PT93307A - PROCESS FOR THE REALIZATION OF ZINC BAROQUE PHOSPHATE COATINGS ON METAL SURFACES - Google Patents
PROCESS FOR THE REALIZATION OF ZINC BAROQUE PHOSPHATE COATINGS ON METAL SURFACES Download PDFInfo
- Publication number
- PT93307A PT93307A PT93307A PT9330790A PT93307A PT 93307 A PT93307 A PT 93307A PT 93307 A PT93307 A PT 93307A PT 9330790 A PT9330790 A PT 9330790A PT 93307 A PT93307 A PT 93307A
- Authority
- PT
- Portugal
- Prior art keywords
- quot
- baroque
- realization
- zinc
- compound
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/34—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing fluorides or complex fluorides
- C23C22/36—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing fluorides or complex fluorides containing also phosphates
- C23C22/367—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing fluorides or complex fluorides containing also phosphates containing alkaline earth metal cations
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
- C23C22/08—Orthophosphates
- C23C22/22—Orthophosphates containing alkaline earth metal cations
Description
í í ' '< *· ''/2, dc ÍÕOS ! 1 } //I 0·-.: ·."·;·, ΟΓ’/Λ J J- -> ^ ./ i u.u «Λ J C & 'j AliC?.0 .- , . \ .1,0 í-w ... :.. ,!vv uú eodnosto ííc >ors:io* rc^jiilcai^-ac- oo ue ^:odo c. fico.:? .x ·„ί.(i.e. ........... 1, 2, 3, 4, 5, 6, 7, 8, (i.e. In addition, The invention relates to a method for the preparation of a compound of formula (I) in which the compound of formula (I) is prepared by the process of the invention. I stay .x · "ί.
0 ?0.3© η » '*· ... . ±,0? 0.3 © η »'* · .... ,
* *_ V/ '3$ fc -* ··-. *K _.«·> K - ‘ * í. 1- ;5 013. x£U3S3 li306 S’Ul?U Gll^íiX 3 L)3. .vai .G-^.1JG;íá ç. ijΌ·:ί C0: _ » f> · * -·. ·-: -.-. _*·· j i../ O/Ol. /0-.......... . . 1- (5-chlorophenyl) -1H-indole-3-carboxylic acid. . i.e., C0: _ »f > · · · ·. (I.e. ............ / 0-
KfKf
UV 5UV 5
'.J G "3 *·* ,~ .i,w :j9J G " 3 *, * .i, w: j9
99
**
UU
O ae e 9 ] u $ r% # " * *» eo:The ae and 9] u $ r% # " * *" it's the:
U- *«." V /*> .O £U- * '. &Quot; V / * > T the
yzzr:sc oi-áosrúczientG, cie seobriu-bo eroi-a ç-ic ,>ela ai Irdo/v/ãc Ce solUçõss aquosas deiOae Co rocfí/uaqtlc·, cut -02L :C.: o u.iencCuliió:i5o iões &ás?io (Π)» s:U;09 ÚC.) a £ol£c:úc, t canados dc conwrc-âo sooro m :.sv£o;l·:· s . OU O-LOSO 0\ 0 -'O* .·-^ •ao /oa? oa -' "-. v:nc ; :orao? aqc, 00000¾ a: 1 OU Q,The aqueous solution is obtained by filtration and the solvent is evaporated to dryness. The aqueous solution is evaporated to dryness. The aqueous solution is evaporated to dryness, filtered, and evaporated to dryness. (Π):: U U i i i i i i i i i i a i i i i i i i i i i i i i i i i i s s s s s s s s. OR O-LOSO 0 \ 0 -'O *. or - '" -. v: nc; Pray? aqc, 00000¾ to: 1 or Q,
Oii-vOOOl^tVOCO, ;\il "00? '•luoõ.o ·' 001'- T*- '0- ' ·; .3 ; fO * ; • ------ % ’·- »/ $ ^3Gitiuo5 diaoacoOr, t - / .. - k.i ±.iju uá/ai c*0 -1/00 » - - - . .0, - í ~ - 0 e/ou í - ·*- elonaoc 0/^0 S · ’ ;_ , : ; . /, aO-VOOO1, tOOCO,; The reaction mixture was stirred for 1 hour. .3; fO *; • - - • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • - .Alpha., .Alpha., .Alpha., .Alpha., .Alpha., .Alpha.,. . /, a
êand
íuG© O f %£/ Α~Α ' »-· ϊ ' » /1 Cg íõgs ζ&ϋεΐΰο·Cg Goadio&eco do oi-oee&so dt •j' -...1' 1' . fOiGíG tio :?oo.l.ísacão-:·ο2τ£·1€ό η»ΛΘ αο ra-rorSidaCgg Í.ÕOGG.C -2 ΐ..;··; o·,- " -Ο·;; Λ - ; d; : (d r Id), o-;.GCeâ·,·,(1). In a preferred embodiment of the present invention, the present invention provides a process for the preparation of a composition according to any one of claims 1 to 4, The invention relates to a process for the preparation of a compound of the formula: ## STR2 ## in which R 2 is as defined in formula (I). o ·, - " -Ο · ;; Λ -; d; : (d r Id), -
} --------4 ^ ~ v>G ::. - - - --* .··. ^ ^ - o tl. e :.e-o-;c..o co.:; ggc. « ·. J- ~ . d C-‘...... ,' ··, 0 :· cor^Gí ! s i - / - d !..· : ;..0 ! - ; =- ev A - ; ' : ..,·.. l=.. ic-..·..· ^ o j <s ' “l * - ·.-. : .«· « .. r .--... . ·- ·. .-·-.-.; Λ. :. c» G ·' .-o ÍGGG idd.Od.GCO} -------- 4 ^ ~ v > G ::. Eur-lex.europa.eu eur-lex.europa.eu . e. ggc. «·. . C-1, ..., (i.e. -; = - ev A -; ...................... Eur-lex.europa.eu eur-lex.europa.eu · · ·. . Λ. :. gt; GGG idd.Od.GCO
GCG :; \ ^ G/ca .* - *r" ‘ ~ G* ’ ->;% f·.- d-^,· . i.j -.____, ·<γ V.-- ’5Γ "Írt O ';'C * *? . ·, U d }'V„ OJO OD r ;CC-d3;GCG:; G / ca. * - * r " (I.e., g). i.j -.____, V V - Γ Γ Γ Í Í Í Í Í V V V V. . O-R-CH3-d3;
Gd'. -G -; >' - ã líCTSrlÇaO G '-.j 'OggGGCG G.-GO£.Gl . - O ,g,gg ...- go„gC ; » 1o3£ 3Í2G>VD( ::), C~:,3 GGGGG ; Gd) 5 c-:·..:.. g:-, -s .1¾.. - d_, ...' l«G tGíGd '. -G-; > ' The invention relates to a method for the preparation of a compound of formula (I). - O, g, g, ..., g "; (1: 3, 32: 32G); Gd), 5 (g)
JÒ.;L dlGCGGJO ..· ; . ... · ; .....GOG,j íiGuGG..'õO !G/ Ovi d'GdC í v CÕGõ GldòiGO o/oa 1 . é 1* i?0JL. . ... ·; .................. is 1 * i? 0
iÕG-ε el,cz/c.oo θ/oc ίο:· eo.cc03õo o? dkd.co Co zdtee. λ ccclicccõo do peoaosso ã-o coozdo • -j ^ jí Zo;ui:dc doccc cc ; ^ oeJo ,;?ddo eco 0. )t G d ffccidcccco rr· W V~ 0/ G / / / / / / / / / / / / / / / / /? dkd.co Co zdtee. The method of claim 1, further comprising the steps of: (a) reacting the compound of formula (I) with the compound of formula (I); (a) (b) and (b).
X XVX XV
V'VC «.» :,..dXv x: u:i d)í V’ i i . - j ; \ ;,· c(D) X is a compound of formula (I). - j; \ ;,· W
, o.·; oofícios cios oolooòootOG pco? oi:L J 0. , : . j . “· : 0:.0 0Ó 05? £ov2r'S*C-pillTSr-Í3C.ÇC.O. ; " 0 00 o .» ooooooo oo iioooneÕb por to oro 30 c· 00 alio π~ o " 0* õo oo:3o/'-2rioaçõo cloro zvs 0 -ooi .00: ' Q C·-’. . Λ ... L‘ Ί... 0- -..j 0U0’ j 0; o: O Vv 00. ... «* .. 0-.: i.:...oooõo O:caooco: oioo Φ - ooo o?"0õooo ...Oo ao. . . ·:·... ·.. .·.. .. . a; «M m» .0: .-·οο“ο óoool:: aOuOiloo. ú.. f o,:0..0 «» .: 0., m* . "0. _ o.ao/oo ., .00: ? ;-Ί·οο: 0 * . .. ....·. ?;· 0...' ·.._. ~ ;* · 0:.v........... 0 00« -.:0 001:10 .... ..0 O .. 4* :1o Ox- ae\j;:37^CL,o .,.- 0 -/ r·· r er, ? 'i s ^ ----a. - t „f L:. / 00000.0¾ 0 <- f» 0 *n·. - · ' , ‘:?o:;::.0* .f fí «- - ... ^ ·. 1 ·-· ^ • τ'.o ·τ .-» C.-0.-’ X l OO .*1« ύ :.ο\ ο ·' -0 -ο,, O.·; What are the benefits of POC? . j. ": 0: .00; C pill-C pill-C pill-C pill-C.OPO Í. ; " 0,00 ooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooo Chloro-2-oxo-3-chloro-2-oxo-2 . Λ ... L 'Ί ... 0 - - ... j 0U0' j 0; oo: VO 00. ... * * 0-: i.:...oooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooooo . . Eur-lex.europa.eu eur-lex.europa.eu The; Â € ‡ â € ‡ â € ‡ â € ‡ â € ‡ â € ‡ â € ‡ â € ‡ â € ‡ â € ‡ (s): o. " 0. . ; -Ί · οο: 0 *. .. ·. (I.e. 0: .v ........... 0 00 «-.:0 001: 10 .... 0 0 4: 37 ° C, 0 ° C, a. . / 00000.0¾ 0 <- f »0 * n ·. Eur-lex.europa.eu eur-lex.europa.eu 1, 2, 3, 4, 5, 6, 7, 8,
; ÚJ ‘ο Γο:.ο-..,.ο ?οο 00.: 10 ·\·. οο.ο ϊ ο: - —: - .. . - . -·Ζ- jOCs ΙΟ Ο 01,- Λ,' • s - Οι..· Ο i Ο 0- '-s c· ..·.. ..-. . ' -“o .... oo: O-OoO. C:2iòÍ@B£i'u-OLOC C ,01 s · . “; Ο Γο: .ο - ..,. Οο οο 00 .: 10 · \ ·. οοο ο ο ο: - -: - ... -. - Ζ Ζ Ζ Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο. . O-O-O. C₂ÍH₂₂N₂O C · C 01 sH₂O: C, "
οαρτβηΐ’ i o *Λ ‘í ri P a •ri vl O «n O CQ r,' Oo © Bo <ri ήooo •B ri 0) Q Λ 43 «í ri 43 © d «* r. 5 ! t ti ri ί 43 Q A ri * ·: ρ ,g ‘Π ri & TJ w ; • í Q O : 1 fí i, © u> ·- -1 f il 5 r*· 43 ri ri O o j; ri "j © " -4 O «1 7> í ri 3 3 oThe title compound was prepared from the title compound as a white solid (0.8 g). 1 H NMR (DMSO-d 6):? 5! , Π Π 43 43 43 43 43 43 43 43 43 43 43 43 43 43 43 43 43 43. TJ w; (I.e. - - - - - - - - - - - - - - - " " -4 '7' respectively.
ίΑ c\ : έ- í l lΑ Α l
f . O - - P ? w* -ri ϊ ri.' ;-j ·. .> Γ ri t- £. 1 · > '--I *·* ; Si D 1 r*J H c-: _ -J·· P O s R O !* O Γ4· ri ri 1 O 53 íi i ri v·* s < 9 -í*; cS 0 0 s 0 i I 0 1 í m •P | 0 t t f t ri I «ri ri j © © © © 0 1 O* ri I *d a 0 'd a 43 I 4» 1 ri <·> rri- n ri '·.:'> O . <: íc 0 • .’3 - ~ Λ_· .' ‘ w 0 .*•1 O -.0 ··; ' 0 ri- 0 ri •P : ) i Ί . V-i Çj C-' O · . , ri *' - j 13 ' Jf. O - - P? w * -ri ϊ ri. ' . . > . 1 · > '- I * · *; If D 1 r * J H c -: - - - • • • • • • • • • • • • • • • • • • • • • • • • • • 9-yl; cS 0 0 s 0 i I 0 1 i m • P | The title compound was prepared from the title compound as a white solid (0.8 g). 1 H NMR (CDCl 3):? In addition, O . <:       '0. (1). V-1. .
Ο tttt - j* i £4 Λ d o i· f. ! í 1 1 5 ! P « π ã í^. • H :: i -P ví § i; *!-> g Çj 'J £ í !r ] •'d V.F 1 f“3 O r*''· P-3 i Q O ij •r-1 0 O £.2 ;! P P. -P : *3 Ί F·^ a 1 2 Cj 6 D í 3 íl s “ * ii d ? s í *.**5 ; P M l . r Jr d P ;- !- ii 3 •i ctí f .: 0 d '·> ç~r ‘-3 d 1» O Câ I rj f Oí P - Í5 tf* Φ i < O ; i f í ç a "d -11 ] r°5 % " ί |- ii ii ·, d 0 3 rj3 í(§ >· 1!2! o P H 1 ;; O rJ r' '5 r*f I ol dl dí lí P 1 di -d , 0 i' "* . C d 6 <- P . ) O i 5 O ΓΡ •" 0 p r . = ! 3 d -'-d c; - -J c r;- 4 V Γ ·“’ c- d.; - j 3 • “2 r td 2 d ·_ © 0 H c • } V> ‘V, P 0 r d d 0 r\ r;·; d r\ 0 :£i P d f4 Ú íc3 h ρ *05 d d & ffí •P ú Vi) N s © <H 43 ntí 1 k o} w (tf O © «H O u 42 s> iá ct5 43 I p“3 í; . Γ"· " c "C« : 75 - . Γ. j . J " rp d : p .p **· . 4 . d '---i *. ·. ' ;· t - r j ; i -P • p p; ’d -Η-'! J c c" ·-* % 5 -i cx UAJ..-C 2Ο tttt - j * i £ 4 Λ d o i · f. ! (11) P? Π? • H :: i -P vi • i; *! - >gt; R < 2 > < / RTI > < / RTI > P-P: 3 3 Ί F a a 1 2 6 D D D D D D D D. . P M l. (d) and (b). (i) a compound of the formula: ## STR1 ## O ; i.e., " d -11] r ° 5% " 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 10, 10, 10, 10, 10, (6) and (5), and (4) 0 p r. =! 3 d -d-c; - - - - - - - - -. - - - - - - - - - - - - - - - - - - - - 'V, P 0 r d d 0 r \ r; ·; d r: * * * * * * * * * * * * * * * * * * * * (c): C: 75 75 f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f Γ f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f f - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1, 2, 3, 4, 5, 6
te* *·» r ’ í.. t-Í^v o U-·- χ> «5 * rí » ** ΓΛ j χ, XV: - H G -.1 ! G r*J f H f «· X- 1 í, .<? , * O H ? v G è *Â O*? *“ -1 H { cj £ j r*á i r- rv. I cH r- 3 - -0 *G -.T· I . 3 í O 3 f4 f #6 3 5 (''X v».-f -Λ λ G H H i .2 O r~j ( --Ϊ - c 01¾ ,χ s V·,} «V Ά ? ’G _ . \ -1 H í' ‘-J G 1 M) H ο «-j «CQ * •'G» r * .; tJ ·* ti * i C j '· . j G-· G * f* | !> .J r4 '> * fJ 1 3 r - 43 * tf* r* í4 Λ } , -G ' - Gò í~. -t G O i ç 3 r*3 V».' i ->, x. i tf» & CJf \í i G *5 f - G \ . í ϊ G rí G/í * l r - Hí 4¾ <F» H · r^ r í •ri O O r3 *d o ttí o *ts$ o <\| --"3 Λ 185 o m •d a â O y € & oí N o d £ a ta OD t3 φ a «ts w «j a •t •H (f, íH v.- - Λ*\ ~V‘ G ;: ' · -» Γ*“ / - V- -ri . O «. - l. ;> r'. Λ *[ -J n = Jr W. /_! a,.- *' 0- ro' O'-'; ·» -d ;5 y·' «.i,» : .. v-dõoO ],C: , . r r do aço (';1.C), ehciyã d: o-o (Γ.ο) e ah&ca Cs aço aisieoda çor iocooõo ατ. ;". aioGoaio^acorfec tiniiao. £id© lia-oas oco: vu... c. ;o:rto . CCS 2-2.2:0 -.d·'! Íleo oa- o*J, .. . dd , o lo να doe coo açoa, fojaa. vov .:.0000,uOOção :iO£Ci?ÍâQ2 0.CÔ-OO ^-..00.,-0 o £ú. 00 via oa foodaáe o;··-- ,, voc^. :: vd‘ Ο 07 Ç» Γ, ..**' 0" ^-v-* .^/ . -«' *a^*- 1 - , . :It. ·· õ-va.JLj -o i <_· ·— / ça- a : ,'V ---.- 9 l>!.: 9 ., -0-ã(1) and (2) and (3). ΓΛ ΓΛ,,,,,,,,,,,,. (1), (2) and (2). , * Or H? v G è * O O *? 1, 2, 3, 4, 5, 6, I-H-3-O-G-T. (S c ¾ s s s s s s s s s s s s s G G G G G G G G G G G G G G G G G G G 1-yl) -benzyl] -2-hydroxy-2-methyl-1H-indol- 1, 2, 3, 4, 5, 6, 8, 9, 10, 12, 13, 13, 13, , wherein R 1, R 2, R 3 and R 4 are as defined in claim 1, wherein R 1 and R 2 are independently selected from the group consisting of: • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • • - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - The steel (1, C), and (b) the steel (1) (Γ ο) and & ah ah a a a aço aço ah ah ah ah ah e e e e e e e e e e e e e e e e e e e e e The invention relates to a process for the preparation of the compounds of the general form of CCS 2-2.2: dd, as the covalent bonds, foley. vc = 0.0000, where: C = O, C = O, C = O; 00 via the food and the; :: vd 'Ο 07 Ç »Γ, .. **' 0 " . - - - - - - - - - - : It. 1, 2, 3, 4, 5, 6, 8, 9, 9
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3906898A DE3906898A1 (en) | 1989-03-03 | 1989-03-03 | ZINC-BARIUM PHOSPHATION OF METAL SURFACES |
Publications (1)
Publication Number | Publication Date |
---|---|
PT93307A true PT93307A (en) | 1990-11-07 |
Family
ID=6375498
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PT93307A PT93307A (en) | 1989-03-03 | 1990-03-01 | PROCESS FOR THE REALIZATION OF ZINC BAROQUE PHOSPHATE COATINGS ON METAL SURFACES |
Country Status (6)
Country | Link |
---|---|
EP (2) | EP0385251A1 (en) |
KR (1) | KR920700308A (en) |
AU (1) | AU5109490A (en) |
DE (2) | DE3906898A1 (en) |
PT (1) | PT93307A (en) |
WO (1) | WO1990010094A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3139795B2 (en) * | 1991-10-29 | 2001-03-05 | 日本パーカライジング株式会社 | Metal surface treatment agent for composite film formation |
JP3417653B2 (en) * | 1994-05-11 | 2003-06-16 | 日本パーカライジング株式会社 | Pretreatment method for painting aluminum material |
KR100317680B1 (en) * | 1999-04-29 | 2001-12-22 | 이계안 | Surface treatment agent for treating aluminium alloy and steel plate simultaneously before painting |
DE10261014B4 (en) * | 2002-12-24 | 2005-09-08 | Chemetall Gmbh | Process for coating metal surfaces with an alkali phosphating solution, aqueous concentrate and use of the metal surfaces coated in this way |
WO2021185449A1 (en) * | 2020-03-19 | 2021-09-23 | Thyssenkrupp Steel Europe Ag | Method for generating a phosphate conversion coating and nickel-free phosphating solution |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3090709A (en) * | 1953-08-10 | 1963-05-21 | Lubrizol Corp | Phosphate coating of metals |
FR1300295A (en) * | 1961-06-22 | 1962-08-03 | Parker Ste Continentale | Phosphating process for rubbing metal surfaces |
DE1184589B (en) * | 1961-06-24 | 1964-12-31 | Metallgesellschaft Ag | Process and means for applying finely crystalline phosphate layers to metal surfaces |
US3104177A (en) * | 1961-12-12 | 1963-09-17 | Lubrizol Corp | Phosphating process |
FR2001032A1 (en) * | 1968-01-31 | 1969-09-19 | Nippon Kokan Kk | |
JPS4824135B1 (en) * | 1968-12-20 | 1973-07-19 | ||
US3676224A (en) * | 1970-10-16 | 1972-07-11 | Lubrizol Corp | Phosphating solution with scale suppressing characteristics |
-
1989
- 1989-03-03 DE DE3906898A patent/DE3906898A1/en not_active Withdrawn
-
1990
- 1990-02-21 KR KR1019900702376A patent/KR920700308A/en not_active Application Discontinuation
- 1990-02-21 AU AU51094/90A patent/AU5109490A/en not_active Abandoned
- 1990-02-21 EP EP90103326A patent/EP0385251A1/en not_active Withdrawn
- 1990-02-21 DE DE90903372T patent/DE59004443D1/en not_active Expired - Fee Related
- 1990-02-21 WO PCT/EP1990/000287 patent/WO1990010094A1/en active IP Right Grant
- 1990-02-21 EP EP90903372A patent/EP0461133B1/en not_active Expired - Lifetime
- 1990-03-01 PT PT93307A patent/PT93307A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
DE3906898A1 (en) | 1990-09-06 |
EP0461133B1 (en) | 1994-01-26 |
KR920700308A (en) | 1992-02-19 |
EP0461133A1 (en) | 1991-12-18 |
EP0385251A1 (en) | 1990-09-05 |
DE59004443D1 (en) | 1994-03-10 |
AU5109490A (en) | 1990-09-26 |
WO1990010094A1 (en) | 1990-09-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ZA200007059B (en) | Epothilone derivatives and their synthesis and use. | |
AU2002357619A1 (en) | Piperazine derivative | |
NZ232601A (en) | Pyrimidine derivatives and use | |
WO1992014716A1 (en) | 2,4-diaminoquinazolines derivatives for enhancing antitumor activity | |
PT93307A (en) | PROCESS FOR THE REALIZATION OF ZINC BAROQUE PHOSPHATE COATINGS ON METAL SURFACES | |
AU769510B2 (en) | Febrifugine and isofebrifugine and processes for the preparation of both | |
Elagamey et al. | Nitriles in Heterocyclic Synthesis. The Reaction of Polyhydric Naphthalenes, 4-Methylcoumarin-3-carbonitrile, and Alkylidenemalononitrile with Methylenemalononitrile. | |
CN100432038C (en) | Method for producing nitrile compound, carboxylic acid compound or carboxylate compound | |
TW200504058A (en) | Method for preparing fused oxazinones | |
KR101428123B1 (en) | Synthesis of 4-amino-pyrimidines | |
DE602004006735D1 (en) | PROCESS FOR THE PREPARATION OF 1,4-DIHYDROPYRIDINE INTERMEDIATES AND THEIR DERIVATIVES | |
Bhat et al. | Triethylamine: an efficient N-base catalyst for synthesis of annulated uracil derivativies in aqueous ethanol | |
DE2730467A1 (en) | BENZYLPYRIMIDINE, METHOD FOR THE PRODUCTION THEREOF, AND MEDICINAL PRODUCTS CONTAINING THE SAME | |
DD287032A5 (en) | PROCESS FOR PREPARING 3-CARBAMOYL-4-ARYL-1,2-DI-HYDRO-ISOCHINOLIN-1H-ONEN | |
KR100211444B1 (en) | Process for producing diacetal | |
Mobinikhaledi et al. | Synthesis of some bicyclic thiazolopyrimidine derivatives | |
Taylor et al. | The hydrolysis of amino groups in certain 2, 4, 5, 6-tetrasubstituted pyrimidines | |
IT8322498A1 (en) | 1- (CYANALKYL) -4-GUANYLPIPERAZINE ACID SALTS, PROCEDURES FOR THEIR PREPARATION AND THEIR USE | |
Lee et al. | Synthesis and in vitro cytotoxicity of 2-alkylaminosubstituted quinoline derivatives | |
AU647082B2 (en) | Process for preparing uracil derivatives | |
DE2643671A1 (en) | 4-PHENYLPIPERIDINYL- AND 4-PHENYLTETRAHYDROPYRIDINYL-ALKYLAMINO-KETOALKANECARBONIC ACIDS AND THEIR SALT WITH ACIDS AND BASES | |
DE1620179A1 (en) | Process for the preparation of new basic derivatives of benzoxazine | |
US3437689A (en) | Aromatic amino acid | |
Baša et al. | Synthesis and transformations of methyl (Z)-2-[(tert-butoxycarbonyl) amino]-3-(dimethylamino) propenoate | |
ANY | Synthesis of Substituted Pyridine, Naphthyridine and Pyrido-Pyrimidine Derivatives |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC3A | Refusal |
Effective date: 19951115 |