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sspl@shivsilica.com
ISO
Quality
Pharma Application
Pharmaceutical
| Sr No: | Descripation of Test | Specification / Limit | FIL-P |
|---|---|---|---|
| 1 | Appearance | White Fine light amorphous odourless powder | White Fine light amorphous odourless powder |
| 2 | Packing | kgs | 10 |
| 3 | pH (5 % w/v) Aq. Sus. | - | 3.5 to 5.0 |
| 4 | BET Surface area | m2/gm | 170-180 |
| 5 | Moisture Content ( at 105℃ for 2 hr ) | % ( Max ) | 1.5 |
| 6 | Bulk Density,Tapped Method | gms/lit | 60-130 |
| 7 | Loss on Ignition ( at 1000℃ for 2 hrs. on anhydrous basis) | % ( Max) | 5.00 |
| 8 | Si2 on Anhydrous Basis | % ( Min ) | 99 |
| 9 | Chloride | ppm | Not more than 250 |
| 10 | Total Heavy Metal ( as Pb ) | ppm | Not more than 250 |
| 11 | Behaviour with water | Hydrophilic | Hydrophilic |
Packing: HDPE Laminated Bags with inside Polyliner
Also available: Product confirming to the buyer’s specifications against bulk requirement
