NO784111L - Fremgangsmaate ved fremstilling av hydrofobt siliciumdioxyd - Google Patents

Fremgangsmaate ved fremstilling av hydrofobt siliciumdioxyd

Info

Publication number: NO784111L
Authority: NO; Norway
Prior art keywords: tin; silicon dioxide; compound; silicon; groups
Prior art date: 1977-12-07

Application number

NO784111A

Other languages

English (en)

Norwegian (no)

Inventor

Guenter Kratel

Guenter Stohr

Hans Katzer

Original Assignee

Wacker Chemie Gmbh

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1977-12-07

Filing date

1978-12-06

Publication date

1979-06-08

1978-12-06 Application filed by Wacker Chemie Gmbh filed Critical Wacker Chemie Gmbh

1979-06-08 Publication of NO784111L publication Critical patent/NO784111L/no

Links

238000000034 method Methods 0.000 title claims abstract description 20
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 54
239000000377 silicon dioxide Substances 0.000 claims abstract description 27
230000002209 hydrophobic effect Effects 0.000 claims abstract description 6
238000004519 manufacturing process Methods 0.000 claims abstract description 3
235000012239 silicon dioxide Nutrition 0.000 claims description 26
150000003606 tin compounds Chemical class 0.000 claims description 17
150000003961 organosilicon compounds Chemical class 0.000 claims description 12
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 9
229910052736 halogen Inorganic materials 0.000 claims description 7
150000002367 halogens Chemical class 0.000 claims description 7
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical group [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 6
229920006395 saturated elastomer Polymers 0.000 claims description 6
229910052710 silicon Inorganic materials 0.000 claims description 6
150000001875 compounds Chemical class 0.000 claims description 3
125000000962 organic group Chemical group 0.000 claims description 3
239000010703 silicon Substances 0.000 claims description 3
125000001183 hydrocarbyl group Chemical group 0.000 claims 2
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 9
150000002430 hydrocarbons Chemical group 0.000 description 6
WCRDXYSYPCEIAK-UHFFFAOYSA-N dibutylstannane Chemical compound CCCC[SnH2]CCCC WCRDXYSYPCEIAK-UHFFFAOYSA-N 0.000 description 5
HTDJPCNNEPUOOQ-UHFFFAOYSA-N hexamethylcyclotrisiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O1 HTDJPCNNEPUOOQ-UHFFFAOYSA-N 0.000 description 5
239000000203 mixture Substances 0.000 description 5
238000001035 drying Methods 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
239000002253 acid Substances 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
239000000945 filler Substances 0.000 description 3
239000007789 gas Substances 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
229910021627 Tin(IV) chloride Inorganic materials 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
229920001971 elastomer Polymers 0.000 description 2
239000011521 glass Substances 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000002156 mixing Methods 0.000 description 2
HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
ODIGIKRIUKFKHP-UHFFFAOYSA-N (n-propan-2-yloxycarbonylanilino) acetate Chemical group CC(C)OC(=O)N(OC(C)=O)C1=CC=CC=C1 ODIGIKRIUKFKHP-UHFFFAOYSA-N 0.000 description 1
VMAWODUEPLAHOE-UHFFFAOYSA-N 2,4,6,8-tetrakis(ethenyl)-2,4,6,8-tetramethyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical compound C=C[Si]1(C)O[Si](C)(C=C)O[Si](C)(C=C)O[Si](C)(C=C)O1 VMAWODUEPLAHOE-UHFFFAOYSA-N 0.000 description 1
NQEZDDPEJMKMOS-UHFFFAOYSA-N 4-trimethylsilylbut-3-yn-2-one Chemical compound CC(=O)C#C[Si](C)(C)C NQEZDDPEJMKMOS-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
MKUWNMKVSHFQJR-UHFFFAOYSA-H COC(=O)[Sn+2]C1=CC=CC=C1.COC(=O)[Sn+2]C1=CC=CC=C1.COC(=O)[Sn+2]C1=CC=CC=C1.[O-]C(=O)CCCCCCC([O-])=O.[O-]C(=O)CCCCCCC([O-])=O.[O-]C(=O)CCCCCCC([O-])=O Chemical compound COC(=O)[Sn+2]C1=CC=CC=C1.COC(=O)[Sn+2]C1=CC=CC=C1.COC(=O)[Sn+2]C1=CC=CC=C1.[O-]C(=O)CCCCCCC([O-])=O.[O-]C(=O)CCCCCCC([O-])=O.[O-]C(=O)CCCCCCC([O-])=O MKUWNMKVSHFQJR-UHFFFAOYSA-H 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
JJLKTTCRRLHVGL-UHFFFAOYSA-L [acetyloxy(dibutyl)stannyl] acetate Chemical compound CC([O-])=O.CC([O-])=O.CCCC[Sn+2]CCCC JJLKTTCRRLHVGL-UHFFFAOYSA-L 0.000 description 1
NSJFNSBWVWFNHJ-UHFFFAOYSA-L [acetyloxy-bis(ethenyl)stannyl] acetate Chemical compound CC([O-])=O.CC([O-])=O.C=C[Sn+2]C=C NSJFNSBWVWFNHJ-UHFFFAOYSA-L 0.000 description 1
LHFURYICKMKJHJ-UHFFFAOYSA-L [benzoyloxy(dibutyl)stannyl] benzoate Chemical compound CCCC[Sn+2]CCCC.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 LHFURYICKMKJHJ-UHFFFAOYSA-L 0.000 description 1
HAAANJSJNWKVMX-UHFFFAOYSA-L [butanoyloxy(dimethyl)stannyl] butanoate Chemical compound CCCC(=O)O[Sn](C)(C)OC(=O)CCC HAAANJSJNWKVMX-UHFFFAOYSA-L 0.000 description 1
150000007513 acids Chemical group 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
KPMOFDIAYWNUGA-UHFFFAOYSA-L bis(3-methylbutyl)tin(2+);2,3,4-trichlorobenzoate Chemical compound CC(C)CC[Sn+2]CCC(C)C.[O-]C(=O)C1=CC=C(Cl)C(Cl)=C1Cl.[O-]C(=O)C1=CC=C(Cl)C(Cl)=C1Cl KPMOFDIAYWNUGA-UHFFFAOYSA-L 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
RSVHRUAXLBHWLD-UHFFFAOYSA-N butyl hypochlorite;dibutyltin Chemical compound CCCCOCl.CCCC[Sn]CCCC RSVHRUAXLBHWLD-UHFFFAOYSA-N 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
RJGHQTVXGKYATR-UHFFFAOYSA-L dibutyl(dichloro)stannane Chemical compound CCCC[Sn](Cl)(Cl)CCCC RJGHQTVXGKYATR-UHFFFAOYSA-L 0.000 description 1
PFEOYOVWDZZLPS-UHFFFAOYSA-L dibutyltin(2+);2-hydroxypropanoate Chemical compound CC(O)C([O-])=O.CC(O)C([O-])=O.CCCC[Sn+2]CCCC PFEOYOVWDZZLPS-UHFFFAOYSA-L 0.000 description 1
SGIBEPSSERDAHS-UHFFFAOYSA-L dibutyltin(2+);hexanedioate Chemical compound CCCC[Sn+2]CCCC.[O-]C(=O)CCCCC([O-])=O SGIBEPSSERDAHS-UHFFFAOYSA-L 0.000 description 1
PWEVMPIIOJUPRI-UHFFFAOYSA-N dimethyltin Chemical compound C[Sn]C PWEVMPIIOJUPRI-UHFFFAOYSA-N 0.000 description 1
229920005645 diorganopolysiloxane polymer Polymers 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000000806 elastomer Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
WDQNIWFZKXZFAY-UHFFFAOYSA-M fentin acetate Chemical compound CC([O-])=O.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1 WDQNIWFZKXZFAY-UHFFFAOYSA-M 0.000 description 1
239000012530 fluid Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
238000002309 gasification Methods 0.000 description 1
UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
239000000017 hydrogel Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
239000012774 insulation material Substances 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000006224 matting agent Substances 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229940049964 oleate Drugs 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000010025 steaming Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
TUCCZSRGFGBTOQ-UHFFFAOYSA-J terephthalate;tin(4+) Chemical compound [Sn+4].[O-]C(=O)C1=CC=C(C([O-])=O)C=C1.[O-]C(=O)C1=CC=C(C([O-])=O)C=C1 TUCCZSRGFGBTOQ-UHFFFAOYSA-J 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
229920001187 thermosetting polymer Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
PIILXFBHQILWPS-UHFFFAOYSA-N tributyltin Chemical compound CCCC[Sn](CCCC)CCCC PIILXFBHQILWPS-UHFFFAOYSA-N 0.000 description 1
GLAUZTOWUMJVND-UHFFFAOYSA-M tricyclohexylstannyl prop-2-enoate Chemical compound C1CCCCC1[Sn](C1CCCCC1)(OC(=O)C=C)C1CCCCC1 GLAUZTOWUMJVND-UHFFFAOYSA-M 0.000 description 1
CPRPKIMXLHBUGA-UHFFFAOYSA-N triethyltin Chemical compound CC[Sn](CC)CC CPRPKIMXLHBUGA-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/28—Compounds of silicon
- C09C1/30—Silicic acid
- C09C1/309—Combinations of treatments provided for in groups C09C1/3009 - C09C1/3081
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/06—Treatment with inorganic compounds
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/08—Treatment with low-molecular-weight non-polymer organic compounds
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/12—Treatment with organosilicon compounds
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/12—Surface area
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/90—Other properties not specified above
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
- Y10T428/2993—Silicic or refractory material containing [e.g., tungsten oxide, glass, cement, etc.]
- Y10T428/2995—Silane, siloxane or silicone coating

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)
Silicon Compounds (AREA)
Silicon Polymers (AREA)

NO784111A 1977-12-07 1978-12-06 Fremgangsmaate ved fremstilling av hydrofobt siliciumdioxyd NO784111L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2754484A DE2754484C2 (de)	1977-12-07	1977-12-07	Verfahren zum Herstellen von hydrophobem Siliciumdioxyd

Publications (1)

Publication Number	Publication Date
NO784111L true NO784111L (no)	1979-06-08

Family

ID=6025510

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO784111A NO784111L (no)	1977-12-07	1978-12-06	Fremgangsmaate ved fremstilling av hydrofobt siliciumdioxyd

Country Status (13)

Country	Link
US (1)	US4191587A (fr)
JP (1)	JPS5486540A (fr)
AU (1)	AU4222878A (fr)
BE (1)	BE872560A (fr)
CA (1)	CA1110933A (fr)
DD (1)	DD140667A5 (fr)
DE (1)	DE2754484C2 (fr)
FR (1)	FR2411157A1 (fr)
GB (1)	GB2009719B (fr)
IT (1)	IT1106365B (fr)
NL (1)	NL7811625A (fr)
NO (1)	NO784111L (fr)
SE (1)	SE7812575L (fr)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS54101795A (en) *	1978-01-30	1979-08-10	Toyo Soda Mfg Co Ltd	Hydrophobic rendering method for oxide fine powder
JPS55154354A (en) *	1979-05-16	1980-12-01	Toray Silicone Co Ltd	Silicone composition for treating glass fiber
DE2927379A1 (de) *	1979-07-06	1981-01-08	Bayer Ag	Feinteilige festkoerper, ihre herstellung und verwendung
US4398954A (en) *	1979-12-31	1983-08-16	The Mead Corporation	Microcapsular coating composition containing a hydrophobic silica
US4268069A (en) *	1979-12-31	1981-05-19	The Mead Corporation	Paper coated with a microcapsular coating composition containing a hydrophobic silica
US4529774A (en) *	1982-08-20	1985-07-16	General Electric Company	Treated silica fillers and process for making same
US4584243A (en) *	1982-11-01	1986-04-22	Sumitomo Chemical Company, Limited	Abrasive, production thereof and use thereof in magnetic recording medium
JPS5982633A (ja) *	1982-11-02	1984-05-12	Sumitomo Chem Co Ltd	親油性表面を有する磁気記録用研磨剤
JPS60201359A (ja) *	1984-03-27	1985-10-11	Ricoh Co Ltd	静電潜像現像剤用キヤリア
US4818614A (en) *	1985-07-29	1989-04-04	Shiseido Company Ltd.	Modified powder
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1977
- 1977-12-07 DE DE2754484A patent/DE2754484C2/de not_active Expired
1978
- 1978-11-27 NL NL7811625A patent/NL7811625A/xx not_active Application Discontinuation
- 1978-11-29 DD DD78209389A patent/DD140667A5/de unknown
- 1978-11-30 US US05/965,537 patent/US4191587A/en not_active Expired - Lifetime
- 1978-12-05 AU AU42228/78A patent/AU4222878A/en active Pending
- 1978-12-05 IT IT52195/78A patent/IT1106365B/it active
- 1978-12-05 GB GB7847229A patent/GB2009719B/en not_active Expired
- 1978-12-06 FR FR7834323A patent/FR2411157A1/fr active Granted
- 1978-12-06 NO NO784111A patent/NO784111L/no unknown
- 1978-12-06 CA CA317,489A patent/CA1110933A/fr not_active Expired
- 1978-12-06 BE BE192165A patent/BE872560A/fr unknown
- 1978-12-06 SE SE7812575A patent/SE7812575L/xx unknown
- 1978-12-06 JP JP15015378A patent/JPS5486540A/ja active Granted

Also Published As

Publication number	Publication date
DE2754484C2 (de)	1983-07-21
IT1106365B (it)	1985-11-11
FR2411157B1 (fr)	1980-07-04
BE872560A (fr)	1979-06-06
GB2009719A (en)	1979-06-20
DE2754484A1 (de)	1979-06-13
JPS5717844B2 (fr)	1982-04-13
CA1110933A (fr)	1981-10-20
SE7812575L (sv)	1979-06-08
JPS5486540A (en)	1979-07-10
NL7811625A (nl)	1979-06-11
US4191587A (en)	1980-03-04
FR2411157A1 (fr)	1979-07-06
IT7852195A0 (it)	1978-12-05
DD140667A5 (de)	1980-03-19
AU4222878A (en)	1979-06-14
GB2009719B (en)	1982-04-28

Publication	Publication Date	Title
NO784111L (no)	1979-06-08	Fremgangsmaate ved fremstilling av hydrofobt siliciumdioxyd
GB932753A (en)	1963-07-31	Improvements in or relating to fillers and pigments by treatment with dihydrocarbyl polysiloxane
US4298753A (en)	1981-11-03	Continuous process for preparing silanes and siloxanes having SiOC groups
EP0017734B1 (fr)	1983-04-13	Compositions organopolysiloxane durcissables contenant du noir de fumée, procédé pour leur préparation et procédé pour durcir les compositions
US4177201A (en)	1979-12-04	Preparation of silicon-functional polyorganosiloxanes
DE2453482A1 (de)	1976-05-13	Verfahren zur herstellung von linearen und verzweigten chlorsiloxanen
EP0499407A1 (fr)	1992-08-19	Agents de réticulation et agents d'allongement pour la vulcanisation ou la réticulation des polymères à température ambiante
GB799917A (en)	1958-08-13	An improved process for producing cyclic diorganosiloxanes
EP0095157B1 (fr)	1986-08-06	Procédé de préparation de composés de silice ayant des groupes d'ammonium quaternaires, leurs dérivés et leur emploi
GB804097A (en)	1958-11-05	A process for the production of organosilicon compounds
US3516951A (en)	1970-06-23	Room temperature vulcanizing silicone rubber foam
GB804199A (en)	1958-11-12	Organosiloxane compositions
US5357016A (en)	1994-10-18	Preparation and processing of polydiorganosiloxanes
US3032529A (en)	1962-05-01	Stabilized organopolysiloxane resins
US3931047A (en)	1976-01-06	Catalyst composition for room temperature vulcanizing silicone compositions and catalyzed compositions therefrom
GB766528A (en)	1957-01-23	A process for the production of organosilicon compounds
US3565859A (en)	1971-02-23	Diorganopolysiloxane compositions curable on exposure to moisture
US5519158A (en)	1996-05-21	Method and apparatus for desiccant drying of fluorosilicones
US2562884A (en)	1951-08-07	Chlorination of carbohydrate ethers
US3231527A (en)	1966-01-25	Curing organopolysiloxanes with a combination of trichloroacetic acid andidibutylxtin
GB1081150A (en)	1967-08-31	Novel alkadienyl silanes and polysiloxanes and method of preparing the same
GB892782A (en)	1962-03-28	Process for the production of high-polymeric alkyl and aryl-siloxanes
US3931105A (en)	1976-01-06	Catalyst composition for room temperature vulcanizing silicone compositions and catalyzed compositions therefrom
JPH0291126A (ja)	1990-03-30	アルケニル基含有オルガノポリシロキサンの製造方法
GB848674A (en)	1960-09-21	Silicon dioxide pigments and preparation of same