ARMY MIL-D-60329-1965 DETONATOR STAB T37 LOADING ASSEMBLING AND PACKING《T37型针刺雷管的装载 组装及包装》.pdf
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1、7- MIL-D-60329 13 7797706 0337675 /- MIL-D=60329(MU) 15 MARCH 1965 MILITARY SPECIFICATION DETONATOR, STAB, T37 LOADING, ASSEMBLING AND PACKING I. SCOPE 1.1 This specification covers the loading, assembling and packing for one type of stab detonator designated as Detonator, Stab, m7. 2. APPLICABLE DO
2、CUMENTS ?.l The following documents of the issue in effect on date of invitation for bids, or request for proposals, form a part of this specification ta the extent specified herein. SPECIFICATIONS MILITARY MILP-116 -P res e r v at i o n , Methods of. aiII6.A-2550 -Ammunition and Spe- cial Weapons,
3、Gen- eral Specification for. MIL-145607 - Inspection Equipment, Supply and Mainte- ItaIlce of. STANDARDS MILITARY : 201. Defeata Method of Code No. %pecth I. (see 6.2) interior coating incomplete .or inadequate Visual O1001 None define . Evidence of poor workmanship (see 3.6) . Visual . AQL 0.66 per
4、cent 01002 . 4.2.2.2 Detonator assembly dwg. 8797794). Mew of . Code No. inspection C the cru- cible and contents shall be placed in a drying oven at 95-105 degrees C. for hour, cooled in a desiccator ,and weighed, The above ex- traction shall b repeated, drying, and weigh- ing with individual 20 ml
5、. portions of chloro- form until the loss in weight on subsequent extractions totals less than 0.003 grams. The loss in weight of the crucible plus contents shall be calculated to percent calcium resi- nate in the sample on a moisture free basis as follows-: Percentage of Calcium Resinate = 100A w w
6、here: A = loss in weight of the crucible plus W = weight of sample. contents. 4.3.2.2 Graphite. The crucible and content remaining after the removal of calcium resi- nate shall be washed with a minimum of three 20 ml. portions of acetone, each por- tion maintained in contact with the residue for app
7、roximately 1 minute with continuous stirring before applying suction, until the aubsequent test for RDX in the acetone washings is negative. The crucible and con- tents shall be washed with a minimum of 3 ml. portions of acetone, each sportion main- tained in contact with the residue for ap- proxima
8、tely 1 minute with continuous stir- ring .before applying suction, until the fol- lowing qualitative test for RDX in the ace- tone washings is negative, The acetone fil- trate shall be transferred to a 25 ml. beaker, evaporaked to dryness on a steam bath and several drops of it solution of chromotro
9、pic acid added in 36N sulfurio acid. The forma- tion of a reddish-brown color, as compared to a pink color obtained by a blank prepared in an identical manner indicates the pres- ence of RDX. The residue shall be aspirated until the odor of acetone is no longer de- tectable; the crucible and content
10、s shall be placed in a drying oven at 95-105 degrees C. for hour, cooled in a desiccator and weighed. The weight of Ithe residue in the crucible shall be calculated to the percentage of graphite in the sample on a moisture free basis as follows : Percentage of Graphite = 100A - w where : A = increas
11、e in weight of filtering cru- cible. W = weight of sample. 4.3.2.3 Total bider-lubrcamt. The per- centage o total binder-lubricant in the sam- ple shall ;be calculated by adding the per- centage of calcium resinate and graphite found. 4.3.3 Moisture content of primer mixture. The moisture content of
12、 the primer mixture shall be determined in accordance with MIL- STD-650 method 101.5 except use a one- gram sample. 4,3.4 Cornpositdon of primer mixture. The composition of the primer mixture shall be determined by performing the following tests in the sequence specified: 4.3.4.1 Barium Nitrate. An
13、accurately weighed portion of approximately 0.5 gram of primer mixture shall be transferred to a tared medium-porosity, fritted glass orucible of 20 ml. capacity. Three ml. of lead azide saturated distilled water shall be added at a temperature of 60 degrees C. plus or minus Provided by IHSNot for R
14、esaleNo reproduction or networking permitted without license from IHS-,-,-_. . - - MIL-D-60329 13 7979906 0337702 1 MILD-60329 (MU) 2 degrees C., agitated for 1 minute, and, if necessary, lumps shall be broken up with a rubber policeman attached to a glass rod. Suction shall be applied. This procedu
15、re shall be reepated five times, making a total of six, 3-mi .extractions. The sample 3n the filtering moible shall be rinsed three times with alcohol, dried in an oven maintained at 60 degrees C, glus or nifnus 5 degrees C. for 30 minutes, cooled in a desiccator and weighed. The loss in weight shal
16、l be calcu- lated as the percentage of barium nitrate in the sample on a dry basis as follows: Barium nitrate, percent = M(A-B) 1-.01M where : A = weight of crucible and sample, B = weight of the crucible and sample after extractions with lead azide saturated water. M = moisture content of sample ob
17、- tained from 4.3.3 in percent. 4.3.4.2 Lead styphnate. 4.3.4.2.1 Basic lead st9phn.de (when apple cable). The residue obtained in the deter- mination of barium nitrate shall be extracted with six-ml. portions of ,saturated ammonium acetate solution at about 25 degrees C., (hot saturated ammonium ac
18、etate shall not be used as it dissolves antimony sulfide :da some extent) agitating each portion for about 30 seconds and allowing each portion to re- main in contact with the residue for approxi- mately 2 minutes. The residue shall be washed with water until the filtrate coming through the crucible
19、 appears colorless. The filtrate and washings shall be quantitatively transferred to a 260 ml. calibrated volumet- ric flask, the beaker washed thoroughly with distilled water and diluted to the mark. Using a calibrated pipette, a 2 ml. aliquot of this solution shall be transferred to a 50 ml. calib
20、rated volumetric flask and diluted to the mark with distilled water. A ,portion of this selection shall be transferred to a corex glass spectrophotometric cell (see 6.5) having a width uf approximately 1 centi- meter (cm.) and its absorbance density de- termined at a wavelength of 410 millimi- crons
21、. As reference, a similar cell containing ammonium acetate solution of the same con- centration as the sample solution shall be used. Since the cell which holds the basic lead styphnate is not identical with the ref- erence cell, the absorbance density obtained ahall be corrected as described above
22、for the difference in the amount of light which the two cells scatter and absorb. To do this, both cells shall be filled with ammonium acetate solution and the absorbance density of the cell which originally contained the basic lead styphnate solution shall be measured at a wavelength of 410 millimi
23、crons. The per- centage of baxic lead styphnate in the Sam- ple shall be calculated on a dry basis as follows : Basic lead styphnate, percent = F (A-B) where: W (1-0lM) D A = optical density of basic lead styph- nate solution. B =optical density of ammonium ace- tate solution. D = width of mrex cell
24、, cm. M =moisture content of sample ob- W = weight of sample. F = Factor rto be determined for each instrument un the basis of a sample of lead styphnate that is suitable for use as a standard. tained from 4.3.3 in percent. 4.3.4.2.2 Determnation of no.)mal lead stgphnate (when applicable). Extract
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