Special Issue on “Syntheses and Industrial Use of Monodispersed Colloidal Particles”

AbstractThe motivation for this special issue on circular economy, and national and global policy, originated during the international stakeholder meeting (Ochoa 2019) for our SUNRISE flagship project (Abbott 2019; Kupferschmidt 2019) in Bruxelles in June 2019. At the same day, one mile away from our meeting, Deutsche Energie Agentur (DENA) held a panel round table meeting on regulation for renewable fuels (Powerfuels 2019), at which the author could participate. The SUNRISE flagship is a European initiative for the sustainable production of solar fuels and base chemicals. The yet to be developed technology is based on the chemical reduction of carbon dioxide (CO2) from concentrated sources and from the atmosphere, and solar water splitting for hydrogen production. Hydrogen and carbon dioxide will be synthesized to hydrocarbons for industrial use. When the synthetic hydrocarbons are consumed, carbon dioxide will be generated and fed back in a circular process, powered by renewable energy. In this extended carbon cycle (Calvin 1961), CO2 is a valuable asset and remains part of the global biogeochemical cycle and becomes part of the circular economy. CO2 concentration in the atmosphere will be reduced to an acceptable, climate neutral value once the cycle is in operation (Faber et al. 2020).

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Ultrastructure of Lymphatic Capillaries in the Transport of Colloidal Particles

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100060945 ◽

1967 ◽

Vol 25 ◽

pp. 186-187

Author(s):

L. V. Leak ◽

J. F. Burke

Keyword(s):

Connective Tissue ◽

Colloidal Particles ◽

Ultrastructural Level ◽

Vital Role ◽

Time Intervals ◽

Thorium Dioxide ◽

Lymphatic Capillary ◽

Tissue Area ◽

Rapid Removal ◽

Tissue Fluids

The vital role played by the lymphatic capillaries in the transfer of tissue fluids and particulate materials from the connective tissue area can be demonstrated by the rapid removal of injected vital dyes into the tissue areas. In order to ascertain the mechanisms involved in the transfer of substances from the connective tissue area at the ultrastructural level, we have injected colloidal particles of varying sizes which range from 80 A up to 900-mμ. These colloidal particles (colloidal ferritin 80-100A, thorium dioxide 100-200 A, biological carbon 200-300 and latex spheres 900-mμ) are injected directly into the interstitial spaces of the connective tissue with glass micro-needles mounted in a modified Chambers micromanipulator. The progress of the particles from the interstitial space into the lymphatic capillary lumen is followed by observing tissues from animals (skin of the guinea pig ear) that were injected at various time intervals ranging from 5 minutes up to 6 months.

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Deposited emulsion particles in the pores of aluminum oxide film

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100109392 ◽

1978 ◽

Vol 36 (1) ◽

pp. 450-451

Author(s):

Michio Ashida ◽

Yasukiyo Ueda

Keyword(s):

Oxide Film ◽

Acid Solution ◽

Barrier Layer ◽

Colloidal Particles ◽

Oxalic Acid Solution ◽

Anodic Oxide ◽

Anodic Oxide Film ◽

Carbon Replica ◽

Sectioning Method ◽

Thin Sectioning

An anodic oxide film is formed on aluminum in an acidic elecrolyte during anodizing. The structure of the oxide film was observed directly by carbon replica method(l) and ultra-thin sectioning method(2). The oxide film consists of barrier layer and porous layer constructed with fine hexagonal cellular structure. The diameter of micro pores and the thickness of barrier layer depend on the applying voltage and electrolyte. Because the dimension of the pore corresponds to that of colloidal particles, many metals deposit in the pores. When the oxide film is treated as anode in emulsion of polyelectrolyte, the emulsion particles migrate onto the film and deposit on it. We investigated the behavior of the emulsion particles during electrodeposition.Aluminum foils (99.3%) were anodized in either 0.25M oxalic acid solution at 30°C or 3M sulfuric acid solution at 20°C. After washing with distilled water, the oxide films used as anode were coated with emulsion particles by applying voltage of 200V and then they were cured at 190°C for 30 minutes.

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Ultrastructure of mesotheliomas

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100110775 ◽

1984 ◽

Vol 42 ◽

pp. 98-101

Author(s):

Irving Dardick

Keyword(s):

Electron Microscopy ◽

Latent Period ◽

Spindle Cell ◽

Spindle Cell Sarcoma ◽

Metastatic Adenocarcinoma ◽

Cell Sarcoma ◽

Cytological Features ◽

Industrial Use ◽

Degree Of Differentiation

With the extensive industrial use of asbestos in this century and the long latent period (20-50 years) between exposure and tumor presentation, the incidence of malignant mesothelioma is now increasing. Thus, surgical pathologists are more frequently faced with the dilemma of differentiating mesothelioma from metastatic adenocarcinoma and spindle-cell sarcoma involving serosal surfaces. Electron microscopy is amodality useful in clarifying this problem.In utilizing ultrastructural features in the diagnosis of mesothelioma, it is essential to appreciate that the classification of this tumor reflects a variety of morphologic forms of differing biologic behavior (Table 1). Furthermore, with the variable histology and degree of differentiation in mesotheliomas it might be expected that the ultrastructure of such tumors also reflects a range of cytological features. Such is the case.

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