{"id":8625,"date":"2025-03-08T16:30:41","date_gmt":"2025-03-08T13:00:41","guid":{"rendered":"https:\/\/yektapajooh.com\/activator-for-use-in-phosphating-processes\/"},"modified":"2025-03-08T16:30:41","modified_gmt":"2025-03-08T13:00:41","slug":"activator-for-use-in-phosphating-processes","status":"publish","type":"post","link":"https:\/\/yektapajooh.com\/en\/activator-for-use-in-phosphating-processes\/","title":{"rendered":"Activator for Use in Phosphating Processes"},"content":{"rendered":"<h1><strong>Activator for Use in Phosphating Processes<\/strong><\/h1>\n<h2><strong>Introduction<\/strong><\/h2>\n<p>This document concerns a patent filed in Germany. The author intends to explain the application, background, and objectives of the invention and provides specific examples.<\/p>\n<p>U.S. Patent No. <strong>5,160,551<\/strong>, entitled <strong>\u201cActivator for Use in Phosphating Processes,\u201d<\/strong> was filed on April 17, 1991, by R\u00fcdiger Rhein, Dieter Jentsch, and Klaus-Werner Wittel of the Federal Republic of Germany, and assigned to Metallgesellschaft Aktiengesellschaft in Frankfurt.<\/p>\n<h2><strong>Summary of the Patent<\/strong><\/h2>\n<p>This patent relates to the development of an <strong>activating agent based on titanium(IV) phosphate<\/strong> for activating metal surfaces prior to zinc phosphating. The agent contains one or more copper compounds, with a titanium-to-copper weight ratio ranging from <strong>1:100 to 60:1<\/strong>. The composition may also contain additional components such as condensed phosphates, silicates, complexing agents, water-soluble organic polymers, thickeners, and surfactants.<\/p>\n<h2><strong>Application<\/strong><\/h2>\n<p>The activating agent is used to prepare aqueous activation baths for the treatment of surfaces made of <strong>iron, steel, galvanized steel, zinc-alloy-coated steel, aluminum-coated steel, and aluminum<\/strong> prior to zinc phosphating. These baths contain <strong>0.001\u20130.060 g\/L titanium, 0.020\u20131.2 g\/L orthophosphate (calculated as P\u2082O\u2085), and 0.001\u20130.1 g\/L copper<\/strong>. The alkali content is adjusted so that the bath pH is between <strong>7 and 11<\/strong>, preferably between <strong>7.5 and 10<\/strong>.<\/p>\n<p>The titanium(IV) phosphate-based activating agent designed for activating metal surfaces prior to zinc phosphating contains one or more copper compounds. The Ti:Cu weight ratio is between <strong>1:100 and 60:1<\/strong>. Optionally, the agent may also contain at least one of the following components: condensed phosphate, silicate, complexing agent, water-soluble organic polymer, thickener, and surfactant.<\/p>\n<p>This agent is used to prepare aqueous activation baths for activating iron, steel, galvanized steel, zinc-alloy-coated steel, aluminum-coated steel, and aluminum prior to zinc phosphating. These baths contain <strong>0.001\u20130.060 g\/L titanium, 0.020\u20131.2 g\/L orthophosphate (calculated as P\u2082O\u2085), and 0.001\u20130.1 g\/L copper<\/strong>. The alkali content is adjusted to maintain a pH between <strong>7 and 11<\/strong>, preferably between <strong>7.5 and 10<\/strong>.<\/p>\n<h2><strong>Title<\/strong><\/h2>\n<p><strong>Activator for Use in Phosphating Processes<\/strong><\/p>\n<h2><strong>Cross-Reference to Related Application<\/strong><\/h2>\n<p>This application is related to co-pending application No. <strong>07\/686,800<\/strong>, filed on April 17, 1991. The present invention relates to a titanium(IV) phosphate-based activating agent designed for activating metal surfaces prior to zinc phosphating. The invention also relates to a phosphating method in which this activator is used to prepare activation baths.<\/p>\n<h1><strong>Background of the Invention<\/strong><\/h1>\n<p>Zinc phosphate layers can be formed on various metal surfaces, such as iron, steel, zinc-alloy-coated steel, aluminum, or aluminum-coated steel, using zinc phosphate-based aqueous solutions. Phosphating solutions may contain, in addition to zinc and phosphoric acid, other cations and anions and are generally applied by spraying, immersion, or a combination of both. The resulting zinc phosphate coatings provide <strong>corrosion protection, improved paint adhesion, reduced friction, facilitation of cold-forming operations, and electrical insulation<\/strong>.<\/p>\n<p>The phosphating process involves several preparation stages. Cleaning the metal surfaces is particularly important and is usually performed using alkaline or acidic cleaners to remove oils, grease, oxides, and solid particles adhering to the metal surface. When mild alkaline cleaners are used, cleaning and surface activation may be combined; however, activation is generally performed as a separate step after cleaning.<\/p>\n<p>The purpose of activating the metal surface is to ensure the formation of a zinc phosphate layer with <strong>fine crystals in the shortest possible time<\/strong>. The effectiveness of an activating agent is determined by the minimum phosphating time required. The ability to form fine-crystalline zinc phosphate coatings can also be evaluated by coating weight or by scanning electron microscope micrographs.<\/p>\n<p>Titanium(IV) phosphate-based activating agents have produced satisfactory results in practice. Titanium(IV) phosphates are formed by reacting aqueous solutions of titanium(IV) salts with soluble phosphates or phosphoric acid. However, products with activating properties are obtained only under specific production conditions, which are described in detail in U.S. Patents Nos. <strong>2,310,239 and 2,456,947<\/strong>. Even when the reaction conditions remain constant, performance in application technology may vary from one batch to another.<\/p>\n<p>One disadvantage of using titanium(IV) phosphate-based activating agents is that <strong>distilled water must be used<\/strong> to prepare the activation baths, because alkaline-earth metal ions present in tap water can destabilize the activation baths. These ions may also enter the activation bath through used rinse water.<\/p>\n<p>To prevent the adverse effects of alkaline-earth metal ions and activation-bath instability, <strong>DE-A-37 31089<\/strong> proposed adding cation-exchange zeolites with primary particle diameters below 3 micrometers to the titanium phosphate activator. Alternatively, <strong>EP-8-180523<\/strong> proposed adding phosphonic acid to the activation bath as a complexing agent, thereby allowing industrial wastewater to be used for preparing the bath. In addition, the presence of phosphonic acid allegedly causes the zinc phosphate coating to have extremely fine crystallites.<\/p>\n<p>However, the use of phosphonic acids has serious disadvantages. Even at concentrations of only a few milligrams per liter, they can poison phosphating baths and render them unusable within a short period.<\/p>\n<p>The use of complexing agents in phosphating processes can improve the quality of zinc phosphate coatings and increase the efficiency of activation baths. However, adding these compounds may create environmental concerns because some of them are not readily biodegradable and may accumulate in the environment. Therefore, complexing agents must be selected and used with consideration of their environmental impact and process stability.<\/p>\n<h1><strong>\u201cObjects of the Invention\u201d<\/strong><\/h1>\n<p>One object of the invention is to provide a <strong>titanium(IV) phosphate-based activating agent<\/strong> that can be used to activate metal surfaces prior to zinc phosphating without the disadvantages of known activating agents, that can be produced easily, and that produces stable activation baths with a long service life when used to prepare such baths.<\/p>\n<p>Another object is to provide an improved activating agent that ensures the formation of <strong>fine-crystalline zinc phosphate coatings within a short period of time<\/strong>.<\/p>\n<p>Another object is to provide an <strong>improved phosphating method<\/strong>.<\/p>\n<h1><strong>Description of the Invention<\/strong><\/h1>\n<p>These and other objects, which will become apparent below, are achieved by an activating agent containing <strong>titanium(IV) phosphate and one or more copper compounds<\/strong>, with a titanium-to-copper weight ratio ranging from <strong>1:100 to 60:1<\/strong>. The copper content is adjusted by adding copper compounds, which significantly reduce the phosphating time to a minimum.<\/p>\n<p>Another result of adding copper is improved stability of the activation bath over a wide temperature range, together with very good activating properties. Almost all copper compounds can be used to introduce copper into the activating agent.<\/p>\n<p>According to another feature of the invention, the activating agent contains copper compounds introduced in the form of <strong>copper hydroxide, copper oxide hydrate, copper tartrate, copper nitrate, and\/or copper phosphate<\/strong>. Although copper sulfate or copper chloride may be used, they are not preferred.<\/p>\n<p>According to another feature of the invention, an activating agent is provided that additionally contains at least one of the following: <strong>condensed phosphates, silicates, complexing agents, water-soluble organic polymers, thickeners, and surfactants<\/strong>. When an activating agent containing such additional additives is used in an activation bath, several additional desirable properties are obtained.<\/p>\n<p>For example, adding condensed phosphate to the activating agent makes the resulting activation bath less susceptible to hardness-forming elements. A water-soluble organic polymer stabilizes the colloidal titanium(IV) phosphate dispersed in the activation bath and thereby significantly extends the service life of the activation bath. Surfactants reduce surface tension, allowing the titanium phosphate activator to adhere more strongly to the metal surface.<\/p>\n<p>According to another feature of the invention, the activating agent contains <strong>0.1\u20134 wt.% titanium phosphate<\/strong>, calculated as Ti.<\/p>\n<p>For the preparation of aqueous activation baths used to activate iron, steel, galvanized steel, zinc-alloy-coated steel, aluminum-coated steel, and aluminum prior to zinc phosphating, the activating agent is used so that the resulting activation bath contains:<\/p>\n<ul>\n<li><strong>0.001\u20130.060 g\/L Ti<\/strong><\/li>\n<li><strong>0.020\u20131.2 g\/L orthophosphate<\/strong>, calculated as P\u2082O\u2085<\/li>\n<li><strong>0.001\u20130.1 g\/L Cu<\/strong><\/li>\n<li>A pH of <strong>7\u201311<\/strong>, preferably <strong>7.5\u201310<\/strong><\/li>\n<\/ul>\n<p>Copper concentrations above <strong>0.1 g\/L<\/strong> should be avoided because they may interfere with the subsequent phosphating operation.<\/p>\n<p>Accordingly, the invention may also comprise an activating agent additionally containing at least one condensed phosphate, silicate, complexing agent, water-soluble organic polymer, thickener, or surfactant in an activation bath containing the following components:<\/p>\n<ul>\n<li>Up to <strong>1.2 g\/L condensed phosphate<\/strong>, calculated as P\u2082O\u2085<\/li>\n<li>Up to <strong>0.5 g\/L silicate<\/strong>, calculated as SiO\u2082<\/li>\n<li>Up to <strong>1.0 g\/L complexing agent<\/strong><\/li>\n<li>Up to <strong>0.1 g\/L water-soluble organic polymer<\/strong><\/li>\n<li>Up to <strong>0.1 g\/L thickener<\/strong><\/li>\n<li>Up to <strong>0.3 g\/L surfactant<\/strong><\/li>\n<\/ul>\n<p>Activating agents may be incorporated into ready-to-use aqueous alkaline cleaners or into liquid or solid aqueous concentrates used to formulate aqueous alkaline cleaning baths. Due to the ease of dilution, preparing an aqueous cleaning\/activator concentrate is particularly advantageous.<\/p>\n<p>An aqueous cleaner or cleaning concentrate is prepared by dissolving or mixing one or more compounds selected from the group consisting of carbonates, silicates, phosphates, borates, hydroxides, hydroxycarboxylic acids, and organic polymers, such as sodium bicarbonate (NaHCO\u2083), sodium carbonate (Na\u2082CO\u2083), sodium metasilicate (Na\u2082SiO\u2083), sodium disilicate (Na\u2082Si\u2082O\u2085), sodium water glass, disodium phosphate (Na\u2082HPO\u2084), sodium tripolyphosphate (Na\u2085P\u2083O\u2081\u2080), borax (Na\u2082B\u2084O\u2087\u00b710H\u2082O), sodium hydroxide, sodium gluconate, sodium heptonate, sodium citrate, the trisodium salt of nitrilotriacetic acid, condensation products of phenolsulfonic acid or naphthalenesulfonic acid with formaldehyde, or\u2014because of their better water solubility\u2014the corresponding potassium compounds.<\/p>\n<p>Aqueous alkaline cleaners and alkaline cleaning concentrates generally contain surfactants. Suitable surfactants may be anionic or nonionic, such as sodium alkylbenzene sulfonates, sodium alkyl sulfonates, alkylphenol polyethylene glycol ethers, alkylphenol polyethylene glycol-polypropylene glycol ethers, alkyl polyethylene glycol ethers, alkylamine polyethylene glycol compounds, or block copolymers of ethylene oxide and propylene oxide.<\/p>\n<p>When liquid aqueous cleaning concentrates are used, the surfactant content is approximately <strong>0.5\u201310 wt.%<\/strong>, preferably <strong>0.5\u20134 wt.%<\/strong>.<\/p>\n<p>To prevent the precipitation of insoluble and, where present, coarsely dispersed particles of the activating agent in an aqueous cleaning-activator concentrate, and to prevent phase separation of the surfactants in the concentrates due to salting-out effects, it is advantageous to add thickeners that may be selected from naturally occurring polymers.<\/p>\n<p>Suitable polymers include, for example, <strong>polypeptides such as gelatin<\/strong>, or <strong>polysaccharides such as starch, xanthan, and dextrin<\/strong>.<\/p>\n<p>When preparing concentrates of this type, it is advantageous to first completely dissolve the polymer in water and then add the other cleaning components. The surfactants are subsequently dissolved or finely dispersed by vigorous stirring. The activating agent is added at the end of the preparation process.<\/p>\n<p>When properly formulated, a liquid cleaning-activator concentrate can remain stable for several months at <strong>0\u201335\u00b0C<\/strong> and remain pumpable. Considering the solubility of the components, preparation method, and packaging and transportation costs, it is particularly advantageous to prepare a concentrate containing <strong>50\u201390 wt.%<\/strong>, preferably <strong>60\u201375 wt.% water<\/strong>.<\/p>\n<h1><strong>Specific Examples<\/strong><\/h1>\n<p>The invention will be described in greater detail in the following examples.<\/p>\n<h2><strong>Example 1<\/strong><\/h2>\n<p>Steel sheets of grade <strong>St 1405<\/strong> were processed according to the following procedure:<\/p>\n<ol>\n<li><strong>Cleaning<\/strong> \u2013 Immersion in a highly alkaline cleaner; 20 g\/L; 10 minutes; 70\u00b0C.<\/li>\n<li><strong>Rinsing<\/strong> \u2013 Cold water; 30 seconds.<\/li>\n<li><strong>Cleaning<\/strong> \u2013 Immersion in a mildly alkaline cleaner; 13 g\/L; 5 minutes; 60\u00b0C.<\/li>\n<li><strong>Rinsing<\/strong> \u2013 Cold water; 30 seconds.<\/li>\n<li><strong>Activation<\/strong> \u2013 Pretreatment with 1 g\/L activating agent; immersion for 30 seconds; 22\u00b0C.<\/li>\n<li><strong>Phosphating<\/strong> \u2013 1.2 g\/L Zn; 12.0 g\/L P\u2082O\u2085; 0.8 g\/L Mn; 0.8 g\/L Ni; 7 g\/L NO\u2083; 4.07 g\/L Na; 0.17 g\/L NaNO\u2082; 50\u00b0C; phosphating times of 3 and 6 minutes; immersion.<\/li>\n<li><strong>Rinsing<\/strong> \u2013 Cold water; 30 seconds.<\/li>\n<li><strong>Drying<\/strong> \u2013 With hot air.<\/li>\n<\/ol>\n<p>A total of <strong>six activating agents<\/strong> were produced and used to prepare the corresponding activation baths.<\/p>\n<h2><strong>Activating Agent 1<\/strong><\/h2>\n<p>To produce the activating agent according to the invention, <strong>3.27 kg of solid sodium hydroxide<\/strong> was dissolved in <strong>4.9 kg of water<\/strong>. After the solution had cooled, a solution of <strong>0.54 kg HTiF\u2086 (40 wt.%)<\/strong> and <strong>0.97 kg Ca(NO\u2083)\u2082\u00b74H\u2082O<\/strong> in <strong>4.36 kg of water<\/strong> was added.<\/p>\n<p>After the resulting slurry had cooled, a solution of <strong>4.91 kg H\u2083PO\u2084 (55 wt.% P\u2082O\u2085)<\/strong> in <strong>0.46 kg of water<\/strong> was added, ensuring that the temperature did not exceed <strong>45\u00b0C<\/strong>.<\/p>\n<p>After completion of the phosphoric acid addition, the temperature was slowly increased to <strong>70\u201390\u00b0C<\/strong>. This temperature was maintained for <strong>30 minutes<\/strong> to allow the activating agent to mature.<\/p>\n<p>Subsequently, an aqueous solution of <strong>216.67 g Cu(NO\u2083)\u2082\u00b73H\u2082O<\/strong> was uniformly dispersed into the slurry, and the slurry was dried. All mixing and maturation operations were carried out with stirring.<\/p>\n<h2><strong>Activating Agent 1a<\/strong><\/h2>\n<p>An activating agent was produced using the procedure described for Activating Agent 1, but <strong>without the addition of copper nitrate<\/strong>.<\/p>\n<h2><strong>Activating Agent 2<\/strong><\/h2>\n<p>To produce this activating agent, <strong>50 kg titanyl sulfate, 375 kg solid NaOH, 580 kg phosphoric acid (55 wt.% P\u2082O\u2085), 159 kg solid Na\u2082CO\u2083, and 170 kg water<\/strong> were kneaded together, and copper phosphate was added in an amount sufficient to obtain a copper concentration of <strong>2 wt.%<\/strong>.<\/p>\n<h2><strong>Activating Agent 2a<\/strong><\/h2>\n<p>An activating agent with a composition similar to Activating Agent 2 was produced, but <strong>without copper phosphate<\/strong>.<\/p>\n<h2><strong>Activating Agent 3<\/strong><\/h2>\n<p>To produce Activating Agent 3, a relatively large amount of <strong>maleic acid anhydride copolymer<\/strong> was added to Activating Agent 1 so that the resulting activation bath contained <strong>10 mg\/L<\/strong> of the polymer.<\/p>\n<h2><strong>Activating Agent 4<\/strong><\/h2>\n<p>This activating agent was produced from Activating Agent 1 by adding a quantity of surfactant such that the subsequently prepared activation bath contained a surfactant concentration of <strong>0.3 g\/L<\/strong>.<\/p>\n<p>The coating provided after phosphating times of <strong>3 and 6 minutes<\/strong> was determined. The coating was evaluated based on the proportion of the metal surface covered by a continuous zinc phosphate coating. Evaluation was performed through visual inspection.<\/p>\n<p>The phosphate coating weight was determined gravimetrically, together with the minimum phosphating time. The minimum phosphating time is the minimum time required to form a continuous phosphate coating.<\/p>\n<p>The crystallinity of the phosphate coatings was determined from scanning electron microscope micrographs at <strong>2000\u00d7 magnification<\/strong>.<\/p>\n<p>The results obtained for each case, including the metal surface coverage after phosphating times of 3 and 6 minutes, respectively, the minimum phosphating time, coating weight, and service life of the phosphating baths in days, are summarized in the following table.<\/p>\n<p><a href=\"https:\/\/yektapajooh.com\/wp-content\/uploads\/2025\/03\/test-1-300x117.png\">Image<\/a><\/p>\n<p>The above table clearly demonstrates that the use of the activating agent according to the invention, as shown in Examples 1, 2, 3, and 4, results in a high and nearly complete coverage of the metal surface even after a phosphating time of only <strong>3 minutes<\/strong>, allowing short processing times to be used in the subsequent phosphating stage. The phosphate coating weight is well within the normal range.<\/p>\n<p>The results obtained using Activating Agents 3 and 4 demonstrate that the addition of <strong>maleic acid anhydride copolymer and a surfactant<\/strong> significantly increases the service life of the activation bath while maintaining short minimum phosphating times compared with Activating Agent 1.<\/p>\n<p>Examination by scanning electron microscopy showed that the phosphate layers formed when the activating agents according to the invention were used were <strong>fine-grained<\/strong>.<\/p>\n<h1><strong>Claims<\/strong><\/h1>\n<p><strong>1.<\/strong> An activating composition comprising an activating agent for activating metal surfaces prior to zinc phosphating, comprising titanium(IV) phosphate and containing at least one copper compound, wherein the activating agent has a Ti:Cu weight ratio of <strong>1:100 to 60:1<\/strong>, and wherein the composition contains <strong>0.001\u20130.060 g\/L TiO<\/strong>, <strong>0.020\u20131.2 g\/L orthophosphate<\/strong> calculated as P\u2082O\u2085, and <strong>0.001\u20130.1 g\/L Cu<\/strong>, together with sufficient alkali to provide a pH of <strong>7\u201311<\/strong>.<\/p>\n<p><strong>2.<\/strong> The activating agent defined in Claim 1, wherein the copper compound is selected from the group consisting of <strong>copper hydroxide, copper oxide hydrate, copper tartrate, copper nitrate, and copper phosphate<\/strong>.<\/p>\n<p><strong>3.<\/strong> The activating agent defined in Claim 1, further comprising at least one of a <strong>condensed phosphate, silicate, complexing agent, water-soluble organic polymer, thickener, or surfactant<\/strong>.<\/p>\n<p><strong>4.<\/strong> The activating agent defined in Claim 2, containing <strong>0.1\u20134 wt.% titanium phosphate<\/strong>, calculated as Ti.<\/p>\n<p><strong>5.<\/strong> An activating composition according to Claim 1 comprising a <strong>ready-to-use aqueous alkaline cleaner or an aqueous alkaline cleaning concentrate or solid<\/strong>.<\/p>\n<p><strong>6.<\/strong> The use defined in Claim 5, wherein the pH is <strong>7.5\u201310<\/strong>.<\/p>\n<p><strong>7.<\/strong> The activating composition according to Claim 3, containing:<\/p>\n<ul>\n<li>Up to <strong>1.2 g\/L condensed phosphate<\/strong>, calculated as P\u2082O\u2085<\/li>\n<li>Up to <strong>0.5 g\/L silicate<\/strong>, calculated as SiO\u2082<\/li>\n<li>Up to <strong>1.0 g\/L complexing agent<\/strong><\/li>\n<li>Up to <strong>0.1 g\/L water-soluble organic polymer<\/strong><\/li>\n<li>Up to <strong>0.1 g\/L thickener<\/strong><\/li>\n<li>Up to <strong>0.3 g\/L surfactant<\/strong><\/li>\n<\/ul>\n<p><strong>8.<\/strong> A phosphating method comprising the following steps:<\/p>\n<p><strong>(a)<\/strong> Forming an aqueous activating solution containing:<\/p>\n<ul>\n<li><strong>0.001\u20130.060 g\/L Ti<\/strong><\/li>\n<li><strong>0.020\u20131.2 g\/L orthophosphate<\/strong>, calculated as P\u2082O\u2085<\/li>\n<li><strong>0.001\u20130.1 g\/L Cu<\/strong><\/li>\n<li>Sufficient alkali to provide a pH of <strong>7\u201311<\/strong><\/li>\n<\/ul>\n<p><strong>(b)<\/strong> Treating the metal surface with the aqueous activating solution; and<\/p>\n<p><strong>(c)<\/strong> Bringing the metal surface into contact with a <strong>zinc phosphating bath<\/strong>.<\/p>\n<p><strong>9.<\/strong> The method defined in Claim 8, wherein the solution contains:<\/p>\n<ul>\n<li>Up to <strong>1.2 g\/L condensed phosphate<\/strong>, calculated as P\u2082O\u2085<\/li>\n<li>Up to <strong>0.5 g\/L silicate<\/strong>, calculated as SiO\u2082<\/li>\n<li>Up to <strong>1.0 g\/L complexing agent<\/strong><\/li>\n<li>Up to <strong>0.1 g\/L water-soluble organic polymer<\/strong><\/li>\n<li>Up to <strong>0.1 g\/L thickener<\/strong><\/li>\n<li>Up to <strong>0.3 g\/L surfactant<\/strong><\/li>\n<\/ul>\n<p><strong>10.<\/strong> The method defined in Claim 8, wherein the pH of the solution is adjusted to <strong>7.5\u201310<\/strong>.<\/p>\n<p><strong>11.<\/strong> The composition according to Claim 1, wherein the metal surface is <strong>iron, steel, galvanized steel, zinc-alloy-coated steel, aluminum-coated steel, or aluminum<\/strong>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Activator for Use in Phosphating Processes Introduction This document concerns a patent filed in Germany. The author intends to explain the application, background, and objectives of the invention and provides specific examples. U.S. Patent No. 5,160,551, entitled \u201cActivator for Use in Phosphating Processes,\u201d was filed on April 17, 1991, by R\u00fcdiger Rhein, Dieter Jentsch, and [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":8627,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[207,201],"tags":[],"class_list":["post-8625","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-phosphating-products","category-scientific-and-educational"],"_links":{"self":[{"href":"https:\/\/yektapajooh.com\/en\/wp-json\/wp\/v2\/posts\/8625","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/yektapajooh.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/yektapajooh.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/yektapajooh.com\/en\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/yektapajooh.com\/en\/wp-json\/wp\/v2\/comments?post=8625"}],"version-history":[{"count":0,"href":"https:\/\/yektapajooh.com\/en\/wp-json\/wp\/v2\/posts\/8625\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/yektapajooh.com\/en\/wp-json\/wp\/v2\/media\/8627"}],"wp:attachment":[{"href":"https:\/\/yektapajooh.com\/en\/wp-json\/wp\/v2\/media?parent=8625"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/yektapajooh.com\/en\/wp-json\/wp\/v2\/categories?post=8625"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/yektapajooh.com\/en\/wp-json\/wp\/v2\/tags?post=8625"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}