Tech Ingredients
Blending multi-sized barium sulfate nanoparticles into an acrylic binder creates a coating that reflects 99% of solar energy and emits mid-infrared heat, driving outdoor metal 3 °C below ambient air without power.
AI-assisted summary of Revolutionary Paint: How to Make Surfaces Stay Cool in the Sun — original source. Check the original for full context.
Source published:
Key ideas
- A specialized radiative cooling paint formulated with dense barium sulfate nanoparticles and an acrylic binder achieves passive, sub-ambient cooling (~3 °C below ambient temperature) in direct sunlight. (46:47)
- Barium sulfate acts as both a near-lossless solar scatterer (>99% visible reflectance via multi-crystal scattering) and a microscopic infrared nano-antenna (>96% emissivity around the 10 µm thermal window). (3:00)
- Reaching maximum packing density requires multimodal particle sizing synthesized across varying temperatures (0 °C for ~10 nm up to 95 °C for several hundred nm) to overcome the ~64% geometric density limit of uniform spheres. (13:06)
- Outdoor trials in November sunlight demonstrated that the custom paint stayed 3 °C below ambient air, whereas bare aluminum ran 20 °C hotter and commercial white paint sat 8–10 °C above ambient. (46:47)
Detailed notes
## Background This guide was published on YouTube by Tech Ingredients on March 3, 2023. Serving as a detailed follow-up to a previous project that showcased a custom liquid cooling panel, the video provides comprehensive instructions on formulating and applying the specialized, ultra-reflective radiative cooling paint that enables sub-ambient thermal performance.
## TL;DR The video outlines the chemical synthesis, physical principles, and application techniques required to fabricate a passive radiative cooling 'super paint' using barium sulfate and an acrylic PMMA binder. By utilizing multimodal particle sizing and controlling precipitation conditions, the coating reflects over 99% of solar radiation while behaving as a microscopic nano-antenna that emits heat into the infrared atmospheric window. Applied in roughly 27 thin passes to reach a 0.5 mm thickness on an acid-etched aluminum substrate, the coating demonstrates true daytime sub-ambient passive refrigeration. Real-world outdoor testing under direct sunlight proves the treated panel stays approximately 3 °C cooler than ambient air, heavily outperforming both bare aluminum and commercial white paint.
## Atmosphere & style The presentation carries the warm, highly instructional atmosphere of an advanced DIY garage laboratory, blending rigorous chemical theory with practical workshop resourcefulness. The host delivers the tutorial with engaging enthusiasm, accessible dry humor, and a genuine delight in science, even casually sipping medical barium sulfate suspension on camera to prove its non-toxicity. The pace transitions from meticulous bench-scale chemistry into an authentic, slightly gritty workshop endurance test as the host and cameraman grind through hours of repeated spray passes, culminating in an outdoors, data-driven payoff that feels both technically satisfying and deeply validating.
## Bulletin - [46:47](https://www.youtube.com/watch?v=dNs_kNilSjk&t=2807s) A specialized radiative cooling paint formulated with dense barium sulfate nanoparticles and an acrylic binder achieves passive, sub-ambient cooling (~3 °C below ambient temperature) in direct sunlight. - [03:00](https://www.youtube.com/watch?v=dNs_kNilSjk&t=180s) Barium sulfate acts as both a near-lossless solar scatterer (>99% visible reflectance via multi-crystal scattering) and a microscopic infrared nano-antenna (>96% emissivity around the 10 µm thermal window). - [13:06](https://www.youtube.com/watch?v=dNs_kNilSjk&t=786s) Reaching maximum packing density requires multimodal particle sizing synthesized across varying temperatures (0 °C for ~10 nm up to 95 °C for several hundred nm) to overcome the ~64% geometric density limit of uniform spheres. - [46:47](https://www.youtube.com/watch?v=dNs_kNilSjk&t=2807s) Outdoor trials in November sunlight demonstrated that the custom paint stayed 3 °C below ambient air, whereas bare aluminum ran 20 °C hotter and commercial white paint sat 8–10 °C above ambient.
## Key takeaways - [00:00](https://www.youtube.com/watch?v=dNs_kNilSjk&t=0s) Passive radiative cooling operates with an effectively infinite energy efficiency ratio (EER) because heat rejection requires zero ongoing power input. - [01:14](https://www.youtube.com/watch?v=dNs_kNilSjk&t=74s) Daytime passive cooling requires an engineered surface that simultaneously reflects over 99% of incoming solar irradiance while emitting over 96% in the mid-infrared (~10 µm) window. - [03:00](https://www.youtube.com/watch?v=dNs_kNilSjk&t=180s) Barium sulfate is biologically inert, inexpensive, and features an electronic vibrational structure that naturally resonates at room-temperature thermal infrared frequencies. - [04:36](https://www.youtube.com/watch?v=dNs_kNilSjk&t=276s) The optical scattering mechanism of barium sulfate functions like snow, using internal refraction and external facet reflection across non-absorbing crystals to bounce virtually all sunlight away. - [08:06](https://www.youtube.com/watch?v=dNs_kNilSjk&t=486s) Uncontrolled precipitation yields large, jagged crystalline aggregates; adding an EDTA surfactant chelates barium ions to force uniform, smooth, spherical nanoparticle formation. - [09:37](https://www.youtube.com/watch?v=dNs_kNilSjk&t=577s) Using sodium sulfate rather than sulfuric acid as the sulfate donor avoids corrosive hydrochloric acid byproducts, yielding safe, dilute table salt solution. - [09:37](https://www.youtube.com/watch?v=dNs_kNilSjk&t=577s) Allowing the precipitated suspension to rest overnight improves particle quality through Ostwald ripening, smoothing and polishing the crystal faces naturally. - [13:06](https://www.youtube.com/watch?v=dNs_kNilSjk&t=786s) Multimodal densification using batches produced at 0 °C, 30 °C, 60 °C, and 95 °C fills interstitial voids between particles, pushing solids loading far beyond the ~64% limit of uniform spheres. - [17:53](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1073s) Standard epoxies and polyurethanes fail as binders because their lack of volatile components forces high resin ratios; polymethyl methacrylate (PMMA) dissolved in dimethylformamide (DMF) allows ultra-high solids loading. - [17:53](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1073s) Slow-evaporating solvents like DMF are required to build a 0.5 mm thick film across 20 to 30 individual spray coats without clogging guns or producing stringy polymer strands. - [26:40](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1600s) A relatively low molecular weight acrylic resin (~80,000–100,000 MW) heated to ~70 °C provides the ideal balance of solubility, wetting, and mechanical binding. - [30:32](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1832s) Targeting a fluid viscosity of 100 to 150 centipoise (7–8 seconds in a Zahn #3 cup) ensures optimal flow and atomization for HVLP spray application. - [33:15](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1995s) Aluminum substrates require a strict three-stage surface preparation protocol—solvent degreasing, mechanical sanding, and acid-etch priming—to defeat the rapidly reforming aluminum oxide layer. - [37:13](https://www.youtube.com/watch?v=dNs_kNilSjk&t=2233s) Recoating must occur within a specific window when the surface turns matte and dry to the touch but retains faint solvent traces to ensure strong interlaminar acrylic bonding without vapor blistering. - [37:13](https://www.youtube.com/watch?v=dNs_kNilSjk&t=2233s) Diffuse scattering from a dead-matte paint finish reflects the exact same percentage of solar energy as a mirror-like specular gloss finish. - [46:47](https://www.youtube.com/watch?v=dNs_kNilSjk&t=2807s) In live outdoor testing, the 27-coat barium sulfate panel remained roughly 3 °C below ambient outdoor air, outperforming commercial super white paint by over 11 °C.
## Detailed walkthrough ### [00:00](https://www.youtube.com/watch?v=dNs_kNilSjk&t=0s) Radiative Cooling and the Concept of Super Paint
In a previous project, the channel demonstrated an engineered cooling device capable of chilling circulating water below the ambient air temperature simply by radiating thermal energy out into the surrounding environment. While that panel utilized just a couple of watts of electrical power to pump and circulate the fluid, the actual thermodynamic cooling mechanism was entirely passive. Because it expends zero energy to perform the heat extraction itself, its effective energy efficiency ratio (EER) is virtually infinite.
The enabling breakthrough behind this thermal panel is a specialized surface coating or "super paint" engineered to radiate heat while defying daytime solar loading. Because this coating can be manufactured from straightforward, relatively inexpensive ingredients, the host sets out to explain both the foundational physics governing how it works and how anyone can fabricate it in a home laboratory. As the host notes regarding the initial prototype's validation: “Now if you're interested in this technology you might want to take a look back at that video because we go through the engineering we build the device we test it and it really worked.”
- Power consumption of the fluid pump: A couple of watts - Effective Energy Efficiency Ratio (EER): Infinite (passive heat rejection) - Goal: Formulate an inexpensive, DIY-accessible high-performance radiative cooling coating
---
[01:14](https://www.youtube.com/watch?v=dNs_kNilSjk&t=74s) The Physics of Emissivity and Solar Rejection
All physical objects emit electromagnetic radiation based on their temperature. At typical terrestrial, body, and room temperatures, this thermal glow peaks within the infrared spectrum at roughly 10 microns (10,000 nanometers). The effectiveness with which a physical surface radiates this thermal energy is defined as its emissivity. Common everyday substances—such as human skin, textiles, timber, concrete, plastics, and conventional commercial paints—typically exhibit thermal emissivity ratings ranging between 75% and 90%. However, maximizing radiative cooling requires driving that emissivity percentage as high as possible.
Operating such a passive radiative system under direct sunlight introduces an opposing technical challenge: rejecting the massive influx of daytime solar energy, which can deposit up to 1,000 watts (1 kilowatt) per square meter onto an exposed surface. Surfaces must simultaneously exhibit near-perfect reflectance across the solar spectrum while maximizing emissivity in the mid-infrared. Historically, achieving both properties simultaneously required alternating multi-layer dielectric optical thin films—similar to laser optics—manufactured using multi-million-dollar chemical vapor deposition (CVD) vacuum chambers with painfully slow throughput. Highlighting the breakthrough alternative, the host explains: “So there's been a lot of recent interest focused on this one material that performs both functions better than any other known substance it's widely available it's non-toxic and it's cheap barium sulfate.”
```mermaid flowchart TD accTitle: Radiative Cooling Mechanism Dual Balance accDescr: Diagram illustrating the simultaneous solar reflection and infrared heat emission requirements. subgraph SolarInput["Incident Solar Radiation"] Sun["Sun (~1,000 W/m²)"] -->|"Broadband visible & near-IR"| Surf["Surface Coating"] end subgraph OpticalBehavior["Dual-Mode Performance"] Surf -->|"Reflection (>99%)"| SpaceReflect["Reflected into Sky / Space"] Surf -->|"Thermal Emissivity (>96% at ~10 µm)"| IRRadiate["Radiated into Infrared Window"] end ```
---
[03:00](https://www.youtube.com/watch?v=dNs_kNilSjk&t=180s) Barium Sulfate: From Medical Milkshakes to Nano-Antennas
Barium sulfate ($\text{BaSO}_4$) is mined globally at a scale of roughly 10 million tons per year in the form of the mineral barite. While raw barite often resembles quartz and displays streaks of pink, blue, or green due to various mineral impurities, chemically pure barium sulfate is entirely colorless and optically crystal clear. It is also exceptionally benign biologically; despite barium being a heavy metal, barium sulfate's insolubility makes it safe enough for clinical use.
For decades, radiologists and gastroenterologists have utilized barium sulfate suspensions as a drinkable contrast agent. Because barium has a high atomic weight, it is radiopaque, showing up crisply on plain flat-plate x-rays to delineate the internal morphology of the gastrointestinal tract, revealing ulcers, diverticula, and tumors. To prove its safety, the host drinks a dose from an actual medical diagnostic cup on camera, deadpanning: “It's literally safe to drink.” After tasting it, he chuckles and notes that “it's not bad even comes in strawberry.”
Beyond its non-toxic profile, the crystal lattice of barium sulfate exhibits an electronic vibrational structure that naturally resonates at the exact frequencies corresponding to room-temperature thermal vibrations. As a result, every individual crystal behaves like a microscopic nano-antenna, radiating thermal energy straight out into the environment with an emissivity exceeding 96%.
- Global mining production of barite: Approximately 10 million tons per year - Medical application: Diagnostic radiopaque contrast agent for gastrointestinal x-rays - Resonant thermal emission: Operates as a nano-antenna in the mid-infrared (~10 µm) with >96% efficiency
---
[04:36](https://www.youtube.com/watch?v=dNs_kNilSjk&t=276s) The Optical Scattering Mechanism: The Snow Effect
The reason barium sulfate exhibits world-class solar reflectance comes down to its sheer optical clarity, operating on the exact physical mechanism that makes snow one of the most reflective substances on Earth. Liquid water is clear, yet when transformed into millions of crystalline snowflakes, it scatters incoming light in all directions without absorbing it.
When incoming sunlight strikes an optically pure crystal of barium sulfate or a snowflake, a fraction of the photon flux reflects directly off the crystal facets and scatters away, while another fraction enters the crystal, refracts through it, and exits in scattered directions. Light scattered backward toward the source constitutes direct reflection. Meanwhile, light refracted deeper into the bulk material encounters another crystal boundary, repeating the refraction and scattering sequence indefinitely. Because the material itself does not absorb visible wavelengths, the scattering process is essentially lossless, progressively bleeding light back toward the sky until virtually all of it escapes. Pure, dry barium sulfate powder achieved via this multi-scattering mechanism boasts a total visible reflectivity exceeding 99%.
---
[05:48](https://www.youtube.com/watch?v=dNs_kNilSjk&t=348s) Basic Double Displacement Synthesis of Barium Sulfate
To synthesize barium sulfate in the laboratory, one can mimic industrial pathways where mined barite is first converted into water-soluble barium chloride ($\text{BaCl}_2$) using heat and carbon. The host prepares a 0.2 molar ($0.2\text{ M}$) aqueous solution of barium chloride. He clarifies the concept of molarity for the audience by noting that barium chloride has a molecular weight of approximately 208 g/mol; dissolving 208 grams in one liter produces a $1\text{ M}$ solution, so a $0.2\text{ M}$ concentration corresponds to a one-fifth molar strength.
```mermaid flowchart LR accTitle: Precipitation Double Displacement Reaction accDescr: Flowchart of the reaction between barium chloride and sulfuric acid producing barium sulfate and hydrochloric acid. subgraph Reactants["Aqueous Reactants"] A["BaCl₂ (aq)"] B["H₂SO₄ (aq)"] end subgraph Products["Products"] C["BaSO₄ (s) ↓ (Precipitate)"] D["2 HCl (aq)"] end A --> E["Double Displacement"] B --> E E --> C E --> D ```
Pouring the clear barium chloride solution into glass Petri dishes, the host introduces a sulfate donor using a dropper filled with 20% sulfuric acid ($\text{H}_2\text{SO}_4$). The instant the acid droplets hit the liquid, opaque white clouds billow outward through a classic double displacement reaction:
$$\text{BaCl}_2 + \text{H}_2\text{SO}_4 \rightarrow \text{BaSO}_4\downarrow + 2\text{HCl}$$
Barium ions bind with sulfate ions to form an insoluble barium sulfate precipitate that drifts down to the bottom, leaving aqueous hydrochloric acid behind. Delighting in the vivid reaction, the host smiles and exclaims: “I love this chemistry is fun something to show your kids.”
---
[08:06](https://www.youtube.com/watch?v=dNs_kNilSjk&t=486s) Controlling Particle Morphology with EDTA Surfactants
Although the basic sulfuric acid precipitation creates real barium sulfate, the host warns that the resulting material is unsuitable for ultra-reflective radiative cooling paint. The rapid, uncontrolled precipitation spawns irregular, multi-micron-sized crystalline aggregates resembling microscopic jagged boulders. These large, uneven particles pack together poorly, leaving voids that degrade solar scattering and optical reflectivity. Achieving maximum performance requires dense particle packing, which demands smooth, spherical, nanometer-scale particles spanning a curated distribution of sizes.
The standard chemical technique for tailoring particle geometry is adding a surfactant (surface-active agent) to moderate crystallization. The host credits another YouTube creator, saying: “And that's exactly what NighthawkInLight did several months ago when he was covering this technology if you're interested in the subject take a look at his video it's very well done and it's interesting I think you'll like it.”
A chelating surfactant such as ethylenediaminetetraacetic acid (EDTA) temporarily bonds with and coordinates the barium ions in solution. When nucleation begins, the EDTA shields the growing seeds and carefully meters the rate at which free barium ions reach the crystal face. This controlled growth suppresses rapid jagged clustering, forcing the precipitate to assemble into uniform, round, nanometer-scale spheres.
- Goal: Nanometer-scale, smooth, spherical particles with varied size distribution for dense packing - Problem with unmoderated reaction: Generates large, jagged multi-micron aggregates - Solution: Introduce EDTA to sequester and meter barium ion availability during precipitation
---
[09:37](https://www.youtube.com/watch?v=dNs_kNilSjk&t=577s) Nanopowder Precipitation, Centrifugation, and Particle Aging
To execute the controlled synthesis, the host mixes 0.2 molar barium chloride with an equimolar amount of EDTA surfactant. Because EDTA has a molecular weight roughly 50% greater than barium chloride, the recipe requires approximately 1.5 times the weight of EDTA relative to the barium chloride salt. Rather than using sulfuric acid—which would yield corrosive hydrochloric acid as a byproduct—the host uses sodium sulfate ($\text{Na}_2\text{SO}_4$) as the sulfate donor. This substitution yields harmless, dilute table salt ($\text{NaCl}$) in solution, making downstream handling far safer and simpler.
$$\text{BaCl}_2 + \text{Na}_2\text{SO}_4 \xrightarrow{\text{EDTA}} \text{BaSO}_4\downarrow + 2\text{NaCl}$$
Upon pouring the sodium sulfate into the stirred barium chloride/EDTA mixture, the clear liquid flashes into a silky, milky white suspension of barium sulfate nanopowder within seconds. To collect the solids, a magnetic wand secures the stir bar inside the beaker while the suspension is decanted into 50 mL centrifuge tubes, carefully balancing the weights across rotor buckets.
The tubes are spun in an Amazon-sourced benchtop centrifuge at 4,000 RPM for several minutes to compress the nanopowder into a dense pellet. The host points out with amusement that this particular centrifuge was purchased for around $300 from Amazon's "foodie" section—a department catering to modernist cuisine and molecular gastronomy. Although limited to 4,000 RPM, it can spin up to 300 milliliters per batch, providing rapid turnaround.
The host reveals a final culinary parallel: the raw nanopowder suspension actually improves if left to sit prior to centrifugation. When left undisturbed overnight, the particles undergo Ostwald ripening and surface restructuring, rounding off remaining asperities. As the host remarks: “And in keeping with the food theme what's another interesting fact about this suspension is that it ages like fine wine if before I did this step we simply turned out the lights and came back the next day overnight the suspension will allow the barium sulfate to slightly rearrange and the particles become even smoother even rounder and almost polished so it doesn't add any more work but if you're a little more patient you're going to get a little bit better result and that's exactly what he found.”
- EDTA to barium chloride mass ratio: ~1.5:1 (equimolar concentration) - Preferred sulfate donor: Sodium sulfate (leaves dilute $\text{NaCl}$ instead of $\text{HCl}$) - Centrifuge specs: 4,000 RPM, 300 mL maximum batch capacity, cost ~$300 - Ripening behavior: Overnight resting allows crystalline surfaces to smooth out and polish naturally
[13:06](https://www.youtube.com/watch?v=dNs_kNilSjk&t=786s) The Principle of Densification and Particle Sizing
Controlling the precipitation reaction using EDTA yields much smaller, spherical nanoparticles that noticeably enhance paint performance, but reaching the true state of the art requires taking advantage of densification. This principle, which also gives ultra-high-performance concrete its strength, governs how particles pack inside a fixed volume. If a container is filled with uniform spheres, simply pouring them in yields roughly 60% solids loading, and even the tightest, neatest packing maxes out at approximately 64% due to the unavoidable geometric voids between them. The size of the particles does not change this ratio; smaller uniform spheres leave smaller voids, but proportionally more of them. To pack beyond that physical limit, medium-sized particles must be introduced to occupy the voids between the larger spheres, followed by even tinier nanoparticles to pack the remaining gaps between the medium ones, asymptotically approaching 100% solids loading.
```mermaid flowchart TD accTitle: Multimodal Densification and Synthesis Process accDescr: Step-by-step process of producing multi-sized barium sulfate nanoparticles at different temperatures and compounding them into paint.
subgraph Synthesis["1. Temperature-Controlled Batches"] T0["0°C Batch: ~10 nm"] T30["30°C Batch: Intermediate"] T60["60°C Batch: Intermediate"] T95["95°C Batch: Several 100 nm"] end
subgraph Processing["2. Separation & Drying"] Cent["Centrifuge & Decant"] Dry["Oven Dry at 100°C–150°C"] end
subgraph Compounding["3. Paint Formulation"] Blend["Blend Multi-Size Powders"] Mix["Disperse in DMF + PMMA Binder"] end
T0 --> Cent T30 --> Cent T60 --> Cent T95 --> Cent Cent --> Dry Dry --> Blend Blend --> Mix ```
Because the barium chloride and sodium sulfate reaction is highly temperature-dependent, tuning the temperature directly tunes the particle diameter. Executing the synthesis near 0°C produces uniform, spherical barium sulfate nanoparticles around 10 nanometers across. Running the reaction near 95°C yields smooth nanoparticles measuring several hundred nanometers. By producing four separate batches—at 0°C, 30°C, 60°C, and 95°C—and blending them together, one creates a diversified particle distribution engineered for ultra-high-density loading. As the presenter explains: “now if we want to get to the actual state of the art the highest possible performance that anybody's been able to achieve we have to kick this thing up one more not and to do so we have to take advantage of a principle called densification”.
- Uniform particle packing density limit: ~60% poured, ~64% optimally packed. - Bimodal and multimodal distributions fill interstitial voids, pushing density toward theoretical maximums. - Reaction temperatures: 0°C (~10 nm particles), 30°C, 60°C, and 95°C (several hundred nm particles).
---
[15:46](https://www.youtube.com/watch?v=dNs_kNilSjk&t=946s) Harvesting and Drying the Barium Sulfate Nano Powder
After spinning down the synthesis mixture in the centrifuge, the barium sulfate settles into a firm white pellet at the base of the tubes, leaving the clear supernatant liquid above. Rather than cleaning out the tube after every single spin, the supernatant is simply decanted off, and fresh reaction solution can be poured directly over the existing pellet to run another cycle. Stacking multiple runs inside the same centrifuge tube saves substantial cleanup time before reaching diminishing returns.
Once the tube holds a sufficient accumulation of material, a stirring rod is used to extract the dense barium sulfate paste. The paste is spread onto a plate and dried in an oven set between 100°C and 150°C for several hours, leaving behind a fine, dry nano powder. This cycle is repeated across each temperature run, after which all the fractions are combined into a master blend. The presenter quips to the audience about the resulting fine white powder: “and when you're done you mix everything together and you have your white powder and no comment no jokes in the comment section this this really is barium sulfate”.
- Supernatant is poured off, leaving the concentrated barium sulfate pellet behind. - Centrifuge tubes can be refilled and spun repeatedly to accumulate larger pellets per tube. - Drying parameters: 100°C to 150°C for 2 hours in an oven.
---
[17:53](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1073s) Choosing the Binder and the Solvent: Acrylic and Dimethylformamide
Transforming the dry powder into paint requires a binder, but standard high-end coatings like two-part epoxy or polyurethane resin systems fail in this role. Because epoxies and polyurethanes contain virtually no volatile components, the ultra-dense powder quickly turns into an unworkable paste and then a stiff putty long before achieving the necessary solids loading. Adding extra resin to thin it out is unacceptable because no resin matches the optical properties of barium sulfate; maximizing performance demands minimizing binder content. The solution is polymethyl methacrylate (PMMA) acrylic resin dissolved in a volatile solvent. With an evaporative solvent, the liquid volume can be adjusted arbitrarily to achieve the exact viscosity needed for spreading or spray application, after which the solvent fully evaporates, leaving behind only the minimum polymer needed to bind the particles together.
The choice of solvent is equally critical. Dimethylformamide (DMF) performs best chemically, but it carries two major drawbacks: an unpleasant fishy odor reminiscent of dissecting frogs, and a very slow evaporation rate. Standard paint solvents like acetone, methyl ethyl ketone (MEK), and toluene smell comparatively pleasant and fruity, but they evaporate far too fast. Fast-evaporating solvents cause the high-solids mixture to gum up during application, and running them through a paint gun results in stringy messes that look like cotton candy or chopped fiberglass. Slow evaporation is mandatory because the coating relies purely on backscattering rather than opacifiers or pigments, necessitating 20 to 30 individual coats to reach a total film build of roughly 0.5 mm (5 to 10 times thicker than standard paint). Defending this heavy application schedule against skeptical trade painters, the presenter emphasizes: “this system is completely dependent on scattering and so you need a thick enough build so that all the light gets scattered back toward the source rather than get through and be absorbed by the substrate so you need a build thickness about a half a millimeter thick which is 5 to 10 times as thick as a typical spray of paint or stain”.
| Solvent Candidate | Evaporation Speed | Odor Profile | Spray / Application Behavior | |:--- |:--- |:--- |:--- | | **Dimethylformamide (DMF)** | Slow | Foul, fishy (similar to biological specimen preservative) | Allows uniform leveling; permits building 20–30 coats without clogging | | **Acetone / MEK / Toluene** | Very Fast | Pungent, sweet, fruity, perfumy | Gums up rapidly; produces stringy "cotton candy" or chop-gun-like strands from sprayers |
---
[21:27](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1287s) Paint Formulation, Equipment Hacks, and Sourcing Nano Powders
Before compounding the paint, a key chemical ratio must be observed: the addition of sodium sulfate to barium chloride requires equimolar amounts. If a reaction uses half the volume of sodium sulfate solution relative to the barium chloride, the sodium sulfate must be mixed at twice the molar concentration (for instance, a 0.4 M sodium sulfate solution paired with a 0.2 M barium chloride solution). When scaling up from laboratory beakers to multi-liter batches intended for whole roofs or astronomical observatories, standard lab hotplates become impractical. A KitchenAid stand mixer serves as an ideal bulk mixer, but because KitchenAid discontinued their heated mixing bowl attachment, a DIY alternative is required: eight 12-volt, 12-watt self-adhesive flexible polyimide heater strips wired to the exterior base of the metal mixing bowl provide roughly 100 watts of heating power, easily elevating the mixture to the target 70°C.
For the demonstration batch, 130 grams of dimethylformamide is weighed out and placed on a magnetic stirring plate, followed by 80 grams of dry barium sulfate nano powder. Because fine nano powders easily become airborne during handling, wearing a protective respirator mask is essential. The barium sulfate does not dissolve in DMF; rather, the magnetic stir bar physically shears and disperses aggregates and clumps formed during drying and transport to produce a silky, uniform suspension. Preparing nano powders from scratch is time-consuming, but commercial alternatives exist: Airtech Pvt. Ltd. in India sells bulk nano powder for under $4,000 per ton, and a test sample performed nearly as well as laboratory-synthesized powder. Alternatively, US Nano in Texas provides consistently high-grade nano powders with fast domestic delivery, though at a significantly higher cost of roughly $300 per kilogram. Regarding the dispersion process, the presenter notes: “what we're doing is we're using the mixing bar to sort of beat up and break up any kind of lumps or clumps that might have formed during storage or Transportation or drying and and we want as even and smooth a distribution throughout the liquid as possible”.
- Stoichiometric balance: Equimolar reagent quantities (e.g., half volume of 0.4 M $\text{Na}_2\text{SO}_4$ to 1 volume of 0.2 M $\text{BaCl}_2$). - Mixer modification: 8 flexible polyimide heater strips (12 V, 12 W each; ~100 W total) affixed to a stainless steel mixer bowl to reach ~70°C. - Batch ratio demonstrated: 130 g dimethylformamide (DMF) to 80 g blended barium sulfate nano powder. - Commercial suppliers: Airtech Pvt. Ltd. (<$4,000/ton) vs. US Nano (~$300/kg).
[25:40](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1540s) Mixing the Barium Sulfate Suspension
The presenter begins by letting the barium sulfate powder mix into the solvent on the magnetic stir plate. While the mixture can be stirred for as long as desired without damaging it, standard practice is to let it run for 20 to 30 minutes at approximately 300 RPM using a 50 mm stir bar. For a larger batch using the overhead mixer, running the same duration at a low speed yields an equally uniform, even dispersion.
```mermaid flowchart TD accTitle: Barium Sulfate and PMMA Dispersion Workflow accDescr: Step-by-step process of mixing barium sulfate powder into solvent, adding PMMA beads, and dissolving them under heat.
subgraph Prep ["1. Initial Dispersion"] A["BaSO4 in Solvent"] --> B["Stir 20–30 min @ 300 RPM<br/>(50 mm stir bar)"] B --> C["Break up soft powder lumps"] end
subgraph Dissolution ["2. Polymer Addition & Heating"] C --> D["Slowly add 14 g PMMA beads"] D --> E["Heat to ~70 °C on hot plate"] E --> F["Manual stirring as viscosity climbs"] end
subgraph Quality ["3. Final Adjustment"] F --> G["Weigh container to find lost solvent"] G --> H["Top off solvent to reach target viscosity"] end ```
As the powder blends into the vortex, small lumps appear on the surface. The presenter clarifies that simple magnetic stirring cannot break apart hard aggregate crystals that form during raw chemical synthesis, but it easily breaks down softer, clumping powder fragments. The stir plate is left to run for about half an hour to complete this initial wetting and de-agglomeration stage.
[26:40](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1600s) Adding PMMA and Polymer Molecular Weight
Once the barium sulfate is well-suspended, it is time to add the polymer binder: 14 grams of polymethyl methacrylate (PMMA). Because these are 200-micron beads rather than a fine nano-powder, a respirator mask is not required for this step. The host explains that PMMA is a polymer made up of varying chain lengths, with molecular weights ranging from roughly 10,000 to several million. Higher molecular weight versions provide superior thermal and structural properties—the kind used to make rigid sheets like Lucite and Plexiglas—but they are exceptionally difficult to dissolve in mild solvents.
For paint formulation, a relatively low molecular weight resin (around 80,000 MW) is ideal. The specific product shown is Elvacite 2028, manufactured by Lucite International and distributed in the United States by Mitsubishi Chemical. While inexpensive per pound, it is typically sold in commercial 55 lb bags. The team obtained their supply by reaching out directly with phone calls and emails to request a sample, prompting the host to joke: “Like the man said, politics is the ultimate science.” For viewers purchasing retail quantities, PolySciences sells a comparable product called PMMA 100, which designates an approximate molecular weight of 100,000.
The resin beads must be sprinkled into the stirring vortex very slowly. Dumping the entire measure in at once would cause the beads to fuse into a single rubbery lump: > “I'm adding this very, very slowly even though if I were just to dump this right in the container it would eventually dissolve, we'd end up with a gumball sort of flopping around inside of here and the reduced surface area would actually slow down the dissolution so by going slower we're actually going to be done faster.”
[28:40](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1720s) Heating, Viscosity Evolution, and Solvent Compensation
With the PMMA slowly added, the hot plate is turned on to bring the mixture up to an ultimate target of roughly 70 °C. The dial setting is not critical, so long as the solution reaches temperature. Initially, the suspension appears slightly grayish and translucent rather than brilliant white. This is an optical effect caused by the un-dissolved, translucent polymer beads swirling in the liquid. As the beads dissolve, they form a clear syrup resin that wets and binds the barium sulfate, causing the liquid to turn noticeably whiter and thicker.
Eventually, the rising viscosity overwhelms the magnetic stir bar, causing it to decouple and freeze up. While an overhead motorized mixer would power right through, on the stir plate one must switch to manual agitation with a glass stirring rod or a temperature probe.
The host shares a critical bench-chemistry tip for maintaining consistency when working with volatile solvents: > “Whenever you're doing any kind of a synthesis that involves a solvent, before you get started weigh all of your individual components—the beaker, the stirring bar, the stirring rod, a spoon, anything that you might use—weigh them, write them down and put them in your back pocket because when you do the synthesis, depending on the temperature of the room, the chemicals that that you're using, how long you stir it, you're going to lose a little bit of that solvent and you don't know exactly what it's going to be, but at the end when you add up all those weights and you find that you're down, say, 5 grams, it's easy enough to just put a little bit more solvent in there, bring yourself up to the same viscosity each time so it makes it very repeatable.”
[30:32](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1832s) Measuring Viscosity with a Zahn Cup
After the stir bar "gives up the ghost," stirring continues by hand until the temperature probe reads 70–72 °C and the polymer completely dissolves. The target fluid viscosity is between 100 and 150 centipoise (cP)—roughly 100 to 150 times thicker than water, visually resembling a texture midway between light and heavy cream.
To take the guesswork out of the formulation, especially for beginners, viscosity should be measured with an efflux cup such as a Ford/Wagner cup or a Zahn cup:
| Measurement Tool / Spec | Description & Procedure | |:--- |:--- | | **Instrument Used** | Zahn #3 cup (a calibrated 44 mL cup with a precision orifice in the base) | | **Measurement Procedure** | Submerge cup fully into liquid; lift vertically out while starting a stopwatch; stop the timer the moment the continuous stream breaks into individual droplets | | **Target Zahn #3 Time** | **7 to 8 seconds** (corresponds to ~100–150 cP) | | **Spraying Performance** | Delivers optimal "Goldilocks" flow for high-volume low-pressure (HVLP) spray guns | | **Storage & Shelf Life** | Indefinite storage in an airtight jar; re-stir or agitate prior to spraying to eliminate stratification |
[33:15](https://www.youtube.com/watch?v=dNs_kNilSjk&t=1995s) Aluminum Surface Preparation: Cleaning, Sanding, and Etching
To coat the radiant cooling panel, the operation moves from the lab bench to a large warehouse. Painting raw aluminum presents notorious adhesion challenges that require meticulous three-step surface preparation before applying any paint or structural epoxy:
```mermaid flowchart LR accTitle: Aluminum Surface Preparation Process accDescr: Three sequential steps for preparing raw aluminum: degreasing, sanding, and chemical etching.
A["1. Degrease"] -->|"Acetone / Brake Cleaner<br/>Wipe until paper is clean"| B["2. Mechanical Sanding"] B -->|"150-grit palm sander<br/>Creates tooth, removes debris"| C["3. Chemical Etch"] C -->|"Acid etch primer<br/>Lifts Al2O3, deposits Zn/Fe"| D["Ready for Coating"] ```
1. **Degreasing:** Raw mill aluminum is coated in processing oils and grease. Using a disposable paper towel wetted with a grease-cutting solvent like acetone or automotive brake cleaner, the plate is wiped repeatedly until the towel comes away spotless. Sanding without degreasing first would simply grind the oil into the metal, creating a contaminated slurry. 2. **Mechanical Sanding:** The panel is abraded using an orbital palm sander loaded with 150-grit sandpaper. Sanding expands the surface area and imparts mechanical "tooth" for the coating to grip. 3. **Overcoming the Oxide Layer:** Aluminum is chemically aggressive; bare metal reacts with atmospheric oxygen within milliseconds, forming a microscopic layer of aluminum oxide ($Al_2O_3$). The host compares this passive oxide layer to “the flour on a pizza board—little ball bearings” that prevent paint from latching directly to the base metal. Mechanical sanding temporarily cuts through it, but the film regenerates almost instantly. 4. **Self-Etching Primer:** The standard solution is an acid-etching primer containing phosphoric acid. The acid eats through the aluminum oxide, stripping it away while simultaneously depositing a stable, less reactive metallic barrier layer (such as zinc or iron phosphate) to ensure a bulletproof adhesive bond.
The presenter notes a specialized workshop alternative: spreading liquid epoxy directly onto the degreased aluminum and wet-sanding it straight into the bare substrate with an abrasive Scotch-Brite pad or sandpaper. Because the wet epoxy shields the freshly abraded surface from air, oxidation cannot occur, yielding the absolute highest bond strength possible. However, because this technique is messy, it is best reserved for small brackets or one-off parts rather than large sheets.
[36:24](https://www.youtube.com/watch?v=dNs_kNilSjk&t=2184s) Spraying Ultra-Thin HVLP Coats
The primed aluminum panel is set up for paint application using an HVLP (high-volume low-pressure) spray gun. The host bypasses basic gun tuning, pointing out that ample setup guides already exist online, but emphasizes the single most crucial painting discipline: applying extremely thin, multiple passes rather than heavy wet coats.
As the compressor runs and the first whisper-thin coat is laid down across the panel, the host stresses that laying on ultra-thin layers actually saves substantial time over the entire duration of the project by enabling rapid flash-off and preventing entrapment of evaporating solvent.
[37:13](https://www.youtube.com/watch?v=dNs_kNilSjk&t=2233s) Evaluating Dryness Between Coats and Interlaminar Bonding
Applying thin layers rather than heavy coats ensures maximum surface area for solvent evaporation, prevents unsightly runs, and avoids excessive waiting between layers. To gauge when a coat is ready for the subsequent application, the host relies on sensory cues rather than a rigid timer. First, the solvent sheen must vanish: wet paint looks glossy and reflective, but as the solvent flashes off, the finish turns completely flat and matte. Second, touching an inconspicuous area with a gloved finger should yield no transfer whatsoever. Third, a quick sniff test should confirm that a faint trace of solvent odor remains. Timing this sweet spot is critical for coating longevity. Reapplying prematurely traps solvent, allowing vapor pressure to push up blisters and bubbles under subsequent coats. Conversely, allowing the surface to turn bone-dry prevents the new solvent from chemically biting into and melting the underlying acrylic, destroying the interlaminar adhesion required to prevent delamination.
```mermaid flowchart TD accTitle: Recoat Window Evaluation Logic accDescr: Three-step sensory check determining whether paint is ready for another layer or outside the optimal recoat window. subgraph Checks["Sensory Evaluation"] A["Visual: Gloss disappears to flat matte"] --> B["Touch: Gloved finger comes away clean"] B --> C["Sniff: Faint trace of solvent odor remains"] end subgraph Decisions["Application Timing"] C -->|"Optimal timing"| D["Apply next coat: Solvent bites into acrylic for interlaminar bond"] C -->|"Too early (wet)"| E["Risk: Trapped solvent vapor blisters & bubbles"] C -->|"Too late (bone dry)"| F["Risk: Poor interlaminar adhesion, peeling & cracking"] end ```
After roughly 20 minutes of drying, the test panel displays an ultra-matte surface, passes the clean glove wipe, and still gives off a faint whiff of solvent. Addressing the matte appearance, the host dispels a common misconception regarding paint sheen and reflectivity, noting that surface texture does not dictate total solar reflectance. As he explains: “The gloss paint produces a specular reflection you can almost see your face in it but the matte paint will scatter the light nevertheless they both reflect the same percentage it's kind of a surprising fact and this is a very matte surface.” With the criteria satisfied, the loud compressor fires back up to deposit the second coat.
- Trapped solvent produces blisters and pinhole bubbling as rising vapor pressure attempts to escape through freshly laid acrylic coats. - Complete desiccation between passes prevents the incoming solvent from chemically etching the preceding layer, drastically elevating the risk of eventual cracking or peeling. - Specular reflection (mirror-like bounce from glossy finishes) and diffuse reflection (scattered bounce from matte finishes) can reflect the identical total fraction of incoming solar radiation.
---
[40:02](https://www.youtube.com/watch?v=dNs_kNilSjk&t=2402s) Speeding Up Dry Times and Managing Long Spray Sessions
Faced with dozens of coats ahead, the host opts to expedite the drying intervals by introducing an electric fan, though he warns viewers about the hazards of doing so outside an industrial spray booth. A fan creates turbulent air currents that can lift settled floor sweepings and blow dust directly onto the tacky panel. Furthermore, pointing high-velocity air at close range causes differential drying across the panel, leaving uneven moisture zones. To mitigate these threats, the fan is positioned far back, elevated well off the ground, and set to run exclusively on its lowest speed to deliver a gentle, non-focused draft.
Even with the process moving along, building up the required thickness is an endurance test. Each application pass lasts only one to two minutes, followed by a twenty-minute lull. With 95 percent of the day spent waiting around, the host suggests pairing paint days with secondary workshop projects or enlisting a partner to swap shifts, joking: “I'll do the first two hours and then my cameraman will do the last eight hours you know just to be fair.” The session continues through sustained snack breaks, banter over tools and production budgets, and repetitive spraying intervals that stretch deep into the evening. By the time the final layer is laid down, reference to a handwritten notepad confirms that approximately 27 consecutive coats have been applied to build the requisite barrier.
- Forced air increases particulate contamination risks on wet paint films unless the fan is elevated, placed at a distance, and operated at low speed. - The duty cycle of the painting process involves 1–2 minutes of spraying contrasted against 20-minute passive flash-off intervals. - The completed test workpiece accumulated roughly 27 individual sprayed coats before reaching the target film thickness.
---
[44:29](https://www.youtube.com/watch?v=dNs_kNilSjk&t=2669s) Outdoor Temperature Testing: Setup and Live Comparison
Following an overnight cure, a night of sleep, and several cups of coffee, the testing phase moves outdoors into the sunlight to evaluate whether the formulation can achieve genuine daytime radiative cooling. Three experimental panels of equal dimensions are arranged side by side under full sun: 1. An aluminum panel coated with the custom high-solids radiative cooling paint (~27 coats). 2. A bare, untreated aluminum plate. 3. An aluminum panel coated with commercial Rust-Oleum high-brightness white paint.
To gather precise comparative data, individual contact thermal probes are affixed to the backside of each panel and wired into a multi-channel digital thermocouple thermometer: channel 1 monitors the ultra paint panel, channel 2 tracks the bare aluminum panel, and channel 3 monitors the commercial Rust-Oleum panel. A fourth standalone probe hangs freely in the shade behind the test backer to establish the real-time ambient air temperature benchmark. The array is powered on and left to equilibrate in the autumn sunlight before logging final thermal performance metrics.
---
[46:47](https://www.youtube.com/watch?v=dNs_kNilSjk&t=2807s) Test Results: Sub-Ambient Cooling and Real-World Implications
Once thermal equilibrium is established, the digital thermometer reveals a striking divergence in performance across the three samples. The panel coated in the custom radiative cooling paint measures approximately 3 °C colder than the ambient outdoor air temperature. In stark contrast, the bare aluminum plate absorbs significant energy and runs roughly 20 °C hotter than ambient air, while the panel coated in standard Rust-Oleum super white sits 8 °C to 10 °C above ambient.
| Surface / Panel Sample | Thermal Performance Relative to Ambient Air | |:--- |:--- | | **Custom Radiative Ultra Paint** | **~3 °C below ambient (sub-ambient cooling)** | | **Rust-Oleum Commercial Super White** | ~8 °C to 10 °C above ambient | | **Bare Aluminum Plate** | ~20 °C above ambient |
The host emphasizes that this test takes place under exceptionally conservative real-world conditions. Conducted during a New England afternoon in November, solar intensity is considerably lower than peak summer values, which compresses the performance spreads that would otherwise widen significantly under high-intensity summer sun or at equatorial latitudes. Furthermore, the test setup lacks parasitic thermal shielding: the panels are fully exposed to ambient infrared radiation radiating off surrounding trees, nearby buildings, and the camera crew, while convective wind actively tries to heat the sub-ambient panel up to air temperature while cooling the hotter panels down. As the host underscores: “Meaning if you were to put this on an actual structure or a building or the roof of your house in Tunisia you would have those surfaces cooler than the surrounding air given realworld conditions pretty impressive.”
Wrapping up the demonstration, the host notes that while building the paint requires careful formulation, high-purity pigments, and diligent application, the ability to achieve sub-ambient passive refrigeration on standard architectural building materials represents a transformative technology. He concludes by thanking viewers and encouraging channel subscriptions to fund ongoing experimental hardware builds.
- Testing conditions: New England autumn (November afternoon), unshielded from ambient terrestrial infrared or convective wind warming. - Despite convective air currents constantly working to add heat back into sub-ambient objects, the ultra-paint panel maintained a continuous 3 °C depression below ambient air.
## Mentioned Tech Ingredients, Barium sulfate, EDTA, Polymethyl methacrylate (PMMA), Dimethylformamide (DMF), NighthawkInLight, KitchenAid, Airtech Pvt. Ltd., US Nano, Lucite International, Mitsubishi Chemical, PolySciences, Elvacite 2028, Zahn cup, Ford/Wagner cup, Rust-Oleum
## Video description This a follow-up to our most recent video https://youtu.be/5zW9_ztTiw8 where we show you our custom built liquid panel that when placed outside, cools down to lower than ambient temperature. Today's video shows you how to create and use the specialty paint that makes the panel possible.
Find us on Patreon and our website: https://www.patreon.com/techingredients https://www.techingredients.com/
[Source](https://www.youtube.com/watch?v=dNs_kNilSjk)