US2349300A - Explosive - Google Patents
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- US2349300A US2349300A US425417A US42541742A US2349300A US 2349300 A US2349300 A US 2349300A US 425417 A US425417 A US 425417A US 42541742 A US42541742 A US 42541742A US 2349300 A US2349300 A US 2349300A
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- drying
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- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B21/00—Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
- C06B21/0091—Elimination of undesirable or temporary components of an intermediate or finished product, e.g. making porous or low density products, purifying, stabilising, drying; Deactivating; Reclaiming
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
- B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
- B29C35/08—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
- B29C35/0805—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation
- B29C2035/0822—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation using IR radiation
Definitions
- the final drying operation which has generally been used and considered most satisfactory, involved storing the grains on trays in drying chambers, through which warm air at a temperature up to 55 C. was circulated, for periods varied from several days to 90 days or more, demnding upon the size of the grains and the desired residual content of moisture and other volatile matter.
- this operation has been preceded by an extended water-dry treatment, carried out by storing the powder in suitable vessels and circulating warm water heated to a temperature up to 55 C. therethrough for at least several days.
- This has generally followed a previous solvent-recovery step, in which the powder, while contained in a suitable bin or vessel, was treated with Warm air from which the solvent was subsequently condensed by cooling and recovered for re-use.
- a further object of this invention is the provision of a method whereby the drying of eraplosives is facilitated and expedited.
- Another object of this invention is to provide a process for drying explosives whereby increased safety andeconomy oi operation may be secured red radiation.
- a further object of the invention is the provision of a process for drying explosives whereby a high rate of production may be secured while only a limited amount of explosive is maintained under treatment in any one unit at any given time.
- the foregoing objects may be accomplished by subjecting the explosive material to be dried to the action of controlled near infra- When granular explosives containing volatile matter are passed in thin layers through a bath of such radiation, properly controlled, the volatile matter may be rapidly and efficiently removed without adversely affecting the stability or other'chemical or physical properties of the explosive.
- near infra-red radiation refers to radiation characterized by a wave-length between about 6,000 and 20,000 Angstrom units, such as is obtainable by the use of commercially available infra-red ray carbon or tungsten-filament electric bulbs. Such lamps are characterized by emitting radiation largely within the above stated limits of wave-length.
- the most useful portion of the radiation will generally be that characterized by wave-lengths between 8,000 and 20,000 Angstrom units.
- the explosive material to be dried be supplied in relatively thin layers and that relative motion be provided between the explosive and the source of radiation.
- the explosive mateiial is caused to pass through a bath of radiation by depositing a thin layer on a moving endless belt, which passes through one or more irradiated zones; whereby, deleterious effects due to the incomplete uniforrnity of distribution of the radiation are avoided-and uniform drying results and safety of operation are secured.
- the intensity of radiation, the dimensions of the radiation zone, and the distance from the radiators to the surface of the moving layer are coordinated to achieve a temperature (at the top surface of the layer) which will accomplish the desired drying.
- a temperature in the case of smokeless powder may be to C., as high as C. in the case of dinitromethylaniline, or as high as C. for tetryl; it being understood that it is desirable to employ the highest temperature which is consistent with reasonable stability and safety considerations for the particular explosive being treated.
- the depth of the layer being irradiated depends upon the character of the explosive, the moisture content and the temperature of treatment. In the case of smokeless powder, it is desirable to treat in layers having a thickness oi about /2 inch or less, with dinitromethylaniline about y inch and tetryi about inch.
- globular smokeless powder grains of the type disclosed in United States Patent 2,027,114 may be dried in accordance with this invention by treatment of a continuously moving thin layer with near infrared radiation, utilizing the apparatus shown somewhat. diagrammatically in the accompanying drawing, in which:
- Figure 1 is a plan view of a drying apparatus provided with near infrared radiators according to the present invention.
- Figure 2 is a view in side elevation, with the near side removed, of the apparatus shown in Figure 1.
- Figure 3 is a single linecro'ss-sectional view of the drying apparatusshown in Figure 2.
- Figure 4 is a detail view in cross-section, showing one of the radiators and its arrangement relative to the housingof the drying apparatus.
- the radiators l are preferably arranged as a plurality of zones, whereby the control of temperature is facilitated, each zone of radiators being separately controllable independently of the other zones.
- the radiators may consist of 250 watt, 115 volt infrared bulbs provided with tungsten, carbon, or other suitable filament, each being furnished with areflector of suitable shape and surface characteristics, such as of plated,
- the radiators are so adjusted in the reflectors ii that the radiation on the belt, 18 inches below the mouths of the reflectors, is diffuse,
- the reflector mouths are covered by a layer of material it, such as a mica sheet, which is transparent to the desired radiation, to prevent any possible access of explosive dust or gas mixture to the heated surface of the lam is or, in case of breakage,
- An installation comprising 140 lamps arranged in three distinct control zones has been found efiective, the lamps being more densely grouped in the zone between the hopper i and line 8 than in the zones between lines 8 and 9 and to the right of line 9.
- the endless. belt 2 may be of any suitable material and is preferably provided having a surface which reflects the impinging radiation so as to minimize the chances for an undue rise in temperature.
- Continuous travel of the belt at the desired slow rate may be accomplished by rotating the discharge-end pulley by means of an electric motor, through reduction gears and an adjustable drive of known typ
- the temperature of the material on the belt 2 within the drying chamber 3 may be controlled at the desired value by means of thermocouples and associated control apparatus.
- to 29, inclusive may be distributed in the chamberso as to contact the uppermost surface of the layer of powder grains.
- the central couple in each zone may be connected with a recording and controlling potentiometer, by means of which temperature readings may be taken at frequent intervals and. whenever necessary, a relay, turning the lamps in any one zone on or off, may be operated.
- Dinitromethylaniline may be dried in the abovedescribed apparatus from'a moisture content of about 5% to about 0.1% by subjecting the material in a layer inch thick to irradiation by the infrared lamps for a period of 5 minutes, the operation of the lamps being controlled to maintain a temperature of 95 C.- in the air space just above the product being treated. Under these conditions, each unit is capable of yielding at least 150 pounds of dried product per hour. Dther operating conditions may be employed to attain this or higher production capacity; for example, the use of thicker layers, higher temperatures, and different rates of belt travel may so be coordinated as to attain such results.
- this material having a V moisture content of 30% may be fed into the above-described apparatus as a uniform layer,
- tetryl having a, moisture content of 7 to 12%
- tetryl having a, moisture content of 7 to 12%
- tetryl having a, moisture content of 7 to 12%
- tetryl having a, moisture content of 7 to 12%
- a single unit of the character hereinbefore described is capable of drying 1,200 pounds of tetryl to a moisture content of 0.03 to 0.05% in the twenty-four hour period.
- 2,100 pounds of tetryl can be dried intwenty-four hoursto a final moisture content or 0.1%.
- globular grains of about 0.035 inch diameter may be dried from a. content of 9.8% olatile matter to not more than 1.2% at a production rate of over 50 pounds per hour, the drying temperature being controllcdat about 75 C. and the optimum layer thickness in this case being about inch.
- the optimum conditions for the drying of any given granular explosive material may vary with the grain size and density but can readily be established by determining the capacity of the apparatus at various layer thicknesses at the desired operating temperature, the speed of travel or the conveying belt being adjusted to accomplish the required extent of drying.
- nitro explosive is used in the appended claims in a sense which is inclusive of the several organic explosive materials herein specifically referred to, to-wit, smokeless powder (nitrocellulose), tetryl, trinitrotoluene, trinitroresorcin, picric acid, ammonium picrate and dinitromethyianiline.
- the process of drying wet granular organic nitro explosive material comprising, feeding the wet material upon a conveyor, moving the laden conveyor through an enclosure irradiated with near infra .red light of an intensity such as to maintain a temperature of at least 65 C. at the upper surface of the grains on the conveyor, moving the con veyor at a rate such that the grains remain in radiation zone for at least five minutes, and dis charging the material from the conveyor at the end of the enclosure.
- the process of drying wet smokeless powder grains comprising, feeding the wet grains upon a conveyor, moving the conveyor through an enclosure irradiated with near infrared light of an intensity such as to maintain a temperature of 65-75" (C. at the upper surface of the grains on the conveyor, and moving the conveyor at a rate such that the powder grains remain in the irradiation zone from one to two hours.
- the process of drying wet granular dinitromethylaniline comprising, feeding the wet grains upon a con veyor, moving the conveyor through an enclosure irradiated with near infrared light of an intensity such as to maintain a temperature of approxi- 25 mately 95 C. at the upper surface of the grains 'on the conveyor, and moving the conveyor at a rate such that the grains remain in the irradiation zone for at least five minutes.
- the process 30 of drying wet granular tetryl comprising, feeding the wet grains upon a conveyor, moving the conveyor through an enclosure irradiated with near infrared light of an intensity such as to maintain a temperature of approximately 110 C. at the upper surface of the grains on the conveyor, and moving the conveyor at a rate such that the grains remain in the irradiation zone from two to four hours.
Description
F. OLSEN May 23, 1944.
EXPLOS IVE 3 m Q & & 2w \9 D m m w m b .m i M ccccjkkcc C C C CCFAQLFWHCCCCCCCXC m m x Q x x o A G 0 o 0 0 0 0 0 0 0 @000090000000000 Q 0 0 0 0 0 0 o 0 Q Q 0 0000000090000000 o 09 0 0 0 000 0 Q 0 6090000900060090 0090 o 0900 00 0 0009000000009000 Q 0 0 0 pm 0 90.0 0 o QQQQQOQQQOQQ UO M w Patented May 23, 1944 UNITED STATES PATENT OFFICE EXPLOSIVE Fredric]: Olsen, Alton, lll., assignor to Weatem Cartridge Company, East Alton, Ill., a corporation or Delaware Application January 2, 1942, Serial No. 425,417
4 Claims. (Cl. 34-39) The step of drying has been an essential part of the manufacture of explosives required to have a minimum content of moisture and/or other volatile matter, such as organic solvents. Heretofore, the methods which have been available for the removal of volatile matter from explosives have been fraught with disadvantageous features, particularly the exceedingly long drying period required and the necessity for spacing the buildings in which the drying is accomplished inconveniently large distances apart, which not only results in the waste of a considerable proportion of the plant area but also requires the erection and maintenance of extended steam, air and power lines.
Thus, in the manufacture of smokeless powder grains, the final drying operation, which has generally been used and considered most satisfactory, involved storing the grains on trays in drying chambers, through which warm air at a temperature up to 55 C. was circulated, for periods varied from several days to 90 days or more, demnding upon the size of the grains and the desired residual content of moisture and other volatile matter. Frequently, this operation has been preceded by an extended water-dry treatment, carried out by storing the powder in suitable vessels and circulating warm water heated to a temperature up to 55 C. therethrough for at least several days. This has generally followed a previous solvent-recovery step, in which the powder, while contained in a suitable bin or vessel, was treated with Warm air from which the solvent was subsequently condensed by cooling and recovered for re-use.
Likewise, extended drying periods have heretofore been required in'the manufacture of explosives such as the aromatic nitro compounds, for example trinitrophenylmethylnitramin (tetryl), trinitrotoluene, trinitroresorcin, picric acid,'and ammonium picrate. As an illustration, in order to reduce the moisture content of tetryl from 25% to the desired residue of less than 0.1%, it has been necessaryto store the explosive in trays within a drier chamber through which air heated to a temperature of 70 C. was circulated for a minimum period of 45 hours.
One unavoidable consequence of this prior method of drying was the necessity for storing large weights of explosive undergoing th drying treatment in the individual dry-houses. For
reasons of safety. it has been considered essential to segregate each of such buildings in order to minimize the chances of having an accidental explosion in one of the drier chambers spread throughout the entire drying installation of the plant. The minimum distance of separation between buildings depends upon the character and amount of the explosive under treatment and may be computed by the use of formulas or taken from tables compiled as a result of previous experience. It will readily be apparent, however, that for a plant of given capacity of explosives, the plan of having only a small quantity of explosives stored in any one buildl would have the disadvantage of requiring a very large number of smalidryhouses, while, if the capacity of the individual dryhouses is increased, this is necessarily accompanied by an increase in the area segregated for this purpose, since larger distances must then he provided between the units.
In view of the serious disadvantages which dried or partly dried state, are exceedingly poor conductors of heat and also, very unfavorable conditions of heat transfer are encountered when attempts are madeto supply heat to such a mass by means of a heated plate or belt or by means of a heated gaseous medium. Furthermore, when the explosive produced is in the form of very small particles, as isv generally the case with the aromatic nitro explosives, gaseous drying media cannot be employed at high velocity. since otherwise, particles of the material under treatment become entrained with the gas.
It is an object of this invention to provide a. method for drying explosives which overcomes the disadvantages of prior methods.
A further object of this invention is the provision of a method whereby the drying of eraplosives is facilitated and expedited.
Another object of this invention is to provide a process for drying explosives whereby increased safety andeconomy oi operation may be secured red radiation.
It is also an object of this invention to provide a process for drying explosives which enables the operation to he carried out continuously.
A further object of the invention is the provision of a process for drying explosives whereby a high rate of production may be secured while only a limited amount of explosive is maintained under treatment in any one unit at any given time.
Other objects will appear from the following detailed description.
In accordance with this invention, generally stated, the foregoing objects may be accomplished by subjecting the explosive material to be dried to the action of controlled near infra- When granular explosives containing volatile matter are passed in thin layers through a bath of such radiation, properly controlled, the volatile matter may be rapidly and efficiently removed without adversely affecting the stability or other'chemical or physical properties of the explosive.
The term near infra-red radiation" refers to radiation characterized by a wave-length between about 6,000 and 20,000 Angstrom units, such as is obtainable by the use of commercially available infra-red ray carbon or tungsten-filament electric bulbs. Such lamps are characterized by emitting radiation largely within the above stated limits of wave-length. For the purpose of the present invention, the most useful portion of the radiation .will generally be that characterized by wave-lengths between 8,000 and 20,000 Angstrom units.
it has been found that explosive substances which are characterized by the presence of nitro or nitrate groups are to a large extent transparent in very thin layers to radiation of the above-described character, whereas practically complete absorption and conversion to heat result when water and the common organic solvents'are subjected to radiation of wave-lengths greater than 8,000 Angstrom units. Advantage is taken of this behavior, in the process of this invention, in facilitating the transfer of energy from top to bottom of the layer of granular explos'ive under treatment, as well as to the interiorsof the individual particles or grains of the explosive. This factor contributes largely toward enabling the drying operation (with near infrared radiation) to be carried out rapidly, so that temperatures may be employed which could not be tolerated with other types of heat transfer. For example, in the case of smokeless powder drying, it is entirely satisfactory'and, indeed, advantageous, to subject the powder (under near infrared radiation) to temperatures in excess of the temperature (65 C.) usually employed in surveillance tests.
' The radiant energy is apparently most readily absorbed and converted to heat in regions of the explosive which contain volatile matter and is accordingly most effective where it is most needed. Likewise, since the energy is transferred in the form of penetrating radiation, the serious obstacle of poor heat transfer, which greatly decreases the efilciency of drying processes in which reliance is had on heating by means of a heated gas or metal belt or tray, is not encountered in the process ofthis invention. In contrast to the prior drying methods, in which the transfer of heat to the interior of the mass of explosive material becomes increasingly more diificult as the drying progresses, the present process offers the unique advantage of providing conditions wherein the penetration of energy may be facilitated to an increasing extent as the drying proceeds. This is of particular signiflcance in view of the recognized fact that the removal (by the means hitherto employed) of the last percent or so of volatile matter from explosives, generally proves to be the most difflcult.
In accordance with the present process, it has been found essential that the explosive material to be dried be supplied in relatively thin layers and that relative motion be provided between the explosive and the source of radiation. Preferably, the explosive mateiial is caused to pass through a bath of radiation by depositing a thin layer on a moving endless belt, which passes through one or more irradiated zones; whereby, deleterious effects due to the incomplete uniforrnity of distribution of the radiation are avoided-and uniform drying results and safety of operation are secured.
The intensity of radiation, the dimensions of the radiation zone, and the distance from the radiators to the surface of the moving layer are coordinated to achieve a temperature (at the top surface of the layer) which will accomplish the desired drying. Such a temperature, in the case of smokeless powder may be to C., as high as C. in the case of dinitromethylaniline, or as high as C. for tetryl; it being understood that it is desirable to employ the highest temperature which is consistent with reasonable stability and safety considerations for the particular explosive being treated.
The depth of the layer being irradiated depends upon the character of the explosive, the moisture content and the temperature of treatment. In the case of smokeless powder, it is desirable to treat in layers having a thickness oi about /2 inch or less, with dinitromethylaniline about y inch and tetryi about inch. The speed at which the layer is moved through the irradiation zone also depends upon other factors, such as the moisture content, the temperature and the thickness of the layer, but particularly upon the length of the irradiation zone, as the controlling element is the elapsed time of irra-= diation rather than speed of travel. This may be 1-2 hours for smokeless powder, 3-4 hours for tetryl, or as little as 5 minutes for dinitromethylaniline.
Another factor which must be considered in determining the temperatures, layer depth and irradiation time of any given explosive is the character of the conveyor member, particularly its heat conductivity and light'reiiecting characteristics. For example, a white rubber conveyor belt contributes definitely toward the achievement of uniformity of heating. Furthermore, while the invention is disclosed herein with particular reference to layers of material in which the relation of the grains in the layer is substantially constant throughout the treatment, it is evident that suitable agitators or conductor blades may be provided for turning or causing exercised not to utilize devices which will induce such intra-layer migration when the explosive is of a character in which friction due to movement of one grain over another may cause detonation.
As an illustrative example, globular smokeless powder grains of the type disclosed in United States Patent 2,027,114 may be dried in accordance with this invention by treatment of a continuously moving thin layer with near infrared radiation, utilizing the apparatus shown somewhat. diagrammatically in the accompanying drawing, in which:
Figure 1 is a plan view of a drying apparatus provided with near infrared radiators according to the present invention.
Figure 2 is a view in side elevation, with the near side removed, of the apparatus shown in Figure 1.
Figure 3 is a single linecro'ss-sectional view of the drying apparatusshown in Figure 2.
Figure 4 is a detail view in cross-section, showing one of the radiators and its arrangement relative to the housingof the drying apparatus.
Powder grains containing about 12% volatile matter, consisting of moisture and residual orof the drying chamber a plurality of radiators i are arranged in banks.
The radiators l are preferably arranged as a plurality of zones, whereby the control of temperature is facilitated, each zone of radiators being separately controllable independently of the other zones. The radiators may consist of 250 watt, 115 volt infrared bulbs provided with tungsten, carbon, or other suitable filament, each being furnished with areflector of suitable shape and surface characteristics, such as of plated,
gold or aluminum. Preferably, the radiators are so adjusted in the reflectors ii that the radiation on the belt, 18 inches below the mouths of the reflectors, is diffuse, The reflector mouths are covered by a layer of material it, such as a mica sheet, which is transparent to the desired radiation, to prevent any possible access of explosive dust or gas mixture to the heated surface of the lam is or, in case of breakage,
of heated fragments of glass or filament to the layer of explosive material. An installation comprising 140 lamps arranged in three distinct control zones has been found efiective, the lamps being more densely grouped in the zone between the hopper i and line 8 than in the zones between lines 8 and 9 and to the right of line 9.
The endless. belt 2 may be of any suitable material and is preferably provided having a surface which reflects the impinging radiation so as to minimize the chances for an undue rise in temperature. A whit rubber composition belt, 1%- inch thick, 4 ft. wide, and travelling over pulleys 39 feet apart between centers, has been found satisfactory. Continuous travel of the belt at the desired slow rate may be accomplished by rotating the discharge-end pulley by means of an electric motor, through reduction gears and an adjustable drive of known typ The temperature of the material on the belt 2 within the drying chamber 3 may be controlled at the desired value by means of thermocouples and associated control apparatus. Thus, nine thermocouples, 2| to 29, inclusive, may be distributed in the chamberso as to contact the uppermost surface of the layer of powder grains. The central couple in each zone may be connected with a recording and controlling potentiometer, by means of which temperature readings may be taken at frequent intervals and. whenever necessary, a relay, turning the lamps in any one zone on or off, may be operated.
'The remaining six couples are connected to selector switches and thereby to an indicating potentiometer, permitting the measurement of the temperature, whenever desired, at any of the six points. Switches may also be provided for controlling the successive rows of lamps.
It may be desirable to provide a gentle circulation of air or other gas over the grains in order to remove the vaporized volatile matter. This may be accomplished by passing a slow current of warm air into drying chamber 3 by means of a duct i0 located at the discharge end, through the chamber 3, and out through a hood I! located at the charging end and provided with a stack l2. The vapor discharged through stack i2 may b subjected to solvent recovery treatment if that should be desired.
Excellent results have been obtained by adjusting the depth of the powder grain layer at close to inch, and the speed of travel of the belt such that 95 minutes are required for passing through the radiation chamber (approximately 30 feet), the temperature being maintained at close to 72 C. Under these operating conditions, a unit of this type reducesthe moisture and volatile content of globular smokeless powder grains, of about 0.020 inch diameter and 0.950 gravimetric density, from 12% to not more than 0.9% at the rate of 60 pounds per hour. When the initial content of volatile matter amounts to "810%, the capacity -of each unit as described above is increasedto at least 80-85 pounds per hourof smokeless powder containing about 1.1 to 1.2% residual volatile matter.
Dinitromethylaniline may be dried in the abovedescribed apparatus from'a moisture content of about 5% to about 0.1% by subjecting the material in a layer inch thick to irradiation by the infrared lamps for a period of 5 minutes, the operation of the lamps being controlled to maintain a temperature of 95 C.- in the air space just above the product being treated. Under these conditions, each unit is capable of yielding at least 150 pounds of dried product per hour. Dther operating conditions may be employed to attain this or higher production capacity; for example, the use of thicker layers, higher temperatures, and different rates of belt travel may so be coordinated as to attain such results.
In another embodiment illustrating the drying of dinitromethylaniline, this material having a V moisture content of 30% may be fed into the above-described apparatus as a uniform layer,
- inch in thickness, and passed therethrough in 8 minutes. By maintaining a temperature of C. in the charging zone and 120 C. in the discharging zone, a product having a residual moisture content of 0.4% is obtainable at a production rate of 75 pounds per hour. Y
As another example, tetryl, having a, moisture content of 7 to 12%, may be dried in accordance with the present inventionby depositing it upon the belt in a layer about A inch thick; controlling the temperature at the top surface of the layer to about C. and adjusting thespeed of the belt to a rate that about 3 /2 hour is required for movement through the irradiation zone. Under these conditions, a single unit of the character hereinbefore described is capable of drying 1,200 pounds of tetryl to a moisture content of 0.03 to 0.05% in the twenty-four hour period. Using the same conditions as above indicated. excepting that the irradiation period is reduced to two hours, 2,100 pounds of tetryl can be dried intwenty-four hoursto a final moisture content or 0.1%.
As a further example of the drying of smokeless powder, globular grains of about 0.035 inch diameter may be dried from a. content of 9.8% olatile matter to not more than 1.2% at a production rate of over 50 pounds per hour, the drying temperature being controllcdat about 75 C. and the optimum layer thickness in this case being about inch. v
The optimum conditions for the drying of any given granular explosive material may vary with the grain size and density but can readily be established by determining the capacity of the apparatus at various layer thicknesses at the desired operating temperature, the speed of travel or the conveying belt being adjusted to accomplish the required extent of drying.
The expression nitro explosive" is used in the appended claims in a sense which is inclusive of the several organic explosive materials herein specifically referred to, to-wit, smokeless powder (nitrocellulose), tetryl, trinitrotoluene, trinitroresorcin, picric acid, ammonium picrate and dinitromethyianiline.
Having thus described the invention, what I claim is:
1. In the manufacture of explosives, the process of drying wet granular organic nitro explosive material, comprising, feeding the wet material upon a conveyor, moving the laden conveyor through an enclosure irradiated with near infra .red light of an intensity such as to maintain a temperature of at least 65 C. at the upper surface of the grains on the conveyor, moving the con veyor at a rate such that the grains remain in radiation zone for at least five minutes, and dis charging the material from the conveyor at the end of the enclosure.
2. In the manufacture of explosives, the process of drying wet smokeless powder grains, comprising, feeding the wet grains upon a conveyor, moving the conveyor through an enclosure irradiated with near infrared light of an intensity such as to maintain a temperature of 65-75" (C. at the upper surface of the grains on the conveyor, and moving the conveyor at a rate such that the powder grains remain in the irradiation zone from one to two hours.
3. In the manufacture of explosives, the process of drying wet granular dinitromethylaniline, comprising, feeding the wet grains upon a con veyor, moving the conveyor through an enclosure irradiated with near infrared light of an intensity such as to maintain a temperature of approxi- 25 mately 95 C. at the upper surface of the grains 'on the conveyor, and moving the conveyor at a rate such that the grains remain in the irradiation zone for at least five minutes.
4. In the manufacture of explosives, the process 30 of drying wet granular tetryl, comprising, feeding the wet grains upon a conveyor, moving the conveyor through an enclosure irradiated with near infrared light of an intensity such as to maintain a temperature of approximately 110 C. at the upper surface of the grains on the conveyor, and moving the conveyor at a rate such that the grains remain in the irradiation zone from two to four hours.
iii
FREDRICH OLSEN.
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Cited By (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2428090A (en) * | 1944-05-17 | 1947-09-30 | Gump B F Co | Infrared treatment of cereal germs |
US2438227A (en) * | 1944-07-10 | 1948-03-23 | Jonas & Naumburg Corp | Apparatus for treating fur-bearing animal skins |
US2438226A (en) * | 1944-07-10 | 1948-03-23 | Jonas & Naumburg Corp | Carroting and drying of fur-bearing animal skins |
US2446822A (en) * | 1943-08-11 | 1948-08-10 | Herbert L Grapp | Method and apparatus for removing volatiles from articles involving the use of infra-red lamps |
US2450590A (en) * | 1946-02-18 | 1948-10-05 | Frank C Gullo | Fruit drier |
US2459915A (en) * | 1945-06-25 | 1949-01-25 | Harry M Sherman | Conveyer for dehydrating machines |
US2474952A (en) * | 1944-09-30 | 1949-07-05 | William J Miskella | Apparatus for heating and drying granular material in a continuously flowing stream |
US2527062A (en) * | 1946-08-05 | 1950-10-24 | Colgate Palmolive Peet Co | Method of conditioning bar soap for pressing by means of infrared radiation |
US2529704A (en) * | 1944-02-24 | 1950-11-14 | Olin Ind Inc | Method of drying ammunition primers |
US2575426A (en) * | 1947-12-22 | 1951-11-20 | American Machinery Corp | Method of and apparatus for treating edible produce |
US2577209A (en) * | 1948-06-10 | 1951-12-04 | Bernard J Hoffman Jr | Infrared release of water of crystallization |
US2705137A (en) * | 1949-12-16 | 1955-03-29 | Bayer Ag | Belt drier heated by radiation |
US2728387A (en) * | 1953-05-01 | 1955-12-27 | Jr Horace L Smith | Apparatus for drying culture media and analogous materials |
US2745940A (en) * | 1953-05-25 | 1956-05-15 | William R Stroh | Temperature control for brooder |
US2826166A (en) * | 1955-05-06 | 1958-03-11 | Research Corp | Automatic controlled electrostatic coating apparatus |
US2846319A (en) * | 1955-07-26 | 1958-08-05 | E J Kelly & Associates Inc | Drying process |
US2848821A (en) * | 1953-08-26 | 1958-08-26 | Albert R Clark | Drying apparatus |
US2874482A (en) * | 1953-08-17 | 1959-02-24 | Bayer Ag | Drying of moist material |
US2896058A (en) * | 1959-07-21 | perryman | ||
US2924272A (en) * | 1955-05-06 | 1960-02-09 | Chain Belt Co | Method of and apparatus for dehydrating material |
US2935594A (en) * | 1958-08-26 | 1960-05-03 | christenson | |
US3066211A (en) * | 1959-06-04 | 1962-11-27 | Vogt Edmund | Method and apparatus for heating thermoplastic sheets |
US3087041A (en) * | 1957-10-09 | 1963-04-23 | Era Heater Corp | Space heater |
US3116399A (en) * | 1961-01-17 | 1963-12-31 | Wiegand Co Edwin L | Radiant heating apparatus |
US3119355A (en) * | 1959-10-23 | 1964-01-28 | Verband Deutscher Konsumgenoss | Apparatus for the baking of bread and other bakery products with infra-red rays |
US3204341A (en) * | 1961-11-27 | 1965-09-07 | Ashland Oil Inc | Process and apparatus for drying wet particulate material to a desired moisture content |
US3432397A (en) * | 1965-02-23 | 1969-03-11 | Clyde H O Berg | Method of retorting solids |
US3456357A (en) * | 1968-02-05 | 1969-07-22 | Commercial Solvents Corp | Process for continuous automated vibrational drying of explosives and apparatus |
US3591767A (en) * | 1969-06-23 | 1971-07-06 | David Jeffrey Mudie | Radiant shrink tunnel |
US3975618A (en) * | 1974-02-14 | 1976-08-17 | Heidenreich & Harbeck Zweingniederlassung Der Gildemeister Ag | Method and apparatus for heating synthetic plastic components |
US4104804A (en) * | 1974-04-18 | 1978-08-08 | Sargeant Ralph G | Method for drying explosive materials |
US20070234587A1 (en) * | 2006-04-10 | 2007-10-11 | Woodhaven Capital Corp. | Grain drying aeration system |
US20080099459A1 (en) * | 2006-10-05 | 2008-05-01 | Plastech Engineered Products, Inc. | Hybrid infrared convection paint baking oven and method of using the same |
CN106322956A (en) * | 2015-07-01 | 2017-01-11 | 中国五洲工程设计集团有限公司 | Automated grain-airing aging device for propellant high in slenderness ratio |
-
1942
- 1942-01-02 US US425417A patent/US2349300A/en not_active Expired - Lifetime
Cited By (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2896058A (en) * | 1959-07-21 | perryman | ||
US2446822A (en) * | 1943-08-11 | 1948-08-10 | Herbert L Grapp | Method and apparatus for removing volatiles from articles involving the use of infra-red lamps |
US2529704A (en) * | 1944-02-24 | 1950-11-14 | Olin Ind Inc | Method of drying ammunition primers |
US2428090A (en) * | 1944-05-17 | 1947-09-30 | Gump B F Co | Infrared treatment of cereal germs |
US2438227A (en) * | 1944-07-10 | 1948-03-23 | Jonas & Naumburg Corp | Apparatus for treating fur-bearing animal skins |
US2438226A (en) * | 1944-07-10 | 1948-03-23 | Jonas & Naumburg Corp | Carroting and drying of fur-bearing animal skins |
US2474952A (en) * | 1944-09-30 | 1949-07-05 | William J Miskella | Apparatus for heating and drying granular material in a continuously flowing stream |
US2459915A (en) * | 1945-06-25 | 1949-01-25 | Harry M Sherman | Conveyer for dehydrating machines |
US2450590A (en) * | 1946-02-18 | 1948-10-05 | Frank C Gullo | Fruit drier |
US2527062A (en) * | 1946-08-05 | 1950-10-24 | Colgate Palmolive Peet Co | Method of conditioning bar soap for pressing by means of infrared radiation |
US2575426A (en) * | 1947-12-22 | 1951-11-20 | American Machinery Corp | Method of and apparatus for treating edible produce |
US2577209A (en) * | 1948-06-10 | 1951-12-04 | Bernard J Hoffman Jr | Infrared release of water of crystallization |
US2705137A (en) * | 1949-12-16 | 1955-03-29 | Bayer Ag | Belt drier heated by radiation |
US2728387A (en) * | 1953-05-01 | 1955-12-27 | Jr Horace L Smith | Apparatus for drying culture media and analogous materials |
US2745940A (en) * | 1953-05-25 | 1956-05-15 | William R Stroh | Temperature control for brooder |
US2874482A (en) * | 1953-08-17 | 1959-02-24 | Bayer Ag | Drying of moist material |
US2848821A (en) * | 1953-08-26 | 1958-08-26 | Albert R Clark | Drying apparatus |
US2826166A (en) * | 1955-05-06 | 1958-03-11 | Research Corp | Automatic controlled electrostatic coating apparatus |
US2924272A (en) * | 1955-05-06 | 1960-02-09 | Chain Belt Co | Method of and apparatus for dehydrating material |
US2846319A (en) * | 1955-07-26 | 1958-08-05 | E J Kelly & Associates Inc | Drying process |
US3087041A (en) * | 1957-10-09 | 1963-04-23 | Era Heater Corp | Space heater |
US2935594A (en) * | 1958-08-26 | 1960-05-03 | christenson | |
US3066211A (en) * | 1959-06-04 | 1962-11-27 | Vogt Edmund | Method and apparatus for heating thermoplastic sheets |
US3119355A (en) * | 1959-10-23 | 1964-01-28 | Verband Deutscher Konsumgenoss | Apparatus for the baking of bread and other bakery products with infra-red rays |
US3116399A (en) * | 1961-01-17 | 1963-12-31 | Wiegand Co Edwin L | Radiant heating apparatus |
US3204341A (en) * | 1961-11-27 | 1965-09-07 | Ashland Oil Inc | Process and apparatus for drying wet particulate material to a desired moisture content |
US3432397A (en) * | 1965-02-23 | 1969-03-11 | Clyde H O Berg | Method of retorting solids |
US3456357A (en) * | 1968-02-05 | 1969-07-22 | Commercial Solvents Corp | Process for continuous automated vibrational drying of explosives and apparatus |
US3591767A (en) * | 1969-06-23 | 1971-07-06 | David Jeffrey Mudie | Radiant shrink tunnel |
US3975618A (en) * | 1974-02-14 | 1976-08-17 | Heidenreich & Harbeck Zweingniederlassung Der Gildemeister Ag | Method and apparatus for heating synthetic plastic components |
US4104804A (en) * | 1974-04-18 | 1978-08-08 | Sargeant Ralph G | Method for drying explosive materials |
US20070234587A1 (en) * | 2006-04-10 | 2007-10-11 | Woodhaven Capital Corp. | Grain drying aeration system |
US7568297B2 (en) * | 2006-04-10 | 2009-08-04 | Woodhaven Capital Corp. | Grain drying aeration system |
US20080099459A1 (en) * | 2006-10-05 | 2008-05-01 | Plastech Engineered Products, Inc. | Hybrid infrared convection paint baking oven and method of using the same |
US8367978B2 (en) * | 2006-10-05 | 2013-02-05 | Magna International Inc. | Hybrid infrared convection paint baking oven and method of using the same |
CN106322956A (en) * | 2015-07-01 | 2017-01-11 | 中国五洲工程设计集团有限公司 | Automated grain-airing aging device for propellant high in slenderness ratio |
CN106322956B (en) * | 2015-07-01 | 2018-08-21 | 中国五洲工程设计集团有限公司 | A kind of automation of high-fineness ratio propellant is dried in the air medicine ageing device |
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