Hasan Imran, BinSharfan Ibtisam I, Khan Rais Ahmad, Alsalme Ali
Environmental Research Laboratory, Department of Chemistry, Chandigarh University, Gharuan, Mohali, Punjab 140301, India.
Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Nanomaterials (Basel). 2020 Nov 30;10(12):2402. doi: 10.3390/nano10122402.
In the present study, mesoporous silica nanoparticles (MSNs) synthesized through sol-gel process and calcined at 600 °C were further surface functionalized by a copolymer chain of L-ascorbic acid (AS) and polyaniline (PAni) by in situ free radical oxidative polymerization reaction. The surface modification of MSNs by AS-g-PAni was confirmed by using various analytical techniques, namely FTIR, XRD, SEM-EDX, TEM and AFM. The composition of AS-g-PAni@MS was found to be composed of C (52.53%), N (20.30%), O (25.69%) and Si (1.49%), with 26.42 nm as the particle size. Further, it was applied for the adsorption of crystal violet (CV) dye under batch, as well as fixed bed method. RSM-BBD was taken into consideration, to optimize the various operational parameters effecting the adsorption through batch method. To explore maximum efficiency of the material, it was further subjected to adsorption of CV under fixed bed method, using the variable bed heights of 3.7, 5.4 and 8.1 cm. Based on high value of regression coefficient (R) and low value of RMSE given as (0.99, 0.02) for 3.7 cm, (0.99, 0.03), the breakthrough data were very well defined by the Thomas model, with optimum concurrence of stoichiometric adsorption capacity values. The external mass transfer equilibrium data were well fitted by the Langmuir model, with maximum monolayer adsorption capacity of 88.42 mg g at 303K, 92.51 mg g at 313 K, 107.41 mg g at 313 K and 113.25 mg g at 333 K. The uptake of CV by AS-g-PAni@MS was well defined by pseudo second order model with rate constant K = 0.003 L mg min for 50 and 0.003 L mg min for 60 mg L CV. The adsorption reaction was endothermic with enthalpy (ΔH) value of 3.62 KJ mol and highly efficient for treatment of CV-contaminated water for more the five consecutive cycles.
在本研究中,通过溶胶 - 凝胶法合成并在600℃煅烧的介孔二氧化硅纳米颗粒(MSNs),通过L - 抗坏血酸(AS)和聚苯胺(PAni)的共聚物链原位自由基氧化聚合反应进一步进行表面功能化。通过使用各种分析技术,即傅里叶变换红外光谱(FTIR)、X射线衍射(XRD)、扫描电子显微镜 - 能谱分析(SEM - EDX)、透射电子显微镜(TEM)和原子力显微镜(AFM),证实了AS - g - PAni对MSNs的表面改性。发现AS - g - PAni@MS的组成包含C(52.53%)、N(20.30%)、O(25.69%)和Si(1.49%),粒径为26.42 nm。此外,将其应用于分批法以及固定床法下结晶紫(CV)染料的吸附。考虑采用响应曲面法 - Box - Behnken设计(RSM - BBD)来优化通过分批法影响吸附的各种操作参数。为了探索该材料的最大效率,在固定床法下,使用3.7、5.4和8.1 cm的可变床高对其进行CV吸附。基于回归系数(R)的高值和均方根误差(RMSE)的低值,对于3.7 cm给出的值为(0.99,0.02),对于5.4 cm为(0.99,0.03),突破数据由托马斯模型很好地定义,化学计量吸附容量值具有最佳一致性。外部传质平衡数据由朗缪尔模型很好地拟合,在303K时最大单层吸附容量为88.42 mg/g,在313K时为92.51 mg/g,在323K时为107.41 mg/g,在333K时为113.25 mg/g。AS - g - PAni@MS对CV的吸附符合准二级模型,对于50 mg/L CV的速率常数K = 0.003 L/(mg·min),对于60 mg/L CV的速率常数K = 0.003 L/(mg·min)。吸附反应是吸热的,焓(ΔH)值为3.62 KJ/mol,并且对于连续五个以上循环处理CV污染水具有高效性。