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10193-36-9 Usage

Hazard

A poison.

Check Digit Verification of cas no

The CAS Registry Mumber 10193-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,9 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10193-36:
(7*1)+(6*0)+(5*1)+(4*9)+(3*3)+(2*3)+(1*6)=69
69 % 10 = 9
So 10193-36-9 is a valid CAS Registry Number.
InChI:InChI=1/4H2O.Si/h4*1H2;/q;;;;+4/p-4

10193-36-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name silicic acid

1.2 Other means of identification

Product number -
Other names SILICIC ACID (H4O4SI)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10193-36-9 SDS

10193-36-9Synthetic route

silicic acid tetrabenzyl ester
4424-00-4

silicic acid tetrabenzyl ester

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With palladium-platinum; hydrogen; aniline In N,N-dimethyl acetamide at 20℃; for 2h; Concentration; Solvent;96%
silicic acid tetrabenzyl ester
4424-00-4

silicic acid tetrabenzyl ester

A

pyrosilicic acid
20638-18-0

pyrosilicic acid

B

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With palladium-platinum; hydrogen; aniline at 20℃; for 2h; Concentration; Reagent/catalyst; Time;A 6%
B 92%
With palladium-platinum; hydrogen In N,N-dimethyl acetamide at 20℃; for 2h;A 34%
B 13%
sodium silicate octahydrate

sodium silicate octahydrate

A

pyrosilicic acid
20638-18-0

pyrosilicic acid

B

cyclo trisiloxanehexaol
20638-19-1

cyclo trisiloxanehexaol

C

(HO)3SiOSi(OH)2OSi(OH)3
57956-13-5

(HO)3SiOSi(OH)2OSi(OH)3

D

(HO)2SiOSi(OH)2OSi(OH)2O(Si(OH)2O)
20761-28-8

(HO)2SiOSi(OH)2OSi(OH)2O(Si(OH)2O)

E

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With sulfuric acid Kinetics; byproducts: H10Si6O17, H10Si8O21, polysilicate; Na2H2SiO4*8H2O added to zeolite ion-exchange/H2SO4 at 2°C; filtered, product yield dependence to ageing time at room temp.;A 14%
B n/a
C n/a
D 5%
E 51%
silicic acid tetrabenzyl ester
4424-00-4

silicic acid tetrabenzyl ester

A

pyrosilicic acid
20638-18-0

pyrosilicic acid

B

cyclo trisiloxanehexaol
20638-19-1

cyclo trisiloxanehexaol

C

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With palladium-platinum; hydrogen at 20℃; for 2h;A 36%
B 47%
C 8%
sodium silicate

sodium silicate

A

pyrosilicic acid
20638-18-0

pyrosilicic acid

B

cyclo trisiloxanehexaol
20638-19-1

cyclo trisiloxanehexaol

C

(HO)3SiOSi(OH)2OSi(OH)3
57956-13-5

(HO)3SiOSi(OH)2OSi(OH)3

D

(HO)2SiOSi(OH)2OSi(OH)2O(Si(OH)2O)
20761-28-8

(HO)2SiOSi(OH)2OSi(OH)2O(Si(OH)2O)

E

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With sulfuric acid Kinetics; byproducts: H10Si6O17, H10Si8O21, polysilicate; Na2SiO3 added to zeolite ion-exchange/H2SO4 at 2°C; filtered, product yield dependence to ageing time at room temp.;A 8%
B n/a
C n/a
D 4%
E 28%
ammonia

ammonia

silica gel

silica gel

tin(IV) chloride
7646-78-8

tin(IV) chloride

A

tin hydroxide

tin hydroxide

B

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In water pH=5 - 7;
tetramethylorthosilicate
681-84-5

tetramethylorthosilicate

silicic Acid
10193-36-9

silicic Acid

water
7732-18-5

water

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In neat (no solvent) Kinetics; solid SiO2 reacted with H2O vapor;
sulfuric acid
7664-93-9

sulfuric acid

silicon
7440-21-3

silicon

A

silicic Acid
10193-36-9

silicic Acid

B

sulfur
7704-34-9

sulfur

monosilane
7440-21-3

monosilane

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

mercury(I) chloride

mercury(I) chloride

C

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With water; mercury dichloride In water
tetraethoxy orthosilicate
78-10-4

tetraethoxy orthosilicate

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In hydrogenchloride saponification of distd. Si(OC2H5)4 in n/500-HCl-soln.;;
In water by a hydrolytic process;;
In hydrogenchloride saponification of distd. Si(OC2H5)4 in n/500-HCl-soln.;;
sodium metasilicate nonahydrate

sodium metasilicate nonahydrate

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In water salt dissolved in a minimum amount of water added under vigorous stirring to an acidic medium with excess H(1+); not isolated;;
magnesium hexafluorosilicate
16949-65-8

magnesium hexafluorosilicate

sodium hydroxide
1310-73-2

sodium hydroxide

A

magnesium fluoride

magnesium fluoride

B

silicic Acid
10193-36-9

silicic Acid

C

sodium fluoride

sodium fluoride

Conditions
ConditionsYield
In water boiling MgSiF6 with NaOH;;
silica

silica

water
7732-18-5

water

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In water Kinetics; investigation of the kinetics of quartz dissoln. at 25°C: pH range 4.5-10.5, 25°C, ionic strength 0.010 mol/l; concn. of dissolved silicon was measured by react. with NH4-molybdate and reduction to form silicomolybdenum compounds; determination of silicon concn. from the absorbance of soln. at 810 nm;
silica

silica

water
7732-18-5

water

A

silicic acid

silicic acid

B

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In gaseous matrix react. of H2O/O2-stream with quartz frit at 1300°C; not isolated, MS;
water
7732-18-5

water

sodium hydroxide
1310-73-2

sodium hydroxide

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In water the soln. of sodium silicate passed through the cation-exchanger;
water
7732-18-5

water

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

A

fluorosilicic acid

fluorosilicic acid

B

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In water introduction of SiF4 into H2O;; not isolated (in soln.);;
In water introduction of SiF4 into H2O;; not isolated (in soln.);;
water
7732-18-5

water

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

A

hydrogen fluoride
7664-39-3

hydrogen fluoride

B

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In neat (no solvent)
tetrachlorosilane
10026-04-7, 53609-55-5

tetrachlorosilane

water
7732-18-5

water

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In water byproducts: HCl; dry N2 and vapor of SiCl4 is slowly passed into water in presence of Ag2O under vigorous stirring at 0°C;;
In water
disilicon hexafluoride
13830-68-7

disilicon hexafluoride

water
7732-18-5

water

A

fluorosilicic acid

fluorosilicic acid

B

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In water hydrolysis;;
tetraethoxy orthosilicate
78-10-4

tetraethoxy orthosilicate

water
7732-18-5

water

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In ethanol; water by diln. in deionised water of tetraethyl orthosilicate dissolved in ethanol;
In ethanol; water byproducts: C2H5OH; reaction of hydrolysis;
With hydrogenchloride for 0.5h;
potassium chloride

potassium chloride

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

A

potassium hexafluorosilicate

potassium hexafluorosilicate

B

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With water In ethanol; water byproducts: HCl;
trifluorosilane
13465-71-9

trifluorosilane

A

fluorosilicic acid

fluorosilicic acid

B

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With water In water byproducts: H2;
With sodium hydroxide In sodium hydroxide byproducts: H2; decompn. with formation of vapor;;
With NaOH In sodium hydroxide byproducts: H2; aq. NaOH; decompn. with formation of vapor;;
With H2O In water byproducts: H2;
sodium hexafluorosilicate

sodium hexafluorosilicate

sodium hydroxide
1310-73-2

sodium hydroxide

A

silicic Acid
10193-36-9

silicic Acid

B

sodium fluoride

sodium fluoride

Conditions
ConditionsYield
In not given decompn. with NaOH-soln.;;
In not given decompn. with NaOH-soln.;;
chlorotriethoxysilane
4667-99-6

chlorotriethoxysilane

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With H2O
trichlorosilane
10025-78-2

trichlorosilane

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

mercury(I) chloride

mercury(I) chloride

C

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With water; mercury dichloride In water HSiCl3 dissolved in dry dibutylether;;
sodium orthosilicate

sodium orthosilicate

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With cation exchange resin diluted after cation exchange;
lithium silicate

lithium silicate

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In sulfuric acid solution of fine powdered Li orthosilicate in aq. H2SO4 and treatment by liquid NH3 at -17 °C;; pptn. in the solution;;
disilicon hexafluoride
13830-68-7

disilicon hexafluoride

A

fluorosilicic acid

fluorosilicic acid

B

1.2-dioxo-disilanediol
181778-33-6

1.2-dioxo-disilanediol

C

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With H2O In water byproducts: H2; reaction by hydrolysis in moist air;;
tetraisocyanatosilane
3410-77-3

tetraisocyanatosilane

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With H2O In water byproducts: HNCO; decompn. by hydrolysis;;
With H2O In water byproducts: HNCO; decompn. by hydrolysis;;
tin hydroxide

tin hydroxide

silicic Acid
10193-36-9

silicic Acid

Reaxys ID: 11346541

Reaxys ID: 11346541

Conditions
ConditionsYield
With ammonium molybdate; nitric acid In water at 650℃; for 1h; pH=2 - 4;
silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
In neat (no solvent) calcination at 773 K for 5 h;
poly(L-lysine) Conversion of starting material;
In neat (no solvent) H4SiO4 heated at 300°C in vacuum;
pyrosilicic acid
20638-18-0

pyrosilicic acid

silicic Acid
10193-36-9

silicic Acid

Conditions
ConditionsYield
With aq. Na3PO4 or aq. NaOAc; polyamine In water Kinetics; aq. solns. of Na3PO4, polyamine, mono/disilicic acid mixed at 25°C; aliquots removed and centrifuged; precipitated SiO2 dissolved in NaOH (5min at 90°C), quantified by molybdate method;
sodium aluminate

sodium aluminate

silicic Acid
10193-36-9

silicic Acid

aluminum trihydroxide

aluminum trihydroxide

Conditions
ConditionsYield
In not given stirring with freshly pptd. H2SiO3;
In not given stirring with freshly pptd. H2SiO3;
silicic Acid
10193-36-9

silicic Acid

calcium carbonate

calcium carbonate

larnite

larnite

Conditions
ConditionsYield
In neat (no solvent) mixing, grinding, pressing, heating (1300°C);
silicic Acid
10193-36-9

silicic Acid

calcium carbonate

calcium carbonate

calcium metasilicate

calcium metasilicate

Conditions
ConditionsYield
In neat (no solvent) mixing, grinding, pressing, heating (1300°C);
silicic Acid
10193-36-9

silicic Acid

calcium carbonate

calcium carbonate

alite

alite

Conditions
ConditionsYield
In neat (no solvent) mixing, grinding, pressing, heating (1300°C);
silicic Acid
10193-36-9

silicic Acid

lithium fluoride

lithium fluoride

A

Si(OH)3F
39630-75-6

Si(OH)3F

B

SiF6(2-)*H(1+)=HSiF6(1-)
56977-47-0

SiF6(2-)*H(1+)=HSiF6(1-)

C

Si(OH)2F(1+)
201295-48-9

Si(OH)2F(1+)

D

silicon tetrafluoride
7783-61-1

silicon tetrafluoride

E

hexafluorosilicate anion
17084-08-1

hexafluorosilicate anion

Conditions
ConditionsYield
With water; lithium perchlorate In water 25°C, 3 m LiClO4 medium, fluorosilicate equilibria followed by potentiometric titration;; products not isolated;

10193-36-9Relevant articles and documents

Structural and Photoluminescence properties of nepheline-structure NaAlSiO4:Dy3+ nanophosphors

Kumar, Ashwini,Dhoble,Peshwe,Bhatt, Jatin

, p. 100 - 106 (2014)

Most of the phosphors are composed of known host material with the incorporation of some percentage of an activator into the matrix. In this work Dy3+-activated NaAlSiO4 phosphors have been synthesized using sol-gel combustion techni

Paralinear oxidation of silicon nitride in a water-vapor/oxygen environment

Fox, Dennis S.,Opila, Elizabeth J.,Nguyen, Quynh Giao N.,Humphrey, Donald L.,Lewton, Susan M.

, p. 1256 - 1261 (2003)

Three Si3N4 materials were exposed to dry oxygen flowing at 0.44 cm/s at temperatures between 1200° and 1400°C. Weight change was measured using a continuously recording microbalance. Parabolic kinetics were observed. When the same materials were exposed to a 50% H2O-5% O2 gas mixture flowing at 4.4 cm/s, all three types exhibited paralinear kinetics. The material was oxidized by water vapor to form solid SiO2. The protective SiO2 was in turn volatilized by water vapor to form primarily gaseous Si(OH)4. Nonlinear least-squares analysis and a paralinear kinetic model were used to determine parabolic and linear rate constants from the kinetic data. Volatilization of the protective SiO2 scale could result in accelerated consumption of Si3N4. Recession rates under conditions more representative of actual combustors were compared with the furnace data.

Controlled growth of in situ silica in a NR/CR blend by a solution sol-gel method and the studies of its composite properties

Bansod, Naresh D.,Kapgate, Bharat P.,Das, Chayan,Basu, Debdipta,Debnath, Subhas Chandra,Roy, Kumarjyoti,Wiessner, Sven

, p. 53559 - 53568 (2015)

Silica is grown in situ into a natural rubber (NR)/chloroprene rubber (CR) blend (at 40/60 ratio), by a solution sol-gel method, where the silica content in rubber blend is increased in a controlled manner exceeding the limit found for the same blend ratio in the soaking sol-gel method. Reaction conditions have been optimized to get adequate conversion of tetraethoxysilane (TEOS, a silica precursor) to silica. Rheological, thermal, mechanical and viscoelastic properties of all the composites are compared with those of the unfilled rubber blend at similar conditions. Thermal and mechanical properties of the composites are found to improve consistently as silica content in the composite increases owing to increased rubber-filler interaction as revealed in dynamical mechanical analysis (DMA). Further improvement in the properties is observed for a particular composite where a silane coupling agent ((γ-aminopropyl)trimethoxysilane, γ-APS) is used in the reactive sol-gel system during in situ generation of silica. This is attributed to the uniform distribution of silica in the rubber matrix and strong rubber-filler interaction, caused by bifunctionality of silane, as revealed by morphology and DMA studies respectively. The reinforcement effect of silica is evaluated by comparing the experimental results with theoretical values obtained from the Guth-Gold model and the modified Guth model. The present study supplements the in situ silica generation in NR/CR blend of 40/60 ratio, following the solution sol-gel method, to the earlier study involving the soaking sol-gel method where the maximum reinforcement was found for this composition.

Zirconium phosphate combined with Ru/C as a highly efficient catalyst for the direct transformation of cellulose to C6 alditols

Liao, Yuhe,Liu, Qiying,Wang, Tiejun,Long, Jinxing,Ma, Longlong,Zhang, Qi

, p. 3305 - 3312 (2014)

The selective transformation of cellulose to C6 alditols provides a feasible route towards the sustainable synthesis of chemicals and fuels. Herein, the catalytic performance of amorphous zirconium phosphate (ZPA) combined with 5 wt% Ru/C was evaluated in the direct conversion of cellulose to C6 alditols (sorbitol and mannitol) under hydrothermal conditions. The yield of C6 alditols reached 63.5% and 85.5% with microcrystalline cellulose and ball-milled cellulose as the feedstock, respectively. This hybrid catalyst was developed to convert concentrated cellulose to obtain C6 alditols with a high concentration of 68.8 mg mL-1 in the final products. The high yield of C6 alditols from cellulose was ascribed to the fact that ZPA favoured the adsorption of cellulose and promoted its depolymerization to cellobiose and glucose, which was hydrogenated immediately to C6 alditols over Ru/C. The weak adsorption of C6 alditols over ZPA inhibited the dehydration of C6 alditols to sorbitan. Furthermore, ZPA exhibited excellent hydrothermal stability and could be reused for several runs. This journal is the Partner Organisations 2014.

Influence of annealing temperature on structural and optical properties of SiO2:RE2O3 [RE = Y, Gd] powder

Ahlawat, Rachna

, p. 356 - 363 (2015)

SiO2:RE2O3 [RE = Y, Gd] powder were prepared by wet chemical technique and the prepared binary oxides annealed at 500 °C and 900 °C. The crystalline structure, phase transformation, and surface morphologies of as-prepared and annealed samples were investigated by XRD and TEM. The normal transmission was measured using FTIR spectroscopy. Optical properties have been studied with UV-Vis spectroscopy and PL study. XRD results shows that the as prepared samples of SiO2:RE2O3 [RE = Y, Gd] powder has mixed phases of RE(NO3)3 and Si(OH)3. However, cubic rare earth oxide phase alone is found for annealed samples. The strain values are calculated from W-H plot for annealed samples. TEM micrograph shows that the samples are composed of individual spherical nanocrystallites at 500 °C and aggregated nanocrystallites at 900 °C. From the UV-Vis spectra, it is found that the position of the absorption peak is shifted toward the higher wavelength side when annealing temperature is increased. In the PL spectra, the broad emission bands are observed between 570-600 nm and the presence of O-Si-O (silica) and metal oxide is confirmed by FTIR spectra.

Interactions of water vapor with oxides at elevated temperatures

Jacobson, Nathan,Myers, Dwight,Opila, Elizabeth,Copland, Evan

, p. 471 - 478 (2005)

Many volatile metal hydroxides form by reaction of the corresponding metal oxide with water vapor. These reactions are important in a number of high temperature corrosion processes. Experimental methods for studying the thermodynamics of metal hydroxides include: gas leak Knudsen cell mass spectrometry, free jet sampling mass spectrometry, transpiration and hydrogen-oxygen flame studies. The available experimental information is reviewed and the most stable metal hydroxide species are correlated with position in the periodic table. Current studies in our laboratory on the Si-O-H system are discussed.

Ionic Liquid-Hybrid Molecularly Imprinted Material-Filter Solid-Phase Extraction Coupled with HPLC for Determination of 6-Benzyladenine and 4-Chlorophenoxyacetic Acid in Bean Sprouts

Han, Yehong,Yang, Chunliu,Zhou, Yang,Han, Dandan,Yan, Hongyuan

, p. 1750 - 1757 (2017)

A new method involving ionic liquid-hybrid molecularly imprinted material-filter solid-phase extraction coupled to high-performance liquid chromatography (IL-HIM-FSPE-HPLC) was developed for the simultaneous isolation and determination of 6-benzyladenine (6-BA) and 4-chlorophenoxyacetic acid (4-CPA) in bean sprouts. Sample preconcentration was performed using a modified filter, with the new IL-HIM as the adsorbent, which shows double adsorption. The first adsorption involves special recognition of molecular imprinting, and the second involves ion exchange and electrostatic attraction caused by the ionic liquid. This method combines the advantages of ionic liquids, hybrid materials, and molecularly imprinted polymers and was successfully applied to determine 6-BA and 4-CPA in bean sprouts. The adsorption of 6-BA to IL-HIM is based on selective imprinted recognition, whereas the adsorption of 4-CPA is mainly dependent on ion-exchange interactions.

Near-infrared spectroscopic study of [AlO4Al12(OH)23(H2O)12]7+-O-Si(OH)3 nitrate crystals formed by forced hydrolysis of Al3+ in the presence of TEOS.

Kloprogge,Ruan,Frost

, p. 2405 - 2411 (2000)

The polymer [AlO4Al12(OH)23(H2O)12]7+-O-Si(OH)3 was prepared by forced hydrolysis of Al3+ up to an OH/Al molar ratio of 2.0 in the presence of monomeric orthosilicic acid. Crystalline material was obtained by slow evaporation. Although the near-infrared spectra of the Al13-sulfate and Al13-O-Si(OH)3 are very similar, there are differences related to the bonding of the -O-Si(OH)3 group to the Al13-unit. The strong complex of bands around 7000 cm(-1) associated with the overtones and combination bands of the OH-stretching modes for Al13-sulfate is much weaker for Al13-O-Si(OH)3 and the opposite is true for the complex of bands around 5000 cm(-1) associated with the water overtone and combination modes, suggesting that the outer OH-groups of the Al13-unit are involved in the formation of the new Al13-O-Si(OH)3 units. A weak band around 7370-7631 cm(-1) is interpreted as the overtone of the Si-OH stretching vibration around 3740 cm(-1). A low intensity band, absent for Al13-sulfate and -nitrate is observed around 5550-5570 cm(-1) and is interpreted as the overtone of the OH-stretching mode of the OH-groups in the vicinity of the central AlO4 in the Al13-unit around 2890-2935 cm(-1). The interaction between the -O-Si(OH)3 group and the Al13-unit has a small influence on other bands like the combination modes of water in the 4400-4800 cm(-1) region, which show a small shift towards higher wavenumbers. The internal OH-groups in the Al13-complex are relatively shielded by the water molecules and therefore do not reflect the influence of the -O-Si(OH)3 in their band positions.

Morphosynthesis of complex inorganic forms using pollen grain templates.

Hall, Simon R,Bolger, Helen,Mann, Stephen

, p. 2784 - 2785 (2003)

Porous micron-sized particles of silica, calcium carbonate or calcium phosphate are prepared with complex morphologies by template-directed synthesis employing intact pollen grains; the materials adsorb and release drug molecules and can be functionalized

Effect of polyethylenimine on hydrolysis and dispersion properties of aqueous Si3N4 suspensions

Zhu, Xinwen,Uchikoshi, Tetsuo,Suzuki, Tohru S.,Sakka, Yoshio

, p. 797 - 804 (2007)

The roles of polyethylenimine (PEI) in the hydrolysis and dispersion properties of aqueous Si3-N4 suspensions were studied in terms of the hydrolysis, adsorption, electrokinetic, and rheological measurements. It was found that the pH change of the suspensions in the acidic environment could be minimized in the presence of ≥ 0.5 dwb% PEI. The ammonia and oxygen measurements suggest that this phenomenon is primarily attributed to the buffer mechanism generated by the ionized PEI, instead of the protection mechanism. The constant pH enables the suspensions to retain a better stability with time at acidic pH. The adsorption of PEI on Si3N4 is a high-affinity type at highly basic pH, but is a low-affinity type at acidic pH. As the PEI amount increases, the adsorption shifts the isoelectric point (IEP) of Si3N4 from pH 5.9 to pH ~11 until complete coverage is attained. The stability of Si3N4 suspensions is found to depend strongly on the saturated adsorption of PEI, which is as a function of the pH and PEI amount. Once the saturated adsorption limit is reached, the excess free PEI molecules become more detrimental to the stability with increased solid loading. The stabilization mechanisms of Si 3N4 suspensions by PEI were discussed in detail.

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