N. Shohoji, Fernando Almeida Costa Oliveira, J. Galindo, Jorge Cruz Fernandes, José Rodríguez, I. Cañadas, L. Guerra Rosa
{"title":"SF40太阳炉中未裂解氨(NH3)气体线流速度对高浓度氮化物𝛅-MoN和𝛆-Fe2N形成的影响","authors":"N. Shohoji, Fernando Almeida Costa Oliveira, J. Galindo, Jorge Cruz Fernandes, José Rodríguez, I. Cañadas, L. Guerra Rosa","doi":"10.5923/j.ijmc.20190901.01","DOIUrl":null,"url":null,"abstract":"Nitriding experiments for powder specimens of Mo and Fe were carried out using a solar furnace SF40 at PSA (Plataforma Solar de Almeria) in Tabernas (Spain) in uncracked ammonia NH3 gas (NH3 gas with suppressed extent of dissociation by flowing) aiming at determining the range of linear velocity v of NH3 gas flow to yield higher nitride phases, δ-MoN for Mo and e-Fe2N for Fe. Standard solar exposure duration at a specified reaction temperature T was set to be 60 min over range of v between 1.14 mm·s-1 and 11.4 mm·s-1. By X-ray diffraction (XRD) analysis, presence of δ-MoN was detected besides γ-Mo2N and metallic Mo for Mo powder specimen heated to 900 oC in NH3 gas flow at v = 1.14 mm·s-1 but XRD peaks identifiable as δ-MoN became indiscernible when v was increased to 11.4 mm·s-1. On the other hand, for Fe powder specimen exposed to NH3 gas flow at v = 1.14 mm·s-1 at T = 500 oC, remnant metallic α-Fe was detectable by XRD at the down-stream side of the specimen holder but no metallic α-Fe was detected at the up-stream side of the specimen holder suggesting that chemical activity a(N) of N atom in uncracked NH3 gas tended to decrease along the NH3 gas flow path on going from the up-stream side to the down-stream side.","PeriodicalId":217478,"journal":{"name":"International Journal of Materials and Chemistry","volume":"31 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Influence of Linear Flow Velocity of Uncracked Ammonia (NH3) Gas on Formation of Higher Nitrides, 𝛅-MoN and 𝛆-Fe2N, under Concentrated Solar Irradiation in the SF40 Solar Furnace at PSA\",\"authors\":\"N. Shohoji, Fernando Almeida Costa Oliveira, J. Galindo, Jorge Cruz Fernandes, José Rodríguez, I. Cañadas, L. Guerra Rosa\",\"doi\":\"10.5923/j.ijmc.20190901.01\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Nitriding experiments for powder specimens of Mo and Fe were carried out using a solar furnace SF40 at PSA (Plataforma Solar de Almeria) in Tabernas (Spain) in uncracked ammonia NH3 gas (NH3 gas with suppressed extent of dissociation by flowing) aiming at determining the range of linear velocity v of NH3 gas flow to yield higher nitride phases, δ-MoN for Mo and e-Fe2N for Fe. Standard solar exposure duration at a specified reaction temperature T was set to be 60 min over range of v between 1.14 mm·s-1 and 11.4 mm·s-1. By X-ray diffraction (XRD) analysis, presence of δ-MoN was detected besides γ-Mo2N and metallic Mo for Mo powder specimen heated to 900 oC in NH3 gas flow at v = 1.14 mm·s-1 but XRD peaks identifiable as δ-MoN became indiscernible when v was increased to 11.4 mm·s-1. On the other hand, for Fe powder specimen exposed to NH3 gas flow at v = 1.14 mm·s-1 at T = 500 oC, remnant metallic α-Fe was detectable by XRD at the down-stream side of the specimen holder but no metallic α-Fe was detected at the up-stream side of the specimen holder suggesting that chemical activity a(N) of N atom in uncracked NH3 gas tended to decrease along the NH3 gas flow path on going from the up-stream side to the down-stream side.\",\"PeriodicalId\":217478,\"journal\":{\"name\":\"International Journal of Materials and Chemistry\",\"volume\":\"31 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Materials and Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5923/j.ijmc.20190901.01\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Materials and Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5923/j.ijmc.20190901.01","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4
摘要
在西班牙塔伯纳斯(Tabernas)的PSA (Plataforma solar de Almeria),利用SF40太阳炉对Mo和Fe粉末试样进行了氮化实验,目的是确定NH3气体流动线速度v的范围,以产生更高的氮化相,Mo为δ-MoN, Fe为e-Fe2N。在规定的反应温度T下,标准太阳照射时间设定为60分钟,v范围为1.14 mm·s-1至11.4 mm·s-1。通过x射线衍射(XRD)分析,在NH3气体流中加热至900℃,v = 1.14 mm·s-1时,Mo粉末试样除存在γ-Mo2N和金属Mo外,还存在δ-MoN,但当v增加到11.4 mm·s-1时,δ-MoN的XRD峰无法识别。另一方面,铁粉试样暴露在NH3气体流在v = 1.14毫米·s - 1在T = 500 oC,残余金属α铁由XRD检测标本夹,但没有加在一侧的金属α铁检测标本夹在上游一侧的表明N原子的化学活动(N)无裂缝的NH3气体倾向于减少沿着NH3气体流动路径上从上游到供应。
Influence of Linear Flow Velocity of Uncracked Ammonia (NH3) Gas on Formation of Higher Nitrides, 𝛅-MoN and 𝛆-Fe2N, under Concentrated Solar Irradiation in the SF40 Solar Furnace at PSA
Nitriding experiments for powder specimens of Mo and Fe were carried out using a solar furnace SF40 at PSA (Plataforma Solar de Almeria) in Tabernas (Spain) in uncracked ammonia NH3 gas (NH3 gas with suppressed extent of dissociation by flowing) aiming at determining the range of linear velocity v of NH3 gas flow to yield higher nitride phases, δ-MoN for Mo and e-Fe2N for Fe. Standard solar exposure duration at a specified reaction temperature T was set to be 60 min over range of v between 1.14 mm·s-1 and 11.4 mm·s-1. By X-ray diffraction (XRD) analysis, presence of δ-MoN was detected besides γ-Mo2N and metallic Mo for Mo powder specimen heated to 900 oC in NH3 gas flow at v = 1.14 mm·s-1 but XRD peaks identifiable as δ-MoN became indiscernible when v was increased to 11.4 mm·s-1. On the other hand, for Fe powder specimen exposed to NH3 gas flow at v = 1.14 mm·s-1 at T = 500 oC, remnant metallic α-Fe was detectable by XRD at the down-stream side of the specimen holder but no metallic α-Fe was detected at the up-stream side of the specimen holder suggesting that chemical activity a(N) of N atom in uncracked NH3 gas tended to decrease along the NH3 gas flow path on going from the up-stream side to the down-stream side.