Industrial organic chemistry:
Gespeichert in:
| Hauptverfasser: | , |
|---|---|
| Format: | Buch |
| Sprache: | German English |
| Veröffentlicht: |
Weinheim
VCH
1997
|
| Ausgabe: | 3., completely rev. ed. |
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | Dt. Ausg. u.d.T.: Weissermel, Klaus: Industrielle organische Chemie |
| Beschreibung: | XVII, 464 S. graph. Darst. |
| ISBN: | 3527288384 |
Internformat
MARC
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| 240 | 1 | 0 | |a Industrielle organische Chemie |
| 245 | 1 | 0 | |a Industrial organic chemistry |c Klaus Weissermel ; Hans-Jürgen Arpe |
| 250 | |a 3., completely rev. ed. | ||
| 264 | 1 | |a Weinheim |b VCH |c 1997 | |
| 300 | |a XVII, 464 S. |b graph. Darst. | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 500 | |a Dt. Ausg. u.d.T.: Weissermel, Klaus: Industrielle organische Chemie | ||
| 650 | 4 | |a Chemistry, organic | |
| 650 | 7 | |a Tecnologia quimica |2 larpcal | |
| 650 | 4 | |a Chemistry, Organic | |
| 650 | 4 | |a Chemistry, Technical | |
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Datensatz im Suchindex
| _version_ | 1807229809347002368 |
|---|---|
| adam_text |
CONTENTS
1.
VARIOUS
ASPECTS
OF
THE
ENERGY
AND
RAW
MATERIAL
SUPPLY
.
1
1.1.
PRESENT
AND
PREDICTABLE
ENERGY
REQUIREMENTS
.
2
1.2.
AVAILABILITY
OF
INDIVIDUAL
SOURCES
.
3
1.2.1.
OIL
.
3
1.2.2.
NATURAL
GAS
.
4
1.2.3.
COAL
.
5
1.2.4.
NUCLEAR
FUELS
.
5
1.3.
PROSPECTS
FOR
THE
FUTURE
ENERGY
SUPPLY
.
7
1.4.
PRESENT
AND
ANTICIPATED
RAW
MATERIAL
SITUATION
.
8
1.4.1.
PETROCHEMICAL
PRIMARY
PRODUCTS
.
8
1.4.2.
COAL
CONVERSION
PRODUCTS
.
11
2.
BASIC
PRODUCTS
OF
INDUSTRIAL
SYNTHESES
.
13
2.1.
SYNTHESIS
GAS
.
13
2.1.1.
GENERATION
OF
SYNTHESIS
GAS
.
13
2.1.1.1.
SYNTHESIS
GAS
VIA
COAL
GASIFICATION
.
14
2.1.1.2.
SYNTHESIS
GAS
VIA
CRACKING
OF
NATURAL
GAS
AND
OIL
.
17
2.1.2.
SYNTHESIS
GAS
PURIFICATION
AND
USE
.
19
2.2.
PRODUCTION
OF
THE
PURE
SYNTHESIS
GAS
COMPONENTS
.
21
2.2.1.
CARBON
MONOXIDE
.
21
2.2.2.
HYDROGEN
.
24
2.3.
CI-UNITS
.
27
2.3.1.
METHANOL
.
27
2.3.1.1.
MANUFACTURE
OF
METHANOL
.
28
2.3.1.2.
APPLICATIONS
AND
POTENTIAL
APPLICATIONS
OF
METHANOL
.
30
2.3.2.
FORMALDEHYDE
.
35
2.3.2.1.
FORMALDEHYDE
FROM
METHANOL
.
36
2.3.2.2.
USES
AND
POTENTIAL
USES
OF
FORMALDEHYDE
.
38
2.3.3.
FORMIC
ACID
.
40
2.3.4.
HYDROCYANIC
ACID
.
44
2.3.5.
METHYLAMINES
.
49
2.3.6.
HALOGEN
DERIVATIVES
OF
METHANE
.
50
2.3.6.1.
CHLOROMETHANES
.
50
2.3.6.2.
CHLOROFLUOROMETHANES
.
55
XII
CONTENTS
3.
OLEFINS
.
59
3.1.
HISTORICAL
DEVELOPMENT
OF
OLEFIN
CHEMISTRY
.
59
3.2.
OLEFINS
VIA
CRACKING
OF
HYDROCARBONS
.
59
3.3.
SPECIAL
MANUFACTURING
PROCESSES
FOR
OLEFINS
.
63
3.3.1.
ETHYLENE,
PROPENE
.
63
3.3.2.
BUTENES
.
66
3.3.3.
HIGHER
OLEFINS
.
74
3.3.3.1.
UNBRANCHED
HIGHER
OLEFINS
.
75
3.3.3.2.
BRANCHED
HIGHER
OLEFINS
.
83
3.4.
OLEFIN
METATHESIS
.
85
4.
ACETYLENE
.
91
4.1.
PRESENT
SIGNIFICANCE
OF
ACETYLENE
.
91
4.2.
MANUFACTURING
PROCESSES
FOR
ACETYLENE
.
93
4.2.1.
MANUFACTURE
BASED
ON
CALCIUM
CARBIDE
.
93
4.2.2.
THERMAL
PROCESSES
.
94
4.3.
UTILIZATION
OF
ACETYLENE
.
98
5.
1,3-DIOLEFINS
.
105
5.1.
1,3-BUTADIENE
.
105
5.1.1.
TRADITIONAL
SYNTHESES
OF
1,3-BUTADIENE
.
106
5.1.2.
1,3-BUTADIENE
FROM
C
4
CRACKING
FRACTIONS
.
107
5.1.3.
1,3-BUTADIENE
FROM
C
4
ALKANES
AND
ALKENES
.
109
5.1.4.
UTILIZATION
OF
1,3-BUTADIENE
.
112
5.2.
ISOPRENE
.
115
5.2.1.
ISOPRENE
FROM
C
5
CRACKING
FRACTIONS
.
115
5.2.2.
ISOPRENE
FROM
SYNTHETIC
REACTIONS
.
117
5.3.
CHLOROPRENE
.
120
5.4.
CYCLOPENTADIENE
.
123
6.
SYNTHESES
INVOLVING
CARBON
MONOXIDE
.
125
6.1.
HYDROFORMYLATION
OF
OLEFINS
.
125
6.1.1.
THE
CHEMICAL
BASIS
OF
HYDROFORMYLATION
.
126
6.1.2.
INDUSTRIAL
OPERATION
OF
HYDROFORMYLATION
.
129
6.1.3.
CATALYST
MODIFICATIONS
IN
HYDROFORMYLATION
.
132
6.1.4.
UTILIZATION
OF
'
OXO
'
PRODUCTS
.
134
6.1.4.1,
'
OXO
'
ALCOHOLS
.
134
6.I.4.2.
'
OXO
'
CARBOXYLIC
ACIDS
.
136
6.1.4.3.
ALDOL
AND
CONDENSATION
PRODUCTS
OF
THE
'
OXO
'
ALDEHYDES
.
137
6.2.
CARBONYLATION
OF
OLEFINS
.
139
6.3.
THE
KOCH
CARBOXYLIC
ACID
SYNTHESIS
.
141
CONTENTS
XIII
7.
OXIDATION
PRODUCTS
OF
ETHYLENE
.
143
7.1.
ETHYLENE
OXIDE
.
143
7.1.1.
ETHYLENE
OXIDE
BY
CHLOROHYDRIN
PROCESS
.
144
7.1.2.
ETHYLENE
OXIDE
BY
DIRECT
OXIDATION
.
144
7.1.2.1.
CHEMICAL
PRINCIPLES
.
144
7.1.2.2.
PROCESS
OPERATION
.
146
7.1.2.3.
POTENTIAL
DEVELOPMENTS
IN
ETHYLENE
OXIDE
MANUFACTURE
.
148
7.2.
SECONDARY
PRODUCTS
OF
ETHYLENE
OXIDE
.
149
7.2.1.
ETHYLENE
GLYCOL
AND
HIGHER
ETHYLENE
GLYCOLS
.
150
7.2.1.1.
POTENTIAL
DEVELOPMENTS
IN
ETHYLENE
GLYCOL
MANUFACTURE
.
151
7.2.1.2.
USES
OF
ETHYLENE
GLYCOL
.
153
7.2.1.3.
SECONDARY
PRODUCTS
-
GLYOXAL,
DIOXOLANE,
1,4-DIOXANE
.
154
7.2.2.
POLYETHOXYLATES
.
156
7.2.3.
ETHANOLAMINES
AND
SECONDARY
PRODUCTS
.
157
7.2.4.
ETHYLENE
GLYCOL
ETHERS
.
160
7.2.5.
ADDITIONAL
PRODUCTS
FROM
ETHYLENE
OXIDE
.
162
7.3.
ACETALDEHYDE
.
163
7.3.1.
ACETALDEHYDE
VIA
OXIDATION
OF
ETHYLENE
.
164
7.3.1.1.
CHEMICAL
BASIS
.
164
7.3.1.2.
PROCESS
OPERATION
.
166
7.3.2.
ACETALDEHYDE
FROM
ETHANOL
.
167
7.3.3.
ACETALDEHYDE
BY
C
3
/C4
ALKANE
OXIDATION
.
168
7.4.
SECONDARY
PRODUCTS
OF
ACETALDEHYDE
.
169
7.4.1.
ACETIC
ACID
.
169
7.4.1.1.
ACETIC
ACID
BY
OXIDATION
OF
ACETALDEHYDE
.
170
7.4.I.2.
ACETIC
ACID
BY
OXIDATION
OF
ALKANES
AND
ALKENES
.
172
7.4.1.3.
CARBONYLATION
OF
METHANOL
TO
ACETIC
ACID
.
175
7.4.1.4.
POTENTIAL
DEVELOPMENTS
IN
ACETIC
ACID
MANUFACTURE
.
177
7.4.1.5.
USES
OF
ACETIC
ACID
.
178
7.4.2.
ACETIC
ANHYDRIDE
AND
KETENE
.
180
7.4.3.
ALDOL
CONDENSATION
OF
ACETALDEHYDE
AND
SECONDARY
PRODUCTS
.
184
7.4.4.
ETHYL
ACETATE
.
186
7.4.5.
PYRIDINE
AND
ALKYLPYRIDINES
.
188
8.
ALCOHOLS
.
191
8.1.
LOWER
ALCOHOLS
.
191
8.1.1.
ETHANOL
.
191
8.1.2.
ISOPROPANOL
.
196
8.1.3.
BUTANOLS
.
199
8.1.4.
AMYL
ALCOHOLS
.
203
8.2.
HIGHER
ALCOHOLS
.
203
8.2.1.
OXIDATION
OF
PARAFFINS
TO
ALCOHOLS
.
207
8.2.2.
ALFOL
SYNTHESIS
.
208
XIV
CONTENTS
8.3.
POLYHYDRIC
ALCOHOLS
.
210
8.3.1.
PENTAERYTHRITOL
.
210
8.3.2.
TRIMETHYLOLPROPANE
.
211
8.3.3.
NEOPENTYL
GLYCOL
.
212
9.
VINYL-HALOGEN
AND
VINYL-OXYGEN
COMPOUNDS
.
215
9.1.
VINYL-HALOGEN
COMPOUNDS
.
215
9.1.1. VINYL
CHLORIDE
.
215
9.1.1.1.
VINYL
CHLORIDE
FROM
ACETYLENE
.
216
9.1.1.2.
VINYL
CHLORIDE
FROM
ETHYLENE
.
217
9.1.1.3.
POTENTIAL
DEVELOPMENTS
IN
VINYL
CHLORIDE
MANUFACTURE
.
220
9.1.1.4.
USES
OF
VINYL
CHLORIDE
AND
1
,2-DICHLOROETHANE
.
221
9.1.2.
VINYLIDENE
CHLORIDE
.
223
9.1.3. VINYL
FLUORIDE
AND
VINYLIDENE
FLUORIDE
.
223
9.1.4.
TRICHLORO-AND
TETRACHLOROETHYLENE
.
225
9.1.5.
TETRAFLUOROETHYLENE
.
227
9.2.
VINYL
ESTERS
AND
ETHERS
.
228
9.2.1.
VINYL
ACETATE
.
228
9.2.1.1. VINYL
ACETATE
BASED
ON
ACETYLENE
OR
ACETALDEHYDE
.
228
9.2.1.2.
VINYL
ACETATE
BASED
ON
ETHYLENE
.
229
9.2.1.3.
POSSIBILITIES
FOR
DEVELOPMENT
OF
VINYL
ACETATE
MANUFACTURE
.
233
9.2.2. VINYL
ESTERS
OF
HIGHER
CARBOXYLIC
ACIDS
.
234
9.2.3.
VINYL
ETHERS
.
235
10.
COMPONENTS
FOR
POLYAMIDES
.
237
10.1.
DICARBOXYLIC
ACIDS
.
238
10.1.1.
ADIPIC
ACID
.
239
10.1.2.
1,12-DODECANEDIOIC
ACID
.
243
10.2.
DIAMINES
AND
AMINOCARBOXYLIC
ACIDS
.
244
10.2.1.
HEXAMETHYLENEDIAMINE
.
244
10.2.1.1.
MANUFACTURE
OF
ADIPONITRILE
.
245
10.2.1.2.
HYDROGENATION
OF
ADIPONITRILE
.
249
10.2.1.3.
POTENTIAL
DEVELOPMENTS
IN
ADIPONITRILE
MANUFACTURE
.
250
10.2.2.
CO-AMINOUNDECANOIC
ACID
.
250
10.3.
LACTAMS
.
251
10.3.1.
E-CAPROLACTAM
.
251
10.3.1.1.
E-CAPROLACTAM
FROM
THE
CYCLOHEXANONE
OXIME
ROUTE
.
252
10.3.1.2.
ALTERNATIVE
MANUFACTURING
PROCESSES
FOR
E-CAPROLACTAM
.
256
10.3.1.3.
POSSIBILITIES
FOR
DEVELOPMENT
IN
E-CAPROLACTAM
MANUFACTURE
.
258
10.3.1.4.
USES
OF
E-CAPROLACTAM
.
260
10.3.2.
LAURYL
LACTAM
.
262
CONTENTS
XV
11.
PROPENE
CONVERSION
PRODUCTS
.
265
11.1.
OXIDATION
PRODUCTS
OF
PROPENE
.
266
11.1.1.
PROPYLENE
OXIDE
.
266
11.1.1.1.
PROPYLENE
OXIDE
FROM
THE
CHLOROHYDRIN
PROCESS
.
266
11.1.1.2.
INDIRECT
OXIDATION
ROUTES
TO
PROPYLENE
OXIDE
.
267
11.1.1.3.
POSSIBILITIES
FOR
DEVELOPMENT
IN
THE
MANUFACTURE
OF
PROPYLENE
OXIDE
.
271
11.1.2.
SECONDARY
PRODUCTS
OF
PROPYLENE
OXIDE
.
275
11.1.3.
ACETONE
.
276
11.1.3.1.
DIRECT
OXIDATION
OF
PROPENE
.
277
11.1.3.2.
ACETONE
FROM
ISOPROPANOL
.
278
11.1.4.
SECONDARY
PRODUCTS
OF
ACETONE
.
279
11.1.4.1.
ACETONE
ALDOLIZATION
AND
SECONDARY
PRODUCTS
.
280
11.1.4.2.
METHACRYLIC
ACID
AND
ESTER
.
281
11.1.5.
ACROLEIN
.
285
11.1.6.
SECONDARY
PRODUCTS
OF
ACROLEIN
.
287
11.1.7.
ACRYLIC
ACID
AND
ESTERS
.
289
11.1.7.1.
TRADITIONAL
ACRYLIC
ACID
MANUFACTURE
.
289
11.1.7.2.
ACRYLIC
ACID
FROM
PROPENE
.
291
11.1.7.3.
POSSIBILITIES
FOR
DEVELOPMENT
IN
ACRYLIC
ACID
MANUFACTURE
.
293
11.2.
ALLYL
COMPOUNDS
AND
SECONDARY
PRODUCTS
.
294
11.2.1.
ALLYL
CHLORIDE
.
294
11.2.2.
ALLYL
ALCOHOL
AND
ESTERS
.
297
11.2.3.
GLYCEROL
FROM
ALLYL
PRECURSORS
.
299
11.3.
ACRYLONITRILE
.
302
11.3.1.
TRADITIONAL
ACRYLONITRILE
MANUFACTURE
.
303
11.3.2.
AMMOXIDATION
OF
PROPENE
.
304
11.3.2.1.
SOHIO
ACRYLONITRILE
PROCESS
.
305
11.3.2.2.
OTHER
PROPENE/PROPANE
AMMOXIDATION
PROCESSES
.
306
11.3.3.
POSSIBILITIES
FOR
DEVELOPMENT
OF
ACRYLONITRILE
MANUFACTURE
.
307
11.3.4.
USES
AND
SECONDARY
PRODUCTS
OF
ACRYLONITRILE
.
308
12.
AROMATICS
-
PRODUCTION
AND
CONVERSION
.
311
12.1.
IMPORTANCE
OF
AROMATICS
.
311
12.2.
SOURCES
OF
FEEDSTOCKS
FOR
AROMATICS
.
312
12.2.1.
AROMATICS
FROM
COKING
OF
HARD
COAL
.
313
12.2.2.
AROMATICS
FROM
REFORMATE
AND
PYROLYSIS
GASOLINE
.
314
12.2.2.1.
ISOLATION
OF
AROMATICS
.
317
12.2.2.2.
SPECIAL
SEPARATION
TECHNIQUES
FOR
NON-AROMATIC/AROMATIC
AND
AROMATIC
MIXTURES
.
.
.
318
12.2.3.
POSSIBILITIES
FOR
DEVELOPMENT
OF
AROMATIC
MANUFACTURE
.
323
12.2.4.
CONDENSED
AROMATICS
.
324
12.2.4.1.
NAPHTHALENE
.
325
12.2.4.2.
ANTHRACENE
.
326
XVI
CONTENTS
12.3.
CONVERSION
PROCESSES
FOR
AROMATICS
.
329
12.3.1.
HYDRODEALKYLATION
.
329
12.3.2.
W-XYLENE
ISOMERIZATION
.
330
12.3.3.
DISPROPORTIONATION
AND
TRANSALKYLATION
.
332
13.
BENZENE
DERIVATIVES
.
335
13.1.
ALKYLATION
AND
HYDROGENATION
PRODUCTS
OF
BENZENE
.
335
13.1.1.
ETHYLBENZENE
.
335
13.1.2.
STYRENE
.
339
13.1.3.
CUMENE
.
342
13.1.4.
HIGHER
ALKYLBENZENES
.
343
13.1.5.
CYCLOHEXANE
.
345
13.2.
OXIDATION
AND
SECONDARY
PRODUCTS
OF
BENZENE
.
347
13.2.1.
PHENOL
.
347
13.2.1.1.
MANUFACTURING
PROCESSES
FOR
PHENOL
.
348
13.2.1.2.
POTENTIAL
DEVELOPMENTS
IN
PHENOL
MANUFACTURE
.
355
13.2.1.3.
USES
AND
SECONDARY
PRODUCTS
OF
PHENOL
.
358
13.2.2.
DIHYDROXYBENZENES
.
361
13.2.3.
MALEIC
ANHYDRIDE
.
365
13.2.3.1.
MALEIC
ANHYDRIDE
FROM
OXIDATION
OF
BENZENE
.
366
13.2.3.2.
MALEIC
ANHYDRIDE
FROM
OXIDATION
OF
BUTENE
.
368
13.2.3.3.
MALEIC
ANHYDRIDE
FROM
OXIDATION
OF
BUTANE
.
369
13.2.3.4.
USES
AND
SECONDARY
PRODUCTS
OF
MALEIC
ANHYDRIDE
.
370
13.3.
OTHER
BENZENE
DERIVATIVES
.
373
13.3.1.
NITROBENZENE
.
373
13.3.2.
ANILINE
.
374
13.3.3.
DIISOCYANATES
.
377
14.
OXIDATION
PRODUCTS
OF
XYLENE
AND
NAPHTHALENE
.
385
14.1.
PHTHALIC
ANHYDRIDE
.
385
14.1.1.
OXIDATION
OF
NAPHTHALENE
TO
PHTHALIC
ANHYDRIDE
.
385
14.1.2.
OXIDATION
OF
O-XYLENE
TO
PHTHALIC
ANHYDRIDE
.
387
14.1.3.
ESTERS
OF
PHTHALIC
ACID
AND
DERIVATIVES
.
389
14.2.
TEREPHTHALIC
ACID
.
392
14.2.1.
MANUFACTURE
OF
DIMETHYL
TEREPHTHALATE
AND
TEREPHTHALIC
ACID
.
393
14.2.2.
FIBER
GRADE
TEREPHTHALIC
ACID
.
395
14.2.3.
OTHER
MANUFACTURING
ROUTES
TO
TEREPHTHALIC
ACID
AND
DERIVATIVES
.
397
14.2.4.
USES
OF
TEREPHTHALIC
ACID
AND
DIMETHYL
TEREPHTHALATE
.
400
15.
APPENDIX
.
405
15.1.
PROCESS
AND
PRODUCT
SCHEMES
.
405
15.2.
DEFINITIONS
OF
TERMS
USED
IN
CHARACTERIZING
CHEMICAL
REACTIONS
.
425
CONTENTS
XVII
15.3.
ABBREVIATIONS
FOR
FIRMS
.
427
15.4.
SOURCES
OF
INFORMATION
.
428
15.4.1.
GENERAL
LITERATURE
.
428
15.4.2.
MORE
SPECIFIC
LITERATURE
(PUBLICATIONS,
MONOGRAPHS)
.
429
INDEX
.
439 |
| any_adam_object | 1 |
| author | Weissermel, Klaus 1922-1997 Arpe, Hans-Jürgen |
| author_GND | (DE-588)142804339 (DE-588)105610062 |
| author_facet | Weissermel, Klaus 1922-1997 Arpe, Hans-Jürgen |
| author_role | aut aut |
| author_sort | Weissermel, Klaus 1922-1997 |
| author_variant | k w kw h j a hja |
| building | Verbundindex |
| bvnumber | BV011299555 |
| callnumber-first | T - Technology |
| callnumber-label | TP247 |
| callnumber-raw | TP247 |
| callnumber-search | TP247 |
| callnumber-sort | TP 3247 |
| callnumber-subject | TP - Chemical Technology |
| classification_rvk | VN 5400 VN 5401 |
| ctrlnum | (OCoLC)37332666 (DE-599)BVBBV011299555 |
| dewey-full | 661/.8 |
| dewey-hundreds | 600 - Technology (Applied sciences) |
| dewey-ones | 661 - Technology of industrial chemicals |
| dewey-raw | 661/.8 |
| dewey-search | 661/.8 |
| dewey-sort | 3661 18 |
| dewey-tens | 660 - Chemical engineering |
| discipline | Chemie / Pharmazie |
| edition | 3., completely rev. ed. |
| format | Book |
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| id | DE-604.BV011299555 |
| illustrated | Illustrated |
| indexdate | 2024-08-13T00:24:11Z |
| institution | BVB |
| isbn | 3527288384 |
| language | German English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-007590290 |
| oclc_num | 37332666 |
| open_access_boolean | |
| owner | DE-N32 DE-703 DE-M347 DE-11 |
| owner_facet | DE-N32 DE-703 DE-M347 DE-11 |
| physical | XVII, 464 S. graph. Darst. |
| publishDate | 1997 |
| publishDateSearch | 1997 |
| publishDateSort | 1997 |
| publisher | VCH |
| record_format | marc |
| spelling | Weissermel, Klaus 1922-1997 Verfasser (DE-588)142804339 aut Industrielle organische Chemie Industrial organic chemistry Klaus Weissermel ; Hans-Jürgen Arpe 3., completely rev. ed. Weinheim VCH 1997 XVII, 464 S. graph. Darst. txt rdacontent n rdamedia nc rdacarrier Dt. Ausg. u.d.T.: Weissermel, Klaus: Industrielle organische Chemie Chemistry, organic Tecnologia quimica larpcal Chemistry, Organic Chemistry, Technical Präparative organische Chemie (DE-588)4121505-9 gnd rswk-swf Chemische Synthese (DE-588)4133806-6 gnd rswk-swf Verfahrenstechnik (DE-588)4062781-0 gnd rswk-swf Chemische Industrie (DE-588)4009848-5 gnd rswk-swf Technische organische Chemie (DE-588)4184575-4 gnd rswk-swf Industrie (DE-588)4026779-9 gnd rswk-swf Organische Chemie (DE-588)4043793-0 gnd rswk-swf Technische organische Chemie (DE-588)4184575-4 s DE-604 Chemische Industrie (DE-588)4009848-5 s Chemische Synthese (DE-588)4133806-6 s 1\p DE-604 Organische Chemie (DE-588)4043793-0 s Verfahrenstechnik (DE-588)4062781-0 s 2\p DE-604 Präparative organische Chemie (DE-588)4121505-9 s Industrie (DE-588)4026779-9 s 3\p DE-604 Arpe, Hans-Jürgen Verfasser (DE-588)105610062 aut DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=007590290&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk 2\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk 3\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
| spellingShingle | Weissermel, Klaus 1922-1997 Arpe, Hans-Jürgen Industrial organic chemistry Chemistry, organic Tecnologia quimica larpcal Chemistry, Organic Chemistry, Technical Präparative organische Chemie (DE-588)4121505-9 gnd Chemische Synthese (DE-588)4133806-6 gnd Verfahrenstechnik (DE-588)4062781-0 gnd Chemische Industrie (DE-588)4009848-5 gnd Technische organische Chemie (DE-588)4184575-4 gnd Industrie (DE-588)4026779-9 gnd Organische Chemie (DE-588)4043793-0 gnd |
| subject_GND | (DE-588)4121505-9 (DE-588)4133806-6 (DE-588)4062781-0 (DE-588)4009848-5 (DE-588)4184575-4 (DE-588)4026779-9 (DE-588)4043793-0 |
| title | Industrial organic chemistry |
| title_alt | Industrielle organische Chemie |
| title_auth | Industrial organic chemistry |
| title_exact_search | Industrial organic chemistry |
| title_full | Industrial organic chemistry Klaus Weissermel ; Hans-Jürgen Arpe |
| title_fullStr | Industrial organic chemistry Klaus Weissermel ; Hans-Jürgen Arpe |
| title_full_unstemmed | Industrial organic chemistry Klaus Weissermel ; Hans-Jürgen Arpe |
| title_short | Industrial organic chemistry |
| title_sort | industrial organic chemistry |
| topic | Chemistry, organic Tecnologia quimica larpcal Chemistry, Organic Chemistry, Technical Präparative organische Chemie (DE-588)4121505-9 gnd Chemische Synthese (DE-588)4133806-6 gnd Verfahrenstechnik (DE-588)4062781-0 gnd Chemische Industrie (DE-588)4009848-5 gnd Technische organische Chemie (DE-588)4184575-4 gnd Industrie (DE-588)4026779-9 gnd Organische Chemie (DE-588)4043793-0 gnd |
| topic_facet | Chemistry, organic Tecnologia quimica Chemistry, Organic Chemistry, Technical Präparative organische Chemie Chemische Synthese Verfahrenstechnik Chemische Industrie Technische organische Chemie Industrie Organische Chemie |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=007590290&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT weissermelklaus industrielleorganischechemie AT arpehansjurgen industrielleorganischechemie AT weissermelklaus industrialorganicchemistry AT arpehansjurgen industrialorganicchemistry |