A carbon disulfide conversion-absorption type desulfurizer and its preparation method
A technology of carbon disulfide and desulfurization agent, which is applied in the field of desulfurization, can solve the problems of inapplicable treatment, etc., and achieve the effect of wide range of concentration adaptation and good conversion-absorption
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0036] Preparation of metatitanic acid:
[0037] In the reactor, weigh 5kg of solid ferrous sulfate, a by-product of titanium dioxide production by sulfuric acid method, add 6L of water to dissolve, heat at 60°C for 30min, add acid to adjust the pH value to 1, add flocculant polyacrylamide and filter while hot to obtain partial Titanic acid solid A, the metatitanic acid A was dried at 110° C. for 1 h.
[0038] In the reactor, weigh 1.67 kg of solid ferrous sulfate, a by-product of titanium dioxide production by sulfuric acid method, add 6 L of water to dissolve, heat at 100° C. for 30 min, add acid to adjust the pH value to 2, add flocculant polyacrylamide, and filter while hot to obtain Metatitanic acid solid B, the metatitanic acid B was dried at 110° C. for 1 h.
Embodiment 2
[0040] Anatase TiO 2 , K 2 O and γ-Al 2 O 3 Preparation of:
[0041] The metatitanic acid A, K prepared in step (1) 2 CO 3 and pseudo-boehmite were calcined at 500 °C to prepare anatase TiO 2 , K 2 O and γ-Al 2 O 3 .
Embodiment 3
[0043] The desulfurizer described in this example contains the following components: magnetic iron oxide red Fe 21.333 O 32 , 50 parts by weight; anatase TiO 2 , 5 parts by weight; K 2 O, 2 parts by weight; γ-Al 2 O 3 , 5 parts by weight; bentonite, 5 parts by weight.
[0044] The preparation method of the desulfurizer of catalytic conversion-absorption type carbon disulfide described in the present embodiment is:
[0045] (1) Weigh solid FeSO in a beaker 4 ·7H 2 O500g, add 454ml water, dissolve in a 40°C water bath, after complete dissolution, add Na 2 CO 3 190g, the alkali ratio of the two is 1; stir for 2h to carry out the precipitation reaction, filter after the precipitation is completed, and calcine the filter cake at 350 ° C for 3h to obtain magnetic iron oxide red Fe 21.333 O 32 . The prepared magnetic iron oxide red Fe 21.333 O 32 XRD pattern of figure 1 shown.
[0046] (2) 50 parts by weight of the magnetic iron oxide red Fe 21.333 O 32 , 5 parts by ...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 

