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Concrete production accounts for 7%–8% of global carbon emissions, with cement calcination as the primary source of emissions. As the world’s largest cement producer, China’s cement industry contributes roughly 13% of domestic carbon output, making low-carbon concrete development a core strategy to hit carbon peaking and carbon neutrality goals.
A mainstream low-carbon solution is replacing large portions of cement with industrial solid waste mineral admixtures, including blast furnace slag, fly ash, and ground calcium carbonate. Replacement rates commonly reach 30%–50%, drastically reducing clinker consumption and CO₂ output. Polycarboxylate superplasticizers (PCE) are irreplaceable admixtures for modern concrete, relying on electrostatic repulsion and steric hindrance to disperse cement flocs and release trapped free water.
However, PCE superplasticizers exhibit selective adsorption on different mineral powder surfaces. Traditional PCE formulas exhibit inconsistent behavior in pure cement versus high-mineral blended binder systems. This article conducts a comprehensive lab comparison of two distinct PCE products across three binder groups: pure cement, 50% slag-blended, and composite fly ash-calcium carbonate-blended mixes. Evaluation metrics cover initial fluidity, flow loss over time, slurry viscosity, and low-temperature adaptability, delivering technical guidance for custom low-carbon concrete PCE admixtures.
Cement: P.I 42.5 pure Portland cement, compliant with GB 8076-2008 admixture testing standards (marked C).
Mineral admixtures:
Two PCE superplasticizers (water reduction rate >30%):
| Group Code | Portland Cement | Slag (SL) | Fly Ash (FA) | Calcium Carbonate (CC) |
| C100 | 100% | 0% | 0% | 0% |
| C50SL50 | 50% | 50% | 0% | 0% |
| C50FA25CC25 | 50% | 0% | 25% | 25% |
| Fixed water-binder ratio = 0.30 for all slurry tests. |
Low temperature slows PCE adsorption kinetics and exacerbates early flow loss. Overall, high mineral blended binders deliver better PCE temperature tolerance than pure cement systems:
1. Pure cement C100
PCE1: Initial flow drops sharply at 5 °C due to slowed polymer adsorption on cement grains.
PCE2: Minor initial flow improvement under cold conditions, low temperature sensitivity.
All pure cement slurries lose flow within the first 10 min at low temperature, followed by mild rebound, weaker than at room temperature.
2. C50SL50 50% slag system
Trend mirrors pure cement, yet the rebound magnitude is suppressed by a lower overall PCE dosage.
3. C50FA25CC25 fly ash-carbonate system
Both PCE types gain slight initial flow at 5 °C, but PCE2 suffers more severe early flow loss over time.
Temperature sensitivity directly correlates with molecular side-chain length and the differences in adsorption rate between the two PCE chemistries.
Mass replacement of cement with industrial mineral waste is the primary pathway to produce low-carbon concrete and cut construction carbon footprints. The two mainstream polycarboxylate ether superplasticizers, PCE1 and PCE2, exhibit markedly different flow, viscosity and temperature performance across pure cement versus high-mineral binder groups, driven by selective polymer adsorption on distinct mineral surfaces.
Construction material engineers and admixture manufacturers can match the correct PCE formula according to binder composition (slag-only or fly ash-carbonate composite blends). Optimized PCE selection minimizes admixture cost, stabilizes slurry workability during transport, and delivers reliable performance under both normal and low-temperature construction conditions, supporting the widespread adoption of sustainable, low-carbon concrete worldwide.

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