Phase equilibria of fluid mixtures are important in numerous industrial applications and are, thus, a major focus of thermophysical property research. Improved data, particularly along the dew line, are needed to improve model predictions. Here we present experimental results utilizing highly accurate densimetry to quantify the effects of sorption and capillary condensation, which exert a distorting influence on measured properties near the dew line. We investigate the (pressure, density, temperature, composition) behaviour of binary (CH 4 + C 3 H 8 ) and (Ar + CO 2 ) mixtures over the temperature range from (248.15 to 273.15) K starting at low pressures and increasing in pressure towards the dew point along isotherms. Three distinct regions are observed: (1) minor sorption effects in micropores at low pressures; (2) capillary condensation followed by wetting in macro-scale surface scratches beginning approximately 2% below the dew-point pressure; (3) bulk condensation. We hypothesize that the true dew point lies within the second region.Fluid mixtures are important in many scientific and industrial applications. In this context, accurate knowledge about phase equilibria and in particular about the dew line, which separates the homogeneous vapour region from the heterogeneous two-phase (vapour-liquid) region, is essential. The investigation of the phase behaviour of fluid mixtures is a major focus of thermophysical property research for both a fundamental understanding of the behaviour of fluid mixtures and for practical applications including natural gas processing and carbon capture and storage (CCS). For example, equipment in gas pipelines must be protected from damage due to the condensation of the fluid being handled. Therefore, accurate property models are required for the design and operation of industrial processes. Such models are based on accurate experimental data, but there are significant gaps and deficiencies in the existing data sets, which impede the required improvement of mixture models.Thermophysical property measurements in the vicinity of the dew line of fluid mixtures can be substantially distorted by sorption and condensation effects. This is due to the preferential sorption or condensation of one or more component(s), which changes the vapour composition from that originally loaded into the measuring cell of an experimental apparatus. (The condensed material is enriched in the least volatile component(s), although this can vary with adsorption due to other factors). The study of sorption phenomena is a very active and mature scientific field, with application to gas purification and gas separation, among many other application areas. However, sorption is usually studied on porous media (i.e., materials with a large surface area on the microscale) such as activated carbon, zeolites or metal-organic frameworks, but not on the simple metal surfaces (which are often highly polished) existing in property measurement instruments.It has long been recognized that sorption effects and, in particul...