Enhanced Recovery of Pharmaceutical Solvent driven by EPA Initiative
Enhanced Recovery of Pharmaceutical Solvent driven by EPA Initiative
批准号:
8522808
负责人:
Daniel Campos
金额:
$22.5万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-06-12 至 2016-05-31
关键词:
AcetoneAlcohol consumptionAlcoholsAminesChemicalsCustomDehydrationDrug IndustryEconomicsElectron TransportEnvironmentEnvironmental ImpactEventFamilyFiberFilmGoalsHealthHealth BenefitHeatingHumanIsopropanolKetonesLeadLettersLifeLife Cycle StagesManufacturer NameMarketingMembraneMethanolNamesNaturePermeabilityPharmacologic SubstancePhaseProcessPublic HealthReactionReagentRecoveryRecruitment ActivityRecyclingRelative (related person)ResistanceResourcesRiskSavingsSolidSolutionsSolventsSystemTechnologyUnited States Environmental Protection AgencyWaterWorkbasechemical stabilitycostcost effectiveinnovationinterestmanufacturing processmolecular sievingnovelorganic acidpolyetheretherketonepolysulphonepolyvinylidene fluorideprogramspublic health relevancesuccesswasting
中文摘要
产品说明:近期事件:2011年7月6日,美国环境保护署(EPA)宣布计划为危险的二次材料回收建立新的保障措施,目的是促进回收废物的经济、环境和公共健康效益,重点是几个工业部门,包括制药行业。平均而言,制药商使用至少100公斤的溶剂来生产1公斤的活性药物成分。EPA已经确定,如果用于这些目的的溶剂的产品寿命延长到一次以上,则用作制造和加工助剂的溶剂对环境的影响可以显著降低。通过鼓励安全回收废物,美国环保局希望降低这些废物的生命周期风险。 根据对固体废物定义的这一拟议变更,EPA感兴趣的许多溶剂与水形成混合物,这些混合物难以和/或能量密集,难以用常规分离技术(如蒸馏)分离。高能效、高成本效益和无污染的替代技术将使溶剂回收更加可行。EPA提出的保障措施的净效果是,这些措施将强烈激励制药商回收工艺溶剂。 具体目标:制药行业对使用和回收高纯度溶剂有许多需求。主要用途包括:高纯度醇、开发低成本溶剂脱水的能力以及在温和条件下使溶剂脱水的相对温和且简单的方法。紧凑膜系统(CMS)提出了一种新型膜方法,其可以基于在宽范围(几乎通用)的操作条件下操作的化学惰性无定形全氟膜家族产生极高的脱水速率和高的分离能力。CMS的脱水工艺与现有的制药溶剂(PS)工艺兼容。因此,从化学稳定性的角度来看,它可以与醇、有机酸、酮、胺和非质子溶剂一起操作,仅举几例。由于CMS膜的高通量是基于其高自由体积和全氟性质,因此几乎不需要担心与存在的物质的化学相互作用,并且实际渗透性不会随水活度而显著变化。因此,我们有一个潜在的通用和简单的系统,可以在各种各样的PS上工作,用于各种各样的应用,在不同的水活度。为了增强“通用”PS脱水的潜力,CMS将开发A)具有增强的水/溶剂分离的膜和B)更耐受的系统,其等同于更耐受的多孔载体。CMS已经招募了一些关键公司来供应关键材料,并随后销售最终产品。在第一阶段,CMS将建立一个脱水系统,并证明包括甲醇在内的许多溶剂的脱水。目标是水/甲醇选择性大于15.0。一个平行的目标是与分子筛相比节省50%。
英文摘要
DESCRIPTION: Summary Enhanced Recovery of Pharmaceutical Solvent driven by EPA Initiative Recent Events: On July 6, 2011 the United States Environmental Protection Agency (EPA) announced plans to establish new safeguards for hazardous secondary materials recycling with objectives to promote the economic, environmental, and public health benefits of recycling wastes, with an emphasis on several industrial sectors, including the pharmaceutical industry. On average, pharmaceutical manufacturers use at least 100 kg of solvents to make 1 kg of active pharmaceutical ingredient. EPA has determined that the environmental impacts from solvents used as manufacturing and processing aids could be significantly reduced if the product life of solvents used for these purposes were extended to more than a single use. By encouraging the safe recycling of wastes EPA hopes to reduce the life cycle risk of these wastes. Many of the solvents of interest to the EPA under this proposed change to the solid waste definition form mixtures with water that are difficult and/or energy-intensive to separate with conventional separation technologies such as distillation. Energy-efficient, cost effective, and otherwise non-polluting alternative technologies would make solvent recycling more feasible. The net effect of the EPA proposed safeguards is that these will strongly incentify pharmaceutical manufacturers to recycle process solvents. Specific Aim: There are numerous needs in the pharmaceutical industry to use and recover high purity solvents. Key uses include: high purity alcohol, the ability to develop low-cost dewatering of solvents and a relative gentle and simple process for dewatering solvent under mild conditions. Compact Membrane Systems (CMS) proposes a novel membrane process that can lead to extremely high dewatering rates with high separation capabilities based on a family of chemically inert amorphous perfluoro membranes operating under a wide range (almost universal) of operating conditions. CMS's dewatering process is compatible with existing pharmaceutical solvent (PS) processing. Therefore, from a chemical stability standpoint, it can be operated with alcohols, organic acids, ketones, amines and aprotic solvents, to name a few. Since CMS membrane's high flux is based on its high free volume and perfluoro nature, there is little need for concern about chemical interaction with the species present, and the actual permeability does not change significantly with water activity. Therefore, we have a potentially universal and simple system that can work on a wide range of PS for a wide range of applications under varying water activity. To enhance the potential for "universal" PS dehydration, CMS will develop A) membranes with enhanced water/solvent separation and B) more resistant system which equates to more resistant porous supports. CMS has recruited a number of key companies for supplying key materials and subsequently marketing the final product. During Phase I CMS will build a dehydration system and demonstrate dehydration of a number of solvents including methanol. The goal is water/methanol selectivity greater than 15.0. A parallel goal is 50% savings compared to molecular sieves.
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会议论文
Surface Enhanced Biocompatible Blood Oxygenators
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批准号:7997627
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项目类别:
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资助金额:$12.71万
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财政年份:2010
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负责人:Daniel Campos
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依托单位:
海外基金