Process for the preparation of precipitated silicas having morphology similar to pyrogenic silicas

BACKGROUND OF THE INVENTION
This invention relates to the production of certain precipitated silicas. In our U.S. Pat. No. 3,954,944 we have described and claimed a new form of precipitated silica which has properties which on a cost/effectiveness basis, are comparable with or better than the very expensive pyrogenic silica produced by methods such as burning silicon tetrachloride. This invention relates to a preferred process for the production of this new silica.
THE PRIOR ART
Pyrogenic silica has, for many years, been used as a rubber filler and as a thixotrope and has commanded a premium price in view of its outstandingly good properties in these and other uses. Workers have, over these many years, attempted to produce, cheaply, silicas having properties comparable, or at least only marginally inferior, to the pyrogenic silica by such expedients as mixing pyrogenic silica with silicas produced by other methods, by the use of a plasma arc to vaporize silica which is then condensed to form fine particles, see, for example, British patent specifications Nos. 1,211,702 and 1,211,703 and by supercritical removal of liquid from pores of silica gels. British specification No. 1,145,510 teaches the fluid energy milling of precipitated silicas to enhance their thixotropic properties but the silicas so produced are demonstrably inferior to those provided by this present invention.
As far back as 1951, Iler in a specification published as U.S. Pat. No. 2,731,326 suggested a two-stage process for the preparation of a precipitated silica useful as a filler for rubber and also as a thickening agent for greases. His silica was also stated to be useful as a carrier for insecticides and as a catalyst.
In the Iler process (U.S. Pat. No. 2,731,326), at Example 11, which is similar to one process of the present invention, primary silica particles are produced by reacting together sodium silicate and sulphuric acid at a temperature of 95.degree. C, the amount of acid being used being equivalent to about 80% of the Na.sub.2 O in the original sodium silicate. The sol obtained is maintained at 95.degree. C and then secondary or "active" silica precipitated. The secondary silica is prepared by adding sodium silicate solution and sulphuric acid to the sol over a period of 2 hours. This secondary silica is then stated to accrete onto the primary silica particles to cement them together so forming the "reinforced silica xerogels," which at Column 8, Iler points out are the products of his invention and are characterized by showing a decrease in specific surface area during their formation which Iler suggests is due to the secondary silica precipitating onto the aggregates and increasing the weight of the aggregates more rapidly than their surface area.
Although, in fact, certain of the process steps in one route to this new silica are similar to the Iler proposals, the process and resultant product do clearly avoid the substantially reinforced aggregates state spelled out in Column 5 of the Iler specification as shown later in Table II.
Field of the Invention
Studies have been made of the structure of pyrogenic silica and it has been concluded that this structure is so different from that of precipitated silicas made hitherto that it is not surprising that the properties, particularly the thixotropic properties are not comparable. Attempts have, therefore, been made to make a precipitated silica which has a morphology more similar to pyrogenic silica and the new precipitated silica which has now been produced has this similar morphology. From experimental work it would appear likely that the new silica provided by the present invention possesses both the appropriate inherent chain-like morphology and the ability to break down to permit the utilization of this morphology. These two characteristics are demonstrated later in terms of performance index of fluid energy milled silica and "breakdown energy" required to reduce the average particle size of the dried silica.
In broad outline, one process for the preparation of this new form of silica comprises preparing primary silica particles by reacting together at a temperature between 85.degree. C and the boiling point, an aqueous solution of sodium silicate and an acid to partially neutralize the silicate solution, adding to the primary precipitated silica an electrolyte to prevent further growth of primary silica and also to flocculate the sol to give an open, chain-like structure which is thought likely to be the foundation of the ultimate pyrogenic silica-like morphology and hence for the thixotropic properties of the final product. After the flocculation stage further silica is produced in the mixture by addition of more acid or more acid and silicate, causing the growth of secondary silica particles to a size limited by the electrolyte concentration and thus producing a product comprising primary silica particle aggregates surrounded by secondary silica particles. These secondary particles presumably serve to isolate the aggregates from each other during the filtration and drying steps and prevent the precipitated silica from losing the ability to form the open structure similar in morphology to that of pyrogenic silica.
The drying step is critical in that it determines the bonding between the silica particles. It is well known that if wet silica particles are dried in contact with each other, the probability of forming strong siloxane bonds is increased and this is undesirable for the production of the silicas of this invention. Hence, if a drying technique is employed in which some material passes more than once through the dryer or the material is otherwise re-wetted and dried then the possibility of additional siloxane bonds being formed is increased and stronger particles so formed. These stronger particles cannot so easily be broken down and thus the open structure is largely lost.
The use of a spray dryer to carry out the drying is particularly advantageous. A spray dryer therefore constitutes a preferred one-pass drying system for achieving drying with minimal aggregation and bonding of particles.
In some applications the technique of incorporating the silica into the final product, be it a plastics film or a synthetic resin or a synthetic rubber will involve a sufficient energy input so that no separate milling step is necessary.
SUMMARY OF THE INVENTION
The present invention provides a process for the production of a precipitated silica having an ignition weight loss of at least 3% between 120.degree. C and 1000.degree. C and a strength such that a sample of the silica having a weight mean particle size on a substantially unimodal distribution in the size range 10-20 microns requires less than 6500 joules of ultrasonic energy as hereinafter defined to reduce the weight mean particle size of the sample to below 3 microns and which silica, after fluid energy milling, has a performance index as hereinafter defined of at least 7.
Accordingly, the present invention provides a process for the preparation of a precipitated silica having an ignition weight loss of at least 3% between 120.degree. C and 1000.degree. C and a strength such that a sample of the silica having a weight mean particle size on a substantially unimodal distribution in the size range 10-20 microns requires less than 6500 joules of ultrasonic energy as hereinafter defined to reduce the weight means particle size of the sample to below 3 microns and which silica, after fluid energy milling, has a performance index as hereinafter defined of at least 7, said process comprising the steps of: reacting an aqueous alkali metal silicate and an acid to form primary silica particles by simultaneously adding to water, under mixing conditions, at a temperature between 85.degree. C and the boiling point of the reaction mixture, the silicate and the acid to a degree of silicate neutralization and a concentration of SiO.sub.2 as indicated in Area A, preferably Area B, in the accompanying drawing; flocculating the primary silica particles produced by the addition of an effective amount of an alkali metal salt flocculant; precipitating secondary silica in the presence of the salt by addition of more acid or more silicate and acid to obtain a final mixture; reducing the pH of the final mixture to below 7, and isolating the silica so produced and subjecting it to purification and single pass drying at a temperature such that the temperature of the silica never exceeds 450.degree. C.
Preferably the alkali metal salt is sodium chloride added as a solution to produce a mixture containing 0.3 to 2 gms NaCl/g of SiO.sub.2 to flocculate the sol.
In a further preferred form of the invention the pH is reduced to 4 or below.
The preferred single pass drying process is spray drying.

DESCRIPTION OF THE DRAWING
The drawing shows key process parameters in the preparation of a precipitated silica in accordance with the present invention.

DETAILED DESCRIPTION OF THE INVENTION
The drawing shows two key process parameters which affect the product; namely the percentage of SiO.sub.2 in the sol and the degree of neutralization of the alkali metal silicate. The numbered points in Areas A and B indicate examples of the invention and the other points indicate examples of the invention and the other points indicate experiments and both sets relate to Table I.
The products of this invention can also be made by feeding the reactants to a tube reactor the conditions of degree of neutralization, SiO.sub.2 content and the like being as previously defined.
The unmilled silica provided by this invention is particularly useful as a reinforcer in silicone rubbers and as an anti-blocking silica for use with plastics films. This silica can also be used after milling to impart thixotropic properties to resinous compositions, paints and the like.
The various parameters employed in defining the silica provided by this invention and in the processes for its manufacture are themselves defined or calculated as follows.
Ignition Weight Loss
Ignition weight loss was measured by pre-drying samples at 120.degree. C to constant weight and then determining the weight loss when the pre-dried samples were heated to 1000.degree. C.
Ultrasonic Energy Strength Test Definition
Particle size distributions in the ultrasonic energy breakdown test were determined with a model T Coulter Counter, supplied by Coulter Electronics Limited, Dunstable, Bedfordshire, England. The silica sample for testing was dispersed at a concentration of 0.5 g/liter at a pH of 3-4 in Isoton which is a 1% saline solution containing 0.1% sodium azide supplied by Coulter Electronics. Ultrasonic energy was then applied to this dispersion using a Soniprobe Type 1130A sold by Dawe Instruments Limited of Western Avenue, Acton, London, England. The instrument used has a cylindrical probe of diameter 0.5 ins. (1.27 cms). The probe was used in 100 ml of the silica dispersion carried in a 150 ml beaker (A) of internal diameter 5.8 cms, the probe extending 3.2 cms under the surface of the dispersion. The amount of ultrasonic energy applied to the dispersion was controlled both by discrete power settings on the ultrasonic generator and by the time over which the power was applied.
The work done on a silica dispersion by application of an amount of ultrasonic energy, was defined in joules calculated from the temperature rise observed when an equal amount of ultrasonic energy was applied to the vessel (A) suitably lagged and containing a volume of water equivalent to that of the silica dispersion used in the test (100 ml). This calibration was carried out over a period during which the time/temperature curve was rectilinear.
Following application of the required amount of work to the dispersion, 1 ml was removed and added to 100 ml of Isoton to provide the final dispersion for analysis with the Coulter Counter.
The Coulter Counter was used with a 140 .mu. tube and particles were counted in each case for a fixed time of 50 secs. The following description of the procedure is given with reference to Table A which contains the basic Coulter Counter data from a breakdown test carried out on Example 8 from Table I. For a given sample of silica, the total oversize volume count (TVC) is first determined for that silica, using a dispersion which has received no ultrasonic work. The TVC is the cumulative oversize volume count over all the particle size ranges covered by the particular Coulter tube being used. In this case the range is 2-50 .mu. and it is essential that the sample used to determine the TVC has all particles within this range. For the purpose of the test, the sample must have a weight mean particle size on a substantially unimodal distribution, with no particles greater than 40 .mu. or less than 3 .mu.. Thus, in Table A the data obtained in determining the TVC for Examples 8 are given in column A, the TVC is equal to 107 and the weight mean particle size which is that size corresponding to one half of the TVC (53.5) is found graphically to be 14.5 .mu..
Table A______________________________________Data from Ultrasonic Breakdown Test on Example 8 Cumulative Oversize Volume Counts Obtained from Coulter CounterChannel Size (.mu.) A B C______________________________________0 50.8 0 0 01 40.3 0 3 12 32.0 1 3 13 25.4 2 3 14 20.2 10 7 25 16.0 38 21 46 12.7 68 41 97 10.08 87 57 158 8.00 98 68 219 6.35 104 74 2710 5.04 106 79 3211 4.00 107 82 3812 3.17 107 84 4313 2.52 107 86 4814 2.00 107 88 53______________________________________ WMPSA - no ultrasonic work 14.5 .mu.B - ultrasonic work done on sample = 550 joules 10.6 .mu.C - ultrasonic work done on sample = 1200 joules 2.0 .mu.
The value of the weight mean particle size (WMPS) for any silica dispersion which has been subjected to ultrasonic work, is defined as that size for which the oversize volume count is equal to one half of the TVC of the control sample, i.e., the sample not subjected to ultrasonic work. Referring to Table A, the TVC for Example 8 is obtained from column A and is equal to 107. The WMPS for samples in column B and C is that size for which the oversize volume count is one half of the TVC from column A, i.e., 53.5. By inspection, it is seen that the WMPS for column B lies between 10.08 .mu. and 12.7 .mu.. However, it is usual to determine the value of WMPS graphically from a plot of cumulative volume count against size. Thus the WMPS for the sample in column B is found to be 10.6 .mu., and for column C it is 2.0 .mu..
It is thus possible to construct a graph of WMPS as a function of the ultrasonic work done on the dispersion, and hence to determine the work necessary to reduce the WMPS of a particular silica sample to 3 .mu..
Weight Mean Particle Size and Particle Size Distribution
Particle size distributions of the fluid energy milled silicas produced were obtained using a Joyce Loebl disc centrifuge obtained from Joyce Loebl & Company Limited, Gateshead, County Durham, England, combined with a suitable analytical method. Samples were prepared for analysis by stirring 2 to 21/2 gms of silica into 50 ml of distilled water and adjusting the pH to 4 with dilute hydrochloric acid. The dispersion was made up to 100 ml with more water and then placed in an ultrasonic bath of the type used as a cleaning bath. Ultrasonic energy was then applied for 30 minutes to effect complete dispersion. Following this the dispersion was stirred continuously to maintain complete dispersion and removed as required. Particle size fractions were obtained from the Joyce Loebl centrifuge using the "Buffered Line Start" technique as described in the instruction manual supplied with the instrument. This technique splits each aliquot of original dispersion into two fractions containing, respectively, particles less than or greater than a size d, where d given by the following equation: ##EQU1## where:
T = centrifuge time in minutes
d = particle size in microns
N = centrifuge speed in rpm
.DELTA..rho. = density difference between sample and spin fluid in g/ml
For the purpose of these measurements the value of 2.21 gms per cc was used in all cases for the density of the silica particles.
.eta. = viscosity of spin fluid in poise
R.sub.1 = starting radius of particles, determined by the volume of spin fluid used in the rotor
R.sub.2 = radius to which a particle of size d settles under the given conditions from a radius R.sub.1.
The silica content of both the original dispersion and of each fraction was determined by dissolving in hydrofluoric acid (5 ml 24% solution) and estimating the silicon content of the resulting solution by atomic absorption spectrometry.
By varying the parameters in equation (X) it is possible to obtain different values for d, and thus by carrying out a set of experiments it is possible to construct a particle size distribution curve for the silica sample.
Performance Index
One valuable use for the silicas provided by this invention is as a thixotropic additive for use in polyester resins, mineral oils and the like. Before determining the performance index each sample of silica was fluid energy milled in a 4 inch (approximately 10.3 cms) air micronizer supplied by Kenry Kingston, Wheathamstead, St. Albans, Hertfordshire, England. The micronizer is of the top feed bottom discharge type and contains 6 jets, each 78 .times. 10.sup.-3 inches (1.98 .times. 10.sup.-1 cm) diameter, arranged to give an impingement circle of 21/2 inches (6.35 cm) diameter. An air relief bag was mounted above the micronizer to retain the fines. The micronizer was operated with a grind pressure of 95 psi (6.65 kg/cm.sup.2) and draws air at a rate of 60-80 scfm (1.7-2.2 Sm.sup.3 /min). The feed rate of silica to the micronizer is 2-3 lbs (0.91-1.35 kg) per hour.
The "fines" fraction from the bag was mixed with the "coarse" fraction before testing.
Experimental work suggests that the rheological performance of which the performance index is an indication can most consistently be measured using a standardized material. A suitable material is a heavy mineral oil obtained from Plough Inc. (United Kingdom) Limited under the trade name NUJOL having the following properties:
specific gravity: 0.880 to 0.900 at 60.degree. F (16.degree. C)
saybolt viscosity: 360/390 at 100.degree. F (38.degree. C)
A silica sample was oven dried at 120.degree. C to constant weight and then combined with NUJOL to give a dispersion of known weight percent silica. The dispersion was passed twice through a triple roll mill with gap setting between the rollers of 0.002 ins. (0.005 mm).
Rheological measurements on the milled sample were made on a Haake Rotoviscometer using the MV II cup and bob assembly thermostatted to 25.degree. C. Measurements were taken after 1 minute at each shear rate starting at the lowest (2.7 sec.sup.-1) and working upwards. Data were plotted out as shear stress against shear rate and the curve was extrapolated to zero shear rate to give the apparent yield stress of the system. For a given silica it was found that the plot of the apparent yield stress (in dyne cm.sup.-2) against the cube of the weight percent silica passes through the origin and is substantially rectilinear. The slope of the line is a measure of the ability of the silica to build a structure in the dispersion and is called hereinafter "the performance index."
The apparent yield stress measurements in polyester resin were carried out to determine the effectiveness of the precipitated silicas in direct comparison with known silicas. The polyester resin was a commercially available resin sold by SRL Limited, Speke, England (formerly Beck Koller Limited) as unfilled Gelcoat 55. The resin was essentially an unsaturated polyester resin solution in styrene containing 33% by weight styrene.
A great deal of work has been carried out to illustrate the differences which exist between the prior art processes and the products and processes of the present invention and to indicate the criticality of the various parameters involved in defining the product and process according to this invention.
For convenience, a general process involving various steps in a preferred process according to this invention will now be described in detail and in the following tables results of work pertinent to defining the invention will be set out, it being understood that the same basic apparatus and processing conditions have been used throughout except where otherwise stated.
A vessel provided with heating equipment and a stirrer was used as the reaction vessel. To this was added a pool of water, heated and maintained at the desired temperature to which was added simultaneously sulphuric acid and sodium silicate solution at addition points above the pool of water and on opposite sides of the pool. The addition of the sulphuric acid and silicate was continued to an appropriate silica concentration and degree of neutralization. Ageing stage 1 was taken here and then the alkali metal salt (generally sodium chloride) was added to flocculate the sol. A second ageing period may be provided after this salt addition. Subsequently, the remaining silicate is neutralized with more acid to a final pH. Optionally a further third ageing period may next be included before the separation by filtration of the precipitated silica from the liquors. Precipitated silica is then spray dried in a spray dryer with an exit temperature of 230.degree. C and milled to the appropriate degree of fineness. The temperature in the drying stage should never exceed 450.degree. C and is preferably never above 350.degree. C.
In Table I there are set out the results obtained from Examples of the invention (Examples 1-15) and Experiments 1-17 indicating results obtained from prior art processes and under conditions similar to, but not within, the scope of the products or processes of this invention.
TABLE I__________________________________________________________________________ Acid Silicate Ageing times Final Added %Pool addition addition (mins) neutralisation electrolyte degree Tempera-volume rate rate for stages: time Final (gNaCl/ % SiO.sub.2 neutrali- tureExample (liters) (ml/min) (ml/min) 1 2 3 (mins) pH gSiO.sub.2) (g/100ml) sation .degree.__________________________________________________________________________ C1 7.2 23(c) 160(a) 10 15 35 25 3.4 1:1 3.0 30 1002 208 342(d) 4210(b) 0 0 32 28 3.8 1:1 3.0 40 1003 201 980(d) 4000(b) 0 O 34 26 3.8 1:1 3.0 50 1004 162 126(d) 5000(b) 0 0 33 27 3.7 1:1 4.25 50 1005 111 126(d) 5000(b) 0 0 27 33 3.5 1:1 5.5 50 1006 97 950(d) 5000(b) 0 0 33 23 2.4 1:1 6.0 55 1007 76 985(c) 4500(a) 10 15 31 29 4.3 1:1 4.9 44 1008 97 900(c) 4500(a) 0 0 30 30 4.3 1:1 4.0 40 1009 140 780(c) 4500(a) 10 15 30 30 3.4 1:1 3.5 35 10010 130 970(d) 5000(b) 0 0 32 28 3.8 1:1 5.0 40 10011 10.8 24(c) 229(a) 0 0 0 30 3.4 0.4:1 3.0 20 10012 7.2 38(c) 200(a) 0 0 0 30 3.4 1:1 3.5 35 9013 7.2 38(c) 200(a) 0 0 0 30 6.0 1:1 3.5 35 10014 14.4 14(c) 143(a) 10 15 30 30 3.4 1:1 1.5 20 10015 14.4 33(c) 179(a) 0 0 0 30 3.4 1:1 2.0 35 100Experiment1 Iler US 2,731,326 Example 11 build up ratio = 1:12 Iler US 2,731,326 Example 11 build up ratio = 2:13 Iler US 2,731,326 Example 144 7.2 38(c) 200(a) 0 0 0 30 3.1 1:1 3.5 35 505 7.2 38(c) 200(a) 0 0 0 30 3.4 1:1 3.5 35 756 7.2 38(c) 200(a) 0 0 0 30 9.0 1:1 3.5 35 1007 10.8 24(c) 273(a) 10 15 30 30 3.4 0 3.0 20 1008 10.8 24(c) 229(a) 0 0 0 30 3.4 1/4:1 3.0 20 1009 7.2 107(c) 356(a) 10 15 35 25 3.0 1:1 4.5 60 10010 7.2 131(c) 375(a) 10 15 35 25 3.4 1:1 4.5 70 10011 4.3 224(c) 494(a) 10 15 35 25 3.4 1:1 5.5 90 10012 75 1030(e) 5000(b) 0 0 33 27 3.8 1:1 7.0 55 10013 43 510(c) 4500(a) 10 15 30 30 4.3 1:1 6.0 25 10014 132 730(d) 4878(b) 0 0 30 30 3.8 1:1 5.0 30 10015 7.2 24(c) 260(a) 10 15 35 25 3.3 1:1 4.2 18 10016 10.8 36(c) 137(a) 0 0 0 30 3.4 1:1 2.0 50 100__________________________________________________________________________17 Iler US 2,731,326 Example 7 build up ratio = 2:1 Weight loss Starting WMPS for Work required to Apparent yield stress 120.degree. C - 1000.degree. C breakdown test break down to Weight % less Performance in polyester resin atExample (%) (microns) 3.mu. (joules) than 0.2.mu. index 41/2% leading (dyne cm.sup.-2)__________________________________________________________________________1 6.1 11.2 1450 49 8.4 3802 5.4 16.6 1700 50 8.53 5.7 18.0 3300 34 9.14 5.0 13.9 4800 -- 8.55 5.8 13.1 4400 39 8.86 5.1 14.1 4500 35 8.47 5.5 12.4 1200 49 7.08 5.5 14.5 1050 34 9.9 4409 4.9 15.2 2000 58 11.2 47510 6.3 16.0 2100 37 7.911 5.2 16.0 1630 39 8.212 5.5 16.2 4000 53 8.313 6.1 17.2 2500 66 9.414 5.7 -- -- 51 8.8 22015 5.0 16.3 6400 46 7.0Experiment1 4.9 -- -- 4 3.4 502 4.1 8.5 1700 8.5 2.7 503 5.2 17.1 >6500 10.4 3.4 204 5.9 16.0 >8000 6 0.6 105 5.1 12.5 >8000 16 5.3 1406 6.2 18.2 >8000 13 1.27 6.4 16.0 >6500 12 1.2 608 5.3 18.2 8000 -- 5.59 5.8 13.5 >10400 27 4.610 4.9 15.0 >6500 16 2.411 5.4 13.1 >6500 24 3.912 5.7 15.0 2500 19 6.713 5.5 -- -- 8 0.4 1014 5.9 12.0 1680 27 5.615 5.1 10.5 6600 20 3.116 5.5 11.5 >8000 18 2.917 5.2 13.0 8000 18 3.0__________________________________________________________________________ (a)sodium silicate specific gravity = 1.10 weight ratio SiO.sub.2 /Na.sub.2 O = 3.3:1 (b)sodium silicate specific gravity = 1.20 weight ratio SiO.sub.2 /Na.sub.2 O = 3.3:1 (c)sulphuric acid specific gravity = 1.06 (d)sulphuric acid specific gravity = 1.12 (e)sulphuric acid specific gravity = 1.18
An indication of the critical nature of the drying step can be obtained from the following experiments. A sample of silica of Example 8 described with reference to Table I was taken and after a normal spray drying step with a gas inlet temperature of 315.degree. C and an exit temperature of 230.degree. C was re-slurried and re-circulated a second, third and fourth time through the spray dryer. The performance index was determined after each passage through the dryer and results obtained were as follows:
______________________________________Times through dryer 1 2 3 4Performance index 9.9 6.8 3.9 3.8______________________________________
Examples 1-15 in Table I indicate processes in Area A of the drawing and Examples 1-13 represent processes in the preferred Area B of the drawing. Examples 9 and 12 and Experiments 4 and 5 indicate the effect of temperature on the process. Examples 9 and 13 and Experiment 6 indicate the effects of the final pH on the product. Example 11 and Experiments 7 and 8 indicate the effect of the sodium chloride flocculant addition. Experiments 9-16 indicate the effect of working outside Area A in the drawing.
Comparisons with the product produced according to the Iler U.S. Pat. No. 2,731,326 are set out in Table II in which data are given in Examples 16, 17 and 18 of the first stage of one process according to this invention and Experiments 1 and 2 also referred to in Table I indicate the results using the Iler process.
The surface area is measured up to completion of neutralization and this causes the time differences in Table II.
TABLE II__________________________________________________________________________ Sili- Elapsed Acid cate Ageing time addi- addi- times Final % Added during tion tion (mins) neutra- % SiO.sub.2 Degree elect- secondary Ratio SurfacePool volume (liters) rate (ml/ min) rate (ml/ min) for stages: 1 2 3 lisation time (min) Final pH (w/v) (g/ 100ml) of neutra- lisation Temp .degree. C rolyte g NaCl/ g silica precipita- tion(min) ##STR1## area (m.sup.2 /g) (a) (b)__________________________________________________________________________Example 7.2 35 200 10 15 30 30 3.0 3.5 35 100 1:1 0 "heel" 28916 10 -- 193 20 -- 228 30 -- 284Example 7.2 19 154 10 15 30 30 2.6 3.0 25 100 1:1 0 "heel" 401 33217 10 -- 235 178 20 -- 267 163 30 -- 288 255Example 7.2 35 200 10 15 80 120 3.0 3.5 35 100 1:1 0 "heel" 349 27218 30 -- 249 189 60 -- 192 161 90 -- 147 143 120 -- 230 212Experi- Iler U.S. Pat. No. 2,731,326 0 "heel" 138ment 2 Example 11 -- build up ratio = 2.0 30 2/3:1 138 final neutralisation time = 90 mins 60 4/3:1 125 90 2:1 113Experi- Iler U.S. Pat. No. 2,731,326 0 "heel" 206ment 1 Example 11 -- build up ratio = 1.0 20 1/3:1 182 final neutralisation time = 60 mins 40 2/3:1 158 60 1:1 139__________________________________________________________________________(1) preparation data sodium silicate specific gravity = 1.10 Examples 16, 17, 18 weight ratio SiO.sub.2 /Na.sub.2 O = 3.3:1 sulphuric acid specific gravity = 1.06(2) surface area data (a) washed with demineralised water followed by water at at pH = 3.0 (b) wash with demineralised
In Tables III and IV data are set out showing the difference between the products according to this invention and those disclosed in the Cabot Corporation British patent specification No. 1,145,510. Table III indicates the viscosity at various shear rates using the silica of Example 8 set out in Table I, compared with the data disclosed by Cabot in BP No. 1,145,510.
TABLE III______________________________________ Viscosity (cps) Example 8Shear rate Dispersed with Dispersed with(sec.sup.-1) Cabot Three Roll Mill High Speed Stirrer______________________________________16.2 985 2900 240032.3 57048.5 415 1150 94097.0 251146 196 520 430291 138437 116 260 220873 881310 78______________________________________ Cabot data 4% silica in paraffin oil [viscosity = 38 cps] silica disperse with high speed stirrer. Example 8 4% silica in mixture of Nujol + dodecane (85:15) [giving a viscosity of 38 cps for the mixture].
Table IV indicates the effect of the Cabot silica compared with the silica of Example 8 in polyster resin compositions.
TABLE IV______________________________________Polyester Resin Data [Brookfield Viscometer]Cabot Data from BP 1,145,5102% micronised silica -- dispersed in Waring Blendor -- resinviscosity -- nominal 300 cps. Viscosity Relative Viscosity6 rpm 1500 cps 5.060 rpm 720 cps 2.4shear thinning index 2.08Example 82% micronised silica -- dispersed with three roll mill -- resinviscosity -- 900 cps. Viscosity Relative Viscosity5 rpm 6080 cps 6.7550 rpm 2450 cps 2.72shear thinning index 2.5______________________________________
From these two tables it will be seen that the silica of Example 8 is significantly more effective than that of the silica disclosed by Cabot.
A sample of the silica produced according to Example 8 was incorporated in a heat curing silicone rubber formulation and comparative data drawn against a fumed silica in a comparable formulation.
Certain of the physical properties of the rubber produced using the silica according to the present invention were not as good as those from the commercially available fumed silica which had a surface area of about 200 m.sup.2 /g but it is thought that these particular features could well be improved by a more thorough washing as would occur on an industrial scale.
TABLE V__________________________________________________________________________ Hardness Tensile Elongation Tear Compression Set Cure .degree. BS psi % psi %__________________________________________________________________________Silica of Example 8 Press Cure only 59 970 280 5.5 51.0 4 hr at 200.degree. C 59 675 210 4.6 23.5 24 hr at 250.degree. C 58 815 190 4.1 17.9Fumed Silica Press Cure only 53 1082 455 4.7 27.9 4 hr at 200.degree. C 55 1110 400 5.8 14.0 24 hr at 250.degree. C 56 983 330 6.6 13.1__________________________________________________________________________ The filler loading in each case was 37 parts filler as received per 100 parts silicone elastomer.

Number	Name	Date
3235331	Nauroth et al.	Feb 1966
3325249	Burke	Jun 1967
3787561	Acker et al.	Jan 1974
3859420	Laufer et al.	Jan 1975
3977893	Wason	Aug 1976

Process for the preparation of precipitated silicas having morphology similar to pyrogenic silicas

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