RU96107237A - TONERS FOR POLYESTERS - Google Patents
TONERS FOR POLYESTERSInfo
- Publication number
- RU96107237A RU96107237A RU96107237/04A RU96107237A RU96107237A RU 96107237 A RU96107237 A RU 96107237A RU 96107237/04 A RU96107237/04 A RU 96107237/04A RU 96107237 A RU96107237 A RU 96107237A RU 96107237 A RU96107237 A RU 96107237A
- Authority
- RU
- Russia
- Prior art keywords
- alkyl
- alkylene
- substituted
- group
- hydrogen
- Prior art date
Links
- 229920000728 polyester Polymers 0.000 title claims 16
- 229910052739 hydrogen Inorganic materials 0.000 claims 32
- 239000001257 hydrogen Substances 0.000 claims 32
- 150000002431 hydrogen Chemical class 0.000 claims 23
- 125000003118 aryl group Chemical group 0.000 claims 17
- 150000001875 compounds Chemical class 0.000 claims 16
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 15
- 229910052736 halogen Inorganic materials 0.000 claims 15
- 150000002367 halogens Chemical class 0.000 claims 15
- -1 C 1 - C 6 -alkyl Chemical class 0.000 claims 8
- 125000002947 alkylene group Chemical group 0.000 claims 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 8
- RZVHIXYEVGDQDX-UHFFFAOYSA-N Anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 6
- 239000004721 Polyphenylene oxide Substances 0.000 claims 5
- 229920000570 polyether Polymers 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 3
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000005239 aroylamino group Chemical group 0.000 claims 3
- 125000004657 aryl sulfonyl amino group Chemical group 0.000 claims 3
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims 3
- 125000005110 aryl thio group Chemical group 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000005647 linker group Chemical group 0.000 claims 3
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 2
- 125000000732 arylene group Chemical group 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 125000001246 bromo group Chemical group Br* 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- XBNVWXKPFORCRI-UHFFFAOYSA-N 2H-naphtho[2,3-f]quinolin-1-one Chemical compound C1=CC=CC2=CC3=C4C(=O)CC=NC4=CC=C3C=C21 XBNVWXKPFORCRI-UHFFFAOYSA-N 0.000 claims 1
- 125000005236 alkanoylamino group Chemical group 0.000 claims 1
- 230000002708 enhancing Effects 0.000 claims 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 1
Claims (1)
###1
в которой R выбирают из группы, содержащей водород, C1 - C6-алкил, галоген, карбокси и C1 - C6 R1 и R2 независимо друг от друга представляют собой C1 - C6-алкил; R3 выбирают из группы, содержащей водород, галоген, C1 - C6-алкил, замещенный C1 - C6-алкил, гидрокси, C1 - C6-алкокси, замещенный C1 - C6-алкокси, циано, тиоциано, C1 - C6-алкилтио, замещенный C1 - C6-алкилтио, C1 - C6-алкилсульфонил, замещенный C1 - C6-алкилсульфонил, C1 - C6-алкоксикарбонил, карбокси, арилокси, арилтио, арилсульфонил и SO2N(R4)R5X, если m и/или n = 0; R4 выбирают из группы, содержащей водород, C1 - C6-алкил, замещенный C1 - C6-алкил, C3 - C8-алкенил, C3 - C8-алкинил, C3 - C7-циклоалкил и арил; R5 - связывающая группа, выбранная из группы, содержащей C3 - C8-алкилен, C1 - C6-алкилен-Z-C1 - C6-алкилен, арилен-C1 - C6 - алкилен, арилен-Z-C1 - C6-алкилен, C3 - C7-циклоалкилен, C1 - C6 - алкилен-циклоалкилен-C1 - C6-алкилен, C1 - C6-алкилен-арилен-C1 - C6-алкилен и C1 - C6 - алкилен-Z-арилен-Z-C1 - C6 - алкилен, где Z выбирают из -O-, -S- или SO2; X представляет собой галоген или реактивную полиэфирную группу; и m и n независимо друг от друга представляют собой 0 или 1; при условии, что присутствует по меньшей мере одна полиэфирная реактивная группа; вместе с по крайней мере одним красным соединением антрахинона или антрапиридона, выбранным из группы соединений, имеющих приведенные ниже формулы (II)-(X):
###2
###3
###4
###5
###6
###7
###8
###9
###10
в которых R6 выбирают из группы, содержащей водород, C1 - C6-алкил, замещенный C1 - C6-алкил, C3 - C7-циклоалкил или арил; R7 представляет собой водород или от одной до трех групп, которые выбирают из C1 - C6-алкила, замещенного C1 - C6-алкила, C1 - C6-алканоиламино, галогена, C1 - C6-алкил-C1 - C6-алкокси, C1 - C6-алкилтио; R8 и R9 одинаковые или разные, выбранные из группы, включающей C1 - C6-алкил, замещенный C1 - C6-алкил, C3 - C7-циклоалкил или арил; R10 выбирают из группы, включающей C1 - C6-алкил, замещенный С1 - C6-алкил, C3 - C7-циклоалкил или арил; R11 выбирают из группы, содержащей водород, C1 - C12-алкил, замещенный C1 - C12-алкил, C3 - C7-циклоалкил и арил; R12 представляет собой водород или от одной до трех групп, которые выбирают из C1 - C6-алкила, замещенного C1 - C6-алкила, C1 - C6-алкокси, замещенного C1 - C6-алкокси, C1 - C6-алкилтио, замещенного C1 - -C6-алкилтио, галогена, гидрокси, C1 - C6-алканоиламино, ароиламино, C1 - C6-алкилсульфониламино и арилсульфониламино; R13 и R14 выбирают из водорода, циано или CO2R10; R15 представляет собой определенные ранее R4 или R5X; L представляет собой -CO- или -SO2; X имеет значения, определенные выше; m = 0 или 1; p = 12 или 2, при условии что R13 представляет собой водород, когда m = 0, и что присутствует по меньшей мере одна реактивная полиэфирная группа.1. Molded polyether or polyester in the form of fibrils, copolymerized in sufficient to enhance the amount of at least one blue compound 1,4-bis (2,6-dialkidanilino) anthraquinone, which is of the formula I:
###one
in which R is selected from the group containing hydrogen, C 1 - C 6 -alkyl, halogen, carboxy and C 1 - C 6 R 1 and R 2 independently of one another represent C 1 - C 6 -alkyl; R 3 selected from the group containing hydrogen, halogen, C 1 - C 6 -alkyl, substituted C 1 - C 6 -alkyl, hydroxy, C 1 - C 6 -alkoxy, substituted C 1 - C 6 -alkoxy, cyano, thiociano , C 1 -C 6 -alkylthio, substituted C 1 -C 6 -alkylthio, C 1 -C 6 -alkylsulfonyl, substituted C 1 -C 6 -alkylsulfonyl, C 1 -C 6 -alkoxycarbonyl, carboxy, aryloxy, arylthio, arylsulfonyl and SO 2 N (R 4 ) R 5 X, if m and / or n = 0; R 4 is selected from the group containing hydrogen, C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 3 -C 8 -alkenyl, C 3 -C 8 -alkynyl, C 3 -C 7 -cycloalkyl and aryl; R 5 is a linking group selected from the group consisting of C 3 - C 8 alkylene, C 1 - C 6 alkylene-ZC 1 - C 6 alkylene, arylene-C 1 - C 6 - alkylene, arylene-ZC 1 - C 6 -alkylene, C 3 - C 7 -cycloalkylene, C 1 - C 6 - alkylene-cycloalkylene-C 1 - C 6 -alkylene, C 1 - C 6 -alkylene-arylene-C 1 - C 6 -alkylene and C 1 - C 6 - alkylene-Z-arylene-ZC 1 - C 6 - alkylene, where Z is selected from -O-, -S- or SO 2 ; X is a halogen or reactive polyether group; and m and n are independently 0 or 1; with the proviso that at least one polyester reactive group is present; together with at least one red anthraquinone or anthrapyridone compound selected from the group of compounds having the formulas (II) - (X) below:
### 2
### 3
###four
###five
### 6
### 7
###eight
###9
###ten
in which R 6 is selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 3 -C 7 -cycloalkyl or aryl; R 7 is hydrogen or from one to three groups selected from C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 1 -C 6 -alkanoylamino, halogen, C 1 -C 6 -alkyl- C 1 - C 6 alkoxy, C 1 - C 6 alkylthio; R 8 and R 9 are the same or different, selected from the group comprising C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 3 -C 7 -cycloalkyl or aryl; R 10 is selected from the group consisting of C 1 -C 6 alkyl, substituted C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl, or aryl; R 11 is selected from the group containing hydrogen, C 1 -C 12 -alkyl, substituted C 1 -C 12 -alkyl, C 3 -C 7 -cycloalkyl and aryl; R 12 represents hydrogen or from one to three groups that are selected from C 1 - C 6 -alkyl, substituted C 1 - C 6 -alkyl, C 1 - C 6 -alkoxy, substituted C 1 - C 6 -alkoxy, C 1 - C 6 -alkylthio, substituted C 1 -C 6 -alkylthio, halogen, hydroxy, C 1 -C 6 -alkanoylamino, aroylamino, C 1 -C 6 -alkylsulfonylamino and arylsulfonylamino; R 13 and R 14 are selected from hydrogen, cyano or CO 2 R 10 ; R 15 is R 4 or R 5 X as previously defined; L represents -CO- or -SO 2 ; X is as defined above; m = 0 or 1; p = 12 or 2, provided that R 13 is hydrogen when m = 0, and that at least one reactive polyester group is present.
###11
###12
6. Полиэфир согласно любого из пунктов с 1 по 5, отличающийся тем, что красное соединение формулы (V) представляет собой:
###13
###14
7. Полиэфир согласно любого из пунктов с 1 по 6, отличающийся тем, что синее соединение формулы (I) представляет собой
###15
и тем, что красное соединение формулы (V) представляет собой
###16
8. Метод сообщения белизны обычно воспринимаемому желтым полиэфиру, причем для улучшения видимой белизны этого полиэфира указанный метод включает сополимеризацию или смешивание указанного полиэфира с достаточным для отмеченной цели количеством по крайней мере одного синего 1,4-бис(2,6-диалкиланилино)антрахинона формулы (I)
###17
в которой: R выбирают из группы, содержащей водород, C1 - C6, галоген, карбокси и R1 и R2 независимо друг от друга представляют собой C1 - C6-алкил; R3 выбирают из группы, содержащей водород, галоген, C1 - C6-алкил, замещенный C1 - C6-алкил, гидрокси, C1 - C6-алкокси, замещенный C1 - C6-алкокси, циано, тиоциано, C1 - C6-алкилтио, замещенный C1 - C6-алкилтио, C1 - C6-алкилсульфонил, замещенный C1 - C6-алкилсульфонил, C1 - C6-алкоксикарбонил, карбокси, арилокси, арилтио, арилсульфонил и SO2N(R4)R5X, если m и/или n = 0; R4 выбирают из группы, содержащей водород, C1 - C6-алкил, замещенный C1 - C6-алкил, C3 - C8-алкенил, C3 - C8-алкинил, C3 - C7-циклоалкил и арил; R5 - связывающая группа, выбранная из группы, содержащей C1 - C8-алкилен, C1 - C6-алкилен-Z-C1 - C6-алкилен, арилен-C1 - C6-алкилен, арилен-Z-C1 - C6-алкилен, C3 - C7-циклоалкилен, C1 - C6-алкилен-циклоалкилен-C1 - C6-алкилен, C1 - C6-алкилен-арилен-C1 - C6-алкилен и C1 - C6-алкилен-Z-арилен-Z-C1 - C6-алкилен, где Z выбирают из -O-, -S- или SO2; X представляет собой галоген или реактивную полиэфирную группу; и m и n независимо друг от друга представляют собой 0 или 1; при условии, что присутствует по меньшей мере одна полиэфирная реактивная группа; вместе с по крайней мере одним красным соединением антрахинона или антрапиридона, имеющих приведенные ниже формулы (II)-(X):
###18
###19
###20
###21
###22
###23
###24
###25
###26
в которых R6 выбирают из группы, содержащей водород, C1 - C6-алкил, замещенный C1 - C6-алкил, C3 - C7-циклоалкил или арил; R7 представляет собой водород или от одной до трех групп, которые выбирают из C1 - C6-алкила, замещенного C1 - C6-алкила, C1 - C6-алканоиламино, галогена, C1 - C6-алкил-C1 - C6-алкокси, C1 - C6-алкилтио; R8 и R9 одинаковые или разные, выбранные из группы, включающей C1 - C6-алкил, замещенный C1 - C6-алкил, C3 - C7-циклоалкил или арил; R10 выбирают из группы, включающей C1 - C6-алкил, C3 - C7-циклоалкил или арил; R11 выбирают из группы, содержащей водород, C1 - C12-алкил, замещенный C1 - C12-алкил, C3 - C7-циклоалкил и арил; R12 представляет собой водород или от одной до трех групп, которые выбирают из C1 - C6-алкила, замещенного C1 - C6-алкила, C1 - C6-алкокси, замещенного C1 - C6-алкокси, C1 - C6-алкилтио, замещенного C1 - C6-алкилтио, C1 - C6-алканоиламино, галогена, ароиламино, C1 - C6-алкилсульфониламино и арилсульфониламино; R13 и R14 выбирают из водорода, циано или CO2R10; R15 представляет собой определенные ранее R4 или R5X; L представляет собой -CO- или -SO2-; X имеет значения, определенные выше; m = 0 или 1; p = 1 или 2, при условии что R13 представляет собой водород, когда m = 0, и что при сополимеризации соединений формул (II)-(X) присутствует по меньшей мере одна реактивная полиэфирная группа.5. Polyester according to claims 1, 2, 3 or 4, characterized in that the compound of formula (I) is:
###eleven
###12
6. The polyester according to any one of paragraphs 1 to 5, characterized in that the red compound of formula (V) is:
###13
###14
7. The polyester according to any one of paragraphs 1 to 6, characterized in that the blue compound of formula (I) is
###15
and in that the red compound of formula (V) is
###sixteen
8. The method of reporting whiteness is usually perceived yellow polyester, and to improve the visible whiteness of this polyester, this method involves copolymerizing or mixing the specified polyester with a sufficient amount for the marked purpose of at least one blue 1,4-bis (2,6-dialkylanilino) anthraquinone of the formula (I)
### 17
in which: R is selected from the group consisting of hydrogen, C 1 - C 6 , halogen, carboxy and R 1 and R 2 independently of one another represent C 1 - C 6 -alkyl; R 3 selected from the group containing hydrogen, halogen, C 1 - C 6 -alkyl, substituted C 1 - C 6 -alkyl, hydroxy, C 1 - C 6 -alkoxy, substituted C 1 - C 6 -alkoxy, cyano, thiociano , C 1 -C 6 -alkylthio, substituted C 1 -C 6 -alkylthio, C 1 -C 6 -alkylsulfonyl, substituted C 1 -C 6 -alkylsulfonyl, C 1 -C 6 -alkoxycarbonyl, carboxy, aryloxy, arylthio, arylsulfonyl and SO 2 N (R 4 ) R 5 X, if m and / or n = 0; R 4 is selected from the group containing hydrogen, C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 3 -C 8 -alkenyl, C 3 -C 8 -alkynyl, C 3 -C 7 -cycloalkyl and aryl; R 5 is a linking group selected from the group consisting of C 1 - C 8 alkylene, C 1 - C 6 alkylene-ZC 1 - C 6 alkylene, arylene-C 1 - C 6 alkylene, arylene-ZC 1 - C 6 -alkylene, C 3 -C 7 -cycloalkylene, C 1 -C 6 -alkylene-cycloalkylene-C 1 -C 6 -alkylene, C 1 -C 6 -alkylene-arylene-C 1 -C 6 -alkylene and C 1 - C 6 -alkylene-Z-arylene-ZC 1 - C 6 -alkylene, where Z is selected from -O-, -S- or SO 2 ; X is a halogen or reactive polyether group; and m and n are independently 0 or 1; with the proviso that at least one polyester reactive group is present; together with at least one red compound of anthraquinone or anthrapyridone, having the formulas (II) - (X) below:
###18
###nineteen
###20
### 21
### 22
### 23
### 24
### 25
### 26
in which R 6 is selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 3 -C 7 -cycloalkyl or aryl; R 7 is hydrogen or from one to three groups selected from C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 1 -C 6 -alkanoylamino, halogen, C 1 -C 6 -alkyl- C 1 - C 6 alkoxy, C 1 - C 6 alkylthio; R 8 and R 9 are the same or different, selected from the group comprising C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 3 -C 7 -cycloalkyl or aryl; R 10 is selected from the group consisting of C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl, or aryl; R 11 is selected from the group containing hydrogen, C 1 -C 12 -alkyl, substituted C 1 -C 12 -alkyl, C 3 -C 7 -cycloalkyl and aryl; R 12 represents hydrogen or from one to three groups that are selected from C 1 - C 6 -alkyl, substituted C 1 - C 6 -alkyl, C 1 - C 6 -alkoxy, substituted C 1 - C 6 -alkoxy, C 1 - C 6 -alkylthio, substituted C 1 -C 6 -alkylthio, C 1 -C 6 -alkanoylamino, halogen, aroylamino, C 1 -C 6 -alkylsulfonylamino and arylsulfonylamino; R 13 and R 14 are selected from hydrogen, cyano or CO 2 R 10 ; R 15 is R 4 or R 5 X as previously defined; L represents -CO- or -SO 2 -; X is as defined above; m = 0 or 1; p = 1 or 2, provided that R 13 is hydrogen, when m = 0, and that at least one reactive polyether group is present when copolymerizing compounds of formulas (II) to (X).
###27
а красное соединение формулы (V) представляет собой
###28
11. Тонирующий состав премикса, содержащий смесь по меньшей мере одного синего соединения 1,4-бис(2,6-диалкиланилино)антрахинона, имеющего формулу (I):
###29
в которой R выбирают из группы, содержащей водород, C1 - C6-алкил, галоген, карбокси и C1 - C6 R1 и R2 независимо друг от друга представляют собой C1 - C6-алкил; R3 выбирают из группы, содержащей водород, галоген, C1 - C6-алкил, замещенный C1 - C6-алкил, гидрокси, C1 - C6-алкокси, замещенный C1 - C6-алкокси, циано, тиоциано, C1 - C6-алкилтио, замещенный C1 - C6-алкилтио, C1 - C6-алкилсульфонил, замещенный C1 - C6-алкилсульфонил, C1 - C6-алкоксикарбонил, карбокси, арилоси, арилтио, арилсульфонил и SO2N(R4)R5X, если m и/или n = 0; R4 выбирают из группы, содержащей водород, C1 - C6-алкил, замещенный C1 - C6-алкил, C3 - C8-алкенил, C3 - C8-алкинил, C3 - C7-циклоалкил и арил; R5 - связывающая группа, выбранная из группы, содержащей C1 - C8-алкилен, C1 - C6-алкилен-Z-C1 - C6-алкилен, арилен-C1 - C6-алкилен, арилен-Z-C1 - C6-алкилен, C3 - C7-циклоалкилен, C1 - C6-алкилен-циклоалкилен-C1 - C6-алкилен, C1 - C6-алкилен-арилен-C1 - C6-алкилен и C1 - C6-алкилен-Z-арилен-Z-C1 - C6-алкилен, где Z выбирают из -O-, -S- или SO2; X представляет собой галоген или реактивную полиэфирную группу; и m и n независимо друг от друга представляют собой 0 или 1; при условии, что присутствует по меньшей мере одна полиэфирная реактивная группа; вместе с по крайней мере одним красным соединением антрахинона или антрапиридона, выбранным из группы соединений, имеющих приведенные ниже формулы (II)-(X):
###30
###31
###32
###33
###34
###35
###36
###37
###38
в которых R6 выбирают из группы, содержащей водород, C1 - C6-алкил, замещенный C1 - C6-алкил, C3 - C7-циклоалкил или арил; R7 представляет собой водород или от одной до трех групп, которые выбирают из C1 - C6-алкила, замещенного C1 - C6-алкила, C1 - C6-алканоиламино, галогена, гидрокси, C1 - C6-алкил-C1 - C6-алкокси, C1 - C6-алкилтио; R8 и R9 одинаковые или разные, выбранные из группы, включающей C1 - C6-алкил, замещенный C1 - C6-алкил, C3 - C7-циклоалкил или арил; R10 выбирают из группы, включающей C1 - C6-алкил, замещенный C1 - C6-алкил, C3 - C7-циклоалкил или арил; R11 выбирают из группы, содержащей водород, C1 - C12-алкил, замещенный C1 - C12-алкил, C3 - C7-циклоалкил и арил; R12 представляет собой водород или от одной до трех групп, которые выбирают из C1 - C6-алкила, замещенного C1 - C6-алкила, C1 - C6-алкокси, замещенного C1 - C6-алкокси, C1 - C6-алкилтио, замещенного C1 - C6-алкилтио, C1 - C6-алканоиламино, галогена, гидрокси, ароиламино, C1 - C6-алкилсульфониламино и арилсульфониламино; R13 и R14 выбирают из водорода, циано или CO2R10; R15 представляет собой определенные ранее R4 или R5X; L представляет собой -CO- или -SO2; X имеет значения, определенные выше; m = 0 или 1; p = 1 или 2, при условии, что R13 представляет собой водород, когда m = 0.10. The method according to claim 8 or 9, in which the blue compound I is:
### 27
and the red compound of formula (V) is
### 28
11. The toning composition of the premix containing a mixture of at least one blue compound 1,4-bis (2,6-dialkylanilino) anthraquinone, having the formula (I):
### 29
in which R is selected from the group containing hydrogen, C 1 - C 6 -alkyl, halogen, carboxy and C 1 - C 6 R 1 and R 2 independently of one another represent C 1 - C 6 -alkyl; R 3 selected from the group containing hydrogen, halogen, C 1 - C 6 -alkyl, substituted C 1 - C 6 -alkyl, hydroxy, C 1 - C 6 -alkoxy, substituted C 1 - C 6 -alkoxy, cyano, thiociano C 1 -C 6 alkylthio, substituted C 1 -C 6 alkylthio, C 1 -C 6 alkylsulfonyl, substituted C 1 -C 6 alkylsulfonyl, C 1 -C 6 alkoxycarbonyl, carboxy, arylsi, arylthio, arylsulfonyl and SO 2 N (R 4 ) R 5 X, if m and / or n = 0; R 4 is selected from the group containing hydrogen, C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 3 -C 8 -alkenyl, C 3 -C 8 -alkynyl, C 3 -C 7 -cycloalkyl and aryl; R 5 is a linking group selected from the group consisting of C 1 - C 8 alkylene, C 1 - C 6 alkylene-ZC 1 - C 6 alkylene, arylene-C 1 - C 6 alkylene, arylene-ZC 1 - C 6 -alkylene, C 3 -C 7 -cycloalkylene, C 1 -C 6 -alkylene-cycloalkylene-C 1 -C 6 -alkylene, C 1 -C 6 -alkylene-arylene-C 1 -C 6 -alkylene and C 1 - C 6 -alkylene-Z-arylene-ZC 1 - C 6 -alkylene, where Z is selected from -O-, -S- or SO 2 ; X is a halogen or reactive polyether group; and m and n are independently 0 or 1; with the proviso that at least one polyester reactive group is present; together with at least one red anthraquinone or anthrapyridone compound selected from the group of compounds having the formulas (II) - (X) below:
###thirty
### 31
### 32
### 33
### 34
### 35
### 36
### 37
### 38
in which R 6 is selected from the group consisting of hydrogen, C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 3 -C 7 -cycloalkyl or aryl; R 7 is hydrogen or from one to three groups selected from C 1 - C 6 alkyl, substituted C 1 - C 6 alkyl, C 1 - C 6 alkanoylamino, halogen, hydroxy, C 1 - C 6 - alkyl-C 1 -C 6 -alkoxy, C 1 -C 6 -alkylthio; R 8 and R 9 are the same or different, selected from the group comprising C 1 -C 6 -alkyl, substituted C 1 -C 6 -alkyl, C 3 -C 7 -cycloalkyl or aryl; R 10 is selected from the group consisting of C 1 -C 6 alkyl, substituted C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl or aryl; R 11 is selected from the group containing hydrogen, C 1 -C 12 -alkyl, substituted C 1 -C 12 -alkyl, C 3 -C 7 -cycloalkyl and aryl; R 12 represents hydrogen or from one to three groups that are selected from C 1 - C 6 -alkyl, substituted C 1 - C 6 -alkyl, C 1 - C 6 -alkoxy, substituted C 1 - C 6 -alkoxy, C 1 - C 6 -alkylthio, substituted C 1 -C 6 -alkylthio, C 1 -C 6 -alkanoylamino, halogen, hydroxy, aroylamino, C 1 -C 6 -alkylsulfonylamino and arylsulfonylamino; R 13 and R 14 are selected from hydrogen, cyano or CO 2 R 10 ; R 15 is R 4 or R 5 X as previously defined; L represents -CO- or -SO 2 ; X is as defined above; m = 0 or 1; p = 1 or 2, provided that R 13 is hydrogen when m = 0.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US116,419 | 1993-09-03 | ||
US08/116,419 US5372864A (en) | 1993-09-03 | 1993-09-03 | Toners for polyesters |
PCT/US1994/009294 WO1995006677A1 (en) | 1993-09-03 | 1994-08-17 | Toners for polyesters |
Publications (2)
Publication Number | Publication Date |
---|---|
RU96107237A true RU96107237A (en) | 1998-07-20 |
RU2142477C1 RU2142477C1 (en) | 1999-12-10 |
Family
ID=22367085
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU96107237/04A RU2142477C1 (en) | 1993-09-03 | 1994-08-17 | Polyester, method of imparting whiteness to polyesters, tonic composition of premix, molded product |
Country Status (19)
Country | Link |
---|---|
US (2) | US5372864A (en) |
EP (1) | EP0716666B1 (en) |
JP (1) | JP3055698B2 (en) |
KR (1) | KR100335545B1 (en) |
CN (1) | CN1052738C (en) |
AT (1) | ATE166081T1 (en) |
AU (1) | AU680292B2 (en) |
BR (1) | BR9407453A (en) |
CA (1) | CA2170145C (en) |
CO (1) | CO4410419A1 (en) |
CZ (1) | CZ61396A3 (en) |
DE (1) | DE69410277T2 (en) |
ES (1) | ES2115971T3 (en) |
HU (1) | HU214928B (en) |
MY (1) | MY111530A (en) |
NZ (1) | NZ273139A (en) |
PL (1) | PL309635A1 (en) |
RU (1) | RU2142477C1 (en) |
WO (1) | WO1995006677A1 (en) |
Families Citing this family (149)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6495656B1 (en) | 1990-11-30 | 2002-12-17 | Eastman Chemical Company | Copolyesters and fibrous materials formed therefrom |
JP2000511211A (en) * | 1995-11-13 | 2000-08-29 | イーストマン ケミカル カンパニー | Thermostable polyesters produced using antimony compounds as catalysts |
US5608031A (en) * | 1995-11-30 | 1997-03-04 | Eastman Chemical Company | Polyesters modified with 1,4-cyclohexaned imethanol having high clarity prepared utilizing an antimony containing catalyst/stabilizer system |
DE69736354T2 (en) * | 1996-09-11 | 2006-11-16 | Nippon Kayaku K.K. | ANTHRAPYRIDONE COMPOUNDS, AQUEOUS INK COMPOSITION, AND ITEMS PAINTED THEREFOR |
US5962557A (en) * | 1996-09-30 | 1999-10-05 | Eastman Chemical Corporation | Polyesters containing copolymerized substituted 1,4-bis(2,6-dialkylanilino)-9, 10-anthraquinones as colorants |
CN1245516A (en) * | 1996-11-27 | 2000-02-23 | 伊斯曼化学公司 | Method for preparing light-absorbing polymeric compositions |
US5859116A (en) * | 1997-01-21 | 1999-01-12 | Eastman Chemical Company | Clarity and adjustable shrinkage of shrink films using miscible polyester blends |
US5688899A (en) * | 1997-01-21 | 1997-11-18 | Eastman Chemical Company | Clarity copolyester |
US5716769A (en) * | 1997-03-07 | 1998-02-10 | Eastman Kodak Company | Elements containing blue tinted hydrophilic colloid layers |
US6270945B1 (en) * | 1997-03-19 | 2001-08-07 | Kodak Polychrome Graphics, Llc | Photosensitive compositions and elements comprising dyed photosensitive polyesters |
US5744294A (en) * | 1997-04-30 | 1998-04-28 | Eastman Kodak Company | Radiographic element modified to provide protection from visual fatigue |
US5851243A (en) * | 1997-04-30 | 1998-12-22 | Eastman Kodak Company | Radiographic elements capable of rapid access processing modified to reduce red light transmission |
DE69802745T2 (en) * | 1997-06-05 | 2002-09-12 | DAINICHISEIKA COLOR & CHEMICALS MFG. CO., LTD. | Manufacturing method of a composition of colored small particles and a composition of colored small particles produced by the method |
DE69836223T2 (en) * | 1997-08-28 | 2007-08-30 | Eastman Chemical Co., Kingsport | IMPROVED COPOLYMER BINDER FIBERS |
US6231976B1 (en) | 1997-08-28 | 2001-05-15 | Eastman Chemical Company | Copolyester binder fibers |
DE69817212T2 (en) * | 1997-11-06 | 2004-06-24 | Eastman Chemical Co., Kingsport | COPOLYESTER-BINDER FIBERS |
KR100580937B1 (en) * | 1998-03-25 | 2006-05-17 | 니폰 카야쿠 가부시키가이샤 | Novel anthrapyridone compounds, water-based magenta ink composition, and method of ink-jet recording |
WO2001010929A1 (en) | 1999-08-06 | 2001-02-15 | Eastman Chemical Company | Polyesters having a controlled melting point and fibers formed therefrom |
US6362306B1 (en) * | 1999-08-17 | 2002-03-26 | Eastman Chemical Company | Reactor grade copolyesters for shrink film applications |
WO2001014452A1 (en) * | 1999-08-24 | 2001-03-01 | Eastman Chemical Company | Preparation of polyesters employing antimony catalysts and acidic phosphorus compounds |
US6384180B1 (en) | 1999-08-24 | 2002-05-07 | Eastman Chemical Company | Method for making polyesters employing acidic phosphorus-containing compounds |
ES2207288T3 (en) * | 1999-08-24 | 2004-05-16 | Eastman Chemical Company | METHOD FOR PRODUCING POLYESTERS USING COMPOUNDS CONTAINING ACID PHOSPHORUS |
US6727372B2 (en) | 2000-08-07 | 2004-04-27 | Eastman Chemical Company | Colorant compounds containing copolymerizable vinyl groups |
CN1234778C (en) * | 2000-08-07 | 2006-01-04 | 伊斯曼化学公司 | Thermally stable, anthraquinone colorants contg. copolymerizable vinyl groups |
US6620858B2 (en) | 2000-08-07 | 2003-09-16 | Eastman Chemical Company | Colorants containing copolymerizable vinyl groups and sulfonamide linkages |
JP2004506061A (en) | 2000-08-07 | 2004-02-26 | イーストマン ケミカル カンパニー | Thermally stable anthraquinone colorant containing copolymerizable vinyl groups |
US20020082360A1 (en) * | 2000-11-03 | 2002-06-27 | Conn Roy Lee | Films and articles formed from blends of polycarbonate and polyester |
US6569957B2 (en) | 2000-11-03 | 2003-05-27 | Eastman Chemical Company | Blends of polycarbonate and polyester and sheets and films formed therefrom |
US7513947B2 (en) * | 2000-11-13 | 2009-04-07 | Ei Du Pont De Nemours And Company | Colored thermoplastic resin compositions for laser welding, specific neutral anthraquinone dyes as colorants therefor, and molded product therefrom |
US6429278B1 (en) | 2001-01-22 | 2002-08-06 | Eastman Chemical Company | Process for manufacture of polyesters based on 1,4-cyclohexanedimethanol and isophthalic acid |
US6489433B2 (en) | 2001-02-23 | 2002-12-03 | E. I. Du Pont De Nemours And Company | Metal-containing composition and process therewith |
US20070032598A1 (en) * | 2001-07-24 | 2007-02-08 | Cyr Michael J | Thermally stable, anthraquinone colorants containing copolymerizable vinyl groups |
US6713641B2 (en) * | 2001-10-19 | 2004-03-30 | Eastman Chemical Company | Reactive anthraquinone colorant compounds and polymeric materials reacted therewith |
US6641920B2 (en) | 2002-02-08 | 2003-11-04 | Eastman Chemical Company | Ultraviolet protected multi-layer structures of copolyester/polycarbonate blends |
US6723768B2 (en) | 2002-03-27 | 2004-04-20 | Eastman Chemical Company | Polyester/polycarbonate blends with reduced yellowness |
US6835333B2 (en) * | 2002-05-07 | 2004-12-28 | Milliken & Company | Combinations for use as toners in polyesters |
US6875811B2 (en) | 2002-05-07 | 2005-04-05 | Milliken & Company | Single compound toners for use in polyesters |
US6914120B2 (en) * | 2002-11-13 | 2005-07-05 | Eastman Chemical Company | Method for making isosorbide containing polyesters |
JP4563998B2 (en) * | 2003-03-18 | 2010-10-20 | チバ ホールディング インコーポレーテッド | Colored polymeric articles having a high melting temperature |
US20050054757A1 (en) * | 2003-09-10 | 2005-03-10 | Pearson Jason Clay | Method for reducing the acetaldehyde level in polyesters |
US20050065247A1 (en) * | 2003-09-19 | 2005-03-24 | Carico Douglas Weldon | Liquid coating compositions having improved whiteness |
CA2547351A1 (en) | 2003-12-01 | 2005-07-07 | Dade Behring Marburg Gmbh | Homogeneous detection method |
US7358322B2 (en) * | 2004-03-09 | 2008-04-15 | Eastman Chemical Company | High IV melt phase polyester polymer catalyzed with antimony containing compounds |
US7368523B2 (en) | 2004-11-12 | 2008-05-06 | Eastman Chemical Company | Polyester polymer and copolymer compositions containing titanium nitride particles |
US7541407B2 (en) * | 2004-05-27 | 2009-06-02 | Eastman Chemical Company | Process for adding methine UV light absorbers to PET prepared by direct esterification |
US20050267283A1 (en) * | 2004-05-27 | 2005-12-01 | Weaver Max A | Process for adding nitrogen containing methine light absorbers to poly(ethylene terephthalate) |
US7622580B2 (en) * | 2004-08-13 | 2009-11-24 | Xerox Corporation | Colorant compounds |
JP5336737B2 (en) | 2004-08-17 | 2013-11-06 | インヴィスタ テクノロジーズ エスアエルエル | Colored oxygen scavenging polymer |
US20060047102A1 (en) | 2004-09-02 | 2006-03-02 | Stephen Weinhold | Spheroidal polyester polymer particles |
US7662880B2 (en) | 2004-09-03 | 2010-02-16 | Eastman Chemical Company | Polyester polymer and copolymer compositions containing metallic nickel particles |
US20060051542A1 (en) * | 2004-09-03 | 2006-03-09 | Zhiyong Xia | Polyester polymer and copolymer compositions containing metallic molybdenum particles |
US7300967B2 (en) * | 2004-11-12 | 2007-11-27 | Eastman Chemical Company | Polyester polymer and copolymer compositions containing metallic titanium particles |
US20060105129A1 (en) * | 2004-11-12 | 2006-05-18 | Zhiyong Xia | Polyester polymer and copolymer compositions containing titanium carbide particles |
US7262476B2 (en) * | 2004-11-30 | 2007-08-28 | Agere Systems Inc. | Semiconductor device having improved power density |
US20060122300A1 (en) * | 2004-12-07 | 2006-06-08 | Zhiyong Xia | Polyester polymer and copolymer compositions containing steel particles |
US20060177614A1 (en) * | 2005-02-09 | 2006-08-10 | Zhiyong Xia | Polyester polymer and copolymer compositions containing metallic tantalum particles |
US7576171B2 (en) | 2005-06-17 | 2009-08-18 | Eastman Chemical Company | Pacifiers comprising polyester compositions formed from 2,2,4,4-tetramethyl-1,3-cyclobutanediol and 1,4-cyclohexanedimethanol |
US20060222795A1 (en) * | 2005-03-31 | 2006-10-05 | Howell Earl E Jr | Polyester polymer and copolymer compositions containing particles of one or more transition metal compounds |
CN1313512C (en) * | 2005-05-17 | 2007-05-02 | 薛纪良 | Process of preparing polyester slices for high transparent energy saving film |
US20060270806A1 (en) * | 2005-05-26 | 2006-11-30 | Hale Wesley R | Miscible high Tg polyester/polymer blend compositions and films formed therefrom |
US20060270773A1 (en) * | 2005-05-26 | 2006-11-30 | Hale Wesley R | Polyester-polycarbonate blends for diffuser sheets with improved luminance |
US20060287471A1 (en) * | 2005-06-16 | 2006-12-21 | Schreiber Benjamin R | Accelerated acetaldehyde testing of polymers |
US8557950B2 (en) | 2005-06-16 | 2013-10-15 | Grupo Petrotemex, S.A. De C.V. | High intrinsic viscosity melt phase polyester polymers with acceptable acetaldehyde generation rates |
US20100298523A1 (en) * | 2005-06-17 | 2010-11-25 | Eastman Chemical Company | Polyester Compositions Which Comprise Cyclobutanediol and at Least One Phosphorus Compound |
US7704605B2 (en) | 2006-03-28 | 2010-04-27 | Eastman Chemical Company | Thermoplastic articles comprising cyclobutanediol having a decorative material embedded therein |
US20110144266A1 (en) * | 2005-06-17 | 2011-06-16 | Eastman Chemical Company | Thermoplastic Articles Comprising Cyclobutanediol Having a Decorative Material Embedded Therein |
US7776942B2 (en) | 2005-09-16 | 2010-08-17 | Eastman Chemical Company | Polyester polymer and copolymer compositions containing particles of titanium nitride and carbon-coated iron |
US7745512B2 (en) | 2005-09-16 | 2010-06-29 | Eastman Chemical Company | Polyester polymer and copolymer compositions containing carbon-coated iron particles |
US7932345B2 (en) | 2005-09-16 | 2011-04-26 | Grupo Petrotemex, S.A. De C.V. | Aluminum containing polyester polymers having low acetaldehyde generation rates |
US9267007B2 (en) | 2005-09-16 | 2016-02-23 | Grupo Petrotemex, S.A. De C.V. | Method for addition of additives into a polymer melt |
US8431202B2 (en) | 2005-09-16 | 2013-04-30 | Grupo Petrotemex, S.A. De C.V. | Aluminum/alkaline or alkali/titanium containing polyesters having improved reheat, color and clarity |
US7655746B2 (en) | 2005-09-16 | 2010-02-02 | Eastman Chemical Company | Phosphorus containing compounds for reducing acetaldehyde in polyesters polymers |
US7838596B2 (en) | 2005-09-16 | 2010-11-23 | Eastman Chemical Company | Late addition to effect compositional modifications in condensation polymers |
US20070100125A1 (en) * | 2005-10-28 | 2007-05-03 | Crawford Emmett D | Polyester compositions comprising minimal amounts of cyclobutanediol |
US20100096589A1 (en) * | 2005-10-28 | 2010-04-22 | Emmett Dudley Crawford | Polyester compositions containing low amounts of cyclobutanediol and articles made therefrom |
US20070106054A1 (en) * | 2005-10-28 | 2007-05-10 | Crawford Emmett D | Polyester compositions containing cyclobutanediol having a certain combination of inherent viscosity and high glass transition temperature and articles made therefrom |
ATE505500T1 (en) * | 2005-10-28 | 2011-04-15 | Eastman Chem Co | HIGH GLASS TRANSITION TEMPERATURE POLYESTER COMPOSITIONS CONTAINING CYCLOBUTANEDIOL AND ARTICLES MADE THEREFROM |
US20070100122A1 (en) * | 2005-10-28 | 2007-05-03 | Crawford Emmett D | Polyester compositions containing cyclobutanediol and articles made therefrom |
US8193302B2 (en) | 2005-10-28 | 2012-06-05 | Eastman Chemical Company | Polyester compositions which comprise cyclobutanediol and certain phosphate thermal stabilizers, and/or reaction products thereof |
DE602006009691D1 (en) * | 2005-10-28 | 2009-11-19 | Eastman Chem Co | MADE OF 2,2,4,4-TETRAMETHYL-1,3-CYCLOBUTANDIOL AND 1,4-CYCLOHEXANDIMETHANOL MIXED POLYESTER COMPOSITIONS COMPREHENSIVE RESTAURANT GLASS |
US20100087574A1 (en) * | 2005-10-28 | 2010-04-08 | Emmett Dudley Crawford | Polyester compositions containing cyclobutanediol having a certain combination of inherent viscosity and moderate glass transition temperature and articles made therefrom |
US9598533B2 (en) | 2005-11-22 | 2017-03-21 | Eastman Chemical Company | Polyester compositions containing cyclobutanediol having a certain combination of inherent viscosity and moderate glass transition temperature and articles made therefrom |
US7737246B2 (en) | 2005-12-15 | 2010-06-15 | Eastman Chemical Company | Polyester compositions which comprise cyclobutanediol, cyclohexanedimethanol, and ethylene glycol and manufacturing processes therefor |
US20070142511A1 (en) * | 2005-12-15 | 2007-06-21 | Crawford Emmett D | Polyester compositions which comprise cyclobutanediol ethylene glycol, titanium, and phosphorus with improved color and manufacturing processes therefor |
US20070232778A1 (en) * | 2006-03-28 | 2007-10-04 | Leslie Shane Moody | Certain polyester compositions which comprise cyclobutanediol, cyclohexanedimethanol, and high trans-cyclohexanedicarboxylic acid |
US20070232779A1 (en) * | 2006-03-28 | 2007-10-04 | Leslie Shane Moody | Certain polyester compositions which comprise cyclohexanedimethanol, moderate cyclobutanediol, cyclohexanedimethanol, and high trans cyclohexanedicarboxylic acid |
US20100300918A1 (en) * | 2006-03-28 | 2010-12-02 | Eastman Chemical Company | Bottles comprising polyester compositions which comprise cyclobutanediol |
US9169388B2 (en) | 2006-03-28 | 2015-10-27 | Eastman Chemical Company | Polyester compositions which comprise cyclobutanediol and certain thermal stabilizers, and/or reaction products thereof |
US20070260002A1 (en) * | 2006-05-04 | 2007-11-08 | Zhiyong Xia | Titanium nitride particles, methods of making them, and their use in polyester compositions |
US7709593B2 (en) | 2006-07-28 | 2010-05-04 | Eastman Chemical Company | Multiple feeds of catalyst metals to a polyester production process |
US20080027207A1 (en) * | 2006-07-28 | 2008-01-31 | Jason Christopher Jenkins | Non-precipitating alkali/alkaline earth metal and aluminum compositions made with mono-ol ether solvents |
US7709595B2 (en) | 2006-07-28 | 2010-05-04 | Eastman Chemical Company | Non-precipitating alkali/alkaline earth metal and aluminum solutions made with polyhydroxyl ether solvents |
US7745368B2 (en) | 2006-07-28 | 2010-06-29 | Eastman Chemical Company | Non-precipitating alkali/alkaline earth metal and aluminum compositions made with organic hydroxyacids |
US20080058495A1 (en) * | 2006-09-05 | 2008-03-06 | Donna Rice Quillen | Polyester polymer and copolymer compositions containing titanium and yellow colorants |
US20080085390A1 (en) * | 2006-10-04 | 2008-04-10 | Ryan Thomas Neill | Encapsulation of electrically energized articles |
US8563677B2 (en) | 2006-12-08 | 2013-10-22 | Grupo Petrotemex, S.A. De C.V. | Non-precipitating alkali/alkaline earth metal and aluminum solutions made with diols having at least two primary hydroxyl groups |
US20080255280A1 (en) * | 2007-04-11 | 2008-10-16 | Susan Sims | Oxygen-scavenging polymer blends suitable for use in packaging |
US8207289B2 (en) * | 2007-05-23 | 2012-06-26 | Grupo Petrotemex, S.A. De C.V. | High molecular weight polyester polymers with reduced acetaldehyde |
EP2225084B1 (en) | 2007-11-21 | 2013-05-29 | Eastman Chemical Company | Plastic baby bottles, other blow molded articles, and processes for their manufacture |
US8501287B2 (en) | 2007-11-21 | 2013-08-06 | Eastman Chemical Company | Plastic baby bottles, other blow molded articles, and processes for their manufacture |
US8604139B2 (en) * | 2008-01-14 | 2013-12-10 | Eastman Chemical Company | Extrusion profile articles |
US8198371B2 (en) | 2008-06-27 | 2012-06-12 | Eastman Chemical Company | Blends of polyesters and ABS copolymers |
DE102008044487A1 (en) | 2008-08-29 | 2010-03-04 | Lurgi Zimmer Gmbh | Process for the preparation of polymers with neutral color |
US20100159176A1 (en) * | 2008-12-18 | 2010-06-24 | Eastman Chemical Company | Miscible blends of terephthalate polyesters containing 1,4-cyclohexanedimethanol and 2,2,4,4-tetramethylcyclobutane-1,3-diol |
US8895654B2 (en) | 2008-12-18 | 2014-11-25 | Eastman Chemical Company | Polyester compositions which comprise spiro-glycol, cyclohexanedimethanol, and terephthalic acid |
TWI473832B (en) | 2009-03-13 | 2015-02-21 | Saudi Basic Ind Corp | Process for making polyethylene terephthalate |
EP2287225A1 (en) | 2009-08-20 | 2011-02-23 | Saudi Basic Industries Corporation | Process for making polyethylene terephthalate |
US8420868B2 (en) | 2010-12-09 | 2013-04-16 | Eastman Chemical Company | Process for the preparation of 2,2,4,4-tetraalkylcyclobutane-1,3-diols |
US8394997B2 (en) | 2010-12-09 | 2013-03-12 | Eastman Chemical Company | Process for the isomerization of 2,2,4,4-tetraalkylcyclobutane-1,3-diols |
US8420869B2 (en) | 2010-12-09 | 2013-04-16 | Eastman Chemical Company | Process for the preparation of 2,2,4,4-tetraalkylcyclobutane-1,3-diols |
US8633262B2 (en) | 2011-01-17 | 2014-01-21 | Eastman Chemical Company | Haze reduction for blends of aromatic-aliphatic polyesters with aliphatic polyesters and antimicrobial additives |
US20130029068A1 (en) | 2011-07-28 | 2013-01-31 | Eastman Chemical Company | Extrusion blow molded articles |
EP2744834B1 (en) | 2011-08-24 | 2014-12-24 | Lambson Limited | Polymers comprising photoinitiator moieties and dye moieties |
US8906587B2 (en) | 2011-11-02 | 2014-12-09 | Canon Kabushiki Kaisha | Colored resin powder and toner using the colored resin powder |
US20130217830A1 (en) | 2012-02-16 | 2013-08-22 | Eastman Chemical Company | Clear Semi-Crystalline Articles with Improved Heat Resistance |
CN104540837A (en) | 2012-06-28 | 2015-04-22 | 沙特基础工业公司 | Novel titanium catalyst end process for the preparation thereof |
CN103289435B (en) * | 2013-03-04 | 2015-09-02 | 连云港市添立润化工有限公司 | A kind of liquid crystal display pigment derivative and manufacture method thereof |
US9517584B2 (en) | 2013-12-18 | 2016-12-13 | Eastman Chemical Company | Articles comprising isosorbide and processes for their manufacture |
WO2018035341A1 (en) | 2016-08-18 | 2018-02-22 | Eastman Chemical Company | Polyester compositions which comprise tetramethylcyclobutanediol and ethylene glycol for calendering |
WO2018035337A1 (en) | 2016-08-18 | 2018-02-22 | Eastman Chemical Company | Polyester compositions which comprise tetramethylcyclobutandiol and ethylene glycol, with improved catalyst system |
EP3878888A1 (en) | 2016-08-18 | 2021-09-15 | Eastman Chemical Company | Polyester compositions which comprise tetramethyl cyclobutanediol and ethylene glycol, with improved catalyst system |
WO2019089535A2 (en) | 2017-10-30 | 2019-05-09 | Eastman Chemical Company | Low density void containing films |
US10543656B2 (en) | 2018-01-11 | 2020-01-28 | Eastman Chemical Company | Tough shrinkable films |
KR20210070360A (en) | 2018-10-08 | 2021-06-14 | 이스트만 케미칼 컴파니 | Crystallizable Shrinkable Films and Thermoformable Sheets Made from Reactor Grade Resins |
KR20210072065A (en) | 2018-10-08 | 2021-06-16 | 이스트만 케미칼 컴파니 | Crystallizable Shrinkable Films and Thermoformable Sheets Made from Resin Blends |
CN113795367A (en) | 2019-05-10 | 2021-12-14 | 伊士曼化工公司 | Renewable extrusion blow molded articles from blends of copolyesters and recycled PET |
KR20220007657A (en) | 2019-05-10 | 2022-01-18 | 이스트만 케미칼 컴파니 | Recyclable Molded Articles from Blends of Copolyester and Recycled PET |
EP4041797A1 (en) | 2019-10-08 | 2022-08-17 | Eastman Chemical Company | Catalyst systems for crystallizable reactor grade resins with recycled content |
US20220372216A1 (en) | 2019-10-08 | 2022-11-24 | Eastman Chemical Company | Catalyst systems for crystallizable reactor grade resins |
JP2022553090A (en) | 2019-10-25 | 2022-12-21 | イーストマン ケミカル カンパニー | Crystallizable Shrinkable Films and Thermoformable Films and Sheets Made from Reactor Grade Resins with Recycles |
KR20210071535A (en) * | 2019-12-06 | 2021-06-16 | (주)경인양행 | Dye compounds and the use thereof |
EP4132991A1 (en) | 2020-04-06 | 2023-02-15 | Eastman Chemical Company | Crystallizable shrinkable films and thermoformable sheets made from resin blends |
EP4135981A1 (en) | 2020-04-13 | 2023-02-22 | Eastman Chemical Company | Hot-fillable articles made from multilayered thermoformable film and sheet |
US20230331907A1 (en) | 2020-10-08 | 2023-10-19 | Eastman Chemical Company | Shrinkable polyester films |
EP4263665A1 (en) | 2020-12-18 | 2023-10-25 | Eastman Chemical Company | Polyester compositions comprising tetramethyl cyclobutanediol and 1,4-cyclohexanedimethanol having an improved catalyst system comprising titanium and zinc |
WO2023023446A1 (en) | 2021-08-19 | 2023-02-23 | Solutia Inc. | High molecular weight polyesteramides |
TW202315906A (en) | 2021-10-08 | 2023-04-16 | 美商伊士曼化學公司 | Shrinkable polyester films with reduced shrinkage |
WO2023076200A1 (en) | 2021-10-25 | 2023-05-04 | Eastman Chemical Company | Low temperature processes for recycling poly(ethylene terephthalate) |
WO2023091539A1 (en) | 2021-11-22 | 2023-05-25 | Eastman Chemical Company | Recyclable copolyesters articles with living hinges |
CN118284642A (en) | 2021-11-22 | 2024-07-02 | 伊士曼化工公司 | Method of making recyclable copolyester articles with living hinges |
WO2023091544A1 (en) | 2021-11-22 | 2023-05-25 | Eastman Chemical Company | Process for making recyclable copolyesters articles with living hinges |
CN118284564A (en) | 2021-11-22 | 2024-07-02 | 伊士曼化工公司 | Recyclable copolyester article with living hinge |
CN118434789A (en) | 2021-12-16 | 2024-08-02 | 伊士曼化工公司 | Polyester compositions comprising cyclohexanedimethanol or 2, 4-tetramethyl-1, 3-cyclobutanediol and improved catalyst systems therefor |
WO2023178221A1 (en) | 2022-03-18 | 2023-09-21 | Eastman Chemical Company | Multilayer crystallizable shrinkable film and sheet |
WO2023196829A1 (en) | 2022-04-06 | 2023-10-12 | Eastman Chemical Company | Multilayer shrinkable polyester films with improved toughness |
WO2023244956A1 (en) | 2022-06-13 | 2023-12-21 | Eastman Chemical Company | Copolyester compositions having low coefficient of friction |
WO2023244953A1 (en) | 2022-06-13 | 2023-12-21 | Eastman Chemical Company | Copolyesters compositions having low coefficient of friction |
WO2024054767A1 (en) | 2022-09-06 | 2024-03-14 | Eastman Chemical Company | Copolyester blow molded articles with a transparent view stripe |
WO2024092080A1 (en) | 2022-10-28 | 2024-05-02 | Eastman Chemical Company | Recycleable hot melt adhesive copolyester compositions |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE935987C (en) * | 1951-10-18 | 1955-12-01 | Sandoz Ag | Process for the preparation of sulfonic acid amides of the anthraquinone series |
BR6787718D0 (en) * | 1966-06-29 | 1973-06-07 | Eastman Kodak Co | LIGHT SENSITIVE PHOTOGRAPHIC ELEMENT |
JPS5443014B2 (en) * | 1971-09-09 | 1979-12-18 | ||
JPS4910017A (en) * | 1972-05-24 | 1974-01-29 | ||
US4267306A (en) * | 1979-02-15 | 1981-05-12 | Eastman Kodak Company | Polyester polymers containing residues of anthroquinone dyes |
US4420581A (en) * | 1979-03-19 | 1983-12-13 | Eastman Kodak Company | Thermoplastic polyester molding compositions |
US4359570A (en) * | 1980-05-08 | 1982-11-16 | Eastman Kodak Company | Colored polyester containing copolymerized dyes as colorants |
US4403092A (en) * | 1982-11-22 | 1983-09-06 | Eastman Kodak Company | Polyesters containing copolymerized, anthraquinone colorant compounds containing sulfonamido groups |
US4740581A (en) * | 1987-02-24 | 1988-04-26 | Eastman Kodak Company | Condensation copolymers containing copolymerized isoquinoline derivative colorants and products therefrom |
US4745174A (en) * | 1987-04-23 | 1988-05-17 | Eastman Kodak Company | Polyesters having improved whiteness |
US4999418A (en) * | 1989-08-31 | 1991-03-12 | Eastman Kodak Company | Polyesters colored with the residue of heat stable anthraquinone compounds |
-
1993
- 1993-09-03 US US08/116,419 patent/US5372864A/en not_active Expired - Lifetime
-
1994
- 1994-02-16 US US08/197,527 patent/US5384377A/en not_active Expired - Lifetime
- 1994-08-02 MY MYPI94002014A patent/MY111530A/en unknown
- 1994-08-17 HU HU9600512A patent/HU214928B/en not_active IP Right Cessation
- 1994-08-17 EP EP94926521A patent/EP0716666B1/en not_active Expired - Lifetime
- 1994-08-17 PL PL94309635A patent/PL309635A1/en unknown
- 1994-08-17 KR KR1019960701056A patent/KR100335545B1/en not_active IP Right Cessation
- 1994-08-17 DE DE69410277T patent/DE69410277T2/en not_active Expired - Lifetime
- 1994-08-17 RU RU96107237/04A patent/RU2142477C1/en not_active IP Right Cessation
- 1994-08-17 WO PCT/US1994/009294 patent/WO1995006677A1/en not_active Application Discontinuation
- 1994-08-17 CZ CZ96613A patent/CZ61396A3/en unknown
- 1994-08-17 CA CA002170145A patent/CA2170145C/en not_active Expired - Fee Related
- 1994-08-17 BR BR9407453A patent/BR9407453A/en not_active IP Right Cessation
- 1994-08-17 AU AU76334/94A patent/AU680292B2/en not_active Ceased
- 1994-08-17 JP JP7508142A patent/JP3055698B2/en not_active Expired - Fee Related
- 1994-08-17 NZ NZ273139A patent/NZ273139A/en unknown
- 1994-08-17 ES ES94926521T patent/ES2115971T3/en not_active Expired - Lifetime
- 1994-08-17 CN CN94193892A patent/CN1052738C/en not_active Expired - Fee Related
- 1994-08-17 AT AT94926521T patent/ATE166081T1/en active
- 1994-09-05 CO CO94039526A patent/CO4410419A1/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU96107237A (en) | TONERS FOR POLYESTERS | |
KR960704961A (en) | TONER FOR POLYESTERS | |
KR890005576A (en) | Stabilizer for Color Photographic Recording Materials | |
FI843978L (en) | LJUSKAENSLIGA, TRIKLORMETYLGRUPPER INNEHAOLLANDE FOERENINGAR, FOERFARANDE FOER DERAS FRAMSTAELLNING OCH DESSA FOERENINGAR INNEHAOLLANDE LJUSKAENSLIG BLANDNING. | |
KR860002734A (en) | Silver halide color photosensitive material | |
KR850008181A (en) | Yellow Disperse Dye Composition | |
KR930013008A (en) | Disperse dye mixture | |
AR246979A1 (en) | Water soluble disazo compounds, process for their preparation and their use as dyestuffs | |
JPS5652747A (en) | Color photographic material | |
JPS5724941A (en) | Color photographic sensitive material | |
JPS57204038A (en) | Color photosensitive silver halide material | |
JPS5792079A (en) | Liquid crystal composition for color display | |
GB1489087A (en) | Dithianes and dithiolanes | |
JPS56141360A (en) | Fluorescent whitner mixture | |
JPS5533141A (en) | Photosensitive element containing substance forming cyan dye image | |
JPS5767664A (en) | Film forming assistant composition for vinyl polymeric aqueous emulsion | |
JPS57125257A (en) | Stabilized synthetic resin composition | |
JPS5538825A (en) | Colored polyester film | |
DK606286A (en) | ANTHRACYCLIN DERIVATIVES AND MEDICINALS CONTAINING THESE COMPOUNDS | |
JPS5565953A (en) | Silver halide color photographic emulsion | |
JPS56113790A (en) | Improved organic phosphite composition | |
JPS56145946A (en) | Stabilized polyurethane composition | |
JPS57195144A (en) | Polyester composition | |
KR880009096A (en) | Anthraquinone compound, preparation method thereof, and dyeing or printing method of fibers using same | |
JPS5657772A (en) | Photodimerization type photocompound containing melamine group and its preparation |