PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 26503005-4 2016 This strain could use BDE-209 as the sole carbon and energy source and degrade 65.1% of BDE-209 (initial concentration being 50 mg/L) within 144 h. To explore the BDE-209 degradation properties of this strain with the co-existed electronic donor, zerovalent iron/activated carbon (ZVI/AC) was introduced to build a microbial-chemical coupling system, which was found to promote the degradation of BDE-209 slightly (74.7% in 144 h). Iron 258-262 homeobox D13 Homo sapiens 88-91 27634155-1 2016 In this study, nanoscale zerovalent iron (NZVI) immobilized on biomass carbon was used for the high efficient removal of BDE 209. Iron 36-40 homeobox D13 Homo sapiens 121-124 26503005-4 2016 This strain could use BDE-209 as the sole carbon and energy source and degrade 65.1% of BDE-209 (initial concentration being 50 mg/L) within 144 h. To explore the BDE-209 degradation properties of this strain with the co-existed electronic donor, zerovalent iron/activated carbon (ZVI/AC) was introduced to build a microbial-chemical coupling system, which was found to promote the degradation of BDE-209 slightly (74.7% in 144 h). Iron 258-262 homeobox D13 Homo sapiens 88-91 26503005-4 2016 This strain could use BDE-209 as the sole carbon and energy source and degrade 65.1% of BDE-209 (initial concentration being 50 mg/L) within 144 h. To explore the BDE-209 degradation properties of this strain with the co-existed electronic donor, zerovalent iron/activated carbon (ZVI/AC) was introduced to build a microbial-chemical coupling system, which was found to promote the degradation of BDE-209 slightly (74.7% in 144 h). Iron 258-262 homeobox D13 Homo sapiens 88-91 26503005-4 2016 This strain could use BDE-209 as the sole carbon and energy source and degrade 65.1% of BDE-209 (initial concentration being 50 mg/L) within 144 h. To explore the BDE-209 degradation properties of this strain with the co-existed electronic donor, zerovalent iron/activated carbon (ZVI/AC) was introduced to build a microbial-chemical coupling system, which was found to promote the degradation of BDE-209 slightly (74.7% in 144 h). Iron 281-284 homeobox D13 Homo sapiens 88-91 26503005-4 2016 This strain could use BDE-209 as the sole carbon and energy source and degrade 65.1% of BDE-209 (initial concentration being 50 mg/L) within 144 h. To explore the BDE-209 degradation properties of this strain with the co-existed electronic donor, zerovalent iron/activated carbon (ZVI/AC) was introduced to build a microbial-chemical coupling system, which was found to promote the degradation of BDE-209 slightly (74.7% in 144 h). Iron 281-284 homeobox D13 Homo sapiens 88-91 26503005-4 2016 This strain could use BDE-209 as the sole carbon and energy source and degrade 65.1% of BDE-209 (initial concentration being 50 mg/L) within 144 h. To explore the BDE-209 degradation properties of this strain with the co-existed electronic donor, zerovalent iron/activated carbon (ZVI/AC) was introduced to build a microbial-chemical coupling system, which was found to promote the degradation of BDE-209 slightly (74.7% in 144 h). Iron 281-284 homeobox D13 Homo sapiens 88-91 25076541-1 2014 An organo-montmorillonite-supported nanoscale zero-valent iron material (M-NZVI) was synthesized to degrade decabromodiphenyl ether (BDE-209). Iron 58-62 homeobox D13 Homo sapiens 133-136 26652203-10 2015 Potential energy surface scans with successive elongation of the Fe-M bonds allow an estimation of the iron-metal bond dissociation energies (BDE) as BDE(Fe-Ni) = 11.3 kcal mol(-1) and BDE(Fe-Pd) = 24.3 kcal mol(-1). Iron 103-107 homeobox D13 Homo sapiens 142-145 26652203-10 2015 Potential energy surface scans with successive elongation of the Fe-M bonds allow an estimation of the iron-metal bond dissociation energies (BDE) as BDE(Fe-Ni) = 11.3 kcal mol(-1) and BDE(Fe-Pd) = 24.3 kcal mol(-1). Iron 103-107 homeobox D13 Homo sapiens 150-153 26652203-10 2015 Potential energy surface scans with successive elongation of the Fe-M bonds allow an estimation of the iron-metal bond dissociation energies (BDE) as BDE(Fe-Ni) = 11.3 kcal mol(-1) and BDE(Fe-Pd) = 24.3 kcal mol(-1). Iron 103-107 homeobox D13 Homo sapiens 150-153 22132821-7 2012 We show, for the first time, that the rate determining barrier for aromatic hydroxylation is proportional to the strength of the O-H bond in the corresponding iron(IV)-hydroxo complex, i.e., BDE(OH), hence this thermochemical property of the oxidant drives the reaction and represents the axial ligand effect. Iron 159-163 homeobox D13 Homo sapiens 191-194 24643388-0 2014 Synergistic degradation of deca-BDE by an enrichment culture and zero-valent iron. Iron 77-81 homeobox D13 Homo sapiens 32-35 24643388-1 2014 Debromination of decabromodiphenyl ether (deca-BDE) by microbe and by zero-valent iron (ZVI) has been reported previously. Iron 82-86 homeobox D13 Homo sapiens 47-50 24643388-1 2014 Debromination of decabromodiphenyl ether (deca-BDE) by microbe and by zero-valent iron (ZVI) has been reported previously. Iron 88-91 homeobox D13 Homo sapiens 47-50 24643388-2 2014 However, no study has indicated the presence of microorganisms and their effect on ZVI-mediated reduction of deca-BDE. Iron 83-86 homeobox D13 Homo sapiens 114-117 24643388-3 2014 Synergistic degradation of deca-BDE by an enrichment culture and ZVI was studied. Iron 65-68 homeobox D13 Homo sapiens 32-35 24643388-6 2014 Correlation analysis also confirmed that ZVI was capable of enhancing microbial population in the debromination of deca-BDE. Iron 41-44 homeobox D13 Homo sapiens 120-123 23856315-3 2013 In this study, the removal processes of decabromodiphenyl ether (BDE-209) and monobromodiphenyl ether (BDE-3) with microscale zerovalent iron (MZVI) were investigated to get better understandings for the removal mechanism based upon adsorption and degradation. Iron 137-141 homeobox D13 Homo sapiens 65-68 23856315-3 2013 In this study, the removal processes of decabromodiphenyl ether (BDE-209) and monobromodiphenyl ether (BDE-3) with microscale zerovalent iron (MZVI) were investigated to get better understandings for the removal mechanism based upon adsorption and degradation. Iron 137-141 homeobox D13 Homo sapiens 103-106 20481499-5 2010 In addition, we have found a correlation for substrate epoxidation reactions catalyzed by a range of heme and nonheme iron(IV)-oxo oxidants with the strength of the O-H bond in the iron-hydroxo complex, i.e. BDE(OH), which is supported by the VB model. Iron 118-122 homeobox D13 Homo sapiens 208-211 20481499-5 2010 In addition, we have found a correlation for substrate epoxidation reactions catalyzed by a range of heme and nonheme iron(IV)-oxo oxidants with the strength of the O-H bond in the iron-hydroxo complex, i.e. BDE(OH), which is supported by the VB model. Iron 181-185 homeobox D13 Homo sapiens 208-211 32798868-3 2020 The objective of this research was to study microbial redox cycles of iron in ZVI oxidation and deca-brominated diphenyl ether (deca-BDE) removal. Iron 70-74 homeobox D13 Homo sapiens 133-136 32798868-9 2020 ZVI oxidation activity by IORB only increased to 13.14% and 37.0% in the absence and presence of deca-BDE, respectively. Iron 0-3 homeobox D13 Homo sapiens 102-105 32798868-12 2020 Deca-BDE significantly influenced the effects of iron-metabolizing microorganisms on ZVI oxidation by altering the composition of microbial communities. Iron 49-53 homeobox D13 Homo sapiens 5-8 32798868-12 2020 Deca-BDE significantly influenced the effects of iron-metabolizing microorganisms on ZVI oxidation by altering the composition of microbial communities. Iron 85-88 homeobox D13 Homo sapiens 5-8 29778810-3 2018 Here we reported the debromination pathways of three BDE congeners (BDE-21, 25 and 29) by nano-zerovalent iron (n-ZVI). Iron 106-110 homeobox D13 Homo sapiens 53-56 29778810-3 2018 Here we reported the debromination pathways of three BDE congeners (BDE-21, 25 and 29) by nano-zerovalent iron (n-ZVI). Iron 106-110 homeobox D13 Homo sapiens 68-71 29778810-6 2018 Singly occupied molecular orbitals of BDE anions are well correlated with their actual debromination pathways, which successfully explain why these BDE congeners exhibit certain debromination pathways in n-ZVI system. Iron 206-209 homeobox D13 Homo sapiens 38-41 29778810-6 2018 Singly occupied molecular orbitals of BDE anions are well correlated with their actual debromination pathways, which successfully explain why these BDE congeners exhibit certain debromination pathways in n-ZVI system. Iron 206-209 homeobox D13 Homo sapiens 148-151 29778810-7 2018 In addition, microscale zerovalent zinc (m-ZVZ), iron-based bimetals (Fe/Ag and Fe/Pd) were also used to debrominate PBDEs, with BDE-21 as target pollutant. Iron 49-53 homeobox D13 Homo sapiens 118-121 21469227-6 2011 Furthermore, the axial ligand of the oxidant influences the pK(a) value of the iron(IV)-oxo group, and, as a consequence, the bond dissociation energy (BDE(OH) value correlates with the barrier height for the reverse sulfoxidation reaction. Iron 79-83 homeobox D13 Homo sapiens 152-155