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在无机堿激活基质中对铬液废物进行惰性化处理:浸出和 NMR 多核方法。

Chromium liquid waste inertization in an inorganic alkali activated matrix: leaching and NMR multinuclear approach.

机构信息

University of Modena and Reggio Emilia, Department of Engineering "Enzo Ferrari", Modena, Italy.

University of Modena and Reggio Emilia, Department of Engineering "Enzo Ferrari", Modena, Italy.

出版信息

J Hazard Mater. 2015 Apr 9;286:474-83. doi: 10.1016/j.jhazmat.2014.12.054. Epub 2015 Jan 5.

Abstract

A class of inorganic binders, also known as geopolymers, can be obtained by alkali activation of aluminosilicate powders at room temperature. The process is affected by many parameters (curing time, curing temperature, relative humidity etc.) and leads to a resistant matrix usable for inertization of hazardous waste. In this study an industrial liquid waste containing a high amount of chromium (≈ 2.3 wt%) in the form of metalorganic salts is inertized into a metakaolin based geopolymer matrix. One of the innovative aspects is the exploitation of the water contained in the waste for the geopolymerization process. This avoided any drying treatment, a common step in the management of liquid hazardous waste. The evolution of the process--from the precursor dissolution to the final geopolymer matrix hardening--of different geopolymers containing a waste amount ranging from 3 to 20%wt and their capability to inertize chromium cations were studied by: i) the leaching tests, according to the EN 12,457 regulation, at different curing times (15, 28, 90 and 540 days) monitoring releases of chromium ions (Cr(III) and Cr(VI)) and the cations constituting the aluminosilicate matrix (Na, Si, Al); ii) the humidity variation for different curing times (15 and 540 days); iii) SEM characterization at different curing times (28 and 540 days); iv) the trend of the solution conductivity and pH during the leaching test; v) the characterization of the short-range ordering in terms of TOT bonds (where T is Al or Si) by (29)Si and (27)Al solid state magic-angle spinning nuclear magnetic resonance (ss MAS NMR) for geopolymers containing high amounts of waste (10-20%wt). The results show the formation of a stable matrix after only 15 days independently on the waste amount introduced; the longer curing times increase the matrices stabilities and their ability to immobilize chromium cations. The maximum amount of waste that can be inertized is around 10 wt% after a curing time of 28 days.

摘要

一类无机粘结剂,也称为地聚合物,可以通过在室温下对硅铝酸盐粉末进行碱激发来获得。该过程受许多参数(固化时间、固化温度、相对湿度等)的影响,并导致一种可用作危险废物惰性化的耐基质。在这项研究中,一种含有大量铬(≈2.3wt%)的工业废液以金属有机盐的形式被惰性化为偏高岭土基地聚合物基质。创新之处之一是利用废水中所含的水进行地质聚合反应。这避免了任何干燥处理,而干燥处理是处理液态危险废物的常见步骤。不同地聚合物的反应过程——从前驱体溶解到最终地聚合物基质硬化——含有 3%至 20%wt 的废水量,以及它们将铬阳离子惰性化的能力,通过以下方式进行了研究:i)浸出试验,根据 EN 12,457 法规,在不同固化时间(15、28、90 和 540 天)下监测铬离子(Cr(III)和 Cr(VI))和构成硅铝酸盐基质的阳离子(Na、Si、Al)的释放;ii)不同固化时间下的湿度变化(15 和 540 天);iii)不同固化时间(28 和 540 天)的 SEM 特征;iv)浸出试验过程中溶液电导率和 pH 的趋势;v)在含有高含量废物(10-20%wt)的地聚合物中,用(29)Si 和(27)Al固态魔角旋转核磁共振(ssMAS NMR)来测定 TOT 键(其中 T 是 Al 或 Si)的短程有序度。结果表明,无论引入的废水量如何,仅在 15 天后即可形成稳定的基质;固化时间越长,基质的稳定性和固定铬阳离子的能力就越高。在 28 天的固化时间后,可惰性化的最大废物量约为 10wt%。

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