Home
Browse Reports
Search Reports
My Content
My Account
View Cart
Content Map
 
Events
Training



Home > Process Evaluation / Research Planning (PERP) > Bisphenol A > TABLE II.B.2 DOW BISPHENOL A COMMERCIAL EXPERIENCE

Publication Details

TABLE II.B.2 DOW BISPHENOL A COMMERCIAL EXPERIENCE

Generic Keywords: (What are these?)
energy industry, chemical industry, energy market research, market research, market trends, chemical industry developments, chemical research, petrochemical industry, petrochemical research, nexant


Publication Date: 01-SEP-02
Pages: 1
Format: PDF
Price: $100.00
Delivery: Immediate Online Access
   

Description

Table II.B.2 shows the different Dow producers of Bisphenol A, including producer, location, and startup year of each.

down arrow Scroll to this section

This is a section of the Full Report:
Bisphenol A

Publication Date: 01-SEP-02
Format: PDF
Price: $6,000.00
Delivery: Immediate Online Access
   

Description

Bisphenol A (BPA) is prepared by the reaction of one mole of acetone and two moles of phenol to give primarily the para, para´-condensation product, para, para´-isopropylidene-diphenol:

IMAGE: PERPNO16

Strong mineral acids such as hydrochloric or sulfuric can be used as catalysts. Hydrochloric acid is much preferred due to its lower boiling point and relative ease of removal from the reaction mixture. Instead of strong mineral acids, strongly acidic cation exchange resins such as the styrene/divinyl benzene type can be used with or without activity enhancing modifiers. Resin catalysts eliminate catalyst recycle and greatly mitigate equipment corrosion and wastewater treatment problems. To compensate for any activity deficit, reaction temperatures with resin catalysts can be increased to 70-80°C, compared to 50°C with concentrated aqueous or gaseous dry HCl catalyst.

Compounds that contain mercapto (SH) groups or moieties that hydrolyze to mercapto groups are used in catalytic amounts of 1 percent or less of the feed to improve both the formation rate and yield of BPA. Methyl mercaptan is commonly used for this purpose. Other examples of mercaptan promoters are 3-mercaptopropionic acid and 2,2-dimethylthiazoline. The effect of the promoter is attributed to the formation of a more stable carbonium ion, which can exist in higher concentration and thus alkylate the phenol ring faster. Newer ion exchange catalysts are modified to introduce mercapto groups that accomplish the same result while keeping the promoter bound to the resin.

Advantages of the ion exchange catalyzed BPA process are:

  • Much lower investment and maintenance costs due to the use of less costly materials of construction
  • Minimal waste water production, leading to a drastic reduction in the size of the treating system
  • Simpler purification system in that catalyst recovery and recycle are not required

A detailed comparison of process and product parameters for the various processes is discussed in this report. The main factor to note is that resin catalysts have now been improved to the point of essentially the activity and selectivity of the HCI catalyst. Resin catalyzed processes are now also comparable to the HCI catalyzed process in equipment count, and they retain an advantage in less costly construction materials.

Production economics for BPA using resin catalysts and mineral acids are presented. Supply/ demand outlook for BPA on a regional basis is also given.

Purchase Options

To purchase items from this report, click on the checkbox next to each item and click the Purchase button at the bottom of this page.

TABLE OF CONTENTS (PDF document -- No charge)
    SUMMARY
       CHEMISTRY
       PROCESS TECHNOLOGY
       COMPARISON OF ION EXCHANGE AND HCl CATALYZED TECHNOLOGIES
       ECONOMICS OF COMMERCIAL PROCESSES
       COMMERCIAL ANALYSIS
          United States
          Western Europe
          Japan
COMMERCIAL TECHNOLOGY (PDF document -- $1,800.00)
       CHEMISTRY
       ION EXCHANGE CATALYZED PROCESSES
          Dow High-Purity BPA Generation II Process
          Mitsubishi BISA (MCC-BISA) Process
          Sinopec/Lummus Process
       MINERAL ACID CATALYZED PROCESS
       COMPARISON OF ION EXCHANGE AND HCl CATALYZED TECHNOLOGIES
RECENT DEVELOPMENTS (PDF document -- $450.00)
       BACKGROUND
       RESIN CATALYSTS/PROMOTERS
       PROCESSING
       PRODUCT COLOR
       YIELD IMPROVEMENT
ECONOMICS OF COMMERCIAL PROCESSES (PDF document -- $3,600.00)
COMMERCIAL ANALYSIS (PDF document -- $900.00)
       END USES
          Polycarbonate Resins
          Epoxy Resins
          Polyester Resins
          Phenoxy Resins
          Polysulfone Resins
Figure II.B.1 - DOW BISPHENOL A GENERATION II PROCESS (PDF document -- $500.00)
Figure II.B.2 MITSUBISHI MCC- BISA PROCESS (PDF document -- $500.00)
Figure II.B.3 SINOPEC/ LUMMUS BPA PROCESS BLOCK FLOW DIAGRAM (PDF document -- $250.00)
Figure II.C.1 BISPHENOL A VIA HCI CATALYZED PROCESS (PDF document -- $500.00)
Figure II.C.2 BPA BY- PRODUCT HANDLING ARISTECH PATENT (PDF document -- $100.00)
FIGURE IV.1 COST COMPARISON OF BISPHENOL A PROCESSES (PDF document -- $250.00)
FIGURE IV.2 FEED PRICE EFFECT ON BISPHENOL A COST: ION EXCHANGE CATALYZED PROCESS (PDF document -- $100.00)
FIGURE IV.3 INVESTMENT EFFECT ON BISPHENOL A: ION EXCHANGE CATALYZED PROCESS (PDF document -- $100.00)
FIGURE IV.4 CAPACITY EFFECT ON BISPHENOL A COST: ION EXCHANGE CATALYZED PROCESS (PDF document -- $100.00)
FIGURE V.B.1 U.S. BISPHENOL A DEMAND BY APPLICATION, 2001 (PDF document -- $100.00)
FIGURE V.C.1 WEST EUROPEAN BISPHENOL A DEMAND BY APPLICATION, 2001 (PDF document -- $100.00)
FIGURE V.D.1 JAPANESE BISPHENOL A DEMAND BY APPLICATION, 2001 (PDF document -- $100.00)
TABLE II.A.1 LICENSORS OF RESIN CATALYZED BISPHENOL A TECHNOLOGY (PDF document -- $100.00)
TABLE II.B.1 DOW HIGH-PURITY BISPHENOL A TYPICAL PRODUCT QUALITY (PDF document -- $100.00)
TABLE II.B.2 DOW BISPHENOL A COMMERCIAL EXPERIENCE (PDF document -- $100.00)
TABLE II.B.3 MCC-BISA PROCESS FEEDSTOCK MAJOR QUALITY SPECIFICATIONS (PDF document -- $100.00)
TABLE II.B.4 MCC-BISA PRODUCT QUALITY -- POLYCARBONATE GRADE BISPHENOL A (PDF document -- $100.00)
TABLE II.B.5 CT-BISA AND MCC-BISA COMMERCIAL EXPERIENCE (PDF document -- $100.00)
TABLE II.B.6 SINOPEC/LUMMUS PROCESS FEEDSTOCK SPECIFICATIONS (PDF document -- $100.00)
TABLE II.B.7 SINOPEC/LUMMUS BPA PROCESS PRODUCT SPECIFICATIONS (PDF document -- $100.00)
TABLE II.D.1 COMPARISON OF BISPHENOL A PROCESS AND PRODUCT PARAMETERS (PDF document -- $250.00)
TABLE II.D.2 BISPHENOL A SALES SPECIFICATIONS (PDF document -- $100.00)
TABLE II.D.3 PHYSICAL PROPERTIES OF BISPHENOL A (PDF document -- $100.00)
TABLE IV.1 COST OF PRODUCTION ESTIMATE FOR: PHENOL, PROCESS: FROM BENZENE, PROPYLENE (ZEOLITE CAT.) (PDF document -- $1,000.00)
TABLE IV.2 U.S. GULF COAST ECONOMIC SUMMARY FOR BISPHENOL A PROCESSES, FOURTH QUARTER 2001 (PDF document -- $500.00)
TABLE IV.3 COST OF PRODUCTION ESTIMATE FOR: BISPHENOL A PROCESS: FROM PHENOL, ACETONE (ION-EXCH. CAT.) (PDF document -- $1,000.00)
TABLE IV.4 COST OF PRODUCTION ESTIMATE FOR: BISPHENOL A PROCESS: FROM PHENOL, ACETONE (HCI CAT.) (PDF document -- $1,000.00)
TABLE V.B.1 U.S. BISPHENOL A CAPACITY BY PRODUCER, 2001 (PDF document -- $100.00)
TABLE V.B.2 U.S. BISPHENOL A SUPPLY/DEMAND BALANCE (PDF document -- $250.00)
TABLE V.C.1 WEST EUROPEAN BISPHENOL A CAPACITY BY PRODUCER, 2001 (PDF document -- $100.00)
TABLE V.C.2 WEST EUROPEAN BISPHENOL A SUPPLY/DEMAND BALANCE (PDF document -- $250.00)
TABLE V.D.1 JAPANESE BISPHENOL A CAPACITY BY PRODUCER, 2001 (PDF document -- $100.00)
TABLE V.D.2 JAPANESE BISPHENOL A SUPPLY/DEMAND BALANCE (PDF document -- $250.00)

Copyright © 2008, ECNext, Inc. All Rights Reserved