Production of precipitated silica employing a fast blender

Abstract

A unique method for preparing precipitated silica entails reacting a silicate with an acidifying agent to obtain a suspension of precipitated silica, and separating and drying the suspension, and further wherein the precipitation includes contacting a silicate with an acidifying agent in an acidic medium in a fast blender.

1 - 33 . (canceled) 
     
     
         34 . A method for preparing precipitated silica comprising reacting a silicate with an acidifying agent to obtain a suspension of precipitated silica, and separating and drying this suspension, and further wherein the precipitation comprises contacting a silicate with an acidifying agent in an acidic medium in a fast blender. 
     
     
         35 . A method for preparing precipitated silica comprising reacting a silicate with an acidifying agent to obtain a suspension of precipitated silica, and separating and drying this suspension, and further wherein the precipitation comprises contacting a silicate with an acidifying agent in an acidic medium in a zone of turbulent flow. 
     
     
         36 . The method as defined by  claim 34 , wherein the contacting of a silicate with an acidifying agent is carried out at a pH ranging from 2 to 5.5. 
     
     
         37 . The method as defined by  claim 34 , wherein the contacting of a silicate with an acidifying agent is carried out in continuous mode. 
     
     
         38 . The method as defined by  claim 34 , wherein the reaction medium resulting from said contacting of a silicate with an acidifying agent is introduced into at least one optionally stirred reactor. 
     
     
         39 . The method as defined by  claim 38 , wherein said at least one reactor operates in semi-continuous mode. 
     
     
         40 . The method as defined by  claim 34 , wherein the contacting of a silicate with an acidifying agent is carried out in a fast blender selected from among symmetrical T or Y blenders (or tubes), asymmetrical T or Y blenders or tubes, tangential jet blenders, Hartridge-Roughton blenders, vortex blenders, and rotor-stator blenders. 
     
     
         41 . The method as defined by  claim 34 , wherein the contacting of a silicate with an acidifying agent is carried in a tangential jet blender, Hartridge-Roughton or vortex blender which comprises a chamber having at least two tangential inlets via which the silicate and acidifying agent are separately introduced, and an axial outlet via which the reaction medium exits. 
     
     
         42 . The method as defined by  claim 41 , wherein said at least two tangential inlets are located symmetrically, and in opposition, about the centerline of said chamber. 
     
     
         43 . The method as defined by  claim 34 , comprising conducting the precipitation as follows:
 (i) simultaneously adding silicate and acidifying agent to said fast blender, the pH of the reaction medium (pH 1 ) ranging from 2 to 5.5,   (ii) introducing the reaction medium issuing from step (i) into at least one stirred reactor, the pH of the reaction medium (pH 2 ) in the reactor being regulated from 2 to 5.5, optionally with pH 2 ≧pH 1 ,   (iii) adding silicate to the reaction medium, in the stirred reactor, until the pH value of the reaction mixture ranges from 7 to 10,   (iv) simultaneously adding silicate and acidifying agent to the reaction medium, in the stirred reactor, and maintaining the pH of the reaction medium from 7 to 10,   (v) interrupting the silicate addition while continuing to add acidifying agent to the reaction medium of the stirred reactor until the pH value of the reaction medium in the stirred reactor is less than 6.   
     
     
         44 . The method as defined by  claim 43 , wherein, in step (ii), to regulate the pH of the reaction medium (pH 2 ) in the reactor from 2 to 5.5, acidifying agent or, optionally, silicate or a basifying agent, is added simultaneously to the reaction mixture issuing from step (i). 
     
     
         45 . The method as defined by  claim 43 , wherein the pH 1  and pH 2  range from 2.5 to 5. 
     
     
         46 . The method as defined by  claim 43 , wherein pH 2 ≧pH 1 . 
     
     
         47 . The method as defined by  claim 43 , wherein the entire precipitation is carried out at a temperature ranging from 70° to 95° C. 
     
     
         48 . The method as defined by  claim 43 , wherein the temperature of the reaction medium ranges from 70° to 86° C. during steps (i) and (ii). 
     
     
         49 . The method as defined by  claim 43 , wherein the temperature of the reaction medium is increased, during step (iii), to a value of from 85° to 95° C., and then maintained at this value during steps (iv) and (v). 
     
     
         50 . The method as defined by  claim 43 , wherein said fast blender is a tangential jet blender, Hartridge-Roughton or vortex blender, comprising a chamber having at least two tangential inlets via which the silicate and acidifying agent are separately introduced, and an axial outlet via which the reaction medium exits, the at least two tangential inlets optionally being located symmetrically about the centerline of said chamber. 
     
     
         51 . The method as defined by  claim 34 , wherein the residence time through the fast blender is shorter than 1 second. 
     
     
         52 . The method as defined by  claim 34 , wherein the drying is carried out by spray drying. 
     
     
         53 . The method as defined by  claim 34 , wherein the separation comprises a filtration carried out employing a filter press. 
     
     
         54 . The method as defined by  claim 34 , wherein the separation comprises a filtration carried out employing a nozzle spray dryer. 
     
     
         55 . The method as defined by  claim 34 , wherein the separation comprises a filtration carried out employing a vacuum filter. 
     
     
         56 . The method as defined by  claim 34 , wherein the separation comprises a filtration carried out employing a turbine spray dryer. 
     
     
         57 . The method as defined by  claim 43 , wherein the precipitated silica product has:
 a CTAB specific surface area (S CTAB ) of from 40 to 525 m 2 /g,   a BET specific surface area (S BET ) of from 45 to 550 m 2 /g,   a width Ld ((d84−d16)/d50) of object size distribution measured by XDC grain-size analysis after ultrasonic disaggregation of at least 0.91, and   a pore volume distribution such that the ratio V (d5-d50) /V (d5-d100)  is at least 0.66.   
     
     
         58 . The method as defined by  claim 43 , wherein the precipitated silica product has:
 a CTAB specific surface area (S CTAB ) of from 40 to 525 m 2 /g,   a BET specific surface area (S BET ) of from 45 and 550 m 2 /g, and   a pore distribution width 1 dp higher than 0.70.   
     
     
         59 . The method as defined by  claim 43 , wherein the precipitated silica product has:
 a CTAB specific surface area (S CTAB ) of from 40 and 525 m 2 /g,   a BET specific surface area (S BET ) of from 45 and 550 m 2 /g,   a width L′d ((d84−d16)/d50) of object size distribution lower than 500 nm, measured by XDC grain size analysis after ultrasonic disaggregation of at least 0.95, and   a pore volume distribution such that the ratio V (d5-d50) /V (d5-d100)  is at least 0.71.   
     
     
         60 . The method as defined by  claim 43 , wherein the precipitated silica product has:
 a CTAB specific surface area (S CTAB ) of from 40 to 525 m 2 /g,   a BET specific surface area (S BET ) of from 45 to 550 m 2 /g,   a width L′d ((d84−d16)/d50) of object size distribution lower than 500 nm, measured by XDC grain size analysis after ultrasonic disaggregation of at least 0.90, and   a pore volume distribution such that the ratio V (ds-d50) /V (d5-d100)  is at least 0.71.   
     
     
         61 . The method as defined by  claim 43 , wherein the precipitated silica product has an object size such that the grain size mode measured by XDC grain-size analysis after ultrasonic disaggregation meets the following condition:
 Mode XDC (nm)≧(5320/S CTAB  (m 2 /g))+8.   
     
     
         62 . The method as defined by  claim 43 , wherein the precipitated silica product has:
 a CTAB specific surface area (S CTAB ) of from 60 to 330 m 2 /g, and   a BET specific surface area (S BET ) of from 70 to 350 m 2 /g.   
     
     
         63 . The method as defined by  claim 43 , wherein the precipitated silica product has a CTAB specific surface area (S CTAB ) of from 90 to 230 m 2 /g and a BET specific surface area (S BET ) of from 110 to 270 m 2 /g. 
     
     
         64 . The method as defined by  claim 43 , wherein the precipitate obtained comprises substantially spherical beads having an average particle size of at least 80 μm. 
     
     
         65 . The method as defined by  claim 43 , wherein the precipitate obtained comprises a powder having an average particle size of at least 15 μm. 
     
     
         66 . The method as defined by  claim 43 , wherein the precipitate obtained comprises granules having a particle size of at least 1 mm. 
     
     
         67 . The method as defined by  claim 35 , wherein the residence time in the zone of turbulent flow is shorter than 1 second.