Abstract. We present the laboratory results of immersion freezing efficiencies of cellulose particles at supercooled temperature (T) conditions. Three types of chemically homogeneous cellulose samples are used as surrogates that represent supermicron and submicron ice-nucleating plant structural polymers. These samples include microcrystalline cellulose (MCC), fibrous cellulose (FC) and nanocrystalline cellulose (NCC). Our immersion freezing dataset includes data from various ice nucleation measurement techniques available at 17 different institutions, including nine dry dispersion and 11 aqueous suspension techniques. With a total of 20 methods, we performed systematic accuracy and precision analysis of measurements from all 20 measurement techniques by evaluating T-binned (1 ∘C) data over a wide T range (−36 ∘C <T<-4 ∘C). Specifically, we intercompared the geometric surface area-based ice nucleation active surface site (INAS) density data derived from our measurements as a function of T, ns,geo(T). Additionally, we also compared the ns,geo(T) values and the freezing spectral slope parameter (Δlog(ns,geo)/ΔT) from our measurements to previous literature results. Results show all three cellulose materials are reasonably ice active. The freezing efficiencies of NCC samples agree reasonably well, whereas the diversity for the other two samples spans ≈ 10 ∘C. Despite given uncertainties within each instrument technique, the overall trend of the ns,geo(T) spectrum traced by the T-binned average of measurements suggests that predominantly supermicron-sized cellulose particles (MCC and FC) generally act as more efficient ice-nucleating particles (INPs) than NCC with about 1 order of magnitude higher ns,geo(T).

Phenolic compounds are common constituents of atmospheric aerosols. They form by pyrolysis of lignin and by biodegradation of plant material and are commonly found in biomass burning plumes, resuspended soil dust, and in anthropogenic secondary organic aerosols (SOA). In this study, we show that reactions of Fe­(III), a major constituent of mineral dust, with several phenolic compounds (guaiacol, catechol, syringol, o- and p-cresol) that are common in atmospheric aerosols, result in the formation of water insoluble light-absorbing compounds and reduced Fe­(II). The study was conducted under acidic conditions (pH = 1–2), relevant for areas impacted by biomass burning, anthropogenic emissions, and mineral dust. The reaction products have been characterized using a high-performance liquid chromatography coupled to photodiode array and high-resolution mass spectrometry detectors, UV–visible spectroscopy, X-ray photoelectron spectroscopy, and thermal gravimetric analysis. The major identified chromophores are oligomers of the reaction precursors that efficiently absorb light between 300 and 500 nm. The amounts of oligomers vary significantly between the systems studied. The highest amount was observed for guaiacol and catechol, and the least were detected in the syringol experiments, suggesting that the oligomerization proceeds through carbon–carbon coupling preferred at para- and ortho- positions, coupled to the reduction of Fe­(III) to Fe­(II). The results suggest that aqueous-phase radical reactions of phenolic compounds may be an efficient source of light-absorbing atmospheric organic compounds (brown carbon) that play important roles in Earth’s radiative forcing on global and regional scales and of quinones that can affect health.

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