TWI742920B - Melamine-formaldehyde resin composition and its product - Google Patents

Abstract

Provided is a melamine-formaldehyde resin composition. The melamine-formaldehyde resin composition comprises 2,4,6-tri[bis(methoxymethyl)amino]-1,3,5-triazine, wherein the melamine-formaldehyde resin composition is analyzed by Liquid Chromatography-Mass Spectrometry, obtaining that based on the total area of all chromatographic peaks in the melamine-formaldehyde resin composition, the area of the chromatographic peak of 2,4,6-tri[bis(methoxymethyl)amino]-1,3,5-triazine ranges from 15% to 33%. The melamine-formaldehyde resin composition of the present invention has superior freeze resistance and extended storage life.

Description

Melamine formaldehyde resin composition and its products

This creation is about a resin composition and its products, especially a melamine-formaldehyde resin composition and products containing the melamine-formaldehyde resin composition.

Melamine-formaldehyde resin (MF) is a synthetic resin produced by the addition reaction of melamine and formaldehyde. It has good flame retardancy, heat resistance, water resistance, solvent resistance, insulation, and Because of its high hardness, it is often used in the manufacture of fire-resistant building materials, fabrics, plastics, metal plates, coatings and other daily life products. Common melamine tableware is made of melamine formaldehyde resin.

However, the properties of the melamine formaldehyde resin produced by the aforementioned method are easily affected by the external environmental temperature. When the ambient temperature is lower, the viscosity of the melamine formaldehyde resin is higher. In addition, the existing melamine formaldehyde resin is prone to freezing at a lower ambient temperature. This phenomenon not only greatly shortens the storage period of the melamine formaldehyde resin, but also affects the resin Manufacturers and processing industries cause a lot of inconvenience, and also limit its operability and processability.

In view of the problems of the existing melamine formaldehyde resins that are easy to freeze at low temperatures and insufficient storage period, there is a great need to develop a melamine formaldehyde resin with excellent freezing resistance to solve the problem that the existing melamine formaldehyde resins are prone to freezing in a low temperature environment. The inconvenience and usage restrictions come.

In view of this, the purpose of this creation is to extend the low-temperature storage period of the melamine-formaldehyde resin composition and improve the frost resistance of the melamine-formaldehyde resin composition.

To achieve the foregoing objective, the first aspect of the present creation provides a melamine-formaldehyde resin composition comprising at least one melamine oligomer. The melamine-formaldehyde resin composition is combined with liquid chromatography-mass spectrometry (LC). -MS) analysis, the mass-to-charge ratio (m/z) of the at least one melamine oligomer can be 393 to 692, and the total area of all the chromatographic peaks in the melamine formaldehyde resin composition is As a benchmark, the total area of the chromatographic peaks with a mass-to-charge ratio of 393 to 692 can be 2% to 20%.

According to the technical means of the first aspect of this creation, by appropriately adjusting the ratio of the chromatographic peak area with a mass-to-charge ratio of 393 to 692 in the LC-MS results of the melamine formaldehyde resin composition to the total area of all chromatographic peaks, this creation The melamine-formaldehyde resin composition can have excellent frost resistance, and the melamine-formaldehyde resin composition can be stored in a low-temperature environment for a long time without forming crystals, that is, the low-temperature storage period of the melamine-formaldehyde resin composition is prolonged. According to this, the technical means of the first aspect of this creation can solve the inconvenience and use restrictions caused by the freezing of the melamine formaldehyde resin in the low temperature environment in the past.

According to the technical means of the first aspect of this creation, in one of the implementation aspects, the total area of all the chromatographic peaks in the melamine formaldehyde resin composition is used as a reference, and the mass-to-charge ratio is the sum of the areas of the chromatographic peaks of 393 to 692 It can be 2% to 19%, 2% to 18%, or 5% to 15%. Preferably, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 393 to 692 can be 7% to 20%, thereby making the melamine formaldehyde The resin composition has a longer low-temperature storage period and better frost resistance.

式(I)； 其中，a可為2至6的整數，b可為1至6的整數，且R₁ 及R₂ 可各自獨立為羥基或甲氧基。所述a和b可為相同或不同的整數。According to the technical means of the first aspect of this creation, the at least one melamine oligomer has the structure shown in the following formula (I):

Formula (I); Wherein, a can be an integer from 2 to 6, b can be an integer from 1 to 6, and R ₁ and R ₂ can each independently be a hydroxyl group or a methoxy group. The a and b may be the same or different integers.

式(II)； 式(III)；    

式(IV)； 式(V)。 For example, the at least one melamine oligomer may have a structure shown in at least one of the following formula (II) to formula (V):

Formula (II); Formula (III);

Formula (IV); 式(V).

、

、

、

、

、

、

、或

，但並非僅限於此。 In other embodiments, in addition to the structures shown in the aforementioned formulas (II) to (V), the at least one melamine oligomer may also have the structure shown below:

,

,

,

,

,

,

,or

, But not limited to this.

For the melamine oligomers represented by the structures shown in the above formula (II) to formula (V) and/or the eight structures listed in other embodiments, the mass-to-charge ratio of the melamine oligomer can fall between 393 and 692 Within the range, the melamine oligomer may have an asymmetric structure. In some embodiments, the a and b may be different integers.

According to the technical means of the first aspect of the present creation, preferably, the mass-to-charge ratio of the at least one melamine oligomer may be 393 to 452, and it may have the structure shown in the above formula (II) to formula (V). In one embodiment, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the sum of the areas of the chromatographic peaks with a mass-to-charge ratio of 393 to 452 may be 5% to 15%, 5% To 12%, or 5% to 10%. Preferably, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 393 to 452 can be 7% to 12%, thereby making the melamine formaldehyde The resin composition has a longer low-temperature storage period and better frost resistance.

In some embodiments, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 393 to 452 may be 5% to 8%. In some embodiments, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 393 to 452 may be 8.2% to 12%, and further It can be 8.4% to 12%.

式(VI)； 其中該式(VI)所示之成分的質荷比可為300至310，以該三聚氰胺甲醛樹脂組合物中全部的層析峰之總面積為基準，該質荷比為300至310的層析峰之面積的總和可為1.15%至2.50%。於其中一實施態樣，以該三聚氰胺甲醛樹脂組合物中全部的層析峰之總面積為基準，該質荷比為300至310的層析峰之面積的總和可為1.15%至2.40%；於另一實施態樣，以該三聚氰胺甲醛樹脂組合物中全部的層析峰之總面積為基準，該質荷比為300至310的層析峰之面積的總和可為1.15%至2.20%。According to the technical means of the first aspect of this creation, in addition to the aforementioned at least one melamine oligomer, the melamine-formaldehyde resin composition may further include the following components represented by formula (VI):

Formula (VI); The mass-to-charge ratio of the component represented by the formula (VI) can be 300 to 310, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, and the mass-to-charge ratio is between 300 and 310. The total area can be 1.15% to 2.50%. In one embodiment, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 300 to 310 may be 1.15% to 2.40%; In one embodiment, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 300 to 310 may be 1.15% to 2.20%.

式(VII)； 其中該式(VII)所示之成分的質荷比可為330至340；以該三聚氰胺甲醛樹脂組合物中全部的層析峰之總面積為基準，該質荷比為300至310的層析峰之面積與該質荷比為330至340的層析峰之面積的總和可為1.8%至5.0%，進一步可為1.8%至4.8%。較佳地，以該三聚氰胺甲醛樹脂組合物中全部的層析峰之總面積為基準，該質荷比為300至310的層析峰之面積與該質荷比為330至340的層析峰之面積的總和可落在1.80%至1.97%之範圍或者2.10%至4.60%之範圍，藉此令三聚氰胺甲醛樹脂組合物具有更長的低溫儲存期和更佳的抗凍性。According to the technical means of the first aspect of this creation, in addition to the aforementioned at least one melamine oligomer, the melamine-formaldehyde resin composition further includes the following components represented by formula (VII):

Formula (VII); The mass-to-charge ratio of the component represented by the formula (VII) can be 330 to 340; based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the mass-to-charge ratio is between 300 and 310. The sum of the area and the area of the chromatographic peak having a mass-to-charge ratio of 330 to 340 may be 1.8% to 5.0%, and further may be 1.8% to 4.8%. Preferably, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the area of the chromatographic peak with a mass-to-charge ratio of 300 to 310 and the area of the chromatographic peak with a mass-to-charge ratio of 330 to 340 The sum can fall within the range of 1.80% to 1.97% or the range of 2.10% to 4.60%, so that the melamine formaldehyde resin composition has a longer low-temperature storage period and better frost resistance.

式(VIII)； 以該三聚氰胺甲醛樹脂組合物中全部的層析峰之總面積為基準，該2,4,6-三[雙(甲氧基甲基)胺基]-1,3,5-三嗪的層析峰之面積可為15%至33%、15%至31%、15%至30%、或15%至28%。According to the technical means of the first aspect of the present creation, in addition to the aforementioned at least one melamine oligomer, the melamine formaldehyde resin composition may also include the following formula (VIII), 2,4,6-tris[bis(methoxy (Methyl)amino]-1,3,5-triazine:

Formula (VIII); Based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl)amino]-1,3,5-triazine The area of the peak can be 15% to 33%, 15% to 31%, 15% to 30%, or 15% to 28%.

In one embodiment, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl)amino]-1,3, The area of the chromatographic peak of 5-triazine may be 20% to 31%. Preferably, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl)amino]-1,3,5-tris The area of the chromatographic peak of oxazine can fall in the range of 20% to 30%, 20% to 29%, 20% to 28%, or 20% to 27%, thereby making the melamine formaldehyde resin composition Has a longer low-temperature storage period and better frost resistance.

In some embodiments, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl)amino]-1,3 The area of the chromatographic peak of 5-triazine can be 20.0% to 27.8%. In some embodiments, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl)amino]-1,3 The area of the chromatographic peak of 5-triazine can be 28.5% to 30.0%.

In order to achieve the foregoing objective, the second aspect of the present creation provides a melamine-formaldehyde resin composition comprising 2,4,6-tris[bis(methoxymethyl)amino]-1, as shown in the above formula (VIII) 3,5-triazine, wherein the melamine-formaldehyde resin composition is analyzed by liquid chromatography combined with mass spectrometry, and the total area of all chromatographic peaks in the melamine-formaldehyde resin composition is used as a reference, and the 2,4,6- The area of the chromatographic peak of tris[bis(methoxymethyl)amino]-1,3,5-triazine may be 15% to 33%.

According to the technical means of the second aspect of this creation, by chromatographic analysis of 2,4,6-tris[bis(methoxymethyl)amino]-1,3,5-triazine in the melamine formaldehyde resin composition The ratio of the peak area to the total area of all chromatographic peaks is controlled within the above range. The melamine formaldehyde resin composition of the present invention can have excellent antifreeze effect. The melamine formaldehyde resin composition can be stored for a long time in a low temperature environment without Crystallization is generated, that is, the low-temperature storage period of the melamine-formaldehyde resin composition is prolonged. According to this, the technical means of the second aspect of this creation can solve the inconvenience and use restrictions caused by the freezing of the melamine formaldehyde resin in the low temperature environment in the past.

According to the technical means of the second aspect of this creation, in one of the implementation aspects, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl) The area of the chromatographic peak of (base)amino]-1,3,5-triazine may be 15% to 31%, 15% to 30%, or 15% to 28%.

In one embodiment, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl)amino]-1,3, The area of the chromatographic peak of 5-triazine may be 20% to 31%. Preferably, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl)amino]-1,3,5-tris The area of the chromatographic peak of oxazine can fall in the range of 20% to 30%, 20% to 29%, 20% to 28%, or 20% to 27%, thereby making the melamine formaldehyde resin composition Has a longer low-temperature storage period and better frost resistance.

In some embodiments, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl)amino]-1,3 The area of the chromatographic peak of 5-triazine can be 20.0% to 27.8%. In some embodiments, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl)amino]-1,3 The area of the chromatographic peak of 5-triazine can be 28.5% to 30.0%.

According to the technical means of the second aspect of the present creation, the melamine formaldehyde resin composition further includes at least one melamine oligomer, which may have the structure shown in the above formula (I). Wherein, a can be an integer from 2 to 6, b can be an integer from 1 to 6, and R ₁ and R ₂ can each independently be a hydroxyl group or a methoxy group. The a and b may be the same or different integers.

As described in the first aspect, the at least one melamine oligomer may have the structure shown in the above formula (II) to formula (V) and/or the eight structures listed in other embodiments, but it is not limited to this . The mass-to-charge ratio of the at least one melamine oligomer is 393 to 692, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the sum of the areas of the chromatographic peaks with the mass-to-charge ratio of 393 to 692 can be It is 2% to 20%, 2% to 19%, 2% to 18%, or 5% to 15%. Preferably, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 393 to 692 can be 7% to 20%, thereby making the melamine formaldehyde The resin composition has a longer low-temperature storage period and better frost resistance.

According to the technical means of the second aspect of the present creation, the mass-to-charge ratio of the at least one melamine oligomer can be 393 to 452. In one embodiment, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the sum of the areas of the chromatographic peaks with a mass-to-charge ratio of 393 to 452 may be 5% to 15%, 5% To 12%, or 5% to 10%. Preferably, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 393 to 452 can be 7% to 12%, thereby making the melamine formaldehyde The resin composition has a longer low-temperature storage period and better frost resistance.

In some embodiments, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 393 to 452 may be 5% to 8%. In some embodiments, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 393 to 452 may be 8.2% to 12%, and further It can be 8.4% to 12%.

According to the technical means of the second aspect of the present creation, the melamine formaldehyde resin composition further includes the component represented by the above formula (VI); wherein the mass-to-charge ratio of the component represented by the formula (VI) can be 300 to 310, and the The total area of all the chromatographic peaks in the melamine formaldehyde resin composition is a reference, and the total area of the chromatographic peaks with a mass-to-charge ratio of 300 to 310 may be 1.15% to 2.50%. In one embodiment, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 300 to 310 may be 1.15% to 2.40%; In one embodiment, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 300 to 310 may be 1.15% to 2.20%.

According to the technical means of the second aspect of the present creation, the melamine formaldehyde resin composition further includes the component represented by the above formula (VII); wherein the mass-to-charge ratio of the component represented by the formula (VII) can be 330 to 340; The total area of all the chromatographic peaks in the melamine formaldehyde resin composition is a reference, and the sum of the area of the chromatographic peak with a mass-to-charge ratio of 300 to 310 and the area of the chromatographic peak with a mass-to-charge ratio of 330 to 340 may be 1.8% to 5.0%, and may further be 1.8% to 4.8%. Preferably, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the area of the chromatographic peak with a mass-to-charge ratio of 300 to 310 and the area of the chromatographic peak with a mass-to-charge ratio of 330 to 340 The sum can fall within the range of 1.80% to 1.97% or the range of 2.10% to 4.60%, so that the melamine formaldehyde resin composition has a longer low-temperature storage period and better frost resistance.

式(IX)； 式(X)。 In the first and second aspects of this creation, the melamine-formaldehyde resin composition may optionally include the following other ingredients in addition to the aforementioned ingredients, but it is not limited to this:

Formula (IX); 式(X).

In this specification, the 2,4,6-tris[bis(methoxymethyl)amino]-1,3,5-triazine refers to a fully etherified melamine-formaldehyde resin (fully etherified melamine-formaldehyde resin). resin), which can also be called fully methylated melamine-formaldehyde resin, which has a symmetrical structure.

In the first and second aspects of the present creation, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the sum of the areas of the chromatographic peaks with a mass-to-charge ratio of 393 to 692 can be any of the following A value, for example: 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19%, 20%, but not limited to this, each of the above specific values can be used as the end value of other numerical ranges.

In the first and second aspects of the present creation, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the sum of the areas of the chromatographic peaks with a mass-to-charge ratio of 393 to 452 can be any of the following A value, for example: 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, but not limited to this, each of the above specific values Can be used as the end value of other numerical ranges.

In the first and second aspects of the present creation, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the sum of the areas of the chromatographic peaks with a mass-to-charge ratio of 300 to 310 can be any of the following A value, for example: 1.15%, 1.16%, 1.17%, 1.18%, 1.19%, 1.20%, 1.21%, 1.22%, 1.23%, 1.24%, 1.25%, 1.26%, 1.27%, 1.28%, 1.29%, 1.30%, 1.31%, 1.32%, 1.33%, 1.34%, 1.35%, 1.36%, 1.37%, 1.38%, 1.39%, 1.40%, 1.41%, 1.42%, 1.43%, 1.44%, 1.45%, 1.46% , 1.47%, 1.48%, 1.49%, 1.50%, 1.51%, 1.52%, 1.53%, 1.54%, 1.55%, 1.56%, 1.57%, 1.58%, 1.59%, 1.60%,..., 1.90%, 1.91% , 1.92%, 1.93%, 1.94%, 1.95%, 1.96%, 1.97%, 1.98%, 1.99%, 2.00%, 2.01%, 2.02%, 2.03%, 2.04%, 2.05%, 2.06%, 2.07%, 2.08 %, 2.09%, 2.10%, 2.11%, 2.12%, 2.13%, 2.14%, 2.15%, 2.16%, 2.17%, 2.18%, 2.19%, 2.20%, 2.21%, 2.22%, 2.23%, 2.24%, 2.25%, 2.26%, 2.27%, 2.28%, 2.29%, 2.30%, 2.31%, 2.32%, 2.33%, 2.34%, 2.35%, 2.36%, 2.37%, 2.38%, 2.39%, 2.40%, 2.41% , 2.42%, 2.43%, 2.44%, 2.45%, 2.46%, 2.47%, 2.48%, 2.49%, 2.50%, but not limited to this, each of the above specific values can be used as the end value of other numerical ranges .

In the first and second aspects of this creation, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the area of the chromatographic peak with a mass-to-charge ratio of 300 to 310 and the mass-to-charge ratio are The sum of the area of the chromatographic peaks from 330 to 340 can be any of the following values, for example: 1.8%, 1.9%, 2.0%, 2.1%, 2.2%, 2.3%, 2.4%, 2.5%, 2.6%, 2.7%, 2.8 %, 2.9%, 3.0%, 3.1%, 3.2%, 3.3%, 3.4%, 3.5%, 3.6%, 3.7%, 3.8%, 3.9%, 4.0%, 4.1%, 4.2%, 4.3%, 4.4%, 4.5%, 4.6%, 4.7%, 4.8%, 4.9%, 5.0%, but not limited to this, each of the above specific values can be used as the end value of other numerical ranges.

In the first and second aspects of this creation, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxymethyl)amino group ] The area of the chromatographic peak of -1,3,5-triazine can be any of the following values, for example: 15%, 16%, 17%, 18%, 19%, 20%, 21%, 22%, 23% , 24%, 25%, 26%, 27%, 28%, 29%, 30%, 31%, 32%, 33%, but not limited to this, each of the above specific values can be used as other numerical ranges Endpoint value.

In the structure of formula (I) described in the first and second aspects of this creation, a can be any of the following integers: 2, 3, 4, 5, 6, and each of the above-mentioned specific integers can be used as other integers. The endpoint of a numerical range; b can be any of the following integers: 1, 2, 3, 4, 5, 6. Each of the above-mentioned specific integers can be used as the endpoint of other numerical ranges.

In this specification, the liquid chromatography method takes 30% to 70% by volume of methanol aqueous solution as the mobile phase, and combines the gradient extraction method and the iso-intensity extraction method for 90 minutes to complete. Preferably, in the first 60 minutes of the liquid chromatography method, 30 volume percent methanol aqueous solution is used as the mobile phase to gradually increase to the final 70 volume percent methanol aqueous solution as the mobile phase for gradient extraction, and then the next 30 minutes. Perform iso-strength extraction with 70% by volume methanol aqueous solution in minutes.

In this manual, the "low temperature environment" refers to an environment below room temperature, and it can also be an environment below zero. For example, the low temperature environment may be an environment of -20°C to 20°C, or may refer to an environment of 0°C to 10°C, -20°C to 0°C, -20°C to -5°C , Or -20°C to -15°C, but not limited to this.

In this specification, the "longer storage time" means that the melamine formaldehyde resin composition can be stored in a specific environment (such as a low temperature environment) for a longer period of time compared to commercially available products, and during this period of storage, the melamine The formaldehyde resin composition maintains a liquid state without generating crystals. Specifically, the "longer storage time" may mean that the storage time is greater than 1 day, preferably greater than 4 days, more preferably greater than 1 week, or even more than 2 weeks.

In order to achieve the foregoing objective, the present invention also provides a melamine formaldehyde resin product, which may include a melamine formaldehyde resin composition cured from the melamine formaldehyde resin composition of the aforementioned first aspect or second aspect. According to this creation, the melamine-formaldehyde resin composition of the aforementioned first aspect or the second aspect has excellent frost resistance and an appropriate low-temperature storage period, so it can help improve the operability and processability of the melamine-formaldehyde resin, so that it can be Suitable for making products in various application fields.

According to this creation, the melamine formaldehyde resin composition can be used as, for example, ink, wood paint, car paint, water-based paint, etc., but it is not limited to this. The melamine formaldehyde resin products can be wood processed products, paper processed products, fiber processed products, ink processed products, metal processed products (such as: car paint, color steel or coil, pre-coated metal plate (pre-coated metal )).

Hereinafter, several examples are listed to illustrate the implementation of the melamine formaldehyde resin composition, and several comparative examples are provided as controls. Those skilled in the art can easily understand the advantages and advantages of this creation from the content of the following examples and comparative examples. Effect. It should be understood that the embodiments listed in this specification are only used to exemplify the implementation of this creation, and are not used to limit the scope of this creation. Those skilled in the art can use their general knowledge to not deviate from the spirit of this creation. Make various modifications and changes to implement or apply the content of this creation.

"Melamine formaldehyde resin composition"

Example 1 to 7 ( S1 to S7 )

As shown in Figure 1, the melamine-formaldehyde resin compositions of Examples 1 to 7 were prepared by the method described below.

First, weigh 238 grams of paraform, add 171 grams of methanol and stir to form a mixed solution, then add sodium hydroxide to the mixed solution and adjust its pH to 10.5±0.5, and the mixed solution The temperature is raised to 50°C to completely dissolve the paraformaldehyde, and the mixed solution appears transparent at this time.

Next, add 106 grams of melamine to the above mixed solution, and again add sodium hydroxide to adjust its pH to 10.5±0.5, then add 94 grams of methanol, and then heat the mixed solution to 70°C and Keep it for 90 minutes.

After that, 65 g of methanol was added to the mixed solution again, and the etherification reaction was carried out according to the time shown in Table 1 below. When the etherification reaction is completed, the mixed solution is subjected to atmospheric distillation at 760 Torr and 98°C, and then under reduced pressure distillation at 80 Torr and 105°C.

Then, 270 grams of methanol was added to the mixed solution, hydrochloric acid was added to adjust the pH to 4.0±0.5 and maintained for 20 minutes, and then an appropriate amount of sodium hydroxide was added to adjust the pH to 9.5±0.5.

After that, the mixed solution was again subjected to atmospheric distillation at 760 Torr and 98°C, and then under reduced pressure distillation at 80 Torr and 105°C. After 60 minutes, the solid residue was filtered to prepare The melamine-formaldehyde resin compositions of Examples 1 to 7 were obtained.

Comparative example 1 to 3 ( C1 to C3 )

As shown in Figure 2, the melamine-formaldehyde resin compositions of Comparative Examples 1 to 3 were prepared by the method described below.

First, weigh 367.2 grams of hexamethylol melamine (HMM for short), add 413.3 grams of methanol, and stir to dissolve the HMM to obtain a mixed solution.

After that, the etherification reaction was carried out according to the time shown in Table 1 below. After the etherification reaction is completed, the mixed solution is subjected to atmospheric distillation at 760 Torr and 98°C, and then under reduced pressure distillation at 80 Torr and 115°C.

Then, 413.3 grams of methanol was added to the mixed solution, and hydrochloric acid was added to adjust its pH to 3.0±0.5, and then the temperature was raised to 69±1°C and maintained for 20 minutes. Then add sodium hydroxide to adjust the pH to 9.5±0.5.

After that, the mixed solution was again subjected to atmospheric distillation at 760 Torr and 98°C, and then under reduced pressure distillation at 80 Torr and 140°C. After 60 minutes, the solid residue was filtered to prepare The melamine-formaldehyde resin compositions of Comparative Examples 1 to 3 were obtained.

Test example 1 : High Performance Liquid Chromatography Mass Spectrometry ( HPLC-MS )analyze

In this test example, the melamine-formaldehyde resin composition of the foregoing Examples 1 to 7 and Comparative Examples 1 to 3 is used as the sample to be tested, and a High Performance Liquid Chromatography (HPLC) tandem mass spectrometer (Mass Spectroscopy, MS ) And perform measurement and analysis under the following conditions to obtain the relative proportions of the component structures and contents of the melamine-formaldehyde resin compositions of Examples 1 to 7 and Comparative Examples 1 to 3, respectively.

HPLC analysis parameters: 1. Brand: SHIMADZU, 2. System controller: SCL-20A, 3. Auto-injector: SIL-20A, 4. Pump: LC-20AT, 5. Detector: ultraviolet (UV)/visible light (Vis) SPD-20A, 6. Detection wavelength: 235 nanometers (nm), 7. Column: Inertsil ODS-2 (inner diameter 4.6 mm, length 250 mm, grain size 5 microns) 8. Mobile phase: (1) 0 to 60 minutes: use methanol: water (volume percentage) = 30: 70 solvent to gradually increase the concentration to methanol: water (volume percentage) = 70: 30 solvent, perform gradient extraction, and (2) 60 to 90 minutes: use methanol: water (volume percentage) = 70:30 solvent for equal intensity extraction, 9. Mobile phase flow rate: 1 milliliter (mL)/minute (min).

Analysis parameters of MS: 1. Instrument brand and model: SHIMADZU LCMS-8045, 2. Free source: Electrospray Ionization (ESI), 3. Nebulizing Gas Flow: 3 liters (L)/min, 4. Heating Gas Flow: 10 L/min, 5. Atomization temperature (Interface Temperature): 300°C, 6. DL Temperature: 250°C, 7. Dry gas temperature (Heat Block Temperature): 400°C, 8. Drying Gas Flow: 10 L/min, 9. Quality detector: Three sets of quadrupoles (Triple-Quadrupole, QqQ).

Please refer to Figures 3 to 12, which sequentially show the HPLC spectra of the melamine-formaldehyde resin compositions of Examples 1 to 7 (S1 to S7) and Comparative Examples 1 to 3 (C1 to C3) measured according to the above method , The area ratio of each chromatographic peak in each HPLC spectrum is shown in Table 1 below.

Here, the area of each chromatographic peak in the HPLC spectrum is interpreted by a computer. If the width of the x-axis in the HPLC spectrum is less than 5 seconds and the signal with UV intensity less than 200 per minute is judged as noise.

成分a (如式(VI))； 成分b (如式(VII))； 成分c (如式(IX))；      

成分d (如式(X))； 成分e (如式(II))； 成分f (如式(III))；      

成分g (如式(VIII))； 成分h (如式(IV))； 成分i (如式(V))。 In addition, the mass-to-charge ratios of the fractions collected under different extraction times using mass spectrometer analysis are also listed in Table 1 below, and the components corresponding to each fraction are separately shown in FIGS. 3-12. The melamine formaldehyde resin composition includes at least the following components:

Component a (as in formula (VI)); Component b (as in formula (VII)); Component c (as in formula (IX));

Component d (as in formula (X)); Ingredient e (as in formula (II)); Component f (as in formula (III));

Ingredient g (such as formula (VIII)); Component h (as in formula (IV)); Ingredient i (as in formula (V)).

Test example 2 ：Freezing resistance

In this test example, the melamine-formaldehyde resin composition of the foregoing Examples 1 to 7 and Comparative Examples 1 to 3 is used as the sample to be tested, and 10 milliliters (mL) of each sample to be tested is sampled and placed in a 20-ml sample bottle. Let each sample bottle stand at room temperature for about 1 hour to ensure that there are no bubbles in the sample bottle.

Next, store each sample bottle in a refrigerator at -15°C (low temperature environment), and check the liquid level of the sample to be tested or the wall surface of the sample bottle at the same time the next day (the second day) for crystallization. If the sample to be tested is stored in a low temperature environment and crystallization is observed on the second day, it means that the low temperature storage period of the sample is less than 1 day, which is expressed as "<1 day". If no crystallization is observed on the second day, it means that the sample to be tested has at least one day's frost resistance. After recording, put it back into the refrigerator at -15°C and wait for one day before continuing to observe. If no crystallization is observed on the second day but crystallization is observed on the third day, it means that the low-temperature storage period of the sample to be tested is only 1 day but less than 2 days, so the low-temperature storage period is expressed as "1 day"; on the other hand, If no crystallization is observed on the 3rd day, it means that the sample to be tested has at least 2 days of frost resistance. After recording, put it back into the refrigerator at -15°C and continue to observe on the 4th day. Continue to observe for several days every day according to the aforementioned method. If no crystallization is observed on the 15th day, it means that the sample to be tested has at least 14 days of frost resistance. After the low-temperature storage period is recorded as "≧14 days", it shows The sample to be tested has at least 2 weeks of frost resistance. The low temperature storage period of each sample is listed in Table 1 below. Table 1: The etherification time of the melamine formaldehyde resin composition of Examples 1 to 7 (S1 to S7) and Comparative Examples 1 to 3 (C1 to C3), the chromatographic peak area ratio of each component and the low temperature storage period. S1 S2 S3 S4 S5 S6 S7 C1 C2 C3 Etherification time (minutes) 43 55 42 50 52 45 48 56 50 46 Element m/z Chromatographic peak area ratio (%) a 303 1.34 1.32 1.38 1.43 1.39 1.19 2.11 1.20 1.11 1.02 b 333 0.51 0.65 0.56 0.59 0.59 0.92 2.46 0.57 0.36 0.50 c 347 9.70 10.39 10.27 10.84 10.67 10.42 13.17 10.03 10.50 10.30 d 377 2.00 3.12 2.07 2.60 2.33 4.89 8.67 1.86 1.59 2.78 e 393 1.04 1.09 1.19 0.84 0.89 1.73 3.07 0.28 0.26 0.22 f 407 0.23 0.39 0.25 0.24 0.23 0.91 1.98 0.05 0.04 0.06 g 391 26.31 29.66 27.45 30.71 30.29 28.80 20.32 34.82 33.19 39.02 h 421 5.37 6.32 5.76 4.37 4.26 7.17 5.34 1.02 1.20 1.16 i 451 0.49 0.62 0.55 0.37 0.37 0.75 0.68 0.07 0.07 0.05 a+b - 1.85 1.97 1.94 2.02 1.98 2.11 4.57 1.77 1.47 1.52 e+f+h+i - 7.13 8.42 7.75 5.82 5.75 10.56 11.07 1.42 1.57 1.49 Low temperature storage period (days) ≧14 ≧14 ≧14 8 5 ≧14 ≧14 <1 1 <1

"Experimental Results Discussion"

It can be seen from Table 1 that, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the chromatographic peaks with a mass-to-charge ratio of 393 to 692 (for example, in the melamine formaldehyde resin composition of Examples 1 to 7) The total area of the chromatographic peaks of components e, f, h and i) is 2% to 20%; on the contrary, the melamine-formaldehyde resin composition of Comparative Examples 1 to 3 does not fall within the aforementioned range, that is to say, The total area of all the chromatographic peaks in the melamine-formaldehyde resin composition is a reference. The total area of the chromatographic peaks in the melamine-formaldehyde resin composition of Comparative Examples 1 to 3 with a mass-to-charge ratio of 393 to 692 is less than 2%. Therefore, comparing the low-temperature storage period of the melamine-formaldehyde resin composition of Examples 1 to 7 and Comparative Examples 1 to 3, the melamine-formaldehyde resin composition of Examples 1 to 7 has a low-temperature storage period of at least 5 days or more. It has a low-temperature storage period of more than 14 days, but the melamine-formaldehyde resin compositions of Comparative Examples 1 to 3 only have a low-temperature storage period of one day or even less than one day. Therefore, the experimental results show that controlling the area ratio of the chromatographic peaks with a mass-to-charge ratio of 393 to 692 can help increase the frost resistance of the melamine-formaldehyde resin composition and obtain a longer low-temperature storage period. In addition, those with ordinary knowledge in this technical field can also understand that controlling the area ratio of the chromatographic peaks of other melamine oligomers similar to components e, f, h and i will also help improve the melamine formaldehyde resin composition. The anti-freezing effect of the product, extending its storage time in low temperature environment.

On the other hand, analyze the experimental results in Table 1 above. Based on the total area of all chromatographic peaks in the melamine-formaldehyde resin composition, the ingredients in the melamine-formaldehyde resin composition of Examples 1 to 7 are g (2, 4, The area of the chromatographic peak of 6-tris[bis(methoxymethyl)amino]-1,3,5-triazine) is less than 33%; and the component g in the melamine-formaldehyde resin composition of Comparative Examples 1 to 3 The area of the chromatographic peak is higher than 33%. To compare the low-temperature storage period of the melamine-formaldehyde resin composition of Examples 1 to 7 and Comparative Examples 1 to 3, the melamine-formaldehyde resin composition of Examples 1 to 7 has a low-temperature storage period of at least 5 days or more. Examples 1 to 3 And 6 to 7 even have a low temperature storage period of more than 14 days, but the melamine-formaldehyde resin compositions of Comparative Examples 1 to 3 only have a low temperature storage period of one day or even less than one day. Experimental results show that by controlling the area ratio of the chromatographic peaks of component g, it is helpful to inhibit or reduce the formation of crystals, thereby enhancing the antifreeze effect of the melamine formaldehyde resin composition and prolonging its storage time in a low temperature environment.

In addition, the components of the melamine-formaldehyde resin composition of Examples 1 to 7 were further analyzed, and chromatographic peaks with the mass-to-charge ratio of 300 to 310 (for example, the chromatographic peak of component a) and the mass-to-charge ratio of 330 to 310 were observed. The total area of the chromatographic peak of 340 (such as the chromatographic peak of component b) is controlled to be higher than 1.80%, which can also increase the frost resistance of the melamine formaldehyde resin composition, so that each has a low temperature storage period of at least 5 days.

To sum up, this creation adjusts the area of the chromatographic peaks of specific components in the melamine-formaldehyde resin composition, for example, adjusts the area ratio of the chromatographic peaks of melamine oligomers (components e, f, h, and i) Or adjust the area ratio of the chromatographic peak of 2,4,6-tris[bis(methoxymethyl)amino]-1,3,5-triazine (component g), which can effectively inhibit melamine formaldehyde The resin composition produces crystals and increases the frost resistance of the melamine formaldehyde resin composition, thereby improving the low-temperature storage period and the application range of the melamine formaldehyde resin composition.

without

Fig. 1 is a schematic view of the process of manufacturing the melamine-formaldehyde resin composition of Examples 1-7. Fig. 2 is a schematic view of the process of manufacturing the melamine-formaldehyde resin composition of Comparative Examples 1 to 3. 3 to 9 are HPLC diagrams of the melamine-formaldehyde resin composition of Examples 1 to 7 in sequence. 10 to 12 are HPLC diagrams of the melamine-formaldehyde resin compositions of Comparative Examples 1 to 3 in sequence.

Claims (12)

A melamine formaldehyde resin composition comprising 2,4,6-tris[bis(methoxymethyl)amino]-1,3,5-triazine represented by the following formula (VIII):

Wherein the melamine formaldehyde resin composition is analyzed by liquid chromatography combined with mass spectrometry, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the 2,4,6-tris[bis(methoxy) The area of the chromatographic peak of methyl)amino]-1,3,5-triazine is 15% to 31%. The melamine-formaldehyde resin composition according to claim 1, wherein the 2,4,6-tris[bis(methoxymethyl)amine is based on the total area of all chromatographic peaks in the melamine-formaldehyde resin composition The area of the chromatographic peak of the radical]-1,3,5-triazine is 20% to 31%. The melamine-formaldehyde resin composition according to claim 1, wherein the 2,4,6-tris[bis(methoxymethyl)amine is based on the total area of all chromatographic peaks in the melamine-formaldehyde resin composition The area of the chromatographic peak of the radical]-1,3,5-triazine is 20% to 28%. The melamine formaldehyde resin composition according to any one of claims 1 to 3, wherein the melamine formaldehyde resin composition further comprises at least one melamine oligomer, wherein the mass-to-charge ratio of the at least one melamine oligomer is from 393 to 692. Based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the total area of the chromatographic peaks with a mass-to-charge ratio of 393 to 692 is 2% to 20%. The melamine formaldehyde resin composition according to claim 4, wherein the at least one melamine oligomer has a structure represented by the following formula (I):

Wherein, a is an integer from 2 to 6, b is an integer from 1 to 6, and R ₁ and R ₂ are each independently a hydroxyl group or a methoxy group. The melamine formaldehyde resin composition according to claim 5, wherein the mass-to-charge ratio of the at least one melamine oligomer is 393 to 452, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the mass The sum of the areas of the chromatographic peaks with charge ratios of 393 to 452 is 5% to 15%. The melamine formaldehyde resin composition according to claim 5, wherein the mass-to-charge ratio of the at least one melamine oligomer is 393 to 452, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the mass The sum of the areas of the chromatographic peaks with charge ratios of 393 to 452 is 7% to 12%. The melamine formaldehyde resin composition according to claim 5, wherein the mass-to-charge ratio of the at least one melamine oligomer is 393 to 452, based on the total area of all chromatographic peaks in the melamine formaldehyde resin composition, the mass The sum of the areas of the chromatographic peaks with charge ratios of 393 to 452 is 5% to 8%. The melamine-formaldehyde resin composition according to claim 6, wherein the at least one melamine oligomer has a structure represented by the following formula (II) to formula (V):

The melamine-formaldehyde resin composition according to any one of claims 1 to 3, wherein the melamine-formaldehyde resin composition further comprises a component represented by the following formula (VI):

Wherein the mass-to-charge ratio of the component represented by the formula (VI) is 300 to 310, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the area of the chromatographic peak with the mass-to-charge ratio of 300 to 310 The sum is 1.15% to 2.5%. The melamine formaldehyde resin composition according to claim 10, wherein the melamine formaldehyde resin composition further comprises a component represented by the following formula (VII):

Wherein the mass-to-charge ratio of the component represented by the formula (VII) is 330 to 340, based on the total area of all the chromatographic peaks in the melamine formaldehyde resin composition, the area of the chromatographic peak with the mass-to-charge ratio of 300 to 310 The sum of the areas of the chromatographic peaks with a mass-to-charge ratio of 330 to 340 is 1.8% to 5.0%. A melamine-formaldehyde resin product, which is formed by curing the melamine-formaldehyde resin composition according to any one of claims 1 to 11.

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