Nicolás Di Luozzo, Michael Schulz, Michel Boudard, Silvina Limandri, Gastón Garbarino, Marcelo Fontana
{"title":"钢材的扩散粘接,整个接头的微观结构均匀一致","authors":"Nicolás Di Luozzo, Michael Schulz, Michel Boudard, Silvina Limandri, Gastón Garbarino, Marcelo Fontana","doi":"10.1007/s10853-024-10343-x","DOIUrl":null,"url":null,"abstract":"<div><p>Cold-finished carbon steel bars were bonded by means of the transient liquid phase bonding (TLPB) process using amorphous metallic foils of the eutectic Fe-B composition as filler material. A homogeneous microstructure throughout the joint was obtained. Traces of borides in the middle of the joint were the only distinguishable microconstituent from the base metal due to the TLPB process. The B concentration profile across the joint was measured by neutron radiography and was found to be composed of a central sharp peak with a maximum concentration of 15.9 ppm B superimposed over a broad peak (base width of ≈ 5 mm) with a maximum concentration of 13.3 ppm B. Owing to this low range of B concentrations, boride precipitation was almost suppressed, and only a scarce number of borides were observed at the joint. The resulting boride structure was identified as Fe<sub>23</sub>B<sub>6</sub> by synchrotron microfocused X-ray diffraction, and its stabilization at room temperature is discussed. The bonded samples were subjected to a bend test, with a bending angle of 180°, and no cracks were observed. In tension tests, the bonded samples attained an ultimate tensile strength (UTS) of 434 MPa, an elongation of 32.3% and a reduction area <i>q</i> of 51.2%—78.6%, 165.6% and 75.4%, respectively, of the base metal. The fracture of the bonded samples occurred at the joint. It was determined that the decrease in UTS compared with that of the base metal was due to the recovery, recrystallization and grain growth that occurred during the TLPB thermal cycle. In addition, from fracture surface observation, it was found that the decrease in <i>q</i> in bonded samples was caused by the presence of traces of borides at the joint, which were the result of the liquid phase that solidified during the cooling stage.</p><h3>Graphical abstract</h3><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":645,"journal":{"name":"Journal of Materials Science","volume":"59 43","pages":"20400 - 20417"},"PeriodicalIF":3.5000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Diffusion bonding of steels with a homogeneous microstructure throughout the joint\",\"authors\":\"Nicolás Di Luozzo, Michael Schulz, Michel Boudard, Silvina Limandri, Gastón Garbarino, Marcelo Fontana\",\"doi\":\"10.1007/s10853-024-10343-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Cold-finished carbon steel bars were bonded by means of the transient liquid phase bonding (TLPB) process using amorphous metallic foils of the eutectic Fe-B composition as filler material. A homogeneous microstructure throughout the joint was obtained. Traces of borides in the middle of the joint were the only distinguishable microconstituent from the base metal due to the TLPB process. The B concentration profile across the joint was measured by neutron radiography and was found to be composed of a central sharp peak with a maximum concentration of 15.9 ppm B superimposed over a broad peak (base width of ≈ 5 mm) with a maximum concentration of 13.3 ppm B. Owing to this low range of B concentrations, boride precipitation was almost suppressed, and only a scarce number of borides were observed at the joint. The resulting boride structure was identified as Fe<sub>23</sub>B<sub>6</sub> by synchrotron microfocused X-ray diffraction, and its stabilization at room temperature is discussed. The bonded samples were subjected to a bend test, with a bending angle of 180°, and no cracks were observed. In tension tests, the bonded samples attained an ultimate tensile strength (UTS) of 434 MPa, an elongation of 32.3% and a reduction area <i>q</i> of 51.2%—78.6%, 165.6% and 75.4%, respectively, of the base metal. The fracture of the bonded samples occurred at the joint. It was determined that the decrease in UTS compared with that of the base metal was due to the recovery, recrystallization and grain growth that occurred during the TLPB thermal cycle. In addition, from fracture surface observation, it was found that the decrease in <i>q</i> in bonded samples was caused by the presence of traces of borides at the joint, which were the result of the liquid phase that solidified during the cooling stage.</p><h3>Graphical abstract</h3><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":645,\"journal\":{\"name\":\"Journal of Materials Science\",\"volume\":\"59 43\",\"pages\":\"20400 - 20417\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-11-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Materials Science\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10853-024-10343-x\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Science","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s10853-024-10343-x","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Diffusion bonding of steels with a homogeneous microstructure throughout the joint
Cold-finished carbon steel bars were bonded by means of the transient liquid phase bonding (TLPB) process using amorphous metallic foils of the eutectic Fe-B composition as filler material. A homogeneous microstructure throughout the joint was obtained. Traces of borides in the middle of the joint were the only distinguishable microconstituent from the base metal due to the TLPB process. The B concentration profile across the joint was measured by neutron radiography and was found to be composed of a central sharp peak with a maximum concentration of 15.9 ppm B superimposed over a broad peak (base width of ≈ 5 mm) with a maximum concentration of 13.3 ppm B. Owing to this low range of B concentrations, boride precipitation was almost suppressed, and only a scarce number of borides were observed at the joint. The resulting boride structure was identified as Fe23B6 by synchrotron microfocused X-ray diffraction, and its stabilization at room temperature is discussed. The bonded samples were subjected to a bend test, with a bending angle of 180°, and no cracks were observed. In tension tests, the bonded samples attained an ultimate tensile strength (UTS) of 434 MPa, an elongation of 32.3% and a reduction area q of 51.2%—78.6%, 165.6% and 75.4%, respectively, of the base metal. The fracture of the bonded samples occurred at the joint. It was determined that the decrease in UTS compared with that of the base metal was due to the recovery, recrystallization and grain growth that occurred during the TLPB thermal cycle. In addition, from fracture surface observation, it was found that the decrease in q in bonded samples was caused by the presence of traces of borides at the joint, which were the result of the liquid phase that solidified during the cooling stage.
期刊介绍:
The Journal of Materials Science publishes reviews, full-length papers, and short Communications recording original research results on, or techniques for studying the relationship between structure, properties, and uses of materials. The subjects are seen from international and interdisciplinary perspectives covering areas including metals, ceramics, glasses, polymers, electrical materials, composite materials, fibers, nanostructured materials, nanocomposites, and biological and biomedical materials. The Journal of Materials Science is now firmly established as the leading source of primary communication for scientists investigating the structure and properties of all engineering materials.