在水溶液中的石墨碳化物上有效吸附亚染料酸红色
1College of Environmental Science and Engineering, Dalian Maritime University, Dalian 116026, People's Republic of China.
ACS omega
|July 8, 2024
概括
胺基石墨碳化物 (M-g-C3N4) 显示了酸红染料的吸附能力创纪录,特别是在低pH下. 基于尿素的石墨碳化物 (U-g-C3N4) 是可回收的,这表明了广泛的工业潜力.
科学领域:
- 材料科学 材料科学 材料科学
- 环境化学环境化学
- 纳米技术纳米技术
背景情况:
- 石墨碳化物 (g-C3N4) 是消除污染物的有希望的材料.
- 废水中的染料污染给环境带来了重大挑战.
- 开发高效和可回收的吸附剂对于净化水非常重要.
研究的目的:
- 合成和比较两种类型的g-C3N4 (尿素基和胺基) 用于酸红 (ABR) 染料吸附.
- 为了研究溶液pH对吸附性能的影响.
- 评估吸附剂的吸附动力学,同热量,热力学和可回收性.
主要方法:
- 尿素和胺的直接化合成U-g-C3N4和M-g-C3N4.
- 吸附实验是在不同pH值的水溶液中进行的.
- 使用伪二次动力学和兰木尔异热模型分析吸附数据.
- 使用乙醇进行再生研究.
主要成果:
- 无论是U-g-C3N4还是M-g-C3N4,都显示了随着pH值的下降而增加的吸附能力.
- 在pH1.0下,M-g-C3N4实现了25635.64毫克g-1的ABR吸附能力,在pH1.0下达到创纪录的吸附能力.
- 吸附遵循伪二次动力学和兰木尔异热模型,表明自发和外热过程.
- 在与乙醇再生后,U-g-C3N4显示出出色的可回收性.
结论:
- 在ABR移除方面,M-g-C3N4表现出了卓越的性能,创造了新的基准.
- 吸附机制涉及质子化g-C3N4和阳离子ABR之间的静电吸引.
- U-g-C3N4的可回收性凸显了其在废水处理中可持续的工业应用的潜力.
相关概念视频
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
2.9K
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the...
2.9K
Electrophilic Aromatic Substitution: Nitration of Benzene
5.9K
The nitration of benzene is an example of an electrophilic aromatic substitution reaction. It involves the formation of a very powerful electrophile, the nitronium ion, which is linear in shape. The reaction occurs through the interaction of two strong acids, sulfuric and nitric acid.
5.9K
Preparation of Amines: Reductive Amination of Aldehydes and Ketones
2.8K
Carbonyl compounds and primary amines undergo reductive amination first to produce imines, followed by secondary amines in the same reaction mixture, using selective reducing agents like sodium cyanoborohydride or sodium triacetoxyborohydride. Reductive amination produces different degrees of substitution of amines depending on the starting amine substrate.
2.8K
Preparation of Amines: Reduction of Oximes and Nitro Compounds
3.5K
Oximes can be reduced to primary amines using catalytic hydrogenation, hydride reduction, or sodium metal reduction. The reduction of aliphatic and aromatic nitro compounds to primary amines takes place by either catalytic hydrogenation or by using active metals like Fe, Zn, and Sn in the presence of an acid.
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
3.5K
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
3.8K
Nitrous acid is a relatively weak and unstable acid prepared in situ by the reaction of sodium nitrite and cold, dilute hydrochloric acid. In an acidic solution, the nitrous acid undergoes protonation when it loses water to form a nitrosonium ion—an electrophile. Nitrous acid reacts with primary amines to give diazonium salts. The reaction is called diazotization of primary amines.
3.8K
Preparation of 1° Amines: Azide Synthesis
3.9K
Direct alkylation of ammonia produces polyalkylated amines, along with a quaternary ammonium salt. To exclusively prepare primary amines, the azide synthesis method can be used.
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
3.9K


