NAVY A-A-59491-2000 SEALING COMPOUND THREAD AND GASKET HYDROCARBON FLUID AND WATER RESISTANT《碳化氢液体和防水螺纹垫片密封化合物》.pdf
《NAVY A-A-59491-2000 SEALING COMPOUND THREAD AND GASKET HYDROCARBON FLUID AND WATER RESISTANT《碳化氢液体和防水螺纹垫片密封化合物》.pdf》由会员分享,可在线阅读,更多相关《NAVY A-A-59491-2000 SEALING COMPOUND THREAD AND GASKET HYDROCARBON FLUID AND WATER RESISTANT《碳化氢液体和防水螺纹垫片密封化合物》.pdf(9页珍藏版)》请在麦多课文档分享上搜索。
1、1NOT MEASUREMENT SENSITIVEA-A-59491October 31, 2000COMMERCIAL ITEM DESCRIPTIONSEALING COMPOUND, THREAD AND GASKET, HYDROCARBON FLUID ANDWATER RESISTANTThe General Services Administration has authorized the use of this Commercial ItemDescription, for all federal agencies.1. Abstract. This description
2、 covers requirements for a thread and gasket sealingcompound that is resistant to fuel, engine oils, and water. The compound is aslow-drying black paste, setting into a pliable film; best suited for non-rigid,vibrating semi-permanent and permanent assemblies. It withstands pressures to5000 psi.2. Sa
3、lient characteristics. Salient characteristics shall be in accordance with 2.1through 2.11. Preproduction testing for compIiance with all characteristics thatrequire testing (2.1.1.2, 2.1.2, and 2.2-2.10) shall be performed on the currentformulation and every time there is a formulation change. Prod
4、uction testing ofeach batch for compliance with 2.1.1.2 shall be performed. If tests are required,unless otherwise specified, the sealing compound shall be tested withouttreatment or preconditioning and tests shall be conducted at a temperature of750F 50F and a relative humidity of 50 5 percent.2.1
5、Formulation. The sealing compound shall nominally consist of 50-55 weightpercent clay, 15-20 weight percent rosin, 15-20 weight percent vegetable oil, 10-15 weight percent isopropyl alcohol, and 1-3 weight percent soybean derivative.2.1.1 Detrimental materials.2.1.1.1 Prohibited materials. During th
6、e manufacturing processes, tests, inspections,and storage, mercury or mercury compounds shall not be intentionally added toor come in contact with the product at any time.Beneficial comments, (recommendations, additions, deletions) and any pertinent datawhich may be of use in improving this document
7、 should be addressed to: Commander,Naval Sea Systems Command, ATTN 05Q, 1333 Isaac Hull Avenue SE, Stop 5160,Washington Navy Yard, DC 20376-5160.AMSC N/A FSC 8030DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.Provided by IHSNot for ResaleNo reproduction or networkin
8、g permitted without license from IHS-,-,-A-A-5949122.1.1.2 Chemical impurities. The amount of the following materials in the sealingcompound shall not exceed the limits specified below when tested in accordancewith 2.1.1.3:(a) Halogens shall not exceed 0.0250 weight percent (250 ppm) (g/g) eachof ch
9、lorine, bromine, or fluorine.(b) Total sulfur shall not exceed 0.0250 weight percent (250 ppm)(g/g).(c) Total lead shall not exceed 0.0250 weight percent (250 ppm)(g/g).(d) Total cadmium shall not exceed 0.0250 weight percent (250 ppm)(g/g).2.1.1.3 Chemical impurities Test procedure.(a) Halogen cont
10、ent (consisting of fluorine, chlorine, and bromine) shall bedetermined by decomposing the product using Parr Bomb or Pyrohydrolysis techniques and analysis of the residue by ion chromotography,specific ion electrode, or spectrophotometric methods. Other equivalentmethods may be utilized.(b) Total su
11、lfur content shall be determined by decomposing the productusing Parr Bomb or Pyro hydrolysis techniques and analysis of theresidue by gravimetric or turbidimetric methods. Other equivalentmethods may be utilized.(c) The individual concentrations of lead and cadmium shall be determinedby atomic abso
12、rption, plasma emission, emission spectrographic or X-rayfluorescence methods, as appropriate. Other equivalent methods may beutilized.2.1.2 The sealant shall have been certified and assigned a “Limited” or “Permitted”usage category in accordance with the Nuclear Powered Submarine AtmosphereControl
13、Manual (NAVSEA S9510-AB-ATM-010/(U).2.1.3 The sealant shall not contain any Class I or Class II ozone depleting substancesas designated by the Environmental Protection Agency in Code of FederalRegulations 40 (CFR) Part 82.2.2 Solubility. The solubility of the sealing compound shall be as specified i
14、n table 1when tested in accordance with 2.2.1. and 2.2.2. The aromatic fluid, ethyleneglycol and oil immersion media shall conform to the specifications in table 1. Table 1. SolubilityImmersion media Temperature (0F) % MaximumSolubilityAromatic fluid, ASTM D 471 Reference Fuel D 74 5 10Aromatic flui
15、d, ASTM D 471 Reference Fuel B 74 5 9Ethylene glycol, A-A-870 158 2 5Distilled water 200 5 6ASTM D 471 Oil No. 1 158 2 10ASTM D 471 Oil No. 2 158 2 10ASTM D 471 Oil No. 3 158 2 10Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-A-A-5949132.2.1 Solubil
16、ity - Test panels. Three recessed aluminum panels, conforming to thedesign and measurement of figure 1, shall be used to test the solubility of eachtype of sealing compound in each immersion medium. The test panels shall bedegreased with a suitable degreasing solvent. Care shall be exercised to avoi
17、dskin contact, inhalation, and ingestion of vapors. The panels shall then be placedin an oven at 1580F 20F for 1 hour minimum, cooled in a desiccator for 1 hourminimum, and then weighed to the nearest 1 milligram.2.2.2 Solubility - Test procedure. Each of the fluids in table 1 shall be used separate
18、lyas the immersion medium at the indicated temperatures. The test panels (see2.2.1) shall be filled to the rim of recess with the sealing compound and dried in acirculating air oven for 48 hours at 1580F 20F. After removal from the oven andcooling to room temperature in a desiccator, the specimens s
19、hall be weighed tothe nearest 1 milligram and then immersed for 24 hours minimum in 250 milliliterof the respective fluids. For the aromatic fluids the panels shall be placedhorizontally in the containers to prevent flow of the compounds. For the boilingwater container a reflux condenser is necessar
20、y to prevent loss of water. Allimmersion containers shall be covered to prevent loss of immersion fluid byevaporation. After ethylene glycol immersion, excess glycol shall be removed byimmersing the specimen in water at 740F 50F for 15 minutes minimum. Afterimmersion, the panels immersed in ASTM D 4
21、71 Oil No. 1, ASTM D 471 Oil No.2, and ASTM D 471 Oil No. 3 shall be placed on edge on an absorbent towel forapproximately 30 minutes, turned to the opposite edge for approximately 30minutes to prevent oil residue remaining on the surface. All specimens shall bedried in a circulating air oven at 158
22、0F 20F for 24 hours minimum. Afterremoval from the oven, the specimens shall be cooled to room temperature in adesiccator for 1 hour before weighing. Test panels shall be reweighed.2.2.3 Solubility - Calculation. Percent change in weight shall be calculated as follows:Change in weight, percent = (W1
23、 W2) / (W1-WP) X 100Where:W1 = Weight of the panel and sealing compound before immersion.W2 = Weight of the dried panel and sealing compound after immersion.WP = Weight of panel.2.2.4 Solubility - Report. Results shall be reported as the average of 3 calculations ofpercent change in weight for each
24、type of immersion medium.2.3 Volatile content. The volatile content shall be 13.0 2.0 percent when tested inaccordance with 2.3.1 and 2.3.2.2.3.1 Volatile content - Test panels. Approximately 5 grams of the compound shall beplaced in an accurately weighed to the nearest 1 milligram flat-bottom, meta
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