CA1340754C

CA1340754C - Oil-filled capacitor

Info

Publication number: CA1340754C
Application number: CA000546893A
Authority: CA
Inventors: Keiji Endo; Hideyuki Dohi; Shigenobu Kawakami; Atsushi Sato
Original assignee: Nippon Petrochemicals Co Ltd
Current assignee: Eneos Corp
Priority date: 1987-09-15
Filing date: 1987-09-15
Publication date: 1999-09-21
Anticipated expiration: 2016-09-21

Abstract

An improved oil-filled capacitor which is excellent in low temperature characteristics. The oil-filled capacitor is composed of at least partially a plastics material and is impregnated with an electrical insulating oil which oil is characterized in that it comprises 0 to 100% by weight of a fraction A containing components boiling within the range of 268 to 275°C (atmospheric pressure basis) and 100 to 0% by weight of a fraction B containing components boiling within the range of 280 to 310°C
(atmospheric pressure basis) which fractions are recovered by distillation from the heavy by-product oil that is produced in the preparation of ethylbenzene by alkylating benzene with ethylene in the presence of an alkylation catalyst and the ratio of the integrated intensity as chemical shift at 120 to 155 ppm of the spectrum measured by C13 NMR method to the total integrated intensity at 0 to 155 ppm of the spectrum is 80% or higher with regard to said fraction A and tree same ratio is 72% or higher with regard to said fraction B.

Description

134U?~4 OIL-FILLED CAPACITOR
BACKGROUND OF THE INVENTION
Field of the Invention This :invention relates to an oil-filled capacitor which is impregnated 'with an electrical insulating oil that is prepared frorn the ~by-product oil fractions obtained in the process to prepare ethylbenzene. Furthermore, the invention relatE:s to an oil-filled capacitor which is impregnated with an electrical insulating oil comprising a specific fraction or its mixture derived from the above-mentioned by-product oil.
Description of the Prior Art It is well known that a heavy by-product oil is produced in the process to prepare ethylbenzene by reacting benzene with ethylene in the presence of an alkylation catalyst as disclosed in, for example, U. S. Patent Nos. 4,108,788; 4,111"825; and 4,228,024.
In the same reference, it is described that the fraction having a boi7Ling range of 275 to 420°C is useful as an electrical insulating oil.
The present inventors recovered the fraction described in the abovE: reference by distillation and used it for the impregnation of oil-filled capacitors made by using polypropylene film. However, it was found out that capacitors having excellent characteristics cannot always be made, while the reason for this has not yet been clear.

130?~1 The above by-product oil obtained from the ethylbenzene prE:paration process, however, inevitably contains various uncertain compounds that cannot be determined by analysis, as the general characters of the materials of this kind. The kinds and quantities of these undeterminable compounds are not fixed and, in addition, the boiling points of these compounds are close to or overlapped with one another. Accordingly, it is impossible to isolate any component only by distillation from the by-product oil.
In the case that a fraction having a certain boiling point is recovered, the boiling point of the fraction is indicated by the distilling temperature of the fraction.
In practice, however, the efficiency of the distillation generally depends upon the distilling conditions such as the number of theoretical plates of distillation apparatus, reflux ratio, bottom temperature and other temperature distribution in a distillation column, and the rate of distillation. Even when the distillation temperatures, that is, the boiling points are the same, the kinds and quantities of components in distilled fractions are liable to vary largely.
Owing to the complexity of the origin of by-product oil and operational factors in the distillation of by-product oi:L, it is supposed that an electrical insulating oil having excellent characteristics cannot be obtained only by a simple measure of distillation.

3 - ~34~'~~~
E~RIEF :SUMMARY OF THE INVENTION
In view of the above facts, the present inventors have carried out extensive studies on the preparation of oil-filled capacitors using such by-product oils.
It is, therefore, the primary object of the present invention to provide an oil-filled capacitor which is impregnated with an electrical insulating oil having excellent electrical characteristics that is prepared from the by-product oil in the ethylbenzene preparation.
Another object of the present invention is to provide an oil-filled capacitor which can be produced at low cost without difficulty.
In accordance with the present invention, the oil-filled capacitor is composed of, at least partially, a dielectric substance of plastics material and it is, of course, impregnated with an electrical insulating oil.
The oil is characterized in that it comprises 0 to 1000 by weight, of a fraction A containing components boiling within the range of 268 to 2.'5°C (atmospheric pressure basis) and 100 to Oo by weight of= a fraction B containing components within the range of 280 to 310°C. These fractions are those recovered by distillation from the heavy by-product oil which is produced in the preparation of ethylbenzene by alkylating benzene with ethylene in the presence of an alkylation catalyst and the ratio of the integrated intensity as chemical shift a.t 120 to 155 ppm of the spectrum measured by C13 NMR method to t:he total integrated intensity at 0 to 155 ppm of the spectrum is 80o or higher with regard to the fraction A and the same ratio is 72% or higher with regard to the fraction B.
The objects and features of the present invention will become more apparent in the following description.
DETAILED DESCRIPTION OF THE INVENTION
The method t:o prepare ethylbenzene by alkylating benzene with ethylene in the presence of an alkylation catalyst is widely carried out industrially as a method for preparing th.e raw material of styrene monomer. The by-product oil referred to in the present invention is obtained from such a process for preparing ethylbenzene.
More particularly, a liquid phase alkylation method or a vapor phase alkylation method is generally used for reacting benzene with ethylene. In the liquid phase alkylation method, a F'riedel-Crafts catalyst such as aluminum chloride or a Br~nste~i acid such as p-toluenesulfonic acid or hydrofluoric acid is used. In the vapor phase alkylation method, a synthetic ze:olite such as ZSM-5 or phosphoric acid carried on an appropriate carrier is used. The reaction temperatures are. genez-ally selected from the range of 20 to 175°C in the lic,uid phase alkylation method and 250 to 450°C
in the vapor phase alkylation method.
Through the above reaction, an alkylation product is obtained. This alkylation product comprises unreacted benzene, the aimed ethylbenzene, polyethylbenzene and a heavy by-product oil. The alkylation product is then _ 5 - ~3~~'~5~
subjected to the removal of catalyst, neutralization and washing with water as occasion demands according to the conventional method. The by-product oil used in the present invention is then obtained by removing the unreacted benzene, ethylbenzene, and polyethylbenzene by distillation. Because the by-product oil contains tarry substances and in order to facilitate the below-described distillation operation, the by-product oil is previously subjected to rough distillation at a reduced pressure to obtain a fraction covering a temper-ature range broader than that of the aimed fractions. This fraction obtained in the rough distillation is not especially limited as far as it covers the aimed temperature range.
That is, the fraction is selected from the range in distilling temperatures of 255 to 420°C (atmospheric pressure basis).
From the above by-product oil, the fraction A
containing components having a boiling temperature range of 268 to 275°C (atmospheric pressure basis) and another fraction B containing components having a boiling temperature range of 280 to 310°C (atmospheric pressure basis) are obtained by precision fractional distillation.
As described above, various undeterminable compounds are contained in the by-product oil from ethylbenzene. When heated, these compounds are liable to polymerize, decompose or isomerize. Furthermore, the by-product oil itself is heavy and high in boiling point. Accordingly, the distillation of the by-product oil must be done under reduced pressures.

When it is subjected to distillation at atmospheric pressure, the fvorego:ing ratios of .integrated . intensities cannot reach.the level of 80~ or higher in the fraction A
and the level of 72~ or. higher in. the fraction B. Or, even when the ratio~~ reach these values, the characteristics of_ the electrical insulating oil .is quite poor. The sufficient.
degree of the :reduced pressure may be 200 mmHg or lower, and preferably not higher than 5.0 mmHg. It is undesirable in view of economy.to.reduce the pressure to excess. The precision fractional distillation. can be carried out either in continuous c>r in batch wise operation using one or a plurality of distillation columns. The distillation is carried out by regul,3ting the distilling conditions, for example, the number of theoretical plates of distillation column, the bottom temperature and other temperature distribution in the column, the rate of distillation, and other factors, so as to meet the foregoing conditions.
It is necessary to use a~distillation apparatus ofgenerally 10 or mode, prEsferably 20 br more;. in the theoretical number of plates. In ~t:he event that ahe obtained fraction contains substantially no components boiling, within the above-mentioned' temperature range, the. ratios ne.Yer reach these values andv the electrical characteristics, of the by-product oil cannot be improved. ~~ccordingly, the distillation conditions are to be selected,.
It i:~ inevitable that the ratio of the integrated intensity as~chem-ical shift at 120 to 155.ppm of the spectrum measured by C13 NMR method to the total integrated intensity at 0 to 155 ppm of the spectrum is 800 or higher with regard to the fraction A and the same ratio is 72% or higher with regard to the fraction. B. In connection with the electrical insulating oil used in the present invention, quite excellent electrical characteristics are exhibited by the constituents of the fraction A or those of the fraction B or the syner-gistic effect of both the fractions A and B. In the case that the ratio of the integrated intensity of the spectrum measured by C13 NMR method is lower than 80% in the fraction A or the ratio is lower than 72s in the fraction B, such the synergistic effect cannot be expected.
The electrical insulating oil used in the present invention can comprise the above-described fraction A or the fraction B. It is, however, preferable that the electrical insulating oil comprises a mixture of both the fractions.
That i;s, the preferable electrical insulating oil used for impregnating the oil-filled capacitor is a mixture of 10 to 800, more preferably 20 to 70%, by weight of the fraction A and 90 to 20%, more preferably 80 to 30%, by weight of the fraction B; and the ratio of the integrated intensity as chemical shift at 120 to 155 ppm of the spectrum measured by C13 IVMR method to the total integrated intensity at 0 to 155 ppm of the spectrum is 800 or higher with regard to said fraction A and the same ratio is 720 or higher with regard to said f_~action B.

- 1340' ~4 In the case that the proportion of the fraction A
is less than lOs by weight, that is the proportion of the fraction B is more than 90a by weight, it is less desirable because the corona discharge characteristic of the capacitor which is impregnated with such an electrical insulating oil is impaired. On the other hand, if the proportion of the fraction A exceeds 80o by weight, that is the proportion of the fraction B is less than 20o by weight, it is also less desirable because: the low temperature characteristics of the capacitor which is impregnated with such an electrical insulating oil is impaired.
The elE:ctrical insulating oil prepared as described above is refined if need be and it is used as an impregnating oil for oil-f ille:d capacitors . The ref fining can be done in the process of di.still<~tion of the by-product oil.
Furthermore, in ~~ccord<3nce with uses, it is possible to use the electrical insulating oil by mixing it with well known diaryl alkanes, alkyl biphenyls, alkyl naphthalenes and so forth in arbitrary proportions.
The oil-filled capacitor of the present invention is the one in which at least a part of dielectric substance is composed of a plastics film. As the plastics films, those of polyolefins such as polyethylene, polypropylene and polymethylpentene are desirable. Among them, the film made of polypropylene i.s most preferable. For example, the oil-filled capacitor of the present invention is made by winding a metal foil. such as aluminum foil together with 1340r1~~
polypropylene film, and if necessary also with insulating paper, and impregnating it with the above-described electrical insulating oil according to the conventional method. The oil-filled capacitor in which a metallized plastics film is wound together with a plastic film or insulating paper and then impregnated with an electrical insulating oil is also covered by the present invention.
The dei=ermination in C13 NMR method will be described. The measuring temperature is generally the room temperature. A fraction to be measured is dissolved into a solvent of deutero chloroform to prepare a solution of 10 to 20% by volume. The frequency of measurement can be varied properly, for example, measurement is done at 67.8 MHz.
In the obtained C:13 NMR spectrum, the integrated intensity between 120 to 155 ppm in chemical shift on the basis of tetramethylsilane is measured and then the ratio (%) of this value to the integrated intensity of the total spectrum (0 to 155 ppm) excluding that of the solvent, is obtained.
The numeral on the first decimal place is rounded. In order to improve the quantitative accuracy, the measurement is generally done by the proton complete decoupling method with eliminating the nuclear overhauser effect.
The present ~_nvention will be described in more detail with reference t:o the example of the invention.

1340~~~

E X A M P L E
- Alkylation of Benzene -From the liquid phase alkylation process to prepare ethylbenzene by alkylating benzene with ethylene in the presence of aluminum catalyst, an alkylation product was obtained. The alkylation product consisted of 43.Oo of unreacted benzene, 11.8% of ethylbenzene, 18.3% of polyethyl-benzene and 7.60, all by weight, of heavy by-product oil.
The unreacted benzene, ethylbenzene, and polyethylbenzene were removed by distillation. The remained by-product oil was a viscous black substance. This by-product oil was distilled at a reduced pressure of 10 mmHg to obtain a fraction (hereinafter referred to as "recovered fraction") of 255 to 420°C in distilling temperature (atmospheric pressure basis).
The following fractions were separated from this recovered fraction.
Fraction A
To the bottom of precision fractional distillation column was fed 1600 lit. of the recovered fraction and fraci_ional distillation was carried out at reduced pressure of 5 to 15 mmHg to obtain a fraction A
of 268 to 275°C (atmospheric pressure basis) in distilling temperature.
Packed column:
Diameter.: 400 mm Height: 10.4 m Theoret :cal number of plates : 25 Fraction B
The recovered fraction was distilled using the above distillation column in the like manner as the above to obtain a fraction B of 280 to 310°C (atmospheric pressure basis) in distilling temperature.
Fraction A-1 To the bottom of the following distillation column was fed 1600 lit. of the recovered fraction and fractional distillation was carried out under a reduced pressure below the atmospheric pressure by not less 250 mmHg to obtain a fraction A-1 of 268 to 275°C (atmospheric pressure basis) in distilling temperature.
Packed column:
Diameter: 400 mm Height: 4.0 m Theoretical number of plates: 5 Fraction B-1 The recovered fraction was distilled using the above distillation column in the like manner as the above to obtain a fraction. B-1 of 280 to 310°C (atmospheric pressure basis) in distilling temperature.
- Measurement by C13 NMR Method -Measurement was carried out at the room temperature using a C13 NMR measuring apparatus of Model GX-270 made by Japan Electron Optics Laboratory Co., Ltd. Each fraction was dissolved in a solvent of deutero chloroform to prepare solutions of 15% concentration. The frequency of measurement was 67.8 MHz.

In order to improve the quantitative accuracy, the measurement was done by the proton complete decoupling method with eliminating the nuclear overhauser effect.
In the obtained C13 NMR spectrum, the ratio of integrated intensity of 120 to 155 ppm in chemical shift to the total integrated intensity of the spectrum (0 to 155 ppm) was obtained with regard to each fraction. The results of them are shown in the following Table 1. The standard for the chemical shift was tetramethylsilane.
- Compatibility with Polypropylene Film -Polypropylene films (14 micrometer thick) that were cut into a certain shape, were soaked in the respective fractions at 80°C for 72 hours. After that, the films were taken out and the percentages of changes in volumes of the films were measured, the results of which are shown in Table 1. The smaller value, i.e. the smaller volume change indicates the excellence in size stability, which means that the relevant oil is good in the adaptability to the polypropylene film.
- MeasuremE~nt of Corona Starting Voltage (CSV) and Corona Ending Voltage (CEV) A two-p:Ly polypropylene film (each 14 micrometer thick) as a dielectric substance and aluminum foil as an electrode were pui= together in layers and wound according to the ordinary method to obtain model capacitors for oil impregnation.

_ 13 _ ~3~~~~~
The model capacitors were impregnated with each fraction in vacuo to obtain oil-filled capacitors of 0.4 microfarad in electrostatic capacity.
The corona starting voltages and corona ending voltages of these capacitors at 25°C were measured.
The results are ;shown in Table 1.
Life Test for Capacitors -A two-ply polypropylene film (each 14 micrometer thick) as a dielectric substance and aluminum foil as an electrode were put together in layers and wound according to the ordinary method to obtain model capacitors for oil impregnation.
The model capacitors were impregnated with each fraction in vacuo to obtain oil-filled capacitors of 0.4 microf arad in electrostatic capacity.
These capacitors were applied with prescribed AC
voltages at -35°c~ and the time lengths until the capacitors were broken down were measured to estimate the lives of capacitors. In i=his case, the potential gradients were initiated from 60 V/~ and raised by 10 V/~ at every 48 hours, where the numbers of broken capacitors were counted.
The numbers of c<~pacitors that were used for the test were respectively 10. The :results are shown in the following Table 2.
It wil:L be understood from the results in tables, the fraction A and the fraction B are superior to the recovered fraction even when they are used singly.

- 134U?~~
By mixing the fraction. A and the fraction B, the corona discharge characteristics at the low temperature and the lives of the oil-filled capacitors can be improved as compared with the use of a single fraction A or fraction B.
Furthermore, in the fractions in which the ratios of integrated intensities of C13 NMR method are less than 80% or 72%, it is apparent that the synergistic effect between the fractions A and B cannot be exhibited.

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Claims

1. An oil-filled capacitor comprising:
a dielectric substance of plastic material and impregnated with an electrical insulating oil, said oil comprising:
(a) 10 to 80% by weight of a fraction A, and (b) 90 to 20% by weight of a fraction B:
said fractions A and B having been recovered from the heavy by-product oil that is produced in the preparation of ethylbenzene by alkylating benzene with ethylene in the presence of an alkylation catalyst by fractionally distilling said heavy by-product oil under a reduced pressure of 200 mm Hg maximum and other distillation conditions effective to provide:
said fraction A consisting essentially of components boiling within the range of 268° to 275°C.
(atmospheric pressure basis) and the ratio of the integrated intensity as chemical shift at 120 to 155 ppm of the spectrum measured by C13 NMR method to the total integrated intensity at 0 to 155 ppm of the spectrum is 80% or higher, and said fraction B consisting essentially of components boiling within the range of 280° to 310°C.
(atmospheric pressure basis) and the ratio of the integrated intensity as chemical shift at 120 to 150 ppm of the spectrum measured by C13 NMR method to the total integrated intensity at 0 to 155 ppm of the spectrum is 72% or higher.

2. The oil-filled capacitor in Claim 1, wherein said plastics material is polyolefin.

3. The oil-filled capacitor in Claim 1, wherein said capacitor is made by winding at least a plastics film and a metal foil.

4. The oil-filled capacitor in Claim 1, wherein said alkylation catalyst is Friedel-Crafts catalyst.

5. A meahod for producing an oil-filled capacitor which is composed of, at least partially, a dielectric substance of plastics material, said method comprising the steps of distilling the heavy by-product oil which is produced in the preparation of ethylbenzene by alkylating benzene with ethylene in the presence of an alkylation catalyst; to obtain an electrical insulating oil comprising 10 t:o 80% by weight. of a fraction A containing components boiling within the range of 268° to 275°C.
(atmospheric pressure basis) and 90 to 20% by weight of a fraction B containing components boiling within the range of 280 to 310°C. (atmospheric pressure basis), the operation of said distillation being carried out in such a manner that the ratio of the integrated intensity as chemical shift at 120 to 155 ppm of the spectrum measured by C13 NMR method to the total integrated intensity at 0 to 155 ppm of the spectrum is 80% or higher with regard to said fraction A and the same ratio is 72%
or higher with regard to said fraction B, respectively; and impregnating a capa<:itor element with the thus obtained electrical insulating oil.

6. The method for producing an oil-filled capacitor in Claim 5, wherein said. plastics material is polyolefin.

7. The method for producing an oil-filled capacitor in Claim 5, wherein said capacitor is made by winding at least a plastics film and <~ metal foil.

8. The method for producing an oil-filled capacitor in Claim 5, wherein said alkylation catalyst is a Friedel-Crafts catalyst.

9. A method for producing an oil-filled capacitor comprising a dielectric substance of plastic material and impregnated with an electrical insulating oil, said oil comprising:
(a) 10 to 80% by weight of a fraction A, and (b) 90 to 20% by weight of a fraction B:
said fractions A and B having been recovered from the heavy by-product oil that is produced in the preparation of ethylbenzene by alkylating benzene with ethylene in the presence of an alkylation catalyst;
said method comprising the steps of fractionally distilling said heavy by-product oil under a reduced pressure of 200 mm Hg maximum and other distillation conditions effective to provide:
said fraction A consisting essentially of components boiling within the range of 268° to 275°C.
(atmospheric: pressure basis) and the ratio of the integrated intensity as chemical shift at 120 to 155 ppm of the spectrum measured by C13 NMR method to the total integrated intensity at 0 to 155 ppm of the spectrum is 80% or higher, and said fraction B consisting essentially of components boiling within the range of 280° to 310°C.
(atmospheric pressure basis) and the ratio of the integrated intensity as chemical shift at 120 to 150 ppm of the spectrum measured by C13 NMR method to the total integrated intensity at 0 to 155 ppm of the spectrum is 72% or higher; and impregnating a capacitor element with the thus obtained electrical insulating oil.

10. The method for producing an oil-filled capacitor in Claim 9, wherein said plastics material is polyolefin.

11. The method for producing an oil-filled capacitor in Claim 9, wherein said capacitor is made by winding at least a plastics film and a metal foil.

12. The method for producing an oil-filled capacitor in oil Claim 9, wherein said alkylation catalyst is a Friedel-Crafts catalyst.