Determination of Reaction Rate of In-situ Gelled Acids with Calcite Using the Rotating Disk Apparatus

Author(s):  
Ahmed I. Rabie ◽  
Ahmed Mohamed Gomaa ◽  
Hisham A. Nasr-El-Din
Keyword(s):  
SPE Journal ◽  
2011 ◽  
Vol 16 (04) ◽  
pp. 981-992 ◽  
Author(s):  
Ahmed I. Rabie ◽  
Ahmed M. Gomaa ◽  
Hisham A. Nasr-El-Din

Summary In-situ-gelled acids have been used extensively in matrix acidizing and acid fracturing for acid diversion and reducing the leakoff rate, respectively. A few studies investigated the rate of dissolution of calcite in polymer-based acids, yet none has addressed in detail the in-situ-gelled acids. Therefore, the aim of this work is to examine the mass transfer and the kinetics of the reaction of 5 wt% HCl in-situ-gelled acids with calcite and determine the effect of Fe crosslinker on the rate of calcite dissolution. The rate of reaction of 5 wt% HCl in-situ-gelled acid was measured using the rotating-disk apparatus. Rock samples of 1.5in. diameter and 1-in. length were used. The effect of temperature (100-250°F) and disk-rotational speed (100-1,800 rev/min) was investigated using Pink Desert limestone rock samples. Calcium concentration was measured in the collected samples and was used to determine the acid-reaction rate. Experimental results showed that the rate of calcite dissolution at 150°F was controlled mainly by the rate of mass transfer of the acid to the surface up to a disk rotational speed of 1,000 rev/min and by the rate of the surface reaction above this value. On the basis of the results obtained, the diffusion coefficient of 5 wt% HCl in in-situ-gelled acid at 150°F; the activation energy; and the reaction rate constant at 150, 200, and 250°F were determined for the first time. A power-law kinetic model was used to determine the kinetics parameters. The presence of Fe3+ crosslinker had a significant effect on the rate of dissolution in comparison with reactions with gelled acid (no crosslinker) at the same condition. The reaction rate decreased by a factor of 2.2 and by a factor of 1.4 when the reaction was conducted at 100 and 1,500 rev/min, respectively. A gel layer, formed on the surface, acted as a barrier between the acid and the rock, which reduced the rate of calcite dissolution.


1961 ◽  
Vol 38 (4) ◽  
pp. 545-562 ◽  
Author(s):  
L. Kecskés ◽  
F. Mutschler ◽  
I. Glós ◽  
E. Thán ◽  
I. Farkas ◽  
...  

ABSTRACT 1. An indirect paperchromatographic method is described for separating urinary oestrogens; this consists of the following steps: acidic hydrolysis, extraction with ether, dissociation of phenol-fractions with partition between the solvents. Previous purification of phenol fraction with the aid of paperchromatography. The elution of oestrogen containing fractions is followed by acetylation. Oestrogen acetate is isolated by re-chromatography. The chromatogram was developed after hydrolysis of the oestrogens 'in situ' on the paper. The quantity of oestrogens was determined indirectly, by means of an iron-reaction, after the elution of the iron content of the oestrogen spot, which was developed by the Jellinek-reaction. 2. The method described above is satisfactory for determining urinary oestrogen, 17β-oestradiol and oestriol, but could include 16-epioestriol and other oestrogenic metabolites. 3. The sensitivity of the method is 1.3–1.6 μg/24 hours. 4. The quantitative and qualitative determination of urinary oestrogens with the above mentioned method was performed in 50 pregnant and 9 non pregnant women, and also in 2 patients with granulosa cell tumour.


2020 ◽  
Author(s):  
Keishiro Yamashita ◽  
Kazuki Komatsu ◽  
Hiroyuki Kagi

An crystal-growth technique for single crystal x-ray structure analysis of high-pressure forms of hydrogen-bonded crystals is proposed. We used alcohol mixture (methanol: ethanol = 4:1 in volumetric ratio), which is a widely used pressure transmitting medium, inhibiting the nucleation and growth of unwanted crystals. In this paper, two kinds of single crystals which have not been obtained using a conventional experimental technique were obtained using this technique: ice VI at 1.99 GPa and MgCl<sub>2</sub>·7H<sub>2</sub>O at 2.50 GPa at room temperature. Here we first report the crystal structure of MgCl2·7H2O. This technique simultaneously meets the requirement of hydrostaticity for high-pressure experiments and has feasibility for further in-situ measurements.


2020 ◽  
Author(s):  
Luzia S. Germann ◽  
Sebastian T. Emmerling ◽  
Manuel Wilke ◽  
Robert E. Dinnebier ◽  
Mariarosa Moneghini ◽  
...  

Time-resolved mechanochemical cocrystallisation studies have so-far focused solely on neat and liquid-assisted grinding. Here, we report the monitoring of polymer-assisted grinding reactions using <i>in situ</i> X-ray powder diffraction, revealing that reaction rate is almost double compared to neat grinding and independent of the molecular weight and amount of used polymer additives.<br>


2020 ◽  
Author(s):  
Satoshi Morooka ◽  
Nobuo Nakada ◽  
Yuhki Tsukada ◽  
Wu Gong ◽  
Takuro Kawasaki ◽  
...  

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