de - Beste verfügbare Techniken (BVT) - Umweltbundesamt
de - Beste verfügbare Techniken (BVT) - Umweltbundesamt
de - Beste verfügbare Techniken (BVT) - Umweltbundesamt
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Verzeichnis <strong>de</strong>r Figures bzw. Abbildungen<br />
Figure 1.1: Sectoral breakdown of EU chemical industry sales (2003) ....................................................... 1<br />
Figure 1.2: Number of enterprises and sales by employment size ............................................................... 2<br />
Figure 1.3: Management of waste streams................................................................................................... 4<br />
Figure 1.4: Major chromophores of commercially important dyes..............................................................5<br />
Figure 1.5: Main uses of organic pigments .................................................................................................. 6<br />
Figure 1.6: Share of the world textile dye market attributable to major manufacturers............................... 7<br />
Figure 1.7: Share of the world organic pigments market attributable to main geographic regions.............. 7<br />
Figure 1.8: Examples of APIs ...................................................................................................................... 8<br />
Figure 1.9: Use of vitamins by sectors....................................................................................................... 10<br />
Figure 1.10: Examples of bioci<strong>de</strong>s and plant health products.................................................................... 11<br />
Figure 1.11: European crop protection market in 2001 showing percentages............................................ 12<br />
Figure 1.12: Western European market (EU and EFTA) by product sector, 2001..................................... 12<br />
Figure 1.13: Real growth in the Western European crop protection market, 1990 – 2001 ........................ 13<br />
Figure 1.14: Examples of some fragrance and flavour substances............................................................. 13<br />
Figure 1.15: Examples of some optical brighteners ................................................................................... 14<br />
Figure 1.16: Examples of some flame-retardants....................................................................................... 15<br />
Figure 1.17: World market for brominated flame-retardant compounds by region ................................... 15<br />
Figure 1.18: Market composition by flame-retardant material................................................................... 16<br />
Figure 1.19: Examples of some plasticisers ............................................................................................... 16<br />
Figure 1.20: Examples of some organic explosives ................................................................................... 17<br />
Figure 2.1: Illustrative example of a synthesis using several unit processes.............................................. 21<br />
Figure 2.2: Typical layout for a multipurpose plant................................................................................... 22<br />
Figure 2.3: Example for the utilisation of the vessels in a production building ......................................... 23<br />
Figure 2.4: Stirred tank reactor (conventional temperature control, left) and loop reactor (right)............. 24<br />
Figure 2.5: Example of an energy supply setup with two boilers .............................................................. 28<br />
Figure 2.6: Typically applied recovery/abatement techniques for exhaust gases on OFC sites................. 30<br />
Figure 2.7: Typically applied recovery/abatement techniques for waste water streams on OFC sites....... 31<br />
Figure 2.8: Typically applied processing units for solvent recovery on OFC sites.................................... 33<br />
Figure 2.9: Examples of aromatic compounds with a bio<strong>de</strong>gradability of more than 80 %....................... 39<br />
Figure 2.10: Examples of aromatic compounds with a bio<strong>de</strong>gradability of less than 80 %....................... 39<br />
Figure 2.11: Typical sequence of operations and related waste streams from N-acetylations ................... 41<br />
Figure 2.12: Diazotisation and azo coupling.............................................................................................. 43<br />
Figure 2.13: Typical sequence of operations for diazotisation and azo coupling....................................... 44<br />
Figure 2.14: Common esterification........................................................................................................... 45<br />
Figure 2.15: Typical sequence of operations for esterification .................................................................. 46<br />
Figure 2.16: Applied abatement techniques for the waste streams from esterification ..............................47<br />
Figure 2.17: Si<strong>de</strong> chain chlorination of toluene <strong>de</strong>rivates .......................................................................... 49<br />
Figure 2.18: Typical sequence of operations for the halogenation to distillable products ......................... 50<br />
Figure 2.19: Typical sequence of operations for halogenation with precipitation of the products.............50<br />
Figure 2.20: Nitration of an aromatic compound ....................................................................................... 51<br />
Figure 2.21: Typical sequence of operations for a nitration....................................................................... 52<br />
Figure 2.22: Typical setup for the manufacture of nitrated alcohols.......................................................... 53<br />
Figure 2.23: Catalytic reduction of aromatic nitro compounds.................................................................. 56<br />
Figure 2.24: Typical sequence of operations for the reduction of an aromatic nitro compound ................ 58<br />
Figure 2.25: Sulphonation of an aromatic system ...................................................................................... 59<br />
Figure 2.26: Typical sequence of operations for a sulphonation................................................................ 60<br />
Figure 2.27: Sulphonation with SO3........................................................................................................... 61<br />
Figure 2.28: Sulphonation with SO3 in liquid phase .................................................................................. 62<br />
Figure 2.29: Sulphonation with SO3 in gas-liquid reaction........................................................................62<br />
Figure 2.30: Sulphochlorination with chlorosulphonic acid....................................................................... 63<br />
Figure 2.31: Typical sequence of operations for sulphochlorination ......................................................... 64<br />
Figure 2.32: Typical sequences of operations for fermentations and downstream work-up ...................... 69<br />
Figure 2.33: Applied abatement techniques for the waste streams from fermentation............................... 71<br />
Figure 3.1: Composition of VOC emissions from the OFC sector in Spain .............................................. 75<br />
Figure 6.1: Comparison of conventional temperature control and constant flux control ......................... 401<br />
OFC_BREF Dezember 2005 xxi