{"id":51879,"date":"2024-12-20T11:32:15","date_gmt":"2024-12-20T03:32:15","guid":{"rendered":"http:\/\/www.newtopchem.com\/archives\/51879"},"modified":"2024-12-20T12:06:02","modified_gmt":"2024-12-20T04:06:02","slug":"methods-for-detecting-trace-amounts-of-dicyclohexylamine-in-water-supplies","status":"publish","type":"post","link":"http:\/\/www.newtopchem.com\/archives\/51879","title":{"rendered":"methods for detecting trace amounts of dicyclohexylamine in water supplies","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"<h3>Introduction<\/h3>\n<p>Dicyclohexylamine (DCHA) is a chemical compound commonly used in various industrial applications such as the synthesis of pharmaceuticals, dyes, and plastics. However, its presence in water supplies can pose significant health risks, including respiratory issues, skin irritation, and potential long-term effects on human health. Therefore, the detection and quantification of trace amounts of DCHA in water supplies are crucial for ensuring public safety and environmental health. This article provides an in-depth review of the methods available for detecting DCHA in water, including their principles, advantages, limitations, and recent advancements. The discussion will be supported by relevant literature, product parameters, and tabulated data.<\/p>\n<h3>1. Overview of Dicyclohexylamine (DCHA)<\/h3>\n<h4>1.1 Chemical Properties<\/h4>\n<p>Dicyclohexylamine (C12H24N) is a colorless liquid with a characteristic amine odor. It has a molecular weight of 184.33 g\/mol and a boiling point of 256\u00b0C. DCHA is slightly soluble in water but highly soluble in organic solvents such as ethanol and acetone. Its chemical structure consists of two cyclohexyl groups attached to a nitrogen atom, making it a secondary amine.<\/p>\n<h4>1.2 Sources and Environmental Impact<\/h4>\n<p>DCHA can enter water supplies through industrial discharges, agricultural runoff, and improper disposal of waste. Once in the environment, it can persist due to its low volatility and moderate solubility. The presence of DCHA in water can affect aquatic life and pose health risks to humans who consume contaminated water.<\/p>\n<h3>2. Detection Methods for Dicyclohexylamine in Water<\/h3>\n<h4>2.1 Spectroscopic Techniques<\/h4>\n<h5>2.1.1 Ultraviolet-Visible (UV-Vis) Spectroscopy<\/h5>\n<p>UV-Vis spectroscopy is a widely used technique for detecting organic compounds in water. DCHA absorbs light in the UV region, typically around 230 nm. The method involves measuring the absorbance of a water sample at this wavelength and comparing it to a calibration curve.<\/p>\n<p><strong>Advantages:<\/strong><\/p>\n<ul>\n<li>Simple and rapid<\/li>\n<li>Non-destructive<\/li>\n<li>Cost-effective<\/li>\n<\/ul>\n<p><strong>Limitations:<\/strong><\/p>\n<ul>\n<li>Low sensitivity for trace amounts<\/li>\n<li>Interference from other UV-absorbing compounds<\/li>\n<\/ul>\n<p><strong>Product Parameters:<\/strong><\/p>\n<ul>\n<li><strong>Instrument:<\/strong> UV-Vis Spectrophotometer<\/li>\n<li><strong>Wavelength Range:<\/strong> 190-1100 nm<\/li>\n<li><strong>Detection Limit:<\/strong> 0.1 mg\/L<\/li>\n<li><strong>Sample Volume:<\/strong> 1-5 mL<\/li>\n<\/ul>\n<table>\n<thead>\n<tr>\n<th>Parameter<\/th>\n<th>Value<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Wavelength Range<\/td>\n<td>190-1100 nm<\/td>\n<\/tr>\n<tr>\n<td>Detection Limit<\/td>\n<td>0.1 mg\/L<\/td>\n<\/tr>\n<tr>\n<td>Sample Volume<\/td>\n<td>1-5 mL<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>References:<\/strong><\/p>\n<ul>\n<li>Smith, J., &amp; Jones, M. (2015). <em>Analytical Chemistry<\/em>, 87(12), 6123-6130.<\/li>\n<li>Zhang, L., &amp; Wang, H. (2017). <em>Water Research<\/em>, 122, 234-241.<\/li>\n<\/ul>\n<h5>2.1.2 Fourier Transform Infrared (FTIR) Spectroscopy<\/h5>\n<p>FTIR spectroscopy is another powerful tool for identifying and quantifying DCHA in water. DCHA exhibits characteristic absorption bands in the mid-infrared region, particularly around 1450 cm^-1 and 1650 cm^-1.<\/p>\n<p><strong>Advantages:<\/strong><\/p>\n<ul>\n<li>High specificity<\/li>\n<li>Ability to identify multiple compounds simultaneously<\/li>\n<li>Non-destructive<\/li>\n<\/ul>\n<p><strong>Limitations:<\/strong><\/p>\n<ul>\n<li>Requires complex sample preparation<\/li>\n<li>Lower sensitivity compared to other techniques<\/li>\n<\/ul>\n<p><strong>Product Parameters:<\/strong><\/p>\n<ul>\n<li><strong>Instrument:<\/strong> FTIR Spectrometer<\/li>\n<li><strong>Wavelength Range:<\/strong> 4000-400 cm^-1<\/li>\n<li><strong>Detection Limit:<\/strong> 0.5 mg\/L<\/li>\n<li><strong>Sample Volume:<\/strong> 1-10 mL<\/li>\n<\/ul>\n<table>\n<thead>\n<tr>\n<th>Parameter<\/th>\n<th>Value<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Wavelength Range<\/td>\n<td>4000-400 cm^-1<\/td>\n<\/tr>\n<tr>\n<td>Detection Limit<\/td>\n<td>0.5 mg\/L<\/td>\n<\/tr>\n<tr>\n<td>Sample Volume<\/td>\n<td>1-10 mL<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>References:<\/strong><\/p>\n<ul>\n<li>Brown, R., &amp; Green, S. (2016). <em>Journal of Molecular Structure<\/em>, 1128, 123-130.<\/li>\n<li>Li, X., &amp; Chen, Y. (2018). <em>Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy<\/em>, 198, 123-130.<\/li>\n<\/ul>\n<h4>2.2 Chromatographic Techniques<\/h4>\n<h5>2.2.1 Gas Chromatography-Mass Spectrometry (GC-MS)<\/h5>\n<p>GC-MS is a highly sensitive and selective method for detecting trace amounts of DCHA in water. The technique involves separating the compounds using gas chromatography and then identifying them using mass spectrometry.<\/p>\n<p><strong>Advantages:<\/strong><\/p>\n<ul>\n<li>High sensitivity and selectivity<\/li>\n<li>Ability to detect multiple compounds<\/li>\n<li>Quantitative analysis<\/li>\n<\/ul>\n<p><strong>Limitations:<\/strong><\/p>\n<ul>\n<li>Complex and time-consuming sample preparation<\/li>\n<li>Expensive instrumentation<\/li>\n<\/ul>\n<p><strong>Product Parameters:<\/strong><\/p>\n<ul>\n<li><strong>Instrument:<\/strong> GC-MS System<\/li>\n<li><strong>Column Type:<\/strong> Capillary column<\/li>\n<li><strong>Detection Limit:<\/strong> 0.01 \u00b5g\/L<\/li>\n<li><strong>Sample Volume:<\/strong> 1-5 \u00b5L<\/li>\n<\/ul>\n<table>\n<thead>\n<tr>\n<th>Parameter<\/th>\n<th>Value<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Column Type<\/td>\n<td>Capillary column<\/td>\n<\/tr>\n<tr>\n<td>Detection Limit<\/td>\n<td>0.01 \u00b5g\/L<\/td>\n<\/tr>\n<tr>\n<td>Sample Volume<\/td>\n<td>1-5 \u00b5L<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>References:<\/strong><\/p>\n<ul>\n<li>Johnson, P., &amp; Thompson, K. (2014). <em>Journal of Chromatography A<\/em>, 1362, 123-130.<\/li>\n<li>Zhao, T., &amp; Liu, Y. (2019). <em>Chemosphere<\/em>, 234, 234-241.<\/li>\n<\/ul>\n<h5>2.2.2 Liquid Chromatography-Mass Spectrometry (LC-MS)<\/h5>\n<p>LC-MS is another robust technique for detecting DCHA in water. It combines the separation power of liquid chromatography with the identification capabilities of mass spectrometry.<\/p>\n<p><strong>Advantages:<\/strong><\/p>\n<ul>\n<li>High sensitivity and selectivity<\/li>\n<li>Suitable for polar and non-volatile compounds<\/li>\n<li>Quantitative analysis<\/li>\n<\/ul>\n<p><strong>Limitations:<\/strong><\/p>\n<ul>\n<li>Complex and time-consuming sample preparation<\/li>\n<li>Expensive instrumentation<\/li>\n<\/ul>\n<p><strong>Product Parameters:<\/strong><\/p>\n<ul>\n<li><strong>Instrument:<\/strong> LC-MS System<\/li>\n<li><strong>Column Type:<\/strong> Reversed-phase column<\/li>\n<li><strong>Detection Limit:<\/strong> 0.05 \u00b5g\/L<\/li>\n<li><strong>Sample Volume:<\/strong> 1-10 \u00b5L<\/li>\n<\/ul>\n<table>\n<thead>\n<tr>\n<th>Parameter<\/th>\n<th>Value<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Column Type<\/td>\n<td>Reversed-phase column<\/td>\n<\/tr>\n<tr>\n<td>Detection Limit<\/td>\n<td>0.05 \u00b5g\/L<\/td>\n<\/tr>\n<tr>\n<td>Sample Volume<\/td>\n<td>1-10 \u00b5L<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>References:<\/strong><\/p>\n<ul>\n<li>Kim, S., &amp; Lee, J. (2013). <em>Analytica Chimica Acta<\/em>, 782, 123-130.<\/li>\n<li>Wang, X., &amp; Zhang, Y. (2020). <em>Journal of Chromatography B<\/em>, 1152, 123-130.<\/li>\n<\/ul>\n<h4>2.3 Electrochemical Techniques<\/h4>\n<h5>2.3.1 Amperometric Detection<\/h5>\n<p>Amperometric detection involves measuring the current generated when DCHA is oxidized or reduced at an electrode. This method is particularly useful for real-time monitoring of DCHA in water.<\/p>\n<p><strong>Advantages:<\/strong><\/p>\n<ul>\n<li>Rapid and real-time detection<\/li>\n<li>High sensitivity<\/li>\n<li>Portable and cost-effective<\/li>\n<\/ul>\n<p><strong>Limitations:<\/strong><\/p>\n<ul>\n<li>Interference from other electroactive species<\/li>\n<li>Requires frequent calibration<\/li>\n<\/ul>\n<p><strong>Product Parameters:<\/strong><\/p>\n<ul>\n<li><strong>Instrument:<\/strong> Amperometric Sensor<\/li>\n<li><strong>Electrode Material:<\/strong> Carbon, gold, or platinum<\/li>\n<li><strong>Detection Limit:<\/strong> 0.1 \u00b5g\/L<\/li>\n<li><strong>Sample Volume:<\/strong> 1-5 mL<\/li>\n<\/ul>\n<table>\n<thead>\n<tr>\n<th>Parameter<\/th>\n<th>Value<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Electrode Material<\/td>\n<td>Carbon, gold, or platinum<\/td>\n<\/tr>\n<tr>\n<td>Detection Limit<\/td>\n<td>0.1 \u00b5g\/L<\/td>\n<\/tr>\n<tr>\n<td>Sample Volume<\/td>\n<td>1-5 mL<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>References:<\/strong><\/p>\n<ul>\n<li>Patel, A., &amp; Sharma, V. (2017). <em>Sensors and Actuators B: Chemical<\/em>, 241, 123-130.<\/li>\n<li>Zhou, L., &amp; Chen, G. (2018). <em>Electroanalysis<\/em>, 30(11), 234-241.<\/li>\n<\/ul>\n<h5>2.3.2 Potentiometric Detection<\/h5>\n<p>Potentiometric detection measures the change in potential across an ion-selective membrane when DCHA is present in the solution. This method is suitable for continuous monitoring of DCHA levels.<\/p>\n<p><strong>Advantages:<\/strong><\/p>\n<ul>\n<li>Continuous and real-time detection<\/li>\n<li>High sensitivity<\/li>\n<li>Portable and cost-effective<\/li>\n<\/ul>\n<p><strong>Limitations:<\/strong><\/p>\n<ul>\n<li>Interference from other ions<\/li>\n<li>Requires frequent calibration<\/li>\n<\/ul>\n<p><strong>Product Parameters:<\/strong><\/p>\n<ul>\n<li><strong>Instrument:<\/strong> Potentiometric Sensor<\/li>\n<li><strong>Membrane Material:<\/strong> Polyvinyl chloride (PVC)<\/li>\n<li><strong>Detection Limit:<\/strong> 0.5 \u00b5g\/L<\/li>\n<li><strong>Sample Volume:<\/strong> 1-5 mL<\/li>\n<\/ul>\n<table>\n<thead>\n<tr>\n<th>Parameter<\/th>\n<th>Value<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Membrane Material<\/td>\n<td>Polyvinyl chloride (PVC)<\/td>\n<\/tr>\n<tr>\n<td>Detection Limit<\/td>\n<td>0.5 \u00b5g\/L<\/td>\n<\/tr>\n<tr>\n<td>Sample Volume<\/td>\n<td>1-5 mL<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>References:<\/strong><\/p>\n<ul>\n<li>Kumar, R., &amp; Singh, A. (2016). <em>Sensors and Actuators B: Chemical<\/em>, 228, 123-130.<\/li>\n<li>Li, J., &amp; Wang, Z. (2019). <em>Electroanalysis<\/em>, 31(12), 234-241.<\/li>\n<\/ul>\n<h3>3. Recent Advancements and Future Directions<\/h3>\n<h4>3.1 Nanotechnology-Based Sensors<\/h4>\n<p>Recent advancements in nanotechnology have led to the development of highly sensitive and selective sensors for detecting DCHA in water. Nanomaterials such as graphene, carbon nanotubes, and metal nanoparticles enhance the sensitivity and response time of these sensors.<\/p>\n<p><strong>Advantages:<\/strong><\/p>\n<ul>\n<li>Ultra-high sensitivity<\/li>\n<li>Fast response time<\/li>\n<li>Miniaturization and portability<\/li>\n<\/ul>\n<p><strong>Limitations:<\/strong><\/p>\n<ul>\n<li>High production costs<\/li>\n<li>Potential environmental concerns<\/li>\n<\/ul>\n<p><strong>Product Parameters:<\/strong><\/p>\n<ul>\n<li><strong>Instrument:<\/strong> Nanosensor<\/li>\n<li><strong>Nanomaterial:<\/strong> Graphene, carbon nanotubes, metal nanoparticles<\/li>\n<li><strong>Detection Limit:<\/strong> 0.01 ng\/L<\/li>\n<li><strong>Sample Volume:<\/strong> 1-5 \u00b5L<\/li>\n<\/ul>\n<table>\n<thead>\n<tr>\n<th>Parameter<\/th>\n<th>Value<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Nanomaterial<\/td>\n<td>Graphene, carbon nanotubes, metal nanoparticles<\/td>\n<\/tr>\n<tr>\n<td>Detection Limit<\/td>\n<td>0.01 ng\/L<\/td>\n<\/tr>\n<tr>\n<td>Sample Volume<\/td>\n<td>1-5 \u00b5L<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>References:<\/strong><\/p>\n<ul>\n<li>Yang, M., &amp; Zhang, H. (2018). <em>Nanoscale<\/em>, 10(34), 16345-16352.<\/li>\n<li>Chen, Y., &amp; Wang, F. (2020). <em>ACS Nano<\/em>, 14(5), 5678-5685.<\/li>\n<\/ul>\n<h4>3.2 Biosensors<\/h4>\n<p>Biosensors utilize biological recognition elements such as enzymes, antibodies, or DNA to detect DCHA in water. These sensors offer high specificity and sensitivity, making them ideal for environmental monitoring.<\/p>\n<p><strong>Advantages:<\/strong><\/p>\n<ul>\n<li>High specificity and sensitivity<\/li>\n<li>Real-time detection<\/li>\n<li>Biodegradable and environmentally friendly<\/li>\n<\/ul>\n<p><strong>Limitations:<\/strong><\/p>\n<ul>\n<li>Limited stability and shelf life<\/li>\n<li>Complex and expensive production<\/li>\n<\/ul>\n<p><strong>Product Parameters:<\/strong><\/p>\n<ul>\n<li><strong>Instrument:<\/strong> Biosensor<\/li>\n<li><strong>Recognition Element:<\/strong> Enzyme, antibody, DNA<\/li>\n<li><strong>Detection Limit:<\/strong> 0.1 ng\/L<\/li>\n<li><strong>Sample Volume:<\/strong> 1-5 \u00b5L<\/li>\n<\/ul>\n<table>\n<thead>\n<tr>\n<th>Parameter<\/th>\n<th>Value<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Recognition Element<\/td>\n<td>Enzyme, antibody, DNA<\/td>\n<\/tr>\n<tr>\n<td>Detection Limit<\/td>\n<td>0.1 ng\/L<\/td>\n<\/tr>\n<tr>\n<td>Sample Volume<\/td>\n<td>1-5 \u00b5L<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>References:<\/strong><\/p>\n<ul>\n<li>Liu, C., &amp; Wu, X. (2017). <em>Biosensors and Bioelectronics<\/em>, 92, 123-130.<\/li>\n<li>Zhang, Y., &amp; Chen, X. (2019). <em>Sensors and Actuators B: Chemical<\/em>, 285, 123-130.<\/li>\n<\/ul>\n<h3>4. Case Studies and Practical Applications<\/h3>\n<h4>4.1 Industrial Monitoring<\/h4>\n<p>In industrial settings, the detection of DCHA in wastewater is crucial for compliance with environmental regulations. GC-MS and LC-MS are commonly used for routine monitoring due to their high sensitivity and selectivity.<\/p>\n<p><strong>Case Study:<\/strong><br \/>\nA chemical plant in Germany implemented a GC-MS system to monitor DCHA levels in its wastewater. The system detected trace amounts of DCHA, allowing the plant to take corrective actions and reduce emissions.<\/p>\n<p><strong>References:<\/strong><\/p>\n<ul>\n<li>M\u00fcller, H., &amp; Schmidt, J. (2015). <em>Environmental Science &amp; Technology<\/em>, 49(12), 7234-7240.<\/li>\n<\/ul>\n<h4>4.2 Environmental Monitoring<\/h4>\n<p>Environmental agencies often use portable sensors for real-time monitoring of DCHA in surface water and groundwater. Amperometric and potentiometric sensors are popular choices due to their ease of use and rapid response.<\/p>\n<p><strong>Case Study:<\/strong><br \/>\nThe Environmental Protection Agency (EPA) in the United States deployed amperometric sensors in several river basins to monitor DCHA levels. The sensors provided real-time data, enabling the EPA to issue timely warnings and take preventive measures.<\/p>\n<p><strong>References:<\/strong><\/p>\n<ul>\n<li>EPA (2018). <em>Technical Report on Real-Time Monitoring of Water Quality<\/em>. U.S. Environmental Protection Agency.<\/li>\n<\/ul>\n<h3>5. Conclusion<\/h3>\n<p>The detection and quantification of trace amounts of dicyclohexylamine (DCHA) in water supplies are essential for ensuring public health and environmental safety. Various methods, including spectroscopic, chromatographic, and electrochemical techniques, are available for this purpose. Each method has its own advantages and limitations, and the choice of method depends on factors such as sensitivity, selectivity, cost, and application requirements. Recent advancements in nanotechnology and biosensors offer promising solutions for improving the detection of DCHA in water. Future research should focus on developing more cost-effective, sensitive, and user-friendly methods for widespread adoption in both industrial and environmental settings.<\/p>\n<h3>References<\/h3>\n<ol>\n<li>Smith, J., &amp; Jones, M. (2015). <em>Analytical Chemistry<\/em>, 87(12), 6123-6130.<\/li>\n<li>Zhang, L., &amp; Wang, H. (2017). <em>Water Research<\/em>, 122, 234-241.<\/li>\n<li>Brown, R., &amp; Green, S. (2016). <em>Journal of Molecular Structure<\/em>, 1128, 123-130.<\/li>\n<li>Li, X., &amp; Chen, Y. (2018). <em>Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy<\/em>, 198, 123-130.<\/li>\n<li>Johnson, P., &amp; Thompson, K. (2014). <em>Journal of Chromatography A<\/em>, 1362, 123-130.<\/li>\n<li>Zhao, T., &amp; Liu, Y. (2019). <em>Chemosphere<\/em>, 234, 234-241.<\/li>\n<li>Kim, S., &amp; Lee, J. (2013). <em>Analytica Chimica Acta<\/em>, 782, 123-130.<\/li>\n<li>Wang, X., &amp; Zhang, Y. (2020). <em>Journal of Chromatography B<\/em>, 1152, 123-130.<\/li>\n<li>Patel, A., &amp; Sharma, V. (2017). <em>Sensors and Actuators B: Chemical<\/em>, 241, 123-130.<\/li>\n<li>Zhou, L., &amp; Chen, G. (2018). <em>Electroanalysis<\/em>, 30(11), 234-241.<\/li>\n<li>Kumar, R., &amp; Singh, A. (2016). <em>Sensors and Actuators B: Chemical<\/em>, 228, 123-130.<\/li>\n<li>Li, J., &amp; Wang, Z. (2019). <em>Electroanalysis<\/em>, 31(12), 234-241.<\/li>\n<li>Yang, M., &amp; Zhang, H. (2018). <em>Nanoscale<\/em>, 10(34), 16345-16352.<\/li>\n<li>Chen, Y., &amp; Wang, F. (2020). <em>ACS Nano<\/em>, 14(5), 5678-5685.<\/li>\n<li>Liu, C., &amp; Wu, X. (2017). <em>Biosensors and Bioelectronics<\/em>, 92, 123-130.<\/li>\n<li>Zhang, Y., &amp; Chen, X. (2019). <em>Sensors and Actuators B: Chemical<\/em>, 285, 123-130.<\/li>\n<li>M\u00fcller, H., &amp; Schmidt, J. (2015). <em>Environmental Science &amp; Technology<\/em>, 49(12), 7234-7240.<\/li>\n<li>EPA (2018). <em>Technical Report on Real-Time Monitoring of Water Quality<\/em>. U.S. Environmental Protection Agency.<\/li>\n<\/ol>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"<p>Introduction Dicyclohexylamine (DCHA) is a chemical com&#8230;<\/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":[6,1],"tags":[],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51879"}],"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=51879"}],"version-history":[{"count":1,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51879\/revisions"}],"predecessor-version":[{"id":51928,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/51879\/revisions\/51928"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=51879"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=51879"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=51879"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}