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You are here: BAILII >> Databases >> United Kingdom Upper Tribunal (Tax and Chancery Chamber) >> Singleton Birch Ltd & Anor v Revenue and Customs (LANDFILL TAX - section 42(2) Finance Act 1996 - Landfill Tax (Qualifying Material) Order 2011 - Note 9(a) - whether waste was entirely "calcium based reaction waste from titanium dioxide production" - whether FTT applied the right test) [2025] UKUT 72 (TCC) (28 February 2025) URL: http://www.bailii.org/uk/cases/UKUT/TCC/2025/72.html Cite as: [2025] UKUT 72 (TCC) |
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Tax and Chancery Chamber
Fetter Lane London EC4A 1NL |
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Judgment Date: 28 February 2025 |
B e f o r e :
JUDGE ANNE REDSTON
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(1) SINGLETON BIRCH LIMITED (2) FCC RECYCLING (UK) LIMITED |
Appellant |
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- and - |
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THE COMMISSIONERS FOR HIS MAJESTY'S REVENUE AND CUSTOMS |
Respondents |
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For the Appellants: Akash Nawbatt KC and Colm Kelly of counsel, instructed by Stewarts Law LLP
For the Respondents: James Puzey and Joseph Millington of counsel, instructed by the General Counsel and Solicitor for His Majesty's Revenue and Customs
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Crown Copyright ©
LANDFILL TAX section 42(2) Finance Act 1996 Landfill Tax (Qualifying Material) Order 2011 Note 9(a) whether waste was entirely "calcium based reaction waste from titanium dioxide production" whether FTT applied the right test no decision set aside and re-made appeal against the original assessment dismissed
Introduction
calcium based reaction wastes from titanium dioxide production;
The FTT's findings of fact
Relevant legislation
42 Amount of tax
(1) The amount of tax charged on a taxable disposal shall be found by taking
(a) £84.40 for each whole tonne disposed of and a proportionately reduced sum for any additional part of a tonne, or
(b) a proportionately reduced sum if less than a tonne is disposed of.
(2) Where the material disposed of consists entirely of qualifying material or qualifying fines this section applies as if the reference to £84.40 were to £2.65.
(3) Qualifying material is material for the time being listed for the purposes of this section in an order.
(4) The Treasury must
(a) set criteria to be considered in determining from time to time what material is to be listed or what fines are to be qualifying fines,
(b) keep those criteria under review, and
(c) revise them whenever they consider they should be revised.
(5) The Commissioners must publish the criteria (and any revised criteria) set by the Treasury.
(6) In determining from time to time what material is to be listed, or what fines are to
be qualifying fines, the Treasury must have regard to
(a) the criteria (or revised criteria) published under subsection (5), and
(b) any other factors they consider relevant.
63 Qualifying material: special provisions
(1) This section applies for the purposes of section 42 above.
(2) The Commissioners may direct that where material is disposed of it must be treated as qualifying material if it would in fact be such material but for a small quantity of non-qualifying material; and whether a quantity of non-qualifying material is small must be determined in accordance with the terms of the direction.
(3) The Commissioners may at the request of a person direct that where there is a disposal in respect of which he is liable to pay tax the material disposed of must be treated as qualifying material if it would in fact be such material but for a small quantity of non-qualifying material
3. Subject to articles 4 to 6, the material listed in column 2 of the Schedule to this Order ("the
Schedule") is qualifying material for the purpose of section 42 of the Finance Act 1996.
4. The Schedule shall be construed in accordance with the notes contained in it.
Column 1 | Column 2 | Column 3 |
Group | Description of material | Conditions |
6 | Low activity inorganic compounds |
Notes
(9) Group 6 comprises only
(a) calcium based reaction wastes from titanium dioxide production;
(b) calcium carbonate;
(c) magnesium carbonate;
(d) magnesium oxide;
(e) magnesium hydroxide;
(f) iron oxide;
(g) ferric hydroxide;
(h) aluminium oxide;
(i) aluminium hydroxide;
(j) zirconium dioxide.
Context of the relevant legislation
(1) material describing the environmental objectives underpinning the relevant statutory provisions;
(2) the consultation which preceded enactment of the QMO;
(3) the Treasury criteria by reference to which waste materials are included in the QMO; and
(4) material describing the environmental policy context.
Environmental objectives
(a) prevention;
(b) preparing for re-use;
(c) recycling;
(d) other recovery (for example energy recovery);
(e) disposal.
Consultation preceding the QMO
(1) landfill tax is intended to reflect the environmental impact associated with the actual landfilling of waste;
(2) where waste serves as a substitute for virgin material for engineering purposes at a landfill site, that waste should not be taxed;
(3) the rationale for the lower rate of tax is the relatively low level of environmental impact associated with landfilling inert wastes;
(4) landfill tax should provide an incentive to find more sustainable uses and treatments for waste.
The residue from titanium dioxide manufacture will qualify, rather than titanium dioxide itself, reflecting industry views.
Environmental policy
The FTT decision
71. As for the application of the legislation, when construed as described above, in the light of the evidence, it was common ground that:
(1) the language of Section 42(2) of the FA 1996 and Note (9)(a) did not require that, in order to qualify for the lower rate, a waste needed to be composed entirely of calcium reacted compounds;
(2) the language was not focused on the elements which were the components of the waste but rather on the reactions which had led to the waste; and
(3) the reactions giving rise to the creation of the FCC waste were primarily between calcium compounds within the APCRs and the [ferrous chloride].
72. However, there was a disagreement between the parties in relation to the extent to which waste needed to be the product of a reaction between calcium compounds and the [ferrous chloride] in order to satisfy the statutory language.
116. we have reached the conclusion that the FCC waste does not consist entirely of calcium based reaction waste from titanium dioxide production. Indeed, we think that that conclusion is self-evident, essentially for the reasons given by Mr Puzey and summarised in paragraphs 71 to 89 above.
(1) The FCC Waste was as much, if not more, a product of neutralising the APCR with the ferrous chloride as it was the other way around. The FTT noted the presence of substantial non-reactive material in the APCR and the amount of APCR required to neutralise one tonne of ferrous chloride. Hence, the mere fact that the reactions creating the FCC Waste were primarily with calcium compounds in the APCR did not mean that the resulting waste was entirely a calcium based reaction waste from titanium dioxide production: see [74] and [86].
(2) Between 70% and 90% of the APCR was non-reactive and not all of the reactive compounds in the APCR were calcium based. For example, 11.4% of one sample of APCR consisted of potassium compounds, which were potentially reactive: see [76].
(3) Some 3.9 tonnes of APCR were required to neutralise 1 tonne of ferrous chloride: see [77].
(4) Between 57% and 72% of the FCC Waste did not result from a reaction between alkaline compounds in the APCR and the acidic ferrous chloride. That was before taking into account that not all the alkaline compounds in the APCR were calcium compounds: see [80].
(5) The APCR used to create the FCC Waste could not be compared to the slaked lime slurry used to create the Cristal Waste. 99.4% of the slaked lime which was used to create the slurry was pure calcium hydroxide. This was very different to the impurities and non-calcium compounds in the APCR. Further, the water used to make the slurry was an essential part of the process because the calcium hydroxide had to be diluted for the calcium based chemical reaction to occur: see [83].
(6) The fact that a lower rate for the FCC Waste would be consistent with the principles and aims of the environmental legislation, the waste hierarchy, best available techniques, the consultation process and the Treasury criteria could not override the plain meaning of the statutory provisions. The FCC Waste did not consist entirely of calcium based reaction waste from titanium dioxide production: see [88] and [89].
121. However, none of the above matters can override the clear language which is used in Section 42(2) of the FA 1996 and the QMO. They can provide some context but they are not a substitute for examining the language actually used and, when one turns to considering whether the FCC waste can be said to "consist entirely of calcium based reaction waste from titanium dioxide production", we think that it is self-evident that it does not. As Mr Puzey succinctly pointed out, more than half of the FCC waste was neither reaction waste nor derived from titanium dioxide production. It is therefore clear that the FCC waste does not consist entirely of calcium-based reaction waste from titanium dioxide production.
122. We agree with Mr Puzey that:
(1) the relatively low level of reactive material within the APCRs;
(2) the presence of non-calcium based reactive materials within the APCRs; and
(3) the amount of APCRs required to neutralise the [ferrous chloride],
mean that, although the process at FCC Knostrop undoubtedly included a reaction between the calcium hydroxide (and certain other calcium based reactive compounds) within the APCRs and the [ferrous chloride], somewhere between 57% and 72% of the FCC waste consisted of material which was not the result of a calcium based reaction at all. To a very significant extent, the FCC waste simply consisted of elements which were part of the APCRs and which did not react with the [ferrous chloride].
123. We also agree with Mr Puzey that the process which took place at FCC Knostrop is more accurately described as the neutralisation of the APCRs using [ferrous chloride] than the neutralisation of the [ferrous chloride] using APCRs. The Second Appellant recognised this in:
(1) referring to the plant where the APCRs and the [ferrous chloride] were processed as the "Ash Plant";
(2) calling the log in which it recorded the process the "Ash Plant Log"; and
(3) including a column in that log headed "Treated Ash Quality".
As Mr Martin readily admitted at the hearing, the "Ash" referred to in each of those contexts was the APCRs and not the [ferrous chloride]. Thus, those references all support the conclusion that the process which was going on at FCC Knostrop is more properly described as the treatment of the APCRs with [ferrous chloride] than as the treatment of the [ferrous chloride] with APCRs and that the majority of the FCC waste was simply the treated APCRs waste and not the treated [ferrous chloride] waste derived from the production of titanium dioxide.
124. We should make it clear that we do not base our conclusion on the mere fact that the process at FCC Knostrop happened to involve the neutralisation of the APCRs at the same time as the [ferrous chloride] was neutralised. We recognise that that is no different from the fact that the process at Stallingborough involves the neutralisation of the virgin calcium hydroxide slurry at the same time as the [ferrous chloride] is neutralised. Instead, our conclusion is based on:
(1) the extent of the non-reactive material and the non-calcium based reactive material within the APCRs and the amount of the APCRs which were required for the process see paragraph 122 above; and
(2) our view, supported by the view of those conducting the process, that the essence of the process involved the neutralisation of the APCRs with [ferrous chloride] and not vice versa see paragraph 123 above.
125. For the reasons set out above, notwithstanding the principles of statutory construction which we were urged by Mr Nawbatt to apply, we cannot see how the FCC waste can properly be said to satisfy the statutory language. Quite simply, the FCC waste did not consist entirely of calcium based reaction waste from titanium dioxide production and the fact that the use of APCRs instead of slaked lime to neutralise the [ferrous chloride] may fit better with the UK environmental legislation, may be consistent with the process of consultation leading to the enactment of the QMO and may be consistent with the Treasury criteria is not sufficient to make it so.
129. In our view, the starting point in determining whether or not a particular waste product consists entirely of calcium based reaction waste from titanium dioxide production is not to ask whether all of that waste product is the result of a reaction between alkaline calcium compounds and the acid arising from titanium dioxide production. Instead, one should instead consider whether the essence of the process by which the relevant waste product has been produced involves a reaction between alkaline calcium compounds and the acid arising from titanium dioxide production. As long as the latter is the case, then the waste product resulting from the process in question consists entirely of calcium based reaction waste from titanium dioxide production. Moreover, that is the case regardless of whether:
(1) the alkaline solution which is used to neutralise the acid contains reactive elements other than calcium; or
(2) some of the end waste product is not the result of a reaction between a calcium compound in the alkaline solution and the acid.
130. Applying that test in the present case, it is plain that the essence of the process which takes place at Stallingborough is exactly as described in paragraph 129 above. In other words, the only purpose of the process is to neutralise the [ferrous chloride] that has arisen from titanium dioxide production. That remains the case despite the fact that:
(1) the virgin calcium hydroxide slurry which gives rise to the reaction contains a small amount of reactive elements other than calcium; and
(2) some of the constituent elements of the resulting Cristal waste are not the result of a reaction between a calcium compound and the FC.
131. The Cristal waste displays both of the features described in paragraphs 130(1) and 130(2) above because:
(1) there are some de minimis impurities in the slaked lime which is the basis of the virgin calcium hydroxide slurry that is applied to the [ferrous chloride]; and
(2) that slurry contains water, which could be tap water or water arising from the titanium dioxide production at Cristal's plant, and that water itself contains impurities.
132. However, the crucial point is that those impurities are simply unavoidable features of the calcium based reaction which is the essence of the process giving rise to the Cristal waste or, to put it another way, unavoidable features of the alkaline which is required to be applied in order to achieve the end objective of neutralising the [ferrous chloride] with calcium hydroxide. They do not change that end objective and thus they do not change the essence of the process which is occurring at the site. Instead, that essence remains the neutralisation of the [ferrous chloride] arising from titanium dioxide production by way of a reaction between a reactive alkaline which is calcium-based and that [ferrous chloride].
133. We say that because:
(1) the minimal impurities in the slaked lime are not there by design they are there simply because the slaked lime originates from the excavation of calcium carbonate from quarries and then the addition of water to the calcium oxide which results from heating that calcium carbonate to a very high temperature in a kiln. They are thus an inevitable feature of the steps which need to be taken to produce the slaked lime in the first place. The material which is excavated from the quarries inevitably contains traces of elements other than calcium carbonate and so too does the water which is added to convert the calcium oxide into calcium hydroxide; and
(2) the elements contained in the water which is used to create the slurry are there because the slaked lime is highly reactive and therefore needs to be diluted in order properly to carry out the calcium-based reaction.
The fact that those impurities are simply unavoidable features of the process leading to the end objective of neutralising the [ferrous chloride] arising from titanium dioxide production with a reactive alkaline solution that is largely calcium based and are not there for any other reason means they do not change the essence of the process, which is to do just that. Moreover, prior to its dilution in the water, at least 90%, and very likely a considerably greater percentage, of the slaked lime consists of pure calcium hydroxide. (We agree with Mr Puzey's observation that the 90% figure is likely to be a very conservative estimate as the supplier of the slaked lime, the First Appellant, was effectively warranting that the calcium hydroxide content of the slaked lime would not be below the cited figure.)
134. So, when one asks whether the Cristal waste can accurately be described as consisting entirely of a calcium based reaction waste from titanium dioxide production, the answer is demonstrably that it is.
135. The same cannot be said of the FCC waste. On the contrary, as we have said in paragraph 123 above, the essence of the process giving rise to the FCC waste was the neutralisation of the APCRs using the FC. In addition:
(1) a significant part of the APCRs consisted of material which was not calcium based; and
(2) the presence of that material was not attributable to the purpose of neutralising the [ferrous chloride] arising from titanium dioxide production.
Thus, whilst a calcium based reaction did occur in the course of the process which led to the FCC waste, it would be a misnomer to describe that calcium based reaction as amounting to the essence of the process. Consequently, the waste which arose as a result of the process did not consist entirely of a calcium based reaction waste from titanium dioxide production and the Cristal waste is readily distinguishable from the FCC waste.
136. It may be seen from the above that we emphatically reject the proposition that, because:
(1) the slaked lime used in the course of the process at Stallingborough is diluted in water so that only 20% of the virgin calcium hydroxide slurry consists of calcium hydroxide; and
(2) between 10% and 30% of the APCRs was reactive and most of the reactive compounds were calcium based,
the Cristal waste and the FCC waste must inevitably stand or fall together when it comes to determining whether or not they come within the ambit of Note (9)(a). The percentage of calcium hydroxide which is in the virgin calcium hydroxide slurry at Stallingborough is simply the result of the need to dilute the slaked lime appropriately so that the calcium based reaction which occurs in the process at Stallingborough neutralises the [ferrous chloride] from the titanium dioxide production without giving rise to a waste which is itself hazardous by virtue of its alkalinity. In contrast, the percentage of calcium hydroxide which is in the APCRs at FCC Knostrop was a function of the substantial other material of which the APCRs consisted, whose presence in the APCRs had nothing whatsoever to do with the calcium based reaction which occurred at FCC Knostrop.
Grounds of appeal
Ground 1 The FTT failed to correctly construe, and took into account irrelevant considerations in its application of, section 42(2) FA 1996 and Note 9(a) of the QMO ('the relevant statutory provisions').
Ground 2 The FTT erred in law in applying an "essence of the process" / "only purpose" test which is not contained in, and involves an impermissible gloss on, the relevant statutory provisions.
Ground 3 - The FTT erred in law in failing to construe the relevant statutory provisions purposively and /or failing to consider whether its construction and application of the relevant statutory provisions in particular its "essence of the process" / "only purpose" test was consistent with the underlying environmental objectives of section 42(2) FA 1996, the QMO and the Treasury criteria and / or produced a result which was inconsistent with those environmental objectives.
Discussion
15. In the task of ascertaining whether a particular statutory provision imposes a charge, or grants an exemption from a charge, the Ramsay approach is generally described - as it is in the statements quoted above - as involving two components or stages. The first is to ascertain the class of facts (which may or may not be transactions) intended to be affected by the charge or exemption. This is a process of interpretation of the statutory provision in the light of its purpose. The second is to discover whether the relevant facts fall within that class, in the sense that they answer to the statutory description (Barclays Mercantile at para 32). This may be described as a process of application of the statutory provision to the facts. It is useful to distinguish these processes, although there is no rigid demarcation between them and an iterative approach may be required.
16. Both interpretation and application share the need to avoid tunnel vision. The particular charging or exempting provision must be construed in the context of the whole statutory scheme within which it is contained. The identification of its purpose may require an even wider review, extending to the history of the statutory provision or scheme and its political or social objective, to the extent that this can reliably be ascertained from admissible material.
30. External aids to interpretation therefore must play a secondary role. Explanatory Notes, prepared under the authority of Parliament, may cast light on the meaning of particular statutory provisions. Other sources, such as Law Commission reports, reports of Royal Commissions and advisory committees, and Government White Papers may disclose the background to a statute and assist the court to identify not only the mischief which it addresses but also the purpose of the legislation, thereby assisting a purposive interpretation of a particular statutory provision. The context disclosed by such materials is relevant to assist the court to ascertain the meaning of the statute, whether or not there is ambiguity and uncertainty, and indeed may reveal ambiguity or uncertainty: Bennion, Bailey and Norbury on Statutory Interpretation, 8th ed (2020), para 11.2. But none of these external aids displace the meanings conveyed by the words of a statute that, after consideration of that context, are clear and unambiguous and which do not produce absurdity.
63. While all of this guidance is important, I emphasise in particular that (a) the words which Parliament has chosen to enact are "the primary source by which meaning is ascertained", for "the important constitutional reason" explained by Lord Nicholls in the Spath Holme case that citizens "should be able to rely upon what they read in an Act of Parliament"; (b) "[e]xternal aids to interpretation must therefore play a secondary role"; (c) no external aids can "displace the meanings conveyed by the words of a statute that, after consideration of that context, are clear and unambiguous and which do not produce absurdity"; and (d) "the intention of Parliament" is an objective concept in the sense lucidly explained by Lord Nicholls in Spath Holme [2001] 2 AC 349, 396.
108. The incantation of a purposive interpretation is of no avail, if the relevant words construed in their context, and with due regard to the statutory purpose, admit of only one meaning and do not produce absurdity
Material must be treated as qualifying material if it would in fact be such material but for a small quantity of non-qualifying material; and whether a quantity of non-qualifying material is small must be determined in accordance with the terms of the direction.
(1) A calcium based reaction did occur in the course of the process which led to the FCC Waste.
(2) A significant majority of the reactive compounds in the APCR were calcium based and they tended to be more reactive than the non-calcium based reactive compounds.
(3) It was common ground, as recorded at [71(3)] that the reactions giving rise to the FCC Waste were primarily between calcium compounds in the APCRs and the ferrous chloride.
(1) The slaked lime slurry contained only 10 20% calcium compounds and could contain reactive non-calcium compounds.
(2) It was unclear whether the water used to create the slurry contained reactive alkaline elements.
(3) The slurry produced by mixing the slaked lime slurry and the ferrous chloride contained solids originally existing in the ferrous chloride, solids precipitated during the reaction and unreacted calcium hydroxide.
(4) The filter cake produced by the process comprised 40 50% liquid by weight.
(1) The APCR contained relatively low levels of reactive material. At least 70% of the APCR did not react with the ferrous chloride.
(2) The reactive material in the APCR contained a significant proportion of non-calcium based compounds.
(3) Between 57% and 72% of the FCC Waste was neither reaction waste nor did it derive from titanium dioxide production.
(4) All this meant that a large quantity of APCR was required to neutralise the ferrous chloride. Some 3.9 tonnes of APCR were required to neutralise 1 tonne of ferrous chloride, compared to 260 kg of slaked lime powder.
(1) As the FTT noted at [131] to [133], there were "minimal impurities" in the slaked lime slurry used in the process to neutralise the ferrous chloride, and that the slurry contained site water which itself contained impurities. It found as a fact that these impurities were "unavoidable features of the process". The slaked lime powder consisted of at least 90% pure calcium hydroxide. We agree with the FTT that in those circumstances the existence of minimal impurities in the Cristal Waste did not cause the Cristal Waste to fall outside Note 9(a). Nor indeed did the existence of water in the slaked lime slurry and in the resulting Cristal Waste. The FTT found that the slaked lime was highly reactive and had to be diluted with water in order to carry out the calcium based reaction between the calcium hydroxide and the ferrous chloride. The water was a necessary part of the process and could properly be viewed as reaction waste.
(2) In contrast, at least 70% of the APCR played no part in the reaction with the ferrous chloride. There was no finding that this material was a necessary part of the process. Between 57% and 72% of the FCC Waste was neither reaction waste nor was it a necessary part of the process. Mr Nawbatt's submissions to the contrary were not supported by any finding of fact by the FTT. Further, the reactive material in the APCR contained a significant proportion of non-calcium based compounds.
(1) It was common ground that a waste did not need to be composed entirely of calcium reaction compounds. We acknowledge that not all the Cristal Waste comprised calcium reaction compounds because of the presence of impurities and water. However, the impurities and the water were unavoidable features of the process and fall within the term "calcium based reaction waste".
(2) The test we have applied focusses on the reactions which led to the waste.
(3) The reactions giving rise to the FCC Waste were primarily between calcium compounds in the APCR and the ferrous chloride. However, that does not mean that the FCC Waste fell within Note 9(a). The fact that at least 70% of the APCR did not react with the ferrous chloride and was not necessary for the process cannot be ignored.
Conclusion