NAVY A-A-59720-2002 SEALING AND LOCKING COMPOUNDS SINGLE-COMPONENT《单元件密封锁闭化合物》.pdf
《NAVY A-A-59720-2002 SEALING AND LOCKING COMPOUNDS SINGLE-COMPONENT《单元件密封锁闭化合物》.pdf》由会员分享,可在线阅读,更多相关《NAVY A-A-59720-2002 SEALING AND LOCKING COMPOUNDS SINGLE-COMPONENT《单元件密封锁闭化合物》.pdf(9页珍藏版)》请在麦多课文档分享上搜索。
1、Beneficial comments, (recommendations, additions, deletions) and any pertinent data which may be of use in improving this document should be addressed to: Commander, Naval Sea Systems Command, ATTN 05Q, 1333 Isaac Hall Avenue SE, STOP 5160, Washington Navy Yard, DC 20376-5160. AMSC N/A FSC 8030 DIST
2、RIBUTION STATEMENT A. Approved for public release; distribution is unlimited. INCH-POUND A-A-59720 October 23, 2002 COMMERCIAL ITEM DESCRIPTION SEALING AND LOCKING COMPOUNDS, SINGLE-COMPONENT The General Services Administration has authorized the use of this Commercial Item Description, for all fede
3、ral agencies. 1. Abstract. This description covers requirements for single-component compounds and their primers suitable for sealing and locking metal parts. The compounds cure to an insoluable state when confined between closely fitting metal surfaces or when applied to surfaces treated with a com
4、patible primer. 2. Salient characteristics. Salient characteristics shall be in accordance with 2.1 through 2.4.2. Preproduction testing for compliance with all characteristics that require testing (2.1.1.2, 2.1.2 and 2.2 through 2.4.2) shall be performed on the current formulation and every time th
5、ere is a formulation change. Production testing of each batch is not required. However, production testing for compliance with 2.1.1.2 shall be performed every four years. Tests shall be conducted as specified on unpolymerized and polymerized compounds and, unless otherwise specified, shall be condu
6、cted at a temperature of 75F +/- 5F and a relative humidity of 50 +/- 5 percent. Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-A-A-59720 2 2.1 Formulation. The locking compounds shall have nominal compositions in accordance with Table 1. Table 1 -
7、Nominal Composition of Locking Compounds and Primer Ingredients Weight Percentage Grades Compound AV Compound AVV Compound HT Primer PR-N Polyglycol dimethacrylate 80-85 60-65 - - Bisphenol A fumerate resin - 30-35 - - Saccharin - 1-3 0.1-1 Cumene Hydroperoxide 5-7 1-3 1-3 - N, N-Dialkytoluidines -
8、0.1-1 0.1-1 - Cellulose Ester 1-3 - - - Polyglycol dioctanoate 1-3 - - - Tributylamine 1-Aromatic dimethacrylate ester - - 75-80 - Maleimide resin - - 10-15 - Hydroxyalkyl methacrylate - - 1-3 - Methyl alcohol - - 1-3 - Silica, amorphous, fumed - - 1-3 - 1-Acetyl-2-phenylhydrazine - - 0.1-1 - Maleic
9、 acid - - 0.1-1 - 2-Ethylhexanoic acid - - - 0.1-1 Organo-copper compound - - - 0.1-1 Trialkylammonium Caboxylate - - - 0.1-1 Acetone - - - 95-100 2.1.1 Detrimental materials. 2.1.1.1 Prohibited materials. During the manufacturing processes, tests, inspections, and storage, mercury or mercury compou
10、nds shall not be intentionally added to or come in contact with the product at any time. 2.1.1.2 Chemical impurities. The amount of the following materials in the locking compound or primer shall not exceed the limits specified below when tested in accordance with 2.1.1.3 in the cured state: (a) Tot
11、al chlorides, bromides and fluorides shall each not exceed 0.0250 weight percent (250 ppm) (g/g). (b) Water leachable sulfur shall not exceed 0.0250 weight percent (250 ppm) (g/g). (c) Total antimony, bismuth, cadmium, lead, tin, zinc and phosphorus shall each not exceed 0.0250 weight percent (250 p
12、pm) (g/g). 2.1.1.3 Chemical impurities Test procedure. 2.1.1.3.1 Halogen content determination. 2.1.1.3.1.1 Halogen content (consisting of fluorine, chlorine, and bromine) shall be determined by decomposing the product using Parr Bomb or Pyro hydrolysis techniques and analysis of the residue by ion
13、chromatography, specific ion electrode, or spectrophotometric methods. Other equivalent methods may be utilized. Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-A-A-59720 3 2.1.1.3.2 Water leachable sulfur test. 2.1.1.3.2.1 The water leaching test sh
14、all be performed as follows: a. Cut one specimen from the selected sample, weighing approximately 15 grams, and record its exact weight to 0.1 gram. The sample weight may be adjusted provided the ratio of sample weight to final volume of solution is maintained (i.e. 15g/500ml). b. Cut the specimen i
15、nto small pieces not greater than 1/4 inch in any dimension. c. Place the specimen in an 800 milliliter (ml) or larger beaker. d. Add approximately 400 ml of distilled water per 15 grams of sample weight to the beaker. e. Cover the beaker with a watch glass and heat for one hour minimum at 200-212F.
16、 f. Allow the beaker to cool to room temperature. g. Vacuum filter the leachate from the beaker separately through a prewashed filter (No. 41 Whatman or equivalent coarse porosity filter) and a Buchner funnel. Wash the beaker thoroughly with distilled water using ten or more washes and vacuum filter
17、 the wash solutions. Dilute the filtrate to 500 ml, or the appropriate volume to maintain a 15 g/500 ml ratio. h. If necessary, store the filtrate in a cleaned polyethylene or glass container covered to prevent evaporation. i. Prepare a control filtrate with no specimen following the instruction in
18、d through h. 2.1.1.3.2.2 Determination of leachable sulfur concentration. Using aliquots from the control filtrate and the sample filtrate in 2.1.1.3.2.1.g, determine the concentration of sulfur as follows: a. Place 25 ml of the filtrate in a 50 ml or larger clean beaker properly identified. b. Add
19、distilled water saturated with bromine drop by drop while stirring until a red-brown color persists. Then cover the beaker with a watch glass. c. Heat the solution in the covered beaker on a hot plate until the bromine color disappears. d. Allow the solution to cool to room temperature. e. Transfer
20、the solution to a volumetric flask and add distilled water rinses from the beaker to make up a final volume that is consistent with the sulfate test method. Determine the sulfate ion concentration of this final diluted volume using an appropriate method of ASTM D 516. f. Use the following formula to
21、 obtain the water-leachable sulfur concentration of the filtrate: Sulfur, g/g (ppm) = C X Vs X V X 0.334/(25.0 X M) Where: C = concentration of sulfate ion (SO42-) in filtrate, in milligrams per liter, determined in step e. Vs= final volume of solution in milliliters per 2.1.1.3.2.1.g V = milliliter
22、s of final diluted volume, and M = grams of the test specimen, prepared per 2.1.1.3.2.1.a 2.1.1.3.2.3 Ion chromatography analysis in accordance with ASTM D 4327 and inductively coupled plasma analysis are acceptable alternates for the ASTM leachate analysis of 2.1.1.3.2.2 specified above. 2.1.1.3.2.
23、4 The leachable sulfur concentration for primer shall be determined by testing the residue that is present after evaporation. The leachable sulfur concentration for compounds shall be determined with material that has been polymerized. 2.1.1.3.3 Analysis for metals and phosphorus 2.1.1.3.3.1 The ind
24、ividual concentrations of antimony, bismuth, cadmium, lead, tin, zinc and phosphorus shall be determined by atomic absorption, plasma emission, emission spectrographic or X-ray fluorescence methods, as appropriate. Other equivalent methods may be utilized. Provided by IHSNot for ResaleNo reproductio
- 1.请仔细阅读文档,确保文档完整性,对于不预览、不比对内容而直接下载带来的问题本站不予受理。
- 2.下载的文档,不会出现我们的网址水印。
- 3、该文档所得收入(下载+内容+预览)归上传者、原创作者;如果您是本文档原作者,请点此认领!既往收益都归您。
下载文档到电脑,查找使用更方便
10000 积分 0人已下载
下载 | 加入VIP,交流精品资源 |
- 配套讲稿:
如PPT文件的首页显示word图标,表示该PPT已包含配套word讲稿。双击word图标可打开word文档。
- 特殊限制:
部分文档作品中含有的国旗、国徽等图片,仅作为作品整体效果示例展示,禁止商用。设计者仅对作品中独创性部分享有著作权。
- 关 键 词:
- NAVYAA597202002SEALINGANDLOCKINGCOMPOUNDSSINGLECOMPONENT 元件 密封 化合物 PDF

链接地址:http://www.mydoc123.com/p-976432.html