Every year the problem of water purification becomes more relevant. This is due to the continuous increase in the level of pollution of natural water sources, an increase in the population, and sharp climatic changes. The growth in demand for affordable and clean water is not always comparable to the supply that exists in the water treatment market. In addition, the amount of water pollution increases with the increase in production capacity, the purification of which cannot be fully handled by conventional processes. However, the application of novel nanomaterials will enhance the characteristics of water treatment processes which are one of the most important technological problems. In this review, we considered the application of carbon nanomaterials in membrane water purification. Carbon nanofibers, carbon nanotubes, graphite, graphene oxide, and activated carbon were analyzed as promising materials for membranes. The problems associated with the application of carbon nanomaterials in membrane processes and ways to solve them were discussed. Their efficiency, properties, and characteristics as a modifier for membranes were analyzed. The potential directions, opportunities and challenges for application of various carbon nanomaterials were suggested.

Room-temperature gas sensors based on granulated carbon nanofiber material were investigated for the detection of NO₂. The granulated material consisting of intertwined carbon nanofibers was synthesized by the decomposition of CH₄ over the Ni/Al₂O₃ catalyst in a vibro-fluidized bed reactor. Carbon material was investigated using transmission electron microscopy, Raman spectroscopy, low-temperature nitrogen adsorption, and X-ray photoelectron spectroscopy. Investigation of the gas sensors towards NO₂ at room temperature (25 ± 2 °C) was carried out in a dynamic flow-through setup in the range from 1 to 500 ppm. A comparison of the sensitivity gas sensor to NH₃ and CH₄ was also given. The sensor based on non-treated carbon nanofiber material showed the response ΔR/R₀ of 5.1 % to 10 ppm of NO₂. It was found that the sensor response to NO₂ decreased when increasing the relative humidity. The effect of the relative humidity was more pronounced for low concentrations of nitrogen dioxide and decreases with a further increase in them.

Highly porous expanded graphite was synthesized by the programmable heating technique using heating with a constant rate (20 °C/min) from room temperature to 400–700 °C. The samples obtained were analyzed by scanning electron microscopy, energy-dispersive spectroscopy, low-temperature nitrogen adsorption, X-ray photoelectron spectroscopy, Raman spectroscopy, thermogravimetry, and differential scanning calorimetry. A comparison between programmable heating and thermal shock as methods of producing expanded graphite showed efficiency of the first one at a temperature 400 °C, and the surface area reached 699 and 184 m²/g, respectively. The proposed technique made it possible to obtain a relatively higher yield of expanded graphite (78–90%) from intercalated graphite. The experiments showed the advantages of programmable heating in terms of its flexibility and the possibility to manage the textural properties, yield, disorder degree, and bulk density of expanded graphite.

In this paper, room-temperature chemiresistive gas sensors for NO₂ detection based on CVD-grown carbon nanofibers (CNFs) were investigated. Transmission electron microscopy, low-temperature nitrogen adsorption, and X-ray diffraction were used to investigate the carbon nanomaterials. CNFs were synthesized in a wide range of pressure (1–5 bar) by CO_x-free decomposition of methane over the Ni/Al₂O₃ catalyst. It was found that the increase in pressure during the synthesis of CNFs induced the later deactivation of the catalyst, and the yield of CNFs decreased when increasing pressure. Sensing properties were determined in a dynamic flow-through installation at NO₂ concentrations ranging from 1 to 400 ppm. Ammonia detection was tested for comparison in a range of 100–500 ppm. The obtained sensors based on CNFs synthesized at 1 bar showed high responses of 1.7%, 5.0%, and 10.0% to 1 ppm, 5 ppm, and 10 ppm NO₂ at 25 ± 2 °C, respectively. It was shown that the obtained non-modified carbon nanomaterials can be used successfully used for room temperature detection of nitrogen dioxide. It was found that the increase in relative humidity (RH) of air induced growth of response, and this effect was facilitated after reaching RH ~35% for CNFs synthesized at elevated pressures.

This article is devoted to the investigation of the sensing behavior of chemically treated multi-walled carbon nanotubes (MWNTs) at room temperature. Chemical treatment of MWNTs was carried out with a solution of either sulfuric or chromic acids. The materials obtained were investigated by transmission electron microscopy, scanning electron microscopy, Raman-spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. The active layer of chemiresistive gas sensors was obtained by cold pressing (compaction) at 11 MPa of powders of bare and treated multi-walled carbon nanotubes. The sensing properties of pellets were investigated using a custom dynamic type of station at room temperature (25 ± 2 °C). Detection of NO₂ was performed in synthetic air (79 vol% N₂, 21 vol% O₂). It was found that the chemical treatment significantly affects the sensing properties of multi-walled carbon nanotubes, which is indicated by increasing the response of the sensors toward 100–500 ppm NO₂ and lower concentrations.

Graphite oxides obtained by a modified Hummers method were studied using scanning electron microscopy, X-ray diffraction, energy dispersive X-ray spectrosc