RU96107237A - TONERS FOR POLYESTERS - Google Patents

TONERS FOR POLYESTERS

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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
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Russia
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alkyl
alkylene
substituted
group
hydrogen
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RU96107237/04A
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Russian (ru)
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RU2142477C1 (en
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Макс Аллен Уивэр
Вэйн Рэйтон Пруитт
Джерри Фауст Родес
Самуил Давид Хилберт
Уильям Уитфилд Пэрхэм
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Истмэн Кемикал Компани
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Priority claimed from US08/116,419 external-priority patent/US5372864A/en
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1. Литой полиэфир или полиэфир в виде фибрилл, сополимеризованный в достаточном для усиления свойственной этому полиэфиру белизны количестве по меньшей мере одного синего соединения 1,4-бис(2,6-диалкиданилино)антрахинона, имеющего формулу I:
###1
в которой R выбирают из группы, содержащей водород, C1 - C6-алкил, галоген, карбокси и C1 - C6
Figure 00000001
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
Figure 00000001
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.
2. Полиэфир согласно п. 1, отличающийся тем, что синее соединение(я) антрахинона соответствуют приведенной выше структуре (I), в которой R представляет собой водород; R1 и R2 независимо друг от друга выбирают из метила и этила; R3 представляет собой водород, метил или бром; R4 представляет собой водород, C1 - C4-алкил или арил; R5 выбирают из группы, содержащей C1 - C6-алкилен, C1 - C4-алкилен-O-C1 - C4-алкилен, -CH2C6H10CH2-, арилен или -CH2-арилен-, а красный компонент соответствует формуле (V), в которой R7 представляет собой C1 - C6-алкокси, а R4 и R5 имеют значения, определенные в пункте 1 патентной формулы.2. The polyester according to claim 1, characterized in that the blue compound (s) of anthraquinone correspond to the above structure (I), in which R is hydrogen; R 1 and R 2 are independently selected from methyl and ethyl; R 3 is hydrogen, methyl or bromo; R 4 represents hydrogen, C 1 - C 4 -alkyl or aryl; R 5 is selected from the group containing C 1 - C 6 alkylene, C 1 - C 4 alkylene-OC 1 - C 4 alkylene, -CH 2 C 6 H 10 CH 2 -, arylene or -CH 2 -arylene and the red component corresponds to the formula (V) in which R 7 represents C 1 - C 6 -alkoxy, and R 4 and R 5 have the meanings defined in paragraph 1 of the patent formula. 3. Полиэфир по п.1 или 2, отличающийся тем, что концентрации синего и красного соединений, взятые вместе, составляют от ~ 0.5 ppm до ~ 10 ppm. 3. The polyester according to claim 1 or 2, characterized in that the concentrations of the blue and red compounds, taken together, range from ~ 0.5 ppm to ~ 10 ppm. 4. Полиэфир по п.1 или 2, отличающийся тем, что суммарная концентрация синего и красного соединений составляет от 1 до 7 ppm, а концентрация красного соединения(ий) составляет от 0,5 до 3 ppm. 4. The polyester according to claim 1 or 2, characterized in that the total concentration of blue and red compounds is from 1 to 7 ppm, and the concentration of the red compound (s) is from 0.5 to 3 ppm. 5. Полиэфир согласно пп.1, 2, 3 или 4, отличающийся тем, что соединение формулы (I) представляет собой:
###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
Figure 00000002
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
Figure 00000002
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).
9. Метод по п.8, в котором синее соединение антрахинона соответствует приведенной выше структуре (I), в которой R1 и R2 независимо друг от друга выбирают из метила и этила; R3 представляет собой водород, метил или бром; R4 представляет собой водород, C1 - C4-алкил или арил; R5 выбирают из группы, содержащей C1 - C6-алкилен, C1 - C4-алкилен-O-C1 - C4-алкилен, -CH2C6H10CH2-, арилен или -CH2-арилен-, а красный компонент соответствует формуле (V), в которой R7 представляет собой C1 - C6-алкокси, и отличающийся тем, что суммарная концентрация синего и красного компонентов составляет от ~ 0.5 до ~ 10 ppm.9. The method of claim 8, in which the blue anthraquinone compound corresponds to the above structure (I), in which R 1 and R 2 are independently selected from methyl and ethyl; R 3 is hydrogen, methyl or bromo; R 4 represents hydrogen, C 1 - C 4 -alkyl or aryl; R 5 is selected from the group containing C 1 - C 6 alkylene, C 1 - C 4 alkylene-OC 1 - C 4 alkylene, -CH 2 C 6 H 10 CH 2 -, arylene or -CH 2 -arylene and the red component corresponds to the formula (V), in which R 7 represents C 1 - C 6 alkoxy, and characterized in that the total concentration of the blue and red components is from ~ 0.5 to ~ 10 ppm. 10. Метод по п. 8 или 9, в котором синее соединение I представляет собой:
###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
Figure 00000003
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
Figure 00000003
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.
12. Формованное или профилированное изделие, содержащее полиэфир согласно любому из пунктов патентной формулы с 1 по 7. 12. A molded or shaped product containing a polyester according to any one of claims 1 to 7.
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Families Citing this family (149)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

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