Factors Contributing to the Ability of Acrolein To Scavenge Corrosive Hydrogen Sulfide

1985 ◽  
Vol 25 (05) ◽  
pp. 647-655 ◽  
Author(s):  
Charles L. Kissel ◽  
John L. Brady ◽  
H. Nancy Clifton Gottry ◽  
Michael J. Meshishnek ◽  
Martin W. Preus

Abstract Acrolein can function under a variety of conditions as an effective hydrogen sulfide scavenger in oilfield waterflood systems. The scavenging ability is maximized in waters having a pH range, of 6 through 8, a total dissolved solids level below 1%, and temperatures less than 149 degrees F [65 degrees C]. At least 4 ppm acrolein is necessary to achieve sufficient reaction of each original 1 ppm hydrogen sulfide. This reaction requires about 2 to 20 minutes, depending on the nature of the system. Although sand, garnet, or diatomaceous earth filters do not affect the scavenging ability of acrolein, charcoal filters, large tanks, long pipelines, high-temperature Wemcos, and reboilers can produce diminished effects. Further diminished effects also can be produced when incompatible chemicals are used concurrently with acrolein. Some application techniques that can lessen or eliminate these adverse conditions are presented. Introduction Hydrogen sulfide has been both a corrosive and a toxic nuisance to oilfield operations for decades. Although an abundance of literature describing the abatement of hydrogen sulfide in gas and drilling mud systems is available, these techniques and environments do not appear to have significant utility in oilfield waterflood operations. Related industries-such as the geothermal, the pulp and paper, and the wastewater industries-appear to pulp and paper, and the wastewater industries-appear to rely on aeration, bacteria chemical scavengers, metallic salt and oxide beds, and oxidizers. Although some of these methods are applicable to oilfield waterflood operations, the majority appear impractical because of cost and compatibility considerations. Specific oilfield waterflood operations have used mechanical and chemical technologies in an attempt to remove hydrogen sulfide from native waters. Some mechanical methods involve aeration, anion exchange resins, degassing, distillation, steam reforming, and zeolite softeners. Most of these methods are viewed currently as being expensive or impractical. Chemical techniques applied to oilfield waterflood operations involve basically the use of neutralizers, oxidizers, and scavengers. Historically, neutralizers-such as sodium hydroxide, ammonia, and amines-were used first in an attempt to remove hydrogen sulfide from produced fluids. These materials are inexpedient because the produced fluids. These materials are inexpedient because the hydrogen sulfide can be easily regenerated within the oilfield waterflood systems when pH changes. Chemical oxidizers can remove hydrogen sulfide from oilfield waterflood operations but can produce undesirable side effects, such as corrosion and the formation of unwanted solids. Examples of oxidizers include chlorine, chlorine dioxide, hypochlorite, hydrogen peroxide, and thiosulfate. peroxide, and thiosulfate. Some attempts to use metallic salts and oxides as scavengers in oilfield waterfloods have resulted in the formation of undesirable solid, metallic sulfides. Metallic salt coatings on zeolite filter agents have been suggested as an alternative. Both formaldehyde and acrolein are aldehydes and are the most frequently used chemical scavengers in oilfield waterflood operations. The use of acrolein to control hydrogen sulfide in aqueous media was commercially available in the 1960's. The general use of aldehydes as additives in acidic media for the suppression of hydrogen sulfide was patented in 1972. A recent publication has compared the ability of some aldehydes to suppress hydrogen sulfide in 10% aqueous sulfuric acid. Under unspecified conditions, some unidentified aldehydes were observed to provide 86 to 98% removal of hydrogen sulfide. Some authors have proposed that aldehydes form thioaldehyde products when treated with hydrogen sulfide. The formation gem-dithiols and 2-thietanol are also reported. But trivinyl-trithiane, a possible product from acrolein, is not reported prominently in the literature. Although thioaldehydes, gem-dithiols, and thietanols might be formed, a more plausible set of reaction products for acrolein is indicated under the conditions products for acrolein is indicated under the conditions normally found in oilfield waterflood systems. SPEJ P. 647

2015 ◽  
Vol 54 (8) ◽  
pp. 3766-3772 ◽  
Author(s):  
Mingtai Sun ◽  
Huan Yu ◽  
Huihui Li ◽  
Hongda Xu ◽  
Dejian Huang ◽  
...  

Holzforschung ◽  
2008 ◽  
Vol 62 (2) ◽  
pp. 169-175 ◽  
Author(s):  
Krishna K. Pandey ◽  
Tapani Vuorinen

Abstract The etherification of phenolic groups has been found to inhibit photodegradation in wood and lignin rich pulps. The precise understanding of kinetics of chemical reaction between lignins or their model compounds and the etherifying agent is the first step for developing a viable modification procedure. In this study, we have investigated the reaction of lignin model compounds (namely, phenol and guaiacol) with propylene oxide in aqueous media. The kinetics of etherification reaction was studied under varying pH conditions in the temperature range 30–60°C. The etherified reaction products were characterized by gas chromatogram-mass spectrum (GC-MS). The extent of etherification of phenols and the rate of chemical reaction was followed by UV-Visible absorption spectroscopy. The reaction between lignin model compounds and propylene oxide was indicated by a rapid reduction in the absorbance accompanied by the development of a new band corresponding to etherified products. The reaction kinetics was investigated at pH ∼12 under the condition of excess concentration of propylene oxide. The reaction followed first order kinetics and rate constants increased linearly with an increase in the temperature and concentration of propylene oxide. The MS fragment data of reaction product support the proposed reaction scheme. The activation energy of the reaction of propylene oxide with phenol and guaiacol, calculated with the Arrhenius equation, was 56.2 kJ mol-1 and 45.4 kJ mol-1, respectively.


2018 ◽  
Vol 21 (9) ◽  
pp. 1248-1258 ◽  
Author(s):  
Hanno C Erythropel ◽  
Sairam V Jabba ◽  
Tamara M DeWinter ◽  
Melissa Mendizabal ◽  
Paul T Anastas ◽  
...  

Abstract Introduction “Vaping” electronic cigarettes (e-cigarettes) is increasingly popular with youth, driven by the wide range of available flavors, often created using flavor aldehydes. The objective of this study was to examine whether flavor aldehydes remain stable in e-cigarette liquids or whether they undergo chemical reactions, forming novel chemical species that may cause harm to the user. Methods Gas chromatography was used to determine concentrations of flavor aldehydes and reaction products in e-liquids and vapor generated from a commercial e-cigarette. Stability of the detected reaction products in aqueous media was monitored by ultraviolet spectroscopy and nuclear magnetic resonance spectroscopy, and their effects on irritant receptors determined by fluorescent calcium imaging in HEK-293T cells. Results Flavor aldehydes including benzaldehyde, cinnamaldehyde, citral, ethylvanillin, and vanillin rapidly reacted with the e-liquid solvent propylene glycol (PG) after mixing, and upward of 40% of flavor aldehyde content was converted to flavor aldehyde PG acetals, which were also detected in commercial e-liquids. Vaping experiments showed carryover rates of 50%–80% of acetals to e-cigarette vapor. Acetals remained stable in physiological aqueous solution, with half-lives above 36 hours, suggesting they persist when inhaled by the user. Acetals activated aldehyde-sensitive TRPA1 irritant receptors and aldehyde-insensitive TRPV1 irritant receptors. Conclusions E-liquids are potentially reactive chemical systems in which new compounds can form after mixing of constituents and during storage, as demonstrated here for flavor aldehyde PG acetals, with unexpected toxicological effects. For regulatory purposes, a rigorous process is advised to monitor the potentially changing composition of e-liquids and e-vapors over time, to identify possible health hazards. Implications This study demonstrates that e-cigarette liquids can be chemically unstable, with reactions occurring between flavorant and solvent components immediately after mixing at room temperature. The resulting compounds have toxicological properties that differ from either the flavorants or solvent components. These findings suggest that the reporting of manufacturing ingredients of e-liquids is insufficient for a safety assessment. The establishment of an analytical workflow to detect newly formed compounds in e-liquids and their potential toxicological effects is imperative for regulatory risk analysis.


1992 ◽  
Author(s):  
Αναστασία Κοτρωναρου

The ultrasonic irradiation of para-nitrophenol, S(-II), and parathion is studied in aqueous solutions at 20 kHz and ~ 75 W-cnT2. Para-nitrophenol was degraded primarily by denitration and secondarily by ΌΗ radical attack to yield N 02, NO3, benzoquinone, hydroquinone, 4-nitrocatechol, formate and oxalate. These reaction products and the kinetic observations are consistent with a model involving high-temperature reactions of p-nitrophenol in the interfa.cia.1 region of cavitation bubbles. The average effective temperature of the interfacial region surrounding the cavitation bubbles was estimated to be T ~ 800 K. Ultrasonic irradiation of S(-II) is studied in aqueous solutions over the pH range 7 - 12. The reaction of HS“ with OH is the principal pathway for theoxidation of S(-II) at pH > 10; the oxidation products are SO2“, SO2", and S20 Upon prolonged sonication, SO2" is the only observed product. At pH < 8.5, thermal decomposition of H2S within or near collapsing cavitation bubbles becomes the important pathway and elemental sulfur is found as an additional product of the sonolysis of S(-II). The sonolytic oxidation of H2S at pH > 10 was successfully modeled with an aqueous-phase free-radical chemistry mechanism and assumingcontinuous and uniform ΌΗ input into solution from the imploding cavitation bubbles. Parathion degradation occurred primarily by enhanced hydrolysis and secondarily by direct ΌΗ radical attack.The effect of various physical and chemical parameters on sonolytic yields is examined. The observed effects are in qualitative agreement with the sonolysis mechanisms proposed for the chemicals of interest and the existing hydrodynamic theories of acoustic cavitation. The formation of iodine upon ultrasonic irradiation of potassium iodide solutions and the sonolysis of S(-II) are used as probes to compare the sonochemical efficiency of different experimental set-ups. This work elucidates the mechanisms of the ultrasonic decomposition of typical organic and inorganic pollutants. It is shown that ultrasound has the potential to become a viable alternative for the destruction of chemical contaminants in water and wastewater. The current limitation of sonolysis is its low energy utilization efficiency, but there is room for improvement by optimizing reactor design and physical/chemical operation conditions. This work offers some recommendations and insight in that respect.


Author(s):  
HENK J. TAKKEN ◽  
LEENDERT M. VAN DER LINDE ◽  
PIETER J. DE VALOIS ◽  
HANS M. VAN DORT ◽  
MANS BOELENS

2010 ◽  
Vol 3 (4) ◽  
pp. 421-428 ◽  
Author(s):  
Scott R. Oneto ◽  
Guy B. Kyser ◽  
Joseph M. DiTomaso

AbstractScotch broom is an invasive leguminous shrub in California and other Pacific Northwest states, as well as New Zealand and Australia. It is highly competitive in forest and shrub communities and can significantly impact reestablishment of conifer forests. The objective of this experiment was to evaluate mechanical methods (Weed Wrench, lopping), several herbicides, and herbicide application techniques for control of Scotch broom in a premontane site in California. Three herbicides were evaluated (glyphosate, imazapyr, and triclopyr ester) for canopy reduction using foliar, drizzle, and basal bark treatments. All treatments were made in both fall and late spring. In addition, we conducted a cost analysis of the various herbicide treatments and application methods. Results indicate that both mechanical treatments were effective, but their optimum timing depended on soil moisture conditions. In addition, there were no significant differences among herbicides at both timings, among all rates, and for any application method. All herbicides provided effective control of Scotch broom. However, the cost analysis demonstrated that the drizzle application method with glyphosate was the most cost-effective treatment, due to low herbicide cost and reduced labor requirements. These results provide several options for Scotch broom control and give land managers considerable flexibility with timing, herbicide, and application technique in their management programs.


1966 ◽  
Vol 49 (6) ◽  
pp. 1180-1183
Author(s):  
Harvey K Hundley ◽  
Duane D Hughes

Abstract Sorbitol is extracted from bakery products with water, and nonreducing sugars are inverted by acid hydrolysis. Carbohydrates other than the sugar alcohols are degraded in alkaline solution and reaction products are removed by ion exchange resins. Sorbitol is determined by the amount of periodate consumed in oxidation and identified by thin layer chromatography.


RSC Advances ◽  
2018 ◽  
Vol 8 (22) ◽  
pp. 12043-12052 ◽  
Author(s):  
Simarpreet Kaur ◽  
Ivan Kempson ◽  
Haolan Xu ◽  
Magnus Nydén ◽  
Mikael Larsson

Porous ion-exchange resins with features of high selectivity, high capacity, fast adsorption kinetics and chemical stability over a wide pH range are attractive for extracting precious metals like copper and upcycling waste.


2015 ◽  
Vol 39 (7) ◽  
pp. 5669-5675 ◽  
Author(s):  
Avijit Kumar Das ◽  
Shyamaprosad Goswami ◽  
Ching Kheng Quah ◽  
Hoong-Kun Fun

Ratiometric and fast detection of H2S via NGP of thiol rather than direct nucleophilic attack to cleave active ether linkage.


1976 ◽  
Vol 153 (1) ◽  
pp. 119-126 ◽  
Author(s):  
D E Woolley ◽  
J S Tucker ◽  
G Green ◽  
J M Evanson

Biopsy specimens of human gastric mucosa, maintained in culture for 7 days in the absence of serum, released a collagen-degrading enzyme into the medium. The yield of active enzyme reached a maximum after 2-3 days, and viable tissue, capable of protein synthesis, was essential for its production. 2. At 25 degrees C the enzyme attacked undenatured collagen in solution, resulting in a 55% loss of specific viscosity and producing the two products TCA and TCB characteristic of neutral-collagenase action. 3. Electron microscopy of segment-long-spacing crystallites of these reaction products showed the exact cleavage locus of the collagen molecules to be between bands 43 and 44 (I-43). The larger TCA and smaller TCB products were fragments representing 77 and 23% respectively of the length of the collagen molecule. 4. Optimal enzyme activity was observed over the pH range 7.5-8.5 and a mol.wt. of approx. 38000 was derived from gel-filtration studies. 5. The enzyme was shown to be inhibited by the human serum proteins ²2-macroglobulin and a smaller component of mol.wt. approx. 40000; α1-anti-trypsin was not inhibitory. 6. EDTA, 1, 10-phenanthroline, cysteine and dithiothreitol all inhibited collagenase activity. 7. The gastric enzyme has properties similar to other well characterized collagenases, but differences exist with respect to its molecular size and the site of attack on the collagen molecule.


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