{"id":{"repo_id":"plymouth","oai_identifier":"oai:pearl.plymouth.ac.uk:gees-theses-1671"},"canonical_url":"https://search.dev.ndltd.org/etd/plymouth/oai:pearl.plymouth.ac.uk:gees-theses-1671","repository":{"repo_id":"plymouth","name":"University of Plymouth","base_url":"https://pearl.plymouth.ac.uk/do/oai"},"display":{"title":"Mercury species in natural gas condensate","abstract":"The presence of ultra-trace levels of mercury in industrial gas and condensate streams is a cause of both environmental and production concern. The toxic nature of the element, in all forms, together with its ability to shut-down large processing plants dictates a need for its accurate and precise measurement. The study which investigated the recovery of various mercury species, spiked into synthetic and real condensate samples using conventional and new digestion and/or extraction techniques showed recovery was dependent upon the speciation. Using the most efficient technique, L<cysteine with persulphate, recoveries of over 90 % were obtained for diphenyl mercury, ethyl and phenyl mercury chlorides and mercury chloride. The recovery of 15% for the important dimethyl mercury species limits the use of this technique. A novel technique has been developed for the determination of total mercury in complex liquid hydrocarbons. Samples (up to 1.0 ml) were vaporised (400oC) and swept through a gold-coated silica trap maintained at 200°C, which retained all mercury species and discarded the matrix. The trap when heated to 900°C released the mercury for measurement by atomic fluorescence spectrometry (AFS). The recoveries for eight mercury species spiked (10 to 50 ng ml into toluene and condensate were generally over 90 %. The instrumental limit of detection (LOD) was 11 pg. The total mercury content of gas condensates, gasolines and heavy oils were determined. Gas chromatograhy coupled, via a pyrolysis interface, with AF detection was able to determine mercury species in gas condensate, at picogram levels (LOD: 2.5 to 7 pg) using a direct sample injection procedure. For a given column system the positive identification and quantification of up to eight mercury species was obtained. A maximum injector temperature of 125oC was recommended, to avoid the conversion of species. Mass balance calculations show a strong correlation between the total mercury content and the sum of the lower dialkyl mercury species, for all condensate samples studied. Three commercially available mercury removal systems, A, B and C produced a reduction in the mercury content of hydrocarbon streams under pilot plant conditions. The two stage system, 'A', produced a minimum of 30 % conversion from organomercury to elemental mercury after the hydrogenation reaction in stage 1. While elemental mercury was adsorbed by the stage 2 reactor, the organomercury species were not removed. The single stage adsorber 'B' showed 100 % removal efficiency for three dialkyl mercury species in liquid hydrocarbon streams. The removal efficiency for adsorber 'C was species dependent. Two common condensate species gave values of 50 to 80 % removal efficiency while the third species showed time-dependent bleed-off.","abstract_html":"The presence of ultra-trace levels of mercury in industrial gas and condensate streams is a cause of both environmental and production concern. The toxic nature of the element, in all forms, together with its ability to shut-down large processing plants dictates a need for its accurate and precise measurement. The study which investigated the recovery of various mercury species, spiked into synthetic and real condensate samples using conventional and new digestion and/or extraction techniques showed recovery was dependent upon the speciation. Using the most efficient technique, L<cysteine with persulphate, recoveries of over 90 % were obtained for diphenyl mercury, ethyl and phenyl mercury chlorides and mercury chloride. The recovery of 15% for the important dimethyl mercury species limits the use of this technique. A novel technique has been developed for the determination of total mercury in complex liquid hydrocarbons. Samples (up to 1.0 ml) were vaporised (400oC) and swept through a gold-coated silica trap maintained at 200°C, which retained all mercury species and discarded the matrix. The trap when heated to 900°C released the mercury for measurement by atomic fluorescence spectrometry (AFS). The recoveries for eight mercury species spiked (10 to 50 ng ml into toluene and condensate were generally over 90 %. The instrumental limit of detection (LOD) was 11 pg. The total mercury content of gas condensates, gasolines and heavy oils were determined. Gas chromatograhy coupled, via a pyrolysis interface, with AF detection was able to determine mercury species in gas condensate, at picogram levels (LOD: 2.5 to 7 pg) using a direct sample injection procedure. For a given column system the positive identification and quantification of up to eight mercury species was obtained. A maximum injector temperature of 125oC was recommended, to avoid the conversion of species. Mass balance calculations show a strong correlation between the total mercury content and the sum of the lower dialkyl mercury species, for all condensate samples studied. Three commercially available mercury removal systems, A, B and C produced a reduction in the mercury content of hydrocarbon streams under pilot plant conditions. The two stage system, 'A', produced a minimum of 30 % conversion from organomercury to elemental mercury after the hydrogenation reaction in stage 1. While elemental mercury was adsorbed by the stage 2 reactor, the organomercury species were not removed. The single stage adsorber 'B' showed 100 % removal efficiency for three dialkyl mercury species in liquid hydrocarbon streams. The removal efficiency for adsorber 'C was species dependent. Two common condensate species gave values of 50 to 80 % removal efficiency while the third species showed time-dependent bleed-off.","abstract_has_math":false,"creators":["Shafawi, Azman Bin"],"institution":null,"degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1999,"date_issued":"1999-01-01T08:00:00Z","date_published":"1999-01-01T08:00:00Z","updated_at":"2026-07-24T03:49:27Z","subjects":[],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://pearl.plymouth.ac.uk/gees-theses/229","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Shafawi, Azman Bin"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.issued","label":"Date","values":["1999-01-01T08:00:00Z"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://pearl.plymouth.ac.uk/gees-theses/229"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["The presence of ultra-trace levels of mercury in industrial gas and condensate streams is a cause of both environmental and production concern. The toxic nature of the element, in all forms, together with its ability to shut-down large processing plants dictates a need for its accurate and precise measurement. The study which investigated the recovery of various mercury species, spiked into synthetic and real condensate samples using conventional and new digestion and/or extraction techniques showed recovery was dependent upon the speciation. Using the most efficient technique, L<cysteine with persulphate, recoveries of over 90 % were obtained for diphenyl mercury, ethyl and phenyl mercury chlorides and mercury chloride. The recovery of 15% for the important dimethyl mercury species limits the use of this technique. A novel technique has been developed for the determination of total mercury in complex liquid hydrocarbons. Samples (up to 1.0 ml) were vaporised (400oC) and swept through a gold-coated silica trap maintained at 200°C, which retained all mercury species and discarded the matrix. The trap when heated to 900°C released the mercury for measurement by atomic fluorescence spectrometry (AFS). The recoveries for eight mercury species spiked (10 to 50 ng ml into toluene and condensate were generally over 90 %. The instrumental limit of detection (LOD) was 11 pg. The total mercury content of gas condensates, gasolines and heavy oils were determined. Gas chromatograhy coupled, via a pyrolysis interface, with AF detection was able to determine mercury species in gas condensate, at picogram levels (LOD: 2.5 to 7 pg) using a direct sample injection procedure. For a given column system the positive identification and quantification of up to eight mercury species was obtained. A maximum injector temperature of 125oC was recommended, to avoid the conversion of species. Mass balance calculations show a strong correlation between the total mercury content and the sum of the lower dialkyl mercury species, for all condensate samples studied. Three commercially available mercury removal systems, A, B and C produced a reduction in the mercury content of hydrocarbon streams under pilot plant conditions. The two stage system, 'A', produced a minimum of 30 % conversion from organomercury to elemental mercury after the hydrogenation reaction in stage 1. While elemental mercury was adsorbed by the stage 2 reactor, the organomercury species were not removed. The single stage adsorber 'B' showed 100 % removal efficiency for three dialkyl mercury species in liquid hydrocarbon streams. The removal efficiency for adsorber 'C was species dependent. Two common condensate species gave values of 50 to 80 % removal efficiency while the third species showed time-dependent bleed-off."]},{"key":"dc:title","label":"Title","values":["Mercury species in natural gas condensate"]}]}],"canonical_facts":{"dc:creator":["Shafawi, Azman Bin"],"dc:date.issued":["1999-01-01T08:00:00Z"],"dc:description.abstract":["The presence of ultra-trace levels of mercury in industrial gas and condensate streams is a cause of both environmental and production concern. The toxic nature of the element, in all forms, together with its ability to shut-down large processing plants dictates a need for its accurate and precise measurement. The study which investigated the recovery of various mercury species, spiked into synthetic and real condensate samples using conventional and new digestion and/or extraction techniques showed recovery was dependent upon the speciation. Using the most efficient technique, L<cysteine with persulphate, recoveries of over 90 % were obtained for diphenyl mercury, ethyl and phenyl mercury chlorides and mercury chloride. The recovery of 15% for the important dimethyl mercury species limits the use of this technique. A novel technique has been developed for the determination of total mercury in complex liquid hydrocarbons. Samples (up to 1.0 ml) were vaporised (400oC) and swept through a gold-coated silica trap maintained at 200°C, which retained all mercury species and discarded the matrix. The trap when heated to 900°C released the mercury for measurement by atomic fluorescence spectrometry (AFS). The recoveries for eight mercury species spiked (10 to 50 ng ml into toluene and condensate were generally over 90 %. The instrumental limit of detection (LOD) was 11 pg. The total mercury content of gas condensates, gasolines and heavy oils were determined. Gas chromatograhy coupled, via a pyrolysis interface, with AF detection was able to determine mercury species in gas condensate, at picogram levels (LOD: 2.5 to 7 pg) using a direct sample injection procedure. For a given column system the positive identification and quantification of up to eight mercury species was obtained. A maximum injector temperature of 125oC was recommended, to avoid the conversion of species. Mass balance calculations show a strong correlation between the total mercury content and the sum of the lower dialkyl mercury species, for all condensate samples studied. Three commercially available mercury removal systems, A, B and C produced a reduction in the mercury content of hydrocarbon streams under pilot plant conditions. The two stage system, 'A', produced a minimum of 30 % conversion from organomercury to elemental mercury after the hydrogenation reaction in stage 1. While elemental mercury was adsorbed by the stage 2 reactor, the organomercury species were not removed. The single stage adsorber 'B' showed 100 % removal efficiency for three dialkyl mercury species in liquid hydrocarbon streams. The removal efficiency for adsorber 'C was species dependent. Two common condensate species gave values of 50 to 80 % removal efficiency while the third species showed time-dependent bleed-off."],"dc:identifier":["https://pearl.plymouth.ac.uk/gees-theses/229"],"dc:language":["eng"],"dc:title":["Mercury species in natural gas condensate"],"dc:type":["Thesis"]},"updated_at":"2026-07-24T03:49:27Z"}