Field Validation of a Non-logging Alternative Method for the Prediction of the Location of Water-Cresting in Horizontal Wells for Water-Drive Reservoirs.

A previously reported method for a non-logging alternative method for the prediction of the location of water-cresting in horizontal wells for water-drive reservoirs is validated in a field test for the first time in this study. Using this method, the wellbore trajectory, variation in the reservoir permeability, and the pressure gradient data were used to calculate what is called the breakthrough coefficient for the different segments along the length of a set horizontal well with the largest calculated breakthrough coefficient corresponding to the most likely location of the actual water-cresting occurrence. This method was field-validated and found to be in good agreement with log testing for a group of seven wells in an oilfield in Northern China. Another calculated parameter derived from the breakthrough coefficient which is called the variation of the breakthrough coefficients that characterize the effect of the variation of water production along the length of the horizontal well due to the effect of the variation of the wellbore trajectory, permeability, and pressure gradient on the oil production is also introduced. This field validation found variation of the breakthrough coefficients to be weakly and inversely correlated to the oil production in application to a group of 27 wells in the same field.

Method of Predicting the Location of Water Cresting for Horizontal Wells in a Water-Drive Reservoir for Early Prevention.

A method of prediction of location of water cresting and characterizing its intensity in a horizontal well in a water-drive reservoir is introduced for the first time. A mechanistic model for water cresting derived from Darcy's equation incorporating the main parameters reported in the literature affecting water cresting-viscosity, well distance to the aquifer, wellbore pressure gradient, and reservoir heterogeneity-is introduced with two new characterizing parameters. First is a model-derived parameter, called the breakthrough coefficient, which is defined as the ratio of the average time of breakthrough to the time of breakthrough for a segment of the well, with the model-predicted location of water cresting corresponding to the well segment with the largest breakthrough coefficient. The second is the Cresting index, which is the ratio of the maximum breakthrough coefficient to the minimum breakthrough coefficient as a characterizing parameter, with a well with a higher cresting index corresponding to a faster breakthrough in a group of similar wells. This methodology was validated through a series of sophisticated experimental corefloods and found to predict 78% of the location of the water cresting accurately. The cresting index is found to be weakly correlated with the speed of breakthrough among similar wells.

Experimental study on factors affecting the end effect in gas viscosity measurement using capillary-tube viscometer.

Because of its simple principle and high adaptability to severe operational conditions, the capillary-tube viscometer has been widely used for viscosity measurement. However, difficulties in accurately correcting the end effect induced measurement deviation will result in great uncertainty for measurement results. In order to solve this problem, in this work, we studied factors affecting the end effect by conducting the high pressure nitrogen viscosity measurement at low flow velocity with an improved capillary-tube viscometer. The experimental results indicated that the influence of the end effect became less significant with the decrease in flow velocity (v) and tube inner diameter (d) and varied inversely with the length of tube (L). We defined the ratio of measured viscosity to standard viscosity obtained from the NIST database as the viscosity deviation coefficient (Ce). From the Ce vs v, Ce vs d, and Ce vs L curves, we have observed that there existed a threshold velocity (vthreshold), a threshold diameter (dthreshold), and a threshold length (Lthreshold) at which Ce got closer to 1.0. It suggested that under certain experimental conditions, the influence of the end effect on gas viscosity measurement became negligible. Based on that, we established end effect free capillary-tube viscometry and compared the nitrogen viscosity results measured by this method with the data provided by the NIST database. The results presented a good match with error within 1.2%. These insights will contribute to improving the accuracy of a capillary-tube viscometer especially under high pressure.

Nucleic acid affinity of clustered-charge anion exchange adsorbents: effects of ionic strength and ligand density.

In previous work we demonstrated the improved protein-binding capacity and selectivity of ion-exchange adsorbents displaying a "clustered" rather than random, distribution of surface charges. For example, anion-exchange adsorbents displaying 5 mM of positive charge in the form of 1 mM penta-argininamide show much higher affinity and capacity for alpha-lactalbumin than do adsorbents displaying the same 5 mM total charge in the form of single dispersed argininamide charges. We also found that clustered adsorbents selectively favor proteins with inherent charge clustering. In the present work, "clustered" penta-argininamide adsorbents showed DNA binding capacity comparable to that of conventional dispersed adsorbents with 10-100-fold higher ligand density. We also observed that at moderate ionic strength the DNA affinity of all adsorbents tested increased with salt while RNA affinity decreased, so that selectivity for DNA over RNA was enhanced as salt concentration increased.

Enhanced protein affinity and selectivity of clustered-charge anion-exchange adsorbents.

In this work, we examined the possibility of improving ion-exchange adsorbent performance by nanoscale structuring of ligands into clusters of fixed size rather than a random distribution of individual charges. The calcium-depleted form of the protein alpha-lactalbumin, which displays a cluster of acidic amino acid residues, showed enhanced adsorption affinity and capacity on clustered-charge pentalysinamide and pentaargininamide adsorbents as compared to single-charge lysinamide and argininamide adsorbents of matched total charge. Two differently charge-clustered mutants of rat microsomal cytochrome b(5), E11Q and E44Q, with the same total charge also were well differentiated by clustered-charge adsorbents. Thus, an organized rather than random distribution of charges may produce adsorbents with higher capacity and selectivity, especially for biomolecules with inherent charge clustering.

Water-elutability of nucleic acids from metal-chelate affinity adsorbents: enhancement by control of surface charge density.

Immobilized metal affinity chromatography (IMAC) is widely used for purification of proteins, especially "hexahistidine-tagged" recombinant proteins. We previously demonstrated the application of IMAC to selective capture of nucleic acids, including RNA, selectively-denatured genomic DNA, and PCR primers through interactions with purine bases exposed in single-stranded regions. We also found that the binding affinity of nucleic acids for IMAC adsorbents can be increased several-fold by addition of 20 volume% of neutral additives such as ethanol or DMSO. In the present work, it is demonstrated that bound nucleic acids can be effectively eluted with water instead of the usual imidazole-containing competitive eluants, when the surface density of negative charges is enhanced by operation at alkaline pH, or by deliberate metal-underloading of the anionic chelating ligands. With enhanced negative surface charge density, nucleic acid adsorption can be made strongly dependent on the presence of adsorption-promoting additives and/or repulsion-shielding salts, and removal of these induces elution. Complete water-elutability is demonstrated for baker's yeast RNA bound to 10% Cu(II)- underloaded IDA Chelating Sepharose in a binding buffer of 20 mM HEPES, 240 mM NaCl, pH 7. Water elutability will significantly enhance the utility of IMAC in nucleic acid separations.

Neutral additives enhance the metal-chelate affinity adsorption of nucleic acids: role of water activity.

Immobilized metal-chelate affinity chromatography has been widely used in the purification of proteins, and we have recently found that it can also be applied to purification of nucleic acids through interactions involving exposed bases, especially purines. Here we report that the inclusion of moderate quantities of neutral solutes in the buffer substantially enhances the binding affinity of nucleic acids for immobilized metal-chelate affinity adsorbents. Addition of 20% (v/v) of solutes such as ethanol, methanol, isopropanol, n-propanol, and dimethyl sulfoxide enhances the initial affinity of binding of total yeast RNA by 4.4-, 3.8-, 3.7-, 3.0-, and 2.8-fold, respectively for Cu(II)-iminodiacetic acid (IDA) agarose adsorbent, and the weaker adsorption by Cu(II)-nitrilotriacetic acid (NTA) agarose was even more strongly enhanced. The adsorption affinities of the smaller oligodeoxynucleotide molecules A20, G20, C20 and T20 also increase with the addition of ethanol, suggesting that the effect is not significantly mediated by conformational changes. Binding enhancement generally correlates with reduction of water activity by the various solutes, as predicted by several models of solution thermodynamics, consistent with an entropic contribution by displacement of waters from the metal-chelate. Interestingly, the enhancement was not seen with the proteins bovine serum albumin and lysozyme.