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PL105929B1 - METHOD OF MAKING STABILIZED DUALKYLHYDROXYGLINES - Google Patents

METHOD OF MAKING STABILIZED DUALKYLHYDROXYGLINES Download PDF

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Publication number
PL105929B1
PL105929B1 PL20505178A PL20505178A PL105929B1 PL 105929 B1 PL105929 B1 PL 105929B1 PL 20505178 A PL20505178 A PL 20505178A PL 20505178 A PL20505178 A PL 20505178A PL 105929 B1 PL105929 B1 PL 105929B1
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PL
Poland
Prior art keywords
dualkylhydroxyglines
making stabilized
stabilized
making
lhib
Prior art date
Application number
PL20505178A
Other languages
Polish (pl)
Other versions
PL205051A1 (en
Inventor
Stanislaw Pasynkiewicz
Marek Boleslawski
Andrzej Sadownik
Janusz Serwatowski
Ireneusz Kroenke
Original Assignee
Politechnika Warszawska
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Politechnika Warszawska filed Critical Politechnika Warszawska
Priority to PL20505178A priority Critical patent/PL105929B1/en
Publication of PL205051A1 publication Critical patent/PL205051A1/en
Publication of PL105929B1 publication Critical patent/PL105929B1/en

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Description

OPIS PATENTOWY)H5929 m*^-* &*M&^^ PAJElTSl! PIL Frtent dodatkowy Roszono: 03JD3.78 Paeiirc/eiistHTo: Og^ jpattenaftoKfi optMikarwmmo: 3MMM1 CZYTELNIA Urredu Patentowego PiUt4| lzicz^KH'1'ij Lidm} lat CFL OfWSm — i inihilii2 iKDS«29 JgjlgD jjtv^jk\f^iyzn]i}\k) ^t^ctnmoiiDnaiawe stosuje aif organiczne swiaiM^swieiajaue ttlen, azot, aiaiitec AA ffirifaulktte>w3^^ &wigriki wmtthig \Wvyradlaaifcu v^twaxza sbc jrownl&z guzez wjnowflitaenie JId noztwoiu .zwiazku jlinnwrgi) owsactEse ffl^JU, vwlktarym IRima ^wyz^j podanie anaczenK wns^piazzi^lhS&u vvwcglcwiiliDiowym, mM$y iFtKfliiiwgtmttfj^TTP^usgc^hiiku.w^lowndTiTOiwyTn vwtternpBEgturze rrifee^wyzszej mlz(tffe.PATENT DESCRIPTION) H5929 m * ^ - * & * M & ^^ PAJElTSl! PIL Additional frtent Roszono: 03JD3.78 Paeiirc / eiistHTo: Og ^ jpattenaftoKfi optMikarwmmo: 3MMM1 READING ROOM of Patent Urredu PiUt4 | lzicz ^ KH'1'ij Lidm} years CFL OfWSm - i inihilii2 iKDS «29 JgjlgD jjtv ^ jk \ f ^ iyzn] i} \ k) ^ t ^ ctnmoiiDnaiawe uses aif organic swiaiM ^ swieiajaue oxygen, nitrogen, aiaiiteculktte w3 ^^ & wigriki wmtthig \ Wvyradlaaifcu v ^ twaxza sbc jrownl & z guzez wjnowflitaenie JId nostwoiu .zwiazku jlinnwrgi) owsactEse ffl ^ JU, vwlktarym IRima ^ higher ^ j application anaczenK wnsglKwiiliv ^ lhtp, mwsgltp ^ lhtp ^ lht ^ j .w ^ lowndTiTOiwyTn vwtternpBEgturze rrifee ^ higher mlz (tffe.

JUka jcT^pitszczdlniki weglowodorowe stasuje sie weglowodory adliEatycziie, aromatyczne lhib ua$41icziBL, ltoJte2Ba|towiiia$^ Wipczypadknstosowania iTfT^TWZczahiikówddt^ktronodonDrow^ U : 11 iJCzynnikiBm stabilizujacym ijest sam rozpuszczalnik. Winimdbra liczba czasteczek stdbilizujaayith ukilfljti wynosic.JUka jcT ^ hydrocarbon hydrocarbons are used as adliEatic hydrocarbons, aromatic lhib ua $ 41icziBL, ltoJte2Ba | towiiia $ ^ Wipczyft application of iTfT ^ TWZczahiikówddt ^ ktronodonDrow ^ U: 11 and is a stabilizing factor itself. Winimdbra the number of particles stdbilizujaayith ukilfljti to take.

\W{pEZ$gaadku stosowania in^puszczdlnjkaw \wje#owofliffowydh, stosunek imrilowy IR^^lilD .wody^ymBi 2:: 11 lhib wceaajj aoczynnikiem sstdbiltznj$cymuMad jjst .zwiazek ^lmoo^aniczny ai^jdnjacy ssie \wssioiiow&ku iralkeji \wmadnliaEZfi. Wmimdbra lliczfea uczasteczz^k H^^l st^ilizujacych iiMad vwjynDsi jjtiten.Ww^ntikuBadkeji \wyilztób sne rmwnomdlowa ilosc \woiknu, gazowego lhib Jiidkilego \weglowoiloxu, oso saygndlizm)e skonczenie neskcji.Wydajnosc iprociesu ijestiówna\wydajnoscitteoialycznsj.\ In {pEZ $ gadku of the use of in ^ lmoo ^ vje # owofliffowydh, the imril ratio IR ^^ lilD .water ^ ymBi 2 :: 11 lhib wceaajj the factor sstdbiltznj $ cymuMad jjst. wmadnliaEZfi. Wmimdbra lliczfea participastczz ^ k H ^^ l st ^ ilizujacych iiMad vwjynDsi jjtiten. In ^ ntikuBadkeji \ dream of dream rmwn the number of \ voicemail, gaseous lhib Jiidkilego \ carboniloxu, singularity \ intercommunication, singularity.

BteeLtimiot\\\^dlaz4mije^ IPnawikllaadi U. 1100^ noztworu rtn^mettyioiglinu woeteiae etylowym odcieniu c6#4imwinrik& iili4;211 nasymirego naztwxau \wotty vw asterae deblowym cO/zawaitoM (S0SB4 imdk \wo4y lumieszcza sie wdfooóh oddztólnydi gagjjairmlkflilfa. IRoatwifc tujjjjniflf^lnglfmi \wjgowallzassig dto raeriktoBaiiKftilnilziHKjgoctto ttemjBTatury —#iJiC. fHastecpose (dozuje ssbc sstppniowD noztwor \wnily \waaterae ttik, dby ^paUffiagóie sug crihu iiuzIwdtdw wpu*wffliViflnui railnuti imziwiiui wasly ((jzebl ikraawanffl odkofto £8 jgnflzin)) imniaiiityg mtwymiiye ase {prasz 2 ^wiilfluiiy mii ii«ii||Mi^lm;j» —-TDlC, aiimtjflpllir JJJEBiy liti^l^mi rmicMzaiiti^t jmJlmiHliig ij*mflwwrtiny dlo —44d (C»CBD pawotispe wydziritenie rowiuMntikwwg iikxsn mertanu ((rikdlo 11331)- ©trajnniipe sig (rikrito 114311 mmmmm IPnT^ylkllad in mira 311l (II^ mwitibiMWfltt nrawrt—mi t^p^fa^lirnii V7 ryjii^iiiMiiiiiUiw^TiiiiiJiiiiii^ ^¦wwi«i]lj« s«g „titra 111 (UJ iuimfluw^pj> mifliiiBmmi tos% wtuMfimiuMMiiliwutiriiniMiiiiife wutertcgEEKdMiie ¦-;aft- ffittt^ngjfc ^M*iiiifl*ii^ pk j IH^I3^BEDi^D^BramGnmzS]]l IPnr^^lkSjlJl llllll - TULn Tl 11 Tl nmti^liBiiMSgn iTiMiisHJl«iw»rnii ¦ J^LiiliiiffiBfngjMIiiMMMrffaMPi^jliiiiiiiii mm/ |j|iiiiiig|y[ffl^|liimi^ ^ijprmi—MtifiM ^"^g ^j*TH ^B.^7 nmilOHKEgE) UUMilWilElIl vwdbul^r \W^OIFytolElffi \M^tifrftrTfmBW!r^ilnii!i;jy —fflllJUC- MoS^^O^gC j^ik WJtSZEfj ^il^nmiij jjtt 1 lHiiirfA^^iTn^ tmyymmmtiiiuiiLm Hl^E^fflS^JIlfiJHH^uiiaDsKtlUlDWihi I EPnr^wlkfiafifi K.. Ud Ul lH (ID3 nmscifewis^D mi^Liwjmjii i^ii^ji^iitr^lriMrrtiliiiii^iiniri \wntcfliBEiiHe ^pEDRnOfla a% rilliwiiijl^ 3iffi j3l) [HLMl*N501M li^ftfi^Jlliffl WtltiEilillBIlIL, ^WtttiM^BSEddlllOC —^fflrtS JC, :«llttffii'H^|BffitrilfiiiiiiM TTTM^LiTJijii yai^iniiMJ —¦JMj)1&+9 2. sann zmL9nmiii®niiiiii^ nt^nm, ^e Jb) mnflitwfflmi105929 3 znaczenie, w rozpuszczalniku weglowodorowym wprowadza sie wode rozproszona w rozpuszczalniku weglowodorowym w stosunku molowym 2 : 1 lub wyzszym, w temperaturze nie wyzszej niz 0°C:BteeLtimiot ^ \\\ dlaz4mije IPnawikllaadi ^ U ^ 1100 ^ noztworu rtn mettyioiglinu woeteiae ethyl shade # 4imwinrik c6 &iili4; 211 nasymirego naztwxau \ v wotty asterae doubles Co / zawaitoM (S0SB4 imdk \ wo4y lumieszcza August wdfooóh oddztólnydi gagjjairmlkflilfa. IRoatwifc tujjjjniflf ^ lnglfmi \ wjgowallzassig dto raeriktoBaiiKftilnilziHKjgoctto ttemjBTatury - # iJiC. fHastecpose (metered SSBC sstppniowD noztwor \ wnily \ waaterae ttik, dby ^ paUffiagóie sug crihu iiuzIwdtdw keyway * wffliViflnui railnuti imziwiiui wasly ((jzebl ikraawanffl odkofto £ 8 jgnflzin)) imniaiiityg mtwymiiye ase {prasz 2 R wiilfluiiy mii ii «ii || Mi ^ lm; j» —-TDlC, aiimtjflpllir JJJEBiy liti ^ l ^ mi rmicMzaiiti ^ t jmJlmiHliig ij * mflwwrtiny dlo —44d (C »CBD pawotispe wydziritenie rowiu33xnikwwg © mntikwwg © trajnniipe sig (rikrito 114 311 mmmmm IPnT ^ ylkllad in mira 311l (II ^ mwitibiMWfltt nrawrt — mi t ^ p ^ fa ^ lirnii V7 ryjii ^ iiiMiiiiiUiw ^ TiiiiiJiiiiii ^ ^ ¦wwi «i] lj« s «g i" lj «s. ^ pj> mifliiiBmmi tos% wtuMfimiuMMii liwutiriiniMiiiiife wutertcgEEKdMiie ¦-; aft- ffittt ^ ngjfc ^ M * iiiifl * ii ^ pk j IH ^ I3 ^ BEDi ^ D ^ BramGnmzS]] l IPnr ^^ lkSjlJl llllll - TULn Tl 11 i TULn Tl 11 iw TULn Tln Tl 11 J ^ LiiliiiffiBfngjMIiiMMMrffaMPi ^ jliiiiiiiii mm / | j | iiiiiig | y [ffl ^ | liimi ^ ^ ijprmi — MtifiM ^ "^ g ^ j * TH ^ B. ^ 7 nmilOHKEgE) UUMilWilElIl vwdbul ^ r \ W ^ OIFytol Vwdbul ^ r \ W ^ OIFytol ! r ^ ilnii! i; jy —fflllJUC- MoS ^^ O ^ gC j ^ ik WJtSZEfj ^ il ^ nmiij jjtt 1 lHiiirfA ^^ iTn ^ tmyymmmtiiiuiiLm Hl ^ E ^ fflS ^ JIlfiJHH ^ uiiaDsKtl IUlDrf ^ w KlkjiaDsKtlUlUlDWi Ul lH (ID3 nmscifewis ^ D mi ^ Liwjmjii i ^ ii ^ ji ^ iitr ^ lriMrrtiliiiii ^ iiniri \ wntcfliBEiiHe ^ pEDRnOfla a% rilliwiiijl ^ 3iffi j3l) [HLMlrt * N501M li ^ ftlfi ^ EldlllFi ^EldliffBI ^ JC,: «llttffii'H ^ | BffitrilfiiiiiiM TTTM ^ LiTJijii yai ^ iniiMJ —¦JMj) 1 & + 9 2.sann zmL9nmiii®niiiiii ^ nt ^ nm, ^ e Jb) mnflitwfflmi105929 3 meaning, introduced in a hydrocarbon-based solvent in a hydrocarbon solvent in a molar ratio of 2: 1 or greater, at a temperature not higher than 0 ° C:

PL20505178A 1978-03-03 1978-03-03 METHOD OF MAKING STABILIZED DUALKYLHYDROXYGLINES PL105929B1 (en)

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Application Number Priority Date Filing Date Title
PL20505178A PL105929B1 (en) 1978-03-03 1978-03-03 METHOD OF MAKING STABILIZED DUALKYLHYDROXYGLINES

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Application Number Priority Date Filing Date Title
PL20505178A PL105929B1 (en) 1978-03-03 1978-03-03 METHOD OF MAKING STABILIZED DUALKYLHYDROXYGLINES

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PL205051A1 PL205051A1 (en) 1979-02-26
PL105929B1 true PL105929B1 (en) 1979-11-30

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000037476A1 (en) * 1998-12-19 2000-06-29 Basell Polyolefine Gmbh Method for producing mono-organoboranes or di-organoboranes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000037476A1 (en) * 1998-12-19 2000-06-29 Basell Polyolefine Gmbh Method for producing mono-organoboranes or di-organoboranes

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Publication number Publication date
PL205051A1 (en) 1979-02-26

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