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Enhancement mechanism of SO2 removal with calcium hydroxide in the presence of NO2
Jihui Gao,Guoqing Chen,Xiaolin Fu,Yijun Yin,Shaohua Wu,Yukun Qin 한국화학공학회 2012 Korean Journal of Chemical Engineering Vol.29 No.2
The enhancement mechanism of SO2 removal by the presence of NO2 under low temperature and humid conditions was studied in a fixed bed reactor system. The presence of NO2 in the flue gas can enhance SO2 removal. The interaction between SO2 and NO2 in gas phase could not explain the effect of NO2 on SO2 removal under lowtemperature and humid conditions. When Ca(NO3)2 and Ca(NO2)2 as additive were added on the surface of sorbent,the desulfurization activity of sorbent decreased. However, the sorbent pretreated by NO2 for a moment has higher SO2removal. The oxidization of SO32− to SO42− and the evolution of sorbent surface structure in the presence of NO2 can explain the enhancement of SO2 removal by the presence of NO2. HSO3− and SO3− reacted with NO2 to form sulfate,which can accelerate the hydrolysis of SO2. The reaction between NO2 and Ca(OH)2 can make the unreacted sorbet under the SO2 removal product exposed to the reactant gas.
Mechanism of SO_2 adsorption and desorption on commercial activated coke
Fei Sun,,Jihui Gao,Yuwen Zhu,,Yukun Qin 한국화학공학회 2011 Korean Journal of Chemical Engineering Vol.28 No.11
We used commercial activated coke (AC) as adsorbent and fixed-bed, FTIR, N_2 adsorption, ion chromatograph as research methods to study the SO2 removal mechanism in the presence of O_2 and H_2O and adsorbate (H_2SO_4)desorption mechanism by combined regeneration. The results showed that AC saturation sulfur retention (52.6 mg/g)in SO_2+O_2+H_2O atmosphere was 4.6 times as much as that (11.4mg/g) in SO_2+O_2 atmosphere and 5.0 times as much as that (10.6 mg/g) in SO_2+O_2 atmosphere at 90 ℃. O-2 and H_2O were necessary in AC desulfurization process. Reaction of SO_3 and H-2O (g) and condensation of sulfuric acid vapor were the dynamic of AC desulfurization process. Water vapor blowing in combined regeneration inhibited the reaction between H_2SO_4 and carbon, and consequently reduced the chemical lost of carbon. AC cumulative quality loss (53.6%) of five-times in C-R was still less than that (62.4%)of three-times in H-R. Water vapor blowing inhibited reactivation effect, as a result reducing the changes of AC pore structure and surface functional groups. Adsorbate H_2SO_4 generated in desulfurization evaporated to sulfuric acid vapor due to the high temperature in regeneration and was carried out by water vapor.
Yuwen Zhu,Jihui Gao,Fei Sun,Yukun Qin 한국화학공학회 2011 Korean Journal of Chemical Engineering Vol.28 No.12
Taixi anthracite was used as a precursor to prepare activated carbons (AC) for SO_2 adsorption from flue gas. In this work the activated carbons were prepared by physical activation with steam. Specifically, the effects of activation temperature and burn-off degree on the physico-chemical properties of the resulting AC samples were comparatively studied. The different types of pore volumes, pore size distributions and surface chemistries of the activated carbons on the SO_2 adsorption were also analyzed. The results show that the increasing burn-off leads to samples with continuous evolution of all types of pores except ultramicropore. The ultramicropore volume increases to a maximum of 0.169 cm^3/g at around 50% burn-off and then decreases for 850℃ activation. At higher activation temperature, the micropore volume decreases and the mesopore structure develops to a certain extent. For all the resulting AC samples,the quantities of the basic surface sites always appear much higher than the amount of the acidic sites. The activated carbon prepared with higher micropore volume, smaller median pore diameter and higher quantities of the basic surface sites represents better SO_2 sorption property.
Wei Qu,Yabin Zhou,Yundong Sun,Ming Fang,Han Yu,Wenjuan Li,Zhifang Liu,Jiping Zeng,Chunyan Chen,Chengjiang Gao,Jihui Jia 한국미생물학회 2011 The journal of microbiology Vol.49 No.2
Innate and adaptive immune responses are activated in humans when Helicobacter pylori invades the gastric mucosa. Nitric oxide (NO) and reactive nitrogen species are important immune effectors, which can exert their functions through oxidation and S-nitrosylation of proteins. S-nitrosoglutathione and sodium nitroprusside were used as NO donors and H. pylori cells were incubated with these compounds to analyze the inhibitory effect of NO. The suppressing effect of NO on H. pylori has been shown in vitro. Furthermore,the proteins modified by S-nitrosylation in H. pylori were identified through the biotin switch method in association with matrix-assisted laser desorption ionization/time-of-flight tandem mass spectrometry (MALDITOF-MS/MS). Five S-nitrosylated proteins identified were a chaperone and heat-shock protein (GroEL),alkyl hydroperoxide reductase (TsaA), urease alpha subunit (UreA), HP0721, and HP0129. Importantly,S-nitrosylation of TsaA and UreA were confirmed using purified recombinant proteins. Considering the importance of these enzymes in antioxidant defenses, adherence, and colonization, NO may exert its antibacterial actions by targeting enzymes through S-nitrosylation. Identification of protein S-nitrosylation may contribute to an understanding of the antibacterial actions of NO. Our findings provide an insight into potential targets for the development of novel therapeutic agents against H. pylori infection.
Oxidation of Zhundong subbituminous coal by Fe2+/H2O2 system under mild conditions
Shuai Chen,Wei Zhou,Mingjun Liu,Guangbo Zhao,Qingxi Cao,Bojun Zhao,Kaikai Kou,Jihui Gao 한국화학공학회 2020 Korean Journal of Chemical Engineering Vol.37 No.4
Oxidation of coal under mild conditions is effective not only to understand the macromolecular network structure of coal but also to produce useful chemicals, allowing more efficient application of coal resources. In this work, the mild oxidation of Zhundong subbituminous coal (ZS) by Fe2+/H2O2 system was carried out under various conditions, including [Fe2+]/[H2O2] molar ratio, temperature, H2O2 concentration and oxidation time. The liquid oxidation products were analyzed using gas chromatography/mass spectrometry (GC/MS), and the chemical structure changes were studied using Fourier transform infrared spectroscopy (FTIR). The results suggest that the oxidation efficiency of ZS with H2O2 is enhanced with the aid of Fe2+. The optimum conditions were determined to be [Fe2+]/[H2O2] molar ratio of 0.00453, H2O2 concentration of 3mol/L, 60 oC and 4 h according to the oxidation conversion rate. In total, 25 compounds were identified, which could be categorized as six group components. Most of them are valuedadded chemicals, and the content of benzene carboxylic acids is the highest among them, making up 29.99% of all group components in total relative content (TRC). -CH2- should be primary bridge connecting the aromatic rings, and alkylene chains linking three aromatic rings are abundant in ZS.