We have established a highly technical, state-of-the-art laboratory facility in College Station, Texas, and now direct an accomplished, motivated, and competent staff with a broad range of published expertise in geochemical and environmental chemistry as well as in biological, geological and physical oceanography.
From determining trace contaminants in sediment, soils, tissue, and water to oil spill response, we have extensive experience with programs such as NOAA’s Status and Trends Mussel Watch (1999-currently), United States Fish and Wildlife Analytical Control Facility (2002-currently), and our involvement in oil spill response as with Mississippi Canyon 252 (Deepwater Horizon) Natural Resource Damage Assessment (2010-currently).
We have participated in National Institute of Standards and Technology (NIST) laboratory intercalibrations for tissue, sediments and crude oil from 1998 through 2011.
B&B Laboratories is an affiliate of TDI-Brooks International which are both owned and operated by world-renowned geochemists Dr. Jim Brooks and Dr. Bernie Bernard in College Station, Texas. B&B Labs provides high-quality analytical services and scientific interpretation with a focus on petroleum geochemistry, surface geochemical exploration, oil spill response, environmental chemistry, and environmental assessments via our laboratory affiliate, B&B Laboratories.
Our company has over 20 years of experience and has been the choice laboratory for programs such as NOAA’s Status and Trends Mussel Watch (1999-currently), United States Fish and Wildlife Analytical Control Facility (2002-currently), oil spill response as with Mississippi Canyon 252 (Deepwater Horizon) Natural Resource Damage Assessment (2010-currently). Our company has been ISO 9001 accredited since 2011 and is currently in the process of obtaining ISO 17025:2017 accreditation.
We take great pride in providing the highest quality trace-level organic chemical analyses for industries that require monitoring of analytes outside the scope and detection limits of typical regulatory methods. Our methods are based on highly modified EPA methods that are performance-based and meet the requirements of ISO 17025:2017. We specialize in the extraction and analysis of organic compounds in soils, sediment, and non-human tissue (i.e. fish, bivalves, bird eggs, blubber). Experienced scientists review the data to ensure that they are scientifically sound and fulfill our customer’s requirements and requests.
Our Analytical Repertoire includes the following:
Polycyclic Aromatic Hydrocarbons
As part of our hydrocarbon forensics, we routinely determine an extensive list of parent PAH and alkyl-substituted homologs in sediment, water, and tissue. PAH analysis is performed using gas chromatography / mass spectrometry (GC/MS) in selected ion monitoring (SIM) mode. Method detection limits for PAHs using this method are extremely low (< 0.5 ng/dry g for sediment, < 10 ng/L for water, and < 10 ng/wet g for tissue).
TPH Determination (n-C10 –n-C40) In conjunction with our PAH determination, we offer the analysis of Saturate Hydrocarbons with n-alkanes ranging from n-C10 through n-C40 as well as several Isoprenoids in identifying petroleum contamination in environmental samples and/or characterization of petroleum products. Also available is the analysis of samples for Total Petroleum Hydrocarbon (TPH). Aliphatic Hydrocarbon (ALI) determination is a quantitative technique used for the analysis of normal alkanes with 10 to 40 carbons (C10 to C40), and the isoprenoids pristane and phytane, in extracts of sediment and water. This technique is very sensitive for “fingerprinting” petroleum and for following its degradation in the environment. Quantitation is performed by high-resolution capillary gas chromatography with flame ionization detection (GC/FID). Method detection limits for compounds determined using this method are very low (< 0.02 mg/dry g for sediment, and < 0.32 mg/L for water). Total Petroleum Hydrocarbon (TPH) determination refers to the quantitative determination of the sum of all hydrocarbons, degraded and non-degraded, that may be extracted from a sediment or water sample. The analysis is performed gravimetrically or by gas chromatography / flame ionization detection (GC/FID). The gravimetric technique is an inexpensive and quick screening tool for oil spill response projects. The gravimetric TPH method is performed by solvent extracting hydrocarbons from a sample, concentrating the extract by reducing the extract volume, and weighing a portion of the extract. The more expensive GC technique provides additional sensitivity and information. This method takes a portion of the concentrated extract (as above) and injects it into a GC/FID. The resulting chromatogram is integrated, using a straight line, between the retention time for the n-alkane n-C10 and the retention time for the n-alkane n-C40. This integration includes most extractable petroleum related hydrocarbons. Using this method, the Total Resolvable Hydrocarbons (TRH) and the Unresolved Complex Mixture (UCM) may also be determined. The TRH are non-degraded hydrocarbons which appear as peaks in the chromatogram. The UCM is the area under the chromatogram (excluding the peaks) representing degraded hydrocarbons. As an oil degrades, the UCM hump becomes larger and the TRH decreases. TPH is the sum of TRH and UCM.
PCB & Chlorinated Pesticides Determination
As part of our long standing involvement with NOAA and USFWS, TDI-Brooks routinely analyze an extensive congener specific list of PCBs and Chlorinated Pesticides from Chlordanes, DDTs, and isomers of Hexachlorohexanes to name a few. High quality Chlorinated Pesticide and Polychlorinated biphenyl (PCB) dtermination is performed using high resolution gas chromatography / electron capture detection (GC/ECD) and is a quantitative analytical technique used for the determination of chlorinated hydrocarbons in extracts of tissue, water, and sediment. Method Detection Limits using this technique are very low (< 0.2 ng/dry g for sediment, <5 ng/L for water, and <4 ng/wet g for tissue).
Brominated Flame Retardants
As part of a new group of emerging contaminates , we also offer the determination of Polybrominated Diphenyl Ether (PBDE) & Polybrominated Biphenyls (PBB). Used as flame retardants, these compounds can be found in many commercial and household items from plastic toys, textiles, building materials and laptops. As a quantitative technique used for the determination of PBDE/PBBs (individual congeners) in extracts of sediment, water, and tissue, PBDE/PBB analysis is performed using gas chromatography / mass spectrometry Negative Chemical Ionization (GC/MS-NCI) and (GC/MS) in selected ion monitoring (SIM) mode at sub part per billion concentrations respectively.
% Carbon Determination
Employing the Lloyd Kahn procedure, we routinely analyze percent total carbon, percent organic carbon and percent inorganic carbon using the LECO corporation model 632 carbon analyzer in sediments and soils using direct combustion/infrared detection. In addition to the determination of solids for percent carbon, we can provide % carbon results for both fresh and marine water samples using the OI Analytical model 700 or 1010 Wet Oxidation Total Organic Carbon Analyzers.
We have a highly trained staff with a broad range of experience in environmental analytical techniques. If you require services not listed here, please contact us for more information
Not all laboratories can offer the services you require. We can facilitate extended services by partnering with other labs in order to provide you with a sole source solution to your analytical needs. Please contact us for more information..
Sample Receiving Hours: Monday – Friday: 7 am – 6 pm
New Year’s Day, Memorial Day, Independence Day, Thanksgiving Day, and Christmas Day.
Please contact us at 979-693-3446 to make arrangements for sample delivery outside of normal business hours.
Ms. Amanda Brewster, Sample Custodian (firstname.lastname@example.org)
Mr. Juan Ramirez, Laboratory Manager (email@example.com)
14391B S. Dowling Rd College Station, TX 77845
If you would like to learn more about our analytical services and capabilities, please contact:
Juan Ramirez, Environmental Laboratory Manager
firstname.lastname@example.org, + 979.777.0793
We take great pride in providing the highest quality trace-level geochemical analyses that go above and beyond the capabilities and scope of typical regulatory methods offered by other laboratories. Our methods are based on highly modified EPA methods that are performance-based and have been historically proven in numerous domestic and international programs over the past two decades. Our experienced geochemists review the data to ensure that they are scientifically sound and exceed our customer’s requirements and requests.
Our Geochemical Analytical Repertoire includes the following:
C15+ Hydrocarbon Determination
C15+ Hydrocarbon Determination refers to the determination of individual normal alkane hydrocarbons between 15 and 34 carbons. The determination also includes the isoprenoids pristane and phytane, and a determination of the unresolved complex mixture (UCM). The analytes are separated and detected by a flame ionization detector (GC/FID).
Core sections associated with recent seepage of petroleum may have a complete sequence of n-alkanes, plus the isoprenoids, pristane and phytane. Depending on the degree of biodegradation, a UCM hump may also be present. For severely biodegraded extracts, the n-alkanes and isoprenoids have been degraded and a large UCM hump is usually present.
Sites associated with recent, terrigenous organic matter typically have a low UCM value and an enrichment in long-chain (greater than n-C23) n-alkanes with odd-carbon predominance. The detection of a complete suite of n-alkanes plus pristane and phytane is especially strong evidence of the existence of migrated petroleum.
Interstitial Headspace Gas Determination
Interstitial Headspace Gas Determination refers to the determination of interstitial light hydrocarbon gases including methane, ethene, ethane, propene, propane, butenes, iso-butane, n-butane, neo-pentane, iso-pentane, and n-pentane (C1-C5) by Gas Chromatography/Flame Ionization Detection (GC/FID). The natural presence of high levels of C2+ alkane gases serves as a good indicator of migrating thermally-sourced gas, because ethane, propane, the butanes, and the pentanes are not microbially produced at high levels in marine sediments. The light hydrocarbon gases are not very soluble in water, so they can be extracted from a sediment and water sample into a gas such as nitrogen by a partitioning procedure. Sediment samples are canned immediately after piston core retrieval for headspace gas determinations. Sediment sections are immediately extruded from the core barrel’s liner into cans containing hydrocarbon-free 5 % Sodium Chloride solution. The cans are sealed after flushing the headspace with purified nitrogen, then frozen.
In the laboratory, the cans are thawed and kept at 40 deg C for at least 4 hours. The light hydrocarbons dissolved in the interstitial water are equilibrated with the nitrogen gas phase at that temperature by vigorous agitation with a high-speed shaker. Prior to the analysis of samples, a calibration curve is established for each analyte to determine the sensitivity and confirm the linear range of the GC/FID system. TDI-Brooks has developed a unique headspace gas can auto-sampler which allows for around-the-clock analysis with excellent accuracy and data reproducibility. Each autosampler batch analyzed includes samples, method blanks, and duplicates.
The computer software automatically integrates analyte peaks based on their retention times and analysts visually confirm that each analyte peak is integrated correctly by the software.
An automated extraction apparatus (Dionex ASE200 Accelerated Solvent Extractor) is used to extract various organic hydrocarbons from pre-dried sediment. The extractions are performed using hexane inside stainless-steel extraction cells held at elevated temperature and solvent pressure. This method of extraction minimizes the use of solvent and decreases the extraction time when compared to conventional Soxhlet extractions. The extracts dissolved in the hot solvent are transferred from the heated extraction cells to glass collection vials. Pre-cleaned, activated copper is added to each collection vial in order to minimize matrix interference.
Extracts are concentrated to a final volume of 8-ml using an evaporative solvent reduction apparatus (Zymark TurboVap II). Final extracts are submitted for hydrocarbon analysis by Total Scanning Fluorescence (TSF) and Gas Chromatography Flame Ionization Detection (GC/FID). Equipment is demonstrated to be interference-free with the analysis of method blanks. Oil spikes (extractions of a known amount of diluted crude oil) are analyzed with every sample-set in order to demonstrate the reproducibility of the extraction procedure
Total Scanning Fluorescence
Total Scanning Fluorescence (TSF) is a semi-quantitative analytical technique that is selectively sensitive to aromatic compounds and, as such, is a valuable tool for detecting the presence of petroleum related hydrocarbons in sediment extracts. Increasing TSF intensity (expressed in arbitrary intensity units) generally corresponds to increasing aromatic hydrocarbon concentrations in sediment extracts.
Sediments containing upward-migrated oil contain a higher concentration of larger aromatic compounds (3 or more benzene rings) and fluoresce at longer wavelengths, whereas sediment extracts containing upward-migrated gas or condensate fluoresce at shorter wavelengths. TSF patterns are typically insensitive to bacterial alteration except in severely biodegraded samples.
The TSF parameter R1 gives an estimate of the ratio of three and four-ring aromatics to two-ring aromatics. For extracts with high TSF maximum intensity, R1 values greater than 2 typically indicate the presence of mature hydrocarbons.A three-dimensional spectrum is acquired using software written for Perkin-Elmer Model LS 50B Fluorometers. A sample extract is placed in the pre-calibrated fluorometer, and scanned over a specified range of excitation wavelengths while measuring the resulting fluorescence emission intensities over a specified range of emission wavelengths. The resulting data is used to evaluate the sample extract for the presence of petroleum related aromatic hydrocarbons.
Gas Isotope Analysis
As part of our ever expanding capabilities in analysis of Surface Prospecting Services, we now offer Isotopic Analysis of mud gas as part of our Geochemical capabilities. Using the Compact Science Systems IDmicro Stable Isotope Ratio Mass Spectrometer (IRMS) to differentiate between biogenic and thermogenic gases, we can reliably measure d13C for C1 – C5 hydrocarbons with the use of purge and trap enrichment for low concentration samples.
If you would like to learn more about our geochemical analytical services and capabilities, please contact:
Mike Gaskins, Geochemical Laboratory Manager
email@example.com, + 979.693.3446
TDI-Brooks International, Inc. offers a comprehensive suite of geotechnical analytical services for characterizing offshore geotechnical samples. All of our services are offered in the onshore laboratory. Some of the services are also offered in conjunction with our offshore geotechnical programs.
Our Geotechnical Repertoire includes the following:
Atterberg Limits (Plastic Limit, Liquid Limit, and Plasticity Index)
The Atterberg limits are a set of “limits of consistency” of fine-grained soils. In current engineering usage, they are comprised of the plastic limit and the liquid limit. Occasionally, the shrinkage limit is included with the plastic and liquid limits. In most TDI-Brooks projects, the plastic and liquid limits are sufficient for soil characterization. The liquid limit is the water content of a soil at the arbitrarily defined boundary between the semi-liquid and plastic states. The plastic limit is the water content of a soil at the boundary between the plastic and semi-solid states. The plasticity index is the range of water content over which a soil behaves plastically. Numerically, it is the difference between the liquid limit and the plastic limit. Reference ASTM D4318.
Calcium Carbonate Content
The carbonate content (calcite equivalent) of soil is determined by treating a dried soil specimen with hydrochloric acid in a reactor. Carbon dioxide gas is evolved during the reaction between the acid and carbonate fraction of the specimen. The resulting pressure generated in the closed reactor is proportional to the calcite equivalent of the specimen. This pressure is measured with a suitable pressure gauge that is pre-calibrated with reagent grade calcium carbonate. Reference ASTM D4373.
Core splitting is our process of cutting a core section down the long axis and separating the two halves. This exposes a vertical cross section of a core, allowing the examination of sediment layers and geologic features. Often, this allows identification of layers for age dating. This is available for fine-grained sediments with high and medium moisture contents. We do not currently offer services for splitting hard/rock samples. Split core usually receive High Resolution Photography.
Measurement of sediment electrical resistivity is used for the control of corrosion of buried structures. Electrical resistivity is used both for the estimation of expected corrosion rates and for the design of cathodic protection systems. Resistivity measurements indicate the relative ability of a medium to carry electrical currents. When a metallic structure is immersed in a conductive medium, the ability of the medium to carry current will influence the magnitude of galvanic currents and cathodic protection currents. A soil box with 4 electrodes is used in the lab to conduct this test. Reference ASTM G57.
Grain Size – Hydrometer
Sediment grain sizes smaller than particles 75 microns can be determined using a sedimentation process. This test is appropriate for marine silts and clays. The particles are initially suspended in solution and then allowed to deposit over time. As they deposit, the density of the solution decreases. The changes in solution density are measured using a hydrometer. The rate at which the particles settle out of suspension can be interpreted to provide grain size distribution, represented by a gradation curve. The gradation curve may also include sieve data generated from the same sample. Reference ASTM D422.
Grain Size – Sieve
Sediment grain sizes larger than 75 microns can be determined by sieving. A standard sieve set corresponds to specifications in ASTM D422, however, other sieve sizes can be used upon request. The mass of sediment retained on each sieve provides grain size distribution and is plotted on a gradation curve. The gradation curve may also include hydrometer data from the same sample. Reference ASTM D422.
High Resolution Photography
High resolution photography is mostly used in conjunction with Core Splitting. We photograph 10-cm length portions of a core section with a Nikon D90 and merge the photos to generate a single image. These images are typically used by the client for observing geologic characteristics and sedimentology. We can photograph other samples in a high resolution format, but Standard Resolution Photography is also available for documentation and description purposes.
Magnetic susceptibility is a measure of the magnetic behavior of a sediment sample. Magnetic susceptibility measurements provide important information about the composition and properties of materials. In many cases, magnetic susceptibility is done with a multi-sensor core logger. TDI-Brooks can offer this testing separately. Reference Bartington Instruments MS3 Operations Manual.
Miniature Vane Shear
Miniature vane shear testing is performed to determine shear strength in very soft to stiff saturated fine-grained clayey sediments. We use a set of 4 calibrated torsion spring sets combined with a motorized vane shear device to determine strength. Reference ASTM D4648.
Moisture content is a test to determine how much water is in a sediment sample. It is a ratio of the mass of water to the mass of solids, reported in a percent. Since it is a ratio of water to solids, it can, and often does, exceed 100% in marine samples. Reference ASTM D2216.
Multi-Sensor Core Logging (MSCL)
Multi-sensor core logging is a quantitative method to determine geotechnical properties such as bulk density, porosity, void ratios, and water content in sediment cores using a GEOTEK multi-sensor core logger (MSCL). The MSCL can handle core sections up to 1.5-m long and can sample at intervals of 1-mm or greater and is a non-destructive test.
Percent Sand Determination
Percent sand determination is similar to grain size testing using sieves except that the number of sieves is reduced. A No. 4 sieve is used to separate gravel from the sample. A No. 200 sieve allows all the clay and silt to pass, leaving only the sand fraction in the No. 200 sieve.
pH of Soils
This specific pH of soils test is for uses other than corrosion testing. The test determines the degree of acidity or alkalinity in soil materials suspended in water and a 0.01 M calcium chloride solution. Measurements in both liquids are necessary to fully define the soil’s pH. The measurement of the pH of soils suspended in either water or calcium chloride solution is made with a potentiometer using a pH sensitive electrode system. The potentiometer is calibrated with buffer solutions of known pH. Reference ASTM D4972.
The pocket penetrometer is used to find preliminary soil strength values and is used for classification of cohesive soils. It indicates consistency, shear strength, and approximate unconfined shear strength. The direct-reading scale is in tons per square foot or kilograms per square centimeter. This is typically used for stiffer soils. As a classification tool, it should not replace laboratory testing or field analysis, or be used to produce design data.
Qualitative Physical Description (Munsell Color Description, Soil Type, Foram Content, Water Content, Cohesion)
The qualitative physical description gives a wide array of descriptive information for classification of soils. Color is described with color codes from a Munsell color chart. Soil type is a grain size description characterized as clay, silt, sand, or gravel or a combination of those terms. Foram content, water content, and cohesion are all described relatively with terms such as low, moderate, or high.
Remolded Miniature Vane Shear
Remolded miniature vane shear testing is performed to determine shear strength in very soft to stiff saturated fine-grained clayey sediments. We use a set of 4 calibrated torsion spring sets combined with a motorized vane shear device to determine strength. The procedure is the same as Miniature Vane Shear except the sample is remolded first, breaking down any existing sediment structure. Reference ASTM D4648.
Miniture Vane Spring Calibration
Torsion springs are a critical part for operating miniature vane shear test apparatus. Typically, these springs are used as a set of 4 springs. At TDI-Brooks International, Inc., we offer high-quality calibration for individual torsion springs and complete torsion spring sets for miniature vane systems. By using a calibrated digital torquemeter, our method exceeds the accuracy required by the ASTM D4648 Standard.
Specific gravity is the ratio of the mass of unit volume of soil at a stated temperature to the mass of the same volume of gas-free distilled water at a stated temperature. The specific gravity of a soil is determined by placing a certain mass of dry soil into a calibrated pycnometer and then filling the pycnometer with de-aired, distilled water under vacuum. Knowing the mass of the soil and the mass of de-aired water, the specific gravity of the soil solids can be determined. Reference ASTM D854.
Standard Resolution Photography
Standard resolution photography is used to capture visual representation of sediment characteristics. This type of photography can be used in conjunction with Qualitative Physical Descriptions (link) to gain a more complete understanding of sediment characteristics. It can also be used to document unique occurrences that cannot be adequately communicated with a written description. Photographs of this type are usually taken of a horizontal cross section of a core section.
Thixotropy of soils describes when a remolded soil sample hardens over time while maintaining constant water content and constant volume. The gaining in strength is due to gradual reorientation of molecules and a regaining of the chemical equilibrium. This property is dependent on physical and chemical characteristics of the soil being tested and is performed over a 30-day period.
The torvane is used to find preliminary soil strength values and is used for classification of cohesive soils. This is typically used for softer soils and has adapters allowing it to accommodate a larger range of strengths. As a tool for preliminary testing, it should not replace a more precise strength measurement tool or be used to produce design data.
Unconsolidated-Undrained Triaxial (UU Triaxial)
UU Triaxial testing is performed to determine the shear strength of an undrained and unconsolidated cylindrical sediment sample. Specifically, the sample is placed under a confining pressure to simulate the condition of being confined by surrounding soil. The sample is then failed axially while measuring the force applied to the sample and the deformation. Measuring these two values allows us to construct a stress-strain plot of the failure. Reference ASTM D2850.
Unit Weight (Density)
Unit weight is a ratio of weight to volume. We can also report the density which the ratio of mass to volume. The difference between the two values is only the acceleration due to gravity so one can be determined from the other. We use 2 different methods depending on the grain size. Unit weight and density testing is dependent on the specific soil structure and moisture content at the time of testing. Reference ASTM D7263.
If you would like to learn more about our analytical services and capabilities, please contact:
Nick Clark, Geotechnical Laboratory Manager
firstname.lastname@example.org, + 512.923.7200