825results about "Testing organic contamination in water" patented technology

A water quality detection system for distributed water supply network. The system, 1, comprises a multiplicity of detectors, 5, wherein each detector of the detectors is capable of monitoring at least one attribute of water and providing a signal related to the attribute. A controller, 7, is provided which is capable of receiving each signal and comparing the signal to a control signal for the attribute. A response mechanism, 9, is responsive to the controller and activated when at least one signal matches the control signal. An access gate, 10, limits access to at least one of the detector, the controller or the response mechanism. An access key, 13, is provided for comparing a user attribute with a stored attribute wherein when the user attribute matches the stored attribute access is provided into the access gate.

In some embodiments, the present invention generally relates to the separation of blood within a device to form plasma or serum. In some embodiments, the present invention generally relates to the removal of fluids, such as blood, contained within a device. For example, a device may be applied to the skin of a subject to receive blood from the subject and pass the blood through a separation membrane, which separates the blood into plasma and a portion concentrated in blood cells. As another example, blood or plasma may be allowed to clot within the device and serum (the unclotted portion of the blood) may be withdrawn from the device. The device may contain, in some cases, a vacuum source such as a pre-packaged vacuum to facilitate receiving of blood and/or passage of the blood through the separation membrane to produce plasma or serum.

The present invention generally relates to systems and methods for receiving blood (or other bodily fluids) from a subject, e.g., from or beneath the skin of a subject. In some cases, the blood (or other bodily fluids) may be deposited on a membrane or other substrate. For example, blood may be absorbed in a substrate, and dried in some cases to produce a dried blood spot. In one aspect, the present invention is generally directed to devices and methods for receiving blood from a subject, e.g., from the skin, using devices including a substance transfer component (which may contain, for example, one or more microneedles), and directing the blood on a substrate, e.g., for absorbing blood. The substrate, in some embodiments, may comprise filter paper or cotton-based paper. After absorption of some blood onto the substrate, the substrate may be removed from the device and shipped or analyzed.

An access casing assembly structured for placement at least partially within a subterranean formation by forcing the access casing assembly thereinto, comprising a plurality of casing sections operably coupled to form a central elongated cavity for providing access to the subterranean region is disclosed. Further, a tip portion of the access casing assembly may include a porous filter through which liquid or gas may communicate with the central elongated cavity. Also, a receiving member or at least one engagement hub may form a portion of the central elongated cavity and may include an engagement feature configured for selectively and lockingly engaging a locking structure of a device to be positioned within the access casing assembly. Methods of use are disclosed. A tensiometer is disclosed including a chamber structured for allowing at least partially filling with a fluid subsequent to contact therewith.

Methods for analyzing aromatic hydrocarbons dissolved in water are discussed. The methods include providing a substrate coated with a thin film layer of a material, wherein the material has a high affinity for at least one aromatic hydrocarbon, the material is substantially optically transparent, and the material has near-zero auto fluorescence, inserting the coated substrate directly into an environmental location including water, waiting for an exposure time permitting at least one aromatic hydrocarbon to absorb into the thin film layer, retrieving the coated substrate from the environmental location, removing any non-absorbed matter from the coated substrate, and performing fluorescence analysis on the coated substrate to detect aromatic hydrocarbons present in the thin film layer. Also methods for analyzing aromatic hydrocarbons dissolved in water contained in coated vessels are provided.

A colorimetric reagent in the form of nanoparticles, composite nanoparticles, and nanoparticle coatings, including methods of use, methods of preparation, deposition, and assembly of related devices and specific applications. The colorimetric reagent comprises cerium oxide nanoparticles which are used in solution or immobilized on a solid support, either alone or in conjunction with oxidase enzymes, to form an active colorimetric component that reacts with an analyte to form a colored complex. The rate of color change and the intensity of the color are proportional to the amount of analyte present in the sample. Also described is the use of ceria and doped ceria nanoparticles as an oxygen storage/delivery vehicle for oxidase enzymes and applications in biocatalytic processes in anaerobic conditions of interest in biomedicine and bioanalysis. Further described are a variety of related applications of the disclosed technology including clinical diagnosis, in vivo implantable devices, food safety, and fermentation control.

The use of an isomer of anthracene disulfonic acid as an inert fluorescent tracer is described and claimed. The utility of this type of inert fluorescent tracer in boiler systems to trace unwanted carryover of boiler water into a steam line is also described and claimed.

The present invention relates to an oil spill identification system and oil spill identification sensors to be used in connection with this system. The system is used primarily on fixed offshore structures, but may also be used on fixed onshore constructions. The sensor comprises a combination of a radar and at least a microwave radiometer. The data collected are transmitted to a control station. Preferably, the transmittal takes place at pixel level between the sensors and the control station. The control station processes the data received at pixel level and transmits data to an end-user, preferably through the internet. The invention also relates to a method for utilizing the system and a use of the system.

A sensor system detects organophosphorus pesticide residue by inducing the aggregation of gold nanoparticles. A method comprises aggregating gold nanoparticles by a reaction between an organophosphorus pesticide and imidazole or a green fluorescent protein (GFP), and detecting the organophosphorus pesticide based on a absorption spectral change resulting from the aggregation. The system for detecting pesticide residue is useful as a biosensor for analyzing pesticide residue in situ, because the optical change of the reagent by the presence of an organophosphorus pesticide is distinct, the detection speed is fast, and the range of detection limits is broad.

The invention provides compositions useful as molecular probes. In particular, the invention provides activatable cell penetrating peptides comprising a fluorescence donor and a fluorescence acceptor. Exemplary fluorescence donors and fluorescence acceptors include compounds derived from cyanine. Also provided are ratiometric, multispectral, and excitation lifetime imaging methods for detecting the molecular probes provided herein.

The invention describes a method for determining aggregation in protein, peptide or peptoid formulation, without the use of probes or additives. The method uses FTIR spectroscopy combined with the two-dimensional correlation analysis (2DCOS) which allows for the determination of the presence of aggregates, the determination of the mechanism of aggregation, allowing for correction in the pipeline manufacturing process of the protein to once again generate viable protein. In addition, the thermal transition of the protein can also be determined and a 2DCOS plot generated to compare with the established viable protein, allowing for quality control, stability and viability of the desired protein product. The ease of sample preparation and data analysis allows for the automation of this method.

The invention discloses a multi-channel photobacteria on-line water quality toxicity monitoring device and a monitoring method thereof. The device comprises a diaphragm water pump, wherein a water inlet of the diaphragm water pump is connected with a membrane filter through a water pipe and then is connected with a water sample pool; a water outlet of the diaphragm water pump is connected with an overflow type branch sampler through a water pipe; a plurality of water sample monitoring modules form a plurality of monitoring channels which are connected to the overflow type branch sampler; waste liquid outlets of the plurality of the water sample monitoring modules are parallelly connected with an external peristaltic pump; and an outlet of the peristaltic pump is connected to a waste liquid tank. The monitoring method comprises the following steps: a water sample is sucked into the membrane filter consisting of a hollow fibrous membrane by the diaphragm pump, suspensions and bacteria in water are filtered, and the water sample enters the overflow type branch sampler. Then the bioluminescent intensity of photobacteria is detected in a real-time mode through a toxicity detection module. After a detection experiment is finished, the external peristaltic pump discharges a waste liquid in a reactor into the waste liquid tank; and the device can realize the on-line detection of biologic toxicity of the water from water sources, municipal sewage, and input water of water works, and has the characteristics of simple operation, convenient maintenance, high automation degree, and so on.

The disclosure relates to a tracking device configured to track an object in space, such as the sun, as the object moves across the sky. The tracking device may further be configured to direct a payload toward the object or toward an angle relative to the object. The tracking device may continuously or intermittently determine the location of the moving object, and adjust the position of the payload accordingly. The tracking device may calculate the position of the moving object based on GPS information, such as triangulated coordinates of the tracking device, date, and time. Generally, the tracking device may be capable of tracking an object such as the sun from anywhere on the earth's surface. The tracking device may employ one or more actuation assemblies to position the payload toward or relative to the moving object. The one or more actuation assemblies may operate through linear motion.

Total organic carbon in an aqueous or gaseous sample is measured by admitting the sample and an oxidant gas to a cell transparent to plasma, establishing a relatively low energy plasma in the cell, and measuring the CO.sub.2 thus produced using FTIR, NDIR, or conductivity-based techniques.

Methods and apparatus are disclosed for determination of the total concentration of organic carbon compounds in aqueous process streams utilizing a pulsed-flow technique for irradiating a water sample in a chamber (3) with UV or similar wavelength radiation.

The invention discloses an underground water online monitoring and representative water sample collection integral self-control device and a control method thereof and relates to the technical field of underground water monitoring and water sample collection. The device comprises a control operation station, a representative water sample judgment collection system and an online in-situ monitoringsystem, wherein the control operation station is arranged on the ground; the online in-situ monitoring system is connected with the control operation station and is arranged under an underground waterlevel in a well; the online in-situ monitoring system is connected with a water pump under the underground water level through a tube; the water pump is connected with a stagnant water collector anda water sample collector through tubes; an online spectrum water quality monitor II and a common parameter water quality analyzer II of the online in-situ monitoring system are used for monitoring andanalyzing water inside the stagnant water collector and the water sample collector. To ensure that fresh water samples of water layers are monitored, and water samples are collected in multiple dimensions from multiple sites to stably judge water sample representativeness according to water quality parameters. Integration of monitoring and sampling techniques is deepened, and in-situ informationacquisition uncertainty is greatly reduced.

Described herein is an underwater vehicle having a vehicle body with a buoyancy controller adapted to vary the buoyancy of the vehicle in order to control motion of the vehicle through an underwater environment. The vehicle further includes a sampling system and a sensor arrangement. The sampling system is adapted to sequentially sample fluid from the underwater environment at specified sampling times resulting in a sample sequence, each sample associated with a sample time and a fluid flow rate. The sensor arrangement includes a plurality of molecule sensors adapted to sense organic molecules in each respective sample of the sample sequence.

A chromogenic oxazine compound for the colorimetric detection of cyanide was designed. Indeed, the [1,3]oxazine ring of our compound opens to form a phenolate chromophore in response to cyanide. The heterocyclic com-pound may be comprised of fused benzooxazine and indoline rings:

wherein R¹ is an alkyl (e.g., methyl, ethyl, propyl, isopropyl, butyl, isobutyl), a substituted alkyl, a cycloalkyl (e.g., cyclopentyl, cyclohexyl), a substituted cycloalkyl, an aryl (e.g., phenyl), or a substituted aryl and R² is a chromophore (e.g., nitroso, nitro, azo dyes). This quantitative chromogenic transformation permits the detection of micromolar concentrations of cyanide in water. Furthermore, our chromogenic oxazine is insensitive to the presence of large concentrations of fluoride, chloride, bromide or iodide anions, which are generally the principal interferents in the colorimetric detection of cyanide.

The invention disclosed is a total organic carbon (TOC) analyzer comprised of an electrochemical cell comprising a diamond-film electrode (2) doped with boron or other conductivity including material. The diamond-film electrode is the working electrode and carries out the oxidation of TOC to produce carbon dioxide. The apparatus further comprises sensors for detecting the carbon dioxide produced. Such sensors include but are not limited to a tunable diode laser (1) and/or ion-selective electrode (5). The invention also discloses a method for measuring TOC in an aqueous solution using a total organic carbon analyzer.

A method and apparatus for deriving a refinery product property value based on data produced from a globally-calibrated spectrographic analyzer and data from a non-spectrographic analyzer.