muster
发表于 2025-3-30 09:57:30
Liquid Cleaning Methods,oducts. Processing and final cleaning of liquids to be used for semiconductor devices is frequently carried out in cleanrooms to provide clean process material for a later operation. Many pharmaceutical products are liquids used for injection or ingestion. Plastic films to be used for photography or
Contend
发表于 2025-3-30 15:58:14
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Feature
发表于 2025-3-30 18:34:12
Surface Cleaning Methods,surfaces are affected by inert and viable particles and by radiation and/or chemical film contamination. They are capable of collecting such materials continuously from any source where they may exist. For that reason, it is necessary that the product surfaces be kept clean and that any potential co
惩罚
发表于 2025-3-30 21:20:13
Standards for Contamination Control Areas,anroom construction and good product fabrication within cleanrooms. Application of the standards permits exchange of definitions and conditions so that a cleanroom design, performance, and operation can be understood in any area as long as it is defined in accordance with accepted standards. The sta
外星人
发表于 2025-3-31 03:24:08
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macabre
发表于 2025-3-31 07:47:46
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和平主义者
发表于 2025-3-31 09:55:31
Cleanroom Design Bases and Allowable Components,nd had been used for fabric or furniture manufacturing. The cleanliness of these building interiors was very poor, and structural components were almost impossible to clean adequately, no matter how much effort was applied. These modified cleanroom areas were modeled after medical and surgical rooms
placebo
发表于 2025-3-31 16:17:07
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表皮
发表于 2025-3-31 18:04:49
Cleanroom Work Support Component Areas,layout of all ancillary and support areas. All items that enter or leave and activities that are carried out in the cleanroom must pass through, are stored in, or are processed in one of these auxiliary support areas. Whenever possible, the support areas are located and maintained out of the cleanro
厚脸皮
发表于 2025-4-1 01:03:48
Cleaning, Maintenance, and Janitorial Needs,cts produced in the cleanroom facility are typically sensitive to material that might be acceptable in other production areas but cannot be allowed in a cleanroom. The extent and frequency of both maintenance and cleaning depend on the cleanroom product or process, as well as its design level. Clean