CS255872B2 - Low-misted mixture in the form of components - Google Patents

Low-misted mixture in the form of components Download PDF

Info

Publication number: CS255872B2
Authority: CS; Czechoslovakia
Prior art keywords: weight; hden; dust; blue; arylhydroxypolyalkoxylate
Prior art date: 1985-05-02

Application number

CS863166A

Other languages

Czech (cs)

English (en)

Other versions

CS316686A2 (en

Inventor

George Hull

Original Assignee

Ici Plc

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.)

1985-05-02

Filing date

1986-04-30

Publication date

1988-03-15

1986-04-30 Application filed by Ici Plc filed Critical Ici Plc

1987-07-16 Publication of CS316686A2 publication Critical patent/CS316686A2/cs

1988-03-15 Publication of CS255872B2 publication Critical patent/CS255872B2/cs

Links

239000000203 mixture Substances 0.000 title claims abstract description 13
239000007787 solid Substances 0.000 claims abstract description 20
125000003118 aryl group Chemical group 0.000 claims abstract description 11
-1 2-phenylphenyl Chemical group 0.000 claims description 6
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 5
125000005529 alkyleneoxy group Chemical group 0.000 claims description 4
125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 2
125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
125000003944 tolyl group Chemical group 0.000 claims description 2
238000010410 dusting Methods 0.000 abstract description 2
239000004094 surface-active agent Substances 0.000 abstract description 2
239000000428 dust Substances 0.000 description 20
239000000126 substance Substances 0.000 description 12
239000000975 dye Substances 0.000 description 7
JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 6
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
238000000034 method Methods 0.000 description 6
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
239000000049 pigment Substances 0.000 description 5
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 4
238000007664 blowing Methods 0.000 description 4
CYHOWEBNQPOWEI-UHFFFAOYSA-L calcium 3-carboxy-1-phenyldiazenylnaphthalen-2-olate Chemical compound OC=1C(=CC2=CC=CC=C2C1N=NC1=CC=CC=C1)C(=O)[O-].OC=1C(=CC2=CC=CC=C2C1N=NC1=CC=CC=C1)C(=O)[O-].[Ca+2] CYHOWEBNQPOWEI-UHFFFAOYSA-L 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
239000011521 glass Substances 0.000 description 4
229950011260 betanaphthol Drugs 0.000 description 3
235000012745 brilliant blue FCF Nutrition 0.000 description 3
WRIILVBYWBDSMT-UHFFFAOYSA-N 1,3,6-trihydroxyxanthen-9-one Chemical compound OC1=CC(O)=C2C(=O)C3=CC=C(O)C=C3OC2=C1 WRIILVBYWBDSMT-UHFFFAOYSA-N 0.000 description 2
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
229940061334 2-phenylphenol Drugs 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 2
230000005660 hydrophilic surface Effects 0.000 description 2
239000007788 liquid Substances 0.000 description 2
QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
235000010292 orthophenyl phenol Nutrition 0.000 description 2
KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
239000000985 reactive dye Substances 0.000 description 2
GKAVWWCJCPVMNR-UHFFFAOYSA-N tridecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCC GKAVWWCJCPVMNR-UHFFFAOYSA-N 0.000 description 2
KOTVVDDZWMCZBT-UHFFFAOYSA-N vat violet 1 Chemical compound C1=CC=C[C]2C(=O)C(C=CC3=C4C=C(C=5C=6C(C([C]7C=CC=CC7=5)=O)=CC=C5C4=6)Cl)=C4C3=C5C=C(Cl)C4=C21 KOTVVDDZWMCZBT-UHFFFAOYSA-N 0.000 description 2
BLFZMXOCPASACY-UHFFFAOYSA-N 1,4-bis(propan-2-ylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(NC(C)C)=CC=C2NC(C)C BLFZMXOCPASACY-UHFFFAOYSA-N 0.000 description 1
YZSHPQIVDURXEH-UHFFFAOYSA-N 1-(2-chlorophenyl)-3,3-dimethyl-2-(2h-triazol-4-ylmethyl)butan-2-ol Chemical compound C=1C=CC=C(Cl)C=1CC(O)(C(C)(C)C)CC=1C=NNN=1 YZSHPQIVDURXEH-UHFFFAOYSA-N 0.000 description 1
XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 1
WCXGOVYROJJXHA-UHFFFAOYSA-N 3-[4-[4-(3-aminophenoxy)phenyl]sulfonylphenoxy]aniline Chemical compound NC1=CC=CC(OC=2C=CC(=CC=2)S(=O)(=O)C=2C=CC(OC=3C=C(N)C=CC=3)=CC=2)=C1 WCXGOVYROJJXHA-UHFFFAOYSA-N 0.000 description 1
239000005510 Diuron Substances 0.000 description 1
SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
239000000980 acid dye Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
239000000981 basic dye Substances 0.000 description 1
210000000941 bile Anatomy 0.000 description 1
239000003139 biocide Substances 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000003638 chemical reducing agent Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
NMCCNOZOBBWFMN-UHFFFAOYSA-N davicil Chemical compound CS(=O)(=O)C1=C(Cl)C(Cl)=NC(Cl)=C1Cl NMCCNOZOBBWFMN-UHFFFAOYSA-N 0.000 description 1
ZFAKTZXUUNBLEB-UHFFFAOYSA-N dicyclohexylazanium;nitrite Chemical compound [O-]N=O.C1CCCCC1[NH2+]C1CCCCC1 ZFAKTZXUUNBLEB-UHFFFAOYSA-N 0.000 description 1
239000000982 direct dye Substances 0.000 description 1
XWZDJOJCYUSIEY-UHFFFAOYSA-L disodium 5-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-hydroxy-3-phenyldiazenylnaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].Oc1c(N=Nc2ccccc2)c(cc2cc(cc(Nc3nc(Cl)nc(Cl)n3)c12)S([O-])(=O)=O)S([O-])(=O)=O XWZDJOJCYUSIEY-UHFFFAOYSA-L 0.000 description 1
OOYIOIOOWUGAHD-UHFFFAOYSA-L disodium;2',4',5',7'-tetrabromo-4,5,6,7-tetrachloro-3-oxospiro[2-benzofuran-1,9'-xanthene]-3',6'-diolate Chemical compound [Na+].[Na+].O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(Br)=C([O-])C(Br)=C1OC1=C(Br)C([O-])=C(Br)C=C21 OOYIOIOOWUGAHD-UHFFFAOYSA-L 0.000 description 1
239000000986 disperse dye Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
125000002950 monocyclic group Chemical group 0.000 description 1
IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000011236 particulate material Substances 0.000 description 1
125000003367 polycyclic group Chemical group 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
KUIXZSYWBHSYCN-UHFFFAOYSA-L remazol brilliant blue r Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=C2C(=O)C3=CC=CC=C3C(=O)C2=C1NC1=CC=CC(S(=O)(=O)CCOS([O-])(=O)=O)=C1 KUIXZSYWBHSYCN-UHFFFAOYSA-L 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
DJDYMAHXZBQZKH-UHFFFAOYSA-M sodium;1-amino-4-(cyclohexylamino)-9,10-dioxoanthracene-2-sulfonate Chemical compound [Na+].C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C(S([O-])(=O)=O)C=C1NC1CCCCC1 DJDYMAHXZBQZKH-UHFFFAOYSA-M 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000000984 vat dye Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0092—Dyes in solid form
- C09B67/0094—Treatment of powders, e.g. antidusting
- 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
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/22—Materials not provided for elsewhere for dust-laying or dust-absorbing
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/916—Natural fiber dyeing
- Y10S8/918—Cellulose textile

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Compositions Of Macromolecular Compounds (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pretreatment Of Seeds And Plants (AREA)
Cosmetics (AREA)
Manufacturing Of Micro-Capsules (AREA)

CS863166A 1985-05-02 1986-04-30 Low-misted mixture in the form of components CS255872B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB858511207A GB8511207D0 (en)	1985-05-02	1985-05-02	Particulate composition

Publications (2)

Publication Number	Publication Date
CS316686A2 CS316686A2 (en)	1987-07-16
CS255872B2 true CS255872B2 (en)	1988-03-15

Family

ID=10578569

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS863166A CS255872B2 (en)	1985-05-02	1986-04-30	Low-misted mixture in the form of components

Country Status (6)

Country	Link
US (1)	US4722736A (de)
EP (1)	EP0200388A3 (de)
JP (1)	JPS61254671A (de)
CS (1)	CS255872B2 (de)
DD (1)	DD250541A5 (de)
GB (2)	GB8511207D0 (de)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS649272A (en) *	1987-07-01	1989-01-12	Nippon Kayaku Kk	Non-flying granular dye
DE4406630A1 (de) *	1994-03-01	1995-09-07	Bayer Ag	Entstaubungsmittel
DE10244683A1 (de) *	2002-09-24	2004-04-01	Basf Ag	Feste Pigmentzubereitungen, enthaltend oberflächenaktive Additive auf Basis von alkoxylierten Bisphenolen
CN108601331B (zh) *	2016-02-19	2021-10-29	罗门哈斯公司	低尘动物垫料
EP4438609A1 (de)	2023-03-30	2024-10-02	LANXESS Organometallics GmbH	Hocheffizientes verfahren zur rückgewinnung und umwandlung von methylaluminoxanresten

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2348518B2 (de) *	1973-09-27	1978-06-29	Basf Ag, 6700 Ludwigshafen	Pulverförmige, hochkonzentrierte und dispersionsstabile Farbstoffzubereitungen und Verfahren zu deren Herstellung
DE2656407C3 (de) *	1976-12-13	1981-10-08	CIBA-GEIGY AG, 4002 Basel	Verfahren zur Herstellung von staubarmen Farbstoff- und optischen Aufhellerpräparaten und deren Verwendung
DE2656408C2 (de) *	1976-12-13	1983-12-15	CIBA-GEIGY AG, 4002 Basel	Verfahren zur Herstellung von staubarmen Präparaten und deren Verwendung
LU76632A1 (de) *	1977-01-24	1978-09-13
US4525170A (en) *	1982-05-27	1985-06-25	Ciba-Geigy Corporation	Solid formulations of metal complex dyes

1985
- 1985-05-02 GB GB858511207A patent/GB8511207D0/en active Pending
1986
- 1986-04-08 EP EP86302593A patent/EP0200388A3/de not_active Withdrawn
- 1986-04-09 GB GB868608653A patent/GB8608653D0/en active Pending
- 1986-04-15 US US06/852,112 patent/US4722736A/en not_active Expired - Fee Related
- 1986-04-30 DD DD86289818A patent/DD250541A5/de not_active IP Right Cessation
- 1986-04-30 CS CS863166A patent/CS255872B2/cs unknown
- 1986-04-30 JP JP61098441A patent/JPS61254671A/ja active Pending

Also Published As

Publication number	Publication date
DD250541A5 (de)	1987-10-14
EP0200388A3 (de)	1990-03-21
GB8608653D0 (en)	1986-05-14
GB8511207D0 (en)	1985-06-12
JPS61254671A (ja)	1986-11-12
US4722736A (en)	1988-02-02
CS316686A2 (en)	1987-07-16
EP0200388A2 (de)	1986-11-05

Publication	Publication Date	Title
Bird	1954	The dyeing of acetate rayon with disperse dyes I‐aqueous solubility and the influence of dispersing agents II‐the relation between aqueous solubility and dyeing properties
GB2045055A (en)	1980-10-29	Method of reducing the number of microorganisms in a medium and a method of preservation
US3840383A (en)	1974-10-08	Colored inorganic pigments
US4072570A (en)	1978-02-07	Preparation of a tuberculosis test medium by reconstituting a storage stabilized dry powdered Lowenstein-Jensen medium
US4328220A (en)	1982-05-04	Non-dusty pulverulent and granulated organic dye preparations
CS255872B2 (en)	1988-03-15	Low-misted mixture in the form of components
US2486562A (en)	1949-11-01	Nondusting water-soluble organic dyestuff and method of making same
GB2187746A (en)	1987-09-16	Hydroxyphenyl benzotriazole UV light absorber aqueous dispersions and their use in dyeing processes
US4673762A (en)	1987-06-16	Decolorizing ethanolamines with alkylene oxides
CN1090210C (zh)	2002-09-04	粒状隐色还原染料制剂
US2184617A (en)	1939-12-26	Stabilized cuprous oxide
GB1121367A (en)	1968-07-24	Readily dispersible inorganic pulverous compositions and process for their production
US2222225A (en)	1940-11-19	Method of and compositions for influencing the growth of plants
Manolkidis et al.	1971	Effects of some antibiotics on the milk phosphatase pasteurization test
CA1314140C (en)	1993-03-09	Compositions for the freeze protection of coal solids
JPS60155787A (ja)	1985-08-15	粉末着色剤による染色方法とこれに用いる着色剤組成物
US20020106391A1 (en)	2002-08-08	Process for making antimicrobial agents in aqueous dispersion form containing 2-(4- thiazolyl)-benzimidazole alone or in combination with 1,2-dibromo-2,4-dicyanobutane
US4775416A (en)	1988-10-04	Timber branding
EP0549865B1 (de)	1998-07-01	Verfahren zur Herstellung von Trockenstoffen für flüssige Beschichtungsstoffe, Trockenstoffe und deren Verwendung
DE3834875A1 (de)	1990-04-19	Staubfreie zusammensetzungen
EP0186458A1 (de)	1986-07-02	Markieren von Holz
SU1556683A1 (ru)	1990-04-15	Состав дл дезинфекции
KR20000077166A (ko)	2000-12-26	안료 조성물의 제조 방법
US3931341A (en)	1976-01-06	Treated pentachlorophenol
US1965508A (en)	1934-07-03	Method of treating wood for protecting the same from bluing