Fine soil generated from the soil washing process can be the second problem, as contaminants are concentrated in the fine soil, and also took the difficult forms to treat because soluble and exchangeable fractions are...Fine soil generated from the soil washing process can be the second problem, as contaminants are concentrated in the fine soil, and also took the difficult forms to treat because soluble and exchangeable fractions are already removed by soil washing process; therefore, the fine soil is indicated to hazardous waste, and discarded in hazardous waste landfill. Thus, this research would be performed that arsenic and heavy metals formed difficult to remove in the fine soil were converted to more treatable fractions with chelating agents. Moreover, feasibility study to apply the second remediation targeted to the fine soil inquired. As a result, the chelating agent was decided 50 mM Na2EDTA, and it could develop the complex. In addition, the result of sequential extraction showed that Mn/Fe-oxide fraction, comprised about 28% of amount at first, was decreased about 16%, and organic fraction, consisted approximately 20%, was also decreased about 11%, while exchangeable fraction and carbonate fraction were increased. This result means that the difficult fractions removed could change fractions） by chelating agent. This research can provide the possibility hazardous waste because of difficulty to remediate. the more treatable fractions （exchangeable and carbonate to treat the fine soil, although the fine soil was regarded to展开更多
The transition-metal-catalyzed copolymerization of olefins with polar comonomers is a direct strategy to access polar-functionalized polyolefins in an economical manner.Due to the intrinsic poisoning effect of polar g...The transition-metal-catalyzed copolymerization of olefins with polar comonomers is a direct strategy to access polar-functionalized polyolefins in an economical manner.Due to the intrinsic poisoning effect of polar groups towards Lewis acidic metal centers and the drastic reactivity differences of polar comonomers versus non-polar olefins,it is challenging to develop catalysts that provide the desired polymer molecular weight,comonomer incorporation,and activity.In this contribution,we tackle this issue from a comonomer perspective using 5,6-disubstituted norbornenes,which are highly versatile,easily accessible,inexpensive,and capable of introducing two functional groups in a single insertion.More importantly,they are only mildly poisoning due to the presence of long spacers between double bonds and polar groups,and are not prone to b-hydride elimination due to their cyclic structures.As strong pdonors,they can competitively bind to metal centers versus olefins.Indeed,phosphine-sulfonate palladium catalysts can catalyze the copolymerization of ethylene with 5,6-disubstituted norbornenes and simultaneously achieve a high polymerization activity,copolymer molecular weight,and comonomer incorporation.The practicality of this system was demonstrated by studying the properties of the resulting polymers,copolymerization in hydrocarbon solvents or in bulk,recovery/utilization of unreacted comonomer,molecular weight modulation,and large-scale synthesis.展开更多
文摘Fine soil generated from the soil washing process can be the second problem, as contaminants are concentrated in the fine soil, and also took the difficult forms to treat because soluble and exchangeable fractions are already removed by soil washing process; therefore, the fine soil is indicated to hazardous waste, and discarded in hazardous waste landfill. Thus, this research would be performed that arsenic and heavy metals formed difficult to remove in the fine soil were converted to more treatable fractions with chelating agents. Moreover, feasibility study to apply the second remediation targeted to the fine soil inquired. As a result, the chelating agent was decided 50 mM Na2EDTA, and it could develop the complex. In addition, the result of sequential extraction showed that Mn/Fe-oxide fraction, comprised about 28% of amount at first, was decreased about 16%, and organic fraction, consisted approximately 20%, was also decreased about 11%, while exchangeable fraction and carbonate fraction were increased. This result means that the difficult fractions removed could change fractions） by chelating agent. This research can provide the possibility hazardous waste because of difficulty to remediate. the more treatable fractions （exchangeable and carbonate to treat the fine soil, although the fine soil was regarded to
基金the National Natural Science Foundation of China(52025031,21690071,U19B6001,and U1904212)K.C.Wong Education Foundation。
文摘The transition-metal-catalyzed copolymerization of olefins with polar comonomers is a direct strategy to access polar-functionalized polyolefins in an economical manner.Due to the intrinsic poisoning effect of polar groups towards Lewis acidic metal centers and the drastic reactivity differences of polar comonomers versus non-polar olefins,it is challenging to develop catalysts that provide the desired polymer molecular weight,comonomer incorporation,and activity.In this contribution,we tackle this issue from a comonomer perspective using 5,6-disubstituted norbornenes,which are highly versatile,easily accessible,inexpensive,and capable of introducing two functional groups in a single insertion.More importantly,they are only mildly poisoning due to the presence of long spacers between double bonds and polar groups,and are not prone to b-hydride elimination due to their cyclic structures.As strong pdonors,they can competitively bind to metal centers versus olefins.Indeed,phosphine-sulfonate palladium catalysts can catalyze the copolymerization of ethylene with 5,6-disubstituted norbornenes and simultaneously achieve a high polymerization activity,copolymer molecular weight,and comonomer incorporation.The practicality of this system was demonstrated by studying the properties of the resulting polymers,copolymerization in hydrocarbon solvents or in bulk,recovery/utilization of unreacted comonomer,molecular weight modulation,and large-scale synthesis.
