CN1737027A - A kind of C 9The preparation method of petroleum coal resin - Google Patents
A kind of C 9The preparation method of petroleum coal resin Download PDFInfo
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- CN1737027A CN1737027A CN 200410056912 CN200410056912A CN1737027A CN 1737027 A CN1737027 A CN 1737027A CN 200410056912 CN200410056912 CN 200410056912 CN 200410056912 A CN200410056912 A CN 200410056912A CN 1737027 A CN1737027 A CN 1737027A
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Abstract
The present invention relates to a kind of C of utilization
9The petroleum fractions preparation is applicable to the C that the starching of paper industry paper is used
9The preparation method of petroleum coal resin is at first to C
9Petroleum fractions is carried out underpressure distillation under the pressure of 0.08～0.09MPa, collect 90～120 ℃ C
9Cut adds 2～10% cis-butenedioic anhydride, 89～97% C successively as reaction raw materials in the reactor of electric mixer is housed
9Cut and 0.2～1% BF
3-etherate, under 50～80 ℃ of temperature, reacted 3～5 hours, with NaOH and water polymer fluid is alternately washed, to neutral, then under 0.08～0.095MPa vacuum tightness to the polymer fluid underpressure distillation, after treating that temperature decline is no longer risen, promptly get product, reaction conditions gentleness of the present invention, reaction solution post-processing operation process simply and not produces emulsion, the products obtained therefrom steady quality, and productive rate is the highest can to reach 53.26%, the active ingredient transformation efficiency is up to 95%, and its acid number, bromine number, form and aspect, softening temperature all can reach requirement.
Description
Technical field
The present invention relates to a kind of C of utilization
9The petroleum fractions preparation is applicable to the C that the starching of paper industry paper is used
9The preparation method of petroleum coal resin.
Background technology
World developed country produces C at present
9The trend forward scale of petroleum resin maximizes, diversification of varieties, and the direction of trade mark seriation develops.By contrast, the petroleum resin industry of China also is in the starting stage.Because the raw material supply instability of petroleum resin, mixed fraction lacks necessary separation and purification means, and production technology is backward relatively, thereby causes the color and luster of resin darker, and less stable, and its range of application is very limited.Most of device industrial scale is little, and kind is single, and quality product is not high, main quality index instability such as product colourity, softening temperature particularly, and many devices are in and stop production or half end-of-life state.At present domestic and international C
9The development of petroleum resin mainly concentrates on the method for modifying of petroleum resin and explores, modification is development in two directions mainly: the one, and it is being to introduce polar group in the oil-soluble petroleum resin molecule to make it to become certain polarity is arranged originally that chemistry improves promptly, even water miscible polymkeric substance; The 2nd, thus hydrogenation modification makes the unsaturated link(age) in the petroleum resin molecule obtain saturated its color and luster that improves.The C of comprehensive patent documentation both at home and abroad record
9Petroleum resin modified technology mainly is the improvement of catalyzer, the pre-treatment and the particular monomers modification technology of petroleum fractions.It mainly is the preparation loaded catalyst that catalyzer improves technology, and the reaction solution that obtains like this is difficult for emulsification, is easy to handle; Complicated raw materials pretreatment production cost is too high, is not suitable for applying; The petroleum resin production cost of particular monomers modification is also very high, mainly applies to special occasions.
Summary of the invention
The object of the present invention is to provide a kind of preparation method simple, the reaction conditions gentleness, reaction solution post-processing operation process simply and not produces emulsion, the stay-in-grade C of products obtained therefrom
9The preparation method of petroleum coal resin.
The technical solution used in the present invention is in order to achieve the above object: at first with the by product C of ethylene cracker
990～120 ℃ C is collected in cut underpressure distillation under the pressure of 0.08～0.09Mpa
9Cut is as C
9The reaction raw materials of petroleum resin; In having the reactor of stirring, it is 2～10% cis-butenedioic anhydride, 89～97% C that temperature is controlled at 30 ℃ of next coming in order adding mass percents
9Cut and 0.2～1% BF
3-etherate, heating up in the reinforced back that finishes, reacted 3～5 hours under 50～80 ℃ of temperature, obtains polymer fluid; Polymer fluid is added in the NaOH solution of concentration 5% and soaked 25～35 minutes, and then with 65～75 ℃ hot wash, alkali cleaning-washing hockets up to polymer fluid is washed till neutrality; To the polymer fluid heating, rise when temperature rises to no longer under 0.08～0.095MPa vacuum tightness, temperature stops distillation when descending once again, and products obtained therefrom is light yellow transparence fluid, and the cooling back is a brittle solid.
Raw materials pretreatment and analysis
The by product C of ethylene cracker
9Cut is the important source material of synthesizing petroleum resin, because of ethylene unit uses raw material difference, by-product C
9Cut amount and composition also have very big-difference, and it influences C
9The quality of petroleum resin and performance.C
9Form extremely complexity, detectable complex component is kind more than 150 nearly, and changes with the difference of cracking stock, cracking severity, cracking technology.But having only 30%～60% polymerizable components is active ingredient, and all the other are inactive ingredients.Active ingredient mainly is vinylbenzene and derivative, indenes and derivative, dicyclopentadiene etc.C of the present invention
9Raw material is provided by Lanzhou chemical industrial company, wherein contains the darker impurity of more color, need carry out feed purification.With C
9Raw material is under vacuum tightness 0.08～0.09Mpa, and 90～120 ℃ cut is collected in underpressure distillation, selects for use these cuts as C
9The reaction raw materials of petroleum resin.Analyze the composition of this temperature range cut with gas chromatography-mass spectrum (GC-MS) combined instrument, wherein the result of main component is as shown in table 1:
Table 1C
9Fractions consisting
| Phenylallene | 18.81％ |
| Vinylbenzene and derivative thereof | 1.63％ |
| Indenes and derivative thereof | 14.6％ |
| Cyclopentadiene | 3.83％ |
| Dicyclopentadiene | 17.37％ |
As seen be used for polymeric C by table 1
9The composition of activeconstituents is about 56% in the cut.
Polyreaction
The present invention adopts catalyst polymerization to produce petroleum resin.In having the reactor of stirring, it is 2～10% MALEIC ANHYDRIDE, 89～97% C that temperature is controlled at 30 ℃ of next coming in order adding mass percents
9Cut and 0.2～1% BF
3-etherate, heating up in the reinforced back that finishes, reacted 3～5 hours under 50～80 ℃ of temperature, obtains polymer fluid.
The processing condition of polyreaction are determined
(1) selection of catalysts and consumption
Catalyst polymerization synthesizes C
9The catalyzer that petroleum resin are commonly used has AlCl
3And BF
3-etherate.Experimental result shows, uses AlCl
3When making catalyzer, catalyzer is easily bonding with reactant in the reaction process, in the water washing process emulsification serious, make the separation of catalyzer become quite difficult.And AlCl
3Be easy to inactivation, want strict control anhydrous in the reaction system, C
9The reinforced need drips adding, otherwise all very easily causes implode, and needs to add solvent.And BF
3Water washing process did not produce emulsification when-etherate was made catalyzer, and the polymer fluid layering is clear, and BF
3-etherate is made catalyzer C when reinforced
9Can directly once add, not need progressively to drip, need not add solvent, can not cause the implode phenomenon.
The present invention selects BF for use
3-etherate is made catalyzer.When other condition was identical, catalyst levels was shown in Table 2 the influence of product index.
Table 2 catalyst B F
3-etherate consumption is to the influence of product index
| The catalyst quality mark | Product yield | Bromine number (g/100gBr) | Acid number (mgKOH/g) | Form and aspect (Gardner) | Softening temperature (℃) |
| 0.2％ | 50.83％ | 26.67 | 0.27 | 4.4 | 110 |
| 0.3％ | 51.04％ | 33.44 | 0.36 | 5.1 | 106 |
| 0.5％ | 53.26％ | 35.32 | 0.35 | 5.6 | 98 |
| 1.0％ | 51.44％ | 42.23 | 0.82 | 7.3 | 86 |
As can be seen from Table 2, BF
3-etherate mass percent is 0.5% o'clock, and productive rate can reach 53.26%, and the active ingredient transformation efficiency then can reach 95%, and form and aspect are less than 6, and softening temperature, bromine number and acid number size all can reach requirement.Influence is not very big to catalyst levels to productive rate between 0.1～1%, becomes big but catalytic amount increases the product bromine number, and softening temperature reduces, and form and aspect are deepened, and consider BF from economic angle
3-ether consumption is taken as 0.5% the best.
(2) material rate and feed way
Select BF for use
3C when-etherate is made catalyzer
9Cut can directly feed in raw material, and does not therefore need other solubilizing agent dilution.The desolventizing in the post-processing operation and the recycling step of solvent have been exempted like this.Feed way is to add cis-butenedioic anhydride earlier, then with C
9Directly once add reaction flask, again with BF
3-etherate adds by needle cylinder injection, can divide according to circumstances several times to add.
Cis-butenedioic anhydride is as C
9The modified monomer of raw material, its consumption is shown in Table 3 the influence of quality product.
Table 3 cis-butenedioic anhydride quality is to the influence of product index
| The massfraction of cis-butenedioic anhydride | Product yield | Form and aspect (Gardner) | Bromine number (g/100gBr) |
| 2％ | 51.15％ | 6.5 | 41.2 |
| 4％ | 52.35％ | 6.4 | 35.3 |
| 6％ | 53.26％ | 6.1 | 32.2 |
| 10％ | 53.13％ | 7.5 | 31.4 |
As seen from Table 3, the cis-butenedioic anhydride quality is 6% o'clock, and index such as the highest and form and aspect of product yield is all better.When the cis-butenedioic anhydride consumption increased, the resin productive rate increased to some extent, when add-on increases to more than 10%, when other conditions are constant, the resin productive rate does not enlarge markedly, and the condensation of part white solid material is arranged on prolong during underpressure distillation, illustrates that cis-butenedioic anhydride participates in reaction fully.Therefore the cis-butenedioic anhydride add-on is that 6% o'clock of total amount just can reach best effect.
(3) polymerization temperature, time
C
9Need certain heat when two keys are opened in the cut, temperature is low excessively, and reaction can't be carried out, and too highly causes implode easily.Particularly the initial reaction stage temperature must be controlled well, and temperature is controlled at below 30 ℃ when beginning to feed in raw material, and slowly heats up after having fed in raw material again.Because polyreaction is thermopositive reaction, if temperature of reaction is too high, reaction heat can not in time shift out, and not only increases volatilization loss, the reduction product yield of reaction mass, also makes speed of reaction too fast, and the petroleum resin products form and aspect are deepened, and influence quality product.Reaction times has influence on the degree of polyreaction, and the time, too short reaction was insufficient, oversize need not.BF
3When-ether was made catalyzer, polymerization temperature and time were to the influence of product yield as shown in Figure 1.
As seen from Figure 1, increase temperature again after temperature of reaction is elevated to 75 ℃, how productive rate increases hardly, and the resin form and aspect are deepened.We test the application water-bath and come control reaction temperature, and the too high moisture content volatilization of temperature is very fast, needs constantly to replenish.So taking all factors into consideration temperature of reaction from experimental result and economic angle should be controlled at about 70 ℃.Along with the prolongation of polymerization time, product yield increases, and foxy is little, but polymerization time increase to certain value after the productive rate ascensional range obviously reduce, therefore too prolong the reaction times and do not have practical significance.Consider that from industrial production and economic benefit polymerization time was controlled at 3～5 hours.
The aftertreatment technology condition is determined
Aftertreatment mainly comprises removing of catalyzer and making with extra care of resin.Removing catalyzer from reaction solution also is the key link that influences the petroleum resin products performance, not only influences resin quality, and influences the carrying out of whole aftertreatment technology.
(1) catalyzer removes
The method that removes at present catalyzer both at home and abroad is a lot, there are washing, alcohol to wash and three kinds of carclazyte calcium hydroxide dry-cleaning, alcohol is washed and technological operation cost height such as dry-cleaning, and need to increase the subsequent recovery treatment step, the present invention adopts washing process, adopts alkali cleaning-washing to hocket, and first after being about to polymer fluid and having reacted is 5% NaOH solution soaking 25～35 minutes with concentration, and then, add alkali when needing up to being washed till neutrality with hot water gradation washing.This washing methods can not produce emulsion substantially.Wherein Shui Xi water temperature also is the factor that influences washing effect, and water temperature is too low can not thoroughly to be removed catalyzer, and washing effect is bad, too high easy generation emulsion, and through experimental verification, water temperature is advisable with 65～75 ℃.This method equipment is simple, lower, the no waste residue of cost, effective.
(2) resin is refining
Raw material leaves the inactive ingredients of not participating in polyreaction and exists behind catalyzed polymerization.This unreacted reactant such as insufficient removing not only can be reduced the softening temperature of resin, and performances such as the thermotolerance of resin and form and aspect are significantly reduced, and have therefore selected distillation under vacuum that it is removed.Recyclable the recycling of isolated not polymeric component.Underpressure distillation must be distilled thoroughly, under 0.08～0.095MPa vacuum tightness, no longer rises after temperature rises to about 120 ℃, just can stop when temperature descends once again having distilled.Products obtained therefrom is light yellow transparence fluid, and the cooling back is a brittle solid.
The product that adopts preparation method of the present invention to make, productive rate is the highest can to reach 53.26%, and the active ingredient transformation efficiency is up to 95%, its acid number 0.27～0.82mgKOH/g, bromine number 26.67～42g/100gBr. form and aspect 4.4～7.3Gardner, softening temperature all can reach requirement for 86～110 ℃.
Product index is measured
(1) productive rate of product is determined by the ratio of quality product and raw materials quality, does not consider the per-cent of activeconstituents when raw materials quality is calculated.C
9The cut quality is calculated by density 0.85g/ml.
(2) bromine number: carry out with reference to GB GB11135-89 and ISO3499-1976 (E).
(3) acid number: undertaken by GB GB264-83.
(4) form and aspect Gardner: carry out with reference to GB GB6540-86.
(5) softening temperature: undertaken by GB GB9284-88.
C of the present invention
9Petroleum fractions through after the simple pre-treatment with BF
3-etherate, the copolymerization of cis-butenedioic anhydride process, the reaction conditions gentleness, reaction solution post-processing operation process simply and not produces emulsion, the products obtained therefrom steady quality, the every index of product reaches requirement.
Description of drawings
Fig. 1 is polymerization temperature of the present invention and the time influence curve distribution plan to productive rate.
Embodiment
Embodiment 1
By product C with Lanzhou chemical industrial company ethylene cracker
9Cut is done raw material, with C
990 ℃ C is collected in cut underpressure distillation under the pressure of 0.08Mpa
9Cut is selected these C for use
9Cut is as C
9The reaction raw materials of petroleum resin; In having the reactor of stirring (60W, 3000 rev/mins, Changzhou state China motor company), it is 10% MALEIC ANHYDRIDE, 89% C that temperature is controlled at 30 ℃ of next coming in order adding mass percents
9Cut and 1% BF
3-etherate, heat up in the reinforced back that finishes, and reaction is 3 hours under 80 ℃ of temperature, obtains polymer fluid; It is to soak 25 minutes in 5% the NaOH solution that polymer fluid is added concentration, and then with 75 ℃ hot wash, alkali cleaning-washing hockets up to polymer fluid is washed till neutrality; To the polymer fluid heating, no longer rise when temperature rises to about 120 ℃ under 0.08MPa vacuum tightness, temperature stops distillation when descending once again, and products obtained therefrom is light yellow transparence fluid, and the cooling back is a brittle solid.
Embodiment 2
By product C with Lanzhou chemical industrial company ethylene cracker
9Cut is done raw material, with C
9110 ℃ C is collected in raw material underpressure distillation under the pressure of 0.09Mpa
9Cut is selected these C for use
9Cut is as C
9The reaction raw materials of petroleum resin; In having the reactor of stirring, it is 2% MALEIC ANHYDRIDE, 97% C that temperature is controlled at 30 ℃ of next coming in order adding mass percents
9Cut and 1% BF
3-etherate, heat up in the reinforced back that finishes, and reaction is 5 hours under 70 ℃ of temperature, obtains polymer fluid; It is to soak 30 minutes in 5% the NaOH solution that polymer fluid is added concentration, and then with 65 ℃ hot wash, alkali cleaning-washing hockets up to polymer fluid is washed till neutrality; To the polymer fluid heating, no longer rise when temperature rises to about 120 ℃ under 0.095MPa vacuum tightness, temperature stops distillation when descending once again, and products obtained therefrom is light yellow transparence fluid, and the cooling back is a brittle solid.
Embodiment 3
By product C with Lanzhou chemical industrial company ethylene cracker
9Cut is done raw material, with C
9120 ℃ C is collected in raw material underpressure distillation under the pressure of 0.085Mpa
9Cut is selected these C for use
9Cut is as C
9The reaction raw materials of petroleum resin; In having the reactor of stirring, it is 6% MALEIC ANHYDRIDE, 93.8% C that temperature is controlled at 30 ℃ of next coming in order adding mass percents
9Cut and 0.2% BF
3-etherate, heat up in the reinforced back that finishes, and reaction is 4 hours under 50 ℃ of temperature, obtains polymer fluid; It is to soak 35 minutes in 5% the NaOH solution that polymer fluid is added concentration, and then with 70 ℃ hot wash, alkali cleaning-washing hockets up to polymer fluid is washed till neutrality; To the polymer fluid heating, no longer rise when temperature rises to about 120 ℃ under 0.09MPa vacuum tightness, temperature stops distillation when descending once again, and products obtained therefrom is light yellow transparence fluid, and the cooling back is a brittle solid.
Embodiment 4
By product C with Lanzhou chemical industrial company ethylene cracker
9Cut is done raw material, with C
9100 ℃ C is collected in raw material underpressure distillation under the pressure of 0.08Mpa
9Cut is selected these C for use
9Cut is as C
9The reaction raw materials of petroleum resin; In having the reactor of stirring, it is 4% MALEIC ANHYDRIDE, 95.5% C that temperature is controlled at 30 ℃ of next coming in order adding mass percents
9Cut and 0.5% BF
3-etherate, heat up in the reinforced back that finishes, and reaction is 5 hours under 60 ℃ of temperature, obtains polymer fluid; It is to soak 28 minutes in 5% the NaOH solution that polymer fluid is added concentration, and then with 72 ℃ hot wash, alkali cleaning-washing hockets up to polymer fluid is washed till neutrality; To the polymer fluid heating, no longer rise when temperature rises to about 120 ℃ under 0.085MPa vacuum tightness, temperature stops distillation when descending once again, and products obtained therefrom is light yellow transparence fluid, and the cooling back is a brittle solid.
Claims (3)
1, a kind of C
9The preparation method of petroleum coal resin is characterized in that:
1) raw materials pretreatment: with C
990～120 ℃ C is collected in raw material underpressure distillation under the pressure of 0.08～0.09Mpa
9Cut is as C
9The reaction raw materials of petroleum resin;
2) polyreaction: in having the reactor of stirring, temperature is controlled at below 30 ℃, adds mass percent successively and be 2～10% MALEIC ANHYDRIDE, 89～97% C
9Cut and 0.2～1% BF
3-etherate, heating up in the reinforced back that finishes, reacted 3～5 hours under 50～80 ℃ of temperature, obtains polymer fluid;
3) removing of catalyzer: polymer fluid is added in the NaOH solution of concentration 5% and soaked 25～35 minutes, and then with 65～75 ℃ hot wash, alkali cleaning-washing hockets up to polymer fluid is washed till neutrality;
4) resin is refining: to the polymer fluid heating, rise when temperature rises to no longer under 0.08～0.095MPa vacuum tightness, temperature stops distillation when descending once again, obtain product.
2, a kind of C according to claim 1
9The preparation method of petroleum coal resin is characterized in that: BF
3The mass percent of-etherate is 0.5%.
3, a kind of C according to claim 1
9The preparation method of petroleum coal resin is characterized in that: the mass percent of MALEIC ANHYDRIDE is 6%.
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| CNB2004100569127A CN1325526C (en) | 2004-08-20 | 2004-08-20 | C9 solid petroleum resin preparation method |
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|---|---|---|---|
| CNB2004100569127A CN1325526C (en) | 2004-08-20 | 2004-08-20 | C9 solid petroleum resin preparation method |
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| CN1737027A true CN1737027A (en) | 2006-02-22 |
| CN1325526C CN1325526C (en) | 2007-07-11 |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102086251A (en) * | 2010-12-27 | 2011-06-08 | 淄博鲁华泓锦化工股份有限公司 | Continuous alkali washing method of C5 petroleum resin |
| CN104693358A (en) * | 2015-02-12 | 2015-06-10 | 新疆独山子天利实业总公司 | Method for lowering emulsification of m-pentadiene petroleum resin |
| CN109641996A (en) * | 2016-06-30 | 2019-04-16 | 可隆工业株式会社 | Curable Petropols, Its Preparation Method And Use |
| CN111909315A (en) * | 2020-08-06 | 2020-11-10 | 抚顺齐隆化工有限公司 | Method for removing cationic catalyst in short-chain olefin petroleum resin |
| CN112661905A (en) * | 2020-12-24 | 2021-04-16 | 广东新华粤石化集团股份公司 | C9 petroleum resin and preparation method thereof |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5331241B1 (en) * | 1967-03-31 | 1978-09-01 | ||
| CN1033814C (en) * | 1993-07-06 | 1997-01-15 | 大庆石油学院 | Water-soluble carbon pellet petroleum resin |
| JP3379448B2 (en) * | 1998-09-30 | 2003-02-24 | 荒川化学工業株式会社 | Production method of hydrogenated C9 petroleum resin and hydrogenated C9 petroleum resin obtained by the production method |
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2004
- 2004-08-20 CN CNB2004100569127A patent/CN1325526C/en not_active Expired - Fee Related
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102086251A (en) * | 2010-12-27 | 2011-06-08 | 淄博鲁华泓锦化工股份有限公司 | Continuous alkali washing method of C5 petroleum resin |
| CN102086251B (en) * | 2010-12-27 | 2012-08-08 | 淄博鲁华泓锦化工股份有限公司 | Continuous alkali washing method of C5 petroleum resin |
| CN104693358A (en) * | 2015-02-12 | 2015-06-10 | 新疆独山子天利实业总公司 | Method for lowering emulsification of m-pentadiene petroleum resin |
| CN109641996A (en) * | 2016-06-30 | 2019-04-16 | 可隆工业株式会社 | Curable Petropols, Its Preparation Method And Use |
| US11655398B2 (en) | 2016-06-30 | 2023-05-23 | Kolon Industries, Inc. | Curable petroleum resin, preparation method therefor, and use thereof |
| CN111909315A (en) * | 2020-08-06 | 2020-11-10 | 抚顺齐隆化工有限公司 | Method for removing cationic catalyst in short-chain olefin petroleum resin |
| CN111909315B (en) * | 2020-08-06 | 2022-10-11 | 抚顺齐隆化工有限公司 | Method for removing cationic catalyst in short-chain olefin petroleum resin |
| CN112661905A (en) * | 2020-12-24 | 2021-04-16 | 广东新华粤石化集团股份公司 | C9 petroleum resin and preparation method thereof |
| CN112661905B (en) * | 2020-12-24 | 2023-05-16 | 广东新华粤石化集团股份公司 | C9 petroleum resin and preparation method thereof |
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| Publication number | Publication date |
|---|---|
| CN1325526C (en) | 2007-07-11 |
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