New Formulation for Sandstone Acidizing That Eliminates Sand Production Problems in Oil and Gas Sandstone Reservoirs

2017 ◽  
Vol 139 (4) ◽  
Author(s):  
Mohamed Mahmoud
Keyword(s):  
Acetic Acid ◽  
Clay Minerals ◽  
Clay Mineral ◽  
Potassium Carbonate ◽  
Chelating Agents ◽  
Mineral Dissolution ◽  
Formation Damage ◽  
Dimensionless Number ◽  
Sand Production ◽  
Sandstone Rock

The sandstone rocks' integrity and consolidation may be highly affected by the type and the strength of the stimulation fluids. Strong acids such as HF/HCl impair the rock consolidation. The reduction in the sandstone rock consolidation will trigger the sand production. Sand causes erosion of downhole and surface equipment especially when it is produced with high gas flow rates. In this study, gentle stimulation fluids for sandstone that consists of chelating agents and catalyst were proposed. The chelating agents are diethylene triamine penta acetic acid (DTPA) and ethylene diamine tetra acetic acid (EDTA). This is the first time to introduce a catalyst (potassium carbonate) in sandstone acidizing. Potassium carbonate was found to work as a clay stabilizer and catalyst that enhances the dissolution of chlorite clay mineral in the sandstone rock. The objective of introducing the catalyst is to enhance the solubility of the insoluble minerals such as chlorite clay minerals. The change in the mechanical properties of sandstone rocks (Bandera and Berea) was evaluated. The possibility of the formation damage after using seawater-based chelating agents was investigated and compared to HF/HCl mud acid. Coreflooding experiments were conducted to evaluate the effect of these fluids on the rock integrity. Computed tomography (CT) scanner was used to assess the formation damage. Different models were used to predict the sand production possibility after the stimulation with chelating agent/catalyst, and this was compared to the HF/HCl mud acid. The results showed that the permeability of sandstone core increased after acidizing. The reduction in CT-number after acidizing confirmed that no formation damage occurred. Rock mechanics evaluation showed no major changes occurred in the rock moduli and no sand production was observed. The model results showed that using chelating gents to stimulate Berea (BR) and Bandera (BN) sandstone cores did not cause sand production. Applying the same models for cores stimulated by HF/HCl acids indicated high possibility of sand production. The addition of potassium carbonate to DTPA chelating agents enhanced the chlorite clay mineral dissolution based on the inductively coupled plasma (ICP) analysis. Potassium carbonate as a catalyst did not affect the sandstone integrity because it only enhanced the dissolution of chlorite clay minerals (selective dissolution) and did not affect the solubility of carbonate minerals which are the primary cementing materials in the sandstone cores. A new dimensionless number was developed that describes the relation between the number of pore volumes (PVs) contacted the rock and the radial distance from the wellbore.

scholarly journals Animal-sediment interactions: the effect of ingestion and excretion by worms on mineralogy

2004 ◽  
Vol 1 (1) ◽  
pp. 533-559 ◽  
Author(s):  
S. J. Needham ◽  
R. H. Worden ◽  
D. McIlroy
Keyword(s):  
Clay Minerals ◽  
Clay Mineral ◽  
Lumbricus Terrestris ◽  
Depositional Environments ◽  
Mineral Dissolution ◽  
Combined Processes ◽  
Accelerated Weathering ◽  
Low Grade ◽  
Fine Grained ◽  
Peak Broadening

Abstract. By controlled experiments that simulate marine depositional environments, it is shown that accelerated weathering and clay mineral authigenesis occur during the combined process of ingestion, digestion and excretion of fine-grained sediment by two species of annelid worms. Previously characterized synthetic mud was created using finely ground, low-grade metamorphic slate (temperature approximately 300°C) containing highly crystalline chlorite and muscovite. This was added to experiment and control tanks along with clean, wind-blown sand. Faecal casts were collected at regular intervals from the experimental tanks and, less frequently, from the control tanks. Over a period of many months the synthetic mud (slate) proved to be unchanged in the control tanks, but was significantly different in faecal casts from the experimental tanks that contained the worms Arenicola marina and Lumbricus terrestris. Chlorite was preferentially destroyed during digestion in the gut of A. marina. Both chlorite and muscovite underwent XRD peak broadening with a skew developing towards higher lattice spacing, characteristic of smectite formation. A neoformed Fe-Mg-rich clay mineral (possibly berthierine) and as-yet undefined clay minerals with very high d-spacing were detected in both A. marina and L. terrestris cast samples. We postulate that a combination of the low pH and bacteria-rich microenvironment in the guts of annelid worms may radically accelerate mineral dissolution and clay mineral precipitation processes during digestion. These results show that macrobiotic activity significantly accelerates weathering and mineral degradation as well as mineral authigenesis. The combined processes of sediment ingestion and digestion thus lead to early diagenetic growth of clay minerals in clastic sediments.

scholarly journals Animal-sediment interactions: the effect of ingestion and excretion by worms on mineralogy

2004 ◽  
Vol 1 (2) ◽  
pp. 113-121 ◽  
Author(s):  
S. J. Needham ◽  
R. H. Worden ◽  
D. McIlroy
Keyword(s):  
Clay Minerals ◽  
Clay Mineral ◽  
Lumbricus Terrestris ◽  
Depositional Environments ◽  
Mineral Dissolution ◽  
Combined Processes ◽  
Accelerated Weathering ◽  
Low Grade ◽  
Fine Grained ◽  
Peak Broadening

Abstract. By controlled experiments that simulate marine depositional environments, it is shown that accelerated weathering and clay mineral authigenesis occur during the combined process of ingestion, digestion and excretion of fine-grained sediment by two species of annelid worms. Previously characterized synthetic mud was created using finely ground, low-grade metamorphic slate (temperature approximately 300°C) containing highly crystalline chlorite and muscovite. This was added to experiment and control tanks along with clean, wind-blown sand. Faecal casts were collected at regular intervals from the experimental tanks and, less frequently, from the control tanks. Over a period of many months the synthetic mud (slate) proved to be unchanged in the control tanks, but was significantly different in faecal casts from the experimental tanks that contained the worms Arenicola marina and Lumbricus terrestris. Chlorite was preferentially destroyed during digestion in the gut of A. marina. Both chlorite and muscovite underwent XRD peak broadening with a skew developing towards higher lattice spacing, characteristic of smectite formation. A neoformed Fe-Mg-rich clay mineral (possibly berthierine) and as-yet undefined clay minerals with very high d-spacing were detected in both A. marina and L. terrestris cast samples. We postulate that a combination of the low pH and bacteria-rich microenvironment in the guts of annelid worms may radically accelerate mineral dissolution and clay mineral precipitation processes during digestion. These results show that macrobiotic activity significantly accelerates weathering and mineral degradation as well as mineral authigenesis. The combined processes of sediment ingestion and digestion thus lead to early diagenetic growth of clay minerals in clastic sediments.

DO WEAK OR STRONG ACIDS REMOVE CARBONATE CONTAMINATION FROM ANCIENT TOOTH ENAMEL MORE EFFECTIVELY? THE EFFECT OF ACID PRETREATMENT ON RADIOCARBON AND δ13C ANALYSES

Radiocarbon ◽  
2021 ◽  
pp. 1-18
Author(s):  
Rachel Wood ◽  
Andre Barros Curado Fleury ◽  
Stewart Fallon ◽  
Thi Mai Huong Nguyen ◽  
Anh Tuan Nguyen
Keyword(s):  
Acetic Acid ◽  
Chelating Agents ◽  
Tooth Enamel ◽  
Mineral Phase ◽  
Acid Pretreatment ◽  
Skeletal Material ◽  
Lower Porosity ◽  
Hot Environments ◽  
Strong Acids

ABSTRACT In hot environments, collagen, which is normally targeted when radiocarbon (14C) dating bone, rapidly degrades. With little other skeletal material suitable for 14C dating, it can be impossible to obtain dates directly on skeletal materials. A small amount of carbonate occurs in hydroxyapatite, the mineral phase of bone and tooth enamel, and has been used as an alternative to collagen. Unfortunately, the mineral phase is often heavily contaminated with exogenous carbonate causing 14C dates to underestimate the true age of a sample. Although tooth enamel, with its larger, more stable crystals and lower porosity, is likely to be more robust to diagenesis than bone, little work has been undertaken to investigate how exogenous carbonate can be effectively removed prior to 14C dating. Typically, acid is used to dissolve calcite and etch the surface of the enamel, but it is unclear which acid is most effective. This study repeats and extends earlier work using a wider range of samples and acids and chelating agents (hydrochloric, lactic, acetic and propionic acids, and EDTA). We find that weaker acids remove carbonate contaminants more effectively than stronger acids, and acetic acid is the most effective. However, accurate dates cannot always be obtained.

scholarly journals DFT Study of Electronic Structure and Optical Properties of Kaolinite, Muscovite, and Montmorillonite

Crystals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 618
Author(s):  
Layla Shafei ◽  
Puja Adhikari ◽  
Wai-Yim Ching
Keyword(s):  
Mechanical Properties ◽  
Optical Properties ◽  
Electronic Structure ◽  
Hydrogen Bonds ◽  
Clay Minerals ◽  
Clay Mineral ◽  
Bond Order ◽  
Deep Understanding ◽  
Pharmaceutical Applications ◽  
Structure Properties

Clay mineral materials have attracted attention due to their many properties and applications. The applications of clay minerals are closely linked to their structure and composition. In this paper, we studied the electronic structure properties of kaolinite, muscovite, and montmorillonite crystals, which are classified as clay minerals, by using DFT-based ab initio packages VASP and the OLCAO. The aim of this work is to have a deep understanding of clay mineral materials, including electronic structure, bond strength, mechanical properties, and optical properties. It is worth mentioning that understanding these properties may help continually result in new and innovative clay products in several applications, such as in pharmaceutical applications using kaolinite for their potential in cancer treatment, muscovite used as insulators in electrical appliances, and engineering applications that use montmorillonite as a sealant. In addition, our results show that the role played by hydrogen bonds in O-H bonds has an impact on the hydration in these crystals. Based on calculated total bond order density, it is concluded that kaolinite is slightly more cohesive than montmorillonite, which is consistent with the calculated mechanical properties.

scholarly journals Development of new novel constitutive model for deep reservoir sandstone rock for sand production application

2021 ◽  
Vol 1051 (1) ◽  
pp. 012093
Author(s):  
S K Subbiah ◽  
A Mohamad-Hussein ◽  
A Samsuri ◽  
M Z Jaafar ◽  
Y R Chen ◽  
...  
Keyword(s):  
Constitutive Model ◽  
Sand Production ◽  
New Novel ◽  
Sandstone Rock ◽  
Deep Reservoir

Volcanogenic clays in Jurassic and Cretaceous strata of England and the North Sea Basin

Clay Minerals ◽  
2000 ◽  
Vol 35 (1) ◽  
pp. 25-55 ◽  
Author(s):  
C. V. Jeans ◽  
D. S. Wray ◽  
R. J. Merriman ◽  
M. J. Fisher
Keyword(s):  
Clay Minerals ◽  
Clay Mineral ◽  
North Sea ◽  
Volcanic Ash ◽  
Hydrothermal Fluids ◽  
Mineral Deposits ◽  
The North ◽  
Clay Deposits ◽  
The North Sea ◽  
Thermal Doming

AbstractThe nature and origin of authigenic clay minerals and silicate cements in the Jurassic and Cretaceous sediments of England and the North Sea are discussed in relation to penecontemporaneous volcanism in and around the North Sea Basin. Evidence, including new REE data, suggests that the authigenic clay minerals represent the argillization of volcanic ash under varying diagenetic conditions, and that volcanic ash is a likely source for at least the early silicate cements in many sandstones. The nature and origin of smectite-rich, glauconite-rich, berthierine-rich and kaolin-rich volcanogenic clay mineral deposits are discussed. Two patterns of volcanogenic clay minerals facies are described. Pattern A is related to ash argillization in the non-marine and marine environments. Pattern B is developed by the argillization of ash concentrated in the sand and silt facies belts in the seas bordering ash-covered islands and massifs. It is associated with regression/ transgression cycles which may be related to thermal doming and associated volcanism, including the submarine release of hydrothermal fluids rich in Fe. The apparent paucity of volcanogenic clay deposits in the Jurasssic and Early Cretaceous sediments of the North Sea is discussed.

Adsorption of Organic Compounds on Refined Latvian Clay

2018 ◽  
Vol 788 ◽  
pp. 83-88
Author(s):  
Oskars Leščinskis ◽  
Ruta Švinka ◽  
Visvaldis Švinka
Keyword(s):  
Methyl Orange ◽  
Zeta Potential ◽  
Adsorption Capacity ◽  
Clay Minerals ◽  
Organic Compounds ◽  
Clay Mineral ◽  
Rhodamine B ◽  
Ph Value ◽  
Ftir Spectra ◽  
Ph Values

Clays are materials consisting of clay minerals and non-clay minerals. Clay mineral fraction is considered to be a nanofraction. Clay minerals can be used for water purification and treatment. Description and characterization of 3 different Latvian clay nanosized minerals from 3 different geological periods (clay Liepa from Devonian period, clay Vadakste from Triassic period and clay Apriki from Quaternary period) as well as their adsorption capacity concerning organic compounds such as methyl orange and rhodamine B are summarized. Nanosized clay mineral particles were obtained using sedimentation method. Particle size distribution, zeta potential and FTIR spectra is given. The adsorption tests of above mentioned organic compounds were carried out in water solutions at 3 different pH values. The adsorption values were determined by means of UV-spectrophotometric technique. Zeta potential values for clay minerals Apriki, Liepa and Vadakste are -40.9 mV, -49.6 mV and -43.0 mV, respectively. FTIR spectra show similar tendencies for all 3 clay minerals. The best adsorption capacity concerning methyl orange and rhodamine B were in solutions with a pH value of 2, whereas at neutral and alkaline pH values adsorption in 24 hours was not observed.

scholarly journals PHYSICO-CHEMICAL AND MINERALOGICAL PROPERTIES OF A CLAY MINERAL DEPOSIT IN GEHEKU, KOGI STATE, NIGERIA

2020 ◽  
Vol 45 (4) ◽  
Author(s):  
E.E.I. Irabor ◽  
A. K. Okunkpolor
Keyword(s):  
Thermal Shock ◽  
Clay Minerals ◽  
Clay Mineral ◽  
Thermal Shock Resistance ◽  
Mineral Deposit ◽  
Swelling Property ◽  
Working Temperature ◽  
Mineralogical Properties ◽  
Physico Chemical ◽  
Shock Resistance

The physico-chemical and mineralogical properties of a clay mineral deposit in Geheku, Kogi State, Nigeria were assessed. The results of the study revealed that the deposit consisted of phyllosilicate minerals- Illite, montmorillonite, kaolinite, halloysite, almandine; other minerals present were quartz and ramsdellite. The clay minerals exhibited good swelling property, medium plasticity, good thermal shock resistance and apparent porosity; it had refractoriness below 1200 oC. The properties of the clay reflected the combined properties of the constituent clay and non-clay minerals which recommends it for a variety of applications which requires the blend of property though the working temperature must be below 1200 oC. The clay mineral deposit colours were influenced by the minerals almadine and ramsdellite.

Clay mineral distribution related to rift activity, sea-level changes and paleoceanography in the Cretaceous of the Atlantic Ocean

Clay Minerals ◽  
1993 ◽  
Vol 28 (1) ◽  
pp. 61-84 ◽  
Author(s):  
M. Thiry ◽  
T. Jacquin
Keyword(s):  
Atlantic Ocean ◽  
Sea Level ◽  
Clay Minerals ◽  
Clay Mineral ◽  
Deep Sea ◽  
Depositional Environments ◽  
Sea Level Changes ◽  
Sea Floor ◽  
Deep Sea Sediments ◽  
Bottom Waters

AbstractThe distribution of clay minerals from the N and S Atlantic Cretaceous deep-sea sediments is related to rifting, sea-floor spreading, sea-level variations and paleoceanography. Four main clay mineral suites were identified: two are inherited and indicative of ocean geodynamics, whereas the others result from transformation and authigenesis and are diagnostic of Cretaceous oceanic depositional environments. Illite and chlorite, together with interstratified illite-smectite and smectite occur above the sea-floor basalts and illustrate the contribution of volcanoclastic materials of basaltic origin to the sediments. Kaolinite, with variable amounts of illite, chlorite, smectite and interstratified minerals, indicates detrital inputs from continents near the platform margins. Kaolinite decreases upward in the series due to open marine environments and basin deepening. It may increase in volume during specific time intervals corresponding to periods of falling sea-level during which overall facies regression and erosion of the surrounding platforms occurred. Smectite is the most abundant clay mineral in the Cretaceous deep-sea sediments. Smectite-rich deposits correlate with periods of relatively low sedimentation rates. As paleoweathering profiles and basal deposits at the bottom of Cretaceous transgressive formations are mostly kaolinitic, smectite cannot have been inherited from the continents. Smectite is therefore believed to have formed in the ocean by transformation and recrystallization of detrital materials during early diagenesis. Because of the slow rate of silicate reactions, transformation of clay minerals requires a long residence time of the particles at the water/sediment interface; this explains the relationships between the observed increases in smectite with long-term sea-level rises that tend to starve the basinal settings of sedimentation. Palygorskite, along with dolomite, is relatively common in the N and S Atlantic Cretaceous sediments. It is not detrital because correlative shelf deposits are devoid of palygorskite. Palygorskite is diagnostic of Mg-rich environments and is indicative of the warm and hypersaline bottom waters of the Cretaceous Atlantic ocean.

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