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100     Gas Wettability of Reservoir Rock Surfaces with Porous Media



                            dichloromethane extract liquor was dried with MgSO 4 and filtered. Finally,
                            the filtered liquor underwent vacuum distillation before it was precipitated in
                            ice ether (thevolume of ice ether is 10 times that of concentrated liquor). The
                            precipitate was filtered and placed in a vacuum over to dry to balance the
                            weight.

                            3.2.2.1.2   Synthesis of Fluorine Amphiphilic Polymeremulsion
                            80 mL deionized water was poured into a 250 mL three-necked flask, 0.2 g
                            NaHCO 3 and 0.5 g lauryl sodium sulfate (SDS) was added into it, and stirred
                            intensely until it dissolved. Then, 3 mL Tween-80 was injected and the stirring
                            speed increased to 300 r/min. It was stirred until it formed micelles, and the
                            macromolecule initiator was added while constantly stirring. Cupric bromide,
                            Ligand bipyridine, and fluorinated monomer were mixed and dissolved at
                            60 C, cooled in an ice-bath, and added to the above emulsified solution and

                            sheared as a uniform preemulsion with a shear emulsion mixer. The solution
                            was then moved to an oil-bath at 80 C and nitrogen was injected. Ascorbic

                            acid was added to start the reaction, and the reaction was stopped after
                            8 hours to obtain the emulsion.

                            3.2.2.2 EVALUATION OF PERFORMANCE OF FLUORINE AMPHIPHILIC
                            BLOCK POLYMER
                            3.2.2.2.1   Infrared Spectroscopic Analysis
                            Fluorine-containing methacrylate monomer tridecafluoro-octyl ester and
                            macro-initiator MPEG-Brwere were synthesized into amphiphilic block poly-
                            mer with different mole ratio, which was precipitated and then dried. The col-
                            umn was coated with KBr pellet. After the polymer is spotted and filmed, the
                            infrared spectrogram is conducted. At a scanning range of 4000B400 cm 21 ,
                            wave number precision was 0.01 cm 21  and resolution ratio was 1 cm 21 . The
                            results are shown in Figs. 3.7 and 3.8.

                            From Fig. 3.7, it can be seen that 2960 cm 21  presents expansion-feature
                            absorption peak of  CH 3 and  CH 2  . Peaks in 1460 and 730 cm 21  are
                            bending vibration peaks of methylene, and the peak at 1700 cm 21  is the
                            absorption peak of ester group. The ester group is displaced to 1740 and
                            1750 cm 21  in the figure, as the fluorine atom has a great influence on the
                            vibration absorption peak of adjacent groups, and it also illustrates that the
                            ester group has become a saturated ester group. The expansion vibration peak
                                                         21                                 21
                            of C F bond appears at 1110 cm  , and wave number of about 1200 cm  is
                            the characteristic absorption peak of C O C (ether bond). Additionally, the
                            graphs of the four kinds of polymers have no absorption peak of C 5 Cin
                            monomer at 1500B1700 cm   21 . It is concluded from the above results that
                            the monomer has reacted completely during the polymerization process and
                            the product presents the structure of a copolymer.

                            Furthermore, fluorine-containing methacrylate monomer tridecafluoro-octyl
                            ester (F08), Trifluorooctyl acrylate (F07), and dodecafluoroheptyl acrylate
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