrospray ionization mass spectrometry.

PubMed

Weldy, Effie; Wolff, Chloe; Miao, Zhixin; Chen, Hao

2013-09-01

From 2000 through 2011, there were 14 criminal cases of violations of the Clean Water Act involving the discharge of chromium, a toxic heavy metal, into drinking and surface water sources. As chromium(VI), a potential carcinogen present in the environment, represents a significant safety concern, it is currently the subject of an EPA health risk assessment. Therefore, sensitive and selective detection of this species is highly desired. This study reports the analysis of chromium(VI) in water samples by electrospray ionization mass spectrometry (ESI-MS) following its reduction and complexation with ammonium pyrrolidinedithiocarbamate (APDC). The reduction and subsequent complexation produce a characteristic [Cr(III)O]-PDC complex which can be detected as a protonated ion of m/z 507 in the positive ion mode. The detection is selective to chromium(VI) under acidic pH, even in the presence of chromium(III) and other metal ions, providing high specificity. Different water samples were examined, including deionized, tap, and river waters, and sensitive detection was achieved. In the case of deionized water, quantification over the concentration range of 3.7 to 148ppb gave an excellent correlation coefficient of 0.9904 using the enhanced MS mode scan. Using the single-reaction monitoring (SRM) mode (monitoring the characteristic fragmentation of m/z 507 to m/z 360), the limit of detection (LOD) was found to be 0.25ppb. The LOD of chromium(VI) for both tap and river water samples was determined to be 2.0ppb. A preconcentration strategy using simple vacuum evaporation of the aqueous sample was shown to further improve the ESI signal by 15 fold. This method, with high sensitivity and selectivity, should provide a timely solution for the real-world analysis of toxic chromium(VI). Copyright © 2012 Forensic Science Society. Published by Elsevier Ireland Ltd. All rights reserved.

Fabrication of Size-Tunable Metallic Nanoparticles Using Plasmid DNA as a Biomolecular Reactor

PubMed Central

Samson, Jacopo; Piscopo, Irene; Yampolski, Alex; Nahirney, Patrick; Parpas, Andrea; Aggarwal, Amit; Saleh, Raihan; Drain, Charles Michael

2011-01-01

Plasmid DNA can be used as a template to yield gold, palladium, silver, and chromium nanoparticles of different sizes based on variations in incubation time at 70 °C with gold phosphine complexes, with the acetates of silver or palladium, or chromium acetylacetonate. The employment of mild synthetic conditions, minimal procedural steps, and aqueous solvents makes this method environmentally greener and ensures general feasibility. The use of plasmids exploits the capabilities of the biotechnology industry as a source of nanoreactor materials. PMID:28348280

Biodegradation of orthodontic appliances and their effects on the blood level of nickel and chromium. Master's thesis

DOE Office of Scientific and Technical Information (OSTI.GOV)

Barrett, R.D.

1990-05-01

Austenitic stainless steels containing approximately 18 percent chromium and 8 percent nickel for orthodontic bands, brackets and wires is universally used in orthodontic practices. With the introduction of nickel-titanium alloys as orthodontic archwires in the 1970's an additional source of patient exposure to metal corrosion products has been introduced. Since the oral environment is particularly ideal for the biodegradation of metals due to its ionic, thermal, microbiologic and enzymatic properties some level of patient exposure to the corrosion products of these alloys is assured.

The x ray microprobe determination of chromium oxidation state in olivine from lunar basalt and kimberlitic diamonds

NASA Technical Reports Server (NTRS)

Sutton, S. R.; Bajt, S.; Rivers, M. L.; Smith, J. V.

1993-01-01

The synchrotron x-ray microprobe is being used to obtain oxidation state information on planetary materials with high spatial resolution. Initial results on chromium in olivine from various sources including laboratory experiments, lunar basalt, and kimberlitic diamonds are reported. The lunar olivine was dominated by Cr(2+) whereas the diamond inclusions had Cr(2+/Cr(3+) ratios up to about 0.3. The simpliest interpretation is that the terrestrial olivine crystallized in a more oxidizing environment than the lunar olivine.

Removal of aqueous chromium and environmental CO2 by using photocatalytic TiO2 doped with tungsten.

PubMed

Trejo-Valdez, M; Hernández-Guzmán, S R; Manriquez-Ramírez, M E; Sobral, H; Martínez-Gutiérrez, H; Torres-Torres, C

2018-05-15

Removal of hexavalent chromium was accomplished by using photocatalyst materials of TiO 2 doped with tungsten oxide, environmental air as oxygen supply and white light as irradiation source. Dichromate anions in concentration ranges of 50 to 1000 μg/L were removed by means of aqueous dispersions of TiO 2 doped with tungsten. The aqueous chromium analyses were performed by Differential Pulse Voltammetry technique. Additionally, mineralization of CO 2 gas was promoted by the photocatalysis process, as was clearly shown by Raman spectroscopy and X-ray Photoelectron Spectroscopy (XPS) analyses obtained from the TiO 2 samples recovered after photocatalytic experiments. Results of sample analyses by Scanning Electron Microscopy (SEM) and High Resolution Transmission Electron Microscopy (HRTEM) are presented and discussed. Copyright © 2018 Elsevier B.V. All rights reserved.

40 CFR 437.24 - New source performance standards (NSPS).

Code of Federal Regulations, 2010 CFR

2010-07-01

..., TSS, arsenic, cadmium, chromium, cobalt, copper, lead, mercury, tin, zinc, butylbenzyl phthalate, carbazole, n-decane, bis(2-ethylhexyl) phthalate, fluoranthene, and n-octadecane are the same as the...

40 CFR 437.24 - New source performance standards (NSPS).

Code of Federal Regulations, 2011 CFR

2011-07-01

..., TSS, arsenic, cadmium, chromium, cobalt, copper, lead, mercury, tin, zinc, butylbenzyl phthalate, carbazole, n-decane, bis(2-ethylhexyl) phthalate, fluoranthene, and n-octadecane are the same as the...

Genesis of hexavalent chromium from natural sources in soil and groundwater.

PubMed

Oze, Christopher; Bird, Dennis K; Fendorf, Scott

2007-04-17

Naturally occurring Cr(VI) has recently been reported in ground and surface waters. Rock strata rich in Cr(III)-bearing minerals, in particular chromite, are universally found in these areas that occur near convergent plate margins. Here we report experiments demonstrating accelerated dissolution of chromite and subsequent oxidation of Cr(III) to aqueous Cr(VI) in the presence of birnessite, a common manganese mineral, explaining the generation of Cr(VI) by a Cr(III)-bearing mineral considered geochemically inert. Our results demonstrate that Cr(III) within ultramafic- and serpentinite-derived soils/sediments can be oxidized and dissolved through natural processes, leading to hazardous levels of aqueous Cr(VI) in surface and groundwater.

Genesis of hexavalent chromium from natural sources in soil and groundwater

PubMed Central

Oze, Christopher; Bird, Dennis K.; Fendorf, Scott

2007-01-01

Naturally occurring Cr(VI) has recently been reported in ground and surface waters. Rock strata rich in Cr(III)-bearing minerals, in particular chromite, are universally found in these areas that occur near convergent plate margins. Here we report experiments demonstrating accelerated dissolution of chromite and subsequent oxidation of Cr(III) to aqueous Cr(VI) in the presence of birnessite, a common manganese mineral, explaining the generation of Cr(VI) by a Cr(III)-bearing mineral considered geochemically inert. Our results demonstrate that Cr(III) within ultramafic- and serpentinite-derived soils/sediments can be oxidized and dissolved through natural processes, leading to hazardous levels of aqueous Cr(VI) in surface and groundwater. PMID:17420454

Review of the general geology and solid-phase geochemical studies in the vicinity of the Central Oklahoma aquifer

USGS Publications Warehouse

Mosier, Elwin L.; Bullock, John H.

1988-01-01

The Central Oklahoma aquifer is the principal source of ground water for municipal, industrial, and rural use in central Oklahoma. Ground water in the aquifer is contained in consolidated sedimentary rocks consisting of the Admire, Council Grove, and Chase Groups, Wellington Formation, and Garber Sandstone and in the unconsolidated Quaternary alluvium and terrace deposits that occur along the major stream systems in the study area. The Garber Sandstone and the Wellington Formation comprise the main flow system and, as such, the aquifer is often referred to as the 'Garber-Wellington aquifer.' The consolidated sedimentary rocks consist of interbedded lenticular sandstone, shale, and siltstone beds deposited in similar deltaic environments in early Permian time. Arsenic, chromium, and selenium are found in the ground water of the Central Oklahoma aquifer in concentrations that, in places, exceed the primary drinking-water standards of the Environmental Protection Agency. Gross-alpha concentrations also exceed the primary standards in some wells, and uranium concentrations are uncommonly high in places. As a prerequisite to a surface and subsurface solid-phase geochemical study, this report summarizes the general geology of the Central Oklahoma study area. Summaries of results from certain previously reported solid-phase geochemical studies that relate to the vicinity of the Central Oklahoma aquifer are also given; including a summary of the analytical results and distribution plots for arsenic, selenium, chromium, thorium, uranium, copper, and barium from the U.S. Department of Energy's National Uranium Resource Evaluation (NURE) Program.

Star tracking reticles

NASA Technical Reports Server (NTRS)

Smith, W. O.; Toft, A. R. (Inventor)

1973-01-01

A method for the production of reticles, particularly those for use in outer space, where the product is a quartz base coated with highly adherent layers of chromium, chromium-silver, and silver vacuum deposited through a mask, and then coated with an electrodeposit of copper from a copper sulfate solution followed by an electrodeposit of black chromium is described. The masks are produced by coating a beryllium-copper alloy substrate with a positive working photoresist, developing the photoresist, according to a pattern to leave a positive mask, plating uncoated areas with gold, removing the photoresist, coating the substrate with a negative working photoresist, developing the negative working photoresist to expose the base metal of the pattern, and chemically etching the unplated side of the pattern to produce the mask.

40 CFR 421.245 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... existing sources. The mass of wastewater pollutants in secondary nickel process wastewater introduced into.../kg (pounds per million pounds) of slag input to reclaim process Chromium (total) 5.653 2.313 Copper 24.410 12.850 Nickel 24.670 16.320 (b) Acid reclaim leaching filtrate. PSES for the Secondary Nickel...

The Structure and Properties of Plasma Sprayed Iron Oxide Doped Manganese Cobalt Oxide Spinel Coatings for SOFC Metallic Interconnectors

NASA Astrophysics Data System (ADS)

Puranen, Jouni; Lagerbom, Juha; Hyvärinen, Leo; Kylmälahti, Mikko; Himanen, Olli; Pihlatie, Mikko; Kiviaho, Jari; Vuoristo, Petri

2011-01-01

Manganese cobalt oxide spinel doped with Fe2O3 was studied as a protective coating on ferritic stainless steel interconnects. Chromium alloying causes problems at high operation temperatures in such oxidizing conditions where chromium compounds evaporate and poison the cathode active area, causing the degradation of the solid oxide fuel cell. In order to prevent chromium evaporation, these interconnectors need a protective coating to block the chromium evaporation and to maintain an adequate electrical conductivity. Thermal spraying is regarded as a promising way to produce dense and protective layers. In the present work, the ceramic Mn-Co-Fe oxide spinel coatings were produced by using the atmospheric plasma spray process. Coatings with low thickness and low amount of porosity were produced by optimizing deposition conditions. The original spinel structure decomposed because of the fast transformation of solid-liquid-solid states but was partially restored by using post-annealing treatment.

Bioremediation of chromium by the yeast Pichia guilliermondii: toxicity and accumulation of Cr (III) and Cr (VI) and the influence of riboflavin on Cr tolerance.

PubMed

Ksheminska, Helena; Jaglarz, Anita; Fedorovych, Daria; Babyak, Lyubov; Yanovych, Dmytro; Kaszycki, Pawel; Koloczek, Henryk

2003-01-01

A comparative study has been made on the sensitivity of the yeast Pichia guilliermondii to Cr (III) and Cr (VI) as well as on the Cr uptake potential at growth-inhibitory concentrations of chromium. The strains used in the study were either isolated from natural sources or obtained from a laboratory strain collection. The results show that most of the natural strains were more tolerant to chromium and were able to grow in the presence of 5 mM Cr (III) or 0.5 mM Cr (VI), that is at concentrations which substantially inhibited the growth of laboratory strains. The cellular Cr content after treatment was similar for both strain types and ranged from 1.2-4.0 mg/g d.w. and 0.4-0.9 mg/g d.w., for Cr (III) and Cr (VI) forms, respectively, however, in one case of a natural strain it reached the value of 10 mg Cr (III)/g dry mass. Natural-source strains were grouped into four groups based on the yeasts' differential response to Cr (III) and Cr (VI). Hexavalent Cr-resistant mutants of a P. giuilliermondii laboratory strain, which revealed markedly changed capabilities of chromium accumulation, were obtained by means of UV-induced mutagenesis. Cr (VI) treatment triggered oversynthesis of riboflavin and the addition of exogenous riboflavin increased P. guilliermondii resistance to both Cr (III) and Cr (VI). Electrophoretic protein profiles revealed the induction and/or suppression of several proteins in response to toxic Cr (VI) levels.

Oral ingestion of hexavalent chromium through drinking water and cancer mortality in an industrial area of Greece - An ecological study

PubMed Central

2011-01-01

Background Hexavalent chromium is a known carcinogen when inhaled, but its carcinogenic potential when orally ingested remains controversial. Water contaminated with hexavalent chromium is a worldwide problem, making this a question of significant public health importance. Methods We conducted an ecological mortality study within the Oinofita region of Greece, where water has been contaminated with hexavalent chromium. We calculated gender, age, and period standardized mortality ratios (SMRs) for all deaths, cancer deaths, and specific cancer types of Oinofita residents over an 11-year period (1999 - 2009), using the greater prefecture of Voiotia as the standard population. Results A total of 474 deaths were observed. The SMR for all cause mortality was 98 (95% CI 89-107) and for all cancer mortality 114 (95% CI 94-136). The SMR for primary liver cancer was 1104 (95% CI 405-2403, p-value < 0.001). Furthermore, statistically significantly higher SMRs were identified for lung cancer (SMR = 145, 95% CI 100-203, p-value = 0.047) and cancer of the kidney and other genitourinary organs among women (SMR = 368, 95% CI 119-858, p-value = 0.025). Elevated SMRs for several other cancers were also noted (lip, oral cavity and pharynx 344, stomach 121, female breast 134, prostate 128, and leukaemias 168), but these did not reach statistical significance. Conclusions Elevated cancer mortality in the Oinofita area of Greece supports the hypothesis of hexavalent chromium carcinogenicity via the oral ingestion pathway of exposure. Further studies are needed to determine whether this association is causal, and to establish preventive guidelines and public health recommendations. PMID:21609468

Organic and metal contamination in marine surface sediments of Guánica Bay, Puerto Rico.

PubMed

Whitall, David; Mason, Andrew; Pait, Anthony; Brune, Lia; Fulton, Michael; Wirth, Ed; Vandiver, Lisa

2014-03-15

Land based sources of pollution have the potential to adversely impact valuable coral reef ecosystems. In Guánica Bay (Puerto Rico) sediment samples collected and analyzed in 2009 demonstrate unusually high concentrations of total chlordane, total PCBs, nickel and chromium. A variety of other contaminants (total DDT, total PAHs, As, Cu, Hg, and Zn) were also at levels which may indicate sediment toxicity. With the exception of chromium, all of these contaminants were detected in coral tissues (Porites astreoides), although it is unclear at what level these contaminants affect coral health. PCBs and chlordane are environmentally persistent and likely represent legacy pollution from historical uses in close geographic proximity to the Bay. We hypothesize that the high nickel and chromium levels are due to a combination of naturally high Ni and Cr in rock and soils in the watershed, and enhanced (human driven) erosional rates. Published by Elsevier Ltd.

A fundamental study of chromium deposition on solid oxide fuel cell cathode materials

NASA Astrophysics Data System (ADS)

Tucker, Michael C.; Kurokawa, Hideto; Jacobson, Craig P.; De Jonghe, Lutgard C.; Visco, Steven J.

Chromium contamination of metal oxides and SOFC cathode catalysts is studied in the range 700-1000 °C. Samples are exposed to a moist air atmosphere saturated with volatile Cr species in the presence and absence of direct contact between the sample and ferritic stainless steel powder. Chromium contamination of the samples is observed to occur via two separate pathways: surface diffusion from the stainless steel surface and vapor deposition from the atmosphere. Surface diffusion dominates in all cases. Surface diffusion is found to be a significant source of Cr contamination for LSM and LSCF at 700, 800, and 1000 °C. Vapor deposition of Cr onto LSCF was observed at each of these temperatures, but was not observed for LSM at 700 or 800 °C. Comparison of the behavior for LSM, LSCF, and single metal oxides suggests that Mn and Co, respectively, are responsible for the Cr contamination of these catalysts.

Bioaccumulation of Copper (Cu) and Chromium (Cr) on export comodity vanamei shrimp from Karawang, West Java

NASA Astrophysics Data System (ADS)

Rahman, A.; Takarina, N. D.; Siswantining, T.; Pin, T. G.; Soedjiarti, T.

2018-05-01

Karawang is one of regencies in West Java which has great potential for vannamei culture. The farm here was modern farm and using Citarum River as water source. Human activities like household and industry around the river cause its quality decrease and give negative impact to shrimp farm. This research was aimed to investigate the bioaccumulation of copper (Cu) and chromium (Cr) on vannamei shrimp from Karawang, West Java. Amount of shrimp’s meat and carapace were used for heavy metal measurement using Atomic Absorption Specthrophotometry. Result showed that contents of copper both in meat and carapace were higher than content of chromium. Moreover, the content of both metals was higher on carapace compared to meat. Since the content of meat were below threshold, so it is safe for consumption. There is no significant difference content of both metals in carapace.

Mussels and clams from the italian fish market. is there a human exposition risk to metals and arsenic?

PubMed

Chiesa, L M; Ceriani, F; Caligara, M; Di Candia, D; Malandra, R; Panseri, S; Arioli, F

2018-03-01

Seafood is associated with many beneficial effects on human health. However, the overall level of contaminants in biota has increased over the last two centuries and seafood is one of the source of oral exposition to contaminants. Therefore, this work aimed to evaluate cadmium, lead, mercury, arsenic, chromium and nickel presence in mussels and clams, from the Italian market, and the associated risk. The samples were from five different FAO areas. Analyses were carried out using inductively-coupled plasms-mass spectrometry. The sample concentrations were below the maximum levels stated by Commission Regulation (EC) 1881/2006, except one mussel sample, which was non-compliant for cadmium (2.13 ± 0.20 mg kg -1 ). For arsenic, nickel and chromium, maximum levels are not stated by the European Union. In this study, arsenic ranged from 1.29 to 13.35 mg kg -1 and nickel ranged from 1, and BMDL 10 for lung bladder and skin cancer in all mussel samples was overcome, in the 100% and 25% of mussel and clam samples, respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

40 CFR 467.55 - Pretreatment standards for existing sources.

Code of Federal Regulations, 2011 CFR

2011-07-01

... any 1 day Maximum for monthly average mg/off-kg (lb/million off-lbs) of aluminum drawn with neat oils Chromium 0.022 0.009 Cyanide 0.015 0.006 Zinc 0.073 0.031 TTO 0.035 Oil and grease (alternate monitoring...) EFFLUENT GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Neat Oils Subcategory...

40 CFR 461.73 - New source performance standards. (NSPS).

Code of Federal Regulations, 2011 CFR

2011-07-01

...) EFFLUENT GUIDELINES AND STANDARDS BATTERY MANUFACTURING POINT SOURCE CATEGORY Zinc Subcategory § 461.73 New... subject to this subpart shall not exceed the standards set forth below: (1) Subpart G—Zinc Oxide Formed... units—mg/kg of zinc English units—pounds per 1,000,000 pounds of zinc Chromium 4.55 1.97 Mercury 2.82 1...

The reactivity of Fe(II) associated with goethite formed during short redox cycles toward Cr(VI) reduction under oxic conditions

DOE Office of Scientific and Technical Information (OSTI.GOV)

Tomaszewski, Elizabeth J.; Lee, Seungyeol; Rudolph, Jared

Chromium (Cr) is a toxic metal that causes a myriad of health problems and enters the environment as a result of anthropogenic activities and/or natural processes. The toxicity and solubility of chromium is linked to its oxidation state; Cr(III) is poorly soluble and relatively nontoxic, while Cr(VI) is soluble and a known carcinogen. Solid Fe(II) in iron-bearing minerals, such as pyrite, magnetite, and green rusts, reduce the oxidation state of chromium, reducing its toxicity and mobility. However, these minerals are not the only potential sources of solid-associated Fe(II) available for Cr(VI) reduction. For example, ferric (Fe(III)) (hydr)oxides, such as goethitemore » or hematite, can have Fe(II) in the solid without phase transformation; however, the reactivity of Fe(II) within Fe(III) (hydr)oxides with contaminants, has not been previously investigated. Here, we cyclically react goethite with dissolved Fe(II) followed by dissolved O2, leading to the formation of reactive Fe(II) associated with goethite. In separate reactors, the reactivity of this Fe(II) is probed under oxic conditions, by exposure to chromate (CrO42 -) after either one, two, three or four redox cycles. Cr is not present during redox cycling; rather, it is introduced to a subset of the solid after each oxidation half-cycle. Analysis of X-ray absorption near edge structure (XANES) spectra reveals that the extent of Cr(VI) reduction to Cr(III) depends not only on solid Fe(II) content but also surface area and mean size of ordered crystalline domains, determined by BET surface area analysis and X-ray diffraction (XRD), respectively. Shell-by-shell fitting of the extended X-ray absorption fine structure (EXAFS) spectra demonstrates chromium forms both single and double corner sharing complexes on the surface of goethite, in addition to sorbed Cr(III) species. Finally, transmission electron microscope (TEM) imaging and X-ray energy-dispersive spectroscopy (EDS) illustrate that Cr preferentially localizes on the (100) face of goethite, independent of the number of redox cycles goethite undergoes. This work demonstrates that under oxic conditions, solid Fe(II) associated with goethite resulting from rapid redox cycling is reactive and available for electron transfer to Cr(VI), suggesting Fe(III) (hydr)oxides may act as reservoirs of reactive electron density, even in oxygen saturated environments.« less

40 CFR 437.15 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2011 CFR

2011-07-01

..., cadmium, chromium, cobalt, copper, lead, mercury, nickel, silver, tin, titanium, vanadium, and zinc are the same as the corresponding limitation specified in § 437.11(a). (b) In-plant standards for cyanide...

40 CFR 471.95 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... I—PSNS. There shall be no discharge of process wastewater pollutants. (p) Molten salt rinse. Subpart... (pounds per million off-pounds) of zirconium-hafnium rinsed following molten salt treatment Chromium 0.333...

40 CFR 471.95 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... I—PSNS. There shall be no discharge of process wastewater pollutants. (p) Molten salt rinse. Subpart... (pounds per million off-pounds) of zirconium-hafnium rinsed following molten salt treatment Chromium 0.333...

40 CFR 471.95 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... I—PSNS. There shall be no discharge of process wastewater pollutants. (p) Molten salt rinse. Subpart... (pounds per million off-pounds) of zirconium-hafnium rinsed following molten salt treatment Chromium 0.333...

Environmental exposure to arsenic and chromium in children is associated with kidney injury molecule-1

DOE Office of Scientific and Technical Information (OSTI.GOV)

Cárdenas-González, M.

Environmental hazards from natural or anthropological sources are widespread, especially in the north-central region of Mexico. Children represent a susceptible population due to their unique routes of exposure and special vulnerabilities. In this study we evaluated the association of exposure to environmental kidney toxicants with kidney injury biomarkers in children living in San Luis Potosi (SLP), Mexico. A cross-sectional study was conducted with 83 children (5–12 years of age) residents of Villa de Reyes, SLP. Exposure to arsenic, cadmium, chromium, fluoride and lead was assessed in urine, blood and drinking water samples. Almost all tap and well water samples hadmore » levels of arsenic (81.5%) and fluoride (100%) above the permissible levels recommended by the World Health Organization. Mean urine arsenic (45.6 ppb) and chromium (61.7 ppb) were higher than the biological exposure index, a reference value in occupational settings. Using multivariate adjusted models, we found a dose-dependent association between kidney injury molecule-1 (KIM-1) across chromium exposure tertiles [(T1: reference, T2: 467 pg/mL; T3: 615 pg/mL) (p-trend=0.001)]. Chromium upper tertile was also associated with higher urinary miR-200c (500 copies/μl) and miR-423 (189 copies/μL). Arsenic upper tertile was also associated with higher urinary KIM-1 (372 pg/mL). Other kidney injury/functional biomarkers such as serum creatinine, glomerular filtration rate, albuminuria, neutrophil gelatinase-associated lipocalin and miR-21 did not show any association with arsenic, chromium or any of the other toxicants evaluated. We conclude that KIM-1 might serve as a sensitive biomarker to screen children for kidney damage induced by environmental toxic agents. - Highlights: • Children living in Mexico had exceedingly high arsenic and chromium exposure. • Arsenic and chromium exposure was significantly associated with urinary KIM-1. • KIM-1 might serve as a sensitive biomarker to evaluate kidney injury in children.« less

[Dihydrotestosterone improves the osseointegration of cobalt-chromium implants].

PubMed

Maus, U M; Lühmann, M; Ohnsorge, J A K; Andereya, S; Schmidt, H; Zombory, G; Siebert, C; Niedhart, C

2013-02-01

The osseointegration of actually rarely implanted cobalt-chromium implants can be critical in an elderly population. The aim of our study was to evaluate the effect of preoperative testosterone treatment on the osseointegration of cobalt-chromium implants. Press-fit implantation of 1.6 mm-diameter cobalt-chromium-molybdenum (CoCrMo) implants was performed in rats without pre-treatment in one group (n = 10) and after pre-treatment with 1 mg dihydrotestosterone (DHT) 2 days before surgery in the other group (n = 10). After 14 days, the specimens were examined by a pull-out test, histology and histomorphometry. The biomechanical testing delivered inconsistent data leading to no significant difference (6.45 ± 6.94 N vs. 4.66 ± 3.77 N). Histology showed closed contact between surrounding tissue and the implants in both groups. The bone/implant contact area was significantly enhanced after treatment with DHT (42.23 % ± 9.25 vs. 57.57 % ± 16.71, p < 0.05), while the ratio of osteoid was reduced (38.68 % ± 16.7 vs. 27.38 % ± 13.02, not significant). Pre-treatment with DHT enhances osseointegration of cobalt-chromium implants through enhanced mineralisation of peri-implant tissue. The treatment might additionally shorten postoperative rehabilitation due to its positive effects on musculature. Georg Thieme Verlag KG Stuttgart · New York.

Environmental exposure to arsenic and chromium in children is associated with kidney injury molecule-1.

PubMed

Cárdenas-González, M; Osorio-Yáñez, C; Gaspar-Ramírez, O; Pavković, M; Ochoa-Martínez, A; López-Ventura, D; Medeiros, M; Barbier, O C; Pérez-Maldonado, I N; Sabbisetti, V S; Bonventre, J V; Vaidya, V S

2016-10-01

Environmental hazards from natural or anthropological sources are widespread, especially in the north-central region of Mexico. Children represent a susceptible population due to their unique routes of exposure and special vulnerabilities. In this study we evaluated the association of exposure to environmental kidney toxicants with kidney injury biomarkers in children living in San Luis Potosi (SLP), Mexico. A cross-sectional study was conducted with 83 children (5-12 years of age) residents of Villa de Reyes, SLP. Exposure to arsenic, cadmium, chromium, fluoride and lead was assessed in urine, blood and drinking water samples. Almost all tap and well water samples had levels of arsenic (81.5%) and fluoride (100%) above the permissible levels recommended by the World Health Organization. Mean urine arsenic (45.6ppb) and chromium (61.7ppb) were higher than the biological exposure index, a reference value in occupational settings. Using multivariate adjusted models, we found a dose-dependent association between kidney injury molecule-1 (KIM-1) across chromium exposure tertiles [(T1: reference, T2: 467pg/mL; T3: 615pg/mL) (p-trend=0.001)]. Chromium upper tertile was also associated with higher urinary miR-200c (500 copies/μl) and miR-423 (189 copies/μL). Arsenic upper tertile was also associated with higher urinary KIM-1 (372pg/mL). Other kidney injury/functional biomarkers such as serum creatinine, glomerular filtration rate, albuminuria, neutrophil gelatinase-associated lipocalin and miR-21 did not show any association with arsenic, chromium or any of the other toxicants evaluated. We conclude that KIM-1 might serve as a sensitive biomarker to screen children for kidney damage induced by environmental toxic agents. Copyright © 2016 Elsevier Inc. All rights reserved.

Characterization of the Organic Component of Low-Molecular-Weight Chromium-Binding Substance and Its Binding of Chromium123

PubMed Central

Chen, Yuan; Watson, Heather M.; Gao, Junjie; Sinha, Sarmistha Halder; Cassady, Carolyn J.; Vincent, John B.

2011-01-01

Chromium was proposed to be an essential element over 50 y ago and was shown to have therapeutic potential in treating the symptoms of type 2 diabetes; however, its mechanism of action at a molecular level is unknown. One chromium-binding biomolecule, low-molecular weight chromium-binding substance (LMWCr or chromodulin), has been found to be biologically active in in vitro assays and proposed as a potential candidate for the in vivo biologically active form of chromium. Characterization of the organic component of LMWCr has proven difficult. Treating bovine LMWCr with trifluoroacetic acid followed by purification on a graphite powder micro-column generates a heptapeptide fragment of LMWCr. The peptide sequence of the fragment was analyzed by MS and tandem MS (MS/MS and MS/MS/MS) using collision-induced dissociation and post-source decay. Two candidate sequences, pEEEEGDD and pEEEGEDD (where pE is pyroglutamate), were identified from the MS/MS experiments; additional tandem MS suggests the sequence is pEEEEGDD. The N-terminal glutamate residues explain the inability to sequence LMWCr by the Edman method. Langmuir isotherms and Hill plots were used to analyze the binding constants of chromic ions to synthetic peptides similar in composition to apoLMWCr. The sequence pEEEEGDD was found to bind 4 chromic ions per peptide with nearly identical cooperativity and binding constants to those of apoLMWCr. This work should lead to further studies elucidating or eliminating a potential role for LMWCr in treating the symptoms of type 2 diabetes and other conditions resulting from improper carbohydrate and lipid metabolism. PMID:21593351

Environmental Exposure to Arsenic and Chromium in Children is Associated with Kidney Injury Molecule-1

PubMed Central

Cárdenas-González, M; Osorio-Yáñez, C; Gaspar-Ramírez, O; Pavković, M; Ochoa-Martínez, A; López-Ventura, D; Medeiros, M; Barbier, OC; Pérez-Maldonado, IN; Sabbisetti, VS; Bonventre, JV; Vaidya, VS

2016-01-01

Environmental hazards from natural or anthropological sources are widespread, especially in the north-central region of Mexico. Children represent a susceptible population due to their unique routes of exposure and special vulnerabilities. In this study we evaluated the association of environmental kidney toxicants exposure and kidney injury biomarkers in children living in San Luis Potosi (SLP), Mexico. A cross-sectional study was conducted with 83 children (5-12 years of age) residents of Villa de Reyes, SLP. Exposure to arsenic, cadmium, chromium, fluoride and lead was assessed in urine, blood and drinking water samples. Almost all tap and well water samples had levels of arsenic (81.5%) and fluoride (100%) above the permissible levels recommended by the World Health Organization. Mean urine arsenic (45.6 ppb) and chromium (61.7 ppb) were higher than the biological exposure index, a reference value in occupational settings. Using multivariate adjusted models, we found a dose-dependent association between kidney injury molecule-1 (KIM-1) across chromium exposure tertiles [(T1: reference, T2: 467 pg/mL; T3: 615 pg/mL) (p-trend=0.001)]. Chromium upper tertile was also associated with higher urinary miR-200c (500 copies/μL) and miR-423 (189 copies/μL). Arsenic upper tertile was also associated with higher urinary KIM-1 (372 pg/mL). Other kidney injury/functional biomarkers such as serum creatinine, glomerular filtration rate, albuminuria, neutrophil gelatinase-associated lipocalin and miR-21 did not show any association with arsenic, chromium or any of the other toxicants evaluated. We conclude that KIM-1 might serve as a sensitive biomarker for environmental exposure risk assessment and kidney toxicity in children. PMID:27431456

Comparison of the potential for developmental toxicity of prenatal exposure to two dietary chromium supplements, chromium picolinate and [Cr3O(O2CCH2CH3)(6(H2O)3]+, in mice.

PubMed

Bailey, M M; Sturdivant, J; Jernigan, P L; Townsend, M B; Bushman, J; Ankareddi, I; Rasco, J F; Hood, R D; Vincent, J B

2008-02-01

Chromium(III) is generally thought to be an essential trace element that allows for proper glucose metabolism. However, chromium(III) picolinate, Cr(pic)3, a popular dietary supplement form of chromium, has been shown to be capable of generating hydroxyl radicals and oxidative DNA damage in rats. The cation [Cr3O(O2CCH2CH3)(6(H2O)3]+, Cr3, has been studied as an alternative supplemental source of chromium. It has been shown to increase insulin sensitivity and lower glycated hemoglobin levels in rats, making it attractive as a potential therapeutic treatment for gestational diabetes. To date, no studies have been published regarding the safety of Cr3 supplementation to a developing fetus. From gestation days (GD) 6-17, mated CD-1 female mice were fed diets delivering either 25 mg Cr/kg/day as Cr(pic)(3), 3.3 or 26 mg Cr/kg/day as Cr3, or the diet only to determine if Cr3 could cause developmental toxicity. Dams were sacrificed on GD 17, and their litters were examined for adverse effects. No signs of maternal toxicity were observed. No decrease in fetal weight or significantly increased incidence of skeletal defects was observed in the Cr3 or Cr(pic)3 exposed fetuses compared to the controls. Maternal exposure to either Cr(pic)3 or Cr3 at the dosages employed did not appear to cause deleterious effects to the developing offspring in mice. (c) 2007 Wiley-Liss, Inc.

Effects of chromium, copper, nickel, and zinc on survival and feeding of the cladoceran Moina macrocopa

DOE Office of Scientific and Technical Information (OSTI.GOV)

Wong, C.K.

1992-10-01

Heavy metals are widely recognized as highly toxic and dangerous. Past research activities on heavy metal pollution in Hong Kong have emphasized coastal environmentals. Since the main sources of heavy metals are the discharge and spillage of wastewater from electroplating factories, concentrations of heavy metals in streams and pools near industrial areas may be higher than those in coastal waters. Electroplating wastewater in Hong Kong contains high levels of chromium, copper, nickel and zinc. The toxicity of these heavy metals to the aquatic organisms has been extensively reviewed. Toxicity information for invertebrates shows that crustaceans are among the most sensitivemore » organisms. Of the crustacean species tested, cladocerans appear to be the most susceptibile. Cladocerans are important components of many aquatic ecosystems. Despite their importance in many freshwater communities and their sensitivity to heavy metal toxicity, information on the toxicity of heavy metals to cladocerans is limited except for several Daphnia species. In Hong Kong the freshwater cladoceran Moina macrocopa occurs in small ponds and rice paddies and is mass cultured by some farmers as a high quality fish food. The objectives of this study are to determine the effects of various heavy metals on the survival and feeding of M. macrocopa. 12 refs., 2 figs., 1 tab.« less

40 CFR 471.35 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... metal powder atomized Chromium 0.970 0.393 Nickel 1.44 0.970 Fluoride 156 69.2 (q) Annealing and... of process wastewater pollutant. (r) Wet Air Pollution Control Scrubber Blowdown. Subpart C—PSNS...

40 CFR 471.94 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2013 CFR

2013-07-01

... I—PSES. There shall be no discharge of process wastewater pollutants. (p) Molten salt rinse. Subpart... (pounds per million off-pounds) of zirconium-hafnium treated with molten salt Chromium 0.333 0.136 Cyanide...

40 CFR 471.93 - New source performance standards (NSPS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... of process wastewater pollutants (p) Molten salt rinse. Subpart I—NSPS Pollutant or pollutant... zirconium-hafnium treated with molten salt Chromium 0.333 0.136 Cyanide 0.220 0.091 Nickel 1.45 0.960...

40 CFR 471.94 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2014 CFR

2014-07-01

... I—PSES. There shall be no discharge of process wastewater pollutants. (p) Molten salt rinse. Subpart... (pounds per million off-pounds) of zirconium-hafnium treated with molten salt Chromium 0.333 0.136 Cyanide...

40 CFR 471.93 - New source performance standards (NSPS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... of process wastewater pollutants (p) Molten salt rinse. Subpart I—NSPS Pollutant or pollutant... zirconium-hafnium treated with molten salt Chromium 0.333 0.136 Cyanide 0.220 0.091 Nickel 1.45 0.960...

40 CFR 471.94 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2012 CFR

2012-07-01

... I—PSES. There shall be no discharge of process wastewater pollutants. (p) Molten salt rinse. Subpart... (pounds per million off-pounds) of zirconium-hafnium treated with molten salt Chromium 0.333 0.136 Cyanide...

40 CFR 471.93 - New source performance standards (NSPS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... of process wastewater pollutants (p) Molten salt rinse. Subpart I—NSPS Pollutant or pollutant... zirconium-hafnium treated with molten salt Chromium 0.333 0.136 Cyanide 0.220 0.091 Nickel 1.45 0.960...

Preliminary X-ray crystallographic analysis of SMU.573, a putative sugar kinase from Streptococcus mutans

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zhou, Yan-Feng; Li, Lan-Fen; Yang, Cheng

2008-01-01

SMU.573 from S. mutans was expressed in E. coli and crystallized. The crystals belong to space group I4 and 2.5 Å resolution diffraction data were collected at an in-house chromium radiation source. SMU.573 from Streptococcus mutans is a structurally and functionally uncharacterized protein that was selected for structural biology studies. Native and SeMet-labelled proteins were expressed with an N-His tag in Escherichia coli BL21 (DE3) and purified by Ni{sup 2+}-chelating and size-exclusion chromatography. Crystals of the SeMet-labelled protein were obtained by the hanging-drop vapour-diffusion method and a 2.5 Å resolution diffraction data set was collected using an in-house chromium radiationmore » source. The crystals belong to space group I4, with unit-cell parameters a = b = 96.53, c = 56.26 Å, α = β = γ = 90°.« less

The use of an ion-beam source to alter the surface morphology of biological implant materials

NASA Technical Reports Server (NTRS)

Weigand, A. J.

1978-01-01

An electron-bombardment ion-thruster was used as a neutralized-ion-beam sputtering source to texture the surfaces of biological implant materials. The materials investigated included 316 stainless steel; titanium-6% aluminum, 4% vanadium; cobalt-20% chromium, 15% tungsten; cobalt-35% nickel, 20% chromium, 10% molybdenum; polytetrafluoroethylene; polyoxymethylene; silicone and polyurethane copolymer; 32%-carbon-impregnated polyolefin; segmented polyurethane; silicone rubber; and alumina. Scanning electron microscopy was used to determine surface morphology changes of all materials after ion-texturing. Electron spectroscopy for chemical analysis was used to determine the effects of ion-texturing on the surface chemical composition of some polymers. Liquid contact angle data were obtained for ion-textured and untextured polymer samples. Results of tensile and fatigue tests of ion-textured metal alloys are presented. Preliminary data of tissue response to ion-textured surfaces of some metals, polytetrafluoroethylene, alumina, and segmented polyurethane have been obtained.

Removal of organic dyes using Cr-containing activated carbon prepared from leather waste.

PubMed

Oliveira, Luiz C A; Coura, Camila Van Zanten; Guimarães, Iara R; Gonçalves, Maraisa

2011-09-15

In this work, hydrogen peroxide decomposition and oxidation of organics in aqueous medium were studied in the presence of activated carbon prepared from wet blue leather waste. The wet blue leather waste, after controlled pyrolysis under CO(2) flow, was transformed into chromium-containing activated carbons. The carbon with Cr showed high microporous surface area (up to 889 m(2)g(-1)). Moreover, the obtained carbon was impregnated with nanoparticles of chromium oxide from the wet blue leather. The chromium oxide was nanodispersed on the activated carbon, and the particle size increased with the activation time. It is proposed that these chromium species on the carbon can activate H(2)O(2) to generate HO radicals, which can lead to two competitive reactions, i.e. the hydrogen peroxide decomposition or the oxidation of organics in water. In fact, in this work we observed that activated carbon obtained from leather waste presented high removal of methylene blue dye combining the adsorption and oxidation processes. Copyright © 2011 Elsevier B.V. All rights reserved.

Binder-free carbon nanotube electrode for electrochemical removal of chromium.

PubMed

Wang, Haitao; Na, Chongzheng

2014-11-26

Electrochemical treatment of chromium-containing wastewater has the advantage of simultaneously reducing hexavalent chromium (CrVI) and reversibly adsorbing the trivalent product (CrIII), thereby minimizing the generation of waste for disposal and providing an opportunity for resource reuse. The application of electrochemical treatment of chromium is often limited by the available electrochemical surface area (ESA) of conventional electrodes with flat surfaces. Here, we report the preparation and evaluation of carbon nanotube (CNT) electrodes consisting of vertically aligned CNT arrays directly grown on stainless steel mesh (SSM). We show that the 3-D organization of CNT arrays increases ESA up to 13 times compared to SSM. The increase of ESA is correlated with the length of CNTs, consistent with a mechanism of roughness-induced ESA enhancement. The increase of ESA directly benefits CrVI reduction by proportionally accelerating reduction without compromising the electrode's ability to adsorb CrIII. Our results suggest that the rational design of electrodes with hierarchical structures represents a feasible approach to improve the performance of electrochemical treatment of contaminated water.

40 CFR 437.14 - New source performance standards (NSPS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... GUIDELINES AND STANDARDS THE CENTRALIZED WASTE TREATMENT POINT SOURCE CATEGORY Metals Treatment and Recovery....3 Metal Parameters Antimony 0.111 0.0312 Arsenic 0.0993 0.0199 Cadmium 0.782 0.163 Chromium 0.167 0.0522 Cobalt 0.182 0.0703 Copper 0.659 0.216 Lead 1.32 0.283 Mercury 0.000641 0.000246 Nickel 0.794 0...

Lead chromate detected as a source of atmospheric Pb and Cr (VI) pollution.

PubMed

Lee, Pyeong-Koo; Yu, Soonyoung; Chang, Hye Jung; Cho, Hye Young; Kang, Min-Ju; Chae, Byung-Gon

2016-10-25

Spherical black carbon aggregates were frequently observed in dust dry deposition in Daejeon, Korea. They were tens of micrometers in diameter and presented a mixture of black carbon and several mineral phases. Transmission electron microscopy (TEM) observations with energy-dispersive X-ray spectroscopy (EDS) and selected area diffraction pattern (SADP) analyses confirmed that the aggregates were compact and included significant amounts of lead chromate (PbCrO 4 ). The compositions and morphologies of the nanosized lead chromate particles suggest that they probably originated from traffic paint used in roads and were combined as discrete minerals with black carbon. Based on Pb isotope analysis and air-mass backward trajectories, the dust in Daejeon received a considerable input of anthropogenic pollutants from heavily industrialized Chinese cities, which implies that long-range transported aerosols containing PbCrO 4 were a possible source of the lead and hexavalent chromium levels in East Asia. Lead chromate should be considered to be a source of global atmospheric Pb and Cr(VI) pollution, especially given its toxicity.

Lead chromate detected as a source of atmospheric Pb and Cr (VI) pollution

NASA Astrophysics Data System (ADS)

Lee, Pyeong-Koo; Yu, Soonyoung; Chang, Hye Jung; Cho, Hye Young; Kang, Min-Ju; Chae, Byung-Gon

2016-10-01

Spherical black carbon aggregates were frequently observed in dust dry deposition in Daejeon, Korea. They were tens of micrometers in diameter and presented a mixture of black carbon and several mineral phases. Transmission electron microscopy (TEM) observations with energy-dispersive X-ray spectroscopy (EDS) and selected area diffraction pattern (SADP) analyses confirmed that the aggregates were compact and included significant amounts of lead chromate (PbCrO4). The compositions and morphologies of the nanosized lead chromate particles suggest that they probably originated from traffic paint used in roads and were combined as discrete minerals with black carbon. Based on Pb isotope analysis and air-mass backward trajectories, the dust in Daejeon received a considerable input of anthropogenic pollutants from heavily industrialized Chinese cities, which implies that long-range transported aerosols containing PbCrO4 were a possible source of the lead and hexavalent chromium levels in East Asia. Lead chromate should be considered to be a source of global atmospheric Pb and Cr(VI) pollution, especially given its toxicity.

Lead chromate detected as a source of atmospheric Pb and Cr (VI) pollution

PubMed Central

Lee, Pyeong-Koo; Yu, Soonyoung; Chang, Hye Jung; Cho, Hye Young; Kang, Min-Ju; Chae, Byung-Gon

2016-01-01

Spherical black carbon aggregates were frequently observed in dust dry deposition in Daejeon, Korea. They were tens of micrometers in diameter and presented a mixture of black carbon and several mineral phases. Transmission electron microscopy (TEM) observations with energy-dispersive X-ray spectroscopy (EDS) and selected area diffraction pattern (SADP) analyses confirmed that the aggregates were compact and included significant amounts of lead chromate (PbCrO4). The compositions and morphologies of the nanosized lead chromate particles suggest that they probably originated from traffic paint used in roads and were combined as discrete minerals with black carbon. Based on Pb isotope analysis and air-mass backward trajectories, the dust in Daejeon received a considerable input of anthropogenic pollutants from heavily industrialized Chinese cities, which implies that long-range transported aerosols containing PbCrO4 were a possible source of the lead and hexavalent chromium levels in East Asia. Lead chromate should be considered to be a source of global atmospheric Pb and Cr(VI) pollution, especially given its toxicity. PMID:27779222

CAPSULE REPORT: HARD CHROME FUME SUPPRESSANTS & CONTROL TECHNOLOGIES

EPA Science Inventory

All existing information which includes the information extrapolated from the Hard Chrome Pollution Prevention Demonstration Project(s) and other sources derived from plating facilities and industry contacts, will be condensed and featured in this document. At least five chromium...

40 CFR 424.71 - Specialized definitions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 30 2013-07-01 2012-07-01 true Specialized definitions. 424.71 Section 424.71 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS FERROALLOY MANUFACTURING POINT SOURCE CATEGORY Electrolytic Chromium Subcategory § 424.71...

40 CFR 424.71 - Specialized definitions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 30 2012-07-01 2012-07-01 false Specialized definitions. 424.71 Section 424.71 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS FERROALLOY MANUFACTURING POINT SOURCE CATEGORY Electrolytic Chromium Subcategory § 424...

40 CFR 424.71 - Specialized definitions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 29 2014-07-01 2012-07-01 true Specialized definitions. 424.71 Section 424.71 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS FERROALLOY MANUFACTURING POINT SOURCE CATEGORY Electrolytic Chromium Subcategory § 424.71...

40 CFR 424.71 - Specialized definitions.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 28 2010-07-01 2010-07-01 true Specialized definitions. 424.71 Section 424.71 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS FERROALLOY MANUFACTURING POINT SOURCE CATEGORY Electrolytic Chromium Subcategory § 424.71...

40 CFR 424.71 - Specialized definitions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 29 2011-07-01 2009-07-01 true Specialized definitions. 424.71 Section 424.71 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS FERROALLOY MANUFACTURING POINT SOURCE CATEGORY Electrolytic Chromium Subcategory § 424.71...

Modulation in magnetic exchange interaction, core shell structure and Hopkinson's peak with chromium substitution into Ni0.75Co0.25Fe2O4 nano particles

NASA Astrophysics Data System (ADS)

Uday Bhasker, S.; Choudary, G. S. V. R. K.; Reddy, M. V. Ramana

2018-05-01

The ever growing applications and ever evolving challenges of magnetic nano particles has been motivating the researchers from various disciplines towards this area of magnetic nano particles. Cation substitutional effect on the magnetic structure of the nanoparticles forms a crucial aspect in their applications. Here the environmentally benign auto combustion method was employed to synthesize chromium substituted nickel cobalt ferrite (Ni0.75Co0.25Fe2-xCrxO4; x = 0, 0.10, 0.15) nano particles, from aqueous metal nitrate solutions. Chromium substitution has shown its effect on the structural, magnetic and electrical properties of Ni0.75Co0.25Fe2O4. Structural and phase analysis of the prepared samples show increased phase purity of ferrite sample with increasing Cr substitution. The TEM (Transmission Electron Microscope) image confirms the nano size of the particles, EDS (Energy dispersive X-ray Spectroscopy) has supported the stoichiometry of the prepared samples and FTIR (Fourier-transform infrared spectroscopic) analysis confirms the spinel structure and also suggests cation redistributions with chromium substitution. VSM (Vibrational Sample Magnetometer) is used to study the magnetic properties through magnetic hysteresis (M-H) loop and magnetic Hopkinson effect. All samples show hysteresis and show reduction in magnetic properties with increase in chromium content. The thermo magnetic study shows Hopkinson peak(s) in the magnetization vs. temperature (M-T) graph and also shows variation in the nature of Hopkinson peak with chromium substitution. Possible reasons for the changes in the nature of the peak are discussed.

Mitigation of Hexavalent Chromium in Storm Water Resulting from Demolition of Large Concrete Structure at the East Tennessee Technology Park - 12286

DOE Office of Scientific and Technical Information (OSTI.GOV)

Britto, Ronnie; Brown, Bridget; Hale, Timothy B.

American Recovery and Reinvestment Act (ARRA) funding was provided to supplement the environmental management program at several DOE sites, including the East Tennessee Technology Park (ETTP) in Oak Ridge, Tennessee. Demolition of the ETTP K-33 Building, the largest building to be demolished to date in Oak Ridge, was awarded to LSRS in FY-2010 under the ARRA program. The K-33 building was an 82 foot tall 2-story structure covering approximately 32 acres. Once this massive building was brought down to the ground, the debris was segregated and consolidated into piles of concrete rubble and steel across the remaining pad. The processmore » of demolishing the building, tracking across concrete debris with heavy equipment, and stockpiling the concrete rubble caused it to become pulverized. During and after storm events, hexavalent chromium leached from the residual cement present in the large quantities of concrete. Storm water control measures were present to preclude migration of contaminants off-site, but these control measures were not designed to control hexavalent chromium dissolved in storm water from reaching nearby receiving water. The following was implemented to mitigate hexavalent chromium in storm water: - Steel wool was distributed around K-33 site catch basins and in water pools as an initial step in addressing hexavalent chromium. - Since the piles of concrete were too massive and unsafe to tarp, they were placed into windrows in an effort to reduce total surface area. - A Hach colorimetric field meter was acquired by the K-33 project to provide realtime results of hexavalent chromium in site surface water. - Three hexavalent chromium treatment systems were installed at three separate catch basins that receive integrated storm water flow from the K-33 site. Sodium bisulfite is being used as a reducing agent for the immobilization of hexavalent chromium while also assisting in lowering pH. Concentrations initially were 310 - 474 ppb of hexavalent chromium in surface water at the out-falls that discharge to nearby receiving water. After implementation of the actions described above, concentrations of hexavalent chromium have been effectively reduced to less than 25 ppb at the out-falls. The LSRS team completed demolition of K-33 five months ahead of schedule, and debris removal was completed three months ahead of schedule. A total of 164,000 tons of steel and concrete from the building demolition, accounting for 13,000 shipments, were disposed to the EMWMF. Because of the high toxicity of hexavalent chromium at low concentrations, hexavalent chromium had to be controlled at ppb levels. Hexavalent chromium contaminant concentrations were successfully reduced by over 90% in surface water discharged from the K-33 demolition site into nearby receiving water. Initial efforts of wind-rowing debris piles and obtaining real-time hexavalent chromium measurements to focus initiatives coupled with placement of steel wool in pools or catch basins had some effectiveness. More significant reductions were obtained as the debris piles were removed/disposed in EMWMF, and treatment of surface water with sodium bisulfite in integrated manholes occurred. (authors)« less

Pilot Scale Production of Activated Carbon Spheres Using Fluidized Bed Reactor and Its Evaluation for the Removal of Hexavalent Chromium from Aqueous Solutions

NASA Astrophysics Data System (ADS)

Tripathi, Nagesh Kumar; Sathe, Manisha

2017-12-01

Large scale production of activated carbon is need of ongoing research due to its excellent adsorption capacity for removal of heavy metals from contaminated solutions. In the present study, polymeric precursor polystyrene beads [Brunauer Emmett Teller (BET) surface area, 46 m2/g; carbon content, 40.64%; crushing strength, 0.32 kg/sphere] were used to produce a new variant of activated carbon, Activated Carbon Spheres (ACS) in a pilot scale fluidized bed reactor. ACS were prepared by carbonization of polymeric precursor at 850 °C followed by activation of resultant material with steam. Prepared ACS were characterized using scanning electron microscope, CHNS analyzer, thermogravimetric analyzer, surface area analyzer and crushing strength tester. The produced ACS have 1009 m2/g BET surface area, 0.89 cm3/g total pore volume, 92.32% carbon content and 1.1 kg/sphere crushing strength with less than 1% of moisture and ash content. The ACS were also evaluated for its potential to remove hexavalent chromium [Cr(VI)] from contaminated solutions. The chromium removal is observed to be 99.1% at initial concentration 50 mg/l, pH 2, ACS dose 1 g/l, contact time 2 h, agitation 120 rpm and temperature 30 °C. Thus ACS can be used as an adsorbent material for the removal of Cr(VI) from contaminated solutions.

Pushing configuration-interaction to the limit: Towards massively parallel MCSCF calculations

DOE Office of Scientific and Technical Information (OSTI.GOV)

Vogiatzis, Konstantinos D.; Ma, Dongxia; Olsen, Jeppe

A new large-scale parallel multiconfigurational self-consistent field (MCSCF) implementation in the open-source NWChem computational chemistry code is presented. The generalized active space approach is used to partition large configuration interaction (CI) vectors and generate a sufficient number of batches that can be distributed to the available cores. Massively parallel CI calculations with large active spaces can be performed. The new parallel MCSCF implementation is tested for the chromium trimer and for an active space of 20 electrons in 20 orbitals, which can now routinely be performed. Unprecedented CI calculations with an active space of 22 electrons in 22 orbitals formore » the pentacene systems were performed and a single CI iteration calculation with an active space of 24 electrons in 24 orbitals for the chromium tetramer was possible. In conclusion, the chromium tetramer corresponds to a CI expansion of one trillion Slater determinants (914 058 513 424) and is the largest conventional CI calculation attempted up to date.« less

Nutrient, suspended sediment, and trace element loads in the Blackstone River Basin in Massachusetts and Rhode Island, 2007 to 2009

USGS Publications Warehouse

Zimmerman, Marc J.; Waldron, Marcus C.; DeSimone, Leslie A.

2015-01-01

Analysis of the representative constituents (total phosphorus, total chromium, and suspended sediment) upstream and downstream of impoundments indicated that the existing impoundments, such as Rice City Pond, can be sources of particulate contaminant loads in the Blackstone River. Loads of particulate phosphorus, particulate chromium, and suspended sediment were consistently higher downstream from Rice City Pond than upstream during high-flow events, and there was a positive, linear relation between streamflow and changes in these constituents from upstream to downstream of the impoundment. Thus, particulate contaminants were mobilized from Rice City Pond during high-flow events and transported downstream. In contrast, downstream loads of particulate phosphorus, particulate chromium, and suspended sediment were generally lower than or equal to upstream loads for the former Rockdale Pond impoundment. Sediments associated with the former impoundment at Rockdale Pond, breached in the late 1960s, did not appear to be mobilized during the high-flow events monitored during this study.

Pushing configuration-interaction to the limit: Towards massively parallel MCSCF calculations

DOE PAGES

Vogiatzis, Konstantinos D.; Ma, Dongxia; Olsen, Jeppe; ...

2017-11-14

A new large-scale parallel multiconfigurational self-consistent field (MCSCF) implementation in the open-source NWChem computational chemistry code is presented. The generalized active space approach is used to partition large configuration interaction (CI) vectors and generate a sufficient number of batches that can be distributed to the available cores. Massively parallel CI calculations with large active spaces can be performed. The new parallel MCSCF implementation is tested for the chromium trimer and for an active space of 20 electrons in 20 orbitals, which can now routinely be performed. Unprecedented CI calculations with an active space of 22 electrons in 22 orbitals formore » the pentacene systems were performed and a single CI iteration calculation with an active space of 24 electrons in 24 orbitals for the chromium tetramer was possible. In conclusion, the chromium tetramer corresponds to a CI expansion of one trillion Slater determinants (914 058 513 424) and is the largest conventional CI calculation attempted up to date.« less

Pushing configuration-interaction to the limit: Towards massively parallel MCSCF calculations

NASA Astrophysics Data System (ADS)

Vogiatzis, Konstantinos D.; Ma, Dongxia; Olsen, Jeppe; Gagliardi, Laura; de Jong, Wibe A.

2017-11-01

A new large-scale parallel multiconfigurational self-consistent field (MCSCF) implementation in the open-source NWChem computational chemistry code is presented. The generalized active space approach is used to partition large configuration interaction (CI) vectors and generate a sufficient number of batches that can be distributed to the available cores. Massively parallel CI calculations with large active spaces can be performed. The new parallel MCSCF implementation is tested for the chromium trimer and for an active space of 20 electrons in 20 orbitals, which can now routinely be performed. Unprecedented CI calculations with an active space of 22 electrons in 22 orbitals for the pentacene systems were performed and a single CI iteration calculation with an active space of 24 electrons in 24 orbitals for the chromium tetramer was possible. The chromium tetramer corresponds to a CI expansion of one trillion Slater determinants (914 058 513 424) and is the largest conventional CI calculation attempted up to date.

Persistent pollution of Warta river catchment with chromium: case study from central Poland

NASA Astrophysics Data System (ADS)

Hermanski, S.; Lukaczynski, I.; Nikiel, G.; Mizera, J.; Dulinski, M.; Kania, J.; Rozanski, K.; Szklarczyk, T.; Wachniew, P.; Witczak, S.; Zurek, A.

2012-04-01

Upper reaches of the Warta river, the third largest river in Poland, are located in a densely populated and industrialized area, with presence of heavy industry going back to the second half of the XIX century. Industrial activities include iron smelters in towns of Częstochowa and Zawiercie, large chemical plants (Rudniki and Aniolow) producing predominantly chromium compounds, paper and textile industry, as well as large number of small enterprises specialized in metal coatings (nickel and chromium). Until the 1960s all the industrial and municipal effluents in the region were discharged into the Warta river and its tributaries. Solid wastes were dumped on the surface, mostly without appropriate cover and isolation. This resulted in progressive contamination of surface waters and groundwater with heavy metals, mostly chromium. The upper reaches of the Warta river are located on top of upper Jurassic Major Groundwater Basin (MGWB 326 which is one of four most important groundwater reservoirs in Poland. Almost all potable water demands in the area (ca. 340,000 inhabitants, 800 factories and enterprises) are covered by MGWB 326 (50 deep wells with the average extraction rate of 57,000 m3/d). As the MGWB 326 is mostly phreatic, it has been recognized since long time that persistent pollution of the upper catchment of the Warta river with heavy metals may pose serious thread to quality of this important groundwater resource. In this presentation we summarize the work carried out to date, focused on characterization of the extent and understanding of the mechanisms of pollution of surface water, sediments and groundwater in MGWB 326 with chromium. Historical monitoring data of the levels of chromium in the Warta river and its tributaries are presented, supplemented by the results of measurements of Cr loads in Warta over-bank deposits and Cr levels in groundwater production wells in the area. Three conceptual models of spreading of chromium in the catchment of Warta river are considered: (i) leaching of Cr from waste dumps and its migration in local circulation systems with typical spatial scales of several hundred meters to single kilometers, (ii) migration of Cr on large distances (tens of kilometers) through regional, deep circulation systems, and (iii) hyporeic transport of Cr deposited in the past in over-bank sediments of the Warta river and its subsequent leaching to groundwater (spatial scales of several hundred meters to single kilometers). These conceptual models are evaluated on the basis of 3D regional flow and transport model, supplemented by environmental tracers data. Acknowledgements. The work was carried out as part of the GENESIS project on groundwater systems (http:/www.thegenesisproject.eu) financed by the European Commission 7FP contract 226536 and the statutory funds of the AGH University of Science and Technology (project No.11.11.140.026 and 11.11.220.01).

Isolation, identification and characterization of indigenous fungi for bioremediation of hexavalent chromium, nickel and cobalt

NASA Astrophysics Data System (ADS)

Hernahadini, Nelis; Suhandono, Sony; Choesin, Devi N.; Chaerun, Siti K.; Kadarusman, Ade

2014-03-01

Waste from nickel mining of Sorowako in South Sulawesi contains hexavalent chromium, nickel and cobalt metals in high concentration and may have a negative impact to the environment. Common waste treatment systems such as chemical treatment using a reducing reagent may still have a negative impact. Bioremediation using fungi or bacteria becomes more popular because it is an environmentally friendly alternative. The purposes of this study are to isolate and identify indigenous fungi that are resistant to heavy metals (hexavalent chromium, nickel, and cobalt) and are capable of reducing the concentration of metals in mining wastes. Ten fungal isolates were successfully isolated from the soils and pond sediments in the area of nickel mining in Sorowako. Selection of superior isolate was carried out by growing all the isolates on PDA medium, which contained all of the three metals. One superior isolate was identified to be able to grow on medium with concentrations of 6400 ppm hexavalent chromium, 200 ppm nickel and 50 ppm cobalt. Molecular identification and phylogenetic studies of the isolate using fungal PCR primers developed to amplify the ITS (internal transcribed spacer) region showed that the isolate sequence was very close to Trichoderma atroviride with 99.8% similarity. Optimum incubation time for the uptake of hexavalent chromium was 3 days, nickel and cobalt was 5 days, respectively, with an optimum pH of 4.

Void formation in INCONEL MA-754 by high temperature oxidation

NASA Astrophysics Data System (ADS)

Rosenstein, Alan H.; Tien, John K.; Nix, William D.

1986-01-01

Subsurface void formation in oxide dispersion strengthened MA-754 caused by high temperature oxidation was investigated at temperatures of 1100, 1150, and 1200 °C for times of 1, 10, 50, and 100 hours. Material exposed at 1200 °C was examined using microprobe, SEM, and optical microscopy techniques. After exposure in air at 1200 °C for 100 hours, chromium depletion by as much as 10 wt pct was observed near the surface, and voids of various sizes up to 15 µm in diameter were found to depths of 300 µm. The fraction of voids increases with exposure time and, with the exception of anomalous values near the surface, decreases with depth. The maximum area fraction of voids observed was approximately 8 pct. Correlation of the void area fraction profile with the measured chromium depletion through a diffusion analysis shows that void formation is due to vacancy injection. Similar void formation in Ni-Cr alloys without oxide dispersions suggests that void formation is not dependent upon the presence of oxide dispersions. The diffusion coefficient for chromium in MA-754 at 1200 °C was computed from microprobe data to be 4 × 10-10 cm2 per second.

Isothermal Calorimetric Observations of the Affect of Welding on Compatibility of Stainless Steels with High-Test Hydrogen Peroxide Propellant

NASA Technical Reports Server (NTRS)

Gostowski, Rudy C.

2002-01-01

Compatibility is determined by the surface area, the chemical constituency and the surface finish of a material. In this investigation exposed area is obviously not a factor as the welded samples had a slightly smaller surface than the unwelded, but were more reactive. The chemical makeup of welded CRES 316L and welded CRES 304L have been observed in the literature to change from the parent material as chromium and iron are segregated in zones. In particular, the ratio of chromium to iron in CRES 316L increased from 0.260 to 0.79 in the heat affected zone (HAZ) of the weld and to 1.52 in the weld bead itself. In CRES 304L the ratio of chromium to iron increased from 0.280 to 0.44 in the HAZ and to 0.33 in the weld bead. It is possible that the increased reactivity of the welded samples and of those welded without purge gas is due to this segregation phenomenon. Likewise the reactivity increased in keeping with the greater roughness of the welded and welded without purge gas samples. Therefore enhanced roughness may also be responsible for the increased reactivity.

Chromium and Ruthenium-Doped Zinc Oxide Thin Films for Propane Sensing Applications

PubMed Central

Gómez-Pozos, Heberto; González-Vidal, José Luis; Torres, Gonzalo Alberto; Rodríguez-Baez, Jorge; Maldonado, Arturo; de la Luz Olvera, María; Acosta, Dwight Roberto; Avendaño-Alejo, Maximino; Castañeda, Luis

2013-01-01

Chromium and ruthenium-doped zinc oxide (ZnO:Cr) and (ZnO:Ru) thin solid films were deposited on soda-lime glass substrates by the sol-gel dip-coating method. A 0.6 M solution of zinc acetate dihydrate dissolved in 2-methoxyethanol and monoethanolamine was used as basic solution. Chromium (III) acetylacetonate and Ruthenium (III) trichloride were used as doping sources. The Ru incorporation and its distribution profile into the films were proved by the SIMS technique. The morphology and structure of the films were studied by SEM microscopy and X-ray diffraction measurements, respectively. The SEM images show porous surfaces covered by small grains with different grain size, depending on the doping element, and the immersions number into the doping solutions. The sensing properties of ZnO:Cr and ZnO:Ru films in a propane (C3H8) atmosphere, as a function of the immersions number in the doping solution, have been studied in the present work. The highest sensitivity values were obtained for films doped from five immersions, 5.8 and 900, for ZnO:Cr and ZnO:Ru films, respectively. In order to evidence the catalytic effect of the chromium (Cr) and ruthenium (Ru), the sensing characteristics of undoped ZnO films are reported as well. PMID:23482091

Method of doping interconnections for electrochemical cells

DOEpatents

Pal, Uday B.; Singhal, Subhash C.; Moon, David M.; Folser, George R.

1990-01-01

A dense, electronically conductive interconnection layer 26 is bonded on a porous, tubular, electronically conductive air electrode structure 16, optionally supported by a ceramic support 22, by (A) forming a layer of oxide particles of at least one of the metals Ca, Sr, Co, Ba or Mg on a part 24 of a first surface of the air electrode 16, (B) heating the electrode structure, (C) applying a halide vapor containing at least lanthanum halide and chromium halide to the first surface and applying a source of oxygen to a second opposite surface of the air electrode so that they contact at said first surface, to cause a reaction of the oxygen and halide and cause a dense lanthanum-chromium oxide structure to grow, from the first electrode surface, between and around the oxide particles, where the metal oxide particles get incoporated into the lanthanum-chromium oxide structure as it grows thicker with time, and the metal ions in the oxide particles diffuse into the bulk of the lanthamum-chromium oxide structure, to provide a dense, top, interconnection layer 26 on top of the air electrode 16. A solid electrolyte layer 18 can be applied to the uncovered portion of the air electrode, and a fuel electrode 20 can be applied to the solid electrolyte, to provide an electrochemical cell 10.

40 CFR 61.01 - Lists of pollutants and applicability of part 61.

Code of Federal Regulations, 2010 CFR

2010-07-01

...) Chromium (50 FR 24317; June 10, 1985) Copper (52 FR 5496; Feb. 23, 1987) Epichlorohydrin (50 FR 24575; June... stationary sources by an authorized State air pollution control agency or by the Administrator of the U.S...

40 CFR 433.16 - New source performance standards (NSPS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... shall not exceed Milligrams per liter (mg/l) Cadmium (T) 0.11 0.07 Chromium (T) 2.77 1.71 Copper (T) 3... limits and the pollution control authority, the following amenable cyanide limit may apply in place of...

40 CFR 61.01 - Lists of pollutants and applicability of part 61.

Code of Federal Regulations, 2011 CFR

2011-07-01

...) Chromium (50 FR 24317; June 10, 1985) Copper (52 FR 5496; Feb. 23, 1987) Epichlorohydrin (50 FR 24575; June... stationary sources by an authorized State air pollution control agency or by the Administrator of the U.S...

40 CFR 433.16 - New source performance standards (NSPS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... shall not exceed Milligrams per liter (mg/l) Cadmium (T) 0.11 0.07 Chromium (T) 2.77 1.71 Copper (T) 3... limits and the pollution control authority, the following amenable cyanide limit may apply in place of...

21 CFR 175.105 - Adhesives.

Code of Federal Regulations, 2010 CFR

2010-04-01

...-isobutyronitrile Balata rubber Barium acetate Barium peroxide Barium sulfate Bentonite Benzene (benzol) 1,4... Chromium potassium sulfate Cobaltous acetate Coconut fatty acid amine salt of tetrachlorophenol For use as... sulfonamide Fats and oils derived from animal or vegetable sources, and the hydrogenated, sulfated, or...

21 CFR 175.105 - Adhesives.

Code of Federal Regulations, 2011 CFR

2011-04-01

...-isobutyronitrile Balata rubber Barium acetate Barium peroxide Barium sulfate Bentonite Benzene (benzol) 1,4... Chromium potassium sulfate Cobaltous acetate Coconut fatty acid amine salt of tetrachlorophenol For use as... sulfonamide Fats and oils derived from animal or vegetable sources, and the hydrogenated, sulfated, or...

Assessment of airborne heavy metal pollution in soil and lichen in the Meric-Ergene Basin, Turkey.

PubMed

Hanedar, Asude

2015-01-01

In the present study, accumulations of airborne heavy metals in lichen and soil samples were determined on the basis of pollutant source groups by conducting Zinc (Zn), Lead (Pb), Iron (Fe), Copper (Cu), Chromium (Cr), Cadmium (Cd), Arsenic (As), Cobalt (Co) and Manganese (Mn) analyses on a total of 48 samples collected in the periods of May 2014 and August 2014 from 12 sampling points in a heavily industrialized area, a mixed industrial and residential area, an agricultural area and a background area in the Meric-Ergene Basin, and pH and total organic carbon determination was carried out on soil samples. With the obtained data, heavy metal levels were statistically assessed in detail by being associated with each other and with their probable sources; the accumulations found in soil and lichen samples were compared and spatial variances were set forth. Based on the results, it was observed that heavy metal pollution is at high levels particularly in industrialized areas, and that the differences between the cleanest and most polluted levels determined from soil samples for As, Cr, Cd and Pb reach 10 folds. The highest levels of all heavy metals were determined in both the soil and lichen samples collected from the areas in the south-east part of the region, where industrial activities and particularly leather and chemical industries are concentrated. With the comparison of the indication properties of soil and lichen, it was determined that significant and comparable results can be observed in both matrices.

Method for producing high surface area chromia materials for catalysis

DOEpatents

Gash, Alexander E [Brentwood, CA; Satcher, Joe [Patterson, CA; Tillotson, Thomas [Tracy, CA; Hrubesh, Lawrence [Pleasanton, CA; Simpson, Randall [Livermore, CA

2007-05-01

Nanostructured chromium(III)-oxide-based materials using sol-gel processing and a synthetic route for producing such materials are disclosed herein. Monolithic aerogels and xerogels having surface areas between 150 m.sup.2/g and 520 m.sup.2/g have been produced. The synthetic method employs the use of stable and inexpensive hydrated-chromium(III) inorganic salts and common solvents such as water, ethanol, methanol, 1-propanol, t-butanol, 2-ethoxy ethanol, and ethylene glycol, DMSO, and dimethyl formamide. The synthesis involves the dissolution of the metal salt in a solvent followed by an addition of a proton scavenger, such as an epoxide, which induces gel formation in a timely manner. Both critical point (supercritical extraction) and atmospheric (low temperature evaporation) drying may be employed to produce monolithic aerogels and xerogels, respectively.

Chromium in urban sediment particulates: an integrated micro-chemical and XANES study

NASA Astrophysics Data System (ADS)

Taylor, Kevin; Byrne, Patrick; Hudson-Edwards, Karen

2015-04-01

Chromium is generally common within the urban sediment cascade as a result of abundant industrial and transport-related sources. The risks that Cr-bearing particles pose to ecosystems and humans depend on the solid phase chemical speciation of Cr in the particles. In this study, we use bulk chemical digests, sequential chemical extraction analysis, electron microscopy, electron microprobe and microfocus XANES analysis to describe the solid-phase speciation of Cr in urban particulate matter from both aquatic sediment and road dust sediment (RDS) in Manchester, UK. Cr-bearing grains within RDS are predominantly iron oxide grains, commonly of goethite or haematite mineralogy, but Cr-bearing silicate glass grains are also present. Iron oxide glass grains most likely have sorbed Cr, and derive from the rusting of Cr-steel particles from vehicles. Electron microprobe analysis indicates concentrations of Cr up to 3200 μg/g in these grains, and XANES analysis indicates that Cr(III) is the dominant oxidation state, with some trace amounts of Cr(VI). Cr-bearing grains within aquatic sediments are dominated by alumino-silicate glass grains derived from industrial waste. These grains contain Cr-rich areas with up to 19% Cr2O3 and XANES analysis indicates that Cr is present as Cr(III). The dominance of Cr(III) in these urban particulate grains suggests limited bioavailability or toxicity. However, the presence within two markedly different grain types (iron oxides and silicate glasses) indicates that the long-term geochemical behaviour and environmental risk of RDS and the aquatic sediments studied are likely to be quite different. These findings highlight the importance of understanding sources of metal contaminants in urban environments and the geochemical processes that affect their transfer through the urban sediment cascade and the wider river basin.

NORTH FORK SMITH RIVER ROADLESS AREA, CALIFORNIA AND OREGON.

USGS Publications Warehouse

Gray, Floyd; Hamilton, Michael

1984-01-01

Geologic, geochemical, and geophysical investigations and a survey of mines and prospects were conducted to evaluate the mineral-resource potential of the North Fork Smith River Roadless Area, California. The area has probable and sustantiated resource potential for nickel, chromium, copper, and mercury and approximately 2300 mining claims exist in or adjacent to the area. The geologic terrane precludes the occurrence of fossil fuel resources.

E-cigarettes as a source of toxic and potentially carcinogenic metals

DOE Office of Scientific and Technical Information (OSTI.GOV)

Hess, Catherine Ann, E-mail: chess@prev.org

Background and aims: The popularity of electronic cigarette devices is growing worldwide. The health impact of e-cigarette use, however, remains unclear. E-cigarettes are marketed as a safer alternative to cigarettes. The aim of this research was the characterization and quantification of toxic metal concentrations in five, nationally popular brands of cig-a-like e-cigarettes. Methods: We analyzed the cartomizer liquid in 10 cartomizer refills for each of five brands by Inductively Coupled Plasma Mass Spectrometry (ICP-MS). Results: All of the tested metals (cadmium, chromium, lead, manganese and nickel) were found in the e-liquids analyzed. Across all analyzed brands, mean (SD) concentrations rangedmore » from 4.89 (0.893) to 1970 (1540) μg/L for lead, 53.9 (6.95) to 2110 (5220) μg/L for chromium and 58.7 (22.4) to 22,600 (24,400) μg/L for nickel. Manganese concentrations ranged from 28.7 (9.79) to 6910.2 (12,200) μg/L. We found marked variability in nickel and chromium concentration within and between brands, which may come from heating elements. Conclusion: Additional research is needed to evaluate whether e-cigarettes represent a relevant exposure pathway for toxic metals in users. - Highlights: • Certain brands of cig-a-like e-cigarettes contain high levels of nickel and chromium. • Cig-a-likes contain low levels of cadmium, compared to tobacco cigarettes. • Nickel and chromium in the e-liquid of cig-a-likes may come from nichrome heating coils.« less

Phytoremediation of industrial mines wastewater using water hyacinth.

PubMed

Saha, Priyanka; Shinde, Omkar; Sarkar, Supriya

2017-01-02

The wastewater at Sukinda chromite mines (SCM) area of Orissa (India) showed high levels of toxic hexavalent chromium (Cr VI). Wastewater from chromium-contaminated mines exhibit potential threats for biotic community in the vicinity. The aim of the present investigation is to develop a suitable phytoremediation technology for the effective removal of toxic hexavalent chromium from mines wastewater. A water hyacinth species Eichhornia crassipes was chosen to remediate the problem of Cr (VI) pollution from wastewater. It has been observed that this plant was able to remove 99.5% Cr (VI) of the processed water of SCM in 15 days. This aquatic plant not only removed hexavalent Cr, but is also capable of reducing total dissolved solids (TDS), biological oxygen demand (BOD), chemical oxygen demand (COD), and other elements of water also. Large-scale experiment was also performed using 100 L of water from SCM and the same removal efficiency was achieved.

Phytoremediation of industrial mines wastewater using water hyacinth

PubMed Central

Saha, Priyanka; Shinde, Omkar; Sarkar, Supriya

2017-01-01

ABSTRACT The wastewater at Sukinda chromite mines (SCM) area of Orissa (India) showed high levels of toxic hexavalent chromium (Cr VI). Wastewater from chromium-contaminated mines exhibit potential threats for biotic community in the vicinity. The aim of the present investigation is to develop a suitable phytoremediation technology for the effective removal of toxic hexavalent chromium from mines wastewater. A water hyacinth species Eichhornia crassipes was chosen to remediate the problem of Cr (VI) pollution from wastewater. It has been observed that this plant was able to remove 99.5% Cr (VI) of the processed water of SCM in 15 days. This aquatic plant not only removed hexavalent Cr, but is also capable of reducing total dissolved solids (TDS), biological oxygen demand (BOD), chemical oxygen demand (COD), and other elements of water also. Large-scale experiment was also performed using 100 L of water from SCM and the same removal efficiency was achieved. PMID:27551860

Chromium Isotopes in Carbonates - a Tracer for Climate Change and for Reconstructing the Redox state of Ancient Seawater

NASA Astrophysics Data System (ADS)

Frei, R.; Gaucher, C.; Dossing, L. N.; Sial, A. N.

2011-12-01

Strontium and carbon isotopes of marine carbonates are routinely applied for chemostratigraphic cross correlations of time-equivalent sedimentary sequences and for calibration of the compositional evolution of seawater throughout Earth's history, mainly for the purpose of reconstructing ancient climatic changes. We here present results of a new isotopic tracer system - stable chromium isotopes - applied to a late Ediacaran (Vendian) marine carbonate sequence exposed in the Calera de Recalde syncline, Arroyo del Soldado Group, Uruguay. The aim was to compare Cr isotope signatures directly to δ13C, 87Sr/86Sr and 143Nd/144Nd fluctuations in a well defined stratigraphic profile comprising sediments that were deposited during cold-warm periods accompanied by sea-level changes in response to glaciation-deglaciation at higher latitudes. The studied section is characterized by a pronounced negative (down to -3.3%) δ13C excursion in carbonates paralleled by a decrease of 87Sr/86Sr values. Chromium isotope signatures over this section also show a correlated decrease in δ53Cr (δ53Cr = [(53Cr/52Cr)sample/(53Cr/52Cr)SRM979)-1] x 1000) values from ~+0.29to -0.17% which mirrors a decrease in positively fractioned seawater signatures to slightly negative values characteristic of high-temperature magmatic sources. Linear correlations between δ53Cr and ɛNd(T=570 Ma), 87Sr/86Sr and Cr concentrations can be explained by mixing between two major input sources of Cr, Nd and Sr into the shallow seawater: 1) a source characterized by negative δ53Cr values of ~-0.2% , low 87Sr/86Sr values of ~0.707, and elevated 147Sm/144Nd values of ~0.13, recognized as a subaqueous hydrothermal dominated input source, and 2) a source characterized by positively fractionated δ53Cr values of ~+0.2%, higher 87Sr/86Sr values of ~0.708, and lower 147Sm/144Nd values of ~0.11, a source which is strongly affected by continentally derived input. Chromium isotopes provide a powerful tool for reconstructing the redox state of ancient seawater since positive values indicate that, at least locally, Neoproterozoic shallow ocean waters were sufficiently oxidized to fractionate chromium and/or that oxygen levels of the atmosphere were sufficient to transform Cr(III) into the more mobile hexavalent Cr(VI) formed during weathering processes on land. The fact that 87Sr/86Sr values, despite δ13C fluctuations, remain low (indicative of a strong hydrothermal input into the basin at his time) implies that CO2 limitation was the cause of negative δ13C and δ53Cr excursions in otherwise nutrient rich late Vendian basins, and that glaciation is only one more consequence of a tectonically driven, biologically mediated system. In such a scenario, glaciation acts as an amplifier of δ53Cr signals. These signals in marine carbonates are a sensitive tracer for redox processes in the ocean and/or on land and have the potential to contribute significantly to the reconstruction of climatic changes, particularly those that are associated with major glaciation periods in Earth's history.

40 CFR 467.62 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2011 CFR

2011-07-01

... (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions... off-lbs) of aluminum drawn with emulsions or soaps Chromium 0.205 0.084 Cyanide 0.135 0.056 Zinc 0.680...

40 CFR 467.62 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions... off-lbs) of aluminum drawn with emulsions or soaps Chromium 0.205 0.084 Cyanide 0.135 0.056 Zinc 0.680...

40 CFR 467.22 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions...-lbs) of aluminum rolled with emulsions Chromium 0.057 0.024 Cyanide 0.038 0.016 Zinc 0.19 0.079...

40 CFR 467.22 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2011 CFR

2011-07-01

... (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions...-lbs) of aluminum rolled with emulsions Chromium 0.057 0.024 Cyanide 0.038 0.016 Zinc 0.19 0.079...

40 CFR 467.63 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2012 CFR

2012-07-01

...) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions...-lbs) of aluminum drawn with emulsions or soaps Chromium 0.205 0.084 Cyanide 0.135 0.056 Zinc 0.681 0...

40 CFR 467.63 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2014 CFR

2014-07-01

...) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions...-lbs) of aluminum drawn with emulsions or soaps Chromium 0.205 0.084 Cyanide 0.135 0.056 Zinc 0.681 0...

40 CFR 424.74-424.76 - [Reserved

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 30 2012-07-01 2012-07-01 false [Reserved] 424.74-424.76 Section 424.74-424.76 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS FERROALLOY MANUFACTURING POINT SOURCE CATEGORY Electrolytic Chromium Subcategory §§ 424...

A Comparison of Blood Metal Ions in Total Hip Arthroplasty Using Metal and Ceramic Heads.

PubMed

White, Peter B; Meftah, Morteza; Ranawat, Amar S; Ranawat, Chitranjan S

2016-10-01

In recent time, metal ion debris and adverse local tissue reaction have reemerged as an area of clinical concern with the use of large femoral heads after total hip arthroplasty (THA). Between June 2014 and January 2015, 60 patients with a noncemented THA using a titanium (titanium, molybdenum, zirconium, and iron alloy) femoral stem and a V40 trunnion were identified with a minimum 5-year follow-up. All THAs had a 32- or 36-mm metal (n = 30) or ceramic (n = 30) femoral head coupled with highly cross-linked polyethylene. Cobalt, chromium, and nickel ions were measured. Patients with metal heads had detectable cobalt and chromium levels. Cobalt levels were detectable in 17 (56.7%) patients with a mean of 2.0 μg/L (range: <1.0-10.8 μg/L). Chromium levels were detectable in 5 (16.7%) patients with a mean of 0.3 μg/L (range: <1.0-2.2 μg/L). All patients with a ceramic head had nondetectable cobalt and chromium levels. Cobalt and chromium levels were significantly higher with metal heads compared to ceramic heads (P < .01). Cobalt levels were significantly higher with 36-mm metal heads compared with 32-mm heads (P < .01). Seven patients with metal femoral heads had mild hip symptoms, 4 of whom had positive findings of early adverse local tissue reaction on magnetic resonance imaging. All ceramic THA was asymptomatic. The incidence and magnitude of cobalt and chromium levels is higher in metal heads compared to ceramic heads with this implant system (P < .01). Thirty-six millimeter metal femoral heads result in larger levels of cobalt compared with 32-mm metal heads. Copyright © 2016 Elsevier Inc. All rights reserved.

Method for the determination of chromium in feed matrix by HPLC.

PubMed

Umesh, Balakrishnan; Rajendran, Rajendra Moorthy; Manoharan, Muthu Tamizh

2015-11-01

An improved method for the chromatographic separation and determination of chromium (III) and (VI) [ CRIII AND CRVI: ] in mineral mixtures and feed samples has been developed. The method uses precolumn derivatization using ammonium pyrrolidinedithiocarbamate ( APD: ) followed by reversed-phase liquid chromatography to separate the chromium ions. Both Cr(III) and Cr(VI) species are chelated with ammonium pyrrolidinedithiocarbamate prior to separation by mixing with acetonitrile and 0.5 mmol acetate buffer (pH 4.5). Optimum chromatographic separations were obtained with a polymer-based reversed-phase column (Kinetex, 5 μ, 250 × 4.5 mm, Phenomenex, Torrance, CA) and a mobile phase containing acetonitrile and water (7:3). Both Cr(III) and Cr(VI) ion concentrations were directly determined from the corresponding areas in the chromatogram. The effect of analytical parameters, including pH, concentration of ligand, incubation temperature, and mobile phase, was optimized for both chromium complexes. The range of the procedure was found to be linear for Cr(III) and Cr(VI) concentrations between 0.125 and 4 μg/mL (r² = 0.9926) and 0.1 and 3.0 μg/mL (r² = 0.9983), respectively. Precision was evaluated by replicate analysis in which the percentage relative standard deviation values for chromium complex were found to be below 4.0. The recoveries obtained (85-115%) for both Cr(III) and Cr(VI) complexes indicated the accuracy of the developed method. The degradation products, as well as the excipients, were well resolved from the chromium complex peak in the chromatogram. Finally, the new method proved to be suitable for routine analysis of Cr(III) and Cr(VI) species in raw materials, mineral mixtures, and feed samples. © 2015 Poultry Science Association Inc.

[Comparison of magnetic resonance imaging artifacts of five common dental materials].

PubMed

Xu, Yisheng; Yu, Risheng

2015-06-01

To compare five materials commonly used in dentistry, including three types of metals and two types of ceramics, by using different sequences of three magnetic resonance imaging (MRI) field strengths (0.35, 1.5, and 3.0 T). Three types of metals and two types of ceramics that were fabricated into the same size and thickness as an incisor crown were placed in a plastic tank filled with saline. The crowns were scanned using an magnetic resonance (MR) machine at 0.35, 1.5, and 3.0 T field strengths. The TlWI and T2WI images were obtained. The differences of various materials in different artifacts of field MR scans were determined. The zirconia crown presented no significant artifacts when scanned under the three types of MRI field strengths. The artifacts of casting ceramic were minimal. All dental precious metal alloys, nickel-chromium alloy dental porcelain, and cobalt-chromium ceramic alloy showed varying degrees of artifacts under the three MRI field strengths. Zirconia and casting ceramics present almost no or faint artifacts. By contrast, precious metal alloys, nickel-chromium alloy dental porcelain and cobalt-chromium ceramic alloy display MRI artifacts. The artifact area increase with increasing magnetic field.

Callitriche cophocarpa biomass as a potential low-cost biosorbent for trivalent chromium.

PubMed

Kyzioł-Komosińska, Joanna; Augustynowicz, Joanna; Lasek, Wojciech; Czupioł, Justyna; Ociński, Daniel

2018-05-15

The present study focused on the use of the dry mass of the macrophyte Callitriche cophocarpa as an effective biosorbent for chromium removal from concentrated solutions, typical for industrial effluents. In order to evaluate the usability of C. cophocarpa as the Cr(III) sorbent, its detailed physicochemical characterization has been performed as well as the preliminary adsorption studies. The biosorbent was characterized by specific surface area (SSA), porosity, total organic carbon (TOC), inorganic content as well as the cation exchange capacity (CEC), dominant exchangeable cations and anion exchange capacity (AEC), point of zero charge (pH pzc ) and buffering capacity. The effect of the initial chromium concentration, solution pH and co-existing anions on the sorption effectiveness have been investigated. Based on theoretical isotherm models, the maximum adsorption capacity of the dry C. cophocarpa has been determined as 77.1 mg Cr(III)/g. Finally, the strength of Cr-binding onto the plant biomass has been evaluated using the BCR extraction method, stating that chromium was strongly and - under environmental conditions - irreversibly bound to the plant biomass. Copyright © 2018 Elsevier Ltd. All rights reserved.

Adsorption Studies of Chromium(VI) on Activated Carbon Derived from Mangifera indica (Mango) Seed Shell

NASA Astrophysics Data System (ADS)

Mise, Shashikant; Patil, Trupti Nagendra

2015-09-01

The removal of chromium(VI) from synthetic sample by adsorption on activated carbon prepared from Mangifera indica (mango) seed shell have been carried out at room temperature 32 ± 1 °C. The removal of chromium(VI) from synthetic sample by adsorption on two types of activated carbon, physical activation and chemical activation (Calcium chloride and Sodium chloride), Impregnation Ratio's (IR) 0.25, 0.50, 0.75 for optimum time, optimum dosages and variation of pH were studied. It is observed that contact time differs for different carbons i.e. for physically and chemically activated carbons. The contact time decreases for chemically activated carbon compared to the physically activated carbon. It was observed that as dosage increases the adsorption increased along with the increase in impregnation ratio. It was also noted that as I.R. increases the surface area of Mangifera indica shell carbon increased. These dosage data were considered in the construction of isotherms and it was found that adsorption obeys Freundlich Isotherm and does not obey Langmuir Isotherm. The maximum removal of chromium (VI) was obtained in highly acidic medium at a pH of 1.50.

Immobilization of Cr6+ in an urban and industrial soil from Mexico

NASA Astrophysics Data System (ADS)

Jordán, Manuel Miguel; Ballesteros, Sergio; María Rincón, Jesus; Rincón-Mora, Beatriz; Pardo, Francisco; Bech, Jaume

2017-04-01

In Mexico, some areas are highly contaminated by heavy metals. Currently, there are more than 75,000 tons of untreated residues in the form of slags and sludges containing high concentrations of hexavalent chromium, Cr6+, in densely populated zones very near Mexico City. Capillary migration of Cr6+ and its concentration towards the surface at landfill or confinement sites is variable due to the presence of slowly soluble chromium salts and changes in meteorological conditions. Due to these phenomena, concentrations a few centimeters from the ground surface can vary from just a few parts per million to percentage levels that are many times greater than the concentration at the very confinement site. At these sites, chromate enrichment is evident at the subsoil surface or confinement areas as outcrops in the form of greenish-yellow stains extending along constructed walls and confinement installations or processing areas. This research describes the characteristics, formation mechanisms, and leaching of Cr6+ wastes that are contaminating a Mexican urban soil (Ballesteros et al, 2016). By means of a vitrification process, a method has been proposed that transforms Cr6+ to Cr3+ and achieves effective immobilization of this highly toxic industrial waste affecting an urban area. By various physicochemical techniques, such as XRD, DTA, and SEM/EDS, carrying out complete characterization of these new materials was possible. The final vitrified or glassy products of silicate composition lead to a glass ceramic material that is environmentally very stable, showing high chemical and mechanical stability where all Cr6+ was reduced to Cr3+ in the residual glass network, as well as other chromium oxidation states confined in the crystalline phases formed in the final glass-ceramic. The leaching tests on samples stabilized by vitrification have shown that the release of ions from the structure of these new materials was negligible, yielding values less than 0.5 mg/l with respect to current international and domestic environmental regulations. References Ballesteros; S, Rincón, J.Ma; Rincón-Mora, B.; Jordán, M.M. (2016). Vitrification of Urban Soil Contamination by Hexavalent Chromium. Journal of Geochemical Exploration. In press.

Occurrence of hexavalent chromium in ground water in the western Mojave Desert, California

USGS Publications Warehouse

Ball, J.W.; Izbicki, J.A.

2004-01-01

About 200 samples from selected public supply, domestic, and observation wells completed in alluvial aquifers underlying the western Mojave Desert were analyzed for total dissolved Cr and Cr(VI). Because Cr(VI) is difficult to preserve, samples were analyzed by 3 methods. Chromium(VI) was determined in the field using both a direct colorimetric method and EPA method 218.6, and samples were speciated in the field for later analysis in the laboratory using a cation-exchange method developed for the study described in this paper. Comparison of the direct colorimetric method and EPA method 218.6 with the new cation-exchange method yielded r2 values of 0.9991 and 0.9992, respectively. Total dissolved Cr concentrations ranged from less than the 0.1 ??g/l detection limit to 60 ??g/l, and almost all the Cr present was Cr(VI). Near recharge areas along the mountain front pH values were near neutral, dissolved O2 concentrations were near saturation, and Cr(VI) concentrations were less than the 0.1 ??g/l detection limit. Chromium(VI) concentrations and pH values increased downgradient as long as dissolved O 2 was present. However, low Cr(VI) concentrations were associated with low dissolved O2 concentrations near ground-water discharge areas along dry lakes. Chromium(VI) concentrations as high as 60 ??g/l occurred in ground water from the Sheep Creek fan alluvial deposits weathered from mafic rock derived from the San Gabriel Mountains, and Cr(VI) concentrations as high as about 36 ??g/l were present in ground water from alluvial deposits weathered from less mafic granitic, metamorphic, and volcanic rocks. Chromium(III) was the predominant form of Cr only in areas where dissolved O2 concentrations were less than 1 mg/l and was detected at a median concentration of 0.1 ??g/l, owing to its low solubility in water of near-neutral pH. Depending on local hydrogeologic conditions and the distribution of dissolved O2, Cr(VI) concentrations may vary considerably with depth. Samples collected under pumping conditions from different depths within wells show that Cr(VI) concentrations can range from less than the 0.1 ??g/l detection limit to 36 ??g/l in a single well and that dissolved O2 concentrations likely control the concentration and redox speciation of Cr in ground water.

Elemental speciation for chromium in chromium picolinate products

NASA Astrophysics Data System (ADS)

Ding, Hong; Olson, Lisa K.; Caruso, Joseph A.

1996-12-01

Chromium picolinate products have been examined for different forms of chromium, using chromatographic separation and inductively coupled plasma mass spectrometric detection. The brands we evaluated contained no detectable amount of elemental chromium(VI), the toxic form. Since chromium picolinate might have other chromium forms as impurities, different products may contain different forms of chromium species. Compared with ion-exchange, reversed-phase chromatography showed excellent chromium recovery based on the amount stated on the product label.

Annual and seasonal variability of metals and metalloids in urban and industrial soils in Alcalá de Henares (Spain).

PubMed

Peña-Fernández, A; Lobo-Bedmar, M C; González-Muñoz, M J

2015-01-01

Contamination of urban and industrial soils with trace metals has been recognized as a major concern at local, regional and global levels due to their implication on human health. In this study, concentrations of aluminum (Al), arsenic (As), beryllium (Be), cadmium (Cd), chromium (Cr), manganese (Mn), nickel (Ni), lead (Pb), tin (Sn), thallium (Tl), vanadium (V) and zinc (Zn) were determined in soil samples collected in Alcalá de Henares (Madrid, Spain) in order to evaluate the annual and seasonal variation in their levels. The results show that the soils of the industrial area have higher metals concentrations than the urban area. Principal component analysis (PCA) revealed that the two principal sources of trace metal contamination, especially Cd, Cu, Pb, and Zn in the urban soils of Alcalá can be attributed to traffic emissions, while As, Ni and Be primarily originated from industrial discharges. The seasonal variation analysis has revealed that the emission sources in the industrial area remain constant with time. However, in urban areas, both emissions and emission pathways significantly increase over time due to ongoing development. Currently, there is no hypothesis that explains the small seasonal fluctuations of trace metals in soils, since there are many factors affecting this. Owing to the fact that urban environments are becoming the human habitat, it would therefore be advisable to monitor metals and metalloids in urban soils because of the potential risks to human health. Copyright © 2014 Elsevier Inc. All rights reserved.

Remediation of ground water containing volatile organic compounds and tritium

DOE Office of Scientific and Technical Information (OSTI.GOV)

Shukla, S.N.; Folsom, E.N.

1994-03-01

The Trailer 5475 (T-5475) East Taxi Strip Area at Lawrence Livermore National Laboratory (LLNL), Livermore, California was used as a taxi strip by the US Navy to taxi airplanes to the runway from 1942 to 1947. Solvents were used in some unpaved areas adjacent to the East Taxi Strip for cleaning airplanes. From 1953 through 1976, the area was used to store and treat liquid waste. From 1962 to 1976 ponds were constructed and used for evaporation of liquid waste. As a result, the ground water in this area contains volatile organic compounds (VOCs) and tritium. The ground water inmore » this area is also known to contain hexavalent chromium that is probably naturally occurring. Therefore, LLNL has proposed ``pump-and-treat`` technology above grade in a completely closed loop system. The facility will be designed to remove the VOCs and hexavalent chromium, if any, from the ground water, and the treated ground water containing tritium will be reinjected where it will decay naturally in the subsurface. Ground water containing tritium will be reinjected into areas with equal or higher tritium concentrations to comply with California regulations.« less

Type 2 Diabetic Rats on Diet Supplemented With Chromium Malate Show Improved Glycometabolism, Glycometabolism-Related Enzyme Levels and Lipid Metabolism

PubMed Central

Feng, Weiwei; Zhao, Ting; Mao, Guanghua; Wang, Wei; Feng, Yun; Li, Fang; Zheng, Daheng; Wu, Huiyu; Jin, Dun; Yang, Liuqing; Wu, Xiangyang

2015-01-01

Our previous study showed that chromium malate improved the regulation of blood glucose in mice with alloxan-induced diabetes. The present study was designed to evaluate the effect of chromium malate on glycometabolism, glycometabolism-related enzymes and lipid metabolism in type 2 diabetic rats. Our results showed that fasting blood glucose, serum insulin level, insulin resistance index and C-peptide level in the high dose group had a significant downward trend when compared with the model group, chromium picolinate group and chromium trichloride group. The hepatic glycogen, glucose-6-phosphate dehydrogenase, glucokinase, Glut4, phosphor-AMPKβ1 and Akt levels in the high dose group were significantly higher than those of the model, chromium picolinate and chromium trichloride groups. Chromium malate in a high dose group can significantly increase high density lipoprotein cholesterol level while decreasing the total cholesterol, low density lipoprotein cholesterol and triglyceride levels when compared with chromium picolinate and chromium trichloride. The serum chromium content in chromium malate and chromium picolinate group is significantly higher than that of the chromium trichloride group. The results indicated that the curative effects of chromium malate on glycometabolism, glycometabolism-related enzymes and lipid metabolism changes are better than those of chromium picolinate and chromium trichloride. Chromium malate contributes to glucose uptake and transport in order to improved glycometabolism and glycometabolism-related enzymes. PMID:25942313

Type 2 diabetic rats on diet supplemented with chromium malate show improved glycometabolism, glycometabolism-related enzyme levels and lipid metabolism.

PubMed

Feng, Weiwei; Zhao, Ting; Mao, Guanghua; Wang, Wei; Feng, Yun; Li, Fang; Zheng, Daheng; Wu, Huiyu; Jin, Dun; Yang, Liuqing; Wu, Xiangyang

2015-01-01

Our previous study showed that chromium malate improved the regulation of blood glucose in mice with alloxan-induced diabetes. The present study was designed to evaluate the effect of chromium malate on glycometabolism, glycometabolism-related enzymes and lipid metabolism in type 2 diabetic rats. Our results showed that fasting blood glucose, serum insulin level, insulin resistance index and C-peptide level in the high dose group had a significant downward trend when compared with the model group, chromium picolinate group and chromium trichloride group. The hepatic glycogen, glucose-6-phosphate dehydrogenase, glucokinase, Glut4, phosphor-AMPKβ1 and Akt levels in the high dose group were significantly higher than those of the model, chromium picolinate and chromium trichloride groups. Chromium malate in a high dose group can significantly increase high density lipoprotein cholesterol level while decreasing the total cholesterol, low density lipoprotein cholesterol and triglyceride levels when compared with chromium picolinate and chromium trichloride. The serum chromium content in chromium malate and chromium picolinate group is significantly higher than that of the chromium trichloride group. The results indicated that the curative effects of chromium malate on glycometabolism, glycometabolism-related enzymes and lipid metabolism changes are better than those of chromium picolinate and chromium trichloride. Chromium malate contributes to glucose uptake and transport in order to improved glycometabolism and glycometabolism-related enzymes.

The use of trivalent chromium bath to obtain a solar selective black chromium coating

NASA Astrophysics Data System (ADS)

Survilienė, S.; Češūnienė, A.; Juškėnas, R.; Selskienė, A.; Bučinskienė, D.; Kalinauskas, P.; Juškevičius, K.; Jurevičiūtė, I.

2014-06-01

Black chromium coatings were electrodeposited from a trivalent chromium bath using a ZnO additive as a second main component. Black chromium was electrodeposited on steel and copper plates and substrates plated with bright nickel prior to black chromium electrodeposition. The black chromium coatings were characterized by XRD and SEM. The XRD data suggest that the phase structure of black chromium may be defined as a zinc solid solution in chromium or a chromium solid solution in zinc depending on the chromium/zinc ratio in the deposit. The role of substrate finish was evaluated through the corrosion resistance and reflectance of black chromium. According to corrosion tests the samples plated with bright nickel prior to black chromium deposition have shown the highest corrosion resistance. The electrodeposited black chromium possesses good optical properties for the absorption of solar energy. The absorption coefficient of black chromium was found to be over 0.99 for the samples obtained without the Ni undercoat and below 0.99 for those obtained with the use of Ni undercoat. However, the use of nickel undercoat before black chromium plating is recommended because it remarkably improves the corrosion resistance of samples.

Simulation of ground-water flow in the Potomac-Raritan-Magothy aquifer system, Pennsauken Township and vicinity, New Jersey

USGS Publications Warehouse

Pope, Daryll A.; Watt, Martha K.

2004-01-01

The Potomac-Raritan-Magothy aquifer system is one of the primary sources of potable water in the Coastal Plain of New Jersey, particularly in heavily developed areas along the Delaware River. In Pennsauken Township, Camden County, local drinking-water supplies from this aquifer system have been contaminated by hexavalent chromium at concentrations that exceed the New Jersey maximum contaminant level. In particular, ground water at the Puchack well field has been adversely affected to the point where, since 1984, water is no longer withdrawn from this well field for public supply. The area that contains the Puchack well field was added to the National Priorities List in 1998 as a Superfund site. The U.S. Geological Survey (USGS) conducted a reconnaissance study from 1996 to 1998 during which hydrogeologic and water-quality data were collected and a ground-water-flow model was developed to describe the conditions in the aquifer system in the Pennsauken Township area. The current investigation by the USGS, in cooperation with the U.S. Environmental Protection Agency (USEPA), is an extension of the previous study. Results of the current study can be applied to a Remedial Investigation and Feasibility Study conducted at the Puchack well field Superfund site. The USGS study collected additional data on the hydrogeology and water-quality in the area. These data were incorporated into a refined model of the ground-water-flow system in the Potomac-Raritan-Magothy aquifer system. A finite-difference model was developed to simulate ground-water flow and the advective transport of chromium-contaminated ground water in the aquifers of the Potomac-Raritan-Magothy aquifer system in the Pennsauken Township area. An 11-layer model was used to represent the complex hydrogeologic framework. The model was calibrated using steady-state water-level data from March 1998, April 1998, and April 2001. Water-level recovery during the shutdown of Puchack 1 during March to April 1998 was simulated to evaluate model performance in relation to changing stresses. The Delaware River contributes appreciable-flow to the ground-water system from areas where the Middle and Lower aquifers crop out beneath the river. A transient simulation of an aquifer test near the Delaware River was run to help characterize the hydraulic conductivity of the riverbed sediments represented in the model. Vertical flow across confining units between the aquifers is highly variable and is important in the movement of water and associated contaminants through the flow system. The model was imbedded within a regional model of the Potomac-Raritan-Magothy aquifer system in Camden County. In general, a simulation of baseline conditions, which can provide a representation on which simulations of various alternatives can be based for the feasibility study, incorporated average conditions from 1998 to 2000. Ground-water withdrawals within the model area during this period averaged about 14 Mgal/d. Regional ground-water flow is from recharge areas and from the Delaware River to downgradient pumped wells located just east of the model area in central Camden County. Simulation results show an important connection between the Intermediate sand and the Lower aquifer of the Potomac-Raritan-Magothy aquifer system in the vicinity of the chromium-contaminated area. The Delaware River contributes nearly 10 Mgal/d to the flow system, whereas recharge contributes about 6 Mgal/d. Ground-water withdrawals within the model area account for nearly 14 Mgal/d (mostly from the Lower aquifer of the Potomac-Raritan-Magothy aquifer system).

Strategies to reduce mass and photons transfer limitations in heterogeneous photocatalytic processes: Hexavalent chromium reduction studies.

PubMed

Marinho, Belisa A; Cristóvão, Raquel O; Djellabi, Ridha; Caseiro, Ana; Miranda, Sandra M; Loureiro, José M; Boaventura, Rui A R; Dias, Madalena M; Lopes, José Carlos B; Vilar, Vítor J P

2018-07-01

The current work presents different approaches to overcome mass and photon transfer limitations in heterogeneous photocatalytic processes applied to the reduction of hexavalent chromium to its trivalent form in the presence of a sacrificial agent. Two reactor designs were tested, a monolithic tubular photoreactor (MTP) and a micro-meso-structured photoreactor (NETmix), both presenting a high catalyst surface area per reaction liquid volume. In order to reduce photon transfer limitations, the tubular photoreactor was packed with transparent cellulose acetate monolithic structures (CAM) coated with the catalyst by a dip-coating method. For the NETmix reactor, a thin film of photocatalyst was uniformly deposited on the front glass slab (GS) or on the network of channels and chambers imprinted in the back stainless steel slab (SSS) using a spray system. The reaction rate for the NETmix photoreactor was evaluated for two illumination sources, solar light or UVA-LEDs, using the NETmix with the front glass slab or/and back stainless steel slab coated with TiO 2 -P25. The reusability of the photocatalytic films on the NETmix walls was also evaluated for three consecutive cycles using fresh Cr(VI) solutions. The catalyst reactivity in combination with the NETmix-SSS photoreactor is almost 70 times superior to one obtained with the MTP. Copyright © 2018 Elsevier Ltd. All rights reserved.

Hydrogeochemical processes and impact of tanning industries on groundwater quality in Ambur, Vellore district, Tamil Nadu, India.

PubMed

Kanagaraj, G; Elango, L

2016-12-01

The present study was carried out to determine the hydrogeochemical processes and the impact of tanning industries on groundwater in Ambur, Vellore district, Tamil Nadu, India. Thirty groundwater samples were collected during pre monsoon (July 2015) and post monsoon (January 2016) from the open and shallow wells around this region and were analyzed for major ions and chromium. The major ion concentration follows the order of Na + > Ca 2+ > Mg 2+ > K + (cations) and Cl - > HCO 3 - > SO 4 2- > NO 3 - (anions) for both seasons. The high concentrations of Na + , Cl - , and Cr around the tannery regions indicate the impact of effluent discharged from tannery units. In general, the groundwater of this study area is of Na + -Cl - type, which is due to the mixing of tannery effluent and cation exchange process. Ionic ratio indicates that the silicate weathering influences the groundwater chemistry. The permissible limit of chromium in the groundwater exceeds in over 50 % of the sampling wells. The factor analysis reveals that the dominant source for ionic contents is due to tannery effluents and cation exchange processes. To overcome this situation, it is essential to improve the performance of the effluent treatment plants so as to remove the salinity of wastewater and to plan for rainfall recharge structures for improving the groundwater recharge.

40 CFR 467.23 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2013 CFR

2013-07-01

...) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions... rolled with emulsions Chromium 0.057 0.024 Cyanide 0.038 0.016 Zinc 0.19 0.079 Aluminum 0.84 0.42 Subpart...

40 CFR 467.23 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2011 CFR

2011-07-01

...) EFFLUENT GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions Subcategory... rolled with emulsions Chromium 0.057 0.024 Cyanide 0.038 0.016 Zinc 0.19 0.079 Aluminum 0.84 0.42 Subpart...

40 CFR 467.23 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2012 CFR

2012-07-01

...) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions... rolled with emulsions Chromium 0.057 0.024 Cyanide 0.038 0.016 Zinc 0.19 0.079 Aluminum 0.84 0.42 Subpart...

40 CFR 467.23 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2014 CFR

2014-07-01

...) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ALUMINUM FORMING POINT SOURCE CATEGORY Rolling With Emulsions... rolled with emulsions Chromium 0.057 0.024 Cyanide 0.038 0.016 Zinc 0.19 0.079 Aluminum 0.84 0.42 Subpart...

40 CFR 433.14 - Effluent limitations representing the degree of effluent reduction attainable by applying the...

Code of Federal Regulations, 2010 CFR

2010-07-01

... average shall not exceed Milligrams per liter (mg/l) Cadmium (T) 0.69 0.26 Chromium (T) 2.77 1.71 Copper... agreement between a source subject to those limits and the pollution control authority, the following...

40 CFR 433.15 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2011 CFR

2011-07-01

... per liter (mg/l) Cadmium (T) 0.69 0.26 Chromium (T) 2.77 1.71 Copper (T) 3.38 2.07 Lead (T) 0.69 0.43... those limits and the pollution control authority. The following amenable cyanide limit may apply in...

40 CFR 433.14 - Effluent limitations representing the degree of effluent reduction attainable by applying the...

Code of Federal Regulations, 2011 CFR

2011-07-01

... average shall not exceed Milligrams per liter (mg/l) Cadmium (T) 0.69 0.26 Chromium (T) 2.77 1.71 Copper... agreement between a source subject to those limits and the pollution control authority, the following...

40 CFR 433.15 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2010 CFR

2010-07-01

... per liter (mg/l) Cadmium (T) 0.69 0.26 Chromium (T) 2.77 1.71 Copper (T) 3.38 2.07 Lead (T) 0.69 0.43... those limits and the pollution control authority. The following amenable cyanide limit may apply in...

40 CFR 471.35 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... Fluoride 13.9 6.15 (w) Molten salt rinse. Subpart C—PSNS Pollutant or pollutant property Maximum for any 1... with molten salt Chromium 0.312 0.127 Nickel 0.464 0.312 Fluoride 50.2 22.3 (x) Ammonia rinse. Subpart...

40 CFR 471.35 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... Fluoride 13.9 6.15 (w) Molten salt rinse. Subpart C—PSNS Pollutant or pollutant property Maximum for any 1... with molten salt Chromium 0.312 0.127 Nickel 0.464 0.312 Fluoride 50.2 22.3 (x) Ammonia rinse. Subpart...

40 CFR 471.33 - New source performance standards (NSPS).

Code of Federal Regulations, 2013 CFR

2013-07-01

... the range of 7.5 to 10.0 at all times. (w) Molten salt rinse. Subpart C—NSPS Pollutant or pollutant... nickel-cobalt treated with molten salt Chromium 0.312 0.127 Nickel 0.464 0.312 Fluoride 50.2 22.3 Oil and...

40 CFR 471.34 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2012 CFR

2012-07-01

... 0.035 Nickel 0.128 0.086 Fluoride 13.9 6.15 (w) Molten salt rinse. Subpart C—PSES Pollutant or...-pounds) of nickel-cobalt treated with molten salt Chromium 0.312 0.127 Nickel 0.464 0.312 Fluoride 50.2...

40 CFR 471.33 - New source performance standards (NSPS).

Code of Federal Regulations, 2012 CFR

2012-07-01

... the range of 7.5 to 10.0 at all times. (w) Molten salt rinse. Subpart C—NSPS Pollutant or pollutant... nickel-cobalt treated with molten salt Chromium 0.312 0.127 Nickel 0.464 0.312 Fluoride 50.2 22.3 Oil and...

40 CFR 471.34 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2013 CFR

2013-07-01

... 0.035 Nickel 0.128 0.086 Fluoride 13.9 6.15 (w) Molten salt rinse. Subpart C—PSES Pollutant or...-pounds) of nickel-cobalt treated with molten salt Chromium 0.312 0.127 Nickel 0.464 0.312 Fluoride 50.2...

40 CFR 471.34 - Pretreatment standards for existing sources (PSES).

Code of Federal Regulations, 2014 CFR

2014-07-01

... 0.035 Nickel 0.128 0.086 Fluoride 13.9 6.15 (w) Molten salt rinse. Subpart C—PSES Pollutant or...-pounds) of nickel-cobalt treated with molten salt Chromium 0.312 0.127 Nickel 0.464 0.312 Fluoride 50.2...

40 CFR 471.33 - New source performance standards (NSPS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... the range of 7.5 to 10.0 at all times. (w) Molten salt rinse. Subpart C—NSPS Pollutant or pollutant... nickel-cobalt treated with molten salt Chromium 0.312 0.127 Nickel 0.464 0.312 Fluoride 50.2 22.3 Oil and...

40 CFR 471.35 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2014 CFR

2014-07-01

... Fluoride 13.9 6.15 (w) Molten salt rinse. Subpart C—PSNS Pollutant or pollutant property Maximum for any 1... with molten salt Chromium 0.312 0.127 Nickel 0.464 0.312 Fluoride 50.2 22.3 (x) Ammonia rinse. Subpart...

An integrated geochemical, geophysical and mineralogical study of river sediments in alpine area and soil samples near steel plant, in Austria

NASA Astrophysics Data System (ADS)

Irfan, M. I.; Meisel, T.

2012-04-01

Concentration of nickel and chromium in any part of the ecosystem is important for environmental concerns in particular human health due to the reason that some species of them can cause health problem e.g. dermatitis and cancer. Sediment samples collected form a river Vordernberger Bach (Leoben, Austria) in an alpine region and soil samples collected in an area adjacent to steel production unit in same narrow valley were investigated. In previous studies a correlation between magnetic susceptibility values and concentration of nickel and chromium showed that a magnetic susceptibility meter can be used to point out the contaminated areas as in-situ device. The purpose of the whole study is to understand the real (point or diffuse, anthropogenic or geogenic) sources of contamination of soils, water and river sediments through heavy metal deposition. Unseparated, magnetic and non-magnetic fractions of soil samples were investigated for geochemical and mineralogical aspects with XRF, ICP-MS, EMPA, Multi-Functional Kappabridge (MFK1) and laser ablation coupled with ICP-MS. Mineralogical study of sediment samples for several sampling points with higher Ni and Cr content was performed. Sediment samples were sieved below 1.4 mm and then a concentrate of heavy minerals was prepared in the field through panning. Concentrated heavy minerals were then subjected for heavy liquid separation in the laboratory. Separated magnetic and non-magnetic fractions below 0.71/0.1 mm and density greater than 2.9 g/cm3 were selected for mineralogical investigation. The abundance of typical anthropogenic particles, e.g., spherical, tinder, roasted ores, iron and steel mill slag was observed under the microscope. Magnetite (mostly anthropogenic), maghemite, chromspinel, chromite (type I & II), (Ca,Al)-ferrite, wustite, apatite (anthropogenic), olivine mixed crystals, calcium silicate and spinel (anthropogenic) are found in magnetic fraction. Non-magnetic fractions contain hematite, siderite, ankerite, corundum (anthropogenic), garnet, chlorite, titanium oxide minerals (ilmenite, rutile, titanite) and amphibole etc. The observed significant increase in heavy metal content from the source region of the Vordernberger Bach at 1500 m above sea level to the confluence of the Vordernberger Bach with the Mur River at 540 m AMSL can be attributed to anthropogenic influence. As expected, the anthropogenic input is more pronounced in the vicinity of historic and current iron and steel production.

Human exposure risk to heavy metals through groundwater used for drinking in an intensively irrigated river delta

NASA Astrophysics Data System (ADS)

Vetrimurugan, E.; Brindha, K.; Elango, L.; Ndwandwe, Osman Muzi

2017-10-01

Drinking water containing heavy metals above the maximum permissible limits cause potential risk to human health. The aim of this study was to determine the groundwater suitability for drinking use based on heavy metal concentration and the associated human exposure risk in an intensively irrigated part of the Cauvery river basin, Tamil Nadu, India. Sixteen heavy metals analysed were in the order of dominance of chromium < zinc < copper < cadmium < cobalt < iron < aluminium < nickel < titanium < zirconium < boron < silver < manganese < lead < lithium < silicon in groundwater. Chromium and zinc were within permissible limits of the Bureau of Indian Standards for drinking water quality, and silver, lead and nickel were above limits in all the groundwater samples. In less than 50 % of the groundwater samples, aluminium, boron, cadmium, copper, iron and manganese exceeded their individual permissible limits. Heavy metal pollution index based on 11 heavy metals indicated that groundwater quality of this area is poor-to-unsuitable. Non-carcinogenic risk for humans due to ingestion of groundwater through drinking water pathway was very high for infants, children and adults. Silver, lead, nickel, cadmium and manganese largely contributed to the health hazard. Sources of heavy metals were identified to be geological and from human activities, i.e., application of fertilizers in agricultural fields, seawater intrusion due to intensive pumping for agriculture and wastewater from industries. Groundwater and surface water in this area pose large threat due to high levels of heavy metals, and it is necessary to avoid this water for drinking due to potential risk of health hazard. This study also demonstrated the application of HPI and human exposure hazard index to study the groundwater quality based on heavy metals' concentration.

Effects of chromium malate on glycometabolism, glycometabolism-related enzyme levels and lipid metabolism in type 2 diabetic rats: A dose–response and curative effects study

PubMed Central

Feng, Weiwei; Mao, Guanghua; Li, Qian; Wang, Wei; Chen, Yao; Zhao, Ting; Li, Fang; Zou, Ye; Wu, Huiyu; Yang, Liuqing; Wu, Xiangyang

2015-01-01

Aims/Introduction The present study was designed to evaluate the effect of chromium malate on glycometabolism, glycometabolism-related enzyme levels and lipid metabolism in type 2 diabetic rats, and dose–response and curative effects. Materials and Methods The model of type 2 diabetes rats was developed, and daily treatment with chromium malate was given for 4 weeks. A rat enzyme-linked immunosorbent assay kit was used to assay glycometabolism, glycometabolism-related enzyme levels and lipid metabolism changes. Results The results showed that the antihyperglycemic activity increased with administration of chromium malate in a dose–dependent manner. The serum insulin level, insulin resistance index and C-peptide level of the chromium malate groups at a dose of 17.5, 20.0 and 20.8 μg chromium/kg bodyweight were significantly lower than that of the model, chromium trichloride and chromium picolinate groups. The hepatic glycogen, glucose-6-phosphate dehydrogenase and glucokinase levels of the chromium malate groups at a dose of 17.5, 20.0 and 20.8 μg chromium/kg bodyweight were significantly higher than that of the model, chromium trichloride and chromium picolinate groups. Chromium malate at a dose of 20.0 and 20.8 μg chromium/kg bodyweight significantly changed the total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and triglycerides levels compared with the chromium trichloride and chromium picolinate groups. Conclusions The results showed that chromium malate exhibits greater benefits in treating type 2 diabetes, and the curative effect of chromium malate is superior to chromium trichloride and chromium picolinate. PMID:26221518

Evaluation of aquatic toxicities of chromium and chromium-containing effluents in reference to chromium electroplating industries.

PubMed

Baral, A; Engelken, R; Stephens, W; Farris, J; Hannigan, R

2006-05-01

This study evaluated aquatic toxicities of chromium and chromium-containing laboratory samples representative of effluents from chromium electroplating industries, and compared the aquatic environmental risks of hexavalent and trivalent chromium electroplating operations. Trivalent chromium electroplating has emerged as an acceptable alternative to hazardous hexavalent chromium electroplating. This process substitution has reduced the human health impact in the workplace and minimized the production of hazardous sludge regulated under the Resource Conservation and Recovery Act (RCRA). The thrust behind this research was to investigate whether trivalent chromium electroplating operations have lower adverse impacts on standardized toxicity test organisms. Ceriodaphnia dubia and Pimephales promelas were used to investigate toxicities of trivalent chromium (Cr (III)), hexavalent chromium (Cr (VI)), and industrial effluents. In agreement with previous studies, Cr (III) was found to be less toxic than Cr (VI). Despite having several organic and inorganic constituents in the effluents obtained from trivalent chromium plating baths, they exhibited less adverse effects to C. dubia than effluents obtained from hexavalent chromium electroplating baths. Thus, transition from hexavalent to trivalent chromium electroplating processes may be justified. However, because of the presence of organic constituents such as formate, oxalate, and triethylene glycol in effluents, trivalent chromium electroplating operations may face additional regulatory requirements for removal of total organic carbon.

Genetic Predisposition for Dermal Problems in Hexavalent Chromium Exposed Population

PubMed Central

Sharma, Priti; Bihari, Vipin; Agarwal, Sudhir K.; Goel, Sudhir K.

2012-01-01

We studied the effect of genetic susceptibility on hexavalent chromium induced dermal adversities. The health status of population was examined from the areas of Kanpur (India) having the elevated hexavalent chromium levels in groundwater. Blood samples were collected for DNA isolation to conduct polymorphic determination of genes, namely: NQO1 (C609T), hOGG1 (C1245G), GSTT1, and GSTM1 (deletion). Symptomatic exposed subjects (n = 38) were compared with asymptomatic exposed subjects (n = 108) along with asymptomatic controls (n = 148) from a non contaminated reference community. Exposed symptomatic group consisted of 36.8% subjects who were GSTM1 null genotyped as compared to asymptomatic where only 19.4% subjects were null. The exposed subjects with GSTM1 null genotype were more susceptible to dermal adversities in comparison with wild genotyped subjects (OR = 2.42; 95% CI = 1.071–5.451). Age, smoking, gender or duration of residence were not found to have any confounding effect towards this association. Association with other genes was not statistically significant, nonetheless, possible contribution by these genes cannot be ruled out. In conclusion, variation in the polymorphic status of GSTM1 gene may influence dermal outcomes among residents from Cr(VI) contaminated areas. Further studies are therefore, needed to examine these observations among different population groups. PMID:22919465

IN-SITU CR(VI) SOURCE AND PLUME TREATMENT USING A FERROUS IRON BASED REDUCTANT

EPA Science Inventory

A large volume of chromite ore processing residue (COPR) generated from ferrochrome production operations is present at the Macalloy Corporation Superfund site in Charleston, S.C. Groundwater hexavalent chromium (Cr(VI)) concentrations in the approximately 20 acre-foot COPR satu...

40 CFR 467.63 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2011 CFR

2011-07-01

...) EFFLUENT GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Emulsions or Soaps... emulsions or soaps Chromium 0.205 0.084 Cyanide 0.135 0.056 Zinc 0.681 0.285 Aluminum 3.00 1.49 Subpart F...

40 CFR 433.17 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2011 CFR

2011-07-01

... (mg/l) Cadmium (T) 0.11 0.07 Chromium (T) 2.77 1.71 Copper (T) 3.38 2.07 Lead (T) 0.69 0.43 Nickel (T... limits and the pollution control authority, the following amenable cyanide limit may apply in place of...

40 CFR 433.17 - Pretreatment standards for new sources (PSNS).

Code of Federal Regulations, 2010 CFR

2010-07-01

... (mg/l) Cadmium (T) 0.11 0.07 Chromium (T) 2.77 1.71 Copper (T) 3.38 2.07 Lead (T) 0.69 0.43 Nickel (T... limits and the pollution control authority, the following amenable cyanide limit may apply in place of...

40 CFR 467.52 - Effluent limitations representing the degree of effluent reduction attainable by the application...

Code of Federal Regulations, 2010 CFR

2010-07-01

... (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS ALUMINUM FORMING POINT SOURCE CATEGORY Drawing With Neat Oils... drawn with neat oils Chromium 0.022 0.0090 Cyanide 0.015 0.0050 Zinc 0.073 0.031 Aluminum 0.32 0.160 Oil...

40 CFR 437.21 - Effluent limitations attainable by the application of the best practicable control technology...

Code of Federal Regulations, 2011 CFR

2011-07-01

... CENTRALIZED WASTE TREATMENT POINT SOURCE CATEGORY Oils Treatment and Recovery § 437.21 Effluent limitations....6 Metal Parameters Arsenic 2.95 1.33 Cadmium 0.0172 0.0102 Chromium 0.746 0.323 Cobalt 56.4 18.8...