DD140667A5 - Verfahren zum herstellen von hydrophobem siliciumdioxyd - Google Patents

Verfahren zum herstellen von hydrophobem siliciumdioxyd Download PDF

Info

Publication number: DD140667A5
Authority: DD; German Democratic Republic
Prior art keywords: tin; silica; radicals; compound; silicon
Prior art date: 1977-12-07

Application number

DD78209389A

Other languages

German (de)

English (en)

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

1978-11-29

Publication date

1980-03-19

1978-11-29 Application filed by Wacker Chemie Gmbh filed Critical Wacker Chemie Gmbh

1980-03-19 Publication of DD140667A5 publication Critical patent/DD140667A5/de

Links

230000002209 hydrophobic effect Effects 0.000 title claims description 9
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title claims description 8
229910052710 silicon Inorganic materials 0.000 title claims description 5
239000010703 silicon Substances 0.000 title claims 2
238000004519 manufacturing process Methods 0.000 title description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 53
239000000377 silicon dioxide Substances 0.000 claims description 26
150000003606 tin compounds Chemical class 0.000 claims description 18
238000000034 method Methods 0.000 claims description 16
-1 tin halide Chemical group 0.000 claims description 16
150000003961 organosilicon compounds Chemical class 0.000 claims description 12
239000004215 Carbon black (E152) Substances 0.000 claims description 8
229930195733 hydrocarbon Natural products 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
229920006395 saturated elastomer Polymers 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 3
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 2
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
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 8
235000012239 silicon dioxide Nutrition 0.000 description 7
239000000203 mixture Substances 0.000 description 6
238000012986 modification Methods 0.000 description 6
230000004048 modification Effects 0.000 description 6
125000004432 carbon atom Chemical group C* 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
229910021627 Tin(IV) chloride Inorganic materials 0.000 description 4
239000002253 acid Substances 0.000 description 4
239000000945 filler Substances 0.000 description 4
HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 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
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
229920001971 elastomer Polymers 0.000 description 3
239000007789 gas Substances 0.000 description 3
150000003254 radicals Chemical class 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
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
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
230000000052 comparative effect Effects 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
WCRDXYSYPCEIAK-UHFFFAOYSA-N dibutylstannane Chemical compound CCCC[SnH2]CCCC WCRDXYSYPCEIAK-UHFFFAOYSA-N 0.000 description 2
238000001035 drying Methods 0.000 description 2
239000000806 elastomer Substances 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000011521 glass Substances 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
238000009413 insulation Methods 0.000 description 2
239000006224 matting agent Substances 0.000 description 2
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000003973 paint Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000002510 pyrogen Substances 0.000 description 2
229920001169 thermoplastic Polymers 0.000 description 2
239000004416 thermosoftening plastic Substances 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
SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 description 1
JLIJUQBAUMUMJK-UHFFFAOYSA-N 3-ethoxy-3-methylpentane Chemical compound CCOC(C)(CC)CC JLIJUQBAUMUMJK-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
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-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
YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 description 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
AJDTZVRPEPFODZ-PAMPIZDHSA-J [Sn+4].[O-]C(=O)\C=C/C([O-])=O.[O-]C(=O)\C=C/C([O-])=O Chemical compound [Sn+4].[O-]C(=O)\C=C/C([O-])=O.[O-]C(=O)\C=C/C([O-])=O AJDTZVRPEPFODZ-PAMPIZDHSA-J 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
YVHDRFKHKGNLNW-UHFFFAOYSA-L [dibutyl(octadecanoyloxy)stannyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCCCCCCCC YVHDRFKHKGNLNW-UHFFFAOYSA-L 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
150000005840 aryl radicals Chemical class 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
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
RGCPMRIOBZXXBR-UHFFFAOYSA-N butan-1-olate;dibutyltin(2+) Chemical compound CCCCO[Sn](CCCC)(CCCC)OCCCC RGCPMRIOBZXXBR-UHFFFAOYSA-N 0.000 description 1
RSVHRUAXLBHWLD-UHFFFAOYSA-N butyl hypochlorite;dibutyltin Chemical compound CCCCOCl.CCCC[Sn]CCCC RSVHRUAXLBHWLD-UHFFFAOYSA-N 0.000 description 1
150000001723 carbon free-radicals Chemical class 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
MYSWGUAQZAJSOK-UHFFFAOYSA-N ciprofloxacin Chemical compound C12=CC(N3CCNCC3)=C(F)C=C2C(=O)C(C(=O)O)=CN1C1CC1 MYSWGUAQZAJSOK-UHFFFAOYSA-N 0.000 description 1
239000000470 constituent Substances 0.000 description 1
RJGHQTVXGKYATR-UHFFFAOYSA-L dibutyl(dichloro)stannane Chemical compound CCCC[Sn](Cl)(Cl)CCCC RJGHQTVXGKYATR-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
ZXDVQYBUEVYUCG-UHFFFAOYSA-N dibutyltin(2+);methanolate Chemical compound CCCC[Sn](OC)(OC)CCCC ZXDVQYBUEVYUCG-UHFFFAOYSA-N 0.000 description 1
DWGCJJZWHKUSLC-UHFFFAOYSA-N diethoxy(dimethyl)stannane Chemical compound CCO[Sn](C)(C)OCC DWGCJJZWHKUSLC-UHFFFAOYSA-N 0.000 description 1
229920005645 diorganopolysiloxane polymer Polymers 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
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
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
238000002309 gasification Methods 0.000 description 1
238000000227 grinding 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
FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 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
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
238000010902 jet-milling Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
KJGLZJQPMKQFIK-UHFFFAOYSA-N methanolate;tributylstannanylium Chemical compound CCCC[Sn](CCCC)(CCCC)OC KJGLZJQPMKQFIK-UHFFFAOYSA-N 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000005609 naphthenate group Chemical group 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229920001568 phenolic resin Polymers 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
CCTFOFUMSKSGRK-UHFFFAOYSA-N propan-2-olate;tin(4+) Chemical compound [Sn+4].CC(C)[O-].CC(C)[O-].CC(C)[O-].CC(C)[O-] CCTFOFUMSKSGRK-UHFFFAOYSA-N 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
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
TWRYZRQZQIBEIE-UHFFFAOYSA-N tetramethoxystannane Chemical compound [Sn+4].[O-]C.[O-]C.[O-]C.[O-]C TWRYZRQZQIBEIE-UHFFFAOYSA-N 0.000 description 1
229920001187 thermosetting polymer Polymers 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
ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical compound C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 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)

DD78209389A 1977-12-07 1978-11-29 Verfahren zum herstellen von hydrophobem siliciumdioxyd DD140667A5 (de)

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
DD140667A5 true DD140667A5 (de)	1980-03-19

Family

ID=6025510

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD78209389A DD140667A5 (de)	1977-12-07	1978-11-29	Verfahren zum herstellen von hydrophobem 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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DE3839900A1 (de) *	1988-11-25	1990-05-31	Wacker Chemie Gmbh	Verfahren zur hydrophobierung von si-oh-gruppen enthaltendem, teilchenfoermigem feststoff und verwendung des erhaltenen, hydrophoben, teilchenfoermigen feststoffes in einem verfahren zur herstellung von zu elastomeren haertbaren massen auf basis von diorganopolysiloxanen
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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
NO784111L (no)	1979-06-08
US4191587A (en)	1980-03-04
FR2411157A1 (fr)	1979-07-06
IT7852195A0 (it)	1978-12-05
AU4222878A (en)	1979-06-14
GB2009719B (en)	1982-04-28

Publication	Publication Date	Title
DD140667A5 (de)	1980-03-19	Verfahren zum herstellen von hydrophobem siliciumdioxyd
DE2641353B2 (de)	1978-07-06	Additiv zur Beeinflussung der Fließeigenschaften von nichtwäßrigen fluiden Systemen
EP2220172B1 (fr)	2016-03-02	Hydrophobation de silices en conditions oxydantes
DE1284547B (de)	1968-12-05	Verfahren zur Herstellung hydrophober, feinverteilter, nicht alkalischer Fuellstoffe oder Pigmente
EP0050358B1 (fr)	1985-03-20	Agent de réticulation basé sur un produit de réaction entre des esters d'acide silicique et des composés d'organoétain et procédé pour l'obtention des élastomères polysiloxaniques
DE2660040C3 (de)	1983-05-11	Organozinnverbindungen und deren Verwendung als Stabilisatoren
DE1768588B1 (de)	1971-05-27	Verfahren zur Alkylierung von Silicium- und Zinnderivaten
DE1230154B (de)	1966-12-08	Mit Titandioxid pigmentierte Polysiloxanlacke
DE1544913A1 (de)	1969-07-31	Stabilisierendes Mittel gegenueber Einfluessen von Waerme und Feuchtigkeit in estergruppenhaltigen Kunststoffen
EP0579232B1 (fr)	1995-04-19	Procédé pour augmenter le point d'éclair d'organopolysiloxanes ayant des groupes à liaison SiOC
DE69218639T2 (de)	1997-08-21	Silikon-Kautschukzusammensetzung
DE2148774A1 (de)	1972-04-06	Stabilisatoren fuer Vinylchloridharze
DE2257645A1 (de)	1973-05-30	Flammhemmende und bei raumtemperatur vulkanisierende organopolysiloxan-zusammensetzungen
DD299187A5 (de)	1992-04-02	Verfahren zur Herstellung von schwefelhaltigen Organosiliciumverbindungen
EP0039008B1 (fr)	1983-05-25	Compositions de revêtement
DE1260793B (de)	1968-02-08	Verfahren zur Polymerisation von olefinischen ungesaettigten, organischen Verbindungen
DE1152413C2 (de)	1976-02-05	Verfahren zur herstellung von organozinnverbindungen
DE2558408B2 (de)	1980-10-09	Verfahren zum Stabilisieren von chlorhaltigen Polymerisaten
AT226247B (de)	1963-03-11	Verfahren zur Herstellung von Organozinnverbindungen
DE2902646C2 (de)	1982-04-08	Bis-trialkylstannylderivate chlorierter polycyclischer Dicarbonsäuren, Verfahren zu ihrer Herstellung und Mittel für Aufwuchsverhütungsüberzüge
CH631426A5 (en)	1982-08-13	Process for binding inorganic materials
DE2543849B2 (fr)	1979-05-10
DE1903904C3 (de)	1977-09-08	Verwendung von hydrophoben Füllstoffen für zu Elastomeren härtbare Massen auf Grundlage von Diorganopolysiloxanen
AT233841B (de)	1964-05-25	Lichtstabilisator für Kunstharze, Kunststoffe und Lacke auf Basis von Polyvinylchlorid, Polyestern und Celluloseestern
DE1195052B (de)	1965-06-16	Verfahren zur Herstellung von hydroxyliertem Polyaethylen