|Publication number||US3355336 A|
|Publication date||Nov 28, 1967|
|Filing date||Aug 18, 1966|
|Priority date||Aug 18, 1966|
|Publication number||US 3355336 A, US 3355336A, US-A-3355336, US3355336 A, US3355336A|
|Inventors||Lyerly William M|
|Original Assignee||Du Pont|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (5), Referenced by (18), Classifications (12)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent ()fiice 3,355,336 Patented Nov. 28, 1967 THICKENED WATER-BEARING INORGANIC OXI- DIZER SALT EXPLOSIVE CONTAINING CROSS- LINKED GALACTGMANNAN AND POLYACRYL- AMlDE William M. Lyerly, Hagerstown, Md, assignor to E. I. du Pont de Nemours and Company, Wilmington, Del., a corporation of Delaware N Drawing. Filed Aug. 18, 1966, Ser. No. 573,206
6 Claims. (Cl. 149-60) ABSTRACT OF THE DISCLQSURE Water-bearing explosives thickened with the combination of crosslinked galactomannan and polyacrylamide.
Background of invention Considerable commercial interest has developed in the use of water-bearing explosives in recent years. Generally, water-bearing explosive compositions comprise an aqueous solution or slurry of inorganic oxidizing salts mixed with organic or metallic fuels and sensitizing agents which can also act as fuels.
While these water-bearing explosive compositions have many inherent advantages such as a wide range of explosive properties, and better safety characteristics and economy, both in manufacture and use, there are likewise many difliculties encountered in their use. Among the major problems encountered in the use of waterbearing-explosive compositions are dilution of the explosive composition by Water which may be present in the borehole and the leaching out of the dissolved and undissolved, but water-soluble, oxidizing salts thus leading to changes in composition which result in losses in explosive power or even in failures to detonate. In addition, even in dry boreholes segregation of components can take place under certain conditions so that solid components separate into layers above or below the aqueous salt solutions to the extent that gross inhomogeneity occurs, again leading to loss of strength and failure to propagate. Many attempts have been made in the art to overcome the aforementioned difficulties.
Galactomannans, particularly guar gum, have found wide utility as thickening or gelling agents in improving the water-resistance of water-bearing explosives. However, if the galactomannans are not highly crosslinked, such products gradually segregate and do not meet the stringent water-resistance requirements of current commercial explosives. On the other hand, guar compositions sufficiently cross-linked for good water-resistance yield relatively immobile gelled masses which, in some cases, are disadvantageous and difficult to handle and load into boreholes. For example, stiff, non-pourable gels tend to spread and plug boreholes partially filled with water when they strike the surface of the water. Also, such compositions are somewhat more inconvenient to remove from containers than more pourable products and do not spread to fill the available space in the borehole leaving voids which could prevent propagation of detonation. The foregoing problems become progressively greater as the diameter of the borehole is reduced.
Substantially linear, water-soluble or water-dispersible vinyl polymers also have been proposed to gel or thicken Water-bearing explosives. However, unless these polymers are crosslinked, as in U.S.P. 3,097,120, or are present in high concentration, they give very little body to the explosives. Furthermore, such polymers are relatively expensive.
Summary of invention and preferred embodiments This invention provides thickened water-bearing explosives which do not segregate and are water resistant over a wide range of viscosities. Preferred compositions of this invention have a unique combination of pourability and fluidity coupled with resistance to water and segregation which makes them particularly suitable in small diameter holes and in holes partially filled with water.
Accordingly, this invention provides water-bearing explosive compositions comprising inorganic oxidizing salt, fuel and water, which improvement comprises thickening said compositions with the combination of polyacrylamide and crosslinked galactomannan, the weight ratio of said polyacrylamide to galactomannan being from about 0.1:1 to 10:1, and preferably 1:1 to 5:1. Thickened as used herein refers to compositions in which the viscosity of the aqueous phase has been increased, e.g., to 10,000 centipoises or more, as well as to gelled products, including those gels which are crosslinked.
The polyacrylamide used is a preformed polymer which has a molecular weight of 1 to 25, and especially 3 to 15 million. Molecular weight can be determined from the relation:
wherein V is the intrinsic viscosity of the polymer in dl./ grams and M.W. is its molecular weight. Intrinsic viscosity can be determined in the conventional manner from inherent viscosity measured in dilute solutions in water at 30 C. with an Ostwald Fenske viscometer. Preferred polymers have a pH as a 1% by weight solution in water at 30 C. of about from 6 to 8, and preferably 6.5 to 7.5. Preferably, the polymer contains at least 10% by weight of carboxylate (-COO) moieties neutralized with alkali, alkaline earth metal or ammonium bases.
Galactaomannans which can be used in this invention include, e.g., guar gum and locust bean gum, and also other galactomannan gums which include those from endosperm seeds of leguminous plants such as the sennas, brazilwood, tara, honey locust, paloverde, rattle'box, alfalfa gum, clover gum and fenugreek gum. Of these, guar gum is particularly preferred because of its ready availability, stability and general compatibility with aqueous solutions of inorganic oxidizing agents.
The galactomannans are crosslinked in the aqueous solution of the inorganic oxidizing salt to form stable gelled products at relatively low concentrations of preformed polyacrylamide and galactomannan and to impart greater strength, cohesiveness and water-resistance to the resulting compositions. Any of the known crosslinking agents conventionally employed for galactomannans can be used including potassium and sodium dichromate; sodium tetraborate as described in U.S.P. 3,072,509; soluble antimony and bismuth compounds at a pH of from about 6 to 13 as in U.S.P. 3,202,556; and transition metal compounds as in S.N. 343,140, filed Feb. 6, 1964, the teachings of each of which is included herein by reference. Systems, especially those comprising soluble antimony and bismuth compounds plus oxidizing agents are preferred for forming water-resistant, pourable compositions. The terms soluble antimony and bismuth compounds as used herein refer to antimony or bismuth in ionic form, preferably as Sb+ Bi SbO+ or BiO+ or a combination thereof, in the gelation system, for example, in aqueous or aqueous nitrate containing solutions of galactomannan gum during the gelation reaction. In general, the foregoing is fulfilled by antimony or bismuth compounds soluble to the extent of at least about 1 part per million in the gelation system. Examples of antimony or bismuth compounds which can be used in the process of this invention include oxides and organic and inorganic salts of bismuth and antimony such as antimony oxide, antimony chloride and antimony oxychloride, antimony sulfate, antimonyl sulfate, antimony tartrate, potassium antimonyl tartrate, sodium pyroantimonate, antimony fluoride, antimony citrate, bismuth oxide, bismuth chloride, bismuth citrate, sodium bismuthate, bismuth nitrate and mixtures thereof. Alkali metal antimony salts of hydroxylate polybasic acids, particularly potassium antimony tartrate, are preferred. Oxidizing agents used in combination with the above include hydrogen peroxide, alkali and alkaline earth peroxides, and alkali, alkaline earth and ammonium permanganates, chromates and dichromates. However, alkali metal dichromates, e.g., sodium and potassium dichromates are especially preferred.
In the process of this invention the particularly preferred crosslinking agent is potassium antimony tartrate and the particularly preferred oxidizing agent is alkali metal, especially sodium or potassium dichromate. The concentration of antimony or bismuth crosslinking agent based on the amount of galactomannan is about from 1 to 15%, preferably 2 to by weight of potassium antimony tartrate or an equivalent and about from 0.2 to 5% preferably 0.5 to 3% by weight of potassium dichromate.
The rate of gelatin and final viscosity of the gelled compositions of this invention is related to the kind and concentration of the galactomannan, the molecular weight and concentration of the preformed polyacrylamide, and the kind and concentration of the crosslinking agent. Thus, it will be apparent that the variables are interrelated and conveniently are adjustable to provide a gel having the desired properties during manufacture, storage, shipping and use. As indicated earlier, a particularly preferred composition of this invention is a pourable, water-resistant, Water-bearing explosive composition containing a ratio of polyacrylamide to guar gum of about from 1/1 to 5/l, most preferably 2/1 to 3/1, the total amount of guar gum and polyacrylamide employed being less than about 2%, and preferably less than 1%, by weight of the total explosive composition. The crosslinking agent, used in the quantities set forth above, will react with the guar gum to form a gel in the aqueous phase of the blasting composition, the polyacrylamide functioning primarily as a thickening agent. Thicker, i.e., more viscous, less pourable compositions can be obtained by employing a larger weight percentage of galactomannan (guar) and/or polyacrylamide, by employing a higher ratio of crosslinking agent to galactomannan, by using polyacrylamide of higher molecular Weight, and/or by providing a crosslinking system which will provide a more highly crosslinked, stable structure with the galactomannan.
In its broad aspects the improvement of this invention can be applied to any of the known general types of water-bearing explosives fluid at room temperature having a continuous phase comprising water. The compositions of this invention usually contain at least about 20% by weight of an inorganic oxidizing salt. Such salts include ammonium, alkali metal and alkaline earth metal nitrates and perchlorates as well as mixtures of two or more of such salts. Examples of such salts are ammonium nitrate, ammonium perchlorate, sodium nitrate, sodium perchlorate, potassium nitrate, potassium perchlorate, magnesium nitrate, magnesium perchlorate and calcium nitrate. Preferably, the inorganic oxidizing salt component contains at least 45% of at least one salt which is highly soluble in water at room temperature, that is, at least as soluble as ammonium nitrate, and preferably, the aqueous phase in the composition contains a substantial portion of oxidizing salt, for example, 40 to 70% by weight thereof. Inorganic oxidizing salt mixtures containing at least about 50% by weight of ammonium nitrate and at least about 50% by weight of sodium nitrate are particularly preferred.
The fuels employed in the compositions of this invention can be, for example, self-explosive fuels, non-explosive carbonaceous and metallic fuels, or mixtures of the aforementioned types of fuels. The fuel or fuels used in the compositions of this invention can be varied widely,
provided that in the composition in which any particular fuel is used, the fuel is stable, that is, prior to detonation, during preparation and storage, the fuel is chemically inert with the system. Selfexplosive fuel as used herein refers to a substance which by itself is generally recog nized in the art as an explosive. Examples of selfexplosive fuels include organic nitrates, nitro compounds, and nitramines such as TNT, pentaerythritol tetranitrate (PETN), cyclotrimethylenetrinitramine (RDX), cyclotetramethylenetetranitramine (HMX), tetryl, nitrostarch, explosive-grade nitrocellulose and smokeless powder, as Well as mixtures of the aforementioned self-explosive fuels such as, for example, pentolite (PETN/TNT), Composition B RDX/TNT) and tetratol (tetryl/TNT). The selfexplosive fuel can be, for example, in any of the conventional flake, pelleted or crystalline forms. The amount of fuel varies with the particular fuel employed. In general. up to 40 and, preferably, 10 to 40% by weight based on the weight of composition of self-explosive fuel is used.
Examples of carbonaceous non-explosive fuels include finely-divided coal and other forms of finely divided carbon; solid carbonaceous vegetable product such as cornstarch, woodpulp, sugar, ivory nut meal and bagasse; organic liquids such as hydrocarbon oils, fatty oils and vegetable oils; urea; and mixtures of two or more of the aforementioned carbonaceous fuels are employed.
Metallic fuels include, for example, aluminum and iron, and alloys of such metals such as aluminum-magnesium alloys, ferrosilicon, ferrophosphorus, as well as mixtures of the aforementioned metals and alloys. Although, as disclosed in U.S. Patent 2,836,484, up to about 50% by Weight of metallic fuel can be employed in water-bearing compositions, usually on the order of 1 to 20, and preferably l to 8% by Weight of metals such as aluminum, and on the order of about 10 to 30% by weight of heavier metallic fuels such as ferrophosphorus and ferrosilicon are employed.
Preferably, the total amount of fuel is adjusted so that the total composition has an oxygen balance of about from -30 to +10% and, excepting for those compositions containing the aforementioned heavier metallic fuels such as ferrophosphorus and ferrosilicon, preferably the oxygen balance is between about 15 to 0%.
To further enhance fluidity of the compositions of this invention, particularly at low temperatures, they can contain 0.25 to 10%, and preferably 1 to 5%, based on the total weight of composition of fluidizing agent as described in US. Patent 3,190,777, which is incorporated herein by reference. Preferred fluidizing agents include dimethyl sulfoxide, methanol, formamide and methyl cellosolve.
As previously indicated, the compositions of this invention contain at least about 5% by weight of water. The water-bearing compositions to which this invention is directed generally contain less than about 45% by weight of water and, preferably on the order of about 10 to 30% by weight of water based on the total composition.
In general, the explosive compositions of this invention can be prepared by the conventional formulating techniques used for preparing galactomannan or crosslinked galactomannan aqueous explosives. Preferably, however, the galactomannan, mixed with soda, preformed polyacrylamide and fuels is added to a hot (200 F.) concentrated solution containing the major proportion of oxidizing salt, then the crosslinking agents are added, the solution is mixed and the product packed. It has been found particularly advantageous for improved uniform dispersion to add approximately one-third of the ammonium nitrate liquor first, then to add the remaining ingredients, and finally, after about 30 seconds, add the balance of the ammonium nitrate liquor.
This invention provides a means for making waterbearing explosive compositions having excellent waterresistance in products varying in characteristics from pourable fluids to moldable, tough plastic masses. The compositions of this invention have excellent cohesiveness over a wide range of viscosities. Furthermore, the improvement of this invention alters the crystal growth of inorganic salts, reduces crystal size, and improves sensitivity. When measured at 25 C. in the aqueous phase without solids, the preferred fluid compositions have a viscosity of about from 100,000 to about 400,000 centipoises, preferably 150,000 to 300,000 centipoises, as measured on a Brookfield Synchrolectric viscometer, Model RVT with a helipath attachment using a TC spindle at 1 rpm. These fluid compositions are particularly outstanding in their ease of packing and loading and the facility with which they fill boreholes yet resist segregation, leaching and dilution in the presence of water. Such fluid products are also eminently suited for rapid loading in small diameter holes giving ease in borehole loading which has heretofore only been obtainable with products blended in situ at the blasting site, e.g., in slurry trucks, but economically infeasible for use in smaller blasting operations.
As previously indicated, the explosive compositions of this invention can vary from pourable fluids to moldable, tough plastic masses, all having excellent water-resistance and excellent cohesiveness. Particularly preferred compositions of this invention are pourable explosive compositions having a viscosity of 150,000 to 300,000 centipoises, and containing, by weight, 20 to 60% ammonium nitrate alone or in combination with to 40% sodium nitrate; to 40% fuel, preferably TNT; 10 to 30% Water; 0.1 to 0.5% guar gum; 0.2 to 1.0% preformed polyacrylamide; and, based on the weight of galactomannan, about from 0.5 to 3% of oxidizing agent, preferably an alkali metal dichromate such as sodium or potassium dichromate and 2 to 10% of an antimony compound soluble in the system, preferably potassium antimony tartrate.
The compositions of this invention possess greater fluidity, homogeneity, resistance to disintegration or leaching by water and stability, i.e., resistance to degradation and settling out of components, than compositions which contain only substantially linear, water-soluble or water-dispersible vinyl polymers or those which contain only crosslinked galactomannans. This greater fluidity, homogeneity, stability and water-resistance is particularly advantageous when the compositions are to be used in wet locations, since disintegration and leaching of a composition by water, if such occurs, can lead to failures to detonate or to propagate a detonation throughout the length of an explosive column. If the explosive structure degrades, i.e., by virtue of disintegration of the gel structure, subsequent segregation of components, particularly undissolved (solid) fuels and sensitizers, can occur under the force of gravity, and the components in a borehole, whether in a container or cartridge, shucked therefrom, or simply poured into a borehole will 'become so heterogeneous that complete failure of detonation or propagation of detonation through the entire length of the column of the explosive charge will occur. Further, the compositions can be packaged in containers compatible with the ammonium nitrate liquor employed, e.g., of polymeric materials, and stored until time of use without deterioration or separation of components. Even when freed from the container these compositions retain an optimum degree of resistance to disintegration and leaching by water which may be already present in the borehole or which may enter the borehole after the compositions are loaded. With the compositions of this invention, bottom of the hole loading is not required. Likewise, the material will not block a borehole as a conventional water gel very often does. The higher loading per foot of borehole and speed of loading compared to either cartridged products or normal water gels are significant advantages which are manifest in the compositions of this invention.
In the following examples which illustrate this invention parts, percentages and ratios are by weight unless otherwise indicated.
Examples 1 to 5 Water-bearing explosive compositions of this invention are prepared from the materials noted in Table I. The formulations are prepared in a rotary mixer in the following sequence of steps:
(1) One-third of 65% ammonium nitrate solution at ISO- F., is placed in the mixer, and to the ammonium nitrate solution, with continuous agitation, is added 6 to 8 mesh pelleted TNT or smokeless powder, hydrocarbon oil (C0rvus oil), metal fuels and/ or sulfur as indicated in the table.
(2) A premixed composition of sodium nitrate, polyacrylamide and galactomannan is added and the contents of the resulting mixture are agitated for 15 seconds.
(3) The balance of the ammonium nitrate liquor and formamide, where used, are added and the contents of the mixture are agitated for 3 minutes.
(4) The oxidizing agent is added and incorporated in the blend by agitating for 15 seconds.
(5) Crosslinking agent is added and the blend is mixed 30 seconds more.
(6) Contents of mixer are discharged into polyethylene bags.
TABLE I Example 1 2 3 4 5 65% AN liquor 50 57 5D 42 30 Ammonium Nitrate.-- 37 20 Water Sodium Nitrate TNT Smokeless Powder Aluminum Ferrophosphorus Sulfur The compositions also contain per hundred weight:
Corvus oil, lbs 0. Formarnide 2 Guar gum, lbs 0. Polyacrylamide, lbs... 0. 5% Solution, KzC1207,
cc 5% PAT, 2 cc Velocity, m./sec.,
B 4, 200 Density, g./cc 1. 4 1. 5 4 1. 65
1 Molecular wt., 5-6 million; pH of 1% solution in Hz0-7; neutralized carboxylate 10%.
1 Potassium antimony tartrate.
3 Tested in 23-inch diameters in air.
4 Tested in 4-inch diameters in air.
5 Tested in 5-inch diameters in air.
In Examples 1 to 4, the finished compositions are pourable, water-resistant gels having a density of from about 1.45 to about 1.65 g./cc. and a pH of about 7 to 9. The viscosity of the compositions is from about 100,000 to 400,000 cps. The composition in Example 5 is a stiff water-gel suitable for use in mudcapping; operations. All the compositions in Table I are uniform in appearance and composition, and undissolved components remain uniformly dispersed. Even when the compositions are dropped approximately 40 or more feet into water, no evidence of breakdown of the gel structure is noted. No evidence of incompatability with water-filled boreholes is found. Deliberate attempts to plug a borehole with compositions of Examples 1 to 4 are not successful. The formulations in Examples 1 to 4 will flow through a 1- inch-diameter funnel at 70 F and have suflicient waterresistance whereby bottom of the hole loading is not required. The compositions are not cap-sensitive but can be detonated by a conventional 25 g. RDX primer and detonate with a velocity of about 4100 meters/second in a Z-inch-diameter column.
In the foregoing examples, similar results are obtained when a bismuth compound or a transition metal comdeteriorate in 12 weeks or more of storage at 20 F. or
TABLE II Composition, percent by wt.
Composition, per hundred Weight Example I Time for No. 1 i i i Deterioration 65% A I TNT Sodium Formamide, Guar Gum, Iolvatryl- (.orvus" PAT, K2CI2O7, 7 Liquor Nitrate lbs. lbs. 1 amide. ibs. nil, lbs. cc. cc.
50.0 i 30.0 20.0 1 3.0 J 0.0 l 0.25 i 80.0 i 25.0 i 5Weeks 57.0 25.0 18.0 3.0 0.75 Q 0.25 .n 10.0i1lhours 57.0 25. 18. 0 3. 0 35 i o 0. 25 i 100. 0 i 25.0 1.2 weeks 57.0 25.0 i 13. 0 i 3.0 0.6 l 0.3 0.25 7 100.0 25.0 Do. 57.0 25.0 18.0 i 3.0 l 0.27 F 0.8 i 0.25 100.0 25.0 Do.
i l i 1 I 1 pound, especially Tyzor LA, is employed in place of 5 I claim:
the potassium antimony tartrate as the crosslinking agent for the galactomannan.
available from E. I. du Pont de Nemours & Company.
Examples 6-10 In order to evaluate the stability of the gelled waterbearing explosive compositions of this invention and to compare them with compositions containing only polyacrylamide or only guar gum, a sample of each composition, described in Table II, and prepared by the general procedure of Examples 1 to 5 is placed in a tightly closed glass container in a chamber maintained at F. The composition in Example 7 which contains only guar gum becomes hard at this temperature, is not pourable, and separation of the ingredients occurs in a matter of hours. All the other compositions are pourable, water-resistant compositions at this temperature. About four weeks later, the compositions in Examples 6, 8, 9, and 10, which are still pourable, coherent, water-resistant gels, are transferred to a chamber maintained at 100 F. This is representative of a moderately high temperature which might be experienced in a field storage magazine or a service truck. The compositions stored at 100 F. are inspected at intervals for evidence of deterioration such as obvious softening and slumping of gel structure, visible segregation of liquid (syneresis) or insoluble high density material such as TNT, foaming and development of tackiness and stickiness in compositions which were originally pourable, water-resistant gels. As illustrated in Table II, the composition in Example 6 which contains only polyacrylamide has started to deteriorate whereas compositions of the instant invention containing a combination of polyacrylamide and guar gum do not break down or noticeably l Titauiumantimonium lactate chelate.
1. In thickened water-bearing explosives comprising inorganic oxidizing salt, fuel, water and thickening agent, the improvement which comprises using as the thickening agent the combination of cross-linked galactomannan and polyacrylamide, the Weight ratio of said polyacrylamide to galactomannan being about from 0.121 to 10:1, the resulting explosive being water-resistant and non-segregating yet pourable.
2. A pourable composition of claim 1 wherein said galactomannan is guar gum, the weight ratio of polyacrylamide to guar being about from 1:1 to 5:1.
3. A composition of claim 2 wherein the aqueous phase has a viscosity of about from 100,000 to 400,000 cps. at room temperature.
4. A composition of claim 3 crosslinked with the combination of a soluble antimony compound and oxidizing agent.
5. A composition of claim 4 crosslinked with the combination of potassium antimony tartrate and alkali metal dichromate.
6. A composition of claim 1 comprising, by weight based on the total composition, about from 20 to of ammonium nitrate, about from 10 to 40% of sodium nitrate, about from 15 to 40% of fuel, about from 10 to 30% of water, about from 0.1 to 0.5% of guar gum and about 0.2 to 1% of polyacrylamide, said composition being crosslinked with, based on the weight of the guar, about from 0.5 to 3% of alkali metal dichromate and 2 to 10% of potassium antimony tartrate, said polyacrylamide having a molecular weight of about from 3 to 15 million and a pH in a 1% by weight solution in water of about from 6 to 8.
References Cited UNITED STATES PATENTS CARL D. QUARFORTH, Primary Examiner. BENJAMIN R. PADGETT, Examiner.
S. J. LECHERT, JR., Assistant Examiner.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3097120 *||Aug 11, 1961||Jul 9, 1963||American Cyanamid Co||Gelled ammonium nitrate explosive containing polyacrylamide and an inorganic cross-linking agent|
|US3097121 *||Aug 11, 1961||Jul 9, 1963||American Cyanamid Co||Powdered ammonium nitrate explosive containing polyacrylamide and an inorganic cross-linking agent|
|US3190777 *||May 1, 1963||Jun 22, 1965||Du Pont||Fluidizing agents for water-bearing explosive compositions|
|US3202556 *||Jul 23, 1963||Aug 24, 1965||Du Pont||Method for gelling water-bearing explosive compositions containing galactomannan gums|
|US3341383 *||Aug 12, 1966||Sep 12, 1967||Stein Hall & Co Inc||Aqueous ammonium nitrate explosive slurries containing partially hydrolyzed acrylamide polymer|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3442729 *||Dec 28, 1967||May 6, 1969||Hercules Inc||Aqueous inorganic oxidizer salt explosives and acrylamide polymers as thickener therefor|
|US3445305 *||Jun 2, 1967||May 20, 1969||Du Pont||Gelation of galactomannan containing water-bearing explosives|
|US3446681 *||Apr 18, 1968||May 27, 1969||Dow Chemical Co||Gelled slurry explosive composition containing a terpolymer gelling agent|
|US3451868 *||May 4, 1967||Jun 24, 1969||Du Pont||Water-bearing explosive compositions gelled with polymeric amide-aldehyde and method of making same|
|US3457128 *||Feb 13, 1968||Jul 22, 1969||Commercial Solvents Corp||Safe aqueous slurries of particulate nitrated explosives and polyacrylamides|
|US3465675 *||Oct 11, 1967||Sep 9, 1969||Commercial Solvents Corp||Process of blasting with thickened slurried inorganic oxidizer salt-alcohol water explosive mixtures|
|US3475238 *||Feb 14, 1968||Oct 28, 1969||Dow Chemical Co||Method for preparing gelled slurry explosive compositions containing distinct liquid and solid phases|
|US3622408 *||Nov 15, 1967||Nov 23, 1971||Du Pont||Water-bearing explosives thickened with a partially hydrolyzed acrylamide polymer|
|US7244440||Jun 8, 2004||Jul 17, 2007||Alcon, Inc.||Ophthalmic compositions containing a synergistic combination of three polymers|
|US7306802||Jun 4, 2007||Dec 11, 2007||Alcon, Inc.||Ophthalmic compositions containing a synergistic combination of three polymers|
|US7329411||Jun 4, 2007||Feb 12, 2008||Alcon, Inc.||Ophthalmic compositions containing a synergistic combination of three polymers|
|US7618620||Oct 18, 2007||Nov 17, 2009||Alcon, Inc.||Ophthalmic compositions containing a synergistic combination of three polymers|
|US7709012||Jun 8, 2004||May 4, 2010||Alcon, Inc.||Ophthalmic compositions containing a synergistic combination of two polymers|
|US7914803||Feb 9, 2007||Mar 29, 2011||Alcon, Inc.||Ophthalmic compositions containing a synergistic combination of three polymers|
|US7947295||Feb 9, 2007||May 24, 2011||Alcon, Inc.||Ophthalmic compositions containing a synergistic combination of two polymers|
|US8313754||Apr 11, 2011||Nov 20, 2012||Novartis Ag||Ophthalmic compositions containing a synergistic combination of two polymers|
|US20040253202 *||Jun 8, 2004||Dec 16, 2004||Alcon, Inc.||Ophthalmic compositions containing a synergistic combination of three polymers|
|US20040253280 *||Jun 8, 2004||Dec 16, 2004||Alcon, Inc.||Ophthalmic compositions containing a synergistic combination of two polymers|
|U.S. Classification||149/60, 149/76, 149/32, 149/83, 149/44, 149/41, 149/61, 149/85|
|International Classification||C06B47/00, C06B47/14|