Acceleration of Zeolite Crystallization: Current Status, Mechanisms, and Perspectives

材料科学 结晶 电流(流体) 加速度 沸石 纳米技术 化学工程 催化作用 热力学 有机化学 经典力学 物理 工程类 化学
作者
En‐Hui Yuan,Rui Han,Junyu Deng,Wenwu Zhou,Anning Zhou
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:16 (23): 29521-29546 被引量:6
标识
DOI:10.1021/acsami.4c01774
摘要

Zeolites are important classes of crystalline materials and possess well-defined channels and cages with molecular dimensions. They have been extensively employed as heterogeneous catalysts and gas adsorbents due to their relatively large specific surface areas, high pore volumes, compositional flexibility, definite acidity, and hydrothermal stability. The zeolite synthesis normally undergoes high-temperature hydrothermal treatments with a relatively long crystallization time, which exhibits low synthesis efficiency and high energy consumption. Various strategies, e.g., modulation of the synthesis gel compositions, employment of special silica/aluminum sources, addition of seeds, fluoride, hydroxyl (·OH) free radical initiators, and organic additives, regulation of the crystallization conditions, development of new approaches, etc., have been developed to overcome these obstacles. And, these achievements make prominent contributions to the topic of acceleration of the zeolite crystallization and promote the fundamental understanding of the zeolite formation mechanism. However, there is a lack of the comprehensive summary and analysis on them. Herein, we provide an overview of the recent achievements, highlight the significant progress in the past decades on the developments of novel and remarkable strategies to accelerate the crystallization of zeolites, and basically divide them into three main types, i.e., chemical methods, physical methods, and the derived new approaches. The principles/acceleration mechanisms, effectiveness, versatility, and degree of reality for the corresponding approaches are thoroughly discussed and summarized. Finally, the rational design of the prospective strategies for the fast synthesis of zeolites is commented on and envisioned. The information gathered here is expected to provide solid guidance for developing a more effective route to improve the zeolite crystallization and obtain the functional zeolite-based materials with more shortened durations and lowered cost and further promote their applications.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
orixero应助这可怎么办啊采纳,获得10
刚刚
1秒前
贤君完成签到,获得积分10
2秒前
tangtang完成签到,获得积分10
2秒前
Orange应助小金采纳,获得10
3秒前
大大怪z完成签到,获得积分20
3秒前
3秒前
Liao发布了新的文献求助10
4秒前
刘倩发布了新的文献求助10
5秒前
5秒前
软软发布了新的文献求助10
5秒前
缥缈千柳发布了新的文献求助10
6秒前
蜘蛛侠发布了新的文献求助10
6秒前
6秒前
kkt发布了新的文献求助10
7秒前
情怀应助孙涛采纳,获得10
8秒前
9秒前
喜悦乐巧发布了新的文献求助10
9秒前
9秒前
10秒前
11秒前
飞快的寻云完成签到,获得积分10
11秒前
eeeeee完成签到,获得积分20
11秒前
小蘑菇应助泉竹晓筱采纳,获得10
12秒前
shijiu完成签到,获得积分20
12秒前
脑洞疼应助想要毕业采纳,获得10
12秒前
高高的茹妖完成签到,获得积分10
13秒前
一年半太久只争朝夕完成签到,获得积分10
13秒前
缓慢翠芙发布了新的文献求助10
14秒前
接两块钱发布了新的文献求助10
15秒前
Mininine完成签到 ,获得积分10
15秒前
16秒前
zhaozihao发布了新的文献求助10
16秒前
小龙发布了新的文献求助10
16秒前
科研通AI6.2应助snowdream采纳,获得10
17秒前
冷静博超发布了新的文献求助10
18秒前
justin完成签到,获得积分10
18秒前
zxf完成签到,获得积分10
18秒前
失眠如松发布了新的文献求助10
19秒前
21秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Modern Epidemiology, Fourth Edition 5000
Digital Twins of Advanced Materials Processing 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6024707
求助须知:如何正确求助?哪些是违规求助? 7657935
关于积分的说明 16177086
捐赠科研通 5173098
什么是DOI,文献DOI怎么找? 2767934
邀请新用户注册赠送积分活动 1751347
关于科研通互助平台的介绍 1637555