实时石油产品掺假检测器的研制

Olabisi Olotu, S. Isehunwa, B. Asiru, Z. Elakhame
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引用次数: 0

摘要

石油产品掺假及其对安全、健康、环境和经济的影响是尼日利亚和许多发展中国家面临的挑战。而监管机构和一些终端用户常用的保证石油产品质量的技术既耗时又昂贵。因此,本研究旨在开发一种实时检测石油产品掺假的装置。收集了汽油、柴油和煤油样本;收集水、石脑油、酒精、纯润滑油和用过的润滑油以及高倾燃料油(HPFO)作为液体污染物,而锯末、灰分和细砂作为固体颗粒。在23-28°C(1°C区间)的温度下,将纯产物与液体污染物(95:5,…(5: 95 V/V)和颗粒(0、2、4、6、8、10 g)。对二元液体混合物的SG和IFT建立了新的混合规则,并与Kay混合规则进行了比较。开发了物理化学特性的数学模型,用于模拟围绕具有多个输入/输出引脚和称重传感器的微控制器设计和构建的仪表。纯液固二元混合物的SG和IFT分别为0.810 ~ 1.020、25.5 ~ 47.2 dynes/cm和0.820 ~ 1.080、26.3和50.2 dynes/cm。对于固体颗粒污染的产品,SG在0.860 ~ 0.990之间。与Kay模型的0.83和25.6相比,新的混合规则给出的SG和IFT系数分别为0.84和27.8。产品掺假量为20-30%(按体积计)和10-20%(按污染质量计),掺假样品显示为红色,纯样品显示为绿色,数字形式的SG数值与实际测量值相差在±0.01%以内。研制了一种石油产品掺假实时检测装置,适用于类似二元混合物的实时检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of a Real–Time Petroleum Products Aduteration Detector
Adulteration of petroleum products with the resultant safety, health, environmental and economic impact is a challenge in Nigeria and many developing countries. While the commonly used techniques by regulatory agencies and some end-users for quality assurance of petroleum products are time-consuming and expensive. This study was therefore designed to develop a device for real-time detection of petroleum products adulteration. Samples of petrol, diesel and kerosene were collected; samples of water, naphtha, alcohol, pure and used lubricating oil, and High Pour Fuel Oil (HPFO) were collected and used as liquid contaminants while saw dust, ash and fine sand were used as solid particulates. At temperatures between 23-28°C (1°C interval), binary mixtures were prepared using the pure products with liquid contaminants (95:5, ..,5: 95 V/V) and with particulates (0, 2, 4, 6, 8,10 g). New mixing rules were developed for the SG and IFT of the binary liquid mixtures and compared with Kay mixing rule. Developed mathematical models of the physical-chemical properties were used to simulate a meter designed and constructed around a microcontroller with multiple input/output pins and a load cell sensor. The SG and IFT of the pure liquid and solid binary mixtures ranged from 0.810 to 1.020, 25.5 to 47.2 dynes/cm and 0.820 to 1.080 and 26.3 and 50.2 dynes/cm respectively. For products contaminated with solid particulates, SG varied between 0.860 and 0.990. The new mixing rule gave coefficient of 0.84 and 27.8 for SG and IFT compared with 0.83 and 25.6 of Kay's model. Adulteration of products was detected at 20-30% by volume and 10-20% by mass of contamination, and displayed RED for adulterated samples, GREEN for pure samples and numerical values of SG in digital form which were within ±0.01 % of actual measurements. A device for real-time detection of adulteration in petroleum products was developed which can be adapted to real-time evaluation of similar binary mixtures.
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