scholarly journals Evaluation of Single Column Trapping/Separation and Chemiluminescence Detection for Measurement of Methanethiol and Dimethyl Sulfide from Pig Production

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Michael Jørgen Hansen ◽  
Kei Toda ◽  
Tomoaki Obata ◽  
Anders Peter S. Adamsen ◽  
Anders Feilberg
Keyword(s):  
Hydrogen Sulfide ◽  
Silica Gel ◽  
Dimethyl Sulfide ◽  
Low Cost ◽  
Proton Transfer Reaction ◽  
Chemiluminescence Detection ◽  
High Concentration ◽  
Reduced Sulfur Compounds ◽  
Pig Production ◽  
The Difference

Reduced sulfur compounds are considered to be important odorants from pig production due to their low odor threshold values and low solubility in slurry. The objective of the present study was to investigate the use of a portable method with a single silica gel column for trapping/separation coupled with chemiluminescence detection (SCTS-CL) for measurement of methanethiol and dimethyl sulfide in sample air from pig production. Proton-transfer-reaction mass spectrometry (PTR-MS) was used to evaluate the trapping/separation. The silica gel column used for the SCTS-CL efficiently collected hydrogen sulfide, methanethiol and dimethyl sulfide. The measurement of methanethiol by SCTS-CL was clearly interfered by the high concentration of hydrogen sulfide found in pig production, and a removal of hydrogen sulfide was necessary to obtain reliable results. Air samples taken from a facility with growing-finishing pigs were analyzed by SCTS-CL, PTR-MS, and a gas chromatograph with sulfur chemiluminescence detection (GC-SCD) to evaluate the SCTS-CL. The difference between the concentrations of methanethiol and dimethyl sulfide measured with SCTS-CL, PTR-MS, and GC-SCD was below 10%. In conclusion, the SCTS-CL is a portable and low-cost alternative to the commercial methods that can be used to measure methanethiol and dimethyl sulfide in sample air from pig production.

scholarly journals Seasonal and interannual study of volatile reduced sulfur compounds (VRSC) in coastal environment: the Bay of Quiberon (Brittany, France)

2009 ◽  
Vol 6 (5) ◽  
pp. 10057-10088 ◽  
Author(s):  
A. Cozic-Houly ◽  
E. Viollier ◽  
G. Sarazin ◽  
J. Knoery
Keyword(s):  
Hydrogen Sulfide ◽  
Water Column ◽  
Seasonal Variations ◽  
Dimethyl Sulfide ◽  
Carbonyl Sulfide ◽  
Dimethyl Disulfide ◽  
Coastal Environment ◽  
Water Interface ◽  
Reduced Sulfur Compounds ◽  
Coastal Marine

Abstract. Seasonal and annual variability of hydrogen sulfide (H2S), carbonyl sulfide (OCS), methane thiol (MeSH), dimethyl sulfide (DMS) and dimethyl disulfide (DMDS) concentrations and supporting parameters (e.g., phytoplanktonic cells abundance) were investigated in a coastal marine environment, the Bay of Quiberon (Brittany, France) from July 2004 to August 2006. The sampling was conducted in the water column, within two meters of the sediment water interface (SWI). Minimum and maximum values were <0.1–1.6 nmol L−1 for H2S, <0.1–4.2 nmol L−1 for OCS, <0.1–7.8 nmol L−1 for MeSH, <0.1–17.5 nmol L−1 for DMS and <0.1–1.7 nmol L−1 for DMDS. Vertical carbonyl sulfide distribution showed seasonal variations with lower concentration near the SWI in winter and bottom enrichments near sediments in summer. Vertical sulfide distribution not seems to be influenced by the shallow sediments. The likely influence of Dinophyceae abundance on the MeSH, DMS and DMDS concentrations was evident for the 3-summer monitored period.

Successful Lifting of Oil with High Concentration of Hydrogen Sulfide by Artificial Lift System – Case Study

2021 ◽  
Author(s):  
Abid Ur Rehman ◽  
Marwan Abdelbary
Keyword(s):  
Hydrogen Sulfide ◽  
Low Cost ◽  
Decisive Role ◽  
High Concentration ◽  
Jet Pump ◽  
Pump System ◽  
Northern Iraq ◽  
Well Completion ◽  
Artificial Lift ◽  
Single Well

Abstract Due to the low cost of crude oil, it is highly unusual for the operators to drill exploration wells, for the past few years. Adding that as well to the world's economy collapse due to the pandemic at the start of 2020, it is now more than ever a necessity to use artificial lift methods to lift from previously shut-in wells or maximize current production of the wells, as to grapple with the running expenses of operators. The artificial lift is a vast field with different lift methods applicable to a single well. Hence, the selection of an optimum lift method is critical. During the worst economic slump, the economic analysis will play a decisive role in the application of an artificial lift system (ALS) along with a technical review. The jet pump system is one of the most reliable artificial lift systems for lifting shut-in wells. The installation time of this system is minimal, and production starts right away. However, the system can prove to be very expensive, if the design is not done critically. This paper is about lifting a well that was not able to flow naturally. The vertical well B3 located in northern Iraq was drilled in May 2018 to a total depth of 521 meters. But the well was not able to flow naturally, and the jet pump was designed for the well based on well completion, downhole pressures, temperature and reservoir fluid properties. The evaluation and design of the downhole jet pump and surface pumping unit requirements were performed on Jet Pump Evaluation and Modeling Software. This well produced approximately 1700 BOPD. Since, the well was not flowing before the installation of the jet pump, most of the production data was obtained after deployment of ALS and production was optimized accordingly. The production had a high content of Hydrogen Sulfide as well, which was treated accordingly for safety of personnel, equipment, flow lines and environment. This paper describes the details about the application, optimization and operation of the jet pump system deployed on inactive wells with a high concentration of sour gas.

Biofiltration of hydrogen sulfide by Sulfolobus metallicus at high temperatures

2012 ◽  
Vol 66 (9) ◽  
pp. 1958-1961 ◽  
Author(s):  
M. Morales ◽  
J. Silva ◽  
P. Morales ◽  
J. C. Gentina ◽  
G. Aroca
Keyword(s):  
Hydrogen Sulfide ◽  
High Temperatures ◽  
Sulfur Removal ◽  
Sulfur Compounds ◽  
Residence Times ◽  
Reduced Sulfur Compounds ◽  
Removal Capacity ◽  
Industrial Sectors ◽  
Different Temperatures ◽  
The Difference

Biofiltration of reduced sulfur compounds such as hydrogen sulfide has been mainly applied to emissions at mild temperatures (25 to 35 °C). However, an important number of industrial gaseous emission containing sulfur compounds, from diverse industrial sectors (petroleum refinery, cellulose production, smelting, rendering plants and food industries) are emitted at temperatures over 50 °C. Most of the studies on thermophilic systems report that a higher elimination capacity can be obtained at elevated temperature, allowing the design of smaller equipment for the same loading rate than that required for removing the same load under mesophilic conditions. A biotrickling filter inoculated with Sulfolobus metallicus, which operates at three different residence times, 60, 80 and 120 s, and two different temperatures (45 and 55 °C) for treating H2S is reported. The input loads of H2S were progressively increased from 0 to 100 gS/m3. The aim of this study was to determine the capacity and ability of S. metallicus to oxidize H2S at high temperatures. The better removal capacity of H2S obtained was 37.1 ± 1.7 gS/m3 h at 55 °C for a residence time of 120 s. The difference of the removal capacity of H2S between the two temperatures was 4 g/m3 h on average of sulfur removal for the different residence times.

Tem analysis of multiple-energy arsenic implanted and Rta'd silicon

1987 ◽  
Vol 45 ◽  
pp. 246-247
Author(s):  
R.A. Herring
Keyword(s):  
Device Fabrication ◽  
High Concentration ◽  
Tem Analysis ◽  
Defect Clusters ◽  
High Fluences ◽  
Small Defect ◽  
Before And After ◽  
The Matrix ◽  
The Difference ◽  
Factor Type

Rapid thermal annealing (RTA) of ion-implanted Si is important for device fabrication. The defect structures of 2.5, 4.0, and 6.0 MeV As-implanted silicon irradiated to fluences of 2E14, 4E14, and 6E14, respectively, have been analyzed by electron diffraction both before and after RTA at 1100°C for 10 seconds. At such high fluences and energies the implanted As ions change the Si from crystalline to amorphous. Three distinct amorphous regions emerge due to the three implantation energies used (Fig. 1). The amorphous regions are separated from each other by crystalline Si (marked L1, L2, and L3 in Fig. 1) which contains a high concentration of small defect clusters. The small defect clusters were similar to what had been determined earlier as being amorphous zones since their contrast was principally of the structure-factor type that arises due to the difference in extinction distance between the matrix and damage regions.

scholarly journals Spatial Analysis (Measurements at Heights of 10 m and 20 m above Ground Level) of the Concentrations of Particulate Matter (PM10, PM2.5, and PM1.0) and Gaseous Pollutants (H2S) on the University Campus: A Case Study

Atmosphere ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 62
Author(s):  
Robert Cichowicz ◽  
Maciej Dobrzański
Keyword(s):  
Spatial Distribution ◽  
Hydrogen Sulfide ◽  
Particulate Matter ◽  
Air Quality ◽  
Spatial Analysis ◽  
Ground Level ◽  
Leeward Side ◽  
High Concentration ◽  
Above Ground Level ◽  
High Concentrations

Spatial analysis of the distribution of particulate matter PM10, PM2.5, PM1.0, and hydrogen sulfide (H2S) gas pollution was performed in the area around a university library building. The reasons for the subject matter were reports related to the perceptible odor characteristic of hydrogen sulfide and a general poor assessment of air quality by employees and students. Due to the area of analysis, it was decided to perform measurements at two heights, 10 m and 20 m above ground level, using measuring equipment attached to a DJI Matrice 600 unmanned aerial vehicle (UAV). The aim of the measurements was air quality assessment and investigate the convergence of the theory of air flow around the building with the spatial distribution of air pollutants. Considerable differences of up to 63% were observed in the concentrations of pollutants measured around the building, especially between opposite sides, depending on the direction of the wind. To explain these differences, the theory of aerodynamics was applied to visualize the probable airflow in the direction of the wind. A strong convergence was observed between the aerodynamic model and the spatial distribution of pollutants. This was evidenced by the high concentrations of dust in the areas of strong turbulence at the edges of the building and on the leeward side. The accumulation of pollutants was also clearly noticeable in these locations. A high concentration of H2S was recorded around the library building on the side of the car park. On the other hand, the air turbulence around the building dispersed the gas pollution, causing the concentration of H2S to drop on the leeward side. It was confirmed that in some analyzed areas the permissible concentration of H2S was exceeded.

Improved photocatalytic conversion of high−concentration ammonia in water by low−cost Cu/TiO2 and its mechanism study

Chemosphere ◽  
2021 ◽  
Vol 274 ◽  
pp. 129689
Author(s):  
Jianpei Feng ◽  
Xiaolei Zhang ◽  
Guan Zhang ◽  
Ji Li ◽  
Wei Song ◽  
...  
Keyword(s):  
Low Cost ◽  
Mechanism Study ◽  
High Concentration

scholarly journals Synthesis of poly (n-butyl acrylate) with tempo by nitroxide mediated polymerization method

2021 ◽  
pp. 096739112110245
Author(s):  
Amrita Sharma ◽  
PP Pande
Keyword(s):  
Butyl Acrylate ◽  
Low Cost ◽  
Polymerization Process ◽  
Polymerization Reaction ◽  
High Concentration ◽  
Acrylate Monomer ◽  
Controlled Polymerization ◽  
Acrylate Monomers ◽  
Nitroxide Mediated Polymerization ◽  
Polymerization Method

It has been observed that acrylate monomers are very difficult to polymerize with the low cost nitroxide catalyst 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO). Therefore, costly acyclic nitroxides such as N-tert-butyl-N-(1-diethylphosphono-2,2-dimethyl)-N-oxyl, (SG1), 2,2,5-Trimethyl-4-phenyl-3-azahexane-3-nitroxide (TIPNO) and TIPNO derivatives have to be used for the polymerization of the acrylic acid derivatives. There are very few reports on the use of TEMPO-derivatives toward the polymerization of n-butyl acrylate. Generally different reducing agents viz. glucose, ascorbic acid, hydroxyacetone etc. have been used to destroy excess TEMPO during the polymerization reaction. The acrylate polymerizations fail in the presence of TEMPO due to the strong C–O bond formed between the acrylate chain end and nitroxide. To the best of our knowledge, no literature report is available on the use of TEMPO without reducing agent or high temperature initiators, toward the polymerization of n-butyl acrylate. The present study has been carried out with a view to re-examine the application of low cost nitroxide TEMPO, so that it can be utilized towards the polymerization of acrylate monomers (e.g. n-butyl acrylate). We have been able to polymerize n-butyl acrylate using the nitroxide TEMPO as initiator (via a macroinitiator). In this synthesis, a polystyrene macroinitiator was synthesized in the first step from TEMPO, after this TEMPO end-capped styrene macroinitiator (PSt-TEMPO) is used to polymerize n-butyl acrylate monomer. The amount of macroinitiator taken was varied from 0.05% to 50% by weight of n-butyl acrylate monomer. The polymerization was carried out at 120°C by bulk polymerization method. The experimental findings showed a gradual increase in molecular weight of the polymer formed and decrease in the polydispersity index (PDI) with increase in amount of PSt-TEMPO macroinitiator taken. In all experiments conversion was more than 80%. These results indicate that the polymerization takes place through controlled polymerization process. Effect of different solvents on polymerization has also been investigated. In the following experiments TEMPO capped styrene has been used as macroinitiator leading to the successful synthesis of poly n-Butyl acrylate. It has been found that styrene macroinitiator is highly efficient for the nitroxide mediated polymerization, even in very small concentration for the synthesis of poly n-butyl acrylate. High concentration of macroinitiator results in the formation of block copolymers of polystyrene and poly ( n-butyl acrylate) viz. polystyrene-block-poly-( n-butyl acrylate). The use of TEMPO toward controlled polymerization is of much importance, because it is the nitroxide commercially available at the lowest cost.

scholarly journals Molecularly imprinted electrospun fiber membrane for colorimetric detection of hexanoic acid

e-Polymers ◽  
2021 ◽  
Vol 21 (1) ◽  
pp. 500-510
Author(s):  
Xiaoguang Ying ◽  
Jieyuan He ◽  
Xiao Li
Keyword(s):  
Low Cost ◽  
Electrospun Fiber ◽  
Colorimetric Detection ◽  
Hexanoic Acid ◽  
Bromocresol Purple ◽  
Fiber Membrane ◽  
Color Changes ◽  
Before And After ◽  
The Difference ◽  
Imagej Software

Abstract An imprinted electrospun fiber membrane was developed for the detection of volatile organic acids, which are key components of human body odor. In this study, hexanoic acid (HA) was selected as the target, polymethyl methacrylate (PMMA) was used as the substrate, and colorimetric detection of HA was achieved by a bromocresol purple (BCP) chromogenic agent. The results showed that the morphology of the fiber membrane was uniform and continuous, and it showed excellent selectivity and specificity to HA. Photographs of the color changes before and after fiber membrane adsorption were recorded by a camera and quantified by ImageJ software by the difference in gray value (ΔGray). This method is simple, intuitive, and low cost and has great potential for application in human odor analysis.

scholarly journals Quantitative Analysis of Fluorescence Detection Using a Smartphone Camera for a PCR Chip

Sensors ◽  
2021 ◽  
Vol 21 (11) ◽  
pp. 3917
Author(s):  
Jong-Dae Kim ◽  
Chan-Young Park ◽  
Yu-Seop Kim ◽  
Ji-Soo Hwang
Keyword(s):  
Quantitative Analysis ◽  
Fluorescence Detection ◽  
High Performance ◽  
Low Cost ◽  
Dna Amplification ◽  
Fluorescent Detection ◽  
Rt Pcr ◽  
Commercial System ◽  
Intensity Changes ◽  
The Difference

Most existing commercial real-time polymerase chain reaction (RT-PCR) instruments are bulky because they contain expensive fluorescent detection sensors or complex optical structures. In this paper, we propose an RT-PCR system using a camera module for smartphones that is an ultra small, high-performance and low-cost sensor for fluorescence detection. The proposed system provides stable DNA amplification. A quantitative analysis of fluorescence intensity changes shows the camera’s performance compared with that of commercial instruments. Changes in the performance between the experiments and the sets were also observed based on the threshold cycle values in a commercial RT-PCR system. The overall difference in the measured threshold cycles between the commercial system and the proposed camera was only 0.76 cycles, verifying the performance of the proposed system. The set calibration even reduced the difference to 0.41 cycles, which was less than the experimental variation in the commercial system, and there was no difference in performance.

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