Modelling and optimisation of an industrial batch process
- Classification:Chemical Auxiliary Agent
- CAS No.:117-84-0
- Other Names:Liquid DOP, DOP oil
- MF:C24H38O4, C24H38O4
- EINECS No.:201-557-4
- Purity:99.5%min, 99.5%min
- Type:pvc additive
- Usage:Plastic Auxiliary Agents, Plasticizer
- MOQ::10 Tons
- Package:25kg/drum
- Advantage:Stable
- Payment:T/T
Dioctyl phthalate (DOP) is used in substantial quantities in industry, primarily as a plasticiser for PVC and other polymers. One route to its production is via the esterification of 2
In a typical experiment, the desired amounts of DOP and catalyst werecharged into the reactor. The reactor was sealed and purged 2–3 times with pressurized H 2 gas to remove the air. The
Evaluasi Energi Pada Reaktor Kontinyu Terhadap
- Classification:Chemical Auxiliary Agent
- CAS No.:117-84-0
- Other Names:DOP Bis(2-ethylhexyl) phthalate
- MF:C6H4(COOC8H17)2
- EINECS No.:201-557-4
- Purity:99.5%min
- Type:Adsorbent, Carbon Black
- Usage:Coating Auxiliary Agents, Leather Auxiliary Agents, Plastic Auxiliary Agents, Rubber Auxiliary Agents
- MOQ:200kgs
- Package:200kgs/battle
- Shape:Powder
- Payment:T/T
- Application:PVC Plasticizer
ABSTRAK: Dioctyl Phthalate (DOP) merupakan bahan pembantu di beberapa industri bahan-bahan plastik yang biasanya disebut plasticizer seperti pada jacket needs to be added to
For example, in microwave-assisted reactive distillation to produce dioctyl phthalate, the MIRVC effect accelerated the removal of the strong MW-absorbing component water in the reaction
Hydrogenation of dioctyl phthalate over supported Ni catalysts
- Classification:Chemical Auxiliary Agent
- CAS No.:117-84-0
- Other Names:DOP Bis(2-ethylhexyl) phthalate
- MF:C24H38O4, C24H38O4
- EINECS No.:201-557-4
- Purity:99.0%Min
- Type:Adsorbent
- Usage:Leather Auxiliary Agents, Plastic Auxiliary Agents, Rubber Auxiliary Agents
- MOQ::10 Tons
- Package:25kg/drum
- Application:PVC Plasticizer
The conversion of DOP decreased with the increase of WHSV of DOP. At the WHSV of 46 h −1, the conversion of DOP dropped to about 72, 55 and 34% on the Ni/Al 2 O 3
The synthesis of dioctyl phthalate (DOP) involves mono-(2-ethylhexyl) phthalate (MEHP) formation firstly by phthalic anhydride (PA) with 2-ethyl hexanol (2-EH) and further
Biochemical pathways and enhanced degradation of di-n
- Classification:Chemical Auxiliary Agent, Chemical Auxiliary Agent
- cas no 117-84-0
- Other Names:Dioctyl Phthalate DOP
- MF:C6H4(COOC8H17)2
- EINECS No.:201-557-4
- Purity:99.5%min
- Type:Chemical additives, Chemical dop plasticizer 99%
- Usage:Coating Auxiliary Agents, Leather Auxiliary Agents, Petroleum Additives, Plastic Auxiliary Agents, Rubber Auxiliary Agents, Surfactants, Textile Auxiliary Agents
- MOQ:200kgs
- Package:200kgs/battle
- Application:PVC Plasticizer
- Item:T/T,L/C
Di-n-octyl phthalate (DOP), belonging to the family of phthalic acid esters (PAEs), is one of the most commonly utilized plasticizers and widely used as Biochemical pathways and
DOP (Dioctyl Phthalate) is a commonly used plasticizer. It belongs to the class of phthalate esters, which are substances added to plastics to increase their flexibility, durability and workability. We are professional
DOP Reactors: The Heart of Plasticizer Production
- Classification:Chemical Auxiliary Agent, Chemical Auxiliary Agent
- cas no 117-84-0
- Other Names:Dop
- MF:C24H38O4, C24H38O4
- EINECS No.:201-557-4
- Purity:99.5%min, 99.5%min
- Type:Plasticizer
- Usage:Leather Auxiliary Agents, Plastic Auxiliary Agents, Plasticizer
- MOQ::10 Tons
- Package:25kg/drum
- Shape:Powder
- Application:PVC Plasticizer
DOP reactors are large-scale chemical processing vessels designed specifically for the production of dioctyl phthalate. These reactors are typically made of stainless steel or other corrosion
48 Advanced synthesis of dioctyl phthalate (DOP) and dibutyl phthalate (DBP) plasticizers Full Paper CTAIJ, 4(2) December 2009 An Indian Journal chemical technology The ester productivity and quality depend essentially on the applied catalyst and reaction conditions. Up to now, the synthesis processes of carboxylic ester in in-