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Towards the design of a zero effluent facility in the pharmaceutical industry

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dc.contributor.author Gouws, JF
dc.contributor.author Majozi, T
dc.date.accessioned 2008-01-17T08:04:38Z
dc.date.available 2008-01-17T08:04:38Z
dc.date.issued 2007-05
dc.identifier.citation Gouws, JF, and Majozi, T. 2007. Towards the design of a zero effluent facility in the pharmaceutical industry. 10th Conference on Process Integration, Modelling and Optimisation for Energy Saving and Pollution Reduction, Ischia Island, Gulf of Naples, 24-27 June 2007, pp. 1-6 en
dc.identifier.uri http://hdl.handle.net/10204/1849
dc.description.abstract One of the main goals of any production facility is to have the least negative effect on the surrounding environment, while still producing the required output. The perfect scenario would be a production facility that produces zero effluents. The pharmaceutical production industry has some unique characteristics that make it possible to reach the goal of zero effluent. In such industries wastewater is generally produced from washing out of mixing vessels. The wastewater thus contains valuable product residue. It is possible, under the correct conditions, to reuse the wastewater as part of the formulation of a subsequent batch of a compatible product, thereby producing zero effluent from the operation. From this the question arises on the design of the production facility as to maximise the opportunity to reuse the wastewater, thus producing zero effluent, and keeping the capital costs of such a plant to a minimum. The derived methodology addresses the design aspect of a zero effluent pharmaceutical facility. The methodology takes storage and scheduling of the pharmaceutical operation into consideration. en
dc.language.iso en en
dc.subject Zero effluent en
dc.subject Batch processing en
dc.subject pharmaceutical production en
dc.title Towards the design of a zero effluent facility in the pharmaceutical industry en
dc.type Conference Presentation en
dc.identifier.apacitation Gouws, J., & Majozi, T. (2007). Towards the design of a zero effluent facility in the pharmaceutical industry. http://hdl.handle.net/10204/1849 en_ZA
dc.identifier.chicagocitation Gouws, JF, and T Majozi. "Towards the design of a zero effluent facility in the pharmaceutical industry." (2007): http://hdl.handle.net/10204/1849 en_ZA
dc.identifier.vancouvercitation Gouws J, Majozi T, Towards the design of a zero effluent facility in the pharmaceutical industry; 2007. http://hdl.handle.net/10204/1849 . en_ZA
dc.identifier.ris TY - Conference Presentation AU - Gouws, JF AU - Majozi, T AB - One of the main goals of any production facility is to have the least negative effect on the surrounding environment, while still producing the required output. The perfect scenario would be a production facility that produces zero effluents. The pharmaceutical production industry has some unique characteristics that make it possible to reach the goal of zero effluent. In such industries wastewater is generally produced from washing out of mixing vessels. The wastewater thus contains valuable product residue. It is possible, under the correct conditions, to reuse the wastewater as part of the formulation of a subsequent batch of a compatible product, thereby producing zero effluent from the operation. From this the question arises on the design of the production facility as to maximise the opportunity to reuse the wastewater, thus producing zero effluent, and keeping the capital costs of such a plant to a minimum. The derived methodology addresses the design aspect of a zero effluent pharmaceutical facility. The methodology takes storage and scheduling of the pharmaceutical operation into consideration. DA - 2007-05 DB - ResearchSpace DP - CSIR KW - Zero effluent KW - Batch processing KW - pharmaceutical production LK - https://researchspace.csir.co.za PY - 2007 T1 - Towards the design of a zero effluent facility in the pharmaceutical industry TI - Towards the design of a zero effluent facility in the pharmaceutical industry UR - http://hdl.handle.net/10204/1849 ER - en_ZA


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