Processo para a extração com solvente de ions de ferro a partir de soluções aquosas e mistura adequada para a extração com solvente de ions de ferro a partir de soluções aquosas
Aminomethylene phosphinic acid derivs. contg. units of formula (I), soluble in hydrocarbons, or aminomethylene phosphonic acid derivs. contg. units of formula (Ia), or aminomethylene phosphonic acid derivs. of formula R R N-(A-N(R ))pR (II), are used in the extn. of Fe ions from aq. solns. In the fo...
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| description | Aminomethylene phosphinic acid derivs. contg. units of formula (I), soluble in hydrocarbons, or aminomethylene phosphonic acid derivs. contg. units of formula (Ia), or aminomethylene phosphonic acid derivs. of formula R R N-(A-N(R ))pR (II), are used in the extn. of Fe ions from aq. solns. In the formulae: R and R = H, 1-30 C alkyl (opt. carrying up to 15 OH gps. and/or broken by up to 14 non-adjacent O atoms), or 2-30 C alkenyl, 7-18C aralkyl, or 6-14C aryl (opt. substd. with up to 3 1-12C alkyl or alkoxy, halogen, CN, OH or 1-4C alkoxycarbonyl; R -R = H, 1-30 C alkyl (opt. carrying up to 15 OH gps. and/or broken by up to 14 non-adjacent O atoms), 2-30 C alkenyl, 7-18C aralkyl, 6-14C aryl (opt. substd. with up to 3 1-12C alkyl or alkoxy, halogen, CN, OH or 1-4C alkoxycarbonyl), or are gps. of formulae -CR R -PO3H2, -CH2-COOH or -CH2-CH(OH)-R ; at least one of the gps. R -R = -CR R -PO3H2, and at least one other is 6-30C alk(en)yl, 7-18C aralkyl, (substd.) 6-14C aryl or -CH2-CH(OH)-R ; R = 6-30 C alk(en)yl, 7-18C aralkyl or (substd.) 6-14 C aryl; A = 1-12C alkylene (opt. substd. with up to 3 1-30 C alkyl, 2-30C alkenyl, 7-18C aralkyl, or 6-14C aryl, which in their turn may be substd. by up to 3 1-12C alkyl or alkoxy, halogen, CN, OH, or 1-4C alkoxycarbonyl); and p = 0-30,000. Also claimed is a modifier for use in the sepn. of metal ions from aq. solns. by solvent extn.. |
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In the formulae: R and R = H, 1-30 C alkyl (opt. carrying up to 15 OH gps. and/or broken by up to 14 non-adjacent O atoms), or 2-30 C alkenyl, 7-18C aralkyl, or 6-14C aryl (opt. substd. with up to 3 1-12C alkyl or alkoxy, halogen, CN, OH or 1-4C alkoxycarbonyl; R -R = H, 1-30 C alkyl (opt. carrying up to 15 OH gps. and/or broken by up to 14 non-adjacent O atoms), 2-30 C alkenyl, 7-18C aralkyl, 6-14C aryl (opt. substd. with up to 3 1-12C alkyl or alkoxy, halogen, CN, OH or 1-4C alkoxycarbonyl), or are gps. of formulae -CR R -PO3H2, -CH2-COOH or -CH2-CH(OH)-R ; at least one of the gps. R -R = -CR R -PO3H2, and at least one other is 6-30C alk(en)yl, 7-18C aralkyl, (substd.) 6-14C aryl or -CH2-CH(OH)-R ; R = 6-30 C alk(en)yl, 7-18C aralkyl or (substd.) 6-14 C aryl; A = 1-12C alkylene (opt. substd. with up to 3 1-30 C alkyl, 2-30C alkenyl, 7-18C aralkyl, or 6-14C aryl, which in their turn may be substd. by up to 3 1-12C alkyl or alkoxy, halogen, CN, OH, or 1-4C alkoxycarbonyl); and p = 0-30,000. Also claimed is a modifier for use in the sepn. of metal ions from aq. solns. by solvent extn..</description><edition>6</edition><language>por</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; ADHESIVES ; CHEMISTRY ; DYES ; FERROUS OR NON-FERROUS ALLOYS ; MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE ; METALLURGY ; MISCELLANEOUS APPLICATIONS OF MATERIALS ; MISCELLANEOUS COMPOSITIONS ; NATURAL RESINS ; ORGANIC CHEMISTRY ; PAINTS ; POLISHES ; PRETREATMENT OF RAW MATERIALS ; PRODUCTION AND REFINING OF METALS ; TREATMENT OF ALLOYS OR NON-FERROUS METALS</subject><creationdate>1997</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19970812&DB=EPODOC&CC=BR&NR=9508118A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19970812&DB=EPODOC&CC=BR&NR=9508118A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KNUT OPPENLAENDER</creatorcontrib><creatorcontrib>MICHAEL EHLE</creatorcontrib><title>Processo para a extração com solvente de ions de ferro a partir de soluções aquosas e mistura adequada para a extração com solvente de ions de ferro a partir de soluções aquosas</title><description>Aminomethylene phosphinic acid derivs. contg. units of formula (I), soluble in hydrocarbons, or aminomethylene phosphonic acid derivs. contg. units of formula (Ia), or aminomethylene phosphonic acid derivs. of formula R R N-(A-N(R ))pR (II), are used in the extn. of Fe ions from aq. solns. In the formulae: R and R = H, 1-30 C alkyl (opt. carrying up to 15 OH gps. and/or broken by up to 14 non-adjacent O atoms), or 2-30 C alkenyl, 7-18C aralkyl, or 6-14C aryl (opt. substd. with up to 3 1-12C alkyl or alkoxy, halogen, CN, OH or 1-4C alkoxycarbonyl; R -R = H, 1-30 C alkyl (opt. carrying up to 15 OH gps. and/or broken by up to 14 non-adjacent O atoms), 2-30 C alkenyl, 7-18C aralkyl, 6-14C aryl (opt. substd. with up to 3 1-12C alkyl or alkoxy, halogen, CN, OH or 1-4C alkoxycarbonyl), or are gps. of formulae -CR R -PO3H2, -CH2-COOH or -CH2-CH(OH)-R ; at least one of the gps. R -R = -CR R -PO3H2, and at least one other is 6-30C alk(en)yl, 7-18C aralkyl, (substd.) 6-14C aryl or -CH2-CH(OH)-R ; R = 6-30 C alk(en)yl, 7-18C aralkyl or (substd.) 6-14 C aryl; A = 1-12C alkylene (opt. substd. with up to 3 1-30 C alkyl, 2-30C alkenyl, 7-18C aralkyl, or 6-14C aryl, which in their turn may be substd. by up to 3 1-12C alkyl or alkoxy, halogen, CN, OH, or 1-4C alkoxycarbonyl); and p = 0-30,000. Also claimed is a modifier for use in the sepn. of metal ions from aq. solns. by solvent extn..</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>ADHESIVES</subject><subject>CHEMISTRY</subject><subject>DYES</subject><subject>FERROUS OR NON-FERROUS ALLOYS</subject><subject>MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE</subject><subject>METALLURGY</subject><subject>MISCELLANEOUS APPLICATIONS OF MATERIALS</subject><subject>MISCELLANEOUS COMPOSITIONS</subject><subject>NATURAL RESINS</subject><subject>ORGANIC CHEMISTRY</subject><subject>PAINTS</subject><subject>POLISHES</subject><subject>PRETREATMENT OF RAW MATERIALS</subject><subject>PRODUCTION AND REFINING OF METALS</subject><subject>TREATMENT OF ALLOYS OR NON-FERROUS METALS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1997</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqtjTEKwkAURNNYiHoG_wUEgwixVFEsRezDJzuBQJK_2b8r3sfCE1hY52JuwN7GamB4b2acvM9OCqgKWXZMTLh7x_2zfwgV0pBKfUPrQQZUSatDlnBOIhoNX7mhiVSIzgtK3AVRVgI1lfowbBp0gQ3_-WGajEquFbNvTpL58XDdnxawkkMtF2jh891ls15maZptV7-JDywsYhw</recordid><startdate>19970812</startdate><enddate>19970812</enddate><creator>KNUT OPPENLAENDER</creator><creator>MICHAEL EHLE</creator><scope>EVB</scope></search><sort><creationdate>19970812</creationdate><title>Processo para a extração com solvente de ions de ferro a partir de soluções aquosas e mistura adequada para a extração com solvente de ions de ferro a partir de soluções aquosas</title><author>KNUT OPPENLAENDER ; MICHAEL EHLE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_BR9508118A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>por</language><creationdate>1997</creationdate><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</topic><topic>ADHESIVES</topic><topic>CHEMISTRY</topic><topic>DYES</topic><topic>FERROUS OR NON-FERROUS ALLOYS</topic><topic>MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE</topic><topic>METALLURGY</topic><topic>MISCELLANEOUS APPLICATIONS OF MATERIALS</topic><topic>MISCELLANEOUS COMPOSITIONS</topic><topic>NATURAL RESINS</topic><topic>ORGANIC CHEMISTRY</topic><topic>PAINTS</topic><topic>POLISHES</topic><topic>PRETREATMENT OF RAW MATERIALS</topic><topic>PRODUCTION AND REFINING OF METALS</topic><topic>TREATMENT OF ALLOYS OR NON-FERROUS METALS</topic><toplevel>online_resources</toplevel><creatorcontrib>KNUT OPPENLAENDER</creatorcontrib><creatorcontrib>MICHAEL EHLE</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KNUT OPPENLAENDER</au><au>MICHAEL EHLE</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Processo para a extração com solvente de ions de ferro a partir de soluções aquosas e mistura adequada para a extração com solvente de ions de ferro a partir de soluções aquosas</title><date>1997-08-12</date><risdate>1997</risdate><abstract>Aminomethylene phosphinic acid derivs. contg. units of formula (I), soluble in hydrocarbons, or aminomethylene phosphonic acid derivs. contg. units of formula (Ia), or aminomethylene phosphonic acid derivs. of formula R R N-(A-N(R ))pR (II), are used in the extn. of Fe ions from aq. solns. In the formulae: R and R = H, 1-30 C alkyl (opt. carrying up to 15 OH gps. and/or broken by up to 14 non-adjacent O atoms), or 2-30 C alkenyl, 7-18C aralkyl, or 6-14C aryl (opt. substd. with up to 3 1-12C alkyl or alkoxy, halogen, CN, OH or 1-4C alkoxycarbonyl; R -R = H, 1-30 C alkyl (opt. carrying up to 15 OH gps. and/or broken by up to 14 non-adjacent O atoms), 2-30 C alkenyl, 7-18C aralkyl, 6-14C aryl (opt. substd. with up to 3 1-12C alkyl or alkoxy, halogen, CN, OH or 1-4C alkoxycarbonyl), or are gps. of formulae -CR R -PO3H2, -CH2-COOH or -CH2-CH(OH)-R ; at least one of the gps. R -R = -CR R -PO3H2, and at least one other is 6-30C alk(en)yl, 7-18C aralkyl, (substd.) 6-14C aryl or -CH2-CH(OH)-R ; R = 6-30 C alk(en)yl, 7-18C aralkyl or (substd.) 6-14 C aryl; A = 1-12C alkylene (opt. substd. with up to 3 1-30 C alkyl, 2-30C alkenyl, 7-18C aralkyl, or 6-14C aryl, which in their turn may be substd. by up to 3 1-12C alkyl or alkoxy, halogen, CN, OH, or 1-4C alkoxycarbonyl); and p = 0-30,000. Also claimed is a modifier for use in the sepn. of metal ions from aq. solns. by solvent extn..</abstract><edition>6</edition><oa>free_for_read</oa></addata></record> |
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| subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ADHESIVES CHEMISTRY DYES FERROUS OR NON-FERROUS ALLOYS MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE METALLURGY MISCELLANEOUS APPLICATIONS OF MATERIALS MISCELLANEOUS COMPOSITIONS NATURAL RESINS ORGANIC CHEMISTRY PAINTS POLISHES PRETREATMENT OF RAW MATERIALS PRODUCTION AND REFINING OF METALS TREATMENT OF ALLOYS OR NON-FERROUS METALS |
| title | Processo para a extração com solvente de ions de ferro a partir de soluções aquosas e mistura adequada para a extração com solvente de ions de ferro a partir de soluções aquosas |
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