首页 > 最新文献

Fillers - Synthesis, Characterization and Industrial Application最新文献

英文 中文
Active Solders and Active Soldering 有源焊料和有源焊接
Pub Date : 2019-04-03 DOI: 10.5772/INTECHOPEN.82382
Shih-Ying Chang, Yan-Hua Huang, L. Tsao
Due to the relatively high stability of ceramic surfaces, ceramics, graphite, and alloys that easily form an oxide passivation layer by natural oxidation, such as aluminum alloys, titanium alloys, and magnesium alloys, are not wetted by common solders and brazing fillers. Moreover, in most applications, the brazing temperature is so high that it causes hot cracking or functional degradation of the difficult-to-wet materials. Active filler metals containing active elements have been developed, which can successfully join the nonwetting materials at low temperatures (<250°C) in air. The active elements, such as titanium, magnesium, and rare earth elements, in active solders play an important role in wettability and reactivity between filler metals and difficult-to-wet materials. Solders with active element content have been shown to provide excellent wettability. Hence, direct active soldering has been developed to simplify the manufacturing of difficult-to-wet material joints. A prac-tical understanding of the design and characterization of low melting point active solders and active soldering processes is elaborated in this chapter. The effects of active elements, active solder characteristics, mechanism of active soldering, active soldering techniques, and specific applications are introduced. The influence of the thermal and mechanical activation on the interfacial reactions between filler metals and difficult-to-wet materials during the active soldering process is also discussed.
由于陶瓷表面的稳定性比较高,容易通过自然氧化形成氧化钝化层的陶瓷、石墨和合金,如铝合金、钛合金、镁合金等,不被普通焊料和钎焊填料润湿。此外,在大多数应用中,钎焊温度太高,会导致难湿材料的热裂或功能退化。含有活性元素的活性填充金属在低温(<250℃)空气中可以成功地加入到非润湿材料中。活性焊料中的活性元素,如钛、镁和稀土元素,在填充金属和难湿材料之间的润湿性和反应性中起着重要作用。具有活性元素含量的焊料已被证明具有优异的润湿性。因此,直接主动焊接已经被开发出来,以简化难湿材料接头的制造。本章阐述了对低熔点活性焊料和活性焊接工艺的设计和表征的实际理解。介绍了活性元素的作用、活性焊料的特性、活性焊接的机理、活性焊接技术和具体应用。讨论了活性焊接过程中热活化和机械活化对钎料与难湿材料界面反应的影响。
{"title":"Active Solders and Active Soldering","authors":"Shih-Ying Chang, Yan-Hua Huang, L. Tsao","doi":"10.5772/INTECHOPEN.82382","DOIUrl":"https://doi.org/10.5772/INTECHOPEN.82382","url":null,"abstract":"Due to the relatively high stability of ceramic surfaces, ceramics, graphite, and alloys that easily form an oxide passivation layer by natural oxidation, such as aluminum alloys, titanium alloys, and magnesium alloys, are not wetted by common solders and brazing fillers. Moreover, in most applications, the brazing temperature is so high that it causes hot cracking or functional degradation of the difficult-to-wet materials. Active filler metals containing active elements have been developed, which can successfully join the nonwetting materials at low temperatures (<250°C) in air. The active elements, such as titanium, magnesium, and rare earth elements, in active solders play an important role in wettability and reactivity between filler metals and difficult-to-wet materials. Solders with active element content have been shown to provide excellent wettability. Hence, direct active soldering has been developed to simplify the manufacturing of difficult-to-wet material joints. A prac-tical understanding of the design and characterization of low melting point active solders and active soldering processes is elaborated in this chapter. The effects of active elements, active solder characteristics, mechanism of active soldering, active soldering techniques, and specific applications are introduced. The influence of the thermal and mechanical activation on the interfacial reactions between filler metals and difficult-to-wet materials during the active soldering process is also discussed.","PeriodicalId":310487,"journal":{"name":"Fillers - Synthesis, Characterization and Industrial Application","volume":"21 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"115016544","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Dynamic Mechanical Behaviour of Coir and Coconut Husk Particulate Reinforced Polymer Composites: The Effect of Exposure to Acidic Environment 椰壳和椰壳颗粒增强聚合物复合材料的动态力学行为:暴露于酸性环境的影响
Pub Date : 2019-04-03 DOI: 10.5772/INTECHOPEN.82889
D. Obada, Laminu Shettima Kuburi, D. Dodoo‐Arhin, Yongdan Hou, M. B. Balogun, M. Muhammad
This chapter describes an experimental investigation into the dynamic mechanical properties of coir and coconut husk particulate reinforced polymer composites which were prepared by the hot press method. The composite was immersed in a strongly acidic environment of pH 2.2 for a period of 14 and 28 days (14P and 28P). Values of storage modulus at different vibrational frequencies recorded for the polymers at low temperatures where the molecules are still tightly compressed and the region of first solid state transitions are: Control sample (CS ) —913.18, 984.18 and 979.94 MPa; 14P—505.54, 492.47 and 473.60 MPa and 28P—282.25, 298.70 and 285.36 MPa at 2, 5 and 10 Hz, respectively. While values of loss modulus at different vibrational frequencies are: CS—113.32, 109.43 and 107.62 MPa, 14P—92.92, 92.92 and 101.93 MPa and 28P—46.08, 45.61 and 45.18 MPa at 2, 5 and 10 Hz, respectively. Degradation of the mechanical properties was ascribed to the penetration and absorption that occurred between the acid solution and the composite constituents (matrix, filler, and fiber). It was found that frequency variation influenced the dynamic mechanical properties of the polymer composite at the points of measurement.
本章对热压法制备的椰壳颗粒增强聚合物复合材料的动态力学性能进行了实验研究。复合材料在pH 2.2的强酸环境中浸泡14天和28天(14P和28P)。不同振动频率下聚合物在低温下的存储模量值为:控制样品(CS) -913.18、984.18和979.94 MPa;在2、5和10 Hz时,分别为14P-505.54、492.47和473.60 MPa和28P-282.25、298.70和285.36 MPa。不同振动频率下的损耗模量分别为:CS-113.32、109.43、107.62 MPa, 14P-92.92、92.92、101.93 MPa, 28P-46.08、45.61、45.18 MPa,分别为2、5、10 Hz。机械性能的退化归因于酸溶液与复合成分(基体、填料和纤维)之间的渗透和吸收。结果表明,频率变化会影响聚合物复合材料在测量点的动态力学性能。
{"title":"Dynamic Mechanical Behaviour of Coir and Coconut Husk Particulate Reinforced Polymer Composites: The Effect of Exposure to Acidic Environment","authors":"D. Obada, Laminu Shettima Kuburi, D. Dodoo‐Arhin, Yongdan Hou, M. B. Balogun, M. Muhammad","doi":"10.5772/INTECHOPEN.82889","DOIUrl":"https://doi.org/10.5772/INTECHOPEN.82889","url":null,"abstract":"This chapter describes an experimental investigation into the dynamic mechanical properties of coir and coconut husk particulate reinforced polymer composites which were prepared by the hot press method. The composite was immersed in a strongly acidic environment of pH 2.2 for a period of 14 and 28 days (14P and 28P). Values of storage modulus at different vibrational frequencies recorded for the polymers at low temperatures where the molecules are still tightly compressed and the region of first solid state transitions are: Control sample (CS ) —913.18, 984.18 and 979.94 MPa; 14P—505.54, 492.47 and 473.60 MPa and 28P—282.25, 298.70 and 285.36 MPa at 2, 5 and 10 Hz, respectively. While values of loss modulus at different vibrational frequencies are: CS—113.32, 109.43 and 107.62 MPa, 14P—92.92, 92.92 and 101.93 MPa and 28P—46.08, 45.61 and 45.18 MPa at 2, 5 and 10 Hz, respectively. Degradation of the mechanical properties was ascribed to the penetration and absorption that occurred between the acid solution and the composite constituents (matrix, filler, and fiber). It was found that frequency variation influenced the dynamic mechanical properties of the polymer composite at the points of measurement.","PeriodicalId":310487,"journal":{"name":"Fillers - Synthesis, Characterization and Industrial Application","volume":"16 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2019-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131092221","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
The Effects of Novel Additives Used in PVA/Starch Biohybrid Films 新型添加剂对聚乙烯醇/淀粉生物杂化膜的影响
Pub Date : 2018-12-19 DOI: 10.5772/INTECHOPEN.81727
E. Karaogul, Ertuğrul Altuntaş, T. Salan, M. Alma
The main aim of this chapter is to indicate the importance of additives and modifications used for PVA/starch biohybrid films. The additives and modifications used to improve the mechanical, thermal, and morphological properties of films are plasticizers, cross-linkers, fillers, physical and chemical treatment, and natural materials as well as thermoplastic starch. Plasticizers are preferred for higher molecular dynamism because of flexibility of functional groups in PVA and starch. Their flexibility is considerably affected by carboxyl and hydroxyl groups of plasticizers. The use of cofunctional groups increases the plasticity, flexibility, and physicochemical and mechanical properties of films. Moreover, cross-linking modifications are also effective to enhance the properties of biofilms. These modifications improve the tensile strength, modulus of elasticity, water resistance, thermal resistance, swelling behavior, and antibacterial activity of films. Fillers are also used to enhance the properties of PVA/starch films. In this way, the properties such as gas barrier, mechanical stiffness, transparency and thermal stability of the filler-added films are improved. The chemical and physical modifications provide stronger hydrogen bonds in films due to increasing carboxyl groups. Thus, the physical, biological, and chemical properties of films are improved because of the changing molecular structure via esterification, etherification, hydrogen bonding, and oxidation. etherification, hydrogen bonding, and oxidation in their molecular structure.
本章的主要目的是指出用于PVA/淀粉生物杂化膜的添加剂和改性的重要性。增塑剂、交联剂、填料、物理和化学处理、天然材料以及热塑性淀粉是用来改善薄膜的机械、热学和形态性能的添加剂和改性剂。由于聚乙烯醇和淀粉中官能团的柔韧性,增塑剂具有较高的分子动力学。它们的柔韧性受增塑剂的羧基和羟基的影响很大。共官能团的使用增加了薄膜的可塑性、柔韧性以及物理化学和机械性能。此外,交联修饰也能有效地提高生物膜的性能。这些改性提高了薄膜的拉伸强度、弹性模量、耐水性、耐热性、膨胀性和抗菌活性。填料也用于增强PVA/淀粉薄膜的性能。从而提高了薄膜的气体阻隔性、机械刚度、透明度和热稳定性等性能。由于增加羧基,化学和物理修饰使薄膜中的氢键更强。因此,由于酯化、醚化、氢键和氧化作用改变了分子结构,薄膜的物理、生物和化学性能得到了改善。分子结构中的醚化、氢键和氧化。
{"title":"The Effects of Novel Additives Used in PVA/Starch Biohybrid Films","authors":"E. Karaogul, Ertuğrul Altuntaş, T. Salan, M. Alma","doi":"10.5772/INTECHOPEN.81727","DOIUrl":"https://doi.org/10.5772/INTECHOPEN.81727","url":null,"abstract":"The main aim of this chapter is to indicate the importance of additives and modifications used for PVA/starch biohybrid films. The additives and modifications used to improve the mechanical, thermal, and morphological properties of films are plasticizers, cross-linkers, fillers, physical and chemical treatment, and natural materials as well as thermoplastic starch. Plasticizers are preferred for higher molecular dynamism because of flexibility of functional groups in PVA and starch. Their flexibility is considerably affected by carboxyl and hydroxyl groups of plasticizers. The use of cofunctional groups increases the plasticity, flexibility, and physicochemical and mechanical properties of films. Moreover, cross-linking modifications are also effective to enhance the properties of biofilms. These modifications improve the tensile strength, modulus of elasticity, water resistance, thermal resistance, swelling behavior, and antibacterial activity of films. Fillers are also used to enhance the properties of PVA/starch films. In this way, the properties such as gas barrier, mechanical stiffness, transparency and thermal stability of the filler-added films are improved. The chemical and physical modifications provide stronger hydrogen bonds in films due to increasing carboxyl groups. Thus, the physical, biological, and chemical properties of films are improved because of the changing molecular structure via esterification, etherification, hydrogen bonding, and oxidation. etherification, hydrogen bonding, and oxidation in their molecular structure.","PeriodicalId":310487,"journal":{"name":"Fillers - Synthesis, Characterization and Industrial Application","volume":"60 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125883967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Carbothermal Synthesis of Spherical AlN Fillers 球形AlN填料的碳热合成
Pub Date : 2018-11-05 DOI: 10.5772/INTECHOPEN.81708
Qi Wang, Kexin Chen, Wenbin Cao
Micro-sized spherical AlN particles have presented great commercial potential as thermally conductive fillers for high-performance thermal interface materials, benefiting from their high thermal conductivity and good fluidity in the polymers. In this chapter, recent research progress in the carbothermal synthesis of spherical AlN fillers is highlighted. The influences of various synthetic parameters, includ-ing N 2 gas pressure, additive content, additive particle size, reaction temperature, reaction time, carbon content, and additive types, on the nitridation rate and the particle size and morphology of final AlN powders are summarized. More impor-tantly, the growth mechanism of micro-sized spherical AlN granules is deeply discussed as well.
由于其在聚合物中的高导热性和良好的流动性,微球形AlN颗粒作为高性能热界面材料的导热填料具有很大的商业潜力。本章重点介绍了近年来碳热合成球形AlN填料的研究进展。总结了n2气体压力、添加剂含量、添加剂粒度、反应温度、反应时间、碳含量、添加剂种类等合成参数对氮化速率和最终AlN粉体粒度及形貌的影响。更重要的是,深入探讨了微球形AlN颗粒的生长机理。
{"title":"Carbothermal Synthesis of Spherical AlN Fillers","authors":"Qi Wang, Kexin Chen, Wenbin Cao","doi":"10.5772/INTECHOPEN.81708","DOIUrl":"https://doi.org/10.5772/INTECHOPEN.81708","url":null,"abstract":"Micro-sized spherical AlN particles have presented great commercial potential as thermally conductive fillers for high-performance thermal interface materials, benefiting from their high thermal conductivity and good fluidity in the polymers. In this chapter, recent research progress in the carbothermal synthesis of spherical AlN fillers is highlighted. The influences of various synthetic parameters, includ-ing N 2 gas pressure, additive content, additive particle size, reaction temperature, reaction time, carbon content, and additive types, on the nitridation rate and the particle size and morphology of final AlN powders are summarized. More impor-tantly, the growth mechanism of micro-sized spherical AlN granules is deeply discussed as well.","PeriodicalId":310487,"journal":{"name":"Fillers - Synthesis, Characterization and Industrial Application","volume":"131 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2018-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121402181","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Fillers - Synthesis, Characterization and Industrial Application
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1