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Greener Detergents – Gold-Based Catalysts for the Production of Ether

Greener Detergents – Gold-Based Catalysts for the Production of Ether

.Johann 1. Ulf Production Greener .Clariant 2. *

corr. Conclusion Results Experimental Introduction Bundesallee

Prüße

Author: ......     AuPt/CeO scheme Reaction catalyst Optimised   conditions preparation of Variation optimisation Catalyst   

umr aaytcomparison Catalyst Summary Heinrich

Broad tions, Satisfactory Excellent from lyst Optimized ether Non carboxylic Pt Current Here Au/TiO hooctcacid, chloroacetic Produkte aeRnActivity n R name PEG PEG PEG PEG uydgyo butyl + Hexanol Butyldiglykol Genapol Genapol Sapogenat R ‐ 1* ‐ lcl (PEGs), glycols Oxidation orsodn te abxlcacids carboxylic ether corresponding e mrgainmethod impregnation wet CeO uP ratios Au:Pt metal preparation supports 0.1% a ayn ciiybtawy xeln eetvt o a for substrates selectivity of variety excellent broad always but activity Varying

(O & 50, EMail in

, ‐ M M S M toyaeehrcroyi acid carboxylic ether ethoxylate

ionic

mlmin mmol we ‐

Katharina

Pd

2000 carboxylic

no CH

range 38116 2 von 5 methyl 350 0 methyl 500 00methyl 1000 2

+

AuPt(90:10) ssupport as (Deutschland)

LA LA ‐ production

loadings shows

[email protected]

2

show based 7 metal

7 patent

‐ selectivity

T

Thünen

CH ‐

surfactants

1 Detergents Ooctyl EO acids 3 lauryl 030 7 lauryl 070 Ohexyl EO

catalyst g 2 (Al 8 tributylphenyl 080

Me Braunschweig/Germany,

long

of 2 o xdto fvrossubstrates various of oxidation for ‐ fpiayachlfnto fpolyethylene of function primary of 1

) 2 (100:0 methods n

O

a

ether better catalysts leaching

OH 3

‐ via

(0.05 literature ‐ acids new Institut , of

Heidkamp

term

alkyl TiO incomplete

AuPt/CeO ea loading metal

GmbH, active, ‐ process: (>

2

cat/O

0:100) carboxylic environmentally

, –2

such

activity, ‐

which (IW,

‐ Ether 99 AC, stability (vTI), PEGs H~520> 210 ~45 OH

if show wt.

2 84504

‐ %) ‐

‐ ‐ CeO

ceria DP ‐ ‐ ‐

selective

as Institute ‐

rftyakhlehxltsto ethoxylates alkohol fatty or %) 1 belong Williamson’s of

2

‐ R Urea/NaOH, ,

fatty conversion 2

high opt. only

, ‐ Memet

Burgkirchen, under

all (O BaSO is acids HR

‐ ‐

1 9 > 495 ~11 2 4 > 145 ~22 used TEM

62> 2 ~6 745> 495 ~7 31 > 12 ~3 720> 260 ~7 gold

CH

‐ fArclua Technology Agricultural of

2 > 220 2 4 > > 145 375 7 7

130x selectivity alcohol Carboxylic moderate

–Gold

of and to 4

2

the

, accessible ‐ continuous

sound Y CH

‐ optimized

the

as based 2 Aytemir

O as stable

2 wet

and

Germany 3 ) ether support

n ,…)

group catalyst toyae constitute ethoxylates active ‐ 1 ‐

fundamental imp.) O

by selectivity,

but catalysts AuPt/CeO

a ‐ ceria CH

synthesis ‐ by

1 products ‐

of

‐ as flow , Selectivity shows 2 2

‐ opt. Klaus this based

COOH

anionic ‐

a

supported 99 99 99 99 99 99 99 99 99 99

Pt condi

% % % % % % % % % route %

n Biosystems and

‐ still low cata ‐

with

Dieter

and technology ac sur T)Continuous STR) (slurry Batch conditions reaction and Reactors Acids

surfactants. ‐

metal activity ‐

corrosion ecologically

gold

Catalysts

Vorlop the

leaching Me Parameter eetvt 85 Selectivity Activity b a  Long c     ‐ ne piie ecincniin o eao LA070 Genapol for conditions reaction optimized under in

from

platinum Engineering, and

mlmin mmol

second ‐ for ecigsgiiatsalrdcdn no no reduced small significant leaching

Oxidation residence patent eetvt o E 00oiain>9 % analysis 99 TEM > oxidation 1000 M PEG for Selectivity long Good ICP

100

conversion [%] through 1

insufficient b ‐ 20 40 60 80 the , emsaiiysuis(trickle studies stability term

literature ‐ 0 1 questionable Nicolle E analysis OES

g (Heidkamp Me 1020304050600

‐ largest 1 oxidation

catalysts c

...... Batch

0 for ae cats based 0w%T:°C 100 wt% : 10

1

Pt

00rpm 1000 p(O °C 80 (titration) 11 pH catalyst g 25 5–20%substrate size charge g 1000 time fPEG of alformation NaCl comparable ‐ ‐

emsaiiy@vrigcniin o 7days 57 for conditions varying @ stability term

–95 < Schwarz & 2

res. time: 3 min 3 res. time:

class 210 :8bar 8 ): stability

 Pd

for =

%> 34 23

et of ‐

fatty

18 osneigo ea particles metal of sintering no M chlorinated a 

of al.

1000 min, osgiiatmtllahn detected leaching metal significant no Au/TiO

detergents.

2 Eur. due

the

99 toyae and ethoxylates ‐ alcohol

c

pH %> @

time [d] J. 2 to

Lipid c = Parameter: 16

over 0 substrates, AuPt/TiO

ml, 13, =

reaction

flow toyae to ethoxylates 40 99 5

Sci. They ‐

variations

gas c

wt%, oxidation T %>

= = conditions

20–100 6–6000

2 Technol. ‐

can bed)

AuPt/CeO T 57

‐ res. time: 3 min 3 res. time:

°C, ml, lwtrickle flow excess

=

p

flow

60

= 99 81068 be 100°C,

1–30

see and liquid c

%>

oxidized

112

bar, = 24 bar ether

0.06–600

2 use

diagram p: 9

V leaching total 8 bar

p 2010 AuPt/CeO p: =

of

138

= ‐ ml bed 260

opt.

99

18

ml, to

51) V c %

cat

bar, =

2