Study and Field Application of Organic/inorganic Cross-lining Blocking Agent for High Temperature Reservoir

Author(s):  
Caili Dai ◽  
Qing You ◽  
Xuezhe Liu ◽  
Wenming Wu ◽  
Long He ◽  
...  
SPE Journal ◽  
2021 ◽  
pp. 1-11
Author(s):  
Igor Ivanishin ◽  
Hisham A. Nasr-El-Din ◽  
Dmitriy Solnyshkin ◽  
Artem Klyubin

Summary High-temperature (HT) deep carbonate reservoirs are typically drilled using barite (BaSO4) as a weighting material. Primary production in these tight reservoirs comes from the network of natural fractures, which are damaged by the invasion of mud filtrate during drilling operations. For this study, weighting material and drilling fluid were sampled at the same drillsite. X-ray diffraction (XRD) and X-ray fluorescence analyses confirmed the complex composition of the weighting material: 43.2 ± 3.8 wt% of BaSO4 and 47.8 ± 3.3 wt% of calcite (CaCO3); quartz and illite comprised the rest. The drilling fluid was used to form the filter cake in a high-pressure/high-temperature (HP/HT) filter-press apparatus at a temperature of 300°F and differential pressure of 500 psig. Compared with the weighting material, the filter cake contained less CaCO3, but more nondissolvable minerals, including quartz, illite, and kaolinite. This difference in mineral composition makes the filter cake more difficult to remove. Dissolution of laboratory-grade BaSO4, the field sample of the weighting material, and drilling-fluid filter cake were studied at 300°F and 1,000 to 1,050 psig using an autoclave equipped with a magnetic stirrer drive. Two independent techniques were used to investigate the dissolution process: analysis of the withdrawn-fluid samples using inductively coupled plasma-optical emission spectroscopy, and XRD analysis of the solid material left after the tests. The dissolution efficiency of commercial K5-diethylenetriaminepentaacetic acid (DTPA), two K4-ethylenediaminetetraacetic acid (EDTA), Na4-EDTA solutions, and two “barite dissolvers” of unknown composition was compared. K5-DTPA and K4-EDTA have similar efficiency in dissolving BaSO4 as a laboratory-grade chemical and a component of the calcite-containing weighting material. No pronounced dissolution-selectivity effect (i.e., preferential dissolution of CaCO3) was noted during the 6-hour dissolution tests with both solutions. Reported for the first time is the precipitation of barium carbonate (BaCO3) when a mixture of BaSO4 and CaCO3 is dissolved in DTPA or EDTA solutions. BaCO3 composes up to 30 wt% of the solid phase at the end of the 6-hour reaction, and can be dissolved during the field operations by 5 wt% hydrochloric acid. Being cheaper, K4-EDTA is the preferable stimulation fluid. Dilution of this chelate increases its dissolution efficiency. Compared with commonly recommended solutions of 0.5 to 0.6 M, a more dilute solution is suggested here for field application. The polymer breaker and K4-EDTA solution are incompatible; therefore, the damage should be removed in two stages if the polymer breaker is used.


2005 ◽  
Vol 19 (12) ◽  
pp. 571-579 ◽  
Author(s):  
TAKAO MORINARI

It is argued that in two-dimension duality connects the CP1 representation of the S = 1/2 antiferromagnetic Heisenberg model with the Schwinger model in which Dirac fermions are interact via a U(1) gauge field. Application of this duality to underdoped high-temperature superconductors suggests that the high-energy fermionic excitation at the Mott insulating parent compound turns out to be a low-lying excitation in the spin disordered regime. A picture for high-temperature superconductivity is proposed.


2019 ◽  
Author(s):  
Xiangjuan Meng ◽  
Zhaocai Pan ◽  
Defei Chen ◽  
Zhou Su ◽  
Peng Wang ◽  
...  

2007 ◽  
Author(s):  
Yizheng Zhu ◽  
Fabin Shen ◽  
Zhengyu Huang ◽  
Kristie L. Cooper ◽  
Gary R. Pickrell ◽  
...  

2009 ◽  
Author(s):  
Modesto Mercado ◽  
Juan Carlos Acuna ◽  
Julio Estuardo Vasquez ◽  
Carlos Caballero ◽  
J. Eduardo Soriano

2021 ◽  
Author(s):  
Céleste Odier ◽  
Margaux Kerdraon ◽  
Emie Lacombe ◽  
Eric Delamaide

Abstract In heavy oil reservoirs operated by steam injection, foam has a double benefit. By improving the steam sweep efficiency within the reservoir, foam increases oil recovery while reducing the amount of injected steam. However, in the field, this technology is not always very effective due to the fact that it is difficult to find foaming agents that can withstand temperatures above 200°C. Moreover, the agents that form stable foams at such temperatures are often insoluble at ambient temperature, and therefore difficult to solubilize in the field. Thus, a compromise between good solubility in surface conditions and high temperature foaming performances in the reservoir has to be found. In this study, we show that it is possible to boost chemicals that form foam at very high temperature with an additive to greatly improve their solubility at ambient temperature while maintaining their high foaming performance at high temperature. Two foaming agents of increasing degree of hydrophobicity (H and HH) were initially selected for this study. The first one shows high foaming performances in porous media and in a high-pressure cell at temperatures comprised in between 150 and 220°C. The second one, more hydrophobic, is particularly performant at temperatures comprised in between 220°C and at least 280°C. Using a robotic platform, the temperature at which the foaming solution for agents H and HH needs to be heated to be solubilized, was evaluated with an accuracy of 5°C in four brines (varying salinity and hardness). We found that the temperature at which both agents become soluble is above 60°C, still too high for a field application. In the second part of the study, these hydrophobic molecules were coupled to a pre-selected additive. The resulting mixtures were again qualified in terms of solubility and foaming performances. We show that by coupling these hydrophobic agents with an additive, we are able to maintain their excellent foaming performances while decreasing their solubilisation temperature down to room temperature. To the best of our knowledge, this is the first time that very high temperature foam stability assessment up to 280°C is combined to solubility measurements to design performant foaming solutions that will be easy to handle in the field for steam foam applications. Interestingly, we show that the hydrophobicity of agents that is required for high temperature foam generation can be balanced by a more hydrophilic agent without reducing their foaming performances.


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