Simultaneous utilization of mine tailings and steel slag for producing geopolymers: Alkali-hydrothermal activation, workability, strength, and hydration mechanism

硅酸铝 材料科学 聚合物 尾矿 抗压强度 化学工程 沸石 热液循环 碱金属 硅酸铝钙 水泥 熔渣(焊接) 冶金 化学 复合材料 催化作用 有机化学 工程类
作者
Guofu Huang,Mianmian Wang,Qing Liu,Shasha Zhao,Haijian Liu,Fangfang Liu,Lijuan Feng,Jimei Song
出处
期刊:Construction and Building Materials [Elsevier]
卷期号:414: 135029-135029 被引量:24
标识
DOI:10.1016/j.conbuildmat.2024.135029
摘要

Utilization of aluminosilicate-rich solid waste via geopolymerization, such as mine tailings (MTs), possesses a dual advantage of reducing CO2 release from cement manufacturing and increasing tailings utilization. However, a major challenge for this technology is the low reactivity of MTs. In this study, an alkali-hydrothermal method at 200 °C was developed for MTs activation, and MTs were converted into an active alkaline aluminosilicate precursor that could play an alkaline activator-like role. Geopolymers were subsequently prepared from activated MTs and slag by simply adding water, and to improve the performance of geopolymers, steel slag (SS) was added as a supplementary alkali source. Results showed that the advantage of SS as a calcium-based alkaline material could be fully exerted in this system. The Ca(OH)2 phase derived from SS hydration increased the pH of the pore solution, on the one hand, and complexation reactions between Ca2+ ionized from Ca(OH)2 and Si and Al monomers dissolved from activated MTs might occur and generate calcium aluminosilicate hydrate gel, on the other hand. As a result, the addition of SS accelerated the hydration process, prompted the production of hydration products, and thus enhanced the strength of geopolymers. The 3-day and 28-day strengths of geopolymers achieved as high as 31.10 and 44.79 MPa, respectively, when SS content was kept at 10 wt%. In addition, SS-doped geopolymers had satisfactory soundness because the fast consumption of Ca2+ prevented the growth of Ca(OH)2 crystals and the resulting expansion effect.
最长约 10秒,即可获得该文献文件

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
Super完成签到,获得积分10
1秒前
哈呀3199完成签到 ,获得积分10
1秒前
晚风完成签到,获得积分10
2秒前
rice0601完成签到,获得积分10
3秒前
cxjie320完成签到,获得积分10
4秒前
牵着老虎晒月亮完成签到 ,获得积分10
5秒前
含糊的小蜜蜂完成签到,获得积分10
5秒前
酷波er应助晚风采纳,获得10
6秒前
6秒前
ccc完成签到,获得积分10
7秒前
我是老大应助woo采纳,获得10
7秒前
花痴的电灯泡完成签到,获得积分10
10秒前
RobinTest完成签到,获得积分10
11秒前
ykiiii完成签到,获得积分10
11秒前
unaqvq发布了新的文献求助10
11秒前
韩小小完成签到 ,获得积分10
13秒前
HAHAlyy完成签到,获得积分10
13秒前
平常莹芝完成签到,获得积分0
14秒前
小杰的逆袭人生完成签到,获得积分10
14秒前
Hello应助伊尔采纳,获得10
15秒前
zhizhi完成签到,获得积分10
16秒前
江南达尔贝完成签到 ,获得积分10
17秒前
18秒前
曾经碧蓉完成签到,获得积分10
19秒前
瓜兵是官爷完成签到,获得积分10
20秒前
午木完成签到,获得积分10
21秒前
21秒前
Biohacking完成签到,获得积分10
22秒前
冯宇完成签到,获得积分10
22秒前
1111完成签到,获得积分10
22秒前
Licifer完成签到,获得积分10
23秒前
李涛发布了新的文献求助10
23秒前
回来完成签到,获得积分10
23秒前
啦哈啦哈啦完成签到,获得积分10
23秒前
x_x完成签到,获得积分10
23秒前
24秒前
dawd12完成签到,获得积分10
24秒前
24秒前
mryun完成签到,获得积分10
24秒前
jh完成签到 ,获得积分10
25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
Handbook of pharmaceutical excipients, Ninth edition 5000
Digital Twins of Advanced Materials Processing 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
Polymorphism and polytypism in crystals 1000
Social Cognition: Understanding People and Events 800
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 6028597
求助须知:如何正确求助?哪些是违规求助? 7693300
关于积分的说明 16187008
捐赠科研通 5175826
什么是DOI,文献DOI怎么找? 2769758
邀请新用户注册赠送积分活动 1753143
关于科研通互助平台的介绍 1638943