US3534906A - Control of atmospheric particles - Google Patents
Control of atmospheric particles Download PDFInfo
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- US3534906A US3534906A US684550A US3534906DA US3534906A US 3534906 A US3534906 A US 3534906A US 684550 A US684550 A US 684550A US 3534906D A US3534906D A US 3534906DA US 3534906 A US3534906 A US 3534906A
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- particles
- polyelectrolyte
- fog
- cloud
- atmospheric
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Links
- 239000002245 particle Substances 0.000 title description 38
- 229920000867 polyelectrolyte Polymers 0.000 description 25
- 238000000034 method Methods 0.000 description 17
- 229920002873 Polyethylenimine Polymers 0.000 description 10
- 238000001556 precipitation Methods 0.000 description 10
- 230000008569 process Effects 0.000 description 10
- 239000000779 smoke Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 239000007921 spray Substances 0.000 description 9
- 238000005507 spraying Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 6
- 238000004581 coalescence Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000002776 aggregation Effects 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 238000010899 nucleation Methods 0.000 description 4
- 238000005054 agglomeration Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000003595 mist Substances 0.000 description 3
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000000280 densification Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229940047670 sodium acrylate Drugs 0.000 description 2
- 229940006186 sodium polystyrene sulfonate Drugs 0.000 description 2
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 229910021612 Silver iodide Inorganic materials 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229920001448 anionic polyelectrolyte Polymers 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003467 diminishing effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 239000005486 organic electrolyte Substances 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical group [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E01—CONSTRUCTION OF ROADS, RAILWAYS, OR BRIDGES
- E01H—STREET CLEANING; CLEANING OF PERMANENT WAYS; CLEANING BEACHES; DISPERSING OR PREVENTING FOG IN GENERAL CLEANING STREET OR RAILWAY FURNITURE OR TUNNEL WALLS
- E01H13/00—Dispersing or preventing fog in general, e.g. on roads, on airfields
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01G—HORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
- A01G15/00—Devices or methods for influencing weather conditions
Definitions
- a further object is to provide a means whereby fog may be quickly and safely abated.
- a still further object is to provide an improved method for the modification of clouds to alter their physical form and moisture content.
- a still further object is to provide a method whereby smoke, smog and the like may be substantially removed from the air thereby diminishing air pollution.
- a polyelectrolyte in fine particulate form is contacted with the fog, smoke, cloud or other atmospheric mass of particles to be modified.
- the presence of the polyelectrolyte ena'bles the water droplets or other particles in the fog, cloud or atmosphere to coalesce by altering the electrostatic charge on such droplets.
- Such coalescence is therefore produced wtihout dependence on the surrounding temperature thereof being below the freezing point of water.
- Suitable polyelectrolytes for use in the process of this invention may be cationic, anionic, nonionic or amphoteric, hydrophobic or hydrophylic and include polyalkylenimines such as polyethylenimine or polypropylenimine, polyalkylenepolyamines such as the condensation polymers of diethylenetriamine and dihaloalkanes, sodium polystyrene sulfonate, copolymers of sodium acrylate and acrylamide, partially hydrolyzed, crosslinked, polyacrylamides such as are defined in US. Pat.
- the organic polyelectrolytes must have a molecular Weight of at least 30,000 and preferably of at least 50,000.
- Such polyelectrolytes may be employed either in aqueous solution, spray or mist form or in the form of a finely-divided particulate solid.
- the most effective size of the particles of polyelectrolyte or polyelectrolyte solution is from about 10 microns to about 50 mesh (Standard sieve size). Particles smaller than 10 microns lose effectiveness in producing coalescence of the atmospheric particles and particles larger than 50 mesh, while effective, begin to significantly reduce the number of particles produced from a given volume of polyelectrolyte and therefore become ineificient.
- the coagulation and precipitation of the water particles herein is electrostatically produced, it is necessary that at least a portion of the polyelectrolyte employed contains a different charge from that of the fog or cloud to be treated. Therefore, since clouds and fogs usually have an electronegative charge, it is often desirable to employ a cationic electrolyte, or where the fog, cloud, or other particulate mass to be coagulated and dispersed contains a positive charge, an anionic polyelectrolyte may be employed. However, aggregation and precipitation of particles is also accomplished by the addition of a polyelectrolyte of similar charge but of different magnitude and which, therefore, disrupts the electrostatic equilibrium.
- the amount of polyelectrolyte or polyelectrolyte solution required for a given atmospheric condition will vary depending upon the density of the atmospheric particles, e.g., the density of the cloud or fog, the depth of the mass of atmospheric particles through which it is to pass, and the like.
- density of the atmospheric particles e.g., the density of the cloud or fog
- depth of the mass of atmospheric particles through which it is to pass e.g., the density of the cloud or fog
- the depth of the mass of atmospheric particles through which it is to pass e.g., the density of the cloud or fog, the depth of the mass of atmospheric particles through which it is to pass, and the like.
- differently charged particles combine to form a particle of altered electrical charge which falls through the atmospheric mass, collides with other particles to produce a large particle and continues to increase in acceleration and speed until the surface tension is overcome and the particle redivides.
- Each of the divided particles then continues to fall and grow to produce a chain-reaction of acceleration and division of particles.
- Any suitable means may be employer to distribute the polyelectrolyte within the fog, smoke, cloud, or other particle-containing atmospheric mass and thereby produce contact between the dissimilar particles, i.e., the atmospheric particles and the polyelectrolyte particles.
- spraying a solution of the polyelectrolyte above or within the fog or cloud from an airplane or helicopter, explosively dissiminating the polyelectrolyte within the cloud by means of a bomb or exploding rocket, spraying or blowing the polyelectrolyte from ground vehicles, and the like produces sufiicient dispersion to cause coalescence and precipitation of the particles and thereby produce dissipation of fog or smoke and rain, snow or other precipitation from clouds.
- EXAMPLE 1 Steam was injected into a room 20 ft. x 12 ft. x 8 ft. until a dense fog was produced. The degree of fog density was measured by shining a light a distance of 16 feet through the fog and into a light intensity meter such that higher readings are produced on the light intensity with less dense fog and lower readings with more dense fog. A reading of 120 units is achieved when no fog is present.
- EXAMPLE 2 In the same manner as Example 1, a weight percent solution of polyethylenpolyamine (Purifloc C-31) having a molecular weight of about 100,000 was sprayed four feet above the beam of light for a period of five seconds at a rate of one gram of spray per second. After 30 seconds from the beginning of application of the spray, the light intensity meter reading had increased to 20 units and remained at this value for a period of one minute. After a total of three minutes, the intensity meter reading had returned to the equilibrium value of 18 units.
- Purifloc C-31 polyethylenpolyamine having a molecular weight of about 100,000
- EXAMPLE 3 In the manner of Example 1, a weight percent aqueous solution of polyethylenimine having a molecular weight of about 100,000 was sprayed for two minutes along a line four feet above the light beam. During this period the light intensity meter reading rose to a value of 24 units and an additional three minutes was required for the reading to return to the equilibrium value of 18.
- EXAMPLE 4 In order to demonstrate the applicability of the process of this invention to disperse a warm fog from airport runways under actual field conditions, an experiment was conducted at a large airport in the southern United States. For purposes of the test both a transmissometer and ground observers were employed to determine the effect of the test on visibility. The test was begun at 7:05 am. with an initial visibility of feet to feet with no runway lights visible to the observers. An aircraft was flown over one runway at an altitude of about 500 feet and a 5% solution of polyethylenimine having a molecular weight of about 100,000 was applied at the rate of 200 lbs./ sq. mile in seven passes over the runway. Both transmissometer readings and ground visual observers recorded that visibility rapidly increased with each pass of the spraying operation and by 8:00 am. after six of the seven passes had been completed, visibility had increase to 3200 feet.
- EXAMPLE 5 A heavily forested area covered by a large cloud of ascending white-grey smoke from burning saw mill waste was treated with a 5 weight percent aqueous solution of polyethylenimine by spraying a mist of such solution from an airplane just above the smoke (an altitude of about 100 feet). As the polyelectrolyte solution passed into the smoke a definite color change to blue was observed, showing densification of the smake and the color change and densification could be seen continuing down through the rising smoke. After a second application of polyelectrolyte, the forest could be seen through the treated portion of the smoke but was not visibile through the untreated portions.
- a process for the control of particles suspended in the atmosphere which comprises contacting a mass of suspended atmospheric particles with an organic polyelectrolyte having a molecular weight of at least 30,000 in fine particulate form to modify the electrical charge of said atmospheric particles thereby to produce coalescence and precipitation of such particles.
Description
United States Patent 3,534,906 CONTROL OF ATMOSPHERIC PARTICLES Jay Don Gensler, Alexandria, Va., assignor to The Dow' Chemical Company, Midland, Mich., a corporation of Delaware No Drawing. Filed Nov. 20, 1967, Ser. No. 684,550 Int. Cl. Atllg 15/00 US. Cl. 239-2 9 Claims ABSTRACT OF THE DISCLOSURE This invention relates to a method for the control of atmospheric moisture and more particularly relates to a method for fog abatement and the modification of clouds.
In the past, many methods have been proposed to modify clouds to produce rain or snow, to dissipate haze or fog, to modify and decrease the intensity of tropical storms or hurricanes, or to remove smoke, smog and the like from the air. Most of the reported work in the area deals with cloud modification and many materials have been employed with varying degrees of success. In general, to produce rain from a cloud by seeding, it is necessary to employ an ice-former such as silver iodide or Dry Ice or a hygroscopic material such as NaCl, CaCl MgCl and the like. Usually such seeding materials depend on a temperature within the cloud of less than 0 C. so that ice crystals form and grow. Many low clouds, fogs and the like are too warm, however, and such seeding materials are not elfective. Attempts have been made to produce rain from low warm clouds and fog by employing hygroscopic materials or sprays of water thereto to etfect coalescence and precipitation of the particles within the cloud. While rain has at times been produced by this method, such rainfall will not propagate. itself unless the cloud was already in a metastable condition. Another problem presented in present systems is that very thick layers of cloud or fog, e.g., 5000 ft., are normally required to achieve good nucleation, coagulation and precipitation. Therefore, while a process to reliably control the agglomeration of atmospheric particles is greatly de sired, no method has been heretofore provided which is effective in producing the agglomeration and subsequent precipitation of particles suspended in the air, particularly when such particles are above the freezing point.
It is an object of this invention to provide a means for controlling atmospheric particles by producing agglomeration and precipitation thereof. A further object is to provide a means whereby fog may be quickly and safely abated. A still further object is to provide an improved method for the modification of clouds to alter their physical form and moisture content. A still further object is to provide a method whereby smoke, smog and the like may be substantially removed from the air thereby diminishing air pollution. These and other objects and advantages of the present invention will become obvious from a reading of the following detailed description.
In accordance with the process of this invention, a polyelectrolyte in fine particulate form is contacted with the fog, smoke, cloud or other atmospheric mass of particles to be modified. The presence of the polyelectrolyte ena'bles the water droplets or other particles in the fog, cloud or atmosphere to coalesce by altering the electrostatic charge on such droplets. Such coalescence is therefore produced wtihout dependence on the surrounding temperature thereof being below the freezing point of water.
Suitable polyelectrolytes for use in the process of this invention may be cationic, anionic, nonionic or amphoteric, hydrophobic or hydrophylic and include polyalkylenimines such as polyethylenimine or polypropylenimine, polyalkylenepolyamines such as the condensation polymers of diethylenetriamine and dihaloalkanes, sodium polystyrene sulfonate, copolymers of sodium acrylate and acrylamide, partially hydrolyzed, crosslinked, polyacrylamides such as are defined in US. Pat. 3,247,171, ion exchange resins such as a condensation product of epichlorohydrin and ammonia, polyalkylene oxides, copolymers of alkylene oxides with other organic electrolytes, and the like. In order to possess the necessary properties for use in the process of this invention, the organic polyelectrolytes must have a molecular Weight of at least 30,000 and preferably of at least 50,000. Such polyelectrolytes may be employed either in aqueous solution, spray or mist form or in the form of a finely-divided particulate solid. In general, the most effective size of the particles of polyelectrolyte or polyelectrolyte solution is from about 10 microns to about 50 mesh (Standard sieve size). Particles smaller than 10 microns lose effectiveness in producing coalescence of the atmospheric particles and particles larger than 50 mesh, while effective, begin to significantly reduce the number of particles produced from a given volume of polyelectrolyte and therefore become ineificient.
Since the coagulation and precipitation of the water particles herein is electrostatically produced, it is necessary that at least a portion of the polyelectrolyte employed contains a different charge from that of the fog or cloud to be treated. Therefore, since clouds and fogs usually have an electronegative charge, it is often desirable to employ a cationic electrolyte, or where the fog, cloud, or other particulate mass to be coagulated and dispersed contains a positive charge, an anionic polyelectrolyte may be employed. However, aggregation and precipitation of particles is also accomplished by the addition of a polyelectrolyte of similar charge but of different magnitude and which, therefore, disrupts the electrostatic equilibrium.
The amount of polyelectrolyte or polyelectrolyte solution required for a given atmospheric condition will vary depending upon the density of the atmospheric particles, e.g., the density of the cloud or fog, the depth of the mass of atmospheric particles through which it is to pass, and the like. As each polyelectrolyte particle passes through the mass of atmospheric particles, differently charged particles combine to form a particle of altered electrical charge which falls through the atmospheric mass, collides with other particles to produce a large particle and continues to increase in acceleration and speed until the surface tension is overcome and the particle redivides. Each of the divided particles then continues to fall and grow to produce a chain-reaction of acceleration and division of particles.
Any suitable means may be employer to distribute the polyelectrolyte within the fog, smoke, cloud, or other particle-containing atmospheric mass and thereby produce contact between the dissimilar particles, i.e., the atmospheric particles and the polyelectrolyte particles. For example, spraying a solution of the polyelectrolyte above or within the fog or cloud from an airplane or helicopter, explosively dissiminating the polyelectrolyte within the cloud by means of a bomb or exploding rocket, spraying or blowing the polyelectrolyte from ground vehicles, and the like, produces sufiicient dispersion to cause coalescence and precipitation of the particles and thereby produce dissipation of fog or smoke and rain, snow or other precipitation from clouds.
The following examples are provided to more fully illustrate the invention but are not to be construed as limiting to the scope thereof.
EXAMPLE 1 Steam was injected into a room 20 ft. x 12 ft. x 8 ft. until a dense fog was produced. The degree of fog density was measured by shining a light a distance of 16 feet through the fog and into a light intensity meter such that higher readings are produced on the light intensity with less dense fog and lower readings with more dense fog. A reading of 120 units is achieved when no fog is present.
When the light intensity meter reading stabilized at 18 units, a 10 weight percent aqueous solution of polyethylenimine (having a molecular weight of about 100,000) was sprayed as a fine mist about 4 feet above the beam of light for 10 seconds at the rate of 1 gm. of spray per second. The spray was produced from a Quick-Fill spray bomb powered by C cartridges which was moved back and forth between the light source and the light meter. Within 30 seconds after spraying was started, the light intensity meter showed a reading of 21 units and continued to show a reading of 21 units for a total of two minutes. After a total of five minutes, the fog had returned to the equilibrium value of 18 units. It should be noted that the substantial reduction in fog is produced with an effective particle fall distance of only four feet.
In a control run, a spray of water was employed in place of the spray of polyethylenimine solution. During the ten second period of spraying, the light intensity meter reading decreased to 16 units and remained at this level for about 45 seconds. After a total time of about five minutes from the beginning of the water spraying, the light intensity meter reading returned to the equilibrium value of 18 units.
EXAMPLE 2 In the same manner as Example 1, a weight percent solution of polyethylenpolyamine (Purifloc C-31) having a molecular weight of about 100,000 was sprayed four feet above the beam of light for a period of five seconds at a rate of one gram of spray per second. After 30 seconds from the beginning of application of the spray, the light intensity meter reading had increased to 20 units and remained at this value for a period of one minute. After a total of three minutes, the intensity meter reading had returned to the equilibrium value of 18 units.
EXAMPLE 3 In the manner of Example 1, a weight percent aqueous solution of polyethylenimine having a molecular weight of about 100,000 was sprayed for two minutes along a line four feet above the light beam. During this period the light intensity meter reading rose to a value of 24 units and an additional three minutes was required for the reading to return to the equilibrium value of 18.
When a five weight percent solution of polyethylenepolyamine having a molecular weight of about 100,000 was employed in the same manner, the light intensity meter reading increased to a value of 22 units and an additional two and one-half minutes was required for the reading to return to an equilibrium value of 18 units.
Similar results are obtained when a fine (about 200 mesh) powdered form of a water-swellable, partially hydrolyzed acrylamide polymer containing about 30% by weight sodium acrylate groups and crosslinked with about 1500 ppm. of methylene bisacrylamide is dispersed into the steam in the place of the polyethylenimine or polyalkylenepolyamine.
Likewise, similar results are obtained when a finely divided form of sodium polystyrene sulfonate is employed in the place of the polyethylenimine employed above.
In a control experiment employing water in the place of an aqueous solution of polyethylenimine of polyalkylenepolyamine, the light intensity meter reading decreased to 15 units during the spraying step then increased slowly to the equilibrium value of 18 units in about three minutes.
EXAMPLE 4 In order to demonstrate the applicability of the process of this invention to disperse a warm fog from airport runways under actual field conditions, an experiment was conducted at a large airport in the southern United States. For purposes of the test both a transmissometer and ground observers were employed to determine the effect of the test on visibility. The test was begun at 7:05 am. with an initial visibility of feet to feet with no runway lights visible to the observers. An aircraft was flown over one runway at an altitude of about 500 feet and a 5% solution of polyethylenimine having a molecular weight of about 100,000 was applied at the rate of 200 lbs./ sq. mile in seven passes over the runway. Both transmissometer readings and ground visual observers recorded that visibility rapidly increased with each pass of the spraying operation and by 8:00 am. after six of the seven passes had been completed, visibility had increase to 3200 feet.
EXAMPLE 5 A heavily forested area covered by a large cloud of ascending white-grey smoke from burning saw mill waste was treated with a 5 weight percent aqueous solution of polyethylenimine by spraying a mist of such solution from an airplane just above the smoke (an altitude of about 100 feet). As the polyelectrolyte solution passed into the smoke a definite color change to blue was observed, showing densification of the smake and the color change and densification could be seen continuing down through the rising smoke. After a second application of polyelectrolyte, the forest could be seen through the treated portion of the smoke but was not visibile through the untreated portions.
In a like manner, spraying from aircraft into moistureladen cloud columns of several thousand feet in height with aqueous solutions containing 1 to 10 weight percent polyethylenimine and using a deployment rate of from about 5.0 to 20.0 lbs. of solution per square mile near the top of the clouds results in precipitation of a substantial portion of such clouds in the form of rain. Similar results are achieved when other polyalkylenimines, polyalkylenepolyamines, copolymers of sodium acrylate and acrylamide are employed in place of the polyethylenlmme.
Various modifications can be made in the present invention without departing from the spirit or scope thereof for it is understood that I limit my self only as defined in the appended claims.
I claim:
1. A process for the control of particles suspended in the atmosphere which comprises contacting a mass of suspended atmospheric particles with an organic polyelectrolyte having a molecular weight of at least 30,000 in fine particulate form to modify the electrical charge of said atmospheric particles thereby to produce coalescence and precipitation of such particles.
2. The process according to claim 1 wherein the size of the polyelectrolyte particles is between about 10 microns and about 50 mesh.
3. The process according to claim 1 wherein the molecular weight of the polyelectrolyte is at least 50,000.
4. The process according to claim 1 wherein the polyelectrolyte is a polyalkylenimine.
5. The process according to claim 1 wherein the polyelectrolyte is a polyalkylenimine.
6 References Cited UNITED STATES PATENTS 2,835,530 5/1958 Schneider 239-2 5 2,962,450 11/1960 Elod et a1. 239-14 X ROBERT B. REEVES, Primary Examiner U.S. Cl. X.R.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US68455067A | 1967-11-20 | 1967-11-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3534906A true US3534906A (en) | 1970-10-20 |
Family
ID=24748517
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US684550A Expired - Lifetime US3534906A (en) | 1967-11-20 | 1967-11-20 | Control of atmospheric particles |
Country Status (6)
Country | Link |
---|---|
US (1) | US3534906A (en) |
BE (1) | BE724100A (en) |
DE (1) | DE1805888A1 (en) |
FR (1) | FR1601767A (en) |
GB (1) | GB1214720A (en) |
NL (1) | NL6815376A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3802624A (en) * | 1971-12-21 | 1974-04-09 | Hoechst Ag | Method of and agents for influencing weather |
US3804328A (en) * | 1972-10-13 | 1974-04-16 | Dow Chemical Co | Fog abatement |
US5441200A (en) * | 1993-08-20 | 1995-08-15 | Rovella, Ii; Ernest J. | Tropical cyclone disruption |
US20040134997A1 (en) * | 2001-12-25 | 2004-07-15 | Alexander Khain | Method and apparatus for controlling atmospheric conditions |
US20080035750A1 (en) * | 2006-05-16 | 2008-02-14 | Aylor Robert B | Reduction of cyclonic wind damage |
US20100001118A1 (en) * | 2008-07-03 | 2010-01-07 | Nelson Riley H | Tornado disarming network |
US20100276533A1 (en) * | 2005-12-31 | 2010-11-04 | Matteo Bonifacio Gravina | Thermal Energy Radiance Expander |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3247607A1 (en) * | 1982-12-23 | 1984-07-05 | Zbigniew Dr. 6078 Neu-Isenburg Boguslawski | METHOD FOR REMOVING FOG FROM THE ATMOSPHERA |
DE3344809A1 (en) * | 1983-12-12 | 1985-06-13 | Zbigniew Dr. 6078 Neu-Isenburg Boguslawski | METHOD AND DEVICE FOR REMOVING FOG FROM THE ATMOSPHERA |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2835530A (en) * | 1955-05-13 | 1958-05-20 | Schneider Karl | Process for the condensation of atmospheric humidity and dissolution of fog |
US2962450A (en) * | 1956-04-04 | 1960-11-29 | Elod Egon | Fog dispelling composition |
-
1967
- 1967-11-20 US US684550A patent/US3534906A/en not_active Expired - Lifetime
-
1968
- 1968-10-28 NL NL6815376A patent/NL6815376A/xx unknown
- 1968-10-29 DE DE19681805888 patent/DE1805888A1/en active Pending
- 1968-11-19 BE BE724100D patent/BE724100A/xx unknown
- 1968-11-19 FR FR1601767D patent/FR1601767A/fr not_active Expired
- 1968-11-20 GB GB55179/68A patent/GB1214720A/en not_active Expired
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2835530A (en) * | 1955-05-13 | 1958-05-20 | Schneider Karl | Process for the condensation of atmospheric humidity and dissolution of fog |
US2962450A (en) * | 1956-04-04 | 1960-11-29 | Elod Egon | Fog dispelling composition |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3802624A (en) * | 1971-12-21 | 1974-04-09 | Hoechst Ag | Method of and agents for influencing weather |
US3804328A (en) * | 1972-10-13 | 1974-04-16 | Dow Chemical Co | Fog abatement |
US5441200A (en) * | 1993-08-20 | 1995-08-15 | Rovella, Ii; Ernest J. | Tropical cyclone disruption |
US20040134997A1 (en) * | 2001-12-25 | 2004-07-15 | Alexander Khain | Method and apparatus for controlling atmospheric conditions |
US20100276533A1 (en) * | 2005-12-31 | 2010-11-04 | Matteo Bonifacio Gravina | Thermal Energy Radiance Expander |
US20080035750A1 (en) * | 2006-05-16 | 2008-02-14 | Aylor Robert B | Reduction of cyclonic wind damage |
US20100001118A1 (en) * | 2008-07-03 | 2010-01-07 | Nelson Riley H | Tornado disarming network |
US8153943B2 (en) * | 2008-07-03 | 2012-04-10 | Nelson Riley H | Tornado detection network |
Also Published As
Publication number | Publication date |
---|---|
GB1214720A (en) | 1970-12-02 |
NL6815376A (en) | 1969-05-22 |
DE1805888A1 (en) | 1969-06-26 |
FR1601767A (en) | 1970-09-14 |
BE724100A (en) | 1969-05-19 |
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