ARMY MIL-D-46262 A-1965 DETONATOR STAB M20 LOADING ASSEMBLING AND PACKING《M20型针刺雷管的装载 组装和包装》.pdf
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1、MILD46262A (MU) 3 JUNE 1965 SUPERSEDING MIL-D-46262 (ORD) 19 AUGUST 1960 MIZSTARY SFEQFICATION DETONATOR, STAB, M20 LOADING, ASSEMBLING AND PACKING 1. SCOPE 1.1 This specification covers the loading, assembling and packing for one type of stab detonator designated as Detonator, Stab, M20. 2. APPLICA
2、BLE DOCUMENTS 2.1 The following documents of the issue in effect on dae of invitation for bids, or request for proposals, form a part of this specification to the extent specified herein. SPECIFICATIONS MILITARY li5L-P-116 - Preservation, Methods of. MILA-2550 -Ammunition and Spe- cial Weapons, Gen-
3、 eral Specification for. MILI45607 -Inspection Equipment, Supply and Main- tenance of. STANDARDS MILITARY MIMTD-105 - Sampling Procedures and Tables for In- spection by Attrib- utes (ABC-STD- - - - - ._ - 105). : MIL-STD-109 -Quality Assurance Terms and Defini- tions. MIL-STD-650 - Explosive: Sampli
4、ng, Inspection and Test- ing. MIL-STD-1235- Single an d Multilevel Continuous Sampling Procedures and Tables for Inspection by Attributes. DRAWJNGS ORDNANCE CORPS 7548099 - Box, Packing, Ammunition for Detonators. 7548103 - Box, Set-up, Packing Ammu- nition, Outer for Boosters, Detonators, or bers,
5、Assembly, Details, Packing and Marking. 7548104 - Box, Set-up, Packing Ammu- nition, Inner, for Boosters, Detonators and Primers, Assembly, Details, Packing and Marking. 8797752 - Detonator, Stab, M20, Load- ing Assembly. PUBLICATIONS ORDNANCE CORPS IEL-8797752 - Index of Inspection Equipment Lists.
6、 - Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-r MIL-D-46262A 13 I 999790b 0310520 3 I (Copies of speciilcations, standards, drawings and publications required by suppliers in connection with specific procurement functions should be obtained from
7、 the procuring activity or as directed by the contrading officer.) ing agent. Exterior surface coatings shall be continuous except for a few light scratches not exposing base material. AU required markings shall be neat and sharply defined. All packing components shali be dry. 3. REQUIREIWNTS 4. QUA
8、LITY ASSURANCE PROVISIONS 3.1 Material. Materials shall be in accord- ance with applicable drawings and specifi-. cations. 3.2 Detonator. The detonator shall comply with ali- requirements specified on Drawing (dwg.) 8797752 and with all requiremenik specified in applicable specifications. 3.3 Moistu
9、re content of lead azide. The moisture content of the lead azide used in loading the detonator shall not exceed 0.50 percent when tested as specified in 43.1. 3.4 Moisture content of primer mixture. The moisture content of the primer mixture used in loading the detonator shall not ex- ceed 0.30 perc
10、ent when tested as specified in 4.3.3. 3.5 Functioning. 3.5.1 Spmmt. The contractor shall make available to the Government all in- spection and test equipment necessary for de- termining conformance with contract require- ments. Personnel for operating the equipment, and verification of its accuracy
11、, shall be sup- plied by the contractor for the performance of examination or test by the Government. 4.3 Test methods and procedures, 4.3.1 Moisture content of lead azide. The moisture content of the lead azide shall be de- termined in accordance with MIL-STD-650 Method 101.5 except, use a two gram
12、 sample and cover the dish with a sheet of polytetra- fluorothylene. 4.3.2 Detemimtima of binder-lubl-icant con tent of tetryl. An accurately weighed portion of 5 grams shall be transferred to a tared medium porosity sintered glass filtering cruc- ible. The sample shall be extracted with four 10 mil
13、ligram (mi.) portions of acetone main- taining each portion in contact with the resi- due for approximately 5 minutes before apply- ing suction. Any lumps which may persist shall be broken up and the sides of the cruc- ible washed down with each 10 mi. portion of acetone to insure complete removal o
14、f the tetryl. The residue shall be aspirated until the odor of acetone is no longer detectable. The crucible and contents shall be placed in a dry- ing oven at 100 degrees Centigrade (C.), 150 degrees C. for 1/2 hour, cooled in a desicatm and weighed. The above extraction shall be re- peated drying
15、and weighing with individual 10 ml. portions of acetone until the loss in weight on subsequent extractions totals less than 0.005 gram. The weight of residue in the crucible shall be calculated to the percent- age of total binder-lubricant, 43.3 Moisture content of primer mixture. The moisture conte
16、nt of the primer mixture shall be dekrmined in accordance with MIE STD-650 Method 101.5 except, use a one gram sample. 4.3.4 Cmpos;im of prmr mhture. The composition of the primer mixture shall be determined by performing the following tests in the sequence specified : 6 Provided by IHSNot for Resal
17、eNo reproduction or networking permitted without license from IHS-,-,- NIL-D-46262A 13 = 797770b 4.3.4.1 Potassium chkate. Approximately 1 gram of the primer mixture shall be accu- rately weighed and transferred to a tared fil- terhg crucible of approximately 15 ml. capac- ity. Three ml. of lead azi
18、de-saturated distilled water hll be added at a temperature of 25 degrees C. plus or minus 2 degrees C., agitated for exactly 1 minute, and if necessary, any lumps shall be broken up with a glass rod, taking care not to disturb the asbestos mat. Suction shall be applied. This procedure shall be repea
19、ted five times making a total of six 3 ml. extractions. The sample shall be rinsed the filtering crucible with a few ml. of alcohol and ether, dried for approximately 15 minutes at 95 degrees C. plus or minus 2 de- grees C., cooled in a desiccator and weighed. The loss in weight shall be calculated
20、as the percentage of potassium chlorate. 4.3,4.2 Leud mide. The residue remaining from the potassium chlorate determination shall be extracted with 6 mi. portions of satu- rated ammonium acetate solution at about 25 degrees C. (hot saturated ammonium acetate solution must not be used as it dissolves
21、 anti- mony sulfide to some extent) each portion be- ing agitated for about 30 seconds, until the washings no longer give a yellow precipitate mith a few drops of potassium dichromate solu- tion. The use of more than 60 ml. of ammon- ium acetate solution should be avoided. Tkie residue shall be wash
22、ed with distilled water, rinsed with a few ml. of alcohol and ether, dried for approximately 15 minutes at 109 degrees C, plus or minus 5 degrees C., cooled in a desiccator and weighed. The loss in weight ahall be Calculated as the perwntage of lead azide. 4.3.4.3 Antinumy sulF&e. The residue re- ma
23、ining from the lead azide determination shall be extracted with concentrated hydro- chloric acid until free from antimony sulfide. (This extraction can be made without remov- ing the sample from the filtering crucible and thus running the risk of disturbing the as- bestos mat.) Suction shall be appl
24、ied and most of the antimony sulfide extracted with cool concentrated hydrochloric acid, then rinsed thoroughly with hot concentrated hydrochloric MIL-D-46262A (MU) acid, ignited to separate sulphur and organic matter, cooled in a desiccator and weighed. The loss in weight shall be calculated as the
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