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机构地区:[1]上海海顺新型药用包装材料股份有限公司 [2]苏州海顺包装材料有限公司
出 处:《广东包装》2013年第4期31-33,共3页Guangdong Packaging
摘 要:国家药包标准YBB20162012即将实施,新国标对溶剂残留量的要求更严格,要求溶剂残留总量不得超过5Omg/m^2,其中苯类溶剂残留量不得检出,苯类单个溶剂的检出限三0.01mg/m^2。并且检测条件也更严格。药包企业要达到国标,必须从印刷和复合两个环节入手,严格控制溶剂残留。本文详细介绍了无苯印刷技术及无溶剂复合技术的工艺要点以及这两种工艺对于控制溶剂残留的贡献。National standards YBB20162012 is about to implemented, the new national standard for residual solvents requirements is more stringent, requiring total solvent residue shall not exceed the 5.0mg/m^2, including benzene solvent residue can not be detected, the detection limit of single benzene solvent ≤0.01mg/m2. And the test conditions are more stringent. To achieve national standard, the pharmaceutical enterprise need to start with printing and composite, strict control the residual solvent. The article detailed describes the process points of non - benzene printing technology and non-solvent composite technology, it also describes these two processes make the contribution for the residual solvent control.
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