CN113087903A - High-temperature-resistant modified polyaspartic acid scale inhibitor and preparation method and use method thereof - Google Patents
High-temperature-resistant modified polyaspartic acid scale inhibitor and preparation method and use method thereof Download PDFInfo
- Publication number
- CN113087903A CN113087903A CN202110287663.6A CN202110287663A CN113087903A CN 113087903 A CN113087903 A CN 113087903A CN 202110287663 A CN202110287663 A CN 202110287663A CN 113087903 A CN113087903 A CN 113087903A
- Authority
- CN
- China
- Prior art keywords
- polyaspartic acid
- modified polyaspartic
- scale inhibitor
- high temperature
- polysuccinimide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/1092—Polysuccinimides
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F5/00—Softening water; Preventing scale; Adding scale preventatives or scale removers to water, e.g. adding sequestering agents
- C02F5/08—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents
- C02F5/10—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances
- C02F5/12—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances containing nitrogen
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/10—Geothermal energy
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Abstract
本发明公开了一种耐高温的改性聚天冬氨酸阻垢剂及其制备方法和使用方法，属于化学合成技术领域，本发明以马来酸酐和尿素为原料，在混酸溶液中反应，得到聚琥珀酰亚胺；将聚琥珀酰亚胺和脯氨酰胺经开环接枝反应，制得耐高温的改性聚天冬氨酸阻垢剂。本发明制备的含氮杂环小分子改性聚天冬氨酸属于无磷环境友好型阻垢剂，克服了现有聚天冬氨酸高温下阻垢效果较差的缺点，对碳酸钙型结垢体系具备优异的阻垢性能，适用于城市地热供暖系统、油井开采生产等存在局部高温的水循环系统。
The invention discloses a high temperature-resistant modified polyaspartic acid scale inhibitor, a preparation method and a use method thereof, and belongs to the technical field of chemical synthesis. The invention uses maleic anhydride and urea as raw materials, and reacts in a mixed acid solution, The polysuccinimide is obtained; the polysuccinimide and the prolineamide are subjected to a ring-opening graft reaction to obtain a high temperature-resistant modified polyaspartic acid scale inhibitor. The nitrogen-containing heterocyclic small-molecule modified polyaspartic acid prepared by the invention belongs to a phosphorus-free environment-friendly scale inhibitor, overcomes the disadvantage of poor scale inhibition effect of the existing polyaspartic acid at high temperature, and is not suitable for calcium carbonate type. The scaling system has excellent scale inhibition performance and is suitable for water circulation systems with local high temperature such as urban geothermal heating systems, oil well production and production.
Description
Technical Field
The invention belongs to the technical field of chemical synthesis, and relates to a high-temperature-resistant polyaspartic acid scale inhibitor, and a preparation method and a use method thereof.
Background
A large amount of anions and cations are often dissolved in an industrial water system, and when the pressure, temperature, concentration and other changes occur in the water using process, the concentration of inorganic salt ions in the system is over saturated, and scale is further precipitated to form scale, so that pipeline blockage can be caused in serious conditions, the heat transfer efficiency is influenced, and potential safety hazards and economic losses are brought to industrial production. Scaling phenomena in occasions of industrial water circulation cooling designed by various industrial processes such as geothermal resource application, reverse osmosis, multi-stage flash evaporation, multi-effect distillation and the like are very common, and the types of generated scales mainly comprise calcium carbonate, calcium sulfate, calcium phosphate, barium sulfate, iron oxide and the like, wherein the calcium carbonate scales are the most common. The most common treatment mode is to inhibit scaling by adding a scale inhibitor, and the addition of a small amount of scale inhibitor can not only play a scale inhibition effect, but also have corrosion inhibition and bacteriostasis effects on metal pipelines. At present, common industrial scale inhibitors comprise phosphorus-rich scale inhibitors such as inorganic phosphate, organic phosphonic acid and the like, which have excellent scale inhibition performance, but cannot meet increasingly strict environmental protection requirements due to the existence of phosphorus. Therefore, the development of green, non-toxic, biodegradable, environmentally friendly scale inhibitors is a necessary trend in the field.
Polyaspartic Acid (PASP) and polyepoxysuccinic acid (PESA) are considered as the most promising new environmentally friendly scale inhibitors. The polyaspartic acid has very excellent scale inhibition effect on calcium carbonate or calcium sulfate scale, but when the local temperature of a water system is too high, the linear polyaspartic acid is easy to break bonds and lose effective functional groups, so that the scale inhibition activity is obviously lost, and therefore, the polyaspartic acid scale inhibitor has the defect of poor thermal stability. In order to improve the thermal stability of polyaspartic acid, chemical modification can be carried out to improve the temperature resistance of polyaspartic acid. In the prior inventions (CN 105645606A: a preparation method of a special scale inhibitor for a heat supply network; CN 102515373A: a green corrosion and scale inhibitor for a hot water boiler; and CN 108726693A: a high-temperature corrosion and scale inhibitor for a heating hot water pipe network in winter and a preparation method thereof), a use method of the polyaspartic acid scale inhibitor applied to a high-temperature system is tried. However, in these patents, polyaspartic acid and other compounds are physically compounded, which is cumbersome in practical use.
Disclosure of Invention
In order to overcome the defect of poor thermal stability of the existing polyaspartic acid scale inhibitor, the invention aims to provide a high-temperature-resistant modified polyaspartic acid scale inhibitor and a preparation method and a use method thereof.
In order to achieve the purpose, the invention adopts the following technical scheme to realize the purpose:
the invention discloses a preparation method of a high-temperature-resistant modified polyaspartic acid scale inhibitor, which comprises the following steps:
maleic anhydride and urea are used as raw materials and react in a mixed acid solution to obtain polysuccinimide;
the polysuccinimide and prolinamide are subjected to ring-opening grafting reaction to prepare the high-temperature-resistant modified polyaspartic acid scale inhibitor.
Preferably, the preparation method of the high-temperature-resistant modified polyaspartic acid scale inhibitor is characterized by comprising the following steps of:
1) preparation of ammonium hydrogen maleate
Fully dissolving maleic anhydride in water to prepare a maleic anhydride aqueous solution, adding urea powder into the maleic anhydride aqueous solution, and generating ammonium hydrogen maleate through a ring-opening reaction;
2) preparation of polysuccinimide
Under the reflux condition, heating the reaction solution containing ammonium hydrogen maleate in the step 1) to 160 +/-5 ℃, then adding the mixed acid solution, heating to 180 +/-5 ℃, and reacting for 1.5-3 h to obtain polysuccinimide;
3) preparation of modified polyaspartic acid
Under the condition of water bath at 40-60 ℃, polysuccinimide and prolinamide are subjected to ring opening grafting reaction in water, alkali liquor is added to open the ring of the part which is not grafted in a polysuccinimide chain segment, after the reaction is carried out for 12-24 ℃, the pH value of a reaction system is adjusted to be neutral, and a product is precipitated by alcohol and dried to prepare modified polyaspartic acid, namely the high-temperature-resistant modified polyaspartic acid scale inhibitor.
Further, in step 1), an aqueous ammonium hydrogen maleate solution is prepared: adding maleic anhydride and deionized water into a three-neck flask with a condensing device, and magnetically stirring in an oil bath kettle to fully dissolve. Uniformly adding urea powder into maleic anhydride aqueous solution to react, and in the process, maleic anhydride and ammonia donor urea are subjected to ring-opening reaction to generate ammonium hydrogen maleate.
Preferably, in the step 1), the temperature for dissolving the maleic anhydride is 60-80 ℃, and the molar ratio of the maleic anhydride to the urea is 1: 0.5-1: 0.7, and the temperature of the ring-opening reaction is 80-110 ℃.
Further, in step 2), Polysuccinimide (PSI) synthesis: introducing cold water of 5 ℃ into a condensation pipe for condensation and reflux, raising the temperature of the generated ammonium hydrogen maleate solution to 160 +/-5 ℃, and adding mixed acid of sulfuric acid and phosphoric acid into the system. Then heating to 180 +/-5 ℃ for continuous reaction, and polymerizing the ammonium hydrogen maleate monomer to generate orange-red polysuccinimide.
Further, in step 3), modification of polyaspartic acid: performing ring opening grafting on polysuccinimide and goose yellow prolinamide in deionized water in a water bath at 40-60 ℃, then adding sodium hydroxide alkali liquor to perform ring opening on the part which is not grafted in the polysuccinimide chain segment, adjusting the pH value to be neutral after reacting for a period of time, separating out by using absolute ethyl alcohol, separating and drying to obtain light yellow brittle solid cyclic micromolecule modified polyaspartic acid (PASP-Pro).
In addition, similarly, polyaspartic acid synthesis can employ: hydrolyzing and ring-opening polysuccinimide in sodium hydroxide alkali liquor in a water bath environment at 40-60 ℃ to obtain polyaspartic acid, and then separating out the polyaspartic acid by using absolute ethyl alcohol. Separating and drying to obtain light yellow viscous Polyaspartic Acid (PASP).
Preferably, in the step 2), the mixed acid solution is added to the reaction kettle and is prepared from sulfuric acid and phosphoric acid according to the volume ratio of 1: 1. More preferably, the dosage of the mixed acid of the sulfuric acid and the phosphoric acid is 1.6-2 mL.
Preferably, in step 3), the molar ratio of polysuccinimide to prolinamide is 1: 0.5-1: 0.75; the open-loop grafting reaction time is 4-8 h.
Preferably, in the step 3), the alkali liquor used for hydrolysis and conference opening adopts a sodium hydroxide solution with the concentration of 2.5-3 mol/L, wherein the volume of the sodium hydroxide solution added per g of polysuccinimide is 5-6 mL.
Preferably, before step 3), an operation of purifying the polysuccinimide prepared in step 2) is further included, specifically including:
taking out the prepared crude polysuccinimide product, drying, completely dissolving the crude polysuccinimide product by adopting N-N-dimethylformamide, filtering, collecting filtrate by adopting absolute ethyl alcohol, filtering, separating by suction after a product is separated out, and drying;
after repeating the purification operation 2 times, the product was ground to obtain purified polysuccinimide.
Specifically, the crude orange-red solid polysuccinimide attached to the wall of the flask was taken out, dried, completely dissolved with N-Dimethylformamide (DMF), poured into a funnel with qualitative analysis filter paper, filtered, and the filtrate was collected in a beaker containing absolute ethanol. Polysuccinimide is precipitated in pink floccule in absolute ethyl alcohol, and is subjected to suction filtration and separation, and the obtained product is placed in a vacuum oven for drying. And repeating the purification step for 2 times, and grinding to obtain the dark red purified polysuccinimide.
Further preferably, the volume ratio of the absolute ethyl alcohol to the N-N-dimethylformamide used for collecting the filtrate is more than 5.
The invention also discloses the high-temperature-resistant modified polyaspartic acid scale inhibitor prepared by the preparation method.
The invention also discloses a use method of the high-temperature-resistant modified polyaspartic acid scale inhibitor, and when the high-temperature-resistant modified polyaspartic acid scale inhibitor is used for water system treatment at the temperature of below 90 ℃, long-acting scale inhibition effect can be maintained;
when the high-temperature-resistant modified polyaspartic acid scale inhibitor is treated in a water system with local temperature reaching 170 ℃, the scale inhibition effect can be maintained for 3.5 h;
when in use, the water system with the pH value of 6.0-8.5 and the calcium ion concentration lower than 700mg/L is suitable;
the concentration of the high-temperature-resistant modified polyaspartic acid scale inhibitor in use is 10-20 mg/L.
Compared with the prior art, the invention has the following beneficial effects:
the preparation method of the high-temperature-resistant modified polyaspartic acid scale inhibitor disclosed by the invention has the advantages that the polysuccinimide precursor is synthesized by using a maleic anhydride method, the synthesis condition is mild, the novel environment-friendly high-temperature-resistant calcium carbonate scale inhibitor is synthesized by using the nitrogen-containing heterocyclic small-molecule prolinamide modified polyaspartic acid, the reaction condition is mild, the reaction raw materials are easy to obtain, and the preparation method is suitable for large-scale production.
The modified polyaspartic acid scale inhibitor prepared by the method is nitrogen-containing heterocyclic small molecule modified polyaspartic acid, belongs to a phosphorus-free environment-friendly scale inhibitor, and is characterized in that in the modification process of polyaspartic acid, a heterocyclic group with a stable structure is selected to perform amidation reaction with polyaspartic acid, and a rigid prolinamide molecule is grafted on linear polyaspartic acid, so that the steric hindrance of the original polyaspartic acid chain is increased, and the chain segment is not easy to move. On the other hand, a new hydrogen bond is generated, which is beneficial to maintaining the stable structure of the polymer. Under the action, the modified polyaspartic acid scale inhibitor has stable structure at high temperature and maintains high-efficiency scale inhibition effect. The scale inhibitor overcomes the defect of poor scale inhibition effect of the existing polyaspartic acid at high temperature, has excellent scale inhibition performance on a calcium carbonate type scale formation system, and is suitable for water circulation systems with local high temperature in urban geothermal heating systems, oil well exploitation production and the like.
The modified polyaspartic acid scale inhibitor disclosed by the invention plays a scale inhibition role at high temperature, is obviously different from a traditional organic phosphoric acid system, and realizes a green scale inhibition target process, so that the prepared modified polyaspartic acid scale inhibitor can be used in the water fields of industrial circulating water, boiler water, geothermal water, urban heating water, oil field exploitation and the like.
Drawings
FIG. 1 is an infrared spectrum of modified molecular prolinamides (Pro), Polyaspartic Acids (PASP) and modified polyaspartic acids (PASP-Pro);
FIG. 2 is a graph showing the effect of constant temperature water bath temperature on calcium carbonate scale inhibition performance of aspartic acid (PASP) and modified polyaspartic acid (PASP-Pro);
FIG. 3 is a graph showing the effect of Polyaspartic Acid (PASP) and modified polyaspartic acid (PASP-Pro) on the scale inhibition performance of calcium carbonate scale at different constant temperature durations;
FIG. 4 is a graph showing the effect of different pretreatment temperatures on calcium carbonate scale inhibition performance of Polyaspartic Acid (PASP) and modified polyaspartic acid (PASP-Pro);
FIG. 5 shows Ca in solution2+Concentration of Polyaspartic Acid (PASP) and modified Polyaspartic Acid (PA)SP-Pro) on calcium carbonate scale inhibition performance of calcium carbonate scale.
Detailed Description
In order to make the technical solutions of the present invention better understood, the technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
It should be noted that the terms "first," "second," and the like in the description and claims of the present invention and in the drawings described above are used for distinguishing between similar elements and not necessarily for describing a particular sequential or chronological order. It is to be understood that the data so used is interchangeable under appropriate circumstances such that the embodiments of the invention described herein are capable of operation in sequences other than those illustrated or described herein. Furthermore, the terms "comprises," "comprising," and "having," and any variations thereof, are intended to cover a non-exclusive inclusion, such that a process, method, system, article, or apparatus that comprises a list of steps or elements is not necessarily limited to those steps or elements expressly listed, but may include other steps or elements not expressly listed or inherent to such process, method, article, or apparatus.
The invention is described in further detail below with reference to the accompanying drawings:
the invention discloses a preparation method of a high-temperature-resistant polyaspartic acid scale inhibitor synthesized by modifying nitrogen-containing heterocyclic micromolecules, which comprises the following steps:
(A) preparation of Polysuccinimide (PSI) by maleic anhydride method
And adding 20-30 g of maleic anhydride solid and 20-30 ml of deionized water into a 500ml three-neck flask with a condensing device, magnetically stirring, controlling the temperature of an oil bath to be 80 +/-5 ℃, and heating for 60-90 min to completely dissolve the maleic anhydride.
Controlling the molar ratio of the maleic anhydride to the urea to be 1: 0.5-1: 0.7, uniformly adding urea powder into the obtained homogeneous maleic anhydride solution, controlling the temperature of an oil bath to be 80 +/-5 ℃, and heating for 60-90 min to ensure that the maleic anhydride and the ammonia donor urea fully generate ammonium hydrogen maleate through a ring-opening reaction.
And (3) introducing cold water with the temperature of 5 ℃ into a condensation pipe of the three-neck flask to start condensation, continuously heating to 160 +/-5 ℃, keeping for a period of time, boiling the colorless ammonium hydrogen maleate solution and gradually becoming turbid, and finding that a small amount of orange solid is generated on the wall of the three-neck flask. Slowly adding (paying attention to the dropping speed to prevent the bumping) 1.6-2 ml of phosphoric acid and sulfuric acid into a three-neck flask, wherein the volume ratio of the phosphoric acid to the sulfuric acid is 1: the mixed acid solution of 1 is used as a dehydrating agent to promote the polymerization reaction, and then the mixed acid is added, the temperature is raised to 180 +/-5 ℃, and the reaction is maintained for 1.5-3 hours.
(B) Purified Polysuccinimide (PSI)
Taking out the orange-red polysuccinimide solid obtained in the step (A), drying, adding 20ml of N-N-Dimethylformamide (DMF), dissolving into an orange-red solution, filtering by using No. 102 qualitative filter paper, and collecting the filtrate by using absolute ethyl alcohol, wherein the volume of the used ethyl alcohol is at least more than 100 ml. Polysuccinimide is precipitated in the form of pink flocculent precipitate at the bottom of absolute ethyl alcohol, and the obtained pink filter cake is put in a vacuum drying oven for complete drying at 60-80 ℃ after being subjected to suction filtration and separation.
And repeating the steps for 2 times, and drying and grinding the obtained product to obtain the dark red precursor polysuccinimide.
(C) Preparation of Polyaspartic Acid (PASP) and modified polyaspartic acid (PASP-Pro)
(C1) In a water bath environment at 60 ℃, 2g of the polysuccinimide powder purified in the step (B) is placed in 10ml of 2.5mol/L sodium hydroxide alkali liquor for hydrolysis ring opening, the orange polysuccinimide solution gradually becomes light yellow, and after hydrolysis time is 12-24 hours, the polyaspartic acid solution with proper molecular weight is obtained. Adding appropriate amount of hydrochloric acid to adjust pH to neutral, dripping anhydrous ethanol with volume more than 50ml, and precipitating polyaspartic acid at the bottom of the anhydrous ethanol to obtain yellowish mucus. Separating and drying to obtain the light yellow viscous polyaspartic acid.
(C2) In a water bath at 60 ℃, 2g of the polysuccinimide powder purified in the step (B) is completely dissolved in 10ml of deionized water, 1.2-1.8 g of the goose yellow prolinamide powder is slowly added to the polysuccinimide powder for ring-opening grafting, after reaction for 4-8 h, 5ml of 2.5mol/L sodium hydroxide alkali liquor is added, the part of the polysuccinimide chain segment which is not grafted with the monomer is hydrolyzed and subjected to ring-opening in an alkaline environment, after reaction for 12-18 h, a proper amount of hydrochloric acid is added to adjust the pH value to be neutral, then anhydrous ethanol with the volume of more than 75ml is added dropwise, modified polyaspartic acid is separated out at the bottom of the anhydrous ethanol, and after separation and drying, light yellow brittle solid cyclic micromolecular modified polyaspartic acid is obtained.
Example 1 (prolinamide-modified polyaspartic acid)
Step 1: 20g of maleic anhydride and 20ml of distilled water were placed in a 250ml three-necked round-bottomed flask with a condenser and dissolved by magnetic stirring for 1 hour under an oil bath at 80 ℃. 9g of urea powder was slowly added to the solution and stirred magnetically for 1h until well mixed. After the experiment started, 5 ℃ condensed water was switched on, the oil bath temperature was raised to 160 ℃, and then the mixture was added in a volume ratio of 1:1, 2ml of mixed acid of sulfuric acid and phosphoric acid, continuously heating to 180 ℃, and continuously reacting for 3 hours to generate orange red Polysuccinimide Solid (PSI) on the inner wall surface of the beaker.
Step 2: and (2) taking the orange-red polysuccinimide solid obtained in the step (1) out, drying, adding 20ml of N-N-dimethylformamide to dissolve the orange-red polysuccinimide solid into an orange-red solution, filtering, and collecting filtrate by using enough absolute ethyl alcohol. Filtering and separating pink flocculent precipitate separated out from the absolute ethyl alcohol, and drying the obtained filter cake in a vacuum oven at the temperature of 80 ℃ for 24 hours.
The purification step was repeated 2 times and ground to give a dark red polysuccinimide powder.
And step 3: and (2) completely dissolving 2g of the purified polysuccinimide powder obtained in the step (2) in 10ml of deionized water in a water bath at 60 ℃, adding 1.5g of prolinamide powder, and carrying out ring-opening grafting reaction for 4-8 h. Adding 5ml of 2.5mol/L sodium hydroxide alkali liquor, carrying out hydrolysis reaction for 12-18 h, adjusting the pH to be neutral by using hydrochloric acid, dripping into 100ml of absolute ethyl alcohol, separating and drying precipitated precipitate, and purifying for 1-2 times to obtain the prolinamide modified polyaspartic acid.
The infrared spectrum of the prolinamide modified polyaspartic acid obtained is shown in FIG. 1. The infrared spectra of the modified molecules prolinamide (Pro), Polyaspartic Acid (PASP) and modified polyaspartic acid (PASP-Pro) are included in fig. 1.
Comparative example 1 (polyaspartic acid)
And step 3: and (2) in a water bath at 60 ℃, hydrolyzing and ring-opening 2g of the purified polysuccinimide powder obtained in the step (2) in 10ml of 2.5mol/L sodium hydroxide alkali liquor for 24h, adjusting the pH to be neutral by using hydrochloric acid, dripping into 100ml of absolute ethyl alcohol, separating and drying the separated precipitate, and purifying for 1-2 times to obtain the polyaspartic acid. The prepared polyaspartic acid was prepared as a dilute solution with ultrapure water.
COMPARATIVE EXAMPLE 2 (blank group)
An equal volume of ultrapure water was used as a blank for the scale inhibitor solution.
And (3) testing the scale inhibition performance: and (3) carrying out scale inhibition performance test on polyaspartic acid and prolinamide modified polyaspartic acid according to a calcium carbonate deposition method for measuring scale inhibition performance of GB/T166322008 water treatment agents.
Preparing a test solution: adding 100ml of calcium chloride solution into a 250ml volumetric flask to ensure that the addition of calcium ions is 60 mg; adding a certain volume of scale inhibitor solution by a pipette, wherein the adding amount of the polyaspartic acid or the prolinamide modified polyaspartic acid is 5mg, and shaking up; then 100ml of sodium bicarbonate solution was slowly added to make the amount of bicarbonate ions added 183mg, and ultrapure water was supplemented to a volume of 250 ml.
Application experiment one: taking 15 250ml round-bottom flasks numbered 1-15, and accurately adding Ca into the flasks 1-15 according to the preparation steps of the test solution2+Concentration of 240mg/L, HCO3 -The concentration is 732mg/L, wherein the prolinamide modified polyaspartic acid prepared in the embodiment 1 of the invention is added into a No. 1-5 flask, and the concentration is 20 mg/L; adding polyaspartic acid prepared in comparative example 1 of the invention into a No. 6-10 flask, wherein the concentration is 20 mg/L; an equal volume of ultrapure water was added to flask 11-15 as a blank control. Adjusting the pH to 7Placing the components in 50, 60, 70, 80, 90 deg.C constant temperature water bath kettle respectively, water bath time is 10 hr, cooling the test solution to room temperature after experiment, collecting the filtrate, and testing Ca by ion chromatography2+And (4) calculating the scale inhibition rate. The results of the measurements are shown in Table 1 and are plotted in FIG. 2.
Table 1: the duration of the constant temperature water bath is controlled to be 10 hours, and the constant temperature affects the calcium carbonate scale resistance of the polyaspartic acid and the modified polyaspartic acid.
TABLE 1
| Example 1 | 1(50℃) | 2(60℃) | 3(70℃) | 4(80℃) | 5(90℃) |
| Scale inhibition rate | 96.0 | 94.1 | 95.6 | 95.3 | 88.2 |
| Comparative example 1 | 6(50℃) | 7(60℃) | 8(70℃) | 9(80℃) | 10(90℃) |
| Scale inhibition rate | 94.1 | 93.0 | 96.1 | 92.2 | 86.9 |
From the results of table 1 and fig. 2, it can be seen that: when the water bath temperature of the static experiment is lower, the scale inhibition effect difference of the polyaspartic acid and the modified polyaspartic acid is not large, and when the water bath temperature is higher, the scale inhibition effect of the modified polyaspartic acid is higher than that of the unmodified polyaspartic acid.
Application experiment two: taking 15 250ml round-bottom flasks numbered 1-15, and accurately adding Ca into the flasks 1-15 according to the preparation steps of the test solution2+Concentration of 240mg/L, HCO3 -The concentration is 732mg/L, wherein the prolinamide modified polyaspartic acid prepared in the embodiment 1 of the invention is added into a No. 1-5 flask, and the concentration is 20 mg/L; adding polyaspartic acid prepared in comparative example 1 of the invention into a No. 6-10 flask, wherein the concentration is 20 mg/L; an equal volume of ultrapure water was added to flask 11-15 as a blank control. Adjusting pH to 7, placing the above components in 80 deg.C constant temperature water bath for 6, 8, 10, 15, and 20 hr, cooling the test solution to room temperature, collecting the filtrate, and testing Ca by ion chromatography2+And (4) calculating the scale inhibition rate. The results of the measurements are shown in Table 2 and are plotted in FIG. 3.
Table 2: the temperature of the constant-temperature water bath is controlled to be 80 ℃, and the influence of different constant-temperature time lengths on the calcium carbonate scale resistance of the polyaspartic acid and the modified polyaspartic acid is avoided.
TABLE 2
| Example 1 | 1(6h) | 2(8h) | 3(10h) | 4(15h) | 5(20h) |
| Scale inhibition rate | 93.9 | 95.3 | 97.3 | 96.9 | 85.2 |
| Comparative example 1 | 6(6h) | 7(8h) | 8(10h) | 9(15h) | 10(20h) |
| Scale inhibition rate | 94.1 | 92.2 | 94.6 | 84.7 | 74.4 |
From the results of table 2 and fig. 3, it can be seen that: when the water bath temperature is controlled to be 80 ℃, the scale inhibition effect of the polyaspartic acid and the modified polyaspartic acid is reduced along with the prolonging of the water bath time, but the scale inhibition effect of the modified polyaspartic acid at the same time is obviously higher than that of the modified polyaspartic acid at the same time.
Application experiment three: and (3) marking 8 hydrothermal kettles by 1-8, adding the prolinamide modified polyaspartic acid solution prepared in the example 1 into No. 1-4 hydrothermal kettles, adding the polyaspartic acid prepared in the comparative example 1 into No. 5-8 hydrothermal kettles, respectively placing the hydrothermally modified polyaspartic acid solutions in high-temperature drying ovens at 110 ℃, 130 ℃, 150 ℃ and 170 ℃ for pretreatment for 3.5 hours, and then taking out and cooling to room temperature. Taking 9 250ml round-bottom flasks numbered 1-9, and accurately adding Ca into the flasks 1-9 according to the preparation steps of the test solution2+Concentration of 240mg/L, HCO3 -The concentration is 732mg/L, wherein pretreated prolinamide modified polyaspartic acid is added into a No. 1-4 flask, and the concentration is 20 mg/L; adding the polyaspartic acid prepared in comparative example 1 into a No. 5-8 flask, wherein the concentration is 20 mg/L; an equal volume of ultrapure water was added to flask 9 as a blank control. Adjusting pH to 7, placing the above components in 80 deg.C constant temperature water bath for 10 hr, cooling the test solution to room temperature, filtering, and measuring Ca content in the filtrate by ion chromatography2+And (4) calculating the scale inhibition rate. The results of the measurements are shown in Table 3 and plotted in FIG. 4. Table 3: after high-temperature pretreatment for 3.5h, carrying out constant-temperature water bath at 80 ℃ for 10h, wherein the pretreatment temperature has influence on the calcium carbonate scale resistance of the polyaspartic acid and the modified polyaspartic acid.
TABLE 3
| Example 1 | 1(110℃) | 2(130℃) | 3(150℃) | 4(170℃) |
| Scale inhibition rate | 94.6 | 90.8 | 87.1 | 61.7 |
| Comparative example 1 | 5(110℃) | 6(130℃) | 7(150℃) | 8(170℃) |
| Scale inhibition rate | 85.7 | 82.1 | 73.6 | 43.0 |
From the results of table 3 and fig. 4, it can be seen that: along with the increase of the pretreatment temperature, the scale inhibition effect of the polyaspartic acid and the modified polyaspartic acid is reduced in a static test, but the scale inhibition effect of the modified polyaspartic acid is obviously higher than that of the non-modified polyaspartic acid.
Application experiment four: taking 18 250ml round-bottom flasks numbered 1-18, and controlling Ca in the flasks 1-6, 7-12 and 13-18 according to the preparation steps of the test solution2+The concentrations of the proline modified polyaspartic acid are respectively 120, 240, 360, 480, 600 and 720mg/L, and the proline modified polyaspartic acid prepared in the embodiment 1 of the invention is added into a No. 1-6 flask, and the concentration is 20 mg/L; adding polyaspartic acid prepared in comparative example 1 of the invention into a No. 7-12 flask, wherein the concentration is 20 mg/L; an equal volume of ultrapure water was added to flask 13-18 as a blank control. Accurately adding HCO into No. 1-18 flask3 -The concentration is 732mg/L, the pH is adjusted to be 7, each group is placed in a water bath kettle with the constant temperature of 80 ℃, the water bath time is 10h, and the experiment is carried outCooling the sample solution to room temperature after the reaction is finished, and measuring Ca in the filtered filtrate by adopting ion chromatography2+And (4) calculating the scale inhibition rate. The results of the measurements are shown in Table 4 and are plotted in FIG. 5.
Table 4: controlling the duration of the constant-temperature water bath to be 10h and Ca in the solution2+Effect of concentration on calcium carbonate Scale inhibition Properties of the polyaspartic acid and modified polyaspartic acid of the present invention
TABLE 4
| Example 1 | 1(120) | 2(240) | 3(360) | 4(480) | 5(600) | 6(720) |
| Scale inhibition rate | 95.2 | 95.3 | 93.2 | 79.3 | 77.1 | 70.2 |
| Comparative example 1 | 7(120) | 8(240) | 9(360) | 10(480) | 11(600) | 12(720) |
| Scale inhibition rate | 96.4 | 92.2 | 94.7 | 81.9 | 80.7 | 74.6 |
From the results of table 4 and fig. 5, it can be seen that: along with the increase of the concentration of calcium ions in the solution, the scale inhibition effect of the polyaspartic acid and the modified polyaspartic acid is slowly reduced, and the scale inhibition effect of the modified polyaspartic acid is slightly lower than that of unmodified polyaspartic acid, but the overall effect is similar.
The above are only the specific examples and comparative examples of the present invention, and the results of the specific embodiments show that, after high-temperature pretreatment in a water bath with temperature change and constant temperature for a long time, the scale inhibition effect of the proline-modified polyaspartic acid prepared in the examples on calcium carbonate is obviously higher than that of the unmodified polyaspartic acid in the comparative examples, which shows that the proline-modified polyaspartic acid obviously improves the high-temperature scale inhibition performance of polyaspartic acid on calcium carbonate systems. In addition, under the conditions of high mineralization and high calcium water quality, the proline amide modified polyaspartic acid shows the scale inhibition performance similar to that of the polyaspartic acid, and the proline amide modified polyaspartic acid can stably play the role of calcium carbonate scale inhibition in a high mineralization and high calcium water system.
The above-mentioned contents are only for illustrating the technical idea of the present invention, and the protection scope of the present invention is not limited thereby, and any modification made on the basis of the technical idea of the present invention falls within the protection scope of the claims of the present invention.
Claims (10)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202110287663.6A CN113087903B (en) | 2021-03-17 | 2021-03-17 | High-temperature-resistant modified polyaspartic acid scale inhibitor and preparation method and use method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202110287663.6A CN113087903B (en) | 2021-03-17 | 2021-03-17 | High-temperature-resistant modified polyaspartic acid scale inhibitor and preparation method and use method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN113087903A true CN113087903A (en) | 2021-07-09 |
| CN113087903B CN113087903B (en) | 2022-05-20 |
Family
ID=76668429
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202110287663.6A Active CN113087903B (en) | 2021-03-17 | 2021-03-17 | High-temperature-resistant modified polyaspartic acid scale inhibitor and preparation method and use method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN113087903B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115140852A (en) * | 2022-07-25 | 2022-10-04 | 天津大学 | Scale inhibitor for inhibiting generation of calcium carbonate scale in geothermal fluid on inner wall of geothermal wellbore |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1121933A (en) * | 1994-07-21 | 1996-05-08 | 拜尔公司 | A process for the production of polysuccinimide or maleic amide acid |
| CN1123252A (en) * | 1994-09-12 | 1996-05-29 | 罗姆和哈斯公司 | Method of inhibiting sulfate scale in aqueous systems using poly(amino acids) |
| US5750070A (en) * | 1996-07-19 | 1998-05-12 | Nalco Chemical Company | Use of biodegradable polymers in preventing corrosion and scale build-up |
| US5776875A (en) * | 1996-07-16 | 1998-07-07 | Nalco Chemical Company | Use of biodegradable polymers in preventing scale build-up |
| CN1629207A (en) * | 2003-11-03 | 2005-06-22 | 福利亚有限公司 | Methods of synthesis of polysuccinimide, copolymers of polysuccinimide and derivatives thereof |
| CN107619117A (en) * | 2016-07-13 | 2018-01-23 | 中国石油化工股份有限公司 | Non-phosphate inhibitor and its preparation method and application and water treatment composition and its application |
| CN109369913A (en) * | 2018-09-13 | 2019-02-22 | 天津大学 | PH-responsive polyaspartic acid grafted with hydrophobic amino acid and preparation method thereof |
| CN110028667A (en) * | 2019-04-22 | 2019-07-19 | 苏州美瑞姿生物科技有限公司 | A kind of synthetic method for the poly-aspartate derivant that niacinamide is modified |
| CN111333840A (en) * | 2020-04-06 | 2020-06-26 | 刘云晖 | Amino acid polymer with intrinsic self-repairing property and preparation method thereof |
-
2021
- 2021-03-17 CN CN202110287663.6A patent/CN113087903B/en active Active
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1121933A (en) * | 1994-07-21 | 1996-05-08 | 拜尔公司 | A process for the production of polysuccinimide or maleic amide acid |
| CN1123252A (en) * | 1994-09-12 | 1996-05-29 | 罗姆和哈斯公司 | Method of inhibiting sulfate scale in aqueous systems using poly(amino acids) |
| US5776875A (en) * | 1996-07-16 | 1998-07-07 | Nalco Chemical Company | Use of biodegradable polymers in preventing scale build-up |
| US5750070A (en) * | 1996-07-19 | 1998-05-12 | Nalco Chemical Company | Use of biodegradable polymers in preventing corrosion and scale build-up |
| CN1629207A (en) * | 2003-11-03 | 2005-06-22 | 福利亚有限公司 | Methods of synthesis of polysuccinimide, copolymers of polysuccinimide and derivatives thereof |
| CN107619117A (en) * | 2016-07-13 | 2018-01-23 | 中国石油化工股份有限公司 | Non-phosphate inhibitor and its preparation method and application and water treatment composition and its application |
| CN109369913A (en) * | 2018-09-13 | 2019-02-22 | 天津大学 | PH-responsive polyaspartic acid grafted with hydrophobic amino acid and preparation method thereof |
| CN110028667A (en) * | 2019-04-22 | 2019-07-19 | 苏州美瑞姿生物科技有限公司 | A kind of synthetic method for the poly-aspartate derivant that niacinamide is modified |
| CN111333840A (en) * | 2020-04-06 | 2020-06-26 | 刘云晖 | Amino acid polymer with intrinsic self-repairing property and preparation method thereof |
Non-Patent Citations (1)
| Title |
|---|
| 吕小改: "聚天冬氨酸/对氨基苯甲酰胺接枝物的合成及阻垢性能", 《化学研究》 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115140852A (en) * | 2022-07-25 | 2022-10-04 | 天津大学 | Scale inhibitor for inhibiting generation of calcium carbonate scale in geothermal fluid on inner wall of geothermal wellbore |
| CN115140852B (en) * | 2022-07-25 | 2023-11-28 | 天津大学 | A scale inhibitor that inhibits the generation of calcium carbonate scale in geothermal fluid on the inner wall of geothermal wellbore |
Also Published As
| Publication number | Publication date |
|---|---|
| CN113087903B (en) | 2022-05-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN103265696B (en) | Dendrimer with pentaerythritol core terminal and phosphonic acid terminal group, preparation method and uses thereof | |
| CN100551933C (en) | A method for extracting bacterial alginate | |
| CN102875808B (en) | Polyaspartic acid derivate, as well as preparation method and application thereof | |
| CN102030399B (en) | Hyperbranched polymer flocculant for treating waste drilling fluid and preparation method thereof | |
| CN105482117B (en) | Poly-aspartate/urea graft copolymer and its preparation method and application | |
| CN102952266A (en) | Separation and purification method of gamma-polyglutamic acid | |
| CN102963983B (en) | Vertical flow artificial wetland substrate modified based on LDHs (layered double hydroxides) coating film and preparation method of substrate | |
| CN113087903A (en) | High-temperature-resistant modified polyaspartic acid scale inhibitor and preparation method and use method thereof | |
| CN105032195A (en) | Scale inhibitor for reverse osmosis membrane and preparation method of scale inhibitor | |
| CN104530428A (en) | Preparation method of modified polyaspartic acid copolymer | |
| CN106748855B (en) | A kind of fumaropimaric acid modified propylene amide compound, preparation method and its prepared polymer | |
| CN103073100A (en) | Dextrin-modified polysilicon ferric sulfate composite flocculating agent and preparation method thereof | |
| CN111072122B (en) | Composite heavy metal chelating agent containing dithio carboxylate functionalized ethoxylated pentaerythritol core hyperbranched polymer | |
| CN110683623B (en) | Preparation method of tannin and aluminum salt modified decolorant | |
| CN110305325B (en) | Humic acid polyethylene glycol graft copolymer and preparation method thereof | |
| CN106698673A (en) | Laccase and modified dicyandiamide formaldehyde composite decolorant | |
| CN112456659A (en) | A kind of scale inhibitor and its preparation method and application | |
| CN101913792B (en) | A kind of method of bamboo tar crude phenol modified sulfamic acid series superplasticizer | |
| CN117362519A (en) | Sewage flocculant and preparation method and application thereof | |
| CN103979660B (en) | A method for preparing lignin-based cationic organic flocculant from papermaking sludge | |
| CN109437415A (en) | Without phosphorus reverse osmosis antisludging agent PER-PAMAM and preparation method thereof | |
| CN108862642A (en) | The preparation method of modified polyaspartic acid scale inhibitor | |
| CN104387585A (en) | Aspartic acid-lysine copolymer and synthetic method thereof | |
| CN109081552B (en) | A kind of preparation method of inorganic-organic composite sludge conditioner and its application | |
| CN104860386B (en) | A kind of efficient dephosphorization agent |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |