Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol
Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5%...
Ausführliche Beschreibung
Autor*in: |
Adam, Farook [verfasserIn] |
---|
Format: |
E-Artikel |
---|---|
Sprache: |
Englisch |
Erschienen: |
2015 |
---|
Schlagwörter: |
---|
Umfang: |
9 |
---|
Übergeordnetes Werk: |
Enthalten in: Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity - Bai, Yang ELSEVIER, 2018, an international journal devoted to catalytic science and its applications, Amsterdam [u.a.] |
---|---|
Übergeordnetes Werk: |
volume:489 ; year:2015 ; pages:162-170 ; extent:9 |
Links: |
---|
DOI / URN: |
10.1016/j.apcata.2014.09.047 |
---|
Katalog-ID: |
ELV013255045 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | ELV013255045 | ||
003 | DE-627 | ||
005 | 20230623104156.0 | ||
007 | cr uuu---uuuuu | ||
008 | 180602s2015 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.apcata.2014.09.047 |2 doi | |
028 | 5 | 2 | |a GBVA2015015000011.pica |
035 | |a (DE-627)ELV013255045 | ||
035 | |a (ELSEVIER)S0926-860X(14)00609-7 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
082 | 0 | |a 540 | |
082 | 0 | 4 | |a 540 |q DE-600 |
082 | 0 | 4 | |a 570 |q VZ |
084 | |a 58.11 |2 bkl | ||
100 | 1 | |a Adam, Farook |e verfasserin |4 aut | |
245 | 1 | 0 | |a Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol |
264 | 1 | |c 2015 | |
300 | |a 9 | ||
336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
337 | |a nicht spezifiziert |b z |2 rdamedia | ||
338 | |a nicht spezifiziert |b zu |2 rdacarrier | ||
520 | |a Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction. | ||
650 | 7 | |a Organic–inorgnic hybrid |2 Elsevier | |
650 | 7 | |a tert-Butylation of phenol. |2 Elsevier | |
650 | 7 | |a Immobilization |2 Elsevier | |
650 | 7 | |a MCM-41 |2 Elsevier | |
700 | 1 | |a Kueh, Chien-Wen |4 oth | |
773 | 0 | 8 | |i Enthalten in |n Elsevier Science |a Bai, Yang ELSEVIER |t Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity |d 2018 |d an international journal devoted to catalytic science and its applications |g Amsterdam [u.a.] |w (DE-627)ELV001102958 |
773 | 1 | 8 | |g volume:489 |g year:2015 |g pages:162-170 |g extent:9 |
856 | 4 | 0 | |u https://doi.org/10.1016/j.apcata.2014.09.047 |3 Volltext |
912 | |a GBV_USEFLAG_U | ||
912 | |a GBV_ELV | ||
912 | |a SYSFLAG_U | ||
912 | |a SSG-OLC-PHA | ||
936 | b | k | |a 58.11 |j Mechanische Verfahrenstechnik |q VZ |
951 | |a AR | ||
952 | |d 489 |j 2015 |h 162-170 |g 9 | ||
953 | |2 045F |a 540 |
author_variant |
f a fa |
---|---|
matchkey_str |
adamfarookkuehchienwen:2015----:eeoeeuprpeyaioufnccdiaducinlzdnc4drvdrmieuksslcieool |
hierarchy_sort_str |
2015 |
bklnumber |
58.11 |
publishDate |
2015 |
allfields |
10.1016/j.apcata.2014.09.047 doi GBVA2015015000011.pica (DE-627)ELV013255045 (ELSEVIER)S0926-860X(14)00609-7 DE-627 ger DE-627 rakwb eng 540 540 DE-600 570 VZ 58.11 bkl Adam, Farook verfasserin aut Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol 2015 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction. Organic–inorgnic hybrid Elsevier tert-Butylation of phenol. Elsevier Immobilization Elsevier MCM-41 Elsevier Kueh, Chien-Wen oth Enthalten in Elsevier Science Bai, Yang ELSEVIER Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity 2018 an international journal devoted to catalytic science and its applications Amsterdam [u.a.] (DE-627)ELV001102958 volume:489 year:2015 pages:162-170 extent:9 https://doi.org/10.1016/j.apcata.2014.09.047 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 58.11 Mechanische Verfahrenstechnik VZ AR 489 2015 162-170 9 045F 540 |
spelling |
10.1016/j.apcata.2014.09.047 doi GBVA2015015000011.pica (DE-627)ELV013255045 (ELSEVIER)S0926-860X(14)00609-7 DE-627 ger DE-627 rakwb eng 540 540 DE-600 570 VZ 58.11 bkl Adam, Farook verfasserin aut Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol 2015 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction. Organic–inorgnic hybrid Elsevier tert-Butylation of phenol. Elsevier Immobilization Elsevier MCM-41 Elsevier Kueh, Chien-Wen oth Enthalten in Elsevier Science Bai, Yang ELSEVIER Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity 2018 an international journal devoted to catalytic science and its applications Amsterdam [u.a.] (DE-627)ELV001102958 volume:489 year:2015 pages:162-170 extent:9 https://doi.org/10.1016/j.apcata.2014.09.047 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 58.11 Mechanische Verfahrenstechnik VZ AR 489 2015 162-170 9 045F 540 |
allfields_unstemmed |
10.1016/j.apcata.2014.09.047 doi GBVA2015015000011.pica (DE-627)ELV013255045 (ELSEVIER)S0926-860X(14)00609-7 DE-627 ger DE-627 rakwb eng 540 540 DE-600 570 VZ 58.11 bkl Adam, Farook verfasserin aut Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol 2015 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction. Organic–inorgnic hybrid Elsevier tert-Butylation of phenol. Elsevier Immobilization Elsevier MCM-41 Elsevier Kueh, Chien-Wen oth Enthalten in Elsevier Science Bai, Yang ELSEVIER Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity 2018 an international journal devoted to catalytic science and its applications Amsterdam [u.a.] (DE-627)ELV001102958 volume:489 year:2015 pages:162-170 extent:9 https://doi.org/10.1016/j.apcata.2014.09.047 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 58.11 Mechanische Verfahrenstechnik VZ AR 489 2015 162-170 9 045F 540 |
allfieldsGer |
10.1016/j.apcata.2014.09.047 doi GBVA2015015000011.pica (DE-627)ELV013255045 (ELSEVIER)S0926-860X(14)00609-7 DE-627 ger DE-627 rakwb eng 540 540 DE-600 570 VZ 58.11 bkl Adam, Farook verfasserin aut Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol 2015 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction. Organic–inorgnic hybrid Elsevier tert-Butylation of phenol. Elsevier Immobilization Elsevier MCM-41 Elsevier Kueh, Chien-Wen oth Enthalten in Elsevier Science Bai, Yang ELSEVIER Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity 2018 an international journal devoted to catalytic science and its applications Amsterdam [u.a.] (DE-627)ELV001102958 volume:489 year:2015 pages:162-170 extent:9 https://doi.org/10.1016/j.apcata.2014.09.047 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 58.11 Mechanische Verfahrenstechnik VZ AR 489 2015 162-170 9 045F 540 |
allfieldsSound |
10.1016/j.apcata.2014.09.047 doi GBVA2015015000011.pica (DE-627)ELV013255045 (ELSEVIER)S0926-860X(14)00609-7 DE-627 ger DE-627 rakwb eng 540 540 DE-600 570 VZ 58.11 bkl Adam, Farook verfasserin aut Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol 2015 9 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction. Organic–inorgnic hybrid Elsevier tert-Butylation of phenol. Elsevier Immobilization Elsevier MCM-41 Elsevier Kueh, Chien-Wen oth Enthalten in Elsevier Science Bai, Yang ELSEVIER Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity 2018 an international journal devoted to catalytic science and its applications Amsterdam [u.a.] (DE-627)ELV001102958 volume:489 year:2015 pages:162-170 extent:9 https://doi.org/10.1016/j.apcata.2014.09.047 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 58.11 Mechanische Verfahrenstechnik VZ AR 489 2015 162-170 9 045F 540 |
language |
English |
source |
Enthalten in Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity Amsterdam [u.a.] volume:489 year:2015 pages:162-170 extent:9 |
sourceStr |
Enthalten in Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity Amsterdam [u.a.] volume:489 year:2015 pages:162-170 extent:9 |
format_phy_str_mv |
Article |
bklname |
Mechanische Verfahrenstechnik |
institution |
findex.gbv.de |
topic_facet |
Organic–inorgnic hybrid tert-Butylation of phenol. Immobilization MCM-41 |
dewey-raw |
540 |
isfreeaccess_bool |
false |
container_title |
Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity |
authorswithroles_txt_mv |
Adam, Farook @@aut@@ Kueh, Chien-Wen @@oth@@ |
publishDateDaySort_date |
2015-01-01T00:00:00Z |
hierarchy_top_id |
ELV001102958 |
dewey-sort |
3540 |
id |
ELV013255045 |
language_de |
englisch |
fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV013255045</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230623104156.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180602s2015 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.apcata.2014.09.047</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">GBVA2015015000011.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV013255045</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0926-860X(14)00609-7</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">540</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">570</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">58.11</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Adam, Farook</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2015</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">9</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Organic–inorgnic hybrid</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">tert-Butylation of phenol.</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Immobilization</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">MCM-41</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kueh, Chien-Wen</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier Science</subfield><subfield code="a">Bai, Yang ELSEVIER</subfield><subfield code="t">Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity</subfield><subfield code="d">2018</subfield><subfield code="d">an international journal devoted to catalytic science and its applications</subfield><subfield code="g">Amsterdam [u.a.]</subfield><subfield code="w">(DE-627)ELV001102958</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:489</subfield><subfield code="g">year:2015</subfield><subfield code="g">pages:162-170</subfield><subfield code="g">extent:9</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.apcata.2014.09.047</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">58.11</subfield><subfield code="j">Mechanische Verfahrenstechnik</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">489</subfield><subfield code="j">2015</subfield><subfield code="h">162-170</subfield><subfield code="g">9</subfield></datafield><datafield tag="953" ind1=" " ind2=" "><subfield code="2">045F</subfield><subfield code="a">540</subfield></datafield></record></collection>
|
author |
Adam, Farook |
spellingShingle |
Adam, Farook ddc 540 ddc 570 bkl 58.11 Elsevier Organic–inorgnic hybrid Elsevier tert-Butylation of phenol. Elsevier Immobilization Elsevier MCM-41 Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol |
authorStr |
Adam, Farook |
ppnlink_with_tag_str_mv |
@@773@@(DE-627)ELV001102958 |
format |
electronic Article |
dewey-ones |
540 - Chemistry & allied sciences 570 - Life sciences; biology |
delete_txt_mv |
keep |
author_role |
aut |
collection |
elsevier |
remote_str |
true |
illustrated |
Not Illustrated |
topic_title |
540 540 DE-600 570 VZ 58.11 bkl Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol Organic–inorgnic hybrid Elsevier tert-Butylation of phenol. Elsevier Immobilization Elsevier MCM-41 Elsevier |
topic |
ddc 540 ddc 570 bkl 58.11 Elsevier Organic–inorgnic hybrid Elsevier tert-Butylation of phenol. Elsevier Immobilization Elsevier MCM-41 |
topic_unstemmed |
ddc 540 ddc 570 bkl 58.11 Elsevier Organic–inorgnic hybrid Elsevier tert-Butylation of phenol. Elsevier Immobilization Elsevier MCM-41 |
topic_browse |
ddc 540 ddc 570 bkl 58.11 Elsevier Organic–inorgnic hybrid Elsevier tert-Butylation of phenol. Elsevier Immobilization Elsevier MCM-41 |
format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
format_main_str_mv |
Text Zeitschrift/Artikel |
carriertype_str_mv |
zu |
author2_variant |
c w k cwk |
hierarchy_parent_title |
Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity |
hierarchy_parent_id |
ELV001102958 |
dewey-tens |
540 - Chemistry 570 - Life sciences; biology |
hierarchy_top_title |
Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity |
isfreeaccess_txt |
false |
familylinks_str_mv |
(DE-627)ELV001102958 |
title |
Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol |
ctrlnum |
(DE-627)ELV013255045 (ELSEVIER)S0926-860X(14)00609-7 |
title_full |
Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol |
author_sort |
Adam, Farook |
journal |
Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity |
journalStr |
Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity |
lang_code |
eng |
isOA_bool |
false |
dewey-hundreds |
500 - Science |
recordtype |
marc |
publishDateSort |
2015 |
contenttype_str_mv |
zzz |
container_start_page |
162 |
author_browse |
Adam, Farook |
container_volume |
489 |
physical |
9 |
class |
540 540 DE-600 570 VZ 58.11 bkl |
format_se |
Elektronische Aufsätze |
author-letter |
Adam, Farook |
doi_str_mv |
10.1016/j.apcata.2014.09.047 |
dewey-full |
540 570 |
title_sort |
heterogeneous para-phenylamino sulfonic acid ligand functionalized on mcm-41 derived from rice husk ash: selective mono-alkylated products of tert-butylation of phenol |
title_auth |
Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol |
abstract |
Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction. |
abstractGer |
Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction. |
abstract_unstemmed |
Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction. |
collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA |
title_short |
Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol |
url |
https://doi.org/10.1016/j.apcata.2014.09.047 |
remote_bool |
true |
author2 |
Kueh, Chien-Wen |
author2Str |
Kueh, Chien-Wen |
ppnlink |
ELV001102958 |
mediatype_str_mv |
z |
isOA_txt |
false |
hochschulschrift_bool |
false |
author2_role |
oth |
doi_str |
10.1016/j.apcata.2014.09.047 |
up_date |
2024-07-06T18:25:40.310Z |
_version_ |
1803855163880898560 |
fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV013255045</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230623104156.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180602s2015 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.apcata.2014.09.047</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">GBVA2015015000011.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV013255045</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0926-860X(14)00609-7</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">540</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">570</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">58.11</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Adam, Farook</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Heterogeneous para-phenylamino sulfonic acid ligand functionalized on MCM-41 derived from rice husk ash: Selective mono-alkylated products of tert-butylation of phenol</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2015</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">9</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Highlights • 3-(4-Amino-phenylamino)-propane-1-sulfonic acid was functionalized on MCM-41. • The functionalized material had a high surface area of 468m2 g−1. • The hybrid material was used in the tert-butylation of phenol. • The catalytic alkylation of phenol with tert-butanol (TBA), lead to 99.5% conversion. • XRD showed the structure of MCM-41 remained intact after the catalytic reaction.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Organic–inorgnic hybrid</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">tert-Butylation of phenol.</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Immobilization</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">MCM-41</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Kueh, Chien-Wen</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier Science</subfield><subfield code="a">Bai, Yang ELSEVIER</subfield><subfield code="t">Functionalized rGO as covalent crosslinkers for constructing chemically stable polysulfone-based anion exchange membranes with enhanced ion conductivity</subfield><subfield code="d">2018</subfield><subfield code="d">an international journal devoted to catalytic science and its applications</subfield><subfield code="g">Amsterdam [u.a.]</subfield><subfield code="w">(DE-627)ELV001102958</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:489</subfield><subfield code="g">year:2015</subfield><subfield code="g">pages:162-170</subfield><subfield code="g">extent:9</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.apcata.2014.09.047</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">58.11</subfield><subfield code="j">Mechanische Verfahrenstechnik</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">489</subfield><subfield code="j">2015</subfield><subfield code="h">162-170</subfield><subfield code="g">9</subfield></datafield><datafield tag="953" ind1=" " ind2=" "><subfield code="2">045F</subfield><subfield code="a">540</subfield></datafield></record></collection>
|
score |
7.399637 |