{"id":59844,"date":"2025-04-05T18:18:25","date_gmt":"2025-04-05T10:18:25","guid":{"rendered":"http:\/\/www.newtopchem.com\/archives\/59844"},"modified":"2025-04-05T18:18:25","modified_gmt":"2025-04-05T10:18:25","slug":"the-role-of-polyurethane-catalyst-dmap-in-reducing-voc-emissions-for-green-chemistry","status":"publish","type":"post","link":"http:\/\/www.newtopchem.com\/archives\/59844","title":{"rendered":"The Role of Polyurethane Catalyst DMAP in Reducing VOC Emissions for Green Chemistry","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"The Role of Polyurethane Catalyst DMAP in Reducing VOC Emissions for Green Chemistry<\/h2>\n
Contents<\/strong><\/p>\n\n- Introduction<\/li>\n
- Polyurethane Chemistry and VOC Emissions\n
\n- Polyurethane Synthesis<\/li>\n
- Sources of VOC Emissions in Polyurethane Production<\/li>\n
- Environmental and Health Concerns<\/li>\n<\/ul>\n<\/li>\n
- DMAP: Structure, Properties, and Catalytic Mechanism\n
\n- Chemical Structure and Physical Properties<\/li>\n
- Catalytic Mechanism in Polyurethane Synthesis<\/li>\n
- Advantages of DMAP as a Catalyst<\/li>\n<\/ul>\n<\/li>\n
- DMAP in Reducing VOC Emissions\n
\n- Enhancing Reaction Rate and Conversion<\/li>\n
- Promoting Isocyanate Consumption<\/li>\n
- Influence on Polyurethane Microstructure<\/li>\n<\/ul>\n<\/li>\n
- Applications of DMAP in Various Polyurethane Systems\n
\n- Rigid Polyurethane Foams<\/li>\n
- Flexible Polyurethane Foams<\/li>\n
- Coatings, Adhesives, Sealants, and Elastomers (CASE)<\/li>\n<\/ul>\n<\/li>\n
- Green Chemistry Aspects of DMAP Utilization\n
\n- Atom Economy and Waste Reduction<\/li>\n
- Energy Efficiency and Process Optimization<\/li>\n
- Safer Solvents and Reduced Toxicity<\/li>\n<\/ul>\n<\/li>\n
- Challenges and Future Directions\n
\n- Cost Considerations<\/li>\n
- Potential Toxicity and Safety Concerns<\/li>\n
- Research and Development Opportunities<\/li>\n<\/ul>\n<\/li>\n
- Conclusion<\/li>\n
- References<\/li>\n<\/ul>\n
\nIntroduction<\/strong><\/p>\nPolyurethane (PU) materials are ubiquitous in modern life, finding applications in diverse sectors such as construction, transportation, furniture, and packaging. Their versatility stems from the ability to tailor their properties \u2013 hardness, flexibility, density, and thermal resistance \u2013 by varying the isocyanate and polyol components, as well as through the use of additives and catalysts. However, the production of polyurethane often involves the release of volatile organic compounds (VOCs), which pose significant environmental and health hazards. The increasing global focus on sustainable development and green chemistry has spurred research into alternative catalysts that can minimize VOC emissions while maintaining or improving the performance of polyurethane products.<\/p>\n
4-Dimethylaminopyridine (DMAP) has emerged as a promising catalyst in polyurethane chemistry due to its high catalytic activity, ability to promote specific reactions, and potential for reducing VOC emissions. This article delves into the role of DMAP in reducing VOC emissions for green chemistry, exploring its structure, properties, catalytic mechanism, applications in various polyurethane systems, and its contribution to sustainable polyurethane production.<\/p>\n
Polyurethane Chemistry and VOC Emissions<\/strong><\/p>\n\n- Polyurethane Synthesis<\/strong><\/li>\n<\/ul>\n
Polyurethanes are typically synthesized through the step-growth polymerization of a polyol (an alcohol containing multiple hydroxyl groups) and an isocyanate (a compound containing one or more isocyanate groups -N=C=O). The fundamental reaction involves the nucleophilic attack of the hydroxyl group of the polyol on the electrophilic carbon of the isocyanate group, forming a urethane linkage (-NH-COO-).<\/p>\n
R-N=C=O + R'-OH \u2192 R-NH-COO-R'\n(Isocyanate) (Polyol) (Urethane)<\/code><\/pre>\nThis reaction can be represented as shown in the equation above. The isocyanate component is often diphenylmethane diisocyanate (MDI) or toluene diisocyanate (TDI), while the polyol component can be a polyester polyol, polyether polyol, or a combination thereof. Various additives, such as surfactants, blowing agents, and flame retardants, are often incorporated to modify the properties of the final product.<\/p>\n
\n- Sources of VOC Emissions in Polyurethane Production<\/strong><\/li>\n<\/ul>\n
VOC emissions from polyurethane production arise from several sources:<\/p>\n
* **Unreacted Isocyanate:** Isocyanates, particularly TDI, are known to have high vapor pressures and can be emitted into the atmosphere if not completely reacted. Residual isocyanate can also react with moisture in the air, forming polyureas and releasing carbon dioxide.\n* **Blowing Agents:** Chemical blowing agents (CBAs), such as water, which react with isocyanate to produce carbon dioxide, and physical blowing agents (PBAs), such as pentane or methylene chloride, are used to create cellular structures in foams. PBAs can be significant sources of VOC emissions, especially if not efficiently captured or destroyed.\n* **Solvents:** Solvents are often used to dissolve or disperse components, clean equipment, or adjust the viscosity of the reaction mixture. Many common solvents, such as toluene, xylene, and methyl ethyl ketone (MEK), are VOCs.\n* **Additives:** Some additives, such as certain flame retardants and plasticizers, can also contribute to VOC emissions.\n* **Catalysts:** Tertiary amine catalysts, traditionally used in polyurethane production, can themselves be VOCs or can promote side reactions that generate VOCs.<\/code><\/pre>\n\n- Environmental and Health Concerns<\/strong><\/li>\n<\/ul>\n
VOC emissions from polyurethane production pose several environmental and health concerns:<\/p>\n
* **Air Pollution:** VOCs contribute to the formation of ground-level ozone and smog, which can cause respiratory problems and damage vegetation.\n* **Greenhouse Gas Emissions:** Some VOCs are greenhouse gases, contributing to climate change.\n* **Health Hazards:** Exposure to VOCs can cause a range of health effects, including eye, nose, and throat irritation, headaches, nausea, dizziness, and in some cases, cancer.\n* **Isocyanate Exposure:** Isocyanates are potent respiratory sensitizers and can cause asthma and other respiratory problems. Even low levels of exposure can trigger reactions in sensitized individuals.<\/code><\/pre>\nDMAP: Structure, Properties, and Catalytic Mechanism<\/strong><\/p>\n\n- Chemical Structure and Physical Properties<\/strong><\/li>\n<\/ul>\n
DMAP (4-Dimethylaminopyridine) is an organic compound with the chemical formula (CH3)2NC5H4N. It is a derivative of pyridine with a dimethylamino group at the 4-position.<\/p>\n
\n\n\n| Property<\/th>\n | Value<\/th>\n<\/tr>\n<\/thead>\n |
\n\n| Molecular Formula<\/td>\n | C7H10N2<\/td>\n<\/tr>\n |
\n| Molecular Weight<\/td>\n | 122.17 g\/mol<\/td>\n<\/tr>\n |
\n| Appearance<\/td>\n | White to off-white crystalline solid<\/td>\n<\/tr>\n |
\n| Melting Point<\/td>\n | 112-115 \u00b0C<\/td>\n<\/tr>\n |
\n| Boiling Point<\/td>\n | 259-260 \u00b0C<\/td>\n<\/tr>\n |
\n| Density<\/td>\n | 1.03 g\/cm\u00b3<\/td>\n<\/tr>\n |
\n| Solubility<\/td>\n | Soluble in water, alcohols, and other organic solvents<\/td>\n<\/tr>\n |
\n| pKa<\/td>\n | 9.6 (conjugate acid)<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n DMAP is a strong nucleophilic catalyst due to the electron-donating dimethylamino group, which enhances the electron density on the pyridine nitrogen atom. Its high melting point and boiling point contribute to its lower volatility compared to traditional tertiary amine catalysts, making it potentially less prone to VOC emissions.<\/p>\n \n- Catalytic Mechanism in Polyurethane Synthesis<\/strong><\/li>\n<\/ul>\n
DMAP catalyzes the urethane reaction through a nucleophilic mechanism. The process can be summarized as follows:<\/p>\n 1. **Formation of an Acylpyridinium Intermediate:** DMAP initially reacts with the isocyanate to form a highly reactive acylpyridinium intermediate. The nitrogen atom of DMAP, being highly nucleophilic, attacks the electrophilic carbon of the isocyanate group.\n\n2. **Activation of the Alcohol:** The acylpyridinium intermediate then activates the hydroxyl group of the polyol, making it more nucleophilic and susceptible to attack by the isocyanate. This activation is achieved through hydrogen bonding or proton transfer.\n\n3. **Urethane Formation and Catalyst Regeneration:** The activated polyol attacks the carbonyl carbon of the acylpyridinium intermediate, forming the urethane linkage and regenerating the DMAP catalyst.<\/code><\/pre>\nThis catalytic mechanism is often described as a "nucleophilic catalysis" or "acyl transfer catalysis." The acylpyridinium intermediate is key to the reaction, facilitating the efficient transfer of the acyl group from the isocyanate to the alcohol.<\/p>\n \n- Advantages of DMAP as a Catalyst<\/strong><\/li>\n<\/ul>\n
DMAP offers several advantages as a catalyst in polyurethane synthesis:<\/p>\n * **High Catalytic Activity:** DMAP is significantly more active than traditional tertiary amine catalysts, such as triethylamine (TEA) or dimethylcyclohexylamine (DMCHA), in promoting the urethane reaction. This allows for lower catalyst loadings, which can reduce the overall cost of the formulation.\n* **Selectivity:** DMAP exhibits high selectivity for the urethane reaction, minimizing the formation of undesirable side products such as allophanates and biurets, which can negatively impact the properties of the polyurethane material.\n* **Lower Volatility:** DMAP has a lower vapor pressure compared to many traditional tertiary amine catalysts, potentially reducing VOC emissions during processing and application.\n* **Improved Mechanical Properties:** The use of DMAP can lead to improved mechanical properties of the polyurethane material, such as tensile strength, elongation at break, and tear resistance. This is often attributed to the more controlled and complete reaction achieved with DMAP.\n* **Reduced Odor:** DMAP has a less offensive odor compared to some tertiary amine catalysts, improving the working environment for polyurethane manufacturers.<\/code><\/pre>\nDMAP in Reducing VOC Emissions<\/strong><\/p>\n\n- Enhancing Reaction Rate and Conversion<\/strong><\/li>\n<\/ul>\n
DMAP’s high catalytic activity enables a faster reaction rate and higher conversion of isocyanate and polyol. This is crucial for reducing VOC emissions because it minimizes the amount of unreacted isocyanate remaining in the final product. Unreacted isocyanate can volatilize and contribute significantly to VOC emissions, as well as react with atmospheric moisture to form polyureas and release carbon dioxide. By accelerating the reaction and ensuring complete conversion, DMAP effectively reduces the source of isocyanate emissions.<\/p>\n \n- Promoting Isocyanate Consumption<\/strong><\/li>\n<\/ul>\n
The enhanced reaction rate promoted by DMAP leads to more efficient consumption of isocyanate. This is particularly important in formulations using high isocyanate indices (the ratio of isocyanate groups to hydroxyl groups), which are often employed to achieve specific performance characteristics. DMAP allows for the use of lower isocyanate indices while maintaining the desired properties, thereby reducing the overall amount of isocyanate required and consequently minimizing potential emissions.<\/p>\n \n- Influence on Polyurethane Microstructure<\/strong><\/li>\n<\/ul>\n
DMAP can influence the microstructure of the polyurethane material by affecting the rate of the urethane and urea reactions. The balance between these reactions determines the degree of phase separation between the hard segments (derived from isocyanate and chain extender) and the soft segments (derived from polyol). A well-defined microstructure with optimal phase separation can lead to improved mechanical properties and thermal stability, reducing the need for excessive amounts of additives that may contribute to VOC emissions. Furthermore, a more uniform and complete reaction can minimize the formation of low-molecular-weight oligomers that can volatilize and contribute to VOC emissions.<\/p>\n Applications of DMAP in Various Polyurethane Systems<\/strong><\/p>\n\n- Rigid Polyurethane Foams<\/strong><\/li>\n<\/ul>\n
Rigid polyurethane foams are widely used for insulation in buildings, appliances, and industrial applications. DMAP can be used to catalyze the reaction between isocyanates and polyols in rigid foam formulations, leading to:<\/p>\n * **Improved Foam Structure:** DMAP can promote a more uniform and fine-celled foam structure, which enhances insulation performance and mechanical strength.\n* **Reduced Blowing Agent Usage:** The improved reaction efficiency achieved with DMAP can reduce the need for blowing agents, particularly physical blowing agents that are major contributors to VOC emissions.\n* **Faster Demold Time:** DMAP's high catalytic activity can shorten the demold time, increasing production throughput and reducing energy consumption.\n* **Lower VOC Emissions:** By minimizing unreacted isocyanate and reducing the reliance on VOC-containing blowing agents, DMAP contributes to lower VOC emissions from rigid foam production.<\/code><\/pre>\n\n\n\n| Property<\/th>\n | Traditional Catalyst (Tertiary Amine)<\/th>\n | DMAP Catalyst<\/th>\n | Improvement<\/th>\n<\/tr>\n<\/thead>\n | \n\n| Cell Size (mm)<\/td>\n | 0.5 – 1.0<\/td>\n | 0.2 – 0.5<\/td>\n | Finer Cell Structure<\/td>\n<\/tr>\n | \n| Demold Time (min)<\/td>\n | 5 – 10<\/td>\n | 3 – 7<\/td>\n | Faster<\/td>\n<\/tr>\n | \n| Unreacted Isocyanate (%)<\/td>\n | 1 – 3<\/td>\n | 0.5 – 1.5<\/td>\n | Lower<\/td>\n<\/tr>\n | \n| VOC Emissions (ppm)<\/td>\n | 50 – 100<\/td>\n | 20 – 50<\/td>\n | Lower<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n\n- Flexible Polyurethane Foams<\/strong><\/li>\n<\/ul>\n
Flexible polyurethane foams are used in mattresses, furniture, automotive seating, and other cushioning applications. DMAP can be used to catalyze the reaction between isocyanates and polyols in flexible foam formulations, resulting in:<\/p>\n * **Enhanced Foam Resilience:** DMAP can improve the resilience and comfort of flexible foams by promoting a more controlled and uniform reaction.\n* **Reduced Amine Emissions:** DMAP can reduce the levels of amine emissions from the foam, improving air quality and reducing odor.\n* **Lower Catalyst Loading:** The high catalytic activity of DMAP allows for lower catalyst loadings compared to traditional tertiary amine catalysts, reducing the overall cost of the formulation and minimizing potential emissions.\n* **Improved Processing Window:** DMAP can widen the processing window, making the foam production process more robust and less sensitive to variations in raw materials and processing conditions.<\/code><\/pre>\n\n\n\n| Property<\/th>\n | Traditional Catalyst (Tertiary Amine)<\/th>\n | DMAP Catalyst<\/th>\n | Improvement<\/th>\n<\/tr>\n<\/thead>\n | \n\n| Tensile Strength (kPa)<\/td>\n | 100 – 150<\/td>\n | 120 – 180<\/td>\n | Higher<\/td>\n<\/tr>\n | \n| Elongation (%)<\/td>\n | 200 – 250<\/td>\n | 220 – 280<\/td>\n | Higher<\/td>\n<\/tr>\n | \n| Amine Emissions (ppm)<\/td>\n | 10 – 20<\/td>\n | 5 – 10<\/td>\n | Lower<\/td>\n<\/tr>\n | \n| Catalyst Loading (%)<\/td>\n | 0.5 – 1.0<\/td>\n | 0.2 – 0.5<\/td>\n | Lower<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n\n- Coatings, Adhesives, Sealants, and Elastomers (CASE)<\/strong><\/li>\n<\/ul>\n
In CASE applications, DMAP can be used to catalyze the reaction between isocyanates and polyols in various formulations, leading to:<\/p>\n * **Faster Cure Time:** DMAP can accelerate the cure time of coatings, adhesives, and sealants, increasing production throughput and reducing energy consumption.\n* **Improved Adhesion:** DMAP can enhance the adhesion of coatings and adhesives to various substrates, improving performance and durability.\n* **Enhanced Chemical Resistance:** DMAP can contribute to improved chemical resistance of coatings and elastomers, extending their service life in harsh environments.\n* **Lower VOC Content:** By promoting a more complete reaction and reducing the need for solvents, DMAP can help to reduce the VOC content of CASE products.<\/code><\/pre>\n\n\n\n| Property<\/th>\n | Traditional Catalyst (Tertiary Amine)<\/th>\n | DMAP Catalyst<\/th>\n | Improvement<\/th>\n<\/tr>\n<\/thead>\n | \n\n| Cure Time (min)<\/td>\n | 30 – 60<\/td>\n | 15 – 30<\/td>\n | Faster<\/td>\n<\/tr>\n | \n| Adhesion (MPa)<\/td>\n | 5 – 10<\/td>\n | 8 – 15<\/td>\n | Higher<\/td>\n<\/tr>\n | \n| VOC Content (g\/L)<\/td>\n | 100 – 200<\/td>\n | 50 – 100<\/td>\n | Lower<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n Green Chemistry Aspects of DMAP Utilization<\/strong><\/p>\n\n- Atom Economy and Waste Reduction<\/strong><\/li>\n<\/ul>\n
DMAP promotes the urethane reaction with high selectivity, minimizing the formation of undesirable side products. This leads to improved atom economy, meaning that a larger proportion of the reactants is incorporated into the desired product, reducing waste generation. The reduced formation of allophanates and biurets, which can negatively impact polyurethane properties, also minimizes the need for purification steps and further waste generation.<\/p>\n \n- Energy Efficiency and Process Optimization<\/strong><\/li>\n<\/ul>\n
DMAP’s high catalytic activity allows for faster reaction rates and lower reaction temperatures. This can lead to significant energy savings during polyurethane production. Furthermore, the improved reaction control achieved with DMAP allows for process optimization, such as reduced cycle times and improved product consistency, further enhancing energy efficiency.<\/p>\n \n- Safer Solvents and Reduced Toxicity<\/strong><\/li>\n<\/ul>\n
The enhanced reaction efficiency achieved with DMAP can reduce the need for solvents in polyurethane formulations. This is particularly important because many common solvents are VOCs and pose environmental and health hazards. By minimizing solvent usage, DMAP contributes to a safer and more sustainable polyurethane production process. Furthermore, while DMAP itself is not completely non-toxic (see "Challenges and Future Directions"), its lower volatility compared to many traditional amine catalysts contributes to reduced exposure and potential health risks.<\/p>\n Challenges and Future Directions<\/strong><\/p>\n\n- Cost Considerations<\/strong><\/li>\n<\/ul>\n
DMAP is generally more expensive than traditional tertiary amine catalysts. This can be a barrier to its widespread adoption, particularly in cost-sensitive applications. However, the higher catalytic activity of DMAP allows for lower catalyst loadings, which can partially offset the higher cost. Furthermore, the benefits of DMAP, such as reduced VOC emissions, improved product performance, and enhanced process efficiency, can justify the higher cost in many cases. Continued research and development efforts are focused on reducing the cost of DMAP production to make it more competitive with traditional catalysts.<\/p>\n \n- Potential Toxicity and Safety Concerns<\/strong><\/li>\n<\/ul>\n
While DMAP is generally considered less volatile than many tertiary amine catalysts, it is not completely non-toxic. It can cause skin and eye irritation, and inhalation of DMAP dust can cause respiratory irritation. Therefore, appropriate safety precautions, such as wearing gloves, safety glasses, and respiratory protection, should be taken when handling DMAP. Furthermore, the long-term health effects of exposure to DMAP are not fully understood, and further research is needed to assess its safety profile.<\/p>\n \n- Research and Development Opportunities<\/strong><\/li>\n<\/ul>\n
Several research and development opportunities exist to further enhance the role of DMAP in reducing VOC emissions for green chemistry:<\/p>\n * **Development of DMAP Derivatives:** Synthesizing DMAP derivatives with improved catalytic activity, selectivity, and reduced toxicity.\n* **Immobilization of DMAP:** Immobilizing DMAP on solid supports to create heterogeneous catalysts that can be easily recovered and reused, further reducing waste and improving process efficiency.\n* **Combination with Other Catalysts:** Combining DMAP with other catalysts, such as metal catalysts or enzymes, to create synergistic catalytic systems with enhanced performance and reduced VOC emissions.\n* **Application in Waterborne Polyurethane Systems:** Investigating the use of DMAP in waterborne polyurethane systems, which inherently have lower VOC content compared to solvent-based systems.\n* **Life Cycle Assessment:** Conducting life cycle assessments to comprehensively evaluate the environmental impact of using DMAP in polyurethane production, considering all stages from raw material extraction to end-of-life disposal.<\/code><\/pre>\nConclusion<\/strong><\/p>\nDMAP is a promising catalyst for reducing VOC emissions in polyurethane production, contributing to greener and more sustainable chemistry. Its high catalytic activity, selectivity, and lower volatility compared to traditional tertiary amine catalysts make it an attractive alternative for various polyurethane applications. By enhancing reaction rates, promoting isocyanate consumption, and influencing polyurethane microstructure, DMAP helps to minimize unreacted isocyanate, reduce blowing agent usage, and improve product performance, all of which contribute to lower VOC emissions. While challenges remain regarding cost and potential toxicity, ongoing research and development efforts are focused on addressing these issues and further enhancing the role of DMAP in sustainable polyurethane production. As the demand for environmentally friendly materials continues to grow, DMAP is poised to play an increasingly important role in the future of polyurethane chemistry. ♻️<\/p>\n References<\/strong><\/p>\n\n- Bock, H., et al. "DMAP-Catalyzed Polyurethane Synthesis: A Mechanistic Study." Journal of Polymer Science Part A: Polymer Chemistry<\/em> 45.15 (2007): 3319-3329.<\/li>\n
- Oertel, G., ed. Polyurethane Handbook<\/em>. 2nd ed. Hanser Gardner Publications, 1994.<\/li>\n
- Rand, L., and B. Thir. "The Chemistry and Applications of Polyurethanes." Journal of Macromolecular Science, Reviews in Macromolecular Chemistry<\/em> C14.1 (1976): 1-60.<\/li>\n
- Szycher, M. Szycher’s Handbook of Polyurethanes<\/em>. 2nd ed. CRC Press, 1999.<\/li>\n
- Ulrich, H. Introduction to Industrial Polymers<\/em>. 2nd ed. Hanser Publishers, 1993.<\/li>\n
- Wittcoff, H.A., et al. Industrial Organic Chemicals<\/em>. John Wiley & Sons, 2004.<\/li>\n
- Prokscha, H., et al. "New catalysts for polyurethane chemistry." Macromolecular Materials and Engineering<\/em> 289.3 (2004): 251-263.<\/li>\n
- Rosthauser, J.W., and K. Nachtkamp. "Water-Borne Polyurethanes." Advances in Urethane Science and Technology<\/em> 10 (1987): 121-162.<\/li>\n
- Woods, G. The ICI Polyurethanes Book<\/em>. 2nd ed. John Wiley & Sons, 1990.<\/li>\n
- Randall, D., and S. Lee. The Polyurethanes Book<\/em>. John Wiley & Sons, 2002.<\/li>\n
- US EPA. "Volatile Organic Compounds’ Impact on Indoor Air Quality." [No specific URL provided, but refer to EPA’s website for detailed information].<\/li>\n
- European Chemicals Agency (ECHA). Information on specific isocyanates and VOCs. [No specific URL provided, but refer to ECHA’s website for detailed information].<\/li>\n
- Zhang, Y., et al. "Influence of catalyst on the properties of rigid polyurethane foam." Journal of Applied Polymer Science<\/em> 130.2 (2013): 1200-1207.<\/li>\n
- Chen, L., et al. "DMAP-Catalyzed Synthesis of Polyurethanes with Reduced Isocyanate Emissions." Polymer Engineering & Science<\/em> 58.10 (2018): 1732-1739.<\/li>\n
- Li, W., et al. "Novel DMAP-Based Catalysts for Polyurethane Coatings with Enhanced Performance." Progress in Organic Coatings<\/em> 135 (2019): 187-195.<\/li>\n<\/ol>\n
(Note: This list provides examples and may need to be expanded and adjusted based on specific research and sources used).<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":" The Role of Polyurethane Catalyst DMAP in Reducing VOC …<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/59844"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=59844"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/59844\/revisions"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=59844"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=59844"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=59844"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
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