Novel Measurement of Asphaltene Content in Oil Using Microfluidic Technology
Published: 04/13/2013
Novel Measurement of Asphaltene Content in Oil Using Microfluidic Technology
Published: 04/13/2013
We present a state-of-the-art microfluidic technique for measuring the asphaltene content in crude oil samples. The automated microfluidic system improves data quality, reduces turnaround time, and minimizes solvent-volume consumption compared with conventional wet-chemistry measurements. The method is based on conventional precipitation techniques, such as the ASTM D6560, in which n-heptane is used for precipitation. However, instead of using gravimetric techniques commonly utilized in conventional methods, we use a novel spectrophotometry method for quantifying the asphaltenes. The optical technique is based on the spectral difference of crude oil before and after precipitation of asphaltenes using the titrant. We show a strong linear correlation between the optical method and the wet-chemistry technique for a broad selection of samples. The sample set included more than 50 crude oils with asphaltene contents as high as 15 wt.-%.
The unique microfluidic platform developed for this study uses a 200 ¦ÌL sample loop to deliver the crude sample into a microfluidic chaotic mixer, where the sample is mixed with toluene. After dilution, we injected the sample into a 2.5-mm path-length flow cell, where a visible spectrum of the oil is recorded. To measure the spectrum of the maltenes, the sample is mixed with n-heptane in the microfluidic mixer at a predefined volume ratio. The mixture then flows into a reactor channel, where the aggregation process takes place and asphaltene molecules grow into large aggregates. After precipitation, the mixture is passed through a 200-nm-pore membrane, where asphaltenes are trapped and maltenes permeate through the membrane. The spectrum of maltenes is then measured using the 2.5-mm path-length flow cell and a UV-VIS spectrometer.
Using the microfluidic technique, a complete measurement takes only 40 minutes, a considerable improvement over conventional wet-chemistry techniques that require a minimum of 2 days. Furthermore, conventional wet-chemistry measurements are highly operator dependent. We show that, for our optical technique, the repeatability of measurement is better than ¡À0.1 wt.-%. The microfluidic measurements require only 200 ¦ÌL of sample and 40 mL of solvent, which reduces the environmental impact of measurement. Finally, the small footprint of the apparatus makes it highly desirable for wellsite and offshore applications.