Glass powders are widely used in fabricating sintered glasses, sintered glassÀceramics, glass matrix composites, seals, and glass-bonded ceramics or pastes. [1][2][3] For many of these applications, glasses with low crystallization tendency are used, for example, for low-temperature cofired ceramics, [4,5] pastes, [6] or sealants [7,8] to ensure sufficient sinterability.Due to the low viscosity required for joining and gas tight sealing, gas bubble formation and subsequent swelling (foaming) often occur, even when organic aids are not used in powder processing. In contrast to the extensive and ongoing study of desired foaming phenomena utilized for foam glasses or glassÀceramic foams, [9][10][11][12][13][14][15] this nondesired foaming effect and its underlying mechanisms are rarely reported. Lucchini [16] observed bubble formation for sodium and calcium lead silicate glass-bonded barium hexaferrites and discussed glass volatilization as the underlying mechanism. Pore formation was also found in porcelain stoneware tiles [17] and lead borosilicate glass frits, [18] where effusing oxygen or water, physically or chemically adsorbed to the powder surface, was discussed as the foaming source. Lara et al. [19] reported foaming during the sintering and crystallization of Ca, Mg, and Zn alumosilicate glass powders used for solid oxide fuel cell (SOFC) sealing. The authors believed that density changes or gas evolution during crystallization are responsible for foaming. Undesired porosity was also reported to occur during sintering of BaO-B 2 O 3 -SiO 2 , [20] lead-free Bi 2 O 3 -B 2 O 3 -SiO 2 solder glass, [21] LTCC glass powders; [22] as well as during porcelain tiles production. [23] More recently, Agea-Blanco et al. [24] studied sintering and foaming of commercial barium zinc alumino boro silicate glass powders, used for SOFC sealing, with heating microscopy, differential thermal analysis (DTA), and vacuum hot extraction (VHE). It was shown that foaming intensity increases with milling duration. For moderately milled glass powders, consecutive storage in air could also promote foaming. Although powder compacts were pressed and sintered in air, foaming was affected by different milling atmospheres among which CO 2 proved to enhance foaming most strongly. Similarly, VHE studies revealed that foaming is predominantly driven by C, CO, and CO 2 , even for powders milled in Ar and N 2 . It was therefore concluded that foaming is caused by carbonaceous species adsorbed on the glass powder surface during milling and later storage.The present study is focused on the nature of these species and the mechanisms keeping them trapped during heating to the temperature of foaming. To ensure detectable amounts of foaming species, K01 glass powders were milled for several hours. Recrushed powder compacts, or those heated to different temperatures and quenched in air were studied with heating