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8.Pharmaceutical Raw Materials And Pharmaceutical Intermediates
In-depth analysis of the Mechanism of Action
1. Physical adsorption is dominant
- Micropore retention: Micropores with a pore size of less than 2 nm efficiently capture small molecule pigments (such as HMF) and heavy metal ions.
- Specific surface area effect: A surface area of over 1000 m²/g provides a vast number of adsorption sites. For instance, the adsorption capacity of coconut shell carbon for benzene series substances can reach 300 mg/g.
2. Enhanced chemical functionalization
- Surface modification: Silver-loaded carbon inhibits microbial reproduction (Escherichia coli killing rate >99%); Phenolic adsorption enhanced by alkaline carbon (efficiency ↑56.87%);
Targeted design: Iron oxide loaded with carbon is specifically designed for sulfides and is suitable for sulfur-containing active pharmaceutical ingredient workshops.
3. Dynamic optimization
- Diffusion control: Mesopores (2-50 nm) accelerate mass transfer of pollutants and prevent micropore blockage;
- Regeneration cycle: Hot regeneration (800℃) to restore the iodine value to >800, and repeat 5 to 8 times (verified in gold smelting).
Activated carbon in the pharmaceutical field serves as both a "purification guardian" (from raw materials to intermediates) and a "life defense line" (detoxification and blood purification). Its porous structure and surface engineering will continue to empower drug safety and green manufacturing.
The mechanism and application of activated carbon in the pharmaceutical industry |
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Application link |
Core role |
Mode of action |
Activated carbon type |
Key process parameters/cases |
Technical feature |
Refining of active pharmaceutical ingredients |
Decolorization and impurity removal |
Physical adsorption (micropores retain pigment macromolecules, specific surface area 300-1500 m²/g) |
PAC |
Addition amount: 0.1%-1.5%, pH: 3-7, temperature: 40-70℃; The decolorization rate of xylitol is over 97% |
Avoid excessive adsorption to prevent the loss of active ingredients
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Purification of pharmaceutical intermediates |
Purification of solvents/reaction media |
Selectively adsorb metal ions (such As Pb²⁺, As³⁺) and organic by-products |
GAC |
ppmDynamic flow velocity: 1-2 BV/h The heavy metal residue in the circulating solvent is less than 0.1 ppm |
Extend the service life of the solvent and reduce production costs |
Pharmaceutical environmental control |
VOCs and Waste Gas treatment |
Physical adsorption (van der Waals forces) is the main method, supplemented by chemical adsorption (functional groups on the surface of modified carbon) |
Box-type carbon tower |
The TVOC removal rate is over 95%, and the pressure drop is less than 150 Pa. The TVOC of pharmaceutical enterprises in Shandong has decreased from 1.2 mg/m³ to 0.45 mg/m³ |
Modular design, suitable for GMP cleanliness requirements |
Medicinal activated carbon |
Oral antidote |
Adsorb gastrointestinal toxins (molecular weight 150-500 Da) and block blood absorption |
Medical-grade powdered carbon |
Dose: 1 g/kg body weight; Administer the drug within 30 minutes for poisoning first aid, and the poison clearance rate is 50-60% |
It should be avoided to be used in combination with anticoagulants and antiviral drugs |
Hemoperfusion purification |
Directly adsorb uremic toxins and drug residues (such as excessive antibiotics) in the blood |
Coated carbon particles |
The blood flow rate is 200 mL/min; The creatinine clearance rate of patients with uremia increased by 40% |
The biocompatible coating prevents the leakage of carbon particles |
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Effluent treatment |
Removal of refractory organic substances |
Ozone combined catalysis (·OH radical oxidation) + activated carbon adsorption synergistic effect |
O₃/GAC combined process |
When the flow rate of O₂ is 120 L/h + GAC 30 g, the COD removal rate is 92% |
Break through the limitations of traditional adsorption capacity |