Silica-rich Sodalite Synthesis: The Effect of Variations in Ultrasound Treatment and Hydrothermal Temperature

S. Sriatun, Marta Chandra Anikke Putri, Hanifa Zakiyatul Urbach, A. Darmawan, W. Widayat, H. Susanto
{"title":"Silica-rich Sodalite Synthesis: The Effect of Variations in Ultrasound Treatment and Hydrothermal Temperature","authors":"S. Sriatun, Marta Chandra Anikke Putri, Hanifa Zakiyatul Urbach, A. Darmawan, W. Widayat, H. Susanto","doi":"10.14710/jksa.25.4.137-145","DOIUrl":null,"url":null,"abstract":"Silica-rich sodalite zeolite has been synthesized by ultrasound treatment and hydrothermal temperature variation. This study aimed to determine the effect of ultrasound treatment and hydrothermal temperature variations on the crystallinity, hydrophobicity, and structural properties of silica-rich sodalite zeolite. The synthesis was conducted by reacting a sodium aluminate and sodium silicate solution by varying Si/Al ratios of 20, 30, 40, 60, 80, and 90. The next step was to characterize the product. The product with the best crystallinity was used as a reference to determine the effect of ultrasound and hydrothermal temperature. The reaction gel was treated with and without ultrasound and hydrothermal using autoclave at 100, 150, and 200°C for 24 hours. The last step was the product characterization using XRD, FTIR, and GSA. The XRD showed similarity peaks at 2θ = 14.058°; 24.41°; 31.73°; 34.75°; 42.88°. The best crystallinity was silica-rich sodalite zeolite with a Si/Al ratio of 30. Meanwhile, silica-rich sodalite zeolite peaks were obtained at 2θ = 14.16°, 24.66°, 31.99°, 35.13°, and 43.39° by ultrasound treatment and hydrothermal temperature variation (100, 150, and 200°C). Ultrasound treatment revealed the presence of other peaks besides sodalite at 2θ = 19.05° and 27°, where these peaks were referred to as SAPO-56. In conclusion, the degree of crystallinity increased with increasing temperature, decreasing Si-OH/Si-O-Si showed increased hydrophobic properties. Increasing the hydrothermal temperature of 150 and 200°C with and without ultrasound treatment increased the surface area significantly to 114.137 m2/g and 160.717 m2/g, and the pore volume of sodalite with a Si/Al ratio of 30 to 0.318 cc/g and 0.274 cc/g.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jurnal Kimia Sains dan Aplikasi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14710/jksa.25.4.137-145","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Silica-rich sodalite zeolite has been synthesized by ultrasound treatment and hydrothermal temperature variation. This study aimed to determine the effect of ultrasound treatment and hydrothermal temperature variations on the crystallinity, hydrophobicity, and structural properties of silica-rich sodalite zeolite. The synthesis was conducted by reacting a sodium aluminate and sodium silicate solution by varying Si/Al ratios of 20, 30, 40, 60, 80, and 90. The next step was to characterize the product. The product with the best crystallinity was used as a reference to determine the effect of ultrasound and hydrothermal temperature. The reaction gel was treated with and without ultrasound and hydrothermal using autoclave at 100, 150, and 200°C for 24 hours. The last step was the product characterization using XRD, FTIR, and GSA. The XRD showed similarity peaks at 2θ = 14.058°; 24.41°; 31.73°; 34.75°; 42.88°. The best crystallinity was silica-rich sodalite zeolite with a Si/Al ratio of 30. Meanwhile, silica-rich sodalite zeolite peaks were obtained at 2θ = 14.16°, 24.66°, 31.99°, 35.13°, and 43.39° by ultrasound treatment and hydrothermal temperature variation (100, 150, and 200°C). Ultrasound treatment revealed the presence of other peaks besides sodalite at 2θ = 19.05° and 27°, where these peaks were referred to as SAPO-56. In conclusion, the degree of crystallinity increased with increasing temperature, decreasing Si-OH/Si-O-Si showed increased hydrophobic properties. Increasing the hydrothermal temperature of 150 and 200°C with and without ultrasound treatment increased the surface area significantly to 114.137 m2/g and 160.717 m2/g, and the pore volume of sodalite with a Si/Al ratio of 30 to 0.318 cc/g and 0.274 cc/g.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
超声处理和水热温度变化对富硅钠盐合成的影响
采用超声处理和水热变温法制备了富硅钠沸石。本研究旨在确定超声处理和水热温度变化对富硅钠沸石结晶度、疏水性和结构性质的影响。在硅铝比分别为20、30、40、60、80和90的铝酸钠和硅酸钠溶液中进行合成。下一步是对产品进行表征。以结晶度最佳的产物为参照,考察超声和水热温度对产物结晶度的影响。反应凝胶分别在100、150、200℃的高压灭菌器下进行超声和水热处理24小时。最后一步是用XRD, FTIR和GSA对产物进行表征。XRD在2θ = 14.058°处显示相似峰;24.41°;31.73°;34.75°;42.88°。结晶度最好的是硅铝比为30的富硅钠沸石。同时,通过超声处理和水热温度变化(100、150和200℃),在2θ = 14.16°、24.66°、31.99°、35.13°和43.39°处得到了富硅钠石沸石峰。超声检查发现,在2θ = 19.05°和27°处,除了钠石外,还存在其他峰,这些峰被称为SAPO-56。综上所述,随着温度的升高,结晶度增加,Si-OH/Si-O-Si降低,疏水性增强。当水热温度为150℃和200℃时,超声处理和不超声处理均显著提高了钠石的比表面积,分别达到114.137 m2/g和160.717 m2/g,硅铝比为30 ~ 0.318 cc/g和0.274 cc/g时,钠石的孔体积显著增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
36
审稿时长
17 weeks
期刊最新文献
Production of Biodiesel from Candlenut Seed Oil (Aleurites Moluccana Wild) Using a NaOH/CaO/Ca Catalyst with Microwave Heating Synthesis of Molecularly Imprinted Polymers with Magnetite Cores for Ibuprofen Adsorption Impact of Fermentation on Hyptolide and Phytochemical Composition of Hyptis pectinata (L.) Poit Effects of Temperature, Molecular Weight, and Non-Solvent Variation on the Physical Properties of PVDF Membranes Prepared through Immersion Precipitation Isolation of Phenolic Acids from Land Kale (Ipomoea reptans Poir) and Antioxidant Activity
×
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
现在去查看 取消
×
提示
确定
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
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
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