In September 2021, we received an inquiry from Mr. Abdullah in Saudi Arabia regarding a continuous foaming machine. The client was planning to establish a PU foam factory to produce products for the local and Yemeni markets. He had some basic knowledge about machine usage and selection.

The client had no prior experience in foam production before, so he was particularly concerned about after-sales support and technical assistance.

We began by analyzing the client's target market (specific industry) and understanding the local product requirements (such as foam density, hardness, etc.) to confirm the client's production needs.

Through video conferences, we guided the client through our PU foam production process, providing the client with a concrete understanding of foam production and highlighting the convenience and efficiency advantages of our machines compared to those of other manufacturers.

Drawing upon our more than 20 years of experience in foam foaming, we shared insights with the client about using the machine and common challenges in the foam foaming process, addressing any technical concerns the client may have had.

We also provided the client with factory layout plans to expedite the setup of the entire foam production line while maximizing production efficiency.

Due to the client's high level of trust in our professional service, he ultimately chose us as his supplier for foam machinery and later made repeat purchases for a rebonded foam production line and foam cutting machines.

The compressive resistance of a foam is related to many factors such as the structure of various chain segments composing the foam, the chemical bonds between molecules, the crystallinity of polymers, the degree of phase separation, the structure of isocyanates, and the proportion of isocyanates used.

1. Slow rebound foam is formed by the reaction of high molecular weight polyols and low molecular weight polyols with isocyanates. The soft segments formed by high molecular weight polyols have large volumes, low crosslink densities, and high activity. They are easy to compress and quickly recover after pressure is removed. The hard segments formed by low molecular weight polyols have small volumes, high crosslink densities, and low activity. They are difficult to compress and also difficult to recover after external forces are removed. This characteristic gives foams their slow rebound feature and is the basis for manufacturing slow rebound foams.

Because the properties of the soft and hard segments in slow rebound foams are different, there is a certain degree of phase separation between them. If there is no phase separation between the segments, the foam body is a tightly bound whole on a macro scale, leading to the phenomenon of "move one hair and the whole body moves," meaning it shrinks as a whole when compressed and expands when pressure is released. However, the microstructure of the foam determines that this situation cannot be achieved completely. Especially in slow rebound foams, various chain segments have different molecular structures, uneven molecular weight distributions, and unavoidable phase separation. Slight phase separation causes some hard segments, due to their low activity, to have difficulty recovering during the recovery process after external forces are removed. These "escapees" more or less restrain the recovery of soft segments, ultimately leading to shrinking.

2. The crystallinity of hard segments, which is stronger than that of soft segments, is also a reason for poor recovery. Materials have similar compatibilities, which also apply in slow rebound foams. Because the hard segments have closer cross-linking points and higher crosslink densities, the small molecules formed are more likely to aggregate together. Due to the presence of hydrogen bonds, these aggregated hydrogen-containing substances enhance the crystallinity of the material, leading to greater cohesive forces. After compression, external forces change the aggregation state of the chain segments, making it easier for polar groups to fuse together. When the external force is released, the new aggregation state, due to strong cohesive forces, is difficult to return to the pre-stressed state, resulting in shrinkage of slow rebound foams.

3. The structure of isocyanates is also a factor affecting the compression resistance of slow rebound foams. TDI is usually used to produce slow rebound foams. Because the two NCO groups in the TDI molecule are at the 2,4- and 2,6- positions, they have a certain angle between them, making them prone to deformation under stress. Especially under hot pressing conditions, significant deformation and heat loss occur, particularly evident in bra cup foams, making recovery from these deformations difficult.

4. The low NCO index of isocyanates used in the preparation of slow rebound foams is also a reason for poor recovery. The NCO index of ordinary foams is usually above 100, while in slow rebound foams , the NCO index is generally between 85-95. This means that 5-15% of the hydroxyl groups do not participate in the reaction. Therefore, although the surface of the foam appears to be a single entity, internally there is a considerable portion of chain segments that are independent of each other.

Solutions for Improving Compression Resistance of Slow Rebound Foams:

1.Use high EO polyether (so-called blowing agent polyether) to replace some slow rebound polyether.

A. High EO polyether has a low hydroxyl value and a large molecular weight. After reacting with isocyanates, the segments formed have molecular weights greater than or close to those formed when ordinary polyether reacts with isocyanates, reducing the degree of phase separation and crystallinity.

B. High EO content polyether has soft and smooth segments, which can provide good slow rebound effects. Additionally, the addition of high EO polyether can effectively improve the low-temperature resistance of slow rebound foams.

2.Add a small amount of polyether-modified polyester to increase the material's cohesive force.

The polyester segments, due to the presence of ester groups, have high internal cohesive forces and good tensile and compressive properties, significantly improving the compressive resistance of slow rebound foams.

3.Use a small amount of high-functionality and high molecular weight polyether as a crosslinking agent, and replace some ordinary polyether with high-activity polyether for slow rebound.

This disrupts the distribution of chain segments, reduces the degree of phase separation, and increases the reaction degree, reducing crystallinity.

4.Use MDI or add MDI to TDI.

MDI has a different structure from TDI and produces foams with better compression resistance and less heat loss. If using MDI, it is best to use modified MDI (with high branching and easy closure of cells); liquid MDI can also be used, as it is intramolecular cyclization and more resistant to compression. Slow rebound foams made with all MDI have much better compression resistance than pure TDI, and many manufacturers are already using this.

Foam scorching is a common phenomenon encountered in actual foam production. Below are the reasons behind this issue along with potential solutions:

(1) Issues with the quality of polyether polyols: During production and transportation, the product's water content exceeds the standard, there is an excess of peroxides and low-boiling-point impurities, the concentration of metal ions is too high, and there is improper selection and concentration of antioxidants.

(2) Formulation: In low-density formulations, the TDI index is too high, the proportion of water to physical blowing agents in the foaming agent is improper, the amount of physical blowing agent is insufficient, and there is excessive water content.

(3) Climate impact: In summer, high temperatures lead to slow heat dissipation, high material temperatures, high air humidity, and the temperature at the reaction center exceeds the antioxidant temperature.

(4) Improper storage: When the TDI index increases, the accumulated heat energy during post-maturation causes an increase in internal temperature, leading to scorching.

Understanding the principles behind foam reactions is crucial. To master foaming, we must strive to establish a foam reaction model in our minds using the following four reaction equations. Through familiarity with the variations within the model, we cultivate sensitivity that allows us to comprehend the entire foam reaction process. This approach helps structure our knowledge base and professional skills in polyurethane foam. Whether actively studying foam reaction principles or passively exploring them during the foaming process, it serves as a vital means for us to deepen our understanding of formulations and enhance our skills.

Reaction 1

TDI + Polyether → Urethane

Reaction 2

TDI + Urethane → Isocyanurate

Reaction 3

TDI + Water → Urea + Carbon Dioxide

Reaction 4

TDI + Urea → Biuret (Polyurea)

01: Reactions 1 and 2 are chain-growth reactions, forming the main chain of the foam. Before the foam reaches two-thirds of its maximum height, the main chain rapidly elongates, with chain-growth reactions predominating inside the foam. At this stage, due to relatively low internal temperatures, reactions 3 and 4 are not prominent.

02: Reactions 3 and 4 are cross-linking reactions, forming the branches of the foam. Once the foam reaches two-thirds of its maximum height, the internal temperature rises, and reactions 3 and 4 intensify rapidly. During this stage, reactions 1 to 4 are vigorous, marking a critical period for the formation of foam properties. Reactions 3 and 4 provide stability and support to the foam system. Reaction 1 contributes to foam elasticity, while reactions 3 and 4 contribute to foam tensile strength and hardness.

03: Gas-producing reactions are termed foaming reactions. The generation of carbon dioxide is a foaming reaction and the primary exothermic reaction in polyurethane foam. In reaction systems containing methane, the vaporization of methane constitutes a foaming reaction and an endothermic process.

04: Reactions leading to the formation of foam constituents are known as gelation reactions, encompassing all reactions except for gas-producing reactions. This includes the formation of urethane, urea, isocyanurate, and biuret (polyurea) from reactions 1 to 4.

Have you ever wondered how polyurethane plastic foam is formed? In the previous article, we revealed the basic reactions behind it: isocyanates, polyether (or polyester) polyols, and water, all work together to create this magical substance. So, does this mean that in actual production, we only need these three raw materials? The answer is far from it. In our actual production process, in order to more precisely control the reaction rate and produce products with excellent performance, we often need to harness the power of various additives. These additives not only have wide-ranging applications but also can play a huge role in making our production process more efficient and stable.

Surfactants / Silicone Oil

Surfactants, also known as silicone oil, are also called foam stabilizers. In the production process of polyurethane foam, its role is crucial. The basic duty of silicone oil is to reduce the surface tension of the foaming system, thus improving the miscibility between components, adjusting the size of bubbles, controlling the bubble structure, and enhancing foam stability. Furthermore, it also bears the responsibility of preventing foam collapse. Therefore, it can be said that silicone oil plays an indispensable role in the production of polyurethane foam.

Catalysts

Catalysts play a crucial role in the synthesis process of polyurethane, mainly by accelerating the reaction between isocyanates, water, and polyols. This reaction is a typical polymerization reaction. Without the presence of catalysts, this reaction may proceed very slowly or even not at all. Currently, catalysts on the market are mainly divided into two types: amine catalysts and organic metal catalysts. Amine catalysts are compounds based on nitrogen atoms, which can effectively promote the polymerization reaction of polyurethane. Organic metal catalysts, on the other hand, are compounds that particularly affect the reaction between polyols and isocyanates in the formation of polyurethane, usually organotin compounds. The characteristic of these catalysts lies in their ability to precisely control the reaction process, resulting in a more uniform and stable final product.

Blowing Agents

Blowing agents are substances that generate gas during the polyurethane reaction and help form foam. Depending on the way gas is generated, blowing agents are usually divided into chemical blowing agents and physical blowing agents. Chemical blowing agents refer to substances that undergo chemical changes during the reaction, generate gas, and promote foam formation. Many common substances in our daily lives are actually chemical blowing agents, such as water. Physical blowing agents, on the other hand, are substances that generate gas through physical means. For example, dichloromethane (MC) is a common physical blowing agent.

Other Additives

Relying solely on basic raw materials is far from enough to make products have outstanding performance. In order to meet various needs, other additives are cleverly incorporated into the production process, and their roles should not be underestimated. For example, flame retardants can add flame resistance to products, crosslinking agents can enhance their stability, colorants and fillers can give products a more colorful appearance and texture, and various other additives with different functions are also playing their roles. It is these carefully selected additives that comprehensively improve the performance of the products and bring users a better user experience.