高质量聚钒酸铵连续结晶技术:偏转管式挡板结晶器的结晶机理与模拟

Ting Jiang, Jin Wang, Yuhan Qin, Chao Hu, Yue Ma, Lin Yang, Xingjian Kong, Linsen Wei
{"title":"高质量聚钒酸铵连续结晶技术:偏转管式挡板结晶器的结晶机理与模拟","authors":"Ting Jiang, Jin Wang, Yuhan Qin, Chao Hu, Yue Ma, Lin Yang, Xingjian Kong, Linsen Wei","doi":"10.1002/cjce.25488","DOIUrl":null,"url":null,"abstract":"This study introduces a novel technology for continuous vanadium precipitation, aiming to resolve issues such as poor stack density, small particle size, and irregular morphology of ammonium polyvanadate in traditional intermittent processes. In this research, we optimized the process parameters for continuous vanadium precipitation and investigated the mechanism of continuous ammonium polyvanadate crystallization using the focused beam reflectometer measurement. Results showed that small, flaky ammonium polyvanadate particles initially formed between 0 and 12 min. These particles subsequently interlayered and aggregated, resulting in larger particles from 13 to 23 min. By 24 to 60 min, a dynamic equilibrium was reached in crystal growth, aggregation, de‐embedding, and fragmentation. Kinetic analyses demonstrated that increasing the reaction temperature shifted crystal growth from surface reaction control to diffusion control. At higher temperatures, explosive nucleation of ammonium polyvanadate, crystal fragmentation, and dissolution occurred. By integrating the crystallization mechanism, we produced dense ellipsoidal ammonium polyvanadate particles with a stacking density of 0.772 g/cm<jats:sup>3</jats:sup> and an average size of 107.04 μm under optimal conditions, achieving a vanadium precipitation rate exceeding 99.0%. Simulation results confirmed that the deflector tube baffle crystallizer enabled continuous crystallization of ammonium polyvanadate, ensuring an average residence time of over 10 min for particles of 50 and 100 μm, facilitating their growth to at least 100 μm. This research provides data and theoretical support for the industrial application of continuous vanadium precipitation.","PeriodicalId":501204,"journal":{"name":"The Canadian Journal of Chemical Engineering","volume":"25 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A technique for continuous crystallization of high‐quality ammonium polyvanadate: Crystallization mechanism and simulation of deflector tube baffle crystallizer\",\"authors\":\"Ting Jiang, Jin Wang, Yuhan Qin, Chao Hu, Yue Ma, Lin Yang, Xingjian Kong, Linsen Wei\",\"doi\":\"10.1002/cjce.25488\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study introduces a novel technology for continuous vanadium precipitation, aiming to resolve issues such as poor stack density, small particle size, and irregular morphology of ammonium polyvanadate in traditional intermittent processes. In this research, we optimized the process parameters for continuous vanadium precipitation and investigated the mechanism of continuous ammonium polyvanadate crystallization using the focused beam reflectometer measurement. Results showed that small, flaky ammonium polyvanadate particles initially formed between 0 and 12 min. These particles subsequently interlayered and aggregated, resulting in larger particles from 13 to 23 min. By 24 to 60 min, a dynamic equilibrium was reached in crystal growth, aggregation, de‐embedding, and fragmentation. Kinetic analyses demonstrated that increasing the reaction temperature shifted crystal growth from surface reaction control to diffusion control. At higher temperatures, explosive nucleation of ammonium polyvanadate, crystal fragmentation, and dissolution occurred. By integrating the crystallization mechanism, we produced dense ellipsoidal ammonium polyvanadate particles with a stacking density of 0.772 g/cm<jats:sup>3</jats:sup> and an average size of 107.04 μm under optimal conditions, achieving a vanadium precipitation rate exceeding 99.0%. Simulation results confirmed that the deflector tube baffle crystallizer enabled continuous crystallization of ammonium polyvanadate, ensuring an average residence time of over 10 min for particles of 50 and 100 μm, facilitating their growth to at least 100 μm. This research provides data and theoretical support for the industrial application of continuous vanadium precipitation.\",\"PeriodicalId\":501204,\"journal\":{\"name\":\"The Canadian Journal of Chemical Engineering\",\"volume\":\"25 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Canadian Journal of Chemical Engineering\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/cjce.25488\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Canadian Journal of Chemical Engineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cjce.25488","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

本研究介绍了一种新型的连续钒沉淀技术,旨在解决传统间歇工艺中聚钒酸铵堆积密度差、粒度小、形态不规则等问题。在这项研究中,我们优化了连续钒沉淀的工艺参数,并利用聚焦光束反射仪测量法研究了聚钒酸铵连续结晶的机理。结果表明,在 0 到 12 分钟之间,最初形成的是片状的聚钒酸铵小颗粒。这些颗粒随后交错聚集,在 13 至 23 分钟内形成较大的颗粒。到 24 至 60 分钟时,晶体生长、聚集、脱嵌和碎裂达到了动态平衡。动力学分析表明,提高反应温度会使晶体生长从表面反应控制转向扩散控制。在更高的温度下,聚钒酸铵发生爆炸成核、晶体破碎和溶解。通过整合结晶机理,我们在最佳条件下制备出堆积密度为 0.772 g/cm3 的致密椭圆形聚钒酸铵颗粒,平均尺寸为 107.04 μm,钒析出率超过 99.0%。模拟结果证实,偏转管折流板结晶器能使聚钒酸铵连续结晶,确保 50 微米和 100 微米颗粒的平均停留时间超过 10 分钟,促进其至少生长到 100 微米。这项研究为连续钒沉淀的工业应用提供了数据和理论支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A technique for continuous crystallization of high‐quality ammonium polyvanadate: Crystallization mechanism and simulation of deflector tube baffle crystallizer
This study introduces a novel technology for continuous vanadium precipitation, aiming to resolve issues such as poor stack density, small particle size, and irregular morphology of ammonium polyvanadate in traditional intermittent processes. In this research, we optimized the process parameters for continuous vanadium precipitation and investigated the mechanism of continuous ammonium polyvanadate crystallization using the focused beam reflectometer measurement. Results showed that small, flaky ammonium polyvanadate particles initially formed between 0 and 12 min. These particles subsequently interlayered and aggregated, resulting in larger particles from 13 to 23 min. By 24 to 60 min, a dynamic equilibrium was reached in crystal growth, aggregation, de‐embedding, and fragmentation. Kinetic analyses demonstrated that increasing the reaction temperature shifted crystal growth from surface reaction control to diffusion control. At higher temperatures, explosive nucleation of ammonium polyvanadate, crystal fragmentation, and dissolution occurred. By integrating the crystallization mechanism, we produced dense ellipsoidal ammonium polyvanadate particles with a stacking density of 0.772 g/cm3 and an average size of 107.04 μm under optimal conditions, achieving a vanadium precipitation rate exceeding 99.0%. Simulation results confirmed that the deflector tube baffle crystallizer enabled continuous crystallization of ammonium polyvanadate, ensuring an average residence time of over 10 min for particles of 50 and 100 μm, facilitating their growth to at least 100 μm. This research provides data and theoretical support for the industrial application of continuous vanadium precipitation.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信