Academic literature on the topic 'Water base overprint varnish'

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Journal articles on the topic "Water base overprint varnish"

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H., Abd El-Wahab*1 Gamal EL Meligi2.Mohamed Gomaa Hassaan3 &. A.Kazlauciunas4. "PREPARATION AND CHARACTERIZATION OF TERPOLYMERS NANO PARTICLES AND THEIR USE AS OVER PRINT VARNISHES FOR OFFSET INKS." GLOBAL JOURNAL OF ENGINEERING SCIENCE AND RESEARCHES 6, no. 3 (2019): 207–18. https://doi.org/10.5281/zenodo.2616906.

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New over print varnishes based on ethyl acrylate, 2-ethyl hexyl acrylate and methyl methacrylate (MMA) terpolymersnano emulsions were prepared. They give stable properties for a timeframe (half year strong) and low coagulum of ethyl acrylate ,2-ethyl hexyl acrylate and methylmethacrylate (MMA) terpolymer. Two surfactant systems were used as well as changing the monomers ratio in the presence of constant percent of initiator. The prepared polymers were investigated and confirmed IR spectroscopy, TGA, GPC molecular weight and TEM for  particle size (nm), also  by testing: solid content %, wet coagulum 100mesh, (g/l), viscosity (cP),pH,  hardness, adhesion. The prepared emulsions terpolymerspolymer were conducted to incorporate instandardformulationof water base overprint varnish and compared with trade mark emulsion polymer Johncryl 90. The prepared water base overprint varnish examined by viscosity, gloss, tackiness, adhesion to metal, adhesion to plastics and chemical resistance.
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Wang, Xiao Fang, Xian Fu Wei, and Pei Qing Huang. "Study on Performance of Adherence of Water-Base UV Varnish." Advanced Materials Research 174 (December 2010): 409–12. http://dx.doi.org/10.4028/www.scientific.net/amr.174.409.

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Adherence is very important for performance of water-base UV varnish and has directly effect on the quality of the coating and the following process. The samples of water-base UV varnish were prepared by different pre-polymers and monomers. The effect of volume shrinkage and wet-ability on the adhesion of water-base UV varnish is studied through a series of experiments. The results show that the volume shrinkage has apparent effect on the adhesion, the smaller the volume shrinkage is, the better adhesion of water-base UV varnish is; the volume shrinkage is increasing with the increasing of the numbers of the functional groups; wet-ability is necessary for the varnish which can adhere to the substrate and has no directly effect on the adherence.
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Wang, Xiao Fang, Xian Fu Wei, and Pei Qing Huang. "Effect of Photo-Initiator on Curing Rate of Water-Base UV Varnish." Advanced Materials Research 380 (November 2011): 112–16. http://dx.doi.org/10.4028/www.scientific.net/amr.380.112.

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The photo-initiator has a crucial role in the curing system of water-base UV varnish. The formulation of water-base UV varnish was designed and 4 different photo-initiators were chosen to make samples to study the effect of photo-initiator on the curing system of varnish. The curing results were tested and were compared. The results showed that the type and proportion of photo-initiator has great effects on the curing rate of water-base UV varnish, the best photo-initiator is 907. The mixed photo-initiators 907, TPO and ITX have been designed and the samples were prepared using the way of a formulation experiment. The result indicated that the curing rate of complex photo-initiator was lower than the curing rate of photo-initiator 907. The curing effect of the varnish samples is the best when the quantity of photo-initiator 907 is 6%。
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Wang, Dan Dan, Xian Fu Wei, and Bei Qing Huang. "Research on the Adhension of Water-Based Ink on UV Varnish." Applied Mechanics and Materials 469 (November 2013): 26–29. http://dx.doi.org/10.4028/www.scientific.net/amm.469.26.

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In order to enhance the adhension of ink, base ink was prepared with proper pigment and grinding resin, as well as dispersing agent, then compounded it and film-forming resin. The paper has studied the major factors, including grinding resin, film-forming resin and additives, which influenced the adhension of water-based ink on UV varnish. The results indicated that the content and the variety of grinding resin had a certain influence on the adhension of water-based ink. Besides, since the structure of film-forming resin is different, it has a significant effect on the adhension of water-based ink with the change of the variety of resin. Whats more, additives, which could decrease the surface tension of ink effectively and made the ink intend to adhere on UV varnish easily, is also an important factor that influences the adhension of the water-based ink on UV varnish.
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De Luca, Mariana P., Juçara R. Franca, Filipe Augusto F. F. Macedo, et al. "Propolis Varnish: Antimicrobial Properties against Cariogenic Bacteria, Cytotoxicity, and Sustained-Release Profile." BioMed Research International 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/348647.

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Varnishes are preparations that differ in the polymeric matrix and therapeutical agents. In dentistry they are used to prevent caries. In this study we developed a propolis varnish, considering propolis properties against cariogenic bacteria. To a chitosan polymeric base (CHV) was added ethanolic propolis extract in different concentrations: PV1 (5%), PV2 (10%), and PV3 (15%). Antimicrobial activity was carried out againstStreptococcus mutans(SM),Streptococcus sanguinis(SG),Streptococcus salivarius(SS), andLactobacillus casei(LC) through agar diffusion method. The three propolis concentrations incorporated were effective in inhibiting the growth of all microorganisms, but without significant difference between the zones of inhibition observed. Cytotoxicity assay was done by MTT method. Data were analyzed by one-way ANOVA and Bonferroni test. None of the varnishes were cytotoxic, keeping 80% of viable cells, while CHV allowed cellular proliferation (120%). Sustained-release test was carried out by applying 40 μL of each varnish in the buccal surface of bovine teeth and kept in an ethanol/water solution removed in regular times. According to the “independent model approach,” the release profiles were distinct from each varnish and the most prolonged was PV3 (8 weeks). Varnish formulations had satisfactory antimicrobial activity against cariogenic bacteria and have a low cytotoxicity (<50%).
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Hrytsak, S. A., M. M. Ilkiv, V. R. Solonynka, Ya M. Bilyy, and B.-D. R. Gorak. "Research of the influence of quantitative content and type of hardener on the properties of water-emulsion varnishes of domestic production." Forestry, Forest, Paper and Woodworking Industry 46 (December 30, 2020): 82–89. http://dx.doi.org/10.36930/42204609.

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In recent years, water-soluble, water-emulsion and other relatively environmentally friendly materials have become widespread. In the manufacture of products in enterprises, the consumer is less interested in the type of finishing material, but there is a direction associated with the finishing processes that directly affect the final consumer. This direction is the equipment of wooden floor coverings. Since most of these floor coverings are installed without finishing, they need further finishing directly on the installation site. Therefore, in order to reduce the negative impact on the health of the consumer, finishing works are carried out with acrylic, acrylic-polyurethane or polyurethane water-emulsion materials. Since the coatings formed by acrylic emulsions have low resistance to abrasion and water, they are mostly used for the manufacture of primers. Polyurethane or polyurethane-acrylic emulsions are used to make high-quality varnishes. It should be noted that in order to ensure high performance indicators, preference is given to two-component compositions which include a varnish-base and an isocyanate hardener. Most of the raw materials for manufacturing of two-component water-emulsion polyurethane varnishes are imported and quite expensive. Therefore, the urgent task is to establish the optimal ratio between its components. This is necessary to obtain cost-effective materials that will form h
 In recent years, water-soluble, water-emulsion and other relatively environmentally friendly materials have become widespread. In the manufacture of products in enterprises, the consumer is less interested in the type of finishing material, but there is a direction associated with the finishing processes that directly affect the final consumer. This direction is the equipment of wooden floor coverings. Since most of these floor coverings are installed without finishing, they need further finishing directly on the installation site. Therefore, in order to reduce the negative impact on the health of the consumer, finishing works are carried out with acrylic, acrylic-polyurethane or polyurethane water-emulsion materials. Since the coatings formed by acrylic emulsions have low resistance to abrasion and water, they are mostly used for the manufacture of primers. Polyurethane or polyurethane-acrylic emulsions are used to make high-quality varnishes. It should be noted that in order to ensure high performance indicators, preference is given to two-component compositions which include a varnish-base and an isocyanate hardener. Most of the raw materials for manufacturing of two-component water-emulsion polyurethane varnishes are imported and quite expensive. Therefore, the urgent task is to establish the optimal ratio between its components. This is necessary to obtain cost-effective materials that will form high-quality coatings. So, this paper presents the results of the first stage of research on the properties of two-component water-emulsion polyurethane varnishes, which are being developed by one of the Ukrainian enterprise. The results of research of hardness of the protective and decorative coverings formed by varnishes on the basis of polyurethane emulsions with addition of isocyanate hardeners are resulted. The dependence of technological parameters of varnish application on the type and quantitative content of isocyanate hardener is described.
 igh-quality coatings. So, this paper presents the results of the first stage of research on the properties of two-component water-emulsion polyurethane varnishes, which are being developed by one of the Ukrainian enterprise. The results of research of hardness of the protective and decorative coverings formed by varnishes on the basis of polyurethane emulsions with addition of isocyanate hardeners are resulted. The dependence of technological parameters of varnish application on the type and quantitative content of isocyanate hardener is described.
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Komar, V. V., T. A. Poсhodina, N. V. Kulinich, N. P. Krutko, and L. V. .Ovseenko. "Modification of water-suspension epoxy varnish and paint materials by nanostructured magnesium oxide." Proceedings of the National Academy of Sciences of Belarus, Chemical Series 56, no. 1 (2020): 105–13. http://dx.doi.org/10.29235/1561-8331-2020-56-1-105-113.

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The process of modifying aqueous powder suspension materials (APS) based on solid epoxy film-forming agents with highly dispersed powders of magnesium oxide was studied: production by ChemPur (n-MgO – primary size of particles is 36 nm), and magnesium oxide synthesized by a template method from the concentrated bischofite solution (MgOlab – primary size of particles is 102.8 nm). It was shown that presence of active functional surface OHgroups in both samples of magnesium oxide leads to the formation of secondary structures: aggregates and agglomerates. The nature of the influence of the size of aggregates of MgO particles and the conditions of dispersion on the properties of protective coatings is established. The nature of the influence of particle size and dispersion conditions on the properties of protective coatings is established. Optimal properties of coatings based on APS, sedimentation and aggregative stability of suspensions are implemented only under the condition of effective mechanical dispersion in a bead mill, when the most intensive destruction of large aggregates of n-MgO up to 50–60 nm occurs. The distribution of nanoparticle agglomerates in APS at the micro level (700–800 nm) using the MgO-lab does not lead to a significant change in the properties of APS and coatings based on them.It is shown that the introduction of n-MgO into APS allows reduces the curing temperature of the coatings from 110 to 90–100 °С. It is caused by the increase in the density of cross-linking of the spatial structure of polymer. The strength of modified coatings upon impact and tension increases by 2 times in comparison with the base composition, which does not contain nanomodifier, during curing of coatings at100 °C. In comparison with the known water-borne epoxy paints and varnishes, APS compositions are one-pack, they are more technological in use, have a long lifetime (up to 12 months in comparison with the viability of known two-pack epoxies, 1-8 hours). Materials can be used in industry for the protection of metal products, both as primers and as independent coatings.
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Nurlybayev, Ruslan E., Erzhan I. Kuldeyev, Zaure N. Altayeva, Zhanar O. Zhumadilova, Axaya S. Yestemessova, and Yelzhan S. Orynbekov. "Study of Properties of Water-Dispersion Paint and Varnish Compositions with the Content of Modified Mineral Filler." Coatings 14, no. 9 (2024): 1154. http://dx.doi.org/10.3390/coatings14091154.

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This article presents the results of research work devoted to improving the characteristics of paint and varnish coatings based on aqueous dispersions of polyacrylates; it is proposed to modify them by introducing mineral raw materials as fillers and hydrated lime, with subsequent processing in a vortex layer apparatus. The introduction of activated diatomite does not cause the deterioration of covering power, adhesion or an increase in the porosity of the paint material. The modification of coatings contributes to an increase in their operational properties, which can be associated with a reduction in the free volume in the composite and the formation of polymer boundary layers with modified physical and chemical properties. The aim of this study is to obtain a water-dispersion paint and varnish composition containing modified diatomite on a polyacrylate basis and, subsequently, study its main physical and mechanical parameters. The work has been carried out by the following method: determination of porosity, adhesion, elasticity and covering power of the control composition; determination of porosity, adhesion, elasticity and covering power of the obtained composites using modified filler; investigation of the influence of radiation on the infrared spectrum of the paint coating surface using a FLIRB620 thermal imager. As a result of this research work, it was noticed that the modification of water dispersions with silica-activated diatomite helps to eliminate the main disadvantages of materials and coatings based on acrylate binders—low water resistance and low physical and mechanical characteristics. The introduction of modified diatomite into water-emulsion paint on an acrylate base does not lead to the deterioration of the main performance characteristics of paint coatings—porosity, adhesion, elasticity and covering.
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Costanzo, Gary V., and Roger L. Kaesler. "Changes in Permian marine ostracode faunas during regression, Florena Shale, northeastern Kansas." Journal of Paleontology 61, no. 6 (1987): 1204–15. http://dx.doi.org/10.1017/s0022336000029577.

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The Florena Shale (Permian, Wolfcampian) of the Midcontinent of North America was deposited in a restricted marine basin. Shifting environments due to marine regression caused a gradual change in the ostracode fauna. Cluster analysis and ordination by nonmetric multidimensional scaling of data on ostracode relative abundances revealed three ostracode assemblages, each characteristic of a different environment. The Cryptobairdia seminalis assemblage from the lowest Florena Shale is characteristic of deeper water, offshore, marine environments with only minor influx of terrigenous mud. The Amphissites centronotus assemblage found above the C. seminalis assemblage occupied a similar environment, but with greater influx of terrigenous mud and intervals of increased turbidity. The Knightina texana assemblage occurs stratigraphically highest and probably represents a quiet-water, very shallow, nearshore, marine environment. Although protected from strong wave and current activity, the water mass was occasionally turbid.Species diversity of ostracodes is high both at the base of the Florena Shale, which was deposited in the most offshore position, and again at the top of the lower part of the Florena Shale, which was deposited nearer to the shore. In contrast to diversities of assemblages of ostracodes from similar environments in other stratigraphic units, the K. texana assemblage has an anomalously high diversity. This is due in part to time averaging of adjacent ostracode assemblages and a strong taphonomic overprint.
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Hedenquist, Jeffrey W., and Antonio Arribas. "Exploration Implications of Multiple Formation Environments of Advanced Argillic Minerals." Economic Geology 117, no. 3 (2022): 609–43. http://dx.doi.org/10.5382/econgeo.4880.

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Abstract Advanced argillic minerals, as defined, include alunite and anhydrite, aluminosilicates (kaolinite, halloysite, dickite, pyrophyllite, andalusite, zunyite, and topaz), and diaspore. One or more of these minerals form in five distinctly different geologic environments of hydrolytic alteration, with pH 4–5 to <1, most at depths <500 m. (1) Where an intrusion-related hydrothermal system, typical of that associated with porphyry Cu ± Au deposits, evolves to white-mica stability, continued ascent and cooling of the white-mica–stable liquid results in pyrophyllite (± diaspore) becoming stable near the base of the lithocap. (2) A well-understood hypogene environment of formation is vapor condensation near volcanic vents, where magmatic SO2 and HCl condense into local groundwater to produce H2SO4 and HCl-rich solutions with a pH of 1–1.5. Close to isochemical dissolution of the host rock occurs because of the high solubility of Al and Fe hydroxides at pH <2, except for the SiO2 component, which remains as a siliceous residue because of the relatively low solubility of SiO2. This residual quartz, commonly with a vuggy texture, is largely barren of metals because of the low metal content in high-temperature but low-pressure volcanic vapor. Rock dissolution causes the pH of the acidic solution to increase, such that alunite and kaolinite (or dickite or pyrophyllite at higher temperatures) become stable, forming a halo to the residual quartz. This initially barren residual quartz, which forms a lithocap horizon where permeable lithologic units are intersected by the feeder structure, may become mineralized if a subsequent white-mica–stable liquid ascends to this level and precipitates copper and gold. (3) Boiling of a hydrothermal liquid generates vapor with CO2 and H2S. Where the vapor condenses above the water table, atmospheric O2 in the vadose (unsaturated) zone causes oxidation of H2S to sulfuric acid, forming a steam-heated acid-sulfate solution with pH of 2–3. In this environment, kaolinite and alunite form in horizons above the water table at <100°C. Silica derived within the vadose zone will precipitate as amorphous silica at the water table, as the condensate follows the hydraulic gradient, causing opal replacement above and at the aquifer. (4) By contrast, where condensation of this vapor occurs below the water table, the CO2 in solution forms carbonic acid (H2CO3), leading to a pH of 4–5. This marginal carapace of condensate, with temperatures up to 150°–170°C, commonly acts as a diluent of the ascending parental NaCl liquid. This steam-heated liquid forms intermediate argillic alteration of clays, kaolinite, and Fe-Mn carbonates; this kaolinite, which can be present at depths of several hundreds of meters, can potentially be mistaken as having been caused by a steam-heated acid-sulfate or supergene overprint. (5) The final setting is supergene, caused by posthydrothermal weathering and oxidation of mainly pyrite, locally creating pH <1 liquid because of high concentrations of H2SO4 within the vadose zone and forming kaolinite, alunite, and Fe oxyhydroxides. This genetic framework of formation environments of advanced (and intermediate) argillic alteration provides the basis to interpret alteration mineralogy, in combination with alteration textures and morphology plus zonation, including the overprint of one alteration style on another. This framework can be used to help focus exploration for and assessment of hydrothermal ore deposits, including epithermal, porphyry, and volcanic-hosted massive sulfide.
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Conference papers on the topic "Water base overprint varnish"

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Żołek-Tryznowska, Zuzanna, and Marta Więcek. "Measurements of surface free energy as a tool to asses the effect of varnishing and printing of the paper substrates." In 10th International Symposium on Graphic Engineering and Design. University of Novi Sad, Faculty of technical sciences, Department of graphic engineering and design,, 2020. http://dx.doi.org/10.24867/grid-2020-p18.

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Nowadays, printing products might be finished in various ways. Varnishing process is one of the most popular finishing method which gives various effect, such as mate, glossy etc. However, the varnish layer applied on the paper is very thin, therefore it can be invisible to the naked human eye. The aim of this work was to use contact angle measurement and surface free energy determination as a tool to assess the effect of printing and varnishing process of paper materials. We have used various tools in order to analyses the changes of surface: surface roughness, gloss, water contact angle absorption and surface free energy determination. Those tools were used in order to confirm whether the print has been covered with varnish or not. In this work six various paper substrates were used (glossy, coated and un-coated papers). The printing and varnishing was performed in laboratory conditions using flexographic water-based printing and waterbased varnish. Samples were prepared as follows: paper with ink coating, paper with varnish coating and paper with ink layer and varnish layer on the top. The surface roughness was determinated of all samples and compared. The surface roughness changes were observed for pure paper, overprinted and overvarnished. Next, the gloss of samples prior and after printing and varnishing was measured. The gloss of the samples increases when they are printed or varnished, what is related with properties of ink and varnish. Also, the thickness of ink and varnish layers was determinated. The thickness of the samples increases when the number of layers increases. Finally, the water contact angle was measured and surface free energy was calculated with Owens-Wendt method. Our results reveal the possibility of using various tools in order to confirm the performance of varnishing of the prints. The printing with various colors is always seen by the naked human eye. On the other hand, the varnish layer might be not visible. However, such a comparison is not possible if we do not have the pure paper substrates prior printing or varnish.
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Andrade, Luciano G. D., Ezequiel C. P. Pessoa, Alexandre Q. Bracarense, Weslley C. Dias, Leandro F. Ribeiro, and Stephen Liu. "The Effect of Base Metal and Core Rod Carbon Content on Underwater Wet Weld Porosity." In ASME 2010 29th International Conference on Ocean, Offshore and Arctic Engineering. ASMEDC, 2010. http://dx.doi.org/10.1115/omae2010-20877.

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Porosity is a common defect observed in underwater wet welding. Several research programs have been developed to understand how pores form in order to mitigate the problem. No superficial pores and a limited number of internal pores (based on size) are important requirements to classify underwater wet welds according to the American Welding Society – AWS D3.6M standard. The main objective of this work is to study the effect of base metal and core rod carbon content on weld metal porosity. A pressure chamber with 20 atmospheres capacity was used to simulate depth with fresh water. To perform the welds, a gravity feeding system able to open an electric arc and deposit the weld automatically was used. Beads-on-plate were made using Direct Current Electrode Negative (DCEN) configuration on two base metals with different carbon contents (C2 – 0.1 wt. pct. and C7 – 0.7 wt. pct.) at 50 meters water depth. Commercial E6013 grade electrodes were used to deposit the welds. These electrodes were produced with core rods with two different carbon content (E2 – 0.002 wt. pct. and E6 – 0.6 wt. pct.) and painted with varnish for waterproofing. Samples were removed from the beginning, middle and end of the BOP welds and prepared following metallographic techniques including macroetching and image analysis for weld porosity. A data acquisition system was used to record current, voltage and welding time at 1.0 kHz rate. The porosity measurements indicated an increase of about 85% and 70% when E6 electrodes were used instead of E2 electrode on C2 and C7 steel plates, respectively. Simultaneously, the increase in porosity was followed by an increase in short circuiting events, an increase in weld bead penetration and a decrease in welding voltage. These observations seem to confirm, a direct effect of carbon content of the core rod on weld metal porosity and that porosity is associated with the CO reaction that can occur during metal transfer in that molten droplets carry gas bubbles to the welding pool. On the other hand, the increase of carbon content in the base metal was seen to decrease the porosity in the weld metal. This result can be related with the decrease in penetration observed when changing C2 to C7 plates. The smaller participation of carbon from the base metal in the weld pool reactions should then reduce the CO formation and, consequently, the amount of pores in the weld.
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Khan, Sara Hasrat, Wardah Arina Nasir, Hany El Sahn, et al. "Innovative High Permeability Streak Characterization and Modeling Utilizing Static and Dynamic Data in a Complex Giant Mature Oil Field in the Middle East." In Abu Dhabi International Petroleum Exhibition & Conference. SPE, 2021. http://dx.doi.org/10.2118/207310-ms.

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Abstract This paper proposes an integrated approach to model High Permeability Streaks (HPS) using the case study of heterogeneous carbonate Reservoir B, utilizing static and dynamic data. Modelling the HPS is critical as they play an important role in fluid dynamics within the reservoir. The impact is observed from 60 years of development, where flood front movement is captured by rich density of Pulsed Neutron and recently drilled open hole logs. Injection water is overriding from tighter lower subzones (injected zones) to permeable upper subzones of the reservoir, thereby leaving the tighter lower subzones unswept. Gas cusping down to the oil zone occurs through the HPS resulting in non-uniform gas cap expansion, which leads to early gas breakthrough in producers near the gas cap. The problem with characterizing HPS is associated with their thickness- in Reservoir B it ranges from 0.5 to 2.5ft and occur in multiple subzones in the upper part of the reservoir. The standard triple combo suite of logs does not have the resolution to detect these thin HPS. In addition, the cored interval of the HPS is mainly disintegrated which is attributed majorly to well sorted grain-supported lithofacies. Therefore, sampling for porosity & permeability via Routine Core Analysis (RCA) and Capillary pressure as well as pore throat distribution using Mercury Injection Capillary Pressure (MICP) method is extremely difficult. This results in a gap in the input dataset for the static models, where the higher permeability samples are not captured in logs or cores and are therefore under-represented. Current approach to unify this gap is to use permeability multipliers, which does not honor geological trends. The HPS in Reservoir B has added complexities when compared to other regional HPS. Not only are they multiple and distributed across subzones, there is also preferential movement of water through the HPS within the same area. Of the 3 upper subzones that have HPS, in some areas, water injected in lower subzone will override the HPS in the middle and move right to the HPS in the top subzone, thereby ignoring the hierarchical flood front movement from bottom to the top. A robust workflow was developed in order to address and resolve the above mentioned uncertainties related to High Permeability Streaks. The proposed integrated workflow consisted of five stages: Developing a robust geological conceptual model Mapping spatial distribution & continuity Capturing the vertical presence in cored & uncored wells (depth & thickness) Permeability Quantification of HPS using Well Test Measurements Modelling High Permeability Streaks The paper highlights the utilization of a range of static (core, Routine Core Analysis (RCA), image logs, OH logs) and dynamic data (Pulse Neutron Logs (PNL's), later drilled Open Hole Logs, Production Logging Tools (PLTs) and well test data). Quantitative (HPS depth indicated by water saturation profile indicated by waterflood movement) and Qualitative (Flooding observed but HPS depth is uncertain) depth indicators/flags were generated from the data set and became the foundation of the modelling the HPS. The first step in the workflow is to establish a robust geological conceptual model. For Reservoir B, certain facies contribute to HPS, which are mainly leached Rudist Rudstones and Coated grain Algal Floatstones as well as well sorted Skeletal Grainstones. Based on core observations, they have confirmed vertical stratigraphic presence in each subzone (top, mid, base) which is attributed to storm events. These were consequently mapped using average thickness from core descriptions and revised using contributing facies trend maps and qualitative dynamic observations. These maps served as basis for probability trend distribution for static rock type models. The vertical presence of HPS was increased from 10% to 30% by re-introducing them in the missing core intervals using quantitative dynamic flags and thickness from isochores. Consequently, permeability were assigned in the missing section using the proposed permeability enhancement technique that honors the verified well test measurements. Based on the above improvements, the HPS intervals were mapped to the static rock type with best reservoir quality (SRT 1), which is also linked to certain geological attributes (i.e. lithofacies, diagenetic overprint & depositional environment). The enhanced permeability in the identified HPS intervals is also reflected as upgraded SRT (from lower SRT 2 to best SRT 1). The overall impact is observed by improvement of poro-perm cloud, with added control points for HPS SRT (1), which is vital for permeability modelling. The updated permeability model, captures high perm streaks in terms of vertical presence and magnitude. By introducing higher permeability in the upper subzones of the reservoir, the water overriding/gas cusping phenomena could then be mimicked in the dynamic model. The proposed methodology is an integrated workflow that maximizes the input from each disciplines (G&G, Petrophysics and Reservoir Engineering) to create a robust static model through incorporation of high permeability streaks. The use static and dynamic data, has helped to establish HPS existence/preference, which then could be used to upgrade the permeability/SRT. This will in turn lead to a better static model and a better history match in the dynamic model. It will also led to better remaining in place prediction and enable accurate prediction for future field development, especially where EOR is involved.
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