A method and system for detecting sulfur fires that comprises a remote infrared or microwave sensor to detect sulfur dioxide gas and provide an unsupervised remote daytime and nighttime sulfur fire-watch, hot spot detection, early sulfur fire prevention, sulfur fire detection, or sulfur fire control of unattended combustible sulfur blocks, sulfur stockpiles, sulfur plants, or equipment using remote sensing devices that includes detection, measurement and analysis of electromagnetic radiation to determine the presence of sulfur dioxide gas.

A method of gas sensing performed by a processor electrically coupled to a gas sensor includes obtaining, by the gas sensor, a first electrical signal indicating a response of the gas sensor to a concentration of a target gas at the gas sensor, generating one or more second electrical signals according to the first electrical signal, determining a first condition in which the concentration at the gas sensor is increasing using the first electrical signal and the one or more electrical second signals, determining a second condition occurring after the first condition in which the concentration at the gas sensor is substantially constant using the first electrical signal and the one or more second electrical signals, and calculating a concentration value of the target gas according to the first electrical signal and the one or more second electrical signals. The calculating is performed while the concentration is substantially constant.

A novel approach, based on hybrid nanostructure gas sensors, to correlate metrics related to specific medical conditions to a signature created by the sensor's response to the Volatile Organic Compounds (VOCs) contained in human breath.

A method for desulfurizing molten steel comprising taking a sample out from molten steel after tapping from a converter or during secondary refining and analyzing the sample rapidly with high accuracy by a method comprising a high frequency induction heating step wherein the sample is combusted and oxidized under the high frequency induction heating in an oxygen atmosphere having an oxygen purity of 99.5 vol % or more to convert S in the sample into SO.sub.2 and an analyzing step wherein SO.sub.2-containing gas produced in the high frequency induction heating step is analyzed through an ultraviolet fluorescence method to quantify S concentration of the sample.

A gas sensor configured to detect a target gas in a gaseous atmosphere, for example NO.sub.2 or O.sub.3 in air, comprises: a transparent substrate; a gas sensitive detection layer supported by the transparent substrate, the gas sensitive detection layer comprising i) a gas sensitive detection material having an electrical impedance which is sensitive to the target gas and ii) connections configured to allow for detection of electrical impedance of the gas sensitive detection material; and a light source, for example a LED, configured to provide light to the gas sensitive detection layer through the transparent substrate. The gas sensor may operate at room temperature whilst requiring little power.

The invention of the present application relates to a system for accurately measuring fine-dust precursors. Among apparatuses that measure concentrations of NO.sub.x and SO.sub.x which are precursors of fine dust by use of tunable diode laser absorption spectroscopy (TDLAS), an apparatus that can control a temperature of a measurement cell equipped with prism-type multi-passes by using thermoelectric elements without vibration is provided.

A method of gas sensing includes obtaining a first signal by a gas sensor, generating one or more second signals according to the first signal, and calculating a first weight value corresponding to the first signal. The first signal indicates a response of the gas sensor to a concentration of a target gas at the gas sensor. The method of gas sensing further includes calculating one or more second weight values corresponding to each of the one or more second signals and calculating an estimated concentration of the target gas at the gas sensor according to the first weight value and the one or more second weight values.

A species-specific gas sensor and monitor comprising a light source, a sample enclosure or measurement chamber, an optical interface between the light source, the sample and the detection system, electronics that integrate the light source and the detection system, and computational components, such as an onboard microprocessor for calculation of the gas composition and communications between the sensor and the vehicle electronics. The species-specific gas sensor of the present invention can be used to target gases, such as nitric oxide (NO), nitrogen dioxide (NO.sub.2) ammonia (NH.sub.3), and sulfur dioxide (SO.sub.2) which are measurable in the UV spectrum.

A gas analyzer for measuring two gas components of a measuring gas includes two light-emitting diodes, a beam splitter, a measuring chamber through which the measuring gas circulates, a measurement detector, a reference detector, and a control and evaluation device for controlling the light-emitting diodes in an alternating manner and for evaluating the signals supplied by the measurement detector and the reference detector in terms of measuring results for the two gas components, wherein the beam splitter is arranged in a rectangular metal block, where the measuring chamber is formed as a long hollow body consisting of metal and open on both sides, the measurement detector is held on a detector block consisting of metal, and where the rectangular metal block and the detector block are interconnected via tension rods between which the measuring chamber is clamped.

A gas analyzer via which exhaust gas to be analyzed is conducted untreated through a first measurement chamber and, after treatment in an oxidation device, through a second measurement chamber, wherein ozone is produced from oxygen to thereby convert nitrogen monoxide into nitrogen dioxide, where the gas analyzer has a first light emitting diode and a second light emitting diode, light of both diodes is conducted through the first measurement chamber onto a first detector, light of the first light emitting diode is partly conducted through the second measurement chamber onto a second detector via a beam splitter arrangement, based on the first detector signal, the nitrogen dioxide concentration of the untreated gas is also measured, based on the second detector signal, the nitrogen dioxide concentration of the treated exhaust gas is measured, and the nitrogen oxide concentration of the exhaust gas is additionally determined from measured nitrogen dioxide concentrations.