Non-Toxic Environment for Ferritic Nitrocarburising Process

2018 ◽  
Vol 69 (9) ◽  
pp. 2416-2419
Author(s):  
Mihai Branzei ◽  
Mihai Ovidiu Cojocaru ◽  
Leontin Nicolae Druga ◽  
Florica Tudose ◽  
Roxana Trusca
Keyword(s):  
Surface Reaction ◽  
Effective Solution ◽  
Reaction Products ◽  
Toxic Reaction ◽  
Wide Range ◽  
Toxic Environment ◽  
Thermochemical Processing ◽  
Surface Saturation ◽  
Gas Molecules ◽  
Toxic Components

Experimental research aimed to find a solution for replacing components with high toxicity (or generating such components as a result of reactions occurring in the environment at processing temperatures) from the environments used for ferritic nitrocarburising process (FNCP) with non-hazardous components, but extremely active during the process. In the temperature range in which this type of processing is applied (lower than the eutectoid transformation temperature in the Fe-N phase diagram), the most commonly used media are liquid or gaseous; liquid ones contain toxic components (sodium or potassium cyanates/cyanides), and gaseous ones require complex equipments. Packing is extremely rarely used, but in this case pack-mix contain toxic components (15 � 20 wt.% sodium or potassium ferrocyanide). Urea also called carbamide (CO (NH2)2) is the active component in the pack-mixing proposed to be used for FNCP. Carbamide is used in low temperature cyanidation thermochemical heat treatment (liquid FNC), together with sodium or potassium carbonates, resulting in very toxic reaction products (sodium or potassium cyanates). Compared to cyanidation, in the version proposed in the paper, the carbamide does not react with carbonates because they are not found in the composition of the environment but decomposes in the presence or absence of oxygen (by a disproportionation reaction) with the formation of some gas molecules interesting for the process. It has been concluded that the use of carbamide together with two other components, activated charcoal (having a triple role - dispersing, storage, surface saturation) and respectively ammonium chloride as surface reaction activator, is an effective solution for achieving the desired goals by applying this type of thermochemical processing to a wide range of products made of quality steels up to alloy miscellaneous steels.

scholarly journals Formation of flavorant–propylene Glycol Adducts With Novel Toxicological Properties in Chemically Unstable E-Cigarette Liquids

2018 ◽  
Vol 21 (9) ◽  
pp. 1248-1258 ◽  
Author(s):  
Hanno C Erythropel ◽  
Sairam V Jabba ◽  
Tamara M DeWinter ◽  
Melissa Mendizabal ◽  
Paul T Anastas ◽  
...  
Keyword(s):  
Propylene Glycol ◽  
Electronic Cigarettes ◽  
Aqueous Media ◽  
Chemical Species ◽  
Resonance Spectroscopy ◽  
Reaction Products ◽  
Chemical Systems ◽  
Toxicological Effects ◽  
Wide Range ◽  
Irritant Receptors

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.

scholarly journals Emission of Noble Gases Binary Mixtures under Excitation by the Products of the 6Li (n, α)3 H Nuclear Reaction

2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Kuanysh Samarkhanov ◽  
Mendykhan Khasenov ◽  
Erlan Batyrbekov ◽  
Inesh Kenzhina ◽  
Yerzhan Sapatayev ◽  
...  
Keyword(s):  
Nuclear Reaction ◽  
Nuclear Energy ◽  
Alkali Metals ◽  
Nuclear Reactor ◽  
Noble Gases ◽  
Noble Gas ◽  
Direct Conversion ◽  
Reaction Products ◽  
Gas Molecules ◽  
Sodium And Potassium

The luminescence of Kr-Xe, Ar-Kr, and Ar-Xe mixtures was studied in the spectral range 300–970 nm when excited by 6Li (n, α)3 H nuclear reaction products in the core of a nuclear reactor. Lithium was deposited on walls of experimental cell in the form of a capillary-porous structure, which made it possible to measure up to a temperature of 730 K. The temperature dependence of the radiation intensity of noble gas atoms, alkali metals, and heteronuclear ionic noble gas molecules was studied. Also, as in the case of single-component gases, the appearance of lithium lines and impurities of sodium and potassium is associated with vaporization during the release of nuclear reaction products from the lithium layer. The excitation of lithium atoms occurs mainly as a result of the Penning process of lithium atoms on noble gas atoms in the 1s states and subsequent ion-molecular reactions. Simultaneous radiation at transitions of atoms of noble gases and lithium, heteronuclear ion molecules of noble gases allows us to increase the efficiency of direct conversion of nuclear energy into light.

scholarly journals Methane-induced haemolysis of human erythrocytes

1995 ◽  
Vol 307 (2) ◽  
pp. 433-438 ◽  
Author(s):  
H Batliwala ◽  
T Somasundaram ◽  
E E Uzgiris ◽  
L Makowski
Keyword(s):  
Diffusion Rate ◽  
Human Erythrocytes ◽  
Experimental Conditions ◽  
Detergent Concentration ◽  
Partial Pressures ◽  
Temperature Diffusion ◽  
Wide Range ◽  
Gas Molecules ◽  
High Concentrations ◽  
Cell Leakage

Human erythrocytes were exposed to high concentrations of methane and nitrogen through the application of elevated partial pressures of these gas molecules. Cell leakage (haemolysis) was measured for cells exposed to these gases under a wide range of experimental conditions. Application of methane produces haemolysis at pressures far below the hydrostatic pressures known to disrupt membrane or protein structure. The effects of changes in buffer, temperature, diffusion rate and detergents were studied. Methane acts co-operatively with detergents to produce haemolysis at much lower detergent concentration than is required in the absence of methane or in the presence of nitrogen. At sufficiently high concentrations of methane, all cells are haemolysed. Increased temperature enhances the effect. Methane produces 50% haemolysis at a concentration of about 0.33 M compared with about 7.5 M methanol required for the same degree of haemolysis.

scholarly journals Terpenes and their oxidation products in the French Landes forest: insights from Vocus PTR-TOF measurements

2020 ◽  
Vol 20 (4) ◽  
pp. 1941-1959 ◽  
Author(s):  
Haiyan Li ◽  
Matthieu Riva ◽  
Pekka Rantala ◽  
Liine Heikkinen ◽  
Kaspar Daellenbach ◽  
...  
Keyword(s):  
Gas Phase ◽  
Detection Efficiency ◽  
Ambient Air ◽  
Reaction Rates ◽  
Early Morning ◽  
Oxidation Products ◽  
Atmospheric Oxidation ◽  
Organic Nitrates ◽  
Reaction Products ◽  
Wide Range

Abstract. The capabilities of the recently developed Vocus proton-transfer-reaction time-of-flight mass spectrometer (PTR-TOF) are reported for the first time based on ambient measurements. With the deployment of the Vocus PTR-TOF, we present an overview of the observed gas-phase (oxygenated) molecules in the French Landes forest during summertime 2018 and gain insights into the atmospheric oxidation of terpenes, which are emitted in large quantities in the atmosphere and play important roles in secondary organic aerosol production. Due to the greatly improved detection efficiency compared to conventional PTR instruments, the Vocus PTR-TOF identifies a large number of gas-phase signals with elemental composition categories including CH, CHO, CHN, CHS, CHON, CHOS, and others. Multiple hydrocarbons are detected, with carbon numbers up to 20. Particularly, we report the first direct observations of low-volatility diterpenes in the ambient air. The diurnal cycle of diterpenes is similar to that of monoterpenes and sesquiterpenes but contrary to that of isoprene. Various types of terpene reaction products and intermediates are also characterized. Generally, the more oxidized products from terpene oxidations show a broad peak in the day due to the strong photochemical effects, while the less oxygenated products peak in the early morning and/or in the evening. To evaluate the importance of different formation pathways in terpene chemistry, the reaction rates of terpenes with main oxidants (i.e., hydroxyl radical, OH; ozone, O3; and nitrate radical, NO3) are calculated. For the less oxidized non-nitrate monoterpene oxidation products, their morning and evening peaks have contributions from both O3- and OH-initiated monoterpene oxidation. For the monoterpene-derived organic nitrates, oxidations by O3, OH, and NO3 radicals all contribute to their formation, with their relative roles varying considerably over the course of the day. Through a detailed analysis of terpene chemistry, this study demonstrates the capability of the Vocus PTR-TOF in the detection of a wide range of oxidized reaction products in ambient and remote conditions, which highlights its importance in investigating atmospheric oxidation processes.

Statistical Study of the Effect of the Composition on the Strength of Supersulphated Cements

2013 ◽  
Vol 1612 ◽  
Author(s):  
Y.B. Castillo-Sánchez ◽  
J.M. Almanza-Robles ◽  
J.I. Escalante-García
Keyword(s):  
Portland Cement ◽  
Raw Materials ◽  
Optimal Conditions ◽  
Reaction Products ◽  
X Ray Diffraction ◽  
Wide Range ◽  
Dense Matrices ◽  
Alkaline Activator ◽  
Furnace Slag ◽  
Effect Of The Composition

ABSTRACTSupersulphated cements (SSC) are environmentally friendly binders that incorporate several raw materials, including byproducts. A systematic study was considered opportune considering the wide range of formulations found in the literature. The effect of the type and proportioning of components in the strength of SC was investigated using the Taguchi method to optimize the experimental work and to define the optimal conditions. The factors were: [A] %blast furnace slag (82.5-90%), [B] CaSO4 - alkaline activator ratio (1:0, 3:1, 1:1, 1:3 and 0:1), [C] type of CaSO4 (5 types) and [D] type of alkaline activator (portland cement, Ca(OH)2, KOH and NaCO3 and 2 combinations of these). Pastes were prepared and characterized for up to 28 days at 20°C. In general, for all values of [A] the best strength was for levels of [C] at 3:1, followed by the 1:1 and 1:0 ratios. The optimal conditions using the 28 day strength consisted of [A]= 82.5%, [B]= 3:1, [C]= flyorgypsum and [D] = portland cement, which developed excellent strength from day one and 35MPa. X-ray diffraction showed ettringite and C-S-H formation from the early ages. The microstructures showed dense matrices of reaction products well bonded to partially reacted slag grains, which in some cases showed rims of hydration products.

Alkyne oxidation I. Acetylene oxidation

1970 ◽  
Vol 317 (1528) ◽  
pp. 1-20 ◽  
Keyword(s):  
Main Chain ◽  
Initial Pressure ◽  
Ion Source ◽  
Reaction Products ◽  
Experimental Conditions ◽  
Ethynyl Radical ◽  
Wide Range ◽  
Slow Combustion ◽  
To Come ◽  
Isotopic Mixing

The slow combustion of acetylene has been studied analytically and kinetically over a wide range of experimental conditions by continually sampling the reactants and products through a pinhole leak in a Pyrex reaction vessel into the ion source of a quadrupole mass spectrometer. The mass spectra were interpreted and the reaction products identified with the help of labelled acetylene (C 2 D 2 ) and oxygen ( 18 O 2 ). There is no incubation period in the disappearance of the reactants and the formation of glyoxal in the early stages of reaction gives the initial pressure drop. The addition of glyoxal has no effect on the reaction. The products of the reaction and their kinetic orders with respect to acetylene are, carbon monoxide (2.0), carbon dioxide (2.0), water (2.3), hydrogen (1.7), glyoxal (2.5-shown by labelling experiments to be produced from one acetylene and two oxygen molecules), form aldehyde (1.9), acetaldehyde (shown to come from wall catalysed rearrangement of vinyl alcohol), acrolein, keten, formic acid (2.25), acetic acid (2.25-shown by isotopic experiments to come from acetaldehyde), methanol and hydrogen peroxide. The consumption of acetylene and oxygen are dependent on the second power of the acetylene concentration and the reaction is largely independent of the concentration of oxygen and incrt gases. Isotopic mixing occurs in mixtures of acetylene and dideuterio-acetylene by way of ethynyl radical reactions. The reaction is suggested to be initiated by reaction between two acetylene molecules and terminated by the interaction of two hydroperoxyl radicals. The main chain produces the intermediate products glyoxal, form aldehyde and keten, the first being produced to a higher order and the second two to a lower order dependence on acetylene concentration than the rate of removal of acetylene. Two mechanisms are considered to account for the kinetics, the first involving conversion of hydroperoxyl to hydroxyl which acts as the main chain carrier and the second involving both hydroxyl and hydroperoxyl as chain carriers.

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