مشخصات پژوهش

صفحه نخست /Graphitic carbon ...
عنوان
Graphitic carbon nitride-based 3D printed mixed matrix membrane thin film as a novel adsorbent for estrogenic hormone extraction from aqueous samples
نوع پژوهش مقاله ارائه شده
کلیدواژه‌ها
3D printing, Estrogen hormones, Aqueous samples, Thin film microextraction, Digital light processing (DLP) 3D printing.
چکیده
Nowadays, despite numerous attempts to safeguard water quality, uncontrolled water contamination such as estrogens resulting from human activities has become an enormous worry for the general public and a critical environmental issue [1]. Consequently, controlling the concentration of these substances is necessary to prevent detrimental effects on both humans and the environment [2]. For this reason, a 3D printed mixed matrix membrane (MMM) thin film, as a novel adsorbent, was introduced for the extraction of two steroid hormones from wastewater and tap water samples prior to their determination by highperformance liquid chromatography (HPLC-UV). The designed adsorbent was fabricated as thin film utilizing a digital light processing (DLP) 3D printing technique. The proposed thin film was made of acrylate photo resin, graphitic carbon nitride (g-C3N4), and polyvinylpyrrolidone (PVP) and its application was investigated for thin film microextraction (TFME) of 17β-estradiol (E2) and estrone (E1). The morphology of the 3D printed films surface and its chemical changes were studied using field emission scanning electron microscope (FE-SEM) and attenuated total reflectance fourier transform infrared spectroscopy (ATR-FTIR), respectively. Surface wettability of the proposed MMM films was measured by water contact angle analysis (WCA) and its porosity was studied by N2 adsorption/desorption analysis. To attain optimal microextraction performance, optimization of both thin film composition and microextraction procedure was conducted, followed by a thorough evaluation of figures of merit under the optimized conditions. Limit of detection (LOD) and limit of quantitation (LOQ) were determined to be 1.5 µg L-1 and 5 µg L-1 for both E2 and E1, respectively. The linear dynamic range (LDR) for both compounds was 5 -150 µg L-1. The method’s repeatability was investigated on a single film for 6 extractions, as well as on 3 different films and relative standard deviation (RSD) (%) val
پژوهشگران حدیثه رضائی (نفر اول)، امیرعباس متین (نفر دوم)