COLLOIDAL AGENTS FOR AQUIFER REMEDIATION
    1.
    发明公开
    COLLOIDAL AGENTS FOR AQUIFER REMEDIATION 有权
    KOLLOIDALE MITTEL ZUR GRUNDWASSERSANIERUNG

    公开(公告)号:EP3027562A4

    公开(公告)日:2017-03-29

    申请号:EP14832703

    申请日:2014-08-01

    摘要: Compositions and methods for treating contaminated soil and/or ground water in situ. The compositions and methods comprise stabilized forms of colloidal activated carbon that are used to quickly sorb contaminants. Unlike traditional activated carbon in granular or powder form, the compounds and methods of the present invention are operative to transport particulate activated carbon through a matrix of soil and groundwater upon application by injection, gravity feed, or percolation into soil and groundwater, which in turn decontaminate groundwater in place without the cost or disruption associated with digging the contaminated soil and groundwater out of the ground for on-site purification or disposal at a hazardous waste landfill.

    摘要翻译: 用于原位处理污染土壤和/或地下水的组合物和方法。 组合物和方法包括用于快速吸附污染物的稳定形式的胶体活性炭。 不同于传统的颗粒状或粉末形式的活性炭,本发明的化合物和方法可用于通过注入,重力进料或渗透到土壤和地下水中的方式将微粒活性炭通过土壤和地下水的基质运输, 对地下水进行净化,无需将受污染的土壤和地下水从地下挖掘造成的相关成本或破坏,用于危险废物填埋场的现场净化或处置。

    BIOSENSOR FOR SMALL MOLECULE ANALYTES
    3.
    发明公开
    BIOSENSOR FOR SMALL MOLECULE ANALYTES 有权
    生物传感器分子小分析物

    公开(公告)号:EP1427821A2

    公开(公告)日:2004-06-16

    申请号:EP02806590.2

    申请日:2002-08-15

    发明人: LAING, Lance, G.

    摘要: A biosensor device for detecting small molecules analytes is provided. The device employs a first class of molecules, e.g., protein that binds to both the analyte and a second class of molecules, e.g., nucleic acid. The binding of the protein to the analyte and nucleic acid can be mutually exclusive, and the presence of analyte in a sample results in a detectable displacement of protein from nucleic acid. Alternatively, binding of the protein to the nucleic acid can depend on the presence of analyte in the sample. In a specific embodiment, either the protein or nucleic acid is immobilized on a solid phase support. An arsenic detection system is exemplified. An ArsR binding sequence from the E. coli ars operon is immobilized on a gold-plated surface. ArsR protein binds to the DNA in the absence of arsenic, and is released in the presence of sodium arsenate or phenylarsine oxide. Protein release results in a change in surface plasmon resonance, and the magnitude or kinetics of the change indicate the concentration of arsenic.

    POLYLACTATE RELEASE COMPOUNDS AND METHODS OF USING SAME
    8.
    发明授权
    POLYLACTATE RELEASE COMPOUNDS AND METHODS OF USING SAME 有权
    化合物用于聚乳酸的使用的释放和方法

    公开(公告)号:EP1044168B1

    公开(公告)日:2003-08-27

    申请号:EP98960177.8

    申请日:1998-11-12

    IPC分类号: C02F1/68 C02F3/00 C08G63/06

    CPC分类号: B09C1/10 C02F1/68 C08G63/06

    摘要: The present invention provides for a family of novel compositions to serve as substrates that release hydroxy acid slowly over time. Preferably the hydroxy acid is an α-hydroxy acid, more preferably it is lactic acid. The compositions are preferably made by reaction of poly(lactic acid) with multifunctional alcohols. Also disclosed are formulations based on the compounds and methods of use for both the compositions and the formulations. The preferred use of the compositions and formulations of the present invention is for bioremediation purposes wherein they provide a time-release source of lactic acid to support the growth and reductive activity of microbes present in a system or medium, such as an aquifer, bioreactor, soil, industrial process, wastestream, body of water, river or well. The microbes destroy or inactivate compounds which are capable of being reduced, such as nitrogen-containing organic compounds, oxygen-containing organic compounds, polyaromatic hydrocarbons, and halogen-containing organic compounds.

    TREATMENT OF AQUIFER MATRIX BACK DIFFUSION
    9.
    发明公开
    TREATMENT OF AQUIFER MATRIX BACK DIFFUSION 审中-公开
    BEHANDLUNG VONGRUNDWASSERLEITERMATRIXRÜCKDIFFUSION

    公开(公告)号:EP3105190A4

    公开(公告)日:2017-09-06

    申请号:EP15748563

    申请日:2015-02-13

    摘要: Compositions and methods for in situ ground water remediation. The compositions comprise a colloidal biomatrix comprised of sorbent particles, such as zeolites, organoclays and activated carbon, dispersed in aqueous solution that are injectable into the permeable zones of an aquifer to be treated. Once deposited into the permeable zones of the aquifer, the groundwater concentrations of contaminants in those zones are depleted, thus increasing the rate of diffusion of contaminants of the less permeable zones. The compositions and methods of the present invention can be used to treat any organic contaminants and provide rapid remediation of contaminated ground water by adsorption and biodegradation of such contaminants.

    摘要翻译: 地下水修复的组成和方法。 该组合物包含胶体生物基质,该胶质生物基质由分散在水溶液中的吸附剂颗粒如沸石,有机粘土和活性炭组成,所述吸附剂颗粒可注射到待处理的含水层的可渗透区中。 一旦沉积到含水层的可渗透区域中,那些区域中的污染物的地下水浓度被耗尽,从而增加了渗透性较差区域的污染物的扩散速率。 本发明的组合物和方法可用于处理任何有机污染物,并通过吸附和生物降解这些污染物来提供污染地下水的快速补救。

    BIOSENSOR FOR SMALL MOLECULE ANALYTES
    10.
    发明授权
    BIOSENSOR FOR SMALL MOLECULE ANALYTES 有权
    生物传感器分子小分析物

    公开(公告)号:EP1427821B1

    公开(公告)日:2007-06-20

    申请号:EP02806590.2

    申请日:2002-08-15

    发明人: LAING, Lance, G.

    摘要: A biosensor device for detecting small molecules analytes is provided. The device employs a first class of molecules, e.g., protein that binds to both the analyte and a second class of molecules, e.g., nucleic acid. The binding of the protein to the analyte and nucleic acid can be mutually exclusive, and the presence of analyte in a sample results in a detectable displacement of protein from nucleic acid. Alternatively, binding of the protein to the nucleic acid can depend on the presence of analyte in the sample. In a specific embodiment, either the protein or nucleic acid is immobilized on a solid phase support. An arsenic detection system is exemplified. An ArsR binding sequence from the E. coli ars operon is immobilized on a gold-plated surface. ArsR protein binds to the DNA in the absence of arsenic, and is released in the presence of sodium arsenate or phenylarsine oxide. Protein release results in a change in surface plasmon resonance, and the magnitude or kinetics of the change indicate the concentration of arsenic.