Performance Products DIGLYCOLAMINE® Agent Product Information Huntsman DIGLYCOLAMINE® Agent Table of Contents Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . Sales Specifications . . . . . . . . . . . . . . . . . . . . Analytical Procedures . . . . . . . . . . . . . . . . . . . Applications . . . . . . . . . . . . . . . . . . . . . . . . . . Gas Treating Applications . . . . . . . . . . . . . Acid Gas Loading . . . . . . . . . . . . . . . . Regeneration Heat Requirements . . . . . Chemical and Thermal Degradation . . . DIGLYCOLAMINE® Product Reclaiming . . . . . . . . . . . . . . . . .2 .3 .3 .4 .4 .4 .5 .5 . . .5 Construction Materials . . . . . . . . . . . . . . . .7 Other Applications . . . . . . . . . . . . . . . . . . . . . . . .7 Physical Properties . . . . . . . . . . . . . . . . . . . . . .10 Chemical Properties . . . . . . . . . . . . . . . . . . . . . .45 Handling and Storage . . . . . . . . . . . . . . . . . . . . .46 General . . . . . . . . . . . . . . . . . . . . . . . . . . . .46 Maintaining Specifications . . . . . . . . . . . . . .46 Transfer Lines . . . . . . . . . . . . . . . . . . . . . . .46 Pumps . . . . . . . . . . . . . . . . . . . . . . . . . . . . .47 Unloading in Cold Weather . . . . . . . . . . . . . .47 New Facilities and Cleaning . . . . . . . . . . . . .47 Toxicity and Safety . . . . . . . . . . . . . . . . . . . . . .49 Shipping Information . . . . . . . . . . . . . . . . . . . . .50 Bibliography . . . . . . . . . . . . . . . . . . . . . . . . . . .51 Huntsman Sales Offices . . . . . . . . . . . . . . . . . .52 1 Introduction Huntsman's Gas Treating business is a leading global supplier of gas treating chemicals, supplying a wide range of chemicals to the gas conditioning industry for the removal of hydrogen sulfide and carbon dioxide in refinery as well as in produced gas streams. Continuous research and development helps our customers find more effective ways to solve their gas treating requirements. In addition we provide the necessary marketing, sales, manufacturing and technical support to supply customers with the right products at the right time and at a competitive price. DIGLYCOLAMINE® AGENT (DGA®) Huntsman is one of the largest global producers of specialty amines, with an annual capacity exceeding 90 million pounds. The DIGLYCOLAMINE® Agent (DGA®) can be reacted with fatty acids to form amides and amine salts for foam-boosting surfactants, stabilizers, detergents, and LAS emulsifying and wetting agents in shampoos, metalworking, paper treating and textile operations. The DIGLYCOLAMINE® (DGA®) brand of 2-(2aminoethoxy) ethanol is a critical component in the removal of hydrogen sulfide and/or carbon dioxide from gas streams. In addition to supplying this market, Huntsman is a leader in supplying this proven technology in increasing quantities for paint strippers, photoresist strippers for electronic circuit boards, 2 specialty surfactants, corrosion inhibitors, cutting fluids, amides, and other applications where primary amines are useful. Physically, DIGLYCOLAMINE agent is a clear, viscous liquid at room temperature and a white crystalline solid below its freezing point of 9.5°F (-12.5°C). DIGLYCOLAMINE agent has a relatively high boiling point and low vapor pressure. It is hygroscopic and miscible with water, most alcohols, and most polyols. Aqueous solutions of DIGLYCOLAMINE agent are alkaline. Being bifunctional, DIGLYCOLAMINE agent reacts with acids to form esters or salts. Most areas of use for DIGLYCOLAMINE agent are dependent to some degree on these features. The use of DIGLYCOLAMINE agent solution for gas treatment purposes holds great promise, both in new plants and in the conversion of existing amine facilities to obtain either lower treatment costs or an inexpensive means of debottlenecking existing treating facilities. This technical brochure provides the latest available data on this proven DIGLYCOLAMINE agent to ensure optimum use, giving you the advantage in your present operations and new applications. The Chemical Abstracts Service Registry number for DIGLYCOLAMINE agent is 926-06-6. Sales Specifications / Analytical Procedures Sales Specifications The following sales specifications are subject to change without notice. Appropriate analytical procedures for these specifications may be found to the right. Method of Determination Appearance Clear liquid, substantially free from suspended matter ST-30.1 Boiling range ASTM, °C ST-32.1 IBP 216 min. 95% 226 max. Color, Pt-Co scale 35 max. ST-30.12 wt. % by titration 98 min. ST-5.5 Water, wt. % 0.5 max. ST-31.53 DIGLYCOLAMINE Agent, Analytical Procedures Abbreviated forms of the standard methods of test for use with DGA® agent specifications are presented here. Copies of the methods in detail are available from our Technical Services Section in The Woodlands, Texas, upon request. APPEARANCE (Method No. ST-30.1) is determined by visual inspection of DIGLYCOLAMINE agent in a 100-ml tall-form Nessler tube. BOILING RANGE (Method No. ST-32.1) is determined by a procedure similar to ASTM D 1078-63. COLOR (Method No. ST-30.12) is determined visually in a 40-ml tube with APHA color disc standards, or in a 100-ml tall-form Nessler tube with liquid platinum cobalt (APHA) standards. DIGLYCOLAMINE agent (Method No. ST-5.5) is determined by titrating a solution of DIGLYCOLAMINE agent with standard hydrochloric acid using methyl purple indicator. WATER (Method No. ST-31.53) is determined by the standard Karl Fischer method, the end point being detected electrometrically. 3 Applications Gas Treating Applications DIGLYCOLAMINE/DEA is widely used for the absorption of acid gases, such as hydrogen sulfide (H2S) and carbon dioxide (CO2), and has been accepted worldwide as a successful gas treating agent. The DGA agent brand of 2-(2-aminoethoxy)ethanol is also used for removal of carbonyl sulfide (COS) from aliphatic liquid hydrocarbon streams using a patented Huntsman Corporation process. Experience obtained during the commercial application of DIGLYCOLAMINE gas treating agent has proven that its use often results in significant savings over other sweetening processes when the acid gas content of the stream to be treated is greater than 1 mole %. Natural gas sweetening units now in operation are treating gas streams with CO2:H2S ratios varying from over 100:1 to 0.1:1. Several plants are processing gas streams having acid gas contents in excess of 30 mole % with DIGLYCOLAMINE agent. Hydrogen sulfide recovered in DIGLYCOLAMINE agent units is being converted to bright sulfur via the Claus process. Savings of 15 to 20% in capital investments for new plants have been made using DIGLYCOLAMINE agent as compared to monoethanolamine systems. A significant reduction in plant operating cost is also realized due to a 15 to 30% reduction in regeneration heat requirements for the treating solution. The lower circulation rate required when utilizing a 50 to 65 wt.% DIGLYCOLAMINE agent solution is the major factor in the reduction of capital and operating costs. DIGLYCOLAMINE agent is used for the removal of CO2 and/or H2S from both natural and refinery gas streams. It should also be considered for synthesis gas and flue gas streams although as with all amines used for gas treating, degradation due to the presence of oxygen must be taken into consideration. DIGLYCOLAMINE agent has been successfully utilized for removal of COS, CO2, and H2S from liquid hydrocarbon streams. When DIGLYCOLAMINE agent is used to treat liquid hydrocarbon streams, a water wash of the treated hydrocarbon liquid is recommended to minimize entrainment losses, particularly when amine concentrations above 25 wt.% are utilized. The use of DIGLYCOLAMINE agent in gas treating should not be confused with the much older glycolamine process, which uses a mixed ethanolamine-glycol solvent for simultaneous sweetening and dehydration. Although DIGLYCOLAMINE agent is hygroscopic at very high concentrations, it is not currently recommended for simultaneous sweetening and dehydration. The proper choice of DIGLYCOLAMINE agent concentration and acid gas loading is affected by gas stream composition, treating conditions, and acid gas ratios in much the same manner as other amine sweetening processes involving absorption with chemical reaction. While recommended design concentrations are 4 Applications between 50 - 60 wt. %, current commercial experience confirms the applicability of up to 75 wt. % DIGLYCOLAMINE agent systems. ACID GAS LOADING — Recommended acid gas loadings will vary significantly in terms of SCF of acid gas/ gallon of DIGLYCOLAMINE agent, depending on CO2:H2S ratios, construction materials, and solution concentrations. Gases containing low CO2:H2S ratios are much less corrosive to amine treating systems and can be loaded to higher levels without experiencing undue corrosion, as compared to gas streams having high CO2:H2S ratios. Gross acid gas loadings of 0.35 to 0.425 mole/mole of DIGLYCOLAMINE agent solution are the typical current commercial practice. Recent experience, however, indicates that higher loadings may be possible when treating gases with low CO2:H2S ratios. Residual acid gas loading of lean DIGLYCOLAMINE agent solutions will normally be in the range of 0.05 — 0.06 mole of acid gas per mole of DIGLYCOLAMINE agent solution for high CO2:H2S ratios. Lower residual acid gas loadings for lean DIGLYCOLAMINE agent solution are usually obtained with low CO2:H2S ratios. SECONDARY CHEMICAL REACTIONS — Often referred to as a degradation product, there is a secondary reaction product in DIGLYCOLAMINE agent gas treating solution known as N,N'bis(hydroxyethoxyethyl)urea (BHEEU). The BHEEU product is formed by the reaction of 2 moles of DIGLYCOLAMINE agent with 1 mole of either CO2 or COS. It is also possible to form an additional product by the reaction of 1 mole of either carbon disulfide (CS2) or COS with 2 moles of DIGLYCOLAMINE agent to form N,N'bis(hydroxyethoxyethyl)thiourea. Experience indicates the dominant reaction with COS will be to form BHEEU. Unlike many other amines, these secondary reactions between DIGLYCOLAMINE agent and CO2, COS, or CS2 are not true degradation products for they are reversible at temperatures typically used in reclaiming operations (350 to 355°F). These reactions are shown below: REGENERATION HEAT REQUIREMENTS — Regeneration heat requirements for DIGLYCOLAMINE agent solutions will be affected by the CO2:H2S ratio of the acid gas contained in the inlet gas stream in much the same manner as other amine solutions. For gas streams containing a high CO2:H2S ratio, 1.0 — 1.2 moles of water vapor per mole of total acid gas in the regenerator overhead is typically used to establish regenerator heat requirements. Gas streams containing low CO2:H2S ratios generally require more heat for solution regeneration. 5 Applications DIGLYCOLAMINE PRODUCT RECLAIMING — The reclaiming of DIGLYCOLAMINE agent is usually necessary to maintain a circulating solution free of contaminants and with low concentrations of the bis(hydroxyethoxyethyl)urea (BHEEU). Heat-stable salts can also be removed from the treating solution in the reclaiming step. Addition of a low-chloride content alkali to the reclaimer can be used to free any DIGLYCOLAMINE product tied up as a heat stable salt. The lengths of reclaiming cycles vary and are usually determined for each individual plant. Commercial experience indicates reclaiming cycles vary from a few weeks to as long as three months or more. Periodically, operators should visually check to make certain reclaiming operations are continuing at design conditions. A flow indicator should be installed in the DIGLYCOLAMINE agent feed and the supplemental water feed to the reclaimer. Also, instrumentation 6 should be provided to enable plant operators to determine the quantity of heat being supplied to the DIGLYCOLAMINE agent solution reclaimer. Improper reclaimer operation can result in increases in contaminants as well as higher degradation product concentrations. To determine DIGLYCOLAMINE agent reclaiming cycle times, samples of lean treating solution and the reclaimer liquid should be analyzed periodically for increases in contaminant levels. Increases in contaminant level will vary at each individual plant; therefore, a history of reclaiming operations must be developed. Our Technical Services team can aid customers in determining optimum reclaimer cycle times. It is recommended that the DIGLYCOLAMINE agent reclaimer be designed utilizing the same basic design techniques as those employed for monoethanolamine reclaimers, with several additional considerations: Applications • The reclaimer should typically be sized to handle a minimum of 0.5% of the circulating solution. Certain types of applications might require higher reclaiming rates. • To optimize degradation product reconversion, reclaiming temperatures should be maintained below 360°F and typically around 350 to 355°F. In order to minimize thermal degradation, supplemental water feed to the reclaimer is usually required to prevent the reclaiming temperature from exceeding the 360°F level. A portion of the regenerator reflux, steam condensate, or good quality make-up water can be used for this purpose. • Control of the DIGLYCOLAMINE agent feed to the reclaimer is usually accomplished by setting a constant heat input to the reclaimer. With a constant reclaimer heat duty, the reclaimer feed rate is controlled by the reclaimer kettle liquid level control. If steam is utilized as the heating medium, it is recommended that a sparging steam line be installed below the reclaimer tube bundle. • Availability of sparging steam is particularly advantageous at the end of the reclaiming cycle to prevent settling of the accumulated sludge and solids, which will reduce liquid circulation around the reclaimer tube bundle. Because relatively long reclaiming cycles can be realized, it is important that 8 to 12 inches of clearance be provided between the bottom of the reclaimer shell and the reclaimer tube bundle. This clearance will accommodate the buildup of solids and sludge. Reclaimer overhead vapors should be returned to the stripping still via a separate line and can provide a significant portion of the regeneration heat requirements. An extra nozzle for vapor reentry should be added four or five trays from the bottom of the regenerator when sour regenerator reflux is used as the supplemental water source for the reclaimer. CONSTRUCTION MATERIALS — The choice of construction materials for DIGLYCOLAMINE agent solution treating facilities is essentially the same as for monoethanolamine systems. Generally speaking, treating systems handling gas streams with high ratios of CO2:H2S are in much more corrosive service than streams with low ratios of CO2:H2S and similar loadings and temperatures. Where low CO2:H2S ratios are encountered, carbon steel is usually satisfactory. Recommendations for construction materials should be handled on an individual basis for the specific application. Additional assistance can be obtained through our Technical Services team. DIGLYCOLAMINE agent gas treating solution has distinct advantages over monoethanolamine and diethanolamine for plants operating in cold weather areas because heat tracing requirements are reduced. DIGLYCOLAMINE agent solutions containing 30 to 35 wt. % H2O are within the eutectic region of the freezing curve. Freezing points as low as -40°F have been determined on actual plant samples containing 30 to 40 wt. % H2O and various quantities of acid gas. Viscosities will, of course, be quite high at low temperatures. Normal operating solutions of 60% DIGLYCOLAMINE agent are pumpable at -10°F in many facilities. 7 Applications Other Applications DIGLYCOLAMINE agent is suggested for use in many applications where other alkanolamines, morpholine, or other amines have been utilized. It reacts with fatty acids to form amides and amine salts useful as surfaceactive agents, such as foam boosters and stabilizers, detergents, and emulsifying and wetting agents. The reference numbers used in the following paragraphs refer to the bibliography. Our laboratory data demonstrate that, in certain concentration ranges, DIGLYCOLAMINE agent imparts greater viscosities than triethanolamine in amine-neutralized linear alkylbenzene sulfonic acid formulations. This effect is quite advantageous in shampoos and other specialty detergent and emulsifier applications. Aqueous solutions of sulfonic acid neutralized with DIGLYCOLAMINE agent had the following viscosities at the indicated concentrations at 25°C: Active Ingredients, % 5 10 15 20 25 Triethanolamine salt, viscosity, SUS 5.5 9.9 64 728 4,725 DIGLYCOLAMINE agent salt, viscosity SUS 5.8 29.3 619 4,436 6,910 DIGLYCOLAMINE agent is used as an emulsifying agent to prepare metal-working lubricants that prevent carbon deposits and discoloration of the metal.51 Photoresist strippers are made using DIGLYCOLAMINE agent in conjunction with N-methylpyrolidone. DIGLYCOLAMINE agent solution use in shampoo formulations also results in reduced eye irritation. Polyurethane rubber with lower solution viscosity and higher film elongation and tensile strength is produced using DIGLYCOLAMINE agent instead of preparations using Sulfonyldiamine.52 Stanford Research Institute, under the direction of the Fats and Proteins Research Foundation, has developed a process using DIGLYCOLAMINE agent to make a tallow sulfate as a lime soap dispersant. Other applications for DIGLYCOLAMINE agent include its use as a component of paint strippers, hydraulic fluids, extractive solvents, paper treating and textile treating solutions, and dyes, as detailed below: 8 Applications DIGLYCOLAMINE agent is used in accelerator additives for alkaline paint stripping solutions. These products usually require much shorter contact times than more conventional alkaline paint stripping compositions.38, 45, 46, 48 Fire-resistant polyamide ester hydraulic fluids are produced by reacting DIGLYCOLAMINE agent with a dibasic acid or one of its derivatives, such as phthalic anhydride.50 Anhydrous mixtures of DIGLYCOLAMINE agent and other selective solvents are used to separate aromatic compounds from hydrocarbon liquids. Extraction or extractive distillation is employed. DIGLYCOLAMINE agent’s high boiling point makes it especially suitable for this application.36, 39, 42 DIGLYCOLAMINE agent is also used in the TherMEcel® process for protecting and stabilizing transformer insulation papers against thermal deterioration and decomposition products of transformer oil and other liquid dielectrics. The TherMEcel process was developed by the Thomas A. Edison Division of McGraw-Edison. In this process, newly formed paper is thoroughly impregnated with an aqueous solution of DIGLYCOLAMINE agent while still on the papermaking machine.37, 49 Textile-treating solutions containing DIGLYCOLAMINE agent help cellulosic fabrics retain their original finish.43 Liquid developers for diazo copying papers use DIGLYCOLAMINE agent to replace the NH3 developers that contribute to air and water pollution problems.44, 47, 53 DIGLYCOLAMINE agent is also employed as a stabilizer in diazo dye compounds for paper and cellulose fibers.40 For further information on the uses of DIGLYCOLAMINE agent, consult the bibliography. 9 Physical Properties The following physical properties are for DIGLYCOLAMINE agent, a product of Huntsman Corporation: Molecular Weight 105.14 Boiling point, 760 mm Hg, °C 221 Critical constants* Critical temperature, °C 401.4 Critical pressure, atm 42.98 Critical density, g/cc 0.322 Density, g/ml, 60°F 1.0585 77°F 1.0508 Flash point, Pensky-Martens closed cup, °F 255 Freezing point, °C -12.2 Heat of vaporization, 760 mm Hg, Btu/lb 219.14 lonization constant, 25°C, kb 3.6 x 10-5 Refractive index, nD, 20°C 1.4598 Specific gravity, 20/20°C 1.0560 Specific heat of liquid, Btu/lb/ °F, 60°F 0.571 180°F 0.623 Thermal conductivity, 68°F, Btu/hr, sq ft,°F/ft 0.121 Vapor pressure, 68°F, mm Hg <0.01 Viscosity, 60°F, cp 40 Weight, 60°F, Ib/gal 8.82 * Calculated Heat of Reaction of Hydrogen Sulfide and Carbon Dioxide with DIGLYCOLAMINE Agent Heats of reaction were determined on 95 wt. % DIGLYCOLAMINE agent in aqueous solution loaded to 0.2 moles of acid gas per mole of DIGLYCOLAMINE agent. H = -850 Btu per pound of CO2 H = - 674 Btu per pound of H2S 10 Heats of Solution 20.1 wt. % water in DGA agent 72.7 Btu per pound of water 20.2 wt. % DGA agent in water 25.4 Btu per pound of DGA agent Additional physical properties pertinent to handling and using DIGLYCOLAMINE agent are presented in the pages that follow. Properties were determined in the laboratory using DIGLYCOLAMINE agent manufactured by Huntsman Corporation. An attempt has been made to correlate values that appear in the literature. Dotted lines in the figures indicate extrapolation. Physical Properties Property Figure Vapor Pressure of Aqueous DGA Agent Solutions 1 Vapor-Liquid Equilibrium for Aqueous DGA Agent Solutions at Various Pressures 2 Vapor-Liquid Equilibrium for Aqueous DGA Agent Solutions at Various Pressures 3 Water Vapor Dew Points Over Aqueous DGA Agent Solutions Versus Temperature 4 Viscosity of DGA Agent Versus Temperature 5 Viscosity of Aqueous DGA Agent Solutions Versus Temperature 6 Effect of Acid Gas Loading on Kinematic Viscosity of an Aqueous 25 Wt. % DGA Agent Solution Versus Temperature 7 Effect of Acid Gas Loading on Kinematic Viscosity of an Aqueous 50 Wt. % DGA Agent Solution Versus Temperature 8 Effect of Acid Gas Loading on Kinematic Viscosity of an Aqueous 65 Wt. % DGA Agent Solution Versus Temperature 9 Effect of Acid Gas Loading on Kinematic Viscosity of an Aqueous 80 Wt. % DGA Agent Solution Versus Temperature 10 Effect of Temperature on Kinematic Viscosity of Aqueous DGA Agent Solutions Loaded to 0.1 Moles CO2/Mole DGA Agent 11 Effect of Temperature on Kinematic Viscosity of Aqueous DGA Agent Solutions Loaded to 0.2 Moles CO2/Mole DGA Agent 12 Effect of Temperature on Kinematic Viscosity of Aqueous DGA Agent Solutions Loaded to 0.4 Moles CO2/Mole DGA Agent 13 Effect of Temperature on Kinematic Viscosity of Aqueous DGA Agent Solutions Loaded to 0.2 Moles CO2 and 0.2 Moles H2S/Mole DGA Agent 14 Effect of Temperature on Kinematic Viscosity of Aqueous DGA Agent Solutions Loaded to 0.1 Moles CO2 and 0.3 Moles H2S/Mole DGA Agent 15 Density of DGA Agent Versus Temperature 16 Density of Aqueous DGA Agent Solution Versus Temperature 17 Effect of Acid Gas Loading on Density of an Aqueous 25 Wt. % DGA Agent Solution Versus Temperature 18 Effect of Acid Gas Loading on Density of an Aqueous 50 Wt. % DGA Agent Solution Versus Temperature 19 Effect of Acid Gas Loading on Density of an Aqueous 65 Wt. % DGA Agent Solution Versus Temperature 20 Effect of Acid Gas Loading on Density of an Aqueous 75 Wt. % DGA Agent Solution Versus Temperature 21 Effect of Acid Gas Loading on Density of an Aqueous 80 Wt. % DGA Agent Solution Versus Temperature 22 Effect of Temperature on Density of Aqueous DGA Agent Solutions Loaded to 0.2 Moles CO2/Mole DGA Agent 23 Effect of Temperature on Density of Aqueous DGA Agent Solutions Loaded to 0.4 Moles CO2/Mole DGA Agent 24 Effect of Temperature on Density of Aqueous DGA Agent Solutions Loaded to 0.1 Moles CO2 and 0.1 Moles H2S/Mole DGA Agent 25 Effect of Temperature on Density of Aqueous DGA Agent Solutions Loaded to 0.2 Moles CO2 and 0.2 Moles H2S/ Mole DGA Agent 26 Specific Heat of Aqueous DGA Agent Solutions Versus Temperature 27 Thermal Conductivity of Aqueous DGA Agent Solutions 28 Freezing Points of Aqueous DGA Agent Solutions 29 pH of Aqueous DGA Agent Solutions at 20°C 30 Surface Tension of Aqueous DGA Agent Solutions Versus Temperature 31 Hydrogen Solubility in Gas Treating Amine Solutions Versus Hydrogen Partial Pressure 32 Nitrogen Solubility in Aqueous 60 Wt. % DGA Agent Solution at 180°F 33 11 Physical Properties Figure 1 Vapor Pressure of Aqueous DIGLYCOLAMINE® Agent Solutions 3,000 Water 50 Wt. % DGA Agent 70 Wt. % DGA Agent 90 Wt. % DGA Agent 95 Wt. % DGA Agent 100 Wt. % DGA Agent 2,000 1,000 700 500 VAPOR PRESSURE, mm Hg 300 200 100 70 50 30 20 10 5 3 100 150 200 250 TEMPERATURE, °F 12 300 400 500 Physical Properties Figure 2 Vapor-Liquid Equilibrium for Aqueous DIGLYCOLAMINE® Agent Solutions at Various Pressures 440 420 400 380 360 340 760 mm Hg TEMPERATURE, °F 320 300 300 mm Hg 280 260 100 mm Hg 240 220 200 180 160 140 120 0 10 20 3 0 40 50 60 70 80 90 100 DIGLYCOLAMINE® AGENT, wt. % 13 Physical Properties Figure 3 Vapor-Liquid Equilibrium for Aqueous DIGLYCOLAMINE® Agent Solutions at Various Pressures 540 520 500 480 460 440 TEMPERATURE, °F 420 400 380 20 PSIA 360 25 PSIA 340 35 PSIA 320 300 280 260 240 220 0 10 20 3 0 40 50 60 70 DIGLYCOLAMINE® AGENT, wt. % 14 80 90 100 Physical Properties Figure 4 Water Vapor Dew Points Over Aqueous DIGLYCOLAMINE® Agent Solutions Versus Temperature 120 110 100 Water 50 Wt. % DGA Agent 70 Wt. % DGA Agent 80 Wt. % DGA Agent 90 Wt. % DGA Agent 95 Wt. % DGA Agent 97 Wt. % DGA Agent 98 Wt. % DGA Agent 99 Wt. % DGA Agent 90 WATER VAPOR DEW POINT, °F 80 70 60 50 40 30 20 10 0 –10 –20 75 80 85 90 95 100 105 110 115 120 125 TEMPERATURE, °F 15 Physical Properties Figure 5 Viscosity of DIGLYCOLAMINE® Agent Versus Temperature 100 90 80 70 60 50 40 30 VISCOSITY, cp 20 10 9 8 7 6 5 4 3 2 1 50 100 150 200 TEMPERATURE, °F 16 250 300 Physical Properties Figure 6 Viscosity of Aqueous DIGLYCOLAMINE® Agent Solutions Versus Temperature 100,000.0 Freezing Point Curve –40°F 10,000.0 –20°F 1,000.0 VISCOSITY, cp 0°F 20°F 100.0 40°F 60°F 80°F 100°F 120°F 10.0 140°F 160°F 180°F 200°F 1.0 0.1 0 10 20 30 40 50 60 70 80 90 100 DIGLYCOLAMINE® AGENT, wt. % 17 Physical Properties Figure 7 Effect of Acid Gas Loading on Kinematic Viscosity of an Aqueous 25 Wt. % DIGLYCOLAMINE® Agent Solution Versus Temperature 4.00 (24 Wt. % DGA Agent); 0.38 Moles CO 2/MOLE DGA Agent (24 Wt. % DGA Agent); 0.19 Moles CO 2/MOLE DGA Agent (25 Wt. % DGA Agent); no CO 2 3.00 2.00 KINEMATIC VISCOSITY, cSt 1.50 1.25 1.00 0.90 0.80 0.70 0.60 0.50 50 75 100 125 150 TEMPERATURE, °F 18 175 200 225 250 Physical Properties Figure 8 Effect of Acid Gas Loading on Kinematic Viscosity of an Aqueous 50 Wt. % DIGLYCOLAMINE® Agent Solution Versus Temperature 30.00 (44.8 Wt. % DGA Agent); 0.41 Moles CO2/Mole DGA Agent (47.2 Wt. % DGA Agent); 0.19 Moles CO2/Mole DGA Agent (49.6 Wt. % DGA Agent); no CO 2 (48.6 Wt. % DGA Agent); 0.10 Moles CO2/Mole DGA Agent (46.0 Wt. % DGA Agent); 0.21 Moles CO2/Mole DGA Agent and 0.23 Moles H2S/Mole DGA Agent (46.6 Wt. % DGA Agent); 0.11 Moles CO2/Mole DGA Agent and 0.29 Moles H2S/Mole DGA Agent 20.00 15.00 10.00 9.00 8.00 7.00 6.00 5.00 KINEMATIC VISCOSITY, cSt 4.00 3.00 2.00 1.75 1.50 1.25 1.00 0.90 0.80 50 75 100 125 150 175 200 225 250 TEMPERATURE, °F 19 Physical Properties Figure 9 Effect of Acid Gas Loading on Kinematic Viscosity of an Aqueous 65 Wt. % DIGLYCOLAMINE® Agent Solution Versus Temperature 100.00 (57.0 Wt. % DGA Agent); 0.42 Moles CO2/Mole DGA Agent (58.7 Wt. % DGA Agent); 0.20 Moles CO2/Mole DGA Agent and 0.21 Moles H2S/Mole DGA Agent (60.9 Wt. % DGA Agent); 0.20 Moles CO2/Mole DGA Agent (59.4 Wt. % DGA Agent); 0.10 Moles CO2/Mole DGA Agent and 0.30 Moles H2S/Mole DGA Agent (62.6 Wt. % DGA Agent); 0.10 Moles CO2/Mole DGA Agent (64.4 Wt. % DGA Agent); no CO 2 75.00 50.00 40.00 30.00 20.00 KINEMATIC VISCOSITY, cSt 15.00 10.00 9.00 8.00 7.00 6.00 5.00 4.00 3.00 2.00 1.75 1.50 1.25 50 75 100 125 150 TEMPERATURE, °F 20 175 200 225 250 Physical Properties Figure 10 Effect of Acid Gas Loading on Kinematic Viscosity of an Aqueous 80 Wt. % DIGLYCOLAMINE® Agent Solution Versus Temperature 1,000.0 (69.0 Wt. % DGA Agent); 0.42 Moles CO2/Mole DGA Agent (71.2 Wt. % DGA Agent); 0.20 Moles CO2/Mole DGA Agent and 0.21 Moles H2S/Mole DGA Agent (72.0 Wt. % DGA Agent); 0.10 Moles CO2/Mole DGA Agent and 0.30 Moles H2S/Mole DGA Agent (73.6 Wt. % DGA Agent); 0.20 Moles CO2/Mole DGA Agent (76.9 Wt. % DGA Agent); 0.10 Moles CO2/Mole DGA Agent (79.5 Wt. % DGA Agent); no CO 2 500.0 100.0 75.0 50.0 KINEMATIC VISCOSITY, cSt 40.0 30.0 20.0 10.0 8.0 6.0 5.0 4.0 3.0 2.0 50 75 100 125 150 175 200 225 250 TEMPERATURE, °F 21 Physical Properties Figure 11 Effect of Temperature on Kinematic Viscosity of Aqueous DIGLYCOLAMINE® Agent Solutions Loaded to 0.1 Moles CO2 /Mole DGA Agent 100 90 80 70 60°F 80°F 100°F 120°F 140°F 160°F 180°F 60 50 40 30 KINEMATIC VISCOSITY, cSt 20 10 9 8 7 6 5 4 3 2 Solutions of 50, 65, and 80 wt. % DGA agent were loaded to 0.1 moles CO2/mole DGA agent to obtain this family of curves. 1 0 10 20 30 40 50 60 DIGLYCOLAMINE® AGENT, wt. % 22 70 80 90 100 Physical Properties Figure 12 Effect of Temperature on Kinematic Viscosity of Aqueous DIGLYCOLAMINE® Agent Solutions Loaded to 0.2 Moles CO2 /Mole DGA Agent 100 90 80 70 60°F 80°F 100°F 120°F 140°F 160°F 180°F 60 50 40 30 KINEMATIC VISCOSITY, cSt 20 10 9 8 7 6 5 4 3 Solutions of 25, 50, 65, and 80 wt. % DGA agent were loaded to 0.2 moles CO2/mole DGA agent to obtain this family of curves. 2 1 0 10 20 30 40 50 60 70 80 90 100 DIGLYCOLAMINE® AGENT, wt. % 23 Physical Properties Figure 13 Effect of Temperature on Kinematic Viscosity of Aqueous DIGLYCOLAMINE® Agent Solutions Loaded to 0.4 Moles CO2 /Mole DGA Agent 1,000 800 60°F 80°F 100°F 120°F 140°F 160°F 180°F 600 500 400 300 200 100 KINEMATIC VISCOSITY, cSt 80 60 50 40 30 20 10 8 6 5 4 Solutions of 25, 50, 65, and 80 wt. % DGA agent were loaded to 0.4 moles CO2/mole DGA agent to obtain this family of curves. 3 2 1 0 10 20 30 40 50 60 70 DIGLYCOLAMINE® AGENT, wt. % 24 80 90 100 Physical Properties Figure 14 Effect of Temperature on Kinematic Viscosity of Aqueous DIGLYCOLAMINE® Agent Solutions Loaded to 0.2 Moles CO2 and 0.2 Moles H2S/Mole DGA Agent 100 90 80 70 60°F 80°F 100°F 120°F 140°F 160°F 180°F 60 50 40 30 KINEMATIC VISCOSITY, cSt 20 10 9 8 7 6 5 4 3 2 Solutions of 50, 65, and 80 wt. % DGA agent were loaded to 0.2 moles CO2 and 0.2 moles H2S/mole DGA agent to obtain this family of curves. 1 0 10 20 30 40 50 60 70 80 90 100 DIGLYCOLAMINE® AGENT, wt. % 25 Physical Properties Figure 15 Effect of Temperature on Kinematic Viscosity of Aqueous DIGLYCOLAMINE® Agent Solutions Loaded to 0.1 Moles CO2 and 0.3 Moles H2S/Mole DGA Agent 100 90 80 70 60°F 80°F 100°F 120°F 140°F 160°F 180°F 60 50 40 30 KINEMATIC VISCOSITY, cSt 20 10 9 8 7 6 5 4 3 2 Solutions of 50, 65, and 80 wt. % DGA agent were loaded to 0.1 moles CO2 and 0.3 moles H2S/mole DGA agent to obtain this family of curves. 1 0 10 20 30 40 50 60 DIGLYCOLAMINE® AGENT, wt. % 26 70 80 90 100 Physical Properties Figure 16 Density of DIGLYCOLAMINE® Agent Versus Temperature 1.13 1.12 1.11 1.10 1.09 1.08 1.07 1.06 1.05 DENSITY, g/cc 1.04 1.03 1.02 1.01 1.00 0.99 0.98 0.97 0.96 0.95 0.94 0.93 0.92 0.91 0.90 0 20 40 60 80 100 120 140 160 180 200 220 240 260 280 300 TEMPERATURE, °F 27 Physical Properties Figure 17 Density of Aqueous DIGLYCOLAMINE® Agent Solution Versus Temperature 1.13 Freezing Point Curve 1.12 –40°F 1.11 –20°F 1.10 0°F 1.09 20°F 1.08 40°F 60°F DENSITY, g/cc 1.07 80°F 1.06 100°F 1.05 120°F 1.04 140°F 1.03 160°F 1.02 180°F 1.01 1.00 0.99 0.98 0.97 0 10 20 30 40 50 60 70 DIGLYCOLAMINE® AGENT, wt. % 28 80 90 100 Physical Properties Figure 18 Effect of Acid Gas Loading on Density of an Aqueous 25 Wt. % DIGLYCOLAMINE® Agent Solution Versus Temperature 1.160 (24 wt. % DGA Agent); 0.38 Moles CO2/Mole DGA Agent (24.1 wt. % DGA Agent); 0.21 Moles CO2/Mole DGA Agent and 0.20 Moles H2S/Mole DGA Agent (24.6 wt. % DGA Agent); 0.19 Moles CO2/Mole DGA Agent (24.4 wt. % DGA Agent); 0.09 Moles CO2 and 0.11 Moles H2S/Mole DGA Agent (25 wt. % DGA Agent); no CO2 1.140 1.120 DENSITY, g/cc 1.100 1.080 1.060 1.040 1.020 1.000 0.980 80 100 120 140 160 180 TEMPERATURE, °F 29 Physical Properties Figure 19 Effect of Acid Gas Loading on Density of an Aqueous 50 Wt. % DIGLYCOLAMINE® Agent Solution Versus Temperature 1.160 (44.8 wt. % DGA Agent); 0.41 Moles CO2/Mole DGA Agent (46.6 wt. % DGA Agent); 0.18 Moles CO2 and 0.21 Moles H2S/Mole DGA Agent (47.2 wt. % DGA Agent); 0.19 Moles CO2/Mole DGA Agent (48.1 wt. % DGA Agent); 0.11 Moles CO2 and 0.11 Moles H2S/Mole DGA Agent (49.6 wt. % DGA Agent); no CO2 1.140 1.120 DENSITY, g/cc 1.100 1.080 1.060 1.040 1.020 1.000 0.980 80 100 120 140 TEMPERATURE, °F 30 160 180 Physical Properties Figure 20 Effect of Acid Gas Loading on Density of an Aqueous 65 Wt. % DIGLYCOLAMINE® Agent Solution Versus Temperature 1.160 1.140 1.120 DENSITY, g/cc 1.100 1.080 1.060 1.040 1.020 (57.0 wt. % DGA Agent); 0.42 Moles CO2/Mole DGA Agent (60.9 wt. % DGA Agent); 0.20 Moles CO2/Mole DGA Agent (64.4 wt. % DGA Agent); no CO2 1.000 0.980 80 100 120 140 160 180 TEMPERATURE, °F 31 Physical Properties Figure 21 Effect of Acid Gas Loading on Density of an Aqueous 75 Wt. % DIGLYCOLAMINE® Agent Solution Versus Temperature 1.160 1.140 1.120 DENSITY, g/cc 1.100 1.080 1.060 1.040 (66.7 wt. % DGA Agent); 0.40 Moles CO2/Mole DGA Agent (67.8 wt. % DGA Agent); 0.20 Moles CO2 and 0.18 Moles H2S/Mole DGA Agent (71.0 wt. % DGA Agent); 0.18 Moles CO2/Mole DGA Agent (71.1 wt. % DGA Agent); 0.09 Moles CO2 and 0.10 Moles H2S/Mole DGA Agent (75 wt. % DGA Agent); no CO2 1.020 1.000 0.980 80 100 120 140 TEMPERATURE, °F 32 160 180 Physical Properties Figure 22 Effect of Acid Gas Loading on Density of an Aqueous 80 Wt. % DIGLYCOLAMINE® Agent Solution Versus Temperature 1.180 1.160 1.140 DENSITY, g/cc 1.120 1.100 1.080 1.060 1.040 (67.9 wt. % DGA Agent); 0.42 Moles CO2/Mole DGA Agent (73.5 wt. % DGA Agent); 0.20 Moles CO2/Mole DGA Agent (79.5 wt. % DGA Agent); no CO2 1.020 1.000 80 100 120 140 160 180 TEMPERATURE, °F 33 Physical Properties Figure 23 Effect of Temperature on Density of Aqueous DIGLYCOLAMINE® Agent Solutions Loaded to 0.2 Moles CO2 /Mole DGA Agent 1.13 60°F Solutions of 25, 50, 65, and 80 wt. % DGA agent were loaded to 0.2 moles CO2/mole DGA agent to obtain this family of curves. 1.12 1.11 80°F 100°F 120°F 1.10 140°F 1.09 160°F 1.08 180°F DENSITY, g/cc 1.07 1.06 1.05 1.04 1.03 1.02 1.01 1.00 0.99 0.98 0.97 0 10 20 30 40 50 60 70 DIGLYCOLAMINE® AGENT, wt. % 34 80 90 100 Physical Properties Figure 24 Effect of Temperature on Density of Aqueous DIGLYCOLAMINE® Agent Solutions Loaded to 0.4 Moles CO2 /Mole DGA Agent 1.20 1.19 Solutions of 25, 50, 65, and 80 wt. % DGA agent were loaded to 0.4 moles CO2/mole DGA agent to obtain this family of curves. 1.18 1.17 60°F 80°F 100°F 120°F 140°F 1.16 1.15 160°F 1.14 180°F 1.13 1.12 1.11 DENSITY, g/cc 1.10 1.09 1.08 1.07 1.06 1.05 1.04 1.03 1.02 1.01 1.00 0.99 0.98 0.97 0.96 0 10 20 30 40 50 60 70 80 90 100 DIGLYCOLAMINE® AGENT, wt. % 35 Physical Properties Figure 25 Effect of Temperature on Density of Aqueous DIGLYCOLAMINE® Agent Solutions Loaded to 0.1 Moles CO2 and 0.1 Moles H2S/Mole DGA Agent 1.13 Solutions of 25, 50, and 75 wt. % DGA agent were loaded to 0.1 moles CO2 and 0.1 moles H2S/mole DGA agent to obtain this family of curves. 1.12 1.11 60°F 1.10 80°F 1.09 100°F 120°F 1.08 140°F 1.07 DENSITY, g/cc 160°F 1.06 180°F 1.05 1.04 1.03 1.02 1.01 1.00 0.99 0.98 0.97 0 10 20 30 40 50 60 70 DIGLYCOLAMINE® AGENT, wt. % 36 80 90 100 Physical Properties Figure 26 Effect of Temperature on Density of Aqueous DIGLYCOLAMINE® Agent Solutions Loaded to 0.2 Moles CO2 and 0.2 Moles H2S/Mole DGA Agent 1.15 Solutions of 25, 50, and 75 wt. % DGA agent were loaded to 0.2 moles CO2 and 0.2 moles H2S/mole DGA agent to obtain this family of curves. 1.14 1.13 60°F 80°F 100°F 1.12 120°F 1.11 140°F 1.10 160°F 1.09 180°F DENSITY, g/cc 1.08 1.07 1.06 1.05 1.04 1.03 1.02 1.01 1.00 0.99 0.98 0.97 0 10 20 30 40 50 60 70 80 90 100 DIGLYCOLAMINE® AGENT, wt. % 37 Physical Properties Figure 27 Specific Heat of Aqueous DIGLYCOLAMINE® Agent Solutions Versus Temperature 340 320 300 Water 50 Wt. % DGA Agent 60 Wt. % DGA Agent 70 Wt. % DGA Agent 80 Wt. % DGA Agent 90 Wt. % DGA Agent DGA Agent 280 260 TEMPERATURE, °F 240 220 200 180 160 140 120 100 80 60 1.05 1.00 0.95 0.90 0.85 0.80 0.75 SPECIFIC HEAT, Btu/lb/°F 38 0.70 0.65 0.60 0.55 Physical Properties Figure 28 Thermal Conductivity of Aqueous DIGLYCOLAMINE® Agent Solutions 0.45 0.40 Water 20 Wt. % DGA Agent 40 Wt. % DGA Agent 60 Wt. % DGA Agent 80 Wt. % DGA Agent DGA Agent Boiling Point Curve THERMAL CONDUCTIVITY, Btu/hr, sq ft, °F/ft 0.35 0.30 0.25 0.20 0.15 0.10 50 100 150 200 250 TEMPERATURE, °F 39 Physical Properties Figure 29 Freezing Points of Aqueous DIGLYCOLAMINE® Agent Solutions 80 70 60 50 40 FREEZING POINT, °F 30 20 10 0 –10 –20 –30 –40 –50 –60 0 10 20 3 0 40 50 60 DIGLYCOLAMINE® AGENT, wt. % 40 70 80 90 100 Physical Properties Figure 30 pH of Aqueous DIGLYCOLAMINE® Agent Solutions at 20° C 100.0 70.0 50.0 40.0 30.0 20.0 DIGLYCOLAMINE® AGENT, wt. % 10.0 7.0 5.0 4.0 3.0 2.0 1.0 0.7 0.5 0.4 0.3 0.2 0.1 10 11 12 13 14 pH 41 Physical Properties Figure 31 Surface Tension of Aqueous DIGLYCOLAMINE® Agent Solutions Versus Temperature 80 75 70 65 SURFACE TENSION, dynes/cm 60 55 50 45 40 35 30 25 20 Water 50 Wt. % DGA Agent 75 Wt. % DGA Agent DGA Agent 15 10 50 60 70 80 90 100 110 TEMPERATURE, °F 42 120 130 140 150 Physical Properties Figure 32 Hydrogen Solubility in Gas Treating Amine Solutions Versus Hydrogen Partial Pressure 0.90 Hydrogen solubility in 20 wt. % MEA-water solution at 144°F Hydrogen solubility in 60 wt. % DGA agent-water solution at 180°F 0.80 HYDROGEN SOLUBILITY, cu ft/gal DGA agent 0.70 0.60 0.50 0.40 0.30 0.20 0.10 0.00 0 40 80 120 160 200 240 280 320 360 400 HYDROGEN PARTIAL PRESSURE, psia 43 Physical Properties Figure 33 Nitrogen Solubility in Aqueous 60 Wt. % DIGLYCOLAMINE® Agent Solution at 180°F 0.90 0.80 NITROGEN SOLUBILITY, cu ft/gal DGA agent 0.70 0.60 0.50 0.40 0.30 0.20 0.10 0.00 0 40 80 120 160 200 240 280 NITROGEN PARTIAL PRESSURE, psia 44 320 360 400 Chemical Properties DIGLYCOLAMINE agent undergoes reactions typical of alcohols and amines. It is isomeric with diethanolamine; however, it has certain structural differences that are advantageous in some applications. For example, DIGLYCOLAMINE agent is a primary amine, whereas diethanolamine is a secondary amine. The primary NH2 group makes DIGLYCOLAMINE agent more reactive than diethanolamine. In certain reactions, such as those involving CO2, DIGLYCOLAMINE agent will have an advantage over the primary amine, monoethanolamine, in avoiding cyclic structures. 45 Handling and Storage General Steam coils with sufficient surface area to heat the The handling and storage of DIGLYCOLAMINE agent tank contents using low-pressure steam should be presents no unusual problems. Our Technical built into the tank about six inches above the floor. The Service staff is available to assist those persons coils should be constructed in such a manner as to desiring additional information. See the Toxicity and allow the condensate to drain. Stainless steel coils are Safety section for related additional information. preferred, particularly when low color DIGLYCOLAMINE agent solution is important. If steam heat is to Maintaining Specifications be used continuously to prevent high viscosities or DIGLYCOLAMINE agent is hygroscopic and will freezing, a temperature regulator that throttles either absorb water vapor when exposed to a moist the steam or condensate should be installed. atmosphere. If water content is to be minimized, a dry inert gas pad under a few ounces of pressure In situations where the ambient temperature is low, should be used on the storage tanks. A gas pad tank insulation is desirable. Asphalt-cork or urethane should also be used if low color is important, since foam insulation sprayed onto the outer wall is satisfac- absorbed atmospheric oxygen and carbon dioxide tory. If a nitrogen pad is used, pressure relief and vacu- will cause DIGLYCOLAMINE agent to develop color. um relief valves of a suitable capacity should be Since DIGLYCOLAMINE agent is basic, it will react installed. The system may consist of a cylinder of nitro- with acidic gases, hence carbon dioxide and natural gen, a pressure reducing valve, a pressure relief valve, gas containing acidic sulfur compounds cannot be and a line to the top of the storage tank. Tankage used. Nitrogen is quite suitable. should be diked and electrically bonded and grounded. The solvent properties and alkaline nature of DIGLY- In cold climates, when DIGLYCOLAMINE agent is uti- COLAMINE agent should also be considered when lized for gas treating applications, it can be diluted installing handling and storage facilities. DIGLYCO- with water to approximately 80% concentration. An 80 LAMINE agent will react with copper to form com- wt. % DlGLYCOLAMINE agent:water solution has a plex salts. The use of copper and alloys containing freezing point below -40°F. copper should be avoided in equipment that will contact DIGLYCOLAMINE agent or its aqueous solu- Transfer Lines tions. Carbon steel storage tanks constructed Carbon steel transfer lines at least two inches in diam- according to a recognized code are generally satis- eter and joined by welds or flanges are suitable. factory. In cases where low color is important, stain- Screwed joints are subject to failure unless back-weld- less steel is preferred. ed because DIGLYCOLAMINE agent will leach conventional pipe dopes. U.S. Rubber 899 gasket material or DIGLYCOLAMINE agent is not compatible with phe- its equivalent is satisfactory for use with flanged con- nolic resin linings. nections in DIGLYCOLAMINE agent service. 46 Handling and Storage If the ambient temperature is below 20°F, the transfer Because DIGLYCOLAMINE agent has high viscosi- line for the pure product should be steam traced and ties at low temperatures, provision should be made insulated. Steam tracing can be accomplished by for preheating pumps exposed to the cold. To pre- affixing copper tubing of approximately 3/8-inch heat pumps, install steam tracing and apply low- diameter to the underside of the line, insulating the pressure steam to the tubing. tube to the line, and using low-pressure steam in the tubing. For flexible connections, stainless steel hose Unloading in Cold Weather is preferred to rubber, since rubber will generally Thawing a tank or tank car of DIGLYCOLAMINE deteriorate in DIGLYCOLAMINE agent service and agent is accomplished by applying steam at 50 increase the color of the product with time and tem- pounds pressure maximum to the coils of the tank perature. Systems that are insulated and steam- or tank car. Product temperature should be kept traced should be preheated in cool weather before below 150°F. being put into service. Normally, 15 to 30 minutes of applying steam to the tubing will adequately warm, Thawing may be accelerated by using a liquid circu- but not overheat, the system. Transfer piping and lating pump. In the case of unloading tank cars, or if pumps may be equipped with a nitrogen padding steam is being discontinued to tanks, the coils system so the DIGLYCOLAMINE agent can be pres- should be blown free of condensate with dry air to sured out of the lines when an extended idle period prevent freezing of the condensate and coil rupture. is contemplated. This practice will help reduce losses For further information on handling frozen product in and color increases that would result if the DIGLYCO- tanks, it is recommended that reference be made to LAMINE agent were allowed to remain in the lines. Association of American Railroads’ Pamphlet No. 34, and General American Transportation Corporation’s Pumps “Care of Heater Coils in Tank Cars.” Carbon steel rotary pumps can be used with DIGLYCOLAMINE agent, although a centrifugal pump is DIGLYCOLAMINE agent that has frozen in drums preferred. Rotary pumps should be equipped with may be thawed in a hot room at about 100° F. externally lubricated bearings. A Durametallic Type Thawing should be expected to require approximate- RO-TT mechanical seal is suitable. Where pump ly two to three days. packing is required, Garlock 234, Garlock 239, or equivalent is satisfactory. 47 Handling and Storage New Facilities and Cleaning tank should not be wire brushed or sandblasted Prior to putting storage vessels into service, it is because the oxides of iron are relatively inert to desirable to purge with nitrogen to remove oxygen DIGLYCOLAMINE agent. Once clean and dry, the from the tank atmosphere. Although frequent clean- tank should be sealed and purged with dry nitrogen ing of tanks and transfer lines is not recommended, to avoid undue condensation and rust formation. it may be necessary due to contamination or accu- Most of what has been described so far is con- mulation of foreign material in the system. For such cerned with commercial, essentially anhydrous, cleaning, a water wash is generally satisfactory. DIGLYCOLAMINE agent. Aqueous DIGLYCOLAMINE agent solutions have lower freezing points and lower Tank cleaning is normally accomplished by thorough- viscosities, so storage and handling may be simpli- ly sluicing the interior of the tank with a water jet, fied considerably by dilution in storage if the DIGLY- followed by cloth or chamois drying. Unless exces- COLAMINE agent is to be used as an aqueous solu- sive rust scale makes it necessary, the interior of the tion (see Physical Properties section). 48 Toxicity and Safety Toxicity Studies Results of acute toxicity testing using DIGLYCOLAMINE agent indicate that this product is slightly toxic by single oral exposure, and practically nontoxic by single dermal exposure. The oral LD50 in rats has been determined to be 2.6 g/ kg, and the dermal LD50 in rabbits is in excess of the 3.0 g/kg maximum concentration employed in our limit test. Acute irritation studies have shown this product to be extremely irritating/corrosive to the skin of rabbits, with a Draize score of 8.0 (maximum score 8.0). Due to its corrosive properties to the skin, rabbit eye irritation studies using DIGLYCOLAMINE agent have not been performed, but it is expected that this product would be extremely irritating/corrosive to the eyes. A dermal sensitization study (Beuhler method) has shown DIGLYCOLAMINE agent to be nonsensitizing to guinea pigs induced and challenged at concentrations of 10% in acetone. A battery of in vitro genetic toxicity studies, employing an Ames assay, a cell transformation assay, and an Unscheduled DNA Synthesis (UDS) assay, did not demonstrate any evidence of DNA damage or cell growth transformation in the test systems. Human Health Effects and First Aid On the basis of the above toxicity studies, the principal health hazard from accidental exposures to DIGLYCOLAMINE agent is a moderate-to-severe irritation/corrosion of the eyes, skin, and mucous membranes. Chemical-type goggles with face shield must be worn during handling or use of the undiluted product or concentrated solutions. Contact lenses should not be worn. Protective clothing and gloves resistant to chemicals and petroleum distillates must be worn. Should accidental eye contact occur, flush eyes with large amounts of water for at least 15 minutes, after which a physician should be consulted. During flushing of the eyes, eyelids should be held apart to permit rinsing of entire surface of eyes and lids. For skin contact, immediately flush skin with large amounts of water for at least 15 minutes. Clothing wet with the product must be removed immediately and laundered before reuse. If DIGLYCOLAMINE agent is accidentally ingested, and the individual is conscious and can swallow, he or she should be given two large glasses of water, after which a physician should be consulted. Since this product is expected to produce severe irritation/corrosion of mucous membranes, vomiting should not be induced, due to the possibility of lung damage from aspiration of the product into the lungs during vomiting. The vapor pressure of DIGLYCOLAMINE agent is quite low, and exposure to harmful quantities of vapor should not be a health problem under usual circumstances. However, adequate ventilation should be provided where a large quantity of product is exposed, or where mists or vapors are generated. Spills in confined areas should be cleaned up promptly. Spill Containment and Disposal Spilled DIGLYCOLAMINE agent can be absorbed using a solid absorbent and placed into drums for disposal. Larger amounts of material may be disposed of by incineration or placement in a properly controlled landfill site. In all instances, disposal of this product should be performed in compliance with all local, state, provincial, and federal regulations. 49 Shipping Information Delivery of DIGLYCOLAMINE agent can be made in 10,000 and 20,000-gallon tank cars. These cars are constructed of welded carbon steel and have bottom unloading fittings and steam coils. Deliveries can also be made in insulated, stainless steel, full or compartmented tank wagons with steam coils. If requested, tank wagons can be equipped with unloading pumps and hoses. Drums of DIGLYCOLAMINE agent can be shipped in truckload or less-than-truckload quantities. The net weight of a drum is 480 pounds; the gross weight is 50 approximately 501 pounds per drum. Drums are UN1A1 or UN1H1, nonreturnable. Under U.S. Department of Transportation (DOT) and Canadian Transportation of Dangerous Goods (TDG) regulations, the proper shipping name for DIGLYCOLAMINE agent is “2-(2-aminoethoxy)ethanol,”identification number UN 3055. This product is considered a corrosive material (TDG hazard class 8) and requires a “CORROSIVE”label for shipping. For further information, please refer to the Material Safety Data Sheet (MSDS) for this product. Bibliography Gas Treating Applications 1. Anon.: “GPA Explores H2S Removal Methods,” Oil & Gas Journal 7 76, No. 29, 66, 71-73 (1978). 2. Barth, D., Tondre, C., and Delpuech, J. J.: “Stopped-Flow Investigations of the Reaction Kinetics of Carbon Dioxide With Some Primary and Secondary Alkanolamines in Aqueous Solutions,” Int. J. Chem. Kinet. 18, No. 4, 445-457 (1986). 3. Bucklin, Robert W.: “DIGLYCOLAMINE (DGA) - A Workhorse for Gas Sweetening,” Oil & Gas Journal 80, No. 45, 204, 208-210 (1982). 4. Butwell, K. F., Kubek, D. J., and Sigmund, P. 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A.: “Equilibrium Data for the Hydrogen SulfideCarbon Dioxide-DIGLYCOLAMINE Agent-Water System,” Proceedings of Annual Convention - Gas Processors Association, 62, 256-268 (1983). 10. Dingman, J. C., and Moore, T. F.: “Compare DGA and MEA Sweetening Methods,” Hydrocarbon Processing 47, No. 7, 138-140 (1968). 11. Drew Chemical Corp.: “Absorption System for Removal of Acidic Gases,” Neth. Appl. 72 13,807, October 12, 1972; C.A. 83 100645w. 51 Bibliography 12. Freireich, E., and Tennyson, R. N.: “Process Improves Acid-Gas Removal, Trims Costs, and Reduces Effluents,” Oil & Gas Journal 74, No. 34, 130-132 (1976). 13. Goar, B. Gene: “Today’s Gas-Treating Processes-1,” Oil & Gas Journal 69, No. 28, 77-79 (1971). 14. Griffith, T. E.: “Gas Sweetening in Field Operations,” Gas 46, No. 5, 77-79 (1970). 15. Harbison, J. L., and Dingman, J. C.: “Mercaptan Removal Experiences in DGA Sweetening of Low Pressure Gas,” Gas Conditioning Conference at the University of Oklahoma, Norman, Oklahoma 1972; C.A. 83 82356w. 16. Hikita, H., Asai, S., Ishikawa, H., and Honda, M.: “The Kinetics of Reactions of Carbon Dioxide With Monoisopropanolamine, DIGLYCOLAMINE, and Ethylenediamine by a Rapid Mixing Method,” The Chem. Eng. J. 14, 27-30 (1977). 17. Hikita, H., Ishikawa, H., Murakami, T., and Ishii, T.: “Densities, Viscosities, and Amine Diffusivities of Aqueous MIPA, DIPA, DGA, and EDA Solutions,” J. Chem. Eng. Jpn. 14, No. 5, 411-413 (1981). 18. Holder, Howard L.: “DIGLYCOLAMINE—A Promising New Acid Gas Remover,” Oil & Gas Journal 64, No.18, 8386 (1966). 19. Huval, M., and Van de Venne, H., “Gas Sweetening in Saudi Arabia in Large DGA Plants,” presented at the March 2-4, 1981, Gas Conditioning Conference at the University of Oklahoma, Norman, Oklahoma. 20. Kohl, Arthur L., and Riesenfeld, Fred C.: Gas Purification, 2nd Ed., Gulf Publishing Co., Houston (1974). 21. Maddox, Robert N., Mains, Gilbert J., and Rahman, Mahmud A.: “Reactions of Carbon Dioxide and Hydrogen Sulfide With Some Alkanolamines,” Ind. Eng. Chem. Res. 26, No. 1, 27-31 (1987). 22. Martin, Joel L., Frederick, D. Otto, and Mather, Alan E.: “Solubility of Hydrogen Sulfide and Carbon Dioxide in a DIGLYCOLAMINE Solution,” Journal of Chemical and Engineering Data 23, No. 2, 163-164 (1978). 23. Mason, J. R., and Griffith, T. E.: “MEA-DGA Switch Saves Steam,” Oil & Gas Journal 67, No. 23, 67-69 (1969). 24. McClure, George: “Removal of Carbon Oxide Sulfide From Liquid Propane,” German Offen. 3,034,386, April 22, 1982; C.A. 97(4):26226f. 52 Physical Properties 25. McClure, George, and Morrow, David C.: “Amine Process Removes COS From Propane Economically:” Oil & Gas Journal 77, No. 27, 106-108 (1979). 26. Moore, T. F., Dingman, J. C., and Johnson, F. L. Jr.: “A Review of Current DIGLYCOLAMINE Agent Gas Treating Applications,” Environ. Prog. 3, No. 3, 207-212 (1984). 27. Peterey, Ernst Q. Jr., and Breland, Clinton D.: “Method and Composition for Fluid Treatment,” U.S. 3,923,954, December 2, 1975; C.A. 84 108273q. 28. Seubert, M. K., and Wallace, G. D. Jr.: “Corrosion in DGA Gas Treating Plants,” presented at NACE Corrosion 85 Meeting, Boston, Massachusetts, March 25-29, 1985. 29. Tennyson, R. N., and Schaaf, R. P.: “Guidelines Can Help Choose Proper Process for Gas Treating Plants,” Oil & Gas Journal 75, No. 2, 78-80, 85-86 (1977). 30. Tonis, Joannes G., and Pienon, Adrianus P.; Shell Internationale Research Maatschappij N.V.: “Washing of Acid Components From Hydrocarbon Gas Streams,” British 1,153,786, May 29, 1969; C.A. 71 32096t. 31. Valdez, Antonio R.; Fluor Corp.: “Separation of Carbon Dioxide, Hydrogen Sulfide, and Moisture From Gaseous Hydrocarbons,” German Offen. 2,451,958, April 30,1975; C.A. 83 118410a. 32. Weber, Steve, and McClure, George: “New Amine Process for FCC Desulfurizes Light Liquid Streams,” Oil & Gas Journal 79, No. 23, 160-161, 163 (1981). 33. Yeakey, Ernest L., and Moss, P. H.; Jefferson Chemical Co., Inc.: “Purifying Gases Containing Acid Impurities Using Stabilized 2-(2-Aminoethoxy) Ethanol,” U.S. 3,891,742, June 24, 1975; C.A. 83 166759t. 34. Yeakey, Ernest L., and Moss, P. H.; Jefferson Chemical Co., Inc.: “Stabilized 2-(2-Aminoethoxy) Ethanol,” U.S. 3,829,494, August 13, 1974; C.A. 81 104738k. 35. Williams, W. W.: “Treatment of Gas Plant Liquids With DIGLYCOLAMINE,’’ Gas Conditioning Conference at the University of Oklahoma, Norman, Oklahoma 1973; C.A. 81 123945s. 53 Bibliography Other Applications 36. Basila, Michael R., and Pate, Alfred R. Jr.; Nalco Chemical Co.: “Extraction of Aromatic Hydrocarbons From Petroleum Hydrocarbons by Using DIGLYCOLAMINE,” S. African 6,905,875, February 26, 1970; C.A. 73 79200d. Corresponds to U.S. 3,583,906 and 3,733,262. 37. Brummet, Berthel D., and Sadler, Fred D.: “Heat Stabilized Paper for Electrical Insulation,” Belgian 667,396, November 16, 1965; C.A. 65 9164b. Corresponds to U.S. 3,403,968 and British 1,060,706. 38. Cooper, Joseph, and Corbett, William J.; W. R. Grace and Co.: “Paint Stripping Compounds,” U.S. 3,417,025, December 17, 1968; C.A. 70 38971a. 39. Eisenlohr, Karl H., and Mueller, Eckart; Metallgesellschaft A.- G.: “Extraction of Aromatic Compounds With Mixed Solvents,” Belgian 670,244, January 19, 1966; C.A. 65 120499. Corresponds to U.S. 3,366,568 and 3,415,739. 40. Frei, Alfred, and Schweizer, August; Sandoz Ltd.: “Stabilized Diazo Dye,” German Offen. 1,929,418, May 21, 1970; C.A. 73 57161q. 41. Globus, Alfred R.: “Stabilization of Ethanol-Gasoline Mixtures,” U.S. 4,328,004, May 4, 1982; C.A. 97(4):26197x. 42. Jones, W. T., and Payne, Vic: “New Solvent to Extract Aromatics,” Hydrocarbon Processing 52, No. 3, 91-92 (1973); C.A. 79 7600k. 43. Markiewitz, Kenneth H.; Atlas Chemical Ind., Inc.: “Urea Compounds for Treating Cellulosic Textiles,” German Offen. 2,058,317, June 3, 1971; C.A. 75 130747h. Corresponds to U.S. 3,763,106 and British 1,305,136. 44. Matsui, Takeshi, and Yashida, Shigeaki; Ricoh Co., Ltd.: “Amine Developers for Diazo Copying Papers,” Japanese 74 20,980, May 29, 1974; C.A. 82 105195p. 45. Murphy, Donald P.; Oxy Metal Ind. Corp.: “Amine Stripping Compounds,” U.S. 3,972,839, August 3, 1976; C.A. 85 144882S. 46. Murphy, Donald P.; Societe Continentale Parker: “Composition for Removing Organic Coatings From Substrates,” French 2,019,526, July 3, 1970; C.A. 74 143414b. Corresponds to U .S. 3,671,465. 54 Physical Properties 47. Neuman, Henry J.: “Amine-Type Developer for Diazo Materials,” U.S. 3,809,560, May 7, 1974; C.A. 81 56643b. 48. Pyrene Co. Ltd.: “Composition and Process for Stripping Paint,” British, 1,229,779, June 29, 1972; C.A. 78 31560x. 49. Sadler, Fred Speer, and Heinrichs, Frank Wheddon; McGraw-Edison Co.: “Impregnating Cellulosic Fibers,” French 2,122,153, September 29, 1972; C.A. 78 112952d. Corresponds to U.S. 3,736,178 and British 1,342,947. 50. Shibe, William J.; R. M. Hollingshead Corp.: “Polyamide Ester Hydraulic Fluids,” U.S. 3,341,543, September 12, 1967; C.A. 67 109252t. 51. Standard Oil Co.: “Lubricants for Metal Machining,” Neth. 65 03,934, September 28, 1965; C.A. 64 7957g. Corresponds to U.S. 3,298,954 and British 1,109,304. 52. Vander Aue, John P.; Goodyear Tire and Rubber Co.: “Polyurethanes,” German Offen. 2,259,955, June 20, 1973; C.A. 79 80091. Corresponds to British 1,365,567. 53. Yashida, Shigeaki, and Matsui, Takeshi; Ricoh Co. Ltd.: “Developer Powder for Binary, Light Sensitive Diazo Papers,” German Offen. 2,126,160, January 27, 1972; C.A. 76 134168p. Corresponds to British 1,357,135. Toxicity 54. Smyth, H. F. Jr., Carpenter, C. P., and Weil, C. S.: AMA Arch. Ind. Hyg. Occup. Med. 4 119 (1951). 55 Sales Office HUNTSMAN CORPORATION 10003 Woodloch Forest Drive The Woodlands, TX 77380 Tel: 281-719-6000 Fax: 281-719-6055 Research and Development Advanced Technology Center 8600 Gosling Rd The Woodlands, TX 77381 Tel: 281-719-7400 Fax: 281-719-7500 Huntsman International Trading Corporation 350 Orchard Road #11-07 Shaw House Singapore 238868 Tel: 65 730-0270 Fax: 65 730-0280 Huntsman International Trading Corporation Taiwan Representative Office 11-F4, 30, Sec. 3 Chung Shan N. Road Taipei, Taiwan R.O.C. Tel: 886-2-2586-3467 Fax: 886-2-8596-1919 Huntsman do Brasil Participacoes, Ltda. 807 Conj. 2314 01311-000 San Paulo - SP, Brazil Tel: 55 11-253-6448 Huntsman Corporation Europe Everslaan, 45 3078 Everberg Belgium Tel: 32-2-758-9211 Fax: 32-2-758-9946 56 Huntsman Corporation Canada Inc. Box 61128 RPO Kensington, Calgary, Alberta, T2N 4S6 Canada Tel: 403-276-1166 Fax: 403-276-1163 Huntsman de Mexico, S.A. de C.V. Angel Urraza Num. 303 Col. 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While all the information presented in this document is believed to be reliable and to represent the best available data on these products, NO GUARANTEE, WARRANTY, OR REPRESENTATION IS MADE, INTENDED, OR IMPLIED AS TO THE CORRECTNESS OR SUFFICIENCY OF ANY INFORMATION, OR AS TO THE SUITABILITY OF ANY CHEMICAL COMPOUNDS FOR ANY PARTICULAR USE, OR THAT ANY CHEMICAL COMPOUNDS OR USE THEREOF ARE NOT SUBJECT TO A CLAIM BY A THIRD PARTY FOR INFRINGEMENT OF ANY PATENT OR OTHER INTELLECTUAL PROPERTY RIGHT. EACH USER SHOULD CONDUCT A SUFFICIENT INVESTIGATION TO ESTABLISH THE SUITABILITY OF ANY PRODUCT FOR ITS INTENDED USE. Products may be toxic and require special precautions in handling. 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