The corrosion of an Fe-based alloy containing 15 wt pct Y in H2-H2S mixtures under 10-3 Pa S2 was studied at 600~800℃ in an attempt to find materials with improved sulphidation resistance with respect to pure Fe. The...The corrosion of an Fe-based alloy containing 15 wt pct Y in H2-H2S mixtures under 10-3 Pa S2 was studied at 600~800℃ in an attempt to find materials with improved sulphidation resistance with respect to pure Fe. The presence of Y has been shown to be beneflcial, but not sufficient to the level expected. In fact, the alloy is able to form at all tested temperatures an external FeS layer, beneath which a zone containing a mixture of the two sulphides is also present. Thus,Fe can still diffuse through this region to form the outer FeS layer with non-negligible rate. The corrosion rate of Fe is considerably reduced by the Y addition. but the alloy corrodes still much more rapidly than Y. The sulphidation kinetics is generally rather irregular for both the pure metals, while the corrosion rate of the alloy decreases with time and tends to become parabolic after an initial period of 12~17 h. The sulphidation behaviour of the alloys is discussed by taking into account the presence of an intermetallic compound Fe17Y2 and the limited solubility of Y in Fe展开更多
Controlled oxidation experiments were performed on Kovar alloy by changing oxidation atmosphere, temperature, and exposure time to produce films with different oxide type and thickness. The results indicated that sing...Controlled oxidation experiments were performed on Kovar alloy by changing oxidation atmosphere, temperature, and exposure time to produce films with different oxide type and thickness. The results indicated that single Fe3O4 and single FeO were respectively obtained when Kovar alloy was oxidized in N2-2.31%H2O-0.95%H2 at 500℃ and in N2-2.31%H2O-0.5%H2 at 1000℃, and all kinetic curves followed linear relation; mixed oxides of FeO and Fe3O4 formed when Kovar was oxidized in N2-2.31%H2O at 1000℃and parabolic kinetics were obeyed. Analysis of metallographic cross section of oxides indicated that oxygen diffusion inward through the oxide scale is responsible for intergranular oxide, which had formed beneath the oxide scales when the oxide products were mixed oxides of FeO and Fe3O4, and which did not occur when the oxide was single FeO or Fe3O4. The oxidation model was also established.展开更多
The oxidation kinetics,surface morphology and phase structure of oxide films grown on 25Cr20Ni alloy in air-H2O and H2-H2O atmospheres at 900 ℃ for 20 h were investigated.The anti-coking performance and resistance to...The oxidation kinetics,surface morphology and phase structure of oxide films grown on 25Cr20Ni alloy in air-H2O and H2-H2O atmospheres at 900 ℃ for 20 h were investigated.The anti-coking performance and resistance to carburization of the two oxide films were compared using 25Cr20Ni alloy tubes with an inner diameter of 10 mm and a length of 850 mm in a bench scale naphtha steam pyrolysis unit.The oxidation kinetics followed a parabolic law in an air-H2O atmosphere and a logarithm law in a H2-H2O atmosphere in the steady-state stage.The oxide film grown in the air-H2O atmosphere had cracks where the elements Fe and Ni were enriched and the un-cracked area was covered with octahedral-shaped MnCr2O4 spinels and Cr1.3Fe0.7O3 oxide clusters,while the oxide film grown in the H2-H2O atmosphere was intact and completely covered with dense standing blade MnCr2O4 spinels.In the pyrolysis tests,the anti-coking performance and resistance to carburization of the oxide film grown in the H2-H2O atmosphere were far better than that in the air-H2O atmosphere.The mass of coke formed in the oxide film grown in the H2-H2O atmosphere was less than 10％ of that in the air-H2O atmosphere.The Cr1.3Fe0.7O3 oxide clusters converted into Cr23C6 carbides and the cracks were filled with carbon in the oxide film grown in the air-H2O atmosphere after repeated coking and decoking tests,while the dense standing blade MnCr2O4 spinels remained unchanged in the oxide film grown in the H2-H2O atmosphere.The ethylene,propylene and butadiene yields in the pyrolysis tests were almost the same for the two oxide films.展开更多
The structure of Na_2H_2[H_2V_2W_(18)O_(62)]12H_2O has been determined by x-ray analysis.The crystals are trigonal,space group R3m,with cell parameters a=37.613(11),c=12.972(7)A,V=15901(13)A^3,and Z=9.The structure mo...The structure of Na_2H_2[H_2V_2W_(18)O_(62)]12H_2O has been determined by x-ray analysis.The crystals are trigonal,space group R3m,with cell parameters a=37.613(11),c=12.972(7)A,V=15901(13)A^3,and Z=9.The structure model was refined by full-matrix least square to R=0.065 for 1702 reflections with F>4σ(F). The existence of the[H_2V_2W_(18)O_(62)]^(4-)heteropolyanion in the crystals has been confirmed.It is composed of two VO_4 tetrahedra and eighteen WO_6 octahedra linked to gve the Dawson-type structure.展开更多
MoS2/γ－Al2O3 ceramic composite membrane is successfully synthesized by the sol-gel method based on the inorganic salt route. The aluminum hydrate sol derived from the inorganic salt Al(NO3)3, whose transparence and ...MoS2/γ－Al2O3 ceramic composite membrane is successfully synthesized by the sol-gel method based on the inorganic salt route. The aluminum hydrate sol derived from the inorganic salt Al(NO3)3, whose transparence and viscosity are 97% and 1.2 × 10-3 Pa. s, respectively, can be formed through adjusting the ratio of the peptizing agent H+ to Al3+ to 0.3. The aluminum hydrate gel at 110℃ is amorphous in structure and is heat-treated in air at 800℃ to form γ－Al2O3. The precursor derived from the mixture solution of ammonium molybdate, thioacetamide and a reducing agent, can be transformed into crystal MoS2 under reducing condition at 800℃. MoS2/γ－Al2O3 composite membrane is an organic whole and bps no gradation from MoS2 layer to γ－Al2O3 Iayer. The separation factor a H2/H2S through the MoS2/γ－Al2O3 composite membrane increase with rising temperature and a H2/H2S at 600℃ is 4.45 higher than the theoretical separation factor produced by the ideal Knudsen diffusion.展开更多
文摘The corrosion of an Fe-based alloy containing 15 wt pct Y in H2-H2S mixtures under 10-3 Pa S2 was studied at 600~800℃ in an attempt to find materials with improved sulphidation resistance with respect to pure Fe. The presence of Y has been shown to be beneflcial, but not sufficient to the level expected. In fact, the alloy is able to form at all tested temperatures an external FeS layer, beneath which a zone containing a mixture of the two sulphides is also present. Thus,Fe can still diffuse through this region to form the outer FeS layer with non-negligible rate. The corrosion rate of Fe is considerably reduced by the Y addition. but the alloy corrodes still much more rapidly than Y. The sulphidation kinetics is generally rather irregular for both the pure metals, while the corrosion rate of the alloy decreases with time and tends to become parabolic after an initial period of 12~17 h. The sulphidation behaviour of the alloys is discussed by taking into account the presence of an intermetallic compound Fe17Y2 and the limited solubility of Y in Fe
基金supported by the National Natural Science Foundation of China(No. 50671014).
文摘Controlled oxidation experiments were performed on Kovar alloy by changing oxidation atmosphere, temperature, and exposure time to produce films with different oxide type and thickness. The results indicated that single Fe3O4 and single FeO were respectively obtained when Kovar alloy was oxidized in N2-2.31%H2O-0.95%H2 at 500℃ and in N2-2.31%H2O-0.5%H2 at 1000℃, and all kinetic curves followed linear relation; mixed oxides of FeO and Fe3O4 formed when Kovar was oxidized in N2-2.31%H2O at 1000℃and parabolic kinetics were obeyed. Analysis of metallographic cross section of oxides indicated that oxygen diffusion inward through the oxide scale is responsible for intergranular oxide, which had formed beneath the oxide scales when the oxide products were mixed oxides of FeO and Fe3O4, and which did not occur when the oxide was single FeO or Fe3O4. The oxidation model was also established.
基金financially supported by the scientific research project of China Petroleum and Chemical Corporation(No.409075)
文摘The oxidation kinetics,surface morphology and phase structure of oxide films grown on 25Cr20Ni alloy in air-H2O and H2-H2O atmospheres at 900 ℃ for 20 h were investigated.The anti-coking performance and resistance to carburization of the two oxide films were compared using 25Cr20Ni alloy tubes with an inner diameter of 10 mm and a length of 850 mm in a bench scale naphtha steam pyrolysis unit.The oxidation kinetics followed a parabolic law in an air-H2O atmosphere and a logarithm law in a H2-H2O atmosphere in the steady-state stage.The oxide film grown in the air-H2O atmosphere had cracks where the elements Fe and Ni were enriched and the un-cracked area was covered with octahedral-shaped MnCr2O4 spinels and Cr1.3Fe0.7O3 oxide clusters,while the oxide film grown in the H2-H2O atmosphere was intact and completely covered with dense standing blade MnCr2O4 spinels.In the pyrolysis tests,the anti-coking performance and resistance to carburization of the oxide film grown in the H2-H2O atmosphere were far better than that in the air-H2O atmosphere.The mass of coke formed in the oxide film grown in the H2-H2O atmosphere was less than 10％ of that in the air-H2O atmosphere.The Cr1.3Fe0.7O3 oxide clusters converted into Cr23C6 carbides and the cracks were filled with carbon in the oxide film grown in the air-H2O atmosphere after repeated coking and decoking tests,while the dense standing blade MnCr2O4 spinels remained unchanged in the oxide film grown in the H2-H2O atmosphere.The ethylene,propylene and butadiene yields in the pyrolysis tests were almost the same for the two oxide films.
文摘The structure of Na_2H_2[H_2V_2W_(18)O_(62)]12H_2O has been determined by x-ray analysis.The crystals are trigonal,space group R3m,with cell parameters a=37.613(11),c=12.972(7)A,V=15901(13)A^3,and Z=9.The structure model was refined by full-matrix least square to R=0.065 for 1702 reflections with F>4σ(F). The existence of the[H_2V_2W_(18)O_(62)]^(4-)heteropolyanion in the crystals has been confirmed.It is composed of two VO_4 tetrahedra and eighteen WO_6 octahedra linked to gve the Dawson-type structure.
文摘MoS2/γ－Al2O3 ceramic composite membrane is successfully synthesized by the sol-gel method based on the inorganic salt route. The aluminum hydrate sol derived from the inorganic salt Al(NO3)3, whose transparence and viscosity are 97% and 1.2 × 10-3 Pa. s, respectively, can be formed through adjusting the ratio of the peptizing agent H+ to Al3+ to 0.3. The aluminum hydrate gel at 110℃ is amorphous in structure and is heat-treated in air at 800℃ to form γ－Al2O3. The precursor derived from the mixture solution of ammonium molybdate, thioacetamide and a reducing agent, can be transformed into crystal MoS2 under reducing condition at 800℃. MoS2/γ－Al2O3 composite membrane is an organic whole and bps no gradation from MoS2 layer to γ－Al2O3 Iayer. The separation factor a H2/H2S through the MoS2/γ－Al2O3 composite membrane increase with rising temperature and a H2/H2S at 600℃ is 4.45 higher than the theoretical separation factor produced by the ideal Knudsen diffusion.
