scholarly journals Synergistic Effects of Multiple Environmental Factors on Degradation of Hydrogenated Nitrile Rubber Seals

Polymers ◽  
2018 ◽  
Vol 10 (8) ◽  
pp. 897 ◽  
Author(s):  
Weitao Lou ◽  
Weifang Zhang ◽  
Tingzhu Jin ◽  
Xuerong Liu ◽  
Wei Dai
Keyword(s):  
Environmental Factors ◽  
Elevated Temperatures ◽  
Synergistic Effects ◽  
Degradation Process ◽  
Nitrile Rubber ◽  
Oxidation Products ◽  
Compression Stress ◽  
Hydraulic Systems ◽  
Hydraulic Oil ◽  
Higher Temperature

Degradation tests of hydrogenated nitrile rubber seals, often used as sealing components in hydraulic systems, were conducted under the free and compression state in air and hydraulic oil at three elevated temperatures for several days to investigate the synergistic effects among three factors. The crosslinking and chain scission reactions both occurred simultaneously at higher temperature during the degradation process, and crosslinking predominated for most cases. Additionally, the synergistic effect between compression stress and hydraulic oil further slowed the degradation rate by limiting oxygen access. However, the higher temperature and hydraulic oil both promoted the formation of oxidation products, whereas the compression stress restrained the formation of amide groups. The fracture morphology results show that the defects gradually formed on the fracture surface, especially for the uncompressed specimens. The increase of the compression set aged in air was more than that in hydraulic oil, implying the more serious degradation. Moreover, rubber seals under the synthetic effect of three environmental factors presented the minimum degradation level. The degradation of the compressed and uncompressed specimens exposed to hydraulic oil is more serious than that of specimens exposed to air.

scholarly journals Photocatalytic Pretreatment of Commercial Lignin Using TiO2-ZnO Nanocomposite-Derived Advanced Oxidation Processes for Methane Production Synergy in Lab Scale Continuous Reactors

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 54
Author(s):  
Yu-Ming Chu ◽  
Hafiz Muhammad Asif Javed ◽  
Muhammad Awais ◽  
Muhammad Ijaz Khan ◽  
Sana Shafqat ◽  
...  
Keyword(s):  
Photocatalytic Oxidation ◽  
Advanced Oxidation Processes ◽  
Synergistic Effects ◽  
Oxidation Products ◽  
Methane Yield ◽  
Zno Nanoparticle ◽  
Coumaric Acid ◽  
Stirred Tank Reactors ◽  
Lignin Oxidation ◽  
Constant Operation

The photocatalytic pretreatment of lignocellulosic biomass to oxidize lignin and increase biomass stability has gained attention during the last few years. Conventional pretreatment methods are limited by the fact that they are expensive, non-renewable and contaminate the anaerobic digestate later on. The present study was focused to develop a metal-derived photocatalyst that can work with visible electromagnetic spectra light and oxidize commercial lignin liquor. During this project the advanced photocatalytic oxidation of lignin was achieved by using a quartz cube tungsten T3 Halogen 100 W lamp with a laboratory manufactured TiO2-ZnO nanoparticle (nanocomposite) in a self-designed apparatus. The products of lignin oxidation were confirmed to be vanillic acid (9.71 ± 0.23 mg/L), ferrulic acid (7.34 ± 0.16 mg/L), benzoic acid (6.12 ± 0.17 mg/L) and p-coumaric acid (3.80 ± 0.13 mg/L). These all products corresponded to 85% of the lignin oxidation products that were detectable, which is significantly more than any previously reported lignin pretreatment with even more intensity. Furthermore, all the pretreatment samples were supplemented in the form of feedstock diluent in uniformly operating continuously stirred tank reactors (CSTRs). The results of pretreatment revealed 85% lignin oxidation and later on these products did not hinder the CSTR performance at any stage. Moreover, the synergistic effects of pretreated lignin diluent were seen that resulted in 39% significant increase in the methane yield of the CSTR with constant operation. Finally, the visible light and nanoparticles alone could not pretreat lignin and when used as diluent, halted and reduced the methane yield by 37% during 4th HRT.

scholarly journals Gene–gene and gene-environment interactions on cord blood total IgE in Chinese Han children

2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Li Hua ◽  
Quanhua Liu ◽  
Jing Li ◽  
Xianbo Zuo ◽  
Qian Chen ◽  
...  
Keyword(s):  
Environmental Factors ◽  
Cord Blood ◽  
Synergistic Effects ◽  
Gene Interaction ◽  
Independent Effect ◽  
Environment Interaction ◽  
Nucleotide Polymorphisms ◽  
Chinese Han ◽  
Gene Environment Interaction ◽  
Gene Environment

Abstract Background IL13, IL4, IL4RA, FCER1B and ADRB2 are susceptible genes of asthma and atopy. Our previous study has found gene–gene interactions on asthma between these genes in Chinese Han children. Whether the interactions begin in fetal stage, and whether these genes interact with prenatal environment to enhance cord blood IgE (CBIgE) levels and then cause subsequent allergic diseases have yet to be determined. This study aimed to determine whether there are gene–gene and gene-environment interactions on CBIgE elevation among the aforementioned five genes and prenatal environmental factors in Chinese Han population. Methods 989 cord blood samples from a Chinese birth cohort were genotyped for nine single-nucleotide polymorphisms (SNPs) in the five genes, and measured for CBIgE levels. Prenatal environmental factors were collected using a questionnaire. Gene–gene and gene-environment interactions were analyzed with generalized multifactor dimensionality methods. Results A four-way gene–gene interaction model (IL13 rs20541, IL13 rs1800925, IL4 rs2243250 and ADRB2 rs1042713) was regarded as the optimal one for CBIgE elevation (testing balanced accuracy = 0.5805, P = 9.03 × 10–4). Among the four SNPs, only IL13 rs20541 was identified to have an independent effect on elevated CBIgE (odds ratio (OR) = 1.36, P = 3.57 × 10–3), while the other three had small but synergistic effects. Carriers of IL13 rs20541 TT, IL13 rs1800925 CT/TT, IL4 rs2243250 TT and ADRB2 rs1042713 AA were estimated to be at more than fourfold higher risk for CBIgE elevation (OR = 4.14, P = 2.69 × 10–2). Gene-environment interaction on elevated CBIgE was found between IL4 rs2243250 and maternal atopy (OR = 1.41, P = 2.65 × 10–2). Conclusions Gene–gene interaction between IL13 rs20541, IL13 rs1800925, IL4 rs2243250 and ADRB2 rs1042713, and gene-environment interaction between IL4 rs2243250 and maternal atopy begin in prenatal stage to augment IgE production in Chinese Han children.

scholarly journals Investigation of the β-pinene photooxidation by OH in the atmosphere simulation chamber SAPHIR

2016 ◽  
Author(s):  
Martin Kaminski ◽  
Hendrik Fuchs ◽  
Ismail-Hakki Acir ◽  
Birger Bohn ◽  
Theo Brauers ◽  
...  
Keyword(s):  
Degradation Mechanism ◽  
Degradation Process ◽  
Product Distribution ◽  
High Reactivity ◽  
Oxidation Products ◽  
Chemical Mechanism ◽  
Emission Rates ◽  
Photochemical Degradation ◽  
Atmosphere Simulation Chamber ◽  
Simulation Chamber

Abstract. Beside isoprene, monoterpenes are the non-methane volatile organic compounds (VOC) with the highest global emission rates. Due to their high reactivity towards OH, monoterpenes can dominate the radical chemistry of the atmosphere in forested areas. In the present study the photochemical degradation mechanism of β-pinene was investigated in the Jülich atmosphere simulation chamber SAPHIR. The focus of this study is on the OH budget in the degradation process. Therefore the SAPHIR chamber was equipped with instrumentation to measure radicals (OH, HO2, RO2), the total OH reactivity, important OH precursors (O3, HONO, HCHO), the parent VOC beta-pinene, its main oxidation products, acetone and nopinone, and photolysis frequencies. All experiments were carried out under low NOx conditions (≤ 2 ppb) and at atmospheric beta-pinene concentrations (≤ 5 ppb) with and without addition of ozone. For the investigation of the OH budget, the OH production and destruction rates were calculated from measured quantities. Within the limits of accuracy of the instruments, the OH budget was balanced in all β-pinene oxidation experiments. However, even though the OH budget was closed, simulation results from the Master Chemical Mechanism 3.2 showed that the OH production and destruction rates were underestimated by the model. The measured OH and HO2 concentrations were underestimated by up to a factor of two whereas the total OH reactivity was slightly overestimated because of the poor reproduction of the measured nopinone by the model by up to a factor of three. A new, theory-derived first-generation product distribution by Vereecken and Peeters was able to reproduce the measured nopinone time series and the total OH reactivity. Nevertheless the measured OH and HO2 concentrations remained underestimated by the numerical simulations. These observations together with the fact that the measured OH budget was closed suggest the existence of unaccounted sources of HO2.

Newly Developed Heat Resistant Magnesium Alloy by Thixomolding®

2005 ◽  
Vol 488-489 ◽  
pp. 287-290 ◽  
Author(s):  
Tadayoshi Tsukeda ◽  
Ken Saito ◽  
Mayumi Suzuki ◽  
Junichi Koike ◽  
Kouichi Maruyama
Keyword(s):  
Aluminum Alloy ◽  
Magnesium Alloy ◽  
Magnesium Alloys ◽  
Room Temperature ◽  
Elevated Temperatures ◽  
Die Casting ◽  
The Other ◽  
Heat Resistant ◽  
Higher Temperature ◽  
Better Than

We compared the newly developed heat resistant magnesium alloy with conventional ones by Thixomolding® and aluminum alloy by die casting. Tensile properties at elevated temperatures of AXEJ6310 were equal to those of ADC12. In particular, elongation tendency of AXEJ6310 at higher temperature was better than those of the other alloys. Creep resistance of AXEJ6310 was larger than that of AE42 by almost 3 orders and smaller than that of ADC12 by almost 2 orders of magnitude. Fatigue limits at room temperature and 423K of AXEJ6310 was superior among conventional magnesium alloys.

Oxidation of Some Titanium Alloys in Air at Elevated Temperatures

2008 ◽  
Vol 595-598 ◽  
pp. 967-974 ◽  
Author(s):  
E. Godlewska ◽  
M. Mitoraj ◽  
B. Jajko
Keyword(s):  
Thermal Cycling ◽  
Titanium Alloys ◽  
Constant Temperature ◽  
Cross Sections ◽  
Elevated Temperatures ◽  
Mixed Oxides ◽  
Oxidation Mechanism ◽  
Testing Procedure ◽  
Oxidation Products ◽  
Outward Diffusion

This paper presents comparative studies on the performance of two titanium alloys (Ti- 6Al-1Mn, Ti-45.9Al-8Nb) in an oxidizing atmosphere at 700 oC and 800 oC. Testing procedure comprised thermogravimetric measurements at a constant temperature and in thermal cycling conditions (1-h and 20-h cycles at constant temperature followed by rapid cooling). The overall duration of the cyclic oxidation tests was up to 1000 hours. The oxidized specimens were analyzed in terms of chemical composition, phase composition, and morphology (SEM/EDS, TEM/EDS, XRD). The extent and forms of alloy degradation were evaluated on the basis of microscopic observation of specimen fractures and cross-sections. Selected specimens were examined by means of XPS, SIMS and GDS. Oxidation mechanism of Ti-46Al-8Nb was assessed a two-stage oxidation method using oxygen-18 and oxygen-16. Apparently, the oxidation of this alloy proceeded in several stages. According to XPS, already after quite short reaction time, the specimens were covered with a very thin oxide film, mainly composed of aluminum oxide (corundum). A thicker layer of titanium dioxide (rutile) developed underneath. These two layers were typical of the oxidation products formed on this alloy, even when tested in thermal cycling conditions. In general, the scale had a complex multilayer structure but it was thin and adherent. Under the continuous layer of titania, there was a fine-grained zone composed of mixed oxides. The alloy/scale interface was marked with niobium-rich precipitates embedded in a titanium-rich matrix. There were some indications of secondary processes occurring under the initial continuous oxide layers (e.g. characteristic layout of pores or voids). Thickness of inner scale layers clearly increased according to parabolic kinetics, while that of the outer compact layer (mainly TiO2) changed only slightly. The distribution of oxygen isotopes across the scale/alloy interface indicated two-way diffusion of the reacting species – oxygen inward and metals outward diffusion. Silicon deposited on Ti-6Al-1Mn alloy positively affected scale adhesion and remarkably reduced alloy degradation rate.

Network Changes in Nitrile Rubber at Elevated Temperatures

1973 ◽  
Vol 46 (2) ◽  
pp. 483-503 ◽  
Author(s):  
T. C. P. Lee ◽  
S. H. Morrell
Keyword(s):  
Heat Resistance ◽  
Structural Changes ◽  
Elevated Temperatures ◽  
Essential Feature ◽  
Nitrile Rubber ◽  
Polymer Backbone ◽  
Thermal Changes ◽  
Effective Antioxidant ◽  
Cleavage Reactions ◽  
Crosslinking Reactions

Abstract The network analysis of the aged sulfur vulcanizates of nitrile rubber serves to re-emphasize the complexity of the structural changes which can occur at elevated temperatures. Three factors control the rate and degree of crosslinking in these systems. First there is the crosslink structure. An essential feature for heat resistance in sulfur compounds is that they should contain, as near as possible, 100 per cent monosulfide crosslinks. Systems which contain polysulfide crosslinks, and probably to a lesser extent disulfide crosslinks, are prone to purely thermal crosslink shortening or cleavage reactions. The physical effect of these thermal changes would be superimposed on the effects brought about by thermooxidative changes. Despite their thermal stability monosulfide crosslinks can oxidize and cleave, a process which will result in stress relaxation if the sample is held in tension or compression. Hence for truly inert systems one will have to turn to non-sulfur cure in conjunction with a suitable stabilizer. Because the results indicate that scission associated with chemistry at the monosulfide crosslink is reversible, this cleavage does not contribute to the change in modulus or hardening during aging. This brings in the second controlling factor. The degree and rate of hardening depends on the nature of the products of vulcanization, and also possibly on those species intermediate between crosslink and accelerator, the pendent accelerator groups. In acting as an antioxidant ZDMC is apparently oxidized to a new source of sulfur. The more heat resistant cadmate system contains no such products and also a minimum of pendent accelerator groups. This leads to the third factor—the added antioxidant. For its heat resistance the cadmate system relies on an antioxidant. It is this which stops crosslinking reactions through autooxidation of the polymer backbone. The efficiency with which the antioxidant (dioctyldiphenylamine) works suggests that there is a synergistic effect in operation, which in some way involves cadmium. Thus the best heat resistance will be obtained where the compound yields monosulfide crosslinks, an uncomplicated network structure, unreactive vulcanization products, and contains a highly effective antioxidant system. Many facets of the aging of nitrile rubber are still open to explanation. Not the least of these is why crosslinks formed during the aging of the TMTD/S vulcanizate, which, by reason of their reactivity to methyl iodide, are thought to be sulfidic, are not themselves oxidized in a manner similar to the original monosulfide crosslinks. Model compound studies would answer this and other questions.

scholarly journals Isolation and Structure Determination of Echinochrome A Oxidative Degradation Products

Molecules ◽  
2020 ◽  
Vol 25 (20) ◽  
pp. 4778
Author(s):  
Natalia P. Mishchenko ◽  
Elena A. Vasileva ◽  
Andrey V. Gerasimenko ◽  
Valeriya P. Grigorchuk ◽  
Pavel S. Dmitrenok ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Degradation Products ◽  
Lethal Dose ◽  
Oxidative Degradation ◽  
Degradation Process ◽  
Oxidation Products ◽  
Chemical Mechanism ◽  
Ionization Mass ◽  
Echinochrome A ◽  
Esi Ms

Echinochrome A (Ech A, 1) is one of the main pigments of several sea urchin species and is registered in the Russian pharmacopeia as an active drug substance (Histochrome®), used in the fields of cardiology and ophthalmology. In this study, Ech A degradation products formed during oxidation by O2 in air-equilibrated aqueous solutions were identified, isolated, and structurally characterized. An HPLC method coupled with diode-array detection (DAD) and mass spectrometry (MS) was developed and validated to monitor the Ech A degradation process and identify the appearing compounds. Five primary oxidation products were detected and their structures were proposed on the basis of high-resolution electrospray ionization mass spectrometry (HR-ESI-MS) as 7-ethyl-2,2,3,3,5,7,8-heptahydroxy-2,3-dihydro-1,4-naphthoquinone (2), 6-ethyl-5,7,8-trihydroxy-1,2,3,4-tetrahydronaphthalene-1,2,3,4-tetraone (3), 2,3-epoxy-7-ethyl-2,3-dihydro-2,3,5,6,8-pentahydroxy-1,4-naphthoquinone (4), 2,3,4,5,7-pentahydroxy-6-ethylinden-1-one (5), and 2,2,4,5,7-pentahydroxy-6-ethylindane-1,3-dione (6). Three novel oxidation products were isolated, and NMR and HR-ESI-MS methods were used to establish their structures as 4-ethyl-3,5,6-trihydroxy-2-oxalobenzoic acid (7), 4-ethyl-2-formyl-3,5,6-trihydroxybenzoic acid (8), and 4-ethyl-2,3,5-trihydroxybenzoic acid (9). The known compound 3-ethyl-2,5-dihydroxy-1,4-benzoquinone (10) was isolated along with products 7–9. Compound 7 turned out to be unstable; its anhydro derivative 11 was obtained in two crystal forms, the structure of which was elucidated using X-ray crystallography as 7-ethyl-5,6-dihydroxy-2,3-dioxo-2,3-dihydrobenzofuran-4-carboxylic acid and named echinolactone. The chemical mechanism of Ech A oxidative degradation is proposed. The in silico toxicity of Ech A and its degradation products 2 and 7–10 were predicted using the ProTox-II webserver. The predicted median lethal dose (LD50) value for product 2 was 221 mg/kg, and, for products 7–10, it appeared to be much lower (≥2000 mg/kg). For Ech A, the predicted toxicity and mutagenicity differed from our experimental data.

Identification of α-Tocopherol Oxidation Products in Triolein at Elevated Temperatures

2001 ◽  
Vol 49 (3) ◽  
pp. 1508-1511 ◽  
Author(s):  
Tom Verleyen ◽  
Roland Verhe ◽  
Andre Huyghebaert ◽  
Koen Dewettinck ◽  
Wim De Greyt
Keyword(s):  
Elevated Temperatures ◽  
Oxidation Products
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